The SWSCC is a branch of the Vascular Birthmarks Foundation. If you would like to make a donation to VBF, please send a check made payable to

PO Box 106
Latham, NY 12110

All donations are greatly appreciated as without your help we cannot continue to help families.

To donate by credit card, please visit VBF's site.


mission statement

The Sturge-Weber Syndrome Community, a branch of the Vascular Birthmarks Foundation, provides support and services freely and upon a volunteer basis for individuals and families living with SWS and vascular birthmarks, while sponsoring research and promoting physician education and awareness, as well as education of the public at large.