jenandcorey
New member
My husband's sister has CF, so when we were trying to conceive, we had genetic testing done. He has one mutation (not sure which one), and I don't have any. I know there is a possibility that the carrier gene has been passed on to our son. How important is it to have him tested as a child? He's almost 4 years old. I know this will be an important issue when he's of child bearing age, but what about now? Any reason to find out?