SUGGESTS A REASONABLE PROCESS OF TREATING THE DISEASE BY ENSURING THAT PROPER METHODS ARE USED IN THE TREATMENT PROCES

SUGGESTS A REASONABLE PROCESS OF TREATING THE DISEASE BY ENSURING THAT PROPER METHODS ARE USED IN THE TREATMENT PROCES

Paper details There are three things that you need to add to the paper: 1) a methods section 2) an intended outcome section 3) needs to be in future tense. Please complete the attached paper according to instructions in the paper details.

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Introduction
Cystic fibrosis (CF) refers to an inherited problem of the mucus glands. Mucus is a substance that is usually secreted by the body to cover the digestive system, lungs, and reproductive system as well as other tissues and organs. CF makes the body release excessive mucus that is extremely thick and sticky, which can cause various health issues. Among these health issues are difficulty in coughing, chest repetitive infections, lengthy diarrhea and deprived gain of weight. If the condition is not treated on time, it can cause extensive complications that may lead to early death. Nevertheless, if the condition is identified early and the child is exposed to proper treatment, the symptoms of CF are controllable and children may live longer. Different authors have different views on CF as they all try to get into a conclusion on how the health condition should be resolved. Since CF is inherited, the defective gene must be passed from both of the parents to the child in order to acquire the disease. In case a faulty gene is inherited, the child becomes a carrier. Actually, carriers of cystic fibrosis do not have the disease, but they can pass it to other individuals. Today, there are many theories on how to improve the treatment process, as well as challenges that can arise when providing medical care.

Literature Review
According to Norm Brown (2009), the gene responsible for CF was identified and it was named Cystic Fibrosis Trans-membrane Conductance Regulator (CFTR). He introduced sweat testing which brought in the non-invasive diagnosis, which was considered as gold standard for CF testing. He suggested proper screening of children after birth to prevent the spread of the disease (Vanzo, 2009). According to the research carried out by NBS (Wilson et al., 2015), CF patients have better pulmonary function in later childhood than the patients diagnosed after clinical symptoms or CF patients who had meconium ileus. The diagnostics can also be carried out with help of the sweat chloride testing (Wilson et al, 2015). Although, Norm believes the disease is genetic (Peebles, 2005), and argues that the disease may develop because of a certain lifestyle, and living in extremely cold and stuffy areas can cause the disease. Scientists also suggest proper screening for children to avoid the conditions of the disease which may not be discovered from genetic identification (Elborn et al., 2000).
In further discussion, Giddings (2009) argues that CF is usually incurable if it is not treated early enough. At some point, the problem may not be noted very fast in a way that the family would call for first response by the doctor. He also argues that the accumulation of mucus in the lungs continues to make the situation even worse. The argument is supported by Orenstein, Spahr and Weiner (2012), who state that the mucus becomes infectious once it starts accumulating in the lungs and other organs. As a result, other complications may develop rendering the organs irresponsive to medication and the necessary treatment (Wolter et al., 2002). As such, the authors suggest that it is better to treat the disease earlier, which calls for families to be on the look to the symptoms of the disease.

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