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Hear from John P. Clancy, M.D., the first plenary speaker at this year's NACFC, about recent advances in personalized medicine, which could allow clinicians to better tailor treatment to the individual with CF. 

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Susan Schept
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Next week kicks off the 29th annual North American Cystic Fibrosis Conference (NACFC), which will feature live-streamed presentations from leaders in cystic fibrosis research and care.

Starting on Wednesday, Oct. 7, you can watch select sessions from NACFC. Highlights include the conference's three plenaries, which will cover personalized medicine; ongoing and upcoming CF clinical trials; and new guidelines for the screening of depression and anxiety in individuals with CF.

Recently, we caught up with the first plenary speaker, John P. Clancy, M.D., to talk about the next steps in personalized medicine, which would allow clinicians to better tailor treatment to the individual with CF. Check out the short video below.

The Foundation will also broadcast a session specifically for people with cystic fibrosis and their families: a "one-on-one” conversation between an adult with CF and Dr. Anna Georgiopoulos. In this session designed specifically for people with CF and their families, the two will discuss the importance of screening for and treating depression and anxiety as part of the standard of CF care.

Register online today. The “Broadcast Schedule” tab houses descriptions of all three plenaries.

In case you can't tune in live, you can watch all streamed sessions following the conference here.

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Topics
North American CF Conference | Researcher Resources | Clinician Resources
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A former journalist, Susan enjoys interviewing researchers and learning about their efforts to find a cure for cystic fibrosis. She writes about the direction of current research and the significance of scientific advances to the CF community. Susan grew up in the Washington, D.C., metropolitan area and lives on the Virginia side of the Potomac River with her husband.

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This site contains general information about cystic fibrosis, as well as personal insight from the CF community. Opinions and experiences shared by members of our community, including but not limited to people with CF and their families, belong solely to the blog post author and do not represent those of the Cystic Fibrosis Foundation, unless explicitly stated. In addition, the site is not intended as a substitute for treatment advice from a medical professional. Consult your doctor before making any changes to your treatment.