Drama on rare diseases played by patients, relatives staged in Beijing

    Source: Xinhua| 2019-02-28 21:18:19|Editor: ZX
    Video PlayerClose

    (FOCUS)CHINA-BEIJING-RARE DISEASE-AWARENESS-DRAMA (CN)

    Rare disease patients Cai Li (2nd L) and Cui Ying (1st R) have their facial make-ups applied before their performance in "Rare Hug", a drama on rare diseases, at Beijing Tianqiao Performance Arts Center in Beijing, capital of China, Feb. 27, 2019. "Rare Hug," a Chinese drama on rare diseases, was staged at the Beijing Tianqiao Performing Arts Center Wednesday evening to mark the 12th Rare Disease Day, which falls on Feb. 28, 2019 under the theme "Bridging Health and Social Care." The drama was played by rare disease patients in collaboration with their relatives. Assisted by two volunteer directors, the cast took part in a three-day workshop as well as rehearsals that lasted for two days, before presenting their real-life stories to the audience. Chen Meiping, one of the directors, has devoted herself to the public theatre and related arts since 2005. In late 2018, she worked with Yi'ou Wang, secretary-general of Illness Challenge Foundation, to come up with the idea of telling stories of rare disease patients with a collaborative drama. Before meeting the rare disease patients who volunteered to act in her drama, Chen was not so confident in the final result because they had only limited time for proper training. Chen was later surprised by the collaborating patients' readiness to perform and their desire to share their stories with others. "I am reassured by that desire," said Chen. "It is as if they can act themselves out immediately after they are up on the stage." The other director, Liang Wanyun, had been worried that the patients were amateurs who had not ever performed in a real drama and not sure whether they could go through the acting training in just three days. Yin Yuanyue, a 29-year-old volunteer actress in the drama who is diagnosed with muscular dystrophy, called for increased social awareness of the rare disease patient group. "What I am seeking is a sort of presence, as an actress for instance, that can act as encouragement for fellow patients who are still too afraid to reach for the outside world," she said. "It is particularly rare for a rare disease patient to rise to the stage and speak out for ourselves," said Pan Longfei, a 30-year-old volunteer actor who is diagnosed with Kallmann Syndrome. Subject to long-time isolation and misunderstanding by those around him, Pan hopes his performance could call on fellow patients to be conscious of their true selves and accept life as it is. Although rare diseases are found in a very small number of patients, most of them are incurable. Only five percent of rare diseases can be treated with medicine. About 80 percent of the 6,000 to 8,000 rare diseases known to us are gene-related, with more than 50 percent of them appearing in early childhood. According to World Health Organization (WHO) statistics, rare diseases affect a population of about 400 million worldwide, which means that for every 15 people there is one rare disease patient. Whereas in China, the number of people suffering from rare diseases is estimated to top 20 million. There are more than 100 rare disease patient support groups set up in accordance with disease categories in the country. (Xinhua/Zhang Yuwei)

    KEY WORDS:
    EXPLORE XINHUANET
    010020070750000000000000011100001378582011
    主站蜘蛛池模板: 中文字幕丰满乱子伦无码专区| 亚洲精品第五页中文字幕| 中文字幕中出在线| 少妇精品久久久一区二区三区| 亚洲av永久综合在线观看尤物| 男人的j插女人的p| 国产成人久久精品| 9999国产精品欧美久久久久久| 扒开双腿疯狂进出爽爽爽动态图| 亚洲中文字幕无码日韩| 琪琪see色原网中文| 国产mv在线天堂mv免费观看| 亚洲精品一二区| 在线视频精品一区| 中文字幕.com| 日韩精品无码一区二区视频| 亚洲精品伊人久久久久| 精品视频一区二区三三区四区 | 国产色视频一区二区三区QQ号| 中文字幕不卡在线观看| 最新浮力影院地址第一页| 亚洲精品成人a在线观看| 美国免费高清一级毛片| 国产午夜无码福利在线看网站| 2021国产精品久久久久| 天天狠天天透天干天天怕∴| 中文字幕欧美一区| 日韩精品在线一区二区| 亚洲影院adc| 男人扒开女人的腿做爽爽视频| 国产一区二区三区不卡观| 激情五月婷婷色| 国产精品青青青高清在线观看| tube欧美69xxxx| 成人精品一区二区三区中文字幕| 国产人妖在线播放| 18禁男女爽爽爽午夜网站免费| 天天躁夜夜躁狠狠躁2021| 中文字幕在线观看你懂的| 日韩电影中文字幕在线网站 | 亚洲综合区小说区激情区|