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It’s All Enterprise Fraud and Now the Kids Are Taking the Brunt of It: More On mRNA Injections, Lipid Nanoparticle Envelopes, the Liver and the “Anomalous” Hepatitis Outbreak Targeting Our Youngest

06 Sep 22

An article from The Economist grabs our attention respective to a Moonshine piece written back on 08 May 22. It was entitled: RUSSIA, UKRAINE, CHINA and COVID-19: Hepatitis, HIV, COVID-19 and Cancer Weaponized to Target Our Most Vulnerable Population – Children. In it and citing friend and epidemiologist Dr. Lynn Fynn; along with a stack of other second and primary sources, I made a counter-argument to claims made by the CDC about a highly anomalous worldwide outbreak of hepatitis in the very young.

That article is critical contextual backdrop for this piece and is left for your independent consumption. Extracts from it are heavily featured here respective to The Economist.

The Economist begins the dialogue with emphasis added,

In April mysterious cases of hepatitis, an inflammation of the liver, began appearing in children around the world. They were not caused by the hepatitis viruses that typically cause the illness. The World Health Organisation has reported more than 1,000 probable cases in 35 countries. Some children have required liver transplants and at least 22 have died. Researchers have been scrambling to find the cause.

Two studies posted this week on medRxiv, a preprint server, propose an answer—co-infection with two common and usually innocuous viruses, probably helped by certain gene variations in the children who fell ill. SARS-CoV-2 was ruled out as a culprit. One of the infections seems to be from human adenovirus, a common bug in children that causes stomach upsets but does not make them very ill. A cluster of the strange hepatitis cases appeared shortly after a spike in adenovirus infections, though it was unclear what role the virus might be playing, because it is often present in healthy children too.

In the latest research, led by teams at the University of Glasgow and University College London, researchers investigated the blood and livers of 26 children with the strange hepatitis and compared the results with those from more than 100 children of the same age, including healthy children, children with adenovirus but normal liver function, and children with hepatitis for which the cause was known.

Collectively, the two studies found that 25 out of the 26 children with the mysterious hepatitis were also infected with adeno-associated virus 2 (AAV2). This virus (pictured left) was rarely found in the children without that form of hepatitis and, when present in them, it was in much lower quantities.

AAV2 is a parvovirus that cannot replicate on its own but needs assistance from a “helper” virus such as an adenovirus or a herpesvirus. It is not known for causing illness but it is very contagious. Most children are exposed to it at a young age and it lays dormant in the cells, including those of the liver, until infection with a helper virus triggers its replication. The results from the two studies suggest that coinfection by AAV2 and adenovirus—or sometimes possibly a herpesvirus called HHV6, which was found in a few children—is the cause of the mysterious hepatitis illness.

Given how much AAV2 and adenovirus circulate, lots of children probably get co-infected. Why, then, do only a small number of them develop the strange hepatitis? The researchers in Glasgow looked for an answer in the children’s genes. In eight of the nine children with the strange hepatitis they found variations in the Human Leukocyte Antigen gene that were not commonly found in the 58 comparison children. The prevalence of these specific variations is highest in northern Europe—the region where most of the strange hepatitis cases have been reported.

It is unclear how AAV2 is causing the illness. The researchers did not find viral particles in the samples taken when the children were ill, but detected large amounts of RNA traces of AAV2—which suggest that copious replication had happened in the past. This means that an indirect viral mechanism may be responsible, such as an immune reaction to AAV2 that leads, in rare cases, to acute liver inflammation.

The Economist
The Economist

Let’s latch on to meat and potatoes to keep the dialogue manageable. From The Economist, we focus on:

  1. “It’s unclear how AAV2 is causing the illness [hepatitis]”
  2. “Researchers did not find viral particles in the samples when the children were ill”
  3. “[Researchers]…detected large amounts of RNA traces of AAV2
  4. “Large amounts of RNA traces…suggest…copious replication…in the past”
  5. “An indirect viral mechanism may be responsible, such as an immune reaction”
  6. “That leads…to acute liver inflammation

Following this brief introduction, consider the extract below from the first Moonshine article, which will set the counterpoints to the research from The Economist respective to six meat and potato items.

