W.H.O. / Governments Working in Collusion with Big Pharma? | A Necessary Look Back at the Swine Flu Pandemic

STEPPING BACK IN TIME: Another attempt to vaccinate the whole world.

It is extremely important to learn about our history, because as this year has shown, not recognizing the troubles and past circumstances – especially when dealing with our very lives and those of our loved ones – is causing untold turmoil and unnecessary deaths/injuries.
 
The below video is an insightful and historic account of how quickly we forget (and/or didn’t realize) about what happened in the not-so-distant past. I would highly, highly suggest checking it out and sharing. It is CRUCIAL to understand the events that have led up to the situation we see ourselves in today. We must learn to recognize attacks on not only our health, but also our whole livelihood.

I have highlighted some key parts of it below, but the whole video is well worth the watch. Do the events sound familiar to you? What if we replaced the word “swine flu/h1n1/influenza” with “coronavirus”? This video is an eerie look back at the 2009 events and the goal, even at that time – 12 years ago – of the exact same thing we’re seeing today. It was never about the “virus”; and it was never about our health.

Source: odysee | Do You See What I See Productions | A-Necessary-Look-Back-at-the-Swine-Flu-Plandemic

Some embellishment has been added for emphasis:

“So what is technically a biological weapon is being sold to us as a prophylactic, and if we don’t take it voluntarily, if we don’t believe in the hysteria of the Media, we are finally forced to take it.”

[00:00-00:18] Jane Bürgermeister 2009: “After this health crisis, a new political force will be installed.

It will be the World Health Organization, the one in charge of organizing the enforcement of these things, also the U.N.”

[00:35-04:52] Jane Bürgermeister 2009: “And it will happen at the same time, more or less, in parallel in all countries, because all countries follow the same schedule for voluntary vaccinations.”

“And after this period, every government estate will be joined into a single, new structure, that will incorporate itself under the W.H.O. and U.N.”

(Some politicians have already suggested) “that the W.H.O. should be the natural global health authority. There are other clear plans for the creation of a world government. And the pandemic seems to be the means to this goal, the same as this vaccine also an instrument is, to fulfill that old dream of a single world power.

What I am stating here is that there is a secret biological war going on, an undeclared biological warfare against civilians is being waged, because it is carried out by a small group, against a larger majority of billions of people, carried out with cunning and deception.

So what is technically a biological weapon is being sold to us as prophylactic, and if we don’t take it voluntarily, if we don’t believe the hysteria of the Media, we are finally forced to take it.

What we see is the World Health Organization trying to succeed in enforcing vaccination on all people, a system according to which they’ll keep data about all people for the rest of their lives.”

“At meetings, many governments deny that they intend this, they state that it will be voluntary and so on, but all the while they are building the infrastructure for forced vaccinations.”

“You might say, “How is something like this possible?” “How can our health officials do this?” “What are health safety institutions doing, the Media…” “How can every security step be failing us?”

I believe this plan has been thought over many, many years. And unfortunately, many officials were “bought”. 

We have to accept that officials in charge of protecting people are actually not giving warnings and they let these things happen.

If I could have access to the documents of my research, then also they could.”

“An important role in this sad story is played by Media; as I said, I have learned myself that the important information never comes from Media, and as credible as it sounds, I have seen for myself how systematically it’s just a propaganda instrument.”

“Exactly because Media doesn’t report some essential facts, and instead just goes over trivial everyday stories, most people are absolutely clueless about what’s going on here.”

“It’s up now for each citizen to say: I will influence political events – “

Setting the stage for the Media hysteria

[05:44-06:35] WHO Director General, Dr. Margaret Chan: “On the basis of available evidence, and these expert assessments of the evidence, the scientific criteria for an influenza pandemic have been met.

I have therefore, decided to raise the level of influenza pandemic alert from phase 5 to phase 6. The world is now at the start of the 2009 influenza pandemic.

Influenza pandemics, whether moderate or severe, are remarkable events. Because of the almost universal susceptibility of the world’s population to infection.

We are all in this together.”

Essentially impossible to distinguish between regular seasonal flu vs. 2009 H1N1 influenza

[06:59-07:47] : How can a person tell if they have the regular flu seasonal flu or if they’ve contracted the 2009 H1N1 influenza virus?

Anthony Fauci:Well, for a person, him or herself to be able to determine that, would essentially be impossible, because you can get everything from very very mild illness to severe illness with either seasonal flu or the H1N1 new 2009 pandemic flu. Most of the time it’s a mild disease, but there are unusual cases that can be severe. The only way a person can tell is if they get their blood drawn or other laboratory tests, which could specifically distinguish between one and the other. But that is something that is not done routinely.”

Role-playing? News anchor and correspondent look amused while discussing if they had swine flu. /
Also, “testing really doesn’t matter”

[07:48-10:26] Anderson Cooper: “As of tonight, more than 41,000 Americans have been infected with an H1N1 or swine flu virus. Maybe you know someone who’s come down with it.

We do. Our very own Sanjay Gupta. Our chief medical correspondent got the virus during a recent trip to Afghanistan. Sanjay said it was the sickest he’s ever been. He joins us now to talk about it; he’s a physician and a patient – Uh, Sanjay, first of all, how do you feel now?”

Sanjay Gupta: “You know, I feel fine, now, Anderson. And you know, it’s worth pointing out, you and I talked about this while we were both in Afghanistan, and you were quite sick as well. I’ve come to find out later on that the H1N1, the swine flu as it’s called, was circulating quite a bit, Anderson, in the area that we were in.”

Anderson Cooper: “Was it really? No one mentioned that to us. Or at least not me.”

Sanjay Gupta: “I know, I mean, you know, frankly speaking, we can talk about this now via satellite but you know, there’s a good chance, based on everything that I’m hearing, that you also had H1N1 virus infection.”

Anderson Cooper: “Well, cause I – I mean, I had similar symptoms to you, I was – the cough was the worst cough I’ve ever had, and it even hurt my heart when I was coughing, and I went to you, and you were really sick, and I asked you, “Is it possible it’s swine flu?” And you said, “Probably not, because usually swine flu has a very high fever right away.”

Sanjay Gupta: “That’s right. And you know, it’s interesting because I think the next day, I think maybe you had gone to a different province and I, I was feeling miserable the next day and I hadn’t checked my temperature, you know; you’re in the desert, it’s hot outside. Hadn’t really thought about it. I went there and my temperature was around 102 degrees, so, you know, pretty high for certainly for me, 98 being normal and 98.6.

So that was the first sign and then, you know, I had that same cough that you did. Light-headedness, and I was freezing cold. I don’t know if you had that as well. [Anderson Cooper: “Yeah.”] But that was really the most memorable part of it. I was freezing cold despite being in the desert.

Are you coughing right now?”

Anderson Cooper: “I- I’m still coughing. I will say. Just a little bit.”

Sanjay Gupta: “Thought I just heard that, yeah. I have a little bit of a cough as well. I don’t think we’re contagious though.”

Anderson Cooper: “I love that I just learned that I may have had swine flu from you, via satellite. Um, but what was it like? I mean, it was for you, you said it was the worst, worst sickness you ever had?”

Sanjay Gupta: “It really was. And I don’t get sick very often. I mean, I can’t remember the last time I was sick. I don’t remember the last time I had the flu. But this really floored me.

I think the day after you and I talked about it, the next morning, I was trying to get out of my sleeping bag, I could barely take a couple of steps without feeling really light-headed. And again, those just profound chills and shakes, despite the fact that it was over a hundred degrees outside. And then when I went to the – I went to the clinic, they had a role, it’s a role three battlefield clinic. You know, they gave me some IV fluids cause I hadn’t eaten in a while, and they also did the swab.

What we know is that H1N1 is circulating around the world. You mentioned how many cases have already been, Anderson, and what most doctors have told me, most infectious disease doctors, is that the testing really doesn’t matter.

Fauci, director of NIAID, suggests to vaccinate highly vulnerable groups such as pregnant women and children as young as 6 months old

[13:25-14:32]: This year, do I get a shot for the 2009 H1N1 flu in addition to the regular flu shot?

Anthony Fauci: “Well, you certainly should get your seasonal flu shot. That’s for sure. When we talk about the vaccination program for the H1N1, we’d like to be sure that the 5 priority groups of individuals get the H1N1 that becomes available early on. We fully expect that we would have enough so that you can cover not only the priority groups, but anyone else who feels they want it and need it. So the answer is, yes you should get the H1N1.

The 5 priority groups are:

pregnant women
– people who are the caretakers, parents or what have you, of children less than 6 months old,
– healthcare workers
young children and young adults from 6 months to 24 years old
– and individuals from 25-64 who have underlying medical conditions that would compromise them”

Vested interests of academics, governments, W.H.O. and drug companies to push unproven vaccinations

[14:32-15:48] News Segment: “In clinical trials on volunteers began on Wednesday in Australia for vaccine against swine flu.

But leading researchers now raising serious questions about the way the world is responding to this pandemic.

Dr. Tom Jefferson says the response to the virus is driven by vested interests. Academics, governments, the World Health Organization, and drug companies who all stand to gain.”

Dr. Tom Jefferson: “By declaring ‘pandemic’, they’ve pushed the button on this juggernaut that they’ve created. And of course, antivirals are part of that, and vaccines are part of that, and the whole panel plays a part of that.

All I’m saying, is let’s act with a little bit of caution and common sense. And let’s look at the evidence, the hard evidence.

Until they actually get used, we do not know whether it will work. Their seasonal counterparts don’t have a very good track record. The evidence from the hundreds of studies that we synthesized, is that sometimes they work a little, and sometimes they don’t.

We’ve been brought up, people in my generation, to understand that a pandemic means deaths and a lot of serious cases. And that seems to have dropped out of sight, and they’re lowering the threshold, of a definition of a ‘pandemic’. And that is not a good thing. In many ways.

Swine flu not much worse than a bad cold. /
Natural immunity would provide better immunity than the vaccine.

[17:09-18:23] [Guest doctor]: “Now 3 months later, and as a GP I’ve seen dozens of cases of swine flu, we can see that overwhelmingly, in healthy adults, it’s a very mild illness. Really not much worse than a bad cold. And you will have to question whether or not once you’ve vaccinate a population against an illness that is no worse than a bad cold.

But remember as well that by the time we get this vaccine here, in the country, a lot of us will have come across the virus anyway. And we’ll have developed natural immunity. So we’ll have better and longer lasting immunity than the vaccine would provide already. Which would make a vaccine completely unnecessary.

As I’ve said, the vaccine is being fast-tracked; it’s being rushed onto the scene and the normal safety tests that are done before a vaccine is introduced will be very, very limited. And the last time that a vaccine was given nationally, against a swine flu pandemic, was in the U.S.A. in 1976. And then after vaccinating millions of people, they stopped that vaccination trial because of an increased rate of side effects. There was something called Guillain-Barré syndrome, a paralyzing disorder. But then so they had to stop the trial. And we don’t know that that’s not going to happen again – “

Children used as guinea pigs /
Mercury found in vaccines linked to autism, brain disorders and Guillain–Barré syndrome

[19:10-21:41] Priya Sridhar: “Joining me to discuss all of this is RT contributor and investigative journalist, Wayne Madsen. Wayne, thanks so much for joining me.

First of all, can you tell me, who has taken the swine flu vaccine so far and what have you heard about it?”

Wayne Madsen: “Well apparently there has been a test community used already. We’re also hearing that the vaccine that’s being developed, they’re saying it’s not for everyone. Apparently, children were used as uh, for lack of a better term, guinea pigs in Oklahoma. I know from talking to people in the research community, even scientists who helped develop the vaccine for smallpox are saying they’re not going to take the vaccine and urging their friends and family not to take this vaccine either.

Priya Sridhar: “And what kind of side effects did these children have, if any?”

Wayne Madsen: “Well, contained in the vaccine is a component called thimerosal,  which has been proven – uh, half of it is composed of mercury. And it’s been proven to cause not only Guillain-Barré syndrome, but also autism, in young children. There’s been several court cases because of past vaccinations due to the autism issue.”

Priya Sridhar: “And so how will the swine flu vaccine be offered? Will it be mandatory for people? What have you heard about that?”

Wayne Madsen: “Well there was a conference here in Washington last week where we have two – two themes present. We have the research community, the medical community, saying, “Look, what we need to provide the public is good information and let them make the decision based on facts.”

We have the emergency community, the Homeland Security, Federal Emergency Management Agency people talking about forced vaccinations, forced quarantines… Basically the politicians running the show instead of the people who are from the medical community and know much better about the threat of this particular influenza.”

Reporter: “While there are fears the U.S. media is covering up the possible side effects of the swine flu trial vaccine, 28,000 human guinea pigs are sent to test the jab. Bad news outlets have so far kept their snouts clean over its link to rare brain disorder.”

