Zeigt Titel in Menschen mit Behinderung

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.

Frank Rivera is an advocate for not only Sarcoidosis, but also for the rare disease and chronic pain community. This audiobook is about how to rise above adversity and the strength of one person. One person can make a difference if you work hard. Frank has dealt with adversity as a child with leukemia. His mother having health issues herself taught him strength and love. He fought through tough times during his childhood to only find out as an adult, after misdiagnosis, he has a rare disease that has no cure.

My audiobook is about Aden and his journey and his constant battle in life, from childhood to his adult life. The story of how he struggled for years unaware of his dyslexia or his Scotopic Sensitivity \ syndrome until he was fully assessed at the age of 40. This audiobook seeks to inspire others to understand dyslexia and to help them face criticism and discrimination. Over the years, Aden had to overcome insurmountable obstacles in life. His determination to succeed came from these very rejections and insults.

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.

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.

Heather M. Dakin has been legally blind since birth, but that hasn’t stopped her from making the most of life. Observations of a Blind Magician chronicles Heather’s journey - from becoming a white-cane user and later a guide-dog traveler, to her move from the United States to the United Kingdom in 2009. She highlights the challenges blind and visually impaired individuals face in various arenas of life with a touch of good-natured humor. Her story offers a new perspective on a world that few individuals ever get to see.

Meet Priscilla and Dave — two headstrong people with very different but complementary disabilities. When they met, fireworks flashed, but they soon became inseparable and each other’s "other half". Together, they attacked and overcame every obstacle in their way — and had one hell of a time doing it. Follow the story of their fiery love affair among moments of raucous laughter, fear, joy, sadness, and incredulity at people's behavior.

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.

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.

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.

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.

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.