“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
The term “clot shot” was one of the absolute BEST memes that this site has ever promoted. I personally picked it up off of Aubergine, if I remember correctly. That term – I am quite certain – saved THOUSANDS of lives – maybe MILLIONS.
The problem?
That name needs an upgrade. We have NEW PEOPLE TO SAVE.
We are now very certain that the mRNA COVID vaccines cause significant immune problems in recipients.
I was first convinced of this by the report from Dr. Nathan Thompson.
Fauci and Pfizer have painted themselves into a bit of a corner. I now believe that they “played a charade” on boosters – that boosters were their intent all along. I think this WHOLE scam was very intentional. But it gets far, far worse. I think I see that they have an agenda much bigger …
Official Government of Canada data is truly terrifying; it suggests the Triple Vaccinated have developed AIDS & are now 5.1x more likely to die of Covid-19 than the Unvaccinated
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.
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!)
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.
It’s GALLERY NIGHT, wherein our intrepid “print screen photographer” and “substitute bartender” presents his “artistic screen shots” of the Defeat The Mandates rally in Washington, DC.
While our beloved REAL bartender takes a needed break of unknown duration, we will continue to ENDEAVOR TO PERSEVERE.
Tonight’s drink special is not ethanol, but rather a different alcohol – epinephrine – a.k.a. – ADRENALINE.
Stay tuned! We’ll explain later!
Christmas Spirit
It looks like SANTA is still somewhere NORTH of the border, but he’s bringing FREEDOM!
(Hat Tip Sundance via DDG)
Playing on the Jukebox
Well, we were looking for some stuff that was COMPLETELY DIFFERENT on the persnickety jukebox, and look what we found near the end of the last slider…..
EPIC COWBOY/WESTERN ROCK.
What the FREAKIN’ ‘ELL.
https://youtu.be/I8gr2hmIbew
Not sure what’s wrong enough with me to like this, but if you don’t enjoy this crazed version of cowboy, try an even crazier version of “Indian”.
And I mean that BOTH WAYS.
This stuff looks straight out of Burning Man.
And while that’s kind of interesting, it’s not about the kind of FREEDOM that goes with the ART on the wall tonight.
SO – we add some EPIC FREEDOM MOOD MUSIC for your GALLERY TOUR tonight.
That’s more like it.
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.
And in the following video, you can actually hear the HOWL of WOLF MOON, telling MAFIA NAN exactly how he felt, when her Praetorian guard fired GRENADES upon a crowd filled with GRANDPARENTS, WOMEN and CHILDREN on January 6.
The Truth About Our January Sixth Protest I was there, and I am PROUD of it. I am proud of the thousands and thousands of patriots who showed up to make an historic statement that the other side could only TRY to stop, by besmirching its beauty with their LIES and TRICKERY. Yes, their LIES …
Current Art On The Wall
We have a really interesting PHOTOGRAPHY exhibit in the bar this week. Consider this to be “gallery night”.
Prints are available FREE by right-clicking – or whatever you need to do on your device.
We have more pictures than just this collection, but these are some of the best. Enjoy a selection of magical moments from the DEFEAT THE MANDATES rally in Washington, DC last Sunday.
Dr. Heather Gessling
Dr. Lynn Flynn
Looking for this lady’s name!
Looking for this gal’s name, too!
Ernest Ramirez (vaccine injured and lost son)
And over in the corner, THIS RIGHTEOUS RANT is playing on a loop on our FREEDOM TV.
If you haven’t seen it, watch it. If you have seen it, watch it AGAIN!
One of the thing that tells me science is really out of whack right now, is the fact that scientists are discouraged from doing simple, plain-Jane things that would actually make vaccines safer for the general public, but are instead encouraged to go off in other, riskier, sexier, more profitable directions, while protected by a kind of “media umbrella of propaganda” which justifies, and rationalizes, but does not convince the HONEST skeptic and investigator.
In a sense, we still have the same sort of “patent medicine killers” of the late 19th century, with their poisonous potions – we’ve just changed WHO it is who is allowed to kill people and make money with bad medicines.
The fact that the very first COVID vaccines were of a risky, barely understood, and rather experimental type (mRNA or viral vector, i.e. genetic, full spike, in humans), while EASIER, FASTER, CHEAPER, SAFER, and much more familiar and better-understood vaccine types (protein or glycoprotein antigen, subunit) were IGNORED and SLOW-WALKED until later – well, it would have boggled my mind a long time ago, but no longer.
In my opinion, the “science”, if you can call it that, was guided by FAUCI PATENTS, rather than by what would have been best for patients AND for vaccine science.
The point about damage to vaccine science ITSELF is a point that Robert Malone often makes, which is critical. The people behind the bad, biased, self-interested, money-making vaccine choices, didn’t just screw THE PEOPLE – they screwed up the SCIENCE.
Let me be blunt. When people LIKE ME attack Tony Fauci, we’re not attacking science.
We’re attacking ABUSE OF SCIENCE by an OUT-OF-CONTROL BUREAUCRAT, aided by MERCENARY GLOBAL CORPORATIONS.
Tony Fauci is biased and corrupted by many sick and damaging compromises and ties to the industry he is SUPPOSED to be countering when necessary on America’s behalf – NOT coddling at every personally beneficial turn.
And all of this WRONGNESS was created under the cover of Francis Collins, who was used as a very phony TOTEM of “ethics” and “morality”. The man was pimped to the masses as a great Christian, as if that meant he WOULD and COULD do something about bureaucratic ethics and morality, while those very virtues he was meant to represent but not interfere with, were UNDONE by a series of corrupt administrations.
There is a LOT that is wrong with government regulation of science and medicine right now, and we need to talk about it.
Tonight, I’d like to talk about just ONE point of vaccine science which is weirdly out of whack, and protected ONLY by propaganda – and that is vaccine localization.
That means MAKING THE VACCINE STAY PUT WHERE YOU INJECT IT.
Obviously this is not working. OK? I’ll just be blunt.
One of the points frequently made against actual science on social media, mostly by CCP propagandists, IMO, is that vaccines simply do not leave the injection site, and thus all these systemic and distant effects which people allege to have been caused by vaccines, could not possibly have been caused by the vaccines. I saw this canard far more often than I should have, because people, generally, are not prepared to debate it.
Even when people just argue the evidence back and forth, because the reality is fuzzy and moves around between “localizes” and “migrates”, the argument itself is a fantastic deflection by the “protectors of vaccines”. Instead of talking about the very real problems caused by even LIMITED MIGRATION of vaccines, we’re one step removed from the problems.
These sorts of arguments – that the spike protein vaccines could NOT be migrating from the injection site – were completely undone by the Pfizer data obtained from Japan.
Yes, it was animals, and yes, it was perhaps at an over-sized dose, but the numbers themselves were SO substantial that these kinds of factors basically “factor out”. There is NO DOUBT from this data that there is a RISK of migration of “vaccine which infects cells and cranks out [highly pathogenic] spike protein which is HOPEFULLY dealt with cleanly by the immune system”.
The propaganda that vaccines don’t migrate was CLEARLY violated by the case at hand. That propaganda disappeared rather quickly, although I still hear it from nurses, and just bite my tongue.
Further – shockingly – the idea that the lipid nanoparticles containing the vaccine mRNA (basically what are called “virus-like particles” when injected as part of wasp venom) could actually have time to persist as part of skin lipids and BE SHED – well, it’s rather obvious from the data that this is a very real possibility.
The SKIN is an organ just like everything else. Everything else meaning all the OTHER organs that were getting the vaccine mixed into THEIR lipids in shocking amounts for a very long period of time.
Suddenly the CRAZIEST of the conspiracy theories about the mRNA vaccines was LITERALLY – and I mean LITERALLY – biophysically possible.
I had previously come up with a marginally feasible idea that maybe the spike protein itself was not just toxic, but HORMONE-LEVEL ACTIVE, to explain what people were reporting. But with the Pfizer data, I didn’t need any of that. The VACCINE ITSELF was ready to be shed.
And Pfizer hid this. Yeah. I can kinda see why.
So – if I may – let’s just set aside this foolishness that vaccines don’t migrate, and never have systemic or distant effects, because they do. It’s VARIABLE, but it’s REAL.
So why don’t people DO anything about this?
Why not do things that would absolutely ensure that vaccines CANNOT leave the injection site?
I can imagine a lot of things that MIGHT do this, but had never heard about any adjuvants or additives or vaccine designs that could effectively localize vaccines to arm or shoulder muscle, and simply make sure they didn’t migrate to even the slightest degree.
Solve THAT problem and pericarditis is GONE – RIGHT?
So why not do it? And why not BRAG about it if you CAN do it? Why not say how it’s done?
CRICKETS.
FAST FORWARD to a recent bit of knowledge that I happened upon IN REAL LIFE.
I noticed that I was somewhat jittery after having some minor dental work done. I was quite numb for the work, but later, after leaving the dentist’s office, with the numbness now faded, I noticed that I was shaky, edgy, and “wired”. That went away over the rest of the day. I just assumed that it was a side effect of the anesthetic.
I mentioned this to an anesthesiologist and a nurse, who both explained to me that it was NOT due to the anesthetic, but rather to epinephrine, which is sometimes ADDED to an injectable anesthetic in order to LOCALIZE it.
They explained to me that by epinephrine constricting the blood vessels in the region where the anesthetic is injected, the body removes less of the anesthetic by drawing it away in the blood stream – so the anesthetic STAYS at the site of the injection, giving a longer duration of anesthesia.
Sure enough, when I looked this up online, I found out it is quite real.
So I immediately thought to myself – why not do the same thing with vaccines?
Why not try to localize them with something like epinephrine?
But when I looked THAT up, the only results that I got, were for use of epinephrine (you know, as in the EPI PEN) in treating anaphylactic reactions TO vaccines. I probably didn’t look hard enough, but I’m not trying to get a patent or anything like that.
So who knows? It may be that adding epinephrine to vaccines could actually be GOOD in terms of reducing the severity of anaphylactic reactions – in addition to localizing the vaccine.
However, the possible technical feasibility of doing something isn’t my point.
My main point is simply ADMITTING THERE IS A PROBLEM.
If you could simply make these DAMN mRNA vaccines STAY where you put them, and if they didn’t crank out a bunch of bad stuff into the blood stream, then perhaps the only long-term risk would be something like cancer AT THE SITE OF INJECTION.
However, let’s be real. Nobody even TALKS about the problem. The media just DENIES IT.
In my opinion, “they” aren’t addressing this problem, because it gets on the way of “their” real purpose or purposes.
Vaccine localization is the last thing that these people wanted to “solve” here.
The people who CONTROL science and medicine don’t have to tell us about their entire agenda. They only have to tell us things that are somewhat plausible and rational.
In my opinion, mandatory vaccination is a PLATFORM for SOCIALISTS to do whatever they want to whomever they want. It gives them cart blanche to change society without accountability. That is the big picture, and has been their objective for well over 100 years.
Look at what communists are doing to Uighurs in Communist China RIGHT NOW.
They want to experiment on you, they experiment on you.
They want to kill you, they kill you.
Doing things which do not contribute to, or which would actually IMPEDE their “unholy grail” goal of direct control over humans, is simply NOT going to happen, if THEY can help it.
But that doesn’t mean that WE can’t give them a BAD HAIR DAY, EVERY SINGLE DAY, and fight for WHAT IS RIGHT in science and medicine.
defederalization of science
destalinization of medicine (de-obamatization in practice)
force ethics and transparency where socialists don’t want them
bring anti-deception tools and language INTO science itself
chase politics out of science, acting in both of them
We knew it was a snake when we let it in. Now, we all have to kick it out.
In which I argue that WE are the new cell culture for an uncontrolled gain of function experiment, that only WE can end.
It took me a while to figure out WHY they insisted on using the FULL SPIKE PROTEIN for these damn vaccines. This question has bugged me from the very beginning, and it got worse and worse as more and more spike protein side effects piled up.
Thankfully, sleeping late on the morning of 9/12/ 21, I had a DREAM which finally helped me see the answer.
It wasn’t exactly Kekulé’s dream, but it served the same purpose – to accept what I had not yet been able to fully see and accept.
