This extensive report attempts to clarify the nature of Covid-19, how it differentiates from other similar viruses, including corresponding similarities of relevance, and seeks to identify the true origins of the Covid-19 virus. It was written in the spirit of scientific inquiry, and as such, the science is never settled. The evidence, ultimately must speak for itself.
In 2010, Dr. Zhengli Shi and her young protégé Dr. Peng Zhou isolated and modified the Corona virus strain found in Chinese Horseshoe bats through reverse engineering and application of adenovirus (ADV) technology, then serially passaged the virus and altered it synthetically: ‘we established a recombinant adenovirus system expressing the S protein from SL-CoV (rAd-Rp3-S) to investigate its immune characterization…the recombinant virus could serve as a potential vaccine candidate against bat SL-CoV infection.‘ Adenoviruses are linked to an array of immune deficiency and acute liver damage in the human body.
In 2010, Dr. Zhengli Shi conducted a study on bats using “An HIV-1-luciferase pseudotype virus carrying the SARSCoV BJ01 S protein,” which demonstrated that the ‘Myotis daubentoni and Rhinolophus sinicus‘ species were susceptible to infection from the SARS-Corona virus after in vitro exposure to HIV, expanding the list of possible ‘candidates as the natural host of the SARS-CoV progenitor viruses,’ The immune system properties in the bat are resilient to the virus, unlike that of humans: ‘the genetic diversity of ACE2 among bats is greater than that observed among known SARS-CoV susceptible mammals.‘ The reservoir in bats is different from humans. Due to their ability to conserve heat, the virus is held at bay in these animals, based on their relative body size and lower body temperature ‘ranging from 18°C to 22°C in summer‘, approximately half that of humans, thus allowing for a higher immunological threshold in bats but a higher susceptibility to viral proliferation in the human body. ‘There is a tight link between individual body size and average minimum temperature of the coldest month, even after accounting for the effects of spatial autocorrelation. These results provide correlative evidence for the role of heat conservation in shaping geographic variation in body size of cave-roosting bats.‘
By 2012, Dr. Zhengli Shi and Dr. Peng ZHou had narrowed the parameters, and inched closer to a common denominator between the Bat strain of Corona and the human infection or SARS. ‘As a highly pathogenic virus, SARS-CoV encodes at least five proteins acting as IFN antagonists, including ORF3b, ORF6, nucleocapsid protein and a number of products of ORF1… With the exception of ORF3b, the bat SL-CoV homologues of these genes share high sequence identities with their SARS-CoV counterparts.‘
In 2015, Dr. Zhengli Shi identified the SPIKE protein in bats as the source of viral transmission, increased immune protection and decreased susceptibility to Corona virus-incurred immune deficiency, respiratory failure and resulting fatality in the bat population: ‘as the spike protein and host receptor are key factors of cross-species transmission of coronaviruses, characterization of the receptor and key binding sites of the spike protein will be important in estimating host tropism of bat coronaviruses and predicting spillover risk.‘
In 2015, Dr. Zhengli Shi perfected the species jumping capability of the SARS-Corona virus at the Wuhan Institute of Virology, a cross-species transmission event, creating a “chimeric” virus far more dangerous than SARS, the bridge to direct human-to-human transmission, which otherwise would have been avoided: ‘we synthetically re-derived an infectious full-length SHC014 recombinant virus and demonstrate robust viral replication both in vitro and in vivo. Our work suggests a potential risk of SARS-CoV re-emergence from viruses currently circulating in bat populations.‘
In 2015, Dr. Zhengli Shi pin-pointed the exact mechanism which exists in Covid-19, which harnesses the ACE2 receptor as an entry point in the human body. ‘We report the isolation and characterization of a novel bat coronavirus which is much closer to the severe acute respiratory syndrome coronavirus (SARS-CoV) in genomic sequence than others previously reported, particularly in its S gene. Cell entry and susceptibility studies indicated that this virus can use ACE2 as a receptor and infect animal and human cell lines. Our results provide further evidence of the bat origin of the SARS-CoV and highlight the likelihood of future bat coronavirus emergence in humans….In conclusion, we isolated and characterized a novel bat SL-CoV isolate, WIV16, which is the closest ancestor to date of the SARS-CoV.’
