THE CENSORED SCIENCE OF ADVERSE EVENTS: What Covid-19 Jabs Can Do to You

CONCLUSION: Covid-19 mRNA gene based injections introduce particles into the circulatory system. They will interact with the cells in the walls of the bloodstream at multiple places, causing the destruction of these cells, blood clots and/or a shortage of platelets. Understanding this makes it possible to explain many of the of the recorded adverse events.

Governments, health officials and pharmaceutical companies have insisted the mRNA injections are safe and refuse to consider the possibility that adverse events are actually caused by them. However the connection between many of the adverse events which follow Covid-19 jabs is not a mystery. Even before the roll-out of the "vaccines" had begun, some scientists and doctors have understood what could happen to people who got these injections. The purpose of this article is to investigate what happens after mRNA gene therapy is used as a protection from Covid-19 infection.
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I am not a medical doctor or a research scientist, however this article is based on the work of other people who are doctors and scientists. The location of their articles and discussions will be given in footnotes and their qualifications noted in an appendix. These scientists and doctors have been censored by mainstream media because they could allow us to understand that the Covid-19 jabs are actually dangerous. I consider what follows as well informed speculation, but would encourage others to do their own research to confirm or uncover mistakes in what is said here. I realise that other accounts of adverse effects of the mRNA jabs can be found, but I have chosen to rely on the work of three doctors who are members of the Doctors4CovidEthics.
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WHAT HAPPENS AFTER A JAB FROM PFIZER OR MODERNA?
The only way to understand the nanture of some adverse effects from mRNA vaccines like Pfizer and Moderna is to begin with an understanding of how these medications produce antibodies to protect people from a Covid-19 infection. This account is taken from the website of the Center for Disease Control, the CDC. It is the Offical Story.
"COVID-19 mRNA vaccines give instructions for our cells to make a HARMLESS piece of what is called the 'spike protein'. The spike protein is found on the surface of the virus that causes COVID-19.
"COVID-19 mRNA vaccines are given in the upper arm muscle. Once the instructions (mRNA) are inside the immune cells, the cells use them to make the protein piece (aka spike protein). After the protein piece is made, the cell breaks down the instructions and gets rid of them.
"Next, the cell displays the protein piece on its surface. Our immune systems recognise that the protein doesn’t belong there and begin building an immune response and making antibodies, like what happens in natural infection against COVID-19.
"At the end of the process, our bodies have learned how to protect against future infection. The benefit of mRNA vaccines, like all vaccines, is those vaccinated gain this protection without ever having to risk the serious consequences of getting sick with COVID-19."(1)
Lipid Nanoparticle
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The injection introduces millions of lipid nanoparticles which contain mRNA. This mRNA is an "instruction" to immune cells which makes them produce a spike protein on their surface if a particle is taken up by that cell. Then other cells in the immune system detect the spike protein as a danger and create antibodies in the same way it would if the person injected with the mNRA had instead come in contact with Covid-19 virus.

Explanation of Diagram: mNRA NPs in the diagram are the lipid nanoparticles (NP). Following the arrows in the diagram, the Carona mRNA (CAR = carona) goes from the nanoparticle to the cell where it makes a protein. This protein then becomes a Carona protein on the surface of the cell. In what follows, this process is understood as a cell's taking up the nanoparticle and its contents, the Messenger RiboNuclaic Acid and creating a spike protein on its surface. The spikes can be seen in the transmission electron micrograph of the Avian coronavirus.
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WHAT COULD POSSIBLY GO WRONG?
Dr Michael Yeadon believes the Official Account is mistaken in claiming the spike protein created on the surface of the immune cells is harmless. Instead he insists the spike protein is biologically active. In particular it is fusogenic, that is, it makes cells stick together and it can initiate blood coagulation, the formation of blood clots.(2) Further, the Doctors4CovidEthics insist the Official Account conveniently ignores the fact that after millions of these nanoparticles containing mRNA are injected into your arm, some of them will enter the bloodstream. Then some of the cells they encounter will take up the nanoparticles in the same way that the immune cells do.
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Endothelial cells lining veins and arteries.
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There are many different ways that the introduction of these genetic instructions can disrupt the complex biological systems which make up the human body. After reviewing the adverse events that have been recorded following the Covid-19 jabs, it would appear the damage caused to the circulatory system and the consequences of this damage has been an important area of concern. In what follows I will focus primarily on how blood clots play such a major role in these adverse events. At the end of the article I will discuss cell fusion, reactions at the injection site, and immune dependant enhancement.
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COVID-19 JABS CAUSE BLOOD CLOTS
Many of the side effects of the different Covid-19 jabs are caused by blood clots somewhere in the body. For example, a blood clot at the right spot in the brain will disable that part of the nervous system which controls movement. This can cause paralysis or involuntary movement of legs and arms. So how does this happen?
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Dr Wolfgang Wodarg, one of the Doctors4CovidEthics, explains that after the nanoparticles are injected into the muscle "it must be expected that at least in some cases the injected genetic information may leave the injection site by mistake or accidentally and more or less enter the bloodstream to be spread throughout the body."(3) Once the genetic information enters the bloodstream
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“..the nanoparticles containing the mRMA instructions will come into contact with the endothelial cells which line the walls of blood vessels. These cells will also interact with the nanoparticles by absorbing them and creating a spike protein on their surface, particularly in places with a slow blood flow. After the cells that make up the wall of the blood vessel take up the genetic information, the spike protein on their surface will be in contact with passing blood cells.
"It can be assumed, that such uptake in endothelial cells occurs particularly at sites with slow blood flow. This will presumably happen, where the contact time is long enough, such as during capillary passage or in the venous system following with low pressure and orthostatic narrow venous network."
"When such spike proteins, genetically engineered from our cells, enter the blood, they directly bind with the ACE2 receptors of platelets, which also leads to blood clotting and thrombosis. This has also been observed with whole coronaviruses entering the blood in rare cases. Thrombocytopenia so developed has also been reported in vaccinated individuals."
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The chain of events Dr Wodarg explains here can be summarised as follows: While some of the nanoparticles are taken up by the cells of the arm muscles and the immune cells, the rest of them enter the bloodstream. As they flow around the body they will be taken up by the endothelial cells lining the blood vessels, more perhaps in places with a slow blood flow. Then the endothelial cells will produce a spike protein and the contact between the spike protein and the platelets in the blood stream will create a blood clot.
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This can take place anywhere in the blood stream, and the specific location of the clot will determine the nature of the adverse events the person will experience.


HOW COVID-19 JABS CAUSE FURTHER DAMAGE TO THE LINING OF BLOOD VESSELS
This account of how Covid-19 jabs damage the epithelial cells of the blood stream comes from an interview with Dr. Sucharit Bhakdi by Taylor Hudak: "COVID Vaccine Blood Clot Risk Was Known, Ignored & Buried".(4) His comments explain in detail how two different processes take place which coincides closely with the account of Dr Wodarg. We should remember that both are members of the Doctors4CovidEthics who, after consulting with others, have written at least two letters to the medical authorities in the EU requesting that the roll-out of mRNA medication should cease because of the dangers discussed here. The following paragraph is my summary of Dr Bhakdi's points discussed in the ipodcast from 15:10 to 22:30.
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"The spike protein enables Covid-19 to enter cells. The mRNA vaccines put a billion genes (genetic instructions) for the spike protein into your arm. These stay in the arm, go into the lymph nodes or into the bloodstream. The ones in the bloodstream are taken up by the cells they come in contact with. Most of them are taken up by the cells of the blood lining, the epithelium. More are taken up where the blood flow is slow. Next the epithelial cells will cause the spike to appear on their surface as well as waste products. The spike protein is able to activate platelets it comes in contact with and that begins the process of forming blood clots. Further we have killer lymphocytes that recognise the waste of coronaviruses and it will try to kill the cell with the waste on the surface. By killing the epithelial cells that line the blood (stream) the killer lymphocytes damage the lining of the circulatory system and set off blood clotting. We have started seeing blood clots in the lungs and brain. Symptoms of blood clots in the brain (cerebral vein thrombosis): splitting headaches,  nausea, vomiting (as pressure in the brain goes up), losing consciousness, paralysis, deafness, blurred vision, can't speak properly, convulsions, jerking - loss of motor control. This is one of the major adverse events of these vaccines."
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In addition to producing blood clots caused by interaction between the spike proteins and platelets in the blood stream, when an epithelial cell produces a spike on its surface it also deposits the waste created by this process on its surface. Many healthy people have killer T cells in their bloodstream. These cells, also known as cytolytic T cells, or CD8+ T-cells, are T lymphocytes, a type of white blood cell that kills cancer cells, cells that are infected with viruses, or cells that are damaged in other ways.(5) The killer T cells are programmed to attack and destroy any cell which has such waste deposits on its surface. Since the epithelial layer is only one cell thick, if one or more are destroyed blood will leak out and this will trigger blood clotting.
Explanation of Diagram: Shows a killer T cell attacking an Epithelial cell infected with a virus. When lipid nanoparticles from the mRNA Covid-19 injections are taken up by endothelial cells and these cells deposit the waste created by this process, they will be attacked and destroyed by killer T cells in much the same way, by releasing perforin and cytoxin.
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It would appear that the Official Story presented by the CDC ignores several important phenomena. First, they seem to assume that ALL the nanoparticles will be taken up by the immune cells, even though there is no reason given why this should be so. Second they fail to recognize what Dr Yeadon explained above, the spike protein is biologically active. It can activate blood clotting in two different ways. Clots will form simiply by contact with platelets in the blood stream after the spike protein has been created by an epithelial cell. Or when epithelial cells take up the genetic instructions to produce a spike protein, they deposit waste materials on their surface. As soon as killer T cells detect this waste they will destroy these cells, create a hole in the blood vessel and this will initiate blood clots.
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CONSEQUENCES OF BLOOD CLOTS APPEARARING IN THE CIRCULATORY SYSTEM
These blood clots can occur almost anywhere, but the results differ widely, depending on the location. If they occur in the heart, they are called a pulmonary embolism. If they occur in the brain they cause what is known as cerebral venous thrombosis (CVT) or a stroke. Cerebral venous thrombosis is the presence of a blood clot in the dural venous sinuses (which drain blood from the brain), the cerebral veins, or both.(6) In their Rebuttal Letter to European Medicines Agency the Doctors for Covid Ethics note the following symptoms of CVST:
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Splitting headache/migraine blurred vision, nausea and vomiting.
Nausea
Vomiting
Dizziness
Loss of consciousness
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In severe cases people experience stroke-like symptoms including:
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Impairment of speech caused by an injury to the nerves which control the muscles that help produce speech.
Impairment of vision/blindness caused by an injury to the nerves which control the visual system.
Impairment of hearing caused by an injury to the nerves which control the the auditory system.
Body numbness
Weakness
Decreased alertness
Loss of motoric control, which could involve paralysis or involuntary movement of legs, arms.(7)
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This is Maddie. She is 12 and is now paralyzed from the
waist down, cannot urinate on her own and has extreme
neurological and gastrintestinal issues thanks to being
one of the guinea pigs in the Moderna trial. You can find
her story on Bitchute but I'll also share it in my Telegram
channel.
Ella Butler


