The world is quietly being led to the slaughterhouse. Very few give a damn. Especially the corporate media. Time to exterminate the ELITE!
Monday, November 16, 2009
Tuesday, November 3, 2009
Monday, November 2, 2009
Wednesday, October 28, 2009
The Swine Flu (aka 'H1N1) That's Not A Flu At All
Lawrence Broxmeyer, MD
The current Swine "flu" pandemic began in La Gloria, a pig-farming village in the Veracruz mountains of Mexico. Surely, if any place could unlock the true nature of the cause of the 2009 Pandemic, it would be found in La Gloria, whose villagers were certain that they were sickened by the surrounding pig farms, which they accused of polluting their air and water with pig waste. This is much like what happened in Haskell County, Kansas in 1918, original site of the Great Influenza Pandemic of 1918.
But Enrique Sanchez, top official from Mexico's Agriculture Department, could not find H1N1 in mucous samples taken from the pigs several weeks later, on April 30th. Common bacteria were also tested for. However no studies were done to rule out Swine tuberculosis which is predominantly avian and to a lesser extent bovine, and could have also accounted for the wholesale "respiratory" problems the villagers were experiencing.
Mexican health officials, overlooking the La Gloria situation initially, downplayed it, much as health officials everywhere are prone to do. Yet of 43 villagers whose mucous samples were taken, only one, a 5-year-old boy, was confirmed as having Swine Flu. So head investigator from the Biotechnology Institute of the National Autonomous University of Mexico there, Dr. Carlos Arias, told the AP:
"I cannot understand it. I could almost bet that there were more infections related to the virus."
Soon, more than half of La Gloria's 3,000 residents fell ill with FLU-LIKE illness, etiology unknown. 450 of the sickest of these where treated not with anti-virals such as Tamiflu, but with antibiotics and masks. What was the diagnosis handed out? Why it was "acute respiratory infections", and by the time the mucous results came through in early April, most of the villagers had recovered, the more serious cases on antibiotics alone. The "virus" seemed to have left their systems. But the question lingers: since antibiotics don't cure "viruses" what infectious disease in these purported "Influenza" victims had been cured by the antibiotics given?
On June 3rd, 2009 in Global Research, a curious article by F. William Engdahl appeared, entitled "Sarkozy's Secret Plan for Mandatory Swine Flu Vaccination". In it Engdahl plainly stated that "The only problem with the Swine Flu (H1N1) Vaccine, is that to date, neither WHO nor the US Government's Center for Diseases Control (CDC) have succeeded to isolate, photograph with an electron microscope, or chemically classify the H1N1 Influenza A virus". Furthermore there was no scientifically published evidence that French virologists have done so either. Therefore, mentioned Engdahl, "To mandate a vaccination for a putative (supposed or assumed to exist) disease that has never been characterized, is dubious to say the least."
Engdahl had done his homework. When questioned regarding the electron pictograph of H1N1 that the CDC recently came up with on their website, he revealed his source, German virologist Dr Stefan Lanka, an expert on the documentation of viruses, attesting to the fact that the H1N1 picture was bogus. The virologist wrote that he had "written the CDC many times as to who made the H1N1 photo's and whether they where scientifically documented as to chemical characteristics and other properties." There was never any reply. He concluded "If CDC refuses to cite the source of the photos, they are fake." Worse yet he said "The photos are merely liposomes, microscopic artificial sacs whose walls are a double layer of phospholipids, used to carry substances such as drugs, vaccines, and enzymes to specific cells or organs of the body. These have been artificially presented by a process where chick embryos or cell cultures are killed, reduced and then centrifuged with some solvent, to then, in a vacuum, be nanofiltered." As if this wasn't enough, the virologist testified that "Such a structure has never been characterized in either an organism or its fluids. Furthermore, if there wasn't for the centrifuge/solvent/nanofiltration manipulation, not to mention the precipitation procedure, such particles could never be presented under the electron microscope. In conclusion, without the isolation of the H1N1, there is no H1N1 infecting virus"
Engdahl wasn't finished. "Even more bizarre is the admission by the US Government's Food and Drug Administration, an agency responsible for the health and safety of its citizens, that the 'test' approved for premature release to test for H1N1 is not even a proven test. More to the point", continues F. William Engdahl, "there is no forensic evidence in any of the deaths reported to date that has been presented that proves scientifically that any single death being attributed to H1N1 Swine Flu virus was indeed caused by such a virus."
These thoughts were only strengthened when Engdahl looked into "Novavax, a US pharmaceutical company based in Rockville, Maryland, (who) conveniently enough just announced it is developing a vaccine for H1N1 based on 'virus-like particles'".
'Virus-like particles' do not mean virus. Viral-like, cell-wall-deficient forms of tuberculosis, for example, also appear virus-like and apparently.. so also did non-infectious liposomes.
Both the World Health Organization (WHO) and the Centers for Disease Control (CDC) are fully aware of a far more serious and ongoing tuberculosis Pandemic in the world today. Yet they choose to downplay the link, disregarding the similar flu-like symptoms tuberculosis often begins with.
WHO freely admits that there were approximately 1.8 million deaths from tuberculosis in 2007, the most recent year for which data are available as well as that presently about one-third of the world's population, or two billion people, carry the TB bacteria.
The "H" and "N" of influenza sub-typing, revolves around two glycoproteins called Hemagglutin (H) and Neuraminidase (N), both of which can be, and are, associated with infectious diseases such as the minuscule, viral forms of tuberculosis, a disease which ought to be high on the differential diagnosis for 'flu-like illness' . An August, 2008 Medline study in the Journal of Clinical Biochemistry showed that sputum neuraminidase levels over 1.0 mU per mL were proven associated with having tuberculosis in 92% of cases. Previous to this, bacteria closely related to TB were shown, through crystallization, to produce the same protein neuraminidase used to subtype 'Influenza'. Furthermore, as of 2006, it has become obvious in Menozzi's study that similar to Influenza, Tuberculosis not only uses Hemagglutin to attach to the lung's epithelial cells it invades, but requires Hemagglutin for dissemination of the disease to the rest of the body.
Khomenko's 1993 study, showed that the explosive contagiousness of just such influenza-like forms of tuberculosis are exactly the stuff that previous epidemics and pandemics could have been made of. Khomenko was mentioned by Nobel nominee Lida Mattman in her textbook. That is exactly why, that in response to the present world "flu" pandemic, Japan's Health Ministry's Tuberculosis Infection Diseases Control Division deputy director Takeshi Enami went hand in hand with Yoshio Nanba, director of The Office of Pandemic Influenza Preparedness and Response, to attend a news conference in Tokyo on May 1, 2009.
