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ME/CFS Mild → no benefitIll for 4 yearsNeeds ongoing treatment

ME/CFS, rarely leaving home to socialise, caffeine brought no improvement

Condition
ME/CFS
At worst
Mild (working or studying, with limits)
Ill for
4 years
Last post
Jan 2024
In their words
  • Condition: ME/CFSI don’t have any negative effects from having coffee unlike a lot of people with cfs/me x In context ↗
  • At worst: MildI generally have 1 cup in the morning and if I’m leaving the house to socialise it usually involves coffee, but that is very rare. In context ↗
  • Now: No benefitYes caffeine keeps me human. I don’t drink it everyday but need it to get me through the week lol. In context ↗
Read from 2 of their posts and comments; links to the 2 this page draws on

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Summary

A person with ME/CFS said caffeine kept them human: about one cup in the morning, not every day, helped them get through the week with no negative effects, and leaving the house to socialise was very rare. A support group they attended about four years after onset was depressing; they preferred friends from a local ME/CFS Facebook group.

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What they tried

Also tried

Their words about each treatment
  • caffeine · HelpedI generally have 1 cup in the morning and if I’m leaving the house to socialise it usually involves coffee In context ↗

Their path

Very severeSevereModerateMildNear normalRecoveredonset12 mo2 y3 y4 y

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. Dates are when they posted. What the levels mean.

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WhenWhat happenedWhere they were
~2020ME/CFS onsetabout 4 years after onset In context ↗Mild
2024-01-14still ill; found a support group depressingI went to a support group at a similar time to you, about 4 years after onset In context ↗Mild

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