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BACTERVIRA:
CREATOR
OF THE SPECIES
Volume 1
by Chérie Phillips
NovaStoic Priest
Theoretical Philosopher
Copyright © 2010-1997
Chérie Phillips.
All Rights Reserved.
Universal Copyright Convention.
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Selected Excerpts from the book.
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New: 2024 Brief.
Copyright © 2024
Chérie Phillips.
All Rights Reserved.
Universal Copyright Convention.
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Chapter 8
BACTERVIRA
STRUGGLE
FOR
SURVIVAL
While we struggle for survival of our own species, the BacterVira struggle for survival of life itself. Their species is the circle upon which all other species blossom.
If the BacterVira are truly the most intelligent species as defined by survivability, you would expect them to have developed a highly ingenious method of survival that far surpasses all other species. I present the physical evidence.
The strategy of the "colony" BacterVira that created the multicellular species is quite possibly the most brilliant survival plan of all time.
While the single BacterVira must individually defend themselves against predators, the colony BacterVira have two symbiotic species fighting the BacterVira predators from two different dimensions!
We not only take care of ourselves by fighting "our" predators which are other multicellular species, but we also take care of the BacterVira's predators such as the bacteria and viruses. Thus, the BacterVira have "two species" together fighting against "their" predators. We have to because if they die, we die. It is an ingenious survival plan that further demonstrates the extraordinary intelligence of the BacterVira.
In the BacterVira, genes are the physical storage units of functions. Each gene contains software of a function (genetic code) with one begin codon and three end codons. They are stored on nucleotides which in the DNA consist of: adenine (A), thymine (T), guanine (G), and cytosine (C), and they are paired as A-T, C-G, or A-U.
The gene software is believed to be in triplet sets of nucleotide codons, which means that the data stored in the DNA of one BacterVira would be equivalent to one thousand 500-page books.
However, I propose that the software data is phonetic/numeric and is coded in "soundwave and lightwave frequencies." Each phonetic alpha is a specific soundwave frequency, and each number is the color of a specific lightwave frequency. Thus, the genetic software is written in patterns of musical color.
The color and sound of a "set" of nucleotides is the codon that determines the gene function. By varying their light frequencies and sound vibrations, gene functions can be changed.
A set of triplet nucleotides could be coded with many different frequencies of lightwaves or soundwaves, and, thus, a set of similar nucleotides could store many different functions. Also, dissimilar nucleotides could store the same information if their set of lightwaves and soundwaves have the same values.
Messenger RNA retrieve the gene function stored on the DNA. The messenger RNA delivers the codons to the ribosomes located in the cytoplasm, where the BacterVira reads the codons for specifications from which it engineers the amino acids into the specified chemical configuration of a polypeptide chain.
BacterVira can make "new" functions by changing the codes of the genes, and the Reptilian part of the brain can make "new" functions of the Self by communicating data from the environment.
In the creation and evomorph of the species, the BacterVira determine which gene codons to contribute for: (1) structure - genotype, and (2) characteristics - phenotype: tall, short, red, green, curly, etc.
Natural Selection functions by contributing to the phenotypes. The phenotypes are their stimuli determined from feedback we give them from our environment and stored on our memes. The BacterVira "read" the meme codes and translate them into gene codes at night while we sleep when they also clean up and re-energize the BacterVira neurons.
If we cut out a gene, the codon could relocate to another gene. Thus, the true way to alter a gene function is through functioning of the Self during interaction with the environment.
While genes are the coded brains of the individual worker BacterVira; they are also their replication units. The brain of a complex organism is a colony of BacterVira neurons. The genes function as the brain of the individual BacterVira neuron while the BacterVira neurons function as the brain of the multicellular structure.
Because the BacterVira are cloned, with few exceptions, they have individual gene brain function, as well as collective gene brain function.
Sperm are highly evomorphed viruses with protozoa cilia, and must enter the highly evomorphed bacteria, the egg, in order to reproduce the species of animals. The sperm and egg were specifically created by the BacterVira by evomorphing the functions of three organisms, viruses, protozoa, and bacteria to function for the purpose of reproduction.
A male fetus cannot be transformed into a femelle fetus. However, a femelle fetus could be transformed into a male with hormones in the developing fetus. The transformation process is unidirectional and can only go from femelle to male and not vice versa. In fact, that is how the male is formed, by first being a femelle and then transforming into a male in the fetus. Thus, the femelle form is the default form of all fetal animals.
If femelles became extinct, males could not carry and give birth to a fetus. The function of reproduction is unidirectional. A femelle can give birth without a male, but a male needs a femelle womb and including a femelle brain, to reproduce.
