“We do not believe any group of men adequate enough or wise enough to operate without scrutiny or without criticism. We know that the only way to avoid error is to detect it, that the only way to detect it is to be free to inquire. We know that in secrecy error undetected will flourish and subvert.” –J. Robert Oppenheimer
Gail Combs is being tormented by the volcanic devastation of blissful blogging that is WordPiss.
A little girl watches a mushroom-shaped cloud forming in the sky as the nearby Guagua Pichincha volcano near Quito, Ecuador, spouts boiling water and ash during the third consecutive phreatic eruption of the day 7th October 1999. (Photo by Martin Bernetti/AFP/Getty Images)
You must now suffer the heartache of placeholder.
This is a placeholder.
Most of this post is boilerplate, but with sprinkles of minor mirth.
Just as Wheatie’s Stormwatch Monday Open Thread was created as a place for people to openly express their thoughts and opinions, so, too, is this Wolfian Wednesday Persnickety Placeholder and Open Topic, where honest but civil discussion of all topics is encouraged. This thread is also to be known as Wolfie’s WOO-WOO Wednesday, due to the author’s expected rambling about his most WOO-WOO opinions. Please bear with us!
We are living in an episode of The Outer Limits.
Please label all AI-generated content as being such, unless it is patently obvious (e.g., humorous AI images). It is important that we as individuals not begin to pretend that socially derived artificial intelligence is actually our own, as this form of stealthy social information averaging and feedback would be one more pretense and deception between people, in service of stupid Marxist socialism, and of those who wish to substitute their communally protected lies for actual truth.
The source of alleged truth matters, not for the truth itself, but for validation.
And yes, it’s WEDNESDAY…again.
So are we halfway through the week? Is this really HUMP DAY?
Let’s try that again.
OK – maybe Wheatie’s rules need to be posted on Wednesday, too.
No food fights.
No running with scissors.
If you bring snacks, bring enough for everyone.
Other rules may be derivable from these, and that conjecture is left for discussion.
If there is nothing beyond the “W” below, then this is a pure placeholder. For health reasons, I can’t always post a timely opinion before each Thursday Wednesday, but I will try. Otherwise, you have this placeholder post, where YOU provide the content. Enjoy!
How did Q put it? Ah, yes.
“Enjoy the show!”
W
OK, people. I was going to use this placeholder to post about a recent essay by Robert Malone, regarding MAHA and Robert F. Kennedy, Jr. This is a great essay, and I hope you will read it.
Let me just pull a teaser out of this essay. It is a preface of a book by a naturalist and explorer, who was a member of the wealthy family that brought you Tabasco Sauce.
Yup. Tabasco Sauce. That man was a friend of Malone’s great-grandfather.
Here is the quote:
Let those who would live happily and approach the inevitable with a peaceful mind, take heed to nature’s teachings, live a natural life; watch, listen, and think; for the more of these three things you do, the sooner you will realize that your happy, natural fate, lies solely in yourself and your life on earth, and not in the future.’
-McIlhenny
It’s a nice essay that I think many of us “older” people will enjoy.
How to Distinguish a Key Principle of Reason, Logic and Science, from Irrational Exuberance in Contrarian Explanation
I really try to avoid using the term crackpot.
In science, the term crackpot is a bit like the terms Nazi, pedophile, and antisemite are in politics. The word freezes conversation. It strikes fear – often very unfairly – into all who are listening. Indeed, it is used in science for that very reason. Crackpot is very similar to the word crank, only worse. Using it in regards to a single person rarely helps, and using it against the wrong person can actually hurt – both the individual, and science as an enterprise.
As a young but very real scientist, I met MANY emerging young crackpots, who considered me a potential sounding board – and I like to think that I converted most of them to either outright scientists, or scientifically literate aficionados of real science. In fact, I don’t recall ANY junior crackpots who I could not make more logical and scientific by patience, understanding, and teaching of the sublime joys of REAL understanding and discovery.
More than that, was the GOOD that crackpots did for me. By patiently trying to understand what crackpots were saying, I invariably walked away a better scientist. Errors don’t just force you to ask ONE right question – they force you to ask MANY excellent questions. Sometimes it requires the patience of Job, but that’s just one more reason why reading my Bible has been so helpful.
Crackpottery, analyzed deeply, always leads back to real science, often including things I didn’t know, or didn’t know well enough. Most crackpot science is – in my experience, one of three things: (1) some very illustrative, useful, and “teachable” error, or (2) some well-known and very beautiful aspect of science or mathematics, which seems novel, but isn’t, or (3) some kind of “old science” which is very intuitive, but is now understood to be wrong.
Of course, there can be many layers of JUNK on top of the key scientific mistake, as the crackpot uses even more crackpot ideas to hold everything together, as the key idea fails. However, I would not want to laugh too loudly about such a dubious tactic, as “Bondo and paint” are also used very effectively in real science, politics, and law.
Sometimes, when discussing crackpottery in science, I like to say this.
“There is a potential scientist in every crackpot, and a potential crackpot in every scientist.”
I find that crackpot ideas are a great introduction to a conversation about real science. The trick is turning the exuberant crackpot away from the dopaminergic lust of superficial logical connections – and getting them addicted to the patient romance of deep conceptual relationships and understanding. If the latter reminds you of real love – Biblical, academic, humanitarian, or philosophical – you are absolutely right. I believe it is our duty, as people who LOVE science and math, to elevate crackpots from their trap, even if we fail, but in the process, to “teach to the fourth wall”. And that is exactly what I’m doing now.
The hot pants of OMG / string of buzzwords / “maybe this stuff is all related and I can see it” is the addictive pseudoscientific experience that crackpots cannot get out of their minds. But let them experience a “fellow scientist” showing them that they are TRULY CORRECT about something that they said, and how this idea was explored by famous scientists in history, and you can begin the process of instilling the DISCIPLINE that the crackpot so sorely needs.
Reforming a crackpot can take days, weeks, months or years. The key is to nurture the healthy joys that come from disciplined understanding, as a substitute for the toxic buzz of loose conjecture rooted in loose quasi-understanding.
Some crackpots are beyond help, and scientists who are teaching to more open minds (think about our own SteveInCO) cannot afford to waste their time on those few minds that will never attain self-skepticism within this lifetime. Walking away from crackpots who have very intentionally broken and super-glued the keys of reason in the corresponding locks, is simply necessary.
I get this. For all my criticisms of Neil deGrasse Tyson, and scientific disagreements with him, I completely understand his need to tell Terrence Howard to “move along, thank you” and to stop listening to the nonsensical ideas of Terryology.
Note that Joe Rogan does NOT get this, and he will need to be gently schooled on this point. I admire that Joe will listen to Terrence, but Joe is also a bit too easily swept up into Terrence’s world of delusional mumbo-jumbo.
Terrence Howard and Terryology are where we begin this discussion.
To be brief, Terrence was known more as an actor than as a pseudoscientist, but when he appeared on the Joe Rogan Experience, he exploded into the national consciousness. I am including the entire 3-hour interview, but I strongly caution against watching the whole thing without having some of the context I’m going to provide. On the other hand, a few random clicks will give you the flavor in a most enlightening way.
Terrence Howard – Full Interview on The Joe Rogan Experience
Terrence Howard is clearly a nice guy, and I am certain that I could be his friend. We might even have some profound discussions about the periodic table, as he comes very close to real science there, and THAT is where I would strike to try to reform him (see sidebar in Appendix). However, he is unlikely to ever gain the discipline of self-skepticism, to temper his equally welcome skepticism of scientific orthodoxy. The best that can be done, is to use him as a living example of an important dysfunction in science, and to educate the masses by reacting to him.
Surprisingly, that works really well, and that’s why I’m here.
Terrence is (in my humble opinion) a living example of the idea that a little bit of knowledge can be a dangerous thing.
Terrence is an actor, but before that, he ALMOST became a scientist – specifically, a chemical engineer. However, at the exact moment when accepting some discipline from his teacher would have helped him become a true scientist, he rejected the teaching, and dropped out of school.
To get to the heart of that break, Terrence believes that, because 2 times 2 equals 4, 1 times 1 should equal 2. Now, I will admit that the feeling that something should be different is extremely useful in scientific discovery, but we also know from experience that should is extremely dangerous in almost any context. Psychologists routinely repair people by getting them to understand that their list of shoulds has grown too long and nonsensical to be mentally and physically healthy.
Terrence claims that the issue of this mathematical argument is why he dropped out of college – that his teacher could not accept this new form of math, which is part of what Terrence calls Terryology.
I have no idea if that account is true, or the full story, and I strongly suspect that Terrence was having more trouble than just a disagreement with his teacher over math. There is even some doubt that Terrence was ever in college, but let’s just set that aside, and assume that Terrence did start to attend college. It is very likely that Terrence had a bad understanding of math at very basic levels, and was not able to follow the teachers in his classes, due to that faulty understanding. However, in the hubris of academic freedom, which new students often experience, I suspect that Terrence basically went off the rails. Here is a teacher talking about his theory of Terrence’s defective education.
Many people think that Terrence is conflating addition (where 1+1=2 and 2+2=4 are true) with multiplication. I have my own theory – that Terrence is simply intuiting a new operation – unfortunately rather ill-defined – which is basically y=2x but poorly expressed as y=x*x or y=x^2 (y equals x squared).
And once I realized this, I noted something else.
If you ever had any differential (first semester) calculus, you may have noted that y=2x is – more or less – the first derivative of y=x^2 (y equals x squared).
This video explains what that means.
My explanation of Terrence’s idea would then be that the thing that should be 2 at 1, but is also 4 at 2, is in fact the derivative of self-multiplication – not self-multiplication itself.
I’m definitely NOT saying that Terrence Howard “re-invented calculus”, but what I am saying is that his “invention” – in a very typical crackpot way – is in fact a personal rediscovery of something real, known, and actually very beautiful – and THAT is part of the seduction of crackpottery. Terrence is able to see it, but he doesn’t have the patience and rigor to realize what he’s intuiting, nor the language to communicate it. He TRIES to communicate it, but he fails to use the language others have agreed to use. He uses new terms – neologisms – and people almost get it, in a similar way. As Terrence piles on more analogies and scientific verbiage, people nod and make sounds of insight, but nobody really, truly, understands.
Normal people having beautiful mathematical realizations is not uncommon. Moreover, these realizations are sometimes hard to put into words. Thus, these ideas may seem novel and inventive – and they are in fact novel to the person thinking them, and they were likely inventive, to at least some extent (unless they were just badly remembered math lessons). But the idea that this new thought is a NEW INVENTION TO THE WORLD is a huge leap that is almost never true.
The aforementioned near-tangibility of crackpot ideas, and the communicability of that near-tangibility, are part of the danger of crackpottery – the fact that others “kinda get it” just like Terrence does. This crackpot virality spreads a sort of vague almost-thinking which reminds me of the feckless and far-too-innocent Eloi in H.G. Wells story of The Time Machine.
However, don’t expect me to push for “Big Sister” and her net nanny censors to crack down on crackpots. Instead, we need more people to understand math, and to see the beauty in things like y=x^2 and its derivatives.
Biology – same thing. Remember – the vague “almost tangible idea” that men can be women if we all believe they are, is another great example of a viral crackpot idea – in this case, one that the current government endorses.
Trans women are real – they just aren’t truly women, even if we all try to believe that they are. I’m not calling for censorship of that idea, either. I’m calling for no censorship on the questioning of it, just like I would call for no censorship on Terrence Howard’s ideas, nor on the criticism of his ideas.
If you have already been somewhat seduced by Terrence Howard, you really need to listen to some of his critics. That said, I recommend an attitude of love and sympathy – even when you feel frustrated and annoyed. See if you can “do better” than these two critics, in terms of sharing their ability to be skeptical of what is obviously wrong, and remaining firm in your resistance to “feeling” the truth of what Terrence is saying, while still maintaining open-mindedness, and a desire to “make Terrence make sense” – but without compromising your skepticism.
What is the key difference between scientists like me and Steve, and pseudoscientists like Terrence?
Speaking for myself, the difference for me, is that I test and beat up my crackpot ideas, so in almost all cases where my “brilliant” idea isn’t simply WRONG, I discover that I’ve rediscovered something beautiful. Very few of my crackpot ideas have value, and most of those end up being hypotheses and conjectures that are not only limited, but need more work.
In my opinion, you’re not a true scientist unless you’ve rejected literally hundreds or thousands of your own ideas – refining just a few of the survivors into something that might have some limited value.
Self-skepticism is necessary. Enough to tame crackpot ideas, but not so much as to stifle innovative thinking.
What is the difference between, say, Robert Malone, who I deeply respect as a scientist, and Terrence Howard?
In a nutshell, Malone has been skeptical of his own ideas – and at a level which required extreme honesty and moral courage. His willingness to admit that his own technological children – mRNA therapeutics and vaccines – have problems and still need work, is just mensch level eleven. Time after time, Malone sees though the bullshit of a scientific orthodoxy which has cowered before self-interest, money, and power.
