Miruvor
Sign up
Long COVID Mild → near normalIll 20 months before improving or writing

Long COVID with tachycardia and joint pain, now nearly back to normal

Condition
Long COVID
At worst
Mild (working or studying, with limits)
Ill before improving or writing
20 months
Last post
Jan 2023
In their words
  • Condition: Long COVIDSince my Covid infection in May 2020, I have been experiencing joint pain/swelling. In context ↗
  • At worst: MildI have to work but I have to sleep. In context ↗
  • Now: Near normalNow 2.5 yrs later, most everything is back to normal except my joints. In context ↗
  • Began after: COVIDSince my Covid infection in May 2020
Read from 9 of their posts and comments; links to the 9 this page draws on

Request to remove this story

Summary

A nurse who caught COVID in May 2020 at age 49 was ill for three weeks, then kept tachycardia, joint swelling and pain, poor sleep and word-finding trouble. They improved gradually, and by January 2023, about 2.5 years in, most of it was back to normal except their joints. They took Wellbutrin for post-COVID anxiety and depression and NSAIDs daily for joint pain; a December 2020 vaccine changed nothing.

Ask Miruvor AI

Asking aboutGlade 52687’s story

What they tried

Their words about each treatment
  • Wellbutrin · HelpedWellbutrin helped with my anxiety/depression from this journey In context ↗
  • NSAIDs · HelpedI am taking NSAIDS every day & they help some In context ↗
  • glucosamine/chondroitin · No changeI also started glucosamine/chondroitin a couple of months ago but have not experienced any relief In context ↗
  • Benadryl · WorseI tried Benadryl but I feel so loopy in the morning after In context ↗
  • gabapentin · WorseMy doctor gave me gabapentin. Oh man. Nope. In context ↗
  • Flexeril · WorseFlexeril. Knocked me out for 10 hrs. In context ↗
  • statin · Helped a lotThe only thing that got my levels in order was a statin In context ↗
  • edibles · WorseI tried to use edibles for insomnia & it gave me panic attacks. In context ↗
  • vegetarian diet · No changeI went vegetarian at one point & it made no difference to my Cholesterol In context ↗
  • COVID vaccine · No changeVaccine in Dec 2020 resulted in no change to symptoms In context ↗

Their path

Very severeSevereModerateMildNear normalRecoveredonset12 mo2 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 were
May 2020COVID-19 infection, ill for three weeksI was hit pretty hard & was ill for 3 wks. In context ↗Mild
January 2022mostly back to normal, hands and word-finding still affected20 months after my infection & Im mostly back to normal. In context ↗Near normal
2022-01-15joint pain and swelling progressively worseningIt is progressively worsening, especially in my hands/shoulders/ankles. In context ↗Mild
2022-03-04slight improvement, brain fog and joint issues remainI can’t tell if I’ve just gotten used to it or if things have improved a little. Still struggle with the brain fog & joint issues but I’m rolling with it. In context ↗Mild
2023-01-07most everything back to normal except jointsNow 2.5 yrs later, most everything is back to normal except my joints. In context ↗Near normal

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Pain & fibromyalgiaThe joints in my hands, wrists, knees, ankles & feet still swell/hurt off & on. In context ↗
  • Brain fogI still struggle with spelling & finding the words I want to use when conversing. In context ↗
  • Sleep problemsI can’t get comfortable ... stay there longer than 5-6 hrs In context ↗
  • Heart symptoms & palpitationsThe tachycardia never went away after In context ↗
  • Anxiety & low moodI also had never had a panic attack in my life until after Covid & now I’m on Wellbutrin for anxiety/depression. In context ↗

Ask Miruvor AI

Asking aboutGlade 52687’s story

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