I went to the endo last night for a regular checkup from him. Now he is not used to working with children, but he knows about CAH so I trust him when he says he knows whats going on. So last night we went and some of my levels were a little high and he couldn’t understand why. So he put me on 3 mg of Prednisone at night instead of 2 mg.  He is the kind of doctor who you have to ask questions about everything. And my mom was asking him what kind of CAH do I have? She had seen a lot of different types of CAH on here. So she asks him if I have Classical or Non-Classical? He said Classical. So she continued to ask him about whether I have saltwasting or not. He said saltwasting! Big surprise there!  Then she asks well is it mild or severe. He said severe. Now that was a surprise! We always thought I had a mild case of Non-saltwasting! Now  I would like to know a little more about SW CAH. Is it common for people that have SWCAH to sometimes go unnoticed like mine did? I have always had a hard time staying hydrated, but I always have water or very watered down tea. So is it common for people who have SWCAH to have a hard time staying hydrated?

Always ask your endo questions! I have learned that!