Miruvor
Sign up
Long COVID Severe → much betterIll 2.5 years before improving or writing

Sometimes bedbound with long COVID and too weak to talk, now much better

Condition
Long COVID
At worst
Severe (mostly bedbound)
Ill before improving or writing
2.5 years
Last post
Jan 2026
In their words
  • Condition: Long COVIDI got Covid on July 14,’23 and it was just a cold. In context ↗
  • At worst: Severe5 days later I crashed severely I could barely talk because I was so weak and felt head was on fire In context ↗
  • Now: Much betterI am much improved probably 80% now ... I am still not back to work yet In context ↗
  • Began after: COVIDI got Covid on July 14,’23 and it was just a cold. In context ↗
Read from 36 of their posts and comments; links to the 21 this page draws on

Request to remove this story

Summary

A 35-year-old woman became ill with long COVID after a mild July 2023 infection and five days later crashed, too weak to talk; she lost her job and was sometimes bedbound. A bad cold that October brought the symptoms back. She improved slowly over two and a half years, though a stellate ganglion block in 2024 left her worse for weeks and she doubted it was worth it; fatigue, brain fog and tachycardia remained.

Ask Miruvor AI

Asking aboutZephyr 47571’s story

What they tried

Their words about each treatment
  • buspirone · WorseI had the zaps from taking buspirone. It was the weirdest feeling. I didn’t like the feeling so I stopped the meds and the zapping stopped too In context ↗
  • 24 hour fast · WorseI tried it, it made me feel so much worse. I need to feed myself every few hours In context ↗
  • gabapentin · Helpedit helps me sleep at night, I don’t have any other odd side effects from it, and it helps with my back pain and headaches In context ↗
  • LDN · WorseI tried LDN A few weeks ago. It made my symptoms worse, fatigue, brain fog etc. I tried pushing through but I couldn’t do it. And it was .5mg. In context ↗
  • Wellbutrin · WorseUnfortunately that was worse, I only took it for 4 days maybe? Felt so horrible I couldn’t do it. In context ↗
  • Breaking Free by Jan Rothney · No changeI did Jan rothneys course which was very informative but I didn’t really find much improvement in my recovery. In context ↗
  • SGB · WorseI felt worse for a few weeks honestly. Then it settled and I very very slowly started getting better In context ↗
  • EAT (Epipharyngeal Abrasive Therapy) · HelpedThe eat did well for me I think. He said it was swollen but only grade 1. I didn’t even realize how congested I was until after I can breathe so much better now. In context ↗
  • beta blockers · HelpedI was on beta blockers, I think it helped because I rarely get it anymore. But they had horrible side effects. In context ↗
  • meditation · HelpedI laid down every day and listened to something that I enjoyed, whether a podcast, meditation, nature sounds In context ↗
  • somatic tracking · HelpedI also did somatic tracking, a bit of eft, not to get rid of the symptoms but to get in tune with my body and calm my system. In context ↗
  • pacing · HelpedI still have some bad days for sure because my pacing habits are bad sometimes In context ↗

Approaches: Brain retraining · Mind-body practices · Trauma & somatic work

Their path

Very severeSevereModerateMildNear normalRecoveredonset6 mo12 mo18 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. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they were
July 14, 2023mild COVID-19 infectionI got Covid on July 14,’23 and it was just a cold. In context ↗Mild
July 19, 2023severe crash five days after infection5 days later I crashed severely I could barely talk because I was so weak and felt head was on fire. In context ↗Severe
October 2023slow improvementI am definitely improving from what I was 2 months ago! In context ↗Moderate
October 2023crashed after a bad cold/fluthen bam I got a bad cold/flu a few weeks ago and the symptoms came back, but I am slowly improving again In context ↗Moderate
February 2024slow up-and-down improvement, short walks a few times a weekSome days I am still housebound and some days bed bound. I can now take slow walks usually a few times a week. It’s up and down a lot. In context ↗Moderate
July-August 2024felt worse for weeks after stellate ganglion block and EAT in DallasAnd I felt worse for a few weeks honestly. In context ↗Moderate
December 2024head pressure and vertigo mostly gone, brain fog and fatigue leftMy head pressure is 90% gone In context ↗Moderate
May 2025doing much better, not back at work, tachycardia remainsI am doing so much better than I was back then but def not 100% yet and not back to work yet. In context ↗Mild
January 2026about 80% improved, still not back at workI am much improved probably 80% now. ... I am still not back to work yet. In context ↗Mild

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseNow I just have fatigue, pem, head pressure In context ↗
  • Brain fogStill have some brain fog and fatigue tho In context ↗
  • POTS & dysautonomiaSymptoms 95% gone: vertigo, lethargy, nightmares, tinnitus, head pressure, bad sleep, palpitations. In context ↗
  • Headaches & migraineI had head pressure for a long time too, almost 2 years. In context ↗
  • Sleep problemsI can’t sleep more than 7-8 hours. In context ↗
  • BreathlessnessI can breathe so much better now In context ↗
  • Heart symptoms & palpitationsSymptoms remaining: some fatigue and brain fog, tachycardia. ( taking beta blockers for that) In context ↗
  • Muscle weaknessI could barely talk because I was so weak In context ↗
  • Anxiety & low moodIt’s really tough and now my mental health is really bad. In context ↗
  • Flu-like symptomsThe fever flu stuff hasn’t happened for a few months. In context ↗
  • Pain & fibromyalgiait helps with my back pain and headaches. In context ↗

Ask Miruvor AI

Asking aboutZephyr 47571’s story

Similar stories

  • Bedbound for months with ME/CFS, now somewhat better with pacing and guanfacine

    Somewhat better Kite 77342 ME/CFS Severe at worstIll 16 months before improving or writing reddit.com Oct 2026

    Kite 77342 got EBV in June 2025 and later spent months bedbound in a dark room with severe brain fog, light and sound sensitivity and around 700 steps a day at worst. Pacing, nervous-system work and guanfacine from February 2026 brought slow, uneven…

  • Bedbound with long COVID, now recovered after olanzapine and brain retraining

    Recovered Petrel 21036 Long COVID Very severe at worstIll 1 year before improving or writing reddit.com Oct 2026

    An Australian woman caught COVID in May 2023 and deteriorated over six months until she was bedbound, in rolling PEM, and hospitalised for three weeks. She credits olanzapine, zinc and brain retraining (Primal Trust, then the Lightning Process) for a full…

  • Very severe ME/CFS after COVID, unable to sit up, now much better with EMDR and meditation

    Much better Canyon 91824 ME/CFS Very severe at worstIll 28 years before improving or writing reddit.com Oct 2026

    Ill since Lyme disease at age 12, diagnosed with ME/CFS at 25, she drifted between moderate and severe, improving to upper-mild by early 2025. COVID in August 2025 left her very severe, unable to sit up, see or tolerate light for months. From March 2026 she…

  • Couchbound with long COVID, now nearly back to normal after mind-body work and sleep meds

    Near normal Beech 14076 Long COVID Severe at worstIll 2 years before improving or writing reddit.com Oct 2026

    A counselor developed long COVID in February 2024 with MCAS-like reactions, POTS, insomnia, brain fog and anxiety; she was couchbound and took four months off work. She credits mind-body and trauma work (IFS, somatic experiencing, brainspotting), meditation…

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