Disability Memoir

Nadeem's journey is a story told by a mother about her son—it’s not just about a mothers love, it also shows his compassion towards her, his siblings, family and friends. It shows us how he never let his illness define who he was even when the doctors were curt and less kind with their delivery of information. This book tells us the story about a fight to survive, a story about a mother’s love for a child and a story about how a community comes together to support each other.

Told through an experimental mix of intimate anecdotes and interactive visuals, this book immerses listeners in Emmy Award–winning documentary filmmaker James Robinson's point of view, allowing them to see the world through his disabling eye conditions.

Public Hostage, Public Ransom starts with the autobiographical story of William Bronston, the activist physician whose early professional California training steels him with a deep moral, professional, and cultural bond to the huge 6,000-person disabled population he encounters incarcerated in Willowbrook State School in Staten Island, NY, on whose behalf he daily battles to humanize and ultimately catalyze a federal class action lawsuit against the state to close the death-making institution.

Tracey had been told this so often as a child. Yet, two months after the horse-riding accident, Tracey was still not able to fulfil it. In fact, at that stage, she couldn’t do anything for herself. You’d think that after nearly losing her life and her abilities to live life as it was before because of the riding accident, that she’d be nervous about getting back on a horse. But her love for horses and riding was so deeply ingrained within her that she couldn’t imagine a life without it. Getting back on a horse...she was determined that she would.

You are more than your limits. Choosing to see herself as more than a person with a disability and wheelchair user, Lolo chooses to live a bold and courageous life now because representation matters. She created this intersectional guide to provide tools for people with disabilities to thrive in personal growth, independence, and community building. Add this guide to your list of inclusion books!

Af's journey starts from the exhilaration of the Rio 2016 Olympic Games to confronting a tumour diagnosis at 29. An unexpected return to the UK meant trading Olympic thrills for surgeries and chemotherapy. This isn't just a tale of medical battles but family relationships, friendships and positivity. Af shared his journey on social media with an unfiltered look into the world of cancer treatment. Set against the vibrant backdrop of Brazil and the medical corridors of UK hospitals, Af's tale is one of resilience, humour, and hope.

Already facing a wretched cancer diagnosis, a young man’s prospects for survival dim as he learns his treatments have not worked. Writing against the clock, he feverishly authors a story of profound joy and sadness exploring the life he could have lived. Desperately told, his story takes you through poignant memories, intimate relationships, and fantastical triumphs in a quest to make sense of it all and leave a legacy behind.

As a 14-year-old psych ward patient, Harry realized he had a choice: let anorexia keep ruining his life or fight back against everything his mind told him was true. Now 22 years old, Harry delicately pieces together how his mind derailed to that point, what’s happened since he made his choice, and most importantly, what it’s taught him about life and how best to live it.

Andrea struggles to mourn a man who is still alive as she witnesses her father decline into the depths of Alzheimer's. Denial and devastation color her life when she learns her father, Richard, a recently retired surgeon, is diagnosed with Alzheimer's at the age of 67. Her dream to grow closer to him is crushed as the reality of his disease is fully realized. Andrea, a mother of three young children, learns to balance motherhood with daughterhood as she grapples to accept her father's fate.

Sent blind soon after birth, David Hume stubbornly refused to live the limited life well-meaning elders and social norms expected. To date, that encompasses years in a blind institute, two marriages, grieving for two outstanding wives, founding recruiting firms, devising marketing techniques, facing business collapse, sailing ocean races, and through much of it, being the lead singer in popular bands. If you enjoy a short biography that inspires, saddens, cheers, and sticks in your memory, then don't put aside Blind Without Barriers.

Hall is authentic, transparent, and raw as she shares the many facets of her dynamic life and colorful personality. The chapters are like peeling an onion as Hall deftly delivers the most dismal times of her life. Listeners will experience so many emotions but will ultimately cheer for Hall’s escape, redemption, and power to rebuild a successful life. She credits her beloved 93-year-old grandmother's unconditional love and wisdom for giving her the endurance and strength to overcome all that life has dealt her.

