EXCLUSIVE: Daily Beagle Sniffs Out Blood Clot Cause
EXCLUSIVE: Daily Beagle Sniffs Out Blood Clot Cause
We finally cracked the end-to-end mechanism boys and girls!
It has been over two years, and The Daily Beagle has gone over everything from the EMA leak documents on mRNA instability to the over 3000 pages of Fauci FOIA documents, we have not stopped searching for the truth, no matter how burdensome or tedious. Consequently if you feel like fiancially supporting our hard work (that often involves staying up at 3am and beyond), please do so here:
That said, The Daily Beagle originally was of the common view that the spike proteins were somehow responsible for the clotting, given this was an often repeated claim by a number of field experts, with the mechanism simply undiscovered. However, in truth, no-one knew the precise and exact causes.
From a cardiovascular aspect it didn’t make much sense as thrombocytes (the cells that form clots) essentially only cling to other thrombocytes, and the SARS-CoV-2 spike protein does not have any similarities to thrombocyte clotting behaviour to trigger this behaviour.
It was overwhelmingly evident the shots do cause clotting, with the FDA forced to admit as much with the Pfizer shot, given the rise in blood clot cases and evidence of long, fibrin-like clots found by morticians, but the precise mechanism was a mystery. Until now.
Putting Together The Pieces Of The Puzzle
Our first port of call to solving this mystery is the BMJ’s (British Medical Journal) coverage of the EMA leak documents. In their assessment of the documents, the BMJ raised an issue not directly mentioned in the documents: Biodistribution:
In a rapid response posted on bmj.com, JW Ulm, a gene therapy specialist who has published on tissue targeting of therapeutic vectors,13 raised concerns about the biodistribution of LNPs: “At present, relatively little has been reported on the tissue localisation of the LNPs used to encase the SARS-CoV-2 spike protein-encoding messenger RNA, and it is vital to have more specific information on precisely where the liposomal nanoparticles are going after injection.”14
Don’t worry if you didn’t bring your medical textbooks. LNPs stands for ‘liposomal nanoparticles’, and for simplicity, it is the tool used to deliver mRNA into cells.
Biodistribution (bio, Greek for ‘life’, like in ‘biography’ and ‘biology’) is how something distributes throughout the body of a lifeform (this could be a human body or an animal body).
JW Ulm’s point here is Pfizer failed to provide evidence — at the time of the BMJ’s investigation into mRNA instability — of where in the body LNPs go, and posits this consists of a crucial safety risk. Remember: safety has to be proven, and if they haven’t shown evidence knowing where the LNPs go, it is a fundamental risk.
Not knowing where it goes could mean that, instead of ‘localising’ in the arm, it ends up in large quantities somewhere else, such as the liver.
Pfizer of course knew where in the body the LNPs went, but they kept the information secret until a recent Judicial Watch FOIA lawsuit forced the FDA to turn over the Pfizer evidence to the public. Imagine having to sue a so-called ‘health regulator’ to force them to tell the truth and be transparent on health and safety.
The Judicial Watch Lawsuit
In the lawsuit “JW v HHS FDA Pfizer BioNTech Vaccine”, a 468 page document was crowbarred out of the iron grip of the FDA revealing details on unpublished Pfizer animal studies.
The documents were not made public until a year after the EMA leak documents (March 21st 2022, to be exact). The evidence of why Pfizer would want to keep this hidden is it provides damning proof on the mechanism involved.
If it’s been sitting around for about a year, you’re probably asking…
Why Wasn’t The Mechanism Uncovered Sooner?
Judicial Watch are primarily a legal transparency group, so they won’t have assessed it from a medical standpoint, and many competent medical experts are far too busy with their usual practice to have time to read.
Even if medical experts did read the documents, their knowledge is classically specialist, a silo, so they may have read it but not realised the implications.
Putting the pieces together requires an understanding of LNPs, biodistribution, cardiovascular systems, clotting, the history of adverse events with the shots, access to said documents, and a willingness to put it all together.
The Daily Beagle didn’t notice sooner because there is such a landslide of information we haven’t finished processing, all whilst the vaccine industry throws out even more insane ideas like weaponising mosquitoes.
For example, the 3000 pages in the Fauci FOIA is roughly equal to reading 2 and a half War and Peace novels (1,200 pages per novel). We also compiled over 800 studies, case reports and more on adverse effects.
We’ve also still got this ungodly Pfizer FOIA mess to go through at some point (some are several thousand pages long. Per ZIP folder) whilst also maintaining a news reporting Substack. The Daily Beagle is literally a full time job and then some:
So What Is The Mechanism?
