When we had our daughter Morgan, in 1999, we were perplexed by a strange mark on her face that was soon diagnosed as a type of vascular birthmark called a Hemangioma.

We did our research and soon discovered the Vascular Birthmarks Foundation. Like thousands of families dealing with vascular birthmarks, the VBF was able to aid the us in providing support, information and treatment options for our daughter.

It was through this connection that we decided to form the Frank Catalanotto Foundation.  Our goal has been to raise money and awareness to help support the Vascular Birthmark Foundation.  We are proud to be the honorary chairpersons for the foundation, to help in their efforts to promote the VBF and get the word out about what we are and how we can help. We urge you to become part of our team.

Together we can "Hit a Home Run" to fight vascular birthmarks and be victorious for every child or adult diagnosed with one.