White Blood Cells

White Blood Cells

We are told white blood cells are claimed to be responsible for fighting off "invaders", which we know now that paradigm is theoretical and is nothing more if not less.

Pleomorphism and germ theory

The accepted biological paradigm today, which has led to the development of the pleomorphism and germ theory, is Monomorphism (Gr. mónos: single + morphē: form).

This paradigm, developed by Louis Pasteur and other scientists, states that all microorganisms only have one possible form and do not have the ability to evolve into different types of organisms.

The germ theory followed, which states that specific diseases are caused by infection with specific microorganisms and are cured when the microorganisms have been destroyed.

Pleomorphism, the polar opposite of Monomorphism, was developed by scientists like Antoine Béchamp and Günther Enderlein and states that microorganisms have various life cycles and stages of development that can range between viruses, bacteria, yeast and fungi, depending on the type of microorganism and the environment it is presented with.

Antoine Béchamp

Pleomorphism and the Germ Theory Explained

We will begin our overview of the history of pleomorphism at the beginning, with French scientist Antoine Béchamp (1816-1908).

Béchamp was a Master of Pharmacy, Doctor of Science, Doctor of Medicine, Professor of Medical Chemistry and Pharmacy, Fellow and Professor of Physics and Toxicology, Professor of Biological Chemistry and Dean of the Faculty of Medicine.

He was actively involved in his biological research at the same time as Louis Pasteur.

Ten years of experimentation led Béchamp to the conclusion that the tiny “molecular granulations” that have been observed in the cells of plants and animals by other researchers, were living elements.

He called them “microzymas” (small ferments), due to their ability to ferment sugar.

He continued his research over another 13 years, developing the Theory of Microzymas. This theory states that the microzyma is an independently living element, found in all living organisms and survives after the death of the organism. It functions to both build and recycle the organism.

It is the builder and destroyer of cells; it precedes life at the cellular level and is the foundation of all biological organization. In healthy conditions, the microzymas have a beneficial relationship with the organism and fermentation occurs normally.

However, microzymas are very sensitive to biological signals, responding to changes in the terrain, especially pH. When the terrain becomes compromised, the microzymas become what Béchamp called “morbidly evolved”, changing into microscopic forms (bacteria) that contribute to the development of illness. Béchamp believed this characteristic to be linked to the function of the microzymas to recycle the body upon death.

The change in the terrain is interpreted by the microzymas that the organism is already dead, which is a signal for them to change into the “morbidly evolved” forms capable of more vigorous fermentative breakdown.

Béchamp was also able to show that compounds such as alcohol and acetic acid are produced in the tissues of all organisms as a direct result of the fermentation activity of the microzymas.

The difference between the two theories is quite clear:

Pasteur’s germ theory sees disease as being caused by external factors, whilst Béchamp’s pleomorphic theory considers the internal environment as the most important contributing factor.

Béchamp did not deny that the air carried germs, but maintained that they were not primarily responsible, and certainly not necessary, for disease. They are only present because of the compromised terrain. A good analogy was made by Rudolph Virchow: “… mosquitoes seek the stagnant water, but do not cause the pool to become stagnant.”

Claude Bernard

A researcher worth mentioning, who preceded Antoine Béchamp, was French physiologist Claude Bernard (1813-1878).

He was one of the first scientists of his time to see that disease is not simply determined by the germs involved or the symptoms present. He believed disease to be a general, underlying condition, affected and determined by the body’s internal environment, which he called the “Terrain”.

The state of the terrain is determined by four factors, namely:

1) its acid/alkaline balance;

2) its electric/magnetic charge;

3) its level of poisoning;

4) its nutritional status.

Royal Raymond Rife

During the 1920’s R.R. Rife was researching a method to treat disease by destroying microorganisms through radio frequency radiation. To help him determine the correct frequency, he designed and built a most incredible microscope (consisting of 5682 parts) that used polarizing prisms to “stain” the organisms with light. He then used a radio frequency beam ray to destroy the organisms, which he used successfully to cure many serious conditions, including polio, TB and cancer.

He is relevant to the history of pleomorphism in that he was able to isolate a virus he found in cancerous tissue and transform it into a fungus and then into a bacterium. He was able to repeat this hundreds of times and showed that the pleomorphic development of microorganisms goes beyond the bacterial level to the fungal stage.

Günther Enderlein

German zoologist and bacteriologist Prof. Dr. Günther Enderlein (1872-1968) is still considered by many as the father of pleomorphism. He based his work on that of Antoine Béchamp and conducted research for over 60 years, which led him to several remarkable discoveries.

