Part 1 is here: clot.html.
During an interview with CHD, Ana Maria Mihalcea also claimed that the calamari clots contained spider silk protein. She said: "Clifford Carnicom and I have got the deceased clots from Richard Hirschman, we got a clot from a living vaccine injured person, and from an unvaccinated individual. And what we looked at is clearly this rubber-like material that we know about. And we did by mircoscopy, and we found the same filaments that we see in the blood, absolutely the same stuff, okay. And then we did near-infrared spectroscopy and found that these things have a polyins, which is polyethylene alcohol, polyvinyl alcohol, which is plastic, and polyamide, which is silk, nylon, or Kevlar. And specifically, you know, Kevin Kerningham, Dr. Kerningham [meant McKernan] found the genes of DNA of spidroins of spider silk. That's the strongest military-grade material that they have made. And so we found these in the clots." [https://x.com/ChildrensHD/status/1845970364993798325, time 41:40]
However McKernan did not actually find a spidroin protein in the Pfizer vaccine sequence, but "spidroin" was a nickname he gave for the long open reading frame he found on the reverse strand of the Pfizer sequence. When he searched for the reverse ORF on UniProt BLAST using extremely liberal settings, the closest match happened to be a protein that was annotated as a spidroin by chance, even though it was an extremely distant match that had only about 25% identity, and it wasn't have returned as a hit when he ran regular BLAST with the default settings: [https://anandamide.substack.com/p/spider-webs-in-the-pfizer-closet]
The spidroin protein sequence was likely misannotated, and it was removed from UniProt in June 2024, so it is no longer even returned as a result if you do a BLAST match for the reverse ORF. But before it had been removed, I downloaded the Pfizer plasmid sequence that McKernan uploaded to GenBank, and I picked the longest ORF on the reverse strand:
$ curl 'https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi?db=nuccore&rettype=fasta&id=OR134577'>pfizerplasmid.fa
$ r=$(seqkit seq -rp pfizerplasmid.fa|seqkit seq -s);for x in $r ${r:1} ${r:2};do sed 's/.../& /g'<<<$x|grep -Po 'ATG.*?(?=(TAA|TAG|TGA))'|tr -d \ ;done|awk '{print">"NR}1'|seqkit translate|seqkit sort -lr|seqkit head -n1|seqkit seq -s
MQYQLESSCVVQFHALQHGLRIVLVELAAAATATTALQAATAAGHATQHDCDHHDGNQSGDKAQPDVPGPLDVLLVLPQFLQVDQALVQILGHLVQPVDLFLDVHDAGIDSADIAQVHVGACVVLKVLVQFLFEAVQLGLQRVVHGIVHNADHDVAVARHEGVVGGDDLGLVEVPLCHEPMGAVGHEHAFSRKVGFAVVADGWSGGEILLLSGHICHVQKHHAVRGRLREAHQVVALAAKVHSLALAQHTLRHLGGGQIGRGSNLGGSDQLLGHVCLEALQSACDQSVDLHLGLRRVQSAQDIVQHRADGAELGGQLLDQGVQCLGIVVDHVLQLSQGACCAAQAVLDLADGAVELVGDQLLVLVQHILGHSDAVEPVGHLHSKGDLQSGACSKCPAACDCAGQQGRCVLGDHLIGQQRRQHCQSVKLLGANQIPGGNVAQTIAILLDEAGVGQCHFVEQQVLDEAPLAGLARIGQNLAEIEAAEVLDRRGLVDLLHLGEHLLGVLVLFHGDPCQGSFQLGAEAAVLQQQVGALGGIAADVHGAVHAGLGHGHRQDLCGHADGEVGGDSDRVVGVGHAVLGAQRHCVGNDALAGHASGSPVALCLCLVAGADSSADGDVALVAIVHVLGSDQTAGSGLKHIAAGGVHPPCRCQLIGVNGHGHFGTVHALVQHCHLIAGVGARGDHRHSAEAARGDVQDFQCLGISNGVCGIGDIPAKLLEWQELLVALCQHAGAGQAVEVEVHAFVLHEIGAFLRAAHCGRGMQQFEAQHHHSVGLVAHAVCGPKAVGLQWEVAVHACHAVTRLVAGLIDLGGDVPLEGLQIGLPEQPVPVIVVAADFGVQLVAVPGNHTAGEVVGQLVVVVGDVACLSRGNLPHFVSPDHEAVGVHVCEAQVVQLGRGHAVALECEEGGEVVQHGVVGHAIADPLPVPGVHRGESGGIEHLVEGAQIGDIGEPHDGFGGLHPEVAGLVDALFHGEGLQGALCLAQRIQSTIHGVGDGAVLVVLQQEGSRLQVAHIVSGGTSCPSAAAIARCQVASVQGQQCLKPGDVDADGQIHQGFQSREALRQIPAEVDRGVLAVDLEVAVDVLKHELAQVLEVALLAFQVHQERLGHVLEGAVVGAAVHPELAFHPALVVLVVVDVQEGVVAELELAHFDDHVGGVVHDQQALGLAVQCGAEDPASDDVGLLGAGKVHPVVEGQHGVVESLGAIGAGDGVEPGHVAEERQEQVLGRVQHAGSEHLVGVVHASGKAVGV
Then I pasted the ORF here and clicked "Run BLAST": https://www.uniprot.org/blast. McKernan ran his BLAST search in late 2023, but I ran the search several months later when there had been more sequences added to the UniProt database. So now the spidroin protein only came on third place, but the best two matches were a protein from algae and a cockroach protein. But all of them had a poor match with only about 25% identity:
From the table above you can also see that the match to the misannotated spidroin protein has a length of 1,496 aa and about 24% identity, but the matches to the next 5 closest proteins have similar percentage identities around 25% and length around 500-4000 aa. The match to the spidroin has an E-value of about 1.3e-9, which is meant to indicate how many similarly close matches are expected to occur by chance. But in this case the E-value is clearly too low, which might be because the query sequence had an unusual distribution of amino acids because it was the reverse complement of a codon-optimized sequence, but the E-value was calculated using the BLOSUM62 substitution matrix which assumed a natural distribution of amino acids.
