Thursday, 22 February 2024
Thursday, 25 August 2022
Graphene is being transmitted from the COVID Vaccinated to the Unvaccinated
Doctors discover Graphene is being transmitted from the COVID Vaccinated to the Unvaccinated, destroying Blood Cells & causing Blood Clots
In his latest set of slides of blood samples taken from both “vaccinated” and unvaccinated people, Dr. Philippe van Welbergen demonstrated that the graphene being injected into people is organising and growing into larger fibres and structures, gaining magnetic properties or an electrical charge and the fibres are showing indications of more complex structures with striations.
He also demonstrated that “shards” of graphene are being transmitted from “vaccinated” to vaccine-free or unvaccinated people destroying their red blood cells and causing blood clots in the unvaccinated.

Dr. Philippe van Welbergen (“Dr. Philippe”), Medical Director of Biomedical Clinics, was one of the first to warn the public of the damage being caused to people’s blood by Covid injections by releasing images last year of blood samples under the microscope.
At the beginning of July 2021, Dr. Philippe, was interviewed on a South African community channel, Loving Life TV. He explained that when his patients started complaining about chronic fatigue, dizziness, memory issues, even sometimes paralysis and late onset of heavy menstruation (women in their 60s upwards), he took blood samples. Their blood had unusual tube-like structures, some particles which lit up and many damaged cells. Few healthy cells were visible. Until three months earlier, he had never seen these formations in blood. We now know these tube-like structures are graphene.
Since then, Dr. Philippe has been a regular guest on Loving Life TV: blowing the whistle on the experimental Covid injection roll-out; providing updates on the increasing damage being done to blood by the experimental Covid injections over time; and, giving updates on the Covid situation in the UK and South Africa.
On 12 February 2022, Dr. Philippe returned again to Loving Life TV to release images of his latest slides of blood samples. The live stream was lengthy so Loving Life TV separated it into two parts.
Part One is a discussion including answers to the audience’s questions.
In Part Two, Dr. Philippe presents the images of his latest blood slides and explains what the images are showing. He discusses nearly 100 blood slides from both “vaccinated” and vaccine-free patients. His slides show that vaccine-free patients have been “infected with vaccine toxins through shedding.”
Below is a short clip from Part Two courtesy of The Timeline Post channel on Telegram.
Below is an image of typical healthy red blood cells as seen with a microscope, what blood should look like. There is no coagulation or foreign objects in it.

The next image is of a person who has been injected with the experimental Covid drug. The blood is coagulated, the misshapen red blood cells are clumped together. The cell encircled in the image is a healthy red blood cell, one of the few in the image, sitting alongside the graphene fibres. You can see the size of the graphene fibres in relation to the size of a red blood cell. Fibres of this size will block capillaries. You can also see the graphene fibres are hollow and contain red blood cells.

A couple of weeks before the video below was made, Dr. Philippe began noticing a magnetic or electrical polarity effect on different sides of the graphene fibres. In the image below, to the right of the fibre the cells are coagulated and on the left-hand side is what looks like a gap or roughly backwards “C” shaped spacing. Dr. Philippe says that this “behaviour” was not seen before but now, all of a sudden, it is being seen in almost every sample. It is an indication that “these things have changed, their reaction with surrounding blood cells has changed … and I don’t know what triggered it,” he said.

The image below is of a blood sample from a vaccine-free, or unvaccinated, three-year-old child. It shows pieces or “shards” of graphene that “are the result of shedding,” in other words the graphene has been transmitted from “vaccinated” parents to their unvaccinated child.

Below is the image of a blood sample from an eight-year-old unvaccinated child whose blood has been contaminated and destroyed by the transmission of graphene from those around him/her who have had a Covid injection. The child’s right arm and upper right leg are basically paralysed, the child is unable to lift his/her right arm and the thigh is not functioning properly.

