Dr. Joseph Sansone explains the first international judicial declaration labeling mRNA vaccines as bioweapons—and his push to outlaw them through state legislation.
It should infuriate every American that our President just wined and dinned the Big Pharma Snake Bourla at our White House, praised him for doing such a good job on the mRNA poison and gave him BILLIONS more tax payer dollars for MORE POISON. They are just poking us in the eye, this is pure evil.
IMHO - While the binary question of toxin versus not, seems to flip a legal switch on whether this is a bioweapon, that’s not logical. We need to remember that all drugs are toxic (with an R factor) because they are patented, manmade, exogenous factors and function neither within a normal biological range of chemistry nor natural in its ingredients.
Is the dispositive point for the court that the quality control on such toxic products as a pharmaceutical product like these shots needs to be identified and confirmed by the regulatory authorities based on suppliers’ test data, but was not? Rather, our US regulators colluded with suppliers to distribute toxic products for profit, without upholding their responsibility for protecting public safety. Can we call it reckless disregard, willful negligence and racketeering?
If you want to see my years of research on the COVID "vaccine" bioweapon including spiritual connections, gematria, and links to scientific results and more. go to:
Well, none of them had bills that said the shots were already illegal according to existing bioweapons or weapons of mass destruction laws and created a criminal and civil liability for non enforcement. The point is to get it introduced in as many places as possible to create pressure.
Why dr Joe, you are being over the world known now, quite impressive for a one person show and agit. But you and a few more people, like Ana and Karen, certainly merit all the attention y ou get these days. One only wonders, w hat took t he rest of the world so long? The facts have been t here open for all to see, so no eyes? no brains? no guts? or what are these people missing?
International Tribunal Declares COVID mRNA Injections 'Biological and Technological Weapons of Mass Destruction' International Tribunal Declares COVID mRNA Injections 'Biological Weapons of Mass Destruction. Dr. Joseph Sansone explains the first international judicial declaration labelling mRNA vaccines as bioweapons.
DEADLY Covid mRNA injections are, at last, formally declared and certified by a 'Sovereign Nation', as 'Bioweapons of Mass Destruction'!
At long last, the truth, reality and common sense are beginning to surface!
Big Pharma can't hide this depopulation Plan for much longer. They will have to relinquish their 'PREP Act' shield to prosecution for causing masses of 'VAX' injuries and VAX-related DEATHS.
This is total batshit crazy mis-information. The author is a crazy therapist of dubious value way out of his lane. This channel is facilitating false information about vaccines which are the pinnacle of medical science. Why do people attack phenomenal things? A case in point: why was Caitlin Clark assaulted by her fellow basketball players for the past 2 years. An exceptional basketball player, an exceptional vaccination with irrational illogical violent attackers. Senseless, useless, harmful
I wish. I’m about to get one . Thanks for asking. Substantially less chances for COVID-19, long sequelae, susceptibility to other illnesses like MIs, CVAs, HTN, DM and CHF. Pus being sick and out of commission is not my cup of tea. Basically I’ve never seen or heard of a vaccine that I didn’t want. I wish I could get several vaccines that I’m not eligible for.
Right? To become a walking bioweapon oneself who's shedding all those toxins on those in proximity has to be the absolute mark of a moron who in wishing they could get MORE "vaccines" wonders why they keep getting sick. You have to wonder how they made it this far in life. The gatekeepers in these comments floor me.
Colby Wang, you have been horribly misinformed and misled.
More people need to understand that it is not enough for there to be no mandates...
The modified mRNA-LNP gene "therapy" transfection injections are dangerous by design.
And they can shed on others, making them dangerous for those who said "Hell NO!" as well...
Self vs Non-self is basic foundational Immunology 101...But the mRNA shots undermine this essential principle.
The mRNA shots were/are always going to be an immunological catastrophe for humanity.
The mechanism of action (using mRNA instructions to turn one’s own cells into foreign non-self “spike protein factories”) is the primary mechanism of harm.
The primary danger of the COVID-19 mRNA injections has always been one’s own immune system’s attack response by the mighty CD8+ Cytotoxic T Lymphocyte cells (AKA Killer T-cells):
The COVID-19 mRNA injections must be recalled from the market and mRNA-based products must be banned because the modified mRNA-LNP genetic technology platform is fundamentally flawed & dangerous by design.
These modified mRNA-LNP COVID-19 injections, that trigger one's own immune system to attack & kill one's own formerly healthy cells (that have been instructed to produce/express foreign, non-self proteins), no matter where those cells are in the body, never should have been made available to the public in the first place.
When the (designed to be long-lasting) n1-methyl pseudouridine modified mRNA transfects one's cells, and gives instructions for the ribosomes to make & express foreign non-self proteins (such as the toxic SARS-CoV-2 spike protein), one's immune system sends the CD8+ cytotoxic T lymphocytes (CTLs) to kill those formerly healthy cells that are now making & expressing non-self proteins.
It is the mission of these CD8+ CTLs to seek out and destroy any such transfected cell that is making foreign non-self proteins. That’s what they do…
Due to the biodistribution properties of the lipid nanoparticles, the encased modified mRNA can go anywhere in the body, including crossing the blood-brain and placental barriers...The LNP "delivery vehicles" traveled to different parts of the body in different people.
Expressing any foreign protein is fatal to the cell doing the expressing. The reason is, our bodies are protected by being able to distinguish ourselves from things that shouldn't be there. Anything non-self will trigger immune destruction of the cells & tissues involved.
Some people will express lots of foreign proteins in vulnerable locations. Others express less in less vulnerable areas.
