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Cystic Fibrosis

Cystic Fibrosis FoundationWhen the Cystic Fibrosis Foundation was established in 1955, children with cystic fibrosis (CF) rarely lived long enough to attend elementary school. Due in large part to the CF Foundation's aggressive investments in innovative research and comprehensive care, many people with the disease can now expect to live into their 30s, 40s and beyond.



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Stories of Caring
 

AngielThe trip to Africa was already planned, and what a trip it would be for 9-year-old Angiel and her mother, Damaris. They would travel a distance of more than 8,000 miles, and it would take almost an entire day to get there. It was going to be the journey of a lifetime. “Most of my family is in Kenya,” said Damaris. “This was going to be Angiel’s first trip. She was going to meet her cousins and aunts and uncles.”





CAF’s mission is advancing research to cure this fatal blood disease. Enhancing the quality of life of patients, educating doctors, trait carriers and the public.


 

 

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