Disability Biography

Mit 15 Jahren verliert der Deutsch-Singhalese Saliya Kahawatte innerhalb von Monaten einen Großteil seines Augenlichts. Die Ärzte sagen, dass er eines Tages völlig blind sein wird. Er soll die Schule verlassen und in die Blindenwerkstatt, er aber träumt von Abitur, Studium und selbstbestimmtem Leben. 15 Jahre lang verschweigt er seine Behinderung, um in der Welt der Sehenden Karriere machen zu können. Fingerspitzen, Ohren und seine Intuition ersetzen seine Augen.

Blaze Ginsberg offers a unique view into his mind and life as a high functioning autistic teenager. Inspired by the format of the Internet Movie Database, Ginsberg organizes the events in his life as a collection of "episodes." Some of these are ongoing (like Thanksgiving dinners with his family), some are in syndication, and some (his crush on Hillary Duff, for example) have sadly come to an end. Using a style and a language all his own, Blaze reinvents the traditional memoir for listeners of all ages.

Blind from birth, Graeme Innes was blessed with a family who refused to view his blindness as a handicap, instilling in him a belief in his own abilities; blessed with a determination to persevere. After a long and successful career as a lawyer, company director and Human Rights Commissioner, Graeme has written his story. Finding a Way shares his memories of love and support, challenges, failures and overcoming the discrimination so many people with disabilities face.

In the mid-1970s, brothers Buddy and Jimmy Miley were close, both on the verge of impressive athletic careers. A promising high school quarterback, Buddy's potential was cut short by an injury that left him quadriplegic. Immobile and imprisoned in his body for decades, Buddy would watch life pass by from his wheelchair, living at home under his mother's and brother's care and wondering what his life could have been.

Gradually going blind in his 20s, Rich Ruffalo refused to face reality. And then, one rainy evening, unable to make sense of the road before him, he suddenly felt his car thud against a little girl. Jolted into reality, Ruffalo refused to be knocked down and, instead, put his all into achieving. As a teacher he excelled, winning the Princeton University Distinguished Secondary School Teacher of the Year Award and Disney's Outstanding Teacher of the Year Award. Then, he set the bar even higher.

A young man with special powers is forced to retire from a life of violent crime and escape from New York City at the age of 18. He gets his life together and becomes a respected physician. Thirty years later, he is afflicted with a mysterious illness silently sweeping across the globe. While desperately struggling to find redemption and a cure, he learns that violent associates from his past and federal law enforcement agents are still relentlessly in pursuit.

The world spun and rolled as I collapsed at Macy’s in San Francisco to the voices of Christmas carols being sung and bells ringing. Fresh out of the ICU and a week later, a beige man gave me a beige folder with a dark diagnosis that would color the rest of my life - multiple sclerosis. This set off a tidal wave, a tsunami inside of me that ravaged my body and crushed my lungs. The MS Diaries is a memoir that seeks to impart the journey inside one man’s mind struggling with a severe chronic illness through uncensored personal anecdotes and humorous situations.

They say if you want to make God smile, tell him you have a plan. Dwight’s plan was to live his dream, teach math, coach football, and build a comfortable life for himself. Fate had other things in store for him. The story of Dwight’s physical and emotional journey from life as an able-bodied young man chasing his dreams only to have his world turned upside down by the thoughtless act of a 71-year-old drunk driver.

In No Bad Days, JT details the incredible story of how he overcame what seemed like insurmountable odds and shares the many invaluable lessons he has learned throughout his life in the hope that others might reach their full potential. These lessons include how to: find your tribe, pull off the label, stretch yourself, listen to others, and learn to fall. JT’s improbable life story is evidence that regardless of the mental and physical challenges you might face, you can defy the odds to create the life you want and accomplish the things you’ve only dreamed about.

Look at It This Way answers questions we all may have been reluctant to ask, it gives us a glimpse into what blind people experience living in a sighted world, and it breaks through barriers that may cause people to think that differences equate to superiority or inferiority.

A profoundly beautiful memoir about disability, difference, and living as a vulnerable body. Jan Grue had just become a father when he inherited a stack of his childhood medical records. Following a diagnosis of spinal muscular atrophy at the age of three, the raft of doctors' notes, clinical descriptions and case histories defined his body as defective and his future as bleak and limited. They conjured a childhood nothing like the one he remembered, that failed to anticipate the life he lived now. "I Live a Life Like Yours" is Grue's beautiful, groundbreaking search for a literary language that could better tell his story.