He showed that the protit, not the cell, is the smallest biological unit of life. Protits (Béchamp’s microzymas) are small, living protein particles found in all the cells, blood and other fluids of all living organisms. They can not be destroyed and survives after the death of the organism, performing the function of decomposition.

Much of his discoveries he made because he was looking at live blood in darkfield. This helped him to see that in healthy conditions the protits remain small and beneficial, working with the body in a symbiotic relationship. However, when presented with a disturbed environment, the protits are able to develop into more complex, pathogenic forms, including bacteria and fungi. The specific symptoms and forms of disease depend on the level of development of the pathogenic forms, which is governed by the state of the terrain.

Enderlein referred to all the possible developmental forms of the protits as the Endobiont. He discovered that two microbes exist, and has always existed, in all vertebrate mammals. These are Mucor racemosus Fresen, which he called the primary parasite, and Aspergillus niger van Tieghem.

Mucor is found in the blood and other cells and when in its beneficial, primitive stages, it is responsible for the coagulation of blood. When in its pathogenic stages, Mucor leads to congestion, cancer and many other degenerative diseases.

Aspergillus, in its primitive stages, is responsible for the regulation of the citric acid cycle and calcium metabolism.

Enderlein believed that the infection of mammals with Aspergillus allowed for the development of skeletal structures.

Aspergillus can be found in the bones, connective tissue and lymphatics. Pathogenic phases of Aspergillus are responsible for para-tubercular diseases, connective tissue disorders, arthritis and skin problems.

Enderlein showed that while exogenous microorganisms are monomorphic and produce recognizable, communicable diseases, other non-communicable, chronic diseases are caused by the pathogenic evolution of the pleomorphic Endobiont.

This evolution is governed by the state of the terrain, particularly the pH.

The Anartatic Law of Interdependence states that the progressive development of microorganisms from the protit stages into their higher and highest stages requires a progressively descending pH.

This process, once started, is then supported by the Endobiont itself, which produces acid wastes from its metabolism of protein. Each microorganism produces a specific organic acid: Aspergillus produces citric acid and Mucor produces lactic acid.

It is important to note that Enderlein described the evolution of Mucor and Aspergillus, both of which find their culminant (highest stage of development) as a fungal organism.

Other organisms that may also be pleomorphic do not necessarily have their culminants in the fungal phase, but rather in the bacterial phase (e.g. Staphylococcus aureus).

Gaston Naessens

Quebec scientist Gaston Naessens, who is currently involved in research, has also contributed greatly to pleomorphism. He designed a special microscope, called the “Somatoscope”, which enables him to observe changes in living tissue at very high magnification and resolution.

He, like Enderlein and Béchamp, discovered small living particles, which he called “somatids”. He has identified two somatid cycles: the microcycle and the macrocycle. Only the microcycle occurs in health and consists of only three stages, where all three forms are symbiotic. The macrocycle occurs in disease and consists of sixteen stages, including bacteria-like and fungus-like forms.

The culminant fungal phases of Mucor racemosus and Aspergillus niger only occupy the blood after death as it requires an acidic environment.

There are transitional mycelial phases that can however be observed in the blood.

These phases represent the highest phase of Mucor’s development in the living host and their presence is indicative of severe conditions.

https://livebloodonline.com/pleomorphism-and-germ-theory.../

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White Blood cells

FUCNTION OF WHITE BLOOD CELLS - ROBBERT YOUNG -

When white blood cells help TO:

- maintain fluid purity and alkalinity.

-to mobilize in order to collect bacteria and yeast

-an important cell function that helps mediate

- bacteria and yeast

IF POISONED , can then cause:

- increased acidic cellular debris in the body fluids causing blood and lymphatic congestion leading to:

- poor circulation, light headedness, dizziness,

If suppressed regularly:

-may lead to more serious acidic symptomologies

-ulceration and degeneration of the tissues

-degeneration of organs leading to heart dis-ease and cancerous conditions.”

White Bood Cells:

mediate bacteria and yeast and, at the same time, increases levels

of exotoxins and myctotoxins (acidic waste products from

bacteria and yeast) that promote the biological

transformation of healthy body cells and tissues.

https://phoreveryoung.wordpress.com/.../the-acid.../...

_Nature Article on Pleomorphism-

"...White blood cells are a part of the pleomorphic cycle..."

