Making Sense of Pro-Vax Trump

Risks, Bets, Rewards and Losses – Why Vaccine-Conferred and Disease-Conferred Immunity are Both Proper Personal Gambles When Choice is Free and Enough Truth is Known or Unknown


Many of us were shocked that President Trump just showed his “pro-vax” hand in an interview with vaxx nutt Bill O’Reilly, but if you watch Trump long enough, you realize that he very often gets to the optimal perspective before anybody else – even with incomplete data.

https://twitter.com/disclosetv/status/1472987776786354177

It’s worth wondering why Trump said what he said, and said it when he said it.

Beyond the “credit” issue – which I can really see for many reasons, not the least of which is because Trump’s plan really messed up the Cabal plans on COVID – I think Trump knows people who are seeing the emerging data. And I think they are advising him correctly.

I’m going to try to show you some of that data, and what it means.

Rand Paul is a sharp guy, too. Trump respects Rand Paul. It pays to ask why. I think that part of it is because Rand is a doctor. Trump respects doctors, I am convinced. And Trump knows that doctors differ in their opinions, like everybody else, and that he (Trump) needs to listen to a number of them, to see where the best perspective resides.

Rand is not anti-vaxx. He’s pro-natural-immunity. There is a difference.

At the place where Trump’s viewpoint and Rand Paul’s viewpoint intersect, you will find much truth. I certainly did. And when I added in a few other doctors “on our side”, and looked carefully at where I was skeptical of some of their thinking, but also let them convince me to be skeptical of some of my own thinking, I hit the jackpot.

BOTH the vaccines AND the disease make sense as alternative, risky, immunity-conferring antigens. Neither one is obviously superior to the other for everybody, because the landscape of risk and benefit is too complex, and depends far too much on the needs, goals, and medical circumstances of the individual. Worse still, past choices – including accidental ones – affect future choices.

Rand Paul saw right into this – that the CRUX of the problem is that “natural immunity” is being ignored by a monetarily, scientifically, and institutionally compromised medical establishment. Natural, disease-conferred immunity is the BEST CHOICE for many people – particularly when combined with a “delay of onset” strategy, and TREATMENT, which alters the risk/benefit. We have known this all along, yet we have never truly internalized it, because the “Let’s You And Him Fight” strategy of the OBAMA MANDATES has widened and deepened the division between those who choose vaccines and those who don’t.

AND LOGIC.

Trump GETS THIS. And he said so. We ARE falling into their trap. BUT we can turn that around on a DIME.

It is critical for our side – the free and sane medicine side – to EXPOSE and BASH the performance of the vaccines, because the other side won’t do it. But it is also critical that we STAND UP for the freedom for others to take those risky vaccines voluntarily, and accept the truth that it can make sense, during a period where we don’t know everything, and MAYBE beyond that, after we know more.

Mandates are absolutely stupid, reckless, and anti-science. They interfere with medicine. The mandating commies need to BTFO. But letting fearful people take a risky vaccine – a personal gamble – is a part of freedom that we have to respect.

I want to show you data that makes this make sense.


Some of you may be surprised that I am defending the COVID vaccines AT ALL. At present I have ZERO intention of taking one. For me, and my wife, they are a BAD medical choice. For many others, too.

Well, what if I tell you that in doing so, I can defend disease-conferred immunity EVEN MORE?

What if I tell you that I can now see why, strategically, Trump waited until we “knee-capped” – but didn’t kill – the vaccines?

BOTH SIDES HAD TO SEE MORE CLEARLY.

Let me help you see more clearly.


Natural Immunity – More Risk With More Reward?

What I just said there is not always true.

For CHILDREN, it appears that the vaccines are MORE RISK, LESS REWARD.

Yeah, Trump was right about that.

It’s a NO-BRAINER to NOT, NOT, NEVER, EVER give this shit to kids, and I personally hope that God himself does whatever is needed to save children from the MONSTERS who are injecting them with these RELATIVELY dangerous vaccines.

Kids are being deprived of EXCELLENT natural immunity, for JUNK immunity that makes money for Big Pharma.

Just for starters, we may be condemning these kids to a lifetime of life-robbing spike boosters, just by virtue of a well-understood idea of “original antigenic sin”, or OAS. OAS is where one antigen leads to an inappropriate response to a later antigen, vaccine, or infection.

This means that if we give children a misleading FIRST ANTIGENIC STIMULUS, they may then be STUCK with sub-optimal antibody immunity, leaving them for an unknown time at GREATER RISK from the disease. It may very well be that the BEST FIRST ANTIGEN for SARS-CoV-2 is the DISEASE – not a spike protein vaccine.

We don’t KNOW what will happen long-term when we inject kids. Or, at least, most of us don’t. Maybe Fauci does.

OLYMPUS DIGITAL CAMERA

Is it a good idea? Should we bet ALL our kids on that idea?

NO FREAKING WAY.

And THAT is assuming that these vaccines do nothing to affect fertility. If they DO affect fertility, then this has to be made a KNOWN and ADMITTED risk, at the very least – not covered up, like it is right now.

A call for Nuremberg II, more likely, if this was knowingly advanced.

Who wants to risk their kids’ chance of having children?

This brings up the question of whether parents have the right to *knowingly* neuter their kids. Some parents already are, by “transing” kids. I think it’s pretty clear that’s where the Cabal is going – neutering and spaying humans. Interesting question. Should it be sent to SCOFFLAW SCOTUS? How is Amy Comey Barren going to vote on that one?

Asking for a FIEND.

I would even extend that thinking to teens and young adults. There is no reason that I can see to give them the vaccine. But should they have that choice, in consultation with their doctors? Interesting question. Very hard to reconcile a pro-life position with that, isn’t it?

But back to natural immunity.


Natural Immunity – More Rewards

Are there, in fact, more rewards?

I think so. Look at these two figures from the UK Ministry of Health, showing spike protein antibodies in people in England in 2021.

LINK:

…..https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/1027511/Vaccine-surveillance-report-week-42.pdf

The darker the color, the stronger the antibodies.

The first graphs are people who have no evidence of having caught the disease (N protein negative). They include the unvaccinated uninfected and the vaccinated uninfected.

The yellow is the unvaccinated people who have not caught the disease – mostly kids.

Green, blue and purple are various levels of vaccination success – the darker, the more spike antibodies.

Now look at people who got some or all of their spike immunity by natural infection with the disease.

Assuming it’s a wash as far as the quality of the antibodies – which is not necessarily true – it’s obvious that these recoverees have a more robust spike antibody immunity – to say nothing of likely immunity to some or all of the other 20+ proteins in SARS-CoV-2.

Rand Paul, right here. The man is asking the right questions.

So why is Fauci ignoring this natural immunity stuff?

Notice that KIDS don’t mount a strong spike immunity, even though they beat down the disease in a hurry, with minimal symptoms. This is likely an EVOLVED RESPONSE – an EVOLVED STRATEGY – a form of EVOLVED INTELLIGENCE. What it says is that kids “know” by evolution – don’t build a lasting defense to the ever-changing spike protein. Meanwhile, the virus tries to “rope-a-dope” us slowly into concentrating on the spike as we age, misleading us with each attack. We lean on the crutch of spike antibodies that don’t work on the next strain, or actually make things worse.

Kinda funny that Fauci and the “follow the science” types don’t respect this signal from evolution, but whatever. That’s the basis of another post. But keep it in mind – it’s likely important.

So let us not digress.

The bottom line is that IF you’re going to make spike antibody immunity your standard of success, which Fauci and company clearly have, as part of Fauci’s “antibody hypnosis”, then by that standard, “natural immunity” from the disease gives MORE REWARD.

And again, I remind you, there are MANY other metrics of immunological success which are highly relevant, and which are ignored under Fauci spike antibody hypnosis. Always keep that in mind.


Natural Immunity – More Risks

SO – is the disease “more risk” to get that more reward?

My answer would be “maybe”.

It’s a complex calculation – particularly if you factor in “not getting the disease until you get it”. When you vaccinate, it’s a down payment in full, and with boosters, you’re even stuck with installments. You are “accepting that the risks happen” at 100%. Vaccination “collapses the probabilities”. But if you take your chances on the disease, by simply not vaccinating, you are delaying the (probably) higher risk, but the “risk over time” is substantially reduced.

Imagine the “payoff” of not vaccinating or getting the disease until Omicron. That would have been a GREAT gamble and winnings.

But let’s look at an ACTUAL COMPARATIVE RISK of vaccine vs. disease.

Now – let me be clear from the start – this article is a CLICK-BAIT CHERRY-PICKING of the highest order. The title numbers SEEM shocking – until you dig into it, and go to the source.

But still, they’re not “lying”. It’s just misguided. But that CHAFF led me to WHEAT.

Let me include the entire, short report, as it appeared in GWP.


On December 14th, 2021, Nature Medicine released a study based on a broad population data set analyzed by researchers at Oxford University. The researchers examined the risks of myocarditis, pericarditis, and cardiac arrhythmias associated with COVID-19 vaccination and infection.

The Oxford researchers reveal that 1 in 100 or 1% of all vaccinated individuals were admitted to the hospital or died with arrhythmia or irregular heartbeat.

Of the 38,615,491 vaccinated individuals included in our study, 385,508 (1.0%) were admitted to hospital with or died from cardiac arrhythmia at any time in the study period (either before or after vaccination); 86,754 (0.2%) of these occurred in the 1-28 days after any dose of vaccine. Of those who were admitted or died 39,897 (10.3%) had a SARS-CoV-2 positive test, with 29,694 (7.7%) having a positive test before vaccination. There were 7,795 deaths with cardiac arrhythmia recorded as the cause of death (1,108 had a SARS-CoV-2 positive test).

So 1 in 100 of the vaccinated individuals are going to the hospital with irregular heart beat and this isn’t international headlines?

This is a shocking number.

James Cintolo has more on this study.


Wolf again.

This study appeared in the journal NATURE. That is the big leagues. We have to take this seriously. But let’s look at it closely. It REALLY helps to see that entire document, although SUSPICIOUS CAT should come out, just looking at the TITLE.

NATURE PAPER: https://www.nature.com/articles/s41591-021-01630-0

Risks of myocarditis, pericarditis, and cardiac arrhythmias associated with COVID-19 vaccination or SARS-CoV-2 infection

See? This isn’t just about the vaccines – it looks at infection, too. Is Gateway Pundit giving us the full story? Maybe not.

ABSTRACT:

Although myocarditis and pericarditis were not observed as adverse events in coronavirus disease 2019 (COVID-19) vaccine trials, there have been numerous reports of suspected cases following vaccination in the general population. We undertook a self-controlled case series study of people aged 16 or older vaccinated for COVID-19 in England between 1 December 2020 and 24 August 2021 to investigate hospital admission or death from myocarditis, pericarditis and cardiac arrhythmias in the 1–28 days following adenovirus (ChAdOx1, n = 20,615,911) or messenger RNA-based (BNT162b2, n = 16,993,389; mRNA-1273, n = 1,006,191) vaccines or a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) positive test (n = 3,028,867). We found increased risks of myocarditis associated with the first dose of ChAdOx1 and BNT162b2 vaccines and the first and second doses of the mRNA-1273 vaccine over the 1–28 days postvaccination period, and after a SARS-CoV-2 positive test. We estimated an extra two (95% confidence interval (CI) 0, 3), one (95% CI 0, 2) and six (95% CI 2, 8) myocarditis events per 1 million people vaccinated with ChAdOx1, BNT162b2 and mRNA-1273, respectively, in the 28 days following a first dose and an extra ten (95% CI 7, 11) myocarditis events per 1 million vaccinated in the 28 days after a second dose of mRNA-1273. This compares with an extra 40 (95% CI 38, 41) myocarditis events per 1 million patients in the 28 days following a SARS-CoV-2 positive test. We also observed increased risks of pericarditis and cardiac arrhythmias following a positive SARS-CoV-2 test. Similar associations were not observed with any of the COVID-19 vaccines, apart from an increased risk of arrhythmia following a second dose of mRNA-1273. Subgroup analyses by age showed the increased risk of myocarditis associated with the two mRNA vaccines was present only in those younger than 40.

The TRUTH is right in there.

