Fungus by Coyle

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FUNGUS

The species specific understanding of, and difference between bacterial

phase and fungal phase developments in blood pictures.

©Copyright 1997 by Coyle, Petaluma, California, USA

(Explore Issue: Volume 8, Number 3)

Diseases of the skin, digestive organs, urogenitary tract, mouth, etc. are

caused by the multiplication and spread of fungal microorganisms known as

mycelia. Mycoses (fungal infections) range in degree from unnoticed to

fatal. They are directly related to asthma and allergic alveolitis

reactions. They are dealt with by the immune system and competition from

other microbes or earlier developmental phases of their own cyclogeny.

Fungal infections can be classified as;

Superficial -- those that effect hair, skin, nostrils, genitals, and oral

mucosa

Subcutaneous -- those which occur beneath the skin

Deep -- those which effect the internal organs, lungs, liver, bones, lymph,

brain, heart, and urinary tract

These infections often occur in those on long-term antibiotic therapies,

corticosteroids, and immunosuppressant drugs. This type of opportunistic

infection is common in those with the acquired immunodeficiency syndrome,

commonly known as AIDS, and also CFIDS (chronic fatigue syndrome).

Primitive bacterial varlents (thecits)

Some of these fungal forms are received from the environment, are

transmitted sexually, or are transmitted through mother's milk (Candida

albicans). Candida remains in non-virulent phases of development until the

terrain allows for its progression into more complex pathogenic forms. The

efficacy of many of the SANUM fungal remedies is based on the sexual

activity of the particular species of microorganisms (and/or the benign

effect altogether, through competition, on the terrain) which is initiated

through the process of reinstalling the microbial flora in the body in it's

apathogenic earlier phases of development. The flora that was installed then

copulates with the pathogenic variety and shares the sexual information of

the earlier phases, which, all things being equal (terrain modulation,

removal of stressors, proper diet, lifestyle, etc.) causes the pathogenic

form to convert or be reduced to the apathogenic variety. It is believed

that the pathogens are also reduced in valence through the actual activity

of the copulatory process.

The main causes of pathogenic albicans overgrowth are indiscriminate

antibiotic application and dental inclusions from mercury tooth amalgams.

Other factors include addictions to coffee, chocolate, drugs, unsafe sexual

practices, immuncompromisation, stress, chemicals, radiation, improper diet,

etc.

The fungal overgrowth occurs because its natural competitors have been

removed, in the case of antibiotic usage. In the case of dental amalgams or

metals, it is due to decreased immunity from immunocompromisation. The

candida also adsorbs the mercury in the gut, thereby serving the function of

keeping it from moving deeper in the system, to some degree. A good

inclusion in a program of remedies for alleviation of mercury toxicity in

the nervous system and brain is broken cell wall chlorella, because not only

is it similar to the fungus in that it adsorbs the mercury, but also carries

it away.

Primitive bacterial variants and cell wall deficient fungal species

I begin this section with a quote from " Cell Wall Deficient Forms: Stealth

Pathogens " by Lida Mattman.

" Wall-deficient bacteria are called fungoidal as they produce yeast-like

(emphasis added) budding spheres or simulate molds with elongated branching

threads. (See chondrothecit and free chondrit plates, respectively). How,

then, does one solve the dilemma of recognizing a wall-deficient fungus ?

One can start with the vital activity in a fungal filtrate of Candida

Albicans where the tiny 0.15-µm particles cannot possibly possess the wide

hard wall of the parent. Colonies developing are usually comprised of

twisted Gram-negative skeins so delicate that their course is interrupted by

submicroscopic gaps. These fine threads of growth have never been described

as part of the classic growth of fungi. (Emphasis added where bolded). "

The above description corroborates the findings of Dr. Günther Enderlein

when he described such coccoidal manifestations as being either primitive

bacterial variants or the most primitive mycelian strands.

