The POTScast with The Dysautonomia Project

Thanks for making this POTScast for all of us new and clueless people navigating this new adventure 😵‍💫 you have helped me more than any of the multitude of doctors I’ve seen so far!! Keep ‘em coming please!!

For anyone who has POTS or loves someone who has POTS. I have EDS and POTS. My journey has been very difficult. This podcast was incredibly helpful for me (and my mom, who has spent her life undiagnosed) and provided a sense of community. Please bring it back!!

We need you back! People are suffering and the internet isn’t helpful. I have to dig so hard for information.

This podcast has been incredibly helpful! I haven’t finished all the episodes so I might answer my own question in time, but I wanted to know if you’ll be coming out with new episodes in the future.