Our family conference is the only one of its kind in the world. We offer lectures from the top experts in the field on the latest in research and treatment options, as well as individual clinic appointments with our multidisciplinary team of expert specialists who provide an informal diagnosis and treatment plan to every individual and family. Our conference serves individuals with any type of vascular birthmark, anomaly or syndrome including hemangiomas, port-wine stain birthmarks, lymphatic malformations, arteriovenous malformations, venous malformations, KTS, PHACES, CLOVES, CMTC, and Sturge-Weber Syndrome, among all others. Traditionally held in October, due to the COVID-19 pandemic, the 2020 Vascular Birthmarks Foundation will be a hybrid-conference. We are pleased to offer our individuals and families the opportunity to view our lecture series virtually in 2020.

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