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Positives and negatives of cystic fibrosis
Positives and negatives of cystic fibrosis
Positives and negatives of cystic fibrosis
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Cystic fibrosis, also known as CF, affects over 30,000 children and adults world-wide. CF is a disease in the lungs and digestive system and is still incurable today. It is a disease that causes thick, abnormal mucus in the lungs, nasal polyps, fatigue, and can also damage organs in a person’s body. According to www.cff.org/aboutcf, over 70% of CF patients are diagnosed at two years of age. Cystic fibrosis is one of the most life-threatening diseases in the United States and is very common amongst chronic diseases. Cystic fibrosis is most commonly diagnosed in young children and sometimes adults. I have been dealing with cystic fibrosis my entire life because my fourteen year old brother was diagnosed with it when he was born. He was in the hospital several days after his birth and as a baby, and was in and out of the hospital constantly. He still visits the doctor every few months for checkups and pulmonary exams. In the nineteen-fifties, people with CF didn’t live long enough to attend their first year of schooling. Now in the modern era, patients can live up to their thirties or forties if they’re lucky, but will more than likely lead to death due to lung complications later on down the road. Some of the symptoms of a CF patient are salty-tasting skin, constant coughing, frequent lung infections, wheezing and breathing problems, low immune system and growth, and malfunctions in the digestive system. Some people may go years without showing any symptoms of CF but do have the disease. Most people are diagnosed by two years of age and some may not be diagnosed until later in their lifetime (around the age of 18). Newborns born with cystic fibrosis may not have any signs of a bowel movement within the first 24-48 hours of their li... ... middle of paper ... ...rican Lung Association, 2014. Web. 05 Mar. 2014. "Cystic Fibrosis." Definition. Mayo Clinic Staff, 13 June 2012. Web. 04 Mar. 2014. "Cystic Fibrosis Symptoms, Treatment, Life Expectancy, Genes, Testing - MedicineNet." MedicineNet. Medicine Net, 1996. Web. 05 Mar. 2014. Izenberg, Neil, MD. "KidsHealth Cystic Fibrosis." KidsHealth - the Web's Most Visited Site about Children's Health. The Nemours Foundation, 1995. Web. 02 Mar. 2014 Schoenstadt, Arthur, MD. "Treatment for Cystic Fibrosis." EMedTV: Health Information Brought To Life. Clinearo, Inc., n.d. Web. 05 Mar. 2014. "Sign in." Cystic Fibrosis and Your Baby. March of Dimes Foundation, 2014. Web. 05 Mar. 2014. "Pulmonology." Riley Hopsital for Children. IUHealth, Riley Childrens Hospital, 2014. Web. 5 Mar. 2014. "What Is Cystic Fibrosis?" - NHLBI, NIH. National Institutes of Health, 26 Dec. 2013. Web. 04 Mar. 2014.
Maternal & Child Health Journal, 8(3), 107-110. Retrieved from http://search.ebscohost.com/login.aspx?direct=true&db=a9h&AN=14089739&site=ehost-live.
Cystic Fibrosis (CF) Pathophysiology: Cystic fibrosis is a genetic disease of the secretory glands that affects the respiratory and digestive system. It mainly affects the lungs, pancreas, liver, intestines, sinuses, and reproductive organs. Cystic fibrosis affects the cells that produce sweat, mucus, and digestive fluids. Mucus becomes thick and sticky, causing build-up in the lungs and blocking airways, making it easier for bacteria to develop. This prompts repeated lung infections and can cause severe lung damage after some time.
CF is a chronic condition therefore the patients are either seeking medical attention or receiving (sometime involuntarily) a great deal of medical scrutiny and intervention during their lifetime.
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...
“What is Neonatal Nursing?” Neonatal Nursing Career Info. National Association of Neonatal Nurses, Web. 08 Dec. 2013.
In the Shadow of Illness, the book describes different experiences of families who have or had children with cystic fibrosis (CF). CF is an inherited disease that is passed on from the mother or father who is a carrier, but doesn’t have the condition. Doctors have figured that in this scenario, the parents are likely to have a child with CF. Individuals with CF have to take Cotazymes to help the pancreas digest food. If the person does not take these enzymes, the food goes straight through them as diarrhea. Also, the person’s lungs are affected by a thick mucus that must be removed or thinned before it clogs. Doctors recommend the patient to perform daily breathing exercises that prevent the mucus from thickening; for example, swimming
Cystic fibrosis is one of the most common lethal mutations in humans. The autosomal recessive allele is carried by 1/20 Caucasians, 1/400 couples will have children with the disease, and ¼ children will be afflicted. If untreated, 95% of affected ch ildren will die before age five (Bell, 1996).
In conclusion, Cystic Fibrosis is a very common lifelong condition. This disease causes thickening of the mucus, tears, sweat, and saliva, trouble breathing, and trouble digesting food. If one shows such symptoms, they should immediately contact their doctor or physician. As this disease is potentially life threatening, it is important for people to check to see if they carry or have CF, and begin treatment immediately if they do, in fact, have the disease.
Heart Failure Symptoms WebMD Reviewed by Thomas M. Maddox, MD on May 28, 2012 http://www.webmd.com/heart-disease/heart-failure/heart-failure-symptoms
Cystic Fibrosis is an inherited disease characterized by the buildup of thick, sticky mucous that can cause severe damage to the body’s organs. Mucous is usually a slippery substance that lubricates and protects the linings of the airway, digestive system, reproductive system and other organs and tissue. Problems with digestion can lead to diarrhea, malnutrition, poor growth, and weight-loss. Due to the abnormally thick mucous it can can clog airways, leading to breathing problems and bacterial infections in the lungs. Bacterial infections can lead to coughing, wheezing and inflammation. Overtime these infections can lead to permanent damage in the lungs including the formation of scar tissue, known as fibrosis and cysts in the lungs (Genetics Home Reference, 2013). The symptoms and signs of this disease vary but mostly include progressive damage to the respiratory system and chronic digestive system problems. An individuals’ lungs who are infected by cystic fibrosis have bacteria from an early stage. This bacteria can spread to the small airways, leading to the formation of bacterial micro-environments known as biofilms. Biofilms are difficult for antibodies to penetrate, therefore the bacteria repeatedly damage the lung and gradually remodel the airways, resulting in difficultly to eradicate the infection (Welsh, 1995). Cystic fibrosis patients may even have their airways chronically colonized be filamentous fungi and/or yeasts. Most men with cystic fibrosis have congenital bilateral absence of the vas deferens (CBAVD), a condition in which the tubes that carry sperm are blocked by mucous and do not develop properly. As well, women may experience complications in pregnancy. Either the c...
What Is Polio? What Causes Polio?. (n.d.). Medical News Today. Retrieved October 23, 2013, from http://www.medicalnewstoday.com/articles/
Quinn, P. (2012). Attention Deficit Hyperactivity Disorder: What Is ADHD?. WebMD. Retrieved on December 3, 2013, from
K, Florentyna. "Cirrhosis life expectancy." Living with liver disease. Spruz social websites, 05/21/2010. Web. 4 Nov 2011. .
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.
"Adenosine - What Is Adenosine?" Adenosine - What Is Adenosine? N.p., n.d. Web. 09 Mar. 2014.