The Plan – The Invisible Enemy – The Silent War – The Depopulation Agenda Moves Forward.

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The Silent War Continues.

(In his 2006 book, “State of Denial,” Bob Woodward wrote that Mr. Kissinger had “a powerful, largely invisible influence” on that administration’s foreign policy, and met regularly with Vice President Dick Cheney.)

The Depopulation Plan

United Nations Population Fund in 1970

As Jurriaan Maessen reports, the World Health Organization, one of GAVI’s partners, teamed up with the World Bank and UN Population Fund in the 1970’s under the “Task Force on Vaccines for Fertility Regulation”. The Task Force.

“…acts as a global coordinating body for anti-fertility vaccine R&D in the various working groups and supports research on different approaches, such as anti-sperm and anti-ovum vaccines and vaccines designed to neutralize the biological functions of hCG. The Task Force has succeeded in developing a prototype of an anti-hCG-vaccine.” pg. 3

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The Science of Fear:

THE KISSINGER REPORT 1974 (Depopulation)

Henry Kissinger – Secretary of State, National Security Advisor

The “primary aim” of the Plan of Action is asserted to be “to expand and deepen the capacities of countries to deal effectively with their national and subnational population problems and to promote an appropriate international response to their needs by increasing international activity in research, the exchange of information, and the provision of assistance on request (Pg.68).”

  • The following areas appear to contain significant promise in effecting fertility declines, and are discussed in subsequent sections: (Pgs. 79-80)
  • Providing minimal levels of education especially for women
  • Reducing infant and child mortality
  • Expanding opportunities for wage employment especially for women
  • Developing alternatives to “social security” support provided by children to aging parents.
  • Pursuing development strategies that skew income growth toward the poor, especially rural development focusing on rural poverty.
  • Concentrating on the education and indoctrination of the rising generation of children regarding the desirability of smaller family size.

The U.S. strengthened its credibility as an advocate of lower population growth rates by explaining that, while it did not have a single written action population policy, it did have legislation, Executive Branch policies and court decisions that amounted to a national policy and that our national fertility level was already below replacement and seemed likely to attain a stable population by 2000 (pg. 81).

In Section II Action to Create Conditions for Fertility Decline: Population and a Development Assistance Strategy, we see under B, “Functional Assistance Programs to Create Conditions for Fertility Decline.”

The U.S. also proposed to join with other developed countries in an international collaborative effort of research in human reproduction and fertility control covering big-medical and socio- economic factors.

Henry Kissinger referred to a commission report according to which population of 13 nations was to be slashed by starving them to death.

These countries are:






The Philippines








The U.S. further offered to collaborate with other interested donor countries and organizations (e.g., WHO, UNFPA, World Bank, UNICEF) to encourage further action by LDC (Less Developed Countries) governments and other institutions to provide low-cost, basic preventive health services, including maternal and child health and family planning services, reaching out into the remote rural areas.

Planned Parenthood in The U.S.

The U.S. delegation also said the U.S. would request from the Congress increased U.S. bilateral assistance to population-family planning programs, and additional amounts for essential functional activities and our contribution to the UNFPA if countries showed an interest in such assistance.

Each of these commitments is important and should be pursued by the U.S. Government.

Thus, the push for abortion, birth control, LGB Agenda, and breaking up the family.

The Rockefeller Foundation and Presidential Review 5 year report from 1968.

How to turn vaccines into killer diseases.

Bulletin: World Health Volume 47(2); 1972

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 Summary Page Browse PDF–1.2MCite
  2. 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 Summary Page Browse PDF–1.5MCite

The above information explains how to compromise an immune system by mixing animal cells with human cells. This process will also work using damaged aborted fetal tissue.

There is absolutely no need to use animal cells or aborted fetal tissue in a vaccine unless you are using the infected animal /human cells as a vector to poison the human host.

Prime example: SV 40 Virus caused Cancer.

In the late 1970s, it was predicted that gene therapy would be applied to humans within a decade. However, despite some success, gene therapy has still not become a routine practice in medicine. In this review, we will examine the problems, both experimental and clinical, associated with the use of viral material for transgenic insertion.

