This cause is deeply personal to me. My son Mykhailo (Misha) is 7 years old and lives with FOXG1 syndrome. Like many FOXG1 children, he faces challenges every day, but he continues to amaze us with his progress, his personality, and his determination. I’m fundraising for Misha and for all the incredible children and families living with FOXG1 around the world.
The FOXG1 Research Foundation is a parent-led nonprofit driving a historic effort to bring the first-ever treatment for FOXG1 syndrome — a potentially life-changing gene therapy — to children around the world.
And right now, every dollar raised is matched dollar for dollar, up to $1,000,000!
Here’s how you can help:
Donate: Every dollar helps, and right now every dollar is doubled!
Share: Spread the word by sharing this page.
Start a Team: Create your own page and join the Million Dollar Match before December 31!
Thank you for supporting Misha and the FOXG1 community, and for being part of this incredible movement.