Miruvor
Sign up
Long COVID Moderate → relapsedIll 10 months before improving or writing

Long COVID with POTS and vertigo, brief improvement then relapse; lorazepam helped a bit

Condition
Long COVID
At worst
Moderate (mostly housebound)
Ill before improving or writing
10 months
Last post
Oct 2022
In their words
  • Condition: Long COVIDIm 2 weeks into the 9th month of long covid. In context ↗
  • At worst: ModerateI cant go out and exercise, i cant walk my dog. I cant cook and sitting in a chair doesnt help. In context ↗
  • Now: RelapsedI have had this 24 hours a day since february. Physiotherapy has helped a bit. In context ↗
  • Began after: COVIDI was able to eat during covid. In context ↗
Read from 14 of their posts and comments; links to the 10 this page draws on

Request to remove this story

Summary

A long COVID patient who fell ill around December 2021 had a brief improvement before their original symptoms returned in July 2022; by nine months they were still unwell, with POTS, and 24-hour vertigo dating from February 2022. They could not walk their dog, cook or exercise, and a short walk around the block left them dizzy enough to need a lift home. Lorazepam helped somewhat and physiotherapy helped a bit, but the dizziness persisted.

Ask Miruvor AI

Asking aboutMaple 85040’s story

What they tried

Also tried

meal replacement drinks like Boost or Ensure· Helpedlorazepam· Helpedstaying in bed· Helpedphysiotherapy· Helpedbeta blockers· Worsemarijuana edible· Not said
Their words about each treatment
  • meal replacement drinks like Boost or Ensure · HelpedI had to buy meal replacement drinks like Boost or Ensure to keep my calories up. In context ↗
  • lorazepam · HelpedBut i also take lorazepam 3 times a day which definitely helps with lowering it. In context ↗
  • beta blockers · WorseI dont respond well to beta blockers. In context ↗
  • marijuana edible · Not saidSo my dad gave me a marijuana edible thinking it would help. In context ↗
  • staying in bed · Helpedonly thing that kind of helps right now is lorazepam and staying in bed. In context ↗
  • physiotherapy · HelpedPhysiotherapy has helped a bit. In context ↗

Their path

Very severeSevereModerateMildNear normalRecovered6 mo9 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 6 months after onset: the story doesn’t say how ill they were before that. 2 steps say too little to place on the scale and are only in the table. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they were
around December 2021COVID-19 infection, followed by long COVIDI was able to eat during covid. In context ↗Not stated
February 202224/7 vertigo and dizziness beganI have had this 24 hours a day since february. In context ↗Not stated
June to early July 2022a good stretch; could walk around the block without trouble2 weeks ago I was able to walk around the block with no problem. My heart wasnt even pounding much if at all. In context ↗Mild
2022-07-23crashed on a walk around the block; original symptoms returnedI tried going for a walk around the block and my eyes couldn't focus on all the trees and sky and i got so dizzy i had to find a bench to sit down In context ↗Moderate
2022-10-02still ill with POTS and constant vertigo; physiotherapy gave a little helpI have had this 24 hours a day since february. Physiotherapy has helped a bit. In context ↗Moderate

Adverse events

Symptoms mentioned

Their words about their symptoms
  • POTS & dysautonomiaPots is absolutely irritating me. It controls everything i do. In context ↗
  • Heart symptoms & palpitationsHeart spikes for me when standing at certain times of the day. In context ↗
  • Vision problemsmy eyes couldn't focus on all the trees and sky In context ↗
  • Headaches & migraineIf i scrub my head i get dizzy through the eyes and head pressure. In context ↗
  • Anxiety & low moodI just feel like crying all day now In context ↗
  • Gut problemsChewing foods made me nauseous. In context ↗
  • Loss of smell or tasteI got my taste back 5 weeks after my first symptom. In context ↗

Ask Miruvor AI

Asking aboutMaple 85040’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