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Vaccine critic in the EU Parliament: “Covid-19 was an act of biological warfare against humanity”

The criticized covid vaccinations

Published 31 May 2023
– By Editorial Staff
Dr David Martin spekas at the EU-parliament at the International Covid Summit III.
13 minute read

The high-profiled vaccine sceptic Dr David Martin, who describes himself as a financial analyst, author, commentator, professor and researcher, declared during the International Covid Summit in the European Parliament that covid-19 was in fact “a form of biological warfare” deliberately unleashed by the US government to create a global pandemic, benefit the pharmaceutical giants and promote mass vaccination programs.

In early May, the third edition of the International Covid Summit was held in Brussels, sponsored by the EU groups European Conservatives and Reformists and Identity and Democracy.

A large number of guests and speakers were invited, including American biochemist Dr. Robert Malone, who is also the inventor of the mRNA vaccine technology.

During the conference, experts, activists and EU parliamentarians discussed the possibility that covid-19 was deliberately used as a “weapon” to impose draconian control over citizens, shut down societies and benefit certain actors financially, as well as the seemingly deliberate manipulation of corona statistics by Western health authorities and the health risks associated with the controversial vaccines.

One of the participants was Dr. David Martin, a high-profile vaccine critic and debater, and what he had to say about the virus has shocked millions of people around the world. Martin argues that a coronavirus was first identified in 1965 and that powerful interests have worked for over 50 years to manipulate and modify the virus, turning it into a “biological weapon” that was deliberately released to harm humanity and benefit the pharmaceutical giants and other special interests.

Below the full transcript of Dr. David Martin’s controversial speech in the EU Parliament:

 


 

It is a particularly interesting location for me to be sitting today, given that over a decade ago I sat in this very chair right here in the European Union Parliament.

And at that time I warned the world of what was coming, during that conversation that was hosted at the time by the Green and EFA and a number of the other parties of the European Unions, of various representations.

We were having a conversation on whether Europe should adopt the United States policy of allowing for the patents on biologically derived materials.

And at the time I urged this body and I urged people around the world that the weaponization of nature against humanity had dire consequences.

Tragically, I sit here today, with that unfortunate line that I don’t like to say, which is “I told you so.”

But the fact of the matter is, we’re here not for a reprisal on past decisions. We’re here to actually, once again, come to the face of the human condition and ask the question, who do we want to be?

What do we want humanity to look like?

And rather than seeing this as an exercise in futility, which is very easy from time to time when you’re in the position I’m in, I actually see this not as an exercise in futility.

I see this as one of the greatest opportunities that faces us because we now have a public conversation, which is now front and center in people’s minds.

When this was an esoteric conversation about biological patents, nobody cared.

But when that conversation came home, then it became something people can care about.
So I’m actually quite grateful for this opportunity.

I thank the members of Parliament for hosting this.

I thank all of the translators who I apologize in advance.

I will use terminology that is probably very difficult to translate, so my apologies, and I’d also like to acknowledge the fact that many of you are aware of my involvement with this in large part due to the amazing work of my wonderful wife, Kim Martin, who encouraged me at the very early days of this pandemic to get on front of the camera and talk about all the information that I had been sharing among very small groups around the world.

And it was in fact her encouragement that put me in a place where many of you have heard what I have to say.

Ironically, the world that I came from that used to be very popular, my CNBC and Bloomberg presentations, which were televised on mainstream media around the world, was an audience that I lost.

I can confidently say Covid diminished my fame, but I can also confidently say that I’d rather stand among the people with whom I’m standing today than any of the folks that were part of that previous world. So, this is a much better place to be.

My role today is to set the stage for this conversation in a historical context, because this did not come in the last three years.

This did not come in the last five or six years.

This actually is an ongoing question that probably began here in Europe in the early stages of the mid 19 hundreds, but certainly by 1913, 1914, this conversation started right here in Central Europe.

The pandemic that we alleged to have happen in the last few years also did not happen overnight.

In fact, the very specific pandemic using coronavirus began in a very different time.

Most of you don’t know that Coronavirus as a model of a pathogen was isolated in 1965.

Coronavirus was identified in 1965 as one of the first infectious, replicatable viral models that could be used to modify a series of other experiences of human condition.

It was isolated once upon a time associated with the common cold.