Now, normally I would not mention that ANY of this came from a dream. There is no faster way to lose credibility, than to say “it came from a dream” – other than saying the answer came from the voice of God. But the truth of the matter is that I often find that UNRESOLVED QUESTIONS form what might be called “motifs” in my dreams, and sometimes I actually get some kind of resolution FROM the dreams.
If I tried to explain the dream itself, it would be almost meaningless to you. Things shift and change in dreams. Stone becomes brick becomes concrete and then vanishes. Stairs appear and disappear. People are there and people are gone, to be replaced by different people. One location changes smoothly into another location.
All of THAT is a jumble. This dream was a real doozy, too. Crazy! But in the dream I kept trying to resolve something – actually TWO things – which were composed of collections of ideas. These two things were like little, linear, diagrammatic collections of jewelry boxes, and it was impossible for me to SAY anything useful about the two collections, and how they related to each other, without actually interacting with them and looking into the jewelry boxes in some fashion or another, and in doing so, the collections were no longer separated and isolated from what might be called “everything else”.
It was IMPOSSIBLE for me, in the dream, to separate these things from “everything else”, if I wanted to know anything about their reality.
When I woke up, I realized the point of the dream.
The point of the dream was that the two things – IN REALITY – were both connected not only to each other, but to everything else. The point of the dream was that I needed to look at how the two things EACH interacted with everything else, to see how they were TRULY related to each other.
Not how they were SUPPOSED to be related to each other, but how they are ACTUALLY related to each other.
And THEN – in the “generality” of that moment – I realized that this “model”, if you will, applied to the COVID-19 VIRUSES (one collection) and the mRNA VACCINES (the second collection). And in THAT moment, I stopped looking at them as ANTAGONISTIC things, just because a LIAR named Fauci says they are antagonistic, but instead as SIMILAR and COMPLEMENTARY things.
As genetic material.
THAT is when “IT” hit me.
I woke up fully, and realized the following.
The VIRUSES and the VACCINES are DESIGNED to interact with each other in the realm of “everything else”, that being us humans. They are NOT designed to interact in the way we are being told. They are designed to interact in the way that they ACTUALLY DO interact.
Let me give you a simple representation of this relationship.
Consider a square. Color the top side GREEN – that represents “everything else”, not as it “should” be, but as it REALLY IS. Every point on that line segment is part of the world, relating to other points in the ways that they REALLY DO, in a “green” way. It’s ALL GREEN.
Now make the bottom two CORNER POINTS the two collections. Connect those points to the top of the square by green lines – the left and right sides of the square. Again, this is how they REALLY connect.
We are being TOLD that the bottom side of the square is RED.
Why should we believe that? What if it’s NOT red? What if it’s GREEN? What if there is a simpler GREEN ANSWER?
And IMMEDIATELY I knew what the GREEN ANSWER WAS.
The mRNA “vaccines” encoding a spike protein are designed to do in HUMANS containing the virus exactly the same thing that similarly added spike protein mRNA does in CELL CULTURES containing the virus. They are designed to CHANGE THE VIRUS – to make it GAIN FUNCTION. ALL that is needed to create the new virus is an otherwise identical injection with a NEW CODE that GAINS FUNCTION.
In other words, genetic vaccines offer an opportunity to smoothly regulate the rate and direction of evolution of the virus, without humanity knowing it. And they do it IN THE ANIMAL HOST INTENDED.
This solved many mysteries, which I will explain shortly.
This told me that there is ZERO need to go off and create a new variant in a lab. All one has to do is to change the code of the vaccine mRNA, and PRESTO – a new variant is introduced “in the wild”, with almost no chance of getting caught.
At this point, many of you are doing a WTF, so let me back up and explain this again.
What science does to “create a new virus” in the laboratory, from RNA or DNA, is to “somehow” (COUGH, COUGH, COUGH) get the RNA or DNA that they want to get into the NEW VIRUS, into laboratory cell cultures that are making OLD VIRUS. They need to get it into the cells, pretty much like they get the vaccine mRNA into our cells, using nanotech or virus vectors. THEN, the “old virus process” slips the “new genetic instructions” into the old protein shell, but as the virus spreads and multiplies, IF there is any “gain of function”, then the NEW INSTRUCTIONS in the NEW protein shell will WIN, and the result will be THE NEW VIRUS with GAIN OF FUNCTION.
Nobody really wants to spell out all the details of gain of function techniques in public, just like they don’t want to give the directions of how to make high explosives to terrorists. But THAT KNOWLEDGE IS OUT THERE, and we know roughly HOW THEY DO IT.
Honestly, it’s a bit like plant grafting, only instead of being largely in the Z DIRECTION (up), it’s in the T DIRECTION (time). You GRAFT new instructions into an old virus, until the new virus TAKES.
What they have done here is to create a PLATFORM for genetic change. Eventually it will be used to change US, but for the moment, they are clearly using it to CHANGE THE VIRUS (which is used to help change us, albeit somewhat indirectly).
Now – I said that this solved many mysteries. I’m going to list them here.
Why the full spike protein in the vaccines, despite its toxicity, and the greater likely safety of vaccines based on smaller subunits like the RBD?
Because the full spike is the main part of the virus that they’ve been changing, and which “gains function”. To get a new virus with a new spike, you have to change the instructions for the spike that get encoded in the virus. Also because you want to include the genetic instructions for ONE OR MORE FULL PIECES of the virus, if not the entire virus. That depends on exactly how the virus builds. We know (the Jaenisch paper) that the virus uploads fragments of its own RNA into the genomic DNA of the host, which come back out and are transcribed to RNA, so it will presumably do the same to pieces of the vaccine when both are present. Viruses that build from the vaccine spike variants will tend to WIN if they have gained function.
Why mRNA vaccines, despite the obvious safety advantages of protein vaccines?
Because protein is GENETICALLY SAFE – and that is NOT what they want. If the human population is now the experimental platform for virus gain-of-function experimentation, then only by being able to inject us with mRNA or DNA will viruses be able to be swiftly and decisively modified IN VIVO.
Short answer – they are not trying to change OUR genes yet – but they ARE trying to change viruses IN US. In vivo. And not in a way for our own good.
Why did they fight so hard against short-protein subunit vaccines like those from Winfried Stöcker and Sorrento?
Because if those vaccines are clearly superior to genetic vaccines due to safety or efficacy, then the conspirators will LOSE THEIR PLATFORM for genetic modification of viruses IN VIVO in the human population. Thus, these likely safer subunit and PROTEIN vaccines encountered delay after delay, and roadblock after roadblock, and in the case of the Stöcker vaccine, threats of arrest and legal trouble.
Why is Ralph Baric now doing work on chimeric mRNA vaccines that include LONGER mRNA encoding MULTIPLE proteins from SARS-CoV-2?
Because this approach toward longer and more mRNA leads closer to what they need to do – to inject us with the complete instructions for modified viruses – basically as what are called “virus-like particles” (VLPs), or by using viral vectors. These are “Fauci-compliant” in that they are “all about more and more antibodies”, and thus follow Fauci’s “antibody hypnosis” act, but clearly they will have more and more side effects, possibly including ADE.
As you can see, the vaccines are “less and less about natural immunity”, less and less about individual health, and more and more about experimentation and sociobiological engineering.
What does this have to do with Judy Mikovits?
Judy is one of the few people who have honestly explained the GAMES that the Faucists are playing with gain of function.
https://www.youtube.com/watch?v=0B17QQTr6xY
She explained that what these people have done – in complete violation of the CONTROLS that were placed on genetic engineering back in the 1970s – is to FORCE VIRUSES to “take” in human cells, allegedly in order to “see if they can or cannot take in human cells”. They are basically saying “we have to try hard to change the liquid to make the liquid catch fire, to see if it’s flammable”. This is a special kind of dishonesty.
There are MANY ways to make a virus “gain function”, but one of the FIRST and SIMPLEST is to just use tricks to make it change enough on its own, to eventually “take” in human cell culture.
It’s a lot like Nancy Pelosi and Obamacare – “you have to pass it to see what’s in it”. That is a special kind of cynical dishonesty, IMO.
But NOW they have actually HIDDEN gain of function research in PLAIN SIGHT. In us. Thanks to genetic vaccines.
Why did Adam Schiff go after Natural News and get them deplatformed?
Because the greatest danger to their plan is that humans will reject the future of human genetic modification IN VIVO. Natural News and their movement are a focal point of organized opposition. The Democrats KNEW this was coming, and they wanted the opposition out of the way.
This is also why so much work goes into discrediting these people.
But if the vaccine is for the SAME spike protein as in the virus, then how is THAT gain of function?
It’s NOT. It is ONLY if the vaccine contains DIFFERENT genetic material, DIFFERENT instructions, that any possibility for CHANGING the virus ensues.
Now tell me how you are going to go into EVERY vaccine that is given ANYWHERE in the world, and make sure that the mRNA doesn’t encode a new variant?
You can’t. That’s the evil genius of this plot.
If I want to introduce a variant ANYWHERE, all I have to do is give out a vaccine at the target location, where my vaccine looks just like the official stuff – or maybe even IS official stuff – but mine contains whatever genetic data is needed for a new virus, inside the same old nanotechnology.
You see – WE. HUMANS. OURSELVES. ARE. NOW. THE. GAIN-OF-FUNCTION. PLATFORM.
Pretty slick, if you ask me.
Could this platform be used for ADE as an intended effect?
Yes – because the variant that challenges prior antibodies is controlled by whoever launches the variant – and if that person or group is the same one controlling the vaccines, then TOUGH LUCK. And the ADE could be pinpointed in space and time, pretty much like Stalin’s Holmodor against the middle class in Ukraine. This platform of viral control can be used to control people at the individual, family, local, regional, state, national, continental, and global levels.
If we stop using these vaccines, will the variants stop?
They might stop. It will become much harder for the variants to appear, whether they are natural, and arise from vaccine evolutionary pressure, or are man-made, and require the vaccines for delivery.
Some of the best early opinions, IMO, thought that the initial genetic drift of SARS-CoV-2 was sufficiently small, that a single vaccination would cover all likely variants. While I’m not highly confident in that thought any more, I think it indicates that drift would be small, were it not for the vaccine.
So which is the plot – the virus or the vaccine?
AND logic – it’s BOTH OF THEM – the message of the dream. And it’s BOTH OF THEM in the SAME context that it would be in HUMAN CELLS. We are just “human cells on the hoof”.
The virus is out – and now they can change it “in the wild” thanks to GENETIC VACCINES – the greatest cover for genetic experimentation on viruses and humans that was ever conceived.
So how do we stop this plot?
Easy. We utterly reject genetic vaccines as a RISKY PLATFORM FOR TREATING VIRAL DISEASE, because they can be used to manipulate the disease and the diseased. The risks are not just individual – they are SOCIETAL as well. So we make them highly illegal. To get there, we use CIVIL DISOBEDIENCE FIRST. We REFUSE genetic vaccines.
For those who want vaccines, we go to old-school, time-tested, PLOT-SCUTTLING, protein vaccines. And all VOLUNTARY.
We don’t call this a RELIGIOUS objection. We are honest and call it a MORAL OBJECTION. If, however, your CHURCH OR SYNAGOGUE takes up the sword of abolition, and adheres to the morality of rejecting genetic vaccines, e.g., as considering them a form of “tempting the devil”, then you CAN validly call it a religious objection, too.
However, as an ETHICAL objection, like the objection to SLAVERY, all humans can take part.
Make no mistake – we are now in a literal HUMAN GAIN OF FUNCTION EXPERIMENT, using the whole human population as test subjects, and genetic vaccines as the obvious GOF vector.
The only way to STOP THE EXPERIMENT COLD, is to STOP USING GENETIC VACCINES.
Simple. Don’t let the snake in. Or if you HAVE let it in, kick it out!!!
Featured Photo: Meeting of the War Crimes Executive Committee, which decided on the arrangements for the Nuremberg trials. Note the garage pull in the background – Exhibit F1b.
I am dying of the China Virus. I had the virus itself in the latter half of January, 2020. I became symptomatic on January 18, and thus working backwards by 5 days, I estimate that I got it on January 13 – either from friends who had traveled internationally, or from documents they carried which had been handled by Iranians. I’ll never really know.
The only other person at that meeting who got the China Virus was my wife, who did not get it at the meeting, but later. It is likely that she got it from me on roughly January 19 or 20, given that she became symptomatic around the 24th or 25th.