Species of microorganisms which exhibit fungal variants in tissue (in vivo)

are only microscopically visible in the blood as the most elementary and

minute primitive spore forms, ranging in size up from approximately 0.15

microns. The notion that anyone is viewing fungus balls in phase contrast or

darkfield is technically a complete misconception, as the forms which are

being regarded as fungal developments are appearing in an alkaline milieu in

the blood which will not support the fungal stages of development. This is

not to say that the microorganisms may not be a species that can represent

fungal developments elsewhere in the body. But this species specificity is

indeterminable by viewing the fresh live blood, as there is not a way to

distinguish which species is being viewed without culturing it out through

the use of a medium, or by aging or heating the sample, under some

conditions. This process changes the phase of development into phases that

do not appear, again, in the alkaline milieu of the blood. The forms that

are being viewed (and mistaken for fungus stage) are actually colloid

thecits, thrombocytes, chondrits, ascits, synascits, and mychits, all of

which are part of the bacterial phase of development, which develops in an

alkaline milieu. Also, the cell wall deficient forms, chondrits which are

symplastic, are mistaken for fungal appearances. These chondrits do

represent a fermentative process, but not at the level of a fungal

appearance. They are even an earlier stage appearance than the most

primitive cell wall mediated bacterial variants. The species, again, are

unspecified upon appearance, as they are the same common stages that appear

in many species of microorganism developmental cycles.

Some of these developments in polymorphic progressions are actually

thrombocytes, and act as regulators, per Dr. Enderlein, and even (in some

species) emerge from the red corpuscles in the serum. Some of these ball or

balloon-like forms may become functionally pathogenic under certain specific

terrain related conditions, and conversely, some of these devlopments

certainly are an expression of the body's capacity to mount a defense. The

possibility of making these determinations within this phase of bacterial

cellular developments requires that the viewer be able to distinguish the

number of nulei which appear within these delicate diaphonous bacterial

cells. This microscopic imagery is only obtainable in a true, ultra

illumination darkfield, employing superior plan achro or plan apo medical

grade oil immersion iris diaphragm objectives and the proper condenser,

which would be of the oil immersion variety also. This determination of the

developmental progression of the bacterial variants is generally not able to

be made in a phase contrast or differential interference field

microscopically, because these fields generally do not provide adequate

resolution to count the nuclei which appear within the ball-like cells that

develop in conjunction with their primary nuclei (which are the cell wall

deficient symprotits until they develope this cell wall mediated

appearance). This is a crucial determination which must necessarily be made

in order to distinguish the function which is related to the cell's very

appearance.

It should also be noted that the pathogenicity of most microbes only exists

in one stage of development, being either viral sized, bacterial or fungal.

The exception to this is the Endobiont, Mucor racemosus Fresen, wherein any

stage above the primitive stages is pathogenic.

Candida is never observed in its fungal phase in the blood because the

blood's inherent alkalinity supports it's development only to a spore stage.

These spores are extremely minute, and do not progress to visibility at the

level where they can be distinguished from other similar microorganisms in

the blood except possible through staining. The primitive bacterial phase

microorganisms that are mistakenly called fungus may be part of the

developmental phase of a species that has a fungal variant or may culminate

as a fungus, but it is an error to call it a fungus in the blood. It is a

species that has a fungal variant, and may also have a bacterial phase that

occurs in the alkaline milieu of the blood. the ball-like appearances are

bacterial phase developments.

These so-called 'fungal balls' appear very similar to each other, regardless

of the number of nuclei, in phase contrast, but differ greatly in the higher

resolution of Ultra darkfield. In the Ultra-darkfield the number and valence

of the nuclei determines their status as potential regulators or pathogens,

and it is a mistake to classify them all as the same thing, or as having the

same function. Therefore, there may be a thecit (primitive bacterial) phase

in the life cycle of the species Candida Albicans. It follows that if

Candida appears in the blood, it may exhibit a bacterial phase rather than

the fungal phase, or certainly will appear as cell wall deficient spores.

Virus is a primitive stage of development of all microorganisms share and

this phase is virtually invisible in the present context of known light

microscopy techniques. Microbes are ubiquitous and can rise to their

pathogenic phase from any other phase, as their progression is not linear,

and the progression is terrain dependent. One must know which stage is

pathogenic in order to treat related conditions. For instance, acid-fast

rods are not necessary for tuberculosis.

Candida Albicans

This may be one of the most controversial and misunderstood areas in natural

health, especially as related to the correction of this fungal condition. I

have observed more individuals with failed programs for this condition than

any other. And by failed program, I am referring to ending up on what I call

the " coping diet " . Candida sufferers know this one well. It is the one where

you live on this very weird, limited diet and supplementation regimen

because you have been unable to determine and reverse the stressors that are

causing and maintaining the problem. This problem of epidemic proportions is

where great numbers of the victims of indiscriminate antibiotic use and

amalgam dental fillings recipients have ended up.