Henry Markram is the Elon Musk of neuroscience, the man behind the billion-dollar Blue Brain Project to build a supercomputer model of the brain. He has set the goal of decoding all disturbances of the mind within a generation. This quest is personal for him. The driving force behind his grand ambition has been his son Kai, who has autism. Raising Kai made Henry Markram question all that he thought he knew about neuroscience, and then inspired his groundbreaking research that would upend the conventional wisdom about autism, expressed in his now-famous theory of Intense World Syndrome.

This is my story. After a lifetime of trying to help everyone else get their lives together, I have finally figured out how to get mine together. I am now 72 years old, semi-retired from a business I created to help young adults with autism function in the world. I live in Mexico with my loving partner. I have fulfilling relationships with my adult children and grandchildren.

Many people give up on God. It’s easy to trust in his goodness and strength when life is easy. But how do we persevere in our faith when life gets hard? Few people can show us how to do that better than Allan Schwartz.

Mit drei Jahren erlitt Ingrid Mundschin-Bohn eine Hirnhautentzündung, an der sie fast gestorben wäre. In Deutschland, wo sie als Tochter eines deutschen Vaters und einer Schweizer Mutter aufwuchs, war gerade der Krieg zu Ende gegangen, die Medikamente waren immer noch knapp, und die Ärzte wollten keine Antibiotika verschwenden an einem Kind, das in ihren Augen bereits abgeschrieben war. Aber Ingrid Mundschin ließ sich nicht abschreiben, sondern wuchs zu einer lebensfrohen und selbstbewussten Frau heran.

This is a guide for anyone going into a mental asylum or institution for the first time, or if you have a delusional loved one, with a mental illness, this will help you relate to them better in understanding insanity. Now, join me, in the asylum, as together we go on a very odd journey of discovery in my first mental institution experience. Enter a strange world, before I was diagnosed with schizophrenia, as I compete against other game show contestants in a battle to win genetic traits for my family tree.

When I was six years old, I started wearing glasses. My view of my low vision quickly changed when I was twenty years old and found out that my brother had suddenly gone blind. He was told that he was suffering from Retinitis Pigmentosa (RP), a disorder that slowly destroys the pigment cells in the eyes. So far, there are no known cures. At the tender age of twenty-one, I was also diagnosed with RP. Since then, I have been slowly going blind, not knowing when my world would finally fade away forever. Battling against such a crippling disease led me through a labyrinth of challenges.

Es ist Nicoles zweiunddreißigster Geburtstag, als sie unter der Dusche steht und sich auf die Feier mit ihren zwei kleinen Kindern und ihrem liebevollen Mann freut. Abrupt wird sie aus ihren Gedanken gerissen, als sie einen Knoten in ihrer Brust ertastet. Eine Welt bricht für sie zusammen. Später stellen die Ärzte die Diagnose, dass in Nicoles Körper nicht nur ein hochaggressiver Tumor wächst, sondern dass sie außerdem dieselbe genetische Vorbelastung wie Angelina Jolie hat. Selbst nach erfolgreicher Therapie, bleibt die Wahrscheinlichkeit einer erneuten Erkrankung enorm hoch.

This often heartbreaking account by Carol, whose son, Paul, was born with many difficulties, including autism, is told with the honesty and sincerity necessary to portray the conflicting emotions faced by any family, and particularly a mother, in such circumstances. The overbearing feelings of guilt, failure and inadequacy have to be resolved to enable a happy life with her family.

Graham Hale Gardner died before turning 23 and never learned to walk or speak due to severe cerebral palsy complicated by epilepsy. Yet he left a legacy of love and compassion that deeply moved scores of people from widely different backgrounds. Graham’s story, written through the eyes of his father, speaks of the enormous legacy left by a boy who never spoke. A story that raises provocative questions about the “invisible lines of connection” that make us human.