Showing titles in People with Disabilities

Mehr als nur ziemlich beste Freunde... Mit 16 erleidet Justin einen Verkehrsunfall, der ihn fast tötet und eine langsam voranschreitende Autoimmunerkrankung auslöst. Er kann seine Arme und Beine nicht mehr bewegen, ist auf den Rollstuhl angewiesen. Sein Traum: den Jakobsweg gehen. Als er seinem Freund Patrick davon erzählt, zögert dieser nicht, sich mit ihm zusammen auf das Abenteuer einzulassen. Sechs Wochen sind die beiden unterwegs, die Reise bringt beide an ihre Grenzen, doch gemeinsam bewältigen sie die 800 Kilometer über Stock und Stein durch Nordspanien.

In 1991, at the height of the Somali civil war, 12-year-old Abdi Warsame ran for his life through the streets of Mogadishu. In a flash, his legs were paralyzed and his cousin killed. With his country literally falling apart around him, Abdi had little hope for recovery. But, with his faith, his family, and his indomitable spirit, Abdi pursued every available route for a better life.

Autism and BPD are two conditions that affect every aspect of my life. I wouldn't be who I am if I were not autistic and did not have BPD. Within this book, you will listen to the struggles I've had to go through, from growing up, to confusing teenage years, to challenges in adulthood. You will also listen about the good times I've had in my life, and my reasons for carrying on when I was at my lowest. Some of the content within this book may be triggering, but if it helps just one person, it would have been worth it. I hope you enjoy listening to my story.

Hannah Diviney has always known that her experience of the world was fundamentally different from those around her. While her friends went to soccer and dance and little athletics, Hannah was going to physio and doctors' appointments. While her friends got jobs, fell in love and went clubbing, Hannah surrounded herself with the fantastical worlds she found in books. But books where people like her were nowhere to be found. Refusing to accept the narratives, or lack thereof, that she'd been given, Hannah was determined to forge her own path in a world that wasn't designed for her.

Shock. That was Darla's first reaction when her carefree childhood was disrupted by cancer. Her life became a roller coaster of intense emotions. Sadly, she lost her leg and, ultimately, faced death. During her illness, we shared difficult times, but also great times celebrating life as Darla grew in faith and joy. She lived in the present (not worrying about her past or future) and was very positive. Darla was a joy to be with because she was joyful!

This book is about the life of the author. It focuses on her faith, her hope, and her endurance during the years of her illness. In this true story, you will learn the how and why about the effects that changed her family’s life—the author’s Crohn’s disease, the 14 blood clots, toxic gut syndrome, colitis, tumors, ulcers, vertigo, weight gain and loss, pregnancies, the many surgeries, and how her body would not wake up after some of her surgeries.

Why the Cane? is a personal memoir which recounts the true story of a man’s regaining a level of activity he thought would not be possible after a devastating injury. It chronicles his medical journey, the upheaval suffered by his family, and the counsel and support which shifted his focus and provided a framework to make thoughtful decisions for the long term.

As a US Army infantryman in World War II, Don Wedewer was twice wounded in four days. On both occasions, he was left for dead. Now he was a double amputee and blind with seemingly no hope for the future. Yet through extraordinary determination and persistence, this highly decorated combat veteran overcame seemingly impossible odds to become a state and national leader in providing opportunities for those with visions loss. This is Don Wedewer's story. For more information visit www.bravestguy.com.

For 20 years, Lisa Murphy, Jeff Murphy, and a group of volunteers traveled the world with the Mobility Project, delivering mobility to the poorest people on the planet. They helped tens of thousands of disabled poor to gain mobility and hope. The disabled received wheelchairs, walkers, and crutches from the United States, items they never would have been able to afford. Like Simon of Cyrene, we helped people carry their cross of disability. From the hot tropical jungles of Costa Rica, Thailand, and São Tomé to the deserts of Afghanistan, the disabled poor got a new chance at life.

Tales from my Yellow Room is a first-hand account of the challenges of living with a congenital disability, and the invisible difficulties society adds to such a life. Written with candor and humor, this Scottish-American story may change people’s perception of disability.

