CF Foundation Responds to Vertex Copay Assistance Program
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The Foundation released a statement strongly urging Vertex to swiftly address its decision to significantly decrease the amount of copay assistance they provide to people with CF, and to ensure no additional burden is placed on the CF community and no person with CF will go without or lose access to essential treatments.
Read the statement »
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Ask the Experts Your Questions at a Live Q&A
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Have a question following this year’s North American Cystic Fibrosis Conference? Get the answers from CF research experts, Raksha Jain, MD, and Jennifer Taylor-Cousar, MD, December 6 at 7 p.m. ET/4 p.m. PT during a live session moderated by James Lawlor, an adult living with cystic fibrosis.
RSVP to the Q&A »
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Vote Now for Your Favorite BreatheCon Design
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Embracing the Realities of Aging With CF
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When Larissa Marocco, an adult with cystic fibrosis, noticed her vision becoming increasingly blurry, she panicked. Larissa’s concerns subsided after she realized she was experiencing normal signs of aging and she reflected on how grateful she is to reach middle age.
Read Larissa's story »
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WE WILL NOT REST UNTIL WE FIND A CURE
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