Showing titles in People with Disabilities

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!

After a shocking diagnosis for a rare pituitary disease, and with her eighteen-year marriage in shambles, Risa's life has fallen far from picture-perfect. Recovering from brain surgery and desperate to get back to her former self, she signs up for the bike tour of a lifetime-six weeks from Canada to Mexico on the Pacific Coast Highway. The old Risa could have done the ride in her sleep, but for the new Risa, trapped in a body that no longer feels like her own and stuck in the company of her brain tumor, Bubba, the ride becomes a challenge unlike anything she's ever faced.

James Partridge was 18 years old in 1977 when his face and body were severely burned in a car accident. Refusing to succumb to society's expectations, James chose not to hide in the shadows, but to succeed despite his distinctive face and live a happy and hugely successful life, both personally and professionally. Face It tells the story of James' recovery and the work he has done ever since to support others with physical differences to cope with the isolation and discrimination they so often face.

“I never wanted to be hearing. I said this out loud in my TED talk, and the audience went bug-eyed, struggling to process this heresy. How could anyone not want to be hearing? I wasn’t anti-hearing. I just felt my life would be simpler if everyone else were deaf.” So begins the compelling story of acclaimed TED speaker Rebecca Knill as she guides us through a life shaped by hearing loss. Throughout, Knill offers eye-opening insights into disability and celebrates the power of technology to level the playing field.

This book is about one big rollercoaster. It's about a girl who has CP (cerebral palsy) and the challenges she has faced throughout her life. A girl who is lucky to be blessed with people who stood beside her all the way. A girl who tries to do it all and doesn't let her CP get in the way of life. She just goes with it!

Operated on as an infant, without anesthesia, Wendy P. Williams began life at war with her body. There were tubes everywhere, in and out of every opening, her mother reminded her on every anniversary of her surgery. Autobiography of a Sea Creature takes listeners on Williams’ difficult sensory journey toward healing, as she communes along the way with horseshoe crabs, dolphins, and other marine life that taught her the restorative power of beauty, resilience, and interdependence.

Three months into her pregnancy with her first child, Hilary Yancey received a phone call that changed everything. As she learned the diagnosis - cleft lip and palate, a missing right eye, possible breathing complications - Hilary began to pray in earnest. Even in the midst of these findings, she prayed that God would heal her son. God could do a miracle unlike anything she had seen. Only when Hilary held her baby, Jack, in her arms for the first time did she realize God had given her something drastically different than what she had demanded.

Born four weeks premature and weighing little more than five pounds, Scott A. McCreight had a rough start and uncertain future. He was placed for adoption, but the good news didn’t last long: shortly after, Scott was diagnosed with cerebral palsy. Developmental delays permeated his childhood, the odds for a “normal” life seemingly stacked against him.

A revelatory collection of essays on the DeafBlind experience, and a manifesto on the power and untapped potential of touch. Born Deaf into an ASL-speaking family and blind by adolescence, John Lee Clark learned to embrace the possibilities of his tactile world. He is on the frontlines of the Protactile movement, which gave birth to an unprecedented tactile language and a way of life based on physical connection.

Le 8 décembre 1995, à la suite d’un accident vasculaire cérébral, Jean-Dominique Bauby est plongé dans un coma profond. Quand il en sort, toutes ses fonctions motrices sont détériorées. Atteint de ce qu'on appelle le " locked-in syndrome ", il est littéralement enfermé à l'intérieur de lui-même ; il ne peut plus bouger, manger, parler ou même simplement respirer sans assistance. Dans ce corps inerte, seul un œil bouge.

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 story of one man’s experience of a major stroke and his attempts to recover from it ….. but, enough of that - this is also an account of a dog’s experience of life with unpredictable, irrational human beings and his attempts to deal with all of that.

Emily Owen was a highly intelligent teenager who was also athletic and a skilled musician. Tragically, in her late teens she was diagnosed as suffering from Neurofibromatosis Type 2 (NF2). Since then, Emily has survived many complicated surgical procedures, been close to death, and seen the gradual erosion of all the abilities that defined her personality including the total loss of her hearing. Despite this, she has a remarkable sense of humor and has coped with everything she has been through due to her strong Christian faith, her supportive family, and indomitable personality.

Told with shocking honesty and in unbelievable detail, Bipolar: A Gift of Thorns is a profoundly insightful memoir that shines a light on one woman’s courageous journey and the stigma of bipolar disorder.

In 1895, a specialist straps five-year-old Katharine Hathaway, then suffering from spinal tuberculosis, to a board with halters and pulleys in a failed attempt to prevent her from becoming a “hunchback” like the “little locksmith” who does odd jobs at her family’s home. Forced to endure her confinement for ten years, Katharine remains immobile until age fifteen, only to find that none of it has prevented her from developing a deformity of her own.

Born without arms or legs below his elbows and knees, Kyle Maynard excels as a champion athlete, inspirational speaker, college student, and male model. No Excuses is his inspirational autobiography that shows how a positive, can-do attitude gives someone we might see as disadvantaged the advantage over life.

Greg Marshall's early years were pretty bizarre. Rewind the VHS tapes (this is the nineties) and you'll see a lopsided teenager limping across a high school stage, or in a wheelchair after leg surgeries, pondering why he's crushing on half of the Utah Jazz. Add to this home video footage a mom clacking away at her newspaper column between chemos, a dad with ALS, and a cast of foulmouthed siblings.

Have you ever been around people, yet still felt alone? Dr. bird has too. Within the first variant of their envirusmental series, they revealed thirty years of their late-in-life realized secrets. In this second volume, they, literally and figuratively, Zoom in on the last four "unprecedented" ones. This includes them cutting-the-s--t about how, half-way through their PhD, COVID-19 hit. And how, a couple years later, they added "Dr." to the front of their nickname.

How Being a Nomad Saved My Life is the true story of Debra Dickinson and her journey through navigating a grim traumatic brain injury diagnosis, where she was told she wouldn’t make it to 2016, to thriving and living life on her own terms while being on the road as a full-time nomad. She gives you glimpses into her life: the ups and downs, the hardships and scary moments on the path she has taken to live authentically in every way possible while on the road. As you listen to her experiences, you’ll be inspired to find your own truth and to never give up, no matter what.

One September day in 1955, Rita’s life changed forever when polio struck her family. She was five years old. Rita became totally paralyzed; her brother was partially affected, and she lost her mother to the virus. The hospital became her home, and the ward sister her mother. Hospital life was harsh in the 1950s: Crying was a punishable offence and meant solitary confinement. Rita struggled to walk again using leg callipers and a spinal brace, and later became mobile with the use of a wheelchair.