Miruvor
Sign up
ME/CFS Severe → somewhat better

Unable to speak for years with ME/CFS, now somewhat better with rest and pacing

Condition
ME/CFS
At worst
Severe (mostly bedbound)
Ill before improving or writing
Not stated
Last post
Oct 2026
In their words
  • At worst: SevereI didn’t speak for a few years and now I can chat for about ten minutes a day In context ↗
  • Now: Somewhat betterWith rest and pacing I have improved my talk time . In context ↗
Read from 4 of their posts and comments; links to the 4 this page draws on

Request to remove this story

Summary

A Reddit user with ME/CFS who did not speak for a few years and now manages about ten minutes of chatting a day, mostly texting. They credit rest and pacing with improving their talk time and say gentle swimming is the exercise that suits them best. Years of following a specialist's advice to do 25% more than they thought they could cost them their twenties, and a freezing outdoor pool left them collapsed and half carried to the car.

Ask Miruvor AI

Asking aboutShore 81298’s story

What they tried

Their words about each treatment
  • freezing outdoor pool · WorseTotal disaster - straight in and out then collapsed and had to be half carried to the car. In context ↗
  • rest and pacing · HelpedWith rest and pacing I have improved my talk time In context ↗
  • gentle swimming · HelpedThis is why gentle swimming is best exercise for me as you don’t have to talk In context ↗
  • Zolmitriptan · HelpedZolmitriptan 👏🏻👏🏻👏🏻 In context ↗
  • as much as you think you can and then 25 percent more · Much worseDutifully did that for years and lost my twenties 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. 1 step says too little to place on the scale and is only in the table. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
—ME/CFS onsetYes I didn’t speak for a few years In context ↗Not stated
—unable to speak for a few yearsYes I didn’t speak for a few years and now I can chat for about ten minutes a day In context ↗Severe
2026-10-22talk time improved with rest and pacing; mostly textsWith rest and pacing I have improved my talk time . In context ↗ModeratePacing and the energy envelope

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Headaches & migraineZolmitriptan 👏🏻👏🏻👏🏻 In context ↗

Ask Miruvor AI

Asking aboutShore 81298’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