“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
We are NOT serving mercurials or arsenicals today – or EVER – but we ARE serving MODERN SUBSTITUTES like penicillin – to the non-allergic, of course.
While our beloved REAL bartender takes a needed break of unknown duration, we continue to ENDEAVOR TO PERSEVERE.
Christmas Spirit
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 have a really RETRO shipment this week. All designed to go along with our FEATURE PRESENTATION.
These are presented in the order that they came out of the box.
PATENT MEDICINE PILL, 1890.
Advertisement for Beecham’s Pills from an American newspaper of 1890.
Interestingly, Beecham’s Pills were actually USEFUL. They contained aloe, ginger, and SOAP, the latter meaning that they were much like stool softeners – a gentle laxative.
Not so sure about snake oil…..
The following is a subtle ad for CHILD DEWORMERS.
With this picture, we begin some ads for Dr. D. Jayne and his products. His company lasted for around a century. He was an actual trained doctor, and tended to use pharmaceuticals with real physical effects, like digitalis, opiates, etc., rather than quack ingredients.
American children tended to have roundworms and pinworms – Dr. Jayne’s “vermifuge” apparently worked on both.
Jayne used a lot of artwork in his marketing – thus many of his product advertisements can still be found.
The following is very subtle propaganda.
Jayne’s was still around as WWII loomed. Many of our childhoods were not long after this. Bear this in mind later in this post.
More “Jayne’s art”.
The expectorant apparently contained ipecac, opium and digitalis.
Nothing like a good salve!
Stabler’s apothecary was run by multiple generations of a family of pharmacists. The founder, Edward, was an interesting herbalist, trained in Pennsylvania. He was an abolitionist in Virginia who would purchase slaves to set them free. http://www.connectionnewspapers.com/news/2006/feb/01/herbal-remedy/
I hope you have some idea now about medicine in the 19th century.
Do you think we’ve advanced much?
Let’s move “forward” now, to “state of the art” 19th century prescription medicine.
Seatbelts.
Mercury and Arsenic as the mRNA and Remdesivir of Pre-Fauci America
In the process of reading about how COVID vaccines are now setting off syphilis tests (a topic which we covered last Friday), I chanced upon a boatload of information about early treatments of syphilis, and what I read simply blew me away.
The scandals of syphilis are WAY, WAY more than the “shame of the disease itself”, and WAY, WAY more than the Tuskegee syphilis experiment.
These scandals are SMALL POTATOES compared to the scandal of TREATMENT OF SYPHILIS WITH MERCURY.
This is history you will NOT learn under globalists and progressives.
A scandal which was SO BAD – just like “treatment” with these demonic mRNA vaccines – that medicine started QUIETLY – without admitting fault – looking for an exit strategy. And part of that was motivated by this fact:
BLACKS and other groups who were not getting “treated” with mercury, were not suffering many of the WORST end-stage “symptoms of syphilis”.
You see what I mean? It was JUST LIKE THE CLOT SHOT. Just like remdesivir. BLAMECASTING the errors of the BAD but moneymaker treatments onto the disease.
This is NOT NEW STUFF.
In fact, it is MOST IRONIC that the Tuskegee experiment STARTED OFF by literally SAVING the participants from treatment with mercury – only to then DENY THEM penicillin when that became available, so that they could continue the experiment.
Because the experiment was not merely about “not treating people”.
It was REALLY about NOT TREATING PEOPLE WITH MERCURY.
And THIS explains why there was so much determination to get these participants to the end-stage WITHOUT TREATMENT. Because it was end-stage effects that they were so interested in observing.
What I discovered was that the history of medicine in America is FILLED with stuff every bit as bad as the DEMON Anthony Fauci, the disaster of AIDS and AZT, toxic drugs like remdesivir, and medical killers like the untested mRNA vaccines. Much of it is exposed by the history of syphilis, so that is where we will begin.
The Wikipedia article on syphilis doesn’t say much about the actual treatment of syphilis with mercury, despite it having a fairly extensive section on treatment. A much better coverage is found in the article on the History of syphilis.
However, even THAT does not really give you a sense of the magnitude of what might gently be called “the problem of mercury as a medicine”.
Let me put it this way. When it turned out that MALARIA and ARSENIC were both superior and more importantly SAFER treatments of syphilis relative to the “consensus treatment” of MERCURY, you know that mercury was BAD SHIT as a medicine.
Obviously, if they tried MALARIA and ARSENIC, people KNEW that mercury was a bad drug.
In fact, I was shocked to find that the current confrontation between “natural therapies” and “pharmaceuticals” is a VERY old conflict that never went away. While there has been SOME reduction in the mortality difference between “do no harm, save a few” natural remedies and “kill a bunch of people, save a few” pharmaceuticals, we are still talking about millions of Americans killed by pharmaceuticals intended – or maybe just “purported” – to save them.
Anyway, here is the big picture.
The “clot shot” and the people who maliciously pushed it are entirely believable in the long, dark shadow of “killer calomel”.
SO – let’s get started with Hg2Cl2.
My parents actually had a bottle of calomel (not calamine – the neighbor kids had that) in the medicine cabinet when I was a kid. It was somewhat more modern than the above, with a metal screw-cap. Indeed, my parents had a lot of very old-school medical stuff from the 40s and 50s.
As children, we treated all our wounds with the mercury compound thiomersal, a.k.a. merthiolate. You know – the bad stuff in vaccines. This is the “new” bottle which I loved – we had older glass bottles with a glass dipping rod, before these handy squeeze bottles.
Calomel has a LONG history as a therapeutic. Although it got its start back in alchemy, by the time it got to America, it was a common medicine.
From Wikipedia:
By the 19th century, calomel was viewed as a panacea, or miracle drug, and was used against almost every disease, including syphilis, bronchitis, cholera, ingrown toenails, teething, gout, tuberculosis, influenza, and cancer. During the 18th and early 19th centuries pharmacists used it sparingly; but by the late 1840s, it was being prescribed in heroic doses[7]—due in part to the research of Benjamin Rush, who coined the term “heroic dose” to mean about 20 grains taken four times daily.[8] This stance was supported by Dr. Samuel Cartwright, who believed that large doses were “gentlest” on the body.[9] As calomel rose in popularity, more research was done into how it worked.
J. Annesley was one of the first to write about the differering effects of calomel when taken in small or large doses.[9] Through experimentation on dogs, Annesley concluded that calomel acted more like a laxative on the whole body rather than acting specifically on the vascular system or liver as previous physicians believed.[9] In 1853, Samuel Jackson described the harmful effects of calomel on children in his publication for Transactions of Physicians of Philadelphia.[7] He noted that calomel had harmful effects causing gangrene on the skin, loss of teeth, and deterioration of the gums.[7] On May 4, 1863, William A. Hammond, the United States’ Surgeon-General, stated that calomel would no longer be used in the army as it was being abused by soldiers and physicians alike.[7] This caused much debate in the medical field, and eventually led to his removal as Surgeon-General.[10] Calomel continued to be used well into the 1890s and even into the early 20th century.[7] Eventually calomel’s popularity began to wane as more research was done, and scientists discovered that the mercury in the compound was poisoning patients.
Calomel was the main of the three components of the pill number 9 of the British army during the First World War. [11]
But if you REALLY want to understand the history of calomel as both a poison and a drug, this is the article you need to read.
This article totally gets it, as you can tell from the opening quote.
New drugs present greater hazards as well as greater potential benefits than ever before—for they are widely used, they are often very potent, and they are promoted by aggressive sales campaigns that may tend to overstate their merits and fail to indicate the risks involved in their use. . . There is no way of measuring the needless suffering, the money innocently squandered, and the protraction of illnesses resulting from the use of such ineffective drugs.
John F. Kennedy, in his Consumers’ Protection Message of March 15, 19621
Is the whole “Q” thing starting to make sense? Just as an aside. JFK clearly had some of the same enemies as Trump.
Anyway, this article shows how the use of mercury and arsenic compounds for medicines was controversial even from the START, with Paracelsus himself admonishing fellow alchemists not to use too much mercury in treatments.
The problem with calomel is that it’s insoluble MOST of the time, and in that state it can be used in excess, because it just flushes through the body. It’s a lot like barium sulfate – a totally safe version of highly toxic barium – in that respect. But if calomel oxidizes, or becomes impure, or otherwise emits other forms of mercury, it can be very harmful.
Thus, calomel got good results in some hands, but in the hands of other physicians, and in the bodies of other patients, it was a killer. It was easily abused, and even some of the “megadose” treatments were abusive from the git-go – to say nothing of giving it to children, and doing life-long damage.
But now, let’s look at what calomel and other mercury compounds did for syphilis. For THAT we go to another great article.
This article does a deep dive on use of mercury to treat syphilis, and does not hold back on the contention that much of the symptomology of syphilis that was seen before penicillin, was really due to mercury poisoning and NOT due to syphilis itself.
Sound familiar?
This article in particular contends that the end-stage dementia of tertiary syphilis in the West, which was observed much less frequently in certain populations like blacks, Indians, and Norwegians, who avoided mercury, was mostly due to the treatment with mercury, not syphilis.
In case you’re thinking that’s unlikely, just consider patient-killing remdesivir, which we’ve covered extensively.
Now, there IS an great academic look at the skeletons of syphilitic patients, some of whom were treated with mercury, trying to determine if mercury made things worse. The results are inconclusive, but in any case, the background material is excellent reading.
More Harm than Healing? Investigating the Iatrogenic Effects of Mercury Treatment on Acquired Syphilis in Post-medieval London.
Molly K. Zuckerman
DOI 10.1515/opar-2016-0003 Received October 26, 2015; accepted March 29, 2016
Abstract: Mercury was commonly used to treat syphilis in post-medieval Europe, but debate persists about whether it ameliorated infection or exacerbated it. As there are no in vitro studies on mercury’s effectiveness, Hg levels were characterized using an established technique, portable X-Ray Florescence Spectrometry (pXRF) in syphilitic skeletons (N=22) from six post-medieval London cemeteries. Levels were assessed against proxies for syphilitic infection severity (lesion type, episodic involvement, extent of involvement), oral health indicators, and age at death. The findings are equivocal, likely obfuscated by background poor oral health and high mortality, and cannot elucidate whether mercury ‘killed or cured’.
Keywords: syphilis, mercury, pXRF, post-medieval, London, trace element analysis, paleopathology.
The history of treatment with mercury in America serves as a strong precedent for what we are seeing now with “vaccines for everything”. The mendacity of some and the fecklessness of others regarding COVID treatments is not new – it all happened before with the mendacious and feckless medical establishment – and MERCURY.
And just for my fellow lovers of history-of-science porn, click on the following for the full-sized image.
From Wikipedia.
L0057102 Mahogany medicine chest, England, 1801-1900
Credit: Science Museum, London. Wellcome Images
images@wellcome.ac.uk
http://wellcomeimages.org
The mahogany medicine chest contains boxes, bottles and tubes of medications to treat a number of conditions. The chest includes treatments to purge the body by vomiting (emetics), by sweating (diaphoretics), as well as general purgatives such as rhubarb, jalap and calomel. Other medications include pain relief, such as opium plus astringents and stimulants, including ginger and lavender. The chest contains a handwritten inventory listing the medications. The chest also includes a set of scales, weights, a pill tile and a spatula. The set was probably used in the home or by a chemist or apothecary.
maker: Unknown maker
Place made: England, United Kingdom
made: 1801-1900 Published: –
Copyrighted work available under Creative Commons Attribution only licence CC BY 4.0 http://creativecommons.org/licenses/by/4.0/
And don’t forget to…….
ENJOY THE SHOW.
Thank you all for being here. Have a great weekend.
Get your rest, Trumpy Bear! You’re needed in WASHINGTON, DC!!!
Vladdy Bear and Winnie The Pooh are making Sleepy Creepy Joe look like a punching bag!
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’re ON A ROLL.
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.
Gonna be quick this time.
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.
After his speech at CPAC, I think it’s quite clear that praying for President Trump’s return to the White House is indeed praying for our enemies, who are too messed up to realize how much better off they would be under a Trump presidency.
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.
Microwave Monday reminds me of this song from back in the day.
ENJOY!
This right here is the stiffest dose of teased-out 80s chick hair you are EVER going to get.
And if you want to see it with 2008 hair….
And then there’s an outdoorsy 2014 version which has a really great “live” feel…..
But how about a 2021 version with just Susanna Hoffs and a string section?
But if you’re still feeling like it’s all unfamiliar, here’s the original video!
Yeah – that’s more like it!
Call To Battle (H/T Sundance)
Our beloved country is under Occupation by hostile forces.
Daily outrage and epic phuckery abound.
We can give in to despair…or we can be defiant and fight back in any way that we can.
Joe Biden didn’t win.
And we will keep saying Joe Biden didn’t win until we get His Fraudulency out of our White House.
…..and now for…..
Microwave Monday
After recent discussion of Havana Syndrome, and the possibility that it involves electromagnetic radiation (and in particular microwaves), I have decided that we all need to LEVEL UP our gut-level understanding of the electromagnetic spectrum – even beyond what Steve has done with his explanation of the science behind it.
This will also help us deal with both the REALITIES and DISINFORMATION of 5G telecom.
I will be doing this by giving you all a bunch of INFOGRAPHICS to get started.
Steve got us started HERE, in his 8th science lesson on LIGHT.
You may remember some of this stuff….. (CLICK TO ENLARGE)
Let’s start breaking up that electromagnetic continuum into REGIONS that have NAMES.
You can see that microwaves lie between RADIO and INFRARED.
Let’s look even more closely at those groups.
We can even start breaking those radio and microwave regions down into BANDS that you are all familiar with.
Here you can start to get a feel for the SIZE OF THE WAVES versus objects and frequencies.
The SIZE OF WAVES and WHAT THEY AFFECT actually matters – although it’s not simple.
Megahertz, gigahertz, teraherz, and petahertz are all there.
You can really see it more easily in the following infographic.
You can easily see how we have made “radio devices” push farther and farther away from the very SAFE “radio” region, through television, mobile phones, and WiFi, closer and closer to the microwave and infrared radiation that constitutes COOKING MICROWAVES and RADIANT HEAT ITSELF.
And as you can see here, many technologies emit electromagnetic radiation – and some more than you may have realized.
So where are the 5G frequencies? Please be aware that there is constant change in this stuff, so that these infographics may be slightly out of date. Do not let that deter you – minor changes don’t NIX any issues of the basic range in which 5G operates, unless specifics of the science are given.
Use COMMON SENSE.
Let’s zoom in a bit.
Note that the above is just the US – other countries use different regions.
Here is more detail on European and US 5G.
Much of this is SQUARELY in the microwave region. From Wikipedia, we’re basically talking 300 MHz to 300 GHz.
Now let’s start looking at ALLEGED but possibly REAL health effects of EMR in the microwave region, which may VARY ACROSS THE REGION.
Remember also that DOSAGE MATTERS – like anything else.
You have to squint to see the next infographic, but look at “Biological Effect”.
It depends strongly on FREQUENCY / WAVELENGTH.
This is a very good listen. This lady is also a climate dupe, but she will get you to realize that your microwave devices may actually be doing to YOUR MEAT what microwaves normally do to YOUR MEAT, albeit at LOWER BUT LONGER DOSAGES.
This is another good one!
More of her schtick. This gal will get you to question the “harmless” narrative, just like vaccines, but try to keep some common sense. Remember – driving is a killer, too. You still want the freedom to drive?
Common sense! How do we get the BEST of both worlds?
Now I’m just going to play a bunch of their infographics. Caveat emptor! But some of this stuff is interesting and counter-intuitive. SIGNAL and NOISE matter. In more ways than one.
SO – maybe you should THINK about how to handle the devices you have!!!
But then talk back to all that stuff HERE.
Be sure to be SKEPTICAL of this SKEPTIC lady – that is an essential part of ETHICAL SKEPTICISM. We don’t want to be panicky about 5G, or believing disinformation, but we do want to treat MICROWAVES as maybe not that awesome for our health, in doses that exceed our individual sensitivity.
So BEWARE of BROAD-BRUSH SKEPTICS who downplay too much in favor of technology.
After all, we just got through a BATTLE ROYALE over disastrous mRNA technology that was advanced too fast for all the wrong reasons.
Finally, a GREAT infographic. It’s MASSIVE. I’m only showing you the small version – you have to click the link for the BIG ONE that’s easy to read down to the details.
Something stinks, and to my nose, it’s the New World Odor.
But first, a disclaimer.
I’m actually ashamed that I wanted to work for Google at one point, but I need to get that out into the open right away, lest somebody, someday, use that “gotcha” against me and think it’s actually damaging.
