Publications

OIPO Disability Abstracts: Artificial Intelligence, Machine Learning, and Virtual Reality

Updated 3/10/2025

Artificial Intelligence and Machine Learning

Binns, R., & Kirkham, R. (2021). How could equality and data protection law shape AI fairness for people with disabilities? arXiv – CS – Computers and Society. DOI: arxiv-2107.05704.

This article examines the concept of ‘AI fairness’ for people with disabilities from the perspective of data protection and equality law. This examination demonstrates that there is a need for a distinctive approach to AI fairness that is fundamentally different to that used for other protected characteristics, due to the different ways in which discrimination and data protection law applies in respect of Disability. We articulate this new agenda for AI fairness for people with disabilities, explaining how combining data protection and equality law creates new opportunities for disabled people’s organisations and assistive technology researchers alike to shape the use of AI, as well as to challenge potential harmful uses.

Goggin, G., Prahl, A., & Zhuang, K. V. (2023). Communicating AI and Disability. In  M. S. Jeffress, J. M. Cypher, J. Ferris, & J. Scott-Pollock (Eds.), The Palgrave Handbook of Disability and Communication (pp. 205-220). Cham: Palgrave Macmillan. DOI:  https://doi.org/10.1007/978-3-031-14447-9_13.

This chapter looks at a relatively new area of disability and communication: AI. It contends that discourses, language, and representation of disability in relation to AI need to be understood against the backdrop of evolving ideas of disability and technology. It critiques the dominant social imaginaries of AI and disability, which obscure the flaws in the mainstream ways that autonomous intelligent systems such as AI developed. The chapter concludes that AI and its dominant social imaginaries are in the throes of a severe crisis of legitimacy. Accordingly, alternative imaginaries are discussed as ways to reimagine and remake AI, machine learning, intelligent systems, and other technologies as sustainable, just, and conducive to the goals of extending accessibility, inclusion, participation, and rights for people with disabilities.

Jafry, A., & Vorstermans, J. (2024). Evolving intersections: AI, disability, and academic integrity in higher education. New Directions for Teaching and Learning Early View. DOI: https://doi.org/10.1002/tl.20629.

In this article, we investigate the critical intersections of AI, academic integrity, and disability in the context of a large undergraduate course. Our aim was to adapt the course to respond to generative AI (GenAI) to avoid entrenching barriers for students, and instead teach them how to use GenAI tools in ways that deepen their learning and uphold academic honesty. Grounded in disability justice and access pedagogies, we outline five design goals centered on guidelines for AI usage, education on responsible AI use, revised assessments, support for teaching assistants (TAs), and accessible materials. These activities are detailed in our methodology. In our findings, we provide a critical reflection of the course adaptation, taking up issues such as varying levels of familiarity with GenAI, students’ capacity to engage with course changes, resistance to GenAI, instructors’ relational shifts to AI, and feelings of demoralization among the teaching team. We conclude by offering practical recommendations for educators, calling for learning communities to view this disruption as an invitation to listen to disabled students.

Kohnke, S., & Zaugg, T. (2025). Artificial Intelligence: An Untapped Opportunity for Equity and Access in STEM Education. In L. Dieker, E. Vasquez., & M. T. Marino (Eds.), Application of AI Technologies in STEM Education [Special Issue]. Education Sciences15(1), 68. DOI: https://doi.org/10.3390/educsci15010068.

Artificial intelligence (AI) holds tremendous potential for promoting equity and access to science, technology, engineering, and mathematics (STEM) education, particularly for students with disabilities. This conceptual review explores how AI can address the barriers faced by this underrepresented group by enhancing accessibility and supporting STEM practices like critical thinking, inquiry, and problem solving, as evidenced by tools like adaptive learning platforms and intelligent tutors. Results show that AI can positively influence student engagement, achievement, and motivation in STEM subjects. By aligning AI tools with Universal Design for Learning (UDL) principles, this paper highlights how AI can personalize learning, improve accessibility, and close achievement gaps in STEM content areas. Furthermore, the natural intersection of STEM principles and standards with the AI4K12 guidelines justifies the logical need for AI–STEM integration. Ethical concerns, such as algorithmic bias (e.g., unequal representation in training datasets leading to unfair assessments) and data privacy risks (e.g., potential breaches of sensitive student data), require critical attention to ensure AI systems promote equity rather than exacerbate disparities. The findings suggest that while AI presents a promising avenue for creating inclusive STEM environments, further research conducted with intentionality is needed to refine AI tools and ensure they meet the diverse needs of students with disabilities to access STEM.

Lillywhite, A., & Wolbring, G. (2019). Coverage of ethics within the artificial intelligence and machine learning academic literature: The case of disabled people. Assistive Technology Online Before Print. DOI: https://doi.org/10.1080/10400435.2019.1593259.

Disabled people are often the anticipated users of scientific and technological products and processes advanced and enabled by artificial intelligence (AI) and machine learning (ML). Disabled people are also impacted by societal impacts of AI/ML. Many ethical issues are identified within AI/ML as fields and within individual applications of AI/ML. At the same time, problems have been identified in how ethics discourses engage with disabled people. The aim of our scoping review was to better understand to what extent and how the AI/ML focused academic literature engaged with the ethics of AI/ML in relation to disabled people.  Of the n = 1659 abstracts engaging with AI/ML and ethics downloaded from Scopus (which includes all Medline articles) and the 70 databases of EBSCO ALL, we found 54 relevant abstracts using the term “patient” and 11 relevant abstracts mentioning terms linked to “impair*”, “disab*” and “deaf”. Our study suggests a gap in the literature that should be filled given the many AI/ML related ethical issues identified in the literature and their impact on disabled people.”

Lillywhite, A., & Wolbring, G. (2020). Coverage of artificial intelligence and machine learning within academic literature, Canadian newspapers, and Twitter tweets: The case of disabled people. Societies, 10(3). DOI: https://doi.org/10.3390/soc10010023.

Artificial intelligence (AI) and machine learning (ML) advancements increasingly impact society and AI/ML ethics and governance discourses have emerged. Various countries have established AI/ML strategies. “AI for good” and “AI for social good” are just two discourses that focus on using AI/ML in a positive way. Disabled people are impacted by AI/ML in many ways such as potential therapeutic and non-therapeutic users of AI/ML advanced products and processes and by the changing societal parameters enabled by AI/ML advancements. They are impacted by AI/ML ethics and governance discussions and discussions around the use of AI/ML for good and social good. Using identity, role, and stakeholder theories as our lenses, the aim of our scoping review is to identify and analyze to what extent, and how, AI/ML focused academic literature, Canadian newspapers, and Twitter tweets engage with disabled people. Performing manifest coding of the presence of the terms “AI”, or “artificial intelligence” or “machine learning” in conjunction with the term “patient”, or “disabled people” or “people with disabilities” we found that the term “patient” was used 20 times more than the terms “disabled people” and “people with disabilities” together to identify disabled people within the AI/ML literature covered. As to the downloaded 1540 academic abstracts, 234 full-text Canadian English language newspaper articles and 2879 tweets containing at least one of 58 terms used to depict disabled people (excluding the term patient) and the three AI terms, we found that health was one major focus, that the social good/for good discourse was not mentioned in relation to disabled people, that the tone of AI/ML coverage was mostly techno-optimistic and that disabled people were mostly engaged with in their role of being therapeutic or non-therapeutic users of AI/ML influenced products. Problems with AI/ML were mentioned in relation to the user having a bodily problem, the usability of AI/ML influenced technologies, and problems disabled people face accessing such technologies. Problems caused for disabled people by AI/ML advancements, such as changing occupational landscapes, were not mentioned. Disabled people were not covered as knowledge producers or influencers of AI/ML discourses including AI/ML governance and ethics discourses. Our findings suggest that AI/ML coverage must change, if disabled people are to become meaningful contributors to, and beneficiaries of, discussions around AI/ML.

Morrison, R. J. (2019, Summer). Ethical depictions of neurodivergence in SF about AI. Configurations, 27(3), 387-410. DOI: https://doi.org/10.1353/con.2019.0021.

In science fiction (SF), representations of artificial intelligence (AI) run the gamut from being cognizant of the full spectrum of potential human emotion, to lacking any comparable emotional states. When a feeling/unfeeling AI—the novum of the text—interacts with human characters, the presence of strong emotional capability is shown to be positive, and any absence of emotional capability is shown to be negative, even abject. This aligns perceived emotional capability with normality, establishing that the empirical “zero world” of the text is one in which those who lack normative emotional affect lack value.

Mosha, N. F. (2025). The role of artificial intelligence tools in enhancing accessibility and usability of electronic resources in academic libraries. Library Management Ahead-of-Print. DOI: https://doi.org/10.1108/LM-08-2024-0088.

Purpose This study examined the role of artificial intelligence (AI) tools in facilitating the accessibility and usability of electronic resources (e-resources) in academic libraries.

Design/methodology/approach This study employed a quantitative descriptive survey to collect data from library users. The population targeted was sampled using a purposive sampling technique. A total of 427 (58%) participated in this study.

Findings Most respondents preferred electronic journals (e-journals) among the e-resources stored in academic libraries. Chatbots were identified as preferred AI tools for accessing and enhancing the usability of these resources. Strategies mentioned included the potential for integrating AI tools across various e-resources. However, among the challenges reported was the inability to integrate AI tools with the existing library management systems. Improving e-resource discovery and access can significantly enhance the effectiveness of AI tools in academic libraries.

Originality/value Originality in the context of AI applications in academic libraries refers to the unique approaches, innovative tools and creative solutions that enhance the accessibility and usability of electronic resources. By focusing on unique solutions that enhance the accessibility and usability of e-resources, these libraries can better serve their diverse user populations and adapt to the evolving landscape of information needs.

Newman-Griffis, D., Sage Rauchberg, J., Alharbi, R., Hickman, L., & Hochheiser, H. (2022). Alternative models: Critical examination of disability definitions in the development of artificial intelligence technologies. arXiv:2206.08287 [cs.AI]. DOI: https://doi.org/10.48550/arXiv.2206.08287.

Disabled people are subject to a wide variety of complex decision-making processes in diverse areas such as healthcare, employment, and government policy. These contexts, which are already often opaque to the people they affect and lack adequate representation of disabled perspectives, are rapidly adopting artificial intelligence (AI) technologies for data analytics to inform decision making, creating an increased risk of harm due to inappropriate or inequitable algorithms. This article presents a framework for critically examining AI data analytics technologies through a disability lens and investigates how the definition of disability chosen by the designers of an AI technology affects its impact on disabled subjects of analysis. We consider three conceptual models of disability: the medical model, the social model, and the relational model; and show how AI technologies designed under each of these models differ so significantly as to be incompatible with and contradictory to one another. Through a discussion of common use cases for AI analytics in healthcare and government disability benefits, we illustrate specific considerations and decision points in the technology design process that affect power dynamics and inclusion in these settings and help determine their orientation towards marginalisation or support. The framework we present can serve as a foundation for in-depth critical examination of AI technologies and the development of a design praxis for disability-related AI analytics.

Nugent, S. E., & Scott-Parker, S. (2022). Recruitment AI has a disability problem: Anticipating and mitigating unfair automated hiring decisions. In M. I. Aldinhas Ferreira & M. Osman Tokhi (Eds.), Towards Trustworthy Artificial Intelligent Systems [Intelligent Systems, Control and Automation: Science and Engineering Vol. 102]. (pp 85–96).

Artificial Intelligence (AI) technologies have the potential to dramatically impact the lives and life chances of people with disabilities seeking employment and throughout their career progression. While these systems are marketed as highly capable and objective tools for decision making, a growing body of research demonstrates a record of inaccurate results as well as inherent disadvantages for historically marginalised groups. Assessments of fairness in Recruitment AI for people with disabilities have thus far received little attention or have been overlooked. This paper examines the impacts to and concerns of disabled employment seekers using AI systems for recruitment, and discusses recommendations for the steps employers can take to ensure innovation in recruitment is also fair to all users. In doing so, we further the point that making systems fairer for disabled employment seekers ensures systems are fairer for all.

Packin, N. G., (2020, November 3). Disability Discrimination Using AI Systems, Social Media and Digital Platforms: Can We Disable Digital Bias?  SSRN. DOI: http://dx.doi.org/10.2139/ssrn.3724556.

Social media platforms and digital technological tools have transformed how people manage their day-to-day lives, socially as well as professionally. Big data algorithms help us improve our decision-making processes, and sophisticated social networks, enable us to get connected to other individuals and organizations, get exposed to information, and even learn about different opportunities. But as individuals come to be more and more comfortable with social networks and big data algorithms, fewer give much thought to how personal data gleaned from social networks and fed into algorithms affects the administration of government and the provision of private services. Algorithmic assessment of personal characteristics enables widescale discrimination by government and private entities, and such discrimination is particularly pernicious for persons with disabilities.

According to the social model of disability, disability is not only inherent to the individual and determined by the impairment but is also a product of the social environment. Social expectations, conventions, and technology determine which traits are outside the norm and which traits are disabling. Whether a technology perpetuates or mitigates disability depends on social norms, including norms that are embedded in law. A wheelchair might mitigate the impairment, but only if legal rules dictate a built environment where wheelchair users and non-wheelchair users can move in a similar fashion, can the disability be mitigated. Similarly, digital technologies can limit the ways in which some traits are disabling only if bias and discriminatory features against individuals with disabilities are not embedded within their use. We must ensure that technology developments continue to improve the life quality and opportunities for individuals with disabilities, and that we design systems that better accommodate the disabled, enhance their access, and help level the playing field between them and the able-bodied. We should regulate to ensure that individuals with disabilities are legally protected from discrimination. Additionally, and not less importantly, we must make sure that individuals with disabilities are not left out of innovations because of the difficulty in detecting the different types of disabilities as well as disability bias, proving it, and designing around it.

Parvin, N. (2019). Look up and smile! Seeing through Alexa’s algorithmic gaze. In K. Fritsch, A. Hamraie, M. Mills & D. Serlin (Eds.), Crip Technoscience [Special Section]. Catalyst, 5(1). DOI: https://doi.org/10.28968/cftt.v5i1.29592.

Echo Look is one latest product by Amazon built on the artificial intelligence agent Alexa designed to be a virtual fashion assistant. This paper draws on feminist theory to critically engage with the premises and promises of this new technology. More specifically, I demonstrate how the introduction of Echo Look is an occasion to think through ethical and political issues at stake in the particular space it enters, in this case no less than what is perceived of (women’s) bodies and what fashion is and does. In addition, the specific domain helps us see this category of technology anew, illuminating its taken-for-granted assumptions. More specifically, it serves as yet another reminder of what algorithms cannot do and of their oppressive potency.

Ringel Morris, M. (2020, June). AI and accessibility:  A discussion of ethical considerations [Viewpoint]. Communications of the ACM, 63(6), 35-37. DOI: https://doi.org/10.1145/3356727.

“According to the World Health Organization, more than one billion people worldwide have disabilities, the field of disability studies defines disability through a social lens; people are disabled to the extent that society creates accessibility barriers. AI technologies offer the possibility of removing many accessibility barriers; for example, computer vision might help people who are blind better sense the visual world, speech recognition and translation technologies might offer real time captioning for people who are hard of hearing, and new robotic systems might augment the capabilities of people with limited mobility. Considering the needs of users with disabilities can help technologists identify high-impact challenges whose solutions can advance the state of AI for all users; however, ethical challenges such as inclusivity, bias, privacy, error, expectation setting, simulated data, and social acceptability must be considered” (p. 35).

Robertson, S., Magee, L., & Soldatić, K. (2022). Intersectional inquiry, on the ground and in the algorithm. Qualitative Inquiry, 28(7), 814–826. DOI: https://doi.org/10.1177/10778004221099560.

This article makes two key contributions to methodological debates in automation research. First, we argue for and demonstrate how methods in this field must account for intersections of social difference, such as race, class, ethnicity, culture, and disability, in more nuanced ways. Second, we consider the complexities of bringing together computational and qualitative methods in an intersectional methodological approach while also arguing that in their respective subjects (machines and human subjects) and conceptual scope they enable a specific dialogue on intersectionality and automation to be articulated. We draw on field reflections from a project that combines an analysis of intersectional bias in language models with findings from a community workshop on the frustrations and aspirations produced through engagement with everyday artificial intelligence (AI)–driven technologies in the context of care.

Shew, A. (2020, March). Ableism, Technoableism, and Future AI. IEEE Technology and Society Magazine, 39(3), 40-85. DOI: https://doi.org/10.1109/MTS.2020.2967492.

Ableism (discrimination in favor of nondisabled people and against disabled people1) impacts technological imagination. Like sexism, racism, and other types of bigotry, ableism works in insidious ways: by shaping our expectations, it shapes how and what we design (given these expectations), and therefore the infrastructure all around us. And ableism shapes more than just the physical environment. It also shapes our digital and technological imaginations – notions of who will “benefit” from the development of Artificial Intelligence (AI) and the ways that those systems are designed and implemented are a product of how we envision the “proper” functioning of bodies and minds.

Smith, P., & Smith, L. (2021). Artificial intelligence and disability: Too much promise, yet too little substance? AI Ethics 1, 81–86. DOI: https://doi.org/10.1007/s43681-020-00004-5.

Much has been written about the potential of artificial intelligence (AI) to support, and even transform, the lives of disabled people. It is true that many advances have been made, ranging from robotic arms and other prosthetic limbs supported by AI, decision support tools to aid clinicians and the disabled themselves, and route planning software for those with visual impairment. Many individuals are benefiting from the use of such tools, improving our accessibility and changing lives. But what are the true limits of such tools? What are the ethics of allowing AI tools to suggest different courses of action, or aid in decision-making? And does AI offer too much promise for individuals? I have recently undergone a life changing accident which has left me severely disabled, and together with my daughter who is blind, we shall explore the day-to-day realities of how AI can support, and frustrate, disabled people. From this, we will draw some conclusions as to how AI software and technology might best be developed in the future.

Tilmes, N. (2022). Disability, fairness, and algorithmic bias in AI recruitment. Ethics and Information Technology, 24, Article 21.  DOI: https://doi.org/10.1007/s10676-022-09633-2.

While rapid advances in artificial intelligence (AI) hiring tools promise to transform the workplace, these algorithms risk exacerbating existing biases against marginalized groups. In light of these ethical issues, AI vendors have sought to translate normative concepts such as fairness into measurable, mathematical criteria that can be optimized for. However, questions of disability and access often are omitted from these ongoing discussions about algorithmic bias. In this paper, I argue that the multiplicity of different kinds and intensities of people’s disabilities and the fluid, contextual ways in which they manifest point to the limits of algorithmic fairness initiatives. In particular, existing de-biasing measures tend to flatten variance within and among disabled people and abstract away information in ways that reinforce pathologization. While fair machine learning methods can help mitigate certain disparities, I argue that fairness alone is insufficient to secure accessible, inclusive AI. I then outline a disability justice approach, which provides a framework for centering disabled people’s experiences and attending to the structures and norms that underpin algorithmic bias.

Trewin, S., Basson, S., Muller, M., Branham, S., Treviranus, J., Gruen, D., Hebert, D., Lyckowski, N., & Manser, E. (2019, September). Considerations for AI Fairness for People with Disabilities. AI Matters, 5(3), 40-63. DOI: https://doi.org/10.1145/3362077.3362086.

In society today, people experiencing disability can face discrimination. As artificial intelligence solutions take on increasingly important roles in decision-making and interaction, they have the potential to impact fair treatment of people with disabilities in society both positively and negatively. We describe some of the opportunities and risks across four emerging AI application areas: employment, education, public safety, and healthcare, identified in a workshop with participants experiencing a range of disabilities. In many existing situations, non-AI solutions are already discriminatory, and introducing AI runs the risk of simply perpetuating and replicating these flaws. We next discuss strategies for supporting fairness in the context of disability throughout the AI development lifecycle. AI systems should be reviewed for potential impact on the user in their broader context of use. They should offer opportunities to redress errors, and for users and those impacted to raise fairness concerns. People with disabilities should be included when sourcing data to build models, and in testing, to create a more inclusive and robust system. Finally, we offer pointers into an established body of literature on human centered design processes and philosophies that may assist AI and ML engineers in innovating algorithms that reduce harm and ultimately enhance the lives of people with disabilities.

Velazquez-Solis, P. E., González Correa, M. E., Martinez, M. A., Arroyo, J. G., & Marquez, M. Y. (2025). Designing teaching strategies using artificial intelligence for neurodivergent students in higher education. In M. Raygoza-L., J. Orduño-Osuna, A. Mercado-Herrera, R. Jimenez-Sanchez, & F. Murrieta-Rico (Eds.), Exploring psychology, social innovation and advanced applications of machine learning (pp. 191-208). New York: IGI Global Scientific Publishing. DOI: https://doi.org/10.4018/979-8-3693-6910-4.ch010.

Artificial intelligence (AI) can enhance teaching strategies for neurodivergent students in higher education. Neurodiversity, such as autism, ADHD, and dyslexia, needs tailored educational approaches often missing in traditional systems. As neurodivergent student enrollment rises, inclusive learning environments are essential. AI technologies offer personalized learning through adaptive platforms that adjust content based on real-time feedback, helping students tackle challenges and utilize their strengths. AI tools, such as emotion recognition, support mental health by detecting stress, frustration, or anxiety for timely interventions. A case study highlights integration of an AI-powered chatbot in a Color Theory course for Engineering students. The chatbot provided guidance and used visual aids, improving communication, independence, and confidence. Despite AI benefits, issues like over-reliance and digital divide must be considered. Developing empathetic AI solutions is crucial for supporting neurodivergent students, and collaboration among educators and researchers is essential.

White, J. J. G. (2022). Artificial intelligence and people with disabilities: A reflection on human–AI partnerships. In F. Chen & J. Zhou (Eds.), Humanity driven AI: Productivity, well-being, sustainability and partnership (pp 279–310). Springer, Cham. DOI: https://doi.org/10.1007/978-3-030-72188-6_14.

Artificial intelligence (AI) has much potential to enhance opportunities and independence for people with disabilities by addressing practical problems that they encounter in a variety of domains. Indeed, the partnership between AI and people with disabilities already has a history that spans several decades, through the use of assistive technologies based, for example, on speech recognition, optical character recognition, word prediction, and text-to-speech conversion. Contemporary developments in machine learning can extend and enhance the capabilities of such assistive technology applications, while opening the way to further improvements in accessibility. AI applications intended to benefit people with disabilities can also give rise to questions of values and priorities. These issues are here discussed in relation to the role of design practices and policy in shaping the solutions adopted. AI can also contribute to discrimination on grounds of disability, especially if machine learning algorithms are substituted partly or completely for human decision making. The potential for bias and strategies for overcoming it raise as yet unresolved research questions. In exploring some of these considerations, a case is developed for favoring approaches which shape the normative and social context in which AI technologies are developed and used, as well as the technical details of their design.

Virtual Reality

Brandt, M., & Messeri, L.  (2019). Imagining feminist futures on the small screen: Inclusion and care in VR fictions. In C. Bruun Jensen & A. Kemiksiz (Eds.), Anthropology and Science Fiction: Experiments in Thinking Across Worlds [Feature Issue]. Nature Culture Issue 5. https://www.natcult.net/journal/issue-5/imagining-feminist-futures-on-the-small-screen/.

Virtual reality signifies not only an immersive media technology, but also a cultural desire to allow bodies to inhabit other worlds as easily as pushing a button or putting on goggles. As the VR industry has grown, so too have popular imaginings of its potential. We draw on feminist technoscience studies to analyze and evaluate recent VR science fiction media narratives. How do they articulate VR’s role in the future, and for whom? Who are the heroes of these worlds and what makes them heroic? Steven Spielberg’s would-be blockbuster Ready Player One (2018) (RPO) offers a techno-masculine narrative in which a hero saves the world. In contrast to RPO, television and streaming small screen science fiction narratives have focused on the extent to which VR can save not worlds, but individuals. A surprisingly consistent trope has emerged in these shows: one of VR as a therapeutic tool for a woman coping with trauma. While certainly a departure from RPO’s Hollywood vision of VR, this analysis examines how episodes of Reverie, Philip K. Dick’s Electric Dreams, Kiss Me First, and Black Mirror offer visions of VR that reflect the feminist ambitions of the contemporary VR industry.

Jiang, Z., Meltzer, A., & Zhang, X. (2023). Using virtual reality to implement disability studies’ advocacy principles: Uncovering the perspectives of people with disability. Disability & Society. DOI: https://doi.org/10.1080/09687599.2022.2150601.

One central aim of disability studies is to shift understandings of disability, such that disability comes to be understood as about the social disadvantage/oppression that people face when society does not cater to impairment of body/mind. Nevertheless, there remains a need for more practical tools for disability advocacy, through which to transmit disability studies’ ideas of disability to the general community. Drawing on a qualitative study of the perspectives of 23 people with physical and sensory impairments, this paper proposes virtual reality as an advocacy tool to communicate the principles and beliefs of disability studies. The findings highlight that, due to the nature of the technology, participants feel virtual reality has clear potential as a disability advocacy tool that can facilitate empathy, perspective-taking and positive social change, with a particular focus on how it is the environmental barriers and social attitudes around people that disables them.

Redden, R. (2018, April 11). VR: An Altered Reality for Disabled Players. First Personal Scholar. Waterloo, ON: The Games Institute (GI) at the University of Waterloo in collaboration with IMMERSe, The Research Network for Video Game Immersion. Retrieved from: http://www.firstpersonscholar.com/vr-altered-reality/.

“…gather(s) the experiences and ideas of accessibility advocates who are working to inform VR’s trajectory. [The author is also]… providing..[a]… perspective of the VR station and its access. By putting existing ideas and experiences together, …[the author] hope[s] to promote the work that folks with disabilities are already doing in advising (and designing) games themselves, and the role of the public VR station in advocating and creating better VR” (n.p.)

Zhang, K., Deldari, E., Lu, Z., Yao, Y., & Zhao, Y. (2022). “It’s Just Part of Me:” Understanding Avatar Diversity and Self-presentation of People with Disabilities in Social Virtual Reality. In The 24th International ACM SIGACCESS Conference on Computers and Accessibility (ASSETS ’22), October 23–26, 2022, Athens, Greece. New York: ACM. DOI: https://doi.org/10.1145/3517428.3544829.

In social Virtual Reality (VR), users are embodied in avatars and interact with other users in a face-to-face manner using avatars as the medium. With the advent of social VR, people with disabilities (PWD) have shown an increasing presence on this new social media. With their unique disability identity, it is not clear how PWD perceive their avatars and whether and how they prefer to disclose their disability when presenting themselves in social VR. We fill this gap by exploring PWD’s avatar perception and disability disclosure preferences in social VR. Our study involved two steps. We first conducted a systematic review of fifteen popular social VR applications to evaluate their avatar diversity and accessibility support. We then conducted an in-depth interview study with 19 participants who had different disabilities to understand their avatar experiences. Our research revealed a number of disability disclosure preferences and strategies adopted by PWD (e.g., reflect selective disabilities, present a capable self). We also identified several challenges faced by PWD during their avatar customization process. We discuss the design implications to promote avatar accessibility and diversity for future social VR platforms.

OIPO Disability Abstracts: Eco-criticism

This literature review contains relevant material across several disciplines taking into account the interrelationship of the environment and disability, often referred to as “eco-crip theory” (Ray and Sibara, 2017). Included are books, articles, and other resources on topics such as:

  • Bioethics and biopolitics
  • The built environment and mapping for access
  • Climate justice and human rights
  • Crip eco-poetics
  • Crip ecology
  • Disability and animality
  • Disability and the environmental humanities
  • Eco-ableism
  • Environmental justice
  • Natural disasters, climate change, and migration
  • Nature, environment, and ecology
  • Recreation and leisure
  • Science and technology
  • Sustainable ecological systems
  • Urban environments and inaccessible spaces and places

Updated 9/23/2024

Abrahams, Y. (2018, Winter). How must I explain to the dolphins? An intersectional approach to theorizing the epistemology of climate uncertainty. In T. Glazebrook & A. Kola-Olusanya (Eds.), African Environmental Philosophy [Special Issue]. Environmental Ethics, 40(4), 389-404. DOI: https://doi.org/10.5840/enviroethics201840436.

The story of change and growth, i.e., evolution, in the traditional manner, involves an epistemology of indigenous knowledge systems that admits both evolution and the divine—and therefore the human capacity for free choice—that tells us that fossil fuels are a bad choice. Steven Biko’s message of “Black Consciousness” responds to the dilemma of how we belong to the species that is damaging the planetary ecosystem, amd yet how we can deny complicity by saying that reclaiming our culture enables us to see what we have done, so we can refuse complicity with the system that has divided us and take responsibility for giving birth to new life. The uncertainties of climate change can be thought through using race, class, gender, sexual orientation, indigeneity, and disability as categories of analysis. The result is an understanding that through both climate science and lived experience, we can know enough to know we ought to act on climate change. We do not need more research; we need instead an acceptance of our ignorance amid a sense of ethical responsibility

Alaimo, S. (2010). Bodily natures: Science, environment, and the material self. Bloomington, IN: Indiana University Press.

How do we understand the agency and significance of material forces and their interface with human bodies? What does it mean to be human in these times, with bodies that are inextricably interconnected with our physical world? Bodily Natures considers these questions by grappling with powerful and pervasive material forces and their increasingly harmful effects on the human body. Drawing on feminist theory, environmental studies, and the sciences, Stacy Alaimo focuses on trans-corporeality, or movement across bodies and nature, which has profoundly altered our sense of self. By looking at a broad range of creative and philosophical writings, Alaimo illuminates how science, politics, and culture collide, while considering the closeness of the human body to the environment.

Aldred, R., & Woodcock, J. (2008). Transport: Challenging disabling environments. In R. Imrie & H. Thomas (Eds.), The Environment and Disability: Making the Connections [Special Issue]. Local Environment, 13(6), 485-496. DOI: https://doi.org/10.1080/13549830802259847.

This article brings together the concerns of environmental and disability movements through examining the role of transport. Both movements critique current transport policy and practice. The disability movement has analysed how it marginalises the needs of disabled people, while environmentalists argue current transport trends are unsustainable and marginalise alternatives. Although these critiques operate independently and even seem opposed to each other, a common agenda can be developed through extending the social model of disability. The social model can be used to understand how car-dominated transport systems can be understood as disabling populations larger than those conventionally recognised as “disabled”. The car offers the technological fix of enabling abilities, in particular speed and strength, but in practice disables in a number of ways. Urban sprawl and traffic increase barriers to participation and access for many both ‘able-bodied’ and ‘disabled,’ while car dominance damages social interaction and limits sensory perception. Furthermore, the car economy is a major cause of impairment through crashes and physical inactivity. Understanding these together requires integrating the social model of disability with an eco-social model of impairment. This can show how unequal forms of social organisation are embodied in people and environments to produce patterns of impairment, disability and disadvantage. Finally we suggest policies to move towards sustainable societies with increased opportunities for broader social participation. The article argues that the two movements can create and benefit from a shared vision of socially inclusive, low-energy, sustainable transport.

