Molecule Syncopations

These were determined using Binary Values here:



Molecule Linking (Creating More Rational DNA)

For reference, this is what a real strand of DNA looks like at a distance

DNA De Sync – Adjusting DNA properties

Alternate DNA recreation (VST)

Rudimentary Hydrogen Chains

Double Helix Recreation 2

Please note the frequency values; 360 hz (circle), when using 2/3 type voltage. Evening the values out brings frequency high to 528 hz. Unironically this matches the solfeggio DNA value.

Double Helix Recreation 1

Wave Syncopations

DNA Wave Syncopation

General Wave Syncopation

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Binary Pyramids

This is what the Periodic Table looks like translated into binary values (per element). This is only 26 elements in: up to Fe (Iron). Zoom in and out here to get a perspective (in the sheet labeled “Binary Pyramids”).

A massive question is now brought to the table of what the ethics surrounding these values mean. As of today, we have officially developed the capabilities to simulate that of a complete universe. This requires a total shift in the way we see things.

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Rebalancing Systems & Modulating Cell Size Through Electrical Current & Apoptic Behaviors

Please reference pictures for recent results in cell modulation below as needed:


It is now hypothesized that this method can be improved upon and added to in order to completely reform or repopulate an environment of cells.


This is a second step in a series of experiments conducted over the course of the past 4 months.


As determined during apoptic behavior in my previous study / results, cell states are enforced upon by the vibrational rate (frequency) of the introduced current; or in other words, size is restricted by the rate at which a current is oscillated, which is a factor of capacitance or allowed space.


If the threshold for a cell is breached in a stable and consistent manner it will die or divide. Upon death, reformation is possible.


Previous hypothesis:

With relation to self regulated apoptosis as a result of the introduction of current; it had been hypothesized upon findings and within the bounds of variable cell theory that the matter of blood (cells) is strictly an outcome of two – to many point differences upon a wave (pressure) and as a result of time; frequency.


These findings have been expanded upon:

As hypothesized to now prove the regulatory capabilities of the size of cellular structures, and that cell size by frequency will have a limit. Due to correlation between these binary ratios: link. It is also hypothesized that these findings will be replicable by reducing frequency.


As frequency is increased, allowed space is also decreased; resulting in smaller cells. As frequency is decreased space is increased between wave positions; resulting in larger cells. Due to scalar possibilities, there are thresholds where these rules are hypothesized to invert. Those thresholds are still yet to be determined.


The cell combinations to form molecules are variable as a result of this, and smaller cells may result in capabilities for growth due to spacings and allowance; along with alternating pressure. Larger frequency rates (longer waves) are likely to result in smaller molecules if a structure is already formed, as the structure will be required to adhere to the wave, and if it is not large enough already will be enforced upon to react and find ways to fit into this instructed state. This is already seen to happen in males if testosterone levels are too high, and the testes shrink.


A modulation between the two frequency states and cell sizes over time may influence cells to enact specific behaviors. Besides the growth and size reduction in both Red Blood Cells (RBC), and Phagocytes which I have documented; those behaviors are also yet to be determined, and will require more study along with replication of results, some of which I will be able to determine in the coming weeks.


I am also beginning to find that some wave forms seem to affect cells more effectively than others. Square waves for example (100% on 100% off – not to be confused with duty cycles) seem to enable apoptosis at higher rates, likely cause is there is no slope contained in a square wave. Sine waves are expected to result in better buffering or over-all less invasive technique.


This was the first noted change in cell sizes. It has been found that smaller cells will gather outside of larger cells; apoptic cells will gather outside of healthy cells, and healthy cells will gather towards the middle of each slide and in places with more space. Sometimes visually healthy cells appear to become apoptic within about an hour of spending time in a confined space indicating again that this is a result of cellular and environmental pressures; where the instability becomes apparent without movement, and the cell itself was not stable to begin with.


These images are all taken immediately after blood withdrawal. It is very difficult for me to show what I am seeing as the microscope I am using has a very short battery span, and terrible storage. Now that I know what I am looking for I will be able to better document the changes, but there were points where the cells which were clustered were just fractions of the other cells in size. You can see this yourself in the images. Often they were embedded into the larger apoptic cells as shown in the video on April 8th.


This was the first indication of cellular size differences, which took place after 2 weeks of documented apoptic behavior. It is possible that it is first required to reset or “reboot” the system via cell death in order to instruct the cells to build at a different size. Or at the very least that apoptosis will aid in the frequency at which these changes occur.


Images 100-004 8th is where this is visible. I also found that within days Phagocytes were no longer exponentially enlarged and reduced to regular size. You can see these changes over time in comparison to the previous pictures found in Microscope Journal.


Take note to Phagocyte size in relation to RBC changes.

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


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)


Most recent visualization.

