The Legislative Process and Healthcare Lobbying Hope E. Jenkinson, RN Ohio University The Legislative Process and Healthcare Lobbying The purpose of this paper is to discuss the legislative process and healthcare lobbying. This paper will discuss the political issue of genetic testing. It will explore arguments of both those for the issue and those against it. I will share my opinion on this particular political issue. In addition, this paper will also display a mock letter to Senator Keith Faber, in which I will attempt to sway him to my opinion. Part 1 Legislative Process Anyone can have an idea for a new law, however, they must give this idea, or bill, to their congress representative in order for it to start the process of becoming a law …show more content…
One of these issues is the moral and ethical issue of genetic testing. Genetic testing is a controversial topic that affects patients, fetus to adult. For the sake of keeping this article from being too broad, I will focus on prenatal and fetal genetic testing. Proponents of genetic testing argue that it is a form of preventative medicine, allowing the parents to be prepared or make decisions about a child before the child is born. They may point out that with knowledge of defects or disabilities while child is in utero, medical staff can be ready to act immediately at birth to save the infants life. Place states that genetic testing gives prospective parents a choice in having a child with a disability or birth defect (as cited in Farrelly, et al., 2012). Malik points out that …show more content…
At this time, we do not have the capabilities to alter or remove bad genes from gametes or embryos, but once we do, this will enable us to fix the genetic problem before the child is fully formed and will hopefully decrease the need for termination or birth of children with life threatening disabilities (Malik, 2014). I am concerned with how easily genetic testing could be abused as we cultivate a better understanding of it. In order to prevent this, I believe strict and thorough laws need to be put and kept in place to prevent genetic discrimination and non-therapeutic genetic alterations. I do feel that the pros of genetic testing outweigh the cons by saving lives and should continue. In conclusion the legislative process is lengthy and complex, but this allows for bills to be well deliberated and written before they become laws. It is important that we as nurses are aware of current political issues that could affect us not only as citizens, but in our careers as nurses as well. Genetic testing is just one of the many political issues that affect everyone, including nurses. I feel that genetic testing saves lives but should be closely watched in order to avoid
Guidelines like these need to be formed into a federal law that people can pass in one way or another so that we can be protected from the various forms of discrimination that is possible with this kind of information. The public should be aware of what could happen if this kind of information could become public knowledge, and of the opportunities that the knowledge brings. There is no doubt that the information from genetic analysis is going to help a lot of people with all sorts of problems live longer and healthier lives. The only problem is that we have to keep the information in the hands of those who need it, and out of the hands of those who would use the information to profit or discriminate.
In conclusion, it is important for nurses to have proper training and information in the area of genetics and genomics so that it can be used in daily clinical practice (Thompson & Brooks, 2011). Using this information with clients and conducting a detailed genetic nursing assessment is a valuable component of being an effective health care provider and can help clients recognize, prevent, and/or treat diseases that are unique to their particular
Teutch, S., & Tuckson, R. Department of Health & Human Services, (2008). U.S. system of oversight of genetic testing: A response to the charge of the secretary of health and human services. Retrieved from website: http://osp.od.nih.gov/sites/default/files/SACGHS_oversight_report.pdf
The purpose of this paper is to discuss the Legislative Process and Healthcare Lobbying in the United States of America. Before a law is passed and implemented in America under both state and federal level, it has to go often time through a very lengthy legislative process except in the case of an executive order. And, without the skills and expertise of the lobbying strategies, the idea which might intended to become law may not even make it to the level of a bill not to mention the chance of it to become law. It is important for us as nurses, to understand the legislative process and become very familiar with the lobbying process and take early and prompt action to defend our interests and help prevent any negative impact that any idea or bill that may become law may have on the nursing profession.
People should not have access to genetically altering their children because of people’s views on God and their faith, the ethics involving humans, and the possible dangers in tampering with human genes. Although it is many parent’s dream to have the perfect child, or to create a child just the way they want, parents need to realize the reality in genetic engineering. Sometimes a dream should stay a figment of one’s imagination, so reality can go in without the chance of harming an innocent child’s life.
Genetic testing has been a very controversial topic. While some people believe that genetic testing is completely right in any situation, others believe that it is completely wrong in any situation. However, both sides prove valid points of why genetic testing is both right and wrong. Genetic testing can be very good when it is being used for helpful reasons. However, genetic testing can also be very bad when it is used for the wrong reasons. Genetic testing is okay to do as long as it is being done for the right reasons and following good moral guidelines.
