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This was a very interesting documentary in that is shows documents that explain the planning of this virus by the US government and that there is a patent cure already listed as #5677977. How the worst virus to ever arrive on earth erupts on two continents are the same time is problem number 1. The fact that there is a patent cure which has not been released is problem 2.
How many has this virus killed already? Millions is the answer. It's eugenics at it's best or worse if you think as I do.
I went to uspto.gov and did a search on that patent number. This is what I got. It says it's an abandoned patent.
http://patft.uspto.gov/netacgi/nph-P...&RS=PN/5676977
This was some of the info shared:
United States Patent 5,676,977 Antelman October 14, 1997 Method of curing AIDS with tetrasilver tetroxide molecular crystal devices
Abstract The diamagnetic semiconducting molecular crystal tetrasilver tetroxide (Ag.sub.4 O.sub.4) is utilized for destroying the AIDS virus, destroying AIDS synergistic pathogens and immunity suppressing moieties (ISM) in humans. A single intravenous injection of the devices is all that is required for efficacy at levels of about 40 PPM of human blood. The device molecular crystal contains two mono and two trivalent silver ions capable of "firing" electrons capable of electrocuting the AIDS virus, pathogens and ISM. When administered into the bloodstream, the device electrons will be triggered by pathogens, a proliferating virus and ISM, and when fired will simultaneously trigger a redox chelation mechanism resulting in divalent silver moieties which chelate and bind active sites of the entities destroying them. The devices are completely non-toxic. However, they put stress on the liver causing hepatomegaly, but there is no loss of liver function.
Inventors: Antelman; Marvin S. (Rehovot, IL) Assignee: Antelman Technologies Ltd. (Providence, RI)
Appl. No.: 08/658,955 Filed: May 31, 1996
What is claimed is:
1. A method of treating AIDS-afflicted humans comprising injecting a multitude of tetrasilver tetroxide molecular crystals into the bloodstream of the human subject.
2. A method for increasing white blood cell counts in AIDS-afflicted humans comprising injecting a multitude of tetrasilver tetroxide molecular crystals into the bloodstream of the human subject.
3. Methods of treating AIDS-affilicted humans according to claims 1-2 where the concentration of said molecular crystals is approximately 40 PPM of the total blood weight of the human subject. Description
BACKGROUND OF THE INVENTION
The present invention relates to the employment of molecular crystals as anti-AIDS devices, but more particularly to the molecular crystal semiconductor tetrasilver tetroxide Ag.sub.4 O.sub.4 which has two monovalent and two trivalent silver ions per molecule, and which through this structural configuration enables intermolecular electron transfer capable of killing viruses and binding them to the resulting silver entity so that a single intravenous injection will completely obliterate acquired immune deficiency syndrome (AIDS) in humans. Furthermore, said devices are capable of killing pathogens and purging the bloodstream of immune suppressing moieties (ISM) whether or not created by the AIDS virus (HIV); so as to restore the immune system.
The present invention is based on concepts previously elucidated in applicant's U.S. Pat. No. 5,336,499 which discloses the destruction and inhibition of bacteria, algae and the AIDS virus in nutrient life supporting systems by using said silver oxide devices. Example 3 of said patent discloses that 18 PPM of said crystal devices could totally suppress the AIDS virus (page 6, line 5). Subsequent to the filing of the aforementioned patent, further testing revealed complete 100% destruction of the AIDS virus in vitro at 20 PPM, and the fact that said devices were harmless when ingested and inhaled, being non-toxic.
Encouraged by these evaluations and successes, applicant obtained permission to evaluate the crystals in vitro against murine acquired immune deficiency syndrome (MAIDS). Only one facility in the State of Israel is licensed for these evaluations, namely, the Kaplan Hospital in Rehovot, Israel, which is affiliated with the Hebrew University-Hadassah Medical School where said evaluations were done.