But back in the US, the CDC and NIH seem to feel differently, ignoring everything but "the virus". There was much the same "Influenza" talk when in 1990, a new multi-drug-resistant (MDR) tuberculosis outbreak took place in a large Miami municipal hospital. Soon thereafter, similar outbreaks in three New York City hospitals left many sufferers dying within weeks. By 1992, approximately two years later, drug-resistant tuberculosis had spread to deadly mini-epidemics in seventeen US states, and was reported, not by the American, but the international media, as out of control. Viral forms of swine, avian and human TB can be transmitted from one species to another. By 1993 the World Health Organization (WHO), proclaimed tuberculosis a global health emergency. (1)
1918 AND TODAY
No one can deny the similarities between the onset of the 1918 epidemic and that of today, yet a Press Release, issued on August 19, 2008, by the National Institute of Allergy and Infectious Diseases (NIAID), contains a striking finding and conclusion: The 20 to 40 million deaths worldwide from the great 1918 Influenza ("Flu") Pandemic were NOT due to "flu" or a virus, but to pneumonia caused by massive bacterial infection."(2)
Subsequently, a study published in JAMA by Talbot and Moore (3) in 2000 showed that Mexican immigrants to the US have the highest case rates for tuberculosis among foreign born persons. Mexico is the country where Swine Flu deaths were first documented.
The research of Lawrence Broxmeyer MD (4) first proclaimed that the 1918 pandemic was due to bacteria, particularly mutant forms of flu-like fowl, swine, bovine, and human tuberculosis (TB) bacteria:
( http://drbroxmeyer.netfirms.com/001pdfBIRDFLUEDITORIALPUBLISHED.pdf ).
These forms of tuberculosis are often viral-like, mutate frequently and can "skip" from one species to another. Moreover the antibodies from such viral TB forms react in the compliment fixation and later "viral" assays (5). They also grow on cultures which are supposed to grow only viruses.
In a supportive 16-page-paper which appeared in Population and Development Review, University of California demographers Andrew Noymer and Michael Garenne came up with convincing statistics showing that undetected tuberculosis may have been the real killer in the 1918 flu epidemic (6).
THE ROOTS OF HISTORY
Noymer's TB hypothesis stands sound against history. Few flu "experts" are aware that in medical texts printed circa 1918 "Influenza" was attributed not to a virus but a bacteria called Mycobacterium influenzae, discovered by Pfeiffer and Canon (7) in 1892......not exactly a coincidence since Richard Pfeiffer worked, at one time, for Robert Koch, the discoverer of tuberculosis, a disease also caused by another bacillus called Mycobacterium tuberculosis. Both mycobacteria stained best with carbol-fuchsin, a bacterial stain commonly used in the staining of mycobacteria as it has an affinity for the mycolic acids found in their cell walls. Mycobacteria such as tuberculosis are particularly deadly because they share properties of the fungi ("myco-") as well as bacteria. TB was, not all that long ago, referred to as "captain of the men of death". And it never lost its potential to kill.
Mycobacterium influenzae was considered by most to be the cause of influenza until 1933. But there were serious diagnostic problems with Mycobacterium influenza. Stengel and Fox warned (8) about them in their widely quoted W.B. Saunder's 1915 version of "A Textbook of Pathology". Problems with identification revolved mainly in that although the bacterial influenza occurred abundantly in the sputum of flu patients at first, it decreased in quantity as the cases advanced. And when purulent expectoration stopped, whether the disease was still active or not, Mycobacterium influenzae "disappears entirely"(8).
In 1933 English physicians Wilson Smith, Christopher H. Andrewes, and Patrick P. Laidlaw(9) removed secretions from the throat of a humans with flu-like symptoms thought to have "influenza", and then filtered out a suspected infectious agent, which by virtue of the fact that it went through a filter was falsely proclaimed, from the onset, to be "a virus". Injecting it into ferrets, the ferrets then developed the same flu-like symptoms which Smith, Andrews and Laidlaw summarily declared as "influenza". In addition Sir Christopher Andrewes suggested, with the help of Burnet and Bang, that the term "myxovirus", meaning "mucous virus", be incorporated into a family name for the Influenzas. This, one imagines, was because the organism came from mucous secretions.
But to government pathologist and pioneer physician/researcher William M. Crofton, who by virtue of his office as County pathologist had examined some of Laidlaw's human "Flu" samples, Laidlaw's entire study was flawed. Crofton found Laidlaw's Flu samples to be laced with the bacillus Mycobacteria influenzae, which by then had been renamed Haemophilus Influenzae. To Crofton this bacilli was the common denominator for the Pandemic of 1918 he had witnessed, although the bacteria could be accompanied by an array of opportunistic organisms such as Staph and Strep. Crofton publically and personally confronted and challenged Laidlaw to come to his laboratory for the proof that his Influenza samples weren't viral. Crofton was convinced by the confirmation of scientists like Calmette at Pasteur regarding how certain forms of tuberculosis, appearing both minuscule and viral, could pass through the smallest of filters. Crofton himself then established that tuberculosis could disappear into tissues as viruses did, and then go through filters which stopped cold even most of those "now invariably called viral disease". "Surely, then", Crofton concluded, "Tuberculosis has more right to be considered a true virus than these(10)." So, at a time when viral forms of TB where scantily being documented, Crofton struggled to link H. Flu with the TB it so often infected in coordination with, as historical and political momentum carried Laidlaw's study through for posterity. A great opportunity was missed to correct the record.
Frank Macfarlane Burnet was the first to grow "Influenza" in a laboratory setting; in 1940 he grew influenza in embryonated chicken eggs, using the allantoic sac. He obviously considered such a technique "Influenza" specific, never bothering to consider that such an allantoic site might also be an excellent site for culturing the viral or Cell-Wall-Deficient (CWD) forms of tuberculosis and the mycobacteria. Viral TB, in fact grows there as early as 6 hours after introduction into such a place in chicken embryos(11).
Furthermore, some of the filamentous forms of tuberculosis mentioned by Corper (12) appear similar to those attributed to ''Influenza'' by biochemist and Influenza guru Burnet (13).
It wasn't because Burnet didn't know that bacteria could assume viral forms. The first, and for a time the only virologist in Australia, it was Burnet who discovered bacteria in viral forms of Q-fever (14). And in that same paper, proclaiming Virology as an Independent Science , and after admitting that viruses, including influenza, are composed of the same sorts of material as bacteria, Burnet struggles to differentiate Influenza by the fact that it ''probably has no DNA'' and was therefore exclusively RNA.(Ibid.). But, according to Xalabardar, some cell-wall-deficient mycobacterial forms also are exclusively RNA. Furthermore, points out Xalabarder, such cell-wall-deficient tubercular forms are true antigens, all of which, similar to Influenza, induce the production of specific antibodies detectable by complement fixation tests, such as those originally used to detect Influenza (5).
CONCLUSION
In a landmark study(15), Dr. Robert Donaldson, working out of the Pathological Society of Great Britain had ruled out that the mycobacteria now referred to as H. Influenza by itself was behind 1918, perhaps because of its disappearing nature. Yet at the same time he quickly added that there wasn't "the slightest shred of evidence" that the disease was due to a "virus" or influenza. Nor was Donaldson ever able to refute Broxmeyer and Noymer's feelings that TB was behind the many deaths in the pandemic, specifically because it is well known that secondary bacterial infections, be they from opportunistic Haemophilus influenza or any other common bacteria, are a common secondary manifestation in TB-infected lungs. During the pandemic, one-third of patients who had Haemophilus influenza were also found to have tuberculosis - keeping in mind, as always, that many other cases with TB went undiagnosed.
