Blood samples—with and without copper shielding
Comparison of Evolutionary Patterns
To demonstrate that the majority of the changes in the blood are related to the radiation to which we are exposed, I conducted an experiment using several blood samples.
One blood sample was collected in the usual manner and monitored over a period of several days, and another blood sample from the same subject was stored in a shielded copper box throughout the entire period.
In the normal, unshielded sample, no decomposition of the blood occurs; rather, a transformation of several structures takes place. This process can currently be observed outside the body.
First, as has been reported on several occasions, the transformation of biological RBCs into synthetic ones. Furthermore, a gradual transformation of the WBCs can be observed, the individual steps of which I describe in more detail here.
Third, cells are currently reappearing in fresh blood that cause the rapid decomposition of a large proportion of the blood cells; in my opinion, this is used for rapid iron extraction,
So, on the one hand, we have components in the blood smear that are completely dissolved within a few hours; this portion accounts for about 1/20 of the microscope slide.
The other portion completely transforms into synthetic cells—recognizable by their extremely thick cell walls and their uniform size. As has been reported several times before.
Here’s a blood test result that looks pretty normal, even though every blood test these days seems to show something that doesn’t really belong there.
Immediately after the blood draw, white blood cells (WBCs) are usually perfectly round—a state of shock-induced rigidity. This should subside after a few minutes, allowing them to resume their normal function. If they do not, the term “lazy leukocytes” is used, although I consider this a misnomer, since they are not lazy—rather, we are dealing with an immune system that is not functioning properly.
The following are the cells that cause massive destruction in the blood count as soon as they appear and burst:
The area surrounding this cell then quickly dissolves—unlike the other cells, which look like this after 5–6 days:
Let’s look at the changes in white blood cells over the course of a week in a complete blood count. Normally, the blood cells should break down, and after 3–5 days, nothing should be visible anymore.
That is not the case here. Unlike the blood sample that was stored in the copper box.
I think the results are clear.
Let’s move on to the scientific studies that point to specific changes in white blood cells.
Leukocytes are already being genetically modified.
Neutrophils and their elastase are of particular interest in this context.
Neutrophil elastase (ELANE) is an enzyme released by neutrophils.
Researchers are now using ELANE in several ways: first, for nanoparticles that are activated only where neutrophil elastase is present, such as in inflamed tissue.
Nanomedicine platform for targeting activated neutrophils and neutrophil–platelet complexes using an α1-antitrypsin-derived peptide motif
Or artificial nanosystems that mimic the tumor-killing effect of elastase.
A neutrophil mimicking metal-porphyrin-based nanodevice loaded with porcine pancreatic elastase for cancer therapy
And let’s not forget the CRISPR-based approaches that specifically modify ELANE expression, for example, to treat congenital neutropenias or, experimentally, for tumor therapy.
Targeted inhibition of ELANE expression using adenine base editing to treat severe congenital neutropenia
The idea behind this is that elastase can be used as a biological “switch” or as a therapeutic tool.
Eosinophils are particularly interesting in this context. Eosinophils do not possess eosinophil elastase. This is often misunderstood.
Instead, they contain characteristic granule proteins such as:
Eosinophil peroxidase (EPX or EPO)
Major basic protein (MBP)
Eosinophil cationic protein (ECP)
Eosinophil-Derived Neurotoxin (EDN)
These molecules are used to combat parasites and play an important role in allergies and asthma. This could explain why, in blood tests lasting days or even weeks, no bacteria or fungi grow in the specimen—a normal occurrence in purely biological samples.
Eosinophil peroxidase is already being studied as a biomarker, a drug target, and a potential tool in biosensors.
Leukocytes can also be used as “living nanorobots.” For example, nanoparticles are attached to leukocytes so that the leukocytes can transport them autonomously to tumors. Alternatively, the cell membranes of neutrophils are used to make nanoparticles “invisible” to the immune system.
That’s exactly what I demonstrated in my first video—the complete construction of a quantum well camouflaged by eosinophil peroxidase
Even though most of you are probably already familiar with it—here’s the video again
Most recently, artificial neutrophil-like cells have been developed to mimic chemotaxis and bacteria-like defense functions.
Engineered Artificial Human Neutrophils Exhibit Mature Functional Performance
In summary, this means the following
Leukocytes are already the subject of intensive research for applications in synthetic biology and nanotechnology. Neutrophils and their elastase (ELANE) have been studied particularly extensively. Eosinophils are also the subject of research, though more for their specific granule proteins—such as eosinophil peroxidase (EPX)—than for an elastase.
The latest research focuses on programmable immune cells that act as “living robots,” DNA origami on leukocytes, and cell-based nanofactories or synthetic granulocytes that are produced entirely artificially.
Here is one of my remote viewings on this topic from early 2023
It shows exactly the process that I was able to detect in the blood six months later.
We can clearly see in the blood that all of this is not just a pipe dream. To observe this process properly, it is important to let the blood sample sit for several days, rather than just observing it shortly after collection and discarding it immediately. The effects only become visible after a few days, though some samples survive for months.
This can currently be observed outside the body. The extent to which this development eventually occurs within the body is likely a question of the immune system and its functionality.
Finally, here’s a video of my Future Targets—subscribers to my channel also get access to my website, which is primarily about remote viewing. And the Future Targets aren’t just there to see the future—although that can be quite practical—they primarily serve as a test to determine the accuracy of the hit rate. This is because sessions designed to examine changes in the body or the effects of medications should be as precise as possible and yield reliable results.
SAM
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