In an increasingly baby-minded world, I had to pull out the crayons again.
I feel embarrassed for the human race that I have to explain this and so many people need to see it.

These guys are funded by Bill Gates btw

Is It ‘Eugenics’ to Abort Unborn Babies with Down Syndrome?

By Alexandra DeSanctis, staff writer for National Review and a visiting fellow at the Ethics and Public Policy Center.

“On the legal blog Dorf on Lawin an article by Sherry F. Colb, a Cornell University law professor. Colb argues that, because eugenics is defined as “a movement . . . aimed at improving the genetic composition of the human race,” it is inapt to call selective abortions “eugenic,” because a woman who chooses abortion after a Down-syndrome diagnosis “understands that she is thereby doing virtually nothing to alter the human genome.”

But Colb ignores another meaning of the adjective “eugenic”: “relating to or fitted for the production of good offspring.” Though the term “eugenics” undoubtedly evokes a program of controlled, selective breeding to reshape a population, it is entirely accurate to describe as “eugenic” an individual choice to eliminate a child deemed “unfit,” even in just one instance.

Colb concludes with this argument:

What if everyone pregnant with a DS fetus terminates? What then? Do we want to live in a world in which DS people are extinct? No. There is no question but that people with DS, like people with all sorts of other challenges, enrich our world and teach us to tolerate those who differ from ourselves. It would indeed be sad if the world contained no one with DS. But just because we want a group of people in the world does not entitle us to conscript individuals to create such people in their wombs.

But of course, forbidding abortions chosen on the basis of disability cannot rightly be described as “conscripting individuals to create such people in their wombs.” When a pregnant mother receives a prenatal Down-syndrome diagnosis, she has already created a human being who might have Down syndrome (though such tests have been known to be wrong). Forbidding a woman from actively killing her unborn child based on its disability is not the same thing as conscripting her into creating that child.

That defenders of legal abortion are reduced to such arguments is telling. In the end, it doesn’t matter much whether we can rightly label certain abortions “eugenic” or whether one side of the debate has the most accurate history of racial discrimination and population control.

What matters is that, in Ohio, lawmakers have laid down a marker establishing that it is wrong and therefore that it is now illegal to end the life of an unborn human being simply because he or she is diagnosed with a chromosomal abnormality. Supporters of abortion refuse to respond to this argument, because to do so would expose the logic of all abortion, which, regardless of disabilities, grants some human beings the power to declare the lives of others not worth living.”

Gates conducted an interview with Bill Moyers on PBS to explain the rational for his charitable contributions:

MOYERS: You could have chosen any field, any subject, any issue and poured billions into it and been celebrated. How did you come to this one? To global health?

GATES: The one issue that really grabbed me as urgent were issues related to population… reproductive health.

And maybe the most interesting thing I learned is this thing that’s still surprising when I tell other people which is that, as you improve health in a society, population growth goes down.

You know I thought it was…before I learned about it, I thought it was paradoxical. Well if you improve health, aren’t you just dooming people to deal with such a lack of resources where they won’t be educated or they won’t have enough food? You know, sort of a Malthusian view of what would take place.

And the fact that health leads parents to decide, “okay, we don’t need to have as many children because the chance of having the less children being able to survive to be adults and take care of us, means we don’t have to have 7 or 8 children.” Now that was amazing.

So Gates is interested in improving health because he believes that would reduce the amount of people on the planet.  His goal is not to help people but to eliminate them.  He states that if people are healthy that they will want fewer kids but he doesn’t offer evidence to support this and frankly it doesn’t appear to make much sense. Why would a sick person who could die at anytime want to have kids if they knew there was a good possibility they wouldn’t be around to support the child?   Does Gates really believe this or is this just his cover story so not arouse any suspicions about his true motivations?  Gates also admits that he notes that he previously shared the opinion with Malthus that health should not be improved because that would encourage population growth.  If you remember Malthus wanted villages built near sewage to encourage disease.  Now he doesn’t disagree with Malthus that population growth is bad he only disagrees on how to reduce population.

I don’t believe that Gates’ actually thinks that improving health reduces population.  I think that he is using global health as a stalking horse to eliminate population.  Gates’ could donate money to provide basic healthcare to poor Africans like Doctors Without Borders, he could build hospitals, and he could help provide low cost health insurance to the millions who can’t afford it.  Bill Gates money could be spent improving access to safe drinking water and providing sanitation services.  His money is spent on any of this noble The elites of the world choose to spend the tax dollars of the American middle class on contraceptives, abortions, and vaccines.  Kenyan gynecologist Dr. Stephen Karanja observed, “USAID and other Non-Governmental organizations funded mainly by the U.S. Government have targeted our people with a ruthlessness that makes one shudder. Our health sector has collapsed. Thousands of the Kenyan people will die of malaria, whose treatment costs a few cents, in health facilities whose shelves are stocked to the roof with millions of dollars worth of pills, IUDs, Norplant, Depo-Provera, most of which are supplied with American money.”

“Many are maimed for life. The hypertension, blood clots, heart failure, liver pathology and menstrual disorders cannot be treated due to the poor health services…. Malaria is epidemic in Kenya. Mothers die from this disease every day because there is no chloroquine, when instead we have huge stockpiles of contraceptives.” – SOURCE – I used this not for authoritativeness, but for logic and because it very much speaks my mind too. And I fact-checked it.

IT WORKS BOTH WAYS, AS YOU BALANCE AND STEER IT.
SOURCE

THE AFRICAN PERSPECTIVE ON IT

Population Control is GENOCIDE

(This interview with Sister Aset was first published in Global Africa Pocket News (GAP News) Vol. 1, No. 7 Sept. 1994. It was submitted to Caribbean Times in January ’96 but never published) #14
SOURCE

What is population control?


The United Nations Population Fund would like us to believe that it is a benign process of ‘voluntary’ application of ‘family planning’ to control the ‘rate of growth’ of the world’s ‘sustainable’ population within ‘manageable’ levels in relation to the amount of ‘food’ and ‘consumable goods’ the earth can produce. That is as far from the truth as the divide between the very richest and the very poorest people on this planet.
The truth is that population control is the process by which Global Europe (whites, Caucasians, Aryans) seeks to guarantee its perpetual domination of the rest of the human race because of its own fear of annihilation. According to Dr. Frances Cress-Welsing, it is this fear based on the fact of their numerical minority status and their low level of surface melanin, which drives them to commit the most atrocious crimes against humanity, in particular, the most feared nation of all, Global Africa (Black people).


Is it true that the world is over crowded and moving towards an unsustainable population level?


No. Absolutely not. Overcrowding can be measured by one method only that is whether there are too many people to fit in the space available. The most densely populated continent area in the world is Europe, (see GAP News #7, Population Figures), but do Europeans think there are too many people in Europe? Of course not. But they believe there are too many African and Asian people in Europe. That is not overcrowding that is racism.


What about all those starving Africans? If they can’t feed themselves surely, there must be too many of them.


No, that is not the case. Those “starving Africans”, Asians and other “Third World” peoples produce most of the world’s surplus food. Most of the food they produce are luxury or raw, unprocessed goods which are sold cheaply as exports and re-imported as expensive processed foods.
The main reason though, why there appears to be not enough food to go around is not because the so-called third world cannot feed itself, it is because Global Europe, less than 25% of the world’s population uses or wastes over 80% of the worlds food goods (consumables) but produces less than 15% of it. So the “third world” make up 75% of the world’s population, produce 85% of the world’s consumables and consume less than 20% of all that is consumed. If they consumed as much as they produced, Global Europe would be dying of starvation, not Africa.


Is the African population expanding too rapidly?


Let’s look at the evidence: After being systematically depopulated for 400 years, Africa is now the least populated continent in the world with a density one-sixth of Europe’s. Africa’s death rate is more than twice that of Europe. To be level pegging, Africa’s death rate should also be one-sixth of Europe’s. When these dishonest people talk about population they make reference only to birth rate. They show that Africa’s birth rate is nearly three times that of the European rate, but forget to mention that the infant mortality rate is 5 times higher in Africa.
They never talk about density except in reference to Asia or to say that “Rwanda is the most densely populated country in Africa”. They forget to say it was a quarter the density of any country in Europe. They forget also, to tell you that in order for Africa to get to the same population density as Europe (is Europe overpopulated?) the African birth-rate has to be more than 12 times that of Europe (6 times if the death rate becomes equal) for a whole generation.
So, when they talk about “equalizing” or reducing the African birth rate, while at the same time nurturing conflict, manufacturing famine, and importing disease to increase the death rate further, you begin to get the picture. If the birth rates were made equal and everything else remained the same as they are now, each time Europe’s population doubled Africa’s population would be halved. The world’s population may become “stabilized” as they like to say it, but the percentage ratio between the nations would continue changing to their advantage. (See GAP News #5)
It is understandable then, why Cardinal Alfonso Lopez Trujillo, a senior Vatican official cried that if the precepts of the UN Population Control Conference in Cairo were to be implemented the world would experience “the most disastrous massacre in history”. He should know, it was his organization, the Roman Catholic church, which sanctified the trade in African lives, resulting in the death of over 200 million people.
Some of the liars say that deaths in war time make very little difference to the population growth because after a war birth rates usually increase to compensate. Certainly, that is true when mostly male soldiers are killed. But when two thirds of the female population are murdered, like the Rwandan slaughter, it would take 4 or 5 generations to get back to where it was before the war. And that is the key. The women.
Global Europe have done everything they could to destroy our people but we are still here and still strong. They are now trying, through an apparently limitless line of African and Asian female mercenaries, posing as leaders, to co-opt us. To convince us that regardless of our particular environmental conditions, contrary to our own community’s social and economic needs, it would be in our individual interests to have fewer or no children at all.
Women have the power to determine the fertility or sterility of our nation. It is imperative that we do not allow ourselves to be misled into committing generational suicide. We carry the future of our nation in our hands. We are here because those before us gave us life. Let us give life to our children. We deserve to live.

