ABOUT the LGS Foundation
The LGS Foundation is a non-profit organization dedicated to providing information about
Lennox-Gastaut Syndrome while raising funds for research, services and support for
individuals living with LGS and their families.

The LGS Foundation is based in New York City and provides services and information to
thousands of members across the world. To learn more about our programs and services,
click here.
LGSF board of directors
LGSF professional advisory board
Christina SanInocencio
President
New York, NY

Melinda Hartsook
Vice-President
Verona, VA

Kristen Schoen
Treasurer
Edgewater, NJ

Wendy Flammia
Miller Place, NY
Advocacy Officer

Tashana Small
Patchogue, NY

Kim SanInocencio
Middle Island, NY
Michael Chez, MD
Director Child Neurology
Sutter Neuroscience Group
Sutter Memorial and General Hospitals
Sacramento, California      

James Wheless, MD
Professor and Chief of Pediatric Neurology
Le Bonheur Chair in Pediatric Neurology
University of Tennessee Health Science Center
Director, Neuroscience Institute & LeBonheur
Comprehensive Epilepsy Program
LeBonheur Children’s Medical Center
Clinical Chief  & Director of Pediatric Neurology
St Jude Children’s Research Hospital

Tracy Dixon-Salazar
, PhD
Postdoctoral Fellow
University of California, San Diego
Howard Hughes Medical Institute
Gleeson Lab
La Jolla, CA

Tracy Glauser, MD
Director, Comprehensive Epilepsy Center
Co-Director, Genetic Pharmacology Service
Professor, UC Department of Pediatrics
CONTACT the LGS Foundation
LGS FOUNDATION:
192 Lexington Avenue
Suite 216
New York, NY 10016

Telephone: +1 718 374-3800

E-mail:
info@lgsfoundation.org
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