Is 1 Litre of tears based on a true story?
“1 Litre of Tears”; also called A Diary with Tears or A Diary of Tears) is a 2005 Japanese television drama for Fuji Television, based on a true story of a 15-year-old girl named Aya Kitō, who suffered from degenerative disease and died at the age of 25.
Is ASOU a haruto?
The character of Haruto Asou, who is Aya’s only love interest, is completely fictional. There was no Haruto in real Aya’s life. Haruto’s character was added at the request of her family, that even if she didn’t get to have a hero in real life, she should have one at least on screen.
Is 1 Litre of tears sad?
1 litre of tears is a very touching story about a young girls struggle with a very cruel disease. A disease which takes away all the things she loves, one by one. As Aya-chan struggles, all people around her are struggling with her. Share the pain, sadness, but also love and joy with aya’s family.
What disease did Aya have?
Later, doctors diagnosed her with spinocerebellar ataxia, an intractable disease that gradually deprives a person of freedom of limbs and speech and eventually causes the loss of all motor functions of the body.
Who voiced Aya in AC origins?
Alix Wilton Regan
The podcast consisted mostly of an interview with voice actresses Alix Wilton Regan and Zora Bishop, who played Aya/Amunet and Cleopatra in Assassin’s Creed Origins, respectively.
What is Marie’s ataxia?
Signs and symptoms Spinocerebellar ataxia (SCA) is one of a group of genetic disorders characterized by slowly progressive incoordination of gait and is often associated with poor coordination of hands, speech, and eye movements.
Why was Aya not the main character?
Though the strong-willed warrior is playable for several missions throughout the game, Aya is undoubtedly overshadowed by her husband Bayek. Aya’s role gradually shrunk over the course of Assassin’s Creed Origins’s development, but Aya was originally meant to become the main protagonist, according to Bloomberg.
How rare is SCA?
Spinocerebellar ataxia (SCA) is a progressive, degenerative, genetic disease with multiple types, each of which could be considered a neurological condition in its own right. An estimated 150,000 people in the United States have a diagnosis of spinocerebellar ataxia at any given time.
What causes Machado Joseph disease?
The disease is caused by a mutation in the ATXN3 gene, which is located on chromosome 14q (14q32. 1). In exon 10 the gene contains lengthy irregular repetitions of the code “CAG”, producing a mutated protein called ataxin-3. (Normally, the number of copies is between 13 and 41.)