Advocacy

The Epilepsy Foundation of Delaware has an active grassroots advocacy network where consumers influence changes in all areas which impact people with epilepsy at local, state and national levels. Individual involvement is a powerful tool to effect necessary changes for the best interests of people and families coping with the challenges of epilepsy. We encourage everyone to get involved. The more people our legislators hear from, the greater the chance of bringing about change. Let us know if you are interested in hearing about and responding to legislation of interest to people with epilepsy.

If you want to contact your legislators, please refer to the link in the lower right hand corner of this page.

The Jeanne A. Carpenter Epilepsy Legal Defense Fund has been created to help people with epilepsy fight discrimination - learn more at http://www.epilepsylegal.org.