Hydrogen Peroxide added to blood reveals highly concentrated amounts of the technology.

At this stage i feel sick to my stomach, On the bright side the new camera is clearly amazing on the Leica DM2000 scope!

Testing Hydrogen peroxide further and adding a drop to the side of the slide has only disturbed me more. Images taken with 25x objective, Dark field.

While the Hydrogen peroxide certainly DOES disfigure the composition of this material, and strip material from the blood, it also separates much of the material from the blood plasma and outside of the RBC’s. Unfortunately even blood which looks of reasonable condition by today’s standards what is clear is that the amount of undesired material present is still in shocking amounts. I will bullet point my observations below the image of my blood taken before H202 addition.

My unvaccinated blood with mostly white cells and very little debris showing in the plasma, looks good right ? 25x objective.

Examine all of the images in this post carefully on a big screen to get a better understanding of the visuals.

My observations:

1. H202 disrupts the structures and material rapidly.

2. The material that is separated tends to concentrate away from blood and closer to the H202 application site after some time.

3. The material begins to try reform and many different structures can be seen after the H202 has dried up or expired.

4. Fibers, droplets, gels, coacervate like structures, and colorful dots appear very densely.

5. Some of the blood could now be seen exposing the colors of the dots inside the RBC’s. We have been seeing these nodules clearly across the globe and now having much a better microscope and camera i can see this dot phenomena enough on my big screen here. See blown up image below.

Affects of H202 on the dots seen in cells are not noticed if there is any affect at all. This is unfortunate

The clarity is not high enough on smaller screens, I viewed this on a 23” monitor which you can see the details on clearly enough.

Enlarged image detailing colored dots in the cells. It is the H202 application after a short time that allows the cells to expose these details.

I have a curiosity as to whether or not blood letting will allow the cells to be replaced by new ones which have none of this material inside. If not then it would be even more concerning that new RBC’s could be formed with the undesirable material inside of them already for obvious reasons.