Miruvor
Sign up
Long COVID Moderate → much betterIll 6.5 years before improving or writing

Unable to work with long COVID, now much better after duloxetine and pacing

Condition
Long COVID
At worst
Moderate (mostly housebound)
Ill before improving or writing
6.5 years
Last post
Sep 2026
In their words
  • Condition: Long COVIDI got LC during my second year of grad school. I knew something was wrong because the bottom fell out and I couldn't do any work. In context ↗
  • At worst: Moderatethe bottom fell out and I couldn't do any work ... Took me 1+ years to submit my thesis In context ↗
  • Now: Much betterI'm looking at PhDs now that I'm recovered a bit more and the fog is better In context ↗
  • Began after: COVIDI got LC during my second year of grad school.
Read from 33 of their posts and comments; links to the 22 this page draws on

Request to remove this story

Summary

Trail 10686 fell ill with long COVID in February 2020 during grad school, unable to work and taking over a year to finish a thesis through brain fog. Duloxetine for nerve pain kickstarted a partial recovery, with later gains from 5-HTP, pacing, acupuncture and TMS. They still have POTS, pain and GERD with slow post-exertional recovery, calling themselves better but not functioning.

Ask Miruvor AI

Asking aboutTrail 10686’s story

What they tried

Their words about each treatment
  • Cymbalta (duloxetine) · Helped a lotCymbalta kickstarted my recovery, but my pots symptoms became more prominent In context ↗
  • Lyrica (pregabalin) · Not saidMy LC Dr recommended lyrica and cymbalta. ... I can only take it at night bc it throws off my POTS In context ↗
  • Medical cannabis (CBD, CBG, CBC, CBN) · Helpedit helps me stay off other painkillers and improves my mood esp when stuck in bed In context ↗
  • CPAP · Not saidI also then got a CPAP but I no longer have it In context ↗
  • Compression socks (Sockwell) · Not saidi got some sockwells recently that I like. bamboo and wool In context ↗
  • 5-HTP · HelpedMy dr recommended 5-htp and it cleared up some brain fog for me. In context ↗
  • Benadryl · Not saidsaw this on the sub and started taking it as well. Havent tried in the day but next day I notice if have taken it or not In context ↗
  • tryptophan · HelpedStarted treating that with 5-htp and tryptophan and that helped. In context ↗
  • Pacing · HelpedSpoons helps a bit. You have to learn to stop activity before you threshold In context ↗
  • Swimming · Not saidswimming seems to keep HR low since water compresses/cools. In context ↗
  • Acupuncture · HelpedI just got acupuncture on that area and it REALLY helped. In context ↗
  • Neck roll pillow and cervical massager · HelpedI got a neck roll pillow and a cervical neck stretch/massager. Also really helps In context ↗
  • Chia seeds · Helpedthe biggest thing I noticed that helped me is chia seeds In context ↗
  • COVID vaccination (5th dose, 2023) · Helpedafter my most recent (‘23) one I got significantly better after the usual flare it caused In context ↗
  • Diabetic diet · Helpedmy pots mimic diabetes. A diabetic diet helps In context ↗
  • Electrolytes and salt water · HelpedI found my GERD is helped by drinking more saltwater ( I do for POTS). In context ↗
  • TMS · Helpedthey added an anxiety protocol to address long Covid specifically. It’s helped, and less downsides compared to starting a new med. In context ↗
  • Pain psychology intervention · HelpedI was presented with this kinda stuff in a pain psychology intervention and it’s helped me realize where my brain and body aren’t communicating well. In context ↗

Approaches: SNRIs · Brain stimulation · Supplements · Vaccination

Their path

Very severeSevereModerateMildNear normalRecoveredonset12 mo2 y3 y4 y5 y6 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 wereAfter
Feb 2020Long COVID began during grad schoolI got LC during my second year of grad school. I knew something was wrong because the bottom fell out and I couldn’t do any work. In context ↗Moderate
2020-2021Could not work; over a year to submit thesis through brain fogTook me 1+ years to submit my thesis, I’d have to rewrite things constantly because I would forget where I was. In context ↗Moderate
2024-02Duloxetine for nerve pain started recoveryCymbalta kickstarted my recovery, but my pots symptoms became more prominent In context ↗MildDuloxetine (Cymbalta)
2025Brain fog cleared with meds and pacingbrain fog went away with meds and pacing In context ↗MildPacing and the energy envelope
2026-03TMS and ivabradine brought further gainsIt’s definitely weird, but it’s been shockingly good! In context ↗MildrTMS (transcranial magnetic stimulation)
2026-09-28Still limited by physical symptomsI’ve also gotten a fuck ton of treatment for my physical symptoms and meds are what started *some* recovery. In context ↗Mild

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI get concussion like symptoms from overdoing it. In context ↗
  • Brain fogbrain fog went away with meds and pacing In context ↗
  • POTS & dysautonomiaCymbalta kickstarted my recovery, but my pots symptoms became more prominent In context ↗
  • Pain & fibromyalgiaMy LC made my fibro/pots debilitating. In context ↗
  • Neuropathy & tinglingWith those both treated, good improvement in neuro pain In context ↗
  • Heart symptoms & palpitationsI had HR spikes of 60+ when starting exercise which would level out. In context ↗
  • Anxiety & low moodI’m on week 3 of TMS for depression (existing pre COVID) In context ↗
  • Gut problemsI found my GERD is helped by drinking more saltwater In context ↗
  • Muscle weaknessI also have a weak neck, so I have a lot of coathanger pain and shoulder tension In context ↗

Ask Miruvor AI

Asking aboutTrail 10686’s story

Similar stories

  • Mild ME/CFS while working full time, somewhat better after prolotherapy

    Somewhat better Glacier 34729 ME/CFS Mild at worstIll 10 years before improving or writing reddit.com Oct 2026

    Around 2011 she developed mild CFS and kept working full time despite pain. Low-dose naltrexone, Cymbalta, testosterone, qi gong, yoga, massage and chiropractic made it more bearable. She suspected mild cervical instability and had prolotherapy on her neck,…

  • Bed-bound with long COVID, improved on mestinon then relapsed, unable to work full-time

    Relapsed Island 22899 Long COVID Very severe at worstIll 7 months before improving or writing reddit.com Jul 2026

    A US designer and former distance runner, she fell ill in March 2020 and by late 2020 was largely bed-bound with post-viral POTS and small fibre neuropathy, needing help getting out of the shower. Mestinon, salt, compression socks, exercise and two Pfizer…

  • Long COVID severe brain fog and POTS, improved then relapsed, crediting rest and vaccines

    Relapsed Ridge 89426 Long COVID Severe at worstIll 13 months before improving or writing reddit.com Apr 2026

    A public defender who caught COVID in December 2020 and spent months with severe brain fog, PEM, POTS and lost taste and smell, hospitalised for a week with tachycardia in mid-2021. She credits rest, time off work and the COVID vaccines, which restored her…

  • Long COVID with suicidal ideation; LDN and lithium helped, then reinfection set them back

    Relapsed Badger 90833 Long COVID Severe at worstIll 6 years before improving or writing reddit.com Mar 2026

    Caught COVID in January 2020, was long-hauling for almost three years with suicidal ideation, and improved somewhat on low-dose naltrexone and low-dose lithium, though a second infection in May 2022 worsened symptoms and they remained at about 50% recovered.

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