Yes, it's the argument of pointing a gun at someone's head and telling him "hand over your money or I'll blow your brains out" then than trying to tell the judge "your honor, he gave me money of his own free choice".
When you look at the funding streams for EcoHealth Alliance, Metabiota, Labyrinth Global Health, and so on, they point straight back towards DARPA, DTRA, USAID, In-Q-Tel, and the outsourcing of the US biodefense network to foreign biolabs that began in the late 2000s in response to increased scrutiny of US-based BSL-3 and BSL-4 lab construction.
Right after a big congressional hearing where Edward Hammond and Gigi Gronvall faced off against each other on the issue, Nathan Wolfe, a known associate of Jeffrey Epstein and Ghislaine Maxwell and likely CIA asset, started Global Viral (which was later spun off into Metabiota), and then the US DOD, HHS, and USAID started paying these "virus-hunting NGO middlemen" to subcontract grants to labs all over the place under programs like the CBEP/BTRP and EPT-PREDICT.
Hunter Biden was instrumental in funding and assisting a company responsible for Ukraine biolabs. The Metabiota company, headed by a Ghislaine Maxwell partner named Nathan Wolfe, was in charge of setting up biolabs in Ukraine. The biolabs have sparked concern that dangerous materials could be...
nationalfile.com
It's not just the WIV, but also biolabs in Ukraine, Georgia, various West African nations in Ebola hotspots, and also in Laos, Cambodia, and other parts of Southeast Asia.
The US Army regularly produces deadly viruses, bacteria and toxins in direct violation of the UN Convention on the prohibition of Biological Weapons
silview.media
There is no valid purpose for GOF research, whatsoever. If you listen to Francis Boyle or Richard Ebright, it's basically a euphemism for offensive bioweapon research.
Dennis Carroll at USAID was instrumental in all of this. He was the lynchpin linking the likes of Peter Daszak, Nathan Wolfe, and Karen Saylors together.
A USAID official greased the skids for a controversial "virus hunting" organization with taxpayer funds.
usrtk.org
Andrew Huff, the former VP of EcoHealth Alliance turned whistleblower, and came forward and made a statement that Peter Daszak confided in him that he was working for the CIA.
The same exact DARPA/DTRA bio-mafia also funded the development of COVID-19 vaccines, through programs like ADEPT: PROTECT, Operation Warp Speed, and the ACTIV partnership led by the DOD. The components that go into these vaccines come from defense contractors like Emergent BioSolutions and National Resilience.
So, the US DOD funded both the creation of SARS-CoV-2, and the development of the vaccine against it. You know what that is? That's fraud, racketeering, and democide.
UPDATED 13 FEB 23: This timeline contains most of the relevant major dates, events, entities and legislation for the COVID-19 enterprise fraud construct and features links to sourced and cited work…
politicalmoonshine.com
For the democidal military-industrial complex and intelligence nutcases behind this, there is no putting the genie back in the bottle. We know what they did.
This stuff makes sense if you realize that elites/globalists/reptillians/whateveryoucallthemasters, operate off of a ritualistic and pretty predictable mindset.
In their view they are exempt from guilt/blame/responsibility if they don't directly and forcibly make you do stuff.
It's why for the most part there wasn't government goons running around jabbing people up.
Anyone who took the vaccine took it under their own volition. Were they coerced? Sure. Bribed? Of course. Persuaded? Certainly.
But directly forced to take it? Not really. So in the minds of these creeps they are exempt from any blame of the vaxx.
They do this for almost everything as well, in particular a common trope of theirs is to tell you what they are going to do before they do it, often pretty overtly too. They do it for the same reason, if they tell you that you're going to live in the pod and eat the bugs, and you don't immediately cut the head off the proverbial snake. You must've wanted the changes!
They 100% seriously believe that exact scenario is morally okay. After all you could've just not given him the money...Consequences not being mentioned.
This mind set is pretty normal for an elite that has gone into a terminal death spiral. The french nobility before the revolution was much the same, as was the sentorial class before ceasar, and deep down inside they know thier fucked in the long term. You can see it in them.
Perhaps its only fitting that the children of Robperre suffer the same fate as the ancient regieme they anhilated.