Purpose of recalling 800,000 mercury-free vaccines intended for children…

[25:40-28:13] Reporter: “Health officials there are recalling 800,000 swine flu vaccines intended for children. They say their efficiency wears off after a short period of time. Now it comes as vaccination against H1N1 become available to any American who wants it.

Our correspondent Priya Sridhar – Priya, hi. This recall must have some people wondering what the whole point is in taking these vaccines. What is the feeling over there?”

Priya Sridhar: “Hi Kevin. Well, I think people have had reservations about this vaccine for a while. Previous reports showed that the vaccine may have been linked to the Guillain-Barré syndrome, and now this new report is say – causing many people to say, “What is the point?” And so joining me to help talk about this, is co-founder and president of the National Vaccine Information Center, Barbara Loe Fisher. Barbara, thanks so much for joining me.

So tell me about the latest numbers. 800,000 H1N1 vaccines that were supposed to be for children are now being recalled. What do you know about this?”

Barbara Loe Fisher: “Yes. Just this morning, Sanofi Pasteur recalled 800,000 doses of H1N1 vaccine. We think that it’s mercury-free vaccines – the single dose vials. I haven’t confirmed that, but if that’s true that means those children are going to be getting a multi-dose vial of vaccine that contains mercury. And of course mercury is something that a lot of parents in this country have been very concerned about giving their children through vaccination.

And, the issue is a lot of people in this country are not taking the H1N1 vaccine. There’s going to be potentially a surplus of vaccine that will then have to be disposed of. If it’s in the multi-dose vials that contain mercury, it will have to be disposed of under hazardous materials regulations. HAZMAT regulations. Because you can’t dispose of mercury in this country – mercury containing vaccines, by pouring it down the drain or throwing it into a regular garbage can. You have to undergo hazardous material regulations.”

Priya Sridhar: “And what are some of the concerns with the mercury?”

Barbara Loe Fisher: “Well the mercury has been associated with brain injury in children. Regression in children who have gotten these vaccines. Regressing into autism. It’s very controversial; the government denies that mercury has anything to do with these children’s autism.

But, in 1999, our Environmental Protection Agency and the Food and Drug Administration directed the vaccine manufacturers to take mercury out of childhood vaccines. But the flu vaccine, in multi-dose vials, contains mercury. And so I’m wondering what’s going on here with recalling these 800,000 doses of potentially mercury-free vaccines, and what’s going to happen with children who are going to get the mercury containing vaccines.”

[29:14-29:29] Barbara Loe Fisher: “There have been about 3,700 vaccine adverse events reported to the government, 12 deaths, 10 cases of Guillain-Barré syndrome, but this is only a tiny fraction of what’s actually occuring out there. Because most doctors don’t report vaccine adverse events to the government.

Compilation of news reports of children experiencing tragic side effects from the swine flu vaccine

[30:39-31:46]

Reporter: “6 year old Nikiyah Torres is all smiles now, but her mother Naomi Troy is still fuming about a medical mistake at PS 335 in Brooklyn. When a nurse there mistook Nikiyah for a new student, she was given an H1N1 vaccine, without parental consent.”

Naomi Troy: “She’s not a guinea pig. You don’t make a mistake with children lives.”

Reporter: “He has a lot of questions tonight after he said his son was given the H1N1 vaccination at school, without his permission. The child got the vaccination from Montgomery County Health Officials at Camargo Elementary School. But his dad says the child has other health issues that make this vaccination potentially dangerous.”

Reporter 1: “A Northern Virgina family dealing with a stunning turn of events. Their healthy, athletic son suddenly comes down with a debilitating illness. They believe that it’s connected to a swine flu vaccine he got 24 hours earlier.”

Reporter 2: “Thursday afternoon he got his flu shots. By 10 o’clock Friday morning he had chills and started feeling weak. And by 4 that afternoon, he was having spasms.”

Reporter: “A 4 year old Rochester boy is recovering tonight after nearly dying, after being vaccinated for H1N1.”

3 shots / booster shots recommended… “trust the government and health officials”

[32:31-32:41] Meredith Vieira: “Now you’re asking people to get 3; that’s a tough sell.”

Guest: “Oh, Meredith, I think you hit the nail on the head. This is going to be a public relations, ‘trust your government and your health officials’ public campaign.”

Package insert: “Safety and effectiveness of the H1N1 2009 vaccine have not been established in pregnant women, nursing mothers, or persons less than 18 years of age.”

[33:22-33:43] Deirdre Imus: “There’s 3 major reasons why the H1N1 for children is not safe. They say it right in the package insert, from the manufacturer, it says right here, virus vaccine manufacturer: “Safety and effectiveness of the H1N1 2009 vaccine have not been established in pregnant women, nursing mothers, or persons less than 18 years of age.” They say it right there! In the packaging insert!”

W.H.O.’s loyalty seems to be in pushing vaccines – continues to announce a “pandemic” when there isn’t one

[34:36-38:02] Wolfgang Wodarg [female voice over in English]: “And what I’ve heard from the W.H.O., my concerns have merely been strengthened. The only evidence we’ve heard is that many people were asked and figure was given to us how many people were asked, but no justification were given for the actions undertaken by the W.H.O.

So the core question remains, why was the definition of the pandemic changed? Mr. Fukuda repeated that we had a pandemic underway. That is to say that we have to look at the question as to how a pandemic is declared. And how the fears are then subsequently elate – that is to say, at what point do we say that there’s no longer a pandemic?

In October last year we knew that the flu had run its full course because they are at a season’s removed than we are, so we could observe Australia, the wave had passed, and there was a moreover a trigger which it was said the flu was a trigger which enabled people to be protected from other strains of the flu. So this is something that the W.H.O. knows and the W.H.O. still says ‘we have a pandemic underway, use up all the vaccines that we have in stock’.

I want to read you something, from the Associated Press, the 19th of May, 2009, precisely at the time when the discussions were underway as to what the phase of the pandemic was, [Wolfgang Wodarg in English]: ” – urge the World Health Organization to change its criteria for declaring a pandemic again.” So to take it back what they did. Saying the agency must consider how deadly a virus is, not just how far – not just only how far it spreads across the globe. Fearing a swine flu pandemic declaration could spark mass panic, and economic devastation, Britain, Japan, China and others, asked the global body on Monday to treat carefully before raising this alert.

Some cited the costly and potential risky consequences, such as switching from seasonal to pandemic vaccine. Even though the virus so far appears to be mild. In May already. All those national specialists asked W.H.O. to change the course; to change its direction.

And then, although no formal changes were made on Monday, W.H.O. said it would listen to its members request. ‘And it’s certainly something we look at very closely’, said Dr. Keiji Fukuda, W.H.O.’s flu chief.

This happened, and afterwards, the pandemic was declared on the 11th of June, and the vaccine was sold to everyone and children were vaccinated in vain. I just say this, this is a very serious facts we see and we knew this already when the pandemic was not yet – the alarm was not yet uttered. So I think it’s a very, it’s a very important thing to discuss about the definition of a pandemic.”

Explanation as to why W.H.O. continues to announce a pandemic

[42:40-42:57] Narrator: “Many countries, including Germany, Italy, France and Great Britain, concluded secret agreements with pharmaceutical companies before the swine flu incident. Which obliged them to purchase swine flu vaccinations; but only if the W.H.O. issued a pandemic level 6 alert.”

“Greatest medical scandals of the century”

[45:55-47:44] Jon Snow: “It is one of the greatest medical scandals of the century according to a leading health expert in Brussels. The Council of Europe Health’s Chief has accused major pharmaceutical firms of organizing a campaign of panic and unduly influencing World Health Organization decisions. And with European countries now burdened with bills from millions of unwanted doses, the swine flu vaccine, he wants an investigation.

Our science correspondent, Tom Clarke, has this report.”

Tom Clarke: “64,000 people dead – tens of thousands hospitalized, a country crippled by a virus. The predictions of the impact of swine flu on Britain were grim. The government’s response: spending hundreds of millions of pounds on antiviral drugs and vaccines, adverts, and leaflets. But 10 months into the pandemic, only 355 Britains have died. And globally, the virus hasn’t lived up to our fears.

Were governments misled into preparing for the worst? Politicians in Brussels are now asking for an investigation into the role pharmaceutical companies played in influencing political decisions that led to a swine flu spending spree.”

Dr. Wolfgang Wodarg: “There must be a process to get more transparency out of the decisions and the W.H.O., how they function and who is influencing the decisions of the W.H.O. And what is the role of the pharmaceutical industry there? I’m very suspicious about processes which are behind this pandemic.”

Tom Clarke: “They also want to probe ties between key W.H.O. advisors and drug companies.”

Paul Flynn: “Who is deciding what the risk is? Is it the pharmaceutical companies? Who want to sell drugs? Or is it someone making a decision based on the perceived danger? In this case, it appears that the danger was vastly exaggerated. And was it exaggerated by the pharmaceutical companies in order to make money?”

Are the pharmaceutical companies and W.H.O. running the show?

[47:45-48:01] Bill Dod: ” – will launch a probe into pharmaceutical companies accused of manipulating swine flu data. This follows a claim by a renowned German scientist that vaccine manufacturers pressured the World Health Organization into declaring a swine flu pandemic, seeking to increase profits.

RT’s Laura Emmett has more.”

Laura Emmett: “It was supposed to be a deadly pandemic. But it’s so far nothing more than a serious cold. And it’s left a lasting headache as a debate rages over pharmaceutical companies deliberately misled governments about the seriousness of swine flu to make them stockpile vaccines.”

Paul Flynn: “And I believe when we have a thorough investigation, and we look at this, we’ll discover that that’s the story: the world has been subjected to a stunt, for their own greedy interests of the pharmaceutical companies.”

The H1N1 virus may have started in a lab /
Bioethics? Or Bioterrorism?

[49:30-49:38] Bill Dod: “U.S. investigative journalist and RT contributor Wayne Madsen says he’s gathering more and more evidence that the H1N1 virus started out in a lab.”

[51:16-51:38] Priya Sridhar: ” – how exactly did this happen? This is the 21st century. I mean, how could something – how could these gene sequences get manipulated and then be disseminated throughout the country?”

Wayne Madsen: “Well, apparently what we are seeing is this could have been a product of some over zealous research on the part of the research scientist, the microbiologist, or there may be something more sinister.”

[52:44-53:06] Wayne Madsen: “Well I think what we have here is a situation with bioethics. They talk a good game in the research – medical research community about bioethics, but it doesn’t seem like there’s any method to enforce the ethics. And if, in fact, this was developed to make money for a certain bio-pharmaceutical companies, of course this is a case of bioterrorism.”

Deep corruption involves everything from contamination of vaccines, to attempts to vaccinate 6 billion people, to assassination of officials who refuse to follow the narrative

[57:25-57:52] Jane Bürgermeister “The vaccine gave her narcolepsy; a brain disorder associated with uncontrollable sleep attacks, hallucinations, and catalepsy. “I trusted them.” she said. “I trusted them. One injection and my whole life changed.”

50,000 people in Germany now have narcolepsy, according to a report in the Welt from January of this year. Every 6th sufferer is a child; the average age is between 15 and 25 years old. The governments of Norway, Sweden, Finland and Ireland have confirmed that the many cases of narcolepsy are due to the pandemic vaccine.”

[59:25-1:00:06] “Baxter nearly started a global pandemic in 2009 when staff contaminated 72 kilos of the seasonal flu vaccine material with a deadly bird flu virus, at its bio-security level 3 facilities in Austria. Baxter had also pre-negotiated contracts to sell the pandemic vaccine.

It has since emerged that Baxter is a site which is critical to U.S. security, according to leaked diplomatic cables published by wikileaks. The question is, who runs this bio-security facility? Is it the CIA? Is it a secret bioweapons lab? How could an instance as sudden as the kind that occurred in 2009 happen at Baxter’s facility?”

[1:00:36-1:00:44] “In 2009, plans to vaccinate 6 billion people around the world were activated by W.H.O. Yes. 6 billion people.”

[1:02:59-1:03:55] “In Poland, no one took the vaccine. Because the health minister, Ewa Kopacz, a doctor, decided that it wasn’t safe enough. “As a doctor, my guiding principle has to be not to damage others.” Kopacz told Polish parliament in 2009. “We will not buy the vaccine against the swine flu.” The Polish health minister was alone in refusing to trigger the pandemic vaccine contract with big pharma. Apart from Russia, a country which also doesn’t have chemtrails. And the Polish government paid a terrible price.

Just days after Ewa Kopacz gave evidence about the pandemic vaccine at the Parliamentary Assembly of the Council of Europe, PACE, 96 top Polish government and military officials were killed in a mysterious plane crash in Smolensk. Itself now the subject of inquiry after enormous amount of evidence showed that this was not an accident. But an assassination attempt.”