.Paralysis
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Blood clot in the brain
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Blood clot in the heart
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I am in no position to say that an mRNA injection has caused these symptoms in people who experiences them after such an injection, but at the same time it is surely no accident that the analysis of the Doctors4CovidEthics predicts that such adverse events should be expected.
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MORE CONSEQUENCES OF BLOOD CLOTS
The Doctors4CovidEthics explain another condition caused by blood clots is disseminated intravascular coagulation (DIC), a condition in which blood clots form throughout the body, blocking small blood vessels. As we have seen, this can occur when epithelial cells with spike proteins on their surface contact platelets or when these cells have been attacked by T-killer cells. Symptoms may include chest pain, shortness of breath, leg pain, problems speaking, or problems moving parts of the body.(8)
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Disseminated Intravascular Coagulation

Disseminated Intravascular Coagulation
Adverse Event from Twitter
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If there are not enough platelets to form blood clots at all the points where the endothelial lining of the veins and arteries have been broken, then bleeding will occur. This may involve blood in urine, blood in stools, or bleeding into the skin. There are many reports of such bleeding into the skin, and it may also explain the excessive or unusual menstrual bleeding experience by women who have been given one of the mRNA injections.
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Thrombocytopenia is understood as an abnormally low level of platelets. What seems to happen to some people after getting a Covid-19 jab is that their entire supply of platelets and other means of creating clots has been used up, blood can escape freely into any area it can, either as lilttle spots or bigger blotches. As a medical novice I find it hard to distinguish some cases of Thrombocytopenia from disseminated intravascular coagulation.
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Thrombocytopenia

Thrombocytopenia

Adverse Events from Twitter


Explanation: This is one page of a document posted on Twitter which is alleged to be from the NHS in the UK. It warns of thrombocytopenia, cerebral venus thrombosis (CVT) as well as pulmonary embolism and hyperfibrinolysis. The fibrinolysis system is responsible for removing blood clots. Hyperfibrinolysis describes a situation with markedly enhanced fibrinolytic activity, resulting in increased, sometimes catastrophic bleeding. Fear of blood clots just a conspiracy theory?
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SPIKE PROTEIN CREATED BY COVID-19 JABS CAUSES CELL FUSION
In his discussion of mRNA injections Dr Wodarg also notes the ability of spike proteins to cause cell fusion.
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"In addition: the ability of the SARS-CoV-2 spike proteins to initiate cell fusions is very strong. The resulting giant cells can also lead to vasoobstruction, inflammatory responses, and microthrombosis."
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Dr Wodarg explains more about the harm from spike protein induced cell fusion in a discussion of a research paper published by the Paul Ehrlich Institute in Germany.(9) He is surprised that the warnings in the paper about spike proteins has been totally ignored even by the Institute itself:
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"This scientific paper, written with the participation of agencies director (the director of the Paul Ehrlich Institute itself), is quite something, because it was apparently published in order to once again point out the special dangers of corona infections. These consist in the fact that the spike proteins of the coronaviruses alone can also fuse neighbouring cells, which can eventually form a clump of up to a hundred fused cells and perish in the process.
"The work also found that the mere presence of the isolated spike proteins, without the viral body, can lead to such cell fusions on a large scale."
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The last sentence explains that the spike protein on its own, which is produced by every cell that takes up the mRNA instruction, is capable of causing cell fusion anywhere in the body.
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"In which organs this happens cannot be predicted. It must therefore be feared that the strong tendency to uncontrollable cell fusions triggered by spike proteins can cause severe tissue damage and corresponding immunological and haematological consequences. Tissue destruction, microthromboses and secondary immune complications could result in severe clinical pictures and death within a short time."
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An example of the kind of damage is the cell fusion in the lungs of patients affected with Covid-19, something not seen in other lung infections before.
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REACTIONS TO THE mRNA INJECTIONS AT THE INJECTION SITE
Another common side effect of the Covid-19 jabs is pain and a skin rash at the injection site. Dr Wolfgang Wodarg explains that when the nanoparticles containing mRNA are injected into the upper arm muscle
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"(...) there are not enough competent immune cells in the tissue of the m. deltoideus (deltoid muscle). And as soon as some closer cells in the muscle start to produce and present spike protein, there should be a strong and more and more generalising local immune reaction with swellings and pain."
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In other words the muscle cells in the arm respond to the nanoparticles by setting off an immune response of swelling and pain. How is this possible? It happens because when the muscle cell takes up the mRNA instructions from a nanoparticle and produce a spike protein on its surface, it also places the waste matter created by this process on its surface. Then the muscle cell will be  attacked and destroyed by the killer T cells which recognise that the muscle cell has been modified. This reaction is what produces the immune reaction experienced as pain and rash around the injection site.
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DR SUCHARIT BHAKDI DESCRIBES IMMUNE DEPENDENT ENHANCEMENT
Near the end of Taylor Hudak’s interview with Dr Bhadki she asks him: How dangerous are these these gene based vaccines? He says at 42 minutes: "They are so dangerous, in my opinion, that I get nightmares thinking that this vaccination is going to be installed on a permanent basis." At this point he begins to explain what I have paraphrased here. At the end of his discussion he explains "This constitutes immune dependant enhancement."
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"When mRNA nanoparticles are taken up by a cell, they produce a spike protein and and waste from the process on the cell wall. When not in action, killer T cells reside in lymphoid organs, lymph nodes and the spleen. They only come out into the bloodstream when they see the waste products on cell walls. They attack and kill our own cells which have waste products on their surface. This is kind of autoimmune reaction. When they are called to attack they carry out a clonal expansion. They divide and divide from 1 to 2 to 4 to 8 etc.
"After killing the unwanted cells and expanding their numbers the killer T cells go back to rest. So if the mRNA is injected a second time and is again taken up by cells, there are not 1 but 2, 4, 8 etc. killer T cells coming out in action. In this situation the immune system becomes overactive."
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The process Dr Bahkdi explains here is a well-known response of the immune system to an infection. It is explained in a web document produced by the University of Arizona as teaching material for biology:
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"An amazing feature of your immune system is that it remembers the infections it has fought. This makes it much easier to fight the same virus or bacteria a second, or third, or fourth time.
"Toward the end of each battle to stop an infection, some T-cells (killer T cells) and B-cells turn into Memory T-cells and Memory B-cells. As you would expect from their names, these cells remember the virus or bacteria they just fought. These cells live in the body for a long time, even after all the viruses from the first infection have been destroyed. They stay in the ready-mode to quickly recognise and attack any returning viruses or bacteria.
"Quickly making lots of antibodies can stop an infection in its tracks.  The first time your body fights a virus, it can take up to 15 days to make enough antibodies to get rid of it. With the help of Memory B-cells, the second time your body sees that virus, it can do the same in thing 5 days. It also makes 100 times more antibodies than it did the first time."(10)
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After the first mRNA vaccination the body will respond by developing killer T cells which are programmed to attack and destroy cells with the spike protein on their surface. Then, after the first infection is dealt with, these killer T cells replicate 100-fold, so there will be a much stronger immune reaction to the second vaccination than the first.
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Immune dependant enhancement has been recognized as a difficulty for creating a vaccine for the  SARS-CoV-2 virus, but the approval and use of these gene based vaccines has gone ahead nonetheless. Without much digging, I came up with the following two quotes from articles in the U.S. National Institutes of Health's National Library of Medicine (NIH/NLM). The first states openly that earlier studies have shown "anti-SARS-CoV-2 antibodies could exacerbate COVID-19 through antibody-dependent enhancement".(11) The second quote is rather more frightening:
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"At present, there are no known clinical findings, immunological assays or biomarkers that can differentiate any severe viral infection from immune-enhanced disease, whether by measuring antibodies, T cells or intrinsic host responses."(12)
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In other words, if someone comes down with a severe Covid-19 infection there seems to be no way to distinguish it from "immune enhanced disease" otherwise known as immune dependent enhancement. The only rather obvious clue would be that they have had a Covid-19 jab, but as we know the authorities will insist that there is no proven connection.
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[A point of clarification: In the medical literature I have seen immune dependant enhancement described as: cellular immune response,  viral interference, antibody dependent enhancement (ADE), pathogenic priming, vaccine associated disease enhancement (VADE), or autoimmune reactions overloading the immune system.]
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There is a video of a conversation between Dr Reiner Fuellmich, Professor Delores Cahill, and lawyer Viviane Fisher in which Prof Cahill explains the same dangerous reaction.(13) She states the immune dependent enhancement could even occur after the first mRNA injection because the person may have been infected by a coronavirus before. It is also explained in a famous article by James Lyons-Weiler: "Pathogenic priming likely contributes to serious and critical illness and mortality in COVID-19 via autoimmunity".(14) This important information has been known for years, but it has been completely suppressed or censored in order to hide the real dangers of the mRNA gene based vaccines.
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A FINAL WORD ON mRNA VACCINE INDUCED DAMAGE MECHANISMS
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My final word is simply that this article does not cover all the mRNA vaccine induced damage mechanisms. However there is a 34 page PDF by Dr.ssa Loretta Blogan you may wish to consult.(15) Her PDF contains over 100 references to relevant articles on the following subjects. I have reproduced some of her comments on each topic:
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ANTIBODY-DEPENDENT ENHANCEMENT (ADE)
The biological mechanism causing this particularly severe adverse reaction was observed during preclinical studies with SARS-Cov-1 vaccines. However, ADE has also been explored in depth in MERS, Dengue, Zika virus, Ebola, HIV and seasonal influenza.
The ADE mechanism is quite complex but can be summarized as follows: when a subject who possesses a sub-optimal antibody level (as a result of primary infection or vaccination) comes into contact with a similar virus and becomes infected, his immune system promotes infection and fatal complications of the disease. In other words, a proportion of the vaccinated are predisposed by the vaccination to developing serious and fatal complications of the very disease they are meant to be protected from.
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AUTOIMMUNE INFLAMMATORY SYNDROME
It would appear that the source of this adverse vaccine reaction, which has already been encountered among people vaccinated with “Pfizer” vaccine, and of serious complications reported in the literature following COVID-19, is a molecular mimicry mechanism, i.e. of sequence homology (similarity) between Spike proteins and human proteins from various tissues.
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VACCINE RESISTANCE
This phenomenon is related to the formation of mutant populations called quasispecies, typical of single-chain RNA viruses, also evident in SARS-Cov-2.
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NON-IGE MEDIATED PSEUDOALLERGY (CARPA)
Studies of RNAi release through cationic LNPs (nanoparticle liposomes) showed that polyamines such as polyethylenimine and poly-L-lysine led to high serum liver enzyme levels, reduced body weight, and dramatically reduced total leukocyte counts, suggesting a mechanism of immunosuppression after intravenous administration.
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SYSTEMIC REACTIONS
Recent human studies have demonstrated moderate and in some cases severe systemic or injection site reactions to several mRNA vaccine platforms. Potential safety issues that should be evaluated in future preclinical and clinical studies include local and systemic inflammation, biodistribution and persistence of the expressed immunogen, stimulation of autoreactive antibodies and potential toxic effects of any non-native nucleotides and components of the delivery system.
A possible concern could be that some mRNA-based vaccine platforms induce potent type I interferon responses associated not only with inflammation but also with autoimmunity.
By stimulating dendritic cell maturation and eliciting robust T- and B-cell responses, mRNA vaccines may activate autoreactive lymphocytes and reactivate autoimmune diseases. Therefore, individuals at increased risk for autoimmune reactions should be identified before mRNA vaccination and appropriate precautions should be taken.
Another potential safety issue could arise from the presence of extracellular RNA during vaccination. Naked extracellular RNA has been shown to increase the permeability of tightly packed endothelial cells and thus may contribute to edema.
Other studies have shown that extracellular RNA, acting as a DAMPS, also promotes pathological thrombus formation, and cardiomyocyte death. (Myocytes are muscle cells. Cardiomyocytes are the muscle cells of the heart.)
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NEUROLOGICAL DAMAGE ASSOCIATED WITH PRION PROTEIN FORMATION
Although there is long-standing evidence that human coronaviruses, such as SARS-CoV-2, can spread to the brain from the respiratory tract, the occurrence of gastrointestinal symptoms suggests that the gastrointestinal system is a possible route of invasion and transmission to the enteric nervous system (ENS).
While the effects of COVID-19 on olfactory and gustatory perception may be transient, the possibility of SARS-Cov-2 and other infectious agents may be the initial etiology of neurological and neurodegenerative diseases is well documented, 58 according to a mechanism called immuno-excitotoxicity.
Parkinson's disease (PD) is a common neurodegenerative disorder associated with the progressive loss of dopaminergic neurons located in the nucleus of the substantia nigra pars compacta (SNpc) of the midbrain due to the accumulation of α-synuclein (α-syn) aggregates. Interestingly, the prodromal or preclinical phase of PD is also characterized by olfactory and gastrointestinal symptoms.
It is important to note that the PD and Creutzfeldt-Jakob prion disease have been reported in the literature as diseases caused by COVID-19, and PD as a possible adverse reaction from mRNA vaccine.
Given the similarity between the mechanisms of COVID-19 damage and vaccine adverse reactions (see "Pfizer" paper), it is conceivable that many of the symptoms and pathologies associated with long-COVID may also be present as long-term consequences of vaccination.
[The "Pfizer" paper mentioned here is the UK publication "COVID-19 mRNA Pfizer- BioNTech vaccine analysis print" found at this location: https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/962405/COVID
-19_mRNA_Pfizer-_BioNTech_Vaccine_Analysis_Print.pdf]
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INTEGRATION IN THE DNA
It should be noted that while there is a theoretical concern for integration into the host genome with regard to plasmid DNA vaccines, there are four reasons this concern is not shared for mRNA-based vaccines.
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TWO AWKWARD QUESTIONS
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WHY ARE THEY DOING THIS TO US?
It is obvious that people are submitting to this gene based vaccination because of unprecedented media and political coverage of the Covid Emergency for over a year. But the other side of the question is: Why are the many politicians and public servants going along with it? Surely many of them realise that it is dangerous for the populations of their country? Is there something more at work than simple fear of being sacked?
Perhaps this is the answer: Are there more people in high places in the West who secretly believe there are too many people in the world? In other words, the doctrine preached by the small number of vocal eugenicists like Bill Gates and his father, or Boris Johnson and his father, is more widespread than we might have suspected. It could be there are many silent supporters why do not want to openly advocate this policy. They can let Gates and his friends do that. But they are more than happy to carry out this secret wish if they are allowed to under the Covid Emergency.
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ARE ALL COVID-19 JABS THE REAL DEAL?
When I started to investigate the biological consequences of the mRNA vaccines, it became quite obvious they can have a very powerful effect on our bodies. But if they are so powerful and dangerous, why aren't there more adverse effects and deaths? I can see several reasons:
1. People are biologically different, so, like other medications, different people will have different reactions based on their own biological makeup.
2. People of different ages also have better or worse immune systems. Perhaps the people who feel nothing - not even pain at the injection site - have non-functioning immune systems, so there will be no immune reaction to the muscle cells with spike proteins on their surface.
3. OR ARE PEOPLE GETTING A PFIZER JAB DO NOT ALL GET EXACTLY THE SAME SOLUTION PUT IN THEIR ARM? There is no way to know this, unless a whistlelblower comes forward or some of the vials happened to fall off the back of a truck and slip into a lab which could examine their contents. Will we ever know.....?
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FOOTNOTES:
3. Dangerous side effects of genetically induced production of SARS CoV-2 spike proteins
https://www.wodarg.com/english/
There is another interview with Dr Bhakdi: "Perspectives on the Pandemic | "Blood Clots and Beyond" | Episode 15" https://www.youtube.com/watch?v=pyPjAfNNA-U
9. Was a dangerous side effect of vaccination ignored by the Paul Ehrlich Institute? https://www.wodarg.com/english/
10. Memory Cells
11. A perspective on potential antibody-dependent enhancement of SARS-CoV-2
12. A perspective on potential antibody-dependent enhancement of SARS-CoV-2
13. LAWYER DR. REINER FUELLMICH, PROF. DOLORES CAHILL, LAWYER VIVIANE FISCHER QUESTIONING MRNA VACCINE
14. "Pathogenic priming likely contributes to serious and critical illness and mortality in COVID-19 via autoimmunity".(x) https://www.sciencedirect.com/science/article/pii/S2589909020300186.
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APPENDIX: MY THREE SOURCES:
Dr Sucharit Bhakdi is a Thai-German specialist in microbiology, having studied at the universities of Bonn, Giesen, Mainz, and Copenhagen. He also studied at the Max Planck Institute Of Immunobiology And Epigenetics in Freiburg, and is a professor emeritus of Johannes Gutenberg University Mainz, and from 1991 to 2012 was head of the Institute Of Medical Microbiology And Hygiene.
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Dr Wolfgang Wodarg is an internist, epidemiologist and pulmonary physician, specialist for hygiene and environmental medicine as well as for public health and social medicine. After his clinical activity as an internist, he was, among other things, a public health officer in Schleswig-Holstein, Germany for 13 years. He was a member for the SPD of the Bundestag from 1994 to 2009 and chair of the Parliamentary Assembly of the Council of Europe Health Committee.
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Dr Mike Yeadon is a former Chief Scientific Officer and Allergy and Respiratory Research Head with Pfizer Global R&D and co-Founder of Ziarco Pharma Ltd.
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and
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Dr.ssa Loretta Bolgan holds a graduate degree in pharmaceutical chemistry and technology, a PhD in pharmaceutical science from the University of Padua, and was a research fellow at Harvard medical school. From 2004 until the present, she has worked as a scientific consultant on investigations on quality issues, such as contaminants, of vaccine products, and the biological mechanisms which induce adverse reactions to vaccinations.