Anderson, D. R. (2018). “This is the way I was”: Urban ethics, temporal logics, and the politics of cure. In K. Blanchard & C. Sandilands (Eds.), Sex and the (Motor) City: Ecologies of Middlesex [Special Forum]. The Goose: A Journal of Arts, Environment, and Culture in Canada, 17(1), Article 51.

This article employs Eli Clare’s concept of the ‘politics of cure’ in order to discuss issues of disability, temporality, and ethical relations to rehabilitation, restoration, and cure in the Sex and the (Motor) City: Ecologies of Middlesex special cluster. The special cluster compiles twelve short essays, originally presented in two linked roundtables at the Association for the Study of Literature and Environment (ASLE) conference in Detroit in June 2017, examining Jeffrey Eugenides’ 2002 Pulitzer Prize-winning novel, Middlesex.

Arathoon, J. (2022). Towards a research agenda for animal and disability geographies: Ableism, speciesism, care, space, and place. Social & Cultural Geography. DOI: https://doi.org/10.1080/14649365.2022.2152087.

Animal and disability geographies have become recognized fields of inquiry gaining traction with geographers of differing interests, approaches, and methods. To date, however, there has been limited engagement between the two fields themselves, despite healthy suggestions for such debate in the wider social sciences and humanities. This paper provides a series of provocations about the interconnections between animal and disability geographies to examine what they might add to each other, and why there is a need for (critical) work at this intersection. First, I suggest that animal and disability geographies share interconnections that encompass: their shared ontological challenges towards deconstructing speciesism and ableism respectively, and a growing focus on intersectional work. Second, I explore spaces of speciesist and disabling violence, arguing that thinking through these spaces will enable geographers to problematize and challenge ableism and speciesism. Third, I outline current engagement between the subfields, through the themes of space, place, and care. I argue that bringing the two together can build a stronger critical geography of justice by highlighting: i) ableism within animal studies, ii) speciesism within disability studies; and iii) the potential for constitutive relationships where both are brought to bear on issues and conceptual resources.

Armstrong, M., Sharaievska, I., B. M. Crowe, B. M., & Gagnon, R. J. (2022). Experiences in outdoor recreation among individuals with developmental disabilities: Benefits, constraints, and facilitators. Journal of Intellectual & Developmental Disability Online Before Print. DOI: https://doi.org/10.3109/13668250.2022.2104449.

Background: Individuals with developmental disabilities have specific physical and psychosocial needs that can require extra support to participate fully in and enjoy many benefits of recreation activities. Unfortunately, little is known about individuals with developmental disabilities’ experiences in outdoor recreation. The purpose of this study was to explore adults with developmental disabilities’ perceived benefits of outdoor recreation, and the conCramstraints or facilitators that affected their participation.

Method: Qualitative, semi-structured interviews were conducted with seven adults with developmental disabilities. Interviews were analysed using open, axial, and selective coding techniques.

Results: Results revealed three themes: (a) benefits of; (b) constraints to; and (c) facilitators of outdoor recreation. Benefits of outdoor recreation reported by study participants included their experiencing satisfaction, mental reprieve, empowerment, enlightenment, social connectedness, and thrill. Participants also shared intrapersonal, interpersonal, and structural constraints and facilitators related to their outdoor recreation participation.

Conclusions: Practical implications and future research recommendations are discussed.

Asamoah, P. G., Sanka, C. G., & Asafu-Adjaye, P. A. (2019, December). Mutualism and co-existence in Johanne Spyri’s Heidi.  Journal of Mother-Tongue Biblical Hermeneutics and Theology (MOTBIT), 1(2), 43-56. Article 4. DOI: https://doi.org/10.32051/12301904.

Reflections on the state of the environment and how some wish it to be are mirrored in the literary productions of some writers. The focus of this work is to analyze such a text as Heidi by Johanne Spyri which offers alternatives of survival which are mutualism and co-existence. Studies on Heidi have focused on other theories like psychoanalysis, however, none has looked at the text from an ecocritical perspective with mutualism and co-existence in mind. This work looks at the concept of mutualism and co-existence as metaphors from ecology. These metaphors are further sub-divided into other tropes which offer a better alternative way of life which are neither parasitic nor predatory, but positive symbioses. Using Heidi as the primary text, this purely qualitative study uses ecocritical tropes as an approach in tackling the relationship between humans and non-human aspects of the environment. The tropes used in this case are dwelling-, a geographical place and sense of belonging: animals, mutualism and co-existence with other humans; wilderness: the role of nature as a healer; and positive growth towards the good and the morally sound. The work recognizes that mutualism and co-existence in reality are underplayed in our world today and recommends a complete change-over of attitude towards the best possible way of living for both humans and non-humans within our environment.

Atkins, P. (2021). ‘All the living I have left to do’: A disability poetics of dwelling. In Z. Brigley, K. Evans & R. A. Mackenzie (Eds.), Dwelling [Feature Issue]. Magna 79.

We dwell in our bodies; our bodies in the world. Everything we experience of the world we experience in and through and with our bodies. Our relationship with our body informs our relationship with the world. For some people, this is easier to forget than for others. There are times I have wished I could relinquish tenancy of my body, and live easefully out with its structural issues, but it is my home on the earth.

Bares, A. (2019, Fall). “Each unbearable day”: Narrative ruthlessness and environmental and reproductive injustice in Jesmyn Ward’s Salvage the Bones. MELUS, 44(3), 21-40. DOI: https://doi.org/10.1093/melus/mlz022.

Jesmyn Ward’s 2011 novel Salvage the Bones tells the story of Esch Batiste and her family in the days leading up to Hurricane Katrina. Ward represents Esch’s unexpected pregnancy and the environmental degradation of her rural Mississippi Gulf Coast home as linked by the slow, quotidian forms of violence and risk exposure that characterize Jasbir K. Puar’s formulation of debility. Through scenes of reproductive and environmental injustice, Salvage the Bones elucidates the processes through which racially inflected political-economic systems unevenly produce debility in certain populations and environments while capacitating others. When put in conversation with critical race theory, critical disability theory, and environmental criticism, Salvage the Bones emphasizes the logics that underpin debility rather than sensationalizing or pathologizing its consequences. In its refusal to revert to ableist, racist literary codes and conventions, the novel theorizes and practices “narrative ruthlessness,” Ward’s description of her literary strategy to respond to debility’s representational conundrums of inevitability and invisibility. In so doing, narrative ruthlessness exceeds liberal humanist impulses to propose restoration, cure, or uplift as desirable solutions, insisting instead on kinship, care, redress, and salvage as possibilities for radical survival and futurity.

Bauman, W. A. (2015). Disability Studies, queer theory, and the new materialism: Environmental metaphors for a planet on the move. In J. W. Belser (Ed.), Religion, Disability, and the Environment [Special Issue]. Worldviews, 19(1), 69-73. DOI: https://doi.org/10.1163/15685357-01901005.

“In an exhibit by eco-artist Elizabeth Demaray at the 2014 meeting of the Association for Environmental Studies and Sciences in New York, the artist showcased a new project she is working on with engineer, Dr. Qingze Zou, entitled: `IndaPlant Project: An Act of Trans-Species Giving.’ In this project, the artist and engineer are working together to create ‘technologies’ for plants. The robotic ‘floraborgs’ allow houseplants to move freely in domestic settings in search of sunlight and water. These floraborgs are metaphors for some trans possibilities for future becomings of the planetary community. These hybrid formations, reminiscent of the moving trees known as ‘Ents’ in the Lord of the Rings trilogy, suggest the possibilities of interspecies communication and highlight the nature of life itself as assemblage. The authors in this issue of Worldviews bring disability studies and ecological thought together with queer theory, environmental justice and disaster studies. Since each article deals in some way with issues of hybridity and the possibilities for future becoming, the IndaPlant exhibit is a good place to begin reflecting on these intersecting (and at times conflicting) discourses. In this brief response, I suggest three important loci for the ongoing discussions of a nomadic ecology of planetary becoming, which derive from the three main articles in this issue: the intersections of queering nature, hybrid identities, and assemblages one can glean from disability studies; implications for thinking about the future of climate change; and the importance of what Rob Nixon (2011) calls the ‘geography of violence.’ Perhaps such a nomadic approach—what Sharon Betcher, following Jane Bennett, calls ‘vitalist materialism’—might help us deal better with the evolving multitude of the planetary community in ways that prevent us from narrowing multiple possibilities for becoming into singular movements toward progress” (p. 69).

Bell, S. L. (2019, June). Experiencing nature with sight impairment: Seeking freedom from ableism. Environment and Planning E: Nature and Space, 2(2), 304-322. DOI: https://doi.org/10.1177/2514848619835720.

The idea of nature as freedom has long captured the human imagination, particularly since the Romantic era when notions of escapism were underpinned by the idealisation and externalisation of nature. The drive for freedom persists in the findings of much contemporary research examining the contribution of nature to human health and wellbeing. Yet, this work tells us little about how cultural narratives of freedom play out in the lives of people living with impairment and disability, or the constraining ableist assumptions that often underpin popular discourses of nature. This paper aims to address this, drawing on the findings of an in-depth qualitative study exploring how 31 people with varying forms and severities of sight impairment, living in rural and urban areas of England, describe their experiences with(in) diverse types of nature through the life course. Moving beyond the ‘wilderness ideal’ and sensationalised ‘supercrip’ stories that reproduce ableist ideas of bodies without limitation, this paper foregrounds the richly textured ways in which participants experienced feelings of freedom with nonhuman nature. These freedoms are characterised as social, mobile and exploratory. In doing so, it seeks to make room for a range of nature experiences, folding social justice into the growing momentum to connect people with nature in the name of health and wellbeing.

Bell, S. L., Jodoin, S., Bush, T. N., Crow, L., Eriksen, S. H., Geen, E., Keogh, M., & Yeo, $. (2024). Beyond the single story of climate vulnerability. International Journal of Disability and Social Justice, 4(2), 48-70. DOI: https://doi.org/10.13169/intljofdissocjus.4.2.0048.

Health. Disability. Vulnerability. These words are often used when discussing the risks of climate disruption. These discussions warn of the potential for climate impacts to “undermine 50 years of gains in public health” (as stated by the Lancet Countdown on Climate Change). Increasingly, such discussions also acknowledge climate injustice, examining who will benefit or lose out from climate change, how and why. The embodied vulnerability of disabled people is often assumed within such discussions, with less consideration of the social, economic or political conditions that create this vulnerability.

By bringing disability justice and disability studies into correspondence with care, environmental and climate justice scholarship, this reflective paper challenges the master narratives that blur differentiated experiences of disability and climate impacts into a single story of inevitable vulnerability. Recognising disabled people as knowers, makers and agents of change, it calls for transformative climate action, underpinned by values of solidarity, mutuality and care.

Bell, S. L., Tabe, T., & Bell, S. (2019). Seeking a disability lens within climate change migration discourses, policies and practices. Disability & Society, 35(4), 682-687. DOI: https://doi.org/10.1080/09687599.2019.1655856.

Around 15% of the global population is estimated to live with disability. With the Millennium Development Goals failing to recognise disability issues, the Sustainable Development Goals seek to promote a stronger focus on the alleviation of poverty and inequality amongst disabled people. Since then, the vulnerability of disabled people has been highlighted within international climate change agreements. Yet a critical disability lens is largely lacking from broader aspects of climate change adaptation planning. Focusing primarily on examples from the Asia-Pacific region (a region including low-lying coastal areas and islands that are frequently highlighted as exemplars of communities on the front line of climate change), this article discusses the need to integrate critical insights from disability studies into current understandings of climate change adaptation and mobility if we are to facilitate more inclusive, democratic and equitable adaptation in the face of climate change.

Belser, J. W. (2015). Disability and the social politics of “natural” disaster: Toward a Jewish feminist ethics of disaster tales. In J. W. Belser (Ed.), Religion, Disability, and the Environment [Special Issue]. Worldviews, 19(1), 51-68. DOI: https://doi.org/10.1163/15685357-01901004.

The stories we tell about crisis and catastrophe often intensify structural violence, augmenting existing dynamics of racism, sexism, classism, and ableism. Disaster stories often reinforce cultural narratives of suffering womanhood and tragic stories of disability to portray people with disabilities—especially women—as “natural” and “inevitable” victims of a harsh new world. Examining both contemporary rhetoric in the wake of Hurricane Katrina and classical rabbinic Jewish narrative, I argue that tales of communities in crisis commonly depoliticize disaster. By inscribing the disabled body with a narrative of “natural” vulnerabilities and inevitable suffering, conventional disaster discourse obscures the political significance of structural inequalities that render people with disabilities more at risk in disaster. Bringing together disability studies scholarship and Jewish feminist ethics, I challenge the discursive tendency to portray disabled individuals as symbols of suffering—and to focus on the pathos of an individual in distress instead of critiquing social inequality. I advocate a constructive, redemptive storytelling that illuminates and critiques social and political exclusion, that underscores the agency and dignity of people in crisis, that valorizes the disability justice movement’s call for interdependence in community, and that captures the artistry and resiliency of disabled lives.

Belser, J. W. (2020, Fall). Disability, Climate Change, and Environmental Violence: The Politics of Invisibility and the Horizon of Hope. Disability Studies Quarterly, 40(4). DOI: https://doi.org/10.18061/dsq.v40i4.6959.

This article brings disability theory and activism into conversation with environmental justice, a conversation that has often been stymied by a fundamental difference in approaching disability. Environmental justice movements position disability as a visceral marker of environmental harm, while disability movements claim disability as a site of value and vitality, a position I call “disability embrace.” Rather than adjudicate these differences, I use them to pinpoint a barrier to political alliance: environmental disability is a consequence of structural violence. I argue that disability politics offer vital resources for grappling with climate change. Applying insights from disability studies and disability activism to the analysis of environmental damage reveals the political stakes of diagnosis—the way power contours how, when, and to what ends we recognize human and ecological impairment. Disability insights illuminate pervasive cultural patterns of invisibility and climate denial. Disability critiques of futurity and cure can also reconfigure the way we approach hope and help fashion a new narrative of what it might mean to live well in the Anthropocene.

Betcher, S. V. (2015). The picture of health: “Nature” at the intersection of disability, religion and ecology. In J. W. Belser (Ed.), Religion, Disability, and the Environment [Special Issue]. Worldviews, 19(1), 9-33. DOI: https://doi.org/10.1163/15685357-01901002.

“We carry our most intimate view of nature within our pictures of health. These images of health, often more amenable to ablenationalism than to a world of intra-active becoming, inform not only neoliberal policy, but ecological vision, including ecospiritualities. Increasingly “the politics of health” constitutes something like a structure of exclusion, a “racism that is biological” (Foucault). Since these intimate images of nature—these “pictures of health”—may be aggravating the next great planetary divide, disability studies might differently shape what we make of the picture of health, the “nature” that informs it, and a religious response to it. This article uses critical dis- ability studies to examine the ways in which the ideology of health, often motivating ecological concern and religious seeking, can coincidentally collude with neoliberal responsibilization and biotechnologically supported transhumanism, generating pol- icy enclosures of the gen-rich against the “refuse/d” or “waste/d.”

Bodies of Nature: Survival Lessons from Disabled Communities [Feature Issue]. (2021, Winter). Orion: People and Nature Magazine, 40(4).

IN THIS ISSUE, we gather a selection of writers and artists whose experiences broaden our understanding of sickness and disability, to foster a conversation among them about how the body informs our perception of and engagement with our surroundings. In “Age of Disability,” Sunaura Taylor follows a community threatened by toxic groundwater that fights ecological ableism. In “The Long View,” Sarah Capdeville faces autoimmunity and an ecosystem caught in chaos. Taylor Brorby lives with diabetes in the era of climate crisis in “In Range.” Marina Tsaplina tells the story of Dream Puppet, the poetic knowledges of ancient forests and disabled communities. Glenis Redmond writes about labor, lineage, and cancer. In “Retriever of Souls,” Amy Irvine’s daughter Ruby McHarg and her service dog navigate a forest of epilepsy. Enjoy columns by Lisa Wells, Meera Subramanian, Aimee Nezhukumatathil, and more. This issue is art directed by Georgina Kleege, a blind scholar who has consulted the Met and the Tate on access and equity.

Bowen, L. (2021, Summer). Learning to read ecologically: Disability, animality, and metaphor in Toni Morrison’s A Mercy. ELH, 88(2), 525-550. DOI: https://doi.org/10.1353/elh.2021.0020.

Metaphor has become somewhat unfashionable, as new materialist and non-symptomatic reading approaches have rightly championed the value of the literal in literary criticism. But does metaphorical interpretation necessarily empty its objects of their material stakes? This essay examines Toni Morrison’s engagement with metaphors of disability and animality, two categories whose associated scholarly fields have been especially critical of metaphor. The characters in A Mercy, who often read nonhuman animals and disabled humans metaphorically, model two methods of reading figurative bodies, which I term extractive and ecological. If we learn how to read bodies ecologically, metaphors need not flatten difference or material complexity, but can in fact make it more meaningful.

Calgaro, E. (2021). Climate disaster risk, disability, and resilience. Current History, 120(829): 320–325.
DOI: https://doi.org/10.1525/curh.2021.120.829.320.

This essay examines the everyday inequalities, stigmas, and injustices that leave people with disabilities highly vulnerable to escalating climate change risks. It argues that including people with disabilities in disaster risk reduction processes is essential to shaping inclusive, effective policies and practices. Examples of several programs that have done so are discussed. Focusing on the strengths of people with disabilities as resilient change-makers and as the experts in their own lives—instead of viewing them as dependent on others—can lead to the changes necessary to recognize their personal sovereignty and deliver disaster justice. Third in a series on disability rights around the world.

Campos, P. A. (2021, Fall). Disability panic and environmental advocacy. In Environmental Justice [Feature Issue]. Natural Resources & Environment, 36(2), 41-44.

Disability plays an important but often unrecognized role in environmental law. Attorneys can play a role in reducing bias against people with disabilities.

Castres, P. (2022, October 13). Climate policy and activism need to make space for disabled people. BMJ, o2387, 379. DOI: https://doi.org/10.1136/bmj.o2387.

In this commentary, the author makes salient points on how “Disabled people are disproportionately affected yet highly underrepresented by climate change, yet the disability community hasn’t been at the forefront of climate policy and activism,” a situation which needs to change.

Cella, M. J. C. (2013, Summer). The ecosomatic paradigm in literature: Merging disability studies and ecocriticism. Interdisciplinary Studies in Literature and Environment, 20(3), 574-596. DOI: https://doi.org/10.1093/isle/ist053.

“Th(e) deep entanglement—the dialectic of embodiment and emplacement—is the central subject of this essay as this dialectic forms the basis for what I call the ecosomatic paradigm. The ecosomatic paradigm assumes contiguity between the mind-body and its social and natural environments; thus, under this scheme, the work of negotiating a ‘habitable body’ and ‘habitable world’ go hand in hand” (pp. 574-575).

Cella, M. J. C. (Ed.). (2016). Disability and the environment in American literature: Toward an ecosomatic paradigm. Lanham, MD: Lexington Books.

This book includes a collection of essays that explore the relationship between Disability Studies and literary ecocriticism, particularly as this relationship plays out in American literature and culture. The contributors to this collection operate from the premise that there is much to be gained for both fields by putting them in conversation, and they do so in a variety of ways. In this manner, the collection contributes to what Joni Adamson and Scott Slovic have referred to as a ‘third wave of ecocriticism.’ Adamson and Slovic attribute the rise of this “third wave” to the richly diverse contributions to ecocriticism over the past decade by scholars intent on including postmodernism, ecofeminism, transnationalism, globalization, and postcolonialism into ecocritical discussions. The essays in Toward an Ecosomatic Paradigm extend this approach of this ‘third wave’ by analyzing disability from an ‘environmental point of view’ while simultaneously examining the environmental imagination from a disability studies perspective. More specifically, the goal of the collection is to investigate the role that literary narratives play in fostering the ‘ecosomatic paradigm.’ As a theoretical framework, the ecosomatic paradigm underscores the dynamic and inter-relational process wherein human mind-bodies interact with the places, both built and wild, they inhabit. That is, the ecosomatic paradigm proceeds from the assumption that nature and culture are meshed in an ongoing and deep relationship that has implications for both the human subject and the natural world. An ecosomatic approach highlights the profound overlap between embodiment and emplacement, and is therefore enriched by both disability studies and ecocritical insight. By drawing on points of confluence between disability studies and ecological criticism, the various ecosomatic readings in this collection challenge normative (even ableist) constructions of the body-environment dyad by complicating and expanding our understanding of this relationship as it is represented in American literature and culture. Collectively, the essays in this book augment the American environmental imagination by highlighting the relationship between disability and the environment as reflected in American literary texts across multiple periods and genres.

Chen, M. Y. (2012). Animacies: Biopolitics, Racial Mattering, and Queer Affect [Perverse Modernities: A Series].  Durham, NC:  Duke University Press.

In Animacies, Mel Y. Chen draws on recent debates about sexuality, race, and affect to examine how matter that is considered insensate, immobile, or deathly animates cultural lives. Toward that end, Chen investigates the blurry division between the living and the dead, or that which is beyond the human or animal. Within the field of linguistics, animacy has been described variously as a quality of agency, awareness, mobility, sentience, or liveness. Chen turns to cognitive linguistics to stress how language habitually differentiates the animate and the inanimate. Expanding this construct, Chen argues that animacy undergirds much that is pressing and indeed volatile in contemporary culture, from animal rights debates to biosecurity concerns. Chen’s book is the first to bring the concept of animacy together with queer of color scholarship, critical animal studies, and disability theory. Through analyses of dehumanizing insults, the meanings of queerness, animal protagonists in recent Asian/American art and film, the lead in toys panic in 2007, and the social lives of environmental illness, Animacies illuminates a hierarchical politics infused by race, sexuality, and ability. In this groundbreaking book, Chen rethinks the criteria governing agency and receptivity, health and toxicity, productivity and stillness—and demonstrates how attention to the affective charge of matter challenges commonsense orderings of the world.

Chen, M. Y. (2015). The reproduction in/of disability and environment. In J. W. Belser (Ed.), Religion, Disability, and the Environment [Special Issue]. Worldviews, 19(1), 78-92. DOI: https://doi.org/10.1163/15685357-01901007.

“What are the methods of disability studies when it works in the realm of environmental studies? Disability studies has long staked a practiced ambivalence toward medicalization and the deployment of science for ends of ‘health.’ Given this stance, what can be made of science’s overwhelming deployment within environmentalist discourses?” (p. 79)

Claasen, A., van den Eijenden, J., & Geurts, M. (2013, November). Transversal ecocritical praxis:  An interview with Patrick Murphy. Ecocriticsm [Feature Issue]. Frame: Journal of Literary Studies, 26(2), 101-112.

Dr. Patrick D. Murphy is a Professor and Chair of the Department of English at the University of Central Florida. He has authored Ecocritical Explorations in Literary and Cultural Studies (2009), Farther Afield in the Study of Nature Oriented Literature (2000), A Place for Wayfaring: The Poetry and Prose of Gary Snyder (2000), and Literature, Nature, and Other: Ecofeminist Critiques (1995). He has also edited or co-edited such books as The Literature of Nature: An International Sourcebook (1998) and Ecofeminist Literary Criticism and Pedagogy (1998). He is the founding editor of ISLE: Interdisciplinary Studies Literature and Environment. His ecocritical work has been translated into Chinese, Danish, Japanese, Korean, and Spanish. Frame conducted an interview with Murphy to learn more about his new book, Transversal Ecocritical Praxis (2013), and to discuss with him the field of ecocriticism in general.

Clare, E. (2015). Exile and pride: Disability, queerness, and liberation (3rd ed.). Durham, NC: Duke University Press.  DOI: https://doi.org/10.1215/9780822374879.

First published in 1999, Exile and Pride is essential to the history and future of disability politics. Eli Clare’s revelatory writing about his experiences as a white disabled genderqueer activist/writer established him as one of the leading writers on the intersections of queerness and disability and changed the landscape of disability politics and queer liberation. With a poet’s devotion to truth and an activist’s demand for justice, Clare unspools the multiple histories from which our sense of self unfolds. His essays weave together memoir, history, and political thinking to explore meanings and experiences of home. Here readers will find an intersectional framework for understanding how we actually live with the daily hydraulics of oppression, power, and resistance. At the root of Clare’s exploration of environmental destruction and capitalism, sexuality and institutional violence, gender and the body politic, is a call for social justice movements that are truly accessible to everyone.

Clare, E. (2017). Brilliant imperfection: Grappling with cure. Durham, NC: Duke University Press.

In Brilliant Imperfection, Eli Clare uses memoir, history, and critical analysis to explore cure—the deeply held belief that body-minds considered broken need to be fixed. Cure serves many purposes. It saves lives, manipulates lives, and prioritizes some lives over others. It provides comfort, makes profits, justifies violence, and promises resolution to body-mind loss. Clare grapples with this knot of contradictions, maintaining that neither an anti-cure politics nor a pro-cure worldview can account for the messy, complex relationships we have with our body-minds. The stories he tells range widely, stretching from disability stereotypes to weight loss surgery, gender transition to skin lightening creams. At each turn, Clare weaves race, disability, sexuality, class, and gender together, insisting on the nonnegotiable value of body-mind difference. Into this mix, he adds environmental politics, thinking about ecosystem loss and restoration as a way of delving more deeply into cure. Ultimately Brilliant Imperfection reveals cure to be an ideology grounded in the twin notions of normal and natural, slippery and powerful, necessary and damaging all at the same time.

Comer, T. A., & Junker, C. (2020). Disability Studies and Ecocriticism: Creative Critical Intersections [Special Thematic Volume]. Studies in the Humanities, 46(1-2).

This double journal issue of Studies in the Humanities is merely the most recent attempt to further the academic conversation occurring at the intersection of disability and ecology. In our call for papers we asked for essays focused on the following questions: What can be gained by investigating ecological issues through the lens of disability studies? What can be gained by investigating disability through the lens of ecocriticism? How can these two viewpoints be joined?

Articles published in this feature issue include an Introduction and the following:

  • On (Dis-)Ability and Nature in A Song of Ice and Fire
  • Ableism in Avatar: The Transhuman, Postcolonial Rapprochement to Bioregionalism
  • Ecstatic Others: Transcendent Mutant Bodies in Milligan and Allred’s X-Statix
  • Green Our Vaccines: Jenny McCarthy’s Environmentalist, Ableist Rhetoric
  • Eco-ability and the Corporeal Grotesque: Environmental Toxicity in Cherrie Moraga’s Heroes and Saints and Ambikasutan Mangad’s Swarga
  • The Ableist Human: Rethinking Agency with Ability through Max Frisch’s Man in the Holocene
  • Undoing Bodies: Tentacular Spaces and Sympoiesis in Octavia Butler’s Lilith’s Brood
  • Green Lovin’ Mamas Don’t Vax! The Pseudo-Environmentalism of Anti-Vaccination Discourse
  • Writing the Unruly Body: Disability, Femininity, and the Environment in Wallace Stegner’s Angle of Repose
  • Shimerda’s Ghost: Disability and the Myth of the Frontier in Great Plains Fiction

Cram, E., Law, M. P., & Pezzullo, P. C. (2022). Cripping Environmental Communication: A Review of Eco-Ableism, Eco-Normativity, and Climate Justice Futurities. Environmental Communication, 16(7), 851-863. DOI: https://doi.org/10.1080/17524032.2022.2126869.

The field of environmental communication has yet to integrate disability or ableism as a primary area of research or intersectional investment. The ableist silences and disability slights are notable, however. This review essay provides a working definition of eco-ableism, including a summary of disability imagined through medical and social models. Then, the authors reflect on the role of voice as a method. Next, the essay synthesizes existing interdisciplinary literature to establish three broad trajectories of environmental communication research: (1) ecoableism in wilderness and outdoor recreation; (2) eco-normativities in public health discourses; and (3) climate justice futurism as public advocacy. While not exhaustive, the authors hope this review essay will help prompt the overdue cripping of environmental communication.

Crock, M.E., McCallum AO, R.C. (2022). Disability, conflict, and environmental conditions – An Introduction. In M. H. Rioux, J. Viera, A. Buettgen, & E. Zubrow (Eds.), Handbook of disability. Springer, Singapore. DOI: https://doi.org/10.1007/978-981-16-1278-7_73-1.

It is now accepted that persons with disabilities suffer disproportionate harms in disaster and displacement contexts, most particularly when persons with disabilities cross international borders in search of protection. Advances in domestic and international laws and policies are changing attitudes and approaches for these people. However, achieving equal treatment and mainstreaming disability-inclusive and rights-based approaches to disaster risk management is a work in progress. The COVID-19 pandemic and ongoing conflicts around the world underscore the importance of the insights provided by the authors in this collection. The shared aim is to lay out a road map to ensuring the full and effective participation of all persons with disabilities in society, acknowledging the intersecting and cross-cutting issues that create barriers in contexts of disaster and displacement.

Dahlberg, A., Borgström, S., Rautenberg, M., & Sluimer, N. (2022, September). A Nearby Park or Forest Can Become Mount Everest. Access to Urban Green Areas by People in Wheelchair from an Environmental Justice Perspective: A Stockholm Case. In B. Plüschke-Altof & H. Sooväli-Sepping (Eds.), Whose Green City? Contested Urban Green Spaces and Environmental Justice in Northern Europe [Sustainable Development Goals Series Series (SDGS)] (pp. 19–40). Springer Nature Switzerland AG.

That green areas in rapidly urbanising landscapes are important for human well-being is well established. Parks, woodlands, nature reserves, street trees and backyards provide multiple benefits, e.g. through providing physical, mental, social, educational and cultural benefits. These effects should reach all ‘the people’. However, a precondition is accessibility, which has received growing research attention. The aim of this chapter is to contribute to this body of knowledge by presenting and discussing accessibility to urban nature from the viewpoint of people whose mobility is dependent on a wheelchair. Very few studies have focused on this group, and then primarily on physical access. We include a broader perspective on underlying factors affecting accessibility—juxtaposed with an environmental justice approach. Our exploration rests primarily on interviews with people dependent on a wheelchair and representatives of supporting organisations. To this is added data from an online survey. Our results highlight that access to urban green areas must be understood in a broad sense, e.g. where physical access includes the whole route from home and back again, and where mental and social access is equally crucial. Further, green areas include the whole spectrum from a window-view to an urban national park. The study sends valuable signals to planners, e.g. concerning and including people in wheelchairs in all stages of planning and maintenance.

