2008 to 2023: 15 Amazing Years of Progress!
Formed in 2008, the LGS Foundation has since grown into an internationally recognized nonprofit organization that is improving the lives of those impacted by LGS and accelerating research toward the cures.
The LGS Foundation brings together patients, families, healthcare providers, researchers, and other diverse stakeholders to better understand and treat LGS, and one day, prevent, reverse and cure this devastating disease.
“In Everything We Do, We Believe Every Child And Adult Deserves A Chance To Live Life To The Fullest.”
Harnessing the power of the patient family community, the foundation is leading the charge to ensure that research, care, support services, education, and awareness of LGS are at the forefront of all we do and make an impact in the lives of those living with LGS.
It has been an exciting decade and a half of growth and success for our community.
Because of you, we have much to celebrate and amazing things to look forward to in 2023!
LGS FOUNDATION OFFERS TIMELY, IMPACTFUL SUPPORT PROGRAMS FOR
PATIENT FAMILIES NAVIGATING THE LGS JOURNEY
Donate now to help support our mission.