At the outset, Dr. Yeadon said “I’m well aware of the global crimes against humanity being perpetrated against a large proportion of the worlds population.
The post below is from America’s Frontline Doctors, the ONLY doctors plus a few others that you can trust regarding information about this COVID-19 mess. Dr Anthony FauXci is NOT one of those doctors.
Is Covid-19 Vaccine Used For Massive-Scale Depopulation Weapon?? Keep reading.
This video is from the David Knight show and is separate from this post, but the information is totally relevant.
Exclusive: Former Pfizer VP to AFLDS: ‘Entirely possible this will be used for massive-scale depopulation’
March 25, 2021 | Comments Off on Exclusive: Former Pfizer VP to AFLDS: ‘Entirely possible this will be used for massive-scale depopulation’
by Mordechai Sones
America’s Frontline Doctors (AFLDS) spoke to former Pfizer Vice President and Chief Science Officer Dr. Mike Yeadon about his views on the COVID-19 vaccine, hydroxychloroquine and ivermectin, the regulatory authorities, and more.
At the outset, Dr. Yeadon said “I’m well aware of the global crimes against humanity being perpetrated against a large proportion of the worlds population.
“I feel great fear, but I’m not deterred from giving expert testimony to multiple groups of able lawyers like Rocco Galati in Canada and Reiner Fuellmich in Germany.
“I have absolutely no doubt that we are in the presence of evil (not a determination I’ve ever made before in a 40-year research career) and dangerous products.
“In the U.K., it’s abundantly clear that the authorities are bent on a course which will result in administering ‘vaccines’ to as many of the population as they can. This is madness, because even if these agents were legitimate, protection is needed only by those at notably elevated risk of death from the virus. In those people, there might even be an argument that the risks are worth bearing. And there definitely are risks which are what I call ‘mechanistic’: inbuilt in the way they work.
“But all the other people, those in good health and younger than 60 years, perhaps a little older, they don’t perish from the virus. In this large group, it’s wholly unethical to administer something novel and for which the potential for unwanted effects after a few months is completely uncharacterized.
“In no other era would it be wise to do what is stated as the intention.
“Since I know this with certainty, and I know those driving it know this too, we have to enquire: What is their motive?
“While I don’t know, I have strong theoretical answers, only one of which relates to money and that motive doesn’t work, because the same quantum can be arrived at by doubling the unit cost and giving the agent to half as many people. Dilemma solved. So it’s something else. Appreciating that, by entire population, it is also intended that minor children and eventually babies are to be included in the net, and that’s what I interpret to be an evil act.
“There is no medical rationale for it. Knowing as I do that the design of these ‘vaccines’ results, in the expression in the bodies of recipients, expression of the spike protein, which has adverse biological effects of its own which, in some people, are harmful (initiating blood coagulation and activating the immune ‘complement system’), I’m determined to point out that those not at risk from this virus should not be exposed to the risk of unwanted effects from these agents.”
AFLDS: The Israel Supreme Court decision last week cancelling COVID flight restrictions said: “In the future, any new restrictions on travel into or out of Israel need, in legal terms, a comprehensive, factual, data-based foundation.”
“The most likely duration of immunity to a respiratory virus like SARS CoV-2 is multiple years. Why do I say that? We actually have the data for a virus that swept through parts of the world seventeen years ago called SARS, and remember SARS CoV-2 is 80% similar to SARS, so I think that’s the best comparison that anyone can provide.
“The evidence is clear: These very clever cellular immunologists studied all the people they could get hold of who had survived SARS 17 years ago. They took a blood sample, and they tested whether they responded or not to the original SARS and they all did; they all had perfectly normal, robust T cell memory. They were actually also protected against SARS CoV-2, because they’re so similar; it’s cross immunity.
“So, I would say the best data that exists is that immunity should be robust for at least 17 years. I think it’s entirely possible that it is lifelong. The style of the responses of these people’s T cells were the same as if you’ve been vaccinated and then you come back years later to see if that immunity has been retained. So I think the evidence is really strong that the duration of immunity will be multiple years, and possibly lifelong.”
In other words, previous exposure to SARS – that is, a variant similar to SARS CoV-2 – bestowed SARS CoV-2 immunity.
The Israel government cites new variants to justify lockdowns, flight closures, restrictions, and Green Passport issuance. Given the Supreme Court verdict, do you think it may be possible to preempt future government measures with accurate information about variants, immunity, herd immunity, etc. that could be provided to the lawyers who will be challenging those future measures?
Yeadon: “What I outlined in relation to immunity to SARS is precisely what we’re seeing with SARS-CoV-2. The study is from one of the best labs in their field.
“So, theoretically, people could test their T-cell immunity by measuring the responses of cells in a small sample of their blood. There are such tests, they are not “high throughput” and they are likely to cost a few hundred USD each on scale. But not thousands. The test I’m aware of is not yet commercially available, but research only in U.K.
“However, I expect the company could be induced to provide test kits “for research” on scale, subject to an agreement. If you were to arrange to test a few thousand non vaccinated Israelis, it may be a double edged sword. Based on other countries experiences, 30-50% of people had prior immunity & additionally around 25% have been infected & are now immune.
“Personally, I wouldn’t want to deal with the authorities on their own terms: that you’re suspected as a source of infection until proven otherwise. You shouldn’t need to be proving you’re not a health risk to others. Those without symptoms are never a health threat to others. And in any case, once those who are concerned about the virus are vaccinated, there is just no argument for anyone else needing to be vaccinated.”
My understanding of a “leaky vaccine” is that it only lessens symptoms in the vaccinated, but does not stop transmission; it therefore allows the spread of what then becomes a more deadly virus.
