Disability Biography

Was zählt wirklich im Leben? Zuhören! Moderator und Youtube-Star Leeroy Matata teilt seine Erfahrungen mit uns. Hey Freunde, herzlich willkommen! Mein Name ist Leeroy und ich freue mich, dass ihr euch dieses Hörbuch gerade anschaut. Denn hier spreche ich so offen wie noch nie über das, was mich bewegt. Wir alle machen unterschiedliche Erfahrungen, die uns oft ein Leben lang prägen. Und niemand von uns kann in den Kopf anderer Leute schauen, deshalb führt das oft zu Missverständnissen. Aber das muss nicht so sein.

Jeremy Schreiber was on top of the world—athletic, newly married, successful. And then something went terribly wrong. In this moving memoir, he shares his journey after he received a terrifying diagnosis: ALS. As the devastating disease robbed him of movement and speech, he was abandoned by his wife and betrayed by a society that shuns people with disabilities. But it’s not all doom and gloom. He found love, support, and a powerful purpose. While fighting for his independence and then for his life, Jeremy gave his all to the ALS and disability communities.

This book is based on real-life events and is a raw and authentic account of a true fight for life and justice—a memoir of a mother’s love for her daughter, Rachel, who is diagnosed with severe cerebral palsy, a condition which makes her incapable of voluntary movement or speech. It tells of hopes and fears, and the true meaning of what it’s like to be the mother of a daughter with severe cerebral palsy. It portrays Rachel’s passion for life and her mischievous sense of fun.

Kelley Jo Burke embarks on a wild journey to understand many things, including the part where her grandfather sort of murdered her grandmother. Returning to a house filled with her first memories of childhood, she begins to explore the complex origins of her own anxiety. Along the way, she reflects on alienation and immigration, mental health and generational trauma, and the nature of memory itself. A memoir filled with raw honesty, comedy, tragedy, and grace.

Just before Christmas in 2012, at age 53, John LeMieux lost his left leg to a recurrence of sarcoma. The unique 20-hour rotationplasty surgery - never done on a man his age - was followed by six months of bed rest. It was only the beginning of years of physical, spiritual, and emotional growth. In this memoir, John recounts the lows and highs of a life forever altered.

An eight-year-old boy survives triple-limb amputation by freight train. One of America’s famous yet untold stories of overcoming the stigma of disability and responding with inspirational resilience. To change your perspective on life, listen now! Boy Interrupted takes the listener on Ricky’s remarkable journey of miraculous survival, the power of kindness, humor, mistakes, post-traumatic growth, and other surprises.

À 35 ans, Hugues réalise qu’il a vécu toute sa vie avec l’autisme (asperger) sans le savoir. Tous ses souvenirs sont à revoir à la lumière de cette nouvelle perspective. Il entreprend d’écrire une autobiographie dans le but de définir son identité, de construire enfin une histoire cohérente avec cette suite de souvenirs qui n’avaient jamais fait de sens.

Waste no day to achieve the impossible! When Pennsylvania started testing newborns for metabolic diseases, Adam Settle was one of the first to be diagnosed with Cobalamin-C Deficiency. Legally blind and mentally delayed, Adam never let his limitations hold him back from accomplishing his dreams. His love for people and his desire to help others comes through the sections of this audiobook. Whatever has been holding you back, this audiobook will help you charge through the obstacles you face to achieve the impossible. Adam’s story will inspire, encourage, and give you hope.

Jon Sadler was four when he had his first seizure following an episode of high fever. That made him the object of constant concern to his family and dictated almost every decision he made. With medication, Jon was deemed seizure-free for several years, though his speech was permanently affected. After a college sailing accident, he had his first grand mal seizure (loss of consciousness and violent muscle contractions).

After 30 years as a professor in the field of communication studies, Dr. Smith reminisces about some of his experiences and how his race and differently abled intersectionality have influenced documented encounters. As a Black and totally blind individual, he muses about how this distinction has both colored and shed light on what might have been innocuous or unremarkable encounters otherwise.

Axel Schylströms självbiografiska "BRÄND" är en handbok i motivation och mental styrka. Som nittonåring brännskadades Axel med tredje gradens brännskador över 70% av kroppskostymen. Ofrivilligt fick han spendera över ett års tid av intensiv fysisk och psykisk rehabilitering för att överleva. Trots ärren, handikappen och den ständiga motvinden kunde ingenting stå i vägen för Axels dröm om att bli artist, och idag är han en av Sveriges mest folkkära pop-hopp.

Meet Priscilla and Dave — two headstrong people with very different but complementary disabilities. When they met, fireworks flashed, but they soon became inseparable and each other’s "other half". Together, they attacked and overcame every obstacle in their way — and had one hell of a time doing it. Follow the story of their fiery love affair among moments of raucous laughter, fear, joy, sadness, and incredulity at people's behavior.

In 2018, Joe Hammond, wrote a piece for the Guardian about the 33 birthday cards he was writing for his two sons. It was shared by thousands. In A Short History of Falling he tells the story behind that piece, about the experience of living with - and dying of - motor neurone disease (ALS). A Short History of Falling is not a lament. It is a deeply imaginative meditation on what it feels like to confront the fact that your family will persist through time without you.

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.

On July 4th, 2013, Connor Sparrowhawk, also known as Laughing Boy or LB, was found dead in a specialist NHS unit. Connor, who had autism and epilepsy, had a seizure while in the bath, and no member of staff was on hand to stop him from drowning. An entirely preventable death. Sara Ryan presents a frank, sometimes funny and touching account of her son's early life and preventable death and the unfolding #JusticeforLB campaign.

A Michele La Pusata, dodici anni fa, è stata diagnosticata la Sclerosi laterale amiotrofica, meglio conosciuta come SLA. Prima, la sua era una vita più che normale, tra figli, lavoro e piccole incombenze, poi non lo è stata più. Non si mette mai in conto di affrontare una malattia lenta e invalidante come questa e infatti nessuno è preparato.

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."

Type 1 diabetic, fitness fanatic, dancing queen, Canasta champion; only some of the tags used to describe Colleen Ashby. Daughter, sister to five brothers, wife, and mother of three sons further define Colleen. Add to that, she is a heart transplant recipient who is now visually impaired, and you realize there is much more to learn.

When a devastating event takes away the way of life you are accustomed to, you have two choices: Stop living, or start planning! In this memoir, Shawn Paulsen demonstrates how he has overcome his stumbling blocks and turned them into stepping stones on his journey through the misfortunes of life. Shawn’s story inspires and motivates others to overcome. He describes how he has learned to face adversity with his chin up by taking a comedic view of his malady and life.