Chaya, First of all, CAH is a very treatable disorder. Most of us that partisipate on this board had never heard of CAH before our child was diagnosed. This is a very good place for support, to get questions answered and to find out what you should be taking with your daughter's doctors about. A very good explaination of CAH can be found on the Johns Hopkins web page http://www.med.jhu.edu/pedendo/cah/index.html This gives a good, general explaination that most of us non-scientific types can understand. If your daughter has CAH, then she will need medication (probably Cortef) 3 times a day, on time. She will need to visit her pediatric endocrinologist about every 3 months for a check up and blood-draw. She will need to wear a MedicAlert bracelete, because she will be steroid dependent. You will also need to learn how to give her an inter-muscular injection, for very serious situations. Right now what you need to do for your daughter is to work with her pediatrician to get a referral to a pediatric endocrinologist so she can be checked. There is a very simple blood test (ACTH test) that will tell the doctor if your daughter does or does not have CAH. When you first hear about CAH, it is scary. I cried for two weeks. But now, 5 months later, it is no big deal. I just make sure my daughter gets her medication on time and that we ALWAYS have her medicines with us. Where ever Olivia is you will find her medicine kit. Good luck!