Davey, C., & Tataryn, M. (Eds.). (2021). Disability Studies and Sustainable Ecology [Special Issue]. Sustainability, 13(17).

The accelerating climate crisis forces us to face current socio-economic inequalities and how crises disproportionately impact certain sectors of society. In many respects, the ongoing COVID-19 pandemic is a foreshadowing of how the burden of responding to a global crisis falls unequally. Other publications (e.g., Twig et al., 2011, Gartrel et al., 2020, Peek and Stough, 2010) explore how disabled people are disproportionately negatively affected by such crises. This is an injustice that must be remedied. Yet, in this Special Issue we want to consider the relationship between disability and sustainability from a different angle. Instead of just focusing on people with disabilities as a vulnerable group, and ecological changes as a risk, we want to explore how the conceptual thinking around disability in society interacts with the challenging rethinking of society that will be necessary for sustainability. We are asking: how can a critical perspective on disability, and a view of sustainability that incorporates the diversity inherent in disability, help guide us towards a future that incorporates a more holistic notion of interdependence and, hence, sustainability in our relationship with each other as humans but also with the natural world that surrounds and sustains us? This exploration of interdependence will indeed touch upon questions about our physical and social environments. How do we build our cities and communities? What can perspectives on disabilities teach us about what this says and/or determines about our relationships with each other and with our natural environments? What do different communities (i.e., indigenous people) have to offer in this regard? Finally, how can we conceptualize welfare for all in a way that does not depend on the exploitation of other people and the rest of the ecology?

Day, A. (2020). Crip Time and the toxic body: Water, waste and the autobiographical self. In F. Allon, R. Barcan, & K. Eddison-Cogan (Eds.), The Temporalities of Waste: Out of Sight, Out of Time (pp. 167-178). New York: Routledge. DOI: https://doi.org/10.4324/9780429317170.

Our relationship to climate change will vary depending on our proximity to fresh water and ocean water, poverty, illness and disability—a constellation of intersecting tensions that differentially deploy disaster and debility. This chapter explores three contemporary nonfiction writers, all of whom write of an intimate relationship with water and disability: Leah Laksmi Piepzna-Samarasinha’s Dirty River, Sandra Steingraber’s Living Downstream and Kristen Iversen’s Full Body Burden. Taken together, these three writers move us geographically across the United States, following the linear timeline of U.S. colonial occupation from Massachusetts to the American West, exploring eighteenth- and nineteenth-century industrial factory waste, nineteenth- and twentieth-century farm waste, and late twentieth-century nuclear waste. Focusing on the relationships Piepzna-Samarasinha, Steingraber and Iversen have to water and waste leads us to carefully consider the relationship of individual bodies to time and disability. Utilising a key conceptualisation in critical disability studies, Crip Time, this chapter explores how exposure to environmental toxins is a kind of slow violence enacted on the human body, causing us to think differently about cause and effect, contagion and illness, human debility and planet precarity.

Disability Inclusive Climate Action Research Program & International Disability Alliance. (2022, June). Disability Rights in National Climate Policies: Status Report. Disability Inclusive Climate Action. Montreal, PQ & New York: Research Program at the McGill Centre for Human Rights & Legal Pluralism and the International Disability Alliance.

Produced and released jointly by the Disability Inclusive Climate Action Research Program at
McGill University and the International Disability Alliance, this report provides a systematic
analysis of the inclusion of persons with disabilities and their rights in the climate commitments and policies adopted by State Parties to the United Nations Framework Convention on Climate Change (UNFCCC). Section 1 reiterates the key obligations owed by states to persons with disabilities under international law. Section 2 reviews whether and how States have recognized persons with disabilities and their rights in their communications to the UNFCCC and in their domestic climate adaptation and mitigation policies. Section 3 summarizes the key conclusions of our analysis and provide recommendations for enhancing disability inclusion in national climate policy-making. In the appendix to this report, we provide a compendium of references to disability from our dataset of domestic climate policies. (p. 2).

Duke Disability Alliance.  (2022). Jen Deerinwater: Accompliceship Now! Disability and Indigeneity on the Frontlines of Climate Crisis [YouTube Video]. Durham, NC: Duke University.

“How does climate crisis impact disabled and indigenous communities? What can we learn about resistance from crip wisdom and indigenous knowledges? Hear about the intersections of these topics from disabled Cherokee organizer and journalist, Jen Deerinwater.”

Eisen, N., Duyck, S., & Jodoin, S. (2019, December). The Rights of Persons with Disabilities in the Context of the UN Framework Convention on Climate Change: Relevant International Frameworks and Compilation of Decisions adopted by the Parties to the UNFCCC. Winnipeg, MB, Washington, DC, Council of Canadians with Disabilities (CCD), ONG Inclusiva, and Center for International Environmental Law (CIEL).

The Parties to the UN Climate Agreements have recognized that persons with disabilities are key stakeholders in the international response to climate change. As such, they must be engaged throughout the UNFCCC processes and their rights respected and promoted through any climate activity, including mitigation, adaptation, or capacity building. This document recalls the relevant provisions of the UN Convention on the Rights of Persons with Disabilities and of the Sendai Framework and provides a compilation of all references to persons with disabilities adopted by governments under the UN Framework Convention on Climate Change.

Engelman, A., Craig, L., & Iles, A. (2022, October). Global Disability Justice In Climate Disasters: Mobilizing People With Disabilities As Change Agents. In A. R. Weil (Ed.), Disability and Health [Feature Issue]. Health Affairs, 41(10), 1496-1504. DOI: https://doi.org/10.1377/hlthaff.2022.00474.

Disabled people are highly susceptible to climate change impacts and disasters, yet they often remain sidelined or largely invisible. Policy makers, humanitarian agencies, and governments need to address the climate-related vulnerabilities that disabled people encounter during acute events and in the course of more creeping forms of climate change. As deaf researchers, we call for integrating disability justice into climate and disaster preparedness policies and practices worldwide. A disability justice approach can embrace the strengths that disabled people bring to disaster planning and climate mitigation and advocacy efforts. In this article we present case studies from different global regions to illustrate how disability is overlooked in responding to climate-related health impacts and disaster planning. We also draw particular attention to mutual aid networks led by disabled people in adapting to climate-related health impacts. We then suggest questions to help policy makers and practitioners integrate disability justice into their work. Above all, disabled people, organizations, and service providers should take ownership over the process of developing policies and actions to better prevent, prepare for, and respond to climate disasters.

Eriksen, S. H., Grøndahl, R., & Sæbønes, A. (2021, December).On CRDPs and CRPD: why the rights of people with disabilities are crucial for understanding climate-resilient development pathways [Personal View]. Lancet Planetary Health, 5(12), e929-e939. DOI: https://doi.org/10.1016/S2542-5196(21)00233-3.

In this Personal View, we examine how the Convention on the Rights of Persons with Disabilities and lived experiences of disability can deepen understanding of four key features of climate-resilient development: social justice and equity as normative goals; the ethical underpinnings of social choices; the inequitable relations that drive marginalisation; and the ways in which society navigates uncertainty through inclusive and contestatory politics. A disability lens not only helps to understand how marginalisation generates vulnerability; it also helps to elaborate the ethic of solidarity as underpinning social choices and steering development towards climate-resilient pathways. Social justice concerns non-discrimination and equitable participation in everyday informal arenas, as well as formal decision making processes. The resilience knowledges of disabled people help to rethink sustainable development by expounding human interdependence and everyday problem solving in the face of uncertainties. They also contribute to opening up climate change decision making and knowledge processes in ways crucial to engendering transformative change. Embracing human diversity by recognising dignity and capacity is required to counter othering and marginalisation, ensure human wellbeing and planetary health, and achieve socially just development. As such, solidarity is not just a normative goal, but also a means of building climate-resilient development.

Fenney, D. (2017, August). Ableism and disablism in the UK environmental movement. Environmental Values, 26(4), 503-522. DOI: https://doi.org/10.3197/096327117X14976900137377.

This article considers disabled people’s involvement with the UK environmental movement. It draws on findings from qualitative research with disabled people in the UK exploring experiences of access to sustainable lifestyles. A number of experiences of disablism (the manifestation of oppression against disabled people) and ableism (assumptions and valorisations of non-disabled normality) were described. Similar issues were also identified in relevant documentary sources and from research into disabled people’s experiences in the context of other movements such as the wider anti-capitalist movement. These findings suggest that ableism may be a significant feature of the UK environmental movement. If this is the case, there are important implications for the wider success of this movement’s aims in terms of achieving environmental protection, as well as for the ongoing exclusion experienced by disabled people with regard to pro-environmental activities.

Fritsch, K., & McGuire, A. (2018, Spring). The Biosocial Politics of Queer/Crip Contagions [Special Issue]. Feminist Formations, 30(1).

“In this special issue, we chart the limits and possibilities of queer/crip biosocial politics by examining the ways these ideas intersect and commingle with the narratives, practices, and temporalities of contagion. Crip and queer mark out, and indeed, flaunt the failures of normativity. And, in their fierce assertion of the possibility of an outside or more-than-one, crip and queer share a striking range of political and imaginative affinities. Feminist scholars have variously theorized queer and crip as unsettling, strange, twisted, unintelligible, or disruptive (Ahmed 2006; Butler 1993; Kafer 2013; McRuer 2006; Muñoz 2009; Kuppers 2011; Sandahl 2003; Chen 2012; Puar 2012; Johnson 2015; Clare 2001; McRuer and Mollow 2012). Building upon and extending these insights, this issue traces the multiple and unexpected ways queer and crip influence and infect one another” (p. vii).

Fritsch, K., Hamraie, A., Mills, M., & Serlin, D. (2019). Special Section: Crip Technoscience. Catalyst: Feminism, Theory, Technoscience, 5(1). DOI: https://doi.org/10.28968/cftt.v5i1.

“This special section of Catalyst maps the central nodes of the emerging field of crip technoscience, which we situate at the intersection of feminist technoscience studies and critical disability studies. Crip technoscience marks areas of overlap between these fields as well as productive disciplinary and political tensions. Our section brings together critical perspectives on disability and science and technology in order to grapple with historical and contemporary debates related to digital and emerging technologies, treatments, risk, and practices of access, design, health, and enhancement” (pp. 1-2).

Global Action on Disability (GLAD) Network. (n.d.). Promoting Disability-Inclusive Climate Change Action. Geneva, Switzerland and New York, NY: Author.

The preamble to the 2015 Paris Agreement includes persons with disabilities as one of the populations most acutely affected by climate change. However, subsequent provisions omit disability inclusion as an essential principle in action against climate change.

Persons with disabilities remain largely excluded from decision-making processes and plans to address and prevent climate change and the responses to climate-related disasters and emergencies at sub-national, national, regional, and international levels. The inclusion of persons with disabilities is pivotal to ensuring that efforts to implement the UN Framework Convention on Climate Change (UNFCCC) and out comes of the Paris Agreement are inclusive. Conversely, persons and organizations of persons with disabilities must advocate for a holistic approach to disability inclusion.

To address this, the Secretariat of the GLAD Network, in close consultation with and guidance by the GLAD Network’s working group on disability-inclusive climate action, is pleased to present to you with an issue paper and guide to promoting disability-inclusive climate change as well as 3 Steps Toward Disability-Inclusive Climate Action.

Good, G. A. (2022). Guest Editorial: Disasters and Disability: A Call to Action. Journal of Visual Impairment & Blindness, 116(6), 761-763. DOI: https://doi.org/10.1177/0145482X221144405.

“In recent years, most people living on the planet have been affected by or have witnessed devastating disasters such as earthquakes, floods, hurricanes, and wildfires, not to mention the fact that we have all been living through the COVID-19 pandemic. As researchers and professionals who work with disabled people (in this editorial, I will use the language of the Social Model of Disability, which acknowledges that disability is socially imposed by society onto those living with impairments); as parents, family members, and friends of those living with disability; and as disabled persons ourselves, I am sure we have all been concerned about the safety and welfare of those we care about who are coping with these crises, emergencies, and disasters.

There are many potential disasters to prepare for, including natural disasters, human-made and industrial disasters, economic or state collapse, school shootings, and other emergencies. These crises affect people who are blind or have low vision and those with other impairments across the age spectrum, as well as their families, educators, practitioners, and the first responders, healthcare workers, policymakers, and stakeholders charged with leading a coordinated response to any disaster. It is clear that innovative research, effective policies, and practices are needed, along with a massive awareness campaign, so that visually impaired people, and those with other impairments, are not forgotten in the various stages of disasters and emergencies such as preparation, planning, response, and recovery” (p. 761).

Goodley, D. (2020). Challenging transhumanism: Clutching at straws and assistive technologies. Balkan Journal of Philosophy, XII(1), 5-16.

This paper cautiously ponders the offerings of transhumanism. We begin the paper by introducing the transhumanist movement and related transdisciplinary thinking before giving space to the emergence of critical disability studies. We argue that the latter field has the potential to ground a critical and reflexive analysis of transhumanism– not least through a consideration of the contributions of posthuman and green disability studies. Drawing on these two perspectives, two specific areas of transhuman contemplation are offered. First, we consider (in the section titled, ‘The Ban on Straws: Disability prosthetics and the complication of eco-politics’) the relationship between disability advocacy politics and the potential ableism present in popular eco-political discourse. Second, we explore mainstreaming assistive technologies and e-waste collateral. These analytical thematics highlight the complexities of a critical transhuman disability studies, not least, in relation to the clash of disability and green politics. We conclude the paper with some considerations for future theory and research that trouble an uncritical acceptance of transhumanism in the area of critical disability studies.

Goodrow, G. (2019). Biopower, disability and capitalism: Neoliberal eugenics and the future of ART regulation. Duke Journal of Gender Law & Policy, 26(139), 137-155.

Discourse around reproductive and contraceptive technology in the United States is typically organized around ideas of autonomy, privacy, and free choice. The dichotomy of ‘pro-choice’ and ‘pro-life’ structures all debates on the topic, and the political framework of neoliberalism channels discussion into prepackaged frameworks of cost-benefit analysis and the primacy of free market choice. However, an examination of history and present policy developments paints a different picture. This Note argues that access to and regulation around contraception, abortion, and overall reproductive health and technology has been informed by and continues to interact with ideas of biopower and both positive and negative eugenics, and that neoliberal conceptions of free reproductive choice ignore the implications of this connection. Part II traces the history of the eugenics movement in America, exemplified by forced and coerced sterilization of people considered mentally or physically ‘degenerate,’ particularly those confined to institutions, and explores the rhetoric in early contraceptive-focused treatises and court decisions that reflect eugenicist views. Part III analyzes the modern trends on legal access to and regulation of reproductive and contraceptive technology and its interaction with race, socioeconomic status, and, in particular, disability (one of the more anxiety-producing categories of humanity in the neoliberal era). In Part IV, the Note goes on to argue that construction of a rational and compassionate legal framework where a woman’s right to choose is preserved (or revived) and the humanity of disabled persons is also respected is not only possible, but essential. A truly feminist reproductive framework must be built on justice, not market choice, and must respect both the agency and autonomy of pregnant women and the humanity and individual subjectivity of disabled persons. Policy strategies towards this end will not be easy, but attention to all the intersectional and overlapping factors that affect women’s reproductive decision-making, especially with regard to disability and reproductive technology, can change the way we view and value disabled personhood in our society.

Gottlieb, R. S. (2015, January). Disability and environment: Cautions and questions. In J. W. Belser (Ed.), Religion, Disability, and the Environment [Special Issue]. Worldviews, 19(1), 74–78. DOI: https://doi.org/10.1163/15685357-01901006.

“The essays in this issue utilize and advance current thinking about intersections of environmental crisis, disability, politics, morality, and religion. They are passionate and creative, challenging both common sense and the theoretical status quo. They utilize resources from culture, philosophical critique, political movements, and current events. My critical comments are made in the same spirit as the essays themselves, and in appreciation for the authors’ intellectual accomplishments. I write as the father of a 28 year old daughter, Esther, who has multiple physical, neurological, and development disabilities” (p. 74).

Grassi, S. (2017). “Queer natures”: Feminist ecocriticism, performativities, and Ellen van Neerven’s “Water.”  LEA – Lingue e letterature d’Oriente e d’Occidente, 6, 177-192. DOI: https://doi.org/10.13128/LEA-1824-484x-22336.

This paper brings together queer ecological thought, ecofeminism, and feminist ecocriticism to explore forms of embodied resistance against intersectional, complex oppressions of women, races, and lands. It looks at the award-winning Indigenous Australian writer Ellen van Neerven’s short story, ‘Water’ (from the 2014 collection, Heat and Light) to canvas an anti-essentialised queer feminist politics and ethics of care through which to shape utopian futures after sovereignty, after the West, after patriarchy, after whiteness.

Grossman, S. J. (2019, May). Living lexicon for the environmental humanities: Disabilities. Environmental Humanities, 11(1), 242-246.  DOI: https://doi.org/10.1215/22011919-7349532.

In this brief entry, I give shape to the affective ties [between disability (visible and invisible) and ravaged environments] by exploring the relation between physical disability and ravaged environments as one of resonance and echo and not as a canonized history or a tested theory. I draw on my personal history, as well as emerging work in disability studies and environmental humanities, in order to literalize these resonances and echoes across nature-cultures” (p. 242).

Groulx, M., Freeman, S, & Lemieux, C. (2022, March). Accessible nature beyond city limits – A scoping review. Journal of Outdoor Recreation and Tourism, 37. DOI: https://doi.org/10.1016/j.jort.2022.10049.

The health and well-being benefits of nature contact are well known, but inequitably distributed across society. Focusing on the access needs of persons with a disability, the purpose of this study was to systematically examine research on the accessibility of nature-based tourism and recreation spaces outside of urban/community settings. Following a scoping review methodology, this study sought to examine policies, services, physical infrastructures, and regulatory standards intended to enable equitable use of nature-based settings by individuals of all ages and abilities, particularly persons with a disability. In total, 41 relevant studies were identified and analyzed. Findings indicate that there are considerable gaps in the provision of services and information that enable self-determination in the use and enjoyment of nature, and that accessibility in nature-based settings is conceptualized through three interrelated policy/design pathways: the adaptation pathway, the accommodation pathway, and the universal design pathway. As a whole, accessibility policy and standards research specific to natural settings outside of urban/community settings is highly limited.

Management implications: There are growing calls to promote inclusive nature experiences in tourism and recreation spaces outside of community settings. Management of such spaces must reconcile equity concerns with a host of other priorities like environmental conservation. In the case of promoting universal accessibility, few studies offer insight into the detailed standards that must be met to create barrier-free access, let alone how to integrate such standards with other management priorities. Transdisciplinary research partnerships that involve management personnel, environmental and public health researchers, and persons with a disability are needed to identify effective management synergies.

Grue, J., & Lundbad, M. (2019). The biopolitics of disability and animality in Harriet McBryde Johnson. In N. Watson & S. Vehmas (Eds.), Routledge Handbook of Disability Studies (2nd ed.) (pp. 117-126). New York and London: Routledge.

“This chapter represents a multidisciplinary and collaborative approach to an enduring problem in disability studies, namely the valuation of different lives and kinds of lives. The authors believe that this problem can be explored in interesting ways if disability studies and human animal studies interact more closely. Historically, the academic fields that study disability and animality have not been in close communication. In fact, their relationship can perhaps more accurately be described as being wary of the implications of findings in the other field. We feel, however, that communication – and collaboration – may turn out to be essential. This is partly because key problem areas that concern both fields, including the criteria according to which different lives are valued and what exactly constitutes a life that is worth protecting, are also approached through other lines of inquiry, including the neo-utilitarianism that is most closely associated with the philosopher and ethicist Peter Singer. In Singer’s approach (admittedly simplified), capacities for higher cognitive functions and for suffering often become the major criteria that are deployed across species boundaries in order to determine the relative value of different beings, and thereby the lives of many animals and disabled people are potentially devalued. The 2002 debate between Singer and Harriet McBryde Johnson, one of the major disability activists of her generation, is one of the points of departure for this chapter. In a much vaunted encounter at Princeton University, USA, Johnson defended the intrinsic value of the lives of human beings with disabilities, while effectively refusing to countenance Singer’s position that species boundaries cannot by themselves constitute grounds for distinguishing between different forms of life. In this chapter, we delve deeper into what lies beneath the Singer-Johnson encounter, along with Johnson’s other writing, to consider the broader issues at stake. The chapter is structured as a dialogue. This reflects our desire not to conflate or artificially collapse animality studies and disability studies into a single disciplinary endeavour, but rather to find those areas and problems to which both fields have something important to contribute. We hope that the text will read not as a debate, but as an exploratory conversation with the shared purpose of finding out what disability studies and animality studies can teach each other, as well as other disciplines” (p. 117).

Hall, K. Q. (2014). No failure: Climate change, radical hope, and queer crip feminist eco-future. Radical Philosophy Review, 17(1), 203-225. DOI: https://doi.org/10.5840/radphilrev201432614.

This paper offers a critique of the emphasis on anti-futurity and failure prevalent in contemporary queer theory. I argue that responsibility for climate change requires commitments to futures that are queer, crip, and feminist. A queer crip feminist commitment to the future is, I contend, informed by radical hope.

Hamraie, A. (2018). Enlivened city: Inclusive design, biopolitics, and the philosophy of liveability. Built Environments, 44(1), 77-104. DOI: https://doi.org/10.2148/benv.44.1.77

Shortly after the United States announced its withdrawal from the Paris climate accords, mayors of global cities committed to addressing climate change via urban-scale projects aimed at promoting liveable, sustainable, and healthy communities. While such projects are taken for granted as serving the common good, this paper addresses the ideological dimensions of planning liveable cities with health promotion in mind. Liveability, I argue, is a normative ideology wherein liveliness and activation perform affective roles, associating urban design methods with feel-good imagined futures while rendering built structures as polemics against disabled and racialized populations. Using Nashville, Tennessee, a mid-sized US city, as a case study, the paper parses the progressive vision of the liveable city from the ideologies, political economies, and development practices that simultaneously activate some lives while excluding others.

Hamraie, A., & Fritsch, K. (2019). Crip technoscience manifesto. In K. Fritsch, A. Hamraie, M. Mills, & D. Serlin (Eds.), Special Section on Crip Technoscience. Catalyst: Feminism, Theory, Technoscience, 5(1), 1-34. DOI: https://doi.org/10.28968/cftt.v5i1.29607.

As disabled people engaged in disability community, activism, and scholarship, our collective experiences and histories have taught us that we are effective agents of world-building and -dismantling toward more socially just relations. The grounds for social justice and world-remaking, however, are frictioned; technologies, architectures, and infrastructures are often designed and implemented without committing to disability as a difference that matters. This manifesto calls attention to the powerful, messy, non-innocent, contradictory, and nevertheless crucial work of what we name as ‘crip technoscience,’ practices of critique, alteration, and reinvention of our material-discursive world. Disabled people are experts and designers of everyday life. But we also harness technoscience for political action, refusing to comply with demands to cure, fix, or eliminate disability. Attentive to the intersectional workings of power and privilege, we agitate against independence and productivity as requirements for existence. Instead, we center technoscientific activism and critical design practices that foster disability justice.

Hart, D. (2022). Finding the Weight of Things: Larry Eigner’s Ecrippoetics. University of Alabama Press.

Larry Eigner (1927–1996) wrote thousands of poems in his lifetime, despite profound physical limitations caused by cerebral palsy. Using only the thumb and index finger of his right hand, Eigner generated a torrent of urgent and rich language, participating in vital correspondences as well as publishing widely in literary magazines and poetry journals.

While Eigner wrote before the emergence of ecopoetics, his poetry reflected a serious engagement with scientific writing and media, including Rachel Carson’s seminal Silent Spring. Eigner was writing about environmental disasters and climate change long before such concerns took on a moral incumbency. Similarly, Eigner was ahead of his time in his exploration of disability. The field of disability studies has expanded rapidly in the new millennium. Eigner was not an overtly biographical poet, at least as far as his physical limitations were concerned, but his poetry spoke volumes on the idea of embodiment in all its forms.

Finding the Weight of ThingsLarry Eigner’s Ecrippoetics is the first full-length study of Eigner’s poetry, covering his entire career from the beginning of his mature work in the 1950s to his last poems of the 1990s. George Hart charts where Eigner’s two central interests intersect, and how their interaction fueled his work as a poet-critic—one whose work has much to tell us about the ecology and embodiment of our futures. Hart sees Eigner’s overlapping concerns for disability, ecology, and poetic form as inextricable, and coins the phrase ecrippoetics here to describe Eigner’s prescient vision.

Hemingway, L., & Priestly, M. (2014). Natural hazards, human vulnerability and disabling societies: A disaster for disabled people?  Review of Disabiilty Studies, 2(3).

The policy and research literature on disaster management constructs disabled people as a particularly “vulnerable group.” In this paper, we combine concepts from disaster theory and disability theory to examine this assumption critically. Drawing on primary, secondary and tertiary sources, we assess the vulnerability of disabled people in two globally significant disasters: Hurricane Katrina in August 2005 and the Asian tsunami of December 2004. In both cases, disabled people were adversely affected in terms of their physical safety and access to immediate aid, shelter, evacuation and relief. Using a social model analysis we contest the view that this vulnerability arises from the physical, sensory or cognitive limitations of the individual and show how it may be attributed to forms of disadvantage and exclusion that are socially created. The paper concludes that “natural hazards” are realised disproportionately as “human disasters” for disabled people, and most notably for disabled people in poor communities. Social model approaches and strong disabled people’s organisations are key to building greater resilience to disaster amongst “vulnerable” communities in both high-income and low-income countries.

Heylighen, A. (2008). Sustainable and inclusive design: A matter of knowledge? In R. Imrie & H. Thomas (Eds.), The Environment and Disability: Making the Connections [Special Issue]. Local Environment, 13(6), 531-540. DOI: https://doi.org/10.1080/13549830802259938.

In analysing parallels between sustainable and inclusive design, the paper investigates reasons for architects’ disappointing uptake of these approaches so far. A common reason seems to be the lack of knowledge that has the applicability required by architectural practice. Researchers produce knowledge on why and how we should accomplish more sustainable practices in building, which rarely filters down to practicing architects. Vice versa, the knowledge developed through architects’ design experiences rarely feeds back into academic research. Moreover, in the case of inclusive design, the user side represents a valuable body of knowledge as well: through their specific interaction with buildings/spaces, users with disabilities appreciate qualities and detect misfits most architects are unaware of. If the uptake of sustainability and inclusiveness in architecture is to be improved, the major challenge thus seems less a need to generate more knowledge than a need to make more effective use of what is already available.

Hickman, L. N. (2015). Lead me beside still waters: Toxic water, Trisomy 21 and a theology of eco-social disability. In J. W. Belser (Ed.), Religion, Disability, and the Environment [Special Issue]. Worldviews, 19(1), 34-50. DOI: https://doi.org/10.1163/15685357-01901003.

Artist Ena Swansea paints a provocative paradox in ‘One’ from her ‘4 Seasons’ quadtych: Is the child in the bathtub playfully holding a bubble, the orb of our global commons, or a crystal ball that portends an ominous future? As the viewer is confronted with the image of a child who, in the middle of an ordinary daily routine, is up to his armpits in a pool of blood red water, the question of water toxicity becomes central in the painting. Working from that image, this paper explores the interaction between water toxicity and Trisomy 21, proposing the need for a ‘precautionary principle’ to guide decisionmaking. The rationale for that principle is developed here through a study of communities with heightened links between water toxicity and Trisomy 21, a deepened theology of water across worldviews drawing on the work of John Hart’s Sacramental Commons, and a proposed model for ‘eco-social disability.’ Because scientific studies linking toxic water and Trisomy 21 are inconclusive, the precautionary principle serves as a guide to prevent the potential disabling effects of toxic water causing unjust generation of disablement.

Hilton, E. (2022, May). Building a more inclusive climate movement: Climate change and disabilities. Journal of Environmental Health, 84(9), 34-36.

In November 2021, world leaders gathered at the 26th United Nations Climate Change Conference of the Parties (COP26) to discuss global climate policy and the urgent need to address harmful emissions that arc accelerating global warming and extreme weather events devastating communities worldwide. Given the importance of this event and the need to hear from diverse voices, it was disappointing that the Israeli Energy Minister Karine Elharrar could not attend the first day of discussions because she uses a wheelchair and the meeting venue was not accessible. Climate change is accelerating with visible impacts around the world. Climate change can also cause increased disease and worsened physical, mental, and community health conditions. Exacerbating the outsized impact of climate change factors on people with disabilities is the fact that actions being pursued by those in the environmental and environmental justice movements can be at odds with the needs of people with disabilities.

Hughes, B. (2019). The abject and the vulnerable: The twain shall meet: Reflections on disability in the moral economy. The Sociological Review Monographs, 67(4), 829-846. DOI: https://doi.org/10.1177%2F0038026119854259.

The meaning of impairment is often Janus-faced. On the one hand, it is associated with defect, deformity, monstrosity and other tropes that carry the weight of ontological ruin, haunting narratives of physical, mental or sensory catastrophe that disturb the normate sense of being human. Impairment is invested with the debilitating social and moral consequences that symbolise disability. Disavowed and repudiated by the non-disabled community, disability represents the murky, shadow side of existence that separates normal embodiment from its benighted, abject ‘other’. Disgust – on the part of non-disabled, ‘clean and proper’ subjects – is the likely emotional response to the pollution and impropriety that disability represents. The emotional relation between the two parties may be mired in normate repulsion.

Humalisto, N. (2022) Generative spaces of climate change adaptation: Focus on disability inclusion. In H. Katsui & V. Mesiäislehto (Eds.), Embodied inequalities in disability and development (pp. 13-34). Stellenbosch, South Africa: African Sun Media. DOI: https://doi.org/10.52779/9781991201812

Climate change increases livelihood vulnerability and exposure to risks around the globe, but these impacts are not equally distributed among different people and places. Among the disadvantaged are persons with disabilities but their inclusion in projects and planning for climate change adaptation is low. Nepal is a challenging but typical context in the global South, where persons with disabilities have limited capacities to demand their basic rights, from secure livelihoods to sanitation, to be respected. Concurrently, (localised) institutions might not have the capacity to protect their constitutional rights. Consequently, while Nepalese policy encourages disability inclusion in adaptation planning, doing so in practice faces manifold political, cultural and social barriers. This chapter examines the conditions for inclusive adaptation based on ethnographic data from development projects run by seven Nepalese NGOs. The results show that demographic governance needs to be enhanced, and that the accountability of state institutions must co-evolve with the resilient livelihood opportunities for persons with disabilities. Inclusive adaptation hinges on creating trade-offs and positive feedback looks by generating opportunities for communal participation, refining evidence for circulation, and enabling scalar linkages between stakeholders and duty-bearers. 