But what’s particularly interesting about its isolation in 1965 was that it was immediately identified as a pathogen that could be used and modified for a whole host of reasons.

And you heard me correctly, that was 1965.

And by the way, these slides are public domain.

You’re welcome to look at every single reference.

Every comment that I made is based on published material.

So do make sure that you look at those references.

But in 1966, the very first COV Coronavirus model was used as a transatlantic biological experiment in human manipulation, and you heard the date 1966.

I hope you’re getting the point of what I’m saying.

This is not an overnight thing.

This is actually something that’s been long in the making.

A year before I was born, we had the first Trans-Atlantic coronavirus data sharing experiment between the United States and the United Kingdom.

And in 1967, the year I was born, we did the first human trials on inoculating people with modified coronavirus.

Isn’t that amazing?

56 years ago, the overnight success of a pathogen that’s been 56 years in engineering, and I want that to chill with all of you.

Where were we when we actually allowed in violation of biological and chemical weapons treaties?
Where were we as a human civilization when we thought it was an acceptable thing to do to take a pathogen for the United States and infect the world with it?

Where was that conversation and what should have been that conversation in 1967?

That conversation wasn’t had. Ironically, the common cold was turned into a chimera in the 1970s, and in 1975, 1976 and 1977, we started figuring out how to modify coronavirus by putting it into different animals.
Pigs and dogs.

And not surprisingly, by the time we got to 1990, we found out that coronavirus as a infectious agent was an industrial problem for two primary industries, the industries of dogs and pigs.

Dog breeders and pigs found that Coronavirus created gastrointestinal problems, and that became the basis for Pfizer’s first spike protein vaccine.

Patent filed. Are you ready for this In 1990?

Did you hear what I just said?

Operation Warpspeed.

I’m sorry.

Where’s the warp and the speed?

Pfizer 1990.

The very first spike protein vaccine for Coronavirus.

Isn’t that fascinating?

Isn’t it fascinating that we were, we were told that, well, the spike protein is a new thing.

We just found out that that’s the problem.

No.

As a matter of fact, we didn’t just find out it was not just now.

Now the problem, we found that out in 1990 and filed the first patents on vaccines in 1990 for the spike protein of Coronavirus.

And who would’ve thought Pfizer?

Clearly the innocent organization that does nothing but promote human health.

Clearly, Pfizer, the organization that has not bought the votes in this chamber, in every chamber of every government around the world, not that Pfizer, certainly they wouldn’t have had anything to do with this, but oh yes, they did.

And in 1990 they found out that there was a problem with vaccines.

They didn’t work.

You know why they didn’t work?

It turns out that Coronavirus is a very malleable model.

It transforms and it changes, and it mutates over time.

As a matter of fact, every publication on vaccines for Coronavirus from 1990 until 2018, every single publication concluded that Coronavirus escapes the vaccine impulse because it modifies and mutates too quickly for vaccines to be effective.

And since 1990 to 2018, that is the published science ladies and gentlemen, that’s following the science, following the science is their own indictment of their own programs that said, it doesn’t work.

And there are thousands of publications to that effect, not a few hundred. And not paid for by pharmaceutical companies.

These are publications that are independent scientific research that shows unequivocally including efforts of the chimera modifications made by Ralph Bairc in the University of North Carolina Chapel Hill.

All of them show vaccines do not work on coronavirus.

That’s the science, and that science has never been disputed.

But then we had an interesting development in 2002, and this date is most important because in 2002, the University of North Carolina Chapel Hill patented, and I quote, an infectious replication defective clone of coronavirus.

Listen to those words …

Infectious replication, defective.

What does that phrase actually mean?

For those of you not familiar with language, let me unpack it for you.
Infectious replication.

Defective means a weapon.

It means something meant to target an individual but not have collateral damage to other individuals.
That’s what infectious replication defective means.

And that patent was filed in 2002 on work funded by NIAD’s Anthony Fauci from 1999 to 2002, and that work patented at the University of North Carolina Chapel Hill mysteriously preceded SARS 1.0 by a year.
“Dave, are you suggesting that SARS 1.0 wasn’t from a wet market in Wuhan?”

“Are you suggesting it might have come from a laboratory in the University of North Carolina Chapel Hill?”
No, I’m not suggesting it.

I’m telling you that’s the facts we engineered SARS.

