Essay On Cystic Fibrosis

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How do you think a person with cystic fibrosis lives? Cystic Fibrosis is a rare genetic disease that affects the digestive and respiratory system. Cystic Fibrosis is more common in caucasians than other race. They have to deal with the symptoms that come with the disease. Someone who is living with cystic fibrosis has many treatments/ therapies.

Cystic Fibrosis is an inherited condition which makes a person develop a sticky mucus that makes it hard to breathe. It affects the lungs, liver, pancreas, and intestines. It affects people of all races and ethnics. Each year 1,000 new cases are diagnosed and about 30,000 are living with cystic fibrosis in the United States. The average lifespan for a person who has cystic fibrosis is 29 years old. Cystic Fibrosis makes breathing difficult and digesting food properly difficult to. In order to get cystic fibrosis both parents have to have cystic fibrosis. Nearly half the population is living with cystic fibrosis that is 18 …show more content…
The most common symptoms are sweaty tasting skin and coughing all the time. Cystic Fibrosis comes with respiratory infections since the disease causes you to produce a sticky mucus substance. Some babies right after birth show symptoms because they become ill. They have respiratory infections and over time they fail to gain any weight that is when the doctors suspect they have cystic fibrosis. Usually around the age 2 is when most people get diagnosed with cystic fibrosis. If you have cystic fibrosis you don’t get all these symptoms right away. The first common symptoms when you first notice you may have cystic fibrosis is when you get respiratory infections. That is when you should get tested for cystic fibrosis. Couples who are thinking about having a baby or already pregnant should get tested for cystic fibrosis. Also if someone has it in your family you should also get
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