Sunday, December 9, 2018

44 Reasons Cell Phones Can Cause Cancer

44 Reasons To Believe Cell Phones Can Cause Cancer
Originally Published On
Is there a connection between cell phones and cancer?  Here are 44 reasons to believe that cell phones can cause cancer.
Cell phones emit microwave radio-frequency radiation. Fact.
This radiation has the ability to penetrate our bodies. Fact.
Our governments do virtually nothing to protect us from these dangers. Fact.
And yet there is strong evidence and multiple peer reviewed studies that indicate that cell phones cause cancer and other diseases.
Take a look for yourself at these facts.
But first let's just consider what cancer is.

Cancer And DNA

"Cancer is a term used for diseases in which abnormal cells divide without control and are able to invade other tissues ... all cancers begin in cells ... cells grow and divide in a controlled way to produce more cells as they are needed to keep the body healthy. When cells become old or damaged, they die and are replaced with new cells. However, sometimes this orderly process goes wrong. The genetic material (DNA) of a cell can become damaged or changed, producing mutations that affect normal cell growth and division. When this happens, cells do not die when they should and new cells form when the body does not need them."
So cancer typically involves abnormal cell division and DNA damage and in some cases cells may form a mass of tissue called a tumor.

Types Of Brain Tumor

In the studies done to date cell phone radiation exposures are principally linked to two types of brain tumor: gliomas and acoustic neuromas.
Gliomas, a type of tumor that starts in the brain or spine are typically malignant. Gliomas are particularly deadly. Most people survive only 1 to 3 years after diagnosis.
Acoustic neuromas, though non-malignant (low-grade cancer), are in many cases life threatening given that they are an intracranial tumor.

The 44 Reasons

1. Cellular Damage: Telecoms giant T-Mobile in Germany commissioned an independent study to review all relevant research on the health risks from wireless telecommunications. It was concluded that,
"On the cellular level, a multitude of studies found the type of damage from high frequency electromagnetic fields which is important for cancer initiation and cancer promotion."

Brain Tumors And Brain Cancers

2. Significantly Increased Risk of Glioma:  Gliomas are becoming increasingly common. The $25 million Interphone Study found that:
"... regular use of a cell phone by adults can significantly increase the risk of gliomas by 40% with 1640 hours or more of use (this is about one half hour per day over ten years)."
Source: Table 2 INTERPHONE Study Group. Brain tumour risk in relation to mobile telephone use: results of the INTERPHONE international case-control study. Int J Epidemiol (2010); 39(3):675-694.
3. Tumor Risk on Cell Phone Side of Head: Again from the Interphone Study – currently the big daddy of cell phone radiation studies it being the largest and longest study on the link between cell phones and brain tumors – it also found, "tumors were more likely to occur on the side of the head most used for calling."
4. Harmful Association Between Cell Phone Radiation and Tumors: A review of 23 epidemiological studies by 7 scientists on the link between cell phones and cancer concluded, "harmful association." One of the reports authors commenting the study results said, "although as a whole the data varied, among the 10 higher quality studies, we found a harmful association between phone use and tumor risk. The lower quality studies, which failed to meet scientific best practices, were primarily industry funded."
5. Increased Risk For Glioma and Acoustic Neuroma: the studies performed by the Hardell Research Group are widely regarded as being amongst the best. This recent study finds, "A consistent pattern of increased risk for glioma and acoustic neuroma associated with use of wireless phones." These findings are consistent with their earlier studies.
6. Temporal Lobe & Glioma Risk: A recent French study found evidence of an increased risk of glioma and temporal lobe tumors. The study found that, "risks were higher for gliomas, temporal tumours, occupational and urban mobile phone use." According to EMF watchdog Powerwatch this is an important paper, "that confirms existing studies and which should help move the IARC RF evaluation strongly towards a Group 2A – 'probable human carcinogen'."
7. Increased Risk of Acoustic Neuroma in Long-Term Users of Cell Phones: A recent study on 790,000 middle aged women in the UK found that, "women who used cell phones for ten or more years were two-and- a-half times more likely to develop an acoustic neuroma. Their risk of acoustic neuroma increased with the number of years they used cell phones."
8. Increased Risk of Acoustic Neuroma: Research conducted by Lonn suggests, "an increased risk of acoustic neuroma associated with mobile phone use of at least 10 years' duration."
9. Brain Tumor Risk is Higher on 'Cell Phone' Side of Head:  A research paper that reviewed 11 studies found, "a link between prolonged cell phone usage and the development of an ipsilateral [same side of head as cell phone] brain tumor."
10. Meningioma: This Swedish study looked at adult brain tumor cases diagnosed over a two year period. Although the study concluded that, "no conclusive evidence of an association between use of mobile and cordless phones and meningioma was found." The studies authors did say, "an indication of increased risk was seen in the group with highest cumulative use."
11. Malignant Brain Tumors: Recent work by Hardell looked at long-term use of mobile and cordless phones. In conclusion it was found that, "this study confirmed previous results of an association between mobile and cordless phone use and malignant brain tumors. These findings provide support for the hypothesis that RF-EMFs play a role both in the initiation and promotion stages of carcinogenesis."
Image: Hardell Research Group

