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May 1, 2020
Dr. Daniel Erickson, owner of seven CA urgent care facilities, was thrown into the spotlight after his press conference on the COVID 19 stirred up enough controversy to get censored by YouTube. Here’s Del’s follow-up interview and this doc’s message is clear: he is not backing down.
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**Comment**
I posted this right after Youtube removed the video but found it on MSN: https://madisonarealymesupportgroup.com/2020/04/28/er-doctors-go-over-covid-19-statistics-why-are-we-in-lockdown-also-a-lesson-on-immunity/
Dr. Erickson talks about Sweden: https://madisonarealymesupportgroup.com/2020/04/25/closing-borders-is-ridiculous-epidemiologist-behind-swedens-controversy-coronavirus-strategy/
https://pubmed.ncbi.nlm.nih.gov/32338290/
The invasive Asian longhorned tick, Haemaphysalis longicornis Neumann, was first detected in the United States in 2017. It has since been found in 12 states, and there is concern that the tick’s parthenogenetic ability and wide variety of host species may allow for broader dissemination. Of the tick-borne diseases endemic to the United States, Rocky Mountain spotted fever (RMSF), a rapidly progressive and potentially fatal disease caused by Rickettsia rickettsii, is the most severe. There is considerable geographical overlap between spotted fever rickettsioses cases, which include RMSF, and the currently known distribution of H. longicornis, providing the potential for this tick to encounter this pathogen.
We have evaluated the ability of H. longicornis to acquire and transmit R. rickettsii under laboratory conditions. Haemaphysalis longicornis as larvae and nymphs acquired the pathogen while feeding on infected guinea pigs. The infection persisted through every life stage, all of which were able to transmit R. rickettsii to naïve hosts. The pathogen was also transmitted at a low frequency between generations of H. longicornis through the ova. While H. longicornis was demonstrated to be a competent vector for R. rickettsii under laboratory conditions, the probability of its involvement in the maintenance and transmission of this pathogen in nature, as well as its potential impact on human health, requires further study.
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**Comment**
The Asian Long-horned tick used to be known as pretty much just a livestock pest. Obviously, researchers are changing their tune. What makes this tick particularly unique and equally terrifying is its ability to reproduce through cloning – making a literal infestation very quickly. It is traipsing through the entire U.S. – having been found in at least 12 states.
Here we see it can also transmit Lyme (although they say “minimally” – whatever that means) https://madisonarealymesupportgroup.com/2019/10/26/researchers-conclude-asian-longhorned-tick-contributes-minimally-to-lyme-disease-in-the-u-s/
The pressing question is what all do they transmit? We know this so far:
It spreads SFTS (sever fever with thrombocytopenia syndrome), “an emerging hemorrhagic fever,” causing fever, fatigue, headache, nausea, muscle pain, diarrhea, vomiting, abdominal pain, disease of the lymph nodes, and conjunctival congestion, but the potential impact of this tick on tickborne illness is not yet known. In other parts of the world, this Longhorned tick, also called the East Asian or bush tick, has been associated with several tickborne diseases, such as spotted fever rickettsioses, Anaplasma, Ehrlichia, and Borrelia, the causative agent of Lyme Disease. https://madisonarealymesupportgroup.com/2018/06/12/first-longhorned-tick-confirmed-in-arkansas/
For a 2016 literature review on SFTS: http://infectious-diseases-and-treatment.imedpub.com/research-advances-on-epidemiology-of-severefever-with-thrombocytopenia-syndrome-asystematic-review-of-the-literature.php?aid=17986
Although the clinical symptoms of SFTS and HGA are similar to each other, but the treatment methods of the two diseases are totally different. Doctors notice that the biggest difference between the clinical symptom of SFTS and HGA is that SFTS patients generally without skin rash, the dermorrhagia is also not seriously, and few massive hemorrhage cases were reported [23]. It is also reported that SFTS patients had gastrointestinal symptoms, such as nausea, vomiting, and diarrhea, which are rarely observed in HGA patients [2]. So these differences can be used as the auxiliary basis of differential diagnosis.
