|Sturge-Weber International Registry - we are requesting your particiption now - READ MORE
Since 1987, The Sturge-Weber Foundation has been providing superior support and learning opportunities to all individuals and healthcare providers impacted by a port wine birthmark and related conditions such as Sturge-Weber syndrome and Klippel-Trenaunay. The 10 Sturge-Weber syndrome Centers of Excellence around the country provide clinical care and research into new treatments while we search for the cause and cure.
We're a phone call away, 800-627-5482!
For those of you just beginning your search for answers - In the midst of all the challenges, there are many individuals and families who have experienced successes and shining moments. Read about the good things that have happened and continue to happen in the lives of our members. We invite you to join us.
- Not registered? We invite you to join.
- Not sure? Maybe it was a long time ago that you first found us. Re-connect now.
- Registered members have many benefits, including newsletters, contact information for doctors and families, and invitations to conferences, education days and family events. We welcome all individuals and families who have SWS/PWB or KT or have a concern for someone who has these syndromes.