@sj333love: My son Jesse has epilepsy. It’s not just the seizures—it’s the fear, the unpredictability, the exhaustion. It’s watching your child lose moments of joy, confidence, and freedom. It’s explaining again and again why he can’t join in, why he needs things done differently, why I’m always on edge. People see a smiling boy. They don’t see the aftershocks. The brain fog. The visual overload. The hours of recovery. The toll on both of us. This condition changed our lives—and yet so many still don’t understand how deeply it affects every part of our day. This is more than medical. It’s emotional. It’s isolating. And it’s ongoing. Please don’t look away. Please consider donating to help him get extra treatments… link in bio at bottom of about me page or subscribe to support us linked in post. #EpilepsyAwareness #dayinmylife #tonicclonic #grandmalseizures #focalepilepsy #invisibledisability