When my son, Brock, had his first seizure at age 3, we had no idea what was ahead. After months of doctor visits, he was diagnosed with Myoclonic Atonic Epilepsy (Doose Syndrome), and later Lennox-Gastaut Syndrome (LGS). His journey has included the ketogenic diet, a feeding tube for chronic dehydration and failure to thrive, countless medications, and both VNS and RNS implants. It’s been a long road, but he continues to fight every day.

I’m passionate about awareness and education—because too many people don’t understand epilepsy and complex conditions like LGS. Advocacy is not just something I do for Brock; it’s something I believe in for every family walking this path. You don’t have to do this alone. I’m here to listen, share what I’ve learned, and help families feel supported every step of the way.

Languages spoken: English