Newly Diagnosed via Newborn Screen - Help!

Hi all, We are new here as our daughter was just diagnosed at 8 days old via her newborn screen. We are a little overwhelmed and have some questions we hope the CF community or other parents might be able to help us with. Her mutations are G551D and D1152H, anyone else out there with that combination? We have been asked to collect a stool sample and take it to the lab for testing. Turns out, this has been nearly impossible as she is exclusively breast-fed and her stool is very watery and gets absorbed by her diaper. We have tried lining her diaper with Saran wrap but the stool just runs around it and gets absorbed by the diaper. Any other ideas? Second, we have been advised to supplement her diet with 1/8 tsp of salt. However; this is also nearly impossible as she is breast fed. I have tried administering small amounts to her in a syringe with water...she vomits it up. I have also tried pumping breast milk into a bottle and mixing in the salt. She takes it ok, but has since had a little nipple confusion. Frustrating! We're also new to the world of CPT. She cries. We cry. It's a disaster. Any advice on CPT in newborns? Any other newly diagnosed families out there going through what we're going through?
Source: Cystic Fibrosis Newly Diagnosed Forum - Category: Respiratory Medicine Authors: Tags: Newly Diagnosed Source Type: forums