"Structures representing cellular debris possibly originating from white blood cells were also observed (yellow arrow in C). Scale bars: 8 μm." "Enderlein described small entities called and in human blood and believed that these particles underwent a complex life cycle that correlated with disease progression " ----"

"...pleomorphic bacteria exist in the blood of healthy humans."

just wanted to point something out

" blood of healthy and diseased individuals appeared to be continually infected with bacteria. Naessens described small living blood particles, which he called , as part of a complex life cycle that may culminate in the formation of (change out the word pathogenetic with the word routing or signaling or communicate - exchangeable) - pathogenic bacterial forms under disease conditions"

"In order to confirm the presence of these proteins within blood particles, we performed fluorescence microscopy using antibodies that react against HSA, HSF, or Apo-A1, followed by washing steps. Our observations indicated the presence of the three blood proteins in the particles (Fig. 6H–J).

An antibody that recognizes heat-shock protein 70 (Hsp70), which was absent in the proteomics analysis of the particles (Supplementary Table 2), was used as a negative control (Fig. 6G). Co-localization of HSA and HSF was also observed within the particles (Fig. 6K).

These results suggest that the refringent particles observed in human blood actually represent protein aggregates derived from blood. "

"Structures representing cellular debris possibly originating from white blood cells were also observed " -

https://www.nature.com/articles/s41598-017-10479-8...

FROM WHAT I UNDERSTAND FROM THIS - "ANTIBODIES" ARE REALLY JUST MICROZYMAS (SOMATIDES/ PROTITS )

Blood microzymas

There exists, in fact, in the blood of all the animals that we have examined…, an

innumerable number of mobile molecular granulations, having all the characteristics of

microzymas…

But, you understand it well now: for the observation to be conclusive, it must relate to the

blood when it leaves the vessels, before the formation of the clot, that is to say before they do.

were used to form fibrin and especially on blood that we know to give little of this substance;

the blood of very young animals is in this case ...

In the middle of the globules, we always see a crowd of microzymas. They are quite similar to

those of the liver, but smaller and more transparent. It was their thinness and transparency

that prevented histologists from seeing them. In addition, because of their small size, it is useful

to use the immersion objective, No. 7 from Nachet. … In the blood defibrinated by the beating,

almost all of the microzymas have disappeared. They are difficult to see in mixed blood. But

after their action on starch or sugar water and their development in strings of 2 to 20 grains,

they are positively insoluble ...

Blood, contrary to popular belief, therefore does not contain only two histological forms:

microzymas are the third organized element of blood.

But do blood cells contain microzymas? We answered yes, Mr. Estor and I.

MICROZIMAS PDF

https://l.facebook.com/l.php...]-R&c[0]=AT0zKnw3jkpqgpMIQyOssbOV-nBzTfAv1BfQ63My71zGsXXSP-a63T7gy7gOanBYgFHiwQEweSpqT8OPMLWVu-fWGkoGQQArqOcRKTpsoIABFAuOyjrFmWsqjjH3s96Pg6hrLTL8Er3HfbP9gDV-iwtIB6XGDXg2H_7336viwj4f_Pgi

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The sheer boundless polymorphism of the phenomenological forms of the

cyclogenetischen constructive series of Protit, Chondrit, Mychit, bacterial rod,

Cystite, Thecit, composite Thecit (Synthecit) with Guarneri's corpuscles and mold

spores (conidia) up to the cell-like forms Chlamydozoit, Morulit and Amoebit, can

only be understood through the constant boundlessly potentiated (by means of

concentration and conjugation) valency of the nuclear elements (Mych, Symmycha)

of the ascending Dynamogenie. One should keep in mind that the haploid and

diploid phase of plant and animal, a form - here initially fixed as to number, size

and arrangement - of the final nuclear elements, is only a meager remnant of the

boundless primordial bounty of the Dynamogenie of the proto-organisms, which

is represented by the series Chondrit, bacterium, mold. C. Börner, in his

fundamental tocontology (whose design significance for all these organisms is

quite well known to all biologists) has described

(Die natürliche Schöpfungsgeschichte als Tokontologie [The natural history of creation as

tocontology] Leipzig, Th. Weicher, 1913, 159 pgs., 10 tables & 11 illus.)

what gigantic dimensions of differentiation within this simple alternation alone,

between merely two nuclear valencies - namely from haploid to diploid phase -

still remain for plants and animals.

The reason why the homogeneous proto-granule (Protit and Symprotit) has not

yet been taken seriously, and why the necessary genetic evaluation has not been

made, is that people have not been able to tear themselves away from the

centuries-old, firmly rooted idea that the cell is the lowest fundamental unit of

life.