I am pregnant with our second child and have a daughter with CAH.  We were in the process of getting genetic testing done and discussing with our insurance, when we found out I was pregnant.  We did a CVS and found out it is a boy, which deleted the need for Dex.  Since we still are not sure whether or not he has CAH, my question is about the process after he is born.  I assume we will treat him the same way we did our daughter until the test results are back - that is,  as if he does have CAH.  I have put a call into our doctors, but was wondering if anyone else has had any experience they might share about what they did, or what their doctors suggested.

Any input would be appreciated.