Disability Memoir

This is the biography of a young man with some neurological differences, written in the first person. Through his eyes, we see how he perceives his life and negotiates his reality. His world and his understandings of life may be different from the norm, but we learn to appreciate a special type of soul that should be acknowledged and celebrated as part of human diversity. This book demonstrates the love and nurturance of his mother and the dynamics of his relationship with her. We also enjoy hearing about the comfortable lifestyle that Marcelo has been given, including his worldwide travels.

Elaine Asato conta como reinventou sua vida após perder quase totalmente a visão aos 29 anos. Guiada pelo conceito finlandês SISU - força, coragem e persistência -, tornou-se referência em liderança e desenvolvimento humano, impactando milhares de pessoas. Porque a verdadeira força não está em um único impulso diante do desafio, mas na coragem de seguir, se transformar e viver uma vida autêntica e extraordinária.

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.

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!"

While society called his disability an obstacle and limitation, Neil argued that his "flourishing dystonia" allowed him to think, explore, and create art in a way most people cannot. True to his words, Neil embraced every opportunity to experience life to its fullest, from navigating the Alaskan wilderness in a wheelchair to commanding the spotlight on stage. In this deeply personal account, Neil invites listeners into his world as he remembers adventures and escapades, triumphs and disappointments.

They were part of the Baby Boomer vanguard, three boys thrown together in a 1950s Southern California subdivision looking like most other boys of that era. Under coonskin hats they ran free all summer long inventing their own games and endless challenges, fought imaginary Indians and pirates in a nearby orange grove, and on occasion battled a neighborhood bully or two. Their greatest enemy, however, was an infectious disease called polio – a paralyzing scourge that maimed and too-often killed little kids.

Families who have supported a child with special needs will connect with this memoir about Sarah, a feisty girl with autism and a unique genetic blueprint. Her mom, Jenny, is equally feisty and determined, which leads her to make a commitment that dramatically changes her and Sarah’s lives—as well as those of many others.

Lass dich inspirieren – von kraftvollen Geschichten aus dem wahren Leben! Es sind Geschichten, die von tiefen persönlichen Krisen handeln, die berühren und auf einzigartige Weise inspirieren. Katharina Afflerbach verwebt die Lebensgeschichten mit ihren eigenen Erfahrungen und Schicksalsschlägen und leitet davon kraftvolle Strategien ab, wie Menschen sogar in den schwersten Momenten neue Zuversicht schöpfen und über sich hinauswachsen können. Sie zeigt, dass Zuversicht viel mehr ist als Hoffnung: ein aktiv beschrittener Weg, sich selbst auszurichten, aufzurichten und dem Leben zu begegnen.

This memoir combines the drastic losses which occur due to severe episodic memory deficits with the greater agency currently afforded to all of us as made capable via ingenuity and technology. In this book memory loss is considered within the present-day environment of novel solutions heretofore unimaginable. All of us may never need to worry about recalling key life events ever again.

In "You're Not Doing It Right," Ellen Patnaude bravely opens the door to the haunting reality of Lewy body dementia (LBD) and unravels its profound impact on families. One of the most common types of dementia after Alzheimer's disease, LBD is marked by fluctuations in cognition, hallucinations, and motor symptoms. The journey begins with subtle warnings of small changes in her mother's behavior that worry Patnaude's father, but go unnoticed by the author and her sibling.

Stroke of Love is the life story of a young stroke survivor from Texas named Hether Flanigan. It is a story of resilience, determination, strength, and love. A story about the human spirit, the will to live life to the fullest, the power of the human mind, and the love that surrounds us.

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.

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.

Darryl Jefferson was diagnosed with Asperger's syndrome at the age of eight and encountered many hurdles in life due to the condition. Despite this, he persevered through many challenges in school, work, relationships, and the military. In this story, he takes us on a journey through one man's experience of living with autism and its effects on school, work, relationships, friendships, and many other life challenges.

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.

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.

At the age of sixty, and having lived with Parkinson’s disease for over ten years, Guy Deacon CBE set out on one last adventure: to drive solo from his home in the UK 18,000 miles and through twenty-five countries to Cape Town on the southern tip of Africa. This incredible journey, across Europe and down the full length of Africa, took the former British Army officer over twelve months. Along the way, he broke down five times, underwent one emergency evacuation, and took 3,650 prescription pills.

Martin Hibbert was left paralysed from the waist down by the Manchester Arena bombing which killed twenty-two people on 22 May 2017. Martin’s teenage daughter Eve was one of the 940 injured, in Eve’s case, gravely. The dad from Bolton has since become a leading campaigner both for victims of the atrocity and those with spinal cord injuries. Determined to make a difference he took on the ultimate challenge, scaling Kilimanjaro in a wheelchair, becoming the second paraplegic to do so, and raising a million pounds for charity.

Carly-Jay Metcalfe was born with cystic fibrosis, survived a double-lung transplant at the age of 21 and faced a rare cancer at the age of 30. What she has endured should have killed her, but her humour, courage and optimism became her best survival skills. From her hospitalised childhood to her many friendships, loves and losses, Metcalfe shares the fickle nature of life with candour and warmth. She writes with compelling insight about organ donation, opioid addiction and survivor's guilt, while still managing to find joy amongst the wreckage.