ChatGPT said:
3. Query Composition Bias
- You mentioned the ORF comes from a reversed codon-optimized sequence.
- Codon optimization can create atypical amino acid distributions after translation, leading to stretches of sequence resembling glycine-rich or repetitive motifs.
- This can mimic spidroin-like sequences (which are glycine-rich) even though there is no functional homology.
- BLAST's substitution matrices (e.g., BLOSUM62) assume natural protein composition. With an unusual sequence, scoring becomes misleading.
4. Scoring Matrix and Gap Penalties
- Default BLAST parameters are designed for natural protein sequences.
- If the query sequence has biases (e.g., glycine-zippers, repetitive motifs), the scoring matrix may give artificially high scores for spurious alignments.
- This affects both the bit score and the derived E-value.
5. Statistical Assumptions Violation
- BLAST's E-value assumes random sequence alignments under certain statistical models.
- For sequences derived from reverse strands or synthetic constructs, these assumptions no longer hold.
- Hence, the computed E-value is numerically correct but biologically meaningless.
Both the misannotated spidroin protein and the reverse ORF do in fact have a high percentage of glycine:
# download MaSp1 sequence from UniProt, McKernan's Pfizer plasmid sequence, and coding sequences of SARS-CoV-2
curl 'https://rest.uniprot.org/unisave/G1Y380?format=fasta&versions=18'>spidroin.fa
curl 'https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi?db=nuccore&rettype=fasta&id=OR134577'>pfizerplasmid.fa
curl -s 'https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi?db=nucleotide&rettype=fasta_cds_aa&id=MN908947.3'>sars2.aa
# find longest ORF on reverse strand
r=$(seqkit seq -rp pfizerplasmid.fa|seqkit seq -s);for x in $r ${r:1} ${r:2};do sed 's/.../& /g'<<<$x|grep -Po 'ATG.*?(?=(TAA|TAG|TGA))'|tr -d \ ;done|awk '{print">"NR}1'|seqkit translate|seqkit sort -lr|seqkit head -n1 >reverseorf.fa
# make file where first column shows sequence name and second column shows amino acids
(seqkit seq -s sars2.aa|paste -sd \\0 -|sed 's/^/sars2 /';for x in spidroin reverseorf;do echo "$x `seqkit seq -s $x.fa`";done)>spidsilk
# make table of amino acid percentage in each sequence
awk '{split($2,z,"");for(i in z){a[z[i]][$1]++;sum[$1]++}}END{o="aa";for(j in sum)o=o" "j;print o;for(i in a){o=i;for(j in sum)o=o sprintf(" %.1f",a[i][j]/sum[j]*100);print o}}' spidsilk|sort -nk4|column -t
The output shows the percentage of each amino acid sorted by the column for the reverse ORF:
aa spidroin sars2 reverseorf Y 0.1 4.6 0.1 M 0.3 2.1 0.2 W 0.0 1.1 0.2 N 0.5 5.5 0.9 T 2.5 7.4 1.0 K 0.3 5.8 1.2 F 0.2 5.1 1.8 P 1.3 4.1 3.0 C 0.3 3.0 3.1 I 2.7 5.2 3.2 R 6.4 3.6 3.2 S 0.6 6.8 3.5 E 2.3 4.5 5.2 D 10.2 5.2 5.9 H 5.3 1.9 7.6 Q 10.1 3.8 8.0 L 2.7 9.5 11.7 A 22.4 6.8 12.3 G 18.0 5.9 13.6 V 13.9 8.0 14.2
ChatGPT said:
Spider silk proteins (spidroins) and the reverse open reading frame (ORF) of the Pfizer plasmid exhibit similar amino acid compositions, but for entirely different reasons. In the case of spider silk, the biased amino acid composition is a result of evolutionary selection for mechanical properties such as strength, elasticity, and hydrophobicity. Spidroins are rich in glycine and alanine, which contribute to flexible and crystalline regions of the silk, respectively. Leucine and valine are also prominent, helping to stabilize hydrophobic interactions. Conversely, spidroins contain very low amounts of aromatic residues (tryptophan, tyrosine, phenylalanine) and polar charged residues, as these are not advantageous for the physical properties of silk fibers.