In November of 2017, Dr. Zhengli Shi admitted to a high probability that “sequential recombination events” led to the emergence of SARS. What she doesn’t address is the reason behind the genetic reshuffling of the virus, that nature itself does not purposefully allow for a sudden recombination without some form of intervention, a significant environmental shift of some kind. The laboratory experiments being conducted on the virus fit the definition of a “recombination event” and clearly caused alternations to the RNA’s template. ‘SARSr-CoVs circulating in this single location are highly diverse in the S gene, ORF3 and ORF8. Importantly, strains with high genetic similarity to SARS-CoV in the hypervariable N-terminal domain (NTD) and receptor-binding domain (RBD) of the S1 gene, the ORF3 and ORF8 region, respectively, were all discovered…We hypothesize that the direct progenitor of SARS-CoV may have originated after sequential recombination events between the precursors of these SARSr-CoVs. Cell entry studies demonstrated that three newly identified SARSr-CoVs with different S protein sequences are all able to use human ACE2 as the receptor, further exhibiting the close relationship between strains in this cave and SARS-CoV. This work provides new insights into the origin and evolution of SARS-CoV and highlights the necessity of preparedness for future emergence of SARS-like diseases.‘
In March of 2018, Dr. Zhengli Shi and Dr. Peng ZHou laid out the STING function in bats which insulates them from the Coronavirus infection, ‘We have demonstrated that bat STING is less active in IFN induction and pinpointed residue 358 as the key site of difference between bat and human STING..‘ They can harbor the virus, they are a reservoir for the infection, but, unlike humans, they do not succumb to it. ‘We demonstrate that bats have a dampened interferon response due to the replacement of the highly conserved serine residue (S358) in STING, an essential adaptor protein in multiple DNA sensing pathways. Reversing this mutation by introducing S358 restored STING functionality, resulting in interferon activation and virus inhibition.‘
Recombinant viruses like Covid-19 solely dwell in a Petri dish, and are transmitted intentionally. They are redeposited into a multitude of viral vaccines, or transported directly by lab personnel outside the confines of the unit. However, they do not exist in the wild environment, unless an infected host animal comes in contact with an animal previously cross-infected in a lab, or else contaminated DNA/RNA material from the source lab spreads and comes in contact with a human. Any spill-over event involving viral transmission from a recombinant virus borne in a laboratory horizontal would have to be deliberate. The popular theory that a zoonotic spread of Coronavirus from bats to humans led to the SARS outbreak in 2003 has never been definitively proven. In fact, it nearly impossible in nature for such a species leap to occur merely by chance. Even more so, the speculation in medical circles, reinforced by the mainstream media that hybrid strains of Coronavirus might have been spread through an intermediate host or circulate in an open wet market-type environment is equally erroneous. This was confirmed in a formal letter published in January 2018 by Dr. Zhengli Shi. ‘The 2.7% seropositivity for the high risk group of residents living in close proximity to bat colonies suggests that spillover is a relatively rare event…this study further supports the notion that some bat SARSr-CoVs are able to directly infect humans without intermediate hosts, as suggested by receptor entry and animal infection studies.‘
Covid-19 was hatched in laboratory, based almost entirely on a decade of experiments conducted by Dr. Zhengli Shi at the Institute of Virology in Wuhan, China. It has been reformulated from the SARS-Corona virus into something much more virulent than its predecessor. It contains an unusual HIV Aids sequence which was added in 2010. ‘Researchers have found shocking similarities between the Wuhan coronavirus and HIV and Ebola. These mutations suggest the virus is manmade.‘ There is no adequate explanation for the mysterious appearance of HIV Aids in the nucleotide sequencing of the Coronavirus, existing outside of the laboratory environment. It is not natural and there is no zoonotic explanation for this anomaly occurring.
The Ebola virus exhibits the same T-cell disrupting characteristics found in HIV-Aids. ‘The glycoprotein (GP) of Zaire ebolavirus (ZEBOV) contains a highly conserved consensus sequence for the subtilisin-like endoprotease furin. The glycoprotein (GP) of Zaire ebolavirus (ZEBOV) contains a highly conserved consensus sequence for the subtilisin-like endoprotease furin. Furin cleavage was therefore considered an important determinant of Ebola virus virulence.‘ The trigger factor lurking in Ebola which generates virulence and accelerates immune dysfunction and lethal impact on the body is HIV. ‘The virus displays a trimeric glycoprotein (GP1,2) on its surface that is solely responsible for membrane attachment, virus internalization and fusion. GP1,2 is expressed as a single peptide and is cleaved by furin in the host cells to yield two disulphide-linked fragments termed GP1 and GP2 that remain associated in a GP1,2 trimeric, viral surface spike. After entry into host endosomes, GP1,2 is enzymatically cleaved by endosomal cathepsins B and L, a necessary step in infection. However, the functional effects of the cleavage on the glycoprotein are unknown…The results also suggest that an additional endosomal trigger is necessary to induce the conformational changes in GP1,2 and effect fusion. Identification of this trigger will provide further mechanistic insights into ebolavirus infection. Here we demonstrate by antibody binding and peptide amide hydrogen-deuterium exchange mass spectrometry (DXMS) that priming of the GP1,2 ectodomain and endosomal pH themselves are insufficient for triggering the conformational changes necessary for fusion, and that an additional trigger must be required in the infected cell.‘
HIV and Ebola symptoms were interchangeable. ‘We examined HIV and hepatitis C virus (HCV) antibody prevalence among suspected EVD cases from the Sierra Leone-China Friendship Biological Safety Laboratory during the epidemic in Sierra Leone. HIV and HCV antibodies were tested in 678 EVD-negative samples by enzyme-linked immunosorbent assay. A high HIV prevalence (17.6%) and low HCV prevalence (0.22%) were observed among the suspected cases.’