At first, way back in 2020, some people were concerned that SARS-CoV-2 would prove impossible to vaccinate against due to Dengue-like ADE, or antibody-dependent enhancement of infection (which SARS was suspected to have). This is a known phenomenon where incomplete antibody neutralization of a pathogen leads to enhanced infection, with live virus hitching a ride into macrophages via the Fc receptor and infecting them. This doesn't happen in all viruses, only a certain subset of them. That's how Dengvaxia failed. When given to children in the Philippines who were seronegative for Dengue, the vaccine actually caused enhanced infection.
As it turns out, this was not the only thing to be concerned about, when it came to the Spike protein and the mRNA vaccines. Not even close. Every component of the vaccines is harmful and cytotoxic, including the Spike protein itself.
The whole concept of a gene-encoded vaccine using human cells as in vivo bioreactors grew out of a DARPA program called ADEPT: PROTECT and P3 (the Pandemic Prevention Platform). Around a decade ago, DARPA started funding Moderna to the tune of millions of dollars to come up with a gene-encoded monoclonal antibody therapy against Chikungunya virus called mRNA-1944. This is military technology and all the people working on it behind the scenes are spook-adjacent.
The key thing here to keep in mind is that the mode of action between mRNA encoding a monoclonal antibody and mRNA encoding a viral antigen is completely different. Yes, they both use the same delivery mechanism of introducing foreign mRNA into human cells and having those cells act as little bioreactors and manufacture biologics using their own ribosomes. However, that's where the similarities end.
With mRNA mAb therapy, the goal is to get cells to produce and export a monoclonal antibody against a selected pathogen. With an mRNA vaccine, the goal is to get cells to produce a viral protein and present it (and its fragments, via MHC) on their surfaces. The former produces antibodies that bind and neutralize pathogens. The latter makes the immune system confuse the transfected cell for a virus and attack it.
COVID-19 vaccines are causing myocarditis, pericarditis, aortic dissection, bone marrow suppression, diabetes, brain inflammation, and so on, and so forth, because the lipid nanoparticles don't stay in the shoulder and aren't specific to deltoid muscle tissue. They travel all over the body, transfecting heart muscle tissue, bone marrow, brain cells, reproductive tissues, the other vital organs, et cetera, and making them produce and present Spike on their surfaces. These proteins have a transmembrane domain in the base, so they anchor into cell walls facing outward, into the extracellular space, making the affected cells look very much like viruses to the immune system. Leukocytes recognize whole particles. They don't just harmlessly form antibodies against viral antigens being produced by human cells. They see the protein, recognize the whole cell as a foreign body, and try to phagocytize and destroy it. The easiest way to visualize what is happening here is to imagine that the transfected cells are behaving like rejected transplants, because that's what the vaccine is turning them into; foreign objects. The tissue damage is caused by the immune response. To be specific, leukocytes eating holes in the tissue. That's where the heart scarring comes from.
The delivery mechanism is toxic, the mRNA is toxic, and the protein itself is toxic.
The synthetic cationic lipids used for mRNA delivery are highly inflammatory, to the point where they don't even bother including any adjuvants in these vaccines because the lipid nanoparticles are, themselves, plenty inflammatory enough to stimulate an immune response.
The mRNA in these vaccines is not natural mRNA, but modRNA, or RNA where all the uracil has been replaced with pseudouridylyl, such that every U in the sequence is Ψ instead. So, instead of the bases in this RNA being Adenine, Guanine, Cytosine, and Uracil, it's Adenine, Guanine, Cytosine, and Pseudouridylyl. The reason why they do this is because Katalin Kariko (who just received a Nobel Prize alongside Drew Weissman, ridiculously enough) showed in a 2005 paper that mRNA can be cloaked from endosomal TLRs (receptors that detect foreign objects and set off inflammatory cascades, like little smoke alarms) by swapping U with Ψ. The resulting mRNA is called modRNA or "nucleoside-modified mRNA". This modRNA is way more stable and lasts longer inside the body because ribonucleases don't know what to do with Ψ or how to break down and recycle these things. In other words, cells transfected with this mRNA could be pumping out Spike protein for weeks or months on end. They don't really know.
This is bad, because SARS-CoV-2 Spike is extremely toxic by multiple mechanisms. SARS-CoV-2 Spike is vasculotoxic and cardiotoxic, attacks blood vessels, and permeabilizes the blood-brain barrier. It is highly inflammatory, with a superantigenic region and an LPS-binding region. Because it binds bacterial lipopolysaccharides (endotoxins), it can enhance the inflammatory effect of bacteria already in the body. Think of the irony of that. Vaccine manufacturers go out of their way to make sure their vaccine batches aren't tainted with bacterial endotoxin using LAL tests (limulus amebocyte lysate) made from horseshoe crab blood, and yet, in this instance, they're inducing human cells to manufacture a protein that binds and accentuates the inflammatory effect of, you guessed it, bacterial endotoxins.
