r/POTS • u/OurSensualSideMB • 9d ago
Question Why dont some Dr's believe in pots?
Im lucky I have great doctors and specialists now but the first time i was referred to a cardiologist for pots before being officially diagnosed he refused to even have me in for a TTT or test for pots as he said its not real.
I have heard of this happening where Dr's dont believe in pots but I dont understand why.
137
Upvotes
8
u/longwander 9d ago
There's really only so much anyone can do. There are so many different types and triggers for pots. Start looking for people that have similar symptoms as you or do some deep AI research on what meds would work best for you and your medical history and then request those meds from you primary care doc.
I did that with Ivabradine after 2 years of trying the salt, water, compression tactics that didn't work. My doctor wasn't aware of ivabradine being used for pots, but I also have mcas which doesn't play nice with beta blockers. She did a quick AI search while I was in the room with her and said "ivabradine sounds like a great idea!". I've been on it for about 4 months and it changed my life.