Welcome to the Georgia Chapter of the Cystic Fibrosis Foundation.
"As the Executive Director of the Georgia Chapter of the Cystic Fibrosis Foundation as well as a parent to a CF adult myself, I want to assure you are not alone in facing CF. I encourage you to connect with our Chapter. I also welcome you to contact me at any time. Even if you are not ready to get involved with the Foundation's fundraising efforts, I am here to provide you with additional information or just listen to your story."
- Scot Rittenbaum
The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all 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.
Patient Assistance Resource Center: We are here for you.
CF is complicated. Getting the coverage you need to stay healthy shouldn't be. The CF Foundation is dedicated to helping all people with CF get the coverage they need to keep their CF treatment on track and stay healthy. We have created a network of resources to help you decide on coverage that's right for you, make the most of your existing health care coverage, or to find programs that can help you pay for treatment.
People with CF, families and care centers may contact the Patient Assistance Resource Center (PARC) at 1-888-315-4154 Monday through Friday from 8:30 a.m. until 5:30 p.m. ET or by email email@example.com. Learn more about PARC and how these resources can help you.