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.
The stress of genetic testing results, that may shorten your life or have no cure, will disrupt an individual physically and emotionally. Healthy people who carry the burden of having a life-threatening disease lack strong social support and coping skills. “The anxiety of living with the likelihood of one or more specific, chronic, debilitating disease create psychological burdens that outweigh the therapeutic potential of lifestyle changes or earlier treatment due to increased vigilance” (Kjono). Survivors guilt, or a mental condition experienced by those who have survived a catastrophic event that took the life of others’. For example, a brother or a sister who carry a gene alteration, like cancer, and one sibling has an increased potential for diagnosis, the other sibling will feel guilty for escaping the increased risk. Not only can a negative genetic testing result affect your well-being, but also your ability to obtain health and life insurance. “Genetic testing may permit a much more complete and refined classification of people into risk categories, and so move us further away from sharing the financial burdens of illness and further in the direction of individualized premiums based an individual risk factors ("Genetics And The Moral Mission Of Health Insurance"). Only people who will not need health insurance will be able to afford it. It is more reasonable to undergo regular medical check-ups, and screenings to enable early detection, rather than living with the facts."Understanding the value of genetic tests, and when [and] where to use them in the health care system”, is vital to the well-being of those tested.
Prenatally diagnosed fetuses who have defective genes foreshadows a dangerous path towards eugenics.
“In 1972, a year before the Supreme Court’s Roe v. Wade decision legalized abortion on demand nationwide, virtually all children with trisomy 21, or Down syndrome, were born. Less than a decade later, with the widespread availability of pre-natal genetic testing, as many as 90 percent of women whose babies were prenatally diagnosed with the genetic condition chose to abort the child” (Starr).
Every disabled individual has the right to life live along with normal members in society. Aborting a baby who has...