Category Archives: Virus

A Second Thought About Viruses, Vaccines and the HIV, HPV, HEP C, Measles, Mumps, SARS, Hantavirus and Ebola Hypothesis

Micrograph of a solidification of metabolic acid
Parasite or Virus?
So-called Ebola Virus or Parasite?
A Second Thought About Viruses, Vaccines and the HIV/AIDS, HEP C, HPV, Polio, Spanish Flu, Hantavirus, SARS, Measles, Mumps,  and Ebola Hypothesis! – Part 1
“In the sciences, people quickly come to regard as their own personal property that which they have learned and had passed on to them at the Universities and Academies.  If, however, someone else now comes along with new ideas to contradict the credo (that has been recited for years and passed on in turn to others) and in fact, even threaten to overturn it, and all passions are raised against this threat and no methods are left untried to suppress it.  People resist it in every way possible: pretending not to have heard about it; speaking disparagingly of it, as if it were not even worth the effort of looking into the matter.  And so a new truth can have a long wait before finally been excepted.”  – Goethe
Viruses
 
Introduction
The first isolation of the virus was achieved in 1892 by Russian that bacteria hunter Dmitri Ivowski, who gathered fluid from disease , tobacco plants.  He passed this liquid through field for fine enough to retain bacteria; yet to Ivowski’s surprise, the bacteria space free filtrate easily made healthy plants sick.  In 1888, a Dutch botanist, Martinus Wilhelm Beijerinck, repeating the experiment, also recognized that there was an invisible cause and named the infectious agent,  “Tobacco mosaic virus.”  In the same year as Beijerinck’s report, two German scientists, purified a liquid containing ‘filterable viruses’ that caused foot and mouth disease in cattle (viruses were at one time called ‘filterable bacteria’, but eventually the term ‘filterable bacteria’ came to apply only to viruses, and was the words ‘filterable bacteria’ were dropped).  Walter Reed followed in 1901 with a filtrate responsible for yellow fever, and soon dozens of other disease causing viruses were found.
In 1935 , another American, Wendell M. Stanley, went back to the beginning and created pure crystals of tobacco mosaic virus from a filtered liquid solution.  He affirmed that these crystals could easily infect plants, and concluded that a virus was not a living organism, since it could be crystallize like salt and yet still remain infectious.  Subsequently, bacteriologists all over the world began filtering for viruses, and a new era of biology was born – Virology.
Historically, medical science has a baseline on the question of whether any virus is alive.  Originally, it was described as non-living, but is currently said to be an extremely complex molecule or extremely simple microorganism, and is usually referred to as a parasite having a cycle of life.  (The term “Killed” is applied to certain viral vaccines, thus implying an official conviction that viruses are alive.)  Commonly composed of either DNA or RNA cores with protein coverings, and having no inherent reproductive ability, viruses depend upon the host for replication.  They must utilize the nucleic acids of living cells.  They infect to reproduce their proteins (i.e., trick the host into producing them), which are then assembled into new viruses like cars on assembly line.  Theoretically, this is their only means of surviving, and infecting new cells or hosts.
Birth of Virology — a Miscarriage?
Underlying the birth of virology was the doctrine of monomorphism — that all microorganisms (herein called microforms) are fixed species, unchangeable; that each pathological type produces (usually), only one specific disease; that microforms never arise endogenously, i.e., have absolute origin within the host; and that blood and tissues are sterile under healthy conditions.  This last point warrants immediate comment.  Theoretically, under ideal health conditions, the blood might be sterile, though it has the inherent potential to develop morbid microforms, as discussed in my book, Sick and Tired.  Long and repeated observation of live blood in the phase contrast, darkfield microscope, however, shows that the blood can contain various microforms and otherwise asymptomatic host, or in a condition defined as normal or healthy in orthodox terms.  The forms are easily visible before other physical symptoms arise. (Since long and repeated observation has correlated their presence with other disease symptoms and their disappearance with the return of health, they serve as indicators of impending outward signs of disease).
Monomorphism was the cornerstone of developments in 20th-century medical research and treatments.  Refusal by the mainstream to examine fairly, much less except, the demonstrated fact of pleomorphism — that viruses and bacteria (and also yeast, fungi and mold) are evolutions from a small indestructible anatomical element, I referred to as the microzyma.  That microforms can rapidly change their form (evolve and “devolve”) in vivo, one becoming another dependant upon conditions in the inner terrain (environment); that blood and tissues are not necessarily sterile; and that there are no specific diseases, but only specific disease conditions — was the foundation of a latter-day “Galileo debate.”  It is so-called because those who wore the “robes” of scientific authority just like today, reprising the religious fanatics who punished the noted astronomer for his truth, would not be swayed from folly when presented with its contrary theory.  These truths began in earnest with Antoine Bechamp in the 19th-century (who also endured the indignation of a fanatical clergy).
In the early third of the 20th-century, the heated debate took place over ‘filterable bacteria’ versus ‘non-filterable’ bacteria.  This was a major battle concerning micromorphology (discussed briefly below). The orthodox view prevailed: bacterial forms were not small enough to pass, or did not have a smaller, earlier stage.  What passed through ‘bacteria proof’ filters was something else, i.e., viruses.  Standard medical textbooks, long made this filtering distinction between bacteria and viruses.  Subsequently, however, the cellular nature of many filterable forms originally thought to be viruses, such as some mycoplasmas, rickettsias, and various other groups, has been established.  In this writer’s opinion, with the victory of the monomorphic view, deeper understanding of infectious ‘disease’ was lost, setting the stage for cancer, degenerative symptoms, HIV. AIDS, Ebola, Hantavirus, Hep C, HPV, etc.
What You See?
A typical bacteria is about 1 micron in size.  Most filterable bacterial forms now called viruses range in size from .3 microns (300 millimicrons) to .01 microns (10 millimicrons) — particularly in the colloidal range  (.1 to .001 micron). Most of the larger viruses are a third to a quarter the size of the average bacteria.  And size is critical because .3 microns is the resolution limit of modern-day light microscopes.  Thus, as viruses were discovered (except for the very large ones, such as mumps), they required an electron microscope to be seen, especially given the the fact that Royal Rife’s microscope technology and career were destroyed by vested interests.  Unfortunately, electron microscopes and the process of chemical staining disorganize or damage all specimens, whereas Rife’s technology allowed life to proceed and thus evolve under its lens. As viruses became visible to advancing technology, the ratification was that the technology revealed, two minds infected with monomorphism, protein structures deemed foreign in the body.
A New Theory
Formulated by Antoine BeChamp in the 19th-century, the microzymian principal is the basis of the new theory about ‘viruses’.  Recently, this principle holds that in all living organisms are biologically indestructible anatomical elements, which BeChamp called microzymas.  They are independently living organized ferments, capable of producing enzymes and capable of evolving into more complex microforms such as bacteria, yeast or mold.  Bechamp’s thesis, is that disease is a condition of ones internal environment (terrain); that disease (and its symptoms) are “born of us and in us.”; and that disease is not produced by an attack of micro entities, but calls forth their endogenous evolution.
My studies and research suggests that the complexes, science calls viruses and retroviruses originate in the cell, as the microzymian as the principal suggests.  However, they are created in response to an alarming acidic situation (condition of disease) for the purpose of genetic repair.  They are repair proteins, evolved from anatomical elements (microzymas), not pathogenic  microorganisms.
It is known that normal cell activity includes genetic repair.  Both enzymes and proteins must be involved.  What is the mechanism?  Viruses are organized around DNA or RNA, not both.  Thus, they are quite probably intended to repair genetic molecules or other structures, and show up with disease symptoms, because the body needs them.  Since viruses require a living cell/host for reproduction, how do we know that the scenario is not set in motion, for a purpose by the cell (i.e., it’s microzymas), rather than being the result of invasion?  Because disease (disturbance of balance in the organism) is so prevalent, especially that which is not yet becoming indicated by common symptoms, repair proteins may be frequently or constantly present.  A toxified cell may easily suffer localized damage to the genome.  Since most observers are not even aware of the microzymian principal, much less understand or even consider it, and since monomorphism stresses invasion, these proteins complexes are regarded as foreign and disease is attributed to them.
Another note of interest is the size of viruses compared to the microzyma.  Viruses are considered to be some of the smallest biological particles and are frequently of colloidal size: e.g., hepatitis A, 27 nanometers (.027 microns); hepatitis B (.042 microns); polio virus (.03 microns); EBV (.042 microns); HIV (.080 to .12 microns); influenza (.08 to .12 microns); mumps (.15 to .30 microns); smallpox (.30 microns); and, according to BeChamp, the microzyma (.0005 microns).
In his book, ‘The Blood and its Third Anatomical Element’, Bechamp states: “the microzyma is at the beginning and at the end of all organization.  It is the fundamental anatomical element whereby the cellules, the tissues, the organs, the whole of the organism are constituted living . . . . in a state of health, the microzymas act harmoniously and our life is, in every meaning of the word, a regular fermentation.  In the condition of disease, the microzymas do not act harmoniously, the fermentation is disturbed, the microzymas have either change their function or are placed in an abnormal situation by some modification of the median.  The virus is either a self-ordered microzymian polymerization, or (less likely), a structure made by microzymas.  It is envelope in protein which is also composed of microzymas, and could well be thought of as an autonomous molecular tool box.
Along with doctors Glen Dettman and Archie Kalokerinos, I wonder, “whether Bechamp’s writing anticipated, in some respects, the discovery of RNA and DNA?”  Could the genetic structure be the construct, thus a tool, of the microzyma?  They quote a personal communication [1974] from a professor Bayev of the former USSR Academy of Sciences, who discusses his work showing the molecular self- restoration from its parts of pure transfer RNA from brewers yeast is possible.
In my own research I have found molecular restoration similar to that described by Bayev.  In my experiment , I used 10-year-old coagulated capillary blood from a woman with cancer.  With one drop of .9% of sodium chloride, the blood was restored to an appearance and level of activity characteristic of freshly drawn sample of blood.  In other words, the anatomical microzymas of the dry blood were restored to activity.  Even the white blood cells became active again.  One might eagerly asked for explanation of the reversal of polymers made during clotting.  It is unclear at this point how this reversal takes place, except to say that what can evolve apparently has the potential to devolve.  It is observable, however.  For example, I have seen, and recorded on video, rod microforms retro-grading without any visible decomposition from 10 microns in length to the vicinity of .1 micron.
This research supports the very important postulates that the cell is not the smallest living biological unit, as promulgated by conventional medical science.  In fact, a smaller biological unit is the imperishable micros I’m a, which is an organized, living been “of a special category without analog,” said BeChamp, who found them ready to become active in chalk deposits at least 11 million years old.
The Pleomorphic Cycle
I suggest a developmental cycle in vivo consisting of three macro stages: [1] a primitive stage comprising the repair proteins complexes; [2] an intermediate, or bacterial, stage including filterable forms such as the cell wall deficient forms described by Lida Mittman, PhD. [in Cell Wall Deficient Forms, Stealth pathogens]; and [3] a culmination stage consisting of yeast and fungal phases, and then mold, the and phase.  The usual course of development would be from microzyma to repair proteins, and then to bacterium, etc.  However, under certain conditions, such as, for example, it is highly likely that the microzymas can skip the primitive stage and become bacteria directly.  Although these transformations are as astounding as that of a larva to a butterfly, what is equally impressive under observation is in the rapidity with which they can take place — in minutes, even seconds, sometimes.  By the same token, when provoked by acidic conditions and the cycle proceeds to yeast, fungus and then mold, it may occur so rapidly that the bacterial stage, if that happens, has no time to be of any significance.
Thus, symptomgenic microforms can originate within the higher organisms without invasion, via a permutation of the endogenous microzymas when the situation calls for such change.  The situation is an imbalance referred to by Bechamp as a “modification of the median.”  Endogenous evolution is evident under the microscope when bacterial, yeast, and fungal forms are seen coming out of the red blood cells, which initially appear normal.
Biological Basis for the Pleomorphic Cycle
There is a common biological basis for the pleomorphic cycle and its increasing complexity of organization: more complex forms evolve inherently upon the death of an organism for the purpose of recycling its anatomical and chemical structures in the carbon cycle.  The process of rapid evolution [which is reversible] is an essential life process, which, beyond the repair stage, is necessary to return a dead organism to the earth.  The second and third stage microforms degenerate the body’s vital substances and tissues via putrefaction [bacteria] and fermentation [yeast and fungus].  Fermentation results in acidic waste products, which further breakdown tissue.  Disease symptoms, then, especially the degenerative type, are NOT produced by viruses, but manifest as chemical decomposition, or attempted recycling via fermentation and acidic toxins, but with ‘host’ survival processes still, operable.  Obviously, certain other factors may play important roles in producing symptoms, such as heavy-metal toxicity, or state of mind, for example.  Some of the body survival methods also produce symptoms commonly called dis-eases.  An example is eczema, and emergency expulsion of acidic toxins via the pores of the skin.
The aforementioned casual [alarming] situation, or modification of the median, is chronic tissue acidification [pH imbalance] and oxygen deprivation in the blood and tissues due to acidic forming foods, adverse lifestyle, emotional stress, and environmental stress.  This is not an oversimplification!  Acidification/hypoxia biochemically signals a dead host to the microzymas, while creating collapsed areas [dead zone’s] of the colloidal system in the intercellular fluid, and it is the primary physiological disease condition at which the symptoms commonly called specific diseases arise.
Thus, we distinguish between this disease condition and its consequent symptoms, which include both the morbidly evolved microzymas and the physiological science commonly thought of as specific diseases.  As they develop, microforms [bacteria, yeast, fungus and mold] are actually scavenging forms of the microzyma, developed when disease in the cell life requires tissue to be broken up.  These upper development forms are the ones easily visible in the blood before physical symptoms arise.  They disappear, [devolve] when the recycling task is complete, once again becoming microzymas of the earth and/or air.
Virus or Toxin/Acid?
Regarding the early period of virus isolation, a question is whether the unseen entities isolated in filtered fluids were accompanied by the waste products [mycotoxins] of fermentation by yeast and/or fungus of cellular elements, such as DNA.  If virus infiltrates are injected into a host to prove virulence, it is almost certain that easily filterable molecular toxins will be introduced as well.  Could Dr. Stanley’s “pure crystals of tobacco mosaic virus” have been crystallized acidic toxins?  If so, they would certainly be highly symptomgenic, as are exotoxins at the intermediate stage of the cycle, for example.  However, it is not proof of anything that you can create illness by poison injection, except proof of that tautological fact.
In my research utilizing darkfield and phase contrast microscopy, it is common to see acid crystallization’s in the blood.  It is normal for the body to use calcium or other mineral salts, and fats as well, to chelate the acidic waste products from the morbid fermentation of body proteins, fats and sugars.  Such crystal deposits are found in cancer tissue as well.  A malignant tumor removed from the breasts of one of my research clients was found to have numerous calcium deposits attached to it.  It is an attempt to render inactive acidic substances that make our inner streams healthy, poison our cells, and coagulated colloidal systems in blood and intercellular fluid.
The term “virus” is the Latin word for poison, and gives us insight into the immediate cause of disease symptoms — poison is: exotoxins and mycotoxins, and a toxin, exotoxins, and toxins from environmental sources, [many of which are primary or secondary mycotoxins.].  Orthodox medicine is well aware that it is bacterial toxins more than the bacteria them self.  [They feed in-house], that caused the symptoms referred to as infectious disease.  Little if any emphasis is placed on this fine, but important distinction.  Always, the germ is emphasized.  There is little too, no awareness [or knowledge that], either, of the same role played by acidic toxins of the culminate microforms of the pleomorphic cycle.  Their action and the body’s response to them are frequently ascribe to viruses, which do not produce toxins because they are the toxin or acid, but are said to wreck havoc by a number of other means.  However, if they participate in symptom at Genesis in a host it is because they are stimulated to evolve into more complex, toxic genetic forms.  Somewhat less likely is the possibility that they cause damage as a result of erroneous construction or function, for one reason or another — missing mineral nutrients leading to alkaline mineral deficiencies, for example.
Misconception Breeds Contempt
In addition to chemical toxicity, however, what is the impact of the fear [emotional toxicity] that the word “virus” brings to mind and heart?  It has been said that fear it is the most deadly of disease conditions.  If the “disease” kills one person, the fear of it may kill 20.  General prejudice concerning the danger of viruses is fundamental biological error based on Louis Pasteur’s germ theory, and is itself a perpetrator of auto-suggested illness.  For example, in Africa doctors attribute some AIDS sickness to “voodoo death” syndrome, the term for illnesses induced psychologically.  According to one nurse, “we had people who were symptomatically AIDS patients.  They were dying of AIDS, but when they were tested and found out they were negative they suddenly rebounded and are now perfectly healthy.”  Ironically, if the germ theory were found on facts, it would be correct to fear viruses, except there would be few, if any, humans living to discuss the issues.  These so-called pathogenic entities are to researchers, medical practitioners and the press what criminals are to detectives — the focus and justification of their existence.
The Encyclopedia Britannica has this to say about bacteria, which relates also to viruses:
“The common idea of bacteria in the minds of most people is that of the hidden and sinister scourge lying in wait for mankind.  This popular conception is born of the fact that attention was first focused upon bacteria through the discovery, some seven years ago, of the relationship of bacteria to disease in man, and that in its infancy, the study of bacteriology was a branch of medical science.  Relatively few people assigned to bacteria, the important position in the world of living things that they rightly occupied, for it is only a few of the bacteria known today that have developed in such a way that they can live in the human body, and for everyone of this kind, there are scores of others which are perfectly harmless and far from being regarded as the enemies of mankind, must be numbered among his best friends.
It is in fact, no exaggeration to say that upon the activities of bacteria.  The very existence of man depends; indeed, without bacteria there could be no other living thing in the world; for every animal and plant owes its existence to the fertility of the soil, and this in turn depends upon the activity of the microorganisms which inhabit the soil in almost inconceivable numbers.  It Is one of the main objects of this article to show how true is this statement; there will be found in it only passing reference to the organisms which produce disease in man and animals — for information on these see Pathology and Immunity.  [Encyclopedia Britannica, 14th ed., Volume 2, page 899].
The general message of the foregoing article applies even more aptly to viruses in the sense that much fear has been bred and cultivated around them, although they never produce disease symptoms, whereas the acid waste products of bacteria, yeast, fungus and mold do.  The writer of the above understands bacteria, with the exceptions that symptomgenic bacteria found in man and animals do not produce disease.  [Only secondary symptoms], that their precursors are endogenous to higher organisms, and they have not “developed in such a way that they can live in the human body.”  If anything, the reverse is true.  According to one theory of microbiology, microforms have colonized over eons to become higher organisms.  In one sense, then, the human body has developed as a specialized environment for them.
An important dimension of the bacterial dependence of higher life forms is the floral population in the human digestive tract.  Literally, these “foreign species” keep us alive.  Most bacteria have the same underlying function, whether found in the soil, sewage, in the human digestive tract, or elsewhere in nature: they are an essential part of the life processes of hire organisms.  They will not or cannot attack healthy cells or tissues, but certain ones will recycle sick or dead tissue in much the same way insect pests are drawn to weaker plants.  As Bechamp said, “nothing is the prey of death; all things are the prey of life.”
Following in the wake of misconceptions arising from the fundamental biological error known as the germ theory of disease, defying infiltrates of disease tissue as a newly discovered infectious microforms was the birth of a major corollary error in bio science.
Viral Behavior Reconsidered
Listed below are ways of viruses are said to disrupt or destroy host cells.  According to orthodox medical science and the germ theory advocates.  Following each in its italics is a different interpretation following from microzymian principle:
1.  Viral proteins insert into the host cells , plasma membrane and directly damage its integrity , to promote cell fusion [HIV, measles, and herpes viruses.].
Proteins are attempting to repair membrane damage, or enter cells to repair other proteins.  There is the question as to whether viruses on cell walls are coming or going.  In both cases, it would be a matter of whether or not a cell has been disturbed by excess fermentation and acidity.  But in the former case, the cell would be dysfunctional before attachment occurs, thus requiring the repair complex.  Another possibility, perhaps remote, is that dysfunctional receptors on cells are in need of repair, or they are covered by these complexes to inactivate malfunction of the cells.  Positive electrical charges in a compromised acidic terrain, primarily on acidic molecules from fermentation’s, discharge cell membranes and act as mortar to stick cells together causing rouleau and clotting.
2.  Viruses inhibit a host cell DNA, RNA, or protein synthesis.  For example, polio virus inactivates cap-binding protein, which is essential for protein synthesis, directed by capped host cell mRNA’s, while allowing protein synthesis from uncapped polio virus in mRNA’s.
Protein inactivation is probably being done by fermentation or by acidic toxins from fermentation, while “poliovirus” is produced in the cell to reverse the damage.
3.  Viruses replicate efficiently and lyse host cells, e.g., liver cells by yellow fever, and neurons by poliovirus.
Highly unlikely.  The lysing is more likely caused by acidic mycotoxicosis, or by free radicals released in response to mycotoxic stress, or from other sources [I lysine radiation, for example].  Repair particles are residual after cell wall disruption.
4.  Slow-virus infections [e.g., sub acute sclerosing panencephalitis caused by the measles virus] culminate in severe progressive disease is after a long latency period.
How is this demonstrated?  Perhaps “latency” is a period of unsuccessful or attempted repair that eventually falters.  Symptomology naturally appears in the weakest parts of the body.  Excess acidity is always a systemic problem that localizes, just as cancer is a systemic acidic condition that localizes, even though it its symtogenic influence may later spread.
5.  Viral antigen proteins on the surface of the host cells are recognized by the immune system, and the host lymphocytes attack, the virus infected cells [e.g., liver cells infected with hepatitis B].
Liver cells are damaged beyond repair by exotoxins and mycotoxicosis, and the immune system, our elaborate janitorial service, is cleaning out the garbage.  Perhaps the repair protein antigen is expressed to signal any in response [because the cell is beyond repair], which is one explanation for why there are antibodies to these proteins.
6.  Viruses damage cells involved in the host anti-microbial defense, leading to secondary infections.
The function of immune cells are damaged by bacterial or fungal waste products/acidic and/or overworked by toxic acidic overload, preventing proper cleanup and elimination of disharmonious, symptomgenic elements.
7.  Viral killing the one cell type causes the death of other cells that depend on them, e.g., degeneration of muscle cells enervated by the attack of poliovirus on motor neurons.
Once again, a misinterpretation and lack of understanding that is not viral microforms that damage neurons.  Acidic toxins from bacteria, yeast, fungus and mold — as well as the ferments of glucose, uric acid from proteins, hormones and acetic acids from fats — produce, or influence the body to produce, dis-ease  or inflammatory symptoms.  Not recognizing “virus,” for what it is, observers attribute dis-ease or disease to it.
8.  Host cell responses to viruses include metabolic derangement and transformations resulting in neoplastic changes.
Metabolic derangement has occurred prior to the appearance of repair proteins, due to toxic overload in the cell.  It is more likely that the proteins attempt to prevent cell transformation, and that cancerous development is cell conversion from primarily oxidative to wholly fermentation of metabolism, mediated by yeast, fungus and mold.
9.  According to orthodox theory, viruses enter a host cell and replicate at the host’s expense.  Replication is accomplished using enzymes, which are distinct for each virus family.  For example, RNA polymerase is used by negative stranded RNA viruses degenerates positive stranded mRNA, or as reverse transcriptase is used by retroviruses to generate DNA from their RNA template and to integrate that DNA into the host genome.
It is normal for repair proteins to generate enzymes or acidic waste products as they do their work of repair.
10.  one reason suggested for viral tropism [the tendency to infect some cells, but not others] is the presence or absence of host cell receptors that allow the virus to attach.  It is said, for example, that HIV binds to the proteins [CD4] involved with antigen presentation on a helper.  The lymphocytes, that Epstein-Barr virus binds to the complement receptor [CD2] on macrophages, that rabies virus binds to the acetylcholine receptor on neurons, and that rhino viruses bind to the adhesion proteins [ICAM-1] on mucosal cells.
See answer to number 1 above.
Theoretically, once attach, the entire virion, or a portion containing the genome and essential polymerases, penetrates into the cell saddle plasma in one of three ways: [one] translocation of the entire virus across the plasma membrane; [two] receptor mediated endocytosis of the virus and fusion with endosomal membranes; or , [three] fusion of the viral envelope with the cell membrane.  Theory suggests that within the cell the virus uncoats, separating its genome from its structional components and losing its infectivity before replication.  In either the nucleus or the cytoplasma, newly synthesize viral genomes and capsid proteins are assembled into progeny virions, which may then bud to the plasma membrane.  Unencapsulated viruses may be released also, directly through the membrane.
It is interesting, however, that viruses can somehow choose the “infection.”  To be aborted, latent or persistent, meaning respectively: [one] viral infections with incomplete replication cycles; [two] persisting in the cryptic state, like herpes zoster within a dorsal root ganglion, which suddenly becomes active to produce shingles; [three continuously synthesized virions, with or without altered cell function [e.g., hepatitis B].  These three ideas, especially latency, have arisen as feeble excuses for the untenable virus theory.
11.  In order for viruses to reproduce, they must complete the following four steps:
a] Adsorption and penetration of the cell.  The viral particle binds to the host cell membrane.  This is unusually a specific interaction in which a viral encoded protein on the capsid or a glycoprotein embedded in the virion envelope binds to a host cell membrane receptor and is then internalized.  This internalization occurs by endocytosis or by fusion of the virion envelope with the host cell membrane.
This is the mechanism whereby the viral particle enters the cell for the purposes of carrying out repairs to the damaged DNA or RNA.
b) Uncoating of the virus, so that the nucleic acid can be released from the capsid into the nucleus or cytoplasm.
Repair work may require uncoating.  An uncoated “virus” in the saddle plasma, may have, from the nucleus and not yet have a code, as in the case of hepatitis B , according to medical science.  A coat is then created to protect the nucleic acid, to make a communicative or response to protein complex, or to allow exiting the cell for remote function or for neutralization and recycling by the immune system.
c) Synthesis and assembly of viral products, as well as in addition of the host cell’s own DNA, RNA and protein synthesis.
Protein complex is produced in response to an alarming acidic situation — fermentation and mycotoxic stress — are capable of self-reported replication.  As suggested by Bechamp, the microzyma is specific for each organ, therefore specific repair proteins will be needed for specific cells that make a specific organ that are being disturbed by dietary and/or metabolic acidic waste products.  There is the question of why the great numbers in some cases.  One possibility is simply over reaction; for example, fever can be extreme.  Why?  To remove dietary, metabolic acids or acids from bacteria, yeast, fungus and/or mold.
d) And finally, release of virions from the host cell either by budding or lysis.
[1] Complexes leave the cell for remote function or to be neutralize; [2] repairs have failed, and complexes are released prior to or during the breakdown of the cell by acidic toxins or the immune system.
Further Considerations
Virologists referred to certain microforms as passenger viruses, which are present in asymptomatic situations, riding on their host genetic molecule like a passenger.  To the conventional mind searching for new diseases or for viral cause of unexplained ones, they are most interesting, because the status virologist in the scientific community depends upon the pathogenic potential of the viruses they study.  Due to their location, passenger viruses are thought to have much disease potential, thus their true function goes unnoticed.  These colloidal passengers are the silent majority of animal and human intranuclear proteins essential for genetic repair.
Kalokerinos and Dettman quote Dr. Fred Klenner regarding the changeability of viruses, “I am of the opinion that virus units have the potential of going from one type to another by altering their protein coat.  We see chickenpox at Thanksgiving, mumps at Christmas, read measles in the spring, and polio and Coxsackie in the summer.”  Seasonal appearance of different forms may be mediated by variations of imbalance in the biological terrain or nutritive median due to the fermentation of dietary excesses such as sugar and animal proteins that accompany holidays and seasons, calling for different repair proteins.  For example, outbreaks of polio have been associated with sugar consumption in summer.  Various psychoemotional stresses correspond to the seasons as well.”
Supporting the general idea of dietary culpability is a statement published by the great English physician, Sir Robert McCarrison in 1936: “obsessed with the invisible microbe, virus, protozoa as all-important excite tens of disease, subservient to lavatory methods of diagnosis, hidebound by our system of nomenclature, we have to forget the most fundamental of all rules for the physician, but the right kind of food [nutrition] is the most important single factor in the promotion of health and the rhonchi to food.  The most important single factor in the promotion of disease.”
Six years before BeChamp identified the microzyma as a ferment and, with his devoted associate, Professor Estor, began a 13 year odyssey of research into its nature. Florence Nightingale published a statement about the germ theory,  In ‘Notes on Nursing’, first addition, 1860, she said of infection:
“Diseases are not individuals arranged in classes, like cats and dogs, but conditions growing out of one another.
Is it not living in a continual mistake to look upon diseases, as we do now, as separate entities, which must exist, like cats and dogs, instead of looking upon them as conditions, like a dirty and a clean condition, and just as much under our own control; or rather, as the reactions of kindly nature against the conditions in which we have placed ourselves?
I was brought out . . . . distinctly to believe that smallpox, for instance, was a thing of which there was once a first specimen in the world, which went on propagating itself in a perpetual chain of dissent, just as much as that there was a first dog, [or a first pair of dogs], and that smallpox would not begin itself anymore than a new dog would begin without there having been a parent dog.
Since then, I have seen it with my eyes and smelt it with my nose smallpox growing up in the first specimens, ear in close rooms or in overcrowded wards, where it could not by any possibility have been ‘caught’,  but must have begun.  Nay, more, I have seen diseases begin, grow up, and pass into one another . . . . I have seen, for instance, with a little overcrowding, continued fever grow up; and with a little more, typhoid fever; and when little more, typhus, and all in the same ward or hut.
Would it not be far better, truer, and more practical, if we looked upon disease in this light?  For diseases, as all experience shows, are adjectives, not noun- substantives.”
That is, symptoms [called diseases] are described first of the situation.
I find legitimate BeChamp’s conclusion that what are called germs of the air are fundamentally microzyma’s of beings, which are being consumed by the recycling process, i.e., some kind of vegetative digestion — putrefaction or fermentation.  In short, there are no pre-existing disease germ species.  The principals of microbial medicine constitute a fundamental biological ERROR!!!!!!  As BeChamp said, “the microbial doctrine is the greatest scientific silliness of this age.”  This is not to say there is no transmission, only that invasion is not necessary for symptogenesis, nor is it the primary mechanism for illness.  It is to say that for transmission to take place, susceptibility in the form of a compromised terrain must pre-exist in the receiver, who was then likely to be ill anyway.  With the exception of the immune component in the mucosal barrier, primary host “resistance” is a function of terrain condition rather than immunity per se.
Phantom Viruses
 
