Low Battery Club
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 connect with me: 🪫tiktok [https://www.tiktok.com/@lowbatteryclubpod] 🪫instagram [https://www.instagram.com/lowbatteryclubpod] 🪫youtube [https://www.youtube.com/@lowbatteryclubpod] 🪫email me [lowbatteryclubpod@gmail.com]! 🪫anonymous form (share your story!) [https://docs.google.com/forms/d/e/1FAIpQLSdJy4dhn8kIHVA5I1K9Le-VEU_VAym5-b_0nwnJROPKSB9NXg/viewform?usp=sharing&ouid=112541262586513689573] 🪫guest application (be on the pod!) [https://docs.google.com/forms/d/e/1FAIpQLSdwaGsf1y_6A0pyvO9juks262n7nqAzZJXPLlU2S9Q3XkOokg/viewform?usp=publish-editor] a little note: if you enjoyed this episode, don’t forget to subscribe and leave a review— it helps more people find the show! 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.
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