Today is Brayden's sweat test. The gastro thinks we should make sure he doesn't have cystic fibrosis (because he shows the digestive signs, but not all the breathing issues and infections). I think it's just another torture device for my poor child. I have to do it though because I will always worry and wonder if I should have done it. He was already tested twice for it in the newborn screening and came back negative...but they feel since it's non-invasive just go for it! I love these doctors!!! Anyway, wish us luck and 
we should have the results in a day or two.
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