My wife passed it to one other person, who passed it to their spouse, and that seems to have been the end of our chain.
For various reasons – otherwise known as comorbidities – I suffered hypoxia and lung damage, whereas my wife did not – nor did those who got it from her. Nevertheless, she does seem to have milder chronic effects such as peripheral pain and clotting issues, which could be related to the virus. Strangely, her prior problem with nose bleeds has vanished.
My wife’s symptoms were otherwise identical to mine except for hypoxia and lung damage. Both of us had the same “dry cough”, mild fever, exhaustion, weird headache and kidney aches, etc. She was also taking vitamin D for osteoporosis therapy – I was only taking a multivitamin with a low dose of vitamin D. I highly recommend vitamin D to prevent severe China Virus symptoms. I believe that it spared my wife.
My chronic symptoms are interesting. They are mostly cardiovascular, cerebrovascular, and pulmonary. You may learn more about them later in this article. I have some highly diagnostic clotting issues as well, which are specifically known to be RISKS for the coronavirus vaccines.
It is inadvisable for either me or my wife to take a coronavirus vaccine, given that I already have excellent immunity, the “clot shots” appear to degrade that immunity, and recoverees are 2 or 3 more likely to have side effects from “the jab”. That, in addition to my specific contraindications.
You will understand shortly that it would be MURDER to give me a coronavirus vaccine. It would also be MURDER to give my wife one. And to give one to a child, is going to be SCANDALOUS MURDER of the worst kind.
Consequently, I consider all people who want to give me, my wife, or anybody else, a coronavirus vaccine, as MURDERERS.
I do not consider such people, who would mandate a murderous injection – this really bad vaccine – to be much better than the CCP, the Nazis, or the Soviets.
So maybe by now you are STILL wondering – what is this “Nuremberg II” all about? Glad you asked.
My Nuremberg Wake-Up Call – Stew Peters
This tweet from Stew Peters, which I saw on Gab, really resonated with me.
During the Nuremberg Trials, even the media was prosecuted and put to death for lying to the public.
He’s not lying – I can show you pictures from the Nuremberg Trials.
Since Stew might get bounced from Lying Twitter any time, I save the above tweet as an image.
The only problem is that we ONLY prosecuted National Socialist Lying Press. We did NOT arrest Bolshevik Socialist Lying Press, who started the whole thing, by driving Germany INSANE.
My mother knew the Nazis as a child and a teenager. She dodged through their crazy system, growing up, doing whatever she needed to do, not to be killed. She had so many strikes against her, if anybody knew ALL OF THEM, she was as good as dead. Very few people knew ANY of her strikes. Only she and her family knew all of them. The family kept the most dangerous strike secret. You can now understand why my mother thought that FAMILY is so important.
My mother was classified as “racially impure”. That was not a death sentence – but if combined with other bureaucratic criteria, it could be. She was half-American – part American Indian – and her German side was “not pristine”. Her grandfather, still the family patriarch, was a Mason, but apparently had enough connections or excuses not to be arrested.
My mother was not brave like Sophie Scholl, the college student who was killed by Hitler for printing pamphlets criticizing the Nazis and their war crimes. No – my mother was a survivor. A very cunning one, cowardly one moment – brave the next, who stayed one step ahead of the Gestapo by learning to LIE her way through the system.
But what my mother DID do was to serve as a WITNESS TO HISTORY. She saw the Holocaust, and how REAL it was. She saw horrible things that she told me in great detail – so that SOMEBODY would remember.
Polish survivor Jadwiga Dzido shows her scarred leg to the court, while expert witness Dr. Alexander explains the nature of the medical experiment performed on her in the Ravensbrueck concentration camp. Dzido and Alexander were appearing as witnesses at the Doctors Trial.
The experiments were performed by defendants Herta Oberheuser and Fritz Ernst Fischer, on November 22, 1942.
Medical Socialism
In the 1970’s, I remember being in a car, laughing hysterically with a Jewish friend, smoking cigarettes, driving home from college, joking about the weird, occasional, bizarre, seemingly mentally ill “health nazis” who talked about regulating smoking and junk food. We knew this idiocy they dreamed of would never happen – COULD never happen. This was AMERICA. This shit does not happen in AMERICA. MAYBE in Russia. Definitely not in America.
Have another COKE! No Diet Coke here. Plenty of sugar for plenty of energy!
Banning smoking? BWAHAHAHAHAHA! Good one!
What’s next? Sugar? HAHAHAHAHAHA! Hilarious! These health nazis. They’re CRAZY.
Oh, my goodness. I was such a fool. I could NOT make the connection to my mother.
My mother’s big, deadly secret was a horribly deformed back, with one God-given blessing. It looked absolutely normal with clothes on.
She had learned over her lifetime to keep it a secret. She always dressed in the closet, with her back away from the door. I only saw it ONCE, by a combination of accidents, when, as an adult, she made the mistake of walking out of the closet to speak with my father, not having shut the bedroom door completely, not knowing I was still in the house, and I turned and looked through the slightly open door.
I was utterly shocked. It looked like something from the films Alien or Species.
My mother hid it through the entire Nazi nightmare, except when she was forced into one examination. The doctor saw her back – as he moved around her next to the wall – but he lied to the nurse and said she was fine.
There WERE good people – but they had to pick and choose the exact right moments to ACT AGAINST THE MACHINE.
And I’m here to tell you, EARLIER IS BETTER.
Here is how bad medicine got in Nazi Germany.
Between September 1939 and April 1945 the defendants Karl Brandt, Blome, Brack, and Hoven unlawfully, willfully, and knowingly committed war crimes, as defined by Article II of Control Council Law No. 10, in that they were principals in, accessories to, ordered, abetted, took a consenting part in, and were connected with plans and enterprises involving the execution of the so-called “euthanasia” program of the German Reich in the course of which the defendants herein murdered hundreds of thousands of human beings, including nationals of German-occupied countries. This program involved the systematic and secret execution of the aged, insane, incurably ill, of deformed children, and other persons, by gas, lethal injections, and diverse other means in nursing homes, hospitals, and asylums. Such persons were regarded as “useless eaters” and a burden to the German war machine. The relatives of these victims were informed that they died from natural causes, such as heart failure. German doctors involved in the “euthanasia” program were also sent to Eastern occupied countries to assist in the mass extermination of Jews.
Now, this “euthanasia” part is just the extreme. We see SIGNS of this, like Cuomo and his health people deliberately infecting nursing homes, but we are not realizing that much of the DAY-TO-DAY COVID CRAP is actually quite NAZI.
HERE is a lady, still alive who remembers ALL of what we are seeing now, happening under the Nazis. (Hat Tip to Singingsoul for finding this for me. I had remembered seeing videos of her before, but had forgotten her name.)
Just listen to her. She looks at COVID COMMIES, and she sees COVID NAZIS.
Are you starting to see how bad of a situation we are in?
I need to talk about why – if you don’t want to be like me – you don’t want the jab.
The Clot Shot
What I’m going to show you here is REMARKABLE.
On the bright side, this Twitter thread EXPLAINS my China Virus case PERFECTLY. It explains every aspect of my cardiovascular and pulmonary symptoms. But why? It’s not about the virus – it’s about the vaccine.
Yes. Even though it’s about the VACCINE, it’s about the SPIKE PROTEIN – the CLOT PROTEIN – something that my case and the CLOT SHOT have in common.
But on the bad side – yeah. It’s VERY bad health news for a lot of us.
But on the good/bad side, it’s enough to send ANYBODY who advocates mandatory vaccination to a TRIBUNAL followed by PRISON or EXECUTION.
Seriously. THIS NEWS is all the justification needed for ANY non-Nazi portion of our military to begin arresting the COVID NAZIS who are pushing vaccination mandates, if they don’t STOP.
Vaccine mandates must stop immediately.
We need to LEARN from failure – NOT keep pushing it.
Time to explain.
Hang onto your testicles. It’s a hell of a trip.
(1) Pfizer vaccine causes HUGE (5-6X) reduction in the most important antibodies, while jacking up the “addiction antibodies” which FAIL on the next variant (are you starting to see how the addiction works?)
(2) EVERY recipient of the Pfizer vaccine is excreting the remnants of PEG in urine, most likely from the “pegylated graphene oxide” trade secret (molecular razor blades, absolutely unreal they used this shit).
(3) The “clot shot” isn’t just some recipients – it turns out that tests shows clotting is happening in MOST people getting the spike protein vaccines. They’re not BIG clots that are easily spotted – they’re small clots that need testing to show up.
(4) This is the clinical effect of the clots from the vaccines, and it is IDENTICAL to what the disease did to me. It causes lung damage not visible on X-rays, and that damage stresses the heart by pulmonary hypertension. The good news from my own experience is that PULMONARY VASODILATORS (like magnesium) are VERY HELPFUL.
(5) More boosters = more clots = more damage = faster death. The vaccines MUST be stopped. If Pfizer wants to redeem itself (remember – Nuremberg II), it needs to STOP VACCINE PRODUCTION and FIND PULMONARY ANTIHYPERTENSIVES AND VASODILATORS.
(6) Here you see the worsening with the third booster. I predicted this – ask people on this blog. I told people – DO NOT GET THE THIRD SHOT. That is where this goes fentanyl-level and you’re not gonna last. Anybody who keeps pushing vaccines and mandates, and that includes SECDEF, needs to be ARRESTED, knowing what we know now.
The chief epidemiologist in Iceland was CORRECT when he said we have to transition to NATURAL HERD IMMUNITY. Yes – he was CORRECT, until the LYING PRESS browbeat him into the INSANITY NARRATIVE.
He was RIGHT before he was “corrected by the socialist media” – which happens to science all the time now.
We have to catch it early, treat it, survive it, and have great immunity.
1/ Stunning news from Iceland – among the world’s most vaccinated countries – today.
Facing a huge new #Covid outbreak that translates into ~100,000 new US cases a day, the country’s chief epidemiologist now says natural infection is the only way to reach herd immunity… pic.twitter.com/eMEnJxkWYk
2/ And he is not going to propose more lockdowns or widespread boosters. They do want to vaccinate teens but they are getting pushback. From an Icelandic reader (as you can see, the articles back him).
What is so stunning about this is that a couple of weeks ago, as cases began to rise, Iceland looked to be going the opposite way and imposing a new wave of restrictions in the hope of bolstering vaccine effectiveness. Clearly they've recognized that strategy is impossible.
So why did the Iceland epidemiologist walk it back?
That takes us to our next two items.
Why are CDC and its Pawns Always Wrong or Lying?
Beyond the fact that Rochelle Walensky is a Tony Fauci crony from WAY BACK, there is something terribly wrong with CDC.
In my opinion, it is politicized to the point where it obeys some weird agenda that it either does not itself understand, or that it does understand and NUREMBERG II is needed.
Just listen to this front line doctor, who is trained in respiratory viruses and immunology, explain how the agency repeatedly contradicts what is KNOWN and LONG-ESTABLISHED SCIENCE about treating and vaccinating against viral infections. He does NOT mince words. He sees CDC lying, just like I do.
Go to 14:55 to hear him begin, after the initial 15 minutes of the meeting (video MAY start there).
Let me put it this way.
It is important to follow the SCIENCE of PRACTICED MEDICINE and NOT the POLITICS of CDC, or the STOCK VALUE of PFIZER.
This is exactly what I found when “global warming” was forced on the entire scientific community. The “authorities” were repeatedly WRONG, but were never removed from authority for their errors.
Politics does NOT make science work. Politics DESTROYS SCIENCE.
Now – here is where the media comes in.
The Media’s Responsibility
What we have seen is the opposite of the way the media used to function when it was healthy.
The media used to ask tough questions of EVERYBODY – their OWN questions – NOT questions to support today’s talking points of ONE PARTY.
The media was not so obviously driven by AGENDA. The MEDIA did not tell scientists what to think – especially politically preferred science that was either failing or wrong to begin with. The media followed the SCIENCE – and the SCIENCE followed the TRUTH by painful argument and contradictions of its own beliefs.
SCIENCE fought and MEDIA reported.
SCIENCE worked and MEDIA reported.
The media is different now.
