Títulos em Pessoas com Deficiências

Condamné par la maladie, Olivier Goy partage avec la journaliste Anne Fulda son inlassable combat pour mieux faire accepter le handicap et lever des fonds pour la recherche, et, surtout, appelle à regarder et aimer la vie pleinement?! Olivier a 46 ans quand on lui diagnostique la maladie de Charcot en 2020. Une maladie neurodégénérative qui se traduit par une paralysie progressive des muscles, mais laisse au malade ses pleines capacités intellectuelles. Espérance de vie?: 3 à 5 ans.

A unique self-help memoir subliminally written from the perspective of a first time mom with undiagnosed Adhd, raised in Saint Louis, Missouri. She studied her experiences and those around her to recognize and identify, unhealthy patterns in society. Motherhood illuminated the struggles and weight that women have been thanklessly carrying for centuries. Producing emotionally unstable and traumatized children that become adults and spread their pain and grief among society.

Sometimes the best way to understand what’s deep inside requires looking outward. Sometimes the best way to understand the world outside requires a deep dive within. And sometimes, those two things are so intertwined it’s difficult to tell where one begins and the other ends. The Forest of My Youth is a collection of poems and perspectives that probe some of the deepest, most profound and sometimes achingly painful thoughts and questions I’ve had since my spinal cord injury in 1993.

"SpoonieNinja: Finding Strength in the Shadows" is an inspiring and intimate exploration of resilience and self-discovery in the face of chronic illness. Through raw and reflective storytelling, the book delves into the hidden battles, strength, and courage that come from living with a condition that often goes unseen. Tesla Coyle invites listeners to find empowerment in vulnerability and to embrace their own inner strength, even in the darkest of times. This book is a beacon for anyone seeking understanding, hope, and solidarity in their own journey through life's challenges.

This memoir combines the drastic losses which occur due to severe episodic memory deficits with the greater agency currently afforded to all of us as made capable via ingenuity and technology. In this book memory loss is considered within the present-day environment of novel solutions heretofore unimaginable. All of us may never need to worry about recalling key life events ever again.

Rachel Kolb was born profoundly deaf the same year that the Americans with Disabilities Act (ADA) was passed, and she grew up as part of the first generation of deaf people with legal rights to accessibility services. Still, from a young age, she contorted herself to expectations set by a world that prioritizes hearing people. Now in Articulate, Kolb blends personal narrative with cultural commentary to explore the different layers of deafness, language, and voice.

Dr. Paul Boskind, a successful psychologist and LGBTQ+ advocate, thought he had everything under control. Diagnosed with a blinding retinal disorder at twenty-one, he defied the odds, building a fulfilling life. But years earlier than expected, his vision began to fade. The Blind Man Game is Paul’s poignant journey of self-discovery as he navigates the emotional turmoil of losing his sight and sense of self. With his future uncertain, Paul must draw on his expertise and inner strength to confront grief, fear, and a world no longer designed for him.

You have big dreams… Yet it seems there’s always something standing in your way, and reaching them feels impossible. It’s overwhelming, and it’s far less scary to hit the snooze button, roll back over, and carry on living life as you know it… But your fear is what’s really holding you back… and you can overcome it. Every setback you face is an opportunity in disguise, and you can push past every limit that stands in the way of your dreams.

Barbara Anderson narrates with brutal honesty the day-to-day experience of having a child with disabilities: the challenges inside and outside the home, health and life complications, the shifting priorities, the daily Mt. Everest-sized struggle of having a child with an—until now—irreversible diagnosis such as infantile cerebral palsy.

The forms of intimacy and care that we’ve been sold are woefully inadequate and problematic. In a world that treats those who are sick and traumatized as problems in need of a cure, nonbinary writer, artist, educator, and Instagram creator Margeaux Feldman offers a different story. Trauma, which all too often manifests as chronic illness, tells us that there is something deeply wrong with the world we live in. A world that promotes individualism, fractures us from community through violence and systemic oppression, and leaves us traumatized. That is what we need to cure.

Escaping the Vulture's Shadow is a deeply personal and eye-opening memoir by Spencer Stern, chronicling his two-decade-long battle with the psychiatric system. Stern's journey began with an unexpected mental health diagnosis in his early twenties, leading to years of interventions, psychotropic medications, and repeated hospitalisations. In a candid and reflective narrative, Stern exposes the harsh realities of modern psychiatric practices, questioning their effectiveness and ethical foundations.

BUT...GOD Gave Me a Pencil is an autobiographical memoir in which Dr. Rhonda Richmond explores her transformative journey from being abandoned by her mother to accepting her autism and learning disabilities in reading, writing, and math. Despite being functionally illiterate when she graduated high school, Dr. Richmond developed a pathway to literacy and began teaching her own children to read and write. Working with her children supported her creation of a new way to teach literacy skills, which helped her as a special education teacher and principal.

Embark on a powerful and inspirational journey with Dawn Green as she battles against the odds in a 35-year-long quest to uncover the truth behind her mysterious and life-threatening health issues. This gripping memoir takes listeners through the highs and lows of an extraordinary life marked by persistence, resilience, and unwavering hope. The book opens with the author's early years, when she first realized that her health was beginning to decline. In succession, a series of perplexing symptoms began to plague 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 Antrobus’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, Antrobus explores the shame of miscommunication, the joy of finding community, and shines a light on deaf education.

Taking us through a criminalised underworld of pubs, parties and campaign gatherings, The Light of Day charts how Roger Butler helped bring about a change in the law, legalising sex between men, but soon found himself marginalised from the movement he kickstarted after becoming completely blind in his early 30s. Worn down trying to navigate life afresh in London, he left for Oxford, where he became increasingly isolated and never found the life partner he so desperately wanted.

In "You're Not Doing It Right," Ellen Patnaude bravely opens the door to the haunting reality of Lewy body dementia (LBD) and unravels its profound impact on families. One of the most common types of dementia after Alzheimer's disease, LBD is marked by fluctuations in cognition, hallucinations, and motor symptoms. The journey begins with subtle warnings of small changes in her mother's behavior that worry Patnaude's father, but go unnoticed by the author and her sibling.

Obsessed with music as a child - listening to everything he could lay his hands on, going to gigs, starting a band, and then pursuing a career in music journalism - John Harris had no idea that he was in fact preparing himself for the greatest challenge of his life. But so it transpired. When his son James was born, and three years later diagnosed with autism, music became their main form of communication, a hugely shared passion and - it is no exaggeration to say - the sound that saved them. John Harris tells the story of how music has opened up the world to James, one song at a time.

Inspired by a journal she kept between the ages of 14 and 26, Ann Melim shares a moving and honest portrayal of her harrowing journey with undiagnosed bipolar disorder. She captivates the listeners with stories of psychotic breaks triggered by dead birds, an impulsive elopement and rooming with a schizophrenic horse whisperer.

The story of one man’s experience of a major stroke and his attempts to recover from it ….. but, enough of that - this is also an account of a dog’s experience of life with unpredictable, irrational human beings and his attempts to deal with all of that.

Stroke of Love is the life story of a young stroke survivor from Texas named Hether Flanigan. It is a story of resilience, determination, strength, and love. A story about the human spirit, the will to live life to the fullest, the power of the human mind, and the love that surrounds us.