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Long COVID Moderate → near normalIll 4.5 years before improving or writingNeeds ongoing treatment

Long COVID at 40% function, now nearly back to normal with time and rest

Condition
Long COVID
At worst
Moderate (mostly housebound)
Ill before improving or writing
4.5 years
Last post
Feb 2026
In their words
  • Condition: Long COVIDI had terrible depression and suicidal thoughts the first few months of my long haul. In context ↗
  • At worst: Moderatestill have days where I feel I’m only 40% where I used to be, on good days maybe 75-80%. In context ↗
  • Now: Near normalI feel like I’m still at around 90%, sometimes it goes to 80%. It varies. ... I still have neuropathy and dysautonomia.
  • Began after: COVIDI have dysautonomia post Covid so this seems to be the cause of the bladder issues for me.
Read from 86 of their posts and comments; links to the 35 this page draws on

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Summary

Owl 97945 became ill with long COVID in mid-2021, with severe anxiety and panic, suicidal thoughts, insomnia, nerve pain and dizziness, at times around 40% of her former function. She credits time and rest, with mirtazapine, propranolol and antihistamines easing sleep, heart rate and bladder symptoms. By 2023 she was about 90% and working full time; in 2026 she still had neuropathy and dysautonomia.

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What they tried

Their words about each treatment
  • L-theanine · HelpedI take the L-theanine at night mainly ... they calm me down quite well to the point that I am not panicking anymore In context ↗
  • Magnesium glycinate · HelpedMagnesium also helps me with the twitches when they're especially bad In context ↗
  • Melatonin · HelpedI find taking both of these plus L-Theanine helps me get at least 4 hours a night In context ↗
  • Meditation and breathing · Helpedif I do things to calm my nervous system (meditation/breathing) before I went to bed it seemed to happen less In context ↗
  • Electrolytes · Helpedmaking sure I'm very hydrated (not only with water but with electrolytes as well) In context ↗
  • 5-HTP · HelpedI've found that magnesium, l-theanine and 5-HTP have been helpful in getting me into at least a bit calmer state In context ↗
  • Prune juice · HelpedThis is the only thing that works for me when I'm constipated In context ↗
  • Yoga · Helpedlow impact movement like swimming, stretching and and yoga helps a bit In context ↗
  • Antibiotics for a UTI · Not saidafter I finished a round of antibiotics for a UTI In context ↗
  • Taurine · HelpedI am able to fall asleep without the jolts every night with L-Theanine magnesium glycinate, melatonin and taurine In context ↗
  • Mirtazapine · Helped a lotMirtazapine is literally the only thing that has helped my sleep during long haul In context ↗
  • Quercetin · No changeIt didn't help me In context ↗
  • Heating pad · HelpedI use the heating pad but that only does so much In context ↗
  • Propranolol · HelpedI was diagnosed with POTS and started taking propanolol which helped In context ↗
  • Stretching · HelpedLight stretching and swimming in my cold pool has helped the nerve and muscle pain, not always though In context ↗
  • Swimming in a cold pool · Helpedcold water like the pool seems to help and just laying down In context ↗
  • Rest · Helpednothing has really helped me but rest, time and antihistamines In context ↗
  • Time · Helped a lotTime is essentially the only cure In context ↗
  • Claritin (loratadine) · Helpedtaking daily antihistamines (Pepcid and Claritin) really helps In context ↗
  • Pepcid (famotidine) · HelpedI would give Claritin and Pepcid a try, it really helped me In context ↗
  • Lyrica · Not saidI also have a prescription for lyrica when the antihistamines don't help enough but I don't take it often In context ↗
  • Flu shot · No changeI did and I was fine, didn't have any reaction to it really In context ↗

Approaches: H1 antihistamines · H2 blockers · Beta-blockers · Pacing

Their path

Very severeSevereModerateMildNear normalRecovered12 mo2 y3 y4 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 2 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
mid-2021long COVID began with floaters and odd sensory reactionsMy first symptoms were floaters that did not go away In context ↗Not stated
first few monthssevere anxiety, panic, depression and suicidal thoughts, insomnia and nerve painI had terrible depression and suicidal thoughts the first few months of my long haul. In context ↗Moderate
2022-01-28improved since the beginning; about 40% on bad days, 75-80% on good daysit’s been 6 months and I’ve definitely gotten better since the beginning but still have days where I feel I’m only 40% where I used to be, on good days maybe 75-80% In context ↗MildTime and spontaneous remission
2022-01-31omicron exposure brought widespread nerve pain, twitches, brain fog and worse POTSI was doing so well prior to this and had made a lot of improvements. In context ↗Mild
2022-07-08insomnia and jerks mostly gone; anxiety and panic almost gone, POTS and pain remainingA lot better! Not 100% but the anxiety and panic symptoms have gone away almost completely, now I just deal with POTS, residual fatigue, and some muscle/nerve pain. In context ↗MildTime and spontaneous remission
2022-08-09reinfected with COVID, achy and congestedNot feeling too good right now, achy and super congested. In context ↗Mild
2022-11-07POTS much better; some days fine with no medicationI haven’t recovered but I am sooooooo much better ... some days I feel perfectly fine with no meds In context ↗Mild
2023-09-05about 90% there, working full time and active without flaresI would say I’m around 90% there. I hold down a full time job and am able to be active without having a flare up after. In context ↗Near normalTime and spontaneous remission
2026-02-16still around 90%, with lingering neuropathy and dysautonomiaI feel like I’m still at around 90%, sometimes it goes to 80%. It varies. In context ↗Near normal

Adverse events

  • Famotidine (Pepcid)“I do get anxiety from famotidine though so I take propanolol with it to help control my heart rate” In context ↗ Mood or psychiatric effects

Symptoms mentioned

Their words about their symptoms
  • Brain fogI experienced brain fog (still do sometimes) In context ↗
  • POTS & dysautonomiaI still have neuropathy and dysautonomia. In context ↗
  • Sleep problemsboth the insomnia and the jerks have gone away for the most part In context ↗
  • Pain & fibromyalgiapain that spreads all throughout my upper back and down my arms In context ↗
  • Gut problemsI had severe nausea the first 2 months of long haul, it was actually one of my first symptoms along with diarrhea but it has since subsided. In context ↗
  • Light & noise sensitivityI definitely am more sensitive emotionally and physically when it comes to stimulation or just experiencing things In context ↗
  • Heart symptoms & palpitationsVery helpful for me in controlling my heart rate and when my anxiety is out of control In context ↗
  • Muscle weaknessoccasional weakness in my extremities In context ↗
  • Neuropathy & tinglingnerve pain, tingling, electric shock type feelings, twitches and occasional weakness in my extremities In context ↗
  • Anxiety & low moodI had terrible depression and suicidal thoughts the first few months of my long haul ... I do still have the odd bout of random anxiety
  • Temperature regulationFatigue, nerve pain in arms and legs, twitches, POTS, hot flashes In context ↗
  • Vision problemsmy vision is now clear with the glasses when it used to be blurry even with my glasses In context ↗

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