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Hello Bonnie, Full disclosure – I have yet to train in ART. I will this in the next month though! With that, I am responding in this thread because I personally have POTS. Its symptoms have been linked with problems related to vagal nerve dysfunction. Given premise of Polyvagal theory and its relation to trauma, I’d be deeply curious about the outcome of this treatment for individuals with POTS. Good luck! If you choose to proceed, I would be really interested to learn about the outcome. All the best, Jennifer