Stage is now set

[1:06:06-1:06:45] Jane Bürgermeister: “The stage is now set for another event to trigger a pandemic. This time an act of bio-terrorism could be used, and spark yet another fake pandemic, and push for global mass vaccination campaign. This time, W.H.O. laboratories controlled by big pharma would hype the virus even more than they did in 2009. 

There are more and more signs of the global elite are planning a pandemic scare soon. Big pharma companies have got greater control over the W.H.O.’s pandemic early virus warning system. Allowing them great opportunities for virus/pandemic hype.”

Thank you to the Do You See What I See Productions odysee channel for collecting this footage and compiling it into this video. It is an incredible flashback of the very same attempts that the pharmaceutical industries, media, health organizations, and government have engaged in, in order to enforce vaccines onto the whole world.

And thank you to all of the whistleblowers and reporters who were/are a part of trying to expose these crimes against humanity. Although we are once again repeating history and undergoing these same attempts from the same industries, it is my hope that more and more people become aware of these corrupt organizations and refuse to participate; and instead have courage and integrity and stand up for humanity’s rights and freedom.

Thank you for reading. God bless.

Pfizer-BioNTech/COMIRNATY Vaccine Is Still Under “STUDY” Runs to be Completed at Different Intervals Between 2022-2026

” – known serious risks of myocarditis and pericarditis”

In addition to the many debates and conflicts surrounding the “approval” of the Pfizer/BioNTech/Comirnaty vaccine, there is interesting information to glean from the documents involved surrounding this controversy.

The below documents, some from the FDA’s own website, sheds further light into what seems to be a product still in its experimental/study phase. Some of the revelations are chilling, and doesn’t quite give the reassurance that an “approved” drug of this magnitude is more beneficial to us than what it is purported to be saving us from.

Screenshot of the FDA NEWS RELEASE: FDA Approves First COVID-19 Vaccine
taken on August 31, 2021
[ https://www.fda.gov/news-events/press-announcements/fda-approves-first-covid-19-vaccine ]
Content current as of August 23, 2021

Selected quotes in gray text boxes are from the above document:

“Specifically, in the FDA’s review for approval, the agency analyzed effectiveness data from approximately 20,000 vaccine and 20,000 placebo recipients ages 16 and older who did not have evidence of the COVID-19 virus infection within a week of receiving the second dose. The safety of Comirnaty was evaluated in approximately 22,000 people who received the vaccine and 22,000 people who received a placebo 16 years of age and older.

Based on results from the clinical trial, the vaccine was 91% effective in preventing COVID-19 disease.

More than half of the clinical trial participants were followed for safety outcomes for at least four months after the second dose. Overall, approximately 12,000 recipients have been followed for at least 6 months.

The most commonly reported side effects by those clinical trial participants who received Comirnaty were pain, redness and swelling at the injection site, fatigue, headache, muscle or joint pain, chills, and fever. The vaccine is effective in preventing COVID-19 and potentially serious outcomes including hospitalization and death.”

There are a couple of notes to take away from this document. In the above quote, it doesn’t quite specify how long the clinical trial lasted. Only that more than half of the clinical trial participants were followed for safety outcomes for 4 months after the second dose. It also states that 12,000 of the recipients were followed for at least 6 months.

Both of these numbers (4 and 6) are incredibly low quantities when taking into account pregnant women who are at the beginning of their pregnancy. The length of the clinical trial does not take into account the full 9 months needed to determine a healthy pregnancy, nor does it allow for any time to safely assess the development of the baby once born.

The data in this document also does not include differences between those of the placebo group compared to that of the “vaccine” group. In addition, if we are to only take the 12,000 participants into account, which from the wording of the document seems to allude that these are the recipients of the vaccine, that would still leave 10,000 participants unaccounted for. Just from the amount of vaccine recipients (22,000), this is 45% of their study that the data does not reflect. If we are to include the 22,000 of the participants who received the placebo, the data that was not tracked would rise to 72%.

There is also the challenge of how they determined that the vaccine actually prevented COVID. Were these recipients exposed to someone with COVID or were deliberately inoculated with the disease to see if they would get infected? Many people, myself included, have gone on for more than a year without developing COVID, or at least “COVID symptoms”. Since this data only involved a 4-6 month trial period, how many of us (vaccinated, placebo, or otherwise) can say that we have not contracted COVID during this time-frame either? Is this implying that unless you’re vaccinated, you will most likely get COVID every 4-6 months?

Another consideration to take into account are the many testimonies from well-respected and renowned doctors/scientists/virologists who are adamant in their assessment that these vaccines are unnecessary and instead further harms the immune system rather than help it.

In the same regard, those who are unvaccinated will obviously then not contract any of the possible side effects that are listed in this document as well as the many adverse events that are reported to VAERS. Which leaves one to wonder if the benefits really outweigh the risks of the COVID vaccines.

There is also the slight alteration on a different page of the FDA website that gives further clarification as to the efficacy of the COVID vaccines – which does not reflect that of what many people are influenced to believe:

Under the heading:

Q: What safety information did FDA evaluate to authorize the Pfizer-BioNTech COVID-19 Vaccine for emergency use and approve Comirnaty?

Screenshot of the Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions
taken on August 31, 2021
[ https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/pfizer-biontech-covid-19-vaccine-frequently-asked-questions ]
Content Current as of August 23, 2021

UPDATE on September 6, 2021: Since the FDA website decided to remove this particular section from their FAQ (as of 9/1/2021), here is a screenshot taken from the web archive showing its existence:

“While the vaccine may not prevent infection, symptoms or transmission of the virus from person to person – “

This seems to be the heart of the matter, and although it continues with, “it is effective in preventing hospitalization and death.” it is in direct conflict with what we were led to believe this whole time. Most of the mainstream media, big tech platforms, health agencies, etc. have insisted that vaccines are needed to stop transmission of the virus and to protect those around us. However, this one simple statement defies everything that people were coerced into believing.

And with the last part of the sentence concluding that it prevents hospitalization and death, which even that is debatable when looking at the scope of the situation, it leaves one to wonder why this would not be an option for people to decide to take that risk on their own account. When comparing data of young individuals as well and their extremely low risk of hospitalization and death in the COVID setting, there ARE acknowledged threats when they are injected with the vaccine.

“Additionally, the FDA conducted a rigorous evaluation of the post-authorization safety surveillance data pertaining to myocarditis and pericarditis following administration of the Pfizer-BioNTech COVID-19 Vaccine and has determined that the data demonstrate increased risks, particularly within the seven days following the second dose. The observed risk is higher among males under 40 years of age compared to females and older males. The observed risk is highest in males 12 through 17 years of age. Available data from short-term follow-up suggest that most individuals have had resolution of symptoms. However, some individuals required intensive care support. Information is not yet available about potential long-term health outcomes. The Comirnaty Prescribing Information includes a warning about these risks.”

The FDA is also acknowledging that there are higher risks involved with the Pfizer-BioNTech COVID-19 vaccine and myocarditis and pericarditis, especially in males aged 12-17, and up to age 40.

“Information is not yet available about potential long-term health outcomes.”

“In addition, the FDA is requiring the company to conduct postmarketing studies to further assess the risks of myocarditis and pericarditis following vaccination with Comirnaty. These studies will include an evaluation of long-term outcomes among individuals who develop myocarditis following vaccination with Comirnaty. In addition, although not FDA requirements, the company has committed to additional post-marketing safety studies, including conducting a pregnancy registry study to evaluate pregnancy and infant outcomes after receipt of Comirnaty during pregnancy.”

The document is also stating that the possibility of myocarditis and pericarditis is an accepted issue and will continue to be monitored after the marketing of the Comirnaty vaccine.

And in a rather blunt admission, FDA states on their own website that Comirnaty is not required to evaluate pregnancy and infant outcomes after receipt of Comirnaty during pregnancy. This would explain why the initial trial run was only monitored for 4-6 months. An outline in the BLA (Biologics License Approval) also states that Comirnaty will conduct studies on this group as we see in a later section.

BLA documents state Comirnaty vaccine studies to be conducted for the next several years

Screenshot taken from from the FDA BLA Approval on August 31, 2021
[ https://www.fda.gov/media/151710/download ]
Document dated August 23, 2021

Text below is page 5 of the FDA BLA Approval document

Your deferred pediatric studies required under section 505B(a) of the Federal Food,
Drug, and Cosmetic Act (FDCA) are required postmarketing studies. The status of
these postmarketing studies must be reported according to 21 CFR 601.28 and section
505B(a)(4)(C) of the FDCA. In addition, section 506B of the FDCA and 21 CFR 601.70
require you to report annually on the status of any postmarketing commitments or
required studies or clinical trials.

Label your annual report as an “Annual Status Report of Postmarketing Study
Requirement/Commitments”
and submit it to the FDA each year within 60 calendar
days of the anniversary date of this letter until all Requirements and Commitments
subject to the reporting requirements under section 506B of the FDCA are released or
fulfilled. These required studies are listed below:

1. Deferred pediatric Study C4591001 to evaluate the safety and effectiveness of
COMIRNATY in children 12 years through 15 years of age.

Final Protocol Submission: October 7, 2020

Study Completion: May 31, 2023

Final Report Submission: October 31, 2023

2. Deferred pediatric Study C4591007 to evaluate the safety and effectiveness of
COMIRNATY in infants and children 6 months to <12 years of age.

Final Protocol Submission: February 8, 2021

Study Completion: November 30, 2023

Final Report Submission: May 31, 2024

3. Deferred pediatric Study C4591023 to evaluate the safety and effectiveness of
COMIRNATY in infants <6 months of age.

Final Protocol Submission: January 31, 2022

Study Completion: July 31, 2024

Final Report Submission: October 31, 2024

Submit the protocols to your IND 19736, with a cross-reference letter to this BLA STN
BL 125742 explaining that these protocols were submitted to the IND. Please refer to
the PMR sequential number for each study/clinical trial and the submission number as
shown in this letter.

Submit final study reports to this BLA STN BL 125742. In order for your PREA PMRs to
be considered fulfilled, you must submit and receive approval of an efficacy or a labeling supplement. For administrative purposes, all submissions related to these required
pediatric postmarketing studies must be clearly designated as:

• Required Pediatric Assessment(s)

As the document states, the completion study of Comirnaty postmarketing (after approval) is not due until May 31, 2023 / Novermber 20, 2023 / July 31, 2024 respective of older to lower age groups. There is also another important acronym to consider, which is the IND, which stands for Investigational New Drug.

With this knowledge in hand, it’s important to note that the clinical trial run was monitored for 4-6 months after the second dose on around 55% of the recipients, while the actual “approved” drug still in its investigational/study stages is set to be monitored for 2-3 years. This is a sizeable difference in the amount of time to determine safety and efficacy, especially when considering the many events already reported to VAERS. And according to the Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions page from the FDA website:

Screenshot taken from the FDA Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions
on August 31, 2021
[ https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/pfizer-biontech-covid-19-vaccine-frequently-asked-questions ]
Content current as of August 23, 2021

Q: Are vaccine providers required to report side effects?
A: Providers administering Comirnaty or Pfizer-BioNTech COVID-19 Vaccine must report to the Vaccine Adverse Event Reporting System (VAERS) and to Pfizer the following information associated with the vaccine of which they become aware:
  • Vaccine administration errors whether or not associated with an adverse event
  • Serious adverse events (irrespective of attribution to vaccination)
  • Cases of Multisystem Inflammatory Syndrome
  • Cases of COVID-19 that result in hospitalization or death

Acknowledged myocarditis and pericarditis issues being studied on children

” – known serious risks of myocarditis and pericarditis”

Screenshot taken from from the FDA BLA Approval on August 31, 2021
[ https://www.fda.gov/media/151710/download ]
Document dated August 23, 2021

Text in the gray box below are from pages 6-8 of the FDA BLA Approval documents
[ https://www.fda.gov/media/151710/download ]

We have determined that an analysis of spontaneous postmarketing adverse events
reported under section 505(k)(1) of the FDCA will not be sufficient to assess known
serious risks of myocarditis and pericarditis and identify an unexpected serious risk of
subclinical myocarditis.

Furthermore, the pharmacovigilance system that FDA is required to maintain under
section 505(k)(3) of the FDCA is not sufficient to assess these serious risks.

