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They were part of the Baby Boomer vanguard, three boys thrown together in a 1950s Southern California subdivision looking like most other boys of that era. Under coonskin hats they ran free all summer long inventing their own games and endless challenges, fought imaginary Indians and pirates in a nearby orange grove, and on occasion battled a neighborhood bully or two. Their greatest enemy, however, was an infectious disease called polio – a paralyzing scourge that maimed and too-often killed little kids.

From the remarkable man whose life inspired the heartstopping film, ‘I Swear’, a book that offers extraordinary insight into what it’s like to live with a severe form of Tourette’s Syndrome: a fascinating, complex condition that’s more common than most of us think (1 in 100 schoolchildren have the condition), and yet is chronically misunderstood.

One fine April day, Mary Ann Kenny’s husband died suddenly while jogging near their family home. In the months that followed, Mary Ann – who had no history of mental illness – began suffering from depression, and then from a terrifying succession of physical and psychological symptoms, including the delusion that her young children had been harmed by her medications.

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.

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.

"Rediscovering the World: A Journey through Anosmia" explores the little-known condition of anosmia—the loss of the sense of smell. James Rondepierre takes listeners on an inspiring journey, weaving together personal stories and scientific insights to uncover the profound impact of this condition. Through heartfelt narratives, listeners will witness the challenges and triumphs of individuals living with anosmia, from the emotional adjustments to their resilience and creativity in redefining life without smell.

A survivor of Guillain Barre Syndrome, this is the walk that led me to Tik-Tok. This audiobook recounts the events that molded me into the man that lived in your phones. Encouraged by friends and family that I had a story worth telling, I became a self-proclaimed autoimmune advocate on social media, whose ramblings captured the attention of fellow autoimmune, chronic illness, and chronic pain sufferers along the way.

My ACE (Adverse Childhood Experience) score is 6. According to numerous academic studies, that puts me at risk for over 23 negative health outcomes, including diabetes, cardiovascular, digestive, respiratory and liver disease, cancer, and mental health issues such as anxiety, depression and thoughts of suicide.

“Honey, you’ve been very ill and they’ve had to amputate…” His voice cracked. I searched his face, looking for some kind of clue to tell me why I sensed so much pain from him and in me. “…Your hands and feet.” Cyndi tried to grasp the new reality that flesh-eating disease had changed her life forever. Her recent memories of being a successful business manager and new mom seemed oceans away. It just couldn’t be true. I tried to speak, but no words came. Please God—let this be a dream.

Aos 22 anos, um acontecimento inesperado tornou Andrea Schwarz em uma pessoa com deficiência, desafiando seus sonhos e projetos para o futuro. Enfrentando as barreiras impostas pela sociedade, a autora transformou seus desafios em asas. Com coragem, disciplina e uma pitada de rebeldia, ela enfrentou as dificuldades e demonstrou que é possível construir uma vida admirável e alcançar realizações significativas.

I finished my first book, Multiple Sclerosis: A Blessing in Disguise, around the end of 1998. At that time, I was going through a lot of issues that I thought were very important to me. That book told of my discovery, my eventual acceptance of the illness, and how I dealt with what was happening to me. Like anybody else who is faced with the burden of discovery, I had a lot of questions that I felt I really needed to answer, but I never sought to answer why this had happened to me.

Written by Mark Holt-Rogers, a Wellbeing Specialist with over a decade of experience living with Parkinson’s, Shaken is one of the most insightful and practical Parkinson's audiobooks available today. Designed for patients, families, friends, and caregivers, this essential guide draws from Mark’s personal experiences and expertise to provide actionable strategies and emotional support for managing Parkinson’s disease.

"If you can dream it, you can do it!" - das ist bei Oliver Brünner keine Floskel. Dabei sah im Leben des heute erfolgreichen Speakers eigentlich alles ganz anders aus. Noch während seiner Geburt zieht sich die Nabelschnur seiner Mutter wie eine Schlinge um seinen Hals, weswegen er fortan mit einer spastischen Tetraparese lebt. Doch Oliver trotzt den vermeintlichen Widrigkeiten und kann heute auf einen Lebensweg zurückblicken, den dem schon früh als "Sorgenkind" titulierten Jungen wohl niemand zugetraut hätte. Seine Geheimwaffe: das Träumen.

Kathleen O’Neill courageously chronicles her journey through the turbulent realms of bipolar disorder, addiction, and recovery. With raw honesty and resilience, Kathleen shares the battles she fought within herself and against social stigmas, laying bare her struggles, triumphs, and the moments of grace that shaped her healing. This memoir offers a compelling look at the complex layers of mental health , the strength of the human spirit, and the transformative power of hope.

Life with Louie is a collection of coming-of-age stories about growing up with a brother who happens to have been born with Down syndrome. For the author, Mia Rotella-White, having a sibling with a disability never created hardship. The opposite is true. Growing up with Louie meant Mia’s days were full of disco balls, group hugs, fashion shows and dance parties. When adversity struck, and it did, the siblings reminded each other how ridiculous it was to think any tragedy could ever be bigger than their love.

An upcoming book to be published by Penguin Random House.

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.

Wayne Magee is on a mission to empower those who have been repeatedly told, “You can’t!” He has spent his life overcoming obstacles and negative labels intended to convince him that he could not lead a purposeful, fulfilled life. At birth, he was diagnosed with cleidocranial dysplasia, which is a rare genetic skeletal disorder that affects one in one million people. Countless medical professionals stated that he would not live beyond two years old. Wayne’s story demonstrates that for every tough blow, we have an innate ability to overcome societal and medical challenges.