Category: Non-Fiction
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‘Surviving and Thriving with an Invisible Chronic Illness’- Jacqueline, Ilana
“An important antidote to the dogmatic ‘kale and vitamins’ tone of most ‘self-help’ literature.” —Alexa Tsoulis-Reay, senior writer, New York magazine Popular blogger Ilana Jacqueline offers smart and savvy advice, humor, and practical tips for living with an invisible chronic illness. Do you live with a chronic, debilitating, yet invisible condition? You may feel isolated,…
The Disability Archives
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‘Sounds Like Home’- Wright, Mary Herring
Mary Herring Wright’s memoir adds an important dimension to the current literature in that it is a story by and about an African American deaf child. The author recounts her experiences growing up as a deaf person in Iron Mine, North Carolina, from the 1920s through the 1940s. Her story is unique and historically significant…
The Disability Archives
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‘Sitting Pretty’- Taussig, Rebekah
A memoir-in-essays from disability advocate and creator of the Instagram account @sitting_pretty Rebekah Taussig, processing a lifetime of memories to paint a beautiful, nuanced portrait of a body that looks and moves differently than most. Growing up as a paralyzed girl during the 90s and early 2000s, Rebekah Taussig only saw disability depicted as something…
The Disability Archives
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‘The Right to Maim’- Puar, Jasbir K.
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…
The Disability Archives
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‘QDA: A Queer Disabled Anthology’- Luczak, Raymond
Featuring fiction, poetry, nonfiction, and comics by 48 writers from around the world, QDA: A Queer Disability Anthology proves that intersectionality isn’t just a buzzword. It’s a penetrating and unforgettable look into the hearts and souls of those defiant enough to explore their own vulnerabilities and demonstrate their own strengths. “Queer sexuality and disability places…
The Disability Archives
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‘Physical Disability in British Romantic Literature’- Joshua, Essaka
The modern concept of disability did not exist in the Romantic period. This study addresses the anachronistic use of ‘disability’ in scholarship of the Romantic era, providing a disability studies theorized account that explores the relationship between ideas of function and aesthetics. Unpacking the politics of ability, the book reveals the centrality of capacity and…
The Disability Archives
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‘The Pedagogy of Pathologization’- Annamma, Subini Ancy
Linking powerful first-person narratives with structural analysis, The Pedagogy of Pathologization explores the construction of criminal identities in schools via the intersections of race, disability, and gender. amid the prevalence of targeted mass incarceration. Focusing uniquely on the pathologization of female students of color, whose voices are frequently engulfed by labels of deviance and disability,…
The Disability Archives
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‘Nothing About Us Without Us’- Charlton, James I
James Charlton has produced a ringing indictment of disability oppression, which, he says, is rooted in degradation, dependency, and powerlessness and is experienced in some form by five hundred million persons throughout the world who have physical, sensory, cognitive, or developmental disabilities. Nothing About Us Without Us is the first book in the literature on…
The Disability Archives
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‘No Right to Be Idle’- Rose, Sarah F.
During the late nineteenth and early twentieth centuries, Americans with all sorts of disabilities came to be labeled as “unproductive citizens.” Before that, disabled people had contributed as they were able in homes, on farms, and in the wage labor market, reflecting the fact that Americans had long viewed productivity as a spectrum that varied…
The Disability Archives
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‘My Body and Other Crumbling Empires’- Medford, Lyndsey
We are living in a world that is sick. Both literally sick, with 60 percent of adults in the US living with a chronic illness and rising rates of autoimmune diseases in particular, including long COVID, and figuratively sick, facing ever increasing rates of burnout, anxiety, and disconnection. As a writer, activist, and theology student,…
The Disability Archives
