検索キーワード： 制作 "--Tyson Hanks" 障害者

Blind War by Tamer Zaid is a compelling autobiography that recounts the author's journey through adversity as a blind Palestinian navigating life in America. It chronicles his battles with internal and external conflicts, from health challenges like leukemia and blindness to cultural identity struggles and societal expectations. Tamer's story is one of resilience, self-discovery, and finding strength amidst chaos. It highlights the unwavering support of family, the resilience of the human spirit, and the power of faith and determination to overcome life's most daunting obstacles.

Born with Epidermolysis Bullosa (EB), a rare and excruciatingly painful condition that makes her skin as fragile as butterfly wings, Emma Fogarty was not expected to survive infancy. Today, at 41 years of age, she is the oldest living Irish person with the condition, continuing to defy the odds with extraordinary strength, resilience and remarkable achievements. However, every accomplishment Emma makes comes with its own set of obstacles.

Damiano è un ragazzo grande, grosso e con pochi amici perché ama passare le sue giornate facendo cose che gli altri ragazzi non capiscono, come fissare il turbinio vorticoso della lavatrice o giocare per ore con i coperchi delle pentole di sua nonna. Ma la sua vera passione è quella per la musica, soprattutto classica, visto che vorrebbe diventare un cantante lirico. Anche se ama pure il jazz, la musica da discoteca, la dance, la techno e chi più ne ha più ne metta. Tranne la musica rock, quella che invece sua sorella minore Margherita ascolta a tutto volume nella stanzetta accanto.

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.

Gracie wrote Comfort in Darkness after being diagnosed with Parkinson’s Disease, a terminal sentence which he views as the greatest fight of his life, one he knows he will eventually lose. This is Gracie’s defining life statement about his spiritual and technical practice. For the first time, he reveals his time-tested theories and techniques of invisible Jiu Jitsu, a combat system anyone can use to awaken their power and apply it to their everyday lives. An indispensable tool for any fighter or seeker, Comfort in Darkness teaches how to balance and align the mind, body, and spirit.

Raymond Antrobus was first diagnosed as deaf at the age of six. He discovered he had missing sounds—bird calls, whistles, kettles, alarms. Teachers thought he was slow and disruptive, some didn’t believe he was deaf at all. The Quiet Ear tells the story of Antrobus’s upbringing at the intersection of race and disability. Growing up in East London to an English mother and Jamaican father, educated in both mainstream and deaf schooling systems, Antrobus explores the shame of miscommunication, the joy of finding community, and shines a light on deaf education.

For years, renowned ethics scholar Deni Elliott lived with her own moral dilemma: though severely visually impaired since birth, she spent decades attempting to "pass" as sighted, often finding ingenious but problematic workarounds in the process. Everything changed in her 40s when an ophthalmologist diagnosed her as legally blind and she could no longer hide her impairment. To maintain her independence, she would need to use a guide dog and openly present as disabled–a label she had rejected for decades.

Almost 10 years after learning that her son is autistic, Julie Green was also diagnosed, shedding light on a lifetime of feeling othered and misunderstood. Motherness traces Julie's journey from childhood to early motherhood, when she must advocate for her son while navigating her own struggles. With more girls and women being diagnosed in the last decade—many of them later in life—the face of autism is changing. Motherness provides a rich, intensely personal account of what it is like to be autistic through the lens of both a mother and child.

As two siblings, we were walking toward the light. In our mind's eye, it shined brightly, that green light of hope, as multiple sclerosis greatly impacted our lives. We accepted help along the way but not as a sign of defeat. A disabled person is seen as a burden and unfortunately is treated as such. The world doesn't have the patience or understanding of the tremendous struggle one bears living in a world not meant for frailty. This has been a journey of many decades. MS can lead to other health challenges that are formidable in and of themselves, like JC virus or PML.

Phyll Zone spent a lifetime feeling lost. Labeled “lazy,” “spacey,” and “careless,” he struggled in a world that refused to speak his language. The constant storm of ADHD and the silent sabotage of dyslexia weren't just academic challenges; they were emotional earthquakes that shattered his self-worth. Lost in Translation is more than a memoir—it’s a revelation. It’s the story of a late diagnosis that finally provided the map to a bewildering mind, transforming a lifetime of shame into a powerful new identity.

