21 May 22
The peculiarities of the manifesting monkeypox pandemic compel us to give severely close scrutiny to it against the full backdrop of 31 Dec 19 to the present; the former date representing the first MSM reporting of a viral outbreak in China that would mistakenly come to be known as the “COVID-19 pandemic.” More accurately, the appropriate identifier for COVID is “perpetual construct of enterprise fraud” and it is fully prosecutable under RICO statute.
While the rest of the world was delving into virology, epidemiology, infection, mitigations, etc., as a former fraud investigator, I immediately began working to exclusively evidence what I knew to be an instance of enterprise fraud. Essentially everyone ignored and dismissed those notions as wrong, crazy and otherwise. That was then and this is now. Please be reminded that today is day 140 of year 3 of “flatten the curve” for 2 weeks. Let that sink in for a moment. That’s what perpetual enterprise fraud looks and sounds like.
The copiously evidenced and fraudulent engineering of COVID-19 is the perfect lens for getting in front of what appears to be a reboot of the medical tyranny construct. For proper contextual backdrop moving forward, yesterday’s article should be consumed because it lays the foundation for all that follows: Monkeypox Developments Tie Back to COVID-19, BlackRock and Vanguard, Gives Rise to Extreme Concern Indicating Medical Tyranny Reboot in Enterprise Fraud Scheme.
In the article, I stated that, “We must understand the utilitarian purpose that monkeypox provides. The important aspect of what I’m outlining here is that the virus or impetus being plugged into the enterprise fraud construct matters not whether it be bird flu, monkeypox or something different. What matters is that it is interchangeable in the sense of it being plugged in to drive the construct forward in designed perpetuity.“
The point is that the, “interchangeable new impetus [is now being put forth] to replace the expiring effectiveness of SARS-CoV-2 and its progressive deterioration as a societal control mechanism.”
This should be taken relative to the W.H.O.’s convened emergency meeting over emerging monkeypox as covered yesterday.
As evidenced by COVID-19, the critical aspect for full comprehension is knowing that the enterprise fraud occurs in, “the unilateral emergency determinations processes…and that the fraudulently predicated emergency determinations – first a public health emergency declaration and then a pandemic declaration – permited the issuance of Emergency Use Authorizations that circumvented regular constitutional governance altogether. In short, as SARS-CoV-2 has faded in effectiveness, monkeypox stands to be plugged-in to continue this exact redundant process comprised of the unending renewals of EUAs and the resulting circumvention of regular governance.
We are on the eve of the 22-28 May 22 capitulation to global governance by the illegitimate Biden Administration. For a deeper understanding on a generational timeline extending back to the early 1960s, consider reading this: Predicated By Enterprise Fraud, The “New World Order” and Its Marxist Communist Brand of Global Governance Is Set To Arrive 22-28 May 2022. For anyone finding “new world order,” as being ushered in by medical tyranny, too “conspiratorial,” consider taking Biden’s words over mine,
Along the tenets of psychological warfare, the world’s population has been programmed to react to fear and chaos stimuli for decades and most certainly with regard to COVID-19. In America, the populace subjugated itself to it by divesting itself from its last remaining individual rights an liberties. Monkeypox, perpetual enterprise fraud and medical tyranny have ushered in and will continue to drive the “new world order” that Biden cites; ultimately placing us all on the global plantation. Ergo, we must learn everything we can about monkeypox; the basics being introduced in yesterday’s article.
After uncovering anecdotal and unsubstantiated claims that monkeypox may be a result of or correlated with COVID mRNA injections, extensive research was conducted. The findings here are presented with a full admission that my specialty is fraud; not medicine, virology or epidemiology, and I do not possess the qualifications or expertise to make conclusive findings.
Let’s further understand monkeypox and its direct correlation with smallpox by understanding they both belong to the same genus of orthopoxviruses. Smallpox is caused by the variola virus [VARV] and monkeypox is caused by the monkeypox virus [MPXV.] 
It’s critical to acknowledge that according to the CDC, “The natural reservoir of monkeypox remains unknown,” even though the W.H.O. identifies the likely natural host as, “a range of rodents and non-human primates” while an NIH paper indicates it to be “rodent, sciruidae,” and is generally thought to be carried in such animals as, “African gophers and rodents.” 