In contrast, the reverse ORF from the Pfizer plasmid is not a biologically meaningful protein. Its amino acid composition is an artifact that arises from codon optimization used to express the vaccine gene efficiently in human cells. Codon optimization increases the frequency of certain nucleotides, particularly guanine and cytosine, to match human codon usage preferences. When this optimized sequence is taken in reverse and read in an alternative frame, it produces a pseudo-protein sequence with an amino acid composition that reflects these underlying nucleotide biases rather than any functional protein-coding information.
As a result, the reverse ORF also shows a high abundance of glycine, alanine, leucine, and valine. This is because codons rich in guanine and cytosine frequently map to these amino acids when read in the reverse complement strand. Other residues like glutamine, aspartic acid, and histidine also appear with elevated frequencies due to similar codon artifacts. The similarity in amino acid composition between the spidroin and the reverse ORF is therefore coincidental, stemming from the statistical properties of the genetic code and the influence of codon optimization, rather than from any evolutionary relationship.
This convergence in amino acid composition leads to misleading BLAST results. BLAST scoring is affected not only by exact sequence identity but also by overall composition similarities. Consequently, even sequences with low identity can produce low E-values if their amino acid distributions are comparable. In this case, the reverse ORF's accidental resemblance to spidroin composition results in false-positive BLAST hits, despite the lack of true homology. This reflects a composition-driven artifact, not an indication of biological relatedness.
The spidroin protein is no longer returned as a match by UniProt. The protein was deleted from UniProt in June 2024 for the reason that that it was an "excluded proteome": [https://www.uniprot.org/uniprotkb/G1Y380/history]
UniProt says that reasons for excluding a proteome include incorrect assembly, contamination, or misidentification of the source organism. [https://www.uniprot.org/help/proteome_exclusion_reasons]
The source organism of the protein at both UniProt and GenBank listed is a bacterium called Nitrospirillum amazonense. But bacteria do not produce spider silk unless they have been modified genetically, and the protein sequence came from a paper which described a natural species of bacteria and not genetically modified bacteria.
The entry for the protein at UniProt was copied from this entry at GenBank: https://www.ncbi.nlm.nih.gov/protein/EGY00023. The entry at GenBank includes some metadata that was missing from UniProt, including a note for the CDS that says "identified by sequence similarity; putative".
ChatGPT said:
The entry shown for Nitrospirillum viridazoti Y2 listing "Major ampullate spidroin 1 MaSp1" is likely a case of misannotation due to automated sequence similarity searches. Here is why this happens:
Annotation by Homology: The GenBank entry notes that this sequence was "identified by sequence similarity; putative." This means that during the annotation pipeline, the protein sequence showed local similarity to known spidroin sequences, possibly because of repetitive glycine- and alanine-rich regions or structural motifs that resemble spidroin proteins. Such repetitive domains are common in unrelated proteins across various species.
Spurious Similarity to ATPase Domains: The region annotation (COG3903) refers to a predicted ATPase domain, which is a general function category not specific to silk proteins. ATPase domains are found in many proteins across life forms. The resemblance to spidroins might arise from structural repeats or motifs that coincidentally align with spider silk sequences, especially in large, repetitive bacterial proteins.
Conceptual Translation Artifact: The comment mentions "Method: conceptual translation," indicating this is a predicted open reading frame (ORF) from genome sequencing data, not experimentally validated. Large bacterial genomes often contain long ORFs with repetitive low-complexity regions that can artifactually match spidroin sequences in databases.
Misleading Product Naming: The product is named "Major ampullate spidroin 1 MaSp1," but this is a bioinformatic label assigned due to sequence similarity, not functional evidence. No experimental data supports that Nitrospirillum viridazoti produces spider silk proteins.
Source Confusion: Nitrospirillum viridazoti is a nitrogen-fixing bacterium associated with plants, not arachnids. There is no biological reason for it to produce silk proteins. The naming likely results from a bioinformatics pipeline matching a segment of bacterial protein to a spidroin database entry.
