mooanne

230d

is there a specialist I should see for my Pots

Symptoms Involving Nervous & Musculoskeletal Systems

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  • raven2814

    230d

    Idk I'm trying find out

  • E11iefant

    230d

    They’re so hard to find!! I have Kaiser HMO insurance and there’s literally no one in the network😵‍💫

  • raven2814

    230d

    Oh

  • Sunshine_Sue

    230d

    Cardiologist is how I see. If you have a local hospital that recommends a Particular cardiologist that’s where I would go.

  • hazyeclipse

    229d

    Pots is a neurologic condition, or sometimes considered neurovascular, so ideally a neurologist or cardiologist

  • GuitarGal24

    221d

    A lot of cardiologist/ neurologists don’t know about it. It took me six years to get diagnosed. I finally got on a waitlist for the world expert located in Ohio and it was a year wait, I flew there and was finally diagnosed by him. His name is Dr. Blair Grubb and he has a Wikipedia. Even if you can’t go to him I recommend following his research. The best way to find doctors familiar with POTS is to join the Facebook group for dysautonomia international in your area and crowd source among the members. I found the rest of my local doctors that way.

☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision

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