Getting a Doctor to Listen: Tips for POTS Patients

Keep detailed notes of your symptoms; what you were doing before/after, what did you feel, how did they resolve, things like that. I have a few different conditions aswell, I've found the best thing is to basically "chart" on yourself and show them. Also helps if you are able to have someone with you at appointments to help advocate for you

I would actually recommend trying to get referred to a neurologist because it is an auto immune disorder, and it should be tracked by someone who can properly manage your immune system as well as show you how to properly maintain your body chemistry when it comes to water, salt, electrolytes… I’ve been to multiple cardiologists, and they have never wanted to take on POTS because they don’t see it as a ‘problem they handle’

Everything that’s already been mentioned but also make sure to include that the symptoms have been interfering with your life and functioning.