During a Senate hearing on the COVID-19 pandemic response, Senator Rand Paul, a physician and politician from Kentucky alleged that the National Institute of Health (NIH) had been funding the Wuhan lab in China. Dr. Paul claimed they “juiced up” a virus that was originally found in bats to create a super virus that can infect human cells. This virus then somehow escaped, either because of an accident or because it was deliberately released.
Senator Paul was literally accusing Dr. Anthony Fauci of funding and overseeing “Gain-of-Function” experiments in cooperation with the Chinese government that produced SARS-CoV-2.
Fauci noted that although the NIH did fund a project at the Wuhan lab, it was not meant for “Gain-of-Function” research into human-made super viruses; the NIH gave a grant to a group called Eco Health Alliance, which hired the virology lab in Wuhan to conduct genetic analyses of bat coronaviruses and examine how they spread to humans.
Gain-of-function research is a controversial form of study that involves boosting the infectivity and lethality of a pathogen. Fauci has advocated for the research in the past, but he denied that the NIH was funding it in China. But Paul interrupted him and hinted that not only was the virus introduced to the world because of a lab accident, it was also biologically engineered. “Government scientists like yourself who favor gain of function … ” Paul said.
Even though Fauci continued to say that he did not support “Gain-of-Function” research in China—these risky experiments have often been conducted in various WHO-supervised BSL-4 laboratories around the globe specifically at Fort Detrick under Fauci’s direction and with the co-operation of Chinese Scientists having direct ties to the Chinese Military! In fact, an aerosol form of the Ebola virus exists today because of these “Gain-of-Functions” experimentations!
In the following article’s Civilian Intelligence Network laid out how the Winnipeg National Lab in Canada, Fort Detrick in the USA and the Wuhan lab worked together to bring about this Pandemic. This connects Fauci, Dr. Tam and Dr. Xiangguo Qiu, the Chinese Scientist escorted out of the NML in Winnipeg with direct ties to the Chinese Military! There was no spying or stealing, and it was all administered by the WHO!
Backstory: On May 4th 2013 a deadly SARS-like virus called the MERS virus that causes Middle Eastern Respiratory Syndrome, was sent to the Canadian National Microbiology Lab in Winnipeg. The MERS virus was initially isolated in Saudi arabia and sent to Erasmus Medical Centre in Rotterdam, the Netherlands. So why transfer a deadly virus to Canada? At the time, sovereign laws in the Netherlands would not allow China direct access to potential bioweapons. Canada was chosen because it was known for housing some of the worlds most deadly pathogens.
“The National Microbiology Laboratory in Winnipeg is working with a sample of the new coronavirus that’s causing clusters of infections abroad — but can’t share the material with other researchers across the country despite the public health urgency. But before they could start, officials had to sign a material transfer agreement, a contract that outlines the terms and conditions for using the coronavirus sample.”
“Such agreements exist for different reasons — sometimes because countries want to make sure a dangerous bug won’t fall into the wrong hands, sometimes because they want to exert their rights if a vaccine or treatment is developed. But the agreements also impede the research process, say scientists.”
“We can’t distribute [the virus] any further, which is a problem, because a lot of people would like to be working on this and can’t,” Plummer said.”
fig 1 https://www.cbc.ca/news/health/saudi-coronavirus-work-stymied-at-canadian-lab-1.1322426
fig 2 https://www.ctvnews.ca/health/health-headlines/canada-s-national-lab-has-sample-of-new-coronavirus-1.1281929
The story does not end there. Since 2006, Canada also collaborated with Chinese scientists working directly for the Chinese Military and up until 2021 the Canadian taxpayer even paid them a salary! Eventually this MERS virus, along with Ebola and Marburg would end up in the hands of the Chinese. No spying. No stealing. It was all administered by covert agents of the WHO residing within the Public Health Agency of Canada (PHAC). Canada was but a broker who assisted with the transfer.
Brain stem injury is indicated in MERS and SARS and they have implicated it for SARS-CoV-2 as well… through the olfactory bulb! (This is also the location where they do the nasal swabs).
fig 2.5 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192347/
How was this MERS transfer organized? The initial WHO meeting of all stakeholders too place in February of 2013 and consisted of the following consultants which included Dr. Theresa Tam of the PHAC (Public Health Agency of Canada), the CDC, the ECDC (European Center for Disease Control), members from the Robert Koch Institute, Germany, France and the Erasmus Medical Center in the Netherlands who had the MERS virus. This WHO working group of consisted of representatives from the main allied countries.
fig 3 http://web.archive.org/web/20130323024855/https://www.ecdc.europa.eu/en/publications/publications/novel-coronavirus-rapid-risk-assessment-update.pdf
Why is this significant? in 2003 there was a global outbreak of the coronavirus SARS-CoV-1 where approximately 8,098 people got infected and developed SARS (Severe Acute Respiratory Syndrome), of these 774 died. The MERS virus was discovered in 2012 in Saudi Arabia and is also a coronavirus. However the MERS virus is far more infectious and carries a higher mortality rate than the SARS virus, especially in the elderly and in those with co-morbidity.