Malone, like many who question the current media-and-government-driven “new consensus” in vaccine and therapeutic science, points out the hypocrisy of the sudden new orthodoxy, relative to many of its backers’ own well-established principles of ethics and morality. Examples include the Hippocratic oath, “first do no harm”, patient rights, medical privacy and freedom, and a host of other ideas which were unassailable, just a few years ago. In essence, Malone calls upon the orthodoxy to live up to its own ideals, not in the Satanic Alinsky way that actually hates and despises those ideals, but in a Godly way that deeply loves and respects those ideals.
Crackpots, in contrast, tend to reject the orthodoxy in a dismissive way, without respecting any, or most, of its underlying and fundamental tenets. They almost always fail to explain what’s wrong with the consensus view, or the underlying principles. They dismiss it without adequate explanation. In fact, crackpots who disrespect Einstein without actually doing the hard work of understanding Einstein first, are so pervasive that disrespect of Einstein is almost diagnostic for crackpottery.
Although spotting and pointing out crackpot thinking is important, it is also important for us to push back, when the crackpot term is applied unfairly to people who are simply not crackpots.
Robert Malone, who my friends and I admire, is an obvious example to us of somebody who is not a crackpot, but Neil deGrasse Tyson and Peter Hotez, who we disagree with and don’t like, are also not crackpots, if we are honest. Neil and Peter and their ilk may have other problems, including extreme bias, corruption, and compromise by unethical government involvements, but they are not crackpots.
Even when they look and sound like crackpots!
Now, there are thousands if not millions of true crackpots, most of whom labor in obscurity, and I can’t show them all, but I would be remiss not to include at least one, a man named Roger Spurr, whose awful theories have been discussed on this site very much in the last few days.
Note the disrespect for Einstein – this is very typical.
If you can’t abide listening to his very vague and loose reasoning in the video, try this website, where you can read it instead. For me, that’s easier.
Now, to be completely honest, I (and everybody else with any significant background in physics) have my own “crackpot” speculations on what may be right or wrong with the Standard Model of particle physics, as well as the top competitors for extending or replacing it. My personal crackpottery includes disrespect for supersymmetry, and massive side-eye on what I would call “irrational exuberance by the mainstream in regard to dark matter.” Nevertheless, I am always eager to test those thoughts, trash those thoughts, or modify those thoughts, based on the latest experimental results. Indeed, when the definitive experiments come in, supporting either supersymmetry or dark matter, I will be converted by them – as I should be. What I can say with certainty about Spurr’s reasoning, is that I would have thrown out nearly all of his thoughts long ago, based on the huge quantities of very solid and very basic evidence against them.
In many ways – like the term used by Wolfgang Pauli, that became (fairly or unfairly) the title of a book criticizing the non-productivity of string theory – Spurr is not even wrong.
So what is the path forward?
How do we deal with “bad science” – pseudoscience – crackpot theories – whatever you want to call them?
The Founding Fathers had a very excellent idea with Free Speech.
It is my belief that the ultimate protection against crackpottery is free speech. As long as we can criticize not only the orthodoxy, but the ideas of our fellow critics, then everything is subject to healthy sunlight. When secrecy is used to protect ideas from challenge, or government uses its punitive powers to protect its own very open crackpottery, bad things happen.
To quote a certain blog, quoting a certain scientist:
“We do not believe any group of men adequate enough or wise enough to operate without scrutiny or without criticism. We know that the only way to avoid error is to detect it, that the only way to detect it is to be free to inquire. We know that in secrecy error undetected will flourish and subvert.”
J. Robert Oppenheimer
I’m good with sunlight, as a way to help us find truth. And I hope you are, too.
One place where Terrence Howard comes very close to actual innovative thinking is in his personal interpretation of the periodic table of the elements. This, despite many, many problems.
Terrence’s thinking about the elements is still (IMO) rather crackpot, and although his view of the table in terms of frequencies seems fascinating, it’s truly unnecessary, as his critics point out. Terrence’s few predictions are also quite wrong. Thus, his very different viewpoint is not clearly any BETTER than any other view of the elements, when gauged by the very basic metric of prediction generation. What Terrence is saying simply doesn’t appear to be useful.
HOWEVER, Terrence does come up with a very nice concept, which is hidden by his crackpot terminology, and almost lost by his inability to create a truly marketable neologism for it.
I happen to be good at neologisms, so I’ll do it for him.
As I’m watching Terrence, I am quite certain that he has “rediscovered” or “repackaged” some well-known concepts which are an important part of freshman chemistry. In particular, the concepts of electronegativity and electropositivity, which are powerful ideas about how different elements behave due to their electronics, seem to be things he’s describing.
Even more, if we accept that Terrence has rediscovered electronegativity and electropositivity, then he also seems to be proposing a very nice idea which bridges those two concepts, and which is frankly very needed, that idea being what I might call, more marketably, electroneutrality.
This is not Earth-shattering, but it’s nice.
So let me just be very clear. In a crackpot way, using bad terminology, making bad predictions, and wrapping it all in an unnecessary “musical” paradigm which most people don’t find useful at all, Terrence has still pushed a rather innovative idea – that highly “electroneutral” elements like carbon are a special thing we need to talk about in that context.
None of that is anything that my freshman chemistry professor didn’t say in different, more conventional ways. That’s exactly how I spotted it in Terrence’s ramblings. But bear in mind – that man was a true genius – with a photographic memory. He was a highly awarded and esteemed scientist, who worked on the Manhattan Project and many other such things. He was a rock star at the university. Students fought with each other and with the campus bureaucrats to get into his classes.
And while that great educator came close, but didn’t quite do it, Terrence straight-up pinpointed the fact that a curve inflection (think second derivative!) located between electronegativity and electropositivity is actually something worth conceptualizing, appreciating, and TEACHING.
I can imagine Terrence in my college chemistry class, taking that idea up to my professor, and that wonderful man not only listening and understanding through the broken terminology, but doing a complete lecture to us on what Terrence had just told him, or using it to create a test question, which he often did when somebody said something he found to be profound. I can see that same professor pushing the idea in chemical education – maybe even writing a paper on the concept. And in doing so, he would have demonstrated discipline to Terrence, showing him the true value of his thinking, and helped him to become an honest-to-God scientist.
I’m not certain if Terrence’s musical and frequency viewpoints have any real value in chemistry, but I do find them fascinating for both scientific and artistic reasons. Beyond that, the reason I don’t dismiss the possibility outright, is that Terrence put his finger on the undervaluing of electroneutrality in chemistry, using his bizarre methodology. So the fact that he came up with a worthwhile thought using it, may say something for the methodology used, especially if the latter could be cleaned up and made practical. I would bet against it, but not so much that I might not actually try to fully understand his frequency methodology at some point.
Like I said earlier, I have always gained something by trying to understand crackpots. Because, as I said, in every crackpot, there is a real scientist trying to get out and say something.
In closing, I’d like to thank Brave and Free for bringing the above video, which started all of this discussion. That is precisely why we’re here, practicing Free Speech – so that we can all learn something!
This Stormwatch Monday Open Thread remains open – VERY OPEN – a place for everybody to post whatever they feel they would like to tell the White Hats, and the rest of the MAGA/KAG/KMAG world (with KMAG being a bit of both).
Please forgive us, Wheatie, we did not know That you had left us with armor in tow We had no idea with what you dealt We did not know the pain you felt And now we can only imagine With you what really did happen Cause rarely did you complain And/or share your personal pain Of one thing we are most certain You are flying high behind the curtain Watching over us above the crowds Our Warrior Angel above the clouds Thank You, Wheatie, for caring for us While you were here among the fuss We miss you dear you have no idea Since time began in the pangaea With you there was no time In your wisdom you would chime To clarify and magnify The what where how and why We did not question when you left We were not slightly bereft But over time we wondered why You did not at least stop by Now we know where you have gone With the break of this new dawn We could be angry but are not Tho with an arrow we’ve been shot Rest peacefully Warrior Angel dear Send us a sign that you are near A butterfly a flower a kiss of rain From your love do not refrain God sends Angels to watch over us And now we have an Angel Plus A Warrior Angel of Magnificence From today and forward hence
Boilerplate, more or less, but worth reading again and again, if only for the minor changes, and to stay out of moderation.
MINOR CHANGE NUMBER 1
Never talk about committing violence in a reply to Wolf or in response to anything Wolf has said, or you may get put into moderation so that your comments can be screened. This is ONLY because DHS is now playing door-knock Gestapo with people who have spoken at school board meetings, made public comments, etc. DHS regime jackboots are knocking on doors of school board mama bears and stupidly insinuating potential violence from things people say or don’t say on social media. A guy in Ohio pointed his FINGER at the school board, and they went after him, armed with pictures of the pointing, and screen captures of online comments. Yeah.
SO – give the Nazis ZERO ammo. Keep any mention of violence, even joking, away from Wolf, so that he doesn’t have to “explain” humor to humorless jackboots who pretend not to know things.
As for discussion of “violent humor” among yourselves (e.g., “#TeamHeadsOnPikes”), just use whatever discretion you think is appropriate for yourselves. I will only put you in moderation if your comments create problems for ME or THIS SITE, but not if they only impact you.
YOU are responsible for your own comments, if they come knocking. YOUR choice. Just remember this…..
OTHER THAN THAT…….
The bottom line is Free Speech. Theories and ideas you don’t agree with must be WELCOME here, and you must be part of that welcoming. But you do NOT need to be part of any agreement.
Bottom line – respect other people’s FIRST AMENDMENT RIGHTS.
Our only additional requirement is that you do so NICELY. Or at least try to make some effort in that direction.
SO….. [ENGAGE BOILERPLATE…..]
We must endeavor to persevere to love our frenemies – even here.
Those who cannot deal with this easy requirement will be forced to jump the hoops of moderation, so that specific comments impugning other posters and violating the minimal rules can be sorted out and tossed in the trash.
In Wheatie’s words, “We’re on the same side here so let’s not engage in friendly fire.”
That includes the life skill of just ignoring certain other posters.
We do have a site – The U Tree – where civility is not a requirement. Interestingly, people don’t really go there much. Nevertheless, if you find yourself in an “argument” that can’t really stay civil, please feel free to “take it to the U Tree”. The U Tree is also a good place to report any technical difficulties, if you’re unable to report them here. Please post your comment there on one of Wolf’s posts, or in reply to one of Wolf’s comments, to make sure he sees it (though it may take a few hours).
We also have a backup site, called The Q Tree as well, which is really The Q Tree 579486807. You might call it “Second Tree”. The URL for that site is https://theqtree579486807.wordpress.com/. If this site (theqtree.com) ever goes down, please reassemble at the Second Tree.
If the Second Tree goes down, please go to The U Tree, or to our Gab Group, which is located at https://gab.com/groups/4178.
We also have some “old rules” and important guidelines, outlined here, in a very early post, on our first New Year’s Day, in 2019. The main point is not to make violent threats against people, which then have to be taken seriously by law enforcement, and which can be used as a PRETEXT by enemies of this site.
In the words of Wheatie, “Let’s not give the odious Internet Censors a reason to shut down this precious haven that Wolf has created for us.”
A Moment of Prayer
Our policy on extreme religious freedom on this site is discussed HERE. Please feel free to pray and praise God anytime and anywhere.
Thus, please pray for our real President, the one who actually won the election.
You may also pray for our nation, our world, and even our enemies.
Musical Interlude
In honor of dear Wheatie, we now present some music to soothe, inspire, invigorate, or relax.
Our beloved country is under Occupation by hostile forces.
Daily outrage and epic phuckery abound.
Don’t let UFOs and Chinese spy balloons distract you from the fact a US President ordered Russian pipelines be blown up without notifying Congress then misled the American people about it, risking WWIII to defend a corrupt nation where his son Hunter raked in millions of dollars
And we will keep saying Joe Biden didn’t win until we get His Fraudulency out of our White House.
Wolfie’s Wheatie’s Word of the DayYear Week:
CRISPR
noun
Clustered Regularly-Interspaced Short Palindromic Repeats
A naturally occurring mechanism found in bacteria that involves the retention of fragments of foreign DNA, providing the bacteria with some immunity to viruses. The system is sometimes referred to as CRISPR/Cas9 to denote the entire gene-editing platform in which RNA homologous with the targeted gene is combined with Cas9 (CRISPR Associated Protein 9), which is a DNA-cutting enzyme (nuclease) to form the “toolkit” for the CRISPR/Cas9 method of genome editing.
Wolf’s explanation: ZoneAlarm / McAfee for bacterial genes against IRL viruses. The bacteria keep a special library of virus crap, then look for it in the genome and “quarantine” (slice) any infected DNA at the bad spot.
Cas9
noun
CRISPR Associated Protein 9
A specialized enzyme known as a nuclease that has the ability to cut DNA sequences. Cas9 makes up part of the “toolkit” for the CRISPR/Cas9 method of genome editing.
A high-level explanation of how CRISPR/Cas9 works (EASY):
A Very Geeky Technical Explanation of CRISPR/Cas9 in Indian English (HARD):
WEF-Invited Talk by a Discoverer of CRISPR/Cas9 Five Years Before She Got a Nobel Prize (EASY):
Guardian Happy Video One Year Before (Be Sure to Note Hitler Dream) (EASY):
Nobel Prize Lecture by Jennifer Doudna (Includes an Excellent Visual Explanation of CRISPR/Cas9 Technology) (MEDIUM):
TL;DR – The spike protein not only contains a special sequence that allows it into the cell nucleus – it also has an ability to bring its own spike mRNA sequence with it. Both features appear to be unique among coronaviruses. The features explain genomic incorporation found for both the virus and the vaccines. The special key and the mRNA shepherding can be considered to be defects in any spike vaccine that has them.