Hepatitis
Hepatitis can be a painful symptom that has yielded profitable virus hunting opportunities in recent years.  Although there are several categories of this disorder, three main varieties of what is called “acute viral hepatitis” exist: Type A [formally, ‘Infectious hepatitis’], Type B [formally ‘Serum hepatitis’], and hepatitis Type C (formally ‘non A, non-B’].  The corresponding viruses are HIV, HBV, and the non-A, non-B ‘group’, now called C. Type A is said to be caused by an RNA virus, spread primarily by fecal contamination of water and food, with blood and secretions also possibly being infectious [but it is due to the acidic toxins associated with unsanitary conditions].  Hepatitis B, discovered in the sixties, is said to be caused by a DNA virus, which replicates in the hepatocyte nucleus and receives its surface coat in the cytoplasma.  It is said to be transmitted by transfused blood or blood products, or via common use of needles by intravenous drug users [but it is due primarily to over-acidification from the drugs, especially heroine.  The exchange of body fluids into the blood, whether by sterilize needles, abusive sexual activity, eccentric sexual activity, etc. can also play a role overtime, because of repeated immune stress caused by foreign proteins].  Third World babies with poor nutrition and unsanitary conditions around the time of birth are also susceptible.
The third type of hepatitis, discovered in the seventies, is found among drug users and alcoholics, and accounts for 80 to 90% of hepatitis caused by blood transfusion.  It is thus akin to B type and was at first thought by scientists to be hepatitis B until thorough testing a subject revealed no virus B nor A, for that matter.  It was thus called “non-A, non-B” hepatitis and thought to be at least two viruses and perhaps more.
In 1987 scientists believed they found a single virus causing the third type, what is known today as the hepatitis C virus.  However, what they identified was an antibody, they associated with a virus.  Now, just as with HIV, they could test patients for antibodies against an elusive or invisible phantom virus.  With this new observation, however, new paradoxes confronted the viral hypothesis.  Huge numbers of people testing positive for the Phantom C virus never developed any symptoms.  Hepatitis C is truly the result of an over-acidification or toxification of the largest filter organ in the body by such substances as lactic acid, acetylaldehyde and ethanol alcohol — not the disease of a pathological phantom virus.  It is interesting to note also that all these hepatitis viruses have incubation periods of two to 25 weeks, violating Farr’s law, [see below], yet are not classified as slow viruses.  Also, the point at which a “natural invasion” takes place, as opposed to a highly artificial in objective one, and thus, how true incubation periods are determined, is another interesting question.  Bottom-line there is no Hepatitis C virus.
Hantavirus
A recent example of unwarranted panic in American bio medicine was the eminent hantavirus of 1994.  Presumably, it had jumped species, from mouse to man [the American Navajo Indians].  However, after supposedly killing a number of people, this phantom virus apparently made peace with the Indians and retired to its mouse reservoir.  The virus failed to materialize.  A front-page article in the San Francisco Chronicle reported that CDC “epidemiologist across the nation are carefully monitoring the deer mouse population and the level of virus within it.”  But all that was left to discover of the former.  “Navajo flu” by the CDC epidemiologist [shown in their space suits] were healthy mice in the mountains.  The Navajo flu is nothing new to the Native Americans and is most likely tied to sanitation, nutrition and lifestyle.
Ebola
In May 1995 , the CDC announced the new, threatening Ebola virus.  The deadly killer virus was expected to leave its hidden reservoir in the rain forest of Africa to claim Europe and the United States.  An article in Time magazine was peppered with men in space suits and color electron micrographs of the virus  [even though electron microscopes cannot take color pictures and the pictures were of parasites].  A CDC virologist suggested the virus could leave the rain forest a if “we get a virus that is both deadly to man and transmitted in the air.”  We are thus asked to fear the false image of virus somehow being launched into the air, perhaps by injection from a host, and then floating on a killer breeze to other lands.  A more imaginable scenario was suggested by European epidemiologist who heads the United Nations AIDS program.  Echoing the the CDC’s alarm, he stated, “it’s theoretically feasible.  Then infected person from Kuwait could go to Tunisia, get on a plane to New York, fall ill, and present transmission risk there.”  But within a month, the virus had disappeared in Africa, and not a single Ebola case was reported in the United States or Europe.
The World Health Organization announced on December 19, 1995 that the Ebola virus epidemic that killed 245 people in West Africa was over.  All tests on any remaining suspected cases were negative.  A somewhat unsettling revelation was that every Ebola outbreak in Africa, “is associated to have spread to public hospitals.”  As it turned out, it was associated with reused hypodermic needles in these hospitals.  Just like hantavirus, Ebola vanished, never to be heard from again, until NOW!  Most interesting is that this so-called epidemic, as epidemics will, stopped without vaccines or other drugs.  Consider the impact such stories have made upon our minds and on the way we view and understand germs.  What’s next in the virodrama, the Andromeda strain?  NO!  Here we go again with the same old phantom viral story!
There is one insidious possibility that must be mentioned in passing.  Some mysterious outbreaks of the past have shown years later to have been man-made.  In some cases, government agency have used the public to test releases of organisms and weak biochemical acidic toxins in order to verify, through medical reports, expectations of bio-warfare activity.  These incidents and the whole story of such behavior is well documented in the book, all higher forms of killing by Robert Harris and Jeremy Paxman [Hill and Wang, 1982].  In this scenario, the cause of such an incident would be constructed officially, or left as a mystery, in order to draw attention away from the truth.
Resources:
  1. To read Part 2 and Part 3 and for all references for this article read Sick and Tired by Dr. Robert O. Young – http://www.phoreveryoung.com, http://www.phmiracle.com or http://www.phmiraclebooks.com

The Top 21 Biggest Medical Lies – Including The Flu Virus Lie!

The Top 21 Biggest Health, Nutritional and Medical Lies

The following list includes the biggest health, nutritional, and medical lies, deceit, deceptions and inventions that we have been told by a doctor, a nurse, a scientist, a teacher, a nutritionist, a health guru, a Pharmaceutical Company, the American Medical Association, the American Cancer Society, the Center of Disease Control and/or the World Health Organization, just to name a few.

1) The Mexican Swine Flu Virus is a potential pandemic and can kill you.

This is a scientific illusion. Viruses do not kill, acids kill. All viruses are nothing more than dietary and/or metabolic acid. The word virus in Latin means poison or acid. All flu’s or acids by definition effect only the gastrointestinal tract due to acidic foods and drinks ingested – not viruses. So the Mexican Swine Flu Virus that has been reported by the CDC to have killed over 1000 Mexicans is the result of an excess of gastrointestinal acid from the ingestion of acidic foods and drinks that have not been properly buffered by the stomach with alkaline salts or eliminated through the four channels of elimination – lungs, bowels, bladder and/or skin. For these unfortunate Mexicans or others in the US or around the world that have died, the cause of death was due to an excess of acidic foods and drinks, including Tequila, beer, beans, rice, corn, peanuts, yeast, soy sauce, high sugar fruit, processed sugar, artificial sugar, dairy products, chicken, turkey, beef and of course the biggest acid of all – SWINE. That’s right, the acids from PORK can kill. So 1000 Mexicans did not die from a pHantom Mexican Swine Flu Virus but they died from a dis-ease I call, “I Ate and Drank TOO Much Acidic Crap Disease” or “I Received An Acidic Flu Vaccine.” The simple solution for protecting you from an excess of gastrointestinal acid from an acidic diet and lifestyle that can and does kill is to increase your alkaline buffering mineral salts. All flu’s or acid outbreaks can be prevented and reversed with sodium, magnesium, potassium and calcium bicarbonate. YES, it is that simple! You can prevent gastrointestinal acidosis that can lead to stomach flu, vomiting, dehydration, diarrhea, constipation, and even death. No need to fear a pandemic, just the acidic foods and drinks you are ingesting and more specifically an acidic toxic swine flu vaccine. You can protect yourself and your family with the pH Miracle Lifestyle and Diet I call, “Young Living.” That is why I created the products pHour Salts, puripHy salts, pHlavor salts and pHlush salts. To learn more about these Young pHorever acid protecting products go to:

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2) Pandemics are caused by air-born viruses that infect the human or animal body causing sickness, disease and death.

This line of logic is responsible for more pain, suffering and death than any other theory. It is based upon the Pasteurian germ theory that germs or pathogens cause disease. Germs DO NOT CAUSE DISEASE – ACIDIC LIFESTYLES, DIETS, DRUGS AND VACCINES CAUSE DISEASE. Dis-ease and so-called disease is NOT something you get it is something you do. HIV, HPV, EBOLA, HUNTA, SARS, AVIAN FLU, AND THE SWINE FLU ARE ALL PHANTOM VIRUSES. THEY DO NOT EXIST. What exists is acidic lifestyles, acidic diets, acidic drugs and acidic vaccines. If you put alcohol into your body you can get drunk and sick. If you put tobacco smoke into your lungs you can get sick and cancerous. If you elect to have an acidic vaccine you can get sick and die! Not from some so-called virus but from the acidic elements of the alcohol, tea, coffee, meat, cheese, eggs, tobacco, anti-biotic or anti-life vaccines, etc. The key to health, energy and vitality is to maintain the alkaline design of your body. To poison your body with a vaccine will not increase your health, energy or vitality but only prove that you can poison yourself and hopefully live through it. True immunity comes from protecting the alkaline design of the body. ALL pandemics are caused by MAN and their acidic choices not some phantom virus!

The following is an historic precedent – The year was 1921.

America was entering a decade of robust prosperity. Later called “The Roaring Twenties”, it was a time of unparalleled economic expansion. Debt money from Wall Street banks was plentiful and easy to obtain. The “Great War” was over.America was flexing her industrial muscles. Factories were being built and expanded in every major city. Automobiles began rolling off Detroit assembly lines in record numbers. The stock market began making millionaires. 
People were HEALTHY and HAPPY largely because the dreaded “world mystery disease” (which decades later became known as the “1918 Flu Pandemic”) had disappeared. Two entire years had passed with no dreaded “mystery deaths” being reported. America had cause to celebrate, and celebrate they did!
As a matter of fact, the American Public in general was so optimistic and HAPPY in 1921, that relatively few people were unhealthy as well. For the first time in decades, hospital beds were empty. The fledgling American Medical Association, formed by John D. Rockefeller just a few years earlier, was worried. Business was sagging.Profits from vaccines and drugs were spiraling. Something had to be done, and done immediately. False, faux epidemics of smallpox were created to solve the problem, and keep the Medical Mafia’s cash registers ringing.

We know this dastardly plan actually happened, thanks to a citizen’s WATCHDOG GROUP in Kansas City, Missouri named “The Advertiser’s Protective Bureau”, who filed, and successfully prosecuted criminal charges against the Missouri state chapter of the AMA the Jackson Medical Society. The ‘Protective Bureau’s” official report of this cold-blooded plot reads as follows:
“In the Fall of 1921, the health of the city was unusually good, but slow for the doctors. So the Jackson Medical Society met and resolved to make an epidemic in the city. According to the minutes of this meeting: ‘MOTION WAS MADE AND SECONDED, THAT A RECOMMENDATION BE MADE BY THE COMMITTEE, TO THE BOARD OF HEALTH, THAT AN EPIDEMIC OF SMALLPOX BE DECLARED IN THE CITY. (Investigation later revealed that there was NO SIGN OF AN EPIDEMIC at the time, in the city, or anywhere in the state or region!)
‘It was moved and seconded that a day be set aside, termed VACCINATION DAY, on which physicians would be stationed at ALL SCHOOLS, clinics, public buildings and hospitals to vaccinate “free of charge”. (Vaccinations are never “free”. The taxpayers are always forced to pay for every one of the “free” vaccines.)
“IT IS FURTHER RECOMMENDED THAT WIDE PUBLICITY BE GIVEN, STATING THAT VACCINATION IS A PREVENTIVE OF SMALLPOX, AND URGING THE ABSOLUTE NECESSITY OF VACCINATION FOR EVERY MAN, WOMAN, AND CHILD IN THE CITY.”
The Protective Bureau proved in court that there WAS NO EPIDEMIC before the vaccinations!! The court records show that the Medical Society manufactured vast amounts of posters, fliers, newspaper stories and ads featuring horrific and lurid pictures of diseased children covered with massive smallpox sores and open wounds. Some pictures actually showed children’s corpses covered with the same ugly sores. 
The PANIC-DRIVEN message was clear — VACCINATE EVERYONE, or face a deadly public disease. There was a “sweeping epidemic” in the city; the disease was “highly contagious” and would “strike anyone who was not vaccinated” was the bill of goods sold! (Does this sound at all familiar today 88 years later??)
The Medical Mafia’s propaganda blitz was successful, and over a million previously healthy and happy American citizens were hypnotized and terrorized into placing the vaccine toxins into their bloodstreams. All public school children in the region were vaccinated while at school! Parents who dared question the vaccination of their children were ostracized and publicly vilified.
THE COURT RECORD ON THIS CASE IS VERY CLEAR. In the weeks and months following the “mass vaccinations” the area’s hospital beds were filled to over-flowing with VACCINE-INDUCED SMALLPOX CASES!
Tens of thousands of people became ill, and many hundreds of innocents died, and many more were permanently crippled! Of course, THE NEWSPAPERS THEN TRUMPETED HOW WISE THE MEDICAL ESTABLISHMENT WAS TO PROMOTE THE VACCINES stating how much worse the death toll would have been without the vaccination campaign!! Untold MILLIONS OF DOLLARS of profit was generated by this massive “medical” fraud.
Thanks to the ADVERTISER’S PROTECTIVE BUREAU, however; the massive fraud was exposed and criminally prosecuted to a successful conviction. During the trial, three amazing facts were proven beyond any “reasonable doubt”.
Fact 1: The poster and advertising pictures showing the diseased and dying children used so successfully by the “doctors”, WERE NOT EVEN CASES OF LOCAL SMALLPOX CASES AS THEY WERE BILLED TO BE! The Protective Bureau documented that they were pictures of ENGLISH CHILDREN who were victims of “court-proven” cases of SMALLPOX VACCINE POISONING!! One of the pictures was of a 5-week-old baby named Mona Stevenson, of Humphrey Street, Burnley, England. A previously healthy and happy baby, Little Mona had been vaccinated for smallpox at 5 weeks of age. Four weeks later, her pox-ridden little body was placed in a tiny coffin and buried. The horrific photos of Little Mona and others in England had previously been published in British newspapers where details of the resulting CRIMINAL TRIALS were also given. The full details of the trials, as well as the pictures, were also included in a comprehensively large medical boot titled “THE HISTORY AND PATHOLOGY OF VACCINATION” by Edgar M Crookshank, MD professor of Bacteriology at the ultra-elite Kings College, London England.
Fact 2: Vaccines containing LIVE ACIDIC (so-called) VIRUSES/TOXINS, weakened (i.e. attenuated) or otherwise universally causes more diseases than the vaccine ever could prevent.
Fact 3: Vaccine-Induced-Disease (VID) is an extremely effective socio-economic tool. It has the potential to generate BILLIONS OF DOLLARS OF WINDFALL PROFITS, while permanently changing the social structures of large groups of people.
While the Protective Bureau won the criminal court case the American people lost. The case should have made front-page headlines around the nation, showing the Modus Operandi of certain corrupt “medical practitioners”. How, by means of fraud, treachery, and trickery, they made millions of dollars in windfall profits while thousands of innocent, trusting, and naive Americans suffered and died. The entire sordid affair, with all its damning details, was kept out of the American Press. John D. Rockefeller’s AMA, with its millions of dollars of influence made sure of that!Amazingly, even though thousands of people had died or become crippled by this managed manslaughter, the doctors involved were only given a light penalty in the form of a token fine. The medical establishment as a whole was not upset in the least by the exposure and has continued on unabated perpetuating the same crimes against humanity creating acidic vaccine-induced-dis-eases while fleecing the people continually until this present day.
It is a proven (albeit little-known) fact, EPIDEMIC/PANDEMIC MANUFACTURING IS STANDARD PRACTICE with the world-wide “Medical Mafia” circles. In order to maximize profits and re-shape geographical regions, they often manufacture a false-flag “emergency”. If there is an outbreak of mild seasonal dis-esase from over-acidic choices, they call it an influenza pandemic, give it a fancy new name, and then actually CREATE THE PANDEMIC by means of mass vaccinations using ATTENUATED, or PURE ACID!! Remember the shocking words of the AMA’s Dr. Simon Louis Katzoff who said: ” DOCTORS LIVE BY DISEASE, SO THE PUBLIC CAN EXPECT THE SUPPLY OF DISEASE TO MEET THE DEMANDS OF THE MEDICAL PROFESSION.”

Those who cannot remember the past are condemned to repeat it.George Santayana

Those who are ignorant of the past, cannot be expected to remember it.True Ott, PhD, ND

 3) The Flu vaccine will protect you from the flu virus.

This is a falsehood. There is no such thing as a flu virus and therefore there is no need for a poisonous acidic flu vaccine made with chicken embryos, formaldehyde, mercury, detergent, and alcohol. The flu is the body in preservation mode increasing body temperature to activate the lymphatic system to remove excess dietary and/or metabolic acids in the tissues via respiration, perspiration, defecation and urination. The key to reversing the symptoms of the Flu is hydration with alkaline fluids and sweating with infrared sauna or exercise.

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http://www.phmiracleliving.com/p-189-ph-miracle-dry-heat-sauna-model-1000.aspx
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4) The 1976 “Swine Flu” Fiasco and Fraud is Being Perpetrated Today.

A solitary soldier at Ft. Dix collapses and dies following a reaction to an “experimental” acidic vaccine while completing an intense physical “forced march” exercise at Ft. Dix. Immediately, the CDC swings into action, declaring a nationwide SWINE FLU PANDEMIC is pending. Providentially, of course, the CDC just happens to have 200+MILLION DOSES of Swine Flu vaccine already stockpiled, prepared with ATTENUATED (live, yet weakened) so-called viruses and experimental acidic ADJUVANTS.

President Gerald Ford, (with proven ties to Big Pharma and Nixon’s covert viral or acid weapons labs also a key member of the “Warren Commission’s” obfuscation of the JFK murder) rolls up his sleeves on national TV and dutifully takes the vaccine. 40 million acidic vaccines are given to naive American human guinea pigs. A rash of auto-immune disorders (Guillan-Barre Syndrome GBS, and lupus) as well as a large number of deaths is immediately attributed to the acidic vaccine, and the mass vaccination campaign is halted. (What happened to the other 140 million vaccines, one may ask?) In 1979, the television news magazine 60 Minutes did a documentary investigation on this travesty-for-money scandal. Against all odds and the threats of Big Pharma, the OBJECTIVELY FAIR 60 Minutes program aired ONE TIME. There was no follow-up story, No criminal indictments were ever issued. There was no MASS-MURDER-FOR-HIRE trial. As a result, America has largely forgotten the 1976 SWINE FLU SCANDAL! Click here for “http://www.youtube.com/watch?v=5lcJt4jX1Vo” Part I of the 60 Minutes story; and “http://www.youtube.com/watch?v=r4c9Is1T3z4”
Part II.

The definition for insanity is doing the same thing over and over again and expecting a different result. All acids kill and vaccines are all made from acid.

5) Taking antibiotics will kill bacteria.

This is medical subterfuge and distortion as even the medical community realizes that antibiotics don’t do what they are supposed to do. We say with alarm that disease is becoming resistant to antibiotics. They are not “resistant” because they have never been operative or effective. Antibiotics are the acidic waste products of fermentation. To make an antibiotic, you need a yeast or mold and some sugar for the yeast or mold to ferment. The bi-product of the yeast or mold fermenting the sugar is the acidic antibiotic. The acids from antibiotics DO NOT KILL BACTERIA. They only force the bacteria to change. Into what does bacteria change? Into yeast and mold. That is why when you take antibiotics you end up with a yeast infection! That’s the antibiotic causing the bacteria to change from one form to another. I call this process of change “biological transformation” and the reason why you should NEVER take antibiotics. Try the COWS Plan. It is safer and more effective.

http://www.phmiracleliving.com/p-383-young-phorever-cows-starter-pack.aspx

6) The stomach should be acidic and contains hydrochloric acid or HCL to digest food.

This is one of the biggest scientific misconceptions ever. First, the stomach is NOT and organ of digestion. Most so-called digestion starts in the mouth. That’s why your mom said to chew your food. The stomach is an organ that alkalizes the food and liquids that you eat. The stomach cells, called the cover cells, secrete sodium bicarbonate onto the ingested food and drink to alkalize the food, not to digest the food. For every molecule of sodium bicarbonate produced by the stomach for alkalizing, a molecule of hydrochloric acid is produced as a waste product. Hydrochloric acid or HCL never touches the food or drink but falls into the gastric pits of the stomach away from the food and drink as the sodium bicarbonate rises to the top to alkalize the food and/or liquids ingested. This is necessary in order to prepare the food in an alkaline state for the duodenum and the small intestine where the liquid food is then biologically transformed into stem cells. There is NO part of the alimentary canal that does not secret sodium bicarbonate for alkalizing. In conclusion, the stomach is an organ of contribution and alkalizing, not a digestive organ as medical savants would have us believe. So now you know it is a whopper of a lie.

7) A cold is caused by a virus.

This is another whopper–a century long distortion. A cold is the body removing excess dietary and/or metabolic acids through the orifices of the body to maintain its delicate alkaline pH. Colds are NOT caused by viruses but are caused by eating too much acidic GARBAGE. I won’t get YOUR cold if MY body is properly alkaline. Excess acids can also be caused by your thoughts or negative emotions which can also give rise to the elimination of these acids through various orifices, such as your eyes, ears, mouth or nose.

8) Pharmaceutical drugs may have side-effects.

What an intentional obfuscation this is! Pharmaceutical drugs do not have side-effects; they have EFFECTS! And lots of them! If you take the drugs, plan on them affecting your health in many negative and acidic ways.

9) The brain and body runs on sugar.

This is closer to gross ignorance than a lie. Sugar is a metabolic acid and has no value in the body. None. Zero. Zip. Nada. The brain and body does NOT run on sugar; it runs on electrons – just like every other cell in the human body. Increase your healthy brain function with more electrons with electron-rich food and water.

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10)  Cancer is a disease of the tissues.

NO! Cancer is not a disease of the tissues but a disease of the fluids of the body. After a trillion dollars spent since President Nixon declared war on cancer, we still pretend not to know what it is. But it has become a several hundred billion dollar industry…..larger than the automobile industry. Cancer is an acidic, environmental, dietary and/or metabolic liquid; it is NOT a cell and we ALL have some of it in our body to greater or lesser degree. The more acid we have in our body, the greater the risk for cancerous tissues. Cancer therefore is a four letter word: ACID! And cancer’s fumbling, bumbling proponents have put forth another four letter word: MYTH.

11) HIV is a virus and causes AIDS.

This is an incredible whopper! And because the real and UNEXAMINED TRUTH has been explained by several scientists for many years, it is MORE than a whopper. It is now a fraud. There is NO HIV virus. You heard me right; there is NO HIV virus! There never has been. AIDS or immune deficiency is caused by an acidic way of living, eating and thinking. There is no need for drugs, but just the need to change to an alkaline lifestyle and diet and PRESTO…. NO MORE AIDS. It works 100 percent of the time if you get going before the drugs and wrong diet have taken you right up to death’s door.

12) HPV is a virus and causes cervical cancer.

This is also an incredible whopper! HPV does not cause cervical cancer. Metabolic and/or dietary acid causes cancer. HPV is another pHantom virus. It does not exist. The cause of reproductive cancers are from the acids you produce from what you eat, what you think, and how you live. You don’t get cancer you do cancer. So stop doing cancer with an acidic lifestyle and diet and start doing “Young Living” and the pH Miracle alkaline lifestyle and diet.

13) Lyme’s Disease is caused by a spirochete bacteria or a Tick bite.

Once again this is medical science at its best trying to keep the germ and infection theory alive. There is NO bacteria or spirochete bacteria that causes Lyme’s Dis-ease. Lyme’s dis-ease is nothing more than the blood trying to purify itself from excess metabolic and/or dietary acid by removing these acids out into the colloidal connective tissues. Simply put Lyme’s dis-ease is nothing more than a person who is adsorbing and absorbing their own urine into the colloidal connective tissues. The irritation and inflammation and then degeneration one feels is all caused by dietary and/or metabolic acid that has NOT been properly eliminated through the four channels of elimination – urination, perspiration, defecation and respiration. My recommendation for so-called Lyme’s Dis-ease is an alkaline lifestyle and diet with at least 2 hours of exercise daily. In other words “get off you fat or skinny ac-id! and Go To Health!”

14) Taking digestive enzymes will help digestion.

This is a major fable and fabrication to which many holistic doctors prescribe. And it’s a dangerous one….especially for people who take digestive enzymes all the time. Enzymes are acids from fermentation and are poisonous. Just like Drano, taking enzymes will eventually destroy your alkalizing alimentary canal. One will kill you fast and one will kill you slow! Digestive enzymes may break down meat, but nutritional science clearly tells us that you shouldn’t be eating meat. They will break you down too because guess what? Your alimentary canal is meat!!

15) Blood is made in the marrow of the bones.

This inaccuracy and science fiction began with the distortions of four scientists in 1952 when they conducted starvation studies on rabbits and pigeons and decided after autopsy that blood was created in the bones. This is NOT correct. The primary site of blood production is in the crypts of the intestinal villi in the small intestine. When acids (antibiotics, acid food and drink, enzymes, probiotics) damage or destroy the intestinal villi, then the body makes blood out of various body cells such as the bones. The studies on blood in 1952 may likely have been the correct conclusion if the autopsies had been done on humans–assuming the bodies had starved to death like the rabbits and pigeons. Logically, autopsies are done on people who have been very sick and finally died. The body is so sick that blood has not been made in the the intestinal villi perhaps for some time. Now medical savants have amazingly discovered that blood can also be made in the liver. The truth is that it can also be made from all the organs and all the cells once the body is sickly enough. Hopefully, we won’t be doing autopsies on healthy bodies because they rarely die. But if we did, we’d find out where blood is really made in a healthy body….in the crypts of the intestinal villi in the twenty-seven feet of the small intestine.

16) Germs cause disease via an infection.

This is another invention based on faulty scientific premises. Germs are nothing more than the biological transformation of organized matter disorganizing. Germs therefore are the RESULT of fermenting matter and not the CAUSE of fermenting matter, just as the smoke of a fired gun is not the cause but the evidence that the gun has been fired. When you see bacteria, yeast or mold on food, this is a result of food deterioration, not a result of an infection. When I see bacteria or yeast in the blood, I know this is a result of blood or body cells biologically transforming and not a result of an infection. In other words, germs are born in us and from us. The infection can only contribute to a state of imbalance but CANNOT cause ANY specific disease. So stay away from all treatment plans, traditional or alternative that focuses on the killing germs. If the drug or supplement will kill germs it will also kill you.

17) High Cholesterol in the form of low density lipoproteins or LDL’s can cause heart attacks and strokes.

Cholesterol does NOT cause heart attacks or stokes. Not a single one. This is a distortion and an inaccuracy based on faulty observation and inquiry. Environmental, dietary and metabolic acid cause heart attacks and strokes. The body releases cholesterol or LDL’s to buffer or chelate the toxic lethal affects of acid to protect the body, not harm the body. It is your thoughts, your words and your deeds that create waste products or acids. If these acids are not eliminated through urination. perspiration, defection or respiration, the body will release cholesterol or LDL’s to buffer these acids for protection and not for destruction. A recent landmark study showed that you are more likely to have a heart attack or stroke with normal or low cholesterol then a person with a total cholesterol over 300. Your risk for a heart attack or stroke increases significantly as your acid levels increase or if you lower your cholesterol with drugs without lowering your production of acid from the environment, lifestyle, diet and/or metabolism.

18) Eating protein builds muscles.

Wrong again. This is another fictitious distortion based on faulty observation based on a) preconceived notions about how the body works and b) the failure of science to sufficiently isolate variables when making so-called scientific observations. Tell the strongest animals in the world–vegetarian animals–that eating protein builds muscle. Eating protein actually makes you weak and eventually sick and tired from the debilitating acids of sulfuric, nitric, phosphoric and uric acid. The body builds muscle from blood and not from plant or animal protein. At the Ranch we grow avocados. We give our avocados minerals, water and sunshine – no protein. Yet, our avocados are 80% healthy fat and 15% protein. If you want to build muscle you have to build blood. And to build blood you have to eat green foods and lots of them.

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http://www.phmiracleliving.com/p-306-liquid-chloropheal.aspx

19) Obesity is a fat problem.

I would call this a big fat lie. A big Whopper with cheese and bacon. No, I’m sorry fat doctors, fat farms and fat clinics of the world. Obesity is an acid problem, not a fat problem. The body protects itself against acidic lifestyles and diets by making and using fat. Think of fat as your parking places for environmental, dietary, and metabolic acids that are not properly eliminated via urination, perspiration, defecation and/or respiration. You can now say that fat is saving your life. Thank you fat! Be glad that fat was not accumulating inside your veins and arteries. At least collecting on your hips and belly you could see the fat and decide if you want to do something about it. All you need to do is get off your fat acid and go to health with an alkaline lifestyle and diet. The average weight loss on the pH Miracle Lifestyle and Diet is 1 pound a day – 30 pounds in 30 days. As you alkalize the fat melts away with all of its acidic contents.

http://www.phmiracleliving.com/p-380-young-phorever-weight-loss-starter-pack.aspx

20) Hormone replacement therapy can help balance your hormones.

This greedy fiction and pharmaceutical deception is actually hurting ever so many unknowing innocent women. The first thing to understand is that hormones are acidic waste products of endocrine gland function. Balancing your hormones would be like balancing your car’s carbon monoxide exhaust. You would never give you car more acidic carbon monoxide to help it run better. You would change the oil, the filter or use a more energy efficient fuel. This is what you need to do when you have endocrine or energy imbalance. You need to change your lifestyle and diet to an alkaline lifestyle and diet with liberal amounts of electron rich green foods, lots of alkaline water and plenty of exercise. You can easily try our Deluxe Pack to start the process of endocrine balance and energy. You’ll see a difference in a very short period of time.

http://www.phmiracleliving.com/p-382-young-phorever-deluxe-starter-pack.aspx

21) Salt will cause high blood pressure and water retention.

This medical lie is a whopper. Acid causes water retention and elevates blood pressure and pulse rate. All of your body fluids are salted with sodium chloride. Salt is the catalyst for the transportation of energy. You cannot have a thought without salt. Salt is required to keep the body alkaline and preserves it from dietary and metabolic acid. If you are sick or tired you are deficient in salt. If you have sugar cravings you are deficient in salt. If you have low energy you are deficient in salt. If you have hormonal imbalance you are deficient in salt. If you have high blood pressure or if you are fluid retentive then give up your acidic lifestyle and diet not the salt. I recommend at least 12 to 14 grams of unprocessed salt every day based upon a man or woman weighing 70 kilos or 154 pounds. Salt is life. You cannot live without oxygen and you cannot live without salt!

http://www.phmiracleliving.com/p-221-phour-salts-tm-454-grams.aspx

Healthy LIfestyle Choices in Africa

My West African friends and pHROEVER YOUNG Coaches from Nigeria are sharing the “pHROEVER YOUNG Lifestyle and Diet back home with their family, friends and patients. Living in HIV and Ebola land they know that these so-called diseases are NOT caused by viruses but are caused by acidic vaccines, acidic water, acidic food and poor hygiene and sanitation. They know that an alkaline lifestyle and diet is the real medicine that will support the immune system, maintain the alkaline design of the body fluids and keep Africans free from ALL sickness and disease – including HIV, HPV, HEP C, H1N1, West Nile and Ebola.

Follow the Money!

The Great and Abominable Secret?The picture below shows genetically modified Ebola vaccines already being administered to healthy volunteers in the United States, UK, Gambia and Mali, as officials worldwide are fast-tracking the creation and approval of an Ebola vaccine. Why?

So what is the great and abominable secret?

Continue reading Follow the Money!

Ebola is to be Feared?

What is Ebola and do we need to fear Ebola?

Ebola virus (poisoning) disease (EVD), Ebola hemorrhagic fever (EHF), or simply Ebola is an acidic dis-ease of humans and other primates with an unknow isolated antigen, according to current medical savants.

Symptoms start two days to three weeks, with a fever, sore throat, muscle pain, and headaches. Typically, vomiting, diarrhea, and rash follow, along with decreased function of the liver and kidneys due to acid buildup and improper elimination of dietary and/or metabolic acidic waste. Around this time, highly acidic people may begin to bleed both within the body and externally.

Scientist have theorized that Ebola may be acquired upon contact with blood or bodily fluids of an infected animal. This theory has not been proven. Spreading through the air has not been documented in the natural environment. Fruit bats are believed to be a carrier and may spread the virus or acidic venom without being affected. This theory has yet to be proven. Once a human is thought to be affected, the dis-ease is thought to spread between people, as well. This theory has yet to be proven. Scientist also suggest that male survivors may be able to transmit the disease via semen for nearly two months. This theory has also yet to be proven.

To make the diagnosis Ebola, typically other diseases with identical symptoms such as malaria, cholera and other acidic hemorrhagic fevers are first excluded making Ebola very difficult to differentiate. To confirm the diagnosis, blood samples are tested for viral antibodies, since no viral RNA or virus has been isolated and then identified using the scientific method of Koch’s postulates.

Considering the acidic symptoms of Ebola poisoning it may be prudent to focus on restoring the alkaline design of the body rather than treating for any specific disease or disease symptom, with an unknown or identified pathogen. This can be done successfully for HIV, HPV, HEP C and Ebola by 1) detoxing and opening the channels of elimination, 2) healing the gut, 3) building healthy blood, and 4) hyper-perfusing the tissues with alkalinity.

For more information concerning viruses read, A Second Thought About Viruses, Vaccines and the HIV/AIDS Hypothesis, Dr. Duesberg’s book, Inventing the AIDS virus which also covers EBOLA and The pH Miracle revised and updated.

Sources:
1) “Ebola virus disease Fact sheet N°103”. World Health Organization. 2014-03-01. Retrieved 2014-04-12.
2) Jump up to: a b “2014 Ebola Virus Disease (EVD) outbreak in West Africa”. WHO. 2014-04-21. Retrieved 2014-08-03.
3) Jump up to: a b C.M. Fauquet (2005). Virus taxonomy classification and nomenclature of viruses; 8th report of the International Committee on Taxonomy of Viruses. Oxford: Elsevier/Academic Press. p. 648. ISBN 9780080575483.

What is the Germ? What is a Virus?

What is a Germ? What is a Virus?
A Second Thought About Viruses, Vaccines and the HIV/AIDS, HEP C, HPV, Hantavirus, SARS and Ebola Hypothesis! – Part 1
“In the sciences, people quickly come to regard as their own personal property that which they have learned and had passed on to them at the Universities and Academies. If, however, someone else now comes along with new ideas to contradict the credo (that has been recited for years and passed on in turn to others) and in fact, even threaten to overturn it, and all passions are raised against this threat and no methods are left untried to suppress it. People resist it in every way possible: pretending not to have heard about it; speaking disparagingly of it, as if it were not even worth the effort of looking into the matter. And so a new truth can have a long wait before finally been excepted.” – Goethe
Viruses
Introduction
The first isolation of the virus was achieved in 1892 by Russian that bacteria hunter Dmitri Ivowski, who gathered fluid from disease , tobacco plants. He passed this liquid through field for fine enough to retain bacteria; yet to Ivowski’s surprise, the bacteria space free filtrate easily made healthy plants sick. In 1888, a Dutch botanist, Martinus Wilhelm Beijerinck, repeating the experiment, also recognized that there was an invisible cause and named the infectious agent, “Tobacco mosaic virus.” In the same year as Beijerinck’s report, two German scientists, purified a liquid containing ‘filterable viruses’ that caused foot and mouth disease in cattle (viruses were at one time called ‘filterable bacteria’, but eventually the term ‘filterable bacteria’ came to apply only to viruses, and was the words ‘filterable bacteria’ were dropped). Walter Reed followed in 1901 with a filtrate responsible for yellow fever, and soon dozens of other disease causing viruses were found.
In 1935, another American, Wendell M. Stanley, went back to the beginning and created pure crystals of tobacco mosaic virus from a filtered liquid solution. He affirmed that these crystals could easily infect plants, and concluded that a virus was not a living organism, since it could be crystallize like salt and yet still remain infectious. Subsequently, bacteriologists all over the world began filtering for viruses, and a new era of biology was born – Virology.
Historically, medical science has a baseline on the question of whether any virus is alive. Originally, it was described as non-living, but is currently said to be an extremely complex molecule or extremely simple microorganism, and is usually referred to as a parasite having a cycle of life. (The term “Killed” is applied to certain viral vaccines, thus implying an official conviction that viruses are alive.) Commonly composed of either DNA or RNA cores with protein coverings, and having no inherent reproductive ability, viruses depend upon the host for replication. They must utilize the nucleic acids of living cells. They infect to reproduce their proteins (i.e., trick the host into producing them), which are then assembled into new viruses like cars on assembly line. Theoretically, this is their only means of surviving, and infecting new cells or hosts.
Birth of Virology — a Miscarriage?
Underlying the birth of virology was the doctrine of monomorphism — that all microorganisms (herein called microforms) are fixed species, unchangeable; that each pathological type produces (usually), only one specific disease; that microforms never arise endogenously, i.e., have absolute origin within the host; and that blood and tissues are sterile under healthy conditions. This last point warrants immediate comment. Theoretically, under ideal health conditions, the blood might be sterile, though it has the inherent potential to develop morbid microforms, as discussed in my book, Sick and Tired. Long and repeated observation of live blood in the phase contrast, darkfield microscope, however, shows that the blood can contain various microforms and otherwise asymptomatic host, or in a condition defined as normal or healthy in orthodox terms. The forms are easily visible before other physical symptoms arise. (Since long and repeated observation has correlated their presence with other disease symptoms and their disappearance with the return of health, they serve as indicators of impending outward signs of disease).
Monomorphism was the cornerstone of developments in 20th-century medical research and treatments. Refusal by the mainstream to examine fairly, much less except, the demonstrated fact of pleomorphism — that viruses and bacteria (and also yeast, fungi and mold) are evolutions from a small indestructible anatomical element, I referred to as the microzyma. That microforms can rapidly change their form (evolve and “devolve”) in vivo, one becoming another dependant upon conditions in the inner terrain (environment); that blood and tissues are not necessarily sterile; and that there are no specific diseases, but only specific disease conditions — was the foundation of a latter-day “Galileo debate.” It is so-called because those who wore the “robes” of scientific authority just like today, reprising the religious fanatics who punished the noted astronomer for his truth, would not be swayed from folly when presented with its contrary theory. These truths began in earnest with Antoine Bechamp in the 19th-century (who also endured the indignation of a fanatical clergy).
In the early third of the 20th-century, the heated debate took place over ‘filterable bacteria’ versus ‘non-filterable’ bacteria. This was a major battle concerning micromorphology (discussed briefly below). The orthodox view prevailed: bacterial forms were not small enough to pass, or did not have a smaller, earlier stage. What passed through ‘bacteria proof’ filters was something else, i.e., viruses. Standard medical textbooks, long made this filtering distinction between bacteria and viruses. Subsequently, however, the cellular nature of many filterable forms originally thought to be viruses, such as some mycoplasmas, rickettsias, and various other groups, has been established. In this writer’s opinion, with the victory of the monomorphic view, deeper understanding of infectious ‘disease’ was lost, setting the stage for cancer, degenerative symptoms, HIV. AIDS, Ebola, Hantavirus, Hep C, HPV, etc.
What You See?
A typical bacteria is about 1 micron in size. Most filterable bacterial forms now called viruses range in size from .3 microns (300 millimicrons) to .01 microns (10 millimicrons) — particularly in the colloidal range (.1 to .001 micron). Most of the larger viruses are a third to a quarter the size of the average bacteria. And size is critical because .3 microns is the resolution limit of modern-day light microscopes. Thus, as viruses were discovered (except for the very large ones, such as mumps), they required an electron microscope to be seen, especially given the the fact that Royal Rife’s microscope technology and career were destroyed by vested interests. Unfortunately, electron microscopes and the process of chemical staining disorganize or damage all specimens, whereas Rife’s technology allowed life to proceed and thus evolve under its lens. As viruses became visible to advancing technology, the ratification was that the technology revealed, two minds infected with monomorphism, protein structures deemed foreign in the body.
A New Theory
Formulated by Antoine BeChamp in the 19th-century, the microzymian principal is the basis of the new theory about ‘viruses’. Recently, this principle holds that in all living organisms are biologically indestructible anatomical elements, which BeChamp called microzymas. They are independently living organized ferments, capable of producing enzymes and capable of evolving into more complex microforms such as bacteria, yeast or mold. Bechamp’s thesis, is that disease is a condition of ones internal environment (terrain); that disease (and its symptoms) are “born of us and in us.”; and that disease is not produced by an attack of micro entities, but calls forth their endogenous evolution.
My studies and research suggests that the complexes, science calls viruses and retroviruses originate in the cell, as the microzymian as the principal suggests. However, they are created in response to an alarming acidic situation (condition of disease) for the purpose of genetic repair. They are repair proteins, evolved from anatomical elements (microzymas), not pathogenic microorganisms.
It is known that normal cell activity includes genetic repair. Both enzymes and proteins must be involved. What is the mechanism?
Viruses are organized around DNA or RNA, not both. Thus, they are quite probably intended to repair genetic molecules or other structures, and show up with disease symptoms, because the body needs them. Since viruses require a living cell/host for reproduction, how do we know that the scenario is not set in motion, for a purpose by the cell (i.e., it’s microzymas), rather than being the result of invasion? Because disease (disturbance of balance in the organism) is so prevalent, especially that which is not yet becoming indicated by common symptoms, repair proteins may be frequently or constantly present. A toxified cell may easily suffer localized damage to the genome. Since most observers are not even aware of the microzymian principal, much less understand or even consider it, and since monomorphism stresses invasion, these proteins complexes are regarded as foreign and disease is attributed to them.
Another note of interest is the size of viruses compared to the microzyma. Viruses are considered to be some of the smallest biological particles and are frequently of colloidal size: e.g., hepatitis A, 27 nanometers (.027 microns); hepatitis B (.042 microns); polio virus (.03 microns); EBV (.042 microns); HIV (.080 to .12 microns); influenza (.08 to .12 microns); mumps (.15 to .30 microns); smallpox (.30 microns); and, according to BeChamp, the microzyma (.0005 microns).
In his book, ‘The Blood and its Third Anatomical Element’, Bechamp states: “the microzyma is at the beginning and at the end of all organization. It is the fundamental anatomical element whereby the cellules, the tissues, the organs, the whole of the organism are constituted living . . . . in a state of health, the microzymas act harmoniously and our life is, in every meaning of the word, a regular fermentation. In the condition of disease, the microzymas do not act harmoniously, the fermentation is disturbed, the microzymas have either change their function or are placed in an abnormal situation by some modification of the median. The virus is either a self-ordered microzymian polymerization, or (less likely), a structure made by microzymas. It is envelope in protein which is also composed of microzymas, and could well be thought of as an autonomous molecular tool box.
Along with doctors Glen Dettman and Archie Kalokerinos, I wonder, “whether Bechamp’s writing anticipated, in some respects, the discovery of RNA and DNA?” Could the genetic structure be the construct, thus a tool, of the microzyma? They quote a personal communication [1974] from a professor Bayev of the former USSR Academy of Sciences, who discusses his work showing the molecular self- restoration from its parts of pure transfer RNA from brewers yeast is possible.
In my own research I have found molecular restoration similar to that described by Bayev. In my experiment , I used 10-year-old coagulated capillary blood from a woman with cancer. With one drop of .9% of sodium chloride, the blood was restored to an appearance and level of activity characteristic of freshly drawn sample of blood. In other words, the anatomical microzymas of the dry blood were restored to activity. Even the white blood cells became active again. One might eagerly asked for explanation of the reversal of polymers made during clotting. It is unclear at this point how this reversal takes place, except to say that what can evolve apparently has the potential to devolve. It is observable, however. For example, I have seen, and recorded on video, rod microforms retro-grading without any visible decomposition from 10 microns in length to the vicinity of .1 micron.
This research supports the very important postulates that the cell is not the smallest living biological unit, as promulgated by conventional medical science. In fact, a smaller biological unit is the imperishable micros I’m a, which is an organized, living been “of a special category without analog,” said BeChamp, who found them ready to become active in chalk deposits at least 11 million years old.
The Pleomorphic Cycle
I suggest a developmental cycle in vivo consisting of three macro stages: [1] a primitive stage comprising the repair proteins complexes; [2] an intermediate, or bacterial, stage including filterable forms such as the cell wall deficient forms described by Lida Mittman, PhD. [in Cell Wall Deficient Forms, Stealth pathogens]; and [3] a culmination stage consisting of yeast and fungal phases, and then mold, the and phase. The usual course of development would be from microzyma to repair proteins, and then to bacterium, etc. However, under certain conditions, such as, for example, it is highly likely that the microzymas can skip the primitive stage and become bacteria directly. Although these transformations are as astounding as that of a larva to a butterfly, what is equally impressive under observation is in the rapidity with which they can take place — in minutes, even seconds, sometimes. By the same token, when provoked by acidic conditions and the cycle proceeds to yeast, fungus and then mold, it may occur so rapidly that the bacterial stage, if that happens, has no time to be of any significance.
Thus, symptomgenic microforms can originate within the higher organisms without invasion, via a permutation of the endogenous microzymas when the situation calls for such change. The situation is an imbalance referred to by Bechamp as a “modification of the median.” Endogenous evolution is evident under the microscope when bacterial, yeast, and fungal forms are seen coming out of the red blood cells, which initially appear normal.
Biological Basis for the Pleomorphic Cycle
There is a common biological basis for the pleomorphic cycle and its increasing complexity of organization: more complex forms evolve inherently upon the death of an organism for the purpose of recycling its anatomical and chemical structures in the carbon cycle. The process of rapid evolution [which is reversible] is an essential life process, which, beyond the repair stage, is necessary to return a dead organism to the earth. The second and third stage microforms degenerate the body’s vital substances and tissues via putrefaction [bacteria] and fermentation [yeast and fungus].
Fermentation results in acidic waste products, which further breakdown tissue. Disease symptoms, then, especially the degenerative type, are NOT produced by viruses, but manifest as chemical decomposition, or attempted recycling via fermentation and acidic toxins, but with ‘host’ survival processes still, operable. Obviously, certain other factors may play important roles in producing symptoms, such as heavy-metal toxicity, or state of mind, for example. Some of the body survival methods also produce symptoms commonly called dis-eases. An example is eczema, and emergency expulsion of acidic toxins via the pores of the skin.
The aforementioned casual [alarming] situation, or modification of the median, is chronic tissue acidification [pH imbalance] and oxygen deprivation in the blood and tissues due to acidic forming foods, adverse lifestyle, emotional stress, and environmental stress. This is not an oversimplification! Acidification/hypoxia biochemically signals a dead host to the microzymas, while creating collapsed areas [dead zone’s] of the colloidal system in the intercellular fluid, and it is the primary physiological disease condition at which the symptoms commonly called specific diseases arise.
Thus, we distinguish between this disease condition and its consequent symptoms, which include both the morbidly evolved microzymas and the physiological science commonly thought of as specific diseases. As they develop, microforms [bacteria, yeast, fungus and mold] are actually scavenging forms of the microzyma, developed when disease in the cell life requires tissue to be broken up. These upper development forms are the ones easily visible in the blood before physical symptoms arise. They disappear, [devolve] when the recycling task is complete, once again becoming microzymas of the earth and/or air.
Virus or Liquid or Solidified Toxin/Acid?
Regarding the early period of virus isolation, a question is whether the unseen entities isolated in filtered fluids were accompanied by the waste products [mycotoxins] of fermentation by yeast and/or fungus of cellular elements, such as DNA. If virus infiltrates are injected into a host to prove virulence, it is almost certain that easily filterable molecular toxins will be introduced as well. Could Dr. Stanley’s “pure crystals of tobacco mosaic virus” have been crystallized acidic toxins? If so, they would certainly be highly symptomgenic, as are exotoxins at the intermediate stage of the cycle, for example. However, it is not proof of anything that you can create illness by poison injection, except proof of that tautological fact.
In my research utilizing darkfield and phase contrast microscopy, it is common to see acid crystallization’s in the blood. It is normal for the body to use calcium or other mineral salts, and fats as well, to chelate the acidic waste products from the morbid fermentation of body proteins, fats and sugars. Such crystal deposits are found in cancer tissue as well. A malignant tumor removed from the breasts of one of my research clients was found to have numerous calcium deposits attached to it. It is an attempt to render inactive acidic substances that make our inner streams healthy, poison our cells, and coagulated colloidal systems in blood and intercellular fluid.
The term “virus” is the Latin word for poison, and gives us insight into the immediate cause of disease symptoms — poison is: exotoxins and mycotoxins, and a toxin, exotoxins, and toxins from environmental sources, [many of which are primary or secondary mycotoxins.]. Orthodox medicine is well aware that it is bacterial toxins more than the bacteria them self. [They feed in-house], that caused the symptoms referred to as infectious disease. Little if any emphasis is placed on this fine, but important distinction. Always, the germ is emphasized. There is little too, no awareness [or knowledge that], either, of the same role played by acidic toxins of the culminate microforms of the pleomorphic cycle. Their action and the body’s response to them are frequently ascribe to viruses, which do not produce toxins because they are the toxin or acid, but are said to wreck havoc by a number of other means. However, if they participate in symptom at Genesis in a host it is because they are stimulated to evolve into more complex, toxic genetic forms.
Somewhat less likely is the possibility that they cause damage as a result of erroneous construction or function, for one reason or another — missing mineral nutrients leading to alkaline mineral deficiencies, for example.
Misconception Breeds Contempt
In addition to chemical toxicity, however, what is the impact of the fear [emotional toxicity] that the word “virus” brings to mind and heart? It has been said that fear it is the most deadly of disease conditions. If the “disease” kills one person, the fear of it may kill 20. General prejudice concerning the danger of viruses is fundamental biological error based on Louis Pasteur’s germ theory, and is itself a perpetrator of auto-suggested illness. For example, in Africa doctors attribute some AIDS sickness to “voodoo death” syndrome, the term for illnesses induced psychologically. According to one nurse, “we had people who were symptomatically AIDS patients. They were dying of AIDS, but when they were tested and found out they were negative they suddenly rebounded and are now perfectly healthy.” Ironically, if the germ theory were found on facts, it would be correct to fear viruses, except there would be few, if any, humans living to discuss the issues. These so-called pathogenic entities are to researchers, medical practitioners and the press what criminals are to detectives — the focus and justification of their existence.
The Encyclopedia Britannica has this to say about bacteria, which relates also to viruses:
“The common idea of bacteria in the minds of most people is that of the hidden and sinister scourge lying in wait for mankind. This popular conception is born of the fact that attention was first focused upon bacteria through the discovery, some seven years ago, of the relationship of bacteria to disease in man, and that in its infancy, the study of bacteriology was a branch of medical science. Relatively few people assigned to bacteria, the important position in the world of living things that they rightly occupied, for it is only a few of the bacteria known today that have developed in such a way that they can live in the human body, and for everyone of this kind, there are scores of others which are perfectly harmless and far from being regarded as the enemies of mankind, must be numbered among his best friends.
It is in fact, no exaggeration to say that upon the activities of bacteria. The very existence of man depends; indeed, without bacteria there could be no other living thing in the world; for every animal and plant owes its existence to the fertility of the soil, and this in turn depends upon the activity of the microorganisms which inhabit the soil in almost inconceivable numbers. It Is one of the main objects of this article to show how true is this statement; there will be found in it only passing reference to the organisms which produce disease in man and animals — for information on these see Pathology and Immunity. [Encyclopedia Britannica, 14th ed., Volume 2, page 899].
The general message of the foregoing article applies even more aptly to viruses in the sense that much fear has been bred and cultivated around them, although they never produce disease symptoms, whereas the acid waste products of bacteria, yeast, fungus and mold do. The writer of the above understands bacteria, with the exceptions that symptomgenic bacteria found in man and animals do not produce disease. [Only secondary symptoms], that their precursors are endogenous to higher organisms, and they have not “developed in such a way that they can live in the human body.”
If anything, the reverse is true. According to one theory of microbiology, microforms have colonized over eons to become higher organisms. In one sense, then, the human body has developed as a specialized environment for them.
An important dimension of the bacterial dependence of higher life forms is the floral population in the human digestive tract. Literally, these “foreign species” keep us alive. Most bacteria have the same underlying function, whether found in the soil, sewage, in the human digestive tract, or elsewhere in nature: they are an essential part of the life processes of hire organisms. They will not or cannot attack healthy cells or tissues, but certain ones will recycle sick or dead tissue in much the same way insect pests are drawn to weaker plants. As Bechamp said, “nothing is the prey of death; all things are the prey of life.”
Following in the wake of misconceptions arising from the fundamental biological error known as the germ theory of disease, defying infiltrates of disease tissue as a newly discovered infectious microforms was the birth of a major corollary error in bio science.
Viral Behavior Reconsidered
Listed below are ways of viruses are said to disrupt or destroy host cells. According to orthodox medical science and the germ theory advocates. Following each in its italics is a different interpretation following from microzymian principle:
1. Viral proteins insert into the host cells , plasma membrane and directly damage its integrity , to promote cell fusion [HIV, measles, and herpes viruses.].
Proteins are attempting to repair membrane damage, or enter cells to repair other proteins. There is the question as to whether viruses on cell walls are coming or going. In both cases, it would be a matter of whether or not a cell has been disturbed by excess fermentation and acidity. But in the former case, the cell would be dysfunctional before attachment occurs, thus requiring the repair complex. Another possibility, perhaps remote, is that dysfunctional receptors on cells are in need of repair, or they are covered by these complexes to inactivate malfunction of the cells. Positive electrical charges in a compromised acidic terrain, primarily on acidic molecules from fermentation’s, discharge cell membranes and act as mortar to stick cells together causing rouleau and clotting.
2. Viruses inhibit a host cell DNA, RNA, or protein synthesis. For example, polio virus inactivates cap-binding protein, which is essential for protein synthesis, directed by capped host cell mRNA’s, while allowing protein synthesis from uncapped polio virus in mRNA’s.
Protein inactivation is probably being done by fermentation or by acidic toxins from fermentation, while “poliovirus” is produced in the cell to reverse the damage.
3. Viruses replicate efficiently and lyse host cells, e.g., liver cells by yellow fever, and neurons by poliovirus.
Highly unlikely. The lysing is more likely caused by acidic mycotoxicosis, or by free radicals released in response to mycotoxic stress, or from other sources [I lysine radiation, for example]. Repair particles are residual after cell wall disruption.
4. Slow-virus infections [e.g., sub acute sclerosing panencephalitis caused by the measles virus] culminate in severe progressive disease is after a long latency period.
How is this demonstrated? Perhaps “latency” is a period of unsuccessful or attempted repair that eventually falters. Symptomology naturally appears in the weakest parts of the body. Excess acidity is always a systemic problem that localizes, just as cancer is a systemic acidic condition that localizes, even though it its symtogenic influence may later spread.
5. Viral antigen proteins on the surface of the host cells are recognized by the immune system, and the host lymphocytes attack, the virus infected cells [e.g., liver cells infected with hepatitis B].
Liver cells are damaged beyond repair by exotoxins and mycotoxicosis, and the immune system, our elaborate janitorial service, is cleaning out the garbage. Perhaps the repair protein antigen is expressed to signal any in response [because the cell is beyond repair], which is one explanation for why there are antibodies to these proteins.
6. Viruses damage cells involved in the host anti-microbial defense, leading to secondary infections.
The function of immune cells are damaged by bacterial or fungal waste products/acidic and/or overworked by toxic acidic overload, preventing proper cleanup and elimination of disharmonious, symptomgenic elements.
7. Viral killing the one cell type causes the death of other cells that depend on them, e.g., degeneration of muscle cells enervated by the attack of poliovirus on motor neurons.
Once again, a misinterpretation and lack of understanding that is not viral microforms that damage neurons. Acidic toxins from bacteria, yeast, fungus and mold — as well as the ferments of glucose, uric acid from proteins, hormones and acetic acids from fats — produce, or influence the body to produce, dis-ease or inflammatory symptoms. Not recognizing “virus,” for what it is, observers attribute dis-ease or disease to it.
8. Host cell responses to viruses include metabolic derangement and transformations resulting in neoplastic changes.
Metabolic derangement has occurred prior to the appearance of repair proteins, due to toxic overload in the cell. It is more likely that the proteins attempt to prevent cell transformation, and that cancerous development is cell conversion from primarily oxidative to wholly fermentation of metabolism, mediated by yeast, fungus and mold.
9. According to orthodox theory, viruses enter a host cell and replicate at the host’s expense. Replication is accomplished using enzymes, which are distinct for each virus family. For example, RNA polymerase is used by negative stranded RNA viruses degenerates positive stranded mRNA, or as reverse transcriptase is used by retroviruses to generate DNA from their RNA template and to integrate that DNA into the host genome.
It is normal for repair proteins to generate enzymes or acidic waste products as they do their work of repair.
10. one reason suggested for viral tropism [the tendency to infect some cells, but not others] is the presence or absence of host cell receptors that allow the virus to attach. It is said, for example, that HIV binds to the proteins [CD4] involved with antigen presentation on a helper. The lymphocytes, that Epstein-Barr virus binds to the complement receptor [CD2] on macrophages, that rabies virus binds to the acetylcholine receptor on neurons, and that rhino viruses bind to the adhesion proteins [ICAM-1] on mucosal cells.
See answer to number 1 above.
Theoretically, once attach, the entire virion, or a portion containing the genome and essential polymerases, penetrates into the cell saddle plasma in one of three ways: [one] translocation of the entire virus across the plasma membrane; [two] receptor mediated endocytosis of the virus and fusion with endosomal membranes; or , [three] fusion of the viral envelope with the cell membrane. Theory suggests that within the cell the virus uncoats, separating its genome from its structional components and losing its infectivity before replication. In either the nucleus or the cytoplasma, newly synthesize viral genomes and capsid proteins are assembled into progeny virions, which may then bud to the plasma membrane. Unencapsulated viruses may be released also, directly through the membrane.
It is interesting, however, that viruses can somehow choose the “infection.” To be aborted, latent or persistent, meaning respectively: [one] viral infections with incomplete replication cycles; [two] persisting in the cryptic state, like herpes zoster within a dorsal root ganglion, which suddenly becomes active to produce shingles; [three continuously synthesized virions, with or without altered cell function [e.g., hepatitis B]. These three ideas, especially latency, have arisen as feeble excuses for the untenable virus theory.
11. In order for viruses to reproduce, they must complete the following four steps:
a] Adsorption and penetration of the cell. The viral particle binds to the host cell membrane. This is unusually a specific interaction in which a viral encoded protein on the capsid or a glycoprotein embedded in the virion envelope binds to a host cell membrane receptor and is then internalized. This internalization occurs by endocytosis or by fusion of the virion envelope with the host cell membrane.
This is the mechanism whereby the viral particle enters the cell for the purposes of carrying out repairs to the damaged DNA or RNA.
b) Uncoating of the virus, so that the nucleic acid can be released from the capsid into the nucleus or cytoplasm.
Repair work may require uncoating. An uncoated “virus” in the saddle plasma, may have, from the nucleus and not yet have a code, as in the case of hepatitis B , according to medical science.
A coat is then created to protect the nucleic acid, to make a communicative or response to protein complex, or to allow exiting the cell for remote function or for neutralization and recycling by the immune system.
c) Synthesis and assembly of viral products, as well as in addition of the host cell’s own DNA, RNA and protein synthesis.
Protein complex is produced in response to an alarming acidic situation — fermentation and mycotoxic stress — are capable of self-reported replication. As suggested by Bechamp, the microzyma is specific for each organ, therefore specific repair proteins will be needed for specific cells that make a specific organ that are being disturbed by dietary and/or metabolic acidic waste products. There is the question of why the great numbers in some cases. One possibility is simply over reaction; for example, fever can be extreme. Why? To remove dietary, metabolic acids or acids from bacteria, yeast, fungus and/or mold.
d) And finally, release of virions from the host cell either by budding or lysis.
[1] Complexes leave the cell for remote function or to be neutralize; [2] repairs have failed, and complexes are released prior to or during the breakdown of the cell by acidic toxins or the immune system.
Further Considerations
Virologists referred to certain microforms as passenger viruses, which are present in asymptomatic situations, riding on their host genetic molecule like a passenger. To the conventional mind searching for new diseases or for viral cause of unexplained ones, they are most interesting, because the status virologist in the scientific community depends upon the pathogenic potential of the viruses they study. Due to their location, passenger viruses are thought to have much disease potential, thus their true function goes unnoticed. These colloidal passengers are the silent majority of animal and human intranuclear proteins essential for genetic repair.
Kalokerinos and Dettman quote Dr. Fred Klenner regarding the changeability of viruses, “I am of the opinion that virus units have the potential of going from one type to another by altering their protein coat. We see chickenpox at Thanksgiving, mumps at Christmas, read measles in the spring, and polio and Coxsackie in the summer.” Seasonal appearance of different forms may be mediated by variations of imbalance in the biological terrain or nutritive median due to the fermentation of dietary excesses such as sugar and animal proteins that accompany holidays and seasons, calling for different repair proteins. For example, outbreaks of polio have been associated with sugar consumption in summer. Various psychoemotional stresses correspond to the seasons as well.”
Supporting the general idea of dietary culpability is a statement published by the great English physician, Sir Robert McCarrison in 1936: “obsessed with the invisible microbe, virus, protozoa as all-important excite tens of disease, subservient to lavatory methods of diagnosis, hidebound by our system of nomenclature, we have to forget the most fundamental of all rules for the physician, but the right kind of food [nutrition] is the most important single factor in the promotion of health and the rhonchi to food. The most important single factor in the promotion of disease.”
Six years before BeChamp identified the microzyma as a ferment and, with his devoted associate, Professor Estor, began a 13 year odyssey of research into its nature. Florence Nightingale published a statement about the germ theory, In ‘Notes on Nursing’, first addition, 1860, she said of infection:
“Diseases are not individuals arranged in classes, like cats and dogs, but conditions growing out of one another.
Is it not living in a continual mistake to look upon diseases, as we do now, as separate entities, which must exist, like cats and dogs, instead of looking upon them as conditions, like a dirty and a clean condition, and just as much under our own control; or rather, as the reactions of kindly nature against the conditions in which we have placed ourselves?
I was brought out . . . . distinctly to believe that smallpox, for instance, was a thing of which there was once a first specimen in the world, which went on propagating itself in a perpetual chain of dissent, just as much as that there was a first dog, [or a first pair of dogs], and that smallpox would not begin itself anymore than a new dog would begin without there having been a parent dog.
Since then, I have seen it with my eyes and smelt it with my nose smallpox growing up in the first specimens, ear in close rooms or in overcrowded wards, where it could not by any possibility have been ‘caught’, but must have begun. Nay, more, I have seen diseases begin, grow up, and pass into one another . . . . I have seen, for instance, with a little overcrowding, continued fever grow up; and with a little more, typhoid fever; and when little more, typhus, and all in the same ward or hut.
Would it not be far better, truer, and more practical, if we looked upon disease in this light? For diseases, as all experience shows, are adjectives, not noun- substantives.”
That is, symptoms [called diseases] are described first of the situation.
I find legitimate BeChamp’s conclusion that what are called germs of the air are fundamentally microzyma’s of beings, which are being consumed by the recycling process, i.e., some kind of vegetative digestion — putrefaction or fermentation. In short, there are no pre-existing disease germ species. The principals of microbial medicine constitute a fundamental biological ERROR!!!!!! As BeChamp said, “the microbial doctrine is the greatest scientific silliness of this age.” This is not to say there is no transmission, only that invasion is not necessary for symptogenesis, nor is it the primary mechanism for illness. It is to say that for transmission to take place, susceptibility in the form of a compromised terrain must pre-exist in the receiver, who was then likely to be ill anyway. With the exception of the immune component in the mucosal barrier, primary host “resistance” is a function of terrain condition rather than immunity per se.
Phantom Viruses
Hepatitis
Hepatitis can be a painful symptom that has yielded profitable virus hunting opportunities in recent years. Although there are several categories of this disorder, three main varieties of what is called “acute viral hepatitis” exist: Type A [formally, ‘Infectious hepatitis’], Type B [formally ‘Serum hepatitis’], and hepatitis Type C (formally ‘non A, non-B’]. The corresponding viruses are HIV, HBV, and the non-A, non-B ‘group’, now called C. Type A is said to be caused by an RNA virus, spread primarily by fecal contamination of water and food, with blood and secretions also possibly being infectious [but it is due to the acidic toxins associated with unsanitary conditions]. Hepatitis B, discovered in the sixties, is said to be caused by a DNA virus, which replicates in the hepatocyte nucleus and receives its surface coat in the cytoplasma. It is said to be transmitted by transfused blood or blood products, or via common use of needles by intravenous drug users [but it is due primarily to over-acidification from the drugs, especially heroine. The exchange of body fluids into the blood, whether by sterilize needles, abusive sexual activity, eccentric sexual activity, etc. can also play a role overtime, because of repeated immune stress caused by foreign proteins]. Third World babies with poor nutrition and unsanitary conditions around the time of birth are also susceptible.
The third type of hepatitis, discovered in the seventies, is found among drug users and alcoholics, and accounts for 80 to 90% of hepatitis caused by blood transfusion. It is thus akin to B type and was at first thought by scientists to be hepatitis B until thorough testing a subject revealed no virus B nor A, for that matter. It was thus called “non-A, non-B” hepatitis and thought to be at least two viruses and perhaps more.
In 1987 scientists believed they found a single virus causing the third type, what is known today as the hepatitis C virus. However, what they identified was an antibody, they associated with a virus. Now, just as with HIV, they could test patients for antibodies against an elusive or invisible phantom virus. With this new observation, however, new paradoxes confronted the viral hypothesis. Huge numbers of people testing positive for the Phantom C virus never developed any symptoms. Hepatitis C is truly the result of an over-acidification or toxification of the largest filter organ in the body by such substances as lactic acid, acetylaldehyde and ethanol alcohol — not the disease of a pathological phantom virus. It is interesting to note also that all these hepatitis viruses have incubation periods of two to 25 weeks, violating Farr’s law, [see below], yet are not classified as slow viruses. Also, the point at which a “natural invasion” takes place, as opposed to a highly artificial in objective one, and thus, how true incubation periods are determined, is another interesting question. Bottom-line there is no Hepatitis C virus.
Hantavirus
A recent example of unwarranted panic in American bio medicine was the eminent hantavirus of 1994. Presumably, it had jumped species, from mouse to man [the American Navajo Indians]. However, after supposedly killing a number of people, this phantom virus apparently made peace with the Indians and retired to its mouse reservoir. The virus failed to materialize. A front-page article in the San Francisco Chronicle reported that CDC “epidemiologist across the nation are carefully monitoring the deer mouse population and the level of virus within it.” But all that was left to discover of the former. “Navajo flu” by the CDC epidemiologist [shown in their space suits] were healthy mice in the mountains. The Navajo flu is nothing new to the Native Americans and is most likely tied to sanitation, nutrition and lifestyle.
Ebola
In May 1995 , the CDC announced the new, threatening Ebola virus. The deadly killer virus was expected to leave its hidden reservoir in the rain forest of Africa to claim Europe and the United States. An article in Time magazine was peppered with men in space suits and color electron micrographs of the virus [even though electron microscopes cannot take color pictures and the pictures were of parasites]. A CDC virologist suggested the virus could leave the rain forest a if “we get a virus that is both deadly to man and transmitted in the air.” We are thus asked to fear the false image of virus somehow being launched into the air, perhaps by injection from a host, and then floating on a killer breeze to other lands. A more imaginable scenario was suggested by European epidemiologist who heads the United Nations AIDS program. Echoing the the CDC’s alarm, he stated, “it’s theoretically feasible. Then infected person from Kuwait could go to Tunisia, get on a plane to New York, fall ill, and present transmission risk there.” But within a month, the virus had disappeared in Africa, and not a single Ebola case was reported in the United States or Europe.
The World Health Organization announced on December 19, 1995 that the Ebola virus epidemic that killed 245 people in West Africa was over. All tests on any remaining suspected cases were negative. A somewhat unsettling revelation was that every Ebola outbreak in Africa, “is associated to have spread to public hospitals.” As it turned out, it was associated with reused hypodermic needles in these hospitals. Just like hantavirus, Ebola vanished, never to be heard from again, until NOW! Most interesting is that this so-called epidemic, as epidemics will, stopped without vaccines or other drugs. Consider the impact such stories have made upon our minds and on the way we view and understand germs. What’s next in the virodrama, the Andromeda strain? NO! Here we go again with the same old phantom viral story!
There is one insidious possibility that must be mentioned in passing. Some mysterious outbreaks of the past have shown years later to have been man-made. In some cases, government agency have used the public to test releases of organisms and weak biochemical acidic toxins in order to verify, through medical reports, expectations of bio-warfare activity. These incidents and the whole story of such behavior is well documented in the book, all higher forms of killing by Robert Harris and Jeremy Paxman [Hill and Wang, 1982]. In this scenario, the cause of such an incident would be constructed officially, or left as a mystery, in order to draw attention away from the truth.
To read Part 2 and Part 3 and for all references for this article read Sick and Tired by Dr. Robert O. Young – www.phmiracle.com orwww.phmiraclebooks.com

Koch’s Postulates and HIV, AIDS, HPV, HEP C, Hantavirus, Ebola, SARS, West Nile Virus, and Many More Phantom Viruses

What ARE Koch’s Postulates?

Koch’s postulates are a set of conditions long accepted as the requirements for establishing a fixed microorganism, filterable bacteria (virus), bacteria, yeast, and mold in the cause of a specific disease. The case for HIV, AIDS, HPV, HEP C, Hantavirus, Ebola, SARS, as with the identification of any causative infectious agent, should depend upon meeting these parameters, of which there are four.

The Four Parameters That Constitutes Proof That a Germ/Virus Esists and Causes A Disease!

1)  The germ or virus must be found in all cases of the disease.  Tissues said to be affected by HIV, AIDS, HPV, HEP C, Hantavirus, Ebola, SARS, etc., including primarily the white blood cells of the immune system, particularly the T-cells, the brain neurons in dementia, skin cells in lesions, such as Kaposi’s sarcoma, as well as, theoretically, any cell in the body expressing the CD4 surface receptor said to be the key to germ or viral entry.

The abundance of uninfected T-cells, about 1 in 500, in all patients is the definitive argument against the false claims for high cell-wall particle ‘loads’ or ‘burdens’ in infected patients.  The absence of active, infectious unidentified virus automatically disqualifies HIV, AIDS, HPV, HEP C, Hantavirus, Ebola, SARS, West Nile, Epstein Bar Virus as a player of disease.

2)  The germ or virus must be isolated from the host and grown in pure culture,  Even for the most experienced virus hunter, a virus that is so extremely scarce is difficult to find.  Only with rare luck and extreme persistence has ANY virus been extracted from an antibody-positive person.  This amounts to finding the proverbial needle of HIV, Ebola, etc. haystack of human DNA.  This difficulty speaks to HIV, AIDS, HPV, HEP C, Hantavirus, Ebola, SARS, West Nile, Epstein Bar, Etc. lack of potential in causing ANY disease.

3) The purified germ or virus when isolated must cause the disease again in another host.  There is no animal or human model for HIV, AIDS, HPV, HEP C, Hantavirus, Ebola, SARS, West Nile, Epstein Bar,  Swine Flu, etc., and where there is NO animal or human model, you cannot establish Koch’s postulates.  Is is even more than disconcerting to think of the number of primates that have been injected to this day in an attempt to produce, HIV/AIDS, HPV, HEP C, Hantavirus, Ebola, SARS, West Nile, Epstein Bar, Swine Flu, Etc., without success.  All of these virus’s have received a special dispensation from Koch’s postulates.

4) The germ or virus must then be isolable from the newly infected host.  We are now back to problem 2!

The Antibody That Isn’t Theory!

According to germ or viral theory, an antibody is a certain antidote for a pathogen.  According to the viral theory, however, the more antibodies you have to ANY so-called virus, the sicker you get you are said to be HIV, HPV, HEP C, EBOLA, Hantavirus, Epstein Bar, etc., positive.  You are told by your Doctor you have a disease without ANY identified viral load!  Being diagnosed with a virus is the only ‘disease’ in the allopathic file cabinet in which antibodies and now symptoms without antibodies are used to diagnose a disease.  This defies every known law, rule, guideline, fact, and behavior in the germ or viral theory book!  It is also unbelievable that vaccine research proceeds on the basis of producing antibodies, which are acid buffers and protect the alkaline design of the body, on the basis of producing antibodies to HIV, HPV, HEP C, Ebola, Hantavirus, Epstein bar, Swine Flu, etc.  Apparently these, ‘synthethic vaccines’ designed by man will signal recovery, while the body’s own antibody production signals death!!!!!  Am I missing something here?  What is this ALL about?

Bottom-line ALL of the virus’s mentioned above have received a free pass to existence and disease causing without meeting Koch’s postulates!  This is the reason I call them ALL pHantom Viruses!

To learn more about virus’s, vaccines and HIV, HPV, HEP C, Ebola, etc. read, Sick and Tired by Dr. Robert O. Young.  And you might enjoy reading the rest of the story concerning what is wrong with the autoimmune theory.  To get a copy of Sick and Tired go to: http://www.phmiracle.com or http://www.phmiraclebooks.com

Parasite of Virus?

Don’t you find it interesting that the NEWS Agencies around the World have been talking about how dangerous this Ebola virus might be or become and then putting up a picture of a parasite! WHY? Because there is NO PICTURE of Ebola. No scientist in the World has identified it under Koch’s postulates. This is why it is called a pHantom virus. It doesn’t exist. Do we know of any other so-called viruses that this has been done with? YES! Here are a few more pHantom viruses, with the biggies, HIV and AIDS, Hep C, HPV, SARS, West Nile, just to name a few. Even the Noble Priize winner in medicine for his discovery of the HIV antibody (not virus or antigen) has stated that HIV does NOT cause AIDS!. He is no longer at the University of Paris but is doing his research in Beijing, China. Do you wonder why? When I was with Dr. Luc Montagnier in Milan, Italy as a KEYNOTE SPEAKER, just 2 years ago, he made several statements at the Conference on the importance of acid/base chemistry in human health and antioxidants in the prevention and reversal of HIV and cancer. I was surprised, shocked and happy all at the same time.

So What is a Virus? What is a Germ?

 After 25 years of research, studying the affects of lifestyle and diet on the pH of the blood, I have learned that the human body is alkaline by design and acidic in all of its functions. If one can maintain the delicate alkaline pH balance of all the body fluids bathing every cell from within and from without at 7.365 then life will continue without pain, suffering, sickness or disease.

Louis Pasteur’s germ theory has become a curse. Antoine BeChamp an adversary to Pasteur and his germ theory for scientific fraud said this about the germ theory, “there is nothing so false that does not contain some element of truth, and so it is with the germ theory.” The germ theory is the controlling medical idea for the world. In Pasteur’s day, and ever since, other proposed theories about the cause of disease have fallen on death ear because they have tended to contradict that paradigm. NO matter how simple and logical an idea about the cause of disease, if it does not promote the concept of invasion of a germ or virus and their specific cures it does not fit into the medical paradigm.

More importantly, the germ or virus theory has become a curse because it has encouraged individuals to give up responsibility for their own health over to the medical community. If germs or a virus causes disease it stands to reason that control belongs to the medical community whose tireless researchers spend trillions of our money to find the right pill or potion to annihilate disease-causing germs or viruses.

This quest to cure disease through medication is at the heart of modern allopathic medicine and the multi-trillion dollar pharmaceutical industry. It is a quest that persists despite evidence indicating that airborne germs or a virus do not cause the disease for which they are credited.
After more than a century of trying, the Pasteurian germ theory and the virus theory has utterly failed in the quest to a cure for any disease. All major degenerative diseases are on the increase, as are so called infectious diseases which are not infectious at all! Every year, old symptoms are given new names – names like MS for polio, HIV/AIDS and SARS for poor sanitation, poor nutrition, poor lifestyle choices and drug use, Epstein-Barr virus for connective tissue disorders like fibramyalgia and NOW Ebola is back in the news killing thousands. This type of quack journalism is done to appear to be the work of a germ or virus. Unless we turn this nonsense around, the human race could become extinct like the dinosaurs from the treatments of modern medicine to kill a non- threatening or phantom germ or virus.

So What is a Virus? Read, like and share the following article:http://articlesofhealth.blogspot.com/2014/08/so-what-is-virus.html

So What Is A Virus?

A Micrograph of a poisonous acid crystal or Viral crystal in the live blood of a Cancer Patient

After 25 years of research, studying the affects of lifestyle and diet on the pH of the blood, I have learned that the human body is alkaline by design and acidic in all of its functions. If one can maintain the delicate alkaline pH balance of all the body fluids bathing every cell from within and from without at 7.365 then life will continue without pain, suffering, sickness or disease.

Louis Pasteur’s germ theory has become a curse. Antoine BeChamp an adversary to Pasteur and his germ theory for scientific fraud said this about the germ theory, “there is nothing so false that does not contain some element of truth, and so it is with the germ theory.” The germ theory is the controlling medical idea for the world. In Pasteur’s day, and ever since, other proposed theories about the cause of disease have fallen on death ear because they have tended to contradict that paradigm. NO matter how simple and logical an idea about the cause of disease, if it does not promote the concept of invasion of a germ or virus and their specific cures it does not fit into the medical paradigm.

More importantly, the germ or virus theory has become a curse because it has encouraged individuals to give up responsibility for their own health over to the medical community. If germs or a virus causes disease it stands to reason that control belongs to the medical community whose tireless researchers spend trillions of our money to find the right pill or potion to annihilate disease-causing germs or viruses.

This quest to cure disease through medication is at the heart of modern allopathic medicine and the multi-trillion dollar pharmaceutical industry. It is a quest that persists despite evidence indicating that airborne germs or a virus do not cause the disease for which they are credited.
After more than a century of trying, the Pasteurian germ theory and the virus theory has utterly failed in the quest to a cure for any disease. All major degenerative diseases are on the increase, as are so called infectious diseases which are not infectious at all! Every year, old symptoms are given new names – names like MS for polio, HIV/AIDS and SARS for poor sanitation, poor nutrition, poor lifestyle choices and drug use, Epstein-Barr virus for connective tissue disorders like fibramyalgia and NOW Ebola is back in the news killing thousands.   This type of quack journalism is done to appear to be the work of a germ or virus. Unless we turn this nonsense around, the human race could become extinct like the dinosaurs from the treatments of modern medicine to kill a non- threatening or phantom germ or virus.

What is a germ?
According to traditional medical microbiology a germ is a foriegn entity, such as a bacteria, yeast or mold that invades the body from the outside world and causes disease by attacking body cells.  I have suggested for years that germs are nothing more than biological transformations of body cells that have been compromised from an acidic lifestyle and/or diet.  In other words germs do not invade cells or attack cells they are born out of cells as a product of fermentation or spoiling.  Germs are like the smoke or ash of the fire.  They are the symptoms or the effects and NOT the cause of the cellular breakdown.
So What is a virus?
According to my research a virus is a liquid poisonous dietary and/or metabolic
acid. It is NOT a germ or a non-living entity that attacks the DNA of a cell as suggested by current medical savants.!

You do not catch a virus. Viruses are not sexually transmitted. The virus is an acidic waste product a poison created from an inverted way of living, eating and thinking.

From Webster’s New Twentieth Century Dictionary,
1975

virus, n.[L., poison.]

1. venom, as of a snake
2. (a) any of a group of ultramicroscopic
or submicroscopic infective agents that cause
various diseases, as smallpox: viruses are
capable of multiplying in connection with living
cells and are variously regarded as living
organisms and as complex proteins;
(b) specifically, a filterable virus;
(c) the exudation from the vesicles of cowpox,
used as vaccine for smallpox.
3. that which corrupts or poisons the mind
or character; evil or harmful influence.

From Oxford English Dictionary

Virus [L virus slimy liquid, poison, offensive odour or taste. Hence also F.,
Sp. Pg. virus.]

In Lanfranc’s Cirurgie (c 1400)77 the word explained as ‘ a thin venomy quitter’ is merely taken over from the Latin text.

1. Venom, such as is emitted by a
poisonous animal.
(dated quotations)
2. Path. A morbid principle or poisonous
substance produced in the body as the result
of some disease, esp. one capable of being
introduced into other persons or animals by
inoculation or otherwise and of developing
the same disease in them.
(dated quotations)
3. fig. A moral or intellectual poison,
or poisonous influence.
(dated quotations)
4. Violent animosity; virulence.
(one dated quotation)

From The Encyclopedia Americana, 1958

Virus, Infectious disease-producing agent largely characterized by small size and
ability to reproduce only within living cells, that is a minute, obligate parasite.

The discovery of the chemical nature and crystallization of tobacco mosaic virus (the
first virus or crystallized acid discovered) by Wendell M Stanley in 1935 (Science, June 28, 1935) opened the way for purification and intensive study of viruses or crystal acids.

Dr. Stanley brought a german scientist Dr. Peter Duesberg to Stanley Hall in Berkeley University in the 1960s. Dr. Duesberg wrote the book, Inventing the AIDS Virus where he suggests that HIV, Hep C. Hunta Virus and Ebola virus are ALL phantom viruses.

Now, to get our heads on straight concerining germs and the virus,
here is a piece from “The Blood and Its Third Anatomical Element” by Antoine Bechamp, a French Physician and Medical Researcher.

Pages 210-211.

“An eminent surgeon, M. Verneuil, ended by admitting as a demonstrated theorem that there
is no spontaneous tetanus, that there is no spontaneous small pox, syphilis, glanders,
hydrophobia, tuberculosis, carbon or malignant pustule; declaring that the pathogenic problem consisted solely in discovering how and when the microbe, also called virus, come from without, penetrates into the organism; declaring that the question is thus stated between old medicine and the microbina medicine with extreme simplicity and without the least ambiguity.”

“But these assertions (of Surgeon Verneuil) are reduced to nothing, when we call to mind that
the pretended germs of the air are only the microzymas of organisms which have disappeared,
which had become bacteria by evolution; that even at the Acadamy of Medicine I said–and no
one ventured to contradict me on the nosological roll by taking the pretended pathogenic microbe
in normal air, but only in the diseased animal.”

I must say that I am indebted to both Dr. Antione Bechamp and Dr. Verneuil for saving ourselves
and whatever is left of our civilization from the peril of a viral microbe dogma and from
current vival medical treatments, for those who have ears to hear and eyes to see.

Bottom line, the present of a virus or a crystal acid or a bacterium such as TB or the latest invention of a SARS like virus known as the Novel Coronavirus which todate is responsible for the death of 12 people is not caused by the infection of a germ or virus, but is caused by personal acidic lifestyle and dietary choices.

If we want to find the cure for disease we need only to look at our dietary and lifestyle choices. If you heed the ignored, even rejected discoveries of Pasteur’s peers and scientists of the 19th and 20th century, adding those to my own discoveries, you will learn the true cause of disease.
Until the medical community starts looking at causes rather than devoting its time looking for cures, and until we start taking responsibility for our own lifestyle and dietary choices, I believe the human race is in trouble of becoming extinct.

Dr. Benjamin Rush, Physician and signer of the Declaration of Independence, 1776 said this: “Unless we put medical freedom into the Constitution, the time will come when medicine will organize itself into an undercover dictatorship, To restrict the art of healing to one class of men and deny equal privileges to others will constitute the bastille of medical science. All such laws are un-American and despotic.”

Where does life begin? In the womb or the grail, the holy grail, in the amniotic fluid, in a 98.6 F, one percent water and salt solution or 1 part salt to 100 parts water. This solution is called the sol. This natural salt solution, called “sol” is from the origin of the word, directly connected to the word “soul”. What we call “sol” for our salt solution (a solution of two in one- no more polarity), was believed by the ancient Celtics to represent our soul, as the soul originated, in their belief, from the ocean where we are all born from the same fluids, arising from the same “sol” a solution of salt and water.

Our body in its wholeness is an ingenious creation of nature, It has been given all mechanisms to not only sustain its life but also to create new life. Every healthy person has innate regulatory mechanisms to maintain its alkaline design and self-healing powers, which ensure or reestablish the natural balance of the bodily functions, the homeostasis. It is not the doctor that heals us, nor the medication, but our own innate alkaline regulatory mechanisms. Our body is able to fully regenerate itself. Therefore, it is advised to use great discernment before labeling any disease as “incurable” or “untreatable.” If doctors come to the conclusion that a disease is incurable, they would be more accurate in saying that with their knowledge and experience, they are not able to offer any further help. The word “incurable” conveys fear, or false evidence appearing real, which stifles and weakens our body’s innate alkaline mechanism.

Bio-chemically speaking Health is all about alkaline balance. Bio-energetically speaking Health is all about energy. Vibrating energy is the origin of matter and the origin of life. And matter is nothing more than organized energy.

In 1984, the Swiss physicist Dr. Carlos Rubbia, received the Nobel prize for discovering a mathematically calculable natural constant with which he could calculate the ratio of mass particles (matter) in relation to navigating energy particles, The ratio of matter to energy that forms matter is 1 to 9,746 to the power of 108 or about 1 to 1,000,000,000 which means it takes one billion energy units to create one single unit of matter in a materialized tangible form. Isn’t interesting that we for the most part, preoccupy ourselves with only 1 billionth part of reality: that which is in a material form and can be seen and touched. We fail to see the far greater amount of energy particles it took to materialize our reality. This revolutionary scientific discovery shows us clearly that every form of matter is subject to higher energetic interactions and subject to change of form and function.

When we analyze the energy content of any form of matter, we arrive at its smallest part, the atom and its protons, electrons and neutrons. There is ongoing movement without any contact- nothing tangible, just pure vibrating energy. This vibrating energy creates a frequency, which can be measured, a so-called wave length which can be seen using my photon interference photography. Every form of matter is characterized as a specific frequency spectrum. And each frequency spectrum can be measured using a decibel meter. All organized matter is nothing more than organized energy that gives off a specific frequency and a specific sound which can be measured and heard. When we turn on a light or an electrical device we can see the energy but we cannot perceive the electrical current itself, but we except its existence. This same materially non-perceivable electricity, this energy, flows through our body fluids especially our blood. Every one of us has enough measurable electrical current flowing through us to light up a 100 watt light bulb.

Life/light = energy and energy = information or intelligence.


Everything that exists not only exists as energy but also as a carrier of information or intelligence, whether it is a human being, a form of food or drink, or a rock. Life is a constant exchange of energy and intelligence and the best place to view this life energy is in live and dried blood microscopy.

Plasma which is 92% alkaline water at a pH of 7.365 is a good example for showing how matter as energy is transformed when additional energy is added or subtracted. Water has three different distinct bodies or states: solid, liquid and gaseous. Ice is frozen water or like the thickening of the blood. We can see it and feel its coolness. By adding energy in the form of heat to the ice it transforms back into a liquid. When we add more energy to the water it begins to boil and the molecules start moving faster and faster that they begin to transform into steam and become gaseous. This transformation of organized energy as matter from one form to another is know as biological or energetical transformation or also referred to as pleomorphism.

Energy and intelligence are identical.
Every form of energy has a specific wavelength
Every wavelength has its individual content of intelligence
There are no accidents in the order of Nature


Meanwhile, we know of about 40,000 different diseases and the list is growing that are treated by the 1,200 different allopathic specialty fields with 58,000 different kinds of allopathic preparations or medicines. However, the word diseases in the plural form, is not a accurate. Have you ever heard of “healths”? We are either healthy or ill. This illness signals a lack of energy and shows up in the form of a symptom. To represent a symptom as an illness is technically and scientifically inaccurate. The symptom is merely the intelligent cry of the energetically defective and suffering body, crying out for help. And normally, the body turns to a weakened organ to give us a hint, through a symptom, that things are not in order.

