vaccinations

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by Silviu “Silview” Costinescu

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.

FACTCHECK.ORG
SNOPES
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 Law, in 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
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).

SOURCE

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

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by Silviu “Silview” Costinescu

Not the writer, the first man to undertake the Covid gene therapy.

I closed the case in this post’s cover gif animation.
All I have to add is a few references:

SOURCE
Source
SOURCE
SOURCE


“Experimental” means we are not done finding out what relates to it, how and when.

SILVIEW.media

To be continued?
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ORDER

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by Silviu “Silview” Costinescu

Warning: Mathematical estimations might make you sick to your stomach!

UPDATES:
58% of VAERS data is Jan or older! 5/7/2021

As predicted, it only got worse. I have no words to describe how bad… 5/16/2021

MORE COVID JAB REACTIONS THAN COVID CASES IN ER – WE’RE ALREADY THERE! 5/17/2021

SEE MORE

AND THEN IT WENT ON…

At this point we can only rely on these facts:

This is a catastrophe.

This is a coverup.

The ripple-effects will go beyond imagination.

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by Silviu “Silview” Costinescu

Yes, the vaccine passports too, like many other “novel ideas” brought up by the “novel” Macarenavirus, have been actually planned long ago.

DOWNLOAD PDF FROM EUROPEAN COMMISSION WEBSITE

IN OTHER NEWS

24 world leaders announce international pandemic treaty to implement Great Reset agenda

Signatories include the head of the World Health Organization, as well as the leaders of France, Germany, the U.K., and other countries.

FROM EUROPEAN COMMISSION WEBSITE

March 31, 2021 (LifeSiteNews) –– A host of global leaders issued a call for a global pandemic treaty, purportedly in order to prevent future pandemics, distribute vaccinations, and implement a unilateral approach to global governance.

U.K. Prime Minister Boris Johnson, French President Emmanuel Macron, German Chancellor Angela Merkel, the head of the World Health Organisation (WHO), as well as 20 other world leaders, joined forces in penning a joint letter with the apparent intent of winning popular support for the globalist plan.

Writing in U.K. paper The Telegraph, as well as other publications such as Le Monde in France, the leaders declared their intent to “build a more robust international health architecture that will protect future generations.”

Calling COVID-19 the “biggest challenge to the global community since the 1940s,” the 24 leaders predicted that there “will be other pandemics and other major health emergencies.”

“No single government or multilateral agency can address this threat alone,” they declared. “The question is not if, but when. Together, we must be better prepared to predict, prevent, detect, assess and effectively respond to pandemics in a highly co-ordinated fashion. The Covid-19 pandemic has been a stark and painful reminder that nobody is safe until everyone is safe.”

This final phrase could indicate the influence which World Economic Forum (WEF) founder and committed globalist Klaus Schwab enjoys over the 24 leaders. Just weeks ago, Schwab declared, “As long as not everybody is vaccinated, nobody will be safe,” a statement which in itself poses an interesting question about the trust which such leaders are placing in their much praised, but dangerous, experimental injections.

The leaders re-affirmed their joint aim of global vaccination, describing it as “global public good.”

In order to achieve that “public good,” and to ensure swift roll-out of vaccines across the globe, the 24 globalists initiated their new international treaty: “[W]e believe that nations should work together towards a new international treaty for pandemic preparedness and response. Such a renewed collective commitment would be a milestone in stepping up pandemic preparedness at the highest political level.”

This treaty would be based on the principles of the WHO, drawing from the WHO’s constitution, as well as calling on “other relevant organisations key to this endeavour.” The WHO’s director-general, Dr. Tedros Adhanom Ghebreyesus, was one of the signatories of the statement.

“The main goal of this treaty would be to foster an all of government and all of society approach, strengthening national, regional and global capacities and resilience to future pandemics,” the leaders declared.

“This includes greatly enhancing international co-operation to improve, for example, alert systems, data-sharing, research and local, regional and global production and distribution of medical and public health counter-measures such as vaccines, medicines, diagnostics and personal protective equipment.”

Nor would it be centered purely on globalist vaccination agendas. Due to the leaders’ “One Health” approach, it would build on the principle of a connection between “the health of humans, animals and our planet.”

