Disability Memoir

Left partially paralysed below the rib cage by polio, Anne Wafula Strike was forced to flee her native Kenyan village, moving across the country with her family. After overcoming additional adversity, including the loss of her mother and ableist prejudice, Anne moved to the UK, where she discovered her talent for wheelchair racing. The first East African to compete in her sport, representing Kenya in the 2004 Paralympics before joining Paralympics GB, Anne is now a fierce advocate for the promotion of the games around the world, and a champion of disabled rights.

Sumérgete en la extraordinaria vida de Gerardo Schmedling, un hombre cuyo poder espiritual inquebrantable desafió las adversidades de la parálisis de Guillain-Barré en su juventud y las secuelas que afectaron su movilidad de por vida. Este relato, narrado por su prima María Mercedes Olivares Schmedling, conocida como Mechas, quien compartió con él desde su infancia, revela cómo Gerardo se convirtió en el arquitecto de un movimiento global de transformación personal y social.

Our aim with this narrative is to share our journey through the labyrinth of cancer treatment—the decisions we faced, the paths we chose, and, most importantly, the lessons we learned. We hope to offer guidance, support, and perhaps a sense of solidarity to others who find themselves on a similar journey. This is not your typical medical guide; it is a well-researched companion for every aspect of your cancer journey and a deeply personal account of battling cancer from the perspective of a spouse.

He grew up, he says, at "belt-buckle level" and stayed there until Kevan's beloved posse decided to leave his wheelchair at the Atlanta airport, board a plane for France, and have his friends carry him around Europe to accomplish their dream to see the world together! Kevan's beloved posse traveled to Paris, England, and Ireland, where, in the climax of their adventure, they scale 600 feet up to the 1,400-year-old monastic fortress of Skellig Michael.

Der Wunsch, den Jakobsweg zu wandern und einfach mal rauszukommen, ist für viele Menschen ein Traum - egal, ob man gesund, stark und ausdauernd ist. Auch Menschen mit Behinderung gehen diesen Weg, um ihre Grenzen auszutesten, um auf ein Wunder zu hoffen oder vielleicht, um mal etwas anderes zu erleben. Genau das will ich auch. Etwas Neues sehen und hören - auch als Nichtsehender und Nichthörender, denn ich bin taubblind. Ich möchte dich auf meine Reise mitnehmen. Hier in meinem Buch kannst du mich begleiten.

Frederick Moore spent his 1950s Minneapolis childhood obsessively teaching himself guitar and writing songs. In the 1960s, his bands Skogie and the Flaming Pachucos reached local stardom. After, they put everything they had into their cars and caravanned to Los Angeles. From a garage in suburban Arleta, they evolved Skogie into a new band called The Kats. In the 1980s, The Kats sold out every major club in Los Angeles.

The S Word is the raw and compelling true story of a girl coming of age raised by a mother with a mental illness, and who nearly suffocates in the silence she was taught to value above all else - until she finally finds the strength to break free of the secrets binding her and save herself. The S Word is a book for anyone who may be keeping secrets...for children too little to know they warrant a voice...for teenagers too confused to think they have a choice...for adults too overwhelmed to do what’s right.

Her Name Was Lola is the story of Trish Ryan’s triumphant recovery from a stroke that should have killed her. She had a successful career in the entertainment industry for over 30 years until May 5th, 2017, when she suffered a severe stroke that changed her life forever. Living a very fast-paced life had not prepared her for when it all came to a grinding halt. Lost and confused with no roadmap to follow, she relied on her faith to show her the way to embrace what happened and move forward.

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.

In October of 2008, I was airlifted to Erlanger Hospital in Chattanooga, TN, after a head-on collision with an SUV while riding a motorcycle. When I woke up, I was told I would never walk again or have full use of my hands. Seventy-eight screws, 13 plates, 25 units of blood, and more than 400 stitches and staples later, I became very familiar with physical pain and haven’t had a pain-free day since. That physical battle was harder than I could even begin to explain, but it doesn’t really come close to the one that I went through inside of myself over the years that followed.

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.

Lillian was a college freshman, a promising theater major facing the challenge of Stargardt’s disease, a condition that was causing her to go blind. When, in the fall of 2009, Lillian became sick, she assured her parents it was just the flu. Four days later she was in the university hospital, relying on a machine to breathe for her. Based on her father’s journal, this memoir describes what it’s like to live through a parent’s worst nightmare, conveying the heart-wrenching ups and downs of Lillian’s time in the hospital.

Kamata's adventures with her teen—who happens to be deaf, with cerebral palsy, and in a wheelchair—through subterranean Tennessee, to the islands of Japan, and to the top of the Eiffel Tower ultimately lead to a daughter's increasing independence, a mother letting go of expectations, and advocacy for travel which prohibits discrimination.

Learning disabilities (LD) are a root cause of major problems in our society. Vast numbers of youngsters are not receiving appropriate education. Nancy Lelewer’s story began when even less was known about learning disabilities than is known today. In a gripping and fast-moving narrative style, this audiobook brings home the fact that LD persons need to receive instruction via different routes and the earlier the better.

I wrote this book because I wanted the world to know the story of my special needs son Lloyd C. Darby lll. Affectionately known as DJ, which stands for Darby Junior. When people triumph over their circumstances as my wife and I have, there are usually hidden lessons others can benefit from contained within the events. However, if we don’t share our stories with the world, no one will ever hear about them.

Hall is authentic, transparent, and raw as she shares the many facets of her dynamic life and colorful personality. The chapters are like peeling an onion as Hall deftly delivers the most dismal times of her life. Listeners will experience so many emotions but will ultimately cheer for Hall’s escape, redemption, and power to rebuild a successful life. She credits her beloved 93-year-old grandmother's unconditional love and wisdom for giving her the endurance and strength to overcome all that life has dealt her.

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.

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.

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.

私たちは本当に「見て」いるのか?触れて、聴いて、初めてわかる、この社会のかたち。時に鋭く、そしてあたたかく。ユーモアに満ちた随想集。