SARS is not a naturally occurring phenomenon.

The naturally occurring phenomenon is called the common cold.

It’s called influenza-like illness.

It’s called gastroenteritis.

That’s the naturally occurring coronavirus.

SARS is the research developed by humans weaponizing a life system model to actually attack human beings, and they patented it in 2002.

And in 2003, giant surprise, the CDC filed the patent on Coronavirus isolated from humans in violation once again of biological and chemical weapons, treaties and laws that we have in the United States, and I’m very, very precise on this.

United States likes to talk about its rights and everything else, and the rule of law and all the nonsense that we like to talk about, but we don’t ratify treaties about, I don’t know, defending humans.

We conspicuously avoid that we actually have a great track record of advocating for human rights and then denying them when it comes to actually being part of the international community, which is a slightly problematic thing.

But let’s get something very clear.

When the CDC, in April of 2003 filed the patent on SARS Coronavirus isolated from humans, what did they do?

They downloaded a sequence from China, and filed a patent on it in the United States.

Any of you familiar with biological and chemical weapons treaties knows that’s a violation.

That’s a crime.

That’s not an innocent, oops; that’s a crime.

And the United States Patent Office went as far as to reject that patent application on two occasions until the CDC decided to bribe the patent office to override the patent examiner to ultimately issue the patent in 2007 on SARS Coronavirus.

But let’s not let that get away from us, because it turns out that the RT PCR, which was the test that we allegedly were going to use to identify the risks associated with coronavirus, was actually identified as a bioterrorism threat by me in the European Union sponsored events in 2002 and 2003, 20 years ago that happened here in Brussels and across Europe.

In 2005, this particular pathogen was specifically labelled as a bioterrorism and bioweapon platform technology, described as such.

That’s not my terminology that I’m applying to it.

It was actually described as a bioweapons platform technology in 2005.

And from 2005 onwards, it was actually a bio warfare enabling agent.

It’s official classification from 2005 forward.

I don’t know if that sounds like public health to you, does it?

Biological warfare enabling technology that feels like not public health, that feels like not medicine, that feels like a weapon, designed to take out humanity.

That’s what it feels like, and it feels like that because that’s exactly what it is.

We have been lured into believing that EcoHealth Alliance and DARPA and all of these organizations are what we should be pointing to.

But we’ve been specifically requested to ignore the facts that over $10 billion have been funnelled through black operations, through the check of Anthony Fauci and a side-by-side ledger where NIAD has a balance sheet, and next to it is a biodefense balance sheet.

Equivalent dollar for dollar matching that no one in the media talks about, and it’s been going on since 2005. Our gain of function moratorium.

The moratorium that was supposed to freeze any efforts to do gain of function research.

Conveniently, in the fall of 2014, the University of North Carolina, Chapel Hill received a letter from NIAD saying that while the gain of function moratorium on coronavirus in vivo should be suspended, because their grants had already been funded, they received an exemption.

Did you hear what I just said?

A biological weapons lab facility at the University of North Carolina Chapel Hill received an exemption from the gain of function moratorium so that by 2016 we could publish the journal article that said SARS Coronavirus is poised for human emergence in 2016 and what, you might ask Dave, was the coronavirus poised for human emergence?

It was WIV ONE.

Wuhan Institute of Virology Virus One.

Poised for human emergence in 2016 at the proceedings of the National Academy of Sciences, such that by the time we get to 2017 and 2018, the following phrase entered into common parlance among the community, there is going to be an accidental or intentional release of a respiratory pathogen.

The operative word, obviously in that phrase, the word release, does that sound like leak?
Does that sound like a bat and a Pangolin went into a bar in the Wuhan market and hung out and had sex?

And, and lo and behold, we got SARS Cov-2. No accidental or intentional release of a respiratory pathogen was the terminology used.

And four times in April of 2019, seven months before the allegation of patient number one, four patent applications of Moderna were modified to include the term accidental or intentional release of a respiratory pathogen as the justification for making a vaccine for a thing that did not exist.

If you have not done so, please make sure that you make reference in every investigation to the premeditation nature of this, because it was in September of 2019 that the world was informed.

That we were going to have an accident or intentional release of a respiratory pathogen so that by September, 2020 there would be a worldwide acceptance of a universal vaccine template.

That’s their words right in front of you on the screen.

