Скачать или смотреть Preparing for Laser Treatment in SWS Port-Wine Birthmarks

In this episode of The Sturge-Weber Foundation's "What's Your Plan" Series, Dr. Kristen Kelly from the University of California Irvine discusses Port-Wine Birthmark Laser Treatment for Sturge-Weber Syndrome Patients.
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The SWF was founded by Kirk and Karen Ball. They began searching for answers after their daughter, Kaelin, was diagnosed with Sturge-Weber syndrome at birth. The SWF was incorporated in the USA in 1987 as an International 501(c)(3) non-profit organization for patients, parents, professionals, and others concerned with Sturge-Weber syndrome (SWS). In 1992, the mission was expanded to also support and serve individuals with capillary vascular birthmarks, Klippel-Trenaunay (KT), and Port-Wine Birthmarks.

To learn more or make a donation to advance research visit: www.Sturge-Weber.org

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