“I think the reason why everybody is here is we have a sense that something very bad is going on in the world.”
Okay? Then, when the first man who took the vaccine, he took shot one, shot two, when he died in Germany and had an autopsy, the question was: where is the spike protein being produced in the body? And that’s when that autopsy hit and it was in the brain. It was in the heart. It was in all the essential organs. We knew we were in trouble. We knew we were in trouble.
IN A recent lecture titled ‘Covid-19 Vaccine Safety and Pivot to Early Treatment: Risks of Scientific Censorship and Reprisal’, and a veritable tour de force, Dr Peter McCullough described his emerging understanding of the ‘catastrophe’ of Covid-19 ‘gene-transfer’ vaccines, the ‘loaded weapon’ of the spike protein they produce, and the high effectiveness of early Covid treatments, tragically denied by governments.
The video of the lecture can be seen here, with a summary provided by Cracknewz.
Today we publish the first section of our edited transcript (subsequent parts will follow over the rest of the week) in which Dr McCullough expresses his deep sense of unease at the stripping of his academic titles and at the inexplicable and unprecedented absence of any safety precautions or monitoring of the novel emergency authorised vaccines.
I think the reason why everybody is here is we have a sense that something very bad is going on in the world. And I’m here to tell you, I think it is. And . . . it’s influencing all of us, each and every one of us. And it may have started a long time ago. I’m not an expert on this at all, and I know people are working on this. But somehow we’ve all been drawn into this and it’s affecting us. And I think we all have a sense of urgency that now’s the time, now’s the time when things look relatively normal around us in terms of the bricks and mortar and our social structures and our employment, it’s relatively normal now. And I think all of us have a sense it’s not going to be normal soon with the pace that things are moving. So now’s the time, everyone’s asking what can they do? If you feel tension right now and you feel some emotional distress, and if you feel as if things aren’t going right . . . right now, I think your perceptions are correct. And if your perceptions are correct, now’s the time for action.
I’ve recently taken a position as a chief medical adviser for the Truth for Health Foundation, which is a foundation centred out of Tucson, Arizona, which is dedicated to exactly what we’re doing right now. I am the president of the Cardiorenal Society of America, and I’ve been the president for five years. I helped form that organisation. I donated to it. I think I’m going to be stripped of that title with . . . within a week. I’m the editor-in-chief of Reviews in Cardiovascular Medicine. I think I will be stripped of that within a month. Today, I was stripped of the editorship of Cardiorenal Medicine, a Swiss-based journal. And in the last year, I have lost my job at a major health system with no explanation and no due process. I’ve been stripped of every title that I’ve ever had in that institution. I’ve received a threat letter from the American College of Physicians . . .
So whatever’s happening is happening [is] because of our efforts to have some scientific interchange. We are participating in a topic of public importance – that’s the reason why every table [here] is full. What we are doing is lawful. What’s not lawful and what’s not right is what’s happening with respect to censorship and the threat of reprisal.
I’m the senior associate editor of American Journal of Cardiology and if Bill Roberts can keep me in there, I’ll hang in there. My tagline is America Out Loud, talk radio. . . . I am from Texas originally, I went to Baylor University undergraduate, then UT Southwestern. I went on to the University of Washington in Seattle. I came to Michigan. I did three years of general internal medicine actually in Grayling area to pay back my student loans . . . And then I went to University of Michigan School of Public Health and got my Master’s degree in epidemiology. I was kind of trained to do this public health work. I joined Beaumont Hospital under Dr Joel Kahn and Bill O’Neill, and I trained in cardiology. I took my first job at Henry Ford, was the programme director at Henry Ford, became the Chief of Cardiology at the University of Missouri in Kansas City. Returned to Beaumont, was a division chief for a long time. Was the chief academic scientific officer for St John Providence Health System and then moved on. I wanted to finish up down in Texas and I held wonderful positions in Texas.
But I’m not new to the national scene. Even early on when I was at Henry Ford, I was on President Clinton’s advisory panel to health care. When I was at Beaumont, I testified in front of the Congressional Oversight Panel regarding a product label expansion of drugs, and I was on C-SPAN for seven hours getting fried by the senators. So I wasn’t new to this. But what’s new to me now is to be in a position of – and I’ll take it – of authority. OK, I’ll take it because somebody has to. [applause from audience]
I had a window last year when this whole thing started, I had a window to America through a Republican journal, The Hill. And I’m kind of a middle of the road person. I’m not a really hardcore right winger, but The Hill took me and I was a regular contributor to The Hill. And then I changed over and actually started my own radio programme on America Out Loud talk radio, The McCullough Report, because I needed the window. In our medical field, we publish in journals to each other, doctors and scientists. We talk to each other. But the public is largely excluded from that big conversation.