Does this sound familiar? Furthermore, MERS is an aerosol which means it’s easily transmissible via airborne droplets!
Since both are known to be human pathogens, there are many people in the scientific community that believe “Gain-of-Function” experiments were done to create a weaponized version of these virus… SARS-CoV-2!
SARS + MERS(airborne) = SARS-CoV-2
fig 4 https://academic.oup.com/cid/article/63/3/363/2595016
When the MERS virus was initially sent to the Erasmus Medical Center in the Netherlands, Erasmus submitted a patent application dated September 23, 2013 for the MERS virus to the European Patent Office. This gave them oversite as to the distribution of any and all genetic material and vaccines that could be developed from this MERS virus.
fig 5 https://data.epo.org/gpi/EP2898067B1-HUMAN-BETACORONAVIRUS-LINEAGE-C-AND-IDENTIFICATION-OF-N-TERMINAL-DIPEPTIDYL-PEPTIDASE-AS-ITS-VIRUS-RECEPTOR
Now a confidential agreement between Fauci’s NIH and Moderna, dated November 9, 2015 has surfaced showing that Fauci’s NIAID had transferred MERS genetic material to Moderna and “it’s affiliates” which was considered priporitory information and was redacted in the disclosure document (bottom figure marked in yellow). Who were the “affiliates” working with Moderna on the deadly MERS pathogen?
fig 6 & 7 https://s3.documentcloud.org/documents/6935295/NIH-Moderna-Confidential-Agreements.pdf
fig 8 https://www.documentcloud.org/documents/6935295-NIH-Moderna-Confidential-Agreements.html
Fig 9 https://f.hubspotusercontent10.net/hubfs/8079569/The%20FauciCOVID-19%20Dossier.pdf
These are very dangerous pathogens that are heavily guarded and if placed in the wrong hands could lead to acts of biological terrorism. How did Fort Detrick receive the MERS virus? Why was a government lab providing deadly pathogenic material to a Pharmaceutical company? Were there other confidential agreements signed? where their “Gain-of-Function” experiments were being conducted at Fort Detrick? Was Moderna doing experimentation with MERS? Who were these “affiliates” working with Moderna and who else was in the loop?
Basically there was no oversight what-so-ever. What we do know is that the Canadian lab and Chinese scientists were working on an Ebola vaccine at Fort Detrick since 2006; the very same Chinese scientists who were collaborating directly with the Chinese military and sending them deadly pathogens. In fact, there were email exchanges from Chinese affiliates that confirm this!
“We would like to express our sincere gratitude to you all for your continuous support, especially Dr. Qiu and Anders! (Anders was a technician at the NML) Thanks a lot!! Looking forward to our further cooperation in the future,” said the heavily redacted email, which does not provide the name of the sender.”
fig 10 https://www.cbc.ca/news/canada/manitoba/canadian-scientist-sent-deadly-viruses-to-wuhan-lab-months-before-rcmp-asked-to-investigate-1.5609582
fig 11 https://thebulletin.org/2014/08/making-viruses-in-the-lab-deadlier-and-more-able-to-spread-an-accident-waiting-to-happen/
Fig 12 https://twitter.com/XHNews/status/1418873125706547201
Plot Twist: Here are Moderna’s Affiliates! In the Chinese Newspaper, Global Times (dated February 2, 2021) titled, “Chinese Scientist’s Research boosts Pfitzer and Moderna COVID-19 Vaccine Development,” they report on the laboratory research of Dr. Xinquan Wang, a professor with the Chinese Academy of Science which reports directly to the Chinese Military. His research student, Wang Nianshuang was acknowledged for his work on the MERS virus in 2013!
How did China get the pathogen when it was supposedly tucked away in Canada’s BSL-4 lab under tight security? Not only that, the article states that China now has the antiserum for treatment of MERS infections!
“Wang started working on coronaviruses in 2013 when he was a PhD student in Xinquan Wang’s lab. He determined the structural mechanism of MERS-CoV receptor recognition. Then partnered with another professor at Tsinghua’s medical school Zhang Linqi in 2014, Wang and colleagues discovered the first human monoclonal antibody that can strongly neutralize the coronavirus that causes Middle East Respiratory Syndrome (MERS).”
Fig 13 https://www.globaltimes.cn/page/202102/1214667.shtml
And guess what? Moderna’s CEO Stephane Bancel filed a patent on the MERS active site or “spike protein” on March 4, 2016 called “Modified Polynucleotides for the Production of Proteins Associated with Human Disease” or in layman’s terms: Viral mRNA that will be used to make “spike proteins”.
Fig 14 https://patentimages.storage.googleapis.com/de/f4/cb/51779d7ad7b8a6/US20160199513A1.pdf
Just what exactly is Moderna’s Scientist Wang’s claim-to-fame? Wang and colleagues published the first structure for the Sars-CoV-2 virus spike protein in the journal Science in March 30, 2020.
