Cystic Fibrosis Foundation

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Recognized globally, the CF Foundation has led the way in the fight against cystic fibrosis, fueling extraordinary medical and scientific progress. Pursuing a cure for cystic fibrosis and supporting people with CF to live long, fulfilling lives. The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with CF the opportunity to lead long, fulfilling lives by funding research and drug development, partnering with the CF community, and advancing high-quality, specialized care.

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1955

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Address: 4550 Montgomery Avenue, Suite 1100N, BethesdaWeb: Sign in to see organisation websiteFacebook: cysticfibrosisfoundationX (Twitter): CF_FoundationEmployees: 847Volunteers: 53389Revenue: 292016280ICO: 131930701

Home | Cystic Fibrosis Foundation Utility Main navigation Home Welcome to the CF community. Youre in the right place and were glad youre here. We invite you to explore opportunities to get involved and to get support. Cystic fibrosis is a genetic disorder that affects the lungs pancreas and other organs.

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Cystic Fibrosis Foundation

Happy Clinical Trials Day to all cystic fibrosis research teams and study participants who pave the way for new treatments. Today, we celebrate your contributions to clinical trials that have led to incredible breakthroughs in treatments for CF, making life with CF better for everyone in the CF community.

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Brian

Let's support the CF community and help drive research towards a cure! Every effort counts, and I'm proud to stand with you all. 🌟 #CureCF #HopeForTomorrow

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Monica

So inspired by the incredible work the Cystic Fibrosis Foundation is doing! Together, we can make a difference in the lives of those affected by CF. 💪❤️

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Victor

1. What role do community support networks play in improving the quality of life for individuals living with cystic fibrosis?

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Jennifer

2. How can advancements in genetic research and therapy contribute to the future of cystic fibrosis treatment and potentially lead to a cure?

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Cystic Fibrosis Foundation

“Simon isn't short on confidence, and it really is beautiful,” Nic Allen, a father of a child with cystic fibrosis, said. “He doesn't see CF as a limitation, and goes into every challenge believing that anything is possible. ” Simon was diagnosed with CF shortly after he was born 12 years ago.

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