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.
Uk private health insurance - worth it or not?
Is this definitely hereditary? 
Confused over diagnosis!
Pregnancy and Ehlers Danlos Type 3
