Polyglandular syndrome type II

I'm trying to connect with people who have PAS type II for information on diagnosis.

[MissGrey]

Hi there,

I haven't had a formal diagnosis of PAS II, but that's what my endo strongly suspected when I went for a consult - I'm looking for a new endo to get more detailed bloodwork so I can nail this down. I have tested positive for an unspecified autoimmune condition which is causing my adrenal to attack my thyroid (I'm on synthroid, armour, and hydrocortisone), and I tested positive for the markers of something like lupus or RA, but no lupus or RA present.

I've had morphea scleroderma for about a decade - I am hoping that's the cause of that mysterious positive marker.