Cancer Finally – A Strategy That Will Work
CANCER
Finally – A Strategy That Will Work.
by
Francis William Andres II
and
Frank W. Andres
© Copyright Francis William Andres II, Frank W. Andres 2024.
All Rights Reserved.
Fire Mountain Publishing
4075 Vineyard Ave. Pleasanton, CA 9566
Please visit our website at http://www.cftheater.info
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Introduction
Things seem fairly straight-forward to us. Very simply our idea is this: Cancer is not a disease in the usual sense. In the usual sense: Disease is caused by some foreign agent. A virus or bacteria is attempting to kill a person. In the case of Cancer – our thesis is this:
When it comes to Cancer – there is a foreign agent – an embryo. One does not usually think of a baby as one’s enemy. A baby does have its own immune system. It must learn to distinguish between its body and the body of its mother and know which parts of the mother are compatible with its arc of development. There is a counterpart to this of course – which becomes quite interesting. A mother’s body becomes accustomed to an embryo – a foreign body existing within her. Perhaps part of the problems with finding a cure for cancer is related to the fact that a mother is induced by biological factors to tolerate aspects of such a foreign body residing within her and even support it with nutrients. This produces differences from a normal disease. And it simply calls for: A different strategy.
The crucial moment for us was when: One of us remembered seeing a drawing of a Cancerous glob of tissue in one of the references he had consulted some thirty years before. In that glob were drawn what an investigator had seen and a reader could not forget remembering: A mass of cells mangled and tangled. And in amongst that mass of monstrous destruction were certain identifiable objects: Hair, teeth, bones! Right then and there with that remembrance – one of us right now – saw the answer to the question: How can we cure this horrible disease? Well, this tangled mass was obviously a baby. A baby was attempting to grow where it had no business – or ability – to do so. This leads to a different strategy for a cure for Cancer. It leads to an obvious mantra – a chant to be intoned again and again: Simply Kill Kill Kill!
In this minibook we are using the word ‘embryo’ in a broad sense:. The single-cell organism resulting from a fertilized egg is a zygote. When the zygote divides to become a collection of cells that can implant in the wall of the uterus, it first moves down a fallopian tube for about a week – during which time it becomes a monula, and then a blastocyst. About four seeks later, after the development of an amniotic sac, it becomes an embryo. Ater eleven weeks, it is usually referred to as a fetus.
Cancer as Polio
A History of Failure
OK: So up to this point in history Cancer has been seen to be simply: A disease. It has been simply a question of: Which vaccine is to be developed. Well, one cannot blame therapists and doctors for attempting to fight Cancer in the way they have done – in the past: In most cases – for most disease – a vaccine does – the job. A vaccine is created by using the disease itself. If it is polio – the virus that infects one with polio is captured and killed. These dead cells are then used in the vaccine to cure the disease. These dead entities when injected into one – stirs his or her immune system to action. The dead cells alert the system as to which pathogen to look for When such pathogen is found – the vaccine has a poison that kills it.
Vaccines have been used for a long time. Cancer research using them started in earnest around 1980. There was virtually no success using them against Cancer until around 1990. And even then progress was questionable. In the 1990s a strategy involved monoclonal antibodies was developed. This strategy utilized tiny man-made instruments. These man-made antibodies – each one could identify a specific antigen or pathogen – with its upper part – and then it had the equivalent of a poison in the lower part to dispatch the culprit. This strategy was pursued until around the year 2000 – when it was discontinued – with little total success.
Vaccines using RNA
The human genome was delineated in the year 2000. Scientists could use their knowledge concerning Deoxyribonucleic Acid (DNA) now. Many of these scientists decided to work with Ribonucleic Acid (RNA) instead. RNA would seem to be like a sister to the more Powerful DNA. The Truth is: RNA came first on the ladder of evolution. It appears to have held the first form of Life! RNA can be snipped up and used to do things without damaging the original template: DNA. It is simply safer to use. Also it is the molecule that gets things done: Its job for the three plus billion years after its appearance – has been to duplicate portions of DNA and put them to work making proteins that are needed for a cell to Live.
So: We know what typical vaccines do. Please see above. Well: Vaccines using RNA in effect are doing exactly the same thing – pursuing exactly the same strategy – that is pursued using the usual vaccines. It is also sort of trying to duplicate what was done with monoclonal antibodies. It is forming/ creating the equivalent to antibodies to combat foreign agents that have entered a person’s body. It is just that RNA can be used to augment an antibodies’ Power and longevity.
