Cystic Fibrosis Foundation

September 2017

Clinical Resources

Country of origin: USA

The Cystic Fibrosis Foundation, a non-profit organization devoted to finding a cure for the life-threatening, genetic disease, recently announced the launch of its newly designed website as part of a new overall visual identity.

"Knowing that our website is one of our most important connections to the CF community, we upgraded it to ensure that patients, families and volunteers will find the best and most up-to-date information available about this disease," said Robert J. Beall, PhD, president and CEO of the CF Foundation. "Together we will continue the fight to find better therapies and ultimately a cure."

Features of the new website include:

?Ž Enhanced navigation tools to make searching easier
?Ž Compelling new images of real patients, doctors, researchers and children in the CF community
?Ž New resources for learning about cystic fibrosis
?Ž CF news and announcements
?Ž Expanded information on cystic fibrosis research and clinical trials

In 2007, the CF Foundation plans to add new features and content, including a community section that will have customised information for people who are newly diagnosed, parents, children, teens and adults with CF, as well as for volunteers.

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