SOURCE

FRAGMENT:

ABORTION FOR EUGENICS: CONSPIRACY OR SIMPLE CONSEQUENCE?

How one answers the question whether abortion is a tool of racial, gender, or disability eugenics depends very much on how the question is asked. Is legalized abortion a eugenicist conspiracy — a deliberate plot on the part of those favoring abortion rights to reduce the number of people of a given race, sex, or disability? Surely not. At the very least, such motivations form no part of the modern argument for abortion rights. Does unrestricted legal abortion-choice produce a disparate impact resulting in disproportionate numbers of abortions ending the lives of minority, female, and disabled fetuses? Undeniably. The aborted are disproportionately Black, female, and disabled. Is the right to abortion sometimes used, by those exercising the abortion-choice, for eugenics purposes — specifically for the purpose of aborting on the basis of race, sex, or disability? Unquestionably. Some — but not all — of the abortion–disparate impact is attributable to intentional decisions to abort based on a trait of the baby that otherwise would be born.

These are three different questions. Justice Thomas’s concurrence in Box keeps them distinct. Murray’s article, in attempting to critique Thomas, tends to smush these separate questions together in a mildly confusing way.

Begin with Justice Thomas’s Box concurrence itself. Thomas’s opinion compiles an impressive and rightly disturbing narrative of evidence that family planning and abortion advocates in the past embraced the desirability of abortion as an instrument for achieving racial eugenics and for culling persons with disabilities from the population. (There appears to be no evidence that early abortion advocates ever favored abortion for gender-eugenics purposes — aborting girls because they are girls.18×18. This is probably most simply explained by the fact that the technology for discerning the fetus’s sex before birth was not readily available until relatively recently. See, e.g., Juan Stocker & Lorraine Evens, Fetal Sex Determination by Ultrasound, 50 OBSTETRICS & GYNECOLOGY 462, 465 (1977).

Han Chinese academics in Xinjiang in recent years have blamed the high birth rate among the Uyghurs and Kazaks for fostering religious extremism and poverty. According to Zenz’s research, government and academic papers have referred to the birth rate of ethnic minorities in the region as “excessive” and have claimed that the population growth and concentration of ethnic minorities in Xinjiang “weakens national identity and identification with the Chinese Nation-Race (Zhonghua Minzu).”

Population Research Institute

I’ve been meaning to put this together for this a long time now, but we owe it to An0maly that I arrived to finish it, he tipped me over with this great brand new video, where he kills it in his own terms. I just felt I need to round it up and bring more depth and definition that he can’t possibly achieve in his format. The guy is one of the clearest minds on Internet right now.

MORE References

To be continued?
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ORDER

THERE’S NO BETTER PREVENTION THAN SHARING THE KNOWLEDGE FASTER THAN THEY SHARE THEIR PROPAGANDA!

The original title of this article was URGENT! DEBUNKING THE NEXT ENGINEERED PANDEMIC: NIPAH VIRUS. I expanded the scope because in the meantime I learned they are ramping up propaganda for all three. These viruses have more things in common, as you will find out below.

UPDATE 6: NOVEMBER 9, 2021:

To further develop the ChAd3 Ebola and Marburg vaccines, Sabin has entered into a Research Collaboration Agreement with the Vaccine Research Center at the National Institute of Allergy and Infectious Diseases.
The Sabin Vaccine Institute, a non-profit organization founded in 1993, is a leading advocate for expanding vaccine access and uptake globally, advancing vaccine research and development, and amplifying vaccine knowledge and innovation. Sabin received more than $110 million for vaccine R&D programs from public and philanthropic funding sources, including the Bill & Melinda Gates Foundation, European Commission, Dutch Ministry of Foreign Affairs, Global Health Innovative Technology Fund and the Michelson Medical Research Foundation.

SABIN VACCINE INSTITUTE, August 6, 2019

Washington DC, Oct. 21, 2021 (GLOBE NEWSWIRE) — The Sabin Vaccine Institute (Sabin) announced that the Biomedical Advanced Research and Development Authority (BARDA), part of the Office of the Assistant Secretary for Preparedness and Response within the U.S. Department of Health and Human Services, has exercised the third contract option, valued at $34.5 million, under the 2019 contract to advance the development of vaccines against Ebola Sudan and Marburg viruses through Phase 2 clinical trials.  

In September 2019, BARDA awarded Sabin a development contract, valued up to $128 million, and has already provided funding of $40.5 million. This third contract option will enable continued nonclinical efficacy and safety studies, Phase 2 clinical trials in Africa, and vaccine manufacturing processes to ensure quality and safety.

In August, a case of Marburg disease was confirmed in the West African country of Guinea where the Ministry of Health officially declared an outbreak of Marburg.1 This recent case, as well as Marburg’s history of outbreaks and their potential for future devastating outbreaks, demonstrates that preventative measures are overdue to protect civilian populations, military personnel, first responders, health care workers and laboratory workers, both in the United States and abroad, against these emerging infectious diseases.

Ebola Sudan and Marburg viruses are closely related to Ebola Zaire virus, which has caused more than 2,200 deaths since 2018, leading the World Health Organization (WHO) to declare it a Public Health Emergency of International Concern. Like Ebola Zaire, Ebola Sudan and Marburg are among the world’s deadliest viruses, causing hemorrhagic fever with subsequent death in an average of 50 percent of cases.2,3

“Even as the world struggles with the COVID-19 pandemic, disease caused by Ebola Sudan and Marburg viruses continue to be a serious threat, as we have seen with the recent outbreak of Marburg in Guinea. We are grateful for BARDA’s continued support of Sabin’s efforts to advance vaccines against these deadly viruses,” said Sabin Chief Executive Officer Amy Finan. “We also thank our partners at the Vaccine Research Center of the NIH National Institute of Allergy and Infectious Diseases for their continued collaboration, and GSK for their earlier work on the candidates.” 

The two candidate vaccines, based on GSK’s proprietary ChAd3 platform, were exclusively licensed to the Sabin Vaccine Institute from GSK in 2019.

This project has been funded in whole or in part with federal funds from the U.S. Department of Health and Human Services; Office of the Assistant Secretary for Preparedness and Response; Biomedical Advanced Research and Development Authority, under contract number 75A50119C00055.

Learn more about Sabin’s Ebola Sudan and Marburg program.

This above is the official Sabin Inst. press release, this below isn’t:

November 4, 2021 – The U.S. CDC published a Level Three Travel Advisory for the recent Ebola outbreak in the Beni Health Zone of the Democratic Republic of the Congo.

November 3, 2021 – The U.S. CDC vaccine advisory committee reviewed previous recommendation preexposure vaccination with Ervebo for adults aged ≥18 years in the U.S. population who are at highest risk for potential occupational exposure to Ebola virus species Zaire ebolavirus because they are: responding to an outbreak of Ebola Virus Disease (EVD), or work as health care personnel at federally designated Ebola treatment centers in the U.S., or work as laboratorians or other staff at biosafety level 4 facilities in the U.S.

November 2, 2021 – The WHO reported additional cases and deaths confirmed in the Ebola virus disease outbreak in the Democratic Republic of the Congo with two new health areas affected. A total of 394 people (67 primary care providers including nine high-risk contacts, nine contacts of contacts, and 49 probable contacts) have been vaccinated including 182 contacts of contacts, 125 probable contacts, and 87 high-risk contacts.

October 29, 2021 – A Research Article – Safety and immunogenicity of 2-dose heterologous Ad26.ZEBOV, MVA-BN-Filo Ebola vaccination in healthy and HIV-infected adults: A randomized, placebo-controlled Phase II clinical trial in Africa – was published by the journal PLOS Medicine. Conclusion – The Ad26.ZEBOV and MVA-BN-Filo combo vaccination were well tolerated and immunogenic in healthy and HIV-infected African adults. Increasing the interval between vaccinations from 28 to 56 days improved the magnitude of humoral immune responses. Antibody levels persisted to at least 1 year, and an Ad26.ZEBOV booster vaccination demonstrated the presence of vaccination-induced immune memory. These data supported the approval by the European Union for prophylaxis against EBOV disease in adults and children ≥1 year of age.

