Hello,
I found this group in hopes of some answers. My daughter was born
Dec.27,2006. Her heel stick test has screened a positive result for
one CF mutation. I have to have a sweat test done on her. As of now-
She is almost a month old and has no symptoms- She does not taste
salty, she has normal stools and she has gained two pounds and two
inches since birth. I guess I am just unsure of the chances of her not
having CF. There is NO history of it on either side, However my sister
is a carrier for it- so I suppose I am as well. I guess my question is
this- Is there any chance that she is just a carrier herself??