The location of expression defines the adverse event: if you get foreign protein expression in your heart cells, you could get myocarditis & experience cardiac arrest; if the expression is in your brain, spinal cord, or peripheral nervous system, you could get one or more of a variety of neurological conditions; if in your eye, possible blindness; if in your ovaries, possible infertility; if in the placenta, possible miscarriage, stillbirth, or birth defects; if in the endothelial cells that line your blood vessels, possible vascular &/or microvascular injuries like clots/microclots or the long white fibrous clots, leading to strokes, heart attacks, or pulmonary embolisms…
If the expression of foreign proteins is in your own immune cells, you could experience immune dysfunction, dysregulation, & suppression including repeated infections, immune tolerance of a pathogenic foreign protein due to antibody subclass switch to IgG4 & increased IgG4-related diseases, T cell exhaustion, interference with & suppression of innate immunity, persistent systemic inflammation, dysregulation of toll-like receptors and reduced cancer surveillance or the suppression of tumor-suppressing immune system activities & cell-signaling (increasing your risk of fast-growing and aggressive cancers)…
And more…
There's no limit to the horrible consequences of injecting into your body something that triggers your own immune system to attack & kill your own formerly healthy cells & tissues.
The public “health” agencies, the COVID “authorities”, & the “mainstream” media fraudulently marketed these experimental mRNA gene “therapy” products as “safe & effective vaccines”. Trusting people thought that they were being presented with the choice (or the mandate) as to whether or not to take a “safe & effective vaccine”…But that was/is a deceptively false “choice”…
The COVID-19 mRNA injections are NOT safe, they are NOT effective, and they are NOT vaccines.
These modified mRNA-LNP gene “therapy” injections never would have passed proper safety studies required for gene therapy products. Safety studies (including biodistribution, immunogenicity, immunotoxicity, genotoxicity, carcinogenicity, reproductive toxicity, shedding, long-term effects, & more) that were bypassed because of the fraudulent mislabeling as “vaccines”. (And because of the EUA & “countermeasure” designations under the Project BioShield Act & PREP Act).
NO ONE should have ever had the “choice” of taking these gene “therapy” injections because the modified mRNA-LNP genetic technology platform is fundamentally flawed & dangerous by design.
The danger is NOT limited to just getting more COVID “boosters”. ANY mRNA gene “therapy” product that transfects your cells and instructs those cells to produce foreign non-self proteins (ANY non-self protein) will trigger an immune system attack response against your own cells & tissues (the role of the Killer T-cells is to monitor ALL the cells of the body, ready to destroy/kill any that express foreign, non-self proteins). This makes EVERY mRNA-based injected product harmful by design.
No one who took these modified mRNA-LNP COVID injections made an informed decision. Most people had no clue about what they allowed to be injected into their bodies...
Also most people still do not understand that the devastating harms inflicted upon people over the last few years was intentional:
AFTER the mighty CD8+ Cytotoxic T Lymphocyte cells (AKA Killer T-cells) attack response to modified mRNA transfected cells of tissues & organs inside your body:
After the primary immune system attack response by the cytotoxic T lymphocytes (CTLs), resulting in varying degrees of tissue damage & pathology in different people, a lot happens...
The CTLs will not be able to kill every cell making non-self (spike) protein, so some amount of foreign (spike) protein will get made & released from your cells. That amount will also vary from person to person.
Specialized cells called antigen-presenting cells, especially dendritic cells and macrophages, spring into action. Long story short…you will get serum antibodies made against those foreign proteins which is the stated goal of any shot called a vaccine.
But that can take up to 2 weeks, and during that time, the foreign non-self (spike) proteins are biologically active and will attach to various cellular receptors, resulting in a whole new level of possible tissue destruction.
Now your immune system will activate macrophages & neutrophils that will kill THOSE cells through inflammatory pathways, regardless of whether or not the non-self proteins are toxic themselves.
And if the non-self proteins ARE toxic, like the pathogenic spike proteins, they can cause problems like tissue damage all by themselves without your immune system even being involved at that point.
But your adaptive immune system has done its job & you've made your serum antibodies by now! Yippee!
Too bad those (non-neutralizing, leaky) serum antibodies can only REACT to a (SARS-CoV-2) infection...it is biologically impossible for serum antibodies (in the blood) to PREVENT respiratory infections that enter the body through the mucosa of the mouth/throat, nose, & eyes.
To PREVENT respiratory infections requires a strong innate immune system with mucosal immunity and secretory IgA to stop the respiratory infection at the mucosal and epithelial barriers (stopping the infection OUTSIDE your body and PREVENTING the infection from getting INSIDE your body).
And this is also where the CTLs are supposed to do their cell-destroying activities. When epithelial cells in the mouth/throat, nose, & eyes are infected (like can happen with respiratory diseases) the Killer T-cells will kill those infected cells.
Epithelial cells at the epithelial barrier can be quickly replaced, usually in just a few days in most people. But injections bypass your body's natural protections and send their payload into your body, where that payload can enter your lymph system and bloodstream.
And in the case of the modified mRNA-LNP gene "therapy" injections, this can be disastrous, starting with the immune system attack response against transfected cells of tissues & organs (INSIDE your body) that are now making foreign non-self proteins.
Replacing cells from now damaged tissues and organs inside your body is a complex process that can take weeks or longer, with some areas unable to be repaired at all.
The modification of natural mRNA with synthetic n1-methyl pseudouridine made the modified mRNA longer lasting and resistant to the body’s natural breakdown processes. A Nobel Prize was awarded specifically for this use of longer lasting pseudouridine in the COVID modified mRNA injections.
The synthetic pseudouridine modified mRNA is causing a +1 ribosomal frameshift, as well as a reverse reading, so some people may make spike proteins AND mystery (or junk) non-self proteins.
