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.
Give Now
Search

List View Map View Submit Your Event

This event has passed.

LGS Foundation’s 15th Anniversary Dance Party

August 12, 2023 @ 8:00 pm - 9:00 pm EDT

This family-friendly event is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.

To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Details

Date:: August 12, 2023
Time:: 8:00 pm - 9:00 pm EDT

Organizer

: LGS Foundation
Phone: 718-374-3800
Email: info@lgsfoundation.org
: View Organizer Website

Venue

: Virtual