Events from May 24, 2022 – August 17, 2022 – Page 12 – LGS Foundation

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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September 2026
Caregiver of Adults with LGS – September Support Group Meeting

September 28 @ 8:00 pm - 9:00 pm EDT

Virtual

Join us for our monthly Caregiver of Adults with LGS support group. Caring for an adult with Lennox-Gastaut Syndrome comes with unique challenges as needs evolve over time. This group offers a supportive space to share experiences, ask questions, and connect with...
October 2026
LGS New Family Orientation

October 5 @ 7:00 pm - 8:30 pm EDT

Virtual

Welcome. This virtual orientation is designed for caregivers who are new to Lennox-Gastaut Syndrome (LGS) and/or new to the LGS Foundation. During this session, we will introduce you to our mission, walk through key resources and programs, and share ways...