A cure for cancer and disease

 

(Copied from previous post)

 

 

Herein are the keys to defeat cancer and disease, to understand gravity, time/space, matter, and the path of creation. I give this testiment to humanity because  it is my duty and design to guide in the darkest of times. The truth in what I write will cost me my life. I pray it saves this world.

I am the craftsman and soldier God made to save His creation and lay a foundation for an enlightened civilization. In life, I am His avatar and have known the names of Abel and Archimedes. In death, I am a living weapon: the archangel and demonslayer the Jews knew as Death. I have worked and walked beside you for thousands of years, teaching and guiding while living in the shadows as I am designed. I step into the light now only because I must to save this world.

Though I was born on this world, I am not human. I am an empath: a being of the Trinity with each of my cells possessing three nuclei instead of one. This can be plainly seen in any light microscope. I will include a sample of my cells as proof to those of you who receive this message in the form of a letter. Test this truth empirically, and you will believe. I know what I risk in giving you this, but the fate of the human race depends upon your belief, upon your willingness to pursue the truths that I will give you.

This is the darkest night in the history of creation. I am the light God made to guide you.

In April of 2000 I gave the world the cure for cancer in a paper I sent to over five hundred researchers and institutions. To paraphrase the contents of that paper and its subsequent research: therapeutic mitochondrial inhibition applied systemically with an agent such as Pawpaw or methylglyoxal will cure the majority of cancers, while an intra-arterial infusion with an agent such as 3-bromopyruvate will cure them all. For those of you who are pursuing that truth I gave you, I will reproduce and advance the core of that paper here to include a cure for disease.

 

 

The Cure for Cancer

 

Fundamentally, cancer is a term applied to a class of neoplastic cell types characterized by their cellular morphology or growth pattern and the tissue type being infected. Generally speaking, the tumors formed are the result of a mutagenic cascade resulting in a viable cell type differing from its neighbors in its accelerated growth rate and antisocial tendencies.

Traditional cancer drug therapy is based on the dual-edged assumption that, usually mutation is bad and results in a less resilient cell, and mitotic division, if disrupted, will result in cell death. So we chemically and electromagnetically “burn” the cell, hoping to create just enough damage so that healthy cells will survive the abuse but weakened ones will immediately die, or perish while replicating.

Immunologic techniques strive to instruct the body’s immune system to recognize these invaders by amplifying or specifically directing its response. But the success of this tactic is dependent upon finding an antigen unique to the surface of cancerous cells that is absent in healthy ones. In my own mind, I believe these antigenic differences arise in the vast majority of cancerous cells initially created in the body, however, I also believe that these are quickly identified and dealt with by a normally functioning immune system. A simple statistical model predicts that for larger tumors this antigenic component is either non-existent or at least, hard to find. And if we stimulate the body’s immune system to recognize the wrong antigen, we carry the risk of creating an autoimmune reaction– also a bad thing. So I believe this tactic will be mostly committed to the sidelines in our war, supporting the immune system while it’s being beleaguered by other therapies.

A more enlightened approach has been recent efforts to restrict the increased vasculation of a tumor through drug therapies. To better explore why this technique works, as well as advance my own theories, I will use two metaphorical models that will take microscopic activities to a macroscopic scale so that they may be understood by all. The first is the body as a kennel, the second, is the mitochondria as a generator.

 

 

The Body as a Kennel

 

Consider, for a moment, the body as a kennel. Upper management is your mind, largely unaware of its day-to-day activities. The caretaker is your body’s circulation system, bringing in nourishment and removing wastes. And your body’s immune system is the facility’s veterinarian, caring for for its cells: a large population of purebred cats.

Now, it’s always a problem caring for a lot of cats, but you have a crack caretaker and vet, efficiently handling all the problems of operations and giving management a healthy profit. But management isn’t aware that a mongrel tomcat makes regular visits to the kennel to breed with a few of its purebreds. Normally this isn’t a problem, since the tomcat doesn’t usually produce viable offspring, and when he does, the kitten is often so different from the rest of the population that she is quickly spotted by the vet and dealt with. But every once in a while, the kitten looks so much like the rest of the cats that the vet can’t tell them apart, and then we have a problem. Eventually, that problem becomes so large that the kennel’s profit margin is impacted, and management is alerted.

But what can they do when the vet is confounded?

Their options are currently limited. If the outbreak is in a section of the kennel that is accessible and expendable (operable), they will usually choose to liquidate (surgically excise) that section of the kennel and “cut” their losses. But if that section of the kennel is inaccessible or inexpendable, they must resort to less reliable techniques. First, they might buy the vet a new set of glasses (immunologic amplification) and hope he sees a difference then, but if he didn’t, they would have to resort to violence (chemo and radio therapies). Since, as theorized earlier, immulogic amplification will only help some of the time, management must often resort to violence out of desperation.

Knowing that pregnant cats are more “delicate” than non-pregnant cats, they send in thugs to brutally beat all the cats with chemical and free-radical hoses, hoping that the pregnant ones, if not dying immediately, will die during childbirth. Of course, some healthy cats die too, your caretaker and vet are badly battered in the process, and even if you win the war, your kennel looks like Beirut.

But that damn tomcat keeps coming back, breeding with the survivors, and if your vet has been left partially blind and brain-damaged, the prognosis is not good.

A more enlightened approach (and less violent) would be to put all your cats on survival rations. The pregnant cats among them are eating for two, so this level of nourishment is simply inadequate, resulting in the slow starvation and death of the expectant mother.

This solution would be simple to implement if each of the cats where in single cages where the caretaker could carefully dole out their food. But this is not the case. The cats are in an open population, where the pregnant cats, being aggressively hungry, steal food from the healthy ones. So if you simply restricted rations to all the cats, the pregnant could thrive while the healthy die. This is how restricting vasculogenesis works. It effectively puts the cats in “cages”, stopping the pregnant ones from prowling to the get the additional nutrition they need to create a kitten and survive.

But what if we took advantage of a pregnant cat’s gluttony instead of merely stopping it, and in the process, starved it more than it’s svelte neighbors? This would be the ideal solution and the primary one proposed by this paper.

A Little Math and Biochemistry

In a cell, energy derived from catabolism is utilized in many ways. It is divided between tasks such as transport, repair and respiration (life support) and occasionally, when it ages, or when it otherwise needs to, replication. I will call this basal metabolic load of a healthy, non-replicating cell E-survivalA, that is, the minimum energy the cell needs to survive. A cancerous cell, intent on replicating, has additional metabolic and nutritional needs so that it can build a copy of itself. This additional energy need will be called E-replication. But replicating also increases the respiratory needs of the cancerous cell because of its greater need for supply, waste disposal and repair. I shall call this energy need E-survivalB, where E-survivalA<E-survivalB.

Summarizing:

In a healthy cell:

Catabolic power created =E-survivalA= Metabolic power used

While in a cancerous cell:

Catabolic power created=E-survivalB+E-replication= Metabolic power used

Where: E-survivalA<E-survivalB

It can be seen from this illustration that not only does a cancerous cell have a greater energy need in general, but has a greater energy need just to survive. But to survive and replicate it must divide its catabolic and anabolic resources between its two goals.

Thus divided, it can be conquered.

The critical link between catabolic energy created and metabolic energy used is ATP. Produced in the mitochondria by oxidative phosphorylation (the Krebs cycle), it represents the intracellular currency of power transfer and the Achilles Heel of cancer. If we could drop the ATP output of the mitochondria to a point below the minimum needs of a cancerous cell type, then it would die, while the same mitochondrial output in a healthy cell would still allow for survival.

