Miruvor
Sign up
ME/CFS Moderate → much better

Housebound and partly bedbound with ME/CFS, now mild-moderate after pacing

Condition
ME/CFS
At worst
Moderate (mostly housebound)
Ill before improving or writing
Not stated
Last post
Jun 2026
In their words
  • Condition: ME/CFSassume that I have ME/CFS and try pacing In context ↗
  • At worst: ModerateI went from pretty solidly moderate to mild (when I'm not in a crash) In context ↗
  • Now: Much betterI went from pretty solidly moderate to mild (when I'm not in a crash), and my crashes now are a lot easier to manage In context ↗
Read from 2 of their posts and comments; links to the 2 this page draws on

Request to remove this story

Summary

Island 24504, 21 and non-binary, was housebound apart from college classes and partly bedbound, at a moderate level. Pacing helped a lot over about a year, and they improved to mild-moderate, able to shop with someone, take short walks, cook simple meals and go to a bar without a big next-day crash. They still had crashes and were awaiting an official diagnosis.

Ask Miruvor AI

Asking aboutIsland 24504’s story

What they tried

Their words about each treatment
  • pacing · Helped a lotLuckily for me, pacing helps a ton! ... I was able to go from housebound (minus attending college classes) and partially bedbound to being able to go grocery shopping with someone!! In context ↗
  • compression materials and electrolytes · Not saidI'm planning on needing lots of lay down time and compression materials for blood pooling in my legs. ... I'm also bringing more electrolytes than I usually go through. In context ↗

Approaches: Pacing

Their path

Very severeSevereModerateMildNear normalRecovered

How ill they were on the ME/CFS severity scale, estimated from what they describe at each point, in the order they describe; they don’t give enough times to place each step. Hover or tap a point. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
—housebound apart from college classes and partly bedboundI was able to go from housebound (minus attending college classes) and partially bedbound In context ↗Moderate
over about a yearpacing helped; moved from moderate to mild-moderatepacing helps a ton! ... I went from pretty solidly moderate to mild In context ↗MildPacing and the energy envelope
2026-06-02still mild when not crashing; crashes easier to managemy crashes now are a lot easier to manage and maintain than it was last year In context ↗MildPacing and the energy envelope

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaisemy crashes now are a lot easier to manage and maintain than it was last year In context ↗
  • POTS & dysautonomiacompression materials for blood pooling in my legs In context ↗

Ask Miruvor AI

Asking aboutIsland 24504’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