Bump. Fauci is the bernie madoff of medicine.
https://articles.mercola.com/sites/.../is-the-new-coronavirus-created-in-a-lab.aspx
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STORY AT-A-GLANCE
- Cellular and molecular biologist Judy Mikovits, Ph.D. 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 and XMRVs (human gammaretroviruses)
- SARS-CoV-2 also appears to have been manipulated to include components of HIV that destroys immune function along with XMRVs
- Those already infected with XMRVs may end up getting serious COVID-19 infection and/or die from the disease. Mikovits’s research suggests more than 30 million Americans carry XMRVs and other gammaretroviruses in their bodies from contaminated vaccines and blood supply
- Mikovits believes 40 years of data suggest Type 1 interferon at very low dose would be an ideal treatment for COVID-19
- RT-PCR (reverse transcription polymerase chain reaction) testing, currently used to diagnose active infection by detecting the presence of SARS-CoV-2 genetic material, overestimates infection rates. For an accurate account of COVID-19 prevalence, we need to test for antibodies
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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.
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Some details from the interview:
"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.
Vaccine Gammaretroviruses Have Adapted and Are Aerosolized
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 experts 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.”
SARS-CoV-2 — A Combination of SARS, Gammaretroviruses and HIV
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.”
Might Wearing a Mask Worsen Your Odds of Illness?
Mikovits is also highly critical of the recommendation (and in some places mandate) to wear a face mask or fabric cover such as a bandana around your face. She believes:
“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.
