Showing titles in People with Disabilities

Living in the Belgian Congo with her husband in the 1960s, Fran’s mother became pregnant with a daughter. However, right after she gave birth in the hospital, she felt strange. Unbeknownst to anyone, another daughter was on the way, but before anybody responded, an hour had passed. Because of the delay, Fran was born with cerebral palsy. Growing up with her siblings in Africa, Fran always felt different. When everyone else was playing and having fun, she would watch and wish she could join in.

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.

On an island off the coast of Massachusetts, six miles across the cobalt blue Waters of the Nantucket Sound, there is a place where hope flourishes. The island is Martha’s Vineyard. The place is Camp Jabberwocky, a sleepover summer camp for people with a variety of disabilities.

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.

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.

In "Not Now Please: Living through Racism, Ableism, and Grief," Elizabeth takes you on an intimate journey through the intersecting worlds of adversity, resilience, and transformation. This compelling narrative is a candid exploration of personal experiences that touch upon the deep-rooted issues of racism, ableism, and the complexities of grief.

" 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...

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.

Imbalanced traces Sheri Thomas' remarkable journey from a front-page headline in 1962 to her current role as an advocate fighting to remove the stigmas surrounding physical disabilities and mental health.

Helen Keller’s name is forever linked with courage, perseverance, and the power of education. In Midstream: My Later Life, she picks up where The Story of My Life left off, offering a rare look at her journey beyond her early triumphs. Here, Keller recounts the challenges and victories of adulthood—her advocacy for people with disabilities, her international travels, her friendships with world leaders and artists, and her tireless fight for social change. She writes candidly about setbacks, loneliness, and the weight of public life, but also about the deep sense of purpose that guided her.

Damiano e Margherita sono due fratelli che hanno molte cose in comune: la voglia di mettersi in gioco, la caparbietà e la tenacia nel voler inseguire i propri sogni, e l'autismo. Insieme si sono esibiti in televisione e, mano nella mano sul palcoscenico, sembrano finalmente aver trovato il loro posto nel mondo. Già dalla mattina successiva, però, i due sono obbligati a tornare alla realtà. Damiano vive a Rimini e ha le idee molto chiare sul futuro: una moglie – "l'altra metà della mela" – con cui avere dai dodici ai venti figli, milioni di dischi venduti, concerti in tutto il mondo.

Most people encounter disability at some point in their lives, either in their own bodies or through a friend or loved one. Faith leaders, sacred texts, and members of religious communities frequently offer religious teachings and metaphors as explanation for the presence of disability, but rarely do we hear the voices of people living with disabilities reflecting on their experiences of God, faith, or religious life.

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.

Tara Sidhoo Fraser is thirty-one years old when a rare mutation in her brain causes a stroke. Awakening after surgery with no memory of her previous life, she attempts to piece it all back together through a haze of amnesia. Yet, as memories do begin to surface, they are seen through someone else's eyes—the person whose body she stole, whom she calls Ghost.

Hilda’s family didn’t know she had muscular dystrophy. They just knew their preschooler was losing her ability to walk. But they were determined to find a cure. Being disabled in Cameroon meant not only obstacles to transport, but visits to diviners and evangelists, threats of sexual assault, discrimination, and a crisis of faith. Despite the hardship Hilda has faced, her family’s unwavering support and God’s unwavering grace have helped her persevere to become a national broadcaster.

Have you ever been around people, yet still felt alone? Dr. bird has too. Within the first variant of their envirusmental series, they revealed thirty years of their late-in-life realized secrets. In this second volume, they, literally and figuratively, Zoom in on the last four "unprecedented" ones. This includes them cutting-the-s--t about how, half-way through their PhD, COVID-19 hit. And how, a couple years later, they added "Dr." to the front of their nickname.

A revelatory collection of essays on the DeafBlind experience, and a manifesto on the power and untapped potential of touch. Born Deaf into an ASL-speaking family and blind by adolescence, John Lee Clark learned to embrace the possibilities of his tactile world. He is on the frontlines of the Protactile movement, which gave birth to an unprecedented tactile language and a way of life based on physical connection.

“Canal dói?” “O que é que eles fazem no Japão?” “Os Menudos são legais?” Stella Estrela não se dedica a responder nenhum desses questionamentos, mas a apresentar a autora dessa lista tão peculiar de perguntas. Stella nasceu com a síndrome de Williams-Beuren, uma desordem genética rara que impôs, de saída, enormes desafios a ela e a seus pais.

«Sono Rachele e ho 29 anni. A un mese dalla nascita, è stato detto ai miei genitori che avevo la fibrosi cistica, una malattia genetica degenerativa da cui non si può guarire. La malattia non si vede perché colpisce principalmente gli organi interni; tutte le secrezioni sono alterate e molto dense, il muco ristagna ed è difficile respirare. Quando sono stata invitata a un evento della Fondazione per la Ricerca sulla Fibrosi Cistica, mi sono chiesta: come faccio a unire la mia passione per i motori con quello che mi sta più a cuore?»