Disability, Identity, and the Body as a Context of Choice


Book Description

My dissertation seeks to defend the "mere difference" view of disability from the charge that it leads to objectionable implications in healthcare justice. The mere difference view, briefly put, conceptualizes disability as a morally neutral human trait, analogous to race, sex, gender, ethnicity, and sexual orientation, that ought to be treated in society as such. Its main claim is that disability is not a categorically or definitely bad state to be in but is instead simply another variation of human diversity. Disability as mere difference is a powerful counter to demeaning, pitiable depictions of disabilities as misfortunes and disabled lives as personal tragedies. It is meant to capture and validate the embodied experience and non-tragic identities of disabled people as represented in disability rights and pride movements. For numerous philosophers, this view raises the following worry: if disability were mere difference and not a bad or harmful state to be in, then there apparently would be no moral grounds to support medical research and interventions to prevent, reverse, or remove disability, such as maintaining or restoring the non-disability status of citizens who have become disabled due to some injury or physiological process. This objection is often raised to maintain the bad difference view of disability. In response, I argue that embodiment provides a context of choice that not only makes it possible for us pursue a certain range of life options, but also makes them meaningful in relation to how we understand ourselves and the good life. Abrupt or dramatic changes in a person's embodiment, even though the new embodiment may not be intrinsically or definitely bad, can be inimical to the agency of the modified individual by upending their context of choice. If the state has a responsibility to secure the agency of its citizens and certain physiological states are important conditions for agency--such as providing a stable context of choice--then the state has a moral obligation to secure the physiological conditions for agency through medical interventions. My goal is to provide a plausible account that both contributes to the destigmatization of disability while providing justification for a robust set of entitlements regarding the provision of healthcare resources. In Chapter one, I argue for the mere difference view and elaborate the particular objection that it restricts what medical care and resources citizens are entitled to receive from the state. Chapter two presents the idea that embodiment is an important context of choice for autonomy. Building upon feminist insights on the relation of the body to autonomy and repurposing Will Kymlicka's notion of context of choice, I argue that specific embodied forms not only enable us to pursue a certain range of life options but make them meaningful to us. For this reason, treating or preventing disability through medical interventions may be justified as a practice of identity-maintenance and, in turn, autonomy-maintenance. Chapter three addresses a serious worry that subsidizing healthcare institutions to actively prevent, ameliorate, and eliminate disability expresses a negative social meaning that disability is a devalued embodied form of life, which reinforces the harms of attitudinal and structural ableism. This is an iteration of the expressivist argument that is often deployed in issues of selective reproduction and disability avoidance. I will defend the expressivist argument against prominent objections, recognizing that such devaluations are indeed sometimes expressed. Yet rather than rectifying this social harm by eliminating those practices, I recommend altering the broader social context that imbues disabled life with negative social meaning. This move helps to provide identity and agency maintenance across body types. Chapter four engages with hard cases for my position and offers a justification for providing citizens access to medical resources to alter or augment their bodies in ways that fit with their identity, like gender transition care for transgender people.




The Minority Body


Book Description

Elizabeth Barnes argues compellingly that disability is primarily a social phenomenon—a way of being a minority, a way of facing social oppression, but not a way of being inherently or intrinsically worse off. This is how disability is understood in the Disability Rights and Disability Pride movements; but there is a massive disconnect with the way disability is typically viewed within analytic philosophy. The idea that disability is not inherently bad or sub-optimal is one that many philosophers treat with open skepticism, and sometimes even with scorn. The goal of this book is to articulate and defend a version of the view of disability that is common in the Disability Rights movement. Elizabeth Barnes argues that to be physically disabled is not to have a defective body, but simply to have a minority body.




Exploring Disability Identity and Disability Rights through Narratives


Book Description

Building on David M. Engel and Frank W. Munger’s work analyzing the narratives of people with physical and learning disabilities, this book examines the life stories of twelve physically disabled Canadian adults through the prism of the social model of disablement. Using a grounded theory approach and with extensive reporting of the thoughts of the participants in their own words, the book uses narratives to explore whether an advocacy identity helps or hinders dealings with systemic barriers for disabled people in education, employment, and transportation. The book underscores how both physical and attitudinal barriers by educators, employers and service providers complicate the lives of disabled people. The book places a particular focus on the importance of political economy and the changes to the labour market for understanding the marginalization and oppression of people with disabilities. By melding socio-legal approaches with insights from feminist, critical race, and queer legal theory, Ravi Malhotra and Morgan Rowe ask if we need to reconsider the social model of disablement, and proposes avenues for inclusive legal reform.




