Disability Biography

In this candid, humorous, and insightful book, author, political science lecturer, and “Dudeist Priest” Arch Grieve provides listeners with a first-hand account of the many lessons he has learned (often the hard way) as a person living with bipolar disorder. This guidebook is a must-listen for anyone who has recently been diagnosed with bipolar disorder or knows someone who has.

This book is a reflection of a mother’s experience when her daughter, after a sudden severe headache, was diagnosed with a torn brain aneurysm and arteriovenous malformation in the cerebellum. TJ, Evie’s brother, also shares his experience.

Our aim with this narrative is to share our journey through the labyrinth of cancer treatment—the decisions we faced, the paths we chose, and, most importantly, the lessons we learned. We hope to offer guidance, support, and perhaps a sense of solidarity to others who find themselves on a similar journey. This is not your typical medical guide; it is a well-researched companion for every aspect of your cancer journey and a deeply personal account of battling cancer from the perspective of a spouse.

Always With Me is a true story about the life of Moses Macias as he grew up in and out of the hospital for twenty-one years. He was born with spina bifida and cleft lip. As a result, he would have to endure dozens of surgeries as he would fight for his life growing up. Always With Me also details other struggles of growing up disabled such as bullying, depression, suicide, medical abuse, sexual abuse, and pain of receiving medical treatment throughout his life. Despite all the trauma he endures in life, he finds his faith in God.

How a mechanic rose above poverty and chronic anxiety to build a national enterprise and found peace with himself and his past in the process. Prepare to embark on a journey of emotions. This must-listen memoir explores the resilience of the human spirit. I literally could not stop reading From Turmoil to Triumph.

I wanted to write a book to uplift mentally ill people of the harshest variety, schizophrenic or schizoaffective like I have. I wanted to tell the story of my own life, like some people see me. I am not a pitiable sad case. I am a hero who’s gone on adventures. Sometimes I was unstable, but that is not the purpose of my story.

Nujeen Mustafa ha sedici anni e soffre di una grave forma di paralisi cerebrale che l'ha costretta su una sedia a rotelle e le ha impedito di frequentare la scuola pubblica. Ma questo non l'ha fermata: ha imparato l'inglese guardando le soap opera americane trasmesse dalla tv del suo paese e nello stesso modo ha studiato storia, letteratura, scienze.

Follow the journey of Tanita Allen, a courageous Black woman confronting the challenges of Huntington's Disease. We Exist documents her harrowing two-year struggle for a diagnosis while living in a toxic NYC apartment that triggered the early onset of her condition. Learn how she wages an impossible, decade-long legal battle against those responsible, unveiling the staggering barriers faced by marginalized communities in both medical and legal systems.

My name is Christopher Miller, the view I happen to have is a view from a wheelchair. I live with spastic cerebral palsy which affects my mobility and speech. I believe that people with disabilities need to be involved in the political process. I just happen to have A View From a Seat.

My name is Joseph A. Peragine. 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.

Theirs was an unlikely life together. Sheila gave birth to Josephine on 11th May 1993 and for twenty-three years they co-existed in a loving mother-daughter relationship, but one with a difference. Josephine suffered catastrophic brain injury at birth, never spoke to Sheila, rarely smiled and was barely able to see the faces of the people who loved her.

An Unexpected Story of Hope & Perserverance: As a young child, something was wrong with Michael. He lacked basic motor skills and was unable to follow simple instructions or answer questions. Testing revealed a diagnosis of autism with a low IQ. Experts insisted that leading an independent life would be impossible for him...and school was not an option.

I am not trying to be a role model, just a possibility. There are obstacles, and people may not always treat you properly, but there is progress. My story is one of many that doesn't choose death over paralysis. It's just a story that doesn't get told often enough.

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.

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.

When Emmett de Monterey is eighteen months old, a doctor diagnoses him with cerebral palsy. Words too big for his 25-year-old artist parents and their happy, smiling baby. Growing up in South East London in the 1980s, Emmett is spat at on the street and prayed over at church. At his school for disabled children, he's told he will be expelled if the rumours are true, if he's gay; at his mainstream school, teachers refuse to schedule his classes on the ground floor, and he loses a stone from the effort of getting up the stairs.

»Ich bin blind. Na und?« Dies ist das Motto der 47jährigen Sylvia, die sich trotz so mancher Rückschläge und unerwarteter Wendungen in ihrem Leben nicht unterkriegen lässt. In ihrer Autobiographie führt sie den Leser zu den wichtigen Stationen auf ihrem bisherigen Lebensweg, beispielsweise ihr Elternhaus und verschiedene Internatsschulen. Mit großer Offenheit spricht sie über Höhen und Tiefen und wie sie damit umgegangen ist. Humorvoll und einfühlsam berichtet sie über ihre Erfahrungen in Schule, Beruf und Familie, mit Freunden und in der Liebe.

Samantha Matthews was born in Texas in 1996. Not long after her birth, she was diagnosed with cerebral palsy. As a child living with this disability, she had to learn how to overcome many obstacles in life. As the years progress, she grew in determination and resilience to live her best life. Everyone has their struggles and challenges in life. It can be difficult to get people to see the person behind a disability.

In "Gift of Life: Transforming Destinies through Organ Transplants," you'll travel on a remarkable journey of hope, bravery, and the astonishing power of human generosity. The amazing tales of people whose lives have been profoundly altered by the gift of a second chance—the gift of life itself—are revealed in this captivating book. You'll find a tapestry of stories that reinforce the profound worth of life by inspiring, challenging, and concluding.

Her Name Was Lola is the story of Trish Ryan’s triumphant recovery from a stroke that should have killed her. She had a successful career in the entertainment industry for over 30 years until May 5th, 2017, when she suffered a severe stroke that changed her life forever. Living a very fast-paced life had not prepared her for when it all came to a grinding halt. Lost and confused with no roadmap to follow, she relied on her faith to show her the way to embrace what happened and move forward.