Empower. Protect. Inform.

The Epilepsy Foundation is a vigorous advocate for people with epilepsy. The Foundation has been active in Congress, the executive branch, and the courts, focusing attention on the needs of those with epilepsy. Priorities for the Foundation include: the availability of affordable quality health care, the search for the cure, and the protection of civil rights for people with epilepsy.

Americans with Disabilities Act

Over the past 17 years, the courts have narrowed the definition of disability so much that people with epilepsy, and other conditions who manage their disabilities, are viewed as “too functional” to have a disability.

On June 25, 2008, the House passed the ADA Amendments Act of 2008. The bill aims to ensure people with epilepsy will be protected from discrimination on the basis of a disability. Learn more.

VA Epilepsy Centers of Excellence Act

Experts believe 30-50% of military personnel affected by TBI will develop epilepsy. Perlmutter and Lamborn introduced HR 2818: VA Epilepsy Centers of Excellence Act to prepare the Veterans Administration for the expected influx of new cases. The bill would create six epilepsy "Centers of Excellence" that will lead the way in diagnosis, research, treatment and surgery.

Epilepsy Foundation Board Member Brien Smith, MD spoke forcefully about the impact epilepsy will have on the future lives of countless veterans. Full story.

More resources:

» Read Dr. Smith's complete testimony.
» High Rate of Head Injuries in Iraq Soldiers Portends Potential Wave of Epilepsy. By Brenda Patoine

Improving Health Coverage in 2008
The Epilepsy Foundation and 47 organizations released a statement calling on the 2008 presidential candidates to propose specific solutions that guarantee effective and affordable health & long-term care for all Americans.
» Read more.