The initial evaluations entailed experimenting with various silver moieties cited in applicant's aforementioned patent, concentrations, non-reactive buffers and modes of administration. After about 18 months of judicious efforts and initial failures, success was finally achieved in destroying the MAIDS virus in C57BL mice with a single intravenous injection. The results of this test program comprise Example 5 of U.S. Pat. No. 5,336,499. After success with mice, the inventor was able to test the efficacy of said devices on two select etiological groups of terminal AIDS patients in a clinic in Tegucigalpa, Honduras, Central America.
The AIDS patients comprised the etiological subgroups, Candidiasis and Wasting Syndrome. Current indicator diseases for diagnosing AIDS which have been expanded by the CDC, fall into the following five major categories with the approximate percent distribution among AIDS patients:
______________________________________ 1. P. carinii pneumonia 51% 2. Wasting syndrome 19% 3. Candidiasis 13% 4. Kaposi's sarcoma 11% 5. Dementia 6% ______________________________________
This invention concerns itself with the treatment and cure of candidiasis and wasting syndrome AIDS patients with Tetrasil*. These two groups account for approximately one third of AIDS cases.
Stedman's Medical Dictionary (Williams & Wilken's 26th Ed., 1995) defines wasting syndrome "as a condition of 10% weight loss in conjunction with diarrhea or fever . . . Associated with AIDS (p. 1744)."
OBJECTS OF THE INVENTION
The main object of the invention is to provide for a molecular scale device of a single tetrasilver tetroxide crystalline molecule capable of restoring the immunity of AIDS afflicted humans of the two AIDS etiological subgroups, candidiasis and wasting syndrome.
Another object of the invention is to provide for immunity restoration in said AIDS afflicted humans through a single injection.
Another object of this invention is to destroy ISM in humans manifesting AIDS diseases of said AIDS etiological subgroups irrespective as to whether said ISM was HIV induced, since it is known that humans may manifest AIDS and still be HIV negative, and thus restore the immune system in said humans.
Another object of this invention is to destroy the AIDS virus when present in the systems of said AIDS afflicted humans.
SUMMARY OF THE INVENTION
This invention relates to a molecular scale device not only capable of destroying the AIDS virus, but of purging the human bloodstream of pathogens and restoring immunity to AIDS patients of the candidiasis and wasting syndrome categories. Said molecular device consists of a single crystal of tetrasilver tetroxide (Ag.sub.4 O.sub.4). The crystal lattice of this molecule has a unique structure since it is a diamagnetic semiconducting crystal containing two mono and two trivalent silver ions, which in effect are capable of "firing" electrons under certain conditions which will destroy AIDS viruses, other pathogens and immune suppressing moieties (ISM), not only through the electrocution mode, but also by a binding process which occurs simultaneously with electron firing, namely, binding and chelation of divalent silver, i.e., the resulting product of the electron transfer redox that occur when the monovalent silver ions are oxidized and the trivalent ions are reduced in the crystal. The binding/chelation effect occurs at active sites of the AIDS virus, pathogens and ISM. Because of the extremely minute size of a single molecule of this crystal, several million of these devices may be employed in concert to destroy a virus colony to purge a life support system of ISM and pathogens with the consumption of only parts per trillion of the crystal devices. Thus an optimum of 40 PPM of the devices by weight of human blood was found to be sufficient to completely obliterate AIDS. This concentration is slightly over double of the optimum concentration recommended in applicant's aforementioned U.S. patent for the destruction of the human AIDS virus in vitro. Other details concerning the structure of the crystal and its mechanism against pathogens, the AIDS virus and ISM would analogously hold here, and have already been further elucidated in said patent.
The actual destruction of pathogens, ISM and the AIDS virus is effectuated by injection of a suspension of these devices in distilled or deionized water with a non-reacting electrolyte directly, i.e. intravenously, into the bloodstream. A single injection is all that is required under these conditions. Accordingly, humans injected in this manner, upon being inspected after three weeks or more had elapsed and compared with similar humans that had been given placebos, were completely cured of AIDS. The control group still manifested AIDS. Accordingly, the tetrasilver tetroxide device performed in concert with and in full conformity with the ultimate objects of this invention. Furthermore, three out of four wasting syndrome terminal patients and four out of the five candidiasis terminal patients were still alive in 1995 after a year and a half had elapsed from their initial injection. By that time all the AIDS patients had been released from the clinic and allowed to return home.