In language reminiscent of the Great Reset agenda, promoted by the WEF and Klaus Schwab, the leaders mentioned that the new treaty would lead to a lack of national interests, and increased international concerns: “[S]uch a treaty should lead to more mutual accountability and shared responsibility, transparency and co-operation within the international system and with its rules and norms.”

No section of society would be exempt from becoming involved in the new treaty, whatever it may turn out to look like, with the world leaders pointing out that “we will work with heads of state and governments globally, and all stakeholders including civil society and the private sector.”

Declaring that the coronavirus, which originated in Wuhan, China, had “exploited our weaknesses and divisions,” the leaders pronounced it to be their “responsibility” to “ensure that the world learns the lessons of the Covid-19 pandemic,” and to “seize this opportunity and come together as a global community for peaceful co-operation that extends beyond this crisis.”

The proposal is due to be further discussed among national leaders at the June G7 summit in Cornwall in the U.K., where Boris Johnson will join his counterparts from Canada, France, Germany, Italy, Japan, the U.S., and the E.U. Meanwhile, the 24 signatories warned that their new plan “will take time and require a sustained political, financial and societal commitment over many years.”

Speaking to BBC Radio, the WHO’s special COVID envoy Dr. David Nabarro, echoed the language employed by the 24 leaders, noting that it would be 2022 before the globalist agenda of world vaccination was complete, and thus hinted at “all sorts of problems with variants,” before that goal was complete.

The planned treaty appears to align very closely with the Great Reset goals of Klaus Schwab. The World Economic Forum’s promotion of the Reset even employs matching terminology, describing “leaders” who “find themselves at a historic crossroads.”

The societal disruption caused by the Wuhan virus presents “a unique window of opportunity to shape the recovery” for Schwab, who added that “this initiative will offer insights to help inform all those determining the future state of global relations, the direction of national economies, the priorities of societies, the nature of business models and the management of a global commons.”

Indeed, the link between the new international treaty and the Great Reset caused veteran presenter Richie Allen to write, “This is terrifying. For many years, I have been featuring writers, researchers and academics who warned us that this would happen. This is the end game.”

Such a treaty was simply about “concentrating power in the hands of a tiny elite,” explained Allen. “It’s what globalists have been working towards for decades.”

The full list of signatories is found below:

J. V. Bainimarama, prime minister of Fiji; António Luís Santos da Costa, prime minister of Portugal; Klaus Iohannis, president of Romania; Boris Johnson, prime minister of the United Kingdom; Paul Kagame, president of Rwanda; Uhuru Kenyatta, president of Kenya; Emmanuel Macron, president of France; Angela Merkel, chancellor of Germany; Charles Michel, president of the European Council; Kyriakos Mitsotakis, prime minister of Greece; Moon Jae-in, president of the Republic of Korea; Sebastián Piñera, president of Chile; Carlos Alvarado Quesada, president of Costa Rica; Edi Rama, prime minister of Albania; Cyril Ramaphosa, president of South Africa; Keith Rowley, prime minister of Trinidad and Tobago; Mark Rutte, prime minister of the Netherlands; Kais Saied, president of Tunisia; Macky Sall, president of Senegal; Pedro Sánchez, Prime Minister of Spain; Erna Solberg, prime minister of Norway; Aleksandar Vučić, president of Serbia; Joko Widodo, president of Indonesia; Volodymyr Zelensky, president of Ukraine; Dr. Tedros Adhanom Ghebreyesus, director-general of the World Health Organisation.

To be continued?
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We think frequent mask use, even short term use can be bad for you, but if you have no way around them, at least send a message of consciousness.
Get it here!

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by Silviu “Silview” Costinescu

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

MIT article
Our article

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by Silviu “Silview” Costinescu

I don’t know if they do it, because no independent researchers examine those swabs, but I have always pointed out that our overlords seem more concerned with testing than with vaccinating. Almost like the vaccines were the bait and tests were the switch. And now we also know they totally CAN do that.
Just follow the science below.

The respectable Mr. David Knight makes a summary of our article

UPDATE: LMAO, THIS WENT SO VIRAL VICE WAS SENT TO DEBUNK IT, SEE FOR YOURSELF, IT’S HILARIOUS!