The following timeline is important.

I was positioned to write the very first Moonshine COVID-19 article on 09 Feb 20 once the evidence I began collecting at the beginning of January 2020 was sufficient and adequate to begin making a cogent case that COVID-19 was/is a construct of enterprise fraud. That article focused on pharma patents, patent sharing agreements, COVID-19, George Soros and the first reported effective treatment for SARS-CoV-2, Remdesivir. Today, we know the federal treatment protocol recommending Remdesivir and a ventilator application to be fatal in abundance.

The manufacturer of Remdesivir is Gilead Sciences and so Moonshine set-out in all of this only to learn more about Gilead Sciences and Remdesivir. That was almost 300 articles ago.

By mid-March 2020 and literally before anyone else, I was assuming seemingly wild positions that now read like a factual account of recent history.

For one, I vetted my own research for well over a year and no one was writing; much less evidencing, the positions and analysis. It made it all exclusive in all of the important ways if it bore-out. It bore-out.

For another, I was far enough ahead of the curve that by the mid-March 2020 timeline, I wrote this article: IS COVID-19 A GLOBAL 9/11? EVIDENCE CAN BE ARRANGED TO SUGGEST A FALSE FLAG CONSTRUCT AND HERE’S HOW [this is less than two months after the first U.S. case].

Days later, I wrote: IT’S NOT THE PANDEMIC THAT IT’S IMPORTANT – IT’S THE COVER IT PROVIDES: 24 AREAS FOR CONCERN MAY OUTLINE THE NEXT VERSION OF THE ‘NEW NORMAL’.

Days after that: A PRAGMATIC AND GRANULAR UNDERSTANDING OF HOW AND WHY COVID-19 FUNCTIONS AS A POLITICAL CONSTRUCT – Examining how the enemy operates by comparing COVID-19 to failed impeachment.

Nobody else was writing and evidencing these positions and analysis at the time and for a long while thereafter. People call me crazy now. Y’all should have heard them all then.

I review this history as an introduction because it’s imperative to the analysis, findings and the veracity of the positions and evidence behind what follows.

The point is the origin of it all. The origin thread attached immediately to Soros, Bill Gates and a bunch of others. It was like working center-out from a cobweb and hitting every strand along the way. IT ALL BEGAN WITH REMDESIVIR AND THAT MEANS IT ALL BEGAN WITH GILEAD SCIENCES.

So, almost 300 articles all began with Gilead at the genesis and it has led to questions today aboutthe rare hepatitis cases in children that may be caused by the mRNA injections.

Now watch how the overlays and entanglements unwind. This is from the original article:

From the above, we take note of Gilead’s enmeshment with redundant agencies and entities featured throughout all of our work in addition to the references to HIV, which overlap three critical domains: 1-The heavily patented [40,000] and bioengineered SARS-CoV-2 has six artificial HIV insertions in it; 2-There is direct evidence of COVID post-injection HIV positive tests and 3-There is direct evidence of potentially permanent post-injection autoimmune deficiency branded as VAIDS [HIV-like induced illness by means of injection/infection.] Further evidence for this is found in the annex featured at the bottom of the article.

Here’s another press release from Gilead from 24 Mar 22 pertaining to Ukraine:

Political Moonshine

From it we take away the nexuses that now envelop hepatitis relative to Ukraine via Gilead Sciences. The overlay stitching to The Biden Crime Family, which features Ukraine as one epicenter of corruption, crime and treason and China as the other, threads directly to Ukraine in the context of biowarfare that occurs respective to U.S. Department of Defense biolabs in Ukraine. The linkage is found in Metabiota; it’s the bridge to Biden.

From the same article, stack this on top of everything else [emphasis added]:

From this release [linked in the previous quote], pay particular attention to Gilead’s admission to working on hepatitis in Ukraine because it’s the linchpin for the angle further vectoring in on America’s children right now: “An Update on Ukraine from Daniel O’Day, Chairman & CEO – Working with many partner organizations, we provide treatments and support to help people in the region with various diseases and conditions, predominantly HIV, hepatitis and COVID-19.”

