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ME/CFS Severe → somewhat betterNeeds ongoing treatment

Bedbound with ME/CFS, now somewhat better after travelling for help

Condition
ME/CFS
At worst
Severe (mostly bedbound)
Ill before improving or writing
Not stated
Last post
Oct 2026
In their words
  • Condition: ME/CFSI’d still be completely bed bound of if I didn’t keep looking for help. In context ↗
  • At worst: SevereI’d still be completely bed bound of if I didn’t keep looking for help. In context ↗
  • Now: Somewhat betterI’m one who has traveled for help and would continue to do so. I’d still be completely bed bound of if I didn’t keep looking for help. 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 ME/CFS said they would still be completely bed bound had they not kept travelling to look for help. A Lyme disease diagnosis was treated and cleared, but antibiotics left permanent side effects and they chose the herbal route. A visit a few years earlier was, they said, a waste of time and money that offered only pacing and counselling.

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What they tried

Also tried

Their words about each treatment
  • antibiotics · WorseI had this, eventually led to a Lyme disease dx. Treated and it went away. In context ↗
  • herbal route · Not saidI have permanent side effects from antibiotics so chose the herbal route. In context ↗
  • Mayo Clinic · No changeAlso went a few years ago and what a waste of time and money. 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
—completely bed bound before seeking helpI’d still be completely bed bound of if I didn’t keep looking for help. In context ↗Severe
2026-01-26travelling for medical help; no longer completely bed boundI’m one who has traveled for help and would continue to do so. In context ↗Not stated

Adverse events

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