This video for dysautonomia awareness month is for anyone who has been newly diagnosed with POTS. My team of dysautonomia warriors from across the world are here to share their best pieces of advice and words of wisdom with you from what they've learned through their own POTS journeys. These are the things we wish we'd have known when we were first diagnosed with POTS so I really hope you find it useful!

POTS survival Kit: [ Ссылка ]
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Postural Orthostatic Tachycardia Syndrome or POTS is a condition I've been living with for 5 years now. POTS is a form of Dysautonomia (or Autonomic dysfunction) which causes high heart rates and a plethora of other debilitating symptoms. This video lets you know what it's like to live with POTS including symptoms you might expect and how it can make you feel to live with an invisible, complex, chronic illness directly from the people who live with it on a daily basis. Please subscribe as there are still more awareness month videos to come.

People in this video :

Chronically Jenni - instagram.com/chronicallyjenni
Lizzie Draper - instagram.com/ooh.dizzy.lizzie
Rich - instagram.com/mypotsofview
Chersti - instagram.com/okaychersti
Jenny Cole - instagram.com/jennycole1988
Mikki - instagram.com/potsiewotsie
Fern - instagram.com/fern.andforest

If you liked this video please subscribe to my channel :)

You can also find me on other social media:

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