Miruvor
Sign up
Long COVID Somewhat betterNeeds ongoing treatment

Long COVID with fatigue, POTS and PEM, somewhat better on tirzepatide

Condition
Long COVID
At worst
Not stated
Ill before improving or writing
Not stated
Last post
Sep 2026
In their words
  • Condition: Long COVIDI got long covid before the vaccine was available. In context ↗
  • Now: Somewhat betterIt has been life changing. I still can get PEM and have to pace, but I have been able to do more In context ↗
  • Began after: COVIDI got long covid before the vaccine was available. In context ↗
Read from 10 of their posts and comments; links to the 7 this page draws on

Request to remove this story

Summary

Osprey 67987 got long COVID before vaccines were available, with fatigue, hyperadrenergic POTS, mast cell problems, temperature dysregulation and PEM requiring pacing. A first mRNA vaccine seemed to help, the bivalent one made things worse and Novavax was tolerated fine. Tirzepatide, split-dosed at a lower dose, was called life changing, with better energy and less fatigue, though PEM and the need to pace persisted.

Ask Miruvor AI

Asking aboutOsprey 67987’s story

What they tried

Their words about each treatment
  • trizepitide · Helped a lotTrizepitide has brought me actual rest and energy. It has been life changing. In context ↗
  • guanfacine · HelpedI has helped with my hyperpots and ADHD. In context ↗
  • Mast Cell stabilization · HelpedGuanfacine and Mast Cell stabilization In context ↗
  • magnisium · No changenothing prunes, hydration and magnisium didn't help for me In context ↗
  • pace · Not saidI still can get PEM and have to pace In context ↗
  • COVID vaccines (first mRNA, bivalent, novavax) · Not saidFirst mRNA seemed to help. The bivalent seemed to make things worse. I tolerate novavax fine. In context ↗

Approaches: GLP-1 drugs

Their path

Very severeSevereModerateMildNear normalRecovered

How ill they were on the ME/CFS severity scale, estimated from what they describe at each point, in the order they describe; they don’t give enough times to place each step. Hover or tap a point. 3 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 wereAfter
2020long COVID onset before vaccines were availableI got long covid before the vaccine was available. In context ↗Not stated
—first mRNA vaccine seemed to helpFirst mRNA seemed to help. In context ↗Not stated
—bivalent vaccine made things worseThe bivalent seemed to make things worse. In context ↗Not stated
2026tirzepatide brought rest, energy and less fatigueTrizepitide has brought me actual rest and energy. It has been life changing. In context ↗MildTirzepatide (Mounjaro, Zepbound)
August 2026can do more before PEM but still has to paceIt has increased my energy recovery and while I still have to pace, I can do more before signs of PEM. In context ↗MildTirzepatide (Mounjaro, Zepbound)

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI still can get PEM and have to pace In context ↗
  • POTS & dysautonomiaI have hyper POTS. In context ↗
  • Mast cell (MCAS) & allergieshelp with mast cell stabilization In context ↗
  • Temperature regulationI have had luck helping temp regulation with guanfacine. In context ↗

Ask Miruvor AI

Asking aboutOsprey 67987’s story

Similar stories

  • Housebound and mostly in bed with ME/CFS, now much better on rapamycin and low-carb diet

    Much better Flint 23355 ME/CFS Severe at worstIll 10 years before improving or writing reddit.com Oct 2026

    Ill for over a decade, Flint 23355 was at worst housebound and mostly in bed. Over the years she improved, crediting a low-carb, high-fat diet, iron infusions and rapamycin at 4 mg, which helped PEM after a direct 6 mg start caused a massive crash; weekly…

  • Severe, housebound ME/CFS, somewhat better with pacing and low-dose naltrexone

    Somewhat better Harbor 19162 ME/CFS Severe at worstIll 8 years before improving or writing reddit.com Oct 2026

    A UK woman ill with ME/CFS for eight years, severe and housebound since 2021 after graded walks left her wheelchair dependent. She credited pacing and low-dose naltrexone with steady gains, and later a low-histamine diet with curing insomnia, migraines,…

  • Long COVID at its worst mostly lying down, now nearly back to normal with Zepbound

    Near normal Alpine 44425 Long COVID Severe at worstIll 2 years before improving or writing reddit.com Oct 2026

    Ill with long COVID from July 2024; at worst sleeping or lying down most of the day, barely functioning, with fatigue, PEM, brain fog, palpitations and POTS. Antihistamines and supplements raised energy within a week, and nattokinase, bromelain and curcumin…

  • Long COVID made work impossible, now somewhat better with pacing and GLP-1 drugs

    Somewhat better Puffin 16593 Long COVID Severe at worstIll 4.5 years before improving or writing reddit.com Oct 2026

    He caught COVID in 2022 during Omicron when his son started daycare and kept getting sicker as daycare infections piled up; symptoms peaked about a year in and work became impossible. He improved after a long COVID clinic helped with management and he…

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