Therefore, based on appropriate scientific data, we have determined that you are
required to conduct the following studies:

4. Study C4591009, entitled “A Non-Interventional Post-Approval Safety Study of
the Pfizer-BioNTech COVID-19 mRNA Vaccine in the United States,” to evaluate
the occurrence of myocarditis and pericarditis following administration of
COMIRNATY.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: August 31, 2021

Monitoring Report Submission: October 31, 2022

Interim Report Submission: October 31, 2023

Study Completion: June 30, 2025

Final Report Submission: October 31, 2025

5. Study C4591021, entitled “Post Conditional Approval Active Surveillance Study
Among Individuals in Europe Receiving the Pfizer-BioNTech Coronavirus Disease 2019 (COVID-19) Vaccine,” to evaluate the occurrence of myocarditis
and pericarditis following administration of COMIRNATY.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: August 11, 2021

Progress Report Submission: September 30, 2021

Interim Report 1 Submission: March 31, 2022

Interim Report 2 Submission: September 30, 2022

Interim Report 3 Submission: March 31, 2023

Interim Report 4 Submission: September 30, 2023

Interim Report 5 Submission: March 31, 2024

Study Completion: March 31, 2024

Final Report Submission: September 30, 2024

6. Study C4591021 substudy to describe the natural history of myocarditis and
pericarditis following administration of COMIRNATY.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: January 31, 2022

Study Completion: March 31, 2024

Final Report Submission: September 30, 2024

7. Study C4591036, a prospective cohort study with at least 5 years of follow-up for
potential long-term sequelae of myocarditis after vaccination (in collaboration
with Pediatric Heart Network).

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: November 30, 2021

Study Completion: December 31, 2026

Final Report Submission: May 31, 2027

8. Study C4591007 substudy to prospectively assess the incidence of subclinical
myocarditis following administration of the second dose of COMIRNATY in a
subset of participants 5 through 15 years of age.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this assessment according to the following schedule:

Final Protocol Submission: September 30, 2021

Study Completion: November 30, 2023

Final Report Submission: May 31, 2024

9. Study C4591031 substudy to prospectively assess the incidence of subclinical
myocarditis following administration of a third dose of COMIRNATY in a subset of
participants 16 to 30 years of age.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: November 30, 2021

Study Completion: June 30, 2022

Final Report Submission: December 31, 2022

It is interesting that the timing to be considered for approval of these vaccines was only a 4-6 month timeframe, however, known dangers/risks, identified as “serious”, are still allowed to be approved and to be studied for 2+ years.

The document also recognizes that myocarditis and pericarditis is enough of a concern to happen after administration of the Comirnaty vaccine, since it mentions several studies just for this specific adverse event, and to continue to assess these reports.

In addition to all of the substudies to be conducted, there is a study to be initiated on a select group of participants to administer a third dose of the Comirnaty vaccine.

All of this information leads credence to the fact that even though the Comirnaty vaccine has “officially been approved” by the FDA, it is still in the investigational stages and being experimented upon on the public. And it goes without saying, but if myocarditis and pericarditis (on top of other reported side effects) are serious risks especially in children (“The observed risk is highest in males 12 through 17 years of age.”), then for this known risk to be offered to infants/toddlers defies any ethically moral boundaries and is in direct violations of the Nuremberg Code.

The next section also provides further evidence that there have been NO studies in the safety/efficacy of the Pfizer-BioNTech/Comirnaty vaccine on pregnant women.

Pregnancy/Births were not studied during the initial Pfizer-BioNTech/Comirnaty trial runs

Another snippet from the FDA Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions website page, states the following:

Screenshot taken from the FDA Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions
on August 31, 2021
[ https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/pfizer-biontech-covid-19-vaccine-frequently-asked-questions ]
Content current as of August 23, 2021

Q: Can pregnant or breastfeeding women receive the Comirnaty or Pfizer-BioNTech COVID-19 Vaccine?

A: While there have been no specific studies in these groups, there is no contraindication to receipt of the vaccine for pregnant or breastfeeding women. Pregnant or breastfeeding women should discuss potential benefits and risks of vaccination with their healthcare provider.

The acknowledgement above seems to indicate that the FDA and Pfizer-BioNTech/Comirnaty company have side-stepped this particular group in their vaccine studies, and have left it up to the healthcare provider to determine whether or not to administer this vaccine to pregnant women or women who are breastfeeding. This alone should be enough of a statement that there is no sufficient/professional data to analyze if the Comirnaty is safe during pregnancies/breastfeeding stages.

And if one were to consider the VAERS reporting system, in which the Pfizer-BioNTech company is required to report to, there have been numerous conditions of miscarriages/stillbirths/complications during pregnancy after administration of the COVID vaccine. While it is difficult to determine if these complications were a direct result of the vaccine, it is up to the scientific/healthcare community to investigate these cases in a thorough, unbiased and uninfluenced manner.

Another extremely alarming section of the FDA BLA Approval documents shows the following trial to be monitored in pregnant women:

Screenshot taken from from the FDA BLA Approval on August 31, 2021
[ https://www.fda.gov/media/151710/download ]
Document dated August 23, 2021

Text in the gray box below are from pages 9-10 of the FDA BLA Approval documents
[ https://www.fda.gov/media/151710/download ]
POSTMARKETING COMMITMENTS SUBJECT TO REPORTING REQUIREMENTS
UNDER SECTION 506B

We acknowledge your written commitments as described in your letter of August 21, 2021 as outlined below:

10. Study C4591022, entitled “Pfizer-BioNTech COVID-19 Vaccine Exposure during
Pregnancy: A Non-Interventional Post-Approval Safety Study of Pregnancy and
Infant Outcomes in the Organization of Teratology Information Specialists
(OTIS)/MotherToBaby Pregnancy Registry.”

Final Protocol Submission: July 1, 2021

Study Completion: June 30, 2025

Final Report Submission: December 31, 2025

There are a couple of key takeaways in this section that are of incredible importance. One major term to focus on is the word “NON-INTERVENTIONAL“.

According to What is a Non Interventional Study?, “In general, a non interventional study (NIS) (also called a non interventional trial) is where a patient takes regular medicine, prescribed according to the label. In an NIS, the researcher sets out to exert as little influence as possible on the patient’s condition while studying a medicine’s “…effectiveness, safety and tolerability under real life conditions” (Mishra & Vora, 2010).”

The article also reiterates multiple times that “non-interventional” studies are observational studies – the researchers are not to interfere with the dosages in any way but to prescribe them exactly as listed on the label. It also seems to imply that even if severe side effects show up, they are to still carry through with the “medicinal product” in that patient as prescribed. Another insinuation that one can make is that in order to not interfere with the study, it is not recommended to prescribe treatments that may help alleviate potential side effects. The term “tolerability” is implying to keep the patient going through the side effects in order to continue to study the long-term effects of the investigational new drug.

However, with the inclusion of “real life conditions”, it doesn’t indicate whether the patient can seek out physicians to investigate what is causing the side effects in their system and engage in therapeutic treatments to alleviate these effects. If a study is to be conducted in real life conditions, then it is to be expected that patients will seek treatments on their own while the researcher is only required to observe the patient to see how the alternative treatments interact with the drug/symptoms.

The same article goes on to state that the UK/EU have different definitions of what “non-interventional” means. “Aronson (2004) states… “the term ‘non-interventional’ in the Directive doesn’t mean non-interventional (i.e. non-interference) at all; it refers to an intervention with a licensed medicinal product.”

There is controversy and conflicts in this statement as another article, Interventional or Non-Interventional? Analyzing the Differences Between Clinical Studies Using Medicines in the European Union points out:

“Although defined in DIR 2001/20/EC, non-interventional studies are outside its scope. Due to the lack of harmonized regulation, some studies designed to be non‑interventional may be considered clinical trials by EU authorities. The two blinded studies described in Table 4 (see PDF) were considered clinical trials in the EU for planning on collection of data to support the marketing authorization application of experimental IMPs, despite no IMP being given and normal clinical practice being kept during the study period. Sponsors are thus advised to consult with authorities when planning studies under these conditions and/or whenever the objectives or design may raise questions.”

Further in the article, it states the following, which again, is not reassuring considering the policies/guidelines/mandates that authorities have been engaging in in order to mandate these investigational new drugs (COVID vaccines) onto the public:

“There is no centralized submission procedure for non-interventional studies with the exception of non-interventional PASSs, imposed as an obligation by an EU competent authority.{9} Because non-interventional studies do not have harmonized legislation, some Member States require submissions to regulatory authorities, while others do not. It is therefore important that sponsors are familiar with the regulatory framework of target EU Member States, and that they consult with local competent authorities and ethics committees (ECs) when justified.”

It’s sad to have to point this out, but the quote does specify “competent” authorities. And even the inclusion of “ethics committees” is not comforting seeing as how one of the leading figures in ethics study is Christine Grady, Chief of the Department of Bioethics at the National Institutes of Health Clinical Center, and wife of Anthony Fauci – Director of the National Institute of Allergy and Infectious Diseases and Chief Medical Advisor to the president, and who is also a large spokesperson for the experimental injections.

The other takeaway from section 10 of the FDA BLA documents is the term “TERATOLOGY“.

Definition of teratology
: the study of malformations or serious deviations from the normal type in developing organisms
merriam-webster/teratology

Teratology, branch of the biological sciences dealing with the causes, development, description, and classification of congenital malformations in plants and animals and with the experimental production, in some instances, of these malformations. Congenital malformations arise from interruption in the early development of the organism. Malformations in human infants, for example, may occur because the infant’s genotype contains mutant genes or includes an abnormal number of chromosomes; they also may occur if early in pregnancy the mother has had German measles (rubella), has taken some injurious drug, or has been exposed to an injurious dosage of radiation. Experimental studies suggest similar types of factors can cause malformations in animals and plants.”
britannica/teratology

Now when you combine the terms “non-interventional” and “teratology” together, it is suggesting that the ongoing studies (that were not conducted to begin with even in a clinical trial setting, as per the FDA’s own response) on pregnant women with Comirnaty and on the developing baby, will be monitored with as little intervention as possible and is mostly to be observed for malformations/genetic defects/miscarriages/etc.

In other words, safety and efficacy were never studied in this particular group, and neither was it studied in infants. It has also not been studied for long-term analysis, as the 4-6 month trial runs proves. The current “approval” it is undergoing now is an authorized experiment on the human population that is posing incredibly unnecessary risks when considering the many effective treatments that are already available to combat respiratory illnesses. And the insistent assertiveness to push this “investigational new drug” onto babies/children who are at extremely low risk for this illness is a disastrous decision from those in an “authoritative” position and should be investigated for malfeasance and misconduct.

This is also not the first time that government agencies/health industries/etc. have conducted experiments on the public.

The Tuskegee/Syphilis experiment was initiated onto a selection of African American men between 1932-1972. The study was only stopped (allegedly) after a publication was released on Associated Press in 1972 about the immorally unethical experiments being conducted on this group:

“Of about 600 Alabama black men who originally took part in the study, 200 or so were allowed to suffer the disease and its side effects without treatment, even after penicillin was discovered as a cure for syphilis. Treatment then probably could have saved or helped many of the experiment participants, PHS officials say.”AP WAS THERE: Black men untreated in Tuskegee Syphilis Study

This study seems to echo the sentiments we see going on with the coronavirus situation, in which only one type of drug is being promoted (the COVID vaccines) while suppression of other treatments that have been proven to work (such as Ivermectin) has been denounced by the very same government/health/medical fields that have conducted these experimental studies.

A study that involved the CDC/FDA’s approval, this time on Black and Latino babies, was conducted in the early 1990’s and involved the measles vaccine:

“1990: CDC Inoculated Black and Latino Babies with an Unlicensed Measles Vaccine
A covert clinical trial by the Center for Disease Control (CDC) and Kaiser Permanente inoculated Black and Latino babies with an experimental measles vaccine without informing parents the vaccine was experimental. More than 1500 six-month old black and Hispanic babies in Los Angeles are given the deadly “experimental” measles vaccine that had never been licensed for use in the United States; a vaccine that had been tested in African and Mexican babies resulting in high death rates. The parents were never informed and they never gave their consent. The CDC harmed babies, violated federal law, and trampled on parental rights with impunity.”
1990 FDA Issued a Waiver From Consent; Covert CDC Experimental Vaccine Test on Black / Latino Babies

It’s interesting that the measles vaccine experiment identifies Kaiser Permanente specifically, because as we see in another section of the FDA BLA Approval for Comirnaty, it seems as if Kaiser Permanente makes another appearance in the role of human experimentation:

Text in the gray box below is from page 10 of the FDA BLA Approval documents
[ https://www.fda.gov/media/151710/download ]

13. Study C4591014, entitled “Pfizer-BioNTech COVID-19 BNT162b2 Vaccine
Effectiveness Study – Kaiser Permanente Southern California.”

Final Protocol Submission: March 22, 2021

Study Completion: December 31, 2022

Final Report Submission: June 30, 2023

It would seem that the approval by the FDA of these IND drugs (Pfizer-BioNTech/Comirnaty vaccine) is a way for the government/health agencies to skirt away from liability by stating that since the vaccines are no longer “experimental” by their definition, and that they are FDA “approved”, it is no longer required to gain informed consent of these drugs. In addition, as to the technicality of their terms and protocols, there are a multitude of ways to interpret their “informed consent” rules, which officials can then bend or define in any way that best reflects the use of their study/drug.

