For a child with cystic fibrosis life is mostly a series of respitory infections doctors visits and medications. Cystic fibrosis causes a build up of mucus in th lungs making breathing difficult . The thick mucus coats the hairlike projections lining air passage weakening the bodys immune system .Excess mucus interfers with the functioning of other oragns too.In the liver and pancreas mucus blocks the flow of the digestive enzymes in the intestine so food is not digested properly. Worn down by the repeated bouts of illness a cystic fibrosis patient rarely lives beyond his or her twenties. Cystic fibrosis is most common inherited disorder among Caucasian people. The disease which begins in infancy afflicts more than 25,000 Americans and causes more than 500 deaths every year. Forty years ago the average life span of a cystic fibrosis patient was five years .Today improv....

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