Essere una donna disabile in un mondo in cui l'immagine femminile appare sempre patinata e perfetta non è facile, ma Antonella Ferrari, attrice e ballerina, malata di sclerosi multipla, non si è mai arresa tanto da diventare un punto di riferimento, una fonte di ispirazione per tante persone meno fortunate. "Mi sono beccata tantissime porte in faccia, tantissime delusioni ma dovevo andare avanti anche per tutti quelli che vivono bloccati per colpa di una malattia."

James Partridge was 18 years old in 1977 when his face and body were severely burned in a car accident. Refusing to succumb to society's expectations, James chose not to hide in the shadows, but to succeed despite his distinctive face and live a happy and hugely successful life, both personally and professionally. Face It tells the story of James' recovery and the work he has done ever since to support others with physical differences to cope with the isolation and discrimination they so often face.

Do you know an adult with autism, Down syndrome, or another special need? One in eight people on our planet live with some form of disability. And they all deserve to live productive, engaged lives. Are we willing to help them accomplish this goal? The mother of an adult with autism, Andrea Moriarty leveraged her son’s passion, talent, and personality to help him create an out-of-the-box vocation: A podcast. After more than 80 interviews, she recognized three vital attitudes that people with disabilities teach us - risk taking, humility, and kindness.

This honest, outspoken, and thought-provoking memoir by award-winning writer and appearance activist Carly Findlay will challenge all your assumptions and beliefs about what it is like to have a visibly different appearance. Carly lives with a rare skin condition, Ichthyosis, and what she faces every day, and what she has to live with, will have you cheering for her and her courage and irrepressible spirit. This is both a moving memoir and a proud manifesto on disability and appearance diversity issues.

Mehr als nur ziemlich beste Freunde... Mit 16 erleidet Justin einen Verkehrsunfall, der ihn fast tötet und eine langsam voranschreitende Autoimmunerkrankung auslöst. Er kann seine Arme und Beine nicht mehr bewegen, ist auf den Rollstuhl angewiesen. Sein Traum: den Jakobsweg gehen. Als er seinem Freund Patrick davon erzählt, zögert dieser nicht, sich mit ihm zusammen auf das Abenteuer einzulassen. Sechs Wochen sind die beiden unterwegs, die Reise bringt beide an ihre Grenzen, doch gemeinsam bewältigen sie die 800 Kilometer über Stock und Stein durch Nordspanien.

Shortly after his daughter, Leontine, was born, Christian Donlan's world shifted an inch to the left. He started to miss light switches and door handles when reaching for them. He would injure himself in a hundred stupid ways every day. First playful and then maddening, these strange experiences were the early symptoms of multiple sclerosis, an incurable and degenerative neurological disease.

Quentin Kenihan is living proof that superheroes don't need capes, just the right attitude. When he was a kid, Quentin loved Superman. Ironic, really. Quentin didn't need kryptonite to reveal his weakness - born with a rare bone disorder, osteogenesis imperfecta, his bones broke all on their own. When Quentin was seven, Mike Willesee made a documentary about him. Australians fell in love with his wit and never-say-die attitude. Over the years he grew up before our eyes. But there was a dark side to his life. The true story was never told...until now.

Hearing Maud: A Journey for a Voice is a work of creative non-fiction that details the author’s experiences of deafness after losing most of her hearing at age four. It charts how, as she grew up, she was estranged from people and turned to reading and writing for solace, eventually establishing a career as a writer. Central to her narrative is the story of Maud Praed, the deaf daughter of 19th century Queensland expatriate novelist Rosa Praed.

Just when life seemed rosy and the sun was shining, Dr. Bhaskar Bora sustained a severe spinal cord injury in July 2019 following an operation, which left him with paralysis of both legs, a nonfunctioning right hand, and a long stay in the hospital, eventually leading to a forced medical retirement from his medical career and a wheelchair in place of a sports car. Poorer financially but richer in experiences of life, he is now a voice for the disabled and has written the book The Second Chance in Life as an honest reflection of his life experiences.