Títulos em Pessoas com Deficiências

Discover Linda Hoopes’ inspiring journey of resilience and triumph over macular degeneration in Co-Creating A Meaningful Life With Macular Degeneration. From fear to determination, her story will captivate your heart and empower you to embrace life’s challenges. Join her on this transformative path and find the strength to overcome obstacles, live fully and cherish every moment. Hoopes honestly shares the physical, emotional and spiritual transitions necessary to not only meet difficult challenges but how to thrive in spite of them.

From childhood stutterer to inspirational speaker! The Courage to Shine is a powerful and inspirational memoir by Eileen Forrestal, a former anesthesiologist who transformed her life. After a lifetime of "putting people to sleep", Eileen is now in the business of "waking people up" as a writer, speaker, and coach. In The Courage to Shine, Eileen retraces her journey. She shares her childhood trauma of an accidental overdose of junior aspirin that led to her subsequent speech impediment, the embarrassment of which caused her to hide her voice in silent shame.

In this inspiring memoir, Emily Falcon chronicles her lifelong journey with a congenital cardiac condition. In 1982, at seven weeks old, she had a heart attack that destroyed 40 percent of the left side of her heart. This was her entry into a world of multiple cardiac procedures, surgeries, hospitalizations, and a later diagnosis of glaucoma. Balancing these serious conditions defined her life.

A sudden rise in opioid addicts coinciding with a sudden drop in legally available opioids, created a desperation for prescription drugs never seen before in this country. Physicians shut down their previous practice of repeated refills, once the death toll was too high to ignore. As hospitals and rehab facilities instituted drug testing and CORI checks to ensure employees were clean, one health-care option stood alone as a place to easily obtain painkillers. That place was home health care.

This honest, outspoken and thought-provoking memoir by award-winning writer and appearance activist Carly Findlay will challenge all your assumptions and beliefs about what it is like to have a visibly different appearance. Carly lives with a rare skin condition, Ichthyosis, and what she faces every day, and what she has to live with, will have you cheering for her and her courage and irrepressible spirit. This is both a moving memoir and a proud manifesto on disability and appearance diversity issues.

Je m'appelle Mason Cyrille Elong Ewing. J'avais à peine 4 ans lorsque ma mère Marie est décédée, laissant derrière elle un petit bout d'homme. Au Cameroun, on m'appelait Toro, j'étais l'enfant au destin fragile. Puis je suis arrivé en France chez mon oncle et ma tante, pour une meilleure vie. On m'avait promis un fabuleux voyage, mais personne ne m'avait précisé que c'était pour l'enfer. J'étais devenu, Lucien, l'esclave.

As a 14-year-old psych ward patient, Harry realized he had a choice: let anorexia keep ruining his life or fight back against everything his mind told him was true. Now 22 years old, Harry delicately pieces together how his mind derailed to that point, what’s happened since he made his choice, and most importantly, what it’s taught him about life and how best to live it.

Why the Cane? is a personal memoir which recounts the true story of a man’s regaining a level of activity he thought would not be possible after a devastating injury. It chronicles his medical journey, the upheaval suffered by his family, and the counsel and support which shifted his focus and provided a framework to make thoughtful decisions for the long term.

Life is difficult for many people who face great dilemmas. For them, life can be a blur. However, this statement will be quite literal when you only put yourself in my shoes. For years now, I have suffered. During my teenage years, I was diagnosed with an untreatable nerve condition that tragically made me lose my sight within a speck of time. Since then, I had to learn and adapt to my new way of living—as a young blind adult.

In Turning Tragedy Into Triumph, Michael Bush fearlessly opens up about his extraordinary battle with both mental health challenges and the harrowing ordeal of fighting and surviving stage 4 cancer. Through gripping honesty and unwavering vulnerability, Bush takes listeners on an emotional rollercoaster, from the depths of despair to the pinnacle of triumph, demonstrating the indomitable human spirit's capacity for resilience and transformation.

As I watched my four darling children from my wheelchair, I realized this battle through illness had never been about ringing the bell and surviving the fire. I had what mattered all along. The only thing more powerful than fear, sickness, regret, and loss...the only thing stronger than death is love. Nothing could take that away from me.

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.

For many years, Jeffrey Demitrack searched for a meaningful and fulfilling relationship and, most of all, hoped that one day he would find a significant other who understood and unconditionally accepted his struggles with epilepsy. People have their insecurities, and relationships already are hard without throwing seizures into the mix, so his search has been a challenging one.

In this audiobook, you will catch intimate glimpses of how manic depression or bipolar disorder affects not only those diagnosed but the entire support structure around them. You'll find inspiration and hope that our fractured mental health system still holds opportunities for healing and unearthing resilience. In Hard Pill to Swallow: My Manic Memoir, Logan carries you through his struggles with his identity as a gay/bisexual man coming to terms with addiction while simultaneously battling bipolar disorder.

In this honest and open account of life with her PDA daughter, Sasha, Steph Curtis reveals the everyday struggles and explores the milestones of raising a child diagnosed with Pathological Demand Avoidance. This book guides you through the Curtis family's 'lightbulb moment' of recognising Sasha's PDA profile following her autism diagnosis at the age of two, their experiences of various education settings and attempts to access support, everyday life at home and relationships with family and friends.

Have you ever been around people, yet still felt alone? Dr. bird has too. Within the first variant of their envirusmental series, they revealed thirty years of their late-in-life realized secrets. In this second volume, they, literally and figuratively, Zoom in on the last four "unprecedented" ones. This includes them cutting-the-s--t about how, half-way through their PhD, COVID-19 hit. And how, a couple years later, they added "Dr." to the front of their nickname.

My journey with mental illness, specifically bipolar disorder, has woven itself throughout my life for 40 years. Whether it was active, or dormant, it has always lurked in the shadows. But, this illness, like any illness, can be managed and maintained.This story is particularly relevant for today's society. It is our charge to know a segment of our society who, for the most part, is misunderstood. When the Brakes Fail provides a forum for understanding the myths, the injustices, and the stigma of mental illness.

Doctors used to tell him he was cured. That was a long time ago. Ever since he first left home at age nineteen, writer Jason Jobin has had cancer. Every five years, like clockwork, it relapses, and yet he always pulls through, surrounded by friends and family but isolated by illness. Chemotherapy, surgeries, radiation—these persist, but they aren't the milestones of his life. They can't be, he won't let them be. From helicoptering into the Yukon backcountry to teaching in an elite writing program, Jason strives to enter adulthood with some normalcy, but his is the life of "a special case."

A revelatory collection of essays on the DeafBlind experience, and a manifesto on the power and untapped potential of touch. Born Deaf into an ASL-speaking family and blind by adolescence, John Lee Clark learned to embrace the possibilities of his tactile world. He is on the frontlines of the Protactile movement, which gave birth to an unprecedented tactile language and a way of life based on physical connection.

Andrea struggles to mourn a man who is still alive as she witnesses her father decline into the depths of Alzheimer's. Denial and devastation color her life when she learns her father, Richard, a recently retired surgeon, is diagnosed with Alzheimer's at the age of 67. Her dream to grow closer to him is crushed as the reality of his disease is fully realized. Andrea, a mother of three young children, learns to balance motherhood with daughterhood as she grapples to accept her father's fate.