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ME/CFS Outcome unclearNeeds ongoing treatment

ME/CFS overdoing activity, pacing and stimulants help manage

Condition
ME/CFS
At worst
Mild (working or studying, with limits)
Ill for
Not stated
Last post
Aug 2026
In their words
  • Condition: ME/CFSSometimes I feel like I have a lot of spoona so I take up more activities and while doing them I feel good and right after ending it, I realized that I have overdone it In context ↗
  • At worst: MildSometimes I feel like I have a lot of spoona so I take up more activities and while doing them I feel good and right after ending it, I realized that I have overdone it In context ↗
Read from 4 of their posts and comments; links to the 3 this page draws on

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Summary

Badger 50118 struggles with overdoing activity, realising only afterwards that a task was too much. They pace by cooking seated, using an Easi-Grip knife and anti-slip mat, and suggest sitting or leaning against the counter for dishwashing. They set vibration alarms to check in with their body. They describe stimulants as helping a lot, quietening head noise and improving proprioception so pacing is a little easier to manage.

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What they tried

Also tried

stimulants· Helpedpacing· Helpedinteroception training· Helped
Their words about each treatment
  • stimulants · HelpedHonestly for me it helps a lot. Without my stimulants I have a lot more going on in my head and stressing out over a lot of things. My proprioception is a lot better with my meds than without it. In context ↗
  • pacing · HelpedGenerally what helps me most: Try to do everything seated or at least against something. I did not notice how much energy my body used just for standing up. In context ↗
  • interoception training · HelpedI am also training that. I am a lot better now with realizing that something is bad for me than before. I set little vibration alarms for checkins. In context ↗

Their path

They say too little about how ill they were at each step to draw it on the severity scale, so the steps are listed as they describe them. Dates are when they posted.

WhenWhat happenedWhere they wereAfter
—ME/CFS, seen by an ME specialistI relate to you so much as I struggle with the aame thing In context ↗Not stated
2026-08-27stimulants quieten head noise and improve proprioception, making pacing easierMy proprioception is a lot better with my meds than without it. So pacing is a little bit better to manage for myself than without it. In context ↗MildStimulants (unspecified)

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseSometimes I feel like I have a lot of spoona so I take up more activities and while doing them I feel good and right after ending it, I realized that I have overdone it. In context ↗
  • Anxiety & low moodWithout my stimulants I have a lot more going on in my head and stressing out over a lot of things. In context ↗

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