In order to understand why we have this emphasis by those virologists invested in a 'killer flu' in the US today, one must look back historically at the science itself. Until the late 1940s influenza 'viruses' were studied as infections, which, although filterable, were conceived of as analogous to bacteria, a kind of ultra or viral-like bacteria. Not to be deterred, and still seeing Influenza as a great opportunity for virology, in 1941 virologist Hirst claimed that influenza ''virus'' could agglutinate (or clot) red blood cells of fowl and other animal species(16). Such a hemagglutinin discovery, in turn, led to fast assays of what is thought to be Influenza. The "H" in H1N1 comes to us through Hirst, who showed that ''virus'' particles first adsorbed to the red cells and, after a certain time, eluted again as a result of what could be interpreted as an enzymatic reaction. But 6 years later, Middlebrook and Dubos(17) made this seem nothing more than a cheap hat trick by showing that similarly red blood cell agglutination could be produced by sera from patients with tuberculosis. Takahashi and Ono(18,19) reviewed similar red cell agglutination occurring in the presence of tuberculous serums.
As Influenza historian van Helvoort aptly pointed out (20), indeed, in the 1930s and 1940s the concept of 'filterable viruses', including Influenza, were subject to such criticism that Virology's very foundations were threatened. Dogmatized statements like those coming from pioneer virologist Andre Lwoff in 1957 : ''Viruses should be considered as viruses because viruses are viruses''(21) were totally unacceptable, and did little to help the situation. So it was in 1952 that Cornelius P. Rhoads, Director of Sloan-Kettering Institute for Cancer Research in New York City, remarked in a conference introduction that the term ''viruses'', such as that of Influenza, had achieved ''a high professional status with doubtful credentials''(22).
Perhaps in his authoritative text, The Pathogenesis of Tuberculosis, Johns Hopkin's head of pathology, Arnold Rich summed things up best:
"In relation to the question of the effect of influenza upon tuberculosis, it should be pointed out that in many cases in which pulmonary tuberculosis has been thought to have followed an attack of influenza it is altogether probable that the supposed attack of influenza was, in reality, a manifestation of an existing tuberculous infection; for tuberculoprotein, whether absorbed from a spreading lesion or injected into the body, can cause constitutional symptoms (fever, malaise, headache, joint pains, anorexia, prostration) quite like those of influenza." (23)
As Professor Hans Rosling ( http://www.youtube.com/watch?v=V8bUtbODV-Q http://www.youtube.com/watch?v=V8bUtbODV-Q) has so aptly pointed out: during the initial 13 days that WHO started gaining data on Swine Flu Deaths, April 24-May 06, 2009, 31 people died of Swine Flu. 29 of these were in Mexico and 2 in the US. During this same 13 day window, 63,000 people, around the world died of tuberculosis. (http://www.who.int/research/en).
What we have today, is a pandemic with "flu-like" symptoms. And flu-like symptoms doesn't necessarily mean "Influenza" is its underlying cause.
Readers interested in the subject of Influenza/TB can also go to Dr. Ron Paul, MD's take at: HYPERLINK "http://informationclearinghouse.info/article22507.htm \\ _blank"http://informationclearinghouse.info/article22507.htm
Other relevant links include:also applicable to the current Swine Flu epidemic include: (http://www.frequencyfoundation.com/2009/07/bird-flu-influenza-and-1918-case-for.html)
And:
(http://www.frequencyfoundation.com/2009/07/swine-flu-do-we-really-have-right.html#links)
REFERENCES
1. Talay F Kumbetli S Altin S Factors associated with Treatment Success for Tuberculosis Patients: a Single Center's Experience in Turkey Jpn. J. Infect. Dis., 61,25-30, 2008.
2. DM Morens et al. Predominant role of bacterial pneumonia as a cause of death in pandemic influenza: Implications for pandemic influenza preparedness. The Journal of Infectious Diseases DOI: 10.1086/591708 (2008).
3. Talbot EA Moore M McCray E Binkin NJ Tuberculosis Among Foreign-Born Persons in the United States, 1993-1998 JAMA. 2000;284:2894-2900.
4. Broxmeyer L. Bird flu, influenza and 1918: The case for mutant Avian tuberculosis. Med Hypotheses. 2006;67(5):1006-15. Epub 2006 Jun 27
5. Xalabardar C, Formas L. Publicaciones Del Instituto Antituberculoso Francisco Moragas. 7, Barcelona; 1970. p. 183.
6. Noymer A, Garenne M. The 1918 influenza epidemic's effects on sex differentials in mortality in the United States. Popul Dev Rev 2000;26(3):56581.
7. Chester FD A Manuel of Determinative Bacteriology Macmillan & Company Ltd, London 1901 p.351. 401ppgs.
8. Stengel A Fox H A text-book of Pathology 6th Edition Philadelphia and London WB Saunders & Co 1915 1039 ppgs P298
9. Smith W, Andrewes C, Laidlaw P. A virus obtained from influenza patients. Lancet 1933;2:6668.
10. Crofton WM The True Nature of Viruses 2nd Edition, Staple Press, London 166pgs 1939
11. (Balan V.F. (1991): The use of chicken embryos for the culture of L-forms of mycobacteria tuberculosis . Problemy Tuberkuleza i Bolezni Legkikh, 2, 5960.)
12. Corper HC. In discussion following mutation forms of the tubercle bacillus. JAMA 1926; 9(October):121011.
13. Burnet F. Filamentous forms of influenza virus. Nature1956; 177(4499):130.
14. Burnet F. Virology as an independent science. Med J Australia 1953; 40(223):8415.
15. Donaldson R. The bacteriology of influenza: with special reference to Pfeiffer's Bacillus. In: Crookshank, editor. Influenza. London: Heinemann; 1922. p. 139313. 144.
16. Hirst GK. The agglutination of red cells by allantoic fluid of chick embryo infected with influenza virus. Science ;xciv:223. 1941.
17. Pound A. Observation on the agglutination and haemolysis of red cells treated with extracts of Mycobacterium tuberculosis: an evaluation of methods. J Pathol Bacteriol 1952;64(1):13143.
18. Takahashi Y, Ono K. Hemagglutination reaction by the phosphatides of the tubercle bacillus. Kekkaku no Kenkyu (Tuberculosis Res) 1957;7:1.
19. Takahashi Y, Ono K. Study on the passive hem agglutination reaction by the phosphate of M. tuberculosis. 1. The reaction and its specificity. Am Rev Resp Dis 1961;83(2):
20. van Helvoort T. History of virus research in the 20th century: the problem of conceptual continuity. Hist Sci1994;32(2):185235.
21. Lwoff A. The concept of virus. The third Marjory Stephenson Memorial Lecture. J Gener Microbiol 1957;xvii:23953.
22. Rhoads CP. Introduction {to a conference on viruses as causative agents in cancer}. Ann NY Acad Sci 1952;liv:8723.
23. Rich, AR The Pathogenesis of Tuberculosis 2nd Printing. Charles C. Thomas Publisher. Springfield, Illinois 1946. 1008 pps.P.627
Lawrence Broxmeyer, MD
Whitestone, New York 11357
nyinstituteofmedicalresearch@yahoo.com
The current Swine "flu" pandemic began in La Gloria, a pig-farming village in the Veracruz mountains of Mexico. Surely, if any place could unlock the true nature of the cause of the 2009 Pandemic, it would be found in La Gloria, whose villagers were certain that they were sickened by the surrounding pig farms, which they accused of polluting their air and water with pig waste. This is much like what happened in Haskell County, Kansas in 1918, original site of the Great Influenza Pandemic of 1918.
