Disability Biography

This is a story about a mother and son on a road trip along the Pacific Coast of Southern California. Asher is a 19-year-old child/teen/man who is diagnosed with severe cerebral palsy and a visual impairment rendering him nonverbal, wheelchair bound, and visually impaired. Stacey is his devoted mother and a neuropsychologist who specializes in the assessment of children with neurodevelopmental disabilities.

When Joanne Jacobson’s writing about her mother’s respiratory illness was interrupted by her own diagnosis with a rare blood disorder, she found her perspective profoundly altered. Every Last Breath follows these two chronic illnesses as they grow unexpectedly intertwined. Rejecting a fixed, retrospective point of view and the forward-moving trajectory of conventional memoir, Jacobson brings the reader to the emotionally raw present - where potentially fatal illness and “end of life” both remain, emphatically, life.

Do you want to live? That’s the question Scott Fedor was forced to confront after he suffered a catastrophic injury while diving into a lake. His life forever changed in seconds. Facing the darkest and most debilitating days that nearly cost him his life on several occasions, Scott was determined to rekindle his spirit, ultimately discovering that the boldest of pursuits come in all shapes and sizes. Head Strong is a gripping tale of determination, perseverance, incredible faith, and human triumph that proves we are stronger than we realize.

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.

My wife Yash and I can vividly recall each moment related to the life of Maurya, our first-born. The arrival of our son Maurya on July 11, 2012, was a watershed moment for us. Everybody’s journey on planet Earth is different, yet there are commonalities in certain universal experiences that bind us together as a race with emotional chords.

In 1989, at the tender age of 12 years old, Ms. Meadows awoke from a coma to find herself suddenly struck blind and severely brain injured. This greatly complicated her young life. When she was yet a minor child, her mother sued the doctor who caused this tragedy. This ultimately made Ms. Meadows' situation more desperate than ever. After the settlement; Ms. Meadows' parents continued to deny her treatment for her injuries. As a result, her life went off the rails in a huge way.

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.

Hiroshima was one of the great tragedies of WWII. But out of the devastation of the first atomic bomb, some survivors emerged, 25 courageous Japanese women who became part of a remarkable humanitarian epic. Victims of the atomic blast that ushered in the Nuclear Age, these women were brought to the United States in 1955, where they underwent reconstructive surgery to repair the ravages of the bomb. Schoolgirls when the bomb destroyed their futures, they began to remake their lives and re-create themselves. This is the compassionate, often bittersweet chronicle of the Hiroshima Maidens.

I wrote this book to share with you; that I have cerebral palsy, but it does not define me. I hope you listen to this book; understand my challenges and successes. I live by these words “If I don’t take the challenge and do my best, I don’t taste success.” This book has short essays on the important events in my life. The chapters with poems is based on my feelings; what happens in my life.

Joe Secrist was born with a rare condition called coloboma, which means that part of the one or more structures inside an unborn baby’s eye does not fully develop during pregnancy. A coloboma occurs in about one in 10,000 births. He was not diagnosed until his early childhood and was considered the clumsy boy who crashed his bike. This is Joe’s story and his account of life during his years of abuse and neglect. Once sent away, his abuse continued at the Indiana School for the Blind. Joe has kept his silence until now.

Lionheart is an inspiring story of love, forgiveness, and the power of music. On April 27, 2016, while riding his bicycle in Nashville, Tennessee, David was hit by a distracted driver. Doctors told him he would never walk again. His life had changed forever. Lionheart is the richly detailed and intimate account of David's crash, recovery, and return to music: From thinking he lost everything, to appearing on national television (twice), to marrying his soulmate, Kristi - to finding a life and purpose beyond his wildest imagination.

My Autistic Fight Song is a memoir that follows Rosie Weldon’s journey from a college drop out as she tries to achieve her dream of being a qualified accountant. With the odds stacked against her and the stakes high, she refuses to give up on her dream. Of two things Rosie was sure. First, she wanted to be an accountant. Second, she was destined to be alone. But when life threw at her an autism diagnosis and a mystery girl, she was left asking: Who would employ her and was she capable of falling in love?

When a devastating event takes away the way of life you are accustomed to, you have two choices: Stop living, or start planning! In this memoir, Shawn Paulsen demonstrates how he has overcome his stumbling blocks and turned them into stepping stones on his journey through the misfortunes of life. Shawn’s story inspires and motivates others to overcome. He describes how he has learned to face adversity with his chin up by taking a comedic view of his malady and life.

Not that anyone wishes to be paralyzed in a motorcycle accident, but tragedy set the stage for triumph and the making of a real life fairy tale. When the harsh reality of paralysis turned the dream of having a family together into a nightmare for Erik and Jennifer, they had to face their deepest fears and live courageously, because sometimes fairy tales are just stories of love's perseverance.

Inside My Outside: An Independent Mind in a Dependent Body provides an in-depth look into the life of a young woman with cerebral palsy who cannot walk or talk but who uses an electronic device for communication. This memoir covers three full days, from morning to night, in Sara Pyszka’s life, providing glimpses of past relationships, friendships, schooling, and outrageous stories about the challenges of hiring, firing, and working with personal care assistants.

Do you know an adult with autism, Down syndrome, or another special need? One in eight people on our planet live with some form of disability. And they all deserve to live productive, engaged lives. Are we willing to help them accomplish this goal? The mother of an adult with autism, Andrea Moriarty leveraged her son’s passion, talent, and personality to help him create an out-of-the-box vocation: A podcast. After more than 80 interviews, she recognized three vital attitudes that people with disabilities teach us - risk taking, humility, and kindness.

Jordan’s traumatic birth caused brain damage, whose limits he refused to accept. He embraced every struggle, learned to work through his weaknesses, and ultimately, redefined himself despite his learning disability label. All thanks to his dedicated cheer squad - family, friends, and God - he knows his potential has no limits, except those he puts on himself. But that doesn’t mean he’s escaped significant hiccups and challenges along the way.

Bárbara Anderson narra con brutal franqueza el día a día de tener un hijo con discapacidad: los retos dentro y fuera de casa, las complicaciones de salud y de vida; los cambios de prioridades; el Everest de cada día al tener un hijo con - hasta ahora - un diagnóstico irreversible como es la parálisis cerebral infantil.

For Magda Newman, normal was a goal—she wanted her son Nathaniel to be able to play on the playground, swim at the beach, enjoy the moments of childhood that are often taken for granted. But Nathaniel's severe Treacher Collins syndrome—a craniofacial condition—meant that other concerns came first. Could he eat without the aid of a gastrointestinal tube? Could he hear? Would he ever be able to breathe effortlessly?

Normal. Who is to say what this word means? For Magda Newman, it was a goal. She wanted her son Nathaniel to be able to play on the playground, swim at the beach, enjoy the moments his friends took for granted. But Nathaniel’s severe Treacher Collins syndrome - a craniofacial condition - meant that other concerns came first. Could he eat without the aid of a gastrointestinal tube? Could he hear? Would he ever be able to breathe effortlessly? But Nathaniel looks at “normal” from a completely different perspective.