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 60K for
Research into Lennox-Gastaut Syndrome.
Learn more about Lennox-Gastaut Syndrome here.
About the LGS Foundation's Walk 'n' Wheel
The LGS Foundation is hosting its 6th Annual Walk ‘n’ Wheel 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.
Although great strides have been made, more work needs to be done.
Inspired by those impacted by Lennox-Gastaut Syndrome, our hope with the virtual Walk ‘n’ Wheel is to increase awareness and funding for scientific research to improve the lives of those affected by this devastating disorder.