検索キーワード： 障害者

In this fascinating story, Yahye reveals, in his own words, mesmerising incidents of resilience, exclusions and inclusions, an identity crisis, divine-connection, and an unparalleled zest for a purposeful life, all through a captivating, humorous, and candid style.

Born with a rare, incurable genetic disorder that doctors misdiagnosed until her 30s, Amy’s right leg swelled until it was 200 percent bigger than her left leg. Her peers bullied her for having an “elephant leg,” and she learned to hide her disability by wearing skirts. In an attempt to recreate her identity as a teenager, she competed in the Miss Junior American Coed Pageant, and—to her shock—she won, only to become known as “the beauty queen with the big leg”.

After years of unexplained health problems, Polly Atkin's perception of her body was rendered fluid and disjointed. When she was finally diagnosed with two chronic conditions in her thirties, she began to piece together what had been happening to her - all the misdiagnoses, the fractures, the dislocations, the bone-crushing exhaustion, the not being believed. Some of Us Just Fall combines memoir, pathography and nature writing to trace a fascinating journey through illness, a journey which led Polly to her current home in the Lake District.

This program is read by the author. An inspiring memoir of a young man who discovered he was going completely deaf just at the moment he’d fallen in love for the first time. As a child, Matt Hay didn’t know his hearing wasn’t the way everyone else processed sound—because of the...

Life is never easy, but there are times when it feels like everything is against you. Tyra Hodge grew up feeling the world's weight pressing down on her. A nagging feeling awakened, whispering how she would never amount to anything the older she got. Daunted by the increasing demands of education and her private struggles, Tyra turned away.

An inspiring story of hope, strength and courage. After doctors said there was no hope for her newborn daughter, this mother refused to give up. Despite her daughter’s severe disabilities, Lucy went on to touch many lives with her presence and became her mother’s greatest teacher.

In a Lifetime Fight: Living with Cerebral Palsy author Amanda Forry/Fino invites listeners to follow her journey towards healing and hope. After suffering a disabling accident and enduring a lifetime of abuse, Amanda is forced to rely on her own strength and courage to confront the traumas of her past and to find a path forward.

Kimberly Crowe was back for the second year in a row with a world-renowned event in honor of International Women’s Day. International Women’s Day (IWD) 2022 celebrates the tremendous efforts of women and girls around the world in shaping the future. This summit was an epic, fun, connecting, and delightful one-day virtual event in celebration of International Women’s Day, March 8, 2022. Our speakers are an amazing array of women bringing their brilliance to serve the greater good and contribute their zone of genius to the world.

Luisa L’Audace wächst als einziges behindertes Kind in ihrem Heimatdorf auf. Warum sie im Sportunterricht immer als Letzte gewählt wird, in der Pause nicht mitspielen soll und ihre Freundinnen plötzlich nicht mehr neben ihr sitzen wollen, versteht sie lange Zeit nicht. Während andere Kinder Freizeitbeschäftigungen nachgehen, verbringt Luisa viel Zeit in Krankenhäusern, bei Therapien und Spezialist*innen. Als sie mit 14 einen Rollstuhl bekommt, fühlt sie sich zum ersten Mal in ihrem Leben frei. Doch mit der neu gewonnenen Mobilität nehmen auch die Anfeindungen zu.

As a neurodivergent child in a hundred-year-old house, Zaji Cox collects grammar books, second-hand toys, and sightings of feral cats. She dances and cartwheels through self-discovery and doubt, guided by her big sister and their devoted single mother. Through short essays that evoke the abundant imagination of childhood, Plums for Months explores the challenges of growing up mixed race and low-income on the outskirts of Portland, Oregon.

Foreword by DeAndre Hopkins In this extraordinary memoir, Sabrina Greenlee, the indomitable mother of NFL sensation DeAndre Hopkins, unveils her journey of triumph over adversity—a saga of tenacity, redemption, faith, and the profound reclamation of personal power. Sabrina Greenlee was born to...

Tommy Jessop is a multi-award winning actor, theatre performer, and campaigner. Tommy has been at the vanguard of bringing awareness of the potential of people living with Down syndrome to the media, and to government. A Life Worth Living will be Tommy's story - from his journey into acting and campaigning while showing his unstoppable determination, charisma, and love for life.

