My son's 40 mutation panel went out last week - a week ago today. I still have heard nothing and I am starting to over obsess. My pedi has assured me from day one that he will NOT have CF - he is too big - too low sweats etc etc. He ordered the panel so he will have to tell me if he has a mutation or a diagnosis. I am confident that I may say something along the lines of "well I guess YOU were wrong eh?!" if he does have even one mutation from that panel. Or would I just be speechless and not care that he was wrong? At this point I just want answers for my son, it has been a long road to them!
What were your reactions at diagnosis if you don't mind sharing?
What were your reactions at diagnosis if you don't mind sharing?