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VIRTUAL READS @ UNIVERSITY LIBRARIES
Becoming Citizens by
Following the Second World War, a generation of Seattle parents went against conventional medical wisdom and chose to bring up their children with developmental disabilities in the community. This book presents a stunning visual narrative of thirteen of these remarkable families. With a rich array of interviews, photographs, newspaper clippings, official documents, and personal mementos, photographer Susan Schwartzenberg captures moving recollections of the struggle and perseverance of these parents. Becoming Citizens traces their dogged determination to make meaningful lives for their children in the face of an often hostile system. Breaking the silence that characterizes the history of disability in the United States, Becoming Citizens is a substantive contribution to social and regional history. It demonstrates the ways in which personal experiences can galvanize communities for political action. The centerpiece of the book is the story of four mothers-turned-activists who coauthored Education for All, a crucial piece of Washington State legislation that was a precursor to the national law securing educational rights for every person with a disability in America. Becoming Citizens is a deeply compassionate testament to the experience of family life and disability, as it is to the ways in which ordinary citizens become activists. It will be important to anyone interested in disability studies, including teachers, friends, and families of those with disabilities.
ISBN: 9780295806914Publication Date: 2016-06-01
Disability and Mothering by
Editors Lewiecki-Wilson and Cellio have put together the first book to focus on the intersecting spaces, both cultural and personal, of disability and mothering. Derived from the Latin for threshold, the word "liminal" calls attention to the book's focus on the transitional moments and spaces where the personal and social, inside and outside, self and other converge. The volume features twenty-one previously unpublished essays by new as well as established scholars and community activists. Contributors, some of whom are themselves disabled or mothers of children with disabilities, present moving personal accounts and accessible scholarship grounded in historical study, experiential and retrospective analysis, interviews, social research, and feminist and disability studies theories. In their introduction, the editors survey the theoretical frameworks of feminism and disability studies, locating the points of overlap crucial to a study of disability and mothering. Organized in five sections, the book engages questions about reproductive technologies; diagnoses and cultural scripts; the ability to rewrite narratives of mothering and disability; political activism; and the tensions formed by the overlapping identities of race, class, nation, and disability. The essays speak to a broad audience--from undergraduate and graduate students in women's studies and disability studies, to therapeutic and health care professionals, to anyone grappling with issues such as genetic testing and counseling, raising a child with a disability, or being disabled and contemplating starting a family.
ISBN: 9780815650805Publication Date: 2011-01-01
Metanarratives of Disability by
This book explores multiple metanarratives of disability to introduce and investigate the critical concept of assumed authority and the normative social order from which it derives. The book comprises 15 chapters developed across three parts and, informed by disability studies, is authored by those with research interests in the condition on which they focus as well as direct or intimate experiential knowledge. When out and about, many disabled people know only too well what it is to be erroneously told the error of our/their ways by non-disabled passers-by, assumed authority often cloaked in helpfulness. Showing that assumed authority is underpinned by a displacement of personal narratives in favour of overarching metanarratives of disability that find currency in a diverse multiplicity of cultural representations - ranging from literature to film, television, advertising, social media, comics, art, and music - this work discusses how this relates to a range of disabilities and chronic conditions, including blindness, autism, Down syndrome, diabetes, cancer, and HIV and AIDS. Metanarratives of Disability will be of interest to all scholars and students of disability studies, medical sociology, medical humanities, education studies, cultural studies, and health. 'offers a well-structured, accessible collection of disability narratives that foreground disabled voices' Journal of Literary and Cultural Disability Studies 16.1 (2022)
ISBN: 9781003057437Publication Date: 2021-05-26
Recovering Bodies by
This is a provocative look at writing by and about people with illness or disability--in particular HIV/AIDS, breast cancer, deafness, and paralysis--who challenge the stigmas attached to their conditions by telling their lives in their own ways and on their own terms. Discussing memoirs, diaries, collaborative narratives, photo documentaries, essays, and other forms of life writing, G. Thomas Couser shows that these books are not primarily records of medical conditions; they are a means for individuals to recover their bodies (or those of loved ones) from marginalization and impersonal medical discourse. Responding to the recent growth of illness and disability narratives in the United States--such works as Juliet Wittman's Breast Cancer Journal, John Hockenberry's Moving Violations, Paul Monette's Borrowed Time: An AIDS Memoir, and Lou Ann Walker's A Loss for Words: The Story of Deafness in a Family--Couser addresses questions of both poetics and politics. He examines why and under what circumstances individuals choose to write about illness or disability; what role plot plays in such narratives; how and whether closure is achieved; who assumes the prerogative of narration; which conditions are most often represented; and which literary conventions lend themselves to representing particular conditions. By tracing the development of new subgenres of personal narrative in our time, this book explores how explicit consideration of illness and disability has enriched the repertoire of life writing. In addition, Couser's discussion of medical discourse joins the current debate about whether the biomedical model is entirely conducive to humane care for ill and disabled people. With its sympathetic critique of the testimony of those most affected by these conditions, Recovering Bodies contributes to an understanding of the relations among bodily dysfunction, cultural conventions, and identity in contemporary America.
