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Penelope Fleming

Brianna Fleming / FOXG1 Fundraising Teams

The FOXG1 Research Foundation is tirelessly searching for a cure for FOXG1 syndrome. Their groundbreaking research holds the promise of a better tomorrow for all FOXG1 babies. By donating, you'll be directly supporting the scientists working on treatments that can improve the lives of our children.

To learn more about FOXG1 Syndrome, visit foxg1research.org. Together, we can make a difference!

  • $1,059

    Raised

  • $2,000

    Goal

  • 8

    Supporters

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About Penelope Fleming

Penelope is a firecracker! Though her journey began with a challenge – FOXG1 syndrome – her spirit is bright and determined. At just two months old, she had her first seizure, and after a year of doctor visits and tests, we received her diagnosis. That first year was a whirlwind of hospitals, therapies, and doctor's appointments. It was a scary time, filled with unknowns about what the future held.

Now, at four years old, Penelope is a ray of sunshine. Her smile is contagious, and her dance moves are legendary! She thrives on connection and loves showering everyone she meets with hugs and kisses. Penelope's strength and happiness inspire us every day.

Because of the FOXG1 Research Foundation, there is hope for a brighter future for Penelope and others like her. To everyone who donates to our fundraising team, a heartfelt thank you! Your generosity helps fuel groundbreaking research that will improve the lives of children with FOXG1 syndrome.

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