Miruvor
Sign up
Long COVID Moderate → somewhat betterNeeds ongoing treatment

Long COVID sinus tachycardia and brain pressure, somewhat better on ivabradine and PT

Condition
Long COVID
At worst
Moderate (mostly housebound)
Ill before improving or writing
Not stated
Last post
Oct 2026
In their words
  • Condition: Long COVIDI was throttled with COVID August 2023. I was sick for 18 days and confirmed with Inappropriate Sinus Tachycardia (IST) four months later. It has been a living hell ever since and I barely remember 2024. In context ↗
  • At worst: ModerateIt has been a living hell ever since and I barely remember 2024. ... I am able to move around now without feeling dizzy. I still cannot go on big inclines.
  • Now: Somewhat betterI had one day this week where I felt normal for the first time in 2.5yrs ... It has given me a little bit of life back.
  • Began after: COVIDI was throttled with COVID August 2023.
Read from 47 of their posts and comments; links to the 25 this page draws on

Request to remove this story

Summary

After COVID in August 2023 (18 days ill, two hospital visits) they developed inappropriate sinus tachycardia and raised intracranial pressure and barely remember 2024. Ivabradine from December 2023 and autonomic physical therapy cut their tachycardic burden and eased their dizziness. Microdosed tirzepatide and metformin brought days that felt normal and 10k steps in 2026, though big inclines still limit them.

Ask Miruvor AI

Asking aboutBeacon 71899’s story

What they tried

Their words about each treatment
  • propranolol · WorseI had rare side effects with propranolol ... the propranolol affected my TSH, T3 AND T4 In context ↗
  • diltiazem · Worsepropranolol was terrible for me and I was on diltiazem for 48 hrs. I swelled up like crazy In context ↗
  • Corlanor (ivabradine) · Helped a lotI have IST from COVID and Ivabradine has helped. I am slowly decreasing my dose In context ↗
  • Magnesium glycinate or magnesium taurate · HelpedMagnesium glycinate or magnesium taurate are game changers for tachycardia In context ↗
  • CoQ10 · HelpedThe CoQ10 helps the magnesium absorb better In context ↗
  • melatonin · Helpedthe melatonin gets rid of my primary stabbing headache (thanks COVID) In context ↗
  • MyCommunity Comprehensive Mushroom Blend · HelpedI find that taking MyCommunity Comprehensive Mushroom Blend is helpful to boost immunity In context ↗
  • Slynd (progesterone only pill) · WorseSlynd is derived from a loop diuretic and dumps sodium. I learned that the hard way! In context ↗
  • Cipro · Much worseCipro messed me up for years. Check into a sensitivity test. In context ↗
  • compression socks · WorseI also had issues with compression socks. Wearing them significantly increased my resting heart rate In context ↗
  • parasympathetic and vestibular physical therapy · Helped a lotI have been going to parasympathetic PT for 11 months. It has helped to reduce my tachycardic burden from 70%, to 46% and now 13% In context ↗
  • metformin · HelpedI feel like the metformin helps with brain fog In context ↗
  • tirzepatide · HelpedThe lil bae dose .25mg helped me go on a hike last week without any issues. I also had actually energy to do things. In context ↗
  • meditation · HelpedMeditation is also very powerful in my experience. In context ↗

Approaches: GLP-1 drugs · POTS medication · Other drugs and medicines

Their path

Very severeSevereModerateMildNear normalRecovered12 mo18 mo2 y2.5 y3 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. The chart starts 10 months after onset: the story doesn’t say how ill they were before that. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
2024Inappropriate sinus tachycardia and raised intracranial pressure; barely remembers the yearIt has been a living hell ever since and I barely remember 2024. Prior to COVID, I was active and hiking at high altitude. In context ↗Moderate
February 2025Started physical therapy focused on calming the autonomic systemI started going to PT for a shoulder injury and mentioned to my PT that I have autonomic dysfunction. In context ↗Moderate
September 2025Eight months of parasympathetic and vestibular PT reduced tachycardia; no longer dizzy moving aroundI feel like my IST symptoms are getting better with parasympathetic and vestibular physical therapy. In context ↗Mild
late 2025Setback after starting a progesterone-only contraceptiveI had a great Summer with a huge drop then has a setback taking a progesterone only contraception that I gave since stopped. In context ↗Mild
January 2026Hiked stairs and walked 10k steps on microdosed tirzepatide plus metforminI went on a hike with multiple stairs for the first time since this Summer. ... I also walked 10k steps two days before In context ↗MildTirzepatide (Mounjaro, Zepbound)
14 January 20260.5 mg tirzepatide drove IST into high gear with blood pressure and blood sugar problemsThis .5mg dose drove my IST into high gear, caused blood pressure and blood sugar issues. In context ↗Mild
October 2026Low-dose metformin and tirzepatide; brain fog better, days that feel normalI take metformin and glp-1. I low dose both. 250mg split 2x/day. It helps with brain fog. I also split dose tirzepatide 1.45 split 2x/week. In context ↗MildTirzepatide (Mounjaro, Zepbound)

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Heart symptoms & palpitationsI have Inappropriate Sinus Tachycardia (IST) thanks to COVID. My RHR while sleeping was 105 before I was medicated. In context ↗
  • Brain fogI feel like the metformin helps with brain fog In context ↗
  • Headaches & migraineI am seeing a Neurologist next Friday for the fun migraines! In context ↗
  • TinnitusI don't have the whooshing sound in my ear anymore or wake up with headaches if I am not elevated at night. In context ↗

Ask Miruvor AI

Asking aboutBeacon 71899’s story

Similar stories

  • Bedbound with ME/CFS after COVID, some improvement with low-dose naltrexone and ivabradine

    Somewhat better Crocus 16327 ME/CFS Severe at worstIll 15 years before improving or writing reddit.com Oct 2026

    She had 15 years of gradual ME/CFS symptoms with teenage EBV and crashes during her PhD, then became bedbound after COVID in early 2024. Diagnosed with ME/CFS, POTS, MCAS and hEDS in 2025, she credits low-dose naltrexone, ivabradine, H1/H2 antihistamines and…

  • Bedbound with long COVID, now much better with pacing and low-dose naltrexone

    Much better Cedar 29323 Long COVID Severe at worstIll 10 months before improving or writing reddit.com Sep 2026

    Cedar 29323 caught COVID in December 2021 and developed long COVID on top of lupus and ADHD. She worked until a crash at six months left her bedbound, then stopped working in August 2022 and slowly improved. Low-dose naltrexone, stellate ganglion blocks,…

  • Not enough detail to draw a path

    ME/CFS worsened to moderate after Pfizer; still moderate, amitriptyline helped sleep

    Somewhat better Island 75834 ME/CFS Moderate at worstIll 18 years before improving or writing reddit.com Sep 2026

    Island 75834 had mild ME/CFS, working part-time and doing a PhD, until after a June 2021 Pfizer vaccination they worsened from mild to moderate and had to quit their part-time job. They also had worsened POTS and brain fog; amitriptyline helped their…

  • Nearly bedbound with long COVID, now close to normal after ganglion blocks and nicotine

    Near normal Dusk 66875 Long COVID Severe at worstIll 3.5 years before improving or writing reddit.com Oct 2026

    A former daily 5K runner, he caught COVID and was nearly bedbound in the second month with dysautonomia and PEM. Over more than two years he tried many treatments, crediting stellate ganglion blocks and nicotine, and was trying rapamycin. He was not fully…

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