I’m supporting the LGS Foundation’s mission to improve the lives of individuals and families impacted by Lennox-Gastaut Syndrome (LGS) through advancing research, awareness, education, and family support. Will you join me?

Our son Jackson is 16 years old. It’s hard to believe we’ve been on this journey with seizures for over 15 years. Reflecting on all we’ve been through is both painful and humbling—it’s a reminder of how little control we have and how deeply our faith has been tested.

Jackson’s first year of life was pure joy. I was over the moon to be a mama, soaking up every milestone, every laugh, every little victory. But just after his first birthday, everything changed. Out of the blue, our perfectly healthy one-year-old began having seizures. How could this be? We went through every test, many treatments, and so many medications—but the seizures were relentless.

You know what else is relentless? We are.

And that’s why we’re still here—still raising awareness, still fighting for progress, and still believing that good things are coming. We refuse to give up. We won’t settle for a life defined by daily seizures, sleepless nights, and endless setbacks.

Our story—Jackson’s story—is meant for good. It’s meant to encourage another family to keep going, to find joy even in the hard days, to show up for one more meeting, and to hold onto hope.

Would you please consider helping us raise the funds that are so critical to finding a cure for Lennox-Gastaut Syndrome? Your support truly means the world to us—and to families like ours who continue to fight every single day.

Thank you for being part of our hope.