Hello everyone,

I'd like to know if any of you have had gene testing along with blood
tests for your 3Beta HSD dianosis or if your doctor diagnosed it
strictly from blood tests.

If, for any reason, I ask questions and you don't have the answer,
please let me know, or let me know that you'd rather not answer, but
I'm trying to get a better handle on our diagnosis and symptoms. I
haven't contacted the doctor I know at NIH yet because I'm still trying
to figure out what angle I could present to him so that we could get him
to acknowledge that it's worth a study IYKWIM.


A couple of people still hasn't filled out the questionaire for the
group. It would be very helpful if we had more answers and it's
anonymous (which means no one will know your answers specifically, but
it will show a group consensus. There's a link somewhere in this e-mail
where you can click to take the survey. If you have problems finding
it, please let me know.

Thank you.