My family has an appointment tomorrow for the Growth Hormone Study with Dr.New. My son has to sit and have his blood drawn over a two hour period of time and we have to take a class on giving him daily injections of his meds. Somewhere in there I will ask Dr. New that question because I also have a dilema with our DNA. For those of you who are wondering about whether or not Dr. New is coming on for a "Chat", I will say this - I have decided to try to ask her questions in person since some of the responses from this board were less than favorable. I don't want to alienate someone who I will be depending upon for my son's well being for the next 10 years. She has already said that she absolutely believes that there is no way a carrier can have the symptoms of a person with CAH. I will ask a couple more tomorrow if time permits and then I will report back. Thanks to you all for your patience.