Miruvor
Sign up
Long COVID Moderate → somewhat betterIll 6 years before improving or writingNeeds ongoing treatment

Long COVID with pain, neuropathy and brain fog, somewhat better with Bactrim and Adderall

Condition
Long COVID
At worst
Moderate (mostly housebound)
Ill before improving or writing
6 years
Last post
Apr 2026
In their words
  • Condition: Long COVIDI got long Covid in Feb 2020-so coming up on 4 years. In context ↗
  • At worst: ModerateI had all kinds of really severe neurological issues in the summer of 2024 and I was unable to drive for about three months. In context ↗
  • Now: Somewhat betterThe only things that have made this bearable are Adderall and Bactrim. In context ↗
  • Began after: COVIDMy first exposure that I got long Covid, I was asymptomatic.
Read from 20 of their posts and comments; links to the 15 this page draws on

Request to remove this story

Summary

Long COVID began in February 2020, after an asymptomatic COVID infection in January 2020. Six years on, chest and nerve pain, neuropathy, insomnia, brain fog, depression and MCAS symptoms continued to flare with each COVID exposure. Bactrim and Adderall were credited with making life bearable, and Vive Minerals restored taste and smell in late 2023. They remained ill and disabled.

Ask Miruvor AI

Asking aboutFox 33206’s story

What they tried

Their words about each treatment
  • antibiotics for Lyme · No changeafter trying years of antibiotics and all kinds of supplements In context ↗
  • Adderall · Helped a lotThe Adderall improves mood immensely. ... it gives me a positive mood, energy, a desire to do things when I would otherwise be in bed crying. In context ↗
  • Bactrim (sulfamethoxazole) · Helped a lotThe only thing that worked- and works AMAZING to kill the pain- is Bactrim- or sulfamethoxazole. In context ↗
  • IV vitamin C and B · Helped a lotI did five weeks IV vitamin C therapy for Epstein bar virus ... A month later, they all came back In context ↗
  • Paxlovid · Helped a lotIt was freaking amazing. I had so many wonderful positive effects ! ... The bad news is that it is starting to come back now- at least some of the symptoms are. In context ↗
  • Alpha Lipoic acid · HelpedAlpha Lipoic acid gets RID of my peripheral neuropathy!!! I love it. I have to take 2 pills 3x a day- it starts coming back after the pills wear off in a few hours In context ↗
  • Vive Minerals · Helped a lotWithin a few days of taking it, I noticed my taste coming back. Within less than a week AAALLL my taste and smell was back! In context ↗
  • methylated B12 · HelpedI think mostly methylated B12 wa a big help - a form that dissolves under the tongue. In context ↗
  • B1 · Not saidAnd B1, some B6 pulsed on and off In context ↗
  • powdered L- glutamine · HelpedI did begin taking powdered L- glutamine a few months ago to heal my gut. It did not necessarily fix my mental health issues , but it has worked great in the past for gut issues In context ↗
  • SAM-e · HelpedBut I did also begin taking SAM-e recently and I like it. It’s supposed to help with the mood/ happy neurotransmitters. In context ↗
  • vitamin C · Not saidPlus i take all the typical vitamin C In context ↗
  • mag. Glycinate · No changeI do take mag. Glycinate and Vit D3 with K2 and have long term. That did nothing for anxiety or depression. In context ↗
  • omega 3 · No changeThe omega 3 did nothing for me either In context ↗
  • generic Walmart brand of Allegra · HelpedThe take the generic Walmart brand of Allegra every day. That does help a lot with symptoms. In context ↗
  • Acyclovir · HelpedAlso Acyclovir is an anti viral that helps with LC as well. In context ↗
  • painful physical massage of neck and shoulder lumps · HelpedI have painful lumps in my neck and shoulders that I’m constantly trying to rub out( it helps a LOT to physically massage them out). And nut a gentle massage - a painful one. In context ↗
  • staring straight ahead instead of glancing around while driving · HelpedOnce I started just looking straight forward and not glancing around- it stopped. In context ↗

