I’m thrilled to be participating in the Rare Disease Day fundraiser for Kabuki Syndrome Foundation to suppot our daughter Olvia who lives with Kabuki Syndrome. 

This nonprofit drives research to treatments, creates resources for families, and strengthens the global Kabuki syndrome community. Every donation helps me reach my goal and creates healthier futures for our loved ones with Kabuki syndrome. 

Here's how you can help:

• Donate: Contribute whatever you can. No amount is too small!
• Spread the Word: Share my fundraising page with your friends, family, and social networks. Let’s spread awareness so we can raise more!

Thank you for standing by me, not only today but every day. Please consider donating in honor of Rare Disease Day, February 28, 2026 and all the families impacted by Kabuki syndrome. Thank you.