What happens to those billions of NanoParticles you've become host to? [Revisited]
I revisited one of my first articles written two years ago to this day. Feel free to share it.
FYI: I use these grey blocks for my new comments so that you can distinguish them from the original article.
The original article is a poetic analogy of LNPs bouncing and wreaking havoc throughout our vascular system. I have since investigated all the avenues opened, and there is nothing to be ashamed of.
The only dimension that I didn't imagine then, also tied to the bolus - was cancer and genetic disorders, and I was far from having a solution to heal to propose to you.
For those of you who haven't read my Christmas article on Oxygen Therapy. I encourage you to do so.
Some of you might recall one of the most beautiful commercial ever, the colourful Sony advertising in my childhood’s neighbourhood in San Francisco. As you might recall, they let go 170,000 bouncing balls tumbling down the streets in a beautifully chaotic ballet of rubber balls of all colours.
During that poetic descent, balls bounce off rain gutters, car trunks, wooden tile roofs, lamp posts... Hitting mailboxes, running down trash cans, shaking newspaper racks… there’s no telling where they’d end up: stuck in a garage, in a garden, on a roof, who knows… The only thing certain is gravity was going to pull them down, a majority would end down at the Marina, and they will bang on a variety of objects along the way, solo or in the pack, in a wonderful haphazard choreography.
Current anti-COVID vaccines can be like bouncing balls in your body. Obviously Nanoparticles1 (LNP/Viral vectors) and spike proteins are far less poetic, but what they lack in poetry, they compensate in potential chaos and surprises. The domino effects they trigger sometimes can be disquieting and dramatic.
Read my latest article on the white clot syndrome as an example of Bolus severity:
Just as it’s impossible to explain why, how or when a particular bouncing ball opened up a mail box, or tipped over a trash can, it’s impossible to outline precisely the exact conditions which led to a particular adverse effect of these new lipid nanoparticle-based spike producing inoculations.
In the coming lines, I will try to outline commonalities, gravities and dynamics, that are factual and attempt to explain some of the mechanisms which probably cause illnesses and deaths following these vaccines. Trying to make sense out of this senselessness.
A crazy number of LNPs. An even crazier number of spike proteins.
The number of nanoparticles (NP) injected in a dose of these anti-COVID vaccines is utterly flabbergasting: up to 50 billion viral vectors for AstraZeneca, 40 billion LNPs for Moderna, and likely 10 for Pfizer. It’s not very clear how many intact messenger RNA are in each LNP , but even if we agree to only 1, and that each one produces 1000 spike protein, we are talking your body having to deal with a minimum 30 trillion pathogenic spike proteins2 in a few months time…
I was directionally right in terms of spike protein quantification and had missed (mea culpa) a study by Harvard Medical: Ogata et al. that detected a maximum level of around 3 trillion spikes at Day 5.
Many detractors have been saying I was always entrenched in the Bolus Theory. This proves I did consider Circulating Spike Theory seriously, but had to acknowledge the reality they were being neutralized by an even greater quantity of antibodies: 17,000 trillion antibodies.
Those are numbers way beyond very severe SARS-COV-2 infections: typically at infection peak between 1 and 100 billion virions, are present in the body.
What the medical and public health community hasn’t realised is that all the healthy cells that will be “infected”3 by these nanoparticles will eventually be destroyed by the immune system. When you take the Pfizer vaccine 3 times, you accept sacrificing up to 45 billion of your healthy cells… with AstraZeneca it’s 150 billion!
This is now acknowledged by people like Dr Robert Malone and Bret Weinstein but has been largely ignored by the vast majority of the medical community.
While many of these LNPs will transfect the same cell or will simply get destroyed before ever transfecting, for one reason or another, these numbers remain truly gigantic. And it’s no surprise that some people’s arms are painful - or others die quasi-instantly - post-vaccination as T-cells attack these spike-producing cells to start ridding the body of the infection mimicry.
