Disability Memoir

You struggle with your disability. You're tired of being counted out of life. Are you frustrated because you feel, or have been told, you can't be 100% healthy with your disability? It's time for a change! It's time to prove everyone (including your doctors) wrong! Author and certified personal trainer Tony Jacobsen, who has Osteogenesis Imperfecta (Brittle Bones Disease), has transformed his entire life and now shares the formula to empower other people with disabilities.

Es ist Nicoles zweiunddreißigster Geburtstag, als sie unter der Dusche steht und sich auf die Feier mit ihren zwei kleinen Kindern und ihrem liebevollen Mann freut. Abrupt wird sie aus ihren Gedanken gerissen, als sie einen Knoten in ihrer Brust ertastet. Eine Welt bricht für sie zusammen. Später stellen die Ärzte die Diagnose, dass in Nicoles Körper nicht nur ein hochaggressiver Tumor wächst, sondern dass sie außerdem dieselbe genetische Vorbelastung wie Angelina Jolie hat. Selbst nach erfolgreicher Therapie, bleibt die Wahrscheinlichkeit einer erneuten Erkrankung enorm hoch.

Born deaf and discovering encroaching blindness at the age of 16, Anthony Lawton’s future appeared to be full of locked doors. Prejudice. Delayed education. Distorted speech. Limited sight. But when benign strangers intercede and inner gifts reveal themselves the opportunity to pursue a childhood dream of speaking and participating in mainstream society become a realisable vision. He would need to do this before the consequences of dual sensory loss would again close the doors.

Blind Vision is a fascinating account of a unique and inspiring career in open-water swimming. But more than that, it is a story for anyone that’s ever been told they can’t. James Pittar is living proof that no matter what the odds, with dedication, passion, and the right people around you, you can.

Our Life Our Way: A Memoir of Active Faith, Profound Love and Courageous Disability Rights explores an extraordinary love story grown out of engagement with both disability rights advocacy and christian faith communities. This memoir contains thoughtful, often entertaining, and sometimes heart-wrenching anecdotes of a couple’s journey to create their profound relationship and Christian marriage, in a world not yet ready for them.

Adventurous international teacher, Amy Bovaird, is diagnosed with Retinitis Pigmentosa, a hereditary eye disease that will blind her. In spite of that, she manages to continue teaching overseas. Then her father's final illness brings her back home for good. There, friends and acquaintances begin to notice that she doesn't always recognize them and sometimes stumbles as if drunk! Insensitive students ridicule her in the classroom.

My name is Joseph A. Peragine. I am a paranoid schizophrenic. On October 22, 2000, I tried to kill myself in a severely hallucinogenic state due to undiagnosed paranoid schizophrenia. I was suffering from this illness for many years leading up to that day. Every October since I started my recovery in 2000, I reflect on my life and am extremely thankful that I was fortunate enough to have been given a second chance.

I know this sounds a bit cliche, but life truly is a journey. It evidences as a unique sojourn for every individual person. This is the story of a child born seventy years ago. It is a story of triumph and setbacks, of joy and sorrow, of weakness and strength. But most of all, it is a story of courage. Brian J. Woznicki was born with cerebral palsy. He was dealt a very difficult hand in life.

We treat the body as an afterthought, until it no longer can be. Until the pain or the pleasure is too great. Sinéad Gleeson's life has been marked by terrible illness, including leukemia and debilitating arthritis. As a child, she bathed in the springs of Lourdes, ever hopeful that her body would cooperate, ever looking forward to the day when she could take her body for granted. But just as she turns inward to explore her own pain, and then the marvel of recovery, and then the arrival of her greatest joys—falling in love, becoming a mother—she turns her gaze outward.

Everything happens for a reason; I truly believe writing these words was one of the primary purposes of my life. Father God gave me this disability - I’m just trying to make the most out of it. This is not your typical autobiography or memoir. I’m sharing my life experiences as more of a commentary on humanity as a whole. I do my best to sprinkle bits of comedy throughout the composition so it feels more like a conversation between friends than me just talking at you.