The media:
pushes a narrative that is repeatedly WRONG
does not want to pursue certain truths
hounds politicians, experts, authorities, and others who don’t offer approved viewpoints
seems to serve corporate and leftist political interests
The media will have much to answer for, if it KEEPS PUSHING MANDATES for MURDEROUS VACCINES.
So – where does this all go?
Conclusion: Keep It Up, and It’s WAR.
Pushing these vaccines any further is CAUSE FOR WAR for the American People. It’s that simple.
The insane left in America has been fed a real line by RevCom, with their “Bash a Fash” Antifa nonsense, farmed out to leftist youth, and aimed quite absurdly at the normal Americans who overwhelmingly chose Donald Trump against off-the-charts cheating.
The stark TRUTH is that American Bolsheviks of all stripes are pushing and pushing a DYING BRAND, and with the help of this damnable Maoist virus, they have created MEDICAL NAZISM, pushed by a LEFTIST controlled media, and supported by corporate globalists who don’t give a rat’s ass about patients – only about political power, profits, and CONTROL.
It’s one thing to pump a drug like Remdesivir that was basically a loser, but could have been regarded as a “hope-builder” of sorts.
It essentially does nothing but get cash for its makers, but at least it does no harm.
Original Investigation Infectious Diseases
July 15, 2021
Association of Remdesivir Treatment With Survival and Length of Hospital Stay Among US Veterans Hospitalized With COVID-19
Michael E. Ohl, MD, MSPH1,2; Donald R. Miller, ScD3,4; Brian C. Lund, PharmD1; et alTakaaki Kobayashi, MD1,2; Kelly Richardson Miell, PhD1; Brice F. Beck, MA1; Bruce Alexander, PharmD1; Kristina Crothers, MD5,6; Mary S. Vaughan Sarrazin, PhD1,2
Question: Is remdesivir treatment associated with improved survival or shortened hospitalizations among people with COVID-19 in routine care settings?
Findings: In this cohort study of 2344 US veterans hospitalized with COVID-19, remdesivir therapy was not associated with improved 30-day survival but was associated with a significant increase in median time to hospital discharge.
Meaning: The findings suggest that routine use of remdesivir may be associated with increased use of hospital beds but not with improvements in survival.
Abstract
Importance Randomized clinical trials have yielded conflicting results about the effects of remdesivir therapy on survival and length of hospital stay among people with COVID-19.
NOT SO THIS SNAKE-VENOM VACCINE
In my opinion, it is MURDER to try to make anybody take this vaccine involuntarily.
But it gets worse.
Pushing the vaccines drives the China Virus to new levels of pathogenicity. We have been warned repeatedly about this – even by an advisor to Bill Gates’ own pet organization CEPI – and yet it’s full steam ahead.
This is literally unconscionable. It’s not just murder – it’s MASS MURDER.
This is not acceptable.
So I am warning all proponents of mandatory vaccination.
You are headed to literal war, and from there, to only one place.
Nuremberg II.
Please reconsider before it’s too late.
Millions of Americans are ready to do the right thing. AGAIN.
*And One Study Showing How Much of a SCAM Fauci’s Beloved Remdesivir Actually Was
The old wisdom of science and medicine, from when I was a kid, has never been disproved. Stated simply:
Disease-conferred immunity in the recovered is always superior to any form of vaccination.
This is why, when we were kids, most scientists and doctors were “unimpressed” by the idea of moving to vaccines for the three main childhood diseases, which diseases themselves provide LIFELONG IMMUNITY against three illnesses that are MUCH ROUGHER on adults.
Why go to a lesser immunity? The diseases are mild in children. The outcomes are excellent. The immunity is SOLID.
Now you can push around the edges of this generality, and find examples where individuals DON’T get good immunity from a “first case” of a disease, and catch it again, whereas some other person gets life-long immunity from a vaccine. Nonetheless, the generality holds at the statistical level, and has always held, because it is LOGICAL.
The whole point of vaccination is to provoke a SUFFICIENT DEFENSE by a LESSER ASSAULT than the disease being prevented.
Thus, for the generality of the old wisdom to be violated, logic, math, and basic biology have to be overturned.
Which is not hard with Democrat minds.
Democrats want to believe things that are politically expedient but simply untrue. I wish I could say the same accusation cannot be leveled against our side, but I can’t. Nevertheless, I find that I can gently correct our side with actual scientific logic, whereas the other side demands “authority”, which they instantly deny to any person or organization that disagrees with them. It’s a solid defense, but it’s not a REAL defense.
In any case, communism is “politics as religion”, and thus it can lead to articles of hope and faith that are held in violation of common sense and widely agreed simple facts – even the most basic science that can be proven at home by anybody.
Thus, the much more solid and honest wisdom of 1960s and 1970s medicine and science began to disappear as the Soviets and Maoists began chipping away at it. By now, it’s in real trouble.
With the COVID hoax, I pretty much thought science was done for. Surprisingly, in the wake of the hoax’s general failure to convince EVERYBODY that up is down and vice versa, we are seeing more and more of the sheepish scientists and doctors who initially went along with things, turning around and disagreeing – although very gently – with the COVID madness.
I would like to show you SIX important points that are now known from scientific studies. You will not see the Bidenistas and Bidenazis trumpeting any of these.
What these points do, is basically show why we don’t need COVID vaccines, nor a particular bad drug called remdesivir.
Indeed, in my opinion, all of these things call into question the entire COVID response, and appear to make it some kind of scam – likely by the World Economic Forum.
I believe that the scam is for global population control, the latter meaning both control of people and control of reproduction.
I’ll explain that at the end, but a bit along the way, too.
PS – thanks to Wheatie for the above image, to RF121 for the link to 4 of these papers, and to Wheatie again for information about the Rockefeller Foundation censoring “misinformation” through Red Jen and Actor Vivek.
Six Points, To The Point
1 – Disease-conferred immunity appears to be 6.72 TIMES as strong as immunity from the COVID vaccines
2 – mRNA vaccines cause spike protein to begin circulating in the bloodstream almost immediately
3 – The antibodies raised by COVID vaccines show pre-existing “memory” immunity to COVID and the vaccines
4 – 99% of those infected by C19 show fast, specific, and effective (“robust”) antibody response
5 – For 2-shot vaccines, shot 1 needlessly elicits memory antibodies, but shot 2 dangerously elicits prompt antibodies
6 – Remdesivir does NOT work against COVID, but it does lengthen time in the hospital
OK, people. Let me break down THOSE items with fuller descriptions.
Six Points, Explained
1 – Disease-conferred immunity appears to be 6.72 TIMES as strong as immunity from the COVID vaccines
Yeah, gotta love those insignificant digits. SEVEN WILL DO – roughly.
This is from an Israeli study that looked at all the people getting infected right now. You will recall that almost all Israelis are vaccinated, yet all of a sudden, people are getting it again – which means that most of them have to be (and in fact WERE) vaccinated.
It turns out that, among the people who are getting COVID in Israel right now, are a few people who had it already – but VERY few of them. If you do the numbers, then it’s clear that catching the disease provides better protection than the vaccine. This is hardly unexpected – like I said – this was old school predictable knowledge back in the 1960s and 1970s.
Stated differently: “Catch a cold one year, you probably won’t catch it again next year, or the year after.”
COMMON. WISDOM.
The number may be a quibble – earlier estimates were actually HIGHER than a factor of 7. So this is a conservative estimate.
But let me repeat what I said. This is exactly what we expect from colds and flu bugs. EXACTLY.
Bottom line, they tried to take something that we already knew, and repackage it as something new and scary. Now, it’s easy to see that this was all about keeping and gaining power over us.
2 – mRNA vaccines cause spike protein to begin circulating in the bloodstream almost immediately
This is actually one of FOUR papers cited in a frontline doctor organizational email, which was then explained in the now-famous video by Dr. Sucharit Bhakdi.
If you have NOT seen this video, you should watch it. If you have seen it, then what you will be reading here (the next 4 points) is what he’s talking about, but related more directly to each of the 4 papers.
The email that describes the 4 papers will be included as an appendix. It describes the significance of the 4 papers, but I am restating that significance in my own terms, here, from my own perspective.
In my opinion, this first point shows exactly why the mRNA vaccines are so problematic, and were never a good idea. Not only is there a ton of vaccine migration PROVEN by the Pfizer leaked documents – there is massive spike protein circulation in the bloodstream. This spike protein activity circulating throughout the body is clearly the cause of all the problems associated with the vaccine.
In my opinion, it’s not a mistake. I believe the manipulated purpose of the vaccines was in fact incremental population reduction by flushing very early pregnancies on a huge but statistically significant scale.
3 – The antibodies raised by COVID vaccines show pre-existing “memory” immunity to COVID and the vaccines
This is a SMOKING GUN. What this means is that all the health authorities LIED to us about a lack of pre-existing immunity. The vaccines are immunizing people to something they are already somewhat or even completely immune to.
Read that again. “Asymptomatic cases” = “basically already almost completely immune”.
Remember early in 2020, when a lone, old, distinguished professor of immunology in Europe dared to publish online a STATEMENT (no way could he get it into a journal) that only pre-existing immunity could explain what we were seeing clinically with COVID-19, and his letter was then censored everywhere?
He is proven COMPLETELY RIGHT in this paper.
Now that we can carefully study new infections with COVID-19, it turns out that people are responding to the disease as “something they’ve seen before”. Yes – it’s THAT similar to the other weak beta coronaviruses.
As many have said, the disease was not actually novel. It was JUST NOVEL ENOUGH. Just novel enough, thanks to gain of function, to win the race for the seasonal best-seller. It’s like a new paperback romance that breaks no new ground as either literature or love-porn, but simply puts tiny tweaks on something everybody has seen before.
Fifty Shades of Nonfluenza.
I repeat. This was a WEAPONIZED COLD – a “new” cold – and THEY KNEW IT.
This was an ECONOMIC ASSAULT on the world. And likely by the World Economic Forum.
Which incidentally sponsored Event 201.
You FUCKERS.
4 – 99% of those infected by C19 show fast, specific, and effective (“robust”) antibody response
The point here was that EVERYBODY who gets COVID-19 – including those who barely have any symptoms or NONE AT ALL – get excellent antibody response – and they SHOW IT. The antibodies may go away, leaving the strong and effective MEMORY antibodies on standby, but the system is soon primed and ready to go.
Which then raises the question – in combination with the prior points…..
Wouldn’t most healthy people just want to get the DISEASE instead of the vaccine? They get better immunity, proven, even if they have ZERO symptoms.
We were SNOOKERED.
This goes back to something that the Fake News media and Fake Medicine CDC hid from us.
When antibody tests first became available, there was an apparent hesitation by authorities (particularly in blue states) to release results. HOWEVER, there were several “blooper” releases of information from hospitals and doctors – at least one of which was forced into disavowing their own prior statement.
What they were finding was double-digit numbers of people who already had antibodies to COVID-19. At that point, the antibody tests were SUPPOSED TO BE unique for COVID-19, and NOT for the prior beta coronaviruses. But yet, they showed antibodies for 30% of people or HIGHER. Later, authorities (including CDC) badmouthed the antibody tests as being flawed because they were picking up antibodies to “other coronaviruses”.
NOW it is completely possible to see what they were trying not to admit. Between prior exposure to both COVID-19 itself and strains of the other 4 weak beta coronaviruses, people were ALREADY IMMUNE.
OLD ANTIBODIES WORKED ON COVID-19.
You see what I’m saying? They would rather falsely “admit” that the tests were “not working”, than to truly admit that the tests worked TOO WELL, and most of us were already immune to COVID-19 to varying degrees. Why? Because that would eliminate the FEAR.
They reframed the PROTECTIVE cross-strain immunity as a test problem, rather than a natural immunity blessing.
It was all about the election. It was all about government control.
It was all a LIE and a HOAX.
5 – For 2-shot vaccines, shot 1 needlessly elicits memory antibodies, but shot 2 dangerously elicits prompt antibodies
This part is actually rather interesting. This is a point that Dr. Bhakdi makes late in his video. The first vaccine shot is NEEDLESS but HARMLESS. Well – more or less. Most people are actually IMMUNE TO THE VACCINE.
Yeah, I want you to read that again.
They can reframe reality – I WILL REFRAME IT BACK.
