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 Ding Yuan (L) and Pan Longfei take a body training during an acting workshop for "Rare Hug", a drama on rare diseases, at Beijing Tianqiao Performance Arts Center in Beijing, capital of China, Feb. 21, 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)

       1 2 3 4 5 6 7 8 9 10 Next   >>|

    KEY WORDS:
    EXPLORE XINHUANET
    010020070750000000000000011100001378582011
    主站蜘蛛池模板: 黑人性受xxxx黑人xyx性爽| 国产精品嫩草影院人体模特| 天天摸天天干天天操| 国产综合激情在线亚洲第一页| 国产精品久久久久毛片真精品| 国产在线午夜卡精品影院| 国产99视频精品免视看7| 人人澡人人透人人爽| 亚洲国产品综合人成综合网站| 久久在精品线影院精品国产| 一区二区三区日韩| 2022国产成人精品福利网站| 丁香婷婷亚洲六月综合色| 美国十次狠狠色综合av| 永久免费AV无码网站YY| 日韩一区二区三区精品| 天天爱天天做色综合| 国产成人女人在线观看| 北条麻妃一区二区三区av高清| 亚洲欧美乱日韩乱国产| 久久午夜羞羞影院免费观看 | 免费一级欧美大片在线观看| 亚洲一级毛片免费观看| 中国少妇无码专区| 污视频免费网站| 精品特级一级毛片免费观看| 欧美一级黄色影院| 开心久久婷婷综合中文字幕| 国产精品538一区二区在线| 又黄又爽又色又刺激的视频| 亚洲啪啪AV无码片| 一本大道无码人妻精品专区| 免费人成在线观看69式小视频| 精品国产欧美精品v| 杨晨晨白丝mm131| 天天干天天射天天操| 国产亚洲午夜精品| 亚洲国产欧美日韩一区二区| 一级成人a毛片免费播放| 精品福利视频网站| 永久免费bbbbbb视频|