Other Cancers And Tumors

12. Cancer of the Pituitary Gland: The pituitary gland, considered by many to be the "master gland" of the body, is a pea sized organ located in the middle of the base of the brain that produces hormones that play a major role in regulating vital body functions and general well-being. This study (already referenced above) also found that,
"the risk of cancer of the pituitary gland more was more than twice as high among women who used a cell phone for less than five years as compared to never users."
13. Thyroid Cancer: The thyroid gland is situated in the neck. Using a cell phone against your ear exposes your thyroid to cell phone radiation. A recent Israeli study observing that, "the incidence of thyroid cancer has been on the rise in Israel for more than a decade which matches the rise in the use of cellphones" collected human thyroid cells from healthy patients and subjected them to radiation. The study found, "evidence of changes in thyroid cells in response to electromagnetic radiation."
14. Melanoma RiskMelanoma is a cancer that starts in a certain type of skin cell. A Swedish study found "a very clear association between increasing use of mobile phones and increasing rates of head melanoma in Nordic countries."
Image: Örjan Hallberg
15. Stem Cell Cancer: In a controversial US study on 29 cases of neuroepithelial tumors, cell phone users accounted for 11 of them. These initial results indicated a near tripling in the risk of neuroepithelial tumors through cell phone use. The published results were revised to reflect a doubling of risk and then reported as not "statistically significant."
16. Oral Cancer: An Israeli study on 460 cases of parotid gland tumors found, "based on the largest number of benign PGT patients reported to date, our results suggest an association between cellular phone use and PGTs [parotid gland tumors]." The parotid is the salivary gland near the cheek where many users hold their cell phone.
17. Parotid Malignant Tumors: Another Israeli study analyzed deaths as recorded on the National Cancer Registry over a 36 year period found, "the total number of parotid gland cancers in Israel increased 4-fold from 1970 to 2006 , whereas other major salivary gland cancers remained stable."
Image: Environmental Health Trust
18. Leukemia: A comprehensive review of over a dozen studies including studies on exposures from cell tower radiation, TV and Radio broadcast towers concluded, "cancer, especially brain tumor and leukemia, but all other cancers also."
19. Lymph Node Cancer: In an Australian study one hundred mice were exposed to RF radiation for two 30-minute periods per day for up to 18 months. The authors called the increased incidence of lymphoma "highly significant." They added that "it is very unlikely that the faster onset of cancer was due to chance."
20. Multifocal Breast CancerAmerican researchers studied four young women with breast cancer. They found that, "all patients regularly carried their smartphones directly against their breasts in their brassieres for up to 10 hours a day, for several years, and developed tumors in areas of their breasts immediately underlying the phones."
21. Eye Cancer: A German Study has established a link between uveal melanoma and cell phone radiation and similar exposures. The study "found an elevated risk for exposure to radiofrequency-transmitting devices."  Another study found ocular symptoms and sensations in long term users of mobile phones.
22. Diverse Cancerous Tumors: A Brazilian Study established a direct link between various cancer deaths such as tumors in the prostate, breast, lung, kidneys and liver in Brazil's third largest city, and cell phone tower radiation exposures. The study found that, "more than 81 percent of people who die in Belo Horizonte by specific types of cancer live less than 500 meters away from the 300 identified cell phone antennas in the city".
Source. This same study also lists more than a dozen other research papers that have found a link between different cancers and cell phone/cell tower radiation exposures.

Cell Phone Subscriptions And Brain Tumors

23. Cell Phone Subscription Link to Brain Tumors: A U.S. study analyzed the number of cell phone subscriptions and brain tumors in nineteen US states, they concluded,
"the very linear relationship between cell phone usage and brain tumor incidence is disturbing and certainly needs further epidemiological evaluation."
24. Brain Cancer Incidence Increases Over Time (U.S): Another U.S. study of brain cancer incidence trends in relation to cell phone use in the United States found, "there was a statistically significant increasing trend between 1992 and 2006 among females but not among males. The recent trend in 20–29-year-old women was driven by a rising incidence of frontal lobe cancers."
25. Brain Cancer Incidence Increases Over Time (Europe): Studies carried out in Norway, Finland and the U.K. have identified a similar trend of an increase in the incidence of brain cancer over time. In the UK study the incidence of malignant brain tumors close to where you hold your phone was highlighted.
Source: Mobile Phone Use and Cancer Risk – Research on a Group 2B Carcinogen. Joel M. Moskowitz Ph.D.

