Covid
Sighs, this stinks. My first known infection, I also had to take care of myself. It was so rough and scary. I hope you're able to get lots of rest!
More on reddit.comPOTS has doubled since the pandemic
Covid can also worsen existing dysautonomia. I have had POTS since I was a child (I have hEDS so I was born this way lol), and my covid infection from earlier this year has made my symptoms much worse. Vaccinated and everything, and I still got it 😭
More on reddit.comSo If It’s Dysautonomia, Wouldn’t Long Covid Be Permanent?
I believe primary dysautonomia doesn't exist outside actual observable nerve damage, and it's always secondary to something, and when they can't find the underlying cause it's because the current medical field just doesn't have the tools, like they don't have the tools to understand what's happening to us, or cfs, or a bunch of other conditions, probably something autoimmune but we won't know for sure for sometime.
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