PLEOMORPHIC MICROBES
PLEOMORPHIC MICROBES
The Hidden Cause of Cancer and Autoimmune Diseases
Walter Last
For nearly a century we had increasingly strong evidence for a common microbial cause of cancer and autoimmune diseases but now we also have visual proof. A newly developed research microscope can show us in great detail what happens in the blood of individuals who develop these diseases. What it shows is that the key for understanding their cause and cure is the rise, or perhaps better the uprising, of an endogenous microbe in the blood.
Based on the work of Louis Pasteur in the late 19th century the scientific community adopted the concept of monomorphism. This means that microbes always maintain their basic shape as virus, bacterium or fungus. The term pleomorphism, on the other hand, as coined by the French chemist and biologist Antoine Béchamp (1816–1908), refers to the ability of microbes to change from one form into another, similar to a caterpillar changing into a butterfly.
Historical Evidence
While a causal correlation between cancer and microbes has been shown only in a few rare or animal tumours, several independent researchers have reported the proliferation of certain microbes in all cancer patients. One of the first was the German professor of zoology and microbiology Günther Enderlein who described in 1925 the different stages of a microbe that is normally present as tiny colloidal protein units.
These protein units appear to originate from the natural breakdown of cellular components and may be essential for healthy blood. In degenerative diseases, especially cancer and autoimmune diseases, but also Chronic Fatigue Syndrome and Fibromyalgia, these protein units grow into increasingly higher bacterial forms and finally into fungi. In conventional terminology these forms are usually called Enderlein structures and are the basis of Live Blood Analysis as presently used in natural therapy.
Independently, mostly without knowing of each other's work, several other researchers - including Royal Raymond Rife, Wilhelm Reich, Virginia Livingston-Wheeler, Alan Cantwell and Gaston Naessens - have described the same phenomenon. Orthodoxy, however, has a dogma that says microbes always have the same form and cannot change from viruses into bacteria and fungi. This is because orthodox microbiologists commonly observe dead stained microbes in dead tissue, or live ones for short periods, instead of live microbes in live tissue at very high magnification over long periods.
Most pleomorphic microbes appear to be mycoplasma. They were discovered in 1898 and are the smallest group of bacteria. The term "myco" indicates fungus-like properties while "plasma" points to the soft shell without a cell-wall. They are actually living particles of bacterial nucleic acid and are regarded as being parasites in our body. Most mycoplasma are so small that like viruses they go through bacterial filters and may contaminate blood used for transfusions. Often mycoplasma infections remain symptomless until one suffers a traumatic event or when health deteriorates for some other reason. Because of the missing cell wall mycoplasma do not respond to most antibiotics ().
The microbe that causes Lyme disease from tick bites has been shown to exist in a bacterial as well as in a cell-wall deficient mycoplasma form. This is a main reason why it is so difficult to eradicate, and it has also been shown to be present in most of the tested chronic diseases, including Parkinson's disease, Alzheimer's disease, and autoimmune diseases. Parkinson's disease could be cured by eliminating the mycoplasma. Also other parasites are commonly present in Lyme disease. Researchers could grow 16 different bacterial types from one bacterial type simply by using different culture media. US government scientists hold a patent on behalf of the US Army of a crystalline form of mycoplasma which apparently can cause diseases such as AIDS, chronic fatigue syndrome, Wegener’s Granulomatosis, Sarcoidosis, lupus and Alzheimer’s Disease (.ec/sciencelib/4lyme/Townsendhowens.html).
Of special interest are experiments of Dr Livingston-Wheeler who injected cultures of pleomorphic organisms into mice. When small amounts were injected then an autoimmune disease tended to develop but higher doses produced tumours or cancer. Accordingly these cancer-forming microbes have often been called cancer viruses or cancer microbes.
The new Microscope
A new concept in optical microscopy is the grayfield method as developed by Kurt Olbrich (). This allows one to see detailed structures that are otherwise not even visible with conventional phase contrast microscopy. Now it is possible to observe the decomposition of live blood or the pleomorphic changes from spores or viral forms to bacteria and fungi in diseased blood.