But Enrique Sanchez, top official from Mexico's Agriculture Department, could not find H1N1 in mucous samples taken from the pigs several weeks later, on April 30th. Common bacteria were also tested for. However no studies were done to rule out Swine tuberculosis which is predominantly avian and to a lesser extent bovine, and could have also accounted for the wholesale "respiratory" problems the villagers were experiencing.
Mexican health officials, overlooking the La Gloria situation initially, downplayed it, much as health officials everywhere are prone to do. Yet of 43 villagers whose mucous samples were taken, only one, a 5-year-old boy, was confirmed as having Swine Flu. So head investigator from the Biotechnology Institute of the National Autonomous University of Mexico there, Dr. Carlos Arias, told the AP:
"I cannot understand it. I could almost bet that there were more infections related to the virus."
Soon, more than half of La Gloria's 3,000 residents fell ill with FLU-LIKE illness, etiology unknown. 450 of the sickest of these where treated not with anti-virals such as Tamiflu, but with antibiotics and masks. What was the diagnosis handed out? Why it was "acute respiratory infections", and by the time the mucous results came through in early April, most of the villagers had recovered, the more serious cases on antibiotics alone. The "virus" seemed to have left their systems. But the question lingers: since antibiotics don't cure "viruses" what infectious disease in these purported "Influenza" victims had been cured by the antibiotics given?
On June 3rd, 2009 in Global Research, a curious article by F. William Engdahl appeared, entitled "Sarkozy's Secret Plan for Mandatory Swine Flu Vaccination". In it Engdahl plainly stated that "The only problem with the Swine Flu (H1N1) Vaccine, is that to date, neither WHO nor the US Government's Center for Diseases Control (CDC) have succeeded to isolate, photograph with an electron microscope, or chemically classify the H1N1 Influenza A virus". Furthermore there was no scientifically published evidence that French virologists have done so either. Therefore, mentioned Engdahl, "To mandate a vaccination for a putative (supposed or assumed to exist) disease that has never been characterized, is dubious to say the least."
Engdahl had done his homework. When questioned regarding the electron pictograph of H1N1 that the CDC recently came up with on their website, he revealed his source, German virologist Dr Stefan Lanka, an expert on the documentation of viruses, attesting to the fact that the H1N1 picture was bogus. The virologist wrote that he had "written the CDC many times as to who made the H1N1 photo's and whether they where scientifically documented as to chemical characteristics and other properties." There was never any reply. He concluded "If CDC refuses to cite the source of the photos, they are fake." Worse yet he said "The photos are merely liposomes, microscopic artificial sacs whose walls are a double layer of phospholipids, used to carry substances such as drugs, vaccines, and enzymes to specific cells or organs of the body. These have been artificially presented by a process where chick embryos or cell cultures are killed, reduced and then centrifuged with some solvent, to then, in a vacuum, be nanofiltered." As if this wasn't enough, the virologist testified that "Such a structure has never been characterized in either an organism or its fluids. Furthermore, if there wasn't for the centrifuge/solvent/nanofiltration manipulation, not to mention the precipitation procedure, such particles could never be presented under the electron microscope. In conclusion, without the isolation of the H1N1, there is no H1N1 infecting virus"
Engdahl wasn't finished. "Even more bizarre is the admission by the US Government's Food and Drug Administration, an agency responsible for the health and safety of its citizens, that the 'test' approved for premature release to test for H1N1 is not even a proven test. More to the point", continues F. William Engdahl, "there is no forensic evidence in any of the deaths reported to date that has been presented that proves scientifically that any single death being attributed to H1N1 Swine Flu virus was indeed caused by such a virus."
These thoughts were only strengthened when Engdahl looked into "Novavax, a US pharmaceutical company based in Rockville, Maryland, (who) conveniently enough just announced it is developing a vaccine for H1N1 based on 'virus-like particles'".
'Virus-like particles' do not mean virus. Viral-like, cell-wall-deficient forms of tuberculosis, for example, also appear virus-like and apparently.. so also did non-infectious liposomes.
Both the World Health Organization (WHO) and the Centers for Disease Control (CDC) are fully aware of a far more serious and ongoing tuberculosis Pandemic in the world today. Yet they choose to downplay the link, disregarding the similar flu-like symptoms tuberculosis often begins with.
WHO freely admits that there were approximately 1.8 million deaths from tuberculosis in 2007, the most recent year for which data are available as well as that presently about one-third of the world's population, or two billion people, carry the TB bacteria.
The "H" and "N" of influenza sub-typing, revolves around two glycoproteins called Hemagglutin (H) and Neuraminidase (N), both of which can be, and are, associated with infectious diseases such as the minuscule, viral forms of tuberculosis, a disease which ought to be high on the differential diagnosis for 'flu-like illness' . An August, 2008 Medline study in the Journal of Clinical Biochemistry showed that sputum neuraminidase levels over 1.0 mU per mL were proven associated with having tuberculosis in 92% of cases. Previous to this, bacteria closely related to TB were shown, through crystallization, to produce the same protein neuraminidase used to subtype 'Influenza'. Furthermore, as of 2006, it has become obvious in Menozzi's study that similar to Influenza, Tuberculosis not only uses Hemagglutin to attach to the lung's epithelial cells it invades, but requires Hemagglutin for dissemination of the disease to the rest of the body.
Khomenko's 1993 study, showed that the explosive contagiousness of just such influenza-like forms of tuberculosis are exactly the stuff that previous epidemics and pandemics could have been made of. Khomenko was mentioned by Nobel nominee Lida Mattman in her textbook. That is exactly why, that in response to the present world "flu" pandemic, Japan's Health Ministry's Tuberculosis Infection Diseases Control Division deputy director Takeshi Enami went hand in hand with Yoshio Nanba, director of The Office of Pandemic Influenza Preparedness and Response, to attend a news conference in Tokyo on May 1, 2009.
But back in the US, the CDC and NIH seem to feel differently, ignoring everything but "the virus". There was much the same "Influenza" talk when in 1990, a new multi-drug-resistant (MDR) tuberculosis outbreak took place in a large Miami municipal hospital. Soon thereafter, similar outbreaks in three New York City hospitals left many sufferers dying within weeks. By 1992, approximately two years later, drug-resistant tuberculosis had spread to deadly mini-epidemics in seventeen US states, and was reported, not by the American, but the international media, as out of control. Viral forms of swine, avian and human TB can be transmitted from one species to another. By 1993 the World Health Organization (WHO), proclaimed tuberculosis a global health emergency. (1)
1918 AND TODAY
No one can deny the similarities between the onset of the 1918 epidemic and that of today, yet a Press Release, issued on August 19, 2008, by the National Institute of Allergy and Infectious Diseases (NIAID), contains a striking finding and conclusion: The 20 to 40 million deaths worldwide from the great 1918 Influenza ("Flu") Pandemic were NOT due to "flu" or a virus, but to pneumonia caused by massive bacterial infection."(2)
Subsequently, a study published in JAMA by Talbot and Moore (3) in 2000 showed that Mexican immigrants to the US have the highest case rates for tuberculosis among foreign born persons. Mexico is the country where Swine Flu deaths were first documented.
