Títulos em Pessoas com Deficiências

Living with multiple sclerosis was never going to be easy. The phrase 'I rule it, it doesn't rule me' was to become Lydia's benchmark. She clung fiercely to these words. They would booster her strength in the years ahead when at times, fear of the pain and its affects, especially the horrendous agony of an MS attack, would almost break her.

Raymond Antrobus was first diagnosed as deaf at the age of six. He discovered he had missing sounds—bird calls, whistles, kettles, alarms. Teachers thought he was slow and disruptive, some didn't believe he was deaf at all. The Quiet Ear tells the story of Raymond's upbringing at the intersection of race and disability. Growing up in East London to an English mother and Jamaican father, educated in both mainstream and deaf schooling systems, Raymond explores the shame of miscommunication, the joy of finding community and shines a light on the decline of deaf education in Britain.

Beyond What You See is the eagerly awaited sequel to Confessions from Disability Limbo. Author Kevin Nuñez guides listeners through an active spiritual journey spanning from January 2022 to spring 2025, expanding from disability awareness to God awareness. Kevin uses a fun conversational style to lift others beyond their circumstances. After feeling lost for several years, Kevin realized there was more to his life than his physical limitations. His physical weaknesses revealed his strengths.

Learning to adapt to life after being diagnosed with chronic pain and illness is extremely difficult. Life as you knew it, along with your hopes and dreams for your life, literally gets turned upside down in an instant. This comes with a lot of deep complicated emotions from grief, sadness, anger, frustration to living in a constant state of uncertainty and stress. Most people assume that if you get sick, a medical professional like Dr. House will work endlessly until they have answers and a cure so you can go back to living the life you used to know.

Athena Stevens has never learned the name of the doctor whose lack of intervention at her birth lead to her cerebral palsy, but she feels the consequences of his actions – and inaction – every day. The factor observed first and foremost in her life will forever be the effects of what other people have done to her, rather than her accomplishments. And yet, she was groomed to believe that she would overcome any force that stood in her way.

Living with AuDHD is like being a unicorn—misunderstood, contradictory, and often invisible to others. You shine with creativity and innovation, but struggle to fit in — always feeling 'too much'. Autism and ADHD pull you in opposite directions, creating a lifetime of contradictions no one else can see. AuDHD isn’t listed in diagnostic manuals because until 2013, you couldn’t be diagnosed with both conditions — despite a co-occurrence rate of approximately 50-70%. These two neurotypes often clash, like opposing magnets in the brain. ADHD craves novelty; autism resists change.

Uma coletânea das melhores crônicas publicadas no projeto Histórias de cego, inicialmente um blog e depois um canal de youtube onde muito além de contar um pouco da sua vivência em uma sociedade tão visual, Marcos Lima nos mostra o mundo por seus olhos.

Mother of Courage is the inspiring true story of a young woman who loses both arms in a boating accident, yet valiantly finishes dental school, marries, raises two boys, teaches at an historically Black medical college, and becomes a nationally known advocate for people with disabilities. With grace, humor, faith, and a large dose of determination, Margaret Chanin transforms her tragic physical loss into a triumph of the human spirit—and shares her light with everyone she meets.

Ada d’Adamo est danseuse. Elle a passé sa vie à rechercher la grâce, la perfection du geste. Lorsqu’elle met au monde Daria, rien ne l’avait préparée à devenir la mère d’une enfant lourdement handicapée, qui jamais ne pourra voir ni marcher. Elle commence alors à écrire et penser cet amour hors du commun qui la lie à Daria, où tout est sans cesse à inventer. Mais une dizaine d’années plus tard, Ada découvre qu’elle-même est malade.

Monday, March 11, 2024, was remarkably uneventful—indeed, frankly dull—until around 5 p.m. that evening when Carl Davies collapsed in a heap. It was a day that would change his life forever. Stroke Me! Recounts the story of his recovery from a near-catastrophic brain haemorrhage. The author details, in often graphic detail, every step of his journey, from the stroke itself to the pain of physical and occupational therapy. He leaves no stone unturned as he describes the impact his illness has had on him and his family. Stroke Me!

