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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.

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.

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.

Meet Lionel, Caroline’s older brother. Born in the 1950s, when little was known about autism, Lionel was considered a peculiarity. From the beginning, he was a silent child, oblivious to the people around him and intent only on playing with his toy trucks. By the time he turned four, doctors declared him ineducable and advised that he be institutionalised – a shockingly standard practise at the time. Looking After is both a portrait of one autistic man's remarkable life, and a heart-rending story of how one family learnt to care for each other.

While studying as a biology undergrad at UC Santa Cruz, Ian Mackay crashed his bike into a tree on campus. Paralyzed from the shoulders down, Mackay adapted to his new life with the help of his dedicated family, particularly his mother, Teena Woodward, and a group of quirky friends. After years of despair, and against all odds, he became an inspiring leader, an innovator with Apple, and a world-record-breaking athlete.

At the age of forty-three, Amy Lee Lillard learned she was autistic. She learned she was part of a community of unseen women who fell through the gaps due to medical bias and social stereotypes. A Grotesque Animal explores the making, unmaking, and making again of a woman with an undiagnosed disorder. How did a working-­class background and a deep-rooted Midwest culture of silence lead to hiding in plain sight for decades? How did sexuality and anger hide the roots of trauma among the women in her family?

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.

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?

On a September night in Montreal in 1993, Curtis Pride got his first Major League hit, prompting a long, emotional standing ovation from the crowd of 45,757 fans. Profoundly deaf since birth, Pride couldn’t hear their thunderous applause. But as the cheers grew louder and more insistent, he realized he was feeling those vibrations within his chest—an undeniable acknowledgment of an extraordinary achievement.

“Hanley’s dyslexia makes this audio format especially significant, as it represents an accessible way for readers with learning disabilities, just like him, to comprehend and enjoy his story.”—Booklist This program is read by the author, comedian and severe dyslexic Phil Hanley, who...

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.

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.

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.

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.

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.

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.

By age 25, Tracie Bork is a rising scientist and half of a power couple who throws lavish faculty parties. But beneath the perfect surface lurks the chaos she’s tried to control since childhood—and alarming physical symptoms she’d rather dismiss. Each year, she works more fiendishly than the one before as the complications to her health compound and become more mysterious until finally, she hits a wall, body, mind, and soul. In a series of honest inquiries and reflections, Bork chronicles her journey as a patient, academic, former military brat, and woman in search of faith.