COVID and POTS: Did it Worsen Your Symptoms?

Covid didn't affect my pots. But months later now my hair us falling out🙄 an acquaintance of mine said she got something called inappropriate sinus tachycardia from having covid but is seemingly getting better from it.

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 it’s going to make the POTS and MCAS (Mast Cell Activation Syndrome) a nightmare but does anyone know how it can affect gastroparesis?

Yup, it’s 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.