For example, in China they deliberately use leaky Avian Flu vaccines to quickly cull flocks of chicken, because the unvaccinated die within three days. In Marek’s Disease, from which they needed to save all the chickens, the only solution was to vaccinate 100% of the flock, because all unvaccinated were at high risk of death. So how a leaky vax is utilized is intention-driven, that is, it is possible that the intent can be to cause great harm to the unvaccinated.
Stronger strains usually would not propagate through a population because they kill the host too rapidly, but if the vaccinated experience only less-serious disease, then they spread these strains to the unvaccinated who contract serious disease and die.
Do you agree with this assessment? Furthermore, do you agree that if the unvaccinated become the susceptible ones, the only way forward is HCQ prophylaxis for those who haven’t already had COVID-19?
Would the Zelenko Protocol work against these stronger strains if this is the case?
And if many already have the aforementioned previous “17-year SARS immunity”, would that then not protect from any super-variant?
“I think the Geert Vanden Bossche story is highly suspect. There is no evidence at all that vaccination is leading or will lead to ‘dangerous variants’. I am worried that it’s some kind of trick.
“As a general rule, variants form very often, routinely, and tend to become less dangerous & more infectious over time, as it comes into equilibrium with its human host. Variants generally don’t become more dangerous.
“No variant differs from the original sequence by more than 0.3%. In other words, all variants are at least 99.7% identical to the Wuhan sequence.
“It’s a fiction, and an evil one at that, that variants are likely to “escape immunity”.
“Not only is it intrinsically unlikely – because this degree of similarity of variants means zero chance that an immune person (whether from natural infection or from vaccination) will be made ill by a variant – but it’s empirically supported by high-quality research.
“The research I refer to shows that people recovering from infection or who have been vaccinated ALL have a wide range of immune cells which recognize ALL the variants.
“This paper shows WHY the extensive molecular recognition by the immune system makes the tiny changes in variants irrelevant.
“I cannot say strongly enough: The stories around variants and need for top up vaccines are FALSE. I am concerned there is a very malign reason behind all this. It is certainly not backed by the best ways to look at immunity. The claims always lack substance when examined, and utilize various tricks, like manipulating conditions for testing the effectiveness of antibodies. Antibodies are probably rather unimportant in host protection against this virus.
There have been a few ‘natural experiments’, people who unfortunately cannot make antibodies, yet are able quite successfully to repel this virus. They definitely are better off with antibodies than without. I mention these rare patients because they show that antibodies are not essential to host immunity, so some contrived test in a lab of antibodies and engineered variant viruses do NOT justify need for top up vaccines.
“The only people who might remain vulnerable and need prophylaxis or treatment are those who are elderly and/or ill and do not wish to receive a vaccine (as is their right).
“The good news is that there are multiple choices available: hydroxychloroquine, ivermectin, budesonide (inhaled steroid used in asthmatics), and of course oral Vitamin D, zinc, azithromycin etc. These reduce the severity to such an extent that this virus did not need to become a public health crisis.”
Do you feel the FDA does a good job regulating big pharma? In what ways does big pharma get around the regulator? Do you feel they did so for the mRNA injection?
“Until recently, I had high regard for global medicines regulators. When I was in Pfizer, and later CEO of a biotech I founded (Ziarco, later acquired by Novartis), we interacted respectfully with FDA, EMA, and the U.K. MHRA. Always good quality interactions.
“Recently, I noticed that the Bill & Melinda Gates Foundation (BMGF) had made a grant to the Medicines and Healthcare products Regulatory Agency (MHRA)! Can that ever be appropriate? They’re funded by public money. They should never accept money from a private body.
“So here is an example where the U.K. regulator has a conflict of interest.
“The European Medicines Agency failed to require certain things as disclosed in the ‘hack’ of their files while reviewing the Pfizer vaccine.
“You can find examples on Reiner Fuellmich’s “Corona Committee” online.
“Dr. Wolfgang Wodarg and I petitioned the EMA Dec 1, 2020 on the genetic vaccines. They ignored us.
“Recently, we wrote privately to them, warning of blood clots, they ignored us. When we went public with our letter, we were completely censored. Days later, more than ten countries paused use of a vaccine citing blood clots.
“I think the big money of pharma plus cash from BMGF creates the environment where saying no just isn’t an option for the regulator.
“I must return to the issue of ‘top up vaccines’ (booster shots) and it is this whole narrative which I fear will he exploited and used to gain unparalleled power over us.
“PLEASE warn every person not to go near top up vaccines. There is absolutely no need to them.
“As there’s no need for them, yet they’re being made in pharma, and regulators have stood aside (no safety testing), I can only deduce they will be used for nefarious purposes.
“For example, if someone wished to harm or kill a significant proportion of the worlds population over the next few years, the systems being put in place right now will enable it.
In the article republished from Nakim.org, research is presented indicating orders of magnitude increases in death rates during the 5-week long vaccination process analyzed in Israel, as compared to the unvaccinated and those after completing the vaccination process.
Our reanalyses of these data explain why during the massive vaccination project initiated mid-December 2020 during a confinement, daily new confirmed COVID-19 cases failed to decrease as they do during confinements, and, more importantly, why numbers of serious, critical and death cases increased during that period that covered at least one month.
From mid-December to mid-February (two months), 2337 among all Israeli 5351 official COVID-deaths occurred. Our analyses indicate orders of magnitude increases in deaths rates during the 5-week long vaccination process, as compared to the unvaccinated and those after completing the vaccination process. Presumably, asymptomatic cases before vaccination, and those infected shortly after the 1st dose, tend to develop graver symptoms than those unvaccinated.
