Miruvor
Sign up
Long COVID Moderate → much betterIll 6 months before improving or writing

Long COVID with constant facial nerve pain, now much better and able to exercise again

Condition
Long COVID
At worst
Moderate (mostly housebound)
Ill before improving or writing
6 months
Last post
Feb 2022
In their words
  • Condition: Long COVIDmy journey started in August 2021 with a mild infection In context ↗
  • At worst: ModerateI had to stop working after that because of constant pain and since then I'm worried of further crashes that's why I reduced my activities to a minimum In context ↗
  • Now: Much betterAll the other symptoms have vanished by now I even can exercise again but the nerve pain is still awful In context ↗
  • Began after: COVIDmy journey started in August 2021 with a mild infection In context ↗
Read from 5 of their posts and comments; links to the 5 this page draws on

Request to remove this story

Summary

A Reddit user fell ill in August 2021 after a mild infection with dizziness, a racing heart, fatigue and headaches. A crash while trying to return to normal life brought constant facial nerve pain and forced them to stop working and cut activity to a minimum. By February 2022 all symptoms except nerve pain in the face and right foot had gone and they could exercise again; amitriptyline and Lyrica had not helped.

Ask Miruvor AI

Asking aboutKite 23035’s story

What they tried

Their words about each treatment
  • being more active and doing sports · Much worseYes I definitely overdid it and I have since then this almost constant facial pain. Of course this happened after a doctor told me to be more active and to do sports... In context ↗
  • reducing activities to a minimum · HelpedI reduced my activities to a minimum and haven't crashed again In context ↗
  • amitryptiline · No changeSo far I've tried amitryptiline and lyrica but they both didn't help. In context ↗
  • lion's Mane · No changeI've tried lion's Mane but without any effect In context ↗
  • B complex · Not saidI'm taking a B complex already 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
August 2021fell ill after a mild infection with dizziness, racing heart, fatigue and headachemy journey started in August 2021 with a mild infection In context ↗
2021-11-09crashed after trying to get back to old life, developed constant facial nerve pain and stopped workingI had to stop working after that because of constant pain and since then I'm worried of further crashes that's why I reduced my activities to a minimum In context ↗
2022-02-19all symptoms except nerve pain gone; could exercise againAll the other symptoms have vanished by now I even can exercise again but the nerve pain is still awful In context ↗

Adverse events

  • Everyday exercise and activity“Yes I definitely overdid it and I have since then this almost constant facial pain. Of course this happened after a doctor told me to be more active and to do sports...” In context ↗ Made symptoms worse

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI did have one major crash when I was trying hard getting back to my old life and indeed felt fatigued the day after In context ↗
  • Headaches & migrainemy main symptoms for the first three months were dizziness, heart palpitations, fast heart beat, fatigue and headache In context ↗
  • Heart symptoms & palpitationsheart palpitations, fast heart beat In context ↗
  • Neuropathy & tinglingthe nerve pain is still awful In context ↗

Ask Miruvor AI

Asking aboutKite 23035’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