We shall also discuss the development of viral vectors involving the most important vector types derived from retroviruses, adenoviruses, herpes simplex viruses and adeno-associated viruses. This article is part of a themed section on Vector Design and Drug Delivery.

Being parasites, viruses have evolved to evade the immune system while at the same time the immune system has evolved to destroy viruses; hence, if viral vectors are destroyed or if the immune response recognizes and eliminates transduced cells, all potential benefit is lost (Nunes et al., 1999).

Viral Vector – mRNA gene therapies introduce toxins/poison into the body.

Opportunities and Challenges in the Delivery of mRNA-Based Vaccines.

Exosome-mediated delivery of gene vectors for gene therapy!divAbstract

Pathogenic priming likely contributes to serious and critical illness and mortality in COVID-19 via autoimmunity.

The relationship between the WHO and the Rockefeller Foundation is intense. In the 1986 bulletin of the World Health Organization, this relationship is being described in some detail.

While researching the effectiveness of “gossypol” as an “antifertility agent”, the bulletin states:

“The Rockefeller Foundation has supported limited clinical trials in China and small-scale clinical studies in Brazil and Austria. The dose administered in the current Chinese trial has been reduced from 20 mg to 10-15 mg/day during the loading phase in order to see if severe oligospermia rather than consistent azoospermia would be adequate for an acceptable, non-toxic and reversible effect. Meanwhile, both the WHO human reproduction programme and the Rockefeller Foundation are supporting animal studies to better define the mechanism of action of gossypol.

Fertility Regulating Vaccines

Soon after anti-fertility vaccines were successfully developed, hCG (Human chorionic gonadotrophin) containing Tetanus vaccines were deployed across multiple third-world countries. Many of these countries were specifically targeted in the U.S. Government’s 1974 National Security Memorandum 200 document for population reduction. The document recommended at the time in 1974 that “injectable contraceptives” receive further funding.

In August of 1992, a series of meetings was held in Geneva, Switzerland, regarding “fertility regulating vaccines”. According to the document Fertility Regulating Vaccines (classified by the WHO with a limited distribution) present at those meetings were scientists and clinicians from all over the globe, including then biomedical researcher of the American Agency for International development, and current research-chief of USAID, Mr. Jeff Spieler.

The Goal of Every H1N1 Swine Flu Vaccine: Immunotoxicity, Neurotoxicity and Sterility

Additional Links for vaccine information:

The Bill Gates “Plan”

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Moving along the timelines of population control, apparent eugenicist Bill Gates of Microsoft fame, brazenly set forth his ‘theorem’ for population control in a February 2010 TED speech he delivered.

Fauci and Birx have long track records of working with Bill Gates and his eugenicist vision for the world.

Fauci sits on the Leadership Council for the Global Vaccine Action Plan, a project of the Bill and Melinda Gates Foundation that works in concert with the United Nations. [See Gates’s press release on that project which documents Fauci’s role].

NEW YORK — The World Health Organization (WHO), UNICEF, the National Institute of Allergy and Infectious Diseases (NIAID) and the Bill & Melinda Gates Foundation have announced a collaboration to increase coordination across the international vaccine community and create a Global Vaccine Action Plan.  This plan will build on the successes of current work to achieve key milestones in the discovery, development and delivery of lifesaving vaccines to the most vulnerable populations in the poorest countries over the next decade.

The collaboration follows the January 2010 call by Bill and Melinda Gates for the next ten years to be the Decade of Vaccines.  The Global Vaccine Action Plan will enable greater coordination across all stakeholder groups – national governments, multilateral organizations, civil society, the private sector and philanthropic organizations — and will identify critical policy, resource, and other gaps that must be addressed to realize the life-saving potential of vaccines.

The United Nations Agenda 2030, adopted in 2015 and fiercely promoted and funded by the Gates Foundation, consists of 17 Sustainable Development Goals [aka Green New Deal] to be achieved by the year 2030.