First, we have to remember that GWP was concentrating on 1% of vaccinated people during the study period, INCLUDING before they got vaccinated, going to the hospital for or dying from a cardiac arrhythmia. That “before they got vaccinated” point is a TIP, right there, that we really need to consider the risk for UNVACCINATED people, too – including these very same people – for comparison. And as an aside, what is the number for corresponding unvaccinated people? You can almost guess that for most old people, it’s gonna be – well – maybe 1%?

And indeed, when the researchers compared the risk of an “event” against the risks of these patients BEFORE vaccination, they got their answers.

The WORST CASE for the vaccines was myocarditis. So let’s look at that, first.

Here is the risk from the vaccines. Broken out with [notations] so it’s easy to understand.


We found increased risks of myocarditis

associated with the first dose of ChAdOx1 [AstraZeneca] and BNT162b2 [Pfizer] vaccines

and the first and second doses of the mRNA-1273 [Moderna] vaccine

over the 1–28 days postvaccination period,

and after a SARS-CoV-2 positive test. [STRONGLY NOTE THIS!!!]

We estimated an extra two (95% confidence interval (CI) 0, 3),

one (95% CI 0, 2)

and six (95% CI 2, 8)

myocarditis events per 1 million people vaccinated with ChAdOx1, BNT162b2 and mRNA-1273, respectively,

in the 28 days following a first dose

and an extra ten (95% CI 7, 11) myocarditis events per 1 million

vaccinated in the 28 days after a second dose of mRNA-1273.


SO – this confirms what we know. The vaccines cause myocarditis. It’s a RISK. It’s a handful or two in a million, per injection.

But now, let’s look at the NEXT LINE.


This compares with an extra 40 (95% CI 38, 41)

myocarditis events per 1 million patients

in the 28 days following a SARS-CoV-2 positive test.


What this says TO ME is that the risk of this one heart problem, in a vaccine that gives less immunity, is a significant fraction of the same risk from the disease.

Obviously due to the SPIKE PROTEIN, and possibly with a simple correlation to exposure.

I will admit that it’s LESS RISK from the vaccines, but not all that much.

Look at MODERNA.

The compiled risk of myocarditis from the TWO SHOTS (6+10 = 16) is 40% of the disease risk (40).

And yet HERE is how the authors have to word things to get it past the referees and editors.


“In summary, this population-based study quantifies for the first time the risk of several rare cardiac adverse events associated with three COVID-19 vaccines as well as SARS-CoV-2 infection. Vaccination for SARS-CoV-2 in adults was associated with a small increase in the risk of myocarditis within a week of receiving the first dose of both adenovirus and mRNA vaccines, and after the second dose of both mRNA vaccines. By contrast, SARS-CoV-2 infection was associated with a substantial increase in the risk of hospitalization or death from myocarditis, pericarditis and cardiac arrhythmia.


They played a lot of word games there – take it from a retired scientist. They are also STUDIOUSLY AVOIDING some big stories that would rub the industry wrong.

“Give the editors what they want.”

Now, before I examine that conclusion for further trickery on the “within a week” qualifier and several other points (not today), I just want to say that calling 16 “small” and 40 “substantial” is bullshit.

Author bias, implicit or imposed, as a virtue signal to Bill Gates’ “vaccine culture” in science.

I will bet MONEY that a third Moderna booster would come in at 14 or more, bringing the total myocarditis events from chronic spike protein exposure to 30 or more, AND at the 4th injection SURPASSING the risk of ONE untreated disease incidence.

Well, is it worth it?

I don’t want Dementia Joe telling ME that it’s worth it. I want to make that determination MYSELF.

And GUESS WHAT? I will also bet money that part of the reason that CDC wanted people to mix and match boosters was to get Moderna “recoverees” boosted with the less cardiotoxic Pfizer or J+J vaccines, while not admitting that…

….defects from each spike protein vaccine are cumulative.

See how that works? Science. It’s great when you’re HONEST.

And why IS Pfizer causing fewer cardiac problems? In my opinion, it is very likely because the vaccine is distributing more widely and slowly in the body, thanks to the extreme vaccine lipid nanoparticle longevity (hence shedding) and biodistribution – data that was hidden from us, but turned up in the Japanese freedom of information request.

To me, the fact that nobody sees or talks about this stuff, is just more evidence of “vaccine hypnosis” of academia, as noted by Peter McCullough.

The reality? PICK YOUR POISON. Disease or vaccine.

If we go back to the arrhythmia example, it turns out that the “shocking 1%” actually GOES AWAY when compared to the unvaccinated. This makes sense, when you recall the very common problem of “palpitation” sending people to the ER, long before “long COVID” was a thing.

Yeah, 1% is shocking, but it’s shocking for the unvaccinated, too. Gateway Pundit was just throwing unwarranted shade.

Now, let’s take a look at some GRAPHICS from the study. Pictures tell a thousand words – not all bad for the vaccines – not all bad for “natural immunity”.

On the left axis you have the three vaccines, AstraZeneca, Pfizer, and Moderna, followed by the disease.

On the bottom axis, time – repeated three times for the three diseases.

As you can see for cardiac arrhythmia (right side), the vaccines are basically fine, but the disease is problematic. This makes LOTS of sense, because the disease seems to cause many problems by nerve infiltration, secondary to vascular distribution, and those nervous system infections and inflammations are highly relevant for arrhythmias, whereas the vaccine is primarily a vascular villain, which does NOT reproduce and infiltrate.

The science makes sense here! Wonderful!

All of the vaccines have at least a little bit of myocarditis effect (left side), which is explained nicely by vascular distribution of the spike protein. Moderna, which is notorious for “disease-like symptoms” at the recipient experience level, is easily expected to have even more COVID-like spike protein effects that are not immediately obvious, such as myocarditis.

Big point – ONLY the disease (bottom side) kicks off all three diseases. THAT is what a virus can do, that a bare protein, or even a non-reproducing virus-like particle, cannot.

Everything is making sense here. Let’s look at ANOTHER view of the data.

This graph has some GREAT STUFF. The myocarditis comparison described in detail above, is the graph on the LEFT. The numbers for the vaccines look substantially less, but you can see how Moderna boosters would quickly approximate the disease, and are already like a “mild case” in terms of risks. The authors of the paper avoid talking about the cumulative risks, but it’s clear that “boosterama” is PRECISELY Fauci’s game plan, and it has problems that got solved for Moderna by mix-and-match boosters.

Fauci and Walensky. Always taking care of their companies. Yeah, I kinda get it. But you gotta be HARD-ASS with them, like Director Wolf Moon would be.

The whole vaccine thing – including a lot of other adverse effects I’ve mentioned previously but not discussed here – looks to me like a trade-off. These are NOT good vaccines. They’re actually pretty marginal. BUT for people who really don’t think they can take the disease, it could be a reasonable gamble, IMO.

There are LOTS of people who take these vaccines, and no problem. I know – I talk to them all the time. I’m the most vaccine-supportive vaccine skeptic on Earth. These people just dump everything to me, because they know I don’t judge them, but respect their decisions. I’m interested in what happened to them, and they tell me.

NADA. ZIP. The most common reaction. For those people, the shot may make sense. But there are a good number of others who get laid up hard for a day in bed, and it sounds almost as bad as COVID. I worry about them. Some – A LOT.

Now look at the second graph – myocarditis in younger people. Clearly Moderna is WAY out of whack, and the others are comparable to the disease when boosted. Again – for these people – really BAD vaccines. This is why you saw action on the vaccines. Get values up close to the disease, in terms of numerical risks, and the problem becomes an elevator pitch that everybody understands.

Pericarditis and arrhythmia? Purely a disease problem. This looks very good for the vaccine. This is what you WANT with a vaccine – to AVOID some problem of the disease. BUT – can we trust those numbers?

I think so, and I think that Gateway Pundit got burned by looking at COMMENTS on a blog post explaining the Nature study.

LINK: https://jamescintolo.substack.com/p/new-bombshell-myocarditis-study-out

This is a GREAT post – here is the conclusion:


 THE TAKEAWAY

Public health policy in the USA and UK need to change fast. As a side note, if you listen to the mainstream media enough they’ll have you believing myocarditis is a mild symptom. Let me be clear, by definition, symptoms requiring hospitalization are defined as severe. What’s more, the average mortality rate of non-fulminant myocarditis is nearly 56% which is experienced within 3-10 years. Sadly, that is a consequence of the likely heart failure that develops after the acute phase of myocarditis has resolved. See picture below 👇🏻

All things considered, it is clear that individuals under 40 are at a high risk of experiencing vaccine induced myocarditis. The good news is, there are ways to deal with this. More specifically, increasing the time between the first and second dose, not giving boosters to all healthy individuals under 40, pausing Moderna for many under 30, and seeking the guidance of other countries. All of that makes for better public health policy and positive health outcomes. To finish, I will leave you with the words of a wise man, “Health care is vital to all of us some of the time, but public health is vital to all of us all of the time”. – C. Everett Koop


Wolf again.

Now – in the comments, somebody mentioned the “1% issue”, and I suspect this is where GWP picked it up. Sadly, the comment author deleted and restated their comment, probably after realizing it had spawned a widely read article.

Here is the replacement comment, with replies.


zuFpM5*M6 hr ago I erased my previous comment. The closer I look at this study, the more it freaks me out.

They compare vaxxed to vaxxed+covid and then declare covid is worse, but they measure rates of myocarditis/pericarditis in post covid with troponin levels and in post vaxx with hospitalization rates. Hmmmm

They don’t include any control group of unvaxxed. The vaxx+covid group should be compared to unvaxx+covid to determine the actual rate of post covid heart issues. This is not done that I can tell?

The vaccinated showed a 1% hospitalization rate for cardiac arrhythmia with ~385,000 in the period up to 28 days post vaccination. I tried to look up population rates of hospitalization and found some old news articles discussing ~350,000-500,000 hospitalizations annually for ‘atrial fibrillation’ for the entire US population. So a group of vaccinated in UK blew out the entire US annual budget of arrhythmia hospitalizations in a couple month period? And that isn’t a highlighted part of the research results but instead they compare only within the vaccinated group broken out by short temporal periods? Isn’t the most important thing the vaccinated versus background normal rate?

I begin to think this whole study was gamed to get vaccinated rates of these issues versus supposed covid rates so they could continue to say vaccines are safer, when the actual #s are showing a horrific rise in these issues. It is a preemptive narrative shaping attempt.

I am not a doctor, researcher or number cruncher, so if I am misunderstanding this, I would be interested to hear how.
br143 hr ago There’s no way to sugar coat the study.

Of the ~385,000 people with arrhythmia, 10.3% had a positive Covid-19 test, and 7.7% tested positive at some point prior to vaccination.

Even if you remove 18% of the total, that’s still an awful lot of people with arrhythmia. I suppose most of us have some form of arrhythmia at some time in our lives, but how many of us are treated in hospital?
zuFpM5*M3 hr ago Yes. I would not subtract them either. I feel that there would be a covid risk increase + vaccine risk increase + covid/vaccine interaction risk increase to account for. None of which can be done without estimating the covid risk increase by comparing with non-vaccinated covid patients.

This is where they lost me. They’re just tossing out “maybes”. Nothing jumps out at me as likely to change the result. I can even add my own experience with cardiovascular issues from the disease. They’re REAL. Very unlikely that the vaccines and disease would FLIP on the relative risks of arrhythmia.

Score 1 for the vaccines.

BACK TO THE TRUMP ISSUE.


Benefits of the Vaccine Admitted by Our Side

There is a GREAT video by Geert Vanden Bossche that I keep pushing, because it is one of the clearest explanations of why “leaky mass vaccination” is a bad idea. Note that this is from a pro-vaxxer who has indeed worked with vaccines for his whole career, and is a former member of GAVI.

He just demands good vaccines, and good public vaccination policy.

Now – if you jump to around 4:30 in the video, you can hear him list the positives of the clot shot. HOWEVER, it may be better to just invest some of your time in that 4 1/2 minutes where he warms up to that point, to understand that he’s putting the positives AND the negatives in context, and looking at the bigger picture to recommend that we NOT mass-vaccinate.

