Vascular Birthmarks Foundation

**The Vascular Birthmarks Foundation** **Dr. Linda Rozell-Shannon, PhD President and Founder** Over 150,000 Networked Into Treatment The Vascular Birthmarks Foundation is an international charitable organization that networks families affected by vascular birthmarks, anomalies, and/or related syndromes (VBARS) 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 our site 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 Birthmarks Foundation has been making a difference for those with patients and families affected by vascular birthmarks and related syndromes for over 30 years. **Vascular Birthmarks Foundation, PO Box 106, Latham, NY 12110** An international charitable organization that networks families affected by a vascular birthmark, anomaly, or related syndrome to the appropriate medical professionals for evaluation and/or treatment, educates physicians and affected families regarding treatment options, supports relevant research, mobilizes medical missions, and empowers those living with vascular birthmarks. The Vascular Birthmarks Foundation is a 501(c)3 charitable organization - Federal Tax ID 16-1515227