February 22, 2024

Share Your Thoughts About the Cost of CF

How has the cost of living with cystic fibrosis affected your daily life and access to healthcare services? Adults with CF and caregivers of people with CF who are U.S. residents are invited to participate in our research survey and help the Foundation understand how to inform and support the CF community and care teams in addressing financial issues associated with CF. The survey will be available in Spanish in March.

Take the survey today »

Move Your Idea Forward With an Impact Grant

Do you have an idea that could support people with cystic fibrosis or their families? Applications are now open for 2024 Impact Grants, which provide up to $10,000 per year, for up to two years, to individuals or programs that empower people with CF or their loved ones. Whether you’re still developing your idea or running an established program, Impact Grants can help move your vision forward. Submit your application by April 5.

Apply now »

Research Update Webinar Now on YouTube

In case you missed it, the recording from our genetic therapies research webinar is now available on YouTube. Starting from the basics, learn about genetic therapies in CF, including how they differ from existing therapies and the benefits they can potentially provide to any person with CF, including people with nonsense and rare mutations. 

Watch the recording »

Recordings from BreatheCon Now Available

Recordings from BreatheCon — a unique virtual event for adults with cystic fibrosis — are now on YouTube. Watch now to hear our opening keynote with Leah Schwanke and Raeshaun Jones, a session on parenting with CF, and a panel conversation about navigating working full-time with CF.

Get caught up »