Go Team Teagan
My name is Erin—though in many circles, I am simply known as "Teagan’s mom."

When Teagan was first diagnosed with Cystic Fibrosis, I was stepping into a world I knew nothing about. Navigating the complex world of a newborn AND treatments,  specialists along with appointments felt overwhelming. However, as our family became more involved in the CF community, I realized just how small this circle is and how important it is to share our story. Events like this are the backbone of our community; they bridge the gap between isolation and awareness, and with awareness comes life-changing support.

Teagan is a vibrant, thriving child today because of the monumental strides in research and medication made over the last several decades. It is important to remember that these medical breakthroughs simply do not happen without the dedication and generosity of people like you.

There is currently no cure for cystic fibrosis and too many people with CF die young. I’m walking to help change that reality.