Miruvor
Sign up
ME/CFS Moderate → somewhat betterIll 5 years before improving or writing

Moderate ME/CFS, somewhat better over five years while resting at home

Condition
ME/CFS
At worst
Moderate (mostly housebound)
Ill before improving or writing
5 years
Last post
Aug 2025
In their words
  • Condition: ME/CFSI was diagnosed with cfs at 14yo, right in the height of covid In context ↗
  • At worst: Moderategoing from moderate to more mild over the last 5 years In context ↗
  • Now: Somewhat bettergoing from moderate to more mild over the last 5 years In context ↗
Read from 1 of their posts and comments; links to the one this page draws on

Request to remove this story

Summary

Trail 37781 was diagnosed with ME/CFS at 14, during the COVID pandemic, and improved from moderate to mild over five years while resting at home. In August 2025, aged 19, they tried a four-hour hotel breakfast trial shift, managed three hours, and crashed, sleeping six hours and still feeling foggy, exhausted and achy. They were left unsure how work could fit within their limits.

Ask Miruvor AI

Asking aboutTrail 37781’s story

What they tried

Also tried

part-time work (hotel breakfast trial shift)· Worse
Their words about each treatment
  • rest at home · HelpedThankfully with covid I could rest a lot at home and focus on getting better, going from moderate to more mild over the last 5 years In context ↗
  • part-time work (hotel breakfast trial shift) · Worsethe shift was only 4 hours and I only made it through 3 before pushing myself too hard and sleeping for 6 hours when I got home In context ↗

Approaches: Radical rest

Their path

Very severeSevereModerateMildNear normalRecoveredonset12 mo2 y3 y4 y5 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
2020, age 14diagnosed with CFS at 14 during the COVID pandemicI was diagnosed with cfs at 14yo, right in the height of covid In context ↗Moderate
2025gradual improvement from moderate to mild over five years with lots of rest at homeThankfully with covid I could rest a lot at home and focus on getting better, going from moderate to more mild over the last 5 years In context ↗Mild
2025-08-21crashed after 3 hours of a 4-hour hotel breakfast trial shiftthe shift was only 4 hours and I only made it through 3 before pushing myself too hard and sleeping for 6 hours when I got home In context ↗Mild

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI only made it through 3 before pushing myself too hard and sleeping for 6 hours when I got home In context ↗
  • Brain fogI still feel foggy, exhausted, and achy In context ↗

Ask Miruvor AI

Asking aboutTrail 37781’s story

Similar stories

  • Almost bedridden with ME/CFS, now much better after a specialist regimen and pacing

    Much better Fox 20038 ME/CFS Severe at worstIll 6.5 years before improving or writing reddit.com Oct 2026

    A California woman infected with COVID in March 2020 was sick six months, partly recovered, then relapsed and was almost bedridden by early 2023, unable to drive and sensitive to light and noise. An out-of-pocket ME/CFS specialist regimen of LDN, Abilify,…

  • Unable to walk with long COVID, much better on immunosuppressants and anti-inflammatories

    Much better Moon 65125 Long COVID Severe at worst reddit.com Oct 2026

    After a third COVID infection they had significant shortness of breath, dizziness, exercise intolerance, tachycardia and hypertension, then became unable to walk and extremely sick for months after hiking and a COVID/flu vaccine. Six months of searching…

  • Bedbound with ME/CFS, now housebound and somewhat better with rest and low-dose naltrexone

    Somewhat better Maple 86872 ME/CFS Severe at worstIll 18 months before improving or writing reddit.com Oct 2026

    After about 1.5 years of ME/CFS with push–crash cycles, they became bedbound for two months in mid-2026, getting up only for the bathroom. They improved slowly with four months of rest, low-dose naltrexone, a beta-blocker, compression and salt/fluids. By…

  • Bedbound with ME/CFS for over a year, now partly better with pacing and LDN

    Somewhat better Prairie 49039 ME/CFS Very severe at worstIll 4.5 years before improving or writing reddit.com Oct 2026

    A Dutch long-hauler became ill with COVID in mid-2022 and was bedbound, in bed around the clock, for over a year. Rest and pacing, a 75% vegetable diet that fixed their gut, NAC for brain fog, LDN for PEM and ivabradine for POTS brought slow, partial gains.…

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