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 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.