Miruvor
Sign up
ME/CFS Moderate → no benefitIll for 1 yearNeeds ongoing treatment

Mild-to-moderate ME/CFS, mostly housebound, ivabradine gave no improvement

Condition
ME/CFS
At worst
Moderate (mostly housebound)
Ill for
1 year
Last post
Oct 2026
In their words
  • At worst: ModerateI’ve had pretty moderate/mild ME for about a year now and it progressed over that year. In context ↗
  • Now: No benefitwhen I’m off the vyvanse i can’t sleep at night, along with my chronic fatigue becoming utterly debilitating. In context ↗
Read from 5 of their posts and comments; links to the 4 this page draws on

Request to remove this story

Summary

Owl 43209 had had mild-to-moderate ME for about a year when diagnosed in September 2026, used a cane when leaving the apartment, felt more functional when mostly housebound, and also had fibromyalgia and IST. Slowing down and pacing gave more energy for chores, hygiene and online classes, and Vyvanse helped chronic fatigue, though they noticed low-grade fevers of unclear cause. Ivabradine did not work and metoprolol was not an option because it interacts with their antidepressants.

Ask Miruvor AI

Asking aboutOwl 43209’s story

What they tried

Their words about each treatment
  • pacing · HelpedI’ve noticed that this has helped me have energy to do household chores like dishes and cleaning In context ↗
  • vyvanse · HelpedAnd it does truly help me with my chronic fatigue, otherwise I’d be asleep all day haha In context ↗
  • ivabridine · No changeMy body did not respond to ivabridine In context ↗
  • antidepressants · Not saidmetoprolol interacts with my antidepressants In context ↗

Their path

Very severeSevereModerateMildNear normalRecovered12 mo13 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. The chart starts 12 months after onset: the story doesn’t say how ill they were before that. 1 step says too little to place on the scale and is only in the table. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
2025ME began and progressed over the yearI’ve had pretty moderate/mild ME for about a year now and it progressed over that year. In context ↗Not stated
September 2026mostly housebound, stopped working, needed a caneI stopped working to make time for my school which I had switched into online classes. ... I use a cane to get around *if* I leave my apartmentModerate
2026-10-01slowed down and paced, more energy for chores and classesthis has helped me have energy to do household chores like dishes and cleaning ... I’ve been able to keep up with my classwork In context ↗MildPacing and the energy envelope
2026-10-25Vyvanse keeping chronic fatigue manageable, but low-grade feversit does truly help me with my chronic fatigue, otherwise I’d be asleep all day haha In context ↗MildLisdexamfetamine (Vyvanse, Elvanse)

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseBut I also know I’d regret it if I crashed and got worse. In context ↗
  • Temperature regulationi feel really feverish and warm on and off In context ↗
  • Sleep problemswhen I’m off the vyvanse i can’t sleep at night In context ↗
  • Pain & fibromyalgiahaving been diagnosed with fibromyalgia for the past 7 ish years In context ↗

Ask Miruvor AI

Asking aboutOwl 43209’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