Hi, this is my first post. My dd was diagnosed 2/08 with CF at the age of 11 years old. She had been losing weight for the past two years with increasing stomach pains. Since being diagnosed, she has been on enzymes for all her meals/snacks. We have her on a 2000 calorie a day - which she gets about 1500. She can't stand any of the shakes. She still complains of stomach pains even with adjusting her enzymes. She currently is in about the 2.5% - 3.0% for weight. She is so very, very thin. She has her 3 month appt on Thursday.
My question is on the g-tube. I have heard about it, but don't really have any information from people who have one or whose child has one. Do you think it was the right thing to do? Did it make a big difference? My dd is in 7th grade and really doesn't want to have it done for fear of being "different". She won't even eat snacks at school because no one else gets to do that, so she doesn't want to stand out.
Any thoughts or insights would be appreciated. Thanks
Stacy
My question is on the g-tube. I have heard about it, but don't really have any information from people who have one or whose child has one. Do you think it was the right thing to do? Did it make a big difference? My dd is in 7th grade and really doesn't want to have it done for fear of being "different". She won't even eat snacks at school because no one else gets to do that, so she doesn't want to stand out.
Any thoughts or insights would be appreciated. Thanks
Stacy