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.
New to LGS
- 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.
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Home / Get Connected and Supported / Attend an LGSF Family MeetUp

Attend an LGSF Family MeetUp

LGS MeetUps are peer-facilitated get-togethers for anyone who has lived experience with Lennox-Gastaut Syndrome. Our team endeavors, as a community, to build an empathetic, supportive, non-judgmental environment; one that allows us to share ourselves, voice our experiences and offer peers an opportunity to relinquish emotional weight.

LGS can feel isolating, but you don’t have to walk this journey alone.

The LGS Foundation is pleased to offer a variety of Community MeetUps. Whether you are new to LGS or have been navigating this journey for many years, you can find valuable information and true friendship at our MeetUps.

Want to Connect?

Attend an LGSF Family MeetUp

Join our PRIVATE Online FAMILY Support Group