Showing titles in People with Disabilities

DJ is the eldest daughter of four kids. Her Mom was born blind and raised her and her siblings. When DJ was 10 years old her mom’s health started to have complications. When her mom was in her 50s, she went through another health situation. She shares what it was like to start taking care of her mom. How does it work for a daughter to care for her mother?

As an adult, DJ has a son born with a congenital heart defect. She uses the things she learned while caring for her mother to care for her son. Learn how God has been the strong hold for this family through the many health trials they have gone through. This book asks the question: will you use what God is doing in your life for good?

En este libro de memorias profundamente conmovedor y sincero, Blanca Reyes Méndez comparte su viaje tras la pérdida repentina e irreversible de la visión de su ojo izquierdo. A través de la reflexión poética y la verdad personal, explora el dolor, el miedo, la curación y la transformación. Ver con el alma no trata sólo de la pérdida de visión, sino de aprender a ver de otra manera. A encontrar la luz interior. A vivir más despacio, más plenamente y con el corazón bien abierto.

Against All Odds is a story of an autistic child who, with courage and determination, struggles through life stages, achieving goals. It is a story of taking opportunities and never giving up. It is a story of the lessons learned to help every parent of an autistic child to see the possibilities instead of the challenges. Autism doesn’t have to limit your child’s potential.

Struggle. Overcome. Inspire. For Jacky Hunt-Broersma, a cancer diagnosis in her mid-twenties brought a life-changing challenge: a below-the-knee amputation. Navigating her new reality, Jacky first kept her difference hidden as she learned to walk and do daily activities using a prosthesis. Years...

Imbalanced traces Sheri Thomas' remarkable journey from a front-page headline in 1962 to her current role as an advocate fighting to remove the stigmas surrounding physical disabilities and mental health.

Part one of Three Years With A Monster comes to you in real time as Dennis scribbled it down in his journal and recapped the events every few months in blog form. You will experience the heartbreaking daily struggle as it unfolds. Eating disorders are nearly impossible to understand unless you come face-to-face with them. This book brings you so close you can smell the monster’s breath. The Wilkinsons were directed to use family-based therapy and dialectical behavioural therapy. Helpful explanations and observations of these tools are contained in this section.

Desde la infancia hasta la maternidad, Fernanda Gamboa comparte su experiencia vital con el Trastorno por Déficit de Atención e Hiperactividad (TDAH), revelando cómo una diferencia neurológica puede convertirse en fuente de fortaleza. A través de historias íntimas, anécdotas conmovedoras y reflexiones profundas, esta obra guía al lector por un viaje de autoconocimiento, sanación y empoderamiento. Con un enfoque práctico y humano, la autora desmitifica el diagnóstico, ofrece herramientas para familias y parejas, y construye una comunidad de aceptación: la Tribu Especial-Mente.

Helen Keller’s name is forever linked with courage, perseverance, and the power of education. In Midstream: My Later Life, she picks up where The Story of My Life left off, offering a rare look at her journey beyond her early triumphs. Here, Keller recounts the challenges and victories of adulthood—her advocacy for people with disabilities, her international travels, her friendships with world leaders and artists, and her tireless fight for social change. She writes candidly about setbacks, loneliness, and the weight of public life, but also about the deep sense of purpose that guided her.

Damiano e Margherita sono due fratelli che hanno molte cose in comune: la voglia di mettersi in gioco, la caparbietà e la tenacia nel voler inseguire i propri sogni, e l'autismo. Insieme si sono esibiti in televisione e, mano nella mano sul palcoscenico, sembrano finalmente aver trovato il loro posto nel mondo. Già dalla mattina successiva, però, i due sono obbligati a tornare alla realtà. Damiano vive a Rimini e ha le idee molto chiare sul futuro: una moglie – "l'altra metà della mela" – con cui avere dai dodici ai venti figli, milioni di dischi venduti, concerti in tutto il mondo.

How I Own Cerebral Palsy is a captivating look into the life of Carmen Lebron, a young woman set on living a life of positive impact free from physical and mental barriers. Heartfelt, honest, and full of liberating moments for the soul, Carmen's story is a riveting testament to why we should never, under any circumstances, consider giving up.

When she was 54, Lisa Knopp’s weight dropped to a number on the scale that she hadn’t seen since seventh grade. The severe food restricting that left her thin and sick when she was 15 and 25 had returned. This time, she was determined to understand the causes of her malady and how she could heal from a condition that is caused by a tangle of genetic, biological, familial, psychological, cultural, and spiritual factors.

In Rolling in Grace: Volume 1 – A Foundation of Faith and Imagination, author Brooke Brown shares her deeply inspiring life story — one defined not by limitation, but by extraordinary faith, resilience, and a radiant imagination. Narrated with warmth and authenticity by Kaylee Oro, this audiobook invites listeners into Brooke’s world, where hope triumphs over hardship and God’s grace lights every path.

This is the true story of a very special man whose life was suddenly and forever changed by a rare disease. Dealing with a severe backache for three days, he was taken to an emergency room. For five grueling months, his dignity, as well as his very self was stripped away. Trapped in a system that all too often is not healthcare, but Healthcareless.

Having gone from standing atop high mountain peaks to becoming a martial art and close-quarter combat specialist, and surviving 18 years of brutal special operations involvement, White Wolf's life took a turn that led him to face his most challenging adversary. His development of chronic illness sent his life tumbling headlong into an abyss where a maelstrom awaited. Invisible combatants threw his body into chaos.

Could you survive a month without the internet? Robert Kingett didn’t think he could—until a friend dared him to try. The catch? Robert is blind, and he relies on the internet for everything. For thirty days he must use no Google. No social media. No online banking, shopping or job hunting. Ultimately, no digital shortcuts to help him navigate a world that’s already built to ignore people with disabilities.

It was August 25, 2006, my first on-camera studio open for the CBS News broadcast 60 Minutes. Executive Producer Jeff Fager poked his head in the dressing room." Good luck, Brotha! You've come a long way to get here. You've earned it." …If only he knew. My mind flashed back to elementary...

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.

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.