Our Mission
The Sturge-Weber Foundation (The SWF) global mission is to improve the quality of life and care for people with Sturge-Weber syndrome and associated Port-Wine Birthmark conditions through tenacious collaboration with clinical partners and pioneers, education, advocacy, research and friendly support. Learn more and get involved.
What's New In Research
Early MRI diagnosis of Sturge Weber Syndrome type 1 in infants
Read more news at Science Direct, keyword search Sturge-Weber.
The Official Sturge-Weber Foundation Twitter
‘She’ll never have a boyfriend!’ My dad rushed out of the room. It looked like I’d been punched in the cheek.’: Rea… https://t.co/dWMV2OdkJl
MUST SEE TV: 'Dr. Pimple Popper' Season 8: Dr. Lee treats Eddie's port-wine stain to help him get back into the wor… https://t.co/969Dskiya2
Sponsor: UCB
The Sturge-Weber Foundation (SWF) provides sponsors the opportunity to share information through our public communication sites. SWF does not endorse, prescribe or recommend any products shown in sponsor information. Please consult your doctor for questions regarding any medical information.
