Support

Please join our online discussion/support groups.

Public Group

Sturge-Weber Syndrome Community Support at MSN Groups

SWSC Support at ©MSN Groups is open to the public. If your child has SWS, or if you have SWS, are a family member, a friend, or just want to learn more about SWS, this group is for you. The group also hosts weekly SWSC Chat Sessions.

Private Group

SWC Talk Community Individuals Group at Yahoo Groups

The SWC Talk Community Individuals Group at © Yahoo Groups is for Individuals with SWS only. You must be least 16 years old to apply, and can also register for membership to our website SWSC Individuals Group.

If you have any questions regarding group membership, please contact the SWSC Support Group Manager at: swsc@swscommunity.org

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.

The SWSCC is a Chapter of the Sturge-Weber Syndrome Community (US), a Branch of the Vascular Birthmarks Foundation.

VBF is a fully approved not-for-profit. Your donations are tax deductible.
Federal Tax ID 16-1515227

Always seek the advice of a physician or other medical professional for diagnosis and treatment. The SWSC and/or VBF are not responsible for the content or accuracy of any information, advice or links on the site.