Heck – I even bought a variety of Google swag, back when they were small and upstarty, just like when Netscape, Firefox, various Linux brands, and other rising tech companies were once “new” and “cool”.
A lot of people once thought that Google’s motto of “Don’t be evil” was a bit of a bass-ackwards under-performer, which should have been a positive, rather than a double-negative. Not me. I realized back then that this paradoxical formulation was exactly why the motto was so ahead of the curve.
“Being good” lacks skepticism – particularly of self. “Being good” as a primary motivator is a guaranteed set-up for the primary sin of PRIDE.
“Not being evil”, in contrast, is automagically skeptical of self. And skepticism isn’t just good for science – it’s good for religion.
Yes – I think it’s clear you need both. This is part of why (IMO) Christianity always refreshes itself by going back to its Jewish roots when there are foundational questions. No matter how you slice it, we need to concern ourselves with the Law, which includes consequential negatives, because we don’t want to get rid of our saving prohibitions.
We need our Peters, but we also need our Pauls.
Thus, when Google ditched “don’t be evil”, I smelled trouble.
And what is happening now, may be evidence that Google has forgotten how to “not be evil”.
Google has made mistake after mistake since they began tampering politically with their search engine, largely during the Obama years, but to an even greater degree during the Trump years. And now, in one short year of Biden – Google has arrived at the point of adopting a policy that conflicts with the most basic principles of science.
Simone Gold, of America’s Frontline Doctors, just tweeted this.
WOW: @Google sent notice stating they will be removing the America’s Frontline Doctors website from search results.
We are a team of medical doctors who dared to speak the truth.
“Nor do we allow content from any site that contradicts or runs contrary to scientific or medical consensus and evidence-based best practices.”
Well THAT’S great. How do you think science is going to advance? YOU CHUMPS!
Let’s just save that tweet, simply to make sure that it doesn’t disappear when Twitter inevitably suspends Dr. Gold.
Note these final words from Dr. Gold.
“And we have been proven right, again and again, and again.“
Dr. Simone Gold, AFLD
Dr. Gold is not lying. Throughout COVID-19, free and independent doctors and scientists have been LEADING captive science and captive medicine against their BIASED FUNDERS AND CONTROLLERS – which clearly include GOOGLE now.
The “concensus” science has repeatedly and continuously been ABNORMALLY WRONG due to BIAS, and has required continuous correction by – very sadly – OUTSIDERS.
Science does not progress by sticking to consensus. It advances by CHALLENGE TO CONSENSUS. Google is INTERFERING with that process. SHAME!!!
In my opinion, “they” are all scared.
And the reason they’re scared it this.
Now – as insurance companies look around to see who picks up the tab for people dying from the ERRORS OF THE CONSENSUS, it sure ain’t gonna be able to pin it on the people who WARNED about the experimental vaccines.
It may indeed be that some of the blame (moral, even if not monetary) will land on those who CENSORED THE SAVING WARNINGS.
Over and over, people like Google censored us because they said that the things WE SAID were not true, and yet it turned out that the things we said WERE true, and that the consensus THEY said was true, was both WRONG and responsible for MANY DEATHS.
And THIS may be the biggest CENSORED TRUTH of all.
Alden et al, Lund University, Sweden, confirms one of our worst fears. The exogenous genetic material coding for the dangerous Spike protein is reverse-transcribed into the human genome; possible long-term constitutive expression/synthesis of disease promoting/lethal Spike. pic.twitter.com/JEzSwSruWM— Peter McCullough, MD MPH (@P_McCulloughMD) February 25, 2022
Here, I saved an image of a copy which was only partially destroyed by Twitter.
And here I saved the actual tweet (in two pieces).
Here is that image within the tweet, in more detail.
So what is McCullough talking about? And what is Twitter hiding?
Academic Editor: Stephen Malnick Curr. Issues Mol. Biol. 2022, 44(3), 1115-1126; https://doi.org/10.3390/cimb44030073 (registering DOI) Received: 18 January 2022 / Revised: 19 February 2022 / Accepted: 23 February 2022 / Published: 25 February 2022 (This article belongs to the Topic Clinical, Translational and Basic Research on Liver Diseases)
Abstract
Preclinical studies of COVID-19 mRNA vaccine BNT162b2, developed by Pfizer and BioNTech, showed reversible hepatic effects in animals that received the BNT162b2 injection. Furthermore, a recent study showed that SARS-CoV-2 RNA can be reverse-transcribed and integrated into the genome of human cells. In this study, we investigated the effect of BNT162b2 on the human liver cell line Huh7 in vitro. Huh7 cells were exposed to BNT162b2, and quantitative PCR was performed on RNA extracted from the cells. We detected high levels of BNT162b2 in Huh7 cells and changes in gene expression of long interspersed nuclear element-1 (LINE-1), which is an endogenous reverse transcriptase. Immunohistochemistry using antibody binding to LINE-1 open reading frame-1 RNA-binding protein (ORFp1) on Huh7 cells treated with BNT162b2 indicated increased nucleus distribution of LINE-1. PCR on genomic DNA of Huh7 cells exposed to BNT162b2 amplified the DNA sequence unique to BNT162b2. Our results indicate a fast up-take of BNT162b2 into human liver cell line Huh7, leading to changes in LINE-1 expression and distribution. We also show that BNT162b2 mRNA is reverse transcribed intracellularly into DNA in as fast as 6 h upon BNT162b2 exposure.
I have discussed the Jaenisch paper numerous times since I became aware of it in December of 2020, and more importantly in March of 2021.
In fact, in the following blog post I made in April of 2021, I actually hypothesized a scenario which is basically the findings of the De Marinis paper!!!
Alternate Title: Is Persistent Reverse Transcription a Hidden Virus/Vaccine Objective? Gloating Pre-Preface There are few feelings of satisfaction like opening up the NEWS and knowing one’s theories and understandings are WORKING even better than one thought. Let’s see if they use this one for damage control, and get the “new science” out before the STORY …
Now – let me state, in the simplest possible way, what these papers mean.
The Jaenish paper proves that the SARS-CoV-2 (COVID-19) virus alters human DNA.
The De Marinis paper proves that the Pfizer mRNA vaccine also alters human DNA.
Oh, there are quibbles that I’m “oversimplifying”, but they’re just quibbles, and I will show you WHY they are not just quibbles, but extremely disingenuous ones.
And please note that I am UNDERSTATING when I just say “alters DNA”. The Jaenish paper proves that the viral DNA changes are going into GENOMIC DNA. The De Marinis paper strongly suggests that THE SAME may be happening due to the vaccine.
But before I give you MY take on the De Marinis paper, let me give you the opinions of OTHERS.
Let’s review one first.
Peter McCullough:
Alden et al, Lund University, Sweden, confirms one of our worst fears. The exogenous genetic material coding for the dangerous Spike protein is reverse-transcribed into the human genome; possible long-term constitutive expression/synthesis of disease promoting/lethal Spike.
Translation: The pseudo-mRNA code for the spike protein in the Pfizer vaccine gets into the genomic DNA inside human cells in test tube experiments, and produces both DNA and mRNA coding for what was uniquely in the vaccine. This new cellular DNA and RNA very likely (as a consequence) produces spike protein, causing long-term disease and health issues.
One can legitimately contest the assertion that genomic DNA is being altered (we don’t know this yet – hopefully soon), but any denial of the fact that CELLULAR DNA is being changed, is simply not “fact-based”.
For example, I saw “downplay trolls” on the original McCullough tweet, quibbling about in vivo vs. in vitro – that these results don’t “prove” that the same thing happens in living humans – only in living human cells in a test tube.
The reason this is a hypocritical crock of shit, is that “due to an abundance of caution”, almost every single “carcinogen” and other “bad boy chemical” that is restricted or controlled in the United States, at the cost of trillions of dollars which go into the pockets of the deep state and China, is because of IN VITRO results.
Thus, if it’s OK to have vaccines that do what Pfizer’s vaccine does, then it’s OK to remove the restrictions on benzene, and have benzene everywhere. Likewise for thousands of other chemicals.
Starting to see how this works? Let’s move on.
Alex Berenson:
Hey, remember how they told you the mRNA in the vaccines could NEVER wind up in human DNA? A new study out of Sweden suggests otherwise (at least in lab-grown cells).
Don’t worry, everything is fine.
After all, we have all that long-term placebo-controlled clinical trial data proving the safety of these mRNA shots.*
So About Not Needing Actual Study…[Comments enabled]
Oh, mRNA won’t get taken up into cell lines and thus can’t propagate on a permanent basis in the human body, we were told.
Indeed that’s rather important. Mutagenic (cancer), cytotoxic (you’re ****ed) and teratogenic (any child you give birth to or sire is ****ed) things that get into cellular DNA can lead to irreversible damage because most cells in the body are replaced on regular basis.
There’s an infamous quote that is in fact wrong: Our body fully replaces itself every seven years. That’s not true. It came out of a study that looked at the average age of cells in a human, using Carbon-14 dating. Anyone who has done any sort of statistical work knows the problem with averages: They are just that, and the statistical outliers are there but unaccounted for with such simplistic tripe.
There are several types of cells that are never replaced. Certain ones in the cerebellum, for example, that deal with coordination and balance, those in the ocular lenses and the eggs in a woman’s ovaries.
There are also cells that are much more-frequently replaced. Red blood cells, for example, have a roughly 90 day life cycle. This is why an A1c test, which measures glycated hemoglobin (that is, red cells that have been damaged by glucose) will tell you what your average blood glucose level has been over the last three months. The epithelial cells in your intestines last only about five days, and the live (dermal) part of your skin is replaced in about 2 weeks. Skeletal muscle and the rest of your intestines, on the other hand, are good for around 15 years.
But with few exceptions it is indeed true that most cells are in fact replaced. This is why you can get cancer; when there is an error in that replication the result can be a cell that has wildly damaged regulatory mechanisms on self-replication. If that damage kills the cell immediately then there’s no real foul, but if it leads to much more rapid reproduction…… that’s cancer.
We have known for quite a while that viruses can and do in some cases infiltrate into DNA. We know this because we’ve found pieces of viral RNA in our genome and not a few of them either; they’re literally all over the human genomic code. It’s wildly improbable that said congruence happened by random alignment of the various codons in our genetic code; ergo, it got in there at some point in evolution and then got into either the eggs of a developing female fetus or the sperm of a male and thus propagated. We only know, of course, about the integrations that weren’t fatal to offspring or the person in question. We also know that in general genetic mutation is harmful or fatal nearly all the time, so that we have said evidence in our genome means this sort of thing happens quite frequently and most of the time it screws the person who has it happen to them.
Indeed some cancers are blamed on viral infections where the viral RNA gets transcribed into the DNA of the cells and causes said errors.
mRNA is not really “new” technology; Moderna has been trying to make it work for cancer, for example, for a long time — without success. The reason for failure has always been dose-related toxicity that has overtaken the benefit when used in sufficient quantity to actually deliver a therapeutic effect. This is not an uncommon reason for drug and therapy failure; in fact that too happens all the time.
But we didn’t bother doing intermediate and longer-term study on the specifics of using mRNA (or, for that matter, a modified virus as with J&J) to deliver a partial viral payload in this regard before rolling it out. Instead, we just trusted that there’d be no integration. Indeed zero epigenic, mutagenic and teratogenic studies were done;they take years to do and we just flat-out didn’t bother. Where we had original control groups in the summer and fall of 2020 we intentionally destroyed them by giving the placebo arm of the original trials the drug three months later, making analysis on any sort of clean analytical basis impossible.
This was wild arrogance given that we know viruses do indeed integrate via infection. To presume it won’t happen here, when we cause cells to produce viral proteins, when the very same thing, producing viruses when a cell is infected, sometimes does is ridiculously and wildly-irresponsible arrogance.
In the BNT162b2 toxicity report, no genotoxicity nor carcinogenicity studies have been provided [26]. Our study shows that BNT162b2 can be reverse transcribed to DNA in liver cell line Huh7, and this may give rise to the concern if BNT162b2-derived DNA may be integrated into the host genome and affect the integrity of genomic DNA, which may potentially mediate genotoxic side effects. At this stage, we do not know if DNA reverse transcribed from BNT162b2 is integrated into the cell genome.
This study does not prove that said genetic pollution has occurred, but it raises the distinct possibility as the precursor events required for this to occur are now known to happen with scientific certainty.
We don’t know because we deliberately did not look; the studies were not done prior to use.
Genomic deoxyribonucleic acid (abbreviated as gDNA[1]) is chromosomal DNA, in contrast to extra-chromosomal DNAs like plasmids. Most organisms have the same genomic DNA in every cell; however, only certain genes are active in each cell to allow for cell function and differentiation within the body.[2]
The genome of an organism (encoded by the genomic DNA) is the (biological) information of heredity which is passed from one generation of organism to the next. That genome is transcribed to produce various RNAs, which are necessary for the function of the organism. Precursor mRNA (pre-mRNA) is transcribed by RNA polymerase II in the nucleus. pre-mRNA is then processed by splicing to remove introns, leaving the exons in the mature messenger RNA (mRNA). Additional processing includes the addition of a 5′ cap and a poly(A) tail to the pre-mRNA. The mature mRNA may then be transported to the cytosol and translated by the ribosome into a protein. Other types of RNA include ribosomal RNA (rRNA) and transfer RNA (tRNA). These types are transcribed by RNA polymerase II and RNA polymerase III, respectively, and are essential for protein synthesis. However 5s rRNA is the only rRNA which is transcribed by RNA Polymerase III.[3]
Used in a sentence:
While we tend to be more concerned about changes to genomic DNA, changes to any kind of human DNA are potentially problematic.
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.
Otherwise Best Described as a Somewhat Strange but Beautiful and Heartfelt Message to the Staff of this Esteemed Company from the People in Logistics on Christmas Eve ON TIME AND UNDER BUDGET – THE TRUMP WAY First of all, Merry Christmas! (And belated Happy Hanukkah if I missed you back then!) Which is actually what …
…..which is a bit of a Ghost of Christmas Past…..
…..kinda like some other treasured site images…..
…..it brought back a lot of fond memories of the early site – a little over 3 years ago…..
…..and so I just wanted to say…..
(1) Merry Christmas, everybody,
(2) Happy Logistics, all you Truckers, Supply Chain Folks, and fellow working humans,
(3) And maybe Happy Logistics to you other working creatures, too. Winged or otherwise!
…..wherever you may be now!
And now, the rules of THIS PARTICULAR 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
This week’s shipment is allegedly CUBISM – to prove that we will put ANYTHING on the wall – even genres we generally don’t like much.
Cubism and Christmas. A good idea? Or NOT A GOOD IDEA? You decide!
OK – let’s get more traditional!
And maybe even VERY traditional!
And speaking of music…..
What’s Playing on the Jukebox
Why, the soundtracks of the trailers in the next section! That’s what!
Here is the trailer song separated from the cinema. I actually find it a bit more enjoyable this way.
Movie Review: Death on the Nile (2022)
NOTE: This review may contain very mild “spoilers”. Stop reading if you run into something that seems spoilerish, if you don’t want any. I have tried to not give away anything significant in the story, beyond the trailers, but there may be a couple of close calls.
This is the movie that I’ll be talking about. This is the trailer you most likely saw.
However, if you got an early preview of it, you may have seen THIS early preview trailer, which has almost no dialog, but is really intriguing by relying only on visuals and music.
Here is yet another version with rearranged visuals – shorter and snappier. I like this one!
There is an IMDB trailer that’s very nice, too, but you have to go there to see it.
Lastly, let me show you a “reaction mashup” – basically looks like a Zoom room – of a bunch of people commenting on the trailer as it plays.
OK – that’s enough. Now down to business.
I have not been to a movie in a while. I really avoid them if I can. I can spot the dirty hands of cultural Marxism in almost every movie Hollywood makes now. It’s tedious to watch their propaganda.
However, my wife likes these damned murder mysteries. Sherlock Holmes, Agatha Christie – you know the type.
The last one we saw was the horrifying “Knives Out” – enjoyable as a work of the genre, but excruciating in its political correctness. The vengeful, angry, projecting, communist psychology was all over it, ramping up to laughable levels at the end. Overtly racist, sexist, classist, and every other leftist prejudice-in-the-name-of-stomping-out-prejudice, all of the hard left’s biases were gleefully woven into both plot and acting. I was rolling my eyes, chuckling, and smirking at the “dramatic” parts at the end. I honestly felt sorry for the “woman of color heroine” at the ideologically “uplifting” end.
Why must the solution to all human idiocy be “deuce axe machinist” by liberals? So they get to be GODS? Using a hammer and sickle on every microscopic problem?
Ugh.
I thought I was done with Hollywood’s corrupting of the “murder mystery” genre, but no – my DW had different ideas.
