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ME/CFS Severe → somewhat better

Mostly bedridden with ME/CFS, now somewhat better with rest and screen settings

Condition
ME/CFS
At worst
Severe (mostly bedbound)
Ill before improving or writing
Not stated
Last post
Jul 2026
In their words
  • Condition: ME/CFSAs if GET didn’t get me here in the first place. In context ↗
  • At worst: SevereFirst time out of bed in a few weeks. The exertion made me throw up. ... I’m exhausted purely from toileting and drinking enough meal replacement shakes. In context ↗
  • Now: Somewhat betterMy capacity fluctuates hugely. ... Rest. Just a shite tonne of rest with as little stimulation as possible. It’s the only thing that reliably, gradually helps my baseline
Read from 6 of their posts and comments; links to the 5 this page draws on

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Summary

Beech 70088 has ME/CFS and in April 2026 was mostly bedridden, having been out of bed only once in a few weeks; that bath made them vomit and they blamed graded exercise for getting them there. In June they could look at a screen and post on Reddit again, and their capacity fluctuated hugely. By July they said phone and tablet settings made screens bearable, and that a huge amount of rest with as little stimulation as possible reliably helped their baseline.

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What they tried

What they credit

Also tried

coloured cellophane· No changeyawning to flush brain waste· WorseGET· Much worse
Their words about each treatment
  • GET · Much worseAs if GET didn’t get me here in the first place. In context ↗
  • rest · HelpedJust a shite tonne of rest with as little stimulation as possible. It’s the only thing that reliably, gradually helps my baseline In context ↗
  • yawning to flush brain waste · WorseOk so I tried this too and got acid reflux In context ↗
  • coloured cellophane · No changeI’ve tried coloured cellophane (LOL) and it doesn’t cut it In context ↗

Approaches: Radical rest

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 were
—ME/CFS onset, worsened by graded exerciseAs if GET didn’t get me here in the first place. In context ↗Not stated
2026-04-24in bed for weeks; a bath, first time out of bed in weeks, made them throw up; exhausted by toileting and shakesI had a bath a few days ago. First time out of bed in a few weeks. The exertion made me throw up. In context ↗Severe
2026-06-09able to look at a screen and post on Reddit againI’m flying high about being able to Reddit/look at a screen at the moment!! In context ↗Severe
2026-07-14capacity still fluctuates hugely; tablet settings make screens bearablethe settings on my phone/tablet make things bearable to look at In context ↗Severe

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseThe exertion made me throw up. In context ↗
  • Light & noise sensitivityI’ve tried coloured cellophane (LOL) and it doesn’t cut it In context ↗
  • Gut problemsOk so I tried this too and got acid reflux In context ↗

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