Embalmer Survey: KILLERS “CALAMARI” of BLOOD CLOTS raise after mRNA Covid Vaccination linked to Toxic Spike-Fibrin interactions of SARS-Cov-2 BioWeapon
By Fabio Giuseppe Carlo Carisio
I have published many explosive investigations on the dangerousness of mRNA genetic serums improperly called Covid Vaccines even though they are actually Gene Therapies.
This statement was included in the official report of the Slovak Commissioner appointed by Prime Minister Rober Fico to shed light on the efficacy and dangerousness of vaccines and the Attorney General of Slovakia is investigating it, the only country in the European Union to have opened investigations similar to those already started in the USA by 5 attorneys general and in Australia.
But this article is certainly one of the most explosive but perhaps even less than the next one for which we are collecting adequate arguments.
Below you can read the articles of two of the most important researchers in the world focused on the dangerousness of new biotechnology Covid vaccines with messenger RNA: Nicholas Hulsher, American epidemiologist, and Jessica Rose, Canadian bioimmunologist.
Their scientific texts published with a popular slant on their Substack are based on two important researches.
Two Explosive Study on SARS-Cov-2 Bioweapon and Covid mRNA Vaccines Dangers
Rose’s on a study published in the prestigious specialized journal ACS Pharmacology & Translational Science with an eloquent title: Spike Protein–Fibrinogen Interaction: A Novel Immune Evasion Strategy of SARS-CoV-2?
It correlates the toxic Spike protein of SARS-Cov-2, created in the laboratory we add after 90 investigations on the subject, in the dangerous interaction with fibrinogen, a protein synthesized in the liver that plays an essential role in blood clotting processes.
I quote the topic questions that Jessica Rose wrote:
«Fibrin[ogen] binds to the SARS-CoV-2 spike protein → blood clots form → systemic thrombo-inflammation and neuropathology. So what about the shot spike? Isn’t it more than fair to assume this same pathology since the shot spike was mimicked after the SARS-2 spike? And furthermore, if SARS-2 was indeed made in a lab – as I and many others suspect it was – then how could it ever be possible to believe that the engineers didn’t know and/or anticipate these downsides (binding fibrin) to using the spike protein as the immune system activator?»
«And why were the bioinformatics studies done (ie: to identify peptides in the NTD that resemble human proteins involved in various biological processes) AFTER the design and forced roll-out of injectables that incidentally used this very same spike as a template for in-host mass-production of synthetic spike?»
Monumental research among embalmers on “Calamari” of Blood Clots in Vaccinated People
Hulsher’s study is based infact on a monumental research among embalmers from all over the world who found the presence of white blood clots of fibrin (another name for the same protein) in the bodies of people vaccinated with Covid mRNA or mDNA gene serums,
If the researchers who discovered the role of fibrinogens in SARS-Cov-2 limit themselves to denouncing the danger for potential autoimmune damage resulting from the Covid-19 virus, the analysis of patients’ blood gives an explanation for the millions of cases of thrombosis that have seriously damaged vaccinated people, killing many of them.
It should be remembered that while the Covid-19 infection, if treated well and promptly with everyday drugs (anti-inflammatories, antivirals, antibiotics or herbal drugs), records a very temporary and fleeting presence of toxic Spike.
The Persistent Toxic Spike in Covid Vaccines
The toxic Spike of mRNA genetic serums, based on the same protein as the laboratory-enhanced virus with HIV, can persist in the blood for up to 2 years, as demonstrated by the exceptional investigation of theItalian bioimmunologist Mauro Mantovani (member of the British Society for Immunology) who was also the first to discover the presence of the “double proline” in Covid vaccines, which is crucial for this persistence.
This long permanence of the Toxic Spike in circulation in the body of vaccinated people has also been certified by the study of an Oxford researcher, the Japanese Akiko Iwasaki, professor of Immunology at the Yale University School of Medicine.
This is why it is not surprising that the research of the embalmers mentioned by Hulsher detects a toxic process of blood clots but becomes of crucial importance in detecting the role of fibrin that the study cited by Rose and the others conducted by the same Canadian bioimmunologist on blood clots identify as responsible for a potentially lethal interaction for the human immune system.
I have tried to explain very complex issues in a very simple way and therefore I will probably have made some technical inaccuracies. Therefore I invite you to read the two exceptional scientific articles.
The Graphene Oxide in Calamari of Blood Clots
I also remember that some Italian doctors, thanks to the help of an expert academic professor of electronic microscopy, have identified in these clamari of blood clots the presence of chemical substances similar to graphene oxide, a synthetic material potentially very dangerous in biomedical use, as we have demonstrated in a dossier of about ten investigations on the subject, which is expressly cited in Moderna’s patents on the Covid Spikevax vaccine.
So the toxic Spike enhanced in the laboratory, the interaction with fibrin and graphene oxide, the insertion of the double proline and the diabolical molecule (methylpseudouridine) have created a mix that makes the Covid vaccines real bioweapon of experimentation and mass depopulation.
