Disability Biography

Lauren Windas is one of the estimated 250,000 people suffering with CFS in the UK. Whilst at university in 2012, she fell ill with a viral infection and was later diagnosed with CFS. Since then she has devoted herself to reclaiming her health and being able to live a full life, drawing on the knowledge of experts to help manage her often mysterious and hard-to-manage condition. In Chronic Fatigue Syndrome, Lauren recounts the highs and lows of her own health journey and experiences,.

NEW YORK TIMES BESTSELLER This essay collection from the “bitches gotta eat” blogger, writer on Hulu’s Shrill and HBO's And Just Like That, and “one of our country’s most fierce and foulmouthed authors” (Amber Tamblyn, Vulture) is sure to make you alternately cackle with glee and...

The incredible life story of Haben Girma, the first Deafblind graduate of Harvard Law School, and her amazing journey from isolation to the world stage. Haben grew up spending summers with her family in the enchanting Eritrean city of Asmara. There, she discovered courage as she faced off...

Jason Dunkerley’s Visions of Hope: Running Towards My Own Truth is the inspiring autobiography of a distinguished Canadian middle-distance runner, who has been blind from birth due to a congenital eye condition. He achieved international acclaim as a five-time Paralympic medalist and world champion.

Tony-award winning actress Ali Stroker reads the story of Judy Heumann—one of the most influential disability rights activists in US history A story of fighting to belong in a world that wasn’t built for all of us and of one woman’s activism—from the streets of Brooklyn and San Francisco...

In Fractured Realities, Ryder Budden shares a deeply personal and raw account of his life with schizophrenia, offering a rare glimpse into the struggle, resilience, and hope that defines his journey. From vivid hallucinations and delusional paranoia to the gradual path toward healing, this memoir explores the highs and lows of navigating a fractured reality. Ryder's story begins with childhood encounters with the impossible, from seeing extra limbs in reflections to vivid visions of God.

John Cotter was thirty years old when he first began to notice a ringing in his ears. Soon the ringing became a roar inside his head. Next came partial deafness, then dizziness and vertigo that rendered him unable to walk, work, sleep, or even communicate. At a stage of life when he expected to be emerging fully into adulthood, teaching, and writing books, he found himself “crippled and dependent” and in search of care.

In Take Me Home from the Oscars, Schwab tells for the first time her story of living an amazing life in television while suffering from rheumatoid arthritis. Schwab recounts with incredible honesty how on the same day she produced and appeared in a major makeover segment for Live with Regis & Kelly in New York and then raced to Chicago to appear on Oprah!, all while balancing medications to ward off the relentless pain that plagued her on-camera and off.

Until sophomore year of high school, 15-year-old Allison Britz lived a comfortable life in an idyllic town. She was a dedicated student with tons of extracurricular activities, friends, and loving parents at home. But after awakening from a vivid nightmare in which she was diagnosed with brain cancer, she was convinced the dream had been a warning. Allison believed that she must do something to stop the cancer in her dream from becoming a reality.

A New York Times Book Review Editors' Choice Kate Bowler's The Everything Happens Book Club Pick! Award-winning writer Heather Lanier's memoir about raising a child with a rare syndrome, defying the tyranny of normal, and embracing parenthood as a spiritual practice that breaks us open in...

Known and loved by his family and friends as quirky and different, Travis is a man on a mission to find his purpose in a world that often throws him grenades. Through the pitfalls of high school, the workplace and dating scene, he shares an honest account of his personal struggles with undiagnosed autism, ADHD and dyslexia. Written with dark humour and powerful reflection, Stairway to the Spectrum is an entertaining and thought-provoking memoir which will appeal to anybody who has ever felt uncomfortable in their own skin.

Fairy tales shape how we see the world, so what happens when you identify more with the Beast than Beauty? Amanda Leduc looks at fairy tales from the Brothers Grimm to Disney, showing us how they influence our expectations and behaviour and linking the quest for disability rights to new kinds of stories that celebrate difference.

FINALIST FOR THE PULITZER PRIZE Named one of the best books of the year by: THE NEW YORKER THE WASHINGTON POST THE ATLANTIC NPR PUBLISHERS WEEKLY LITHUB "Fascinating...The great strength of this memoir is its voracious, humble curiosity." - The Atlantic, The 10 Best Books...

In The Maniac with No Knees, Tyler Kania takes listeners on a raw, unfiltered ride through his journey with undiagnosed Bipolar I Disorder. From rugby fields to the edge of the Grand Canyon, from building a cryptocurrency start-up to coaching a women’s rugby team to victory, Tyler’s manic adventures push every boundary. Along the way, he uncovers a major tech scandal, survives run-ins with the Boston Mafia, and even attempts the unthinkable—before landing in a mental hospital, where he finally begins to heal.

“Honey, you’ve been very ill and they’ve had to amputate…” His voice cracked. I searched his face, looking for some kind of clue to tell me why I sensed so much pain from him and in me. “…Your hands and feet.” Cyndi tried to grasp the new reality that flesh-eating disease had changed her life forever. Her recent memories of being a successful business manager and new mom seemed oceans away. It just couldn’t be true. I tried to speak, but no words came. Please God—let this be a dream.

The long-awaited essay collection from one of the most influential voices in disability activism that detonates a bomb in our collective understanding of care and illness, showing us that sickness is a fact of life. In the wake of the 2014 Ferguson riots, and sick with a chronic condition that...

Trente-deux ans, c'est le nombre d'années qu'il m'a fallu pour mettre un nom sur ma différence. Comment ai-je pu "passer au travers des mailles du filet" durant tout ce temps ? Je vous révèle, au travers de ce récit parsemé d'anecdotes, comment j'ai grandi dans l'ignorance de mon syndrome. Plongez dans mon quotidien et découvrez chacune des étapes clés de mon évolution ainsi que les moyens mis en œuvre pour survivre dans ce monde parfois difficile à appréhender.

One misstep on a mountain climbing trip plunged Brenden into darkness by stealing his sight—and everything else he held dear. But an independent guide dog named Nelson might just bring him back to life . . . if they don't kick him out of guide dog school first. Twenty-two-year-old Brenden...

The first book to cover the entirety of disability history, from pre-1492 to the present Disability is not only the story of someone we love or the story of whom we may become; rather it is undoubtedly the story of our nation. Covering the entirety of US history from pre-1492 to the present, A...

He Called Me Tin is a story of triumph and perseverance. From childhood distress to an attempt at suicide to being scarred by religion to being diagnosed with multiple sclerosis to the strife of racism and discrimination as a government employee to being assaulted and nearly kidnapped abroad, she has overcome in peace....