‘It has been reported that there is structural similarity between EboGP (Ebola virus envelope glycoprotein) and retroviral envelope proteins and the EboGP-pseudotyped lentiviral vector has been generated for various research.’ A cross section of Covid-19 reveals SARS, Ebola, a synthetic variant of SARS-Corona. The one constant remains HIV-Aids. This is not an environmental phenomenon. What was Aids doing there in the virus in the first place? There is no clear explanation as to why the government would purposefully plant a bio-weapon subjecting its citizens to catastrophic suffering, unless the people were considered expendable, sacrificed as a means to an end, or else the ramifications of the outbreak were not carefully anticipated.
A new study, published March 12th, 2020, on 452 people with COVID-19 reveals 286 harboring HIV AIDS-like symptoms. ‘Of the 452 patients with COVID-19 recruited, 286 were diagnosed as having severe infection. The median age was 58 years and 235 were male. The most common symptoms were fever, shortness of breath, expectoration, fatigue, dry cough, and myalgia. Severe cases tend to have lower lymphocyte counts, higher leukocyte counts and neutrophil-lymphocyte ratio (NLR), as well as lower percentages of monocytes, eosinophils, and basophils. Most severe cases demonstrated elevated levels of infection-related biomarkers and inflammatory cytokines. The number of T cells significantly decreased, and were more impaired in severe cases. Both helper T (Th) cells and suppressor T cells in patients with COVID-19 were below normal levels, with lower levels of Th cells in the severe group. The percentage of naive Th cells increased and memory Th cells decreased in severe cases. Patients with COVID-19 also have lower levels of regulatory T cells, which are more obviously decreased in severe cases.‘
According to the Washington Post, ‘Nearly 25,000 email addresses and passwords allegedly from NIH, WHO, Gates Foundation and others are dumped online.’ This apparently includes sensitive email addresses linked to the Institute of Virology in Wuhan, China. One of the emails uncovered reveals that on the date October 19th, Dr. Zhengli Shi was caught on CCTV camera in Wuhan, exiting a bus and depositing a suspicious block of dry ice right under the main air vent which feeds into the notorious wet-market in Wuhan: The location was a convenient nexus point not only to the market but, in light of the train station, a conduit to the outside world beyond the locale. ‘On the 19th of October 2019, Dr. Zhengli Shi took a bus from Wuhan’s Institute of Technology to the (real location of the the) P4 lab, roughly 16 miles. She stopped one time half way through her journey, opened her suitcase and placed a block of contaminated dry ice near an air vent at the fish market in question. This particular market was chosen because its’ in the same building as hub of world’s largest high-speed rail network, and because it was not outside of her regular route of travel. The event was captured on CCTV.’
The information indicates the Corona virus is airborne, a factor which has since been corroborated, ‘At two hospitals in Wuhan, China, researchers found bits of the virus’s genetic material floating in the air of hospital toilets, an indoor space housing large crowds, and rooms where medical staff take off protective gear…The researchers, led by Ke Lan of Wuhan University, set up so-called aerosol traps in and around two hospitals in the city that was home to the pandemic’s first steps. They found few aerosols in patient wards, supermarkets and residential buildings. Many more were detected in toilets and two areas that had large crowds passing through, including an indoor space near one of the hospitals.’ Severe acute respiratory syndrome and the Ebola virus exhibit a similar airborne propensity.
2b. ‘Under conditions of the current study, transmission of ZEBOV (Zaire Ebola Virus) could have occurred either by inhalation (of aerosol or larger droplets), and/or droplet inoculation of eyes and mucosal surfaces and/or by fomites due to droplets generated during the cleaning of the room. Infection of all four macaques in an environment, preventing direct contact between the two species and between the macaques themselves, supports the concept of airborne transmission…the presence of Ebola virus antigen in some of the respiratory epithelial cells in the lungs of all macaques suggest that the airways were one of the routes involved in the acquisition of infection, consistent with previous reports..‘ National Centre for Foreign Animal Disease & National Microbiology Laboratory, Winnipeg, Canada 05 November 2012
Dr. Xiangguo Qiu, another prominent Chinese virologist, was instrumental in developing Ebola drug treatment. Her husband and colleague microbiologist Dr. Keding Cheng is an expert on Aids. ‘Their quest for an Ebola treatment began in 2005 when Dr. Qiu, a medical doctor from China who came to Canada for graduate studies in 1996, started working on the antibody treatments.’ The timeline is crucial in piecing together the evidence. ‘Ever since 2006, she has been studying powerful viruses—Ebola most of all—at the NML. Both of the viruses that were surreptitiously shipped from the NML to China were studied by Qiu in 2014 (as well as other viruses, including Machupo, Junin, Rift Valley Fever, Crimean-Congo Hemorrhagic Fever, and Hendra). But she paid greatest attention to Ebola for the entirely legitimate aim of developing effective prophylaxis and treatment for the infected…Inevitably, Qiu’s work included a variety of Ebola wild strains—among them the most virulent, which has an 80% lethality rate—and relied heavily on experimental infection of monkeys, including via the airways.’ Canada and China were collaborating (or in competition) on Ebola research, in pursuit of a piece of the market, Dr. Qui and Dr. Cheng were pivotal in advancing that work. ‘Under Kobinger’s leadership, the pair developed “monoclonal antibodies” that have shown promise against deadly Ebola. Their discovery comprises two of three elements in ZMapp, a drug being developed by a California company, Mapp Biopharmaceutical Inc. It has yet to receive regulatory approval.‘ At this stage their intentions seemed transparent and legitimately aimed at furthering the science.
