today is the day: i’m finally sharing my full journey with postural orthostatic tachycardia syndrome (POTS).

in this episode, i break down everything—from what i believe triggered it, to the strange early symptom that stumped every doctor, to the long road to getting diagnosed. i also open up about the emotional side of living with a chronic condition like this.

whether you think you might have POTS, have already been diagnosed, or care about someone who has it, i hope this episode helps you feel more informed—and less alone.

living with POTS can feel incredibly niche and isolating. my goal with this episode is to make that experience a little more understood🤍

topics (with timestamps):

00:56 a huge misconception about POTS

07:51 what triggered my POTS

12:13 non-epileptic seizures

18:20 my POTS symptoms

20:31 getting misdiagnosed

23:33 POTS testing + diagnosis

26:47 the emotional side of dr’s appointments

28:42 what it felt like getting diagnosed

32:10 my current medical mystery

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disclaimer: the information shared on this podcast is for educational and informational purposes only and should not be considered medical advice. the host is not a licensed medical professional.

always consult with a qualified healthcare provider before making changes to your diet, supplements, medications, or health routines.