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I got a postcard from Epilepsy Advocates about a free event they are holding in Dallas. Looking at their calendar, they have these same event across USA.
The event is directed at not just people who have E, but family and friends that want to learn more. I am going to the Dallas event...you might be interested in seeing if there is an event near you
http://www.epilepsyadvocate.com/events/calendar.aspx
They have an E patient tell their story, they have a doctor to discuss new options, as well as answer questions and they provide time to meet other in your area with E. I am excited to go
The event is directed at not just people who have E, but family and friends that want to learn more. I am going to the Dallas event...you might be interested in seeing if there is an event near you
http://www.epilepsyadvocate.com/events/calendar.aspx
They have an E patient tell their story, they have a doctor to discuss new options, as well as answer questions and they provide time to meet other in your area with E. I am excited to go