As we reflect on 2016, we are so thankful to our friends around the country, dedicated researchers, care center professionals, volunteers and, most of all, those of you living with CF.
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Preston W. Campbell, III, M.D.
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.
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About the CF Foundation
Dr. Preston Campbell served as president and chief executive officer of the Cystic Fibrosis Foundation from 2015 - 2019. A leader at the CF Foundation for more than 20 years, Dr. Campbell previously served as the Foundation's executive vice president for medical affairs, overseeing the Foundation's research, drug discovery, drug development and clinical research programs, and directed clinical research, the Foundation's network of care centers, clinical training programs and the national patient registry database. He initially became interested in cystic fibrosis as a CF camp counselor while earning his medical degree from the University of Virginia Medical School.
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