検索キーワード： 障害者

Learn about narcolepsy and one persons struggle living with the disease before and after diagnosis. Have you ever woke up and not known where you were or how you got their? You may have narcolepsy. Have you ever laughed so hysterically you fell down motionless? You may have cataplexy. Have you ever been accused of being drunk or on drugs, even though you know you were not?

From the steel town of Scunthorpe to the Steel City of Sheffield, Bill’s life demonstrates the importance of perseverance and faith as he tells his personal story of loss and hope, with the aim of inspiring others who are struggling with the situations life throws at them. Anyone who reads this book cannot fail to be struck by the uniqueness of it, nor by how the author’s Christian faith carried him through - literally - the darkest of times. Now I See is truly an inspirational book.

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.

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.

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.

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.

Axel Schylströms självbiografiska "BRÄND" är en handbok i motivation och mental styrka. Som nittonåring brännskadades Axel med tredje gradens brännskador över 70% av kroppskostymen. Ofrivilligt fick han spendera över ett års tid av intensiv fysisk och psykisk rehabilitering för att överleva. Trots ärren, handikappen och den ständiga motvinden kunde ingenting stå i vägen för Axels dröm om att bli artist, och idag är han en av Sveriges mest folkkära pop-hopp.

Selbstwert genießt einen guten Ruf, das sogenannte Ego keineswegs. Es wird selten geschätzt, allenfalls geduldet. Janis McDavid wirft einen anderen Blick auf das stets im Narzissmusverdacht stehende Ich. Tragfähige Selbstwertschätzung, aber auch Empathie brauchen ein Ego. Das Hörbuch zeigt anhand der persönlichen Geschichte des ohne Arme und Beine geborenen Speakers, welche Wege und Mittel ihn zu einer gesunden und stabilen Selbstwertschätzung brachten.

Nach seinem Besteller "Setze dir größere Ziele!" beleuchtet Zitelmann in seinem neuen Buch wieder ganz ungewöhnlich erfolgreiche Menschen: Persönlichkeiten, die trotz Behinderung geradezu Übermenschliches geleistet haben: Ein Blinder, der die 7 höchsten Gipfel der Welt bestiegen hat, ein Weltreisender, der schon vor 200 Jahren blind 400.000 Kilometer zurücklegte, ein Motivationsredner ohne Arme und Beine, eine erfolgreiche Unternehmerin im Rollstuhl, eine Schriftstellerin - taubstumm und blind - und ein weltberühmter Schauspieler mit Parkinson.

La forza necessaria per superare i nostri limiti è già dentro di noi. L'importante è non perdere di vista l'obiettivo finale. Questa è la storia di un ragazzo molto speciale. Ma è anche la storia di un ragazzo come tutti gli altri, che deve crescere e imparare ad accettarsi così com'è, ad aprirsi e a farsi voler bene, a superare i momenti difficili e ad apprezzare la meraviglia di ogni giorno. E scoprire che, a volte, avere il vento contro è proprio quella condizione ideale che ti fa venire voglia di volare. Questo ragazzo si chiama Daniele, ed è cieco dalla nascita.

Trente-deux ans, c'est le nombre d'années qu'il m'a fallu pour mettre un nom sur ma différence. Comment ai-je pu "passer au travers des mailles du filet" durant tout ce temps ? Je vous révèle, au travers de ce récit parsemé d'anecdotes, comment j'ai grandi dans l'ignorance de mon syndrome. Plongez dans mon quotidien et découvrez chacune des étapes clés de mon évolution ainsi que les moyens mis en œuvre pour survivre dans ce monde parfois difficile à appréhender.

Clem Bastow grew up feeling like she’d missed a key memo on human behaviour. She found the unspoken rules of social engagement confusing, arbitrary and often stressful. Friendships were hard, relationships harder and the office was a fluorescent-lit nightmare of anxiety. It wasn’t until Clem was diagnosed as autistic, at age 36, that things clicked into focus. Clem reflects as an autistic adult on her formative experiences as an undiagnosed young person, from the asphalt playground of St Joseph's Primary School in Melbourne to working as an entertainment journalist in Hollywood.

So begins Chloé Cooper Jones’s bold, revealing account of moving through the world in a body that looks different than most. Jones learned early on to factor “pain calculations” into every plan, every situation. Born with a rare congenital condition called sacral agenesis which affects both her stature and gait, her pain is physical. But there is also the pain of being judged and pitied for her appearance, of being dismissed as “less than.”

As a deafblind woman with partial vision in one eye and bilateral hearing aids, Elsa Sjunneson lives at the crossroads of blindness and sight, hearing and deafness—much to the confusion of the world around her. And she knows how wrong our one-size-fits-all definitions of disability can be. Part memoir, part cultural criticism, part history of the deafblind experience, Being Seen explores how our cultural concept of disability is more myth than fact, and the damage it does to us all.

At once heartbreakingly honest and strikingly witty, Holding On by Letting Go is the unforgettable true story of one woman's journey through despair to acceptance and hope. Ultimately, it is a portrayal of the light that can be found in the darkest of times.

Robert Mercer's life could have been very different. He was born with very low vision and as a youngster struggled in school. But through the intervention of a caring teacher and the support of his family, he found his way to the Halifax School for the Blind and into the classroom of Mrs. Beaton. It was there he discovered his voice, a voice he uses to recount his remarkable journey from a shy little boy to a community leader.

Having grown up on their great-grandfather’s stories, Royd Tolkien and his brother, Mike, have always enjoyed adventures. So when Mike is diagnosed with motor neurone disease, also known as ALS, the brothers decide to use the time they have left to tick off as much as possible from Mike’s bucket list, from remote camping in Norway to travelling through Royd’s beloved New Zealand. Yet, when Royd loses Mike, he discovers his brother had been writing another kind of bucket list: 50 things he wanted Royd to do after his death.

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.

At the age of 27, Whitney Dafoe was forced to give up his life as a photographer who traveled the world. Bit by bit a mysterious illness stole away the pieces of his life: First, it took the strength of his legs, then his voice, and his ability to eat. The Puzzle Solver follows several years in which he desperately sought answers. Whitney's father, Ron Davis, PhD, a world-class geneticist at Stanford University whose legendary research helped crack the code of DNA, suddenly changed the course of his career in a race against time to cure his son's debilitating condition.

On July 4th, 2013, Connor Sparrowhawk, also known as Laughing Boy or LB, was found dead in a specialist NHS unit. Connor, who had autism and epilepsy, had a seizure while in the bath, and no member of staff was on hand to stop him from drowning. An entirely preventable death. Sara Ryan presents a frank, sometimes funny and touching account of her son's early life and preventable death and the unfolding #JusticeforLB campaign.

Diagnosed with pathological demand avoidance (PDA) in his teenage years, Harry Thompson looks back with wit and humour at the ups and downs of family and romantic relationships, school, work and mental health, as well as his teenage struggle with drugs and alcohol. By embracing neurodiversity and emphasising that autistic people are not flawed human beings, Thompson demonstrates that some merely need to take the 'scenic route' in order to flourish and reach their full potential.

Hey guys, you might know me already from one of my social media channels where I talk about the highs and lows of living with Tourette's syndrome. I've loved sharing those times with you and - as there are lots of things I can't fit into a 60-second video - I've decided to write a book! It's the full story of how I came to be diagnosed and how having Tourette's has changed my life. Writing it has given me an opportunity to talk about things I haven't felt ready to share before - for some reason it's easier to put down private things in written words than in a video!