我的儿子乔尼出生时双脚畸形,医生向我们保证说经过治疗,小乔尼能像正常人一样走路,但像正常人一样跑步的可能性则微乎其微。乔尼3岁之前一直在接受治疗,和支架、石膏模子打交道。到他七八岁时,他走路的样子已让人看不出他脚有毛病。邻居的小孩子们玩游戏的时候总是跑过来跑过去的。毫无疑问小乔尼看到他们玩就会马上加进去跑啊闹的。我们从不告诉他他不能像别的孩子那样奔跑,我们从不说他和别的孩子不一样。因为我们不对他说,所以他不知道。 My son Jonny was deformed at the time of her birth. The doctor assured us that after treatment, Jonny Jr. could walk like a normal person, but the possibility of running like a normal person was minimal. Jonny had been treated before the age of 3, dealing with stents and plaster molds. By the time he was seven or eight years old, the way he walked had caused people to see that he had problems with his feet. The children of neighbors always ran over to run the game. There is no doubt that Little Jonny will see them play and they will be added and run. We never tell him that he cannot run like other children. We never say that he is different from other children. Because we did not speak to him, he did not know.