Parasitic development cycle of a technology Part 2
Too complex to serve merely as a weapon... - right?
This is a war in our body
Continuation of part 1
Let's take a closer look at these "bubbles"...
The following descriptions are all based on observations - so they may or may not be correct... Please bear this in mind when reading these articles
After hours of sitting in front of the microscope, you will find anomalies and avoidable correlations like this one:
At the beginning you almost always have the feeling - hey - the blood looks somewhat "normal", if it weren't for this often appearing strange transparent film that covers some parts of the slide. This can be recognized by the border and the need to readjust the focus.
If you look closely, you will notice small blurs that look like small tornado structures.
If you observe this over a longer period of time, bubbles suddenly form in the field of erythrocytes, which then produce this strange symmetrically arranged image
These blisters then begin to grow. What precedes this is the rim that forms around these blisters - where there are no blood cells. Is toxic fluid leaking from there?
More bubbles form inside the blisters, which grow larger over time and burst in repeated cycles.
The blood cells around this large bubble lose their red color and fade until they begin to dissolve.
Inside the large blister, further blisters suddenly appear, which are bounded by a membrane. Gene-like structures now grow on the inner edges.
And at the same time you think - this technology is laughing at you...
I suspect that this double membrane that is created here generates an enormous concentration gradient, with the aim of creating a suction from the outside to the inside and thus creating the highest concentration inside to produce this gel.
And once again, our red blood cells serve as the substrate for the whole thing.
It can then be observed that the bubble structure opens - in order to release this new structure to the outside.
However, that's not the only thing these cells can produce. They also seem to produce these black cells that look like a squashed mushroom head.
This is what they look like in the blood:
These cells are extremely toxic to cells. Whenever they appear, the blood disintegrates at lightning speed. It doesn't take a day until the blood sample on the slide is completely destroyed and no further statements can be made.
I was able to make the observation on various test subjects that these toxic cells appeared shortly after taking a few days of methylene blue. You can't help but see a kind of intelligence in this system, because with the methylene blue you cut this synthetic biological technology off from its food, the trivalent iron. And that's exactly when these cells appear to provide replenishment.
To counteract this, we have switched from taking one dose of methylene blue per day to two doses 12 hours apart. At the same time, we are currently using sodium citrate for elimination.
The following article is about breaking up hydrogel structures in medicine to transport stem cells. In this study, a combination of EDTA and sodium citrate proved to be the best combination.
Optimization of agarose–alginate hydrogel bead components for encapsulation and transportation of stem cells
It is not easy to get a real sequence of development in this somewhat complicated overall process. There are several processes that take place simultaneously and activate different sequences depending on how they are controlled by a frequency.
As written in the last post, not only further developed "blueprints" appear - but also new types of strands.
And these look very similar to normal technical cables.
But these "cables" can also be excreted in the urine...
At first they were only visible as very thin strands - and now they form complete, clearly defined lines inside, and at the ends a growth or a kind of "docking point" is clearly visible. The only question is - how?
This technology in our blood is enormously complex.
It assembles itself independently. It reproduces and repairs itself and reacts like an intelligent organism to interventions in its development cycle.
We no longer have time to wait for someone else to offer us a solution. We all need to throw our observations and knowledge into a big pot and exchange ideas.
We need solutions and each of us is needed.
Wish I could be of more help. I’m only able to see the ribbons’ in the live blood. All samples have them that I have observed . Scope I obtained a few months ago on the cheap . Your observations here and suggestions for the behaviors are great and I hope can provide helpful insights into how to cope/deal with this invasion of natural biology.
I’ve been following David N. Matt , Karl and Scripio . Just this past week I’ve connected locally with a Chiropractor who is interested in learning and has an old dark field capable scope .
Have checked Urine after SC . Being rather green at this I can’t tell what I’m seeing but an increase of ‘crystal’ structures and busy ‘dots’.
Big fan of the late Royal Raymond Rife and his successful work with frequencies.
Thanks for your diligence.