I was curious whether anyone else has this in addition to PCOS? I thought when I was diagnosed with POTS that it had been caused by my Lyme disease (however I went through very intense Lyme disease treatment for 2-3 years since I was undiagnosed for over 10years with Lyme and I seemed to recover from most symptoms after treatment..) I finished treatment for it about 2 years ago. but I am still experiencing tons of dizziness/feeling like I’m going to faint recently and it feels like my POTS… read more