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, the foundation provides resources and assistance to patients and families affected by these conditions.
Offering a variety of programs, events, and resources, the foundation supports the community and raises awareness about these rare neurological and ophthalmological conditions. They also conduct research, provide opportunities for professionals to engage in the field, and offer ways for individuals to get involved through fundraising, volunteering, and becoming Legacy Leaders to support the foundation's mission.
Generated from their business information