The Fundraising committee helps our community raise donations for VBF through online and in person events, which goes directly towards our mission of networking those affected by a vascular birthmark, anomaly or related syndrome (VBARS) to the appropriate medical professionals for evaluation and possible treatment. The Vascular Birthmarks Foundation educates physicians and affected families regarding treatment options, supports relevant research, mobilizes medical missions, and empowers those living with vascular birthmarks.

One in every ten babies are born with a vascular birthmark, anomaly, or related syndrome, yet many children and adults lack an accurate diagnosis and treatment plan that can save lives. VBF has networked over 125,000 patients in 6 continents, over 150 countries, and in all 50 states within our 28 years of history. Donations can help transform these lives, one birthmark at a time. These funds go towards many initiatives, but the main event is our annual conference and clinic. This conference brings together patients and their families with the world’s leading physician experts on vascular anomalies from around the world. The VBF is the only charitable organization for birthmarks that provides free hotel accommodations, meals, conference admission, and clinic appointments to families affected. There are several fundraisers that take place each year to provide support towards our mission such as the Purple Polka Dot Race, Wishlist by AM Fashion Show, Enchanting Magic by Nick, Give2MyVBF, Facebook Fundraising and more!