"但是他是我的孩子，无论他长得什么样，我都会像我母亲爱我一样无条件地爱他。"

"My only wish is that my child will grow up like a normal child. We were locked away becausepeople couldn't cope with the way we looked. I only hope people will be different and kindertowards my son."

"我唯一的愿望就是我的孩子可以像正常孩子一样健康成长。因为人们不知道该如何面对我们的容貌，所以我们曾被他们所疏远。我只希望人们能够以不同的方式，或者更加善良地对待我的儿子。"

There is no known cure for Werewolf Syndrome and all Manisha and her sisters have been ableto do is slather themselves in removal cream every few days.

目前狼人综合症还没有已知的治疗方法，玛尼沙和她的姐妹现在能够做的只能是每隔几天就涂上厚厚的脱毛膏来脱毛。

Manisha and husband had an arranged marriage on May 25, last year, and are overjoyed atbecoming parents but Manisha's mother-in-law is devastated her grandson has the WerewolfSyndrome.

玛尼沙和她的丈夫在去年5月25日由包办婚姻而结合到一起，他们很高兴能够为人父母，然而玛尼沙的婆婆对于孙子患有狼人综合症一事感到极为震惊。

"My husband is very supportive and loves his son but my mother-in–law is not happy," Manishasaid.

【5个月大男婴身负狼人基因 家族遗传令母亲心碎】相关文章：

★ 娱乐时尚:大球换小球 小贝高尔夫球场遇尴尬

★ 不同地区星巴克拿铁的价格差异

★ [娱乐时尚] 09全球青年富翁榜前五位

★ 美国人的假期与工作

★ 福布斯全球最高身价模特盘点(上)

★ 看完小贝大儿子17年的人生，我哭晕在厕所

★ 第88届奥斯卡完整双语获奖名单

★ 娱乐时尚:萨科奇大汗淋淋纽约晨跑

★ 狗尾非要续貂，论影视行业的“续集病”

★ 娱乐资讯:千真万确:杰克逊头发变钻石