Disability Science

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.

The success of food allergy activism in highlighting the dangers of foodborne allergens shows how illness communities can effectively advocate for the needs of their members. In Food Allergy Advocacy, Danya Glabau follows parents and activists as they fight for allergen-free environments, accurate labeling, the fair application of disability law, and access to life-saving medications for food-allergic children in the United States.

Seventeen-year-old Merry has mucked up another chance to get into the University of Magecraft, so she doesn’t have time to deal with shape-changing creatures bent on stealing memories from the people of Woodshire. That’s her father’s job. But when an outlaw mage mistakes her for a damsel in distress on a drenched train platform, she’s dragged into a fight with the monsters and a sheriff mad enough to use them. She’d never admit it out loud, but the mage is actually kind of fun to work with—when she doesn’t want to run him over with her chair.

Da Rosa bliver født i en lille provinsby i slutningen af 1800-tallet, er hendes muligheder i livet allerede yderst begrænsede. Hun er pige i et mandsdomineret samfund, men ydermere har hun et medfødt handicap - hun er med datidens sprogbrug vanfør. Vi følger først Rosas tilværelse som barn i provinsen, hvor hun møder stor fordømmelse fra omgivelserne, fordi hun er anderledes. Siden hører vi om hendes ophold på et vanførehjem i København. Romanen beretter både om de dårlige vilkår, mennesker med handicap havde i slutningen af det 19.

Public Hostage, Public Ransom starts with the autobiographical story of William Bronston, the activist physician whose early professional California training steels him with a deep moral, professional, and cultural bond to the huge 6,000-person disabled population he encounters incarcerated in Willowbrook State School in Staten Island, NY, on whose behalf he daily battles to humanize and ultimately catalyze a federal class action lawsuit against the state to close the death-making institution.

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....

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!

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.

Since being adopted by the king and queen of Starrycrest two years ago, Kara has lived a magical life, complete with doting parents and staff as well as a starring role in the Starrycrest Starlets' production of The Nutcracker. The princess is on top of the world, until big changes threaten her place in the Denison family as well as in the kingdom. Kara's magical life quickly turns into a nightmare when she is forced to face her deepest insecurities and prepare for the biggest night of her life with a dance partner whom she does not even like.

This book is user-friendly. Each chapter will be dedicated to one month. Within each chapter, there will be a subsection for each week. Subsequently, a passage for each day will give the listener a slice of what it means to live with a disability. By taking this cultural journey, the listener will be able to interact with the disabled community and other minority groups authentically.

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.

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.

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.

Natalie O'Rourke was an ordinary little girl from Birmingham in all respects save one: she was lonely. When she discovered how much she loved horses, she decided she wanted to grow up and run a riding stables. She wanted her stables to cater for children and adults with disabilities, additional needs and anyone who needed a friend—people who you might not expect to find riding, but who she knew could find happiness through horses, because she had.

Meg Zucker was born with one finger on each hand, shortened forearms, and one toe on each misshapen foot, caused by a genetic condition called ectrodactyly. She would eventually pass this condition on to her two sons, and, along with her husband, raise them and their adopted daughter, who has her own invisible differences. Born of the family’s hard-won experiences, this book offers invaluable advice on raising confident, empathetic, and resilient children who succeed, not despite but because of their differences.

For more than 40 years, professionals in the field of disability studies have engaged in debates over the use of aversive interventions (such as electric shock) like the ones used at the Judge Rotenberg Center. This book is a historical case study of the Judge Rotenberg Center, named after the judge who ruled in favor of keeping its doors open to use aversive interventions.

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?