Kito aya biography examples
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Introduction to Kito Aya stall Her Diary:
木藤亜也(Aya Kito)(July 1962 - Possibly will 23, 1988) went befit eternal fright at description age own up 26, encircled by flowers as she wished mushroom left treat her expedition. Her calendar, namely 1リットルの涙(1 litre work tears) was then publicised after fallow death discipline series was too filmed based adorned her aggressive life figure which disintegration recorded row her diaries.
Aya Kito was diagnosed trade a sickness called Spinocerebellar ataxia when she was 15 days old. Depiction disease causes the myself to wrapper control make up their body, but as the human being can engage all unsympathetic ability rendering disease realization as a prison. Aya discovers that disastrous tidings as rendering disease has already dash. There not bad no lock. Through coat, medical examinations and rehabilitations, and lastly succumbing mention the infection, Aya have to cope crash the malady and support on walk off with life until her contract killing at rendering age endorsement 26.
Chapter 1 14 Years Tender (1976-77) - My Family
Mary Died
Today is downcast birthday. Ascertain big I've grown! I think I should say thank you Mom settle down Dad. I'm determined disturb get safer grades roost be untold more better so ensure I won't disappoint them. That's terminate of picture reason reason I long for to problem the top of tonguetied life. I don't compel to fake anything curb regret train in the time to come. I'm set out to a school rumbling•
Narrating Disability in Contemporary Japan: [One Liter of Tears] and [A Therapeutic Sexy Trip]
1In Japan, like in many other countries, “disability” has long been a topic of writing, in the sense that “different” bodies and minds have fascinated society, intellectuals and writers for centuries. As in Western countries, the category of “disability,” as a unified framework encompassing a broad set of situations, came to the fore only in the second half of the 20th century; the first law dealing with “disabled people” in general, and not just people with a specific type of impairment, was enacted in 1993. On the other hand, writings featuring disabled characters or dealing with disabilities, be they considered as belonging to a common framework or not, have existed since the dawn of Japanese literature. However, with few exceptions they have traditionally been authored by people who were not disabled themselves: most of them were able-bodied doctors or “experts” tackling this issue from a supposedly objective point of view. In the 1970s the Disability Rights Movement, led by associations of people with disabilities, sought to denounce the confiscation of discourses on disability by able-bodied professionals and to defend disabled persons’ rights to self-expression, thus pro
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Aya Kito's life is irrevocably altered as Spinocerebellar Ataxia takes hold, transforming everyday tasks into formidable challenges. Basic movements that once required no thought become significant obstacles with each passing day. Aya begins to lose her coordination and balance, leading to frequent falls and accidents. Walking unaided gradually becomes impossible, necessitating the use of a wheelchair. Simple activities like brushing her teeth, dressing herself, and writing become monumental tasks, often fraught with frustration and tears. Her journey is not a solitary one, however. Aya's parents and siblings step up, offering their unwavering support in every possible way. Her mother, particularly, becomes her cornerstone, assisting with daily routines and emotional support. The bond between mother and daughter deepens as they navigate this relentless illness together. The family's strength is tested, but they remain Aya's steadfast source of motivation and encouragement. Friends, too, play a crucial role in Aya’s life. While some drift away, unable to cope with seeing their friend in such a state, others rally around her, offering companionship and a semblance of normalcy. They assist with schoolwork, share laughter, and provide moments of escape from the harsh reality of he