Disability Memoir

Blindness. A tough topic to discuss? Not anymore. In this groundbreaking book, listeners will see blindness in a whole new light. In fact, the compelling and entertaining stories will not only change perceptions of blindness, they’ll make listeners forget the people featured are actually blind.

For many years, Jeffrey Demitrack searched for a meaningful and fulfilling relationship and, most of all, hoped that one day he would find a significant other who understood and unconditionally accepted his struggles with epilepsy. People have their insecurities, and relationships already are hard without throwing seizures into the mix, so his search has been a challenging one.

Amit Patel is working as a trauma doctor when a rare condition causes him to lose his sight within 36 hours. Totally dependent on others and terrified of stepping outside with a white cane after he's assaulted, he hits rock bottom. He refuses to leave home on his own for three months. With the support of his wife, Seema, he slowly adapts to his new situation, but how could life ever be the way it was? Then his guide dog, Kika, comes along....

An unflinching and luminous memoir that explores a father’s philosophical transformation when he must reconsider the questions what makes us human? and whose life is worth living? Before becoming a father, Chris Gabbard was a fast-track academic finishing his doctoral dissertation at Stanford. A disciple of Enlightenment thinkers, he was a devotee of reason, believed in the reliability of science, and lived by the dictum that an unexamined life is not worth living. That is, until his son August was born.

Daddy Won’t Let Mom Drive the Car: True Tales of Parenting in the Dark is a book of short vignettes - most of them lighthearted, a few more serious - about my life as the blind mother of a sighted daughter. Welcome to my journey! My blindness has changed a few practical logistics. But in the end, kids are kids and moms are moms, and the dents and delights of parenthood are universal.

Rachel Kolb was born profoundly deaf the same year that the Americans with Disabilities Act (ADA) was passed, and she grew up as part of the first generation of deaf people with legal rights to accessibility services. Still, from a young age, she contorted herself to expectations set by a world that prioritizes hearing people. Now in Articulate, Kolb blends personal narrative with cultural commentary to explore the different layers of deafness, language, and voice.

As director of legendary Pommery Champagnes, Philippe Pozzo di Borgo was not generally someone in the habit of asking for help. Then, in 1993, an accident left him a quadriplegic. Passing his days hidden in his Paris townhouse, Philippe found himself the modern equivalent of an “untouchable.” The only person who seemed not to be bothered by Philippe’s condition was someone who had been marginalized his entire life - Abdel, the unemployed, uninhibited immigrant from the outskirts of society who would become Philippe’s caretaker.

Backbone is a life-fulfilling message about managing chronic pain and living a life of purpose. For two decades, Karen Duffy, New York Times bestselling author, former MTV VJ, Revlon model, and actress, has managed to live an enriching life despite living in a state of constant pain. In this powerful, inspirational, funny, and important manual for surviving pain, Duffy draws on her experience as a patient advocate, trained recreational therapist, and hospice chaplain to illuminate gratifying methods people can use to cope with chronic pain.

This is a philosophical and observational book based on the challenges and the triumphs of Paddy Slattery's life which include a severe spinal cord injury leaving him paralyzed, two near-death experiences, and his debut film hitting the cinema and Netflix just as Covid was beginning to make headlines.

Dr. Paul Boskind, a successful psychologist and LGBTQ+ advocate, thought he had everything under control. Diagnosed with a blinding retinal disorder at twenty-one, he defied the odds, building a fulfilling life. But years earlier than expected, his vision began to fade. The Blind Man Game is Paul’s poignant journey of self-discovery as he navigates the emotional turmoil of losing his sight and sense of self. With his future uncertain, Paul must draw on his expertise and inner strength to confront grief, fear, and a world no longer designed for him.

DEMENTIA and OUR LOVE, Caregiving as spiritual practice, is the story of Gary and Heather's love that sustained them through an unusual and courageous life across continents, including tending Gary and his onset of dementia at 73 years. The story helped them remember their love and use this energy to move through the hard times. We will always remember us this way, a song by Lady Gaga, was pivotal in keeping Heathers focus.

Wayne Magee is on a mission to empower those who have been repeatedly told, “You can’t!” He has spent his life overcoming obstacles and negative labels intended to convince him that he could not lead a purposeful, fulfilled life. At birth, he was diagnosed with cleidocranial dysplasia, which is a rare genetic skeletal disorder that affects one in one million people. Countless medical professionals stated that he would not live beyond two years old. Wayne’s story demonstrates that for every tough blow, we have an innate ability to overcome societal and medical challenges.

Sandra Allen did not know their uncle Bob very well. As a child, Sandy had been told Bob was “crazy”, that he had spent time in mental hospitals while growing up in Berkeley in the '60s and '70s. But Bob had lived a hermetic life in a remote part of California for longer than Sandy had been alive, and what little Sandy knew of him came from rare family reunions or odd, infrequent phone calls. Then in 2009, Bob mailed Sandy his autobiography.

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".

In this unique and exhilarating autobiography, Allan Jones - Canada’s first blind diplomat - vividly describes how an untreatable eye disease slowly decimated his visual world, most challengingly during his postings in Tokyo and New Delhi, and how he discovered and took to heart the revelatory Indian philosophy that changed his life.

The Magic Circle tells the story of what happens when Charmaine Chan's sister Elaine is diagnosed with a rare and aggressive cancer. As the illness progresses, family members living on different continents gather together during Elaine's last days. Striving to distract Elaine from the worst effects of the cancer, Charmaine takes to the pen: conjuring up the vanished world of their childhood in Singapore, and discovering a way to keep her promise to Elaine's six-year-old daughter.

There are 1.3 billion people around the world who identify as having a disability. When you include friends and family, the disability market touches 53 percent of all consumers. It is the world’s largest emerging market. Unleash Different reveals how companies like Google, PepsiCo, and Nordstrom are attracting people with disabilities as customers and as employees. Replacing “nice to do” with “return on investment” allows market forces to take over and the world’s leading brands to do what they do best: serve a market segment - in this case, the disability market.

Everyone always ask me what it is like being autistic. The reality is, being autistic is unique to each person. In this audiobook, I explain an aspect of my autism called "escaping into imagination" and how I use it to create a make-believe world to accelerate how amazing my autism is. It has often been said that people with autism struggle with pretend-play. I feel this is a misunderstanding. Just because we do not pretend play like other kids does not mean we do not have imaginations or use them to pretend in our own world.

This memoir combines the drastic losses which occur due to severe episodic memory deficits with the greater agency currently afforded to all of us as made capable via ingenuity and technology. In this book memory loss is considered within the present-day environment of novel solutions heretofore unimaginable. All of us may never need to worry about recalling key life events ever again.

Carly-Jay Metcalfe was born with cystic fibrosis, survived a double-lung transplant at the age of 21 and faced a rare cancer at the age of 30. What she has endured should have killed her, but her humour, courage and optimism became her best survival skills. From her hospitalised childhood to her many friendships, loves and losses, Metcalfe shares the fickle nature of life with candour and warmth. She writes with compelling insight about organ donation, opioid addiction and survivor's guilt, while still managing to find joy amongst the wreckage.