The research of Lawrence Broxmeyer MD (4) first proclaimed that the 1918 pandemic was due to bacteria, particularly mutant forms of flu-like fowl, swine, bovine, and human tuberculosis (TB) bacteria:
( http://drbroxmeyer.netfirms.com/001pdfBIRDFLUEDITORIALPUBLISHED.pdf ).
These forms of tuberculosis are often viral-like, mutate frequently and can "skip" from one species to another. Moreover the antibodies from such viral TB forms react in the compliment fixation and later "viral" assays (5). They also grow on cultures which are supposed to grow only viruses.
In a supportive 16-page-paper which appeared in Population and Development Review, University of California demographers Andrew Noymer and Michael Garenne came up with convincing statistics showing that undetected tuberculosis may have been the real killer in the 1918 flu epidemic (6).
THE ROOTS OF HISTORY
Noymer's TB hypothesis stands sound against history. Few flu "experts" are aware that in medical texts printed circa 1918 "Influenza" was attributed not to a virus but a bacteria called Mycobacterium influenzae, discovered by Pfeiffer and Canon (7) in 1892......not exactly a coincidence since Richard Pfeiffer worked, at one time, for Robert Koch, the discoverer of tuberculosis, a disease also caused by another bacillus called Mycobacterium tuberculosis. Both mycobacteria stained best with carbol-fuchsin, a bacterial stain commonly used in the staining of mycobacteria as it has an affinity for the mycolic acids found in their cell walls. Mycobacteria such as tuberculosis are particularly deadly because they share properties of the fungi ("myco-") as well as bacteria. TB was, not all that long ago, referred to as "captain of the men of death". And it never lost its potential to kill.
Mycobacterium influenzae was considered by most to be the cause of influenza until 1933. But there were serious diagnostic problems with Mycobacterium influenza. Stengel and Fox warned (8) about them in their widely quoted W.B. Saunder's 1915 version of "A Textbook of Pathology". Problems with identification revolved mainly in that although the bacterial influenza occurred abundantly in the sputum of flu patients at first, it decreased in quantity as the cases advanced. And when purulent expectoration stopped, whether the disease was still active or not, Mycobacterium influenzae "disappears entirely"(8).
In 1933 English physicians Wilson Smith, Christopher H. Andrewes, and Patrick P. Laidlaw(9) removed secretions from the throat of a humans with flu-like symptoms thought to have "influenza", and then filtered out a suspected infectious agent, which by virtue of the fact that it went through a filter was falsely proclaimed, from the onset, to be "a virus". Injecting it into ferrets, the ferrets then developed the same flu-like symptoms which Smith, Andrews and Laidlaw summarily declared as "influenza". In addition Sir Christopher Andrewes suggested, with the help of Burnet and Bang, that the term "myxovirus", meaning "mucous virus", be incorporated into a family name for the Influenzas. This, one imagines, was because the organism came from mucous secretions.
But to government pathologist and pioneer physician/researcher William M. Crofton, who by virtue of his office as County pathologist had examined some of Laidlaw's human "Flu" samples, Laidlaw's entire study was flawed. Crofton found Laidlaw's Flu samples to be laced with the bacillus Mycobacteria influenzae, which by then had been renamed Haemophilus Influenzae. To Crofton this bacilli was the common denominator for the Pandemic of 1918 he had witnessed, although the bacteria could be accompanied by an array of opportunistic organisms such as Staph and Strep. Crofton publically and personally confronted and challenged Laidlaw to come to his laboratory for the proof that his Influenza samples weren't viral. Crofton was convinced by the confirmation of scientists like Calmette at Pasteur regarding how certain forms of tuberculosis, appearing both minuscule and viral, could pass through the smallest of filters. Crofton himself then established that tuberculosis could disappear into tissues as viruses did, and then go through filters which stopped cold even most of those "now invariably called viral disease". "Surely, then", Crofton concluded, "Tuberculosis has more right to be considered a true virus than these(10)." So, at a time when viral forms of TB where scantily being documented, Crofton struggled to link H. Flu with the TB it so often infected in coordination with, as historical and political momentum carried Laidlaw's study through for posterity. A great opportunity was missed to correct the record.
Frank Macfarlane Burnet was the first to grow "Influenza" in a laboratory setting; in 1940 he grew influenza in embryonated chicken eggs, using the allantoic sac. He obviously considered such a technique "Influenza" specific, never bothering to consider that such an allantoic site might also be an excellent site for culturing the viral or Cell-Wall-Deficient (CWD) forms of tuberculosis and the mycobacteria. Viral TB, in fact grows there as early as 6 hours after introduction into such a place in chicken embryos(11).
Furthermore, some of the filamentous forms of tuberculosis mentioned by Corper (12) appear similar to those attributed to ''Influenza'' by biochemist and Influenza guru Burnet (13).
It wasn't because Burnet didn't know that bacteria could assume viral forms. The first, and for a time the only virologist in Australia, it was Burnet who discovered bacteria in viral forms of Q-fever (14). And in that same paper, proclaiming Virology as an Independent Science , and after admitting that viruses, including influenza, are composed of the same sorts of material as bacteria, Burnet struggles to differentiate Influenza by the fact that it ''probably has no DNA'' and was therefore exclusively RNA.(Ibid.). But, according to Xalabardar, some cell-wall-deficient mycobacterial forms also are exclusively RNA. Furthermore, points out Xalabarder, such cell-wall-deficient tubercular forms are true antigens, all of which, similar to Influenza, induce the production of specific antibodies detectable by complement fixation tests, such as those originally used to detect Influenza (5).
CONCLUSION
In a landmark study(15), Dr. Robert Donaldson, working out of the Pathological Society of Great Britain had ruled out that the mycobacteria now referred to as H. Influenza by itself was behind 1918, perhaps because of its disappearing nature. Yet at the same time he quickly added that there wasn't "the slightest shred of evidence" that the disease was due to a "virus" or influenza. Nor was Donaldson ever able to refute Broxmeyer and Noymer's feelings that TB was behind the many deaths in the pandemic, specifically because it is well known that secondary bacterial infections, be they from opportunistic Haemophilus influenza or any other common bacteria, are a common secondary manifestation in TB-infected lungs. During the pandemic, one-third of patients who had Haemophilus influenza were also found to have tuberculosis - keeping in mind, as always, that many other cases with TB went undiagnosed.
In order to understand why we have this emphasis by those virologists invested in a 'killer flu' in the US today, one must look back historically at the science itself. Until the late 1940s influenza 'viruses' were studied as infections, which, although filterable, were conceived of as analogous to bacteria, a kind of ultra or viral-like bacteria. Not to be deterred, and still seeing Influenza as a great opportunity for virology, in 1941 virologist Hirst claimed that influenza ''virus'' could agglutinate (or clot) red blood cells of fowl and other animal species(16). Such a hemagglutinin discovery, in turn, led to fast assays of what is thought to be Influenza. The "H" in H1N1 comes to us through Hirst, who showed that ''virus'' particles first adsorbed to the red cells and, after a certain time, eluted again as a result of what could be interpreted as an enzymatic reaction. But 6 years later, Middlebrook and Dubos(17) made this seem nothing more than a cheap hat trick by showing that similarly red blood cell agglutination could be produced by sera from patients with tuberculosis. Takahashi and Ono(18,19) reviewed similar red cell agglutination occurring in the presence of tuberculous serums.
