The new Microscope
A new concept in optical microscopy is the grayfield method as developed by Kurt Olbrich (www.grayfieldoptical.com). 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: www.grayfieldoptical.com/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 facts is at www.grayfieldoptical.com/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.
Also see www.grayfieldoptical.com/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-sized 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. In this disease strange synthetic-looking fibers come out of the skin. This suggests to me that Morgellons may be the result of the 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. It appears that the US Army started experimenting with mycoplasma soon after the end of WW2 as suggested by several strange epidemics such as the Royal Free Epidemic of 1955 involving Myalgic Encephalitis, now more commonly called Chronic Fatigue Syndrome or Fibromyalgia.
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 observed pleomorphic life cycle 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 pleomorphics.
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, as shown in the longer video, with special Enderlein vaccines even in advanced cancer the erythrocytes could be returned to health within one month with 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 or hurricane 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 have free range, and the weakest organ will be the first to crumble.