Studies have found that an antibody subclass switch to IgG4 can occur between mRNA shot #2 & #3, which is sending a stand-down signal to the immune system, essentially telling the immune system to tolerate and ignore the (toxic pathogenic) spike proteins instead of actively fighting to clear the spike from the body.
And people who are getting "booster" after "booster" are repeatedly triggering these immune system activities and causing persistent systemic inflammation, which can cause hyper-immune and autoimmune responses...and then possible immune system exhaustion as your immune system becomes overwhelmed.
Pathology reports, including from autopsies, have revealed & confirmed the Killer T Lymphocyte infiltration & destruction of cells, oftentimes in vital organs.
And then there's the plasmid DNA contamination (with the oncogenic SV-40 promotor sequence) that's been discovered. There are a number of ways in which integration into the human genome is possible...
And more...
Currently, there are more than 5,000 peer-reviewed studies/articles documenting the harms and deaths from the COVID modified mRNA-LNP shots.
This link is to a compilation of over 700 of those peer-reviewed studies & scientific papers:
Tragically, the injuries, disabilities, and deaths from these modified mRNA-LNP gene “therapy” injections prove that the COVID shots have been an IMMUNOLOGICAL CATASTROPHE.
Even more tragically, because more people do not understand that this is not about "choice", this is not about the ability to tell others what to do or not...
Because more people are not standing up and demanding that these "traditional" modified mRNA-LNP transfection injections be pulled from the market, the next "evolution" is moving forward (the self amplifying mRNA technology platform)...
Vioxx, 1976 Swine flu shot, Thalidomide, DES, DDT, etc...etc...ALL removed from the market after having previously been approved for use in the USA, or Europe, or wherever...yet now some people are acting like removing a product from the market is unprecedented...
Dangerous, injurious, deadly products must be pulled from the market!!! You do NOT give uninformed or misinformed people the "choice" to use such products.
Especially when their uninformed "consent" leads to them taking a product that sheds and poses a legitimate danger to the health of those being shed on.
Wang…. Hmm.. are you like one of those Wuhan lab test subjects who just now was able to escape?? Or maybe you’re being racist and poking fun at how black people say “Chicken wangs”??
The point that I object to most in Pioter Cullis’ talk is that he mentions Katelin Kariko’s name far less than himself or Weissman. He does not list her name in his acknowledgements which he reads off. That tells me he is an asshole right there. How you come to your conclusions baffles me. Nothing in his quick summary of his work finding the right self-constructing lipid bubbles can possibly aid you to criticize clear cut elegant medical science. All these separate processes were already present for 45 years but his team but them together. I’m not going to refute the various errors in your understanding but i know that you are not a student of these various areas of cellular biology.
Wow, once again, you have NOT replied under one of my comments...once again, that means I did not receive a notification from substack...it's just pure chance that I rechecked the comment section for this article.
For someone as trained as you keep claiming you are, you sure are afraid of directly responding to me.
Your "clear cut elegant medical science" is inherently flawed and dangerous. The proof of that is in the clear histopathological evidence from biopsies and autopsies.
But acknowledging the histopathological evidence would mean that YOU got this wrong, and your ego certainly won't allow that...
Because that would mean that the grave errors in YOUR understanding of the mRNA transfection platform have jeopardized your health and life...
Since you clearly have no intention of opening your eyes or mind to real facts and the truth about the mRNA transfection injections, I will not waste any more of my valuable time.
That statement is the sole problem with what you say. I’m with you until you contradict the very principles you declare about immunology. I am trained. Maybe that’s my problem?
"One of the other key (hazardous) characteristics of the lipid nanoparticle (LNP) delivery platform is what mainstream media has innocuously called ‘tiny fat bubbles’.
This is a ridiculous simplistic characterization, but one that serves its intended purpose: it’s a dumbed-down cartoon that misinforms the public (as an aside: the media coverage on this has more in common with a sales brochure than a source of reliable information).
The LNP is, more accurately, a cationic lipid; that is, a positively charged lipid particle. What is nearly always excluded from discussion is the reality that only neutral and negatively charged lipids are found in nature. There are no permanently positively charged lipids found in nature. Zero.
It is absolutely unnatural.
As one might expect, this makes cationic lipids incredibly toxic, immunogenic, and inherently unstable.
Polyethylene glycol (PEG) was included as a constituent in formulating the COVID injectable LNPs, which garnered concerns due to the immunogenicity of PEG. But this too is missing the forest for the trees; because, even if one were to remove the PEG from the formulation, the LNP would still be toxic, because it remains, a cationic lipid.
That is a huge omission, even criminal.
The dangers were known.
Further, despite assurances, the LNP’s cannot be targeted in the body. They travel everywhere. They tend to accumulate in the liver, but this is mostly because that is where lipids in circulation are processed normally.
We didn’t actually need the Japanese biodistribution study (https://phmpt.org/wp-content/uploads/2022/03/125742_S1_M4_4223_185350.pdf) to know that the LNP behaved this way. The Platform Mechanics have known about this failing for a very long time. It’s clear that, very early on, there was a choice made not to publicize this important hazard.
Watch this clip of Pieter Cullis, co-founder of Acuitas (https://www.youtube.com/watch?v=qZYa7SGz87U&t=2703s) —the company that developed the LNP technology used in the COVID mRNA shots—where he casually admits that uncontrolled biodistribution is a known phenomenon. Note: Cullis’ PhD is actually in solid state physics and he did not begin attempting to apply his research into nuclear magnetic resonance to biological membranes until his post-doctoral work."
In this clip, Pieter Cullis also casually says:
"It's not like you're inducing production of a protein forever...If you're causing nasty side effects, then ok, stop giving it."
