Miruvor
Sign up
Long COVID Moderate → much betterIll 3 years before improving or writingNeeds ongoing treatment

Long COVID with POTS and neuropathy, much better after IgG food cuts and rosuvastatin

Condition
Long COVID
At worst
Moderate (mostly housebound)
Ill before improving or writing
3 years
Last post
Oct 2026
In their words
  • Condition: Long COVIDI'm kinda new to relating my POTS/MCAS/Neuropathy to post-vaccine injury In context ↗
  • At worst: ModerateI stay home, do not go out unless totally necessary and mask when I do. In context ↗
  • Now: Much betterSO many things are better, like I can drive and sleep but the shakes are embarrassing In context ↗
  • Began after: a vaccinationgot all my COVID vaccines and boosters and wham In context ↗
Read from 13 of their posts and comments; links to the 11 this page draws on

Request to remove this story

Summary

After COVID vaccinations and a course of nitrofurantoin they believe they developed POTS, MCAS and neuropathy, stayed home a lot and ate a low-histamine diet with antihistamines. POTS eased after about six months, then returned after influenza A in early 2025. Cutting out nearly all IgG-flagged foods and starting rosuvastatin left them much better, though tremors and a lost singing voice remained.

Ask Miruvor AI

Asking aboutCardinal 54328’s story

What they tried

Their words about each treatment
  • cleaning every day for months · HelpedI had no choice except to clean every day for months. I felt better. In context ↗
  • low histamine diet · HelpedMy symptoms slllloooooooooowly improved over a year being on a "mostly" low histamine diet In context ↗
  • antihistamines · Not saidI stay on a low histamine diet with antihistamines In context ↗
  • beta blockers · WorseI tried two beta blockers-one gave me extreme fatigue and the other very itchy lungs. In context ↗
  • rosuvastatin · Helped a lotI also was recently put on a statin (rosuvastatin) and suddenly felt MUCH better. In context ↗
  • IgG-guided food elimination · Helped a lotI gave up all but 1 (chocolate) and felt SO MUCH better-I mean mentally and physically. In context ↗
  • probiotics · Helpedbuilding back I can see how much probiotics are helping In context ↗
  • doing nothing til March · Not saidSo I am literally doing NOTHING til March. In context ↗
  • COVID vaccination as treatment · Not saidgot all my COVID vaccines and boosters and wham In context ↗

Approaches: Diet · Exercise and activity · Statins · Supplements

Their path

Very severeSevereModerateMildNear normalRecovered6 mo12 mo18 mo2 y2.5 y

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. The chart starts 6 months after onset: the story doesn’t say how ill they were before that. 1 step says too little to place on the scale and is only in the table. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
onsetPOTS and MCAS began after COVID vaccination and a course of nitrofurantoinI got POTS/MCAS after I believe vaccine and a round of Nitrofurantoin In context ↗Not stated
after about 6 monthsPOTS began to subside on a low-histamine diet with antihistamines, neuropathy did notAfter about 6 months, my POTS began to subside, I stay on a low histamine diet with antihistamines, but my neuropathy is NOT subsiding In context ↗ModerateLow-histamine diet
late Jan 2025influenza A for a month, POTS came back; stayed home a lotI caught Influenza A in late Jan and I was sick for the entire month of Feb In context ↗Moderate
January 2026cut out all IgG-flagged foods and started rosuvastatin; felt much betterI gave up all but 1 (chocolate) and felt SO MUCH better ... I also was recently put on a statin (rosuvastatin) and suddenly felt MUCH better In context ↗MildElimination diets (other)
July 2026could drive and sleep again, tremors and lost voice remainedSO many things are better, like I can drive and sleep but the shakes are embarrassing and I'm hoping to start teaching crafting classes soon In context ↗Mild
October 2026better after three years of MCAS and POTSI had MCAS/POTS for 3 years-am better now In context ↗Mild

Adverse events

Symptoms mentioned

Their words about their symptoms
  • POTS & dysautonomiaAfter about 6 months, my POTS began to subside In context ↗
  • Mast cell (MCAS) & allergiesI had MCAS/POTS for 3 years-am better now In context ↗
  • Neuropathy & tinglingmy neuropathy is NOT subsiding, which is scary In context ↗
  • Sleep problemsSO many things are better, like I can drive and sleep In context ↗

Ask Miruvor AI

Asking aboutCardinal 54328’s story

Similar stories

  • Long COVID with brain fog, pain and fatigue, now much better on antihistamines and diet

    Much better Flint 72776 Long COVID Moderate at worstIll 4 years before improving or writing reddit.com Oct 2026

    After a mild 2020 COVID infection and near-complete recovery, an Italian man in his early 40s dates his disabling illness to a Pfizer dose in June 2021, which he says left him disabled for years with brain fog, gut problems, pain and fatigue. From 2025 he…

  • Almost bedbound with long COVID, now nearly back to normal after diet and pacing

    Near normal Sequoia 24448 Long COVID Severe at worstIll 2.5 years before improving or writing reddit.com Oct 2026

    Sequoia 24448, a man under 30, developed long COVID after a third infection in February 2024 and at his worst was almost bedbound with gut, skin, nerve and cognitive symptoms. A low-histamine, gluten- and dairy-free diet, supplements, probiotics, pacing,…

  • Long COVID with brain fog and POTS, now 85-90% of normal after supplements and pacing

    Near normal Dew 68600 Long COVID Mild at worstIll 2 years before improving or writing reddit.com Oct 2026

    A Dutch student and chef who fell ill with long COVID in 2021, with brain fog, PEM, POTS, headaches and histamine reactions, and had to stop school. He credited supplements — NAC, quercetin, vitamin D, magnesium taurate, vitamin C, salt and electrolytes —…

  • Long COVID, barely able to do anything, nearly back to normal after time and rest

    Near normal Rain 52033 Long COVID Moderate at worstIll 2 years before improving or writing reddit.com Sep 2026

    Rain 52033 caught COVID-19 in March 2020 and could do very little for about five months, with dizziness, nerve pain, breathlessness, gut trouble and brain fog. They credit time, rest, sleep, nutrition and gentle walking, plus smaller gains from famotidine,…

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