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 programming throughout the year. Interested in learning more? Email VBF at info@birthmark.org


The Vascular Birthmarks Foundation

Main site

VBF Global Ambassador Program

Ask / Accept: Anti-Bullying Campaign

Parent Advocacy Network

Adults Living With … 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

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