Dr. Philippe’s presentation is truly eye opening and horrifying – a must watch, especially for those who proclaim Covid injections are “safe” and are insisting people be injected. The Covid injections are weapons of genocide and how the people who have designed them are still walking free is incredible.
You can either watch the presentation below or on Loving Life TV HERE.
Sunday, 21 August 2022
Mike Adams and Dr. Jane Ruby discuss the white embalmer clots
SHOCKING: White Embalmer Clots Are Self Assembling Circuits
NZ Herald rationalises the vaccination deaths
Fit and healthy Kiwis dying unexpectedly from mysterious adult condition
Every year, otherwise healthy New Zealanders drop dead with no warning. Researches hope new funding will prevent more deaths, writes health reporter Emma Russell.
Ifan Jones remembers kissing his 30-year-old wife goodbye and saying "I love you", as he did every morning before she left for work.
That Saturday afternoon, on May 28, the New Zealander was found dead at a tanning salon in Swansea, Wales.
Piata Tauwhare was healthy, loved to exercise, ate well, didn't smoke and rarely drank alcohol, Jones told the Herald on Sunday.
While her death is being investigated by the Coroner, Jones had been told by police the cause was suspected to be sudden arrhythmic death syndrome (SADS), also known as sudden adult death syndrome..
SADS is an umbrella term used to describe deaths of otherwise healthy people, usually under 40, after their heart stops beating, due to an, often undiagnosed, genetic instability of the heart.
The condition is different from a heart attack which occurs when an artery that sends blood and oxygen to the heart is blocked due to fatty, cholesterol-containing deposits that is built up over time.Hokitika-born Tauwhare had no known heart condition and no family history of heart disease, Jones said.
Knowing nothing about SADS has meant Jones has been left with more questions than answers and, he says, his world has been shattered.
"It destroyed my life. I go to football practice and I come home and she's not there, my life is ruined," he told the Herald on Sunday.
"She was everything to me, so down-to-earth, never had a bad thing to say about anybody."
New Zealand's Coroner's office has recorded 16 deaths caused by SADS in the last five years but the total number of Kiwis who have died from the genetic condition is likely to be much higher as not all deaths are referred to the Coroner.
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A registry was developed in 2008 by cardiologist and electrophysiologist Martin Stiles and a team at the University of Auckland's Waikato Clinical School, thanks to seed funding from Cure Kids.
It aims to help detect and protect young people who may be at risk of SADS.
Anyone who has died from or survived a cardiac arrest with no known cause can be referred to Stiles and his team by hospitals, often cardiologists. The Ministry of Justice may also refer deaths without a cause.
Further testing is then carried out to confirm SADS. Then, researchers work to track down family members who may be at risk and if they would like to get a genetic blood test.
Stiles said for most conditions there was a 50 per cent risk for each first-degree relative.
"We are most interested in it affecting young people so that's generally people between the age of one and 40, after which time non-genetic diseases start to dominate," Stiles said.
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Stiles said they have 5092 registered - mostly at-risk family members, along with some who had died of SADS.
"When the family sees us about their loved one who has died, they are grieving and oddly enough sometimes they have some guilt about the fact that they have passed on a hereditary disease to their child. Yet they are no more guilty of passing on a genetic disease than they are for passing on a gene for blue eyes."
He said his team, which included social workers, psychologists and genetic counsellors worked to help families through this process of investigating why their child died.
There are a number of preventions that could help lower the risk, Stiles said including avoiding certain activities and reducing alcohol intake.
Getting a fever can be a high-risk period, so those at risk need to "be aggressive" about treating that fever with paracetamol and fluids.
People at risk of SADS may need a defibrillator implanted to shock their heart if they have a cardiac arrest.
While Auckland, Waikato and Wellington each have someone working to track down families across their wider regions, Stiles said, there was nobody available in the South Island.
"It's a bit weird that's the way it's happened but that's just the way the funding has fallen."
The team had applied for further research funding with Pūtahi Manawa, Healthy Hearts for Aotearoa New Zealand (HHANZ), to fill this inequity gap.
They were due to hear back about whether that had been successful in the coming weeks, Stiles said.
There were also ethnic disadvantages as there were far fewer people with Polynesian ancestry known to have the genetic condition compared to those with European ancestry. This meant it was harder to test Māori and Pasifika as their genetic database - made up of known mutations - wasn't as big as their Pākehā counterparts.
Stiles said further funding would help to address this.
"We will look at Māori families affected by inherited disease who don't have a genetic diagnosis and we will do detailed genetic studies with the aim of 'upgrading' any genetic variants to 'disease-causing mutations'."
A South Island registry for SADS would help families like that of Greg Watchman, 57, who died after returning from an hour-long bike ride.
On a gusty November afternoon, the Blenheim father used a ladder to get an umbrella that had blown onto the roof.
When he came back down he was short of breath. He asked his 17-year-old step-daughter to fetch him a paper bag to breathe into.
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She did but by the time she returned, he had collapsed onto the ground.
"Her boyfriend performed CPR straight away and I was home within six or seven minutes. By that time the ambulance and fire brigade were there," Greg's wife Andrea said.
CPR was carried out for 40 minutes but he could not be revived. He died on November 15, 2018.
That day still haunts Andrea.
"It was completely out of the blue and no one saw it coming. I still don't really understand what happened," his widow said.
Meanwhile, Jones, a warehouse worker, said losing his wife had been incredibly tough for him, friends and family.
