Has anyone else developed SFN and POTS after the Covid Vaccine? My development was 5 months after vaccine. If so, have you received treatment and was it successful?
I don’t have either SFN or POTS - it seems that the injured draw from the same pool of symptoms and everybody has their own combination of symptoms.
If you want a little symptomatic relief of POTS, see these treatment guidelines on dysautonomia from European researchers. It’s not a cure, but the clinicians have been dealing with POTS for years and that is the best that they can do right now.
The Topics tagged healing-from-illness have some stories about how people have healed from chronic illness. So if you’re like me and you want to be ambitious and aim for a cure… that’s where I would look. The idea is to look back at history and try what worked for other people.
Thank you so much for this information. It is very helpful.