October 27, 2021 – IAVI announced an award of up to US$126 million from the Biomedical Advanced Research and Development Authority to develop two recombinant vesicular stomatitis virus (rVSV)-vectored filovirus vaccine candidates. This award supports preclinical activities and includes options for clinical development up to and inclusive of a Phase II clinical trial of IAVI’s rVSV Sudan ebolavirus vaccine candidate (rVSVΔG-SUDV-GP). Optional work that would continue the development of IAVI’s Marburg virus vaccine candidate (rVSVΔG-MARV-GP) that is currently supported by the Defense Threat Reduction Agency of the U.S. Department of Defense could be funded at a later date.

“Vectored” means, most likely, mRNA or some other genetic / nanotech targeting technology.

October 20, 2021 – The WHO African Region reported 5 Ebola cases, and over 27,000 travelers have been screened in the DRC. Furthermore, over 116 people have been vaccinated.

October 17, 2021 – Africa News reported Ebola vaccinations started in Beni, DRC, after at least two people died due to the virus in October 2021. The WHO African Region Tweeted DRC Situation Report (17/10/21) 5 confirmed cases, three deaths, 369 contacts identified, and 308 contacts monitored.

October 13, 2021 – Democratic Republic of the Congo (DRC) health officials confirmed an Ebola vaccination campaign had launched in the North Kivu province where one confirmed Ebola case, plus three related suspected deaths, were recently reported. About 1,000 doses of the rVSV-ZEBOV Ebola vaccine and other medical supplies were delivered from the capital Kinshasa to Goma city in North Kivu. The DRC has more than 12,000 vaccine doses in Kinshasa that can be deployed if necessary.

October 10, 2021 – The WHO reported additional Ebola cases related to the recent DRC case of a 3-year-old boy. A cluster of three deaths (two children and their father) who were neighbors of the case. These three patients died on 14, 19, and 29 September 2021 after developing symptoms consistent with Ebola. However, none were tested for the virus. As of October 9th, a total of 148 contacts have been identified and are under follow-up by the local response team.

October 8, 2021 – A case of Ebola has been confirmed in the eastern Democratic Republic of the Congo, five months after the end of the most recent Ebola outbreak there. The child died on October 6th. It was not immediately known if the Ebola case was related to the 2018-20 outbreak that killed more than 2,200 people in eastern Congo or the flare-up that killed six people in 2021.

September 13, 2021 – A new study based in Sierra Leone concluded the Ebola vaccine regimen from Janssen – J&J. It was found well tolerated with no safety concerns in children aged 1–17 years and induced robust humoral immune responses, suggesting the suitability of this regimen for Ebola virus disease prevention in children.

August 31, 2021 – The government of Cote d’Ivoire has informed the WHO that a second laboratory has tested samples from a patient suspected of having Ebola and has found no evidence of the virus. Around a dozen WHO experts were mobilized to support the country’s efforts, and 5,000 Ebola vaccine doses which WHO had helped Guinea procure were sent from Guinea to Cote d’Ivoire.

August 23, 2021 – The WHO African region reported Ebola booster dose vaccinations in Sierra Leone following administration of the prime dose of the Johnson & Johnson Ebola vaccine in May 2021. Frontline health workers, practitioners of traditional medicines or traditional healers, and commercial motorbike riders who received the first dose are now given their second jab to maximize their protection against the disease. 

August 17, 2021 – The WHO confirmed Cote d’Ivoire deployed 2,000 vaccine doses from Merck and around 3,000 vaccine doses manufactured by Johnson & Johnson – Janssen.

August 14, 2021 – The WHO Africa reported the Ministry of Health of Cote d’Ivoire today confirmed the country’s first case of Ebola since 1994. This came after the Institut Pasteur in Cote d’Ivoire confirmed the Ebola Virus Disease in samples collected from a patient hospitalized in Abidjan’s commercial capital after arriving from Guinea.

August 9, 2021 – The WHO confirmed ‘Marburg virus disease (MVD) is a highly virulent, epidemic-prone disease associated with high case fatality rates (CFR 24-90%). In the early course of the disease, the clinical diagnosis of MVD is difficult to distinguish from other tropical febrile illnesses because of the similarities in the clinical symptoms. Differential diagnoses to be excluded include Ebola virus disease, as well as malaria, typhoid fever, leptospirosis, rickettsial infection, and plague.’

June 15, 2021 – The Southwest National Primate Research Center at Texas Biomedical Research Institute (Texas Biomed) has been awarded more than $37 million from the U.S. National Institutes of Health to continue operations into 2026. The P51 grant, given by the NIH Office of Research Infrastructure Programs, provides essential funding to house and care for nearly 2,500 non-human primates that are part of life-science research programs at Texas Biomed and partners around the globe.

June 4, 2021 – Johnson & Johnson welcomed a new recommendation by the Strategic Advisory Group of Experts on Immunization for the WHO that supports the use of the Johnson & Johnson Ebola vaccine regimen both during outbreaks for individuals at some risk of Ebola exposure and preventively, in the absence of an outbreak, for national and international first responders in neighboring areas or countries where an outbreak might spread.

June 4, 2021 – J&J confirmed about 235,000 people had received at least the first dose of the Janssen two-dose Ebola vaccine regimen.

April 10, 2021 – The government of Sierra Leone and the WHO announced Johnson & Johnson had donated about 4,500 Zabdeno and Mvabea Ebola vaccines to Sierra Leone to help prevent any Ebola outbreak. The last Ebola outbreak in Sierra Leone was in 2016.

March 25, 2021 – Ohio Gov. Mike DeWine revealed health officials are monitoring 44 people who have returned from areas of Africa with active outbreaks of Ebola.

March 25, 2021 – Oregon public health officials announced they are monitoring four people who recently visited the West African countries of Guinea and the Democratic Republic of the Congo. Regions in each of these countries are currently experiencing outbreaks of Ebola virus disease. The Oregon Health Authority and local public health departments have been in contact with these individuals, considered “persons under monitoring” since they arrived in the state earlier in March 2021.

March 23, 2021 – The WHO African Region Tweeted Guinea Ebola outbreak Situation Report (22/03/21) 18 cases, nine deaths, 78 contacts, 82% monitored. And 3,905 people have been vaccinated.

March 13, 2021 – After a request from the Guinean authorities, Russia is considering supplying a domestic vaccine against the Ebola virus to the African country, reported TASS.

May 13, 2020 – BARDA Provides the Sabin Vaccine Institute with an Additional $20 Million for Further Development of Ebola Sudan and Marburg Vaccines

The Sabin Vaccine Institute (Sabin) and its partner ReiThera Srl today announced that the Biomedical Advanced Research and Development Authority (BARDA), part of the Office of the Assistant Secretary for Preparedness and Response within the U.S. Department of Health and Human Services, has exercised the first two options, valued at $20 million, under the 2019 contract to advance the development of vaccines against Ebola Sudan and Marburg viruses through Phase 2 clinical trials. In September 2019, BARDA awarded Sabin a development contract, valued at $128 million, and provided the initial funding award of $20.5 million. This second $20 million award will enable the manufacture and release of clinical vaccine material developed by ReiThera, a specialist in the development and cGMP manufacture of adenoviral vector vaccines. The funding will also support non-clinical studies to evaluate efficacy and immune response.

UPDATE 5: NOVEMBER 7, 2021: MARBURG GOES VIRAL ON INTERNET ONLY, YET. I’m happy awareness increases, it’s crucial. I’ve addressed this virus below, but not many had the patience to go through all text, and I kind of understand them, but there’s no easier way than reading.
Here’s another angle to keep in sight when computing all this info:

UPDATE 4: OCTOBER 19 2021: THE FEARPORN CAMPAIGN TAKES SPEED AS IF THEY ARE TO RELEASE THIS SOON. IF YOU FALL FOR THEIR BRAINWASH, THEY HAVE NO REASON TO STOP.

And they’re still not running out of stupid ideas we can see through:

UPDATE 3: OCTOBER 17 2021:

TOLD YA!

Guess who has a vaccine in works for it

Oh, look who pushes the fear! Exactly who I would’ve expected:

Later update: In the meantime I’ve learned that Marburg (an Ebola relative) and Xinjiang fever, a Chinese relative of the Yellow Fever virus, are also top candidates, and that goes in line with the Fauci e-mails I highlighted below. I will be back with more details shortly. Almost certainly it will be some form of hemorrhagic fever, most likely to cover for injections side-effects on the blood stream.

UPDATE 2:

One month later, they’re starting to catch up and it’s still not too late to un-play it if this goes BOOM NOW!



By the end of last century, The Military has abandoned you and has joined Pharmafia and the super-rich elites in a plan to govern you with bioweapons and psy-ops. As I’ve said many times, Big Pharma and Big Tech are long gone, The Military BioTech Complex has been running the show for quite a while.
This is just a chapter from that book, more to come if we get some love.

WHAT YOU NEED TO KNOW:

INDIA BLACKLISTED US CDC FOR SECRETLY FUNDING BIOWEAPONS RESEARCH IN MANIPAL – Silview.media

Government pulls up U.S. agency for work on Nipah virus – The Hindu

NIPAH IS ONE OF THREE VIRUSES MODIFIED BY WUHAN LAB AT NIAD’S REQUEST, FAUCI E-MAIL REVEAL – Silview.media

SOURCE

Canadian lab’s shipment of Ebola, Henipah viruses to China raises questions

  • Henipah and Nipah are interchangeable

Scientists at the National Microbiology Lab sent live Ebola and Henipah viruses to Beijing on an Air Canada flight March 31, and while the Public Health Agency of Canada says all federal policies were followed, there are questions about whether that shipment is part of an ongoing RCMP investigation.

