Showing results by publisher "----RM Alexander" in People with Disabilities

Imagine a simple thing like a round stone underfoot or an unnoticed overhead danger, and how quickly life can take a dramatic turn. For Iain MacLeod, it was a slippery mattress cover. Iain MacLeod's memoir draws us into the experience of those who live with a physical disability, and it speaks to the challenges they must overcome on a daily basis. “Billions of people get out of bed every day without any problem, but when I got out of bed that day, it went horribly wrong,” says MacLeod, a Scotsman with Cerebral Palsy.

Randy Pierce was 22 years old, fresh out of college, and thriving at an excellent job. His promising future seemed certain. Then, in just two short and devastating weeks, an unexpected neurological disorder plunged him into blindness. Randy, believing his future had vanished in the blink of an eye, wondered, “How can my life have meaning now?” Before he could fully answer, he had further to fall. Blindness was far from the worst challenge he would face. See You at the Summit is Randy’s uplifting personal account of his journey through adversity to accomplishment.

Marilyn Elaine Lundberg’s true crime memoir, Jagger’s Eyes, is a brutally honest account of how one unfortunate little girl turned to animals for love, safety, and comfort. The trauma of incest and neglect occurred behind closed doors in her Christian home and crippled her psychologically as a child. Her attacks produced PTSD, suicidal depression, chronic anxiety, panic attacks, agoraphobia, anorexia, plus more, and she was housebound for many years as an adult.

By the time native Sicilian Mariagrazia Buttitta turned 26, she’d planned out the perfect life. After finishing her residency in Buongiorno Medical School, she’d be primed for a job at the prestigious Roma Hospital, the first step toward becoming an Italian Dr. Oz. Instead, she wakes up to discover a medical diagnosis that leaves her almost completely blind. Her family, frustrated and desperate, seeks medical aid in the US, but it comes with a steep price.

I am a woman living with cerebral palsy (CP) since birth. When I was prepping for graduation and finishing my final honors essay for school, I had a realization that based on experience, most of the world does not think or experience life the way I do. Despite my CP, the world still didn't seem to process experiences, feelings, or ideas the same way I've learned to be my normal way of functioning.

At 35, the same age as his mother when she had her accident, Mitch began experiencing symptoms of primary progressive multiple sclerosis, a particularly disabling form of MS, and his physical challenges grew to resemble his mother’s. In the ensuing years, he muddled through the ethical swampland of clinical trials, navigated the minefield of experimental treatments, and became a popular blogger and disability advocate. Equal parts entertaining and inspiring, Enjoying the Ride tells an extraordinary mother and son story.

At the age of 16, Marc Hoberman moved from Yonkers, New York, to Hollywood, Florida. Moving away from his friends was hard enough, but being diagnosed with epilepsy shortly thereafter was even harder. Marc’s story follows him from high school up to his present-day life as an author, teacher, husband, and father. His struggles with seizures, toxic medications, and loneliness were a certain recipe for disaster. Marc’s sense of humor, support network, and successful search for a doctor who would save his life prompted him to make his private story public.

At birth, few people knew if Scotty Crabtree would live past infancy. Growing up with cerebral palsy, his future was uncertain. Thanks to the company of family and friends in the Bakersfield community, he would be “just fine”. Despite losing loved ones, undergoing painful surgery, and life’s daily obstacles, Scotty believes in celebrating life and pursuing his dreams as a country music artist - especially since the fateful night one man told him one thing: “You can do anything you set your mind to....”

Life moves fast. Too fast for some people. This is the true story of what it's like to live in a world where you can't keep up. Bobby was ten months old when my mom and dad rescued him from birth parents who were slowly killing him. He was adopted into our family after a lengthy custody battle. Instead of that settling him, it set off a lifelong struggle to find a place to belong, a place to call home. Like an old-fashioned merry-go-round, the world moved at a speed that was just too fast for Bobby. He couldn't keep up, which prevented him from keeping a job.

