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Agreed. Cross-posted your comment to the Covid main thread.
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Until now, most of the public has accepted and supported the development of vaccines without doubt and hesitation. And rightly so, since vaccinations can save lives. But no vaccination will ever be perfect and free of side effects. Useful vaccines must meet two important requirements: 1. the vaccine must offer protection against a serious or even life-threatening disease; 2. its side effects must be within tolerable and acceptable limits. On balance, the benefit must be much greater than the risk. Sounds logical, doesn’t it?
And it is true. Who would get vaccinated against a common cold if this meant taking an incalculable risk of severe side effects? Furthermore, not every vaccination has to be useful for every person. Living in Germany, we do not need a vaccination against yellow fever, since it does not occur here.
We already know that COVID-19 puts a clearly defined group of people at risk – namely, those over 70 with serious preexisting conditions. For these people, vaccination against SARS-CoV-2 might possibly make sense. Of course, before such vaccinations could begin, the vaccine‘s efficacy and potential dangers would need to be examined very carefully. However, the clinical studies conducted thus far have excluded precisely this group of patients, so that efficacy and risks remained unknown before the roll-out of the vaccine.
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Is the mRNA vaccine dangerous?
"No" is the answer that is spread everywhere.
This is because 1) the vaccine introduces into our body only the information for a small part of the virus, for the so-called spike protein, which means that there is no intact virus that could propagate, and 2) the vaccine only imitates what Nature, too, would do. Intact viruses also release their genetic material into our cells when they attack, turning our cells into virus factories. So, no problem there at all, right?
Far from it.
A natural respiratory infection typically affects only the respiratory tract itself. If, at worst, cell death occurs, the damage is local and can be repaired relatively easily.
With a vaccine, however, the viral genetic information is injected into the muscle. Many believe that the packaged viral genes remain at the site of injection – that is, within in the muscle. The genes would be taken up by cells at the site, which is where most “virus factories” would be created. Side effects such as swelling, redness and pain at the injection site would be expected because of this, but they would remain relatively harmless and go away after a few days.
What a fatal mistake!
The virus genes in the Moderna and Biontech/Pfi-zer vaccines are packaged in so-called nanoparticles – which can be thought of as tiny packages, not made of paper, but of fat-like substances. This protects the contents and makes it easier for them to be absorbed by the cells of our body. The packaging itself causes a risk of severe allergic reactions that is many times higher than with conventional vaccines (20). It is thus not without reason that people with allergies are now being warned not to get vaccinated – life-threatening reactions (anaphylactic shock) could be triggered.
In fact, such dangerous side effects did occur in some vaccination volunteers, who required emergency treatment. In addition, nanoparticles can have numerous other harmful effects because they can interfere with the function of our blood cells and clotting system (21).
But it gets infinitely worse. It is part of basic medical knowledge that all soluble substances injected into muscle tissue enter the bloodstream and are distributed throughout the body within a very short time. This is precisely why substances that are supposed to act immediately are injected into the muscles. It is known that the injected gene packets also enter the bloodstream (22). Which cell types will take them up, process them, and then produce the virus protein? The answer to this is not known with certainty. We are now witnessing large-scale experiments on humans. This is absolutely irresponsible, especially since there was reason for caution from the beginning. The potential dangers from the “packaging” were already known. More significantly, however, alarming antibody-dependent enhancement – in this case, the antibodies do not prevent uptake of the virus into cells, but rather enhance it – has been observed in animal studies on SARS and other coronaviruses (23, 24).
In the decades-long, yet futile effort to develop vaccines against SARS or MERS, this enhancement effect was repeatedly observed, as one among problem among many others (25). With this in mind, should not animal studies have been conducted to clearly rule out this effect for SARS-CoV-2? Physicians who do not alert those willing to be vaccinated to the risk that vaccination could make the disease worse, not better, are in violation of their duty to inform (26). And more seriously, could the inoculation of viral genes trigger other novel immune-related enhancement effects? Shouldn’t such very elementary things have been considered and tested beforehand? As a reminder, lymphocytes have a long-term memory – they remember what the «molecular garbage« looks like that is produced in Coronavirus infections. And corona garbage looks pretty much the same no matter which member of the virus family it is derived from. All humans have had training rounds with coronaviruses, and thus they have lymphocytes that will recognize SARS-CoV-2 garbage. People without in-depth knowledge might counter that these cross-reactive killer lymphocytes were detected in only 40–70% of old blood samples, and they reacted only weakly against SARS-CoV-2 (27, 28). However, it is known that only a small proportion of all lymphocytes are in the blood at any given time. The others are just taking a break and resting in the lymphoid organs (including the lymph nodes).
