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ME/CFS No benefit

ME/CFS with brain fog and fatigue; treatment brought no overall benefit and worse fatigue

Condition
ME/CFS
At worst
Not stated
Ill for
Not stated
Last post
Dec 2022
In their words
  • Condition: ME/CFSlike the CFS or things it causes me to to react to In context ↗
  • Now: No benefitOne week for me and my energy is still much worse than before, plus I have regular chest pains. In context ↗
Read from 4 of their posts and comments; links to the 4 this page draws on

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Summary

A Reddit user with CFS who reported trying something for months: brain fog improved noticeably, but fatigue became far worse and daily headaches appeared, so they stopped. In 2021 they said a week later their energy was still much worse than before, with regular chest pains. They said most medication side effects hit them harder than other people and made their CFS worse, so they could never stay on any long term.

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What they tried

Their words about each treatment
  • Low Dose Naltrexone · WorseMy brain fog was WAY better on it ... However, it made my fatigue infinity worse, and I got other side effects such as daily headaches In context ↗
  • COVID vaccination as treatment · WorseOne week for me and my energy is still much worse than before 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 happenedAfter
—Living with CFS; onset not datedlike the CFS or things it causes me to to react to In context ↗
2018-12-28Took low-dose naltrexone for months: brain fog much better but fatigue far worse and daily headaches, so stoppedMy brain fog was WAY better on it ... it made my fatigue infinity worse In context ↗Low-dose naltrexone
2021-08-11Coronavirus vaccine: a week later energy still much worse than before, plus regular chest painsOne week for me and my energy is still much worse than before, plus I have regular chest pains In context ↗
2022-12-28Still ill; cannot stay on medicines long term because their side effects worsen the CFSI've never been able to stay on any long term because ultimately they made my CFS worse In context ↗

Adverse events

Symptoms mentioned

Their words about their symptoms

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