Researchers are exploring treatments that will keep people with cystic fibrosis as healthy as possible until a cure is found. In the first plenary at the NACFC, two CF scientists explain the progress of current research.
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When I decided to study abroad in 1974, I also decided that I would not allow CF to stop me from living my life to the fullest.
This year at the 30th Annual North American Cystic Fibrosis Conference in Orlando we have three sessions just for the online cystic fibrosis community.
In the third plenary, Dr. Wayne Morgan talked about the connection between cystic fibrosis care and the Patient Registry, and introduced a new way for people with CF, along with their families, to help shape the research conducted using the Registry.
If you have cystic fibrosis-related
Check in with your cystic fibrosis care team several months before your trip.
Going on vacation without your child with cystic fibrosis can be hard, but here are some tips to help make it a little easier.
There was a clear message in today's second plenary at NACFC: no matter what role you play -- physician, scientist, person living with CF, parent, fundraiser, regulator -- it is going to take a tremendous team effort to advance new therapies as fast as possible and eventually find a cure for CF.
With the holidays fast approaching, it's time to prepare for the change of schedule in your cystic fibrosis routine.