This lady on Twitter said that the spidroin clots can be activated remotely (which is similar to the theory by Mike Adams that the calamari clots contain electric circuits that can be triggered by 5G to kill people): [https://x.com/LouiseBrookes8/status/1904546516292821189]
Someone on Twitter said that the reason why the clots are stained by Thioflavin T might be because spidroin has amyloid-like properties: [https://x.com/mvwinds/status/1863467028960706983]
Ulrike Kämmerer said that the reverse ORF actually codes for spider silk, but she didn't mention anything about how the ORF only had an extremely distant match to a spidroin sequence at UniProt, or how the sequence was misannotated. And she said the spidroin is extremely durable, and that once the human body has been instructed to form spidroin, the spidroin can no longer be degraded because it is a foreign protein, which will lead to the buildup of spider silk inside the body. She said it was similar to the accumulation of prions in mad cow disease, and she said the spider silk will destroy cells as it accumulates in human tissue. And she said that Arne Burkhardt had found symptoms of a new type of amyloidosis in people who died from a COVID vaccine, which she speculated might have been due to the spidroin protein. [https://www.aussie17.com/p/biologist-prof-dr-ulrike-kammerer]
Ana Maria Mihalcea has a unique theory on how the calamari clots are formed, because she told Mary Holland from CHD that the clots are formed when nanobots eat red blood cells: "I analyzed these clots microscopically and found these nanotechnological filaments in there. And Clifford Carnicom and I - we also did chemical analysis on them. I also filmed how the clots actually assemble. What you see is unvaccinated blood, the nano robotic swarm. You see all these green and orange and yellow lights. And they are hijacking the electricity from the red blood cells, and they're killing them basically to feed themselves. It's called energy harvesting, it's well described in the nanotechnological literature. And so these robots then, what they leave in their wake is this. This is the same blood 30 minutes later. The blood is completely destroyed. The robots have moved on. And this is the rubbery clot that we've been seeing. And that you can see how it self-assembles, and literally builds when you are leaving the - when you're drawing the blood, and you are leaving it out for at least four hours." [https://rumble.com/v5gadat-what-is-in-our-blood.html?start=2510] The image below shows her "nanorobotic swarm" of green and orange and yellow lights (and it's also depressing to note that her interview with CHD has 101 upvotes and 1 downvote on Rumble):
During the interview with Mary Holland from CHD, Mihalcea also said:
But somehow Mary Holland didn't have anything critical to say to Mihalcea, and she never asked Mihalcea questions like "How do you know that?" or "What's your source?" or "How can you see nanotechnology with a light microscope?" or "Isn't that just Brownian motion and not quantum dots?"
Ana Maria Mihalcea wrote that Hirschman's clots contained Morgellons bacteria and Morgellons fibers: [http://web.archive.org/web/20230711070359/https://anamihalceamdphd.substack.com/p/blood-clot-analysis-from-living-and]
Our findings:
- The filament structure is a 1:1 match to our previous findings as well as consistent with 30 years of research done by Clifford Carnicom.
- Cross Domain Bacteria, the origin of filament genesis are visible within the clots
- This appears to produce an amorphous protein structure
- Stray blood cells are present
It appears that the rubbery clots are a more advanced and extreme evolution of the CDB/ Morgellons filaments.
CDB or cross-domain bacteria is Clifford Carnicom's name for the supposed causative agent of Morgellons disease. Ana Maria Mihalcea also claims that chemtrails contain both Morgellons fibers and spider silk: [https://www.google.com/search?q=site:anamihalceamdphd.substack.com+chemtrail+spider+silk]
In September 2023 Richard Hirschman wrote this about his clots: "I know that there have been some people looking into them. publicly the only people who have spoken about what they have found or seen are, Dr. Ryan Cole, Dr. Ana Mihalcea and Mike Adams. There have been others but I am not aware of any of their findings." [https://x.com/r_hirschman/status/1700596168256880863] But if Hirschman was for real, would he have wanted Ana Maria Mihalcea to say that his clots contained Morgellons fibers, Morgellons bacteria, and spider silk? Or would he have wanted Mike Adams to say that his clots contain electric circuits and nanowire interface structures? I haven't found him denouncing the claims by Mike Adams or Ana Maria Mihalcea anywhere. [https://x.com/search?q=from%3Ar_hirschman+%28mike+adams+OR+mihalcea%29&f=live]
Ana Maria Mihalcea is a member of a neo-Theosophical cult called Ramtha's School of Enlightenment. Their leader JZ Knight claims to be channeling a 35,000-year-old Lemurian ascended master called Ramtha. Mihalcea wrote a document about the medical miracles that were manifested in the body of JZ Knight, which included that JZ Knight's DNA changed to male DNA while she channeled the ascended master: [https://docs.wixstatic.com/ugd/72ba1c_2971020dc9154de89ba121994d187882.pdf]
An account that promotes Miles Guo posted this video where Ana Maria Mihalcea said that she had found spider silk in calamari clots. The video included this slide about the reverse ORF from a presentation by David Speicher, which featured a photo of calamari clots as if the clots were somehow related to the reverse ORF: [https://x.com/aus_mini/status/1813411573085692059]
In an interview David Speicher did in September 2024, he said: "If you encode going reverse, you get another intact open reading frame that's perfectly intact. You get this whole fibroin heavy chain, which is major ampullate spidroin 1, MaSp1. And that is the same fibroin that's found in silkworm silk. And what are we pulling out of the dead vaxxed people? All of these white fibrinous clots. And these silk proteins are used in spider silk. The thing about spider silk is that if it's in the spider at the right pH and the temperature, it's a liquid form. If it's outside and it cools and the pH changes is when things start to solidify and make silk. So I think - and a lot of groups worldwide are looking at this - but there could be a major link between these clots and what's actually in the intact plasmid DNA." [https://www.drtrozzi.news/p/genetic-invasion-an-update-with-dr, time 27:28]
Speicher showed the slide below where the percentage identities of the matches were covered up, so people couldn't see that the matches had only about 25% identity. His amino acid alignment still showed that most positions of the alignment did not match, but many members of his audience probably did not understand what the alignment meant. And Speicher didn't say anything about how the match to the spidroin protein had an extremely low identity and how it was likely due to chance:
When Speicher said that "you get this whole fibroin heavy chain, which is major ampullate spidroin 1, MaSp1", he mixed up the spider silk protein that was the first match with the silkworm silk protein that was the third match. But they were two different proteins, and the fibroin was not a spidroin or vice versa. However both proteins had the host species listed as a species of bacteria which doesn't produce either spider silk or silkworm silk, so both sequences were likely mislabeled, and they have both now been deleted from UniProt.
