Cystic Fibrosis Information

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Many people have heard of Cystic Fibrosis, but few know what it is all about.  Gia is typical of many individuals with CF.  She appears to be a happy and healthy toddler.  But beyond this she has a genetic disease that may take her life prematurely.

Cystic Fibrosis is a genetic disorder that affects the digestive system, lungs, and sweat glands.  CFer's have abnormally high amounts of salt in their secretions that causes these abnormalities.  Years ago, children with CF would struggle to survive because of their inability to properly digest food.  This was corrected with the introduction of enzymes.  Since that time the struggle has been centered around the lungs.  A CFer's lungs fill with a thick sticky mucous that makes them susceptible to many illnesses that would not affect non-CFers's.  In recent years the challenge has been against Pneumonia, Pseudomonas Aeruginosa, and Burkholderia Cepecia.

The life expectancy of a CFer has increased dramatically over the past 30 years.  It has increased from less than 18 year to over 32 years.  Now the goal is to increase this much further.  This is why your help is so important.

The Philadelphia Inquirer recently published an article that did an excellent job at educating people about the effects of this terrible disease.  To read Roland Merullo article titled Of Young Life and Breath, which appeared in the April 7, 2002 edition of The Inquirer Magazine, click here.

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This site provides information based on the experiences we have had with Gianna.  Our experiences may differ from others with CF.  Medical information provided is based on these experiences, and information provided by the CF Foundation.  We are not medical care providers.  If medical advice regarding CF is necessary, please seek the advice of a qualified Pulmonologist.   If medical advice regarding cancer is required, please contact your primary care physician or an Oncologist in your area.  We are not responsible for the information provided by sites linked by giannarose.cc, teamgia.com, cfinformation.com, or hepatblastoma.info.  This site is NOT affiliated with the CF Foundation.  Please report inappropriate or incorrect links to webmaster@sitedreamer.com