APM

Abnormal Polymer Mass - aka 'Calamari Clots'

This post will be an investigation into what I term Abnormal Polymer Mass - more commonly known as the calamari clots, or white rubbery structures associated with embalmers and the vascular system; often associated with ‘sudden death’ syndrome.

I do not like to use the term ‘clot’ for these structures; as we will see, they really do not resemble blood clots.

As unbelievable as it may seem, they are in fact a sort of living material, comprised primarily of synthetic biology (CDB) and associated proteins/metabolic products (I have also seen the term “Engineered Living Material” used to describe the APM).

Many may know that these are associated with dead people and embalmers, and are probably familiar with dramatic images like this one:

‘Calamari clot’ image.

I suspect far fewer are aware that this same material can be extracted via venipuncture and centrifugation from living individuals, seemingly irrespective of ‘vaccination’ status:

APM immediately after centrifugation process, visible on top of blood pack.

APM with blood still attached.

I have been removing and examining these masses for many months. I have settled upon a method of extraction that I wish to share with anyone interested.

I will note here that this method is very likely modifiable, has only been used on myself (I have extracted this material many times using different methods), and is not based on any specific nor rigorous scientific backing. It works, demonstrably and repeatedly, and is an excellent way to retrieve this material as needed for experimenting and examination.

I also wish to give credit to Ronald Norris, who did significant work on the extraction process and forms the basis of what I present in this article.

We will then look at the APM under the microscope, and I will note some further unusual properties.

Extraction Methodology

The process involves drawing of blood via venipuncture into a vacutainer tube, immediately centrifuging it, allowing it to sit, and then centrifuging again at a higher rpm.

Venipuncture
A 6mL red top vacutainer tube is used. It has a minor clot activator in it. This is the only type of tube I have ever used and I am unsure if there are differences in APM retrieval with different types; I suspect there is.

Approximately 6mL of venous blood drawn into vacutainer tube.

First Centrifuge (1600 for 15 minutes)

The blood is immediately (not allowed time to coagulate) centrifuged at 1600rpm for 15 minutes.

As far as I understand, this technique (draw and immediate centrifuge) is used in the medical field to extract platelet rich fibrin (PRF). This material is the cloudy looking area above the blood clot (somewhat difficult to see in these pictures; two vials shown). I believe PRF is a normally occurring hydrogel that is produced by the body. The nature of the APM is distinctly different from PRF.

Vials after 15min@1600rpm - cloudy area above packed blood; this consists largely of PRF, which could be considered normal.

At this stage, the APM can possibly be partially seen directly above the packed blood.

Rest Period (15 minutes undisturbed)
The vial is then allowed to sit undisturbed for another 15 minutes.

After the initial spin, the vial is allowed to sit undisturbed for 15 minutes.

Second Centrifuge (2200rpm for 15 minutes)
After 15 minutes has elapsed, the vials are then centrifuged again at 2200rpm for 15 minutes.

Second centrifugation; 2200rpm for 15 minutes.

The final result will be the following:

APM isolated after second centrifugation.

Isolated APM with most of blood removed in petri dish.

I have performed some basic dissolution/solubility experiments on this material, which I hope to share in a future post.

For now, we will focus on microscopy of the APM.

Microscopy

An APM was extracted and had visible blood mechanically removed, then repeatedly washed in alternating distilled water and 99% isopropanol. A final washing in water, and then a small slice was dissected off the primary mass.
Slide prepared as in following image:

APM slice near center of slide, in red circle.

Micrographs are as follows. Objectives used are 4x/10x/20x/40x/100x. All images in brightfield.

Note highly filamentous nature. Individual comments will be under each image.

4x, general overview. Note very obvious filamentous nature, and protrusions around border. Clearly non-uniform texture and makeup, even at low magnification. Complexity evident.

Two additional micrographs at low magnification.

We now increase magnification.

10x objective; filamentous nature is even more apparent here.

An additional image at 10x objective; note larger filament in bottom right. These larger filamentous structures are often seen in the synthetic tissue scaffolding in general, often taking the form of large sheets.

20x objective; note layering of filaments and dense area to lower left.

20x objective; small round objects can be occasionally seen throughout (suspected CDB forms). Note filamentous protrusions on right; this will be examined more closely.

Filamentous protrusion on edge of APM. Individual CDBs can be seen within filament. Complete match to CDB morphology in CI research archives.

Higher magnification, complex filamentous nature dominates. Small round objects can be seen, and more unusual organized formations also become visible:

40x objective; highlighted in red is ‘chain link’ morphology, an unusual suspected form of CDB I have seen rarely.

Another image highlighting ‘chain link’ morphology.

100x objective, no oil used, individual CDBs come into view, match to historical CI research related to ‘Morgellons’ present within human blood.

100x objective, suspected individual CDB forms can be seen.

100x objective, individual CDBs visible. Complex sub structure evident. Again, match to CDB forms in CI research archives.

Electrolytic Protein(?) Production
During investigation into the nature of the APM, I have discovered a rather unusual and striking property (although not a surprising one, if they are indeed synthetic biology): the ability of the APM to produce large quantities of an apparent red-brown proteinaceous material while under electrolysis:

Image showing APM (red circle) and large quantity of reddish-brown proteinaceous material (green) formed over time while under electrolysis. The APM is also covered in this material.

Another image showing floating APM and large quantity of proteinaceous material.

This material is very similar visually and microscopically to large portions of the residue produced during electrolysis of whole blood (see article Transformation for details). It does not appear to be parts of the APM ‘converting’; it is being produced through some other mechanism.

The material and phenomenon itself is worthy of much investigation; for now, it is worth mentioning that it simply exists.

I suspect it is a protein produced by the CDB, the production of which is stimulated by electrical energy. The quantity the APM can produce is very impressive, again similar in nature to the transformation of whole blood.

There is substantial historical CI research into a reddish-brown proteinaceous material, precisely resembling what is seen here.

The CDB appears to be highly efficient in absorbing and utilizing energy. CI research has a long history of documenting strong electromagnetic (and other forms of energy) relationships with the CDB.

To finish the article, I will provide relevant CI articles on this subject; these are merely culminations of decades of work.

I reiterate here, and will continue to do so: all relevant research can be found in the CI research archives, at carnicominstitute.org.

https://carnicominstitute.org/maturation-of-a-biopolymer/
https://carnicominstitute.org/pandoras-polymer-synthetic-blood-and-the-cross-domain-bacteria-cdb/
https://carnicominstitute.org/a-cross-domain-bacteria-cdb-production-otherwise-known-as-hydrogel/

https://carnicominstitute.org/human-blood-vs-synthetic-blood-the-path-to-the-blood-clot/

https://carnicominstitute.org/the-polymerization-clotting-of-blood-a-model/

I hope to expand my thoughts on the APM in a later post, and provide more analysis of the material.

Thank you for taking the time to read!

Michael Merrick