Both carriers for Nonclassic CAH
Any carriers for nonclassic CAH? We did genetic testing and we are told we have a 25% chance of transferring this to a baby. We had genetic counseling. They said it’s the better of the CAH to have and can treat with medications, symptoms present in school age. I have been researching it. I found out my insurance covers 4 cycles of IVF a year and my doctor is finding out about the genetic probe if that is covered, which to my understanding selects to good DNA. I just don’t know if this disease is bad enough to need IVF to prevent? Should we just take our chances? I need advice. Even if insurance covers there would still be plenty of out of pocket that would probably be expensive. Better compared to no coverage but still. I also have low AMH level and my doctor says we shouldn’t wait much longer.