This one – Death on the Nile (2022) – succeeds mostly by DISTRACTING from the political correctness. It does so with a combination of compelling plotting, amazing scenery, skillful acting, and strong attempts to “go beyond” blatant leftist narratives by underplaying them competently yet powerfully into the story itself. This approach allows the leftist audience to see what THEY want to see, while trading “in-your-face” PC for a kind of non-gratuitous, historically correct PC that makes sense as part of the story.
Still, the PC is not removed completely, and on long reflection, one feels abused by the requisite embedding of political correctness.
For example, while every one of these “usual suspects” is woven skillfully into the plot, they’re still all there:
interracial romance in the face of 1930’s history
“probably racist” white parent forbidding true love
old black woman sage
young black woman muse
bad male gun, bad white gun, good black female gun
wicked white waspy couple (and they’re cultural appropriators, too!)
lesbians forced into the closet by paternalistic society
aspirational capitalist bourgeoisie without morality, tsk, tsk
limousine communist donor class heroine
classic white male hero submits to struggle session and self-criticism
imperialist “woman of color” in denial of roots pays for her transgression
Christian symbols hypocritical, non-Christian symbols meritorious
decadent cabaret culture showcased yet subjected to moral apology RE appropriation
many smaller bits of reflex Hollywood-think
Now – with all that said – these things were made almost completely non-gratuitous by a kind of honest incorporation into the plot, albeit without historically accurate dialog, and RARELY addressing them directly. This leaves an intriguing blend of truth – historical and emotional – in the wrong language, suitable for the modern ear. Actually, Hollywood does this almost ALWAYS, but because I now avoid their work product for months to years at a time, it’s painfully apparent to me.
Thus, the movie creates a skillful blend of political tensions with the NORMAL tensions of a murder mystery. This is a great trick – a kind of cross-talk to influence audiences EMOTIONALLY but not overtly.
The didn’t forget the SEX, either. Lots of STEAMY sexually charged scenes, too, but not much skin. As the Daily Mail put it (and this is one of their longer titles):
Full steam ahead for sex, greed and murder: To celebrate the 100th anniversary of Agatha Christie’s first book (and our first glimpse of Poirot), Nicole Lampert goes behind the scenes on Kenneth Branagh’s VERY racy new film version of Death On The Nile
This is skilled propaganda – and in my opinion it is forced on the story by the requirement that the writing get past “The Black List”. This thing ticks off all the requisite boxes on racial and end-wave feminist cultural Marxism. It also passes muster with the Satanist crowd, IMO, by virtue of the Egyptian setting and their “death cult” stuff.
NEVER FORGET WHAT THEY DID – and by that, I mean what they DID TO US.
SPOILER – graphic photo of Las Vegas carnage below the Luxor obelisk, pyramid, and sphinx.
Yup. This production clearly “green-lighted” by the Luciferians in charge.
Now that I’ve gotten the POLITICAL and the CULTURAL and the RELIGIOUS payload stuff out of the way, what about this movie in normal ways? Is it any good?
I think it was really well-done, and that is what elevates the vehicle above the payload.
Let’s start with one of the reasons I was happy to go see the movie.
Russell Brand is not prominent – not as much as I would have liked – but he’s really, really good. He uses his LACK OF LINES to forcefully project a kind of disturbing, anxious, quiet tension and hidden emotion that brings all sorts of suspicion to his character. I won’t tell you where that goes, but it’s good. When he does speak, he does it quite well, and it contributes to the intensely emotional nature of the film. I have much respect for him as an actor now, even though he was clearly playing one of the “butler-level” parts.
This also speaks to extremely competent direction, of course.
Gal Gadot and Armie Hammer are both excellent, carrying that essential combination of “suspicious as hell” and “wouldn’t hurt a fly” which makes for a good whodunit. Hammer is particularly good at the latter. Gadot manages to pull off dozens of wildly different looks throughout the film, which is damn near a fashion piece. Hammer is just stylish. But is he bad? Not gonna spill the beans here!
You might think Gadot would be the hottie of the movie, but if you go by what is gonna make men hot under the collar, that would be the performance by this gal, Emma Mackey.
Both ladies do some scorching dance moves with Armie Hammer, but Mackey’s were enough to raise my blood pressure into the red zone. She’s also quite excellent in her part – the definitely neurotic, probably psychotic, and quite possibly crazy as a bedbug, jilted ex of the guy, and “former” BFF of the girl.
Complicated business.
This gal has “she did it” painted all over her. But did she? No way. Can’t be. But yet…..
Good acting. Dancing. Whatever!
The movie is banned in Kuwait over Gal Gadot’s Israeli military background, but I have to say – if they were looking for other reasons, this movie has plenty.
Speaking of which…..
These ladies provide some mild comic relief – I was unaware that they’re actually a comedy duo – Jennifer Saunders and Dawn French. What’s interesting here is that they mix in some straight-up politics, and actually poke fun at some of the leftist kind. I’m not going to go into much more detail than that.
OK – I will say one thing. The film actually borrows one of Donald Trump’s best one-liners, and re-uses it in a new context. I kid you not. Most people won’t catch it, but those who are deeply familiar with Trump’s 2016 campaign trail will get a nice laugh. It’s good fun.
Annette Bening and Tom Bateman turn in solid performances as the rich old lady and her goofy mama’s-boy son, the latter who seems far too light in the loafers to be falling for……
Sorry. That might be TMI.
Many of the twists of the movie revolve around the above pair. If you do see this movie…..
EYES ON.
NEXT – the accountant.
The Gadot character’s accountant cousin, played by Ali Fazal, is definitely suspicious as hell. Like all accountants, it would seem, he has a “security plan”, and I have to say, I prefer Suspicious Cousin’s over Emma Mackey’s.
Speaking of security, check out that Tiffany necklace on Gal Gadot. It’s part of the plot.
OK – now who are we missing?
Kenneth Branagh as Hercule Poirot
Tom Bateman as Bouc
Annette Bening as Euphemia Bouc
Russell Brand as Dr. Windlesham
Ali Fazal as Andrew Katchadourian
Dawn French as Mrs. Bowers
Gal Gadot as Linnet Ridgeway-Doyle
Armie Hammer as Simon Doyle
Rose Leslie as Louise Bourget
Emma Mackey as Jacqueline de Bellefort
Sophie Okonedo as Salome Otterbourne
Jennifer Saunders as Marie Van Schuyler
Letitia Wright as Rosalie Otterbourne
Ann Turkel as Meredith Wilson
OK – let’s start with the Otterbournes. They’re actually key characters, around which much of the story takes place. There’s the old lady singer / performer, played by Sophie Okonedo…..
…..and then there is her “young kin manager”, played by Letitia Wright.
These two are in the thick of things, and there are many surprises based on their presence. Obviously these two gals are leaned on heavily for the PC messaging, but in spite of it all, they manage to come off as credible, non-cardboard, and interesting characters. In my opinion, if the screenplay would have pulled some of the “crypto-political” dialogue, and replaced it with solid character development, such as making Wright’s character more of a fully developed romantic counterpart to Mackey’s, the whole movie would have benefited.
Fans of “security devices”, shall we say, are gonna love several scenes with these gals, but I won’t spoil the fun.
Speaking of security, always keep your eye on the butler – especially if she has a hankering for BFD (Big Effin’ Diamonds). This is Rose Leslie, who really pulls off the look of a domestic.
Suspicious Cat really thought this broad was GUILTY. Was he right? NOT SAYIN’.
So who’s left on our list? Two names – one of which appears to have been edited out, or is there by mistake. And that leaves ONLY ONE.
Kenneth Branagh. This guy simply can’t be bad. As ALWAYS, he does a great job here, both as an actor and a director, giving some real depth to the character of Hercule Poirot. That’s some of the most redeeming stuff in the movie, so it’s all you’re getting.
OH! And one last, cute point.
Apparently Hollywood had “issues” releasing the movie because of “scandals” that are guaranteed to make your eyes roll.
How ‘Death on the Nile’ became ‘every publicist’s worst nightmare’
Yes. Hollywood was SKEERED because four of the “talent” got into social media trouble.
From the top…..
First. In Hollyweird, it’s OK to *BE* a cannibal, but don’t get caught loudly pretending you’re one – especially after pissing off a string of important women. Armie Hammer (yes, he’s related to the original commie) apparently likes some pretty kinky play sex, and his exes have loose lips. But is he a real cannibal, or just a loud-mouthed drunk and a loser? Your call…..
But WAIT – there ARE things worse than that. Like making a “tone-deaf” and “cringeworthy” “COVID survivor” video based on the John Lennon “Imagine” lyrics, that got tomatoes from hipsters and Branch Covidians.
WARNING!!! MAXIMUM CRINGE!!!
Please, Gal! Always check with your local communist cadres to make sure that speech is appropriate BEFORE you speak!
But there are things that are even worse than poor correct-think…..
Like WRONG-THINK!
Like retweeting anything mildly skeptical of the COVID vaccine narrative. Or worse still, actually TALKING to vaccine skeptics. OH, NOES!
So yeah. They had to wait until NOW, when apparently the SMOKE CLEARED.
SO – should you go see this movie?
Not my call. Hopefully I’ve told you what you need to know.
Movies are not reality. They’re stories. They’re emotional manipulation. Sometimes they’re political manipulation, too. I’m not actually sure if I’m a better or worse person for having watched this movie. But I felt like I needed to make a RECORD of the experience. Hopefully that record can be put to good use by others.
If you do go, ENJOY THE SHOW. I think you might.
The Andromeda Shot
Thanks to barkerjim, Gail Combs, and Chris, who all got me onto the scent with this one.
Let’s start with “The Andromeda Clot”. This story began when a professional embalmer spoke out on behalf of his profession, stating that once the jabs started, he and other embalmers started seeing long, white, fibrous clots – stringy like plastic – in the veins of deceased victims of heart attacks and strokes.
The story just gets bigger and more shocking from there, as Steve dug in.
Steve interviews a very talkative and inquisitive lady embalmer, speaking on behalf of herself and two embalmer friends. These three embalmers have all seen the clots, and ALL of them independently came to hypothesize that these clots are caused by the COVID vaccines.
If you don’t have time for the video (it’s over an hour), you can read this post by Steve for the highlights.
This interview is FILLED with excellent information about the clots, including this lady’s opinion that (1) there is no way these clots are from post-mortem coagulation, and (2) that the clots seem more prominent in the elderly, and may be exacerbated by immobility and stasis.
Some of the blockbuster “hidden gems” in this interview are “scoops” about what doctors are doing behind the scenes. One is use of ivermectin “on the down low” at the local hospital, which is in a very conservative area. Another is that doctors who are encountering clots in clinical practice, are asking about vaccination status as a possible cause of the clots.
You can’t stop the signal, because the signal is TRUTH.
In my opinion, these clots are so damning, it is MONSTROUS that science is not talking about this phenomenon yet.
Is medicine really that derelict in its duty, that UNDERTAKERS are now the source of SCIENCE?
In my opinion, the media in support of WEF leaders and WEF narratives is how we got here.
Adam Schiff, Joe Biden, Barack Obama, and their ILK are why America is looking a lot like the Soviet Union lately, following close behind Canada, Australia, and New Zealand.
Psaki says the White House has been flagging "problematic posts" on Facebook they believe are misinformation about Wuhan coronavirus. Reminder: Fauci worked with Facebook to ban the lab leak theory, which is factual, for more than a year.
Cuppa Covfefe had the same reaction as I did – that this sounds like the disease in Michael Crichton’s fictional book “Andromeda Strain“, the virus of which turned people’s blood into a rubbery powder.
Gail was thinking that this white fibrous stuff sounds like fibrin, and indeed, there is evidence that spike protein binds to fibrinogen, leading to the inappropriate formation of fibrin.
Here are some references about dysfunctional coagulation from both COVID-19 and spike protein, including vaccines.
I can go on and on, finding papers which demonstrate coagulopathy due to either COVID-19 or the spike protein, but almost nobody in the science world DARES to link any of it to the spike protein vaccines, despite the obvious morbidity, mortality, and pathology of vaccinees – something which is apparent to all intellectually honest people.
For example, the first study cited above is featured in this explanatory blog post:
A vicious circle. Coagulation is not merely a result of inflammation, it causes inflammation also, a process driven by the presence of the spike protein alone and its peculiar interaction with fibrinogen and fibrin.
Now here’s the kicker. If the SARS-CoV-2 virus with its uniquely pathogenic spike protein is a bioweapon, then so also must be the ‘vaccines’, which cause the cells in our bodies to manufacture SARS-CoV-2 spike proteins in their trillions, and it has been demonstrated conclusively that these spikes find their way into the vascular system and circulate to every organ in the body, even the brain. Go figure, as they say.
That last paragraph is not hyperbole. In contradiction to all the toadie journalist “fact-checkers”, REAL SCIENTISTS who have dared to point toward the obvious spike protein culprit have now had their suspicions confirmed.
“Read that again: Protein production of spike is higher than those of severely ill COVID-19 patients!“
And to quote the paper he’s talking about:
We find that BNT162b2 vaccination produces IgG responses to spike and RBD at concentrations as high as those of severely ill COVID-19 patients and follows a similar time course.
This is not hard. Think about it.
disease produces spike protein mostly in respiratory tract and lungs
severely ill COVID-19 cases produce more spike, more disseminated
Pfizer vaccine produces same amount of spike as severe disease
but vaccine produces spike in highly vascularized muscle tissue
patients are encouraged to move deltoid muscle to increase perfusion
Pfizer data (Japan) proves vaccine disseminates throughout body
data proves long half-life of vaccine before release of pseudo-mRNA
other studies show vaccine migrates to lymph nodes
spike-producing pseudo-mRNA likely has unnaturally long lifetime
spike is produced for 60+ days in lymph nodes
vaccine moves through circulatory system via lipid nanoparticles
spike moves from lymph nodes through circulatory system via exosomes
exosomes both contain spike and express it on surface
exposed spike binds to fibrinogen and initiates fibrin formation and clotting
circulatory vaccine spike should cause MORE clotting than does disease
It is NO WONDER that the vaccine earned the nickname “clot shot”.
My bottom line is this:
We cannot stand by while these MONSTERS abort living children slowly with these vaccines.
Remember the wife of familial eugenicist Bill Gates JUNIOR?
It’s very useful to understand BILL GATES SENIOR to get a better feel for the whole clan. The man was not just a eugenicist, but a FABIAN as well.
The other side is getting very desperate to “commit population reduction”, and to do it “by any means necessary”. And to do it – as we have seen – the SNEAKIER, the better.
In my opinion, we have to get LOUD in voice and EFFECTIVE in practice, in spreading the word about the HORROR of the Andromeda shot.
Forcing kids to take these injections is horrifying.
ACT ACCORDINGLY.
We have to support the truckers. We have to end the mandates. We have to end this insane regime.
I believe that making the Bidenistas and Bidenazis EAT THE CLOT SHOT is an important part of how to do that.
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.
Get your rest, Trumpy Bear! You’re going back to the White House!!!
We need to restore sanity in the White House, and it’s time to get Winnie the Pooh OUT.
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 it doesn’t matter, because with God, every day is glorious!
And if you need that in a song…… ONE MORE TIME…..
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.
Thus we are assembled here to peacefully address our grievances to whom they may concern, even each other, using both our freedom of speech and of press, as well as our freedom of religion.
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.
Republican presidential nominee Donald Trump prays with pastors during a campaign visit to the International Church of Las Vegas and the International Christian Academy in Las Vegas, Nevada, U.S., October 5, 2016. REUTERS/Mike Segar
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.
YouTube is absolutely bombarding me with videos of that Japanese art-pop girl-band “Perfume” that I showed on Friday. The YouTube Wocommie Mensheviks must have some foul intention, so I think I’ll go looking for something else, but just ONE video is a good lead-in, so here you go.
Thankfully, YouTube isn’t just recommending girl groups to me, as long as I get OFF a girl group video page, in which case girl groups are THE ONLY THINGS they recommend.
On a “blank” YouTube page, I also get “epic music” now!
This is a nice one. Don’t mind the “furries” and assorted anime characters.
https://youtu.be/XrisCsNzOlo
This is a long one, too – you can come back for it while reading the features below.
Next, we have one of Wheatie’s favorite artists – Two Steps From Hell – celebrating our lady warriors!
Yes – beware those who would go after our kids…….
They might not be expecting WHO exactly it is, who will DELIVER THE MILLSTONES.
So let’s close out with a REAL girl group – complete with a fiddle!
Now THAT’S what I’m talkin’ about!
Call To Battle
Our beloved country is under Occupation by hostile forces.
Daily outrage and epic phuckery abound.
We can give in to despair…or we can be defiant and fight back in any way that we can.
Joe Biden didn’t win.