[ https://www.fda.gov/regulatory-information/search-fda-guidance-documents/informed-consent#exceptions ]

Also keeping in mind how long it was determined before the “health agencies” granted approval of the Pfizer-BioNTech/Comirnaty vaccine – (4-6 months) – it would be conclusive to state that the vaccines have NOT sufficiently been studied in young children or pregnant women (or even the rest of the age groups because of the short amount of time the clinical trial study was conducted in), and the subsequent approval of this vaccine is to continue this research on the population who is exceedingly being pressured into taking this investigational new drug.

There is also the matter of the many adverse events that have been reported since the inoculation of these injections, that have largely gone unheeded within the health/medical institutions that are endorsing this drug. Other than the widely acknowledged myocarditis and pericarditis, most common in young males, which is still being studied and allowed to persist onto the public.

So again, taking into account the collusion of the government/health/medical/research fields to conduct experiments on the public, it would be necessary to reflect upon these agencies for additional breaches upon human rights, consent, and ethical behavior.

Fair use disclaimer: Some of the links from this article are provided from different sources/sites to give the reader extra information and cite the sources, but does not necessarily mean that I endorse the contents of the site itself. Additionally, I have tried to provide links to the contents that I used from other sites as an educational and/or entertainment means only; if you feel that any information deserves further citation or request to be clarified, please let me know through the contact page.

Featured image by Ahmad Ardity from Pixabay

Dr. Richard Fleming Interview with Mike Adams | “The Vaccines ARE the Bioweapon” [Full Transcript]

“This is a violation of science. This is a violation of medicine. This is a violation of humanity.”

In keeping with providing written transcripts for those who prefer to read text as opposed to watching videos, I have transcribed the following interview between Mike Adams and Dr. Richard Fleming.

Another in-depth/informative video that Mike Adams conducted, this time with Dr. Peter McCullough, that is transcribed in full can be found here:
Dr. Peter McCullough Interview with Mike Adams | “All to prepare the population for mass vaccination.” [Transcript]

Thank you to Mike Adams and Dr. Richard Fleming. While all of the information is incredibly helpful and insightful, I did provide some embellishments to highlight exceptionally pertinent topics.

 

Also thank you to all the doctors/scientists/researchers, etc. who have been brave enough to stand up for their patients and for humanity in general. Your bravery and integrity speaks volumes of your character and exemplifies what it means to be a strong, compassionate individual, especially in the midst of adversity and vitriol.

Mike Adams @00:33: “Welcome to BrighteonConversations, I’m Mike Adams, the founder and host of brighteon.com, today. 

We have a special guest, first-time guest. A brilliant individual who’s an author of a book called “Is COVID-19 a Bioweapon?” His name is Dr. Richard Fleming, his website is flemingmethod.com, and he is not only trained as a physicist and a nuclear cardiologist, but, of course he’s an author and researcher and doctor – we’re going to talk to him, ask him lots of questions about what’s going on with COVID today.

So thank you for joining me. It’s an honor to have you on, welcome to BrighteonConversations.”

Dr. Richard Fleming @1:07: “It’s my pleasure to be here, thank you for the invitation.”

Mike Adams: “Well absolutely.

It’s fascinating, just really fascinating to be able to hear from people like you. Let’s start with some basics. Your book asks the question, ‘is the COVID-19 a bioweapon?’ And there’s a lot behind that, but, what’s the short answer? And what else does the book provide to support that?”

Dr. Richard Fleming @1:30: “Well there’s – ahem, the short answer, um, I think… I’m going to leave to the readers, for them to decide. I think, uh… a year ago, that question would have been heresy, and, you know, even though I was asking it a year ago, but it’s amazing how just as information comes out, people become much more aware of reality.

This book really lays out in detail a lot of information with people. It tells you to begin with what ‘gain of function’ is. Which is what the topic of the day is. The ability of scientists to take infections like a virus and make them more infective or potentially more dangerous. But it also, it provides a lot of information sequentially so you can understand where the moneys came from to build this virus, who published research – just literally published the research over the, you know, two to three decades, showing a nice paper trail of data, who got the patents on it, whose names are connected, how the funding got connected with it; and then, you know, really addressing that spike protein which is the actual bioweapon itself.

You know, the gain of function, man-made, altered, critical component to this virus being so infectious and dangerous – um, and amazingly enough that in and of itself explains to you why the drug vaccine biologics aren’t working at this point in time. Which we can get into if we have time. And then just an explanation also about the intentional release of this, of this virus, and recognition that this is not the first one of these viruses. It’s kind of a version number 2. And even though there’s a number of coronaviruses, which means viruses that look like a crown when you look at them under an electron microscope, this one is the 7th one that has been identified to infect in people, and it’s the 2nd one that holds the name of ‘severe acute respiratory syndrome coronavirus’. And it’s number 2 because number 1 was from 2002, also delivered to the world out of China. And by very much the same people.”

Mike Adams @3:52: “That leads me to a recent video by Dr. David Martin that I’d like your comment on. And I just happen to have these notes in front of me here. He was referring to a patent: April 19th 2002, U.S. patent, 7279327 – in which it appears that U.S. scientists created SARS. The – one of the early renditions of SARS, which later on was altered, was transformed to become SARS-CoV-2, eventually. But as you just said, some of these patents go back 22 years, and the research goes back even before that.

It appears that, like you said, there’s a long paper trail that they have been funding these efforts and deliberately working to engineer these viral – I don’t know – nanoparticles, pathogens, for some reason. But what about the motivation, then? Do you get into that in your book? What’s the – why are they doing this? Why?”

Dr. Richard Fleming @4:54: “Right, well, I think to understand the motivation of the people involved, you have to understand who’s involved. And when you look at, as explained in the book, where the funding from the United States came from. You know, more than 60 million dollars, which may not sound like much when we’re talking about throwing a trillion out here, and a trillion out there, I mean, 60 million dollars is still a fair amount of money for research scientists to work with; particularly when you consider over three decades, that amount of money was substantial.

And you simply asked, where did that money come from? Well it came from National Institutes of Health. It came from the National Institute of Allergy and Infectious Diseases. It came from the Department of Defense. In fact, more than half of it came from the Department of Defense, along with, as you’ll see in the book, a David Franz, who was a former deputy commander at Fort Detrick.

And in case anybody wants to take the argument that, ‘wait a minute, Fort Detrick is the U.S. military base, it doesn’t have anything to do with viruses and NIAID’, I would point out to you that I have received several emails from people trying to recruit me as a physicist for imaging at Fort Detrick, of viruses funded by NIAID. So I actually have documents of my own that have been sent to me, trying to recruit me, [Mike Adams laughs: “That’s great.”] to be involved in this, in this work. So, I think probably not anybody else has that. Um, you need to be a physicist to get that type of query from them. So clearly they are involved.

And then you asked the question, ‘what do these agencies work with?’ Well, as I frequently tell people, the DOD is not involved with the girlscouts. They don’t sell thin mints and they don’t help boyscouts sell popcorn. Um, they do other things. And what that really means is when you get right down to it, is that if you build a biologic – like this virus – which has no beneficial effect or benefit for mankind, which it clearly doesn’t, then you have violated the biologic weapons convention treaty. [Mike Adams: “Good point.”] And you are now, you are now an international criminal.”

Mike Adams @7:08 “Now, we spoke with doctor Francis Boyle on that issue, he’s an expert in that area, but from what you’re saying, I’m asking you to confirm this, if it is so, that it seems like the United States military was attempting to offshore the research in order to circumvent limitations on such research in the United States. So they funneled money through EcoHealth Alliance and Peter Daszak and so on, to the Wuhan Institute of Virology and then partnered essentially with the People’s Liberation Army, controlling the Wuhan Institute. 

So now you have the military of the United States and the military of China conducting research in China on biological weapons, which is obviously that intellectual property would be shared with both nations. Is that an accurate statement, or am I wrong in any point there?”

Dr. Richard Fleming @7:54: “No, that’s – that’s pretty good. I mean, the federal fundings in the United States, much of it, although not all of it, got circumvented through Peter Daszak at EcoHealth. He paid moneys off to Ralph Baric at the University of North Carolina, but that’s not the only American Institution, and to Shi Zheng-li at the Wuhan Institute of Virology. And we’ve seen decades of them working back and forth.

In fact, there’s some data that I have that isn’t yet in the book, and I’m saving it for a special purpose, um, and I’ll let your readers think about what that special purpose might be, showing that these same people also worked genetically to alter viruses so that they would escape the ability of our immune system to fight them off. And they successfully proved this. So this particular virus doesn’t have that aspect to it, but clearly if you’re developing one biological weapon, you know research scientists like myself don’t work on a project and go, ‘Well, that’s good. We’re going home now for the rest of our lives.’ I mean, you’re constantly working on new things. And one of the ways to think about this is the United States is playing China, China was playing the United States, and look who got caught in the crossfire.”

Mike Adams @9:07 “And the institution of this twisted science was playing us all, because my next question to you is about – remember when Peter Daszak authored that article, I think it was published in the Lancet, that initially proclaimed: “Oh, this is zoonotic. This couldn’t possibly have come from a lab.” I mean they were very insistent and they were arm-twisting and they were recruiting. And some of this came out in the FOIA request of Fauci’s emails where Daszak and Fauci were coordinating this, this fairy tale, to try to proclaim this wasn’t built in a lab. What are your comments on that?”

Dr. Richard Fleming @9:42: “Well, I have a very personal comment. You know, a lot of people spend their lives as research scientist, trying to become reviewers and editors for major league journals; it’s a big plus for us. I resigned in 2020 from two journals: The British Medical Journal Open Quality, and the Lancet. And I did that because of this type of use of a journal that used to be prestigious, to represent science at its best, being used as a manipulative tool for somebody to drive their agenda. And that unfortunately was the prostitution of our research journals.”

Mike Adams @10:22 “Wow. Wow! So, you said something to me related to this before we started our interview, that Fauci does not represent science. And, this is my next question, cause I’m very concerned about that. I mean, my background, I’m a food scientist. I run a mass spec food science lab. And we do very accurate quantitation and method development for glyphosate concentration and things like that for our business. That’s what we do. We test everything. Right? So we’ve very practical application. And I have always believed in the tenets of science. You know, let’s develop a method, let’s calibrate the instrument, let’s run it, let’s compare it to certified reference materials, do all these things. Yeah, that’s valid. That’s legit. And yet I see the institution of science committing suicide! Apparently. Committing suicide – credibility suicide. What do you think?”

Dr. Richard Fleming @11:13: “Right. Well I think part of the, part of the problem is because somebody calls themselves “scientist” doesn’t mean that they were actually practicing science. I mean, it’s more of a pseudoscience when you get into that. I was in medical college at the time that HIV hit. You know? And we got to see it first-hand. And I am hard-pressed, and that was in the early 1980’s, I am hard-pressed to find any substantive quality published research since that time that has Anthony Fauci’s name to it. So… you may be in charge of an agency, but that doesn’t mean that you’ve contributed to the field of science. Science builds upon all the work that, just as you said, you have to – you have to figure out what you’re doing, research-wise, you have to figure out how you’re going to answer that question, you have to be able to make your equipment work.

A good point to stop, at PCR, right there. Equipment working.

Kary Mullis developed the PCR test to look for genetic sequence. That’s what the patent is for. It looks for genetic sequence. If you read that patent, Kary Mullis said you stop at 20 cycles. It gets you a 100% of the genetic material if it’s there; anything else becomes gobbledy-gook, using that good scientific term that my parents taught me a long time ago. And what happened to that scientific tool? Well it got abused. By people who claim that they’re running science, but didn’t really understand the science.

You know, Mullis and I have two things – couple things in common. One, both patents, [owners]. And the second, we both think that Fauci is anything but science and we don’t think he’s much of a scientist. And we’ve both declared that we would love an opportunity to debate with him at any point in time about the science.

And that’s an offer that, you know, I make here again, which is: Anthony Fauci – anytime, anyday, anywhere, any place, you want to have a debate about SARS-CoV-2 and real science, let’s do it, so the American people can see what the truth of this is.

Mike Adams @13:18: “Is he hearing you say that, Dr. Fleming?

This is what gives me hope in the future of science. Because you are obviously an informed, intelligent, analytical person. And this is what desperately needs to be applied right now.

Because just going back to PCR, I’ve heard from other people, cause I’m always interviewing and talking to people, there are individuals out there who would just go to Thermo Fisher, and they would purchase PCR equipment, that they had never been trained on, they’d never run before – and it’s not that expensive, in terms of lab science. For a hundred grand or a hundred and twenty grand, you can get a PCR and a sample prep, you know, instrument. And they would run these things, and they would make a million dollars in one weekend doing tests for a local clinic or a hospital. Cause it’s all being billed out to the government.

