Walk ‘n’ Wheel for LGS Research

Stepping Towards the Cures, Together!

Each year, hundreds of community members mobilize to raise funds for the LGS Foundation’s “Finding the Cures, Together” Research Program. This vital program drives cutting-edge research that leads to new therapies and treatments for those impacted by LGS!

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. We have until May 31, 2023 to reach 100% of our goal.

Give Now to support LGS Research

Log in to your personal fundraising page

*All donations must be made through your individual personal fundraising page or be mailed directly to the LGS Foundation with a note indicating whose fundraiser the donation should be applied to for the purpose of the fundraiser tier prizes. We are unable to count Facebook fundraisers or team totals for this contest. 

*All prizes are exclusive to personal fundraisers who reach these goals…There is no other way to order these items! 

*Deadline to receive donations is May 31, 2023. Prizes will start to be ordered and mailed out after May 8, 2023.

Every dollar raised brings us one step closer to improving treatments and quality of life for those affected by LGS.


All proceeds benefit the LGS Foundation’s  Finding the Cures, Together Program to advance LGS research.

This event is made possible with support from our friends at:

Previous Walks

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

messenger sharing button
email sharing button


Updated 05/17/2023