I understand the desire to downplay the seriousness of this desease; I do it sometimes, even now. Since my son is an "as if" I hold out that someday they will tell me it's not CF, that its something else that has a cure already, something that won't, possibly, shorten his life, or limit him in any way. But, as the one who is confronted every day with CF, I have had to be real about it. None of the things I hope for are likely to happen. The only someday I'll get is when his mutations are discovered. It won't change the fact that he has CF; it won't change his tx, or anything about his health or his life. Only those confronted with it 24/7 can truly understand what CF means; we have to let everyone else find their own acceptance. That's why this forum is so great. Sorry so rambling.