Of course, these are supposedly intramuscular vaccines that were meant to stay in the muscle. Straight forward, no chaos, no unforeseen consequences: Theoretically, LNP fuses with muscle cell, mRNA is inserted, muscle cell’s intra-cellular machinery starts producing spike proteins, cells are identified by the immune systems as “compromised”, T-cells attack infected cells and the spike proteins are spilled into tissues and bloodstream to trigger antibody selection and production, antibodies neutralize and rid the spike protein. If the bouncing balls stay in the same place, then there’s no domino effect, nothing happens apart from muscle cells being destroyed and ultimately replaced. End of story.
So what’s that fuss about “bouncing balls” and chaos then?
Well, here’s the catch:
If you inject 10 billion nanoparticles into the muscle, how can you be sure it’s going to remain there? … You can’t!
Even if Sony had dumped 170,000 bouncing balls at a flat intersection in Pacific Heights, there’s a good chance many would have ended up going downhill. Planning is one thing, reality is another. Same with the vaccines.
My recent article on how - via sheer pressure differential - the vaccine would inevitably be directly pushed into the bloodstream proves how that statement was correct at the time.
There’s 2 different routes by which the LNP can escape the muscle, the blood stream and the lymphatic system. Both networks behave very differently, and the possible consequences of a leak are likely to be very different …
The Circulatory system is a closed-loop network circulating the blood throughout the body to bring nutrients, oxygen, and immune elements to organs, to filter out pathogens and dangerous or unwanted circulating material, and to refill on oxygen and unload carbon dioxide.
So the blood flows in a concentrated fashion to the heart, to the lungs, to the liver, and the spleen, not to mention, the brain and the reproductive system.
The Lymphatic system is an open-ended network; it’s the tissue drainage system as well as the immune system network linking lymph nodes, thymus, spleen, and bone marrow.
What will the vaccine Lipid NanoParticles end up doing outside the muscle?
Here’s the interesting bit. Just like we know for a fact that our bouncing balls bounce and are subject to gravity, we know for a fact that:
nano-particles deliver mRNA inside cells wherever they are located
transfected cells produce pathogenic spike proteins ☠️, release it and spread it
an immune reaction is stimulated - with specific Antibodies and T-cells - against both the spike protein, but also against transfected cells
millions - if not billions - of transfected cells will eventually be destroyed 💥💥
This shouldn’t surprise anyone, it’s the very purpose of these intramuscular products that are - at least in the short term - relatively innocuous if they remain in the muscle.
Multiple autopsies and biopsies have since then shown the presence of T-cell infiltrations, confirming that hypothesis:
- "Autopsy-based histopathological characterization of myocarditis after anti-SARS-CoV-2-vaccination" by Schwab et al
- "SARS-CoV-2 vaccination can elicit a CD8 T-cell dominant hepatitis" by Boettler et al
- "Autopsy findings in cases of fatal COVID-19 vaccine-induced myocarditis" by Hulscher et al
So, what happens if the LNPs get sidetracked?
When the producers of the Sony advertising decided to actually use real bouncing balls down the streets of San Francisco, they designed the experience not only to create a marvelous artistic experience but also to protect the pedestrians and the environment. The balls were chosen to avoid damaging Victorian houses and protection nets were installed to avoid harming people. They didn’t decide overnight to throw thousands of bouncing balls down a tourist-filled street like Lombard Street.
Lombard Street - San Francisco
A reckless production could cause damage and hurt many, either if a mass of balls descended on a few wondering tourists or just a few of them could cause a car accident to slip or a person to fall.
In the case of the vaccines, it seems “the balls have found their way down Lombard Street”. We are off-script here. It is clear that on many occasions, LNP are escaping the muscle with very serious consequences.
