Miruvor
Sign up
ME/CFS Somewhat betterIll 10 years before improving or writing

ME/CFS for ten years, somewhat better after diet changes

Condition
ME/CFS
At worst
Not stated
Ill before improving or writing
10 years
Last post
Sep 2024
In their words
  • Condition: ME/CFSI’ve had CFS for ten years now In context ↗
  • Now: Somewhat betterWhen I started feeling better, I tried to introduce everything back in over time. In context ↗
Read from 3 of their posts and comments; links to the 3 this page draws on

Request to remove this story

Summary

The user had had CFS for ten years by September 2024. Soon after diagnosis they changed their diet, trying paleo and cutting out dairy, gluten and other foods they did not tolerate; they said it really helped and later reintroduced foods as they felt better. They also mixed tea tree, rosemary and lavender oils into their shampoo and conditioner, which helped hair growth. They were still investigating possible narcolepsy.

Ask Miruvor AI

Asking aboutZephyr 40693’s story

What they tried

What they credit

Also tried

tea tree, rosemary and lavender essential oils· Helped
Their words about each treatment
  • paleo diet · HelpedI tried a paleo diet for a while; cut out dairy, gluten, and other foods that my body didn’t do well with and it really helped. In context ↗
  • tea tree, rosemary and lavender essential oils · HelpedI mixed them into my shampoo and conditioner each time i showered and it especially helped with hair growth In context ↗

Approaches: 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 happenedAfter
2014onset of CFSI’ve had CFS for ten years now In context ↗
when I was first diagnosedchanged diet and felt betterI tried a paleo diet for a while; cut out dairy, gluten, and other foods that my body didn’t do well with and it really helped. In context ↗Elimination diets (other)
2024-09-19still has CFS, investigating possible narcolepsyam now figuring out that i may also have narcolepsy In context ↗

Symptoms mentioned

Their words about their symptoms
  • Hair lossWhen this happened to me i started trying tea tree, rosemary and lavender essential oils. In context ↗

Ask Miruvor AI

Asking aboutZephyr 40693’s story

Similar stories

  • 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,…

  • Bedbound for months with ME/CFS, now much better after vein surgeries and physical therapy

    Much better Beacon 84978 ME/CFS Very severe at worstIll 3.5 years before improving or writing reddit.com Oct 2026

    A 29-year-old man's long COVID began in mid-2021 after his second Pfizer dose and worsened for three years; an early-2024 presumed reinfection left him 95% bedbound for months, and he has been unable to work for over three years. Vein surgeries, compression…

  • Long COVID with POTS and brain fog, improved then relapsed, now mostly housebound

    Relapsed Glade 14161 Long COVID Severe at worstIll 4 years before improving or writing reddit.com Oct 2026

    A teenager developed POTS, vertigo and brain fog after COVID in 2022, then had a near two-year remission. A reinfection in late 2024 left her disabled, and further infections plus a decline into ME-type crashes with light and sound sensitivity made her…

  • Bedbound at worst with ME/CFS after COVID, now somewhat better with pacing

    Somewhat better Vale 94777 ME/CFS Severe at worstIll 4 years before improving or writing reddit.com Oct 2026

    A person in New Zealand became ill with COVID around mid-2022. They worsened for 14 months to severe and bedbound, and are not working. Pacing, an electric wheelchair, mast-cell and arthritis drugs, and vitamin D later brought them to mild (moderate side of…

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