Showing titles in People with Disabilities

In 1997, Daniel Trush, a bright, active, outgoing twelve-year-old, collapsed on the basketball court and fell into a deep coma. Rushed to the hospital, he was found to have five previously undetected aneurysms in his brain. One had burst, causing a massive cerebral hemorrhage. While Daniel remained comatose, the uncontrolled pressure inside his skull caused him to suffer multiple strokes.

Finalist for the Pulitzer Prize in Memoir or Autobiography A New York Times Notable Book of 2022 * Vulture’s #1 Memoir of 2022 * A Washington Post, Los Angeles Times, USA TODAY, Time, BuzzFeed, Publishers Weekly, Booklist, and New York Public Library Best Book of the Year * One of Oprah...

A lively memoir of growing up with blind African American parents in a segregated cult preaching the imminent end of the world—for fans of James McBride’s The Good Lord Bird. It’s 1970, and Jerry Walker is six years old. His consciousness revolves around being a member of a church whose...

Penny Fisher is on vacation with her family when she becomes ill and disoriented. An urgent care facility reads her temperature at 104.5 and sends her by stretcher to the emergency room. There, doctors find nothing wrong, and they send her home. Twenty-four hours later, Penny is on life support and her husband is told to say his goodbyes.

Henry Markram is the Elon Musk of neuroscience, the man behind the billion-dollar Blue Brain Project to build a supercomputer model of the brain. He has set the goal of decoding all disturbances of the mind within a generation. This quest is personal for him. The driving force behind his grand ambition has been his son Kai, who has autism. Raising Kai made Henry Markram question all that he thought he knew about neuroscience, and then inspired his groundbreaking research that would upend the conventional wisdom about autism, expressed in his now-famous theory of Intense World Syndrome.

We were walking this journey together, yet alone. Two siblings from a close-knit, boisterous family of six. There is nothing like the camaraderie of family to give you the determination to persevere in spite of any obstacle. We were overwhelmed by the disease of multiple sclerosis as well as other autoimmune diseases. Our outward appearance of healthiness was deceiving. Unbeknownst to us, the disease of multiple sclerosis would eventually consume mobility, sight, memory, fine motor skills, speech, and so much more.

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...

Have you ever wondered how a blind person pours a cup of coffee? Or how they and their guide dog know when it's safe to cross a busy road? When Lois Strachan lost her sight at the age of 21 years, she had to learn the answers to these and countless other questions of how to live as a blind person in a sighted world. In this delightfully quirky and entertaining book, Lois shares some of the secrets she discovered about how to live an “ordinary” life in an extraordinary way despite her disability.

The author describes in detail all the insanity, disturbing behaviors, oppressive symptoms, and various feeling associated with the mental battles within her own mind. The author suffers from clinical depression, bipolar disorder, schizophrenia, schizoaffective disorder, and borderline personality disorder. She struggles with suicidal thoughts and attempts, self-mutilating behaviors, mania, paranoia, anxiety, and psychosis with intense hallucinations of all five of her senses, and multiple delusions, including the belief that she is the "second-coming of Christ".

The stories in this book are about women who are married to, or were once partnered with, men on the mild end of the autism spectrum, formerly known as Asperger’s syndrome. These women are not autistic, so their relationships are considered neurodiverse (meaning there’s a neurotypical person in a relationship with a neurodivergent person). The focus within the stories is Cassandra Syndrome. A very life-altering phenomenon that often occurs—and usually remains unaddressed—within these relationships.

Inclusion isn’t always about grand gestures. Sometimes, it can begin in the smallest of moments. Inclusion Moments is a collection of short stories and reflections drawn from the lived and professional experience of the author, Poggy Murray Whitham, from the world of engineering and beyond, seen through their perspective as a Black, Queer, Disabled, and Autistic person.

Ellen Keane spent most of her teens uncomfortable with her limb difference and battling to hide her insecurities. It was only when she embraced her difference that she found her superpower. She started to believe in her unique abilities and gradually find the success that she had never dreamed possible. Perfectly Imperfect is for anyone struggling to accept who they are. With anecdotes from her own life, practical advice and good-natured humour, Keane challenges you to let go of waiting until everything is perfect and instead embrace your imperfections and accept who you are, flaws and all.

For years, they came in on weekends to plan and practice—nearly sixty surgeons, nurses, and anesthesiologists, preparing to harmonize in a vast medical symphony. For the team at Mayo Clinic, it was their most complex surgery to date: a face transplant. At the heart of this event was Andy Sandness. He grappled with feelings of isolation and shame after a disfiguring suicide attempt but was determined to reclaim his future, to be seen as ordinary, and to belong again.

While preparing to deploy with the US Army, Marcus suffered a severe spinal injury that left him paralyzed. After dying on the operating table twice, the surgeons saved his life, but told him he'd never walk again. Having no other option, Marcus started doing some brutally honest soul-searching, looking for the lesson to be learned from his injury. Once he started seeing his adversity as a gift instead of a curse, something miraculous began to happen....

Author Eiren Caffall is the inheritor of a family legacy of two hundred years of genetic kidney disease and the mother of a child who may inherit that legacy. A literary memoir on loss, chronic illness, and generational healing, Caffall’s The Mourner’s Bestiary is also a meditation on grief and survival told through the stories of animals in two collapsing marine ecosystems—the Gulf of Maine and the Long Island Sound—and the lives of a family facing a life-threatening illness on their shores.

"Ich bin einer derer, die die Jahreskarte gezogen haben. Wenn ich abrutsche oder hochfliege, dann für eine lange Zeit. Dann bin ich nicht mehr zu halten, ob im Flug oder im Fall." Die fesselnde Chronik einer manisch-depressiven Erkrankung: ein autobiografisch radikales Werk von höchster literarischer Kraft.

Born in Tuscumbia, Alabama in 1880, Helen Keller lived the first two years of her life as any normal seeing and hearing child might. Then, one dreary February, Helen was stricken with a mysterious illness that left her blind and deaf. It wasn’t until the age of six, when Miss...

Cory Smit never had a chance to grow up as a normal kid. Between the extreme views pushed on him in church to being bullied at a series of schools, it took years to understand the worst of his trouble at home. After surviving physical and psychological trauma at the hands of his adoptive parents, Cory entered custody of the State of Arizona through a series of misunderstandings and misguided interventions.

Sarah Merriman is just like any other urbane young woman in her twenties... She has a job in a Central London hotel, a boyfriend, commutes to work on the Tube, eats out, goes to films and theatre... This is all the more remarkable (though not to her) because Sarah was born with Down's Syndrome. Her parents having no prior inkling, it came as a huge shock to them that they now had a daughter with a disability. In 1999 her father Andy wrote a frank and moving book, A Minor Adjustment, about the challenge of her early years. Now he continues with this inspirational story.

Disability activist and social media influencer Melissa Blake offers a frank, illuminating memoir and a call to action for disabled people and allies. In the summer of 2019, journalist Melissa Blake penned an op-ed for CNN Opinion. A conservative pundit caught wind of it, mentioning Blake’s...