Hyatt, B. (2021, August 18). Disability-Inclusive Local Climate Action Planning in the United States. Vibrant Environment Blog [Website]. Washington, DC: Environmental Law Institute.

“In order to protect people with disabilities from the worst impacts of climate change, local planners must build disability-inclusive climate action plans that draw upon lessons learned domestically from previous natural disasters and from abroad. They must take decisive steps to ensure the active participation of people with disabilities in the climate action planning process. If carried out effectively, these actions will save lives.”

Iengo, I. (2022). Endometriosis and environmental violence: An embodied, situated ecopolitics from the Land of Fires in Campania, Italy. Environmental Humanities, 14(2), 341–360. DOI: https://doi.org/10.1215/22011919-9712412.

This toxic autobiography seeks to open the conversation around the intersecting injustices marking the epistemological, material, political, and porous entanglements between endometriosis, the bodily inflammatory chronic condition the author is affected by, and the toxic waste fires raging in the territory known as the Land of Fires, between the provinces of Naples and Caserta, in southern Italy. Thinking with the sprouting intersection of environmental humanities and disability justice, while rooted in a critical environmental justice and transfeminist standpoint, the article uncovers the toxic embodiment where bodies and places are enmeshed. Although a growing body of literature acknowledges the role of chemical buildup and endocrine-disrupting toxins in the occurrence of endometriosis, the author delineates the epistemic injustices that keep this relationship silent in mainstream medical discourses. Through the blend of environmental memoir, embodied knowledge, activist campaigns, and medical literature, the article exposes the accumulation of environmental, medical, ableist, misogynist, and capitalist slow violence that living with endometriosis brings about. While emerging from the materiality of experiencing trauma and pain, the article reclaims the emancipatory possibilities that can be articulated. From the politicization of an “invisible” illness standpoint, the article proposes a toxic autobiography in which transfeminist, environmental, and disability justice politics are collectively affirmed through situated ecopolitics of response-ability that accounts for interdependence and self-determination of marginal bodies and territories.

Iengo, I., Kotsila, P., & Nelson, I. L. (2023). Ouch! eew! blech! A trialogue on porous technologies, places and embodiments. In W. Harcourt, A. Agostino, R. Elmhirst, M. Gómez, & P. Kotsila (Eds.), Contours of feminist political ecology: Gender, development and social change. Palgrave Macmillan, Cham. DOI: https://doi.org/10.1007/978-3-031-20928-4_4.

In this chapter, we bring political ecologies of health and the body into conversation with environmental justice and crip theory, science, technology and society studies (STS) and biopolitics. We present a trialogue that highlights three cases of health and embodiment examining the crosscutting themes of porosity and technologies as they offer us ways to insist on the right to be and signal a politics of health in FPE: (a) the lived experience of chronic pain as a catalyst for learning about environmental injustice in Naples, southern Italy, and the epistemic activism of crip communities producing counter-knowledge and mutual aid; (b) the spread of malaria among immigrant farmworkers in southern Greece as invisibilised intersectional and embodied injustice; and (c) embracing pharmaceuticals and vlogs with ambivalence while living with the temporary condition, hyperemesis gravidarum (HG) in the northeastern United States. We bring to the fore questions around bodies, harm, care and power, as those were brought about by our own situatedness in, and response-ability towards, embodied experiences of chronic pain, infection and nausea.

Ignagni, E., Chandler, E., Collins, K., Darby, A., & Liddiard, K. (2019, June). Designing access together: Surviving the demand for resilience. In K. Aubrecht & N. La Monica (Eds.), Survivals, Ruptures, Resiliences: Perspectives from Disability Scholarship, Art and Activism [Special Issue]. Canadian Journal of Disability Studies, 8(4), 293-320. DOI: https://doi.org/10.15353/cjds.v8i4.536.

Together we engaged in a project to co-design and co-create a fictional near-future world that would enable us to interrogate our present techno-social dilemmas.  Accessibility was central to our workshop for the way that access is always central to enacting crip, mad, Deaf, and spoonie communities. Without access, we cannot meet, discuss, share, struggle, fight, dismantle or create. Crucially, access was tied to our desire to co-create crip near-futures.

Imgrund, M. (2018, August 8). Eco-ableism: What it is, what it matters and how it affects disabled people. Eco Warrior Princess [Website/Blog].

Blog post defining and discussing “eco-ableism” in response the author’s research into environmental activism and calls to ban plastic straws, without considering the consequences to disabled people.

Imrie, R., & Thomas, H. (2008) Guest editorial: The interrelationships between environment and disability. In R. Imrie & H. Thomas (Eds.), The Environment and Disability: Making the Connections [Special Issue]. Local Environment, 13(6), 477-483. DOI: https://doi.org/10.1080/13549830802259748.

“This issue of Local Environment contributes to the process of bridging the gulf between the two social movements and sets of substantive and theoretical concerns, which, we argue, have much to learn from, and contribute to, each other. Inevitably, this collection of papers touches on a selective sub-set of issues, often suggesting scope for further research. In particular, they identify, and take forward, themes of dependence/community, or how disabled people are able to forge ways of changing environmental contexts; the role of experts and their knowledge; and the development of policy-related tools to facilitate environmental learning and change. The papers highlight that a great deal remains to be done to map and relate the discussions in the sprawling cross- disciplinary literatures that are characteristic of both environmentalism and disability” (pp. 478-479).

International Disability Alliance. (n.d.). Towards COP26: Enhancing Disability Inclusion in Climate Action [Disability Inclusive Climate Action COP26 Advocacy Paper]. New York and Geneva: Author.

“This document highlights the disproportionate impact of climate change and the possible adverse impacts of climate mitigation and adaptation activities on persons with disabilities. It also proposes measures to ensure the inclusion and participation of persons with disabilities and their representative organisations in climate-related decision-making” (p. 1).

Jacobs, N. A. (2022). Disability and ecofeminist literature. In D. A. Vakoch (Ed.), The Routledge Handbook of Ecofeminism and Literature (pp. 301-310). New York: Routledge. DOI: https://doi.org/10.4324/9781003195610-30.

This chapter explores the generative interconnections that unite ecofeminist literature and theory with disability studies and justice. Defining humans’ relationship with nature, not through a framework of esthetics—clean beaches and untouched forest land—but rather through an acknowledgment of differential living and working conditions based upon class, race, gender, location, and accessibility, ecofeminism has much to contribute to the realm of disability theory and activism. Moreover, transnational and feminist of color disability studies, in particular, advance invigorating possibilities for ecofeminism, especially in the framing of precarious lives. Ranging from early modern insights on both religious and scientific notions of corporeality to readings of contemporary fantasy, the representative works examined in this chapter reimagine disability through narratives of the bodymind. It examines the teratological —the “wondrous” or hybrid humanoid birth—and connections to animals and nonhuman nature in order to center disability within ecofeminist literature.

Jampel, C. (2018). Intersections of disability justice, racial justice and environmental justice. Environmental Sociology, 4(1), 122-135. DOI: https://doi.org/10.1080/23251042.2018.1424497.

This paper argues that environmental justice (EJ) scholarship, activism and policy that aims to ‘be intersectional’ by definition needs to include disability and ableism and, moreover, will benefit from specifically considering disability as a category of analysis. Incorporating intersectionality into EJ work means considering the implications of intersectional theory for collective liberation, for explanations of the sources and consequences of multiple systems of oppression and for theorizing connections among related justice struggles. This paper first takes each of these in turn, providing an explanation of what constitutes an intersectional approach. It then demonstrates how a disability justice approach further enriches ongoing work at the intersections of EJ and racial justice.

Jandrić, P,. & Ford, D. R. (Eds.). (2022). Postdigital ecopedagogies: Genealogies, contradictions, and possible futures [Postdigital Science and Education Series] (pp 3–23). Springer. DOI: https://doi.org/10.1007/978-3-030-97262-2.

This book conceptualizes ecopedagogies as forms of educational innovation and critique that emerge from, negotiate, debate, produce, resist, and/or overcome the shifting and expansive postdigital ecosystems of humans, machines, nonhuman animals, objects, stuff, and other forms of matter. Contemporary postdigital ecosystems are determined by a range of new bioinformational reconfigurations in areas including capitalism, imperialism, settler-colonialism, and ontological hierarchies more generally. Postdigital ecopedagogies name a condition, a question, and a call for experimentation to link pedagogical research and practice to challenges of our moment. They pose living, breathing, expanding, contracting, fluid, and spatial conditions and questions of our non-chronological present. This book presents analyses of that present from a wide spectrum of disciplines, including but not limited to education studies, philosophy, politics, sociology, arts, and architecture.

Jodoin, S., Ananthamoorthy, N., & Lofts, K. (2020). A Disability Rights Approach to Climate Governance. Ecology Law Quarterly, 47(1) 73-116. DOI: http://dx.doi.org/10.15779/Z38W37KW48.

Despite international recognition of the greater vulnerability of persons with disabilities to climate change, disability issues have received little attention from practitioners, policy makers, and scholars in this field. As countries move forward with measures to combat climate change and adapt to its impacts, it is critical to understand how these efforts can be designed and implemented in ways that can respect, protect, and fulfill the human rights of disabled persons. Drawing on the human rights model of disability enshrined in the United Nations Convention on the Rights of Persons with Disabilities, we set out a disability rights approach to climate governance that identifies the differential impacts of climate change for disabled persons and outlines the principles, obligations, and standards for designing and adopting accessible climate mitigation and adaptation policies and programs. On the whole, we argue that States should identify and pursue synergies between the realization of disability rights and the pursuit of initiatives to decarbonize their economies as well as prepare their societies against future climate impacts. In addition to fulfilling the rights of persons with disabilities and fostering a more inclusive world, disability-inclusive climate solutions can have resonant outcomes that can enable a greater share of the population to contribute to the emergence of carbon neutrality and enhance the climate resilience of society as whole.

Jodoin, S., Buettgen, A., Groce, N., Gurung, P., Kaiser, C., Kett M et al. (2023). Nothing about us without us: The urgent need for disability-inclusive climate research. PLOS Climate, 2(3), e0000153. DOI: https://doi.org/10.1371/journal.pclm.0000153.

“Around the world, disability communities are becoming increasingly vocal in calling attention to the ways in which they are disproportionally affected by climate change and the need to ensure that disability rights are respected, protected, and fulfilled in climate solutions [1,2]. As we will explain in this opinion, one key element of this emerging agenda for disability-inclusive climate justice is the need for in-depth and participatory action research on the intersections of disability and climate change.”

Kafer, A. (2005). Hiking boots and wheelchairs: Ecofeminism, the body, and physical disability. In B. S. Andrew J. C. Keller, & L. H. Schwartzmann (Eds.), Feminist interventions in ethics and politics: Feminist ethics and social theory (pp. 131-150). Lanham, MD: Rowman.

“In this essay, I trace the ways in which ecofeminisms—theories and practices that link the oppression of women and other marginalized groups to the degradation of nature–continue the repudiation of disability that occurs in mainstream discourses about the environment. Most ecofeminist analyses of difference and marginalization, for example, neglect to incorporate examinations of disability oppression, and the issue of disability access is rarely raised. Moreover, many ecofeminist accounts of nature are predicated on an assumption of the nondisabled body, enacting an implicit theoretical disavowal of disability and disabled bodies. Ecofeminisms tend to assume that an engagement with nature requires a deep immersion experience in nature, and that such an immersion experience requires a nondisabled body. There appears to be no room within ecofeminism for the disabled body” (p. 132).

Kafer, A. (2013). Bodies of nature: The environmental politics of disability. In Feminist, queer, crip (pp. 129-148). Bloomington: Indiana University Press.

‘Although concern with the environment has long been an animating force in disability studies and activism, “environment” in this context typically refers to the built environment of buildings, sidewalks, and transportation technologies. Indeed, the social model of disability is premised on concern for the built environment, stressing that people are disabled not by their bodies but by their inaccessible environments. (The wheelchair user confronting a flight of steps is probably the most common illustration of this argument.) Yet the very pervasiveness of the social model has prevented disability studies from engaging with the wider environment of wilderness, parks, and nonhuman nature because the social model seems to falter in such settings. Stairs can be replaced or supplemented with ramps and elevators, but what about a steep rock face or a sandy beach? Like stairs, both pose problems for most wheelchair users, but, argues Tom Shakespeare, “it is hard to blame the natural environment on social arrangements.” He asserts that the natural environment—rock cliffs, steep mountains, and sandy beaches—offers proof that “people with impairments will always be disadvantaged by their bodies”; the social model cannot adequately address the barriers presented by those kinds of spaces. I, too, recognize the limitations of the social model and the need to engage with the materiality of bodies, but I am not so sure that the “natural environment” is as distinct from the “built environment” as Shakespeare suggests. On the contrary, the natural environment is also “built”: literally so in the case of trails and dams, metaphorically so in the sense of cultural constructions and deployments of “nature,” “natural,” and “the environment.” Disability studies could benefit from the work of environmental scholars and activists who describe how “social arrangements” have been mapped onto “natural environments” (pp. 129-130).

Kälin, W. (2022). Disaster and climate change-induced displacement of persons with disabilities: A human rights perspective. In M. H. Rioux, J. Viera, A. Buettgen, & E. Zubrow (Eds.), Handbook of disability. Springer, Singapore. DOI: https://doi.org/10.1007/978-981-16-1278-7_27-1.

Disasters and adverse effects of climate change may significantly exacerbate pre-existing vulnerabilities of persons with disabilities. This is particularly true if such persons are displaced within their country or across borders. The systematic promotion and mainstreaming of disability-inclusive and rights-based approaches to disaster risk management and climate action are crucial to mitigate these challenges. The human rights of persons with disabilities which remain applicable during disasters and the principles of non-discrimination and equality of opportunity, participation and inclusion, accessibility, and reasonable accommodation help in shaping disability-inclusive measures to prevent displacement as well as the provision of protection and assistance during displacement. Finally, including persons with disabilities in programs and projects on durable solutions and ensuring their participation in decisions aimed at ending their displacement are crucial to avoid replicating and rebuilding barriers and ensuring their full and effective participation in society.

Kenney, M. (2019). Fables of response-ability: Feminist science studies as didactic literature. In K. Fritsch, A. Hamraie, M. Mills, & D. Serlin (Eds.), Special Section on Crip Technoscience. Catalyst: Feminism, Theory, Technoscience, 5(1), 1-39.  DOI: https://doi.org/10.28968/cftt.v5i1.29582.

Recent literature in feminist science studies is rich with stories about how we are constituted by and in relation to (sometimes toxic) chemicals. Scholars such as Natasha Myers, Mel Chen, and Eva Hayward have written vivid accounts of the chemical ecologies of late industrialism, arguing that we cannot think of bodies as separate from environments. In this article, I read feminist scholarship on chemical ecologies as fables of responseability, stories that teach us to attend and respond within our more-than-human world. Amplifying their didactic registers, I pay attention to moments in the texts that are speculative, poetic, and personal, moments that work on the bodies, imaginations, and sensoria of their readers. By reading these texts together, I hope to both acknowledge the didactic work that feminist science studies scholars are already doing and encourage others to experiment with telling their own fables of response-ability.

Kett, M., Sriskanthan, G., & Cole, E. (2021, December). Disability and Climate Justice: A Research Project. New York: Open Society Foundations.

“We commissioned this report in order to learn more about the interconnections between climate and disability, and to listen to practitioners on the ground around the world, with the aim of developing a set of recommendations to move the agenda of reciprocal engagement forward” (p. 4).

Kim, E. (2019). Continuing presence of discarded bodies: Occupation harm, necroactivism, and living justice. In K. Fritsch, A. Hamraie, M. Mills, & D. Serlin (Eds.), Special Section on Crip Technoscience. Catalyst: Feminism, Theory, Technoscience, 5(1), 1-31. DOI: https://doi.org/10.28968/cftt.v5i1.29616.

This essay explores the coexistence of struggles against the foreclosure of disabled people’s lives and against occupational illness, debilitation, and deaths caused by the manufacturing process of electronics in South Korea. Starting from the two activist campsites set up in Seoul and the historical backgrounds of occupational health movement, I draw on two documentary films, The Empire of Shame (2014) and Factory Complex (2015), that depict workers who became ill and those who died due to toxic exposure at semiconductor manufacturing plants. Beyond commemoration, necro-activism emerges in the form of persistent involvements of dead bodies, mourning, and objects representing death as important agents for making claims for justice. Taking into account political and historical differences of locations in which disabled people are positioned differently in the global order redirects us from the language of worth toward sociality, collective reframing of suffering and disability, and justice as an ongoing practice of everyday life and afterlife.

King, M. M., & Gregg, M. A. (2022, January). Disability and climate change: A critical realist model of climate justice. Sociology Compass, 16(1), e12954. DOI: https://doi.org/10.1111/soc4.12954.

Existing literature on climate change as an issue of environmental justice documents the heightened vulnerability of people with disabilities to the effects of climate change. Additionally, there are numerous studies showing that access to information is a prerequisite for perceiving risk and taking action. Building on this work, our review seeks to understand how physical disability relates to perceptions of climate-related risk and adaptations to climate-related events. We introduce a critical realist model of climate justice to understand the relationships between the environmental features that disable, risk perception and information seeking, and adaptive capacity and resilience to climate change. In understanding the vulnerability and adaptive capacity of people with disabilities to climate change, this review synthesizes research on one of the U.S.’s largest minority communities with the goals of better understanding how vulnerable populations cope with climate change and integrating them into climate action and policy.

King, M. M., Gregg, M. A., Martinez, A. V., & Pachoud, E. Y. (2022). Teaching & learning guide for disability and climate justice. Sociology Compass, 16(6), e12986. DOI: https://doi.org/10.1111/soc4.12986.

“Disability is widespread: nearly one in four Americans has a disability (Taylor, 2018) and disability cuts across demographic categories. Among individuals aged 15 and over, 12.6% had some type of mobility disability; above age 65, it is nearly 40% (Brault, 2012). Mobility disabilities heighten vulnerability to climate change and climate-related disasters (UNHCHR, 2020). Reduced information resources and mobility, increased health risks, and a lack of visibility in climate change discourse put people with disabilities in a more vulnerable position in the climate crisis. However, this vulnerability can be mitigated through relevant and sufficient access to information, risk mitigation strategies, and policy-shaping power. However, when these resilience-building resources are not accessible to disabled people, it exacerbates their vulnerability to climate change and becomes an issue of climate (in)justice. This guide and the accompanying  article explore ways to teach the intersection of disability and climate justice for a better understanding of each.”

Kosanic, A., Petzold, J. Martın-Lopez, B., & Razanajatovo, M. (2022, April). An inclusive future: Disabled populations in the context of climate and environmental change. In O. P. Dube, V. Galaz & W. Solecki (Eds.), Open Issue 2022 [Themed Issue]. Current Opinion in Environmental Sustainability, 55(101159). DOI: https://doi.org/10.1016/j.cosust.2022.101159.

Climate and environmental change impacts are projected to increase, constituting a significant challenge for meeting the Sustainable Development Goals (SDGs) while disproportionately affecting disabled populations. However, current research lacks knowledge on context-specific impacts of climate and environmental change on disabled populations. We use the environmental justice perspective that emphasises distributional, recognitional, and procedural dimensions regarding disabled populations to understand impacts and adaptation concerns and their implications for achieving the SDGs.

Kuppers, P.  (2022). Eco Soma: Pain and Joy in Speculative Performance Encounters [Art After Nature Series]. Minneapolis: University of Minnesota Press.

In Eco Soma, Petra Kuppers asks readers to be alert to their own embodied responses to art practice and to pay attention to themselves as active participants in a shared sociocultural world. Reading contemporary performance encounters and artful engagements, this book models a disability culture sensitivity to living in a shared world, oriented toward more socially just futures.

Eco soma methods mix and merge realities on the edges of lived experience and site-specific performance. Kuppers invites us to become moths, sprout gills, listen to our heart’s drum, and take starships into crip time. And fantasy is central to these engagements: feeling/sensing monsters, catastrophes, golden lines, heartbeats, injured sharks, dotted salamanders, kissing mammoths, and more. Kuppers illuminates ecopoetic disability culture perspectives, contending that disabled people and their co-conspirators make art to live in a changing world, in contact with feminist, queer, trans, racialized, and Indigenous art projects. By offering new ways to think, frame, and feel “environments,” Kuppers focuses on art-based methods of envisioning change and argues that disability can offer imaginative ways toward living well and with agency in change, unrest, and challenge.

Traditional somatics teach us how to fine-tune our introspective senses and to open up the world of our own bodies, while eco soma methods extend that attention toward the creative possibilities of the reach between self, others, and the land. Eco Soma proposes an art/life method of sensory tuning to the inside and the outside simultaneously, a method that allows for a wider opening toward ethical cohabitation with human and more-than-human others.

This text is also available via Open Access on the University of Minnesota Press website. As noted on the press’s website, “Retail e-book files for this title are screen-reader friendly with images accompanied by short alt text and/or extended descriptions.”

Lacayo, A. (2022). Of Toxic Dust and Sad Places: Ecochronicity and Debility in Julio Hernández Cordón’s Polvo (Dust, 2012). In S. Rust, S. Monani, & S. Cubitt (Eds.), Ecocinema Theory and Practice 2. New York: Routledge. DOI: https://doi.org/10.4324/9781003246602-15.

Julio Hernández Cordón’s Polvo (Dust) is a 2012 fiction film that recounts the impossibility of shooting a documentary about the victims of the Guatemalan Civil War (1960–1996). What gets in the way of filming is dust itself, which debilitates the protagonists with allergies, migraines, and insomnia. This chapter argues that Polvo revisits the war’s legacy by interweaving disability and environmental concerns through ecochronicity—the process through which bodies become chronically debilitated in toxic environments. Working at the intersection between disability studies and the environmental humanities, this chapter develops the notion of ecochronicity from contemporary debates about the chronic. Examining ecochronicity in light of Elizabeth Freeman’s definition of the chronic as a state of endurance, Mel Y. Chen’s conceptualization of how toxicity circulates among bodies and debilitates them, and Heather I. Sullivan’s dirt theory, this chapter considers the political and ecological dimensions of dust, articulating the way in which Polvo instantiates a “dirty” aesthetics. In Polvo, an ecochronicity is carried out in the aftermath of war and its legacies of violence: dust disables weak bodies, fertilizer acts as a toxin, and the Mayan Highlands remain a nonhuman casualty of war.

Landorf, C., Brewer, G., & Sheppard, L. A. (2008). The urban environment and sustainable ageing: Critical issues and assessment indicators. In R. Imrie & H. Thomas (Eds.), The Environment and Disability: Making the Connections [Special Issue]. Local Environment, 13(6), 497-514. DOI: https://doi.org/10.1080/13549830802259896.

Later life is a diverse experience but for some it is associated with a variety of impairments that impact on quality of life. Attention to date has focused on supporting ageing in place through modification to the home environment to compensate for increasing levels of impairment. This paper explores a further link between later life and the environment beyond the home. In doing so, the paper argues that the disabling impact of the urban environment on older people should be an essential consideration in the urban sustainability debate. A multi-dimensional framework combining sustainable development and ageing in place criteria is used to test the extent to which three sustainable urban environment assessment tools address the issue. The findings suggest that the capacity of an urban environment to support ageing in place is not being assessed as an integral element of a sustainable urban environment. Identifying factors that influence healthy later life will allow the inclusion of a later-life perspective in future urban sustainability planning and assessment models.

Leonard-Williams, H. (2024). Disability and climate anxiety. In J. Anderson, T. Staunton, J. O’Gorman, & C. Hickman (Eds.),
Being a therapist in a time of climate breakdown. London: Routledge. DOI: https://doi.org/10.4324/9781003436096-13.

My experiences of climate anxiety deeply intersect with my experiences of disability and ill health. Due to the ableism we face at every level of society, disabled people are all too often treated as disposable in crisis situations and are much more likely to live in poverty and be isolated from our communities. This makes us particularly vulnerable to climate change and less able to access support for our mental health, including the deep feelings of anxiety, fear, anger and grief surrounding the climate crisis many of us experience. This lack of support is often exacerbated if we are multiply marginalised.

Leone, M. L. (2019, Spring). Reframing disability through an ecocritical perspective in Sara Mesa’s Cara de pan.  In E. Fernández & V. L. Ketz (Eds.), Re-imagining Female Disabilities in Luso-Hispanic Women’s Cultural Production [Special Issue]. Journal of Gender and Sexuality Studies / Revista de Estudios de Género y Sexualidades, 45(1), 161-184. DOI: https://www.jstor.org/stable/10.14321/jgendsexustud.45.1.0161.

This article establishes a dialogue between disability studies and ecocriticism to analyze Sara Mesa’s novel Cara de pan (2018), which narrates the relationship between a thirteen-year-old girl bullied at school and a fifty-four-year-old man with an atypical appearance who fixates on limited topics. The analysis examines the hegemony of normativity and dominant social narratives about disability, gender, and sexuality. Grounded in the idea that people with disabilities actively intervene in their environment, the essay argues that the characters’ environmental empathy supports the need for a diversity of experiences and perspectives, positively resituating disability and autism.

Leong, G. (2020). The impacts of climate change on persons with disabilities: An interdisciplinary approach to disability, climate change and policy studies. Pacific Rim International Conference on Disability and Diversity Conference Proceedings. Honolulu, Hawai’i: Center on Disability Studies, University of Hawai’i at Mānoa.

The overall intent of this study is to address the impacts and expected impacts of climate change and disasters on persons with disabilities (PWD), while exploring international policies for resilience initiatives. As a portion of the overall study, this paper was motivated by the recent United Nations Human Rights Council (UN-HRC) (2019) resolution adoption on climate change and the rights of persons with disabilities, which urges governments to adopt a disability-inclusive approach when dealing with climate change strategies. The objective of this paper is to explore academia & research’s role in adaptive capacity approaches to adopting the UN-HRC resolution through a multidisciplinary intersection of disability, climate change and policy studies. The objective is supported by empirical research, theoretical models, and inclusive strategies aimed to improve the safety and quality of life for PWD. This paper’s scope is covered through the development of a resilience framework that includes vulnerability index: exposure, sensitivity, and adaptive capacity (Intergovernmental Panel on Climate Change [IPCC], 2008); and three sets of engagement: theory, application, and praxis (Cho, Crenshaw, & McCall, 2013). Ultimately, the paper’s proposed framework will present an evidence-based, disability-inclusive resilience approach to addressing climate change aimed to influence public perception and policy decision-making. This paper is a tool for disability, climate change, and policy studies academics/researchers, and government officials interested in academia & research’s contribution to resilience planning.

Lindsay, S., Hsu, S., Ragunathn, S., & Lindsay, J. (2022). The impact of climate change related extreme weather events on people with pre-existing disabilities and chronic conditions: a scoping review. Disability and Rehabilitation. DOI: https://doi.org/10.1080/09638288.2022.2150328.

Purpose: People with disabilities experience a disproportionate impact of extreme weather events and there is a critical need to better understand the impact that climate change has for them. Most previous reviews focus on the risk of acquiring a new disability or injury after a climate-related event and not the impact on people with pre-existing disabilities or chronic conditions, which is the purpose of this study.

Methods: We conducted a scoping review while searching seven international databases that identified 45 studies meeting our inclusion criteria.

Results: The studies included in our review involved 2 337 199 participants with pre-existing disabilities and chronic conditions across 13 countries over a 20-year period. The findings demonstrated the following trends: (1) the impact on physical and mental health; (2) the impact on education and work; (3) barriers to accessing health and community services (i.e., lack of access to services, lack of knowledge about people with disabilities, communication challenges, lack of adequate housing); and (4) coping strategies (i.e., social supports and connecting to resources) and resilience.

Conclusions: Our findings highlight the critical need for rehabilitation clinicians and other service providers to explore opportunities to support their clients in preparing for climate-related emergencies.

Linett, M. V. (2020). Literary bioethics: Animality, disability, and the human [Crip Series]. New York: NYU Press.

Uses literature to understand and remake our ethics regarding nonhuman animals, old human beings, disabled human beings, and cloned posthumans.

Lundbad, M. (Ed.). (2020, Autumn). Animality/Posthumanism/Disability [Special Issue]. New Literary History, 51(4). DOI:  https://doi.org/10.1353/nlh.2020.0040.

“The title and focus of this special issue is meant to foreground the potential and pitfalls of thinking through critiques of ‘the human’ in relation to animality and disability within the framework of posthumanism, broadly conceived” (p. v).

Articles in this special issue include:

  • Animality/ Posthumanism/ Disability: An Introduction
  • Being Human, Being Animal: Species Membership in Extraordinary Times
  • Companion Thinking: A Response
  • The Art of Interspecies Care
  • Beyond Caring: Human-Animal Interdependency: A Response
  • We Have Laws for That: A Response to Jack Halberstam
  • Abnormal Animals
  • Restriction, Norm, Umwelt: A Response
  • Disanimality: Disability Studies and Animal Advocacy
  • The Political Economy of Disanimality: A Response
  • On the Transhumanist Imaginary and the Biopolitics of Contingent Embodiment
  • “Where Are You Taking Us?”: A Response
  • The Biopolitical Drama of Joseph Beuys
  • Animal Death as National Debility: Climate, Agriculture, and Syrian War Narrative
  • Atmospherics of War: A Response

Lundblad, M., & Grue, J. (2021). Companion prosthetics: Avatars of animality and disability. In S. McHugh, R. McKay, & J. Miller (Eds.), The Palgrave Handbook of Animals and Literature (pp. 557-574). New York: Palgrave Macmillan.

Avatar is rife with prosthetic relationships that blur the lines between human and animal, human and machine, and even animate and inanimate objects, raising the possibility of more productive conversations about the interface between disability and animality. Our argument in this chapter is that the problematic aspects of the film are not only inter-related, but also productive for developing what we will call companion prosthetics. We develop this concept from origins in disability studies, animality studies, and human-animal studies, illustrating the fertile new ground that exists when these fields meet” (p. 2).

Lupinacci, J., Happel-Parkins, A., & Lupinacci, M. W. (2018). Ecocritical contestations with neoliberalism: Teaching to (un)learn “normalcy.” In S. Gaches (Ed.), Preparing Teachers to Confront Neoliberal Discourses and to Teach Children Equitably [Special Issue]. Policy Futures in Education, 16(6), 652–668. DOI: https://doi.org/10.1177%2F1478210318760465.

