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Dr. Dave Shahani with Cooks Children's Medical Center breaks down the types of seizures and how they are treated. 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 Follow us on Instagram: / thesturgeweberfoundation Facebook: / sturgeweberfoundation Twitter: / sturgeweber The Sturge-Weber Foundation is a 501 (c) (3) non-profit organization © The Sturge-Weber Foundation, July, 2022 Filmed by Karen Images