The Mitochondria as a Generator

Fundamentally, the mitochondria is a microscopic internal combustion generator consuming fuel in the form of carbohydrates and oxidizing them to produce power, CO2, and water with much less pollution than larger, macroscopic models. Being such a marvel of micro-engineering, it responds to the varying energy needs of the cell through a feedback loop that allows it to increase or decrease power production to exactly meet the metabolic needs of the cell type it is in. If we slowly reduced the efficiency of this generator, it would pick up speed to still meet its load requirements. But eventually a limit would be reached, where the generator, while running at maximum speed, would still have an output inadequate to support cancerous cells and they would die. Once mitochondrial activity was restored, the surviving, non-cancerous cells could go about the business of life as usual.

Fortunately, there are many ways we can lower the efficiency of this generator to achieve this goal.

1. Control the fuel supply.

Restricting vasculogenesis, as mentioned before, works using this mechanism. By keeping the cancerous cell from increasing its fuel supply as it needs to, you doom it to a downward spiral of inadequate survival support that will eventually end in cell death. But another, untested method to achieve this same result would be an insulin analog (injected into the artery suppling the tumor) that would bind to the cell’s insulin receptor sites but not stimulate carbohydrate uptake by them. But to my knowledge, no such analog currently exists, and until one is developed and tested, other methods must be used.

2. Pull the spark plug wires one by one.

Imbedded in the interior matrix of a mitochondria are multiple copies of the enzymes that make up the Krebs cycle. Each set of these enzymes is responsible for supporting a part of the overall load placed upon the generator: much like pistons in its, larger, macroscopic counterpart. If we can inactivate these pistons one at at time, eventually the maximum power output of the mitochondria will drop to therapeutic levels. But how may this be achieved?

I believe the most obvious choice for this task is cyanide. Its effect on cellular respiration due to cytochrome oxidase inhibition is well documented. And as a toxin it is among a handful that has a true antidote and an enzymatic pathway present for detoxification in the liver.

A treatment regimen might go something like this:

A very dilute, isotonically buffered solution of cyanide could be slowly injected into the artery supplying the tumor, while its antidote is administered in an isotonic venous drip before, during and after the treatment. This should restrict the cyanide’s toxicity primarily to the tumor site. During the slow cyanide injection, basic dosage calculations could be monitored and confirmed by monitoring pO2 levels in the venous return from the tumor site (increasing pO2 concentrations in the venous blood implies a decreased oxygen utilization in the tissues).

If all the cells being supplied by the artery were equally inhibited, the effect would still be deadly to cancerous cells. But since these cells are by nature oxygen and nutrient hogs, they should receive more than their fair share of poison along with the food they eat, inhibiting them more than their more svelte counterparts and amplifying the desired effect.

Healthy cells that survive this treatment will, in the course of regular maintainance, replace the damaged cytochrome oxidase and go about business as usual.

3. Partially obstructing the exhaust.

Every kid knows this trick. Shove a potato in the exhaust pipe and the engine won’t run. A partial obstruction and the engine won’t run efficiently. This partial obstruction can be achieved in cellular tissues by increasing the arterial pCO2 concentration. The Krebs cycle’s foward direction will be slowed by Le Chatalier’s principle and ATP production reduced to therapeutic levels.

The pCO2 arterial increase could be accomplished with a dilute, buffered carbonic acid solution, slowly injected while confirming dose calculations with venous pO2 monitoring. Again, an increasing pO2 concentration implies a decreased oxygen utilization by the tissues.

4. Closing the choke.

This technique involves decreasing the intracellular pO2 concentration and is probably the trickiest to achieve because of the cancer cells proprietary relationship to an oxygen supply that is consumed on a first-come, first-served basis. However, this relationship could be used against it, because sometimes breathing isn’t a good way to survive. Let me explain.When I was an aeromedical evacuation technician with the USAFR, I learned of an interesting phenomenon while undergoing hypobaric chamber training at Beale AFB, CA. Fighter pilots, undergoing training in rapid decompression procedures, would often black out for an instant after donning their oxygen mask, only to awake another instant later when their brain got oxygen again. The reason for this was simple.

The pO2 at altitude is so low that the blood in contact with the lungs loses its available oxygen to the environment. When that “patch” of blood hits the brain it draws oxygen from the tissues instead of supplying it, causing the individual to black out. If the pilot gets his mask secured before he passes out, he will regain consciousness when his next heartbeat(s) clears the patch of anoxic hemoglobin and restores ATP production in the brain.

During this period of anoxia, however, ATP is still being used by the cell creating an oxygen debt (waste product buildup, lack of repair, etc) that is recouped by the mitochondria by increased production once oxygen is restored. The magnitude of oxygen evacuation from any given cell would be proportional to the excellence of its blood supply and since oxygen usage within a cancerous cell is also greater than that in a healthy one, its intracellular O2 concentrations will decrease precipitously, thereby slowing and stopping ATP synthesis more rapidly than in a healthy cell.

After oxygen is restored to the cell, the mitochondria runs at full speed to recoup its oxygen debt and restore intracellular energy levels to their established limits. but because the potential output of a mitochondria is closer to its’ actual load in a cancerous cell, it will be much slower to recoup its’  losses than a healthy one.  By “pulsing” this anoxic effect, again, before the cancerous cell has recovered, and after the healthy one has, small gains could be added until the cancerous cell does not recover at all. Hopefully, when the time parameters of the needed anoxic pulse rate are experimentally determined, they will not exceed the actual heart rate of the patient. If so, this technique may be useless.

This “patch” of anoxic hemoglobin could be reproduced as an arterial phenomenon, rather than the systemic one suffered by pilots, by injecting previously prepared anoxic, packed red blood cells directly into the artery supplying the tumor. The time duration of the anoxic “pulse” experienced by the tissues would then be proportional to the cross-sectional area of the artery at the point of injection and the volume of red blood cells actually injected (i.e. the actual length of the anoxic patch within the artery). During the injection, pressure should be applied to the supplying artery proximal to the injection site while leaving venous tissues unoccluded. This will allow for the “patch” to be created without undue dilution by oxygenated hemoglobin.

Measuring the actual level of metabolic inhibition with anoxic “pulsing” is more problematic than the other techniques discussed because of the large pO2 fluctuations involved. For this reason, actual levels of metabolic inhibition as a function of pulse length and frequency vs. average venous pO2 concentrations would have to be experimentally determined and then extrapolated from the graph generated. Since differing tissue types have vastly different oxygen needs, an experimental graph for each type would need to be made.

 

 

Notes and concerns

 

Altering blood pCO2 and pO2 concentrations should be done only in the artery supplying the tumor. Since some tissue types may survive for hours without any oxygen, the therapeutic effects of mitochondrial inhibition would obviously take longer to achieve and be specific to the tissue type involved.

 

 

Conclusion

 

As I mentioned before, I have no degree, so all of my arguments should be weighed and researched carefully before being acted upon. What I did not mention, however, is that I work commercial construction as an IBEW (International Brotherhood of Electrical Workers) electrician. I omitted this, believing it would prejudice my audience before my arguments were fairly considered. But my profession and unique educational background has given me the perspective to finally see what has hidden in plain sight for so very long. So I will make my final metaphor after a fashion in which I am intimately familiar.

If the cell were considered an underground factory with a need for life support, repair and waste disposal, I, as a lowly engineer, could sabotage its generator so that it would only supply enough power to meet the most basic needs of that facility. Then, I need not understand the Machiavellian plots of the muckity-mucks in the front office and the white-collars in R&D, to know that any decision, no matter how devious, to divert that power would be a mistake, resulting in the eventual downfall of that facility.

