Bill of Rights for People Living with Epilepsy—Partner Organization

Epilepsy Foundation
8301 Professional Place
Landover, MD 20785
www.epilepsyfoundation.org
1-800-EFA-1000

The Epilepsy Foundation is the national voluntary organization that works through information, research, advocacy and service for people affected by seizures.

The Foundation offers assistance to people with epilepsy and their families through the Answer Place, which can be reached toll free at 1-800-EFA-1000 or on the Internet at www.epilepsyfoundation.org. Questions may also be sent to: Epilepsy Foundation, 8301 Professional Place, Landover, MD 20785. Services are also offered through local affiliated Epilepsy Foundations nationwide. Find your Local Affiliate.

Contributors

The Bill of Rights for People Living with Epilepsy was created and developed by Novartis Pharmaceuticals Corporation and the Epilepsy Foundation of Greater New York along with a number of leaders in the epilepsy community including epileptologists, neurologists, nurse practitioners, social workers and most importantly, people living with epilepsy. The Epilepsy Foundation affiliates of Greater Chicago, Los Angeles and South Florida also contributed extensively to the development of the document.

Epilepsy Foundation of South Florida
7300 N. Kendall Drive, Suite 700
Miami, FL 33156-7840
www.epilepsyfoundation.org/southflorida
(305) 670-4949

Epilepsy Foundation of Los Angeles
5777 West Century Blvd., Suite 820
Los Angeles, CA 90045
www.epilepsy-socalif.org
(310) 670-2870 or (800) 564-0445

Epilepsy Foundation of Greater Chicago
17 N. State St., Suite 1300
Chicago, IL 60602
www.epilepsychicago.org
(312) 939-8622 or (800) 273-6027