Hi Michele, I have two children, a boy and a girl with CAH non salt wasting. My daughter was treated at birth and is 8 years old. My son was diagnosed at 5 and is 14 now. He had done a substantial amount of growth in his 5 years. His bone age was that of an 11 year old. We have always been told that our son were be of short adult height. I am 5'3" and my husband is 5'10". We do not have very tall people on either side of the family. My son responded well to therapy and we were able to keep his bone age from advancing any further than 13 until he turned 13. Unfortunately, at 14 his bone age has advanced beyond again to 15. He is only 5'1". Apparently at a bone age of 15 you have reached 96% of your growth so the endo is predicting an end height of 5'4". I questioned my son's endos (he has had a few) about the introduction of growth hormone at some point in his treatment. They felt since he was doing so well with conventional treatment, it would not be necessary. There is always a concern about oversuppressing with meds which can also stunt growth. It can be awfully frustrating. We are seeing a growth specialist in a month to see if it would be advantageous for my son to take a growth hormone. However, at this late stage it may be ineffective. My son's endo sent me a clipping from a article with his blood tests results on Friday. In essence what the piece of the article concluded was that even if all things are perfect, treatment goes well, diagnosis is early, etc., CAH patients usually experience some loss of full height potential. In this article, the majority of patients fell into the 80-90% of their projected adult height. If you check some earlier posts on this board, there are a few posted by Mara, a delightful girl who gives her height as 5'6". I have never read a post where any CAH affected adult person has reached that height, they seem to always be below that. I would also love to know if there is anyone out there who did reach their projected height and how they did it!!!! Thanks.