Other Effects On the Brain

26. Blood-Brain Barrier (BBB) Permeability: The BBB is a membrane which prevents toxic materials from the blood from entering the brain. It was first discovered in 1975 that RF radiation causes the BBB to leak, since then at least a dozen laboratories around the world have corroborated this effect. There's no consensus on the link between BBB damage and cancer but some studies elude to this.
27. Brain Cell Loss: A Turkish study on adult female rats that were exposed to a 900 MHz electromagnetic field found that, "EMF exposure caused a significant decrease of the ... cell number ... additionally, cell loss can be seen." In their conclusions the researchers drew parallels between these exposures and teenagers' brains that are exposed to cell phone radiation.
28. Brain ActivityResearchers in China exposed 18 participants to RF radiation (LTE) for 30 minutes which was well within international (ICNIRP) cell phone legal limits. They concluded that, "30min LTE RF-EMF exposure modulated the spontaneous low frequency fluctuations in some brain regions."
29. Brain Blood Flow Affected: This Finnish brain imaging study found that "that the EMF emitted by a commercial mobile phone affects rCBF  [regional cerebral blood flow]  in humans." This suggests that cell phone radiation affects neuronal activity.
30. Texting Affects Memory:  An Australian study on young adolescents found "students who reported making or receiving more voice or SMS calls per week, and in particular more of both, demonstrated shorter response times on learning tasks, but less accurate working memory."

DNA Damage

One way cancer and other diseases are believed to develop is when the DNA (genetic information) in a cell becomes damaged. This damage mutates the DNA.  There are many studies linking cell phone radiation exposures to different types of DNA damage.
31. Single and Double-Strand DNA Breaks: In pioneering work a University of Washington team found DNA single strand breaks from RF radiation exposures on rats in an initial study. A subsequent study found single and double-strand DNA breaks.
32. Various Genetic Effects: An Austrian study analyzed the results of 101 different published articles on the effects of radio frequency EMFs on DNA. The study concluded that, "there is ample evidence that RF-EMF can alter the genetic material of exposed cells."
33. Increased Rates of Micronuclei: Micronuclei proliferation indicates a type of DNA damage strongly associated with cancer. A Brazilian study found that, "electromagnetic field irradiation [low level cell phone type exposures] during pregnancy leads to an increase in erythrocytes micronuclei incidence in rat offspring."  Several studies have found increased rates of micronuclei in the body following exposures to RF radiation.
34. Heat Shock Proteins (HSPs) Production Decreased: A U.S. study exposed chick embryo's to RF radiation. They concluded that, "this EMF-induced decrease in HSP70 levels and resulting decline in cytoprotection suggests a mechanism by which daily exposure (such as might be experienced by mobile phone users) could enhance the probability of cancer and other diseases."
35. Oxidative DNA Damage: The Guler study in Turkey exposed female and male infant rabbits to 1800 MHz radio frequency radiation and found, "GSM-like RF radiation may induce biochemical changes by increasing free radical attacks to structural biomolecules."  Free radical damage is associated with the development of cancer.
36. DNA Strand BreaksThis Austrian study exposed human and rat cells to mobile phone radiation and found, "DNA single- and double-strand breaks."
37. Changes in Gene Expression: The Belyaev study found that, exposing the "rat brain to 915 MHz GSM microwaves induces changes in gene expression." Other studies suggest that, "subtle changes of gene expression associated with [disease]."
38. Genotoxic Effects: The Schwarz study exposed human cells to 1,950 MHz UMTS. It concluded that "UMTS exposure may cause genetic alterations in some but not in all human cells in vitro."
39. Neurotransmitters Impacted: This Bavarian study followed 60 people over one and a half years following the installation of a new cell phone base station in their village. The study concluded that, "the effects showed a dose-response relationship," that it had "occurred well below current limits for technical RF radiation exposures" and that these effects have "great relevance for health and [are] well known to damage human health in the long run." In other words the more people were exposed to cell phone type radiation the bigger the impact on their health.

40. Chromosome Damage: A Belgian study reviewed 16 expert gene monitoring studies from around the world. In 13 of the 16 independent studies performed worldwide it was found that, "RF-exposed individuals have increased frequencies of genetic damage (e.g., chromosomal aberrations)."
41. Central Nervous System: US based researcher Dr. Henry Lai comments that there are several studies which show that repeated RF exposure at relatively low power caused morphological changes in the central nervous system, "changes in morphology, especially cell death, could have an important implication on health. Injury-induced cell proliferation has been hypothesized as a cause of cancer."