That's not even the worst part. SARS-CoV-2 Spike is laced with amyloidogenic motifs, and binds and aggregates amyloid beta, tau, and prion proteins. Some of the people who received this vaccine may end up with Parkinson's, Alzheimer's, Dementia, Creutzfeldt-Jakob, or other neurodegenerative diseases down the line, because of this. The LNPs carrying the modRNA readily bypass the blood-brain barrier and they absolutely do transfect brain tissue and induce the recipient to make this protein in their brains.
SARS-CoV-2 Spike, when digested by neutrophil elastase or other enzymes, has been shown to aggressively form amyloid-fibrin clots, purely out of protein, even in platelet-poor plasma.
SARS-CoV-2 Spike also has a nuclear localization signal and may travel to the nucleus and interfere with DNA repair mechanisms like p53 and BRCA, which means more cancers, and more aggressive tumor formation.
As if all this wasn't bad enough, to add insult to injury, the people who received these vaccines are experiencing IgG4 class switches, where their antibody response to SARS-CoV-2 Spike is switching from neutralizing antibodies to antibodies that essentially instruct the immune system to treat the Spike as an allergen and leave it alone. For obvious reasons, you don't want this to happen with a virus.
To make matters even worse, Kevin McKernan and various independent laboratories have confirmed that the Pfizer vaccine is heavily contaminated with plasmid DNA and the SV40 promoter sequence, which could very easily enter cell nuclei and genetically transform those cells. And the mRNA has been detected in the breast milk of vaccinated mothers, too. And it causes vaginal bleeding in postmenopausal women.
This was all intentional. Katherine Watt, Sasha Latypova, and Whitney Webb lay out, in extensive detail, how the US Government slowly eroded consumer protections against exactly this scenario, and how the vaccines were procured by the US DOD under an OTA as "medical countermeasures" not legally regulated as pharmaceuticals of any kind. That FDA approval? Completely pointless. The FDA approved them under color of law. The FDA does not have the authority to regulate OTAs procured by the DOD, because they're not pharmaceuticals, but "medical countermeasures". As in, weapons. The raw materials for these vaccines came from defense contractors like Emergent BioSolutions (a.k.a. BioPort) and National Resilience. The whole thing was a military operation coordinated by Operation Warp Speed and ACTIV.
Yes, the Pentagon just poisoned hundreds of millions of American citizens, and over a million military personnel.
It is estimated that the COVID-19 vaccines are, in fact, killing 1 in 800 of their recipients, or 17 million people worldwide so far. This is a historical mass casualty event that is being completely ignored by the media.
The situation we are dealing with here is not an accident, but one of our governments being filled with mass-murdering maniacs.
At first, way back in 2020, some people were concerned that SARS-CoV-2 would prove impossible to vaccinate against due to Dengue-like ADE, or antibody-dependent enhancement of infection (which SARS was suspected to have). This is a known phenomenon where incomplete antibody neutralization of a pathogen leads to enhanced infection, with live virus hitching a ride into macrophages via the Fc receptor and infecting them. This doesn't happen in all viruses, only a certain subset of them. That's how Dengvaxia failed. When given to children in the Philippines who were seronegative for Dengue, the vaccine actually caused enhanced infection.
As it turns out, this was not the only thing to be concerned about, when it came to the Spike protein and the mRNA vaccines. Not even close. Every component of the vaccines is harmful and cytotoxic, including the Spike protein itself.
The whole concept of a gene-encoded vaccine using human cells as in vivo bioreactors grew out of a DARPA program called ADEPT: PROTECT and P3 (the Pandemic Prevention Platform). Around a decade ago, DARPA started funding Moderna to the tune of millions of dollars to come up with a gene-encoded monoclonal antibody therapy against Chikungunya virus called mRNA-1944. This is military technology and all the people working on it behind the scenes are spook-adjacent.