With the natural host for monkeypox being unknown, it creates a portal for the plausibility of monkeypox being a bioengineered virus and one that may have received further bioengineering and development in subsequent years; especially after the W.H.O. is stated to have eradicated smallpox as announced on 08 May 1980. This consideration is aggravated by the fact that the monkeypox genesis dates directly to 1958 and the world-wide smallpox eradication plan that began in 1959.
Resting on that premise, now consider the 1958 genesis of monkeypox with a reminder that the first human case didn’t occur until 1970.
Monkeypox was first identified in two monkeys at the State Serum Institute [SSI], Copenhagen, Denmark in 1958. The two monkeys had been received and included in a colony of monkeys said to be crab-eating macaques and they were used for laboratory research    .
During the summer and fall of 1958 two outbreaks of a non-fatal pox-like disease in cynomolgus monkeys have been observed in the monkey colony in this institute. Both outbreaks occurred rather late after the monkeys had been received, ie 51 and 62 days after arrival and only a small percentage of the exposed animals showed signs of illness. Preben von Magnus, Else Krag Andersen, Knud Birkum Petersen, Aksel Birch-Andersen
The monkeypox virus was initially identified and described, “The virus resembles in its properties both variola virus and vaccinia virus.” 
This is the State Serum Institute:
The SSI’s scope and focus is problematic given the uncontested fact that the natural reservoir for the virus that causes monkeypox is unknown:
Moreover, “The establishment of SSI coincided with the international breakthrough within microbiology and immunology. Shortly after, SSI undertook a series of new assignments within the development of other therapeutic antisera, development of vaccines, making of bacteriologic and serologic diagnostic tests, epidemiologic tests and fight against epidemics.” 
After World War II ,
SSI was active in the international tuberculosis campaign managed by Chief Physician, Johannes Holm at SSI. 57m children and young people, most in Central Europe, were tested for tuberculosis by tuberculin produced by SSI, 16m were vaccinated against tuberculosis, and the majority received SSI’s BCG vaccine.
This first international mass vaccination became a role model for WHO’s vaccination campaigns – especially in connection with the extinction of smallpox. Since the campaign and until 2017 SSI has been one of the world’s leading producers of BCG vaccine and tuberculin.SSI
In the 1960s and 1970s ,
In 1951, the Danish childhood vaccination programme was introduced and comprised offers for vaccination against diphtheria, tetanus, smallpox, and tuberculosis.SSI
More recently, the SSI’s webpage indicates that, “Additionally, SSI is responsible for the Danish preparedness against smallpox.”
Oddly if not suspiciously and despite it being the genesis of monkeypox, the SSI’s website search function returns no findings for the search term “monkeypox” :
The eradication of smallpox plays an important role in all of this, “Since the eradication of human smallpox, infections with CPXV have been observed in Germany, but also in other European countries, to an increasing extent. The same applies to monkeypox virus (MPXV) in Africa and infections with VACV-like agents in some regions such as India and Brazil . All these viruses belong to the genus of Orthopoxvirus and are transmitted to humans by contact with infected animals. The observed increase in infections is above all due to the fact that after the vaccinations against VARV were discontinued, the non-vaccinated, predominantly young population was no longer protected against OPV.” 
This indicates some susceptibility to orthopoxvirus infection, including both smallpox and monkeypox, and the W.H.O., CDC, Fauci, et al all now this. This makes orthopoxvirus and specifically monkeypox a plausible biowarfare vector. This will become clearer moving forward.
Recalling what was outlined yesterday, monkeypox and smallpox, which derive from the same genus of orthopoxviruses, are generally regarded as one and the same respective to vaccination. Augment that with the fact that first human case of monkeypox was identified in 1970 in Africa during efforts to eliminate smallpox, which infers vaccination. It led me to ask this question, “If monkeypox first emerged in humans during an effort to eliminate smallpox, which infers vaccinations, and the natural reservoir is unknown, how likely is it that monkeypox is another engineered virus perhaps deriving from smallpox vaccines or somehow correlated with them?”
