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. 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 ‘normal’s itu ations.
The upper respiratory tract is normally lined with a little bit of mucus that is sent out of the lung by the constant movement of the cilia that line the respiratory tree. ‘It is clear from detailed research that poor mucus clearance is not due to uneven ciliary beating. However, there is no doubt that mucus is poorly cleared against gravity in the presence of bacterial infection’ (Harris 13-14).
The pancreas itself secretes fluids that aid in the digestion and absorption of food in all of us. When cystic fibrosis is present these enzymes are not going where they are needed. Most of the time there is need for supplemental nutrients, supplemental minerals, and / or dietary management.
The Term Paper on Cystic Fibrosis Child Parents Due
Cystic Fibrosis Cystic fibrosis is an recessive trait on chromosome 7. This disorder affects chloride transport resulting in abnormal mucus production. This lifelong illness usually gets more severe with age and can affect both males and females. Symptoms and severity differ from person to person. Cystic fibrosis is the most common fatal inherited disease among whites and the majorca use of ...
In the case of dietary management there is a plan for seven to eight small meals throughout the day. ‘This meal pattern enables the patient to consume more food without feeling too full and enhances the utilization of nutrients’ (Ek vall 391).
The sweat gland of a cystic fibrosis patient, when viewed under the microscope appears normal. The secretions that the gland gives off are where the abnormality occurs. ‘It is known that the basic defect in cystic fibrosis is expressed as an abnormal regulation of the movements of salt across the layer of cells that line certain specialized ducts such as the sweat gland duct’ (Harris 26).
This causes a great deal of salt loss and therefore requires most cystic fibrosis patients to ingest salt pills to compensate for the loss.
When all of the treatments are used together most patients of this fateful disease live long happy lives. The physiotherapy that they must endure is the most grueling for most of the patients. This involves coughing up as much of the sputum as possible while inhaling a moisturizing mist and getting pounded on the back to loosen the mucus deep within their lungs. 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.
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’ (Blue bond-Langer 201).
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.
The Essay on Is Daycare Beneficial For Children And Parents?
When you are a child, who takes care of you? Now, the cost of living is so high that many people under age twenty-five are moving back in with their parents. Young people are getting married later now than they used to. The average age for a woman to get married is about twenty-four, and for a man twenty-six. Newly married couples often postpone having children while they are establishing careers. ...
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 early in a child’s life and treated from that day forward. As stated before special diets or extra vitamins can be required to help children digest their food properly, and antibiotics are given to fight lung infections. In addition to all of this is the rigorous task of physiotherapy. This must be done two or three times daily so that the mucus does not have a chance to build up and cut off the supply of life giving air. ‘All this treatment is normally given in the child’s own home and has to be provided by the parents.
Obviously such an extensive program challenges even the most able’ (Burton 8).
Emergency hospitalization to combat lung infections and bowel obstructions are other factors that the parents of a cystic fibrosis patient must endure. The child who grows up with cystic fibrosis becomes increasingly aware of his / her differences as he / she gets older. These differences can either inhibit or benefit the child in his / her relationship with others. The friends that he / she makes can help with the daily procedures. This may be hard for them to cope with at first, but in the end will benefit all parties involved.
The friends will better understand what their buddy has to go through with this disease. It will become more acceptable, and fewer people will consider it an inhibition. Rather, it can be viewed as a learning experience for everybody who may come into contact with the child who endures the pain of cystic fibrosis. There are some cases that are not as severe as others are, but there are those that cannot be turned around quite as easily. Whether it is because the treatment did not get started early enough, or the disease is out of control death is a factor that must be considered in most cases involving cystic fibrosis. Death will come to all of one day, but it may come earlier to some.
The Essay on Cystic Fibrosis
... chronic bacterial infections. Lung disease is the main cause of death from cystic fibrosis. Occlusion of ducts in ... to see a large number of children with cystic fibrosis who were dehydrated. At Columbia University, ... cystic fibrosis cases.Since these latest discoveries, CF research has greatly increased. Cystic fibrosis was once considered a fatal childhood disease. Thirty years ago the median life ...
The problems that some families may have with their communication can cause great pain and suffering when it comes time to dealing with the death of a loved one. ‘The long standing problems of communication that exist in many family groups may be accentuated when the prospect of death shows itself’ (Bowers 58).
Cystic fibrosis is a disease that can take the life of some one who is very close to our hearts. Education of the treatments, side effects, and problems involving this disease is key to winning the battle against it.
The more people can know about different situations that better. If there is some one in a school that has this disease try to educate the entire school about this person’s situation so that the entire student body can help in the fight. If educators and students all join in the fight, this disease can be kept down and help those afflicted lead as ‘normal’ a life as possible.
