検索キーワード： 障害者

An upcoming book to be published by Penguin Random House.

Lachi is an award-winning musician and leader who awakens the world to this truth: Disability has long shaped our culture and is an identity worth brazenly celebrating. In this book, Lachi welcomes listeners into the vibrant world of Disability Culture, centering identity, innovation, and unapologetic pride.

Discover the untold story behind one of Kathleen Norris's deeply personal relationships in Rebecca Sue. Best known for her insightful and poignant reflections on faith and life, Norris steps into uncharted territory by sharing an intimate memoir exploring the life of her younger sister Becky. Born with perinatal hypoxia, Becky's life was shaped by physical and mental disabilities, yet her spirit and resilience illuminate the hidden power of faith, family, and love.

Rachel Kolb was born profoundly deaf the same year that the Americans with Disabilities Act (ADA) was passed, and she grew up as part of the first generation of deaf people with legal rights to accessibility services. Still, from a young age, she contorted herself to expectations set by a world that prioritizes hearing people. Now in Articulate, Kolb blends personal narrative with cultural commentary to explore the different layers of deafness, language, and voice.

The forms of intimacy and care that we’ve been sold are woefully inadequate and problematic. In a world that treats those who are sick and traumatized as problems in need of a cure, nonbinary writer, artist, educator, and Instagram creator Margeaux Feldman offers a different story. Trauma, which all too often manifests as chronic illness, tells us that there is something deeply wrong with the world we live in. A world that promotes individualism, fractures us from community through violence and systemic oppression, and leaves us traumatized. That is what we need to cure.

Raymond Antrobus was first diagnosed as deaf at the age of six. He discovered he had missing sounds—bird calls, whistles, kettles, alarms. Teachers thought he was slow and disruptive, some didn't believe he was deaf at all. The Quiet Ear tells the story of Raymond's upbringing at the intersection of race and disability. Growing up in East London to an English mother and Jamaican father, educated in both mainstream and deaf schooling systems, Raymond explores the shame of miscommunication, the joy of finding community and shines a light on the decline of deaf education in Britain.

From the remarkable man whose life inspired the heartstopping film, ‘I Swear’, a book that offers extraordinary insight into what it’s like to live with a severe form of Tourette’s Syndrome: a fascinating, complex condition that’s more common than most of us think (1 in 100 schoolchildren have the condition), and yet is chronically misunderstood.

Raymond Antrobus was first diagnosed as deaf at the age of six. He discovered he had missing sounds—bird calls, whistles, kettles, alarms. Teachers thought he was slow and disruptive, some didn’t believe he was deaf at all. The Quiet Ear tells the story of Antrobus’s upbringing at the intersection of race and disability. Growing up in East London to an English mother and Jamaican father, educated in both mainstream and deaf schooling systems, Antrobus explores the shame of miscommunication, the joy of finding community, and shines a light on deaf education.

Time in nature supports our well-being. For people who are neurodivergent, it can also stimulate our senses, feed our curiosity and help us find others who share our deep passions. But why do natural environments have such profound effects? If children with autism, ADHD and other neurodivergences spend more time outdoors, could it improve their educational experiences and outcomes? And if they nurture nature connections into adulthood, could this form the roots of their identities?

A two-week vacation to the Florida Keys meant Mary and Jameson Sr. could share the beauty of their favorite turquoise-blue waters with their four children. On that serene day at Looe Key Reef, after they finished lunch on the boat, their oldest, ten-year-old Jameson Jr., was swimming among the marine life, capturing breathtaking footage of a sea turtle. Until a massive bull shark attacked.

Twenty-three-year-old Ardra Shephard is sleeping with the wrong guy, living in a crappy apartment, and spending money she doesn't have on designer shoes, boozy brunches, and weekends in NYC. Making mistakes while you figure stuff out is what your twenties are all about. Then a doctor tells Ardra she has MS, and those two letters split her life into a Before and After.

After being diagnosed with muscular dystrophy, Melissa Haugen felt alone. In an effort to make others feel seen, she vulnerably shares her personal story of living with muscular dystrophy.

After a normal, healthy, full-term pregnancy, Margaret Moore's parents Anne and Terrence were shocked as a prolapsed umbilical cord left their daughter unable to breathe on her own. Margaret, nicknamed Meg, was not expected to live through the night and began to breathe on her own by the next day—a phenomenon that medical personnel deemed a miraculous recovery. Meg came home with a physical disability Cerebral Palsy and permanent dependence on others for help with feeding, dressing, hygiene, and transfers to and from her wheelchair and walker.

Athena Stevens has never learned the name of the doctor whose lack of intervention at her birth lead to her cerebral palsy, but she feels the consequences of his actions – and inaction – every day. The factor observed first and foremost in her life will forever be the effects of what other people have done to her, rather than her accomplishments. And yet, she was groomed to believe that she would overcome any force that stood in her way.

Growing up with Autism is hard enough. Growing up with Autism when you're a little gay weirdo is almost impossible. Greatest Hits of my Childhood Trauma is the story of a boy fighting to exist in a world that would rather throw him away. From overly religious mothers to prison sentences, drug overdoses, psychiatric facilities, bizarre sexual encounters, and queer high school romance, this tale of 90s middle America is heartbreaking, hilarious, and hard to put down. Alex Dark takes us through the darkest parts of his life with a charm that will keep you coming back for more.

This is the very personal and frank account of A.W.J. Pilgrim’s battle with schizophrenia, in the context of his whole life story. He is a Londoner, dad and talented prolific artist painter and author. Learn how his illness progressed, how he struggled, his personal thoughts about it, detailed accounts of being sectioned, effects of medications, psychosis, hallucinations & delusions. The story not all sad, he has had some good luck too, and still has dreams. Learn how he has put his schizophrenia into remission.

For fans of rags-to-riches stories, Be There When I Return is not just about overcoming epilepsy and finding success—it is also for those who are looking for a celebration of love in its purest form. When thirty-one-year-old Michael starts to act out of character, it gets the attention of his roommate and a woman he has started dating. After denying anything is wrong with him, Michael finally decides to visit a neurologist. His life takes an unexpected turn when he receives a life-altering diagnosis of epilepsy.

We all face obstacles that threaten to hold us back. For Robert Paylor, his paralysis wasn’t a metaphor. In the biggest game of his life, competing for the collegiate rugby national championship, Robert suffered a catastrophic spinal cord injury that left him paralyzed from the neck down. Doctors told him he’d never walk or move his hands again. But Robert refused to accept that fate.

Jason Dunkerley’s Visions of Hope: Running Towards My Own Truth is the inspiring autobiography of a distinguished Canadian middle-distance runner, who has been blind from birth due to a congenital eye condition. He achieved international acclaim as a five-time Paralympic medalist and world champion.

When Roger Rasmussen was diagnosed with prostate cancer in 2019, he did what most patients do: listened carefully, weighed his options, and tried to make peace with the life-altering decisions ahead. Then he heard about Joe Tippens' story, which led him down a rabbit hole of research into something unexpected—a compound called fenbendazole with curious case reports and a growing collection of personal accounts.