There is no cure for cystic fibrosis, and far too many people with CF lose their lives too soon. While medical advancements have improved treatment options, this disease still places immense limitations on those who live with it. Today, approximately 40,000 children and adults in the U.S. have a CF diagnosis—including my son, Christian. He didn’t ask for this condition, yet every day, he shows me just how strong and resilient he truly is.

For many parents, accepting and explaining CF to their child is an incredibly difficult challenge. Simple activities, like sharing Play-Doh with friends, come with risks that most kids never have to think about.

Cystic fibrosis is a genetic, life-shortening disease that affects the lungs, pancreas, and other vital organs. It makes breathing difficult and fighting infections an ongoing battle, often leading to severe lung damage and respiratory failure.

Every person with CF faces their own unique journey, but one thing remains the same—this disease is relentless. While research has led to life-changing treatments, there is still a long way to go. We need a cure so that every person with CF has the chance to live a full, healthy life.

I’m asking for your support in reaching my fundraising goal. Your donation and/ or prayers has the power to push research forward, advance the science, and bring us closer to the dream we all share—a cure for everyone with cystic fibrosis.