Goal number 3, “good health and wellbeing,” begins with the U.N.’s demand that you “vaccinate your family.” 

Goal 3.8 states: “Achieve universal health coverage, including financial risk protection, access to quality essential healthcare services and access to safe, effective, quality and affordable essential medicines and vaccines for all.” [Emphasis added]

Goal number 16.9 says “By 2030, provide legal identity for all, including birth registration.”

The UN’s 2030 Agenda motto, repeated endlessly in its documents, is that this agenda will “leave no one behind.”

Gates has poured billions into furthering access to abortion. His vaccine projects have left thousands of women sterile in Kenya and India, and his polio vaccines have caused paralysis in Afghanistan, Congo and the Philippines. [For more on Gates’s horrific track record on vaccines, leaving a trail of death and serious injury, read Robert F. Kennedy Jr.’s scathing report, published by Children’s Health Defense on April 9, 2020 under the title Gates’ Globalist Vaccine Agenda: A Win-Win for Pharma and Mandatory Vaccination.]

Bill and Melinda Gates foundation are using their altruistic and laudable campaign to improve 3rd world healthcare to increase female infertility in the 3rd world. 

This global ID system is being designed as we speak by the New York City-based ID2020 Alliance.  Gates’s Microsoft Corp. became one of the founding partners in January 2018 along with Gavi Vaccine Alliance, another Gates-funded project. Funding also comes from longtime Gates collaborator the Rockefeller Foundation.

Bill Gates has now monopolized every area of United Nations for Global Domination:

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Links to many of Bill Gates Nefarious programs and products:


Bill Gates’ father, William Gates Sr., is co-chair of the Bill and Melinda Gates Foundation and a former board member for Planned Parenthood. Fauci and the Gates clan move in the same circles as the America-hating social engineering billionaire George Soros [see photo below from 2001].

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George Soros

Soros is a prolific financier of left-wing causes throughout the United States and around the world, including abortion, euthanasia, population control, same-sex “marriage,” transgenderism, and more.

His Open Society Foundations spend almost $1 billion annually in 100 different countries, including $150 million per year funding the left-wing American Civil Liberties Union (ACLU), the leading abortion company Planned Parenthood, and other liberal groups. He invested $5.1 million in a super PAC dedicated to funding groups working against Trump’s re-election; and is an aggressive supporter of the European Union who has spent money in hopes of influencing the elections of multiple European nations.

Rockefeller Foundation White Papers

Back in 2010, the Rockefeller Foundation put out a 54-page white paper titled “Scenarios for the Future of Technology and International Development.”

In this paper, the foundation gamed out a future pandemic based on a flu-like virus that attacks the human respiratory system.

National Covid-19 Testing Action Plan Pragmatic steps to reopen our workplaces and our communities April 21, 2020

The Roadmap for “The Depopulation Plan”


Military orders for aids-like viruses: The Biological Weapons Contractors

Horowitz, L. G. (1999). Emerging Viruses: Aids and Ebola. Rockport MA: Tetrahedron.


  • The year following the $10 million appropriation by the DOD for Aids-like biological weapons research, The NCI acquired the lion’s share of the facilities at America’s premier biological weapons testing center, Fort Detrick in Frederick, Maryland.


  • Robert Gallo is credited with modifying simian (i.e. monkey) viruses by infusing them with cat leukemia RNA to make them cause cancers as seen in AIDS patients.
  • Gallo’s discovery of adding a synthetic RNA and feline (i.e. cat) leukemia virus (FELV) “template” to “human type C” viruses (associated with cancers of the lymph nodes), the rate of DNA production (and subsequent provirus synthesis) increased as much as thirty times. The NCI researchers reported that such a virus may cause many cancers besides leukemias and lymphomas including sarcomas.


  • NCI reports revealed that Litton Bionetics had been granted the service contract to supply all NCI researchers, worldwide, with virtually every primate cancer research material requested, including seed viruses, viral hybrids, cell lines, experimental reagents, and African colony born monkeys including M. Mulatta and C. Aethiops which were associated with the major monkey AIDS virus outbreaks in California’s Davis Lab, and the 1967 Marburg virus outbreaks in three European vaccine production facilities.