Recapitulating, the CDC says there is no known natural host for monkeypox, monkeypox and smallpox belong to the same orthopoxvirus genus, the first known cases of monkeypox occurred in 1958 in two monkeys being used for research in a laboratory focused on virology and vaccines, the W.H.O.’s eradication declaration for smallpox led to the end of smallpox vaccinations creating a portal for susceptibility to infection, and the first human cases of monkeypox occurred in 1970 during an effort to eradicate smallpox, which infers vaccination. The recapitulation fully justifies the preceding question.
In light of that and understanding that, “Since the eradication of human smallpox, monkeypox are the most significant OPV infection in humans,” , give further consideration to experimenting with monkeys relative to smallpox, “A natural reservoir of smallpox in non-human primates is thought to be unlikely although further studies are warranted since the survey reveals that certain species of monkeys can be infected with smallpox and that infected monkeys can transmit infection to others. 
Consider this from 2002,
In an experiment unfolding under tight security, six rust and silver monkeys this past week grew listless, refused to eat, and broke out in blisters. Four have become sick, and two have died. The cause: smallpox.
On June 18, microbiologist Peter Jahrling and a team of spacesuited scientists passed through steel doors with key cards, and entered an air-locked laboratory — the “Hot Suite” — at the Centers for Disease Control and Prevention. Their mission: to infect animals with an extinct disease that is now the world’s most feared bioterror pathogen.
The point of the experiment here is to create an animal model of human smallpox. Never before achieved, it is critical to creating 21st-century drugs and vaccines in case of an epidemic. Animal models are systems for testing treatments without endangering human volunteers. Currently, no drugs exist to treat smallpox. And the vaccine to immunize against it, while effective, causes side effects, including death in about three out of every million people vaccinated.UCLA Department of Epidemiology
From the same, the work drew the ire of some contesting the dangerous work down lanes of biowarfare even naming nations; however, no mention was made of Ukraine and the U.S. Department of Defense biolabs in the nation that directly tie to Joe Biden via Metabiota,
Now government health officials have made smallpox drugs a priority of biodefense research, setting off a rancorous debate. Alfred Sommer, dean of the public health school at Johns Hopkins University in Baltimore, calls the animal work “an abhorrent experiment by government idiots.” He warns that it could spark a bioweapons arms race with countries such as Iraq and North Korea. The way to fight smallpox isn’t by injecting monkeys, he says, but by destroying the stockpiles of virus. Dr. Sommer says 18 of the nation’s 29 public-health school deans signed his petition calling for destruction of the stockpiles. This past spring, the WHO and the Bush Administration agreed to preserve the virus until new drugs were developed.UCLA Department of Epidemiology
The work even ties directly to longtime components in our broader body of work: 9/11 and Ft. Dietrick.
After the Sept. 11 attacks occurred, Dr. Jahrling, a senior research scientist at the U.S. Army Medical Research Institute of Infectious Diseases at Fort Detrick, Md., was impatient to follow up work he began a summer ago with an initial experiment on monkeys. For months the 56-year-old researcher waited his turn at the CDC’s only smallpox lab. Finally, he got the green light and hoped to infect monkeys on June 13.UCLA Department of Epidemiology
Noting the correlation to the reference of “intravenous” and vaccines [perhaps mRNA injections],
Dr. Jahrling has courted controversy by giving monkeys as many as one million times the dose that is infectious to humans, and by exposing them in a different way. […] To try to infect monkeys with lethal smallpox last year, Dr. Jahrling double-dosed them with aerosol and intravenous virus, using a super-virulent strain — India I — the strain of choice of former Soviet germ warriors. If anything, it worked too well.UCLA Department of Epidemiology
Moreover and in October 2004 [emphasis added] ,
Federal researchers report they have succeeded in infecting monkeys with fatal smallpox, creating the first animal model of the disease for use in testing vaccines and treatments for humans.
Researchers exposed cynomolgus macaques to high doses of variola (smallpox) virus, causing most of them to die of the hemorrhagic form of smallpox within a few days, according to an online report in the Proceedings of the National Academy of Sciences (PNAS). Scientists previously thought that humans were the only species susceptible to smallpox.
