The Lennox-Gastaut Syndrome (LGS) Foundation Is A Nonprofit Organization Dedicated To Improving The Lives Of Individuals Impacted By LGS Through Advancing Research, Awareness, Education, And Family Support.
| Website | http://www.lgsfoundation.org |
| Employees | 12 (9 on RocketReach) |
| Founded | 2008 |
| Address | 6030 Santo Rd Suite 1, Unit 420878, San Diego, California 92124, US |
| Phone | +1 718-374-3800 |
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| Industry | Non-profit Organizations |
| Keywords | Epilepsy Foundation, Childhood Epilepsy, Epilepsy Education, Epilepsy Support, Family Support, Epilepsy Awareness, Seizure Disorder, Patient Advocacy, Seizure Treatment, Medical Research, Healthcare Advocacy, Epilepsy Research, Disability Support, Neurological Disorders, Nonprofit Organization, Developmental Delays, Medical Research Funding, Intellectual Disability |
| Competitors | Epilepsy Foundation, The Charlie Foundation, American Epilepsy Society, Citizens United for Research in Epilepsy (CURE), Epilepsy Society, Epilepsy Action, Brain & Behavior Research Foundation (BBRF), Brain Injury Association of America, International League Against Epilepsy, American Academy of Pediatrics +15 more (view full list) |
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Lennox-Gastaut Syndrome (LGS) Foundation Questions
Tracy Dixon-Salazar is the President and Chief Executive Officer of Lennox-Gastaut Syndrome (LGS) Foundation.
9 people are employed at Lennox-Gastaut Syndrome (LGS) Foundation.
Lennox-Gastaut Syndrome (LGS) Foundation is based in San Diego, California.
Top Lennox-Gastaut Syndrome (LGS) Foundation Employees
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