Incredibly and as as we put forth with evidence, it’s the aggregate of HIV, hepatitis and COVID-19 that make our case that the explanations centered on our children are patently disingenuous and further, that the allegation is such that they know exactly what is occurring because likely decades of evidenced research and development underpin it.

Moving on in our roadmap respective to Gilead, we also note how the 1996 treaty was the basis of litigation and settlement involving Gilead Sciences v. Ukraine in 2017 in an unrelated case.

[…]

Aggravating the established fact is the direct link between HIV and hepatitis because they are transmitted in the same way and with patients often times suffering from co-infection. Further,

Political Moonshine

These viruses infect the liver and cause it to become inflamed. When the liver is inflamed or damaged, its function can be affected. Viral hepatitis progresses faster and causes more liver-related health problems among people with HIV than among those who do not have HIV. Liver disease, much of which is related to hepatitis B or C, is a major cause of non-AIDS-related deaths among people living with HIV.

HIV.gov

We know as long evidenced that SARS-CoV-2 and the mRNA injections result in the production of the S1 spike protein, which binds to the Ace 2 receptor found in the body’s most important organs and further, that, “SARS-CoV-2 spike protein disrupts lipid metabolism resulting in liver, heart & kidney damage.” SOURCE

“The liver plays a central role in lipid metabolism, serving as the center for lipoprotein uptake, formation, and export to the circulation. Alterations in hepatic lipid metabolism can contribute to the development of chronic liver disease, such as nonalcoholic fatty liver disease (NAFLD) and add to the progression of other chronic liver disease, as occurs in hepatitis C. Moreover, chronic liver disease can impact hepatic lipid metabolism leading to alterations in circulating lipid levels contributing to dyslipidemia.” SOURCE

Political Moonshine

The key to understanding all of this is the lipid nanoparticle envelope that is tasked with delivering the genetic mRNA payload to the mRNA injection recipient’s cells. I covered the political and Big Pharma entanglements of the lipid nanoparticle envelope respective to the COVID-19 “pandemic” in this recent article: It’s All About the Lipid Nanoparticle Envelope: Wilson Sonsini and the Moderna Case Against Pfizer and BioNTech.

The lipid nanoparticle envelope is critical for these reasons [emphasis added]:

Beyond the obvious thought that Big Pharma is infighting to profit off genocide, here’s what’s really important about all of this [the lipid nanoparticle envelope] and it presents in simplistic form: 1-with no patents for the lipid nanoparticle envelope, there is no “pandemic”, 2-because the first phase of the “pandemic” manifested out of fraudulent data produced by enterprise fraud prosecutable under RICO statute, 3-and that is not a sustainable method as the evidence now shows, 4-and so the second phase of the “pandemic” is built to rely mostly on data aggregated out of the evidenced statistical increase in illnesses and disease that has occurred since the roll-out of the mRNA injections, 5-meaning that SARS-CoV-2 was nothing more than the designed impetus to force mRNA injections on the people and not the ultimate objective, 6-because the true pandemic is evidenced to be one of the vaccinated, 7-with the vaccinated now producing the illness and disease by means of their acquired S1 spike protein production, 8-and this creates the perpetual component to the fraud construct, 9-and all by design with the Martin corpus of work into U.S. patents evidencing that, 10-the SARS-CoV-2 virus, the tests to diagnose it and the “vaccines” to remedy it are all owned by essentially the same people.

If you were looking to establish a closed circle fraud construct to execute a fraudulent pandemic, having ownership of the SARS-CoV-2 virus, the tests to diagnose it and the “vaccines” to remedy it would be required. A complicit, corrupt, witting and treasonous MSM seals the deal for them.

