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The 2nd Annual Kickin Kawasaki 5K in Dumas, Texas brought together nearly 250 participants for an unforgettable morning dedicated to raising Kawasaki Disease awareness, supporting families, and building a stronger community. Hosted by the Kawasaki Kids Foundation, this annual fun run continues to grow each year, bringing together Kawasaki Disease survivors, families, community members, sponsors, and volunteers who all share one common goal: ensuring that no child or family faces Kawasaki...

There’s a moment most parents know well. Your child feels warm. Maybe a little off. You check their temperature, give them medicine, and tell yourself it’s probably nothing. Because most of the time… it is. But for families who have faced Kawasaki Disease, that “normal” moment is where everything begins. When Normal Starts to Shift It’s not usually dramatic at first. A fever that doesn’t go away.Eyes that look a little red. A rash that seems random. Nothing screams emergency. And that’s...

At Kawasaki Kids Foundation , we talk often about education, awareness, and family support . But behind every statistic is a child. Behind every diagnosis is a family whose world changes in an instant. Today we share the story of a brave little warrior named Finn. His journey is one that reminds us why early detection matters and why parents should always trust their instincts. Finn’s Story Early October 2023 our son had been dealing with a slight cold. We eventually went to the pediatrician...