Showing titles in People with Disabilities

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.

When twenty-nine-year-old Christine Schrader was diagnosed with stage four colorectal cancer, she refused to let fear or statistics define her. Instead, she opened her heart—and her journal—sharing the raw reality of treatment, the strength of family, and the stubborn joy she found in small, everyday moments. How Cancer Improved My Life is Christine’s story in her own words: candid, faith-filled, and often laced with the humor that carried her through more than sixty rounds of chemotherapy.

Every dyslexic person has their own story. This is my story; my story of discovery. My story of taking ownership and realising that my so-called disability is my greatest gift This is not a conventional audiobook about dyslexia. This is an audiobook about you! You truly conquering your dyslexia, and not being totally reliant on a school, your parents, or other people, but being reliant on yourself. Not letting dyslexia hold you back but push you to become the best version of yourself.

In Your Superpower, Tasha will describe how she overcame hurdles growing up to feeling confident in embracing who she is now. She will interview people from all walks of life to detail disabilities and differences of all kinds, such as blindness, alopecia, acne, mental health, and will show how you can use your difference to make a difference.

Trente-deux ans, c'est le nombre d'années qu'il m'a fallu pour mettre un nom sur ma différence. Comment ai-je pu "passer au travers des mailles du filet" durant tout ce temps ? Je vous révèle, au travers de ce récit parsemé d'anecdotes, comment j'ai grandi dans l'ignorance de mon syndrome. Plongez dans mon quotidien et découvrez chacune des étapes clés de mon évolution ainsi que les moyens mis en œuvre pour survivre dans ce monde parfois difficile à appréhender.

Brought to you by Penguin. Meet Lionel, Caroline’s older brother. Born in the 1950s, when little was known about autism, Lionel was considered a peculiarity. From the beginning, he was a silent child, oblivious to the people around him and intent only on playing with his toy trucks. By the...

MIND ESTRANGED tells the story of Bethany’s life, from her years as a promising university student through her gradual descent into schizophrenia, and unexpected, full recovery. While slowly losing her sanity, she traveled the world. She returned to the U.S. unable to work or study—and soon found herself homeless, delusional, and controlled by voices that talked to her and gave her orders in her mind. Bethany’s memoir enables the listener to enter into the mind of a person with schizophrenia, homeless and roaming the streets.

This memoir was written to honor my youngest brother’s influence over my life—the good, the bad, and the ugly, of living with a Down Syndrome sibling. It tells the story of the children of my family, despite our parents’ frailties, remaining committed to each other through life’s many changes and separations. Who I am today is directly related to who I needed to become.

An upcoming book to be published by Penguin Random House...

Just like fox, Heidi has lived on the outer. The ‘official record’ of her life has been her mental health record: primary diagnosis – schizoaffective; comorbidity – major depression, juvenile autism and not her own memories. This is the living, breathing version of Heidi’s mental health file that psych wards, doctors, mental health staff or rehab workers know little about or worse, use as evidence of diagnoses. This is Heidi’s account of what happened, shadowed by the story of a fox who knows he'll never belong.

In I'll Pray for You and Other Outrageous Things Said to Disabled People, Hannah Setzer volunteers to go first and say the things that we all think, but rarely say. Hannah has lived her whole life as a disabled woman and is here to share her story, though don't think for a second that this is inspiration porn. In fact, Hannah's disability is the least interesting thing about her!

Twenty-three-year-old Ardra Shephard is sleeping with the wrong guy, living in a crappy apartment, and spending money she doesn't have on designer shoes, boozy brunches, and weekends in NYC. Making mistakes while you figure stuff out is what your twenties are all about. Then a doctor tells Ardra she has MS, and those two letters split her life into a Before and After.

Outlaw Patients is a raw, darkly funny, and fiercely honest memoir about trying to survive in a system that wasn’t built to help. Medical marijuana patient and longtime activist Russell Barth takes listeners inside the chaotic, painful, often absurd world of Canadian cannabis policy — and the strange place where medicine, bureaucracy, and rebellion overlap.

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.

After 30 years of a healthy, rewarding, and exciting life, I wake up in a hospital bed unable to move. The neurosurgeon leans down and breaks the news: You won't regain any function in your body and you will never walk again. My medical insurance sends me home, discontinues my care, and tells me to "adapt to my new life". Little Big Steps is the story of the pivotal moments, interactions, and breakthroughs following the injury that turned my life upside down.

This program is read by the author. Confessional and often hilarious, in Normal Sucks a neuro-diverse writer, advocate, and father meditates on his life, offering the radical message that we should stop trying to fix people and start empowering them to succeed. Jonathan Mooney blends anecdote...

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...

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.

Imagine if you were to lose your sight? Would it feel like the end of everything worthwhile? There is a way forward. Once you realise that blindness is a word and not a sentence, life takes on a new perspective. There are ways to thrive with vision loss. This book reveals how to turn such a life-challenge into a lifestyle you can fully manage and enjoy.

A profoundly beautiful memoir about disability, difference, and living as a vulnerable body. Jan Grue had just become a father when he inherited a stack of his childhood medical records. Following a diagnosis of spinal muscular atrophy at the age of three, the raft of doctors' notes, clinical descriptions and case histories defined his body as defective and his future as bleak and limited. They conjured a childhood nothing like the one he remembered, that failed to anticipate the life he lived now. "I Live a Life Like Yours" is Grue's beautiful, groundbreaking search for a literary language that could better tell his story.