They shared the viral mRNA “computer model” with more than 100 labs and also participated in vaccine development in cooperation with vaccine manufacturers such as Moderna. You see… China always had MERS. They all had MERS, SARS and HIV… and they all participated in “Gain-of-Function” experiments to appease their NWO masters!
fig 15 https://www.nature.com/articles/s41586-020-2180-5
fig 16 https://life.tsinghua.edu.cn/lifeen/info/1033/1091.htm
Furthermore, Moderna’s CEO Stephane Bancel just recently stated on a World Economic Forum (WEF) zoom conference that Moderna took just 2 days to design the vaccine on the computer. Why? Moderna was already working with Fauci’s team for two years on the MERS coronavirus (According to the confidential agreement the collaboration was going on since 2015). They already knew that the “spike protein” was the active site! Coincidence or confirmation that the pandemic was predetermined and preplanned?
Now Here’s the Fuckin Insane Plot Twist: Yes, just when we thought we saw the last of these “mind blowing” revelations on the SARS-CoV-2 Story and its evolution, we now have the Rothschilds throw a wrench into the works! A patent was filed by Rothschild on October 13 2015, before the confidential agreement with Moderna on a testing protocol for COVID-19 that would require the use of cell phones to test for the presence of the virus in a persons body:
fig 17 https://pubchem.ncbi.nlm.nih.gov/patent/US-2020279585-A1
Rothschild also holds the Biometrics Patent which means Big Brother is already here! They are monitoring all those vaccinated to determine location, activity, behavioural… everything! Say hello to your new Daddy! Daddy SEE everything and Daddy HEAR everything!
Fig 18 & 19 https://patents.google.com/patent/US10242713B2/en
What does this all mean? Here’s a timeline to help you:
- February 12 2013: WHO meeting of Stakeholders which included Erasmus Medical Center of the Netherlands, Dr. Theresa Tam of the PHAC (Public Health Agency of Canada), the CDC, the ECDC (European Center for Disease Control), members from the Robert Koch Institute, Germany, France.
- May 4 2013: Canada’s NML receives the MERS virus from the Erasmus Medical Center in the Netherlands.
- September 23 2013: Erasmus Medical center in the Netherlands files a Patent on the MERS coronavirus.
- China 2013: Here are the Chinese “affiliates” working with Moderna: Wang Nianshuang started working on coronaviruses in 2013 at the Chinese Academy of Science which reports directly to the Chinese Military. He determined the structural mechanism of MERS-CoV receptor recognition, then partnered with another professor at Tsinghua’s medical school in 2014, Wang and colleagues discovered the first human monoclonal antibody that can strongly neutralize the coronavirus that causes Middle East Respiratory Syndrome (MERS). Basically it means the Chinese have the cure for MERS!
- November 6 2015: NIAID, Moderna & “affiliates” sign Confidential Agreement transferring MERS genetic material from Fort Detrick to Moderna & Affiliates.
- July 4 2016: Moderna files an mRNA patent on the MERS virus active site or “spike protein.” Since “MERS” is not specifically identified in the patent we believe this patent (which was an extension to the Erasmus MERS patent) is indeed the SARS-CoV-2 weaponized mRNA sequence for the spike protein in vaccines.
- March 30 2020: Wang and colleagues published the first structure for the Sars-CoV-2 virus spike protein. They shared the viral mRNA “computer model” with more than 100 labs and also participated in vaccine development in cooperation with vaccine manufacturers such as Moderna.
However with Rothschild filing a COVID-19 testing patent on October 13, 2015 it means that the SARS-CoV-2 virus was already weaponized, that the “spike protein” or active region was isolated, and the viral mRNA sequence was already deciphered! It also means that the majority of this work was carried out in collaboration between Fort Detrick and China at the Chinese Academy of Science which worked directly with the Chinese Military!
Exactly what did Fauci’s NIAID give Moderna & Affiliates in that “Confidential Agreement”? Our guess is… the mRNA sequence to the weaponized SARS-CoV-2 spike protein sequence used in the COVID-19 vaccines! The very same sequence that contains SARS+MERS+HIV. It was already weaponized before they gave it to Moderna who then transferred it to its “Affiliates” in China where they could conduct “Human Trials” (most likely on inmates in Chinese prisons). This was in 2016, so it is highly probable that they know the long-term outcomes of the viral mRNA vaccines already!
Where were the Gain-of-Function” experiments done? Initially we assumed that all BSL-4 labs had both the SARS and the HIV-1 virus and were capable of “Gain-of-Function” experiments. However, a group out of France determined that France’s Pasteur Institute was responsible for weaponizing SARS-CoV-1(caused the SARS outbreak in 2003) and HIV-1. Their only fault was in not recognizing the importance of the MERS coronavirus.
