Delayed puberty is common among young men with CF, but working with your CF care team to ensure you get good nutrition can help encourage healthy development and growth.
We have about 70 chapters and offices across the country that work diligently to raise funds and support our community in the search for a cure. They host events (including virtually and outdoors) and serve as a hub for the CF community. Get to know them!
CF MiniCon: Transplant is a virtual event for people with cystic fibrosis, their family members, and caregivers to learn about advanced lung disease and explore all stages of the transplant process.
Learning that your baby has cystic fibrosis may come as a shock, especially if you do not have a family history of the disease, but you are not alone.
The Ultimate Golf Experience is the Cystic Fibrosis Foundation's premier golfing event. Each year, guests and friends of the Foundation come together for golf, live entertainment, and luxurious accommodations at one of America's most pristine golf resorts, all in the name of adding tomorrows for those with cystic fibrosis.
The 38th Annual Celebrity Ski Weekend benefiting the Cystic Fibrosis Foundation is scheduled for March 2nd – 5th, 2023, in beautiful Beaver Creek, Colorado.
Our corporate champions are an important part of our progress -- with corporate supporters by our side, we continue to advance our goal -- to make CF stand for Cure Found.
Five Feet Apart, a movie about two teens with cystic fibrosis, was released in the U.S. in March 2019. The CF Foundation was not involved in the production of the film. However, we are hopeful that the movie will provide a positive opportunity to increase awareness of CF and the challenges people with CF face living with their disease.