Persuasive Essay On Genetic Makeup

When I was told that I was going to get my DNA test results back, I felt two distinct emotions during that moment of waiting. Nervousness and excitement followed. True fully, I’ve always thought I knew what I’m susceptible to getting in the future or right now in the present. Due to the fact, I’ve had a talk with both my parents about what family diseases are getting passed along in both my family trees. It’s pretty common diseases: diabetes, hypertension, Parkinson, asthma, hearing loss, and COPD, etc. The few minutes of waiting to get my test results back, made my anxiety levels increase as well as my emotions increasing. When I was given my test results, I immediately ripped open the envelope and read the company’s informational letter. It described to me what PersonaGen Cooperation stands for, Privacy Policy, and how they were capable of finding out certain information about me through viewing my genetic data. I then seemed at my test result paper seeing that I have three different chromosomes that show I’m homozygous or heterozygous for those traits. These results will either show what I need to commute on my health of living style, and what precautions I might need to take in the near future. All I know is that it’s make or break time.

It is patients’ right to opt for genetic testing on their own DNA, although they are accepting a great risk by doing so.

As you can see genetic testing is very important and can affect a child's and parents lives for the better and the worst. Children all over the world have serious genetic diseases that affect their life on a daily. Some of these diseases are Achondroplasia, Down syndrome, and Turner's syndrome. Many believe genetic testing is a good way to test for these genetic conditions before the child is even born, but others think that it can harm the baby very badly and even cause a miscarriage, so they choose not to do this kind of testing. Knowing about the most serious genetic diseases is very important for expecting parents to be informed as well as being

The inclusion of genetic testing into Electronic Health Records impacts the overall healthcare of patient’s because it informs the physicians and other medical professionals the selection of effective treatment or preventive action. A manager’s responsibilities are to implement policies to protect the confidentiality, privacy, and security of genetic tests results and information of patient’s. Policies contributing to potential discrimination acts are also advised because genetic/genomic testing reveals a patient’s physical characteristics.

Due to the lack of adequate interpretation, I do not foresee buying my genome sequencing in the near future. A few of my close relatives have certain medical conditions that concern me, such as diabetes, cardiovascular disease, and rheumatoid arthritis. Even so, I prefer to live a life without the fear of what my DNA profile might uncover. If the test determined that I have an increased risk of developing Alzheimer’s disease, my stress level may increase every time I lose my keys. For example, I have a friend that was terrified of having a child that may have schizophrenia because the child’s grandmother suffered from the condition. During her daughter’s infant years, my friend suffered from stress as she watched for any sign of mental illness in her daughter. My friend suffered from constant worry and guilt that her child would become ill. Her daughter is almost thirty now and she shows no sign of the disease. Even though the test may reveal an increased risk for certain conditions, it is not advanced enough to predict with certainty what my health picture will be in thirty years. I believe in knowing what family risk factors affect me and

According to Berger (2014), a patient can receive genetic counseling to learn more about a condition/disease he or she may possibly be at risk for and may possibly pass onto their children (p. 88). A genetic counselor is educated and trained to describe to the patient the condition/disease, the benefits and drawbacks for taking the genetic test, the test results’ meaning, and how having the condition could affect their future children (Berger, 2014, p. 88). Then, the patient – not the genetic counselor – makes decisions about his or her next steps with respect to all the information they have been provided by the genetic counselor (Berger, 2014, p. 89).

Basically the article claims that everyone is impacted by genetic testing, either positively or negatively. There are many potential benefits which can arise as a result of genetic testing such as individuals that are identified as carrying potentially harmful genetic alterations can receive regular

This is just my opinion on what I would do about the issues relating genetic testing with the American Society of Human Genetics. If you have an immediate family member with a genetic disease or condition, you should have a blood screening test ran to possibly save you from getting the same

I think in an advancing society it is necessary but, with limitations. A person has a right to know about their future children and is entitled to avoid anything they may consider to be too troubling to handle; however, patients should be made aware that the results may be negative or defamatory. But, access to this kind of information requires a serious amount of sensitivity and the person handling it should be aware of this and understand that the only ethics that have entitlement in this situation are the subjects’ . I think it’s all very delicate and subjective. There should be many considerations when having a child or dealing with one’s genetics but, the most important one is quality of life. As long as the ethics support that they are not only beneficial but,

Genetics are the foundation of every human make up, but most people have little to no knowledge of their own foundation. Though some people believe that the encryption of their genetics ruins the surprise in life, other people want to be as prepared as possible for any issues that are encoded in their genetics and cannot be prevented. Genetic counselors test people of any age to uncover a mysterious condition. Counselors can find the likelihood that an adult will develop cancer or will develop a condition that starts in the late stages of life. With the new knowledge, a patient can be better prepared for their future. Counselors can also complete prenatal work by focusing on the parents’ genetics. They test for conditions like down syndrome

According to Harmon (2007), “the public is unprepared for such information and that it is irresponsible to provide it without an expert to help put it in context” (p. 1). Unlike Harmon who actually had her DNA sequenced, I do not plan on obtaining a DNA profile. I understand that if will inform me that I may be prone to some genetic diseases, Alzheimer’s, prostrate cancer, Type 2 diabetes, along with Crohn’s disease. Harmon states “DNA is not definitive” (Harmon, 2007, p. 1).

I agree that a disadvantage to genetic testing may result in discrimination. After learning more about the Genetic Information Nondiscrimination Act of 2008, I find it interesting that the law not only restricts genetic information but also includes one’s individual and family medical history (NIH, 2014). The Genetic Information Nondiscrimination Act took effect in 2009, and also resulted in amendments to the Health Insurance Portability and Accountability Act in 2013, to clarify genetic information as health information (NIH, 2014). Another interesting fact regarding the Genetic Information Nondiscrimination Act is that it does not cover government based health insurers, such as military, veteran, or federal employee health benefits (NIH,

After the completion of the Human Genome project, breakthroughs in associating gene variations to drug response or risk of certain medical conditions provided an avenue for genetic technology. The numerous applications that genetic information could play in a someone’s healthcare also provided an environment where consumers could be perceptive to the idea of obtaining their genetic information. Though advancements were made in genetic information and technology, the average consumer could not afford the testing provided by the traditional testing as part of a healthcare system. So a clear advantage of DTC genetic testing is the reduced cost associated with these companies. Some other advantages in allowing consumers to access their genetic information include consumer empowerment, and making informed decisions about healthcare. Studies have shown that consumers feel more empowered to make informed choices about their health when their genetic risks are known.3 But the limitations still exist with consumer accessing their genetic information, especially when the test reveals negative

I do not have any children and I do not think that I would want my child tested for genetic defects. However,

It comes with many different pros and cons. Actually the cons out way the pros when it comes to this topic. The first pro that comes to mind is that the capacity to acquire individual hereditary data rapidly and secretly without a "remedy". The data can incorporate illness inclination and transporter status. This means that genetics cane me cloned faster and easier then we all think. The second pro that I came up with is the ability to make lifestyle changes, such as diet and exercise, based on the testing results. The third pro is Access to intriguing data about parentage. Many organizations offer testing administrations that will focus the vicinity and rate of ethnic, geographic and even Neanderthal DNA. The last and final pro that I came up with is that the relative moderateness of DTC testing contrasted with different types of hereditary testing. Numerous organizations offer administrations for a couple of hundred