Hi Christina: This I believe is the best place to come. As you can see this is pretty close to a chat room. There are GREAT PEOPLE you will find here. I got more information here then my doctors office, other sites, books, ect. It gives you something a text book can't. It gives you REAL PEOPLE WITH REAL EXPERIENCES. As good as my doctor is, he still does not know what it is to have a child with CAH. I have a daughter that is 2 and a half and is a salt waster. Look at the "Ambiguious Genitalia" message on this page. That will give my story from the beggining. I prayed to find support and found it here on Christmas week. I felt tremendously alone until I found this page. Friends and family also can give great support, yet once again they don't know exactly how it is. And usually you spend more time trying to explain the disease then talking about your worries. Something you need to do. You will find most fo us venting, giving advice, and expressing our worries. I believe there is a true bond with all of us....we all love and care about our children VERY much. I got a piece of advice from a mom here that changed my life. It was the faith I didn't realize I lacked after the birth of my daughter. I can never repay that mom enough. If you need to e-mail me I am at (mack111@excite.com). You will truly find many friends and plenty of support here. GOD BLESS.