This article seeks to address often overlooked cultural assumptions embedded within neoliberalism; specifically, the researchers explore what ecofeminist Val Plumwood describes as centric thinking, leading to a logic of domination. The authors argue that social justice educators and activists who are committed to critiquing neoliberalism must take into consideration the ways in which a logic of domination undergirds the unjust and destructive social and economic ideologies and policies that constitute neoliberalism. The authors examine and share pedagogical moments from experiences in teacher education seeking to: (a) challenge and disrupt dualistic thinking; (b) interrupt perceptions of hegemonic normalcy—referring to a socio-cultural process by which actions, behaviors, and diverse ways of interpreting the world are perceived by dominant society as ‘fitting in’ and being socially acceptable; and, (c) contest false notions of independence—the degree to which an individual is perceived as able to meet their social and economic responsibilities on their own—as measures of success in schools and society. The authors detail how they work with(in) teacher education programs to introduce how an ecocritical approach, drawing from ecofeminist frameworks, identifies and examines the impacts of neoliberal policies and practices dominated by ‘free’ market ideology. The authors assert that educators, especially teacher educators, can challenge harmful discourses that support the problematic neoliberal understandings about independence that inform Western cultural norms and assumptions. Concluding, the authors share a conceptualization for (un)learning the exploitation inextricable from the policies and practices of neoliberalism.

Martínez Benedí, P. (2020, Fall/Winter). A Different Side of the Story: On Neurodiversity and Trees. Iperstoria No. 16, 259-277.

This essay analyzes Richard Powers’s The Overstory (2018), a novel that ostensibly demands an eco-critical reading, under the lens of neurodiversity. Focusing on the idiosyncrasies of sensory perception in autism, the essay explores the atypical engagement with the more-than-human that neurodiversity (and specifically autism) fosters—a kind of engagement that deeply destabilizes neuro-normative, human-centered subjectivity, opening up to more egalitarian ways of relation with the environment. In a novel populated by neurodivergent characters with a keen ecological sensibility, Powers comes close to imagining this kind of non-hierarchical connection with the natural world. The essay explores how neurodiversity works in the novel at a characterological, thematic, and structural level, functioning as a bridge between human and non-human scales. In this way, neurodiversity finely glosses and articulates the kind of animistic, environmental message that Powers instils in his Pulitzer prize winning novel.

Mathers, A. R. (2008, August). Hidden voices: The participation of people with learning disabilities in the experience of public open space. In R. Imrie & H. Thomas (Eds.), The Environment and Disability: Making the Connections [Special Issue]. Local Environment, 13(6), 515-529. DOI: https://doi.org/10.1080/13549830802259912.

The self-advocacy of people with learning disabilities (PWLD) is an issue of high current importance. In the UK 210,000 people have severe and profound learning disabilities, whilst 25 in every 1000 of the population in England has a mild to moderate learning disability (Department of Health, Valuing people: a new strategy for learning disability for the 21st century, London, Stationery Office, 2001). At the most restricted end of the communication spectrum, PWLD are often forgotten members of their communities, whose label “learning disabled” wrongly causes confusion and fear. The Disability Discrimination Act (DDA) 1995 ensured “reasonable” adjustments must be made to environments and buildings so they are accessible to all. However, DDA legislation remains a predominately physical access issue with great attention focused on the built environment and little attention given to the experience of place or external environments. Researchers argue that it is attitudes and interactions in the person–environment relationship that have allowed our “disablist” society to label and segregate members of its community as “disabled”. The research comprised a longitudinal study working with PWLD participants at two sites in Yorkshire and in the northeast of England. This paper examines the resulting visual communication toolkit, able to unlock the experience of public open spaces by PWLD and, when used in context, to aid greater social participation.

Mihail, A. (2022, March 14). The intersections of disability in the face of disaster and climate activism. The Kingfisher Magazine. 

“Past and present catastrophes, such as Hurricane Katrina and the current COVID-19 pandemic, have shown how disabled people are often forgotten by society. The threat of climate change, flooding, heatwaves, droughts and wildfires will undoubtedly heighten their state of vulnerability. What will it take for society to value disabled lives?

According to the social model of disability, mental or physical impairments are not necessarily disabling by themselves. In most cases, they are turned into disabilities due to a society that fails to account for differences from the normative

We live in a deeply inaccessible society, where many are cut off from jobs, town halls, art galleries, educational institutions, restaurants, cinemas and other physical locations needed for personal development, socialisation and entertainment. This is because their bodies and mind, outside of their control, do not conform to how society thinks a human should function. Therefore, it is of little surprise when climate change threatens them disproportionately.”

Mitchell, D. T., Antebi, S., & Snyder, S. L. (Eds.). The Matter of Disability:  Materiality, Biopolitics, Crip Affect [Corporealities: Discourses of Disability Series]. Ann Arbor, MI: University of Michigan Press. DOI: https://doi.org/10.3998/mpub.9365129.

The Matter of Disability returns disability to its proper place as an ongoing historical process of corporeal, cognitive, and sensory mutation operating in a world of dynamic, even cataclysmic, change. The book’s contributors offer new theorizations of human and nonhuman embodiments and their complex evolutions in our global present, in essays that explore how disability might be imagined as participant in the ‘complex elaboration of difference,’ rather than something gone awry in an otherwise stable process. This alternative approach to materiality sheds new light on the capacities that exist within the depictions of disability that the book examines, including Spider-Man, Of Mice and Men, and Bloodchild.

Nocella, A. J., Bentley, J. K. C., & Duncan, J. M. (Eds.). (2012). Earth, animal, and disability liberation: The rise of the eco-ability movement. New York: Peter Lang.

This provocative and groundbreaking book is the first of its kind to propose the concept of Eco-ability: the intersectionality of the ecological world, persons with disabilities, and nonhuman animals. Rooted in disability studies and rights, environmentalism, and animal advocacy, this book calls for a social justice theory and movement that dismantles constructed «normalcy», ableism, speciesism, and ecological destruction while promoting mutual interdependence, collaboration, respect for difference, and inclusivity of our world. Eco-ability provides a positive, liberating, and empowering philosophy for educators and activists alike.

Nocella, A. J., & George, A. E. (in press). Vegans on speciesism and ableism: Ecoability voices for disability and animal justice [Radical Animal Studies and Total Liberation].  New York: Peter Lang Publishing, Inc. DOI: https://doi.org/10.3726/b18574.

This powerful intersectional social justice book examines animal, disability, and environmental oppression and justice. Located in disability studies, sociology, environmental justice, food justice, and critical animal studies, this book engages the reader in an intersectional ecological manner for an inclusive interdependent global community. This outstanding collection of original articles by scholars from around the world discusses the need to acknowledge the relationships among nonhuman animals, those with disabilities, and the environment. Adaptive sports from mountain biking to rock climbing is saving the lives of those with disabilities from extreme depression and suicide at the same time those with disabilities are becoming some of the most loyal advocates for defending the environment from human destruction. Those with disabilities are being welcomed into the animal rights movement and also introduced to nonhuman animals not as merely service animals, but as friends, allies, and companions.

Nocella, A. J., George, A. E., & Lupinacci, J. (Eds.). (2019). Animals, disability, and the end of capitalism: Voices from the eco-ability movement [Radical Animal Studies and Total Liberation Series]. New York: Peter Lang Publishing, Inc. DOI: https://doi.org/10.3726/b14134.

Animals, Disability, and the End of Capitalism is a collection of essays from the leaders in the field of eco-ability. The book is rooted in critical pedagogy, inclusive education, and environmental education. The efforts of diverse disability activists work to weave together the complex diversity and vastly overlooked interconnections among nature, ability, and animals. Eco-ability challenges social constructions, binaries, domination, and normalcy. Contributors challenge the concepts of disability, animal, and nature in relation to human and man. Eco-ability stresses the interdependent relationship among everything and how the effect of one action such as the extinction of a species in Africa can affect the ecosystem in Northern California. Animals, Disability, and the End of Capitalism is timely and offers important critical insight from within the growing movement and the current academic climate for such scholarship. The book also provides insights and examples of radical experiences, pedagogical projects, and perspectives shaped by critical animal studies, critical environmental studies, and critical disability studies.

Nocella, A. J., George, A. E., & Schatz, J. L. (2017). The intersectionality of critical animal, disability, and environmental studies: Toward eco-ability, justice, and liberation [Critical Animal Studies and Theory]. Lanham, MD: Lexington Books.

The Intersectionality of Critical Animal, Disability, and Environmental Studies: Toward Eco-ability, Justice, and Liberation is an interdisciplinary collection of theoretical writings on the intersectional liberation of nonhuman animals, the environment, and those with disabilities. As animal consumption raises health concerns and global warming causes massive environmental destruction, this book interweaves these issues and more. This important cutting-edge book lends to the rapidly growing movement of eco-ability, a scholarly field and activist movement influenced by environmental studies, disability studies, and critical animal studies, similar to other intersectional fields and movements such as eco-feminism, environmental justice, food justice, and decolonization. Contributors to this book are in the fields of education, philosophy, sociology, criminology, rhetoric, theology, anthropology, and English.

Nygren, A. (2023). Empathy with nature and an autistic spirituality. In A. Dare & V. Fletcher (Eds.), Labors of Love and Loss. Radical Acts of Human, Plant, and Nonhuman Mothering [Special Issue]. Journal of Ecohumanism, 2(1), 93–108. DOI: https://doi.org/10.33182/joe.v2i1.2740.

Anna Stenning does in the anthology Neurodiversity. A New Critical Paradigm (2020) introduce an autistic ethics using the autobiographies of Greta Thunberg (No One Is Too Small to Make a Difference (2019)) and Temple Grandin (Animals in Translation (2005)). Stenning points to how this autistic ethics do expand its acts of care to the more-than-human. Grandin describes her being in the world as more attuned to animals than humans. Thunberg argues that her Asperger’s is the reason why she can care so totally for the climate. This article further investigates the intersection of autism and the more-than-human, or the post humanist. Using the works of openly autistic authors Madeleine Ryan (A Room Called Earth (2020)) and Hannah Emerson (You Are Helping This Great Universe Explode (2020)) as well as Emily Dickinson, posthumously diagnosed with autism. I investigate the autistic theme of nature and the autistic relationship to other species. This relation often seems to be stronger and more genuine than the relation to other humans. I propose that the autistic sense of the more-than-human is at once a response to the oppressive view of the autistic as less-than-human – a way of finding one’s allies outside the realms of human civilization – and a special kind of autistic worldly spiritualness that includes an ethics that do not segregate one life form from another.

Office of the United Nations High Commissioner for Human Rights. (2020, April). Analytical study on the promotion and protection of the rights of persons with disabilities in the context of climate change. New York: United Nations General Assembly.

The present analytical study is submitted pursuant to Human Rights Council resolution 41/21. In the report, the impacts of climate change on persons with disabilities are examined; human rights obligations and the responsibilities of States and other actors
in relation to disability-inclusive approaches identified; and good practices shared. The
report ends with conclusions and recommendations.

Office of the High Commissioner for Human Rights. (n.d.). Issues in focus: The impact of climate change on the rights of persons with disabilities: OHCHR and climate change [Website]. New York: United Nations General Assembly.

Reports OHCHR’s work on disability-inclusive climate action, including activities, events, and reports.

Ortiz, N. (2022, February). Crip ecologies: Complicate the conversation to reclaim power. Poetry Magazine. Chicago: Poetry Foundation.

“Crip ecologies describe the messy, diverse, and profoundly beautiful ecosystems which exist for disabled people. It is impossible to fit ourselves to a mold that nondisabled people adhere to, which allows capitalism (making money and paying money to live) to flourish, borders to be maintained, and uniform solutions to address some of our most pressing and urgent problems like climate change.”

Perry, K. (2023). Climate migration and the rights of persons with disabilities. In T. Walker, J. McGaughey, G. Machnik-Kekesi, & V. Kelly (Eds.), Environmental migration in the face of emerging risks (pp.121–135). Palgrave Macmillan, Cham. DOI: https://doi.org/10.1007/978-3-031-29529-4_7.

This chapter explores the experiences of persons with disabilities when migrating due to climate change and other environmental factors and offers recommendations on how to protect, respect, and fulfill their human rights. The chapter uses the human rights model of disability when analyzing the literature and offering recommendations. Following the introduction to key topics and models, the chapter surveys selected international instruments, including treaties, conventions, outcome documents, etc., to examine how the rights of persons with disabilities are addressed in climate emergencies and in the migration literature. The chapter next highlights best practices from climate disasters and emergencies that can be used in the context of migrations due to climate change and other environmental factors. The chapter concludes by offering recommendations on how to advance the human rights of persons with disabilities in climate-related migration.

Preece, B. (2018). Environments, ecologies and climates of crises: Engaging disAbility arts and cultures as creative wilderness. In B. Hadley & D. McDonald (Eds.), The Routledge Handbook of Disability Arts, Culture and Media Studies (pp. 281-294). New York: Routledge.

This chapter provides the premise that Western orientations towards our perceptions of the ‘environment,’ ‘ecology,’ ‘nature,’ and ‘wilderness’ are synonymous with many of our societal perceptions of disability. Though tension between current discourses of disability cultures and environmental restoration remains, people with disabilities are actively positioned to advocate on behalf of variance, deviance, and mutability. There is a tendency for non-disabled environmental justice advocates to highlight the disabling impacts of resource extraction or contamination in ways that treat the tragedy of disabled bodies as self-evident. The social interpretation of disability advocates through disability studies for an embracing of the disabled person into the social/built environment as a recognised necessary phenomenon on a continuum. The effects of the climate crisis have quite possibly forced the need for an exaggerated form of performance – an acceleration of the improvisatory – unto the more-than-human world: inextricably a co-performative paradigm.

Puar, J. K. (2017). The right to maim: Debility, capacity, disability [ANIMA: Critical Race Studies Otherwise Series]. Durham, NC: Duke University Press. DOI: https://doi.org/10.1215/9780822372530.

In The Right to Maim Jasbir K. Puar brings her pathbreaking work on the liberal state, sexuality, and biopolitics to bear on our understanding of disability. Drawing on a stunning array of theoretical and methodological frameworks, Puar uses the concept of “debility”—bodily injury and social exclusion brought on by economic and political factors—to disrupt the category of disability. She shows how debility, disability, and capacity together constitute an assemblage that states use to control populations. Puar’s analysis culminates in an interrogation of Israel’s policies toward Palestine, in which she outlines how Israel brings Palestinians into biopolitical being by designating them available for injury. Supplementing its right to kill with what Puar calls the right to maim, the Israeli state relies on liberal frameworks of disability to obscure and enable the mass debilitation of Palestinian bodies. Tracing disability’s interaction with debility and capacity, Puar offers a brilliant rethinking of Foucauldian biopolitics while showing how disability functions at the intersection of imperialism and racialized capital.

Purcell, S. (2019). Beckett and disability biopolitics: The case of Cuchulain. In S. Kennedy (Ed.), Samuel Beckett and Biopolitics [Special Issue].  Estudios Irlandeses, 14(2), 52-64. DOI: https://doi.org/10.24162/EI2019-9171.

In his depiction of the hero Cuchulain, Samuel Beckett interrogates how disability and compulsory able-bodiedness are foundational myths for the Irish Free State. Taking the interpolation of disability in biopolitics, this essay examines the normalising impulses in revivalist literature and criticism, exemplified by Lady Gregory, Standish O’Grady, WB Yeats and Daniel Corkery. Against this normalising, nationalising literature, I situate Beckett’s satirical renderings of Cuchulain in ‘Censorship and the Saorstat’ and Murphy, as evidence of a profound discomfort and frustration with the biopolitical mechanisms of governance in the newly-founded Irish State.

Ray, S. J. (2013, Spring). Normalcy, knowledge, and nature in Mark Haddon’s The Curious Incident of the Dog in the Night-Time. Disability Studies Quarterly, 33(3). DOI: http://dx.doi.org/10.18061/dsq.v33i3.3233.

This article analyzes Mark Haddon’s 2003 novel, The Curious Incident of the Dog in the Night-Time, using a combination of both disability studies theory and ecocriticism.  The author argues that the novel’s main character, Christopher Boone, presents a social model of disability by challenging dominant society’s treatment of him as ‘not normal.’ Christopher is ostensibly diagnosed with Asperger’s Syndrome, although the novel never explicitly labels him as disabled in any way. Through Christopher’s views of nature, language, knowledge, and social constructions of disability, we learn that disability is an unstable category, and that dominant society can be disabling.  Importantly, though, Christopher’s critique of society is, as the author argues, fundamentally environmental. That is, Christopher’s views of language, knowledge, and even the more-than-human world itself are central to his destabilization of the category of disability. Christopher’s environmental sensibility and critique of society’s disabling qualities emerge primarily through his discussions of language, which he finds suspect because it distances humans from the world it describes.  Thus, the novel suggests that the disabling features of society that Christopher encounters are the same features that distance humans from nature, particularly through language.

Ray, S. J. (2009, August). Risking bodies in the wild: The “corporeal unconscious” of American adventure culture. In D. Mincyte, M. J. Casper, & C.L. Cole (Eds.), Sports and Environmental Politics II [Special Issue]. Journal of Sport & Social Issues, 33(3), 257-284. DOI: https://doi.org/10.1177%2F0193723509338863.

At the heart of American adventure sports is the appeal of personal challenge that has roots in 19th-century “wilderness cults. Preserving wilderness and testing oneself against it were part of a search for moral, physical, and even national purity. But, as critics have begun to argue, racism, expansion, and exclusion underpin the wilderness movement. Although these exclusions have been identified, there has been less attention to these exclusions in contemporary adventure culture and environmental thought, which borrow values from the early wilderness movement and suggest that an environ-mental ethic arises from risking the body in the wild. By examining adventure culture through disability studies, this article exposes the relationship between environmentalism and ableism. It argues that disability is the category of “otherness” against which both environmentalism and adventure have been shaped and revises environmental thought to include all kinds of bodies.

Ray, S. J., & Sibara, J. (Eds.). (2017). Disability Studies and the environmental humanities: Toward an eco-crip theory.  Lincoln & London: University of Nebraska Press.

Although scholars in the environmental humanities have been exploring the dichotomy between ‘wild’ and ‘built’ environments for several years, few have focused on the field of disability studies, a discipline that enlists the contingency between environments and bodies as a foundation of its scholarship. On the other hand, scholars in disability studies have demonstrated the ways in which the built environment privileges some bodies and minds over others, yet they have rarely examined the ways in which toxic environments engender chronic illness and disability or how environmental illnesses disrupt dominant paradigms for scrutinizing ‘disability.’ Designed as a reader for undergraduate and graduate courses, Disability Studies and the Environmental Humanities employs interdisciplinary perspectives to examine such issues as slow violence, imperialism, race, toxicity, eco-sickness, the body in environmental justice, ableism, and other topics. With a historical scope spanning the seventeenth century to the present, this collection not only presents the foundational documents informing this intersection of fields but also showcases the most current work, making it an indispensable reference.

Salvatore, C.,  & Wolbring, G. (2021). Children and Youth Environmental Action: The Case of Children and Youth with Disabilities. In C. Davey & M. Tataryn (Eds.), Studies and Sustainable Ecology [Special issue]. Sustainability, 13(17), 9950. DOI: https://doi.org/10.3390/su13179950.

Youth environmental activism is on the rise. Children and youth with disabilities are disproportionally impacted by environmental problems and environmental activism. They also face barriers towards participating in activism, many of which might also apply to their participation in environmental activism. Using a scoping review approach, we investigated the engagement with children and youth with disabilities by (a) academic literature covering youth environmental activism and their groups and (b) youth environmental activism group (Fridays For Future) tweets. We downloaded 5536 abstracts from the 70 databases of EBSCO-HOST and Scopus and 340 Fridays For Future tweets and analyzed the data using directed qualitative content analysis. Of the 5536 abstracts, none covered children and youth with disabilities as environmental activists, the impact of environmental activism or environmental problems such as climate change on children and youth with disabilities. Fourteen indicated that environmental factors ‘caused’ the ‘impairments’ in children and youth with disabilities. One suggested that nature could be beneficial to children and youth with disabilities. The tweets did not mention children and youth with disabilities. Our findings suggest the need for more engagement with children and youth with disabilities in relation to youth environmental activism and environmental challenges.

Sánchez Barba, M. G. (2020). “Keeping them down”: Neurotoxic pesticides, race, and disabling biopolitics. In R. Lee (Ed.), Special Section on Chemical Entanglements: Gender and Exposure. Catalyst: Feminism, Theory, Technoscience, 6(1), 1-31. DOI: https://doi.org/10.28968/cftt.v6i1.32253.

Chlorpyrifos, the most widely used insecticide in the US, has gained great notoriety as a contested chemical substance after the U.S. Environmental Protection Agency refused to ban it in 2017. Arguing that scientific studies support their observations and suspicions that agricultural pesticides subtly produce neurological and cognitive harm, concerned groups continue to demand US regulatory agencies to ban this chemical. Their narratives demonstrate how the maintenance of unequal racial and capitalist orders across generational time is tied to small chemical exposures permitted by state regulatory agencies during critical temporalities in the life course. This essay shows the importance of including local perspectives in research that seeks to understand how concerns for the mass neurological and cognitive disabling emerge from lived experiences entangled in histories of racism, exploitation, and neglect. Interweaving feminist science and technology studies, queer theory, and critical disability studies, this analysis contributes to the limited scholarship on cognitive disabling in contexts of environmental injustice through exposure to industrially produced chemicals.

Santinele Martino, A., & Lindsay, S. M. (2020). The Intersections of Critical Disability Studies and Critical Animal Studies [Special Issue]. Canadian Journal of Disability Studies, 9(2). DOI: https://doi.org/10.15353/cjds.v9i2.

“The papers in this special issue build on an exciting, and fast growing, body of scholarship located at the intersection of critical disability studies and critical animal studies, shedding light on disablism and speciesism as interconnecting oppressions, how animality and disability are mutually constitutive, as well as the tensions and coalitions shared by these two related fields” (p. 1).

Articles in this special issue include

  • Normative Tensions in the Popular Representation of Children with Disabilities and Animal-Assisted Therapy
  • Rights and Representation: Media Narratives about Disabled People and Their Service Animals in Canadian Print News
  • At Both Ends of the Leash: Preventing Service-Dog Oppression Through the Practice of Dyadic-Belonging
  • Interspecies Blendings and Resurrections: Material Histories of Disability and Race in Taxidermy Art
  • ‘What on earth was he—man or animal?’: Posthuman Permeability in H.G. Wells’s The Island of Doctor Moreau
  • Tricky Ticks and Vegan Quips: The Lone Star Tick and Logics of Debility

Saxton, M., & Ghenis, A. (2018). Disability Inclusion in Climate Change: Impacts and Intersections. In Climate Change and Intersectionality [Special Issue]. Interdisciplinary Perspectives on Equality and Diversity, 4(1).

The community of people with disabilities is uniquely affected by devastation brought on by climate change. This population is increasingly appearing on lists of “vulnerable” among many other groups in the social justice framework. Public policy in several countries, the Red Cross and United Nation’s documents have begun to include the voices of persons with disabilities among the planning constituencies. Yet the needs of this constituency are poorly understood regarding which measures could realistically enable survival in environmentally compromised circumstance. This very diverse group comprises approximately 10 to 15% of the global population, and within all other sub-populations, this figure will likely increase with climate change impact. Discriminatory attitudes and policies tend to simplify this multiply intersectional population to “people with special needs.” This simplification ignores the diverse, complex needs and circumstances of individuals with disabilities, for those with visual, hearing, and mobility impairments, and so on, as well as their various socio-economic cross-constituencies such as gender, ethnicity, age, etc. In this context, focus on climate change and disability is disturbingly rare. This article by U.S.-based authors explores key intersectional issues emphasizing their research in the U.S. related to disability and climate change impact, and recommending an educational, research and advocacy agenda for both the Climate Change and the Disability Rights movements.

Schaffer, D. (2023, March). Disabilities in disaster situations: How a rescuer handles what they encounter. In K. Takahashi, H. J. Park, & T. Conway (Eds.), 37th Annual Pacific Rim International Conference on Disability & Diversity 2022: Conference Proceedings [Feature Issue]. Review of Disability Studies, 18(3).

Individuals with disabilities are often disproportionately affected by disaster. With little research focused on rescue operations impacting individuals with disabilities during large disasters, three themes are reviewed: re-leveling expectations; misunderstanding of triage and crisis medical protocols; and light switch fallacy by responders and individuals with disabilities before, during, and after rescue operations.

Schleck, G., & Ben-Alon, L. (2024). Eco-ableism and access circularity in natural building. Frontiers of Architectural Research. DOI: https://doi.org/10.1016/j.foar.2023.11.005.

The climate crisis disproportionately impacts disabled people. Yet climate-related advocacy, planning, and policymaking often neglect to thoughtfully include disabled people. Responding to this gap, disabled and neurodivergent environmental activists coined the term eco-ableism to describe discrimination and silencing toward disabled and neurodivergent people (i.e., ableism) arising in environmental spaces (i.e., eco-ableism). Relatedly, building operations and construction practices contribute a significant percentage of global, energy-related CO2 emissions annually, which calls into question the relationships between the impending climate crisis, disability justice, and architecture. Climate-specific, natural building materials and methods present a potential pathway toward a more sustainable built future: low-carbon, locally sourced, minimally processed, and nontoxic materials. Despite a critical overlap, there is little published research on material access in the production phase and human access in the occupation phase of natural buildings. Applying eco-ableism and material circularity in an architectural framework, this research aims to investigate the gaps and possibilities of access, natural material applications, and resulting US natural buildings informed by scholarship in critical disability studies and semi-structured interviews with natural building professionals.

Schmidt, J. (2022). Cripping environmental education: Rethinking disability, nature, and interdependent futures. Australian Journal of Environmental Education First View. DOI: https://doi.org/10.1017/aee.2022.26.

“In this article, I call for a cripping of environmental education as a necessary move in shifting away from the field’s current conceptions of disability as defect and deficiency, and towards disrupting the structures and processes that operate as normalizing technologies within ableism/sanism. Through an examination of the ways that the field of environmental education has/has not engaged critical disability politics, I illuminate how disability is not often included within environmental education literature. When it is, it is often through the use of disability as metaphor or through recommendations for best practices in accommodating disabilities. More often though within environmental education, disability has operated as a hidden curriculum, underpinning much of the field’s curricular, pedagogical, and even philosophical foundations. Through a cripping of the field these compulsory able-bodied/able-minded assumptions are made apparent. I suggest that by centering crip bodies and minds through cripistemologies, we might enable new ways of knowing, being in, connecting to, and understanding the natural world.”

Schweik, S. (2017). Agent orange, monsters, and we humans. In H. Davis Taïeb (Ed.), From the Monstrous to the Human [Special Issue]. ALTER, European Journal of Disability Research, 11, 65-77. DOI: https://doi.org/10.1016/j.alter.2016.12.005.

This paper recounts the work of the American artist collective Yelling Clinic, a group of artists who have direct experience of disability and war, in collaboration with Vietnamese disabled artists and activists in Vietnam in 2011. Focusing on the toxic ecological effects of the herbicide Agent Orange, the essay explores the ethics of Agent Orange representation, focusing on a series of art pieces (and the collaborations that produced them) that work not as documentary evidence of the ravages of dioxin, not as an archive of monstrosity, but as vibrant expressions of and within a complex nexus of disability arts cultures.

Seetharaman, K., Mahmood, A., Rikhtehgaran, F., Akbarnejad, G., Chishtie, F., Prescott, M., Chung, A. Mortenson, W. B. (2024) Influence of the built environment on community mobility of people living with visual disabilities: A scoping review. Urban, Planning and Transport Research, 12(1), Article: 2296891. DOI: https//doi.org/10.1080/21650020.2023.2296891.

Understanding how the outdoor environment shapes the community mobility of people with visual disabilities is key to designing an accessible public realm and facilitating their rights to use outdoor spaces. A scoping review was conducted to explore 1) What aspects of the built environment affect the community mobility of persons with visual disabilities? and 2) How does the built environment affect the community mobility of persons with visual disabilities? Forty-three peer-reviewed publications from 2000 to 2022 were included after conducting database searches, screening of articles, and data charting. Studies focused on micro-environmental features related to sidewalks and crosswalks (e.g. landmarks, curbs, curb ramps, tactile warning/guiding surfaces, and accessible pedestrian signals), and broad environmental factors (e.g. neighbourhood amenities and street layout) and their influence on orientation, wayfinding, and safety. The paper discusses the role of the built environment in 1) posing barriers to outdoor mobility (e.g. potholes, poorly designed curb cuts, obstacles at waist-height or eye-level, poor lighting, inadequate pedestrian signal, complicated street layout), and 2) offering cues (e.g. visual, tactile, auditory, olfactory, kinaesthetic) for spatial perception and navigation. Focusing on how the built environment shapes community mobility is necessary to enhance accessibility through urban planning and design and assistive technology.

Selanon, P., & Chuangchai, W. (2023). Improving accessibility to urban greenspaces for people with disabilities: A modified universal design approach. Journal of Planning Literature. DOI: https://doi.org/10.1177/08854122231212662.

Despite the integration of universal design, access to urban greenspaces, which provide multiple health benefits, has been restricted among people with disabilities, particularly in developing countries. This article argues that the sole use of the seven principles of universal design is inadequate for urban greenspace planning as it consistently fails to prevent serious injuries, accommodate multiculturalism, and disregard subjective feelings when addressing people with disabilities. Additional approaches, including a safety strategy, diverse cultural behavior acceptability, and emotional design through landscape naturalness, are considered to improve accessibility, thereby reducing urban health inequalities and achieving an inclusive city.

Shotwell, A. (2016). Against purity: Living ethically in compromised times. Minneapolis: University of Minnesota Press.

In Against Purity, Alexis Shotwell proposes a powerful new conception of social movements as custodians for the past and incubators for liberated futures. Against Purity undertakes an analysis that draws on theories of race, disability, gender, and animal ethics as a foundation for an innovative approach to the politics and ethics of responding to systemic problems.

Slopek, C. (2021). Aboriginal speculations: Queer rhetoric, disability, and interspecies conviviality in The Interrogation of Ashala Wolf. In B. Burger, D. Kern, & L. Mattila (Eds.), Gender and Sexuality in Australian Speculative [Special Issue]. gender forum Issue 81.

The Anthropocene looms large in the 21st century, and queer and disabled people continue to be exposed to harassment and discrimination. What do these issues have in common, though? In Ambelin Kwaymullina’s speculative fiction novel The Interrogation of Ashala Wolf (2012), queer discourse collaborates with, promotes, and diversifies a non-anthropocentric world order, simultaneously implicating a dis-/ability dialectic. This article brings together queer, disability, interspecies studies and literary analysis to explore how Kwaymullina’s young adult novel creates links between queerness and interspecies relations and how disability comes into play. The rhetoric used against children with so-called special abilities in the novel, who come to occupy the structural position of the queer in Kwaymullina’s narrative at the expense of those living with disabilities, as well as the role interspecies conviviality plays for future community construction are focal points of the article. For the latter part, in particular, this article draws on Aboriginal knowledge systems to explore how The Interrogation of Ashala Wolf weaves these marginalised epistemologies into literature and thus changes the field of speculative fiction.