- ‘HIV VLPs can facilitate DC and macrophage targeting and induce more potent immune responses against HIV.‘
- ‘We evaluated, optimized, and encoded 23 different fully human DNA-encoded monoclonal antibodies (DMAbs), which originated from EVD survivors, as well as the ZMapp antibodies.‘
- ‘ZMapp™ had been granted orphan drug status by the U.S. Food and Drug Administration in August 2014 and achieved FDA “Fast Track” status in September 2015.‘
- ‘The chimeric MIL77E mAb cocktail is produced in engineered CHO cells and is based on mAbs c13C6 and c2G4 from ZMapp.‘
- ‘Investigators compared the number of deaths in each group at 28 days after enrollment. Thirteen deaths (37 percent mortality) were reported in the group of 35 patients who received the optimized standard of care only, while eight deaths (22 percent mortality) occurred in the ZMapp group of 36 patients.‘
- ‘They would either receive “optimized standard of care”—the control group—or that intervention plus three intravenous infusions of ZMapp spaced 3 days apart. In the end, the waning epidemic forced the team to end the study late last month after enrolling only 72 people.One participant was “lost to follow up,” Davey explained, and of the remaining 71, 21 died: 37% in the control group versus 22% in those who received ZMapp. “One has to choose one’s adjectives carefully,” Davey said. “This is certainly suggestive of a trend in favor of the ZMapp containing arm.” But the results were not statistically significant.‘
- ‘Here we provide structures of every mAb in the ZMapp cocktail, as well as additional antibodies from the MB-003 and ZMAb cocktails from which ZMapp was derived, each in complex with the Ebola glycoprotein. The set of structures illustrates sites of vulnerability of Ebola virus, and importantly, provides a roadmap to determine their mechanism of protection and for ongoing selection and improvement of immunotherapeutic cocktails against the filoviruses…ZMapp is able to neutralize previous virulent strains of Ebola (Kikwit outbreak 1995), as well as the current West African 2014 strains.‘
“I am concerned about the ethics of providing ZMAPP to Ebola patients before it is tested in animals (invivo) and human beings (clinical trials). My main concern is about the safety profile, dosage and efficacy of ZMAPP in human beings in the absence of both pre-clinical and clinical data.” Francis Masiye, Malawi University of Science and Technology
Dr. Qui and Dr. Cheng were invited to collaborate with Canadian medical researchers, and share expertise on Ebola at Canada’s only official level-4 bio lab in Winnipeg, culminating in their March of 2019 report. ‘Our findings that EboGP-pseudotyped HIV VLPs induced increased NF-κB signaling in U937 cells compared with EboGPΔM-pseudotyped HIV VLPs suggests that DC/MDM-targeting and/or the immunostimulatory effects of EboGP could improve the ability of DCs and MDMs to enhance the adaptive immune response. However, a limitation of the study was that NF-κB signaling was only studied in a U937 cell line and not DCs harvested from immunized mice.‘ On July 5th, 2019, Dr. Qui was caught stealing intellectual property data and immediately thrown out, along with a team of Chinese medical students, by the RCMP. This sudden turnaround indicates she was being professionally disingenuous, which raises immediate red flags. What had she stolen and how long had the leak been going on? There is every likelihood that Qui and Cheng were working on behalf of the Chinese government. ‘Qui made at least five trips over the academic year 2017-18 alone to the above-mentioned Wuhan National Biosafety Laboratory of the Chinese Academy of Sciences, which was certified for BSL4.‘ Given the sensitive material contained in the lab, and the suspicions raised by her travel itinerary, any number of medical secrets could have been taken. But for what purpose? Altruistic or criminal? ‘The lab works in a wide range of biomedical fields. Qiu is known for helping develop ZMapp, a treatment for Ebola virus that was fast-tracked through development during the 2014–16 outbreak in West Africa. She has repeatedly been honored for her work on that project, including with a Governor General’s Innovation Award last year.‘ The Canadian Government certainly didn’t suspect Qui, since she had been given unrestricted access to the bio-lab’s library of resources for several years. It was subsequently learned that the Chinese Medical students were affiliated with designated military facilities and programs centered on biological weapons development, including the Institute of Virology in Wuhan. .
