Social Disabilities

Despite the progress of decades-old disability rights policy, including the landmark Americans with Disabilities Act, threats continue to undermine the well-being of this population. The U.S. is, thus, a policy innovator and laggard in this regard. In Politics of Empowerment, David Pettinicchio offers a historically grounded analysis of the singular case of U.S. disability policy, countering long-held views of progress that privilege public demand as its primary driver.

This book explores gender, disability, and literature in the Global South, concentrating on Nepal in particular. Religious and cultural values disable women’s autonomy in general, and create even greater disadvantages for women who are physically disabled. This study examines two Nepali women writers, Bishnu Kumari Waiwa and Jhamak Ghimire, who challenge stigmas of the disabled body by deconstructing the “ideology of ability” through their autobiographical narratives.

In 2018, Joe Hammond, wrote a piece for the Guardian about the 33 birthday cards he was writing for his two sons. It was shared by thousands. In A Short History of Falling he tells the story behind that piece, about the experience of living with - and dying of - motor neurone disease (ALS). A Short History of Falling is not a lament. It is a deeply imaginative meditation on what it feels like to confront the fact that your family will persist through time without you.

As a boy, severely disabled after contracting polio as a baby in working class Liverpool, Bert Massie found himself wondering why disabled people were expected to adapt to the world around them, and not the other way round. In his teens, he began to campaign for rights for disabled people, and having battled his way through prejudice and the education system to become a Bachelor of Arts and a qualified social worker, he became a prominent figure in the fight for fair treatment for disabled people leading to the ground breaking Disability Discrimination Act.

Ben Mattlin lives a normal, independent life. Why is that interesting? Because Mattlin was born with spinal muscular atrophy, a congenital weakness from which he was expected to die in childhood. Not only did Mattlin live through childhood, he became one of the first students in a wheelchair to attend Harvard, from which he graduated and became a professional writer. His advantage?

The first significant book on the history and impact of the ADA - the "eyes on the prize" moment for disability rights. The Americans with Disabilities Act (ADA) is the widest-ranging and most comprehensive piece of civil rights legislation ever passed in the United States, and it has become the model for disability-based laws around the world. Yet the surprising story behind how the bill came to be is little known.

From the Periphery consists of more than 30 first-person narratives of everyday people who describe what it's like to be treated differently by society because of their disabilities. The stories are raw and painful, but also surprisingly funny and deeply inspiring. The oral histories describe anger, independence, bigotry, solidarity, and love - in the family, at school, and at the workplace. From the Periphery will become a classic collection that increases understanding of the lived experiences of people with disabilities.

In just four months receive your SSDI benefits! This concise guide is a book written to show you how to protect your money and investments if you become ill or have an accident and have to apply for disability. It is explained in a simple version of how to apply and receive in four months.

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.

When Emma Sasha Silver loses her eyesight in a nightmare accident, she must relearn everything from walking across the street to recognizing her own sisters to imagining colors. One of seven children, Emma used to be the invisible kid, but now it seems everyone is watching her. And just as she's about to start high school and try to recover her friendships and former life, one of her classmates is found dead in an apparent suicide. Fifteen and blind, Emma has to untangle what happened and why - in order to see for herself what makes life worth living.

In his debut novel, YouTube personality and author of We Should Hang Out Sometime Josh Sundquist explores the nature of love, trust, and romantic attraction. On his first day at a new school, blind 16-year-old Will Porter accidentally groped a girl on the stairs, sat on another student in the cafeteria, and somehow drove a classmate to tears. High school can only go up from here, right?

Colin Fischer cannot stand to be touched. He does not like the color blue. He needs index cards to recognize facial expressions. But when a gun is found in the school cafeteria, interrupting a female classmate's birthday celebration, Colin is the only for the investigation. It's up to him to prove that Wayne Connelly, the school bully and Colin's frequent tormenter, didn't bring the gun to school. After all, Wayne didn't have didn't have frosting on his hands....

High school senior Jesse Alderman, or Sway as he's known, could sell hell to a bishop. He also specializes in getting things people want—term papers, a date with the prom queen, fake IDs. It's all business with Jesse. He has few close friends and he never lets emotions get in the way.

Jamey Barlowe has been crippled since childhood, the result of being born on the Moon. He lives his life in a wheelchair, only truly free when he is in the water. But then Jamey’s father sends him, along with five other kids, back to the Moon to escape a political coup d’etat that has occurred overnight in the United States. Moreover, one of the other five refugees is more than she appears. Their destination is the mining colony, Apollo. Jamey will have to learn a whole new way to live, one that entails walking for the first time in his life.

In a relatable, positive, and compassionate voice, disability advocate and social media content creator Beth Leipholtz introduces twenty-six real kids with autism, hearing differences, epilepsy, Down syndrome, and more than a dozen other diagnoses. Their stories remind us that people with disabilities are all around us, and all children deserve to be seen, heard, valued, understood, and loved.

Two million people in the UK live with sight loss, and many more worldwide. Yet the general population knows very little about the day-to-day life of the blind, who must move through a world not designed with them in mind, from city planning and technology, to pop culture and education. What’s more, blind people often fall off the pages of our history books, despite being some of the most prolific figures in their fields.

Creating a force called lift, counteracting the outside energy that would otherwise pull her down, that is the way Anna Gouker spends her days. Anna understands the importance of an elevated focus. This enables her to reach higher than the outside world may say is within her grasp. Anna has a degenerative muscle weakness that persists throughout her body, requiring her to depend greatly on technology - like the ventilator that helps her breathe while she sleeps and the motorized wheelchair that moves her through the world.

Kate’s life in Baton Rouge, full of friends and family, gymnastics and Girl Scouts, is just plain great. But then, at the age of twelve, she suddenly develops a mysterious shoulder pain that won’t go away . . . and that will change her life forever. It turns out that Kate has one of the rarest genetic disorders in the world, Fibrodysplasia Ossificans Progressiva. FOP causes bone to form in places in the body where it shouldn’t, and there’s no cure yet.

While finishing off her degree in Gerontology at Umass Boston, Yvonne Decelis started writing about her life in the hope of showing others with similar conditions that they are not alone in the trials they face. Yvonne goes over her upbringing and life prior to, during, and after diagnosis covering things like medications, “healthful living”, work, SSDI disability benefits, friendships, and relationships, etc. This was also written for people seeking information on how to interact with others who have "invisible illnesses" like MS, Fibro, Post-traumatic Stress injury, etc.

Told through an experimental mix of intimate anecdotes and interactive visuals, this book immerses listeners in Emmy Award-winning documentary filmmaker James Robinson's point of view, allowing them to see the world through his disabling eye conditions.