"I'm a mess, I'm just depressed and I don't know what to do with myself."
He said Tauwhare's family and friends had shown him much love and support when he visited New Zealand a few months ago.
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Her family were understandably devastated, Jones said.
The couple had met on a night out in Bristol, England two years ago, while the Kiwi was travelling.
"She was amazing, I've never [met] anyone like that before," Jones said.
The pair married on September 1 last year, in a small ceremony in Swansea, witnessed only by his parents.
Jones described his wife - who was working for a mental health wellbeing service called VitaMinds - as a very generous person and extremely proud of her Kiwi roots.
Other Kiwis lost to SADS
Anita Dell, a mum of two from Blenheim, was 38 when her husband woke to her gasping. She went into cardiac arrest and could not be revived. She had no prior heart condition or underlying health condition.
Leanne Gardyne, a mum of three from Richmond, was 46 when her husband awoke to her struggling to breathe in August 2019. Her hands were clenched, she was shaking, and her pupils were dilated. He moved her to the floor to assist her breathing and then called emergency services, but she was unable to be revived. She had worked as a seafood process worker.
Charles Gray, 66, from Blenheim, was reported to be in "good spirits" the day he died. He had been cooking eggs when they began burning and the house filled with smoke. He was found dead on the lawn a short time after.
Nikki Goodfellow, a 50-year-old checkout operator from Mapua, was loudly gasping for air in her sleep. Her husband tried to wake her but failed. The fire crew were first to the scene and could not revive her.
Gerald Scott, 70, from Nelson was found by a passing motorist unresponsive on a public footpath in Nelson. Emergency services performed CPR but he was unable to be revived.
Phillip Patira, 52, from Christchurch was playing golf when he was seen to become short of breath, clutch his chest, collapse and become unresponsive. He had suffered non-insulin-dependent diabetes, hypertension, gout, and increased BMI. The cause of death was SADS, the Coroner found.
Monday, 9 May 2022
Unpacking Geert vanden Bossche's 'FINAL CALL’
This is my best effort of conveying what Geert vanden Bossche had to say. By necessity, like vanden Bossche himself when he talks there will be some repetition.
Last Friday Del Bigtree of the Highwire interviewed Belgian vaccinologist, Geert vanden Bossche for the third time with not only an update but what he calls his final warning.
His arguments are very technical and difficult to grasp - more so than last time when he did not use such a plethora of confusing concepts to explain what he is seeing.
We have spent much of two days trying to grasp what he is saying and to put it in a language that will be comprehensible to those with a basic, but not extensive understanding of virology or evolutionary biology.
What follows is our attempt to bring clarity to a complicated subject.
What I will do is to reproduce what Geert vanden Bossche has to say as best as I can and to provide an initial attempt to unpack that.
To help this I put together a 50 minute video that brings together all the main parts of his presentation.
First, I have to make my own position clear.
Geert is a vaccinologist and evolutionary biologist and so brings his own understanding.
It is my belief that this should be viewed on its own merit and not compared, positively or negatively, with other conclusions that one has taken on.
That would be what I call "contempt prior to investigation".
I am a great enemy of reductionism and the argument that this ipso facto cannot be true because it "contradicts" something else we have taken on. For example, Geert does not talk as others do, such as Peter McCullough or Robert Malone about the nature of the mRNA shot that is not at all a vaccine.
The evidence to me points to the vaccine being an instrument of genocide because of the many mechanisms of injury in the shot (40 of which have been identified from scientific papers by Dr. Sherri Tenpenny).
However, this does not, in any way, to me contradict the contribution of vanden Bossche. It is bringing a different understanding that reinforces the arguments for keeping well away from the "vaccine", especially when it comes to our children.
For what it is worth Dr. Tenpenny on Telegram advised people to watch the video and to keep watching it until they understand it.
It matters little to me that vanden Bossche is an "insider" who has in the past worked for GAVI, or treats the mRNA shot as a "vaccine" and fails to point out things that are actually well outside his scope of practise.
It is, in my mind, essential that people have a grasp of the dire danger so that they understand just how important it is to avoid the shot for us and our children.
I have always regarded it as far more important to remain aware of the greatest dangers rather than live as if the times are normal.
The "information" that comes from the authorities is deceptively simple (nay, simplistic)- and very easy to grasp but highly misleading.
What Geert vanden Bossche is talking about is immune escape that has been defined as:
"Immune escape (aka viral escape and antigen escape) is the ability of a virus to elude an individual’s immune response."
To summarise, what Geert has been talking about since early 2021 is the danger and folly of vaccinating people in the midst of a pandemic.
As opposed to innate immunity in the population, the vaccines produce non-sterilising (or non-neutralising) antibodies which puts immune pressure on the virus encouraging it to mutate rapidly. This was expressed very clearly by Del Bigtree last year using the analogy of killing killer whales and not sharks.
Here are some of what we gleaned from the interview.
THE PANDEMIC IS FAR FROM OVER
The assumption on the part of Fauci and the propagandists for the vaccine is that the pandemic is all but over .
However, the extent of infection is wildly underestimated.
A lot of people are being infected and reinfected and we are seeing one wave after the other.
Infectious pressure is greater than ever before and the virus has become largely immune to potentially sterilising antibodies.
We are being told the vaccines are preventing serious disease but Geert vanden Bossche says:
"Have you heard of a vaccine that increases susceptibility to disease, protects against serious disease but not against mild disease?"