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



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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How to calculate the circumference of a circle without using Pi. — The ratios behind cell division and atom creation.

This is Ratio Math, which relies only on fractions of objects to calculate objects. Just like Pi, but more tangible, as the numbers are themselves derived by the circle, and are not random, but wholly circular.

Tl;dr this is the formula:

44 * 360 * 4 / 7 / 8 = 1,131.42_875142_875142 like Pi is a tangible circle ratio, only this ratio repeats itself (just like 22/7).
This is a very specific value.

Divide any circle diameter by 360 and multiply the value by 1,131.42_875142_875142
This gives you the circumference as a value of ratio to the physical decimals followed by the circular value of 857142.

For example, π * 44 = ~138.23
This gives you 138.2_857142_857142

It works for all other values, as long as you use the rule of 44 * 360 * 4 / 7 / 8, and Diameter / 360.

It provides an answer as a ratio to be used for long term; or high value ratio calculations as perfect ratios. The value 857142 is not to be seen as a number, but that of a ratio (circle). I am still working this into ways to bring the numbers up or down for exact measurements and locations, but I wanted to share this now, because I am already finding many links to this and the ratios of cells, vitamins, and DNA.

This explains how cells divide and atoms formed. I have a somewhat tangent based explanation of it on the right side of this sheet, which I used to figure this out.

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Microscope Journal

These experiments were done in vivo on my body.

Please refer to this spreadsheet for the experiment methods. Please refer to molecule syncopation, FAQ, 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)


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


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


Points of interest:


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


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.


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


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


Cells have already reset

Monday, April 1st 2019 Morning (Before)


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


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


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)


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


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


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

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


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)


Most recent visualization.

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


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:

Continuing results

My cells are changing in size (getting smaller). I see this to be a good indication of potential for enforced change. I am learning ways to guide pressure through the body with a combination of electrical oscillations, magnetic coils, and believe it or not; sound waves. Why is that good? It indicates divisions are happening, and that cells could potentially be reforming within my marrow where blood is formed. There are notable changes in platelet counts which would be hypothesized to coincide with change in bone openings. It may also just be due to the fact that I am using significantly higher frequencies now. There are many things I want to talk about but just can’t yet without the proper results. I don’t plan to post any more updates until I refine my methods.

Two main points. Take note of how controlled my phagocytes have become, and become aware of the uses for this beyond cancer. Especially platelet increase/phagocyte adjustment. Each date is 1 slide/sample. Each slide will have multiple self separated environments as mentioned above.

Monday, April 15th 2019

Tuesday, April 16th 2019

Friday, April 17th 2019

Tuesday, April 21st 2019


From here on you can see things starting to settle out. I had begun to use a better system of influence by this point. Less sporadic changes.

Sunday, April 26th 2019

Wednesday, April 29th 2019

Friday, May 3rd 2019

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Self Programed Apoptosis Through Use Of Magnetic Current & Electricity

Tonight while viewing my blood for the first time since I began these experiments something very informative occurred. Here is my blood almost entirely in apoptosis. As theorized, this was a result of many months of consistent magnetic interference. The fields themselves act as waves; or you could think of two fields as two bubbles/balloons pressing against one another. If you do this long enough and at the right frequency you can ensure the cells conform to what is needed. This is expected to lead to cancer dispersals, polarization techniques and ultimately growth and nervous system aid.

At this stage I will be halting all further experiments to monitor how these changes decay into renormalized systems. As I feel there are significant changes I will begin again to adjust them and see if any body manipulations through the recycling of these cells is possible upon cell death or via pointing to specific locations.

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Creating Pre-Cancerous Skin Lesions, and Dispersal Through Biological Induction

Final Day (January 31st)

January 23rd:

January 21st:

January 19th:

January 18th:

January 14th:


The formation of interference in biological circuit is due to a wart found at the cross point on my foot. This would be from beginning of cancerous formation on the arm to the final day. It took about a month to disperse and was directly correlated to the circuit blockage from the plantar. This began as a result of induction experiments on my body, through which daily excitement on fields were applied, using nothing but kinetic movement and significant time intervals.

There were moments where electricity was generated within my body (felt), not measured. Feel free to try it yourself. Simply applying pressure across two fields on your arm can give you physical sensation. However you choose to act with this information, I expect you will be excluding my own discovery for your own desires, as this has broken down into an all out clusterfuck of scientific ignorance. I have my entire life to continue to prove such things, but I do not believe those dying of cancer right now will feel the same way about your actions.

I will look for a way to recross the circuit and replicate the results without a wart (possible a burn might work). There are still other experiments in effect which must wait. I have increased hip width on accident, my hands and fingers have bulkened, and at times grown in length.

This is a result of ratio balancing, and I am now aware that osteoclasting is easily influenced; especially when there are unbalanced values.