I matti ci incuriosiscono, ci costringono a riflettere, ci cambiano lo sguardo, ci mettono davanti ai nostri fantasmi, non ci lasciano mai indifferenti. La storia dell’uomo è costellata di individui eccentrici, bizzarri, anticonformisti, visionari, in molti casi con disturbi psichici gravi, ma altamente creativi in campo letterario, artistico, scientifico. Partendo da queste considerazioni, è nata l’idea di una sorta di calendario che racconti, al posto del santo del giorno, il matto del giorno.

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.

An ambulance rushed her away to the emergency room at a local hospital. Her life was forever changed in that moment. In this powerful memoir and inspirational self-help book, Kimberly Muka Powers shares her triumphant story of living with bipolar type one disorder with psychotic features. Humbled by this life-altering mental health diagnosis, she learns to rise above the setbacks of her illness and empowers others to do the same.

At the age of four, Joshua Miele was blinded and badly burned when a delusional neighbor poured sulfuric acid over his head in a crime that shocked New York. It could have ended his life, but instead, Miele—naturally curious, and a born problem solver—not only recovered, but thrived. Throughout his life, Miele has found increasingly inventive ways to succeed in a world built for the sighted, and to help others to do the same. At first reluctant to even think of himself as blind, he eventually embraced his blindness and became a committed advocate for disability and accessibility

I Kept Walking opens in 1940s Tehran when a misguided prank leaves three- year-old Minou frozen in fear. Days later, a doctor breaks the news to her mother: "Your daughter has polio." To understand why nothing is as it seems-the cause of her polio or why her dutiful Jewish mother, who was married off at 13, thwarted her dream of marriage, Minou must flee Iran and confront the psychological toll of her polio. I Kept Walking is the audacious account of a bold young woman who was unwilling to be crushed by polio or the prohibitions of a conservative society.

Left partially paralysed below the rib cage by polio, Anne Wafula Strike was forced to flee her native Kenyan village, moving across the country with her family. After overcoming additional adversity, including the loss of her mother and ableist prejudice, Anne moved to the UK, where she discovered her talent for wheelchair racing. The first East African to compete in her sport, representing Kenya in the 2004 Paralympics before joining Paralympics GB, Anne is now a fierce advocate for the promotion of the games around the world, and a champion of disabled rights.

In the depths of despair, contemplating suicide, I gazed out a rain-streaked window in Maryland, where blurred colors in a parking lot mirrored my shattered soul. The shame of being sexually abused haunted me with recurring nightmares and PTSD, leading to a life cloaked in a complex facade of military titles and untold secrets. In this powerful memoir, published poet and author Adam Volant shares his raw and inspiring testimony of overcoming unimaginable brokenness to achieve success.

Wie können wir Inklusion endlich umsetzen? Eine so persönliche wie politische Geschichte. 2016 wird Hadija Haruna-Oelker Mutter eines behinderten Kindes. Immer wieder trifft sie auf Barrieren und trennende Systeme, die seit Jahrzehnten bekannt sind: Bürokratie, pseudoinklusive Schulen oder unhinterfragte Diskriminierungen und Abwertungen im Alltag.

Carla Sosenko was born with Klippel-Trenaunay Syndrome, a rare vascular disorder that resulted in legs of different sizes, a mass of flesh on her back,­­ a hunched posture, and other idiosyncrasies big and small. She spent years trying to hide under layers of clothing, and then experimented with the opposite: wearing tiny dresses and short shorts, daring people to stare so she could make them regret it. No matter what she did, she was worried that she didn’t measure up.

Ruth's tribe are her lively children and her filmmaker husband, Simon, who has motor neurone disease and can communicate only with his eyes. Ruth's other tribe are the friends who gather at the cove in Greystones, Co. Wicklow, and regularly throw themselves into the freezing cold water just for kicks. The Tragic Wives' Swimming Club, as they jokingly call themselves, meet to cope with the extreme challenges life puts in their way, not to mention the monster waves rolling over the horizon.