Previous researchers of pleomorpic processes were restricted to a magnification of about 2000 times and a resolution of 200 nm while this method allows magnifications of up to 30,000 times and resolutions of less than 100 nm with great depth of focus in natural colours. Therefore everything can now be seen in much greater detail, and even be filmed. Orthodox microbiologists have used conventional analytical methods and theories to prove that the observed Enderlein structures are dead protein aggregates, but if they would instead use the Olbrich method and film the development and movement of these entities then they would be unable to defend their dogma.
I recommend that you watch these two videos: humoral_pathology.html runs for 22:34 minutes and shows the activity and development of pleomorphics in the blood. A longer video made earlier and of lesser quality but showing additional interesting scenes is at symbiosis_or_parasitism.html (50:50 minutes). Disregard the scientific details of the explanations, and especially the difficult-to-understand names of the various microbes and processes, and just focus on what you see. Even watch it all a second time to let it better sink in.
See files/sanguinogramm.pdf for detailed drawings and descriptions of the development cycle of these pleomorphic microbes. In the head of these club-shaped microbes one can see new spores or viruses evolving, and when the whole structure reaches a certain size the head explodes and releases a new batch of virus-size particles into the blood. Immune cells or phagocytes gobble up these virus forms, but if there are too many they just continue to develop inside the phagocytes into club-shaped forms. These eventually break out again with large heads full of viruses that they release into the blood.
The Nature of Pleomorphics
These videos show that healthy blood is clean with well-formed red blood cells, also called erythrocytes. In addition there is a faintly perceptible background structure of tiny globules with a single tail. During an acute infection some of these globules grow much bigger and develop a second tail, but after the infection has cleared up they disappear again. If the body is generally more unhealthy or in a so-called pre-cancerous condition then these structures remain permanently visible as round or elongated club-shaped forms.
An interesting phenomenon is the movement of these globules in and out of erythrocytes. Pleomorphics live mainly on our blood sugar, and when it is high they are mainly outside in the plasma but with low blood sugar they move back into the erythrocytes where they find more food. Then after eating sweet food they come back out again.
As the immune system continues to deteriorate fungus-like forms with long threads develop and grow increasingly bigger. The rigid and flexible fibers shown in the pleomorphic videos reminded me of the weird-looking specimens of Morgellons disease that I once viewed were strange fibers come out of the skin. Perhaps Morgellons is the result of semi-synthetic crystalline mycoplasma species developed by the US Army. The time-line shows that the first patent application was in 1986 and the final patent granted in 1993, while the term 'Morgellons disease' was coined in 2002. Successful self-help methods for Morgellons on the Internet seem to be effective against mycoplasma in general.
Large fungal forms are present at the end-stages of cancer and Aids. It is recognised that frequently the cause of death is due to systemic fungus infestations or mycoses. Conventional theory assumes that these are secondary to tumours or the AIDS virus, while the developmental cycle of the pleomorphics shows that these and their fungal stages are the primary cause why people die of cancer and probably AIDS. The reason for the lethal effects of severe mycoses is probably a combination of poisoning of the energy-producing mitochondria inside cells by fungal toxins and the destruction of erythrocytes by pleomorphic microbes.
These pleomorphics not only fill the inside of red blood cells and deplete them of nutrients, they also form spines and long protrusions in the cell wall when they move out into the plasma. Someone with myasthenia gravis, an autoimmune disease, once mentioned that he was shocked to see that most of his red blood cells looked like black sea-urchins. These erythrocytes can no longer supply nutrients to the body and are quickly destroyed in the spleen.
This is the real cause of severe anaemia that is so common in advanced cancer and various other diseases. In the end stages of cancer nearly 100% of erythrocytes are strongly infested and dysfunctional. This then leads to cachexia (muscle wasting with extreme fatigue) as the leading cause of death in cancer and AIDS. However, according to one of the videos and a related article in German, by using special vaccines developed by Enderlein even in an advanced stage of cancer the erythrocytes could be returned to a healthy condition within one month accompanied by the simultaneous shrinking of existing metastases.
