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ME/CFS Severe → much betterIll 5 months before improving or writing

Couchbound with ME/CFS, now much better after a self-taught hormesis routine

Condition
ME/CFS
At worst
Severe (mostly bedbound)
Ill before improving or writing
5 months
Last post
Oct 2026
In their words
  • Condition: ME/CFSsince I got CFS (mar 2025) In context ↗
  • At worst: SevereI went from couchbound, severe headaches, muscle twitching, orthostatic intolerance, adrenaline spikes, sleeping maybe 12 hrs average and napping daily In context ↗
  • Now: Much betterI def still have cfs but it’s much better ... especially as someone who's mostly recovered too
  • Began after: stress or burnoutI cold turkeyed my medication (not intelligent) with absolutely brutal withdrawals and then got a cold during this along with college stress which finally sent me over the edge.
Read from 8 of their posts and comments; links to the 4 this page draws on

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Summary

Got CFS in March 2025, aged 21, after college stress, a cold and quitting an antidepressant; he was couchbound with headaches, orthostatic intolerance and brain fog. He credits a self-taught hormesis routine — nudging slightly above baseline then pulling back — for slow gains after a couple of months, later adding compression garments, salt, water, propranolol and LDN for sleep. By late 2026 he was mostly recovered but still had CFS.

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What they tried

Their words about each treatment
  • antidepressant · Not saidi was on an antidepressant which was hyper stimulating but for years I refused to get off it In context ↗
  • hormesis / nervous system stimulus reduction technique · Helped a loti started to notice that this technique did work after a couple months, literally everything made sense and progressed to a tee In context ↗
  • orthostatic compression garments · Not saidorthostatic compression garments In context ↗
  • High salt and water intake · Not saidHigh salt and water intake for orthostatic compression In context ↗
  • propranolol · Not saidpropranolol (as needed) In context ↗
  • audio neurofeedback · HelpedYou can even close your eyes while doing it, makes me feel more grounded and less anxious In context ↗
  • LDN · HelpedI’ve had success w LDN so far for my sleep!! In context ↗

Approaches: Brain retraining

Their path

Very severeSevereModerateMildNear normalRecovered17 mo19 mo

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. The first step with a time is 17 months after onset: the story doesn’t say how ill they were before that. The dashed part: the story doesn’t say when. 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 were
March 2025Got CFS after school stress, a cold and antidepressant withdrawalsince I got CFS (mar 2025) In context ↗Not stated
2025Couchbound with severe headaches, orthostatic intolerance, brain fog, napping dailyI went from couchbound, severe headaches, muscle twitching, orthostatic intolerance In context ↗Severe
Aug 2026Sleeping normal hours, socialising about an hour a day, limited part-time work and online classeswork a part time job (albeit very very limited hours), and I’m able to do my online classes at school In context ↗Mild
Oct 2026Says he is mostly recoveredespecially as someone who's mostly recovered too In context ↗Mild

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI stopped stressing about PEM or when I knew it was going to happen In context ↗
  • Brain fogbrain fog, impending doom feeling, forgetting words mid sentence In context ↗
  • Headaches & migrainesevere headaches In context ↗
  • POTS & dysautonomiaorthostatic intolerance In context ↗
  • Sleep problemssleeping maybe 12 hrs average and napping daily In context ↗
  • Anxiety & low moodimpending doom feeling In context ↗

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