International LGS Awareness Day & Epilepsy Awareness Month

Help Raise Awareness of LGS this November!

Our Mission: 

To raise awareness for the more than One Million children and adults worldwide living with Lennox-Gastaut Syndrome!

YOU are a part of something BIG, and your efforts make a BIG impact! Please join us in raising awareness for the more than one million children and adults worldwide living with LGS!

Each November, the LGS Foundation organizes international social media campaigns, events, and fundraisers to raise awareness and funds to support the LGS Foundation’s Mission to improve the lives of individuals impacted by LGS through advancing research, awareness, education, and family support..

As awareness spreads, more people choose to stand with us. Together, we get closer to fulfilling the hope of ending the suffering and devastation experienced by those impacted by LGS.

2024 Key Dates: 

How You Can Get Involved:

Check Out Our Awareness Apparel!

Share your Awareness photos all November with the hashtags:

#LGSAwareness  #LennoxGastautSyndrome  #EpilepsyAwarenessMonth 

Give Now to support the LGS Foundation in our mission to improve the lives of those impacted by LGS.


Thank You to Our International LGS Awareness Day Partners


Platinum Level
Silver Level 

Email us at for partner information.

Thanks To YOU, We Raised Over $90,000!

We can’t thank you enough for joining us to celebrate our 15th Anniversary of service to the LGS Community! Because of your generosity, we raised over $90,000 to support, empower, and educate individuals and families impacted by LGS and fund critical research toward the cures.

We could not end the devastation and suffering caused by LGS without you – our amazing community of supporters!



Thank You to Our International LGS Awareness Day Partners

Thank You For Helping Us Raise Over $77,000 For LGS Research & Family Support!

We can’t thank our community enough for joining us at our Every Moment Matters Awareness Dinner this past Saturday. Because of you, we can continue our important work of educating and empowering families living with LGS and funding critical research for cures.


Updated 05/15/2024