The authors say that the ideal animal model of smallpox would more closely resemble ordinary smallpox in humans, with a longer clinical course and without hemorrhagic manifestations, but would still cause high mortality. They tried to achieve this by giving monkeys lower doses of virus, which resulted in both reduced hemorrhage and lower mortality.
The article says that variola and monkeypox viruses cause very similar diseases in monkeys. Accordingly, the authors hope to test most smallpox countermeasures in the monkeypox model. “The variola primate model would be reserved for testing only those countermeasures that have passed all other FDA requirements for drug or vaccine licensure,” they state.
Analysis of tissue from the infected monkeys has already yielded some information about how smallpox changes gene activity in cells attacked by the virus, yielding clues about how it overcomes host defenses, according to a separate report in PNAS.
“This new research fills in some of the gaps in our understanding of smallpox,” NIAID Director Dr. Anthony Fauci, MD, said in the news release. “Now we are better positioned to speed the development of protective measures.”Center for Infectious Disease Research and Policy
Recall Dr. David E. Martin’s [M-CAM] work correlating COVID-19, SARS-CoV-2, U.S. patent filings and mRNA “vaccine” development to the 2002-2003 SARS outbreak and the 2012 outbreak of MERS, which is in the betacoronavirus genus with SARS-CoV-2, the virus that causes “COVID.”
In consideration of preceding line of evidence thus far, the Oxford/Astra Zeneca vaccines for COVID-19 are positioned front and center beginning with this from Anthony Fauci’s NAIAD and pertaining to rhesus macaques [monkeys] receiving a replication-deficient chimpanzee adenovirus to deliver a MERS-CoV protein [emphasis added],
An investigational vaccine called ChAdOx1 MERS protected two groups of rhesus macaques from disease caused by Middle East respiratory syndrome coronavirus (MERS-CoV). MERS-CoV is a relative of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which causes coronavirus disease 2019 (COVID-19). National Institutes of Health scientists and colleagues are pursuing similar studies with ChAdOx1 SARS2, a vaccine candidate against SARS-CoV-2. They posted their results with ChAdOx1 MERS on a preprint server on April 13. The findings are not yet peer-reviewed but are being shared to assist the public health response to COVID-19.
ChAdOx1 MERS, which uses a replication-deficient chimpanzee adenovirus to deliver a MERS-CoV protein in recipients, also worked against six different strains of MERS-CoV when tested in mice as a single vaccination. Scientists from NIH’s National Institute of Allergy and Infectious Diseases (NIAID) at Rocky Mountain Laboratories in Hamilton, Mont., led the project. Collaborators work at the University of Oxford in the United Kingdom; researchers at the University of Oxford Jenner Institute developed the ChAdOx1 vaccine technology.NAIAD
There was much MSM reporting attributing monkey and chimpanzee components to SARS-CoV-2 “vaccines”as being “Russian disinformation.”
Those claims of disinformation were nothing but disinformation [emphasis added],
AstraZeneca’s vaccine contains a chimpanzee adenovirus genetically engineered to avoid its replication and instead make Covid spike protein in people receiving the jab. The human protein impurities – mostly heat shock and cell scaffold proteins – come from the human kidney cell line used to generate the chimp adenovirus. Viral proteins important for the virus during replication in producer cells were also present.Chemistry World
Additionally [emphasis added] ,
We also had the chimpanzee adenovirus vector from the MERS vaccine, which we’d tested in clinical trials so we knew it was safe and could provoke immune responses. So once we had the sequence of SARS-CoV-2, following its release by Chinese investigators, it was a case of ‘copying and pasting’ the genetic code for the spike protein into our harmless chimp adenovirus to create the ChAdOx1 nCoV-19 vaccine.UK Research and Innovation
In fact and according to an NIH publication, “As discussed above, chimpanzee adenoviral vectors (ChAds) have successfully been used in clinical trials against a variety of diseases.” Further, a PubMed publication establishes the genetic link to vaccinations on a contemporary timeline, “In recent years, replication-defective chimpanzee-derived adenoviruses have been extensively evaluated as genetic vaccines…Expert commentary: The demonstration that chimpanzee adenoviruses can be safely used in humans has paved the way to the use of a whole new array of vectors of different serotypes.”
