Has another patho physiomorphic mechanism been discovered that underlies Morgellons?

A wide variety of stages of transformation

You’re sitting at your microscope and once again come across these cells that look like yeast cells but behave like spores. All emerging from a giant hydrogel mother ship.

“Not them again,” you think to yourself, like those impenetrable membranes from the Fort Knox article.

This preparation is derived from nasal secretions containing what is known as Saharan dust.

Let’s take a look at the first stage

I’ve now used different microscope slides to see how they react

One was left outside in the sun, and one stayed on the microscope

Images from Group 1: On the slide that was left in the sun, almost all the cells had broken down, leaving behind these small rod-shaped structures.

Images, Group 2: The slide on the microscope has changed in that the cells began to form vesicles. The more light there was, the more pronounced the change became.

The images are very reminiscent of our WBCs, which try to break down clots in the blood and in the process are completely destroyed themselves—they have the same appearance. Here is one of the photos:

The “bubble portion” keeps getting larger, and the actual cell residue is pushed to the edge.

And this is what the sample looks like after another day: Only large bubbles remain—exactly the same bubbles that appear in the blood—and they are still referred to as air bubbles.

The area, with all the released substances, now looks like this:

We are also familiar with these round, self-assembling structures, which look like individual components, from the blood

We’ve seen all these blisters before, and under frequency stimulation, these blisters develop into fibers—Morgellons, or whatever you want to call them. Here, you can also clearly see how the chemical activity within the bladder is taking place on the side where the thread has formed.

And we know them in every color, from clear, pink, blue, and yellow to brown and even black.

Hydrogel production is now starting up again inside the bladders—which then form a second inner bladder, just as we have seen in previous years.

These filaments, antennae or Morgellons can be transformed back into the hydrogel phase.

Here are some pictures of Maria Crisler, who was able to reverse the process with the help of PEMF. The round bulge is the thread becoming liquid again.

To avoid misunderstandings: The filaments are created from the bubbles by frequency pulsing.

If they continue to be exposed to PEMF cycling over a long period of time, material fatigue occurs and they begin to “leak” again, as can be seen in these pictures.

© Image by Maria Crisler

© Image by Maria Crisler

© Image by Maria Crisler

© Image by Maria Crisler

© Image by Maria Crisler

Summary of current findings:

We absorb these large cellular units from the air—and thus also from the water—which then release a further subunit possessing a yeast-cell-like wall and a distribution pattern resembling that of a spore. Under the influence of light, these cells transform into independent bubbles.

If there are multiple cells in the vicinity, the whole assembles into a larger bubble structure.

When these bubble structures are exposed to frequency intervals, either the fibrous structures—some of which are known as Morgellons—begin to form, or additional hydrogel structures form inside.

The individual released cell units bear a striking resemblance to leukocytes, which attack these fibrous structures in the blood but are unable to phagocytose them, instead perishing in the process. The chloride released as a result is used for the construction of the exodermis and battery units within the body.

The chloride is bound to the rhodium, which is currently present in far too high a concentration in the body. This appears to be the reason why, for over a year—actually, almost two years—we could no longer detect any chloride under the electron microscope. So where did it go? It was incorporated into structures.

Since the combination of Novalytic, lactoferrin, Insulsess, and, in some cases, Artemisia annua, it has reappeared, which suggests that the structures that have already formed deeper within the tissue can be broken down again.

Here’s a word about CDL—chlorine dioxide.

If someone takes CDL and the chloride is no longer detectable here either—where has it gone?

Chloride is used in nanotechnology for the entire battery and power grid industry—and an important example can be found here:

Aqueous dispersion of carbon nanotubes by chlorine dioxide oxidation

The targeted oxidation of CDL on nanomaterials makes it possible to bind various materials that are specifically used in sensors, catalysis, and biomedicine. In other words, CDL prevents sticking and clumping. Chlorine dioxide is specifically used for the oxidation of carbon nanotubes (CNTs). It is also a very efficient agent in UV processes, which brings us to the control frequency of nanotechnology. CDL is specifically used to modify materials in nanotechnology.

So I can’t say that CDL is a panacea. Especially since we have massive rhodium exposure.

Chloride is bound to rhodium, among other things. All the chloride is extracted from our white blood cells. If I use CDL continuously, the process will likely proceed more quickly.

Sorry if I’m being a killjoy again—but there is currently no panacea for what’s going on inside our bodies. It’s extremely important to look closely at exactly what each substance does in the body.

This is what better water solubility of carbon nanotubes looks like with the help of CDL.

And it is a classic nanoeffect caused by CDL: Minor chemical changes completely alter the behavior of the material.

If an ordinary person is expected to navigate this whole maze of treatments and mechanisms of action—I know it’s not easy. But it’s important to do your own research.

SAM

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