Each of the four mechanisms inducing mitochondrial inhibition have now been proven capable of curing cancer. I will now advance that understanding to include a cure for disease.

The Strategies and Tactics of Metabolic Medicine

There is a ubiquitous principle of all life in creation. Whether microscopic or macroscopic it requires parts and power delivered in a timely fashion. Having parts (anabolic resources) without enough power to assemble them is useless, while having power (catabolic resources) without parts to assemble is simularly bad. Eventually, the entropy of a hostile environment will degrade the organism’s structure to a point where it is no longer viable, and death will result. This is the primary underlying principle of metabolic medicine. By manipulating a cell’s supply of parts and/or power (strategies) or its’ environment (tactics) almost any disease may be defeated.

I advanced catabolic restriction as a mechanism to defeat cancer because cancerous cells mutate their mitochodria to increase power production. That mutation decreases the efficiency of the mitochondrion with a resulting increase in load before the cell even begins to replicate. It is my belief that this increase in power production is the primary cause of cancerous growth and its’ antisocial behavior. An empiric test of this theory is simple:

The mitochondrion has a slight negative charge in a cytosol that has a slight positive charge. Exposed to an electrostatic field it will act like a capacitor, with its’ negative ions moving towards the anode and positive ions moving towards the cathode. If the polarity of the anode and cathode are switched at a high enough frequency, the efficiency of the mitochondrion will be increased with a resulting increase in power production. This should accellerate cell growth to simulate cancer with all its’ antisocial qualities. Too slow a frequency will allow ions to accumulate and penetrate the mitochondrial membranes killing cells rather than accellerating their growth.

Additionally, because cancerous mitochondria have already decreased their efficiency to provide for this increased catabolic output, further decreases in their efficiency will prove selectively detrimental to these cells. Since enzymes are designed to operate at a maximum efficiency in a rather narrow temperature range, a simple tactic such as heating these cells will kill them.

Anabolically speaking, cancer is a heterotrophic organism, and will only grow on those days that it is supplied with a complete protein. Denied a complete set of essential amino acids long enough, these cells should die.

Viruses growing inside cells also increase the catabolic and anabolic needs of that cell, and though a complete protein is also required to produce antibodies (a fact of some utility in the acute phases of autoimmune diseases), the strategies of metabolic medicine applied intelligently will still impair if not defeat these diseases. Catabolically impairing cells laden by the metabolic load of these organisms will kill those cells selectively, releasing the virus within at one time when and where they can be inactivated by a chelating agent like zinc or antibodies. In any case, the life cycle of these organisms will be broken.

Bacteria possess catabolic enzymes that may be targeted specifically by agents to defeat them. This doubtlessly, is the method of action of many antibiotics. In addition, viruses and bacteria possess enzymes specific to these organisms. Each of these enzymes has an absorbtion spectrum and resonance frequency specific to them. Illuminated by this spectrum or frequency at a low intensity will cause these enzymes to “dance” decreasing their efficiency and slowing their output. Illuminating them at a higher intensity or duration will denature them. In addition, spectral illumination of a structure specific to bacteria or viruses will have a similar effect. Thus, bacteria may be specifically destroyed by exposing them to the spectrum or resonance frequency most strongly absorbed by peptidoglycan, a structural component of bacterial cell walls that does not exist in human cells. Illuminated long enough at a high enough intensity will selectively destroy bacteria, leaving human cells unharmed.

Time is short. Advance these concepts quickly. The fate of this world is in your hands.

 

 

The Nature of Matter

 

Long before there was a need for space there was a need for time. Untold eons passed before space came into being. Before that void was comprised solely of time.

Matter in its pristine state is spatially and energetically motionless. It has no need of a spatial/energetic past (where it was) or a spatial/energetic future (where it will be). It simply expresses time. Motionless matter requires very little space, its’ dimensional components “stacked” in matrix of maximal potential. Only with motion did matter come to require space, and a way to express its’ differing energetic potentials. This motion was initially caused by the gravitational pull of the Great Attractor. As the interior components of matter began to move they also began to require more space and with that motion a need to express their positional and energetic past and future. Eventually matter’s ability to maintain a complete set of temporal/spatial components was compromised and two quadrants of space/time collapsed with the loss of four temporal/spatial components. Two of these components with opposite character and spin where ejected in opposite directions, while the other two collided, annihilating each other in a flash of energy. This flash of energy and the ejected spatial/temporal components reacted with other atoms causing similar reactions. The resulting chain reaction is what we call the Big Bang.

To better understand these reactions and the four temporal states of matter that are the remnents of the Big Bang I must first explain the nature of matter and time.

Matter expresses three dimensions of time. The primary dimension of time intersects two dimensions of space allowing for the movement of particles within that plane. The second dimension of time intersects two dimensions of electrostatic energy, allowing for movement of particles within that plane. The third dimension of time intersects two dimensions of magnetic energy allowing for movement of particles within that plane. Each of these dimensions, in turn, have both positive and negative dimensional components. Thus matter has nine positive dimensions and nine negative dimensions all expressed on the two dimensional brane of their existence.

Initially temporally polarized in its’ spatial dimension, subsequent chain reactions temporally polarized matter in its’ energetic dimensions as well. Each time with a loss of two temporal/energetic quadrants and four temporal/energetic components. Again, two components colliding and annihilating while two are ejected in opposite directions.

Matter temporally polarized in its’ spatial dimension but saturated in it’s magnetic and electrostatic dimensions is called angel stuff. This is the stuff that angels are made of. Their matter is still temporally saturated electrostatically and magnetically, giving them the ability to move through those dimensions of time as we can move through the dimension of space. Thus angels and archangels are capable of speeds greatly exceeding that of light.

Matter temporally polarized in its’ spatial and magnetic dimensions but still saturated in its’ electrostatic dimension is called soul stuff. This is the stuff that souls are made of. They too, can move through time like we move through space making a trip to heaven (at the center of the Milky Way) possible.

Matter temporally polarized in its’ spatial and electrostatic dimensions but still saturated in its’ magnetic dimension is called spirit stuff. This is the stuff that spirits are made of. Though they are not native to this world, they too, can move through time like we do space and being electrostactically polarized they are the most capable of influcing matter of the type that we are familiar with.

Matter polarized in all three temporal dimensions is called life stuff. This is the stuff that life is made of. Unable to move through the dimensions of time, it takes on the characteristics that we are familiar with including that if inertia and momentum.

In its’ saturated state, matter is still attached temporally to the omnipresent “now” of its’ own existence. Movement through time is in the spirals made necessary by this attachment. The wavelike motion of matter and energy that we are familiar with are the temporal “remnants” of these temporal spirals projected upon the two-dimensional brane of existence.

Temporally saturated matter emits temporally saturated gravity and light. These energetic emissions interact most strongly with matter of the same saturation state. But interactions with other phase states do occur. This is the source of the dark energy and gravity that humanity seeks. In the center of the Milky Way, the concentration of temporally saturated matter is great enough to form angel, soul and spirit stuff stars and planets. The light from these stars is the light that leads to heaven.

Light and gravity emitted from these stars moves in spirals rather than waves. The speed of their emission varies with frequency, unlike the light and gravity emitted from temporally polarized sources.