The premise for the origin of Covid-19 encompasses the following: Nobody in the scientific community had more expertise or unlimited access to level 4 bio-labs than Dr. Zhengli Shi, Deputy-director of the Institute of Virology in Wuhan, which stockpiles ‘more than 1,500 strains of deadly viruses’ This enclosed setting presents ample opportunity for “spillover events.” ‘The lab is said to have three testing rooms, two animal storage rooms, one virus bank and one animal-dissection room. Twenty-four scientists can work there at the same time.‘ She conducted extensive research on the SARS/Corona virus for a decade, splicing, and reverse engineering hybrid strains via multiple species to produce an eventual highly contagious “chimeric virus” capable of causing rapid respiratory infection in humans. Dr. Shi is considered a preeminent expert on synthetic application of the SARS virus, cross-species manipulation of the virus.
Overseas in Winnipeg, Dr. Qui and her partner Dr. Cheng exploited available medical research at the facility to study every component of Ebola and its relation to HIV. It was during the summer of 2019 that they proceeded to integrate the HIV component. by splicing Ebola into the hybrid SARS-Corona virus, altering the genomic structure of the virus altogether. The shipment was then returned to China, whereupon it was handed over to Dr. Shi. Over the next several months she finalized the recombinant sequencing of the virus, and upon completion, then acted as the courier to deliver the payload of the Corona hybrid out into the environment on October 19th. This is my hypothesis based on the circumstantial evidence which has presented itself.
There is a strong US connection to the origins of Covid-19, with major financial flowing ties from the National Institutes of Health, an entity of the US Government. and international collusion at the highest levels of the medical establishment. The question remains nebulous as to what extent the research support lent from the Harvard medical center in Boston had on the development of the final version of Cocvid-19. We know that Dr. Charles Lieber, who is chair of Harvard University’s Department of Chemistry and Chemical Biology, right at the center of the controversy holds the key, having been ‘accused of lying about working with several Chinese organizations, where he collected hundreds of thousands of dollars from Chinese entities. According to court documents, Lieber’s research group at Harvard had received over $15 million in funding from the National Institutes of Health and the Department of Defense, which requires disclosing foreign financial conflicts of interest. The complaint alleges that Lieber had lied about his affiliation with the Wuhan University of Technology (WUT) in China and a contract he had with a Chinese talent recruitment plan to attract high-level scientists to the country. He was being paid $50,000 per month by the Chinese university and given $1.5 million to establish a nanoscience research lab at WUT, the complaint said.‘
Simultaneously, there were two Chinese nationals caught in Boston working at the medical facility under false pretenses with ties to the Chinese government. Again, all the evidence points to a conspiracy and an intentional cover-up from the outset. It appears this was about damage control, and that the public have not been shown all the evidence. Also, one of the US doctors at the Harvard Medical School who collaborated on the 2015 study ‘A SARS-like cluster of circulating bat coronaviruses shows potential for human emergence.’ out of Boston, along with Dr. Shi at the Institute of Virology in Wuhan, leading to the eventual “chimeric virus” resembling Covid-19, Wayne Marasco, MD., PhD. owns a patent (US20160185865A1 – ‘Affinity matured anti-ccr4 humanized monoclonal antibodies and methods of use‘), and theoretically stands to gain from the development of a drug treatment plan for the Coronavirus. ‘Several companies are preparing to start clinical trials with an antibody-based Covid-19 drug, and several project they could be available by the fall. “A lot of people believe that this could be a bridge to a vaccine. And monoclonal antibodies are the number-one grossing drugs on the market today, so it’s not far-fetched.”‘
The US and Canadian Government have attempted to gain a strategic advantage and capitalize on the SARS-Corona research race, gambled with the Chinese government, allowing them unprecedented access to western technology, a risky strategy which has backfired. They have since been defecting political attention away from the scandal in a deliberate attempt at damage control.
Recently, a former CCP member turned whistleblower publicly refuted the standard party line from the Chinese govt, dismissing it as propaganda. Dr. Li-Meng Yan, a virologist, now living in exile in the west, claims she did some of the earliest research into COVID-19 at the Institute of Virology in Wuhan. “It comes from the lab — the lab in Wuhan and the lab is controlled by China’s government. The first thing is the [meat] market in Wuhan is a smokescreen and this virus is not from nature.” If she is not silenced or arrested in the coming months, Yan’s testimony could be the key to pinning down the perpetrators of this horrendous crime once and for all for the world to see. The truth must come out.
