
09/01/2025
đ Ever stand up and feel like your heart is sprinting while youâre standing still? Add dizziness, brain fog, fatigue, and itâs not just âin your head.â For many, this is POTS (Postural Orthostatic Tachycardia Syndrome)âand itâs now recognized as one of the most common complications of long COVID.
In my latest post, I dive into:
⨠How COVID can trigger POTS and other dysautonomias
⨠Why women are most affected
⨠What it actually feels like (spoiler: not fun)
⨠Current treatment approachesâwhat helps, what doesnât
This isnât just an odd footnote of the pandemicâitâs a growing reality for thousands still struggling to return to ânormal.â In the past 5 years I have seen an uptick in cases. Just last week, I saw two new patients with dysautonomia! The diagnosis is not hopeless, despite likely being told drink more water and take salt pills, there is more you can do! When treatment options are limited, sometimes we have to step outside our comfort zone and explore new strategies. Living with POTS or dysautonomia after COVID often means thereâs no quick fixâso itâs about trying different approaches, layering lifestyle shifts with supportive therapies, and being open to options that might feel unfamiliar at first. Itâs in that spaceâoutside of what feels easy or routineâthat many patients start to discover what actually helps.