Nor can a fetus develop normally outside in an artificial womb. The reason is that the femelle brain has the exclusive ability to transfer maternal memories of the species to the fetal brain, and, if this does not occur, the fetus will suffer brain damage.
The femelle, however, can reproduce without a male structure because sperm is DNA which is available in every cell and can be cloned. In a genetic perspective, the purpose of the male is for protection of the femelle whose exclusive ability to reproduce is unidirectional.
Reproduction is unidirectional because the sperm are actually highly evomorphed viruses. In the microscopic 3rd Dimension viruses have no ability to reproduce independently. However, eggs which are highly evomorphed bacteria, can reproduce independently. This concept from the social order of the 3rd Dimension is mirrored in the 4-D multicellular being.
Both the sperm viruses and the egg bacteria were created by both the Self memes through Natural Selection, and BacterVira genes in response to data transmitted from the memes. The genes function to store genetic material that will return the BacterVira and Self, back to life in successively higher evomorphed levels with each new generation and finally resulting in a new creation when a new survival tactic is discovered.
Together the sperm viruses and egg bacteria join in reproduction to form BacterVira, the most highly evomorphed species which takes the form of the brainstem BacterVira.
The BacterVira are clones, and do not have the distinction of being male nor femelle. However, in our species, they created males from femelles using hormones. Specifically males are created from TDF (Testis Determining Factor) that is on the Y chromosomal gene-brain of the BacterVira. Femelles are an older structure that evomorphed into hermaphrodites until the TDF gene perfected a separate male. The BacterVira created males as a survival function to protect the long nine month neonatal growth period when the femelle and the new life are vulnerable to predators.
REGENERATION
The colony BacterVira are extraordinarily small relative to the size of their intelligence, which functions in their social colonies in a network, but also individually, such as the immune BacterVira. Yet, the colony BacterVira cannot function in isolation, but must function within their social colonies to survive and express their highest intelligence.
The BacterVira show diverse intelligence far beyond our capabilities. In the liver, the hepatocyte BacterVira live only 3 to 500 days, but are quickly replaced using mitotic division. In four months, the hepatocyte BacterVira can regenerate 3/4 of the liver, and they know precisely when to turn off this abnormal cell division. [17]
It may be speculated that cancer in various diseased parts of the body is caused by the dying BacterVira's desperate attempt to heal itself with regeneration for which the genes in that particular organ have not the capability to be turned off in order to control the regeneration process. The same genes do not work in each organ. It is like hitting a function key out of habit in the wrong program which causes the program to start copying data in a loop; and then you try to turn off the computer, but it will not turn off.
Thus, the key to curing cancer may very well be in studying the intelligence of the hepatocyte BacterVira to determine which gene they turn on to achieve regeneration, and which gene they turn "off" to stop the cell division; and, then clone and transplant the "off" gene into the cancer cell and turn the abnormal cell division off.
The BacterVira function with mathematical precision, and, thus, to fix the machinery of the body requires our understanding the operative mechanics of the BacterVira organ colonies. That is why the BacterVira created the "self" mechanism to function with logic, because the whole organism can correct the problem in a shorter time.
By understanding their intelligence, we can learn from them and enhance our own intelligence. That is how we learned to fly, by imitating the creations of the BacterVira. Who would have thought a large machine could fly in the air if we had not first seen the birds achieve flight?
MITOCHONDRIA & CHLOROPLASTS
The BacterVira also created two important single-celled species: (1) the "chloroplasts," with a separate gene configuration to work for its multicellular plants, and (2) the "mitochondria" with a separate gene configuration to work for its multicellular animals.
The mitochondria and other organelles created by the BacterVira generate in the embryo, and, fascinatingly, are born at the same time as the organism to develop as vital functional parts. There are important reasons for the separate gene structure.
The mitochondria convert ATP into cell usable energy. Now suppose the mitochondria genes were located on the cell chromosome. Then they could not roam about freely to produce greater energy and would be subject to disablement during a viral invasion when the energy of the BacterVira is a matter of life and death.
The chloroplasts function in a similar manner to produce energy for the plant derived from sunlight.
Being bound by the chromosomes would make the task of the mitochondria and chloroplasts more complex, for the higher level of intelligence seeks the route of simplicity over and above complexity. Similarly, when you perform a mathematical operation, the last thing you do is simplify your answer.
Another advantage of locating the energy producing genes within the body of the mitochondria is that only one parent contributes genes to the mitochondria. That is the femelle. This is also a high level survival function, whereby they may thwart the efforts of their most vicious predator, the viruses, and, thus, with less chance of the mitochondria genes being altered significantly through mutations or by Natural Selection that so strongly affect the other genes of the chromosomes.
