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How Does Genetic Testing Affect Our Life

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Would you change your life after finding out you are at risk for something. I believe that genetic testing is not needed because it can ruin relationships, cause bias from employers and insurancers, and lastly, it can impact the way that you live your life. Sometimes it can be needed information, but it can greatly change your everyday life. First, knowing your genetic code can ruin relationships. This can be seen when twin siblings Samantha Schilit and Arielle Schilit Nitenson had trouble after Schilit got genetic testing. Schilit found out that there might be troubles for her unborn daughter. Nitenson wanted the doctor to know, but they both knew that their privacy could be invaded. Another example of this could be when Angelina Jolie …show more content…

Dr. Leonard, chair of pathology and laboratory medicine at the University of Vermont College of Medicine and UVM Medical Center in Burlington, Vt., stated that “one concern people have is ‘learning about something they just don’t want to know about.’” Also, there has been a 2% error margin that has led to uncomfortable situations. Lastly, if parents know their child is at a large risk for a disease, could they restrict them? If a child has an increased chance for skin cancer, will the parents never let them go to the beach? These are some questions that can affect the decision to get your genetic code. On the other hand, genetic testing can be a lifesaving aid for those with a severe ailment. For example, say that your family has a risk for colon cancer. If you get testing, you will know if you are at risk. If so, you will know your treatment paths that you could take. Doctors like Dr. Leonard state that they would like to have every person get genetic testing so that ailments like cancer could be caught before they even begin. In conclusion, genetic testing is not needed because of the many consequences. Maybe it soon will be needed, but in the end, that could cause more problems for individuals than solving

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I agree. In some cases, knowing that you have a mutation and will be affected with the disease could be very emotional for an individual. One never knows how they will respond to the result and pretesting counseling may not fully prepare the individual for the result. One question that has been raised is should genetic counseling be allowed for diseases that are not treatable? It is thought that if an individual knows they will develop a condition that has no treatment it could cause psychological harm, stigmatization, and possible discrimination.

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Through DNA testing we can now see which diseases we will likely pass down to our children. Although this ability can be life-saving in the aspect it can be used to prevent diseases in children, it also can affect the parents’ desires

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In the article, “Tighter Access To ‘Death Master File’ Has Researchers Worried,” Brian Naylor addresses how identity theft by obtaining personal documentation may lead to fraud. The Social Security Administration (SSA) possesses a record of over 50 million names of deceased Americans which is known as the “Death Master File” (Naylor 2). Families and services relating to a person’s death inform the SSA about the deceased’s “... Social Security number, name and dates of birth and death” (Naylor 3). Once the SSA receives the person’s data, the organization ensures “...checks don 't go out to the deceased, while survivors get the benefits they are entitled to” (Naylor 3).

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In chapter seven of Genetic Turning Points by James Peterson, the topic of genetic counselors is discussed in terms of their role in the genetic testing process. In my ethical opinion, genetic counselors are a necessary component of the genetic testing process. Without them, ethical lines are more likely to be crossed as I believe more patients would undergo genetic testing without fully understanding what he/ she is giving their consent for and also receive unrequested results. Additionally, I believe that the absence of genetic counselors leads to patients being pressured into receiving tests he/she did not want or ask to take. , and receive unrequested results as well.

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1250 Words | 5 Pages

In "Building Baby from the Genes Up" by Ronald M. Green, Green expresses his view that genetically modifying humans is not necessarily a good thing for human, but that it’s not such a bad thing or inevitable. Green claims that genetic modification is beneficial to society and would help improve living. Green exclaims that genetic modification is an inevitable future and that the quality of the human population will improve. Green proposes the idea that genetic modification will improve the quality of the human population by using it with health related issues such as obesity and dyslexia and that no children will have to suffer anymore because of those problems. Knowing about our gene will give us more freedom according to Green.

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425 Words | 2 Pages

Joan had genetic testing that revealed a risk of heredity breast/ovarian cancer. Joan and her sister are estranged and Joan does not want to disclose the results to her sister. Joan’s sister carries a high risk of developing breast/ovarian cancer (Lea, 2008). Healthcare workers are faced with the dilemma to notify her sister of the results or to protect Joan’s privacy. Ethically the results should be reported to her sister due to it could reduce her risk of developing cancer or can ensure early detection.

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474 Words | 2 Pages

Genetic testing for a predisposition to a disease can be a simple process and can be beneficial to the prevention of life-threatening diseases. It has been done for a very long time with different strategies throughout its existence, including testing a small sample of DNA. It can also relate to literature like Brave New World. Genetic testing for a predisposition to a genetic disease is a way to find out the genetic information of a person including if they have a disease passed down genetically or not. Testing is done by looking at the family history and seeing if there is a disease that is passed down from generation to generation like diabetes and many forms of cancer.

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For instance, in the event in which law enforcement needs to investigate criminal acts to prove someone innocent or guilty. For example Maryland vs King which states that when a police officer arrest someone because they have a suspect of a serious offence , they make need a cheek swab to rove that the suspect is innocent or guilty because of DNA left at the crime scene. Another positive outcome is that your doctors will be able to detect genetic diseases or cancer and treat it before it becomes a problem or takes effect. Although there are many positive outcomes there is a law that does protect you genome. The Genetic Information and Nondiscrimination Act or GINA protects the genetic privacy of the public.

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How Genetics Affect Me Arlet Gutierrez My genetics have affected me in many important ways. Showing a family pedigree, dominant vs recessive genes and non-heritable traits. A family pedigree is when you pretty much show all your family background or your ancestry from the start of everyone.

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Introduction Dr. Gress’s view that the results of a genetic test should be withheld from patients if they are positive is paternalistic, immoral, and does not consider the autonomy of the individual. He holds the position that notifying patients of their genetic status is too harmful and that it is a doctor’s duty to withhold information that could be devastating; however, in doing so, he violates many ethical principles that doctors should exercise. This paper will give an overview on the topic of genetic testing and the ethical and moral problems associated with it, an analysis rejecting Dr. Gress’s view, and a response to an objection to the thesis of which this paper is based on. Presentation of Topic

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Prenatal genetic testing has been a source of controversy over the past few years, and is increasing as medical technology develops. The arguments supporting prenatal testing verses advocates that are pro life no matter what, is under great pressure to decide if prenatal tests are ethical. Bonnie Steinbock, a professor of Health Policy and Philosophy at the University of Albany, and Hank Greely, head of Stanford’s center for Law and Biosciences, both argue against prenatal genetic testing. They both believe that prenatal testing can promote abortion. Although they both share the same viewpoint on how individuals should not use prenatal testing, Greely writes a more persuading and convincing argument due to fewer fallacies.

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Genetic illnesses have always been around without any way to prevent them. With genetic engineering, scientists would be able to remove things such as heart diseases, chances of alcoholism,

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Gattaca shows many times that genetic testing can be beneficial and has completely taken over society but at the same time provides many hardships like discrimination against certain ranks of

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There has been much controversy over whether traditional genetic tests, which are done through healthcare providers or DTC kits are better, and personally, I am against at home genetic testing.

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Some argue that it is against Christianity. Nonetheless, holy books does not have an explicitly written text about genetic screening. The arguments are only constructed from implications of the holy texts. As the holy texts might hold many different meanings, who can know for sure, if genetic screening is just or unjust way? As this topic is very complicated dilemma and needs a further debates to come to a common consensus, one should consider two outcomes: when it is morally accepted and when it is condemned as unethical thing to do.

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