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ME/CFS Moderate → no benefitIll for 2 years

ME/CFS fatigue for two years, stopped them working, still no improvement

Condition
ME/CFS
At worst
Moderate (mostly housebound)
Ill for
2 years
Last post
Jul 2026
In their words
  • Condition: ME/CFSI eventually recovered but then what feels exactly like CFS started about 6 months later In context ↗
  • At worst: ModerateIt's so severe I can't work and can barely function at home some days In context ↗
  • Now: No benefitthis chronic fatigue started one day and never left In context ↗
  • Began after: COVIDeven though I recovered from long covid, I still had enough damage done to my body that putting alcohol into it everyday for 6 months completely screwed me up again but in a different way
Read from 6 of their posts and comments; links to the 4 this page draws on

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Summary

Birch 82096 had long COVID twice, for 8 and then 18 months, with respiratory, POTS, heart and immune symptoms, recovering fully both times. After heavy daily drinking began, chronic fatigue started within six months; it has lasted two years, eventually stopping them working. Progesterone cream was the only thing that helped the long COVID symptoms. They quit drinking a few weeks before writing, hoping to recover.

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What they tried

Their words about each treatment
  • prescription amphetamines · WorseInstead of giving me the energy they used to give me they just speed up my mind- not my physical energy. In context ↗
  • progesterone cream · HelpedThe only thing that ever helped my long covid symptoms was progesterone cream. In context ↗
  • quitting alcohol · Not saidFinally quit drinking a few weeks ago and I'm praying that months without alcohol my body will recover. In context ↗

Their path

Very severeSevereModerateMildNear normalRecovered12 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. The chart starts 8 months after onset: the story doesn’t say how ill they were before that. 2 steps say too little to place on the scale and are only in the table. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they were
onsetFirst long COVID infectionFirst time I had it was for 8 months then got better and completely recovered. In context ↗Not stated
8 moRecovered from first long COVIDthen got better and completely recovered In context ↗Recovered
20 moSecond long COVID infectionLess than a year later I got it again and it lasted for 18 months. In context ↗Not stated
3.2 ySecond long COVID stopped; full recoveryThen it just stopped and I completely recovered. In context ↗Recovered
4 yChronic fatigue began after months of heavy daily drinkingI started drinking alcohol heavily like everyday and in less than 6 months this chronic fatigue started one day and never left. In context ↗Mild
5.8 yWorsened until unable to workIt's so severe I can't work and can barely function at home some days In context ↗Moderate
2026-07Quit drinking a few weeks earlier, hoping the fatigue will liftFinally quit drinking a few weeks ago and I'm praying that months without alcohol my body will recover. In context ↗Moderate

Adverse events

Symptoms mentioned

Their words about their symptoms
  • POTS & dysautonomiaLong covid had tons of symptoms for me not just respiratory but pots symptoms In context ↗
  • Breathlessnessnot just respiratory but pots symptoms and horrible immune system symptoms In context ↗
  • Heart symptoms & palpitationsI had multiple symptoms an addition to that like respiratory, heart, nervous system etc. In context ↗
  • Flu-like symptomsMy immune system flares were horrible like my body was fighting an illness In context ↗

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