Ebola and Henipah are Level 4 pathogens, meaning they’re some of the deadliest viruses in the world. They must be contained in a lab with the highest level of biosafety control, such as the one in Winnipeg. 

Two months after that shipment, on May 24, the Public Health Agency of Canada (PHAC) referred an “administrative matter” to RCMP that resulted in the removal of two Chinese research scientists — Xiangguo Qiu and Keding Cheng — and several international students on July 5. 

Both agencies have said repeatedly that public safety has not been at risk. 

PHAC will not confirm if the March 31 shipment is part of the RCMP investigation.

Strict protocols

Several sources, who have asked to remain anonymous because they fear for their jobs, say the pathogens may have been shipped to the Chinese Academy of Sciences in a way that circumvented the lab’s operating procedures, and without a document protecting Canada’s intellectual property rights.

Researchers working at the National Microbiology Lab on cutting-edge, high-containment research are not allowed to send anything to other countries or labs without the intellectual property office negotiating and having a material transfer agreement in place, in case the material sent leads to a notable discovery.

A PHAC spokesperson did not confirm if this shipment included such an agreement.

However, Eric Morrissette said it’s “routine” for the lab to share samples of pathogens and toxins with partners in other countries to advance scientific work worldwide.

The transfers follow strict protocols, including requirements under the Human Pathogens and Toxins Act(HPTA), the Transportation of Dangerous Goods Act, theCanadian Biosafety Standard and the lab’s standard operating procedures, Morrisette added.

“All transfers of Risk Group 4 samples follow strict transportation requirements and are authorized by senior officials at the lab and the NML tracks and keeps electronic records of all shipments of samples in accordance with the HPTA. Agreements for the transfer of materials are determined on a case-by-case basis,” Morrisette wrote in an email statement.

“On the specific shipments to China earlier this year, we can confirm that we have all records pertaining to the shipment, and that all protocols were followed as directed by the above Acts and Standards.”

Sources say Xiangguo Qiu and her husband, Keding Cheng, were escorted from the National Microbiology Lab in Winnipeg on July 5. (Governor General’s Innovation Awards)

Xiangguo Qiu is head of the National Microbiology Lab’s Vaccine Development and Antiviral Therapies section in the Special Pathogens Program. She is responsible for the lab that works with Ebola. Her husband, Keding Cheng, is also a PHAC biologist. 

After their security clearance was revoked and they were escorted from the lab, the University of Manitoba also cut ties with them and re-assigned Qiu’s graduate students, pending the RCMP investigation. No charges have been laid.

Neither scientist has responded to requests for comment, although some of their former colleagues say Qiu is not just a world-renowned scientist who helped develop a treatment for Ebola, but also a researcher with ethics and integrity.

Case raises questions 

One question raised by this case is that of intellectual property protection, says Leah West, who practises, studies and publishes in the field of national security law and lectures at the Norman Paterson School of International Affairs.

“If China was leveraging these scientists in Canada to gain access to a potentially valuable pathogen or to elements of a virus without having to license the patent  … it makes sense with the idea of China trying to gain access to valuable IP without paying for it,” she said.

Leah West says she hopes the lab and Health Canada are doing an investigation in addition to the one the RCMP is conducting. (Submitted by Leah West)

West accepts PHAC’s assertion that public safety is not an issue, even though the viruses were transported on a commercial Air Canada flight.

However, she says the fact the RCMP is involved means there’s a legitimate concern.

“You don’t send a policy breach, a bureaucratic policy breach, to the RCMP to investigate unless you believe that that policy breach has resulted in a criminal offence or could have resulted in a criminal offence. So what is the criminal offence potentially here?” West said.

She said she hopes the lab and Health Canada are also doing an internal investigation.

“I think there will need to be an inquiry into the scientists to potentially see whether or not they were compromised or any elements of their work were compromised and that China gained illegal or improper access to Canadian intellectual property … to see what China may have gained access to without knowledge, prior to this incident,” West says.

Don’t ‘jump into any conclusions too quickly’

However, the deputy director of the University of Alberta’s China Institute is urging caution when it comes to making assumptions. 

Jia Wang doesn’t dispute China has been involved in the past in espionage and intellectual property theft, but she says that country is making big investments in developing STEM (science, technology, engineering and mathematics) scholars and then putting that into innovation.

China has its own reasons to protect intellectual property because many new ideas are coming from there, Wang says.

She’s waiting to see what comes of the RCMP investigation of the lab in Winnipeg.

“As China observers, we’d like to perhaps gently remind people not to jump into any conclusions too quickly,” she said.

“It will be good to get to the bottom of this and see what might have gone wrong and what was the oversight and how can the procedures be improved or people involved can be reminded of how to adhere to the policies better.”

Jia Wang, deputy director of the University of Alberta’s China Institute, is advising caution about making assumptions concerning the case. (Submitted by Jia Wang)

The shipment of the viruses took place at a time when relations between Canada and China have been strained over the arrest of a Huawei executive, at the request of the United States. 

In retaliation, China has detained two Canadians and is boycotting Canadian canola and pork.

Because of the strained relationship between the two countries, and this case at the lab, Chinese-Canadian researchers and academics are starting to worry they may be singled out and targeted, Wang said.

“Certain assumptions are made or their loyalty to Canada is questioned in any way. And as multicultural as we are in Canada, we don’t want to see that.”  – CBC, 2019

SOURCE

On December 19, 2019, the U.S. Food and Drug Administration announced the approval of Ervebo to prevent EVD caused by Zaire ebolavirus in individuals 18 years of age and older. This report, published by the U.S. CDC on January 8, 2021, summarizes the Advisory Committee on Immunization Practices (ACIP) recommendations for using the rVSVΔG-ZEBOV-GP Ebola vaccine (Ervebo) in the USA.

On July 1, 2020, the European Medicines Agency granted Johnson & Johnson Janssen’s Zabdeno and Mvabea Ebola vaccine therapy, a prime-boost vaccination approach for preventing infectious diseases. Janssen’s Ebola vaccine regimen is specifically designed to induce long-term immunity against the Ebola virus in adults and children aged one year and above.

CanSino Biologics’s Ad5-EBOV Ebola vaccine received approval in China in October 2017. Ad5-EBOV is an adenovirus type 5 vector-based Ebola virus disease vaccine that protects against Ebola by relying on the recombinant replication-defective human adenovirus type-5 vector immune response. In addition, Ad5-EBOV is manufactured as a lyophilized powder, highly stable, and does not require storage at ultra-low temperatures. This feature renders it viable for use in resource-limited tropical areas.

The WHO published the revised Ebola Vaccine FAQ on January 11, 2020.

In 2019, World’s deadliest viruses were ‘shipped to Wuhan ‘leak lab’ from Canada by rogue scientists linked to Chinese military’ – The Sun

Experts Say Nipah Virus Has Potential To Be Another Pandemic — With A Higher Death Toll – Yahoo

What is Henipavirus?

Henipaviruses belong to the family of paramyxoviruses. Two species have been identified to be zoonotic, causing disease in animals. These are the Hendra virus (HeV) and the Nipah virus (NiV). They produce severe and often fatal illness in humans and horses.

News-Medical.net

THAT IS TO SAY ‘NIPAH’, ‘HENIPAH’ AND ‘HENIPAVIRUS’ ARE INTERCHANGEABLE HERE

Samples from early Wuhan COVID-19 patients show the presence of genetically modified Henipah virus, an American scientist has found.

Henipah was one of the two types of viruses sent to China by Chinese-born scientists from a Canadian laboratory at the centre of a controversy over the firing of the scientists and collaboration with Chinese military researchers. It is not clear whether the virus found in the Chinese samples is related to the samples sent by the Canadian lab, which were shipped in late March 2019.

The finding was confirmed for The Epoch Times by another qualified scientist.

The evidence was first found by Dr. Steven Quay, a Seattle-based physician-scientist and former faculty member at the Stanford University School of Medicine, who looked at early COVID-19 samples uploaded by scientists at the Wuhan Institute of Virology (WIV) shortly after China informed the World Health Organization about the SARS-CoV-2 outbreak.

Epoch Times Photo
Chinese virologist Shi Zhengli is seen inside the P4 laboratory in Wuhan, China, on Feb. 23, 2017. (Johannes Eisele/AFP via Getty Images)

The samples from the patients, who reportedly were found to have the “unknown pneumonia” in December 2019, were uploaded to the genetic sequence database, GenBank, on the website of the U.S. National Institute of Health (NIH).

Quay says that while other scientists around the world were mostly interested in examining the genome of SARS-CoV-2 in the samples uploaded by the WIV scientists, he wanted to see what else was in the samples collected from the patients.

So he collaborated with a few other scientists to analyze sequences from the samples.

“We started fishing inside for weird things,” Quay told The Epoch Times.

What they found, he says, are the results of what could likely be contamination from different experiments in the lab making their way into the samples, as well as evidence of Henipah virus.

“We found genetic manipulation of the Nipah virus, which is more lethal than Ebola.” Nipah is a type of Henipah virus.