Unfortunately in Italy they are still insistently recommended by the Meloni Government and in particular by the Ministry of Health as it is led by Professor Orazio Schillaci, former rector of the University of Rome Tor Vergata, intrigued both with the Big Pharma producers of mRNA gene serums but also with the research of Bill Gates and the Pentagon’s Darpa agency.
Read the embalsamer survey below…
Fabio Giuseppe Carlo Carisio
director of Gospa News
investigative journalist since 1991
VT columnist since 2019
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Worldwide Embalmer Survey Reveals Striking Rise in White Fibrous Clots Following COVID-19 Vaccination
ByNicolas Hulscher, MPH – originally published on his Substack Focal Points Courageous Discourse
All links to previous Gospa News articles have been added in the aftermath
Retired U.S. Air Force Major Thomas Haviland joined epidemiologist Nicolas Hulscher to present findings from two large-scale investigations into post-vaccine clotting abnormalities—one focused on the deceased, the other on the living.
The latest Worldwide Embalmer White Fibrous Clot Survey—a multi-year investigation documenting the sudden and widespread appearance of anomalous white fibrous clots in the deceased—draws from the testimony of embalmers around the globe who began observing these structures after the rollout of COVID-19 mRNA injections.
The companion People’s Blood Clot Survey gathers more than 1,400 self-reported and observed clotting cases from individuals across 40 countries, offering further insight into delayed clotting complications following vaccination.
2024 Worldwide Embalmer Blood Clot Survey
Respondents: 301 embalmers from multiple countries
Key Results:
- 83% (250 embalmers) reported seeing large, white, fibrous clots in corpses during 2024—up from 73% in 2023.
- These clots were found in an average of 27.5% of all embalmed bodies, a rise from 20% in the previous year.
- Embalmers stated they had never observed these clots before 2021, coinciding with the introduction of COVID-19 vaccines.
- 78% also reported seeing signs of microclotting—described as “dirty blood” or “coffee grounds”—in about 22% of cases, compared to less than 5% before 2020.
- Most embalmers acknowledged that their professional associations have never addressed this issue, despite high visibility in the field.
2024 People’s Blood Clot Survey
Respondents: 1,425 individuals from over 40 countries
Purpose: To gather self-reported or observed blood clotting events since 2020
Key Results:
- 1,294 individuals (91%) with clotting issues had received at least one COVID-19 vaccine dose.
- Only 79 clotting cases were reported in 2020 (pre-vaccine), compared to over 500 per year in 2021–2024.
- 26% of clotting cases occurred six months to over a year after injection—supporting theories of delayed-onset clot development.
- Most common clot locations: legs, lungs, brain, and heart—exactly matching CDC’s V-safe “free text” field analysis.
- 257 individuals required surgical removal of clots; 242 individuals died from clot-related complications.
Broader Implications & Suppression
- Major Haviland submitted his survey findings each year to the FDA, CDC, and NIH—without any response.
- Associations in the UK and other nations refused to participate despite having codes of ethics requiring investigation of unusual post-mortem findings.
- Vascular surgeons and cath lab workers, though reportedly encountering similar clots in living patients, have remained silent—many citing fear of professional repercussions.
Analysis by Greg Harrison’s team and Dr. Kevin McCairn revealed that these clots:
- Are composed of misfolded proteins (amyloids)—not blood.
- Contain abnormal fibrinogen ratios and high phosphorus, not typical of thrombi.
- Tested positive for prion seeding using RT-QuIC, raising concerns of infectious protein activity.
As Tom Haviland prepares to present to the Tennessee Funeral Directors Association in June 2025, the data continues to point to a persistent, under-investigated, and potentially catastrophic post-vaccine pathology. Despite the reluctance of institutional authorities to act, independent researchers and embalmers worldwide are stepping up to document what many believe is one of the most urgent and unaddressed medical phenomena of our time.
Nicolas Hulscher, MPH – originally published on his Substack Focal Points Courageous Discourse
Epidemiologist and Foundation Administrator, McCullough Foundation
Composition of the Clots
In this eye-opening interview, I sit down with embalmer Richard Hirschman and industrial chemist Greg Harrison to investigate the emergence of large, white fibrous clots in deceased individuals who received COVID-19 mRNA injections.
Hirschman, a seasoned embalmer with over 20 years of experience, first began noticing these unusual white, rubbery clots in early 2021. Found in both veins and arteries—a rarity in embalming practice—their frequency and composition were unlike anything he had encountered in two decades of work.
Explosive Survey! Monstrous “Calamari” Clots of Blood inside Vaccinated Dead after mRNA Shots
To better understand what they were made of, he partnered with Greg Harrison, an industrial organic chemist with deep expertise in polymer analysis. Harrison subjected the clots to rigorous biochemical testing using techniques like ICP-MS, HPLC, Raman spectroscopy, and RT-QuIC.
What they uncovered is nothing short of shocking: these are not ordinary post-mortem clots. The structures are composed of misfolded fibrin proteins with amyloid characteristics—including signs of infectious amyloid behavior, capable of triggering misfolding in other proteins. These findings raise grave concerns about a novel, systemic disease process that may be silently affecting millions:
What’s Inside These Clots?