Our comment has already been deleted, apparently, or I can’t find it anymore 😀
Attn: Gates-paid fact-checkers – Injectable computers with RFID antennas produced in 2016

UPDATE: DR. LORRAINE DAY QUOTES AND FURTHER EXPLAINS THIS VERY ARTICLE!

Share the video in higher resolution from our Bitchute or Lbry

November 3, 2020

Researchers engineer tiny machines that deliver medicine efficiently

by Johns Hopkins University School of Medicine

Johns Hopkins Researchers engineer tiny machines that deliver medicine efficiently
A theragripper is about the size of a speck of dust. This swab contains dozens of the tiny devices. Credit: Johns Hopkins University.

Inspired by a parasitic worm that digs its sharp teeth into its host’s intestines, Johns Hopkins researchers have designed tiny, star-shaped microdevices that can latch onto intestinal mucosa and release drugs into the body.

David Gracias, Ph.D., a professor in the Johns Hopkins University Whiting School of Engineering, and Johns Hopkins gastroenterologist Florin M. Selaru, M.D., director of the Johns Hopkins Inflammatory Bowel Disease Center, led a team of researchers and biomedical engineers that designed and tested shape-changing microdevices that mimic the way the parasitic hookworm affixes itself to an organism’s intestines.

Made of metal and thin, shape-changing film and coated in a heat-sensitive paraffin wax, “theragrippers,” each roughly the size of a dust speck, potentially can carry any drug and release it gradually into the body.

The team published results of an animal study this week as the cover article in the journal Science Advances.

Gradual or extended release of a drug is a long-sought goal in medicine. Selaru explains that a problem with extended-release drugs is they often make their way entirely through the gastrointestinal tract before they’ve finished dispensing their medication.

“Normal constriction and relaxation of GI tract muscles make it impossible for extended-release drugs to stay in the intestine long enough for the patient to receive the full dose,” says Selaru, who has collaborated with Gracias for more than 10 years. “We’ve been working to solve this problem by designing these small drug carriers that can autonomously latch onto the intestinal mucosa and keep the drug load inside the GI tract for a desired duration of time.”

Researchers engineer tiny machines that deliver medicine efficiently
When an open theragripper, left, is exposed to internal body temperatures, it closes on the instestinal wall. In the gripper’s center is a space for a small dose of a drug. Credit: Johns Hopkins University

Thousands of theragrippers can be deployed in the GI tract. When the paraffin wax coating on the grippers reaches the temperature inside the body, the devices close autonomously and clamp onto the colonic wall. The closing action causes the tiny, six-pointed devices to dig into the mucosa and remain attached to the colon, where they are retained and release their medicine payloads gradually into the body. Eventually, the theragrippers lose their hold on the tissue and are cleared from the intestine via normal gastrointestinal muscular function.

Taken from the original research annexes

Gracias notes advances in the field of biomedical engineering in recent years.

“We have seen the introduction of dynamic, microfabricated smart devices that can be controlled by electrical or chemical signals,” he says. “But these grippers are so small that batteries, antennas and other components will not fit on them.”

Theragrippers, says Gracias, don’t rely on electricity, wireless signals or external controls. “Instead, they operate like small, compressed springs with a temperature-triggered coating on the devices that releases the stored energy autonomously at body temperature.”

The Johns Hopkins researchers fabricated the devices with about 6,000 theragrippers per 3-inch silicon wafer. In their animal experiments, they loaded a pain-relieving drug onto the grippers. The researchers’ studies found that the animals into which theragrippers were administered had higher concentrates of the pain reliever in their bloodstreams than did the control group. The drug stayed in the test subjects’ systems for nearly 12 hours versus two hours in the control group.

“You could put the computational power of the spaceship Voyager onto an object the size of a cell”. In 2018.
“Swarms of microscopic robots that can be injected”
Tell Melinda Gates we can inject robots and computers these days.

At this point I just need to recall our October 2020 article: FACT-CHECKERS LIE: TEST SWABS REALLY LIKELY TO GIVE YOU THE “LEAKY BRAIN”

HERE’S A VERY SIMPLE WAY TO ATTACK THE BRAIN THROUGH THE TEST SWABS

I’ve seen a report on someone who had to undergo tests almost daily and he developed brain cancer over the course of about three months. But I can’t verify it, so that’s all it’s worth.