The Epoch Times asked Joe Wang, PhD, who formerly spearheaded a vaccine development program for SARS in Canada with one of the world’s leading pharmaceutical companies, to verify the finding. Wang is currently the president of NTD Television Canada, the sister company of The Epoch Times in Canada.

After examining the evidence, Wang said he was able to replicate Quay’s findings on the Henipah virus. He explains that the genetic manipulation of the virus was likely for the purposes of vaccine development.

Winnipeg Lab

The firing of Chinese-born scientist Xiangguo Qiu and her husband, Keding Cheng, from the National Microbiology laboratory (NML) in Winnipeg has been the subject of much controversy in Canada, with opposition parties pressing the government for more details on the case, and the government refusing to release information citing national security and privacy concerns.

Qiu and Cheng along with several Chinese students were escorted out of NML, Canada’s only Level 4 lab, in July 2019, amid a police investigation. The two scientists were formally fired in January 2021.

The Public Health Agency of Canada (PHAC), which is in charge of NML, said the termination was the result of an “administrative matter” and “possible breaches of security protocols,” but has declined to provide further details, citing security and privacy concerns.

Epoch Times Photo
House Speaker Anthony Rota admonishes Public Health Agency of Canada President Iain Stewart in the House of Commons on June 21, 2021, for failing to provide documents related to the firing of two scientists from the National Microbiology Laboratory in Winnipeg. (The Canadian Press/Sean Kilpatrick)

During her time at NML, Qiu travelled several times in an official capacity to WIV, helping train personnel on Level 4 safety. The Globe and Mail later reported that scientists at NML have been collaborating with Chinese military researchers on deadly pathogens, and that one of the Chinese military researchers worked at the high-security Winnipeg lab for a period of time.

Documents and emails released by PHAC show that the shipment of Henipah and Ebola samples was done with the permission of NML authorities.

In one of the emails sent in September 2018, David Safronetz, chief of special pathogens at PHAC, informs then-head of NML Matthew Gilmour and other lab administrators about the request from WIV for the shipment of the samples, saying “I trust the lab.”

In response, Gilmour asks about the nature of the work that will be done at the Wuhan lab, and why the lab doesn’t get the material from “other, more local labs.” He also tells Safronetz that it’s “good to know that you trust this group,” asking how NML was connected with them.

In his reply, Safronetz doesn’t specifically say what the samples will be used for in China, but notes they will only be sent once all paperwork and certification is completed. He also says the WIV is requesting the material from NML “due to collaboration” with Qiu.

He adds, “Historically, it’s also been easier to obtain material from us as opposed to US labs. I don’t think other, closer labs have the ability to ship these materials.”

Gilmour resigned from his position at NML in May 2020 and joined a UK-based bioresearch company.

MPs have asked NML management why shipment of the samples was allowed and whether they knew if China performs any Gain of Function (GoF) research at WIV. GoF research involves increasing the lethal level (virulence) or transmissibility of pathogens.

NML’s acting scientific director general Guillaume Poliquin told MPs during a parliamentary committee meeting on March 22 that the lab only sent the samples to WIV after receiving assurance that no GoF research would take place.

Conservative MP John Williamson pressed for more answers, saying the word of the state-run Chinese lab can’t be trusted as the Chinese regime “has a history of theft and lies.”

The issue of GoF research at WIV has been a point of contention in the United States between lawmakers and Dr. Anthony Fauci, NIH’s head of the National Institute of Allergy and Infectious Diseases, whose organization has funded research (through EcoHealth Alliance) on coronaviruses at the Wuhan lab. U.S. Sen. Rand Paul says published work from WIV on coronaviruses shows the lab is conducting GoF research, a charge Fauci denies.

Epoch Times Photo
The P4 laboratory on the campus of the Wuhan Institute of Virology in Wuhan, China, on May 13, 2020. (Hector Retamal/AFP via Getty Images)

The Epoch Times sought comment from PHAC, including as to how the agency addressed issues of intellectual property and the development of any products such as vaccines with WIV, but didn’t hear back by time of publication.

Despite repeated requests by opposition parties for more details related to the firing of the two NML scientists, the Liberal government has refused to provide records, saying there are national security and privacy concerns.

After the House of Commons issued an order for the government to disclose the information, the government took the Speaker of the House to court to obtain confirmation from a judge that it can withhold the documents. The government later dropped its court case once Prime Minister Justin Trudeau called an election and Parliament was dissolved. – Epoch Times

LATER UPDATE: JUST LEARNED NIPAH WAS THE INSPIRATION FOR ANOTHER DRILL VERY SIMILAR TO EVENT201 – CLADE-X

NOTEWORTHY: Germany is the epicenter of this psyop, in their scenario

‘For the next pandemic, we’ll have gigantic mRNA factories in India’ – Bill Gates

The next pandemic: Nipah virus? – Bill Gates’ GAVI

SOURCE

Oh, look, a Dutch NGO on Taiwan TV pushing Nipah fearporn to WHO as early as February 2021:

SOURCE

India fighting to contain Nipah, a virus deadlier than COVID-19 – NY Post

Experimental drug by Gilead completely effective against Nipah virus infection in monkeys – NIH

ALSO IN 2019, INDIA CONDUCTS NIPAH OUTBREAK DRILLS. OFFICIALS SAY THEY HOPE FOR FULL PREPAREDNESS BY 2022:

ECO-HEALTH ALLIANCE INVOLVED AGAIN!

Remember the host?

THERE ARE SEVERAL PATENTS FOR NIPAH DRUGS AND SOME ARE mRNA GENE THERAPIES REGISTERED AS VACCINES

SOURCE
SOURCE
SOURCE

UPDATE 3: I FOUND CREDIBLE SOURCES FOR MOST OF DR. ARYANA LOVE’S EXPLOSIVE CLAIMS BELOW:

I didn’t have an in depth look at all her sources, I can’t have a final 100% verdict, but I did more than a glance and no lies detected. You can review her blog post yourself HERE.
This might be the closure to this report and the start for another.

BONUS

This is from 2014m but the story goes a way long back. And forward. Let’s not forget Putin is a Davos regular since before he became such a literal czar.

‘Contagion’ Reality Check: CDC Experts Explore Some of the Film’s Scenarios – PBS

WE ARE BEING PRIMED FOR THE DARKEST WINTER

To be continued?
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We hardly made it before, but this summer something’s going on, our audience stats show bizarre patterns, we’re severely under estimates and the last savings are gone. We’re not your responsibility, but if you find enough benefits in this work…
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! Articles can always be subject of later editing as a way of perfecting them

The rare media reports on this case only mention WHO’s chief scientist, but after obtaining the original legal notice from IBA, we find out that Tedros and one more doctor are equally indicted.
The best part is that they repeatedly use the term “conspiracy”, and, finally, someone uses it correctly.

Quick update as of July 14th, 2021:
I’ve just learned of two more similar court cases that also involve Bill Gates, Fauci and GAVI, among others. Currently analyzing the documents and digging for more info. I will report more ASAP.

LEGAL NOTICE FOR CONTEMPT OF COURT AGAINST DR. TEDROS ADHANOM GHEBREYESUS, DR. SOUMYA SWAMINATHAN AND THE DIRECTORATE GENERAL OF HEALTH SERVICES (DGHS)

POSTED BY INDIAN BAR ASSOCIATION ON  WITH 0 COMMENT

LEGAL NOTICE FOR CONTEMPT OF COURT AGAINST DR. TEDROS ADHANOM GHEBREYESUS, DR. SOUMYA SWAMINATHAN AND THE DIRECTORATE GENERAL OF HEALTH SERVICES (DGHS)

The accused are served legal notice for their attempt to undermine the authority of the Bombay High Court and obstruct the use of Ivermectin for Covid-19 treatment.

DOWNLOAD

On 13th June 2021, Indian Bar Association has served a notice upon Dr.Tedros Adhanom Ghebreyesus, Director General, World Health Organisation, Dr.Soumya  Swaminathan, the Chief Scientist at WHO and Prof. (Dr.) Sunil Kumar for contempt of judgment of Bombay High Court.

The Bombay High Court vide its judgment dated 28th May 2021 has already given a green signal for use of Ivermectin for treatment of Covid-19.

Despite this, all the three contemnors have hatched a conspiracy and by spreading misinformation through media, are fuelling confusion amongst doctors by introducing Guidelines allegedly published on 27th May 2021 by DGHS, which are in fact not mandatory and are overruled by the judgment of Bombay High Court dated 28thMay 2021.

The State Government of Goa, in their affidavit filed before Bombay High Court, has specifically pointed out that the WHO advisory against the use of Ivermectin is flawed and the research showed that the Ivermectin is effective for treatment of COVID-19. The Bombay High Court on 28th May 2021, after considering WHO advisory and all other contentions of the rival parties, came to the conclusion that the use of Ivermectin cannot be stopped. The High Court has also taken the note of the guidelines dated 17th May 2021 issued by Indian Council of Medical Research (ICMR), thereby advocating the use of Ivermectin.

