Títulos em Pessoas com Deficiências

David Tatel has served nearly 30 years on America’s second highest court, the United States Court of Appeals for the D.C. Circuit, where many of our most crucial cases are resolved—or teed up for the Supreme Court. He has championed equal justice for his entire adult life; decided landmark environmental and voting cases; and embodied the ideal of what a great judge should be. Yet he has been blind for the past 50 of his 80-plus years.

Born four weeks premature and weighing little more than five pounds, Scott A. McCreight had a rough start and uncertain future. He was placed for adoption, but the good news didn’t last long: shortly after, Scott was diagnosed with cerebral palsy. Developmental delays permeated his childhood, the odds for a “normal” life seemingly stacked against him.

An inspiring and unforgettable memoir that provides hope to others who are experiencing depression, mania, or psychosis, RESILIENT is a deeply personal account about life with mental illness, hearing loss and resiliency. Liz's journey provides encouragement for patients, families, friends, and healthcare workers by showing that recovery is possible.

Arriving in the UK from Jamaica at the tender age of 14, Keisha shares her empowering lived experiences growing up with undiagnosed Dyslexia and Dyspraxia, while facing several intersectional challenges that include culture, race, and the UK education system.

See how, throughout her life, she became a believer, and even with Kerry and Kaylynn's love and support, she had to find the strength elsewhere to get up each and every day to be the best mom she could be for Austin. Listen to how still, to this day, she struggles with negative emotions and guilt and needs to be reminded often that God is in control, and he will never forsake her, even when she feels she is alone.

My life has been nothing short of a miracle. A true triumph, even in the midst of adversity. In Deaf Blind Champion, I give you a front-row seat into how my life changed when I heard my diagnosis, and what I did to get through the depression that engulfed me to become an accomplished sportsman, a dad, life partner, son, brother, teammate, and activist.

From our family to yours, here are humorous stories from our crazy past, mixed with ideas for handling some of the issues facing a family raising kids with autism. Inside you will find ideas for stimming aids, dietary help, and even links to companies who hire adults with autism. Humor, hope, and help for families like yours traveling Through the Wormhole.

«Sono Rachele e ho 29 anni. A un mese dalla nascita, è stato detto ai miei genitori che avevo la fibrosi cistica, una malattia genetica degenerativa da cui non si può guarire. La malattia non si vede perché colpisce principalmente gli organi interni; tutte le secrezioni sono alterate e molto dense, il muco ristagna ed è difficile respirare. Quando sono stata invitata a un evento della Fondazione per la Ricerca sulla Fibrosi Cistica, mi sono chiesta: come faccio a unire la mia passione per i motori con quello che mi sta più a cuore?»

Discover how a woman wheelchair user with cerebral palsy found purpose in librarianship and in ordained Christian ministry. Glean hints on how to live with purpose as a person with a physical disability. Gain clues on practical everyday living with a physical disability. Gather insights as friends and health professionals on how to relate to people with a physical disability. Appreciate how Christian faith can inform and strengthen motivation in the experience of physical disability.

À travers cet ouvrage, c'est un véritable message de courage et de persévérance que nous délivre Vincent. Mais plus encore, il nous offre son inspirante philosophie de vie et nous incite à ne jamais abandonner nos rêves et à aller au bout de nos passions. Vincent Vinel a sans conteste été la révélation de la soirée d'ouverture de la saison six de "The Voice". Devant plus de 6,8 millions de téléspectateurs, ce jeune chanteur malvoyant a d'emblée conquis les coaches.

Robert was a young man struggling to make it on his own when in 1990, he suffered a violent and traumatic experience when someone put a bullet through his brain. Robert tells the amazing story of survival during a time when life shriveled to dark emptiness and his future seemed hopeless.

When I found out I had cancer, I only knew one person who had beat it, and she did not come to mind. Finding out the president had beat it without chemo or radiation gave me hope. I feel my assistance was critical to my beating cancer. Your own research and knowledge, along with your gut feelings, will help guide you. This book is my belief, and I feel cancer is beatable because I was able to beat it. I believe thinking out of the box is sometimes the solution.

A story about a dead man walking. A journey through depression, happiness, divorce, death, survival, and so much more. Stories about life as a chef and life with a traumatic brain injury (TBI). These are the real stories about the difficult process of recovery from a motorcycle accident and how life continues afterward.

Growing up in Mineral Wells, Texas during the 1950s and 60s was anything but idyllic for Walter Ashby. Due to a misdiagnosis and medical error, his sister Janie went from being a lively young girl to a shell of a person who required their parents’ attention 24 hours a day, every day. To add insult to injury, his parents received another blow: before Walter was six-years-old, he lost 98 percent of his vision, leaving him legally blind.

This audiobook provides insight into the life of a neurodiverse Black girl from the Midlands as she embarks on her journey through the UK school system. This book unveils and highlights the unique experiences of neurodiverse people of color and the many challenges they face. In this book, 24-year-old British-Nigerian Oluseyitan Ojedokun gives an account of her struggles through school. She shares the many dreams and goals she had, despite the feeling of constant dismay.

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.

From being a little girl in a village in China with polio to a tech executive at Apple, Libo Cao Meyers has had quite a journey in life—a journey steeped in rich family legacy and powered by determination, growth, and love. Over the years and the miles, she’s embraced her differences and has allowed no one—including herself—to set limitations on what she’s able to accomplish. But just because she’s been successful doesn’t mean it’s been easy. Not by a long shot.

Sent blind soon after birth, David Hume stubbornly refused to live the limited life well-meaning elders and social norms expected. To date, that encompasses years in a blind institute, two marriages, grieving for two outstanding wives, founding recruiting firms, devising marketing techniques, facing business collapse, sailing ocean races, and through much of it, being the lead singer in popular bands. If you enjoy a short biography that inspires, saddens, cheers, and sticks in your memory, then don't put aside Blind Without Barriers.

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.

Andrea Lytle Peet was thirty-three years old—an urban planner living in D.C., newly married, and a triathlete—when she received the death sentence of an ALS diagnosis (also known as Lou Gehrig's disease). After grappling with the fact that she will likely become paralyzed and die within two to five years, Andrea experienced an unexpected spark that changes her outlook in the most magnificent way.