Miruvor
Sign up
ME/CFS Moderate → somewhat better

ME/CFS with memory problems and crashes, somewhat better with Wellbutrin

Condition
ME/CFS
At worst
Moderate (mostly housebound)
Ill before improving or writing
Not stated
Last post
Sep 2026
In their words
  • Condition: ME/CFSI hope you can find something that will help you, MECFS is so hard already!!!! In context ↗
  • At worst: ModerateI still need to be on total rest ... it's really helpful for me and my carers
  • Now: Somewhat betterMy room has also transformed over time to better support my needs since getting sick and it actually makes me really happy to feel like I can function better. In context ↗
Read from 6 of their posts and comments; links to the 5 this page draws on

Request to remove this story

Summary

An ME/CFS patient who has carers and uses a whiteboard for an out-of-sight, out-of-mind memory problem. Her heart rate stays elevated during crashes, which she uses to judge whether she can return to normal activity or needs total rest. She takes Saccharomyces boulardii with antibiotics to prevent yeast overgrowth. Wellbutrin helped her feel more like herself and would be the last prescription she would drop.

Ask Miruvor AI

Asking aboutMesa 90371’s story

What they tried

What they credit

Also tried

Their words about each treatment
  • Saccharomyces Boulardii · HelpedI always take it when I take antibiotics and I believe it prevented yeast overgrowth In context ↗
  • antibiotics · Not saidI always take it when I take antibiotics In context ↗
  • total rest · Not saidI use it as an indicator of whether I'm ok to go back to "normal" activity or if I still need to be on total rest. In context ↗
  • Timothy and the Bateman Horne support group · HelpedSeconding Timothy and the Bateman Horne support group, they have helped me so much. In context ↗
  • Wellbutrin · HelpedWellbutrin has helped me a lot, it made me feel a bit more like 'myself'. In context ↗
  • Lexapro · Not saidI'm also taking Lexapro (was already on Lexapro before getting sick for perimenopausal rage). In context ↗

Approaches: Other antidepressants

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 happened
—onset of ME/CFS, date not givenI'm also taking Lexapro (was already on Lexapro before getting sick for perimenopausal rage). In context ↗
2026-07-27adapted her room to support her needs and felt she could function betterMy room has also transformed over time to better support my needs since getting sick and it actually makes me really happy to feel like I can function better. In context ↗
2026-09-19Wellbutrin made her feel a bit more like herselfWellbutrin has helped me a lot, it made me feel a bit more like 'myself'. In context ↗

Symptoms mentioned

Their words about their symptoms
  • Heart symptoms & palpitationsMy heart rate stays elevated during a crash In context ↗
  • Brain fogotherwise I have a real 'out of sight/out of mind' problem In context ↗
  • Gut problemshaving had a past history of it In context ↗

Ask Miruvor AI

Asking aboutMesa 90371’s story

Similar stories

  • Long COVID crashes and wrecked gut, now near normal on antihistamines and diet

    Near normal Badger 97535 Long COVID Mild at worstIll 5.5 years before improving or writing reddit.com Oct 2026

    Badger 97535 developed long COVID after a covid infection in early 2021. He worked through months of 2-4 hours' sleep early on, a wrecked gut, mast cell reactions and flu-like crashes after exercise. Antihistamines, keto and very-low-calorie diets, PEA,…

  • Long COVID brain fog, fatigue and POTS, now much better with pacing and compression

    Much better Vale 64877 Long COVID Moderate at worstIll 17 months before improving or writing reddit.com Oct 2026

    A retired Northern California woman got long COVID in Italy in October 2024, with brain fog, fatigue, tinnitus and gut trouble; POTS was diagnosed later. Low-dose naltrexone, bupropion, acupuncture, osteopathy, pacing, salt and compression brought slow…

  • Mild ME/CFS while working, pain and brain fog somewhat better on low-dose naltrexone

    Somewhat better Harbor 37871 ME/CFS Mild at worst reddit.com Oct 2026

    Harbor 37871 describes themselves as a mild ME/CFS case who still works, pacing and resting to stay within their energy envelope. They take trazodone, sertraline plus bupropion, and low-dose naltrexone, which they say cut their pain and brain fog by 60-70%…

  • Bedbound for months with ME/CFS and POTS-like symptoms, now mostly normal on Strattera

    Near normal Starling 14544 ME/CFS Severe at worstIll 8 years before improving or writing reddit.com Oct 2026

    Starling 14544 became ill in the late 2010s in high school, declining until they left school in 2019 and were bedbound for months with POTS-like symptoms. Diagnosed with CFS at the Mayo Clinic in 2020, they found graded exercise, stretching and pacing made…

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