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Randy Pierce was 22 years old, fresh out of college, and thriving at an excellent job. His promising future seemed certain. Then, in just two short and devastating weeks, an unexpected neurological disorder plunged him into blindness. Randy, believing his future had vanished in the blink of an eye, wondered, “How can my life have meaning now?” Before he could fully answer, he had further to fall. Blindness was far from the worst challenge he would face. See You at the Summit is Randy’s uplifting personal account of his journey through adversity to accomplishment.

By the time native Sicilian Mariagrazia Buttitta turned 26, she’d planned out the perfect life. After finishing her residency in Buongiorno Medical School, she’d be primed for a job at the prestigious Roma Hospital, the first step toward becoming an Italian Dr. Oz. Instead, she wakes up to discover a medical diagnosis that leaves her almost completely blind. Her family, frustrated and desperate, seeks medical aid in the US, but it comes with a steep price.

Marilyn Elaine Lundberg’s true crime memoir, Jagger’s Eyes, is a brutally honest account of how one unfortunate little girl turned to animals for love, safety, and comfort. The trauma of incest and neglect occurred behind closed doors in her Christian home and crippled her psychologically as a child. Her attacks produced PTSD, suicidal depression, chronic anxiety, panic attacks, agoraphobia, anorexia, plus more, and she was housebound for many years as an adult.

I am a woman living with cerebral palsy (CP) since birth. When I was prepping for graduation and finishing my final honors essay for school, I had a realization that based on experience, most of the world does not think or experience life the way I do. Despite my CP, the world still didn't seem to process experiences, feelings, or ideas the same way I've learned to be my normal way of functioning.

The astonishing life story from one of Australia's most inspirational athletes. Dylan Alcott has never let his disability get in the way of what he wanted to achieve. His family treated him no differently to any other kid, and it was the best thing they ever did. Growing up, Dylan always had a positive attitude to life. So when he discovered sport, he’d have a go at anything and could always be found at the centre of the action, giving his best and playing to win. Then he tried wheelchair basketball and tennis and was hooked.

At 35, the same age as his mother when she had her accident, Mitch began experiencing symptoms of primary progressive multiple sclerosis, a particularly disabling form of MS, and his physical challenges grew to resemble his mother’s. In the ensuing years, he muddled through the ethical swampland of clinical trials, navigated the minefield of experimental treatments, and became a popular blogger and disability advocate. Equal parts entertaining and inspiring, Enjoying the Ride tells an extraordinary mother and son story.

At the age of 16, Marc Hoberman moved from Yonkers, New York, to Hollywood, Florida. Moving away from his friends was hard enough, but being diagnosed with epilepsy shortly thereafter was even harder. Marc’s story follows him from high school up to his present-day life as an author, teacher, husband, and father. His struggles with seizures, toxic medications, and loneliness were a certain recipe for disaster. Marc’s sense of humor, support network, and successful search for a doctor who would save his life prompted him to make his private story public.

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.

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.