Miruvor
Sign up
ME/CFS Mild → somewhat better

ME/CFS meant giving up full-time work, somewhat better after slow strength training

Condition
ME/CFS
At worst
Mild (working or studying, with limits)
Ill before improving or writing
Not stated
Last post
Dec 2023
In their words
  • Condition: ME/CFSEveryone tells me people with ME/CFS shouldn't exercise but it's literally working for me. In context ↗
  • At worst: MildI had to give up work full time so I started my own business on my terms. In context ↗
  • Now: Somewhat betterIt's made such a difference to my physical health but also my mental health. In context ↗
Read from 1 of their posts and comments; links to the one this page draws on

Request to remove this story

Summary

Coast 10005 had to give up full-time work and started their own business on their own terms. After 18 months of slow strength training at a steady heart rate, done carefully, they reported no flares and better physical and mental health. They said they would be as tired and in pain whether active or lying down, accepted pacing as a permanent norm, and were unsure about full recovery.

Ask Miruvor AI

Asking aboutCoast 10005’s story

What they tried

Also tried

Their words about each treatment
  • Pacing · Not saidPacing is obviously going to be the norm and that's fine. In context ↗
  • Slow strength training · HelpedI do slow strength training maintaining a steady heart rate. I've been doing it for 18 months without a single flare In context ↗

Approaches: Exercise and activity

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
—had to give up full-time work because of the illnessI had to give up work full time so I started my own business on my terms. In context ↗Mild
2023-12-2518 months of slow strength training with no flares; still tired and in pain, running own businessI've been doing it for 18 months without a single flare because I do it carefully and consciously. In context ↗MildStrength training

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI've been doing it for 18 months without a single flare because I do it carefully and consciously. In context ↗
  • Pain & fibromyalgiaI'm going to be as tired and as in pain whether I'm up and doing with a positive mindset or lying down, doing nothing In context ↗

Ask Miruvor AI

Asking aboutCoast 10005’s story

Similar stories

  • Exhausted and lying in bed with ME/CFS; fatigue lifted, then relapsed

    Relapsed Horizon 99824 ME/CFS Mild at worstIll 5 years before improving or writing reddit.com Oct 2026

    They were exhausted through college and until the past year, sleeping 10–14 hours a day and lying in bed. Within the past year the fatigue lifted to roughly 87% of normal, though they credited no specific treatment; they mentioned strength training, diet and…

  • Bedridden with ME/CFS, now much better with aggressive rest and immune globulin

    Much better Stream 28708 ME/CFS Severe at worstIll 10 years before improving or writing reddit.com Oct 2026

    Developed ME/CFS at 13 after mononucleosis and became bedridden with months of rolling PEM, worsened by exercise addiction and a COVID vaccine. Aggressive rest plus subcutaneous immune globulin (20 g/week), testosterone, growth hormone and peptides took him…

  • Moderate ME/CFS and unable to work, now somewhat better; sleep improved with amitriptyline

    Somewhat better Crane 49554 ME/CFS Moderate at worstIll 16 years before improving or writing reddit.com Sep 2026

    A UK man who fell ill in his early 20s with mononucleosis stayed mild for years while pushing through gym training, then became moderate. Amitriptyline 20-30mg, magnesium, morning caffeine and a regular sleep routine greatly improved his sleep; a short…

  • Long COVID with body-wide pain, somewhat better with protein and B vitamins

    Somewhat better Birch 50654 Long COVID Moderate at worst reddit.com Aug 2026

    Posting on ME/CFS forums, they described pain in every part of their body and said they were slowly getting better. They credited 100-130 g of protein daily, B vitamins, CoQ10 200 mg each morning, creatine, light strength training and journaling. Acupuncture…

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