SPOOKY FIBERS IN MAKS AND TEST SWABS? WAIT ’TIL YOU READ THE SCIENCE!

SOURCE

Aaaand the last piece of the puzzle that we needed to get the picture. We may have missed many details, but we got the core idea right:

SOURCE

“Key to our findings is the demonstration that S1 promotes loss of barrier integrity in an advanced 3D microfluidic model of the human BBB, a platform that more closely resembles the physiological conditions at this CNS interface. Evidence provided suggests that the SARS-CoV-2 spike proteins trigger a pro-inflammatory response on brain endothelial cells that may contribute to an altered state of BBB function. Together, these results are the first to show the direct impact that the SARS-CoV-2 spike protein could have on brain endothelial cells; thereby offering a plausible explanation for the neurological consequences seen in COVID-19 patients.”

Report contents include:

  • Market analysis of nano-based diagnostic tests for COVID-19 including nanosensors incorporating gold nanoparticles, iron oxide nanoparticles, graphene, quantum dots, carbon quantum dots and carbon nanotubes. Market revenues adjusted to pandemic outcomes. In-depth company profiles. Companies profiled include Abbott Laboratories, Cardea, Ferrotec (USA) Corporation, E25Bio, Grolltex, Inc., Luminex Corporation etc.

More info here: A DIVERSITY OF NANOTECH 100% CONFIRMED IN COVID TESTS, MASKS, INJECTIONS AND A WIDE RANGE OF PRODUCTS

Application of Nanotechnology in the COVID-19 Pandemic

Dongki Yang1

Internationa Journal of Nanomedicine. 2021; 16: 623–649.
Published online 2021 Jan 26. 
doi: 10.2147/IJN.S296383

Intranasal Delivery Therapy

Currently, many studies are being conducted on developing a method for delivering nanoparticles into the nasal cavity as a safe and more effective countermeasure against viral infection and treatment.180 Since SARS-CoV-2 initiates infection on the mucosal surface of the eye or nasal cavity, mucosal therapy is the most important strategy for treating such infectious diseases. Delivery through the nasal cavity is not only simple and inexpensive but also non-invasive, and the NP is rapidly absorbed due to the cavity’s abundant capillary plexus and large surface area.181 The properties of the NPs, such as the surface charge, size, and shape, are important factors to be considered while optimizing the method of delivery to the nasal cavity and play a critical role in effective and safe treatment.182 Studies have been conducted using small animals to evaluate the system that is delivered to the lungs by administering NPs to the nasal cavity. Therefore, findings of these animal studies cannot be easily generalized to humans. To date, three types of NPs (organic, inorganic, and virus-like NPs) have been designed with delivery capabilities that are suitable for therapeutic purposes, which can also be administered intranasally for effective delivery.

Nasal-nanotechnology: revolution for efficient therapeutics delivery

Amrish Kumar 1, Aditya Nath Pandey 1, Sunil Kumar Jain 1

Drug Delivery 2016;  Epub 2014 Jun 5.

Abstract

Context: In recent years, nanotechnology-based delivery systems have gained interest to overcome the problems of restricted absorption of therapeutic agents from the nasal cavity, depending upon the physicochemical properties of the drug and physiological properties of the human nose.

Objective: The well-tolerated and non-invasive nasal drug delivery when combined with the nanotechnology-based novel formulations and carriers, opens the way for the effective systemic and brain targeting delivery of various therapeutic agents. To accomplish competent drug delivery, it is imperative to recognize the interactions among the nanomaterials and the nasal biological environment, targeting cell-surface receptors, drug release, multiple drug administration, stability of therapeutic agents and molecular mechanisms of cell signaling involved in patho-biology of the disease under consideration.

Methods: Quite a few systems have been successfully formulated using nanomaterials for intranasal (IN) delivery. Carbon nanotubes (CNTs), chitosan, polylactic-co-glycolic acid (PLGA) and PLGA-based nanosystems have also been studied in vitro and in vivo for the delivery of several therapeutic agents which shown promising concentrations in the brain after nasal administration.

