Stepping Together for a Breakthrough!
Each year, hundreds of community members mobilize for our Walk ‘n’ Wheel to raise awareness of Lennox-Gastaut Syndrome and raise crucial funds for the LGS Foundation’s “Finding the Cures, Together” Research Program.
With only a tiny fraction of public and private funds going towards research on LGS, families of the more than one million people with LGS worldwide worry that lifesaving, stabilizing treatment may not come to fruition in their loved one’s lifetime. We are here to change that!
You won’t want to miss our 10th Annual Walk ‘n’ Wheel for LGS Research!
Save the Date | April 26th, 2025
Tampa, Florida
Walk Where You’re At!
Leesburg, Virginia
get involved Now!
GIVE NOW TO SUPPORT LGS RESEARCH
All proceeds benefit the “Finding the Cures, Together” Research Program. This vital program drives cutting-edge, patient-led research that leads to new therapies and treatments for those impacted by LGS! You can help too! We hope you’ll join us!
This Walk ‘n’ Wheel event is made possible with support from our friends at:
Bronze Level
Thank you supporting our
8th Annual Walk 'n' Wheel for LGS
With your help, we've raised over $44k for LGS Research, putting us at 73% of our $60k goal.
Keep the momentum going! There is still time to be part of funding life changing research.
The LGS Foundation held its 7th Annual Walk ‘n’ Wheel for Lennox-Gastaut Syndrome on March 26th, 2022 to raise awareness and increase funding to accelerate research on Lennox-Gastaut Syndrome (LGS), a rare and often debilitating form of early-onset epilepsy. Approximately 1,000,000 children and adults worldwide have LGS.
The 2022 annual #WalkForLGS raised over $48,000, nearly 78% of our $60k fundraising goal!
Although great strides have been made, more work needs to be done.
We are not done yet…
With only a tiny fraction of public and private funds going towards research on LGS, families of the more than one million people with LGS worldwide worry that lifesaving, stabilizing treatment may not come to fruition in their loved ones lifetime. The LGS Foundation’s Cure LGS 365 Research Grants Program is combating these fears.
Hundreds of LGS families and community members came together on June 5th, 2021 to Step Towards a Cure for LGS! Together our community pledged Over 1 Million Steps and Raised Over $60,000 for Research into Lennox-Gastaut Syndrome.
Watch the 2021 Walk Video
Updated 01/15/25 (KK)