The intent was to get the world to accept a universal vaccine template, and the intent was to use coronavirus to get there.

Let’s, let’s read this because we have to read this into the record everywhere I go.

“Until an infectious disease crisis is very real present and at the emergency threshold that is often largely
ignored to sustain the funding base beyond the crisis.”

He said, “we need to increase the public understanding for the need for medical countermeasures, such as a pan influenza or pan coronavirus vaccine.”

“A key driver is the media and the economics will follow the hype. We need to use that hype to our advantage to get to the real issues. Investors will respond if they see profit at the end of the process.”

Sounds like public health.

Sounds like the best of humanity.

No.

Ladies and gentlemen, this was premeditated domestic terrorism stated at the proceedings of the National Academy of Sciences in 2015, published in front of them.

This is an act of biological and chemical warfare perpetrated on the human race, and it was admitted to in writing that this was a financial heist and a financial fraud.

“Investors will follow if they see profit at the end of the process.”

Let me conclude by making five very brief recommendations.

The last slide, nature was hijacked.

This whole story started in 1965 when we decided to hijack a natural model and decide to start manipulating it.

Science was hijacked when the only questions that could be asked were questions authorized under the patent protection of the CDC, the FDA, the NIH, and their equivalent organizations around the world.

We didn’t have independent science.

We had hijacked science, and unfortunately there was no moral oversight in violation of all of the codes that we stand for.

There was no independent, financially disinterested independent review board ever empanelled around coronavirus.

Not once, not once, not since 1965.

We do not have a single independent IRB ever empanelled, around Coronavirus.

So, morality was suspended for medical countermeasures, and ultimately humanity was lost because we decided to allow it to happen.

Our job today is to say, no more gain of function research, period.

No more weaponization of nature period.

And most importantly, no more corporate patronage of science for their own self-interest unless they assume 100% product liability for every injury and every death that they maintain.

Thank you very much.

 

Dr David E. Martin

 


 

The full part 1 of the International Covid Summit III can be seen below Dr. David Martin’s speech begins at 12.55.

 

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US halts mRNA investment: “More risks than benefits”

The criticized covid vaccinations

Published yesterday 10:44
– By Editorial Staff
RFK points out that mRNA vaccines may be counterproductive - and prolong virus outbreaks instead of stopping them.
3 minute read

The US Department of Health and Human Services is halting the development of experimental mRNA vaccines. 22 contracts worth nearly $500 million are being terminated, citing that the technology poses significantly greater risks than benefits.

Health Secretary Robert F. Kennedy Jr. states that the decision was made following scientific reviews and consultations with experts at research institutions including the NIH and the FDA.

— One mutation, and the vaccine becomes ineffective. This dynamic drives a phenomenon called antigenic shift, meaning that the vaccine paradoxically encourages new mutations and can actually prolong pandemics as the virus constantly mutates to escape the protective effects of the vaccine Kennedy explains.

He particularly highlights the Omicron variant as an example of how mRNA vaccines failed to halt transmission despite widespread vaccination.

— A single mutation can make mRNA vaccines ineffective, the health secretary states, noting that “the same risk applies to flu”.

Wants to see “broader” strategy

According to Kennedy, the department’s conclusion is clear: the risks of mRNA technology outweigh the benefits when it comes to respiratory viruses.

— After reviewing the science, and consulting top experts at NIH and FDA, HHS has determined that mRNA technology poses more risks than benefits for these respiratory viruses.

Instead, the department will prioritize what Kennedy calls “safer, broader vaccine strategies”, such as traditional whole-virus vaccines and new platforms “that don’t collapse when viruses mutate”.

HHS clarifies that certain contracts already in final stages will be allowed to run their course, but no new mRNA projects will be initiated. BARDA (Biomedical Advanced Research and Development Authority), the federal agency responsible for advanced biomedical development, is now tasked with focusing on techniques “with stronger safety records and transparent clinical and manufacturing data practices”.

Critics were labeled conspiracy theorists

Many analysts warned early on that mRNA vaccines posed serious health risks, but were routinely dismissed as conspiracy theorists by both politicians and mainstream media.

Over time, however, a large number of serious vaccine injuries and deaths have been reported, particularly in connection with the extensive COVID-19 vaccination campaigns.

