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ME/CFS Mild → no benefitIll for 3 years

Three years with ME/CFS, working full time on the razor's edge, no benefit from pills

Condition
ME/CFS
At worst
Mild (working or studying, with limits)
Ill for
3 years
Last post
Jan 2021
In their words
  • Condition: ME/CFSeven though I'm diagnosed me with ME, I still don't know what exactly I have In context ↗
  • At worst: MildRight now I'm on the razor's edge of being able to work a full-time job and that's mostly due to being able to work from home In context ↗
  • Now: No benefitIf anything I feel worse today than I did six months ago In context ↗
  • Began after: nothing they could nameIt's been 3 years since I first had symptoms of fatigue/brain fog/etc. 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 three years into ME/CFS, diagnosed at Stanford, spent six months on a daily cocktail of CoQ10, acetyl-L-carnitine, curcumin, naltrexone 50 mg and aripiprazole 0.75 mg. They felt worse than before starting it, unsure whether the pills, inactivity or the disease itself was to blame. They were still working full time from home, on the razor's edge of managing, and were ready to give up on the pills.

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What they tried

Their words about each treatment
  • CoQ10 · Not saida daily cocktail of CoQ10, Acetyl L-Carnitine, Curcumin, Naltrexone (50mg) and Aripiprazole (Ability) 0.75mg 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
2018first symptoms of fatigue and brain fogIt's been 3 years since I first had symptoms of fatigue/brain fog/etc. In context ↗Not stated
2021-01-22six months on a Stanford supplement and drug cocktail, feeling worse than before, still working full-time from homeIf anything I feel worse today than I did six months ago In context ↗Mild

Symptoms mentioned

Their words about their symptoms

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