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Long COVID Near normalIll 20 months before improving or writing

Tingling, burning, numbness with long COVID, nearly back to normal on sleep and magnesium

Condition
Long COVID
At worst
Not stated
Ill before improving or writing
20 months
Last post
May 2026
In their words
  • Condition: Long COVIDstarted the week after I tested positive (September 1st, 2024) In context ↗
  • Now: Near normalLike 90-95% I would say. ... it doesn’t impact my daily life at all. In context ↗
  • Began after: COVIDThis was a very alarming symptom that started the week after I tested positive (September 1st, 2024)
Read from 3 of their posts and comments; links to the 2 this page draws on

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Summary

Petrel 46561 developed intense tingling, burning and numbness the week after a COVID-19 infection in September 2024, landing them in the ER. They credited sleep regulation, meditation, magnesium glycinate, alpha-lipoic acid, curcumin and electrolytes as it slowly eased over about nine months. By May 2026 they rated themselves 90-95%, with occasional tingling and a numb patch on one foot; a January 2026 reinfection caused a brief, milder flare.

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What they tried

Also tried

drinking enough water· Helped
Their words about each treatment
  • regulating my sleep · HelpedThings that helped me were regulating my sleep In context ↗
  • meditation · HelpedThings that helped me were ... meditation In context ↗
  • drinking enough water · HelpedThings that helped me were ... making sure I was drinking enough water In context ↗
  • magnesium glycinate · Helpedmagnesium glycinate ... occasional twitching that is managed well by the magnesium
  • alpha-lipoic acid · HelpedThings that helped me were ... alpha-lipoic acid In context ↗
  • curcumin (turmeric) · HelpedThings that helped me were ... curcumin (turmeric) In context ↗
  • daily electrolytes · HelpedThings that helped me were ... daily electrolytes In context ↗

Approaches: POTS medication · Mind-body practices · Radical rest · Supplements

Their path

Very severeSevereModerateMildNear normalRecovered12 mo15 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. The chart starts 10 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 were
September 2024COVID-19 infection, then intense neuropathy the following week that landed them in the ERThis was a very alarming symptom that started the week after I tested positive (September 1st, 2024) and landed me in the ER. In context ↗Not stated
2025-06-24neuropathy almost recovered after slow improvement over 9 monthsNeuropathy (tingling, burning, numbness) finally almost recovered after 9 months ... I’m back to living my normal life for the most part. In context ↗Near normal
January 2026flare after COVID reinfectionI tested positive again in January of this year and I had a bit of a flare (still much less severe) for a few days but recovered just fine In context ↗Mild
2026-05-10rated 90-95%, barely noticeable, does not impact daily lifeLike 90-95% I would say. I think it’s gotten as good as it’s going to get, but it’s better to the point that I can go a few days without thinking about it and it doesn’t impact my daily life at all. In context ↗Near normal

Symptoms mentioned

Their words about their symptoms
  • Neuropathy & tinglingWhat remains is occasional tingling, usually if I’m tired or I’ve overdone it, occasional wispy feelings on my legs, and a patch of numbness on the bottom of my left foot. In context ↗

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