There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends and co-workers who struggle every day just to breathe.
Southern States Insurance
Walks for Emily
How you can help.
1. MAKE A DONATION through one of our employees from the list below.
2. JOIN OUR TEAM to either walk with us or start your fundraising or both.
By becoming a member of our team and making a donation, you are joining a growing group of people committed to finding a cure for cystic fibrosis. Together, we are adding tomorrows to the lives of people living with CF by supporting the search for a cure. —Southern States Insurance
Frequently Asked Questions
What is 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. A defective gene and its protein product cause the body to produce unusually thick, sticky mucus that clogs the lungs. This leads to life-threatening lung infections, and obstructs the pancreas, preventing natural enzymes from helping the body break down and absorb food.
How does the CF Foundation help?
The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all the people with the disease the opportunity to lead full, productive lives by funding research and drug development, promoting individualized treatment, and ensuring access to high-quality, specialized care.
What is Great Strides Atlanta?
Great Strides Atlanta is a fun, family-friendly event that raises awareness and support for people with CF and their families. The walk will be taking place May 20, 2023, in downtown Suwanee, GA.
IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.