I can't help but share this and I'm not even sure it's related.  In the May Reader's Digest there is an article called "Saving Ryan".  This little boy has a rare disease called MPS I.  A crucial enzyme is missing that cells need to break down sugar.  Without it, cells become clogged, joints stiffen and organs are damaged.  Most kids don't live past their teens.  The family began a huge fundraiser and found a scientist, Emil Kakkis, P.h.D. biological chemistry and genetics, who eventually created the missing enzyme, and therefore a cure.  Could something like this be done with CAH?  I suppose if it could be someone would have done it.  At least our children have a medication that helps them live normal lives!  But Lynn, you are amazing how you continue to advocate for our kids!  Thanks, Pamela