Recalling that SARS-CoV-2 contains six artificial HIV inserts and according to the CDC, the use of chimpanzee adenoviral vectors extends the work into HIV vaccine development.
Further clouding the chimpanzee adenovirus picture is the fact that adenoviruses pose a risk for monkey-to-human transmission.
As is found with the totality of the enterprise fraud construct mistaken as the “COVID-19 pandemic” and absolutely by design, the manifesting monkeypox pandemic is deeply layered, highly intricate, obtuse, complex and enmeshed; and it collectively makes for very difficult comprehension unless ones occupation is virologist, epidemiologist or similar other.
Even worse, more problematic and as provided to me in private conversation, consider this plausible component to fraud, which is self-explanatory:
Compounding it all in more problematic fashion are the direct parallels to COVID-19 and most notably the chief engineer of pending global governance by means of medical tyranny – the W.H.O. – and its recently convened emergency meeting on the monkeypox outbreak as reported in yesterday’s article.
Another direct parallel is found in the precursory events that serve as dry-run exercises in advance of the formal roll-out of the enterprise fraud construct and associated events. Event 201 was the exercise that preceded COVID-19 and it was a product of the World Economic Forum, Johns Hopkins and The Bill and Melinda Gates foundation. It gives rise to great concern about this, “JUST IN – G7 health ministers to take part in a pandemic exercise in Germany, simulating a fast-spreading and dangerous outbreak of a “smallpox virus” originating from leopards, BILD reports.” – Disclose.tv
Drawing back on old Moonshine relative to 9/11, Dynastic Bush, DHS, emergency declarations, emergency determinations, executive orders, unilateral authority circumventing regular constitutional governance and more,
“These smallpox pandemic simulations are far from the first of their kind. In fact, the Center for Health and Security (“CHS”) already held several of these exercises years even before Event 201. Like the forthcoming pandemic simulation in Germany, CHS’ Operation Dark Winter simulated the ramifications of a smallpox vaccine all the way back in 2001. The case study conducted by Dark Winter coupled with the threat of terrorism manufactured by the US under the Bush Administration to pass the National Security and Homeland Security Presidential Directive more commonly known as Directive 51. This directive outlined the continuity of government that would be enacted in the event of a catastrophe, an action which has been made possible due to an on-going state of emergency reauthorized every 90 days since September 14, 2001 in response to 9/11.Zero Hedge
As a direct overlay to COVID-19 and Event 201, here’s an example of how these exercises play-out recalling our nation’s history of taking exercises live or following them on a short timeline with the same exact but manufactured event. This is from a November 2021 document provided to me in private conversation: Strengthening Global Systems to Prevent and Respond to High-Consequence Biological Threats:
Recalling everything I evidenced yesterday pertaining to the only FDA-approved monkeypox vaccine held by Bavarian Nordic A/S and on the breakneck monkeypox timeline respective to impeccable timing from Biden and the W.H.O., consider this headline relative to a Pfizer-linked company: SIGA Receives Approval from the FDA for Intravenous (IV) Formulation of TPOXX® (tecovirimat)- FDA approval provides an important option for those unable to take oral formulation of TPOXX.
As a former fraud investigator, I’ve spent thousands of hours and thousands of arduously detailed pages stacking-up a mountain of evidence to the moon that irrefutably depicts COVID-19 as a construct of enterprise fraud. In all of that work, I’ve kicked a bunch of dead horses and none more than these: 1-“These people play inside of a box [and that makes them entirely predictable with a tall stack of realized predictions to back it up],” 2-COVID-19 [medical tyranny] will never go away” and 3-“These people will never stop until they are made to stop.”
The problematic timeline is difficult to stomach. On the eve of the process beginning Biden’s capitulation to global governance by treaty, the W.H.O. is driving an apparent manufactured monkeypox construct just as it did with COVID-19; and right down to enterprise fraud components like vaccines, data harvesting, misinformation, disinformation, malinformation and precursory dry-run exercises; all tying to the private sector and NGOs.
As it relates to monkeypox, we can kick those three dead horses again because the evidence indicates that monkeypox is the reboot for the failing SAR-CoV-2 construct; and it’s required to continue driving the enterprise fraud construct that is delivering global governance to the United States and the world over, just like Joe Biden said would happen.