Why are we asking for the following information? The Cystic Fibrosis Foundation believes every person with CF deserves access to early diagnosis, high-quality care, and community support. To foster progress toward this goal, we need to understand the experiences and needs of individuals in the CF community, including those who are underrepresented in our programs. Responsible collection and use of demographic data will help ensure our work is informed by broad and diverse perspectives, allow us to improve and tailor our efforts, and ultimately enable us to track our progress in improving outcomes for people with CF. By voluntarily providing your information, you are helping us identify ways to best serve the CF community.