hello! pots started after a really bad case of covid followed by mono. how are you treating this and does it ever getting fully cured?
Postural Orthostatic Tachycardia Syndrome (POTS)
I take fludrocortisone and atenolol medication wise. Electrolyte supplements are a tremendous help. I like Liquid IV. I drink as much water as I can (I know it’s hard though - especially if you have GI symptoms). I got IV fluids for about a year which was helpful, and I did physical therapy for awhile before my other conditions got too severe. I know some people experience a lessening of symptoms over time, but that hasn’t been the case for me. I have one friend who considers herself “cured” because she’s entirely symptom-free. Good luck!!
thank you very much! I am trying sacral cranial therapy. It is unbelievable. Praying its a cure.
What kind of physical therapy?
has this helped you a lot?
I am only upping my fluid intake and wearing compression socks for my symptoms at the moment but I am looking for other ideas as I have not gotten any better in two years now and honestly feels like it’s getting worse.
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