Miruvor
Sign up
Long COVID Severe → somewhat betterIll 3 years before improving or writingNeeds ongoing treatment

Bedbound at times with long COVID chest pressure and tachycardia, somewhat better

Condition
Long COVID
At worst
Severe (mostly bedbound)
Ill before improving or writing
3 years
Last post
Jan 2026
In their words
  • At worst: SevereI’m basically bedbound as well In context ↗
  • Now: Somewhat betterThe pressure has lessened enough that I can function more, but not so much that I feel functional In context ↗
  • Began after: COVIDI got sick in March 2023 with my first and only known Covid infection.
Read from 50 of their posts and comments; links to the 23 this page draws on

Request to remove this story

Summary

COVID in March 2023 at 22 left them with constant chest pressure, worse on standing or walking, with tachycardia and breathlessness. They became housebound and at times bedbound; beta blockers, calcium channel blockers, ivabradine, nitrates and ranolazine gave little or no significant relief, and EECP worsened the pain. A January 2025 angiogram found coronary microvascular dysfunction and a myocardial bridge; open heart surgery was planned.

Ask Miruvor AI

Asking aboutPebble 68032’s story

What they tried

Their words about each treatment
  • Advair · No changeall the meds I’ve tried haven’t worked (Advair, albuterol, omeprazole, prednisone, NSAIDs, and probably more that I’m forgetting) In context ↗
  • resting · No changeI’ve been resting for almost 2 months straight with no improvement. In context ↗
  • magnesium · HelpedI take magnesium daily, I had some numbness and tingling on my left side in month 2-3 of LC and magnesium helped resolve that. In context ↗
  • pain meds · HelpedI’ve been on pain meds that significantly reduced the chest pain for a few weeks, but it’s nearly back at full force now even with the max amount of pain meds I can take. In context ↗
  • baby aspirin · WorseI’ve been taking baby aspirin since. Haven’t had an issue necessarily, but I do suspect it might be exacerbating my symptoms (chest pain/pressure, shortness of breath). In context ↗
  • iron supplements (Nature Made) · No changeThe iron supplements I took did boost my ferritin, but the iron supplements didn’t help my long Covid symptoms so I’m not taking them anymore. In context ↗
  • metoprolol · WorseI’ve been on metoprolol and diltiazem separately and neither have lowered my heart rate (120 resting) ... metoprolol gave me wicked migraines so I stopped it
  • diltiazem · HelpedI’ve been on a calcium channel blocker that has been somewhat helpful, but the chest pain is still basically constant. In context ↗
  • ivabradine · HelpedIt did lower my heart rate, which has slightly decreased the amount of chest pain I’m in In context ↗
  • nebivolol · HelpedI’ve been taking nebivolol for a little over a month and it’s made movement more tolerable, but still painful. In context ↗
  • SSRIs · No changebeta blockers, SSRIs, and ivabradine all have no impact on my chest pain In context ↗
  • meloxicam · WorseI took it for several months and it caused horrible mouth ulcers that took weeks to heal and significantly damaged my oral health. It also didn’t reduce my pain at all. In context ↗
  • nitrates (short acting and long acting) · No changeivabradine, and nitrates (short acting and long acting), all at varying doses and combinations- nothing has helped so far In context ↗
  • ranolazine · No changenitrates, ivabradine, and ranolazine. None have helped in any significant way. In context ↗
  • EECP (Enhanced External Counterpulsation) · Much worseI could only make it through a few sessions because it made my chest pain significantly worse. In context ↗

Their path

Very severeSevereModerateMildNear normalRecoveredonset12 mo2 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. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they wereAfter
March 2023COVID infection, constant chest pain from the startI started getting chest pain within 24 hours of testing positive In context ↗Moderate
September 2023symptoms worse at the 6 month markI just hit 6 months myself and would agree that my symptoms are worse. In context ↗Moderate
December 2023basically bedboundI’m basically bedbound as well… In context ↗Severe
March 2024heart rate and chest pain slightly reducedIt did lower my heart rate, which has slightly decreased the amount of chest pain I’m in In context ↗ModerateIvabradine
July 2024movement more tolerable on nebivololI’ve been taking nebivolol for a little over a month and it’s made movement more tolerable, but still painful. In context ↗Moderate
July 2025flare after wisdom teeth surgeryI had my wisdom teeth out 1.5 weeks ago under IV anesthesia and I’m still in a flare up. In context ↗Moderate
January 2026still housebound, awaiting heart surgeryI’m still more or less housebound. In context ↗Moderate

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Heart symptoms & palpitationsI also developed tachycardia and shortness of breath with my heart rate reaching 120bpm at rest In context ↗
  • BreathlessnessI get shortness of breath when I have to “exert” myself In context ↗
  • Neuropathy & tinglingI developed numbness/tingling on my left side as well, although that resolved with magnesium supplements. In context ↗
  • Post-exertional malaiseeven walking around a grocery store or picking up my meds from the pharmacy can cause a whole lot of pain for hours/days afterwards In context ↗
  • Brain fogmy brain fog is so bad it’s hard to work In context ↗
  • Gut problemsI do technically have IBS too but that’s been well controlled for years before I got Covid. In context ↗
  • Anxiety & low moodI have CPTSD from before LC and I actually felt like I was healing for a couple months before getting sick. In context ↗
  • POTS & dysautonomiaI think I have some orthostatic intolerance but the tachycardia was bad no matter what I did until I got prescribed ivabradine. In context ↗

Ask Miruvor AI

Asking aboutPebble 68032’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