EMFs, retroviruses, chronic diseases and cancer

Cutting-edge science is making new discoveries about a class of pathogens called retroviruses. Dr. Judy Mikovits, Frank Rosetti and other researchers have discovered that human endogenous retroviruses (HERVs) have been evolving in human DNA for probably millions of years. Human endogenous retroviruses represent up to 15% of the human genome itself, from birth and long before, transmitted through our lineages. Another class of retroviruses, called exogenous retroviruses, are pathogens to which we are exposed throughout our lives, often also integrating into our DNA by unique processes.

In healthy cells, however, retroviruses lie dormant. It's only when the body is exposed to unhealthy conditions that the retroviruses "wake up" and cause symptoms. In many people, these symptoms can become chronic and are often debilitating. Experts who have studied this subject believe that the modern epidemic of a variety of chronic diseases with no known causes, also known as "mystery diseases", is ultimately caused by the activation of endogenous retroviruses that live in our DNA.

What does it take to "wake up" these retroviruses? Anything that causes stress to the body and depresses the immune system: nutritional stress and nutrient deficiencies, stressful life circumstances, injuries, surgery, environmental pollution, vaccines, pesticides and herbicides (especially glyphosate) in our food, water and environment, heavy metals, parasitic infections, being sick with a viral or bacterial disease for a long time (or frequently), exposure to things we're allergic to and electromagnetic pollution.

Retroviruses can be detected in our environment (HIV is a common virus), and they then make their way into our cells using an enzyme called reverse transcriptase to synthesize DNA on an RNA template. Retroviruses possess only RNA, and this enzymatic process is necessary for them to replicate in the host cell.

The link between EMFs and chronic diseases, and even some retroviruses themselves, has been established. Incoherent electromagnetic frequencies, especially when we're constantly exposed to various sources, are unrecognizable to the body and make it believe it's under attack from a real, physical pathogen like a virus. So the immune system speeds up in an attempt to combat this invisible invader. However, as there is no viral material, it fights perpetually until the entire immune system is exhausted. Now it doesn't have the energy to fight the real invaders - including the hidden pathogens that lie dormant in our cells, the retroviruses.

Carcinogenic retroviruses

"Retroviral insertion can convert a proto-oncogene, an integral part of cell division control, into an oncogene, the agent responsible for transforming a healthy cell into a cancerous one."

Viral cancers were first discovered in 1911, when American pathologist Peyton Rous isolated a virus capable of causing malignant sarcomas (connective tissue cancers) in chickens, which he named Rous Sarcoma Virus (RSV). At the time, he had been unable to find viruses in other cancers, and so temporarily abandoned his work. Decades later, the importance of his work finally received the attention it deserved and, more than 55 years after his first experiment, Rous was awarded the Nobel Prize in Physiology or Medicine for discovering tumor-inducing viruses.

In 1970, virologists from Japan and America, working independently, discovered an enzyme that could synthesize proviral DNA from the RNA genome of Rous sarcoma virus. The enzyme was called RNA-directed DNA polymerase, commonly known as reverse transcriptase. With the discovery of this enzyme and its actions also came the discovery of the unique class of viruses that have come to be called retroviruses, which use reverse transcriptase as the key to their particularly tenacious and chronic infectious activity.

Then, in the 1980s, HTLV retroviruses were discovered and found to cause leukemia, previously thought to be the result of bacterial infection. Then the HIV (human immunodeficiency virus) retrovirus was isolated and found to cause AIDS.

Electromagnetic fields and virus-induced cancers

"Integration of retrovirus DNA into cell chromosomes results in cancer, but proto-oncogenes do not become cancer-causing genes unless triggered by some other event. Cancers caused by chemical or physical carcinogens in the environment are probably often, if not invariably, due to alterations in the sequences of proto-oncogenes that converted them into oncogenes."

In 1997, a study concluded that exposure to a 50 Hz electromagnetic field (a very low frequency compared with today's electronic devices) induced activation of the Epstein-Barr virus genome in latently infected human lymphoid cells. This is an example of a dormant virus that is activated by electromagnetic fields and only begins to replicate following EMF exposure. Almost everyone's exposure to EMF on a daily basis is much higher today than when this study was carried out. It is well established that the Epstein-Barr virus can cause certain types of cancer (such as stomach cancer), and more recent studies are beginning to link the virus to even more common cancers, such as breast and colon cancer.

