Miruvor
Sign up
ME/CFS Severe → no benefitIll for 14 months

Suspected ME/CFS with POTS, in bed 80-90% of time, revision surgery brought no improvement

Condition
ME/CFS
At worst
Severe (mostly bedbound)
Ill for
14 months
Last post
Feb 2026
In their words
  • Condition: ME/CFSNote I'm not diagnosed yet but like, I have confirmed POTS and everything else lines up to point to ME too. In context ↗
  • At worst: SevereCurrently mod-severe, in bed 80-90% of the time. In context ↗
  • Now: No benefitStarted mild in the aftermath of surgery and have only gotten worse in the last year In context ↗
  • Began after: COVIDI think getting COVID the month before was a much bigger factor, and surgery just compounded on top of it.
Read from 1 of their posts and comments; links to the one this page draws on

Request to remove this story

Summary

Beech 87707 became ill in late 2024 after sex reassignment surgery, with a COVID infection the month before. It started mild and worsened over the following year, partly through pushing themselves early on; by February 2026 they were in bed 80-90% of the time, with confirmed POTS and suspected ME/CFS. A revision surgery about 11 months later went smoothly with no baseline deterioration.

Ask Miruvor AI

Asking aboutBeech 87707’s story

What they tried

Their words about each treatment
  • pushing myself a lot early on · Worsehave only gotten worse in the last year, but a lot of that is because I pushed myself a lot early on In context ↗

Their path

Very severeSevereModerateMildNear normalRecoveredonset6 mo12 mo

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.

Show as a table
WhenWhat happenedWhere they were
late 2024fell ill after sex reassignment surgery, with COVID the month beforeStarted mild in the aftermath of surgery and have only gotten worse in the last year In context ↗Mild
2026-02-02worsened over the year, partly from pushing herself early on; in bed 80-90% of the timeCurrently mod-severe, in bed 80-90% of the time. In context ↗Severe

Symptoms mentioned

Their words about their symptoms
  • POTS & dysautonomiaI have confirmed POTS and everything else lines up to point to ME too In context ↗
  • Post-exertional malaisea lot of that is because I pushed myself a lot early on In context ↗

Ask Miruvor AI

Asking aboutBeech 87707’s story

A little hope, every Sunday

New recovery stories and data-driven research on ME/CFS and long COVID. Ideas worth considering, and the evidence behind them.

Free · Unsubscribe anytime