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At birth, few people knew if Scotty Crabtree would live past infancy. Growing up with cerebral palsy, his future was uncertain. Thanks to the company of family and friends in the Bakersfield community, he would be “just fine”. Despite losing loved ones, undergoing painful surgery, and life’s daily obstacles, Scotty believes in celebrating life and pursuing his dreams as a country music artist - especially since the fateful night one man told him one thing: “You can do anything you set your mind to....”

Life moves fast. Too fast for some people. This is the true story of what it's like to live in a world where you can't keep up. Bobby was ten months old when my mom and dad rescued him from birth parents who were slowly killing him. He was adopted into our family after a lengthy custody battle. Instead of that settling him, it set off a lifelong struggle to find a place to belong, a place to call home. Like an old-fashioned merry-go-round, the world moved at a speed that was just too fast for Bobby. He couldn't keep up, which prevented him from keeping a job.

Theresa Marafito, daughter of Irish immigrant parents, was born in 1933 in New York City, blind in one eye with partial vision in the other. She was a precocious child who wanted to appear “normal” to her peers and family, regardless of her disability. Her game was to be independent, not dependent, and would rarely ask for help. At 19, she graduated magna cum laude with two master’s degrees. Theresa and her husband, Jerry, who was also visually impaired, would build a house on a shoestring budget and had two daughters; one who was also born visually impaired.

Unser heimlicher Star in der Hörbuchreihe "Die Runde Ecke" hat das Tourette-Syndrom. Eine Krankheit, die durch sogenannte Tics charakterisiert ist. Jean-Marc sagt über sich: "Wenn es morgen eine Wunderpille gäbe, ich würde sie nicht nehmen." "Tourette in my head" ist eine berührende Mischung aus motivierenden Gedanken und tiefem Vertrauen in das Leben. Das Hörbuch erzählt von persönlichen Abstürzen, Neuanfängen, skurrilen Momenten und besonderen Triumphen.

Ein persönliches Plädoyer für Toleranz und Freude am Leben Menschen tätscheln ihm den Kopf oder starren ihn an - Raúl Aguayo-Krauthausen, der aufgrund seiner Glasknochen im Rollstuhl sitzt und kleinwüchsig ist, weiß, dass viele Menschen Schwierigkeiten haben, mit Behinderten unverkrampft umzugehen. Dabei ist jeder zehnte Deutsche behindert, da sollten wir uns doch eigentlich an den Umgang mit jenen gewöhnt haben, die nicht "normal" sind.

À travers cet ouvrage, c'est un véritable message de courage et de persévérance que nous délivre Vincent. Mais plus encore, il nous offre son inspirante philosophie de vie et nous incite à ne jamais abandonner nos rêves et à aller au bout de nos passions. Vincent Vinel a sans conteste été la révélation de la soirée d'ouverture de la saison six de "The Voice". Devant plus de 6,8 millions de téléspectateurs, ce jeune chanteur malvoyant a d'emblée conquis les coaches.

Ben Mattlin lives a normal, independent life. Why is that interesting? Because Mattlin was born with spinal muscular atrophy, a congenital weakness from which he was expected to die in childhood. Not only did Mattlin live through childhood, he became one of the first students in a wheelchair to attend Harvard, from which he graduated and became a professional writer. His advantage?

La réalité quotidienne d'un non-voyant est un pays étranger. Quel est son rapport au monde ? À la ville et à la nature, à la nécessité de se déplacer, d'utiliser des écrans tactiles, de traverser les rues, de reconnaître les gens ? Invité à donner des cours au Québec, l'historien Jacques Semelin nous propose un récit de voyage d'un genre nouveau. À la fois le sien, dans une ville dont il découvre tout, et le nôtre, dans la tête et le corps d'un non-voyant.

Le 3 avril 2015, on diagnostique à Marine, jeune étudiante dynamique de 21 ans, une sclérose en plaques, appelée plus communément SEP. L'urgence de la situation, le besoin de prendre une décision quant à la prise d'un traitement ou non et le manque d'informations, l'amène à s'interroger. "La maladie c'est toi qui l'as, il faut donc chercher la solution en toi." Son traitement ? Réaliser un projet rêvé : le voyage.

"Je vis avec l'autisme", écrit Josef Schovanec, soulignant ainsi ce qu'il considère plus comme une qualité que comme un handicap. Ce voyageur passionné des civilisations anciennes maîtrise une dizaine de langues, est diplômé de Sciences Po et possède un doctorat en philosophie. Il récuse pourtant les attributs qu'on lui prête - ceux d'un autiste "génial" aux capacités intellectuelles extraordinaires - pour évoquer plutôt, avec beaucoup d'humour et de sensibilité, ces "petits" problèmes qui font le quotidien d'un autiste Asperger.

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.

February 29th is a date that comes into existence just once every four years. It is also the birthday of Thais - author Anne-Dauphine Julliand's darling daughter - who died of a genetic disease. Thais lived just shy of her fourth birthday. She had a short life but good one. As this special day is about to reappear on her calendar for the first time since her daughter passed away, Anne-Dauphine struggles with how to mark this momentous occasion. She wants to live fully on this special day: Thais would have been eight years old.

In the spring of 1974, as the last American troops were being pulled out of Vietnam, Ron Kovic and a small group of other severely injured veterans in a California VA hospital launched the American Veterans Movement. In a phenomenal feat of political organizing, Kovic corralled his fellow AVM members into staging a sit-in, and then a hunger strike, in the Los Angeles office of Senator Alan Cranston, demanding better treatment of injured and disabled veterans.