And we will keep saying Joe Biden didn’t win until we get His Fraudulency out of our White House.
BUT FIRST, let me freshen you up with where things were as of February 3, when Robert Malone had THIS to say about the military data showing that the mandated mRNA jabs were definitively causing harm.
That’s just a quick overview of the problem. Here’s the latest, and in more detail. H/T TradeBait2 for this one. This addresses the jaw-dropping and eye-rolling defense by NIH and their Pentagram buddies, which just dropped military credibility by another factor of two.
Is woke mil causing damage? COMMUNISM always causes damage!
As Malone points out in the latter article, in a beautifully understated way, the “defenders of the jab” are now offering excuses that strain credibility to the breaking point. It is very easy to see that the other side is committed to any deception, of other or of self, to keep the jab train rolling.
They are NOT willing to honestly look at the striking relative dangers of these BAD VACCINES.
Something is very wrong, we can plainly see, but let’s just play along and pretend that this whole ridiculous scenario still deserves debate.
We have plenty of observations at this point, but the “old theory of harmless jabs” is able to play “what about” and temporarily evade many if not most of those explanations, lacking an obviously more compelling theory of WHY THE JABS CAUSE HARM, which would make “whataboutisms” unpalatable, even to those who want to believe them.
Well, is there such a compelling theory?
We have advanced certain key principles which explain things, and those are important.
We know about the pathogenic spike protein.
We know about vaccine migration and persistence.
But something is different, now.
NOW we have a theory which includes both of those things, PLUS a principle of IMMUNOLOGICAL ERROR.
In my opinion, we’re there.
The title of this work is:
Innate Immune Suppression by SARS-CoV-2 mRNA Vaccinations: The role of G-quadruplexes, exosomes and microRNAs
The abstract is instructive, and if you want to “TL;DR” past the rest of things, at least give that a read. Better yet, stick around for my interpretation of the abstract.
ABSTRACT
The mRNA SARS-CoV-2 vaccines were brought to market in response to the widely perceived public health crises of Covid-19. The utilization of mRNA vaccines in the context of infectious disease had no precedent, but desperate times seemed to call for desperate measures. The mRNA vaccines utilize genetically modified mRNA encoding spike proteins. These alterations hide the mRNA from cellular defenses, promote a longer biological half-life for the proteins, and provoke higher overall spike protein production. However, both experimental and observational evidence reveals a very different immune response to the vaccines compared to the response to infection with SARS-CoV-2. As we will show, the genetic modifications introduced by the vaccine are likely the source of these differential responses. In this paper, we present the evidence that vaccination, unlike natural infection, induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. We explain the mechanism by which immune cells release into the circulation large quantities of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance. These disturbances are shown to have a potentially direct causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell’s palsy, liver disease, impaired adaptive immunity, increased tumorigenesis, and DNA damage. We show evidence from adverse event reports in the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines excludes them as positive contributors to public health, even in the context of the Covid-19 pandemic.
What I absolutely LOVE, LOVE, LOVE about this abstract, is that it takes some of the most key points of what the Fake News calls “conspiracy theories” and restates them in fact-bolstered scientific jargon that absolutely cannot be disputed. It’s just beautiful.
Because this abstract is important for understanding as we go into the paper, I’m going to take it “line by line” and explain, so that when we get to the paper itself, you can understand what is being talked about and get the gist of it, even if the scientific nuances are not entirely clear to you.
There are TWELVE sentences, each worthy of consideration.
HANG ON FOR A QUICK WARM-UP RIDE.
Analyzing the Abstract
(1) The mRNA SARS-CoV-2 vaccines were brought to market in response to the widely perceived public health crises of Covid-19.
“Widely perceived”.
This is an unarguable fact. It’s a great way to start the argument. State a truth without leaning on the “real crisis” narrative cheese in the center of the trap.
It does NOT say that the mRNA vaccines were brought to market unreasonably, which is open to debate, and which will be a contested question. Remember – many people (including me) HOPED that new technologies – which we were led to believe were needed – would free us from the virus.
Are you starting to see how they USED Trump? In my opinion, we still don’t understand the full extent of the deception and counter-deception. But none of that is said here – it is just ALLOWED under the statement of fact without narrative.
(2) The utilization of mRNA vaccines in the context of infectious disease had no precedent, but desperate times seemed to call for desperate measures.
“Seemed to”.
This is also factual, if we’re honest. The Jab Justifiers will quibble about veterinary vaccines, and experimental vaccines, and all that, as precedents, but those are quibbles. The truth is, you and I never got one of these genetic vaccines before, and that’s because they had never been approved before.
The beauty of this phrasing – “but desperate times seemed to call for desperate measures” – is that it forces us to admit the context of the phony crisis created by the Fake News and Democrats, by only saying “seemed to call for” instead of “called for”.
What the authors are doing here is dropping out the “fake normal” created by the media.
And THAT is an ongoing lesson for science itself to return to control by science and TRUTH.
This is absolutely true, and absolutely key. The mRNA of the vaccines encodes a FULL “half” of a very particular version of the SARS-CoV-2 spike protein. However, in order to accomplish several goals, the mRNA which WOULD code for that half of the spike protein is substantially altered in several different ways to make the whole process work.
And that leads to the next sentence.
(4) These alterations hide the mRNA from cellular defenses, promote a longer biological half-life for the proteins, and provoke higher overall spike protein production.
There is a lot of nuance here, so I will take some time to explain the 3 items.
(a) These alterations hide the mRNA from cellular defenses
There are multiple reasons that the “mRNA” of the vaccines is not actually normal mRNA, but a kind of “pseudo” mRNA.
Cells have to be careful not to “execute the instructions” of what is essentially WRONG RNA. Cells are a lot like soldiers who have been trained to NOT carry out unconstitutional orders.
The fact that mRNA vaccines and related forms of mRNA-based gene therapy actually work AROUND cellular defenses is a hint RIGHT THERE that they might do something bad. Our bodies are designed to FIGHT OFF foreign mRNA.
Be careful how you interpret what I’m saying there. It’s not an indictment of the mRNA method per se, because MANY if not ALL drugs have to “work around cellular and bodily defenses”. That is a huge part of the science of drug delivery.
HOWEVER, it is always cautionary to admit THAT one is working around defenses, because this will inform one as to the RISKS which are being taken BY working around those defenses.
What if you aren’t actually working around the risks?
So, one truth is that the mRNA has certain bases changed to avoid “tipping off” those defenses. It’s a SNEAKY and LUCKY break that we actually CAN work around those defenses.
But are we doing so CLEANLY and to good outcome?
(b) promote a longer biological half-life for the proteins
This is a HUGE double-edged sword.
Remember – the SARS-CoV-2 spike protein CHANGES SHAPE as it breaks into the cell. When it’s all done, it looks like a different protein – even to antibodies.
The drug designers have (literally, but synthetically) mutated the original reported Wuhan spike protein sequence. The primary reason to do this, is to make the protein “LOCK IN” the original, highly infectious, three-dimensional shape of the “fresh” protein, so that antibodies will form PROPERLY against that, instead of forming against depleted, spent, “used” spike protein. This reduces the chances of ADE (antibody-dependent disease enhancement), which comes from “inappropriate antibodies” that evolved to the WRONG TARGET.
The problem with stabilizing the highly pathogenic spike protein for triggering more desirable antibody formation, is that it also stabilizes the highly pathogenic spike protein for pathogenesis, too.
“WHOOPS!”
So – spike-protein-based “long haul” symptoms from the vaccine can be very long – even compared to long haul from the disease. The synthetic spike protein is really good at sticking around in its mutated, long-lasting, highly pathogenic form.
And THAT might not be a good thing.
Ask this question – why doesn’t the VIRUS do that? Maybe a more stable protein is not only bad for the virus, but also bad for the host, and THAT is in turn bad for the virus AGAIN.
(c) provoke higher overall spike protein production
This is a DIRECT call-out of a problem that will almost certainly lead to arguments with “peer reviewers” who want to defend the vaccines. Note that the wording very intentionally does not say “These alterations are intended to…..[three things]” – it simply says “These alterations….. [three things].”
The alterations are INTENDED to provoke higher overall spike protein antibody production. But the fact is, unless the increase in antibodies comes from better and stronger adjuvants, which act as immunity multipliers, then it’s coming from higher (or otherwise more antigenic and pathogenic) overall spike protein production.
Thus, peer reviewers who want to cover up spike protein malfeasance will likely insist on dragging the wording back to being about the antibodies. This follows the lead of Tony Fauci and his “antibody hypnosis” act, designed to keep attention OFF all of the things that are WRONG with the vaccines.
As you can see, we’re only 4 sentences in, and there is a lot of “battle prep” already going on.
(5) However, both experimental and observational evidence reveals a very different immune response to the vaccines compared to the response to infection with SARS-CoV-2.
This is a very general but very powerful FACTUAL statement, which DEFIES the Fauci / Fake News narrative – a narrative which can’t even bring itself to ADMIT that disease-conferred immunity is a reality.
This is a point about which – if you have read even SOME of the COVID-19 scientific literature – there is literally no debate. Only in the Fake News media and on controlled social media is this twisted. Scientists now marvel ALL THE TIME at the differences between vaccine-conferred immunity and disease-conferred immunity.
And, almost ALWAYS, practically speaking (but ignoring any risks of acquiring immunity), disease-conferred immunity is superior.
You will note that Fauci NEVER talks about this stuff.
But there is more – much more. ANY adverse effects which happen due to the vaccines and not the disease, or happen MORE with the vaccines, rightly count as differences.
The paper is not saying this out loud – but you can understand that it is implied.
This right here – the point about a difference between vaccine immunity and disease immunity – is the HAMMER of the gun going back and making a “clicking” noise.
(6) As we will show, the genetic modifications introduced by the vaccine are likely the source of these differential responses.
THIS HERE IS THE BIGGIE.
There are SO MANY potential implications here, I don’t want to steal their thunder from the analysis of the paper.
However, without knowing ANYTHING FURTHER, this is a profoundly common-sense scientific statement. It is simply saying that different molecules from the virus RNA may lead to different outcomes. That’s almost a no-brainer.
This could happen in multiple different ways.
differences in how the “changed mRNA” is handled by the body
differences in how it is interpreted
differences in the protein product
All of this makes wonderful sense.
(7) In this paper, we present the evidence that vaccination, unlike natural infection, induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health.
Oh, wait – THIS is the biggie.
This is saying that there is an important cellular communication screw-up with mRNA vaccination – a screw-up which does not occur with natural infection. Stated in reverse, there IS an important cellular communication channel opened during natural infection, which is MISSED by the mRNA vaccines.
IN OTHER WORDS, A PROGRAMMING ERROR.
This is all too believable to me, because I’ve seen this before. And NOT just when I “learned to code”.
This is LITERALLY a sibling programming error of what happens when too many vaccines are given at the same time, and interferon signals STEP ON EACH OTHER.
Now the Fake News media “fact checkers” absolutely will not admit that there is a problem with multiple simultaneous vaccines, but once the standard mechanism of vaccine-acquired immunity was explained to me, it became OBVIOUS AS HELL that signal interference was behind the observed but somewhat unpredictable problems with tight vaccine schedules.
You are allowed to have a different scientific opinion from these biased and forked-tongued “fact checkers” with agenda.
But let’s save the details for later.
For now, just remember that humans are evolutionarily adapted for disease, not hacky pseudo-mRNA vaccines. Our PROGRAMMING MODEL – our DESIGN – our API – is different from what the hackers thought they could get away with, and they got caught.
(8) We explain the mechanism by which immune cells release into the circulation large quantities of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites.
More specifics.
This is fascinating, because AND LOGIC is now telling me that it’s not just the vaccine migrating, but spike protein as well.
And THAT explains a LOT.
Do you see how everything is tying together nicely around the pathogenic spike protein that is NOT being degraded soon enough or fast enough, like the VIRUS DOES FOR US?
Think about our little human biome friends next time, science. They may have a BETTER PLAN.
(9) We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance.
OK, this is bad stuff. But it’s also bad stuff that is right up the alley of FAKE SCIENCE to now “discover” and get big bucks to study. It’s DETAILS that cannot be dismissed.
This is the GRENADE thrown into the narrative machine gun bunker with half a second left on the fuse.
KABOOM.
This is where every “me too!” funding whore is going to jump on the bandwagon with justification.
(10) These disturbances are shown to have a potentially direct causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell’s palsy, liver disease, impaired adaptive immunity, increased tumorigenesis, and DNA damage.
Oh, wait! Isn’t this the stuff that Robert Malone warned us about?
Isn’t this the stuff that Ryan Cole spotted?
Isn’t this the stuff that FAKE NEWS ignored and “debunked”, but is now appearing in every possible mainstream source of data?
Common sense is going to win here.
INVESTORS had better TAKE NOTE. The landscape is going to change, IMO.
(11) We show evidence from adverse event reports in the VAERS database supporting our hypothesis.
The beauty of VAERS is that it’s flawed, but we know HOW it’s flawed.
Thus, if you see something that can only be MAGNIFIED by correcting for the known flaws, then you have something you can use.
Just stroll past those Fake News fact checkers and Fake Social Media “con-TROLLS” who spew their talking point about “VAERS IS A FLAWED SYSTEM”. SORRY. Not good enough, trolls.
Everything is a flawed system. Knowing the DIRECTION of the flaws is what turns all systems into useful logical tools.
We will use common sense here, long after these people who deny it are OUT OF POWER.
(12) We believe a comprehensive risk/benefit assessment of the mRNA vaccines excludes them as positive contributors to public health, even in the context of the Covid-19 pandemic.
This is where they land when all is said and done.
They’re saying that they believe the risks outweigh the benefits with THESE vaccines.
This does NOT say that vaccination per se is a bad strategy for COVID-19.
It says that mRNA vaccination as it currently exists is not a good strategy for COVID-19.
It doesn’t say that viral vector cDNA, “full” spike protein subunit antigen, or RBD subunit antigen vaccines are doubtful in any way. They may be, but the authors don’t say that (although some of the specifics DO have implications for the other vaccines).
The authors only say that THESE particular, current, mRNA vaccines are “not positive contributors to public health”.
And you can do the math from there.
Can the current mRNA vaccines be fixed?
Good question. This paper is likely a roadmap to any such fixes. But until then…..
Mandating these vaccines is WRONG, if not INSANE.
Analyzing the Paper
Now we get to the meat of the paper.
I am just going to drop my impressions, placing them in context as needed. On some of these, I blab on and on. On others, I just make a short point. I do a lot of quoting where the authors say it nicely. This is very seat-of-the-pants.
Introduction
The FIRST paragraph is a generous summary of the basics of vaccination, FULLY in compliance with the CDC definitions. Please take note of that. There is no quibbling about the mRNA vaccines not being vaccines.
The SECOND paragraph summarizes and exemplifies the presence in the literature of a viewpoint that the mRNA vaccines are very similar to natural immunity. There is a point made that is basically my contention of Fauci’s “antibody hypnosis”, but it is phrased very politiely.
The U.S. Centers for Disease Control and Prevention (CDC) makes the case based upon antibody titers generated by prior infection vs. vaccination, in addition to production of memory B cells, to argue that the immune response to vaccination is analogous to the response to natural infection [4]. It is this similarity in the humoral immune response to vaccination vs natural infection, paired with both trial and observational data demonstrating reduced risk of infection following vaccination, that stands as the justification for the mass vaccination campaign.
The THIRD paragraph is long, but absolutely key.
It is the summary of the guts of the paper.
You will note that the authors are pointing out EXISTING MAINSTREAM SCIENCE which is contradicting the media-trumpeted, but “CDC-silent” narrative that vaccination is superior to “natural immunity”, by pointing out (without saying it bluntly) that it’s not even AS GOOD as disease-conferred immunity, because known “good” responses to the natural antigen are completely missing.
And worse than that, the mRNA vaccines seem to do WRONG THINGS to the immune system as well.
In this paper we explore the scientific literature suggesting that vaccination with an mRNA vaccine initiates a set of biological events that are not only different from that induced by vaccination but are in several ways demonstrably counterproductive to both short- and long-term immune competence and normal cellular function. These vaccinations have now been shown to downregulate critical pathways related to cancer surveillance, infection control, and cellular homeostasis. They introduce into the body highly modified genetic material. A medRxiv preprint has revealed a remarkable difference between the characteristics of the immune response to an infection with SARS-CoV-2 as compared with the immune response to an mRNA vaccine against COVID-19 [5]. Differential gene expression analysis of peripheral dendritic cells revealed a dramatic upregulation of both type I and type II interferons (IFNs) in COVID-19 patients, but not in vaccinees. One remarkable observation they made was that there was an expansion of circulating hematopoietic stem and progenitor cells (HSPCs) in COVID-19 patients, but this expansion was notably absent following vaccination. A striking expansion in circulating plasmablasts observed in COVID-19 patients was also not seen in the vaccinees. All of these observations are consistent with the idea that the vaccines actively suppress type I IFN signaling, as we will discuss below. In this paper we will be focusing extensively, though not exclusively,on vaccination-induced type I IFN suppression and the myriad downstream effects this has on the related signaling cascade.
