Miruvor
Sign up
ME/CFS Mild → somewhat better

Brain fog, sleepiness and muscle soreness with ME/CFS, somewhat better with gabapentin

Condition
ME/CFS
At worst
Mild (working or studying, with limits)
Ill before improving or writing
Not stated
Last post
May 2017
In their words
  • Condition: ME/CFSAny tips on clearing brain fog? In context ↗
  • At worst: MildI'm taking community college courses while working 20 hrs a week (because I'm poor), so efficiency is key here. In context ↗
  • Now: Somewhat bettergabapentin (the less-potent predecessor to Lyrica) has greatly reduced my fatigue and morning stiffness, as well as some of my other, less frequent muscle pain In context ↗
Read from 2 of their posts and comments; links to the 2 this page draws on

Request to remove this story

Summary

A college student on medical leave described brain fog, sleepiness and muscle soreness in 2015, while working 20 hours a week and taking community college courses. Fibromyalgia was the closest label for their illness, and they said gabapentin greatly reduced their fatigue, morning stiffness and less frequent muscle pain.

Ask Miruvor AI

Asking aboutBramble 86717’s story

What they tried

Their words about each treatment
  • Ibuprofen · No changeIbuprofen and aspirin don't always help In context ↗
  • gabapentin · Helped a lotgabapentin (the less-potent predecessor to Lyrica) has greatly reduced my fatigue and morning stiffness, as well as some of my other, less frequent muscle pain In context ↗

Approaches: Other drugs and medicines

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
2015-08-14on medical leave from college, working 20 hrs a week and taking courses, brain fog and sleepinessI'm on "voluntary" medical leave from college ... taking community college courses while working 20 hrs a week In context ↗Mild
2017-05-11gabapentin reduced fatigue, morning stiffness and muscle pain; fibromyalgia the closest labelIt was the best approximation for me, and gabapentin ... has greatly reduced my fatigue and morning stiffness, as well as some of my other, less frequent muscle pain In context ↗Not stated

Symptoms mentioned

Their words about their symptoms
  • Brain fogMy main issue is getting work done w/o being too sleepy or foggy In context ↗
  • Sleep problemsbeing too sleepy or foggy In context ↗
  • Pain & fibromyalgiaIt was the best approximation for me ... has greatly reduced my fatigue and morning stiffness, as well as some of my other, less frequent muscle pain In context ↗

Ask Miruvor AI

Asking aboutBramble 86717’s story

Similar stories

  • Almost bedridden with ME/CFS, now much better after a specialist regimen and pacing

    Much better Fox 20038 ME/CFS Severe at worstIll 6.5 years before improving or writing reddit.com Oct 2026

    A California woman infected with COVID in March 2020 was sick six months, partly recovered, then relapsed and was almost bedridden by early 2023, unable to drive and sensitive to light and noise. An out-of-pocket ME/CFS specialist regimen of LDN, Abilify,…

  • Bedridden with long COVID for three years, now nearly back to normal with time and pacing

    Near normal Kite 59994 Long COVID Severe at worstIll 3 years before improving or writing reddit.com Oct 2026

    Caught COVID in December 2019, before lockdown, and was mostly bedridden for three years as symptoms worsened. From year three she improved slowly, crediting time, rest, pacing, a gradual walking programme, daily antihistamines and gabapentin. A 2023…

  • Fatigue and brain fog with ME/CFS, somewhat better with low-dose naltrexone and pacing

    Somewhat better Harbor 73697 ME/CFS Moderate at worstIll 2 years before improving or writing reddit.com Oct 2026

    Harbor 73697 fell ill in January 2023 with fatigue, brain fog and insomnia after an EBV infection at college, dropping out by April; POTS was diagnosed that summer. A COVID-like illness in late 2023 left her worse. Low-dose naltrexone and pacing were the…

  • Severe ME/CFS, unable to walk dog most days, much better on low-dose naltrexone

    Much better Ridge 96584 ME/CFS Severe at worst reddit.com Oct 2026

    Former competitive cheerleader with ME/CFS, fibromyalgia and POTS who said they were severe without medication, unable to walk their dog 400 m most days and crashed for days after 10 minutes of exercise. Low-dose naltrexone at 6 mg brought them to mild,…

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