Showing titles in People with Disabilities

Shot point-blank in the side of the neck, Michael Kiel was completely paralyzed from the neck down on April 16, 1993. As a 19-year-old sophomore at Penn State - Altoona campus, the world he knew vanished. It was turned upside down and inside out, and the next four months in the hospital and rehab center would test every fiber of his being. This memoir is about his perspective on life - his entire life - before, during, and after a life-altering spinal cord injury.

A displaced person (now called refugee or economic migrant), aged 19, escapes in 1950 from behind the Iron Curtain with his mother's and her friends' help. He maneuvers through minefields and swims across icy waters and past Russian patrols to reach Salzburg and then Switzerland, hoping to catch up with his brother (who by then had migrated to Australia). He makes it back again, falls in love, but then emigrates to Canada to start a new life, gets to University in Toronto, and is then joined by his mother after escaping in 1956 during the Hungarian uprising.

Life is hard. Add in a disability, and it can be even more challenging. Tait knows. In My Name Is Tait, Tait writes about his successes, challenges, and hard times as he faces a world that doesn’t always accept his disability. In this book, you’ll have a front seat as Tait shares his thoughts on disability, family, education, work experience, and much more.

A journal-style book of what it's like to live with mental illness. Everyone is different, but this is how I experience mental illness every day.

An eight-year-old boy survives triple-limb amputation by freight train. One of America’s famous yet untold stories of overcoming the stigma of disability and responding with inspirational resilience. To change your perspective on life, listen now! Boy Interrupted takes the listener on Ricky’s remarkable journey of miraculous survival, the power of kindness, humor, mistakes, post-traumatic growth, and other surprises.

The book is an exciting true story filled with adventure and humorous anecdotes. The narrative starts by providing a background from earlier ancestors - through four generations. The author gives a unique account, beginning in Chipinge, located in Zimbabwe's eastern highlands. The villagers are confused by the ambiguous nature of how their ancestral land changed ownership.

This collection of poems was written from the day the author was sent to the emergency room through her first phase of radiation and chemotherapy treatment. Christina uses poetry to share her lived experience as a teacher, a patient, a psychologist, and a neurodivergent person. Kiss Your Brain: Diagnosis Diaries shares poems that fit under the categories of “on beautiful brains", “on resilience", and “on renewal".

Graham Hale Gardner died before turning 23 and never learned to walk or speak due to severe cerebral palsy complicated by epilepsy. Yet he left a legacy of love and compassion that deeply moved scores of people from widely different backgrounds. Graham’s story, written through the eyes of his father, speaks of the enormous legacy left by a boy who never spoke. A story that raises provocative questions about the “invisible lines of connection” that make us human.

The S Word is the raw and compelling true story of a girl coming of age raised by a mother with a mental illness, and who nearly suffocates in the silence she was taught to value above all else - until she finally finds the strength to break free of the secrets binding her and save herself. The S Word is a book for anyone who may be keeping secrets...for children too little to know they warrant a voice...for teenagers too confused to think they have a choice...for adults too overwhelmed to do what’s right.

Waste no day to achieve the impossible! When Pennsylvania started testing newborns for metabolic diseases, Adam Settle was one of the first to be diagnosed with Cobalamin-C Deficiency. Legally blind and mentally delayed, Adam never let his limitations hold him back from accomplishing his dreams. His love for people and his desire to help others comes through the sections of this audiobook. Whatever has been holding you back, this audiobook will help you charge through the obstacles you face to achieve the impossible. Adam’s story will inspire, encourage, and give you hope.

After three long years, Johnny’s young son, Sam, experiences a breakthrough. But even as calm comes to Sam's body, the illness makes off with his mind. Violent outbursts, strange obsessions - what has happened to his sweet boy? Cinematically weaving three generations of fatherhood, Remember, You’re the Greatest is a memoir of hard questions. Of unexpected joy in the ache of mystery. And the power of a special needs child to teach a father what greatness truly looks like.

Through his unique blend of good Scottish humor, real-life experiences, and funny stories of mishaps and misadventures, Iain M. MacLeod draws the listener into his vibrant life from childhood to the present - a life not defined by cerebral palsy, which he has had since the age of three.

Parenting can be a struggle, especially parenting a disabled child. In this flawlessly crafted memoir, Kramar describes championing her son, diagnosed with Sotos syndrome, through his short life. She examines the experience of loving and losing a child and reminds us that there is a way forward through the grief. Kramar’s memoir offers guidance, wisdom, and inspiration - an amazing story of redemption and hope.

After 30 years as a professor in the field of communication studies, Dr. Smith reminisces about some of his experiences and how his race and differently abled intersectionality have influenced documented encounters. As a Black and totally blind individual, he muses about how this distinction has both colored and shed light on what might have been innocuous or unremarkable encounters otherwise.

The day Ms. Meadows walked out of court victorious after her 15-year-long struggle to regain her Constitutional rights from the state of Montana and her four parents, she knew one thing for sure.... She would one day get even with the lawyers. After more than 30 years of this insanity, they have instead succeeded in creating a deeply passionate, intelligent, driven, broad-minded and crafty machine - a lady-genius with an unstoppable force. Ms. Meadows has mastered the secret of how to beat them. Join her as she embarks on this epic journey of Changing My Perspective.

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 she is 18, Hanneke Boot discovers that painting with her mouth is easier for her than painting with her hands. Born with a muscle disease, she’s experienced a host of challenges. But she’s found her calling in art and paints everything: views, landscapes, mills, and portraits. In Ain’t No Mountain High Enough, she shares her story. Boot narrates how being born with a physical disability guarantees you will run into obstacles for life.

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.

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.

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.