LGS Foundation


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LGS Foundation
LGS Foundation


LGS Foundation
LGS Foundation


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LGS Foundation


LGS Foundation
LGS Foundation


Lennox-Gastaut syndrome, or LGS, is a
rare form of childhood-onset epilepsy
which usually appears between the 2nd
and 6th year of life. The syndrome is
characterized by frequent seizures and
multiple seizure types, behavior issues,
mental retardation, regression, and a  
resistance to medications or therapies.

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The LGS Foundation is a
nonprofit organization
dedicated to providing
support and information
about Lennox-Gastaut
syndrome while raising
funds to help pursue
additional research and
services for LGS families.
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Copyright LGS Foundation 2009 | This website was sponsored by Eisai Inc.
Join us for our 2nd annual wine-reception
fundraiser at Martha Clara Vineyards on Long
Island, NY.


The LGS Foundation will be participating in the
2010 "National Walk for Epilepsy". Click here to join
our team!

New genetic study is being conducted to identify
new causes of LGS. Click
here to learn more.

The Epilepsy Phenome/ Genome Project (EPGP) is
looking for participants for an epilepsy research
study. To learn more, go to:
www.epgp.org
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