Thank you to all the brave doctors & scientists and all the people of the world with curiosity, integrity, and strength of character who have risked so much to get this info out into the world.
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...
I am not a doctor…so PLEASE let me know of any corrections that need to be made if I have misstated something…
But tragically, I think the injuries, disabilities, and deaths from these modified mRNA-LNP gene “therapy” injections prove that the COVID shots have been an IMMUNOLOGICAL CATASTROPHE.
Footnote:
Credit to Dr. Sucharit Bhakdi, Dr. Mike Yeadon, Dr. Kevin Stillwagon, & Dr. Ryan Cole for their videos & articles from which I furthered my understanding of human immunology and the essential component of Self vs. Non-self.
Portions of my 2 comments relied on my notes from their work, as well as other doctors' and scientists' work from my over 10,000 hours researching all things "COVID" and the modified mRNA-LNP gene "therapy" injections since 2020. But as I am not a professional researcher, either, I am sorry to say that I neglected to keep proper citations.
I truly believe this mRNA project might very well be the great deception spoken of in the Bible. It also is looking more and more like part one of the mark of the beast. People don’t like to talk about the spiritual side of global events which gives new understanding to the scripture that says “my people die for lack of knowledge”.
Thanks for all your work and the information you are providing to enlighten your readers. it is unbelievable that the providers of these vile products continue to push them on people with the blessings of governments worldwide. They should have been removed from the market at the get-go, after the harm they were doing was known. It definitely has to be part of the NWO Agenda to eliminate as much of the population as possible.
hmmm. "definitely has to be part of the NWO Agenda. . ."
or, simply greedy bureaucrats protecting turf. Being the #1 superpower in the entire world, it is hard for me to agree that the entire "deep state" has been leveraged against the entire USA.
On the other hand, where the hell are the whistle-blowers?
Thank you for your continued work at exposing this depopulation scheme. So glad I didnt get coerced into taking that poison. And too bad our captured media wouldn't report this, and convince people to detox, and quit taking boosters!. Gates, Collins, Daszak and Fauci should all be sharing a jail cell.
Thank you Dr. Catanzaro, my immunology professor was from U of North Texas out of the osteopathic school in Fort Worth. Kudos to her , she discussed a similar mechanism, but it may have been all theory . The MRNA technology was so new back then and she told us to never be a part of it . I am grateful to her , this caused me not to take the jab and get a religious exemption.
Way too much confusing terminology and cellular level detail with no basic biology or honest summary that human bodies NEVER tolerate non-self proteins and disaster was entirely predictable from 1999 Biotech Death of Jesse Gelsinger.
Spike fragments may contribute but EVERY non-self protein produced will trigger immune system attack of affected cells and LNP uncontrolled distribution a guarantee it will go everywhere. None of this is new or surprising and calling it a vaccine adds to fraud.
TRANSFECTION is decades old lab tool where CRISPR clones are grown in E.coli and stuffed into rodents to produce models for vaccine development. ALL these lab produced clones are Gain of Function experiments that have been distorted to a mythology that petrie dish clones can be released and replicate with fidelity in the air and cause a pandemic which is as close to reality as Cat in the Hat pink snow.
In the Gardener Prize tour pre-Nobel Prize for lobotomy level LNP Pieter Cullis lifelong LNP researcher seeking an alternative drug delivery for chemotherapy that hits less than 1% of targeted cells this uncontrolled LNP was confirmed. Anybody who is honest & informed calls these mRNA TRANSFECTION and knows it's deadly by design with ZERO biological mechanisms to usefully augment the immune system.
Start speaking truth & learn the biology. TRANSFECTING people is criminal.
Not sure why anyone expects Gates WHO Biotech Mafia to undermine their profit schemes but MDs pretending to be advocates for human health is another matter.
Everyone calling mRNA TRANSFECTION a vaccine is dishonest there are countless references in Robert Malone's old CV before Covidian fraud and my name has six letters not three thanks! Pamela :~)
I hope to see ongoing discussion of how we understand the immune system responses to the Covid virus, and the Covid-Vax agents (spikes, etc.), are distinguishable from:
"classic" auto-immune mechanics of "auto-immune" illnesses. (as we now understand them)
"... it was hypothesized that, various categories of polyphenolic compounds may exert comparable antiviral activities while involving different mechanisms of action. Based on this hypothesis, it was of great importance to scrutinize the antiviral activity of the natural polyphenolic Cuphea ignea extract, instead of the single purified compounds. According to these results, it is suggested that the intriguing antiviral activity of the extract and the formulation may be attributed to a possible synergism between the extract components." - Delineating a potent antiviral activity of Cuphea ignea extract loaded nano-formulation against SARS-CoV-2: In silico and in vitro studies Dina B Mahmoud a, et al. - Solution perhaps so no excuse to give clot shot.
