WEB RESULTS

https://sturge-weber.org/

We exist to improve the quality of life and care for people with Sturge-Weber syndrome and associated Port Wine Birthmark conditions. We support them with  ...

https://sturge-weber.org/new-to-swf/understanding-sturge-weber.html

Whether you or your child has been newly diagnosed with SWS or KT, or if he/ ...

https://sturge-weber.org/for-patients/swf-clinical-care-network.html

The Centers of Excellence has expanded to the SWF Clinical Care Network ...

https://sturge-weber.org/new-to-swf/types-of-sturge-weber-syndrome.html

The most apparent indication of Sturge- Weber Syndrome is a facial birthmark or " ...

https://sturge-weber.org/participate/ways-to-give-to-swf.html

It is through the generosity of our donors that our work is made possible. We ...

https://sturge-weber.org/who-we-are/mission.html

The Sturge-Weber Foundation is a 501 ( c) (3) non profit organization with an ever ...

https://sturge-weber.org/for-patients/our-research.html

SWF RESEARCH UPDATE FROM KAREN BALL June 18, 2018. When The  ...

https://sturge-weber.org/for-professionals/swf-research.html

Jan 24, 2018 ... Translational research is when biological insights are gained ...

https://rarediseases.org/the-sturge-weber-foundation/

Sep 8, 2015 ... Established in 1987, the Sturge-Weber Foundation is dedicated to acting as a clearinghouse for information on all aspects of port wine stain ...

https://rarediseases.org/organizations/sturge-weber-foundation/

The Sturge-Weber Foundation (SWF) is a non-profit, 501(c)3 organization for parents, professionals, and others concerned with port wine stains, Sturge-Weber  ...