We found out on Wed that little Will does not have cystic fibrosis. In fact, he is not even a carrier. He had as much a chance of having the disease as not being a carrier for it (25%). It was a huge relief to find out that he will never have to think about CF in his life.
We discovered back in March or April that both Brig and I were CF carriers and that each child we had would have a 1 in 4 chance of having CF, and a 50% chance of being a carrier for the disease. We opted not to get an amnio to find out whether Will was sick, since there is nothing that can be done to treat it during gestation and the amnio does present a risk to the fetus. The worry over his possible medical condition was a dark cloud hanging over us the entire pregnancy. I thought that I would be able to handle whatever befell, but after Will was born, I knew that hypothetically dealing with that disease and actually watching your child struggle with it were two very different things, and that I would be devastated if he were sick. It has been a tremendous relief that all is well.
He has, however, failed both of the hearing tests administered on his right ear. I am not feeling too terribly concerned about this, though. The IUGR and the CF both turned out not to befall us, and I think out luck will continue to hold. Poor doctors probably have to be alarmists because of the legal profession (I am convinced that was the reason behind the IUGR diagnosis. Also, after concerns that my little boy will suffer a terrible and debilitating illness that would certainly take his life before he reached 40, and possibly much much younger, a hearing impairment in one ear really seems like no big deal. Nothing we couldn't handle.