Again, I point out that this is being pulled out of the “mainstream” literature.
Does this immune suppression that researchers found remind you of anything?
Note that this is on BitChute because YouTube deleted it as “misinformation”.
If you’re thinking “Wow, the media and social media has really screwed up science!”, well, all I can say is “They won’t be able to walk the streets.”
The FOURTH paragraph then begins dropping bombs on the Pfizer clinical trial shenanigans, which basically covered up the placebo group to obfuscate vaccine problems.
The message is roughly “Because Pfizer covered things up by vaccinating their placebo group, as well as other tricks, we were forced to look at VAERS and the scientific literature to find out what the vaccines are doing – AND BOY, DID WE FIND A TON OF PROBLEMS.”
But done much more politely.
The next two paragraphs are a WITHERING ATTACK on the vaccines, simply using the scientific literature. OMG – the spatter on the walls – there are quite a few easy targets that the Fake News Media has been protecting by ignoring, but it’s very hard to “memory hole” the scientific literature to those who can “pay to play”, so the authors just mention a string of scientific findings that Fauci hoped the public would never see.
Thus, the FIFTH paragraph is a summary of VACCINE FAILURE, with references.
The SIXTH paragraph then brings up the wonderful idea that if benefits are as low as we now understand them to be, maybe RISKS need a closer look.
You may want to read the whole introduction, because that is the last easily readable section of the paper for a while.
NOW it gets really technical.
Interferons: An Overview with Attention to Cancer Surveillance
This section is extremely complex and hard to read, even if you’re familiar with most or all of the various biochemical and biological acronyms that are thrown into the melange.
It starts off with a review of what is known about INTERFERONS (IFNs), as well as substances which regulate them, known as INTERFERON REGULATING FACTORS (IRFs).
This is what you need to know:
Type I IFNs play a powerful role in the immune response to multiple stressors. In fact, they have enjoyed clinical therapeutic value as a treatment option for a variety of diseases and conditions, including viral infections, solid tumors, myeloproliferative disorders, hematopoietic neoplasms and autoimmune diseases such as multiple sclerosis [16].
As a group, IFNs play exceedingly complicated and pleiotropic roles that are coordinated and regulated through the activity of the family of IFN regulatory factors, or IRFs [17]. IRF9 is most directly involved in anti-viral as well as anti-tumor immunity and genetic regulation [18-20].
Basically, interferons are critical players in the CLEANUP OF GENETIC BAD GUYS CAUSING TROUBLE. Those genetic bad guys can be EXTERNAL WRONG-GENES (viruses) or they can be ROGUE CELLS (cancer and the like).
This section then summarizes the complex interactions and feedback loops which characterize anything involving interferons, but particularly related to their anti-cancer role. It is made exceedingly clear that improper interferon levels and disruptions of the complex interferon systems are known to lead very directly to clinical appearance of cancers of various kinds.
Near the end, COVID-19 is brought into the mix. A recent Chinese paper is cited, the work having shown interference with IRF signaling by a non-mRNA, inactivated virus, COVID-19 vaccine. The changes are EXPECTED to reduce resistance to cancers, and the mechanisms are discussed in detail. ELEGANTLY, those same mechanisms are found in Alzheimer’s patients, and appear related to development of dementia symptoms that sound remarkably like COVID brain fog.
Finally, a documented case of a rare lymphoma being accelerated by the Pfizer vaccine is described, and a summary statement is given:
Given the universally recognized importance of optimally functioning BRCA1/2 for cancer prevention and given the central role of the TRAIL signal transduction pathway for additional cancer surveillance, the suppression of IRF7 and IRF9 through vaccination and subsequent spike protein production is extremely concerning for long-term cancer control in injected populations.
Considerations in the Design of mRNA Vaccines
This section basically describes the long list of HACKS – many of them very ELEGANT HACKS – that were needed to get all the way from Robert Malone’s initial discovery which enabled mRNA gene therapy, to where mRNA vaccines are today.
The implications of all these hacks for relevant IMMUNOLOGICAL and GENETIC biochemistry, including INTERFERONS and CANCER, are described.
This section SETS UP the long list of concerns which are going to necessarily follow.
Quite a bit of attention is paid to the components of the lipid nanoparticles, their roles, and their potential risks and side-effects.
This section is fairly readable, and if you’re curious about the various hacks, and particularly the purpose and mechanism of the lipid nanoparticles, then you may enjoy reading past the jargon.
GC enrichment and potential G4 (pG4) structures in vaccine mRNAs
This is a difficult section to understand, if you’re not familiar with DNA and RNA “beyond the double helix”. It’s a bit like Morse code. Everybody knows what Morse code is, and maybe how to do an “SOS”, but not many people remember Morse code well enough to compose and send long signals at will, let alone send a telegram. OTOH, if you’re in genetic medicine or biology, you may be familiar with more than just 4 bases and the double helix.
The bottom line is that, among the various hacks that have gone into the mRNA vaccines, some of them are basically “genetic tricks” to increase production of spike protein. The PROBLEM with that, is that the FINAL implications of some of these tricks are not fully known.
Because there is redundancy in the genetic language, and the efficiency of different spellings is not the same (nite vs. night, thru vs. through, etc.), certain things can be re-encoded using the most efficient letters to create MOAR SPIKE PROTEIN. And MOAR is always BETTER. RIIIIIIIIGHT?
Well, it turns out that spellings have implications for how mRNA behaves. How mRNA behaves has implications for things like CANCER.
Going back to the title of this section, “G” and “C” are the efficient bases that are switched to, to make proteins with higher efficiency. The problem THERE is that “G” can do something every interesting – it can bind with itself in a square, to form a quadruple helix called a “G quadruplex”, which is abbreviated G4. See the image above for cross-sections of such a structure, at the point of binding.
There are ways to predict if a G quadruplex will form – these cases are called “pG4” for “potential G quadruplex”.
Midway through the section, this quote:
Summarizing the topic to this point, the enrichment of GC content in vaccine mRNA will inevitably lead to an increase in the pG4 content of the vaccines. This, in turn, will lead to dysregulation of the G4-RNA-protein binding system and a wide range of potential disease-associated cellular pathologies including suppression of innate immunity, neurodegeneration, and malignant transformation [83].
There are further implications. The more mRNA can form these self-shielding quadruplexes, the less that “micro RNAs” – miRNAs – can bind to the mRNA and control the expression. And THAT leads to another cascade of potentially unintended consequences.
The multitude of pG4s in the mRNA of the vaccine would predictably act as decoys, distracting miRNAs from their normal function in regulating human protein expression. The increase in G4 targets due to the vaccine would decrease the availability of miRNAs to target human-expressed G4s for regulation of gene expression. This can result in downregulation of miRNA expression which is implicated in cardiovascular pathology [96], onset of neurodegeneration [97], and/or cancer progression [98].
Type I IFNs and COVID-19
This is a very interesting section on the relationship of interferons to COVID-19. It appears that:
lower levels of interferons lead to more severe COVID-19 outcomes
IFNs can be used for treatment early, but make things worse if given late
interferons seem to prevent infection by COVID-19
this would explain enhanced susceptibility to COVID-19 after vaccination
COVID patients with antibodies against interferons are common in severe cases
Interferons are clearly key, and look to be one of the most significant differences between the disease and the vaccine.
Are the methylation strategies for cellular housekeeping generally omitted by vaccine mRNAs?
This is a rhetorical question about one of the hacks used by the mRNA vaccines.
To put it a bit too simply, the synthetic mRNA is “capped” both to evade detection AND to generate more spike protein, and most likely without regard for downstream unintended consequences, due to the fact that capping is normally supposed to be both a signaling and a regulating mechanism. The “hack” abuses this feature to make more spike protein.
Rather than simply making an accusation, the question is asked, whether the hack accounted for some of the more likely consequences.
E.g., …..
Furthermore, this also means that eIF4E, which is a powerful oncogene regulator and cell proliferation modulator, will sustain its activities by this competition, for an unnaturally prolonged period of time, trying to counterbalance the competition between robustly-capped mRNAs in vaccines and IRES-containing mRNAs[113,65]. This type of condition results in dysregulation of co-transcriptional m6A mRNA modifications and seriously links to molecular progressions of various cancers [114], as well as creating predisposing conditions for subsequent viral infections [113].
My money is on the idea that nobody in the management chain at Pfizer or Moderna gave a flying F, because Fauci and Walensky are all about the antibodies. This is a CLASSIC downstream effect of antibody hypnosis.
Exosomes and MicroRNAs
This is an interesting grab-bag of stuff, and it’s not that hard to follow, for the most part, so you may want to read it.
Exosomes are basically little bubbles of cell that break off and carry crap, a lot like “virus-like particles” or even “lipid nanoparticles”. It turns out that much of the spike protein which is produced in vaccine-infected cells LEAVES THE SCENE inside exosomes, or studded into their surface. This was in fact discovered by a group in India.
Also, under conditions of overwhelming production of spike protein due to SARS-CoV-2 molecular vaccination, it would of course be expected that a significant proportion of over-abundant intra-cellular spikeproteins would also be exported via exosome cargoes [128]. A seminal paper by a research team in India investigated the role of exosomes in the cellular response to internally synthesized SARS-CoV-2 spike protein [50]. They wrote in the abstract:“We propose that SARS-CoV-2 gene product, Spike, is able to modify the host exosomal cargo, which gets transported to distant uninfected tissues and organs and can initiate a catastrophic immune cascade within Central Nervous System (CNS).”
Things get even worse. It turns out that these exosomes also carry micro-RNAs that turn off interferons in the distant places to which they carry the spike protein.
Thus, the available evidence strongly suggests that endogenously produced spike protein creates a different microRNA profile than does natural infection with SARS-CoV-2, and those differences entail a potentially wide range of deleterious effects.
A central point of our analysis below is the important distinction between the impact of vaccination versus natural infection on type I IFN. While vaccination actively suppresses its production, natural infection promotes type I IFN production very early in the disease cycle. Those with preexisting conditions often exhibit impaired type I IFN signaling, which leads to more severe, critical, and even fatal COVID-19. If the impairment induced by the vaccine is maintained as antibody levels wane over time, this could lead to a situation where the vaccine causes a more severe disease expression than would have been the case in the absence of the vaccine.
Another expected consequence of suppressing type I IFN would be reactivation of preexisting, chronic viral infections, as described in the next section.
SO – this would explain “vaccine-induced disease enhancement” – not antibody-dependent (ADE), but rather interferon-dependent (IDE). And in this case, it could be significantly different diseases that are being enhanced, because of the generality of the interferon network.
Speaking of which…..
Reactivation of Varicella-zoster
Fully consistent with the proposed vaccine-induced negative effects on interferon signaling, would be the significant number of cases of shingles appearing post-vaccination with the mRNA vaccines.
There is also a documented case of viral hepatitis flaring up because of the vaccine.
An additional case of viral reactivation is noteworthy as well. It involved an 82-year-old woman who had acquired a hepatitis C viral (HCV) infection in 2007. A strong increase in HCV load occurred a few days after vaccination with an mRNA Pfizer/BioNTech vaccine, along with an appearance of jaundice. She died three weeks after vaccination from liver failure [142].
Personally, I have no desire to get shingles again.
Impaired DNA Repair and Adaptive Immunity
As stated – more examples from the literature.
We have to speed up here. This is a long paper.
Immune Thrombocytopenia
This is your “clot shot” mechanism, explained.
This quote is interesting.
It has been shown that the mRNA vaccines elicit primarily an immunoglobulin G (IgG) immune response, with lesser amounts of IgA induced [155], and even less IgM production [156]. The amount of IgG antibodies produced is comparable to the response seen in severe cases of COVID-19. It is IgG antibodies in complex with heparin that induce HIT. One can hypothesize that IgG complexed with the spike protein and PF4 is the complex that induces VITT in response to mRNA vaccines. It has in fact been shown experimentally that the receptor binding domain (RBD) of the spike protein binds to PF4 [157].
PPAR-α, Sulfatide and Liver Disease
Two paragraphs are worthy of your attention.
As we have already stated, an experiment by Mishra and Banerjea (2021) demonstrated that the spike protein induces the release of exosomes containing microRNAs that specifically interfere with IRF9 synthesis[50]. In this section we will show that one of the consequences of suppression of IRF9 would be reduced synthesis of sulfatide in the liver, mediated by the nuclear receptor peroxisome proliferator-activated receptor α (PPAR-α).
…
Multiple case reports in the research literature describe liver damage following mRNA vaccines [165-167]. A plausible factor leading to these outcomes is the suppression of PPAR-α through downregulation of IRF9,and subsequently decreased sulfatide synthesis in the liver.
As you can see, there is a prediction here, and plenty of room to investigate.
Guillain Barre Syndrome and Other Neurological Conditions
This is worth reading. There is a laundry list of neurological conditions clearly attributed to the vaccine, and a clear mechanism by which they happen.
Bell’s Palsy
A known problem which appeared during the clinical trials of the mRNA vaccines.
Placebo 1, Treatment 7. Do the math.
Myocarditis
Signals and mechanisms are discussed. Particularly compelling is the proposed role of exosomes in carrying the toxic spike to cardiac tissue.
My money is still on migrating vaccine, but AND LOGIC will do for now.
Considerations Regarding the Vaccine Adverse Event Reporting System (VAERS)
The underreporting of the system is discussed, with some doubt about the commonly cited figure of “100X” underreporting, as well as mention of a more sophisticated figure of 31X obtained by Rose.
VAERS Signal for Immune Suppression, Thrombocytopenia and Neurodegeneration
A comparison of the data from COVID vaccines to ALL OTHER VACCINES COMBINED is made, and the results are impressive.
Many different things are listed. It’s worth looking at.
VAERS Signal for Cancer
After detailing the numbers for cancer (nice table), where the mRNA vaccines have HUGE numbers compared to all other vaccines combined, this statement:
This cannot be explained by reference to a disproportionately large number of people receiving an mRNA vaccination in the past year compared to all other vaccinations. The total number of people receiving a non-COVID-19 vaccination is unknown, but over the 31 years history of reports VAERS contains it is unquestionably many orders of magnitude larger than the number receiving an mRNA vaccination in the past year. Overall, in the above table, twice as many cancer reports to VAERS are related to a COVID-19 vaccination compared to those related to all other vaccines. That, in our opinion, constitutes a signal in urgent need of investigation.
To me, this is enough to say that the mRNA vaccines are related to cancer. Period.
Discussion
This is worth reading:
There has been an unwavering message about the safety and efficacy of mRNA vaccinations against SARS-CoV-2 from the public health apparatus in the US and around the globe. The efficacy is increasingly in doubt, as shown in a recent letter to the Lancet Regional Health by G¨unter Kampf [215]. Kampf provided data showing that the vaccinated are now as likely as the unvaccinated to spread disease. He concluded:“It appears to be grossly negligent to ignore the vaccinated population as a possible and relevant source of transmission when deciding about public health control measures.”
In this paper we call attention to three very important aspects of the safety profile of these vaccinations. First is the extensively documented subversion of innate immunity, primarily via suppression of IFN-α and its associated signaling cascade. This suppression will have a wide range of consequences, not the least of which include the reactivation of latent viral infections and the reduced ability to effectively combat future infections. Second is the dysregulation of the system for both preventing and detecting genetically driven malignant transformation within cells and the consequent potential for vaccination to promote those transformations. Third, mRNA vaccination potentially disrupts intracellular communication carried out by exosomes, and induces cells taking up spike mRNA to produce high levels of spike-carrying exosomes, with potentially serious inflammatory consequences. Should any of these potentials be fully realized, the impact on billions of people around the world could be enormous and could contribute to both the short-term and long-term disease burden our health care system faces.
Given the current rapidly expanding awareness of the multiple roles of G4s in regulation of mRNA translation and clearance through stress granules, the increase in pG4s due to enrichment of GC content as a consequence of codon optimization has unknown but likely far-reaching consequences. Specific analytical evaluation of the safety of these constructs in vaccines is urgently needed, including mass spectrometry for identification of cryptic expression and immunoprecipitation studies to evaluate the potential for disturbance of or interference with the essential activities of RNA and DNA binding proteins.
This is what I was talking about at the beginning. There is enough here for an enormous amount of productive research on the downside of these vaccines. It’s EASY RESULTS. Maybe not easy grant money, but plenty of easy CLOUT when it’s all over.