Thereafter, a detailed and impactful article was published by the leading newspaper ‘Free Press Journal’ on 6th June 2021 (updated on 14th June 2021) wherein the author has articulated very well as to how the advisories of WHO are dubious.

https://www.freepressjournal.in/india/covid-19-are-whos-directives-being-taken-seriously-on-the-ground

Surprisingly, in its first, the Directorate of Health Services (DGHA) on 27th May, 2021 announced ‘Comprehensive Guidelines for Management of COVID-19 patients’ which excludes Ivermectin and several popular drugs.

It is worthwhile to note that DGHS is a repository of technical knowledge and is an attached organisation of the Ministry of Health & Family Welfare. The Guidelines/National Protocol have always been issued by the Joint Task Force of All India Institute of Medical Science (AIIMS) and Indian Council for Medical Research (ICMR) under the aegis of Government of India. Moreover, the document containing these impugned Guidelines does mention version/date and does not carry logos of Government of India, ICMR and AIIMS,suggesting lack of consensus between DGHS and the Joint Task Force.

Now, in order to diminish the impact of the article published on 6th June, 2021, the main accused Dr. Soumya Swaminathan hatched a conspiracy and managed some media houses to publish news on 7th June, 2021 for appreciating the overruled guidelines dated 27th May, 2021. Some of these media houses have showed astounding alacrity in publishing news hailing removal of Ivermectin and other drugs, thereby deliberately ignoring the mountains of clinical data on effectiveness of Ivermectin in treatment of COVID-19.

These impugned Guidelines issued by DGHS were circulated first on 7th June 2021, without any mention of the judgment of Bombay High Court dated 28thMay, 2021, which in fact is against the said guidelines, rendering these guidelines as null and void.

As per the judgment of Supreme Court of India, the person responsible for spreading information with object of creating confusion and to obstruct and undermine the judgment of court is liable for punishment under contempt of Court. Sections like 505,192,302, 115,109,409,120(B) of the Indian Penal Code are also attracted against the accused in this case, as their intention was to kill several people to fulfil their ulterior purposes.

The maximum punishment in above cases is death penalty.

The notice states that Dr. Soumya Swaminathan and the WHO are dishonest and have no scientific evidences to back their advisories and such loose statements are issued from time to time, to serve their ulterior purposes.

The relevant part of the notice reads this:

“53.1. Each time and particularly from following specific instances, it is sufficiently proved that You Notice 1 & 2 do not possess any authentic and scientific evidences;

i) When the earlier Notice was served on Notice 1 on 25.05.2021, she has neither replied to the notice nor has she approached any court of law against us. On the contrary, she chose to delete the controversial tweet advising against the use of Ivermectin for COVID-19;

ii) When the Health Secretary of the State Government of Goa relying on affidavit of Under Secretary of Union of India made their submission on oath before Hon’ble High Court, with specific allegations against WHO that there are reports which have observed that the analysis by WHO on this medicine (IVERMECTIN) is flawed and that the mortality rate is actually much lower if the said medicine is used for early treatment as well as prophylaxisneither you Notice 1 or 2 chose to produce any proof to counter the said report. As a result, Hon’ble High Court has refused to accept the advisory of WHO.

iii) When All India Institute of Medical Science (AIIMS) had published a statement on 24.05.2021 that there is no evidence to predict the third wave and its effect on children, you Notice 1 did not give any “Evidence” in support of your statement dated 25.05.2021 which was contrary to the said statement of AIIMS.

After you Notice 1 were served with legal notice on 25.05.2021, you feared for being exposed and being summoned in Court of Law and therefore you Notice 1 took a U turn and stated that there is no sufficient evidence to suggest that children would be affected in the third wave.

The agenda of misinformation is also exposed in the statement published in Press Bureau of India on June 8, 2021

“It is a piece of misinformation that subsequent waves of the COVID-19 pandemic are going to cause severe illness in children. There is no data – either from India or globally – to show that children will be seriously infected in subsequent waves.”

53.2. So it is crystal clear that You Notice 1 & 2 do not have scientific evidence except jugglery of words and you are thoroughly intellectually dishonest people who are playing with the lives and livelihood of the common people across the world.

However, in order to expose your intellectual dishonesty to the entire world, this notice is being served, calling for an explanation within 7 days of the receipt of this notice.”

The legal notice also explains the law of damages in India citing recently cases where Court had ordered compensation of Rs. 100 Crores ((USD 13.5 mn) to the aggrieved party, for loss of his reputation. Since the present matter involves death caused due to denial of early treatment resulting in deterioration and death of person, the damages claimed would be much higher that Rs. 100 Crores.

The notice also explains the liability of Dr. Tedros Adhanom Ghebreyesus, Director General of WHO, for his act of commission and omission and also for his implied consent to the conspiracy.

In the similar manner, the DGHS Prof. (Dr.) Sunil Kumar is joined in as co-accused for his complicity in the conspiracy.

The three possible explanations for such an intense opposition to the use of highly promising, well-tolerated off-label medicine as Ivermectin are explained very well in following article:

WHO Celebrates As Indian Health Regulator Removes Ivermectin from Its Covid-19 Protocol | naked capitalism

  • “As a generic, Ivermectin is cheap and widely available, which means there would be a lot less money to be made by Big Pharma if it became the go-to early-stage treatment against covid.
  • Other pharmaceutical companies are developing their own novel treatments for Covid-19 which would have to compete directly with Ivermectin.
  • If approved as a covid-19 treatment, Ivermectin could even threaten the Emergency Use Authorisation granted to covid-19 vaccines.

It’s worth noting that while India’s DGHS has dumped most cheap off-patent treatment options against Covid, including even multivitamins, more expensive patented medicines continue to get the green light. They include Gilead’s prohibitively expensive antiviral Remdesivir, which DGHS continues to recommend for “select moderate/ severe hospitalised COVID-19 patients”, even though “it is only an experimental drug with potential to harm.” It has also authorised the use of the anti-inflammatory medicine to cilizumab, which costs hundreds of dollars a dose.” – IBA

I’m not very optimistic, I see this as another attempt to cement the existence of a fake virus in the collective mental, but either way this goes, the implications are huge.
Consider that WHO didn’t act alone, Big Tech, mass-mediots and politicians would be affected by the same logic and principles.
And if this falls flat, it’s only going to signal more corruption to the general population.

BUT, MOST IMPORTANTLY, IF THESE DRUGS ARE OFFICIALLY RECOGNIZED AS EFFICIENT AGAINST COVID-19, THEN THERE HAS NEVER BEEN A LEGAL BASIS FOR EMERGENCY STATES / EMERGENCY AUTHORIZATIONS FOR EXPERIMENTAL INJECTIONS DISGUISED AS VACCINES

If approved as a covid-19 treatment, Ivermectin could even threaten the Emergency Use Authorisation granted to covid-19 vaccines.

IBA

Demand from India to #ArrestDrTedros grows louder on social media

Goa Chronicle 11/04/20200 

 Dr Tedros Adhanom Ghebreyesus, Director-General, World Health Organisation

Panjim: The call from journalist and social activist Savio Rodrigues encouraging people of India to raise their voices on social media platform Twitter demanding arrest Dr Tedros Adhanom Ghebreyesus is growing louder.

#ArrestDrTedros is currently trending in India.

Savio Rodrigues is the Founder & Editor-in-Chief of GoaChronicle.com. The online new portal has been exposing the complicit role of Dr Tedros during the coronavirus pandemic due to his closeness with China. In fact, Rodrigues, opines that China backed Dr Tedros to the position of Director-General of the World Health Organisation (WHO) and Dr Tedros in turn was China’s puppet in WHO

Rodrigues in his several informative articles has raised questions on the dereliction of duty and cover-up of China’s questionable actions by the Director-General of (WHO).

Earlier today Rodrigues called for the people of India to unite and demand for the arrest of Dr Tedros, post the publishing of his article:

https://goachronicle.com/dr-tedros-must-be-arrested/

He took to social media platform Twitter stating:

Here are some of the Twitter messages demanding #ArrestDrTedros

https://twitter.com/nitinpurandare/status/1248922807506849792?s=20

Rodrigues opines : “The World Health Organisation under the leadership of its Director-General Dr Tedros Adhanom Ghebreyesus failed in its core responsibility to detect a health crisis and contain the spread of this contagious virus globally.

It instead chose to side with China – the nation from which the coronavirus originates and was the first epicentre of the virus. It is from Wuhan, China that the China Virus has spread globally to reportedly 180 countries.

We can go pontificating on different theories of the blame game. The political leaders can continue to play their own political games. Nothing will ever change the truth.

The truth is that this is a virus that has come out of a lab. The truth is that China had knowledge about its human-to-human transmission as early as December. The truth is that Dr Tedros relied on  the report of the Chinese Health Authorities in his statement on January 14, 2020, “No clear evidence of human-to-human transmission. The truth is that China has withdrawn the lockdown in Wuhan and city is back to normal business will the rest of the world is under lockdown.

But the most horrific truth is people are dying. They will continue to die. We have crossed 100,000 deaths but the count will not cease, it will only keep on increasing.”

Whether Dr Tedros is arrested is a question that can only be in answered in time but what is important to state the noise to get him to step down from his post is certainly getting louder.

