The Joey O Bocce Classic was founded by Joe O’Connell, his friends and family back in 2008. Despite being a relatively new organization, its impact has already been felt. Close to $100,000 has been raise since its inception. Though strides have been made in Cystic Fibrosis research, we must continue the fight, and researchers believe that one day there will be a cure.

Joe and Kristy, 2009

Joe O’Connell lost his fight with Cystic Fibrosis in November 2009, at the age of 32. He had spent three months fighting in the ICU at Duke University Hospital. During this time his wife, Kristy, gave birth to their daughter, Piper Rose.

Those that knew Joe remember his positive spirit, infectious laugh and zest for life. He was quite the character, life of the party, and friend to everyone. We are inspired by his energy, and continue the march forward in the battle against Cystic Fibrosis.

Cystic Fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide). A defective gene and its protein product cause the body to produce unusually thick, sticky mucus. In the 1950s, few children with Cystic Fibrosis lived to attend elementary school. Today, advances in research and medical treatments have further enhanced and extended life for children and adults with CF.