The ED Society
We are a dedicated UK charity committed to supporting families and individuals affected by the rare genetic condition, Ectodermal Dysplasia (ED). Our mission is to raise awareness, provide comprehensive support and advice, and connect you with leading medical professionals.
We understand the unique challenges faced by those living with ED, and we are here to help. Whether you need guidance on day-to-day management, educational resources, or assistance in liaising with schools to ensure your children receive the proper care and attention they need, we are by your side every step of the way.
Together, we can increase understanding, continue building our supportive community, and improve the quality of life for everyone affected by ED.
Join us in our journey to empower and uplift those living with Ectodermal Dysplasia.
Registration No. 1089135