Theresa Marafito, daughter of Irish immigrant parents, was born in 1933 in New York City, blind in one eye with partial vision in the other. She was a precocious child who wanted to appear “normal” to her peers and family, regardless of her disability. Her game was to be independent, not dependent, and would rarely ask for help. At 19, she graduated magna cum laude with two master’s degrees. Theresa and her husband, Jerry, who was also visually impaired, would build a house on a shoestring budget and had two daughters; one who was also born visually impaired.

I moved to Alaska with less than two weeks' notice to save my grandparent's lives. With Parkinson's disease, diabetes, heart failure, high cholesterol, blood clots, and more to contend with, I have quite the task at hand. I will use holistic healing modalities to prolong and improve the quality of my family's life, all while living on the Kenai Peninsula of Alaska. Ultimately I realized while writing this book that love is the answer to all of life's questions. Love can cure all.

Caleb Hudson had always taken things like breathing on his own, feeding himself, and walking as guarantees, but sometimes life changes in the blink of an eye. Faced with the uncertainties of paralysis, Caleb, as well as his parents and sister, must find a new way to not only survive but thrive.

I will state that though listed as a memoir, this is for the most part a fiction book subject (epilepsy Zen). They say that Yin Zen questioning is talking to your higher consciousness; epilepsy Zen meditation is contemplating your navel or lower than your tanzen - doorway to the hara and hearing the giant ocean roar from within a fragile seashell and learning the Yang illuminating answer.

The author describes in detail all the insanity, disturbing behaviors, oppressive symptoms, and various feeling associated with the mental battles within her own mind. The author suffers from clinical depression, bipolar disorder, schizophrenia, schizoaffective disorder, and borderline personality disorder. She struggles with suicidal thoughts and attempts, self-mutilating behaviors, mania, paranoia, anxiety, and psychosis with intense hallucinations of all five of her senses, and multiple delusions, including the belief that she is the "second-coming of Christ".

Le 3 avril 2015, on diagnostique à Marine, jeune étudiante dynamique de 21 ans, une sclérose en plaques, appelée plus communément SEP. L'urgence de la situation, le besoin de prendre une décision quant à la prise d'un traitement ou non et le manque d'informations, l'amène à s'interroger. "La maladie c'est toi qui l'as, il faut donc chercher la solution en toi." Son traitement ? Réaliser un projet rêvé : le voyage.

Mit 15 Jahren verliert der Deutsch-Singhalese Saliya Kahawatte innerhalb von Monaten einen Großteil seines Augenlichts. Die Ärzte sagen, dass er eines Tages völlig blind sein wird. Er soll die Schule verlassen und in die Blindenwerkstatt, er aber träumt von Abitur, Studium und selbstbestimmtem Leben. 15 Jahre lang verschweigt er seine Behinderung, um in der Welt der Sehenden Karriere machen zu können. Fingerspitzen, Ohren und seine Intuition ersetzen seine Augen.

She's never taught a class in her life. But when the City of Chicago calls on blind writer Beth Finke to teach a memoir-writing class for older adults, she reluctantly agrees. What she learns about her students, their stories, and herself will move and inspire you. Written the way Beth hears life, you will come to know and love Minerva, Wanda, Hannelore, and the whole colorful cast of characters who build a community around Beth's classes. Generously sprinkled with excerpts in her students' own voices, Beth's book will convince you to get your own stories down on paper.

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.

"Je vis avec l'autisme", écrit Josef Schovanec, soulignant ainsi ce qu'il considère plus comme une qualité que comme un handicap. Ce voyageur passionné des civilisations anciennes maîtrise une dizaine de langues, est diplômé de Sciences Po et possède un doctorat en philosophie. Il récuse pourtant les attributs qu'on lui prête - ceux d'un autiste "génial" aux capacités intellectuelles extraordinaires - pour évoquer plutôt, avec beaucoup d'humour et de sensibilité, ces "petits" problèmes qui font le quotidien d'un autiste Asperger.

In the context of bulling, we tend to focus on the don'ts. Don't point. Don't stare. Don't use hurtful words. Being the eternal optimist that he is, Joe challenges us to redirect our energy. Instead of not acting like a bully, he calls us to imitate the compassion of a friend. Subtle yet powerful, the examples Joe gives of people going out of their way to treat him like they would anyone else call all of us to action.