Cystic Fibrosis is a lifelong disease that has a harsh negative affect on many vital organs, some of which include the lungs, pancreas, and intestines. This disease causes the mucus, tears, and sweat of the patient to be considerably thick. However, the thickness of such mucus is determined by the severity of the patient’s Cystic Fibrosis. This mucus affects the breathing of those diagnosed with cystic fibrosis, and many have reported an additional trouble with digesting food. One is most likely to have Cystic Fibrosis if their families have a history of such a disease. Therefore, Cystic Fibrosis is a genetic disease that is recessively passed down to proceeding generations. Additionally, this disease most commonly affects those who are Caucasian or of European descent.
Those who have relatives diagnosed with Cystic Fibrosis are at an automatic increased risk to have the disease. For example, in order for a child to have cystic fibrosis, their parents must be carriers of the CF gene. “One CF gene fr...
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...gous to the gene, there is a twenty-five percent chance that the chid will be health, a twenty-five percent chance that the child will have the disease, and a fifty percent chance that the child will carry CF.
In conclusion, Cystic Fibrosis is a very common lifelong condition. This disease causes thickening of the mucus, tears, sweat, and saliva, trouble breathing, and trouble digesting food. If one shows such symptoms, they should immediately contact their doctor or physician. As this disease is potentially life threatening, it is important for people to check to see if they carry or have CF, and begin treatment immediately if they do, in fact, have the disease.
"Cystic Fibrosis Federation Australia Quick Facts." Cystic Fibrosis Federation Australia Quick Facts. N.p., n.d. Web. 23 Jan. 2014.
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