The SARS vaccine has proven ineffective in treating patients diagnosed with Covid-19, and succeeded in co-infecting the vaccinated population with the SARS virus. At the time, in 2003, it was believed the source of SARS threat lay in the spike protein. However, they did not anticipate the fact that SARS, like Ebola and Corona, does not behave like typical viruses found in the environment. SARS was undoubtedly conceived in lab, but it remained a primitive design, and failed to spread beyond a generally localized epicenter in China and elsewhere. ‘This was found to be a novel nucleocapsid protein that matched almost exactly one predicted by an open reading frame in the recently published nucleotide sequence of the same virus isolate (>96% coverage). A second viral protein corresponding to the predicted 139-kDa spike glycoprotein has also been examined by MALDI-TOF MS (42% coverage). After peptide N-glycosidase F digestion, 12 glycosylation sites in this protein were confirmed…The Spike Protein S—The spike protein is a major target of the cellular immune response to coronaviruses and plays an important role in the initial stages of infection. It mediates the attachment of the virus to the cell surface receptors and induces the fusion of the viral and cellular membranes.‘ Covid-19 is another entity altogether, a vastly more virulent recombinant design in that sense, based on the intricacy of its signature. They have ironed out the kinks in the virus.
While multiple options for a Corona vaccine are on the table, 70 versions at last count, only a small handful will make the grade. One candidate Barouche, a subsidiary of pharmaceutical giant Johnson & Johnson, is employing simian-derived adenoviral vectors, genetically engineered “in just four weeks” to propagate the virus for mass production. ‘On March 30 the U.S. and Johnson & Johnson committed more than $1 billion to fund large human clinical trials, which are slated to begin in September if the limited testing proves out.’ Anyone who gets this product will potentially be exposed to simian immunodeficiency virus (SIV), the monkey derived version of HIV Aids. ‘Some experts also worry an adenovirus itself could replicate inside the body and cause disease.‘ It would be a mistake to assume the virus is predictable. Covid-19 is airborne and insidious, and has demonstrated a propensity for horizontal spread unlike anything before, because it was structurally engineered to survive adversity.
‘The immunological objective of the current prophylactic vaccine candidates is to induce neutralizing antibodies that inhibit the CoV entry to the cells. The goal is to vaccinate approximately 60% of the population and to reach herd immunity against COVID-19. SARS-CoV-2 is not a highly mutagenic virus because it carries proof-reading machinery, like other CoVs. Its relatively stable genome represents an advantage for vaccine development compared to highly mutating viruses like HIV-1.‘ In fact, the virus does contain HIV, and therefore it will mutate.
The virus identified as Covid-19 was conceived in a laboratory in 2015, a chimeric hybrid of SARS Corona, interwoven with human HIV Aids. The addition of a simian immunodeficiency viral component sharply increases the likelihood of hybrid cancer, auto-immune dysfunction leading to pneumonia and premature death in the newly vaccinated host. ‘Three European biotech companies agreed to collaborate on the development and large-scale manufacture of a novel adenoviral vector-based vaccine against COVID-19. The vaccine candidate is expected to enter clinical trials during summer 2020 with large-scale vaccine production planned to start soon after…The vaccine technology is based on a ReiThera proprietary simian adenoviral vector with strong immunological potency and low pre-existing immunity in humans, explains Stefano Colloca, chief technology officer. Vaccines based on simian adenoviral vectors have been evaluated in Phase I and II clinical trials and proved to be safe and immunogenic, he adds. ReiThera is preparing for a COVID-19 first-in-human trial to be started in Italy in summer 2020.’ In simian virology, SAdV-7, intrinsic to adenovirus cross infection, refers to “simian adenovirus SV-25” in the M. mulatta or Rhesus macaque population.
- ‘In SIV/HIV infection, a critical preferential loss of Th17 memory cells is observed and this has been associated with a loss of mucosal barrier integrity, bacterial translocation and infection…Ulcerative colitis (UC) and Crohn’s disease (CD) represent the two major forms of IBD and both are generally believed to be driven by aberrant T-cell responses to the intestinal flora…There are at present three established subsets of effector CD4 T cells – Th1, Th2 and Th17 – each of which are suggested to play a role in one or another variant of IBD. In addition to CD4 T cells, auto-aggressive CD8 T cells in the gut have also been implicated in the progression of IBD. Naive CD8 T cells have also been shown to be able to induce colitis in an IL-17-dependent fashion…Although both adaptive and innate immune responses are thought to initiate and propagate the inflammation, CD4 T cells have been shown to play a central role in celiac disease pathogenesis.‘
- ‘There was a significant correlation between cellular density and mucosal CD3+ lymphocytes, and between mucosal CD3+ and CDS4+ lymphocytes. Although mucosal CD4+, CD45RO+ ‘memory” cells were decreased, CD8, CD45RO+ ‘memory’ cells were increased. Mucosal CD4+ lymphocyte depletion occurred early in HIV, and thus their role in mucosal protection against opportunistic infection should be revised. Mucosal CD8+ lymphocytes initially increased, but decreased when CD4 blood counts were depicted, perhaps contributing to loss of host protection against infection. Intraepithelial lymphocyte depletion may also contribute lo opportunistic infection.‘
- ‘New evidence suggests that mucosal CD4 TRM populations differentiate at tissue sites following the recruitment of effector T cells by local inflammation or infection. The resulting TRM (Tissue-resident memory T cells) populations are enriched in T-cell specificities associated with the inducing pathogen/antigen.’