If you grow up in a world where wrinkles are practically illegal, going bald is cause for a mental breakdown, and women over size zero are encouraged to shoot themselves (immediately), what the hell do you do if you're, gasp... disabled? Whatever body you’re born into, the pressure to be normal is everywhere. But have you ever met a normal person? What do they look like? Where do they live? What do they eat for breakfast? And what the **** does normal mean anyway?

先天性疾患を持って生まれ、「生まれた時から歩けなくなることは分かっていた。」という彼が、１２歳で車いすユーザーになり、車いすバスケに出会い、銀メダルを獲るまでをまとめたヒューマンエッセイ。

Close your eyes and get ready to see the world in a new and more positive way. As a child in Toronto, Molly Burke was diagnosed with retinitis pigmentosa and became completely sightless as a teenager. Now an award-winning YouTube star and global influencer, Molly shares what it’s like to be a purple-haired, pink-obsessed fashion and makeup lover in a seeing world. She speaks with authenticity and candor about how she tackles the preconceived notions we have around blindness; Molly has made it her mission to make us see her - and ourselves- in a wholly empowering way.

According to the Center for Diseases Control, 133 million Americans—one out of every two adults—have at least one chronic illness, and half of these are women. While many of these individuals finally have a diagnosis, and are no longer “sick”, they’re still not “well.” They’ve gone through the treatments, taken the medications, and yet still find themselves suffering. So, what do you do after you’ve discovered the root of your condition, and you’re still not healed?

After a failed spinal surgery left him broken, Dr. Bhaskar Bora found himself facing a death-in-life: stripped of his identity, his independence, his ego. But in the ashes of collapse, a new truth emerged — one revealed in both the Bhagavad Gita and the paradoxes of quantum science: that consciousness cannot be destroyed, that suffering can be a teacher, and that brokenness itself can become the doorway to wholeness.

Fetal alcohol spectrum disorder (FASD) affects up to 1 in 20 people, and is particularly prevalent among young people in the adoption and fostering system. As a hidden brain injury, FASD can manifest in ways that often lead to challenging behaviors, which can feel overwhelming for caregivers relying on traditional parenting strategies. In this supportive guide, Barb Clark shares her experiences raising a child with FASD - what she got wrong, what she got right, and what you can do to support your own family.

Andreea, giovane universitaria, arriva ad Alessandria dalla Romania per proseguire gli studi. Inaspettatamente, dopo pochi mesi, a Genova conosce Paolo, si innamora e di lì a un anno nasce Elena. A poco più di un anno di età la bambina inizia ad accusare sintomi di cui non si conosce l'origine. Per i genitori comincia un viaggio pieno di incertezze, ricoveri e preoccupazioni fino alla diagnosi di una rarissima malattia genetica.

Mike grew up on a tree farm in Missouri and spent his childhood on horseback with dreams of becoming a cowboy. The connection he formed with horses shaped his earliest understanding of freedom and purpose. But as adulthood beckoned, he traded his saddle for a suit, building a thriving career and raising a family while his childhood aspirations faded into memory. When a devastating diagnosis of a rare genetic neurological disease struck in his mid-thirties, everything changed.

This intimate memoir reveals the woman inside one of autism’s most prominent figures, Jennifer O'Toole. At the age of 35, Jennifer was diagnosed with Asperger's syndrome, and for the first time in her life, things made sense. Now, she exposes the constant struggle between carefully crafted persona and authentic existence, editing the autism script with wit, candor, passion, and power. Her journey is one of reverse-self-discovery not only as an Aspie but - more importantly - as a thoroughly modern woman.

This is the biography of a young man with some neurological differences, written in the first person. Through his eyes, we see how he perceives his life and negotiates his reality. His world and his understandings of life may be different from the norm, but we learn to appreciate a special type of soul that should be acknowledged and celebrated as part of human diversity. This book demonstrates the love and nurturance of his mother and the dynamics of his relationship with her. We also enjoy hearing about the comfortable lifestyle that Marcelo has been given, including his worldwide travels.