The key thing here to keep in mind is that the mode of action between mRNA encoding a monoclonal antibody and mRNA encoding a viral antigen is completely different. Yes, they both use the same delivery mechanism of introducing foreign mRNA into human cells and having those cells act as little bioreactors and manufacture biologics using their own ribosomes. However, that's where the similarities end.
With mRNA mAb therapy, the goal is to get cells to produce and export a monoclonal antibody against a selected pathogen. With an mRNA vaccine, the goal is to get cells to produce a viral protein and present it (and its fragments, via MHC) on their surfaces. The former produces antibodies that bind and neutralize pathogens. The latter makes the immune system confuse the transfected cell for a virus and attack it.
COVID-19 vaccines are causing myocarditis, pericarditis, aortic dissection, bone marrow suppression, diabetes, brain inflammation, and so on, and so forth, because the lipid nanoparticles don't stay in the shoulder and aren't specific to deltoid muscle tissue. They travel all over the body, transfecting heart muscle tissue, bone marrow, brain cells, reproductive tissues, the other vital organs, et cetera, and making them produce and present Spike on their surfaces. These proteins have a transmembrane domain in the base, so they anchor into cell walls facing outward, into the extracellular space, making the affected cells look very much like viruses to the immune system. Leukocytes recognize whole particles. They don't just harmlessly form antibodies against viral antigens being produced by human cells. They see the protein, recognize the whole cell as a foreign body, and try to phagocytize and destroy it. The easiest way to visualize what is happening here is to imagine that the transfected cells are behaving like rejected transplants, because that's what the vaccine is turning them into; foreign objects. The tissue damage is caused by the immune response. To be specific, leukocytes eating holes in the tissue. That's where the heart scarring comes from.
The delivery mechanism is toxic, the mRNA is toxic, and the protein itself is toxic.
The synthetic cationic lipids used for mRNA delivery are highly inflammatory, to the point where they don't even bother including any adjuvants in these vaccines because the lipid nanoparticles are, themselves, plenty inflammatory enough to stimulate an immune response.
The mRNA in these vaccines is not natural mRNA, but modRNA, or RNA where all the uracil has been replaced with pseudouridylyl, such that every U in the sequence is Ψ instead. So, instead of the bases in this RNA being Adenine, Guanine, Cytosine, and Uracil, it's Adenine, Guanine, Cytosine, and Pseudouridylyl. The reason why they do this is because Katalin Kariko (who just received a Nobel Prize alongside Drew Weissman, ridiculously enough) showed in a 2005 paper that mRNA can be cloaked from endosomal TLRs (receptors that detect foreign objects and set off inflammatory cascades, like little smoke alarms) by swapping U with Ψ. The resulting mRNA is called modRNA or "nucleoside-modified mRNA". This modRNA is way more stable and lasts longer inside the body because ribonucleases don't know what to do with Ψ or how to break down and recycle these things. In other words, cells transfected with this mRNA could be pumping out Spike protein for weeks or months on end. They don't really know.
This is bad, because SARS-CoV-2 Spike is extremely toxic by multiple mechanisms. SARS-CoV-2 Spike is vasculotoxic and cardiotoxic, attacks blood vessels, and permeabilizes the blood-brain barrier. It is highly inflammatory, with a superantigenic region and an LPS-binding region. Because it binds bacterial lipopolysaccharides (endotoxins), it can enhance the inflammatory effect of bacteria already in the body. Think of the irony of that. Vaccine manufacturers go out of their way to make sure their vaccine batches aren't tainted with bacterial endotoxin using LAL tests (limulus amebocyte lysate) made from horseshoe crab blood, and yet, in this instance, they're inducing human cells to manufacture a protein that binds and accentuates the inflammatory effect of, you guessed it, bacterial endotoxins.
That's not even the worst part. SARS-CoV-2 Spike is laced with amyloidogenic motifs, and binds and aggregates amyloid beta, tau, and prion proteins. Some of the people who received this vaccine may end up with Parkinson's, Alzheimer's, Dementia, Creutzfeldt-Jakob, or other neurodegenerative diseases down the line, because of this. The LNPs carrying the modRNA readily bypass the blood-brain barrier and they absolutely do transfect brain tissue and induce the recipient to make this protein in their brains.
SARS-CoV-2 Spike, when digested by neutrophil elastase or other enzymes, has been shown to aggressively form amyloid-fibrin clots, purely out of protein, even in platelet-poor plasma.