The criticism has not only concerned safety itself, but also the lack of long-term studies and authorities’ inadequate handling of adverse event reports. Against this backdrop, Kennedy’s announcement is seen by many as a long-awaited course correction.

Changed policy for children and pregnant women

The decision to halt mRNA contracts is not the only change. In recent weeks, Kennedy has also taken initiatives to remove the mercury compound thimerosal from influenza vaccines, in accordance with recommendations from the CDC’s Advisory Committee on Immunization Practices (ACIP).

He also welcomed the decision to no longer recommend COVID-19 vaccines for healthy children and pregnant women.

— There was a lack of any clinical data to support the repeat booster strategy in children, he stated.

Doctor testifies about vaccine injuries in US Senate hearing

The criticized covid vaccinations

Published 31 July 2025
– By Editorial Staff
The American anesthesiologist Dr. Robert Sullivan testified before the U.S. Senate in a hearing titled "Voices of the Vaccine Injured".
3 minute read

An anesthesiologist with 20 years of experience told US senators how he developed a life-threatening lung disease after covid-19 vaccination. Dr. Robert Sullivan was one of the witnesses in a Senate hearing on vaccine injuries held by the Senate Homeland Security Committee.

The Senate Homeland Security and Governmental Affairs Committee organized a hearing on July 15 titled “Voices of the Vaccine Injured” where people who claim to have been injured by covid-19 vaccines were able to share their experiences. Dr. Robert Sullivan, a licensed physician and certified anesthesiologist with over 20 years of active practice in Maryland, was one of the key witnesses.

Dr. Sullivan described a dramatic change in his health condition after vaccination. The same month he received his first mRNA dose, he had been featured in the Wall Street Journal’s fitness column for his aerial circus performances.

I was strong, healthy, and thriving. Just three weeks after my second dose, I couldn’t go up a flight of stairs without gasping for air, Sullivan told the senators.

The doctor developed constant chest pain, heart arrhythmias and overwhelming fatigue. An echocardiogram later confirmed damage to his heart and lungs.

The diagnosis was pulmonary hypertension. I had damage and narrowing of the blood vessels in my lungs, restricting blood flow and straining the heart. This isn’t like regular high blood pressure.  Pulmonary hypertension is usually progressive and fatal even with treatment. There is no cure, Sullivan explained.

The system didn’t respond

Dr. Sullivan reported his injury to VAERS (Vaccine Adverse Event Reporting System), the US system for reporting vaccine adverse events. Despite VAERS collecting his medical records, he never heard from the US health authorities FDA or CDC.

I believed in the system. I believed I would be heard. When I wasn’t, I channeled that disbelief into collaborating with the British Medical Journal on a report about the system’s failures. What I learned is chilling. If you are harmed, you are on your own., Sullivan said.

He explained that most doctors he knows have never heard of VAERS, and even fewer understand that there are mandatory reporting requirements. Sullivan was never taught about VAERS during his medical education and stated that it still isn’t taught.

Research predicted the problems

During his own research, Dr. Sullivan discovered that a scientist from Georgetown University had predicted exactly his type of injury in the same month the vaccines began rolling out.

He warned that spike protein, exposure, whether from the virus or from the shot, could harm the blood vessels in the lungs and placenta, Sullivan recounted.

The doctor referenced studies showing that spike protein from the SARS-1 virus also caused vascular damage in animals, and that many hospitalized covid patients develop pulmonary hypertension.

Broad vaccination perspective despite personal injury

When Senator Johnson asked about doctors’ attitudes toward vaccines, Dr. Sullivan surprised by explaining that he is still “enthusiastic about vaccination” and that he sees covid injections as something entirely different.

I’m not vaccine injured. I’m injured by an mRNA therapeutic. I was very careful in my testimony to use the word shot, Sullivan clarified.

He explained that training for vaccines is now limited to memorizing the schedule, but that the hidden cost of injuries is not studied or taught.

Spike protein toxicity

Senator Johnson raised the question of spike protein toxicity and criticized that many symptoms are now attributed to “long covid” instead of potential vaccine side effects.

There are many ways to lose with this new MRI technology. There are problems with the nanoparticle. There is a separate set of problems with synthetic mRNA. It persists in some people 700 days and counting now, Dr. Sullivan responded.