Russia's Diplomatic Response to President Biden's Sanctions - US Ambassador Advised to Leave Moscow

Copied from tweets by Veritas Semper Vincit @semper_vincit
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1. Ambassador John Sullivan was advised to leave Moscow
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2. Ten US diplomats will be expelled from Russia
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3. Moscow is introducing a ban on hiring staff from the Russian Federation and third countries for the US for the US embassy and other embassies
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(This is gonna be painful as Americans do not speak Russian or other languages; hey, they don't even speak English)
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4. ANY remaining US NGOs and foundations associated with the embassy and still operating will be  closed.
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(Sergei Lavrov: These organizations "directly interfering in Russia's domestic political life".)
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5. Americans coming to Russia for "short-term business trips, having diplomatic immunity when they are not US embassy's employees is over: limited to 9 / year, on a reciprocal basis.
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(This will deeply cut into CIA "business trips")
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6. The Russian Federation is unilaterally suspending the 1992 Memorandum of Understanding "on an Open Country": embassy staff has to inform inform the host country of a journey of more than 25 miles (40 kilometers) from the city of residence.
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(Sergei Lavrov says that the Americans often ignore this treaty, as usual. Americans will need granted permission from now on. Lavrov said that a US military attaché recently traveled to Central Russia without even mentioning this to Russian authorities.)
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After these retaliations done by the Russians, we can conclude that the US embassy - which is in fact Pentagon/ C!A headquarters in Moscow - and the NGOs - which are the civilian branches of Pentagon / C!A  and which were easily able to create color revolutions - have been dismantled by the Russians.
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About time.

ON THIS HALLOWED DAY - a compelling poem written to honour service veterans and ANZAC Day

Australian Voice has reprinted this poem with permission.
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ON THIS HALLOWED DAY
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Here we gather on this hallowed day
To pay our respects on ANZAC Day
Aussies and Kiwi’s we gather as one
And remember the fallen at the rising sun
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Of those who paid the ultimate price
With stories of bravery and sacrifice
Of wars fought long ago we still wonder why
So many brave people needed to die
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Today’s not about politics, anger, or debate
But reflection, two up and beers with your mates
To some we remind, it’s not a day off
It’s to commiserate and remember, your freedom had costs
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Our nation’s identity was born on a beach overseas
At a small piece of land, they called Gallipoli
And tragedy happened and some say we lost
But our lads did their job, no matter the cost
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Stories of those who lied and joined at fifteen
Chasing adventure and a boyhood dream
With no idea why, they wanted to settle the score
The enemies name irrelevant, there will always be more
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The little girl wears the medals her grandad earned
And watches the soldiers who’ve recently returned
Too young to understand or ever ask why
Waves her flag and cheers as they proudly march by
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The passage of time slowly welcomed the rest of the diggers
The great wars are no more but their memories linger
Korea, Vietnam and the ongoing Middle East
Will we ever find a way to just live in peace?
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So we say our prayers and look to the skies
But for the grace of god, it could be you or I
And Lest we Forget those who currently serve
We give our thanks and respect, it’s what they deserve.
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Stewart Elliott
20 April 2021
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Stewart Elliott lives on the Sunshine Coast in Queensland. While he holds the copyright he has made it freely available for publication provided he is given acknowledgment as the author.

NEW LIE FOR 2021: "Covid-19 Variants Escape Our Immune System So We Need Repeated Vaccination"

This is a reprint of an important message from Dr Michael Yeadon sent to Robin Monotti Graziadei.(1) The location of the article discussed by Dr Yeadon is given in the footnotes.(2)
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Robin Monotti Graziadei

Forwarded from Mike Yeadon

Dear Robin,
My message is a plea not to be fooled by the Great Lie of 2021, that “variants escape our immune defences so we’ll need repeated vaccination”.
I am deeply concerned about this lie & what it may portend.
Would you please share this as widely as you can?
Many thanks,
Mike
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Dear humanity,
I just read this ‘study’ claiming that, in vaccinated individuals, a variant of concern (VoC) appeared more frequently than in non-vaccinated individuals.
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They’re implying that such VoC ‘escape our immunity’, attacking us as if we had no immunity.
It’s complete nonsense.
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They tested ‘carriers’ (note choice of the word, which you’d never use, because the clear implication is of an ability to infect others with this VoC, something for which there’s absolutely no evidence) & these people are clinically well, with no symptoms.
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They did find the VoC more often than in a claimed matching group of unvaccinated individuals.
So what? There are numerous possible reasons for this, the most likely being that they’re not measuring what they think they are.
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Crucially, the VoC differs so little from the original virus that it’s impossible that, despite being immune after vaccination, it somehow “escapes their immune system”.
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The referenced work, showing that certain circulating antibodies are less effective in blocking the interaction involving a VoC (a synthesised portion of the virus & an artificial binding receptor for spike protein) is an example of very poor science.
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The whole set up plays to the idea that it is mostly or wholly just the antibodies that confer & are responsible for the functional immunity acquired after vaccination (or natural infection). Yet there’s no evidence for this at all.
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Indeed, it’s intrinsically unlikely. Antibodies are very large molecules which are mostly considered to be outside cells, either in blood or in the spaces between cells outside of the blood supply or, in some specialised circumstances, secreted onto outward-facing body surfaces (as described by Sucharit earlier in this thread).
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Plausibly, such antibodies could play an important role in preventing reinfection, during the period while the invading virus pathogen is in those compartments described, outside cells.
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But no serious immunologist would fail to recognise that, during clinically relevant illness caused by this virus, most of the battle between virus-infected tissues & our immune systems takes place when the virus is INSIDE OUR CELLS.
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The virus must be inside our cells in order to take over the replication apparatus of the cell, that being the only way in which the virus can multiply. Our cells are forced to make multiple copies of the virus, before that cell dies, liberating many more virus particles.
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During this process, repeated again & again, it’s not possible that antibodies, mostly restricted to the outside of cells, has any important function in host defence.
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That role is mostly performed by CD8+ cytotoxic T-lymphocytes (aka “T-cells” or “T-memory cells”). An infected cell has no choice but to signal that it’s occupied & it does so by placing on its external surface fragments of the invading virus.
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These signals are detected in a highly-specific way by T-memory cells, which then attack the infected cells & kill them, along with viruses inside.

