👋 NOTICE

Greetings! You have reached Team Myla Tavilla's 2024 Sprint4Syngap page. If you'd like to donate to her 2025 campaign, please use this link to donate: 

https://www.classy.org/team/635187

Thank you for supporting Myla and SynGAP Research Fund! 

Sweet Myla Tavilla was born with a rare genetic disorder called SYNGAP1. Symptoms include developmental delays, intellectual disability, epilepsy, autism, sensory processing disorder and more. There's currently no cure. We hope to help change that! Our family is participating in #Sprint4Syngap, raising funds for the SynGAP Research Fund (SRF), an organization that works tirelessly to improve the future for kids like Myla. Won't you join us? Thank you for any contribution you can make; all donations go directly to research. And while this is a virtual fundraiser, for those local to Boston, please join us in person! We'll meet on Sat., April 27, 12 pm, at the playground at Fiske School, 55 Adams St., Lexington, MA. All details at tavilla.news/sprint.