Miruvor
Sign up
ME/CFS Severe → near normalIll 11 years before improving or writing

Mostly bedridden and homebound with ME/CFS, now close to normal

Condition
ME/CFS
At worst
Severe (mostly bedbound)
Ill before improving or writing
11 years
Last post
May 2025
In their words
  • At worst: SevereI've been homebound and most days bedridden for a bit over 2 years. In context ↗
  • Now: Near normalI've been working full time for years now ... I wouldn't say my life is normal In context ↗
Read from 2 of their posts and comments; links to the 2 this page draws on

Request to remove this story

Summary

Owl 57078 fell ill around 2014 and spent the first two years mostly bedridden and homebound. They improved gradually: by 2017 they were back at work four days a week, sleeping at least 15 hours on days off, and by 2025 they had worked full time from home for years, walked almost daily and gone a long time without a full crash. They still pace carefully and expect flares.

Ask Miruvor AI

Asking aboutOwl 57078’s story

What they tried

Their words about each treatment
  • being very aware of the small signals my body gives me when I am overdoing it · HelpedHaven't had a real full on crash for a while as I've been very aware of the small signals my body gives me when I am overdoing it. In context ↗

Approaches: Pacing

Their path

Very severeSevereModerateMildNear normalRecoveredonset2 y4 y6 y8 y10 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
onsetIllness onset; homebound and mostly bedriddenMy first 2 years, I was mostly bedridden. In context ↗Severe
2017-06-24Back to work four days a week, no longer bedriddenI have seen a huge improvement though. I'm back to work 4 days a week In context ↗Mild
2025-05-22Working full time from home for years, daily short walks, no full crash for a whileI've been working full time for years now, but I work from home so I can take my naps during my breaks, I also take a short walk almost everyday In context ↗Near normal

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI know I will have huge flares again in the future In context ↗
  • Sleep problemsI can take my naps during my breaks In context ↗

Ask Miruvor AI

Asking aboutOwl 57078’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