Tedros is met with treason and genocide accusations even in his own country, Ethiopia, but the government there simply doesn’t have the balls to anger Tedros’ allies issuing and arrest warrant to complete the investigation. However, the chief of Ethiopian military, as well as much of Indian media and population, don’t seem to hold back anymore. It’s doubtful he’s ever going to step home again.

WHO Celebrates As Indian Health Regulator Removes Ivermectin from Its Covid-19 Protocol

Posted on  by Naked Capitalism

After India finally gets somewhat of a grip on its deadly second wave, one of its health regulators just took away one of its main lines of defense. 

India’s Directorate General of Health Services (DGHS) has executed a policy reversal that could have massive implications for the battle against covid-19, not only in India but around the world. Hundreds of thousands, if not millions of lives, could be at stake. The health regulator has overhauled its COVID-19 treatment guidelines and removed almost all of the repurposed medicines it had previously recommended for treating asymptomatic and mild cases. They include the antibiotic doxycycline, hydroxychloroquine, zinc, ivermectin and even multivitamins. The only medicines that are still recommended for early treatment are cold medicines, antipyretics such as paracetamol and inhaled budesonide.

“No other covid-specific medication [is] required,” say the new guidelines, which also discourage practitioners from prescribing unnecessary tests such as CT scans.

“Patients are advised to seek tele consultation; and Covid-19 appropriate behaviour must be observed such as mask, strict hand hygiene and physical distancing… [Patients are also advised to maintain] a healthy diet with proper hydration… [and] to stay connected [with family] and engage in positive talks through phone, video-calls, etc.”

The decision to remove ivermectin, multivitamins and zinc from the treatment guidelines is hard to comprehend given the current state of play in India — unless one assumes foul play. After suffering one of the worst covid-19 outbreaks since the pandemic began, resulting in the loss of hundreds of thousands of lives, India is not just flattening the curve, it is crushing it. And the widespread use of ivermectin, a potent anti-viral and anti-inflammatory with an excellent safety profile, appears to have played an instrumental role.

WHO’s Happy

Other countries in the region have already taken notice. Indonesia just approved the use of ivermectin in Kudus, a local contagion hotspot. 

This is the last thing the World Health Organization (WHO) and the pharmaceutical companies whose interests it broadly represents want. As such, it was no surprise that WHO was delighted with the DGHS’ policy reversal. “Evidence based guidelines from @mohfw DGHS – simple, rational and clear guidance for physicians,” tweeted WHO’s chief scientist Soumya Swaminathan, of Indian descent. “Should be translated and disseminated in all Indian languages.”

As I posited in my recent article “I Don’t Know of a Bigger Story in the World” Right Now Than Ivermectin: NY Times Best-Selling Author, there are three possible explanations for global health regulators’ opposition to the use of a highly promising, well-tolerated off-label medicine such as ivermectin:

  • As a generic, ivermectin is cheap and widely available, which means there would be a lot less money to be made by Big Pharma if it became the go-to early-stage treatment against covid.
  • Other pharmaceutical companies are developing their own novel treatments for Covid-19 which would have to compete directly with ivermectin.  
  • If approved as a covid-19 treatment, ivermectin could even threaten the emergency use authorisation granted to covid-19 vaccines

It’s worth noting that while India’s DGHS has dumped most cheap off-patent treatment options against Covid, including even multivitamins, more expensive patented medicines continue to get the green light. They include Gilead’s prohibitively expensive antiviral Remdesivir, which DGHS  continues to recommend for “select moderate/ severe hospitalised COVID-19 patients”, even though “it is only an experimental drug with potential to harm.” It has also authorised the use of the anti-inflammatory medicine tocilizumab, which costs hundreds of dollars a dose.

Crushing the Curve

The DGHS began recommending the widespread use of ivermectin as early as April, in direct contradiction of the recommendations of the World Health Organization. Treatment packs were assembled in many states and distributed to patients testing positive for Covid. In at least two states — Goa and Uttarakhand — the medicine was distributed as a preventive. As has already happened in over 20 countries where ivermectin has been used — from Mexico, the Dominican Republic and Peru to Slovakia, the Czech Republic and Bangladesh — case numbers, hospitalizations and fatalities have fallen in almost vertical fashion. On Monday the country recorded its lowest number of new cases in 61 days.

“When we started seeing more cases, we decided to take up a door-to-door survey,” Bagalkot District Health Officer Dr Ananth Desai told New India Express. “When the health officials noticed people with symptoms during the survey, they tested them immediately and provided them with home isolation kits, which had medicines like Ivermectin, calcium and zinc tablets along with paracetamol. We advised the patients to start with the medication even before their Covid-19 test results came out. With these measures, we noticed that many patients recovered faster. This helped in increasing the recovery rate”.

In India’s capital, Delhi, the number of people testing positive for Covid-19 daily has fallen 97% from a peak of 24,000 on April 24. The number of deaths is down by around 85%. Only 17% of the total beds earmarked for Covid-19 treatment in Delhi and around 40% of the ICU beds were occupied late last week, according to the government’s Delhi Corona app. At the peak, there were days when no ICU beds were available in the city.

Imagen

Out of the Darkness, But For How Long?

Just over four weeks ago India was in a very dark place. At one point it was accounting for almost half of all global cases and one in every four covid-19 deaths. The government had lost complete control. Four weeks later, the country, while not out of the woods, is in a much better place. While the official numbers of cases and deaths are probably still a fraction of the real numbers, the trend is clearly moving in the right direction.

An important reason for that is that doctors in India have been treating covid patients as early as possible — something that isn’t happening in most countries, particularly rich ones that play an outsized role in setting global health policy. In India early treatment has helped to reduce the number of cases becoming acute. And that has helped to reduce the pressure on hospitals and vital resources such as oxygen. Ivermectin also appears to have helped reduce the spread of the virus, thanks to its potent anti-viral properties.

Just about everywhere ivermectin is used, the number of cases, hospitalizations and deaths fall precipitously. Of course, this is only a temporal correlation. But nonetheless a clear pattern across nations and territories has formed that strongly supports ivermectin’s purported efficacy. And that efficacy has been amply demonstrated in dozens of clinical studies and multiple meta-analyses. But it’s not proof enough for global health authorities, which have set the bar for ivermectin so high that it’s almost impossible to straddle. 

Of course, other factors such as lockdowns, travel restrictions and increased herd immunity have also played a part in India’s rapid turnaround. But vaccines’ role has been minimal given that just 16 doses have been administered per hundred people. It’s going to take many more months, if not longer, to vaccinate a majority of the population. In the meantime, hundreds of millions of people will remain unprotected from the virus. Many will end up catching and transmitting it. Yet the Directorate General of Health Services has taken away one of the country’s only lines of defense.

It remains to be seen whether state governors and health bureaucrats will comply with the recommendations. For the moment the separate treatment protocols recommended by India’s Ministry of Health and Family Welfare (MOHFW) and the Indian Council of Medical Research (ICMR) continue to include ivermectin. As such, many doctors are likely to continue prescribing the medicine. But what happens if MOHFW and ICMR follow the DGHS’ lead and also drop ivermectin. Will doctors stop using a medicine they know to work against a virus that has already caused so much devastation?

India’s most populous state, Uttar Pradesh, has been using ivermectin since last summer. In this second wave the turnaround was so dramatic that even the World Health Organization (WHO) showcased its achievements. In a May 7 article titled “Going the Last Mile to Stop Covid-19” the WHO noted that aggressive population-wide health schemes, including home testing and “medicine kits”, had helped regain control of the virus. But what the WHO failed to mention is what was in those medicine kits.

Instead, three days later WHO’s chief scientist Soumya Swaminathan, of Indian descent, tweeted out a reminder that ivermectin is not recommended to treat covid-19 patients. The tweet included a press release issued by the company that manufactures the drug, Merck, saying it had found no evidence to support the use of ivermectin in the treatment of COVID-19. Merck, it’s worth recalling, is developing an antiviral compound, molnupiravir, that will have to compete directly with ivermectin, one of the cheapest, safest drugs on the planet — unless, of course, ivermectin is taken out of the picture.

A Cautionary Tale

But if that happens, the result is likely to be a lot more deaths. Peru, the first country to use ivermectin against Covid, is living proof of that. The medicine was first used in eight states during the very early stages of the pandemic (May-July). After showing promise, it was extended to the whole country. Excess deaths dropped 59% (25%) at +30 days and 75% (25%) at +45 days after day of peak deaths. But in October, after the first wave had been brought under control, a newly elected government in Lima took the inexplicable step of withdrawing a number of medicines, including ivermectin, from its treatment guide for the disease.

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Within weeks hospitalizations and deaths were soaring once again. The graph above, taken from a study by Juan Chamie, Jennifer Hibberd of the University of Toronto and David Scheim of the US Public Health Service, shows the sharp rise, fall and resurgence in excess deaths (among the over 60 year-old cohort) in Peru as the virus waxed, waned and waxed again. Since Peru dropped ivermectin the virus has raged through the population. Peru now has the highest per-capita death rate from covid on the planet. It’s a cautionary tale that India, with a population more than 30 times that of Peru, would do well to heed.


To be updated

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This is a corroboration of a few recent reports from various news outlets in India and external sources. We face another grave under-reported fact in a “top-shelf authoritative source” CV. Or CR. The ramifications are vast.
We have much more of these to disclose in the near future.

