If you’ve been looking for answers to your health issues with no success, looking at your genes may be the next step. Thanks to new technology, there is now a way to identify variations in your DNA, and for the first time ever – 4W1H Consultancy is now offering this service! Keep reading to learn what genetic testing actually is, who needs it, and why it is important.

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DID YOU KNOW

What Is Genetic Testing?

The purpose of Genetic Testing is to check for any mutations hidden in your genes. Genes Genes are made up of DNA, which is responsible for storing the instructions for all of your body’s functions. Under normal conditions, your genes work properly. But when they don’t, they can cause illness and disease. These mutations can be genetic and can be the main reason you get sick.

How Is DNA Genetic Testing Done? There are numerous ways to test your DNA, both invasive and non-invasive. Tests are performed on samples of fluid (like amniotic fluid or saliva), blood, skin, or even hair. Generally, the most common DNA test kits use a simple cheek swab.

Is DNA Testing Safe? Genetic testing possesses very few physical risks, especially if the test is only a cheek swab. That said, the emotional risks can be a bit greater. Because the information you will get back from a DNA test is in regards to your health, the results could be undesirable.

Keep in mind that the test can only tell you whether you carry the gene mutation for a specific illness. It does not tell you how the illness will progress or whether you will have major symptoms. But this information does allow you to create a prevention plan, or specify how you should be treating the illness.

Why Would You Have A Genetic Test?  Most often, you will want to complete a genetic test if you have been battling an illness or disease for an extended amount of time with no resolution. Genetic testing can help you diagnose the disease, the cause, and can help determine how to treat it.

What does DNA Analysis tell you & the Benefits?

Through Genetic Saliva Testing, your ability to make and use many critical enzymes is measured. These enzymes are responsible for helping keep your cells healthy. The enzymes tested include:

  • Glutathione: Responsible for the detoxification of the body and controlling inflammation
  • SOD: Neutralizes the superoxide free radicals
  • BH4: Supports neurotransmitters and helps the body detox ammonia
  • Neurotransmitters: Aids in emotional health
  • Choline: Enhances liver health
  • Folate: Stimulates cell and neurotransmitter health
  • SAMe: Supports numerous bodily functions
  • B12: Makes blood cells and supports a healthy nervous system

Genetic Testing can be a simple way to change the course of your health. As mentioned, a major BENEFIT is finally having answers to the questions you’ve been asking for, for a long time. The information you get back from this non-invasive and fairly inexpensive test allows you to identify nutritional weaknesses, supplement for your unique needs, and increase the health of your cells thus decreasing the risk of disease. You could be one test away from better health.

Types of Genetic Analysis

Carrier Testing

Carrier Testing is used to identify people who carry one copy of a gene mutation that when present in two copies, causes a genetic disorder.

Predictive & Pre-Symptomatic Testing

Predictive & Pre-Symptomatic types of testing are used to detect gene mutations associated with disorders that appear after birth, often later in life.

Diagnostic Testing

Diagnostic Testing is used to identify or rule out a specific genetic or chromosomal condition. In many cases, genetic testing is used to confirm a diagnosis when a particular condition is suspected based on physical signs and symptoms.

Pre-Implantation Testing

Pre-Implantation Testing also called Pre-Implantation Genetic Diagnosis (PGD), is a specialized technique that can reduce the risk of having a child with a particular genetic or chromosomal disorder.

Pre-Natal Testing

Pre-Natal Testing is used to detect changes
in a fetus’s genes or chromosomes before birth.

Newborn Screening

Newborn Screening is used just after birth to identify genetic disorders that can be treated early in life.

There are many Deseases  related to free radicals and oxidative stress including:

  • ADD/ADHD
  • Alzheimer’s Disease
  • Anxiety & Depression
  • Arthritis
  • Cancer
  • Diabetes
  • Multiple Sclerosis
  • Parkinson’s Disease
  • Fibromyalgia
  • Heart Failure
  • Learning Disorders
TWO TYPE OF GENETIC TESTS

Genetic Tests

Health Gene

Cancer, Cardiovascular, Detoxification Metabolism, Immune Protection

Talent Gene

Personality, Learning Ability, Second Expertise, Health Management