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Guy Hatchard
Guy Hatchardhttps://hatchardreport.com/
Guy Hatchard PhD is a statistician and former senior manager at Genetic ID, a global food safety testing and certification laboratory. Guy's book 'Your DNA Diet' is available on Amazon.com.

Guy Hatchard: Is the spike protein causative in haemoglobin disorders and clotting?

What are the wider implications for personal health, pandemic policy and mitigation strategies?

For some time there have been anecdotal reports circulating concerning the appearance and formation of unusual rubbery blood clots which have been detected in Covid vaccinated individuals who have died. Some embalmers, pathologists, and funeral home directors have noted extensive white proteinous fibrous structures blocking arteries, unique in their experience, which may have played a role in the etiology and pathology of fatal illness. 

If you have been following the issue, you will have seen photographs and/or videos of these structures like this short video from a concerned British funeral home owner, or you might have heard senior US pathologist Dr Ryan Cole discuss the phenomenon. 

This issue is contentious and the subject of sceptical comment from some quarters, but the record number of unexplained deaths, even among the young, and the relentless and reckless promotion of mRNA vaccines points to a need for closer investigation.

Dr Jessica Rose, a postdoc biochemist, who blogs on Substack and podcasts on Audible, has released a probing scientific analysis of the possible causes of this widely recognised clotting phenomenon under the title “Is the spike protein acting as a prion with regard to haemoglobin molecules? And is porphyria being induced?. This article is both highly technical and partly speculative, but it is worth extracting some of the take home warnings and conclusions.

First of all note that this is the kind of precautionary post trial analysis that was omitted by Pfizer and others as they rushed mRNA vaccines to market. The reason behind 10 year approval cycles for previous vaccines is precisely because unexpected effects in the vaccine research field are the norm rather than the exception. The introduction of biotech jabs should have raised red flags about the short trial time frames, but it didn’t.

Dr Rose examines the possibility that the Covid mRNA vaccination causes haemolysis (rupture of red blood cells) releasing massive amounts of haemoglobin. And then asks: does the spike protein, due to its amyloidogenic peptides, trigger misfolding of the haemoglobin into amyloid fibrils causing subsequent blood clots and oxygen incapacity?

In other words, does the spike protein have prion-like properties that are causing chain clotting reactions (including microclots) which can cause death? Dr Rose thinks the answer to this question is a ‘YES’ and calls for more research to investigate the phenomenon.

Prions are pathogens that cause disease because of their misfolded shape rather than their biology. Misfolded proteins do not function like their correctly folded cousins and they are associated with neuro-degenerative diseases like Alzheimer’s disease. Prions can transform or ‘teach’ other proteins to misfold. It’s not really teaching as much as the disallowance of proper folding in adjacent proteins which then spreads further. 

Disease-causing prions can resist proteolysis – the process which under normal conditions removes misfolded proteins. Protected from correction, prions can initiate an autocatalytic chain reaction which forms alien obstructive structures in the physiology. In Mad Cow Disease for example a prion chain reaction progressively replaces healthy structures in the brain. 

Dr Rose outlines a plausible chain of events in the blood along with supporting evidence from VAERS data. According to Dr. Rose, reported incidence of porphyria, a rare disease normally caused by genetic defects, has increased in VAERS data by 17,265% when compared to years prior to the introduction of mRNA vaccination. 

Porphyrins play a key role in the chain of reactions that produce haemoglobin. Porphyria is an accumulation of porphyrins in the liver or bone marrow due to defects in the porphyrin development pathway. 

In addition to a wide range of severe physical and mental symptoms, porphyria can be associated with haemoglobin instability. Rupture of red blood cells is a necessary precondition for the release of unstable haemoglobin proteins susceptible to misfolding.

The increased incidence of porphyria raises another important safety issue which has consistently dogged the introduction of new drugs, vaccines, and even novel food ingredients. There is often an underlying assumption that chemical, physiological, biological, or genetic components perform single functions in isolation. This is invariably incorrect. Most have multiple roles. Altering one function, in the hope of correcting a single imbalance, can affect a whole range of other systems and outcomes.

