My daughter (7 1/2) has non-saltwasting CAH diagnosed 1 year ago. I also have a son (3) who does not have CAH. I am curious if any of you who had children diagnosed at birth and if so, did you undergo any prenatal treatment during subsequent pregnancies. I am pregnant now and am debating on whether to receive prenatal treatment or take my chances on whether this one will have CAH. My daughter has a mild form of CAH. I wonder if my next child has CAH, if it will be the same type of mild form non-saltwasting or could it be more severe. If anyone has any experience with this I would greatly appreciate the information. Thanks.