Advocacy

The Epilepsy Foundation of St Louis has an active grassroots advocacy network where consumers effect change in the social service delivery system at the local, state, and national levels. Development of services are provided by individual advocacy and systems advocacy.

For further information on who represents you, please contact the League of Women Voters.

At the Epilepsy Foundation of St Louis, we believe that by raising the level of awareness and teaching the general public about epilepsy, we can help reduce the fear and stigma associated with the disorder. If you are interested in advocating for epilepsy, contact us at (314) 645-6969.

Advocates can speak up at any age!  One advocate is a young boy who went to Washington to lobby his Representatives on issues that affect people with seizure disorders.  You can read his story below.

My Trip to Washington by Colin Bush.