When you inject somebody with a needless vaccine to which they are already immune, the people simply have an immune response to the assault. Yeah, you can call it a booster, or whatever, but the point is that you have caused the immune memory to replay an old tape and pump out antibodies that work IN GENERAL on your new COVID strain. Vaccine. Whatever.
But the second injection, coming shortly thereafter, is potentially WORSE than NEEDLESS. With two injections, the first kicks up fresh antibodies to spike protein. The second infects YOUR cells and makes them a target of those antibodies.
This is why we saw all those people DIE after their second injection.
THEY. DID. NOT. NEED. THAT. SECOND. INJECTION.
Yeah, this will be a good fight in science – AND the courtroom.
Frankly, I think there need to be lawsuits here, for anybody who would have had a normal contraindication to a second shot, which IMO should have been ALL diabetics, cardiovascular patients, etc. In fact, many of those folks should not have gotten a first shot, because IMO the people that COVID didn’t kill in spring of 2020 were mostly immune, INCLUDING diabetics.
They didn’t need the vaccine. And the vaccine – especially the second shot – killed them.
And hey! If it had been ok to criticize vaccines earlier on social media and not get kicked off, we might have discovered this earlier, and saved a few lives! And dollars!
But no, we live in a fully Orwellian world, where Polish pink diaper that censors people telling the truth about vaccines gets AWARDS for protecting free speech.
6 – Remdesivir does NOT work against COVID, but it does lengthen time in the hospital
This is just “sweet revenge” as Ted Nugent called it. KARMA.
Now I have to admit that I was just as fooled as Trump on this. Fauci – what a scammer.
I saw in the very earliest results that remdesivir was WORSE than not working – it was removing people’s kidneys faster than COVID was. AYE-YI-YI. Bad stuff.
And yet Fauci had the BRASS ASS to go on national television and call remdesivir the “GOLD STANDARD” after that performance. Sheesh! Trust me – Trump saw it, too. This was CLASSIC “you have to show them”.
Admittedly, to some extent, this was “fighting the fear”, and you can see why the POTUS has to take part. But who was generating the fear?
Yeah. Much easier to see the controlling characteristics of the hoax NOW.
Anyway, scientifically, the problem is, there is no point in giving people an antiviral like remdesivir AFTER the virus has already created devastation. You have to deliver the antiviral EARLY – exactly like Dr. Zelenko realized very early on.
Doesn’t matter what KIND of an antiviral – even a piss-poor one, or an atypical one, like hydroxychloroquine, is going to WORK if it gets there EARLY. Late – it simply doesn’t matter.
Now the thing is, remdesivir has to be INJECTED. It could only be used in a HOSPITAL setting – or at least, so they said. I disagreed. People inject stuff in SUBWAYS. Let’s get SMART here.
Well, as a CHUMP HONEST SCIENTIST, my thought was, why not simply administer remdesivir early, by injection, at a lower and safer dose, on an outpatient basis, upon diagnosis? In the doctor’s office, or at a specialist. Nothing worse than a blood draw. Same time that people are being given hydroxychloroquine, or regeneron. It would actually WORK then.
WELL, you see, this paper does more than just prove that remdesivir doesn’t work. I proves WHY they never did the logical thing with it.
Administer it early and effectively, and you don’t SELL AS MUCH. Administer it late and desperately, and you sell a TON of it. And it’s expensive as HELL.
Oh. My. God. I was such a chump. I assumed they would do the right thing if they knew what that was.
The pharmaceutical industry, at this point, is CRAVEN. THEY JUST SELL PRODUCT.
Y’all remember how Fauci bullshitted Trump about remdesivir – how he lied about moving the goal posts? Helps if you know the full story about it, but here’s new evidence that the shit’s actually harmful.
In my opinion, it is now time to call this crap out.
This is one of the most needless vaccines ever – one of the worst outcomes for a vaccine ever – no matter which one – and it is BECAUSE COVID-19 is fundamentally a case where there should not BE a vaccine for most people.
This is a case that was KNOWN not to be very amenable to a vaccine. It was only by a FEAR PSYCHOLOGY OPERATION that we were scammed into accepting the idea that we needed a really badly performing COLD VACCINE.
It’s a MONEYMAKER for industry – their PAWN MOTIVE – and a CONTROL AGENT for various levels of government – their PAWN MOTIVE. Ultimately, it’s about a global effort to gain control – most likely being mediated through the World Economic Forum, since almost all the guilty parties are either “partners” like Google/Alphabet or “organizations” like the Rockefeller Foundation.
And THAT is where we find the really basic motivation for the COVID hoax – as a PLATFORM of human control.
Once I realized that Bill Gates created Windows not as an operating system, but as a PLATFORM to change human behavior into a path he created, I realized the power of creating PLATFORMS. It’s a GOD THING.
You see, the mandatory vaccine platform is basically “The Island” where the entire planet is “The Island”. The people in control are liars, they can inject you with whatever they want, and they then have power of life and death over you, because they lie with impunity.
To start with, I believe the globalist scum are introducing a kind of limited, very incremental contraceptive.
TL;DR – you MUST listen to a short podcast of a scientist revealing the latest research on the spike protein vaccines. The VACCINE ITSELF (not just the spike protein – the mRNA vaccine itself) is persistent and is not only concentrating in ovaries – THE VACCINE ITSELF IS EXCRETED – e.g., in breast milk. Meaning …
“When the people have any power to object to a socialist solution, a deniable 5% fait accompli is always more desirable to socialists than a negotiated 50% solution, because they can always negotiate on the remaining 95%.” -Wolf Moon When I first heard about a case of a miscarriage by a pregnant doctor, due to …
Using Principles of Protein Equivalence and Analogy as Predictive Tools for Coronavirus Understanding Surely you’ve heard of the BROWN RECLUSE SPIDER. The brown recluse is related to several other recluses, and a couple of other families of spiders, that all have a similar venom – a protein called sphingomyelinase D. This is an enzyme that …
Now – if you followed that patent history work that Dr. David “Bowtie” Martin did on the coronavirus and vaccines, then you realize that they’ve been aware of the spike protein for TWENTY YEARS. Its CONTRACEPTIVE activities had to have been known – likely from before understanding of the spike protein per se, when coronaviruses were just viruses which caused potentially contraceptive symptoms in some patients.
This is a no-brainer, people. We have been manipulated.
W
John Fink and James Coburn discuss case in a scene from the film ‘The Carey Treatment’, 1972. (Photo by Metro-Goldwyn-Mayer/Getty Images)
Appendix: The Letter
Letter to Physicians: Four New Scientific Discoveries Regarding the Safety and Efficacy of COVID-19 Vaccines
SCIENTISTS CONCLUDE THE BENEFIT OF COVID-19 VACCINATION IS “HIGHLY DOUBTFUL” BUT VACCINE INJURY IS “WELL SUBSTANTIATED”
Doctors for Covid Ethics has sent the following letter to tens of thousands of doctors in Europe, summarising four recent scientific findings critical to the COVID-19 vaccination program. The letter explains each finding as it relates to the biology of COVID-19 vaccines, including interactions with the immune system.
Taken together, the letter warns that these new pieces of evidence force all physicians administering COVID-19 vaccines to re-evaluate the merits of COVID-19 vaccination, in the interests of their own ethical standing, and their patients’ safety and health.
A video explanation of the underlying immunology by Professor Sucharit Bhakdi MD is here, with German subtitles here.
*
Dear Colleague:
Four recent scientific discoveries are herewith brought to your urgent attention. They alter the entire landscape of the COVID-19 pandemic, and they force us to reassess the merits of vaccination against SARS-CoV-2.
Summary
Rapid and efficient memory-type immune responses occur reliably in virtually all unvaccinated individuals who are exposed to SARS-CoV-2. The effectiveness of further boosting the immune response through vaccination is therefore highly doubtful. Vaccination may instead aggravate disease through antibody-dependent enhancement (ADE).
Discovery 1: SARS-CoV-2 spike protein circulates shortly after vaccination
SARS-CoV-2 proteins were measured in longitudinal plasma samples collected from 13 participants who received two doses of Moderna mRNA-1273 vaccine [1]. With 11 of the 13, the SARS-CoV-2 spike protein was detected in the blood within only one day after the first vaccine injection.
Significance. Spike protein molecules were produced within cells that are in contact with the bloodstream—mostly endothelial cells—and released into the circulation. This means that a) the immune system will attack those endothelial cells, and b) the circulating spike protein molecules will activate thrombocytes. Both effects will promote blood clotting. This explains the many clotting-related adverse events—stroke, heart attack, venous thrombosis—that are being reported after vaccination.
Discovery 2: Rapid, memory-type antibody response after vaccination
Several studies have demonstrated that circulating SARS-CoV-2-specific IgG and IgA antibodies became detectable within 1-2 weeks after application of mRNA vaccines [1–3].
Significance. Rapid production of IgG and IgA always indicates a secondary, memory-type response that is elicited through re-stimulation of pre-existing immune cells. Primary immune responses to novel antigens take longer to evolve and initially produce IgM antibodies, which is then followed by the isotype switch to IgG and IgA.
A certain amount of IgM was indeed detected alongside IgG and IgA in some studies [1,4]. Importantly, however, IgG rose faster than IgM [4], which confirms that the early IgG response was indeed of the memory type. This memory response indicates pre-existing, cross-reactive immunity due to previous infection with ordinary respiratory human coronavirus strains. The delayed IgM response most likely represents a primary response to novel epitopes which are specific to SARS-CoV-2.
Memory-type responses have also been documented with respect to T-cell-mediated immunity [5–7]. Overall, these findings indicate that our immune system efficiently recognizes SARS-CoV-2 as “known” even on first contact. Severe cases of the disease thus cannot be ascribed to lacking immunity. Instead, severe cases might very well be caused or aggravated by pre-existing immunity through antibody-dependent enhancement (ADE, see below).
Serum antibody profiles were reported for 203 individuals following SARS-CoV-2 infection [8]. 202 (>99%) of the participants exhibited SARS-CoV-2 specific antibodies. With 193 individuals (95%), these antibodies prevented SARS-CoV-2 infection in cell culture and also inhibited binding of the spike protein to the ACE2 receptor. Furthermore, CD8+ T-cell responses specific for SARS-CoV-2 were clear and quantifiable in 95 of 106 (90%) HLA-A2-positive individuals.
Significance. This study confirms the above assertion that the immune response to initial contact with SARS-CoV-2 is of the memory type. In addition, it shows that this reaction occurs with almost all individuals, and particularly also with those who experience no manifest clinical symptoms.
The goal of the vaccination is to stimulate production of antibodies to SARS-CoV-2, but we now know that such antibodies can and will be rapidly generated by everyone upon the slightest viral challenge, even without vaccination.
Severe lung infections always take many days to develop, which means that if the antibodies generated by the memory response are needed, they will arrive on time. Therefore, vaccination is unlikely to provide significant benefit with respect to the prevention of severe lung infection.
Discovery 4: Rapid increase of spike protein antibodies after the second injection of mRNA vaccines
IgG and IgA antibody titres were monitored before vaccination and after the first and the second injection of mRNA vaccines [3]. Antibody titres rose with some delay after the first injection, then plateaued, but rose again very shortly after the second injection.
Significance. Even though the antibody response to the first injection is of the memory type, the small time lag after the injection may mitigate adverse reactions, because the abundance of spike protein on the cells in the blood vessel walls and in other tissues may have already passed its peak when the antibodies arrive.
The situation changes dramatically with the second injection. Then the spikes are produced and protrude into the bloodstream that is already swarming with both reactive lymphocytes and antibodies. The antibodies will cause the complement system [9,10] and also neutrophil granulocytes to attack the spike protein-bearing cells. The possible consequences of all-out self-attack by the immune system are frightening.
Antibody-dependent enhancement of disease
As described, memory-type immune responses ensure the rapid rise of antibody titres after initial exposure to SARS-CoV-2, rendering the benefit of vaccine-induced antibody response exceedingly doubtful. Regardless, we should not assume that high antibody titres against SARS-CoV-2 will always improve the clinical outcome. With several virus families—in particular with Dengue virus, but also with coronaviruses—antibodies can aggravate rather than mitigate disease. This occurs because certain cells of the immune system take up antibody-tagged microbes and destroy them. If a virus particle to which antibodies have bound is taken up by such a cell, but it then manages to evade destruction, it may instead start to multiply within the cell. Overall, the antibody will then have enhanced the replication of the virus. Clinically, this antibody-dependent enhancement (ADE) can cause a hyperinflammatory response (a “cytokine storm”) that will amplify the damage to the lungs, liver and other organs of our body.
