Miruvor
Sign up
Long COVID Severe → much betterIll 2.5 years before improving or writingNeeds ongoing treatment

Mostly in bed for months with long COVID, much better and back at work after pacing

Condition
Long COVID
At worst
Severe (mostly bedbound)
Ill before improving or writing
2.5 years
Last post
Nov 2024
In their words
  • Condition: Long COVIDI got Covid last July and ended up off work for 6 months, as I ended up with Long Covid. In context ↗
  • At worst: SevereI spent months where I was mostly in bed. In context ↗
  • Now: Much betterI'm nowhere near as bad as I was now and I'm back at work. In context ↗
  • Began after: COVIDI got Covid last July and ended up off work for 6 months In context ↗
Read from 12 of their posts and comments; links to the 8 this page draws on

Request to remove this story

Summary

After catching COVID in July 2022 they were mostly in bed for months and off work for six months with long COVID: fatigue, brain fog, muscle pain and crashes. The best help they got was pacing explained by an occupational health doctor, and they credited that advice. They returned to work, but were still exhausted much of the time, needing naps and staying near their limit. Over two years on they were still limited at their last post.

Ask Miruvor AI

Asking aboutGrove 72956’s story

What they tried

What they credit

Also tried

painkillers· No change
Their words about each treatment
  • pacing · HelpedThis is exactly how pacing was explained to me ... I would say it's really helpful In context ↗
  • painkillers · No changepainkillers have had little to no effect In context ↗

Approaches: Pacing

Their path

Very severeSevereModerateMildNear normalRecoveredonset6 mo12 mo18 mo2 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
July 2022Caught COVID, developed long COVID, mostly in bed and off workI got Covid last July and ended up off work for 6 months In context ↗Severe
2023-05Considerable progress and back at work, still fatiguedI've made considerable progress since last year but still suffer with fatigue In context ↗MildPacing and the energy envelope
2023-08Crashed after a week's holiday with challenging walksafter the holiday, it's eventually caught up In context ↗Mild
2024-11-08Over two years in, back at work but still fatigued, foggy and in muscle painI'm over two years in of having Long Covid and the main symptoms are Fatigue, brain fog and muscle pains In context ↗Mild

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI go slightly over and crash In context ↗
  • Brain fogwhen it kicks in, it becomes difficult to carry out simple tasks In context ↗
  • Pain & fibromyalgiathe main symptoms are Fatigue, brain fog and muscle pains, wjivh is mainly in my legs In context ↗
  • Muscle weaknessMy body would also become weak at the same time as the brain fog started. In context ↗
  • Sleep problemsI've had to sleep twice today and will probably have messed up tonight's sleep due to that In context ↗

Ask Miruvor AI

Asking aboutGrove 72956’s story

Similar stories

  • Unable to walk around house with long COVID, much better after pacing and antihistamines

    Much better Falcon 84129 Long COVID Severe at worstIll 3 years before improving or writing reddit.com Oct 2026

    A Canadian man with long COVID for about three years was unable to walk around the house for the first two years, with constant migraines, brain fog and PEM. From year three, pacing, rest, stress reduction, H1/H2 antihistamines, hydroxyzine for sleep,…

  • Mostly bedbound and housebound with ME/CFS, pacing and rest helped before a relapse

    Relapsed Valley 16092 ME/CFS Moderate at worstIll 25 years before improving or writing reddit.com Oct 2026

    Valley 16092 has had ME/CFS and fibromyalgia for about 25 years; stress and lifelong health problems led to a crash from 60-hour workweeks. They never became severe but have been mostly bedbound and housebound, and pacing, rest and comorbidity medication…

  • Mostly housebound with ME/CFS, now a little better on Klonopin and low-dose naltrexone

    Somewhat better Valley 89571 ME/CFS Moderate at worstIll 3 years before improving or writing reddit.com Oct 2026

    Joseph, 47, in Los Angeles, developed ME/CFS in January 2024, about 18 days after a second COVID infection. He declined from mild to the bad end of moderate over six months, becoming mostly housebound. Klonopin, low-dose naltrexone, midodrine and propranolol…

  • Long COVID brain fog, somewhat better with nicotine patch and naltrexone

    Somewhat better Pebble 25278 Long COVID Mild at worst reddit.com Oct 2026

    Pebble 25278 developed long COVID with brain fog, distorted smell, headaches, nerve pain and trouble sleeping. A quarter of a 10 mg nicotine patch restored much of their speech and thinking, and low-dose naltrexone further raised their cognitive and physical…

A little hope, every Sunday

New recovery stories and data-driven research on ME/CFS and long COVID. Ideas worth considering, and the evidence behind them.

Free · Unsubscribe anytime