Pathogenic albicans (chronic candidiasis, more commonly known as candida or

thrush) is generally caused by drug use, particularly antibiotic drug use,

and poor diet, lowered immunity altogether, and metals, especially dental

amalgams. Mercury will promote the growth of Candida, as it adsorbs the

mercury and thereby protects the system. Candida cannot be effectively dealt

with without dealing with the dental issues first. This is not an optional

appraoch, but necessarily part of the primary approach.

The progressive decline which occurs as related to these mycotic conditions

does so in this order. First the antibiotics (which are aimed at E-coli,

strep, staph, etc, infections) wipe out the benign and necessary floras in

the gut. The presence of these benign floras (L. acidophilus lactobacillus,

bulgaris, B. longum, L.plantarium, L. salivarius, S. faecium, S.

thermopilus) is necessary for the equilibrium in the flora system which

keeps the competing (potentially pathogenic) yeast forms in check and allows

these ever present yeast forms to be a natural occurrence which is

apathogenic. The natural balance is maintained through competition of the

multiple microbes which are present. It is interesting to note that many

physicians treat this condition with additional antibiotics, causing

tremendous problems. Many use Nystatin or other antifungals which can cause

the creation of a resistant strain of fungus. They just mutate around it.

The preferable remedies would be benign pro-biotic remedies such as SANUM

Albicansan, Fortakehl and Pefrakehl which neither create nor further these

harmful situations.

When their natural regulators and antagonists are wiped out through

antibiotic drug use, the potentially harmless floras (colloids), which are

generally kept in check, become more highly developed and propagate in

massive numbers in the gut and tissues ( and thereby contribute to a

conversely high alkaline pH in the blood), while producing their own species

specific acids which maintain the terrain that they require for their

maintenance and propagation. In this environment they become more and more

virulent and even penetrate and root into the intestinal walls and invade

the cells. These fungal microorganisms become quite at home in the cell, and

can be considered to be a third primary potential parasite, along with Mucor

and Aspergillus, because of the advent of runaway antibiotic useage over the

many years. The only difference is that there is no known symbiosis occuring

from the presence of Candida Albicans in the body.

Certain vegetable species colloidal microorganisms produce particular acids

to maintain their environment. Examples of this are:

Mucor lactic acid

Aspergillus citric acid

Penicillin penicillic acid

The developmental life-cycle of microbes require differing pH conditions.

Some microorganism species find their culminant phase of development in the

bacterial phase. The different phases of development of microorganisms

require the following terrains for development:

virus, microbe, or primitive form strongly alkaline

bacterial phase weakly alkaline

fungal phase acidic

This developmental process is related to leaky gut syndrome, as the tissues

are weakened, even by the infection. The microorganisms continue to multiply

and then invaginate the venous wall (in spore form) and are carried again

out of the bloodstream and multiply in the tissues where they deposit their

acids, thereby enhancing the acid pH which they require for propagation.

This is why individuals with candida feel acidic. At this point in the total

progression of the problem, it is not just because their diet is acidifying.

An acidifying diet may be one of the original factors which contributed to

this complex problem, though. At this stage it probably will not be possible

to balance the pH through diet alone, because of the proliferation which is

creating and mainaining its own environment, at that point, through the

processes inherent to its upward development which are related to the

production of acids. To achieve the necessary optimum pH balances, these

individuals must use some combinations of Alkala (or other bicarbonate

combinations), baking soda baths, lemon juice and maple syrup combination

(juices only where tolerated), fresh pineapple juice, and electrolyte

solutions such as Cell Food, macro minerals, and all citrus fruits and their

juices (again, if tolerated). At this point the reader may think " Fruit

juices are full of yeast and sugars. Doesn't this feed the yeast? " . This is

true, but the point should not be to try to create a dietary approach in

order to cope forever with the problem, but rather to just create a diet

which is tolerable and supportive to elimination and then to deal with the

problem therapeutically with other meeans being the primary methods. The

imbalance is not created strictly by dietary imbalances and is not

eliminated in this fashion either. I will elaborate to some degree on these

approaches further on in the article.

pH balancing and gut flora enhancement or replacement alone will not affect

this condition, and most practitioners experience temporary results or

failure if they attempt this in combination with an exclusively dietary

approach. Most will find some relief with this approach (diet combined with

flora replacement) but will then end up living off of the shelves of health

food stores, on a continual supplementation regimen that addresses some

percentage of the associated symptomology and pathology. The reason for this

failure is that the candida has the upper hand in the gut and also

systemically, and has to be weeded out first or simultaneously, through

utilization of therapies that the yeast cannot mutate around (as in the case

of Nystatin and other antifungals).

