LouLou! I love your lactivism!! <img src="i/expressions/heart.gif" border="0">
I had no prenatal testing done with either of my children. With my son, it was a surprize pregnancy and I knew that I wasn't going to not have him should any tests come back unfavorably, so I figured, why bother? He was sweat tested for CF after birth. At 8 I feel positive , despite not having any genetic testing, that he doesn't have CF. With our daughter, I wish that I would have had my husband genetically tested prior to her conception, which I am a little ashamed to say we didn't do - and now, especially after Lauren's experience, I see how you just can't be too sure - but we didn't, and as of yet she shows no symptoms of CF. I think at some point I will have her tested, but I am not ready to do that yet. with both children I did have ultra sounds and made sure that my tech looked for echogenic bowel - as that can be a sign of CF. Neither did, obviously.
I do think you need to ask yourself, is this invasive procedure what you need to have peace of mind, and what will you do if the results are not what you hope for?