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This year I have brought together a fabulous group of Dysautonomia Warriors from 4 different countries across the world to talk all about Dysautonomia for Dysautonomia Awareness Month. We all live with POTS ( Postural Orthostatic Tachycardia Syndrome) which is a dysfunction of the autonomic nervous system and causes high heart rates, low blood pressure and many other symptoms. This October we will be bringing you lots of videos sharing our lives with POTS to help fellow sufferers and help the rest of the world understand what living with these chronic conditions is really like! This week we are talking all about our diagnosis stories; how we were diagnosed, who by, and how long it took. For more information on POTS & Dysautonomia please head to: potsuk.org or dysautonomiainternational.org If you liked this video please subscribe to my channel :) You can also find me on other social media: Facebook: / chronicallyjenni Instagram: / chronicallyjenni Twitter: / jennipettican Facebook support group: / 785786465114178 Mixcloud: https://www.mixcloud.com/jenni-pettican/ Email: [email protected] Buy Me A coffee: buymeacoffee.com/chronicjenni Kit: https://www.kit.com/chronicallyjenni Blog: https://www.chronicallyjenni.com Meet my Dysautonomia Warriors: Izzy Kornblau - New York, USA. instagram.com/izzykornblau / @izzykdna Mikki - Holland. instagram.com/potsiewotsie Holly - New Zealand. instagram.com/hollyhoneey Sophie - UK. instagram.com/thesophieproject Music Credit: https://www.bensound.com/royalty-free...