Scientist-Become-A-Geneticist Career

Biology is an important subject, one in which one can learn about living things. I believe biology will allow for me to succeed in college and within my career plans, mainly because I aim to work in the medical field. In order to become an Optometrist, I will need to be both educated on the human body system and familiar with the anatomy of the human

After my sister lost her battle with cancer, I want to have a better of human genome and the genetically transmitted diseases. My passion is to work in the medical field specially the development of potential drug for cancer treatment and others fatal diseases. My sister endured lot of pain and it breaks my heart to see people battling with illnesses and hoping for better health every day.

The medical advances being made feasible by genetic testing are very exciting. It is possible for people with predispositions for genetic defects to know in advance if they will have a healthy child or not. If they find out there is a problem they can choose to terminate the pregnancy or they can prepare in advance for their child's special needs. There is even new technology called Ex Utero genetic testing. This test is performed on eggs fertilized through in vitro fertilization before they are even put in the mother's uterus. Understanding genes in the developing human will help doctors understand the nature of genetic diseases and may lead to countless other medical breakthroughs. Though it is probably a long way off doctors may one day be able to manipulate genes. If this is possible some genetic problems may be cured.

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 benefits of genetic science for society is for employers who want to know if their employers are in excellent working condition and if the worker will cause them more money when obtaining health insurance. If an employer hires someone that that is healthy then the cost of health insurance does not rise and the employee will not have to downgrade their health insurance plan so that they can accommodate the employee that is not healthy. The limitations of genetic science for society are the possibility of genetic testing causing safety issues at work, the development of a genetic low class, the breach of privilege and confidentiality, and the utilization of genetic bias to excuse different methods of discrimination (Krumm, 2002).

Genetic testing has brought about many changes in the way many couples look at conceiving and raising families. Through genetic testing you are able to screen for the increased chance that a fetus may have one of many congenital disorders, or even identify gene changes that are responsible for a disease that has already been diagnosed (Genetic Testing, March 2015). Unfortunately genetic testing is not always exact, in some cases giving parents false negatives or false positive results. Even if the results are accurate, there is the burden of knowledge once you know the results indicate a genetic abnormality such as Down’s syndrome. While caring for a 2 year old male patient with developmental delays and anotia, I learned that genetic testing had been started but never completed on the child. Genetic testing could help to identify genetic disorders that led to the child’s developmental delays and possible future disorders that may develop. The ethical dilemma I will be discussing to the ANA Ethical dilemma of the impact of informed consent of genetic testing on children for adult onset diseases and disorders.

There are two main ways genetic testing places a constraint on a child’s right to an open future. The first of these is that the revelation of a child’s disease status can change his life narrative and the way parents and others treat him, and substantially alter his or her life’s trajectory (Davis _____). Parents may feel guilty or shelter their not-yet-sick

Genetics can help answer questions about our traits and why we look different and advance in different ways from each other in the world. Chapter 1 explains the basics about how genes work, and the portrayal of DNA and RNA. Chapter 2 describes RNA more in detail and it consist of the explanation of the human genome. Specifically, Chapter 3 clarifies how evolution works and how it relates to genetic and medical research. Furthermore, Chapter 4 and 5 explains the knowledge researchers have about genes role in health and diseases, and how society is affected with the advances in medicine and science given approximate credit to these researchers.

Genetic counseling is the job path I want to take when I am older. This profession has a tough price to pay, especially when talking to patients, because sometimes the truth is hard to hear. This challenge is a daily task for genetic counselors, but the job also has great pay, credibility, and work conditions. If I were to go into this field, it will not only be suitable, it will be enjoyable. Becoming a genetic counselor requires a lot of prep in college and tertiary levels of education, but this career is worthy because of the credibility and enjoyment of the field.

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).

These results may also help doctors make recommendations for treatment or monitoring, and give people more information for making decisions about their and their family's health, allowing them to take steps to lower his/her chance of developing a disease. For example, as the result of such a finding, someone could be screened earlier and more frequently for the disease and/or could make changes to health habits like diet and exercise. Such a genetic test result can lower a person's feelings of uncertainty, and this information can also help people to make informed choices about their future, such as whether to have a baby or

<br>4. The rights of knowing someone's own health status and keeping that information private to oneself should be provided to all members of a society. Only the individual should have full access to information about his own genetic constitution and others should be prevented by legal regulations. As we have said above, the results of genetic tests can sometimes be detrimental to the individual. If a person does not want to know the information, its nobody's business nor right to declare it. This includes even not explaining favorable test results without the individual's request.

When providing genetic testing services, the doctor or counselor should follow a set of principles. The doctor is obligated to explain the procedures and their purposes, describe the risks and benefits to be expected, inform of other alternative (possibly advantageous) procedures, disclose the range of decisions the patient may have to make, and answer all questions openly and

genetic testing, everything has changed. She notes that clinicians now have the ability to diagnose, treat, and monitor a patient’s illnesses or disease progression in an entirely different manner. This is a far cry from the old medical model of responding to a disease (or defect) only after it appears, and then prescribing the recommended medication or intervention. These genetic medical advances sound miraculous and promising, but the ability to test, screen and provide early intervention does not come without many major ethical dilemmas.

There are a wide range of jobs in the field of Genetics. Genetics is important because it gives scientists information on the gene’s of the body, heredity, genetic variation, and how each of these things play a part in the function of a living organism. One job in the field of Genetics is a Genetic Counselor. Genetic Counselors work with people who have an inherited risk of acquiring or also carrying certain genetic disorders. They evaluate the family tree to find where the illness stemmed from, who else in the family has had it and the likelihood that they will suffer from it as well. They help patients gain an understanding of the disorder before it occurs so, they will know how to take care of it in the future. Ordering genetic tests in an accurate way to search for illnesses present in a person’s family.