Instead they speculated that it was a “Malaria Genome” that was inserted that caused the SARS-CoV-2 virus to become airborne. This in turn escalated the Hydroxychloroquine (HCQ) frenzy on social media as a potential cure for COVID-19 despite the fact that HCQ suppresses the immune system in COVID-19 infected patients! A narrative that was supported by French Nobel laureate and NWO “Controlled Opposition”, Dr. Luc Montagnier. If you recall, the original India study released in January 2020, established that there were 4 HIV-1 inserts in the active region or “spike protein” of the COVID-19 virus also stated that the COVID-19 virus closely resembled both SARS and MERS in functionality and in the phylogenic tree.
fig 20 http://d.p.h.free.fr/covid19/docs/TRUTH_about_Covid-19_and_Covid-19_Vaccines.pdf
fig 21 https://www.biorxiv.org/content/10.1101/2020.12.12.422516v1.full
With respect to weaponizing the MERS virus component of the SARS-CoV-2 virus, most of those experiments were more than likely conducted by the NIAID at it’s Fort Detrick‘s laboratory who then gave what was identified as “MERS” genetic material to Moderna & Affilates. We believe NIAIDs Fort Detrick weaponized the SARS-CoV-2 virus itself and included all 3 viral components (SARS-CoV-1, MERS, HIV-1) within the viral genetic material that they handed over to Moderna & Affiliates in order to develop their toxic mRNA vaccine and conduct secret human trials in China.
Fort Detrick is “COVID-19 Central” and China is Rothschild’s “Headquarters!” Furthermore, since the weaponizing required the MERS virus itself, we believe that the allied nations involved in the original WHO-MERS working group were all complicit in weaponizing what we know as the SARS-CoV-2 virus! Our own governments are intentionally trying to kill us!
Just how deadly is the MERS virus? MERS carries a mortality rate of 35% and if the vaccines have been weaponized you can expect 1 in 3 people succumbing to these vaccines. They are now reporting that “future variants” may kill 1 in 3 people. Who has the MERS vaccine? Why Moderna’s Affiliates do… in China! (Timeline: 2013 above) The real question is: What part of the SARS-CoV-2 virus or vaccine will kill you first? Will it be the fast kill associated with MERS at 35% or the slow kill over a period of 3 years due to HIV? Regardless, the majority of the population will be dead within 3 year!
fig 22 https://www.dailymail.co.uk/news/article-9844701/SAGE-Covid-variant-kill-one-three-people.html
Proof HIV inserts are in Sars-Cov-2:
But the SARS-CoV-2 story does not end yet. When the SARS-CoV-2 pandemic started, there was a small research group from the Indian Research of Technology, in New Delhi, who shocked the world and the scientific community with their revelations that there were 4 HIV inserts in the SARS-CoV-2 virus.
Everyone, including CIN automatically came to the conclusion that the SARS-CoV-2 virus was a bioweapon and was helping to transmit AIDS-like disease on mankind. Some even went as far as calling it “Airborne AIDS” owing to the fact that it was a respiratory virus. Unfortunately… we weren’t too far off track! Through “Gain-of-Function” manipulations we now have a weaponized virus that can attack the immune system!
Plot Twist: HIV is a very unique virus in that it is sensitive to electromagnetic radiofrequencies which trigger or activate binding sites on the virus. This is how 5G along with Graphene oxide fits into the picture; graphene oxide is electromagnetic and acts like a receiver or antennae for 5G. Both are required to activate the vaccine within the body with 5G levels controlled by the NWO! 5G is said to be fully activated by August 2021… at the start of the 4th wave! Research that CIN conducted independently shows that the 5G frequency are already set at kill frequency range, and the effects of which are cumulative!
SARS + MERS (airborne) + HIV (immune system & 5G) = SARS-CoV-2
fig 23 https://hal.archives-ouvertes.fr/hal-01113827v2/document
This Indian article, published on January 31 2020, confirms that the SARS-CoV-2 contained unique “spike protein” that were not present in other coronavirus. In addition, the amino acid residues in all the 4 spike protein inserts were similar to those in the HIV-1 Glycoprotein 120 (GP120) or HIV-1 Gag (Group specific antigen for HIV); the antigen that launches an attack against the immune system in those that are infected with the HIV causing AIDS. The study concluded that it was unlikely for a virus to have acquired such unique insertions naturally in a short duration of time leading everyone to surmise that SARS-CoV-2 was a bioweapon.
fig 24 https://www.biorxiv.org/content/10.1101/2020.12.12.422516v1
fig 25 https://www.cell.com/trends/microbiology/pdf/S0966-842X(12)00212-0.pdf
After they published the results of the study, it attracted heavy criticism from social media experts that the authors were forced to retract their paper. At the time, French Nobel prize winner Dr. Luc Montagnier agreed with the findings of the study stating:
fig 26 https://twitter.com/AubeDigitale/status/1251152579498668035
SARS-CoV-2 Virus Similar to HIV!
Recent research confirms Dr. Luc Montagnier’s statement that SARS-CoV-2 is a disease that attacks the human immune system similar to the HIV-1 virus. Several studies are now showing that SARS-CoV-2 creates an autoimmune dysfunction within the body.
fig 27 https://www.nature.com/articles/s41584-020-0448-7
The pathophysiology of severe COVID-19 disease been attributed to a hyper-inflammatory response without a clear indication of the underlying mechanism. There is a characteristic delay in the onset of respiratory distress, approximately 6 to 12 days after the start of symptoms, which is not typical for a severe viral respiratory infection. Furthermore, viral cultures of SARS-CoV-2, beyond day 9 of illness, are negative for the virus.
