I don't think the doctors have a clue what to do with me. No clotting tests as far as I know. I will look at APS information. I really think I may have POTS instead of SVT. The electrophysiology cardiologist just wants to throw drugs at me instead of doing any testing. Ugh

I still have a Gastroenterology appt to go to for further evaluation of my dysphagia. The Allergist thinks I have some kind of Mast cell disorder. Further evaluation is needed for that.

Annie, what do you think about the new Thymectomy study?

Thanks for listening. This disease is exhausting.
Sandy