Hi there,
I am new to this site. Our son is one week old and has been diagnosed with CF. He was admitted to the NICU when he was 2 days old with MI. He then had a rupture and had surgery. He is now starting to eat again yesterday, but still no stool. The nurses and doctors don't seem concerned, but I am scared to death that there is still somthing wrong. He has not started on enzymes, but will as his feeding amount increases. Has anyone else been through something like this?
I am new to this site. Our son is one week old and has been diagnosed with CF. He was admitted to the NICU when he was 2 days old with MI. He then had a rupture and had surgery. He is now starting to eat again yesterday, but still no stool. The nurses and doctors don't seem concerned, but I am scared to death that there is still somthing wrong. He has not started on enzymes, but will as his feeding amount increases. Has anyone else been through something like this?