Events for May 22, 2023 – LGS Foundation

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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.
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- 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.
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- 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.
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- 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.
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8:00 pm

May 22, 2023 @ 8:00 pm - 9:00 pm EDT

Caregiver of Adults with LGS – Monthly Support Group

Virtual

Living with LGS is a marathon, not a sprint. Caring for an adult with LGS can be every bit as demanding as caring for a child with LGS, and the need for support is great. Not only do the needs...

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6030 Santo Road, Suite 1, Unit 420878
San Diego, CA 92142
info@lgsfoundation.org
(718) 374-3800

A very special thank you to the TSC Alliance, Dravet Syndrome Foundation, and Child Neurology Foundation for assisting in preparing this website. This website is made possible through grants from our partners. Partners did not have a role in developing content. Thank you to:

Aquestive Eisai Jazz UCB

The information you obtain at this site is not, nor is it intended to be, medical advice. Full Disclaimer
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