Walking for Cole
IMPORTANT NOTE: To protect the health and well-being of the cystic fibrosis community and CF Foundation staff during the COVID-19 outbreak, the Foundation will not hold any in-person events between March 16 and June 30. Learn more about virtual participation and join us on June 5th.
WINE & DINE FOR CF
PLEASE NOTE: DATE CHANGE
Join us at Founders Hall on Monday Novemver 8th, 2021 for the sixth annual Wine & Dine for CF, featuring a 6 course dinner from some of the top chefs in Charleston and a silent auction.
All proceeds to benefit the Cystic Fibrosis Foundation
Cole’s Journey
Cole was born a Micro Preemie (25w4d @ 1lb 12oz) on January 10th, 2013. Three weeks after Cole was born his newborn screen came back positive for Cystic Fibrosis.
READ COLE’S JOURNEY
What is Cystic Fibrosis?
Cystic fibrosis is a life-threatening, genetic disease that causes persistent lung infections and progressively limits the ability to breathe.
People with Cystic Fibrosis take a combination of treatments including airway clearance, inhaled medicines and pancreatic enzymes on a daily basis. With your help, the CF Foundation is devoting their time and energy to develop new therapies to help people with Cystic Fibrosis live a longer life.