Also, NONE of the “bigs” are talking about this, but it is HUGE, if only people will read the paper.
By sheer luck, I was alerted to this new development ASAP on Twitter.
A follower of mine, who I had followed back, posted on Twitter the link to a paper with this title:
Nuclear translocation of spike mRNA and protein is a novel feature of SARS-CoV-2
I immediately realized what this was about.
It’s about how the SARS-CoV-2 (COVID) virus spike protein and its mRNA get into the cell nucleus – an extremely important point which WSB has been hitting on over and over. It’s very important, because THAT is how “genomic incorporation” happens. And genomic incorporation is what HIV does – what retroviruses do. They “get into” the DNA and leave cookies, so to speak.
Sometimes, they leave enough cookies, that the whole virus comes back out, fully functional, and ready to infect. Sometimes, they only leave enough junk in the DNA to cause some damage. Sometimes, they leave enough to change us – and that is why human DNA is filled with “viral leftovers”.
In principle, mRNA technology should NOT do this. We were TOLD that mRNA technology could not do this. But somebody LIED TO US. And not only that – NOBODY – from Bill Gates on down – ever apologized to us about lying, or even about just “being mistaken”.
We’ll get to that later.
You will recall that there are two papers I love to mention.
One is the “Jaenisch paper”, which describes how the SARS-CoV-2 virus manages to get some of its genetic instructions for the spike protein into the DNA of cells.
The other is the “De Marinis paper”, which describes how the Pfizer vaccine did the same thing to human liver cells in vitro – meaning that in an experiment using cells in culture, the Pfizer vaccine got its mRNA sequences into the DNA genetic material of human liver cells, and it did so in a matter of minutes.
McCullough got in a lot of trouble with Twitter for posting this, even though it was utterly true. Now we know that the government was trying to shut it down. They likely used the technicality of McCullough’s very VALID speculation (stated as speculation and concern), which turned out to be correct, IMSO.
These papers explain ALMOST everything. When I saw the Jaenisch paper, I predicted that we would see the De Marinis paper. MEANING – when I saw that the virus could get mRNA into the DNA, I predicted that the vaccine might get its mRNA into the DNA, too. And yes, I was right. Clearly others thought the same thing, and decided to investigate.
Now, after the De Marinis paper, it seemed very obvious to me that one did not need any kind of special conditions or reverse transcription promoters to get the vaccine mRNA to incorporate.
That bothered me, and I suspected, at the time, that MAYBE – just maybe – the spike protein ITSELF was somehow causing genomic incorporation – that it functioned as a kind of reverse transcription promoter.
Well, it sure looks like that is the case.
According to the discoveries revealed in the new paper, which I have taken to calling the “Mehedi paper”, there is a special sequence in the spike protein that acts like a “key to the nucleus” – and this sequence is found in NO other coronavirus spike protein.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes severe pathophysiology in vulnerable older populations and appears to be highly pathogenic and more transmissible than other coronaviruses. The spike (S) protein appears to be a major pathogenic factor that contributes to the unique pathogenesis of SARS-CoV-2. Although the S protein is a surface transmembrane type 1 glycoprotein, it has been predicted to be translocated into the nucleus due to the novel nuclear localization signal (NLS) “PRRARSV,” which is absent from the S protein of other coronaviruses. Indeed, S proteins translocate into the nucleus in SARS-CoV-2-infected cells. S mRNAs also translocate into the nucleus. S mRNA colocalizes with S protein, aiding the nuclear translocation of S mRNA. While nuclear translocation of nucleoprotein (N) has been shown in many coronaviruses, the nuclear translocation of both S mRNA and S protein reveals a novel feature of SARS-CoV-2.
Let me put that in plainer English.
COVID-19 really hurts old people and seems to be both deadlier and easier to catch than other coronaviruses. The spike protein seems to be why. Although the spike protein is a surface protein that normally would not do this, it might be predicted to get into the cell nucleus because it has a special sequence “PRRARSV,” a known key to the nucleus which appears in no other coronavirus. Sure enough, the COVID spike protein gets into the nucleus of infected cells. What’s more, the mRNA for COVID spike protein also gets into the nucleus. What happens is that the spike mRNA collects near the spike protein, which helps it get in. While a different protein called the “nucleoprotein” of many coronaviruses is known to get into the nucleus of cells, the penetration of the cell nucleus by BOTH the spike protein AND the mRNA for it, seems to be a unique new feature of the SARS-CoV-2 virus.
Once you read it in plain English, it’s much more mind-blowing.
Now – I really recommend that you read the rest of the paper, but it’s really just technical details about what was mentioned in the abstract. Those details can help you gauge the expectedness or unexpectedness of things, but I have tried to do that as best as I could in the translation.
At this point, you should have all kinds of questions.
could this defect of the vaccines have been predicted?
should it have been predicted?
did the Chinese know this when they sent us the sequence?
did we know it when we got the sequence?
would NOT using the full spike protein have prevented this?
if so, why did we use the full spike protein anyway?
would the “forbidden” Winfried Stöcker RBD vaccine have avoided this?
if so, why was his vaccine suppressed by the German government?
does this affect the Peter Hotez vaccine, Corbevax?
if not, why didn’t his vaccine get promoted through the process quicker?
is nuclear penetration a common problem with mRNA technology?
how did this “key” get into the sequence? Naturally or not?
could “directed evolution” of the spike have yielded this?
why wasn’t this clear from the moment we got the sequence?
did people know this and hide the information?
were key people like Bill Gates (their side) and Robert Malone (our side) aware of this possibility?
The last question is a gift to WSB and her virologist friend. I am by default a defender of Dr. Malone, but WSB and her friend are long-time skeptics of the technology, and thus of Dr. Malone. In all fairness, I think we have to ask EVERYBODY the same questions.
Did people KNOW that mRNA technology had this vulnerability?
Does this look any more like an engineered bioweapon, designed to get into the nucleus?
Was this thing made by nature, by people, or by somebody with more advanced technology?
What is the purpose of getting into the nucleus, if it is designed to do that?
That should be enough. I will leave some links to prior comments I have made, in an appendix, hopefully added later.
Thank you.
W
John Fink and James Coburn discuss case in a scene from the film ‘The Carey Treatment’, 1972. (Photo by Metro-Goldwyn-Mayer/Getty Images)
BUT WAIT! The depop shot doesn’t just work on the euthanasia end of things…..
See, for example, what I was thinking BEFORE the Pfizer data showed us that the VACCINE was migrating – i.e, back when I thought it was ONLY the spike protein itself that was migrating.
Yeah. Funny about that spike protein. Funny how Dr. Malone tried to warn NIH and FDA that the spike protein was way too pathogenic to be used as an immunogen, and they just said “we’re good”. (Y’all can research this one yourselves. Look through multiple Malone interviews to find a nice, long, complete account of it.)
It’s taken us a while for this to be generally recognized, but I think we’re there now.
“The spike protein is probably one of the most toxic proteins the human body has ever seen.”
Dr. Paul Marik explains the dangers of a buildup of spike protein in the body, from inflammation to autoimmune disease.
The answers in the above Twitter video are not as “scientifically complete and direct” as I would have answered, and I actually have some minor scientific quibbles, but overall, this is 99% correct, and completely correct on the outrageous pathogenicity of the spike protein.
Especially the Wuhan-sequence spike protein that they STILL include in the shots, for absolutely no scientifically valid reason.
Yeah, think about that. GODDAMN depoppers.
I have to say, the fact that I came to the same conclusion as Malone about the spike protein a long time ago, but after he did, for completely different reasons, backs the idea that this could have been, should have been, and probably WAS obvious to somebody else.
Using Principles of Protein Equivalence and Analogy as Predictive Tools for Coronavirus Understanding Surely you’ve heard of the BROWN RECLUSE SPIDER. The brown recluse is related to several other recluses, and a couple of other families of spiders, that all have a similar venom – a protein called sphingomyelinase D. This is an enzyme that …
TL;DR – you MUST listen to a short podcast of a scientist revealing the latest research on the spike protein vaccines. The VACCINE ITSELF (not just the spike protein – the mRNA vaccine itself) is persistent and is not only concentrating in ovaries – THE VACCINE ITSELF IS EXCRETED – e.g., in breast milk. Meaning …
As a young science student in the 1970s, I never would have thought that I would have to correct the American and global media over an issue of late 19th century basic science, but yet, here we are. When basic theories of MATTER and CHEMISTRY proved that “Compound A created by one route has the …
Which just makes the idea that some people WANTED this to happen, all the more likely.
What if I could explain every head-scratcher of the “pandemic” with a simple idea – that vaccination is the ideal format for introducing real, workable, tunable, and long-running “population control” into socialized medicine without anybody really noticing or caring? Intro to the Intro It’s one of those things that – once you see it – …
Bottom line – people are recognizing vaccine-related depop as a REALITY.
Time to make them self-reflect upon what they’re doing, pushing these bad vaccines.
NOTE: At the moment, “depop.gov” is not a real site – it’s a “parody hypothetical URL”. I have no idea if anything is parked there. What happens after this is not my doing, and the parody URL stands as what was intended. Parody. But deadly serious parody. It’s time to wake the HELL up, world.
Get your rest, Trumpy Bear! You’re going back to the White House!!!
We can’t let SNIFFY BEAR destroy it any more than we already have!!!
The Business At Hand
This Stormwatch Monday Open Thread remains open – VERY OPEN – a place for everybody to post whatever they feel they would like to tell the White Hats, and the rest of the MAGA/KAG/KMAG world (with KMAG being a bit of both).
And indeed, it’s Monday…again.
But we are COOL WITH IT.
The Rules
Boilerplate, more or less, but worth reading again and again, if only for the minor changes, and to stay out of moderation.
The bottom line is Free Speech. Theories and ideas you don’t agree with must be WELCOME here, and you must be part of that welcoming. But you do NOT need to be part of any agreement.
SO….. [ENGAGE BOILERPLATE…..]
We must endeavor to persevere to love our frenemies – even here.
Those who cannot deal with this easy requirement will be forced to jump the hoops of moderation, so that specific comments impugning other posters and violating the minimal rules can be sorted out and tossed in the trash.
In Wheatie’s words, “We’re on the same side here so let’s not engage in friendly fire.”
That includes the life skill of just ignoring certain other posters.
We do have a site – The U Tree – where civility is not a requirement. Interestingly, people don’t really go there much. Nevertheless, if you find yourself in an “argument” that can’t really stay civil, please feel free to “take it to the U Tree”. The U Tree is also a good place to report any technical difficulties, if you’re unable to report them here. Please post your comment there on one of Wolf’s posts, or in reply to one of Wolf’s comments, to make sure he sees it (though it may take a few hours).
We also have a backup site, called The Q Tree as well, which is really The Q Tree 579486807. You might call it “Second Tree”. The URL for that site is https://theqtree579486807.wordpress.com/. If this site (theqtree.com) ever goes down, please reassemble at the Second Tree.
If the Second Tree goes down, please go to The U Tree, or to our Gab Group, which is located at https://gab.com/groups/4178.
We also have some “old rules” and important guidelines, outlined here, in a very early post, on our first New Year’s Day, in 2019. The main point is not to make violent threats against people, which then have to be taken seriously by law enforcement, and which can be used as a PRETEXT by enemies of this site.
In the words of Wheatie, “Let’s not give the odious Internet Censors a reason to shut down this precious haven that Wolf has created for us.”
A Moment of Prayer
Our policy on extreme religious freedom on this site is discussed HERE. Please feel free to pray and praise God anytime and anywhere.
Thus, please pray for our real President, the one who actually won the election.
Prayers for your enemies, and your enemy’s enemies, and your enemy’s enemy’s enemies, are all permissible.
MUSICAL INTERLUDE
For your listening enjoyment, and general encouragement, we continue Wheatie’s tradition of fine music videos, shipped fresh from the seas of information by our intrepid authors.
While looking at videos in an earlier week, I accidentally discovered this oddball American sister duo on the Latin “pop country whatever” music charts.
…..and later realized that such a sister act is not a totally unique thing…..
…..although it certainly looks like BOY DUOS are more common…..
Q’s post addressed to Nate Cain (qanon.pub post 2578) had a line which really struck a nerve: YOU ARE NEVER ALONE. Here is the post. Q !!mG7VJxZNCI ID: 52a4e6 No.4250950 Dec 10 2018 23:13:47 (EST)https://twitter.com/cain_nate/status/1072221511443013633Sometimes ‘intrusions’ have a way of safeguarding people & evidence.Sometimes ‘intrusions’ are a necessary event in order to safeguard chain of custody [post OIG WB status …
…..and while I was looking for that Elenyi video, I found this, but it’s not a duo…..
…..and that kinda balances out the Barlow Girl trio.
“And so it goes.”