And so, this is the case, exactly as you said, it was abused! And they would turn the cycle thresholds up to 35 or more! And they’re just – they’re basically just reporting instrument noise. This is background noise and they call it COVID. Wow!”

Dr. Richard Fleming @14:24: “Yeah, noise to signal ratio is the physics term, and they’ve introduced a bunch of noise into this. You know, what we have demonstrated very clearly in the almost 2 years here is that using PCR tests, we have demonstrated that respiratory viruses are transmitted from person to person, by respiratory pathways. We have proven that the inflammation and blood-clotting that’s associated with COVID-19, that I talked about first in 1994, is the cause of these diseases; that if you don’t treat that, people die.

And we have shown that if you take a drug vaccine, that is directed towards just a part of one type of variant of a species of coronavirus, and you make an immune response to that, you’ll make an immune response, but when you dump billions of that into the body, you’ll make a massive immune response and have very adverse effects, which is what we’re seeing.

It didn’t make any – it didn’t make any difference in the number of people who end up with the COVID or dying; vaccinated versus not. But we managed to devote massive immune responses and then we were able to put pressure on the virus to promote one of the variants, in this case delta – but there’s lambda and a whole series of these that are out there, that if you actually attack one part of, in this case the virus, you’ll promote the spread of the other types that are immune. Because the antibodies are completely different for that type of spike protein.”

Mike Adams @15:57: “Right. Viral, just viral evolution add up to host adaptation.” 

Dr. Richard Fleming: “Yeah, I mean the virus – it’s like antibody resistant bacteria. Those anti – those bacteria are already resistant. But if you dump antibiotics into the system indiscriminately, you’ll kill off the ones that can’t handle that, but the antibody resistant ones will flourish. And that’s all we’ve done. Is we have demonstrated, wow, pressure selection works.

So we know that viruses pass by air, we know that if you don’t treat patients they die, and we know that if you put pressure on a species like this virus, it will select out for the ones that are most viable to live and cause a problem. And like Albert Einstein said, “Insanity is doing the same thing over and over again and expecting a different result.” Well, let me ask everybody: how did our masking, quarantining, deprivation of medical treatment, and pressure selection on a virus work? – Wait a minute. We’re doing the same thing we did 2 years ago. I think that answers the question. 

And, with the book, we now who know who’s paying for it and the people who paid to develop it, are the same people that are blocking the treatments, are the same people getting money for the vaccines; and that should raise just a few eyebrows out there, among the at least 30% of the U.S. population that we know are beginning to listen to the science, as opposed to the pseudoscience political speech.”

Mike Adams @17:29: “My, you raised so many issues here, let me see if I can remember all the questions. Just from that.

So, one thing you’re referring to is the epidemiological effects of the viral adaptation pressures caused by mass vaccinations of people during a strong outbreak. Now, Geert Vanden Bossche, Dr. Bossche, if I’m pronouncing it correctly – Bossche – he’s warned about that exact scenario. And he’s an epidemiologist, a pro-vaccine epidemiologist, or researcher, and it seems now, when you have certain countries like Israel and Australia that are very heavily vaccinated and now they’re starting to see that the severe patients who are experiencing hospitalization, have now sometimes 74% of them have been vaccinated. Is that – seeing that, is that consistent with what you are describing?”

Dr. Richard Fleming @18:23: “Absolutely. And when they talk about the unvaccinated having problems as well, well of course, because it’s all been selected out to produce these slightly more infective delta variants. So yeah, they’ve done a brilliant job of proving science is correct, um, they just haven’t figured out quite how to handle this. And that would require that they step back and go, ‘You know, maybe we should have been more upfront and honest with you about what we were doing with this money and the development of this bioweapon.’

Um, because now, now these people are criminally culpable. They have violated a Biological Weapons Convention treaty. They have violated informed consent with the Declaration of Helsinki. They have violated the International Covenant of Civil Political Rights Treaty. They have violated the Nuremberg Code.

Physicians in the United States that are vaccinating people who have not read the package inserts to obtain the information about the drugs are violating their Hippocratic Oath – but, wait a minute, there’s actually nothing on those package inserts. They say that they are intentionally blank, so had they read them, they would have seen that they were intentionally blank and that they don’t have informed consent to give to the patients.

What we’re seeing from the VAERS is that all the inflammation and blood-clotting that I warned about in 1994 is exactly what we’re seeing in healthy people with this massive immune response, causing heart damage, liver damage, neurologic diseases; all the things that we’ve been warning about. All the things that we have made worse by the very approach that we’ve done to this.

And you know, if we were just human beings and we actually had gotten exposed to a virus that was doing this to us, that would be one thing, and you could say ‘oops, my bad’, you know, using the vernacular. But the problem is, we’re the ones who developed it. And by ‘we’ I don’t mean me. I mean the people that are talked about in this book. The people that, and you’ll see in the book, where they took one part of one virus, combined it with another part of another virus, then inserted separate nuclei type bases in there to make it more infective.

I mean, this is – I don’t know… you know, they might have at one point in time thought they were doing something for mankind decades ago, but when you get to the place that you’ve jumped evolutionary barriers, by decades and tens and hundreds and perhaps thousands of years, and produced something that we would not have to be worrying about, and now you’ve produced this gain of function weapon, in violation of treaties?

First off, you’re criminally accountable, and secondly, anybody who requires mandated vaccines without these informed consents, have violated international treaties. And if you are an elected official, or an appointed official, and you’ve taken an oath to defend and uphold the Constitution of the United States, you have violated that oath. And under that oath and the Constitution, that’s treason.”

Mike Adams @21:36: “So what you are describing, and I think our audience agrees with everything that you’ve just described, but I want to ask you one step further on this.

What you appear to be describing, is a large-scale organized crime, racketeering, money-laundering operation, you know, the government’s laundering money into the hands of big pharma, while big pharma is funding the FDA and funding the politicians and the CDC, which owns patents on some of the earlier coronaviruses. Probably receiving royalties of some kind on all of this. And keep people like Walensky, the director of the CDC, her husband, his company, receive millions of dollars in NIH grant money; approved by Fauci and so on.

This is an incestuous money-laundering racket with the cost being born by the people. Because the vaccine companies have legal immunity from indemnification from lawsuits. But the people then have to bear their own medical cost from the adverse reactions, long-term effects, long-term blood clot, inflammation effects; all of these things. This is – if this is all true, it’s beyond insidious, it’s beyond criminal, it is – it is perhaps the most diabolical attack on humanity that has ever been waged on this planet. Would that be accurate?”

Dr. Richard Fleming @22:56: “Absolutely. When Adolf Hitler started the Nazi regime, the first people that they put in concentration camps were not the Jews. It was the intellectuals. The people that would open debate discussions about what was going on. After he accomplished that, then he went after the Jews and the homeless and anybody else he thought that was undesirables.

So the first thing you do, if you want to have this type of effect, is you take out the intellectuals so that people will not discuss and debate what’s really going on and figure it out. And what happened in Germany? The doctors went along with it, the politicians went along with it, the judges went along with it. The only difference is that they really had a very small group of people that they were experimenting on, compared to what’s going on today, because this is a global experiment. And you’re either part of the experimental, or you’re part of the control group, right now.

You know? And the data is pouring in, whether we like it or not. And history is being written whether we like it or not. So, Adolf Hitler and Josef Mengele are turning over in their graves right now going, ‘wow, we could not have imagined being able to pull anything off on this massive scale’. And yet, we’ve shown repeatedly that if you lockdown people and quarantine them and keep them from talking, and feed them the agenda.

Goebbels – no, Goering, rather, at the Nuremberg Trial in 1947, when he was being held accountable for his crimes against humanity, looked at the prosecutors – the American prosecutors, and said, “If you want to manipulate a people, and have them do what you want as a government, all you have to do is tell them there’s a problem, tell them what the answer to that problem is. Tell them that anybody who opposes that answer is a traitor to the country. And you can get them to do it.”

And the Americans said, “You, you are so wrong. We live in the United States. We elect our officials.” And he laughed at them and he said, “Look. A republic. A parliament. Communist. Socialist. Fascist. It doesn’t matter. People are controlled the same way. You isolate them, you tell them there’s a problem, you tell them what the answer to the problem is, you tell them anybody who opposes that, is a traitor to the country. You put the people against each other.”

And that’s what’s happened. We’ve seen it in families. We’ve seen it in churches. We’ve seen it in businesses. We’ve seen it in cities. We’ve seen it in states. We’ve seen it in countries. I have colleagues in Italy that tell me right now, that the response that the non-vaccinated are receiving from the vaccinated people in Italy was the same response that they saw when Mussolini was in charge of Italy during World War 2. The same pressures, threatens, accusations; not a thoughtful discussion. You know?

If somebody is nuts, – you know, if this book is wrong, well I’ve pretty much laid out all the data; it’s – it would be easy to refute it. The problem is, I’ve laid out all the data. And you can’t refute it. The documents have been saved by the way, in case they try to pull them off the internet. They’ve been, they’ve been given to several sources for safe-keeping for hard copies, for use in courts around the world as we hold these people accountable.”

Mike Adams @26:24: “So once again, you’ve – we’re going to have to do more interviews, because you’re, you’re just flagging all of these things. Let me just, let me bring up the Stanford Prison Experiment. I’m sure you’re familiar with it, it was based on the Milgram Experiment, but the Stanford Prison Experiment, for the viewers who may not be familiar, they took volunteers, who I believe were Stanford graduate students, and they divided them up. Just, half of you are going to play the role of guards, prison guards, and the other half are going to play the role of prisoners. And then they role-played that for not very long, when the guards became, you know, diabolical, cruel, in their treatment. Because they began to adopt these psychological roles.

And that’s what you’re describing, Dr. Fleming. Where the vaccinated, now, become the prison guards of society. And where this is going is now very clear, because the CDC has a document on their website that we’re covering. It talks about “green zones”, which are COVID quarantine camps.

Governor Lee of Tennessee, just on Friday, signed an Executive Order authorizing National Guard and State Guard to take people away from their homes with telephone assessments, determining who needs to be taken away, to be put into involuntary internment camps, that are being constructed in the state of Tennessee. And the CDC saying we’re going to have “community level neighborhood enforcers” of some kind, who are checking in with you to make sure you’re complying.

This – this is, this is an Orwellian nightmare, come to life.”

Dr. Richard Fleming @28:00: “Yeah. This is Nazi, Germany. And by the way, Executive Orders don’t have legal authority if the legislative bodies is Mr. Executive, in this case, the governor, you don’t have the authority to do that.

And this is where I point it out earlier in our discussion. Anybody who takes the oath of office to uphold and defend the Constitution of the United States, and, same thing for their states, the supreme law of land in the United States is the U.S. Constitution. Statutes passed by the Congress of the United States and treaty law, it’s in the Constitution, violation of any of those by anybody who has an oath is a violation of the Constitution, is treason by definition. Treason is punishable by death. [Mike Adams: “By definition. Also. Yes.”]

By definition. Violation of the Biologic Weapons Convention treaty, the ICCPR treaty, the Nuremberg Code, and the Helsinki Declaration, are international treaty violations before the International Criminal Court, is – are crimes against humanity, just as they were in Nuremberg. So I’m calling for Nuremberg 2. We are much closer to that than anybody else has and perhaps I’ll come back another day to let you know exactly where we’re at on that. [Mike Adams: “We need that update, yes.”] 

These crimes are crimes against humanity, and they are punishable by death, just like they were in Nuremberg, and bear – remember, that in Nuremberg, there wasn’t just one trial. There were a dozen of them. After the first trial, came the doctors trial, and the couple after that the jurists, or the judges, and the attorneys and the law-maker trials. They were all held accountable in International Court for crimes against humanity.”

Mike Adams @29:57: “How – I don’t know, the historical record in detail. How many people were sentenced to death for being complicit in that?”

Dr. Richard Fleming: “Um, I’ve actually got that on the site in some of the presentations I’ve done so I know. I can try to really pull up, real quick, one of the PowerPoint slides.”

Mike Adams: “While you’re looking for that, let me just tell the audience that the title of your book is, “Is COVID-19 a Bioweapon?” It’s currently available on Amazon, somehow. I’m not sure how. They’ll probably pull it at some point. So get it while you can. “Is COVID-19 a Bioweapon?”

Dr. Richard Fleming: “So, there were, in the initial trial, of the 24 defendants, with Goering and the rest, of the initial 24, 12 were given the death sentence. 3 were given life imprisonments. 4 were sentenced between 10 and 20 years. None of them received the treatment that they wanted. Some of them thought, well, we were – they were German high officials, they should be treated with more respect. And the court just laughed at that.