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They do not attack healthy cells.
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Now, the breadth & detail of recognition of the virus and EVERY VARIANT of the virus is so great that it’s literally impossible for infected cells not to be detected as infected. This is because the changes to the virus are minuscule & so at most, only a few of the flags placed on the outside of infected cells are different from those our immune systems have seen before.

Conversely almost all the infection-signalling flags are identical to those we’ve seen before & our cellular immunity (T-cells) easily & speedily mop up infected tissues so readily that clinical infection is prevented.
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This isn’t a theory or speculation.

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DR YEADON HAS MORE TO SAY ABOUT COVID "VARIANTS:
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About 36 minutes into an interview with James Delingpole Dr Yeadon explains in more detail why Covid-19 variants are not any more dangerous that the oiginal Covid-19 virus.(3) This is my transcription - simplified somewhat - of the interview between 36:03 and 38:08.
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"You will probably all have heard...the story of virus variants. (...) The first time I heard this I thought oh that's interesting. (...) So I went to molecular biology and went to have a look and there was one amino acid change. I thought, that's quite unlikely to alter its behaviour. Let me explain why. This (the Covid-19 virus) is the largest, or one of the largest, virus ever sequenced. It contains 10,000 amino acids. Those are the building blocks of a protein. What that means is that if you changed 100 of them that would be a 1% change. But I've looked and the most different variant, the one that's furthest away from the virus first sequenced in Wuhan, China is 27 amino acids, less than .3% different. In other words it is 99.7% identical to the original. I assure you that the human immune system is much cleverer than that. It's impossible for a variant that differs by .3% that that will evade immunity. So the stuff you hear about, advisors saying we're not quite sure if the vaccine will work as well against this one or against that one...  It's bullshit."


FOOTNOTES:

1. https://t.me/robinmg/2287

2. Evidence for increased breakthrough rates of SARS-CoV-2 variants of concern in BNT162b2 mRNA vaccinated individuals https://www.medrxiv.org/content/10.1101/2021.04.06.21254882v2

3. The interview can be found here: https://delingpole.podbean.com/e/dr-mike-yeadon-1617215402/

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HOW WE CAN GET OUT OF THE FINANCIAL CRISIS THE WORLD ECONOMIC FORUM HAS PLANNED FOR US

INTRODUCTION
This is intended to follow on from “Is This the Endgame Part 1”.(1) In that article I explained why the World Economic Forum will almost certainly engineer a cyber attack on the Global financial system sometime after July this year. I also argue that it will consist in an attack on the weakest link among the major banks in the world. This will damage that bank’s “ability to meet its payment or settlement obligations, which could trigger a contagion effect where other financial institutions would not be able to meet their settlement obligations.”(2)
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Here is my prediction of how the financial community and governments will respond to a situation in which “financial institutions would not be able to meet their settlement obligations.”
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“We did a bail-out of the banks before but it didn’t work and it cost too much. This time we need to do something different, like replace cash with digital Central Bank money. And while we are at it, if you want some of this money, we need to identify who you are and make sure you are healthy. We just happen to have a digital ID system handy. This is also just what we were thinking about so you can prove you have had the latest Covid-19 vaccination. It can be all put together in one handy package: a universal ID system to guarantee you have access to money and and access to most venues.”
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Is this an offer we can’t refuse?
.
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THERE IS A WAY THROUGH THIS, BUT IT’S NOT EASY
We can’t get out of the current political situation just by saying “I won’t wear a mask” or “I won’t get the jab”. To really understand what is going on under the cover of the Covid-19 pandemic we must start with the realisation that the current financial system is finished. It is on life support. The super-rich know it cannot last forever. You will never see this in the media because the most important element in the financial system is confidence or trust. No bank is going to tell you it is bankrupt until the day after it shuts its doors.
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Why are they worried? They know what happened after the 1929 crash. There were powerful social movements for changing the system, and they know that this would arise all over again with many saying “I told you so.” The goal of the Great Reset is to begin a new financial system without the debt that has accumulated in the system we are using now. Digital currency is new, but the central part of the “new” system will be the same: banks will still loan money and collect the interest on these loans. Banks are privately owned corporations who must maximise profit and their main source of income is the payment of interest. This will not change in the Great Reset. The total surveillance and control is to make sure nobody can challenge their system.
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So the real political problem is not just getting rid of the draconian rules and mindless vaccinations. In the event of a financial disaster of the kind I have described, each country must continue to use its own financial system. They cannot rely on private banks’ loans with their interest payment, or else we will recreate the same system which has developed the monster called the Great Reset.
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When the financial system crashes, the only way to escape being trapped into their new digital money is for countries to instantly begin issuing their own currency again both digitally and in cash. We live in a money economy and we must have money to survive. If we don’t want the digital money of the Reset, each country must continue with their own currency to make sure food supplies are available and people have the money to buy them. There will be many details to work out, like compensation for depositors and investors, but the first priority must be for food. The more unrest there is, the more attractive the bank’s new money will be.
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But remember: If the financial system crashes, everyone will lose savings, deposits and investments. People should have no reason to love or trust the same banks that stole their money, and new political leaders must arise quickly to provide a viable alternative. The time to start that process is now!
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WE CANNOT ESCAPE THE COVID EMERGENCY WITHOUT POLITICAL LEADERS AND A CLEAR POLITICAL PLAN
If there are no leaders and no plan when people lose their savings, deposits and investments, the panic, confusion and chaos will almost guarantee that people will choose the digital ID, vaccination and the central bank digital money. The alternative is simply starvation, and this is what the masters of the Great Reset will rely on.
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While all this is difficult enough, there is one more gigantic obstacle to face: orthodox neo-liberal economic thinking, known as the Washington Consensus. It became public with Margaret Thatcher’s There Is No Alternative (TINA) and it is now the only “respectable” economic theory. One way to understand neo-liberal theory is this: Neo-liberals assume that the government’s budget is like the household budget. To run a household you need to have a surplus, more income than expenditure so you can avoid bankruptcy. In a government, the income is taxes and to achieve a surplus you need to practice austerity, spending as little as possible. In case the expenditure is greater than the income from taxes, the government’s budget is in deficit and it must borrow money to make up the difference.
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Since this is how all economists, government advisers and bankers think, how will they respond to the kind of financial collapse I have described? Our economies thanks to Covid-19 restrictions are dead and tax revenue is down. Governments are already in deficit, so will they want to spend more just to help ordinary people?
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They may be prepared to spend, but it will be the Universal Basic Income or UBI. They will use “austerity” as a reason for not compensating people for the money lost when the banks became bankrupt.
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So what is the alternative? I am not qualified to argue in detail against the neo-liberal approach, but 20 years of very destructive austerity policies should have taught us that we must find some other alternative. For more than 100 years economic theory has been a much disputed topic, and only recently has a kind of absolute neo-liberal orthodoxy been enforced on us, not unlike the orthodoxy of Global Warming or the recent orthodoxy about the treatment of viral infections. There are alternative economic theories out there and we now have a very urgent reason for finding a better alternative than the banker-friendly neo-liberal mind-set.
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I would like to finish with what seems a simple point of common sense. Thanks to “austerity” we have been told again and again there is not enough money for housing, education, health, public transport, etc. However when a government is at war, nobody ever says: “We can’t fight that war. We don’t have enough money.” There is always enough money for war. So I will remind you that the Great Reset, the Covid-19 pandemic and a financial disaster caused by a mysterious cyber attack are all a part of a continuous war on us, the ordinary people of the world. We are being attacked using a new kind of hybrid warfare funded out of the reserves of the world’s super-rich. The method of attack is to take over our political leaders and instituititons and force them to do their bidding. The only answer to this is to replace our leaders with people who are sworn to protect us and our country, and who respect the laws we have developed over many years.
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Our only protection from the Globalists and their World Government is our own nation-state. This is why every effort is made by the Globalist Resetters to undermine nation-states by divide and rule tactics like: masks vs no masks, vaccines vs no vaccines, women vs men, black vs white. They also have worked for years to introduce hundreds of thousands of people into Western Europe, the UK, the USA who are often given better treatment and those who have lived there for generations. Each country must have full control of their own borders, and it is interesting that Globalists do not insist than Japan or China admit “refugees” in the same way they are forced on the West. They even try to undermine history and tradition by attacking statues or forbidding the annual commemoration of the country’s war dead.
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An independent or sovereign nation-state has control of its money, a military, police and courts to enforce the laws it is entitled to make. Globalists want to destroy all of this so that giant corporations face no organised opposition to whatever they want to do to increase their profits. Some like to believe that nation-states are inherently evil in themselves. I will not argue against this here, only remind you we have already seen the Globalist New World Order in action. No recognition of any established law, right or convention. Only government directives = inhuman orders which have done much harm to people, and they have only gotten started. If you don’t want to be caught in their grip forever, you must fight against them now!
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FOOTNOTES:
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IS THIS THE ENDGAME: Use Financial Collapse to Force Vaccination, Digital ID and Cashless Society?