These therapies may include SANUM remedies (isopathic combinations), ozone,

colloidal silver, Beck's box, and Rife type or other electromagnetic field

generators. These therapies may be effective in numerous different ways and

for varying reasons nad must be recommended and guided by an experieinced

practitioner who will know how to combine all of the different elements.

Often individuals expect immediate, symptomatic relief. In reality, one

should expect to feel worse first, as a great deal of eliminative activity

is in order. So it is important to understand that this condition was not

created in all of its severity overnight, and it may take a fair amount of

time in order to reestablish balance. For severe fungal infections a good

approach is to utilize Utilin, Latensin, Pefrakehl, Notakehl, and

Albicansan, w/ Alkala, colon cleansing, and kidney and liver drainage.

Again, the stressors must be removed first or simultaneously.

The SANUM remedies reintroduce the original form of the microbe which

appears in the body and is harmless, before it mutated. In a regualted pH

environment this benign form copulates (exchanges information) with the

pathogenic forms and they devolve into their original apathogenic forms and

can be maintained in thqt range of development.

The mode d' employ of Rife generators is to disturb the microbe's

progression through the application of electrical Herzian fields and also

through the stimulation of interleukin II and other immune factors.

The Beck box emits pulsed micro-amps causing the blood and tissue cell

membranes to oscillate, thereby interfering with the microorganisms ability

to parasitize the cell by entering it an using its componenets and

protection from the immune system. The cell membrane opens and closes

rapidly, flushing the serum in and out, taking with it microorganisms which

would otherwise be using the cell interior for its store of nutritional

reserves and as an environment in which to replicate or develop into more

advanced phases of manifestation. Simultaneously, nutrients are carried in

and out, and feed the cell at a much more effective level.

Ozone stimulates interleukin II, alkalinizes the body through the production

of ash, oxygenates the blood and tissues, and provides higher forms of

oxygen (03 through 013?, or higher depending how it is produced) which share

electrons with bacteria, virus, fungus, toxins, chemicals, and reduce all to

ash or nonpathogenic forms.

Colloidal silver interferes with the enzyme system that the anaerobic

microbes use for respiration. Therefore they cannot mutate around it or

become resistant and are eliminated instead. Special care must be taken with

colloidal silver to use one that is strong enough and simultaneously

supplement the gut flora, as the silver can also interfere with aerobic

microorganisms. Failing to supplement the flora, or using a product that

only contains 3 to 5 parts per million of silver, appears to be the main

limitations in terms of effectiveness. Naturally this approach, like any

other, must be accompanied by a full regimen that includes cycles of

purification, balancing, and rejuvenation. Contrary to popular gossip to the

contrary by invested promoters, there appears to be some negative side

effects to colloidal silver consumption, when used over long periods of time

and in relatively high amounts. These include drainage problems and the

destruction of intestinal floras. For some, the results of oral use have

been complicated gastro intestinal dysbioses and Fortakehl, Albicansan and

Pefrakehl and other SANUM preparations in combination may be a better

approach as they do not tend to produce those negative results.

Many individuals have been known to exhibit extreme Herxheimer's (healing

crisis) reactions with silver. This has particularly been a problem with

chronic fatigue syndrome. Lymphatic drainage (homeopathic, herbal, or 714-X,

which also regulates the immune system) along with juicing, consumption of a

minimum of eight 8 oz. glasses of Crystal Energy water and/or other natural

fluids such as juices and herbal teas, colonics or colemas, lymphatic

massage, dry brush massage, bouncing exercises, and walking are all required

in combination with colloidal silver and also the other aforementioned

approaches. It is not useful or necessary to load up the body with unnatural

numbers of metals such as silver over extended periods of time in order to

maintain good health. It is better to understand the overall biological

terrain requirements and meet them through the adjustment of lifestyle.

Nevertheless, it may be very useful to apply colloiddal silver for a

measured period of time because of its ability to interfere with the

repiratory enzymes of the microorganism. They also cannot mutate around this

effect.

