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Guide

POTS & dysautonomia: what a symptom tracker can (and can't) do

If you're here, you probably know the drill: dizzy when standing, heart rate doing things, fatigue that doesn't match the activity that caused it, brain fog with a mind of its own. Tracking can help you advocate for yourself — but only if it stays honest about what it is and isn't.

What a tracker can genuinely do

What a tracker can't do (please don't ghost your care team)

What's actually worth logging

Keep the list tiny or your brain fog will veto the whole project. For POTS folks in particular: heart rate (resting, and after standing for a couple minutes if you can manage it), blood pressure when you remember, fatigue level, brain fog, dizziness, and the weather flare heads-up. That's it. You don't need to log every symptom from a catalogue of 300 — just the ones that rule your life.

Watch for patterns, not perfection

Health anxiety is real, and a tracker can feed it if you let it — refreshing your log like a stock ticker, panicking over every spike, guilt over missed days. The healthy relationship is: log what you can, glance at trends every so often, and hand the evidence to your care team. The tracker works for you, not the other way around.

The honest truth

POTS is a marathon and your energy is precious. Tracking helps when it saves you spoons — when it costs you spoons, dial it back. The goal isn't a beautiful chart. The goal is walking into a specialist appointment with your patterns in your hand instead of your words lost in your fog.

CI Baddies (the app, right over here) has sliders for heart, breathing, dizziness and brain fog, vitals for heart rate and blood pressure, and a weather flare heads-up — all in taps, none of it demanding a perfect record. Built for the hardest days, because that's where you live.