The Ynet article is organized in an exciting way and uses data provided in an erroneous way by the Ministry of Health. It is unclear whether this was intentional to prove the vaccine’s efficiency or if this was done erroneously because the provided data were misunderstood. Note that in Israel, all vaccines are from Pfizer.
We bring a very important example from the article, in relation to the table provided by the Ministry of Health. As per the text “However, 546 among the dead were such that were not at all vaccinated or got the first vaccination dose within two weeks before their death” differs from the table.
This is clearly unfounded because all data presented in the table and provided below describe only COVID-19 patients that got at least the first vaccination dose. This is clear from examining the table. The grand total is 43781 COVID patients who got the first or the second vaccine dose. Among the total of 660 deaths, 546 got only the first dose.
The Data In The Table, Rather Than Indicating The Vaccine Efficiency, Indicate The Covid-19 Vaccine Adverse Effects
For that purpose we need first to understand that the provided table describes the state of COVID-19 patients that got the first or the second vaccine dose at given dates, as started in the article “…emerges from the data that among 856 patients above 60 years in serious state hospitalized at this time…” we assume that the article published February 11 reflects the situation in hospitals the previous day, hence February 10 2021, or February 11 2021.
Serious Active Cases
On February 10, the number of serious active cases was 1056 according to the control panel of the Ministry of Health, see photo below.
This surprisingly shows that most serious hospitalized cases on February 10 or at a near date were in fact vaccinated with the first dose or up to two weeks after the second dose. See the table of the vaccinated patients showing 1031 serious and 220 critical cases at the time the table was done. This matches the article in hebrew from February 1st 2021 “Can one show that the vaccine from Pfizer is today’s major cause for high death rates in Israel and the world?”.
However, this is not the last surprise we get from examining the data from the Ministry of Health. We can substract the number of people with the first vaccine dose on January 19 2021 from that on February 10 2021. During these 21 days, 1331881 Israeli citizens got the first dose. The table shows that 568 among these died, hence 0.042% and that 39047 among them became a COVID-19 case, hence 2.9 %. For the 2nd dose we focus on data specific to two weeks after the 2nd vaccination according to the table.
From January 26 to February 10 2021 909102 Israeli citizens got the 2nd vaccine dose. Among these according to the table, 92 died, 0.01%. Hence, during the 5 weeks since the first dose at least 0.05% of first dose recipients died. This death rate relates mainly to a relatively young population whose vaccination stated on January 19, a period during which most vaccinated were below 65. In order to estimate the death rate of those above 65 which were mostly vaccinated before that period we use data reported by the USA-based VAERS,
There we found, see article in english, that the ratio of deaths by those above 65 vs those below 65 is about 4.42 (155/35). Hence the death rate of those above 65 between the first and the second vaccination dose should be until January 19 0.042 (the death rate of those below 65) multiplied by 4.42, resulting in 0.186%, which is close to the 0.2% reported by the Ministry of Health on January 21 2021.
This value of 0.2 % death has been mysteriously modified later on by the Ministry of Health and was switched to 0.005 without any explanation, see article in hebrew. Above considerations show that the death rate data provided first were correct, the updated death rate data might have been intended to suggest lower death rates among the elderly.
The exposures do not end here. The number of COVID-19 deaths among the vaccinated since the start of the vaccination action seems to explain the increased death rates from COVID-19 observed since December 2020. For that purpose, we calculate the products of the number of vaccinated people above age 65 by 0.2 and the number of vaccinated people below 65 by 0.04. This shows that most COVID-19 deaths in that period are for vaccinated people, as shows the table provided by the Ministry of health at the beginning of February.
During the vaccination action from mid-December until mid-February, 2337 among all 5351 COVID-19 deaths reported for Israel occurred, 43.7%. Among these, since January 19, 1271 COVID-19 deaths were reported for Israel.The table provided by the Ministry of Health on February 10 states 660 COVID-19 deaths among the vaccinated, 51.9% of the deaths for that period.
Only 1.3 million Israeli, among 8 million (about 1 in 8, 12.5%), were vaccinated during that period. Accordingly, vaccination promotes deaths because 51.9% of deaths during that period are for the 12.5% vaccinated in that period. In addition the serious and critical cases during that period is more than the reported serious cases, the adverse effect of the vaccination process is most likely worse than what appears from the data at hand.
The horror continues. The deaths among those vaccinated should be added to the numerous AVC and cardiac events reported just after vaccination that are not included among COVID-19 deaths which about double the deaths among those vaccinated, whose numbers remain unknown and which we will try to find in the coming days. At this point we state that vaccinations caused more deaths than the coronavirus would have during the same period.
Among those vaccinated and above 65, 0.2% of those vaccinated died during the 3-week period between doses, hence about 200 among 100000 vaccinated. This is to be compared to the 4.91 dead among 100000 dying from COVID-19 without vaccination, see below. This should not be confused with the COVID-19 0.279 deaths among 100000 reported for those who completed the vaccination process, meaning 2 weeks after the second dose, see below table from the Ynet article.
Death Per Age Group
This scary picture also extends to those below 65, among which, for the 5 weeks during the complete vaccination process 0.05%, meaning 50 among 100000, died. This is to be compared to the 0.19 per 100000 dying from COVID-19 and that are not vaccinated in that age group, as per the above table. Hence the death rate of this age group increased by 260 during this 5-week period of the vaccination process, as compared to their natural COVID-19 death rate.
A simple way to pass these points across relate to the monthly COVID-19 deaths rates since the start of the pandemic and until mid-December, 3014 deaths, hence 3014/9 = 334.9 deaths per month. Monthly death rates since mid-December are 2337/2 = 1168.5 deaths per month, hence 3.5 times greater.