You may wonder how it is possible for a single cause such as an overgrowth of the blood with pleomorphics to lead to many different diseases. The answer is basically the same as why a cyclone can destroy one building and leave another one undamaged, or rips off the roof of one and causes water damage in another. When the immune system is severely weakened then any pathogens present have free range to spread, and the weakest organ will be the first to crumble.
Orgone Experiments
These new observations with a superior microscope also validate the orgone experiments of Wilhelm Reich. He described similar microbial processes in the 1940's (The Cancer Biopathy. Ferrar, Straus and Giroux, NY, 1973). However, these experiments generated even more controversial results which were so threatening to the medical establishment that in 1956 and 1960 all of Reich's books were burned and equipment destroyed under FDA supervision and, because he maintained that a court was not a proper place to discuss a scientific theory, he died 1957 in an US jail (biography.html).
His most important discovery, which I regard as the greatest scientific achievement of the last century, was the bion as the basic unit of biological life. He found that every kind of food and vegetable matter when heated to incandescence and then dropped into a sterile nutrient solution evolved into round moving or pulsating forms that appeared blue in dark-field or when viewed with a fluorescent microscope. Reich sacrificed fine structure details and observed mainly at 3 - 5000x in order to better see colour and movements.
The stronger the blue colour, the higher the vitality of the entity. Under these conditions healthy erythrocytes have a strongly blue appearance while dead ones are black. According to Reich this blue glimmer is the characteristic of bio-energy or life-force which he called orgone. It is present not only in all living matter but also in water and air. Orgone originates in the sun and is transmitted by sunshine. Bions, the biological units of orgone, may gradually aggregate and evolve into amoeba-like or protozoan structures.
Reich described another formation which is derived from degenerating proteins as T-bacilli, which stands for the German 'Todes Bacilli' or 'death bacilli'. These can easily be cultivated from cancer tissue, the blood of patients with cancer or precancerous conditions, and also from degenerating blood. Injected in high doses they can kill mice within 24 hours, in lower doses they produce cancerous growths. They are black, lancet shaped and of similar size as described by Olbrich.
Also interesting is the observation that the blue bions paralysed and killed the black T-bacilli and even the much bigger proteus bacilli. In the same way strongly blue erythrocytes killed T-cells and pathogenic bacteria, but thereby the erythrocytes lost some of their blue colour, indicating that their vitality diminished in the process.
When strongly charged red blood cells entered a tumour, cancer tissue started to disintegrate into non-motile T-bodies. But in addition also the red blood cells disappeared and only T-bodies remained visible. The tumour developed large cavities which filled up with T-bodies. Macroscopically the originally blood-red cavities turned into a rust brown colour from the disintegrating tumour and blood cells.
Reich observed that weak erythrocytes could be charged to become strongly blue and vital by using sunshine and especially his orgone accumulator which concentrates orgone from the atmosphere. Some healers have the ability to channel strong bio-energy with their hands and to some degree even remotely with their mind.
Degenerating Blood
All cancers, autoimmune diseases and chronic infections seem to be associated with degenerating blood. This becomes apparent from the weak orgone charge of red blood cells and the presence of pleomorphic microbes in both plasma and erythrocytes. The weaker the blue colour and the more widespread and evolved the pleomorphics, the more is the blood degenerated and the more advanced is any chronic disease.
Also there is a concern that blood used for transfusions can be contaminated with mycoplasma. This, as well as the formation of T-bacilli in degenerating blood, may be factors in the observation that transfusions often lead to worse outcomes than giving no blood (article/817715.do).
Therefore it is important for us to understand the factors that cause blood to degenerate. A main cause is the presently widespread 'leaky gut syndrome'. In this condition the intestinal wall is permeable to microbial products present in the intestines, and also to only partly digested proteins which can now enter the blood. This greatly weakens not only the immune system, which tries to keep the blood clean, but also the vitality of red blood cells which become increasingly susceptible to invasion by pleomorphics.