My jaw filled in some locations and there are specific spots and conditions on the body which can be met to point to specific areas. The process can be felt. At times there are clear pains while polarities shift. These changes follow ease points and less restrictive connections. Noticing some gum-lines seemed to be change, which stopped.

Eye vision can be influenced. I still have not come up with a way to get it to stay, but have had days where I didn’t need to wear my glasses at all.

January 12th:

Wart has been overall broken apart, you can clearly see the skin lesion is now dispersing as well. Please note that the skin breakage patterns are exactly the same as that of the wart. Think of this as a + pole, and a – pole.

January 11th:

once I had adequately broken down the wart the lesion on my arm began to break apart too

January 10th:

still there, better pictures to allow you to see what I mean

January 3rd:

first pictures of indicators of crossed circuit. Had been there for over a week, I just hadn’t taken a picture yet.


I would like to mention that it is possible to speed up muscle growth exponentially. I had a dent in my leg (deteriorated tissue) from about 6 years of sitting at a computer desk with one leg crossed under the other; sitting on top of it. I spent a few months stretching and running but could not get the muscle to rework itself back into its original structure. It took me about 2 weeks when I started this to get it into original shape, and it has held its shape. I no longer point to it. I have increased arm strength in a matter of days, and the muscles continue to tone/grow based on what you instruct the rest of the body to do.

It is very easy now to choose which muscle locations to grow, and unnecessary to work out to get it to happen anymore.

The body seems to be growing as a matter of thirds, where you pass a threshold and a cell divides. Compression leads to coaxing this to happen, exciting a face and settling it. This push pulls parts of the cell and enacts an excitement or bond breakage. When you excite and settle you set the need. It is painless when you do it correctly. The main factor is Oxygen and how much conditional metals you have in your body. Syncopation leads to cold sensations. Too much excitement leads to hot, and the wave will re-sync, dropping temperature again. Sounds like global warming doesn’t it?

I no longer have an irritable stomach, and all body functions feel much better than before starting all of this. There are a lot of side effects at first which are similar to high blood pressure (which is what keeps us dividing) but they go away. This is like forcing current through a blocked path until the path is no longer blocked.

DNA is nothing more than magnetic instructions which fold over themselves on their third or fourth ratios. You can see it all over the body when you look for different field types. Especially in the face. This is what allows all of this. It is a crude instruction on the cells functions. This can be improved so much with proper induction techniques and specific items and methods which I choose note to share at this moment. I would have gladly done so if I was not being called crazy, etc. Nobody really deserves this information if they aren’t going to start including others. I’ve given too much proof now and require a life of my own. There are many things which are keeping me trapped from doing what I am meant to do.

This also says a lot for immune systems and compatible partners for birthing/DNA combinations. Along with diabetes and allergies. The bodies atomic waves are consistent, and will stay one way until we instruct them otherwise; because they are a part of a closed system. Just like radiation has an incredibly long decay time, so do processes in the body. This is why tetanus happens. Oxidized blood (iron) enters the system, and then adjusts the entire wave state of the closed circuit (body). If we have a predetermined threshold, (vaccine), we now have less of a change if it does happen, because the wave state was already put into a ratio which allows the item to enter without harming, and the wave balances itself out with no perceivable issue.

I used this to cure my chronic Epididymitis (inflammation). I also found I can bring it back by changing polarity for a long enough time.

Inflammation happens because poles are competing and pulling on each other no different than how cancer can form. This will cure MS, ALS, and fertility issues. It’s already been proven that it will cure cancer, and can absolutely be improved upon. Polarities are what allow impregnation.

I have issues with nerves in the toes of my left foot, and I cannot fold them over. As I complete other experiments on parts of my body, I will find a way to fix that. There are more documentations of growth under “biology”, “cataloging growth using quantum mechanics.

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Intro To Molecular Topology And Calculating The 1/4 Sugar Ratio (DNA)

I have included an in depth explanation within the .py/txt files here:
Py File – Updated 01/24/19
Txt File – Updated 01/24/19

Please see “Glucose” for instruction on calculating DNA entry ratios

'Third Type Vitamins'

'You can find these patterns in things like muscle twitch timings and other natural

#Third Type Vitamins:

Vitamin_D = "C27_H44_O3"
Vitamin_D_3_3 = "C81_H128_O9"

# This Vitamin is created through sunlight excitment (syncopation,subdivision)
# H128 / 4 = 32
# This is the type of wave which excites due to squaring off, 
in that it is not easily rectified

# This is why it works so well with calcium relocation 
(bone excitement, Osteoclasts)
# Osteblast, or bone building through Calcium 
is also due to its ability to create square type waves
# In that it causes excitement which allows attachment and division

'Half Type Vitamins'

#Half Type Vitamins:

Vitamin_C = "C6H2O6"