Not Normal Clots:
These are not “chicken fat clots” or ordinary post-mortem artifacts. Richard Hirschman, who has embalmed thousands of bodies, began finding these anomalies only after the COVID-19 mRNA injection rollout in 2021 — not during the height of the COVID pandemic in 2020.
- The clots are rubbery, fibrous, and white, often stretching several inches and appearing in both arteries and veins — which is highly unusual.
- Traditional blood clots are soft, jelly-like, and typically limited to veins. These new clots are durable, rope-like, and difficult to break down — even with conventional embalming procedures.
- Hirschman reports seeing these clots in 30–50% of all bodies he embalms, a rate that fluctuates but remains persistently high — and many other embalmers are now reporting the same.
READ MORE BELOW
Clot Composition (ICP-MS, HPLC, and Amino Acid Profiling):
Greg Harrison’s team subjected the clots to a battery of analytical techniques, revealing profoundly abnormal chemistry:
SARS-2 Spike Protein–Fibrinogen Interaction to block antibody effectiveness
by Jessica Rose – originally publishe on her Substack
Jessica Rose has a BSc. in Applied Mathematics, an MSc. in Immunology, a PhD in Computational Biology and a two Post Docs in Molecular Biology and Biochemistry.
A paper was published in ACS Pharmacology & Translational Science entitled: “Spike Protein–Fibrinogen Interaction: A Novel Immune Evasion Strategy of SARS-CoV-2?” on March 19, 2025.¹
The paper explains why binding of human fibrinogen to the SARS-2 spike protein blocks neutralizing antibody responses by binding a specific region of the N-terminal domain (NTD) of the spike protein.
The NTD is more conserved amino acid-wise than the receptor-binding domain (RBD), and so it can mutate less effectively away from antibodies to evade the immune responses, technically. This is why we get variants of SARS-2 by the way: the RBD is highly mutable precisely for this reason – to make itself less “bindy” for the established antibodies to ensure its prolonged survival. But in more conservative areas, this is less likely to happen. Brilliant these viruses.
Think of it like this. Let’s also say that you’re like the spike protein and someone else is like an antibody. Sometimes when you first meet someone there is a strong initial attraction. Let’s assume that is the case in this example. Let’s also let the RBD be Trump talk, and let the NTD be food talk. So when you – as spike – talk Trump, you’re engaging your RBD. When you talk food, you’re engaging your NTD.
Over time, you might find yourself wanting to get away from this antibody person. Maybe they wear too much AXE. Maybe they like Kamala. So you start talking more and more about Trump to repel them. It is inevitable that the attraction will wane as the by-product of your words. Like perceptual amino acid changes (or mutations) to make yourself simply repulsive to the other person, the bond is severed: the more you speak, the less strong the bond becomes. Soon enough, they’re running on their little antibody legs for the hills.
The NTD would be more like trying to dissolve this bond based on food: we all need food and like to talk about it so it’s less likely this will be a bond-breaker. But then again, we don’t like the same food. If you start talking about stinky cheese, you might just repel antibody person, especially if there’s another someone named Fabiogen waiting on the sidelines who loves stinky cheese. I think this comparison got off track. I think you guys get it.
The Sudy on Fibrinogen interactions with Spike Protein
Back to the paper.
Here is what they write in their abstract:
“The host protein fibrinogen has been found to interact with the N-terminal domain (NTD) of the spike protein in SARS-CoV-2. However, the evolutionary benefit of this binding to the virus still remains unclear. Herein, we put forward with rationale and supporting evidence that the binding of fibrinogen to its more conserved NTD is an immune evasion strategy adopted by the virus to outsmart the NTD targeted neutralizing antibodies”.
Now this is a very interesting finding from the point of view of the mutability of the NTD, but the thing that bothers me about it is the link to clotting via fibrin. Why the hell would the spike protein bind fibrinogen and not only bind it, but strongly, and to the disadvantage of immune system functioning? I mean, the authors do suggest that it could be an evolved escape mechanism learned by the virus as part of survival to block/avoid antibody binding/removal, but why do I feel like that’s completely wrong? I feel quite certain that spike person always loved stinky cheese and just liked Fabiogen more from the start because spike person knew that Fabiogen also liked stinky cheese. Somehow. 😀
As the authors describe, fibrinogen is the precursor to fibrin which is really important in terms of the clotting pathway and its proper functioning. Fibrinogen levels correlate with SARS-associated disease severity and also to predict post-COVID-19 cognitive deficits. To me, this is old news, but papers like this one confirm what only a handful of us have been predicting for years.
I have written extensively on the relationship between spike and clotting factors for years.
by Jessica Rose – originally publishe on her Substack Unacceptable Jessica
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All of the articles written by Jessica Rose on this subject matter
Is SARS-nCoV-2-associated systemic micro-clotting due to spike protein-induced hemolysis resulting in amyloid plaque formation?