Call To Battle
Actors Henry Fonda and James Coburn on the set of Universal Studios movie ” Midway” in 1976. (Photo by Michael Ochs Archives/Getty Images)
Our beloved country is under Occupation by hostile forces.
Daily outrage and epic phuckery abound.
…..and then…..
We can give in to despair…or we can be defiant and fight back in any way that we can.
If you want to download the Pfizer documents – the ones that they wanted to hide for 75 years or whatever – it’s easy. But first, a couple of videos to set things up a bit.
Now it’s really a one-page site – they get right down to business on the landing page…..
You can search through the site to select documents first, OR you can just download to your heart’s content. Here is the bottom of the page, with nothing selected, so the download button is grayed out.
Now, if you want to download ALL of the documents just go to that drop-down button in the lower left corner…..
…..and change the setting from “Show [ 25 ] per page” to “All”. Then, you will get a single page, and you can put a checkmark on ALL 150 documents (which is tedious as hell, but it works).
When you download all of these documents, they will come in a ZIP file. You can then extract all of the documents out of the zip file, and then view each of them with the proper application.
Enjoy!
Wolfie’s Wheatie’s Word of the Day:
endeavor
noun
A conscientious or concerted effort toward an end; an earnest attempt.
Purposeful or industrious activity; enterprise.
verb
To exert oneself to do or effect something; make an effort; strive.
To attempt; try.
Used in a quote:
We thought about it for a long time, “Endeavor to persevere.” And when we had thought about it long enough, we declared war on the Union.
Hang in there, Trumpy Bear! You’re going back to the White House!!!
No more of this Sleepy Creepy guy, provoking needless wars to fill Democrat coffers!
The Business At Hand
This Stormwatch Monday Open Thread remains open – VERY OPEN – a place for everybody to post whatever they feel they would like to tell the White Hats, and the rest of the MAGA/KAG/KMAG world (with KMAG being a bit of both).
And indeed, it’s Monday…again.
But we WILL get THROUGH IT, OVER IT, and BEYOND IT.
The Rules
Boilerplate, more or less, but worth reading again and again, if only for the minor changes, and to stay out of moderation.
The bottom line is Free Speech. Theories and ideas you don’t agree with must be WELCOME here, and you must be part of that welcoming. But you do NOT need to be part of any agreement.
In an image…….
Try to make it real.
SO….. [ENGAGE BOILERPLATE…..]
We must endeavor to persevere to love our frenemies – even here.
Those who cannot deal with this easy requirement will be forced to jump the hoops of moderation, so that specific comments impugning other posters and violating the minimal rules can be sorted out and tossed in the trash.
In Wheatie’s words, “We’re on the same side here so let’s not engage in friendly fire.”
That includes the life skill of just ignoring certain other posters.
We do have a site – The U Tree – where civility is not a requirement. Interestingly, people don’t really go there much. Nevertheless, if you find yourself in an “argument” that can’t really stay civil, please feel free to “take it to the U Tree”. The U Tree is also a good place to report any technical difficulties, if you’re unable to report them here. Please post your comment there on one of Wolf’s posts, or in reply to one of Wolf’s comments, to make sure he sees it (though it may take a few hours).
We also have a backup site, called The Q Tree as well, which is really The Q Tree 579486807. You might call it “Second Tree”. The URL for that site is https://theqtree579486807.wordpress.com/. If this site (theqtree.com) ever goes down, please reassemble at the Second Tree.
If the Second Tree goes down, please go to The U Tree, or to our Gab Group, which is located at https://gab.com/groups/4178.
We also have some “old rules” and important guidelines, outlined here, in a very early post, on our first New Year’s Day, in 2019. The main point is not to make violent threats against people, which then have to be taken seriously by law enforcement, and which can be used as a PRETEXT by enemies of this site.
In the words of Wheatie, “Let’s not give the odious Internet Censors a reason to shut down this precious haven that Wolf has created for us.”
A Moment of Prayer
Our policy on extreme religious freedom on this site is discussed HERE. Please feel free to pray and praise God anytime and anywhere.
Thus, please pray for our real President, the one who actually won the election.
You may also pray for our enemies, many of whom were grievously harmed by their foolish choice to virtue signal with the experimental gene therapy vaccines, which were snuck upon all of us by the monstrous WEF, Pfizer and Moderna, despite our warnings, and because this corrupt administration, media, and social media suppressed the truth.
MUSICAL INTERLUDE
For your listening enjoyment, and general encouragement, we continue Wheatie’s tradition of fine music videos, shipped fresh from the seas of information by our intrepid authors.
First, some “epic” mandolin…..
Well, let’s get that mandoleen a little more TOE-TAPPIN’ and a FOOT STOMPIN’!
And finally, a song from a movie you probably never saw – Captain Corelli’s Mandolin.
OK – we can’t leave you with that downer. Check THIS happy song out!
Feel ready? GOOD!
Call To Battle
Our beloved country is under Occupation by hostile forces.
Daily outrage and epic phuckery abound.
For the first time – no image here.
OK, just ONE of many:
I refer you to a series of ABSOLUTELY AWESOME memes posted by Robert Malone, here:
“Hospitals receive payments for testing every patient for COVID, every COVID diagnosis and every ‘COVID death,’ as well as any time they use remdesivir and mechanical ventilation.”
Not only is that a great article, that is highly referenced.. It very accurately goes through history and malfeasance by our government and the hospitals. This article is a must read. It also has an extensive list of references at the end.
You may hit a paywall, but you can take Malone’s word for it, if you do.
H/T whoever it was who found this gem! (I forgot)
How “Let’s Go Brandon” Demonstrates the Failure of The Regime’s “Decisive Victory” Strategy Against Us
This may seem like it’s the usual, hand-waving, “defeat is victory” battered-conservative abuse-porn, coated with addictive hopium, but IMO it’s actually some “real” hopanite ore, suitable for creating hopium-based nukes, and depleted hopium bullets.
Basically, a comparison of the “establishment victory over Trump” to Pearl Harbor.
They have not won.
Rather, they have earned themselves an ASS-WHOOPIN’.
Robert Malone Performs/Explains A Real Live Peer Review
This is actually REALLY GREAT, and a UNIQUE OPPORTUNITY. You will almost NEVER see this, unless you get an advanced science degree, and in that case, you will likely be taught all the bad habits of somebody not nearly as good and experienced in “grantsmanship”, patenting, and publication, as is Robert W. Malone.
Malone even does it in plain, common, sensible language that anybody can understand. You will literally see how to “talk back” to HIGHLY credentialed scientists making mistakes, showing bias, sticking to narratives, and just being people who you should NOT trust.
This is RESTORATIVE to real science. I just cannot praise this enough.
Peer review example: “Effectiveness of the BNT162b2 vaccine among children”
Having written hundreds of requested peer reviews, I am offering my unsolicited one.
What makes this even more powerful, is a slightly earlier post by Malone, in which he exhorts ALL people to USE COMMON SENSE in doubting the media on things in which they don’t have expertise, because the FAKE NEWS is demonstrably WRONG on the things in which you DO have expertise, and you REMEMBER those cases, and therefore you are absolutely entitled to extend that skepticism to ALL THINGS THE PRESS SAYS.
Please note that there are many variations on how English speakers actually pronounce most of the word, but the lifted pinky / beltway bandit / light-in-the-loafers silent T is “supposed to be” preserved in English, and the result sounds very French.
Therefore, if you want to stay grounded and keep your “man of the people” cover, you can intentionally mispronounce the word JUST A LITTLE by including that final ‘t’ ever so slightly (“MAUWNt”).
Alternatively, over-emphasize the open mouth ‘MAUW[n]’ at the end to almost comedic levels, and you sound like a real American who took French in high school. But it’s still probably best to avoid ‘reproach-ment’, unless you really want to make sure people think you don’t know a lick of French.
Used in a sentence:
The convergence was noted by statesmen and scholars of the time, but the term “Great Rapprochement” to refer to a distinct historical phenomenon may have been coined by the American historian of Anglo-American relations Bradford Perkins in his 1968 study of the period, The Great Rapprochement: England and the United States 1895–1914.
Slightly misused (and optionally mispronounced) in a Lindsey Graham joke:
And we’re finally serving a NORMAL DRINK tonight. Even though it’s a SECOND ROUND.
STAY TUNED…..
While our beloved REAL bartender takes a needed break of unknown duration, we continue to ENDEAVOR TO PERSEVERE.
and what time of year is it now???
Christmas Spirit
We continue our WAAAAAY too-long celebration of Christmas by noting that some of our neighbors STILL have their lights and decorations up.
We saw a nice red Christmas bow laying in somebody’s yard by their driveway.
We ourselves just got rid of our tree.
And TODAY is the 25th of the month. That’s VERY “Christmassy”.
So yeah. Given that there are a few daysweeks months AFTER Christmas where it’s STILL Christmas, that means we have a few more weeks left. Riiiiiiight?
Sure! So have some hot CHRISTMAS chocolate!
And now, the rules of the pub.
HOUSE RULES
God bless us, every one! Tiny Tim had such a beautiful soul. He hadn’t a mean bone in his body…unlike most of us. But in keeping with Christmas, we promise to honor Wolf’s rules and keep Scrooge at bay. The Utree is where the Ghost of Christmas Present will conduct you should you need to rattle some chains. Another option, should all hell break loose is here.
Now, back to business.
AMEN!
Free the January Brothers!
Current Art On The Wall
We’re just gonna segue into the next item with our selection, if that’s OK.
This gets a bit “planetary”…..
Venus and Mercury Instructing CupidChristiaan Huygens, Saturn, and SomethingRaindrops on Titan
…..which was based off of an FDA alert (sketchy link)…..
…..which actually links back to a different CDC alert (even sketchier link)…..
WHATEVER.
Here is that final CDC alert. Only the top 3 paragraphs are important here.
Let me quote the text of those first 3 paragraphs for Zoe. I will make BOLD what is important.
Dear Partners in Prevention,
December 20, 2021
I’m writing to share the U.S. Food and Drug Administration (FDA) alert sent to clinical laboratory staff and health care providers about a syphilis test. The alert reports that false reactivity, or “false-positive,” Rapid Plasma Reagin (RPR; non-treponemal) test results, when using the Bio-Rad Laboratories BioPlex 2200 Syphilis Total & RPR kit, can occur in some people who received a COVID-19 vaccine and includes recommendations for addressing these potential false positives.
Historically, false-reactive RPR test results have been observed in people with systemic infections unrelated to syphilis, such as tuberculosis, rickettsial diseases, and endocarditis.False-reactive RPR testing also has been previously observed following immunization (specifically following smallpox vaccine). False reactivity with RPR can also occur during pregnancy.
Per CDC’s 2021 STI Treatment Guidelines, reactive RPR results should always be confirmed with treponemal testing (e.g., Treponema pallidum particle agglutination, TP-PA). This is, in part, because of the above-mentioned issue: false-positive nontreponemal test results can be associated with multiple medical conditions and factors unrelated to syphilis. According to FDA’s alert, treponemal testing for syphilis does not appear to be impacted by this issue.
Allow me to translate.
It turns out that “being vaccinated for COVID-19” throws off an ANTIBODY-BASED SYPHILIS TEST, and can give false positives.
The reason is that these are a sort of antibodies against substances released from cells attacked by certain diseases and conditions. Thus, they’re not exclusively the downstream product of syphilis.
Normally, certain diseases, certain vaccines, and pregnancy can all throw off this more rapid but less conclusive syphilis test, and that is part of the reason why people are supposed to follow up this easier test, with a test that looks for the actual organism which causes syphilis.
Thus, we have added one more cause for the test to be thrown off.
This is not the same as the HIV test that was thrown off by a particular Australian vaccine, because the antigen in the vaccine actually contained an HIV protein (gp41) as part of the vaccine, and created antibodies against HIV. I talked about that last week. That was a much more direct test interference, easily expected.
How a Psycho Vaccine Marrying the Infamous COVID Spike Protein to HIV’s Neurotoxic gp41 Was [Allegedly] Canned by a Mere Testing SNAFU How Australia Dodged The First Mad Vax Bullet of the WEF Scamdemic / Plannedemic Darwin Award Vaccine Featured Insane Merger of HIV and COVID But Failed Due to Buggering of AIDS Tests, NOT …
What I find interesting is that one of the things that normally sets off the syphilis test is endocarditis.
Endocarditis, which is inflammation of the inner surfaces of the heart, is one of the three main heart inflammations, thus being pretty damned close to myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the outer sac), both of which have very prominent correlations to the jabs.
So while this means that – NO – the shots are not giving people syphilis – the shots ARE basically acting like an illness, and very much like a known cardiac illness.
You were warned.
Now – while I was researching syphilis, I became interested in the treatment with compounds of mercury.
Traditional mercury-based pastes were used in cures. Whilst this was partially effective, the toxic side effects of the mercury probably outweighed any advantages.
This is actually a HUGE understatement.
It turned out that arsenic was considerably better.
It wasn’t too long after that success, that penicillin took over as the real cure for syphilis.
I will come back to MERCURY in a future post, because I found something quite amazing in its history.
But if you look ONE COLUMN TO THE LEFT and TWO ROWS UP…..