SARS-CoV-2 Spike also has a nuclear localization signal and may travel to the nucleus and interfere with DNA repair mechanisms like p53 and BRCA, which means more cancers, and more aggressive tumor formation.
As if all this wasn't bad enough, to add insult to injury, the people who received these vaccines are experiencing IgG4 class switches, where their antibody response to SARS-CoV-2 Spike is switching from neutralizing antibodies to antibodies that essentially instruct the immune system to treat the Spike as an allergen and leave it alone. For obvious reasons, you don't want this to happen with a virus.
To make matters even worse, Kevin McKernan and various independent laboratories have confirmed that the Pfizer vaccine is heavily contaminated with plasmid DNA and the SV40 promoter sequence, which could very easily enter cell nuclei and genetically transform those cells. And the mRNA has been detected in the breast milk of vaccinated mothers, too. And it causes vaginal bleeding in postmenopausal women.
This was all intentional. Katherine Watt, Sasha Latypova, and Whitney Webb lay out, in extensive detail, how the US Government slowly eroded consumer protections against exactly this scenario, and how the vaccines were procured by the US DOD under an OTA as "medical countermeasures" not legally regulated as pharmaceuticals of any kind. That FDA approval? Completely pointless. The FDA approved them under color of law. The FDA does not have the authority to regulate OTAs procured by the DOD, because they're not pharmaceuticals, but "medical countermeasures". As in, weapons. The raw materials for these vaccines came from defense contractors like Emergent BioSolutions (a.k.a. BioPort) and National Resilience. The whole thing was a military operation coordinated by Operation Warp Speed and ACTIV.
Yes, the Pentagon just poisoned hundreds of millions of American citizens, and over a million military personnel.
It is estimated that the COVID-19 vaccines are, in fact, killing 1 in 800 of their recipients, or 17 million people worldwide so far. This is a historical mass casualty event that is being completely ignored by the media.
The situation we are dealing with here is not an accident, but one of our governments being filled with mass-murdering maniacs.
At first, way back in 2020, some people were concerned that SARS-CoV-2 would prove impossible to vaccinate against due to Dengue-like ADE, or antibody-dependent enhancement of infection (which SARS was suspected to have). This is a known phenomenon where incomplete antibody neutralization of a pathogen leads to enhanced infection, with live virus hitching a ride into macrophages via the Fc receptor and infecting them. This doesn't happen in all viruses, only a certain subset of them. That's how Dengvaxia failed. When given to children in the Philippines who were seronegative for Dengue, the vaccine actually caused enhanced infection.
As it turns out, this was not the only thing to be concerned about, when it came to the Spike protein and the mRNA vaccines. Not even close. Every component of the vaccines is harmful and cytotoxic, including the Spike protein itself.
The whole concept of a gene-encoded vaccine using human cells as in vivo bioreactors grew out of a DARPA program called ADEPT: PROTECT and P3 (the Pandemic Prevention Platform). Around a decade ago, DARPA started funding Moderna to the tune of millions of dollars to come up with a gene-encoded monoclonal antibody therapy against Chikungunya virus called mRNA-1944. This is military technology and all the people working on it behind the scenes are spook-adjacent.
The key thing here to keep in mind is that the mode of action between mRNA encoding a monoclonal antibody and mRNA encoding a viral antigen is completely different. Yes, they both use the same delivery mechanism of introducing foreign mRNA into human cells and having those cells act as little bioreactors and manufacture biologics using their own ribosomes. However, that's where the similarities end.
With mRNA mAb therapy, the goal is to get cells to produce and export a monoclonal antibody against a selected pathogen. With an mRNA vaccine, the goal is to get cells to produce a viral protein and present it (and its fragments, via MHC) on their surfaces. The former produces antibodies that bind and neutralize pathogens. The latter makes the immune system confuse the transfected cell for a virus and attack it.
COVID-19 vaccines are causing myocarditis, pericarditis, aortic dissection, bone marrow suppression, diabetes, brain inflammation, and so on, and so forth, because the lipid nanoparticles don't stay in the shoulder and aren't specific to deltoid muscle tissue. They travel all over the body, transfecting heart muscle tissue, bone marrow, brain cells, reproductive tissues, the other vital organs, et cetera, and making them produce and present Spike on their surfaces. These proteins have a transmembrane domain in the base, so they anchor into cell walls facing outward, into the extracellular space, making the affected cells look very much like viruses to the immune system. Leukocytes recognize whole particles. They don't just harmlessly form antibodies against viral antigens being produced by human cells. They see the protein, recognize the whole cell as a foreign body, and try to phagocytize and destroy it. The easiest way to visualize what is happening here is to imagine that the transfected cells are behaving like rejected transplants, because that's what the vaccine is turning them into; foreign objects. The tissue damage is caused by the immune response. To be specific, leukocytes eating holes in the tissue. That's where the heart scarring comes from.