A witty and honest account about Lorraine Ansell’s journey with chronic pain due to Hypermobile Ehlers Danlos Syndrome. This genetic life long condition cannot be cured, only managed. Lorraine talks about her life in constant pain and how that has created her personality and even clothes choices. Lorraine’s life is a continual compromise of activities and choices. This book explores her journey as well as the issues with tissues which she now realises were actually a thing and how much pain she has been in. Listen to how she comes to face up to pain and learns to accept and work with pain.

In Parkinson's & Recreation 2, Dennis shares ways in which he and his wife are traversing the progression of PD and is first and foremost a written legacy he is attempting to leave for his family. As a part of this attempt, Dennis has gone on a journey of uncovering his family roots. What would you feel if you discovered Viking kings in your lineage? What would you feel if you uncovered the mystery of how the Jernigan line was woven throughout the fabric of English nobility? What would such revelations mean for you and your family?

While society called his disability an obstacle and limitation, Neil argued that his "flourishing dystonia" allowed him to think, explore, and create art in a way most people cannot. True to his words, Neil embraced every opportunity to experience life to its fullest, from navigating the Alaskan wilderness in a wheelchair to commanding the spotlight on stage. In this deeply personal account, Neil invites listeners into his world as he remembers adventures and escapades, triumphs and disappointments.

Discover a path to healing and hope after a breast cancer diagnosis. Through relatable anecdotes, coping tricks, and personal reflection, author and two-time survivor, Carol Wyllie, offers invaluable insight, encouragement, and a few laughs for anyone going through cancer or any of life's challenges.

In The Maniac with No Knees, Tyler Kania takes listeners on a raw, unfiltered ride through his journey with undiagnosed Bipolar I Disorder. From rugby fields to the edge of the Grand Canyon, from building a cryptocurrency start-up to coaching a women’s rugby team to victory, Tyler’s manic adventures push every boundary. Along the way, he uncovers a major tech scandal, survives run-ins with the Boston Mafia, and even attempts the unthinkable—before landing in a mental hospital, where he finally begins to heal.

As autistic children grow into teenagers, you will experience new challenges, both as a parent and as a family. Supporting the leap into adulthood can seem daunting, but here Carrie Cariello takes you through her journey with her son Jack, shining a light on how to help your young person prepare for different life stages and grow in independence. Carrie's own experiences form the basis of her deeply empathetic advice—in this warm, astute and thoughtful book she offers a guiding and steadying hand so you can move through periods of change with increased confidence and calm.

A seventy-year history of disability is threaded throughout these essays and intertwined with writing that celebrates lesbian love, explores the slapstick moments of life, and shares the obstacles and triumphs of becoming a writer later in life.

This true love story follows Lars and Amanda, two twenty-somethings who fall deeply in love, with big plans for their future together, only to have the rug pulled out from beneath them when Lars is diagnosed with Acute Lymphoblastic Leukemia at age 24. They must learn to adapt to "medical life", putting their hopes and dreams on pause, navigating side effects and difficult emotions, and missing out on the beauty of every day moments that some may take for granted.

Written in first-person, from the emotional perspective, My Quiet Fight for Home emphasizes Johnnie's lifelong efforts to develop communication and career skills, as well as essential character traits, like honesty, courage, kindness, and loyalty.

Una vita perfetta in ogni minimo difetto. Una storia che ci insegna a guardare al di là dei pregiudizi, delle paure e delle. discriminazioni, per ricordarci come si arriva al cuore delle cose. Alessandra è una nutrizionista che ama viaggiare, Luca è un ingegnere. appassionato di cucina. Sono una coppia normale, che vive con serenità una. gravidanza perfetta, fino a pochi istanti dopo il parto, quando ai neogenitori viene. un sospetto: gli occhi a mandorla della piccola Luna vogliono forse dire qualcosa? La diagnosi arriva subito: Luna ha la sindrome di Down.