So what is causing the delayed disease onset? The timing of respiratory distress due to COVID-19 coincides with the onset of the humoral immune response, and there is evidence of elevated autoantibodies, antibodies that attack the body itself, among hospitalized COVID-19 patients that include:
- Elevated Anti-interferon Antibodies: Interferons are a group of cell-signaling proteins made and released by body cells in response to the presence of a virus; cells communicate with one another using signaling proteins… like a “chat-line.” Virus-infected cell will release interferons causing nearby cells to heighten their anti-viral defenses. High levels of “Anti-interferons Antibodies” suggest that the immune system is attacking these interferons that would otherwise tell healthy cells that there is a viral infection. Elevated Anti-interferon antibodies can also be found in HIV infected Persons.
fig 28 https://pubmed.ncbi.nlm.nih.gov/2500007/
- Elevated Antiphospholipid Antibodies: People who have one or more Antiphospholipid antibodies and those that are diagnosed with Antiphospholipid Syndrome can have an increased risk of having recurrent blood clots, recurrent miscarriages, and/or low platelets (thrombocytopenia). Antiphospholipid antibodies have been detected in patients with HIV disease.
fig 29 https://pubmed.ncbi.nlm.nih.gov/7597491/
Both Lupus anticoagulant (LAC) and anticardiolipin antibody (aCL) (these are sub-types of antiphospholipid) were found on SARS-CoV-2 patients. Similar findings are presented with HIV infected patients.
fig 30 https://onlinelibrary.wiley.com/doi/10.1002/art.41472
fig 31 https://pubmed.ncbi.nlm.nih.gov/9184392/
- Elevated levels of Extrafollicular B-cell activation: Extrafollicular B-cell activation refers to the activation of cells of the immune system which normally correlates with elevated antibody production to neutralize infecting pathogens (i.e. virus, bacteria). Yet, in SARS-CoV-2 patients despite elevated immune system B-cells they presented with severe disease, elevated inflammatory biomarkers, multiorgan failure and death. These findings strongly suggest that the immune system itself is attacking the body in COVID-19 disease similar to what occurs with HIV infection.
fig 32 https://www.nature.com/articles/s41590-020-00814-z
fig 33 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5300048/
- Elevated Anti-Annexin-A2 Antibodies: Annexin-A2 is a calcium-dependent phospholipid-binding protein that plays a role in the regulation of cellular growth and cell signaling pathways. Annexin A2 has been proposed to function outside the cell in anticoagulant reactions. Elevated antibodies against Annexin-A2 have been shown to cause lung fibrosis and clotting in COVID patients. In HIV infection, Annexin-A2 protein binds to HIV-1 and helps with viral replication.
fig 34 https://pubmed.ncbi.nlm.nih.gov/16501079/
This type of immune response is characteristic of several autoimmune diseases, specifically AIDS. Was the SARS-CoV-2 virus altered using “Gain of Function” genetic manipulation as predicted by Dr. Luc Montagnier? And if so, is the SARS-CoV-2 virus HIV-like?
fig 35 https://erj.ersjournals.com/content/early/2021/07/01/13993003.00918-2021
Human immunodeficiency virus (HIV) integrates into the host genome or DNA. As such, an HIV-infected individual is infected for life. Does the same thing happen with SARS-CoV-2 infection? CIN recently published an article on a postmortem examination of a vaccinated patient which showed viral RNA in almost all organs examined.
Vaccine manufacturers, Governments, Medical authorities and Media have informed us that the mRNA in the vaccine is destroyed within the cell after it codes for “Spike Proteins”. Why then is viral RNA still there and why was it in every single organ despite being told it would target the immune system only? Would one expect to see the SARS-Cov-2 virus inside cells as well?
A recent study published on May 25 2021, confirms our worst fear; SARS-CoV-2 RNAs can be reverse-transcribed and integrated into the DNA of human cells. What’s worse is that these viral sequences can then be transcribed from the integrated DNA sequence which then accounts for the detection of viral RNA by PCR in patients after infection and clinical recovery. But is the SARS-CoV-2 virus still there?
fig 36 https://www.pnas.org/content/118/21/e2105968118
Viral latency is the ability of a pathogenic virus to lie dormant (latent) within a cell. Like the HIV virus, SARS-CoV-2 virus can also remain dormant; South Korean officials reporting that nearly 100 people thought to be cured of the novel coronavirus tested positive for COVID-19 again. They believe the virus may have “reactivated” in the patients rather than them becoming re-infected.
fig 37 https://www.thehindu.com/sci-tech/health/the-hindu-explains-is-sars-cov-2-a-latent-virus-which-can-recur/article32192853.ece
What does this mean? Basically, like HIV, the SARS-CoV-2 infection is there for life! It’s not surprising that Fauci wanted the Indian study to be discredited! He had to fulfil his NWO agenda first; implement the vaccine rollout and infect as many people as possible!
Are Vaccinated People Contagious?
Recently, there has been speculation regarding the safety of COVID-19 mRNA vaccines and the potential nightmare that will unfold in a matter of weeks. The viral mRNA vaccines, regardless if they’ve been delivered using lipid nanoparticles (Pfizer, Moderna) or by using an adenovirus shuttle (AstraZeneca, J&J), spread throughout the body, the resulting production of the vaccine antigen or ‘Spike protein” will both stimulate immunity and also cause those same cells to be attacked by the immune system. Studies have shown that this can happen with live virus but If this actually happens with the vaccines, the resulting symptomology could resemble clinical symptoms seen with autoimmune diseases such as advanced HIV disease or AIDS.
