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If youve had covid before, did you notice any worsening in your POTS after or did you stay the same? And are you hyperadenergic (high blood pressure subtype)?
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Generalized pain
Postural Orthostatic Tachycardia Syndrome (POTS)
Pneumonia
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818d
Covid didn't affect my pots. But months later now my hair us falling outš an acquaintance of mine said she got something called inappropriate sinus tachycardia from having covid but is seemingly getting better from it.
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My POTs developed after i had Mono about 5 years ago. i had COVID in july 2020 and my POTs got much worse
Bijoux_bean22 I also have gastroparesis and while I dont know yet long term I am currently sick and dont see a big different in symptoms, only it dramatizing my POTS and muscle/nerve pain. Though, worsening of POTS and MCAS can worsen Gi issues due to complications with symptoms. I believe I have omicron as if I had the other types i would not be okay. The last virus I got gave me pneumonia and POTS so Im suspecting now shits gonna get worse after recovering.
I am just getting out of isolation tomorrow. I know itās going to make the POTS and MCAS (Mast Cell Activation Syndrome) a nightmare but does anyone know how it can affect gastroparesis?
Yup, itās made my pots (and associated chronic fatigue) much worse unfortunately :/ Still not sure exactly how to improve it but going to physical therapy has been helping (especially with the fatigue part) a bit.
Covid is what started my POTS. Still going strong 6 months later :(
It got worse for 6 months. Then has slowly improved. I had i exactly 1 year ago today.
ā 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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