Long COVID
Severe → no benefitIll for 2 years
Long COVID, unable to work physically or mentally, with no improvement reported
- Condition
- Long COVID
- At worst
- Severe (mostly bedbound)
- Ill for
- 2 years
- Last post
- Apr 2024
In their words
- Condition: Long COVID
after I had Covid and 2 years of being sick
In context ↗ - At worst: Severe
I have no life and I feel like I’m just the bed rotting corpse.
In context ↗ - Now: No benefit
I pushed for almost a year slowly just getting worse at my job
In context ↗ - Began after: COVID
a year after I had Covid
Read from 1 of their posts and comments; links to the one this page draws on
Summary
A veterinary professional who became ill with COVID-19 pushed through work for almost a year, steadily worsening until they could not assist in surgery. Two years into the illness they were on disability after an MCAS diagnosis, unable to work physically or mentally, and described having no life and feeling like a 'bed rotting corpse'. They said vaccine doses worsened their immune system. No treatments or improvement were reported.
Ask Miruvor AI
What they tried
Also tried
Their words about each treatment
- COVID vaccination as treatment · Worse
the vaccines kicked my ass and immune system
In context ↗
Their path
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
| When | What happened | Where they were |
|---|---|---|
| 2022 | became ill after COVID, kept working in vet med2 years of being sickIn context ↗ | Mild |
| 2023 | pushed through work and slowly got worseI pushed for almost a year slowly just getting worse at my jobIn context ↗ | Mild |
| 2024-04-07 | on disability after MCAS diagnosis, mostly in bedI have no life and I feel like I’m just the bed rotting corpse.In context ↗ | Severe |
Adverse events
- COVID vaccination as treatment“the vaccines kicked my ass and immune system” In context ↗ Made symptoms worse
Symptoms mentioned
Their words about their symptoms
- Mast cell (MCAS) & allergies
after my MCAS dx
In context ↗ - Brain fog
I physically and mentally can’t
In context ↗