At present, there is still no specific vaccine or antiviral therapy for SFTSV infection. Supportive treatment, including plasma, platelet, granulocyte colony stimulating factor (GCSF), recombinant human interleukin 11, and gamma globulin is the most essential part of case treatment [44]. Meanwhile, some measures were taken to maintain water, electrolyte balance and treat complications are also very important.
Ribavirin is reported to be effective for treating Crimean-Congo Hemorrhagic Fever (CCHF) infections and hemorrhagic fever with renal syndrome, but it is still inadequate to judge the effect of ribavirin on SFTS patients because of the study limitation without adequate parameters were investigated [45]. Host immune responses play an important role in determining the severity and clinical outcome in patients with infection by SFTSV.
For Viral treatment options: https://madisonarealymesupportgroup.com/2016/03/28/combating-viruses/
And lastly, please know ticks parasitize one another, potentially spreading all manner of diseases to humans. This fact also shoots holes in the regurgitated mantra that only certain ticks carry certain pathogens. If they are feasting on one another, they can potentially infect each other and then us: https://madisonarealymesupportgroup.com/2018/03/07/tick-bites-tick-hyperparasitism/
https://madisonarealymesupportgroup.com/2018/07/19/rutgers-racing-to-contain-asian-longhorned-tick/
And now it appears to have the ability at least in a lab setting to transmit RMSF. For more: https://madisonarealymesupportgroup.com/2018/09/14/rocky-mountain-spotted-fever-rmsf/
https://madisonarealymesupportgroup.com/2018/08/16/new-tick-causes-epidemic-of-rmsf/
In 2009, NIAID Director Anthony Fauci was firmly in support of a multibillion dollar H1N1 vaccine project
Today he is an avid supporter of a COVID-19 vaccine.
What he fails to acknowledge is that the 2009 H1N1 Vaccine caused brain damage in children.
It was developed by Glaxo Smith Kline which today is at the forefront of the COVID-19 vaccine initiative.
Dr. Faucy addresses the H1N1 Vaccine Safety Issue in this video (starting at 6:50).
Scroll down for the reports on H1N1 vaccine scam. (Please see link for article)
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**Comment**
Important quote:
Peter Todd, a lawyer who represented many of the claimants, told the Sunday Times: “There has never been a case like this before. The victims of this vaccine have an incurable and lifelong condition and will require extensive medication.”
The vaccine, called Pandemrix, can cause narcolepsy and cataplexy (sudden muscle weakness where you can fall down). Eight hundred children so far have been made ill by this vaccine.
Approx. 30 sec. What cataplexy looks like.
Approx. 6:15 “Diagnosing Narcolepsy”
Notice at about 2:30 the doctor even states immunization can bring on these symptoms – so it’s known that vaccines can cause narcolepsy.
Hopefully it’s clear from these videos that narcolepsy and cataplexy are horrific conditions to live with. GSK was ordered to withdraw Pandemrix in the UK.
The author of the article states the same companies involved in 2009 are at it again by supposedly developing a “safe” COVID-19 vaccine that has been fast-tracked, thereby bypassing important safety protocols. The very same media that was complicit in 2009 are also doing it all over again with COVID-19. Don’t be duped.
Michel Chossudovsky is an award-winning author, Professor of Economics (emeritus) at the University of Ottawa, Founder and Director of the Centre for Research on Globalization (CRG), Montreal, Editor of Global Research. He has taught as visiting professor in Western Europe, Southeast Asia, the Pacific and Latin America. He has served as economic adviser to governments of developing countries and has acted as a consultant for several international organizations. He is the author of eleven books including The Globalization of Poverty and The New World Order (2003), America’s “War on Terrorism” (2005), The Global Economic Crisis, The Great Depression of the Twenty-first Century (2009) (Editor), Towards a World War III Scenario: The Dangers of Nuclear War (2011), The Globalization of War, America’s Long War against Humanity (2015). He is a contributor to the Encyclopaedia Britannica. His writings have been published in more than twenty languages. In 2014, he was awarded the Gold Medal for Merit of the Republic of Serbia for his writings on NATO’s war of aggression against Yugoslavia. He can be reached at crgeditor@yahoo.com
While mainstream medicine and particularly the media confidently blame COVID-19 for every symptom under the sun, the jury is still out on what exactly is causing illness. Since accurate testing was not available in the beginning, a lot of guesswork has been going on. Microbiologist Judy Mikovitz is highly qualified to discuss the matter. Mikovitz calls it the “so-called SARS-CoV-2′ virus. The reason for this is a singular virus does not explain what is being seen in patients.