We conclude that the Pfizer vaccines, for the elderly, killed during the 5-week vaccination period about 40 times more people than the disease itself would have killed, and about 260 times more people than the disease among the younger age class. We stress that this is in order to produce a green passport valid at most 6 months, and promote Pfizer sales.
These estimated numbers of deaths from the vaccine are probably much lower than actual numbers as it accounts only for those defined as COVID-19 deaths for that short time period and does not include AVC and cardiac (and other) events resulting from the inflammatory reactions in tens of reports documented on the NAKIM site, which themselves are only the iceberg’s tip, see here.
This does not account for long-term complications described in a criminal complaint filed in December 2020 in France and which was translated to english, see here. Looking back, this explains why the serious COVID-19 cases increased as vaccination started, and why cases started to decline when vaccination was opened to the young and continue to decline as the vaccination national campaign is losing its momentum.
We hope that this massacre will not include those below 13, as these have an increased adverse reaction rate, including death, to vaccines as shown by multi-decennial data from the VAERS reports in the USA.
We summarise that the pandemic may be predicted for the coming weeks. The decrease in vaccinations and in vaccination age will cause a decrease in serious cases, mainly not because of the protection by the vaccine, but because fewer people will die from the vaccine and other adverse vaccine reactions.
This will be temporary as in a few months we expect to face mid- and long-term adverse effects of the vaccination as ADE (Antibody-dependent Enhancement) and the vaccination-resistant mutants selected by the vaccines. But this should occur after the soon coming elections and the (survivor) voters won’t have another opportunity to express their disappointment at the voting poll.
Thanks to Dr Hervé Seligmann for his huge support on data analysis.
Also, how does it come that some people are naturally protected and others are not? What are these mechanisms? What are these molecular mechanisms?
Dr Geert Vanden Bossche Interviewed By Dr Philip McMillan Full Interview & Transcript
Dr. Philip McMillan – Hello and good evening to everyone, well, afternoon, depending on where you are in the world today. We have a really, really important topic and I have the pleasure of having with me, Dr. Geert Vanden Bossche from Belgium, the difference is that Geert is truly an international vaccine developer and he’s here to share some very important and unique perspectives on where we are now in terms of the covid pandemic.
Philip: So pleasure to have you here with me Geert. How are you?
Geert: I’m fine thanks for having me, Philip.
Philip: Wonderful, wonderful, listen. I mean, I think the first thing that we have to clarify is that we have to explain, you are someone who is in the vaccine, development business, so to speak. What has that background been like?
Geert: Well, I have a background essentially in as far as vaccines are concerned in industry, as well as in the non-for-profit sector. So I have been working with the Bill & Melinda Gates foundation, GAVI, especially concentrating on vaccines for global health, and I’ve also been working with several different companies – vaccine companies, developing of course, essentially prophylactic vaccines.
My main focus of interest has always been in fact the design of Vaccines so the the concept: how can we educate the immune system in ways that are to some extent more efficient than we do right now, with our conventional vaccines.
Philip: Right and so In effect, this is the area of work you’ve been in you develop vaccines. You are as well working with the Ebola vaccine as well, one of the really really dangerous viruses we have out there in the world. How? How does that work is it? Is that easy to do?
Geert: Well, I was not uh.. let me very clear, I was a coordinator of the Ebola program at GAVI, so we were interacting with several different vaccine companies that were developing Ebola vaccines because it was important for GAVI to make the right choice the right vaccine in order uh, you know for this vaccine to be rolled out in the uh western African uh countries that had this severe Ebola crisis back a number of years ago.
So that was not uh, let’s say operational, practical work, this was more a role of coordination, but, of course, was also a role of assessing what would be the impact of using some of these vaccines in larger populations and in an area where uh an epidemic is is really is, is going on because that’s a very Particular and peculiar situation.
Philip: Yes, and so in fact, we’ve had so much success over the past 100 years with some very big breakthroughs with vaccines, smallpox, you know, measles, mumps, rubella, um, polio, um, but we’ve struggled with other vaccines. It It’s it without going into the details, because this is very difficult to get across, but is there a difference with how viruses operate, that makes some easier to get a vaccine for?
Geert: Well, I think we have Philip, essentially, we need to distinguish, of course, be between what we call acute self-limiting diseases. These are diseases that naturally uh come to an end, in a sense that ultimately, the individual will eliminate the pathogen, of course, some people may die, of course, let’s be very clear.
Those who survive will ultimately eliminate the pathogen that is the vast majority of the vaccines we have been developing so far uh, you know, I Don’t need to tell you that with other viruses, where uh we, we clearly see that they spread in a completely different way. They spread, for example, from cell to cell. They tend to be more intracellular.
They tend to develop chronic infections where It’s uh, It’s not self-limiting, It’s not acute self-limiting, it’s chronic, it is much more difficult, and that is the the reason primarily is that um most of the vaccines we are developing are still antibody based vaccines. So we need these antibodies in the blood or we need these antibodies to translate to the mucosa, for example, in order to capture the pathogen and to neutralize it.
So some of the other bugs I mean they have a very insidious strategy in a sense that they hide in cells that they can already add a mucosal barrier penetrate you know, immediately into cells, and then the cells uh may migrate, for example, to the, to the, the lymph nodes, so they are shielded from the antibodies, and that makes it very, very difficult because we know that we can catch them to some extent in the blood, but what they do all the time is that they insert mutation and they escape they fully escape. To our antibody uh responses, so that makes it uh way more difficult.
It’s also the the model is the reason why also against cancer etc. We have not been extremely successful with vaccines, as I would say, stand-alone uh yeah.
Philip: Absolutely yes! So it brings us into where we are, with regards to covid-19. Now, if we, we have 20 20 vision at the moment when we look back at the pandemic and where we started from, and I’ve always said that at the time when the pandemic started, when it got from China into Italy to Europe into the UK, I thought that the only way that we could manage this is to lock down and to prevent the spread of this apart, this very dangerous virus.