Ozone will cause less of a negative reaction than silver. The reaction will

not as likely be a result of the breakdown of toxins, but rather congestion

in the lymph and liver. This is because the ozone reduces toxins to ash, so

they don't get recycled through your bloodstream as poisons on the way out

(and by association, through the brain). The Rife and Beck therapies also

require all of the same drainage requirements, and the lymphatic thumper

(Beck's design) may be useful while the fungus is being reduced The best

approach, as always, is to combine elements based on the individual's

tolerance and needs. Diet alone most likely will not correct this condition

of candida overgrowth, but is certainly a necessary adjunct to any program.

The dietary needs and reactions will be observed to change greatly after the

problem has been addressed.

Many people have been misled through the wrongly held beliefs of most

primarily dietarily oriented natural therapists on this subject. Therefore,

I recommend that practitioners understand that the microbe must be reduced

both in number and also to its apathogenic form, while ajusting the pH.

Acidophilus replacement is not the answer, as the higher phase dominant

yeast forms (which have overwhelmed the immune system's capacity to control

them) are at such a high valence that they just feast on or suppress the

installed lactobacillus strains when the subject is without proper

therapeutic intervention. This mycotic condition was not generally created

through dietary means alone, and although diet will be extremely necessary

and instrumental in a progrm of complete recovery, it will not on its own be

adequate therapeutically, which is the overwhelming and ongoing experience

of the numerous masses who are led in the direction of this belief. The

immune response is so overwhelmed that the body temporarily needs a " second

immune system " in the form of the aforementioned therapeutic approaches, or

other effective means.

All of the aforementioned therapeutic approaches (excepting Rife type

generators, for some) also relate to how to deal with Chronic Fatigue

Syndrome, although there are also many other factors, (especially

sociological) which need to be dealt with. See " The Four Underlying Causes

of Illness and What to Do About Them " by Coyle, for a more complete

explanation regarding these syndromes.

It may or may not be necessary for the client to eliminate all yeast

containing products (breads, cakes, pastries, yeast related supplements),

from the diet. The elimination of these foods is only necessary if they are

reactive to them. There is no sound basis to the notion that yeast, such as

brewers yeast, feeds fungus. Yet individuals with fungal conditions can be

reactive to almost anything, including yeast containing foods and food

supplements. Metals are also an extreme deterrent to recovery.

Since microorganisms compete for terrain in the body, it is a necessary and

useful corrective approach to supplement body floras once the proper

therapeutic inteervention has been established. The gut should contain a

great deal of beneficial microorganisms, even measurable in pounds. Flora

replacement is therapeutic in that the floras will compete with anaerobic

microorganisms and thereby reduce their number, especially once therapeutic

intervention has reduced the valence of the pathogens. This is why aerobic

gut microorganisms are considered to be an indispensable aspect of the

immune system, and should be present as at least 50%, and optimally 100%, of

the flora content in the gut.

An good formula for gut flora supplementation, both after and during a

program of correction of mycelium dysbiosis, is any flora product which

contains:

L. acidophilus

B. longum

L.planaterium

L. rueteri

L. salivarius

L. bulgaricus

E. faecium

S. thermopilus

Fructo Oligo Sacharrides

Calcium ascorbate

Trace minerals

Albicansan and Pefrakehl are specifics for fungus, and Notakehl and Okubasan

for reestablishing gut flora. The water drawn off of hulled barley, drunk,

is also useful in reestablishing flora. Use one part barley to one part

water, leave it overnight, and drink freely.

Many fungal disorders respond well to a series of courses of Latensin,

Notakehl, Pefrakehl, Fortakehl and Albicansan. Reactions may accompany these

remedies, and they should only be administered by a trained health

professional. These remedies are not antibiotic, but pro-biotic, and work

remarkably well. Because the type of fungal dysbiosis which is occurring

will not be determinable in the blood picture, the remedies must be applied

on the basis other forms of testing such as point testing, Kinesiology, etc.

A strong empirical understanding of how the condition presents and what the

primary stressors are in the subjects total life picture is likely the most

important means of evaluation of both condition and remedy.

About the Author

Coyle is a Natural Therapist, researcher and educator, and the

author of the definitive " NuLife Sciences Applied Microscopy for Nutritional

Evaluation and Correction " Workbook text. generally conducts monthly

or bimonthly training for health care practitioners in live-blood analysis.

For further information on NuLife Sciences and 's work and for a

schedule of training dates and a complementary microscopy equipment

catalogue, please see ad below. Also you may search under NuLife Sciences on

the worldwide web for further information.