The different chromosomes while they all look alike, may perform different functions, and may represent gene memories of the past functions
The different brain realms, organs, and cells have access to the nucleic chromosomes that hold the gene functions of the body. The mitochondria genes may have been coded separately to thwart the Reptilian Realm of the brain which through its conniving behavior could shut down the whole body and achieve greater control.
The body may be shut down by activating certain genes on the mitochondria.
Thus, until the genes in the mitochondria are decoded, we do not truly know the functions that the complete chromosomes hold. Further, we must always keep in mind that because the genes are storage units of the chromosomal brains of the BacterVira, they can be changed to hold "different" information. They are not coded permanently, but only consistently out of "habit."
As a survival tactic, it is essential that the mitochondria maintain its master energy codes under lock and key without access to any cell, organ, or brain realm, but only the mitochondria energizers. Thus, it is important to keep the mitochondria codes the same in each successive generation with only slight enhancing variations allowing for production of energy as its sole purpose in life. Thus, having the femelle as the sole contributor of the mitochondria genes allows for stability in this very important energy function.
Thus, the genes of the mitochondria are a part of the chromosomes of the multicellular animal, and were deliberately created for the purpose of producing cellular energy. This concept is important to understand that all genes of the chromosomes are, thus, "not" located on the DNA within each individual cell, but some are freely functioning separately within the cell as mitochondria, and other organelles. The same principle holds for the energy producing chloroplasts in plants.
The theory that the mitochondria just happened to be engulfed and developed a symbiotic relationship with the cells denies the highly evomorphed intelligence of the BacterVira. Cannot a creature that creates all the species of multicellular plants and animals in the world also create a simple mitochondria to produce energy? How much more intelligence would that require?
But how would the BacterVira have had any energy before it created the mitochondria? Bacteria and viruses do not have mitochondria. Yet they manage to get where they are going although it would be both inadequate and too complex to produce energy to support, for instance several tons of dinosaur. Once the bacter and vira evomorphed into BacterVira and began creating multicellular creatures, then it was also necessary to create the mitochondria to provide sufficient energy.
Although we may sometimes feel low on energy, if we had no mitochondria, we would be unable to carry on even simple day to day living processes. They are so vital to a multicellular creature that their genes were placed in a separate body within each BacterVira as a preservation and protective measure.
Also, by having the genes separate from the chromosomes, the BacterVira has the opportunity to correct energy problems without even having to decipher the nucleus chromosome genetic codes. There is a connection between energy and life - with energy, you have life; without energy you have no life. That is how important energy is that it came wrapped in its own special packaging.
VIRUSES
Viruses and their counterparts, viroids, prions, and virons evomorphed from the primordial non-living Vira that entered the non-living Bacter and became the BacterVira.
Under the BacterVira Theory, light waves represent the mathematical structure of light before entering the BacterVira and transforming into discrete quantum particles of consciousness. The mathematics of quantum mechanics proves that viruses are actually "living," but are just "weak" particles of consciousness, and, thus, should also be formally classified.
Most viruses are renegade genes that were once part of the gene codes. Thousands of BacterVira workers die every minute, as their lifespan is relatively short, and when they become weak or worn-out, they are subject to replacement in a process called apoptosis or necrosis. Consequently, expounding their unwillingness to die, several genes survive as viruses or their counterpart -- prions, virons, or viroids, but their genes, having been displaced, no longer are able to configure as before, and, thus, take on their own non-living existence that is drawn back to the living cell to live once again.
Also, some animal genes can survive consumption as food and become viruses or their counterparts. Viruses can also enter a structure from other organisms or sources such as from laboratories, from needles, from blood transfusions, other's sneezing on you, and so forth.
We should focus our research on developing some cloned trojan BacterVira to attract them, but that pass through the digestive system, and once they come out, destroy them with certain frequency of light waves that will return them to dust. We should not use the method of just blocking their entrance into the cell because they can overcome this quite easily by reconfiguring. Or, they just go to the next person. They must be destroyed by certain light frequencies after removing them from the body.
Thus, viruses form their own identities as disease organisms which then replicate within the worker BacterVira of the host. The worker BacterVira recognize them as their own genes because they once were, and welcome them. Apparently, there is some kind of identifier that the genes all have. After entering the worker BacterVira, the viruses modify the existing gene codes. The genes of the viruses then begin to function for replication of themselves rather than life structure support of the worker BacterVira, and, thus, cause chaotic functioning. A virus functions with the mission to replicate at any cost, even at the death of its host.
The symptoms of our illness are actually the illness of the microscopic BacterVira who live in another dimension different from ours. That is why we can do little more than wait for their battle to end. We help them by shutting down most of the system of the whole Self. When we take drugs to suppress the symptoms so that we can keep working, we are diverting precious energy that they need to deal with the invasion.