We do have to stand back and see whether or not those decisions were correct, but, as we said that hindsight is 2020. What would you say now, as we look back at the decisions we made then, were we about on the right track? Did we make any mistakes?
Geert: Well, frankly, speaking from the very beginning – and I mean there are many people who can witness this or testify it is, I always said that it was a bad idea to do lock-downs that would also affect the younger people. That we would prevent younger people from having contact from being exposed, because remember the big difference back then was, of course, that we had a viral strain covid strain that was circulating dominant strain, and that was not highly infectious as those that we are seeing right now.
Of course, when a new virus gets into a population, it immediately gets to the folks that, have you know, weak immunity, and we know we know these people, this is to a large majority, of course, elderly people, people uh that have underlying diseases or are otherwise immune, suppressed, etc.
And, of course I mean it was certainly the right thing to do to protect these people and for them also to isolate. But we have to distinguish frankly, and that is what we we have not been doing – between those people that have strong innate immunity, I mean It’s not uh, you cannot see when you see a person, you Don’t know this, but we know that young people have quite decent innate immune response and therefore they are naturally protected and even more I mean if they get in contact with corona virus, it will Boost their natural immunity.
So therefore, from the very beginning – I don’t I was – I disapproved. You know the fact that schools got too close and and universities and that youngsters were preventing even from having contact with each other. That situation is, of course, completely different. If you look at vulnerable people, the viruses comes in the population, there is no no immunity, there is no immunity at all.
In fact, so nobody has been in contact, so the youngsters they can rely on good innate immunity, elderly people I mean the the innate immunity is waning. It gets increasingly replaced by antigen specific by specific immunity as people get older, so these people very, very clearly needed to be protected, but it has taken a lot of time before we understood in fact how we, how exactly the immune response and the virus were interacting.
So there has been a lot of confusion, a lot of mistakes made about mistakes, I mean retrospectively um and, and that has also led to um, you know bad control right from the beginning, uh. I would say…
Philip: So with that in mind and where we are now, as we uh as countries across the world have been drifting towards the Christmas period, there is still a rise in cases, countries had to try and lock down mass mandates and so on, but we all had the hope that vaccines would come and break the cycle. This is where clearly, now from your expertise, you seem to have a different thought about how we should have been thinking about vaccines, then, and even now, what is your perspective?
Geert: Well, my perspective was, and still is, that, if you, if you go to war, you better make sure that you have the right weapon and the weapon in itself can be an excellent weapon, and that is what I’m saying really about the current vaccines. I mean It’s just brilliant people who have been making these vaccines in no time and with regulatory approval and everything.
So the weapon in itself is excellent. Question is: is this the right weapon for the kind of war that is going on right now? And there, my answer is definitely no. Because these are prophylactic vaccines and prophylactic vaccines should typically not be administered to people who are exposed to high infectious pressure.
So Don’t forget, we are administering these vaccines in the heat of a pandemic, so in other words, while we are preparing our weapon, we are fully attacked by the virus, the virus is everywhere. So that is a very different scenario from using such vaccines in, in a setting where the vaccine is barely or not exposed to the virus.
And I’m saying this because if you have high infectious pressure, It’s so easy for the virus to jump from one person to the other. So if your immune response, however, is just mounting, as we see right now with the number of people who get their first dose together, first, those the antibodies are not fully mature, titer are maybe not very high, so their immune response is sub-optimal, but they are in the midst of this war while they are mounting an immune response.
They are fully attacked by by the virus and every single time I mean this is textbook knowledge every single time, you have an immune response that is sub-optimal in the presence of an infection in the presence of a virus that infects that person you are at risk for immune escape.
So that means that the virus can escape to the immune response, and that is why I’m saying that these vaccines – I mean in their own right are, of course, excellent, but to use them in the midst or in the midst of a pandemic and do mass vaccination, because then, you provide within a very short period of time the population with high antibody titers, so the virus comes under enormous pressure.
I mean that that wouldn’t matter, if you can eradicate the fire, if you can prevent infection, but these vaccines don’t prevent infection, they protect against disease. Because we are just, unfortunately, we look no further than the end of our nose in the sense that hospitalization, that’s all what counts.
You know getting people away from the hospital, but in the meantime we are not realizing that we give all the time during this pandemic by our interventions the opportunity who escaped immune to the immune system and and – and that is of course, uh a very, very, very Dangerous thing, especially if we realize that these guys they only need 10 hours to replicate.
So if you think that by making new vaccines a new new vaccine against the the new infectious strains, we are going to catch up, It’s impossible to catch up, I mean virus is not going to wait till we have those vaccines ready. I mean this thing continues and, as I was saying, the thing is I mean if, if you do this in the midst of a pandemic, that is, that is an enormous problem. These vaccines are excellent, but they are not made for administration to millions of people in the midst in the heat of a pandemic. So that is my fault.
Philip: Is this equivalent? Then? Because you mentioned this in your paper, it is equivalent to using either a partial dose of antibiotics in an antimicrobial or in a bacterial infection, where you then produce super-bugs. Is this the kind of example that you’re alluding to well?
Geert: That is a very good parallel. It’s also the parallel I’m using actually in the paper we just posted on Linkedin, which you know should be so open for everybody. I mean It’s pure science, because, as you were pointing out Philip, the thing is the rule is is very simple. I mean same with antibiotics either the antibiotics do not match very well with the bug. That’s not good! That’s why we are making antibiograms.