INTRODUCTION
I have just found an article which allows us to understand how the goal of the world’s super-rich – the Great Reset – can become a reality in the near future. It is an in-depth discussion of an upcoming Financial Cyberattack simulation Cyber Polygon 2021.(1) It provides an answer to this important question: We know what the super-rich want to achieve, but how are they going to do it?
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CYBER POLYGON 2021 SHOWS THE NEXT PHASE OF THE GREAT RESET
Those of us who are seen as conspiracy theorists know what has happenen in the last year was part of a well-planned exercise to change how the world is run. It is a plan developed by the world’s super-rich and implemented through institiutions and government agencies they control as well as countless NDOs. It has been most recently been publicly described as the Great Reset. In 2019 World Economic Forum, the public face of the Great Reset, held Event 201 in which the Covid-19 “plandemic” was discussed in a war-game exercise. As we all know, it came to pass early in 2020. The Emergency the “plandemic” justified has led to the complete takeover of virtually all governments by more or less invisible advisors who dictate the same draconian policies everywhere under the guise of a health emergency.
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Participants in the Cyber Polygon 2020
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In 2020 the World Economic Forum ran a high-profile cyberattack simulation that targeted the financial industry called Cyber Polygon. Now they have plan for a similar event this year, called Cyber Polygon 2021:
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“On Wednesday, the World Economic Forum (WEF), along with Russia’s Sberbank and its cybersecurity subsidiary BI.ZONEannounced that a new global cyberattack simulation would take place this coming July to instruct participants in “developing secure ecosystems” by simulating a supply-chain cyberattack similar to the recent SolarWinds hack that would “assess the cyber resilience” of the exercise’s participants.”(2)
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This exercise is notible for the prominent inclusion of Russia via its Sberbank and its cybersecurity subsidiary BI.ZONE.
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“Together with the World Economic Forum, BI.ZONE, a subsidiary of Sberbank, manages the Cyber Polygon project. Sberbank’s largest shareholder, as of last year, is the Russian government, and it is thus often described by English-language media outlets as a state-controlled bank. Other participants include IBM, Interpol, Ericsson, Mobile TeleSystems, the Cyber Peace Instutiute, funded byMicrosoft, Facebook, Mastercard, and the Hewlett Foundation.”(3)
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On the basis of what we have seen already, there is little doubt that a successful cyber attack on the world’s financial system will take place some time after Cyber Polygon 2021, perhaps near the beginning of 2022, if they follow the same schedule.
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CAN WE PREDICT  WHAT WOULD HAPPEN TO ORDINARY PEOPLE IN A FINANCIAL CYBER ATTACK?
In 2016 the World Economic Forum published a paper “Understanding Systemic Cyber Risk”.(4) This outlined how cyberattacks could result in the following problems for the financial system as a whole. I will explain each of them briefly here and show what the most likely outcome of such an attack would be.
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1. Failure of an institution’s ability to meet its payment or settlement obligations, which could trigger a contagion effect where other financial institutions would not be able to meet their settlement obligations.
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One of the hidden activities of banks is that each day they must settle what they owe each other. If you make a payment of $10 to Coles using an ANZ card, but Coles banks with the Commonwealth Bank, then the ANZ must pay your $10 to the Commonwealth so they can deposit it in Coles’ account. These are the daily “payment or settlement obligations” which keep the economy alive. Millions of these invisible transactions are carried out to enable most but not all of our daily activities.
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If one large bank cannot pay what it owes to other banks, they in turn may no be able to pay other banks or large corporations what they must pay them because of other legal obligations. This could lead to a cascade of bank failures in which they can no longer meet their obligations like giving you the money you have in your bank account. “Sorry but we don’t have enough money to pay you.” Banks are after all private corporations which have the overriding goal of making a profit. This would mean that your money would just disappear, and to the best of my knowledge banks do not guarantee to replace your money if it were to disappear in this way. In the 19th and early 20th century banks often failed in this way. This produced a real hatred of banks until modern legislation and decades of a public relations campaign has made them appear to be responsible actors in the economy.
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2. Failure or severe or prolonged disruption of a core payment and settlement system, which can be compromised at various endpoints, affecting multiple country and locations’ securities markets.
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This is a different kind of problem. Again there are more or less invisible (to us) payment systems to transfer money from major corporations or single individuals to corporations, banks or individual all over the world. Some of these transactions are involved in buying or selling the financial securities we see listed on stock exchanges. Trading these securities is a central part of doing business for major corporations, so a disruption to buying and selling securities on the stock market or other trading locations would jepordize the trillions of dollars of assets locked up in the paper economy of high finance.
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3. The loss or compromise of the availability and integrity of key financial data.
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Although most people don’t realize it, virtually all of our money exists as files in private banks. These files show what are your assets and liabilities (loans) and the assets (your loans) and the liabilities of the banks. But banks and other financial insitutions also keep track of the ownership of stocks, bonds and other financial instruments. It is the “loss or compromise” of this “key financial data” that would damage or destroy the financial system itself. In plain English, this key financial data shows who owns what assets. If this data was even compromised, that is changed, investors would panic because they might not be able to prove they owned what they thought they owned.
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4. Widespread loss of trust and confidence in the payment and settlement systems.
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Widespread loss of trust and confidence like this would show up as people refusing to deal with banks or credit cards, preferring instead to deal only in cash. Remember than 100 years ago people only had cash and banks only had paper records of their financial dealings. If there was no confidence in the world global financial system our world would not come to an end, but it would be different for a while until a better system could be organized in each country. The global financial system is good only for global corporations and globalist plans. The Pyramids, the Cathedrals in Europe, and the Empire State Building were all constructed without the contemporary global financial system, the World Bank, the IMF, or even WEF.
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Now we have seen what might happen to the world financial system in a future cyber attack, I will predict that it is only the first altermative that we should expect in any real attack. Why? Because this kind of attack limits damage to the commercial, retail banks that deal with everyday financial transactions. The other three possibilities would damage the wealth of the super-rich and other major investors. They don’t want to see damage to trade on stock markets, alteration or destruction of records of ownership, or a total collapse of the world financial system. So if the WEF and friends organize a cyber attack, I expect that they will search out the weakest link among the major banks in the world. They, and the cyber criminals, will get the blame for our savings disappearing as if someone had simply hit the DELETE key.
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We might even find a clue in the report of the Cyber Polygon exercise in 2020. The investigators found:
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“21% of the teams (taking part in the 2020 exercise) could not earn a single point for the second round of the second scenario (threat hunting). This was attributed to ‘Threat Hunting’ being a relatively novel approach and the majority of organisations lacking experience of applying its techniques in practice”.(5)
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If you wanted to launch a cyber attack, wouldn’t this be useful information? Perhaps we should see Cyber Polygon exercises as fishing expetitions to find the best way to mount a cyber attack. Is this like letting a gang of thieves install your security system?
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SO WHAT WOULD HAPPEN NEXT?
In the WEF document which outlines the potential risks of a cyber attack on the global financial system they provide this answer:
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“In such a scenario, central banks may be forced to take exceptional measures, such as the injection of liquidity funds, repurchase agreements, guarantees to extend the settlement window, and reductions in the cost of intraday and overnight borrowing, among others.”(6)
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But would they do that if they really wanted to destroy the assets of ordinary people and small business? If we look at the 2008-9 crisis, we find that such measures were in fact used, but only to protect the big end of town, the major creditors and corporations. This “bail-out” using money from the Federal Reserve system did nothing to help ordinary people through the crisis. Instead I can hear them say something like this:
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“We did a bail-out of the banks before but it didn’t work and it cost too much. This time we need to do something different, like replace cash with digital Central Bank money. And while we are at it, if you want some of this money, we need to identify who you are and make sure you are healthy. We just happen to have a digital ID system handy. This is also just what we were thinking about so you can prove you have had the latest Covid-19 vaccination. It can be all put together in one handy package: a universal ID system to guarantee you have access to money and and access to most venues.”
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Is this an offer we can't refuse?
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In my next article I show how we can escape the WEF plan for our slavery.
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HOW WE CAN GET OUT OF THE FINANCIAL CRISIS THE WORLD ECONOMIC FORUM HAS PLANNED FOR US
APPENDIX: WHO COULD POSSIBLY WANT TO SEE THE COLLAPSE OF THE FINANCIAL SYSTEM?
It may come as a surprise that an editor of the “Financial Times” thinks that a financial collapse would be a jolly good idea. In an article “Time for a great reset of the financial system” Chris Watling argues that the system set up after the US abandoned the Gold Standard that was established near the end of WWII in the Bretton Woods agreement should not continue.(7) He says this system is “tired” and has “reached the end of its usefulness”. While he cites “rising inequality” and the high cost of houses, the real problem is $25 trillion of government debt. What would a reset of the financial system look like? “As part of that there should be widespread debt cancellation, especially the government debt held by central banks.” What about the rest of us? “Whether debt cancellation extends beyond that should be central to the negotiations between policymakers as to the construct of the new system.”
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“The key reason that many western economies are now overly reliant on consumption, debt and house prices is because of the set-up of the domestic and international monetary and financial architecture. A Great Reset offers therefore opportunity to restore (some semblance of) economic fairness in western, and other, economies.”(8)
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What Chris Watling fails to explain is that after Lehman Brothers investment bank collapsed, none of the policies which led to the financial crash of 2008 have changed. There was no thought of fundamental reform then.
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“We are all familiar with the course of action taken from 2008-9: colossal bank bailouts enacted (without public consultation) that favoured creditors, not debtors, despite using taxpayer money. Quantitative easing (QE) has pumped trillions of dollars into the global financial system, unleashing a fresh wave of speculative investment and further widening income and wealth gaps.”(9)
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We must not forget that the vast amount of consumer credit we all take for granted actually has a short history. In 1958 the Bank of America launched its first BankAmericard which was renamed Visa in 1976.(10) In the beginning they were handed out like confetti by banks. They were sent to you whether you wanted one or not. The banks might want to change things now, but they have organised and managed the financial system for decades, so the problems they see are problems of their own making.
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Why is a reset of the financial system important now? Because the problems which were revealed in the 2008-9 crash have gotten much worse.
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“Banks may be relatively safer and possess a bigger crisis toolkit, but the risk has moved to the largely unregulated shadow banking system which has massively increased in size, growing from $28 trillion in 2010 to $45 trillion in 2018. Even major banks like JP Morgan are forewarning an imminent crisis, which may be caused by a digital ‘flash crash’ in which high frequency investments (measuring trades in millionths of a second) lead to a sudden downfall of global stock markets.”(11)
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The problem is that the debts in the system are so large than governments can no longer bail the system out as they did in 2008-9. So the super-rich have decided that rather than wait for another crash which would obviously be blamed on them, they will organise a cyber attack on the system to take the blame. Much as “Covid-19” is used to justify our loss of freedom and the bankruptcy of small business, they will blame “hackers” for the collapse of a system which has always been a house of cards.
.
.
FOOTNOTES:
2. Ibid.
3. Ibid.
5. Ibid.
6. Ibid.
8. Ibid.
11. Op cit.

Why Will Many More People Die From mRNA Vaccines?