After two decades of suffering with the mental disorder known as obsessive-compulsive disorder, Derek has reached his breaking point. His past attempts to find inner peace had lead him astray. At last he longs for a life of ease and tolerance without the handicap his illness brings. Enter the next phase of his life as he copes with obstacles ahead in this true story. Follow his path to recovery as he seeks help, wisdom, and clarity to rise above what has grounded him for so long.

Als Matt Haig mit 24 Jahren urplötzlich krank wird, begreift er nicht, welch dunkle Macht da von ihm Besitz ergreift. Die Krankheit überfällt ihn auf so dramatische Art und Weise, dass sie ihn buchstäblich an den Abgrund bringt. Doch Haig entscheidet sich für das Leben - und für seine große Liebe Andrea. Er findet heraus, dass er nicht allein ist mit der Diagnose Depression, sondern dass Millionen Menschen auf der Welt sein Schicksal teilen.

We were walking this journey together, yet alone. Two siblings from a close-knit, boisterous family of six. There is nothing like the camaraderie of family to give you the determination to persevere in spite of any obstacle. We were overwhelmed by the disease of multiple sclerosis as well as other autoimmune diseases. Our outward appearance of healthiness was deceiving. Unbeknownst to us, the disease of multiple sclerosis would eventually consume mobility, sight, memory, fine motor skills, speech, and so much more.

From childhood stutterer to inspirational speaker! The Courage to Shine is a powerful and inspirational memoir by Eileen Forrestal, a former anesthesiologist who transformed her life. After a lifetime of "putting people to sleep", Eileen is now in the business of "waking people up" as a writer, speaker, and coach. In The Courage to Shine, Eileen retraces her journey. She shares her childhood trauma of an accidental overdose of junior aspirin that led to her subsequent speech impediment, the embarrassment of which caused her to hide her voice in silent shame.

Have you ever wondered how a blind person pours a cup of coffee? Or how they and their guide dog know when it's safe to cross a busy road? When Lois Strachan lost her sight at the age of 21 years, she had to learn the answers to these and countless other questions of how to live as a blind person in a sighted world. In this delightfully quirky and entertaining book, Lois shares some of the secrets she discovered about how to live an “ordinary” life in an extraordinary way despite her disability.

A little over a year of living with bipolar type one. I ended a year off of medications deeply in love and with a stay in jail for joy-riding and fleeing and eluding. My family suffered, my friends suffered, and I suffered. This is a journal starting after my stay in jail. I respond to the journal entries all the following year, surprised mostly by the degree of my mental illness. This is not a self-help audiobook, and I struggle most of the time, not really coming up with many good solutions to my issues. Nothing about the past couple years has been easy.

See? is an inspirational autobiography that describes how God's grace and the firm, loving support from family, friends, neighbors, an exceptional teacher, and caring supervisors guided the author through life's challenges. It also debunks common myths of blindness and discusses adaptive equipment used by the author on her journey.

2020 was a hard year for everyone. In this journal, learn how one woman experienced the pandemic while also having to deal with the effects of having bipolar disorder. From the book: "Truth is best expressed as silence. Words are our creations. They come and go, live and die. They are incapable of expressing what is real. This has been a journal of a false identity assuming itself to be real. From this new vantage point, I see how I am creating this story. Today I start a new chapter. Or maybe it is just a page. Even if I could just cobble together a sentence. Make it meaningful!"

This book will bring you inside of the psychotic experience of someone living with autism. As usual, this story is told with no filter and comes from the heart of an aspie, making it a valuable tool in understanding the co-morbid issues a person with autism might face when encountering psychosis.

I have always had difficulty seeing. It started as a child with difficulty seeing at night. Never in my wildest dreams did I think I would one day be diagnosed with a rare condition that could eventually take my vision completely. This book touches on some of the struggles I, and others suffering with visual difficulties, go through. It is my hope this will give an understanding to others and help those dealing with their own issues to find peace knowing they are not suffering alone.