Why are serious health issues now emerging from vaccinated individuals? You see… it was recently revealed in a Texas Senate Committee hearing that COVID-19 vaccine trials in animals were stopped because they kept on dying! None of the vaccine manufacturers finished animal studies nor did they conduct long-term outcome studies normally done BEFORE a drug is brought to market. Here is the Senate Committee hearing on May 6, 2021 with testimony from Dr. Angelina Farella:
“And from what I’ve read, they actually started the animal tests and because the animals were dying, they stopped the tests…. Folks, I think that’s important to understand there that what we’re talking about is American people are now the guinea pigs. This is the test program, that’s going on.”
The Founder of Children’s Health Defense states:
“Scientists first attempted to develop coronavirus vaccines after China’s 2002 SARS-CoV outbreak. Teams of US & foreign scientists vaccinated animals with the four most promising vaccines. At first, the experiment seemed successful as all the animals developed a robust antibody response to coronavirus. However, when the scientists exposed the vaccinated animals to the wild virus, the results were horrifying. Vaccinated animals suffered hyperimmune responses including inflammation throughout their bodies, especially in their lungs.”
This article in the Global Research archive which has been deleted from the internet states:
“COVID-19, like other coronaviruses, is expected to mutate at least every season, raising serious questions about claims that any vaccine will work. A successful vaccine has never been developed for any of the many strains of coronaviruses despite 30 years of effort, due to the nature of the virus itself. In fact vaccinated people can have a higher chance of serious illness and death when later exposed to another strain of the virus, a phenomenon known as “virus interference.” An earlier SARS vaccine touted as effective because it produced antibodies to the virus never made it to market because the laboratory animals contracted more serious symptoms on re-infection, and most of them died.”
Scientists are now finding that vaccinated people have a higher risk of infection compared to unvaccinated proving that the vaccine itself acts to suppress natural immunity. “Israelis who were vaccinated were 6.72 times more likely to get infected after the shot than after natural infection, with over 3,000 of the 5,193,499, or 0.0578%, of Israelis who were vaccinated getting infected in the latest wave.” But what will happen in the long-term no one knows.
fig 38 https://www.israelnationalnews.com/News/News.aspx/309762
Furthermore, if the SARS-CoV-2 virus is indeed a combination of SARS + MERS + HIV then there is reason for concern because their viral genetic material will be contributing some of their characteristics to SARS-CoV-2 virus itself.
The scenario that is unfolding is that vaccinated individuals are responsible for new and emerging variants because new variants of COVID-19 are forming to sidestep the antibodies created by the global vaccination drive as stated by French Virologist and NWO “Controlled Opposition” Dr. Luc Montagnier, “the variants are the product of and result of the vaccination.” He also claims that death curves follow vaccination curves when looking at national data, and says, “I’ll show you that [breakthrough cases] are creating the variants that are resistant to the vaccine.” He says the antibodies created by the virus enable the variants to become stronger and mentions the process of Antibody-dependent Enhancement (ADE).
While ADE is possible within a few weeks post-vaccination it does not explain why there are more SARS-CoV-2 infections among the vaccinated than the unvaccinated.
fig 39 https://www.reuters.com/article/factcheck-vaccine-variants-idUSL2N2NL1M2
The reality is that the vaccinated are producing the variants themselves. You see… the HIV virus has the capacity to produce new HIV variants as it is reproducing inside the body because it’s viral genome is embedded within the human DNA genome. The same is true for the SARS-CoV-2 virus. This is one of the main reasons why science has yet to find a cure for HIV; it keeps on mutating.
Since there are HIV inserts in the SARS-CoV-2 virus it too can mutate within the body! Furthermore the vaccine itself has highjacked the human body in vaccinated people; there is viral RNA in every cell capable of producing similar “spike proteins” as the actual virus. When this happens every cell in the body resembles the COVID-19 virus! The viral mRNA vaccine has turned the body into a virus-like producing machine!
But are vaccinated people contagious? In theory, the viral mRNA vaccine should have only been taken up by cells of the immune system. Scientists are now showing that there is viral RNA in every cell of the body in every organ system! Government, the CDC, Pharmaceuticals, medical authorities ALL REASSURED THE PUBLIC that the viral RNA would be broken down soon after injection and would NOT integrate with human DNA. THEY ALL LIED! This means that should a vaccinated person get infected, because all of their body cells are primed to produce “spike proteins” their cells will resemble an HIV-like virus. Some human cells found in body fluids, blood, nasopharynx region and reproductive organs can be emitted and these cells will have the SAME properties of an HIV-virus. Yes… the vaccinated are contagious! Furthermore, infected cells of the nasopharynx can be released in droplets so airborne transmission is possible.