- ‘The mucosal immune system plays a central role in both the transmission of HIV infection and the pathogenesis of AIDS. Most HIV infections are acquired through mucosal transmission, and quantitative and qualitative defects of mucosal immunity are consistently present in all stages of pathogenic HIV and SIV infections. A series of recent studies has emphasized the role of a rapid, dramatic, and largely irreversible depletion of mucosa-associated lymphoid tissue-based memory CD4(+)CCR5(+) T-cells as a key determinant of disease progression in HIV-infected individuals and SIV-infected macaques…Importantly, the mucosal immune dysfunction observed during pathogenic HIV and SIV infection is associated with translocation of microbial products (i.e. lipopolysaccharide) from the intestinal lumen to the systemic circulation where they may be responsible, at least in part, for the chronic immune activation that follows pathogenic HIV and SIV infections.‘
- ‘For adenovirus, which naturally infects mucosal surfaces, the maintenance of its replicative capacity is preferential and well suited for HIV vaccine strategies, but also may risk establishing persistence and potential vaccine transmission…Picker et al. has recently found that half of the macaques vaccinated with a cytomegalovirus (CMV) derived vector encoding SIV genes were able to suppress viral load to undetectable levels after repeated rectal SIV challenge…CMV is a pathogen as well, and currently even has vaccine strategies geared towards it. While it is generally nonpathogenic in humans, those who are pregnant or immunocompromised may still be exhibit a significant risk.’
- ‘To gain insight into the basis of this difference, we established a recombinant adenovirus system expressing the S protein from SL-CoV (rAd-Rp3-S) to investigate its immune characterization.‘
Prolonged exposure to viruses like Corona actually benefits the capacity of the immune system to adapt. We’re not meant to be hermetically sealed organisms, but that is ultimately where the medical establishment is leaving us. Due to incarceration and self-isolation policy we are rendered more susceptible to long-term infections, accelerated neuro-degeneration and prone to diseases we might otherwise skirt altogether. No matter how daunting the task may seem, the only way to build antibodies to Covid-19, for our bodies to learn and adapt to it, is through natural environmental exposure to the strain – regardless of the risk factor, albeit it is sensible to shelter those in the community with acutely fragile immunity and pre-existing medical conditions, often resulting from vaccine-injury and prescription drug-dependency. Epidemiologists and virologists are well aware of this knowledge, but have either been sworn to silence, and intimidated by medical authorities such as the AMA, on fear of being ostracized, censored for speaking out or demoted in their department or else they lack the fortitude to take a stand. In this climate of authoritarianism no one is safe to indulge in independent scientific inquiry, for fear of losing their employment and status.
The new Corona vaccine produced by GlaxoSmithKline and Sanifo will be made using insect viral vectors, which have been linked to immune system disorders and microbial related gut issues from contaminated larvae. The adjuvant used is GSK’s proprietary squalene formula, a synthetic derived form of squalene which has been linked to gulf-war syndrome in troops who were given the squalene-based Anthrax vaccine. Squalene is found throughout the human body. It acts as the lubricant in our joints.
In the context of a toxic viral vaccine such as Covid-19, squalene is being injected into the body intramuscularly alongside recombinant viruses laced with baculoviruses and harmful excipients in this case. The contents enter the bloodstream, whereupon the immune system cannot distinguish between the synthetic mimic and naturally occurring deposits of squalene, and to defend itself systematically begins to attack its own supply of squalene everywhere, leading to a host of neuro-degenerative problems, widespread auto-immune breakdown, triggering early onset Arthritis in children.
This orchestrated Pandemic will have far-reaching implications for families. As we are thrust by forces outside our control, to follow instructions altering our life completely, everything is upside down. The way in which we think and the freedom we expect to live in society is being broken down and re-engineered. We are led to believe the narrative as truth, and the sacrifices families have made are seen as necessary. Never in history has media been used so efficiently, and such a powerful instrument of control and persuasion is seeping into the hearts and minds of ordinary people, changing the way in which humans interact. Our children are the most at risk for permanent fracturing, and the infusion of fear with protecting your loved ones, an instinct which all children share, the impulse to protect our loved ones, has been inverted, and children will equate self-sacrifice and blind obedience to the government as normal. The new normal is going to mean children whose natural instinct is to trust their parents, will be forever caught in a tunnel, from trauma and propaganda.
