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Long COVID Severe → no benefit

Bedridden for months with long COVID and suspected POTS, still palpitations on metoprolol

Condition
Long COVID
At worst
Severe (mostly bedbound)
Ill for
months
Last post
Feb 2024
In their words
  • Condition: Long COVIDhttps://www.reddit.com/r/covidlonghaulers/comments/1ah81rl/_/kp5jlnk/ In context ↗
  • At worst: SevereI’ve been bed ridden for months now In context ↗
  • Now: No benefitI’ve been bed ridden for months now In context ↗
Read from 1 of their posts and comments; links to the one this page draws on

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Summary

A Reddit user in r/covidlonghaulers reported being bedridden for months and suspected POTS, with doctors finding nothing seriously wrong. Palpitations usually came on with physical exertion such as work or bowling league, though they hadn't done those in weeks. They took 25 mg metoprolol extended release, which lowered their heart rate and blood pressure; they still sometimes felt palpitations at night and had felt two shortly before posting. They had been afraid to start it.

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What they tried

Their words about each treatment
  • metoprolol extended release · Helpedthey have brought my heart rate down and blood pressure In context ↗

Symptoms mentioned

Their words about their symptoms
  • Heart symptoms & palpitationsmine usually happen when I work (blue collar) or after I bowl league something physically exerting In context ↗
  • POTS & dysautonomiathe doctors don’t think anything is seriously wrong with me besides possibly having pots In context ↗

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