Everyone was told to get vaccinated, that the vaccine would protect you from variants or result in decreased disease progression should you get infected. None of this was true! Since the new Delta variant has emerged there have been more cases of SARS-CoV-2 infection in vaccinated people than unvaccinated people. A new study by the U.S. Centers for Disease Control and Prevention showed that three-quarters of individuals who became infected with COVID-19 at public events in a Massachusetts county had been fully vaccinated. What they failed to make public from this study was that within that cohort, “
A preliminary analysis matching cluster-associated COVID-19 cases with the state HIV case surveillance data identified 6% cases with verified HIV infection.” Why is this significant? In the United States HIV infection affects only 0.36% of the population. Why is there a rate of 6% HIV positivity in this cohort? A rate that is 17 times the National average?
fig 40 https://www.ctvnews.ca/health/coronavirus/majority-of-covid-19-cases-at-large-public-events-were-among-vaccinated-americans-cdc-study-1.5530634
fig 41 https://www.cdc.gov/mmwr/volumes/70/wr/mm7031e2.htm
This video confirms that the vaccinated are showing similar viral levels or viral loads as the unvaccinated. What does this mean? One would have expected lower viral loads in the vaccinated instead the viral loads are equal. The vaccines are not working like they confirmed they would. AGAIN WE WERE ALL LIED TO! How many more lies before we realize that they are intentionally injecting the public with a bioweapon?
BASICALLY THIS CONFIRMS THAT THE COVID VACCINATED ARE PATHOGENICALLY PRIMED SARS-COV-2 SUPER SPREADERS AND THE VARIANTS ARE COMING FROM THEM!
We suspect the NWO goal was to infect as many people as possible with the vaccine then wait it out till all those infected died off leaving a small cluster of uninfected survivors who would then be either experimented on or turned into slaves. The “useless eaters” are being slowly euthanized through “Gain-of-Function” experimentation… but will we all go gently into the good night?
NIH documents now show that dangerous “Gain-of-Function” research banned in US labs was being outsourced to the Wuhan lab with Dr. Fauci’s approval! Last December, an Australian newspaper reported that COVID injection- makers Pfizer and Astrazeneca were infiltrated by at least 123 CCP loyalists that if called on, would answer directly to the Chinese Communist Party and President Xi himself. And we have shown Moderna collaborates directly with the Chinese Military with Anthony Fauci as their broker!
fig 43 https://coronanews123.wordpress.com/2021/02/24/new-nih-documents-show-fauci-disobeyed-obama-order-to-halt-dangerous-man-made-covid-virus-research-at-wuhan-labs/
fig 44 https://economictimes.indiatimes.com/news/international/world-news/data-leak-reveals-members-of-chinas-communist-party-working-in-global-firms-consulates-report/articleshow/79721469.cms
fig 45 https://trialsitenews.com/did-pfizer-fail-to-perform-industry-standard-animal-testing-prior-to-initiation-of-mrna-clinical-trials/
fig 46. proof.
30 thoughts on “Gain-of-Function Experiments: The SARS-CoV-2/HIV-1 Story”
Gain-of-function? Many scientists-doctors saying the SARS-C0V-2 never actually fulfilled Koch’s postulate, meaning the virus can not sicken perfectly healthy person. If so, C0VID-19 is non existent pandemic. Why nobody are asking? Why U.S. Senator Rand Paul and another Senator Ron Johnson are not asking Fauxi or CDC or NIH if the SARS-C0V-2 virus was ever been isolated?
THE FAUCI/COVID 19 DOSSIER
CC-BY-NC-SA Dr. David E. Martin
This document is prepared for humanity by Dr. David E. Martin.
This work was supported, in part, by a fund-raising effort in which approximately 330 persons contributed funds in support of the New Earth technology team and Urban Global Health Alliance. It is released under a Creative Commons license CCBY-NC-SA. Any derivative use of this dossier must be made public for the benefit of others. All documents, references and disclosures contained herein are subject to an AS-IS representation. The author does not bear responsibility for errors in the public record or references therein. Throughout this document, uses of terms commonly accepted in medical and scientific literature do not imply acceptance or rejection of the dogma that they represent.
Over the past two decades, my company – M·CAM – has been monitoring possible violations of the 1925 Protocol for the Prohibition of the Use in War of Asphyxiating, Poisonous, or other Gases, and of Bacteriological Methods of Warfare (the Geneva Protocol) 1972 Convention on the Prohibition of the Development, Production, and Stockpiling of Bacteriological and Toxin Weapons and Their Destruction (the BTWC). In our 2003-2004 Global Technology Assessment: Vector Weaponization M·CAM highlighted China’s growing involvement in Polymerase Chain Reaction (PCR) technology with respect to joining the world stage in chimeric construction of viral vectors. Since that time, on a weekly basis, we have monitored the development of research and commercial efforts in this field, including, but not limited to, the research synergies forming between the United States Centers for Disease Control and Prevention (CDC), the National Institutes for Allergies and Infectious Diseases (NIAID), the University of North Carolina at Chapel Hill (UNC), Harvard University, Emory University, Vanderbilt University, Tsinghua University, University of Pennsylvania, many other research institutions, and their commercial affiliations.