He is saying that we should NOT mass-vaccinate IN SPITE OF the benefits that he lists and explains.

  • a decrease of disease in many countries
  • decline of morbidity and mortality rates
  • less illness in people who got vaccinated
  • severe disease is resisted even when vaccinees are infected with variants
  • they will shed much less virus than the unvaccinated, even when infected with variants
  • seropositivity rates are increasing in the population thanks to vaccination

But THAT is where he begins to disagree with mass vaccination. He states that we will NOT reach herd immunity, due to variants, and he explains this fully.


Global Problems of Sub-Optimal Mass Vaccination

At 28:00 minutes, Geert explains what we need to do – which is NOT what public officials are doing.

The current mass vaccination program will make things worse, in the long term. Geert explains then the kinds of vaccines we really need – vaccines which can both generate sterilizing immunity, AND which prime the immune systems of their recipients toward cellular immunity.

Yeah, it’s a bit of a tough goal, but it’s realistic toward the challenges of the China virus, and honest about what we need to do.

So what does this mean about the benefits of the vaccine?

THEY ARE REAL, BUT THEY ARE SHORT-SIGHTED. And they are accompanied by risks. Not just to the vaccinees, but to ALL OF US ON THIS PLANET.

According to Geert, continued vaccination is going to HARM vaccinees, relative to the unvaccinated, who will need to avoid virus-shedding vaccinees. At that point, recoverees may be in the best position of all, but still – not great. ALL of us will be in trouble from the virus which will escape the vaccines.

Geert also explains how we can prove that he is correct – by looking at the mutations in the virus which is shed from vaccinees, which will show selection for more infectious variants, if he is correct.

Now – this is a GREAT interview of Geert by Dana Loesch, who looks more and more like Sandra Bullock for some reason, but what the heck – the shotgun shells on her microphone setup are EXCELLENT, very non-Bullock, and she gets a FANTASTIC explanation of the problem from Geert.

Geert actually talks about Omicron, and the DANGER of it potentially evolving to be MORE SEVERE.

Take a listen!

Does Trump know this stuff? I don’t know.

I personally believe that Geert is right. I am now of the opinion that most of what we are hearing from Robert Malone, Peter McCullough, and Geert Vanden Bossche is true, but that each one has to give a little toward the ultimate truth.

What does that look like to me?

  • Natural immunity is NOT permanent or complete toward other variants
  • Natural immunity is better than the vaccines, generally speaking, but not bulletproof
  • Untreated COVID is a loser relative to the vaccines, but treated COVID is a winner
  • McCullough’s natural immunity prediction based on SARS1 may be too confident
  • Malone’s whistleblower on more shedding by vaccinees may have been wrong or disinformation
  • Geert’s vax-brag of less shedding by vaccinees may have been too kind and not skeptical enough
  • We have to stop pushing the vaccines, for the good of humanity
  • We have to allow the vaccines to continue, at an acceptably lower rate, for research
  • We have to allow vaccines to change faster, to keep up with mutations, IF and only IF this will not PUSH the virus to mutate and select faster (immune pressure must be low enough)
  • We have to pursue the superior vaccines that Geert is specifying
  • We have to use infection, treatment, and recovery as a big gun to reach herd immunity
  • We have to let COVID burn out of epidemic status, to reach a treatable endemic status
  • We cannot do that with mass vaccination, so mandates must cease promptly and completely
  • Joe Biden and CDC must be stopped – by military power if need be – if they will not end the crazy mandates

Yeah, you heard me. We can’t let this demented bozo, backed by an evil Obama and China, make COVID worse by mass vaccination. Mandates are making things worse.


Freedom, Vaccines and Morality

Trump may not understand Geert Vanden Bossche’s warning, but if we set that aside as an unknown, you can understand where Trump is coming from.

If we want freedom, we have to let other people make stupid choices that affect them most of all. Vaccination is, in fact, one of those things. Indeed, it is by US seeing it that way, that I believe we will end this nightmare of division which PUMPS UP the vaxxies and the crazy mandates.

In the same way that there are vaxxies who now are defending OUR freedom to be unvaccinated, I believe we have to defend the right of people to stupidly (or smartly) take the vaccine. However, we MUST get the rate of vaccination DOWN below the level where immune pressure from the vaccine creates more and more infectious variants.


The FIRST thing is not to take the vaccine yourself, or give it to your children.

The SECOND thing is to fight for an end to mandates.

The THIRD thing is to fight for BETTER vaccines, and to expand belief that the current vaccines are NOT GOOD ENOUGH, and are of the WRONG TYPE. Make the vaxxies demand better, not defend bad vaxxes.

The FOURTH thing is to spread the message that the “socially responsible thing to do” is to support Vanden Bossche’s position, that NOT taking the vaccine NOW is what will ultimately “save grandma”.

The last one is a hard sell, with FAKE NEWS pumping vaccine stupidity, but hey – we’ve fought tougher battles already.


So what about Trump?

Well, he is not in the position to know or respond to the “Geert Vanden Bossche Question”. Not yet. It is only when that issue becomes BURNING HOT, that Trump will be able to smartly push FORWARD from the current stupid CLOT SHOTS.

We will have to RAISE VACCINE CONSCIOUSNESS to levels of understanding that SUBVERT FAKE NEWS. We can only do that by getting most of the vaxxies on our side – to demand BETTER vaccines.

If they want to be guinea pigs – GREAT. They can be heroes, and try the deadly experimental vaccines. But we should NOT be forcing all of humanity to be part of a BAD and MISGUIDED experiment.

And the JOKERS who are allegedly running our military need to understand this. Virtue signals which kill troops, even if slowly and quietly, where nobody can see them, are NOT ACTUALLY VIRTUOUS. I appreciate them kicking out the sane ones who understand that the current bad clot shots may cripple readiness at some point, rather than forcibly injecting them. We WILL have a reserve of trained people who are not destroyed by China and Biden, no matter what China’s coming chess moves. Thank you for that. But as for everything else – there could have been push-back against communism, instead of acquiescence.

Yes, we had to be shown. But I’m not sure showing us subservience to a COUP and CHINA and FAKE NEWS isn’t undoing half of the good stuff.

But this as well. If you guys delivered Omicron on purpose, thanks. It LOOKS like it may be working.

Merry Christmas!

W

No New Bioweapon Under The Sun

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 PROBLEM, and that CDC was engaged in LYING, BLAME-SHIFTING, and HIDDEN AGENDAS.

And now the SCIENCE is coming out, and we were RIGHT.

We’re WINNING.

Another post discussed how – for whatever reasons are quietly embedded upon the length of the full spike protein and fragments thereof, chimeric or not – we are also now cursed with what appears to be, to some [currently socially tolerable] extent, an abortion virus and abortion vaccines.

Trust me – THAT is a trumpet that BRINGS DOWN WALLS.

We may even have a scientifically sound explanation for the craziest reports of vaccine side effects in the close but unvaccinated – namely, hormonal activities that are operating at the low microgram level.

Oxytocin – abortion dose = 10-30 IU = 16-50 mcg


Let me explain how that works. Think “DUST”.

I can tell you all about the potency of carfentanil. ONE BREATH of inhaled dust containing a tiny amount of it knocked me out like a roundhouse to the left jaw. If that ENTIRE DUST had been carfentanil, I would have been DEAD. But there was a fraction – a tiny fraction – of that tiny grain you see right there, that got into my lungs, riding on OTHER DUST, and I was OUT LIKE A LIGHT.

NOW you understand the POWER of the spike protein.

Yes, there is SO MUCH that they HIDE FROM US to maintain POWER OVER US.

However, now I want to put ALL of this virology technology into DEEP PERSPECTIVE.

“Black goo” biological agent in the movie Prometheus, part of the “Alien” franchise.

What I am going to tell you is almost certain to shock you – both about the disease and about the vaccine. It shocked me. That’s why I figured I had to explain this to people.

And what’s even WEIRDER – this is not totally about the disease or the vaccines, but also about their CONTEXT, which forces you to SEE them both differently and more CLEARLY.

A while back, I was just browsing the “edutainment” about viruses on the internet, when I was led down an interesting rabbit hole of viruses in entomology. You know – INSECTS. I read something on Wikipedia which bothered me, so I set it aside. It all seemed FAR too familiar. It surely impacted all this crap we’re going through now – I just wasn’t sure how. Later I came back and read it again.

Now, I understand. It’s actually rather beautiful. But – well – it’s interesting.

The greatest point being – THERE IS NOTHING NEW UNDER THE SUN.

The great irony of the idea “nothing new under the sun” is the self-referential part – the idea that EVEN this little bit of wisdom is with certainty not even attributable to its first alleged “author”, who HIMSELF surely understood the great irony of his saying it, and that others might attribute it to him, someday.

Nothing new under the sun. This bit of Solomonian passed-on wisdom about the curation rather than creation of wisdom is far truer than I realized. Let’s EXPAND just a bit.

The idea that this universe is as old as it appears to be, and that in all that time, Einstein was the first person (using the term rather broadly) to discover the logic of how speed actually works, strikes me as a violation of Solomon’s logic about “first discovery” being rare as hen’s teeth.

Likewise, Solomon’s logic goes further and tells me that “hen’s teeth” undoubtedly happened a lot more often than, when in its earthly rarity, it happened “here and almost now”, but seemingly only roughly once.

Rarity being somewhat relative, with distance providing a deceptive but effective cover for number and frequency, all of them together being a control of wisdom over knowledge.

Yet even these seeming corollaries of the idea of “nothing new under the sun” are just repeats of the idea with some frill on the edges enlightened for our benefit.

“…it is curiosity that gives meaning and savour to life.”

LIFE. Seems to be part of the design. No?

Have I BOTHERED you yet?

Maybe even a bit of trepidation – or even FEAR?

Good. THAT has happened before. “Nothing new under the sun.”

You can never go wrong with Solomon.



The Last Time Gene Therapy Was Reinvented

I keep trying to tell people – DNA is very smart. We are slowly learning how to talk to it. Sometimes we actually listen. Sometimes we even plagiarize.

DNA bargains and wheedles its way into the future, changing in whatever ways it has to, to keep itself alive. It gains as much vision of the future and the past that it can, using proteins, to persist as well as it can.

Think of it this way. DNA fights and feuds with DNA, but who wins in the end?

DNA.

NOTHING that these foolish young humans are trying to do with their coronaviruses, their “vaccines”, and their “gene therapy” is new to DNA. DNA came up with ALL of this stuff – AGAIN – at least 100 million years ago. THAT was its destiny. Ironically repeating like its own form.

I am absolutely serious. The technology of EVERY one of our wonderful new coronavirus vaccines (or “injections” or “gene therapies”, if you prefer) was RE-invented by DNA approximately 70-100 million years ago on this planet, and is still around.

ONE example of a prior reinvention of gene therapy resides in a tiny biological war-game where THREE organisms cut a deal that keeps them all alive. I will point out all of the “original versions” to you, and you will see where human science basically plagiarized.

One of the three organisms is an insect – a kind of wasp – that gravitated into using a living host for reliable reproduction. The second is a voracious plant-predatory host insect – a caterpillar – that needs a dependent predator to keep its numbers in steady balance, because it won’t do it itself. The third is a virus that found a way to survive by helping insure that the host-guest “life transfer” process always succeeded, so that it, too, would survive.

DNA uses ALL OF THEM to optimally persist.

The key to understanding all of this, is a kind of virus called a “polydnavirus”. I personally like to pronounce that “Poe-LID-na-virus”, even though that is wrong. They’re actually supposed to be called “Polly-D-N-A-virus”. My advice is pick whatever you like – you’re probably never going to have to say the word publicly – and on the internet, your canine pronunciation is always perfect.

Or just call them PDVs.

Wikipedia’s entry for them is an excellent place to start.

LINK: https://en.wikipedia.org/wiki/Polydnavirus

ARCHIVE: https://archive.fo/YHP7V

The bottom line is very simple. The wasp lays its eggs INSIDE a caterpillar by injection. However, instead of injecting a mere venom along with the egg – a kind of chemical weapon – the wasp injects a venom containing a VIRUS – a biological weapon. The virus provides biological effects like immune suppression that HELP the wasp egg survive, hatch, and grow. This is much more efficient than merely injecting, say, immunosuppressive proteins in the venom. The immune suppression by the virus prevents immune response by caterpillar cells known as hemocytes.