Omicron is not causing serious disease but mild disease.
It does not produce neutralising antibodies but instead induces the production of non neutralising antibodies.
In a normal pandemic prior to mass vaccination we could expect a limited number of waves of infection and you get back to baseline and the morbidity rates closely would follow the case rates.
This can be seen in the case of South Africa where rates of vaccination are low at around 35%.

But in Omicron never goes back to baseline and we have shorter gaps.

Vanden Bossche states that the vaccinologists and public health authorities overlook that the aim in Nature is to establish an equilibrium between the virus and the host.
You can only do that by controlling the spread and you can only do that if you have neutralising antibodies.
Public health authorities make the sole criterion the number of hospitalisations to persuade us the pandemic is over.
I have been grappling with the situation where in New Zealand where there were 27 deaths "FROM covid" and we were all locked down but now cases, deaths, hospitalisations are way up we are debating the relaxation of restrictions and whether the pandemic is "over".
Just today we had instant confirmation with the announcement of two new variants in New Zealand.
BA.5 arrives: Aotearoa's Covid-19 case numbers will rise - expert
Epidemiologist Michael Baker is predicting New Zealand's Covid-19 case numbers will rise again over the coming months - resulting in increased hospitalisations and deaths.

All that in spite of findings such as the following:

None of that ever made any sense but Geert has explained it to me.
Instead, they continue to propagate the following:



All of that is nonsense of course. Now you can see the likes of Fauci backtracking and flip flopping without ever admitting that he was even a tiny bit wrong.
Sociopaths don't do that.
IMMUNE PRESSURE
With omicron people are getting reinfected because it is the antibodies that are determining - the virus is now free; it no longer has a problem with transmission.
It is now highly transmissive.
The virus is no longer trying to decide how to be more infectious.
The virus is working out how to get round non neutralising antibodies, so it will now will be virulent as well.
For now the omicron variant is, at the moment, preventing transinfection in lungs. It is selecting for a way to get round.
Once that happens transfection will happen in lungs and people will get severe disease in the lungs.
We were putting pressure on the receptor domain protein, the ACE 2 receptor to stop it getting into the cells.
Every time person gets reinfected these non neutralising antibodies are going to be boosted.
The idea that is put forward by Fauci and people like Paul Offit is that the virus will burn itself out and if the vaccine becomes ineffective second generation vaccines can be developed to deal with new variants.
They are, in the opinion of vanden Bossche, using the vaccine as if we were operating outside a pandemic and vaccinating in a normal, prophylactic way.
It is very very clear that the virus will mutate.
It cannot afford to just become virulent. It has to maintain its high level of infectiousness to survive
It cannot afford to just become virulent. It has to maintain its high level of infectiousness to survive
THE IMPORTANCE OF GLYCANS

Vanden Bossche says that a key role is played by glycans.
40% of the surface of the virus is covered in sugars called glycans that are synthesised by the machinery of the host.
They are not recognised by the immune system.
One sugar can SHIELD the entire immune epitopes that are present in the receptor binding domain.
One mutation is all that is needed to reach this situation.
If it doesn't do anything it will get eradicated because - the best way for the virus to propagate is if the host gets mild or moderate disease.
The virus is under extreme immune pressure and so it will mutate.
It cannot afford to just become virulent; it has to maintain its high level of infectiousness, so it needs to combine 2 things - enhanced binding of the non neutralising antibodies to ensure enhanced infectiousness at the upper respiratory tract and preventing , through the antibodies transinfection at the level of the lower respiratory tract.
Glycans need to come in to help the virus meet both these challenges because the responsible antibodies are the same, the non neutralising antibodies need to to ensure enhanced infectiousness whereas they have to prevent them from binding to the virus that is absorbed from the migrating dendritic cells migrating from the upper respiratory tract in order to enable virulence.

The virus is not going to try and eliminate the non-neutralising antibodies because it needs them
It needs them to be infectious.
It is therefore not going to mutate in the way the experts say ( to die out)
It uses the sugar to hide itself so then the blocking of transinfection can happen. The dendritic cells become a vehicle, a taxi cab to bring the virus into the lower respiratory tract.

