I hope you don't mind if I jump in here and ask a question. Me and my husband found out we are both carriers for CF. I have a mild mutation (not sure of the actual mutation) I believe is what they said however my husband has a rare mutation that there isn't much info on. I have seen a genetic counselor and spoke regarding the options. I am 8 weeks pregnant and patiently waiting to get a CVS test to determine if the baby has CF or is just a carrier. I actually have 2 questions.. First to the woman who found out during pregnancy that they and their husbands were carriers. Did you experience anything abnormal while pregnant or with the babies growth? Also, my husband and I did IUI with sperm wash and wondered if washing the sperm can decrease our chances of the baby having CF by taking only my husbands healthy sperm and eliminating and bad forming or not as good sperm. I actually asked that to the genetic counselor and she said they have not really studied it but it is a possibility and a very good question. I am so nervous about the future of this pregnancy. It took me years just to get pregnant now I am faced with this. Any help would be greatly appreciated.