Miruvor
Sign up
Long COVID Somewhat better

Long COVID with fatigue and heart-rate episodes, some improvement after vancomycin

Condition
Long COVID
At worst
Not stated
Ill before improving or writing
Not stated
Last post
Jan 2024
In their words
  • Condition: Long COVIDMy doctor and I thought maybe I had long covid as I kept getting episodes of really high resting heart rate as well as a bunch of other random symptoms. In context ↗
  • Now: Somewhat betterSince being on the antibiotics for c diff (vancomycin) I have felt so much! Better than I’ve felt in months if not years. In context ↗
  • Began after: COVIDMy doctor and I thought maybe I had long covid as I kept getting episodes of really high resting heart rate
Read from 3 of their posts and comments; links to the 3 this page draws on

Request to remove this story

Summary

They had episodes of very high resting heart rate with weakness, intense fatigue, chills and sweats, on top of nearly constant fatigue, and suspected long COVID. An ER visit found high white cells and low potassium, and a later test found a C. difficile infection. Vancomycin left them much better than in months or years, with no further heart-rate episodes except one day during a brief c diff recurrence, which was treated again.

Ask Miruvor AI

Asking aboutCrocus 40763’s story

What they tried

Their words about each treatment
  • physio · HelpedI did physio for it and it eventually calmed down. In context ↗
  • supplements · Not saidI take a lot of supplements for other reasons so perhaps some of those helped too. In context ↗
  • NAC · HelpedI love NAC. It’s probably the supplement I’ve taken the longest and most consistently. In context ↗
  • electrolytes by IV · Not saidGave me a bunch of electrolytes by IV In context ↗
  • antibiotics for c diff (vancomycin) · Helped a lotSince being on the antibiotics for c diff (vancomycin) I have felt so much! Better than I’ve felt in months if not years. In context ↗

Approaches: Antibiotics

Their path

Very severeSevereModerateMildNear normalRecovered

How ill they were on the ME/CFS severity scale, estimated from what they describe at each point, in the order they describe; they don’t give enough times to place each step. Hover or tap a point. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
—long-COVID-like illness with constant fatigue and episodes of very high resting heart rateI kept getting episodes of really high resting heart rate as well as a bunch of other random symptoms In context ↗Moderate
—worst heart-rate episode; went to ERMy last episode with high heart rate was really bad and I actually thought I may be having a heart attack In context ↗Severe
2024-01felt much better after vancomycin for c diff; brief c diff recurrence one day, treated againSince being on the antibiotics for c diff (vancomycin) I have felt so much! Better than I’ve felt in months if not years In context ↗MildVancomycin

Symptoms mentioned

Their words about their symptoms
  • Heart symptoms & palpitationsepisodes of really high resting heart rate In context ↗
  • Pain & fibromyalgiaI had some weird jaw and neck stuff this summer as well. I did physio for it and it eventually calmed down. In context ↗
  • Gut problemsI actually had constipation instead until the last when I did have diarrhea In context ↗
  • Anxiety & low moodshaky, altered mood etc In context ↗

Ask Miruvor AI

Asking aboutCrocus 40763’s story

Similar stories

  • ME/CFS with fatigue, crashes and gut symptoms, much better after faecal transplants

    Much better Coast 93315 ME/CFS Mild at worst reddit.com Oct 2026

    Coast 93315 has ME/CFS with fatigue, unrefreshing sleep and crashes after overdoing it, plus severe gut symptoms for over a decade. Long-term antibiotics helped somewhat, but faecal transplants were the single biggest difference, leaving them much better and…

  • Housebound and bedbound with ME/CFS, much better after mould avoidance and cholestyramine

    Much better Wave 67836 ME/CFS Severe at worstIll 8 years before improving or writing reddit.com Sep 2025

    At 25 in Australia he developed ME/CFS symptoms three months into a job in a mouldy building, becoming housebound and bedbound and leaving work. Mould avoidance and cholestyramine binders took him from about 20% to 60-70%, but ozone from an air purifier and…

  • ME/CFS with fatigue and brain fog, nearly back to normal after antibiotics and probiotics

    Near normal Alder 98633 ME/CFS Moderate at worstIll 8 years before improving or writing reddit.com Dec 2016

    An Australian student had gastroenteritis in India at 16, then IBS and an eight-year CFS journey with fatigue, brain fog, muscle pain and crashes after exertion. A breath test found SIBO; rifaximin and neomycin helped only briefly before symptoms returned. A…

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