You know to first identify which, which is this germ, and then we choose the antibiotics. We we need to have a very good match, otherwise there could be resistance. So when I compare this to the current situation, do we have a good match with our antibodies? No, at this point in time we don’t have a good match anymore, because we have this kind of like almost heterologous variants, so that differs from the original strain. So the match isn’t very good anymore and hence we see people are still protected, but they are already shedding the virus.
So that is one thing. The other thing is the quantity. Of course you tell people, you know you take your antibiotics according to the prescription. Please Don’t uh as soon as you feel well that doesn’t mean that that you, you can stop the antibiotics same here, and I give just one example. If you know give people just like one dose, I mean they are in the process of mounting their antibodies.
The antibodies still need to fill the mature, etc. So this is a sub-optimal situation. We are putting them in a sub-optimal situation with regard to their um immune protection and, on the other hand, they are in the midst of the war. They are fully attacked by all you know by all these kinds of highly infectious variants, so I mean It’s It’s very clear that this is driving immune escape and will ultimately drive resistance uh to to the vaccines.
So my point is yes Philip, It’s very similar. There is one difference, the virus needs living cells, I mean if you’re driving immune escape, but the guy has no chance to jump on somebody else who cares? This situation is no different because we are in the midst of a war. We, there is a high infectious pressure, so the likelihood that an immune escape immediately finds another living cell, that means another host is very, very high. It’s per definition It’s the definition almost of a pandemic.
Philip: Yeah, So it raises a simple question that somebody has put in in front of us here, which is It’s perfectly common sense? What do we do?
Geert: That question is very easy. I mean we need, we need to to do a better job when we are confronted with situations that seem very dramatic. Like you know an epidemic, our generation has not, you know, been living in times where there are epidemics or pandemics, and so we immediately take action and and jump on the beast with the tools we have instead of analyzing, what is really going on.
One thing that uh I thought was extremely interesting was and it’s something that was not really understood, we know that the number of people are asymptomatically infected, so they are infected, but they don’t develop severe symptoms.
Of course, they can have some mild symptoms of respiratory disease whatever. So the question is what exactly happens with those folks that they can eliminate the virus? They eliminate the virus, they, they don’t transmit it, they will, they will shed it for like a week or so, and then they eliminate this.
You could say yeah. Of course, we know that antibodies eliminate, oh wait a minute, the antibodies come later. You have first, the search of you know shedding of the virus, and It’s only afterwards that you see you know a moderate and short-lived race of antibodies, so the antibodies cannot be responsible for elimination of the virus.
So what is responsible for elimination of the virus? Luckily enough, we have a number of brilliant scientists, independent brilliant scientists that have now increasingly been showing, and there is increasing evidence that what in fact is happening is that NK cells are taking care of virus, so so so NK cells that the virus gets into into these epithelial cells and starts to replicate, but NK cells get activated and they will kill, they will kill the cell.
You know in which the the virus right so to replicate. So I was saying that the virus needs to rely on a living cell, so you kill that cell It’s gone It’s all over. So while we are in pollution, we have this solution in in the pathogenesis, because some people eliminate it.
Philip: Absolutely. I just wanted to clarify, because when you said NK cells, somebody may not quite know what you mean, so you mean Non-Killer cells. So It’s a specific group of whites,
Philip: Natural Killer cells, sorry, yes, Natural Killer cells, a special group of white blood cells that go and take out the virally infected cells. Yes, um! Yes, so yes, you’re right is that, because I have seen from a clinical perspective, very old patients who you would expect to be overwhelmed by the virus and they have a few symptoms and then they’re okay.
So they the body, does manage to get rid of it, in some cases – and so it raises the point that I’ve always been saying is that we haven’t spent enough time understanding how the virus impacts the body and understanding how the pandemic then will impact the world we’ve spent all of our time, just going for solutions, has that been a mistake?
Geert: Of course this has been the you know, the the most the most important mistake. I think I’m not sure many people – and I was part of them so in in all modesty I was part of them, not sure whether many people understand how a natural pandemic develops and why we have this first wave, we have the second wave and we have this third wave and – and I mean these waves of disease and mortality and morbidity, they shift from one population to another.
So I’m saying, for example, the second wave. This was typically also the the case with influenza World War 1, when uh, basically more soldiers, young people, uh, you know, died in the trenches of influenza than than you know from from injuries or whatever.
So first, the elderly, I mean weak immune system, etc. Then it gets to the, the wave of morbidity and mortality to, to the other people, and then it gets back to people who have uh, you know have antibodies. So we, we, we have to understand this first. How does this come? Why, all of a sudden is this, this wave of morbidity and mortality shift for example?
Why are the three waves? How do we, how do we explain this?Also, how does it come that some people are naturally protected and others are not? What are these mechanisms? What are these molecular mechanisms?
Because if you make vaccines and all this thing at the end of the day, this is going to interact at a molecular level, and we have not been understanding this. I was just explaining. We Don’t understand our weapon because we don’t understand that prophylactic vaccines should not be used in the midst of an epidemic.
We don’t understand exactly what the virus is doing. So we go to a war and we don’t know our enemy. We don’t understand the strategy of our enemy and we don’t know how our weapon works. I mean, how is, how is that going to go? We have a fundamental problem to begin with.
Philip: I understand, and I completely accept that, but at the same time I am still thinking that if the governments don’t respond in some way because they have to be seen to be doing something um what they seem to be in a lose-lose situation, if they don’t do anything, they’re going to be criticized and if they do do something they’re going to be criticized, Is that a fair statement to make?
Geert: I don’t think so? What was this odd of uh? What’s the name of the guy Hippocrates, you know the first do no harm okay. Well, I mean it wouldn’t matter. If you, if you start vaccinating people, and even it doesn’t work problem, is that we induce a long-lived, antibody response and, as a matter of fact, we know I mean that is not my knowledge. It’s all published problem is that we we failed to put the pieces of the puzzle together.