Leaky gut syndrome appears to be a frequent outcome of antibiotic and chemo therapy and of various other drugs that interfere with our intestinal flora. This allows Candida and other pathogenic microbes to take over and invade the intestinal wall, causing inflammation and making it permeable. An associated factor is the presence of chronic infections and inflammations in other parts of the body.
Further implicated are any conditions that reduce our vitality, such as stress and worry, pharmaceutical and recreational drugs, processed food and nutritional deficiencies, exposure to microwaves and electromagnetic radiation, root canal treatment, fluoride and mercury as from amalgam fillings, and generally pollution of any kind.
According to Reich T-bacilli originate from the degeneration of every type of protein. This degeneration starts when proteins lose their vitality. There are two common forms of protein degeneration to which we are almost constantly exposed. One is the inappropriate use of cooked food, and the other is the gradually accumulating protein waste in our tissue.
Food can lose its vitality through cooking, storage or various mechanical processes. Food begins to lose vitality immediately after cooking, and a few hours later it has completely disappeared. Therefore, if we eat soon after cooking we still get much of the original vitality but the next day this cooked food may become a source of T-bacilli in the body. It is not clear how far this can be prevented by complete enzymatic breakdown during digestion but it is likely that some T bacilli will be able to enter the bloodstream. In a similar way does fresh food lose its vitality during long or inappropriate storage or mechanical processing, and can then become unhealthy. This should not be a problem with properly dried food and baked products.
Another observation of Reich may provide a solution. If bions are mixed with T-bacilli then the latter will be eliminated. Therefore if we mix some fresh food high in vitality with devitalised food then the overall body reaction will be positive. This also ties in with the observation that cooked food tends to cause digestive leukocytosis. This is an increase of the number of white blood cells after eating cooked food, indicating the presence of something toxic, but this reaction does not occur after eating raw food. Apparently leukocytosis can be prevented by adding some raw food to cooked food.
It would be good occasionally to check the vitality of your food. Traditionally this has been done by psychic means as with a pendulum but now also an objective instrument is available and even affordable. This is the Experimental Life-Energy Field Meter (cart/ylemeter.htm). It sells presently at $US 360 so that a group of individuals could easily share in its cost and use.
The second form of protein degeneration which is of major concern is the accumulation of protein wastes inside cells and tissue. This happens generally as we age, and is especially noticeable in all kinds of degenerative diseases. Up to 70% of the volume of some cells can be filled with stored decaying matter. This problem arises mainly from habitually eating proteins without their natural enzymes. Most of these enzymes are destroyed by heating over 45 degrees C. The solution is either to eat mainly raw food, or under-eat, or have periodic raw food cleanses.
Regenerating the Blood
It should now be obvious that the most important requirement to overcome a chronic disease, or to become really healthy and make our body disease-proof is the regeneration of our blood. We need to remove any highly developed pleomorphic microbes, and recharge our red blood cells with vital energy. This is the goal. When the blood has been regenerated then the immune system seems to be capable of eliminating pleomorphic invaders also in tumours and affected organs. This then tends to shrink tumours and stop so-called autoimmune attacks.
Our effort should start with sanitising the gastro-intestinal tract by using a combination of anti-microbial remedies and broad-spectrum probiotics. This should be continued for several months or until any related disease symptoms are under control. For a recommended program see ultimatecleanse.html. Combine this with a high-quality diet high in fresh raw food (e.g. HF2-1.html), preferably a moderate exercise program and suitable outdoors activity. Try to minimize the negative factors mentioned in the previous section.
A good way to check your progress is with Live Blood Analysis. If it does show problems in the blood then have another check about every three months until the appearance is normal. I generally recommend to follow your own program rather than mixing it with other remedies that may be offered. Another possibility is to use a Life-Energy Field Meter to monitor the vitality of your blood and urine.
