Miruvor
Sign up
ME/CFS Moderate → somewhat better

Moderate ME/CFS with buzzing nerves, somewhat better after low-dose naltrexone

Condition
ME/CFS
At worst
Moderate (mostly housebound)
Ill before improving or writing
Not stated
Last post
Jan 2024
In their words
  • At worst: ModerateCFS is still moderate, but that symptom itself faded In context ↗
  • Now: Somewhat betterit is nearly gone. Still have all other symptoms pretty bad In context ↗
  • Began after: nothing they could nameI don't know what triggered my CFS, possibly from my Hashimoto's (found that I had hashis while investigating my CFS symptoms). In context ↗
Read from 27 of their posts and comments; links to the 22 this page draws on

Request to remove this story

Summary

A Reddit user described moderate ME/CFS with Hashimoto's, a buzzing nerve sensation, muscle twitching, heat intolerance and constipation. Low-dose naltrexone, slowly raised to 5 mg, was followed by the buzzing largely fading, though they were unsure it was the cause. Oxaloacetate gave no benefit. Work was capped at 12 hours a week before symptoms flared.

Ask Miruvor AI

Asking aboutVale 70095’s story

What they tried

Their words about each treatment
  • meditation · No changeAfter trying everything (drugs, meditation, alcohol) to escape with nothing working In context ↗
  • alcohol · WorseI feel like trash immediately after one drink. Tried many times just to feel different as an escape In context ↗
  • dessicated thyroid · HelpedNow I'm on thyroid meds and my weight came back down to normal. In context ↗
  • electrolytes and minerals · Not saidMy electrolytes are great as I take lots of them and also do IV therapy In context ↗
  • Myers IV therapy · No changeI do 100ml Myers IV therapy (lots of B vitamins I think). Don't notice any major help In context ↗
  • glutathione push · No changeAlso get a glutathione push at the end which is supposed to help detox. But yeah, not life changing In context ↗
  • laxatives · No change3 weeks of laxatives for constipation that had no effect In context ↗
  • Citro-mag (high dose magnesium citrate) · HelpedCitro-mag (high dose magnesium citrate) over enema for sure, clears everything out In context ↗
  • plunges in the river · HelpedI've just started doing plunges in the river by my house (~0°C) and I love it. In context ↗
  • acupuncture · HelpedJust started doing acupuncture which is helping a little. In context ↗
  • high CBD weed · HelpedJust started to smoke high CBD weed which is actually helping, really sick at the moment though, so taking a break from that. In context ↗
  • LDN (low dose naltrexone) · HelpedAfter 4 months of gradually increasing LDN, (2 or so years after it all started) it is nearly gone. In context ↗
  • ice hats · HelpedIce hats have saved me In context ↗
  • light yoga · HelpedYeah light yoga. Sometimes it's pretty much impossible, but I try to do 15mins a day. Really helps with general mobility. In context ↗
  • voltaren · Not saidNow I just have tons of electrolytes ,use voltaren and tiger balm. In context ↗
  • muscle gun · Not saidI also have a muscle gun that I use lightly to loosen things up. In context ↗
  • Jameson probiotics (Costco) · HelpedI find that one of the cheapest ones works best for me (by far). In context ↗
  • steam room · HelpedI have heat intolerance as well but find the steam actually helps. In context ↗
  • super sleep tabs from Webber naturals · Not saidI also take super sleep tabs from Webber naturals, because I did find it harder to stay asleep. In context ↗
  • oxaloacetate (benaGene) · No changeEven oxaloacetate at 2000mg a day had no positive effect In context ↗

Their path

Very severeSevereModerateMildNear normalRecoveredonset12 mo2 y3 y4 y

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
onsetME/CFS began, cause unknown, alongside Hashimoto'sI don't know what triggered my CFS, possibly from my Hashimoto's (found that I had hashis while investigating my CFS symptoms). In context ↗Moderate
1.5 years inbuzzy nerve sensation largely fadedMine went away after 1.5 years. Only get little bits of it now. In context ↗Moderate
2023-10-17returned to work, capped at 12 hours a weekI just started returning to work though and noticed that it comes back a bit stronger the more I work. My body seems capped at working 12h a week In context ↗Moderate
2024-01-12still ill; naps bring on flu-like symptomsYeah, naps are a no go for me. Flu symptoms for a couple hours after In context ↗Moderate

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Neuropathy & tinglingI'd say my nerve issues. That buzzy feeling. I had that really bad before. In context ↗
  • Post-exertional malaisemy body proved me wrong and 12h/wk was the max I could do sustainably without getting sick every week In context ↗
  • Temperature regulationI have heat intolerance as well but find the steam actually helps. In context ↗
  • Flu-like symptomsYeah, naps are a no go for me. Flu symptoms for a couple hours after In context ↗
  • Gut problemsgave me relief after 3 weeks of laxatives for constipation that had no effect In context ↗
  • Sleep problemsI did find it harder to stay asleep In context ↗
  • Vision problemsYes. I used to get that a lot. In context ↗
  • Pain & fibromyalgiaI get that too. Tried everything you mentioned and none of that works. In context ↗

Ask Miruvor AI

Asking aboutVale 70095’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