Showing titles in People with Disabilities

Andrea Begley stunned the nation with her unique voice and was the brilliant winner of series two of The Voice UK. This is the exclusive story of her journey to the top. From her childhood in Ireland, coming to terms with the loss of 90% of her vision, to her university days and her passion for...

A young man once called unteachable journeys across America to investigate the lives of those, like himself, who are forced to create new ways of living in order to survive.  

This program is read by the author. Confessional and often hilarious, in Normal Sucks a neuro-diverse writer, advocate, and father meditates on his life, offering the radical message that we should stop trying to fix people and start empowering them to succeed. Jonathan Mooney blends anecdote...

Mothering under normal circumstances takes all you have to give. But what happens when your child is disabled, and sacrificing all you've got and more is the only hope for a decent future? Full of rage and resilience, duty and love, Ashley Bristowe delivers a mother's voice like no other we've...

Growing Up Disabled in Australia is the fifth book in the highly acclaimed, best-selling Growing Up series. It includes interviews with prominent Australians such as Senator Jordon Steele-John and Paralympian Isis Holt.

From Homer to Helen Keller, from Dune to Stevie Wonder, from the invention of braille to the science of echolocation, M. Leona Godin explores the fascinating history of blindness, interweaving it with her own story of gradually losing her sight. There Plant Eyes probes the ways in which...

Before a surfing accident caused thirty-three-year-old Devon Raney to lose all but 15 percent of his vision, he had already lived an extraordinary life. Time and again he'd gone against the grain to maximize time for his passions--surfing, skateboarding, and snowboarding--bringing him into the...

This English professor grew up spacey and overweight. Drowning in the unrealistic demands of motherhood, Livingston steals her son's ADHD medication and watches it transform her life—for good and bad. She grows weary of subjective diagnoses and chemical treatments from traditional psychology experts, and experiments with functional medicine—brain mapping and nutritional supplements—as a way to understand her brain's potential, bio-hacking her way to a healthy body and mind.

Un salto facile, provato mille volte in allenamento, qualcosa che va storto: un dolore insopportabile, il corpo che sembra finire all'ombelico, il terrore negli occhi del padre. A soli 16 anni Giulia Ghiretti passa dal preparare i Mondiali di trampolino elastico a un reparto di neurochirurgia. Il verdetto è crudele: non potrà più saltare, e nemmeno camminare. Ma niente può fermare Giulia, che scopre il nuoto, il suo nuovo sport.

O sonho de Juli era ser mãe e ela o realizou–e segue realizando diariamente–porém, ela não esperava os desafios que a maternidade atípica lhe reservava. O diagnóstico de Rafael veio no ano de 2015 e, de lá para cá, o hobby de Juli em escrever e influenciar pessoas teve uma mudança drástica: compartilhar tudo aquilo que estava reaprendendo com seu filho e sua família, fazendo-a acrescentar em seu currículo mais uma função: palestrante.

At 14-years-old, Karen Oliver’s son Ben was diagnosed with Friedreich's Ataxia, a rare genetic disorder affecting coordination and mobility and causes the development of cardiomyopathy and associated arrythmias. She was told he would be wheelchair bound by seventeen and live no longer than 34. But Ben was not going to let that stop him.

Der Autor lässt Erfahrungen sprechen, die er während seiner Arbeit als Alltagshelfer gesammelt hat. Dabei entstanden Geschichten, die nicht beschönigen und nicht urteilen, sondern in ihrer Ehrlichkeit berühren. Sie zeigen die Realität des Alters und die ungeschminkten Folgen von Krankheit, Verlust und Abhängigkeit. Doch zwischen all dem findet sich auch Wärme, Humor, Dankbarkeit und die Kraft kleiner Gesten. Jedes Kapitel offenbart einen Moment aus dem Leben eines Menschen, der gehört werden möchte.

" Bizarrement, en tant que société, nous accordons à la cécité un caractère bien plus dramatique que cette condition physique ne le mérite peut-être. Nous...

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.

Born with Epidermolysis Bullosa (EB), a rare and excruciatingly painful condition that makes her skin as fragile as butterfly wings, Emma Fogarty was not expected to survive infancy. Today, at 41 years of age, she is the oldest living Irish person with the condition, continuing to defy the odds with extraordinary strength, resilience and remarkable achievements. However, every accomplishment Emma makes comes with its own set of obstacles.

A touching and deeply personal memoir, Our Brother Jim recounts the author’s experience growing up with a brother with disabilities. Through his parents’ constant care and his family’s loving encouragement, Jim exceeded every doctor’s expectations, learning to do those “everyday” things that proved so difficult for him—like walking, counting, and communicating with others. With a radiant smile and a delightful sense of humor, Jim left a beautiful mark on the world around him. This book is to remember him.

Chef de groupe dans l’antenne GIGN de Guyane (ex GI2G), le major Franck Robin est un gendarme d’élite. Dans ce livre, il nous relate ses missions d’infiltration périlleuses au coeur de l’enfer vert de la jungle guyanaise pour traquer les garimpeiros, ces chercheurs d’or clandestins sans foi ni loi. Au cours d’une mission, il est blessé par balle et devient paraplégique. Désormais en fauteuil roulant, il refuse que ses enfants le voient comme un handicapé, eux qui le considéraient jusqu’alors comme une sorte de super-héros.

When Roger Rasmussen was diagnosed with prostate cancer in 2019, he did what most patients do: listened carefully, weighed his options, and tried to make peace with the life-altering decisions ahead. Then he heard about Joe Tippens' story, which led him down a rabbit hole of research into something unexpected—a compound called fenbendazole with curious case reports and a growing collection of personal accounts.

Philippe Croizon roi de l'humour ! Philippe Croizon n'est pas un être comme les autres ! Son histoire dramatique est devenue sa force, son moteur, sa raison de vivre. Amputé des bras et des jambes, il a pourtant décidé de rire de tout, et tout le temps ! Si ses exploits sont régulièrement les "Unes" de la presse (Dakar, traversée de la Manche...), Philippe est connu pour son humour sans limite et sans filtre ! Cet humour, il nous le livre pour la première fois dans ce livre qui va mettre à rude épreuve vos zygomatiques.

This is the biography of a young man with some neurological differences, written in the first person. Through his eyes, we see how he perceives his life and negotiates his reality. His world and his understandings of life may be different from the norm, but we learn to appreciate a special type of soul that should be acknowledged and celebrated as part of human diversity. This book demonstrates the love and nurturance of his mother and the dynamics of his relationship with her. We also enjoy hearing about the comfortable lifestyle that Marcelo has been given, including his worldwide travels.