Medical Advisory Board
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SWSC Canada in French
Ask the SWS Expert
Ask the Eye Expert
Ask the Laser Expert
Ask the Medical Rehab Expert
Ask the Developmental Specialsist
Ask the SWS Nurse
SWS Pamphlet (pdf)
PWS Treatment Guide (pdf)
Find a Doctor
SWSC Support Groups
Join Glen's Gang (for kids)
Please join our online discussion/support 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.
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: email@example.com
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.
Copyright © 2003-10 Sturge-Weber Syndrome Community. All Rights Reserved.
VBF is a fully approved not-for-profit.
donations are tax deductible.
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.