Here, we note an exciting finding: In April 2020, Swedish researchers reported that they had discovered something truly remarkable. Activated and combat-ready T lymphocytes were found in the blood of all people (100%) infected with SARS-CoV-2, regardless of the severity of the disease (29). This finding is a clear, unmistakable warning. For context: during an initial confrontation of the immune system with a virus, the lymphocyte response will be sluggish. Rapid, strong reactions such as that documented by the Swedish team reveal that forewarned troops are already at the ready and can be mobilized on short notice. They will swarm out of the lymphoid organs to fight the enemy. Their main task: ex-termination of the virus factories – death to the body’s own cells that produce the virus particles. And now back to the new reality: the large-scale experiment on humans. The injected gene packets are taken up locally in muscle cells, but a large part reaches first the local lymph nodes and, after passing through these, the bloodstream. The lymph nodes are where the immune cell team resides. When the viral gene is taken up by any cell there, production of the spike protein gets underway. The corona killer lymphocyte next door wakes up and springs into action – the brotherly battle begins! Lymph node swelling. Pain. The lymphocytes psyche each other up and then emerge from the lymph nodes to seek out more enemies. Yes – over there – the muscle cells! There they are!!! Attack!!! At the injection site redness, swelling, bad pain. But now the nightmare. This is because the substances with small molecules – for example, blood sugar – can easily seep out of the blood into the tissue, whereas large molecules such as proteins cannot. For them, the vessel walls are tight thanks to the lining with a cell layer – the endothelial cells.
What are the gene packages like – large or small? Right – compared to blood sugar, they certainly are large. Therefore, once they enter the bloodstream, they will remain in the closed network of vascular tubes just like the blood cells. A small part of them is taken up by white blood cells. Presumably, however, most of the virus factories will be established in the endothelial cells, that is, in the innermost cell layer of the blood vessels themselves. This would happen mainly where the blood flows slowly – within the smallest and smallest vessels – because the gene packages can be taken up particularly efficiently by the cells there (30). The endothelial cells then produce the viral spike protein and place the waste at the door – on the side that faces the bloodstream, where killer lymphocytes are on patrol. This time, the fight is one-sided. The endothelial cells have no defense. What happens then can only be guessed at. Injury to the vascular lining usually leads to the formation of blood clots. This would likely happen in countless vessels in countless places in the body. If it happens in the placenta, severe damage to the child in the womb could result.Shudder. Is there evidence that something like this is taking place? Yes, there is talk of rare blood disorders in which a possible link to vaccination would have to be investigated (31). Strikingly, there are reports of patients in whom a sharp drop in blood platelets (thrombocytes) was observed. This would fit the hypothesis put forward here, because platelets are activated and used up at the sites of blood clot formation.
Could you check if the assumption is correct? Yes. Laboratory findings provide immediate information on whether blood clotting is underway. Autopsies could clarify whether clots have formed in the small vessels. And in the meantime, consideration could be given to whether anticoagulants should be administered to patients as a preventive measure. The administration of cortisone preparations to dampen lymphocyte activity might also be worth considering. There currently is a continuous stream of reports on deaths happening worldwide in close temporal connection with the vaccination. Officially it is said, of course, that the vaccination has nothing to do with these deaths. It is almost all older people with numerous preexisting conditions, who would have soon departed this world anyway. If that should be actually so, probably no thinking and sympathetic humans can fathom why these poor people still had to be inoculated with a poorly characterized vaccine such a short time before their natural deaths.What could cause death in a frail person hours or days after vaccination? Several effects are conceivable:
1. stress from the vaccination itself; allergic reactions.
2. autoimmune attack. Lymphocytes are also ope-rational in old age. In elderly people with preexisting disease, the attack on the virus factories could be the straw that breaks the camel’s back.
3. It becomes somewhat more complicated when a simultaneous infection with the SARS-CoV-2 also comes into play. In several nursing homes, there have apparently been COVID-19 outbreaks just in the days after residents were vaccinated. Funny, funny – up until that point, there had been hardly any cases in the en-tire area, and all hygiene measures had been followed.
There were outbreaks even after the second injection of the vaccine (32,33), a clear and expected indication that vaccination does not protect against infection.I think here one must distinguish between patients with an without preexisting latent infections – it is conceivable (though unlikely) that those without infection are protected, whereas those with the infection are killed. What is more, it seems that particularly the vaccinated are dying. Is this perhaps the immune-related exacerbation of diseases we have reason to fear? Not caused by antibodies, but by activated killer lymphocytes? And couldn’t this happen at any time to anyone vaccinated – tomorrow, the next day, next week, next fall? Because lymphocytes have an elephant’s memory. And they recognize something that looks similar in all coronaviruses: the molecular garbage that is produced by the virus-infected cells. That is, the lymphocyte-induced exacerbation of disease progression could arguably occur with any infection with a related virus. In any “successfully” vaccinated person – young or old – and at any time in the near or distant future.
Conclusion
Gene-based vaccines received emergency approval at lightning speed to combat a virus that is no more dangerous than influenza (34). There is now clear evidence that people can become severely ill and die from these vaccinations. No real-world benefit of vaccination has ever been shown. Until reliable and convincing data are available, this high-risk human experiment must not be allowed to continue.