Results and conclusion: The use of nanomaterials including peptide-based nanotubes and nanogels (NGs) for vaccine delivery via nasal route is a new approach to control the disease progression. In this review, the recent developments in nanotechnology utilized for nasal drug delivery have been discussed.

Keywords: Intranasal; nano-delivery systems; nasal vaccination; non-invasive; nose-to-brain delivery.

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Inhaled nanoparticles–a current review

Wei Yang 1, Jay I Peters, Robert O Williams 3rd

International Journal of Pharmaceutics 2008 May 22;

Abstract

The field of nanotechnology may hold the promise of significant improvements in the health and well being of patients, as well as in manufacturing technologies. The knowledge of this impact of nanomaterials on public health is limited so far. This paper briefly reviews the unique size-controlled properties of nanomaterials, their disposition in the body after inhalation, and the factors influencing the fate of inhaled nanomaterials. The physiology of the lung makes it an ideal target organ for non-invasive local and systemic drug delivery, especially for protein and poorly water-soluble drugs that have low oral bioavailability via oral administration. The potential application of pulmonary drug delivery of nanoparticles to the lungs, specifically in context of published results reported on nanomaterials in environmental epidemiology and toxicology is reviewed in this paper.


Nanoparticles for nasal vaccination

Noemi Csaba 1, Marcos Garcia-Fuentes, Maria Jose Alonso

Advanced Drug Delivery Review. 
2009 Feb 27; doi: 10.1016/j.addr.2008.09.005. Epub 2008 Dec 13.

Abstract

The great interest in mucosal vaccine delivery arises from the fact that mucosal surfaces represent the major site of entry for many pathogens. Among other mucosal sites, nasal delivery is especially attractive for immunization, as the nasal epithelium is characterized by relatively high permeability, low enzymatic activity and by the presence of an important number of immunocompetent cells. In addition to these advantageous characteristics, the nasal route could offer simplified and more cost-effective protocols for vaccination with improved patient compliance. The use of nanocarriers provides a suitable way for the nasal delivery of antigenic molecules. Besides improved protection and facilitated transport of the antigen, nanoparticulate delivery systems could also provide more effective antigen recognition by immune cells. These represent key factors in the optimal processing and presentation of the antigen, and therefore in the subsequent development of a suitable immune response. In this sense, the design of optimized vaccine nanocarriers offers a promising way for nasal mucosal vaccination.

Similar articles

Check the follow ups in the Bio-hacking trilogy:

RNA MODIFICATION USED TO ALTER DNA, BRAIN FUNCTIONS AND BEHAVIOR
Part 3 went straight to video:
THE WALKING SERVERS. DON’T BE ONE, LEARN ABOUT DNA STORAGE, DNA PRIVACY AND BIOHACKING – DOCUMENTARY

Epub 2008 Dec 13.

Nanoparticles for nasal vaccination

Noemi Csaba  1 , Marcos Garcia-Fuentes, Maria Jose Alonso

Abstract

The great interest in mucosal vaccine delivery arises from the fact that mucosal surfaces represent the major site of entry for many pathogens. Among other mucosal sites, nasal delivery is especially attractive for immunization, as the nasal epithelium is characterized by relatively high permeability, low enzymatic activity and by the presence of an important number of immunocompetent cells. In addition to these advantageous characteristics, the nasal route could offer simplified and more cost-effective protocols for vaccination with improved patient compliance. The use of nanocarriers provides a suitable way for the nasal delivery of antigenic molecules. Besides improved protection and facilitated transport of the antigen, nanoparticulate delivery systems could also provide more effective antigen recognition by immune cells. These represent key factors in the optimal processing and presentation of the antigen, and therefore in the subsequent development of a suitable immune response. In this sense, the design of optimized vaccine nanocarriers offers a promising way for nasal mucosal vaccination.

Similar articles

2015 called…

PubMed, 2015 Jun 9.:

Nanoneurotherapeutics approach intended for direct nose to brain delivery

Shadab Md  1 , Gulam Mustafa  2   3 , Sanjula Baboota  3 , Javed Ali  3 Affiliations Expand

Abstract

Context: Brain disorders remain the world’s leading cause of disability, and account for more hospitalizations and prolonged care than almost all other diseases combined. The majority of drugs, proteins and peptides do not readily permeate into brain due to the presence of the blood-brain barrier (BBB), thus impeding treatment of these conditions.