In March of 2020, COVID was shutting down universities and other establishments. There was evidence that protocols using the usual antibody vaccine route were not working effectively against this disease. Fortunately a gene-editing tool called CRISPR – part of a RNA enzyme editing- protocol – which was developed in 2012 was at hand to be used in an experimental way to help battle the disease. In this way a tool that was developed partially for the fight against Cancer could gain some challenges and indeed some improvements from its use in this new battle against a formidable pathogen.
So: The historical use of vaccines is based on techniques that were found essentially through the process of trial and error. As we say: The important date now was the year 2000 when the human genome was fully delineated. This string of code contains all the secrets of Life. As we say: Some scientists initially were focusing on the DNA itself and unraveling its mysteries. As we say: Others were looking at its sister – actually in terms of evolution as it is vaguely reconstructed for the cell – RNA was DNA’s mother – as RNA existed before DNA – and actually may have represented the first: Life! This second nation-wide collection of scientists were looking at RNA.
It turns out that bacteria were using RNA – billions of years ago – to fight their perenniel foe: Viruses. Scientists now were understanding the totality of what these nuclear molecules could do. First, they could be used to fight disease – as bacteria have done for billions of years. They can seek out viruses, enter them, find their genomes and use RNA to slice genes to pieces. Some scientists saw another possibility. They could use RNA in human cells. Changes could be made to human DNA, repair damage caused by mutations, perhaps add genes that can do things – all of which opened the possibility of entirely new Lives for human beings – free from disease – full of vibrant Health! In all this there also arose: Caution. Fighting Disease is one thing. Enhancing – changing human beings genetically – physiologically – in ways that can be inherited – is fraught with ethical conundrums.
Still – when it came to disease: There was a new tool: RNA. However, the same basic therapy – the therapy that was initially used against Polio – was still in place. A pathogen was identified and action was taken to disarm the threat. Several variations to this theme had been tried by the year 2010 – and nothing seemed to be working – in the fight – against Cancer.
What in the Heck is – Cancer?
Our hypothesis is: Cancer is the making of an embryo! It is simply is being done – in the wrong place. This is the result of a mutation in a gene. This mutation of a gene takes place in a genome of a cell that is in no way prepared to support the growth of a baby. The cell in question may be in one’s arm. So: In a way – Cancer does indeed involve the invasion of a human body with a foreign agent. However, this foreign agent does not have the intent to harm its host. In fact both agent and host suddenly are persuaded to start participating in a cascade of physiological and biological events that usually climax with the birth of a baby. In this case things go wrong. Very very Wrong.
There are differences of course – in the course natural embryonic development versus what occurs with a Cancerous growth. If this is a normal pregnancy we are talking about: Doctors do one set of things.
When it comes to Cancer – doctors simply must work differently. With Cancer: We simply are not polite. We are not pussy-footing around. We are simply: Out to . Kill . And Kill – for Good!
Normal Embryological Development
Let us review what happens it the first days of a normal embryonic development. An egg is fertilized by a sperm. This creates the first cell that will eventually become a child. The child has a genome and the mother a different one. The development of the embryo is driven by the genome in the embryo. The genome in the mother acts in a reactive – responsive way – it is induced to support this development
When comparing normal embryologic development with its Cancerous counterpart – the most similarities occur during the first days of development. During the first five days the fertilized egg becomes a zygote. During this stage the zygote divides five to six times. At the end of that time: The zygote becomes a monula. This monula then moves for about three days through a fallopian tube – to the uterus where it becomes a blastocyst. In this way: For three or four days this original cell divides three or four times until it consists of 16 or 32 new cells. At this point: This cluster of cells attaches itself to the lining of the uterus.
Up to this point: the development of a normal embryo and one that will erupt into Cancer are probably very similar.
Cancerous Embryonic Development
So: As we say – Cancer begins with the fact that an embryo is simply not a part of one’s body. It is – actually an intruder of sorts. One does not think of a baby as an enemy. Yet a baby possesses an immune system of its own. It must be able to distinguish its body from that of its mother. This is not necessary to stress – but Life was created by Hydrogen ions working together in a primeval ocean. The real secret to their success was the creation of a map in atoms – in which was inscribed the ability for Life to be: Well – aLive! And then to be able to reproduce.
It is the reproduction part that we are concerned with here.