INTRODUCTION
I have posted three articles in recent weeks about the immediate side effects of mRNA vaccines:
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Dr Tenpenny Explains A Serious & Potentially Deadly Side Effect Of mRMA Vaccines (1)
Some Side Effects Are Not A Coincidence: mRNA COVID-19 Vaccines Cause Lymphadenopathy (2)
mRNA Vaccines Create An Autoimmune Response Causing Thrombocytopenia, Bleeding And Blood Clots (3)
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In this article I will explore the more long term consequences of these medications.
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HOW WE KNOW MRNA VACCINES ARE NOT SAFE?
We have been told over and over that mRNA vaccines are safe. It may be hard to believe, but there is ample evidence that they are not safe at all. This issue is discussed by Prof Delores Cahill in the video interview below. While I have investigated some of the immediate consequences of mRNA vaccination, Prof Cahill concentrates on is the long-term consequences of these injections. You should realize that Prof. Cahill was recently dismissed from her academic post at University College Dublin, and this video cannot be posted on Twitter at its original location on ButChute.(4)
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Lawyer Dr. Reiner Fuellmich, Prof. Delores Cahill, Lawyer Viviane Fischer Questioning mRNA Vaccine
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How can we know what the long-term consequences of the mRNA vaccines are if they are new, and have never been used on humans before? We can know because over a decade ago they were tested on a range of animals in an effort to develop a vaccine for SARS. This video is one of many discussions of the consequences of injecting animals – mice and ferrets – with gene derived “vaccines” like those being used today.
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In the animal studies, the animals were first vaccinated against SARS. Then at a later time they were presented with a real world SARS virus. This initiated a clotting immunopathology in the lungs and they all died. Prof Cahill explains that the same thing can happen with SARS or Covid-19 in a different order. If you have already come into contact with Covid-19, your immune system will already be primed to attack it if it appears again. If you are then vaccinated with the mNRA vaccine, the spike protein from the Covid-19 virus will be generated in many places in your body by the immune system. (This is how the vaccine works.) These presentations will then be attacked by your primed immune system, so your immune system will be attacking itself. This is what an antoimmune disease consists of, and it will produce the same clotting immunopathology in the lungs.
If you want to have a deeper understanding of the biology involved in this I need to reproduce part of an earlier article which explains how mRNA vaccines work and how this sets up an autoimmune response in humans and other animals.
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HOW AN mRNA VACCINE WORKS
We must begin with a description of how an mRNA vaccine works. This account is taken from a website of the Center for Disease Control, the CDC.
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"COVID-19 mRNA vaccines give instructions for our cells to make a harmless piece of what is called the “spike protein.” The spike protein is found on the surface of the virus that causes COVID-19.
COVID-19 mRNA vaccines are given in the upper arm muscle. Once the instructions (mRNA) are inside the immune cells, the cells use them to make the protein piece. After the protein piece is made, the cell breaks down the instructions and gets rid of them.
"Next, the cell displays the protein piece on its surface. Our immune systems recognize that the protein doesn’t belong there and begin building an immune response and making antibodies, like what happens in natural infection against COVID-19.
"At the end of the process, our bodies have learned how to protect against future infection. The benefit of mRNA vaccines, like all vaccines, is those vaccinated gain this protection without ever having to risk the serious consequences of getting sick with COVID-19."(5)
IMAGE FROM WIKIPEDIA(6)
The “immune cells” in the description above are known as Dendritic cells. "Their main function is to process antigen material and present it on the cell surface to the T cells of the immune system."(7) Other cells in the body "can potentially absorb vaccine mRNA, manufacture spikes, and display spikes on their surfaces, however dendritic cells absorb the mRNA globules much more avidly."(8)
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"Once the viral antigens are produced by the host cell, the normal adaptive immune system processes are followed. Antigens are broken down by proteasomes, then class I and class II MHC molecules attach to the antigen and transport it to the cellular membrane, 'activating' the dendritic cell. Once the dendritic cells are activated, they migrate to lymph nodes, where the antigen is presented to T cells and B cells.This eventually leads to the production of antibodies that are specifically targeted to the antigen, resulting in immunity."(9)
.
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HOW mRNA VACCINES CAUSES AN AUTOIMMUNE RESPONSE
This is the first comment on mRNA vaccines in a letter the doctyors4covidethics sent to the European Medicines Agency.(10)
“1. Following intramuscular injection, it must be expected that the gene-based vaccines will reach the bloodstream and disseminate throughout the body [1].”
.
This is the third comment:
.
“3. It must be expected that during expression of the vaccines’ nucleic acids, peptides derived from the spike protein will be presented via the MHC I — pathway at the luminal surface of the cells. Many healthy individuals have CD8-lymphocytes that recognize such peptides, which may be due to prior COVID infection, but also to cross-reactions with other types of Coronavirus.[3; 4] [5]. We must assume that these lymphocytes will mount an attack on the respective cells.”
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In the account given by the CDC, the nanoparticles in the vaccine will enter and be processed by the dendritic cells. Then the “cell displays the protein piece [it has created from the nanoparticle] on its surface. Our immune systems recognize that the protein doesn’t belong there and begins building an immune response and making antibodies...” A passage from Wikipedia explains this process as follows: “Once the dendritic cells are activated, they migrate to lymph nodes, where the antigen is presented to T cells and B cells.”(11)
.
But the doctors4covidethics explain that many people will have been exposed to COVID or other types of Coronavirus. This means that the “spike” protein (made up of long chains of amino acids) which occurs on all coronavirus or peptides (smaller chains of amino acids) which are parts of the spike protein, will be recognized as belonging to a pathogen. Thus when the dendritic cell displays “the protein piece” created from the vaccine’s nanoparticle the immune system will not “begin to build an immune response and make antibodies...” or just “migrate to the lymph nodes”. Instead, since the dendritic cell displays a protein piece created from the vaccine nanoparticle, it will be attacked by the CD8-lymphocytes that recognize such peptides as pathogens.
.
We can see that in the story the CDC tells assumes nobody has been exposed to COVID or any other types of Coronavirus. They assume the immune system is ignorant of the threat of COVID, and the mRNA vaccine is going to teach the immune system to be prepared to attack it. But introducing the spike protein will not "teach" the immune system anything if a person has had some previous exposure to any type of Coronavirus. The cell which displays the recreated spike protein will be attacked because it has already been recognized as a pathogen and the immune system via the CD8-lymphocytes will destroy it. So what’s going on in the lymph nodes? There is a hyperimmune reaction to chronic antigenic stimuation, autoimmune activity, and the secretion of large amounts of antibodies.
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PRIOR KNOWLEDGE OF THE DANGER OF MRNA VACCINES
In this section I will present just a few comments which highlight the dangers of mRNA vaccines based on the earlier experimentation. This is a report of what happened in the original experiments ca. 2009:
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“In SARS, a type of ‘priming’ of the immune system was observed during animal studies of SARS spike protein-based vaccines leading to increased morbidity and mortality in vaccinated animals who were subsequently exposed to wild SARS virus. The problem, highlighted in two studies, became obvious following post-vaccination challenge with the SARS virus found that recombinant SARS spike-protein-based vaccines not only failed to provide protection from SARS-CoV infection, but also that the mice experienced increased immunopathology with eosinophilic infiltrates in their lungs. Similarly, found that ferrets previously vaccinated against SARS-CoV also developed a strong inflammatory response in liver tissue (hepatitis). Both studies suspected a ‘cellular immune response’.”(12)
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This cellular immune response has several descriptions in the scientific literature: viral interference, Antibody Dependent Enhancement (ADE), Pathogenic priming, vaccine associated disease enhancement (VADE), or autoimmune reactions overloading the immune system. This is how one biologist explains it:
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“The ADE (Antibody Dependent Enhascement) mechanism is quite complex but can be summarized as follows: when a subject who possesses a sub-optimal antibody level (as a result of primary infection or vaccination) comes into contact with a similar virus and becomes infected, his immune system promotes infection and fatal complications of the disease. In other words, a proportion of the vaccinated are predisposed by the vaccination to developing serious and fatal complications of the very disease they are meant to be protected from.”(13)
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Now consider this passage from Wikipedia:
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“ADE [or cellular immune response] may cause enhanced respiratory disease and acute lung injury after respiratory virus infection with symptoms of monocytic infiltration and an excess of eosinophils in respiratory tract. ADE along with type 2 T helper cell-dependent mechanisms may contribute to a development of the vaccine associated disease enhancement (VADE), which is not limited to respiratory disease. Some vaccine candidates that targeted coronaviruses, RSV virus and Dengue virus elicited VADE, and were terminated from further development or became approved for use only for patients who have had those viruses before.”(14)
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While this passage makes it quite clear that vaccines aimed at coronaviruses (namely the mRNA Covid-19 vaccines) “may cause enhanced respiratory disease and acute lung injury after respiratory virus infection”, at the end of the article under the heading “Misinformation related to the COVID-19 pandemic” we find this:
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“ADE has been observed in animal studies during the development of coronavirus vaccines, but as of 14 December 2020 there had been no observed incidences in human vaccine trials. Anti-vaccination activists cite ADE as a reason to avoid vaccination against COVID-19, but the expectation is that ADE would have already been observed in human trials if it were a risk. "Overall, while ADE is a theoretical possibility with a COVID-19 vaccine, clinical trials in people so far have not shown that participants who received the vaccine have a higher rate of severe illness compared to participants who did not receive the vaccine.”(15)
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Note the date: 14 December 2020. There had been few if any vaccinated humans at that point. As I explained above, evidence of such reactions has been found, but you won’t find it in Wikipedia.
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WHAT WENT WRONG?
Why did companies and regulators  develop and release mRNA vaccines given this well-known problem? Some people warned of the dangers as follows:
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“Challenge of mice given any of the vaccines led to occurrence of Th2-type immunopathology suggesting hypersensitivity to SARS-CoV components was induced. Caution in proceeding to application of a SARS-CoV vaccine in humans is indicated.”(16)
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You may have your own answer to this qustion, but mine is simply that they did not want a “safe” vaccine. They wanted one that would kill people and thereby “solve” the “overpopulation” problem. I think this is shown by the fact that they are covering up the immediate consequences of vaccination, they refuse to allow autopsies, and while they talk about “safety” they are not really interested in the deaths and injuries which have resulted.
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Careful observers are aware that Covid-19 is not a health problem. Covid-19 is a viral infection that governments have used to justify removing all basic freedoms on the grounds of a medical “emergency”. Covid-19 is not about health but control, and it may also be about killing off part of the world’s population with medications that are supposed to “Save Lives”.
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FOOTNOTES
10. "Urgent Open Letter from Doctors and Scientists to the European Medicines Agency regarding COVID-19 Vaccine Safety Concerns”; https://doctors4covidethics.medium.com/urgent-open-letter-from-doctors-and-scientists-to-the-european-medicines-agency-regarding-covid-19-f6e17c311595
12. James Lyons-Weiler, "Pathogenic priming likely contributes to serious and critical illness and mortality in COVID-19 via autoimmunity"; https://www.sciencedirect.com/science/article/pii/S2589909020300186
13. Dr.SSA Loretta Blogan, "mRNA VACCINE INDUCED DAMAGE MECHANISMS", Pdf here: https://drive.google.com/file/d/1Vol-S4Ac5Ws83zv1FYa5FGfgOCUH402_/view
15. Ibid.
16. Chien-Te Tseng and others, "Immunization with SARS coronavirus vaccines leads to pulmonary immunopathology on challenge with the SARS virus", https://pubmed.ncbi.nlm.nih.gov/22536382/
If you want to look at more scientitific literature on this subject download the Pdf by Dr.SSA Loretta Blogan, “mRNA VACCINE INDUCED DAMAGE MECHANISMS”.

mRNA Vaccines Create An Autoimmune Response Causing Thrombocytopenia, Bleeding And Blood Clots

INTRODUCTION
Early in January 2021 a Florida doctor, Dr. Gregory Michael, died of Idiopathic Thrombocytopenic Purpura, a rare autoimmune disorder that causes low platelet levels. Many of us believe the Thrombocytopenic Purpura was in turn caused by a reaction to an injection of the Pfizer vaccine on December 18, 2020. Pfizer replied "we don't believe at this time that there is any direct connection to the vaccine.”(1) They also insisted there is no indication that the vaccine could be connected to thrombocytopenia. Notice “an idiopathic disease is any disease with an unknown cause or mechanism of apparent spontaneous origin.”(2) If we are right, Dr. Micheal did not die of anything “ideopathic” at all.
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With the help of information from the doctors4covidethics and Wikipedia, I will explain the connection between the Pfizer mNRA vaccine and Dr. Michael’s death from Idiopathic Thrombocytopenic Purpura.(3) I claim no originality for this account. My goal is only to show how others understand what Pfizer does not want to understand, the way that their medication can kill healthy people. The passages from Wikipedia are used to unpack some of the central concepts of microbiology which may be unfamiliar to most of us who do not have an extensive scientific training.
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HOW AN mRNA VACCINE WORKS
We must begin with a description of how an mRNA vaccine works. This account is taken from a website of the Center for Disease Control, the CDC.
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"COVID-19 mRNA vaccines give instructions for our cells to make a harmless piece of what is called the “spike protein.” The spike protein is found on the surface of the virus that causes COVID-19.
COVID-19 mRNA vaccines are given in the upper arm muscle. Once the instructions (mRNA) are inside the immune cells, the cells use them to make the protein piece. After the protein piece is made, the cell breaks down the instructions and gets rid of them.
"Next, the cell displays the protein piece on its surface. Our immune systems recognize that the protein doesn’t belong there and begin building an immune response and making antibodies, like what happens in natural infection against COVID-19.
"At the end of the process, our bodies have learned how to protect against future infection. The benefit of mRNA vaccines, like all vaccines, is those vaccinated gain this protection without ever having to risk the serious consequences of getting sick with COVID-19."(4)
.
IMAGE FROM WIKIPEDIA(5)