Speicher also showed this slide which suggested that the calamari clots might be connected to the reverse ORF:
Speicher has a PhD degree in virology, and he has a postdoctoral fellowship in bioinformatics, so I have a hard time believing he would be stupid enough to think that the reverse ORF would actually code for spider silk. It seems more likely that he is deliberately promoting disinformation. But he is also one of the main people who has pushed Kevin McKernan's narrative about DNA contamination, which I think increases the likelihood that it's a disinformation narrative (even though the DNA contamination itself seems to be real, but its implications seem to be vastly exaggerated by McKernan and Speicher). But it's interesting that McKernan is now also one of the people who is supposed to have analyzed the calamari clots in a lab.
In October 2023 a preprint about DNA contamination was published by David Speicher, Jessica Rose, Maria Gutschi, David Wiseman, and Kevin McKernan. [https://osf.io/mjc97_v1/] In 2023 Maria Gutschi did a presentation where she said: "So Kevin and group tried to determine what does this protein make - what does mRNA make. The closet thing they found was silk protein, spider protein. Spider silk. Wow. And so, we don't know if that's happening or not - there's a lot that needs to be done - and whether that is the case. But it is a large concern on my side. Because it is not an accident that this mRNA is there on the opposite side. In my opinion it's not." [https://crowdbunker.com/v/23fVajqu, time 26:25]
Jessica Rose has written many Substack posts where she has presented Kevin McKernan's findings in a popularized format. She also wrote a Substack post about the reverse ORF, where she wrote about spidroins as if they would somehow be relevant to the reverse ORF, and as if people needed to learn about spidroins to understand the reverse ORF. [https://jessicar.substack.com/p/what-a-tangled-web-we-may-have-weaved] But she didn't say that the reverse ORF just matched the spidroin protein by chance, and the spidroin had nothing to do with the reverse ORF, and there were many other random proteins which had a similarly close match. And she didn't even post instructions on how people can repeat the BLAST search themselves or how people should interpret the BLAST search. I called her out for how misleading the post was, because she must have known it would be misinterpreted by her readers. [https://x.com/henjin256/status/1848961827415249112] But Jessica Rose also has a PhD degree in the computational biology of viruses, so her post seemed like she was deliberately trying to mislead people.
In March 2025 Richard Fleming published a PDF by the Czech biologist Soňa Peková, who is supposed to have verified McKernan's finding of DNA contamination, and who is basically the Jessica Rose type figure of the Czech Republic. It might be a coincidence, but Soňa Peková is a member of a neo-Theosophical cult called ALLATRA that has many similarities to Ana Maria Mihalcea's cult: https://jessicar.substack.com/p/the-new-slovakian-report-showing/comment/100916301. ALLATRA teach that reality is oppressed by Draco Reptilians, that Slavs are the oldest ethnic group after the fall of Atlantis, and that there is a 12,000-year pole shift cycle. In one of her interviews Soňa Peková talked about Pleiadian aliens and 5D ascension, and she said that Gaia has the capability to reach not only 5D but 9D reality. Even though the cult is overtly based in Ukraine, they run a multilingual media operation that produces content in various languages, and their most popular content are English-language deep fake videos that employ the avatar of the American veteran spook Egon Cholatkian. In the same way that Scientology is partnered with the Nation of Islam, ALLATRA is also partnered with an African American freemasonic lodge called the World's Masonic United Nations.
A user on Twitter said that the clots in the thumbnail of this video were "calamari-like clotting", even though the clots were inside a surgery drain tube: [https://x.com/CheweyLife/status/1914528829890068632]
But an MD user replied: "Uhm, yeah. After week of surgery drainage, white clotting in them is not unusual at all. After all its the fibrin rich wound secretions drained through plastic tubes. Usually you pull them, before they clot. Its totally different to havin white clots build-up inside blood vessels". [https://x.com/53v3n0fn1n3/status/1914690994529849616] The user also wrote: "Clotting cascades are triggered on the wounds surface. Clotting in these tubes starts when the suction doesn't work properly. Some get them, some don't. Lymphadenectomy can leave a huge wound inside, so drain is left as long as secretion keeps going, weighed with inf. risk."
