A major concern when having a child with an abnormality is the cost. Ironically, many invest a sufficient amount of time in their careers in order to have a well-paying job, however since they put off children until their later thirties or early forties, the risk for abnormalities is higher. When raising a disabled child, Wertz and Fletcher have noted that it is costly and most of the care is done by the mother. Her primary job becomes being a parent. Also, they have to take on the caring mother role for the rest of their life as it is shown many parents are in their eighty’s and taking care of their fifty-year-old children with a disorder. After the parent dies, it then becomes the sibling’s role to take care of the individual. Studies have …show more content…
Wertz and Fletcher have noted that most geneticists will do prenatal testing for anxious women, no matter their age or family history. This is because the women want it; they are not coerced like Lippman believes. Families have said, “the grieving process that began at the child’s birth continues throughout the child’s life” (Wertz and Fletcher 414). Prenatal testing does not remove freedom from a woman, it gives it to the entire family. In the case study entitled “A Mildly Deformative Fetus,” a scenario is presented in which a 42-year-old female’s fetus tests positive for Klinefelter’s Syndrome (XXY) through an amniocentesis. Though Klinefelter’s Syndrome does not result in mental retardation, there is a tendency towards behavioral disorders and infertility. Mr. and Mrs. Brown have different opinions on the scenario; Mr. Brown believes that the child will not be unmanageable and they should continue the pregnancy. Mrs. Brown disagrees and worries about the emotional suffering that could be caused by a sex-identity crisis. She is in favor of an abortion. Lippman would first view the entire procedure as coercive. The idea that she is 42 and, therefore, a high-risk pregnancy should not require her to have
False positive prenatal testing results lead to hundreds of thousands of abortions each year; even when the baby is healthy. Lastly the society often presumes that people with genetic disorders could not get a job and fulfill their lives, however from Waterloo’s 10 year research; it is clear that they could get a job and graduate from high school and fulfill their lives just like everybody else. It is time for the society to stop performing prenatal testing. Further, change and accept people with genetic disorders, because all humans are born
Many people have a negative outlook on prenatal genetic testing but that is because they are not educated on the goals
Due to the loss of muscle mass, protein adequacy is also a problem in older adults because it is not advised to increase protein intake. Limited protein intake may result in vitamin A, C, D, calcium, iron, zinc, and other deficiencies (Grodner, 2012). Overall, Theresa’s small nutrient intake can result in many nutrient deficiencies.
In Improvements in Prenatal Genetic Testing Raise Ethnic Issues, R. J. Crayton produced an article about prenatal testing and whether or not parents should be allowed to have these tests done. First the situation of a high risk baby who will have a disability or defect after birth, so the parents decide to abort the child is being viewed as an inequality to the disabled community. Secondly, certain adoptions are put on hold since the biological parents chose to not carry the unborn child through the entire pregnancy, however, the surrogate mother wants to carry the child through the entire term. Lastly, research shows that the results can be a false positive, so unintentionally the parents decide not to keep the unknown, but healthy baby.
The status of abortion is one that will always be argued amongst the pro-life community and the pro-choice community. Abortion is the deliberate termination of a human pregnancy, most often performed during the first 28 weeks. (Dictionary) Jane and John are two accomplished individuals who put their careers ahead of having children. When Jane became pregnant they discovered that the baby had Down syndrome (Down syndrome is a genetic disorder that causes lifelong mental retardation, developmental delays and other problems. Down syndrome varies in severity, so developmental problems range from moderate to serious.) (Staff) They did not want have a disabled child, so they decide to abort. In this essay I will argue that it is morally wrong for Jane to have an abortion. Firstly I will present the “extreme” conservative argument to support my view, secondly I will consider one objection to my argument and finally I will provide a response to the objection.
