検索キーワード： 障害者

My ACE (Adverse Childhood Experience) score is 6. According to numerous academic studies, that puts me at risk for over 23 negative health outcomes, including diabetes, cardiovascular, digestive, respiratory and liver disease, cancer, and mental health issues such as anxiety, depression and thoughts of suicide.

“Honey, you’ve been very ill and they’ve had to amputate…” His voice cracked. I searched his face, looking for some kind of clue to tell me why I sensed so much pain from him and in me. “…Your hands and feet.” Cyndi tried to grasp the new reality that flesh-eating disease had changed her life forever. Her recent memories of being a successful business manager and new mom seemed oceans away. It just couldn’t be true. I tried to speak, but no words came. Please God—let this be a dream.

Aos 22 anos, um acontecimento inesperado tornou Andrea Schwarz em uma pessoa com deficiência, desafiando seus sonhos e projetos para o futuro. Enfrentando as barreiras impostas pela sociedade, a autora transformou seus desafios em asas. Com coragem, disciplina e uma pitada de rebeldia, ela enfrentou as dificuldades e demonstrou que é possível construir uma vida admirável e alcançar realizações significativas.

I finished my first book, Multiple Sclerosis: A Blessing in Disguise, around the end of 1998. At that time, I was going through a lot of issues that I thought were very important to me. That book told of my discovery, my eventual acceptance of the illness, and how I dealt with what was happening to me. Like anybody else who is faced with the burden of discovery, I had a lot of questions that I felt I really needed to answer, but I never sought to answer why this had happened to me.

Written by Mark Holt-Rogers, a Wellbeing Specialist with over a decade of experience living with Parkinson’s, Shaken is one of the most insightful and practical Parkinson's audiobooks available today. Designed for patients, families, friends, and caregivers, this essential guide draws from Mark’s personal experiences and expertise to provide actionable strategies and emotional support for managing Parkinson’s disease.

"If you can dream it, you can do it!" - das ist bei Oliver Brünner keine Floskel. Dabei sah im Leben des heute erfolgreichen Speakers eigentlich alles ganz anders aus. Noch während seiner Geburt zieht sich die Nabelschnur seiner Mutter wie eine Schlinge um seinen Hals, weswegen er fortan mit einer spastischen Tetraparese lebt. Doch Oliver trotzt den vermeintlichen Widrigkeiten und kann heute auf einen Lebensweg zurückblicken, den dem schon früh als "Sorgenkind" titulierten Jungen wohl niemand zugetraut hätte. Seine Geheimwaffe: das Träumen.

Kathleen O’Neill courageously chronicles her journey through the turbulent realms of bipolar disorder, addiction, and recovery. With raw honesty and resilience, Kathleen shares the battles she fought within herself and against social stigmas, laying bare her struggles, triumphs, and the moments of grace that shaped her healing. This memoir offers a compelling look at the complex layers of mental health , the strength of the human spirit, and the transformative power of hope.

Life with Louie is a collection of coming-of-age stories about growing up with a brother who happens to have been born with Down syndrome. For the author, Mia Rotella-White, having a sibling with a disability never created hardship. The opposite is true. Growing up with Louie meant Mia’s days were full of disco balls, group hugs, fashion shows and dance parties. When adversity struck, and it did, the siblings reminded each other how ridiculous it was to think any tragedy could ever be bigger than their love.

An upcoming book to be published by Penguin Random House.

Wayne Magee is on a mission to empower those who have been repeatedly told, “You can’t!” He has spent his life overcoming obstacles and negative labels intended to convince him that he could not lead a purposeful, fulfilled life. At birth, he was diagnosed with cleidocranial dysplasia, which is a rare genetic skeletal disorder that affects one in one million people. Countless medical professionals stated that he would not live beyond two years old. Wayne’s story demonstrates that for every tough blow, we have an innate ability to overcome societal and medical challenges.

Rachael Kurgan is a young woman who has already experienced a lifetime's worth of trials and tribulations. From grappling with a disability from birth to the heartbreaking loss of both parents, she has already absorbed some of the most difficult blows that life can throw at a person. But through her faith in God, perseverance, and the support of friends and family, she has not only overcome all of these difficulties, but established a happy and thriving life.

Based on a true story, Stern by Name, Stern by Nature offers an unflinching and intimate portrayal of one of the UK's most promising and eminent philosophers. This groundbreaking work delves deep into the psyche of the protagonist as he navigates the tumultuous landscape of mental health struggles.

While studying as a biology undergrad at UC Santa Cruz, Ian Mackay crashed his bike into a tree on campus. Paralyzed from the shoulders down, Mackay adapted to his new life with the help of his dedicated family, particularly his mother, Teena Woodward, and a group of quirky friends. After years of despair, and against all odds, he became an inspiring leader, an innovator with Apple, and a world-record-breaking athlete.

At the age of forty-three, Amy Lee Lillard learned she was autistic. She learned she was part of a community of unseen women who fell through the gaps due to medical bias and social stereotypes. A Grotesque Animal explores the making, unmaking, and making again of a woman with an undiagnosed disorder. How did a working-­class background and a deep-rooted Midwest culture of silence lead to hiding in plain sight for decades? How did sexuality and anger hide the roots of trauma among the women in her family?

Inside this moving true story, John Furniss, more famously known today as "The Blind Woodsman," along with his wife, inspiration, and fellow artist Anni share their amazing story with the mission to help and inspire others to pursue their own creative passions, regardless of the challenges they may face. The Blind Woodsman is a compelling true story that will give hope and inspiration to those dealing with disabilities, mental health struggles, addiction, chronic illness, and the anxieties and stresses in our everyday lives.

Embark on a powerful and inspirational journey with Dawn Green as she battles against the odds in a 35-year-long quest to uncover the truth behind her mysterious and life-threatening health issues. This gripping memoir takes listeners through the highs and lows of an extraordinary life marked by persistence, resilience, and unwavering hope. The book opens with the author's early years, when she first realized that her health was beginning to decline. In succession, a series of perplexing symptoms began to plague her.

Raymond Antrobus was first diagnosed as deaf at the age of six. He discovered he had missing sounds—bird calls, whistles, kettles, alarms. Teachers thought he was slow and disruptive, some didn’t believe he was deaf at all. The Quiet Ear tells the story of Antrobus’s upbringing at the intersection of race and disability. Growing up in East London to an English mother and Jamaican father, educated in both mainstream and deaf schooling systems, Antrobus explores the shame of miscommunication, the joy of finding community, and shines a light on deaf education.

Taking us through a criminalised underworld of pubs, parties and campaign gatherings, The Light of Day charts how Roger Butler helped bring about a change in the law, legalising sex between men, but soon found himself marginalised from the movement he kickstarted after becoming completely blind in his early 30s. Worn down trying to navigate life afresh in London, he left for Oxford, where he became increasingly isolated and never found the life partner he so desperately wanted.

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.

Obsessed with music as a child - listening to everything he could lay his hands on, going to gigs, starting a band, and then pursuing a career in music journalism - John Harris had no idea that he was in fact preparing himself for the greatest challenge of his life. But so it transpired. When his son James was born, and three years later diagnosed with autism, music became their main form of communication, a hugely shared passion and - it is no exaggeration to say - the sound that saved them. John Harris tells the story of how music has opened up the world to James, one song at a time.