In the first video (please watch) at about 2:30 Mikovitz mentions Chronic Lyme and the fact many are coinfected with numerous pathogens. She explains this could very well be the reason hydroxychloroquin/Plaquenil and Z-packs are working so well in COVID-19 patients. She also discusses retroviral involvement.
Lastly, Mikovitz says she wants to see the autopsy results of all the people being labeled as dying from COVID-19.
**Please see comment section after article**
Judy Mikovits, Ph.D. is a cellular and molecular biologist,1 researcher and was the founding research director of the Whittemore Peterson Institute that researches and treats chronic fatigue syndrome (CFS) in Reno, Nevada.
She is likely one of the most qualified scientists in the world to comment on this disease because of her groundbreaking research in molecular biology and virology.
Mikovits is absolutely brilliant, but like many gifted researchers, her complex discussions on science quite challenging for the average lay person to follow.
For this reason, I present her interview in a different format, cutting and splicing pieces together to present a more cohesive and coherent presentation of her many important points. I would encourage you to watch the initial, very short, videos first, so you will be well-grounded, and if you are motivated, watch the entire interview at the bottom of this article.
Because there were so many surprising and important revelations in this interview I will present part 2 next week along with an interview with Bobby Kennedy, Jr which will revolve more on the vaccine issue.
One of the most shocking revelations Mikovits reveals is that she doesn’t believe SARS-CoV-2 is the cause of COVID-19 but merely serves to activate or wake up a dormant XMRV infection. To support her assertion, she states that COVID-19 patients have the same cytokine signature as the gammaretrovirus XMRV, which she published many years ago.
XMRV stands for “xenotropic murine leukemia virus-related virus.” Xenotrophic refers to viruses that only replicate in cells other than those of the host species. So, XMRVs are viruses that infect human cells yet are not human viruses.2
The XMRV retrovirus is actually the virus that has the same cytokine storm signature as COVID-19, not coronaviruses, which are far more benign. (I delve into what retroviruses are in another section further below.)
Additionally, there may be other infections that also are contributing to the infection, such as Borelia and Babesia or parasites, which may be why some of the antiparasite drugs like Ivermectin and hydroxychloroquine are working.
Getting back to the issue of gammaretroviruses, Mikovits research showed that many of our vaccines are contaminated with them. How did this happen? In short, vaccine viruses were replicated and grown in animal cell cultures that were already contaminated with retroviruses. In other words, the root of the problem stems from the use of contaminated cell culture lines.
Vaccine manufacturing frequently involves the use of animal tissues and many vaccines are grown animal culture cell lines. As noted in the 2010 paper, “Of Mice and Men: On the Origin of XMRV,” published in Frontiers in Microbiology (which Mikovits did not work on):3
“The novel human retrovirus xenotropic murine leukemia virus-related virus (XMRV) is arguably the most controversial virus of this moment. After its original discovery in prostate cancer tissue from North American patients, it was subsequently detected in individuals with chronic fatigue syndrome from the same continent …
The detection of integrated XMRV proviruses in prostate cancer tissue proves it to be a genuine virus that replicates in human cells, leaving the question: how did XMRV enter the human population?
We will discuss two possible routes: either via direct virus transmission from mouse to human … or via the use of mouse-related products by humans, including vaccines. We hypothesize that mouse cells or human cell lines used for vaccine production could have been contaminated with a replicating variant of the XMRV precursors encoded by the mouse genome.”
