What more evidence is actually needed?
Another remodeling of our immune system
Another attack on video, how our immune system is utilized in the blood. And if you really understand what is happening here, it should be clear what kind of problem we are really facing.
A chronological sequence for understanding:
Bubble fields - as I call them - have recently appeared in the blood count. Areas where the blood is covered with small bubbles that are completely black on the inside.
In addition, bubbles appear that are more reminiscent of mushroom heads, slightly shimmering in a mother-of-pearl color. Like in this picture: In different sizes
I then took a picture every 10 minutes to see if there were any changes. The cells were suddenly in a completely different place. However, no movement was visible to the naked eye. So I filmed the process and then sped it up.
And sure enough, something was permanently protruding from under the cells like an amoeba and moving forward. The similarity with the way in which leukocytes move is unmistakable.
Here is a movie taken 10 times faster (1000%) so that the process can be seen at all:
They also specifically target other bubbles, absorb them, but then release them again without anything. A normal leukocyte would not do this. Unless it would not recognize them as foreign.
The round structures awaken and become so large that it is hardly recognizable that something underneath them is causing their movement.
A movie of a cast cell at original speed - to see the process you have to activate fast forward or move the slider forward quickly by hand.
It is striking that there are no normal leukocytes around these fields. This gives rise to the suspicion that it might once again be a remodeling process of our cells.
So we start looking. And sure enough, I found this leukocyte moving at normal speed that had phagocytosed a small bubble and a larger bubble and was dragging them along.
The leukocyte has definitely recognized the round blister as foreign and wants to eliminate it. However, this does not seem to work, and this new guest piggybacks along the whole time and feeds on what the leukocyte absorbs. At the same time, however, a kind of reprogramming must take place, because other round structures are still taken up afterwards but are all released again. Over time, this foreign first sphere grows and becomes larger and larger. And our leukocyte becomes slower and slower, but continues to do its work and thus continually feeds the parasite.
I cannot yet say what will become of this cell in the course of time. The only fact is that we are once again dealing with a new type of remodeling of our immune system. And everything that our immune system recognizes as foreign and tries to eliminate is recycled by this cell. In addition, it has camouflaged itself in our immune system and is therefore no longer vulnerable.
WHAT ELSE DOES IT NEED?
Let me briefly summarize what I have found since mid-December 2023
Cells built from leukocytes that build chip-like technology camouflaged inside
Direct attack on our red blood count
Chip technology that can dissolve - and release medication
Building giant cells - to produce whatever
Reconstruction of Leukos and reproduction of synthetic technology
Synthetic blood cells that do not rot...
Release of nanobots through fibers and activation of 0.9% salt
And now this process here - apart from all the fibers in whatever form and the liquid bubble stuff, although in the following picture I assume that these are bioantennas.
And not forgetting the different strands, as seen in a few in this post, which appear to be something like blueprints as they are read by the technology.
But dark field microscopy is not scientific - because the light comes from the side and not from below. Let's continue to kill everything and try to detect living processes in the dead state. Schizophrenia to the power of ten.
And last but not least, an AI that will take over the entire system, as our nerve cells now have built-in piezoelectric crystals made of barium-strontioum-titanate instead of copper and can be controlled directly.
Great thought provoking work, I don't have time to read all other articles tonight. I will in morning.
What is happening is beyound words. Biblically end times.
Keep going chelate as best you can, then replace the chelated heavy metals with Copper(ii) Glycinate, you can get it from Naturopath. Copper(ii) glycinate is also a weak chelator. Use Vit C, green tea all the chelators you can get hands on...replace minerals with supplements...
Block the ACE2 receptor as best you can, using hesperidin, eggs, CBD, and Curcumin.
If people know they have wriggily white clots, use green led laser, to open up the drug delivery mechanism. This helps let the in the chelators to break up the nano heavy metal linkages...
I need to write big post on phone... The above is what worked for me. 💙🧙
I think the smaller bubbles are being "nursed" or fed by the larger leukocytes (?) which contain the "milk" or nutrients the smaller ones need to grow and mature. The nutrients are the nutrients our RBCs carry to our own cells. I've witnessed this over time in my own body.
Of course, I may be wrong, but when I view your first video, I see a kind of proprietary "care" for the smaller bubbles by the larger and as I said, I've witnessed the growth of smaller organisms into much larger ones over time. Like "baby bees" in the honeycomb being fed and incubated.
Thank you so much. Your work is illustrating the mechanisms they use. Somehow I have a feeling if we can find a way to disrupt the mechanisms they will die from malnutrition.
Soon I am going to try a prolonged fast to see if I can starve them. When fasting, as I understand, my cells, especially the RBCs, form a protective layer to prohibit the loss of nutrients from inside them. Perhaps this protective "skin" or "layer" can prohibit the tech from feeding?
Basically like starving a vampire or other parasite.
Forgot to say I also seem to see harvesting by the large "leukocyte" of the RBCs as it pushes through them. The "dots" seem to be breaking the RBCs outer membrane for ease of access by the "leukocyte" for future harvests?
If the "leukocytes" have been repurposed by the tech, this may explain, in part, why people's immune systems are dys/nonfunctioning. The "leukocytes" are no longer hunting and destroying foreign bacteria/invaders to the system and this allows infection to run amok.