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ME/CFS Moderate → no benefitIll for 10 years

Over 10 years with ME/CFS, too exhausted to get up; sleeping pills no help

Condition
ME/CFS
At worst
Moderate (mostly housebound)
Ill for
10 years
Last post
Feb 2022
In their words
  • Condition: ME/CFSI’ve been suffering with CFS for over 10 years now. In context ↗
  • At worst: ModerateI don’t wake up until the afternoon and I often don’t even go downstairs to get food and greet my family until 3-4pm In context ↗
  • Now: No benefitI’ve been suffering with CFS for over 10 years now. In context ↗
Read from 1 of their posts and comments; links to the one this page draws on

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Summary

A Reddit user who had had CFS for over 10 years described being too exhausted to get up while their brain was in overdrive 24/7. They could not work or enter education and often did not go downstairs until 3–4pm because they were too tired or lacked motivation. Sleeping pills made them more tired without helping them sleep.

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What they tried

Also tried

sleeping pills· Worse
Their words about each treatment
  • sleeping pills · WorseI’ve tried sleeping pills, but they don’t work. They just make me even more tired, yet still unable to sleep. 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 were
over 10 years before 2022CFS beganI’ve been suffering with CFS for over 10 years now. In context ↗Not stated
2022-02-16still unable to work or study; sleeps until afternoonI’m currently unable to work or enter education ... I don’t wake up until the afternoon In context ↗Moderate

Adverse events

  • “I’ve tried sleeping pills, but they don’t work. They just make me even more tired, yet still unable to sleep.” In context ↗ Side effects

Symptoms mentioned

Their words about their symptoms

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