The Sturge-Weber Foundation is a global organization dedicated to improving the quality of life and care for individuals with Sturge-Weber syndrome and associated Port-Wine Birthmark conditions. Through collaboration with clinical partners, education, advocacy, research, and support, they strive to make a positive impact on the lives of those affected by these conditions.
With a focus on unity and progress, the foundation brings together individuals from around the world to support and empower those with Sturge-Weber syndrome. They offer resources, information, and support to patients, families, and professionals, while also investing in important research and awareness efforts. By becoming a Legacy Leader, supporters can contribute to the foundation's mission and help create a brighter future for generations to come.
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