Disability Memoir

A searing debut YA poetry and essay collection about a Black cancer patient who faces medical racism after being diagnosed with leukemia in their early twenties, for fans of Audre Lorde's The Cancer Journals and Laurie Halse Anderson's Shout. When Walela is diagnosed at twenty-three with...

What would you have left if you awoke and were told you would be paralyzed from the eyes down for the rest of your life? After an almost fatal car crash and a botched surgery to repair nerve damage, that was Clay Byars' reality at 18 years old. Determination became the only constant in his life from that point on, and miraculously he quickly began to defy the odds. Clay discovered a life far different from that of his identical twin brother, Will.

A hopeful look at coping with the ravages of serious chronic illness by an accomplished journalist, a contributing columnist for the New York Times, and former senior producer of the CBS Evening News Richard Cohen, a veteran journalist, has lived with multiple sclerosis for 30 years. Diagnosed...

Jan Grue was diagnosed with spinal muscular atrophy at the age of three. Shifting between specific periods of his life - his youth with his parents and sister in Norway; his years of study in Berkeley, St. Petersburg, and Amsterdam; and his current life as a professor, husband, and father - he intersperses these histories with elegant, astonishingly wise reflections on the world, social structures, disability, loss, relationships, and the body: in short, on what it means to be human.

En este libro de memorias profundamente conmovedor y sincero, Blanca Reyes Méndez comparte su viaje tras la pérdida repentina e irreversible de la visión de su ojo izquierdo. A través de la reflexión poética y la verdad personal, explora el dolor, el miedo, la curación y la transformación. Ver con el alma no trata sólo de la pérdida de visión, sino de aprender a ver de otra manera. A encontrar la luz interior. A vivir más despacio, más plenamente y con el corazón bien abierto.

In Laughing and Crying Alone, we are offered a compelling account of the struggles associated with bipolar disorder. Alternately heartbreaking and uplifting, we follow Lisa through the laughter and the tears. Exploring Lisa's feelings of isolation, Laughing and Crying Alone provides compassion and validation to those with mental illness while shedding a much-needed light on mental health. And through it all, we see a wife and mother come to terms with the uncertainties of living with bipolar disorder and reemerge to embrace the new normal with confidence and ease.

A collision with a moose on a dark highway left Susan Mockler with an incomplete spinal injury, suddenly compromising her ability to walk and to care for herself. She spent months in a rehabilitation facility learning how to adjust to her new reality, and though her body partially recovered, every aspect of her life changed.

"If you can dream it, you can do it!" - das ist bei Oliver Brünner keine Floskel. Dabei sah im Leben des heute erfolgreichen Speakers eigentlich alles ganz anders aus. Noch während seiner Geburt zieht sich die Nabelschnur seiner Mutter wie eine Schlinge um seinen Hals, weswegen er fortan mit einer spastischen Tetraparese lebt. Doch Oliver trotzt den vermeintlichen Widrigkeiten und kann heute auf einen Lebensweg zurückblicken, den dem schon früh als "Sorgenkind" titulierten Jungen wohl niemand zugetraut hätte. Seine Geheimwaffe: das Träumen.

This program is read by the author. An inspiring memoir of a young man who discovered he was going completely deaf just at the moment he’d fallen in love for the first time. As a child, Matt Hay didn’t know his hearing wasn’t the way everyone else processed sound—because of the...

There Are No Answers Here, Only Questions is the true story of two life-altering events and the personal transformation that resulted from their unlikely collision. It's the story of an owner preparing to sell his business and retire just as he is diagnosed with cancer.

Featured in The Advocate, New York Times, Literary Hub, Autostraddle, and New York magazine's The Cut This is a vital exploration of the ways society overlooks—and fails—young women with disabilities and chronic illnesses Miriam’s doctor didn’t believe she had breast cancer. She did...

Driven by the pursuit of perfection and the desire to truly be loved and accepted, Cynthia battled an eating disorder for thirteen long years. “Starving, Bingeing, Purging” is her raw, authentic story, told firsthand; a story not just of suffering, but of resilience, victory, and hope against all odds. In this book, Cynthia openly explores the complex issues of anorexia, bulimia, purging, and food addiction, and shares the intimate details of her journey to reclaim her life.

Le destin de Simone s’est écrit le jour de sa naissance. Son premier cri, elle le pousse en partie à cause d’un arrachement du plexus brachial qui paralyse son bras droit. Comme dans 80 % des situations, son handicap est invisible. Pourtant, à force de volonté et de courage elle embrasse une carrière de handballeuse, jusqu’à atteindre le très haut niveau.

In 1963, Philip Hodges was born, the seventh of eight children, inflicted with Cerebral Palsy. Thanks to the loving devotion of their parents, who saw Philip as a gift and not a burden, the author and his siblings experienced the power of love, devotion, and acceptance that forever changed their lives.

In 1959, the year Terry Galloway turned nine, the voices of everyone she loved began to disappear. No one yet knew that an experimental antibiotic given to her mother had wreaked havoc on her fetal nervous system, eventually causing her to go deaf. As a self-proclaimed "child freak," she acted out her fury with her boxy hearing aids and Coke-bottle glasses by faking her own drowning at a camp for crippled children

Tara Sidhoo Fraser is thirty-one years old when a rare mutation in her brain causes a stroke. Awakening after surgery with no memory of her previous life, she attempts to piece it all back together through a haze of amnesia. Yet, as memories do begin to surface, they are seen through someone else's eyes—the person whose body she stole, whom she calls Ghost.

Ruth's tribe are her lively children and her filmmaker husband, Simon, who has motor neurone disease and can communicate only with his eyes. Ruth's other tribe are the friends who gather at the cove in Greystones, Co. Wicklow, and regularly throw themselves into the freezing cold water just for kicks. The Tragic Wives' Swimming Club, as they jokingly call themselves, meet to cope with the extreme challenges life puts in their way, not to mention the monster waves rolling over the horizon.

Helen Keller’s name is forever linked with courage, perseverance, and the power of education. In Midstream: My Later Life, she picks up where The Story of My Life left off, offering a rare look at her journey beyond her early triumphs. Here, Keller recounts the challenges and victories of adulthood—her advocacy for people with disabilities, her international travels, her friendships with world leaders and artists, and her tireless fight for social change. She writes candidly about setbacks, loneliness, and the weight of public life, but also about the deep sense of purpose that guided her.

Damiano e Margherita sono due fratelli che hanno molte cose in comune: la voglia di mettersi in gioco, la caparbietà e la tenacia nel voler inseguire i propri sogni, e l'autismo. Insieme si sono esibiti in televisione e, mano nella mano sul palcoscenico, sembrano finalmente aver trovato il loro posto nel mondo. Già dalla mattina successiva, però, i due sono obbligati a tornare alla realtà. Damiano vive a Rimini e ha le idee molto chiare sul futuro: una moglie – "l'altra metà della mela" – con cui avere dai dodici ai venti figli, milioni di dischi venduti, concerti in tutto il mondo.

In 1959, at the age of 21, Max Starkloff was in a car accident that left him paralyzed from the neck down. His doctors doubted he would live longer than a few days, and, if he survived, the hope for his quality of life would be minimal. How did this young man with barely a high school education become the leader of a powerful disability rights movement and the founder of the Starkloff Disability Institute? This is his remarkable story.