This does NOT go back in the toothpaste tube.
Conclusions
Presented in whole:
It is imperative that worldwide administration of the mRNA vaccinations be stopped immediately until further studies are conducted to determine the extent of the potential pathological consequences outlined in this paper. It is not possible for these vaccinations to be considered part of a public health campaign without a detailed analysis of the human impact of the potential collateral damage. It is also imperative that VAERS and other monitoring system be optimized to detect signals related to the health consequences of mRNA vaccination we have outlined. We believe the upgraded VAERS monitoring system described in the Harvard Pilgrim Health Care, Inc. study, but unfortunately not supported by the CDC, would be a valuable start in this regard [208].
In the end, we are not exaggerating to say that billions of lives are at stake. We call on the public health institutions to demonstrate, with evidence, why the issues discussed in this paper are not relevant to public health, or to acknowledge that they are and to act accordingly. Until our public health institutions do what is right in this regard, we encourage all individuals to make their own health care decisions with this information as a contributing factor in those decisions.
That’s where I’m at. Do not take the clot shot. Do not give it to your kids. Tell people how you honestly feel.
I am OK with people having the freedom to take a bad vaccine, but I personally think that coercing anybody in the slightest to take it, is a CRIME.
If you’re scared of getting or giving COVID, there are far better ways to deal with it, than a bad vaccine that does a lot of damage.
Can the mRNA Vaccines Be Fixed?
That’s MY question.
I suspect that they CAN be fixed, but not for at least several years – maybe 5-10, if we’re lucky.
Until then, they should be taken off the market, IMO.
Hopefully antigen vaccines will do better, but if they don’t, we can fall back to treatment and “real” immunity.
Wolfie’s Wheatie’s Word of the Day:
wolven
noun
Of or pertaining to wolves; wolflike; wolfish.
Used in a sentence:
Adjectives for wolf include wolfish, wolfless, wolflike, wolfly, wolfy, wolven, wolvish, wolfed, wolfing, wolved and wolving.
(If you can find a better one, please add it to the comments!)
I have been reminding folks on here – the Fed has to be bankrupted at some point. It will either be by the white hats or the black hats. The Gab post you show is correct for the most part IMO. The Fed has fueled the Great Reset, which is why they could care less about how much debt we have in America because we will not exist as an independent nation in their black hat world.
Digital one world currency is the plan. Why do you think there were coin shortages recently? Why do you think they hate crypto and parallel economies so much? Why do they want America at odds with Russia, but falling right in line with China? Where Xi falls in this I am not certain. But I do know China and the Chi-coms are a CB [central bank] creation.
The linchpin is digital currency.
Follow the money….
That is the first half of the comment
Actually I can see where he is going since I also have warned of this much earlier.
The Push For World Government
A few years ago Soros directed the USA to overthrow the ELECTED government in both Syria and Ukraine. (Trump side stepped both.)
Why? Because the EU is the model for a global government. Soros wanted the EU to annex the Ukraine. The elected president said HE!! NO! so he was ousted and a pro-EU puppet was put in his place who has since been voted out while Trump was in the White House.
Russia tossed Soros out and put out a warrant for him. Russia makes much of their money selling gas to Europe. It also gives them leverage to keep the EU from expanding into their sphere of influence. Soros wants to remove Russia’s leverage by putting in a pipeline from the middle east to Europe. ALL the countries that were opposed to that pipeline have been overthrown EXCEPT for Syria.
If you want a World Government similar to the European Union then you are on Soros side. If you want sovereign nations you are on the side of Russia….. AND I am still of that opinion.
BREXIT THE MOVIE will give you the details on how the EU is actually run.
Former World Trade Organization Director-General Pascal Lamy tells you point blank that the EU is the template for the desired World Government and it has been the plan since the 1930s.
All had lived through the chaos of the 1930s — when turning inwards led to economic depression, nationalism and war. All, including the defeated powers, agreed that the road to peace lay with building a new international order — and an approach to international relations that questioned the Westphalian, sacrosanct principle of sovereignty…
Lamy is quite blunt in stating national sovereignty is passé:
…more than half a century ago that the Frenchman Jean Monnet, one of the shapers of post-war Europe, said, “The sovereign nations of the past can no longer provide a framework for the resolution of our present problems. And the European Community itself is no more than a step towards the organizational forms of tomorrow’s world.” His assessment was as valid then as it is now….
This is what Global Warming was really about. We have all seen the political message morph over the decades from Global Warming to Climate Change to Weather Weirding.
As H.L. Mencken said:
“The whole aim of practical politics is to keep the populace alarmed — and hence clamorous to be led to safety — by menacing it with an endless series of hobgoblins, all of them imaginary.”
“The urge to save humanity is almost always only a false face for the urge to rule it.”
The UN put the concept into practice via the IPCC. The IPCC mandate states:
The Intergovernmental Panel on Climate Change (IPCC) was established by the United Nations Environmental Programme (UNEP) and the World Meteorological Organization (WMO) in 1988 to assess the scientific, technical and socio-economic information relevant for the understanding of human induced climate change, its potential impacts and options for mitigation and adaptation. http//www.ipcc-wg2.gov/ (No longer available)
IPCC
Notice the IPCC ASSUMES the hypothesis of human induced climate change IS TRUE and goes from there.
With Reagan killing off the Cold War, Pascal Lamy takes ‘Practical Politics’ the next step, by telling us about a “new enemy to unite us” (Global Warming) A global enemy needed to create Legitimacy, one of the ‘four legs’ needed to implement a global government…
I see four main challenges for global governance today.
The first one is leadership, i.e. the capacity to embody a vision and inspire action, in order to create momentum. Who is the leader? Should it be a superpower? A group of national leaders? Selected by whom? Or should it be an international organization?
The second one is efficiency, i.e. the capacity to mobilize resources, to solve the problems in the international sphere, to bring about concrete and visible results for the benefit of the people. The main challenge here is that the Westphalian order gives a premium to “naysayers” who can block decisions, thereby impeding results. The ensuing viscosity of international decision-making puts into question the efficiency of the international system.
The third one is coherence, for the international system is based on specialization. Each international organization focuses on a limited number of issues. The World Trade Organisation deals with trade, the International Labour Organisation with labour issues, the World Meteorological Organisation with meteorology and so the list continues. It is a fact: the UN is not really overarching, assuming this was the initial intention.
The last challenge that I see is that of legitimacy— for legitimacy is intrinsically linked to proximity, to a sense of “togetherness”. By togetherness, I mean the shared feeling of belonging to a community. This feeling, which is generally strong at the local level, tends to weaken significantly as distance to power systems grows. It finds its roots in common myths, a common history, and a collective cultural heritage. It is no surprise that taxation and redistribution policies remain mostly local!
There is one place where attempts to deal with these challenges have been made and where new forms of governance have been tested for the last 60 years: in Europe. The European construction is the most ambitious experiment in supranational governance ever attempted up to now. It is the story of a desired, delineated and organized interdependence between its Member States…. http://www.wto.org/english/news_e/sppl_e/sppl220_e.htm
Pascal Lamy
In another presentation Lamy again addresses the problem of legitimacy:
By now, with Al Gore exiting stage left, Trump entering stage right, it is pretty obvious that ‘Global Warming’ has lost its high panic factor and the climb down is in progress. However the need for a ‘Crisis to Unite Us’ and a reason to implement ‘Agenda 21 – Sustainability’ and ‘Global Governance’ still remains. WORSE for the Globalists the fiat currency central banking system is on its last legs and about to IMPLODE, as many people like Dave of the X22 Report and Clif High and others have been warning us. Up to now we have been wondering what the next hobgoblin would be. And now we know it’s COVID -19!!! A Bio-Weapon and a Poison Jab that kills off a lot of the population, crashes the world economy and ushers in a Vaccine Digital Passport soon to be linked to the BRAND NEW DIGITAL WORLD CURRENCY and Social Credit Score.
And that brings us to the second part of TradeBait2’s comment.
…… You do not want to use the Nuremberg Code as your get out jail free card from jabs. You fall into the hands of international law superseding national law. It’s a set up, don’t fall for it.
Cannot tell you the number of times I have prepared a post and deleted it because I doubted folks on here would pay attention or believe it. This is the world I lived in for 35 years and escaped.
As I showed above that “international law superseding national law” is exactly what Pascal Lamy was yammering about a decade ago and what Klaus Schwab is threatening us with now.
So how do we escape this TRAP if it is being set?
Use USA LAW!
I find it interesting that the internet is FULL of the Nuremberg Code…….
……and the GERMAN/CALIFORNIA LAWYER Reiner Füllmich and 50 Lawyers, but I went nutz trying to find the US LAWS. It took me over ½ hour.
And WHY does Reiner Füllmich have no problem with YouTube???? When everyone else gets the boot?
I watched it for about half an hour and thought it was important enough to post here. The dozens of witnesses/experts that will be speaking in the next days are from around the world…many of the names you may already know.
Day 1 Opening Session of the Grand Jury Proceeding
A group of international lawyers and a judge are conducting criminal investigation modeled after Grand Jury proceedings in order to present to the public all available evidence of Covid 19 Crimes Against Humanity to date against “leaders, organizers, instigators, and accomplices” who aided, abetted, or actively participated in the formulation and execution of a common plan for a pandemic
I think Reiner Füllmich and his group is sincere but it is very very possible they are being used.
So after a LOT of digging at Cornell Law I found the provision that covers the situation for the military: 10 U.S.C. § 1107.“This provision prohibits the administration of investigational new drugs, or drugs unapproved for their intended use, to service members without their informed consent.”
And finally after a lot more searching I stumbled across the information that civilians are covered under a FDA Regulation and not a law: CFR – Code of Federal Regulations Title 21 as of January 6, 2022
[Code of Federal Regulations] [Title 21, Volume 1] [CITE: 21CFR50.20]
TITLE 21–FOOD AND DRUGS CHAPTER I–FOOD AND DRUG ADMINISTRATION DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER A – GENERAL
PART 50 — PROTECTION OF HUMAN SUBJECTS Subpart B – Informed Consent of Human Subjects Sec. 50.20 General requirements for informed consent. Except as provided in §§ 50.23 and 50.24, no investigator may involve a human being as a subject in research covered by these regulations unless the investigator has obtained the legally effective informed consent of the subject or the subject’s legally authorized representative. An investigator shall seek such consent only under circumstances that provide the prospective subject or the representative sufficient opportunity to consider whether or not to participate and that minimize the possibility of coercion or undue influence. The information that is given to the subject or the representative shall be in language understandable to the subject or the representative. No informed consent, whether oral or written, may include any exculpatory language through which the subject or the representative is made to waive or appear to waive any of the subject’s legal rights, or releases or appears to release the investigator, the sponsor, the institution, or its agents from liability for negligence. [46 FR 8951, Jan. 27, 1981, as amended at 64 FR 10942, Mar. 8, 1999]
BUT there is a cockroach in the ointment.
§ 50.24 – Exception from informed consent requirements for emergency research.
[Code of Federal Regulations] [Title 21, Volume 1] [CITE: 21CFR50.24]
TITLE 21–FOOD AND DRUGS CHAPTER I–FOOD AND DRUG ADMINISTRATION DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER A – GENERAL
PART 50 — PROTECTION OF HUMAN SUBJECTS Subpart B – Informed Consent of Human Subjects Sec. 50.24 Exception from informed consent requirements for emergency research. (a) The IRB responsible for the review, approval, and continuing review of the clinical investigation described in this section may approve that investigation without requiring that informed consent of all research subjects be obtained if the IRB (with the concurrence of a licensed physician who is a member of or consultant to the IRB and who is not otherwise participating in the clinical investigation) finds and documents each of the following: (1) The human subjects are in a life-threatening situation, available treatments are unproven or unsatisfactory, and the collection of valid scientific evidence, which may include evidence obtained through randomized placebo-controlled investigations, is necessary to determine the safety and effectiveness of particular interventions. (2) Obtaining informed consent is not feasible because: (i) The subjects will not be able to give their informed consent as a result of their medical condition; (ii) The intervention under investigation must be administered before consent from the subjects’ legally authorized representatives is feasible; and (iii) There is no reasonable way to identify prospectively the individuals likely to become eligible for participation in the clinical investigation. (3) Participation in the research holds out the prospect of direct benefit to the subjects because: (i) Subjects are facing a life-threatening situation that necessitates intervention; (ii) Appropriate animal and other preclinical studies have been conducted, and the information derived from those studies and related evidence support the potential for the intervention to provide a direct benefit to the individual subjects; and (iii) Risks associated with the investigation are reasonable in relation to what is known about the medical condition of the potential class of subjects, the risks and benefits of standard therapy, if any, and what is known about the risks and benefits of the proposed intervention or activity. (4) The clinical investigation could not practicably be carried out without the waiver. (5) The proposed investigational plan defines the length of the potential therapeutic window based on scientific evidence, and the investigator has committed to attempting to contact a legally authorized representative for each subject within that window of time and, if feasible, to asking the legally authorized representative contacted for consent within that window rather than proceeding without consent. The investigator will summarize efforts made to contact legally authorized representatives and make this information available to the IRB at the time of continuing review. (6) The IRB has reviewed and approved informed consent procedures and an informed consent document consistent with § 50.25. These procedures and the informed consent document are to be used with subjects or their legally authorized representatives in situations where use of such procedures and documents is feasible. The IRB has reviewed and approved procedures and information to be used when providing an opportunity for a family member to object to a subject’s participation in the clinical investigation consistent with paragraph (a)(7)(v) of this section. (7) Additional protections of the rights and welfare of the subjects will be provided, including, at least: (i) Consultation (including, where appropriate, consultation carried out by the IRB) with representatives of the communities in which the clinical investigation will be conducted and from which the subjects will be drawn; (ii) Public disclosure to the communities in which the clinical investigation will be conducted and from which the subjects will be drawn, prior to initiation of the clinical investigation, of plans for the investigation and its risks and expected benefits; (iii) Public disclosure of sufficient information following completion of the clinical investigation to apprise the community and researchers of the study, including the demographic characteristics of the research population, and its results; (iv) Establishment of an independent data monitoring committee to exercise oversight of the clinical investigation; and (v) If obtaining informed consent is not feasible and a legally authorized representative is not reasonably available, the investigator has committed, if feasible, to attempting to contact within the therapeutic window the subject’s family member who is not a legally authorized representative, and asking whether he or she objects to the subject’s participation in the clinical investigation. The investigator will summarize efforts made to contact family members and make this information available to the IRB at the time of continuing review. (b) The IRB is responsible for ensuring that procedures are in place to inform, at the earliest feasible opportunity, each subject, or if the subject remains incapacitated, a legally authorized representative of the subject, or if such a representative is not reasonably available, a family member, of the subject’s inclusion in the clinical investigation, the details of the investigation and other information contained in the informed consent document. The IRB shall also ensure that there is a procedure to inform the subject, or if the subject remains incapacitated, a legally authorized representative of the subject, or if such a representative is not reasonably available, a family member, that he or she may discontinue the subject’s participation at any time without penalty or loss of benefits to which the subject is otherwise entitled. If a legally authorized representative or family member is told about the clinical investigation and the subject’s condition improves, the subject is also to be informed as soon as feasible. If a subject is entered into a clinical investigation with waived consent and the subject dies before a legally authorized representative or family member can be contacted, information about the clinical investigation is to be provided to the subject’s legally authorized representative or family member, if feasible. (c) The IRB determinations required by paragraph (a) of this section and the documentation required by paragraph (e) of this section are to be retained by the IRB for at least 3 years after completion of the clinical investigation, and the records shall be accessible for inspection and copying by FDA in accordance with § 56.115(b) of this chapter. (d) Protocols involving an exception to the informed consent requirement under this section must be performed under a separate investigational new drug application (IND) or investigational device exemption (IDE) that clearly identifies such protocols as protocols that may include subjects who are unable to consent. The submission of those protocols in a separate IND/IDE is required even if an IND for the same drug product or an IDE for the same device already exists. Applications for investigations under this section may not be submitted as amendments under §§ 312.30 or 812.35 of this chapter. (e) If an IRB determines that it cannot approve a clinical investigation because the investigation does not meet the criteria in the exception provided under paragraph (a) of this section or because of other relevant ethical concerns, the IRB must document its findings and provide these findings promptly in writing to the clinical investigator and to the sponsor of the clinical investigation. The sponsor of the clinical investigation must promptly disclose this information to FDA and to the sponsor’s clinical investigators who are participating or are asked to participate in this or a substantially equivalent clinical investigation of the sponsor, and to other IRB’s that have been, or are, asked to review this or a substantially equivalent investigation by that sponsor. [61 FR 51528, Oct. 2, 1996]
And now we go to USA lawyer, Attorney Thomas Renz and his interview on Bannon’s War Room.
