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―誰もが、けっして一人で生きていくことはできない―阿武隈山脈を遥かに眺望する小高い丘陵地「光の丘」は、東北・北海道では最初となる肢体不自由児施設誕生の地で

In Seeing Voices, Oliver Sacks turns his attention to the subject of deafness, and the result is a deeply felt portrait of a minority struggling for recognition and respect - a minority with its own rich, sometimes astonishing, culture and unique visual language, an extraordinary mode of communication that tells us much about the basis of language in hearing people as well.

INSTANT NEW YORK TIMES BESTSELLER WINNER OF THE NAUTILUS GOLD AWARD “A powerful and provocative testament to the diverse coalition of minds we’ll need to face the mounting challenges of the twenty-first century.” —Steve Silberman “An absolute eye-opener.” —Frans de Waal A landmark...

A deep dive into the spectrum of Autistic experience and the phenomenon of masked Autism, giving individuals the tools to safely uncover their true selves while broadening society’s narrow understanding of neurodiversity “A remarkable work that will stand at the forefront of the...

“I never wanted to be hearing. I said this out loud in my TED talk, and the audience went bug-eyed, struggling to process this heresy. How could anyone not want to be hearing? I wasn’t anti-hearing. I just felt my life would be simpler if everyone else were deaf.” So begins the compelling story of acclaimed TED speaker Rebecca Knill as she guides us through a life shaped by hearing loss. Throughout, Knill offers eye-opening insights into disability and celebrates the power of technology to level the playing field.

Neurodiversity is on the rise. Awareness and diagnoses have exploded in recent years, but we are still missing a wider understanding of how we got here and why. Beyond simplistic narratives of normativity and difference, this groundbreaking book exposes the very myth of the 'normal' brain as a product of intensified capitalism.

Growing Up Disabled in Australia is the fifth book in the highly acclaimed, best-selling Growing Up series. It includes interviews with prominent Australians such as Senator Jordon Steele-John and Paralympian Isis Holt.

More than 2,000 years ago, Aristotle said: "let there be a law that no deformed child shall live." This idea is alive and well today. During the past century, Supreme Court Justice Oliver Wendell Holmes Jr. argued that the United States can forcibly sterilize intellectually disabled women and philosopher Peter Singer argued for the right of parents to euthanize certain cognitively disabled infants. The Life Worth Living explores how and why such arguments persist by investigating the exclusion of and discrimination against disabled people across the history of Western moral philosophy.

It’s time to remake the world – the ground-breaking book on what steps we should all be taking for the autistic people in our lives. The modern world is built for neurotypicals: needless noise, bright flashing lights, small talk, phone calls, unspoken assumptions and unwritten rules – it...

Live your best, unashamedly unmasked Autistic life with this invaluable resource featuring tools for navigating friendships, family, work, and love, from the author of Unmasking Autism. “Unmasking for Life should be read by not only autistic people but their loved ones, to ensure they...

How can I enjoy my hot disabled body whilst dealing with internalised ableism? How can I best navigate my sex life with mobility issues or a carer? Why are queer spaces so inaccessible - and what can I do about it? Andrew Gurza is seriously hot. He's also seriously disabled. Having spent a...

This challenges abled-bodied to reflect on their attitudes and behaviors towards the special needs community. Highlighting how quickly life can change and why compassion is essential. Through real-life insights and heartfelt narrative, and encourage listeners to build bridges of love, respect and understanding.

'I heard a horrible screaming sound, like an animal being slaughtered ... then I realised it was me.' When Katie Piper was 24, her life was near perfect. Young and beautiful, she was well on her way to fulfilling her dream of becoming a model. But then she met Daniel Lynch on Facebook and her...

Blame: Death, Disability, and the Search for Justice for Guy Mitchell attempts to find meaning and justice in the tragic death of a vulnerable individual whose circle of care failed him. Dramatic nonfiction that sounds like a legal thriller, Blame resists easy answers, exposing a tangled web of negligence, indifference, and systemic failure and probing the deeper structural forces behind Guy's death. What emerges is a powerful indictment of a broken system and a strong argument that the duty to care for society's most vulnerable ultimately lies with us all.

In this deeply moving memoir, L.A. Batista recounts her incredible journey through a life filled with obstacles — family turmoil, physical challenges, an abusive marriage, and single parenthood. Despite the hardships, her story is one of unyielding strength and resilience. Beginning with her childhood in the 1960s in a neighborhood in New York City, the author recounts her family life as she dealt with an undiagnosed rare disease.

In 1963, Philip Hodges was born, the seventh of eight children, inflicted with Cerebral Palsy. Thanks to the loving devotion of their parents, who saw Philip as a gift and not a burden, the author and his siblings experienced the power of love, devotion, and acceptance that forever changed their lives.

Antonella Ferrari ha la sclerosi multipla. Sfidando giorno dopo giorno le difficoltà della malattia, è diventata attrice, ha avuto successo, ha scritto un libro in cui racconta la sua storia e che le ha permesso di entrare in contatto con tante persone che avevano bisogno di leggere le sue parole. Ma c’è un sogno che non ha potuto realizzare: diventare madre. Ogni strada, fino a qualche anno fa, sembrava essere sbarrata.

NAMED A BEST BOOK BY BOOK RIOT, AND MORE! The incredible story of an all-deaf high school football team’s triumphant climb from underdog to undefeated, their inspirational brotherhood, a fascinating portrait of deafness in America, and the indefatigable head coach who spearheaded the team...

When Ashley Shew became a self-described "hard-of-hearing chemobrained amputee with Crohn's disease and tinnitus," there was no returning to "normal." Suddenly well-meaning people called her an "inspiration" while grocery shopping or viewed her as a needy recipient of technological wizardry. Most disabled people don't want what the abled assume they want—nor are they generally asked. In vibrant prose, Shew shows how we can create better narratives and more accessible futures by drawing from the insights of the cross-disability community.

A much-needed guide to dating--from apps to hooking up, sex, long-term relationships and more--from disabled essayist and author Jessica Slice and bioethicist Caroline Cupp. Disabled people date, have casual sex, marry, and parent. Yet our romantic lives are conspicuously absent from the media...