Attempts to develop vaccines to the original SARS virus, which is closely related to SARS-CoV-2, repeatedly failed due to ADE. The vaccines did induce antibodies, but when the vaccinated animals were subsequently infected with the virus, they became more ill than the unvaccinated controls (see e.g. [11]). The possibility of ADE was not adequately addressed in the clinical trials on any of the COVID-19 vaccines. It is therefore prudent to avoid the danger of inducing ADE through vaccination and instead rely on proven forms of treatment [12] for dealing with clinically severe COVID-19 disease.
Conclusion
The collective findings discussed above clearly show that the benefits of vaccination are highly doubtful. In contrast, the harm the vaccines do is very well substantiated, with more than 15.000 vaccination-associated deaths now documented in the EU drug adverse events database (EudraVigilance), and over 7.000 more deaths within the UK and the US [13].
ALL PHYSICIANS MUST RECONSIDER THE ETHICAL ISSUES SURROUNDING COVID-19 VACCINATION.
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Notes
1. Ogata, A.F. et al. (2021) Circulating SARS-CoV-2 Vaccine Antigen Detected in the Plasma of mRNA-1273 Vaccine Recipients. Clin. Infect. Dis. -:x-x
2. Amanat, F. et al. (2021) SARS-CoV-2 mRNA vaccination induces functionally diverse antibodies to NTD, RBD and S2. Cell -:x-x
3. Wisnewski, A.V. et al. (2021) Human IgG and IgA responses to COVID-19 mRNA vaccines. PLoS One 16:e0249499
4. Qu, J. et al. (2020) Profile of Immunoglobulin G and IgM Antibodies Against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). Clin. Infect. Dis. 71:2255-2258
5. Le Bert, N. et al. (2020) SARS-CoV-2-specific T cell immunity in cases of COVID-19 and SARS, and uninfected controls. Nature 584:457-462
6. Grifoni, A. et al. (2020) Targets of T Cell Responses to SARS-CoV-2 Coronavirus in Humans with COVID-19 Disease and Unexposed Individuals. Cell 181:1489-1501.e15
7. Gallais, F. et al. (2021) Intrafamilial Exposure to SARS-CoV-2 Associated with Cellular Immune Response without Seroconversion. Emerg. Infect. Dis. 27:x-x
8. Nielsen, S.S. et al. (2021) SARS-CoV-2 elicits robust adaptive immune responses regardless of disease severity. EBioMedicine 68:103410
9. Magro, C.M. et al. (2020) Docked severe acute respiratory syndrome coronavirus 2 proteins within the cutaneous and subcutaneous microvasculature and their role in the pathogenesis of severe coronavirus disease 2019. Hum. Pathol. 106:106-116
10. Magro, C.M. et al. (2021) Severe COVID-19: A multifaceted viral vasculopathy syndrome. Annals of diagnostic pathology 50:151645
11. Tseng, C. et al. (2012) Immunization with SARS coronavirus vaccines leads to pulmonary immunopathology on challenge with the SARS virus. PLoS One 7:e35421
12. McCullough, P.A. et al. (2021) Pathophysiological Basis and Rationale for Early Outpatient Treatment of SARS-CoV-2 (COVID-19) Infection. Am. J. Med. 134:16-22
13. Johnson, L. (2021) Official Vaccine Injury and Fatality Data: EU, UK and US.
This is for the historical record. I hope that this analysis gets to the “dissident scientists” involved, but even if it never does, future historians will get a powerful look at what I call “Fake Science” – the establishment’s phony, deceptive and controlled scientific complex – and how infiltration, control, and discreditation of dissident populist …
You will recall that I located the point where the “suramin error” was dropped in front of the right people to be uploaded to the prominent doctors of the anti-vaxx community, prior to the “magnet challenge” disinformation being similarly uploaded, and then used to discredit them in the Daily Mail.
Part of the suramin attack involved a highly edited video of Judy Mikovits touting suramin, minus the full information about that drug. That video, in combination with erroneous assertions about suramin being in pine tree needles, resulted in the physicians who are currently prominent warning about the COVID vaccines, picking up the error and discrediting themselves in their very current and very popular videos about the gynecological and shedding problems of the persistent and migratory spike protein vaccines.
Well, that video which was used to misinform them has been removed.
Sunlight. It cures quite a bit all on its own.
More seriously, I realized that, at some level there, probably in the background, I was dealing with pro “influencers of influencers of influencers”. I won’t be sharing all my information on that, as much as I would love to, but it became apparent that they are watching us like hawks. Speaking of which…..
2.
The Sleeper Has Awakened
Yes, Sundance just came out with a piece critical of the COVID vaccines. You will recall that SD and his crew were all fairly pro-vaxx, so this tells me there is a fundamental shift going on.
And while the fact that the HHS entrance to VAERS went down at the same time SD came out with this article may very well just be coincidence, I am 100% certain that the policy of Barack Obama and Eric Holder is BACK IN PLACE under Merrick “Whatever You Say, Barack” Garland, and that journalists like Sundance (and ourselves) are being SPIED ON by the federal government, in a abuse of power for political purposes.
SO – anyway – keep an eye on CTH in regard to things “COVID” – there is going to be some good stuff there, I’m willing to bet.
[Just for the record, I wrote this BEFORE the recent CTH post about “QAnon” stuff, which I happen to regard as a very helpful warning, but which was “not received warmly” by most on this site. I’m not looking to exacerbate the situation, but I hate “spiking” anything – for anybody. And I’m going to be very blunt. Sundance is going to have THE BEST coverage of DOJ asshattery against our site, so prepare to see me using a LOT of his coverage in my postings and reasoning. People need to learn to keep their emotions in check, because that is how an army survives – digital or otherwise. WWG1WGA begins with YOU.]
3.
Scientists Are Calling Out The Snakes
Everybody is seeing how people are calling out FAUCI, but in my opinion that’s actually a side-show. The REAL DEAL is scientists calling out the scientific BULLSHIT about COVID, and particularly the spike protein nuttery that was imposed on us. At long last, people in Scienceville are going “WHAT THE #### IS GOING ON?”
First, a video that came to us via Grandmaintexas and this link:
It’s worth listening to the beginning of this video to hear this dude list off his credentials. This guy isn’t just some country doctor. Nor is he old, senile, or out-of-date on current medicine. Just listen to him. This dude is IMPRESSIVE. He’s still sharp as a tack, just like Trump. I would almost say “more”, at the risk of offending some who believe this is not possible! Just listen to him.
Among many other jaw-droppers of sensible scientific perspective, this video basically tells you why I have been so mouth-agape about that Pfizer data snagged back into American science from JAPAN.
You have to look closely at it, but not THAT closely.
The VIDEO adds more about testicular localization in males.
Yeah, boys. It ain’t just the broads. Cross those legs – this is gonna make you cringe like a prostate exam.
One of the things which is EXTREMELY NOTEWORTHY about the video is that this lady YouTuber / Facebooker / BitChuter and all-around “social media presenter” goes into deep detail about the extreme censorship she is encountering, and how she deals with it.
For example, she states that the YouTube video was taken down in about 10 minutes.
Alternatively, you can listen to some different scientists in THIS great video, thanks to singingsoul.
Here we have Bret Weinstein interviewing a doctor and an engineer who explain – to the satisfaction of any honest scientist – WHY the mRNA vaccines (and to a lesser extent, the adenoviral vector vaccines) are CLEARLY problematic.
This is EXACTLY the same stuff we’ve been talking about. And it will be extremely useful in getting to where we are going, looking at NEW VACCINES COMING.
I’ll give you a hint now – the new vaccines could be a strong correction, back to what vaccines SHOULD be – or they could just be a slower and stealthier path to get us where the cabal has us going now – elite-controlled social contraception, and immunity debt enslavement – which is the worst-case future of “vaccine capture” a la Marek.
So – let me review previous posting, mostly mine, but also Deplorable Patriot’s reachy but prophetic question about the incredible and previously unthinkable idea of vaccine shedding. All of it based on what YOU, our loyal posters, brought here for the group to digest.
Take a bow, people. YOU DID GOOD.
4.
A Short Bibliographic Toldjaso From This Site
I will preface each of these blurbs with another short blurb, explaining relevance.
This will “refresh your memory”, before we get into the FUTURE.
We start, very appropriately, with RAND PAUL.
Gotta give DOCTOR Rand Paul credit – he has led the fight to bring SANITY back to medicine and science. Thank GOD Trump put him where he saved the most people – in the SENATE. I also have a personal debt here, as a recoveree, forced to wear a needless mask, aggravating my hypoxia. Rand Paul has FREED ME of my TORTURE MASK.
Introduction You have GOT to see the video I’m going to show you. It’s not just what they’re talking about. It’s WHERE IT LEADS. Most of the people who watch Rand Paul go after Fauci here, are concentrating on MASKS, because that is the TOP LAYER of the argument. But THAT is the small potatoes. …
This post is where disparate cracks in the narrative all opened at once. I was no longer going along with the bullshit. Too many questions, too many pat answers turning up WRONG – no – the narrative was full of holes, and it was time to think ON OUR OWN.
PREFACE I thought that I might withhold this post on Easter Sunday, and then I changed my mind, thanks to Deplorable Patriot, Trump, Gab and Jesus. If anybody ever FOUGHT on Easter Sunday, it was Christ. It’s time to FOLLOW POINT. The Branch Covidians have taken a toll, but the WAR is turning, and – …
I just went back and read this thing, and – WOW – just WOW. I was all over two things – spike protein and genetic incorporation – the JAENISCH paper. We are now all over the spike protein, but we MUST turn our attention to genetic incorporation of the vaccine – particularly in people who “fountain” the spike protein. I had forgotten this, but much of the suspicion of Fauci on this site centered around his seeming obsession with vaccines for viruses capable of genomic incorporation.
Yes, Wuhan is important, but I see that as the plotters playing “hot potato scandal” to distract us from the deeper purposes of this LYING phony pandemic.
Genetic incorporation of these vaccines must be investigated. There has been so much we have been told that is WRONG – I think genetic incorporation due to the spike protein acting as a reverse transcription promoter for its own RNA is a biggie.
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 …
No good guys among these genetic vaccines. They are all RISKY for certain people, and when we EUAed them forward, we took those risks. The problem is, with idiot BIDEN in charge, instead of Trump, there was nobody to push the sensible idea of sparing the vaccine from those for whom it would be knowingly risky.
Every coronavirus vaccine so far has shown us SOME defect upon mass release, which was NOT evident in EVEN phase III clinical trials. Look HERE for a searchable PDF document of adverse effects from the Pfizer vaccine: https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/977005/COVID-19_mRNA_Pfizer-_BioNTech_Vaccine_Analysis_Print.pdf Check out these videos on the low-platelet clotting problem from the Oxford/Astrazeneca vaccine. Here is a fantastic …
I was really starting to get it here. I was starting to accept that “it’s the full spike protein, stupid!”
I saw an excellent explanation of the clotting problem with the AstraZeneca vaccine against SARS-CoV-2 / COVID-19 here: The doctor, Dr. ZDogg, MD, offers an exceptionally clear explanation of both what is going on with the AstraZeneca vaccine, and why its distribution was halted or limited in some places for some age groups of patients. …
This is when I realized that all the gynecological problems being reported for the COVID vaccines were actually a REAL problem, and not just a sub-problem of the clotting problems. I also realized that this effect was too pronounced to be an accident. And then the complications going to other people in close contact – how could this even be possible?
So I considered what sounded like a more reasonable alternative to “vaccine shedding” – namely, spike protein shedding. Indeed, both avenues could be operating, but vaccine shedding now has DATA to support it, in the form of the Pfizer animal data showing persistence and migration. And if you stay with this to the very end, you will see that these lipid nanoparticles have been nothing but trouble from the beginning. It’s an impressive technology, but clearly not fully baked.
Thus, read this post, knowing that the vaccine is likely to be nearly as persistent as the spike protein it produces. Everything I’m saying for the spike protein, should apply in spades for the vaccine, which essentially brings in mRNA as a transmissible FACTORY for creating spike protein. It would not take much vaccine transfer to create the EXACT problem that is observed in alleged shedding incidents.
