Showing titles in People with Disabilities

For fans of rags-to-riches stories, Be There When I Return is not just about overcoming epilepsy and finding success—it is also for those who are looking for a celebration of love in its purest form. When thirty-one-year-old Michael starts to act out of character, it gets the attention of his roommate and a woman he has started dating. After denying anything is wrong with him, Michael finally decides to visit a neurologist. His life takes an unexpected turn when he receives a life-altering diagnosis of epilepsy.

Get ready to embrace your inner warrior with Kelly-Anne Kerley's real and raw story of resilience and HOPE. Dive into her empowering story, celebrating her strength and transformation—because conquering adversity needs to be showcased with laughter and tears.

After a normal, healthy, full-term pregnancy, Margaret Moore's parents Anne and Terrence were shocked as a prolapsed umbilical cord left their daughter unable to breathe on her own. Margaret, nicknamed Meg, was not expected to live through the night and began to breathe on her own by the next day—a phenomenon that medical personnel deemed a miraculous recovery. Meg came home with a physical disability Cerebral Palsy and permanent dependence on others for help with feeding, dressing, hygiene, and transfers to and from her wheelchair and walker.

"My name is Linda Buchan, and when I was 18 years old I died. It was Saturday, June 27, 1998, when my young life ended and my new life began. A life that was to be so completely different to the one that I had envisaged, the one that I had expected...." In Linda Buchan's raw and powerful memoir, she shares her journey from the terrible night when the life and future she thought lay ahead of her was shattered.

Imagine being born into a world where fitting in was never an option. Michele Sullivan, one of the most powerful women in philanthropy, was born with a rare form of dwarfism. Meaning she has spent her entire life looking up. As the first female president of the Caterpillar Foundation, she has...

“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.

What do you do when multiple sclerosis knocks you on your ass, tells you your rap career is over, and dares you to stay down? You write a new story — and this one’s real as hell. Myelin My Shoes is the raw, unfiltered, punch-in-the-gut memoir from underground hip-hop artist Robert “B-Cide” Cardillo II, who turned pain into power and built something real in a world full of fake. From rocking shows with legends to dodging shady promoters, from touring the country to being forced into a wheelchair by multiple sclerosis — this is the story of a man who refused to tap out. No ghostwriters.

Born deaf and discovering encroaching blindness at the age of 16, Anthony Lawton’s future appeared to be full of locked doors. Prejudice. Delayed education. Distorted speech. Limited sight. But when benign strangers intercede and inner gifts reveal themselves the opportunity to pursue a childhood dream of speaking and participating in mainstream society become a realisable vision. He would need to do this before the consequences of dual sensory loss would again close the doors.

At the age of thirty-one, Dave Kelly lost his eyesight to a rare disease called retinitis pigmentosa (RP). Up until then, he had lived a life like any other young man, albeit one blessed to be growing up in Liverpool during the heyday of The Beatles and Liverpool FCs win against Leeds in the 1965 FA Cup. But then, one day everything changed. Dave was faced with a choice. He could either let blindness defeat him or he could face it head-on and live as fulfilling a life as he possibly could.

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.

Starting at the age of 12, Derek's life began to get much more complicated. An internal struggle was about to take hold. Its grip would cause unimaginable anxiety. The normal thoughts and feelings he had prior were a distant memory. This had to be dealt with using irrational methods. Over time he had to manage and cope the best way he could. This is a true account of one Northwest man's experiences living with the mental disorder known as OCD (obsessive-compulsive disorder).

Darkness—that’s what Bozena Gasior remembers feeling when she first heard her two-year-old son’s autism diagnosis. What followed was a cacophony of despair and cries, not knowing what to do, say, or feel. It was the day she thought that part of her son’s life had died. But one eventful day some four years later, his fingers touched the piano keys for the first time, and she felt something—a glimmer of light shining down, illuminating her home and family.

Barbara Melvin has a secret to her success: her five Ps. And never were they more important than the day she woke up in her Naples, Florida home, blind. In the blink of an eye, life changed.

Lorsqu'on rencontre Martin pour la première fois, ce qui frappe immédiatement, c'est son sourire charmeur, son enthousiasme, son oeil qui pétille, son aisance à l'oral et ses idées qui fusent dans tous les sens. Son fauteuil, on n'y pense même pas. On ne le voit pas. C'est tout juste si l'on remarque que ses doigts, qui paraissent pourtant si agiles, sont inertes, tant Martin a de choses à partager, d'anecdotes à raconter et de montagnes à déplacer. Pourtant, Martin est tétraplégique.

Outlaw Patients is a raw, darkly funny, and fiercely honest memoir about trying to survive in a system that wasn’t built to help. Medical marijuana patient and longtime activist Russell Barth takes listeners inside the chaotic, painful, often absurd world of Canadian cannabis policy — and the strange place where medicine, bureaucracy, and rebellion overlap.

When I was six years old, I started wearing glasses. My view of my low vision quickly changed when I was twenty years old and found out that my brother had suddenly gone blind. He was told that he was suffering from Retinitis Pigmentosa (RP), a disorder that slowly destroys the pigment cells in the eyes. So far, there are no known cures. At the tender age of twenty-one, I was also diagnosed with RP. Since then, I have been slowly going blind, not knowing when my world would finally fade away forever. Battling against such a crippling disease led me through a labyrinth of challenges.

At the age of 30, Jake found himself hospitalized, grappling with the weight of anxiety, depression, and paranoia. Soon, he received the life-altering diagnosis of schizophrenia. In this intimate and illuminating book, you are invited into Jake's world, a world he shares with his mother, Laurette, through alternating chapters.

Kevin’s life was forever changed on a random Wednesday when he was just 20 years old. An aspiring musician at the time, he was planning to attend music school and pursue his dream of becoming a composer. A stroke dismantled every plan and everything in his life. In Taken By Surprise, Kevin chronicles his battles with the stroke. After a risky brain surgery, he was in a coma for nearly a month and spent six weeks in an acute rehab facility to learn how to walk and talk all over again.

Le destin de Simone s’est écrit le jour de sa naissance. Son premier cri, elle le pousse en partie à cause d’un arrachement du plexus brachial qui paralyse son bras droit. Comme dans 80 % des situations, son handicap est invisible. Pourtant, à force de volonté et de courage elle embrasse une carrière de handballeuse, jusqu’à atteindre le très haut niveau.

DJ is the eldest daughter of four kids. Her Mom was born blind and raised her and her siblings. When DJ was 10 years old her mom’s health started to have complications. When her mom was in her 50s, she went through another health situation. She shares what it was like to start taking care of her mom. How does it work for a daughter to care for her mother?

As an adult, DJ has a son born with a congenital heart defect. She uses the things she learned while caring for her mother to care for her son. Learn how God has been the strong hold for this family through the many health trials they have gone through. This book asks the question: will you use what God is doing in your life for good?