VBF-Sturge-Weber Syndrome Community

Official chapter of the Vascular Birthmarks Foundation (VBF)

Our VBF-SWS Global Ambassadors have Sturge-Weber syndrome, or are a family member. If you would like to join our Global Ambassador program, please visit our VBF Global Ambassadors page and submit your information. It is the goal of VBF-SWS to have Volunteer Reps in every state and country.

VBF-SWS Representatives volunteer their time to support patients and families living with Sturge-Weber syndrome. VBF-SWS Representatives are not qualified or authorized to give medical advice of any kind. Please consult a physician or medical expert regarding diagnosis, treatments, and all other medical issues related to SWS. 

VBF-SWS Global Ambassadors

For a complete list of VBF SWS Ambassadors, visit our Birthmark Ambassadors’ page.