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Long COVID Mild → much betterIll 14 months before improving or writingNeeds ongoing treatment

Long COVID fatigue, brain fog and dizziness, much better after maraviroc and fluvoxamine

Condition
Long COVID
At worst
Mild (working or studying, with limits)
Ill before improving or writing
14 months
Last post
Sep 2026
In their words
  • Condition: Long COVIDGot the OG strain back in Jan 2021 and it’s been 2.5 years of hell. In context ↗
  • At worst: MildWorking outside home. Had no business doing that for a long time but I have a family to provide for so I just took it slow as possible. In context ↗
  • Now: Much betterNot fully recovered. I still have heart rate issues (Inappropriate Sinus Tachycardia) is the official diagnosis. Low energy depending on the day. But I’ve come a long way. In context ↗
  • Began after: COVIDGot the OG strain back in Jan 2021
  • Says they never had: Post-exertional malaiseNo PEM. Able to do zone 2 exercise.
Read from 134 of their posts and comments; links to the 46 this page draws on

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Summary

A 41-year-old New York man caught the original COVID strain in January 2021 and never recovered, working full-time through fatigue, a racing heart, tingling, brain fog and dizziness. Maraviroc, fluvoxamine and as-needed metoprolol helped; despite an earlier crash from the Levine exercise protocol, he was about 85% better by early 2023. A third infection set him back, and three-plus years on he still had tachycardia, tinnitus and low energy.

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What they tried

Their words about each treatment
  • Levine Protocol / steady-state cardio · Much worseI followed it exactly as it was for 3 months and then had my worst flare to date. In context ↗
  • Fluvoxamine · HelpedFluvoxamine - helped with vision issues within 2 days In context ↗
  • Crestor (statin) · Not saidStatin - I was already on Crestor due to familial hypercholesterolemia. In context ↗
  • Ivermectin · HelpedIt helped me some with fatigue. In context ↗
  • Prednisone · HelpedI’ve noticed when on anti inflammatories (prednisone or colchicine) my vision is better but as soon as I’m off them it goes back to baseline crappy. In context ↗
  • Maraviroc · Helped a lotThis was the game changer for me. In context ↗
  • B12 · HelpedB12 - 3000 mcg a day really helped with my energy. In context ↗
  • Fasting / intermittent fasting · Worseit was actually fasting that caused the HR elevation, not keto. In context ↗
  • Antihistamines (Zyrtec, Claritin) · No changeI tried Zyrtec, Claritin, famotidine and a low histamine diet. Didn’t help any unfortunately. In context ↗
  • Zinc · Not saidSecond infection I just took more vitamins (specifically zinc, Vitamin C) and hydrated and rested. In context ↗
  • Magnesium · No changeI took magnesium for about 90 days. I didn’t notice any positive effect. In context ↗
  • Probiotics · Not saidprobiotics, B1, Quercetin, etc. In context ↗
  • Low-dose aspirin · No changeno difference that I can physically tell In context ↗
  • Metoprolol (beta blocker) · HelpedA beta blocker (metoprolol) has been really helpful. In context ↗
  • Amoxicillin · Not saidI’ve taken Amoxicillin for strep and then another time for an ear infection with LC. I didn’t notice any changes. In context ↗
  • Time · HelpedReally just time In context ↗
  • Strict keto (4:1) · WorseI did strict Keto (4:1 ) for 6 weeks measuring with a ketone meter. Made my tachycardia way worse! In context ↗
  • Visibiome · No changeI tried Visibiome but it didn’t appear to help anything. In context ↗
  • Colchicine · HelpedI was prescribed Colchicine specifically for gout, but I noticed it helps with my long COVID blurry vision quite a bit. In context ↗
  • Extra table salt in water · No changeI took extra table salt mixed with water for about the first year to try and help with the HR issues. In context ↗
  • Moderna COVID vaccine series · No changeDidn’t appear to make it worse but didn’t make me any better either. In context ↗
  • Creatine · No changeDidn’t notice a difference when I took it. In context ↗
  • Taurine · No changeCurrently trying taurine for the vision stuff - but a week or so in no improvement. In context ↗
  • Paxlovid · Not saidI don’t know that any of it helped to be honest. In context ↗
  • Narrowband UVB · HelpedI’ve also done narrowband UVB which helped with heart rate and energy. In context ↗
  • NSAIDs · No changeCan’t say NSAIDs helped me unfortunately. In context ↗
  • THC · WorseIt was relaxing until my HR hit 140 and stayed there for like half an hour. In context ↗

Approaches: SSRIs · Antivirals · Supplements

Their path

Very severeSevereModerateMildNear normalRecoveredonset12 mo2 y3 y4 y5 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. 1 step has no time and sits in story order between the steps around it. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
January 2021COVID (OG strain); never got betterGot the OG strain back in Jan 2021 and it’s been 2.5 years of hell. In context ↗Mild
March 2022started Maraviroc after a bad flare; energy and heart rate began to improveI started it in March after a bad flare ... This was the game changer for me. In context ↗MildMaraviroc (Selzentry)
August 2022setback after strep throat and 10 days of amoxicillinGot strep throat and did 10 days of Amoxicillin the first of August. Feel crappy again In context ↗Mild
around 2 years inlowest point, but kept working full timemy worst was around 2 years in In context ↗Mild
February 2023second infection; energy rose afterwardsMost all my progress stayed but my energy got way higher. In context ↗Mild
March 2023about 85% recovered on twice-daily MaravirocI’d say 85% recovered. Can do mostly what I want but avoid alcohol and strenuous exercise. In context ↗MildMaraviroc (Selzentry)
December 2023third infection set back heart rate and energyI felt really good until my 3rd infection in December. Now just tired and the HR stuff isn’t great again. In context ↗Mild
—crashed after restarting exerciseI then started back exercising and about 6 weeks in had a crash. In context ↗Mild
September 2026far from onset but still limited by IST, tinnitus and low energy; first three good days in a rowI’m in my 6th year…FINALLY had 3 good days in a row. That’s never ever happened. Had my normal energy and felt 20 years younger. In context ↗Mild

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Brain fogI had brain fog, forgetfulness and problems with word recall for several years. It mostly resolved with time In context ↗
  • POTS & dysautonomiaI still have heart rate issues (Inappropriate Sinus Tachycardia) is the official diagnosis. In context ↗
  • Sleep problemsIt went from feeling tired after sleeping 9 hours and then wanting/taking a nap two hours later In context ↗
  • Headaches & migraineCurrent symptoms are tachycardia, tinnitus, headaches, low energy. In context ↗
  • Heart symptoms & palpitationsMy palpitations went away but I still get the hard beats 2.5+ years in. In context ↗
  • Neuropathy & tinglingI had numbness/tingling in my face, feet and hands. Mostly my left side. In context ↗
  • Anxiety & low moodProbably 18 months to totally get the anxiety back to normal. In context ↗
  • TinnitusI guess then one thing that hasn’t changed any is the tinnitus in my left ear. It is outta control! In context ↗
  • Temperature regulationout of nowhere my autonomic nervous system decides it’s gonna make my heart race, me sweat and not regulate body temp In context ↗
  • Vision problemsStill have eye issues too (mainly more blurry now as opposed to blurry and bothering me where I was rubbing my eyes a lot). In context ↗

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