All of that is shown in the following graphic.

Here is one of the first really fascinating aspects of these polydnaviruses. When they are in the wasp, they are actually PART of the wasp genome. That’s right. They’re IN THE WASP’S CHROMOSOMES. The virus is now PART of the wasp’s genetics. One could even view it as the wasp sending PART OF ITS OWN GENES into the host, to make sure that the egg survives.

When the virus is still inside the wasp, it only comes out of the genes and reproduces in one place, in FEMALE wasps, near where the eggs are formed. It doesn’t harm the wasp, because DNA is NOT stupid. Viral DNA learned – the hard way – don’t shoot the pilot. Just stay in your seat until it’s time to debark. Wasp DNA learned – the hard way – let the jihadists sleep until we get to the airport we want them to shoot up. All of it mediated through the most annoying code in the world, with zero comments and nearly inscrutable, almost accidental language.

You remember those “well, it works” phone calls, coders. “I don’t know. Try this.”

Now – the next point is even cooler – because it’s the exact same strategy as the coronavirus vaccines that use viral vectors (e.g., Johnson+Johnson, Oxford/AstraZeneca, Sputnik V).

The infection does not lead to replication of new viruses, rather it affects the caterpillar’s immune system, as the virion carries virulence genes instead of viral replication genes.[4] They can be considered a type of viral vectors.[5]

Wikipedia, https://en.wikipedia.org/wiki/Polydnavirus#Biology

The virus particles that are sent into the caterpillar are NOT reproductive – they are merely infective. They don’t code for creation of new virus, which might reproduce exponentially and kill the host or use up too many resources. Instead, the infective non-reproductive virus particles – just like the coronavirus vaccines – give a nice, predictable amount of expression of new proteins, useful for the wasp eggs and larvae to prosper. The virus basically CONSERVES caterpillar so that it has a ticket and a ride OUT of the dead caterpillar when it’s all over.

That’s the EXACT same strategy as our mRNA and DNA vaccines. Don’t crank out too much spike protein, by cranking out any new virus, and thereby kill the host. The main point is SAVING the host. The point may also be STERILIZING the host, to some extent, because THAT protein effect is beneficial to the injecting parasites known as the Democrat Party, globalist banks, and China. And probably more than one type of pencilneck. But they do want us to live – at least for some time, it would appear.

But seriously – the wasp polydnavirus immunosuppression strategy IS the human adenovirus vaccination strategy.

The only difference is what the proteins that are created DO. In the caterpillar, they suppress the immune system response to the egg or larva. In humans, the one protein stimulates antibodies to itself, and possibly does other things which are intended or not.

So you may be wondering how the virus gets from parent wasp to child wasp if the virus that is sent into the caterpillar host is not reproductive. AHA. It is because the virus is tucked into the GENOME of the baby wasp, safe and sound, for a ride into the future. The virus genome is essentially protected by the wasp.

LINK: https://www.microbiologyresearch.org/content/journal/jgv/10.1099/0022-1317-77-11-2873

Thus, you can see how genetic incorporation of the VIRUS benefits BOTH the wasp and the virus – and even – in a weird way – the caterpillar. The wasp gets to control the genetics and expression of the virus, so that they don’t cause the wasp too much trouble, but instead yield maximum benefit. The virus can then be more effective at its now exclusively delegated task of immune suppression in the caterpillar, by relinquishing reproduction to the wasp. Division of labor creates a great mutual dependency, but it also creates a strong contract.

One could say that genetic incorporation is a STRONGER CONTRACT between the virus and the wasp.

Just like genetic incorporation of COVID-19 spike protein could be a STRONGER CONTRACT of reduced human fertility.

But how does the caterpillar benefit?

The caterpillar is not going to live on as THAT particular caterpillar, but THAT particular baby caterpillar-culling wasp will live on in an assured 1:1 trade-off, and the REST of the caterpillars which benefit by the current culling will also live on as a stable population. The C-W-V balance is maintained BETTER by seeking a more stable chaotic resonance, without the wild swings of boom and bust, if wasp reproduction and population can be more closely tied to the caterpillar population, and they all live into the future without wild swings in numbers.

Another way to view it from the caterpillar perspective, is that viral efficiency minimizes the number of sacrificial caterpillars needed to keep the necessary number of wasps alive.

Now – we’ve seen viral vector vaccines analogous to the non-reproductive but infective polydnavirus virus particles – those would be the Johnson-+Johnson, AstraZeneca, and Sputnik V vaccines, which use adenoviral vectors for non-reproducing, protein-creating, virus DNA. But what about the Pfizer and Moderna vaccines?

Well, it turns out that these {{{wasps + viruses}}} invented ANOTHER way to get DNA or RNA into the caterpillar host – those are called VLP, for “virus-like particles”. There is a lot of range and variability here, just as there is in non-viral-vector vaccine technology. So in the same way that the Pfizer, Moderna and Inovio vaccines use proprietary “virus-like lipid droplet nanotechnology” to get their mRNA or DNA into human cells and thus cranking out spike protein, wasp/virus DNA can also use a strategy of “virus-like particles” that don’t even mimic non-working viruses, and STILL get their effective DNA transferred to the caterpillar, to effect the desired expression of needed wasp/virus proteins in the caterpillar.

Now – that is not to say that PDV (polydnaviruses) and VLP (virus-like particles) are the only tricks up the ovipositors of these parasitic wasps. It turns out that – in addition to these well-described DNA viruses, there are also apparently RNA viruses which ride along with wasp eggs during injection. So YES – both DNA and RNA “vaccines” are part of the wasp injections. And YES – there can be genetic incorporation in the caterpillar cells – for their short lifespan – just as there is already genetic incorporation, long-term, in the wasps.

Remember – who wins? DNA WINS. The HOUSE always wins.

But don’t forget Novavax! It may just be protein, but protein shills for DNA!

Not only are the Novavax “pseudo-viral protein-based nanoparticles” already examples of virus-like particles – they are matched by protein-based components of the wasp venom, both free-floating or otherwise. Indeed, one cannot read about the virus-like spiked particles in this wasp venom and not think that Novavax design is pretty much the same thing.

NOW – this is all a LOT to unpack. Not just that, but my “dumbing it down” probably made it just plain dumber. To correct that, I’m going to let the experts FIX THINGS UP.

The field of polydnaviruses in insects is NOT a huge field. It’s actually rather obscure, despite the phenomenal importance we are witnessing now. Just as the media can help those in power hype and control a field like climate science, or literally HIDE certain other fields like [[[ COUGH ]]], they can obscure still other fields which radically affect you, by hiding them pretty much in plain sight.

There is a BOOK that reviews the field, however, which is EXTREMELY helpful.

You can download parts of this book, and that includes TWO parts which are more than enough for a reasonably smart normal person to see the CONTEXT EXPLAINED.

Let me get ONE of those parts out of the way because you’re not going to be interested in this, unless you’re ready to get VERY nerdy on the history of science. But I am including it because it is AMAZING STUFF. You might view this as “The history of the science of the rediscovery of all the evolutionarily discovered technology used in the “vaccines” or “shots” or “gene therapy” of the coronavirus genetic injections”. It’s a beautiful window into HOW SCIENCE WORKS.

Foreword – The Discovery of Polydnaviruses and the Influence of Dr. George Salt

You can download a PDF of this at the linked page.

Now – if you read that – you will get a LOT, including a window into the slow and painful nature of research, but it’s a bit difficult to extract the good stuff if you’re not used to reading scientific review literature.

In contrast, the PREFACE of the book is MUCH easier to read, and it puts ALL this stuff in context that normal humans who are not experts in polydnaviruses can understand.

Preface – Parasitoid Viruses – Symbionts and Pathogens

I highly encourage you to read the full preface at the linked page. But what I’m going to do here is simply pull out all kinds of juicy quotes – which is damn near the whole thing. [ My comments ] and identified WOW sequences will be in bold.

Here we go – this is all quoting:


Among parasitoid viruses, the fascinating models of polydnaviruses (PDVs) were discovered in the 1970s and the new field of polydnavirology was thus opened.

This field has been moving very fast since the beginning of the century thanks to the use of genomic approaches and rapid expansion of accessible databases on insect and viral gene sequences.

Parasitoid and viral genomic studies have confirmed that PDVs are functionally gene transfer agents used by parasitoid wasps to manipulate the physiology of their parasitized lepidopteran hosts by introducing modified versions of their own genes into host cells.

In the case of PDVs from braconid wasps, this kind of gene therapy (detrimental for the patient, which is in this case the lepidopteran host!) originated from the integration of a virus genome in a wasp genome ca. 100 million years ago. [LOL – I just noticed this “being impressed by the date” part – looks like we BOTH realized this independently. -Wolf]

This virus has been modified to incorporate wasp genes instead of its own viral genome in the nucleocapsids inside the viral particles. [Minor beef here – ownership and original genetic penmanship on the payload could be more “virus” and less “wasp” – interesting problem.]

Such use of viruses as vectors has been selected several times independently during the evolution of parasitoid wasps. [There it is. VIRAL VECTORS. Invented by DNA.]

The PDVs associated with braconid and ichneumonid wasps (Campopleginae subfamily) are unrelated as judged from the machinery producing the particles, and they represent an example of convergent evolution with different viral origins.

A third association event is suspected to have occurred in the Banchinae subfamily of ichneumonid wasps. In essence, the parasitoids have ‘captured’ viral elements that have evolved a host regulatory role that benefits the parasitoid to facilitate successful parasitism. [This is more “archaeopteryx” on the payload being of viral origin.]

Other associations with viruses or virus-like particles might have evolved with different organisms but they have not been unraveled yet, and parasitic amoebae that have associations with mammalian viruses are just one example. [“Lots of room at the bottom.”]

Many insects have evolved associations with a large number of species of bacteria such as Wolbachia and associations with viruses have been less well studied to date compared to bacterial symbionts.

A number of different viruses are found in the genital tract of the parasitoid wasps and conceivably they could be transferred to female wasps by behavioral traits, such as host feeding, initiated following ovipositor puncture of the surface of the integument.

Host feeding may thus be an advantageous behavior for viruses which facilitates their spread within insect populations and this intimate association with viruses might have favored interactions leading in some cases to integration of viral sequences into the wasp genome, although most of the wasps described in this book are no longer host feeders.

These viruses include RNA viruses of insect parasitoids and most of them appear nonpathogenic. Could these likewise have evolved a symbiotic relationship with their host? Future research may reveal such an intimate relationship with the wasp host carrying them but, currently, we have little information about their functional role as symbionts or pathogens in the virus–wasp–insect host relationship. [This was in 2012 – the situation could be different now.]

While the study of polydnaviruses was initially inspired by the pioneering studies of George Salt and Susan Rotheram at Cambridge University, more recent studies of Venturia (formerly Nemeritis) canescens particles (the virus-like agent studied by George Salt) by Otto Schmidt and Sassan Asgari documented that these virus-like virions lack both DNA and RNA; the particles are comprised of proteins encoded by parasitoid genes. [This is basically virus-like particle nanotechnology akin to the Novavax vaccine.]

The multiplicity of different molecular forms seen in these viruses and virus-like particles is truly amazing but, compared to polydnaviruses, we have less information about the biology of virus-like particles and how they function. [There is clearly an infinitude of possibility here – clearly WHY the push for gene therapy.]

Finally, not all parasitoid species are associated with viruses and most in this category have to rely on virulence factors produced by their ovaries and venom glands instead of using the host to produce them like for PDV-encoded gene products. [Translation – most of the wasps use plain old venom.]

PDV-associated species also produce venom that was shown in some cases to synergize the effect of the virus. [Combination biological and chemical weaponry.]

New sequencing approaches are more comprehensive and will thus allow comparisons of the arsenal of proteins used in different species, which will enhance our understanding of the dynamics of evolution of parasitoid virulence strategies. [Big data will allow spying on the past to happen even faster.]

