検索キーワード： 障害者

The medical system took twelve years to reluctantly agree with Fay Martin that her husband was sliding into dementia. Even after he died three years later, people still questioned the diagnosis. This is an audiobook about what happens behind that veil of invisibility. Dementia Widow exposes, with courage and candor, the poison that seeps in, as a healthy reciprocal marriage becomes inexplicably hierarchical. Only when dementia is recognized as the villain does the relationship morph to offer the loving caregiving that enables a good final chapter.

A Life in Too Many Margins is a literary episodic tale featuring David, an autistic, chronically ill, and deeply exhausted queer individual. He's survived a few too many doctors with God complexes and an education system that couldn't accommodate a paper cut, let alone a brain like his. Now he's trying to keep it together long enough to get out and figure out what a life outside of survival mode even looks like.

This book contains raw, unfiltered testimony from a life shaped by childhood trauma, poverty and chronic pain. It moves in fragments — from car to bed to memory — documenting survival rather than offering inspiration. Written and narrated by the author, this audiobook preserves the voice exactly as lived.

Questo libro nasce dal bisogno di raccontare la quotidianità di una famiglia per tre quarti neurodivergente: e così, tra compiti a ostacoli e lettere che si rincorrono, prende forma un racconto vivo, umano, che mescola il memoir al consiglio pratico, l'esperienza personale alla riflessione condivisa; senza la pretesa di insegnare, ma con il desiderio di offrire uno spaccato di vita e uno sguardo onesto su ciò che significa convivere con la dislessia - da genitori e da figli -, affrontando le difficoltà ma anche valorizzando le risorse, i talenti, le prospettive diverse.

Adaptive Frequencies is an abstract autobiographical account of life shaped by multiple traumatic brain injuries. The narrative explores the physical, cognitive, and emotional challenges of TBI, as well as the ongoing process of adaptation required to live with a brain injury-related illness. With the goal of raising awareness, the book highlights a range of multidisciplinary treatments and supportive resources encountered along the way. These are woven into the narrative and supplemented by a succinct resource list in the appendix for readers seeking further information.

This is my personal story of battling leukemia as I entered my so-called “golden years.” Turning 65 marked the beginning of a series of profound changes, brought on by both family struggles and personal health challenges. Eventually, I was diagnosed with a rare form of leukemia. I endured grueling chemotherapy, fought through debilitating side effects, and then faced yet another blow — new heart complications and the looming possibility of a second, entirely different cancer.

Voices of Women 2025, Vol. 4 is more than a book, it's a movement. Compiled by international speaker and community builder Kimberly Crowe and published by Woodhouse Publishing, this powerful anthology gathers the stories of women from across the globe who dared to rise, reclaim their voices, and create change in their lives, their communities, and the world.

When twenty-nine-year-old Christine Schrader was diagnosed with stage four colorectal cancer, she refused to let fear or statistics define her. Instead, she opened her heart—and her journal—sharing the raw reality of treatment, the strength of family, and the stubborn joy she found in small, everyday moments. How Cancer Improved My Life is Christine’s story in her own words: candid, faith-filled, and often laced with the humor that carried her through more than sixty rounds of chemotherapy.

In Stronger Than Bone, Greg takes listeners on a journey that defies medical odds and redefines resilience. From childhood trauma to hard-won triumphs, his memoir is a testament to the power of determination, joy, compassion and love—even when the world tells you to give up.

Hallo, ich bin eine Autistin im "Spektrum" und erfuhr es erst mit 30 Jahren! Natürlich war ich bei einem Spezialisten, denn zu Anfang konnte ich mir nicht vorstellen, tatsächlich eine Autistin zu sein. Denn ich hatte keine Ahnung von Autismus. Das was ich las, gefiel mir nicht. Um es kurz zu machen, ich wollte keine Autistin sein, bin es aber und es war ein heftiger Schock, behindert zu sein, ohne es gewusst zu haben. Neben dem Schock, fühlte ich mich schrecklich alleine und irgendwie von mir selbst im Stich gelassen. Denn ich lebte ein Leben, womit ich nicht klar gekommen bin.

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.

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.

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?"