Again, since you don't seem to have read any of the links that I have included, from the link:
"Transfection is the process of artificially introducing nucleic acids (DNA / RNA) into eukaryotic cells by ‘non-viral’ methods.2 It’s actually as inelegant as it sounds. It is, quite literally, hacking cells to make a protein product it naturally would not; specifically, in the case of the COVID injectables (according to the manufacturer’s product literature), the non-self spike protein.
Transfection is like brute-force hacking: literally breaking open the cell wall and inserting a payload. It’s worth considering that it might actually have more in common with impersonation and spycraft than healing. The platform is, by design, at odds with, and trying to deceive the immune system.
Consider just these two questions:
Why is a lipid nanoparticle capsule needed in the first place?
The lipid capsule is the delivery mechanism, but it is first a camouflage strategy for avoiding detection by the immune system and fooling the body into thinking it is just a common natural lipid, like cholesterol. We know that mRNA is intrinsically unstable and quickly degraded due to the omnipresence of RNases in the serum and plasma.3 Breakdown of RNA is an ancient and fundamental process. RNase, or ribonuclease, is a catalyst responsible for the degradation of RNA. Free extracellular RNA is a danger signal to the immune system.
Why was N1-methylpseudouridine used?
All of the uracil nucleosides were systemically replaced with synthetic N1-methyl-pseudouridine. This is another strategy of deception, intended to trick the immune system. Foreign RNA is intrinsically immunogenic—it triggers the immune system. By incorporating synthetic pseudouridine, the T-cell response and activation of Toll-like receptors is suppressed, thus making the mRNA more persistent and less likely to be destroyed by the immune system.4
These two items point to something intuitive and straightforward that laypeople can hold onto: the platform is designed to do something the immune system does not want. Thus, the platform must, by design, impersonate, deceive, and strive to trick the immune system.
The human body doesn’t want foreign genetic material in the bloodstream, and cells don’t want to have foreign genetic material inside the cell wall, yet this is the basis of design for the entire platform. It is attempting to deceive and undermine one of the primary functions of the immune system: recognition of Self vs Non-self.
How does the immune system react to this hacking?
It leaps into action. Inflammation, cellular damage, scarification, apoptosis, genetic damage, cancer, autoimmunity, and more. Cells expressing a foreign protein will be attacked by the immune system and destroyed by T-lymphocytes, apoptosis, and potentially other mechanisms.
What we are learning (the hard way), is that the immune system (and biology in general) is far more complex than the hackers understand. Let’s call these hackers the Platform Mechanics, since they like to regard the immune system as a relatively simplistic machine that they are able to tweak and manipulate.
Now, a simple mechanical hack can work for McGyver on TV because, typically, there’s a simple physical mechanism at play, like a slingshot or a lever. Hacking the human body, however—especially aspects and systems incorporating genetic information (that we only dimly understand)—will foreseeably end up being an exercise in recklessness. And an expensive one, paid in lives.
The Platform Mechanics want you to believe in the ‘genius’ of ‘progress’ and marvel at how they’re able to hack biology. But it’s all a fantasy (or rather, a horror movie). They don’t really understand what they are doing, or the long term impacts, but they want you to believe they do."
You’ve done a remarkable job self-educating yourself about this. It’s still a work in progress with some fundamental misconceptions, ie, foreign non-self proteins. Your argument appears sophisticated but it’s not really. Sorry immunology is very complex. Get a degree in the field. You could be great at it
"While the pharmaceutical industry rushes to expand mRNA use for its speed and profit, a fundamental immunological principle is being overlooked: Any cell that produces a foreign protein is marked for destruction by the immune system.
This isn't theoretical. Clear histopathological evidence from biopsies and autopsies confirms the vaccine's genetic material does not stay at the injection site. It enters systemic circulation and spreads uncontrollably throughout the body, including to vital organs like the brain and heart.
Once there, the body's own cells are forced to produce the foreign antigen, triggering an immune attack on its own tissues."
EVERY SINGLE DOCTOR and medical professional should have been able to recognize that the mRNA transfection platform would trigger this immune attack on the body's own cells and tissues.
You are the one who is espousing fundamental misconceptions about immunology and these mRNA injections.
For your own sake, I sincerely hope you take the time to educate and inform yourself about the inherent dangers of the mRNA transfection platform.
It should infuriate every American that our President just wined and dinned the Big Pharma Snake Bourla at our White House, praised him for doing such a good job on the mRNA poison and gave him BILLIONS more tax payer dollars for MORE POISON. They are just poking us in the eye, this is pure evil.
IMHO - While the binary question of toxin versus not, seems to flip a legal switch on whether this is a bioweapon, that’s not logical. We need to remember that all drugs are toxic (with an R factor) because they are patented, manmade, exogenous factors and function neither within a normal biological range of chemistry nor natural in its ingredients.
Is the dispositive point for the court that the quality control on such toxic products as a pharmaceutical product like these shots needs to be identified and confirmed by the regulatory authorities based on suppliers’ test data, but was not? Rather, our US regulators colluded with suppliers to distribute toxic products for profit, without upholding their responsibility for protecting public safety. Can we call it reckless disregard, willful negligence and racketeering?
If you want to see my years of research on the COVID "vaccine" bioweapon including spiritual connections, gematria, and links to scientific results and more. go to:
www.kimpaddock.com
Hard to get excited after 11 states had similar bills that all fizzled!
Well, none of them had bills that said the shots were already illegal according to existing bioweapons or weapons of mass destruction laws and created a criminal and civil liability for non enforcement. The point is to get it introduced in as many places as possible to create pressure.
I get your point. This rabbit hole goes deep, does it not?
On the surface, we were told that Operation WARp SpEED was a success...