Reading Between The Lines

The studies don't tell all of the story. Here are some other things you need to know.
42. Latency Period Before Diagnosis: To put this in the words of researcher Dr. Martin Blank "cancers do not form overnight." In almost all cases, cancerous tumors take many years to form and metastasize." According to Dr. Blank's statements, then cancers are overpowered. This would suggest that we might be sitting on a cell phone radiation cancer time bomb.
43. Cell Phone Radiation Cancer Time Bomb: To give a sense to what this latency period could mean in terms of the incidence of brain tumors in the years to come, researcher Lloyd Morgan produced this alarming graphic showing that brain tumor cases could reach epidemic proportions within the next decade:

44. Flawed Research: Not all of the research points to a link between cell phone radiation and cancer. But then that's hardly surprising given the lengths some researchers go to, to skew the results. This research paper also lays bare the phenomenon of study bias. This can take many different shapes and forms; insufficient latency time, incorrect definition of "regular" cell phone user, cell phones radiating higher power levels in rural areas not investigated, exposure to other transmitting sources not considered, exclusion of brain tumor cases due to death or illness, etc.

The Tip Of The Iceberg

There is lot of interest surrounding the link between cell phone radiation and cancer. But cancer is only the tip of the iceberg.
Microwave radio-frequency radiation exposures of the type emitted by cell phones are also linked to many other diseases and potentially life threatening illnesses, including:
  • sperm damage & male infertility
  • miscarriages
  • vaginal discharge
  • vascular system disease
  • tinnitus
  • childhood cancer
  • sleep problems
  • depression
  • irritability
  • memory loss
  • concentration difficulties
  • headaches
  • dizziness and fatigue
  • suicidal tendencies
  • arrhythmia
  • heart attacks
  • bone marrow interference
  • altered calcium level in cells
  • ADHD
  • reduction in night-time melatonin
  • suppression of the immune system
  • arthritis
  • rheumatism
  • skin symptoms
  • lymphatic diseases
  • autism
  • hearing problems
See more at here
Learn morea bout cancer at the upcoming premiere of The Truth About Cancer®: A Global Quest 9 Part Docu-series Starts Oct. 9th. Save your spot. 

Fasting to Heal Autoimmune Disease

Fasting to Heal Autoimmune Disease: Fasting, a mainstay of virtually every cultural and religious tradition on earth, is an essential tool in the management of autoimmune disease, and should be considered as a therapeutic intervention in autoimmune patients in order to improve both metabolic and immune parameters.

Plague: One Scientist’s Intrepid Search for the Truth About Human Retroviruses and Chronic Disease

Written by Dr. Joseph Mercola


  • A retrovirus is a virus that contains RNA encoded genes rather than DNA. Using reverse transcriptase, the retrovirus is able to transform the single-stranded RNA into a double-stranded DNA
  • When the retrovirus infects a host, it integrates its DNA into the DNA of the host cell, which allows the retrovirus to replicate itself and spread through the host
  • One example of a transmissible retrovirus is the HIV virus, which can cascade into the clinical symptoms of acquired immunodeficiency syndrome (AIDS)
  • A retrovirus family known as xenotropic murine leukemia virus-related viruses (XMRV) may play a causal role in chronic fatigue syndrome, chronic myalgic encephalopathy (ME) and other diseases, including autism
  • Some retroviruses, including XMRV (but not HIV as far as we know), infect your germ cells, which means they are transmitted to your offspring
Judy Mikovits, Ph.D., a virologist, researcher and founding research director of the Whittemore Peterson Institute — which researches and treats chronic fatigue syndrome (CFS) in Reno, Nevada — got embroiled in controversy when, in 2009, she was the senior author on a paper which reported that a retrovirus known as xenotropic murine leukemia virus-related virus (XMRV) may play a causal role in CFS and other diseases, including autism.
Her book, "Plague: One Scientist's Intrepid Search for the Truth About Human Retroviruses and Chronic Fatigue Syndrome (ME/CFS), Autism and Other Diseases," details her research and personal trials that arose as a consequence of her work.
"Kent Heckenlively essentially wrote it," Mikovits says, "because I write like a scientist. We wrote it using the genre of flashback. He taped hours and hours of me telling the story as he asked me questions — because he's trained as an attorney — and then he turned that into this suspense-thriller. Interestingly enough, it almost has to read like fiction because of the lawyers it took to … make sure we weren't sued."

What Are Retroviruses?

