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Long COVID Mild → somewhat betterIll 2 years before improving or writingNeeds ongoing treatment

Long COVID with POTS and brain fog, somewhat better; hydration and rowing eased POTS

Condition
Long COVID
At worst
Mild (working or studying, with limits)
Ill before improving or writing
2 years
Last post
Apr 2022
In their words
  • Condition: Long COVIDDoes This Sound Like Long Covid? 2 Years of Evolving Symptoms In context ↗
  • At worst: MildI am a previously healthy young adult male starting my college years but have developed debilitating symptoms over time. In context ↗
  • Now: Somewhat betterThe Dysautonomia seems to have gotten better over time, though. In context ↗
  • Began after: COVIDI was sick in March 2020 before the lockdown but it felt like a cold so I brushed it off as unimportant In context ↗
Read from 2 of their posts and comments; links to the 2 this page draws on

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Summary

Plover 39492, a young male college student, fell ill in March 2020 with a cold-like illness and over two years developed vision loss from a branch retinal artery occlusion, Raynaud's, POTS with palpitations and chest pain, then brain fog, headaches and dizziness. Hydration and rowing eased the POTS by April 2022, but blood pooling in heat and dense brain fog remained.

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What they tried

Their words about each treatment
  • drinking loads of water · HelpedHowever in the evening, if I properly hydrate, I'm able to get out of POTS range where my hr jumps to just 75 bpm when standing. In context ↗
  • rowing at the gym · Helpedafter drinking loads of water and rowing at the gym, my resting hr sits at about 55 bpm laying down In context ↗

Their path

Very severeSevereModerateMildNear normalRecoveredonset6 mo12 mo18 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
March 2020cold-like illness before lockdownI was sick in March 2020 before the lockdown but it felt like a cold so I brushed it off as unimportant In context ↗Mild
June 2020branch retinal artery occlusion; lost part of vision in right eyea portion of my vision in my right eye was completely gone In context ↗Mild
February 2021Raynaud's: fingers pale and numb in coldmy fingers went pale and numb In context ↗Mild
December 2021POTS onset: breathless with racing heart on standingGetting up after a brief late-night gaming sesh left me completely breathless and made my heart race super fast In context ↗Mild
April 2022dense brain fog, headaches and dizziness while in collegethat has developed into a dense fog that has clouded my mind ever since In context ↗Mild
2022-04-25dysautonomia eased with hydration and rowing at the gymThe Dysautonomia seems to have gotten better over time, though In context ↗Mild

Symptoms mentioned

Their words about their symptoms
  • Vision problemsa portion of my vision in my right eye was completely gone In context ↗
  • Temperature regulationThis has been happening in colder weather ever since In context ↗
  • POTS & dysautonomiaI still experience blood pooling in the heat and dread the upcoming summer In context ↗
  • Heart symptoms & palpitationsit jumps to and sustains at 90 bpm after standing up in the morning In context ↗
  • Breathlessnessleft me completely breathless In context ↗
  • Brain fogdeveloped into a dense fog that has clouded my mind ever since In context ↗
  • Headaches & migraineHeadaches are usually around my temples and eyes In context ↗

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