This mutation got around the neutralising antibodies so the receptor binding domain is freed up and the way the neutralising antibodies are grabbing on is happening faster and enhancing the disease
However, those same antibodies that are enhancing the disease are doing two different jobs.
Those same antibodies that are enhancing the disease are stopping the virus from transinfecting cells in the lower respiratory tract.
It needs the non-neutralising antibodies to be infectious.

It’s not going to get rid of them.
It wants to use them to get through the doors and find a way to continue trans infection which is currently being blocked.
It’s going to use a sugar to coat itself, to hide itself, so that then blocking of transinfection can happen.
Hiding those antibodies that are using it to stop infection by hiding it in sugar can, give rise to serious problems.
A MASSIVE DISASTER WAITING TO HAPPEN
If we wait and see and continue vaccinating it will become too late to do anything, a scenario vanden Bossche hints at.
The more the glycans grow the better they can do their job.
"There will not be one super-variant but rather a series of variants that have greater levels of glycogenation that will overcome the immune pressure that we are putting on the virus that will lead to a rapid succession of variants that have a level of infectiousness that is even higher than omicron so this will not be prevented by the glycans because they will not cover the receptor binding domain that is responsible for increased infectiousness."
SAID IN LAY PERSON'S TERMS
We put this together to try and translate what we heard into language we better understand. No doubt it can do with some improvement

"The virus now has an enormous choice of all possible mutants and plenty of opportunities for infection. Two glycochelation sites on the terminus of the receptor binding domain are already available, but the glycans (sugars) are only present now in trace amounts. With the increase in sugars we will have a series of variants with increasing amounts of glycochelation that will see a level of infectiousness even higher than Omicron."
Geert thinks it may be only a month or two before we start to see highly infectious variants with more extensive glyco-chelation that will render the virus completely resistant.
"The experiment we are doing now is exactly what I would do. Immunising all the children. It’s criminal. It’s not going to have a happy ending, unless we do a dramatic reduction of the infectious pressure."
"This theory is one piece of the puzzle. You cannot leave any stone unturned. You come up with a theory. You need to see how it is being matched in reality. I am investing in doing the research, looking at the science. My frustration is that the message is so difficult to convey, whereas this naive narrative that these people are spreading is so easy - shut up, and get yourself vaccinated - and get your kids vaccinated.
"This will be the biggest disaster ever because this is the biggest reservoir for herd immunity. The more children we vaccinate the more we will expedite this immune escape and get to a kind of variant that will be fully immune to the vaccines and highly virulent. "
THE UNVACCINATED AND THE CHILDREN
In the unvaccinated the innate immune system does not distinguish and recognise cell glycan atoms on pathogens fir example.
A change in the glycogenation is not going to prevent them from recognising them.
For the unvaccinated omicron is like a light-weighted vaccine

When Geert started he understood 60-70% of what is happening.
He now understands the virus is even more sophisticated and working in two stages.
There is no way, in the context of the ongoing vaccination that we can prevent this scenario unless we carry out a massive campaign of prophylaxis using hydroxychloriquine, ivermectin or antivirals like Pavloxid to diminish the infectious pressure.
Prophylaxis would have to be repeated monthly or six-monthly for as long as the small part of the population that is capable of generating genuine herd immunity starts to grow again
As an aside, Igor Chudov in his Substack says Pavloxid does not work in the vaccinated.
Things could go very fast and we may be only a couple of mutations away from this scenario and he surmised this could happen in a matter of a couple of months.
If you leave nature to do itself it will eventually restore balance but Geert asks, "do you want to do this?"
If you let nature do the job and restore homeostasis then large numbers of people are going to die
He does not think this is going to happen because it will take a massive campaign and will take Fauci and others to admit they were completely wrong.
He does not know the numbers but what he can say is the losses will be unprecedented.
This experiment is completely unprecedented and is massive, involving all populations and age groups so the damage will also be massive
When the first information came out we should never have had vaccine mandates; we should have had debate mandates
A complicated matter that has been shaped through millions of years through evolution and these people can destroy everything in an instant like the Taliban or ISIS destroying antiquity with one bomb blast. He has this vision as he contemplates the stupidity, arrogance and obstinance of humanity.
The message is to stay away from the vaccine and to leave our children alone
The unvaccinated are the future of the world.
The countries such as in Africa that barely vaccinate will be the winners.
He gives the example of South Africa (35% vaccinated): where there is a steep increase of one omicron variant, then it is calm for a few months and then you have another steep curve.
You don’t see this any more in highly-vaccinated countries.
The children are the biggest route to herd immunity because they have innate immunity to clear this virus.
The more we vaccinate children the more we will expedite this immune escape.
"There will not be one super-variant but rather a series of variants that have greater levels of glycogenation that will overcome the immune pressure that we are putting on the virus that will lead to a rapid succession of variants that have a level of infectiousness that is even higher than omicron so this will not be prevented by the glycans because they will not cover the receptor binding domain that is responsible for increased infectiousness".
When the first information came out we should never have had vaccine mandates; we should have had debate mandates
GEERT CENSORED
Other key scientists such as Robert Malone, Peter McCullough and others have been widely censored and cancelled - the authorities are determined that their message not be heard. It is a little different with Geert - it is still not hard to find his interviews on the internet and he has no been villified but he seems to be invisible.
For example,when I entered the exact title of the following paper of his nothing came up on the search engines

