Have your gift matched for Giving Tuesday! Dear Friend Ella is a vibrant and active 14-year-old who enjoys dance, soccer, swimming, taking pictures of her cousins and friends, and cooking with her grandmother, Nancy. In between her busy schedule and ke…

Help us go twice as far this Giving Tuesday Dear Friend Join us in celebrating all the progress made this year and planting hope for the years to come. This Giving Tuesday, gifts will be matched, dollar-for-dollar, up to $250,000. The Foundation funds…

Plus Great Strides registration and Path to a Cure Learn How the CF Community is Shaping ResearchJoin us for a free Research Progress webinar on Tuesday, December 10. Hear an overview of the full spectrum of research the CF Foundation is supporting…

Learn more about our progress in infection research Dear Friend, November marks the one-year anniversary of the launch of the Infection Research Initiative. Through this initiative, the Foundation has committed at least $100 million to address the chronic and intractabl…

NACFC starts today Your opportunity to hear about the latest advancements in cystic fibrosis research and care is here! Join us today at 4:30 p.m. CT / 5:30 p.m. ET for Plenary 1 from the North American Cystic Fibrosis Conference (NACFC). …

CF Foundation announces $500 million Path to a Cure Dear Friend, The future of CF has never looked brighter. The CF Foundation’s relentless pursuit of better todays and more tomorrows for people with CF, combined with the efforts of our extraordinary …

Join us Friday to learn more about the announcement Dear Friend, On Monday, we shared the exciting news that the FDA has approved TRIKAFTA™ for people with cystic fibrosis age 12 and older who have at least one copy of the F508del mutation. With the introduction of this…

FDA approves new highly effective treatment for the underlying cause of CF Dear Friends, Today marks a tremendous breakthrough and exciting news for people with cystic fibrosis. The FDA announced its approval of TRIKAFTA, a new, highly effective CFTR modulator therapy …

Learn more about our advocacy work to help CF stand for Cure Found Dear Advocate, Ever wonder how your advocacy helps move the needle on research and development? Join us Wednesday, October 23 at 1:00 PM ET for a webinar to learn more about the F…

Check out the schedule and register today Dear Friend. The North American Cystic Fibrosis Conference (NACFC) brings together researchers and health care professionals from across disciplines to discuss the latest developments in cystic fibrosis res…

Plus the latest research news, getting social without oversharing, and more Navigate Open Enrollment with CompassChoosing the right health insurance plan can be complex, but CF Foundation Compass can help! You can contact a case manager for one-on-…

Plus BreatheCon, the O'Donnell's family story, and more on lung transplant Register for BreatheCon!Come together with other people living with CF to discuss topics unique to you! BreatheCon is a free, online event just for adults with cystic fibros…

Learn tips and tricks to help you make a difference in the community Dear Advocate, School is back in session and our lawmakers are back to work. Join the Cystic Fibrosis Foundation on Wednesday, September 11 at 1:00 PM ET for a webinar to hear m…

Plus 2019 Impact Grants, RNA research, and new fundraising tools Thirty Years, a Lifetime of ProgressThirty years ago this month, scientists discovered the gene for cystic fibrosis. The discovery was heralded as one of the most significant genetic …

Download your Congressional Recess Toolkit today! Dear Advocate, We’re sorry to have missed you at our latest advocacy webinar – but that doesn’t mean you can’t take part in August recess advocacy! Right now, your lawmakers are back in your…

Learn how to help advance policies during Congressional recess Dear Advocate, The cystic fibrosis community has been hard at work advocating both on Capitol Hill and at home for the needs of people with CF. Want to learn how to join this strong, …