Acute porphyria, in addition to physical symptomatology such as abdominal pain, has a psychiatric manifestations include hysteria, anxiety, depression, phobias, psychosis, organic disorders, agitation, delirium, and altered consciousness ranging from somnolence to coma. Some patients develop psychosis similar to schizophrenia. All of these effects come down to a dysfunction in physical red blood cell formation.

As we have discussed previously, psychological effects of genetic and epigenetic interventions including mRNA vaccines remains a largely unexplored field, but not one where safety can be assumed a priori. Yet that is precisely what has happened. Absence of evidence (since no one has looked for or measured effects) is not evidence of absence. 

There is currently a lot of Covid hysteria, anxiety, agitation, and even phobia without much of a scientific or rational basis especially when you sit back and examine current Covid science publishing and data.

In summary, a whole range of naive safety assumptions have dogged the roll out of mRNA technology, and we have not yet adequately assessed the final outcomes of mRNA serious adverse effects.

Dr Rose raises a number of questions that require more investigation. Importantly, she urges extreme caution concluding:

Everyone needs to know why it’s essential not to introduce potential agents to disrupt the haemoglobin forming and clotting pathways [as the spike protein induced by mRNA vaccination does]. There are so many ways that things can go wrong. Which, is again, why I don’t understand why there are so many exceedingly arrogant humans who think it’s a good idea to mess with biology [using biotechnology].”

At the Hatchard Report we have already written about the persistence of the spike protein for months after mRNA vaccination and its capacity to accumulate in diverse organ systems. For this reason, it is clear that mRNA vaccine induced clotting can potentially affect all our organ systems in diverse areas of the physiology. The extent of this effect varies from individual to individual. There are currently inadequate procedures in the New Zealand health system to monitor such effects post vaccination or post mortem in order to investigate their extent more closely.

We started out by considering the causes of fibrous proteinous blood clots among the vaccinated, but by taking a wider angle of consideration we have realised that genetic interventions can threaten the holistic stability of life including even mental stability. Genetic structures connect mind and body. 

All-cause mortality has surged to unprecedented levels around the world initiating the sharpest fall in longevity in 100 years. There is really only one sensible course of action—an energetic multidisciplinary approach to assess the range of adverse effects of human genetic intervention. The effort should be aimed squarely at pausing biotech and finding mitigating health strategies. This will require open minds. Successful mitigation will have to identify, include, and encourage proven dietary and lifestyle initiatives. Carrying on with present policies regardless is not an option.

Which only leads us back to our very own incautious blinkered government, health advisors, and administrators who this week ramped up the advertising budget yet again to encourage second boosters for everyone and a fifth shot for those with immune deficiencies; completely ignoring accumulating evidence that mRNA vaccination itself causes immune deficiency, while boosters are associated with increased all-cause mortality.

Our government has also launched a new advertising campaign praising the recent closure of District Health Boards and the introduction of centralised control of medicine. According to the advertising campaign, there are now more opportunities for contactless virtual medical consultations. In other words, you don’t need to meet a doctor in person, you can get your medical help directly from…who?? Hopefully it’s not the central government. 

Guy Hatchard PhD was formerly a senior manager at Genetic ID a food testing and certification company (now known as FoodChain ID). Website: HatchardReport.com.

Guy is the author of ‘Your DNA Diet: Leveraging the Power of Consciousness To Heal Ourselves and Our World. An Ayurvedic Blueprint For Health and Wellness’.

The statements, views and opinions expressed in this column are solely those of the author and do not necessarily represent those of DTNZ.

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  1. MSM is already started spinning that the “lockdowns” are the main cause for excess deaths. Governments run by globalist agents, largely the West, are not going to implicate the mRNA jab at all. The so called experts hired by these governments are just propgandists or just after sponsored or funded health projects from Big Pharma and governments. Only some of the independent minded experts will expose the lies and the road to truth is going to be protracted and long. Even the Ivermectin Oxford trial was delayed and sabotaged. Only countries that not fully in the sphere of influence of US may do the right thing on researching the damaging effects of the jabs.


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