The battle against the viruses and bacteria takes place in another dimension, the 3rd dimension. So if we close down the 4th dimension of our world, that gives them concentrated energy to protect the colony from this invasion. Actually, the outside bacteria and viruses are attempting to mate with the cloned BacterVira, and which destroys their purity and causes mutations, some of which are destructive.
Because the worker BacterVira gene brains are exact replicas of each other, when a virus enters a worker BacterVira brain and takes over and changes its configuration, its altered function begins to spread, and chaos ensues because the BacterVira neurons can no longer function in harmony. However, the BacterVira has a few vital worker BacterVira with different gene configuration to assure that the individual does not completely shut down. That is why the BacterVira created a different genetic code for Mitochondria, and only allow their codes to be transmitted by maternal genes to further assure they are unaltered.
With the invasion of the replicating virus into thousands of BacterVira, how could it not cause behavioral changes in properties governing the Self mechanism. A virus is both a coded memory brain and a reproductive organ. A high level functioning virus could replicate without setting off the immune system by entering the BacterVira neurons themselves. This would involve permanent behavioral changes in the organism resulting in functioning disorders. Some types of viruses, such as viroids, prions, virons and others, which are incredibly small and virtually undetectable without sophisticated technological diagnoses could also cause behavioral disorders.
Autoimmune diseases may be such viruses, viroids or prions which are too small to be detected with present day technology; the cells of the organism's immune system are invaded, reprogrammed, and begin to attack its own progeny.
The purity of the cloned BacterVira is a survival tactic also which assures that the whole Self can exist. The BacterVira clones function with mathematical precision and are able to create and evomorph only because of the virtual purity of their memory. However, it is important to understand that the cloned purity of the BacterVira only works at the microscopic 3rd Dimension. When we try to apply their social order to our 4th Dimensional world, the result is much pain and suffering.
It is conceivable that a high level virus which alters the genes, could also cause an enhancement in functioning of the organism if perchance the alteration functions harmoniously.
Further, it is possible that some viruses may be gene survivors of dead life structures which were in the inorganic state but live again once entering the cell of a life structure.
Thus, the cure for the common cold is to help them battle the invasion by understanding what they need to defend themselves. Rather than focusing on what we can do to defend ourselves, we need to focus on what we can do to help "them" defend themselves, specifically, their genes-brains. We need to think in terms of 3-dimensional solutions instead of 4-dimensional solutions.
IMMORTAL GENES
The BacterVira do not have "time" in their 3-dimensional universe because "light" is the "time" that structures "space" into "spacetime," and the particles of light are too large to radiate light in their dimension. So they live in perpetual darkness. There is no need for eyes when they have no light. Thus, they used mathematics as their "vision," in order to create our structures in the 4-dimensional universe of spacetime. That is how they acquired their incredible mathematical knowledge.
Further, they created the heart to create time. Without the heart, they would not know how much time we can exist in our world. They heart not only serves as a pump, but it is a clock. They also have encoded the genes with a time end code called the telomere that is the natural end of the chromosome.
Thus, the heart and telomere serve as a clock to the BacterVira because "time" (light) does not exist in their 3-dimensional world.
Their multicellular creations allow them to exist simultaneously in the 3rd and 4th dimension.
It is possible that life did not exist in their dimension and it was not until they entered into the 4th dimension that they became alive by processing the L-Force light energy.
Nevertheless, the BacterVira may preserve the memory of the Circle of Life in suspended animation after the life structure has deceased, in their dimension as non-living structures, and in our dimension perhaps in bones. Or the body may go to "seed," decomposing into gene seeds in the dried state, just like plants do when they end their structural existence. Or, the decomposing bacteria themselves may function as preservation structures. Perhaps they store some vital genetic memory on molecules that lie dormant in the dirt. The extraordinary intelligence of the BacterVira has shown relentless and consistent diversity as the most potent survival tool of all living things.
We may also expect to find some type of gene memory, other than accidental amber, in the dried state and preserved in such a manner that it could restart evomorph with complex modification from the reset point; the most simple gene structure which could perform this feat is the virus which can exist in both the non-living and living state. Also, certain kinds of bacteria are capable of existing for a very long time in the non-living dormant state, such as the tardigrade.
And then there are the molecules themselves which can be encoded to restart evomorph under certain conditions.
The BacterVira have created both the life and non-life structures to assure it survives any catastrophic event and is brought back to life. It would be fascinating to do more research on the recycling processes of life structures because there may be more going on after death regarding gene preservation and our own immortality than we presently realize.
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