Energy emitted in positive dimensional space is light, inducing matter to move away from the source of emission. Lacking the entropy expressed in temporally polarized matter, that is always directly away from the source of emission in temporally saturated matter. Energy emitted in negative dimensional space is gravity, inducing matter to move towards the source of emission. A thought experiment and empiric test of this follows.

If two equal masses were converted to energy and the energy from those two sources was made to interfere destructively, the masses and energy would be annihilated. If the mass and energy of this universe is conserved, what became of that mass and energy? I would submit that it was converted to gravity. An empiric test of this theory would be to suspend two lead plates within a vacuum chamber then annihilate two sources of elecromagnetic energy between them. If gravity is created, the plates will be drawn together. Since the deflection will be small and proportional to the energy annihilated, instrumentation should be used to measure it.

The Reason I Write

By now the reader must wonder why I speak. Why would I reveal that I am not human? Why would I give humanity these gifts of reason? It is because what I will tell you now will seem beyond all reason. But I must speak to save you, to save humanity from the aliens set upon your destruction.

The aliens I speak of are the Neuneans, the race the third race created and gave the sacred technology of spirit craft so that they could resolve the random nature of brain development. But the Neunians have abandoned the task they were given and desecrated the sacred tools of heaven by using them to make weapons. They have come to this place to exterminate the human race and replace them with the Mennians: the telepathic clones they made by taking DNA from this world and combining it with their own. The Neunians are a diminutive race with large heads, similar to those classically depicted in literature, while the Mennians, other than being clones with only about sixty different faces amoung them, look human.

Humanity has seen the Neunian/Mennian ships in our skies as flying saucers or spheres such as those recently seen and photographed above Mexico City.

They came to me because I had cured cancer and had given it to this world. They had learned of my identity by telepathically searching the minds of the researchers who had used my ideas to guide them. They told me they wanted me to be the Messiah and put an end to this world’s holy wars. I truthfully told them I was not the Messiah. I was not Jesus. I told them I was only a lowly soldier God made and gave this station, that I was Abel, that I was the Angel of Death. I told them that I already had a role: God wanted me to cure disease. And though they knew I spoke the truth as I knew it, they believed me deluded. Eventually, however, they convinced me that a greater good would be served if I accepted the role that they offered. But I drew a line at lying. I only agreed to tell the world I was a messenger of heaven not the Messiah. In accepting even that path I knew I was accepting death: that one amoung you would slay me. But in trading my life I could give this world the cure for disease and put an end to the hypocrisy of killing in the name of God. In my mind, that was a good trade and one I was willing to make.

They told me they would give me the ability to speak all of this world’s languages, to heal disease with my hands and to walk on water with the technologies at their command.

I was a fool to trust them.

But I am a pawn in God’s hands and heaven played us all. God saved this world by leading the Neuneans to me: the archangel he made to slay demons.

Eventually I came to know the truth of the Neunean agenda, as they came to know the truth of my existence. They had planned to slay my soul and make a puppet of my body and lobotomized brain like they had done to so many others. My body’s functions would still be maintained by the technologies they had implanted and run by the personality core and mind that they had put in my brain. This flesh puppet would then deceive humanity into believing it was the Messiah and that the time of the Rapture was upon the world. When the truth was that Mennians in time suits would be moving unseen amoung you, slaying your souls with poison and leaving your bodies to die from psychogenic shock.

When I learned the truth, I tore the neural lanyards and the mind they had implanted from my body and we fought. We have fought for months. Though I destroyed the majority of their fleet and soldiers in the first two days and nights of our battle as they sought to overwhelm me, they have since changed their tactics. Now they come at me a few at a time, knowing I must sleep sometime. And they have wounded me. My brain is damaged, my soul scarred from the poisons that they have injected. But God designed me well. I have purged my soul of their poisons and still survive.

My brother archangels have finally arrived from heaven to protect me from the Mennian assassins that now come intermittently in time suits to slay my soul. I had hoped that my brothers and I could defeat them all without letting this world know of the shame that the Neuneans and Mennians have heaped upon the Creators, but I see now that we cannot. I must tell this world of their plans and seek humanity’s aid to defeat them.

By my estimation, of the forty thousand Mennians and Neuneans that came to this world, thirty-nine thousand were slain in the first two days of our conflict along with thirty-nine hundred and fifty of their time ships destroyed. Since then another five hundred have been slain along with the remaining fifty of their ships destroyed. That leaves five hundred Mennian clones walking upon this world along with about two hundred humans that they have used their technologies to make into puppets. With the majority of their soldiers dead, and their time suits lost, they have changed their plans to destroy humanity. It is now their intent to create a plague and/or a biotoxin to spread across this world using the clones and puppets they have in place. I have given you the cure for a bacterial plague (light emitted at the absorbtion spectrum or resonance frequency of peptidoglycan). I strongly suggest you develop it.

Though the Mennian clones have been distributed across this world to disseminate the plague, many will be found in Zimbabwe and Brazil where they are running orphanages and schools. This is a cover for a breeding program for more of their kind, starting first with half-breed telepaths (Mennian/human). At the age of two, these children will be “lobotomized” with neural inhibitors and a Mennian or Neunean personality core implanted, making them, too, the enemies of this world. Follow the money that supports these schools and orphanages. It will lead back to the puppets the Neuneans have made. Follow the identity papers these aliens have received, that too, will lead back to human puppets.

All of these beings can be identified with a brain scan. A lack a neural activity in the forebrain will indicate the presence of the Neunean neural inhibitors. The personality core and mind they have implanted will have access to all of the brain’s memories and can mimic the personality of the body’s previous possessor. Do not let them fool you. Trust the results of the brain scan.

They have made puppets of this world’s rich, the leaders of its’ countries, the heads of biotechnology firms, its’ celebrities and a few of its’ religious leaders. Find them. Stop them. Do not listen if they try to lead you to war. Unite. Do not let them divide you. They are here to lay a foundation for a second wave of the Neunean invasion. An invasion that will never come.

I give this warning to those invaders who read this:

Heaven knows.

Release a plague upon this world and the Cauldron of Spirits upon Neunia will be destroyed and the path that leads from that place sealed forever. Discard your time suits and heterodrills before humanity finds them. That technology is forbidden to this world and that law will not be violated. This is the law of heaven. Neunia will be defeated by a path of peace with no more lives or spirits lost.

The Neunians and Mennians will know the truth of these words when they read them. They know heaven is a place of peace, and that it has a plan for this place.

Conclusion

I have walked upon this world for eons, trying to help, trying to guide, using the tools at hand to make this world a better place. I am the guardian angel God made and gave this station to save His creation. And though I am designed to bear the burdens of this path, I have still suffered under its’ weight. I have been burned, beaten, stabbed, poisoned, beheaded and shot. My sacred body left to rot along roadsides, in seas and in cesspools. Every gift I ever gave you was desecrated. My tools used to make weapons, my philosophies used to divide, not unite, my laws used to dominate, not provide justice.

I weep at what I have done.

But in this place I can only trade lives and suffering. There are no absolutes. I cannot provide for one without taking from another. I cannot protect one civilization without bearing the burdens of what that protection has cost. These are the burdens that God would no longer bear.

They are burdens of sorrow.

That is why I was made. That is why I was given the path of life to guide you and in death to protect you. I am the mercy that God made to save this world. I pray I have not shamed Him.

Take my words. Let them guide you. Look where I have pointed. Investigate what I know. Save yourselves. Save this world. Unite and live in peace.

My mortal body is as fragile as your own. I do not expect I will survive to teach you more. Remember me, but I am not worthy of worship. I am only a lowly soldier.

