POTS/VM mcas
Hey all,
I got VM/POTS after covid. Has anyone tried flordricortisone or cromlin/ketotifin for their symptoms? I react to every med I’ve been prescribed and I have severe GI issues. I’m always on a boat feeling and on the verge of passing out. I have blacked out before. They told me to wear compression socks and drink more salt but I feel like there has to be more to it. Anyone else? I
u/heyu179 — 4 days ago