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Long COVID Severe → no benefitIll for 1 year

Bedbound on many days with long COVID and dysautonomia, no improvement a year on

Condition
Long COVID
At worst
Severe (mostly bedbound)
Ill for
1 year
Last post
Jul 2026
In their words
  • Condition: Long COVIDIf anyone has dealt with pots/dysautomia from covid please tell me anything that has helped you. In context ↗
  • At worst: Severe25f, bed bound alot of days. In context ↗
  • Now: No benefitThis has caused me such depression and I miss my old life, I need it back or at least to feel like i can go for a walk without dying. In context ↗
  • Began after: COVIDpots/dysautomia from covid
Read from 1 of their posts and comments; links to the one this page draws on

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Summary

A 25-year-old woman has been ill for about a year with POTS and dysautonomia that followed COVID-19; she is bed bound on many days and misses her old life. Medications are not an option for her because of a severe adverse reaction. The illness has brought depression, and her goal is to walk again without feeling she is dying.

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Their path

Very severeSevereModerateMildNear normalRecovered12 mo12 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 12 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
about a year before 2026-07-26POTS/dysautonomia after COVID-19If anyone has dealt with pots/dysautomia from covid In context ↗Not stated
2026-07-26bed bound on many days, no treatment yet25f, bed bound alot of days. In context ↗Severe
2026-07-26still struggling, asking for POTS tipsim struggling. 25f, bed bound alot of days. In context ↗Severe

Symptoms mentioned

Their words about their symptoms

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