In 1997, Daniel Trush, a bright, active, outgoing twelve-year-old, collapsed on the basketball court and fell into a deep coma. Rushed to the hospital, he was found to have five previously undetected aneurysms in his brain. One had burst, causing a massive cerebral hemorrhage. While Daniel remained comatose, the uncontrolled pressure inside his skull caused him to suffer multiple strokes.

Vision in the Dark is Dr. Andre Watson's story of becoming a blind visionary. He is blind, yet he decided to use his life to develop new ways of seeing himself, others, and the world. Andre braved and overcame countless odds. Today he is a licensed clinical psychologist, a world traveler, an award-winning athlete, and a beloved husband, father, and friend. He offers a challenging and awe-inspiring glimpse of life through the eyes of a blind man.

In the context of bulling, we tend to focus on the don'ts. Don't point. Don't stare. Don't use hurtful words. Being the eternal optimist that he is, Joe challenges us to redirect our energy. Instead of not acting like a bully, he calls us to imitate the compassion of a friend. Subtle yet powerful, the examples Joe gives of people going out of their way to treat him like they would anyone else call all of us to action.

After you're done listening to Glenna's story, you cannot help but admit she's led a hard life. She's gone through more than her fair share of trouble, in different ways. Some of it she invited; some she did not. To say that she had a troubled childhood would be an understatement. Cutting a long story short, she spent a considerable time working as a prostitute. She was a drug addict. Somewhere along the way, she caught AIDS and Hepatitis C.

As a US Army infantryman in World War II, Don Wedewer was twice wounded in four days. On both occasions, he was left for dead. Now he was a double amputee and blind with seemingly no hope for the future. Yet through extraordinary determination and persistence, this highly decorated combat veteran overcame seemingly impossible odds to become a state and national leader in providing opportunities for those with visions loss. This is Don Wedewer's story. For more information visit www.bravestguy.com.

When adventurous overseas traveler, Amy, is diagnosed with retinitis pigmentosa, she has no idea what difficulties lie ahead. After finishing mobility training from the Bureau of Blindness, she thinks her problems are solved, but when Amy tackles the streets with her white cane, the real fun begins. Determinedly sweeping away her fears, she starts to celebrate the reality of vision-impaired independence. Join the chaos and laughter in this series of uplifting anecdotes as Amy looks to the lighter side of mobility.

The life of Dr. Scott Hollier is not what you'd call typical. He is well-educated, has a good job, is a husband and father, is legally blind, loves computers and gadgets, goes to church, and enjoys travel, spending time with friends and following his favorite football team. For most people, the atypical part of this description will be "legally blind", but from Scott's perspective, it's his traitorous support of a football team outside his home state of Western Australia that makes him stand out from the crowd.

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.

After two decades of suffering with the mental disorder known as obsessive-compulsive disorder, Derek has reached his breaking point. His past attempts to find inner peace had lead him astray. At last he longs for a life of ease and tolerance without the handicap his illness brings. Enter the next phase of his life as he copes with obstacles ahead in this true story. Follow his path to recovery as he seeks help, wisdom, and clarity to rise above what has grounded him for so long.

In a series of beautifully textured stories, the author takes the listener on a fascinating journey as she travels with Teela, her lively "golden dog", through airports, city streets, and southwest desert landscapes, exploring these surroundings with changed sight. This unusual account of travel will inspire the sighted as well as the blind, offering pointed observations on processes of learning to work with a service animal and on coming to terms with a disability.

In August 2007 Dianne Woodford woke up to find that she had lost her sight overnight at the age of 38. A type one diabetic since the age of 13 and a single mother of three, Dianne was determined not just to accept it and let people care for her. Instead she set up her own charity to help others in a similar situation and began her own journey to independence with a little help from Hattie, her guide dog.

A Rocky Start feels like a potential classic: an authentic treatise on the state of America's mental health establishment and the help or damage it metes out to people who desperately need its services, written by someone who knows that world intimately, from inside both its real and perceived walls. Fisher describes A Rocky Start as "a candid and rare look into one particularly complex life." It is that and more. Fisher's natural intelligence drives the narrative.

Don entered the workforce as a young man barely out of high school, full of enthusiasm and idealism. He soon received a reality check about corporate America. Raised in the middle class, he believed in the value system of an honest day's work for an honest wage. That by doing what was "right" and working hard, he would succeed. The Company Store, however, had other plans for him and his coworkers - the American working class.

La tarde no habiacute;a comenzado de esta manera.

Eight Fingers and Eight Toes: Accepting Life's Challenges is a story of the power of a mother's love for her children and her journey of self-love. It is a story of struggles and learning to accept and overcome challenges. One takes a front row seat as the author learns answers to questions asked decades ago that result in part from the family being the first ever to have their entire genome sequenced.

My name is Joseph A. Peragine, and I am a paranoid schizophrenic. On October 22, 2000, I tried to kill myself in a severely hallucinogenic state due to undiagnosed paranoid schizophrenia. I was suffering from this illness for many years leading up to that day. Every October since I started my recovery in 2000, I reflect on my life and am extremely thankful that I was fortunate enough to have been given a second chance. Every October, I especially make it a priority to tell my family and loved ones how much I love them.

Adventurous international teacher, Amy Bovaird, is diagnosed with Retinitis Pigmentosa, a hereditary eye disease that will blind her. In spite of that, she manages to continue teaching overseas. Then her father's final illness brings her back home for good. There, friends and acquaintances begin to notice that she doesn't always recognize them and sometimes stumbles as if drunk! Insensitive students ridicule her in the classroom.