Mikovits goes even further, explaining that, “It became clear in 2011 that these [gammaretro]viruses had adapted to become aerosolized.” This is a rather shocking finding, and this, Mikovits says, is what allows the gammaretroviruses to spread in laboratories from one cell line to another.
This could be related to research catalyzed by Charles Lieber, the former head of Harvard’s chemistry department, who is a nanoscience expert and was arrested by federal authorities earlier this year for working with the Wuhan Virology Institute.
Lab workers may also be inadvertently spreading them as they are using cell lines contaminated with retroviruses in vaccine production that could result in the spread of these retroviruses via the finished vaccine. Mikovits suspects COVID-19 may in fact be a type of vaccine-derived or vaccine-induced retroviral infection.
“I don’t believe [COVID-19] is infection from without,” she says. “I believe the spread across [210] countries4 is from injection, and there’s enough evidence to support that.”
Another of her theories is that SARS-CoV-2 is unlikely to have had a zoonotic origin but is likely synthetically produced. She believes it originated in and escaped or leaked from a biosafety laboratory. Mikovits believes both scenarios might be at play, where a lab-created virus, SARS-CoV-2, is causing serious infection and/or death only in those who have underlying retroviruses in their bodies.
Mikovits suspects that people who do not have retroviral infections, SARS-CoV-2 causes no or only mild symptoms. Another possibility is that the SARS-CoV-2 virus is the result of growing coronaviruses in retrovirus-contaminated cell lines, producing a gammaretrovirus-carrying virus. According to Mikovits, her 2009 through 2011 work suggested 25 million to 30 million Americans were carriers of XMRVs and other gammaretroviruses. That estimate is over a decade old now so the number is likely far higher.
“There is a family of gammaretroviruses, most likely [in] contaminated blood supply and vaccines that are still to this day, almost 10 years later, being injected,” she says.
“We don’t need an infectious virus if you inject the blueprint, if you inject the provirus. And … there are a lot of data to support COVID-19 is not SARS-CoV-2 alone, that it’s SARS-CoV-2 and XMRVs (human gammaretroviruses) and HIV.”
“Wearing a mask is going to cause more secretions and give more cells a home and amplify any viruses. [Wearing a mask is] immune suppressive; it’s going to limit your body’s ability to produce Type 1 interferon.
You’re driving the infection in yourself and you’re not preventing the spread. [Instead], you’re amplifying [replication of] not just [SARS-CoV-2] but also many other [viruses], including your XMRVs, influenza or other dormant viruses.
What keeps those dormant viruses dormant? Your natural killer (NK) cells, your mast cells, your macrophages. That’s where you’re getting the inflammatory signature.
So, every virus you amplify is driving the inflammatory signature, and you’re going to get sick. [The resulting illness] doesn’t have to be SARS-CoV-2 at all. You’re making yourself sick [by bringing dormant viruses out of dormancy]. It’s insanity.”
Wearing a face mask after getting a live flu vaccine may further worsen your odds, she says. Why? Because you’re injecting three or more live flu virus strains into your body, which lowers your immune function. You’re also going to shed the viruses contained in the vaccine. If you wear a mask, Mikovits says, you’ll shed those viruses into the mask, which could encourage illness.
On the other hand, not wearing one might jeopardize the health of others. “If you’re shedding [the viruses] into the air, you’re going to make somebody else get another upper respiratory infection that’s going to allow [SARS-CoV-2] to make them sicker,” she warns.
We’re also being lied to about the prevalence of infection. We’re seeing inflated case numbers for the simple reason that the Centers for Disease Control and Prevention no longer requires doctors to do testing in order to confirm that a patient is in fact infected with SARS-CoV-2 or died from COVID-19. The numbers now include “suspected” and “assumed” cases.
As noted by Mikovits, confirming each case through testing matters greatly, as there are hundreds, if not thousands, of microbes that can cause upper respiratory infections, including seasonal influenza viruses. None of those should be lumped in with COVID-19 if we want to understand the true nature and danger of this disease.
