Essay on Cystic Fibrosis A Way of Life - 830 Words

Air the vital ingredient of life. Without air there will be no oxygen. Now imagine having lungs that will not fill correctly. People with cystic fibrosis (CF) live with this everyday of their life. With CF people lack the special enzyme to break up mucous. Without the mucous breaking up the person cannot breathe because the lungs are filled. In life the body cannot function with enough oxygen. Eventually the body starts to break down from the excessive amount of mucous. First the lungs become ineffective and other organs start to fail. The major reason is due to the mucous build up. CF happens because two parents have a defect in the CF transmembrane conductor regulator (CFTR) gene. If a child has only one parent that has a†¦show more content†¦This is due to the lack of the vas deferens, which is the tube that sends the sperms out of the testes to the penis. In woman they can have children they just have more problems with conceiving due to the excessive amounts of mucous in the sexual organs. When the organs fail the only option is a transplant. With lungs there is only a 50% rate of a five year survival rate after a lung transplantation involving the end-stage respiratory disease. With such a drastic survival rate a study was completed to determine if patients could have a better outcome. This study was done to help determine effective methods to enhance lung transplants before surgery; the Doctors placed the recipients on bi-level positive airway pressure ventilation (BIPAP.) â€Å"BIPAP is a noninvasive mode of ventilation administered through a tight-fitting mask to assist spontaneously breathing patients† In the study there were twelve patients that volunteered for the experiment. Out of the twelve; eight of the patients decided not to have the BIPAP on before surgery. The remaining four did allow the BIPAP. In the volunteers to the study that did not do the BIPAP only survived for two months to ten years. While the four, that did the study after two to eight years did not show any bronchiolitis obliterans. Bronchiolitis obliterans is chronic rejection following a lung transplant. The main purpose was to determine if the patients would have better outcomes. The study concludedShow MoreRelatedEssay about Cystic Fibrosis1110 Words   |  5 Pages Life is not measured by the number of breaths we take but by the moments that take our breath away. According to the American Lung association, the average adult takes 15 to 20 breaths a minute resulting in over 20,000 breaths a day. Cystic Fibrosis (CF) is an inherited and obstructive lung disease caused by the overall obstruction of the airways with mucus that form in the lungs, pancreas and sweat glands. 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Preview: Today I will beRead MoreEssay on Cystic Fibrosis Awareness922 Words   |  4 PagesCystic 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 amongstRead MoreCystic Fibrosis : What It Is?1347 Words   |  6 PagesHave you ever heard of cystic fibrosis? If so, do you know what it is? Well, cystic fibrosis is an acquired issue that causes extreme harm to the lungs and digestive framework. Cystic fibrosis influences the cells that deliver bodily fluid, sweat and digestive juices. These discharged liquids are regularly thin and elusive. 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