As Influenza historian van Helvoort aptly pointed out (20), indeed, in the 1930s and 1940s the concept of 'filterable viruses', including Influenza, were subject to such criticism that Virology's very foundations were threatened. Dogmatized statements like those coming from pioneer virologist Andre Lwoff in 1957 : ''Viruses should be considered as viruses because viruses are viruses''(21) were totally unacceptable, and did little to help the situation. So it was in 1952 that Cornelius P. Rhoads, Director of Sloan-Kettering Institute for Cancer Research in New York City, remarked in a conference introduction that the term ''viruses'', such as that of Influenza, had achieved ''a high professional status with doubtful credentials''(22).
Perhaps in his authoritative text, The Pathogenesis of Tuberculosis, Johns Hopkin's head of pathology, Arnold Rich summed things up best:
"In relation to the question of the effect of influenza upon tuberculosis, it should be pointed out that in many cases in which pulmonary tuberculosis has been thought to have followed an attack of influenza it is altogether probable that the supposed attack of influenza was, in reality, a manifestation of an existing tuberculous infection; for tuberculoprotein, whether absorbed from a spreading lesion or injected into the body, can cause constitutional symptoms (fever, malaise, headache, joint pains, anorexia, prostration) quite like those of influenza." (23)
As Professor Hans Rosling ( http://www.youtube.com/watch?v=V8bUtbODV-Q http://www.youtube.com/watch?v=V8bUtbODV-Q) has so aptly pointed out: during the initial 13 days that WHO started gaining data on Swine Flu Deaths, April 24-May 06, 2009, 31 people died of Swine Flu. 29 of these were in Mexico and 2 in the US. During this same 13 day window, 63,000 people, around the world died of tuberculosis. (http://www.who.int/research/en).
What we have today, is a pandemic with "flu-like" symptoms. And flu-like symptoms doesn't necessarily mean "Influenza" is its underlying cause.
Readers interested in the subject of Influenza/TB can also go to Dr. Ron Paul, MD's take at: HYPERLINK "http://informationclearinghouse.info/article22507.htm \\ _blank"http://informationclearinghouse.info/article22507.htm
Other relevant links include:also applicable to the current Swine Flu epidemic include: (http://www.frequencyfoundation.com/2009/07/bird-flu-influenza-and-1918-case-for.html)
And:
(http://www.frequencyfoundation.com/2009/07/swine-flu-do-we-really-have-right.html#links)
REFERENCES
1. Talay F Kumbetli S Altin S Factors associated with Treatment Success for Tuberculosis Patients: a Single Center's Experience in Turkey Jpn. J. Infect. Dis., 61,25-30, 2008.
2. DM Morens et al. Predominant role of bacterial pneumonia as a cause of death in pandemic influenza: Implications for pandemic influenza preparedness. The Journal of Infectious Diseases DOI: 10.1086/591708 (2008).
3. Talbot EA Moore M McCray E Binkin NJ Tuberculosis Among Foreign-Born Persons in the United States, 1993-1998 JAMA. 2000;284:2894-2900.
4. Broxmeyer L. Bird flu, influenza and 1918: The case for mutant Avian tuberculosis. Med Hypotheses. 2006;67(5):1006-15. Epub 2006 Jun 27
5. Xalabardar C, Formas L. Publicaciones Del Instituto Antituberculoso Francisco Moragas. 7, Barcelona; 1970. p. 183.
6. Noymer A, Garenne M. The 1918 influenza epidemic's effects on sex differentials in mortality in the United States. Popul Dev Rev 2000;26(3):56581.
7. Chester FD A Manuel of Determinative Bacteriology Macmillan & Company Ltd, London 1901 p.351. 401ppgs.
8. Stengel A Fox H A text-book of Pathology 6th Edition Philadelphia and London WB Saunders & Co 1915 1039 ppgs P298
9. Smith W, Andrewes C, Laidlaw P. A virus obtained from influenza patients. Lancet 1933;2:6668.
10. Crofton WM The True Nature of Viruses 2nd Edition, Staple Press, London 166pgs 1939
11. (Balan V.F. (1991): The use of chicken embryos for the culture of L-forms of mycobacteria tuberculosis . Problemy Tuberkuleza i Bolezni Legkikh, 2, 5960.)
12. Corper HC. In discussion following mutation forms of the tubercle bacillus. JAMA 1926; 9(October):121011.
13. Burnet F. Filamentous forms of influenza virus. Nature1956; 177(4499):130.
14. Burnet F. Virology as an independent science. Med J Australia 1953; 40(223):8415.
15. Donaldson R. The bacteriology of influenza: with special reference to Pfeiffer's Bacillus. In: Crookshank, editor. Influenza. London: Heinemann; 1922. p. 139313. 144.
16. Hirst GK. The agglutination of red cells by allantoic fluid of chick embryo infected with influenza virus. Science ;xciv:223. 1941.
17. Pound A. Observation on the agglutination and haemolysis of red cells treated with extracts of Mycobacterium tuberculosis: an evaluation of methods. J Pathol Bacteriol 1952;64(1):13143.
18. Takahashi Y, Ono K. Hemagglutination reaction by the phosphatides of the tubercle bacillus. Kekkaku no Kenkyu (Tuberculosis Res) 1957;7:1.
19. Takahashi Y, Ono K. Study on the passive hem agglutination reaction by the phosphate of M. tuberculosis. 1. The reaction and its specificity. Am Rev Resp Dis 1961;83(2):
20. van Helvoort T. History of virus research in the 20th century: the problem of conceptual continuity. Hist Sci1994;32(2):185235.
21. Lwoff A. The concept of virus. The third Marjory Stephenson Memorial Lecture. J Gener Microbiol 1957;xvii:23953.
22. Rhoads CP. Introduction {to a conference on viruses as causative agents in cancer}. Ann NY Acad Sci 1952;liv:8723.
23. Rich, AR The Pathogenesis of Tuberculosis 2nd Printing. Charles C. Thomas Publisher. Springfield, Illinois 1946. 1008 pps.P.627
Lawrence Broxmeyer, MD
Whitestone, New York 11357
nyinstituteofmedicalresearch@yahoo.com
Tuesday, October 27, 2009
WHO memos 1972 explains how to turn vaccines into a means of killing
Two key memorandums from WHO, discovered by Patrick Jordan, prove WHO has intentionally created the three-shot killer vaccine that people in the USA and other countries could soon be forced to take.
1972 WHO Bulletin 47, No 2 Memordanda #1 and #2 Virus-associated immunopathology:
Animal models and implications for human disease * technically outline the ability to create biological weapons in the form of vaccines that:
1) First totally disable the Immune System.
2) Load every cell of the Victim’s body up with Infection.
3) Switch the Immune System on causing the host to kill themselves in a Cytokine Storm.
