We found out Emma has Crohn's disease. We spent a week at Children's Hospital. In the end, the therapy we chose was a slow drip night feed. This will be something she will be doing for a long time. We are happy she doesn't have to have steroids. She wears an NG tube for now and we are hopeful the therapy is working and we can get a G tube placed soon. She has been brave. There have been a lot of pokes, pills, and things being placed in very uncomfortable places...but she has done all the Doctors have asked her to do, and for that we are very grateful parents.
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