Describe diagnosis and treatment of Cystic Fibrosis

Describe diagnosis and treatment of Cystic Fibrosis
Cystic Fibrosis Assignment

Cystic fibrosis is the most common autosomal recessive genetic disease of white Indo-Europeans (Caucasians). Three main systems are usually affected by cystic fibrosis. These include the lungs and respiratory tract, the digestive tract (especially the pancreas and intestines) and the sweat glands.Cystic Fibrosis Assignment The lungs will normally have a thick mucus line them in cases of cystic fibrosis which requires physiotherapy to dislodge the mucus and create sputum. The digestive enzymes that would come from the pancreas are blocked by the thick mucus; thus the person afflicted with the disease has trouble digesting foods that are high in fat and protein. In cases that involve cystic fibrosis the salt that is lost during perspiration is much more than in

This activity is especially frustrating in the adolescent years when resistance comes into play. Parents find that the teenage years are the most grueling because there is a rebellious stage that most teenagers go through anyway. Having this disease on top of that is almost asking for further trouble. Cystic Fibrosis Assignment
The well siblings of those who are afflicted with this disease do not see it as a problem. Early on in life they are observant of their parents’ frustrations, but later learn that this is just another facet of life that is dealt to certain individuals. They see that their parents do not treat them any differently than their sibling who has the disease. ” ‘We both have to do chores,’ ‘She does the same amount,’ ‘We get treated the same’ are not uncommon among those families with sick and well children” (Bluebond-Langner 201).

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The life of the child with this debilitating disease is not always as easy as some of these previous books have lead one to believe. This disease affects the person who has it, the siblings in the household, anyone who comes into contact with the sick person, and especially the parents of the sick individual. Yes, the afflicted is the most directly influenced by cystic fibrosis, but it is the parents who must provide most of the care to the person afflicted. This is a disease that is primarily identified

Cystic Fibrosis is a genetic disease that affects many people today. It takes over a person’s whole life to survive this disease. To survive, people who suffer with Cystic Fibrosis need constant care of this disease. Cystic fibrosis is disorder that is inherited and causes severe damage to the lungs and digestive system. Cystic fibrosis changes the cells that make mucus, sweat and digestive juices. These fluids that are secreted are normally thin and slippery. A defective gene causes the secretions to become thick and sticky. The secretions plug up tubes, ducts and airways in the lungs and pancreas. (Cystic fibrosis)Cystic Fibrosis Assignment
In cystic fibrosis, a defect changes a protein in the body. This protein regulates the movement of salt in and out of cells. The result of this change is thick mucus in the respiratory and digestive system. (Cystic fibrosis) The gene mutation is associated with the severity of the condition. Children have to inherit one copy of the gene from each parent in order to have Cystic Fibrosis. If children inherit only one copy, they won ‘t develop cystic fibrosis, but will be carriers and possibly pass the gene to their own children. (Cystic fibrosis)
Cystic fibrosis is a genetic disorder that reduces the life expectancy of the people that are affected. This is common in Caucasians and affects 1 in 3,200 Caucasians. The mutation in the gene varies according to the geographical background. Cystic fibrosis occurs in one out of every 15,000 African-American births. The life expectancy of cystic fibrosis patients has been increasing over the past 40 years. (Pinkerton) Every newborn in the United States is tested for cystic fibrosis. Early diagnosis means treatment can begin immediately Cystic Fibrosis Assignment