All college students juggle new responsibilities. For Noah Abesamis, a 21-year-old with cystic fibrosis, those include an extra, invisible burden — hours of daily treatments, countless pills, and the chance of being hospitalized.

Growing up, Noah was hospitalized more than a dozen times, making it hard to make friends, establish routines, and keep up with regular classwork. Despite this, Noah has stayed the course, drawing strength from family and his love of music. Today, he’s a dedicated college student.  

To lead a long, fulfilling life, Noah needs progress in CF. Progress that’s possible with your support today.

Our greatest hope for a cure lies in genetic therapies, which have the potential to benefit everyone with cystic fibrosis. This includes people like Noah, whose rare mutations mean he can’t benefit from current CFTR modulators. Developing genetic therapies is more complex — and costly — than anything we’ve pursued before.

There are only days left for you to make a difference in 2025.

Give now and help fuel our mission, generating scientific breakthroughs that make a real difference for people with CF, like Noah.

www.cff.org

4550 Montgomery Avenue, Suite 1100N | Bethesda, MD 20814 US

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