  • After Nixon declared an end to the U.S. bio-weapons program, debate in the Army centered around whether toxin weapons were included in the president’s declaration. Following Nixon’s November 1969 order, scientists at Fort Detrick worked on one toxin, Staphylococcus enterotoxin type B (SEB), for several more months.
  • Nixon ended the debate when he added toxins to the bio- weapons ban in February 1970. The U.S. also ran a series of experiments with anthrax, code named Project Bacchus, Project Clear Vision and Project Jefferson in the late 1990s and early 2000s.
  • It is not well publicized or widely known that the Central Intelligence Agency (CIA) exercises oversight of infectious disease agencies including the National Institute for Allergies and Infectious Diseases (NIAID) and the Centers for Disease Control and Prevention (CDC), along with important investigations including the Pentagon’s investigation in into Gulf War Illnesses.
  • This is arguably done for “national security” concerns. Their official pronouncements, however, often include conflicting and controversial military and public health determinations.


  • Operation Trojan Horse
  • In 1977, The World Health Organization instigated a massive campaign in Africa to eradicate smallpox among the urban population. Over 100 million Africans were deliberately inoculated the AID-contaminated smallpox vaccine.
  • In 1978, over 2000 white male homosexuals were inoculated against hepatitis B by the Centers for Disease Control and the New York Blood Center, also with AIDS- contaminated vaccine.
  • Merck, Sharp, and Dohme (MSD) funded the hepatitis B vaccine research that Dr. Strecker claimed spread HIV to homosexuals in the United States.

SPECIAL VIRUS CANCER PROGRAM Safety-Review-SV40-Contamination-of-Polio-Vaccine-and-Cancer/SV40_SummaryFINAL.pdf

  • Monkeys infected with monkey viruses to produce oral polio vaccines were responsible for HIV and the AIDS epidemic. It was well known that the first polio vaccine produced in the 1950’s – the inactivated polio vaccine created by Jonas Salk – was made using rhesus monkeys that were infected with a monkey virus called simian virus 40 or SV40.
  • Some of the polio vaccine administered from 1955-1963 was contaminated with a virus, called simian virus 40 (SV40). The virus came from the monkey kidney cell cultures used to produce the vaccine. Most, but not all, of the contamination was in the inactivated polio vaccine (IPV). Once the contamination was recognized, steps were taken to eliminate it from future vaccines.
  • Researchers have long wondered about the effects of the contaminated vaccine on people who received it. Although SV40 has biological properties consistent with a cancer-causing virus, it has not been conclusively established whether it might have caused cancer in humans. Studies of groups of people who received polio vaccine during 1955-1963 provide evidence of no increased cancer risk.

However, because these epidemiologic studies are sufficiently flawed, the committee concluded in their report that the evidence was inadequate to conclude whether the contaminated polio vaccine caused cancer. Because of the lack in biological evidence to support the theory that SV40-contamination of polio vaccines could have contributed to human cancers, the committee recommended continued public health attention in the form of policy analysis, communication, and targeted biological research.

The Dire Consequences of GMO Foods

Food Sovereignty

The Reagan Administration accommodated Monsanto and other private companies who manufactured questionably safe food products designed for worldwide trade. Genetically modified (GMO) products with little or no testing were introduced in the United States Market.

Are GMO Foods, Vaccines, and Big Pharma Producing an Infertile Generation?

Glyphosate Unsafe on any plate Food Testing Report-2016.