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The “spike protein” is a central actor in the new COVID-19 medications. It is a small part of the virus that causes COVID-19. The basic idea is to help our immune system to protect us against future infection.  This is why it is called a vaccine, even though the method of helping the immune system is completely new and not tested for the usual 5 to 15 years.
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The “immune cells” in the description above are known as Dendritic cells. "Their main function is to process antigen material and present it on the cell surface to the T cells of the immune system."(6) Other cells in the body "can potentially absorb vaccine mRNA, manufacture spikes, and display spikes on their surfaces, however dendritic cells absorb the mRNA globules much more avidly."(7)
"Once the viral antigens are produced by the host cell, the normal adaptive immune system processes are followed. Antigens are broken down by proteasomes, then class I and class II MHC molecules attach to the antigen and transport it to the cellular membrane, 'activating' the dendritic cell. Once the dendritic cells are activated, they migrate to lymph nodes, where the antigen is presented to T cells and B cells.This eventually leads to the production of antibodies that are specifically targeted to the antigen, resulting in immunity."(8)
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SECOND COMMENT BY DOCTORS4COVIDETHICS
In their open letter, the doctors4covidethics begin by pointing out that “following intramuscular injection, it must be expected that the gene-based vaccines will reach the bloodstream and disseminate throughout the body.”(9) This is their next point:
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“2. It must be expected that the vaccines will remain entrapped in the circulation and be taken up by endothelial cells. There is reason to assume that this will happen particularly at sites of slow blood flow, i.e. in small vessels and capillaries.”
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So what are endothelial cells?
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“Endothelial cells line the interior surface of blood vessels, and lymphatic vessels. The endothelium forms an interface between circulating blood or lymph in the lumen and the rest of the vessel wall. Endothelial cells are the primary cell type which contacts blood and are responsible for hemostasis and blood fluidity by preventing platelet aggregation and thrombosis.”(10)
“Thrombosis is the formation of a blood clot inside a blood vessel, obstructing the flow of blood through the circulatory system.”(11)
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FOURTH COMMENT BY DOCTORS4COVIDETHICS
In the previous point doctors4covidethics anticipate that the nanoparticles in the mRNA vaccines will damage the endolthelial cells by being taken up by them. This is their next point:
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“4. It must be expected that endothelial damage with subsequent triggering of blood coagulation via platelet activation will ensue at countless sites throughout the body.”
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This process of coagulation via platelet activation is explained in the following passage:
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“Coagulation begins almost instantly after an injury to the endothelium lining a blood vessel. Exposure of blood to the subendothelial space initiates two processes: changes in platelets, and the exposure of subendothelial tissue factor to plasma factor VII, which ultimately leads to cross-linked fibrin formation. Platelets immediately form a plug at the site of injury; this is called primary hemostasis. Secondary hemostasis occurs simultaneously: additional coagulation (clotting) factors beyond factor VII respond in a cascade to form fibrin strands, which strengthen the platelet plug. Disorders of coagulation are disease states which can result in problems with hemmorhage, brusing, or thrombosis.”(12)
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FIFTH COMMENT BY DOCTORS4COVIDETHICS
“5. It must be expected that this will lead to a drop in platelet counts, appearance of D-dimers in the blood, and to myriad ischaemic lesions throughout the body including in the brain, spinal cord and heart. Bleeding disorders might occur in the wake of this novel type of DIC-syndrome including, amongst other possibilities, profuse bleedings and haemorrhagic stroke.”
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“A lesion is any damage or abnormal change in the tissue of an organism.”(13)
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“Ischemia is a restriction in blood supply to tissues, causing a shortage of oxygen that is needed to keep tissue alive.”(14)
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So “myriad ischaemic lesions throughout the body” means many kinds of tissue damage caused by an inadequate supply of blood.
“Haemorrhagic stroke is a sudden bleeding into the tissues of the brain.”(15)
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“D-dimer is a fibrin degradation product, a small protein fragment present in the blood after a blood clot is degraded by fibrinolysis. D-dimers are not normally present in human blood plasma, except when the coagulation system has been activated, for instance because of the presence of thrombosis tor disseminated intravvascular coagulation.”(16)
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“Disseminated intravascular coagulation (DIC) is a condition in which blood clots form throughout the body, blocking small blood vessels. Symptoms may include chest pain, shortness of breath, leg pain, problems speaking, or problems moving parts of the body. As clotting factors and platelets are used up, bleeding may occur. This may include blood in the urine, blood in the stool, or bleeding into the skin. Complications may include organ failure.”(17)
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SIXTH COMMENT BY DOCTORS4COVIDETHICS
“6. The SARS-CoV-2 spike protein binds to the ACE2 receptor on platelets, which results in their activation [6]. Thrombocytopenia has been reported in severe cases of SARS-CoV-2 infection [7]. Thrombocytopenia has also been reported in vaccinated individuals [8].”
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“Thrombocytopenia is a condition characterized by abnormally low levels of platelets, also known as thrombocytes, in the blood.”(18)
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This is a quote from footnote [6] in the above passage which explains what “platelet activation” means.
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“Spike protein directly stimulated platelets to facilitate the release of coagulation factors, the secretion of inflammatory factors, and the formation of leukocyte–platelet aggregates.”(19)
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In other words, the COVID-19 spike protein – which the mRNA vaccines via their nanoparticles introduce into the blood stream – causes coagulation in the blood vessels. This in turn reduces the number of platelets in the circulatory system. Remember with Disseminated intravascular coagulation clotting factors and platelets can be used up.
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SO WHAT DOES THIS ADD UP TO?
After an mRNA vaccination, the nanoparticles containing the spike protein will travel throughout the body. The nanoparticles in the circulatory system will be taken up by and damage the endothelial cells which line the inside of blood vessels. The damage to the endothelial cells will cause blood coagulation as the platelets are activated. The coagulaltion will cause the number of platelets to decline as they are incorporated into the blood clots. As a result there will be many kinds of tissue damage caused by an inadequate supply of blood. There could also be profuse bleeding and sudden bleeding into the brain.
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Their final point is that abnormally low levels of platelets in the circulatory system (Thrombocytopenia) is also caused by severe cases of SARS-CoV-2 infection. Thus the spike protein can cause the same damage no matter how it enters the blood system, whether by SARS-CoV-2 infection or by an mNRA vaccine.
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This is also the view of Hamid Merchant, Subject Leader in Pharmacy, University of Huddersfield. In a paper published on the 15th of March, 2021, he writes:
.
“In author’s opinion, it is plausible that CoViD genetic vaccines may have a direct role in spurring autoimmune response against platelets that may clinically manifest in thrombocytopenia, haemorrhage, and blood clots.”(20)
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WHAT DO WE FIND IN THE REPORTS OF ADVERSE REACTIONS?
According to the “COVID-19 mRNA Pfizer- BioNTech vaccine analysis print” updated on the 18th March 2021, there were 11 cases of Immune Thrombocytopenia and 13 cases of Thrombocytopenia with one death from the latter.(21)
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The following report comes from the USA:
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“By the end of January, 32 cases of a decreased platelet count, 14 cases of thrombocytopenia, and 11 cases of immune thrombocytopenia were recorded in people who had received either Pfizer or Moderna COVID vaccines in the U.S.”(22)
.

.
At this point we need to look at the death of a Florida doctor Gregory Michael MD. This is part of the report by his wife, Heidi Neckelmann:
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"He was vaccinated with the Pfizer vaccine at MSMC on December 18, 3 days later he saw a strong set of petechiae (dots on your skin which are a sign of blood leaking from capillaries under your skin) on his feet and hands which made him seek attention at the emergency room at MSMC. The CBC that was done at his arrival showed his platelet count to be 0 (A normal platelet count ranges from 150,000 to 450,000 platelets per micro liter of blood.) He was admitted in the ICU with a diagnosis of acute ITP (Idiopathic Thrombocytopenic Purpura, a rare autoimmune disorder that causes low platelet levels) caused by a reaction to the COVID vaccine."(23)
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Dr Michael first experienced blood leaking from capillaries under his skin. This was described by the doctors4covidethics as “endothelial damage with subsequent triggering of blood coagulation via platelet activation will ensue at countless sites.” Next it was found that he had a zero platelet count. This was fully expected by the doctors4covidethics: “It must be expected that this will lead to a drop in platelet counts,” just what results from Thrombocytopenia.
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I don’t believe Pfizer, governments, the media or even most people who discuss these new vaccines recognize that now there is a plausible explanation for the death of Dr. Michael supplied by the doctors4covidethics, the burden of proof now lies with Pfizer to prove that this causal explanation is incorrect. What have we missed?

FOOTNOTES
3. I have also had invaluable assistance from Dr Ah Kahn Syed  @arkmedic
19. "SARS-CoV-2 binds platelet ACE2 to enhance thrombosis in COVID-19"; https://jhoonline.biomedcentral.com/articles/10.1186/s13045-020-00954-7
20. "CoViD Vaccines and thrombotic events: Possibility of mRNA translation and spike protein synthesis by platelets?"; https://www.bmj.com/content/372/bmj.n699/rr-6

Some Side Effects Are Not A Coincidence: mRNA COVID-19 Vaccines Cause Lymphadenopathy

INTRODUCTION
On February 28, 2021 a letter entitled "Urgent Open Letter from Doctors and Scientists to the European Medicines Agency regarding COVID-19 Vaccine Safety Concerns” was released.(1)  Calling themselves Doctors4covidethics, they expressed grave concerns about gene-based COVID-19 vaccines. They raise three different issues of principle:
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1. Many side effects of these vaccines have appeared in previously healthy young people.
2. There have been many reports of people in care homes being infected by Covid-19 after they have been vaccinated.
3. We have some doubt that key issues about the safely of these vaccines were adequately examined before their approval.

They also demanded that the European Medicines Agency provide additional evidence on seven different points. In conclusion they state that "the approval of the COVID-19 vaccines by the EMA was premature and reckless, and the administration of the vaccines constitutes 'human experimentation', which is in violation of the Nuremberg Code." Finally they demand "that approval for use of the gene-based vaccines be withdrawn until all the seven issues have been properly addressed by the exercise of due diligence by the EMA."
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In what follows, with the help of the doctors4covidethics and Wikipedia, I will show how one of the seven points raised in their letter can give us a cogent explanation of one of the common side effects listed in the UK’s Case Series Drug Analysis, Lymphadenopathy.(2) Once we understand how an mRNA vaccine works, and examine points 1. and 3. in their letter, it will be obvious that the observed cases of Lymphadenopathy are directly caused by the administration of an mRNA vaccine.
.
.
HOW AN mRNA VACCINE WORKS
We must begin with a description of how an mRNA vaccine works. This account is taken from a website of the Center for Disease Control, the CDC.
.
"COVID-19 mRNA vaccines give instructions for our cells to make a harmless piece of what is called the “spike protein.” The spike protein is found on the surface of the virus that causes COVID-19.
COVID-19 mRNA vaccines are given in the upper arm muscle. Once the instructions (mRNA) are inside the immune cells, the cells use them to make the protein piece. After the protein piece is made, the cell breaks down the instructions and gets rid of them.
"Next, the cell displays the protein piece on its surface. Our immune systems recognize that the protein doesn’t belong there and begin building an immune response and making antibodies, like what happens in natural infection against COVID-19.
"At the end of the process, our bodies have learned how to protect against future infection. The benefit of mRNA vaccines, like all vaccines, is those vaccinated gain this protection without ever having to risk the serious consequences of getting sick with COVID-19."(3)