Ectoparasitic wasps have not been examined yet for the presence of viral symbionts, and appear to have exploited venoms as a source of host regulatory molecules instead. Comparative studies on paralyzing versus nonparalytic venoms are lacking, and screening ectoparasitic species for viral elements should also be a future research priority. [Translation: there’s more to learn from regular stinging / paralyzing wasps.]

In addition to enhancing our knowledge of parasitoid strategies and increasing our understanding of the importance of symbiotic relationships in species evolution, parasitoid viruses and venoms may constitute a source of new molecules to control insect pests. This might be a revolutionary outcome of research on PDVs and other parasitoid viruses, since the safety of many chemical pesticides with respect to their detrimental impacts on human health and key species in the environment such as bees and other beneficial insects, is questioned. [You think proteins are going to be safer? HA! Get ready for new problems.] We anticipate that harvesting biopesticidal molecules from parasitoid venoms will likewise prove fruitful. [Translation: All this human wasp techno coronavirus lying crap is headed to agriculture, and presumably already there. Yeah.]

Finally, we hope that this book will satisfy the reader by presenting an overview of the most recent findings on all these topics presented by an international assemblage of authors. [You can say that again!]

In addition, we aim to inspire many future researchers to choose polydnavirology or studies of other parasitoid viruses or viral-like elements and venoms as their focus field. [You’ve inspired me, even though it’s a bit late for me to enroll in one more Marxist university.]


That’s it.

I tell you – this whole thing was a revelation. Suddenly, everything these people in Big Pharma have been doing has been HUMBLED BY GOD, using BUGS. LOL! Pretty amazing.

And being humbled, all of us, the TRUTH now becomes clear.

Now – if all this seems a bit scary, but you’re thinking “Hey, this isn’t exactly like our case, in which Democrats mind-fracked their victims with an RNA virus” – well, HOLD YOUR BEERS. With God – IRONICALLY – all things are possible.

Yes, this, too – baffling the victim with an RNA virus – was borrowed from nature, although I am being just a wee bit facetious, since it was done much more intelligently and much more socially against a more intelligent and social species.


The Case of the Shanghaied Babysitter

Yeah, I’ll try to keep this one shorter, but I don’t really have to go back TOO MUCH to the original literature here.

Here is where I FOUND this case originally. An article that was COPIED onto a forum.

Parasitic wasp uses virus to control its host

LINK: https://forums.spacebattles.com/threads/parasitic-wasp-uses-virus-to-control-its-host.332664/

The links back to this forum article are ALL bad, but I was able to google for correct ones. Here is the article in Discover Magazine:

Biological Warfare: Parasitic Wasp Uses A Virus To Control Its Host

Science Sushi By Christie Wilcox Feb 11, 2015 2:36 AM

LINK: https://www.discovermagazine.com/planet-earth/biological-warfare-parasitic-wasp-uses-a-virus-to-control-its-host

THAT article goes back to THIS scientific literature:

LINK: https://royalsocietypublishing.org/doi/10.1098/rspb.2014.2773

This is actually a very long and complete scientific article. Let me give you the “TL;DR” version.

When the wasp lays an egg in the ladybug, it also injects an RNA virus. That virus makes the ladybug go “mask Karen” crazy, and stick around and GUARD the pupated larval wasp after it emerges from the ladybug and cocoons. The ladybug may then even kick the virus and go on living after the young wasp departs.

Yeah, let me HIGH FIVE that long-hauler ladybug.

Just sayin’.

Democrats.

SPIT.

SO – where are we now?


Is Phony Gene Therapy About Population Control?

We have now looked at the COVER PRESENT (coronavirus and vaccines), the EFFECTIVE PRESENT (spike protein virus and vaccines), the LIKELY DEEPER MOTIVATING PRESENT (contraceptive / abortive virus and “vaccines” that look pretty much like public “health” gene therapy), and the PURPOSED ORIGINAL HONEST PAST (infection and/or genetic modification of the injected to produce desired effects using RNA viruses and/or specialized viral vectors) – the latter insect past being a lot like what is happening now.

Are you ready for the FUTURE?

Well, there’s a lot of range on that. Maybe it’s THIS…..


Now I know a lot of y’all are, like me, saying “Yeah, that will be a cold day in hell!” But let’s consider it anyway. It helps to understand things.

WHY would Hillary say this, about Trump’s possible winning in 2016?

What crime could POSSIBLY send hundreds of historic conspirators to some horrible fate like what happened to the NAZIS? They would have had to have done something even more horrible – right?

Well, viewed in “holocaust” (small “h”) terms, an “abortion virus” followed by “abortion vaccines” might count.

It’s a pretty ingenious idea. If you honestly believe that overpopulation threatens the planet, and that stopping it “by any means necessary” is justified, then the idea of:

  • taking a modifiable cold virus but…..
  • don’t call it that, so people will be AFRAID
  • warm up the FEAR CROWD with SARS, Ebola, Zika, etc.
  • use a cold with its own moderate antiprogestogenic or oxytocin hormonal activity, or some other way of exerting a contraceptive or abortive activity
  • optionally increase that activity
  • release the virus
  • create vaccines with the same effect
  • require ongoing vaccines to titrate the effect on society

To me, this is very much like the wasp strategy, only instead of hijacking the juvenile butterfly with immunosuppressive negative gene therapy in a PRO-FERTILITY strategy for its own offspring, what the Democrats are doing is an ANTI-FERTILITY strategy using progestosuppressive negative gene therapy on basically all humans who are not in on the scam. And they also used an RNA virus to mess with our minds, though THAT was a bit artful, shall we say.

Now, I think the success or failure of their operation is going to depend on the ultimate level of contraception that is achieved here. The effect on society will depend on whether the Dems, globalists, and Chinese are trying to pull off a very steep and fast population drop that would generate a social immune reaction, or a long, slow, incremental one that would not. We probably won’t know this for several years.

But just consider this “back of the envelope” calculation.

Let’s say that Demmunists require 2 coronavirus boosters every year. Say that between compliance and effectiveness, ONE of those boosters is effectively pregnancy-blocking for any pregnancy currently in process. Run this over all of humanity, so that once every year, every woman is hit with a “menstruation and miscarriage vaccine” using the spike protein. With a pregnancy window of 75% of the year, that target is the broad side of a barn, as long as CDC continues to insist that it’s safe for pregnant women, or women who are trying to become pregnant. You would get massive observable menstruation and miscarriages after vaccination, and the plot would not last.

It’s not a SUSTAINABLE LIE.

BUT – as long as the effect is random, subtle, and single-digits, it can be hidden by a compliant scientific community, which is socially conditioned to reject the truth. Even bigger, control of social media, communications, and other avenues of discovering the truth, mean society can be kept completely blind to a subtle population control.

But seriously – reducing the fertility of humans by 5% is a BIG DEAL. It doesn’t mean it’s the end of it. It’s a GOOD BEGINNING – from their point of view.

You’ve got to look at this thing, like you’re trying to pull it off, to see that you really COULD pull it off.

And if we could pull it off, they will pull it off.

So – that’s where I’m at.

And if I’m right, they will NEVER FACE JUSTICE for what they’re doing.

So here is a rule about Democrats.

Democrats, China and other communists will always pick an unjust fait accompli over a just agreement.

Thus, as long as they do things where the price of tolerating their crimes is less than the cost of a civil war, they will just keep doing those things.

Something to think about.

W

Are Clotting Problems a General Minor Risk of COVID Vaccines?

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. He has a REALLY GOOD explanation of relative risks, so you can understand why the decision was made to limit, at least temporarily, distribution of the AstraZeneca vaccine, in various countries.

One important thing that Dr. ZDogg notes, is that – because the Johnson+Johnson vaccine is similar to the AstraZeneca vaccine, both being DNA vaccines and both being adenovirus vector vaccines, it is possible that the J+J vaccine might also have the same rare side effect as the AstraZeneca vaccine. This possibility is now being scrutinized carefully.

I mentioned the above video in my previous post on the Johnson+Johnson vaccine:


Johnson+Johnson Vaccine Follows Pfizer, Moderna, and AstraZeneca into Problem Territory, and Proves Once Again – Clinical Trials Have Limits

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 …


In that post, I noted that one critical difference between the AstraZeneca vaccine, which uses DNA and viral vectors, and the Johnson+Johnson vaccine which uses the same, is that the AstraZeneca vaccine also does NOT use the “2P mutation” in the spike protein, which almost everybody else among the early players (Pfizer, Moderna, J+J, Novavax) does use it.

That would seem to potentially suggest that the problem of vaccine-induced thrombotic disorders could be limited to the AstraZeneca vaccine.

Well, first of all, it looks like the J+J vaccine also has the clotting problems.

Six women developed blood clots after the J+J vaccine, and one of them died.

Yes, it’s relatively rare, but it looks causitive.

And also, this article:

…..suggests that there MAY be something LIKE the AstraZeneca problem, known as vaccine-induced prothrombotic immune thrombocytopenia (VIPIT), going on with BOTH Pfizer and Moderna.

This case was actually covered by the Daily Mail in blaring headlines on January 6 and 7, 2021. Kind of obvious NOW why this got memory-holed!


EXCLUSIVE: Wife of ‘perfectly healthy’ Miami doctor, 56, who died of a blood disorder 16 days after getting Pfizer Covid-19 vaccine is certain it was triggered by the jab, as drug giant investigates first death with a suspected link to shot

  • Beloved Miami obstetrician Gregory Michael, 56, died following a suspected catastrophic reaction to the Pfizer Covid-19 vaccine, DailyMail.com can reveal
  • Heidi Neckelmann says her husband was completely healthy until he had the jab on December 18 at Mount Sinai Medical Center 
  • He succumbed this week to a stroke brought on by acute IDP – Idiopathic thrombocytopenic purpura – a blood disorder caused by a lack of platelets
  • IDP can be acute or chronic, lasting six months or more, striking on its own or in conjunction with other autoimmune conditions or certain cancers 
  • Heidi insists, however, that her husband did not have an immune disorder or any similar condition that could have caused ITP 
  • The mother-of-one said: ‘In my mind his death was 100 percent linked to the vaccine. There is no other explanation’  
  • She said: ‘My husband had conversations with the doctors who said it was highly probable that the vaccine was the cause’
  •  If his death is linked directly to the vaccine, Michael would be the first known case in the world of a person dying after the injection
  • A spokesman for Pfizer told DailyMail.com the firm was looking into Gregory’s death but they did not believe it had any link to the vaccine 

By BEN ASHFORD FOR DAILYMAIL.COM

PUBLISHED: 18:54 EDT, 6 January 2021 | UPDATED: 12:16 EDT, 7 January 2021


Despite the bad timing earlier, it’s getting a lot more attention now.

There may also be other problems with the Pfizer vaccine that are being lost simply due to the ages of the patients.

CNA Nursing Home Whistleblower: Seniors Are DYING LIKE FLIES After COVID Injections! SPEAK OUT!!!

HealthImpactNews Published January 26, 2021 303,563 Views
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It’s definitely time to look at the data in hand, very carefully.

This is going to help us all look at relative risks properly now, IMO.

John Fink and James Coburn discuss case in a scene from the film ‘The Carey Treatment’, 1972. (Photo by Metro-Goldwyn-Mayer/Getty Images)

It’s going to help us understand what’s really going on.

Title: CAREY TREATMENT, THE ¥ Pers: COBURN, JAMES / AUBREY, SKYE ¥ Year: 1972 ¥ Dir: EDWARDS, BLAKE ¥ Ref: CAR019AF ¥ Credit: [ MGM / THE KOBAL COLLECTION ]

And that’s a good thing.

W

John Fink, James Coburn, and Jennifer O’Neill having a meal in a scene from the film ‘The Carey Treatment’, 1972. (Photo by Metro-Goldwyn-Mayer/Getty Images)

Johnson+Johnson Vaccine Follows Pfizer, Moderna, and AstraZeneca into Problem Territory, and Proves Once Again – Clinical Trials Have Limits

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 explanation of the AstraZeneca problem and what people are doing about it.

You will note that Dr. ZDogg, MD points the J+J vaccine being at risk of having the same clotting problem as the AstraZeneca vaccine, due to them BOTH using DNA (as opposed to mRNA) and viral vector (as opposed to liposome) delivery technologies.

