検索キーワード： 障害者

This book chronicles the journey of Eritrean-born Joseph Woldu. As a child refugee, he found himself having to adapt to changes of place, language, and customs; then as a man forced to relearn much of the same after involvement in a disastrous accident two days before the 9/11 terrorist attacks. What makes Joseph's story so incredible is not that he survived change and tragedy, but how he continually found the strength to improve himself and his circumstances. His story reflects the importance good relationships play in our lives.

On Halloween day 1990, Sterling Krysler—husband, father, pilot, newly arrived in Hawai'i—suffered a catastrophic spinal cord injury while body surfing at a local beach. Ever the optimist, Sterling accepted the life-changing injury becoming advocate and inspiration to many in the "disability community." This is a family-centered story brimming with love, joy, and humor. This is his story—before and after.

Before becoming the actor, producer, advocate, and model that people know today, Nyle DiMarco was half of a pair of Deaf twins born to a multi-generational Deaf family in Queens, New York. At the hospital one day after he was born, Nyle “failed” his first test—a hearing test—to the joy and excitement of his parents.

We were walking this journey together, yet alone. Two siblings from a close-knit, boisterous family of six. There is nothing like the camaraderie of family to give you the determination to persevere in spite of any obstacle. We were overwhelmed by the disease of multiple sclerosis as well as other autoimmune diseases. Our outward appearance of healthiness was deceiving. Unbeknownst to us, the disease of multiple sclerosis would eventually consume mobility, sight, memory, fine motor skills, speech, and so much more.

They say if you want to make God smile, tell him you have a plan. Dwight’s plan was to live his dream, teach math, coach football, and build a comfortable life for himself. Fate had other things in store for him. The story of Dwight’s physical and emotional journey from life as an able-bodied young man chasing his dreams only to have his world turned upside down by the thoughtless act of a 71-year-old drunk driver.

So begins Chloé Cooper Jones’s bold, revealing account of moving through the world in a body that looks different than most. Jones learned early on to factor “pain calculations” into every plan, every situation. Born with a rare congenital condition called sacral agenesis which affects both her stature and gait, her pain is physical. But there is also the pain of being judged and pitied for her appearance, of being dismissed as “less than.”

In No Bad Days, JT details the incredible story of how he overcame what seemed like insurmountable odds and shares the many invaluable lessons he has learned throughout his life in the hope that others might reach their full potential. These lessons include how to: find your tribe, pull off the label, stretch yourself, listen to others, and learn to fall. JT’s improbable life story is evidence that regardless of the mental and physical challenges you might face, you can defy the odds to create the life you want and accomplish the things you’ve only dreamed about.

Stoney McGurrin, in his debut book, brings us on the adventure of his lifetime. Having spent months in the hospital as a four-year-old, where he almost lost his arm, only to have it saved by a famous French surgeon Dr. Chance, he left Leitrim as a teenager on ship across the Atlantic to New York City. The stories are exciting, sad, happy, and true; from 1941 to the present, from pencil to paper.

Look at It This Way answers questions we all may have been reluctant to ask, it gives us a glimpse into what blind people experience living in a sighted world, and it breaks through barriers that may cause people to think that differences equate to superiority or inferiority.

As a result of complications during the birthing process, Amanda was born with cerebral palsy. This book recounts the trauma she experienced as a child, enduring physical, mental, sexual, and emotional abuse from her family, and having a mother who cannot tolerate her cerebral palsy. Amanda found comfort and solace in her grandmother, her '"Gragwa", throughout her childhood. Amanda exposes the naked truth of life with cerebral palsy as she deals with growing up and various relationship issues, friendship issues, loss, and many other things.

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.

In 2012, combat engineer Curtis McGrath was serving in the Australian army in Afghanistan when, in the line of duty, he stepped on a mine. Seriously injured but still conscious and aware he'd bleed out and die within minutes, McGrath, as the unit's chief first-aid officer, directed his comrades to apply tourniquets and administer an IV and morphine. Then, as he was stretchered to a helicopter, fearing he would never see his family again, he joked that he planned to become a Paralympian.

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."

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.