ISBN: 9780299155636Publication Date: 1997-11-01
Sexy Like Us by
Sexy Like Us: Disability, Humor, and Sexuality takes a humorous, intimate approach to disability through the stories, jokes, performances, and other creative expressions of people with disabilities. Author Teresa Milbrodt explores why individuals can laugh at their leglessness, find stoma bags sexual, discover intimacy in scars, and flaunt their fragility in ways both hilarious and serious. Their creative and comic acts crash, collide, and collaborate with perceptions of disability in literature and dominant culture, allowing people with disabilities to shape political disability identity and disability pride, call attention to social inequalities, and poke back at ableist cultural norms. This book also discusses how the ambivalent nature of comedy has led to debates within disability communities about when it is acceptable to joke, who has permission to joke, and which jokes should be used inside and outside a community's inner circle. Joking may be difficult when considering aspects of disability that involve physical or emotional pain and struggles to adapt to new forms of embodiment. At the same time, people with disabilities can use humor to expand the definitions of disability and sexuality. They can help others with disabilities assert themselves as sexy and sexual. And they can question social norms and stigmas around bodies in ways that open up journeys of being, not just for individuals who consider themselves disabled, but for all people.
ISBN: 9781496838964Publication Date: 2022-07-27
The Stigma of Disease and Disability by
People with physical or mental disabilities such as HIV, substance abuse, cancer, or depression are negatively affected not only by the disease, but also by others' negative reactions to it. This humane book prepares advocates and health care professionals to more effectively fight the social injustice of stigma and better support the families of those with disabilities. Readers will gain a solid understanding of the common experience of stigma as well as how to combat prejudiced responses to specific disabilities, including childhood disorders, obesity, and Alzheimer's disease.
ISBN: 9781433815836Publication Date: 2013-12-15
Such a Pretty Girl : a Story of Struggle, Empowerment, and Disability Pride by
Such a Pretty Girl is Nadina LaSpina's story--from her early years in her native Sicily, where still a baby she contracts polio, a fact that makes her the object of well-meaning pity and the target of messages of hopelessness; to her adolescence and youth in America, spent almost entirely in hospitals, where she is tortured in the quest for a cure and made to feel that her body no longer belongs to her; to her rebellion and her activism in the disability rights movement. LaSpina's personal growth parallels the movement's political development--from coming together, organizing, and fighting against exclusion from public and social life, to the forging of a common identity, the blossoming of disability arts and culture, and the embracing of disability pride. While unique, the author's journey is also one with which many disabled people can identify. It is the journey to find one's place in an ableist world--a world not made for disabled people, where disability is only seen in negative terms. La Spina refutes all stereotypical narratives of disability. Through the telling of her life's story, without editorializing, she shows the harm that the overwhelming focus on pity and on a cure that remains elusive has done to disabled people. Her story exposes the disability prejudice ingrained in our sociopolitical system and denounces the oppressive standards of normalcy in a society that devalues those who are different and denies them basic rights. Written as continuous narrative and in a subtle and intimate voice, Such a Pretty Girl is a memoir as captivating as a novel. It is one of the few disability memoirs to focus on activism, and one of the first by an immigrant.
ISBN: 9781613321058Publication Date: 2019
Surface Tensions by
Surface Tensions is an expansive, yet intimate study of how people remake themselves after catastrophic bodily changeOCothe loss of limbs, the loss of function, the loss or replacement of organs. Against a sweeping cultural backdrop of art, popular culture, and the history of science and medicine, Manderson uses narrative epistemology based on in-depth interviews with over 300 individuals to show how they re-establish the coherence of their bodies, identities, and biographies. In addition to offering important new insights into the care, rehabilitation, and rehabituation of post-trauma patients, MandersonOCOs work challenges conventional ideas about the nature of embodiment and is an important contribution to medical anthropology, disability studies, and cultural studies.
ISBN: 9781611320992Publication Date: 2011-10-01
Uncanny bodies : superhero comics and disability by
Superhero comics reckon with issues of corporeal control. And while they commonly deal in characters of exceptional or superhuman ability, they have also shown an increasing attention and sensitivity to diverse forms of disability, both physical and cognitive. The essays in this collection reveal how the superhero genre, in fusing fantasy with realism, provides a visual forum for engaging with issues of disability and intersectional identity (race, ethnicity, class, gender, and sexuality) and helps to imagine different ways of being in the world. Working from the premise that the theoretical mode of the uncanny, with its interest in what is simultaneously known and unknown, ordinary and extraordinary, opens new ways to think about categories and markers of identity, Uncanny Bodies explores how continuums of ability in superhero comics can reflect, resist, or reevaluate broader cultural conceptions about disability. The chapters focus on lesser-known characters--such as Echo, Omega the Unknown, and the Silver Scorpion--as well as the famous Barbara Gordon and the protagonist of the acclaimed series Hawkeye, whose superheroic uncanniness provides a counterpoint to constructs of normalcy. Several essays explore how superhero comics can provide a vocabulary and discourse for conceptualizing disability more broadly. Thoughtful and challenging, this eye-opening examination of superhero comics breaks new ground in disability studies and scholarship in popular culture.
