Títulos em Pessoas com Deficiências

Escrito quando Naoki Higashida tinha apenas 13 anos, o conjunto de ensaios reunidos neste audiolivro conta, do ponto de vista do próprio Higashida, a experiência de ser autista. Preso em seu mundo individual, muitas vezes ele exibe comportamentos vistos como estranhos, peculiares, “inadequados”. Seja repetindo palavras e frases aparentemente sem sentido ou evitando contato visual com outras pessoas, Naoki tem uma enorme dificuldade de se comunicar e de socializar.

O sonho de Juli era ser mãe e ela o realizou–e segue realizando diariamente–porém, ela não esperava os desafios que a maternidade atípica lhe reservava. O diagnóstico de Rafael veio no ano de 2015 e, de lá para cá, o hobby de Juli em escrever e influenciar pessoas teve uma mudança drástica: compartilhar tudo aquilo que estava reaprendendo com seu filho e sua família, fazendo-a acrescentar em seu currículo mais uma função: palestrante.

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.

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 the scorching summer of 1989, my second child, a son, entered the world, setting in motion a life-altering journey. Just four months later, a virus thrust him into a hospital, casting an uncertain shadow on our future.

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.

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.

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.