One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.