Political Moonshine

From the same article, the picture broadens while it gains clarity [emphasis added]:

Respective to the mRNA injections and in furtherance, we also know that the COVID mRNA injection’s “messenger RNA (mRNA) from Pfizer’s COVID-19 vaccine is able to enter human liver cells and is converted into DNA, according to Swedish researchers at Lund University.” SOURCE

Moreover, “Vaccine researchers had assumed that novel mRNA COVID vaccines would behave like “traditional” vaccines and the vaccine spike protein — responsible for infection and its most severe symptoms — would remain mostly in the vaccination site at the shoulder muscle. Instead, the Japanese data showed that the infamous spike protein of the coronavirus gets into the blood where it circulates for several days post-vaccination and then accumulated in organs and tissues including the spleen, bone marrow, the liver, adrenal glands, and in “quite high concentrations” in the ovaries.” SOURCE

It’s important to pause and remember that mRNA technology is not new having derived from 1999 and forward into the early 2000s respective to Ralph Baric’s work with rabbits at UNC Chapel Hill and Pfizer’s work with canines. Compounding that timeline is the fact that SARS-CoV-2 has been in the public domain for over two decades. Translated, it means “they knew” everything before it happened. Hold onto that. SOURCE SOURCE SOURCE

Notable here relative to the CDC Health Advisory presented below is the linkage found in the adenovirus respective to vaccine development related to SARS and the overlay with hepatitis and the fact that adenovirus antibodies assist HIV, “The COVID-19 pandemic necessitated the rapid production of vaccines aimed at the production of neutralizing antibodies against the COVID-19 spike protein required for the corona virus binding to target cells. The best well-known vaccines have utilized either mRNA or an adenovirus vector to direct human cells to produce the spike protein against which the body produces mostly neutralizing antibodies. However, recent reports have raised some skepticism as to the biologic actions of the spike protein and the types of antibodies produced.” SOURCE

In further aggravation of the fact set, there is a direct correlation between the adenovirus vector, hepatitis and HIV and most notably, the aspect of vaccinations making recipients more vulnerable to HIV, “A modified virus being used in four COVID-19 vaccine contenders — called adenovirus 5 (Ad5) — has been shown to increase transmission of the AIDS virus in the past, the researchers wrote in a “cautionary tale” published in The Lancet medical journal Monday. Adenoviruses — a group of common viruses which can cause a range of illnesses, including the common cold — are sometimes genetically engineered and used to create inoculations. But the Ad5 strain used in a potential HIV vaccination a decade ago was found to make some men more vulnerable to HIV in placebo-controlled trials, according to Science Magzine.” SOURCE

The hepatitis vector parlays into discussions about cancer and the plausibility of COVID causing higher incidence rates of cancer.

Political Moonshine

From the same article, the following brings it altogether with these strongly evidenced correlations and overlays: unprecedented childhood hepatitis world wide, mRNA injections, lipid nanoparticle envelope, adenovirus vectors, SARS-CoV-2 attributes, S1 spike protein production, hepatitis, HIV vectors, HIV artificial inserts into mRNA injections as all central to the LIVER [and more] [emphasis added]:

This is emblematic of the enterprise fraud at hand because there is a significant problem in the empirical data and conclusions about it as evidenced by epidemiologist Dr. Lynn Fynn [posted to her Telegram feed]: “News headlines and mainstream media titles are stating that unvaccinated children are getting hepatitis and liver damage from an unknown cause (or speculating adenoviruses as the cause) but fail to mention that actual case data shows that the WHO classifies children involved in this issue fall under the ages of 0 – 16 years of age, that the majority of cases are in the 1 month – 4 year old age group, and that 100% of the cases in that age range are being active breastfed (or have been breastfed within the last 12 months) by fully vaccinated mothers.” SOURCE

Political Moonshine

Breastfeeding. It’s simple logical deduction: The hepatitis is anomalous because it’s unprecedented in its occurrence and by its rates of infection. This suggests that something was introduced as a catalyst to cause the outbreak. The outbreak timeline comports directly with the introduction of the SARS-CoV-2 virus and the mRNA injections that are directly and strongly correlated by the above overlays that are supported by sound medical and scientific evidence.

It’s been a pandemic of fraudulent data and fraudulent deaths that has turned to actual deaths due to the reverse transcription process occurring in places like liver cells that are reprogramming human DNA to become spike protein producing machines forever.