Other objects and features of the present invention shall become apparent to those skilled in the art when the present invention is considered in view of the accompanying examples. It should, of course, be recognized that the accompanying examples illustrate preferred embodiments of the present invention and are not intended as a means of defining the limits and scope of the present invention.
EXAMPLE 1
Five patients afflicted with AIDS of the candidiasis etiological category were segregated for Tetrasil treatment. The rationale for selecting them was based on facts presented in an article by Peter H. Duesberg and Brian J. Ellison entitled "Is The AIDS Virus A Science Fiction?" (Policy Review, Summer 1990 pp. 40-51). Only the factual presentations of the article were utilized and the hypothesis of the authors was ignored. The facts presented in the article related to the method of selecting AIDS patients based on the five aforementioned etiological subgroups targeted by the CDC, and the evidence presented, that there is AIDS without HIV as well as with it so that an anti-viral agent in most instances will not necessarily restore the immunity system.
Evaluations with Tetrasil were conducted on AIDS patients at Lucha Contra el Sida, Comayaguela, Honduras. The patients two weeks prior to inoculation were removed from their AZT, AIDS therapy. Tetrasil was administered at approximately 40 PPM of blood volume per patient as a suspension in a proprietary buffer solution (pH=6.5), supplied by Holipharm Corporation.
The results of evaluations with candidiasis are tabulated in Table I under its disease category. All patients evaluated were terminal. Some, however, were in moderate (m) condition and others in poor (p) as designated in the Table. The I and F designations refer to initial and final values as shown. WBC indicates white cell blood count. The H column, following CD 8, indicates whether hepatomegaly occurred. This was an unfortunate consequence of the treatment which resulted in enlarged livers in all patients except the second one. Despite hepatomegaly, there was no interference with liver function.
The onset of hepatomegaly was not spontaneous and varied from patient to patient, being in the range of 4-16 days.
It should also be noted that shortly after injection of Tetrasil there were indications of fever (symbolized by T in the Ag.sub.4 O.sub.4 column), sometimes accompanied by fatigue (F). The body temperature was invariably 38.5.degree. C. (101.3.degree. F.). This was indicative of restoration of the immune response of the body, since normally the body will destroy pathogens when the immune system is functional by raising the temperature. The patient who died; first responded favorably to Diflucan, which previously gave no response. He was cured of his candidiasis, but unfortunately succumbed to his previous body damage. All the other candidiasis syndrome people who previously did not respond to the indicated medications subsequently responded after the Tetrasil treatment. Further evidence of the recovery of the AIDS patients manifested itself 30 days after the initial injection when white blood cell counts were taken. They are shown in Table I under the WBC column, which gives the initial and final WBC. All candidiasis patients showed a dramatic increase in their white blood cell counts, indicative of the restoration of their immunity systems.
EXAMPLE 2
The above protocol of Example 1 was repeated with AIDS patients exhibiting wasting syndrome. The results of their treatment are tabulated in Table I under the disease category of said syndrome. It should be noted that two of the four wasting syndrome patients showed improved white blood counts. The female patient, whose condition improved from poor and terminal to be among the living, showed a decrease in the WBC. However, she showed an increase in body temperature which was indicative of immune response. The test results indicate that one cannot rely on a single factor to indicate the demise of AIDS. The usual HIV marker CD 4 initial and final are irrelevant. ISM suppression appears to be more critical than the destruction of HIV. AIDS was suppressed, any permanent damage that had been done to the patients in the course of their succumbing to AIDS was not obviously cured or corrected by said crystal device treatment, rather said injury persisted and the patient was improved with respect to AIDS but still suffered from said permanent injury or impairment previously inflicted.
