Cystic Fibrosis: An Overview Essay -- Diseases, Disorders

IntroductionCystic fibrosis is an inherited disease that in the end leads to death. It affects every racial group worldwide, but its prevalence varies from country to country. In those with cystic fibrosis, the lungs and digestive system are primarily affected by the disease. With the new developments in treatment and management, the 50 percent survival prescribe from the 1970s has greatly improved, allowing patients to continue to live their lives longer than ever evaluate in the past. The new developments in prevention of exacerbations, therapy drugs and methods to preserve lung function subscribe done great things to help patients extend their lives. Education is another distinguished aspect of treating cystic fibrosis. For example, to a greater extent the patient knows about the disease and the benefits of the treatment, the more likely he, or she, is to comply with their recommended therapy. Though the treatment can be very costly and time consuming, it gives cystic f ibrosis patients the opportunity to go to school, harbor jobs and even have families. These are normal events that go with aging that umpteen cystic fibrosis patients may never have been able to dream of experiencing.preponderanceCystic fibrosis is a recessive genetic disease. It is seen mainly in the whiteness population, with 1 in 3,000 Caucasians having cystic fibrosis, but does affect every racial group. According to the Cystic Fibrosis Foundation Patient Registry, as of 2008, there were 30,000 patients with cystic fibrosis in the United States. Keeping this in mind, there are almost 1,000 patients newly diagnosed with cystic fibrosis each year. The Cystic Fibrosis Foundation also estimates that there are approximately 70,000 children and adults with cystic fibrosis wo... ...fibrosis. In (2011). A.D.A.M medical encyclopedia A.D.A.M., Inc. Retrieved from http//www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001167/Clarithromycin therapy for patients with cystic fibrosis A randomi zed controlled trial. Pediatr Pulmonol,Galli, F., Battistoni, A., Gambari, R., Pompella, A., Bragonzi, A., Pilolli, F., Iuliano, L., Piroddi, M., Dechecchi, M. C., Cabrini, G.. Oxidative stress and antioxidant therapy in cystic fibrosis, Biochimica et Biophysica Acta (BBA) - molecular Basis of DiseaseDowman, J. K., Watson, D., Loganathan, S., Gunson, B.K., Hodson, J., Mirza, D.F., Clarke, J., Lloyd C., Honeybourne D., Whitehouse, J.L., Nash, E.F., Kelly, D., van Mourik, I., Newsome, P.N.. (2012). Long-term impact of liver transplant on respiratory function and nutritional status in children and adults with cystic fibrosis. American Journal of Transplantation,