Then, we have reality: DARPA was working on mRNA technology for SARS-CoV-2 in 2012 through the Adept program!
The point: The narrative NEVER matches reality!
Be blessed!
Thank you Dr.Joe for your continued efforts.
Why dr Joe, you are being over the world known now, quite impressive for a one person show and agit. But you and a few more people, like Ana and Karen, certainly merit all the attention y ou get these days. One only wonders, w hat took t he rest of the world so long? The facts have been t here open for all to see, so no eyes? no brains? no guts? or what are these people missing?
I know. We are not winning. We need to keep the pressure on.
International Tribunal Declares COVID mRNA Injections 'Biological and Technological Weapons of Mass Destruction' International Tribunal Declares COVID mRNA Injections 'Biological Weapons of Mass Destruction. Dr. Joseph Sansone explains the first international judicial declaration labelling mRNA vaccines as bioweapons.
DEADLY Covid mRNA injections are, at last, formally declared and certified by a 'Sovereign Nation', as 'Bioweapons of Mass Destruction'!
At long last, the truth, reality and common sense are beginning to surface!
Big Pharma can't hide this depopulation Plan for much longer. They will have to relinquish their 'PREP Act' shield to prosecution for causing masses of 'VAX' injuries and VAX-related DEATHS.
Unjabbed Mick (UK Patriot) We live longer!
This is total batshit crazy mis-information. The author is a crazy therapist of dubious value way out of his lane. This channel is facilitating false information about vaccines which are the pinnacle of medical science. Why do people attack phenomenal things? A case in point: why was Caitlin Clark assaulted by her fellow basketball players for the past 2 years. An exceptional basketball player, an exceptional vaccination with irrational illogical violent attackers. Senseless, useless, harmful
VAX vs UNVAX Study
https://theylied.substack.com/p/theylied-vax-vs-unvax-study-and-documentary
.
Did you take your tenth covid booster yet?
Touche' ;)
I wish. I’m about to get one . Thanks for asking. Substantially less chances for COVID-19, long sequelae, susceptibility to other illnesses like MIs, CVAs, HTN, DM and CHF. Pus being sick and out of commission is not my cup of tea. Basically I’ve never seen or heard of a vaccine that I didn’t want. I wish I could get several vaccines that I’m not eligible for.
We wish you all the best. Have a great day.
Right? To become a walking bioweapon oneself who's shedding all those toxins on those in proximity has to be the absolute mark of a moron who in wishing they could get MORE "vaccines" wonders why they keep getting sick. You have to wonder how they made it this far in life. The gatekeepers in these comments floor me.
Colby Wang, you have been horribly misinformed and misled.
More people need to understand that it is not enough for there to be no mandates...
The modified mRNA-LNP gene "therapy" transfection injections are dangerous by design.
And they can shed on others, making them dangerous for those who said "Hell NO!" as well...
Self vs Non-self is basic foundational Immunology 101...But the mRNA shots undermine this essential principle.
The mRNA shots were/are always going to be an immunological catastrophe for humanity.
The mechanism of action (using mRNA instructions to turn one’s own cells into foreign non-self “spike protein factories”) is the primary mechanism of harm.
The primary danger of the COVID-19 mRNA injections has always been one’s own immune system’s attack response by the mighty CD8+ Cytotoxic T Lymphocyte cells (AKA Killer T-cells):
The COVID-19 mRNA injections must be recalled from the market and mRNA-based products must be banned because the modified mRNA-LNP genetic technology platform is fundamentally flawed & dangerous by design.
These modified mRNA-LNP COVID-19 injections, that trigger one's own immune system to attack & kill one's own formerly healthy cells (that have been instructed to produce/express foreign, non-self proteins), no matter where those cells are in the body, never should have been made available to the public in the first place.
When the (designed to be long-lasting) n1-methyl pseudouridine modified mRNA transfects one's cells, and gives instructions for the ribosomes to make & express foreign non-self proteins (such as the toxic SARS-CoV-2 spike protein), one's immune system sends the CD8+ cytotoxic T lymphocytes (CTLs) to kill those formerly healthy cells that are now making & expressing non-self proteins.
It is the mission of these CD8+ CTLs to seek out and destroy any such transfected cell that is making foreign non-self proteins. That’s what they do…
Due to the biodistribution properties of the lipid nanoparticles, the encased modified mRNA can go anywhere in the body, including crossing the blood-brain and placental barriers...The LNP "delivery vehicles" traveled to different parts of the body in different people.
Expressing any foreign protein is fatal to the cell doing the expressing. The reason is, our bodies are protected by being able to distinguish ourselves from things that shouldn't be there. Anything non-self will trigger immune destruction of the cells & tissues involved.
Some people will express lots of foreign proteins in vulnerable locations. Others express less in less vulnerable areas.
The location of expression defines the adverse event: if you get foreign protein expression in your heart cells, you could get myocarditis & experience cardiac arrest; if the expression is in your brain, spinal cord, or peripheral nervous system, you could get one or more of a variety of neurological conditions; if in your eye, possible blindness; if in your ovaries, possible infertility; if in the placenta, possible miscarriage, stillbirth, or birth defects; if in the endothelial cells that line your blood vessels, possible vascular &/or microvascular injuries like clots/microclots or the long white fibrous clots, leading to strokes, heart attacks, or pulmonary embolisms…
If the expression of foreign proteins is in your own immune cells, you could experience immune dysfunction, dysregulation, & suppression including repeated infections, immune tolerance of a pathogenic foreign protein due to antibody subclass switch to IgG4 & increased IgG4-related diseases, T cell exhaustion, interference with & suppression of innate immunity, persistent systemic inflammation, dysregulation of toll-like receptors and reduced cancer surveillance or the suppression of tumor-suppressing immune system activities & cell-signaling (increasing your risk of fast-growing and aggressive cancers)…
And more…
There's no limit to the horrible consequences of injecting into your body something that triggers your own immune system to attack & kill your own formerly healthy cells & tissues.