And our journal publications are slow. We’re talking two to five years to get something in print. You know, this thing hit us. We needed to get now. We needed to get things published now. We needed speed because it’s a mass casualty situation. So that’s what this is all about. These letters behind my name, I predict, will be progressively erased. I took one off there this week. It’s going to happen. It’s going to happen because there’s powerful forces at work, far more powerful than we can possibly think of, that are influencing anybody who is in a position of authority. And I already told you, I’m going to take authority.
So the first authoritative position I’m going to take is this: as an American and as a consumer, for new biologic products, demand safety, safety, safety . . . safety . . . We have a situation where there has been an injection of a substance into half of Americans’ bodies. And there’s yet to be a report to America on (its) safety. Astonishing.
Well, it wasn’t the case back in 1976, there’s Gerald Ford getting his swine flu vaccine, right, swine flu in 1976. We got to 25 deaths, 550 cases of Guillain-Barré syndrome, which is ascending paralysis. There were 55million Americans vaccinated, 220million people in the country at that time. [They] shut it down. Not safe. It was very transparent. Americans were watching. Sure, there was some controversy: were the deaths related, not related? It didn’t matter. Unexplained deaths didn’t matter. Shut down the programme. [It was] not safe. It was considered a debacle . . . and it went down as a debacle . . .
In my view, we’ve been gambling. We’ve watched a gamble go on in our country. And the gamble has gone like this: this virus came in and we’re going to test out some new tech, and we’re going to gamble with, not just America, we’re going to gamble with the world. This is a gamble of extraordinary, extraordinary implications. We didn’t have to and we don’t have to, but we did. And this is the gamble. The gamble is genetic gene transfer technology. The FDA considers the current American vaccines Pfizer, Moderna, Johnson & Johnson as gene transfer tech. That’s what it is, it’s gene transfer tech.
There were 24 of these platforms that have been around for decades. They were all designed to transfer genetic information. Most of the time, just to transfer in the RNA to produce a missing protein. For instance, a deficiency disease called Fabry disease, a deficiency of α-galactosidase. I ran the programme in Dallas on this, an interesting medical problem. But it was just simply a way of producing their deficient enzyme. Seems pretty harmless, right? Give the cells an injection of messenger RNA about once a month, maybe once every three months, and then the body could make this needed protein. Okay? There’s been other ones. There’s been attempts in heart failure, in cancer. The only messenger RNA gene transfer technology drug that’s on the market is called Patisiran, and that is a drug that produces a small interfering messenger RNA that interferes with the production of what’s called transthyretin, which is a protein that causes amyloidosis, which is a medical condition.
So we actually do have one of these on the market, but there’s 24 others that have largely been losers, and they’ve been losers in many ways because they couldn’t produce enough of the deficient protein, or they couldn’t actually be reverse transcribed and produced the gene that’s needed to install on the genome.
But these were ready to go, and the adenoviral DNA shown on the left of the screen here. That’s Johnson & Johnson. So that’s an adenoviral vector where these replication incompetent virions come in and they inject DNA into the cytoplasm. The DNA is taken up into the nucleus. From the nucleus, the messenger RNA for the Wuhan spike protein is produced. That messenger RNA then produces the spike protein. But because it’s not a synthetic RNA, it actually is digested within RNA [unclear]. But the issue is, there’s so much of the DNA that goes into the nucleus, there is so much of its persistent effect that Johnson & Johnson can basically get by with one shot, which is amazing. So it is a ton, I can tell you right now, from a genetic perspective, it’s a ton of material that’s going into the human body.
With the messenger RNA vaccines, Pfizer and Moderna are different. These are synthetic messenger RNAs. They have what’s called a nucleoside analogue cap at the three prime and five prime end. And those caps are sturdy. Normally, a messenger RNA is used once it’s disposed of – used, once disposed of. This one is used over and over and over again and stays in the cells for a long time. We don’t know how long, but it looks long. It looks very long.