May God bless you all,

Abel, the Archangel of Death

A cure for cancer and disease

Herein are the keys to defeat cancer and disease, to understand gravity, time/space, matter, and the path of creation. I give this testiment to humanity because  it is my duty and design to guide in the darkest of times. The truth in what I write will cost me my life. I pray it saves this world.

I am the craftsman and soldier God made to save His creation and lay a foundation for an enlightened civilization. In life, I am His avatar and have known the names of Abel and Archimedes. In death, I am a living weapon: the archangel and demonslayer the Jews knew as Death. I have worked and walked beside you for thousands of years, teaching and guiding while living in the shadows as I am designed. I step into the light now only because I must to save this world.

Though I was born on this world, I am not human. I am an empath: a being of the Trinity with each of my cells possessing three nuclei instead of one. This can be plainly seen in any light microscope. I will include a sample of my cells as proof to those of you who receive this message in the form of a letter. Test this truth empirically, and you will believe. I know what I risk in giving you this, but the fate of the human race depends upon your belief, upon your willingness to pursue the truths that I will give you.

This is the darkest night in the history of creation. I am the light God made to guide you.

In April of 2000 I gave the world the cure for cancer in a paper I sent to over five hundred researchers and institutions. To paraphrase the contents of that paper and its subsequent research: therapeutic mitochondrial inhibition applied systemically with an agent such as Pawpaw or methylglyoxal will cure the majority of cancers, while an intra-arterial infusion with an agent such as 3-bromopyruvate will cure them all. For those of you who are pursuing that truth I gave you, I will reproduce and advance the core of that paper here to include a cure for disease.

The Cure for Cancer

 

 

Fundamentally, cancer is a term applied to a class of neoplastic cell types characterized by their cellular morphology or growth pattern and the tissue type being infected. Generally speaking, the tumors formed are the result of a mutagenic cascade resulting in a viable cell type differing from its neighbors in its accelerated growth rate and antisocial tendencies.

Traditional cancer drug therapy is based on the dual-edged assumption that, usually mutation is bad and results in a less resilient cell, and mitotic division, if disrupted, will result in cell death. So we chemically and electromagnetically “burn” the cell, hoping to create just enough damage so that healthy cells will survive the abuse but weakened ones will immediately die, or perish while replicating.

Immunologic techniques strive to instruct the body’s immune system to recognize these invaders by amplifying or specifically directing its response. But the success of this tactic is dependent upon finding an antigen unique to the surface of cancerous cells that is absent in healthy ones. In my own mind, I believe these antigenic differences arise in the vast majority of cancerous cells initially created in the body, however, I also believe that these are quickly identified and dealt with by a normally functioning immune system. A simple statistical model predicts that for larger tumors this antigenic component is either non-existent or at least, hard to find. And if we stimulate the body’s immune system to recognize the wrong antigen, we carry the risk of creating an autoimmune reaction– also a bad thing. So I believe this tactic will be mostly committed to the sidelines in our war, supporting the immune system while it’s being beleaguered by other therapies.

A more enlightened approach has been recent efforts to restrict the increased vasculation of a tumor through drug therapies. To better explore why this technique works, as well as advance my own theories, I will use two metaphorical models that will take microscopic activities to a macroscopic scale so that they may be understood by all. The first is the body as a kennel, the second, is the mitochondria as a generator.

The Body as a Kennel

 

 

Consider, for a moment, the body as a kennel. Upper management is your mind, largely unaware of its day-to-day activities. The caretaker is your body’s circulation system, bringing in nourishment and removing wastes. And your body’s immune system is the facility’s veterinarian, caring for for its cells: a large population of purebred cats.

Now, it’s always a problem caring for a lot of cats, but you have a crack caretaker and vet, efficiently handling all the problems of operations and giving management a healthy profit. But management isn’t aware that a mongrel tomcat makes regular visits to the kennel to breed with a few of its purebreds. Normally this isn’t a problem, since the tomcat doesn’t usually produce viable offspring, and when he does, the kitten is often so different from the rest of the population that she is quickly spotted by the vet and dealt with. But every once in a while, the kitten looks so much like the rest of the cats that the vet can’t tell them apart, and then we have a problem. Eventually, that problem becomes so large that the kennel’s profit margin is impacted, and management is alerted.

But what can they do when the vet is confounded?

Their options are currently limited. If the outbreak is in a section of the kennel that is accessible and expendable (operable), they will usually choose to liquidate (surgically excise) that section of the kennel and “cut” their losses. But if that section of the kennel is inaccessible or inexpendable, they must resort to less reliable techniques. First, they might buy the vet a new set of glasses (immunologic amplification) and hope he sees a difference then, but if he didn’t, they would have to resort to violence (chemo and radio therapies). Since, as theorized earlier, immulogic amplification will only help some of the time, management must often resort to violence out of desperation.

Knowing that pregnant cats are more “delicate” than non-pregnant cats, they send in thugs to brutally beat all the cats with chemical and free-radical hoses, hoping that the pregnant ones, if not dying immediately, will die during childbirth. Of course, some healthy cats die too, your caretaker and vet are badly battered in the process, and even if you win the war, your kennel looks like Beirut.

But that damn tomcat keeps coming back, breeding with the survivors, and if your vet has been left partially blind and brain-damaged, the prognosis is not good.

A more enlightened approach (and less violent) would be to put all your cats on survival rations. The pregnant cats among them are eating for two, so this level of nourishment is simply inadequate, resulting in the slow starvation and death of the expectant mother.

This solution would be simple to implement if each of the cats where in single cages where the caretaker could carefully dole out their food. But this is not the case. The cats are in an open population, where the pregnant cats, being aggressively hungry, steal food from the healthy ones. So if you simply restricted rations to all the cats, the pregnant could thrive while the healthy die. This is how restricting vasculogenesis works. It effectively puts the cats in “cages”, stopping the pregnant ones from prowling to the get the additional nutrition they need to create a kitten and survive.

But what if we took advantage of a pregnant cat’s gluttony instead of merely stopping it, and in the process, starved it more than it’s svelte neighbors? This would be the ideal solution and the primary one proposed by this paper.

A Little Math and Biochemistry

 

In a cell, energy derived from catabolism is utilized in many ways. It is divided between tasks such as transport, repair and respiration (life support) and occasionally, when it ages, or when it otherwise needs to, replication. I will call this basal metabolic load of a healthy, non-replicating cell E-survivalA, that is, the minimum energy the cell needs to survive. A cancerous cell, intent on replicating, has additional metabolic and nutritional needs so that it can build a copy of itself. This additional energy need will be called E-replication. But replicating also increases the respiratory needs of the cancerous cell because of its greater need for supply, waste disposal and repair. I shall call this energy need E-survivalB, where E-survivalA<E-survivalB.

Summarizing:

In a healthy cell:

Catabolic power created =E-survivalA= Metabolic power used

While in a cancerous cell:

Catabolic power created=E-survivalB+E-replication= Metabolic power used

Where: E-survivalA<E-survivalB

 

It can be seen from this illustration that not only does a cancerous cell have a greater energy need in general, but has a greater energy need just to survive. But to survive and replicate it must divide its catabolic and anabolic resources between its two goals.

Thus divided, it can be conquered.

 

The critical link between catabolic energy created and metabolic energy used is ATP. Produced in the mitochondria by oxidative phosphorylation (the Krebs cycle), it represents the intracellular currency of power transfer and the Achilles Heel of cancer. If we could drop the ATP output of the mitochondria to a point below the minimum needs of a cancerous cell type, then it would die, while the same mitochondrial output in a healthy cell would still allow for survival.