Most of the criticism comes from "covid-sceptics" who are totally unwilling to grapple with the ideas. For example, Rosemary Frei who I have never head of outside of her attacks on him. For example:
The Vanden Bossche Caper Continues
I exposed Geert Vanden Bossche’s disinformation campaign in a March 16, 2021, article. Unfortunately, he continues to fear-monger, with the active support of high-profile leaders in the Covid-sceptic community
When people talk straight-of-the bat about "disinformation" and "fear-mongering" I switch off immediately.
They are not even worthy of consideration.
I come back to the start of the article and will assert that his contribution is invaluable, an important part of the picture and besides, what he has asserted in the last 14 months has largely come to pass even if explanations may vary.
Now that you have seen my explanations you should now watch the entire program
First, I have to make my own position clear.
Geert is a vaccinologist and evolutionary biologist and so brings his own understanding.
It is my belief that this should be viewed on its own merit and not compared, positively or negatively, with other conclusions that one has taken on.
That would be what I call "contempt prior to investigation".
I am a great enemy of reductionism and the argument that this ipso facto cannot be true because it "contradicts" something else we have taken on. For example, Geert does not talk as others do, such as Peter McCullough or Robert Malone about the nature of the mRNA shot that is not at all a vaccine.
The evidence to me points to the vaccine being an instrument of genocide because of the many mechanisms of injury in the shot (40 of which have been identified from scientific papers by Dr. Sherri Tenpenny).
However, this does not, in any way, to me contradict the contribution of vanden Bossche. It is bringing a different understanding that reinforces the arguments for keeping well away from the "vaccine", especially when it comes to our children.
For what it is worth Dr. Tenpenny on Telegram advised people to watch the video and to keep watching it until they understand it.
It matters little to me that vanden Bossche is an "insider" who has in the past worked for GAVI, or treats the mRNA shot as a "vaccine" and fails to point out things that are actually well outside his scope of practise.
It is, in my mind, essential that people have a grasp of the dire danger so that they understand just how important it is to avoid the shot for us and our children.
I have always regarded it as far more important to remain aware of the greatest dangers rather than live as if the times are normal.
The "information" that comes from the authorities is deceptively simple (nay, simplistic)- and very easy to grasp but highly misleading.
What Geert vanden Bossche is talking about is immune escape that has been defined as:
"Immune escape (aka viral escape and antigen escape) is the ability of a virus to elude an individual’s immune response."
To summarise, what Geert has been talking about since early 2021 is the danger and folly of vaccinating people in the midst of a pandemic.
As opposed to innate immunity in the population, the vaccines produce non-sterilising (or non-neutralising) antibodies which puts immune pressure on the virus encouraging it to mutate rapidly. This was expressed very clearly by Del Bigtree last year using the analogy of killing killer whales and not sharks.
Here are some of what we gleaned from the interview.
THE PANDEMIC IS FAR FROM OVER
The assumption on the part of Fauci and the propagandists for the vaccine is that the pandemic is all but over .
However, the extent of infection is wildly underestimated.
A lot of people are being infected and reinfected and we are seeing one wave after the other.
Infectious pressure is greater than ever before and the virus has become largely immune to potentially sterilising antibodies.
We are being told the vaccines are preventing serious disease but Geert vanden Bossche says:
"Have you heard of a vaccine that increases susceptibility to disease, protects against serious disease but not against mild disease?"

Omicron is not causing serious disease but mild disease.
It does not produce neutralising antibodies but instead induces the production of non neutralising antibodies.
In a normal pandemic prior to mass vaccination we could expect a limited number of waves of infection and you get back to baseline and the morbidity rates closely would follow the case rates.
This can be seen in the case of South Africa where rates of vaccination are low at around 35%.

But in Omicron never goes back to baseline and we have shorter gaps.

