. I have the mutations finally!! Anyone know ANYTHING!?
wow -- I don't know. I guess I'd want to know what made them decide that the mutations are considered benign. Usually, from what I understood, they find a mutation and if they don't see it associated with clinical symptoms they call it benign. But if he has those symptoms, it may result in a reclassification of those mutations, since he DOES have mutations and he DOES have CF symptoms. That would seem to be the whole determination of diagnosis -- but I'm not a doctor, so who knows if I am right.