COPPER is also bacteriostatic and algicidal – and at concentrations below where it is a health risk. And THAT leads back to a DRINK that Grandmaintexas introduced us to……
Moscow Mule Revisited
Based upon my reading of Grandma’s post on the subject, the Moscow Mule simply is not a proper Moscow Mule unless it is served in copper vessels.
The health effects of COPPER are about as debatable as the effects of mercury – although, in general, copper is much less toxic, so when it’s being “not good for you”, it’s a lot less “not good for you” than lead. At the same time, copper is much MORE toxic to things like algae, fungi, plant roots, and other “pests”, than it is to us, and that is why it is found among the gardening pesticides in hardware stores. The antimicrobial activity of copper is extremely well-documented, but appears to be complex. Simply having copper in the household or workplace environment seems to have health benefits – and this was particularly noted back in the days of less sanitary environments. Water passing through copper fixtures tended not to spread disease.
We tend to forget about OLD SCIENCE, so we can’t put new things into good perspective.
LEAD and other CHEMICAL ADVANCES saved us from the horrible BIOLOGICAL diseases and maladies of the uncivilized life.
Did they have chemical consequences? Yes. The TRICK is REMEMBERING AND ADMITTING OLD RISKS AND BENEFITS while also DISCOVERING AND ADMITTING NEW RISKS AND BENEFITS, then BALANCING HONESTLY with the PROPER PRIORITIES which put PEOPLE FIRST.
It is VERY easy to see where CDC went off the rails with the COVID-19 vaccines, being unable to admit old benefits (of lasting immunity to caught and treated diseases), while also being unable to admit new risks (of vaccines using untested and immature technologies).
Likewise, looking back, it is easy to see that basic sanitation – not vaccination – REALLY conquered diseases. Vaccines came in, mopped up, and took all the credit, by design, because bad people realized that vaccines in the hands of a technological elite, combined with an ignorant populace they can essentially murder and experiment on at will, allow them to basically FARM HUMANITY.
Sorry, Bill Gates. We understand your social engineering of us. We know your M.O. We know your real intentions. Including for the “people of color” you pretend to care about.
You will note that, in general, the further down the periodic table one goes, the more toxic the metals. Surprisingly, the second-lightest one – beryllium – is quite toxic, but even lightweight aluminum simply isn’t all that bad, in the big picture (but you’ve got to keep it on the OUTSIDE). In contrast, if you get down and heavy there with mercury, thallium and lead, or even as far down the table as cadmium and indium, the metals can be quite toxic.
Lead used to be used for plumbing – enough to lend its name to the profession. Copper then took over – before plastic began to displace copper. Nevertheless, copper is still highly valued for plumbing, as well as for electrical wiring.
As noted above, copper in drinking water is an interesting beast. Lead and copper in drinking water are controlled by the EPA under something called the Lead and Copper Rule, or LCR. Note that the linked document, which talks about the most recent “upgrade” to the rule, is over 400 pages. Yeah – there is a MESS of goofiness outside the actual rule there. Most of the concern is about lead, which is now highly restricted. Here is all that is said about copper’s toxicity in the linked explainer:
Acute copper exposure causes gastrointestinal distress. Chronic exposure to copper is particularly a concern for people with Wilson’s disease because they are prone to copper accumulation in body tissue, which can lead to liver damage, neurological, and/or psychiatric symptoms. For a more detailed explanation of the health effects associated with copper see Appendix E of the final rule Economic Analysis (USEPA, 2020). EPA did not propose revisions to the copper requirements; thus, the final rule does not revise the copper requirements.
Copper is basically off the hook at 1.3 ppm or below. That number has not been upgraded. Why is that level important? In my opinion, it’s because copper is bacteriostatic and algicidal in practice at between 0.1 and 1.0 ppm. Thus, one can SAFELY DRINK water which is being purified against microorganisms with copper.
And THAT would include the Moscow Mule, depending upon how long it sits.
I refer you now to an excellent article, which relies on a breathless scaremongering headline, but actually DOES provide a balanced set of viewpoints on both the DANGERS and BENEFITS of dietary copper.
Sipping This Popular Cocktail Is a “Health Hazard,” Experts Say
AFTER 27 MINUTES, YOU MAY BE AT RISK OF HEAVY METAL POISONING.
First of all, copper isn’t really a “heavy metal” IMO, but whatever. It’s heavier than some.
You will note, after reading at the link, that you have to drink a ton of Moscow Mules, or a few that have sat around for a very long time, to MAYBE get sickened by them.
In general, avoid drinking acidic things that have been in contact with copper for a long time, and you will be OK.
Remember – most household water has sat around in copper pipes for quite a while at neutral pH, and it’s simply not toxic (due to copper). You DO get less lead if you flush your water 30 seconds before getting drinking water, but again – we’re talking about levels that would make Romans, Victorians, and even people from 70 years ago howl with laughter at our prissy over-concern – even knowing the science.
Perspective is very important – as you are about to see in a beautiful example of the failure of modern science, thanks to CCP socialism infecting both global science and science publishing.
Failure of Socialized Science and Peer Review Exposed in a JAMA-Published Ivermectin Study
The fact that Pierre Kory now calls JAMA “PHAMA” is a nice short way of saying that medicine has been utterly taken over by the pharmaceutical industry, and IMO set back several thousand years. Hippocrates would be HORRIFIED by what has happened to medicine – and I say that as somebody OUTSIDE medicine, and a lot closer to the pharmaceutical industry.
IMO it’s too late to save the pharmaceutical industry from scandalous criminal survival – but it’s not too late to save the profession of medicine from utter moral death. And thus, you will be treated to my following scientific opinion.
Steve Kirsch doesn’t play defense. He saw how JAMA (the Journal of the American Medical Association) completely FUMBLED an ivermectin paper, and how Pierre Kory picked it up off the ground, taking complete control, but more or less just standing there, lamenting the bad refs and horrible cheating. So Kirsch did the only thing he does. He grabbed the ball from Kory and ran it back for a touchdown.
“New JAMA paper show Ivermectin blows the COVID vaccines out of the water”
This is an utter reversal of the conclusion of the paper.
All because some guy in the stands named “Massimaux” spotted the free ball and yelled “FUMBLE!!!”
If you understand science, and science publishing, then you will see that what Kirsch did here was BRUTAL. And I’m gonna show you where all the bruises and black eyes are.
I almost feel sorry for JAMA, but not enough to miss this opportunity to LEAP ONTO THE DOGPILE and give AMA’s hare-brained PC leadership a good WEDGIE.
Don’t worry about the AMA. They’re protected by Pfizer, Biden, and the media. And just like any good mafia arrangement, as long as AMA keeps saying the right things, and not saying the wrong things, everything is gonna be OK.
Everything but science. But that’s OK, too.
We’ll take care of things. Just like we did here.
Here is the Kirsch gab that grabbed my attention.
Repeating for Zoe, as well as our silicon friends…..
“Wait a second. I thought there was some paper just out that Alex Berenson said was basically the end of ivermectin, although scientifically, I know that’s pretty much impossible. I know there is SOME explanation for why this paper (which I have not read yet) has to be deviating in some way from the MANY papers that show limited but solid efficacy – and especially against DEATH – just like HCQ. But this CANNOT be the same paper. No way! Kirsch would not be saying this unless the results were stunningly IN FAVOR of ivermectin, and there is no WAY that some authors with a NEGATIVE-LEANING study would be……. I mean….. WHAT THE HELL????”
SO – I just stopped to see what in the hell paper Kirsch was talking about.
Now we’ve discussed (in the comments on this site) Berenson’s very weird attack on Robert Malone when they appeared together on Fox News, which didn’t make sense THEN, but which does NOW – and I will explain that momentarily. But first, back to Kirsch.
Kirsch explains that – YES – this paper states in BOTH its abstract and its conclusion the following:
“The study findings do not support the use of ivermectin for patients with COVID-19.”
However, that is NOT what the data says.
Certainly not to everybody.
Certainly not to me.
In other words, DIFFERENT scientists (like Kirsch, Kory, me, and an anonymous Twitter poster names Massimaux, who found the key issue) have looked at the data, and see something quite different.
Kory goes into a rather long analysis of the whole war against ivermectin, but Kirsch digs into Kory’s article and then finds and elucidates the key nugget – discovered by Massimaux – that just ends the arguments.
It helps to read this in Kirsch’s article, but if you’re going to be lazy, I’ll explain here.
Here is Massimaux’s tweet:
In the I-TECH study, of 490 patients, 241 got Ivermectin and 331 were vaccinated.
Can we compute the vaccine effectiveness AGAINST DEATH and Ivermectin effectiveness AGAINST DEATH? Yes, we can! See the figure.
Look at the bottom line in the two tables and compare. Not only is ivermectin CLEARLY better than the vaccine at preventing death – the significance of the result is significantly greater.
If the efficacy of ivermectin against death is not true, then very little else in the study is true.
This data says that ivermectin is exactly what we’ve been saying it is. It’s not a miracle cure, but it WORKS – particularly in preventing DEATH – its only real purpose. That result is IN THE PAPER. It is IN THE DATA. And if the authors want to argue that it’s not in the data, because it’s not significant enough, then nothing ELSE is in the data, because most everything else is even LESS significant.
Now it’s very important to realize that this nice little pair of tables FROM THE DATA is not due to the original authors – it’s due to a POST-PUBLICATION “peer review” by somebody who looked at the very same data, and PROVED using the authors’ own data that they were WRONG to say that the data didn’t support use of ivermectin.
So why did the authors tack on that wrong statement?
Did the EDITORS make them tack on that statement? Did the AUTHORS tack it on to get the paper to publish? Or is the “peer bias” against ivermectin, mostly due to the media, SO STRONG that scientists didn’t even look through their own data to see a conclusion they didn’t want to see?
Or is it a combination of ALL of these?
It is clearly in the data that ivermectin is three times as effective as the vaccines in preventing death. Even more importantly, if you add in what is known OUTSIDE the paper in question – namely the adverse effects of the vaccine and the safety of ivermectin, then it’s a no-brainer to NOT take the vaccine and to just use ivermectin. And Kirsch explains THAT rather nicely.
The data LITERALLY justify our position.
This was my hunch all along, and as vaccine side effects loomed larger and larger, and ivermectin proved to be rather shockingly harmless, even at antiviral doses comparable to large-animal systemic antiparasitic doses. All ivermectin had to do was prevent death to some moderate extent, and it was a no-brainer that people should take it.
To conclude anything else, based on the data, is murderous folly, in my opinion.
When I was a young lad – a mere student – but also one who WROTE PAPERS (because I had a great professor who TRAINED US to be full-blooded scientists), we EXPECTED to be CRITICIZED in peer review by people exactly like Steve Kirsch, Pierre Kory, and myself. We expected that others would look at data and see it completely differently.
And we would then have to ACKNOWLEDGE the alternative interpretations, or convince the editors that the criticism was not even worth acknowledging (a VERY rare occurrence in any legitimately contested field).
My lab had PRACTICE criticizing other people’s work – and we expected it in return. I personally found quite a few errors in the literature. Most were small – mostly problems of the writing – but some were huge and affected the science. Sometimes the big errors would only partially alter the author’s conclusions, but other times they had a significant impact.
However, I have to admit that I never ran into data which PROVED THE OPPOSITE of the authors’ main conclusion – even if only to the critic – and THAT is what we have here.
PEER REVIEW is designed to subject a paper to (hopefully at least TWO) critical readers who will very likely DEMAND improvements. Those improvements often mean acknowledging DIFFERENT views of the data as being possible and maybe even reasonable.
That kind of QUALITY peer review was VERY OBVIOUSLY not done here.
What we have RIGHT HERE is a demonstration that HERD REVIEW is much more important than PEER REVIEW.
PEER REVIEW is subject to BIAS. It is subject to SUBVERSION and GAMING.
I go back to the Zhang mask paper, for crying out loud.
To me, this will always remain a horrifying example of “fitting the data to the theory”, rather than looking to see what the data says. You can just look at this graph and see the crime.
I lay this stuff SQUARELY at the feet of SOCIALISM, which has politicized science and removed control of science from the people of science themselves, investing much of it in a media which WILL NOT question government narratives. People raised under socialism who become “go-alongers” – and so SOME degree that is everybody – stop questioning things that need to be questioned.
I have WATCHED and I have SEEN how WEF and CCP corruption have degraded science everywhere.
They’re not going to fix this stuff – at least not yet.
But until then, know this:
Ivermectin WORKS, and it was just proven by people who said it doesn’t work.
Thanks to HERD REVIEW.
One last point.
Why did Alex Berenson not see this?
IMO, it’s because Berenson is simply not a scientist – he’s an investigative journalist. Thus, his virtue-signaling attack on Malone was meant to show “journalistic balance”, NOT that he himself had deeply researched the history of the topic, in which case he (Berenson) would have likely said “Yes, Malone really is the most foundational of the founding fathers of the tech.”
But let’s not blame Alex too hard. THE AUTHORS OF THIS STUDY – that’s right – the authors themselves – didn’t see it, either.
See what I’ve always said? Real science is contentious.
But it has a good heart.
It wants the TRUTH.
ENJOY THE SHOW.
Thank you all for being here. Have a great weekend.