The government is supplanting the role of caretaker, and children will grow up without any internal compass for independent judgement, having grown up institutionalized to turn to government for guidance and answers. Parents know in their gut and their bones and blood that this something about this crisis is terribly wrong. It is incumbent upon parents to break through the hall of mirrors and take back the power that has been stolen from them. Children are not aware of the meaning and implications of a medical dictatorship, only the role they have in navigating the chaos day to day from their vantage point. The time will come when every tenet of health freedom is rewritten by those in control of the populace, to suit their frightening agenda. Children do not deserve to be thrust into the eye of this storm, but they will grow up in a world where scientific inquiry is a sham, where schools are used to train the young to distrust natural immunity, by separating them and dictating their social behavior with devices better suited for a prison. The only way we can reclaim our families and live in this new model of the world, is to break that mold and rebuild the world back into what it was meant to be, based on the noble ideas of life, liberty and the pursuit of freedom.
No one actually dies from the flu. Those who succumb to Influenza die from bacterial pneumonia triggered by flu-like symptoms. That is a scientific fact. Similarly, contrary to mainstream media misinformation, no one actually dies from Covid-19. That is a fallacy. Instead, they are dying from a multitude of comorbidities, pre-existing medical conditions and excessively compromised immunity. The chief culprits leading to Corona fatalities are diabetes, heart disease, arrhythmia, hypertension, obesity, cancer, liver and kidney failure, just exacerbated by the virus. In many instances the individual may have already been on the verge of dying previous to acquiring the Corona infection, and some simply did not recognize early warning signs. Others have chronic health issues affecting respiratory health, either heavy smokers or working in a toxic breathing environment. That is not meant to be construed as a generality or a superficial analysis of these cases.
There is so much more going on here than a mere virus. The ventilators are triggering heart attacks, and also generating ventilator associated pneumonia, the sedatives used in conjunction to facilitate running the feed the tube down into the trachea is another serious factor. Corona patients put on ventilators are given sedatives which can can trigger irregularities of the heartbeat, arrhythmia leading to induced cardiac arrest. The intubation and extubation procedure, the insertion and removal of the breathing apparatus into the trachea is extremely invasive. Many of these cases in patients with heart problems being categorized as a Corona precipitated death on the Death certificate, are inaccurate. In NY, where 80% of patients placed on ventilators have died, those instances involving cardiac complications in ICU, the sedative had spurred a sudden heart attack and terminated the patient’s life. Sedatives in use include Propofol, Midazolam and Dexmedetomidine, all of which are linked to arrhythmia. Chloroquine is causing heart failure and respiratory distress leading to death. The virus is laced with an HIV component which is also breaking down and handcuffing the immune system from fighting off the infection. The use of anti-viral AIDS treatment to quell symptoms is killing patients. The list is long and complicated. But this notion that these are all strictly Covid-19 deaths is ludicrous. Coronavirus itself does not kill anyone, and death certificates should respect that, instead of spreading fear and false data to push their agenda. Families deserve to know the truth.
The agenda behind this overblown crisis is clearly to establish a medical dictatorship. While communities languish in their homes, pummeled 24/7 with falsified statistics equating the battle against Covid-19 with World War 2, the foundation of health freedom is being razed and bulldozed into the ground by the WHO and its minion bodies throughout the medical establishment. Final preparations are underway to secure society for conditions of the new normal. Social distancing and mandatory vaccination are to become a permanent fixture in the world now, and the Corona virus will be used as a lever to bring down the holistic health movement and enforce measures against families embracing vaccine hesitancy. Major vaccine corporations are lining up at the gates in preparation for the roll-out of the Corona vaccine. We are living under an oppressive dictatorship when critical thinking is brandished as a form of terrorism, and those in positions of authority rank as judge and jury over us, and health freedom is locked away, when our voices are silenced forever, drowned out by the moral majority that believes the message of its captors, and alienates those who challenge the status quo. We have reached the point where the institutions of healthcare to which we have invested our trust as families have run afoul and are using that power against us. For that betrayal they must be held accountable.The moral majority, soon to be freed from the shackles of self-isolation now represents the singular most dangerous threat standing in the way of independent health freedom, far greater even than that the WHO.
This report is ultimately intended, not as an indictment of government wrong-doings, so much as a vehicle for discussion on these matters of great importance to humanity. It is my hope that we continue on the path to ending medical corruption and that the truth uncovered in this dossier is met with a proper response by the people, who in turn apply relentless pressure upon their elected government around the world, in pursuit of more noble tenets of social justice and ethics. The case is not closed, and this health crisis is still unfolding. Justice will only be served when we have routed the seat of corruption.