I just learned something today from C&EN that may impact this.

https://cen.acs.org/pharmaceuticals/vaccines/UT-Austin-Mount-Sinai-partner/99/i13

It turns out that Pfizer, Moderna and J+J are ALL using the “2P mutation” of the spike protein, but AstraZeneca is not. This mutation significantly CHANGES the spike protein, preventing it from leaving the “pre-attack” molecular shape.

Is THAT the difference? Does the 2P mutation prevent the spike protein from causing problems? Stay tuned! The J+J vaccine will get intense scrutiny going forward.

Now – J+J has had a problem of being WEAK from the very beginning, but STATISTICALLY it has still shifted people AWAY from being hospitalized or dying. People may have still caught the disease after vaccination, but they were never going to the hospital or dying – a LOT like hydroxychloroquine administered early, or better still, the Zelenko protocol.

A short while back, one gal in New York got COVID about a month after getting J&J.

Brooklyn woman gets COVID 3 weeks after Johnson & Johnson vaccine

She was not hospitalized. This was a living example of the admitted weakness of the J+J vaccine. NOW, however, somebody who got J+J DID get COVID and DID go to the hospital, so the “promise” you will not go to the hospital with the J+J vaccine just got a bit weaker.

Man in hospital with COVID-19 after receiving Johnson & Johnson vaccine

Will J+J go to a 2-shot booster program? Hmmmmmm.

My bottom line?

I like waiting for the results to come in from the PHASE IV “Hold My Beer” TRIALS. Particularly since I’ve already HAD the disease.

W

Wolf’s Red-Hot Date With Retrotranscriptive Faucipox

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 OF THE SCAM gets ahead of them. CDC is lying to us so badly. SO badly.

It’s all good, people. I’m on these bastards like BLACK on TAR.

Notice that the governor’s WIFE also tested positive later. But most importantly, notice how the news never asks the RIGHT QUESTIONS connecting the vaccine to the positive test. Instead, we get LIES.

Example: https://www.cnn.com/2021/04/06/politics/greg-gianforte-montana-governor-tests-positive-covid/index.html

Archive: https://archive.fo/PV9pN

The FAKE NEWS is going along with this crap. They are so deep in this.

Yes, we are now in peak MITHRIDATISM that they wanted to turn into the MIDAS TOUCH of SPIKE PROTEIN.

Such a SCAM.

In my opinion, the CDC should be CLOSED as a CRIME SCENE.

Thank you, Greg. You are a SCIENTIST, and when you felt SYMPTOMS you forced them into coughing up the DATA that reveals how badly they SCAMMED us, and how badly they continue to scam us.

I think Fauci knows exactly what I know. He could tell you EXACTLY why this happened. And once Rand Paul reads this, he’ll know, too. Somebody needs to start cornering Fauci on all this crap.

It ALL goes somewhere.

LOOSE SCIENCE that you know and everybody else doesn’t is a MAGIC ACT. BAD FAUCI!

I’m seeing into the psy-op, people. I’m seeing so deeply.

THE SPIKE MUST FLOW. AND FLOW AND FLOW AND FLOW. It’s the KEY to the SCAM.

Once you see the spike protein CORRECTLY, you see why they do everything they do.

How much you want to bet Bill Gates is wise to this stuff?


Real Preface

I have come to the conclusion that something is very wrong with COVID-19 and the vaccines thereof, and I think I’ve finally put my finger on the scientific macguffin that ties all the skeevy, sketchy stuff together – reverse transcription.

That would be that little red arrow back to DNA from RNA.

It turns out that reverse transcription, and vaccines for diseases that might code for it, are very “Fauci”.

Learn to code. It’s KEY.

Too many things “political, organizational, governmental, and media” have not added up about the phony “plague”. Going beyond that, too much SCIENCE about the “novel coronavirus” and vaccines being offered for them, simply did not add up.

At least, not until now.

It’s not my inner conspiracy theorist which is finding a problem here – it’s my inner scientist. I am having great difficulties rationalizing certain seemingly careless choices which have resulted in some of the most problematic and badly framed medical offerings since “eye of newt” and “really large leeches for anemia“.

I am having a scientific problem with TESTING that is so bad – so intentionally bad – that it borders on the freaking Ouija Board.

And FAUCI KNEW.

It’s all the result of DISHONEST SCIENCE.


Background: “Science Is Real”

I’m not exactly anti-science, having worked in science all my life. I’m not even opposed to “transhumanism”, which I don’t think is inherently and necessarily BAD. The idea of expanding my memory without putting Google or Facebook or anybody else in charge of it? Talk to me. I’m listening.

I’ve ALWAYS gotten the flu vaccine – ALWAYS. I NEVER miss it. That’s not exactly transhumanism, but it shows that, for most of my life, I had great TRUST in medical science. In fact, I would even say I still do. Generally speaking.

I’ve had vaccines for everything I could get – even the RABIES vaccine, when I was bitten by a bat. The rabies vaccine is, in fact, one of the STRONGEST defenses of vaccination in medical history. No vaccine opponent WILL or SHOULD turn down the rabies vaccine – it is a HUGE success story in medicine. If you get bitten by a rabid animal, the rabies vaccine promptly administered against that SLOW virus will SAVE YOUR LIFE. Some vaccines are of arguable worth, but the rabies vaccine is not one of them.

Indeed, I consider myself to be something of a gourmet, or at the very least a connoisseur of vaccines. Previous “reviews” of vaccines on this site have featured my lovely assistant, Miss Direction, née Retroculture, who helps me convince people that vaccines weren’t always questionable, and might even be good for people.


Wolf’s Hot Date With Retrosynthetic Dinopox

Hey, it’s not every day that I get to post something that’s not only about the unspeakable issue of vaccines, but is both PRO-VAX and ANTI-VAX at the same time. I mean, what’s the use of FREE SPEECH if we can’t use it to troll EVERYBODY – including PENCILNECK? Whoops – WRONG PENCILNECK. Let’s try …


Wolf’s Chill Second Date With Retrosynthetic Dinopox

Perhaps you recall my PREVIOUS correspondence and “review” of the new, two-shot shingles vaccine, Shingrix – or more specifically, my review of the FIRST SHOT. Wolf’s Hot Date With Retrosynthetic Dinopox Hey, it’s not every day that I get to post something that’s not only about the unspeakable issue of vaccines, but is both PRO-VAX and …


I was anticipating getting one of the new coronavirus vaccines – and was holding out for the first one PROVEN to be safe for recoverees from COVID-19, one of whom I happen to be.

My lungs aren’t that good anymore – not after COVID-19 seared them like some kind of biological chlorine gassing on the front lines in France. I have to be very careful. Another case of COVID, or pulmonary / vascular coronavirus vaccine side effects of comparable severity, might actually “finish me off”.

So – I’m SHOPPING. And I mean SMART SHOPPING. I’ve been paying a LOT of attention to the new vaccines, and trying to understand their technologies, their benefits, their risks, and the science behind them. I simply can’t afford to make a mistake on side effects. Not if I want to enjoy the retirement for which I worked LONG and HARD.

I already knew quite a bit of the science behind COVID and the new vaccines – enough that it has been easy for me to follow the scientific news about these things. I’m not a virologist, an epidemiologist, a vaccine expert, or a molecular biologist, but I’ve worked with such people for much of my life. I picked up a few key ideas in the process. I’ve also come up with a few scientific ideas and principles of my own, but that is largely because I’m a devotee of the history of science, which gives perspective on science.

If you don’t think science can be WRONG, and that large numbers – HERDS – of scientists therein, can go OVER A CLIFF, just take a look at Planet Vulcan, Lysenkoism, The Great Leap Forward, and science in the Third Reich – a seminar on the latter having been quite instructive in my youth. It was not simple how the scientific masses in Germany were led astray, once socialist politics DRAGGED, PUSHED, and SCARED them away from “Jewish Science”. The top echelons of German science, filled with Jews and their friends and spouses, were forced into horrible choices, as some of the best science and scientists were politically rejected over a real social stupidity which fractured and destroyed what was arguably the leading scientific nation on the planet.

None of that had to happen – but it did.

Don’t think we’re immune from scientific debacle. We’re not. Socialism is the greatest “hold my beer” knucklehead that science ever green-lighted into a dysfunctional relationship. He’s always coming back on Saturday night with roses and cherry vodka, after the “last” last time he wrecked Science’s cute little sports car.

Science normally checks itself for errors – and it is my contention that the checking needs to be extensive – all the way out to society as a whole – including stakeholder scientists, non-stakeholder scientists, and even the non-scientific public at large. Sure, you can skip the non-stakeholders and the public, but is it wise? Hardly, in my opinion. The smaller the group needing to be fooled, the easier it is to accomplish things which society simply does not want, or which have vast intended or unintended consequences.

Yuri Geller proved that scientists are easy to fool. James Randi made that point even more strongly. And I have my own take on it, which adds pushy and manipulative politics of any kind as a RISK to science. The same “sale by urgency” which works for salesmen at the appliance store, works in science. Many of us – particularly those of us with historical perspective – saw this problem in climate science. Now, we see it in COVID and vaccines. We are being rushed into something, for some reason. The questions are WHAT and WHY.


I’m going to assume that most people reading this, have started to grasp enough of the basics of viruses and vaccines, and particularly the new mRNA and DNA vaccines, that they don’t need “the way things are supposed to work” explained to them. Indeed, if you go out, and absorb all the “mainstream” journalism on COVID – science sites – mainstream media – cable networks – your favorite non-conspiratorial “science guys” – fact checkers – explaining the way things are SUPPOSED TO WORK, you will be thoroughly and smartly educated by excellent science.

If you want, try this great link courtesy of Ethical Skeptic, one of my favorite “dissident scientists” out there, pulling us back from the current “woke Lysenkoism” we seem to be in.

See? Yeah, I’m a grade-A conspiracy theorist, because I told you to look at Snopes, and not some clickbait site saying these vaccines are injecting nanobots into you to turn you into something non-human.

The PROBLEM with the conspiracy theories on vaccination isn’t so much DIRECTION as it is MAGNITUDE. It’s all over-reach. Silly, perhaps well-intended, but self-discrediting overreach. Much of it is clickbait or psy-op. A lot of it is actually true – at some small level – often orders of magnitude less dramatic than the headline claims. I can talk to the consumers of such in terms they will understand, and I’m generally talking them DOWN and BACK to what are more scientifically grounded problems with the new vaccines. And there are some. Which is the POINT of this entire piece.

In this essay, I am now talking primarily to what might be called “vaccination normies”, who are – like me – normally rather trusting of vaccines, but perhaps feel like there’s something not quite right about the current situation. These are people who have SOME vaccine hesitancy, but are likewise leery of TRULY baseless skepticism of science.

I’m talking about the people who put “SCIENCE IS REAL” yard signs out in front of their houses. There is a side of me that likes that. However, there is a side of me that wants to put out a sign that drops LOVE IS LOVE (Pedo? No way!) and all the rest, and sticks to what I know about science from the inside:

  • SCIENCE IS REAL
  • SCIENTIFIC FRAUD IS REAL
  • SCIENTIFIC GREED IS REAL
  • SCIENTIFIC BIAS IS REAL
  • SCIENTIFIC ERROR IS REAL
  • SCIENTIFIC DECEPTION IS REAL
  • SCIENTIFIC SELF-DECEPTION IS REAL
  • SCIENCE IS REALLY MESSED UP
  • SCIENCE IS STILL BEAUTIFUL

You see what I’m sayin’? You want SCIENCE, you get the whole, lovely, crazy, smart, dumb, dysfunctional bimbo who thinks she can handle SOCIALISM, and ends up on some frat party lawn in a lab coat and a mini-skirt, throwing her shoes at strangers, demanding somebody take her home, and SHE’S NOT DRUNK.

Yeah. I knew that crazy, wonderful bitch.


Wolf’s Take on Coronavirus Vaccines

You can check out my posting history here to follow the chronology of my thinking on coronavirus vaccines, but I’ll try to recap toward my current thinking, and what seems to be wrong with them. I am going to lead you up to my last post on the vaccines, where I almost saw what I’m seeing now, plus a whole bunch of other stuff.