The Mitochondria as a Generator

Fundamentally, the mitochondria is a microscopic internal combustion generator consuming fuel in the form of carbohydrates and oxidizing them to produce power, CO2, and water with much less pollution than larger, macroscopic models. Being such a marvel of micro-engineering, it responds to the varying energy needs of the cell through a feedback loop that allows it to increase or decrease power production to exactly meet the metabolic needs of the cell type it is in. If we slowly reduced the efficiency of this generator, it would pick up speed to still meet its load requirements. But eventually a limit would be reached, where the generator, while running at maximum speed, would still have an output inadequate to support cancerous cells and they would die. Once mitochondrial activity was restored, the surviving, non-cancerous cells could go about the business of life as usual.

Fortunately, there are many ways we can lower the efficiency of this generator to achieve this goal.

1. Control the fuel supply.

Restricting vasculogenesis, as mentioned before, works using this mechanism. By keeping the cancerous cell from increasing its fuel supply as it needs to, you doom it to a downward spiral of inadequate survival support that will eventually end in cell death. But another, untested method to achieve this same result would be an insulin analog (injected into the artery suppling the tumor) that would bind to the cell’s insulin receptor sites but not stimulate carbohydrate uptake by them. But to my knowledge, no such analog currently exists, and until one is developed and tested, other methods must be used.

2. Pull the spark plug wires one by one.

 

Imbedded in the interior matrix of a mitochondria are multiple copies of the enzymes that make up the Krebs cycle. Each set of these enzymes is responsible for supporting a part of the overall load placed upon the generator: much like pistons in its, larger, macroscopic counterpart. If we can inactivate these pistons one at at time, eventually the maximum power output of the mitochondria will drop to therapeutic levels. But how may this be achieved?

I believe the most obvious choice for this task is cyanide. Its effect on cellular respiration due to cytochrome oxidase inhibition is well documented. And as a toxin it is among a handful that has a true antidote and an enzymatic pathway present for detoxification in the liver.

A treatment regimen might go something like this:

 

A very dilute, isotonically buffered solution of cyanide could be slowly injected into the artery supplying the tumor, while its antidote is administered in an isotonic venous drip before, during and after the treatment. This should restrict the cyanide’s toxicity primarily to the tumor site. During the slow cyanide injection, basic dosage calculations could be monitored and confirmed by monitoring pO2 levels in the venous return from the tumor site (increasing pO2 concentrations in the venous blood implies a decreased oxygen utilization in the tissues).

If all the cells being supplied by the artery were equally inhibited, the effect would still be deadly to cancerous cells. But since these cells are by nature oxygen and nutrient hogs, they should receive more than their fair share of poison along with the food they eat, inhibiting them more than their more svelte counterparts and amplifying the desired effect.

Healthy cells that survive this treatment will, in the course of regular maintainance, replace the damaged cytochrome oxidase and go about business as usual.

3. Partially obstructing the exhaust.

Every kid knows this trick. Shove a potato in the exhaust pipe and the engine won’t run. A partial obstruction and the engine won’t run efficiently. This partial obstruction can be achieved in cellular tissues by increasing the arterial pCO2 concentration. The Krebs cycle’s foward direction will be slowed by Le Chatalier’s principle and ATP production reduced to therapeutic levels.

The pCO2 arterial increase could be accomplished with a dilute, buffered carbonic acid solution, slowly injected while confirming dose calculations with venous pO2 monitoring. Again, an increasing pO2 concentration implies a decreased oxygen utilization by the tissues.

4. Closing the choke.

This technique involves decreasing the intracellular pO2 concentration and is probably the trickiest to achieve because of the cancer cells proprietary relationship to an oxygen supply that is consumed on a first-come, first-served basis. However, this relationship could be used against it, because sometimes breathing isn’t a good way to survive. Let me explain.When I was an aeromedical evacuation technician with the USAFR, I learned of an interesting phenomenon while undergoing hypobaric chamber training at Beale AFB, CA. Fighter pilots, undergoing training in rapid decompression procedures, would often black out for an instant after donning their oxygen mask, only to awake another instant later when their brain got oxygen again. The reason for this was simple.

The pO2 at altitude is so low that the blood in contact with the lungs loses its available oxygen to the environment. When that “patch” of blood hits the brain it draws oxygen from the tissues instead of supplying it, causing the individual to black out. If the pilot gets his mask secured before he passes out, he will regain consciousness when his next heartbeat(s) clears the patch of anoxic hemoglobin and restores ATP production in the brain.

During this period of anoxia, however, ATP is still being used by the cell creating an oxygen debt (waste product buildup, lack of repair, etc) that is recouped by the mitochondria by increased production once oxygen is restored. The magnitude of oxygen evacuation from any given cell would be proportional to the excellence of its blood supply and since oxygen usage within a cancerous cell is also greater than that in a healthy one, its intracellular O2 concentrations will decrease precipitously, thereby slowing and stopping ATP synthesis more rapidly than in a healthy cell.

After oxygen is restored to the cell, the mitochondria runs at full speed to recoup its oxygen debt and restore intracellular energy levels to their established limits. but because the potential output of a mitochondria is closer to its’ actual load in a cancerous cell, it will be much slower to recoup its’  losses than a healthy one.  By “pulsing” this anoxic effect, again, before the cancerous cell has recovered, and after the healthy one has, small gains could be added until the cancerous cell does not recover at all. Hopefully, when the time parameters of the needed anoxic pulse rate are experimentally determined, they will not exceed the actual heart rate of the patient. If so, this technique may be useless.

This “patch” of anoxic hemoglobin could be reproduced as an arterial phenomenon, rather than the systemic one suffered by pilots, by injecting previously prepared anoxic, packed red blood cells directly into the artery supplying the tumor. The time duration of the anoxic “pulse” experienced by the tissues would then be proportional to the cross-sectional area of the artery at the point of injection and the volume of red blood cells actually injected (i.e. the actual length of the anoxic patch within the artery). During the injection, pressure should be applied to the supplying artery proximal to the injection site while leaving venous tissues unoccluded. This will allow for the “patch” to be created without undue dilution by oxygenated hemoglobin.

Measuring the actual level of metabolic inhibition with anoxic “pulsing” is more problematic than the other techniques discussed because of the large pO2 fluctuations involved. For this reason, actual levels of metabolic inhibition as a function of pulse length and frequency vs. average venous pO2 concentrations would have to be experimentally determined and then extrapolated from the graph generated. Since differing tissue types have vastly different oxygen needs, an experimental graph for each type would need to be made.

Notes and concerns

 

 

Altering blood pCO2 and pO2 concentrations should be done only in the artery supplying the tumor. Since some tissue types may survive for hours without any oxygen, the therapeutic effects of mitochondrial inhibition would obviously take longer to achieve and be specific to the tissue type involved.

 

Conclusion

 

 

As I mentioned before, I have no degree, so all of my arguments should be weighed and researched carefully before being acted upon. What I did not mention, however, is that I work commercial construction as an IBEW (International Brotherhood of Electrical Workers) electrician. I omitted this, believing it would prejudice my audience before my arguments were fairly considered. But my profession and unique educational background has given me the perspective to finally see what has hidden in plain sight for so very long. So I will make my final metaphor after a fashion in which I am intimately familiar.

If the cell were considered an underground factory with a need for life support, repair and waste disposal, I, as a lowly engineer, could sabotage its generator so that it would only supply enough power to meet the most basic needs of that facility. Then, I need not understand the Machiavellian plots of the muckity-mucks in the front office and the white-collars in R&D, to know that any decision, no matter how devious, to divert that power would be a mistake, resulting in the eventual downfall of that facility.