Please use this document from Judicial Watch’s FOIA lawsuit as reference. As it’s not possible to link directly to specific pages, page numbers (as numbered by the PDF tool, and not the document itself) will be given as references for the various statements and screenshots.
On page 19, the Pfizer animal trial admits the LNPs escape from the injection site and enter the bloodstream — exactly as JW Ulm had feared — and then distributes to the liver:
They insist there was ‘no evidence of liver injury’, but the rats were only alive for 3 weeks (‘recovery period of 3 weeks’), which is not long enough to observe long term harms, and even with that misleading term, the paper keeps using caveats by using the phrase ‘partial recovery’ or ‘partially recovered’ and similarly to indicate actually they hadn’t recovered:
This shows, no, the rats did not in-fact recover during the 3 week recovery period. We then see that the LNPs were ending up in lymph nodes, bone marrow, spleen, and crucially, the liver. Once again, the word ‘partially’ is thrown out to skirt around the issue of failed recovery:
The term for a liver inflammation is ‘hepatitis’ (from the Greek word ‘hepar’ meaning ‘liver’). There are numerous peer-reviewed papers indicating an auto-immune associated hepatitis with SARS-CoV-2 shots: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11.
What Liver Injury Has To Do With Clotting
Now, you’re probably thinking ‘that’s interesting, but what does liver injury have to do with blood clots in the cardiovascular system?’.
Ironically, the Pfizer animal trial answers this question, damning the company in the process that they knew.
Notice it says vacuolation of hepatocytes “were present for all BNT162b2 (V8)-dosed animals”. Not some. All. BNT162b2 is the BioNTech shot manufactured for Pfizer.
Hepatocytes are cells found in the liver. Vacuolation is a fancy word for saying the cells essentially had ‘holes’ in them. This isn’t a good sign as “vacuolation in hepatocyte nuclei is a marker of senescence” (senescence means aging, as in it is a bad sign).
Why is this detail crucial? Hepatocytes are involved in manufacturing serum albumin, fibrinogen, and the prothrombin group of clotting factors.
They trigger clotting.
And we can prove Pfizer knew this because they state as much in the animal studies:
See that? About 17 days in (2 weeks and 3 days), there’s a giant increase is fibrinogen, up by 2.49 times. And what is the descriptor for fibrinogen?
Fibrinogen (factor I) is a glycoprotein complex, produced in the liver, that circulates in the blood of all vertebrates. During tissue and vascular injury, it is converted enzymatically by thrombin to fibrin and then to a fibrin-based blood clot. Fibrin clots function primarily to occlude blood vessels to stop bleeding. Fibrin also binds and reduces the activity of thrombin.
It is a protein that causes fibrin-based blood clots. It details end-to-end the cause of the giant fibrin based blood clots in people’s cardiovascular systems. Exactly the same kind being reported by the morticians. They were right. And this is the slam dunk evidence that proves it.
LNPs leave the injection site, they accumulate in the liver, cause damage to the hepatocytes (liver cells), triggering both hepatitis (liver inflammation) and causing the liver to produce fibrinogen in response to the damage, causing massive internal clotting.
It is the slam dunk evidence the shots are killing people.
They must be halted immediately.
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Update: Jessica Rose PhD has requested the inclusion of her articles which covers spike protein related blood clotting in a more technical depth, which you can view here:
Spike S1, heparin and the coagulation cascade
Feel free to leave a comment below:
Underdog, I invite you to check out an interesting theory on the mechanism of the vaxx injuries at this stack: https://covidmythbuster.substack.com/p/the-cytotoxic-bolus-theory-on-the
He claims the spike protein is a non factor, and the injury is a result of the injection itself creating a clump of LNP's that injure the lining of the vascular system (leading to clots, strokes, aneurysms, heart attacks etc). These injuries are repeated across all vaccines types, the only difference with C19 being the largely quantity and high temporal concentration of vaxxes making the injuries more noticeable to all.
I am a simple layman but find his hypothesis very plausible.
Your idea makes more sense than most of the clotting schemes that I have seen presented.
I assume that you have also read about these proposed mechanisms:
https://open.substack.com/pub/amidwesterndoctor/p/how-do-vaccines-cause-sudden-death?
Search down the post for the section “Why Do the Spike Protein Vaccines Cause Blood Clotting?”
Also:
https://open.substack.com/pub/amidwesterndoctor/p/what-is-causing-the-died-suddenly?
AMD regularly responds to comments. I will post your article there. He will likely be interested in your research.