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 FOUNDATION IS TO ASSURE THE DEVELOPMENT OF THE MEANS TO CURE AND CONTROL CYSTIC FIBROSIS AND TO IMPROVE THE QUALITY OF LIFE FOR THOSE WITH THE DISEASE

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Address: 100 North Sixth St Ste 604A, MinneapolisWeb: Sign in to see organisation websiteFacebook: cysticfibrosisfoundationX (Twitter): CF_FoundationICO: 136161105

Home | Cystic Fibrosis Foundation Utility Main navigation Home Apply for an Impact Grant. Do you have an idea that could make a difference for the CF community. Whether youre still developing your idea or already running an established program Impact Grants can help you move your vision forward. Cystic fibrosis is a genetic disorder that affects the lungs pancreas and other organs.

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William

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. 💙 #CureCF #CommunitySupport

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William

How can the CF community better support newly diagnosed patients and their families in navigating the challenges of this condition?

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Stella

What innovative ideas have you seen or developed that could significantly improve the quality of life for individuals living with cystic fibrosis?

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Stella

Just learned about the Impact Grants! What a fantastic opportunity for innovative ideas to flourish in the CF community. Let's unite and support each other on this journey! 🌟 #FightCF #TogetherForACure

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Cystic Fibrosis Foundation

May is CF Awareness Month, and it’s also our busiest Great Strides season of the year. With more than 200 walks across the country, we couldn’t do this without you and our incredible Great Strides sponsors, AbbVie, Vertex, and Nestle Health Science. Together, we can make CF stand for Cure Found.

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Cystic Fibrosis Foundation

Upon learning of her newborn son’s cystic fibrosis diagnosis at 2 weeks old, Melissa wanted to find a balance between doing research and protecting her mental health. She shared these challenges with her CF care center social worker, who recommended CF Peer Connect to connect with another first-time mom. After being matched, they’ve discussed the impacts of CF, caring for a newborn, and the joys and lessons of raising a baby.

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Birth Defects, Genetic Diseases Category

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4. Cystic Fibrosis Foundation

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