We are constantly on the lookout for new resources that might be available for affected SWS families and patients. Here is a list below you may find useful.
KT Foundation: https://www.facebook.com/ktfoundation/
K-T Support Group: https://k-t.org/
Sensory Integration Network: http://www.sinetwork.org/
Sturge-Weber UK: http://www.sturgeweber.org.uk/
Pediatric Glaucoma & Cataract Family Association: http://pgcfa.org/
Vascular Birthmarks Foundation: https://birthmark.org/
VBF Europe: http://vbfeurope.org/
The Hemispherectomy Foundation:http://hemifoundation.homestead.com/welcome.html