And then there were a couple, Hitler and Goering – or Goebbels, both committed suicide before the war came to an end. And Goering laughed at them and committed suicide the day before they were going to execute him. There were 12 trials, after that one came the doctors trial, and 7, there were 7 German doctors who argued that they weren’t doing anything different than American and other – and Russian doctors were doing. And the truth of the matter is, they really weren’t doing things worse. But they were physicians – excuse me, they were physicians who came up and said, the problem with that is that these things were wrong no matter who did it and we’re not going to let them get by with it. So that was the Nuremberg Code that was developed. And uh… let’s see… if I have that numbers on that.

Of the 16, let’s see, of the 23 doctors, 16 were found guilty, and 7 were executed. [Mike Adams: “Wow. Wow.”] So if you think you get by free on this one, um, you don’t. Because as long as I’m still living and breathing, I plan to see this through. Because this is a violation. This is a violation of science. This is a violation of medicine. This is a violation of humanity.”

Mike Adams @32:40: “What will it take, Dr. Fleming, before we can have that kind of public pressure to call for Nuremberg 2.0? Because, you know, looking back at World War 2, they – the Nazi regime got away with genocide for many years. Murdered millions of people, while these so-called good Germans went along with it. And it was happening in their own backyards; they wanted to be part of the party. One of the economic benefits of having the war factories running, and so on. We have a lot of good Germans in America today, I’ve noticed. Because they’re going along with it. It might be half the country at this point. Going along with it.”

Dr. Richard Fleming @33:19: “Yeah, there’s a nice sign that I’ve seen that I’m sure has been spread around through our social media system that we have. Where it says, “If you wondered what you would’ve done in Nazi, Germany 1930’s, you now know.” 

Mike Adams: “That’s right. That’s right. And, you can look at your friends, family members, co-workers, whatever, you can now tell who would’ve been right at home in the Nazi regime.

Dr. Richard Fleming @33:43: “Here’s the important thing your listeners need to realize. The people that recognize there’s a problem, need to reach out to the people who have been taken advantage of. Because most of the people who get vaccinated, for example, did so because they were worried about someone they loved and care about.

Vaccines don’t keep you from getting infected. For them to work, you have to get infected. Okay? Vaccines don’t keep you from spreading infection. They simply make it possible for your body to respond sooner, to whatever you get vaccinated with so that your symptoms are shorter in duration. Which is a great way to increase asymptomatic carriers. Or minimally symptomatic carriers. And the problem is, it doesn’t do a thing for the pressure strains of the variants that exists. And those are going to continue.

These viruses have a lot of variants, we’re tracking, I as a research scientist, I’m actually watching the data that’s being done on the changes in these viruses to watch what’s going on. To watch what changes are occurring, what changes are happening naturally, evolutionary wise to this virus. Because even though it was man-made, it’s still a virus. It’s a living thing, and it’s making the changes like living organisms do.

Some of it looks like it’s trying to delete some of the inserts that were put into it. The consequences of some of that is becoming even more infective, but it’s not becoming more dangerous. Remember that if a virus becomes too dangerous, it will kill whatever it’s in, and then it can’t spread. So it’s not like these things become more dangerous. They get dangerous enough to get their benefit, naturally, and when idiot humans work on them and make them – well, all bets are off.

And what we saw was an ideal bioweapon, because the idea of a bioweapon isn’t to kill your enemy. We learned in Vietnam, my era, that if you wanted to win, you didn’t shoot to kill your enemy; you shot to maim your enemy because a wounded soldier on the other side might have friends that will come to the rescue of their friend and drag them off the field. Right? Now instead of killing one person, you’ve taken 2 or 3 people off the field. So maiming is much more effective.

Now if you can demoralize and damage a society by putting it – I don’t know – by shutdown and economic tailspin and, and keeping its people from talking, you have developed the ideal bioweapon.”

Mike Adams @36:18: “But, to that point, the people who built this, and the people who have pushed this and promoted the hysteria, they have gained so much power and profit. Also through the assertion of false authority, like the CDC claiming they now control all private property rental contracts, somehow, for some reason out of the blue. But why wouldn’t they now release something more dangerous and more deadly if they have it in the freezer? You know, the Fauci Freezer 2.0. Why wouldn’t that now be their next play?”

Dr. Richard Fleming @36:52: “There isn’t any reason why it wouldn’t be. Remember earlier I made the comment that research scientists don’t stop and say, “Okay, I guess we’re done with this project. Let’s go home.” They’re constantly working on it. You know, if you got the people doing what you want the people to do, well, you now have a perfect setup for continuing to run your experiment. You know? And which may not be the way people want to think about it, but it’s, from that point of view, it’s a great experimental design of ‘what can we get by with what can we do?’

And one thing that, you know, I didn’t mention before, I was working in my Master’s in psychology before I entered medical college. And so we had done all the work on these types of things, as graduate students in psychology, including the Stanford study and things like that. And it’s amazing what people will do. They will do it because they like power and control. They will do it because they don’t want to be hurt, and so they’d rather go along with it. It’s very easy to turn people against people.

But again, going back to the idea, if you can reach out to your neighbors and your friends and the people that maybe you’ve been alienated from, and say, “You know, this isn’t us. This isn’t us fighting us.” We’ve gotta stop fighting us and start looking at the science and the information. Which is what this book does, “Is COVID-19 a Bioweapon?” tells you what you need to know.

Well you can go find it, and prove for yourself because – like Galileo? You know? He got put under house arrest for telling everybody – most people think he got put under house arrest for saying the Earth goes around the sun. What he got put under house arrest for was saying, “You know what? Don’t take my word for it. And don’t take anybody else’s word for it. If you look up at the sun and the stars and the moon, and you think about these few things… you know what? You’re smart enough to figure this out on your own.”

And oh my goodness. Do we really want people having common sense and saying, wait a minute. If this approach was so good, why would we have to offer Krispy Kreme donuts, and marijuana, and lottery tickets, and major league baseball tickets – I mean, we wouldn’t have to bribe the American people for doing that.

Recognize that, as a research scientist with 53 years, if these drug vaccines had actually been tested properly, and done correctly so that they produce the desired end result? I’d be the first person in line saying, “Go get ’em!” That’s not what you’re hearing. What you’re hearing, is that’s not what’s going on, and these are the people who built it.”

Mike Adams @39:26: “Okay, your experience in psychology leads me to this next question. One of the things that we find, in trying to reach out to people, is that those who have already taken the vaccine, then, they of course are now looking for data and filtering out anything, so that they can reinforce their previous behavior. So they’re taking the vaccine, they cannot cognitively accept contradictory information that would show, retroactively, that they made a bad decision. That phenomenon is very real.”

Dr. Richard Fleming @39:57: “Right. Right. But here’s the good news for them. Because part of the problem for them is that they’re going, “Well, if I accept that, now it means… I’m in trouble. And the people that I thought I was protecting are in trouble.”

Well here’s the good news. Number one: it turns out that we did research on people that had the infection or developed COVID-19 and we showed success in 99.83% of the cases by treating the inflammation, the blood clotting and the attachment of the virus and its ability to replicate. So with the stress of all this, I actually put together a protocol based upon prior published research, from lots of different people. You can go to the website, the one area of published research on SARS has more than a hundred and sixty research papers on it.”

Mike Adams @40:47: “And this is all at flemingmethod.com?”

Dr. Richard Fleming: “Flemingmethod.com. That will explain these different drugs, and the vaccines themselves. The EUA documents. And drugs that work and why they work.

So one of the examples is, Ivermectin has not been known, the way I do it, with tissue measurement, to interfere with the attachment of replication of the virus. What it has been shown to do, is protect the nucleus of the cell from being, from having genetic material from outside the cell get into your cell and become part of your DNA.

So one of the problems of the vaccines, is it’s dumping BILLIONS, versus hundreds of viral particles, but BILLIONS of genetic codes for spike proteins. And we’re talking for Pfizer/Moderna, 13.1 billion, and for Janssen and AstraZeneca, 50 billion. You know. In Novavax it’s nothing more than just dumping in a load of that spike protein made inside moth cells. And God knows what’s actually in the spike protein since it had to get in the DNA of the moth cell to then be made.

I mean, you know, at what – I don’t know. Right? Because they’re not actually showing it, so injecting that is not more intelligent. It’s injecting spike proteins made by moth cells, into you, with probably something else.

And so, what these protocols that I put on the website for people who have been vaccinated or have shedding problems, which we know shedding’s a real thing because the FDA and Health and Human Services published 2 papers: 1 in August of 2015, talking about, what do you do with mRNA and DNA viral and bacterial gene therapies? Their words, not mine. And then in January of 2020, came out with an updated report, FDA and Health and Human Services and CDERs on the shedding byproducts are the products of what you inject in the body. Which are, you know, spike protein and who knows what else? Right?

So as a result of that, we’ve put together the best evidence available, treatment protocols, and we have been testing that in Europe and some places in the United States, and we’re seeing positive results from people. So we know the sooner that gets started the better, and, you know, if you’re not symptomatic, you don’t see anything, you know, you have nothing to measure. But it’s not a done deal just because you got vaccinated and you had problems or you’re concerned about it.

We know from the animal models right now that the humanized mice developed brains that look like sponges; so what I would call spongiform encephalopathy, and what the general public calls mad cow disease. We know the rhesus macaque animal models – the rhesus macaque animal models showed Lewy bodies, which causes Alzheimer’s disease in the brains of all the animals that were given these spike proteins. We know this is true whether you get it naturally or by the vaccine. The difference is that these drug vaccine biologics have BILLIONS compared to hundreds or thousands. Right? So you don’t have to be a rocket scientist. You don’t have to have a PhD, MD, JD to figure this out. You know, my parents would have told you, “Yeah, billions versus hundreds, big difference.”

Mike Adams @44:12: “But, but I’ve actually, I’ve heard from people who were trying to justify why they took the vaccine, and they would actually tell me that they wanted the smallest possible exposure and that the vaccine could provide that. And I said, “Are you kidding me?” I mean, that’s not a small exposure. What are they injecting – 250 microliters? And, you know, spike protein particles are really tiny. So there’s a lot of ’em in there.”

Dr. Richard Fleming @44:37: “Yeah, when you do the math, and you can – there’s actually, I’ve got that on the website so you can do the math based upon the volume, and for the lipid nanoparticles, Pfizer and Moderna, it’s 13.1 BILLION. And Janssen and AstraZeneca it’s 50 BILLION. Okay? [Mike Adams: “Incredible.”]

And you have to understand, once you appreciate that this spike protein is a man-made gain of function bioweapon, and then you realize that the vaccines are nothing more than the genetic code for the bioweapon, now you realize that the vaccines ARE the bioweapon. In addition to the virus.”

Mike Adams @45:16: “But, what you’re saying makes perfect, logical, rational sense. But how can mainstream doctors be so self-convinced it seems, when you can give them research. Hey, the Salk Institute says the spike protein causes widespread vascular damage, and the spike protein is IN the AstraZeneca vaccine that’s been linked to blood clots and so on. And they will – they will somehow, they will delete that from their consciousness. They will say that they don’t believe there is a spike protein. Or that they think that that antigen target is harmless. They just delete, from their consciousness – It’s like, it’s like mass hypnosis or something. Really.”

Dr. Richard Fleming @45:27: “Yeah, and one of the reasons we’re having so many papers – that 160+ papers and it’s growing every day, on the website, is doctors do want to do the right thing, by and large. But they haven’t had the data. They haven’t known where to go look for it. And they haven’t had the data to look and say, “Wait a minute. This was a gain of function bioweapon. This was something man-made.”

The benefit of putting this information out there, for the general public to read, and for the doctors to read, is to bring everybody up to speed. You know, last year, a year ago, I’d have said, “You know what, doctors? I get it. You’re just going along with what we’ve done before. We know vaccines can be beneficial for people.”

I’m not anti-vaccine. I’m just anti-bad medicine. Okay? People have heard me say that now probably too much. But I’m just anti, anti-stupidity, okay? Richard doesn’t suffer fools gladly. That’s what my original mentor used to tell people. And I don’t. I don’t. I don’t care what position or power, authority they have. And the more of that they have, the more responsibility they have to be honest and upright, and honest with people.

So the truth of the matter is, a year ago, I could give a break to my medical colleagues and say, “Okay, you just didn’t know. You were going along with what’s been taught. But look guys. We’ve never seen this much of a blithering disaster before in our lives.” Right?

I mean, we’ve never had a problem where we’ve promoted a variant that’s more infective of something as a result of the vaccines we’ve done. Our vaccines in the past have taken a virus, say… measles. Okay? And we’ve taken the whole, the whole family of measles, right? You know, because there’s not one thing. It’s just one human, right? Humans vary, but they’re all humans. There’s not one type of bacteria, you know, e. coli, but there’s a variety of them, but they’re all e. coli. Well there’s not just one type of SARS-CoV-2. There’s varieties of those.

