Fulvic acid, a rather complicated organic acid
Obviously, there is a reason why chemists normally call this fulvic acid and don't even try to come up with the systematic name for it...
6.30.2007
Fulvic Acid
To see if you have mastered the principles of organic chemistry nomenclature, try determining the systematic name of what we normally call fulvic acid:
Fulvic acid, a rather complicated organic acid
Obviously, there is a reason why chemists normally call this fulvic acid and don't even try to come up with the systematic name for it...
Fulvic acid, a rather complicated organic acid
Obviously, there is a reason why chemists normally call this fulvic acid and don't even try to come up with the systematic name for it...
Somatoscope: Gaston Naessens
A revolutionary video showing the incredible microscope of Gaston Naessens, called the 'somatoscope' which breaks the laws of physics to show you living organisms at 30,000X magnification and 150 Angstrom resolution..... showing living organisms without any type of slide preparation or staining. You will see the Somatid which lives in all living organisms (including humans), which is a shape changing (pleomorphic) organism responsible for cancer and many other degenerative diseases. Naessens invented his incredible microscope over 40 years ago and has invented a substance called 714X which has successfully treated cancer and other degenerative diseases in many people
Gaston Naessens
is responsible for several remarkable developments which may revolutionise our understanding of life and bring a major advance in cancer therapy. His work started with the invention of an amazing microscope, the "somatoscope". This led him to the discovery of the Somatid Cycle, and in turn to the development of his serum, 714-X.
The Somatoscope
Naessens' revolutionary microscope, the somatoscope, weaves two light sources (one visible, one ultraviolet) together to produce a third, functionally higher, frequency with which it is possible to obtain a resolution and magnification thirty times greater then with conventional light microscopy . (In conventional light microscopy resolution, and therefore magnification, is limited by the wavelength of visible light - approximately 4000 Angstroms.) Although with the electron microscope there is almost no limit to the magnification, the electrons must be beamed through a vacuum, so it can not be used to look at living material. Naessens' remarkable somatoscope, however, can view live material with a resolution of 150 Angstroms, a magnification of 30,000 diameters. That magnification reveals a whole new world in a tiny drop of blood. The world that Gaston Naessens sees in that drop with his somatoscope is quite different from what we were taught at school! He sees that our blood is alive with a teaming micro-ecology. This is how Gaston Naessens discovered the somatid.
Somatids
In all living plants and animals Naessens observed tiny creatures. He called them somatids - "little bodies". He says that in the healthy organism the somatids have a simple three stage life cycle (a simple viroid form, spores, and double spores). This he named the microcycle. The somatids are symbiotic - they've always been with us, and we need them. However, when the body is under stress the somatids elaborate into a more complicated macrocycle, a sixteen stage cycle. The macrocycle is parasitic and is associated with the development of immune compromised diseases - such as cancer. Naessens' theory is that there are inhibitors in the blood that keep the somatids in the healthy symbiotic microcycle. Under stress these inhibitors may be lost and our friends, the somatids, turn into opportunistic parasites. So, in the 16 stage macrocycle bacteria-like and fungus-like forms grow from the somatids. This elaboration of forms is termed pleomorphism. The somatid pattern can function as an indicator of serious disease. The somatid pattern associated with cancer, for instance, is usually observed in the blood up to two years before the manifestation of the disease. This allows us to get a really early warning when we are headed for trouble or it can be helpful in keeping track of the progress of a preexisting disease. By monitoring the somatid phenomenon we can observe a patient's response to both orthodox and alternative treatments, and to life style changes.
Pleomorphism and Darkfield Microscopy
Although developed in isolation, Gaston Naessens' theories are part of a larger body of work that we may call "the darkfield work". His somatoscope is a very special variation of the darkfield microscope. All those who have worked extensively with darkfield microscopy, with live blood, have come up with similar stories of pleomorphism. In conventional "brightfield" microscopy we send light directly through the specimen, and so we can't see the specimen (thin slices of tissue, including blood, are transparent) unless we stain it. And to stain it we have to kill it. So again, as with the electron microscope, orthodox science, with all its sophistication, looks at dead material. With darkfield microscopy light is shone onto the specimen from the side. We look at reflected light against a dark background. This gives us a highly contrasted image. We don't need to stain the specimen, and therefore we can examine at living material. The darkfield microscope allows us to observe the somatid's pleomorphic cycles.
One of the first scientists who talked about pleomorphism in human blood was Béchamel, a contemporary and rival of Pasteur. He called the little bodies he observed "microzymes". Enderlein in the first half of this century called them "protits". In the 1930s Rife built a darkfield microscope comparable to Gaston Naessens'. He too saw pleomorphism.
Pleomorphism is a natural adaptive response of microorganisms. When the environment allows they are virus-like, bacteria-like, or fungus-like: they metamorphose to suit their conditions. When we are healthy they help us. According to Naessens they produce a growth hormone that is essential for cell division in all plants and animals. Biologist call this sort of mutually depended relationship "symbiosis". However, when we are unhealthy our friends, the somatids, turn on us and become parasitic. But this parasitism is a process that can be recognised by darkfield microscopy and it can often be reversed. Most important, we must find out what stressors caused the problem, and correct the situation.
