The Sturge-Weber Foundation is continually offering programs and events for patients and their families to learn more, get to know other families, and just have fun!
Held alternate years around the country, this conference brings together families and dedicated clinicians and scientists to improve the quality of life for those affected by Sturge-Weber syndrome and Port Wine birthmark conditions.
Education Forums and Local Family Days
Educational Forums bring together families and dedicated clinicians on a smaller scale than the International Conferences. Local Family Days offer an opportunity to meet others in your area. Interested in hosting a Family Day? Contact Anne at firstname.lastname@example.org.