What We Wished We'd Known When We Were First Diagnosed || Dysautonomia Awareness Month

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's videos is mainly for people who are undiagnosed or newly diagnosed. We talk about all the things we wish we'd have known when we were first diagnosed with POTS and we hope if you know some of these things early on it might make your journey that little bit easier.

For more information on POTS & Dysautonomia please head to:
potsuk.org or dysautonomiainternational.org


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Meet my Dysautonomia Warriors:

Izzy Kornblau - New York, USA.
instagram.com/izzykornblau


Mikki - Holland.
instagram.com/potsiewotsie

Holly - New Zealand.
instagram.com/hollyhoneey

Sophie - UK.
instagram.com/thesophieproject_

Amy, UK.
instagram.com/amyruthnorris

Hailey, Ohio, USA.
Instagram.com/hailhailfail


Music Credit:

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