This page is a collection of resources to help you understand more about dysautonomia, including POTS, and its relationship to EDS. I am trying to include a variety of media, since we all learn differently. Some of the resources are links to foundations dedicated to dysautonomia research, some are articles, some are videos.
Notes and thoughts from the Chronic Pain Partners “Trypped Up by Tryptase: An Update on Tryptase Research at NIH” webinar.
Chronic Pain Partners is a wonderful nonprofit dedicated EDS. Their mission is to “ensure greater understanding of Ehlers-Danlos Syndrome by…
I guess this is sort of “old news,” since the research was published in 2013, but I only heard about…
![Child's pose drawing | By Ambermarquez31 (Own work) [CC BY-SA 4.0 (http://creativecommons.org/licenses/by-sa/4.0)], via Wikimedia Commons](https://lifehypermobile.com/wp-content/uploads/2017/06/bpose21.jpg)
New research published in the Annals of Internal Medicine demonstrates that when implemented properly, some forms of yoga can be…