That post:


Branch Covidians – Seven Ways To See Through The Phony Pharmageddon of COVID-19

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 – …


The first news that really grabbed me was about Inovio – a DNA vaccine – a “Bill Gates” vaccine (almost all are, TBH) – and thus one of what I will refer to as genetic vaccines. Such vaccines are not supposed to work by modifying one’s genes or genome, despite the word genetic. They simply exploit cellular biochemical processes CLOSER to the genes, using the known biology of genetic expression. They dump DNA or messenger RNA (or a close facsimile thereof, to be more precise) into existing cellular processes, to “fool” the processes into creating – in the case of the current coronavirus vaccines – a stabilized form of the spike protein of the virus.

At the time, I noticed that these would be THE FIRST genetic vaccines being tested in or deployed successfully in humans. And this is where things get “iffy”. Just a little bit.

The next vaccine to get into the news in a big way was Moderna – an mRNA vaccine, again using a full and slightly stabilized spike protein as the antigen, but created in vivo via the mRNA genetic instructions thereof. While Moderna seemed to be successful in its first clinical trials, the side effects were noteworthy, frequent, and fairly significant – even compared to the notoriously “spicy”, arm-reddening-and-bicep-swelling, shingles vaccine, Shingrix. As one respected “pro-vax” scientist of my old acquaintance put it, they would have to kill him to give him the Moderna vaccine. He was definitely thinking the same thing I was thinking. Rush job, problems, keep looking.

My initial hopes quickly moved toward Novavax. Novavax is NOT an mRNA or DNA vaccine. It uses the same full stabilized spike protein strategy as the others, but it provides the spike protein AS spike protein, using a nifty little nanochemical “pincushion” to hold the spikes in an outwardly facing array, thus to engage receptors properly and at LOW DOSAGE. This is an excellent strategy that AVOIDS the unknowns of mRNA vaccines like Moderna, or DNA vaccines like Inovio or Russia’s Sputnik V.

The most significant risks of spike protein vaccines like Novavax are the risks of the spike protein itself, NOT of abusing the genetic processes to CREATE the spike protein in vivo, like Moderna. Indeed, Moderna scientists admitted in one of their first papers on their vaccine, that there ARE unknown potentials for long-term side effects with mRNA vaccines. Go find the paper – it’s there. They couch the admission in gentle and somewhat obscuring language, but the disclaimer is there. It has to be. They’re being honest.

mRNA vaccines in animals have not been uniformly free of side effects, to put it VERY kindly. We can argue about the severity of those side effects, and whether they extrapolate to humans, but I suppose we will find out now. The risks are there, and they tend to be long-term. So – in full disclosure – there are RISKS to mRNA vaccines. The older you are, the less the long-term risks matter, and conveniently, the higher the risks of COVID-19 itself. That’s a good thing. It means we only have to take the risks with those patients who can most likely afford them.

On the flip side, why the hell we want to take huge, unnecessary risks to vaccinate children is beyond me, but I’ll save those arguments for another essay. Or look at my LAST essay. Those arguments are, in part, subtle “history of vaccination” propositions that would bog us down right now.

In contrast, Novavax doesn’t take those risks. It’s a more conservative vaccine. This is why it jumped to the top of my list. An entire class of risks – the genetic processing ones – were automatically removed. As a “nothing can go wrong or I’m likely DEAD” vaccine recipient, I appreciated my better chances with Novavax.

BUT as a “real” scientist, I am not just swayed by THEORY – I love the results of EXPERIMENT. Thus, when Pfizer’s clinical trial results came out, I was IMPRESSED by the excellent antibody levels and the almost minimal side-effects. Far from being an arm-burner like Moderna, Pfizer was looking to be much milder on short-term side-effects, with stronger adverse effects being downright RARE. The large population of test subjects also implied that a recoveree LIKE ME was likely in the study by accident – and NO deaths or severe reactions occurred – definitely a GOOD SIGN for my case.

This not only bode well for lower likelihood of some kind of lethal short-term reaction due to my recoveree status – the smart scientific position would be that lower short-term risk very likely reflects lower long-term risk – and this supposition is completely absent ANY “knowing” causative reason to connect them.

Thus, Novavax and Pfizer were at the top of my list. Things were looking GOOD to take a vaccine, even if I didn’t get an explicit study on safety in recoverees.

And THEN reality started to hit.

Yes – when millions of doses of a vaccine go out, there are going to be deaths and injuries. We have a system in place – let’s be honest – which tries to HIDE the minority reports on vaccine adverse events, in order to keep buy-in on vaccine compliance. That doesn’t mean people should stop getting vaccines, any more than reports on horrible vehicle accidents OR the “hiding” of such accidents on the back pages of newspapers, mean that we should stop driving.

Nevertheless, my scientific curiosity was piqued. We DO have COVID vaccine problems now, and MORE than seemed to have been revealed by the vaccine trials.

WHY NOT DO SOMETHING ABOUT THEM?

I repeat. Differently. THERE IS NOTHING WRONG WITH BETTER VACCINES.

Taking stock of the many positives and negatives associated with THREE VACCINES which gained the most initial experience – Moderna, Pfizer, and Oxford/AstraZeneca – I noted three things, one from each.

Moderna – side effects sometimes REMARKABLY resembled COVID-19 itself – even up to SEVERITY.

Pfizer – nursing home patients were testing positive AFTER vaccination – some dying of COVID symptoms

AstraZeneca – hematological problems reminded me of another protein hemotoxin – snake venoms

I could go into deep details about these observations, but in TWO of the cases, it was VIDEOS where the “light-bulb” finally went on. So let’s look at some videos.


Moderna: Ben Stein’s vaccination experience

As I was listening to Ben, I was stunned. He was describing COVID-19 – at least from my perspective. This was not coincidence – this was SPIKE PROTEIN.

WHOA, NELLY!!!

Note that Ben is still “pro-vax” here – he’s just CAUTIONING people about REALITY.


Pfizer: Nursing Home CNA describes correlation of vaccination to later positive diagnosis and death

This man, a CNA in a nursing home, reported online what he had observed, amidst great personal anguish about “whistle-blowing”. He observed that he had protected his elderly patients for all of 2020, but when they finally got the Pfizer vaccine, many of them just started “testing positive” and DYING. He was NOT buying the management line that there was a super-spreader – if you listen to him, he’s fully contemptuous of the idea. He was CERTAIN it was the vaccine.

I agreed with this guy – a TRUSTED SCIENTIFIC REPORTER, in my opinion. His GUT was telling him that the chronology was one of correlation. He was very likely seeing in his mind a pattern in a delay over TIME, integrated over cases, that could only be explained by the vaccine itself. He was NOT accepting the management excuse of a “super-spreader” fortuitously infecting the vaccinated, to give that same result. THIS GUY is my kind of scientist. SKEPTICAL of ad hoc, contrived, politically correct explanations that don’t explain all the facts and observations in a clean, natural fashion.


AstraZeneca: Rare but serious clotting reactions are enough to evoke CONCERN from medical professionals

I think THESE DOCTORS in the following video represent my position extremely well – the problems with the AstraZeneca vaccine are RARE, but we KNOW there is a correlation, and it is our DUTY to stop and fix the problems, weighing in particular the relatively lower risks of COVID-19 itself in younger patients, where these events are occurring.

The difference between IGNORING the rare thrombocytopenia incidences and FIGURING THEM OUT is the difference between Stalinism and responsible popular government.

I truly admire these front line doctors for their SCIENTIFIC BALANCE. Frankly, I consider front line doctors to be scientists of the highest order, just like that CNA in the video above. PRACTICE is what matters – not DEGREES.

Now in this latter case, the AstraZeneca vaccine, I dragged in what I consider a very useful analogy to hemotoxic snake venoms, but I didn’t really see WHY this would be happening – until I found something that explains ALL of these problems.

I just didn’t realize I was holding an ACE.


The Macguffin – Reverse Transcription

In March of 2021, I reacquainted myself with a paper that I had noted when it came out, in December of 2020, but had not fully grasped the significance. The authors clearly knew that what they had found was a big deal, and worded the title appropriately, but even then, I don’t think they dared consider the possible deeper significance of their finding.

Nobody can FIRE ME from retirement, so I’m quite willing to say what needs to be said. Could it be wrong? Maybe. But if it’s RIGHT, there are issues that need to be dealt with. So let’s go there.

LINK: https://www.biorxiv.org/content/10.1101/2020.12.12.422516v1.full

ARCHIVE: https://archive.fo/XWC52

New Results Comments (42)

SARS-CoV-2 RNA reverse-transcribed and integrated into the human genome

Liguo Zhang, Alexsia Richards, Andrew Khalil, Emile Wogram, Haiting Ma, Richard A. Young, Rudolf Jaenisch
doi: https://doi.org/10.1101/2020.12.12.422516


I will refer to this paper at “the Jaenisch paper” – after the main author to whom correspondence is written – not because I don’t want to credit the fortunate and likely excellent first co-author Zhang in this instance, but because there is another paper I talk about all the time, dealing with masks, that I call “the Zhang paper“.

THAT one – the mask paper – in an embarrassingly good journal – is a piece of crap – some of the worst “political science” ever – designed to virtue signal to the CCP-DNC narrative of election-fraud-assisting masks, in utter contradiction to the very data presented by the authors.

The Jaenisch paper, in contrast, opens up a barn door that I am sure both industry and “in bed” government wants closed, Closed, CLOSED.

Stated very bluntly, the paper says that the virus behind COVID-19 actually “changes the genome” of victims – similarly to, though not exactly like, HIV.

You know – that OTHER disease for which Fauci was so interested in creating a vaccine.

And not only that – the COVID-19 virus does it enough to throw off those damn PCR tests that Kary Mullis warned us about for the exact same reason. In fact, the solution of that aspect of testing – the way “test-triggering fragments” just hung on and on and on in recoverees – is one of the BEAUTIES of the Jaenisch paper. The conclusions of the paper explain very neatly certain OBSERVATIONS and scientific conundrums that were first found by Korean scientists, who were very very persistent in proving that their COVID patients were NOT getting reinfected, as the fear-mongering American media “wanted”, but were still testing POSITIVE while being NON-INFECTIOUS.

Now we have a wonderful explanation. Excellent scientific work. THIS is why I signed up for science!

The THREE-TRILLION DOLLAR QUESTION that nobody wants to ask, however, is whether the genetic vaccines based on mRNA or DNA of the viral spike protein do the same thing – meaning get incorporated into the genomes of recipients. Well, do they?

Ever? Sometimes? Always? Or even just enough to make a difference?

It’s a great question! That deserves a CLOSE LOOK with MUCH SIDE-EYE.

I will say this. Even if these vaccines only get incorporated sometimes, that would make the “crazy people” yelling “OMG THESE CORONAVIRUS VACCINES ARE GENETIC MODIFICATION!” become suddenly – oddly – scandalously – CORRECT.

I find that incredibly ironic.

BUT WAIT – THERE’S MOAR. And then, there is EVEN MOAR STILL.


The Spike Must Flow

I had set the Jaenish paper aside in my mind in January 2021, as I was busy being pursued by the FBI as an “insurrectionist”, having wanted to see “fellow dissident scientist” Dr. Simone Gold speak at the Capitol Building on January 6, 2021. Rather luckily, I never found her, or realized where she was. Had I found her, I would have likely been arrested and all that nonsense, since she wandered, far too trustingly, into the interior of the Capitol building.

This old wolf, too wary to go into buildings – too old to play tug-of-war games – too injured to stand up to direct pepper spray – settled for singing the Star Spangled Banner at over 100 decibels with tens of thousands of patriots outside – which was an absolutely surreal experience.

But back to the story.

When I began seeing more and more vaccine problems by March of 2021, some of the possible answers seemed to point to the WHOLE SPIKE PROTEIN being the BAD ACTOR. The trouble was, I needed disease-producing levels of it. How might THAT be happening?

Look at Ben Stein. He was injected with only a small amount of COVID spike protein mRNA, but had disease like I did, when, in my case, the virus ran wild making BOTH spike protein AND more virus from it, in my cells.

The vaccine does NOT create any new virus. It does NOT have the full virus instructions. JUST the main one – the spike protein that provides a significant part of the viral shell.

