Hi!  I just gave birth to a daughter with CAH.  She has the salt wasting form and is severely virilized.  She is facing surgery at six months of age.  We live in Connecticut, our Endoc. Dr. is Dr. Genel at Yale New Haven Hospital.  We are looking to hear from parents that have dealt with this in their children, how they have handled it and if surgery, what was the outcome.  Any information and words of support would be appreciated.  Thanks so much.  By the way, I notice in my 5 week old body odor.  Anyone else experience this?