Showing titles in People with Disabilities

Driving Myasthenia Gravis Into Remission is a book based on the personal beliefs and experiences of the author Romerol Stanton regarding the autoimmune neurological disorder Myasthenia Gravis. It is a book that provides information on all-natural and alternative treatments that have been effective in alleviating the symptoms of Myasthenia Gravis. This book also gives insight into the author's trials, tribulations and triumphs living with Myasthenia Gravis.

Sara invites us to join her on a far more personal journey, this time, as she tests her own beliefs in the alternative health-care practices she’s learnt of over recent years. Presented with the urgency of “More tests needed right now!” when initial images reveal a lump measuring 4.5 centimetres by 1.2 centimetres in her left breast, she decides to follow a non-standard course or action.

When Ellie Goldstein was first diagnosed with Down Syndrome, her mother was soon told that her new-born would amount to nothing. For 21 years and counting, Ellie Goldstein has been defying the odds and overcoming every hardship thrown at her. Told she wouldn't walk, Ellie has danced on mainstages. Told she wouldn't learn, she has gained a college education. And told not to dream, Ellie has gone on to become the first model with Down Syndrome to be photographed for Gucci and continues to change the face of fashion from the inside out in countless international campaigns.

How Being a Nomad Saved My Life is the true story of Debra Dickinson and her journey through navigating a grim traumatic brain injury diagnosis, where she was told she wouldn’t make it to 2016, to thriving and living life on her own terms while being on the road as a full-time nomad. She gives you glimpses into her life: the ups and downs, the hardships and scary moments on the path she has taken to live authentically in every way possible while on the road. As you listen to her experiences, you’ll be inspired to find your own truth and to never give up, no matter what.

Like many of us, James Lindsay is no stranger to stress and anxiety. But in his case, leaving those struggles untreated led to a full psychotic episode that hospitalized him for the better part of a month. With the help of medication and therapy, he has now overcome this dark period and is currently living a much happier life.

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.

Meet Lionel, Caroline’s older brother. Born in the 1950s, when little was known about autism, Lionel was considered a peculiarity. From the beginning, he was a silent child, oblivious to the people around him and intent only on playing with his toy trucks. By the time he turned four, doctors declared him ineducable and advised that he be institutionalised – a shockingly standard practise at the time. Looking After is both a portrait of one autistic man's remarkable life, and a heart-rending story of how one family learnt to care for each other.

All I ever wanted was to be normal. But when I was diagnosed with a horrible disease, my life became filled with insurmountable challenges far from normal. Terrified I wouldn’t have a life worth living, I went to an academy where everything changed for me. I was exhilarated to discover my life was just beginning. Living without my parents and dealing with my disease alone scared me. But after making friends, my temporary home was better than I could have imagined

Author Eiren Caffall is the inheritor of a family legacy of two hundred years of genetic kidney disease and the mother of a child who may inherit that legacy. A literary memoir on loss, chronic illness, and generational healing, Caffall’s The Mourner’s Bestiary is also a meditation on grief and survival told through the stories of animals in two collapsing marine ecosystems—the Gulf of Maine and the Long Island Sound—and the lives of a family facing a life-threatening illness on their shores.

Schon als Teenager wusste Fern Brady, dass sie anders war. Als sie zufällig über Autismus las, wusste sie instinktiv, warum. Hier war die Erklärung für ihre Wahrnehmungsstörungen, ihre Meltdowns, ihre Unfähigkeit, soziale Signale zu deuten. Doch erst mit 34 folgte endlich die befreiende Diagnose. In dieser schonungslos ehrlichen Autobiografie erzählt sie ohne Rücksicht und mit dem ihr eigenen Witz von Neurodiversität zwischen Sexismus und Ableismus und ihrem offenen Umgang damit.

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.

Nadeem's journey is a story told by a mother about her son—it’s not just about a mothers love, it also shows his compassion towards her, his siblings, family and friends. It shows us how he never let his illness define who he was even when the doctors were curt and less kind with their delivery of information. This book tells us the story about a fight to survive, a story about a mother’s love for a child and a story about how a community comes together to support each other.

During an ordinary Fall afternoon, Kimber Hanchey-Ogden was delivered devastating news: Seth, her 17-year-old son, had been hit by a car and airlifted to a hospital! Having sustained a traumatic brain injury, doctors told her that if Seth made it, he would never be able to walk or talk; he would not remember his past or understand humor. And that was just for starters.

Have you ever felt like there was no light at the end of the tunnel? Or do you struggle why bad things are always happening to you? Do you feel like no one hears you and no one knows the pain and suffering inside of you? Then begin to search for a real understanding of your life and how important you are.

My name is Tzemah Yoreh, and I am a congregational rabbi on the autism spectrum. How is that possible? How can I thrive in a profession that is pastoral, that rewards extroversion, that seems mostly for those who intuitively grasp social dynamics? In So Compassionate it Hurts: My Life as a Rabbi on the Spectrum, I share my personal journey of being a religious leader on the spectrum, how I've used my gifts to positively impact my congregation (and, in turn, myself), and stories that I hope can inspire those with similar challenges to keep pushing and pursue their passions.

Annie and Rolf Lulloff were entering an exciting stage of life in 1976 when the first signs of health issues that lie ahead for Annie began to emerge. A sudden loss of sense of smell, severe anxiety attacks, vision issues, and other neurological challenges piled up, eventually culminating in a diagnosis of Parkinson’s disease on New Year’s Eve, 1989. But the Lulloffs were not about to let Parkinson’s get the best of them.

Musical director and arranger David Loud, a legendary Broadway talent, recounts his wildly entertaining and deeply poignant trek through the wilderness of his childhood and the edge-of-your-seat drama of a career on, in, under, and around Broadway for decades. He reveals his struggle against the ravages of Parkinson's and triumphs repeatedly. This memoir is also a remarkable love letter to music. Loud is the Ted Lasso of the theater business, ever the optimist!

“I never wanted to be hearing. I said this out loud in my TED talk, and the audience went bug-eyed, struggling to process this heresy. How could anyone not want to be hearing? I wasn’t anti-hearing. I just felt my life would be simpler if everyone else were deaf.” So begins the compelling story of acclaimed TED speaker Rebecca Knill as she guides us through a life shaped by hearing loss. Throughout, Knill offers eye-opening insights into disability and celebrates the power of technology to level the playing field.

Often used as a shorthand for tidiness or as the punchline of a joke, OCD is one of society’s most misunderstood disorders and it’s rarely spoken about with such honesty and openness. Beautifully written, moving and often darkly funny, Tuppence recounts what it feels like to share your mind with a nest of scorpions.

Uncommon Vision by Matt Hendrick is a deeply moving memoir that captures the essence of human resilience. After a devastating accident leaves him paralyzed, Matt embarks on a life-changing journey that challenges both his physical limits and his perceptions of the world. From the depths of despair in a hospital bed to his adventures in the digital and supernatural realms, Matt's story is a riveting exploration of recovery, self-discovery, and the relentless pursuit of one's dreams despite the odds.