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Long COVID Mild → no benefitIll for 6 years

Long COVID with orthostatic intolerance, no better after gym or breathing training

Condition
Long COVID
At worst
Mild (working or studying, with limits)
Ill for
6 years
Last post
Feb 2026
In their words
  • Condition: Long COVIDOrthostatic Intolerance is a big issue for me a long hauler. In context ↗
  • At worst: MildI have since stopped working, and decided to focus full-time on trying to, not only stop exacerbating it, but also reversing it. In context ↗
  • Now: No benefitMy issue has been progressive ... I haven't had much success. My chest muscles seem permanently screwed up. In context ↗
  • Began after: COVIDOrthostatic Intolerance is a big issue for me a long hauler. In context ↗
Read from 2 of their posts and comments; links to the 2 this page draws on

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Summary

A long COVID patient ill since 2020, with orthostatic intolerance they said was worsened badly by dehydration and progressive chest and upper back tightness they blamed on poor pacing. They stopped working to focus full time on stopping and reversing the muscle wasting. Almost daily gym work and inspiratory muscle training had not helped, and they feared the damage was permanent.

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What they tried

Their words about each treatment
  • ORS formula · HelpedBefore anyone says anything about glucose, I can tell you 100% it makes the total difference when it comes to hydration. In context ↗
  • keto diet · WorseIn the last I tried the keto diet with just using pure electrolytes and water, and it was really hard keeping up. I could feel the difference. It was awful. In context ↗
  • backpod · Not saidthere's maybe 70% chance I tried (backpod, LDN, apheresis, massage, lacrosse ball, supplements, countless drugs, physiotherapy, etc. ) In context ↗
  • going to the gym · No changeI go to the gym almost everyday, without making it worse, and try to work on these muscles. In context ↗
  • inspiratory muscle training · No changeI also do plenty of inspiratory muscle training, to try and expand the ribcage. It's really not moving the needle. In context ↗

Their path

Very severeSevereModerateMildNear normalRecoveredonset12 mo2 y3 y4 y5 y6 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 were
2020long COVID began; upper back and chest tightness startedLong-term chest muscle damage (since 2020). Upper back super tight. In context ↗Mild
2026-02-02chest/back tightness progressed; stopped working, muscles atrophiedI have since stopped working, and decided to focus full-time on trying to, not only stop exacerbating it, but also reversing it. In context ↗Mild

Adverse events

  • Keto and low-carb diets“In the last I tried the keto diet with just using pure electrolytes and water, and it was really hard keeping up. I could feel the difference. It was awful.” In context ↗ Made symptoms worse

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseeven talking was a trigger, and I was not aware at first In context ↗
  • POTS & dysautonomiaOrthostatic Intolerance is a big issue for me a long hauler. In context ↗
  • Pain & fibromyalgiaLong-term chest muscle damage (since 2020). Upper back super tight. In context ↗
  • Muscle weaknessMy muscles at my chest and back area seem atrophied and even scarred. In context ↗

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