Disability, Culture and Identity


Book Description

Disabilities, Culture and Identity is a succinct and accessible presentation of current research on disability, culture and identity. It is an ideal text for students and lecturers alike studying and working in the areas of Disability Studies and Social Policy. Disabilities, Culture and Identity provides a comprehensive and well-structured introduction to an area of growing importance. The authors provide up-to-date and extensive coverage of the development of thinking on cultures of disability, including those relating to people with learning difficulties, people with mental health problems and people with learning difficulties Also covered in detail are critical areas in disability studies including: Development of the social model of disability Disability and the politics of social justice Disability and theories of culture and media Disability, ethnicity and generation The policy options for empowering disabled people, and how the disabled are empowering themselves The disability arts movement Media treatment of disability




Physical Disability and Sexuality


Book Description

This open access edited volume explores physical disability and sexuality in South Africa, drawing on past studies, new research conducted by the editors, and first-person narratives from people with physical disabilities in the country. Sexuality has long been a site of oppression and discrimination for people with disabilities based on myths and misconceptions, and this book explores how these play out for people with physical disabilities in the South African setting. One myth with which the book is centrally concerned, is that people with disabilities are unable to have sex, or are seen as lacking sexuality by society at large. Societal understandings of masculinity, femininity, bodies and attractiveness, often lead people with physical disabilities to be seen as being undesirable romantic or sexual partners. The contributions in this volume explore how these prevailing social conditions impact on the access to sexual and reproductive healthcare, involvement in romantic relationships, childbearing, and sexual citizenship as a whole, of people with physical disabilities in the Western Cape of the country. The authors' research, and first person contributions by people with physical disabilities themselves, suggest that education and public health policy must change, if the sexual and reproductive health rights and full inclusion of people with disabilities are to be achieved.




The Body and Physical Difference


Book Description

Groundbreaking perspectives on disability in culture and the arts that shed light on notions of identity and social marginality




The Oxford Handbook of Philosophy and Disability


Book Description

Disability raises profound and fundamental issues: questions about human embodiment and well-being; dignity, respect, justice and equality; personal and social identity. It raises pressing questions for educational, health, reproductive, and technology policy, and confronts the scope and direction of the human and civil rights movements. Yet it is only recently that disability has become the subject of the sustained and rigorous philosophical inquiry that it deserves. The Oxford Handbook of Philosophy and Disability is the first comprehensive volume on the subject. The volume's contents range from debates over the definition of disability to the challenges posed by disability for justice and dignity; from the relevance of disability for respect, other interpersonal attitudes, and intimate relationships to its significance for health policy, biotechnology, and human enhancement; from the ways that disability scholarship can enrich moral and political philosophy, to the importance of physical and intellectual disabilities for the philosophy of mind and action. The contributions reflect the variety of areas of expertise, intellectual orientations, and personal backgrounds of their authors. Some are founding philosophers of disability; others are promising new scholars; still others are leading philosophers from other areas writing on disability for the first time. Many have disabilities themselves. This volume boldly explores neglected issues, offers fresh perspectives on familiar ones, and ultimately expands philosophy's boundaries. More than merely presenting an overview of existing work, this Handbook will chart the growth and direction of a vital and burgeoning field for years to come.




Disability, Media, and Representations


Book Description

Bringing together scholars from around the world to research the intersection between media and disability, this edited collection aims to offer an interdisciplinary exploration and critique of print, broadcast and online representations of physical and mental impairments. Drawing on a wide range of case studies addressing how people can be ‘othered’ in contemporary media, the chapters focus on analyses of hateful discourses about disability on Reddit, news coverage of disability and education, media access of individuals with disabilities, the logic of memes and brain tumour on Twitter, celebrity and Down Syndrome on Instagram, disability in TV drama, the metaphor of disability for the nation; as well as an autoethnography of treatment of breast cancer. Providing a much-needed global perspective, Disability, Media, and Representations examines the relationship between self-representation and representations in either reinforcing or debunking myths around disability, and ways in which academic discourse can be differently articulated to study the relationship between media and disability. This book will be of interest to students and researchers of disability studies and media studies as well as activists and readers engaged in debates on diversity, inclusivity and the media.




Disability Visibility


Book Description

“Disability rights activist Alice Wong brings tough conversations to the forefront of society with this anthology. It sheds light on the experience of life as an individual with disabilities, as told by none other than authors with these life experiences. It's an eye-opening collection that readers will revisit time and time again.” —Chicago Tribune One in five people in the United States lives with a disability. Some disabilities are visible, others less apparent—but all are underrepresented in media and popular culture. Activist Alice Wong brings together this urgent, galvanizing collection of contemporary essays by disabled people, just in time for the thirtieth anniversary of the Americans with Disabilities Act, From Harriet McBryde Johnson’s account of her debate with Peter Singer over her own personhood to original pieces by authors like Keah Brown and Haben Girma; from blog posts, manifestos, and eulogies to Congressional testimonies, and beyond: this anthology gives a glimpse into the rich complexity of the disabled experience, highlighting the passions, talents, and everyday lives of this community. It invites readers to question their own understandings. It celebrates and documents disability culture in the now. It looks to the future and the past with hope and love.




The Sexual Politics of Disability


Book Description

While the civil rights movement has put disability issues centre-stage, there has been minimal discussion of disabled people's sexuality. This book, based on first-hand accounts, takes a close look at questions of identity, relationships, sex, love, parenting and abuse and demolishes the taboo around disability and sex. It shows the barriers to disabled people's sexual rights and sexual expression, and also the ways in which these obstacles are being challenged. Variously moving, angry, funny and proud, The Sexual Politics of Disability is about disabled people sharing their stories and claiming their place as sexual beings. It is a pioneering work, and essential reading for anyone interested in disability or sexual politics.