Best way to get a POTS diagnosis?

Typically, neurologists and cardiologists or clinics specializing in dysautonomia will have the technology necessary to diagnose pots.

Then I had a table tilt test

Neurologist

I went to a cardiologist and he referred me to a dysautonomia specialist

A cardiologist/electrophysiologist is who diagnosed me. I’d seen a different cardiologist prior to that and his response was “you probably have some form of dysautonomia but it doesn’t matter which one so testing for it isn’t important”. So I found another doctor 🤷🏻‍♀️

I diagnosed myself with a pulse oximeter, and then went to a cardiologist and played dumb and he did a poor man's tilt in the office and he was like "have you ever heard of POTS"

i went to a neurologist who said i don’t have all the symptoms but that she still thought it was POTs, then sent me to every specialist under the sun to make sure it wasn’t something else. shes the one who treats my POTs as well.

I got admitted for tachycardia that they were relating to hypovolemia and dehydration. When it was fluid responsive and got worse with changing positions, i.e. laying to sitting and sitting to standing, they consulted cardiology. They did an echo due to family history of sudden cardiac death and cardiomyopathy. When it resulted as normal and my EKG was sinus tachycardia with borderline prolonged QT interval, they diagnosed me with POTS. I followed up with cardiology after discharge. They encouraged hyperhydration, increased sodium intake, and compression stockings. I have completed a 24 hour holter monitor and additional EKG’s. I am now also on a beta blocker, Propranolol,to help with continued tachycardia.

I went to my primary and then to a cardiologist. I also had a the poor man's table tilt done (sit down, measure blood pressure and then stand and measure blood pressure). I also see my cardiologist to keep a track of my heart via ultrasounds because of my EDS

Funny process; Went to my neurologist, who referred me to a cardiologist, who referred me to the geneticist. Had a DNA test done and surely enough they found POTS and hEDS in there. They only had me lay down and stand up a few times, so I was lucky to not have to do the tilt table test.

I went to my primary and she was able to diagnose me right then and there with a poor man’s tilt table test

I went to a cardiologist