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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
 
In 1993, my parents and I endured a horror that has been visited upon millions of families across the globe – we watched helplessly as my brother Ron died of AIDS. He was only 32. It is hard to believe that over a decade passed, because all I have to do is close my eyes, and there he is – my friendly, outgoing brother who grew up to charm every person who crossed his path, travel all over the world, and embrace the joys of life to the fullest. I wish you could have known my brother.




Supports innovative AIDS research; educates patients, doctors and the public about HIV treatment/prevention; advocates to protect the rights of all people affected by HIV/AIDS.


 

 

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