My family found ourselves a part of the Epilepsy community when our son, Bennett, was diagnosed with focal epilepsy just months before his 2nd birthday and has since been diagnosed with focal cortical dysplasia (FCD). The feelings of helplessness, frustration, and confusion that we felt on that day and every day since is shared by the thousands of parents and individuals affected by Epilepsy and seizure disorders worldwide.

Bennett, now five years old, has endured countless scans, lab draws, medications, and weeks-long inpatient stays - far more than most adults have had to experience throughout their entire lives - yet he continues to be our light - gracing others through his infectious laugh, perfect little smile, and undeniable presence.

I share my son’s story because it’s an example of what has filled me and my fellow Board Members with an overwhelming sense of responsibility and desire to advocate for and serve the epilepsy community throughout the state of Georgia. To ensure individuals with seizure disorders have every opportunity that the rest of society is so easily afforded. To support family members and friends who feverishly seek out education, services, and understanding that might assist them in navigating an uncertain future for their loved ones.

I’m honored and humbled to be given the opportunity to serve as the next Chairman of the Board for the Epilepsy Foundation of Georgia. In the coming years I intend to support the tremendous work being done by our Foundation staff as they further develop programming, support resources, policies, and events that will bring our community together and make it abundantly clear that we are 150,000+ strong in support of you!

I aim to be a listening ear and passionate advocate for our community in Georgia and I encourage you to reach me at bcox@epilepsyga.org to let me know how I can be of service to you and your loved ones.
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