検索キーワード： 障害者

Cosa significa vivere con un cervello che corre più veloce del mondo intorno? In questo libro, Luca Donato racconta con ironia e sincerità la sua vita con il disturbo da deficit di attenzione e iperattività, l'ADHD: un continuo equilibrio tra entusiasmo e fatica, creatività e disordine, energia incontenibile e sensi di colpa. Dall'infanzia irrequieta agli imprevisti quotidiani, dalle sfide sul lavoro alle relazioni affettive, l'autore ci accompagna in un viaggio fatto di inciampi e scoperte, mostrando come la diagnosi non sia un punto d'arrivo, ma l'inizio di una nuova comprensione di sé.

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 Autistic Girl Went to Japan is the inspiring story of a young woman who moved halfway around the world in pursuit of happiness. With humor and remarkable candor, Bianca describes the challenges of applying for a visa during a time of terrifying uncertainty, slogging through endless red tape, and the loneliness that comes with being a stranger in a strange land. Oh, and how she wound up evicting a bat from her new apartment, attending a Pokémon GO event with a bunch of middle-aged women, and discovering the best thrift store in all of Tokyo.

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.

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.

Written by a hugely popular actor and autism advocate, this book is for neurodiverse Gen Z-ers looking for an inspirational mix of real-life advice with a heartfelt personal story. Are you autistic, or think you might be? Are you ready to not only understand but embrace your unique mind?...

Hülya wird mit einem Gendefekt geboren, ihre Hände und Beine sind nicht voll funktionsfähig. Trotzdem lässt diese starke Frau sich nicht unterkriegen und meistert ihr Leben mit all seinen Hindernissen. Hülyas Lebens- und Liebesgeschichte zeugt von ihrem unerschütterlichen Glauben an das Gute. Mit ihrer warmherzigen Art berührt sie die Menschen überall, wo sie hinkommt.

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.