The Human Genome Project is the largest scientific endeavor undertaken since the Manhattan Project, and, as with the Manhattan Project, the completion of the Human Genome Project has brought to surface many moral and ethical issues concerning the use of the knowledge gained from the project. Although genetic tests for certain diseases have been available for 15 years (Ridley, 1999), the completion of the Human Genome Project will certainly lead to an exponential increase in the number of genetic tests available. Therefore, before genetic testing becomes a routine part of a visit to a doctor's office, the two main questions at the heart of the controversy surrounding genetic testing must be addressed: When should genetic testing be used? And who should have access to the results of genetic tests? As I intend to show, genetic tests should only be used for treatable diseases, and individuals should have the freedom to decide who has access to their test results.
In the article “Proposed Treatment to Fix Genetic Diseases Raises Ethical Issues,” written by Rob Stein, the author’s point of view on genetic testing is that although genetic testing can solve one issue, it can generate many other ethical concerns. In other words, Rob Stein mainly shows disapproval to altering DNA, by using pathos, ethos, and logos. He supports his point of view by using mainly pathos to generate concerns. By using questions like “Who am I? Am I a human being like other human beings…?
Kolata, Gina. "Ethics Questions Arise as Genetic Testing of Embryos Increases." The New York Times. The New York Times, 03 Feb. 2014. Web. 18 Mar. 2014.
Morris, D. T. (1993). Cost containment and reproductive autonomy: Prenatal genetic screening and the American health security act of 1993. American Journal of Law & Medicine, 20, 295-316.
In today’s world, people are learning a great deal in the rapidly growing and developing fields of science and technology. Almost each day, an individual can see or hear about new discoveries and advances in these fields of study. One science that is rapidly progressing is genetic testing; a valuable science that promotes prevention efforts for genetically susceptible people and provides new strategies for disease management. Unnaturally, and morally wrong, genetic testing is a controversial science that manipulates human ethics. Although genetic testing has enormous advantages, the uncertainties of genetic testing will depreciate our quality of life, and thereby result in psychological burden, discrimination, and abortion.
There are opposing viewpoints on the incorporation of gene therapy into modern medicine. Many scientists and individuals from the public find genetic therapy to be unethical. In contrast, others see it as a revolutionizing technology that will change medicine and produce treatments and preventions to genetically inherited diseases. Reece briefly mentions the challenging decisions that accompany technological advancements. The ethical concerns that arise with gene therapy include; is the usage of DNA technology adequate to determine if people have genes for inherited diseases, should the tests be voluntary, should genetic testing be obligatory (Reece, et al. 2018). These ethical values vary within people and are commonly determined by values,
Genetic testing, also known as screening, is a rapidly advancing new scientific field that can potentially revolutionize not only the world of medicine, but many aspects of our lives. Genetic screening is the sequencing of human DNA in order to discover genetic differences, anomalies, or mutations that may prove pathological. As genetic screening becomes more advanced and easily accessible, it presents society with difficult questions that must be asked about the boundaries of science and to what degree we are allowed to tamper with the human genome. To better understand the potential impact of genetic screening on our society, we must examine the potential benefits in comparison to the possible negative impact it may cause. With this knowledge in hand, we can examine what the future holds for this field of study and the best possible direction to take.
First of all, I want to start by saying that I 'm not discriminating the disabled community, but this is a very large number that could possibly be diminished with the help of genetic testing. (1) I believe that there is nothing wrong with testing the genes of an unborn child to possibly determine if it could develop a genetic disorder in the future. One of the advantages that genetic testing provides is that the parents could now be informed of the situation, and keep track of their unborn child 's health. I 'm sure those parents are pleased with this technology, and the chances to be able to keep track of their baby. This a baby, and is something very precious, and valuable, and I believe that parents want to keep track of anything that may happen with the unborn child. I 'm sure that a large amount of people would agree would agree that they don 't want to suddenly take the hard hit. When the news is presented in the delivery room. This serves more as an advantage than a disadvantage, due to the fact parents. Pull be more prepared, or possibly have the option to abort it. This is a right that the parents should have regardless of the opposing side arguments towards it. Im a hundred percent sure that the opposing side has very strong arguments towards genetics testing, and one of the main ones is "playing God." The opposing side believed that some things in
Pray, Leslie A., Ph.D. “Embryo Screening and the Ethics of Human Genetic Engineering.” Nature.com. Nature Publishing Group, 2008. Web. The Web.