Within his paper, Implications of Prenatal a Diagnosis for the Human Right to Life, Leo R. Kass ventures into the reasoning and consequences behind abortion due to genetic defects. The paper begins with the need for justification as to whether abortion is chosen or not. No matter what the decision there will always be an expectation for a given answer, whether a woman chooses abortion or not society will almost as if require reasoning behind the decision. Despite the opinions and differences between people, the expectation of reasoning remains constant. Not only does Kass explain that there is a need for justification, he also provides specific justifications commonly used and defended. Although it has been extensively proven that abortion cannot be justified by claiming that the fetus is merely a part
Prenatal testing is used to help understand the health and state of an unborn child concerning any birth defects or any other health concerns to help families prepare for the child before it is born. Many physicians and families use prenatal testing in order to help determine whether or not a mother will want to continue with a pregnancy if there is “fetal impairment (that) is detected” (1650). This would then allow for the mother to make a selective abortion. While some information is helpful concerning the health state of the unborn child, there needs to be a distinction between acute injury and chronic disability. However, Asch reiterates that the terms “such as ‘heath,’ ‘normality,’ and ‘disability,’ are not clear” terms and that they vary
Gross, S., & McKanna, T. (2015). The evolution of prenatal genetic testing. MLO: Medical Laboratory Observer, 47(5), 14. Retried from
A major challenge to genetic testing is the possible psychological impact a positive result can have for a patient. A patient may feel depression, or anxiety about the result (Garg, & Roth, 2015). It is important to ensure patient understand the meaning of a positive result and the potential
The previous articles show the complexity of the issues surround prenatal screening techniques such as amniocentesis. Such medical procedures can pose potential risks to the mother’s health, and the health of the fetus. Additionally, ethical dilemmas can be raised over the idea of aborting a pregnancy which will likely result in a child with a deformity or abnormality. At the same time, amniocentesis provides parents with the ability to prepare for certain outcomes in the pregnancy, and can also help to avoid the traumatic, and emotional impact parents experience when a child is born with unexpected birth
“I don’t care if it’s a boy or girl. I just want a healthy baby.” Advancements in technology allow parents to learn more than ever about their baby in utero such as the sex, developmental milestones and potentially any congenital defects. A new parents’ greatest fear is that their baby will be sick or struggle to survive; if parents were able to know their child would be born with a condition that would keep them from leading a typical life, should they be able to terminate? Having a disability or congenital birth defect does not mean the same thing for our youth as it did ten, twenty, or even fifty years ago. The same advancements in technology and science that allow us to learn more in utero have enabled us to understand genetic conditions
In some instances, the fetus may die before birth or be extremely underdeveloped. These nonviable pregnancies may require an induced abortion in order to prevent the parent from carrying to term and giving birth to a stillborn child, which is associated with high risks of developing depression and post-traumatic stress (Kelly and Trinidad), or a child who will die within the first days of life. One woman reported that she had an eighty percent chance of miscarriage after it was discovered that her fetus had severe genetic abnormalities, and, if she had carried out her pregnancy, it was likely that the child would not have survived long. She wrote that “we decided to terminate. … Even though I know we made the right choice, I am still filled
I believe that prenatal screening is essential to life. Although a prenatal screening can not diagnose what a baby will have later on in life, it can diagnose what it has now. There is nothing wrong with wanting to know whether or not your baby will be born healthy or not. In our world today, raising a baby with health difficulties is hard. It is a lot of extra patient, time, money, and stress. It's hard for a family to just give up their personal unborn child, but it reality you have to take up challenges you can handle. I don't think it is fair to force a family to have a baby with health difficulties, when they know they are not capable of taking care of he or she. This can lead to the death of a child in a non abortion sense as well as sickness in the caregivers. If a caregiver is not capable of providing care for the child, they are going to be under a lot of mental stress and/or depression which is very unhealthy. I personally agree with the idea that you know yourself better than anyone else. A mother knows what she needs to do when she finds out whether her baby is healthy or whether it is not. I think prenatal screening is useful and should be left up to the mother to decide the outcome of her baby or in other terms express the phrase “it is good(and justified) that you
The periodical Introduced non-invasive prenatal testing (NIPT), this new technique allows diagnosing potential genetic defect at an early stage of fetus's development. The problems with misdiagnosis using NIPT, forces abortion, reduce or terminate research on treatment for genetic diseases arose as the result. The population diverts view on the positive and negative side of
I personally believe that prenatal testing should not be mandatory. Every couple should be entitled to make their own decision whether they want to do it or not. While doctors mean well by performing these test, we need to remember that there is a possibility of receiving abnormal results which can lead to a lot of anxiety on mothers or even worse termination of healthy pregnancies (First Trimester Screen, 2016) .