How a Psycho Vaccine Marrying the Infamous COVID Spike Protein to HIV’s Neurotoxic gp41 Was [Allegedly] Canned by a Mere Testing SNAFU
How Australia Dodged The First Mad Vax Bullet of the WEF Scamdemic / Plannedemic
Darwin Award Vaccine Featured Insane Merger of HIV and COVID But Failed Due to Buggering of AIDS Tests, NOT Because of the Obvious Risks
Was It Ever Really For COVID? The gp41 HIV Protein is a TOP Target For AIDS Vaccines
How Science Monetization and Corruption Has Broken All Vaccine Safety Mechanisms and Made Sneaky Liars Out of Scientists
Mood Music
Intro – Prepare To Be Shocked
This is one of the craziest stories your either never heard, or barely heard. I am certain of the following. Nobody ever spelled out to you how NUTS this failed vaccine really was. This absolutely bonkers vaccine, that was almost used on all Australians.
The fact that nobody even followed this story, shows that the captured corporate media is absolutely not doing its job. Either THAT, or their job is to help deceive us.
And you know where my money is on that.
Surely, in the past, both journalists and scientists might have said something to the effect of “Hey – marrying a cardiovascular pathogenic bat virus spike protein and a neurotoxic AIDS protein in a vaccine to prevent a cold seems a little weird.”
BUT NO. NOT NOW.
And yet, some of us, few as we might be, might still have some questions.
We assume – ASSUME – as in ASS / U / ME – that all people in all of science are acting in all of our best interests all the time.
I have been completely broken of this spell, and I can tell you – what I can see now is not pretty.
I need to prepare you for what I’m about to tell you.
State of Corruption of Vaccine Science
First, a fantastic interview of Dr. Robert Malone by Tucker Carlson. It’s very folksy and long – a bit over an hour – but it will absolutely cure you of any idea that science in 2022 has not been almost totally corrupted by money, power, and SECRET AGENDAS.
This guy Malone is as close to a Moderna insider / honest outsider as you’re gonna get, and he clearly sees the dirty play from the Moderna point of view.
Hat tips to FG&C and GA/FL for keeping this video in play. Gail has been pumping this video, too. EVERYBODY need to watch this.
Indeed, let’s just save that tweet as an image, in case Twitter decides Jack is becoming too much of a liability.
One of the biggest BOOMS dropped in the video, IMO, is the fact that Robert Malone WARNED the FDA about the toxicity of the spike protein, and they SHRUGGED IT OFF.
Yes. Malone gave them documentation, as asked, and they came back to him and said everything was OK. And THAT is when he started to think something was very wrong.
We’re about to do it AGAIN – only I’m not the first – I’m just rediscovering an obvious “why the heck are they doing THAT” point.
But we’ll get to that in a minute. We need to broaden our list of corrupt suspects.
You see, corporate “science” isn’t the only bad actor here. What about governments that conspire with the corporations to “mandate” their products for a mutual PAYOFF?
It turns out that both Justin Trudeau and the Canadian government have a very large incentive in mandating the broken, dubious, and just plain BAD Moderna and Pfizer “vaccines”.
When you realize that Justin Trudeau is not only following his mandate madness for WEFfian ideological reasons, and for Papa Fidel power, but also for CASTRO CASH, you understand what’s REALLY going on.
SO – now that you realize THESE PEOPLE care more about other things, than they care about us, the following will make more sense.
The Frankenvax That Almost Was
So just today, FG&C posted THIS TWEET which made me go WTF…..
Basically, an Australian COVID vaccine that falsely triggers AIDS / HIV tests was recalled. The vaccine was NOT sent out for use by the public, because it gave people positive AIDS tests.
GREAT, but…..
WHY did the vaccine do this? And by the way….
Didn’t this happen BEFORE – like over a year ago?
I could have SWORN this happened before.
Is this OLD NEWS or a DIFFERENT VACCINE?
Or did they bring the SAME vaccine BACK?
Or even worse….. AND logic…..
You see, I remember something just like this bit of news, over a year ago. It was some vaccine from an Australian university that accidentally triggered AIDS tests.
Well, when I looked closer at this, it turned out to be THE SAME NEWS. Meaning that this recent tweet was just OLD NEWS.
HOWEVER – I happen to know a lot more now, a year later, so I dug DEEPER and FOUND MORE.
And now I want to explain to you, exactly what is going on.
Because this monster AIN’T DEAD.
VolksWackcine 451
Let’s begin by looking at the actual announcement that all this news came from. The paragraph in BOLD is the critical one. If you’re going to TL;DR past all the rest, read THAT paragraph.
Friday, 11th December, 2020: The University of Queensland (UQ) and CSL today announce that the Phase 1 trial of the UQ-CSL v451 COVID-19 vaccine has shown that it elicits a robust response towards the virus and has a strong safety profile. There were no serious adverse events or safety concerns reported in the 216 trial participants. However, following consultation with the Australian Government, CSL will not progress the vaccine candidate to Phase 2/3 clinical trials.
The University of Queensland commenced a Phase 1 trial of their COVID-19 vaccine candidate – v451 – in July 2020, to assess safety and immunogenicity in healthy volunteers. CSL was working towards taking responsibility for the Phase 2/3 clinical trial and large-scale manufacture of the vaccine, upon completion of successful trials.
The Phase 1 data also showed the generation of antibodies directed towards fragments of a protein (gp41), which is a component used to stabilise the vaccine. Trial participants were fully informed of the possibility of a partial immune response to this component, but it was unexpected that the levels induced would interfere with certain HIV tests.
There is no possibility the vaccine causes infection, and routine follow up tests confirmed there is no HIV virus present.
With advice from experts, CSL and UQ have worked through the implications that this issue presents to rolling out the vaccine into broad populations. It is generally agreed that significant changes would need to be made to well-established HIV testing procedures in the healthcare setting to accommodate rollout of this vaccine. Therefore, CSL and the Australian Government have agreed vaccine development will not proceed to Phase 2/3 trials.
The Phase 1 trial will continue, where further analysis of the data will show how long the antibodies persist, with studies so far showing that levels are already falling. The University of Queensland plans to submit the full data for peer review publication.
UQ Vice-Chancellor, Professor Deborah Terry, said while the outcome was disappointing, she was immensely proud of the UQ team who had shouldered a heavy burden of responsibility while the world watched on. “I also want to thank our many partners, our donors – including the Federal and Queensland Government – and of course the 216 Queenslanders who so willingly volunteered for the Phase 1 trials.”
UQ vaccine co-lead, Professor Paul Young, said that although it was possible to re-engineer the vaccine, the team did not have the luxury of time needed. “Doing so would set back development by another 12 or so months, and while this is a tough decision to take, the urgent need for a vaccine has to be everyone’s priority.”
“I said at the start of vaccine development that there were no guarantees, but what is really encouraging is that the core technology approach we used has passed the major clinical test. It is a safe and well-tolerated vaccine, producing the strong virus-neutralising effect that we were hoping to see.
So we will continue to push forward and we are confident that with further work the Molecular Clamp technology will be a robust platform for future vaccine development here in Australia and to meet future biosecurity needs.
Dr Andrew Nash, Chief Scientific Officer for CSL said “This outcome highlights the risk of failure associated with early vaccine development, and the rigorous assessment involved in making decisions as to what discoveries advance.”
“This project has only been made possible by the innovative science developed by world-class scientists at The University of Queensland and the strong collaboration between our organisations, and many others, over the last 10 months. CSL and Seqirus are committed to continuing our work to protect the Australian population against COVID-19. Manufacture of approximately 30 million doses of the Oxford/AstraZeneca vaccine candidate is underway, with first doses planned for release to Australia early next year. In addition, CSL has agreed at the request of the Australian Government to manufacture an additional 20 million doses.”
UQ and CSL acknowledge the support of the Coalition for Epidemic Preparedness Innovations (CEPI) in partnering to enable the rapid development of the vaccine candidate through clinical trials.
So what they’re saying is that this vaccine – which uses the HIV protein gp41 – sets off HIV tests. And THAT made the test unacceptable to move forward. The remaining phase II and phase III trials were cancelled, while the phase I trials continued to finish collecting data.
And WHILE they say that the phase I testing showed that the vaccine was safe and effective, if you look more closely, they only tested it on 216 people.
We KNOW from the Moderna and Pfizer tests, that even after HUGE phase II and phase III trials, using thousands or tens of thousands of participants, there are serious side effects that are STILL not discovered until actual roll-out to the public, when millions receive the shot.
And that does NOT include long-term effects. We know NOW that this determination can be critical in many cases.
And one more point for the record. As you can see by the statement at the end of the press release, this vaccine was supported by the Bill Gates organization CEPI.
Yeah, that CEPI, and THAT Bill Gates.
Like I say, CEPI is how Gates gets TWO VOTES, and GAVI is how he gets THREE.
So the bottom line – this vaccine was killed because it set off AIDS tests.
But let’s dig a little deeper into that.
So What’s With HIV and the COVID Vaccines?
When I first heard about this particular Australian vaccine (UQ-CSL v451, or v451 hereafter) triggering HIV tests, my immediate thought was that this might be proof that the Indian researchers were CORRECT – that the spike protein really contained those four inserts from HIV, and that THIS was setting off tests for HIV.
Later, I heard that – no – there was actually some segment of HIV protein being used in the v451 vaccine INTENTIONALLY. Thus, the whole problem seemed stupid, the use of the HIV protein seemed short-sighted, and I promptly forgot about it. No smoking gun – just a stink bomb.
However, a year’s time changed all that.
Think how different the perspective is now.
virus almost certainly came out of a biowarfare lab in China with PLA/NIH ties
Fauci, Dazsak and minions now known to have LIED about origins
Fauci gang also lied when pooh-poohing the Indian HIV insert hypothesis
mRNA vaccines seem to be producing immune deficiency, a.k.a. “VAIDS”
there are working hypotheses now which explain immune deficiency
Fauci’s history with HIV mirrors current history with COVID – lies and hidden agenda
Fauci seems to be obsessed with immunodeficiency and vaccines
Fauci promoted bad killer drugs as treatments in both cases (AZT, remdesivir)
Fauci seems to have an agenda clearly counter to truth as we know it, and is likely serving something beyond the increasing “fake” science which the public believes is operant in the world, but which is very likely a “reduced set” intended to deceive us
Thus, with all that WEIRD background, it NOW seems a bit “par for the course” that somebody in that world would want to bring HIV into the COVID equation.
But is that a good idea?
Now – before I go talking about why this might be a BAD idea, I want to give you plenty of references as to why they SAY it was a good idea.
Let’s start with a good explanation of why the false positives occurred. This article includes a lot of information on the v451 vaccine itself.
The article mentions, without too much detail, that the HIV protein is part of a “molecular clamp” – a trimeric molecular “holder” of spike protein molecules. This holder allows three molecules of any attached spike-type protein to stay locked into a rigid, parallel conformation, which will remain in the desirable pre-fusion (with a cell) configuration, and not change into the useless post-fusion configuration.
The article also links to a scientific paper on the technology:
Prior to 2020, the threat of a novel viral pandemic was omnipresent but largely ignored. Just 12 months prior to the Coronavirus disease 2019 (COVID-19) pandemic our team received funding from the Coalition for Epidemic Preparedness Innovations (CEPI) to establish and validate a rapid response pipeline for subunit vaccine development based on our proprietary Molecular Clamp platform. Throughout the course of 2019 we conducted two mock tests of our system for rapid antigen production against two potential, emerging viral pathogens, Achimota paramyxovirus and Wenzhou mammarenavirus. For each virus we expressed a small panel of recombinant variants of the membrane fusion protein and screened for expression level, product homogeneity, and the presence of the expected trimeric pre-fusion conformation. Lessons learned from this exercise paved the way for our response to COVID-19, for which our candidate antigen is currently in phase I clinical trial.
Here is part of a really good graphic from the paper.
You can see how it’s possible to produce a spike protein with the “molecular clamp” attached, and then simply let this recombinant construction TRIMERIZE (form a triple, side to side) around the three molecular clamps, and thereby stabilize the three spike protein molecules next to each other.
This is a bit like a “motif” within an actual virus, where spike proteins, sticking out next to each other, protect each other’s sides. THAT is the basic idea of this thing.
Remember how Novavax assembles a bunch of spikes via modified ass ends into a kind of antigenic cloved apple, to create a kind of fake virus? Same very basic principle.
Indeed, the molecular clamp is even a bit like TWO motifs, since gp41 serves a somewhat similar purpose in the HIV virus, being the root of a stalk to an attack mechanism.
HIV-1 fusion process. It involves both subunits of the envelope spike complex. Notably, gp41 is shown in green with its transmembrane region buried in the virion membrane, both segments of heptad repeats (CHR closer to the virus and NHR closer to the host cell) before and after conformational changes, and the N-terminal end of the ectodomain in gray. In the last two panels pointed out by the red arrows, gp41 is observed following penetration of the host cell and following a conformational change resulting in the six-helix bundle which brings the viral and cell membranes into close proximity.
So – in a very real sense – this whole “vaccine” thingie is a literal marriage of HIV and coronavirus – the simplest possible one.
And they didn’t tell you ANY of this shit – did they?