Later when another user posted a video of the clots in a surgery drain tube, the MD user pointed out that it was a surgery drain tube, and that wound secretions that are drained by the tube have a high fibrin content: [https://x.com/53v3n0fn1n3/status/1915703836171215355]
Richard Hirschman also shared the same video by the lady who showed the clots in a surgery drain tube, and he wrote: "The clots she shows look very similar to the ones that I have been seeing during the embalming process, the difference is she's alive and those who I embalm are not. If the clots are the same, they can't just be postmortem. There was a vascular surgeon whistleblower who spoke with Dr Philip McMillan about the same type of clots that he has been seeing. How does a vascular surgeon remove postmortem clots during the surgery on a living person?" [https://x.com/r_hirschman/status/1914458661021475307]
In March 2024 NZDSOS tweeted this photo of "rubbery white structures being discharged through a surgical wound drain site" (but it may have just showed regular clots in a surgical drain tube): [https://x.com/nzdsos/status/1767386236925387026]
The earliest place where I found the same photo posted was in the blog of NZDSOS, where the photo was not given any source but its caption said "Photo Provided for Use - Copyright Free". [https://nzdsos.com/2024/02/20/rubbery-clots-campbell/] So I guess it's an original photo published by NZDSOS.
Greg Harrison also posted the photo and two other photos which he said were clots that came from living subjects: [https://x.com/Greg21143362/status/1776172411819594066]
Some of the clots that are presented as calamari clots may have been created by a device like a Chandler loop device, where blood is repeatedly passed through a tube until clots form in the tube. Here's images of blood clots created with a Chandler loop device (where the scale bar is 2 cm, so the longest clot in image L20 is about 30 cm): [https://link.springer.com/article/10.1007/s10856-023-06721-7]
The image below demonstrates how the device works: "A photo of the assembled Chandler loop apparatus with blood running in the device. C Illustration depicting clot formation within the Chandler loop at the forward meniscus".
In another study a Chandler loop device was used to produce clots that had close to a pure white color, as can be seen from images A and B below: [https://link.springer.com/article/10.1007/s10856-024-06775-1]
In order to manufacture clots with the amyloid properties observed by Kevin McCairn, perhaps bacterial LPS could be added to the blood to induce misfolding of fibrin, like what was done by Pretorius and Kell who wrote: "Here, we show that the addition of tiny concentrations (0.2 ng l(-1)) of bacterial LPS to both whole blood and platelet-poor plasma of normal, healthy donors leads to marked changes in the nature of the fibrin fibres so formed, as observed by ultrastructural and fluorescence microscopy (the latter implying that the fibrin is actually in an amyloid β-sheet-rich form that on stoichiometric grounds must occur autocatalytically)." [https://pmc.ncbi.nlm.nih.gov/articles/PMC5046953/]
Laura Jeffrey said that the new type of white clots often had red clots attached to their end, so that the white clots appeared to be feeding on the red clots. A similar story was told by Hirschman, the anonymous embalmer whose photos were shown by Jane Ruby, and the Canadian funeral director Carolyn who was interviewed by Epoch Times.
But normally red clots form in veins and white clots form in arteries, so it would be unusual to see both type of clots in the same blood vessel type. ChatGPT said:
- Venous thrombi (often called "red thrombi") form under low-flow conditions and are composed mainly of fibrin and red blood cells, giving them a darker appearance. However, they also contain platelets.
- Arterial thrombi (often called "white thrombi") typically form under high shear stress conditions and are composed predominantly of platelets and fibrin. These clots are more compact and pale due to the relative scarcity of red blood cells.
"Currant jelly clots" are postmortem clots, but they also form in veins and not arteries. Normally both in the case of post-mortem clots and clots that are seen in living people, the red clots are more common in veins but white clots are more common in arteries. ChatGPT said:
Currant jelly clots are a type of postmortem clot that typically form in veins and the right side of the heart due to the low-pressure, slow-flow conditions present in these areas after death. They appear dark red, soft, gelatinous, and homogeneous, resembling currant jelly, which results from the settling of red blood cells and fibrin in the absence of circulation. These clots are not adherent to the vessel wall and can be easily removed, distinguishing them from antemortem thrombi.
In contrast, arteries operate under high pressure and fast flow, both in life and during the early postmortem period. These conditions make the formation of currant jelly clots in arteries unlikely. Instead, after death, arteries may remain empty, or they may contain pale "chicken fat" clots, formed from the separation of plasma and red cells. The rapid flow in arteries prior to death and the lack of blood stasis afterward do not support the layering and sedimentation needed to produce the appearance of a currant jelly clot.
Because of these differences in hemodynamic conditions and postmortem physiology, currant jelly clots are not found in arteries. Their formation is a product of the low-flow, static environment of the venous system and is considered a normal postmortem finding rather than a pathological process.
Regular white arterial clots don't normally reach a length longer than a few cm. So if long calamari clots would form in the arteries of living people, it would make them distinct from regular white arterial clots. ChatGPT said:
White arterial thrombi, also known as white clots, are typically relatively short in length compared to venous thrombi. They commonly measure from a few millimeters to a few centimeters. In rare cases, particularly in larger arteries such as the aorta or carotid, they may extend to several centimeters. However, such instances are uncommon.
