I try to absorb all about CAH in any form that is posted on here like a sponge! I want to know everything from the good to the bad.  From the adults with experience to the newborn. 

When I got my grandson 7 yrs ago who has SWCAH I had no one but the internet, endo and my family which still does not have a clue about CAH except for my immediate family that is. 

Look what I have now. This message board, Cares Foundation and the most fabulous book!!  KNOWLEDGE 1st hand from someone that has experienced it. That is everything.

I don’t think anyone is ever arguing. We are stated what we feel and think and know and experience. 

Aimee I wish I could express myself like you do. I’m not very good with words. It’s like I can never say in words what I exactly mean SEE lol. 

Jenny