What’s the quickest way to a POTS diagnosis? I’ve been diagnosed with MCAS, hEDS, and suspected POTS, all for at least a few years. My POTS symptoms are worsening and I need to seek treatment for this. But I switched my insurance so I’ll need a referral from my PCP no matter what. What should I ask for to accelerate the process?
Postural Orthostatic Tachycardia Syndrome (POTS)
Mast cell activation syndrome
Ehlers-Danlos Syndrome (EDS)
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