To those of us well-versed in the biology and emerging safety data relating to the injections referred to as ‘Covid vaccines’, what is playing out before us is like a slow-motion motorway pile-up: we can see it unfolding, causing immense harm, have no idea when it will stop, and feel powerless to do much about it.
At present, it is unknown for how long this ghastly experiment will continue and how much further harm will be caused.
However, unfortunately there are reasons to believe the following may well be the case:
- It will take much longer for the harms caused to be acknowledged by the ‘establishment’ and so the injections will continue to be administered for some time yet – albeit to smaller and smaller groups as time progresses, and with varying degrees of enthusiasm in different locations.
- Even if the injections were to stop now, it is unknown how much the harms caused thus far have actually come to light, and how much may manifest over the ensuing years or even decades.
One category of reasons for the above is essentially political. We are referring here to the complete failure on the part of those we previously relied upon to ensure pharmaceutical interventions are safe. The reasons for this are willful blindness on the part of our regulatory authorities, combined with with the by now rather obvious capture of these institutions by two different interested parties:
- Politicians who will apparently stoop to anything, including installing transnational coordinated censorship regimes, to keep their monumental errors hidden;
- Big Pharma, desperate to ensure that its bonanza continues as long as possible.
But as well as the above there are some inherent biological reasons which may hinder and delay the ending of this unprecedented catastrophe.
For a variety of reasons which are listed below, many uncertainties remain concerning the biological action of repeated doses of the mRNA products. However, what is known suggests that many of the harms they cause are mediated by inflammatory and autoimmune processes induced (potentially) throughout the body.
To recap the principal mode of action, the lipid nanoparticles carry mRNA into some of the recipient’s cells. These cells express spike protein, which is foreign to the body. The body’s immune system creates antibodies to that protein, as well as attacking and destroying the cells which express the protein.
In contrast to the original claims made – that the product would be broken down in the deltoid (shoulder) muscle with little or no distribution throughout the body, it turns out that the product does become widely distributed – potentially to every organ system. Of course, this should not have been surprising, since the whole point of the lipid in the lipid nanoparticles is to make them able to cross membranes and become distributed, to help with their original role as conveyors of targeted drugs to cancerous cells.
Moreover:
- The amount of spike protein produced is uncontrolled and uncontrollable, as is the duration over which it is produced. High levels of spike antibodies have been found many months after injection, suggesting continued creation of the protein.
- The spike protein produced has inbuilt differences compared to the natural version – the replacement of uridine by pseudouridine – designed to ensure the mRNA is less degradable. Other changes (e.g. codon optimisation) may well alter the folding characteristics of the protein produced, with unknown consequences.
- It is thought that the spike protein may translocate to the nuclei of cells, the risks of which are still unknown.
- The repeated creation of spike from multiple injections may have deleterious effects, both on the ability to fight similar viruses (so-called ‘tolerance‘ created through changing the type of antibody created) through to immune exhaustion (reducing the body’s ability to fight other pathogens or cancers).
- The LNPs themselves (notwithstanding their ‘payload’) may well be pro-inflammatory in themselves.
- The significance of above-tolerance levels of DNA contamination left-over from the bacterial plasmids used in the high-volume manufacturing process are as yet unknown.
Much of the harm observed appears to be inflammatory or autoimmune in nature. Both these processes are usually chronic, not acute problems. It is perfectly possible that once started, they continue for months or even years. Notably, chronic inflammation is thought to have a central role in many of the chronic pathologies increasingly suffered by Westerners over the past few decades.
Hence the tail of visible harm could manifest over a long timeframe. Moreover, because chronic inflammatory and autoimmune processes, by their nature, build slowly over time, the individual is likely to become habituated to ill effects, until a critical event occurs after some longer period.
A good example of this is with coronary artery disease. It is thought that inflammation is an important part of the pathophysiology in which a ‘plaque’ builds up in the arterial wall. This may be asymptomatic until it ruptures causing a total blockage resulting in a ‘heart attack’. If the injections are accelerating this inflammatory process, the course of the pathological process may appear identical to that previously seen in many people, although it has been brought on and accelerated beyond what that person would otherwise have experienced; however, because it is within the range of possible or even probable illnesses observed, it gets dismissed as ‘one of those things’.
Cigarette manufacturers used to deny their products caused lung cancer by pointing out non-smokers who suffered the same fate. It was, in fact, only by rigorous epidemiological analysis that the link could be unequivocally proven. For the Covid injections, it is deeply concerning that authorities seem to be doing everything possible to hinder access to the data which would permit such analyses to be performed.
Another reason why harms may be difficult to identify is that in some cases the pathological processes may be merely reducing physiological reserve, something which can go unnoticed for years or decades. Most of the body’s systems have significant inbuilt redundancy, which is why a kidney, or a significant part of the liver, can be lost while still maintaining good physiological and biochemical control. But if someone loses a kidney, they are more likely to suffer renal failure as they get older and the efficiency of their kidneys declines, and the available reserve falls away. Likewise, if part of the heart is damaged when young (e.g. through myocarditis), the person may well make a full recovery in the short term in the sense of being physiologically normal, but be more vulnerable to suffering from heart failure (where the heart can’t pump blood around the body sufficiently) after losing some more heart muscle tissue after – say – a heart attack in middle age.
Finally, it should be noted that because of the wide distribution throughout the body (something rather obvious given the wide range of reports in the various adverse event databases), the harms appear to be manifesting in an extremely wide variety of symptoms and disorders. These will be problematic to diagnose, requiring lengthy and complex investigation, with multiple pathologies being possible. Such profiles of types of harms have not generally been observed with pharmaceutical products before; in most cases, the adverse effects are more limited in scope, and more closely temporally related to dosing (though there are some exceptions).
In conclusion, it is not possible to say whether we are at the beginning, or near the end of, the harms caused by these agents.
A combination of what may be termed ‘political’ reasons, together with the inherent biological characteristics of the mRNA ‘vaccines’, all mitigate against the injections being identified and accepted anytime soon as being the causative agent of significant and sustained harms being experienced by an unacceptably large number of people.
Moreover, it remains likely that they will continue to be administered for some time yet – at least to certain groups in certain places – prolonging and exacerbating the harms already caused.
Dr. Jonathan Engler is Co-Chair of the HART group, which first published this article. Subscribe to the HART Substack.
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