Microscope Journal

These experiments were done in vivo on my body.

Please refer to this spreadsheet for the experiment methods. Please refer to notes and positive results in the same sheet for detailed explanations and hypothesis.

As I become more experienced with blood and blood artifacts I will be able to better identify methods for manipulation. This is far from ordinary in the modern biological context. These results were obtained using methods not present in current biological physics, and it is necessary that you comprehend the subjects within this website in order to understand why this works on a physical level.


First measurements of apoptic behavior

Thursday, March 28th 2019 - First measurement of apoptic behavior (⎍ LH(18)428 (Static) T(16)118.5)

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Friday, March 29th 2019 - Allowing the system to rebalance (No sessions)

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Saturday, March 30th 2019 - System has reached a balance (No sessions)

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Points of interest:


Diet

I will be keeping my diet generally restricted to these items so as to ensure as stable as possible a level of results

Because it is likely this concept is going to become adopted as a standard in later years, I am removing meats from my diet.

I do not wish for any animals to be specifically sought after for the sake of an individuals personal gain. Eggs were not removed, because there are humane ways to raise and cultivate an egg from a chicken. They also are a prime source of sulfur which is needed. As is protein. I may come to remove eggs as well as I learn which foods can be better substituted.

2-3 Eggs with butter

1 Piece toast

Peanut butter

1 Apple

Milk

Vitamin C

Vitamin B12 (when states of apoptosis are high)

Greek yogurt

1 Piece toast

Protein Shakes (on occasion)

I also drink on occasion or diverge from the diet, but the overall is within these parameters. It is also intended that a way is found to do these types of things without too much worry towards diet as long as some specific needs are met.

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Replicating results

Everything has re-balanced to a relatively typical state; can enable apoptic behavior within about 30-50% range within 1 hour 1 session. Experimenting with different frequencies at end of day to see if any reduce amounts. Seems that some do, but need to see more results to show this.

Sunday, March 31st 2019 Morning (After) (⎍ LH(18)428 (Static) T(16)118.5) - Used KHz & Hz

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Sunday, March 31st 2019 Night (After) (∿ HEME(6)644 (Static) CValue540) - Used KHz & Hz

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Cells have already reset

Monday, April 1st 2019 Morning (Before)

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Monday, April 1st 2019 Morning (After) (⎍ LH(18)428 (Static) T(16)118.5) - Used KHz & Hz

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Monday, April 1st 2019 Night (After) (⎍ LH(18)428 (Static) T(16)118.5) - Used KHz & Hz

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Some significant changes seen today after first session. There were some enlarged phagocytes to such a degree that it required multiple images to capture the entire structure. There are also dislodged tissues. I am hoping this is scar tissue from a site I have been affecting purposely, will see. I plan to continue this for at least a month.

I am learning how to calibrate my microscope to give this a measurement but have to purchase a calibration slide first. I’m not sure if I will have any money left to do that, so it might have to wait.

Points of interest:

April 3rd – 3 videos of movement observation. One in open space, one confined healthy – one confined apoptic.

Wednesday, April 3rd, 2019 Morning (Before)

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Wednesday, April 3rd 2019 Night (After) ⎍LH(/1)7704 (Static) ⎍T(/4)474) - Used KHz & Hz

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Friday, April 5th, 2019 Night (After) (⎍LH(/1)7704 (Static) ⎍T(/4)474) - Used KHz & Hz

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Not a whole lot is different besides some noticeable structures showing up. Cells still reacting the same way. It has become apparent that apoptic behavior is not just cell age, but due to structural integrity as a result of its electromagnetic capacities. The cell will loose stability, and become apoptic as sugars deteriorate and other portions of molecule chains begin to fall out of sync. This happens over time as pieces are pulled and the cell is pushed and tugged on. Apoptic cells tend to congregate together and away from healthy cells – as opposed to intermingled/without reason; which is a clear indication of pressure stabilities and the cells capability to follow the whole of the body. They are often found towards the ends of the slide where healthy cells will gather in open space and towards the center. This reminds me of the “skin effect” in electricity; which is also pressure reliant.

It is incredibly time consuming taking pictures of my blood 4 times a day, so I am going to stop taking as many images, and stick to only taking blood after the night session unless something drastic changes.

Points of interest:


Rebalancing Systems & Modulating Cell Size
Documentation

Monday, April 8th 2019 (∿ LH(1)15.38Mhz (Static) ⎍T(4)3.764Mhz)

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Nothing much changed visually here, and I am still waiting on the calibration slide I ordered.

April 10th (∿ LH(1)15.38Mhz (Static) ⎍T(4)3.764Mhz)

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Most recent visualization.

April 11th (∿ LH(1)15.38Mhz (Static) ⎍T(4)3.764Mhz)

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I will continue to document changes. As soon as I feel the cells are stable and consistent I will start to use Hz values again to see if the cell sizes increase.

Points of interest:

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