Thus, the vaccine cannot create an EXPONENTIAL GROWTH of the spike protein, which the VIRUS does. The full virus creates more and more virus, meaning more and more spike protein, until something – immune response – shuts it all down.

The vaccine creates a few “fountains” of spike protein – basically “vaccine-infected” cells – but these get shut down as immunity builds. It never really gets out of control. Or at least, not normally.

So, for Ben Stein to have a powerful, disease-like experience, he needs cells that are cranking out far more spike protein than we would normally expect with the vaccine.

Well, if the INSTRUCTIONS for spike protein – in some people – got a bit upstream of just “slipping them into the print shop queue”, to where entire new print queues of spike protein and substantial, chimeric, problematic chunks thereof were being repeatedly ordered from DNA central operations, it would explain a whole lotta spike protein and associated chimeric junk being produced – more than anticipated.

And – I think I would be remiss if I didn’t consider the possibility that some of these bogus DNA instructions might be hard to shut down completely, thus providing an explanation of “long haulers” and “immunocompromised variant generators” beyond their known suffering of what can be rightly regarded as “simply” chronic damage from initial infection.

But let’s move on the to Pfizer nursing home case, and many other reported cases like it.

If we’re getting genetic incorporation of vaccine spike protein instructions at the DNA level by reverse transcription, like the Jaenish paper, perhaps in older individuals who are more susceptible to this problem, then it explains them testing positive later – and in some cases – if they can’t shut it off – DYING LATER.

Now – here is where KINETICS comes in. Kinetics is basically process flow rates. I talked about KINETICS in my LAST RANT on COVID-19, in which I began to put all this stuff together, but didn’t really put forth the totality of things until the comments section at the end of the post. I mentioned in the body of the post that the kinetics of viral interference didn’t seem to explain the nearly complete disappearance of flu while COVID was still significantly above herd immunity levels. It just felt to me that BOTH of these would shut down with greater similarity, if viral interference was the sole explanation. In that case, CDC lying to us about flu vaccine efficacy, understating the success to increase compliance, COMBINED with viral interference, provides a nicer (IMO) explanation of the observed kinetics.

Now, in the case of partial genetic incorporation, the kinetics of interest would be how fast the body shuts down spike protein production by cells without genetic incorporation, versus shutting down cells where there WAS genetic incorporation. If cells with significant production of spike protein due to genetic incorporation were not just sources of more spike protein and more symptoms, but also harder to shut down than “unincorporated” cells, and elderly people were increasingly subject to genetic incorporation with age, we might actually see the AGE-VACCINE DANGER relationship that is being seen in nursing homes, where the most elderly patients are at significantly greater and AGE-INCREASING risk from the mRNA vaccines – something we absolutely don’t want.

Are you starting to see why this explanation works for me?

Genetic incorporation of symptom-producing protein instructions by mRNA vaccines of the FULL SPIKE PROTEIN seems like a REAL WORKHORSE OF AN EXPLANATION.

And, if you’re following my reasoning, you can see that this can also explain the odd cases of thrombocytopenia in some younger patients getting the AstraZeneca vaccine.

In the AstraZeneca case, we would be seeing rare cases where spike protein production after genetic incorporation was just cranking away at levels reminiscent of hemotoxic envenomation by crotalids – or in English, snakebite, which is also (in certain snakes with certain proteins) characterized by thrombocytopenia.

I will tell you right now – there MAY be very similar cases in older patients – maybe not – but I suspect that such cases are less “systemically identifiable” in older patients where thrombosis is more “normal”, and will be more likely attributed to age and NOT the vaccine.

And here is the kicker. In all of these cases, because of the chimeric nature of the fragments noted in the Jaenisch paper, there is a certain RANDOMNESS which could be responsible for the random responses seen in different individuals and different vaccines, which by using significantly different mRNA vectors, may result in significantly different levels and exact circumstances of genetic incorporation in different individuals.

NOW – if it turns out that there IS genetic incorporation of vaccine-origin stabilized spike protein mRNA or DNA as genomic DNA, like the virus itself, then one of the first suspects for reverse transcriptase activity or induction thereof, would be the spike protein itself.

And THAT, my friends, opens up a REAL can of worms.


The Full Spike Protein Monty

Let me ask a really impertinent but really obvious question – something that Tucker Carlson is famous for.

Why are we vaccinating people with the WHOLE spike protein, or more precisely, stabilized analogs thereof?

OK – now I’m being a LAWYER here. I am asking questions to which I ALREADY know the answers, and in particular, the answers that Tony Fauci might give. Here is my argument on behalf of Fauci.

“We don’t really know EXACTLY where on the spike protein, might be the BEST place for antibodies to attack. Also, we don’t really have time to start guessing, when we can just use the whole thing. Most of the labs are modelling the whole molecule, and sharing data. It just makes sense that everybody sticks to the same model, so that any advances that one lab makes, can be quickly adopted by the other labs and researchers. If we begin using fragments of the spike protein, then results are going to be harder to interpret from lab to lab. There will be fragmentation of the science as well, and this will slow our response time tremendously. Comparison of results will be much more difficult. The timeline to a vaccine could be extended by months – even years. Maybe never……..”

See how that works? I would make a fantastic lying science bureaucrat – I know all the tricks already, because I used to negotiate compromises that result in the status quo in fake science in other ways.

Now – HERE is the superior counterargument that will LOSE because Tony Fauci is in control. For this argument, I’m a FRONT-LINE DOCTOR. Maybe I’m even Simone Gold, or one of the various doctors I followed back during the HCQ Wars.

“Yes, that’s all fine and good. But we are doctors, administering a VACCINE to patients. Adverse effects are real, and we want to minimize them. The spike protein is almost certainly the cause of much of the endothelial damage by this virus. Anything we can do to avert that damage is smart, including NOT using the full spike protein or analogs thereof. If we know the primary sites that antibodies need to attack, which we actually do, we can just use shorter peptide sequences or protein fragments constituting those sites. Modeling can make sure these fragments present the same, active, pre-fusion conformation. We can stabilize as needed to prevent immune enhancement, just like in the full spike protein. This shorter peptide approach has been successful in hepatitis vaccines. These peptides can be created quickly and formulated as vaccines in roughly the same time as the full protein. In fact, vaccine expert Winfried Stoecker has already done this, using the receptor binding domain of the spike protein, and creating a short peptide based on it. Since this technology is well-known, we don’t have to take any of the risks of messenger RNA or DNA technology. Nor do we have to use adenoviral vectors or new lipid nanodroplet technologies. Likewise, all of the advances in stabilizing pre-fusion conformation in the full spike protein can be used for the RBD peptide, so the risks of immune enhancement will be just as low. So, unless you can give us a reason to stick with the toxic spike protein, I’d say this is a no brainer.”

At least, that’s the way it looks to me.

Now, here are some interesting facts.

First, EVERYBODY is doing the full spike protein. The ONLY party that made a vaccine using less, was Prof. Stoecker, and he got in trouble for it, with the German government, because he wasn’t properly authorized, even though – well – normally he just does vaccine work and that’s that.

RBD_Regional_Antigenic_Vaccine_quadrupol-Mutante-3.png
RBD_Regional_Antigenic_Vaccine_quadrupol-Mutante-3.png

Second, you should note that – IF the spike protein has any reverse transcriptase (RT) activity, that activity would likely have been LOST by switching to a small peptide dropping most of the molecule.

Third, you should note that – by switching to a small peptide, there is no mRNA or DNA corresponding TO that peptide, so there is no chance it will be genetically incorporated.

By now, it is VERY clear to me, that the industry picked the vaccine technologies that it did, precisely because they were modern and untested, and they needed an “emergency” to get these technologies into use, in preparation for their big goal – actual gene therapy. But – AND LOGIC here – that does not preclude there being even MORE motivation here. The more I see this “event”, the more I see everybody getting bought in by SOME new aspect of the scam.

Using a more conservative approach would have been SAFER, but it would not have advanced the technologies that were groomed to be advanced. Even the Novavax protein-based vaccine, fairly conservative, tests the novel use of nanoparticles to assemble the pseudo-spike proteins into cell-infective starburst patterns. It, too, is full spike protein.

But again, THIS. Everybody is ALL about the full spike protein.

Let’s ask WHY.


A Feature – Not a Bug

Now – if the Jaenisch work is good – and I think it is – and if genetic incorporation of vaccine mRNA into genomic DNA also occurs – and I strongly suspect it does – and if the spike protein itself is responsible to at least SOME degree in causing genetic incorporation – which I also think is very likely – then I am of the opinion that Fauci knew exactly what he was doing in pushing mRNA and DNA vaccines that code for the full spike protein, and that he did so as a sneaky way to get a reverse transcription promoter into the human genome.

Why? I don’t really know. Not yet. But this whole thing just seems intentional in its ELEGANCE.

This is easily expressed in logical hacking terms. Fauci uploaded a stealthy FTP uploading tool into humanity’s genetic account. FIRST as a problem, with China’s help. THAN as a solution, with the industry’s help.

The idea of “uploading an uploader surreptitiously” is just elegant. It’s HACKING. Any person who ever had to “learn to code” has to admire it. And it’s doubly elegant by doing it TWICE.

Stated in biological terms:

Create a genetic vaccine for a same-same disease, both containing the genetic sequence of a reverse-transcription promoter, such as a reverse transcriptase, as a way of creating a persistent or at least consistently available presence of a reverse transcription activator in humans.

And the beauty of this scam, is that it’s “WHOOPS” played TWICE. VIRUS, then VACCINE.

Let’s enjoy it! Scenic route…….

FIRST the disease – OH, NO, LOOK WHAT BAT SOUP DID!

The ChiComs are masters of psychology on Americans. First they whip up the cultural WTF.

THEN they whip up the OTHER side of Americans saying “don’t hate on Asian cultural differences!”

THEN they pull the whole offering back, with everybody left high and dry on CCP zoonotic transfer garbage narratives, minus “bat soup”, but including pangolin “look squirrels”, when the REALITY is that humanized animal models are almost all that is actually used for this kind of viral research any more (thanks to Mary Morse for this fantastic point).

Wuhan lab. Put ALL your chips on it.

MASTERFUL MANIPULATION, and many American academic scientists fell for it like soldiers on leave in a brothel district.

THEN the cure – the vaccine – which uses the SAME genetics to get MOAR of the uploader installed in MOAR people.

And if they get caught….”OMG, DID WE DO THAT? WE JUST FOLLOWED THE SCIENCE AND THE DISEASE! FULL SPIKE PROTEIN FOR THE WIN! IT’S *** SCIENCE *** !!!”

This is masterful scammery, IMO.

https://youtu.be/Oza1j2_WqBk

Maybe even more than Kary Mullis realized.


Rand Paul Nails Fauci and Cuts to the Chase on Coronavirus Variants – Are the Vaccinated and Recovered Even Getting Reinfected or Sick?

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. …


Something is going on here, and it seems too purposeful to be mere incompetence.


SO – Does Wolf Take the Faucipox Vaccine?

Now – I’m gonna tell you – CRISPR-Cas9 vaccines are coming, and THOSE are straight-up genetic engineering. Save some ammunition for that fight. But right now, I think it’s worth bringing up some PRETTY TOUGH QUESTIONS about the current vaccines.

Simply stated – aren’t things with reverse transcription activity a RISK, like HIV, and why would we court that risk in a SOLUTION like a vaccine?

And what’s with all the LIES to keep people from noticing that the VACCINE causes positive tests in recipients, “because spike protein, sequences, PCR, and [COUGH] maybe a little incorporation”.



C’mon. This is so obvious now, it’s PAINFUL. CDC is not even looking foolish. They know this stuff isn’t the disease – it’s the vaccines. They’re LYING.

Sheesh. The whole thing is an outrage.

So. Am I going to take one of the current vaccines?

Not if I think there is a reverse transcription activator coded for in the mRNA or DNA, or even if it’s just in there as PROTEIN.

I’m quite good with my natural immunity, which sadly may ALREADY include some uploading of the uploader. I have no idea if I have any genetic incorporation from the virus already, but if I do, I know exactly where any future positive PCR test is coming from.

Anyway, thank you, Kary. You were right all along. They ABUSED your work.

W