The Vascular Birthmarks Foundation

Dr. Linda Rozell-Shannon, PhD President and Founder

We are here for you.

You may post questions and/or concerns on our VBF Facebook page or email us. Listed below are Facebook pages and groups that may be appropriate for the vascular birthmark type that you or a loved one has been diagnosed with. The following are some examples but do not represent an exhaustive list. You can google the name of the various vascular birthmarks/anomalies types and find many closed and open groups which encourage discussion. VBF also monitors some groups to provide information to affected individuals and families.

Additionally, we offer a variety of support programing throughout the year. Interested in learning more? Email Emily at emily@birthmark.org


The Vascular Birthmarks Foundation

Main site

VBF Global Ambassador Program

Ask / Accept: Anti-Bullying Campaign

Parent Advocacy Network

Others

General Support

Hemangiomas

Port Wine Stains

Venous Malformations

Arteriovenous Malformations

Lymphatic Malformations

PHACE Syndrome

Sturge Weber Syndrome

Klippel Trenaunay Syndrome

CMTC Cutis Marmorata Telangiectasia Congenita

MLT/CVAT – Multifocal
Lymphangioendotheliomatosis with Thrombocytopenia