Social Disabilities

An unflinching and luminous memoir that explores a father’s philosophical transformation when he must reconsider the questions what makes us human? and whose life is worth living? Before becoming a father, Chris Gabbard was a fast-track academic finishing his doctoral dissertation at Stanford. A disciple of Enlightenment thinkers, he was a devotee of reason, believed in the reliability of science, and lived by the dictum that an unexamined life is not worth living. That is, until his son August was born.

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!

Si no es cada cuatro años que se celebran los paralímpicos, si no se acerca el Día Internacional de las pcd, cuando las marcas realizan acciones; si no es que el gobierno da beneficios fiscales para impulsar la inserción laboral de este grupo, el resto del tiempo las personas con discapacidad viven entre las sombras.

Three months into her pregnancy with her first child, Hilary Yancey received a phone call that changed everything. As she learned the diagnosis - cleft lip and palate, a missing right eye, possible breathing complications - Hilary began to pray in earnest. Even in the midst of these findings, she prayed that God would heal her son. God could do a miracle unlike anything she had seen. Only when Hilary held her baby, Jack, in her arms for the first time did she realize God had given her something drastically different than what she had demanded.

After her elderly owner passes away, Star—a deaf Australian shepherd—is brought to a local shelter. Star feels scared and alone—until she meets 12-year-old Julian. After getting in trouble at school yet again, Julian volunteers at the shelter and realizes he can communicate with Star in a way that no one else can. Their bond continues to grow, and Julian and Star become inseparable. Then the unthinkable happens: Funding for the shelter dries up. The only way to save Star is to adopt her, but he has to prove that he can stay out of trouble and train a dog like Star.

With Mental Health, Inc., award-winning investigative journalist Art Levine delivers a Shock Doctrine-style exposé of the failures of our out-of-control, profits-driven mental health system, with a special emphasis on the failures of the pharmaceuticals industry, including the treatment of children with antipsychotics and disastrous PTSD protocols for veterans.

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.

This biography is an excellent and accessible introduction for youngsters to learn about one of the world's most influential luminaries. Helen Keller's poignant narrative is beautifully captured in this unforgettable portrait of a woman whose vision for innovation and progress changed America and the world forever.

Robert Hoge was born with a giant tumour on his forehead, severely distorted facial features and legs that were twisted and useless. His mother refused to look at her son, let alone bring him home. But home he went, to a life that, against the odds, was filled with joy, optimism and boyhood naughtiness. Home for the Hoges was a bayside suburb of Brisbane. Robert's parents, Mary and Vince, knew that his life would be difficult, but they were determined to give him a typical Australian childhood.

Disability and Political Representation explores how disabled people experience the various stages and aspects of the representation process, drawing upon extensive empirical research and a variety of qualitative and quantitative data. It discusses why increasing the number of disabled politicians matters, not only as a matter of justice and equality but also to better represent the issues and interests of importance to disabled people.

Deaf and homeless his entire adult life, Butch discovers a wallet in a dumpster. What he does next will lead to a chance encounter with a visitor from Texas. This is a true story of survival by eating out of dumpsters and trying to keep warm with restroom hand dryers. More, it is a story of an unlikely friendship that has lasted over twenty-five years. Share through Butch’s own letters his sustaining faith and hope to be a somebody. You will cry. You will laugh. You will learn.

In the second edition of About Canada: Disability Rights, Deborah Stienstra explores the historical and current experiences of people with disabilities in Canada, as well as the policy and advocacy responses to these experiences. Stienstra demonstrates that disability rights enable people with disabilities to make decisions about their lives and future, claim rights on their own behalf, and participate actively in all areas of Canadian society.

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.

Invisible Visibility discusses the key barriers that marginalize disabled artists from taking center stage and looks at examples of good practice through three key case studies. This audiobook puts forward an agenda for change, inclusion, and, ultimately, visibility within the sector and beyond for disabled dancers from culturally diverse backgrounds.

My name is Harper Drew. I'm using my new journal to take note of all the totally ridiculous things that seem to go on around me with my family and friends. I seem to be the only one who sees all of this stuff for what it is. Completely beyond normal. Recently I've been logging Drew Dial Ratings for all the mayhem. On a scale of zero to 10, how likely is someone to say or do something that would be less sensible than (for example)...a demented camel?

My friend Darius has a disability called dyslexia. But that doesn’t matter to us. We make our own comics, help each other with our homework, and volunteer at a nearby animal shelter. I’m glad Marius is my friend!

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

Some people use wheelchairs to get to and from places. What does that mean? Listeners learn why someone would use a wheelchair and what daily life is like for someone who can't walk.

This joyful audiobook with an empowering refrain, from disability rights activists Jessica Slice and Caroline Cupp, demystifies and respects how disabled people and their families use adaptive, imaginative, and considerate play so everyone can join in the fun.

Challenging the view that autism is something that needs to be ‘cured', Virginia Bovell testifies to the extraordinary care Danny has received for over 30 years and the everyday kindness and decency of the people – ‘the band of angels' – that surround him. She asks us to consider what makes a thriving individual versus an inadequate one; what it means to be ill versus what it means to not to conform; what roles society values and rewards; and how humans might flourish outside of failing political and economic systems.