Miruvor
Sign up
ME/CFS Much better

ME/CFS, now much better with functional medicine and diet change

Condition
ME/CFS
At worst
Not stated
Ill before improving or writing
Not stated
Last post
Apr 2021
In their words
  • Condition: ME/CFSI’ve been diagnosed for 1.5 years In context ↗
  • Now: Much betterI’ve improved so much through a variety of diet change, acupuncture and acceptance. In context ↗
Read from 2 of their posts and comments; links to the 2 this page draws on

Request to remove this story

Summary

Reddit user Eagle 29413 was diagnosed with ME/CFS about 1.5 years before their February 2020 post, when they said they had improved so much through a variety of diet change, acupuncture and acceptance. In April 2021 they wrote that functional medicine, which they note is considered alternative rather than mainstream, had really helped them.

Ask Miruvor AI

Asking aboutEagle 29413’s story

What they tried

Their words about each treatment
  • diet change · HelpedI’ve improved so much through a variety of diet change, acupuncture and acceptance In context ↗
  • functional medicine · HelpedFunctional medicine is considered ‘alternative’ and it’s really helped me. In context ↗

Approaches: CBT & mindset · Alternative therapies · Diet

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
2018diagnosed with ME/CFS (1.5 years before their February 2020 post)I’ve been diagnosed for 1.5 years In context ↗
2020-02-11improved so much with diet change, acupuncture and acceptanceI’ve improved so much through a variety of diet change, acupuncture and acceptance In context ↗
2021-04-05says functional medicine has really helped themFunctional medicine is considered ‘alternative’ and it’s really helped me. In context ↗

Ask Miruvor AI

Asking aboutEagle 29413’s story

Similar stories

  • Not enough detail to draw a path

    Long COVID with 15 daily symptoms, now somewhat better after gut protocol and diet

    Somewhat better Cardinal 18236 Long COVID Mild at worstIll 2 years before improving or writing reddit.com Mar 2026

    Cardinal 18236 has had long COVID since February 2024; at worst they had around 15 daily symptoms including insomnia, swallowing trouble, anxiety, brain fog and POTS. By around 10 months, a functional-medicine gut protocol, diet change, low-level daily…

  • Long COVID gut problems, few foods and unable to walk a block some days, now recovered

    Recovered Cedar 51238 Long COVID Moderate at worstIll 2 months before improving or writing reddit.com Feb 2025

    Cedar 51238 had gut problems for seven years before a Covid infection flared them badly; she could eat only a few plain foods such as chicken, sweet potatoes and zucchini, and some days could not walk a block. She credits an elimination diet, l-glutamine,…

  • Long COVID at worst unable to care for herself, now much better and working full time

    Much better Meadow 59098 Long COVID Severe at worstIll 10 months before improving or writing reddit.com Nov 2024

    A 36-year-old woman developed long COVID after a COVID infection in April 2023; at her worst she could not drive or care for herself and was off work for six months. Over the next year she used low-dose naltrexone, NAC, Botox, stellate ganglion blocks,…

  • Unable to walk around house with long COVID, much better after pacing and antihistamines

    Much better Falcon 84129 Long COVID Severe at worstIll 3 years before improving or writing reddit.com Oct 2026

    A Canadian man with long COVID for about three years was unable to walk around the house for the first two years, with constant migraines, brain fog and PEM. From year three, pacing, rest, stress reduction, H1/H2 antihistamines, hydroxyzine for sleep,…

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