The methylene blue dilemma

We need to talk... and prove...

This article is getting longer - long to be precise. Light fare is something else...

Firstly, I am amazed that my article on synthetic blood cells has made such waves, because after the neoplasms I have found and published in the last few months - the detection of synthetic blood cells was only a logical consequence.

But from the beginning. Let's start with the use of methylene blue. On the one hand, it is used to stain the preparations, which has worked well so far. Until the first oddities appeared in the last 2-3 weeks.

So far, methylene blue has also been a good support in the conversion of trivalent iron into bivalent iron and thus a good support for the body in the excessive destruction of its own blood cells. It also seemed to reduce the activity of some hydrogels.

This has changed. We have different types of hydrogels or filamentous structures in the blood that react completely differently to methylene blue.

I have a blood sample here in which the interaction of various factors can be shown very well. Sample stained with methylene blue, as otherwise the effects that occur are not visible.

At the beginning are these cells, which have been observed to have a very blood-dissolving effect as soon as they open. When you find them, you know that hemolytic processes are about to occur.

1 Fungus-like cell

This releases a lot of iron from the haemoglobin - which leads to tiredness, loss of performance and sometimes headaches. At the same time, these cells are present, which use this iron to incorporate it into synthetic blood cells, as I assume:

2 New cell formation

Methylene blue is a good choice to bring a wedge into this production and the process. The filamentous or hydrogel structures that are present at the same time also stain strongly and it seems or appeared that we had found a good therapeutic approach here.

However, we now have the following almost cable-like structures, which have become increasingly common in recent months:

And now the same structure 2 hours later

With all other hydrogels, this type of crystallization is not observed in the presence of methylene blue. Not even the next day.

3 Hydrogel without change

4 Hydrogel without change

Similarly, the next day several new spiky structures form near this cable-like structure, such as the following:

5 New crystallization

6 New crystallization

7 New crystallization

Now you could say - methylene blue alone also forms long crystal structures - but here in the blood count they only form on this special fiber structure.

A few months ago, these structures still looked very small and were more in the background - as can be seen here:

8 Initial cable-like strands

Since, according to the Carnicom Institute, methylene groups are also used by this nanotechnology, the property of methylene blue could be used to build precisely these linear structures.

So is methylene blue helpful or not? It's hard to say - and internal intake should be carefully considered. And the saying - the quantity makes the poison - unfortunately does not apply here. It only determines whether growth is slow or fast.

Is taking methylene blue good or bad? Everyone has to decide that for themselves. I would then insist on examining the blood count permanently and at regular intervals by dark-field microscopy in long-term observation with methylene staining - so that nothing gets out of hand here. At the present time and from the point of view of nanotechnology, however, I think it is Russian roulette, at least what I see here in the blood.

In this context, I would like to refer back to my first post. It shows how a chip is built in the bloodstream, where material from our defense cells is used as a protective shield. This is exactly where I would have expected an outcry, because it shows what is needed to implant something like this in the body.

We need a system like this:

1. A programming code in the form of RNA for the reprogramming of our cells - this can enter the body via viruses, bacteria or the other methods we are all familiar with.

2. A production facility requires the necessary materials - which we can ingest via water, food and air or modified vitamin preparations and medicines

3. A start trigger - which runs via frequency technology - various towers, cell phones, etc.

4. Coordination of the system through artificial intelligence.

5. Mutual communication and control mechanisms

6. Logical and goal-oriented thinking that anticipates and reacts to various countermeasures

If we were initially successful with Mehtylenblau against this technology, we may now have simply adapted and reprogrammed it. We are dealing with an intelligent system that reacts to our measures. And it has the advantage over us that it knows exactly what its goal is, how it works and what happens when, and is therefore always one step ahead of us.

Not good.

Here again a first video with the production of this chip. Right-angled structures do not occur in biology. In the crystal kingdom, yes - but not in blood. For my part, I was speechless in front of my microscope for the first time during the observation.

But back to the blood picture above. Here is a picture where you can clearly see two different types of blood cells. At the bottom left, the regularly shaped ones with thickened walls and diagonally at the top right, blood cells with thinner and deforming walls.

9 Different appearance of the red blood cells

Here is a detailed look at the individual blood cell fields

10 left area

11 right area

I think the difference is very clearly visible.

Another strange occurrence occurred at the edge of the sample. After about a day, quantum dots began to swarm here.

They weren't available in these quantities the day before.

Where did they suddenly come from? When exposed to light, the hydrogel usually spreads and expands at the edge - and in this case it is still mixed with methylene blue... And it slowly makes you feel uncomfortable...

The absence of crystal-like neoplasms is also visible in this area - they can only be found in the area of the cable-like structure.

I can only call on my colleagues with a darkfield microscope to check these tests to see if they come to similar results.

Since different characteristics are more or less in the foreground from continent to continent - other reactions could also occur elsewhere - and if someone asks me now what I would like - then quite clearly

A mass spectrometer.

Working only with a microscope will sooner or later bring us to the edge of our possibilities.

And now some more pictures - all from the same blood count, which I will definitely be observing in its development over the coming weeks, should it not disintegrate.

I already apologize for not being able to reply to everyone's comments, or only after a delay - as there is quite a lot going on.

12 Hydrogel with fungus-like cell

13 Large hydrogel block

14 Neoplastic production

15 Gel structure with defense cell

16 Neoplastic production

17 large Hydrogelstructure

18 “small” Hydrogelstructure

19 Cell change unknown to me

20 different cell types

21 Hydrogel with stained dot units

22 Hydrogel

23 New formation - but of what?

24 Fine fibers or threads

25 different RBC's

Finally, I should perhaps mention that this blood count looked completely harmless a month ago - as far as one can tell from today's blood tests.