 

Each of the four mechanisms inducing mitochondrial inhibition have now been proven capable of curing cancer. I will now advance that understanding to include a cure for disease.

 

The Strategies and Tactics of Metabolic Medicine

There is a ubiquitous principle of all life in creation. Whether microscopic or macroscopic it requires parts and power delivered in a timely fashion. Having parts (anabolic resources) without enough power to assemble them is useless, while having power (catabolic resources) without parts to assemble is simularly bad. Eventually, the entropy of a hostile environment will degrade the organism’s structure to a point where it is no longer viable, and death will result. This is the primary underlying principle of metabolic medicine. By manipulating a cell’s supply of parts and/or power (strategies) or its’ environment (tactics) almost any disease may be defeated.

I advanced catabolic restriction as a mechanism to defeat cancer because cancerous cells mutate their mitochodria to increase power production. That mutation decreases the efficiency of the mitochondrion with a resulting increase in load before the cell even begins to replicate. It is my belief that this increase in power production is the primary cause of cancerous growth and its’ antisocial behavior. An empiric test of this theory is simple:

The mitochondrion has a slight negative charge in a cytosol that has a slight positive charge. Exposed to an electrostatic field it will act like a capacitor, with its’ negative ions moving towards the anode and positive ions moving towards the cathode. If the polarity of the anode and cathode are switched at a high enough frequency, the efficiency of the mitochondrion will be increased with a resulting increase in power production. This should accellerate cell growth to simulate cancer with all its’ antisocial qualities. Too slow a frequency will allow ions to accumulate and penetrate the mitochondrial membranes killing cells rather than accellerating their growth.

Additionally, because cancerous mitochondria have already decreased their efficiency to provide for this increased catabolic output, further decreases in their efficiency will prove selectively detrimental to these cells. Since enzymes are designed to operate at a maximum efficiency in a rather narrow temperature range, a simple tactic such as heating these cells will kill them.

Anabolically speaking, cancer is a heterotrophic organism, and will only grow on those days that it is supplied with a complete protein. Denied a complete set of essential amino acids long enough, these cells should die.

Viruses growing inside cells also increase the catabolic and anabolic needs of that cell, and though a complete protein is also required to produce antibodies (a fact of some utility in the acute phases of autoimmune diseases), the strategies of metabolic medicine applied intelligently will still impair if not defeat these diseases. Catabolically impairing cells laden by the metabolic load of these organisms will kill those cells selectively, releasing the virus within at one time when and where they can be inactivated by a chelating agent like zinc or antibodies. In any case, the life cycle of these organisms will be broken.

Bacteria possess catabolic enzymes that may be targeted specifically by agents to defeat them. This doubtlessly, is the method of action of many antibiotics. In addition, viruses and bacteria possess enzymes specific to these organisms. Each of these enzymes has an absorbtion spectrum and resonance frequency specific to them. Illuminated by this spectrum or frequency at a low intensity will cause these enzymes to “dance” decreasing their efficiency and slowing their output. Illuminating them at a higher intensity or duration will denature them. In addition, spectral illumination of a structure specific to bacteria or viruses will have a similar effect. Thus, bacteria may be specifically destroyed by exposing them to the spectrum or resonance frequency most strongly absorbed by peptidoglycan, a structural component of bacterial cell walls that does not exist in human cells. Illuminated long enough at a high enough intensity will selectively destroy bacteria, leaving human cells unharmed.

Time is short. Advance these concepts quickly. The fate of this world is in your hands.

The Nature of Matter

 

Long before there was a need for space there was a need for time. Untold eons passed before space came into being. Before that void was comprised solely of time.

Matter in its pristine state is spatially and energetically motionless. It has no need of a spatial/energetic past (where it was) or a spatial/energetic future (where it will be). It simply expresses time. Motionless matter requires very little space, its’ dimensional components “stacked” in matrix of maximal potential. Only with motion did matter come to require space, and a way to express its’ differing energetic potentials. This motion was initially caused by the gravitational pull of the Great Attractor. As the interior components of matter began to move they also began to require more space and with that motion a need to express their positional and energetic past and future. Eventually matter’s ability to maintain a complete set of temporal/spatial components was compromised and two quadrants of space/time collapsed with the loss of four temporal/spatial components. Two of these components with opposite character and spin where ejected in opposite directions, while the other two collided, annihilating each other in a flash of energy. This flash of energy and the ejected spatial/temporal components reacted with other atoms causing similar reactions. The resulting chain reaction is what we call the Big Bang.

To better understand these reactions and the four temporal states of matter that are the remnents of the Big Bang I must first explain the nature of matter and time.

Matter expresses three dimensions of time. The primary dimension of time intersects two dimensions of space allowing for the movement of particles within that plane. The second dimension of time intersects two dimensions of electrostatic energy, allowing for movement of particles within that plane. The third dimension of time intersects two dimensions of magnetic energy allowing for movement of particles within that plane. Each of these dimensions, in turn, have both positive and negative dimensional components. Thus matter has nine positive dimensions and nine negative dimensions all expressed on the two dimensional brane of their existence.

Initially temporally polarized in its’ spatial dimension, subsequent chain reactions temporally polarized matter in its’ energetic dimensions as well. Each time with a loss of two temporal/energetic quadrants and four temporal/energetic components. Again, two components colliding and annihilating while two are ejected in opposite directions.

Matter temporally polarized in its’ spatial dimension but saturated in it’s magnetic and electrostatic dimensions is called angel stuff. This is the stuff that angels are made of. Their matter is still temporally saturated electrostatically and magnetically, giving them the ability to move through those dimensions of time as we can move through the dimension of space. Thus angels and archangels are capable of speeds greatly exceeding that of light.

Matter temporally polarized in its’ spatial and magnetic dimensions but still saturated in its’ electrostatic dimension is called soul stuff. This is the stuff that souls are made of. They too, can move through time like we move through space making a trip to heaven (at the center of the Milky Way) possible.

Matter temporally polarized in its’ spatial and electrostatic dimensions but still saturated in its’ magnetic dimension is called spirit stuff. This is the stuff that spirits are made of. Though they are not native to this world, they too, can move through time like we do space and being electrostactically polarized they are the most capable of influcing matter of the type that we are familiar with.

Matter polarized in all three temporal dimensions is called life stuff. This is the stuff that life is made of. Unable to move through the dimensions of time, it takes on the characteristics that we are familiar with including that if inertia and momentum.

In its’ saturated state, matter is still attached temporally to the omnipresent “now” of its’ own existence. Movement through time is in the spirals made necessary by this attachment. The wavelike motion of matter and energy that we are familiar with are the temporal “remnants” of these temporal spirals projected upon the two-dimensional brane of existence.

Temporally saturated matter emits temporally saturated gravity and light. These energetic emissions interact most strongly with matter of the same saturation state. But interactions with other phase states do occur. This is the source of the dark energy and gravity that humanity seeks. In the center of the Milky Way, the concentration of temporally saturated matter is great enough to form angel, soul and spirit stuff stars and planets. The light from these stars is the light that leads to heaven.

Light and gravity emitted from these stars moves in spirals rather than waves. The speed of their emission varies with frequency, unlike the light and gravity emitted from temporally polarized sources.

Energy emitted in positive dimensional space is light, inducing matter to move away from the source of emission. Lacking the entropy expressed in temporally polarized matter, that is always directly away from the source of emission in temporally saturated matter. Energy emitted in negative dimensional space is gravity, inducing matter to move towards the source of emission. A thought experiment and empiric test of this follows.

