Reference no: EM133635947

Read the article below and answer the following questions:

1. Summarize your Typical Communications Theory that you've worked on.

2. Did you learned something about the use of communications theory? Was there an "aha" moment?

Cystic Fibrosis (CF)

Cystic fibrosis (CF) is a hereditary disease that is recessive and affects the liver and lungs. Mutations in the CFTR gene cause the condition because CF is autosomal recessive, meaning that you would have inherited two copies of the gene, one from each parent. Two indicators that a person has cystic fibrosis include a persistent cough and an elevated risk of lung infections. The ability of the cilia to get rid of thick, sticky mucus is what causes this. The patient's weight lose also contributes to digestive problems. Other complications may include greasy, bulky stools, difficulty with bowel movements, and infertility in males (HHS, 2023).

This implies that infections may eventually arise from pathogens like bacteria becoming lodged in the lungs. Furthermore, improper cilia function results in the inability to transport mucus, which in turn causes inflammation. This results in symptoms like a chronic cough. This is due to mucus clogging in the digestive tubes, which inflames the pancreas and leaves scars. This occurs as a result of enzymes building up in the pancreas rather than going to the digestive tract. Additionally, the pancreas' natural function is impacted by scarring, which makes the organ slow since it produces less insulin, which is necessary to control blood sugar levels (CFF). What to learn from this disease is that our family genes have a huge impact on our health in the long term. The family genes can affect several generations, not only one. The mutated gene that causes cystic fibrosis (CF) is inherited; an individual with CF had it from both parents. Because there is typically no family history of CF, the birth of a child with CF comes as a complete surprise to the family (HHS, 2023).

Other impacts in other areas in life include lung infections and more severe lung conditions that either don't go or return; pancreatitis is an inflammation of the pancreas that either never goes away or returns; liver illness or cirrhosis, deficits in vitamins, inability to prosper. This indicates that the youngster is not developing and growing as he or she should (Hopkins Medicine, 2021).

 

When left untreated, cystic fibrosis is a systemic disease that significantly affects both the amount and quality of life. Thus, the goal of treatment should be to maximize function in order to prevent acute sickness episodes. This should focus on preserving lung function by vigorously preventing respiratory infections and removing mucus from the airways, maximizing nutritional status by taking multivitamins and pancreatic enzyme supplements and managing any other health issues that may emerge. The best way to do this is to work with experts who have previously managed cystic fibrosis. In those with cystic fibrosis, lung illness is the leading cause of death. Therefore, it is critical to have a low threshold for diagnosis and intervention in cases of exacerbation of pulmonary illness.

A pulmonary exacerbation is an infection-related deterioration of lung function. Fever, exhaustion, intense coughing, and dyspnea are frequently present symptoms of this. Testing for pulmonary function will deteriorate from baseline during an episode. Admission to a hospital with experience managing cystic fibrosis should be the first response to any acute illness.

Abnormal fluid collection in the lungs, pancreas, gut, and other places is part of the typical anatomy for people with cystic fibrosis. Although the exact etiology of this anomaly is unknown, it most likely has something to do with the functioning of the cystic fibrosis gene. This fluid buildup results in tissue damage and inflammation. People who have cystic fibrosis thus frequently experience breathing and digestive problems. Additionally, they run the danger of contracting additional illnesses like pancreatic cancer and liver sickness (Wang, 2020).

CF gene mutation is usually the cause of cystic fibrosis (CF). The proteins that make up CF tubes and sacs are produced by the CF gene. These proteins aid in controlling how much water and salt the body absorbs and excretes. Regular CF testing can help avoid the condition. Antibiotics and air conditioning therapy, which cools the lungs and digestive tract, are the main treatments for cystic fibrosis (CF). Although CF cannot be cured, there are therapies that can help manage symptoms. A fatal genetic illness that affects the digestive and respiratory systems is called cystic fibrosis (CF). In order to prevent CF, people must lead healthy lifestyles.

I agree that the key to early diagnosis and treatment of this illness, which enhances the quality of life for people who have it, is screening. Living in a dry, calm atmosphere is recommended for those who have cystic fibrosis (CF), since this will help prevent the disease from developing.