Smith, A. F. (2021). Surviving sustainability: Degrowth, environmental justice, and support for the chronically ill. The Journal of Philosophy of Disability, 1, 175-199. DOI: https://doi.org/10.5840/jpd20217263.

The quest for ecological sustainability—specifically via prioritizing degrowth—creates significant, often overlooked challenges for the chronically ill. I focus on type-1 diabetes, treatment for which depends on nonrenewables and materials implicated in the global proliferation of toxins that harm biospheric functions. Some commentators suggest obliquely that seeking to develop ecologically sustainable treatments for type-1 shouldn’t be prioritized. Other medical concerns take precedence in a post-carbon world marked by climate change and widespread ecological devastation. I challenge this view on three grounds. Its proponents (i) fail to treat type-1 as the public health issue it is, particularly within the context of what Sunaura Taylor calls disabled ecologies. They (ii) deny persons with type-1 an equal opportunity to pursue survival. And they (iii) presume without warrant that treating type-1 is an all-or-nothing affair. Indeed, research by biohackers points to suboptimal but potentially workable ways to make type-1 survivable in a post-carbon future—so long, I stress, as their findings are cripped in a manner that foregrounds the demands of environmental justice.

Socha, K. A., Bentley, J. K. C., & Schatz, J. L. (Eds.). (2014, May).  Eco-Ability the Intersection of Earth, Animal, and Disability [Special Issue]. Journal for Critical Animal Studies, 12(2). Retrieved from: http://www.criticalanimalstudies.org/volume12-issue-2-2014/.

“This special issue focuses on eco-ability, which ‘explore[s] the intersection of dis-ability studies, environmental awareness, and nonhuman animal liberation'” (p. 1).

This issue includes the following articles and reviews:

  • An Introduction to Eco-Ability: The Struggle for Justice, with Focus on Humans with Disabilities and Nonhuman Animals
  • An Interview with Sunaura Taylor
  • Grace for a Cure: Poisoned Ethics and Disabled-Nonhuman Images
  • Foreignness and Animal Ethics: A Secular Vision of Human and Constructed Social Disability
  • Applying the Argument from Marginal Cases to the Protection of Animal Subjects in Research: A Blueprint for Studying Nonhuman Animals in a Post-vivisection World
  • Intersectionality and the Nonhuman Disabled Body: Challenging the Neocapitalist Techno-scientific Reproduction of Ableism and Speciesism
  • Animal Crips
  • Ability Privilege: A Needed Addition to Privilege Studies
  • As the World Burns: 50 Simple Things You Can Do to Stay in Denial (2007)
  • Avatar (2009) and District 9 (2009) – Animals, Aliens, and (Dis)abled Bodies: A Post-structural, Comparative Analysis

Spielhagen, A.,Hernández, L. H., & Blevins, M. (2021, October 21). “My dude, are you tired? I’m tired:” An intersectional nethodological intervention. Frontiers in Communication, Sec. Science and Environmental Communication, 6(722465). DOI: https://doi.org/10.3389/fcomm.2021.722465.

This manuscript is a methodological intervention that addresses ethical considerations associated with conducting research in outdoor spaces, particularly with communities of color and other marginalized communities. The core issue is that BIPOC individuals, LGBTQIA + individuals, and disabled individuals face discrimination and violence in outdoor/recreational spaces. By investigating these issues, scholars can intensify the problem. We hope that our perspectives can assist ethical decision-making processes in methodology, advocacy, and interaction with outdoor communities of color.

Stavrianos, A., & Pratt-Adams, S. (2022, June). Representations of the benefits of outdoor education for students with learning disabilities: A thematic analysis of newspapers. Open Journal of Social Sciences, 10(6), 256-268. DOI: https://doi.org/10.4236/jss.2022.106020.

Outdoor Education (OE) has been described as an education taking place in a natural environment where the students learn about their natural surroundings (Torkos, 2017). Outdoor education was one of the precursors of Environmental Education (EE). Outdoor education is a non-formal education and is classified as an educational approach which occurs outside the classroom and with a wide range of subjects such as the natural environment, culture, mathematics, music, physical science. This study adopts a qualitative paradigm in order to explore the integration of Outdoor Education in the philosophy of inclusion. Eight newspaper articles representing stances and opinions of stakeholders in education, were thematically analysed into explore popular representations of benefits of outdoor education for students with learning difficulties. The themes which emerged from the data were: an active attitude towards learning, a holistic approach—transferable benefits, Inclusion, Edutainment, and Experiential Learning. The key themes identified, indicate that learners within an outdoor education context seem to be active participants of the learning process. Moreover, outdoor education is expandable to the learners’ environments, while it seems that academically and/or socially less able pupils in particular, can benefit out of outdoor education.

Stein, P. J. S,. & Stein, M. A. (2022, January). Comment: Climate change and the right to health of people with disabilities. The Lancet Global Health, 10(1), e24-e25. DOI: https://doi.org/10.1016/S2214-109X(21)00542-8.

“Climate change exacerbates existing inequalities with indirect disproportionate effects on people with disabilities due to their lack of access to health-care services and increased exposure to social determinants of health such as poverty, and lack of access to education, employment, or adequate housing” (p. e24).

Stein, P.J.S., & Stein, M. A. (2022, February). Disability, human rights, and climate justice. Human Rights Quarterly, 44(1), 81-110. DOI: https://doi.org/10.1353/hrq.2022.0003.

The universally dire threat of climate change disproportionately affects marginalized populations, including the over one billion persons with disabilities worldwide. States that disregard the Paris Agreement, or exclude disabled persons from climate change mitigation and adaptation efforts, are violating agreed-upon human rights obligations. Notably, the rights contained in the UN Convention on the Rights of Persons with Disabilities, are threatened by climate change. To date, however, disability has largely been excluded from international climate change negotiations as well as national-level discharge of climate-related measures. By contrast, a disability human rights approach views disabled persons as disproportionately experiencing environmental threats and unnatural disasters due to their exclusion from state laws, policies, and services available to their non-disabled peers. Additionally, a disability human rights approach mandates the removal of exclusionary barriers and the implementation of positive measures to ensure the equitable treatment of individuals with disabilities. Achieving disability-inclusive climate justice requires “participatory justice”—empowering persons with disabilities to ascertain climate mitigation and adaptation approaches that are efficacious for, successfully implementable by, and accountable to disabled people. Disability-inclusive climate justice solutions are in synergy with universal climate justice goals and benefit entire societies, not “only” those with disabilities.

Stein, P. J. S., Stein, M. A., Groce, N., & Kett, M. 2023). The role of the scientific community in strengthening disability-inclusive climate resilience. Nature Climate Change, 13, 108–109. DOI: https://doi.org/10.1038/s41558-022-01564-6.

Despite the trajectory towards climate catastrophe, governments are failing to take disability-inclusive climate action. We discuss how the scientific community could advance and hasten the development of disability-inclusive climate resilience, and which areas should be prioritized.

Stone, K. (2024). The earth’s prognosis: Doom and transformation in game design. In L. op de Beke, J. Raessens, S. Werning, & G. Farca (Eds.), Ecogames: Playful Perspectives on the Climate Crisis (pp. 447-462). Amsterdam: Amsterdam University Press. DOI:  https://doi.org/10.5117/9789463721196_ch21.

This chapter describes the design of four games created by the author: Ritual of the Moon (2019), Humaning (2017), the earth is a better person than me (2018), and UnearthU (2022). Each of these games portray aspects of physical and emotional transformation, and the way that transformation may come about through varied connections to the environment fostered primarily through gameplay accessing the player’s imagination. The paper puts together disability studies scholarship with ecocriticism to analyze the common affects of the climate crisis, such as despair, anxiety, and doom through the lens of game creation.

Tamopubolon, G. (2023, January). Climate justice for persons with disability: Few harmed much, fewer still harmed too much [WIDER Working Paper 2023/2]. Helsinki: United Nations University World Institute for Development Economics Research (UNU-WIDER). DOI: https://doi.org/10.35188/UNU-WIDER/2023/310-9.

Building on Rawls’ theory of justice and Sen’s theory of capabilities, I present an outline of social justice under climate shocks, illustrating it with the experiences of persons with disability. Social justice holds when inequality is responded to by rules that afford more primary goods, such as rights and incomes, to those who have less—the maximin principle of the Rawlsian social welfare function. Climate injustice consists in putting more climate bads, not primary goods, on those with slender shoulders—a maximin social ill-fare function. Cross-country climate injustice is a larger instance of this. The developed world has achieved much economic progress (including more primary goods) on the back of burning fossil fuels, which has put the planet on a heating curve that puts massive climate bads on lives and livelihoods today and in future. Most of these bads are put on the shoulders of developing countries. This work addresses within-country climate injustice, such as when persons with disability shoulder extra losses in capabilities, especially being without drinking water for 24 hours. The significant capability losses estimated to have been endured by persons with disability in Indonesia in 2018 and 2020 should inform a more enlightened and socially just response to climate injustice so that, along a just transition, few are harmed much, fewer still harmed too much.

Tatano, V., & Revellini, R. (2023). Excluded bodies: The body dimension of disability in the project for environmental accessibility. In P. Franzo & C. Scarpitti (Eds.), Bodies and Care [Special Issue]. OFFICINA: Quarterly Journal of Architecture, Technology and Environment No. 41. DOI: https://doi.org/10.57623/2384-9029.2023.41.52-61.

Barriers in cities and public spaces limit the autonomy of movement and life of people with physical disabilities. In this way, discrimination is more evident and fosters ableism, an ever-expanding approach that tends to favour bodies that can perform and develop as autonomous and self-sufficient entities, while discriminating those that do not correspond to standards arbitrarily set by society.

The paper focuses its attention to the body dimension of disability and its role concerning projects for environmental accessibility, to overcome the dualism between “able” bodies and “dis-abled” bodies and aims at the construction of buildings and spaces for real bodies.

Taylor, S. (2017). Beasts of burden: Animal and disability liberation. New York: The New Press.

How much of what we understand of ourselves as ‘human’ depends on our physical and mental abilities—how we move (or cannot move) in and interact with the world? And how much of our definition of ‘human’ depends on its difference from ‘animal’? Drawing on her own experiences as a disabled person, a disability activist, and an animal advocate, author Sunaura Taylor persuades us to think deeply, and sometimes uncomfortably, about what divides the human from the animal, the disabled from the nondisabled—and what it might mean to break down those divisions, to claim the animal and the vulnerable in ourselves, in a process she calls ‘cripping animal ethics.’ Beasts of Burden suggests that issues of disability and animal justice—which have heretofore primarily been presented in opposition—are in fact deeply entangled. Fusing philosophy, memoir, science, and the radical truths these disciplines can bring—whether about factory farming, disability oppression, or our assumptions of human superiority over animals—Taylor draws attention to new worlds of experience and empathy that can open up important avenues of solidarity across species and ability.

Taylor, S. (2019). Disability and Interdependence. In S. King, R. S. Carey, I. Macquarrie, V. N. Millious & E. M. Power (Eds.), Messy eating: Conversations on animals as food (pp. 143-156). New York: Fordham University Press.

Even as a young child, Sunaura Taylor, now an artist, activist, and disability and animal studies scholar, understood that humans, animals, and the environment are intensely interconnected. Taylor’s ecological orientation is not simply an intellectual focus but rather a set of political beliefs she endeavors to embody in her everyday life, though she admits that doing so is rarely easy. Taylor’s work demands that audiences rethink the worthiness of vulnerability, of dependency, and of interdependency, particularly as these concepts speak to shared experiences among all living organisms in times of environmental turmoil and fragility.

United Nations General Assembly, Human Rights Council. (2020, April). Analytical study on the promotion and protection of the rights of persons with disabilities in the context of climate change: Report of the Office of the United Nations High Commissioner for Human RightsNew York: Author.

“The present analytical study is submitted pursuant to Human Rights Council
resolution 41/21. In the report, the impacts of climate change on persons with disabilities are examined; human rights obligations and the responsibilities of States and other actors in relation to disability-inclusive approaches identified; and good practices shared. The report ends with conclusions and recommendations” (p. 1).

An easy-read version of the report is also available.

Wall-Reinius, S., Kling, K. G., & Ioannides, D. (2022). Access to nature for persons with disabilities: Perspectives and practices of Swedish tourism providers. Tourism Planning & Development Online First. DOI: https://doi.org/10.1080/21568316.2022.2160489.

Despite the growing popularity of outdoor recreation, nature is not equally accessible to everyone. In the case of persons with disabilities, access to nature remains a largely under-researched area, especially in terms of the role of private and public providers of products and facilities for a diverse range of visitors. This study investigates the challenges and opportunities for developing inclusive forms of accessible nature-based tourism in three different natural settings in Sweden. By focusing on the supply side of nature-based tourism, we examine views and practices in providing inclusive activities and environments. Despite growing stakeholder interest in accessible nature-based tourism, our findings reveal several challenges, including limited knowledge about the consumers, lack of financial resources and long-term planning, and the absence of a holistic accessibility perspective. We discuss these challenges and propose that they can be collectively met through increased stakeholder collaboration for creating accessible nature-based tourism.

Walters, S. (2014). Unruly rhetorics: Disability, animality, and new kinship compositions. PMLA, 129(3), 471-477. DOI: https://doi.org/10.1632/pmla.2014.129.3.471.

“As intersections among rhetoric and composition, disability studies, and animal studies evolve, it will be necessary to develop ways of valuing the unruliness of interspecies- kinship compositions and to foster theories and practices for exploring them” (p. 476-477).

White, M. (2022). Greta Thunberg is ‘giving a face’ to climate activism: Confronting anti-feminist, anti-environmentalist, and ableist Memes. Australian Feminist Studies. DOI: https://doi.org/10.1080/08164649.2022.2062667.

Anti-feminists, anti-environmentalists, and ableists use memes of activist Greta Thunberg, especially representations of her face, to angrily depict her as irrational and a monster. Participants in these interlinked groups create straw versions of feminist activists and distinguish men’s purported rational development of civilisation from emotional girls, women, and nature. Individuals perform such contemptuous operations, as I argue throughout this article, by misrepresenting Thunberg’s climate and feminist platform and shifting the debate from her environmental advocacy to her embodiment and emotions. I closely read these texts and employ academic literature on anti-feminisms, straw arguments, and straw feminisms to suggest how anti-feminists render simplified figurations. Given my consideration of how anti-feminist, anti-environmentalist, and ableist positions are enmeshed in dismissing Thunberg’s activism and physiognomy, I also outline environmental scholarship that addresses gender and disability studies literature on Asperger syndrome and enfreakment. These are complicated critical gestures, but they are necessary since the over 3,000 memes that I studied, and the associated politics, function by simultaneously dismissing girls, women, feminism, the environment, and people with disabilities. Such an analysis of online texts is pressing since anti-feminisms are designed to disqualify feminist thinking about oppression and the vitality of feminist dialogues with related political movements.

Wolbring, G. (2019, October 21). A culture of neglect:  Climate discourse and disabled people. In A. Gorman-Murray & G. Gordon Waitt (Eds.), Climate [Feature Issue]. M/C Journal, 12(4). DOI: https://doi.org/10.5204/mcj.173.

“The scientific validity of climate change claims, how to intervene (if at all) in environmental, economic, political and social consequences of climate change, and the adaptation and mitigation needed with any given climate change scenario, are contested areas of public, policy and academic discourses. For marginalised populations, the climate discourses around adaptation, mitigation, vulnerability and resilience are of particular importance. This paper considers the silence around disabled people in these discourses.”

Wolbring, G. (2013). Ecohealth through an ability studies and disability studies lens. In M. K. Giaslason (Ed.), Ecological Health: Society, Ecology and Health [Vol. 15], (pp. 91-107).  Emerald: London, UK. Available: http://hdl.handle.net/1880/49856.

Purpose – The goal of this chapter is to cultivate interest in the societal dynamic of ability expectations and ableism, a dynamic first thematized by the disabled people rights movement but which is also broadly applicable to the study of the relationship between humans, animals, and environments. Another aim of this chapter is to think about disabled people within ecosystem approaches to health through the ableism framework and to show that insights gained from disability studies are applicable to a broader study of health within contexts of environmental degradation. Building from this approach, the reader is invited to consider the utility of the conceptual framework of eco-ability ‘expectations’ and eco-ableism as a way to understand health within coupled social- ecological systems. Methodology/approach – This chapter uses an ability expectation and ableism lens and a disability studies and ability studies approach to analyze the relationship between humans, animals, and environments. Findings – Certain ability expectations and ableism are responsible for (a) the invisibility of disabled people in ecological health discourses; (b) the standoff between anthropocentric and biocentric/ecocentric approaches to health; and (c) the application of scientific and technological advancements to address problems arising out of current relationships between humans, animals, and environments. Originality/value of chapter – The reader is introduced to the concepts of ableism and eco-ableism, which have not yet been used in EcoHealth discourses and flags the need for further engagement with disability issues within the field.”

Wong, A. (2019). The rise and fall of the plastic straw: Sucking in Crip defiance. In K. Fritsch, A. Hamraie, M. Mills, & D. Serlin (Eds.), Special Section on Crip Technoscience. Catalyst: Feminism, Theory, Technoscience, 5(1), 1-12. DOI: https://doi.org/10.28968/cftt.v5i1.30435.

A personal essay on the recent efforts to ban single use plastic straws, and how this ban is problematic for disabled people.

Wong, S., Rush, J., Bailey, F., & Just, A. C. (2023). Accessible Green Spaces? Spatial Disparities in Residential Green Space among People with Disabilities in the United States. Annals of the American Association of Geographers, 113(2), 527-548. DOI: https://doi.org/10.1080/24694452.2022.2106177.

This article presents new quantitative results on the distribution of residential green space for people with disabilities in the United States, building on and bridging scholarly research in two distinct domains: one involving approaches that quantify disparities in green space access among racialized minorities and socioeconomically disadvantaged groups, and the other using qualitative methods that demonstrate that most green spaces remain inaccessible and unwelcoming to disabled visitors. Using generalized additive models (GAMs) that controlled for demographic factors and climatological characteristics, we find that residential areas with more green space generally have a higher proportion of disabled residents. The statistical results run counter to expectations from the literature, thus complicating the prevailing narrative and indicating a need for mixed-methods research to examine multiple dimensions of access and environmental justice. Using cluster analysis to assess spatial trends, we detect residential clusters of high disability and low green space and find that they are located in predominantly non-White, urban, and more socioeconomically disadvantaged neighborhoods compared to clusters of high disability and high green space. Cluster analysis results suggest that there are inequities in green space access at the intersection of disability, race, and class, as well as across the urban–rural continuum.

The World Bank. (2023, October). Climate Change and Disability Inclusion in Uzbekistan. DOI:
https://doi.org/10.1596/40538. Washington, DC: Author.

The impacts of climate change will be unevenly felt within and across countries partly due to social and economic inequalities. Persons with disabilities represent 16 percent of the global population and face widespread forms of social and economic marginalization yet have received little attention in prior studies of climate change and social inequality. The mortality rate of persons with disabilities in natural disasters is “up to four times higher than people without disabilities” (Stein and Stein 2021). How do the fast-moving shocks, flooding, drought, heatwaves and slower-moving social and economic effects of climate change impact persons with disabilities How can climate change adaptation efforts be disability inclusive This study examines these questions through original fieldwork and qualitative interviews conducted in Uzbekistan. In November 2022, the authors interviewed persons with disabilities in three regions of the country. The resulting qualitative data afford key insights into how climate change and disability status interact to generate distinct vulnerabilities. Within the nascent field of climate change and disability studies, this report represents one of the first fieldwork-based accounts of how climate change presents heightened risks to persons with disabilities in a developing country context.

Ziarkowska, J. (2022). Cherishing the Impaired Land: Traditional Knowledge and the Anthropocene in the Poetry of Gwen Westerman. In M. Premoli & D. Carlson (Eds.), Indigeneity and the Anthropocene II [Special Issue]. Transmotion, 8(1). DOI: https://doi.org/10.22024/UniKent/03/tm.1007.

In the article I propose to read the work of Sisseton Wahpeton Oyate poet Gwen Westerman from the perspective of environmental humanities and disability studies. Following the insights of Heather Davis and Zoe Todd, I would like to indigenize the field by emphasizing the importance of traditional Indigenous knowledge in the responses to the effects of the Anthropocene. In Westerman’s poetry, the Anthropocene and the accompanying destruction of the environment begin with settler colonialism, which has more serious consequences than the ecological crisis: the loss of traditional lifestyles, foodways, and languages. If Westerman’s speakers believe in Indigenous survival, it can be found in the preservation of traditions and attention to/care for the land that is polluted, altered, and in pain. The emphasis on the need to return the land to the state of balance stands in sharp contrast with the way the discourse of capitalism describes the polluted environment as overexploited, useless, and “impaired.” As Sunaura Taylor has eloquently argued in her presentation “Disabled Ecologies: Living with Impaired Landscapes”, such a use of the “impaired” modifier demonstrates the extent to which Western preoccupation with and privileging of ableism – able bodies which are productive under capitalism – has penetrated thinking about damaged environments. Again, in Westerman’s work, “impairment” is an invitation to  a relationship with the land and its human, non-human, and inanimate beings. The condition of environmental change and pollution necessitates a new understanding of this relationship rather than its abandonment due to the capitalist logic of profit accumulation.

Zúñiga, D (2020). To think and act ecologically: The environment, human animality, nature.  Critical Review of International Social and Political Philosophy Online Before Print. DOI: https://doi.org/10.1080/13698230.2020.1772605.

Much work in care ethics and disability studies is concerned with the flourishing of human animals as an independent species. As a result, it focuses on how the built environments and the social structures that produce them restrict and exclude us. This paper addresses this problem and provides tentative first steps towards sketching an account of ethics that is structured around the interdependent nature of human and more than human life. I argue that our embodied existence places us in a shared condition of vulnerability with all forms of life on earth. This allows us to conceive of caring as an essential condition of the sustainability and well-being of social and ecological life systems. To this end, I discuss the notion of anthropocentrism – and the attendant notion of Anthropocene – and argue that the conception of human animality that underwrites it posits a disembodied and homogenous ‘anthropos’ that is equally responsible for and equally affected by unsustainable social systems. Further, I examine the debate that opposes realist and constructivist accounts of nature, and I argue that it is inadequate to look at nature through the lenses of the predatory social systems that are responsible for ecological injustices in the first place.

OIPO Disability Abstracts: Entrepreneurship

Updated 7/26/2023

Baines, N., & Klangboonkrong, T. (2021, April). Disability entrepreneurship research: Review and critical reflection through the lens of individual-opportunity nexus [CIMR Research Working Paper Series No. 51]. London: Centre for Innovation Management Research, School of Business, Economics & Informatics, Birbeck University of London.

Given the paucity and the fragmented nature of the extant literature on disability entrepreneurship, this literature review juxtaposes the current body of knowledge to the individual-opportunity nexus perspective on entrepreneurship. Six thematic findings emerge from the review. Together, they suggest that while the term disability is understood in relation to structural hindrances and that barriers on multiple levels – societal, market, and personal – influence the availability of opportunities to entrepreneurs with disability (EWDs), current understanding of how these challenges could be overcome is mostly related to adaptive mechanisms at the individual level. The use of individual-opportunity nexus as the point of departure reveals some limitations, as we argue that the deterministic, variance-theoretic approach may be too restrictive if entrepreneurship is intended as a development policy. The same concern will likely apply to other areas of entrepreneurship involving disadvantaged people. Some future research avenues that contribute to both theory and practice are suggested.

Balcazar, F. E., Kuchak, J., Dimpfl, S., Sariepella, V., & Alvarado, F. (2014). An empowerment model of entrepreneurship for people with disabilities in the United States. Psychosocial Intervention, 23, 145-150. DOI: https://doi.org/10.1016/j.psi.2014.07.002.

People with disabilities are greatly underrepresented in the workforce, often face discrimination by employers, and often are not effectively served by the U.S. Vocational Rehabilitation System whose primary purpose is to get individuals with disabilities employed. Additionally, many individuals with disabilities face discrimination and/or fear of becoming a liability by business owners. The Chicago Add Us In (AUI) Initiative sponsored by the U.S. Department of Labor, Office of Disability Employment Policy, created an entrepreneurship program for people with disabilities in order to counteract these barriers, promote empowerment and facilitate economic self-sufficiency for people with disabilities. The model includes a course on how to write a business plan, one-on-one business mentoring, technical assistance, start-up business grants, and assistance from a business incubator. In addition to the core program components, there was an emphasis on creating systems change in the Illinois Division of Rehabilitation Services (DRS) to ensure program sustainability. In-depth case studies are offered to illustrate the process of consumer empowerment and the impact of the entrepreneurship program on the lives of the entrepreneurs who have participated thus far.

Balcazar, F. E., Murthy, S., Gibbons, T. M., Sefandonakis, A., Renko, M., Parker Harris, S., & Caldwell, K. (2023). Supports and barriers that entrepreneurs with disabilities encounter when starting their businesses. Rehabilitation Psychology, 68(1), 91–101. DOI: https://doi.org/10.1037/rep0000479.

Purpose/Objective: Entrepreneurship is increasingly emerging as a viable employment option for many people with disabilities. It provides opportunities to develop interests, skills, and passion for starting a business. We conducted multiple interviews with various stakeholders to identify the perceived supports and barriers that people with disabilities encounter in the process of pursuing entrepreneurship. Research Method/Design: Individual interviews included 20 entrepreneurs with disabilities, 6 service providers, and 5 school administrators. This qualitative study used a constructivist grounded theory approach to shape the process of data collection, analysis, and theory building. Results: People with disabilities interested in pursuing entrepreneurship benefit from facilitators such as social support, mentoring, and access to space, equipment, and money. Personal qualities include their desire to be “my own boss,” help others, earn money, creativity, persistence, and flexibility. On the other hand, they may face several systemic barriers, such as the lack of infrastructure to set up the business, discrimination, lack of formal support from Vocational Rehabilitation counselors or their school settings, and/or lack of money. Conclusions/Implications: The systemic barriers can make it difficult for entrepreneurs to start and/or continue to operate their businesses. We discuss the implications of the findings for the development of entrepreneurship training for youth with disabilities and offer recommendations for future research and practice in the rehabilitation field.

Barba-Sánchez, V., Ortíz-García, P., & Olaz-Capitán, A. (Eds.). (2019). Entrepreneurship and Disability [Special Issue]. Journal of Entrepreneurship Education, 22(2).

The studies included in this Special Issue feature research on the identification of those competencies that promote or limit entrepreneurship of people with disabilities.

Barba-Sánchez, V., Salinero, Y., Jiménez Estévez, P. and Ruiz-Palomino, P. (2023). How entrepreneurship drives life satisfaction among people with intellectual disabilities (PwID): A mixed-method approach. Management Decision Ahead-of-Print. DOI: https://doi.org/10.1108/MD-11-2022-1568.

Purpose: The high and persistent unemployment rates of people with intellectual disabilities (PwID) reveal the wide gap that still remains to be bridged. Entrepreneurship combinedly with a high enterprising tendency could improve PwID’s life satisfaction.

Design/methodology/approach: A mixed-method approach was used, based on questionnaires and structured face-to-face interviews on 37 PwID who had recently become entrepreneurs. Data were firstly quantitatively analyzed using partial least squares-structural equation modelling (PLS-SEM), and qualitative data were used to enable robust findings.

Findings: The entrepreneurial tendency of PwID who had recently become entrepreneurs was found to be a positive to their life quality (LQ), job satisfaction and life satisfaction.

Research limitations/implications: This study revealed that entrepreneurship among PwID who had high enterprising tendency enhances their LQ, job satisfaction and life satisfaction. However, further research could evaluate whether becoming an entrepreneur is in itself enough to change PwID’s life to better, such that a comparison could be done between PwID who become entrepreneurs and PwID who have a salaried job.

Practical implications: New aspects in the design of public social policies to improve PwID’s life satisfaction are suggested. These include the facilitation of both entrepreneurship and enterprising tendency for PwID to enhance their life satisfaction.

Originality/value: There are very few occasions in which PwID set up businesses. This is one of the first studies to analyze the benefit of entrepreneurship and enterprising tendency on the LQ, the satisfaction at work and the life satisfaction of PwID.

Bennett, D., & Gibb, Y. K. (2022). Entrepreneurship, neurodiversity & gender: Exploring opportunities for enterprise and self-employment as pathways to fulfilling lives. Bingley, UK: Emerald Publishing Limited. DOI: https://doi.org/10.1108/9781800430570.

Entrepreneurship, Neurodiversity & Gender shines a spotlight on issues of intersectionality and opens the debate on how we can develop and support the options of entrepreneurship or self-employment that are offered to young people early on in their career.

Boellstorff, T. (2019). The opportunity to contribute: Disability and the digital entrepreneur. Information, Communication & Society, 22(4), 474-490. DOI: https://doi.org/10.1080/1369118X.2018.1472796.

A range of scholarly work in communications, informatics, and media studies has identified ‘entrepreneurs’ as central to an emerging paradigm of digital labor. Drawing on data from a multi-year research project in the virtual world Second Life, I explore disability experiences of entrepreneurism, focusing on intersections of creativity, risk, and inclusion. Since its founding in 2003, Second Life has witnessed significant disability participation. Many such residents engage in forms of entrepreneurship that destabilize dominant understandings of digital labor. Most make little or no profit; some labor at a loss. Something is being articulated through languages and practices of entrepreneurship, something that challenges the ableist paradigms that still deeply structure both digital socialities and conceptions of labor. Disability is typically assumed to be incompatible with work, an assumption often reinforced by policies that withdraw benefits from disabled persons whose income exceeds a meagre threshold. Responses to such exclusion appear when disabled persons in Second Life frame ‘entrepreneur’ as a selfhood characterized by creativity and contribution, not just initiative and risk. In navigating structural barriers with regard to income and access, including affordances of the virtual world itself, they implicitly contest reconfigurations of personhood under neoliberalism, where the laboring self becomes framed not as a worker earning an hourly wage, but as a business with the ‘ability’ to sell services. This reveals how digital technology reworks the interplay of selfhood, work, and value – but in ways that remain culturally specific and embedded in forms of inequality.

Caldwell, K., Parker, S., & Renko, M. (2016, January). Social entrepreneurs with disabilities: Exploring motivational and attitudinal factors. Canadian Journal of Disability Studies (CJDS), 5(1), 211-244.

