← Return to Post Covid sweating: Is this common for others too?

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Have you been diagnosed with POTS?
There are specialist in autonomic nervous system who can help you with this.. POTS is a whole conversation 😊, but maybe it helps to know that I drink lots of fluid, including electrolyte solution. I take medication to control my heart rhythm (beta blockers and at one time Ivabradine, (medicine for heart failure) to allow for better blood flow throughout the body. I slowly rehabbed so my activity level is better.
Best,
Jen M RN

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Replies to "Have you been diagnosed with POTS? There are specialist in autonomic nervous system who can help..."

So sorry you are still struggling… it is awful. Sweating and all the post viral issues. Sending hope for better days.

I have found that propanolol helps me with stress as well. I also try and drink a lot of water. One of my symptoms of Long COVID is that if I drink ANYTHING other than water, I feel like I have a UTI. In 2023 I went to see a urologist, thinking I had a UTI, although my GP tested my urine and there was no bacteria. She said it sounded like interstitial cystitis. There was no evidence of that either, so I am sticking with water. I know it is the best thing to drink, but damn what I would give for some iced tea or a sprite.