Vanden Bossche states that the vaccinologists and public health authorities overlook that the aim in Nature is to establish an equilibrium between the virus and the host.
You can only do that by controlling the spread and you can only do that if you have neutralising antibodies.
Public health authorities make the sole criterion the number of hospitalisations to persuade us the pandemic is over.
I have been grappling with the situation where in New Zealand where there were 27 deaths "FROM covid" and we were all locked down but now cases, deaths, hospitalisations are way up we are debating the relaxation of restrictions and whether the pandemic is "over".
Just today we had instant confirmation with the announcement of two new variants in New Zealand.
BA.5 arrives: Aotearoa's Covid-19 case numbers will rise - expert
Epidemiologist Michael Baker is predicting New Zealand's Covid-19 case numbers will rise again over the coming months - resulting in increased hospitalisations and deaths.

All that in spite of findings such as the following:

None of that ever made any sense but Geert has explained it to me.
Instead, they continue to propagate the following:



All of that is nonsense of course. Now you can see the likes of Fauci backtracking and flip flopping without ever admitting that he was even a tiny bit wrong.
Sociopaths don't do that.
IMMUNE PRESSURE
With omicron people are getting reinfected because it is the antibodies that are determining - the virus is now free; it no longer has a problem with transmission.
It is now highly transmissive.
The virus is no longer trying to decide how to be more infectious.
The virus is working out how to get round non neutralising antibodies, so it will now will be virulent as well.
For now the omicron variant is, at the moment, preventing transinfection in lungs. It is selecting for a way to get round.
Once that happens transfection will happen in lungs and people will get severe disease in the lungs.
We were putting pressure on the receptor domain protein, the ACE 2 receptor to stop it getting into the cells.
Every time person gets reinfected these non neutralising antibodies are going to be boosted.
The idea that is put forward by Fauci and people like Paul Offit is that the virus will burn itself out and if the vaccine becomes ineffective second generation vaccines can be developed to deal with new variants.
They are, in the opinion of vanden Bossche, using the vaccine as if we were operating outside a pandemic and vaccinating in a normal, prophylactic way.
It is very very clear that the virus will mutate.
It cannot afford to just become virulent. It has to maintain its high level of infectiousness to survive
It cannot afford to just become virulent. It has to maintain its high level of infectiousness to survive
THE IMPORTANCE OF GLYCANS

Vanden Bossche says that a key role is played by glycans.
40% of the surface of the virus is covered in sugars called glycans that are synthesised by the machinery of the host.
They are not recognised by the immune system.
One sugar can SHIELD the entire immune epitopes that are present in the receptor binding domain.
One mutation is all that is needed to reach this situation.
If it doesn't do anything it will get eradicated because - the best way for the virus to propagate is if the host gets mild or moderate disease.
The virus is under extreme immune pressure and so it will mutate.
It cannot afford to just become virulent; it has to maintain its high level of infectiousness, so it needs to combine 2 things - enhanced binding of the non neutralising antibodies to ensure enhanced infectiousness at the upper respiratory tract and preventing , through the antibodies transinfection at the level of the lower respiratory tract.
Glycans need to come in to help the virus meet both these challenges because the responsible antibodies are the same, the non neutralising antibodies need to to ensure enhanced infectiousness whereas they have to prevent them from binding to the virus that is absorbed from the migrating dendritic cells migrating from the upper respiratory tract in order to enable virulence.

The virus is not going to try and eliminate the non-neutralising antibodies because it needs them
It needs them to be infectious.
It is therefore not going to mutate in the way the experts say ( to die out)
It uses the sugar to hide itself so then the blocking of transinfection can happen. The dendritic cells become a vehicle, a taxi cab to bring the virus into the lower respiratory tract.

This mutation got around the neutralising antibodies so the receptor binding domain is freed up and the way the neutralising antibodies are grabbing on is happening faster and enhancing the disease
However, those same antibodies that are enhancing the disease are doing two different jobs.
Those same antibodies that are enhancing the disease are stopping the virus from transinfecting cells in the lower respiratory tract.
It needs the non-neutralising antibodies to be infectious.

It’s not going to get rid of them.
It wants to use them to get through the doors and find a way to continue trans infection which is currently being blocked.
It’s going to use a sugar to coat itself, to hide itself, so that then blocking of transinfection can happen.
Hiding those antibodies that are using it to stop infection by hiding it in sugar can, give rise to serious problems.
A MASSIVE DISASTER WAITING TO HAPPEN
If we wait and see and continue vaccinating it will become too late to do anything, a scenario vanden Bossche hints at.
The more the glycans grow the better they can do their job.
"There will not be one super-variant but rather a series of variants that have greater levels of glycogenation that will overcome the immune pressure that we are putting on the virus that will lead to a rapid succession of variants that have a level of infectiousness that is even higher than omicron so this will not be prevented by the glycans because they will not cover the receptor binding domain that is responsible for increased infectiousness."
SAID IN LAY PERSON'S TERMS
We put this together to try and translate what we heard into language we better understand. No doubt it can do with some improvement

