About LGS
- Like many rare conditions, Lennox-Gastaut Syndrome can be a complete mystery when you first hear about it. Explore this section to get a thorough understanding of LGS—including its causes, symptoms, diagnosis and treatment.
Newly Diagnosed
- A diagnosis of LGS is deeply unsettling and can leave you at a loss as to where to turn for help and guidance. We’re here for you. In this section you will find information, resources, and communities of support for the challenging road ahead.
For Families
- If a loved one is living with LGS, the entire family shares in the difficult journey. How can you keep them safe? Find appropriate medical care? Get the support you need? This section gives answers to these and other critical questions.
About Research
- Even as our understanding of LGS grows, there is so much more to learn. From research grants to conferences, from publications to voice of the patient family, this section provides avenues for furthering your knowledge and impact.
Get Involved
- Host a fundraiser. Volunteer at an event. Shop our LGS store. These are just some of the ways you can lend your personal support to our mission. Check out this section to get started.
Donate
Search

Home / Latest News / LGS Research Roundtable at AES

LGS Research Roundtable at AES

Every year, the LGS Foundation organizes the LGS Research Roundtable at the American Epilepsy Society (AES) annual meeting in an effort to #FreeTheData. Join us as we hear updates from our grant recipients and research collaborations.

2021 Roundtable Agenda

Come hear about the amazing work LGS Foundation has funded! This meeting is set to be a hybrid event with in-person and virtual attendees.

In-Person Registration Now Open

Register to attend in person

Space is limited, so, please register before December 2nd.

Watch Live on December 3rd at 11am CT

CLICK HERE TO WATCH LIVE – COMING SOON

This event will also be recorded. Check back later for the a link to the video.

Thank you to our Supporters