IMAGE FROM WIKIPEDIA(4)
The “immune cells” in the description above are known as Dendritic cells. "Their main function is to process antigen material and present it on the cell surface to the T cells of the immune system."(5) Other cells in the body "can potentially absorb vaccine mRNA, manufacture spikes, and display spikes on their surfaces, however dendritic cells absorb the mRNA globules much more avidly.(6)
"Once the viral antigens are produced by the host cell, the normal adaptive immune system processes are followed. Antigens are broken down by proteasomes, then class I and class II MHC molecules attach to the antigen and transport it to the cellular membrane, 'activating' the dendritic cell. Once the dendritic cells are activated, they migrate to lymph nodes, where the antigen is presented to T cells and B cells.This eventually leads to the production of antibodies that are specifically targeted to the antigen, resulting in immunity."(7)
.
.
THE mRNA VACCINES CAUSES AN AUTOIMMUNE RESPONSE
This is the first comment on mRNA vaccines in the letter from the doctyors4covidethics:
.
1. Following intramuscular injection, it must be expected that the gene-based vaccines will reach the bloodstream and disseminate throughout the body [1].
.
In their second comment they discuss the effect this will have on endothelial cells, but this will be discussed in another article.This is the third comment:
.
It must be expected that during expression of the vaccines’ nucleic acids, peptides derived from the spike protein will be presented via the MHC I — pathway at the luminal surface of the cells. Many healthy individuals have CD8-lymphocytes that recognize such peptides, which may be due to prior COVID infection, but also to cross-reactions with other types of Coronavirus.[3; 4] [5]. We must assume that these lymphocytes will mount an attack on the respective cells.
.
In the account given by the CDC, the nanoparticles in the vaccine will enter and be processed by the dendritic cells. Then the “cell displays the protein piece [it has created from the nanoparticle] on its surface. Our immune systems recognize that the protein doesn’t belong there and begins building an immune response and making antibodies...” A passage from Wikipedia explains this process as follows: “Once the dendritic cells are activated, they migrate to lymph nodes, where the antigen is presented to T cells and B cells.”(8)
.
But the doctors4covidethics explain that many people will have been exposed to COVID or other types of Coronavirus. This means that the “spike” protein (made up of long chains of amino acids) which occurs on all coronavirus or peptides (smaller chains of amino acids) which are parts of the spike protein, will be recognized as belonging to a pathogen. Thus when the dendritic cell displays “the protein piece” created from the vaccine’s nanoparticle the immune system will not “begin to build an immune response and make antibodies...” or just “migrate to the lymph nodes”. Instead, since the dendritic cell displays a protein piece created from the vaccine nanoparticle, it will be attacked by the CD8-lymphocytes that recognize such peptides as pathogens.
.
We can see that in the story the CDC tells assumes nobody has been exposed to COVID or any other types of Coronavirus. They assume the immune system is ignorant of the threat of COVID, and the mRNA vaccine is going to teach the immune system to be prepared to attack it. But introducing the spike protein will not "teach" the immune system anything if a person has had some previous exposure to any type of Coronavirus. The cell which displays the recreated spike protein will be attacked because it has already been recognized as a pathogen and the immune system via the CD8-lymphocytes will destroy it.
.
We should note that in the COVID-19 mRNA Pfizer- BioNTech vaccine analysis print of March 9th, 2021 from the UK’s Case Series Drug Analysis, there are 1973 reports of Lymphadenopathy and 266 reports of Lymph node pain.(9)
.
Lymphadenopathy is considered to be a nonmalignant hyperimmune reaction to chronic antigenic stimuation; there is proliferation of B cells accompanied by profound deficiency of T cells.”(10)
Lymphadenopathy is a common and nonspecific sign. Common causes include infections (from minor ones such as the common cold to serious ones such as HIV/AIDS), autoimmune diseases, and cancers.” (11)
Basic B cell function: bind to an antigen, receive help from a cognate helper T cell, and differentiate into a plasma cell that secretes large amounts of antibodies.”(12)
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So what’s going on in the lymph nodes? There is a hyperimmune reaction to chronic antigenic stimuation, autoimmune activity, and the secretion of large amounts of antibodies. Isn’t this just what the doctors4covidethics describe in their third comment?
.
In the COVID-19 mRNA Pfizer- BioNTech vaccine analysis print of March 9th, 2021 we can also find 437 cases of COVID-19 reported as a possible adverse event with 22 deaths from this infection and 415 cases of influenza. It has been suggested that the mRNA vaccines actually shut down the immune system and we have just seen how this can happen. Since the immune system is overloaded by an attack on the cells producing the viral particles, it is in efffect unable to deal with other pathogens which happen to be present. This might explain why a medication that is supposed to protect us from COVID-19 infection sometimes allows this infection or an influenza to take hold. In cases where the person has already been exposed to COVID-19 or another Coronavirus, the mRNA medication interferes with the normal action of the immune system so a person can no longer fight off other pathogens.
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Finally, if the doctors4covidethics are explaining that the immune system will attack the cells producing the viral particles. then they will attack the body's own cells, as in rheumatoid arthritis or any autoimmune disease. So the mRNA vaccines cause an autoimmune response under certain conditions which are by no means rare.
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Some might object that lymphadenopathy is not a serious problem for mRNA vaccines because it is "just" lymphadenopathy, which is transient. If this was the only problem, those who don't experience lymphadenopathy might be inclined to think it is of no imtportance. However this ignores the situation described by the doctors4covidethics in their first point.  The nanoporticles in the injection "disseminate throughout the body". In other words, for people who have been exposed to COVID-19 or any other type of Coronavirus, their immune system is already set to attack the activated dendritic cells showing the antigen derived from the nonoparticle. Since the nanoparticles are disseminated throughout the body, they will be attacked anywhere they can be found. The vaccine does not work to destroy any COVID-19 virus, it works to mobilize the immune system to attack the dendritic cells that are modified by the nanoparticles. And I have argued that this complete focus on the newly created dendritic cells means that the person can be infected by any other pathogen that happens to be present.
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FOOTNOTES FOR DOCTORS4COVIDETHICS LETTER
[1] Hassett, K. J.; Benenato, K. E.; Jacquinet, E.; Lee, A.; Woods, A.; Yuzhakov, O.; Himansu, S.; Deterling, J.; Geilich, B. M.; Ketova, T.; Mihai, C.; Lynn, A.; McFadyen, I.; Moore, M. J.; Senn, J. J.; Stanton, M. G.; Almarsson, Ö.; Ciaramella, G. and Brito, L. A.(2019).Optimization of Lipid Nanoparticles for Intramuscular Administration of mRNA Vaccines, Molecular therapy. Nucleic acids 15 : 1–11.
[2] Chen, Y. Y.; Syed, A. M.; MacMillan, P.; Rocheleau, J. V. and Chan, W. C. W.(2020). Flow Rate Affects Nanoparticle Uptake into Endothelial Cells, Advanced materials 32 : 1906274.
[3] Grifoni, A.; Weiskopf, D.; Ramirez, S. I.; Mateus, J.; Dan, J. M.; Moderbacher, C. R.; Rawlings, S. A.; Sutherland, A.; Premkumar, L.; Jadi, R. S. and et al.(2020). Targets of T Cell Responses to SARS-CoV-2 Coronavirus in Humans with COVID-19 Disease and Unexposed Individuals, Cell 181 : 1489–1501.e15.
[4] Nelde, A.; Bilich, T.; Heitmann, J. S.; Maringer, Y.; Salih, H. R.; Roerden, M.; Lübke, M.; Bauer, J.; Rieth, J.; Wacker, M.; Peter, A.; Hörber, S.; Traenkle, B.; Kaiser, P. D.; Rothbauer, U.; Becker, M.; Junker, D.; Krause, G.; Strengert, M.; Schneiderhan-Marra, N.; Templin, M. F.; Joos, T. O.; Kowalewski, D. J.; Stos-Zweifel, V.; Fehr, M.; Rabsteyn, A.; Mirakaj, V.; Karbach, J.; Jäger, E.; Graf, M.; Gruber, L.-C.; Rachfalski, D.; Preuß, B.; Hagelstein, I.; Märklin, M.; Bakchoul, T.; Gouttefangeas, C.; Kohlbacher, O.; Klein, R.; Stevanović, S.; Rammensee, H.-G. and Walz, J. S.(2020). SARS-CoV-2-derived peptides define heterologous and COVID-19-induced T cell recognition, Nature immunology.
[5] Sekine, T.; Perez-Potti, A.; Rivera-Ballesteros, O.; Strålin, K.; Gorin, J.-B.; Olsson, A.; Llewellyn-Lacey, S.; Kamal, H.; Bogdanovic, G.; Muschiol, S. and et al.(2020). Robust T Cell Immunity in Convalescent Individuals with Asymptomatic or Mild COVID-19, Cell 183 : 158–168.e14.
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Dr Tenpenny Explains A Serious & Potentially Deadly Side Effect Of mRMA Vaccines

Dr Sherri Tenpenny, an American board-certified doctor who has researched vaccines for four decades, has warned of an extremely serious and potentially deadly side effect of mRNA vaccines – they can destroy the body’s natural healing process by killing cells called type 2 macrophages. Dr Tenpenny can be seen on the video below speaking with Californian activist Reinette Senum.

EXPLAINS HOW THE DEPOPULATION MRNA VACCINES WILL START WORKING IN 3-6 MONTHS


The Free Dictionary describes macrophages as “a type of white blood cell that engulfs and digests cellular debris, foreign substances, microbes, cancer cells, and anything else that does not have the types of proteins specific to healthy body cells on its surface in a process called phagocytosis. These large phagocytes are found in essentially all tissues, where they patrol for potential pathogens by amoeboid movement.”

In other words, these cells are an important part of your body’s ability to fight and heal disease and infections. The destruction of type 2 macrophages by coronavirus vaccines was observed in a study cited by Dr Tenpenny at this website https://vaxxter.com/covid-vaccines-part-2/ and was the primary reason for the abandonment of trials of previous coronavirus vaccines from around 2002.

Dr Tenpenny predicts the same process will be triggered in people vaccinated with the latest coronavirus vaccines when they encounter seven of 36 wild coronaviruses that existed long before COVID-19. She explains (from the 17-minute mark in the video) that there are two types of macrophages – the first creates an inflammatory response to attack infection and the second an anti-inflammatory response to “clean up the mess”.

She says the genetically engineered antibodies generated by these mRNA vaccines to attack the COVID-19 spike protein (the central purpose of the vaccines) kills the type 2 macrophages by attaching themselves to the macrophage cells and inactivating them.

This had been demonstrated in the animal testing for coronavirus vaccines going back to 2002 when animals died from their lungs filling up with the inflammatory type 1 macrophages. Unvaccinated test animals given the same infection had both type 1 and 2 macrophages in their lungs.

The implications of this are horrific, namely a wave of autoimmune diseases in the population and an impaired ability to have children – but of course, as Dr Tenpenny notes, big pharma will have all sorts of drugs to sell to address the problem. “Some people are going to die from the vaccine directly but a large number of people are going to get horribly sick and get all kinds of auto-immune diseases 42 days to maybe a year out,” she told Californian interviewer Reinette Senum.

She further fears that uninformed doctors and others will attribute these delayed side effects to virus mutations and urge further mRNA shots. Never underestimate human stupidity. Please share this article and the video interview link.

Dr Tenpenny recommends reading and studying the 2019 study by Liu, Li et al, “Anti-spike IgG antibody causes severe acute lung injury by skewing macrophage responses during acute SARS-CoV infection." A link to this article is given below. Further details of Dr Tenpenny’s research can be found at Vaxxter.com.