The POTScast E180: Emily from Washington, a medical assistant who developed POTS

Emily was working as a medical assistant when she developed POTS. While she was aware of POTS, receiving a proper diagnosis still took 7 or 8 months. Many practitioners were dismissive of her symptoms, leading to a delay in treatment. 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.