# This vitamin as a half is C3H1O3
# Or doubled is C12H4O12
# This plays a large role in deoxidizing through push -> pull on HOOH
# It acts as a "lubricant" for virtually all functions which use HO

'Closed/System Required Vitamins'

Vitamin_K1 = "C31_H46_O2"

# As you can see this vitamin is not the most stable.
It is a result of closed systems, and would be if it were:

            #These (K and A) are intermediate type vitamins, which act as carriers 
            #or housing units
            #As a function of waves

'You can then take the electron counts into consideration'

#C31 = 186 + H46 = 232 / 3 = 77.333 (remember how the sun uses this very same ratio?)
# 186 / 3 + H46 / 2 = 54
# 54 / 18 = 3 (Shell 3)
# The distance to Sun ratios use this series as well.
# See
visualizing_whole_to_fractional_ratio_a = 1392000 / 72 * 4 #= 77333.333


Vitamin_K2 = "C31_H64_O2"
Vitamin_K3 = "C11_H8_O2"

# Closer ... but still imbalanced
# This is why the K and A vitamins have sidechain functions.
They are synthesized in the body
# Because they can't exist without other objects. 
If they are doubled, or host other elements
# They become balanced

Vitamin_A = "C20_H30_O"

# Samne thing, different wave


Vitamin_E = "C29_H50_O2"

# This vitamin interacts with Testesterone based systems differently than Estrogen
# There are noted differences through SELECT research, and comparisons vs smoking 
and non smoking environments
# Generally those who smoked (excited the bodies system regularly)
received more benefits
# Free radicals are imbalanced waves, These types of vitamins keep them balanced
# In that they allow movement without deterioration

# Regarding Testosterone vs Estrogen, Vitamin E as a circulatory aid, 
and Breast Cancers:

Testosterone = "C19_H28_02"
Estrogen = "C18_H24_02"

'Vitamin_E has 174 + 50 + 16 = 240 electrons'
#When you divide 240 by 3 you get 80.
#When you divide 240 by 4 you get 60.

'Testosterone has 114 + 28 + 16 = 158 electrons'
#When you divide 158 by 3 you get 52.666.
#When you divide 158 by 4 you get 39.5.

'Estrogen has 108 + 24 + 16 = 148 electrons'
#When you divide 148 by 3 you get 49.333.
#When you divide 148 by 4 you get 37.


# E can sometimes thin blood in males and cause higher risk of stroke. 
# These numbers tell me that
# It is due to closer ratios; in that there is a whole 3 difference for men
# And a whole 6 difference for women
# 3 is more restrictive, leading to higher levels of excitement 
caused by the closed system requirement

# Which leads to easier to excite blood
# Which is caused by half bond coagulation. 
# Too much E has been linked to blood issues in animals
# E can help coagulate, but it isn't building long enough chains 
# so it just bonds blood and then releases
# This prevents K and A from working properly

# You would need to increase K intake for E to be as effective as possible
# These are barrier type vitamins due to the sidechain, 
# where they add to waves to keep them together
# Until something arrives to break the syncopations into two separte bonds
# Might prevent breast issues in women.

# Calcium can concentrate even if not lactating which means more HOOH requirements 
# at these locations
# Calcium syncs with Fe
# E works to ensure these deposits are bonded and released by Vitamin C

# Overall the balance for E tends to be preferential 
towards the base ratio for a female body.


Sugar = "C12_H22_O11"

#That is 72_22_88 electrons. Hydrogen22e is 1/4 of Oxygen88e, 
and Carbon18e is 1/4 of 72
#Carbon72e_ is holding 4 groups of Hydrogen/Oxygen together.

#Carbon_18e + Hydrogen/Oxygen_22e/88e = 1/4 of C72_H22_O11 (electrons)
#This also means that 1/4 of 22/88 is 1/8 of the whole molecule (electrons)

Sugar_e         = "C72_H22_O88"
Sugar_e_integer = 72 / (22/88) or 72 / 4
"therefore ..."
#Sugar = 18 multiplied by 4
#Which is 4/4 or 1/3, 2/3, 3/3, 1 + 1/3
                                  #or subdivide_4_13

'Where (e) is an abbreviation for electron count'

#So this means sugar is an ROS with a 1/4 potential for bonds
#H is only an intermediate, where 22 balance 88 as a matter of 1/4
#With Carbon acting as a cap - The ratio over all is an equal 1/4, 1/4, or 1/2.


#It is my expectation that the role of glucose (Lactose) 
#found in breast milk plays a role in
#The level of protein malfunction which results in negative breast developments 
#at an adult age
#Where the carbohydrates within the milk itself lead to bonds broken
#And the 1/4 sugar function is used far too early on

#Leading to attachments on protein strings ending in HOOH
#This activates a calcium bind, and the bind is not broken without proper chains
#Vitamin E may help to maintain said chains.

DNA has 4 bases:

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