Hi everyone! I'm a little confused with the diagnosis (or lack of) in my two sons. They both have had positive sweat tests, (76 and 89), and have the delta F508 mutation. The doctor only ran the test for the more common mutations, so they only found the one. He has ordered the full test, but told us it could be up to two months for the results to come in. Anyway, they are both pancreatic sufficient, and aren't presenting with too many other symptoms (just nasal polyps in the older one, and pretty much nothing in the younger one) The doc sent us home, and told us they would call us if they found a second mutation. Is it wise to just let it go? Any advice would be appreciated! Thanks!<img src="i/expressions/face-icon-small-smile.gif" border="0">
Carrie
Carrie