The public “health” agencies, the COVID “authorities”, & the “mainstream” media fraudulently marketed these experimental mRNA gene “therapy” products as “safe & effective vaccines”. Trusting people thought that they were being presented with the choice (or the mandate) as to whether or not to take a “safe & effective vaccine”…But that was/is a deceptively false “choice”…
The COVID-19 mRNA injections are NOT safe, they are NOT effective, and they are NOT vaccines.
These modified mRNA-LNP gene “therapy” injections never would have passed proper safety studies required for gene therapy products. Safety studies (including biodistribution, immunogenicity, immunotoxicity, genotoxicity, carcinogenicity, reproductive toxicity, shedding, long-term effects, & more) that were bypassed because of the fraudulent mislabeling as “vaccines”. (And because of the EUA & “countermeasure” designations under the Project BioShield Act & PREP Act).
NO ONE should have ever had the “choice” of taking these gene “therapy” injections because the modified mRNA-LNP genetic technology platform is fundamentally flawed & dangerous by design.
The danger is NOT limited to just getting more COVID “boosters”. ANY mRNA gene “therapy” product that transfects your cells and instructs those cells to produce foreign non-self proteins (ANY non-self protein) will trigger an immune system attack response against your own cells & tissues (the role of the Killer T-cells is to monitor ALL the cells of the body, ready to destroy/kill any that express foreign, non-self proteins). This makes EVERY mRNA-based injected product harmful by design.
No one who took these modified mRNA-LNP COVID injections made an informed decision. Most people had no clue about what they allowed to be injected into their bodies...
Also most people still do not understand that the devastating harms inflicted upon people over the last few years was intentional:
https://rumble.com/v6qcb0y-dr.-david-martin-mar-06-2025-edmonton-alberta-replay.html
Part 2
AFTER the mighty CD8+ Cytotoxic T Lymphocyte cells (AKA Killer T-cells) attack response to modified mRNA transfected cells of tissues & organs inside your body:
After the primary immune system attack response by the cytotoxic T lymphocytes (CTLs), resulting in varying degrees of tissue damage & pathology in different people, a lot happens...
The CTLs will not be able to kill every cell making non-self (spike) protein, so some amount of foreign (spike) protein will get made & released from your cells. That amount will also vary from person to person.
Specialized cells called antigen-presenting cells, especially dendritic cells and macrophages, spring into action. Long story short…you will get serum antibodies made against those foreign proteins which is the stated goal of any shot called a vaccine.
But that can take up to 2 weeks, and during that time, the foreign non-self (spike) proteins are biologically active and will attach to various cellular receptors, resulting in a whole new level of possible tissue destruction.
Now your immune system will activate macrophages & neutrophils that will kill THOSE cells through inflammatory pathways, regardless of whether or not the non-self proteins are toxic themselves.
And if the non-self proteins ARE toxic, like the pathogenic spike proteins, they can cause problems like tissue damage all by themselves without your immune system even being involved at that point.
But your adaptive immune system has done its job & you've made your serum antibodies by now! Yippee!
Too bad those (non-neutralizing, leaky) serum antibodies can only REACT to a (SARS-CoV-2) infection...it is biologically impossible for serum antibodies (in the blood) to PREVENT respiratory infections that enter the body through the mucosa of the mouth/throat, nose, & eyes.
To PREVENT respiratory infections requires a strong innate immune system with mucosal immunity and secretory IgA to stop the respiratory infection at the mucosal and epithelial barriers (stopping the infection OUTSIDE your body and PREVENTING the infection from getting INSIDE your body).
And this is also where the CTLs are supposed to do their cell-destroying activities. When epithelial cells in the mouth/throat, nose, & eyes are infected (like can happen with respiratory diseases) the Killer T-cells will kill those infected cells.
Epithelial cells at the epithelial barrier can be quickly replaced, usually in just a few days in most people. But injections bypass your body's natural protections and send their payload into your body, where that payload can enter your lymph system and bloodstream.
And in the case of the modified mRNA-LNP gene "therapy" injections, this can be disastrous, starting with the immune system attack response against transfected cells of tissues & organs (INSIDE your body) that are now making foreign non-self proteins.
Replacing cells from now damaged tissues and organs inside your body is a complex process that can take weeks or longer, with some areas unable to be repaired at all.
The modification of natural mRNA with synthetic n1-methyl pseudouridine made the modified mRNA longer lasting and resistant to the body’s natural breakdown processes. A Nobel Prize was awarded specifically for this use of longer lasting pseudouridine in the COVID modified mRNA injections.
The synthetic pseudouridine modified mRNA is causing a +1 ribosomal frameshift, as well as a reverse reading, so some people may make spike proteins AND mystery (or junk) non-self proteins.
Studies have found that an antibody subclass switch to IgG4 can occur between mRNA shot #2 & #3, which is sending a stand-down signal to the immune system, essentially telling the immune system to tolerate and ignore the (toxic pathogenic) spike proteins instead of actively fighting to clear the spike from the body.
And people who are getting "booster" after "booster" are repeatedly triggering these immune system activities and causing persistent systemic inflammation, which can cause hyper-immune and autoimmune responses...and then possible immune system exhaustion as your immune system becomes overwhelmed.
Pathology reports, including from autopsies, have revealed & confirmed the Killer T Lymphocyte infiltration & destruction of cells, oftentimes in vital organs.
