前不久,患有心脏怪病的天生残疾孩童叶川儿,在其父亲的陪护下,从海口美兰机场登上了航班飞往北京,然后将从北京转机飞往美国纽约,接受纽约州立大学医疗中心的治疗。叶川儿能实现赴美治奇症的愿望,这是社会各界大力支助的结果。1998年2月3日,叶川儿出生于海南省海口市。他一生下来就患有先天性心脏畸形、胸前左侧胸壁缺损、单心室、肺动脉狭窄、三尖瓣少量返流、可疑大血管、转位并右房心包部分缺损等国内外非常罕见的疾病,成了天生残童,生命危在旦夕。当年11月,叶川儿的父亲在跑遍了国内的大小医院均告无法治疗后,只得在网上向外界求救。1999年9月,美国“格尼瑞亚希望之地”慈善 Not long ago, Ye Chuan-er, a disabled child with a strange heart disease, boarded a flight from Haikou Meilan Airport to Beijing under the escort of his father and then flew from Beijing to New York, USA, accepting a contract from New York State University Medical center treatment. Ye Chuan Er can achieve the goal of treating chihchis in the United States, which is the result of vigorous support from all walks of life. February 3, 1998, Ye Chuan was born in Haikou City, Hainan Province. He was born with congenital heart malformations, left chest chest wall defects, single ventricle, pulmonary stenosis, tricuspid regurgitation, suspicious blood vessels, transposition and partial destruction of the right atrial pericardium and other very rare diseases at home and abroad , Has become a natural residual children, life at stake. In November of that year, Yechuan children’s father ran in the country’s large and small hospitals were unable to treat, had to help the outside world online. September 1999, United States “Grecia hope ” charity