United Serenity, here you go again.
We haven't gotten rid of all the gays and the Africans on that valuable land and anyone and everyone else that stand in the way of a perfectly ordered world.
We have tp prove to you that the earth and nature are dangerous and that we need to vaccinate you against it.
HIV is the wrath of God. Shut up and accept it.
Here is the flow chart and notes from www.boydgraves.com
Click the image to download the chart
http://www.boydgraves.com/images/flowchart.gif
The Smoking Gun of AIDS: a 1971 Flowchart
by Boyd E. Graves, J.D.
December 6, 2000
In 1977, a secret federal virus program produced 15,000 gallons of AIDS. The record reveals the United States was represented by Dr. Robert Gallo and the USSR was represented by Dr. Novakhatsky of the diabolical Ivanosky Institute. On August 21, 1999, the world first saw the flowchart of the plot to thin the Black Population.
The 1971 AIDS flowchart coordinates over 20,000 scientific papers and fifteen years of progress reports of a secret federal virus development program. The epidemiology of AIDS is an identical match to the "research logic" identified in the five section foldout. The flowchart is page 61 of Progress Report #8 (1971) of the Special Virus program of the United States of America. We today, challenge world scientists to discussion of this document find.
We believe there is a daily, growing number of world experts who are all coming to the same conclusion regarding the significance of the flowchart. Dr. Garth Nicolson has examined the flowchart as well as other top experts from around the world. It is time for Dr. Michael Morrissey of Germany to examine the flowchart and report to the world. In addition, we have now examined the 1978 report. It is heresy to continue to further argue the program ended in 1977.
The 1978 report of the development of AIDS leaves no doubt as to the ("narrow result") candidate virus sought by the United States. The flowchart conclusively proves a secret federal plot to develop a "contagious cancer" that "selectively kills."
Following the presentation of the flowchart in Canada, the same information was presented to the United States in the rotunda of the Western Reserve Historical Society in Cleveland. Shortly thereafter a major African newspaper called and for four days in a row, this issue was the feature story in an uncensored press. The people of Africa already know about the U.S. virus development program. It is time for the rest of us to know.
In January, the U.S. had no response to my two page abstract submitted to the African American AIDS 2000 conference. In February, the U.S. Congress had no response to the 3000 Americans who signed signature petitions calling for immediate review of the flowchart and progress reports of the secret virus development program. We firmly believe once the dust settles from the current election marathon, reviewing the special virus program will be the single most important pursuit of the 21st Century.
More scientists and doctors must join with Dr. Nicolson, Dr. Strecker, Dr. Cantwell, Dr. Horowitz, Dr. Lee, Dr. Wainwright, Dr. Halstead and Professor Boyle. In any public debate on this issue, we will continue to present the flowchart of the secret virus development program, as the "irrefutable missing link" in the true laboratory origin of AIDS.
We have successfully navigated a federal maze and matrix and found a curtain surrounding the issue of AIDS. The 1999 discovery and presentation of the AIDS flowchart is a "smoke detector" wake up call. Society has an obligation to do more than don masks.
Non-inclusive random endnotes:
U.S. Special Virus program, Progress Report #8 (1971), pg. 61 (the flowchart)
National Security Defense Memorandum (NSDM) #314, Brent Scowcroft (1975).
"Special Message to the U.S. Congress on Problems of Population Growth", Richard M. Nixon, July 18, 1969
Public Law 91-213, "To Stabilize World Populations", John D. Rockefeller, III, Chairman, March 16, 1970
National Security Council Memorandum (NSCM) #46, "Black Africa and the U.S. Black Movement", Zbigniew Brezinski, March 17, 1978
AIDS is not the "worst" virus ever to arrive on this earth as the first poster states. AIDS is a very deadly virus but its method of transmission does not include either air-based (as in coughing or sneezing) or contagious from a touch. Whilst I never would describe AIDS as anything but serious, it is possible to avoid getting a blood/body fluids-bourne virus by becoming aware of how it is spread. Such a virus can be passed from one person to the next, such as in-vitro, without the contact being able to avoid it, but these cases are rare. Most of us can protect ourselves now from being infected by AIDS because we understand its method of transmission.
