Zeigt Titel in Menschen mit Behinderung

Life With Jefferson tells the true story of the remarkable partnership between Jefferson and Penny Leclair, a deafblind woman whose independence depended on finding the right guide dog. After two years of searching, Jefferson was chosen for his unique intelligence, sensitivity, and ability to meet Penny’s specific needs. His training continued with special considerations that shaped him into more than a working dog—he became a trusted partner and beloved family member.

Getting Legless is the memoir by Jared Hughes, who was diagnosed with Chronic Kidney Disease in 2021. As he was getting used to his new life on dialysis and the prospect of having a kidney transplant, his life was further turned upside down when he discovered that he had arterial disease which had been caused by his kidney disease being undiagnosed for so long. This resulted in Jared losing both of his legs.

In November 1991, author Eugen Ehrenberg was diagnosed with multiple sclerosis, and he learned how to manage the imminent limitations in his movements. Twenty years after that, he suffered an accident that left him in the hospital for a long time as he managed to regain part of his mobility. He had to become friendly with his new active wheelchair and later with his hand bike.

The Moment Everything Changed is what makes this book different—it’s not clinical, it’s personal and confrontational. I remember the exact moment I opened my eyes and something was different. Not a little different, everything different. Three decades of pain, illness, disease that created constant noise in my body, mind, and soul to opening my eyes after surgery #21… POOF!!! It was gone. Just gone! Nobody prepares you for that. We spend so much time asking, “Why am I in pain & will it ever stop?” “Why can’t anyone figure it out and just help me?” Tough times...

What does it mean to think differently in a world that wasn't built for your mind? Jake Didinsky is autistic, queer, non-binary, and Jewish. They've spent their life building an operating system to survive—a framework for navigating ethics, systems, and human connection when the default settings keep crashing. The Architecture of Uncertainty is part memoir, part philosophy, and entirely honest.

A breast cancer diagnosis changes everything in an instant. Fear rises, and the future can feel uncertain. In Don't Fear the Storm, triple negative breast cancer survivor Janet Fisher shares her honest and faith-filled journey through diagnosis, chemotherapy, surgery, radiation, and recovery—offering Christian encouragement and hope while revealing how relying on God's presence shaped her response to every challenge.

In Life with Bipolar Disorder Marc Gwin offers an honest and deeply personal look into the daily realities of living with a complex mental health condition. Through heartfelt reflections, journal entries, and moments of raw vulnerability, he shares the challenges, lessons, and unexpected beauty that comes with navigation life between emotional extremes.

From Potential to Purpose is a game-changer, packed with life lessons and practical strategies for overcoming challenges, fostering genuine relationships, and transforming obstacles into opportunities. At its heart lies The CUBE Principle—a simple yet powerful framework for creatively utilizing your best energy to achieve your goals and unlock your potential.

In From Shack to White House, Theo Braddy takes listeners on an unforgettable journey through four extraordinary lives. Each one marked by loss, resilience, and faith. From the dusty backroads of Georgia to the corridors of power in Washington, Theo's story is a powerful testament to what it means to rise again, again, and again.

I strive to create an example of all that I can be so that others in my situation can see disability for what it is. Disability does not separate me from anyone. All people are disabled, and only some are temporarily enabled. Everyone will age. Everyone will need a little help. If people understand this, then all are equal. - Thomas. Thomas is a brilliant student, an advocate for people with special needs, and a loving son and brother. He has a rare form of muscular dystrophy that over a short time leaves him completely, physically helpless.

For readers of The Basketball Diaries, Girl, Interrupted, Beautiful Boy, and Just Kids: A memoir of growing up, soaring, shattering, and recovering Growing up in SoCal in the early 2010s, Nolan Trowe spent his early teenage years living largely on his own, exiled from his family, skateboarding...

In Raised in Silence, Maria Gallucci invites you into the vivid, rarely seen world of growing up as a CODA (Child of Deaf Adults). With humor, heart, and unflinching honesty, she shares what it's like to bridge two cultures from the moment you can walk: the Deaf world of her parents and the hearing world outside their door.

Salifu Sesay was but a toddler when a rebel attacker chose to plunge a machete into his skull. Against all odds, this victim of the Blood Diamond conflict in Sierra Leone, West Africa survived. A few years later, fate continued to intervene and Salifu was placed into the arms of Ann Miller, a woman from Overland Park, Kansas, whose life from that moment on, would never be the same. This is their mother/son love story.

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.

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.

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.