And we are working with scientists all over the world. And there is a belief now that the messenger RNA can survive cell division so a parent cell can give it to daughter cells. And it looks like the messenger RNA can actually be transferred in little packets called microsomes to other cells. So it’s not just a mosaic of cells that gets the messenger RNA. It may be much more proliferative than that. And the messenger RNA itself is used over and over again to produce the spike protein. The spike protein is the little red characters there. And when they’re expressed on the cell surface, that’s an abnormal protein.
For the first time in human history, we have a biologic product that’s telling our body to produce an abnormal protein. You know, the design of this was to produce a normal protein, but this is to produce an abnormal protein. It’s not just an abnormal protein, it’s the [unclear] or the spine on the surface of the virus. The virus is the ball. The little spines, you’ve seen a million cartoons of it, that’s the spike protein. 1,200 amino acids, probably about eight to 12 glycosylation sites and two major segments to it, S1 in S2 and what connects them is what’s called the furin cleavage joint.
The furin cleavage joint is what was manipulated, we believe, with gain of function research in the lab in China. So in this little red character here, which looks pretty benign, it is kind of a loaded weapon, if you will. And what I mean by weapon, it’s now known that the spike protein itself is independently pathogenic. It causes damage itself, okay? And I think everyone accepts this. When I mean damage, it damages the cells in which it’s produced. When it’s on the cell surface, the body immediately recognises it’s not supposed to be there and attacks. When the spike protein breaks free, which it does, it circulates in the human body for about two weeks. In a paper by Ogata and colleagues – this is being filmed and this is going to be fact-checked, so I want the fact-checkers to see that – Ogata et al, Harvard circulates in measurable and plasma for two weeks after a messenger RNA vaccination. After the second shot, it’s no longer measurable, probably because the antibodies produced dampen it down. It doesn’t mean the spike protein is gone. We don’t know how long the cells produce the abnormal spike protein.
It would have been wonderful if the spike protein just stayed in the arm. If the deposit, the 1cc injection in the arm, and if the production of the spike protein would have just stayed in the arm and the immune reaction stay in the arm, that would have been, I think, the best possible scenario for these vaccines. Not the case. When the Ogata paper broke, everyone said, ‘Oh boy, now the spike protein is circulating.’ Okay? Then, when the first man who took the vaccine, he took shot one, shot two, when he died in Germany and had an autopsy, the question was: where is the spike protein being produced in the body? And that’s when that autopsy hit and it was in the brain. It was in the heart. It was in all the essential organs. We knew we were in trouble. We knew we were in trouble.
Never once did we have a vaccine or any injection in the human body that got distributed via lipid nanoparticles throughout the body within a matter of weeks and then set up shop to produce a damaging protein. This protein circulates. It damages organs. It damages endothelial cells. Blood cells. It causes blood clotting. There is a wealth of scientific papers on this. There’s nothing about the spike protein that’s good. These little red characters here on the slide are lethal. They’re lethal.
They play a part in the fatal nature of the natural infection. And the Chinese have published a ton of studies on this. Everything we learn about the spike protein is bad. There’s a paper now showing the spike protein interacts strongly with the p53 and the BRCA genes, which are the cancer genes in the human body.
Now, if you’re going to have spike protein for a day or two, a week or two, probably not a big deal, but if you’re going to have a spike protein on shot one and shot two and shot three and shot four, in year one, in year two, in year three, who can imagine what’s going to happen to the human body? How many runs can a human body take with a potentially lethal pathogenic spike protein that was manipulated in a lab in Wuhan, China, and now available for human consumption by injection across the world?
That’s what we know about these vaccines. Everything we know about it, you would agree, is a dangerous mechanism of action. We’re late on this, we’re late, but we got this in press, Bruno and colleagues, 57 authors, 17 countries, where the title of the paper is ‘SARS-CoV-2 Mass Vaccination: Urgent Questions On Safety’. Highlighted parts there: if we don’t have safety boards, data safety monitoring boards, critical event committees, human ethics committees assigned to these programmes, we have no hope of shutting this down or even evaluating for safety.
