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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
 

Mary Carnahan has more reason than most to feel sorry for herself. She suffers from kidney disease and must be hooked up to a dialysis machine three times weekly. She also has emphysema and needs a walker and infinite reserves of patience to get around. So, when a flood last June ravaged the modest Cedar Rapids home she and her husband Carroll shared, no one would have blamed her if she had belly-ached a bit. But that’s just not who she is: “Oh, I was upset that I lost everything in the house – and the house!” says Carnahan, 70, who had been married 45 years.





Funds MS research worldwide, drives change through advocacy, facilitates professional education, and provides programs and services designed to help people with MS and their families.


 

 

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