“When the people have any power to object to a socialist solution, a deniable 5% fait accompli is always more desirable to socialists than a negotiated 50% solution, because they can always negotiate on the remaining 95%.” -Wolf Moon When I first heard about a case of a miscarriage by a pregnant doctor, due to …
This is where I really laid out the evidence that the spike protein is causing the problems we’re seeing.
Using Principles of Protein Equivalence and Analogy as Predictive Tools for Coronavirus Understanding Surely you’ve heard of the BROWN RECLUSE SPIDER. The brown recluse is related to several other recluses, and a couple of other families of spiders, that all have a similar venom – a protein called sphingomyelinase D. This is an enzyme that …
If you don’t think those “lipid nanoparticles” of the mRNA vaccines can’t “act like viruses” and basically pass “disease” to a NEW HOST – read this. LNPs ≈ VLPs.
EVERYTHING we are seeing in vaccine medicine now is a COPY of what nature did about 70-100 million years ago, in the insect world. Once I realized this, I was able to pattern this stuff all over what Big Pharma is doing, and get ahead of their game.
This post is probably going to go over a lot of heads, but I think scientists will find it disturbing until they find it compelling, and then ultimately find it satisfying. Creation teaches us – not the other way around.
OK – we’re going to have some fun here – but stick with me, and you could learn A LOT. Cue the music! Borrowed from Wheatie! Previous posts helped put both the SPIKE PROTEIN DISEASE and the SPIKE PROTEIN VACCINE into deep perspective. We were seeing that the SOLUTION was a significant part of the …
Deplorable Patriot hit the nail on the head here. Before I accepted the awful fact that these vaccines are not what we thought they were, I didn’t believe shedding could be real. Oh, boy, was I wrong about that.
Our dear boss, Wolf, has been busy putting together scientific primers on just what it is the various shots and inoculations marketed to be preventative of severe symptoms of COVID do, but what hasn’t been addressed for those of us who chose not to be shot up with whatever is in the syringes is how …
This was beautiful – mainstream science and medicine starting to question the Fauci BS. Revel in it. Some of this is now “accepted” – all of it will be, soon enough. We’re headed back to sanity, folks.
This is a very important video you don’t want to miss. It just came out, and the doctor is a guy I’ve been following. He chooses his words carefully, to stay inside the establishment where he can publish some of the top papers, but he speaks the truth at all times. Don’t let the video …
This is where I was blown away by the Pfizer leak out of Japan. The targeting of the ovaries.
AYE-YI-YI. What is one supposed to think? Good GRIEF.
TL;DR – you MUST listen to a short podcast of a scientist revealing the latest research on the spike protein vaccines. The VACCINE ITSELF (not just the spike protein – the mRNA vaccine itself) is persistent and is not only concentrating in ovaries – THE VACCINE ITSELF IS EXCRETED – e.g., in breast milk. Meaning …
Now you can see it very easily – the enemy threw that “Magnet Challenge” out to muddy the water as we were gaining understanding. But here is where I started to look at it experimentally – give it a real examination – and come away fairly doubtful that there is anything to it. The Magnet Challenge is bad science. It may be well-motivated, but it’s quality disinformation. Top-shelf stuff – ACTIVE DISINFORMATION to make people SELF-DISCREDIT – meant to insulate the controlled and groomed experts by discrediting smart people outside of controlled science.
Wherein we examine, in something like “MythBusters” style, the dubious “Magnet Challenge”, without relying (too much) on the anti-scientific crutch of scientific authority First, a confession. The main reason I am attracted to these videos of people sticking magnets to the COVID vaccination injection sites on their shoulders, is that I love to watch normal …
This is where I actually call out the other side for trying to mislead our side with the “Magnet Challenge”. At this point I really understand how utterly misleading this trick is, and WHY it was inflicted on us.
Wherein we look at how the COVID scammers are now using “magnetic” disinformation to try to escape justice for REAL abuse of liposome biotechnology to achieve [most likely contraceptive] vaccine persistence and migration. TL;DR – after mRNA vaccine persistence and anatomical migration were revealed in leaked Pfizer data, explaining “shedding” via persistent liposomes, the COVID …
This is where I investigate the origins of one of the “fake facts” used to trip up the doctors opposed to the spike protein mRNA vaccines. I am convinced that this was some kind of discreditation operation – a precursor to the “Magnet Challenge” psy-op.
This is for the historical record. I hope that this analysis gets to the “dissident scientists” involved, but even if it never does, future historians will get a powerful look at what I call “Fake Science” – the establishment’s phony, deceptive and controlled scientific complex – and how infiltration, control, and discreditation of dissident populist …
At this point, you should be ready for more information – about WHERE vaccination is going.
5.
New Vaccines – The Great Crony Blame Escape
It took me a while to put 2 and 2 together, but when I first saw the June 7 cover article on my new “vaccine snitch”, Chemical & Engineering News, something bothered me about it.
This is more excellent reporting by Ryan Cross, who routinely ferrets out (pun intended) the full story on virus science and vaccine technology, as available to “public science” – to be distinguished from the deeply hidden stuff. Cross never adds in any politics, crime, depolitical deconstruction, “conspiracy theory” speculation, or any of the things that are MY JOB. I have to respect that. This is the way THE NEWS used to be.
get the facts
understand the facts
teach the facts
teach the understanding
light fuse, run away
AH. I love my job. BE THE FUSE.
Figuring out the criminality of the government, industry, and financial backers – getting past the obscurantism, deceptions, and lies – that is OUR JOB – We The People – for we are (now that Merrick Garland soils the DOJ with Chicago communism) the
REAL DEPARTMENT OF JUSTICE.
Yup. WE are not the communist insurrection and their corporate cronies, destroying everything in their path to money and power, including honest science and doctor-patient medicine.
We are (and like Confucius, I WANT them to hate this) the RESURRECTION.
The RESURRECTION vs. The INSURRECTION.
Eat your own label, insurrectionist commies. It’s good for you!
OK, back to science.
I really encourage you all to read this full article, which is written so that the general public can understand 99% of it easily. You will learn a LOT about vaccine technology. I will move you along through it, skipping over things, but when we’re done, consider reading the whole thing both WITH and FOR greater understanding.
I will try to only quote selectively from it, as I capture a few key points. But I can do no better than to give C&EN’s own “TL;DR” which they label “In brief“:
Vaccines are synonymous with shots, but it doesn’t have to be that way. More than a dozen groups are working on COVID-19 vaccines that can be squirted or sprayed into the nose instead of injected in the arm. Besides the potential practical advantage of easier administration, these vaccines could trigger the mucosal immune system to make antibodies in the nose and help stop the coronavirus at its point of entry. It sounds great, but the mucosal immune system is hard to study, and pharma companies have been reluctant to invest in the needle-free approach. Mucosal immunologists and intranasal vaccine developers are hoping the pandemic will change that.
This is where my first “2+2” $0.02 comes in.
Note the final statement:
Mucosal immunologists and intranasal vaccine developers are hoping the pandemic will change that.
It’s not the phony pandemic that is “going to” change delivery route. It’s already happening, in my opinion, due to the massive unveiling of not just the problems of the systemic gene therapy vaccines, but the clear motivations behind these vaccines, some of which were not just hidden from the public, but also from the scientific community, which I believe is now getting WISE.
Stated more simply, OUR PRESSURE in getting out the TRUTH about the existing vaccines is forcing the industry to react to vaccine shortcomings they WILL NOT ADMIT otherwise. The industry is likely also under forces from ABOVE THEM which are also being exposed.
You will see this as I go through the article.
The most powerful weapons in our hands are the UNDERSTANDINGS of the following:
spike protein toxicity
vaccine persistence
vaccine migration
spike genetic incorporation
Fauci’s reverse transcription obsession
Bill Gates’ “pre-programming the experts”
Zuckerberg connection to Baric lab
irrational hatred of cheap available therapeutics
generality of therapeutics being fought, thus…
the enabling of ChiCom manipulations
ovarian and testicular targeting
hiding of evolutionary knowledge
“circuits of plausibility” to create errors and crises
Put these things together and the “easy path” of systemic vaccines which do NOT mimic stimulation of natural immunity as well as NASAL VACCINES do, has been chosen under the cover of simplicity, but in reality because it always lies closer to what the industry TRULY wants, e.g., right now, gene therapies, where they NEED to target many specific organs. Nasal vaccination is a niche safety point which has always WAITED while systemic gets the action the deep backers want and NEED.
When it’s just easier and possible to do the wrong thing they want, they DO IT.
The current gene therapy desideratum – organ specificity – is actually in another article in the same issue of C&EN, talking about CRISPR, anti-CRISPR, and how to make gene therapy not have side effects, a point which is admitted more openly now that they are “safe on first” by having “proven” that gene therapy “works”.
Such a scam.
But it gets worse. Industry motives are not the motives of those who manipulate THEM.
As you read the rest of this, note that the “running dog” industry layer, which now performs for taskmaster commies, is also manipulated by THEIR true masters, the global elite, now looking at pesticides for humans, and particularly deplorables. It’s clear to me now, after the ovarian, placental, and testicular actions of the spike protein broke media containment, that the reason the entire vaccine industry jumped into full spike protein gene therapy tests masquerading as necessary vaccines is manipulation by the one guy who double-controls vaccine technology via “owning” CEPI – and that would be BILL GATES.
Yes, that Bill Gates, whose father is standing behind Fauci here.
Thus, when both the Gates Foundation and CEPI back some project, it’s Bill Gates getting TWO SCOOPS of control.
Note also Event 201 backing.
With Fauci and the Faucists inside government, and Bill Gates on the outside, there was no way that safer, metered, recombinant spike protein tech or peptide subunit tech was ever going to go first. They needed the new tech given a carte blanche, and they got it. This plus the “crisis” allowed the full spike protein’s foot to be shoved in America’s door, past everybody who might have questioned it.
This is one of the guys who spotted the “snake protein analogy” first, in what would have been time to alter the landscape.
No longer random, this is what happens when people get in the way of a conspiracy TWO LEVELS UP, where the really big boys and girls play. There are money motivations in between, but this guy’s real crime was potentially interfering with “the spike must flow”.
Have I raised your suspicions?
GOOD! Let’s look more deeply at the article now.
In fact, the mucosal membranes that line our airways, digestive systems, and reproductive tracts are often the first parts of our bodies to face an invading pathogen. A network of immune cells resides underneath our mucous membranes, or mucosae, and forms a front line of defense against invaders, and they prevent most infections from taking root. This is the mucosal immune system, and some immunologists think we have been seriously underestimating it.
“When you think about it, that’s where we acquire most of our infections: we inhale them, we consume them, or we get them through sex,” says Michael W. Russell, a mucosal immunologist and professor emeritus at the University at Buffalo.
This is where we begin to realize that mucosal immunity and systemic immunity are NOT the same thing. And it doesn’t have to be “either/or” – you can have BOTH. There are many plausible reasons for one over the other, but it will become clear that using the mucosal pathway adheres more strongly to the natural “API” of immunity by “contact”, if you will, with the pathogen, rather than sudden systemic introduction.
Have we really been underestimating it? Or have we been IGNORING IT ON PURPOSE at the highest motivational levels of power?
In my opinion, if the powers that be in VAXX WORLD would have been looking out for us all this time, there would have been stronger forces pushing researchers toward mucosal immunity. The problem is, that kind of naturalistic and patient-centered thinking is a problem for those who see vaccination as more of a path to power or other ends, particularly SOCIAL ends, rather than as part of a path to individual health. Nothing has made this more clear than the “pandemic”, controlled by “experts” who seemed not to know what they were doing.
Are you now starting to understand how and why conspiracies are intentionally mischaracterized as giant joint illicit cooperation, when they are in fact TOWERS OF LAYERS OF INTERNAL DECEPTIONS?
Good. Let’s move on.
Our mucosal immune cells make a special class of antibodies that are constantly secreted from the mucous membranes to protect the nose, gut, and other vulnerable sites from pathogens we’ve seen in the past. “But if you don’t stimulate the immune system in the mucosae, you don’t obtain mucosal immune responses,” says Pierre Charneau, head of the Molecular Virology and Vaccinology Unit at the Pasteur Institute.
