The Vascular Birthmark Foundation is an international charitable organization that networks families affected by a vascular birthmark, tumor, or syndrome to the appropriate medical professionals for evaluation and/or treatment, provides informational resources as well as sponsors physician education, mobilizes medical missions trips, and supports research and programs that promote acceptance for individuals with birthmarks.
We invite you to browse oursite to find information and resources for patients and families affected by hemangioma, port wine stain, arteriovenous malformation, capillary malformation, lymphatic malformation, Sturge-Weber syndrome, Klippel-Trenaunay syndrome, and any other type of vascular birthmark and syndrome.
The Vascular Birthmark Foundation has been making a difference for those with patients and families affected by vascular birthmarks and related syndromes for over 25 years.
The Vascular Birthmarks Foundation
PO Box 106
Latham, NY 12110