What’s more, the initial decision to use RT-PCR (reverse transcription polymerase chain reaction) testing instead of antibody testing was an unwise one, as it virtually guaranteed an overestimation of the problem. RT-PCR is now being used to diagnose an active infection by detecting the presence of SARS-CoV-2 genetic material.5 However, by doing that, you end up with high rates of false positives. Mikovits explains how the RT-PCR test works:
“We’re taking a swab and scraping some epithelial cells [from the back of the sinuses or throat] because that’s what coronaviruses infect … We get a little RNA — because it’s an RNA virus — we reverse-transcribe that, meaning write it backwards with enzymes in the lab, and then we amplify it [through a] polymerase chain reaction …
We’re only taking a piece of the virus, we’re not taking the whole virus … The first thing about [the PCR] test is, it was admitted by the U.S. Food and Drug Administration and the CDC that the tests put out by the CDC were contaminated.
And when you amplify something a million times, or 10 million times — whatever they do in the 30 cycles or so — it’s logarithmic that RNA then is way overestimated … [But] no [viral] particle was identified or isolated from your saliva or from your nasal passages. Nobody took the secretions from your nose or your mouth and isolated the [actual] viruses.
[When I isolated] HIV in 1983, I isolated it from saliva. What you do is you take the virus and grow it in any human cell, in an appropriate cell line, and you make many copies. [Viral replication] means you have [a positive test for] that virus. Then you sequence the whole virus.
A PCR [test, on the other hand] can give you a lot of false positives [by amplifying RNA fragments].
We [also] showed the people that had [HIV] infection had antibodies; that they had been fully exposed and it was not a piece of nucleic acid in a biopsy or in their throat or in their nose. [A piece of nucleic acid] is not a virus. And it’s certainly not infectious.
If RNA is there and in the tiniest amount, I’m not going to cough it on somebody, especially if I’m not coughing. I’m not going to breathe that [out and infect] somebody because there’s no evidence of an infectious virus.”
Rather than using PCR testing, “what should have been done is test for antibodies,” Mikovits says. This is what was done in South Korea. An antibody test will tell you whether you had the infection at some point, and have developed a strong immune response or immunological memory that will allow you to fight the infection should you encounter it again.
“Epidemiology is not done with PCR. In fact, Kary Mullis who invented PCR, Nobel Laureate, and others, said PCR was never intended for diagnostic testing. So that puts that to bed.
It takes nothing to develop a really good serology [i.e., antibody] test … [It takes] a few weeks. It’s pretty easy because the people who have recovered have antibodies. So, you isolate those antibodies, you take their plasma, you purify the antibodies, and then you can grow them.
Then you develop the tests… It’s usually ELISA or Western Blot [which check for] the protein and the antibody binds. You form an immune complex, and you detect it with a dye. You can do that test with a finger stick … and it takes 15 minutes to get the answer, almost like a pregnancy test.”
My belief is that the use of PCR instead of a proper antibody test was intentional, as it inflates the case numbers. Mikovits agrees, saying
“I wouldn’t get any tests right now. I’d simply wash my hands and drink hot lemon water as I always do for any flu season.”
In the Epoch Times documentary, “Tracking Down the Origin of the Wuhan Coronavirus,” Mikovits details some of the evidence supporting the view that SARS-CoV-2 is not a naturally-evolved virus, but rather a laboratory concoction.
One piece of evidence is that the virus contains a protein envelope from the HIV virus. It’s also very similar to SARS which, according to bioweapons expert Francis Boyle, is an engineered bioweapon.
As explained by Mikovits, an Indian paper6,7 detailed the presence of Gp120, a protein envelope from the HIV virus. That paper was quickly retracted due to political pressure. However, Mikovits colleague, Luc Montagnier, made a similar discovery, finding Gp41 in the SARS-CoV-2 virus, which is the transmembrane domain of the HIV virus.
