The Vascular Anomalies Alliance was founded in 2024 by several families in the vascular birthmark community.
We are a non-profit 501 (c)(3) connecting & supporting the birthmark community. We strive to REACH our community by financially supporting advancement in Research, Education, and Advocacy, while creating a safe space and sense of Community where everyone feels like they are Home.
Any donations to VAA will help with creating informative materials, helping a family/person in need of treatment or travel to a procedure for their birthmark, anomaly, or related syndrome, funding school wide educational day about birthmarks, or even sending a doctor or medical student to a training or conference in the field of birthmarks.
We excitedly invite you to explore our website to see what we are all about and how YOU can get involved with us!
Federal Tax ID: 33-1862896