Dr. Dietrich Klinghardt is a physician and founder of the Klinghardt Academy, the American Academy of Neural Therapy, medical director of the Institute of Neurobiology, senior clinician at the Sophia Health Institute, and founder and president of the Institute of Neurobiology. He is also an expert on retroviruses and their effects on human health.

Dr. Klinghardt states:

"But over the past two years, we've come to realize that it's still not the depth of the bucket. What's at the bottom of the bucket is a group of viruses. We call them human endogenous retroviruses. These are viruses that are integrated into our DNA. We come with them. But they're silenced. They're silenced largely by two mechanisms. One is called methylation. And the other is called acetylation.

And these mechanisms are destroyed by exposure to Wi-Fi or cumulative exposure to electromagnetic fields. And so, what happens is that these viruses replicate themselves within us."

He goes on to explain how retroviral infections occur with a host of other pathogens on the side that are often more visible: Lyme bacteria, parasites, candida, herpes, mold mycotoxins. These other pathogens cause immune stress and help trigger dormant retroviruses, which then develop into a full-blown infection. So often, when a person is diagnosed with Lyme disease or presents with symptoms of chronic fatigue, candida overgrowth, mold disease or parasitic infection, the root source of the symptoms is the replication and destructive effects of retroviruses that are now activated.

In Dr. Klinghardt's medical practice, they have succeeded in bringing retroviruses back from dormancy by modulating the patient's environment - mainly by controlling EMF exposure and reducing toxic elements in the air, food and water. Then, by taming the retroviruses, other problems such as Lyme, candida, herpes and myriad others begin to resolve themselves by tackling the deeper problem.

He also touches on mental illness, pointing out that the leading diagnosis in the US today is chronic anxiety, and that while toxins such as glyphosate are certainly a considerable factor in this, the main driver of chronic anxiety are harmful EMFs.

Studies have already been carried out

Financially speaking, the telecommunications industry is six times larger than the entire pharmaceutical industry combined. This could certainly explain why government agencies are relatively powerless when it comes to regulating new technologies, and don't require extensive testing before implementation.

Just three years ago, in 2016, a ten-year study was carried out which revealed a significant increase in the number of cancers in rats exposed to cell phone radiation. These findings contradict the widely held assumption that EMF has no harmful effects simply because the mechanism of action has not been understood - the assumption was that because low levels of radiofrequency radiation (below the SAR safety limits for cell phones) do not cause a detectable tissue heating effect, assuming that this heating effect is the only mechanism that could cause damage. This is certainly not the case.

The results of the 2016 study show that as radiation intensity increases, so does the incidence of cancer in rats - a significant dose-response relationship. Of particular importance were the types of tumors the rats developed: high rates of gliomas (tumors in the glial cells of the brain) and malignant schwannomas of the heart. This coincides with at least four epidemiological studies which also establish a link between cell phone use and these types of cancer. None of the rats in the control group developed any of these cancers. It's also important to note that gliomas are a particularly deadly type of cancer. Most people survive only one to three years after diagnosis.

Given the conclusive nature and seriousness of this study, the U.S. National Toxicology Program (NTP) began urging federal agencies to inform the public of these results. Initially, NTP executives stated that they believed these results should be made public as soon as possible because of the high level of risk involved. The FDA and FCC, the two agencies responsible for regulating RF exposure, were notified of the study results, but did not specify how they planned to act on the information. Then, in early 2018, the NTP made an unexplained U-turn and declared that "cell phone use is not a high-risk situation".

A peer review panel of 11 pathologists and toxicologists from academia and industry reviewed the draft reports of the 2016 NTP study and concluded that there is "clear evidence of carcinogenic activity" - "clear" being the strongest of the 5 terms used to classify evidence of carcinogenicity.

Why the NTP is now dramatically downplaying the obvious and undisputed results of this study is a source of much speculation.

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