An example of a worse virus would be the air-bourne Bird Flu, which is transmitted by coughing and sneezing as well as all the other ways, and in the early 20th century as Spanish Fu the same or related virus caused more deaths in American troops than were killed by war in 1918, and also a world wide epidemic.
Elisa, I would say that as of this point the AIDS virus has killed the most people of any virus. Now, should the bird flu virus be released by the government on the people of the world as it appears they tried to do recently, then that would possibly eclipse the death count of AIDS, but so far, I do believe AIDS has killed more people. Is it as deadly as another? No, but then again, we don't have those running rampant right now, do we?
I can't locate the book this reference is in, but I read that also in the 70s, the WHO issued an internal document detailing the pressing need to investigate whether a virus could be constructed through genetic insertion or deletion that would disable human immune response. The book then goes on to quote an article from the Sydney Morning Herald newspaper in which a "mad scientist" claims that AIDS was "invented" by humans because AIDS was identical to an immune-suppressant sheep disease except for one genetic locus. The claim was that human agents had genetically manipulated the virus so that it was human specific. I'll find the book soon, and give you exact quotes and references.
The chart no longer seems downloadable via that link - a donation is required, but their account can no longer accept donations :).Quote:
Posted by Unified Serenity
Consider instead http://www.deepspace4.com/pages/dise...sflowchart.htm
Thank you Paul, that link works well. I took the liberty to copy part of the timeline given on that link and it is quite chilling. If one takes this information and watches MAAFA 21 it becomes apparent that there has been a definative Eugenics program to destroy the black race, and they are helping do it by supporting politicians who vote for such programs as this special virus program and planned parenthood assistance.
From the link:
Quote:
In 1961, scientist Haldor Thomar publishes that viruses cause cancer. In 1995, he and Carlton Gajdusek informed the National Academy of Sciences that “the study of visna in sheep would be the best test for candidate anti-HIV drugs.”
In 1962, under the cover of cancer research, the United States charts a path to commit premeditated murder, the “Special Virus” program begins on February 12th. Dr. Len Hayflick sets up a U.S. mycoplasma laboratory at Stanford University. Many believe the “Special Virus” program began in November 1961 with a Phizer contract.
Beginning in 1963 and for every year thereafter, the “Special Virus” program conducted annual progress reviews at Hershey Medical Center, Hershey, PA. The annual meetings are representative of the aggressive nature in which the United States pursued the development of AIDS.
In 1964, the United States Congress gave full support for the leukemia/lymphoma (AIDS) virus research.
In 1967, the National Academy of Sciences launched a full scale assault on Africa. The CIA (Technical Services Division) acknowledged its secret inoculator program.
In 1969, Fort Detrick told world scientists and the Pentagon asked for more money, they knew they could make AIDS. Nixon’s July 18 secret memo to Congress on “Overpopulation” serves as the start of the paper trail of the AIDS Holocaust.
In 1970, President Nixon signed PL91-213 and John D. Rockefeller, III became the “Population Czar.” Nixon’s August 10 National Security Memo leaves no doubt as to the genocidal nature of depopulation.
In 1971, Progress Report #8 is issued. The flowchart (pg. 61) will forever resolve the true laboratory birth origin of AIDS. Eventually the Special Virus program will issue 15 reports and over 20,000 scientific papers. The flowchart links every scientific paper, medical experiment and U.S. contract. The flowchart would remain “missing” until 1999. World scientists were stunned. The flowchart will gain in significance throughout the 21st Century. It is also clear the experiments conducted under Phase IV-A of the flowchart are our best route to better therapy and treatment for people living with HIV/AIDS. The first sixty pages of progress report #8 of the Special Virus program prove conclusively the specific goal of the program. By June 1977, the Special Virus program had produced 15, 000 gallons of AIDS. The AIDS virus was attached as complement to vaccines sent to Africa and Manhattan. However, because of the thoroughness of authors, like Dr. Robert E. Lee, we also learn the Stanford Mycoplasma Laboratory issues one of the first papers with AIDS in the title. “Viral Infections in Man Associated with Acquired Immunological Deficiency States.” The primary scientist, Dr. Thomas Merigan, was a “consultant” to the Special Virus program.