Genetically Modified Foods on Human Health

Weather as a Force Multiplier: Owning the Weather in 2025


Department of Defense Appropriations for 1970   ing

Funding for Development of the AIDS Virus


  • There are two things about the biological agent field I would like to mention. One is the possibility of technological surprise. Molecular biology is a field that is advancing very rapidly, and eminent biologists believe that within a period of 5 to 10 years it would be possible to produce a synthetic biological agent, an agent that does not naturally exist and for which no natural immunity could have been acquired.
  • Within the next 5 to 10 years, it would probably be possible to make a new infective microorganism which could differ in certain important aspects from any known disease- causing organisms. Most important of these is that it might be refractory to the immunological and therapeutic processes upon which we depend to maintain our relative freedom from infectious disease.
  • A research program to explore the feasibility of this could be completed in approximately 5 years at a total cost of $10 million.
  • It would be very difficult to establish such a program. Molecular biology is a relatively new science. There are not many highly competent scientists in the field. Almost all are in university laboratories, and they are generally adequately supported from sources other than DOD. However, it was considered possible to initiate an adequate program through the National Academy of Sciences – National Research Council (NAS-NRC).
  • The matter was discussed with the NAS-NRC, and tentative plans were plans were made to initiate the program. However, decreasing funds in CB, growing criticism of the CB program, and our reluctance to involve the NAS-NRC in such a controversial endeavor have led us to postpone it for the past 2 years.

It is a highly controversial issue and there are many who believe such research should not be undertaken lest it led to yet another method of massive killing of large populations. On the other hand, without the sure scientific knowledge that such a weapon is possible, and an understanding of the ways it could be done, there is little that can be done to devise defensive measures. Should an enemy develop it, there is little doubt that this is an important area of potential military technological inferiority in which there is no adequate research program.


Probably the most dramatic of all statistics is the emerging fact that in the USA, Autism is now one in 36! And it affects males four times more frequently than females, which means those males will have neither the knowledge, ability nor desire to mate and to reproduce! Automatic depopulation control?

According to an Autism Action Network recent (February 2018) email

In November the federal National Center for Health Statistics released the preliminary results of a study that showed between 2014 and 2016 the number of 3 to 17-year old’s diagnosed with autism rose by 23%, yielding a new autism rate of 2.76%, or 1 in 36 children, and 3.63%, or 1 in 28 boys.

This catastrophic news was greeted with complete silence by the federal government, the major media, and the largest autism organizations. Neither Autism Speaks nor the Autism Society of America found the results worthy of a press release.

The CDC and FDA are notorious for their fraudulent research and reports, which they send out to the world and World Health Organization as “fact” but are nothing short of deceptive Big Pharma propaganda to implement the apparent Rockefeller-agenda’s/Big Pharma world population reduction efforts under way for many decades, but geared up legally at least in the USA, by the mandatory vaccine program, which Congress only compounded by the 1986 vaccine law, which needs to be rescinded immediately, if not sooner!

Then there’s the most prominent evidence to date of issues regarding population control, in my opinion: Children’s health status in the USA is at an all-time low and they are not expected to live as long as their parents, whereas mandatory vaccine compliance is near an all-time high per 2016 data for children aged 19 to 35 months:

Diphtheria, Tetanus, Pertussis (4+ doses DTP, DT, or DTaP): 84.6%

Polio (3+ doses): 93.7%

Measles, Mumps, Rubella (MMR) (1+ doses): 91.9%

Haemophilus influenzae type b (Hib) (primary series + booster dose): 82.7%

Hepatitis B (Hep B) (3+ doses): 92.6%

Chickenpox (Varicella) (1+ doses): 91.8%

Pneumococcal conjugate vaccine (PCV) (4+ doses): 84.1%

Combined 7-vaccine series: 72.2%


Patent for Creation of Influenza #US20170151324A1

The present invention relates, in general, to attenuated swine influenza viruses having an impaired ability to antagonize the cellular interferon (IFN) response, and the use of such attenuated viruses in vaccine and pharmaceutical formulations. In particular, the invention relates to attenuated swine influenza viruses having modifications to a swine

NS1 gene that diminish or eliminate the ability of the NS1 gene product to antagonize the cellular IFN response. These viruses replicate in vivo, but demonstrate decreased replication, virulence and increased attenuation, and therefore are well suited for use in live virus vaccines, and pharmaceutical formulations.


