Welcome to Team Brady’s Bunch! We’re so happy you’re here! Our son, Brady, was diagnosed with Juvenile Myoclonic Epilepsy almost 3 years ago. We were devastated and scared at the onset of his symptoms and diagnosis. I remember feeling like he was an infant all over again as I didn’t want him out of my sight. We are grateful for his doctors and that he lives a normal life with the help of his daily medication. While Brady will likely live a very normal life, we understand that this is likely lifelong for him. We also know that many people suffer from epilepsy. The Hundley Foundation offers hope to those battling this disease. We’re so thankful for this organization and hope you’ll join our team to lace ‘em up and walk with us to help in the fight against epilepsy. Lots of love, The Hoyt Family