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Long COVID Severe → much better

Bedridden six weeks with long COVID, now much better on beta-blockers and antihistamines

Condition
Long COVID
At worst
Severe (mostly bedbound)
Ill before improving or writing
Not stated
Last post
Aug 2026
In their words
  • Condition: Long COVIDMade pre-existing POTS (and likely pre-existing MCAS) worse, so got diagnosed with LC. In context ↗
  • At worst: Severei went from being completely bedridden and struggling to write a 1-sentence text message for 6+ weeks In context ↗
  • Now: Much betterthings have improved for me immensely from when i first got covid. but i don’t think i’ll ever be how i was before. In context ↗
  • Began after: COVID03/31/2022 - contracted Covid (while having a POTS flare). In context ↗
Read from 17 of their posts and comments; links to the 10 this page draws on

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Summary

Tundra 48918 developed long COVID after a COVID infection on 31 March 2022 during a POTS flare and was completely bedridden for over six weeks. Beta-blockers and H1 antihistamines cleared most brain fog, and by spring 2024 they had completed a Master's, though they still get PEM. They do not expect full recovery.

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What they tried

Their words about each treatment
  • resting · Helpedi’ve slowly been getting better mostly via resting In context ↗
  • beta-blocker · Helped a lota beta-blocker + H1 antihistamine have all but eliminated my brain fog In context ↗
  • LiquidIV · Helpedsometimes my eye symptoms will improve just by eating or drinking water with LiquidIV In context ↗
  • Meloxicam · Not saidEnded up later taking Meloxicam (which my neurologist gave me for these inflammation migraines) and once I stopped this medication things have been fine since. In context ↗
  • psychiatric medication · Helped a lothave lived the last few years in virtual remission thanks to psychiatric medication In context ↗
  • Pfizer and Novavax COVID vaccines · Not saidalso the novavax vaccine In context ↗
  • Elara app · Helpedi HIGHLY recommend the app Elara. it's really excellent when i manage to keep up with it In context ↗
  • active rest · Helpedi think active rest has worked fine for me but i think i might be better overall (or get over PEM faster) if i did passive rest In context ↗

Approaches: H1 antihistamines · Beta-blockers · Pacing

Their path

Very severeSevereModerateMildNear normalRecoveredonset12 mo2 y3 y4 y

How ill they were on the ME/CFS severity scale, estimated from what they describe at each point, with time counted from when the illness began. Hover or tap a point. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
2022-03-31COVID infection during a POTS flare; bedridden for about six weeks03/31/2022 - contracted Covid (while having a POTS flare). In context ↗Severe
2022-09-21slowly improving with meds and rest; school wipes them outmy meds work pretty well and i’ve slowly been getting better mostly via resting. In context ↗Mild
2022-11-20beta-blocker plus H1 antihistamine all but eliminated brain fog; felt like old self 90% of the timea beta-blocker + H1 antihistamine have all but eliminated my brain fog In context ↗Near normalBeta-blockers (unspecified)
2024 springcompleted a Master's after being bedriddento completing my Masters this last spring In context ↗Mild
2026-08-08still paces and gets PEM; active rest works but passive rest might be betteractive rest has worked fine for me but i think i might be better overall (or get over PEM faster) if i did passive rest In context ↗Mild

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaisei think i might be better overall (or get over PEM faster) if i did passive rest In context ↗
  • Brain foga beta-blocker + H1 antihistamine have all but eliminated my brain fog In context ↗
  • Headaches & migraineMy first Pfizer shot gave me very weird migraines In context ↗
  • Gut problemsi feel less bloated In context ↗
  • Flu-like symptomspretty much just the ones under my jaw In context ↗

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