We are more than happy to support individuals and families from around the world.
There are many Ectodermal Dysplasia support organisations already set up in many countries. Please see below for the countries who currently have a support organisation.
If there is not a support organisation in your country and you would like to form one, please contact us and we will be very happy to help you.
The ED International Community Leaders have joined together as a Committee and hold meetings every 18 months to work together in bringing awareness of Ectodermal Dysplasia and to share information and research project news worldwide
(Click on the Country for access to their website)