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    People living with cystic fibrosis face a heightened, life-long risk of infections, and many battle difficult-to-treat infections for which there are no effective antibiotics available. This is not just a problem for people with CF. Each year, 2.8 million Americans acquire serious infections caused by antibiotic resistant bacteria, resulting in 35,000 annual deaths. A robust pipeline of…

    Tweet Tweets with this article
    • “It’s time for Congress to take action to bring desperately needed #antibiotics into the hands of patients who need them most,” @CF_Foundation says. Urge your member of Congress to support the #PASTEURAct. https://t.co/Zn2K79dB7v

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    Testing for CF - 2 year(s) ago

    Diagnosing CF is a multistep process. A complete diagnostic evaluation should include a newborn screening, a sweat chloride test, a genetic or carrier test, and a clinical evaluation at a CF Foundation-accredited care center.

    Tweet Tweets with this article
    • Almost all babies get #NewbornScreening at 1-2 days old. For most, the results come back normal. If a result isn’t normal, it doesn’t mean your baby has the condition. They'll need a diagnostic test, to be sure. See how this works for cystic fibrosis: https://t.co/NFvZMi0zvT https://t.co/DMFdHveXYQ

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    Testing for CF - 2 year(s) ago

    Diagnosing CF is a multistep process. A complete diagnostic evaluation should include a newborn screening, a sweat chloride test, a genetic or carrier test, and a clinical evaluation at a CF Foundation-accredited care center.

    Tweet Tweets with this article
    • Almost all babies get #NewbornScreening at 1-2 days old. For most, the results come back normal. If a result isn’t normal, it doesn’t mean your baby has the condition. They'll need a diagnostic test, to be sure. See how this works for cystic fibrosis: https://t.co/xVBTGJUZbt https://t.co/p3jvROv4XI

  • Mashup Score: 33

    People with cystic fibrosis continue to live longer and healthier lives, and the Patient Registry data support this general trend. To understand what this means for our community, however, it is important to understand how these numbers are calculated and what they represent.

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    • Science is amazing Cystic Fibrosis life expectancy has increased by 44% since the late 90s And this predates the CFTR modulators, which are miracle drugs #PCCM From https://t.co/vpQnc2H01V https://t.co/eyxBfarQtl