The POTScast E176: Hanna from Oregon, museum educator who waited 15 years for diagnosis

Hanna had a 15-year journey to her POTS diagnosis after fainting episodes that started in her teens. An avid athlete, she has completed a triathlon and climbed mountains in her less symptomatic days. Standing Up to POTS is a non-profit organization dedicated to improving the quality of life for people with postural orthostatic tachycardia syndrome (POTS) through research, advocacy, and support. If you like this video, please subscribe to our channel! Find out more about Standing Up to POTS! Check us out on our Website: www.standinguptopots.org Facebook:   / standinguptopots   Instagram:   / standinguptopots   Twitter:   / potsactivist   Pintrest:   / thestandinguptopots   Medical Disclaimer: The information provided here is not intended to serve as professional medical advice, diagnosis, or treatment. If you have health related issues, please contact a qualified health professional to get the personalized assessment, advice, and treatment that you need. Standing Up to POTS will not be liable for any direct, indirect, or other damages arising from the use of this video.