Miruvor
Sign up
Long COVID Severe → much betterIll 4 years before improving or writingNeeds ongoing treatment

Unable to walk with long COVID, now much better after salt and compression stockings

Condition
Long COVID
At worst
Severe (mostly bedbound)
Ill before improving or writing
4 years
Last post
Feb 2024
In their words
  • Condition: Long COVIDI have had LC for 15 months now. Mainly POTS symptoms. In context ↗
  • At worst: SevereI had severe weakness in my legs, couldn’t walk for about 3 months In context ↗
  • Now: Much betterI was able to get back at about 80% ... down for a week or so and nothing more
  • Began after: COVIDHad COVID twice. First was in 2020 and that was before vaccine and it was horrible.
Read from 21 of their posts and comments; links to the 12 this page draws on

Request to remove this story

Summary

Fell ill with COVID in 2020 and could not walk for about three months; she improved over six to eight months. A July 2022 reinfection was followed by night-time tachycardia up to 175bpm starting in November, ER trips, a later POTS diagnosis and leg pain. Beta blockers were intolerable with low blood pressure, so she used salt, fluids and compression stockings, reaching about 80% by December 2023 before another reinfection; by February 2024 she was walking more.

Ask Miruvor AI

Asking aboutSwan 76577’s story

What they tried

Their words about each treatment
  • beta blockers (bisoprolol) · WorseI am on it for SVT and it’s causing me a bit of shortness of breath, dizziness and body pains. In context ↗
  • salt, fluids and electrolytes · Helped a lotMake sure you get lots of liquid and salt. Only thing that have helped me tremendously. In context ↗
  • walking · HelpedI have been pushing myself to walk and workout more and felt that I was doing much better In context ↗
  • magnesium · HelpedLots of salt, magnesium and electrolytes help. In context ↗
  • compression stockings · HelpedI wear the compressions stockings although I hate them so much but they do help a bit with the pain. In context ↗
  • B12 · Not saidI was taking B12 up to January when I was hospitalized after having severe bouts of tachycardia and once I had blood test my b12 was high so I stopped since. In context ↗

Approaches: POTS medication · Exercise and activity

Their path

Very severeSevereModerateMildNear normalRecoveredonset12 mo2 y3 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. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they were
2020First COVID-19 infection; severe leg weakness, could not walk for about three months, vision problemsI had severe weakness in my legs, couldn’t walk for about 3 months In context ↗Severe
six to eight months latergradual recovery, left with palpitations, dizziness and eye floatersit took me about 6-8 month to get better In context ↗Mild
November 2022extreme night-time tachycardia up to 175bpm, ER visits, daily dizziness, leg weakness and painI started experiencing extreme Tachycardia at night when sleeping. In context ↗Moderate
September 2023other symptoms better, still tachycardia and daily palpitationsOther symptoms got better. In context ↗Mild
December 2023back to about 80% of normalI was able to get back at about 80% In context ↗Mild
December 2023COVID reinfection caught from child's schoolcaught COVID from my kid’s school a few days ago :( In context ↗Mild
February 2024pushing herself to walk and work out more; still awaiting a POTS specialistI have been pushing myself to walk and workout more and felt that I was doing much better In context ↗Mild

Adverse events

Symptoms mentioned

Their words about their symptoms
  • POTS & dysautonomiaI was diagnosed with POTS after having COVID. In context ↗
  • Pain & fibromyalgiaYes, my legs hurts all the time. In context ↗
  • Muscle weaknessI had severe weakness in my legs In context ↗
  • Headaches & migraineI have mostly head pressure/pain, weakness and congestion. In context ↗
  • Gut problemsLike headache, nausea, fever.. In context ↗
  • Vision problemslots of vision issue In context ↗
  • Anxiety & low moodI am so lost and depressed:( In context ↗
  • Post-exertional malaiseI’m also scared of going and over exhausting my body and then have worst LC. In context ↗

Ask Miruvor AI

Asking aboutSwan 76577’s story

Similar stories

  • Not enough detail to draw a path

    Often bedridden with long COVID, pacing helped, then stress and reinfection brought relapse

    Relapsed Harbor 76223 Long COVID Severe at worstIll 6 years before improving or writing reddit.com Oct 2026

    She developed long COVID in December 2020 and spent six years often bedridden with PEM, brain fog, air hunger, POTS and loss of smell, plus heavy uterine bleeding needing transfusions and a hysterectomy. By summer 2026 she was swimming and walking laps in…

  • Long COVID too faint to walk or drive, now good most days at about 80-85%

    Much better Grove 43730 Long COVID Moderate at worstIll 6 months before improving or writing reddit.com Oct 2026

    A woman who fell ill with long COVID in August 2023 was too faint to walk around much or drive, with brain fog, breathlessness and anxiety. Quitting her job and resting six months, plus supplements, brought her to about 90% by mid-2024, but a January 2025…

  • 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…

  • Housebound with long COVID for about two years, now about 15% better with rest and fluids

    Somewhat better Kite 24968 Long COVID Severe at worstIll 4.5 years before improving or writing reddit.com Oct 2026

    They caught COVID in January 2022 during a hospital stay and developed long COVID that March, losing their job and spending about two years housebound. They put themselves roughly 15% better than 2022, crediting rest and fluids, with cool showers making…

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