Olivia Grace’s VBF Story of Hope

May is the Month of Awareness for
Vascular Birthmarks, Anomalies, and Syndromes. 

Watch Olivia’s journey to share her experience living with an intramuscular venous malformation of the leg.  This is how VBF gives hope and makes a difference.

Thanks to our VBF Family, we have networked over 125,000 others into treatment for over 26 years. Together we are #VBFStrong

You can make a gift to VBF in Olivia’s honor:

Click the Month of Awareness badge below to join the movement this May: