Breakthrough! TransDNA Explains Cancers and SIDS

[Bruce D McKay Elijah]

For Immediate Release ​

Breakthrough! TransDNA Explains Both SIDS and Cancers!​

Helicobacter pylori and a TransDNA, a spontaneous recombinant DNA from this bacteria, can be shown to explain both Sudden Infant Death Syndrome (SIDS) and the various forms of cancer!
This is a stomach bacteria you will find that was put on a list of carcinogens in 1995, by none other than the NIH.
(See Science, Vol 267, 17 March, 1995, page 1621.) Researcher, Bruce D. McKay of Tampa Florida, after working on this problem for more than thirty years, has finally solved the riddle of both SIDS and cancers. He says, both cancers and "Sudden Infant Death Syndrome are caused by the same type of DNA from bacteria, and in SIDS that DNA is frequently from the Helicobacter pylori bacteria. The anwer to all this about what was causing cancers and why do babies die of SIDS," he explains, "has simply escaped detection because the 'mysterious agent involved' has always been a tiny amount of TransDNA, from an almost unknown, drug resistant bacteria - being processed without any fanfare whatsoever! And the incoming, infective form of TransDNA, was simply being transmitted from a relative, a visitor, or a care taker - and that someone was a direct parallel to those persons that were well known in the early 1900's as TB carriers!”

"DNA transfer or 'TransDNA activity,'" says McKay, "is as common place to the world of drug resistant bacteria, as are automobiles running up and down a busy interstate expressway. But few persons know that this same TransDNA activity is the mechanism frequently and repeatedly exercised by all of the drug resistant bacteria! The medical community never caught on. They never recognized it being in operation. They never figured out there was DNA that existed in a rapidly moving, spontaneously transferring form. But they did experiment with the other, slower and 'fatter forms' of DNA, which left them for the most part with the opinion that most bacteria did not even transfer DNA. In most instances, everyone thought of it all as if evolution ran all types of drug resistance. As one researcher put it, the "assumptions behind today's medicine are left over from the turn of the century, when science was forcing dogmatic religion to see the evidences of evolution."* "This is basically why, on the whole, almost every member of the medical community yet thinks that all the antibiotics are somehow ‘loosing their touch,’ or otherwise loosing their effectiveness. But at the same time none of them can ever tell you why the whole bunch of antibiotics that were all once so higly effective, now have no punch at all in a great number of cases!"

McKay says the reason for this, is the answer that everybody has been trying to find. "Basically, the bacteria have been growing stronger and stronger as a result of their being able to overcoming the antibiotics by their own TransDNA activities(!) and they typically exchange DNA's and transfer an all but invisible form of very clear DNA. What also made it 'so hard to catch on to' is that this form of DNA is so clear, that it is microscopically undetectable - yet it even accounts for the deadly toxins that bring about something like SIDS. The reason for this is that the unfortunate victim simply did not have an adequately developed immune system. The mysterious agent involved has always been ‘TransDNA’ - and it was passed to them by someone, much like a TB carrier! The unfortunate small children succumbed to the 'secret agent DNA’s' so rapidly, they were quickly and completely overwhelmed by the toxins, because the toxic reactions were moving so fast that there isn't even any tell-tale scars left behind that anyone could ever find!”

“The one 'other way' it works," he says, "is that some strains of these same drug resistant bacterium are also able to replicate various drug resistant genes - and then they can transfer that "drug resistance" (i.e. the drug resistance genes) into another cell. After a while, those DNA's ends up (i.e., being found later,) as the driving force behind amost every form of cancer and every tumor! The cancer causing power and the tumor causing power of this form of DNA comes from the fact that it can carry the self-replicating DNA modules that enable it to replicate again and again! The TransDNA's is transferred and taken up almost spontaneously, and it can even pass itself independently to other cells when it has certain 'self-transfer DNA modules' included. Researchers have proven that it needs NO chromosomes present to do this. Nor does it need any of the bacteria being present, from which it originates! Therefore, the uptake of this form of TransDNA by a cell fully explains both neoplastic cells and metastasis. And when the self-transfer DNA modules are not included," according to McKay, "that accounts for the major body of charastices that we commonly refer to as (non-malignant) tumors." He says, "Now that explains how the Helicobacter pylori ended up on a list of microbial agents that are classified as carcinogens by the NIH – and almost the whole story is right there - in the March 17, 1995 issue of Science."

Mr. McKay has also found and it is his own discovery, that ordinary cells in a given tissue have the same TransDNA system working in them too! “The research community never gained sight of this fact,” he says. “Then, in 1981, Griffin and associates noted that there was a great ‘heterogeneity’ among normal cells after they were dispersed from one another and grown in culture.” ** McKay says, “What they found is that the cells they were studying would suddenly take on a totally independent nature or an entirely differing manner of activity(!) each time they were broken apart and placed in a culture! This is simply because that’s when they would loose the TransDNA mechanism that normally links everything up, from cell to cell.” As he explains it, “The cells normally transfer DNA from one cell to another cell, but all of that is readily lost when the very delicate microtubules that bridge from one cell's membrane proteins to another are disrupted and the cells are otherwise torn apart. That is what happens, simply as a result of placing most cells in a culture medium."

Absolute proof. “For the absolute proof, go and look in any biology text book yourself, and you can easily prove it to yourself,” he says. "Just look and find about any good model of the cell. When you find it, look closely at what you see present on the cell’s surface as a 'membrane protein.' Now, just below that and you should find some tiny little microtubules running from the membrane protein, down to the very heart of the cell, straight to where the chromosomes are, or the cell’s DNA. Now to see what's going on, go back up where the microtubules meet at the membrane protein. That is where the microtubules pass out of the cell. And from there they bridge to the next cell's membrane protein. This is what ‘hooks together’ all the cells in a given tissue, at the DNA level - and so it readily proves the whole thing! In other words, to correct 'the static nature of the cell theory,' the third statement of the Cell Theory sould actually be something like, 'The cells that make up any given tissue, are connected by almost invisible strings of very fine microtubules, to all the other cells, and this provides each given tissue with a highly specific network of intercooperative control at the DNA level.'"

This thing about cells all acting independently when placed in a culture, also readily explains what has perhaps truly hindered and hampered all of the medical research ever done on almost any gene-related disease or any form of cancer. McKay says, “The researchers were never comparing apples to apples!” “It also explains what causes the drug resistance genes to emerge as they do, in almost every cancer and every tumor - regardless of the tissue or origin. And it as well explains, what lays just behind many other diseases such as MS, MD, Diabetes, AIDS, HIV, and a wide assortment of other gene-related diseases,” according to McKay. In that regard he says “all of those diseases would be just like cancers - if the DNA modules for self-transfer of the DNA had been included, when the disease was first being initiated! The well hidden TransDNA mechanism," he says, "is an intrinsic part of all nature. The evidence and photographs of microtubules linking cells to cells, and is available for further study, analysis, and evaluation, on the net at... thecancerdiscovery.net.

"Nor are the findings that surround the ‘TransDNA’ as a spontaneous cancer causing recombinant DNA, difficult to comprehend, or explain. All the otherwise unwise critics and perhaps a few of the best professional researchers around may at first take their shots at this, but once anyone has become aware of what it is that is truly going on, everything begins to fall into place," according to McKay. “The major problem has always been that the TransDNA being passed or transferred into the cell is so light that the electrons from the electron microscope pass right through it. The scientists that experiment with recombinant DNA’s know of it. They have explored it’s presence. They have even classified it as an r-plasmid, or a form of 'resistance gene' transferring DNA – without ever making the realization that it was not just some kind of orphaned thing. But that’s partly because just a shadow of could ever be seen, and even then it took high speed photography and "metal staining" just to see the shadow of it. So no one ever realized it was part of the a super large, spontaneous control system, so extensive and so immense that it actually regulates the ongoing DNA activity of almost all of the entire body of nature! In other words - what was going on was far to big for anyone to see! And the TransDNA's were causing the various "drug resistant disease" and the "gene related diseases" simply as a result of the transfer of drug resistant genes, (or plasmid-like DNA) with its own self-transfer properties and other recombinant DNA factors being ‘pasted in.’ Then that was being passed into a system of DNA control - that is already in full operational within a given cell within some tissue of the host, which was often, more or less 'closely related' in all actuality, to the bacteria of origin.

This briefly explains how "drug resistance genes" end up as suddenly emerging in cancers and tumor cells – when the same cell from any similar tissue or some other host, doesn’t have this same feature in any manner, shape, or form. Now if you would like to help stop cancers and many other diseases, please make a copy or copies of this press release and publish it, print it out, write it up, or send it out - to any of your friends or anyone in the media. Or, 'copy and post it' on any of the popular net boards or forums. By doing so in the very near future these findings may provide a whole new paradigm or a new scientific basis of logic for the entire medical industry to more successfully address and study cancers and tumors. By doing so – we will all be very rapidly moving one step closer to both better learning and better understanding how to otherwise shut down or defeat almost every cancer and every tumor, and many of a great number of the other so-called "gene related diseases."

Bruce D. McKay, Epistemologist ____________
Date: May 26th, 2004 ________________ ​

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*Becker, Robert O., and Selden, Gary, The Body Electric, Quill, New York, 1985, page 20.

**Griffin, J. E., Altman, D. R., Durant, J. L. and Wilson, J. D., "Variation in steroid 5a-reductase activity in cloned human skin fibroblasts," J. Biol. Chem., 256: 3662-3666, 1981.

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For more information, please contact:

Bruce D. McKay, Epistemologist
11308 N. Hamner Ave
Tampa, FL 33612

(813) 933-4905