The National Institute of Health’s grant AI23946-08 issued to Dr. Ralph Baric at the University of North Carolina at Chapel Hill (officially classified as affiliated with Dr. Anthony Fauci’s NIAID by at least 2003) began the work on synthetically altering the Coronaviridae (the coronavirus family) for the express purpose of general research, pathogenic enhancement, detection, manipulation, and potential therapeutic interventions targeting the same. As early as May 21, 2000, Dr. Baric and UNC sought to patent critical sections of the coronavirus family for their commercial benefit.1 In one of the several papers derived from work sponsored by this grant, Dr. Baric published what he reported to be the full length cDNA of SARS CoV in which it was clearly stated that SAR CoV was based on a composite of DNA segments.
“Using a panel of contiguous cDNAs that span the entire genome, we have assembled a full-length cDNA of the SARS-CoV Urbani strain, and have rescued molecularly cloned SARS viruses (infectious clone SARS-CoV) that contained the expected marker mutations inserted into the component clones.”2
On April 19, 2002 – the Spring before the first SARS outbreak in Asia – Christopher M. Curtis, Boyd Yount, and Ralph Baric filed an application for U.S. Patent 7,279,372 for a method of producing recombinant coronavirus. In the first public record of the claims, they sought to patent a means of producing, “an infectious, replication defective, coronavirus.” This work was supported by the NIH grant referenced above and GM63228. In short, the U.S. Department of Health and Human Services was involved in the funding of amplifying the infectious nature of coronavirus between 1999 and 2002 before SARS was ever detected in humans.
1 U.S. Provisional Application No. 60/206,537, filed May 21, 2000
Against this backdrop, we noted the unusual patent prosecution efforts of the CDC, when on April 25, 2003 they sought to patent the SARS coronavirus isolated from humans that had reportedly transferred to humans during the 2002-2003 SARS outbreak in Asia. 35 U.S.C. §101 prohibits patenting nature. This legality did not deter CDC in their efforts. Their application, updated in 2007, ultimately issued as U.S. Patent 7,220,852 and constrained anyone not licensed by their patent from manipulating SARS CoV, developing tests or kits to measure SARS coronavirus in humans or working with their patented virus for therapeutic use. Work associated with this virus by their select collaborators included considerable amounts of chimeric engineering, gain-of-function studies, viral characterization, detection, treatment (both vaccine and therapeutic intervention), and weaponization inquiries.
In short, with Baric’s U.S. Patent 6,593,111 (Claims 1 and 5) and CDC’s ‘852 patent (Claim 1), no research in the United States could be conducted without permission or infringement.
We noted that gain-of-function specialist, Dr. Ralph Baric, was both the recipient of millions of dollars of U.S. research grants from several federal agencies but also sat on the World Health Organization’s International Committee on Taxonomy of Viruses (ICTV) and the Coronaviridae Study Group (CSG). In this capacity, he was both responsible for determining “novelty” of clades of virus species but directly benefitted from determining declarations of novelty in the form of new research funding authorizations and associated patenting and commercial collaboration. Together with CDC, NIAID, WHO, academic and commercial parties (including Johnson & Johnson; Sanofi and their several coronavirus patent holding biotech companies; Moderna; Ridgeback; Gilead; Sherlock Biosciences; and, others), a powerful group of interests constituted what we would suggest are “interlocking directorates” under U.S. anti-trust laws.
These entities also were affiliated with the WHO’s Global Preparedness Monitoring Board (GPMB) whose members were instrumental in the Open Philanthropy-funded global coronavirus pandemic “desk-top” exercise EVENT 201 in October 2019. This event, funded by the principal investor in Sherlock Biosciences and linking interlocking funding partner, the Bill and Melinda Gates Foundation into the GPMB mandate for a respiratory disease global preparedness exercise to be completed by September 2020 alerted us to anticipate an “epidemic” scenario. We expected to see such a scenario emerge from Wuhan or Guangdong China, northern Italy, Seattle, New York or a combination thereof, as Dr. Zhengli Shi and Dr. Baric’s work on zoonotic transmission of coronavirus identified overlapping mutations in coronavirus in bat populations located in these areas.
This dossier is by no means exhaustive. It is, however, indicative the numerous criminal violations that may be associated with the COVID-19 terrorism. All source materials are referenced herein. An additional detailed breakdown of all the of individuals, research institutions, foundations, funding sources, and commercial enterprises can be accessed upon request.
Dr. David E. Martin reveals shocking news everyone, especially Canadians, MUST ACT on NOW! Proof of Treason and Crimes Against Humanity.
The lipid nano particle delivery system for the mRNA injections (Pfizer and Moderna) was developed at UBC with federal government funding. Trudeau and the government have a financial stake in the “vaccines.”
Dr. David E. Martin: http://www.DavidMartin.World.com
The Fauci COVID-19 Dossier: https://www.davidmartin.world/wp-content/uploads/2021/01/The_Fauci_COVID-19_Dossier.pdf
Reiner Fuelmich interview:
Transcript of Interview: https://drive.google.com/file/d/19o1BeQa6z9XD58GkYE1e-qiiNbnr5wTz/view
Stew Peters interviews with Dr. David Martin:
Reiner Fuelmich interview:
Here’s a helpful audio of useful and insightful listening for commonwealth folk .. https://soundcloud.com/tantramar-landowners/tracks