These thrombi form under conditions of high shear stress, where rapid blood flow and endothelial injury - often due to atherosclerotic plaque rupture - promote platelet activation and fibrin deposition. The resulting thrombi are firm, pale, and platelet- and fibrin-rich. They are usually attached to the vessel wall at the site of injury and do not extend far longitudinally, as the high-pressure arterial environment tends to fragment or dislodge longer thrombus formations.
In contrast, venous thrombi can grow to lengths of 20-30 cm or more, often forming extensive casts of the affected vein. This is due to the lower flow conditions in the venous system, which allow more gradual accumulation of fibrin and red blood cells.
For example, in myocardial infarction, the thrombus that occludes a coronary artery is typically only a few millimeters long, yet sufficient to block blood flow. In summary, white arterial thrombi are usually short, often less than 5 cm, with longer formations being rare and limited to larger arteries.
Philip McMillan offers a free online course about the calamari clots, which is basically just a website where you have to enter an email address in order to see the content. The course features a section titled "Observations from Endovascular Surgeon", which consists of a 5-page document that looks like a letter from a surgeon to McMillan: [https://vejonhealth.learnworlds.com/course/embalmers-clots-composition-and-cause, f/mcmillan_letter_from_endovascular_surgeon.txt]
The surgeon wrote that they had not seen calamari clots in their lab: "Anyway, I was looking for examples of what I heard your guy talking about. We also did a lot of vein patients but, once again, though I was watching out for these cases, I never saw/heard about any of our patients (and we had a very active Vein Practice, at least prior to Covid) having extensive venous blockages like your witness produced. DVT's are not that uncommon in a very busy vein ablation practice. We were doing upwards of 30-45 venous ablations a week, on average, prior to Covid. Covid really did a number on us, like other clinics, especially when people started locking down. But the DVT's that we experienced post mRNA Vaccine deployment, and once again, the vast majority of our patients were mRNA vaccinated, their clots were easily managed and fully resolved with a course of anticoagulative treatment, usually within 2-3 weeks. There had to be one in there, but maybe we just didn't identify it."
The surgeon also wrote: "Without understanding the timing of onset of theses white, fibrous clots, when they began forming, either weeks/months prior to their event or just days before their event, I don't know how we could have missed these blockages during the procedures. Moreover, all of our patients, within a week or two prior to a venous ablation or arterial intervention, had a full vascular ultrasound study that would certainly have demonstrated these obvious tissue amalgamations, even the smaller ones. Most certainly the larger ones I've witnessed on your podcasts with your whistleblowers and your embalmers. No way, with our technologist talents, could these growths have been missed."
The surgeon speculated that the reason they weren't seeing the clots may have been if the clots formed soon before death: "The only real conclusions I can come to, during the entire time of witnessing our practice's patient demographics and the procedures we performed on them, and many of them were repeat customers, sometimes requiring multiple repeat annual interventions, is that these blood clots, fibrous or jelly, must happen rather abruptly, because our patients typically receive follow up vascular Ultrasonography 2-3 times per year, and we never noticed these large blockages that would certainly, without a doubt be able to visualized. Our equipment was the best. Our very best techs would have found them too. My surgeon partner looked at every single study personally. Nothing out of the ordinary, anyway. So this makes me hypothesize that these structures must form very quickly in an acute way, resulting in the patient needing an emergency trip to the hospital, or dying and going to the embalmers." However for example Tom Haviland has said that the reason why morticians say they only started seeing the clots in mid-2021 might be if the clots take about half a year to form. And Nicky Rupright King said she didn't start seeing the clots until 2022, and she suggested the clots might take more than a year to reach their full size. And anyway if the clots only take days to form, then why weren't embalmers already seeing the clots in January 2021?
The surgeon who sent the letter to McMillan wrote: "Unlike the clinic of the Whistleblower in your podcast, that was a hospital that did every body part, from the brain to the heart to the lower extremities, we were limited to doing pelvic and lower extremity endovascular atherectomies and angioplasties. Of course we did some stenting, when necessary." But I don't think that would explain why people in his lab were not seeing any calamari clots. A more likely explanation is that the clots are a hoax, and McMillan's cath lab whistleblower was lying.
I didn't find the surgeon's letter published anywhere else. I also haven't heard McMillan mention the letter anywhere, and I didn't find it published on his blog, which might be because the letter conflicts with the narrative about the clots he is trying to present to his audience.
