Cystic Fibrosis Foundation Web Site Rated "Best Of The Web"

Main Category: Cystic Fibrosis
Article Date: 22 Jan 2009 - 2:00 PDT

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The American Thoracic Society (ATS) has rated the Cystic Fibrosis Foundation's Web site-http://www.cff.org- the top online source of information about cystic fibrosis. In its "Best of the Web" review of 2008, the American Thoracic Society evaluated 150 Web sites containing information about cystic fibrosis.

"This is an outstanding site with the most comprehensive and up-to-date information available for most issues regarding cystic fibrosis," noted the American Thoracic Society in its review, adding: "The Cystic Fibrosis Foundation is the preeminent organization involved with matters relating to cystic fibrosis in the United States, if not the world."

The American Thoracic Society conducts an annual review of respiratory health Web sites to help healthcare professionals and patients identify the most reliable, current sources of information. Web sites are rated based on five criteria: authority, currency, accuracy, navigation and readability, and utility. The Foundation's Web site earned the highest rating in all five categories-five stars.

"We strive to provide the best online information about cystic fibrosis and to be a valuable resource for anyone affected by this disease," said Amy DeMaria, senior vice president of communications of the Cystic Fibrosis Foundation. "We are honored to be recognized by the American Thoracic Society."

Read the review here.

About the American Thoracic Society

The American Thoracic Society (ATS) is a non-profit, international, professional and scientific society for respiratory, critical care and sleep medicine. The ATS is committed to the prevention and treatment of respiratory disease through research, education, patient care and advocacy. The long-range goal of the ATS is to decrease morbidity and mortality from respiratory, critical care and sleep disorders and life threatening acute illnesses in people of all ages. In keeping with these goals, the American Thoracic Society interacts with both national and international organizations which have similar goals.

About the Cystic Fibrosis Foundation

The Cystic Fibrosis Foundation is the leading organization in the United States devoted to curing and controlling cystic fibrosis. Headquartered in Bethesda, Md., the Foundation has more than 80 chapters and branch offices throughout the country and supports and accredits a nationwide network of 115 care centers, which provide vital treatments and other CF resources to patients and families.

Cystic Fibrosis Foundation

Article adapted by Medical News Today from original press release.
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MLA
Cystic Fibrosis Foundation. "Cystic Fibrosis Foundation Web Site Rated "Best Of The Web"." Medical News Today. MediLexicon, Intl., 22 Jan. 2009. Web.
14 Feb. 2012. <http://www.medicalnewstoday.com/releases/136255.php>

APA
Cystic Fibrosis Foundation. (2009, January 22). "Cystic Fibrosis Foundation Web Site Rated "Best Of The Web"." Medical News Today. Retrieved from
http://www.medicalnewstoday.com/releases/136255.php.

Please note: If no author information is provided, the source is cited instead.


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