Miruvor
Sign up
Long COVID Severe → near normalIll 2 years before improving or writingNeeds ongoing treatment

Couch-bound with long COVID, now about 95% of baseline after rehab and compression

Condition
Long COVID
At worst
Severe (mostly bedbound)
Ill before improving or writing
2 years
Last post
May 2024
In their words
  • Condition: Long COVIDChest burning pain and tightness is my new symptom since having long covid for 6 months In context ↗
  • At worst: SevereCouldn’t get off my couch for months. Didn’t want to live like that. In context ↗
  • Now: Near normalim 95 percent back to baseline In context ↗
  • Began after: COVIDI was given Paxlovid my second covid infection in may 22 and it made me feel worse and LC started immediately following. In context ↗
Read from 25 of their posts and comments; links to the 11 this page draws on

Request to remove this story

Summary

A golfer, she recovered from COVID in January 2021, but a December 2021 booster and a second infection in May 2022, worsened by Paxlovid, brought long COVID. Couch-bound for months with chest pain, a standing heart rate of 135, brain fog and heat intolerance, she was diagnosed with POTS. A customised aerobic and strength rehab programme, compression and sodium brought her to about 95% of baseline by May 2024, with gut symptoms and dizziness left.

Ask Miruvor AI

Asking aboutPrairie 48131’s story

What they tried

Also tried

Their words about each treatment
  • Bactrim · Much worseI ended up in ER after being prescribed Bactrim for a UTI! In context ↗
  • cipro · WorseI too add cipro along with all sulfa antibiotics as my allergy list. In context ↗
  • inhaler · Helpedthe doc put me on an inhaler b/c I have seasonal allergies and he said this could be a post viral asthma… it has helped In context ↗
  • compression socks/leggings; hydration with added sodium; head of bed raised · HelpedThose all have helped me ... not dramatically but better than without. In context ↗
  • LDN · Not saidShe got me off LDN and mestinon. No drugs currently. In context ↗
  • personalized POTS exercise rehab program (riseabovepots PT) · Helped a lotI found a physical therapist that was able to help treat and get my pots in remission through a customized aerobic and strength training, rehab program In context ↗
  • Dr Sabine Hazan gut health protocol · Helped a lotIt has been working wonders for me… anxiety has disappeared. In context ↗
  • COVID vaccination as treatment · Not saidI had bad reaction to my covid third shot in dec ‘21… never putting mrna in my body ever again. In context ↗

Approaches: POTS medication · Physiotherapy and rehab

Their path

Very severeSevereModerateMildNear normalRecovered18 mo21 mo2 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 first step with a time is 17 months after onset: the story doesn’t say how ill they were before that. The dashed part: the story doesn’t say when. 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
May 2022second COVID infection, Paxlovid, long COVID beganI was given Paxlovid my second covid infection in may 22 and it made me feel worse and LC started immediately following. In context ↗Not stated
2022couch-bound for months, competitive golf sidelinedCouldn’t get off my couch for months. In context ↗Severe
October 2023able to walk an hour a day, still limitedhave not been able to do much more than walk an hour a day In context ↗Mild
April 2024POTS diagnosed; POTS rehab programmeI am hitting just over 2 years and 85% better once i got better diagnosis of POTs. In context ↗MildGraded rehab and self-made programmes
May 202495% back to baselineBut yeah im 95 percent back to baseline. In context ↗Near normal

Adverse events

Symptoms mentioned

Their words about their symptoms
  • POTS & dysautonomiaMy HR would go from 70 to 135 in less than 2 mins from lying down/sitting to standing up. In context ↗
  • Heart symptoms & palpitationsChest discomfort was worst symptom. In context ↗
  • Brain fogfatigue, brain fog, chest pain/discomfort, dizziness all gone In context ↗
  • Breathlessnessshortness of breath etc etc all were my symptoms and all are gone In context ↗
  • Anxiety & low moodI had two weeks of dissociative feelings and terrible anxiety for quite awhile….. all gone now. In context ↗
  • Temperature regulationHeat intolerance was terrible In context ↗
  • Gut problemsmy gastro symptoms still not fully recovered In context ↗

Ask Miruvor AI

Asking aboutPrairie 48131’s story

Similar stories

  • Long COVID at 25% function at worst, now much better after treating migraine and POTS

    Much better Otter 89676 Long COVID Severe at worst reddit.com Oct 2026

    A bad virus in 2018 led to ME/CFS; Covid in 2020 took them from mild to moderate-severe, and after a booster in early 2022 migraines became daily and at worst they were largely in a dark room at about 25% function. Treating migraine, POTS and MCAS helped; by…

  • Not enough detail to draw a path

    Neuro long COVID with dizziness and brain fog, now close to normal after rest and pacing

    Near normal Alder 85142 Long COVID Moderate at worstIll 7 months before improving or writing reddit.com Oct 2026

    A woman in her thirties in Germany developed neuro long COVID after a first COVID infection in 2024, with dizziness, brain fog and headaches. She credits radical rest, pacing and a three-month break from work; a first Novavax shot helped clear the last…

  • Long COVID with brain fog and POTS, now around 90% of normal after rest and saunas

    Near normal Tide 94699 Long COVID Severe at worstIll 10 months before improving or writing reddit.com Oct 2026

    Tide 94699 caught COVID in March 2024 and spent the first months sleeping day and night, with brain fog, POTS, headaches and GI and vision problems. Rest, daily saunas, antihistamines, nicotine patches and gradually longer walks were credited as things…

  • Almost bedbound with long COVID, now much better on ivabradine

    Much better Lake 77945 Long COVID Severe at worstIll 20 months before improving or writing reddit.com Oct 2026

    A man of 30 developed long COVID in August 2023 with POTS, breathlessness, nerve pain, brain fog and PEM; pushing through work and grad school left him almost bed-bound at 20% of capacity. Kefir, LDN and pacing gave partial gains, but ivabradine from April…

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