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Love for a Deaf Rebel introduces listeners to a vivacious Canadian woman who was born into a silent world and with the foundation for schizophrenia. With pathos and nostalgia, the author recounts his roller-coaster ride with Pearl, a vivacious deaf maverick, who, unknown to him, had paranoid schizophrenia. We follow their encounters through actual notes written before Derrick learns sign language; we go on their motorcycle ride to Mexico and Guatemala; we watch as the happy couple moves to Bowen Island, a British Columbia community with just three paved roads.

Bill Rush lived with a significant disability of quadriplegic cerebral palsy. He did not have use of his arms, hands, or voice. Society’s prejudices proved to be a greater obstacle than his disability in attaining his first life goal of completing college. Rush chronicled his extraordinary life from childhood until graduation from the University of Nebraska - Lincoln in Journey Out of Silence, first published in 1986. This second edition brings back into print Bill's original chronicle. It also contains an introduction to Our Life Our Way, the sequel.

If you're skeptical about changing society's discriminatory treatment of people with dwarfism and other disabilities, Van Etten offers hope with these words: "Advocacy makes change possible when people call out what is wrong, care enough to stand up for what is right, commit to the cause for as long as it takes, and have confidence in God's power to change hearts". Van Etten repeatedly demonstrates the power of advocacy in this audiobook.

For 20 years, Lisa Murphy, Jeff Murphy, and a group of volunteers traveled the world with the Mobility Project, delivering mobility to the poorest people on the planet. They helped tens of thousands of disabled poor to gain mobility and hope. The disabled received wheelchairs, walkers, and crutches from the United States, items they never would have been able to afford. Like Simon of Cyrene, we helped people carry their cross of disability. From the hot tropical jungles of Costa Rica, Thailand, and São Tomé to the deserts of Afghanistan, the disabled poor got a new chance at life.

I realized, at age 70, that I had no memory of being inside my home, where I grew up, or ever being inside a school classroom. I began to write then, and have continued over the last 24 years, as one painful memory after another was slowly revealed. Recently I figured out what had happened to my mother, and therefore to me. Two more major insights totally freed me. I could then finish Missing Pieces.

When a tragic accident crushes her dreams, can a young woman fight to thrive once again? As a teen growing up in the '80s, Jenny Smith loved life. But, when a spinal cord injury paralyzed her from the chest down, her days of gymnastics and playing music came to an agonizing end. Completely reliant on others for her most basic needs, privacy and independence became things of the past. Refusing to give up, Jenny struggled along the exhausting, painful, and endless road to living as a quadriplegic.

Myrna was a vivacious and active youth, who, at the age of 14, was paralyzed from her waist down by polio in 1951. This is an inspiring story of how faith, positive attitude, persistence, and the unconditional love and support of family and a community led to her miraculous recovery from polio.

Everything happens for a reason; I truly believe writing these words was one of the primary purposes of my life. Father God gave me this disability - I’m just trying to make the most out of it. This is not your typical autobiography or memoir. I’m sharing my life experiences as more of a commentary on humanity as a whole. I do my best to sprinkle bits of comedy throughout the composition so it feels more like a conversation between friends than me just talking at you.

Throughout our life, we all have different challenges, how can we allow these obstacles to facilitate growth and expansion, not contraction or fear? Cyrina Bullard PharmD, the author, will take you on a journey that begins with a lightning strike, jolting her to the ground. This was the first of the trilogy of nearly fatal episodes in her life. Personally revealing, authentic, and vulnerable, Cyrina shares some challenging details of her life, with the intention of inspiring you to enjoy your moments.

At 90 years old and blind, Lorraine decided there was never a better time to get started as a writer. Juggling career, marriage, motherhood, and staying a vibrant senior demands constant skill upgrading. Lorraine’s early childhood development expertise, for instance, was perfected during her 81 months of pregnancy. As a first generation of Russian immigrant parents, Lorraine’s daily walk with God is a testament to her belief and love-filled life. She says, “Hope is not a plan, but it is a promise that’s given when faith and belief become action.”

A Michele La Pusata, dodici anni fa, è stata diagnosticata la Sclerosi laterale amiotrofica, meglio conosciuta come SLA. Prima, la sua era una vita più che normale, tra figli, lavoro e piccole incombenze, poi non lo è stata più. Non si mette mai in conto di affrontare una malattia lenta e invalidante come questa e infatti nessuno è preparato.

Spoke by Spoke takes the listener on one woman's journey to reinvent herself following a hit-and-run accident which left her back broken and her bike crumpled by a speeding motor vehicle. The stories Terry shares will take you from the depths of despair and the edges of darkness to profound realizations about what we are all capable of. Terry's perseverance and resilience - fueled by her amazing spirit - show us that whatever hand we're dealt, we always have the choice to live a wholehearted life.

A profoundly beautiful memoir about disability, difference, and living as a vulnerable body. Jan Grue had just become a father when he inherited a stack of his childhood medical records. Following a diagnosis of spinal muscular atrophy at the age of three, the raft of doctors' notes, clinical descriptions and case histories defined his body as defective and his future as bleak and limited. They conjured a childhood nothing like the one he remembered, that failed to anticipate the life he lived now. "I Live a Life Like Yours" is Grue's beautiful, groundbreaking search for a literary language that could better tell his story.

Essere una donna disabile in un mondo in cui l'immagine femminile appare sempre patinata e perfetta non è facile, ma Antonella Ferrari, attrice e ballerina, malata di sclerosi multipla, non si è mai arresa tanto da diventare un punto di riferimento, una fonte di ispirazione per tante persone meno fortunate. "Mi sono beccata tantissime porte in faccia, tantissime delusioni ma dovevo andare avanti anche per tutti quelli che vivono bloccati per colpa di una malattia."

In this unique and exhilarating autobiography, Allan Jones - Canada’s first blind diplomat - vividly describes how an untreatable eye disease slowly decimated his visual world, most challengingly during his postings in Tokyo and New Delhi, and how he discovered and took to heart the revelatory Indian philosophy that changed his life.

Type 1 diabetic, fitness fanatic, dancing queen, Canasta champion; only some of the tags used to describe Colleen Ashby. Daughter, sister to five brothers, wife, and mother of three sons further define Colleen. Add to that, she is a heart transplant recipient who is now visually impaired, and you realize there is much more to learn.

Growing up with a learning disability, Josh was often told what he wouldn't be able to do. Fortunately, he did not listen. With the help of some wonderful teachers and friends, Josh found that he can do more than others ever predicted. Follow Josh on his journey through school, work, and his long-time participation in Special Olympics. Watch him confront challenges, overcome obstacles, and keep moving forward. This inspiring story will have you rooting for Josh from start to finish.

Max Toper isn't normal. His teacher segregates him at the back of the class, away from his peers. Other children make friends, yet he can't. He's told he has autism, a condition that seems to bring disaster after disaster, with no chance of achievement. But not all is hopeless. Change comes when he discovers his calling as a guild leader in the virtual world of Galactic Conquest, a place where he is respected and powerful. But can the digital world stop reality seeping in, or prevent him from addressing his demons?

This inspiring autobiography by Helen Keller is an account of her life from her family history up to her last years of college, supplemented by her personal letters from age 7 to 21. This edition includes letters and reports contributed by her teacher, Anne Sullivan, and the editor, John Albert Macy.

I was born living the American dream. I had a mother and father who loved me. An older sister who cared for me. A beautiful house on a lake and extended family close by. But life has this way of flipping you inside out. By age two, we'd lost our home. By age six, my mother had died. For the next five years, we moved from place to place, crisscrossing the country.