Before we go further, let's review what a retrovirus is. A retrovirus is a ribonucleic acid (RNA) virus — in other words, a virus that contains RNA encoded genes rather than deoxyribonucleic acid (DNA). Using reverse transcriptase, the retrovirus is able to transform the single-stranded RNA into a double-stranded DNA.
When the retrovirus infects a host, it integrates its DNA into the DNA of the host cell, which allows the retrovirus to replicate itself and spread through the host. As more and more cells are infected, you become increasingly sicker. Mikovits explains:
"Humans have a DNA genome. Our blueprint is DNA. Retroviruses have an RNA genome, but they also are unique in the RNA family of viruses, where their RNA genome is reverse-transcribed. That is, written backwards by an enzyme unique to retroviruses called reverse transcriptase. That enzyme writes the RNA into DNA.
Then they have another enzyme called integrase. Integrase is like a pair of scissors that cuts open your DNA and then inserts the retrovirus, which is only about 8,000 base pairs, a very, very, very small virus, 50 to 100 nanometers on an electron micrograph. That piece of DNA — called a provirus — is now in the DNA of your cells forever. Every time your cells replicate, you make more viruses."
Now, this DNA insertion has been ongoing throughout human history. According to Mikovits, about 10 percent of the human genome is retroviral in origin. These are called human endogenous retroviruses. These, however, differ in that they've been crippled in part by our DNA methylation machinery (which modulates genes expression and the human immune system — so that they can no longer make complete viruses and therefore cannot infect others.
However, when you're infected with a retrovirus such as human T-lymphotropic virus (HTLV-1), HIV HBRV or Borellia as in chronic Lyme disease and develop DNA methylation and immune dysfunction, these endogenous retroviruses begin to be expressed, and this is yet another really important finding.

HIV — One Example of a Transmissible Retrovirus

One example of a transmissible retrovirus is the HIV virus, which can cascade into the clinical symptoms of acquired immunodeficiency syndrome (AIDS). HIV was discovered in 1982, and as mentioned above, was part of Mikovits' early research work. Her book includes the history of that important discovery.
When Mikovits first began studying retroviruses, HIV/AIDS was completely unknown, but they suspected a retrovirus was at play because of how retroviruses affect the human immune system and lead to acquired immune deficiencies and cancers.
"You don't just one day get this virus and you're sick. In fact, we now know millions of people have HIV and will never develop AIDS. We talk about that in the book, because the book ultimately is one of hope that we fix HIV.
I can honestly tell you in 1999, when I was running the lab of antiviral drug mechanisms, I did not ever expect we would solve that problem. Now, AIDS patients on antiretroviral therapy are probably healthier and develop fewer cancers … than most of the rest of society."
Some retroviruses, including XMRV (but not HIV), also infect your germ cells, which means they not only cause continuous infection in your body but also transfer to your offspring.
"XMRV, the xenotropic murine (mouse) leukemia retrovirus, is the mouse-related retroviruses that cause cancer and lots of neurological diseases. Those affect the stem cells, the egg, the sperm — every cell in your body. That was one of the big 'Oh, my Gods,' about our discovery,"Mikovits says.
When it comes to treatment, the key is to keep the virus silent, because when they're not, each time your cells divide you're making more retroviruses. For this, antiretroviral treatments are used, some of which will be discussed later in this article.


After 9/11, Mikovits started working with a woman whose daughter was severely ill with chronic fatigue syndrome. "Basically, that was the first time I ever saw the disease called ME/CFS," she says.
"This person was looking at a herpes virus known as human herpesvirus 6 (HHV-6). This is a virus prominent in people with Kaposi sarcoma, [which] became associated with HIV and AIDS. Dr. Patrick Moore and Dr. Yuan Chang [discovered] that Kaposi sarcoma was actually caused by a herpes virus — then known as Kaposi sarcoma herpes virus; now, it's HHV-8.
Because the immune system is crippled, you wake up the sleeping herpes viruses. People with autism, ME/CFS and cancers have a lot of chronic active infections, so we often see the Epstein-Barr virus (EBV) associated with outbreaks of ME/CFS …
This woman introduced me to Dr. Dan Peterson and Annette Whittemore in Incline Village, Nevada, where he had been studying outbreaks of ME/CFS for probably 25 years. He said he had a bank of samples. We went up there. I met all the patients.
I interviewed them in great length and developed a hypothesis, which had actually been shown before by Elaine Defreitas, Ph.D., another scientist many years earlier …
Defreitas had isolated retroviruses from patients with ME/CFS. A doctor … named Sidney Grossberg had also isolated retroviruses from at least one patient with ME/CFS. So, the retroviral hypothesis wasn't new. Everything about it fit …
One of the most severely injured patients at that time was Whittemore's daughter, Andrea. That summer (2006), I went up there … and started studying it … I used the systems biology approach, because there's a lot of heterogeneity.
We know AIDS patients who have HIV and will never get AIDS … I interviewed patients in Peterson's office all summer and took blood, urine, saliva and all kinds of samples to isolate that virus, which is what you need to do to show it's associated with a disease."