<< India has asked the American frontline public health agency, the Centre for Disease Control and Prevention (CDC) to stop funding virus research studies in the country. CDC was caught funding Karnataka’s Manipal Center for Virus Research (MCVR) for secretly carrying out research on the lethal Nipah virus – a pathogen considered potential bioweapon. The fact that an under-qualified private laboratory was secretly handling a dangerous virus under government’s nose at the behest of a foreign agency has raised major concerns within the health ministry apparatus.

The matter is more complicated with the fact that the CDC has a checkered history in India. The Indian defense establishment believes that the CDC was involved in the plague outbreak in the western Indian city of Surat in 1994, which they consider to be a case of bioterrorism. Earlier in February this year the Indian government launched an investigation into another secret research being conducted on bat hunters in the eastern Indian state of Nagaland, funded by the US Department of Defense in collaboration with Wuhan Institute of Virology and the Bill and Melinda Gates Foundation.

CDC put on Watchlist

A $3.6 million donation from Atlanta-based US health agency CDC to Indian research agencies for tackling the COVID-19 pandemic has been put on hold by the Ministry of Home Affairs (MHA). The CDC has been placed on the watchlist since December 2019 for its involvement in funding virus research without government’s approval.

The Nipah research fiasco that came into light in October last year was the primary reason behind the MHA decision. As of now, any funding or donation from the U.S government body CDC would be first cleared by the MHA itself. They can no longer send funds directly to any government or private institution in India without MHA’s clearance.

No translation availables, sorry!

CDC secretly funds risky virus research in India

In October 2019, Hindustan Times reported that the Union health ministry wrote to both CDC and Manipal Center for Virus Research, ordering them to shut down the study related to Nipah virus that belongs to Risk Group 4 (RG4) classification. The RG4 viruses are considered highly dangerous and have no treatment or vaccine. They can only be tested in BSL4 lab which is the highest level of biological safety. The health ministry was upset that a study related to high risk pathogens like Nipah was being carried out at MCVR which is BSL2+ level facility.

A memorandum sent out by the health ministry said:

“It has been brought to our notice that CDC had trained MCVR for diagnosis of Nipah virus disease (NIV) in spite of the known fact that NIV is BSL 4 level pathogen whereas MCVR is a level BSL2+lab. Prior to this training to MCVR, CDC has not consulted national/govt agencies as per norm. Since Nipah is a high risk pathogen with potential for being used as agent of bio-terrorism the samples were to be handled more carefully and tested only in a BSL4.”

While CDC admitted that the training program didn’t have the necessary approval due to some confusion, it maintained that they did not commission the research directly. “The training was done through the Global Health Security Agenda (GHSA) and was aimed at strengthening laboratory systems in India which allowed for detection of Nipah virus.”

Manipal Center of Virus Research collaboration with US CDC
International collaborations of Manipal Center of Virus Research

CDC has partnered with MCVR to carry out illness surveillance across India under the project known as AFI surveillance which tracks mysterious diseases in the government hospitals. The Indian government has now asked both agencies to stop the surveillance project. It also warned CDC to ensure all funding is approved by the government.

In its defence, MCVR denied carrying out any risky virus isolation work at their lab. Dr. Arunkumar, Director of MCVR, said:

“We did not take approval from HMSC. Prior to testing, MCVR inactivated the virus. Inactivation of the virus was carried out in BSL3 facility at MCVR. Once inactivated, the virus cannot spread. Molecular testing was carried at MCVR in its BSL2 facility. No Nipah virus sample was transferred from MCVR to any other lab (except NIV Pune) within and outside the country.”

Investigation on secret research on Bat Hunters

This is not the first time a dangerous research took place in India without keeping the government in loop. Back in February this year, the officials confirmed to that foreign funded researchers were conducting study on bats and bat hunters (humans) in the northeastern state of Nagaland. Bats are known to often carry viruses such as ebola, SARS coronavirus, rabies,etc.

What’s more alarming was that two of the 12 researchers belonged to the Wuhan Institute of Virology’s Department of Emerging Infectious Diseases – the same institute from where COVID-19 outbreak is believed to have originated. The Nagaland study was funded by the United States Department of Defense’s Defense Threat Reduction agency (DTRA).

The results of the study were published in October last year in the PLOS Neglected Tropical Diseases journal, originally established by the Bill and Melinda Gates Foundation.

To conduct a high-risk study in India, they would have needed special permissions from the Indian authorities which was not sought by the parties involved in the study. The fact that scientists from foreign countries were allowed to handle live samples of bats and bat hunters without permission prompted Indian Council of Medical Research (ICMR) to send a five-member committee to investigate the matter.

Funding of controversial Gain-of-Function research

Even before the coronavirus outbreak, a number of controversial studies were being carried out at China’s Wuhan lab under the patronage of United States’ National Institutes of Health (NIH). One of the studies is the gain-of-function research on bat coronaviruses which involves mutating viruses in the lab to explore their potential for infecting humans.

The gain-of-function research has been widely criticized by the scientists around the world due to the risk of starting a pandemic from accidental release.

However, last year the National Institute for Allergy and Infectious Diseases, the organization led by Dr. Anthony Fauci, funded scientists at the Wuhan Institute of Virology and other institutions for work on gain-of-function research. A total of $7.5 million of American tax dollars have been spent since 2014 for conducting GoF studies.

Role of CDC in Surat plague

The plague outbreak in the western Indian city of Surat in 1994 has been mired in controversy just as COVID-19. Around 55 people died and close to a half of the city of 1.2 million people fled Surat for fear of the plague and of being quarantined.

The origin of the outbreak is still a mystery. Indian defense establishment believes the 1994 Surat Plague is a case of bioterrorism. Numerous media outlets at the time reported the involvement of American CDC. It was suspected that the germ with an extra protein ring was developed by a CDC lab in Almaty, Kazakhstan.

Thus it comes as no surprise that Indian authorities are taking no chances this time around with CDC, especially since the world is already under the grip of a virus pandemic and the role of CDC is increasingly being seen as suspicious. >> GGI

Additionally, The Week Magazine from India reported recently:

<< Did the novel coronavirus leak similarly through a worker in a biowar lab in Wuhan? The Washington Times, which is known for its CIA links, has raised the suspicion in an article quoting Dany Shoham, a former Israeli military intelligence officer who has studied Chinese biowarfare.

Indian scientists would not rule out the possibility. The Wuhan lab, said Dr William Selvamurthy, a former chief controller of the Defence Research and Development Organisation who was in charge of the life science labs, could have been keeping the virus under BSL-4 (biosafety level-4)—the most secure condition for reseach. So, the possibility of someone having been infected from the lab and inadvertently spreading it could not be ruled out, said Selvamurthy.

The Wuhan Institute is officially acknowledged to be China’s most advanced virus research lab complex. China, a signatory to the Biological Weapons Convention (BWC) since 1985, had, in 1993, declared the Wuhan Institute of Biological Products as one of eight biowarfare research facilities covered by the BWC. Yet, last year’s US state department report on arms control compliance had accused China of working on military pathogens for offensive purposes. It said the US had concerns with respect to “Chinese military medical institutions’ toxin research and development because of the potential dual-use applications and their potential as a biological threat”.

China has maintained that the virus has originated from wild animals sold at a market in Wuhan. The lab under suspicion is just about 30km from the market. The virus has been identified as a virulent strain, much like any classical germ warfare strain—they were designed to be virulent initially, but quickly controllable. The idea, as a military scientist explained, was for the germ to be released in hostile territory to disable the enemy, but the territory would have to be quickly sanitised for your own forces to capture it.

During the 1994 plague outbreak in Surat and Beed, it was found that the germs had an extra protein ring which could only have been inserted artificially. Indian scientists had raised concerns about a US biowar experiment having gone awry. THE WEEK had carried reports giving details of germ war research being carried on in labs under the Centre for Disease Control in Atlanta and about a newly developed germ detector being tested. The US embassy had denied the allegations. There were also reports that the Surat germ could have been developed in a lab in Almaty, Kazakhstan.

There have been rumours and reports in Chinese cybermedia in the last few days suggesting that the Wuhan outbreak could have been a US biowar attack. This, US officials consider, was an attempt to preempt charges that the new virus had escaped from the Wuhan lab, which had been in the crosshairs of the west especially after a team of Chinese virologists working in a lab in Winnipeg, Canada, unauthorisedly sent samples of some of the deadliest viruses on earth to China.” >> – The Week Mag

To be continued?
Our work and existence, as media and people, is funded solely by our most generous readers and we want to keep this way.
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! Articles can always be subject of later editing as a way of perfecting them

Maybe one day we will beg for masks to protect ourselves from vaccines

MIT article
Our article

To be continued?
Our work and existence, as media and people, is funded solely by our most generous readers and we want to keep this way.
We hardly made it before, but this summer something’s going on, our audience stats show bizarre patterns, we’re severely under estimates and the last savings are gone. We’re not your responsibility, but if you find enough benefits in this work…
Help SILVIEW.media survive and grow, please donate here, anything helps. Thank you!

! Articles can always be subject of later editing as a way of perfecting them

https://youtu.be/BVVdv5Vp0S8