Cystic Fibrosis Research Paper

Words: 1534
Pages: 7

Deciding to have a child is one of the most important decisions a parent can make. Most people have reason to believe that there is no way their child can have a genetic disorder or have a mutation in their child’s chromosomes to result in a difference in the appearance or functions of their child. Cystic fibrosis is one of the most common recessive genetic diseases passed down to children. The problems it causes, the lifestyle of a patient who has it, and the probability of passing Cystic Fibrosis along to their offspring are all things a person will have to deal if inherited. The disease of Cystic Fibrosis is a genetic disorder which is passed through the egg of a women when a sperm is united with the egg. Women are the only people who …show more content…
One of the ways it is most controlled is through antibiotics and is better controlled. The patients who have cystic fibrosis take a medication called bronchodilator which helps open up airways to breath, relieves the tightness of the chest, and also diminishes the amount of mucus in the lungs (Rosaler, 2007). One negative part of the antibiotics is patient’s bodies develop a drug-resistant bacteria (Robinson, 2003). Several things are done for the patients to help get rid of the thick line of mucus such as a breathing treatment called a flutter in which the patient breaths into and it creates rapid air pressure fluctuations in the person’s airways (Rosaler, 2007). Today, the medical teams who help with patients who have Cystic Fibrosis provide therapy to relieve some of the most severe symptoms (Pelliccia, 2010). With all of the treatments available to help with Cystic Fibrosis, it gives patients a higher survival rate and longer life …show more content…
Ashley was diagnosed when she was three months old because her lung had collapsed. When doctors found that this had happened, they also discovered her digestive system was not working either and her body didn’t have the necessary nutrients. They put her on several medications and had a very intense therapy which consisted of her parents taking a plastic instrument and tapping it on her back in different intervals and in-between her parents doing that she would receive an inhaler to help loosen mucus. A new device was invented where it would vibrate and help her cough up all the mucus in her lungs. She would have to take it to school and use it multiple times throughout the day. Eventually, she was diagnosed with distal intestinal obstruction syndrome which resulted in very high pain levels and she had to stop going to school. During that time she was only 14 years old and the doctors had told her they didn’t know what was to come for her and she did not know how long she would live. Her family relied upon the Lord for strength and understanding. To add to all the pains Ashley was receiving, she was sent a letter from her insurance agency that said when she turned nineteen her insurance would be dropped. If her insurance dropped she would not receive the medicine she needs in order to insure her colon would not bleed