Our bodies either hum or honk

Upset stomachs or high blood pressure or high blood sugars is the body honking. The honks of our bodies are telling us there is a state of pH or energetic imbalance.
Why does pH balance or pH Homeostasis define good health?
pH balance or pH homeostasis in humans commonly refers to the internal balance of the body’s electro-magnetic and chemical systems in response to the changing conditions of the external world and the changing conditions of the internal world. The word homeostasis comes from the Greek words: “homeo” means similar or “alki” or “alkaline” and “stasis” means a tendency toward maintaining stability. There are many homoeostatic mechanisms in our bodies that help maintain this balance and our state of health is directly related to the health of these mechanisms. pH homeostasis is maintained by dynamic processes of feedback and regulation. pH homeostasis has only one objective: to preserve the beneficial conditions of life in the internal alkali environment. Every day we are bombarded with external influences that threaten that balanced internal alkaline pH environment. Some of these threats include becoming too hot or too cold, eating too much or eating acidic foods or drinks, breathing polluted air and being exposed to chemicals over a period of time, whether they be recreational or prescribed by our Doctor.

Our cells, especially the red blood cells can only survive when our bodies are strong enough to maintain pH homeostasis at 7.365 or to regain it quickly after we have been exposed to toxic environmental threats. Some of the pH homoeostatic mechanisms in the body include temperature regulation, dilation of the eye, blood composition, heart rate, blood pressure, water content, blood sugar level, mineral relationships, and of course the acid/alkaline balance of our body fluids.

An essential feature of these mechanisms is that they enable the red blood cells, the tissue which is a product of the red blood cells and the whole of the organism, also a product of blood, to adapt to changes in both internal and external environmental conditions. If the pH homoeostatic mechanisms are impaired the body loses its ability to regulate these mechanisms.
By looking at living blood using a compound phase contrast microscope I can view the quality of the red blood cell, its environment and how well the body is managing these pH homoeostatic mechanisms. The interdependence and close coordination of the many bodily functions, which work so well when we are in alkaline balance or health, may be upset by a chain reaction when any part of the system breaks down from metabolic acids which have not been properly eliminated through, respiration, perspiration, defecation or urination. If this chain reaction is too drastic, the red blood cells and body cells will become acidic and begin to biologically transform into other cellular forms – like bacteria or yeast.

The normal state of health is not a static condition, but a coordination response of many systems and mechanisms. Fluctuations occur within a very narrow pH range. An imbalance of a point or two on the acid/alkaline pH scale is extremely disruptive to health. A few percentiles of variation of oxygen concentration in the blood can impair function. In the bloodstream, the slightest changes can be observed in the structures of the red and white blood cells, the level of cellular debris, the creation of cholesterol or calcium crystals, etc. If the blood sugar content is continually elevated due to body cell transformation or breakdown, the body chemistry becomes upset. An infinitesimal deficiency of sodium, calcium, potassium or magnesium, the alkaline buffers of the body can cause a problem in the function of many body parts.

We must keep our pH homoeostatic mechanism strong so that we can deal effectively with our world. If we are humming and the process of pH homeostasis is orderly, life continues; if we are honking and pH homeostasis is continually being disrupted, our health is in jeopardy.
pH Homeostasis is a bit like balancing the books in accounting. It si maintained by balancing inputs with outputs – alkalinity in acids out.

How well we adapt in health and sickness is largely a function of the pH homoeostatic mechanism. The body’s chemistry response to such subtle changes that a negative thought, an acidic food or drink, or eating too much food can be a problem for maintaining alkaline balance.

In 1988 an article of the New England Journal of Medicine stated that, “most major chronic disease probably results from the accumulation of environmental factors over time in genetically susceptible people.”

In 1965, Rene Dubos, a medical historian and philosopher, pointed out that the body is imperfect in its attempts to adapt and maintain pH homeostasis. She said, “the mechanisms involved in regulating homeostasis do not always return the body’s functions to their original state. They can be misdirected. The body only has the ability to adapt to insults for so long. When it can no longer adapt, inflammation and then degeneration sets in. Health is the state that the body attains when an individual responds adaptively and restores the body to its original integrity.”

The term “homeostasis” was coined in the mid-1920’s by the American physiologist, Walter B. Cannon. But he was building on a concept of balance that dated back to ancient Western, Eastern, and Middle Eastern civilizations.

The balance equals good health equation was first suggested by Hippocrates (460-375 BC) and the ancient Greeks. Hippocrates considered health to be a state of harmonious balance and disease a state of disharmony. He and his contemporaries believed that harmony and balance existed between organs, between bodily fluids, and between body and soul. When the body is out of harmony and balance, illness occurs.

Hippocrates studied the entire patient in his or her environment, noting the effects of climate, food, and occupation on health. “Our natures are the physicians of our diseases, ” he said, describing the healing forces we all have within us as the healing power of Nature. It was the physician’s objective to restore harmony with food, exercise, rest, and with medicinal remedies designed to remove the harmful acidic excesses. This conservative approach was designed to let nature do the healing and above all, as Hippocrates said, “to first do no harm.”

The Greeks ideas on equilibrium and health evolved further under the philosopher Aristotle (384-322 BC). He felt that a healthy body worked through what he described as a hemostat, a device that returns the body to a state of equilibrium even when it is subjected to stimuli that disturbs this balance. Everything is tied to this state of equilibrium, including the psyche and emotions, and nothing could be regarded as a separate component. To lead a healthy life, the condition of balance had to be maintained, This could only be achieved if the body had an adequate feedback system, a means by which signals were transmitted to different parts of the body to help move it back into balance when it moved too far off alkaline center.

This psychological viewpoint was shared by another philosopher, Epicurus (341-270 BC). In his writing he referred to psychological stress and suggested that an individual’s quality of life could be improved by coping with what we would now describe as emotional stressors.

As early as about 120 AD in India, Eastern philosophers had reached similar ideas about the importance of balance in health. A general medical textbook from that time, the Caraks, described health as a balance of bodily elements know as dhatus, and a happy mental state called prasana.

The Middle Eastern approach incorporated the Hindu teachings with the Greco-Roman medical doctrine. Being base upon both religious and philosophical ideas, Islamic healing involved both body and soul.

Over 1000 years later, during the Middle Ages in Europe, good health was still linked to this notion of balanced physical, emotional, and spiritual state. To help people achieve this state, European hospitals were set up by religious orders and attached to abbeys, monasteries, and convents. Doctors prescribed diet, rest, sleep, exercise, and salt baths.

In 1600 Thomas Sydenham had begun classifying diseases, even though he believed disease was a result of imbalance, consistent with Hippocrates and Galen.

In 1628 Harvey traced the circulation of the blood, arguably perhaps the single greatest achievement in medicine.

In 1753 James Lind showed that Scurvy could be reversed with the limes that contain limonene – an antitoxic or antacid.

Doctors began to lose their way in 1796. In 1796 Benjamin Rush observed that all fevers were associated with flushed skin, he concluded that this was caused by distended capillaries and reasoned that the proximate cause of fever must be abnormal “convulsive action” in these vessels. He took this a step further and concluded that all fevers resulted from disturbances of capillaries and since the capillaries were part of the circulatory system, he concluded that a hypertension of the entire circulatory system was involved. Rush proposed to reduce this convulsive action by “depletion” or bleeding. A reminder that the medical establishment’s acceptance of bleeding exists today in the name of the British Journal “The Lancet” one of the leading medical journals in the world. Today bleeding is called phlebotomy.

Also, In 1796 Edward Jenner took the pus from the runny sores of sick cows and injected it into the blood of his “patients. He thought that since pus is seen routinely in all kinds of wounds, pus was seen as a necessary part of healing.

In 1788 vaccinia was the bacteria that medical science suggested caused cowpox.

In 1830 the development of the first modern day achromatic microscope.

In 1835, Harvard’s Jacob Bigelow argued in a major address that in “the unbiased opinion of most medical men of sound judgement and long experience . . . the amount of death and disaster in the world would be less, if all disease were left to itself.”

In 1840 Jacob Henle in his essay, “On Miasmata and Contagia” first formulated the modern germ theory. He suggested that disease seem to germinate, grow and spread – like a first point or origin, a seed, a bacterium. The germ theory said that minute living organism invade the body, multiply and cause disease and that a specific germ causes a specific disease.

In 1850 Samule Thomson said, ” May the time soon come when men and women will become their own priest, physicians and lawyers – when self-government, equal rights and moral philosophy will take the place of all popular crafts of every description . . False theory and hypothesis constitute nearly the whole art of medicine.”

In 1860 Louis Pasteur suggested that living organisms, not a chemical chain reaction caused fermentation, winning converts to the germ theory.

In 1881 an American scientist George Sternberg was the first to isolate the fungus, pneumococcus and the first to observe the white blood cells engulfing bacteria, a key to understanding the immune system.

In 1882 a German, Robert Koch isolated the tubercle bacillus and declared it as the bacterium that caused tuberculosis that further confirmed the germ theory of Pasteur.

In 1884, German scientist Friedrich Loeffler isolated the diphtheria bacillus from throats of patients, grew it on a special medium (labs today call this Loeffler’s serum slope to grow the bacteria from suspected cases), and began careful experiments in animals that took several years. His work suggested that the bacteria themselves did not kill; the danger came from a toxin, diptherium, an acidic poison that the bacteria excreted as a waste product from sugar metabolism.

In 1885 Max von Pettenkofer insisted that Koch’s bacteria were only one of many factors in the causation of disease. His dispute with Koch became increasingly bitter and passionate. Petterkofer determined to prove himself right, prepared test tubes thick with lethal cholera bacteria. Then he and several of his students drank them down. All survived. Petterkofer claimed victory that germs do not cause disease.

In 1889 Pasteur’s proteges, Emile Roux and Alexandre Yersin grew broth thick with diphtheria bacteria and used compressed air to force broth through a filter of unglazed porcelain. The filter was designed by Charles Chamberland, a physicist working with Pasteur; though only a tool, the filter itself would prove to be immensely important. NO bacteria or solids could pass through the porcelain. Only liquid could. They then sterilized this liquid. It still killed. That proved that bacteria, an insoluble could not kill, but a soluble, an acidic toxin did the KILLING.

The cure from diphtheria was not in killing the bacteria but neutralizing the acids or excretions from the bacteria.

In 1900 Frederick Gates an intellect and Baptist Minister and an assistant to John D. Rockefeller, saw an opportunity to exploit the medical field because of its admitted uncertainty and ignorance of the time. He had organized many business ventures for the Rockfellers’ and convinced John D Rockefeller to open the Rockefeller Institute for Medical Research. The Rockefeller Institute saw medicine itself as its field from its earliest existence scientists studying disease based upon the germ theory of Pasteur.

In 1901, William Henry Welch was hired by John D. Rockefeller to set up the Rockefeller Institute for Medical Research. William Henry Welch was steeped in the germ theory and established its strong hold on the medical model. You might call Dr. Welch the Father of American Medicine and the perpetrator of the Pasteurian Germ Theory.

After the civil war medicine had discovered drugs – such as quinine, digitalis and opium of which Oliver Wendell Homes the physician Father of the Supreme Court justice said, “I firmly believe that if the whole materia medica, as now used, could be sunk to the bottom fo the sea, it would be all the better for mankind – and all the worse for the fishes.”

In 1911, the head of the school training French army doctors in public health said that germs alone were “powerless to create an epidemic.” But it was too late, this particular view was now considered simply a minority opinion. The germ theory now had its hold on the governments of the world!

In 1911, the medical establishments made up a story that Peyton Rous discovered a bacteria that caused cancer and received a Noble Prize for his discovery posthumous in 1966. This gave rise to the term virus named after Peyton Rous’s bacteria. Peyton Rous never suggested this in any of his research that his bacteria caused disease let alone cancer. This story gave rise to a new group of bacteria called filterable bacteria that the medical community now refers to as virus – beginning 1996. There is NO scientific evidence that shows that virus’s have ever caused ANY disease that would also include are newest phantom virus – the Novel Coronavirus.

These ideas of balance were some distance from those of earlier societies that ascribed illness to the supernatural powers they believed governed their lives. The Babylonians, the Egyptians, the ancient Americans saw disease as an entity unto itself, a potent demon that struggled to dominate, attacked, penetrated, and possibly even kill its unfortunate host.

Offend the Gods, an ancestor, or an evil witch and be struck down as punishment. Lead a sinful life and you were tempting fate.

Of course, we perceive that these ideas about disease are no longer widely believed, which makes it all more the ironic that Pasteur’s germ theory has had and still has a stranglehold on 19th, 20th and now 21st century medicine. As medical writer Alberto Seguin described in an article entitled, “The Concept of Disease,” the demonic idea of disease reached its full height with the germ theory. It became possible to bring together rational and scientific thought with irrational tendency to personalize disease. The germ in what ever name it is called, West Nile Virus, Ebola, Hunta, HIV, Anthrax, AVIAN< SARS and now the Novel Coronavirus, are the scientific demon, the curse, the lie and the fraud that is said to attack and kill!

If we will consider disease as a symptom of disease not the cause, then the germ is nothing more than an expression of acid/alkaline fluid imbalance and a biological transformation of blood and body cells of what use to be organized to that which is changing into a new form. This was my discovery in 1994. I witnessed biological transformation as seen on pg. 126 of my book “Sick and Tired” the transformation of a rod bacteria back into a red blood cell and then back into a bacterial rod. I knew for the first time that bacteria was not a demon, not an entity but a biological transformation, a new formation of a preceding form. Not the cause of disease but the expression of a change in the internal environment which had given rise to change. For several years I felt alone in this discovery until I learned of the works of the giants that proceeded me that had their finger on the magic of life.

Claude Bernard (1813-1878) “The terrain is everything the germ is nothing.” And upon the death bed of Louis Pasteur admitting to Claude Bernard that he was right in 1895.

Antoine BeChamp (1816-1908) “Disease is born in us and from us.”

Florence Nightingale – a famous nurse (1820 -1910)

Mathias Schleiden and Theodor Schwann (1839)

Gunther Enderlein ((1872- 1968)

Walter B. Cannon (1871-1945) “Only by understanding the wisdom of the body shall we attain the mastery of disease and pain that will enable us to relieve the burden of the people.”

Royal Raymond Rife (1888-1971)

Wilhelm Reich (1897 – 1957)

Gaston Naessans (1924-2005)

Philosophically speaking, Pasteur had an ally in Napoleon III, who came to power in 1852. The Emperor believed in a police state and in using complete control to rule. Pasteur’s mechanistic idea of disease, finding the right cure for each germ, fit into this philosophy of control.

Giving the responsibility to the any government to cure disease is giving up control and our personal freedom. It takes responsibility – and power – away from the individual. In the words of Antoine BeChamp, “there is nothing so false that does not contain some element of truth and so it is with the germ theory.”

One of five of us will become diabetic
One of two of us will develop cancer
One of two of us will develop cardiovascular disease
One of six couples will suffer from unexplained infertility.
One of seven women in the US will develop breast cancer.

We need to get out of the disease business. If we want to understand health, energy and vitality then we need to study the people who are healthy. Over the last 25 years I have been studying health and how it relates to the blood, the diet and our personal lifestyle choices. Viewing live and dried blood under a pHase contrast microscope is the pinnacle of understanding health and how to achieve health with alkaline foods, drinks, exercise, breathing, getting adequate rest, etc.

Now, it is my hope that we will all soon realize that we are all responsible for our own health – you alone. A medical practitioner can only help to relieve symptoms. Ultimately, you are the one who has to take charge. Health is a choice just as disease is a choice. You are responsible for what goes into your mouth and what comes out of your mouth, as well as for what you think, feel and do. Health is all about personal choices and consequences.

The health and energy of the human organism is the knowledge that our bodies are alkaline by design and acidic by function. I have found that the best way to maintain that alkaline design is through an alkaline lifestyle and diet, I call the pH Miracle which is outlined in our books, The pH Miracle, The pH Miracle for Diabetes, The pH Miracle for Weight Loss and NOW the pH Miracle for Cancer.

Finally, the quality and quantity of ones life is a personal choice with personal consequences. One can choose daily health, fitness and life by living in a way that maintains the alkaline design of the body fluids and cells or one can choose an acidic lifestyle and diet and reap the consequences of pain, sickness, disease and death.  Blaming a germ or a virus for the cause of disease and death,  including our newest so-called virus the Novel Coronavirus, responsible for 12 deaths worldwide, is just an excuse or a scapegoat for keeping the medical myth alive that ‘germs cause disease’ and for a person NOT taking responsibility for personal acidic lifestyle and dietary choices which is the true cause of disease and death. 
May you choose the consequences of your life wisely! I believe it is a matter of life and death.
To learn more about the pH Miracle lifestyle read The pH Miracle Revised and Updated by Dr Robert and Shelley Young.
Become part of our healthy alkaline community? For more information go to: www.phmiracle.com