If LNPs are released away from the muscle, they are likely to reach and penetrate cells in three main areas:
endothelial walls in micro-vessels: where they are narrower, the probability of transfection is 440 times higher. In other words, the bouncing balls hit the walls more often when the street becomes narrower…
This confirms the fact that an extremely high concentration of LNPs is required to damage the endothelium as observed in the cases of white clot syndrome.
vital organ cells: just as blood vessels deliver nutrients to organs, they will likely deliver LNPs to the heart, liver, lungs… and even occasionally past the blood-brain-barrier into the brain
lymph nodes: the most likely organs down the lymphatic system, near the injection site, are the local lymph node which will naturally become receptacles of LNPs
That would cause major disruption downstream as large patches of interconnected cells get transfected, start producing spike protein, release large quantities of spike around them and are being attacked by T-cells:
in blood vessels, it will inevitably cause heavy inflammation, bleeding, clotting in the areas it is the densest, downstream necrosis, arterial calcification, and thrombosis: numerous strokes and thrombosis in adverse effects databases have demonstrated that to be true.
in organs like the heart, lungs, liver and ovaries, it will likely create a high degree of inflammation, cell death (apoptosis), and calcification ( pericardium for example causing heart attack): the high number of myo/pericarditis highlights this as a real possibility.
in lymph nodes, it could either interfere with the Lymph node function itself (B cells) as nanoparticle penetrate lymphatic nodules, or interfere with the immune system by transfecting immune cells contained in the Lymph node, with the risks of partial immune deficiency: The reappearance of dormant viruses such as shingles seem to point in that direction.
That preliminary classification was missing out on the extra reach of the bolus, notably in endothelial niches and the bone marrow, and the reality that stem cells could constitute a different type of danger because of their scaling properties. Here is the list of 12 different mechanisms of harm identified to date. The latest one, "Lack of Plasmin," explains white clot syndrome.
It seams reasonable to hypothesise that there are 2 ways these LNPs can end up in the wrong place:
accidentally by direct injection into a blood vessel (already addressed in another article “What could go wrong?”) or into the lymphatic system;
or naturally by progressively transiting through the muscle tissue and leaking into the blood stream, or into the lymphatic system.
What happens if, accidentally, the vaccine is injected intravenously?
The worse case scenario is certainly a direct intravenous injection because a concentrated dose naturally leads downstream to a concentrated transfection in a large area that it was never supposed to reach. That would lead to an extremely brutal reaction, a cytokine storm of epic proportion, major thrombosis, and most likely rapid death given the number of LNPs injected.
An indeed as early as March 2021, the Danish authorities have been recommending to use the aspiration technique to avoid such occurrences.
Saturating Lymph nodes with lipid nanoparticles can potentially lead to massive transfection of immune cells contained in this receptacle, and it can also lead to the transfection of Lymph node cells, inhibiting partly the functionality of these B-cell-producing organs and disrupting the immune cells present.
The more likely scenario is damage to the bone marrow (necrosis) or to the blood-bone marrow barrier (micro-perforation), both of which can cause immune depletion.
It's likely that the blood-bone marrow barrier perforation is temporary given the elevated presence of stem cells in the bone marrow ready for repair.
However, full necrosis of one or several bone marrows would inevitably considerably reduce the immune capacity of that individual, and given the large exposure of the bone marrows, that is likely to concern many of those who were unfortunate enough to receive an accidental IV.
What happens if LNPs progressively transition to the bloodstream?
We know from a comparative study of myocarditis in Norway and Denmark that avoiding direct injection by using the aspiration technique possibly reduced the numbers by at least 58%, but it didn’t cut it entirely. This seems to indicate that the nanoparticles are actually leaking out of muscle into the body as the blood and the lymph evacuate elements from the muscle tissue … in a more diffuse manner.
As NPs are injected into the muscle, it is only natural that some of it will eventually migrate to the blood stream like other elements in the tissue that are being evacuated via the blood. Multiple factors can play a role: It might vary based on permeability of blood vessel (elderly would be more at risk) or surface/volume factors (young males/ athletes could be more at risk).