Progress Report # 8 at 104 - 106 proves Dr. Robert Gallo was secretly working on the development of AIDS with full support of the sector of the U.S. government that seeks to kill its citizens. Dr. Gallo can not explain why he excluded his role as a “project officer” for the Special Virus program from his biographical book. Dr. Gallo’s early work and discoveries will finally be viewed in relation to the flowchart. We now know where every experiment fits into the flowchart. The “research logic” is irrefutable evidence of a federal “Manhattan-style project” to develop a “contagious” cancer that “selectively” kills. Dr. Gallo’s 1971 paper is identical to his 1984 AIDS announcement.
Progress Report #8 at 273 - 286 proves we gave AIDS to monkeys. Since 1962, the United States and Dr. Robert Gallo have been inoculating monkeys and re-releasing them back into the wild. Thus, even government scientists are baffled that both HIV-1 and HIV-II would “suddenly emerge” from two distinct monkey ancestral relatives during the last 100 years. A 1999 Japanese study will ultimately prove the Man to Monkey origin of Monkey AIDS. The monkey experiments summary definitively proves Monkey AIDS is also man-made.
In 1972, the United States and the Soviet Union entered into a biological agreement that would signal the death knell for the Black Population. The 1972 agreement for collaboration and cooperation in the development of offensive biological agents is still U. S. policy.
In 1973, we find that world scientist, Garth Nicolson reports on his project, “Role of the Cell Surface in Escape From Immunological Surveillance.” His report is accompanied by seven published papers. Dr. Nicolson worked in conjunction with the Special Virus program from 1972 until 1978. Dr. Nicolson is considered by some to be Dr. Gallo’s “West Coast” counterpart. It is strongly held that because of Dr. Nicolson, Dr. Robert Gallo and Dr. Luc Montagnier would secretly meet in Southern California to coordinate what they would and would not say about the special virus development program.
In 1974, Furher Henry Kissinger releases his NSSM-200 (U.S. Plan to Address Overpopulation). It is the only issue of discussion at the World Population Conference in Bucharest, Romania. The men in the shadows had won, the whole world agrees to secretly cull Africa’s population. Today it is Africa and other undesirables. Tomorrow it may be you.
In 1975, President Gerald Ford signs National Security Defense Memorandum #314. The United States implements the Kissinger NSSM-200.
In 1976, the United States issues Progress Report #13 of the Special Virus program. The report proves the United States had various international agreements with the Russians, Germans, British, French, Canadians and Japanese. The plot to kill Black people has wide international support. In March, the Special Virus began production of the AIDS virus, by June 1977, the program will have produced 15,000 gallons of AIDS. President Jimmy Carter allows for the continuation of the secret plan to cull the Black Population.
In 1977, Dr. Robert Gallo and the top Soviet Scientists meet to discuss the proliferation of the 15,000 gallons of AIDS. They attach AIDS as complement to the Small pox vaccine for Africa, and the “experimental” hepatitis B vaccine for Manhattan. According to authors June Goodfield and Alan Cantwell, it is Batch #751 that was administered in New York to thousands of innocent people. This government will never be able to repay the people for the social rape, humiliation and out right prejudice people with HIV/AIDS face on a daily basis. The men in the shadows of the AIDS curtain accurately calculated that you would not care if only Blacks and gays are dying. In fact you don’t care that nearly a half million Gulf War veterans are encumbered with something contagious. Soon there will be no more Black people and a confused military, older White people will start suddenly dying and you still won’t get it. Be here now for us, give us a chance to be there for you.