I understand Bill Gates is marketing his counterfeit meat in the U.K. for pets. Yet another sneaky use of disease vectors to alter human DNA. If prion ingested can mutate DNA, (and it can), as in CJD, then Gates, again, is using fake science as a cover for his eugenics program... dysregulation linked to cancer and chronic disease. Would someone please put out a wanted poster on this freak is the question I have remaining. Fauci worked for Gates... what a team: straight from hell.
This is all about depopulation. They have stated that their goal is to eliminate 7.5 billion people. That is the majority of people on earth.. Few will be chosen to survive and they will be intensely controlled. This is all about Technocracy, as Pat Wood and David Hughes have stated many times.
I get sinus infections and steady Eustachian tube inflammation, dyspnea, now for 4 years since the second shot. My doctor put me on Singular and cromolyn sodium but it doesn't help. He says well, we're addressing your mast cell dysfunction. But I doubt if deeper down, mast cell disruption is really the problem, but only the expression of systemic inflammation, and so addressing mast cells isn't the answer.
From the beginning, I maintained that, from what I understood about the mechanism for mRNA technology, the individual's genetic make-up would be altered if injected. I also said that each individual is unique; the injections will play quite differently for people; and scientists involved in this "research" had no idea how this technology would truly disrupt the human body. I'm very glad to see verifiable proof now arising.
mRNA is the largest global genocide project in human history imho. Time for Neuremberg 2.0
Thank you to all the brave doctors & scientists and all the people of the world with curiosity, integrity, and strength of character who have risked so much to get this info out into the world.
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...
I am not a doctor…so PLEASE let me know of any corrections that need to be made if I have misstated something…
But tragically, I think the injuries, disabilities, and deaths from these modified mRNA-LNP gene “therapy” injections prove that the COVID shots have been an IMMUNOLOGICAL CATASTROPHE.
Footnote:
Credit to Dr. Sucharit Bhakdi, Dr. Mike Yeadon, Dr. Kevin Stillwagon, & Dr. Ryan Cole for their videos & articles from which I furthered my understanding of human immunology and the essential component of Self vs. Non-self.
Portions of my 2 comments relied on my notes from their work, as well as other doctors' and scientists' work from my over 10,000 hours researching all things "COVID" and the modified mRNA-LNP gene "therapy" injections since 2020. But as I am not a professional researcher, either, I am sorry to say that I neglected to keep proper citations.
I truly believe this mRNA project might very well be the great deception spoken of in the Bible. It also is looking more and more like part one of the mark of the beast. People don’t like to talk about the spiritual side of global events which gives new understanding to the scripture that says “my people die for lack of knowledge”.
Thanks for all your work and the information you are providing to enlighten your readers. it is unbelievable that the providers of these vile products continue to push them on people with the blessings of governments worldwide. They should have been removed from the market at the get-go, after the harm they were doing was known. It definitely has to be part of the NWO Agenda to eliminate as much of the population as possible.
hmmm. "definitely has to be part of the NWO Agenda. . ."
or, simply greedy bureaucrats protecting turf. Being the #1 superpower in the entire world, it is hard for me to agree that the entire "deep state" has been leveraged against the entire USA.
On the other hand, where the hell are the whistle-blowers?
Thank you for your continued work at exposing this depopulation scheme. So glad I didnt get coerced into taking that poison. And too bad our captured media wouldn't report this, and convince people to detox, and quit taking boosters!. Gates, Collins, Daszak and Fauci should all be sharing a jail cell.
Thank you Dr. Catanzaro, my immunology professor was from U of North Texas out of the osteopathic school in Fort Worth. Kudos to her , she discussed a similar mechanism, but it may have been all theory . The MRNA technology was so new back then and she told us to never be a part of it . I am grateful to her , this caused me not to take the jab and get a religious exemption.
Way too much confusing terminology and cellular level detail with no basic biology or honest summary that human bodies NEVER tolerate non-self proteins and disaster was entirely predictable from 1999 Biotech Death of Jesse Gelsinger.
https://web.archive.org/web/20121025034826/https://www.nytimes.com/1999/11/28/magazine/the-biotech-death-of-jesse-gelsinger.html
Spike fragments may contribute but EVERY non-self protein produced will trigger immune system attack of affected cells and LNP uncontrolled distribution a guarantee it will go everywhere. None of this is new or surprising and calling it a vaccine adds to fraud.
