The Sturge-Weber Foundation (The SWF) is dedicated to enhancing the well-being and treatment of individuals with Sturge-Weber syndrome and associated Port-Wine Birthmark conditions worldwide. We achieve this through strong partnerships with medical experts, promoting education, advocating for patients, conducting research, and providing empathetic support. We aim to positively impact the lives of those affected and that includes making accessibility a priority.
We are constantly working to enhance the accessibility of our content. If you come across any accessibility issues while browsing our website, we kindly ask you to fill out the Accessibility Barrier Form provided below. Your feedback is greatly appreciated.
Additional web accessibility enhancements are available on this website thanks to our partnership with AccessiBe.