Episode 1,619 – Beijing Olympics Fail; Legal/Financial Investigations Of Big Pharma
ATTORNEY THOMAS RENZ:We have to get it to the public and that is where the War room is so important. Se are going to be submitting this to a case in Alabama. We are going to be submitting ths to a number of different places in the military, ahhh I guess law enforcement world. And we are looking to bring this into the civilian law enforcement as well. There is no question as to what is happening. These are major crimes and you know Steve, I don’t know if you have got this but we just yesterday, dated February 4th, got a document from the CDC that re-affirms everything we said last week when we said they know this. If you are interested that document actually says it is was in the meeting yesterday, it was presented yesterday it says the CDC is working to monitor these things and they are monitoring the DOD data. Which indicates to me, I don’t know if you have heard the DOD s response? DOD to me has committed fraud and conspiracy. They have said there baseline data from 2016 to 2020 was wrong. They didn’t notice it until we pointed it out in the whistle blower testimony. But some how even though they didn’t notice it, it magically got corrected in 2021.
I mean seriously, How stupid do they think the American people are?
STEVE BANNON:What about adjudicating this. What about Alabama? (21:40)
RENZ: We have a case in Alabama where we are challenged the EUA authorization of the vaccine….. Balance of harm tests…. Generally you have to show more benefit than injury… we are also challenging on mis branding, because the CDC changed the definition of vaccines so they could call these gene therapies a vaccine. BTW Pfizer and Moderna have admitted they are gene therapy in their documents. And we have challenged it on several other fronts so that’s in court. This document and all this DOD stuff just came to us. We have declarations under penalty of perjury and those declarations will be submitted to the court. They are getting updated right now because we’ve had this new data come forward related to this…. We have been working with attorneys all over the world and around the country… and we have been getting this data out and we are giving it to anyone who wants to use it anywhere they can. And we believe it will help. We have to find the right court like you said. Until we find a court that is willing to listen and have an evidentiary hearing, it’s tough. We are going to have more info on that coming up…..
STEVE: asks about military JAG system and Senator Johnson. Senator Johnson first.
RENZ:The problem for Senator Johnson is he is not getting enough support from other Senators. He has gotten NO RESPONSE from anyone else [including Rand Paul but he does not say that.]
STEVE:What about JAG? [24:50]
RENZ: Since the data has only been out for a week or two, we are working thru a number of JAG officers….. I got another letter this week…. From all places the Texas National Guard, one of the people there saying they are going to reject all the religious exemptions and we don’t want doctors giving medical exemptions. They actually say they view it as a COMMAND ISSUE and not a medical issue. So if a doctor thinks a soldier should not have this for a medical reason, they are to shut-up and take orders according to this document. We submitted that to Senator Johnson as well as some others.
This is a disaster in the military and they have created a situation where it is very very difficult for our solders to fight this. We do however have quite a number of military personnel stepping forward. And quite a number of JAG officers and others who, because of the publicity we have gotten on this, in the last week or so, are now wiling to step up and do something so we’ll see.
A very informative earlier video from the War Room showing the DOD changing the data from Thomas Renz. It also has Ed Dowd, a Financial guru who worked for Blackrock…. Yeah, Blackrock. He is calling out not only the vaccine manufacturers but the FDA for massive FINANCIAL fraud similar to ENRON. The video also has an interview with Dr Malone.
We may serve “off-label” drinks here, including hydroxychloroquine, ivermectin, and truck diesel, but we don’t serve spike protein, remdesivir, or anything made in Wuhan, Chinazia.
While our beloved REAL bartender takes a needed break of unknown duration, we continue to ENDEAVOR TO PERSEVERE.
Christmas Spirit
Feel free to celebrate the birth of Christ any time. We’re dragging it out this year! One MORE month of Christmas begins!
Hey – where’s Santa? We need his famous line about his VP!
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!
#FJB – Free the January Brothers
Current Art On The Wall
This is another off-beat shipment. “Spice” is all it said on the box. Let’s take a look.
I am informed that this one has something to do with the “Spice Islands”.
This one is related to Morocco. I think I see some kind of actually trustworthy pharmaceuticals, although it also looks a bit like that “pot-poury” stuff.
Not sure what this one is, other than what’s on the label – “Moroccan Spice”.
This one is also labeled “Moroccan Spice”, with a reference URL. I am informed by an expert that this genre of art is something known as “purse porn”.
This one is even cheaper. $9.99 at Walmart. Well, it’s FREE here!
Still Life with Spices and Olive Oil Food Still Life Kitchen Photo Print Wall Art By Andrii Gorulko
More in the same genre, but with a nod to local astronomers and others like me who enjoy looking at the sky at night and going WTF.
Baking For Stargazers by Dina Belenko
This is a trick to flush out any kids on this site.
If you ever saw one of these in real life, you’re a kid, or you had some. Or both!
And then somebody decided to get cute with the jukebox…..
On The Jukebox
This is from the early days, when the “talent” was just getting started, and it shows.
Here’s where the “spice” started flowing to the cabal coffers, and the recruits were now famous for being famous. Different fan-exciting material was possible…..
I was going to queue up some of their reunion material, but I absolutely cannot take any more of it.
SO ENJOY.
There – that’s better!
OK, I cannot leave you with that earworm, so I’m going to perform a really neat trick.
The following performance is by a similar “girl group” in Japan, doing a number called “Spice“. Because it’s designed to infect the brains of Japanese and not Westerners, it’s essentially white noise MK to gai-jin, and will erase the Spice Girls stuff.
WE HOPE.
You can turn on English captions to see what they’re saying.
Because this group “Perfume” rides on a more techno/electronica carrier wave, and comes in at a more “artistic” level than the Spice Girls, it actually gets MUCH more respect than the Spice Girls, in both the East and the West. Many people regard it as techno art-pop rather than J-pop. But don’t kid yourself. Down deep, it’s still a “girl band”. These ladies are huge cultural celebrities in Japan, just like the Spice Girls remain in England, even disbanded.
And thus we return to reality.
Or do we?
THE SPICE MUST FLOW
And now for our feature presentation…..
The End of the mRNA Vaccines
This topic right here is just a WARM-UP for my Monday post, which will explain WHY these particular mRNA vaccines are OVER. GONE. KAPUT. DONE.
You want to know why Joe Rogan / Spotify happened?
Pfizer-CNN-DNC-BlackRock-[CB]-Mr.Global can’t attack Drs. Malone and McCullough directly, at this CRITICAL MOMENT, so they FAKED IT, and attacked Joe Rogan to indirectly “prove” that Malone and McCullough are providing “misinformation”.
That is how desperate they are.
Sorry.
As China said to the Biden administration, “You are dealing from a position of weakness.”
The TRUTH is a SOLID FORTRESS.
“They” are in so much trouble.
And Malone and McCullough are in the CATBIRD SEAT.
There are tens of billions – hundreds of billions – maybe trillions of dollars on the line, and those dollars are not just on a rickety foundation – they are on QUICKSAND.
You can understand the panic. And it will only get worse.
First, I want you to watch this video, and understand that every word you hear is 100 times truer than even those people realized when they said those things.
Hat tip to Gail Combs for cluing me in to this very recent paper, which I expect to come under merciless attack, but it won’t do any good.
This paper may NEVER reach or pass “peer review”, but it doesn’t matter. Even if it NEVER passes peer review, the payload has been delivered.
The paper has DETONATED in information space.
More “cautious” scientists will BET THEIR CAREERS on the truth therein, and “discover” everything discussed here, but in slower, politically correct, and damage-controlling ways.
Limited damage control remains possible if “they” are extremely lucky and drop mandates world-wide NOW. But as long as their side keeps forcing mandates, the WOODEN STAKE OF TRUTH will be driven into the VAMPIRE HEARTS OF PFIZER, MODERNA, AND ALL WHO BACKED THE CLOT SHOT.
GOVERNMENTS are going to FALL.
I think that SOMEBODY knew this paper was coming.
Once you see WHY the mRNA vaccines are fundamentally flawed, you can’t unsee it.
Innate Immune Suppression by SARS-CoV-2 mRNA Vaccinations: The role of G-quadruplexes, exosomes and microRNAs
[Could have said “Baylor College of Medicine”, but they were FOOLS!]
ABSTRACT
The mRNA SARS-CoV-2 vaccines were brought to market in response to the widely perceived public health crises of Covid-19. The utilization of mRNA vaccines in the context of infectious disease had no precedent, but desperate times seemed to call for desperate measures. The mRNA vaccines utilize genetically modified mRNA encoding spike proteins. These alterations hide the mRNA from cellular defenses, promote a longer biological half-life for the proteins, and provoke higher overall spike protein production. However, both experimental and observational evidence reveals a very different immune response to the vaccines compared to the response to infection with SARS-CoV-2. As we will show, the genetic modifications introduced by the vaccine are likely the source of these differential responses. In this paper, we present the evidence that vaccination, unlike natural infection, induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. We explain the mechanism by which immune cells release into the circulation large quantities of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance. These disturbances are shown to have a potentially direct causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell’s palsy, liver disease, impaired adaptive immunity, increased tumorigenesis, and DNA damage. We show evidence from adverse event reports in the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines excludes them as positive contributors to public health, even in the context of the Covid-19 pandemic.
I was only part-way through the body of the paper, when I realized that if even a fraction of it is correct, the mRNA vaccines are as good as over.
Worse than that, other non-mRNA vaccines are likely subject to many of the same concerns.
It may very well be that vaccination is a poor strategy for this virus, SARS-CoV-2.
BUT ONE THING IS CERTAIN.
Now that there is a clean, elegant, and intellectually appealing explanation of the adversity of the mRNA clot shot, which happens to align perfectly with common sense, mandates are murder.
Do not back down. Do not give up. We are on the right side of this.
I will explain.
SOON.
Bad Medicine as a Weapon of War
If you ever find yourself weakening on NOT GETTING THE CLOT SHOT – (and I’ve actually run into some of these failure-of-will cases in real life, so it’s not impossible) – try to remember just ONE of the items discussed below.
Don’t let Chinazia and the Globonazis inject you with their Slow-Motion Koolaid designed to assassinate America.
What follows are several items (or groups of items), many of which have been sitting around in my tabs, which have been bothering me. I have been TRYING to fit them into a pure and simple negligence scheme, and I simply can’t.
There is a highly destructive and very intentional aspect to all that has happened, that defies letting us categorize “Obamacare and what came after it” as mere stupidity.
insurance data showing manifold increased deaths of military-aged people, mostly men
Hat tips to RAC, Aubergine and Linda, for bringing the full extent of this one to my attention.
Further hat tips to those who brought all the other “tabbed” items above.
To me, this is only explained by what amounts to a secret “war” against the United States. Not everybody fighting on “their” side knows everything. In fact, almost all of them know nothing. But I think that Tony Fauci, Hillary Clinton, and a few others either know the entirety of the plot, or are following orders without question.
Their mission is based on ideas that America is bad and responsible for every bad thing, and that America and Americans need to be disempowered and punished for it.
Thus, like the general idea that Obama wasn’t as much “for Russia” or “for China” as he was “against America”, we can see that the modern Democrat party is now an embodiment of skepticism about, if not antipathy toward, America and Americans themselves.
Here’s the video and the URL, which long ago disappeared from YouTube.
In my opinion, this all goes back to the Soviet-supported MAOIST Weather Underground types of the late 60s and early 70s, who were actively planning a revolution in which 25 million Americans would need to be killed. This is around the same time that Klaus Schwab got his start. INTERESTINGLY ENOUGH.
There are basically two sides – individual freedom and state control. In the past we’ve tended to have wars which were not cleanly on that boundary, such as Hitler vs. Stalin, but I think THIS ONE is fairly clean. “They” try to make “free forces” fight each other, which is very smart, but I think we’re wising up.
They HAD to have known that, without getting the guns, they could never defeat us ON AMERICAN SOIL.
It HAD to be gradual. It HAD to be Sun Tzu. It HAD to be carried out by Americans, on American soil.
I am really thinking now that SOMEBODY on the radical left realized that they could not set up CAMPS unless we were fully under the grip of socialism, like China or North Korea, BUT that until such a time, there WERE ways to trick us into allowing ourselves to be killed.
Disease used as a weapon of war can be efficient, but it’s obvious. But using the medicine allegedly meant to TREAT a disease as a weapon of war is NOT obvious.
Turning our own medical system against us is a cruel and cynical method of war, but I have to admit that it’s rather brilliant.
It’s a sobering thought.
Something is very wrong here. Stay frosty. I think that they’re trying to get as much as they can WITHOUT WAR, before they actually go TO WAR.
And speaking of WAR……
Mayor Gramsci III’s War On Freedom of Movement
The son of the torch-bearer of Antonin Gramsci, a founding father of cultural Marxism, is not exactly undamaged goods. As you can see above, Pothole Pete was (assuming this bit of news is not completely phony) a PRETTY SICK KID.
People like that are PSYCHOPATHS. Pet murderers rarely turn into saints. There is usually something VERY wrong with them – something that does NOT go away without a lot of GOD in the process.
Personally, I don’t care to push a campaign against “Mayor Pete” over his alleged juvenile criminality. There is a reason that juvenile records are sealed. Many if not most people “get serious” at the point of LEGAL RESPONSIBILITY. They grow up. Bad kids can turn out good. However, I still think Kid Pete’s history is relevant to Secretary Pete’s personality.
We’ve gotta KEEP OUR EYE on this boy.
I suspect that many people are glad “Possible Pet-Killer Pete” is “only” Secretary of Transportation. Still, he could do a LOT of damage there. For example, that office could be a real problem for an American truckers’ strike.
Trust me, Pete Buttigieg is not here to fix the roads. He is a typical communist control freak who is going to take our freedoms away if we don’t take him seriously.
And taking Pothole Pete seriously is hard. Because on the surface, the guy is SUCH a DOUFUS.
He wouldn’t hurt a fly – right?
So when this infuriating poser bicyclist idiot does something like this…..
…..one is tempted to view this as merely stupid and impossible.
DO NOT make that mistake.
“Zero traffic deaths” is not only a fundamentally and intentionally MISDIRECTED GOAL that has a “feel-good” appearance of self-justification – which leverages our wish to “do the impossible” – it is CODE for all of the following:
personal transportation for the elite only
Mercedes for the elite – Chinese Trabants for luckier serfs
where you live becomes determined by your job
Soviet-level, corrupt, inefficient public transit for plebes
no freedom of movement – internal passporting
omnipresent cameras and surveillance, just like China
TSA internal control, “papers, please”, and all the rest
This is how these ASSHOES bring CHINA to AMERICA.
Zero traffic deaths is just like MOAR ANTIBODIES.
A PHONY and MISLEADING GOAL.
Now, before we get to the fact that we simply have to stop this crazy commie twerp, you need to know him better.
A great AUDIO will help.
Notice how PRESCIENT this talk is, right at the beginning.
You will ALSO love the end, when you realize that TRUMP is headed straight into confrontation with this joker.
Newly Uncovered COVID Vaccine Contracts Lead Unexpectedly to Academic Corruption and Shill Science Attacks on Honest, Skeptical Scientists
A Gail Combs deep dive into a tangent of Karen Kingston’s latest revelation on Pfizer Comirnaty vaccine deaths and injuries, leads back to the war against truth-telling doctors and scientists – this time by their own CORRUPT university employers.
PREFACE by Wolf Moon
Remember people saying that there was no such thing as the “FDA-approved” Comirnaty version of the Pfizer vaccine in existence?
Well, it turns out that REAL, LIVE COMIRNATY is out there, it has already killed over 50 people [in VAERS – yeah – do the math – x20 (1000), x40 (2000), or x100 (5000)], and – now even more shocking – there was some kind of bureaucratic screw-up in the contract and approval process which makes Pfizer LIABLE for all the deaths and injuries.
Look – I don’t know about the latter part – that’s “the law”, which is basically filled with LIES at this point. Whether any of these people will ever answer for anything is highly debatable, in my opinion.
But that’s not where this goes.
Gail Combs started looking at this video, and discovered ANOTHER scandal – the fact that universities which are silencing and firing honest doctors and scientists are not doing so from some misperception or moral high ground. These universities are turning on honest doctors and scientists because the universities themselves are COMPROMISED – by money, corruption, and the involvement of OTHER scientists at those same universities in the “scamdemic”.
We don’t yet know how deep this goes, but we do know this – the universities are clearly in cover-up mode. It’s not just limited to the vaccines. Fauci’s horrifying executioner remdesivir was forwarded past Trump, thanks to “work” done at one such university.
