Miruvor
Sign up
Long COVID Somewhat betterIll 18 months before improving or writing

Long COVID symptoms for over a year, somewhat better with a Mayo-guided approach

Condition
Long COVID
At worst
Not stated
Ill before improving or writing
18 months
Last post
Jun 2021
In their words
  • Condition: Long COVIDI have since experienced multiple and on-going 'long haul' symptoms In context ↗
  • Now: Somewhat betterI'm improved but still not back to normal. In context ↗
  • Began after: another virusI had a viral infection in Dec. 2019 before Covid was widespread and before testing was available. In context ↗
Read from 3 of their posts and comments; links to the 2 this page draws on

Request to remove this story

Summary

Fell ill after a viral infection in December 2019, never confirmed as Covid, with multiple ongoing long-haul symptoms for over a year. After many tests and specialist referrals, Mayo Clinic diagnosed post-viral syndrome by elimination. With guidance from Mayo, they were taking a multi-pronged approach including supplements, CBD, slow cardio increases, red light therapy, hyperbaric oxygen and NAD+ infusions; by June 2021 they had improved but were not back to normal.

Ask Miruvor AI

Asking aboutGull 29669’s story

What they tried

Also tried

Their words about each treatment
  • supplements · Helpeda multi-pronged approach including supplements, full-spectrum CBD In context ↗
  • full-spectrum CBD · Helpedfull-spectrum CBD In context ↗
  • cardio exercise · Helpedslow and steady increases in cardio exercise In context ↗
  • proper hydration · Helpedproper hydration In context ↗
  • PBM - photobiomodulation or red light therapy · HelpedI do feel that PBM - photobiomodulation or red light therapy -- has helped me with 2x per week sessions. In context ↗
  • HBOT · HelpedI've had 2 HBOT sessions so far. ... I believe HBOT does help but to what extent, I cannot say. In context ↗
  • NAD+ iv infusion treatments · Not saidjust started NAD+ iv infusion treatments In context ↗

Approaches: Hyperbaric & oxygen · POTS medication · Alternative therapies · Other drugs and medicines · Physiotherapy and rehab

Their path

Very severeSevereModerateMildNear normalRecoveredonset6 mo12 mo18 mo

How ill they were on the ME/CFS severity scale, estimated from what they describe at each point, with time counted from when the illness began. Hover or tap a point. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
Dec. 2019viral infection; ongoing long-haul symptoms beganI had a viral infection in Dec. 2019 before Covid was widespread and before testing was available. In context ↗Mild
2021-06-29partial recovery after Mayo guidance; still not back to normalI'm improved but still not back to normal. In context ↗MildRed and near-infrared light therapy

Ask Miruvor AI

Asking aboutGull 29669’s story

Similar stories

  • Unable to walk or work with ME/CFS, now recovered after brain retraining

    Recovered Sequoia 85591 ME/CFS Severe at worstIll 2 years before improving or writing reddit.com Apr 2024

    Claire, a 24-year-old in France, became ill within 48 hours of a single Pfizer dose in July 2021; she could not walk or work for three weeks and had brain fog, neuropathy, POTS, insomnia and pain. She improved slowly, felt about 90% better after a COVID…

  • Long COVID with PEM after overdoing it, much better after pacing and time

    Much better Glacier 45175 Long COVID Severe at worst reddit.com Oct 2026

    He was a fit gym-goer in London who never recovered from a fifth COVID infection in March 2024. After about 18 months he improved to about 80-90% by walking daily, cutting sugar and alcohol, and taking mirtazapine, electrolytes, CBD oil and using red light…

  • Mostly bedbound with ME/CFS, now can sometimes sit upright and watch half a TV episode

    Somewhat better Alder 37129 ME/CFS Very severe at worstIll 18 years before improving or writing reddit.com Aug 2026

    Fell ill with ME/CFS years ago and worsened over time; by 2021 they were mostly bedbound, in a dark room with earplugs, and crashing from mental or sensory exertion such as screens, reading or too much thinking. They suspect POTS and were waiting for a…

  • Not enough detail to draw a path

    Bedridden with long COVID and POTS in 2021, now much better after ivabradine

    Much better Fjord 24173 Long COVID Severe at worstIll 3 years before improving or writing reddit.com Feb 2024

    This Reddit user developed POTS, diagnosed in 2021, on top of fibromyalgia that began at 22. They were bedridden for all of June 2021, then improved on the beta blocker ivabradine. By early 2024 they rated themselves about 85% better but not back to their…

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