Approaches: Antibiotics · Antivirals · Stimulants · Supplements

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
February 2020long COVID began after an asymptomatic COVID infectionthe long covid hit me in Feb In context ↗Moderate
2020five weeks of severe chest pain, thought they were going to dieI thought I was going to DIE for 5 weeks in 2020. In context ↗Moderate
spring 2021five weeks of IV vitamin C and B for EBV; neuropathy gone and lost lymph fluidI lost 5 pounds of lymph fluid and my peripheral neuropathy was gone In context ↗ModerateIV vitamins and Myers cocktail
spring 2021all symptoms returned a month after the IV therapyBut it only lasted a month and it all came back. In context ↗Moderate
December 2023full taste and smell returned after a tick bite and Vive MineralsWithin less than a week AAALLL my taste and smell was back! In context ↗Moderate
summer 2024severe neurological issues and vertigo, could not drive for three monthsI had all kinds of really severe neurological issues in the summer of 2024 and I was unable to drive for about three months. In context ↗Moderate
August 2024POTS attack after two yellow jacket stings, laid down for a weekI had a horrible POTS episode, couldn’t stand , had massive air hunger In context ↗Moderate
August 2024restarted Adderall and all symptoms liftedALL my symptoms are GONE. I felt so great, no weakness, no exhaustion. In context ↗MildAmphetamine salts (Adderall)
April 2026still having flares of neuropathy, dry eyes and mouth, chest pain and air hunger six years inthe super dry eyes and dry throat / mouth occur In context ↗Moderate

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Neuropathy & tinglingI get a flare, and the peripheral neuropathy happens again In context ↗
  • Pain & fibromyalgiathe joint pain, muscle pain and sudden bursitis in my left hand In context ↗
  • Brain fogI have the depression, brain fog, OCD In context ↗
  • Anxiety & low moodSince long Covid ( Feb 2020) I struggle with depression. In context ↗
  • Sleep problemsI have severe insomnia from long Covid In context ↗
  • Heart symptoms & palpitationsEvery time I get Covid now, my chest pain flares. In context ↗
  • POTS & dysautonomiaI had a horrible POTS episode, couldn’t stand , had massive air hunger In context ↗
  • Mast cell (MCAS) & allergiesI have all the typical MCAS symptoms. In context ↗
  • BreathlessnessI would begin to get air hunger In context ↗
  • Hair lossthe anhedonia, bouts of anxiety, hair falling out In context ↗
  • Loss of smell or tasteafter 4 years of on and off ( never good/ normal) taste and smell, I have it ALL back- like 100% In context ↗
  • Gut problemsEvery system in my body, including my gut, is inflamed. In context ↗
  • Muscle weaknessmy back would go weak , I get tachycardia In context ↗
  • Vision problemsfeel like I have sand in my eyes because they’re so dry In context ↗

Ask Miruvor AI

Asking aboutFox 33206’s story

Similar stories

  • Mostly bedbound with ME/CFS and POTS, now housebound after tVNS and pacing

    Somewhat better Crane 62793 ME/CFS Severe at worstIll 3.5 years before improving or writing reddit.com Oct 2026

    Crane 62793, a UK adult in their mid-30s, developed ME/CFS after a COVID infection, with symptoms starting in 2022-2023: first mild then moderate-severe with PEM, brain fog and migraines. A crash in October 2025 left them mostly bed bound and they developed…

  • Mostly in bed with ME/CFS, partial gains from LDN and IV fluids then relapses

    Relapsed Trail 92725 ME/CFS Severe at worstIll 4 years before improving or writing reddit.com Oct 2026

    Trail 92725, in the UK, dated their decline to the first vaccines in early 2021 and was mostly in bed by 2025, on top of long-standing POTS, MCAS and hEDS. LDN, weekly IV fluids, aciclovir, ketotifen and mestinon brought partial gains, but crashes in October…

  • Long COVID, barely walking at worst, now much better with pacing and gluten-free diet

    Much better Trail 69409 Long COVID Moderate at worstIll 6 years before improving or writing reddit.com Oct 2026

    She caught COVID in May 2020 and had years of relapsing fatigue, brain fog, depression and insomnia, at worst barely able to manage stairs or walk in a straight line while still working from home. Vaccines gave gains that faded; pacing and a gluten-free diet…

  • Severe ME/CFS improved to mild, then relapsed after covid; still unable to work

    Relapsed Quail 79609 ME/CFS Ill 12 years before improving or writing reddit.com Oct 2026

    After norovirus and a hospitalised 'pneumonia' in late 2014 she developed ME/CFS and was severe. Antivirals, LDN, TUDCA and B12 injections lifted her to mild, but a June 2024 covid infection erased the gains and forced her off LDN. Nicotine patches later…

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