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 aim to understand the experiences and needs of individuals in the CF community, including those who may be 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 our efforts, and ultimately enable us to better track our progress in improving outcomes for people with CF. By voluntarily providing your information, you are helping us ensure the CF Community Blog represents all perspectives of the CF community.