検索キーワード： 障害者

Born in 1940, Author Sam McNair always believed that life would never be fair toward black men who struggled to be normal. After years of standing out like a sore thumb, Sam finally met someone who was quite like himself and diagnosed himself with Autism but not long afterwards did regain control of his life and now living his best one at 81 years young. Listen to Sam's experience with how he coped with people around him and all of the beautiful women involved in his transition back to an all time playboy.

MIND ESTRANGED tells the story of Bethany’s life, from her years as a promising university student through her gradual descent into schizophrenia, and unexpected, full recovery. While slowly losing her sanity, she traveled the world. She returned to the U.S. unable to work or study—and soon found herself homeless, delusional, and controlled by voices that talked to her and gave her orders in her mind. Bethany’s memoir enables the listener to enter into the mind of a person with schizophrenia, homeless and roaming the streets.

From an author with a psychology background, a candid memoir about the interior of her own psychotic episode. After the culture shock of moving from a small Wisconsin town to the tumult of Los Angeles in 1967, Linda’s family disintegrates: her parents decide to divorce, and she and her younger brother, Brian, suddenly must fend for themselves. While she finds a foothold in academic pursuits, Brian spirals downward into schizophrenia and, finally, commits an irrevocable act.

Grow Against All Odds, With Unshakeable Confidence is the story of Dr. Anand Modi. It is the tale of a man who worked to have it all and then found himself hanging over the jaws of death after a life altering stroke. Full of details about how he clawed himself out and acquired a new lease on life, the book is a mix of survival, self help and business advice. Its 15 chapters are split in a unique way. Chapters 1 and 2 introduce Anand’s background and the medical drama.

The stories in this book are about women who are married to, or were once partnered with, men on the mild end of the autism spectrum, formerly known as Asperger’s syndrome. These women are not autistic, so their relationships are considered neurodiverse (meaning there’s a neurotypical person in a relationship with a neurodivergent person). The focus within the stories is Cassandra Syndrome. A very life-altering phenomenon that often occurs—and usually remains unaddressed—within these relationships.

This memoir was written to honor my youngest brother’s influence over my life—the good, the bad, and the ugly, of living with a Down Syndrome sibling. It tells the story of the children of my family, despite our parents’ frailties, remaining committed to each other through life’s many changes and separations. Who I am today is directly related to who I needed to become.

The moving true story of Linda Crosby, an accident survivor who was left permanently and totally disabled, and Roy Crosby, her devoted husband and caregiver, The Day My Life Changed: An Accident Survivor offers a glimpse into the lives of an everyday couple whose love endured and thrived, even in the most impossible odds.

Born 10 weeks premature and given only a 10 percent chance of survival, Rene entered the world fighting for her life. Diagnosed with cerebral palsy, she grew up navigating a society that often defined her by limitations rather than potential. But this audiobook tells a different story—one of determination, courage, humor, and an unshakable belief in the power of being heard.

This book is for the girl who disappeared while trying to be everything for everyone — and lived to tell the truth. The Year I Became a Muse is not a memoir written from hindsight. It is a rebirth told in real time. Through raw moments, quiet revelations, and divine interruptions, Diana Zaitseva documents the season when survival became self-knowing — when grief softened into clarity, and chaos gave way to grace. This audiobook captures the unfiltered inner dialogue of a woman learning how to stay, how to listen, and how to rebuild from the inside out.

At 14-years-old, Karen Oliver’s son Ben was diagnosed with Friedreich's Ataxia, a rare genetic disorder affecting coordination and mobility and causes the development of cardiomyopathy and associated arrythmias. She was told he would be wheelchair bound by seventeen and live no longer than 34. But Ben was not going to let that stop him.

Total blindness had suddenly descended on her as she walked to her Christian spirituality class one morning. To make matters worse, her professor challenged the class, saying, "Why should we believe in God?"

Blame: Death, Disability, and the Search for Justice for Guy Mitchell attempts to find meaning and justice in the tragic death of a vulnerable individual whose circle of care failed him. Dramatic nonfiction that sounds like a legal thriller, Blame resists easy answers, exposing a tangled web of negligence, indifference, and systemic failure and probing the deeper structural forces behind Guy's death. What emerges is a powerful indictment of a broken system and a strong argument that the duty to care for society's most vulnerable ultimately lies with us all.

This is an enhanced edition of the author's original memoir published in 2021. It includes an updated Author's Note, as well as a glossary of ADHD and recovery related terms and a Resources guide designed to educate the listener and provide support. The memoir was inspired by the author's struggles with misdiagnosed and misunderstood attention deficit hyperactivity disorder (ADHD), as much as it was fueled by her passion for adventure and escape through music and (later) alcohol and marijuana.

In Unbreakable(ish), Ali Ingersoll takes you on a wild, hilarious, and deeply real ride through a life that broke multiple times—then got rebuilt stronger until one minute, she was traveling the world—the next, she was paralyzed from the chest down, directing her own emergency rescue and questioning everything she thought she knew.

At age 24, Janet Buttenwieser moved to Seattle with a résumé devoted to public service and fantasies of single-handedly ending poverty. But within a year she’d developed an intestinal illness so rare she wound up in a medical journal. Janet navigated misdiagnosis, multiple surgeries, and life with a permanent colostomy. Like many female patients her concerns were glossed over by doctors. She was young and insecure, major liabilities in her life as a patient. How would she advocate for low-income people when she couldn’t even advocate for herself?

When Joni was paralyzed in a diving accident at the age of seventeen, she quickly understood her life would never be the same. But what she didn't know was how God would use her story to affect the lives of millions of people from across the globe. This little book is full of biblical truths and important lessons Joni has learned along the way. No matter your situation, you'll be encouraged as you discover Jesus' faithfulness in the midst of life's challenges.

Barbara Melvin has a secret to her success: her five Ps. And never were they more important than the day she woke up in her Naples, Florida home, blind. In the blink of an eye, life changed.

Chronically Awkward is not a story told for sympathy — it’s a story told for truth. It is a raw, unfiltered account of one person’s lifelong attempt to exist in a world that keeps insisting on rules he never agreed to play by. Jason takes listeners through the tangled intersections of autism, ADHD, trauma, and chronic illness — through the systems that failed him, the people who shaped him, and the quiet victories that kept him here. It’s both memoir and mirror; a reminder that surviving isn’t the same as living, and that sometimes we only find who we are after everything else falls apart.

In this deeply moving memoir, L.A. Batista recounts her incredible journey through a life filled with obstacles — family turmoil, physical challenges, an abusive marriage, and single parenthood. Despite the hardships, her story is one of unyielding strength and resilience. Beginning with her childhood in the 1960s in a neighborhood in New York City, the author recounts her family life as she dealt with an undiagnosed rare disease.

Lorsqu'on rencontre Martin pour la première fois, ce qui frappe immédiatement, c'est son sourire charmeur, son enthousiasme, son oeil qui pétille, son aisance à l'oral et ses idées qui fusent dans tous les sens. Son fauteuil, on n'y pense même pas. On ne le voit pas. C'est tout juste si l'on remarque que ses doigts, qui paraissent pourtant si agiles, sont inertes, tant Martin a de choses à partager, d'anecdotes à raconter et de montagnes à déplacer. Pourtant, Martin est tétraplégique.