We saw the pulmonologist today. He said with Cate's low sweat test (18), and lack of mutations on her newborn screen and mutation panel that he would be completely shocked if she had CF. He said he didn't think she had CF at all. Instead, he said her history and chest x-ray looked like asthma. I asked him about her poor weight gain, and he really couldn't explain it. He said the two episodes of rectal prolapse were probably a combination of her bad constipation and her anteriorly displaced anus. He is an expert on CF, so I trust him. He is putting her on daily inhaled steroids, a short course of oral steroids, and albuterol. It's worth a shot. I mean, I'm sure all of you would prefer to have asthma over CF. He said he'd see us back in 3 months. If it is asthma, we will see improvement. If it's something else (CF maybe), then we'll do more testing then. I really want to believe him. But, my husband and I both want to know for sure, so we're going to ask our pediatrician to do the Ambry Amplified Test anyway. I'll have to let you know what turns out. As for now, pray that she does have asthma and that these meds will work. (Never thought I'd be praying for my child to asthma!)