"Welcome to our new look web site. We hope you find it useful. If there is anything you can't find please use our Contact Us page to contact us via either email, telephone or post."

What is EDS?

Ehlers-Danlos Syndrome (EDS) is the name given to a group of heritable connective tissue disorders. EDS can affect the skin, ligaments, and internal organs. More Complete information can be found on our Medical Information page.

What is the Ehlers-Danlos Support Group?

We are a Registered Charity (No. 1014641) and our Group is run by ordinary men and women like you, most of whom have EDS, and some who simply wish to help.

EDS Website.

This website has many purposes; to share medical information about EDS, to make you aware of various support groups and events available, to give you the latest research on EDS, some advice on how to cope with living with EDS, show available publications, and to allow you to discuss your personal issues on EDS with other people in our interactive Message Board.

Message Board

Click here to access the message board. Please register yourself a username to take part in it.

Pictures

We are in the process of adding a few pictures to the website. The first you will see above, a drawing by a volunteer artist Joyce Crocker. Her husband has eds-h and is a member of this site. Thank you Joyce for all your efforts.