So in the past we’ve always taken those viruses, we’ve weakened them, attenuated them, and then injected it into people. So what did people see? They saw all of them. And they saw all the parts of the virus. So they didn’t just see a spike protein. They saw the nucleocaps, and the envelope, and the HE and all the other components of it that they can then make antibodies to, and t-cell responses to. So if they saw any of that in the future, they responded.

What did we do this time around? We didn’t give you the whole thing. We gave you the genetic code of a bioweapon, of one type of spike protein, so that the further you get away from that, the less likely you’ll respond to it, and you won’t recognize the virus if you get a variant of it for real, because not only will the spike protein be different, but you’ll never have had any exposure, the HE component, or the envelope component, or the nucleocapsid component. So it’s all brand new to you; you’ve got NO immunity.

And there’s papers that have been published that show that people with natural exposure to SARS-CoV-2 have long lasting natural immunity with t-cell and antibody major responses – it doesn’t matter how bad the exposure was or how bad the infection was. And there’s data that shows that there’s no relapse for people who have had influenza A inside a megalovirus. 

Mike Adams @49:14: “Yeah, robust natural immunity was the term. Now, now Dr. Walensky of the CDC has admitted a recent quote. She said that we’re only a couple of mutations away from the original vaccines being completely ineffective. So, she’s saying what you just said. I mean, she’s confirming it. That’s almost a direct quote from her. It’s astonishing! Even they realize their vaccines are failing.”

Dr. Richard Fleming @49:40: “This is a dog chasing its tail. And while that’s fun to do with a dog, particularly if it’s your dog and you like him, okay? This isn’t exactly the same thing, is it? I mean, people – people are dying, because they get infected and then when they get ill, they’re not getting treatment. That doctors KNOW work. Okay? These agencies do not have the legal authority to be telling doctors not to use these treatments. [Mike Adams: “It’s extraordinary.”]

Agencies don’t have the right to ship people off to camps. That governor, doesn’t have a legal right in his state, to do that. His legislature needs to step up, the people in that state need to look at their elected officials and go, “Guys. You want to be elected next term? You need to put a hold on this. You don’t have this authority.” This did not become the Third Reich/Fourth Reich in the last 2 years. Even though they’ve been playing with this for 3 decades.”

Mike Adams @50:41: “Well, knowing some people from Tennessee, I have a feeling there’s going to be a shorter John Rope coming up real soon. But we’ll, we’ll leave that to people’s imagination.

Let me ask you about inflammation. This is our last 5 minutes here. You’re an expert on inflammation and I think one of your patents you said relates to the measurement of inflammation in tissues. I want to ask you about your estimate of the progression of the inflammatory response, specially based on the mRNA technology that’s causing people to generate these spike protein bioweapons in their bodies.

And again, the Salk Institute says, yeah, these spike protein cause vascular damage. We’ve seen blood clots, especially in young, healthy males with otherwise healthy cardiovascular function. We’ve seen myocarditis, we’ve seen strokes, we’ve seen heart attacks, lots of things.

What’s the prognosis if people don’t do the things that you describe on your website? Because there are interventions that can be post-vaccine interventions, that can help tremendously. But if they don’t do those things, because it’s all being censored, what’s the progression that we can expect to see even antibody dependent enhancement?”

Dr. Richard Fleming @51:46: “Yeah, so an antibody dependent enhancement is very unique to this virus. Which is also another trigger for you to realize that it’s not a naturally occurring one. Because in this virus, the antibody dependent enhancement is actually the result of antibodies being made to the end terminal domain of the spike protein. And when those antibodies attach, they open up the spike protein and make it 4 to 10 times as infective. That’s the real antibody dependent enhancement.

It’s different than anything we’ve seen before. But this is – so the body is going to produce this InflammoThrombotic Response that I talked about originally in ’94 or ’95, put in my textbook in ’99. Did the bacterial work from 2000 to 2003 and was on 20/20 talking about it in 2004, so you would’ve thought we’d have this down by now. But your body sees something infected, whether it’s a spike protein or the virus, and it dumps chemicals from your t-cells to try and kill anything that’s been attached to it, to try to stop the replication of the virus. That happens at about 3-5 days, and then in 7-10 days your b-cells kick in and do much of the same thing chemically, but then also make antibodies. Right? So they’re going to go in and they’re going to attach to that tissue.

Now, all you need to go back and do is look at strep pharyngitis, when people get strep throat and doctors like myself say, particularly cardiologists like myself say, ‘you need antibiotics for that’. Why do we write that? Because those antibodies that respond to streptococcus pneumoniae, or what you call strep throat, also recognize the valves of your heart as looking an awful lot like it, and produce rheumatic heart disease. There’s different heart valves. And over the course of time, you’ll end up with a valve replacement. So when these attacks occur on your heart, if you don’t stop them sooner than later, it causes inflammation and damage and weakness to the heart. And the longer that goes on, the more that damage is going to occur and it’s going to add up over the course of time.

And you’re going to take, for the love of God, vaccinating our kids, and – and you know, all the way down, and our college students, our university students, our athletes, with these – these vaccines that are producing, we know, 6,000 cases so far reported on VAERS of heart attacks, or damage/death to the heart. And cardiomyopathies, or inflammation of the heart that produce viral cardiomyopathies – that we’ve known about since, I don’t know, at least I – when I was in medical school in the Dark Ages in the early 80’s, 1980’s, it’s going to get progressively worse and worse and worse.

We know from the animal models that the brain disease that occurs in those animals means that at about a year and a half, we’re going to start seeing this occur in people. Now it’s going to depend on how much they got exposed to, and how much got into the brain, how much damage was done to the heart. But we’re going to see these progressive diseases take more and more of a toll if people don’t take action to address them.”

Mike Adams @54:46: “Well Dr. Hoffe from Canada has spoken about using d-dimer tests, I believe to – and some microscopy, to look at micro blood clots in the vascular system of post-vaccine patients. And he’s expressed tremendous concern about medium term 2-3 years out, vascular damage that is accumulating and leading to severe cardio events. Have you seen what he’s talking about?”

Dr. Richard Fleming @55:16: “Yeah, FlemingMethod is the only way that – is the way that we monitored those treatments so we can fine-tune in our study what was going on. And you can monitor people every 3 days and you can see the change; you can see whether they’re getting better on the treatment or not making any change or getting worse. So this stuff doesn’t take a ton of time to start seeing any effect.

You know, once the immune system kicks in, 3-5 days for t-cells, 7-10 days for antibody production, from the delayed humoral response, and you’re going to start seeing damage occur. If you don’t do something about that damage, and you develop COVID-19 as a result, you’re going to see the consequences of that. A slow smoldering process is still a fire that’s burning. It may not end you up in the hospital, but it’s going to – and it’s going to depend on the person. How bad that turns out over the course of time. And we’re going to get to see it.”

Mike Adams @56:12: “I’ve got to ask you this question. I hope you can stay another couple of minutes, but, what about the proinflammatory properties of certain low-grade seed oils that are heavily used in the diet – such as soy oil, corn oil, and so on – perhaps canola. Do you think there’s kind of a confluence of synergistic toxic effects from COVID-19 vaccines, spike protein injections, and dietary factors such as proinflammatory ingredients?”

Dr. Richard Fleming @56:41: “Right, so the original theory that I talked about in 1994 that’s on the website, includes all of those factors together. I mean, basically I joined American Heart in 1976 as the youngest faculty member ever. And that put me on 3 major committees right upfront: Basic Cardiac Life Support, Advanced Cardiac Life Support, and the newly formed Physician Cholesterol Education Faculty.

So I went around talking about cholesterol and training physicians and the general public on all these different aspects. And then in 1994, after doing a lot of research on heart disease and diets and, you know, I was, I did several dietary studies; I’ve done more dietary studies that I ever wanted to do in my life, on the effect of various diseases including heart disease.

And in 1994 I walked into American Heart and I said, “Look guys, okay, I’ve been – I’ve looked at my data, I’ve looked at all the other data.” You know. I’ve looked at data outside of the U.S., outside of medicine; I’ve looked at everybody’s data. I had something like 5 or 6 hundred papers at that time, and I said, “Here’s the 12 things that I think play a role to varying degrees in different people. Much like a spider’s web, where you can tug on one part, it’ll affect everything else. And it produces this inflammation wall of the arteries, make it impossible for the arteries to relax and carry more blood flow, and that’s really what heart disease is.” And I got told I didn’t know what I was talking about, you know.

In fact, the HERS 2 trial, or HERS trial was coming out where they were talking about estrogen replacement, and I said, “Look. This is going to be a problem.” And they said, “No no no. We know this is going to come out well.” And that study they presented in ’94, they said, “Whoops. Look. So bad. This actually causes more heart disease.” And I said, “Really? You think so?”

Because what I was trying to tell people is, what are the general practice doctors, the family practice doctors usually do when they talk to young women that are just getting married and they say, “Doctor, I don’t want to have children right away. I want to just have time with my husband.” So they prescribe them birth control pill. Right? Estrogens, right? Right? And what’s the question the doctor says? “Well, you have any clotting problems in your family?” Why? Because we know that with the estrogens at that level, and clotting problems, you end up with problems.

Well, gee. I was part of the theory. So the theory said, yeah, cholesterol, triglycerides, saturated fats, highly processed foods, homocysteine, lipoprotein little a, fibrinogen, manipulation of things, bacteria, and viruses. All played a role, and some other things that I’d have to go look at the theory again. I put it in a nice schematic for people. All play a role to varying degrees.

So, when this hit, all SARS-CoV-2 did was, deformally prove the entire theory. Which wasn’t exactly what I was going for. But you know, back in the 90’s, I was working on these neuro five ac receptors, that I had concerns about as far as causing inflammation from animal, animal meats, and what was going – it turns out that that’s exactly what these people were working on the virus at the time, because the GP120 uses that same receptor. It’s called a sialic raft receptor, just to first hook into to help stabilize the virus to infect. But it’s also a prion region of that.

So, and when Shi Zhengli, as you’ll see in the book, put glycoprotein 120 in 2004, my original thought was she was doing it to try and get it into the nucleus of the cell, because she didn’t have that data. The Human Genome Project was being completed at that time showing that you didn’t need to do it that way. The cells would do it if you give them the right virus or bacteria. But what it did do is it anchored into the cell, and it’s a prion. And she knew that, because the data was already published in 2004 that showed GP120 produces prion diseases.

Well, it got put into the spike protein, along with everything else, produced another prion region of the spike protein that attached. That’s the regional binding site that attaches to the ace2 receptor. So, they knew this, they played with it, they intentionally did it, they knowingly did it. They violated international treaties. Violating informed consent violates more of those international treaties. So, yeah. All these things play a role.”

Mike Adams @1:01:01: “What if the, the Fauci 2.0 Special, that they might release next, this gets back to something you mentioned right at the very beginning, that the research was continuing into pushing what sounds like HIV portions, into the genetic code to achieve some sort of immunodeficiency effect? What if that’s the next bioweapon? It’s an aggressive, now novel bioweapon; none of the current vaccines touch it at all. It causes more vascular damage and it turns off the immune system. Wouldn’t that be kind of a global killer right there? Like a – like an extinction level, you know, attempt?”

Dr. Richard Fleming @1:01:41: “One of the things you’re going to see in the book is that there’s 1,770 nucleotide bases in the spike protein, that are identical to HIV and SIV, which is simian immunodeficiency virus. 

Mike Adams: “Okay. All right. So we’re not too far off the mark. Yeah, exactly. Wow. Well I hope, I hope – I mean, I can ask you questions for hours if you had the time, but I hope you’ll come back and do this again. You’re a fascinating individual, I really honor your courage in speaking out, but also the brilliance of your understanding of this. I think it – if science is to be saved at all, it’s going to be due to people like yourself, by the way. So thank you for what you’re doing. And thank you for joining us today.”

Dr. Richard Fleming: “Thank you. My pleasure to be here.”

Mike Adams: “Absolutely. Now, folks, Dr. Fleming’s book is, “Is COVID-19 a Bioweapon?” Check out his website, I’m going to: flemingmethod.com. Now I’m fascinated about all his research into inflammation prevention.

I’m drinking my turmeric smoothie right here. This is part of my anti-inflammatory response. My neuro-protective potion, right there.

So, spread the word, folks. This is going to be censored on youtube, but you are free to post it everywhere else. Thank you for watching. I’m Mike Adams, the founder of brighteon.com. Take care.”

Thank you to everyone reading and/or watching the interview. Please help spread the word and stay informed. Research is incredibly important, especially in these uncertain times and with the incredible amount of propaganda and deliberate media suppression.

Thank you to everyone exposing these corruptions.