United States Patent (10) Patent No.: US 8,124,101 B2 Palese et al. (45) Date of Patent: Feb. 28, 2012

The present invention relates, in general, to attenuated Swine. influenza viruses having an impaired ability to antagonize the cellular interferon (IFN) response, and the use of such viruses in vaccine and pharmaceutical formulations. The invention relates to attenuated Swine influenza viruses having modifications to a Swine NS1 gene or eliminate the ability of the NS1 gene product the cellular response. These viruses replicate in vivo, but demonstrate decreased replication, virulence and increased attenuation, and therefore are well suited for use in live virus vaccines, and pharmaceutical formulations.


The above study completed in the fall of 2012 and published in the journal Environmental Health Perspectives found a link between high Fluoride levels found naturally in drinking water in China and elsewhere in the world, and lower IQs in children. The paper looked at the results of 27 different studies, 26 of which found a link between high-fluoride drinking water and lower IQ. The average IQ difference between high and low fluoride areas was 7 points, the study found.

The true history of the origin of AIDS can be traced throughout the 20th Century and back to 1878. On April 29 of that year the United States passed a “FEDERAL QUARANTINE ACT”. The United States began a significant effort to investigate “causes” of epidemic diseases. In 1887, the effort was enhanced with the mandate of the U.S. “LABORATORY OF HYGIENE”. This lab was run by Dr. Joseph J. Kinyoun, a deep rooted-racist, who served the eugenics movement with dedication. Two years later, 1889, we were able to identify “mycoplasmas”, a transmissible agent, that is now found at the heart of human diseases, including (AIDS) HIV.

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Chapter Excerpt from “State Origin: The Evidence of the Laboratory Birth of AIDS” by Boyd E. Graves, J.D.

  • In 1893, we strengthened the Federal Quarantine Act and suddenly there was an explosion of polio.
  • In 1898, we knew we could use mycoplasma to cause epidemics, because we were able to do so in cattle, and we saw it in tobacco plants.
  • In 1899, the U.S. Congress began investigating “leprosy in the United States”.
  • In 1902, We organized a “Station for Experimental Evolution” and we were able to identify diseases of an ethnic nature.
  • In 1904, we used mycoplasma to cause an epidemic in horses.
  • In 1910, we used mycoplasma to cause an epidemic in fowl/birds.
  • In 1917, we formed the “Federation of the American Society for Experimental Biology” (FASEB).
  • In 1918, the influenza virus killed millions of unsuspecting. It was a flu virus modified with a horse mycoplasma for which human primates had no “acquired immunity”.
  • In 1921, lead eugenics philosopher, Bertrand Russell, publicly supported the “necessity for “organized” plagues” against the Black population.
  • In 1931, we secretly tested African Americans and we tested AIDS in sheep.
  • In 1935, we learned we could crystallize the tobacco mycoplasma, and it would remain infectious.
  • In 1943, we officially began our bio-warfare program. Shortly thereafter, we were finding our way to New Guinea to study mycoplasma in humans.
  • In 1945, we witnessed the greatest influx of foreign scientists in history into the U.S. biological program. Operation Paperclip will live in infamy as one of the darkest programs of a twisted parallel government fixated on genocide.
  • In 1946, the United States Navy hired Dr. Earl Traub, a notorious racist biologist.

May 1946 appropriations hearing confirms the existence of a “secret” biological weapon.

