What is CF?

Cystic Fibrosis (CF) is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States. A defective gene and its protein product cause the body to produce unusually thick, sticky mucus that:

• clogs the lungs and leads to life-threatening lung infections; and
• obstructs the pancreas and stops natural enzymes from helping the body break down and absorb food.

In the 1950s, few children with CF lived to attend elementary school. Today, advances in research and medical treatments have enhanced and extended life for children and adults into their 30’s, 40’s and beyond.

Our Story

Our son, Brady O’Connell was born March 13^th 2009, and immediately brought us tremendous joy and excitement!  However, our world dramatically changed the following morning when the neonatal doctor recommended transporting Brady to a level 3 Neonatal Intensive Care Unit, and ultimately diagnosed Brady with Cystic Fibrosis.

From day one, the CF Foundation has been an indispensable resource and support system to us, and has made incredible strides in the search for curing Cystic Fibrosis.

SHAMROCKIN 2021 HIKE

Even though our Shamrockin’ for a Cure plans have shifted, we are excited to invite you to be part of a different challenge we are taking on to support the 2021 event! Next spring, our family will be headed to Lake Geneva, Wisconsin to celebrate Shamrockin’ by completing the 26 mile trek around the lake. We invite you to make a donation today!

What Else…

Follow us on Instagram, Facebook and Twitter for the latest news on Brady, Cystic Fibrosis Foundation updates, and more events.  Together, we can all help CF stand for Cure Found!