For nearly 30 years of my life I was unaware that the vascular malformation on my left leg had a name, or that there were others with similar stories and experiences. It wasn’t until I found the Vascular Birthmarks Foundation, that I learned that I was born with Klippel-Trenaunay Syndrome affecting my left leg.
I am fortunate that KTS has not prevented me from living an active and wonderful life, although it is something that is a part of my everyday experience. I think my birthmark makes me unique and I hope that I can share that message with others. It is an honor to be an Ambassador for VBF.