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Long COVID Severe → somewhat betterIll 3 years before improving or writing

Long COVID with chest pain and GI problems, somewhat better with a treatment cocktail

Condition
Long COVID
At worst
Severe (mostly bedbound)
Ill before improving or writing
3 years
Last post
Jul 2025
In their words
  • Condition: Long COVIDGoing on 3 years of a brutal case of long covid In context ↗
  • At worst: Severefelt like a broken, pointless human for being bedridden all day In context ↗
  • Now: Somewhat betterI’m starting to see glimmers of who I used to be In context ↗
  • Began after: COVIDnot getting sick for 3 years since my covid infection
Read from 5 of their posts and comments; links to the 4 this page draws on

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Summary

Trail 49897 has had long COVID for about three years, with chest pain, GI problems and a six-month stretch when symptoms were so bad they considered whether life was worth living. A cocktail of extended-release pyridostigmine, ivabradine, LDN and digestive enzymes, plus a routine and work on mental health, brought slow glimmers of their old self. A concussion set them back badly, and three months later they were only slowly returning to their long-COVID baseline.

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What they tried

Also tried

oatmeal· HelpedPanplex 2-Phase digestive enzymes· Helpedpsyllium fiber· WorseniaCEL· Worse
Their words about each treatment
  • psyllium fiber · WorseI've tried multiple times over the years, at varying ramp-ups ... and I always feel off, bloaty, or just plain worse than before. In context ↗
  • oatmeal · Helpeda warm bowl of oatmeal (or cold cereal with oat milk) in the morning daily does wonders. It's helped me maintain a decent fiber intake without all the side effects In context ↗
  • niaCEL · WorseI have a mild intolerance to niaCEL In context ↗
  • extended-release pyridostigmien · HelpedI finally have a good cocktail of meds that includes extended-release pyridostigmien, ivabradine, LDN, and Panplex 2-Phase digestive enzymes In context ↗

Approaches: POTS medication

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 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
2022long COVID after covid infectionGoing on 3 years of a brutal case of long covid In context ↗Not stated
2022-2023six months of severe symptoms, bedridden, suicidal thoughtsmy symptoms got so bad for six months that I was starting to really consider whether or not it was worth being alive anymore In context ↗Severe
2025-07-11good med cocktail and routine, glimmers of old selfI finally have a good cocktail of meds that includes extended-release pyridostigmien, ivabradine, LDN, and Panplex 2-Phase digestive enzymes; I’m starting to see glimmers of who I used to be In context ↗Moderate
2025-04set back for months by a concussioneven a mild-moderate concussion recently set me back horribly symptom-wise In context ↗Severe
2025-07-16slowly returning to long-COVID baseline after concussion3 months later, things are slowly getting by back to my LC normal. In context ↗Moderate

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Heart symptoms & palpitationsthe first emergency room visits for chest pain In context ↗
  • Gut problemsI was somehow puking my guts out and going to the bathroom at the same time because of the GI issues In context ↗
  • Anxiety & low moodI was starting to really consider whether or not it was worth being alive anymore In context ↗

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