When we talk about Cancer and embryonic development – things get a bit confusing here. This confusion is part of the difficulty that leads to Cancer. As we say: An embryo is a foreign body developing within a ‘mother’s’ body. The fact is: This may not be a mother at all. This can occur in any human being at any time at any place in his or her body. Well: Every cell in a person’s body possesses the same genome. This means that if one selects a cell in your arm and examines it closely – it possesses a genome. And then you realize: The genome in this particular cell is exactly identical to the genome that created you – in the first moments of your existence. This genome – located in your left arm – is identical to the genome – that created your embryo – at the very beginning.
At the very beginning: An egg is fertilized to form the first cell of an embryo to be. This fertilization initiates a cascade of embryonic development. In the situation for Cancer: A mutation in a genome of a cell in say one’s arm – initiates this same cascade of physiological development. This time: In the wrong place.
As we say: There are probably only slight differences between what a Cancerous zygote experiences and what a normal zygote experiences – during the first week of embryotic development. After that duration: We can expect wildly different development. When we zero in on the development of a Cancer cell – we can see that divergences from normalcy begin at the point when the embryo is supposed to attach itself to a mother’s uterus. That cell in one’s arm is not naturally primed to divide – rapidly and continually in the way an embryo is. The cell in one’s arm has its own work to do and this work is now is being pe-empted by embryonic behavior.
So: A mutation has occurred in a cell in one’s arm. This cell will now experience a cascade of activities prescribed by the genome that this cell and all subsequent cells that are generated – share. There is the cluster of cells that are generated from the arm cell turned into ‘embryonic’ cell. Then there are the cells surrounding this cluster. Well, these cells share the same genome as the ‘embryonic’ cells – but there is no mutation within them turning on a ‘mother’s’ automatic response to this embryonic cascade that is going on in the embryonic cluster of cells. Thus after the first week – the ‘embryo’ is pretty much on it own. It is a growing embryo in an environment that is foreign to it and is not supportive of it – in any way.
So: The Cancer embryonic cell is dividing!!! Rapidly. As we say: This is crazy for a normal cell – in one;s arm! So when a scientist is looking for first signs of Cancer – he or she may see first – signs of cell disfunction. Whatever the cell’s original work was – this work is now being curtailed.
Now in all of this: Our first objective is – to catch things before they spread. Spread from what? Not spread from one cell. This embryonic cell in one’s arm – now becomes a sort of moving target. One cell become 16 maybe 32 – in just a matter of a week. It is this cluster of cells that now resides in one’s arm that must be detected and dealt with as soon as possible. But this remains principally conceptually the same as: Deviations from one cell’s behavior at this point. Technically: Cancer has not spread yet.
When a baby is in cells in our arm – it is a problem. So there are two genomes in a normal situation – there is a genome in the embryo in the uterus – and the genome in the uterus itself . The embryo is a foreign agent that a mother’s genome has to be induced in a complicated manner to at first tolerate and then support. But in the case of Cancer: There actually is only one genome – there are two identical genomes – one in the cells of the embryo and one in the cells of the arm. This is probably the reason that the Cancer is not immediately aborted. All is compatible. All seems in a sense to be fine. Even though things are drastically wrong! One’s arm is simply trying to build or it is allowing to be built – a clone of the individual who is suffering from this Cancer.
After a week this cluster of cells is too small to be detected easily. Cancer must spread before any distinct signs will appear. Unfortunately – at that time – when Cancer is spreading: Cancer is well on its way. We must devise a way – to identify the presence of Cancer – early.
An embryo is basically assembling itself using the DNA in the cells that are dividing. The embryo is relying on cues – physiological cues – that it obtains from the environment around it. The cues that the embryo receives from a uterus are vastly different from cues that an embryo receives from one’s left arm. These differences are crucial to our strategy for a cure. These differences lead us to one conclusion – seldom pronounced during the present time to deal with Cancer. Our mantra is simply: Kill Cancer. Kill Cancer.
Towards a Successful Strategy
Cancer in the Embryonic Stage
So – we can see: After about a week – the development of Cancer must pause. It has gone through roughly a week of cell division. It continues to divide – but now it is looking for physiological cues that it would normally receive if it were actually attaching itself to the lining of one’s uterus. Physiological cues that a embryo would receive from all directions at this point – are simply – not forthcoming. Because of this – development of this Cancer embryo – just stops. This can give us some time to react – and Kill.
So how can we use this precious time? We shall only have two or three weeks in which to work quickly. Well, we need something like a equivalency to a colonoscopy. And we need to do a thing like this for everyone – every month! Cancer can start in anyone – at any time. And in every case we need to stop it Bang!! In its first month. Everything is very very tiny at this point in time. There is little physical indication of deviations from the norm. There is no pain. What we need is a test. It needs to be one – that can be used monthly and not be a burden to anyone.
