Miruvor
Sign up
ME/CFS Near normal

ME/CFS with neuropathy and fatigue, almost back to normal after learning to talk to body

Condition
ME/CFS
At worst
Not stated
Ill before improving or writing
Not stated
Last post
Jul 2024
In their words
  • Now: Near normalOnce i learnt to talk to my body all my symptoms have nearly gone. If i get a bit stressed they come back but way less. In context ↗
Read from 3 of their posts and comments; links to the 3 this page draws on

Request to remove this story

Summary

A person with gut dysbiosis described flaring neuropathy and fatigue around the time they stopped low-dose naltrexone, which they had used for over a year; they were unsure whether LDN caused the flare and planned to restart. By mid-2024 they reported that learning to talk to their body had nearly cleared their symptoms, which returned only mildly under stress.

Ask Miruvor AI

Asking aboutSandpiper 27165’s story

What they tried

Their words about each treatment
  • bacillus subtilis · No changeI have tried bacillus subtilis and it has still not gone away. In context ↗
  • LDN · No changeThe first time i took Ldn i had all these crazy symptoms and now i started it again and nothing. In context ↗
  • talking to my body · Helped a lotOnce i learnt to talk to my body all my symptoms have nearly gone. If i get a bit stressed they come back but way less. In context ↗

Approaches: Brain retraining

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
—illness onset, date not statedI have the same problem. In context ↗Not stated
2024-02-10neuropathy and fatigue flared up after switching LDN to night time and stopping itI actually still feel really bad so not sure it was the ldn so now im gonna start again and see if it the neuropathy and fatigue that's flared up goes down again. In context ↗Not stated
2024-07-31learnt to talk to their body; all symptoms nearly goneOnce i learnt to talk to my body all my symptoms have nearly gone. If i get a bit stressed they come back but way less. In context ↗Near normal

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Neuropathy & tinglingthe neuropathy and fatigue that's flared up In context ↗
  • Gut problemsI have dysbiosis and ldn In context ↗
  • Anxiety & low moodI found out I have a oversensitized nervous system probably caused by health anxiety. In context ↗

Ask Miruvor AI

Asking aboutSandpiper 27165’s story

Similar stories

  • Long COVID fatigue and tachycardia; kambo and ivermectin helped early, then relapse

    Relapsed Birch 29532 Long COVID Severe at worstIll 16 months before improving or writing reddit.com Oct 2026

    Birch 29532 caught COVID in early 2021 and developed long COVID with tachycardia; after a third infection during pregnancy she became debilitated by fatigue four months after her baby was born in January 2025. Mould avoidance and low-dose naltrexone didn't…

  • Long COVID too faint to walk or drive, now good most days at about 80-85%

    Much better Grove 43730 Long COVID Moderate at worstIll 6 months before improving or writing reddit.com Oct 2026

    A woman who fell ill with long COVID in August 2023 was too faint to walk around much or drive, with brain fog, breathlessness and anxiety. Quitting her job and resting six months, plus supplements, brought her to about 90% by mid-2024, but a January 2025…

  • Bedridden with ME/CFS at 5% capacity, now much better after nervous system rehab

    Much better Dune 25508 ME/CFS Very severe at worstIll 3 years before improving or writing reddit.com Oct 2026

    Fell ill in late 2023 at age 17 with severe insomnia and anxiety, then mononucleosis in April 2024 and a total collapse in September 2024 after social harassment and a breakup. Bedridden at about 5% capacity with brain fog, POTS, PEM and MCAS-like reactions,…

  • Bedbound most of the day with ME/CFS, now somewhat better after self-led trauma work

    Somewhat better Owl 71555 ME/CFS Severe at worst reddit.com Oct 2026

    Owl 71555 has had ME/CFS since childhood and was bedbound 80-90% of the day with constant severe brain fog before two years of self-led trauma work. That work improved gut function, cognition, muscle pain and migraines; they now spend about eight hours a day…

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