Cystic Fibrosis Essay

Eventually if the cystic fibrosis gets worse, a lung transplant will be a necessity. This disease is not deadly unless not treated in time. In this report, there will be a discussion of several topics described throughout the paper to name a few topics: Background on Cystic Fibrosis, causes, symptoms, treatments and prevention. Background Dr. Dorothy Anderson was born in Asheville, North Carolina on May 15, 1901. She was the only child to both of her parents Mr. and Mrs. Anderson. At a young age she was orphaned, she got herself through school and college with no help. She got her M.D. from John Hopkins School of Medicine in 1926. She discovered cystic fibrosis with her discovery came the examination of a child who had been said died
One of the most life threatening effects of the disease is the lungs. Depending on how vigorous the stage of the disease is individuals with the genetic disease can live with bacteria in their lungs, and infection of the lungs is the major cause of death for cystic fibrosis patients. The thickness of the mucus stops the flow of movement to release from the lungs, and raises the chance of irritation and inflammation in the lungs. The inflammation then swells the passageways, gradually closing them, and therefore, preventing the movement of mucus. Patients will cough repeatedly and forcefully in an effort to clean the mucus out of their lungs. The way a body reacts to infection is by producing more mucus; while white blood cells try to fight the infection which thickens the mucus as the cells break down and release contents. When mucus gathers, it can block the small passageway in the lungs, destroying the chance of a properly functioning lung. The process of being able to breath and get enough air through the lungs can be extremely complicated; causing a person to be always tired, short of breath, and small minded of exercise is common. If respiratory infections repeat it somehow leads to clubbing, the enlargement of the toes and