The Discovery of Infectious Retroviruses

Eventually, she brought together several of her former and current colleagues who were world experts in HIV sequencing to look at ME/CFS. Among them was the world's leading electron microscopist, Kunio Nagashima, who has done the electron micrographs of every family of human retroviruses discovered: the human beta retrovirus, human delta virus, lenti-virus (such as HIV) and gamma retroviruses.
Working in collaboration with the Cleveland Clinic, Mikovits and her team isolated the virus and spent the better part of 2008 and 2009 putting a paper together, proving the XMRV retrovirus was infectious and transmissible and not just another crippled human endogenous retrovirus.
"To our horror, we learned these [retroviruses] could be aerosolized. This was in 2011 … That was really the first nail in my coffin. Pun intended, because the national academy member, John Coffin, Ph.D. — who had told Frank Ruscetti, 'There is no such thing as human retroviruses. Don't study them' — then made a fortune out of HIV and did everything he could to destroy me and the patients," Mikovits says.
"Prior to publication in 2009, we wrote a patent on the detection of these retroviruses, these pieces and parts as contaminants of the cell cultures, of the cell lines from which we make vaccines. After they destroyed my reputation and career and forced the retraction of our paper from [the journal] Science, Coffin turned around and wrote a patent on the detection of these viruses in contaminating cell linings and contaminating biologicals in our labs."
This PDF includes emails, letters and supporting documentation showing how the retraction of Mikovits’ Science paper was forced, after which Coffin filed his own patent for a detection method of the contaminants in cell lines used for vaccines and other biologicals. There’s also documentation detailing the scientific fraud Mikovits asserts in this interview.

Infectious Retroviruses May Contaminate Blood Supply and Vaccines

In her book, she also details how infectious retroviruses are still likely infecting many biological solutions used clinically today, such as vaccines and other therapies. To say that this is a concern would be an understatement. Children’s Health Defense discusses this, and more, in “Looking Back, Looking Forward: Cancer and Vaccines.”1 Mikovits explains:
"That was really at the heart of the big 'Oh, my God.' The worst I learned in this whole experience is how corrupt scientific journals are. In fact, Ruscetti now calls Science, that prestigious journal, 'The National Inquirer,' because they literally engineered the whole thing to destroy MEC/FS patients and any association this virus [XMRV] had with these diseases …
All of the studies showed that the control population was between 3.75 and 6.8 percent infected. When you do a study and there's evidence of infection in 6 percent of the human population, that's 25 million Americans. To put that in context, at the height of HIV/AIDS in 1995, it was 1 million Americans. It would crush our health care system if they had to pay for what they caused."
The result of Mikovits' findings was nothing short of personal devastation. Not only was her paper retracted by Science, she was even arrested for "stealing" her own lab notes. Charges were ultimately dropped, but the damage to her reputation was a done deal.
"Basically, our paper came out on October 8, 2009. It was literally like 'the shot heard around the world.' I was on the road every single day. Everywhere I went doctors were like, 'She's got it. She's got it. She's got it,' and not just with MEC/FS but also with cancer, leukemia, lymphoma, with prostate cancer.
When you start looking at the inflammatory events in the acquired immune deficiencies, with autoimmune disease, with Lou Gehrig's disease, the problem became this [retro]virus. Well, there's no single virus. There's no HIV. There's a whole family of HIVs. There's an HIV 1. There's an HIV 2. There's a strain A, B, C and D.
Why do we do influenza vaccines for this strain de jour or every year? [Because] there are strains of viruses. There are families of viruses … The second that we published this paper, we started working to get a diagnostic test for the blood supply to show it wasn't contaminated, which, in fact, it was.
Later that year, the last talk I ever gave was on a science paper that came out September 22, 2011 … That talk was basically a debate for the evidence that there are human retroviruses of the XMRV family that aren't VP62 (the infectious molecular clone, not the natural isolates of our paper).
We could show in the original paper that there was evidence of murine leukemia viruses, gamma retroviruses that were infectious and transmissible, just as we had said.
Coffin was on the other end of that debate. He said it was all a recombination event. He published a paper in 2013 saying, 'When we worked with mouse cells, they expressed a lot of pieces and parts of retroviruses. This just happened to happen in the laboratory.'
[Hence, he claimed] that's what we had isolated. [Coffin claimed] that what we were looking at were just contaminants in the laboratory. 'It's all a lab contaminant,' [Coffin said], 'You can all go home. You're safe.'"

