9CaKrnQgWEN作者:hope.huanqiu.comgallery关节挛缩症女孩的正能量生活(组图)/e3pmh4858/e7o8kso2r【环球网综合报道】关节挛缩症(Arthrogryposis)患者四肢无法活动,甚至连手指的活动也十分受限,而患有此病的5岁女孩阿莉莎·婕婷·哈格斯特龙,却给人们留下了完全不同的印象。摄影师詹妮弗·卡其马雷克用三年的时间,记录下了阿莉莎成长的点点滴滴,并于2012年5月,首次公开了其中一部分照片。透过这些照片,人们可以更深入地了解罕见病患者阿莉莎的世界,体会她每日的挣扎与挑战,但最重要的是感受到她具备的惊人毅力。2011年,卡其马雷克以阿莉莎的名义创办了一个非营利组织,期望让人与人之间紧密相连,使人们在精神上受到鼓舞,并感染身边其他的人,同时为阿莉莎以及像她这样患有关节挛缩症的孩子们筹措资金,并提供更好的援助。1377991200000环球网版权作品,未经书面授权,严禁转载或镜像,违者将被追究法律责任。责编:yefang环球网137799120000011["9CaKrnQgWED","9CaKrnQgWEd","9CaKrnQgWDC"]{"gallery":{"members":[{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110431615.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110422431.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110418750.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110420891.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110449931.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110421976.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110437795.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110423613.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110425605.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110426285.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110428608.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110430178.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110433393.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110435652.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110436706.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110439260.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110441240.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110443364.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110445505.jpg"},{"desc":"","url":"\/\/himg2.huanqiucdn.cn\/attachment2010\/2013\/0826\/20130826110447447.jpg"}]}}
【环球网综合报道】关节挛缩症(Arthrogryposis)患者四肢无法活动,甚至连手指的活动也十分受限,而患有此病的5岁女孩阿莉莎·婕婷·哈格斯特龙,却给人们留下了完全不同的印象。摄影师詹妮弗·卡其马雷克用三年的时间,记录下了阿莉莎成长的点点滴滴,并于2012年5月,首次公开了其中一部分照片。透过这些照片,人们可以更深入地了解罕见病患者阿莉莎的世界,体会她每日的挣扎与挑战,但最重要的是感受到她具备的惊人毅力。2011年,卡其马雷克以阿莉莎的名义创办了一个非营利组织,期望让人与人之间紧密相连,使人们在精神上受到鼓舞,并感染身边其他的人,同时为阿莉莎以及像她这样患有关节挛缩症的孩子们筹措资金,并提供更好的援助。