So all of that WORKS, but the problem is that antibodies don’t just form to the attached spike protein – they ALSO form to the “molecular clamp”, meaning to the gp41 protein.
And what does that mean?
An AIDS Vaccine in Disguise?
The people who made the v451 vaccine say they didn’t expect there to be so much antibody response to the gp41 parts of the vaccine, thus triggering HIV tests.
You know what?
I don’t believe them.
I think they were gaslighting us all along.
Part of this is due to the fact that I’ve seen gp41 named numerous times as a potential basis for subunit vaccines against HIV. In fact, in one reference, I saw it named as THE BEST HOPE for an AIDS vaccine.
They didn’t mention that? LOL. OH, REALLY.
So WHY would anybody be using gp41 as part of an antigen, and not expect it to generate antibodies?
In fact, one might almost look at this v451 vaccine and regard it as an HIV vaccine, with spike proteins tacked onto gp41 as a kind of “nasty adjuvant” to initiate the immune response to the HIV protein.
Seriously – which is the real target here – COVID or HIV? Or BOTH?
This looks to me like a perfect example of…..
WAIT FOR IT….
“REVERSO”.
But let’s just set that aside for now, and pretend that the thing which COULD be a vaccine for EITHER ONE of the two things they stuck in it, is REALLY a vaccine for the fakey-fake cold that we don’t need a vaccine for, and NOT a vaccine for the sexual disease that stands in the way of Luciferian scum creating their polyamorous sexual paradise of literal epic random phuckery.
OMG, these people have just lied, and lied, and lied again. And they will KEEP lying.
But we’ll pretend they’re not lying, for just a little while longer.
So if we have an actual COVID vaccine here…..
…..is it a good idea to include the HIV gp41 protein subunit?
Well, after what we’ve seen with the spike protein, I was thinking maybe it wouldn’t be.
And it turns out, I wasn’t the first person who thought of this.
Doorless Carp’s Suspicious Cat In A Box
When I went looking for the toxicity of the gp41 protein, one of the first things that came up was some guy or gal who appears to have been actively suppressed on Twitter, eventually banned to Gab, and whose substack article on the topic has only two likes – ONE OF THEM MINE.
Doesn’t mean the article’s not important. And I think it’s about to get a few more hits.
This is a wonderful article that is simply SKEPTICAL of the entire “it was pulled because of triggering AIDS tests” reasoning.
DoorlessCarp read the same press release I cited above, and pokes and prods it from the point of view of somebody who knows a heck of a lot about HIV and AIDS, and doesn’t buy what (s)he’s reading in that press release. Something doesn’t sniff right to “them”, and “they” spell out the issues.
I will attempt to summarize DoorlessCarp’s concerns (noted as “DLC” hereafter).
First, DLC admits to actually being led to the problem by one of those Fake News “straw man fact checks”, which attempt to either “debunk” facts or mislead scandals by setting up an adjacent strawman and knocking it down. OBSERVE.
“Fact check: An Australian vaccine trial did not give trial participants HIV”
LOL. No. The truth they’re protecting is that the “COVID vaccine” gave them HIV antibodies, and it was very likely the whole point.
To quote DLC about the Aussie vaccine researchers: “I wouldn’t let these clowns dispense aspirin, let alone design fast tracked vaccines.“
DLC then makes this statement, noting that there is a curious skew between the reality of HIV testing and the idea that there is some kind of a problem here.
Interesting rapid response to the effect that antibody only HIV tests have long since been debunked as a diagnostic tool on their own due to cross reactivity from other antibodies. They don’t tell you anything useful.
DLC then quotes extensively from this letter which explains why HIV testing via antibodies is actually a rather horrible mishmash of false positives and negatives, ultimately requiring a clinical diagnosis and “validation by lifestyle facts”.
Which leads to the next section, which I quote:
So what was the real reason for pulling the Australian trial, was it the gp41 toxicity?
The antibody problem raises more questions than it answers as spike S2 has homology to P24, GP41 and GP120.
This is dark stuff, P24 has been ported straight across from HIVs capsid to the spike protein. Here’s the proof, at least as far as what specific antibodies are telling us, which don’t lie:
What is p24 antigen?
“One distinctive HIV antigen is a viral protein called p24, a structural protein that makes up most of the HIV viral core, or ‘capsid’. High levels of p24 are present in the blood serum of newly infected individuals during the short period between infection and seroconversion, making p24 antigen assays useful in diagnosing primary HIV infection.”
suspects the real reason for pulling the vaccine was the toxicity of gp41
notes that the spike protein already has potentially dangerous homologies to three HIV proteins, p24, gp41 and gp120
p24 is basically the nucleocapsid protein of HIV
p24 tends to be detected early in the AIDS process, before antibodies to it form
DLC then cites several papers demonstrating that there is already a lot of understanding of antibody cross-talk between the SARS-CoV-2 spike protein and either (1) original SARS-CoV proteins, and (2) HIV-1 proteins.
In the latter case, there is specific interaction with gp41.
References given:
The SARS CoV-2 spike directed non-neutralizing polyclonal antibodies cross-react with Human immunodeficiency virus (HIV-1) gp41 (Dec. 2021)
DLC then lays the hammer down on the fact that gp41 is responsible for the dementia of AIDS.
I’m including the whole thing here.
Pathology:
Accumulation of β-Amyloid Precursor Protein in Axons Correlates with CNS Expression of SIV gp41 (2002)
“In this study, a strong association (p = 0.005) was identified between elevated axonal β-APP levels and the amount of SIV gp41 present in white matter, implicating HIV/SIV gp41 as a mediator of axonal damage.“
Mechanisms and Structural Determinants of HIV-1 Coat Protein, gp41-Induced Neurotoxicity (1999)
Abstract
Of the individuals with human immunodeficiency virus type 1 (HIV-1) infection, 20–30% will develop the neurological complication of HIV-associated dementia (HAD). The mechanisms underlying HAD are unknown; however, indirect immunologically mediated mechanisms are theorized to play a role. Recently, the HIV-1 coat protein gp41 has been implicated as a major mediator of HAD through induction of neurocytokines and subsequent neuronal cell death. Using primary mixed cortical cultures from neuronal nitric oxide synthase (NOS) null (nNOS−/−) mice and immunological NOS null (iNOS−/−) mice, we establish iNOS-derived NO as a major mediator of gp41 neurotoxicity. Neurotoxicity elicited by gp41 is markedly attenuated in iNOS−/− cultures compared with wild-type and nNOS−/− cultures. The NOS inhibitor l-nitroarginine methyl ester is neuroprotective in wild-type and nNOS−/− cultures, confirming the role of iNOS-derived NO in gp41 neurotoxicity. Confirming that iNOS−/− cultures lack iNOS, gp41 did not induce iNOS in iNOS−/− cultures, but it markedly induced iNOS in wild-type and nNOS−/− cultures. We elucidate the region of gp41 that is critical for iNOS induction and neuronal cell death by monitoring iNOS induction with overlapping peptides spanning gp41. We show that the N-terminal region of gp41, which we designate as the neurotoxic domain, induces iNOS protein activity and iNOS-dependent neurotoxicity at picomolar concentrations in a manner similar to recombinant gp41 protein. Our experiments suggest that gp41 is eliciting the induction of iNOS through potential cell surface receptors or binding sites because the induction of iNOS is dose dependent and saturable and occurs at physiologically relevant concentrations. These data confirm that the induction of iNOS by gp41 and the production of NO are primary mediators of neuronal damage and identify a neurotoxic domain of gp41 that may play an important role in HAD.
“I wouldn’t let these clowns dispense aspirin, let alone design fast tracked vaccines.“
Is gp41 a danger? It may well be. And nobody is asking the question, because (IMO) the neural pathogenic initiator that gp41 is, was passed off as a “molecular clamp” instead of the REAL ANTIGEN.
If they’re going to resurrect this weirdo COVID-HIV vaccine – and YES, they’re thinking about it – then there needs to be some examination FIRST of what the HELL is going on.
So What The Heck Is Going On Here?
When I was a young lad in the old days of science, there was lying, misrepresentation, and thievery, but it was on a much smaller scale.
We used to joke very cynically, back in the ’70’s, that every natural product being synthesized in a laboratory cured cancer, because we all knew that was not true.
We knew that these substances were really being synthesized merely because the molecules were a synthetic challenge, and a way for professors to make a name for themselves in synthetic chemistry. Almost NONE of these substances would EVER be used to treat cancer, and most would wash out very soon upon investigation. Almost none of them would ever even LEAD to a useful cancer drug. But LYING about their importance was how people got money for their labs. Every structurally interesting new molecule was always the next savior – until it wasn’t.
I used to think that the people giving out the money were fools about this, but not any more. I am beginning to think that the “givers” have always been just as corrupt as the “takers” – they’re just the “insiders” who turn on the spigots for their fellow “outsiders”.
I have no reason to think that vaccines are any different.
I think that a false crisis was used as a massive MONEY-BOMB – a global pile-on of the giddiest and most corrupt kind.
Probably the biggest one in 20 years.
I think that an AIDS vaccine was passed off as a COVID vaccine, by plausibly passing off the natural function of the HIV subunit as a new tool for other things, because – well – it IS such a new tool – just like every new interesting molecule MIGHT actually be some amazing new drug that cures cancer.
They lie skillfully, and they lie with truth, and it’s almost impossible to PROVE that the secondary “oh by the way” was actually the primary motivation.
We have changed from white lies that everybody understood WERE lies, to much more devious lies where scientists engage in fooling not just the public, but even other scientists.
I do think we have to wake up now. We can no longer afford the luxury of pretending not to know.
If I have to thank Joe Biden and his puppetmasters, including his “handler” Obama, for anything, it is for WAKING ME UP with these stupid mandates.
Nothing worked so well, to show us that the NEW WORLD ORDER is a direct threat to humanity, and needs to be stopped.
Science can be good again. But it must never, ever, abandon TRUTH.
While our beloved REAL bartender takes a needed break of unknown duration, we continue to ENDEAVOR TO PERSEVERE.
Christmas Spirit
We still have lights up all over the area. LOL!
Hey – how about we just keep believing?
And now, the rules of the pub.
HOUSE RULES
God bless us, every one! Tiny Tim had such a beautiful soul. He hadn’t a mean bone in his body…unlike most of us. But in keeping with Christmas, we promise to honor Wolf’s rules and keep Scrooge at bay. The Utree is where the Ghost of Christmas Present will conduct you should you need to rattle some chains. Another option, should all hell break loose is here.
Now, back to business.
AMEN!
Free the January Brothers
(no matter what the SHANGHAI SLIDER says)
Current Art On The Wall
We ordered a crate of ivermectin from Mexico, and instead got a box of counterfeit paintings marked “L.A.”.
We’re selling the paintings to make enough back for a new order of ivermectin.
As a Gab Pro member, I just got an email about the opening of the Gab Marketplace, which is now best described as a rudimentary “Gbay” precursor, using Gab Chat (the integrated version, not the end-to-end encrypted one) as the negotiating mechanism.
Here are some exemplary screenshots. Click on them to enlarge.
The landing page…..
Electronics…..
Beauty…..
There are no bells and whistles now, but the goal is to soon integrate GabPay, their PayPal substitute that has been under development for some time now.
Here is the text of the email.
Introducing the Gab Marketplace, a giant leap forward for the Parallel Economy on Gab!
GabPRO members can create listings for a variety of categories including books, electronics, tools, home goods, and more.
Anyone can view Gab Marketplace listings, ask about its availability, and chat with sellers to buy their items.
The Gab Marketplace can also be explored without having a Gab account and listings can be shared anywhere.
Gab does not handle transactions for Marketplace listings yet, but we will be integrating GabPay, our Paypal alternative, once it is live.
Sellers and buyers must converse amongst themselves regarding purchasing listings. We have many different categories and listings are filling up quickly, be sure to check back often to see new listings added.
We’ve also created a Job Board and Classifieds section in the Gab Marketplace.
Sell those electronics you haven’t used in forever, sell that Christmas gift you never opened, or anything in-between!
We have seen some of these already, alleging things like “pandemic stress” being responsible for clot-shot cardiac consequences. Those were bad, but now it’s just becoming ludicrous.
It’s very clear to me that the “Fake News” has been tasked with trying to GET PEOPLE TO INNOCENTLY RATIONALIZE the downstream effects of the FAILED plandemic and clot shot plot, whatever those might eventually be proven to have involved.
Trump really tried to get people to see the MEDIA ROLE in regard to “climate change” – that CLIMATE ALARMISM was basically a SIMULTANEOUS media hoax on both scientists and non-scientists.
As long as the media will defend the LIE that science itself, individual scientists, and scientists as a group, are ALL in full, 100% control of what they themselves think, then the TRUTH that the media controls what science thinks and says can be hidden from the public.
It is only NOW – at a moment when many scientists are WAKING UP to what the media has done TO THEM, and are actively TURNING IT OFF, that they realize the media was LEADING THEM.
Let me state this clearly.
FAKE SCIENCE – controlled by the media – is one of the greatest dangers to humanity EVER.
FAKE NEWS is used to lead Fake Science – to hint subconsciously to science and scientists where it’s “going”.