Rick Werry was living the good life in beautiful Monroe, Utah. He was a young, athletic man who woke up every morning doing what he loved for work, and he had been lucky enough to marry his college sweetheart. A year after their marriage, all of that suddenly halted when an onsite construction injury nearly claimed his life.

From NFL player Steve Gleason, a powerful, inspiring memoir of love, heartbreak, resilience, family, and remarkable triumph in the face of ALS "Gleason is a symbol of resilience, hope and optimism.” —The New York Times "Steve Gleason has changed the world." –Roger Goodell, NFL...

'Love has always intrigued me, in part because I have carried for a long time a feeling that I am doing love wrong.' Michael made a name for himself on the hit show Love on the Spectrum. After his televised first dating experiences, will he complete his quest to find his queen? Chloë was always...

Eddie Ndopu was born in 1990 with Spinal Muscular Atrophy (SMA), a rare degenerative motor-neuron disease, and told that he wouldn't live beyond age five. Now, thirty-one years old and stronger than ever, he continues to celebrate each turn around the sun as an existential defiance of the odds. Gay, Black and a wheelchair user, he is now an eminent thought-leader and holds positions at two of the most important organizations on the planet. Sipping Dom Pérignon Through a Straw is Eddie's odds-obliterating story that illustrates what true leadership can look like.

The heartwarming and hilarious part-memoir, part-guide from comedian and father-of-six Ashley Blaker, on parenting, adoption and raising children with special needs. ‘A funny, irreverent and loving book’ Daily Express ‘We had such a variety of experts visiting our home, we really needed a...

Robert L. Metts was an adventurer and a disability activist that cared deeply about the lives of people with disabilities around the world. After receiving a BA in psychology from the University of California, Berkeley, Bob continued his education there to earn a PhD in economics with a focus on economic development. While in Kenya conducting research for his PhD dissertation, he had firsthand experience with the conditions disabled people faced in developing countries.

Henry Markram is the Elon Musk of neuroscience, the man behind the billion-dollar Blue Brain Project to build a supercomputer model of the brain. He has set the goal of decoding all disturbances of the mind within a generation. This quest is personal for him. The driving force behind his grand ambition has been his son Kai, who has autism. Raising Kai made Henry Markram question all that he thought he knew about neuroscience, and then inspired his groundbreaking research that would upend the conventional wisdom about autism, expressed in his now-famous theory of Intense World Syndrome.

Greg Marshall's early years were pretty bizarre. Rewind the VHS tapes (this is the nineties) and you'll see a lopsided teenager limping across a high school stage, or in a wheelchair after leg surgeries, pondering why he's crushing on half of the Utah Jazz. Add to this home video footage a mom clacking away at her newspaper column between chemos, a dad with ALS, and a cast of foulmouthed siblings. 

Macular degeneration affects over eight million people in the United States. Patients lose central vision, the ability to read fine print and recognize faces. A diagnosis doesn't mean surrendering to these challenges. Instead, understanding this medical condition will help pave the way toward a better future-for yourself or loved one.

Have you ever been told that you can’t do something, even if that something is your dream? Mohammed Yousuf’s Ascending Adversity will prove to you that you can.

A collision with a moose on a dark highway left Susan Mockler with an incomplete spinal injury, suddenly compromising her ability to walk and to care for herself. She spent months in a rehabilitation facility learning how to adjust to her new reality, and though her body partially recovered, every aspect of her life changed.

Devenir aveugle : pour Marie-Christine comme pour quiconque, cette idée est inconcevable et terrifiante. C’est pourtant la sentence que la jeune femme de 30 ans reçoit au printemps 2018 : elle ne verra plus. Jamais. Les couchers de soleil, son visage dans le miroir ou la frimousse de son fils : désormais, tout n’existera que dans sa mémoire, jusqu’au jour où ces images disparaîtront comme peau de chagrin.

Most would not expect a book about a stroke to be entertaining, but this memoir will force you to laugh through a tragedy, then cry, then laugh again. Avrel Seale was fifty, did not smoke or drink, had low blood pressure, and had hiked more than two hundred miles the year a stroke nearly ended his life. In an instant, he was teleported into the body of an old man—unbalanced, shaky, spastic, and half-paralyzed. Overnight, he was plunged into a world of brain surgeons, nurses, insurance case managers, and an abundance of therapists.

