We are an international charitable organization networks those affected by a vascular birthmark, anomaly, tumor or associated 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 a vascular birthmark
Here you will find information and resources for patients and families affected by hemangioma, port wine stain birthmarks, arteriovenous malformations, capillary malformations, lymphatic malformations, Sturge-Weber Syndrome, Klippel-Trenaunay Syndrome (KTS), and any other type of vascular birthmark and syndrome.
Join the 2020 VIRTUAL VBF Walk / Run by Signing Up for the 5th Annual Purple Polka Dot Race Today! The Purple Polka Dot Race…Read More
Join the Frank Catalanotto Foundation for the 10th Annual Frank Catalanotto Foundation Golf Classic Two great foundations coming together for the greater good of birthmarks!…Read More
5th Annual Purple Polka Dot Race and Family Fun Run August 9, 2020 Eastwood Beach at Stony Creek Metropark in Shelby Township, Michigan Link to Register: https://purplepolkadotrace.com/race/ The 5th…Read More
Awareness through education is our mission. For our Month of Awareness this May, we are offering full access to our online course: A Foundation in Vascular Anomalies, for only $20.
Medical providers can earn up to 16 CME and others can learn about all types of vascular birthmarks, anomalies, and related syndromes through the first-ever online course in vascular anomalies, written by our team of experts.
After adding the course to your shopping cart, just use code “VBFAWARE” to deduct $79 from the price, making the total upon checkout only $20.
Presenting Dr. Linda's VBF Fact of the Week! Learn from our new VBF weekly educational series with VBF President & Founder Dr. Linda Rozell-Shannon, Ph.D.…Read More
Hi, my name is Michelle Lai and I am 24 years old. I never understood my condition growing up, but I was fully aware of…Read More
My name is Michaeline Tejeda, I go by Lina Dejesus. I am a Cosmetology 22-year-old student who was born with a vascular birthmark on my…Read More