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65 Redroses
''65_RedRoses'' is a 2009 documentary film about Eva Markvoort, a young woman from New Westminster, British Columbia, who suffered from cystic fibrosis. The film follows Markvoort as she lives her life undaunted by her disease, waiting for a lung transplant while blogging about her experiences.
==Production==
The film began when Philip Lyall, a long-time friend of Markvoort, introduced her to his University of British Columbia film school partner Nimisha Mukerji. Lyall and Mukerji had been looking for a post-graduation project and decided to chronicle Markvoort’s wait for a double-lung transplant. They named the film ''65_Redroses'' after Eva's online identity, which she had chosen because, according to the Canadian cystic fibrosis community, "sixty-five roses" is how many young children with the disease mispronounce “cystic fibrosis”. Eva added 'red' because it was her favourite colour.
When Lyall and Mukerji began shooting, Markvoort’s lungs were so clogged doctors said that without a transplant, she would not live to 2009. She was getting ready to visit a pumpkin patch the week before Halloween in 2007, when her pager went off, a signal to call the hospital transplant center. A pair of lungs was available for transplant. This sequence, emotional for both Markvoort and the filmmakers, was instrumental in attracting the attention and backing of the Canadian Broadcasting Corporation.〔
抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』
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