My daughter Abby Michelle was just diagnosed today with CAH, and I'm in shock. She was just born on Saturday and now we learn she has this terrible disease. Our pediatrician has prescribed two drugs for her, I forget their names one is taken once a day the other is three times a day. I am completely baffled right now because I had such incredible dreams for my daughter and now she must deal with this disease for the rest of her life. Please if anyone can help me deal with this I would appreciate the help. I don't know what to do but cry. Why does this have to happen to our children.