Mission Statement: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.
Here you will 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.
Social media links: https://www.facebook.com/VascularBirthmarksFoundation https://twitter.com/VBirthmarks https://www.instagram.com/vbirthmarks/ https://www.youtube.com/user/VBFchannel?feature=watch
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