The delivery mechanism is toxic, the mRNA is toxic, and the protein itself is toxic.
The synthetic cationic lipids used for mRNA delivery are highly inflammatory, to the point where they don't even bother including any adjuvants in these vaccines because the lipid nanoparticles are, themselves, plenty inflammatory enough to stimulate an immune response.
The mRNA in these vaccines is not natural mRNA, but modRNA, or RNA where all the uracil has been replaced with pseudouridylyl, such that every U in the sequence is Ψ instead. So, instead of the bases in this RNA being Adenine, Guanine, Cytosine, and Uracil, it's Adenine, Guanine, Cytosine, and Pseudouridylyl. The reason why they do this is because Katalin Kariko (who just received a Nobel Prize alongside Drew Weissman, ridiculously enough) showed in a 2005 paper that mRNA can be cloaked from endosomal TLRs (receptors that detect foreign objects and set off inflammatory cascades, like little smoke alarms) by swapping U with Ψ. The resulting mRNA is called modRNA or "nucleoside-modified mRNA". This modRNA is way more stable and lasts longer inside the body because ribonucleases don't know what to do with Ψ or how to break down and recycle these things. In other words, cells transfected with this mRNA could be pumping out Spike protein for weeks or months on end. They don't really know.
This is bad, because SARS-CoV-2 Spike is extremely toxic by multiple mechanisms. SARS-CoV-2 Spike is vasculotoxic and cardiotoxic, attacks blood vessels, and permeabilizes the blood-brain barrier. It is highly inflammatory, with a superantigenic region and an LPS-binding region. Because it binds bacterial lipopolysaccharides (endotoxins), it can enhance the inflammatory effect of bacteria already in the body. Think of the irony of that. Vaccine manufacturers go out of their way to make sure their vaccine batches aren't tainted with bacterial endotoxin using LAL tests (limulus amebocyte lysate) made from horseshoe crab blood, and yet, in this instance, they're inducing human cells to manufacture a protein that binds and accentuates the inflammatory effect of, you guessed it, bacterial endotoxins.
That's not even the worst part. SARS-CoV-2 Spike is laced with amyloidogenic motifs, and binds and aggregates amyloid beta, tau, and prion proteins. Some of the people who received this vaccine may end up with Parkinson's, Alzheimer's, Dementia, Creutzfeldt-Jakob, or other neurodegenerative diseases down the line, because of this. The LNPs carrying the modRNA readily bypass the blood-brain barrier and they absolutely do transfect brain tissue and induce the recipient to make this protein in their brains.
SARS-CoV-2 Spike, when digested by neutrophil elastase or other enzymes, has been shown to aggressively form amyloid-fibrin clots, purely out of protein, even in platelet-poor plasma.
SARS-CoV-2 Spike also has a nuclear localization signal and may travel to the nucleus and interfere with DNA repair mechanisms like p53 and BRCA, which means more cancers, and more aggressive tumor formation.
As if all this wasn't bad enough, to add insult to injury, the people who received these vaccines are experiencing IgG4 class switches, where their antibody response to SARS-CoV-2 Spike is switching from neutralizing antibodies to antibodies that essentially instruct the immune system to treat the Spike as an allergen and leave it alone. For obvious reasons, you don't want this to happen with a virus.
To make matters even worse, Kevin McKernan and various independent laboratories have confirmed that the Pfizer vaccine is heavily contaminated with plasmid DNA and the SV40 promoter sequence, which could very easily enter cell nuclei and genetically transform those cells. And the mRNA has been detected in the breast milk of vaccinated mothers, too. And it causes vaginal bleeding in postmenopausal women.
