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CONTACT THE SWSCCSWSCC / CCSSW Email: If you need further help or additional information, please email us with your name and phone number and we will be glad to call you, or you can fill out and submit the form below. Visit our on-site Discussion Board and our other Online Support Groups .
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mission statementThe 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. |
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Copyright © 2003-08 Sturge-Weber Syndrome Community. All Rights Reserved. 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.
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.
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