Massive Public Health Concerns Swept Under the Rug

As one might expect, Mikovits' research caused massive concern in the professional community, because here was a newly identified, infectious and transmissible retrovirus that no one was screening for, and it was potentially contaminating 10 percent of the human blood supply. But rather than face the problem head on, it was rapidly swept under the proverbial rug.
"My mom was watching Good Morning America one morning. Across the bottom of the ticker tape said, 'XMRV all a hoax' … It was horrible. We started to realize our fake news and fake science."
Today, the blood supply is unlikely to be contaminated, thanks to a decontamination procedure developed by a California-based company called Cerus and which Mikovits proved to inactivate XMRV, rendering it noninfectious.
Other biologicals, including vaccines, however, may not be routinely decontaminated using this process, in large part because they’re not required to do so, and drug companies are not liable for vaccine-induced harm. What’s more, decontaminating the vaccine may render it ineffective.
"It won’t work. It will no longer be a vaccine … The Cerus method cleans up Ebola. It cleans up Zika. It cleans up essentially any RNA viruses, including HIV and all three human retroviruses. The Cerus system is extremely valuable to cleaning up the blood supply.
But they cannot clean up the vaccines for another reason. If they do, they prove Andy Wakefield right. They prove me right. They prove they've got 25 million Americans, who they have to support for the rest of their lives and pay damages [to] …"

The Price of Making an Unpopular Scientific Discovery

On a personal level, Mikovits has taken an enormous personal hit. September 29, 2011, she was fired from the Whittemore Peterson Institute for insolence and insubordination, and was driven into bankruptcy after being falsely arrested for stealing her own lab notes. (She never was and to this day is not in possession of her notebooks or any of the two offices full of her work done in her entire career.)
She explains her firing saying that Whittemore had been selling a diagnostic test and the director of their for-profit commercial laboratory was using federal grant funds to do that work (with full knowledge and under the direction of Annette and Harvey Whittemore), which is misappropriation of federal funds. Mikovits became aware of this in August that year, and wrote him off the grant.
"The Whittemores basically fired me immediately in an attempt … to get this scientist, Vince Lombardi, Ph.D. … to recreate the work while I was out of town and say I was a lunatic — that he’d been doing the work all along, and he hadn’t misappropriated any of the funds.
They fired me on September 29 and immediately locked down the entire university to me or my staff … The insolence and insubordination was I had refused a direct order to misappropriate federal funds, basically. I wasn't ever going to do that. The insolence I'm trying to learn not to do, because it probably would have gone a lot better for me if I didn't say 'F-you,' at the same time …
It was September 22, 2011, when I gave my last talk. They had three weeks to get a Science paper out there that would destroy my reputation in the ME/CFS community … Ruscetti had to sign that paper, or he and Sandy Ruscetti would be fired … [and] lose their entire retirement, which is 75 years.
That was one of the few times I sobbed. I was sitting in my bed screaming …It was 6 o'clock in the morning. They were on the East Coast and they needed to get this paper published fast by Science.
I called the Ruscettis and said, "Frank, they agreed to change the language. They agreed to change the title. They agreed it wasn't an association study … [they say] we didn't have a diagnostic test. Either way, the Whittemores are going to kill me because they're selling the diagnostic test.'
So Frank [Ruscetti] signed the paper. They didn't change the wording. [What they did] is pure fraud. Here, the head of the National Heart, Lung, and Blood Institute published pure fraud in the journal Science, just as two years later, Ian Lipkin published pure fraud. It is fake news. It is so corrupt, everything about it.
It's not [the researchers]. It's the top of the line. It's Dr. Tony Fauci. We're only allowed to make incremental advances. When you make a discovery of this nature, it changes all of everything. This is misogyny … This is a bunch of little boys … fighting over who gets credit, while the world dies, while you kill an entire continent.
That's why I do shows like this. Because we're going to teach doctors. When doctors understand the science — and they're coming around a lot — because the science is there. Nothing about our paper, except the sequence of the virus, has ever been wrong. We knew that in the beginning."

