Showing titles in People with Disabilities

In November 1991, author Eugen Ehrenberg was diagnosed with multiple sclerosis, and he learned how to manage the imminent limitations in his movements. Twenty years after that, he suffered an accident that left him in the hospital for a long time as he managed to regain part of his mobility. He had to become friendly with his new active wheelchair and later with his hand bike.

The Moment Everything Changed is what makes this book different—it’s not clinical, it’s personal and confrontational. I remember the exact moment I opened my eyes and something was different. Not a little different, everything different. Three decades of pain, illness, disease that created constant noise in my body, mind, and soul to opening my eyes after surgery #21… POOF!!! It was gone. Just gone! Nobody prepares you for that. We spend so much time asking, “Why am I in pain & will it ever stop?” “Why can’t anyone figure it out and just help me?” Tough times...

What does it mean to think differently in a world that wasn't built for your mind? Jake Didinsky is autistic, queer, non-binary, and Jewish. They've spent their life building an operating system to survive—a framework for navigating ethics, systems, and human connection when the default settings keep crashing. The Architecture of Uncertainty is part memoir, part philosophy, and entirely honest.

A NEW YORKER BEST BOOK OF THE YEAR A poignant memoir of love, trauma, and recovery after a life-changing stroke, twinned to a powerful account of his father's experience in World War II, by a winner of the National Book Critics Circle Award. “A beautiful, compelling memoir...Raban’s...

It was August 25, 2006, my first on-camera studio open for the CBS News broadcast 60 Minutes. Executive Producer Jeff Fager poked his head in the dressing room." Good luck, Brotha! You've come a long way to get here. You've earned it." …If only he knew. My mind flashed back to elementary...

In the fall of 1988, Sue Miller found herself caring for her father as he slipped into the grasp of Alzheimer's disease. She was, she claims, perhaps the least constitutionally suited of all her siblings to be in the role in which she suddenly found herself, and in The Story of My Father she...

#1 International Bestseller When Owen met Haatchi, the lives of one adorable little boy and one great, big dog were destined to change forever. Owen-known to his family as "little buddy" or "Little B"-has a rare genetic disorder that leaves him largely confined to a wheelchair. Before being...

Acclaimed Friday Night Lights author Buzz Bissinger shares the moving and uplifting tale of his cross-country journey with his adult savant son who suffered brain damage at birth. Buzz Bissinger’s twin sons were born three minutes—and a world—apart. Gerry, the older one, is a graduate...

A riveting and candid account of a young journalist's awakening to a life of chronic illness, weaving together her personal story with reporting to shed light on how Americans live with long-term diagnoses today. Tessa Miller was an ambitious twentysomething writer in New York City when, on a...

Liz Casper is a former medical doctor, artist, and author from the Pacific Northwest. In her first book, BRILLIANT, BEAUTIFUL, BIPOLAR, Liz shares with us her personal journey before, during, and after her diagnosis of bipolar disorder. The book, set in Los Angeles and Las Vegas, chronicles Liz’s experience both living with and healing from this devastating diagnosis.

Beyond the nerve is a raw and unfiltered journey through five years of living with pudenda neuralgia—a condition that tested every ounce of my resilience while reshaping my purpose. It delves into the struggles and triumphs of managing chronic pain, the emotional toll of invisible battles, and the lessons learned in advocating for myself when support wasn't always easy to find.

For fans of rags-to-riches stories, Be There When I Return is not just about overcoming epilepsy and finding success—it is also for those who are looking for a celebration of love in its purest form. When thirty-one-year-old Michael starts to act out of character, it gets the attention of his roommate and a woman he has started dating. After denying anything is wrong with him, Michael finally decides to visit a neurologist. His life takes an unexpected turn when he receives a life-altering diagnosis of epilepsy.

This true love story follows Lars and Amanda, two twenty-somethings who fall deeply in love, with big plans for their future together, only to have the rug pulled out from beneath them when Lars is diagnosed with Acute Lymphoblastic Leukemia at age 24. They must learn to adapt to "medical life", putting their hopes and dreams on pause, navigating side effects and difficult emotions, and missing out on the beauty of every day moments that some may take for granted.

My ACE (Adverse Childhood Experience) score is 6. According to numerous academic studies, that puts me at risk for over 23 negative health outcomes, including diabetes, cardiovascular, digestive, respiratory and liver disease, cancer, and mental health issues such as anxiety, depression and thoughts of suicide.

“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.

Condamné par la maladie, Olivier Goy partage avec la journaliste Anne Fulda son inlassable combat pour mieux faire accepter le handicap et lever des fonds pour la recherche, et, surtout, appelle à regarder et aimer la vie pleinement?! Olivier a 46 ans quand on lui diagnostique la maladie de Charcot en 2020. Une maladie neurodégénérative qui se traduit par une paralysie progressive des muscles, mais laisse au malade ses pleines capacités intellectuelles. Espérance de vie?: 3 à 5 ans.

Salifu Sesay was but a toddler when a rebel attacker chose to plunge a machete into his skull. Against all odds, this victim of the Blood Diamond conflict in Sierra Leone, West Africa survived. A few years later, fate continued to intervene and Salifu was placed into the arms of Ann Miller, a woman from Overland Park, Kansas, whose life from that moment on, would never be the same. This is their mother/son love story.

The medical system took twelve years to reluctantly agree with Fay Martin that her husband was sliding into dementia. Even after he died three years later, people still questioned the diagnosis. This is an audiobook about what happens behind that veil of invisibility. Dementia Widow exposes, with courage and candor, the poison that seeps in, as a healthy reciprocal marriage becomes inexplicably hierarchical. Only when dementia is recognized as the villain does the relationship morph to offer the loving caregiving that enables a good final chapter.

A Life in Too Many Margins is a literary episodic tale featuring David, an autistic, chronically ill, and deeply exhausted queer individual. He's survived a few too many doctors with God complexes and an education system that couldn't accommodate a paper cut, let alone a brain like his. Now he's trying to keep it together long enough to get out and figure out what a life outside of survival mode even looks like.

Questo libro nasce dal bisogno di raccontare la quotidianità di una famiglia per tre quarti neurodivergente: e così, tra compiti a ostacoli e lettere che si rincorrono, prende forma un racconto vivo, umano, che mescola il memoir al consiglio pratico, l'esperienza personale alla riflessione condivisa; senza la pretesa di insegnare, ma con il desiderio di offrire uno spaccato di vita e uno sguardo onesto su ciò che significa convivere con la dislessia - da genitori e da figli -, affrontando le difficoltà ma anche valorizzando le risorse, i talenti, le prospettive diverse.