Different hydrogels - different key frequencies

Addendum to the post - Green Laser

To get straight to the point - we show phenomena, reactions and changes that we find in the blood count. Sometimes they are desired - other times they are not.

We will not offer any cures - we collect information and exchange information internationally across the globe.

Back to the green laser based on this post:

After several experiments and reading all kinds of scientific articles, the 530 nm seems to be one of the key frequencies for controlling synthetic technology.

However, one frequency alone is usually not enough.

530nm is the information that ensures dismantling or dissolves the cross-linking of certain hydrogels, perhaps it simply represents a stop switch for some functions.

Only when the door to a hydrogel or molecule is closed - this command is only weakly or not executed at all.

I have carried out several tests - and Matt and Uli are also in the process of investigating this possibility. - Thank you guys :-)))

Example:

A blood sample without methylene blue staining and irradiated with the green laser allows the process to proceed much more slowly than with staining.

Not all hydrogels respond to this frequency either. They are only those that have a productive function or can release substances into the body.

Here is a picture of a “cluster” that produces these round cells - after irradiation with a green laser, it slowly expands and holes form in its structure. It doesn't dissolve as quickly as with methylene blue.

Before laser irradiation:

(I know that in the dark field literature this is viewed as a large mega platelet, but this one definitely produces round, new cells.)

After 3 minutes of laser irradiation (532nm green): The reflection of the tissue has decreased, it has become slightly larger, but not comparable to the observed dissolution process as shown in the post above.

However, there is also a frequency in the blue spectrum that activates and accelerates all production of synthetic technology. It acts like a door opener. This can be permanently seen under the dark field microscope. When the LED light source in the microscope is switched on, the synthetic structures grow much faster than when the light is switched off. And LED has a high blue content.

Ergo, we need a blue frequency and the green laser in combination to get an effective result. Methylene blue absorbs visible light in the range of approximately
530 nm to 700 nm; the absorption maximum is at 660 nm.

Tests with normal filter disks in different shades of blue and the green laser also did not show the desired result. And without a laser - only with green and blue color filters - there is no reaction at all. So there has to be a concentration of light - and thus a targeted triggering of a reaction. It's best compared to a key that has to be inserted straight into a keyhole - it doesn't fit at an angle.

This concentration of blue and green must come together to trigger the effect.

It therefore looks as if the correct “key” consists of two frequency waves sent at the same time and there is then an immediate reaction at the receptor.

In the case of triple-crosslinked hydrogels, there are even up to three frequencies that lead to dissolution.

Green 530 nm - Blue 405 nm - which is almost UVB range for TTET processes - red with 617nm or 635nm.

As with UV light irradiation of the blood - where blood is taken, irradiated with UV light and immediately reinjected again, there is a possibility of reproducing this principle with other light irradiations.

We continue to research.

And I am grateful for everyone who pursues their own research here and makes it available to the public. Many approaches from a wide variety of specialist areas lead to new insights and solutions.

Thank you all!!!

SAM

www.darkfiel-enigma.com