If two equal masses were converted to energy and the energy from those two sources was made to interfere destructively, the masses and energy would be annihilated. If the mass and energy of this universe is conserved, what became of that mass and energy? I would submit that it was converted to gravity. An empiric test of this theory would be to suspend two lead plates within a vacuum chamber then annihilate two sources of elecromagnetic energy between them. If gravity is created, the plates will be drawn together. Since the deflection will be small and proportional to the energy annihilated, instrumentation should be used to measure it.

The Reason I Write

By now the reader must wonder why I speak. Why would I reveal that I am not human? Why would I give humanity these gifts of reason? It is because what I will tell you now will seem beyond all reason. But I must speak to save you, to save humanity from the aliens set upon your destruction.

The aliens I speak of are the Neuneans, the race the third race created and gave the sacred technology of spirit craft so that they could resolve the random nature of brain development. But the Neunians have abandoned the task they were given and desecrated the sacred tools of heaven by using them to make weapons. They have come to this place to exterminate the human race and replace them with the Mennians: the telepathic clones they made by taking DNA from this world and combining it with their own. The Neunians are a diminutive race with large heads, similar to those classically depicted in literature, while the Mennians, other than being clones with only about sixty different faces amoung them, look human.

Humanity has seen the Neunian/Mennian ships in our skies as flying saucers or spheres such as those recently seen and photographed above Mexico City.

They came to me because I had cured cancer and had given it to this world. They had learned of my identity by telepathically searching the minds of the researchers who had used my ideas to guide them. They told me they wanted me to be the Messiah and put an end to this world’s holy wars. I truthfully told them I was not the Messiah. I was not Jesus. I told them I was only a lowly soldier God made and gave this station, that I was Abel, that I was the Angel of Death. I told them that I already had a role: God wanted me to cure disease. And though they knew I spoke the truth as I knew it, they believed me deluded. Eventually, however, they convinced me that a greater good would be served if I accepted the role that they offered. But I drew a line at lying. I only agreed to tell the world I was a messenger of heaven not the Messiah. In accepting even that path I knew I was accepting death: that one amoung you would slay me. But in trading my life I could give this world the cure for disease and put an end to the hypocrisy of killing in the name of God. In my mind, that was a good trade and one I was willing to make.

They told me they would give me the ability to speak all of this world’s languages, to heal disease with my hands and to walk on water with the technologies at their command.

I was a fool to trust them.

But I am a pawn in God’s hands and heaven played us all. God saved this world by leading the Neuneans to me: the archangel he made to slay demons.

Eventually I came to know the truth of the Neunean agenda, as they came to know the truth of my existence. They had planned to slay my soul and make a puppet of my body and lobotomized brain like they had done to so many others. My body’s functions would still be maintained by the technologies they had implanted and run by the personality core and mind that they had put in my brain. This flesh puppet would then deceive humanity into believing it was the Messiah and that the time of the Rapture was upon the world. When the truth was that Mennians in time suits would be moving unseen amoung you, slaying your souls with poison and leaving your bodies to die from psychogenic shock.

When I learned the truth, I tore the neural lanyards and the mind they had implanted from my body and we fought. We have fought for months. Though I destroyed the majority of their fleet and soldiers in the first two days and nights of our battle as they sought to overwhelm me, they have since changed their tactics. Now they come at me a few at a time, knowing I must sleep sometime. And they have wounded me. My brain is damaged, my soul scarred from the poisons that they have injected. But God designed me well. I have purged my soul of their poisons and still survive.

My brother archangels have finally arrived from heaven to protect me from the Mennian assassins that now come intermittently in time suits to slay my soul. I had hoped that my brothers and I could defeat them all without letting this world know of the shame that the Neuneans and Mennians have heaped upon the Creators, but I see now that we cannot. I must tell this world of their plans and seek humanity’s aid to defeat them.

By my estimation, of the forty thousand Mennians and Neuneans that came to this world, thirty-nine thousand were slain in the first two days of our conflict along with thirty-nine hundred and fifty of their time ships destroyed. Since then another five hundred have been slain along with the remaining fifty of their ships destroyed. That leaves five hundred Mennian clones walking upon this world along with about two hundred humans that they have used their technologies to make into puppets. With the majority of their soldiers dead, and their time suits lost, they have changed their plans to destroy humanity. It is now their intent to create a plague and/or a biotoxin to spread across this world using the clones and puppets they have in place. I have given you the cure for a bacterial plague (light emitted at the absorbtion spectrum or resonance frequency of peptidoglycan). I strongly suggest you develop it.

Though the Mennian clones have been distributed across this world to disseminate the plague, many will be found in Zimbabwe and Brazil where they are running orphanages and schools. This is a cover for a breeding program for more of their kind, starting first with half-breed telepaths (Mennian/human). At the age of two, these children will be “lobotomized” with neural inhibitors and a Mennian or Neunean personality core implanted, making them, too, the enemies of this world. Follow the money that supports these schools and orphanages. It will lead back to the puppets the Neuneans have made. Follow the identity papers these aliens have received, that too, will lead back to human puppets.

All of these beings can be identified with a brain scan. A lack a neural activity in the forebrain will indicate the presence of the Neunean neural inhibitors. The personality core and mind they have implanted will have access to all of the brain’s memories and can mimic the personality of the body’s previous possessor. Do not let them fool you. Trust the results of the brain scan.

They have made puppets of this world’s rich, the leaders of its’ countries, the heads of biotechnology firms, its’ celebrities and a few of its’ religious leaders. Find them. Stop them. Do not listen if they try to lead you to war. Unite. Do not let them divide you. They are here to lay a foundation for a second wave of the Neunean invasion. An invasion that will never come.

I give this warning to those invaders who read this:

Heaven knows.

Release a plague upon this world and the Cauldron of Spirits upon Neunia will be destroyed and the path that leads from that place sealed forever. Discard your time suits and heterodrills before humanity finds them. That technology is forbidden to this world and that law will not be violated. This is the law of heaven. Neunia will be defeated by a path of peace with no more lives or spirits lost.

The Neunians and Mennians will know the truth of these words when they read them. They know heaven is a place of peace, and that it has a plan for this place.

Conclusion

I have walked upon this world for eons, trying to help, trying to guide, using the tools at hand to make this world a better place. I am the guardian angel God made and gave this station to save His creation. And though I am designed to bear the burdens of this path, I have still suffered under its’ weight. I have been burned, beaten, stabbed, poisoned, beheaded and shot. My sacred body left to rot along roadsides, in seas and in cesspools. Every gift I ever gave you was desecrated. My tools used to make weapons, my philosophies used to divide, not unite, my laws used to dominate, not provide justice.

I weep at what I have done.

But in this place I can only trade lives and suffering. There are no absolutes. I cannot provide for one without taking from another. I cannot protect one civilization without bearing the burdens of what that protection has cost. These are the burdens that God would no longer bear.

They are burdens of sorrow.

That is why I was made. That is why I was given the path of life to guide you and in death to protect you. I am the mercy that God made to save this world. I pray I have not shamed Him.

Take my words. Let them guide you. Look where I have pointed. Investigate what I know. Save yourselves. Save this world. Unite and live in peace.

My mortal body is as fragile as your own. I do not expect I will survive to teach you more. Remember me, but I am not worthy of worship. I am only a lowly soldier.

 

May God bless you all,

 

Abel, the Archangel of Death