
Inherent Health Weight Management and Other Genetic Tests Introduction. Find out, based on your genetic makeup, what is the best diet and exercise plan for ‘you’ to efficiently lose weight.

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DTC Genetic Tests – The Good, The Bad and the Future
Doctors, lawyers, pharmaceutical companies, life sciences consulting firms, and health care providers are all keeping a very close eye on the development of government regulations of DTC genetic testing.
As of this post, federal regulations differ from state to state with each having its own full or partial regulations or complete restrictions. Only 12 States allow direct to consumer testing, 13 have complete restrictions in place and 24 have partial limitations to what they will allow. At the present time, both New York and California have complete restrictions against direct to consumer genetic testing, and the companies that want to provide these services are wondering if other states will follow their lead. Many of these companies are locating in the U.S. because of these loose regulations. Countries like the U.K. are not as attractive to this business as strict regulations are already in place.
But many consumers are keeping a close watch on these developments too. There are definitely three factions in the game, those who want it, those who don’t and those who agree that partial restrictions are okay.
Advocates of DTC genetic testing feel that it helps consumers take a proactive approach to their own healthcare. Many believe that testing for diseases such as cardiovascular disease, or cholesterol problems would encourage people to seek professional help sooner than they normally would, and in most cases before symptoms even occur. They are also in support of genealogical testing that can alert individuals to health concerns that may be inherited.
For those against DTC testing, the issues are more moral and ethical. Their concern centers on the many emotional, social and even financial factors that could be overlooked without the guidance of a health care professional. Other moral concerns might be that the day would come, for example, when health insurance companies demand genetic testing before approving policies, or employers demand it before hiring for positions.
Those who support partial regulation can see both the good and the bad. Some of the simpler testing could perhaps be left in the hands of the consumer. The more complicated tests, and those with greater impact on the lives of the consumer, should be administered with both the psychological and medical guidance of the appropriate health care professional.
There are also those who fear that a lack of federal regulation would allow genetic testing companies to take advantage of those somewhat desperate consumers and advertise falsely needed services or charge exorbitant fees.
And then, of course there is the argument that without interpretation of test results by competent professionals, consumers could make poor decisions regarding their present and future health care.
It is, to say the least, a most complex issue, and one that is undergoing very close scrutiny by everyone.
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Every five minutes someone is diagnosed with colon cancer- making it the third most common type of cancer in the US But for some patients, colon cancer may also be a sign of more trouble to come.
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Genetic Testing
Genetic testing is when doctors look at a person’s DNA (genetic information) to see if they or their children are likely to have medical problems in the future. Before doctors could test for genes that might give trouble, they had to understand what genes are and how they work. This knowledge was gained starting in the early 1950s, when the nature of the DNA molecule was first understood. By the late 1980s, devices existed that allow doctors to sequence DNA cheaply and quickly enough to make genetic testing possible. The popularity and usefulness of genetic testing grew during the 1990s. Today it is a common procedure.
Genetic testing can be classified into the following categories:
Carrier identification. Some diseases, called genetic diseases, are passed by their parents to their children. In some cases the parents may not have the disease themselves: a person must have two copies of a defective gene (DNA segment) to get the disease, and often a person has one copy. The person with one copy is called a carrier. If both parents have the defective gene, however, then the chances are high that at least some of their children will get two copies and therefore have the disease.
Prenatal diagnosis. This is when DNA taken from a developing fetus is tested, usually to see if there is mental retardation or some other severe birth defect. Parents sometimes choose abortion if the test shows that their developing fetus is likely to be born with severe mental retardation.
Newborn screening. Newborn screening is when newborn babies are tested to see if they have genetic disorders that can be better treated if treatment starts at once. Newborn screening can test for dozens of disorders, many involving the body’s ability to produce certain substances that are vital to life. If caught early, sickness and death can sometimes be prevented.
Late-onset disorders. Genetic tests are also available for diseases that affect people later in life, such as heart disease, colon cancer, certain kinds of breast cancer, and some other cancers. These tests do not prove that a person is going to have a certain disease, but a positive result means that the person is more likely than other people to get that disease.
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