And then there's the plasmid DNA contamination (with the oncogenic SV-40 promotor sequence) that's been discovered. There are a number of ways in which integration into the human genome is possible...
And more...
Currently, there are more than 5,000 peer-reviewed studies/articles documenting the harms and deaths from the COVID modified mRNA-LNP shots.
This link is to a compilation of over 700 of those peer-reviewed studies & scientific papers:
https://zenodo.org/records/15787612
Tragically, the injuries, disabilities, and deaths from these modified mRNA-LNP gene “therapy” injections prove that the COVID shots have been an IMMUNOLOGICAL CATASTROPHE.
Even more tragically, because more people do not understand that this is not about "choice", this is not about the ability to tell others what to do or not...
Because more people are not standing up and demanding that these "traditional" modified mRNA-LNP transfection injections be pulled from the market, the next "evolution" is moving forward (the self amplifying mRNA technology platform)...
https://www.drtrozzi.news/p/world-council-for-health-the-dangers
Vioxx, 1976 Swine flu shot, Thalidomide, DES, DDT, etc...etc...ALL removed from the market after having previously been approved for use in the USA, or Europe, or wherever...yet now some people are acting like removing a product from the market is unprecedented...
Dangerous, injurious, deadly products must be pulled from the market!!! You do NOT give uninformed or misinformed people the "choice" to use such products.
Especially when their uninformed "consent" leads to them taking a product that sheds and poses a legitimate danger to the health of those being shed on.
https://www.midwesterndoctor.com/p/what-weve-learned-from-a-year-of
https://pierrekorymedicalmusings.com/p/shedding-of-covid-mrna-vaccine-components
(This is part 1 of a 9 part series - other parts linked at the end of the part 1 article)...
I cannot say it enough: It is NOT enough for there to be no mandates.
"This does present a very serious risk to the survival of our species"...
https://www.drtrozzi.news/p/the-harms-and-mechanisms-of-the-covid
"The failure and dangers of these genetic experiments, they were predictable, based on scientific knowledge that preceded 2020"...
👏🏼👏🏼👏🏼❤️
Enjoy…. Enjoy all you can get. Maybe even take three a day.
I think this is either a paid troll or a bot. I can’t imagine any real, serious person still being so misinformed and lashing out in such a way.
Wang…. Hmm.. are you like one of those Wuhan lab test subjects who just now was able to escape?? Or maybe you’re being racist and poking fun at how black people say “Chicken wangs”??
The point that I object to most in Pioter Cullis’ talk is that he mentions Katelin Kariko’s name far less than himself or Weissman. He does not list her name in his acknowledgements which he reads off. That tells me he is an asshole right there. How you come to your conclusions baffles me. Nothing in his quick summary of his work finding the right self-constructing lipid bubbles can possibly aid you to criticize clear cut elegant medical science. All these separate processes were already present for 45 years but his team but them together. I’m not going to refute the various errors in your understanding but i know that you are not a student of these various areas of cellular biology.
Wow, once again, you have NOT replied under one of my comments...once again, that means I did not receive a notification from substack...it's just pure chance that I rechecked the comment section for this article.
For someone as trained as you keep claiming you are, you sure are afraid of directly responding to me.
Your "clear cut elegant medical science" is inherently flawed and dangerous. The proof of that is in the clear histopathological evidence from biopsies and autopsies.
But acknowledging the histopathological evidence would mean that YOU got this wrong, and your ego certainly won't allow that...
Because that would mean that the grave errors in YOUR understanding of the mRNA transfection platform have jeopardized your health and life...
Since you clearly have no intention of opening your eyes or mind to real facts and the truth about the mRNA transfection injections, I will not waste any more of my valuable time.
That statement is the sole problem with what you say. I’m with you until you contradict the very principles you declare about immunology. I am trained. Maybe that’s my problem?
I have NOT contradicted the very principles I have declared about immunology.
Your current understanding of the modified mRNA-LNP transfection injections and the mRNA transfection platform is horribly misinformed.
Please actually look at the links I have included. Or does all your training mean that you have nothing more to learn??
And why do you keep trying to hide your comments from me?
Several of your comments have been clearly addressing what I have written, and yet you keep posting your comments (to me) under your own comments.
In the future, if you want to continue this exchange, please actually reply to one of my comments so that I receive the notification from substack...
site. It enters systemic circulation and spreads uncontrollably throughout the body, including to vital organs like the brain and heart.”
The lipid nanoparticles achieve widespread biodistribution. This is NOT theoretical.
Since you don't seem to want to look at or read any of the links that I've previously included, let me highlight a passage that is in this link:
https://entwine.substack.com/p/the-platform-is-deadly
"One of the other key (hazardous) characteristics of the lipid nanoparticle (LNP) delivery platform is what mainstream media has innocuously called ‘tiny fat bubbles’.
This is a ridiculous simplistic characterization, but one that serves its intended purpose: it’s a dumbed-down cartoon that misinforms the public (as an aside: the media coverage on this has more in common with a sales brochure than a source of reliable information).
The LNP is, more accurately, a cationic lipid; that is, a positively charged lipid particle. What is nearly always excluded from discussion is the reality that only neutral and negatively charged lipids are found in nature. There are no permanently positively charged lipids found in nature. Zero.
It is absolutely unnatural.
As one might expect, this makes cationic lipids incredibly toxic, immunogenic, and inherently unstable.
Polyethylene glycol (PEG) was included as a constituent in formulating the COVID injectable LNPs, which garnered concerns due to the immunogenicity of PEG. But this too is missing the forest for the trees; because, even if one were to remove the PEG from the formulation, the LNP would still be toxic, because it remains, a cationic lipid.
That is a huge omission, even criminal.
The dangers were known.
