Showing titles in People with Disabilities

"It's A God Thing," is a collection of stories illuminating the blessings that enrich our lives. From enduring friendships to the profound moments of divine intervention, this book captures faith in action. The Stories: The Blessing of Friendship: The unbreakable bonds that sustain us through life's challenges. The Blessing Challenge: Experience the blessings in everyday life. Pawprints on Our Hearts: The unique and touching connections we share with our pets, who truly are family. Special Olympics, Special Memories: The incredible spirit and determination of athletes who redefine what it ...

In this audiobook, you will catch intimate glimpses of how manic depression or bipolar disorder affects not only those diagnosed but the entire support structure around them. You'll find inspiration and hope that our fractured mental health system still holds opportunities for healing and unearthing resilience. In Hard Pill to Swallow: My Manic Memoir, Logan carries you through his struggles with his identity as a gay/bisexual man coming to terms with addiction while simultaneously battling bipolar disorder.

David Paterson overcame severe disability and racial prejudice to become a state senator, lieutenant governor, and - unexpectedly - governor of New York. Paterson was the first and only blind governor - other than a man who held the title for 11 days in 1975 - and the fourth person of African descent to hold the office of governor in American history. Paterson may also be the only governor in history to have been arrested outside the governor's office prior to his service.

Esta autobiografía cubre muchas facetas de la experiencia humana: raza, salud, discapacidad, religión, pobreza, inmigración, acceso a la atención médica, educación, derechos de las personas con discapacidades, aborto espontáneo, adopción y mucho más.

In 2009 I lived in Highlands, North Carolina, before I became resolute to graduate or ever even started at Berea College. My internship with three other women, under the stewardship of a Unitarian nonprofit retreat center, was a time of questioning and growing more than any other time of my life. It also encouraged a raw, unique style of writing, influenced by the old-growth dwarf oak forest surrounding us and a certain Meditation Rock where we loved to sit and overlook the rolling mountain.

The GIs called her Joey. Hundreds owed their lives to the tiny Filipina who stashed explosives in spare tires, tracked Japanese troop movements, and smuggled maps of fortifications across enemy lines. As the Battle of Manila raged, Josefina Guerrero walked through gunfire to bandage wounds and close the eyes of the dead. Her valor earned her the Medal of Freedom, but what made her a good spy was also destroying her: leprosy, which so horrified the Japanese they refused to search her.

Living in the Belgian Congo with her husband in the 1960s, Fran’s mother became pregnant with a daughter. However, right after she gave birth in the hospital, she felt strange. Unbeknownst to anyone, another daughter was on the way, but before anybody responded, an hour had passed. Because of the delay, Fran was born with cerebral palsy. Growing up with her siblings in Africa, Fran always felt different. When everyone else was playing and having fun, she would watch and wish she could join in.

When Ellie Goldstein was first diagnosed with Down Syndrome, her mother was soon told that her new-born would amount to nothing. For 21 years and counting, Ellie Goldstein has been defying the odds and overcoming every hardship thrown at her. Told she wouldn't walk, Ellie has danced on mainstages. Told she wouldn't learn, she has gained a college education. And told not to dream, Ellie has gone on to become the first model with Down Syndrome to be photographed for Gucci and continues to change the face of fashion from the inside out in countless international campaigns.

Blinded at age three, Mike May defied expectations by breaking world records in downhill speed skiing, joining the CIA, and becoming a successful inventor, entrepreneur, and family man. He had never yearned for vision. Then, in 1999, a chance encounter brought startling news: a revolutionary stem cell transplant surgery could restore May's vision.

You struggle with your disability. You're tired of being counted out of life. Are you frustrated because you feel, or have been told, you can't be 100% healthy with your disability? It's time for a change! It's time to prove everyone (including your doctors) wrong! Author and certified personal trainer Tony Jacobsen, who has Osteogenesis Imperfecta (Brittle Bones Disease), has transformed his entire life and now shares the formula to empower other people with disabilities.

From the Periphery consists of more than 30 first-person narratives of everyday people who describe what it's like to be treated differently by society because of their disabilities. The stories are raw and painful, but also surprisingly funny and deeply inspiring. The oral histories describe anger, independence, bigotry, solidarity, and love - in the family, at school, and at the workplace. From the Periphery will become a classic collection that increases understanding of the lived experiences of people with disabilities.

Buzz Bissinger’s twins were born three minutes—and a world—apart. Gerry, the older one, is a graduate student at Penn, preparing to become a teacher. His brother Zach has spent his life attending special schools. He’ll never drive a car, or kiss a girl, or live by himself. He is a savant, challenged by serious intellectual deficits but also blessed with rare talents: an astonishing memory, a dazzling knack for navigation, and a reflexive honesty that can make him both socially awkward and surprisingly wise.

Dan McSkimming was a Deputy for 18 years and on the SWAT team (SET - Special Enforcement Team) for 13 years— all with the Santa Barbara Sheriff’s Office. A normal adjustment of his rifle led to a visit to a chiropractor which would change his life forever. A stroke sent him to Cottage Hospital—the same Hospital of his birth. At age 43, Dan had to learn to live all over again—how to talk, eat, communicate, love… This is the true story of a shocking tragedy and trauma, the fear, despair, and triumph of a first responder, in his own words.

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.

A late bloomer’s coming-of-age memoir asks how does one accept and free themselves from visible and invisible disabilities and still retain their sense of connection and humor? Nothing Special is a disarmingly candid tale of two sisters growing up in the 1970s in rural Connecticut. Older sister Chris, who has Down syndrome, is an extrovert, while the author, her younger, typically developing sister, shoulders the burdens and grief of her parents.

Bonner Paddock grew up just wanting to be ordinary. Diagnosed with cerebral palsy at age eleven, he guarded the truth about his health, building a normal life and keeping his secret from everyone—most of all himself—for the next eighteen years. But the sudden death of a friend’s young son due to cerebral palsy forced Bonner to reevaluate who he was and spurred him to pursue one breathtaking experience after another.

Graham Hale Gardner died before turning 23 and never learned to walk or speak due to severe cerebral palsy complicated by epilepsy. Yet he left a legacy of love and compassion that deeply moved scores of people from widely different backgrounds. Graham’s story, written through the eyes of his father, speaks of the enormous legacy left by a boy who never spoke. A story that raises provocative questions about the “invisible lines of connection” that make us human.

An unflinching and luminous memoir that explores a father’s philosophical transformation when he must reconsider the questions what makes us human? and whose life is worth living? Before becoming a father, Chris Gabbard was a fast-track academic finishing his doctoral dissertation at Stanford. A disciple of Enlightenment thinkers, he was a devotee of reason, believed in the reliability of science, and lived by the dictum that an unexamined life is not worth living. That is, until his son August was born.

Shortly after his daughter, Leontine, was born, Christian Donlan's world shifted an inch to the left. He started to miss light switches and door handles when reaching for them. He would injure himself in a hundred stupid ways every day. First playful and then maddening, these strange experiences were the early symptoms of multiple sclerosis, an incurable and degenerative neurological disease.

Navigating a Life with Disability? Raising a Special Needs (or whatever you're calling, today) Child? Read This: A Pathway Guide Through Adversity with Quiet Candor and Humor (because you're gonna need it!)... Disability: An Anecdotal Field Guide for the Rest of Us offers firsthand wisdom and practical tips for navigating life with a disability. Drawing on her own experiences as a woman with muscular dystrophy, Tracee Garner covers topics from advocacy to employment, mental health to emergency preparedness. Written in an engaging conversational tone, this “field guide” shares key ...