Every August or September, I take part in the HydroWalk—an event that’s become so close to my heart. I was first introduced to hydrocephalus during a newborn session, and not long after, I learned of another friend’s child living with the same diagnosis.
This walk has turned into a beautiful tradition for me. It’s more than just an event—it’s a way to raise awareness, support families, and help fund the search for a cure. I’m so honored to walk alongside those affected and be part of a community filled with hope, strength, and purpose.
