I'm a dad with one child with cf. We all take turns with sharing time during vest treatments and that is good. I have never missed a clinic visit because I think it is important for dad to be there as well. Much of my time is spent reading and learning more about cf. I don't post very often but if you look at whose logged in here, I'm here alot. My wife is not really interested in the web info of this disease but she does play an important part as well. I would like to say to the dad's out there, our kid's really need us!