Miruvor
Sign up
Long COVID Moderate → somewhat betterIll 2 years before improving or writing

Long COVID with vertigo, exhaustion and brain fog, somewhat better with diet and rest

Condition
Long COVID
At worst
Moderate (mostly housebound)
Ill before improving or writing
2 years
Last post
Dec 2022
In their words
  • Condition: Long COVIDI've had long covid since Jan 2021 In context ↗
  • At worst: Moderateit did make my long-covid infinitely worse. haven't been able to do much of anything since ... I've had to drastically reduce my work hours cuz my body just cannot handle much right now
  • Now: Somewhat betterWith proper diet, rest, vitamins etc, I'm doing much better. I do still get flare-ups and eventually I'll be on meds the rest of my life cause of it In context ↗
  • Began after: COVIDGot my first Covid infection Jan 3rd of 2021
Read from 9 of their posts and comments; links to the 5 this page draws on

Request to remove this story

Summary

Crocus 98294 developed long COVID after a COVID infection in January 2021, with vertigo, exhaustion, headaches, body aches, brain fog and insomnia. They improved by November 2021, but a second infection in January 2022 made their long COVID much worse and they cut their work hours. After a Hashimoto's diagnosis, they reported doing much better with diet, rest and vitamins by December 2022, though flare-ups continued.

Ask Miruvor AI

Asking aboutCrocus 98294’s story

What they tried

What they credit

Also tried

weed· Helped a lotproper diet· Helpedvitamins· Helpedlow-dose aspirin· No change
Their words about each treatment
  • weed · Helped a lotif I smoke a good sativa I can get stuff done I don't have the energy for In context ↗
  • low-dose aspirin · No changeI've been taking it as well since getting covid but unfortunately have not found the same relief In context ↗
  • proper diet · HelpedWith proper diet, rest, vitamins etc, I'm doing much better. In context ↗

Approaches: Pacing

Their path

What they say at each step doesn’t fit the worst point or outcome above on the severity scale, so the steps are listed as they describe them. Dates are when they posted.

WhenWhat happened
January 3, 2021first COVID infection, very ill for six weeksGot my first Covid infection Jan 3rd of 2021, was sick as a dog for 6 weeks. In context ↗
early 2021long COVID symptoms after the acute infectionAfter I "recovered" I had all the usual LH symptoms: vertigo, exhaustion, body aches, headaches, brain fog, the whole lot. In context ↗
November 2021getting back to normal, graduated barber school and got a new jobI felt like by November I was FINALLY getting back to normal. Just graduated Barber school, got a new job, things were good. In context ↗
January 2022second COVID infection made long COVID much worseit did make my long-covid infinitely worse. haven't been able to do much of anything since. In context ↗
December 2022doing much better with diet, rest and vitamins, still gets flare-upsWith proper diet, rest, vitamins etc, I'm doing much better. In context ↗

Symptoms mentioned

Their words about their symptoms
  • Headaches & migraineIt dulls the constant headaches In context ↗
  • Sleep problemsgood for combating this awful insomnia I've been plagued with In context ↗

Ask Miruvor AI

Asking aboutCrocus 98294’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,…

  • Mostly bedbound and housebound with ME/CFS, pacing and rest helped before a relapse

    Relapsed Valley 16092 ME/CFS Moderate at worstIll 25 years before improving or writing reddit.com Oct 2026

    Valley 16092 has had ME/CFS and fibromyalgia for about 25 years; stress and lifelong health problems led to a crash from 60-hour workweeks. They never became severe but have been mostly bedbound and housebound, and pacing, rest and comorbidity medication…

  • Mostly housebound with ME/CFS, now a little better on Klonopin and low-dose naltrexone

    Somewhat better Valley 89571 ME/CFS Moderate at worstIll 3 years before improving or writing reddit.com Oct 2026

    Joseph, 47, in Los Angeles, developed ME/CFS in January 2024, about 18 days after a second COVID infection. He declined from mild to the bad end of moderate over six months, becoming mostly housebound. Klonopin, low-dose naltrexone, midodrine and propranolol…

  • Long COVID brain fog, somewhat better with nicotine patch and naltrexone

    Somewhat better Pebble 25278 Long COVID Mild at worst reddit.com Oct 2026

    Pebble 25278 developed long COVID with brain fog, distorted smell, headaches, nerve pain and trouble sleeping. A quarter of a 10 mg nicotine patch restored much of their speech and thinking, and low-dose naltrexone further raised their cognitive and physical…

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