Taking care of your child or loved one with LGS can be difficult for you and your family.
The LGS Foundation is dedicated to assisting families who are living with Lennox-
Gastaut syndrome with information, resources, support, and more. Please feel free to
contact us with any questions or to inquire on how we can help you further.

Below is a list of ways the LGS Foundation provides assistance:

  • Helping families find local and state resources for their loved one with LGS
  • Providing information on disability rights
  • Offering financial assistance to those who wish to attend select epilepsy
    conferences and events
  • Providing further epilepsy-related resources
  • Helping you advocate in your child's school for the right services
  • Connecting families who share similar experiences or location
  • Assisting your family in obtaining outside services and information, including:
       -Medical equipment and helmets
       -Seizure dogs
       -Various Medication discounts
      
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