Miruvor
Sign up
Long COVID RelapsedIll 2.5 years before improving or writing

Long COVID with POTS and fatigue, improved for 18 months then relapsed

Condition
Long COVID
At worst
Not stated
Ill before improving or writing
2.5 years
Last post
Aug 2024
In their words
  • Condition: Long COVIDI had covid 3 x in 2022; Jan, Aug, Nov and ended up with POTs In context ↗
  • Now: Relapsed18 months of rarely thinking about it. ... Got really stressed and then a bad virus in june/july 2024 (Australian winter) and the POTs is back in all it’s ridiculous and life altering ways. In context ↗
  • Began after: COVIDI had covid 3 x in 2022; Jan, Aug, Nov and ended up with POTs In context ↗
Read from 5 of their posts and comments; links to the 4 this page draws on

Request to remove this story

Summary

Alpine 97110 caught covid three times in 2022 and developed POTS and post-viral fatigue. By January 2023 antihistamines, rest, electrolytes, vitamin C IVs, B12 and minerals had them living life again for about 18 months. A bad virus after stress in mid-2024 brought the POTS back, and by August 2024 they were still stuck with fatigue, weakness, nausea, brain fog and low mood.

Ask Miruvor AI

Asking aboutAlpine 97110’s story

What they tried

Also tried

gentle work to regulate the vagus nerve· Not said
Their words about each treatment
  • Antihistamines · Helped a lotAntihistamines got me out of it last time, along with rest, electrolytes, IVs of Vit C, B12 injections and replacing minerals. In context ↗
  • somatic therapy · Helped a lotI second somatic therapy. ... It made such a difference for me that I went and studied it myself. In context ↗
  • gentle work to regulate the vagus nerve · Not saidDoing gentle work to regulate it again In context ↗

Approaches: H1 antihistamines · POTS medication · Pacing · Supplements · Trauma & somatic work

Their path

Very severeSevereModerateMildNear normalRecovered12 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 10 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
Jan 2022First of three covid infections in 2022; developed POTSI had covid 3 x in 2022; Jan, Aug, Nov and ended up with POTs In context ↗Not stated
Nov 2022Lowest point after three covid bouts in 2022after the hell that was 3 bouts of covid in 2022 In context ↗Moderate
Jan 2023Back to living life again for about 18 monthsHowever by Jan 2023 I was pretty good and living life again. ... 18 months of rarely thinking about it. In context ↗Near normalH1 antihistamines (unspecified)
June/July 2024POTS came back after stress and a bad virusGot really stressed and then a bad virus in june/july 2024 (Australian winter) and the POTs is back in all it’s ridiculous and life altering ways. In context ↗Moderate
2024-08-12Still stuck in post-viral fatigue, nausea, brain fog and low mood two months after the virusI’m still stuck in post viral fatigue, weakness, nausea, brain fog, and anxiety/sadness. In context ↗Moderate

Symptoms mentioned

Their words about their symptoms
  • POTS & dysautonomiathe POTs is back in all it’s ridiculous and life altering ways In context ↗
  • Brain fogI’m still stuck in post viral fatigue, weakness, nausea, brain fog, and anxiety/sadness. In context ↗
  • Anxiety & low moodbrain fog, and anxiety/sadness In context ↗
  • Gut problemsI have months of fatigue, neuroinflammation and nausea. In context ↗
  • Muscle weaknessI’m still stuck in post viral fatigue, weakness, nausea In context ↗

Ask Miruvor AI

Asking aboutAlpine 97110’s story

Similar stories

  • Long COVID with heart, lung and nerve damage, now somewhat better; water fast helped

    Somewhat better Plover 62455 Long COVID Severe at worstIll 5 years before improving or writing reddit.com Oct 2026

    Plover 62455 developed long COVID in early 2021 after a second infection in late 2020, accumulating heart, lung and nervous system damage, dysautonomia, MCAS and fibromyalgia. She reached near-total remission twice, once after a water fast, each lasting…

  • Couch-ridden with long COVID, now much better after strict diets and a faecal transplant

    Much better Starling 72647 Long COVID Severe at worst reddit.com May 2024

    They fell ill with mononucleosis around 2015, were worst in 2017, and had recovered to about 80 percent when COVID in spring 2020 knocked them back down. They credit strict diets with lifting them from couch-ridden to working and hiking, with naturopathic…

  • Bedbound and housebound with ME/CFS, now much better with pacing and POTS/MCAS drugs

    Much better Orchid 39721 ME/CFS Very severe at worstIll 28 years before improving or writing reddit.com Oct 2026

    Diana fell ill at 12 in 1998 and was very severe for about 15 years, bedbound for about four years and housebound for another seven or so. Endometriosis surgery moved them to moderate, and treating POTS and MCAS from late 2024 brought them toward mild.…

  • 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…

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