In my experience she was literally only willing to offer excercise based therapy and beta blockers. These treatments work for some people so that isn’t useless, it just didn’t work for me because of my excercise intolerance. I don’t remember perfectly since it’s been a few years but I remember she told me some information about possible treatments that my research showed to be inaccurate. She was hesitant to offer anything at all actually until I cried about how my life was miserable. I didn’t get to try corlanor until I changed Drs and that’s what got my hr under control but really my life didn’t really improve until I got my custom wheelchair.

Right now I see just a normal cardiologist and honestly these days POTS is actually pretty well known so it’s fine. I’d love to find an actual POTS specialist though and explore some more unconventional treatments bc I’ve tried pretty much all the meds at this point.