The Sturge-Weber Foundation (SWF) is a non-profit foundation serving people with Sturge-Weber syndrome (also known as encephalotrigeminal angiomatosis), Klippel Trenaunay (KT) and Port Wine Stains (PWS), their families, and the medical and professional community. The Foundation acts as a clearinghouse for information and to facilitate fund raising for research into SWS, KT and PWS. The Foundation provides telephone counselling in addition to an e-mail support group on the Internet
Articles, pamphlets and booklets on Sturge-Weber syndrome. SWF: The Sturge-Weber Foundation Newsletter--periodic, articles on treatment, medical updates, and information relating to Sturge-Weber syndrome.
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