Follow along with Gail and you’ll see the SHAME of what has happened to many American universities, once bastions of free thinking and HONESTY – now CORRUPT and enemies of TRUTH.
-Wolf
START HERE….
FDA Broke Pfizer’s EUA Shield: Liability Protection Gone, Time To Bring Down The Gavel (10 minutes)
Stew Peters interviews former Pfizer employee and analyst Karen Kingston, who does deep dives into patents and contracts. She found the three major contracts for Moderna, J&J and Pfizer.
Stew: “Karen says she found contracts showing the DOD was in control of what data went to the FDA from vaccine trials. If that is true, then DOD not Big Pharm, was the central figure in any vaccine cover-up…. Military leaders maybe exposed as well…. When the FDA approved the Pfizer vax under the name Cormirnaty, it somehow broke their immunity shield.”
That is not exactly correct. DOD delegated it to Pfizer. With the Pfizer contract with the US Army, it appears that, it was delegated to Pfizer to have the ability to manipulate the data that was submitted to the FDA.
With the Moderna contract for example it shows HHS [US Dept of Health & Human Services] had the authority to manipulate the data that was submitted to the FDA. The contract date is 4/03/2020 for ½ billion $$$ with NIH subsidizing a lot of the contract. It was for producing 100 million mRNA vaccines. The contract (shown) states:
* Contractor shall submit draft FDA submission to BARDA at least 15 days prior to FDA submission
* BARDA will provide feedback to Contractor within 10 days of receipts
* The Contractor MUST address, in writing its consideration of all concerns raised by BARDA prior to FDA Submission.
NOTICE THE DATE 4/03/202. No wonder they wanted to kill HCQ in April!
Karen goes on to say that the contract says that BARDA can provide EDITS to the Data and THAT gets submitted to the FDA. She has never seen anything like this before. This [editing] is why the data was so phenomenally positive. This explains why the Whistle Blowers at Ron Johnson’s Formun found the DOD data had been ‘edited’ to remove the tons of adverse events.
She also said a lot of that contract is redacted including the Key personnel at BARDA .
The J&J contract of an mRNA vaccine was signed 08-Apr-2015 and 60 out of the 90 pages are redacted.
She then goes into the most recent contract. It is a joint mission of Dept of Defense and Dept of Health & Human services who contract with Pfizer/BoiNTech “for the co-development and distribution (excluding China) of a potential mRNA-based Coronavirus vaccine aimed at preventing Covid-19 infection“….. LOTS OF REDACTION….
The Research Collaboration & License Agreement by and between PFIZER INC. and BIONTECH RNA PHARMACEUTICALS GmbH [Germany] and BIOTECH AG July 20, 2018
Again the DATE July 20 2018 shows mRNA vaccines for the next outbreak of Covid WAS A DONE DEAL!
@5:00 Karen EXPLAINS the OOPS in the Contract. You can not have a contract for commercialization WITHOUT A FDA APPROVAL DATE!!! So how in Hades did they KNOW there would be FDA APPROVAL? This shows it was PRE-PLANNED IN 2018.
@7:00 She also found the Cormirnaty lots used in the USA and the VAERs data
The Biomedical Advanced Research and Development Authority (BARDA), within the Office of the Assistant Secretary for Preparedness and Response in the U.S. Department of Health and Human Services, provides an integrated, systematic approach to the development of the necessary vaccines, drugs, therapies, and diagnostic tools for public health medical emergencies such as chemical, biological, radiological, and nuclear (CBRN) accidents, incidents and attacks, pandemic influenza, and emerging infectious diseases.
Together with our industry partners, BARDA promotes the advanced development of medical countermeasures to protect Americans and respond to 21st century health security threats.
A part of the U.S. Department of Health and Human Services, NIH is the largest biomedical research agency in the world
So there is your Fauci connection.
And that brings me to the digging I have been doing.
I start with the Chair of the COVID VACCINE ADVISORY BOARD, Hana El Sahly, M.D. of Baylor College of Medicine. She is the one who wrote the Remdesivir paper for Fauci, just in the nick of time so he could get that toxin approved for the use in hospitalized elderly Covid patients.
Baylor College rang a major bell with me. This Yahoo News articles shows why:
Dr. Peter McCullough is being sued by the healthcare system that just mandated 40,000 employees to get the jab, and they’re doing it out of spite. Here’s the list of emails to those targeting him, if you wish to let them know how you feel….
Sidebar by Wolf – Dr. McCullough on Stew Peters
I dare anybody to watch this and find anything wrong with anything that Peter McCullough is saying. He is basically admitting – at a time when social media was still removing people for saying as much – that the vaccines seemed to no longer be working. And NOW we know why – because of the delta variant.
Dr. Peter McCullough, a Dallas cardiologist who is largely discredited by the scientific community [Remember Dr McCullough is the MOST PUBLISHED AUTHOR OF SCIENTIFIC PAPERS IN THE USA.] for his assertions that the COVID-19 vaccines are unsafe and that early treatment options have been suppressed….
While McCullough said that doctors were probably afraid to show up to the event, one of Oklahoma’s top infectious disease physicians, Dr. Anuj Malik, director of infection prevention and control at Ascension St. John, said that the doctors he spoke to were not afraid to attend. They were just not interested in sitting through what would be seen as a “politically-motivated, ideological speech by a modern-day quack.”
Malik said. “With all due respect, none of McCullough’s ideas have been supported by any randomized, double-blind, controlled clinical trials,” [<=== THIS IS ALWAYS THE EXCUSE! NO data is allowed except that PAID FOR BY BIG PHARMA/NIH.]
McCullough shared what he said was a threatening letter from the American Board of Internal Medicine warning that he could lose his certification for spreading misinformation. There is likely a good reason for his concern about losing certification. A Dallas County court granted a temporary restraining order against him in July on behalf of Baylor Scott & White Health for continuing to claim titles, including vice chief of internal medicine at Baylor University Medical Center, even after he was fired from Baylor in February. In addition, an article in Medscape, an online global news source for physicians and healthcare professionals, reported that Texas A&M College of Medicine, Texas Christian University and University of North Texas Health Science Center School of Medicine have also cut ties with McCullough for spreading misinformation….
>
So the Baylor Connection made me curious.
And looky what I found! No wonder Baylor sued Dr McCollough in the hopes of shutting him up as they entice people to be lab rats!
Researchers at the Vaccine and Treatment Evaluation Unit at Baylor College of Medicine have launched a clinical trial to study the safety and efficacy of a booster dose of the Moderna-mRNA-1273 COVID-19 vaccine…. The study is being conducted by the Infectious Disease Clinical Research Consortium in collaboration with the National Institute of Allergy and Infectious Diseases, part of the National Institutes of Health…. “It’s important to determine the magnitude of the immune response after a booster dose in persons who received different vaccines in their initial vaccine regimen. We will also be looking at the safety of a booster dose,” said Dr. Robert Atmar, professor of infectious diseases at Baylor and co-principal investigator of the national study.
This activity is supported by the Infectious Diseases Clinical Research Consortium (IDCRC) through the National Institute of Allergy and Infectious Diseases (NIAID) (UM1AI148684). The IDCRC, consisting of the Vaccine Treatment and Evaluation Units (VTEUs) and the IDCRC Leadership Group, was formed in 2019 to support the planning and implementation of infectious diseases clinical research that efficiently addresses the scientific priorities of NIAID. The consortium includes infectious diseases leaders and clinical researchers from Emory University, University of Maryland School of Medicine, Baylor College of Medicine, Cincinnati Children’s Medical Center and University of Cincinnati, FHI360, Fred Hutchinson Cancer Research Center, Johns Hopkins University, Kaiser Permanente Washington Health Research Institute, New York University, Saint Louis University, Vanderbilt University Medical Center, University of Alabama at Birmingham, University of Rochester, University of Washington, and NIAID. For more information about the IDCRC, please visit www.IDCRC.org.
With presentations from members of the NIAID, the Infectious Diseases Clinical Research Consortium (IDCRC) Leadership Group, and VTEU PIs, the inaugural meeting of the IDCRC began with opening remarks from Anthony Fauci, MD, NIAID director. Session topics featured details on working with the NIAID, the Division of Microbiology and Infectious Diseases, and grants management. Breakout sessions facilitated thoughtful discuss on the consortium’s scientific agenda, flu, STIs, malaria, enteric, and emerging diseases, mentoring and career development, special populations, emerging lab sciences, and operations.
The IDCRC institutions are leaders of influential infectious diseases, immunology and clinical research programs focused on vaccines and STIs at eight top academic institutions and affiliates across the country. The programs, faculty and collaborators at these institutions have exceptional NIH/NIAID network and international connectivity, a history of performing outstanding ID clinical research and the experience and capability of rapidly responding to ID threats.
Dr. Atmar is a member of the Baylor Vaccine Research Center and the federally funded Vaccine Treatment and Evaluation Unit (VTEU). This research group performs Phase I to Phase IV studies of experimental and licensed vaccines, and Dr. Atmar serves as Principal Investigator or Co-Investigator for the clinical trials. Dr. Atmar and the research group have been involved in important studies that led to the licensure of live attenuated and high dose inactivated influenza virus vaccines. They also have performed many studies evaluating vaccines targeting pandemic influenza, including H5N1, H9N2 and H7N9 viruses, and they have evaluated methods to improve vaccine immunogenicity, including delivery of vaccine by different routes of administration, different dosages, and with different adjuvant preparations. The group has also evaluated vaccines targeting other pathogens, including those with importance to biodefense.
Pajon R, Doria-Rose NA, Shen X, Schmidt SD, O’Dell S, McDanal C, Feng W, Tong J, Eaton A, Maglinao M, Tang H, Manning KE, Edara VV, Lai L, Ellis M, Moore KM, Floyd K, Foster SL, Posavad CM, Atmar RL, Lyke KE, Zhou T, Wang L, Zhang Y, Gaudinski MR, Black WP, Gordon I, Guech M, Ledgerwood JE, Misasi JN, Widge A, Sullivan NJ, Roberts PC, Beigel JH, Korber B, Baden LR, El Sahly H, Chalkias S, Zhou H, Feng J, Girard B, Das R, Aunins A, Edwards DK, Suthar MS, Mascola JR, Montefiori DC.
N Engl J Med.
And the Affiliations:
• Moderna, Cambridge, MA. • National Institute of Allergy and Infectious Diseases (NIAID), Bethesda, MD. • Duke University Medical Center, Durham, NC. • NIAID, Bethesda, MD. • Emory University School of Medicine, Atlanta, GA. • Fred Hutchinson Cancer Research Center, Seattle, WA. • Baylor College of Medicine, Houston, TX. • University of Maryland School of Medicine, Baltimore, MD. • National Institutes of Health, Bethesda, MD. • Los Alamos National Laboratory, Los Alamos, NM. • Brigham and Women’s Hospital, Boston, MA. …..
Atmar RL, Lyke KE, Deming ME, Jackson LA, Branche AR, El Sahly HM, Rostad CA, Martin JM, Johnston C, Rupp RE, Mulligan MJ, Brady RC, Frenck RW Jr, Bäcker M, Kottkamp AC, Babu TM, Rajakumar K, Edupuganti S, Dobrzynski D, Coler RN, Posavad CM, Archer JI, Crandon S, Nayak SU, Szydlo D, Zemanek JA, Dominguez Islas CP, Brown ER, Suthar MS, McElrath MJ, McDermott AB, O’Connell SE, Montefiori DC, Eaton A, Neuzil KM, Stephens DS, Roberts PC, Beigel JH; DMID 21-0012 Study Group.N Engl J Med.
Affiliation • From the Departments of Medicine and Molecular Virology and Microbiology, Baylor College of Medicine, Houston (R.L.A., H.M.E.S.), and Sealy Institute for Vaccine Sciences, University of Texas Medical Branch, Galveston (R.E.R.); the Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore (K.E.L., M.E.D., K.M.N.), and the Division of Microbiology and Infectious Diseases (S.C., S.U.N., P.C.R., J.H.B.) and the Vaccine Research Center (A.B.M., S.E.O.), National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda; Kaiser Permanente Washington Health Research Institute (L.A.J.), the Departments of Medicine (C.J., T.M.B., M.J. McElrath) and Laboratory Medicine and Pathology (C.J., C.M.P.), University of Washington, the Vaccine and Infectious Disease Division (C.J., C.M.P., C.P.D.I., E.R.B., M.J. McElrath) and the Statistical Center for HIV/AIDS Research and Prevention (D.S., J.A.Z.), Fred Hutchinson Cancer Research Center, and Seattle Children’s Research Institute (R.N.C.) and the Department of Pediatrics (R.N.C.), University of Washington School of Medicine, Seattle; the Department of Medicine, Division of Infectious Diseases, University of Rochester, Rochester (A.R.B., D.D.), NYU Langone Vaccine Center and Division of Infectious Diseases and Immunology, Department of Medicine, NYU Grossman School of Medicine, New York (M.J. Mulligan, A.C.K.), and NYU Langone Hospital-Long Island Vaccine Center Research Clinic and the Division of Infectious Disease, Department of Medicine, NYU Long Island School of Medicine, Mineola (M.B.) – all in New York; the Departments of Pediatrics (C.A.R.), Microbiology and Immunology (M.S.S.), and Medicine (S.E., D.S.S.), the Center for Childhood Infections and Vaccines (C.A.R.), Hope Clinic of Emory Vaccine Center (S.E.), Emory Vaccine Center, and Yerkes National Primate Research Center (M.S.S.), Emory University School of Medicine, Emory University, and Children’s Healthcare of Atlanta (C.A.R.) – all in Atlanta; the Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh (J.M.M., K.R.); Cincinnati Children’s Hospital Medical Center, Division of Infectious Diseases, University of Cincinnati College of Medicine, Cincinnati (R.C.B., R.W.F.); and FHI 360 (formerly Family Health International) (J.I.A.) and Duke Human Vaccine Institute (D.C.M.) and the Department of Surgery (D.C.M., A.E.), Duke University Medical Center, Durham, NC.
Hana M. El Sahly, MD is principal investigator for Baylor and under her is listed Jennifer A. Whitaker, C. Mary Healy, Christine Akamine, Wendy A Keitel, Robert L Atmar, Annette Nagel, Sandra Francisco, Thea Marie Cordero, Janet Brown, Jennifer Christensen, Caroline Doughty-Skierski, Connie Rangel, Carrie Kibler, Coni Cheesman, Lisreina Toro, Chanei Henry, Chianti Wade Bowers, Pedro Piedra, Kathy Bosworth, Kayla Burrell, Jesus Banay, Tykel Eddy, Trent Davis, Shetel Anassi, Yvette Rugeley, Olga Rybina-Willis …..
So what about the OTHER 15 on the ‘Advisory Board’ I checked, none are in the COVE study group.
Wang EW, Parchem JG, Atmar RL, Clark EH.Open Forum Infect Dis.
2021 Apr 10
Abstract As the first severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines passed UK and US regulatory milestones in late 2020 and early 2021, multiple professional societies offered recommendations to assist pregnant and breastfeeding people as they choose whether to undergo vaccination. Despite such guidance, the lack of data describing vaccine safety, immunogenicity, and efficacy in pregnant and breastfeeding people has made this decision challenging for many. However, even considering the paucity of data, the known risks of coronavirus disease 2019 during pregnancy likely outweigh the not yet fully elucidated risks of SARS-CoV-2 vaccines, which have reassuring safety and efficacy profiles among nonpregnant people.
The Chair of the FDA Vaccines and Related Biological Products Advisory Committee is so compromised she should NEVER have been anywhere near the approval process!
-GC
Summary
After viewing the tape of Dr. Peter McCullough on Stew Peters, I’m both shocked and disappointed that Baylor (IMO both the College of Medicine and the allied University) would do anything except DEFEND Dr. McCullough for simply speaking TRUTH when nobody else dared to say it.
At a time when all of social media was defending what now amounts to SCIENTIFIC ERROR, Baylor – a renowned institution – accused a TRUTH-TELLER of “misinformation” for being on the cutting edge.
To borrow from Trump…… “SAD!”
We know now that everything Dr. Peter McCullough said was not only true, but that the science he cited was LEADING EDGE – pointing in the direction of future findings.
It is not “misinformation” to state scientific and medical findings which are both TRUE and in the process of CHANGING narratives. That IS what science is supposed to do.
China won’t have to fire a SHOT to steal academic leadership from the United States, if Baylor – in TEXAS of all places – is going to hand them scientific superiority on a silver platter.
Get the politics and the self-dealing OUT OF YOUR SCIENCE, BAYLOR.
It is a TRAVESTY for you, Baylor, to let your “big money scientists” force out your TRUTH-TELLERS based on POLITICS and motivated by their own SCIENTIFIC MISJUDGMENTS.
