In April 2021, I was diagnosed with POTS, also known as Postural Orthostatic Tachycardia Syndrome. It completely derailed my life plans and I was forced to figure out how to adapt to my new normal. As a journalist at heart, I'm constantly searching for new information and ways to heal, so I figured I'd share my journey with others to help those in a similar position, while also bringing more awareness to this debilitating condition. I've since made great progress with my symptoms and included some resources below!
A quick summary about Postural Orthostatic Tachycardia Syndrome
I've seen a crazy amount of improvement since removing the 'Foods to Avoid for Healing Chronic Illness'
Have you heard of BVD? Many POTS patients also unknowingly have it.
A list of doctors that I currently see and have seen for POTS
A list of medications and supplements that I take to manage my symptoms
A full detailed experience of my trip to the Mayo Clinic, including my final thoughts and tips on getting an appointment
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✨ DISCLAIMER: I am not a licensed medical professional. The content on this website reflects my personal experiences and should not be considered medical advice. I share my journey in the hope that it may inspire and inform. Please consult with a qualified healthcare professional for personalized guidance.