Some special consideration may be appropriate for overcoming cancer, especially if a large tumour or metastases are present. There are several possible approaches.
You may focus mainly on restoring vitality. Wilhelm Reich did his with his orgone accumulator. While tumours tended to shrink or disappear, many of his patients died because of the toxic effect of disintegrating large tumours. His assessment was that they died because their organs of elimination were congested and could not cope with removing the released toxins.
The Gerson Diet is based on fresh vegetable juices to provide vitality and strongly focuses on eliminating the generated toxins. This gives it a much better success rate. I see the main disadvantage with this approach in that it tends to lead to massive periodic inflammations or healing crises as the immune system attacks the pleomorphics and any tumours. With juice-based diets one also needs to be careful not to unduly raise the blood sugar level when drinking juices of sweet vegetables, such as carrots. Therefore, at least half of such juices should be from green-leaf vegetables, and be sipped gradually.
Such inflammatory crises can be avoided by greatly restricting food intake as with the Grape Diet on about 1 kg of grapes spaced out during the day. Another example is the Breuss Diet on half a litre of fresh vegetable juice sipped during the day. Both diets are scheduled to last for 6 weeks. With this approach the body tends to auto-digest any tumours, and the pleomorphics seem to starve to death, but one needs to have reasonably good weight and energy to start with. Alternatively one may use several periodic raw-food cleanses of shorter duration.
Still another approach is to alkalise the body. Professor Enderlein found that pleomorphic structures dissolved in an alkaline milieu. We cannot make the blood itself much more alkaline then its natural slightly alkaline condition of about pH 7.4, but we can make the lymph system alkaline and with this any tumours. This may be done with different versions of sodium bicarbonate therapy, and in a more extreme degree with cesium chloride. This tends to eliminate tumours without much inflammation and also helps to clean the blood.
A variety of antimicrobial remedies and devices have been used for which there is widespread anecdotal and often also research evidence of efficacy. Most of these have also strong antifungal properties and often seem to work without generating strong inflammations. It appears that they mainly clean the blood. Without the presence of pleomorphics tumours just seem to fade away.
Some well-known examples are olive leaf extract, pau d'arco, kerosene, and Lugol's iodine solution; ozone and hydrogen peroxide if used intravenously; electronic zapper, and various electronic devices which radiate specific frequencies to destroy pleomorphics. Jim Humble () claims success with MMS (acidified sodium chlorite) but this is difficult to evaluate because of severe harassment and suppression by the FDA. Minocycline is a conventional antibiotic which has been successful with rheumatoid autoimmune diseases when used in very low doses over long periods. Therefore I assume that it also works by cleaning the blood and tissue of pleomorphics.
My own preference is to use a combination of high-quality diet with periodic raw-food cleanses, alkalising the body, and using moderate amounts of periodically changing antimicrobial remedies and devices. I also like vitalising the blood by exposing the veins under the arms and inside of the legs to sunshine. Continue these efforts until the blood appears to be clean and/or tumours have disappeared or are apparently dormant. For details see OvercomingCancer.html. The same approach is also suitable for autoimmune diseases and other degenerative conditions.
Conventional Medicine cannot adequately explain how tumours kill patients. The available evidence leads me to conclude that tumours are more or less harmless, and that it is mainly the blood contamination with pleomorphic microbes which is the real killer in cancer, AIDS and various other diseases.
© Walter Last 2011
................
................
In order to avoid copyright disputes, this page is only a partial summary.
To fulfill the demand for quickly locating and searching documents.
It is intelligent file search solution for home and business.
Related download
- endo—adrenal and parathyroid disease josh corwin
- pleomorphic microbes
- academy for fcps md ms pmdc step academy
- ncc pediatrics residency at walter reed bethesda
- diabetic ketoacidosis
- adrenal insufficiency acute developinganaesthesia
- science for the winegar ap biology
- elizabeth leen home
- learn the applications and benefits of iv nutrient