He explained that when the body is instructed to manufacture a protein that is presented on the cell surface, it creates a precondition for autoimmune disorders, and that the spike protein itself is biologically active.

—  It was published in December 2020, although not widely known, that that was causing damage to placenta and to lung, Sullivan added.

Dr. Sullivan concluded his testimony with an appeal for recognition and transparent information for patients, emphasizing the importance of truly informed consent in all medical treatment.

Study: Pfizer’s covid vaccine may cause eye damage

The criticized covid vaccinations

Published 22 July 2025
– By Editorial Staff
According to the study, the covid vaccine may cause the cornea to thicken and reduce the number of important cells that keep vision clear.
2 minute read

Turkish researchers have discovered that Pfizer’s covid-19 vaccine can cause changes in the eye’s cornea that could potentially lead to vision problems. The study, which followed 64 people over three months, shows that the vaccine can make the cornea thicker and reduce the number of important cells that keep vision clear.

The researchers measured changes in the cornea’s inner layer, the endothelium, before the first vaccine dose and two months after the second dose. The results showed that both doses led to thicker corneas, fewer endothelial cells, and greater variation in cell size.

Specifically, corneal thickness increased from 528 to 542 micrometers – an increase of approximately two percent. At the same time, the number of endothelial cells decreased from 2,597 to 2,378 cells per square millimeter, a loss of about eight percent.

“The endothelium should be closely monitored in those with low endothelial cell counts or who have undergone corneal transplantation,” the researchers warn in the study published in the journal Ophthalmic Epidemiology.

Short-term impact without symptoms

In the short term, the changes suggest that Pfizer’s vaccine may temporarily weaken the endothelium, even though patients did not experience any clear vision problems during the study period. For people with healthy eyes, these small changes are unlikely to affect vision immediately.

However, if the changes persist for several years, they could lead to corneal swelling or blurred vision, particularly in people with existing eye problems or those who have undergone corneal transplantation. A thicker cornea and reduced cell density can contribute to conditions such as corneal edema or corneal decompensation, which in severe cases can cause permanent vision loss.

Need for long-term studies

The research team emphasizes the importance of long-term studies to see if the changes persist months and years after vaccination. An ophthalmologist can use special microscopy to check if someone has a low endothelial cell count.

The study adds to a growing list of concerns regarding Pfizer’s covid vaccine. In May, the US Food and Drug Administration (FDA) forced Pfizer and Moderna to expand warning labels about risks of heart damage, particularly for men between 16 and 25 years old.

Pharmaceutical giant’s top researcher on covid vaccine: “Nothing was safe and effective”

The criticized covid vaccinations

  • Joshua Rys, a leading regulatory researcher at pharmaceutical giant Johnson & Johnson (J&J), now confirms on hidden camera what mainstream media dismissed as "conspiracy theories".
  • "Do you have any idea the lack of research that was done on those products?" Rys asks rhetorically in the clip, among other things.
  • The slogans "safe and effective" that surrounded the mass vaccination campaign were, in his view, a direct lie from the authorities.
  • "This was just, let's test it on some lab route models, analyze and see if it works and stuff like that, and just roll it to the wind and see what happens", he adds.
Published 16 July 2025
– By Editorial Staff
The hidden recording confirms many concerns that have surrounded the COVID vaccines.
1 minute read

Joshua Rys leads the creation and implementation of regulatory strategies for new and existing products within Johnson & Johnson in his role.

— We run the whole soup to nuts. Not only are we working on the products, but everything that has to do with the drug. We have to make sure that you understand how to use the drug, how to be able to prescribe certain pieces of information, how to communicate that to the patient, he explains his role.

In front of independent journalist James O’Keefe’s OMG hidden cameras, he confirms that Johnson & Johnson was well aware that the preparation was not safe and effective.

— Do you have any idea the lack of research that was done on those products? You shouldn’t be surprised that this happened. It was pretty much the government kind of made a deal with pharmaceutical companies and kind of pressured the pharmaceutical companies, because we’re not going to say no to the government.

— I mean, none of that stuff was safe and effective. We didn’t do the typical test. The typical process, that’s why it takes so long to get a product on market, the typical process is all this clinical trial testing and stuff in a small population, Rys continues.

— This was just, let’s test it on some lab route models, analyze and see if it works and stuff like that, and just roll it to the wind and see what happens, he adds.

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