Fact is that these long-lived antibodies, which have high specificity, of course for the for for the virus they out, compete our natural antibodies because their natural antibodies, they have a very broad spectrum, but they have low affinity right and so by doing this, even if your antibodies don’t work anymore, because there is resistance, or you know that the strains are too different from the original strain.
We still this antibody specific antibody will still continue to out compete your natural antibodies, and that is a huge problem, because I was saying just a few minutes ago, these natural antibodies, they provide you with broad protection.
This protection is yes, it is variant, non-specific, doesn’t matter what variant you get. It doesn’t even matter what type of corona virus is coming in. They will protect you unless, of course, you suppress this level of innate immunity or it is, for example, out-competed by uh long-lived specific antibodies, and so It’s not like, okay, you know you you, you missed it uh…
Okay, let’s try again! No you did some harm. I mean this is different from drugs immunizing somebody is installing a new software on your computer. Don’t forget, I mean these antibodies, they will be recalled every single time. You are encountering a corona virus right. I mean you cannot just erase this, so this is very serious. This is very serious.
Philip: So this is an important point, because when I was looking at some of the research around the challenges that they faced with the initial Sars, the first epidemic and they tried to develop the vaccines one of the things they found, certainly when they tested it on the ferrets was that when they exposed them to a corona virus again, they got a very severe response to it. Is this what you’re saying that we are putting ourselves in a position where we can then have much more severe disease even to viruses that should normally be quite benign?
Geert: Well, you know you, you see all my passion and my conviction, but I mean I’ve been the last to criticize the vaccines uh in terms of, would they in some regard? Could they in some regard be unsafe? Because you know you would have even this exacerbation of disease uh due to antibodies that doesn’t match uh very well with the corona virus they’re exposed to etc.
I know there is three reports on this and there is a lot of uh, you know serious thoughts about this. But um, I think what we are talking about right now, the really the, the, the epidemic or the pandemic problem of having a population that is at no point during the pandemic and to large extent, due to our intervention, has not a strong immune response. I mean this is already serious enough.
This is, this is more concerning than one or the other adverse event that could maybe elicit it uh, I’m not done playing it, but that could maybe be elicited, because people have antibodies that do no longer match very well with the strain they were or with the strain they are exposed to and therefore you know they build a complex, they don’t neutralize the virus, they build the complex and this complex could maybe even enhance viral entry into susceptible cells and hence little exacerbation of disease.
I mean this may be possible, but the problem I’m talking about is a global, a global problem. It’s not an individual, getting an adverse event. It’s a global problem of you know making this virus increasingly infectious, because we leave it all the time, a chance, an opportunity to escape the immune system and to drive this so to whip this up, you know up to a level where the virus is so infectious that we can even no longer control it.
Because I mean these highly infectious strains people some people think. Oh, the virus is going to calm down and it will insert a number of mutations. You know just to be gentle and and kind with us. That’s not going to happen. I mean this highly infectious training remain.
It is not going to be spontaneous mutations that all of a, of a sudden, uh, would become, you know, would, would make these fighters again harmless. Because such a virus would have a competitive disadvantage, could no longer, could not be dominant anymore. So That’s not going to happen, so we’re talking about a very, very, very serious problem here.
Philip: So it I’ve seen the question many times and quite frankly, I get asked the questions. Um we’re coming to a point where people are going to have to take these vaccines. That looks as though It’s the reality, either in the context of work or in the context of travel based on what you’re saying they’re in a lose-lose situation. What does what does this mean?
Geert: Well, what does this mean is very clear. It’s very clear what this is going to mean, so, let’s consider the consequences of this boat at the population level and at an individual level. Because I would well understand if it for the population is maybe not the best thing to do. But you know on an individual level, It’s still okay, yeah. Then It’s not an easy. That’s not an easy question, but as a matter of fact, it’s exactly the opposite.
Well, It’s not the opposite. It is detrimental both on a population level as on an individual level, and I’m telling you why I think the population level I explained you, we are increasingly facing highly infectious strains that already right now we cannot control, because, basically, what we are doing is that we are turning when we vaccinate somebody, we are turning this person into a potential asymptomatic carrier that is shedding the virus.
But at an individual level, I just told you that if you have these antibodies and at some point and I’m sure these will people can challenge me on this, but you know reality will prove it.
I think we are very close to vaccine resistance right now and It’s not for nothing that already people start developing. You know new vaccines against strains, etc. But what I was saying is that, okay, if you miss the shoot, okay, you could say nothing has happened. No, you are at the same time losing the most precious part of your immune system that you could ever imagine of, and that is your innate immune system.
Because the innate antibodies, the natural antibodies, the secretory IGM’s, will be out competed by this antigen-specific antibodies for binding to the virus, and that will be long-lived. That is a long-life suppression and you lose every protection against any viral variant or, or corona virus variant, etc. So this means that you’re left just with no, no single immune response with you, you’re, you know you, it’s known, your immunity has become null, it’s it’s all done.
The antibodies Don’t work anymore and your your innate immunity has been completely bypassed. And, and this, and this while highly infectious strains are circulating. So I mean, if that isn’t clear enough, I really don’t get it and people, please do read my, my, you know what I posted, because it’s science, it’s pure science, pure science and and as everybody knows, I’m a highly passionate vaccine guy right and – and I have no criticism on the vaccines. But please use the right vaccine at the right place and Don’t use it in the heat of a pandemic on millions of millions of people.
We are going to pay a huge price for this and I’m becoming emotional, because I’m thinking of my children of the younger generation, I mean It’s, It’s just impossible, what we are doing, we don’t understand the pandemic.