In May 2023 Stew Peters released a sequel to the Watch the Water film, where Bryan Ardis said that COVID was caused by snake venom in tap water. [https://rumble.com/v2nh8xc-premiere-watch-the-water-2-closing-chapter.html]
At time 14:48 Ardis said: "The actual textilinin protein from the eastern brown snake prevents your body's plasmin from breaking down the blood clots. And it's published by them. We have created a self-assembling nanoparticle hydrogel that causes rapid blood clotting, rapid blood clotting. And it is resistant to plasmin being able to break it down, warfarin from being able to break it down - which is cuminin, a blood thinner - and it's also heparin resistant. And what did you find in every ICU with COVID-19 patients? They were heparin resistant. Why? They had ecarin in their body and textilinin." Then Stew Peters asked: "Is that what's causing these white fibrous things that embalmers are finding?" And Ardis replied: "1000% that's what's causing them." So Ardis said he was 1000% sure that the calamari clots were caused by two snake venom proteins.
At time 37:46 Stew Peters pointed out how Ardis was holding a vial with calamari clots when he spoke on the ReAwaken America Tour. And Ardis said they were clots he got from Richard Hirschman, and he again said that the clots are produced by a hydrogel that contains snake venom proteins. And he also talked about an Italian paper by Carlo Brogna et al. where the authors found snake venom peptides in the blood and urine of COVID patients.
At time 40:41, Ardis said: "Just January 28th of 2023, just a few weeks ago, Dr. Chetty MD out of South Africa - is working this entire time. I have been on Zoom calls with this guy for three years now, as we're learning about COVID, how to treat COVID, the success they're seeing in South Africa. Dr. Chetty is a great, honest, ethical human being. He has done phenomenal work. He stated in an interview on January 28th, 2023 - that in long-hauler COVID patients who are coming to his clinic from around the world - they couldn't get them better with traditional therapies they found worked with other COVID patients. So they ran fecal tests on them to find out is there anything in their body we're unaware of that would keep these people sick with long-hauler COVID symptoms?" Then the video cut to a clip where Shankara Chetty said: "At that point that we realized we need to look at stool samples. We need to - if it was found in sewage, and I couldn't understand why a virus found in sewage was not tracked backwards to the gastrointestinal tract weight arose, and to figure out what it was doing there. And so we managed to contact Carlo Brogna, who's done some very interesting work on coronavirus. What he very basically discovered with looking at stool samples was that the virus was replicating somehow in these stool samples, and the stools had toxins - protein-based toxins in them. He found with the incubation of the supernatant of this sample on fresh uninfected stool that the viral title rose exponentially and so the toxins as well. And so he proved bacterial phage activity, that this virus has the ability to infect the bacteria of your gut. And he found toxicities there, toxin-like peptides, which were akin to many different kinds of snake venoms, sea-snail poinsons, shellfish poisons, and it's a wonder how those got there." Then Ardis said that venoms are manufactured synthetically both using bacteria like E. coli and using mammalian cells, so the mRNA vaccines also contain instructions that cause both bacteria and human cells to produce snake venom.
Shankara Chetty wrote that long COVID was caused by bacteria producing snake venom, and that he first looked into snake venom because Tau Braun told him to keep an eye on snake venom: [https://x.com/ShankaraChetty/status/1900893736399217058]
Tau first mentioned snake venom to me in 2021 to keep my eye on. He understood that it was being experimented on to be weaponised and could be aerosolized etc.and spread, but I couldn't figure the transmission to other individuals by those affected. He planted the seed and asked that I don't disregard an envenomation as my treatment would address both Envenomation and Hypersensitivity. With the chronic gut issues we were seeing and a positive rectal PCR swab reported early on from China, we contacted Carlo Brogna, who was examining stool. What he found was that the virus had bacteriophage activity and infected the bacteria in your gut, replicating in them and getting them, through insertional mutagenesis, to produce toxins. These toxin like peptides resemble many different kinds of snake venom, conotoxins (sea snail venom), and starfish toxin.
That was the revelation that solved all my questions. Transmission of the toxin occurred through transmission of its code by the virus to the gut bacteria that then made the toxin. This allowed the toxic proteins to evade the hosts' digestive enzymes in the stomach and small intestine by being made directly in the colon where it can be absorbed unaltered.
UNNATURAL, INTENTIONAL, WELL PLANNED, TRANSMISSIBLE ENVENOMATION.
Chetty also tweeted: "Tau is one of my guardian angels, and an ex South African to boot." [https://x.com/ShankaraChetty/status/1900576881906200893]
Tau Braun's bio says that he is a "U.S. National Counterterrorism & EMS Advisor and Trainer" and that he has been a speaker at a bunch of emergency management conferences. [https://www.drtaubraun.com/about] In 2022 he told Jane Ruby that calamari clots are tissue that was programmed to grow snake venom glands by nanobots that used graphene oxide as a delivery mechanism. [http://web.archive.org/web/20221115233622/https://stewpeters.com/video/2022/11/the-jabbed-are-growing-animal-venom-glands-and-ducts/]
Shankara Chetty is Philip McMillan's sidekick who is frequently featured in videos on the Vejon Health channel. Chetty was even featured in the video where McMillan interviewed the cath lab whistleblower who said that he saw calamari clots in living people:
I started to think that McMillan was likely controlled opposition after he published several videos and posts where he promoted Greg Harrison's ORF hoax, but McMillan's connection to Shankara Chetty gives me even more reason to suspect that McMillan is not sincere.