Miruvor
Sign up
Condition not stated Severe → much betterNeeds ongoing treatment

Brain fog and joint pain at 5-20% function, now much better on methylene blue

Condition
Condition not stated
At worst
Severe (mostly bedbound)
Ill before improving or writing
most of life
Last post
Jan 2026
In their words
  • Condition: Condition not statedI'm unsure if I have CFS but you be the judge In context ↗
  • At worst: Severefeeling like 5-20% daily to 60-90% daily In context ↗
  • Now: Much betterthe difference between feeling like 5-20% daily to 60-90% daily is a MASSIVE improvement In context ↗
  • Began after: nothing they could nameI've had brain fog the majority of my life too. In context ↗
Read from 1 of their posts and comments; links to the one this page draws on

Request to remove this story

Summary

Dove 78010, 33 and unsure about CFS, reported brain fog for most of their life, unrefreshing sleep, joint pain and function around 5-20%. Magnesium citrate 250 mg cut joint pain by about 80% and vitamin D3 2000 IU improved mood, but brain fog persisted. Methylene blue drops, started in early November, first caused odd vision and light-headedness; after a couple of weeks brain fog cleared and function rose to 60-90%, though ADHD remained.

Ask Miruvor AI

Asking aboutDove 78010’s story

What they tried

Their words about each treatment
  • workouts · Not saidI've tried everything stress free, workouts, medication In context ↗
  • trazodone · No changetrazodone (because I couldn't sleep). I wouldn't feel reset at all even when taking that. In context ↗
  • Sertraline · Not saidSertraline for depression to possibly help with sleep and depression. In context ↗
  • Magnesium Citrate · HelpedMagnesium Citrate 250Mg (Got rid of about 80% of my pain) In context ↗
  • Vitamin D3 · HelpedI was able to improve my mood by taking Vitamin D3 2000IU daily In context ↗
  • Methylene Blue · Helped a lotI've been on it since early Nov and it has been WORKING. ... My brain fog is gone, I can think and focus better. In context ↗
  • weed, CBD · Not saidSleep medication, prescriptions, weed, CBD, workouts, etc. In context ↗

Approaches: Other drugs and medicines

Their path

Very severeSevereModerateMildNear normalRecovered

How ill they were on the ME/CFS severity scale, estimated from what they describe at each point, in the order they describe; they don’t give enough times to place each step. Hover or tap a point. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
majority of my lifeLifelong brain fog, unrefreshing sleep and joint painI've had brain fog the majority of my life too. In context ↗Moderate
before early NovemberDaily function felt like 5-20% before methylene bluethe difference between feeling like 5-20% daily to 60-90% daily In context ↗Severe
after a couple of weeksAfter initial odd vision and light-headedness, brain fog cleared and function rose to 60-90%After those weeks everything became normal or what feels like normal. In context ↗MildMethylene blue
2026-01-19Still on methylene blue; brain fog gone, function 60-90%, ADHD remainsMy brain fog is gone, I can think and focus better. In context ↗MildMethylene blue

Adverse events

  • Methylene blue“The first couple of weeks it feels odd. For me it felt like it enhanced my vision and it kinda felt like sensory overload visually. It made me a bit light headed” In context ↗ Side effects

Symptoms mentioned

Their words about their symptoms

Ask Miruvor AI

Asking aboutDove 78010’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,…

  • Not enough detail to draw a path

    Long COVID with ME/CFS-like symptoms; some drugs helped, then it got worse again

    Relapsed Beacon 26144 Long COVID Ill 2 years before improving or writing reddit.com Oct 2026

    The person developed ME/CFS-like symptoms in 2024, with no stated trigger, and was still ill about two years later. They credit benzodiazepines, dextroamphetamine/Vyvanse, methylene blue, testosterone and cistanche with relief, and said some drugs made them…

  • Bedridden with ME/CFS, now much better after jaw infection treatment and iron infusion

    Much better Stone 43357 ME/CFS Severe at worstIll 10 years before improving or writing reddit.com Oct 2026

    Stone 43357 traced a decade of ME/CFS to a covid-like flu and was bedridden for days at a time for a couple of years. A dentist found a jawbone infection; treating the infection and an iron infusion brought most symptoms into remission. Creatine, a…

  • Bedbound with ME/CFS for three years, now much better with methylene blue

    Much better Hill 46448 ME/CFS Severe at worst reddit.com Oct 2026

    Undiagnosed mild ME/CFS for years, Hill 46448 became severe after a concussion and a crash that left her bedbound about three years, needing a power wheelchair and diapers. She credits compounded methylene blue most, alongside POTS drugs, LDN, NAD-ketamine…

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