This was all intentional. Katherine Watt, Sasha Latypova, and Whitney Webb lay out, in extensive detail, how the US Government slowly eroded consumer protections against exactly this scenario, and how the vaccines were procured by the US DOD under an OTA as "medical countermeasures" not legally regulated as pharmaceuticals of any kind. That FDA approval? Completely pointless. The FDA approved them under color of law. The FDA does not have the authority to regulate OTAs procured by the DOD, because they're not pharmaceuticals, but "medical countermeasures". As in, weapons. The raw materials for these vaccines came from defense contractors like Emergent BioSolutions (a.k.a. BioPort) and National Resilience. The whole thing was a military operation coordinated by Operation Warp Speed and ACTIV.
Yes, the Pentagon just poisoned hundreds of millions of American citizens, and over a million military personnel.
It is estimated that the COVID-19 vaccines are, in fact, killing 1 in 800 of their recipients, or 17 million people worldwide so far. This is a historical mass casualty event that is being completely ignored by the media.
The situation we are dealing with here is not an accident, but one of our governments being filled with mass-murdering maniacs.
I feel bad for my friends who were forced or duped into it.
I am laughing at those who tried to force it on others. I hope they take the brunt of the suffering. But I am deeply sad for people who were against mandates and just wanted to keep their jobs and provide for their families.
Weird that the pro vaxxers like vaermina or however he spells it, have been silent on this site for quite some time.
I feel bad for my friends who were forced or duped into it.
I am laughing at those who tried to force it on others. I hope they take the brunt of the suffering. But I am deeply sad for people who were against mandates and just wanted to keep their jobs and provide for their families.
Weird that the pro vaxxers like vaermina or however he spells it, have been silent on this site for quite some time.
It was his/her hill to die on, since he/she called us all "conspiracy theorists" and the like for seeing this shit for what it was when it was happening.
Now this proverbial hill may be a literal one, if he/she got the vax.
It was his/her hill to die on, since he/she called us all "conspiracy theorists" and the like for seeing this shit for what it was when it was happening.
Now this proverbial hill may be a literal one, if he/she got the vax.
My stance back then was essentially, "this is brand new, there's no long term studies, there's no phase 3 clinical trials, I'm taking a wait and see approach," and guess what? I waited. I saw.
That was the smart approach.
I also held that if this worked as advertised, it's a revolutionary technology that will change vaccination forever. It was a failure.
It was his/her hill to die on, since he/she called us all "conspiracy theorists" and the like for seeing this shit for what it was when it was happening.
Now this proverbial hill may be a literal one, if he/she got the vax.
My stance back then was essentially, "this is brand new, there's no long term studies, there's no phase 3 clinical trials, I'm taking a wait and see approach," and guess what? I waited. I saw.
I Found Manga about more succesfull virus used to decimate humanity.Basically ,Germans win WW2,form world goverment,rule world - and decide,that there is too many humans,like Gates and Soros now.
Difference is,instead of weak Wuhan virus they created P-Flu virus changing people into zombie - and start killing them,and all people nearby.
Here,chapter which explain how it happened:
In the near future where Android (A.I) becomes common among humans, a virus outbreak suddenly occurred, turning over 70% humanity into zombie-like Creatures. The A.I soon break away from their infected owners since they're not programmed to recognize Creatures as humans, but one of them, the...
mangakakalot.com
I quess,that our overlords wonted the same,but since they gave developing it to China.....
You think that’s bad? Here's Michael Yeadon saying they're toxic by design:
One of the guys who wrote this paper is now standing on street corners and begging passersby to listen, because he looked closely at the phylogenetic data of SARS-CoV-2 and finally realized what I already knew a couple years ago, which is that the virus was engineered and released intentionally and maliciously, multiple times:
The trouble with calling it Nuremberg 2.0, is the people behind this nonsense aren't Nazis. They're the people who hate Nazis (for better or for worse).
The trouble with calling it Nuremberg 2.0, is the people behind this nonsense aren't Nazis. They're the people who hate Nazis (for better or for worse).
The context is that it's a colloquialism for a massive trial for those who've committed crimes against humanity on such a large, terrible scale.
It's also ironic because if the vaccines are killing one in eight people worldwide, all the people who developed, pushed, and peddled the vaxx may have killed as many as the Nazis did, if not more.
If the worst theories about this are true and it was a depopulation plot of some kind for ideological reasons, and it weren't just because of plain old greed, than they're no better than the Nazis.
The trouble with calling it Nuremberg 2.0, is the people behind this nonsense aren't Nazis. They're the people who hate Nazis (for better or for worse).
They might not be literal National Socialists, but there is much in common between them and the historical Nazis, in regard to human rights and so on..