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SarahProcter
Guest
My daughter's sweat test at 2 months old was 41. I asked the doctor whether he would have concluded that she did NOT have CF if it had been 39. He said no, that for infants, he finds anything above 30 "highly suspicious" and would have continued to investigate. We did end up finding two mutations, conclusively confirming her diagnosis, when they did the full genetic sequence instead of just the screen. So, everything I've heard supports your gut feel that you should push for full genetic testing, especially in light of the weight gain issues and poop issues you've faced.
Did they do a fecal elastase test to check for pancreatic (in)sufficiency?
Did they do a fecal elastase test to check for pancreatic (in)sufficiency?