I consider myself very lucky to have been diagnosed with POTS within less than 1year from the onset of symptoms, and through the first doctor I met with. Not many healthcare professionals know how to help with POTS, or even what it is. I’m hoping to be able to help spread awareness about POTS and Dysautonomia through my account, as well as share my journey through the trial and error process of other diagnoses as well as potential treatments. Source: https://www.dysautonomiainternational.org