We have been, we have been turning it in an artificial pandemic who can explain who can explain where, all of a sudden, all this highly infectious strain come from, nobody can explain this. I can explain it, but we have not been seeing this during previous pandemics during natural pandemics.
We have not been seen it because at every single time there was the immunity was low enough so that the virus didn’t need to escape so back at the end of the pandemic. When things calmed down – and it was herd immunity – it was still the same virus recirculating.
What we are now doing is that we are really chasing this virus and it becomes all you know increasingly infectious, and I mean this is just a situation that is completely completely uh completely out of control. So It’s also we, we, we are now getting plenty of asymptomatic shedders.
You know people who the virus, because if they are vaccinated or they have even antibodies from previous disease, they can no longer control these highly infectious variants. So how does that come? Does anybody still understand the curves? I see all these top scientists looking at these curves at these waves, like somebody else, is looking at the currency rates at the stock market. All they can say is, oh, it goes up, It’s It’s stabilizing, it may go down, may go up, etc.
I mean that is not science, they don’t have any glue, they don’t even know whether the curve is going to go up exponentially or whether it’s going to go down or whatever. They’re completely lost, and that is extremely scary. That has been the point where I said, Okay, guys, you have, you have to analyze you have to, but you know these people are not listening, that is the problem.
Philip: So you are, in effect, putting your reputation on the line, because you feel so passionately about this, because I guarantee you that no government, no um no health system is going to want to hear what you are saying. You are, in effect um, almost giving fuel to the fire for an anti-vaxxer who doesn’t want the vaccine.
Geert: No, no, well, no, no, not yet, but because I, i’ve clearly also um addressed uh some emails from anti-vaxxers. I mean I’m not interested, but I’m clearly uh telling them that um you know it at this point at this point, it’s so irrelevant, you know whether you’re a pro-vaxxer or an anti-vaxxer, etc. It is about the science, it’s about, it’s about humanity right, I mean, let’s, let’s not lose our time now with you know, criticizing people or or you know, I mean anti-vaxxer,
Okay, if you’re not an anti-vaxxer, you could be a stalker, you could be, you know we like to stigmatize, because if you stigmatize people, you don’t need to bother about them anymore. Oh this guy’s, an anti-vaxxer. Okay, I mean he’s out of of the scope. Oh he’s a stalker he’s out of the scope.
I mean that what is a discussion that is completely irrelevant at this point, it is about humanity and, of course, I’m passionate. Of course I mean It’s about, It’s about your children, It’s your family, It’s my family, It’s everyone right, and It’s simply for me. I put everything at stake because I’ve done my homework right and this is simply a moral obligation, a moral obligation right.
Philip: Wow wow I mean I, I there’s very little one can say, as I said when you position, that you are in the business of developing vaccines and helping societies protect against infections through the use of vaccines, and in this circumstance you are saying hold it we’re doing the wrong thing here. It’s very difficult to not listen to that, that’s the, that’s the truth.
Geert: Well, the answer is very easy. I mean this is human behavior, you know? We, if we have, if we are, you know having panic, we do something and we try to make ourselves believe that it is the right thing to do till, you know, there is complete chaos and there is a complete disaster and then people say well, you know I mean yeah, politicians will probably say, you know, we have been advised by the scientists and scientists.
You know will maybe point to somebody else, but this is now a situation. I’m asking every single scientist to scrutinize to look what I’m writing to do, to do the the science and to study exactly the, I call this the immune pathogenesis of the disease and because you know, I mean. I like, I like people to do to do their homework, and if the science is wrong, you know, if I’m proven wrong, I will admit it.
But I can tell you I’m not putting my career, my reputation at stake, I would not do this, whether when I would not be 200%, you know, convinced – and It’s not about me not about me at all. It’s about humanity.
People Don’t understand what is currently going on and we have an obligation to explain this and I posted my paper on Linkedin and I invite all independent scientists please to look at it, because this can be easily understood by microbiologists immunologists geneticists. You know plenty of you know, biochemists, etc, etc. All the biologists all these people who have elementary knowledge, It’s not rocket science, elementary knowledge of biology, should be able to understand this, and I mean I can only appeal to these people. You know to stand up as independent scientists and to voice you know their opinion.
Philip: Yes, yes, yes, I mean that was a long point that somebody put on about the innate immune response. Um uh over the falls over reacting of the innate immune response, leading to detrimental effects on other in other corona viruses. So I,I think, you’ve expressed this so well Geert. Is that um?
I think that just hearing your explanation, the passion, the focus on the science – I think that That’s as much as you can do, I think that umI Don’t even want to say anymore, because I don’t want to lose that passion that you have just expressed. How much you are doing in terms of trying to see if you can make a difference with regards to the impact that we are having in this pandemic?
You know we really really appreciate that Geert. We really really appreciate that. I hope enough people um shares this listens to it, certainly because I’m connected with a lot of scientists, please um connect with Geert, take a look at his paper and um and see what you think and, as you said, let’s make decisions based on science. That’s the best that we can do at this point. Wonderful just stay on the line there we’re just going to close off now Geert.
So, thank you again very very much Geert and I hope maybe we can speak again in the near future to expand a little bit further on what you have said.
Geert: Thanks Philip for having me on.
Philip: Wonderful.
FauXci Tick
My Opinion of Dr Fauci has ABSOLUTELY NOTHING to do with Dr Geert Vanden Bossche or Dr Philip McMillan, I’m simply expressing what doctors who still adhere to their Hippocratic Oaths still sound like.
Pretty Incredible! Dr Geert Vanden Bossche is an EXPERT, the kind that Dr. FauXci wishes he was. Dr. Geert Vanden Bosshe is to Dr. FauXci, what a GIANT is to a blood sucking Fauci tick.