“The folks from India also had GAG. That’s structural proteins. That gives you a clue that it wasn’t a CRISPR technique or a pseudotyping where the envelope was expressed in a gene therapy-type of way. If it were CRISPR, you wouldn’t put the GAG sequences in there.
What was done is, the virus was acquired as they grew SARS-CoV-2 in Vero-E6 cells — the monkey kidney cells where you get HIV.
Simian immune deficiency virus was the origin, and we were told all the way back in the 80s that somebody forgot to cook their food in Africa and a few promiscuous men spread this [HIV] virus around the world. So, you can see again the patterns of the lies and of what people end up believing.”
The addition of this envelope protein from HIV gives SARS-CoV-2 the ability to impair the immune system. It also contributes to its pathogenicity. Mikovits continues her explanation:
“The first thing is, you must grow a virus to make a lot of it. So, you grow it in cell lines. They didn’t take [SARS-CoV-2] from the bat and it jumped into a human. It normally goes through another cell [from] a monkey or a smaller animal. The cell line that supports the growth and expansion [of viruses] are monkey kidney cells.
Maybe [SARS-CoV-2] is not engineered at all … but the end result is, now it not only infects the epithelial cells of the lungs, it infects the white blood cells, it infects the immune cells. We see the splenomegaly in large spleens, we’re seeing penias, cytopenias. We’re losing cells like HIV-killing T-cells …
So, it’s got not only an expanded host range, but also disease symptoms that make no sense for a coronavirus.Hence, we’re killing people because they’re treating an upper respiratory infection, and you’re getting that inflammatory disease signature because you’re infecting the very innate immune response, the macrophages, the monocytes, the natural killer cells, the T cells. And it’s primarily the T-cells in the macrophages because those are the cells HIV 120 and Gp41 infect through CCR5 in the CD4 receptor.
So now you’re going to lose your adaptive immune response, you’re going to drive the inflammation. And it’s the fire [of inflammation] that does the tissue damage.”
Another piece that hints at SARS-CoV-2 being a manufactured virus is the construction of its spike proteins, which bind to ACE2 receptors to gain access into the cell. This appears to be an engineering feature. According to Mikovits, it’s quite clear that the spike proteins came from the original SARS virus, which also infects through ACE receptors.
There are also “single point mutations there that make it far more infectious, easier to spread,” she says, “and how those were acquired, nobody really can say.” At least not yet. Nanotechnology may also have been used to aerosolize it for ease of transmission.
“The nano[size] further increases the host range. So now you can go into every cell. Now you can go across the blood brain barrier. That’s nano. Now you don’t need a receptor. You can breathe it, it can go into every cell of the body. You don’t need the gatekeeper. You don’t need the receptor. You don’t need the lock and key.”
According to Mikovits, one contaminated cell line is the Vero monkey kidney cell line called Vero E6, which was given by Fort Detrick — a U.S. Army Medical Command installation that hosts many of our national biological defense programs and houses the National Cancer Institute laboratory where she used to work — to the biosafety 4 laboratory (BSL-4) in Wuhan, China. This cell line is what the Wuhan lab used to grow and study coronaviruses, she says.
The Vero cell line is listed in the 2015 paper,8 “A SARS-like Cluster of Circulating Bat Coronaviruses Shows Potential for Human Emergence,” co-written by University of North Carolina researchers and Dr. Shi Zhengli, a Chinese virologist at the Wuhan lab who in 2010 published a paper9 discussing the weaponization of the SARS virus.
The contaminated Vero monkey kidney cells were also used in the production of polio vaccines, Mikovits notes. The original polio vaccines were passed through mice brains, as we didn’t have cell lines in the 1930s when that vaccine was originally developed. According to Mikovitz, the spread of this Vero retrovirus has occurred through laboratory workers and hospital caretakers for decades.
“That’s why the family studies we did were so important,” she says, referring to studies in which retroviral transmission was tracked to determine how it spread between family members.10
Alas, whenever patterns were detected, she was always directed to cover them up.
“The patterns are the same as far as the science goes, and the patterns are the same as far as the political corruption, the plague of corruption, in covering up data,” she says.