ISBN: 9780271086309Publication Date: 2019
Why I Burned My Book by
This wide-ranging book shows why Paul Longmore is one of the most respected figures in disability studies today. Understanding disability as a major variety of human experience, he urges us to establish it as a category of social, political, and historical analysis in much the same way that race, gender, and class already have been. The essays here search for the often hidden pattern of systemic prejudice and probe into the institutionalized discrimination that affects the one in five Americans with disabilities.Whether writing about the social critic Randolph Bourne, contemporary political activists, or media representations of people with disabilities, Longmore demonstrates that the search for heroes is a key part of the continuing struggle of disabled people to gain a voice and to shape their destinies. His essays on bioethics and public policy examine the conflict of agendas between disability rights activists and non-disabled policy makers, healthcare professionals, euthanasia advocates, and corporate medical bureaucracies. The title essay, which concludes the book, demonstrates the necessity of activism for any disabled person who wants access to the American dream.
ISBN: 9781592137756Publication Date: 2009-08-21
To search for other titles in the ebook format:
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STREAMING VIDEOS
What does it mean to be disabled and how does it shape an artist's work? This documentary explores what is known as the disability art movement, following five artists-including a painter, a writer, an actor, a theater director, and a filmmaker, all of whom happen to have physical disabilities-through their creative work. Intense group discussions of artistic and personal goals are also recorded. Dispelling the myth of tragic disability, the film depicts its subjects as, first and foremost, creative people. The result is a profound look at, and celebration of, the act of making art-viewed through the lens of disability and the rejection of its stereotypes
Young, disabled, and famous / produced and directed by Nina Beveridge
Renee doesn't want to make you cry. And she doesn't want your pity. In this fly-on-the-wall view of 21 year old author, internet star, and muscular dystrophy sufferer Renee Rodriguez, her wit and no-nonsense attitude shine through.
A selection of feature films from well-known studios such as MGM, Miramax, United Artists, Columbia Pictures, and Dreamworks.
PODCASTS
Welcome to POWER NOT PITY, where we explore the lives of disabled people of color everywhere! Through storytelling, commentary and analysis, the podcast aims to amplify the lived experiences and perspectives of disabled people.
In an effort to break down the systemic barriers that keep disabled people of color silenced, this show serves as a vehicle to dismantle ableism with grace, humor and downright determination.
So... “What’s your disabled power?”
Uniquely Human: the Podcast expands the conversation on autism and neurodiversity by amplifying the voices of autistic individuals and thought leaders in providing insightful, cutting-edge and practical information about the autistic experience. Hosted by Barry Prizant and Dave Finch.
A less-than-inspiring exploration of disability from someone who is actually disabled. Heavy on the sarcasm, Bad Attitudes explores the reality of being disabled, how non-disabled people can become better advocates and allies, disability representation in pop culture, and the ways in which disability permeates society. Young or sensitive ears beware. N (always) SFW.
20 Best Disability Podcasts
Please Note: The podcasts listed are not resources held by the University Libraries. There is no guarantee that the resources will be available or accessible to all users. Nor does the University Libraries endorse any views expressed during the podcasts.
AUDIOBOOKS!
Listen to the following audiobooks:
Pain and shock in America : politics, advocacy, and the controversial treatment of people with disabilities by
For more than forty years, professionals in the field of disability studies have engaged in debates over the use of aversive interventions (such as electric shock) like the ones used at the Judge Rotenberg Center. Advocates and lawyers have filed complaints and lawsuits to both use them and ban them, scientists have written hundreds of articles for and against them, and people with disabilities have lost their lives and, some would say, lived their lives because of them. All of these families have children who have been excluded from numerous educational and treatment programs because of their behaviors. For most of the families, placement at the Judge Rotenberg Center is the last resort. This book is a historical case study of the Judge Rotenberg Center, named after the judge who ruled in favor of keeping its doors open to use aversive interventions. It chronicles and analyzes the events and people involved for over forty years that contributed to the inability of the state of Massachusetts to stop the use of electric shock, and other severe forms of punishment on children and adults with disabilities. It is a long story, sad and tragic, complex, filled with intrigue and questions about society and its ability to protect and support its most vulnerable citizens
ISBN: 9781666173581Publication Date: 2021
The Curse of Chalion by
Amidst the decaying splendor and poisonous intrigue of Chalion s ancient capital, Lord Cazaril is forced to confront not only powerful enemies but also the malignant curse that clings to the royal household, trapping him, flesh and soul, in a maze of demonic paradox, damnation, and death for as long as he dares walk the five-fold pathway of the gods.
ISBN: 9780786132348Publication Date: 2007-01-01
To search for other titles in the audiobook format:
- Go to the Library Catalog
- Type search terms/title/author in the search box
- Limit the Format to Streaming Audio
- Click the search icon
- View the list of titles and make your selection!
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