FAKE ENTERTAINMENT is used to normalize Fake Science – to raise the barriers to questioning it.
IT IS YOUR DUTY TO PERCEIVE AND REJECT FAKE SCIENCE.
Being moderately scientifically literate is now a SURVIVAL SKILL, just like being politically literate, or even being just plain literate.
We will continue to bash fake science here, and I personally will continue to appreciate all examples of it that you may find and bring here, because dissecting and analyzing fake science is one of the best ways to fight it.
REAL SCIENCE is making a comeback, and YOU, DEAR AND PATRIOTIC CITIZEN, are part of that GREAT AWAKENING.
Malone and Bhakdi Validated by “Pro-Vax” Paper
On Monday, I covered a recent paper coauthored by Dr. Peter McCullough, which hypothesizes that documented failure of the mRNA vaccines to activate the interferon system, in combination with documented migration of both vaccine-induced spike protein and specific interferon-suppressing microRNAs via exosomes, is behind a variety of health problems associated with the current COVID vaccines.
The hypothesis of this paper is based on rough but obvious signals from VAERS, existing mRNA vaccine data in the literature (interferons and related species, microRNAs, exosomes), and known mechanisms which would explain the VAERS signals if connected to the vaccine data.
I was only partway through that paper, when I was saying to myself “Good grief – why are we even USING these vaccines, much less mandating them?”
Now, as a kind of second strike, Malone has found a paper which not only confirms his suspicions and fears of mRNA vaccine problems, but which also perfectly confirms Dr. Sucharit Bhakdi’s contention that the mRNA vaccines are producing too much of the WRONG antibody type and none of the two more desirable types.
Let me cite the beginning of this post – up to where Malone poses the big question.
A Health Public Policy Nightmare
Vaccine spike antigen and mRNA persist for two months in lymph node germinal centers… protein production of spike is higher than those of severely ill COVID-19 patients!
Vaccination confers broader IgG binding of variant RBDs than SARS-CoV-2 infection
Imprinting from initial antigen exposures alters IgG responses to viral variants
Histology of mRNA vaccinee lymph nodes shows abundant germinal centers
Vaccine spike antigen and mRNA persist for weeks in lymph node germinal centers
The hidden highlight (lede) buried in this peer reviewed paper is that protein production of spike in people vaccinated with the Moderna or Pfizer vaccine is higher than those of severely ill COVID-19 patients! A person might ask, “How could that be?” In order to understand this, we must carefully analyze what the study shows.
I urge you to finish reading Malone’s post about this paper.
I ALSO urge you to read the paper itself (PDF is public), which looks at the same data, and cheer-leads vaccines, stating but otherwise ignoring EVERYTHING that Malone and Bhakdi are concerned about. Ignore the parts you can’t read – there’s plenty that you CAN read, and it is very instructive.
I will attempt to explain the difference between the two views of the same results, but let me give you the Bottom Line Up Front (BLUF).
The original paper was researched and written while the participants were fully under “Gates Vaccine Mind Control” and “Fauci Antibody Hypnosis”, both of which cause scientists to rather blindly follow the laser-pointers which control their outlook on vaccine science.
Gates: Vaccines are the only legitimate way to fight viral disease.
Fauci: Antibodies which I designate determine if a vaccine is safe and effective.
These are the lies of SMART SCIENCE LIARS, because they’re difficult to prove untrue in a way that normies can understand.
As Robert Malone notes, one of the most important facts in the paper [that the vaccines produce more spike protein than even severe cases of COVID-19] is a “buried lede”, although I would go further and state that it was never buried, because it’s not even a concern to the authors.
Once one accepts a priori that:
vaccines are good
vaccine side effects are obvious, immediate, and allergic in nature
spike makes antibodies, and antibodies are good
concerns about the spike protein are misinformation
…..then it is pretty much impossible for these COVID vaccines to do any wrong.
Just ask a scientist, who believes all these things BECAUSE OF THE MEDIA.
More spike protein means more antibodies, and more antibodies is good – RIIIIIGHT?
And if there are problems, it’s the vaccine working! Just ask Jabcinda Ardour!
ANTIBODY HYPNOSIS WILL DO THAT. Under antibody hypnosis, anything which contributes to antibodies which Fauci highlights, is “good” – all other antibodies or other responses are either bad or irrelevant.
The authors of the paper make sure to say all sorts of good things about vaccines, and never say anything critical, despite the fact that they’re sitting on all kinds of evidence that something is very wrong with these mRNA vaccines.
Example:
The appearance of virus variants, waning antibody levels after infection or vaccination (Falsey et al., 2021; Levin et al., 2021), and breakthrough infections in previously immunized individuals (Keehner et al., 2021) indicate that periodic vaccine boosting of immunity to SARS-CoV-2 is warranted.
REALLY? Some of us scientists believe the exact opposite – that these diverse FAILURES indicate that a vaccination strategy is dubious if not highly UNWARRANTED – but OUR view is called “misinformation”.
Seriously – it’s like hypnosis. The authors of the paper CANNOT SEE the things that Malone points out, or that Bhakdi pointed out.
Likewise, the problems which WE can see were clearly NOT found in “peer review”, precisely because the PEERS are for the most part just as much under vaccine hypnosis and antibody hypnosis as the authors, so real and deep questions about the jabs are simply never going to get asked. And if any peers DO recognize the problems, they will keep their mouths shut, or “test the waters” gently, to see if any concerns are allowed.
Those who CAN see the problems, know enough to keep their mouths shut, if they want to remain players in the Science Game.
I go back to what I said earlier about the media – including the science media – including journals – literally CONTROLLING what scientists think – and that scientists have no clue. Sad.
Anyway, now that I’ve provided background of what is going on here – a “pro-vax” paper in which Malone finds shocker evidence of problems, let’s discuss the specifics that Malone found, and that Bhakdi also predicted.
One of the first things that Malone catches is the persistence of both the mRNA and the spike protein in lymph node germinal centers – lasting for WEEKS instead of a few days. Note that this perfectly matches a clinical case that we featured here on these pages!
I have here an absolutely fascinating video (end of article) from Gab TV that fits right into everything I know about COVID-19 and the spike protein vaccines, like the last piece of a puzzle. The video is just under 1/2 hour in length, but it is FILLED with little AHA moments. An extremely articulate, healthy, …
Basically, this woman (on the left) got “long haul COVID” symptoms from a JAB – including massively swollen lymph nodes that lasted for WEEKS. That led to a lot of permanent damage. What she experienced is now explained PERFECTLY by what Dr. Malone postulates.
AND I NOTE THIS AS WELL. What Dr. Malone postulates (below), is exactly what The Ethical Skeptic noted as a CONCERN on Twitter in 2020, before the vaccines ever arrived! Yes, I have not gone looking for his tweet, but TES specifically noted that these vaccines are not “actual” mRNA vaccines – they are PSEUDO-mRNA vaccines.
WHUUUUUUUUT?????!!!!!
Yes. To evade immune protection from foreign mRNA, the vaccine mRNA uses a “pseudo” base to trick the human immune system into thinking it’s not mRNA, even though it works the same way. It’s something of a beautiful hack, but it’s a hack.
Malone:
One very real hypothesis is that the substitution of pseudouridine for uridine to avoid the immune response is working so well that the mRNA is completely evading the normal clearance/degradation pathways. Hence, mRNA that is not being incorporated into cells at the injection site, is migrating to the lymph nodes (and throughout the body as the non-clinical Pfizer data suggest?) and continuing to express protein there. In this case, the cytotoxic protein antigen is spike. Spike protein can be detected for at least 60 days after administration of dose. Note that the duration of the protein expression was only tested for 60 days.
But it gets worse. After reminding us of the pathogenicity of the spike protein (merely citing others), Malone reminds us that the use of pseudouridine to evade immune cleanup is not actually necessary in mRNA vaccines – but it IS (and this is rather horrible) PATENTABLE as an “improvement”.
Again, Malone.
To note: The use of pseudouridine in these mRNA vaccines is not the only option. It has often been hypothesized that the reason Dr. Kariko added pseudouridine to the mRNA vaccine was to make an improvement to the original mRNA patents that I was an inventor on. An improvement to an existing patent allows commercialization of that patent. It is an old trick. Remember, that Curevac does not use pseudouridine in its formulation and it is not required or necessary for a significant immune response. In the next generation of mRNA vaccine experiments (hopefully done in an animal model), it is clear that the issues of adding pseudouridine need to be addressed prior to any more of these vaccines going into humans.
So how much spike protein does this stuff produce? Again, Malone.
Knowing what we know about the spike protein in these vaccines, the study quantitatively measured spike protein levels in plasma after vaccination. Which, it turns out, are higher than the levels observed in a person with a severe COVID-19 infection. Just to write it, the fact that this only now being discovered or it it was known, released to the public is criminal in my opinion. This should have been characterized long ago, including prior to beginning human clinical trials.
That this has not been published or investigated more demonstrates the gross regulatory dereliction of duty by Pfizer, Biointech, Moderna, NIAID VRC and that whole crew. Using these vaccines, which include pseudouridine without fully understanding the implications and without the FDA requiring a complete pre-clinical toxicology regulatory package, including long-term follow-up, as is done with any other unique chemical or adjuvant additive is shocking. Then there is the novel use of the unique nano particles being used in these vaccines, which also were only marginally assessed, as shown by the Japanese Pfizer data.
Protein expression is not being turned off, because the immune response against the mRNA/pseudouridine complex is either not happening or is ineffective. It may also be that the mRNA/pseudouridine complex has a longer half-life than normal mRNA. The In either case, this is regulatory nightmare.
I do not know how to write this more strongly. This technology is immature. The WHO has approved six, more traditional vaccines, all of which the US government could license. These genetic vaccines are not the only option.
And just to make sure you get it, Malone quotes the relevant parts of the paper, and says it again.
Read that again: Protein production of spike is higher than those of severely ill COVID-19 patients!
As an understated closer, without mentioning him by name, Malone adds how THIS paper confirms a concern that Dr. Sucharit Bhakdi had about THE WRONG ANTIBODY TYPES being produced by the vaccines.
The paper also notes that the antibody response is IgG, not IgA or IgM. IgA and IgM antibodies produce a strong mucosal immune response needed for respiratory diseases, unlike IgG.
Finally, Malone makes this statement.
This Substack article has only skimmed the surface of the implications of this paper in terms of both the science and the malfeasance on the part of our government and pharmaceutical corporations. There is more to come on this issue.
You will note that, by implication, the AUTHORS of this paper clearly said nothing indicative of malfeasance. Now it may be entirely possible that they were “getting out truth” while keeping their heads out from under any funding guillotines, but they clearly evidenced no overt concerns for any problems.
And THAT is how FAKE SCIENCE works, my friends.
Lastly, let me add one of my own “concerns”.
Allow me to repeat the authors’ own highlights of the paper, for commentary.
Vaccination confers broader IgG binding of variant RBDs than SARS-CoV-2 infection
Imprinting from initial antigen exposures alters IgG responses to viral variants
Histology of mRNA vaccinee lymph nodes shows abundant germinal centers
Vaccine spike antigen and mRNA persist for weeks in lymph node germinal centers
To these FOUR items, I have FOUR responses, all of which I know Karl Denninger will get.
Leaving aside IgG being the wrong antibodies (see above), BINDING antibodies can still, also, be “wrong” (or more accurately “inappropriate”) antibodies, depending on what happens next, including enhanced variants and ADE. NEUTRALIZING antibodies are the “most appropriate” kind. BINDING antibodies may or may not help. So DO NOT take this point as an automatic score for the vaccines. In my humble opinion, NATURE is likely smarter than Pfizer and Rochelle Alinsky on what to do here.
Original antigen sin. They’re calling it. “Imprinting.” It means that every exposure to an antigen can potentially MISLEAD the immune system for the purposes of the next exposure. Great. SO – how confident are you folks that these vaccines are giving a superior “imprinting” to natural infection? I am NOT confident, and in fact, I believe that the “pseudouridine error” is proof that NIH, Pfizer, Moderna, CDC, CEPI, and all the rest are not even remotely competent to choose the best “imprinting” for children. They are choosing the one that gives themselves the most power, control, and money. SHAME!
The vaccines are going to the lymph nodes. Well, well, well. Not only does this destroy the establishment TROLL talking point about vaccine localization in the deltoid muscle – it provides a nice explanation of the exosome-based spread of the spike protein and interferon-suppressing microRNAs.
Persistence of vaccine and thus-produced spike in the lymph nodes lasts for weeks. Add to this the liberation of spike protein in LIPID-BASED EXOSOMES into the bloodstream. What’s that going to do? Why, it’s going to SPREAD SPIKE IN LIPIDS to other places where lipids collect. Which means spike ends up in other organs. Which can potentially include organs (like skin and other glands) which SHED LIPIDS. Which includes breast milk (dead infants in VAERS) and skin oils (see prior posts on this blog, where my incredulity about “shedding” was overcome). AND don’t forget the ovaries. Etc.
So – that is where we are.
And where is Fake News on this? Totally absent.
We’re not only the news now.
We’re the science now.
ENJOY THE SHOW.
Thank you all for being here. Have a great weekend.
PREMIERE 10/25 at 7:30pm ET on 
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