Objective: Attention has turned to developing novel and effective delivery systems to provide good bioavailability in the brain.

Methods: Intranasal administration is a non-invasive method of drug delivery that may bypass the BBB, allowing therapeutic substances direct access to the brain. However, intranasal administration produces quite low drug concentrations in the brain due limited nasal mucosal permeability and the harsh nasal cavity environment. Pre-clinical studies using encapsulation of drugs in nanoparticulate systems improved the nose to brain targeting and bioavailability in brain. However, the toxic effects of nanoparticles on brain function are unknown.

Result and conclusion: This review highlights the understanding of several brain diseases and the important pathophysiological mechanisms involved. The review discusses the role of nanotherapeutics in treating brain disorders via nose to brain delivery, the mechanisms of drug absorption across nasal mucosa to the brain, strategies to overcome the blood brain barrier, nanoformulation strategies for enhanced brain targeting via nasal route and neurotoxicity issues of nanoparticles.

CLICK

Epub 2013 Oct 16.

Nanoemulsion-based intranasal drug delivery system of saquinavir mesylate for brain targeting

Hitendra S Mahajan  1 , Milind S Mahajan, Pankaj P Nerkar, Anshuman Agrawal Affiliations Expand

Abstract

The central nervous system (CNS) is an immunological privileged sanctuary site-providing reservoir for HIV-1 virus. Current anti-HIV drugs, although effective in reducing plasma viral levels, cannot eradicate the virus completely from the body. The low permeability of anti-HIV drugs across the blood-brain barrier (BBB) leads to insufficient delivery. Therefore, developing a novel approaches enhancing the CNS delivery of anti-HIV drugs are required for the treatment of neuro-AIDS. The aim of this study was to develop intranasal nanoemulsion (NE) for enhanced bioavailability and CNS targeting of saquinavir mesylate (SQVM). SQVM is a protease inhibitor which is a poorly soluble drug widely used as antiretroviral drug, with oral bioavailability is about 4%. The spontaneous emulsification method was used to prepare drug-loaded o/w nanoemulsion, which was characterized by droplet size, zeta potential, pH, drug content. Moreover, ex-vivo permeation studies were performed using sheep nasal mucosa. The optimized NE showed a significant increase in drug permeation rate compared to the plain drug suspension (PDS). Cilia toxicity study on sheep nasal mucosa showed no significant adverse effect of SQVM-loaded NE. Results of in vivo biodistribution studies show higher drug concentration in brain after intranasal administration of NE than intravenous delivered PDS. The higher percentage of drug targeting efficiency (% DTE) and nose-to-brain drug direct transport percentage (% DTP) for optimized NE indicated effective CNS targeting of SQVM via intranasal route. Gamma scintigraphy imaging of the rat brain conclusively demonstrated transport of drug in the CNS at larger extent after intranasal administration as NE.

Similar articles

PubMed Epub, 2016 Jun 28:

Hydrogel nanoparticles and nanocomposites for nasal drug/vaccine delivery

Sara Salatin  1   2 , Jaleh Barar  1   3 , Mohammad Barzegar-Jalali  3 , Khosro Adibkia  3   4 , Mitra Alami Milani  2   4 , Mitra Jelvehgari  5   6 Affiliations Expand

Affiliations

  • 1 Research Center for Pharmaceutical Nanotechnology, Tabriz University of Medical Science, Tabriz, Iran.
  • 2 Student Research Committee, Tabriz University of Medical Science, Tabriz, Iran.
  • 3 Department of Pharmaceutics, Faculty of Pharmacy, Tabriz University of Medical Sciences, Mailbox 51664, Tabriz, Iran.
  • 4 Drug Applied Research Center and Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.
  • 5 Department of Pharmaceutics, Faculty of Pharmacy, Tabriz University of Medical Sciences, Mailbox 51664, Tabriz, Iran. mitra_jelvehgari@yahoo.com.
  • 6 Drug Applied Research Center and Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran. mitra_jelvehgari@yahoo.com.