714-X
Gaston Naessens' next invention was the development of a treatment that he calls 714-X. 714-X is a nitrogenized camphor derivative (trimethylbicyclo-nitraminoheptane). As I understand it the rationale behind this treatment is as follows: Gaston Naessens learned that tumours are nitrogen traps. They steal nitrogen from the body and this inhibits the immune system. By supplying nitrogen to the tumour and the body, the immune system is disinhibited, and the body begins to heal itself. (Camphor has a natural affinity for tumours and, as it is not toxic at pharmacological doses, it proved to be the perfect vehicle to carry the nitrogen to the tumour and the body.) The serum is injected "paranodularly" - that means next to the lymph nodes - so it is absorbed into the lymphatic system where it can act most directly. People close to Gaston Naessens' work believe that 714-X is best used early. While they believe it may save one in twelve of the terminally ill patients who turn to it on their death beds, and maybe one in six of the advanced cancer patients who try it as a last hope, when it is given early in the disease process, they feel that it might help almost everyone. Further, anecdotally, even in advanced cancer, 714-X may greatly improve quality of life.
The normalization of immune function is not only of benefit with cancer; 714-X is also thought to help to stabilize, though not to cure, AIDS, and to be of benefit with other disorders in which the immune system is compromised. To date no adverse reactions or side effects have been observed beyond some irritation at the site of injection.
In 1990 714-X was made available through Health and Welfare Canada's Emergency Drug Release Program and it can now be ordered by any MD. More than 800 patients have received 714-X, and it has recently been transferred from experimental to investigational status.
Gaston Naessens' remarkable work promises a whole new understanding of biology. It leads to a new perspective and, hopefully, a great advance in cancer treatment.
To make his work more widely accessible Gaston Naessens has designed a modified version of the darkfield condenser that allows the observation of the somatid cycle that he discover with his somatoscope. Under the banner of "The Canadian Institute of Alternative Medicine" I purchased Naessens darkfield system and offer the "somatid observation" in Toronto. Phone 416 928 9272 or email normanallan
Darkfield microscopy brings us a window into the body and a road to a new understanding.
Norman Allan, Ph.D., is a research scientist and practitioner of alternative therapies based in Toronto. For more information phone 416 928 9272.
Gaston Naessens
is responsible for several remarkable developments which may revolutionise our understanding of life and bring a major advance in cancer therapy. His work started with the invention of an amazing microscope, the "somatoscope". This led him to the discovery of the Somatid Cycle, and in turn to the development of his serum, 714-X.
The Somatoscope
Naessens' revolutionary microscope, the somatoscope, weaves two light sources (one visible, one ultraviolet) together to produce a third, functionally higher, frequency with which it is possible to obtain a resolution and magnification thirty times greater then with conventional light microscopy . (In conventional light microscopy resolution, and therefore magnification, is limited by the wavelength of visible light - approximately 4000 Angstroms.) Although with the electron microscope there is almost no limit to the magnification, the electrons must be beamed through a vacuum, so it can not be used to look at living material. Naessens' remarkable somatoscope, however, can view live material with a resolution of 150 Angstroms, a magnification of 30,000 diameters. That magnification reveals a whole new world in a tiny drop of blood. The world that Gaston Naessens sees in that drop with his somatoscope is quite different from what we were taught at school! He sees that our blood is alive with a teaming micro-ecology. This is how Gaston Naessens discovered the somatid.
Somatids
In all living plants and animals Naessens observed tiny creatures. He called them somatids - "little bodies". He says that in the healthy organism the somatids have a simple three stage life cycle (a simple viroid form, spores, and double spores). This he named the microcycle. The somatids are symbiotic - they've always been with us, and we need them. However, when the body is under stress the somatids elaborate into a more complicated macrocycle, a sixteen stage cycle. The macrocycle is parasitic and is associated with the development of immune compromised diseases - such as cancer. Naessens' theory is that there are inhibitors in the blood that keep the somatids in the healthy symbiotic microcycle. Under stress these inhibitors may be lost and our friends, the somatids, turn into opportunistic parasites. So, in the 16 stage macrocycle bacteria-like and fungus-like forms grow from the somatids. This elaboration of forms is termed pleomorphism. The somatid pattern can function as an indicator of serious disease. The somatid pattern associated with cancer, for instance, is usually observed in the blood up to two years before the manifestation of the disease. This allows us to get a really early warning when we are headed for trouble or it can be helpful in keeping track of the progress of a preexisting disease. By monitoring the somatid phenomenon we can observe a patient's response to both orthodox and alternative treatments, and to life style changes.
