Títulos em Pessoas com Deficiências

Gracie wrote Comfort in Darkness after being diagnosed with Parkinson’s Disease, a terminal sentence which he views as the greatest fight of his life, one he knows he will eventually lose. This is Gracie’s defining life statement about his spiritual and technical practice. For the first time, he reveals his time-tested theories and techniques of invisible Jiu Jitsu, a combat system anyone can use to awaken their power and apply it to their everyday lives. An indispensable tool for any fighter or seeker, Comfort in Darkness teaches how to balance and align the mind, body, and spirit.

After years of unexplained health problems, Polly Atkin's perception of her body was rendered fluid and disjointed. When she was finally diagnosed with two chronic conditions in her thirties, she began to piece together what had been happening to her - all the misdiagnoses, the fractures, the dislocations, the bone-crushing exhaustion, the not being believed. Some of Us Just Fall combines memoir, pathography and nature writing to trace a fascinating journey through illness, a journey which led Polly to her current home in the Lake District.

Escrito quando Naoki Higashida tinha apenas 13 anos, o conjunto de ensaios reunidos neste audiolivro conta, do ponto de vista do próprio Higashida, a experiência de ser autista. Preso em seu mundo individual, muitas vezes ele exibe comportamentos vistos como estranhos, peculiares, “inadequados”. Seja repetindo palavras e frases aparentemente sem sentido ou evitando contato visual com outras pessoas, Naoki tem uma enorme dificuldade de se comunicar e de socializar.

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.

Temple Grandin, Ph.D., is a gifted animal scientist who has designed one third of all the livestock-handling facilities in the United States. She also lectures widely on autism - because Temple Grandin is autistic, a woman who thinks, feels, and experiences the world in ways that are incomprehensible to the rest of us.

After losing both legs from the pelvis down at the age of five, Spencer West tackled challenge after challenge, learning to navigate a world set against those with disabilities. In this deeply personal and transformative guide, he reveals how he stopped living by the expectations of others and instead embraced his true identity, passions, and purpose.

“I was twelve when they locked me away. They didn’t give me therapy though. They gave me trauma.” Broken Doll is a brutally honest collection of poetry and artwork created from inside the walls of psychiatric institutions. Written by Michelle, a survivor who spent her entire adolescence sectioned in mental health units, this book lays bare the pain, confusion, and silent fury of growing up in a broken system. Through raw, emotionally charged poems and haunting original artwork, Michelle documents years of systemic abuse, isolation, and resistance.

In this awe-inspiring memoir, Nalevate, Lanale Robinson shares his breathtaking journey of resilience, determination, and triumph. Diagnosed as a quadriplegic after a life-altering accident. Lanale defied the odds, and rose above challenges. Today he walks, a living testament to the boundless potential of the human spirit.

Gaelynn Lea was born with Osteogenesis Imperfecta. Her parents were loving, cash-strapped theater kids, and she grew up racing about in her first electric wheelchair, taking adaptive ballet classes, and handing out playbills at her parents' dinner theater shows. Transfixed by an orchestra performance in 5th grade, Gaelynn was determined to play the cello. When her shortened limbs made playing the instrument challenging, she employed a familiar tactic: adapting. What if she held a violin upright in her wheelchair, like the world's tiniest cello?

My stroke occurred on December 10, 2021. During the hours that my mind was deteriorating, my life was sent down an inevitable pathway that would include emergency medical intervention, brain surgery, and months of therapy addressing physical and emotional health as well as speech and cognitive skills. What was not inevitable in all of this was the unique inner duality that emerged. Buddy (right brain) embraced the realm of peace and tranquility. Sir! (left brain) controlled the management of the brain: order, details, time, and knowing the feeling of being in charge.

In this tenth and final instalment, Deborah talks about her dramatic health scare, and how her fitness from triathlon saw her through. Deborah speaks honestly and openly about the challenges she experienced and how she uses her determination and resilience to get back on her feet. She also looks for new ways to continue her passion for triathlon.

Despite the incredible strain of all these challenges, Mindy manages them with amazing tenderness, persistence, and love. Far from a depressing story of misfortune, Last Nerve is as uplifting and witty as it is raw and real. It’s a testament to hope, the endurance of family, and the resilience of the human spirit.

How to Tell When We Will Die expands upon Hedva's paradigm-shifting perspective in a series of slyly subversive and razor-sharp essays that range from the theoretical to the personal―from Deborah Levy and Susan Sontag to wrestling, kink, mysticism, death, and the color yellow.

Vier Jahre lang schien die Welt um mich herum weiterzulaufen, während ich in einer unsichtbaren Blase gefangen war. Von lähmender Angst, tiefer Unsicherheit und sozialer Isolation geprägt, verließ ich kaum das Haus und kämpfte täglich gegen meine innere Stimme, die mich immer wieder zurückzog. Dieses Buch erzählt offen und ehrlich von meiner persönlichen Reise durch die Dunkelheit einer schweren psychischen Erkrankung. Es beschreibt den Schmerz des Alleinseins, die Verzweiflung, die Frage nach der eigenen Stärke – und vor allem den unerschütterlichen Willen zur Veränderung.

Up All Night not only grips listeners in unrelenting humor, but it offers a fresh voice embracing listeners with graphic injuries, tender recollections, big surprises, and love. Posing nuanced psychological questions while never losing its heart, Up All Night traces the challenges of living with undiagnosed Asperger's syndrome before the social disorder became known in 1992.

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.

In Pass the Salt, Robert Kingett invites you into his world of online dating in 2010s Chicago–a world filled with unexpected challenges, outrageous encounters, and more than a few colorful characters. As a gay man navigating not only the complexities of love but also life with disabilities, Robert’s journey is anything but ordinary.

Science writer Lorraine Boissoneault has been in pain for most of her adult life. Unable to control or make sense of her chronic illness diagnoses, she began describing the ebb and flow of her symptoms as “body weather.” At first an imaginative approach to coping with flare-ups, the phrase has become a waypoint in Lorraine’s explorations of the intimate relationship between our fragile bodies and the fragile world around us.

On t'a appris que le handicap était une faiblesse. Qu'il limitait les possibles. Qu'il condamnait à une vie en retrait. Et si c'était tout l'inverse ? Virginie Delalande est née dans le silence. On lui a prédit l'échec. Elle a choisi la vie.

Ce parcours c'est avant tout une belle histoire d'amour. Une histoire à deux qui malheureusement se termine mais accroît le désir inconditionnel de devenir père, le combat d'un homme pour connaître la paternité, y compris seul. À travers ce témoignage, Mathieu Ceschin se livre sans filtre sur ce combat, celui d'une vie, pour toucher à la paternité.