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Epilepsy Foundation of Connecticut, Inc.
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The Epilepsy Foundation of Connecticut will ensure that people with seizures are able to participate in all life experiences; and will prevent, control and cure epilepsy through services, education, advocacy, and research. With profound shock and sadness we report the sudden death of Susan S. Spencer M.D. (1948-2009) From: The New Haven Register Sunday, May 24, 2009  Download Obituary 2009
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Our Mission:
The Epilepsy Foundation of Connecticut is pleased to announce a new fundraiser in affiliation with our national office called “Talk About It! @ Dinner.” This new initiative debuted with a short video on 
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H.O.P.E.
Helping Other People with Epilepsy Finding an interesting speaker for your meeting is not always easy. Finding an interesting speaker with fascinating and useful information to impart - and who charges no fee - can be even more difficult. I have a topic that I believe you and your members with both enjoy and from which you will all benefit. The topic, of course is epilepsy, a complex and fascinating medical condition. Although epilepsy may appear to touch few people’s lives, consider this. We all know someone with a seizure disorder. We simply may not be aware of it. Few people are also aware that one in ten of us would know how to recognize most seizures. The Epilepsy Foundation of Connecticut’s speaking program is part of a nation project o increase awareness of epilepsy and remove the mystery that surrounds it. All speakers in the program are affected by the disorder, either directly or indirectly. And, each is specially trained and certified in giving presentations to groups such as schools, Lions and Exchange clubs, Jaycees, and so much more. Audiences usually come away from these presentations extremely pleased and enriched by what they have heard. Feel free to email or call Patrick J. Danis, Program Coordinator for the Epilepsy Foundation of Connecticut, to get more information and to schedule your program today. 800.899.3745 |