In 2009, Mikovits got embroiled in controversy when she wrote a paper reporting that a retrovirus known as xenotropic murine leukemia virus-related virus may play a causal role in CFS and other diseases, including autism. I interviewed her about this intriguing and complex story in December 2018 (see linked sentence).
Her career background and past troubles also involved Fauci who, according to Mikovits, is guilty of scientific fraud. She details this in her book, “Plague of Corruption: Restoring Faith in the Promise of Science.”
According to Mikovits, Fauci does not appear to have changed his stripes, and is still misleading the public and hiding the truth about SARS-CoV-2, just like he did with the HIV virus and retroviral-associated diseases.
“I think the way to think about the background of what’s going on right now is to go back to my first interactions with Dr. Tony Fauci when I was a 25-year-old lab technician in the National Cancer Institute. At that time, we had isolated — from blood and saliva — the lymphadenopathy virus.
[Lymphadenopathy-associated virus (LAV)] was the name given to it by Luc Montagnier, the Nobel Laureate, [who] first isolated and discovered that virus and its association with HIV/AIDS.11
In that situation, Fauci delayed the serology testing [to find out] who was exposed [to HIV]. It was politicized such that the only people that were [said to be] susceptible to getting infected with HIV was gay men [and] IV drug users.
The country was told not to worry about it. It was only spread through blood and body fluids and shouldn’t be a problem for most other people. So, the testing that could have been done wasn’t done because of political reasons, and the treatments weren’t done because Fauci had patents, and — we didn’t know this at the time — the wrong type of treatment was used. That led to the spread and [death] of millions worldwide …”
Ultimately, Mikovits and her colleagues discovered that the HIV virus was spread through a contaminated blood supply. After that, they proceeded to look into other “clearly retroviral-associated diseases,” such as CFS,12 certain kinds of autism, cancers, leukemias and lymphomas.
Gammaretroviruses13 are viruses that can cause cancer, leukemia and immune deficiencies in various animals. Examples include murine leukemia virus, feline leukemia virus and mink focus forming virus. As explained in a 2011 paper on gamma retroviruses:14
“Retroviruses are evolutionary optimized gene carriers that have naturally adapted to their hosts to efficiently deliver their nucleic acids into the target cell chromatin, thereby overcoming natural cellular barriers …
Retroviral vectors are fascinating and efficient delivery tools for the transfer of nucleic acids. As a hallmark, all retroviruses are capable of reverse transcribing their single stranded RNA genome into double stranded DNA, which will be stably integrated into the host cell genome.
As highly evolved parasites they act in concert with cellular host factors to deliver their nucleic acid into the nucleus, where they exploit the host cell’s machinery for their own replication and long-term expression occurs.”
The key take-home here is that retroviruses are “integrated into the host cell genome,” and infection can result in “long-term expression.” In other words, once they’re in your body, they can remain dormant, only to reactivate when conditions are favorable. In this regard, they’re quite different from your average virus that, when you’re exposed, invades your cells, replicates and causes symptoms, and is eventually eliminated from your body through your immune response.
In 2009, Mikovits and her team discovered and isolated the first human gammaretrovirus family of retroviruses, known then as XMRVs. As mentioned earlier, XMRV stands for “xenotropic murine leukemia virus-related virus.” Xenotrophic refers to viruses that only replicate in cells other than those of the host species. So, XMRVs are viruses that infect human cells yet are not human viruses.15
(Please see link at top of page for interview)
To reiterate some of the key take-home messages Mikovits delivers in this interview:
• She believes COVID-19 — the disease — is not caused by SARS-CoV-2 alone, but rather that it’s the result of a combination of SARS-CoV-2 (which appears to have been manipulated to include components of HIV that destroys immune function). Previous XMRV (human gammaretroviruses) infection may facilitate SARS-CoV-2 to express the COVID-19 illness.
Put another way, COVID-19 may be initiated by SARS-CoV-2 but dependent upon a preexisting infection with and awakening of other viruses such as XMRV, gamma retroviruses, possibly Lyme and other coinfections, including parasites, and this is why anti-parasitic medications like hydroxychloroquine and Ivermectin help.