The current economic climate demands more innovative approaches to increasing labor market participation for people with disabilities. Social entrepreneurship offers one alternative pathway to employment. However, little is known about the motivational and attitudinal factors influencing social entrepreneurship for people with disabilities. Using empirical data from focus groups comprised of social entrepreneurs with disabilities, and interviews with key stakeholders working in the fields of policy, disability, and business, this research frames its analysis in the intersection of disability studies and entrepreneurial studies to explore: what motivates people with disabilities to pursue social entrepreneurship, if they continue to encounter attitudinal barriers and discrimination, and whether motivational and attitudinal factors affect their social entrepreneurship. Findings indicate that despite social entrepreneurship having been promoted as a strategy for circumventing employment discrimination, the individuals with disabilities in this research continued to encounter attitudinal barriers and discrimination affecting their employment decisions. Future research should focus on interrogating what might be gained in the spaces where need and opportunity intersect and exploring the extent to which motivations overlap for social entrepreneurs with disabilities in theory, policy, and practice.

Caldwell, K., Parker Harris, S., & Renko, M. (2017). Women, disability, and entrepreneurship. In C. Henry, T. Nelson, & K. V. Lewis (Eds.), The Routledge Companion to Global Female Entrepreneurship (pp. 327-341). New York: Routledge.

Within a global context, entrepreneurship for people with disabilities differs significantly among regions, depending upon international and national policy efforts. In the UK the advancement of the ‘Learning Society’ has led to the promotion of developing entrepreneurial skills in education, but not necessarily materially supporting small business development (Pavey, 2006). The history of disability and institutionalization is distinct in many European countries, where an entire generation was lost to the Eugenic influences of the second World War (Mitchell & Snyder, 2003). This has been reflected in their employment programs, which vary substantially: from truly innovative approaches to inclusion to regressive approaches that further segregate people with disabilities. While rates of people with disabilities in self-employment vary widely among Member States within the European Union, community integration has been a strong mandate in current policy that indirectly supports entrepreneurship as a strategy under the broader umbrella of participation in employment (Halabisky, 2014). In developing countries, entrepreneurship has been used as an anti-poverty strategy to help individuals with disabilities and communities in remote regions (van Niekerk, Lorenzo, & Mdlokolo, 2006). Given that Article 27 of the United Nations Convention on the Rights of Persons with Disabilities (UNCRPD) explicitly identifies self-employment and entrepreneurship as a right, it is expected that there will be continued growth in this area across the world. However, it is unclear how change might be implemented or evaluated on an international scale. For example, in India there has been some controversy surrounding the implementation of micro-enterprise programs that are intended to support entrepreneurship but instead promote a neoliberal agenda that further disadvantages people with disabilities (Chaudhry, 2012). However, such claims demand further research, especially as pertaining to gender.

Caldwell, K., Parker Harris, S., & Renko, M. (2020, March). Inclusive management for social entrepreneurs with intellectual disabilities: “How they act.” Journal of Applied Research in Intellectual Disabilities, 33(2), 204-218. DOI: https://doi.org/10.1111/jar.12662.

Background: Social entrepreneurship is a growing trend that reflects a shift in contemporary policy towards entrepreneurship and self-employment as viable employment option for people with disabilities. Entrepreneurship is intended to promote autonomy and reduce dependence on entitlement-based services as well as reduce employment disparities while stimulating business and job creation. However, it is not well understood what exactly this means for people with intellectual disabilities (ID) involved in social entrepreneurial ventures.
Methods: Dyadic interviews were conducted with people with ID participating in social entrepreneurship (n = 7) as well as with the person they identified as instrumental in providing support (n = 7). Interviews focused on understanding the management processes used by people with ID, or “how they act” in negotiating between formal and informal systems of services and supports and barriers encountered.
Results: Themes that emerged include the main barriers they experienced, how their businesses are organized; and the use of formal and informal services and supports.
Conclusions: This research expands upon our understanding of social entrepreneurship and the management processes involved in customized employment for people with ID. It offers new insights and information for practitioners, policymakers, and researchers to inform the expectations we set for entrepreneurship as a sustainable employment option, from the perspective of social entrepreneurs with ID themselves.

Caldwell, K., Parker Harris, S., & Renko, M. (2020). Inclusive entrepreneurship and motivation among people with intellectual disability: “Why they act.” Intellectual and Developmental Disabilities, 58(6), 499–512. DOI: https://doi.org/10.1352/1934-9556-58.6.499.

Social entrepreneurship is a growing trend for people with intellectual disability (ID). This trend reflects a shift in contemporary policy towards entrepreneurship and self-employment as a viable employment option for people with disability in general; a strategy which is intended to promote autonomy and reduce dependence on entitlement-based services as well as to reduce employment disparities and stimulate business and job creation. However, it is not well understood what exactly this means for people with ID involved in social entrepreneurial ventures. This research approached the issue by conducting dyadic interviews to explore the motivations of people with ID who are participating and supported in social entrepreneurship—“why they act.” In exploring these motivations, this article investigates push-pull factors, the role of the social mission, and how support influences motivation.

Casado, A. B. F., & Casau, P. M. (2019). Personal self-knowledge, a key factor for entrepreneurship in people with disabilities. Journal of Entrepreneurship Education, 22(S2).

The article hereby analyses the influence of psychological factors on entrepreneurship of people with disabilities, focusing on the dimension “Personal Self-knowledge”. Its aim is to look into the extent of such an influence on this collective when launching an entrepreneurial activity as well as to know both, the competence self-evaluation in people with disabilities and the factors or barriers, which in their opinion limit such entrepreneurship. The data used in this article are the result of a survey which was conducted between November and December 2018 on a sample of residents in Spain who have physical, sensory and organic disabilities. The technical sheet of such survey appears referenced in the Article of Barba-Sánchez, published in this review. It was developed by the University of Murcia within the framework of the Project “Disability and entrepreneurship.

Dakung, R. J., Bell, R., Orobia, L. A., & Yatu, L. (2022, November). Entrepreneurship education and the moderating role of inclusion in the entrepreneurial action of disabled students. The International Journal of Management Education, 20(3), 100715. DOI: https://doi.org/10.1016/j.ijme.2022.100715.

Educators and policymakers have sought to open entrepreneurship to a broader range of students. The paper investigates the role of entrepreneurship education in the development of People with Physical Disabilities (PWPDs) and the moderating role of inclusion in their entrepreneurial action. This research employed a cross-sectional survey of 253 students with physical disabilities across tertiary institutions in Nigeria. The findings underscore the significant role of entrepreneurship education in enhancing the entrepreneurial action of physically disabled students. The finding of the study established the moderating role of inclusion in the relationship between entrepreneurship education and the entrepreneurial action of physically disabled students. This implies that the commitment of the educators to accept and support physically disabled students in the class will create an environment in which physically disabled students can learn to monitor and respond to entrepreneurial changes in the environment. This will in turn prepare them to engage in a business start-up. This research highlights that entrepreneurship education and inclusion make significant contributions to physically disabled students’ entrepreneurial action. Therefore, these factors are key to consider in preparing physically disabled students to become entrepreneurial graduates. The study contributes to the extant literature by underscoring the value of creating an environment of inclusion in entrepreneurship education.

Darcy, S., Collins, J., & Stronach, M. (2020, March). Australia’s disability entrepreneurial ecosystem: Experiences of people with disability with microenterprises, self-employment and entrepreneurship. Broadway, New South Wales: UTS Business School, University of Technology Sydney.

People with disability (PwD) face great difficulty in getting access to the Australian economy. PwD have high unemployment rates while those who do get jobs often find them unsatisfactory. Establishing a business is one strategy to overcome these economic barriers. This report presents the findings of the first detailed research project on PwD self-employed entrepreneurs in Australia. Key findings from this research include: (1) Education: entrepreneurs with disability lamented a lack of entrepreneurial education that may have alleviated common startup mistakes, costing them money, time and emotional energy. When schemes including incubator and accelerator programs are available and accessible, entrepreneurs with disability are likely to benefit. However, mainstream entrepreneurial training programs are not inclusive of disability type nor the level of support needs of EWD; (2) Networking: respondents commented on the difficulty of networking generally, and specifically with other entrepreneurs with disability (EwD); (3) Government social services and bureaucracy: government policies may stifle entrepreneurial activity among those with disability; (4) Culture and attitudes: discrimination in mainstream employment or blocked mobility may push PwD toward self-employment and entrepreneurship. Yet, other barriers may constrain EwD from fostering relationships with consumers, contractors, funders, and other key individuals. Challenging social attitudes about the ability of self-employed and entrepreneurial PwD is required to provide a more level playing field in business for EwD; (5) Importance of family and friendship units: key individuals in the lives of PwD provide support at many levels and are integral in their entrepreneurial journeys, especially so for people pursuing micro-enterprise activities. Many of the cultural, structural and attitudinal barriers experienced by PwD are overcome with support from immediate family, friends and carers; and (6) Financial support: making sure that PwD do not fall into further hardship is crucial in order to foster entrepreneurship in this cohort. Startup progress is contingent on the combination of the human, social and financial capital available for their enterprise. Human and social capital affect access to financial capital. Knowledge and access to mainstream funding opportunities such as in-kind business development, seed funding, grants, angel investors, venture capital, crowd funding or loans should be further developed to support aspiring entrepreneurs with disability.

Darcy, S., Collins, J., & Stronach, M. (2023). Entrepreneurs with disability: Australian insights through a social ecology lens. Small Enterprise Research, 30(1). 24-48. DOI: https://doi.org/10.1080/13215906.2022.2092888.

The study of people with disability who become entrepreneurs has been a neglected field of research but with a developing body of knowledge from different countries around the world over the last two decades. This paper aims to contribute to that body of knowledge through examining the journeys of entrepreneurs with disability (EwD) in Australia. It does so through a theoretical framework guided by the minority entrepreneurship literature, their lived experiences through social model understandings of disability and a social ecology framework. The research design involved interviews with 60 EwD with the findings examining their motivations, barriers, enablers, outcomes and benefits. The discussion examines the social, economic and cultural embeddedness of EwD’s journey, the paradox of their higher rates of entrepreneurship than the nondisabled and the entrepreneurial ecosystem. We conclude by outlining the contribution this study makes to disability entrepreneurship through the complexity revealed by the social ecological framework.

Entrepreneurship Series: Entrepreneurship for People with Disabilities [Accommodation and Compliance Series]. (2018, July). Morgantown, WV: Job Accommodation Network.

This brief document shares two situations and solutions on the issue of entrepreneurship for people with disabilities.

García, P. O., & Capitán, Á. O. (2019). Gender differences in entrepreneurship of people with disabilities. Journal of Entrepreneurship Education, 22(S2).

Data on women and disability in Spain manifest the double discrimination which affects women due to their own condition and the fact of presenting some kind of disability. This situation of vulnerability is especially evident in the labour field, in general, and in self-employment or entrepreneurship, in particular. Basing on a survey conducted on this collective concerning this issue, this article inquires about the differences in entrepreneurial activity among people with disabilities in relation to gender. The results show the lower propensity of women to start up a business in comparison to men. According to such data, differential aspects in entrepreneurial motivation and in the factors that inhibit such activity are also identified.

Győri, Z., Svastics, C., & Csillag, S. (2019). Conference Paper: Push and Pull Motivations of Entrepreneurs with Disabilities in Hungary. In Tipurić, Darko Hruška, Domagoj (Eds.), 7th International OFEL Conference on Governance, Management and Entrepreneurship: Embracing Diversity in Organisations. April 5th – 6th, 2019, Dubrovnik, Croatia, Governance Research and Development Centre (CIRU), Zagreb (pp. 351-366).

Disability is a worldwide phenomenon: approximately 16% of the world’s adult population aged 18 and older is disabled. WHO terms disability as an umbrella term, covering impairments, activity limitations and participation restrictions, including participation in the labour market. One possible solution to problems of low rates of labour market participation could be for people with disabilities to become entrepreneurs and run their own businesses. In our paper we would like to contribute to the growing body of empirical research on entrepreneurs with disabilities, highlighting the results of our exploratory qualitative research project, with a focus on ten Hungarian entrepreneurs with sight loss and physical disabilities. We explore and analyse the motivational background of people with disabilities establishing their own enterprises, showing forms of pull and push motivation.

Hafiar, H., Subekti, P., Setianti, Y., & Asiah, N. (2021, March). Mapping of research publications concerning disabilities and entrepreneurs as scientific communication activities. NYIMAK Journal of Communication, 5(11), 117-133. DOI: http://dx.doi.org/10.31000/nyimak.v5i1.3664.

Limited availability of employment opportunities, making some with disabilities intend to become entrepreneurs. There are a number of research results related to disability and entrepreneurship that have been published and indexed on the Garuda portal. The publication of research results is one of the scientific communication activities. This research aims to map a number of these studies. The research method used is descriptive quantitative. Based on the results of the analysis, it is known that research related to disabilities and entrepreneurship which is published in national journals and indexed on the Garuda portal, the majority of the research content makes the disability community the subject of its study, is followed by disabled entrepreneurs and students with disabilities, and makes people with disabilities in general the subject of their studies. followed by hearing, physical, visual and intellectual disabilities. Furthermore, there are four clusters of keywords related to the results of disability and entrepreneurial research. The first cluster of entrepreneurs is associated with training, education, ability, motivation, and finance. The second cluster of entrepreneurship is associated with skills, vocational, character, independence and marketing. The third cluster, entrepreneurship, is associated with mentoring, empowerment, business and community. The fourth cluster connects entrepreneurship with, welfare, accessibility, economy and entrepreneurs.

Halabisky, D. (2014). Policy Brief on Entrepreneurship for People with Disabilities: Entrepreneurial Activities in Europe. Paris: Organisation for Economic Cooperation and Development (OECD).

This paper is part of a series of policy briefs on inclusive entrepreneurship produced by the OECD Local Economic and Employment Development Programme and the European Commission Directorate-General for Employment, Social Affairs and Inclusion.

Hidegh, A. L., Svastics, C., Csillag, S., & Győri, Z. (2023). The intersectional identity work of entrepreneurs with disabilities: Constructing difference through disability, gender, and entrepreneurship. In J. Mahadevan, H. Primecz, & A. J. Mills (Eds.), The politics of difference: Critical investigations across time and space [Special Issue]. Culture and Organization, 29(3), 226-241. DOI: https://doi.org/10.1080/14759551.2023.2201006.

Despite a growing interest in intersectional entrepreneurship studies investigating the interplay of privileged and disadvantaged identities, people with disabilities still appear to be a ‘forgotten minority’ in that field. Drawing on qualitative interviews with 29 entrepreneurs with disabilities (EWD), this study examines how differences are constructed by EWD when performing intersectional identity work at the crossroads of disability, gender, and entrepreneurship. The results revealed four overlapping strategies in response to different sources of identity threats, such as disability and gender threats: bracketing, reconciling, adjusting, and neglecting. While the identity work of EWD was informed by challenging dominant entrepreneurial discourse impregnated by ableism and hegemonic masculinity, simultaneously, othering was also used in crafting positive identities, which instead reproduced power-laden social differences.

Hsieh, Y., Josse Molina, V., & Weng, J. (2019, December). The road to entrepreneurship with impairments: A challenges-adaptive mechanisms-results model for disabled entrepreneurs. International Small Business Journal: Researching Entrepreneurship, 37(8), 761–779. DOI: https://doi.org/10.1177/0266242619867654.

This article explores how different challenges potentially inspire those deemed impaired to engage with entrepreneurship and how they overcome such challenges through different adaptive mechanisms. Taking an interpretive perspective, we undertook semi-structured interviews with 13 entrepreneurs with impairments, providing an understanding of the relationship between challenges and the adaptive mechanisms that led to business and personal attainments. Based on our empirical findings, we propose a new challenges-adaptive mechanisms-results (CARE) model contributing to the literature on disabled entrepreneurship among those with impairments and also provide insights into the entrepreneurial endeavours of the disabled population.

Hutchinson, C., Lay, K., Alexander, J., & Ratcliffe, J. (2021, March). People with intellectual disabilities as business owners: A systematic review of peer-reviewed literature. Journal of Applied Research in Intellectual Disabilities, 34(2), 459-470. DOI: https://doi.org/10.1111/jar.12836.

Background: Microenterprises are very small businesses requiring little capital and can be an employment pathway for people with intellectual disabilities. This systematic review aims to identify the facilitators, barriers and outcomes from microenterprise.
Method: Web of Science, Scopus, EconLit, PsycINFO and ProQuest were searched to identify peer-reviewed studies on microenterprises owned by people with intellectual disability published up to and including 1 October 2019.
Results: A total of 1080 papers were independently screened by two reviewers. Six papers met the inclusion criteria. Barriers included lack of access to business expertise and resources, and the tension between growing microenterprises and maintaining eligibility for welfare payments. Formal and informal supports were key facilitators. Outcomes experienced included additional income, skills development, increased confidence and engagement in meaningful activities.
Conclusion: Additional research is required to develop an evidence base which may support investment in this employment pathway, making microenterprise more accessible to people with intellectual disabilities.

Jammaers, E., & Williams, J. (2021). Turning disability into a business: Disabled entrepreneurs’ anomalous bodily capital. Organization. DOI: https://doi.org/10.1177/13505084211032312.

In a time and place where being impaired is equated to being of lesser economic value, some disabled people take matters into their own hands by creating their own job and converting their bodily difference into bodily capital. This paper uses a Bourdieuan lens to discover what sets apart disabled entrepreneurs who build their business around disability and those who do not. Building on the experiences of 40 entrepreneurs, we outline the existence of certain bodily and mental schemata that lead to a body habituated to run a business centred around one’s impairment and experience of living as a disabled person in an ableist world. We specify such ‘anomalous’ bodily capital and discuss the constraints to its conversion related to the social environment and impairment effects. This study speaks back to the literature on disability in organizational contexts by extending the ‘value in disability’ debate whilst remaining cognizant of the danger of ‘supercrip’ stereotyping and disability ghettoization. In addition, the complex structure/agency interplay inherent to the practice of leveraging anomalous bodily capital offers a contribution to entrepreneurship research that tends to adhere to a simplistic view of the body.

Jammaers, E., & Zanoni, P. (2020): Unexpected entrepreneurs: The identity work of entrepreneurs with disabilities. Entrepreneurship & Regional Development An International Journal, 32(9-10), 879-898. DOI: https://doi.org/10.1080/08985626.2020.1842913.

Drawing on in-depth interviews, this study investigates how entrepreneurs with disabilities (EWDs) position themselves, in their identity work, vis-à-vis dominant, normative representations of the entrepreneur that tend to exclude them. Addressing the current neglect in how EWDs deal with such discursive barriers, we document four identity positions which they deploy, in various combinations, to construct an identity as an entrepreneur. Our findings show that outward positions, by which EWDs compare their own self with (non)-entrepreneurial (able-bodied) others and emphasize similarity and uniqueness, reproduce normative representations of the entrepreneur. Inward positions, by which EWDs engage in inner conversations contrasting their current self with older, aspirational or impossible selves, on the contrary lead to the destabilization of normative representations. This study speaks back to wider debates in entrepreneurship studies, including the plea to consider ‘ordinary’ entrepreneurs, the difference between ‘being’ an entrepreneur and ‘doing’ entrepreneurship, and the value in difference.

Kašperová, E. (2021). Impairment (in)visibility and stigma: How disabled entrepreneurs gain legitimacy in mainstream and disability markets.
Entrepreneurship & Regional Development, 33(9-10), 894-919. DOI: https://doi.org/10.1080/08985626.2021.197410.

Entrepreneurs’ use of linguistic practices, such as storytelling, in building legitimacy with customers and others is well documented. Yet, not all entrepreneurs may equally use or benefit from such practices in their legitimacy-building efforts. For those with stigmatized social identities, like disability, embodied properties and practices of non-linguistic, more visual kind, may be salient despite being under-explored in the entrepreneurial legitimacy studies. To address this knowledge gap, this article examines how disabled entrepreneurs gain legitimacy with customers and, more specifically, how impairment visibility shapes their capacity to do so. Drawing primarily on in-depth interviews with UK-based entrepreneurs, the article extends Suchman’s work by reconceptualizing his legitimacy-building strategies considering impairment visibility. It is argued that impairment visibility can both enable and constrain legitimacy depending on the product offering and the target market. Disabled entrepreneurs are found to adopt four embodied legitimacy-building strategies in the marketplace, each with specific implications for their micro-level interactions with customers.

Kitching, J. (2014). Entrepreneurship and Self-Employment by People with Disabilities [Background Paper for the OECD Project on Inclusive Entrepreneurship]. Paris: Organisation for Economic Cooperation and Development (OECD).

“The objective of this background paper is to examine the possibility that entrepreneurship – defined as self-employment or business ownership – offers a solution to disabled people’s labour market disadvantage and social exclusion” (pp. 1-2).

Krüger, D, & David, A. (2020, February). Entrepreneurial education for persons with disabilities—A social innovation approach for inclusive ecosystems. Frontiers in Education, 5(3). DOI: https://doi.org/10.3389/feduc.2020.00003.

Fostering entrepreneurship and inclusive societies are on top of EU policy agenda. This article is bringing together both aims by discussing a social innovation framework for inclusive entrepreneurial education for persons with disabilities. Similar to other disadvantaged groups, persons with disabilities can benefit from entrepreneurial skills for self-management or, on a next level, for starting own, opportunity-driven businesses. The framework suggests several building blocks considered necessary for successful entrepreneurial education for the beneficiaries. First, it is approaching the framework through a social innovation perspective. In doing so, it suggests a social innovation ecosystem perspective to operationalize all relevant stakeholders and contextual aspects relevant for the framework. Second, it suggests to build on socially innovative, hence novel, practices by starting from co-creation and co-production in order to meet individual demands and needs of learners. Furthermore, it takes the concept of universal design into account as it holds major implications for inclusive entrepreneurial education for persons with disabilities and underlines the need of different, more suitable practices in entrepreneurship education and beyond, toward an inclusive learning ecosystem.

Levesque, M. (2020). Leadership as Interpreneurship: A Disability Nonprofit Atlantic Canadian Profile. In C. de Clercy (Ed.), Leadership, Populism and Power [Feature Issue]. Politics and Governance, 8(1), 182–192. DOIhttps://doi.org/10.17645/pag.v8i1.2505.

The entrenchment of the neoliberal state and rise of populist leaders has marginalized the role of voluntary organizations in society. This presents significant challenges for nonprofit leaders in economically challenged areas as it erodes their ability to protect and serve vulnerable populations. Attention turns to maintaining hard fought gains at the expense of making progress. Yet doing so requires new skills and leadership styles to manage organizational change where innovation and transformation are key. Based on 42 qualitative interviews with disability nonprofit leaders in Atlantic Canada, our study aims to characterize this transformation. Using Szerb’s (2003) key attributes of entrepreneurship that distinguish between entre-, intra-, and interpreneurs, we find disability leaders have become interpreneurs. We find a strong emphasis on networked service delivery underscoring shared goals, risks and responsibilities, and resources. For disability leaders, cultivating relationships and strong communication skills are essential. In the face of populist desires for state retrenchment, we question how long this collective response can hold given ongoing economic challenges.

Lundberg, C. S. (2023). Striving to abolish a deficit approach to disability: Frames applied by frontline workers and activist entrepreneurs in employment. Disability & Society. DOI: https://doi.org/10.1080/09687599.2022.2160927.

Frontline workers engaged in enabling employment and activist entrepreneurs strive to reframe disability as they facilitate work inclusion. They do so in an organisational and societal context that emphasises labour-market participation. Frontline workers facilitate this inclusion when they implement and construct disability employment policies at the street level, while activist entrepreneurs do so when they privilege hiring disabled people. Based on interviews in this study within a Norwegian welfare context, I show how both groups of actors strive to abolish a deficit approach in distinct yet overlapping ways. They do so by framing disabled people in terms of their assets and contributions rather than foregrounding their needs and challenges. While the entrepreneurs brought up ways in which disability can be a central part of identity that should be recognised and talked about, the frontline workers promoted assets in an individualised manner. Nevertheless, the deficit approach is maintained in subtle ways.

Matsaure, K., Chindimba, A., Zimano, F.R. & Ruffin, F. (2020). Looking under the veil: Challenges faced by people with disabilities in cross border entrepreneurship. African Journal of Disability, 9(0), a645. DOI: https://doi.org/10.4102/ajod.v9i0.645.

Background: Cross-border entrepreneurship is one source of livelihood that is transforming people’s lives, especially those with limited resources and educational qualifications and those in need of supplementary earnings to complement meagre formal earnings. However, despite strides made to make this avenue worthwhile, this Zimbabwean study shows that hidden hindrances still persist from procedural and structural barriers from road entry point management systems. To people with disabilities (PWDs), the impact of these hidden barriers is severe to the extent of obstructing their optimum progression into cross-border entrepreneurship.
Objectives: This article sought to interrogate some veiled challenges in border management systems affecting PWDs’ quest to venture into cross-border entrepreneurship. This angle has, to this end, been timidly addressed as most organisations and legislation have concentrated on making things work for the majority of the populace.
Method: Qualitative phenomenological method in which researchers’ lived experiences, review of literature, ideas and opinions is complemented by secondary survey data from a road entry point management system study in the Zimbabwean setting.
Results: Cross-border entrepreneurship has potential to transform people’s lives: 1) road and border management systems’ procedural and structural complications present hidden challenges impeding PWDs’ entry and optimum participation in cross border entrepreneurship, 2) people with disabilities are not automatically dependents; in fact, most have dependents looking up to the, 30 social construction of disability persists and must be curbed and 4) there is a need to institute a ‘stakeholders triad approach’.
Conclusion: The existing road entry points’ management systems are not informed by considerations from PWDs, hence the existence of hidden challenges. Cross-border entrepreneurship can open significant livelihood avenues to PWDs. A stakeholders ‘triad approach’, proposed herein, can solve some of the policy discrepancies as it recommends utilising inputs from PWDs, research and policy-makers.

Maulida, E., Esty Nurbaity, E., & Utami, V. (2020). Entrepreneurship Education and Entrepreneurial Intention among Disability Students in Higher Education. International Conference on Humanities, Education, and Social Sciences, KnE Social Sciences (pp. 281–289). DOI: https://doi.org/10.18502/kss.v4i14.7886.

Entrepreneurship education helps to form appropriately entrepreneurial mindsets and behaviors in students. This is not only for normal students but also students with special needs in tertiary institutions. This study aims to identify the entrepreneurial intention of students with special needs (disability) at Jakarta State University (UNJ). This research used the case study research method, where the cases are students with disabilities at UNJ who are registered as active students. Data was collected using unstructured interviews. The research revealed three core indicators of student entrepreneurial intention. These are 1) elements of intention (cognition, emotions and conations), 2) characteristics of an entrepreneur and 3) business ethics. The results of this study state that students with disabilities know about entrepreneurship (cognition) and have a desire to become an entrepreneur (emotion) and have experience in trying entrepreneurship (conations). In addition, the students with disabilities also know what needs to be prepared to become an entrepreneur such as the readiness of the risks to be faced and how to run a good business.

Mota, I., Marques, C., & Sacramento, O. (2020), “Handicaps and new opportunity businesses: what do we (not) know about disabled entrepreneurs?” Journal of Enterprising Communities: People and Places in the Global Economy, 14(3), 321-347. https://doi.org/10.1108/JEC-12-2019-0120.

Purpose: The process by which disabled individuals become entrepreneurs can be influenced by factors of different orders. Throughout their entrepreneurship careers and projects, disabled entrepreneurs may have to overcome multiple personal, social and political barriers. This study aims to review what we do (and do not) know about disabled entrepreneurs research to date.

Design/methodology/approach: The literature review focused on analyzing 42 articles from two databases, namely, Web of Science and Scopus. After the articles were selected, they were grouped into thematic clusters.

Findings: The results were categorized into four areas, namely, entrepreneurs with disabilities, self-employment as an alternative to unemployment for people with disabilities, barriers faced by disabled entrepreneurs and the importance of education, training and/or orientation for these individuals’ entrepreneurship. The research verified that, in some cases, people with disabilities resort to self-employment and become entrepreneurs to avoid unemployment. Education and training’s positive role in how this process develops is clear as they empower individuals with disabilities and enable them to raise entrepreneurial attitudes.

Originality/value: Based on the citation profile of articles on disabled entrepreneurs, the results contribute to a better understanding of the flow and main findings of scientific research on this topic over the past 15 years. The findings also include research tendencies that reveal the field’s emergent perspectives, which are of great importance to academics seeking to enhance entrepreneurial processes and policymakers interested in stimulating entrepreneurship education.

Mustaffa, C. S., Halim, H., Ahmad, J., Ishak, M. Q., & Johari, N. A. (2020). Disability and poverty: A review on social entrepreneurship opportunities for persons with disabilities in Malaysia. Albukhary Social Business Journal (ASBJ), 1(2), 1-11. DOI: http://eoi.citefactor.org/10.11241/asbj.01.02.001.

Disability is a phenomenon, which naturally occurs in societies. Just as the able-bodied people, disabled people are part of the society and they form a valuable group, work and participate in economic activities. However, issues on employment among people with disabilities (PWDs), which are viewed as social issues, are still not adequately dealt with even though these issues have long been debated, and are widely discussed. Multiple solutions have been proposed to address these issues but still, members of this group face various obstacles or difficulties in joining the job market. One of the solutions that are seen viable in helping this segment of the community is through social entrepreneurship (SE), which could possibly provide an opportunity to create employment for them. It is anticipated that SE will change the landscape of people with disabilities, and at the same time encourages entrepreneurs with disabilities to participate in economic activities. The urgent call for the implementation of SE is due to the fact that the number of individuals and the unemployment rate among PWDs are now increasing in Malaysia. Thus, this paper elaborates on how SE can be treated as a mechanism in overcoming issues related to PWDs employability in the Malaysian context. This is consistent with the Malaysian Plan of Action for People with Disabilities 2016-2022, which describes the equal rights of PWDs to education, employment, and cultural life; the rights to own and inherit property, not to be discriminated against in marriage, children, and not involving them as unwilling subjects in a medical experiment. The paper provides an opportunity for knowledge sharing on how Malaysia should move forward towards implementing SE program for PWDs.

Norstedt, M., & Germundsson, P. (2021). Motives for entrepreneurship and establishing one’s own business among people with disabilities: Findings from a scoping review. Disability & Society. DOI: https://doi.org/10.1080/09687599.2021.1919504.

As people with disabilities often face difficulties entering the labour market, entrepreneurship and self-employment are often regarded as an opportunity to gain employment and earn a living. This article presents a scoping review that aims to investigate what establishment motives previous studies have identified for self-employment and entrepreneurship among people with disabilities. Four themes emerged: economic motives; flexibility and self-determination; avoiding discrimination; and personal development and being able to contribute something. In the article we discuss the results and relate them to the general discourse on entrepreneurship, which often includes the concept of autonomy. We argue that the findings suggest implications for how to develop support and strategies for this group, to help them avoid ending up in an even more vulnerable position. In this work, the individual’s own motives for establishment are of great value.

