Thank you so much for visiting my page.

Family means so much to me as I'm sure it does to you too! The Board of Directors and I are leading the way to support vital research for Sturge-Weber syndrome and Port Wine Birthmark conditions through the SWF Million Miles campaign.

Kaelin Ball, my daughter, was born with Sturge-Weber syndrome and is the catalyst for the beginning of the Foundation. 

We hope to make a huge impact this year, but we need your help! Please consider donating to this special campaign.  No contribution is too small!