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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.


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Explanation of Diagram: Shows a killer T cell attacking a cell infected with an unspecified antigen as part of the adaptive immune system. The infection of the cell (dendritic or B-cell) by the antigen produces antigen fragments (waste from absorbtion of the antigen) on the surface of the cell. This waste is shown in the diagram as a little red dot on the irregular blue infected cell. The killer T cell - shown as a blue circle at the top and bottom of the diagram - has a specialised antigen receptor, shown as the half-circle on the top of the T cell. This is specific to one kind of antigen, and when there is a match between the antigen waste - the red dot - and the receptor on the T cell, it releases cytokines (perforin and granulysin) which together will destroy the infected cell.
How this applies to cells which take up the nanoparticles with mRNA instructions: When lipid nanoparticles from the mRNA Covid-19 injections are taken up by endothelial cells (or any other cells), the cell will deposit the waste created from the process of producing a spike protein from the mRNA on its surface. When this waste is detected by killer T cells that have been exposed previously to Covid-19, some other coronavirus, or the mRNA produced spike protein itself, the cells showing the waste from the mRNA instructions will be attacked and destroyed by the appropriate killer T cells in the same way shown in the diagram.
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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. The other mechanism is explained above. When epithelial cells take up the genetic mRNA 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
Nausea
Vomiting
Blurred vision
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 experience them after Covid-19 injections, 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.

Another consequence of multiple blood clots in the circulatory system is known as Thrombocytopenia, an abnormally low level of platelets. As in the case of disseminated intravascular coagulation, the clotting removes the entire supply of platelets so blood can escape freely into any area it can, either as lilttle spots or bigger blotches. This means that in the worst cases, the mRNA injections can produce both blood clots and bleeding. (As a medical novice I find it hard to distinguish some cases of Thrombocytopenia from disseminated intravascular coagulation.)
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Thrombocytopenia
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Thrombocytopenia
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Adverse Events from Twitter
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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.
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