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.
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3 min read
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.
1 min read
The 19th annual Volunteer Leadership Conference (VLC), was held in Denver, CO from March 23-25, 2023. It was a special moment to reunite, share stories, and receive updates on the medical progress being made for those living with cystic fibrosis.
1 min read
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.
2 min read
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.
8 min read
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CF Foundation national and local events, provide your company with opportunities to align with a results-driven organization and better position your brand.
1 min read
As a volunteer, you’ll join thousands of people across the country who are helping add tomorrows to the lives of people with cystic fibrosis.