Norstedt, M., & Germundsson, P. (2022). Self-employment for people with disabilities: Barriers to and (Im)possibilities in starting and running their own business. Scandinavian Journal of Disability Research, 24(1), 239–252. DOI: http://doi.org/10.16993/sjdr.909.

Little is known about self-employment among people with disabilities in Sweden. The present article contributes knowledge about barriers and opportunities experienced by self-employed people with disabilities and discusses how these affect the labor market inclusion of people with disabilities.

The article draws on qualitative, in-depth interviews with 10 self-employed participants with disabilities and one group interview with six participants who were self-employed and had visual impairments.

The analysis shows that the participants see self-employment as an opportunity for a more flexible working life. However, the economic redistribution on which they often depend to run their business is conditioned in a way that does not take into consideration their everyday life. Consequently, despite political goals of inclusion and social justice, people with disabilities come to be excluded from yet another arena, that is, self-employment.

Office of Disability Employment Policy, U.S. Department of Labor. (2013, December 15). Self-Employment for People with Disabilities. Washington, DC: Author.

ODEP initiated START-UP, a three-year grant project, in 2007 to identify policies and practices then in place that either made it difficult for individuals with disabilities to become self-employed or supported them in becoming self-employed. As part of the initiative, three states (Alaska, Florida, and New York) were awarded grants to pilot new innovative models for assisting individuals with disabilities to start businesses. A fourth grant established a national technical assistance center, Self-Employment Technical Assistance, Resources, & Training (START-UP/USA), to provide information and guidance about promoting self-employment for disabilities to the state grantees, as well as serving as a national resource for individuals and agencies wanting to pursue self-employment goals for people with disabilities. This is the final report of the START-UP initiative. It describes the barriers experienced by the four grantees, the self-employment models tested, the achievements of the grant programs, and case studies of several individuals with disabilities who successfully became self-employed. The report also makes recommendations for adoption by agencies and individuals for realizing self-employment goals.

Pavey, B., Alexander-Passe, N., & Meehan, M. (Eds.). (2020). Entrepreneurship, Dyslexia, and Education: Research, Principles, and Practice. New York: Routledge. DOI: https://doi.org/10.4324/9781351036900.

The development of entrepreneurial abilities in people with dyslexia is a subject of great interest. It has gained increasing importance in economically difficult times because of its potential for the development of new business opportunities. This book brings together contributions from researchers, educators, and entrepreneurs with dyslexia, investigating this subject from many perspectives. Is there something different in the profile of a person with dyslexia that supports the development of entrepreneurship? This book aims to draw out key themes which can be used in education to motivate, mentor, and create the business leaders of tomorrow. It offers a fundamental text for this area of study with a comprehensive, international examination of its topic. It includes views by new and established international writers and researchers, providing up-to-date perspectives on entrepreneurship, dyslexia, and education. It is accessible to read, to understand, and to learn from, and is suitable for recommended reading for graduate and postgraduate students. The diverse views and perspectives demonstrated in this book make it as relevant as possible for a wide group of readers. It informs study in the fields of business and dyslexia, and will be of interest to educators, researchers, and to anyone interested in the overlap of entrepreneurship and dyslexia.

Parker Harris, S., Caldwell, K., & Renko, M. (2014). Entrepreneurship by any other name: Self-sufficiency versus innovation. Journal of Social Work in Disability & Rehabilitation, 13(4), 1-33. DOI: https://doi.org/10.1080/1536710X.2014.961115.

Entrepreneurship has been promoted as an innovative strategy to address the employment of people with disabilities. Research has predominantly focused on the self-sufficiency aspect without fully integrating entrepreneurship literature in the areas of theory, systems change, and demonstration projects. Subsequently there are gaps in services, policies, and research in this field that, in turn, have limited our understanding of the support needs and barriers or facilitators of entrepreneurs with disabilities. A thorough analysis of the literature in these areas led to the development of two core concepts that need to be addressed in integrating entrepreneurship into disability employment research and policy: clarity in operational definitions and better disability statistics and outcome measures. This article interrogates existing research and policy efforts in this regard to argue for a necessary shift in the field from focusing on entrepreneurship as self-sufficiency to understanding entrepreneurship as innovation.

Parker Harris, S., Renko, M., & Caldwell, K. (2013). Accessing social entrepreneurship: Perspectives of people with disabilities and key stakeholders. Vocational Rehabilitation, 38, 35-48. DOI: https://doi.org/10.3233/JVR-120619.

Social entrepreneurship has been gaining increasing attention as a possible employment strategy for people with disabilities. However, little is known about the experiences of social entrepreneurs with disabilities in relation to their resources needs, opportunities for participation, and barriers they encounter. Further, little is understood about how social entrepreneurship differs from self-employment or forms of commercial entrepreneurship. The findings included herein are representative of the first empirical research integrating the fields of disability studies and entrepreneurship studies to explore social entrepreneurship among people with disabilities through interviews with key stakeholders working in the field (n=19) and focus groups with social entrepreneurs with disabilities themselves (n=27). Three themes emerged from this qualitative research that hold particular importance to policymakers and professionals working in the field of vocational rehabilitation: 1) education, training and information; 2) finance, funding and asset development; 3) networking and supports. The findings demonstrate that social entrepreneurship can be an effective model of employment but is currently underutilized. With additional investment, it can offer a meaningful way for people with disabilities to participate in the labor market and complement existing strategies in competitive and customized employment to promote choice and self-determination.

Parker Harris, S., Renko, M., & Caldwell, K. (2014). Social entrepreneurship as an employment pathway for people with disabilities: Exploring political-economic and socio-cultural factors. Disability & Society, 29(8), 1275-1290. DOI: https://doi.org/10.1080/09687599.2014.924904.

The current economic climate demands more innovative approaches to increasing labor market participation for people with disabilities. Social entrepreneurship (SE) offers one alternative employment pathway. However, little is known about the broader factors influencing SE for people with disabilities. Using empirical data from focus groups comprised of social entrepreneurs with disabilities and interviews with key stakeholders working in the fields of policy, disability, and business, this research frames its analysis in the intersection of disability studies and entrepreneurship to explore which factors influence the potential for SE to provide equal participation opportunities for people with disabilities in the labor market. Findings suggest that further consideration of political–economic and socio-cultural factors is needed if we are to better understand the potential of SE for people with disabilities.

Powers, B., Le Loarne-Lemaire, S., Maalaoui, A., & Kraus, S. (2021). “When I get older, I wanna be an entrepreneur”: the impact of disability and dyslexia on entrepreneurial self-efficacy perception. International Journal of Entrepreneurial Behavior & Research, 27(2), 434-451. DOI: https://doi.org/10.1108/IJEBR-06-2020-0400.

This article contributes to the literature on entrepreneurship for people with disabilities through a better understanding of the impact of entrepreneurial self-efficacy perceptions on entrepreneurial intentions in populations with lower levels of self-esteem. It investigates the entrepreneurial intention and self-efficacy of a population of students suffering from dyslexia, which is a learning disability.

Quick Reference Guide: “I can’t work for others anymore.” (n.d.). Washington, DC: National Disability Institute.

This quick reference guide provides information and resources to guide individuals to information on self-employment or entrepreneurship.

Raudsaar, M., & Kaseorg, M. (2013, March). Social entrepreneurship as an alternative for disabled people. GSTF Journal on Business Review (GBR), 2(3), 120-125.

Employment of people with disabilities is an important aspect in terms of social involvement because nonactive residents inhibit economic development. Estonia performs average in comparing ratio of no-active people (including disabled workforce) across EU countries. The situation can be improved when motivation to enter job market is increased either eliminating barriers or applying active employment policy measures. In this regard Estonia has not used its full potential, since intensity of measures taken is relatively modest. However, some good alternatives have emerged among third sector organizations. The main risk groups are women, young people, disabled people and elderly. In this paper we concentrate on the problems of unemployment among disabled people and the aim is to explore alternative work possibilities for disable people. We search for different solutions and analyze cases what has been used in Estonia.

Robinson, S. (2021, Spring). A Black, Dyslexic, Gifted and Male Entrepreneur: The Unheard Voice. Journal of African American Males in Education, 12(2).

Scholarship addressing entrepreneurs who identified themselves as gifted and dyslexia continues to come from a singular perspective and lacks diverse or inclusive views. Researchers examining the experiences of entrepreneurs who are gifted, and dyslexia must include the sociocultural perspectives of Black males and understand the process of how becoming an entrepreneur is based in the individual’s gifted identity. To truly give voice to entrepreneurs from underserved and underrepresented communities, qualitative (i.e., autobiographical) and conceptual research are necessary that focus on new venture creation and development, characteristics, and behaviors. Therefore, this autobiographical article of a Black, dyslexic, gifted male will give voice to the biographical process of becoming an entrepreneur.

Renko, M., & Freeman, M. (2019, December). Entrepreneurship by and for disadvantaged populations: Global evidence. In A. McWilliams, D. E. Rupp, D. Siegel, G. Stahl, & D. Waldman (Eds.), The Oxford Handbook of Corporate Social Responsibility: Psychological and Organizational Perspectives. New York: Oxford University Press.

“In this chapter, we focus on such entrepreneurial entities and draw attention to their ‘actions that appear to further some social good, beyond the interests of the firm and that which is required by law’—that is, the very definition of CSR (McWilliams and Siegel, 2001). More specifically, we focus on the role of entrepreneurship in furthering a distinct form of social good, that is, the integration of disadvantaged populations in the society, and the related provision of economic opportunity to such groups.”

Saxena, S. S., & Pandya, R. S. K. (2018). Gauging underdog entrepreneurship for disabled entrepreneurs. Journal of Enterprising Communities: People and Places in the Global Economy, 12(1), 3-18. DOI: https://doi.org/10.1108/JEC-06-2017-0033.

Purpose: In the past decade, entrepreneurship research has evolved with the contribution of different scholars, but there is a lack of studies available that focused on entrepreneurship with disabilities. The objective of the research is understanding differently abled entrepreneurs and their entrepreneurial journey. How challenges caused by disability contribute to motivate them to pursue entrepreneurship as a career. This study is based on “Underdog entrepreneurs: Challenge-based entrepreneurship model” theoretical model proposed by Miller and Breton-Miller (2017).
Design/methodology/approach: This qualitative research includes case study methodology to study eight differently abled entrepreneurs. All the identified cases are located in the city of Ahmedabad, Gujarat, India. In-depth interviews and multiple visits were scheduled to collect the data. Transcripts of the interview and observation notes were developed for the analysis of the content according to the adopted theoretical model.
Findings: Differently abled entrepreneurs show similar traits as the non-disabled entrepreneurs. They are also found to be more resilient and persistent while dealing with the challenges of failure, stress and uncertainty. Difficult conditions and experiences of discrimination indirectly prepare them for tackling challenges while pursuing entrepreneurship. People close to differently abled entrepreneurs play a critical role in shaping and supporting their ventures.
Research limitations/implications: Owing to the lack of authentic information available on disabled entrepreneurs, the study does not include different entrepreneurs with more disabilities such as hearing impairment, speech impairment and mental illness. The study also focuses on the entrepreneurs of Ahmedabad City, Gujarat because of the similar reason. Originality/value: This paper is an original submission and contributes towards understanding the differently abled entrepreneurs.

Shaheen, G. E. (2016). “Inclusive entrepreneurship”: A process for improving self-employment for people with disabilities. Journal of Policy Practice, 15(1–2), 58–81. DOI: https://doi.org/10.1080/15588742.2016.1109963.

This article describes the theoretical framework, processes, and outcomes associated with a U.S. Department of Labor, Office of Disability Employment Programs (ODEP)-funded project: “Start-UP NY.” Beginning in 2007, ODEP funded three Start-UP projects throughout the United States to test and demonstrate improved practices supporting entrepreneurship among people with diverse disabilities, including those with mental illnesses and veterans with disabilities. The New York project coined the term “Inclusive Entrepreneurship” to describe a model that promoted change at the individual, program, and systems level to improve the rate of small business development by people with disabilities. The author describes the genesis of the project, its intended effects and the lessons learned along the way that resulted in either course corrections or improvements, He then discusses how the project has been sustained and provides recommendations for replicating the project’s approach and methods in other United States communities or in other countries.

Shaheen, G. (2017). Chapter 10: Beyond the business case. In P. Miesing & M. Aggestam (Eds.), Educating Social Entrepreneurs: From Idea Generation to Business Plan Formulation (Vol. 1).  (pp. 97-111). Business Expert Press.

This case provides an example of individual entrepreneurship fur people with disabilities. Social entrepreneurship’s both social and economic goals can be met by seeding and supporting small-scale venture creation that assists people with disabilities to achieve financial stability and improve social inclusion. Social entrepreneurship students who understand the fundamentals of small venture development will benefit from this case. Disability studies students who understand person-centered planning and the employment challenges faced by people with disabilities are also likely to benefit from this case. The optimal benefit may be realized by assigning students of both disciplines as members of the same study teams to better leverage and apply their specific academic knowledge to the case example. After students read through the case, they will answer challenge questions related to the entrepreneur’s personal, venture operational infrastructure, and environmental barriers to a new venture start-up, using an “Inclusive Entrepreneurship Template.” The case exercise provides students with an opportunity to critically examine and discuss how they would assist a prospective entrepreneur with a disability in overcoming the personal, small enterprise infrastructure and environmental challenges that prospective entrepreneurs with disabilities often face in developing or scaling up their new ventures.

Shamir, O. (2015). On sensitivity and disability: Political consumerism, social-political entrepreneurship and social justice. World Political Science, 11(2), 245-277. DOI: https://doi.org/10.1515/wps-2015-1002.

Why do entrepreneurs choose to use consumer power as an alternative political channel in order to create social and political change? What are the conditions that lead them to adopt this strategy? The main purpose of this article is to offer a theoretical framework to discuss political consumerism strategy used by social entrepreneurs, those who seek to influence political norms in society, the conduct of the business market, and the shaping of public policy. The theoretical model, which this article intends to propose, is based on the new institutional approach (Neo-Institutionalism) and on the principles of the rational choice theory. The article suggests an explanatory variable in the form of political consumerism as an alternative means for political participation (alternative politics), which is influenced by structural, political, economic, and cultural conditions as well as by rational cost-benefit calculations made by entrepreneurs. For an empirical study of the proposed theoretical framework, the article analyzes two campaigns where the entrepreneurs employed political consumerism as a primary action strategy to promote issues related to social justice as institutional changes in Israel. The first of these was the campaign launched by the “Bema’agalei Tzedek” (“Paths of Righteousness”) Society for workers’ rights and the rights of the disabled; the second one was the campaign led by the consumer movement known as “Israel Yekara Lanu” against the cottage cheese producers as part of the social protest in the summer of 2011.

Smith, H. L. (2023). Public spaces, equality, diversity and inclusion: Connecting disabled entrepreneurs to urban spaces. In T. de Noronha (Ed.), Public Spaces: Socioeconomic Challenges [Special Issue]. Land, 12(4), 873. DOI: https://doi.org/10.3390/land12040873.

In the UK and in many other countries, the lack of support for disabled entrepreneurs is an economic, cultural, and societal issue. This is because while disabled entrepreneurs belong to and contribute to public spaces, there are often barriers to their full engagement in the local economy. Where interaction is well established, such entrepreneurs add to the cultural richness of places, to personal and societal well-being and economically by wealth creation. The goal of the study is to identify what can be done to overcome the marginalisation of disabled entrepreneurs, which leads to increased local equality of opportunity, thereby adding to the diversity of local economies and, thus, to a more inclusive society. However, as the evidence from this study of the geography of specialised networks which support disabled entrepreneurs in the UK shows, the entrepreneurial capacity of public spaces (inclusive entrepreneurial ecosystems) for disabled entrepreneurs is better in some places and entirely absent in others. It is this local dimension that has been missing in other studies of disabled entrepreneurs. By focusing on the formal networks that have been established to support disabled entrepreneurs rather than the entrepreneurs themselves, the particular knowledge gap that this paper addresses is the importance of the networks in making those connections and bringing about systemic change in urban spaces. They do this in three ways. They provide access to resources that disabled entrepreneurs need to start and grow a business; in turn, they need to engage with other local public and private sector organisations in order to sustain their own activities, and by their role as advocates on behalf of their members through their leadership, they increase the visibility of disabled entrepreneurs within urban spaces. The contribution to academic literature is to explore the interconnection between the agency of particular organisations to improve inclusive entrepreneurial ecosystems and overcome embedded exclusion within urban spaces. Examples from the UK and from the USA provide empirical insights into what can be done.

Svidron, L. M. (2021). Entrepreneurship as an employment option for people with disabilities: Adding information to your job development toolkit. Journal of Vocational Rehabilitation, 54(3), 285-288. DOI: https://doi.org/10.3233/JVR-211138.

BACKGROUND: Traditional job development for people with disabilities involves placement of individuals into currently open community-based positions or customized positions in the community.
OBJECTIVE: When an individual expresses the desire to be self-employed and grow their own business, job developers are unaware of the opportunities available to assist in the process. Entrepreneurship or self-employment has been achieved by many notorious businessmen throughout time. These businessmen all have a disability in which they have learned to embrace their strengths and receive assistance for their weaknesses.
CONCLUSIONS: Lessons can be learned from the top businessmen to assist job developers in developing self-employment and entrepreneurship for their individuals to build a better job development toolbox.

Tihic, M., Hadzic, M., & McKelvie, A. (2021, November). Social support and its effects on self-efficacy among entrepreneurs with disabilities. Journal of Business Venturing Insights, 16, e00279. DOI: https://doi.org/10.1016/j.jbvi.2021.e00279.

We analyze if various programs for entrepreneurs with disabilities (EWD) positively impact their self-efficacy. We examine if variations in self-efficacy of EWD are related to perceptions of social support, quality assistance from service providers, and perceived barriers to entrepreneurship as a way to evaluate the impact of programs for EWD. We draw upon Critical Disability Theory to understand if service providers act as ‘sites of injustice’ for EWD, creating further barriers, or as ‘sites of justice’ that positively impact their self-efficacy. Using a sample of 127 EWD, we find a positive relationship between the services received from entrepreneurship and disability-specific support programs on self-efficacy. Conversely, we find a strong negative relationship between barriers to entrepreneurship and the self-efficacy of EWD. We contribute by forwarding Critical Disability Theory to the realm of entrepreneurship and shedding new empirical light on EWD.

Tucker, R., Zuo, L., Marino, L. D., Lowman, G. H., & Sleptov, A. (2021). ADHD and entrepreneurship: Beyond person-entrepreneurship fit. Journal of Business Venturing Insights, 15, e00219. DOI: https://doi.org/10.1016/j.jbvi.2020.e00219.

Research examining mental health and entrepreneurship has found important links between mental health and entrepreneurship. These findings have led scholars to suggest a fit between some aspects of mental health, and in particular, mental dysfunction, and entrepreneurship. This paper complements extant studies in this area by examining the mental health and entrepreneurship
relationship from a sociocognitive perspective. We examine to what extent does ADHD influence entrepreneurial self-efficacy and opportunity recognition tendency. Our findings are consistent with our hypotheses, suggesting that people with ADHD may not be efficacious in the entrepreneurial context, and specifically in recognizing opportunities. However, confidence in one’s ability regarding the entrepreneurship vocation can grow with education and experience. Our findings allow us to advance theory and offer practical implications.

Uribe-Toril, J., Ruiz-Real, J. L., Ceresia, F., & Valenciano, J. P. (2019). Entrepreneurship and psychological disorders in academic publishing. Journal of Entrepreneurship Education, 22(S2).

The role that different psychological disorders play in entrepreneurial intentions and behaviors is of increasing interest and importance to the scientific community. Scholars have undertaken a range of investigations that demonstrate that individuals with specific psychological disorders should be treated differently to other individuals. Some studies contribute to psychological disorders shifting from a disability paradigm to a paradigm of diversity. The main objective of this work is to carry out a preliminary analysis of the literature published about the relationship between psychological disorders and entrepreneurship. For this purpose, a bibliometric methodology and a fractional counting method of clustering were developed, identifying and analyzing 108 documents as recorded in the Web of Science and Scopus databases on the relationship between entrepreneurship and psychological disorders. This paper represents a contribution to the state-of-the-art of research on entrepreneurship and psychological disorders, identifying trends and proposing future topics and research lines.

Vaziri, D., Schreiber, D., Wieching, R., & Wulf, V. (2014). Disabled entrepreneurship and self-employment: The role of technology and policy building [Background Paper for the OECD Project on Inclusive Entrepreneurship]. Paris: Organisation for Economic Cooperation and Development (OECD).

“…this background paper will illustrate current barriers for disabled people aiming to become an entrepreneur and provide best practice policy examples that support the elimination of these barriers through the application of technology. To conclude, this paper will make recommendations for required policy actions dealing with technology, which will promote disabled people to approach the pathway into self-employment” (p. 2). OECD has a series of policy briefs, short reports designed for policy makers and practitioners. Each policy brief presents key data, policy challenges and policy recommendations on selected themes (visit the OECD website).

Widoyoko, E. P., Setiawan, B., Sholeh, K., & Shina, M. I. (2018). Model of entrepreneurship for people with disabilities. The 1st International Conference on Law, Governance and Social Justice (ICoL GaS 2018), Vol. 54. London: EDP Sciences.

Persons with disabilities are often regarded as unproductive citizens, unable to carry out their duties and responsibilities so that their rights are ignored. Indonesia is a country that has various risks of disability due to various causes, such as prolonged armed conflict, chronic diseases and natural disasters in various areas such as earthquakes, flash floods, landslides and so on. People with disabilities are under-represented in the workforce, often facing discrimination by employers, and often not served and protected effectively. To support the active participation of people with disabilities in society and the economy, this paper aims to explore the role of entrepreneurs with disabilities and the entrepreneurship model of people with disabilities in the study area. We explore entrepreneurial activities between people with disabilities, theoretical foundations, provide entrepreneurial benefits and challenges for people with disabilities, and propose policy recommendations for models of entrepreneurship development with disabilities. Development of entrepreneurship programs for people with disabilities is needed to combat these barriers, promote empowerment and facilitate economic independence for people with disabilities. This model includes courses on how to write business plans, one-on-one business guides, technical assistance, new business grants, and assistance from business incubators.

Williams, J., & Patterson, N. (2019). New directions for entrepreneurship through a gender and disability lens. International Journal of Entrepreneurial Behavior & Research, 25(8), 1706-1726. DOI: https://doi.org/10.1108/IJEBR-12-2017-0499.

Purpose – There is a dearth of studies exploring the intersection of gender and disability within entrepreneurship research. This is despite women’s entrepreneurship research encouraging an expansion of the research questions asked and approaches taken. As a contribution to this debate, the purpose of this paper is to develop an understanding of gender and disability as social categorizations which can shape entrepreneurial opportunities and experiences for disabled women entrepreneurs.

Design/methodology/approach – The paper offers an intersectional conceptual lens for the study of disabled women entrepreneurs to explore a concern for a particular social group – women – at a neglected point of intersection – disability – within the social setting of entrepreneurship. Guided by the research question (how can gender and feminist disability theory contribute to the development of an intersectional theoretical lens for future entrepreneurship research?), the potential for new theoretical insights to emerge in the entrepreneurship field is identified.

Findings – Through a gender and disability intersectional lens for entrepreneurship research, four theoretical synergies between gender and disability research are identified: the economic rationale; flexibility, individualism and meritocracy; and social and human capital. In addition to the theoretical synergies, the paper highlights three theoretical variances: the anomalous body and bodily variation; sexuality, beauty and appearance; and multiple experiences of care as potentially generative areas for women’s entrepreneurship research. The paper identifies new directions for future gender, disability and entrepreneurship research by outlining research questions for each synergy and variance which draw attention to disabled women entrepreneurs’ experiences of choice and control within and across different spaces and processes of entrepreneuring.

Originality/value – The conceptual intersectional lens offered to study disabled women’s entrepreneurship highlights new directions for exploring experiences of entrepreneuring at the intersection of disability and gender. The paper brings disability into view as a social category that should be of concern to feminist entrepreneurship researchers by surfacing different dimensions of experience to those currently explored. Through the new directions outlined, future research can further disrupt the prevailing discourse of individualism and meritocracy that perpetuates success as an individual’s responsibility, and instead offer the potential for richer understandings of entrepreneuring which has a gender and disability consciousness.

Yang, Y., Kulkarni, M., Baldridge, D., & Konrad, A. M. (2022). Earnings of persons with disabilities: Who earns more (less) from entrepreneurial pursuit? Equality, Diversity and Inclusion: An International Journal. DOI: https://doi.org/10.1108/EDI-09-2021-0239.

Purpose – Persons with disabilities (PWD) are among the largest and most diverse minority groups and among the most disadvantaged in terms of employment. Entrepreneurial pursuit is often advocated as a path toward employment, inclusion, and equality, yet few studies have investigated earning variation among PWD.

Design/methodology/approach – The authors draw on social cognitive career theory (SCCT), and the disability employment and entrepreneurship literature to develop hypotheses about who among PWD are likely to earn more (less) from entrepreneurial pursuits. The authors then conduct analyses on the nationally representative sample of the Canadian Survey on Disability (CSD) by including all PWD engaged in entrepreneurial pursuit, and matching each to an organizationally employed counterpart of the same gender and race and of similar age and disability severity (n ≈ 810).

Findings – Entrepreneurial pursuit has a stronger negative association with the earnings of PWD who experience earlier disability onset ages, those who report more unmet accommodation needs, and those who are female.

Originality/value – First, this study applies SCCT to help bridge the literature on organizational employment barriers for PWD and entrepreneurs with disabilities. Second, we call into question the logic of neoliberalism about entrepreneurship by showing that barriers to organizational employment impact entrepreneurial pursuit decisions and thereby earnings. Third, we extend the understanding of entrepreneurial earnings among PWD by examining understudied disability attributes and demographic attributes. Lastly, this study is among the first to use a matched sample to empirically test the impact of entrepreneurial pursuit on the earnings of PWD.

Yousafzai, S., Ng, W., Sheikh, S., & Coogan, T. (2022). Research Handbook on Disability and Entrepreneurship. Cheltenham, UK & Northampton, MA: Edward Elgar Publishing. DOI: https://doi.org/10.4337/9781789905649.

By exploring the economic and social value of disabled people with positive entrepreneurial traits and adaptive skills, this innovative book breaks away from normative entrepreneurial studies to recognise the overlooked value in disabled entrepreneurs.

Image and Audio Description Resources

updated 9/16/2024

Books, Articles, and Chapters

Guidelines and Toolkits

Legislation/Code/Definitions

  • Movie Captioning and Audio Description Final Rule (ADA.gov)  – “ Title III of the ADA requires public accommodations, including movie theaters, to provide effective communication through the use of auxiliary aids and services.  This rulemaking specifies requirements that movie theaters must meet to satisfy their effective communication obligations to people with hearing and vision disabilities unless compliance results in an undue burden or a fundamental alteration.”
  • FCC Guidance on Audio Description – “Audio description (referred to as video description in the Commission’s rules) is audio-narrated descriptions of a television program’s key visual elements. These descriptions are inserted into natural pauses in the program’s dialogue. Audio description makes television programming more accessible to individuals who are blind or visually impaired.” https://www.fcc.gov/consumers/guides/audio-description
  • A guide to understanding and implementing Web Content Accessibility Guidelines 2 – Understanding SC 1.2.5 – Audio Description (Prerecorded): Audio description is provided for all prerecorded video content in synchronized media. (Level AA) “The intent of this Success Criterion (SC) is to provide people who are blind or visually impaired access to the visual information in a synchronized media presentation. The audio description augments the audio portion of the presentation with the information needed when the video portion is not available. During existing pauses in dialogue, audio description provides information about actions, characters, scene changes, and on-screen text that are important and are not described or spoken in the main sound track.”

Media-Specific Guidelines and Resources

Blogs, Podcasts, and Projects

Resources & Publications

Resources

Publications

  • Book cover of "Someone Falls Overboard: Talking through Poems"Someone Falls Overboard: Talking through Poems by Stephen Kuusisto and Ralph James Savarese, “Kuusisto and Savarese explore the meaning of age, disability, poetry, and memory; what emerges is a single long poem about friendship, witty, inventive, profane.” –George Estreich, author of Fables and Futures: Biotechnology, Disability, and the Stories We Tell Ourselves.
  • Fall 2019 special double issue of Nine Mile Art & Literary Magazine, including 23-poets in an anthology of Neurodivergent, Disability, Deaf, Mad, and Crip Poetics, edited by Diane R. Wiener.
  • Have Dog, Will Travel: A Poet’s Journey by Stephen Kuusisto, “In a lyrical love letter to guide dogs everywhere, a blind poet shares his delightful story of how a guide dog changed his life and helped him discover a newfound appreciation for travel and independence.”
  • Old Horse, What Is to Be Done? by Stephen Kuusisto, “…Kuusisto is writing at the height of his powers. But what does that mean? It means that the poet finds a lyric key to the word, and knows it. But how is it done, what is his secret? Perhaps it is his knowledge of “the pressure that makes each fact float.” Old Horse, What Is to Be Done? is a beautiful, unrelenting, moving book. It is a book to live with. I love it.” –Ilya Kaminsky, author of Deaf Republic

    Front Cover of "Old Horse, What is to be Done?" by Stephen Kuusisto
    Front Book Cover of “Old Horse, What is to be Done?” by Stephen Kuusisto
  • Wordgathering: A Journal of Disability Poetry and Literature Wordgathering is a digital, Open Access, quarterly journal of disability poetry, literature, and the arts, with two interconnected purposes. First, we are dedicated to providing an accessible venue for featuring the work of emerging and well-known writers with disabilities (disabled writers). Second, we seek to make available and expand a searchable core of this work for interested readers (with and without disabilities) who are committed to disability poetry, literature, and the arts. Wordgathering is hosted as a partnership between the Office of Interdisciplinary Programs and Outreach at the Burton Blatt Institute and Syracuse University Libraries.

Videos/Multimedia

Podcasts

Webinars

Peter Blanck’s commentary about GUDC Universal Design Certification of Grand Rapids Michigan YMCA featured in Architectural Record

April 14, 2016

Most architects would agree that universal design is important. But resources and incentives for creating inclusive environments haven’t always been widely available. To remedy that, the GUDC has developed a universal design certification standard. Based on a decade of research, stakeholder consultation, and testing, the certification standard is scheduled to launch later this year. Continue Reading

Peter Blanck and Universal Design Featured in International Numbers Magazine

April 12, 2016

Universal Architectural Design and People with Disabilities

Universal Design (UD) in the built environment benefits everyone–women and men, older adults and children, people with disabilities and those without, people using different languages. The Global Universal Design Commission (GUDC), along with the architecture and design, development, and disability and aging communities, is accelerating adoption of UD concepts. Continue Reading