"The virus now has an enormous choice of all possible mutants and plenty of opportunities for infection. Two glycochelation sites on the terminus of the receptor binding domain are already available, but the glycans (sugars) are only present now in trace amounts. With the increase in sugars we will have a series of variants with increasing amounts of glycochelation that will see a level of infectiousness even higher than Omicron."
Geert thinks it may be only a month or two before we start to see highly infectious variants with more extensive glyco-chelation that will render the virus completely resistant.
"The experiment we are doing now is exactly what I would do. Immunising all the children. It’s criminal. It’s not going to have a happy ending, unless we do a dramatic reduction of the infectious pressure."
"This theory is one piece of the puzzle. You cannot leave any stone unturned. You come up with a theory. You need to see how it is being matched in reality. I am investing in doing the research, looking at the science. My frustration is that the message is so difficult to convey, whereas this naive narrative that these people are spreading is so easy - shut up, and get yourself vaccinated - and get your kids vaccinated.
"This will be the biggest disaster ever because this is the biggest reservoir for herd immunity. The more children we vaccinate the more we will expedite this immune escape and get to a kind of variant that will be fully immune to the vaccines and highly virulent. "
THE UNVACCINATED AND THE CHILDREN
In the unvaccinated the innate immune system does not distinguish and recognise cell glycan atoms on pathogens fir example.
A change in the glycogenation is not going to prevent them from recognising them.
For the unvaccinated omicron is like a light-weighted vaccine

When Geert started he understood 60-70% of what is happening.
He now understands the virus is even more sophisticated and working in two stages.
There is no way, in the context of the ongoing vaccination that we can prevent this scenario unless we carry out a massive campaign of prophylaxis using hydroxychloriquine, ivermectin or antivirals like Pavloxid to diminish the infectious pressure.
Prophylaxis would have to be repeated monthly or six-monthly for as long as the small part of the population that is capable of generating genuine herd immunity starts to grow again
As an aside, Igor Chudov in his Substack says Pavloxid does not work in the vaccinated.
Things could go very fast and we may be only a couple of mutations away from this scenario and he surmised this could happen in a matter of a couple of months.
If you leave nature to do itself it will eventually restore balance but Geert asks, "do you want to do this?"
If you let nature do the job and restore homeostasis then large numbers of people are going to die
He does not think this is going to happen because it will take a massive campaign and will take Fauci and others to admit they were completely wrong.
He does not know the numbers but what he can say is the losses will be unprecedented.
This experiment is completely unprecedented and is massive, involving all populations and age groups so the damage will also be massive
When the first information came out we should never have had vaccine mandates; we should have had debate mandates
A complicated matter that has been shaped through millions of years through evolution and these people can destroy everything in an instant like the Taliban or ISIS destroying antiquity with one bomb blast. He has this vision as he contemplates the stupidity, arrogance and obstinance of humanity.
The message is to stay away from the vaccine and to leave our children alone
The unvaccinated are the future of the world.
The countries such as in Africa that barely vaccinate will be the winners.
He gives the example of South Africa (35% vaccinated): where there is a steep increase of one omicron variant, then it is calm for a few months and then you have another steep curve.
You don’t see this any more in highly-vaccinated countries.
The children are the biggest route to herd immunity because they have innate immunity to clear this virus.
The more we vaccinate children the more we will expedite this immune escape.
"There will not be one super-variant but rather a series of variants that have greater levels of glycogenation that will overcome the immune pressure that we are putting on the virus that will lead to a rapid succession of variants that have a level of infectiousness that is even higher than omicron so this will not be prevented by the glycans because they will not cover the receptor binding domain that is responsible for increased infectiousness".
When the first information came out we should never have had vaccine mandates; we should have had debate mandates
GEERT CENSORED
Other key scientists such as Robert Malone, Peter McCullough and others have been widely censored and cancelled - the authorities are determined that their message not be heard. It is a little different with Geert - it is still not hard to find his interviews on the internet and he has no been villified but he seems to be invisible.
For example,when I entered the exact title of the following paper of his nothing came up on the search engines

Most of the criticism comes from "covid-sceptics" who are totally unwilling to grapple with the ideas. For example, Rosemary Frei who I have never head of outside of her attacks on him. For example:
The Vanden Bossche Caper Continues
I exposed Geert Vanden Bossche’s disinformation campaign in a March 16, 2021, article. Unfortunately, he continues to fear-monger, with the active support of high-profile leaders in the Covid-sceptic community
When people talk straight-of-the bat about "disinformation" and "fear-mongering" I switch off immediately.
They are not even worthy of consideration.
I come back to the start of the article and will assert that his contribution is invaluable, an important part of the picture and besides, what he has asserted in the last 14 months has largely come to pass even if explanations may vary.
Now that you have seen my explanations you should now watch the entire program






