Disability Science

Disability is often described as a tragedy, a crisis, or an aberration, though 1 in 5 people worldwide have a disability. Why is this common human experience rendered exceptional? In All Our Families, disability studies scholar Jennifer Natalya Fink argues that this originates in our families. When we cut a disabled member out of the family story, disability remains a trauma as opposed to a shared and ordinary experience. This makes disability and its diagnosis traumatic and exceptional.

There is a middle world between life and death, and Tess must navigate it to save her brother in this heart-wrenching story infused with the fractured and fantastical realms of Finnish mysticism. Axel and Tess are bewildered when a stranger shows up in their backyard accompanied by a giant brown bear, but before they can investigate the bizarre encounter, something more harrowing happens: their father is killed in a freak car accident.

When hell on Earth comes in the form of a virus-born zombie apocalypse, the virus that is at the center of the mayhem meets its match in the brain of an unlikely foe: an autistic girl named Zoe....

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.

Texas governor and rising star in the Republican Party - one of the first prominent politicians to govern from a wheelchair since Franklin D. Roosevelt - Governor Greg Abbott pens his deeply personal and inspiring life story and proposes a plan to restore America to greatness in what Newt Gingrich calls a "bold and compelling" read. Texas Governor Greg Abbott lost his ability to walk when a huge oak tree crashed down on his back, fracturing vertebrae into his spinal cord, leaving him forever paralyzed.

One million cloned soldiers. A nation imprisoned. A group of neurodiverse rebels fighting back. Britain as we know it lies destroyed. In the aftermath of the most daring military coup in history, the surviving population is crammed inside giant citadels, watched over by an army of cloned soldiers. The hope of a nation lies in a tiny number of freedom fighters hidden in the abandoned countryside, most of whom are teenagers who escaped the attack on their special school.

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.

He Called Me Tin is a story of triumph and perseverance. From childhood distress to an attempt at suicide to being scarred by religion to being diagnosed with multiple sclerosis to the strife of racism and discrimination as a government employee to being assaulted and nearly kidnapped abroad, she has overcome in peace....

Twelve-year-old Amberly doesn’t quite fit in with all the other fairies in Whimsical Land. One of her wings is undersized and paralyzed, and instead of flying she has to run and leap through the air with the help of a stick. It’s awkward, it’s no fun, and she sometimes gets bullied for it, too. Worse than that, her mother worries about her disability and won’t let her take sword-fighting lessons with her sorcerer uncle.

Here, you’ll find answers to your questions regarding what it means to be diagnosed with autism, what the warning signs are, common co-occurring diagnoses, and what the intervention options are. This audiobook will also explain how to respond to an autism diagnosis, the parent’s role, and how to support your child. In addition, we will address parental concerns and frequently asked questions. It will give you all the tools you need to deal with everyday concerns, such as social skills, traveling, school, and so much more!

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.

Things That Are continues the story of Bobby Phillips - the boy who woke up one day to find himself invisible - and his friend and confidante, a blind girl named Alicia. Bobby is returning from college visits in New York, and Alicia has decided to finally confront him about her feelings. But a mysterious character with an affliction similar to Bobby's and some surprise visits from the FBI threaten to destroy everything.

Developing a cybernetic model of subjectivity and personhood that honors disability experiences to reconceptualize the category of the human.

With the deadly phantom sgàilean defeated, Jaime and Agatha prepare to help their clan reclaim their compound from the treacherous Raasay people. But Sigrid, sent at the behest of Queen Beatrice, arrives with a warning: the kings of Norveg and Ingland have joined forces and plan to march north to annihilate the people of Scotia. The clan quickly turns to the Badhbh and his powerful blood magic. But instead of aiding them, the mage kidnaps Agatha, seemingly as an offering to the kings.

What does it mean to "know" something? While the answer to this question has been traditionally defined by the content of an individual's mind, artificial intelligence technology, or AI, has the potential to completely redefine the notion. In no context are discussions of "what it means to know" more relevant than in those surrounding individuals with cognitive disabilities - unique individuals who struggle with knowing daily.

We think of perception as a passive, mechanical process, as if our eyes are cameras and our ears microphones. But as neurobiologist Susan R. Barry argues, perception is a deeply personal act. Our environments, our relationships, and our actions shape and reshape our senses throughout our lives. This idea is no more apparent than in the cases of people who gain senses as adults. Barry tells the stories of Liam McCoy, practically blind from birth, and Zohra Damji, born deaf, in the decade following surgeries that restored their senses.

On July 4th, 2013, Connor Sparrowhawk, also known as Laughing Boy or LB, was found dead in a specialist NHS unit. Connor, who had autism and epilepsy, had a seizure while in the bath, and no member of staff was on hand to stop him from drowning. An entirely preventable death. Sara Ryan presents a frank, sometimes funny and touching account of her son's early life and preventable death and the unfolding #JusticeforLB campaign.

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.

For over twenty years, Dara Baldwin has often been the only person of color in the room when significant disability policy decisions are made. Disenfranchisement of people of color and multi-marginalized communities within the disability rights community is not new and has left many inside the community feeling frustrated and unheard. In Demanding Solidarity, Baldwin candidly shares her journey to becoming a disability activist and policymaker in DC while critiquing the disability rights community.

Sabine Heinlein spent almost a year reporting at "The Farm", a program for mental patients at the notorious Creedmoor Psychiatric Center in Queens. Originally designed to teach its "members" confidence and skills by caring for animals and plants, the Farm had long become a dysfunctional hoarder's den. The patients sat idly on chairs in a grimy dayroom filled with the therapist's "collectibles" and garbage.