  • In 1948, we know that the United States confirmed the endorsement of “devising a scheme” in which to address the issue of overpopulation in certain racial groups. State Department’s George McKennan’s memo will forever illuminate the eugenics mendacity necessary for genocide of millions of innocent people.
  • In 1949, Dr. Bjorn Sigurdsson isolates the VISNA virus. Visna is man-made and shares some “unique DNA” with HIV. See, Proceedings of the United States, NAS, Vol. 92, pp. 3283 – 7, (April 11, 1995).
  • In 1951, we now know our government conducted its first virus attack on African Americans. Crates in Pennsylvania were tainted to see how many Negro crate handlers in Virginia would acquire the placebo virus… They were also experimentally infecting sheep and goats. According to author Eva Snead, they also held their first world conference on an AIDS-like virus.
  • In 1954, Dr. Bjorn Sigurdsson publishes his first paper on Visna virus and establishes himself as the “Grandfather of the AIDS virus.” He will encounter competition from Dr. Carlton Gajdusek.
  • In 1955, they were able to artificially assemble the tobacco mosaic virus. Mycoplasmas will forever be at the heart of the U.S. biological warfare program
  • In 1957, future U.S. president, Rep Gerald Ford and others gave the U.S. Pentagon permission to aggressively deploy offensive biological agents. There are no recorded cases of AIDS prior to the 1957 creation of “Special Operation-X.” (The SOX) program served as the immediate prototype program for the Special Virus program to begin in 1962.
  • By 1960, Nikita Kruschev had been let in on the biological weapon. His 1960 statement will long reflect the arrogance of the secret blend of communism and democracy. The two countries would go to a November 1972 agreement to cull the Black Population.
  • 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 Pfizer 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 clearly displays in a logical order of progression all of the experiments that resulted in this horrific immune deficiency. 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.” 0182.pdf
  • 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 at Fort Detrick with full support of the sector of the U.S. government that seeks to kill its citizens. Dr. Gallo cannot 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 fit 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, 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, 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. Yesterday it was Africa and other what was considered undesirables. Today it is us.
  • 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 Smallpox 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 daily. 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, no one seems to care that nearly 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 no one will still get it.
  • 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 humans. This timeline is the missing link. It is the guts of the research logic of a federal program that seeks to kill. Some of the people who work behind the curtain to cure Aids are Dr. Robert Gallo and Dr. Garth Nicolson. Considering the attack mechanisms that are now known and available in which to inhibit AIDS, not another person need be stricken with this relic, synthetic mycoplasma chimera.
  • Regarding 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 cannot continue to allow this atrocity to continue any longer.

We have found the origin of AIDS; it is us.

Experimenting with the GOD Gene:

The Gene Drive Dilemma: We Can Alter Entire Species, but Should We?

The Globalist strategy focuses on chaos, disinformation, division, total control and manipulation of the media. They are very good at what they do.

Our society has been programmed to ignore crimes committed by the government, while punishing citizens for minor indiscretions.

Legalized Propaganda . . . 2012 Smith-Mundt Act.

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Say NO to H.R. 6666 Tracing Act

Is Big Pharma behind suppressing treatments? Yes

Hydroxychloroquine + Zinc + Antibiotic treatment for Coronavirus Disease – CoVid

Treatments that are being hidden

We have many Covid-19 treatments that have been proven effective “We Do Not Need Any Vaccine”

The number of people suffering serious adverse events following vaccination from the Wuhan coronavirus (COVID-19) is 50 times higher than the number for seasonal flu shots, new reports indicate.

Please use Duck- Duck Go or The links will not work in a Google Search.

For more information on AIDS & its cure, visit and

For more Information on these critical topics, there are also many FREE videos online:

  • Google video search for ‘AIDS CURE: U.S. Patent #5676977

A method of treating AIDS-afflicted humans comprising injecting a multitude of tetra-silver tetroxide molecular crystals into the bloodstream of the human subject.

A method for increasing white blood cell counts in AIDS-afflicted humans comprising injecting a multitude of tetra-silver tetroxide molecular crystals into the bloodstream of the human subject.

Methods of treating AIDS-afflicted 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.

Interferon alpha

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Peptide T has several positive effects related to HIV disease and Neuro-AIDS

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Suramin, a 100-year-old drug that can help autistic kids

Just a single dose of drug called suramin can help children with autism spectrum disorder, says a new study.

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The Invisible enemy has been revealed. Their plan details mandatory vaccination for everyone and we cannot allow this insanity to continue any longer. We are literally in a fight for our minds and life. We cannot lose!

Know your rights:

Exposing Vaccine Genocide:

Saying No to Vaccines:

Deprivation of Rights Under Color of Law:

1 comments on “The Plan – The Invisible Enemy – The Silent War – The Depopulation Agenda Moves Forward.”

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