| 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. . |
| 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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Raising Awareness. Creating Support.
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ABOUT LENNOX-GASTAUT SYNDROME
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Copyright LGS Foundation 2009 | This website was sponsored by Eisai Inc.
Latest Epilepsy News
Individuals with LGS often
require the constant care of a
family member or caregiver.
require the constant care of a
family member or caregiver.
Learn what to expect with
Lennox-Gastaut
syndrome.
Lennox-Gastaut
syndrome.
The Epilepsy Foundation of America
launched a new survey specifically for LGS
parents and caregivers. To participate in
this survey, click here.
The Epilepsy Phenome/ Genome Project
(EPGP) is looking for participants for an
epilepsy research study. To learn more, go
to: www.epgp.org
launched a new survey specifically for LGS
parents and caregivers. To participate in
this survey, click here.
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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