💓 Zebby's POTS

Your heart's not broken. Your autonomic system is improvising.

POTS, dysautonomia, and the trifecta.

Zebby's POTS is for everyone living with Postural Orthostatic Tachycardia Syndrome — the standing-up disorder that gets dismissed as anxiety more often than it gets diagnosed. The dysautonomia community is your people. So is everyone with EDS + POTS, MCAS + POTS, or post-viral POTS.

We cover what the dysautonomia research actually says (Dysautonomia International is a gold standard source), the salt + fluid + compression baseline that almost every POTS doctor agrees on, the pacing techniques that work, and what to bring to the cardiologist when you're advocating for a tilt-table test.

We don't prescribe. We don't recommend salt amounts, fluid amounts, or supplements — talk to your care team. We surface what's known, what's debated, and what spoonies who've had this for years actually do.

What we cover

Sources we trust

Spoonie-validated lifestyle picks

What the community actually uses

Compression socks (15-20mmHg, knee-high)

~$25

The first POTS intervention most doctors recommend. Get a few pairs.

See on Amazon →

Insulated water bottle 32oz

~$30

You need water within arm's reach all day. This one holds ice for 24h.

See on Amazon →

Recliner cushion / wedge

~$45

Sleeping with head elevated is part of the POTS toolkit.

See on Amazon →

Affiliate links — small commission, no extra cost to you. These are lifestyle items only, not medical recommendations. Talk to your care team about your specific case.

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