Hello, my name is Kelly i live in Ecuador, my sister has a child who is older than 6 years now and she is born with the apple peel syndrome, she is been operated the day after she was born, and now she lives with with not more than 20cm of intestine, we dont know where to go or where to receive treatment, in our country there are not doctors who really know about this case, what can we do because the girl suffers a lot by vomiting and she does not grow she looks like a 2 years old child