Abstract

Over the past few years, nasal drug delivery has attracted more and more attentions, and been recognized as the most promising alternative route for the systemic medication of drugs limited to intravenous administration. Many experiments in animal models have shown that nanoscale carriers have the ability to enhance the nasal delivery of peptide/protein drugs and vaccines compared to the conventional drug solution formulations. However, the rapid mucociliary clearance of the drug-loaded nanoparticles can cause a reduction in bioavailability percentage after intranasal administration. Thus, research efforts have considerably been directed towards the development of hydrogel nanosystems which have mucoadhesive properties in order to maximize the residence time, and hence increase the period of contact with the nasal mucosa and enhance the drug absorption. It is most certain that the high viscosity of hydrogel-based nanosystems can efficiently offer this mucoadhesive property. This update review discusses the possible benefits of using hydrogel polymer-based nanoparticles and hydrogel nanocomposites for drug/vaccine delivery through the intranasal administration.

Keywords: Brain; Hydrogel; Nanoparticles; Nasal delivery; Vaccine.

Similar articles

To be continued?
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UK’s Government’s Medicines & Healthcare products Regulatory Agency (MHRA) spends close to $2million on an Artificial Intelligence to monitor “Medicines & Healthcare products Regulatory Agency”. If this isn’t alarming, I don’t know what is. But I know there’s more to the story.

The MHRA urgently seeks an Artificial Intelligence (AI) software tool to process the expected high volume of Covid-19 vaccine Adverse Drug Reaction (ADRs) and ensure that no details from the ADRs’ reaction text are missed.

MRHA
DOWNLOAD PDF

Thanks Graham Pick for the tip!

The acquisition document further provides this explanation:

“For reasons of extreme urgency under Regulation 32(2)(c) related to the release of a Covid-19 vaccine MHRA have accelerated the sourcing and implementation of a vaccine specific AI tool.

Strictly necessary — it is not possible to retrofit the MHRA’s legacy systems to handle the volume of ADRs that will be generated by a Covid-19 vaccine. Therefore, if the MHRA does not implement the AI tool, it will be unable to process these ADRs effectively. This will hinder its ability to rapidly identify any potential safety issues with the Covid-19 vaccine and represents a direct threat to patient life and public health.

Reasons of extreme urgency — the MHRA recognises that its planned procurement process for the SafetyConnect programme, including the AI tool, would not have concluded by vaccine launch. Leading to a inability to effectively monitor adverse reactions to a Covid-19 vaccine.

Events unforeseeable — the Covid-19 crisis is novel and developments in the search of a Covid-19 vaccine have not followed any predictable pattern so far.”

Beneficiary of this contract is a company named Genpact, part of a larger multi-industry group with the same name.
Genpact also does Facebook moderation, which gives it access to Facebook data!

Source

Genpact CEO is close to our old friends from WEF, of course

Here he supports using military to distribute the vaccine that will then provide work for his company:

He seems to applaud a Biden victory in the US presidentials. :

This Tyger dude basically has all the traits and inclinations of the elite mafia that set up Covidiocracy as the new business and live-stock management model for the whole world.

Source

Genpact has acquired 23 companies, including 10 in the last 5 years. A total of 8 acquisitions came from private equity firms. Genpact’s largest acquisition to date was in 2011, when it acquired Headstrong for $550M. Genpact has acquired in 11 different US states, and 5 countries. The Company’s most targeted sectors include information technology (28%) and software (28%). – Mergr

Gentec CEO interview

To be continued?
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by Silviu “Silview” Costinescu

One of the most maleficent characters in Trump’s menagerie is this psychopath he named as leader of Operation Warp Speed, Moncef Slaoui, former GSK and Moderna boss having a bigger body count than the Spanish Flu. Actually Kushner picked him in Trumps name, but anyway, after we wrote extensive viral exposes on his past, a team of “specialists” brushed up his online presence and then he laid low for a while. But his silence is over and his newest interviews confirm everything we’ve wrote about him and Covid-19.

