Ilyssa, You brought up some good points to keep in mind. Most of us if not all, as parents, want the VERY BEST for our children. If getting the very best means that we will ask the same questions over and over again than that is what we will do. Sometimes we know the answers and sometimes we dont. We are constantly looking for... hoping for that little shred of info that might help our child a little more. There are a lot of Endos in this world. Most of them do things differently. Some of them DO NOT KNOW ENOUGH about CAH. Those parents that have those Endos do not know that there is more to know until they find this site and then it is an outrageous eye opener. Sometimes we are passionate with our questions. Sometimes we are passionate with our answers. And sometimes we may even get carried away with our emotions. We deal with a condition that COULD mean the death of our child/children. That thought is always in the back of MY mind. Its not the same as "you could be hit by a car tomorrow" kind of thing. This is serious stuff. Everyday we give medicines that basically keep our children not just healthy but alive. I think we all know that there is no ONE person out there that has all the perfect answers on this. Dr New happens to be one of the people with the most experience. For that we respect her and her thoughts on the matter. Hopefully we can all take whatever info she throws at us... combine it with info we already have... and maybe, just MAYBE, make a better life for our children. Susan