Well, one idea comes immediately to mind: A sort of pregnancy test. It could even be developed such that it could give results for a real pregnancy as well as tell if one is with or free of Cancer. If the test discovers evidence of embryological biological behavior: You are pregnant! If the test finds evidence of such behavior and also discerns the existence a protein or two related to Cancer – then sorry – you have an embryo – growing – in your arm!
So one possibility of action that could be taken every month is – like a normal pregnancy test that is taken by both sexes. This could be made more palatable – by being a saliva test.
When results are positive for Cancer – then patient and doctor must act and react immediately. But there are as yet no overt signs of Cancer. OK: A person has Cancer. Where are these almost invisible cells located? They could be anywhere throughout the body. Anywhere! At this point personal family histories must be scrutinized. Which sort of Cancer is this person susceptible genetically to/with? Armed with this information: Tests should be performed immediately -that are usually not performed until very late – too late – in the game. When physical evidence reveals the location of an embryo growing in one’s arm: Well, Kill!
Every doctor is now aware – that every genome possesses a Kill gene. Once the general area in which the tiny Cancer bundle resides is located – an injection should be made – with that Kill gene in mind. The location of cancerous cells can be zeroed in on more accurately by the identification of markers in cells. For example when an embryo is unable to attach itself to a uterus: It is unable to create an amniotic sac – which will become a placenta in which to continue growing in a normal manner. A placenta is one thing that is always a part of a baby and is not a part of the mother. The embryo will attempt drastic measures to create such a biological envelope. When it fails there may be evidence of that failure: Pieces of placental fragments in and around the embryonic cells. When such fragments are identified in and around a cluster of cells – these cells must simply be Killed. This is the equivalent of radiation treatment but practiced much earlier – in much a more exacting fashion.
Cancer Later On
The above is a proposal for a therapy that can work when Cancer is caught in the first month. We need a theory for later on – in cases wherein Cancer is allowed to develop – when a small bump is found. Well, generally speaking the same approach that practiced today – should be taken. If the Cancer is still in one lump it has not yet spread – hopefully an injection can be made with the same Kill objective in mind. This can be supplemented with the usual therapies that are used when a lump is found – In case a few Cancerous cells are missed.
Finally we need a therapy when Cancer is spread and is rampant. Well, the same desperate measures that are now used are called for here. But supplemented with repeated attempts to Kill Kill Kill !!!!!! using those always present and extremely effective Kill genes.
Conclusion
Cancer has been an affliction that has been able to avoid all efforts to identify and eradicate it. We think this is because the True nature of the affliction has not been recognized. Cancer is not a typical virus affliction toward which all existing therapies are now directed. Instead: It is the appearance of a very normal physiological process occurring in a very abnormal physiological place. Cancer is the not result of an outside intruder attempting to kill a person. Instead it is a very normal set of genetically programmed steps in a biologically normal development – that is simply occurring in the wrong place. This is due to a mutation which has caused a cascade of biological steps to take place in the wrong physiological setting. A successful strategy is just simply: Kill Kill Kill !!! Cancer. Well, the aim of our proposal for a therapy is: Not to pussy-foot around – not merely sit around and attack pathogens – splice this or dice that. As we I say: This strategy has one aim: To Kill Cancer cells. And the simple fact is: This Killing is easy. Every human cell possesses a Kill gene. It is surprising that this gene is not activated routinely – early in the game. The fact is: it isn’t. So our strategy becomes simply: Identify which proteins are products of Cancerous action, find cells that possess such proteins in their output. And then simply Kill those cells. One by One.
The trick is: In its earliest stages Cancer does not exhibit Cancerous type of markers, proteins , hormones, or molecules. Cancer at this state is simply an embryonic phenomenon. It is one – that simply must be identified to be happening – then be stopped – Now!!!
It should be noted that the embryo developing in one’s arm was never a normal zygote. There was never an egg which was fertilized. Therefore it will never possess anything like a normal Consciousness. It will never develop into anything resembling a normal Living – sentient – Being. It shall always remain simply a mass of cells – programmed to divide and divide until the human which is its host is finally dead. So one must not have qualms about Killing what might be some sort of baby. This is indeed a monster we are talking about. But it possesses no Consciousness. It is a some sort of zombie disaster. Treatment is simple and straight-forward. One must simply identity Cancerous cells. And then: Kill. This is indeed – a Fight – to the End!
Kill. Kill. Kill.
THE END
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