I discover a "lost" aunt, separated from our family due to racism and discrimination against the disabled. She had a mental disability due to childhood meningitis. She was taken away in 1942 when all Japanese Americans were considered the enemy and imprisoned. She then became a "ward" of the state. We believed she had died but 70 years later found her alive and living a few miles from our family farm. How did she survive? Why was she kept hidden? How did both shame and resilience empower my family to forge forward in a land that did not want them?

Hannah Daly is a pediatric occupational therapist and an advanced sensory integration practitioner who is profoundly dyslexic, dyspraxic, and has sensory processing disorder. She has multiple university degrees but still cannot read or write. In Knowing No Boundaries, she gives an honest account of living with these hidden disabilities. This book is a unique coming-of-age, feel-good memoir that strikes the balance of vulnerability and humor.

After a diagnosis of a degenerative eye disease, John Samuel’s life—and his chance at success—started to vanish. In a world systemically unequipped for accessibility, disability inclusion is often left out of conversations about diversity. For people with disabilities, it can feel impossible to adapt and thrive when you’re already set up for failure.

Run To The Fire is the exhilarating true story of the incredible life of Rick Collins. A Vietnam veteran whose body was maimed by battle, Rick returned home to extreme tragedy and loss. An unlikely superhero, he blazed a standard of endurance, faithfulness, and sacrifice to be emulated.

I don't know whether this is the story of Jeff the autistic individual, Jeff the man of God, or Jeff the medical enigma; but I do know it is the story of Jeff, my son. Jeff was so autistic, and yet not autistic at all if you used the textbook definition. He had huge sensory integration issues and appeared to be living inside of himself, but he cared so much for God and other people that their needs always came above his own. He had severe speech issues, only spoke one-word answers, but wrote beautiful papers and prayers when given the Canon communicator.

From non-verbal to radio announcer, Good Morning, Blake: Growing Up Autistic and Being Okay lays bare—from cradle to adulthood—the myriad steps Blake has taken to find his voice and rightful place in society.

New Borning: A Bronx Tale is an autobiographical poetic story and collaboration between international photojournalist Jana Hunterova and the author Emmitt H. Thrower. The book examines the activism and art of filmmaker/activist Emmitt Thrower and the developing Bronx during the years 2001-2018.

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.

From FOX News anchor and author Harris Faulkner comes a collection of powerful, true-life stories of resilience, healing, rescue, and protection. We need reminders of God’s power now more than ever. We often think about prayer as a wish list, with God as Santa Claus. The reality is that the...

In The Future Is Disabled, Leah Laksmi Piepzna-Samarasinha asks some provocative questions: What if, in the near future, the majority of people will be disabled—and what if that's not a bad thing? And what if disability justice and disabled wisdom are crucial to creating a future in which it's possible to survive fascism, climate change, and pandemics and to bring about liberation?

This is my story. After a lifetime of trying to help everyone else get their lives together, I have finally figured out how to get mine together. I am now 72 years old, semi-retired from a business I created to help young adults with autism function in the world. I live in Mexico with my loving partner. I have fulfilling relationships with my adult children and grandchildren.

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.

I am continuing with a genre of poetry that I created that I call schizoetry. It is a literary work fusing poetry with the thoughts, feelings, and perceptions of one who lives with a schizophrenic or schizoaffective disorder. I have been writing poetry since the age of 10. My poems go deep into my mind, emotions, and my spirit. They are very revealing to say the least. I wish to reach those living with this illness.

Strong Is My Middle Name is based on a true testimony on how life changed after the death of my mother. The braveness of every circumstance that God carried me through. Being strong was all I had left to endure what was ahead; and in due time, the glory of God would be revealed within me. With every mistake and disappointment, God restored me and filled the void I was missing in my life.

FINALIST FOR THE PULITZER PRIZE Named one of the best books of the year by: THE NEW YORKER THE WASHINGTON POST THE ATLANTIC NPR PUBLISHERS WEEKLY LITHUB "Fascinating...The great strength of this memoir is its voracious, humble curiosity." - The Atlantic, The 10 Best Books of...

John Cotter was thirty years old when he first began to notice a ringing in his ears. Soon the ringing became a roar inside his head. Next came partial deafness, then dizziness and vertigo that rendered him unable to walk, work, sleep, or even communicate. At a stage of life when he expected to be emerging fully into adulthood, teaching, and writing books, he found himself “crippled and dependent” and in search of care.