Suddenly, just as President Nixon had predicted, there was explosive death. On November 4, 1999, the U.S. White House announced,.... “Within a period as short as five years, all new infections of HIV in the United States will be African American....” At some point our experts must be allowed to begin the interface process of allowing the history of this virus program to count. It is ludicrous and preposterous to fail to review the U.S. virus program in which to elucidate the etiology of AIDS.
More of the history of the secret virus program can be found in the archives of Dr. John B. Moloney. A review of the files under Dr. Moloney’s name would further pinpoint additional dates and records consistent with one of the greatest hunts, capture and proliferation of disease in the history of the human race. We have found the missing link. It is the guts of the research logic of a federal program that seeks to kill. We have found a curtain of AIDS. We can identify some of the people who work in the shadows of the curtain. Dr. Robert Gallo and Dr. Garth Nicolson must lead us in review. In light of the attack mechanisms available in which to inhibit AIDS, it is time that not another person be stricken with this relic, synthetic mycoplasma chimera.
Help those of us who are still here to realize full and contributory lives. We are all one people.
On September 28, 1998 I filed suit against the United States for the “creation”, “production” and “proliferation” of AIDS. On November 7, 2000, the appeals court agreed with the lower court and held AIDS bioengineering as “frivolous.” The world continues to wait for the court to rule on the resubmitted issues. The court can not continue to simply brush aside our experts and the government’s flowchart.
I have been asked to give my perspective with regard to the federal program MK-NAOMI . MK-NAOMI is the code for the development of AIDS. The “MK” portion stands for the two co-authors of the AIDS virus, Robert Manaker and Paul Kotin. The “NAOMI” portion stands for “Negroes are Only Momentary Individuals.” The U.S. government continues to orchestrate silence from the very top echelons of the Congress and military. At present there is no accountability. The good people will ultimately create a tsunami of public outrage. We can not allow the state an autocratic right to govern outside of the Constitution. Our society is structured to hide crimes committed by the state, while punishing citizens for minor indiscretions. Their strategy focuses on the general confusion they can create via manipulation of the media. They are very good at what they do. We must become more focused in our continued presentation of the flowchart. The flowchart is the absolute missing link in proving the existence of a coordinated research program to develop a cancer virus that depletes the immune system. New diseases do not create old illnesses.
This compilation of court documents and correspondence is the true effort of one man’s achievement in solving the mystery of the origin of AIDS. We have found the origin of AIDS, it is us.
THE SMOKING GUN OF AIDS: A 1971 FLOWCHART
In 1977, a secret federal virus program produced 15,000 gallons of AIDS. The record reveals the United States was represented by Dr. Robert Gallo and the USSR was represented by Dr. Novakhatskiy of the diabolical Ivanosky Institute. On August 21, 1999, the world first saw the flowchart of the plot to thin the Black Population.
The 1971 AIDS flowchart coordinates over 20,000 scientific papers and fifteen years of progress reports of a secret federal virus development program. The epidemiology of AIDS is an identical match to the "research logic" identified in the five section foldout. The flowchart is page 61 of Progress Report #8 (1971) of the Special Virus program of the United States of America. We today, challenge world scientists to discussion of this document find. We believe there is a daily, growing number of world experts who are all coming to the same conclusion regarding the significance of the flowchart. Dr. Garth Nicolson has examined the flowchart as well as other top notch experts from around the world. It is time for Dr. Michael Morrissey of Germany to examine the flowchart and report to the world. In addition, we have now examined the 1978 report. It is heresy to continue to further argue the program ended in 1977. The 1978 report of the development of AIDS leaves no doubt as to the ("narrow result") candidate virus sought by the United States. The flowchart conclusively proves a secret federal plot to develop a "contagious cancer" that "selectively kills."
Following the presentation of the flowchart in Canada, the same information was presented to the United States in the rotunda of the Western Reserve Historical Society in Cleveland. Shortly thereafter a major African newspaper called and for four days in a row, this issue was the feature story in an uncensored press. The people of Africa already know about the U.S. virus development program. It is time for the rest of us to know.
