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I believe there's 2 types of cold forming hydrogel we're dealing with. The Sodium Citrate deals with the calcium polymer. Thanks Karl C and Clifford. 👍☺️

The other cold formed soft white hydrogel, uses many Nano heavy metals as cross linkages, hence

the uniformity in its assembly. It also has a tunability, via photoswitchability.

The reason the polymers have acidic tendencies, the technology also uses a H+, proton pump.

The Amyloid fibrils are also part of the self assembly, it what makes the polymer hydrogels. Its process is similar to that of a Prion disease. The Amyloid elongate, become more polymer like and attach to the Nano heavy metals to form a cross linked mesh.

I'm going to write post soon. I got more literature to read, I think we'll have a protocol for disassembly and prevention.

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Interesting, unfortunately as of yet when I test the congo red dyed structures they do not show up as amyloid when viewing with polarized light microscopy. They should go from red to yellowy green. but so far no go. I will continue to replicate this test occasionally. Soon we should know how many hydrogel products are in there and what they are based on. I have more dyes coming today and soon we will use other techniques too. Thanks for reading and supporting !

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Does the Congo red dye attach to the hydrogel and remain red, or does it not attach at all?

I'll keep the dyes in mind, as I remember some experiments in the literature use dyes.

I take a guess the red dye doesn't attach at all.

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Congo red mainly attaches to material loaded inside the hydrogel matrix, not the hydrogel itself. I have alcian blue arrived today for dying alginate hydrogels which I will be using in conjuction with the fast green again for chitin based hydrogel.

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That's very interesting, can't wait to see the alginate hydrogel died blue.

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Karl, You may want to check this medical science abstract-Health Effects of Exposure to Ultrasound and

Infrasound-pgs34-36. The bubbles may be inertia cavitation bubbles. If you check my blood, you will see thousands of micro air vapor bubbles. I am being tortured daily with sonic lasers causing acoustic cavitation of soft tissues especially abdomen where a lot of air and intestinal gas is accumulated causing stretching and enlargement of abdomen and internal organs and pain and suffering. When bubbles explode and collapse and during inertia cavitation they release mechanical pressure, heat, free radicals causing inflammatory, oxidative, hypertensive stress. Similar cavitation process occurs in boat propellers.

"2.3.3 Cavitation and gas-body effects

Acoustic cavitation may cause cellular responses as a result of mechanical, chemical or thermal means.

The inhomogeneous periodic field around a pulsating bubble can generate a small steady flow of fluid by a process known as microstreaming (Nyborg, 1998). The variation of this flow with distance from the bubble creates extremely high shear stresses near the bubble surface. It is now accepted that these

stresses are responsible for the observed temporary alteration in permeability (sonoporesis) and cell

membrane destruction resulting from exposure of cells in suspension in the presence of microbubbles. In

addition, mixing from microstreaming is the most likely explanation for enhanced drug transport through

the skin mediated by ultrasound. A bubble within a capillary bloodstream will stress that capillary when

forced to expand and contract in an ultrasonic field. These stresses may be sufficient to rupture the

capillary, allowing extravasation of the contents. Bubble collapse during inertial cavitation can also give

rise to a radiated acoustic shock wave into the surrounding medium. Inertial cavitation carries an

additional hazard for cells, free radical production. These highly reactive chemical species can be created

in the gas contents of an adiabatically collapsing bubble, because of the extremely high temperatures

and pressures created by the rapid bubble collapse. They may then be released to the surrounding

medium once the bubble fragments. However, in contrast to the association for ionising radiation

between free radical production and cell damage, free radicals produced by inertial cavitation lie outside,

rather than within, the cell. Whilst such free radicals may in principle migrate through the membrane and

damage intracellular components, both the presence of natural free radical scavengers and the very

short lifetimes mitigate against this. Were an intracellular bubble to undergo inertial cavitation, cell death

would be immediate. Finally, the presence of clouds of bubbles increases the absorption coefficient of ......"

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this is very interesting, i will have to read it again when ive slept ! Thank you for this interesting concept highlight

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Authority:

Health Protection Agency 2010

Health Effects of Exposure to Ultrasound

and Infrasound

Report of the independent Advisory Group on Non-ionising Radiation

Documents of the Health Protection Agency

Radiation, Chemical and Environmental Hazards

Report of the independent Advisory Group on Non-ionising Radiation

Chairman: Professor A J Swerdlow

February 2010

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Facinating. Thank you for sharing. Substacks are great for like minded folks to discuss and chat about out of the box thinking and ideas secular society does not discuss or think about. Very refreshing. 😎☕️

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Karl in your research of science papers do you have any clue of how new the technology you observed in the blood may be? I am pondering that it might not be as old as 5 years or it may be a lineage of technology constantly being updated from the turn of the century.

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I honestly think at this point that even if you find papers that go back 10 years on lots of stuff then you will likely later learn it was known to someone else maybe 20 or 30 years prior when looking deeper. Microcapsules and protocells are said to be a theory still, Unless you look for papers on them and then there they are, papers going back to the 70's at least. really we cant tell how knew it all is, but much of this stuff i think i have seen in papers and by others including myself where morgellons is concerned.

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Hello Karl

the irregularity within the bubbles could come from this process:

I was able to film how a kind of chip has turned into a bubble and in many other bubbles that have these corners, residual structures of it can still be seen inside.

https://sam368.substack.com/p/metamorphosis-of-a-technology

I assume that these chips can either become liquid and produce something and then go back into the crystalline form. What is always interesting here is the fact that a red and green dot - like a plus and minus pole - can be observed. The red dots are apparently process-leading, as they remain and the other dots seek contact with them during various build-up processes and the bases disappear in the process. Once they are gone - the process stops.

With the bubble structures that form around them, as you have shown - could this geometry possibly also act as a bioantenna?

The double membrane of the cells seems to create an osmotic concentration gradient, with which blood cells can be dissolved outside and special substances can be reabsorbed.

When looking at this process, it occurred to me that this mechanism also provides an advantageous opportunity for these bubbles to move, which is hardly the only reason. Video here https://sam368.substack.com/p/parasitic-development-cycle-of-a

Thank you for your work

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great work you having been doing on your stack. Thanks for joining the war. I will have to catch up soon since i am very tired indeed. Maybe you should consider joining our amateur zoom chats with the Micronaughts by subscribing to David Nixons substack. They have good talks, with show and tell. Sometimes a few really interesting faces drop in too, not that the regular guys are not awesome, because they are a great bunch.

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Just a few observations—In the first video, it seems some exploding circles form mini circles afterwards! It also appears that some of them are created out of some kind of cord structure. I was wondering where all the red blood cells are…

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Apologies for the link - it should be fine to open

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Nanodroplet-mediated sonothrombolysis

Nanodroplets (NDs) are an ultrasound contrast agent, which has recently been applied not only for enhanced ultrasound imaging, but for enhanced drug delivery and more recently, sonothrombolysis of retracted clots20,21,22,23,24. Upon insonation with sufficient PNPs, nanodroplets are able to transition from liquid droplets to gas-filled bubbles, which then have similar acoustic properties and behaviors as MBs. Given the small size of NDs (100–300 nm) compared with MBs (1–10 μm), NDs have the potential to penetrate into retracted clots with low porosity. Upon insonation, these droplets can then form microchannels within the clot and act to both mechanically break down the clot via cavitation effects and allow for greater diffusion of tPA and cavitation effects inside the clots20,25.

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