A Study on the Hereditary Disease Called Cystic Fibrosis

Cystic Fibrosis is a lifelong, hereditary disease. It usually affects the lungs causing thick, sticky mucus to form, making it difficult to breathe. It also blocks the pancreas pathways leading to the digestive system, which causes problems for properly digesting food. Cystic Fibrosis, also known as CF, is the second most life-threatening disorder, occurring in childhood. Some symptoms of Cystic Fibrosis include, salty-tasting skin, wheezing or shortness of breath, persistent cough, frequent lung infections (such as pneumonia or bronchitis), poor weight gain, and growth.

Typically most people that are Northern European Caucasian descent are more likely to have CF, than any other race in America. Approximately 30,000 Americans have CF, and 1,000s are diagnosed each year. Life expectancy for people who have CF, has gone up since 1930.

Most people back in the 30s, would be lucky to make it to elementary school age. Most people with CF now, have a better chance to live well in their 305 and 405, although some cases are more severe than others.

Being a carrier of the disease may make you reconsider having children, going back to the notion that 1,000 people are diagnosed with this disease each year in America. Imagine if every parent who was a carrier did not have children because they were afraid of being hurt later on in life, that‘s at least 1,000 people who will never be born. We all hope that our children turn out to be healthy babies as they are born. Unfortunately, that isn’t always the case for some families.

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With today‘s technology, parents can get a test to see whether or not they are a potential carrier, not only for CF, but for most diseases as well. Living with Cystic Fibrosis can have a strong psychological impact on the people with the disease and their families and friends.Parents who discover that they are potential carriers of CF, know that their child may only be with them for a short amount of time. Parents may encounter feelings or periods of depression and anxiety, processing emotions such a guilt, worry overtime spent alone or with a partner, or money concerns. The life expectancy for people with CF doesn’t always accurately measure the severity of the disease within each individual person.

Other therapies for CF include airway clearance techniques, such as chest physiotherapy and high-frequency chest wall oscillation, which help to loosen and clear mucus from the lungs, as well as antibiotics to treat and prevent lung infections. Nutritional therapy, including a high-calorie, high-protein diet and pancreatic enzyme supplements, is also important in managing CF. In conclusion, cystic fibrosis is a hereditary disease caused by a mutation in the CFTR gene, which leads to the production of thick, sticky mucus that clogs the airways, pancreas, and other organs. Early diagnosis and treatment are critical in preventing complications and improving outcomes. Research into the genetic basis of CF has led to the development of new therapies aimed at correcting the underlying genetic defect, as well as other supportive therapies aimed at managing symptoms and preventing complications.

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A Study on the Hereditary Disease Called Cystic Fibrosis. (2023, May 15). Retrieved from https://paperap.com/a-study-on-the-hereditary-disease-called-cystic-fibrosis/

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