I’ve chaired over 24 data safety monitoring boards. I chair two for the National Institutes of Health right now. I know what I’m talking about. I know about data. I have over 650 publications in the National Library of Medicine, 45 on Covid. I’ve reviewed more reports and made more inferences on scientific data, I think, than anybody in the world right now and certainly in my field – in heart and kidney disease – in history. I’m not fooling around when I say our governments owed it to us from the beginning to have a data safety monitoring board. Where’s the DSMB? The data safety monitoring board is an independent group of experts without a stake in the outcome. The sponsors of the US programme are the FDA, the CDC and then, behind them, Pfizer, Moderna and J&J. None of those entities are qualified or capable or even ethically charged to evaluate mortality or outcomes. They personally have a stake in the outcome of this. We never let the company decide on causality of a problem. We never let a company tell us if a product is safe. We always have external bodies.
And by the way, when these came through the clinical trials, there were data safety monitoring boards. And over two months, when they select relatively healthy populations, they did look okay after two months. The problem is, once they got broadly used in the population, we realised, holy smokes, we not only don’t have a data safety monitoring board – you know everyone’s asked to sign the consent form, saying they’re in a clinical investigation, it does say that – we actually didn’t have any guard-rails on this to . . . if a problem was there, to be able to tell America and tell the world, ‘Listen, we’ve got a problem. We’ve got to do something about it.’ Okay? We didn’t have the fundamental safety mechanism.
Historians will write about this. Okay? This is kind of like Tuskegee. There was a terrible experiment, there’s been terrible historical things. Not having a data safety monitoring board will go down in history as a colossal mis-step in public health. How in the world can we take the sponsors of the programme – the FDA, the CDC, Pfizer, Moderna – and let them be in charge of safety? And even worse, how can we let them not ever produce a safety report, never do a safety press briefing? Nothing.
The messenger RNA or adenoviral DNA, the production of the spike protein is a dangerous mechanism of action. It injures cells, tissues and organ and endothelial damage, and we have papers to support that all the way. The spike protein circulates at least for two weeks. Body fluid, donated blood, that explains the shedding events that . . . you know so well. No genotoxicity, teratogenicity or oncogenicity studies. They wouldn’t be needed for vaccines from a regulatory perspective, but they would for gene transfer technologies.
There’s a concerning reduced fertility study by Moderna submitted to the European Medical Association. Fertility did go down in animals. It wasn’t a huge drop, but it was real. There was a concerning biodistribution study, Pfizer in Japan, where the lipid nanoparticles hyper-concentrated in the ovaries. As the Chinese had shown us a couple of years earlier with a paper by Ning and colleagues. As I mentioned, there are no safety committees. No restriction of properly excluded patients from the trials.
When the trials were done, they properly excluded the FDA, Pfizer, Moderna and J&J, for a reason. Exclusions must be justified with all the regulatory authorities and the Office for Human Research Protections for a reason. Pregnant women, women of childbearing potential who cannot not guarantee contraception, Covid-recovered, suspected Covid-recovered, those with severe allergies. Why are they excluded? You have to justify it. The two reasons to exclude patients from clinical trials is: no opportunity for benefit and excess opportunity for harm. And these groups were excluded.
When we finish a study and a drug is on the market, we never just let the excluded groups get the drug on a whim. Or, ‘Why don’t we just try it out now?’ There’s never been a drug where we say, ‘You know, we kept pregnant women out of it. It could be dangerous. Let’s just go ahead and give it to them.’ Never. That should be an alarm bell. The behaviour of doctors and the American College of Obstetrics and Gynaecology that says to vaccinate women with no randomised trials safety data ought to be a giant alarm bell going off.
Alarming. That’s a bellwether. Pregnant women and the foetus are the special situation in medicine. We have pregnancy categories for this. We bend over backwards. We only use drugs where we have lots of years of experience. We know they’re safe in pregnant women. We only allow inactivated flu, tetanus and pertussis, all inactivated. That’s it. That’s it. And I published an opinion editorial . . . where I said, ‘Listen, this is pregnancy Category X. Any new seizure drug, any new diabetes drug – no different, no different. This should be alarming.’
I have a lot of interaction with doctors. I don’t have a single doctor who can look me in the eye and support what’s being done to pregnant women. What I see in their eyes is fear, shame, guilt. They know they’re wrong, but they’re confused, and they can’t seem to understand why they’re wrong. Doctors and those with them – and there’s a lot with them – are in a trance right now. They’re in a trance. They’re in a mass psychosis. And it’s worldwide.
Tomorrow Dr McCullough expands on his deep concern at the lack of any system at all to protect the American people against vaccine damage, that is already well above the level which, by historical standards, should have shut down the programme