Traditional vaccines never transfected cells in such quantities, hence a leak was never considered or identified as a problem to look into … it is nevertheless a key detail that was overlooked in the design of these vaccines.
Well, I was wrong again. Mea Culpa. It is quite obvious that traditional attenuated viruses, virus-like vaccines, and pseudo-viruses, are as dangerous when injected. Most vaccines can harm just as much. Only protein vaccines have a safer probability profile but they still can hurt. Here is the proof.
Depending on the total dose leaked and its distribution, concentrated or distributed, depending also on the quality of the product (Did poor quality actually save many lives?), and the repetition of the doses (1,2, 3 , up to 4 doses?), the scenarios can vary drastically:
First and foremost, the circulatory system - blood vessels - is at the frontline of these diffuse leaks of the vaccine into the blood. Endothelial walls are the principal surface the LNPs can transfect. The damage would be totally invisible and diffused but can last for months as vessel cell regeneration is a lengthy process.
Because all blood flows through them in a concentrated fashion, some organs would eventually be accumulating more hits than others, most noteworthy the heart and the liver. And indeed we are witnessing many cardiac and hepatic adverse effects.
I hadn't yet formulated endothelial exposure as being the greatest driver of organ exposure. See below article for more.
Some organs won’t regenerate like the heart (myocarditis isn’t mild, once myocytes have been destroyed, you can’t regenerate them) or will take longer like endothelial cells. So you can have a capacitor effect whereby each injection weakens the organ, or makes the situation worse, increases the inflammations, to a point it snaps: causing a blood clot, a stroke or a heart attack.
“Vaccine Induced Immune Thrombotic Thrombocytopenia Causing a Severe Form of Cerebral Venous Thrombosis With High Fatality Rate: A Case Series”
As many of you know, the risk of myocarditis increases after the second shot. One hypothesis is that LNPs migrate progressively to the bloodstream, meaning that they wouldn’t transfect in concentrated matter, but diffuse throughout the body. This is consistent with the elevated D-dimers found in many patients post-vaccination.
Beyond the fact that the vaccines are utterly ineffective, the mechanisms by which they are harming people is not a complicated as we think. The Danes have apparently reduced the risk 60% by enforcing the aspiration technique. One wonders what the other public health agencies have been doing since! Another CDC alert highlighted leaky blood vessels, which was a problem. Again, admitting the risk caused by these products going intravenous. One wonders how anyone knowing that would continue to vaccinate billions. How can any of the authorities be certain these products won’t leak? They can’t. They never could. It was excusable not to understand the implication of transfection. It is not excusable to avoid looking at the reality in the face for over a year. And they will soon stand trial for that. I wouldn’t want to be their lawyers…
I hope that was an interesting read. Feel free to share the “Covid Myth Buster Series”.
Apologies for being so long again… Here’s the lovely and soothing Sony video of bouncing ball down my childhood’s SFO hills.
Two years down the road, the Bolus Theory has never been falsified; better, it is more robust and more consistent today, spanning other vaccines and other cytotoxic products like venom. In my career as a consultant, shaky theories never held long, and certainly don't grow.
I hope those of you who hadn't read this article previously enjoyed it. Feel free to share it. A big thanks to those who are supporting my family and my work financially. Given my personal financial difficulties, I perfectly understand many cannot contribute; please help out by sharing the articles and learning as much as you can about the Bolus Theory to be able to argue around you. For those who can, I hope you'll consider helping me to pursue my effort.
I thank you all from the bottom of my heart for taking the time to read my work.
A big hug from cloudy Paris. Marc
for simplicity purposes, I am using the same term, LNP, for both Lipid NanoParticle and Viral Vectors, which are very different in nature, but both end up converting the cell in a spike factory and will also trigger the destruction of transfected cells by the immune system.
AstraZeneca could be as high as 150 trillion spike protein produced if not more
The right term is “transfected” for mRNA, and “infected” for viral vectors.