This means all of the MSM “scientific” explanations that are never cogent or logical are nothing but tapestries of continued cover-up of the narrative to obfuscate the enterprise fraud that is occurring beneath it and the carnage it’s causing.

Friend and epidemiologist Dr. Lynn Fynn delivers the granular evidence in support:

Dr. Fynn also includes further aggravating evidence for the lipid nanoparticle [LNP] envelopes necessary to deliver the mRNA vaccinations linking a report that states, “Intradermal and intramuscular injection of these LNPs led to rapid and robust inflammatory responses, characterized by massive neutrophil infiltration, activation of diverse inflammatory pathways, and production of various inflammatory cytokines and chemokines. The same dose of LNP delivered intranasally led to similar inflammatory responses in the lung and resulted in a high mortality rate, with mechanism unresolved. Thus, the mRNA-LNP platforms’ potency in supporting the induction of adaptive immune responses and the observed side effects may stem from the LNPs’ highly inflammatory nature.” SOURCE

Fynn states, “Judicial Watch today announced it received 466 pages (https://www.judicialwatch.org/documents/jw-v-hhs-fda-pfizer-biontech-vaccine-prod-3-02418/) of records from the U.S. Department of Health and Human Services (HHS) regarding biodistribution studies and related data for the COVID-19 vaccines that show a key component of the vaccines developed by Pfizer/BioNTech, lipid nanoparticles (LNPs), were found outside the injection site, mainly the liver, adrenal glands, spleen and ovaries of test animals, eight to 48 hours after injection.”

Political Moonshine

We return to our six points of focus to provide the evidenced positions:

  1. “It’s unclear how AAV2 is causing the illness [hepatitis]” > Unless AAV2 infections are somehow a product of S1 spike protein production activating dormant viruses found in most children, which compounds the fact that some COVID-19 vaccines are adenobirus-based [“Both Johnson & Johnson’s vaccine and the AstraZeneca/Oxford vaccine use adenovirus vectors. Johnson & Johnson’s vaccine utilizes an Ad26 vector (a human adenovirus) believed to have less natural immunity in the population, Children’s Hospital of Philadelphia reported. The AstraZeneca/Oxford vaccine (called Covishield in India) uses a chimpanzee-based vector called ChAdOx1. This same vector was used in a 2018 trial on 24 people for a MERS vaccine, CEN reported.”] Breastfeeding is the other vector from the vaccinated [recently relative to the child’s birth?] mother to the unvaccinated child.
  2. “Researchers did not find viral particles in the samples when the children were ill” > This is dependent upon breastfeeding.
  3. “[Researchers]…detected large amounts of RNA traces of AAV2
  4. “Large amounts of RNA traces…suggest…copious replication…in the past” > This is suggests dormant viruses that could be triggered to become active by known mechanisms and especially so given that the S1 spike production interferes with liver function causing severe side effects.
  5. “An indirect viral mechanism may be responsible, such as an immune reaction” > “Immune reactions are the analog to adverse reactions suffered post-mRNA injection or post-infection, which is evidenced by Pfizer to transmit through breastfeeding.
  6. “That leads…to acute liver inflammation > As per the explanations given in detail above and especially as it relates to breastfeeding, hepatitis, the liver, mRNA injections, lipid nanoparticle envelopes, reverse transcription, S1 spike protein production and the other defined intersections, overlays and correlations, there is strong evidence that the anomalous hepatitis outbreak is a consequence of mRNA injections and SARS-CoV-2 infection as complicated by a host of other factors including genetic ones and the important vector of breastfeeding.

Dr. Fynn is convinced of it. So am I.

It’s all by design, folks. They knew then like they know now and they continue to lie while explaining it all away to made-up irrational and unfounded science predicated on cooked-up data.

It’s all enterprise fraud, y’all, and now the kids are taking the brunt of it.

Had enough yet?

Democrat, Republican, progressive liberal, conservative, black, white, brown, yellow or other, have you had enough yet?

I bet our kids have… if only they knew.

How tragic.

What have we done, America?

The answer to that question is: Nothing yet.

-End-

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