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What helps others — with Long COVID, ME/CFS & POTS

People with Long COVID, ME/CFS and POTS log what they tried and how they felt afterwards. Here you can see what went together with better values across many people. Everything is pseudonymous. This is an observation, not a recommendation.

Illustration: a gentle web of glowing, connected dots symbolizing a supportive community

No one is individually identifiable. Only the shared pattern counts: numbers appear only from at least 10 people per group.

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Join in — the more people, the clearer the patterns.
Everything here comes only from voluntary, pseudonymized data. Nothing is passed on to external companies — it's used solely to improve mypacing. Figures only appear once enough people have contributed that no one is identifiable. The more of your own data you add, the sharper the patterns become — for you too.
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Important: A lot of what appears here (e.g. medications) is off-label or experimental. Always discuss with your doctor whether something is right for you. Correlation is not causation — what helped many people may work differently for you.
What is known about pacing apps — including the uncomfortable part.

We write down here what research says about applications like this one. Including where it speaks against us.

What that means for mypacing. mypacing records and shows. It does not predict, it does not detect illness, and it does not promise to prevent crashes. What follows from what you see here is your decision — on your own, or with your doctor.

mypacing is not a medical device and does not provide a diagnosis. All figures are aggregated, pseudonymous self-observations (minimum group size, k-anonymity) — not a study, not a treatment recommendation. In an emergency, call your local emergency number. · © 2026 mypacing · Stay at your own pace. mypacing is a trademark application on file with the German Patent and Trade Mark Office (DPMA), Ref. No. 302026242304.3.