In January, the U.S. had no response to my two page abstract submitted to the African American AIDS 2000 conference. In February, the U.S. Congress had no response to the 3000 Americans who signed signature petitions calling for immediate review of the flowchart and progress reports of the secret virus development program. We firmly believe once the dust settles from the current election marathon, reviewing the special virus program will be the single most important pursuit of the 21st Century.
Cancer is a great business for oncologists. I am not saying every doctor who treats cancer patients is an evil SOB who knows there is a cure for cancer and that people are being purposefully damaged to later contract cancer. I am saying, what the hell is rat mitochondrial DNA doing in breast cancer patient tissue? Well, that is also part of the video presentation at 26:22. So far, I am having difficulty connecting the dots, but as I do not trust the AMA to do anything ethical, I think it's best to keep digging. Just remember everytime they want to give us another vaccine that there might be "other" things in it besides some killed virus.
Ok, I don't like wiki a lot due to it being easily manipulated, but I did find this:
http://en.wikipedia.org/wiki/Mouse_m..._breast_cancer
MMTV has been found in human breast cancer. A complete proviral sequence that was greater than 95% homologous to MMTV was sequenced out of human breast cancer tissue including a correct integration into the human genome. It was named Human Mammary Tumor Virus (HMTV). There has even been a correlation to an increased prevalence of HMTV with gestational breast cancer (62% for gestational BC (=gestational breast cancer) compared with 38% for all BC) indicating that the virus may retain its hormonal regulation.[5][citation needed] Early indications of MMTV (or MMTV like) virus involvement were confused by the presence of Human Endogenous RetroVirus (HERV) sequences that have a much lower level of homology to MMTV than HMTV. These were traces of one or more viruses similar to MMTV.[6][citation needed] It is emerging that many human breast cancers contain part of the env gene of a virus that is very close to MMTV. The presence of HMTV (not HERV) sequences has been found by multiple researchers in up to 42% of breast cancers in Europe, North America[7][citation needed] as well as Australia.[8][citation needed] This is compared to only 1 to 2% of the healthy population. While some consider the presence of MMTV in humans controversial, there is a large amount of evidence that MMTV (or a very close relative) plays a role in some human breast cancers.
In the last few years a number of labs have found MMTV like DNA in human breast cancer tissue and most recently, the virus has been shown to be able to productively infect human cells, possibly suggesting that an MMTV like virus may play a role in human breast cancer.
One theory of how MMTV would be passed to humans is through contact with our pets. Although it is difficult to imagine how modern women would get infected by a mouse virus, an infection of both species by the same food might be a possibility, or passage from one species to the other may also occur.[citation needed]This mode of infection might explain the often seen development of benign or malignant mammary tumors in pets.[citation needed]Dogs and cats are often affected and they too have access to human food and share living space with humans.
I have an idea. They are injecting women with this crap and people are dying.
What we are faced with is a systematic and multi-pronged attack on the integrity of the human genome, running concurrently with an attacking likewise on the human energetic field. There are documented studies of treatments for cancer that have been 8-balled, including amino acid therapy, and THC therapy. Both therapies delivered astounding results on patients whom the medical profession deemed as dead persons walking.Quote:
Posted by Unified Serenity
And on the human genome - what exactly was the "human genome project" about? The cost of it must have been enormous, and I would interested to know where the funding came from, or if it was "clean" money, where the impetus? The mapping of the human genome leads itself to abuse on many levels - what makes one ethnic group different from others? Can that difference be used to manufacture racially targeted lethal viruses? Where are the weak points in the human genome? How can animal viruses be targeted to humans? Which loci need changing? It's frightening stuff, but stuff we must face, harrowing though it may be to anyone with a heart.
I had read, a long time ago, that aids was created by the american government
to kill off all blacks in the world. The testing started in africa, but the virus
mutated and now it kills or tries to, any person of any race.
The plans still is to kill any person of any color but white.