Individuals Infected With Retroviruses Should Avoid Vaccinations

According to Mikovits, retroviruses such as XMRV affect entire families, as it can be transmitted to your offspring. Many of these families also have children with autism, which Mikovits believes may be connected to the retrovirus. The question is, what can you do if you’re infected? For starters, Mikovits recommends avoiding vaccinations.
"Until 2011, not inconsequentially, we didn't vaccinate AIDS patients the same way. It's in the book. You don't vaccinate the immune-compromised … By definition, you have an immune system that doesn't work. Why would you vaccinate them? Why would you vaccinate somebody under 3 years old, who has an immune and detox systems that don't work?
This was the key of the RNaseL story (a genetic susceptibility not to degrade RNA viruses), of the Thompson fraudulent paper [Editor’s note: This refers to William Thompson, Ph.D., a former senior scientist at the CDC’s National Center for Immunizations and Respiratory Diseases, who confessed he conspired to cover up links found between the MMR vaccine and autism].
All they had to do was wait for black boys to be 3 years old, and they would have been able to degrade the RNA virus. That's criminal. That's beyond comprehension …
The pearl of wisdom is this DNA methylation. Keep the violent virus silent … DNA methylation has to silence them. You can't inject them in a vaccine. We're injecting millions of pieces in parts of retroviruses in every vaccine, by definition (and admission).
I am working on an ongoing cancer lawsuit that says vaccines cause childhood cancer, a lymphoma. By these same mechanisms, you've destroyed the DNA methylation machinery's ability [to silence the virus]. You've simply overwhelmed the substrate. You've overwhelmed the ability to methylate.
Every time those viruses integrate, you have a better chance at insertional mutagenesis. Don't expose anybody to human (or animal) retroviruses. Use antiretroviral therapy, which are natural products … There are lots of natural products. We published on them. Those are actually therapy for these kids.
[A 100-year-old drug called Suramin] was one of the first antiretroviral therapies for HIV … [It] worked best against the murine leukemia virus-related viruses, against the mouse retroviruses, the gamma retroviruses …
[Dr. Robert] Naviaux [professor of medicine, pediatrics and pathology at University of California San Diego School of Medicine] did a small clinical trial.2 These kids got their life back.3 They started talking again. What did Bayer do? They stopped the trial and took the drug away from everyone. Now, you can't get it …
We could help millions of people get over [autism]. But when you show cure, you know cause. That's it. I would be right … Millions of people would get their lives back, and it's all about money."

XMRV Is a Significant Threat

As mentioned, there are several different retroviruses, which are part of four viral families (delta, lenti, beta and gamma). Aside from HIV and XMRV, there's the human T-cell leukemia lymphoma virus (HTLV-1) family. There are five or six HTLV viruses, but HTLV-1 is the only one known to cause severe disease.
Human beta retrovirus is another virus associated with primary biliary cirrhosis. Many patients with MEC/FS also have family members with primary biliary cirrhosis. As for which one might be the most significant threat, Mikovits believes XMRV is among the most pressing, because while HIV is well-contained at present, XMRV is not, and it appears to play a significant role in diseases of methylation.
Disturbingly, they're now using murine leukemia viruses as vectors for gene therapy and a novel cancer therapy called chimeric antigen receptor (CAR) T-cell therapy. In other words, they're causing cancer and other retroviral illnesses.
"The same thing with Gardasil … We're causing these diseases and we know it because we're using these [retroviruses] as vectors. We don't need infectious viruses. That's one thing that's really important to know. You don't need infectious viruses if you're injecting the provirus, or the pieces and parts. You inject it, past your immunity, past your gut, past RNA cell, past everything. You bypass the immune system. They don't need to be infectious.
All you need is an envelope to cause that prostate cancer. That's a paper that was published 2013. In most of our studies, all we detected was the envelope. The envelope alone causes vasculitis … Another strain of XMRV gamma retrovirus from mice was identified by Gary Owens … associated with cardiovascular disease. This is just a nightmare that we've unleashed in our environment."

Retroviruses and ME/CFS

According to Mikovits, 6 to 8 percent of the general population are infected with infectious and transmissible XMRV-retroviruses, and in the chronic fatigue population, that prevalence shoots up to about 30 to 40 percent. As with HIV, antiretroviral therapies can be very helpful in the treatment of ME/CFS, including low-dose naltrexone.
"You have to silence the other pathogens, so taking care of mycoplasma, taking care of mold, absolutely supporting the gut microbiome [will help]," Mikovits says. "We learned with AIDS and cancer patients that if they don't have the diversity in the microbiome, just like in autism, just like in MEC/FS, it's because the retrovirus is causing leaky gut …
The nonspecific inflammation [is] the retroviruses. If you keep the gut healthy, you can heal. The primary is the diversity in the microbiome, or you can't respond to the drugs. There's a lot of hope. That's what we end the show with. There are therapies. We could fix this tomorrow. That's why I do it."
To learn more, be sure to pick up a copy of “Plague: One Scientist’s Intrepid Search for the Truth About Human Retroviruses and Chronic Fatigue Syndrome (ME/CFS), Autism and Other Diseases,” which reads more like a fictional thriller than a nonfictional book about the science of disease.