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

Housebound with long COVID, now much better after SS-31 and meditation

Condition
Long COVID
At worst
Severe (mostly bedbound)
Ill before improving or writing
14 months
Last post
Aug 2025
In their words
  • Condition: Long COVIDI’ve had long covid since November of 2023. In context ↗
  • At worst: SevereAt my worst I literally could do nothing but lie on the floor and pant. In context ↗
  • Now: Much betterPersonally I have gone from severe to mild by addressing mitochondrial dysfunction and chronic inflammation. In context ↗
  • Began after: COVIDwoke up sick with covid the next day
  • Says they never had: Mast cell (MCAS) & allergiesI don’t have MCAS
Read from 100 of their posts and comments; links to the 41 this page draws on

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Summary

Lagoon 55763 developed long COVID in November 2023 after a COVID infection following a 40 km mountain hike, and in July 2024 was housebound, lying on the floor all day. From December 2024 they built a mitochondrial protocol centred on the peptide SS-31, supplements and daily meditation, going from severe to mild-moderate and able to lift weights and walk miles, though still limited, not fully recovered and still having bad days and PEM. SS-31 cost $150 a vial.

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What they tried

Their words about each treatment
  • essential oil smell training · Helped a lotWithin a few days I could just barely start to smell them, and this gave me the encouragement to keep doing it till everything went back to normal. ... In the end I recovered my sense of smell much more rapidly than anyone else I knew (about 9 days). In context ↗
  • cannabis (THC/CBD) · HelpedCannabis is amazing for rapid recovery from symptoms. In context ↗
  • shrooms (psychedelics) · WorseEver since I got LC shrooms make me feel TERRIBLE. In context ↗
  • NAC · No changeI have never noticed NAC do anything except make hangovers almost non-existent In context ↗
  • NADH (sublingual powder / ENADA lozenges) · Helpedsublingual NADH definitely helps me In context ↗
  • PQQ · HelpedI believe PQQ also helps, though less noticeably than sublingual NAD. In context ↗
  • NMN · HelpedSS-31, NMN, PQQ, ALCAR, D-Ribose, ubiquinol, egcg, curcuminoids + piperine, SAM-e/betaine, omega 3, LDN. In context ↗
  • Optinad · HelpedOptinad is oral and works very noticeably but it made me very irritable for some reason and it’s kind of expensive. In context ↗
  • LDN · Helpedanecdotally that LDN appears to be helping me with fatigue In context ↗
  • cold showers and ice packs · HelpedAlternating hot and cold showers make me feel better, as well as ice pack on the upper chest/back of neck. In context ↗
  • journaling · HelpedMeditation and journaling for psychological relief. In context ↗
  • meditation (Waking Up app) · HelpedThe catalyst for those psychological changes was meditation every single day using the Waking Up app. In context ↗
  • tropisetron · HelpedEvery time I’ve dosed it, I’ve noticed a modest yet rapid relief of inflammation and brain fog. In context ↗
  • bupropion · No changeBupropion doesn’t do much for dopamine, speaking personally and based on some evidence. In context ↗
  • NSAIDs · No changethe relief is far more pronounced than anything I’ve gotten from NSAIDs In context ↗
  • H1 antihistamines (fexofenadine) · No changeI went all the way and sourced experikenra tetramethoxyluteolin (possibly the most potent mast cell inhibitor in existence) and none of these did anything for me. In context ↗
  • fasting · Worseto be honest fasting just makes me feel worse In context ↗
  • oxaloacetate · Not saidI am also experimenting with oxaloacetate and apigenin. In context ↗
  • SS-31 · Helped a lotFor almost the entire 100 days I did 2 mg per day. It really helped a lot and I’ve gained ground In context ↗
  • D-ribose · HelpedI’m actually new to D ribose but definitely feel a difference. In context ↗
  • creatine · Helpedcreatine 5 g per day - facilitates ATP production In context ↗
  • ALCAR · HelpedI’ve always found taurine, pqq and alcar helpful and I continue to take them. In context ↗
  • EGCG · HelpedI believe they did help because they’ve been demonstrated in research to directly inhibit IDO/TDO In context ↗
  • curcumin (curcuminoids) with piperine · HelpedI also take curcumin extract w/ piperine, egcg and trans-resveratrol to attenuate the IDO/TDO pathway In context ↗
  • trans-resveratrol · Helpedegcg, curcuminoids, trans-resveratrol <- these 3 directly downregulate the inflammatory IDO/TDO chronix upregulation seen in post-viral fatigue but they must be taken with piperine for absorption. In context ↗
  • taurine · HelpedTaurine has a slight calming effect and helps balance the jitteriness of caffeine. In context ↗
  • pacing (hard limits on activity) · HelpedBehavioral changes - Setting hard limits on my activities. In context ↗
  • modafinil · HelpedI really like 100 mg and only use 200 on days when I need to lock in and hyperfocus. In context ↗
  • methylene blue · No changeI personally was never impressed with it on its own In context ↗
  • ProdromeGlia plasmalogens · HelpedI think it helped a little.. maybe? It’s just way, way too expensive for the marginal benefit. In context ↗
  • L-ergothioneine · HelpedNowadays I’m using L-ergothioneine, carnosic acid, lithium ascorbate, and intranasal skq1. ... feels cleaner and more effective than using polyphenols In context ↗
  • molecular hydrogen water · HelpedIt helps me avoid getting cooked by PEM In context ↗
  • l-arginine, citrulline and vitamin C · No changeCitrulline, l-arginine and vitamin c are useful supplements, but they did not help me recover In context ↗
  • hydration and sodium · HelpedLots of hydration and sodium help. In context ↗
  • therapy · Helpedpurposefully destressing through disciplined meditation practice and therapy In context ↗
  • Intermittent fasting · WorseYeah to be honest fasting just makes me feel worse. In context ↗