Pleomorphism and Darkfield Microscopy
Although developed in isolation, Gaston Naessens' theories are part of a larger body of work that we may call "the darkfield work". His somatoscope is a very special variation of the darkfield microscope. All those who have worked extensively with darkfield microscopy, with live blood, have come up with similar stories of pleomorphism. In conventional "brightfield" microscopy we send light directly through the specimen, and so we can't see the specimen (thin slices of tissue, including blood, are transparent) unless we stain it. And to stain it we have to kill it. So again, as with the electron microscope, orthodox science, with all its sophistication, looks at dead material. With darkfield microscopy light is shone onto the specimen from the side. We look at reflected light against a dark background. This gives us a highly contrasted image. We don't need to stain the specimen, and therefore we can examine at living material. The darkfield microscope allows us to observe the somatid's pleomorphic cycles.
One of the first scientists who talked about pleomorphism in human blood was Béchamel, a contemporary and rival of Pasteur. He called the little bodies he observed "microzymes". Enderlein in the first half of this century called them "protits". In the 1930s Rife built a darkfield microscope comparable to Gaston Naessens'. He too saw pleomorphism.
Pleomorphism is a natural adaptive response of microorganisms. When the environment allows they are virus-like, bacteria-like, or fungus-like: they metamorphose to suit their conditions. When we are healthy they help us. According to Naessens they produce a growth hormone that is essential for cell division in all plants and animals. Biologist call this sort of mutually depended relationship "symbiosis". However, when we are unhealthy our friends, the somatids, turn on us and become parasitic. But this parasitism is a process that can be recognised by darkfield microscopy and it can often be reversed. Most important, we must find out what stressors caused the problem, and correct the situation.
714-X
Gaston Naessens' next invention was the development of a treatment that he calls 714-X. 714-X is a nitrogenized camphor derivative (trimethylbicyclo-nitraminoheptane). As I understand it the rationale behind this treatment is as follows: Gaston Naessens learned that tumours are nitrogen traps. They steal nitrogen from the body and this inhibits the immune system. By supplying nitrogen to the tumour and the body, the immune system is disinhibited, and the body begins to heal itself. (Camphor has a natural affinity for tumours and, as it is not toxic at pharmacological doses, it proved to be the perfect vehicle to carry the nitrogen to the tumour and the body.) The serum is injected "paranodularly" - that means next to the lymph nodes - so it is absorbed into the lymphatic system where it can act most directly. People close to Gaston Naessens' work believe that 714-X is best used early. While they believe it may save one in twelve of the terminally ill patients who turn to it on their death beds, and maybe one in six of the advanced cancer patients who try it as a last hope, when it is given early in the disease process, they feel that it might help almost everyone. Further, anecdotally, even in advanced cancer, 714-X may greatly improve quality of life.
The normalization of immune function is not only of benefit with cancer; 714-X is also thought to help to stabilize, though not to cure, AIDS, and to be of benefit with other disorders in which the immune system is compromised. To date no adverse reactions or side effects have been observed beyond some irritation at the site of injection.
In 1990 714-X was made available through Health and Welfare Canada's Emergency Drug Release Program and it can now be ordered by any MD. More than 800 patients have received 714-X, and it has recently been transferred from experimental to investigational status.
Gaston Naessens' remarkable work promises a whole new understanding of biology. It leads to a new perspective and, hopefully, a great advance in cancer treatment.
To make his work more widely accessible Gaston Naessens has designed a modified version of the darkfield condenser that allows the observation of the somatid cycle that he discover with his somatoscope. Under the banner of "The Canadian Institute of Alternative Medicine" I purchased Naessens darkfield system and offer the "somatid observation" in Toronto. Phone 416 928 9272 or email normanallan
Darkfield microscopy brings us a window into the body and a road to a new understanding.
Norman Allan, Ph.D., is a research scientist and practitioner of alternative therapies based in Toronto. For more information phone 416 928 9272.
6.28.2007
EM1 Effective Micro-Organisms
Developed by Dr. Teruo Higa of Okinawa, EM1 is a powerful microbial technology that is being used to solve many of our environmental problems today
This video was developed for the World Water Forum held in Kyoto in 2003. It shows uses of Effective Microorganisms Technology™ around the world for farming, water, wastewater, and composting.
How to Make Bokashi
This video was developed for the World Water Forum held in Kyoto in 2003. It shows uses of Effective Microorganisms Technology™ around the world for farming, water, wastewater, and composting.
How to Make Bokashi
6.23.2007
Belousov-Zhabotinsky-Reaction
"In 1951 the Russian scientist Boris P. Belousov discovered that if citric acid, acidified bromate and a ceric salt were mixed together the resulting solution oscillated periodically between yellow and clear. He had discovered a chemical oscillator. The scientific community was united in believing this to be impossible. Some years later another Russian biophysicist, Anatol M. Zhabotinsky ... refined the reaction, replacing citric acid with malonic acid and discovering that when a thin, homogenous layer of the solution is left undisturbed, fascinating geometric patterns such as concentric circles and Archemedian spirals propagate across the medium. Therefore, the reaction oscillates both in space and time, a so-called spatio-temporal oscillator.
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Aetheric Polymeric Matrix Material: Orgonite
