検索キーワード： 障害者

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.

Life doesn’t ask if we’re ready. It simply happens and then it watches what we do next. I was born blind, and from the beginning, the world carried quiet expectations about how small my life should remain. But I refused that script.

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.

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.

True stories, especially miracles, are the best kind. They give us a reason to believe in ourselves, in others, in good, and mostly, reason to believe in God. After decades of trauma, loss, abuse, and severe autism, one mom decided to give up on experts and suffering and believe in miracles. So she got one. The prison doors that had trapped her son for over two decades were opened, and through his faith and sight, she was given hers. In the ashes of life they found out that faith in God was capable to do more than they could imagine, more than was possible.

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.

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.

Your boss asked you for a chat, and you just knew you were going to be fired You didn't sleep all weekend, and you weren't fired Someone answered your message with a thumbs-up emoji and you just knew they hated you. So you stopped talking to them, they eventually stopped texting, and now you...

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 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.

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.

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.

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.