Social Disabilities

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.

Lucy Edwards is a UK-based blind broadcaster, content creator, Pantene Ambassador and disability activist. At only 17 her world went to black. In an instant Lucy lost her eyesight due to a rare condition called Incontinentia Pigmenti. She had to learn how to navigate her life all over again, the beginning of an extraordinary journey to find self-acceptance and happiness. Lucy took to the internet and started to upload her experiences. Through sharing her day-to-day routine in her viral 'How does a blind girl?' video series, Lucy's story gripped the nation.

Sally Hobart Alexander continues the story of her journey into blindness in this uplifting tale of a life rebuilt and love renewed. Suzanne Toren’s perceptive narration perfectly expresses the emotions of Sally’s sometimes fun, often arduous, and always interesting journey. Also available is Taking Hold, My Journey Into Blindness, which tells the first half of Sally’s story.

During Lent, we often reflect on our limits—from dust we are, and to dust we will return. We remember that we will never be able to do everything we want to do, even and especially when what we want to do is love our neighbor well. In this daily devotional, Disability rights activist Tatum Tricarico helps us turn the tables on Lent. Rather than a time of feeling condemned or guilty beyond help, Lent is when we can take a breath and finally say what we have been trying to hide all year: I am human. I can’t do it all. And still, I am beloved by God.

Jen Powley was diagnosed with multiple sclerosis at 15. By 35, she had lost the use of her arms and legs. Just Jen is a powerful memoir that tells the story of Powley’s life at the time of her diagnosis and the infinite, irrevocable ways it has changed since. Powley’s writing pulls no punches. She is lively, bold, and unapologetic, answering questions people are often afraid to ask about living with a progressive disease.

My friend Robby has a disability called ADHD. But that doesn’t matter to us. We play basketball, tell jokes, go canoeing, and help each other with our homework. I’m glad Robby is my friend!

From a social emotional learning expert: a book providing simple, science-based, practical advice including scripts, tips and strategies to help Neurodivergent adults who have ADHD, autism or anxiety find the belonging and support of lifelong friendships they seek. Friendship can be hard for...

In 2016, a United Nations report found the UK government culpable for ‘grave and systematic violations’ of disabled people’s rights. Since then, driven by the Tory government’s obsessive drive to slash public spending whilst scapegoating the most disadvantaged in society, the situation for disabled people in Britain has continued to deteriorate. Punitive welfare regimes, the removal of essential support and services and an ideological regime that seeks to deny disability has resulted in a situation described by the UN as a ‘human catastrophe’.

A year ago, Mr. Darcy suffered from an illness which robbed him of the use of his legs. However, he is determined to never become maudlin and behave as though his life is over and ruined just because part of it has become more difficult. Since he could not expect to recover any further, it was time to resume the ordinary course of his life.

Autism is often diagnosed during childhood but can also be diagnosed well into adulthood. If you feel you have been misunderstood your whole life, take heart, you are not alone.

David Aguilar was born missing part of one arm, a small detail that seemed to define his life and limit people’s ideas of who he was and who he could be. But in this funny and heartfelt memoir, David proves that he can throw out the rulebook and people’s expectations and maybe even make a difference in the world—and all with a sense of humor.

Jay reads Braille. Sam uses a wheelchair. Ben has Down syndrome. In this series, young listeners can learn more about how to be a good friend to friends with different capabilities and conditions.

An urgent and deeply affecting account of America's failure to provide meaningful support to its chronically ill and disabled citizens and our resulting reliance on the unpaid caregiving labor of spouses and intimate partners. When twenty-seven-year-old Laura Mauldin moved to New York for...

NEW YORK TIMES BESTSELLER | USA TODAY BESTSELLER | PUBLISHERS WEEKLY BESTSELLER | 2025 CHILDREN'S BOOK COUNCIL MIDDLE-GRADE FAVORITE After accidentally injuring his neighbor, Matt Sprouts thinks he has "the Curse,” a hometown myth that ruins middle schoolers’ lives. Matt decides to solve the...

Learn about children who are blind, their challenges and adaptations, and their similarities with others.

Learn about children who are blind, their challenges and adaptations, and their similarities with others.

Some people need to wear leg braces. What does that mean? Listeners learn how leg braces can help and what daily life is like for someone who wears them.

The moment Spencer meets Hope the summer before seventh grade, it's...something at first sight. He knows she's special, possibly even magical. The pair become fast friends, climbing trees and planning world travels. After years of being outshone by his older brother and teased because of his Tourette syndrome, Spencer finally feels like he belongs. But as Hope and Spencer get older and life gets messier, the clear label of "friend" gets messier, too.

McKenna Barney is trying to hide her worsening eyesight and has been isolating herself for the last year. But at the request of her little sister, she signs up for a commemorative mail run race in the Canadian wilderness - a race she doesn't know if she can even see to run. Winning would mean getting her disease - and her sister's - national media coverage, but it would also pit McKenna and her team of eight sled dogs against racers from across the globe for three days of shifting lake ice, sudden owl attacks, snow squalls, and bitterly cold nights.

From a very young age, Judy Heumann heard the word NO. When she wanted to attend public school, the principal said NO. When she wanted her teaching license, the New York Board of Education said NO. Judy and people with disabilities everywhere were tired of hearing “NO”. In the 1970s, an important disability rights law, Section 504 of The Rehabilitation Act of 1973, was waiting to be signed. Judy and other disability rights activists held a sit-in until Section 504 was signed into law, laying the foundation for the Americans with Disabilities Act.