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Not only does this disease block the airways with the thick mucus in the lungs but also blocks passages to major organs including the pancreas, liver and the reproductive system.
In the “1930’s, 80% of infants diagnosed with CF died before their 1st birthday.” (Whitford, 2005). In 1980, the average life expectancy for 82% of CF patients was 12 yrs of age; this was due to the research conducted to improve the treatments available (Cystic Fibrosis Foundation, 2004).
Despite the attempts to find a cure for Cystic Fibrosis (CF) the disease is still killing children and adults every year, the search for a cure is doing more harm than good therefore researchers should not focus funding and research on finding a cure...
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