Welcome to the Ehlers-Danlos Support UK community!
The point of this community is to provide a space where you can share your experience, support one another and become better informed about Ehlers Danlos Syndrome ("EDS").
This community is intended to supplement the services and information provided by the EDS UK charity (ehlers-danlos.org).
Please feel free to start commenting, blogging and asking questions about anything relating to how EDS affects your life and we'll do our best to respond as quickly as possible.
Endometriosis and EDS/HEDS?
This is all new to me.
Should I go to the doctors with these symptoms 