Yet most research on SARS-CoV-2 and our immune systems has overlooked mucosal immunity in favor of the easier-to-study systemic immunity. “When the pandemic hit last year and I started to see papers coming out about immunity, it really quite staggered me to see an absence of attention to the mucosal immune response,” Russell says.
See that? The TILT of the field – the RUSH to systemic – that is a SOCIAL phenomenon – and socialists, or believers in the effectiveness of socialist tactics, like me – will tell you very honestly that science can be controlled SOCIALLY – that the SOCIAL aspects of science are not all warm campfires around each other’s blogs, but actually PART OF THE FIGHT that controls WHAT SCIENCE THINKS and WHAT SCIENCE DOES.
Or like this blog. I’m just honest about it.
I keep telling people that the “jabs” were PUSHED and SHAPED to be what they were – for REASONS – diverse yet all valid – which compromised all the insiders to DO WHAT WAS NEEDED to create what was needed at the TOP:
SYSTEMICALLY MOBILE, GONAD-TARGETING, SPIKE PROTEIN OVERDOSE INJECTIONS AT CONTRACEPTIVE LEVELS.
Stated more generally, it wasn’t a BUG – it was a FEATURE. And we were RUSHED into testing (if not USING) the feature ON PURPOSE.
Now – remember how COVER works – these vaccines did what they were SUPPOSED to do in our little world – but they also did what other people wanted in THEIR little and very exclusive world of “human benefactors”.
We move on.
Charneau and a group of scientists in Paris have shown that natural SARS-CoV-2 infections trigger both systemic and mucosal immunity. But our current crop of COVID-19 vaccines offer only systemic protection. Developing vaccines that are sprayed up the nose, rather than injected into the arm, could change that, Charneau says. Mucosal immunity in our noses could be like a guard at the door, potentially helping stop even small infections of SARS-CoV-2 right where they start.
It’s a tantalizing notion, but whether it’s a viable one is up for debate.
Now, the FIRST thing I think when I read this is “hey, that means my disease immunity is almost certainly BETTER than vaccine immunity – as doctors have all known for decades prior to COVID-19”.
Of course, we know they lied about that to “prevent vaccine hesitancy”. Or stated using different words, “to prevent picking the mild disease over the vaccine in the safer age groups, the latter being most of them”.
Do you see that? Almost ANY lie can be justified in the name of “overcoming vaccine hesitancy”. Who, besides Fauci and CDC is so obsessed with that Swiss army knife excuse and viral talking point?
But you know what – Fauci knew this – and Rand Paul knew Fauci knew this. So when Rand Paul went after Fauci on reinfection of COVID recoverees, like both HIM and ME, he knew Fauci was on THIN ICE.
But toss that all aside. At BEST, we went straight after systemic immunity “because emergency”. But it turned out that it wasn’t all that big of an emergency, and that’s where it gets interesting.
As I said, things are changing very rapidly now – obviously getting a technology on the cover of Chemical & Engineering News is a big deal.
And I quote:
After all, the pandemic provided a chance for messenger RNA (mRNA) vaccine technology to finally prove its worth, and mucosal immunologists are hoping that this will be a moment for intranasal vaccines to do the same. “This climate is a game changer,” says Hiroshi Kiyono, codirector of the University of California San Diego Center for Mucosal Immunology, Allergy, and Vaccines. “This is a great opportunity to advance nasal vaccines, not just for COVID-19 but for other respiratory diseases.”
YUP. That’s the way CRISIS MECHANICS works. The “crisis” is just going to CHANGE, to get people to do a NEXT NEW WRONG THING.
My advice to Hiroshi Kiyono would be WATCH OUT – you are going to be subjected to many pressures that bring mucosal vaccines TOWARD viability as spike protein contraceptives. There will be pressure AWAY FROM doing what is best for the PATIENT, and TOWARD doing what is best for the SCIENCE and the RESEARCH, and that “better” will just happen to be better for surreptitious social or even sociobiological manipulations, too.
This is just a HEADS UP.
I’ve been there. Fake Science is not a very nice place to be when billions or trillions of dollars are on the line, and YOU’RE IN THE WAY.
At this point, the article goes into the HISTORY of intranasal vaccines, intranasal being one of the very best routes for respiratory virus vaccines. I’m going to SKIP over all that, even though there are some very interesting aspects to that history. I don’t really see any smoking guns of obstruction or sabotage, but it’s pretty clear that intranasal was a bit of a black sheep, and fended for itself.
Now, HERE is what’s interesting. Which intranasal vaccines are “in the pipeline”?
TURN YOUR NOSE UP
More than a dozen intranasal vaccines are in development for COVID-19. Here are several to keep an eye on.
Phase 1
Altimmune ▸ Adenoviral vector
AstraZeneca and University of Oxford ▸ Adenoviral vector
Beijing Wantai Biological Pharmacy, University of Hong Kong, and Xiamen University ▸ Live attenuated influenza virus vector
Bharat Biotech and Washington University in St. Louis ▸ Adenoviral vector
Codagenix and Serum Institute of India ▸ Live attenuated SARS-CoV-2
Laboratorio Avi-Mex and Icahn School of Medicine at Mount Sinai ▸ Live Newcastle disease virus vector
Meissa Vaccines ▸ Live attenuated respiratory syncytial virus vector
Preclinical
AuraVax and University of Houston ▸ Recombinant spike protein with adjuvant
HanaVax and University of Tokyo ▸ Recombinant spike protein with adjuvant
TheraVectys and Pasteur Institute ▸ Lentiviral vector
University of Eastern Finland and University of Helsinki ▸ Adenoviral vector
Sources: Companies, World Health Organization.
Now, that may not look like much, but there is a TON to unpack, because we not only have OLD “new” technologies in a NEW route – we have NEW “new” technologies to explain – and in a new route.
If you don’t think the other side can cause trouble with their spike protein attack through the nose, you are sorely underestimating the ability of those who CONTROL SCIENCE to “get there first” and mislead the rest of the pack.
Remember – if you think like me, then you know people have been doing this crap for billions of years in THIS universe alone. We’re just “rediscovering reality under supervision” on one more planet. The lies are OLD. Very, very OLD. And as I like to say, “Satan weaponizes everything.”
The adenoviral vectors we’ve seen. That’s AstraZeneca, Johnson+Johnson, Sputnik V, and others. The only difference is that they’re going through the nose, where these viruses are actually supposed to go.
There is a LOT of possibility that this move could solve the biggest problems with these vaccines. IF the nasal delivery route is a kind of highly evolved and intelligent natural “attenuation gauntlet” for viruses, then the outcomes for these vaccines could be uniformly improved.
IF that is indeed the case, then I’m going to be a “toldjaso” asshole and use this as part of my explanation of why “they” have divided us in the specific way they have, over the topic of evolution, separating the “intelligence” side from the “evolutionary science” side, thus pushing the latter to view evolution as DUMB instead of “cautiously and obsessively path-checking”, which looks dumb to localized intelligence that doesn’t know how to keep its biases in its own lane.
These vaccines also introduce lentiviral vectors – pretty much the same thing as the adenoviral vectors, just a different virus. Again, this is new, so it could be interesting.
Another returning technology is Recombinant spike protein with adjuvant. That is basically Novavax, which we have not really had a chance to deconstruct, because there is not yet much public information on safety or efficacy. So a big QUESTION MARK on that one. In principle this should be safer than genetic technologies, both because there are ZERO risks of genomic incorporation (see Jaenisch for SARS-CoV-2 incorporation), and because there are no possibilities of unmetered “fountaining” of spike protein.
First up in technologies we have NOT seen yet: Live attenuated SARS-CoV-2.
We have already used INACTIVATED SARS-CoV-2 – that would include the Chinese Sinovac vaccine, which is rebranded as CoronaVac in the West. I’ve been cautioning that I believe “bad lots” of CoronaVac, which are incompletely inactivated, have been passed off, which would explain why there is typically a surge in cases right when countries start using CoronaVac. Obviously that’s good for business, and we know how Chinese business works. The only other explanation would be that PCR is picking up vaccine during rollout, and I’m half-way thinking that’s a better explanation, were I not so familiar with ChiComs and the corruption they spread.
However, we have NOT yet seen live attenuated virus. This could be GREAT – or it could have a whole NEW bag of problems. I’m very “wait and see” on this.
The real BIGGIES of the new intranasal vaccines are these:
Live attenuated influenza virus vector
Live Newcastle disease virus vector
Live attenuated respiratory syncytial virus vector
Unlike the adenoviral vector vaccines, which are basically “working but dead mRNA in a dead skin suit of a different virus that’s easy to work with”, these vectors are LIVE VIRUSES with “something extra” (like the spike protein) inserted into their genes, making them chimeric at the genetic level, not just the vector level.
These vaccine viruses are actually designed to “run a bit”. They INFECT YOU with instructions to crank out spike protein.
This is where things start getting weird, and it’s hard to trust a world which contains both THIS technology AND the CCP.
You know what I’m sayin’?
But now let’s look at all these. We suddenly have a LOT of vaccines to keep track of.
It’s gonna take some work – but we have to do it. We cannot let them keep experimenting on us like they did, while CHINA did almost NO “experimentation” on its people.
Understand what I’m sayin’?
Good.
Now – the rest of the article is basically the HOPES and the NOPES of the intranasal route. Some of the possibilities here are MIND-BOGGLINGLY GOOD.
Mucosal immune cells constantly make an antibody called secretory immunoglobulin A (IgA), which gets released into the mucous membranes of the nose, mouth, airways, and gut. Pound for pound, we produce more IgA than any other antibody, Russell says, although most of it is broken down and sneezed, coughed, or pooped out within a few days.
And critically, while injected vaccines induce only systemic immunity, vaccines delivered to mucosal sites can induce both systemic and mucosal immunity, he says.
That fact is evident in animal studies of a vaccine being developed by David T. Curiel and Michael Diamond at Washington University in St. Louis. Both the injected and intranasal forms of their vaccine triggered the production of IgG antibodies, but only the intranasal route triggered mucosal immune cells to secrete IgA that blocked the virus from replicating in the nose. A day after they published preprint data demonstrating as much in July 2020, the Indian vaccine company Bharat Biotech contacted the university’s technology-transfer office to license the intranasal vaccine in India, where it is being tested in a clinical trial. “How that will play out clinically remains to be seen,” Curiel says. “But this animal model finding suggests, qualitatively, that we have some additional benefit.”
It is very clear that – for a respiratory disease – there is an advantage to having “naturally obtained” respiratory mucosal immunity.
All that said, we’re still talking spike protein. But if the intranasal route can keep it out of the ovaries, testicles, and placenta – GREAT.
And THAT brings me to another great C&EN report by Ryan Cross – everything you want to know and need to know about those damned lipid nanoparticles.
Without these lipid shells, there would be no mRNA vaccines for COVID-19
Fragile mRNA molecules used in COVID-19 vaccines can’t get into cells on their own. They owe their success to lipid nanoparticles that took decades to refine
Without doing any “gotcha” journalism, Cross reveals the GOOD, the BAD, and the UGLY about these lipid nanoparticles.
The impression I get is that this field was dogged with problems, most of which were overcome, but not all.
So, without getting into the details, all these criticisms of the lipid nanotech that you are hearing are NOT “conspiracy theories” – the scientists are TALKING ABOUT THEM as real problems they’re trying to solve, with various degrees of success, in this report.
To me, it was very clear that people WAY above these scientists needed to PUSH this LNP (lipid nanoparticle) technology, necessary for GENE THERAPY, into acceptance using the phony plague.
If you don’t want to take this stuff, STAND UP for your rights. Otherwise, it’s over the hill, the horses are OUT OF THE BARN, the fence is open and the cattle are GONE.
BUT – I think that if we keep pushing the REALITIES of these vaccines, we can make the “mandate martinets” crawl back into their Fuehrer Bunkers and leave us alone.
And THAT is worth it.
W
PSSSST – hey, DOJ and FBI. Want to see some audit results?
THEY’RE EXPLOSIVE!
Seriously, you injustice-perpetuating assholes deserve to be trolled. Your phony allegations of “violence” or even potential violence by the QAnon “believers” are an affront to Americans. They’re a SICKNESS coated with a patina of professionalism. You should be ashamed of yourselves.
