It’s nice to know there’s someone else out there with POTS that got worse after COVID…though I’m sorry that had to happen.

That happened to me too, and I wondered if I was imagining it or had fallen behind on the self-care measures I was doing. My care team diagnosed me with long COVID as well. At first they said, “These increases in symptoms are usually transient in nature,” until of course they weren’t. Wishing you all the best.