Approaches: CBT & mindset · Amino acids and carnitine · Mind-body practices · Pacing · Peptides · Supplements

Their path

Very severeSevereModerateMildNear normalRecoveredonset6 mo12 mo18 mo

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
November 2023long covid began after a 40 km mountain hike and a covid infectionIt started after I did a 40 kilometer hike up one of the tallest mountains in Ukraine and woke up sick with covid the next day. In context ↗Mild
June 2024briefly felt recovered, no symptoms on a long road tripBy June I thought I was basically cured. In context ↗Near normal
July 2024crash to a lower baseline, likely reinfection; lying on the floor all dayin July my LC came back with an absolute vengeance ... I would wake up, lie down on the meditation mat on my floor and stay there until night. In context ↗Severe
November 2024started getting somewhat functional againIt wasn’t until November I started getting somewhat functional again, though I still had fatigue, severe brain burning and emotional disturbances every day. In context ↗Moderate
January 2025mitochondrial protocol began to show resultsI basically just plateau’d until early January when my protocol (which I started in December) started to show results. In context ↗ModerateSS-31 (elamipretide)
February 2025got through a 5-hour political demonstration without crashingToday I was at a 5 hour physically intensive political demonstration for Ukraine and have not crashed (though I am quite tired). In context ↗ModerateSS-31 (elamipretide)
March 2025lifting weights and taking multi-mile walks 2-3 times a weekI went from not even being able to walk down the street without my heart pounding and my brain burning, to lifting weights and taking multi-mile walks 2-3 times a week. In context ↗MildSS-31 (elamipretide)
April 2025a bit of a relapseI too have had a bit of a relapse recently and while it’s demoralizing, it also means your progress was real. In context ↗Mild
August 2025still mild, not fully recovered, milder PEMI have gone from severe to mild by addressing mitochondrial dysfunction and chronic inflammation. In context ↗Mild

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseEven on my good days I get a little PEM and brain burning In context ↗
  • Brain fogFatigue, brain fog, brain burning from severe down to mild-moderate In context ↗
  • Headaches & migraineThese include brain fog, fatigue, headaches abd pressure, inflammation and pain in the sinus and intracranial tissues. In context ↗
  • Heart symptoms & palpitationsnot even being able to walk down the street without my heart pounding and my brain burning In context ↗
  • Anxiety & low moodI just start to contemplate suicide. In context ↗
  • Temperature regulationheat most definitely worsens my symptoms In context ↗
  • Loss of smell or tasteanosmia was practically my only symptom In context ↗

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