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Cystic fibrosis report
Research paper for cystic fibrosis
Cystic fibrosis report
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Cystic fibrosis is a genetic disease; it is passed down through families. Cystic Fibrosis causes sticky mucus to build up in lungs, digestive track, and other areas of the body. The mucus clogs can lead to life threatening mucus infections. {Board, A.D.A.M. Editorial. Cystic fibrosis. U.S. National Library of Medicine, 16 May 2012. Web. 11 Jan. 2014.} Some of the most common symptoms of Cystic Fibrosis are salty skin, wheezing or shortness of breath, and persistent cough, sometimes with thick mucus called phlegm. {Phlegm. Dictionary .com. Dictionary.com, n.d. Web. 13 Jan. 2014.} Other symptoms are poor growth or weight gain even with a good diet. {Children's Health." Symptoms of Cystic fibrosis. N.p., n.d. Web. 13 Jan. 2014.} Current treatments of Cystic fibrosis include chest physical therapy; where they pound chest and back allover with device to loosen mucus from lungs, or wear and inflatable therapy vest that uses airwaves to force mucus upper airways. Exercise, and Antibiosis, both oral and IV tube are also used as treatment. {"How Is Cystic fibrosis Treated?" - NHLBI, NIH. N....
Sequeiros, IM, Jarad, NA. 2009. Home intravenous antibiotic treatment for acute pulmonary exacerbations in cystic fibrosis-Is it good for the patient?. Annals of Thoracic Medicine 4(3), pp. 111-114.
Chronic obstructive pulmonary disease or COPD is a group of progressive lung diseases that block airflow and make it hard to breathe. Emphysema and chronic bronchitis are the most common types of COPD (Ignatavicius & Workman, 2016, p 557). Primary symptoms include coughing, mucus, chest pain, shortness of breath, and wheezing (Ignatavicius & Workman, 2016, p.557). COPD develops slowly and worsens over time if not treated during early stages. The disease has no cure, but medication and disease management can slow its progress and make one feel better (NIH, 2013)
Along with the problems of chronic illnesses themselves, many other problems may come. Treatments and medications are just the beginning of things when it comes to problems with illnesses. With cystic fibrosis, you start out with a high number of medications and treatments to begin with. The older you get and the worse your condition gets, the more you take. (“Psychological impact,” n.d.) Many struggles come along with taking these medications and treatments. When children are first diagnosed with cystic fibrosis, they are typically very young. From the beginning, there are many medications and treatments that needed to be taken and done. Sometimes, trying to get children to take medications and treatments is like pulling teeth. The medications for cystic fibrosis are extremely important. If cystic fibrosis patients miss medica...
It affects mainly the lungs and digestive tract. Cystic Fibrosis causes a buildup of thick mucus in the lungs, which leads to breathing troubles. Mucus in the lungs also benefits bacteria that are responsible for infections. A child with Cystic Fibrosis
Web. The Web. The Web. 1 Apr 2011. http://www.medicalnewstoday.com/articles/150999.php>.
The clinical manifestation one may see in patients with chronic bronchitis are chronic cough, weight loss, excessive sputum, and dyspnea. Chronic cough is from the body trying to expel the excessive mucus build up to return breathing back to normal. Dyspnea is from the thickening of the bronchial walls causing constriction, thereby altering the breathing pattern. This causes the body to use other surrounding muscles to help with breathing which can be exhausting. These patients ca...
Pulmonary Fibrosis is a condition where the lung tissue becomes thick and scarred. The thickening and scarring of the lungs makes it hard for the oxygen supply to be delivered throughout the body. The scarring can be caused by many different factors, but it is hard for doctors to figure out exactly what caused the onset of this disease. The damage caused by this disease cannot be repaired. Pulmonary Fibrosis usually affects the age group of forty to seventy years old. Men are more likely to develop this disease, but women can also get this disease. Pulmonary Fibrosis is not a transmittable disease. Little is actually known about how the disease develops. There seems to be a genetic connection and environmental factors that cause the disease to develop.
It is estimated that one in every 3,600 children born in Canada has cystic fibrosis.
U.S. National Library of Medicine, 26 Sept. 2011. Web. The Web. The Web. 19 Nov. 2013.
Cystic Fibrosis is an inherited genetic disorder which makes it hard to breathe because of the mucus build up blocking the airways of someone's lungs . This mucus can also cause more health problems and it would be truly unbearable to live with Cystic Fibrosis . It's a life threatening disorder that can only be treated . Cystic Fibrosis can also be referred to with many with many other names such as Mucoviscidosis , CF , and Pancreas fibrocystic disease . This disease is caused by the CFTR gene failing . This makes a protein which causes really sticky mucus that makes it hard to breathe because the mucus gets into your lungs . The gene also causes your sweat to be very salty. There are some prenatal tests for CF such as Chorionic villus sampling
JAMA: Journal of the American Medical Association. 14 Nov. 2001: 2322. Academic Search Complete. Web.
Cystic fibrosis is a life-threatening disease that causes damage to the lungs and digestive system. This disease is constantly being researched to find a cure and to develop different treatments to lessen the disease’s effects. CF causes a multitude of defects to how a person’s body functions because of the gene mutation they are born with.
WHO, W. H. (2008). Tradtional Medicine. available at http://www.who.int/mediacentre/factsheets/fs134/en/ retrieved on 9-11-11 at 10:30 pm.
Ed. David Zieve. U.S. National Library of Medicine, 26 Feb. 2014. Web. The Web.
"MedlinePlus - Health Information from the National Library of Medicine." National Library of Medicine - National Institutes of Health. Web. 06 Mar. 2011.