Hey there - me AGAIN!

I am feeling a bit overwhelmed and stupid about this whole CAH thing and am SO THANKFUL for all your info.  It has been a tough couple weeks and feel a bit desperate for answers.  If there are other places y’all recommend I look, read, etc. I would love to hear them!

As for getting to NIH, how do I go about doing that?  Also, I am confused as to the results of genetic testing.  Will my son’s test tell me if I should pursue my own ACTH, etc. or I am seperate all together as far as my own diagnosis?  You said that I would also get genetic testing there for free.  Does that mean I, too, would need to have a genetic test done at some point?  Do I ask a Dr to pursue this or am I just being a hypocondriac in advance of any genetic evidence from my son’s test?