Further, despite assurances, the LNP’s cannot be targeted in the body. They travel everywhere. They tend to accumulate in the liver, but this is mostly because that is where lipids in circulation are processed normally.
We didn’t actually need the Japanese biodistribution study (https://phmpt.org/wp-content/uploads/2022/03/125742_S1_M4_4223_185350.pdf) to know that the LNP behaved this way. The Platform Mechanics have known about this failing for a very long time. It’s clear that, very early on, there was a choice made not to publicize this important hazard.
Watch this clip of Pieter Cullis, co-founder of Acuitas (https://www.youtube.com/watch?v=qZYa7SGz87U&t=2703s) —the company that developed the LNP technology used in the COVID mRNA shots—where he casually admits that uncontrolled biodistribution is a known phenomenon. Note: Cullis’ PhD is actually in solid state physics and he did not begin attempting to apply his research into nuclear magnetic resonance to biological membranes until his post-doctoral work."
In this clip, Pieter Cullis also casually says:
"It's not like you're inducing production of a protein forever...If you're causing nasty side effects, then ok, stop giving it."
Again, since you don't seem to have read any of the links that I have included, from the link:
https://entwine.substack.com/p/the-platform-is-deadly
"Transfection is the process of artificially introducing nucleic acids (DNA / RNA) into eukaryotic cells by ‘non-viral’ methods.2 It’s actually as inelegant as it sounds. It is, quite literally, hacking cells to make a protein product it naturally would not; specifically, in the case of the COVID injectables (according to the manufacturer’s product literature), the non-self spike protein.
Transfection is like brute-force hacking: literally breaking open the cell wall and inserting a payload. It’s worth considering that it might actually have more in common with impersonation and spycraft than healing. The platform is, by design, at odds with, and trying to deceive the immune system.
Consider just these two questions:
Why is a lipid nanoparticle capsule needed in the first place?
The lipid capsule is the delivery mechanism, but it is first a camouflage strategy for avoiding detection by the immune system and fooling the body into thinking it is just a common natural lipid, like cholesterol. We know that mRNA is intrinsically unstable and quickly degraded due to the omnipresence of RNases in the serum and plasma.3 Breakdown of RNA is an ancient and fundamental process. RNase, or ribonuclease, is a catalyst responsible for the degradation of RNA. Free extracellular RNA is a danger signal to the immune system.
Why was N1-methylpseudouridine used?
All of the uracil nucleosides were systemically replaced with synthetic N1-methyl-pseudouridine. This is another strategy of deception, intended to trick the immune system. Foreign RNA is intrinsically immunogenic—it triggers the immune system. By incorporating synthetic pseudouridine, the T-cell response and activation of Toll-like receptors is suppressed, thus making the mRNA more persistent and less likely to be destroyed by the immune system.4
These two items point to something intuitive and straightforward that laypeople can hold onto: the platform is designed to do something the immune system does not want. Thus, the platform must, by design, impersonate, deceive, and strive to trick the immune system.
The human body doesn’t want foreign genetic material in the bloodstream, and cells don’t want to have foreign genetic material inside the cell wall, yet this is the basis of design for the entire platform. It is attempting to deceive and undermine one of the primary functions of the immune system: recognition of Self vs Non-self.
How does the immune system react to this hacking?
It leaps into action. Inflammation, cellular damage, scarification, apoptosis, genetic damage, cancer, autoimmunity, and more. Cells expressing a foreign protein will be attacked by the immune system and destroyed by T-lymphocytes, apoptosis, and potentially other mechanisms.
What we are learning (the hard way), is that the immune system (and biology in general) is far more complex than the hackers understand. Let’s call these hackers the Platform Mechanics, since they like to regard the immune system as a relatively simplistic machine that they are able to tweak and manipulate.
Now, a simple mechanical hack can work for McGyver on TV because, typically, there’s a simple physical mechanism at play, like a slingshot or a lever. Hacking the human body, however—especially aspects and systems incorporating genetic information (that we only dimly understand)—will foreseeably end up being an exercise in recklessness. And an expensive one, paid in lives.
The Platform Mechanics want you to believe in the ‘genius’ of ‘progress’ and marvel at how they’re able to hack biology. But it’s all a fantasy (or rather, a horror movie). They don’t really understand what they are doing, or the long term impacts, but they want you to believe they do."
You’ve done a remarkable job self-educating yourself about this. It’s still a work in progress with some fundamental misconceptions, ie, foreign non-self proteins. Your argument appears sophisticated but it’s not really. Sorry immunology is very complex. Get a degree in the field. You could be great at it
Did you mean to post this under my comments? Because it appears that you are addressing what I wrote...
Yes, human immunology IS very complex.
But some core principles are basic and foundational, like Self vs Non-self.
https://x.com/newstart_2024/status/1981375686251069797
(approximately 2 min video)
"While the pharmaceutical industry rushes to expand mRNA use for its speed and profit, a fundamental immunological principle is being overlooked: Any cell that produces a foreign protein is marked for destruction by the immune system.
This isn't theoretical. Clear histopathological evidence from biopsies and autopsies confirms the vaccine's genetic material does not stay at the injection site. It enters systemic circulation and spreads uncontrollably throughout the body, including to vital organs like the brain and heart.
Once there, the body's own cells are forced to produce the foreign antigen, triggering an immune attack on its own tissues."
https://entwine.substack.com/p/the-platform-is-deadly
EVERY SINGLE DOCTOR and medical professional should have been able to recognize that the mRNA transfection platform would trigger this immune attack on the body's own cells and tissues.
You are the one who is espousing fundamental misconceptions about immunology and these mRNA injections.
For your own sake, I sincerely hope you take the time to educate and inform yourself about the inherent dangers of the mRNA transfection platform.