• Blood products and vaccines are contaminated with XMRVs that can damage your immune system and cause CFS, cancer and other chronic diseases. The viruses spread within laboratories as they have adapted to become aerosolized, and contaminate cell lines used in vaccine production and other viral research, including research on coronaviruses.
• Flu vaccines have spread a host of dangerous viruses around the world, which can then interact with SARS COV-2.
• It is possible to develop safer oral vaccines, and interferon alpha could be a valuable treatment alternative against COVID-19. Aside from interferons, other treatment strategies discussed in our interview include hyperbaric oxygen therapy, cannabinoids (CBD), peptide T and antioxidant support.
• SARS-CoV-2 is more dangerous and virulent than typical coronaviruses because it includes sequences of HIV, SARS and another virus, which enable it to infect more than just your respiratory epithelium. It can also infect blood cells and hematopoeitic organs such as the spleen.
Last but not least, if this topic intrigues you, be sure to pick up a copy of her new book, “Plague of Corruption: Restoring Faith in the Promise of Science.” You can also find more information on her website, plaguethebook.com.
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For more:
Lyme/MSIDS patients understand this better than anyone. For decades the CDC has INSISTED upon their abysmal 2-tiered testing which is based on blood serology/antibody testing. We understand that many with Lyme many never develop enough antibodies to be picked up upon a test as well as the fact there are numerous strains of borrelia, similarly to coronaviruses having many strains and the ability to mutate: https://madisonarealymesupportgroup.com/2020/03/21/its-not-the-exact-same-virus-everywhere-in-the-world/)
Great read on the limitations of antibody testing: https://madisonarealymesupportgroup.com/2020/04/20/dr-robert-gallo-talked-to-nbc-news-about-whats-needed-in-an-antibody-test-tor-the-coronavirus/
The reason I’m drilling this point home is I’m about three-fourths of the way through “Virus Mania, How the Medical Industry Continually Invents Epidemics, Making Billion-Dollar Profits At Our Expense,” by Torsten Engelbrecht and Claus Kohnlein. This is a MUST-READ book that historically shows repeatedly how there is absolutely no proof that most outbreaks blamed on viruses were even caused by viruses.
Please read this excerpt on how chronic Lyme, due to immune dysregulation, can case retroviral expression.
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 gene 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. https://madisonarealymesupportgroup.com/2018/12/09/vaccines-likely-infected-with-retroviruses-linked-to-chronic-disease/
retroviruses only become harmful when they are exposed to cells from other species, which is what can happen during the vaccine manufacturing process itself as well as during the administration of vaccines that contain cell components from other species. https://madisonarealymesupportgroup.com/2018/03/01/vaccines-could-contribute-to-disease-epidemics-due-to-retrovirus-contamination/
Contaminated vaccines with retroviruses which has been completely squashed by Fauci and Lipkin, is extremely important as COVID-19 patients with retroviruses and/or other chronic illnesses like Lyme (which is a lot of people) are going to worsen after vaccination, in fact James Lyons Weiler, PhD also gives the following chilling prediction:
When Phase I trials become Phase II trials people will start getting infected w/SARS-CoV-2 following vaccination and start dying at even higher rates due to disease enhancement caused by Pathogenic Priming from SARS-CoV-2 vaccination – something the vaccine developers SHOULD have tested for in animal studies, but skipped.
But authorities will blame ONE thing for these deaths: COVID-19. Every single thing is being stacked so that authorities can show high death rates to a virus that has yet to be proven to be the sole cause of illness, let alone death.
When you consider these facts it becomes clearer authorities are not truly interested in pin-pointing how many people are truly ill and truly die from a supposed killer virus.
For more:
https://madisonarealymesupportgroup.com/2020/03/30/the-national-plan-to-vaccinate-every-american/
https://madisonarealymesupportgroup.com/2020/04/29/gates-patent-for-body-activity-data-apparatus/