TRANSFECTION is decades old lab tool where CRISPR clones are grown in E.coli and stuffed into rodents to produce models for vaccine development. ALL these lab produced clones are Gain of Function experiments that have been distorted to a mythology that petrie dish clones can be released and replicate with fidelity in the air and cause a pandemic which is as close to reality as Cat in the Hat pink snow.
https://web.archive.org/web/20161206155142/http://www.gryphonscientific.com/wp-content/uploads/2016/04/Risk-and-Benefit-Analysis-of-Gain-of-Function-Research-Final-Report.pdf
In the Gardener Prize tour pre-Nobel Prize for lobotomy level LNP Pieter Cullis lifelong LNP researcher seeking an alternative drug delivery for chemotherapy that hits less than 1% of targeted cells this uncontrolled LNP was confirmed. Anybody who is honest & informed calls these mRNA TRANSFECTION and knows it's deadly by design with ZERO biological mechanisms to usefully augment the immune system.
Start speaking truth & learn the biology. TRANSFECTING people is criminal.
https://rumble.com/v3q5vbq-2023-10-17-pieter-cullis-2022-study-hall-16-oct-2023-brief-twitch1953665426.html
WHO is not speaking truth and specifically itemize the lies and transgressions you object to. . .
Not sure why anyone expects Gates WHO Biotech Mafia to undermine their profit schemes but MDs pretending to be advocates for human health is another matter.
Pam, I was referring with the pronoun "who" not the World H. . .
asking for backup refs.
Everyone calling mRNA TRANSFECTION a vaccine is dishonest there are countless references in Robert Malone's old CV before Covidian fraud and my name has six letters not three thanks! Pamela :~)
https://web.archive.org/web/20250718201342/https://www.scirp.org/journal/detailedInforofeditorialboard?personid=5968
I hope to see ongoing discussion of how we understand the immune system responses to the Covid virus, and the Covid-Vax agents (spikes, etc.), are distinguishable from:
"classic" auto-immune mechanics of "auto-immune" illnesses. (as we now understand them)
Thanks, Nic.
You have been lied to about the f00d supply crisis and they are poisoning you watch this…
http://sfood1.trackdok.com
"... it was hypothesized that, various categories of polyphenolic compounds may exert comparable antiviral activities while involving different mechanisms of action. Based on this hypothesis, it was of great importance to scrutinize the antiviral activity of the natural polyphenolic Cuphea ignea extract, instead of the single purified compounds. According to these results, it is suggested that the intriguing antiviral activity of the extract and the formulation may be attributed to a possible synergism between the extract components." - Delineating a potent antiviral activity of Cuphea ignea extract loaded nano-formulation against SARS-CoV-2: In silico and in vitro studies Dina B Mahmoud a, et al. - Solution perhaps so no excuse to give clot shot.
Hey all that "science" has made the world sicker over the last 5 years. What great progress.
I understand Bill Gates is marketing his counterfeit meat in the U.K. for pets. Yet another sneaky use of disease vectors to alter human DNA. If prion ingested can mutate DNA, (and it can), as in CJD, then Gates, again, is using fake science as a cover for his eugenics program... dysregulation linked to cancer and chronic disease. Would someone please put out a wanted poster on this freak is the question I have remaining. Fauci worked for Gates... what a team: straight from hell.
Very sad. I even feel sad for all the nasty people who called me a “superspreader”, killer & so forth because I would not take the jab
This is all about depopulation. They have stated that their goal is to eliminate 7.5 billion people. That is the majority of people on earth.. Few will be chosen to survive and they will be intensely controlled. This is all about Technocracy, as Pat Wood and David Hughes have stated many times.
I get sinus infections and steady Eustachian tube inflammation, dyspnea, now for 4 years since the second shot. My doctor put me on Singular and cromolyn sodium but it doesn't help. He says well, we're addressing your mast cell dysfunction. But I doubt if deeper down, mast cell disruption is really the problem, but only the expression of systemic inflammation, and so addressing mast cells isn't the answer.
From the beginning, I maintained that, from what I understood about the mechanism for mRNA technology, the individual's genetic make-up would be altered if injected. I also said that each individual is unique; the injections will play quite differently for people; and scientists involved in this "research" had no idea how this technology would truly disrupt the human body. I'm very glad to see verifiable proof now arising.