We want to hear from you! The Cystic Fibrosis Foundation welcomes adults with cystic fibrosis and caregivers of people with the disease who are U.S. residents to share how the cost of life with CF affects you or your loved one’s daily life and access to health care services. The research survey takes about 15 minutes to finish.
We appreciate your insights. Your responses will help the Foundation understand how to inform and support the CF community and care teams in addressing financial issues associated with CF.
