Noah came home today. He is stable.
I will explain more about the disease later. It sucks that he has it and its a lot of pressure to know that our little guy will need medication for life BUT as long as he is on it, he will be able to lead a normal life. I know you don't know what C.A.H. (Congenital Adrenal Hyperplasia) is and the consequences because its really rare but its not a good one to have. Details will follow later.
One thing I will say is that this has nothing to do with any previous "worries" the doctors had before. It is pure genetics. It is a rare gene that can affect the kids of two parents who are carriers. The pediatric endocrinologist was surprised that both Jeff and I have it considering our VERY different backgrounds, but unfortunately we have it and even more unfortunately its going to affect Noah his whole life. Hard not to feel guilty. =(