One, Two, Three, Dead.
These WHO Memorandas describe the three-stage impact of the three "shots" many people will be forced to take this fall to allegedly treat a virus that WHO also helped create and release.
This is a crucial piece of evidence of WHO's long-term genocidal intentions that could stand in any court of law because these memorandums give the best and fullest explanation WHO's and affiliated labs (such as the CDC) current activities, such as their patenting of the most lethal bird flu viruses, their sending that virus to Baxter's subsidiary in Austria, which weaponised it and sent out 72 kilos to 16 labs in four countries almost triggering a global pandemic.
For every crime, there needs to be motive, an indication that it was deliberate, planned. The WHO memorandums provide the evidence of just that deliberate, long-term planning to kill people by weakening their immune system by use of the first vaccine, injecting a live virus into their body by a second, and creating a cytokine storm using squalene in a third.
Download the WHO Memoranda on:
http://www.pubmedcentral.nih.gov/tocrender.fcgi?iid=169484
Scroll down until you find:
Memoranda
Virus-associated immunopathology : animal models and implications for human disease:
1. Effects of viruses on the immune system, immune-complex diseases, and antibody-mediated immunologic injury
Bull World Health Organ. 1972; 47(2): 257?264.
PMCID: PMC2480894
http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=2480894&blobtype=pdf
Virus-associated immunopathology: animal models and implications for human disease:
2. Cell-mediated immunity, autoimmune diseases, genetics, and implications for clinical research
Bull World Health Organ. 1972; 47(2): 265?274
PMCID: PMC2480896
http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=2480896&blobtype=pdf
1972 WHO Bulletin 47, No 2 Memordanda #1 and #2 Virus-associated immunopathology:
Animal models and implications for human disease * technically outline the ability to create biological weapons in the form of vaccines that:
1) First totally disable the Immune System.
2) Load every cell of the Victim’s body up with Infection.
3) Switch the Immune System on causing the host to kill themselves in a Cytokine Storm.
One, Two, Three, Dead.
These WHO Memorandas describe the three-stage impact of the three "shots" many people will be forced to take this fall to allegedly treat a virus that WHO also helped create and release.
This is a crucial piece of evidence of WHO's long-term genocidal intentions that could stand in any court of law because these memorandums give the best and fullest explanation WHO's and affiliated labs (such as the CDC) current activities, such as their patenting of the most lethal bird flu viruses, their sending that virus to Baxter's subsidiary in Austria, which weaponised it and sent out 72 kilos to 16 labs in four countries almost triggering a global pandemic.
For every crime, there needs to be motive, an indication that it was deliberate, planned. The WHO memorandums provide the evidence of just that deliberate, long-term planning to kill people by weakening their immune system by use of the first vaccine, injecting a live virus into their body by a second, and creating a cytokine storm using squalene in a third.
Download the WHO Memoranda on:
http://www.pubmedcentral.nih.gov/tocrender.fcgi?iid=169484
Scroll down until you find:
Memoranda
Virus-associated immunopathology : animal models and implications for human disease:
1. Effects of viruses on the immune system, immune-complex diseases, and antibody-mediated immunologic injury
Bull World Health Organ. 1972; 47(2): 257?264.
PMCID: PMC2480894
http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=2480894&blobtype=pdf
Virus-associated immunopathology: animal models and implications for human disease:
2. Cell-mediated immunity, autoimmune diseases, genetics, and implications for clinical research
Bull World Health Organ. 1972; 47(2): 265?274
PMCID: PMC2480896
http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=2480896&blobtype=pdf
Friday, October 23, 2009
Thursday, October 22, 2009
The Income Tax Trial of the Century
THE INCOME TAX CASE OF THE CENTURY -- DO YOU EVEN KNOW ABOUT IT?
On Tuesday, October 20th, Pete Hendrickson, author of the bestselling book "Cracking the Code: The Fascinating Truth About Taxation in America" will be tried at the Theodore Levin Courthouse before Judge Gerald Rosen and a Detroit, Michigan jury. Word of the trial has not reached most Americans -- even those who are aware of the so-called fraud of "income" tax.
The charge against Pete is that he didn't believe what he wrote on his tax returns filed between 2002 and 2007. [ Yes, you read it correctly, Pete is charged with NOT BELIEVING WHAT HE WROTE ON HIS RETURNS! ] This is a matter of philosophy -- did he or didn't he? If you or I were asked to answer that question, we would consider the decade Pete has spent researching the 6-plus million words of Internal Revenue Code and statutory law, the ground-breaking book he published about his findings, and the enormous website he has built and maintains, at which one can view the results of hundreds of individual filings made by those who have read Pete's book. What are these results? A total of $10.2 million to date in collective "victories" -- including complete annual refunds of wage withholdings and dismissals of 1099s. (And these are only the victories of those who have reported their successes back to Pete.)
The case against Pete was brought in November 2008 -- a last-ditch massive PR effort on the part of the IRS to blacken Pete's book and frighten people off from reading it. If the writer himself is on trial ... Yet the proof in the pudding is that the whole time Pete has been preparing his defense, the IRS has continued to refund filers applying the liberating truth they are learning from Cracking the Code.
Why is the income-tax community not up in arms about this trial? Why do we not even know about it? Possibly because the "real deal" in any of the issues whirling around us is given the least attention -- by deliberate design.
In my own journey down the road of alternative thinking, I have come to learn (and it only dawned on me very recently) that a certain kind of paradigm is systematically constructed around all of our favorite "conspiracy" topics. I will use the familiar terms thesis, antithesis and synthesis. Pick a topic -- vaccines, for instance. Thesis is what most people believe: "Vaccines are good for you. They protect your health and prevent disease. Vaccinate your child and get your flu shot now." Antithesis is what most conspiracy theorists or mainline skeptics believe, and it is also predominantly false. The antithesis for vaccines is: "Vaccines will kill you! They give you the disease they're supposed to protect against. The swine flu shot will give you swine flu!" The synthesis that nearly everyone misses is quite different -- and the reason no one gets to it is because of all the noise around the other stuff. Synthesis: "Vaccines are likely to cause immune dysfunction and impair your general health. They create chronic ailments, neurological disorders ranging from learning disabilities to full-blown autism, as well as auto-immune disorders. Their net effect is limited functionality."
Look at any subject people are exposing and you will find this spectrum. Thesis, antithesis, synthesis. The beauty of peddling a false antithesis is that the day will come when its believers will be wrong. And the more dis-believers you can draw to the antithesis, the yet-more-people you can fool!
Income tax. Most Americans believe it's unavoidable -- if you make money, you have to pay the government a portion of your earnings. Thesis. It's the law. Antithesis: Income tax is unlawful -- it's unconstitutional! Just don't file, just don't pay! The synthesis is what Pete Hendrickson's research brings us: Income tax is lawful, it's constitutional. It's just a very narrow, benign tax that doesn't apply to the money most people bring in. It's a federal excise tax, not a direct tax -- payable only on money that is federally connected. Why do most people end up paying tax on their "income"? Because of a fraudulent nationwide reporting system, whereby Americans use forms intended only for federally connected payments to advise the IRS of amounts they have paid to each other. The W-2 and 1099 "information returns" subject those whose names appear on them to a tax on their "income," as this word is a LEGAL TERM applying to money that comes from a federal nexus.
