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Long COVID Severe → much betterIll 5.5 years before improving or writingNeeds ongoing treatment

Long COVID with palpitations and POTS much better on beta blocker and water/LMNT

Condition
Long COVID
At worst
Severe (mostly bedbound)
Ill before improving or writing
5.5 years
Last post
May 2026
In their words
  • Condition: Long COVIDIt’s just this week I’m starting to think it’s all COVID related. In context ↗
  • At worst: Severecouldnt get through a shower anymore In context ↗
  • Now: Much betterBut things are really improving again! In context ↗
  • Began after: COVIDIt’s just this week I’m starting to think it’s all COVID related. In context ↗
Read from 4 of their posts and comments; links to the 3 this page draws on

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Summary

A 29-year-old ill with long COVID from about 2021 still had palpitations, chest pain, tingling, numbness and muscle twitching two years later, with cardiomyopathy and later POTS. After a low point when they could not get through a shower, a beta blocker plus 100oz of water and LMNT daily reduced many symptoms; by May 2026 twitching was down to several a week.

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Asking aboutTide 11088’s story

What they tried

Their words about each treatment
  • beta blocker · HelpedI believe they are less because of the beta blocker im on due to the cardiomyopathy In context ↗
  • drinking 100oz of water a day along with 1 packet of LMNT · Helpeddrinking 100oz of water a day along with 1 packet of LMNT has reduced a lot of my symptoms In context ↗

Approaches: POTS medication

Their path

Very severeSevereModerateMildNear normalRecovered5.2 y5.4 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. The chart starts 5.2 years after onset: the story doesn’t say how ill they were before that. 1 step says too little to place on the scale and is only in the table. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
2021long COVID beganI feel like I’ve missed the last two years of my life and it’s heartbreaking. In context ↗Not stated
March 2026low point before POTS was diagnosed, too ill to showerI was feeling hopeless again, couldnt get through a shower anymore etc. In context ↗Severe
2026-05-13improving on POTS fluids, salt and a beta blockerBut things are really improving again! Unfortunately it has been a roller-coaster that I am still riding. In context ↗MildSalt, electrolytes and fluids

Adverse events

  • “Had another doctor find precancerous polyp in my intestines and after removal I went home and woke up bleeding a ton and almost bled to death needing a few transfusions” In context ↗ Other

Symptoms mentioned

Their words about their symptoms
  • Neuropathy & tinglingTingling and numbness, that’s going away, or a lot less often at least. In context ↗
  • Heart symptoms & palpitationsthe numbness and tingles usually came with severe heart palps and chest pain In context ↗
  • POTS & dysautonomiaI was also diagnosed with POTS In context ↗
  • Pain & fibromyalgiaMy thigh muscles were sore for a few days In context ↗
  • Anxiety & low moodI was feeling hopeless again In context ↗

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Asking aboutTide 11088’s story

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