Pete's research discloses ways that Americans themselves can rectify the reports made about them, and the IRS accepts these corrections. Thus those employing what Pete calls "Congress's own method" of restitution are consistently succeeding in obtaining a RETURN of their withheld earnings -- which is the intended meaning of the "1040 U.S. Individual Income Tax Return."
It's a beautiful, liberating discovery. The government expanded its "revenue" by imposing a broad income tax upon the people in the early 1940s -- even on those who did not qualify as "taxpayers." Why? We were at war and they needed the funds. They felt it was okay to borrow from our paychecks throughout the year, and we could turn around and ask for the withholdings back by April 15th of the next year. Small increments taken from us on a temporary basis, and then a "return" of our money if we did not qualify as a true "employee," earning "wages." (These, again, are specific legal terms! Read Cracking the Code to educate yourself.)
And for this gift to the American people, Pete Hendrickson is being put into the fire. He may be sentenced to a prison term if he is not able to convince the jury on the correctness and fairness of the law. The real law, the way it was originally and perfectly designed. Which design has been completely drowned out by the noise around the ill-defined thesis (we have to pay) and the equally ill-defined antithesis (we certainly do not).
I ask you to visit www.NotIncome.com and www.LostHorizons.com to learn much, much more. Read Pete's newsletter here (http://www.losthorizons.com/Newsletter.htm) ... and this may be the time to buy Cracking the Code: The Fascinating Truth About Taxation in America. Donate to Pete's enormous cost of legal defense, as he has had to hire the best and brightest to work with him. A victory in this trial could mean a turning point for you and every other American alive today.
Why didn't you know this was going on? Because it's Synthesis -- one of the gems kept hidden from us so we never really know what is at our disposal to help our deep, true, freedom-deserving selves.
On Tuesday, October 20th, Pete Hendrickson, author of the bestselling book "Cracking the Code: The Fascinating Truth About Taxation in America" will be tried at the Theodore Levin Courthouse before Judge Gerald Rosen and a Detroit, Michigan jury. Word of the trial has not reached most Americans -- even those who are aware of the so-called fraud of "income" tax.
The charge against Pete is that he didn't believe what he wrote on his tax returns filed between 2002 and 2007. [ Yes, you read it correctly, Pete is charged with NOT BELIEVING WHAT HE WROTE ON HIS RETURNS! ] This is a matter of philosophy -- did he or didn't he? If you or I were asked to answer that question, we would consider the decade Pete has spent researching the 6-plus million words of Internal Revenue Code and statutory law, the ground-breaking book he published about his findings, and the enormous website he has built and maintains, at which one can view the results of hundreds of individual filings made by those who have read Pete's book. What are these results? A total of $10.2 million to date in collective "victories" -- including complete annual refunds of wage withholdings and dismissals of 1099s. (And these are only the victories of those who have reported their successes back to Pete.)
The case against Pete was brought in November 2008 -- a last-ditch massive PR effort on the part of the IRS to blacken Pete's book and frighten people off from reading it. If the writer himself is on trial ... Yet the proof in the pudding is that the whole time Pete has been preparing his defense, the IRS has continued to refund filers applying the liberating truth they are learning from Cracking the Code.
Why is the income-tax community not up in arms about this trial? Why do we not even know about it? Possibly because the "real deal" in any of the issues whirling around us is given the least attention -- by deliberate design.
In my own journey down the road of alternative thinking, I have come to learn (and it only dawned on me very recently) that a certain kind of paradigm is systematically constructed around all of our favorite "conspiracy" topics. I will use the familiar terms thesis, antithesis and synthesis. Pick a topic -- vaccines, for instance. Thesis is what most people believe: "Vaccines are good for you. They protect your health and prevent disease. Vaccinate your child and get your flu shot now." Antithesis is what most conspiracy theorists or mainline skeptics believe, and it is also predominantly false. The antithesis for vaccines is: "Vaccines will kill you! They give you the disease they're supposed to protect against. The swine flu shot will give you swine flu!" The synthesis that nearly everyone misses is quite different -- and the reason no one gets to it is because of all the noise around the other stuff. Synthesis: "Vaccines are likely to cause immune dysfunction and impair your general health. They create chronic ailments, neurological disorders ranging from learning disabilities to full-blown autism, as well as auto-immune disorders. Their net effect is limited functionality."
Look at any subject people are exposing and you will find this spectrum. Thesis, antithesis, synthesis. The beauty of peddling a false antithesis is that the day will come when its believers will be wrong. And the more dis-believers you can draw to the antithesis, the yet-more-people you can fool!
Income tax. Most Americans believe it's unavoidable -- if you make money, you have to pay the government a portion of your earnings. Thesis. It's the law. Antithesis: Income tax is unlawful -- it's unconstitutional! Just don't file, just don't pay! The synthesis is what Pete Hendrickson's research brings us: Income tax is lawful, it's constitutional. It's just a very narrow, benign tax that doesn't apply to the money most people bring in. It's a federal excise tax, not a direct tax -- payable only on money that is federally connected. Why do most people end up paying tax on their "income"? Because of a fraudulent nationwide reporting system, whereby Americans use forms intended only for federally connected payments to advise the IRS of amounts they have paid to each other. The W-2 and 1099 "information returns" subject those whose names appear on them to a tax on their "income," as this word is a LEGAL TERM applying to money that comes from a federal nexus.
Pete's research discloses ways that Americans themselves can rectify the reports made about them, and the IRS accepts these corrections. Thus those employing what Pete calls "Congress's own method" of restitution are consistently succeeding in obtaining a RETURN of their withheld earnings -- which is the intended meaning of the "1040 U.S. Individual Income Tax Return."
It's a beautiful, liberating discovery. The government expanded its "revenue" by imposing a broad income tax upon the people in the early 1940s -- even on those who did not qualify as "taxpayers." Why? We were at war and they needed the funds. They felt it was okay to borrow from our paychecks throughout the year, and we could turn around and ask for the withholdings back by April 15th of the next year. Small increments taken from us on a temporary basis, and then a "return" of our money if we did not qualify as a true "employee," earning "wages." (These, again, are specific legal terms! Read Cracking the Code to educate yourself.)
And for this gift to the American people, Pete Hendrickson is being put into the fire. He may be sentenced to a prison term if he is not able to convince the jury on the correctness and fairness of the law. The real law, the way it was originally and perfectly designed. Which design has been completely drowned out by the noise around the ill-defined thesis (we have to pay) and the equally ill-defined antithesis (we certainly do not).
I ask you to visit www.NotIncome.com and www.LostHorizons.com to learn much, much more. Read Pete's newsletter here (http://www.losthorizons.com/Newsletter.htm) ... and this may be the time to buy Cracking the Code: The Fascinating Truth About Taxation in America. Donate to Pete's enormous cost of legal defense, as he has had to hire the best and brightest to work with him. A victory in this trial could mean a turning point for you and every other American alive today.
Why didn't you know this was going on? Because it's Synthesis -- one of the gems kept hidden from us so we never really know what is at our disposal to help our deep, true, freedom-deserving selves.
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