For the best understanding of this article, you have to read it as a follow up to four previous pieces that are anyway essential readings:

TRUMP’S NEW MOROCCAN “VACCINE CZAR”: WORKED FOR BILL GATES, GOOGLE, GSK. WORKED IN CHINA. TRANSHUMANIST. LOCKDOWN FANATIC

CORRUPTION UNLTD: GSK AND “TRUMP’S VACCINE CZAR”. SEX TAPES, DEAD BABIES, BRIBES AND PROSTITUTES

EXCLUSIVE: GATES, FAUCI AND SLAOUI HAVE LONG BEEN COOKING AND SELLING SCANDALOUS VACCINES TOGETHER. IT’S A CARTEL

IT’S NOT 5G AND COVID-19, IT’S DATA AND VACCINATIONS. US AND CHINA HAVE LONG USED WHO AS PLATFORM TO COLLABORATE ON THIS

“If you take the first Operation Warp Speed vaccine  you will get an unexpected surprise: micromanaged tracking by Big Tech for up to two years, who will know more about you than you know about yourself. There is no guarantee that tracking will stop after two years.” writes Technocracy News

” It should become apparent that the military/industrial complex that is running Warp Speed is functionally merged with Big Tech like Google and Oracle. And then, there is the federal government itself that is driving the entire vaccination program”, adds TN and they’re not wrong.

Moncef Slaoui, the official head of Operation Warp Speed, told the Wall Street Journal last week that all Warp Speed vaccine recipients in the US will be monitored by “incredibly precise . . . tracking systems” for up to two years and that tech giants Google and Oracle would be involved.

Another high from Slaoui’s career that looks more like a bloodbath.

Last week, a rare media interview given by the Trump administration’s “Vaccine Czar” offered a brief glimpse into the inner workings of the extremely secretive Operation Warp Speed (OWS), the Trump administration’s “public-private partnership” for delivering a Covid-19 vaccine to 300 million Americans by next January. What was revealed should deeply unsettle all Americans.

During an interview with the Wall Street Journal published last Friday, the “captain” of Operation Warp Speed, career Big Pharma executive Moncef Slaoui, confirmed that the millions of Americans who are set to receive the project’s Covid-19 vaccine will be monitored via “incredibly precise . . . tracking systems” that will “ensure that patients each get two doses of the same vaccine and to monitor them for adverse health effects.” Slaoui also noted that tech giants Google and Oracle have been contracted as part of this “tracking system” but did not specify their exact roles beyond helping to “collect and track vaccine data.”

The day before the Wall Street Journal interview was published, the New York Times published a separate interview with Slaoui where he referred to this “tracking system” as a “very active pharmacovigilance surveillance system.” During a previous interview with the journal Science in early September, Slaoui had referred to this system only as “a very active pharmacovigilance system” that would “make sure that when the vaccines are introduced that we’ll absolutely continue to assess their safety.” Slaoui has only recently tacked on the words “tracking” and “surveillance” to his description of this system during his relatively rare media interviews.

While Slaoui himself was short on specifics regarding this “pharmacovigilance surveillance system,” the few official documents from Operation Warp Speed that have been publicly released offer some details about what this system may look like and how long it is expected to “track” the vital signs and whereabouts of Americans who receive a Warp Speed vaccine.

This is basically what we meant by “It’s about data and vaccines” in our headline above. And 5G will follow Covid around because all this data needs carried by a medium and many antennas. Which, while doing their work, can also produce Covid-like symptoms, as a bonus benefit for the Covidiocracy orchestrators.

Stuff that no one mentions in Slaoui’s romanced biographies

The Last American Vagabond takes it from here into finer details in one of his latest posts, demonstrating we’re guinea pigs and this is how they will study us:

The Pharmacovigilantes

Two official OWS documents released in mid-September state that vaccine recipients—expected to include a majority of the US population—would be monitored for twenty-four months after the first dose of a Covid-19 vaccine is administered and that this would be done by a “pharmacovigilance system.”

In the OWS document entitled “From the Factory to the Frontlines,” the Department of Health and Human Services (HHS) and the Department of Defense (DOD) stated that, because Warp Speed vaccine candidates use new unlicensed vaccine production methods that “have limited previous data on safety in humans . . . the long-term safety of these vaccines will be carefully assessed using pharmacovigilance surveillance and Phase 4 (post-licensure) clinical trials.”

It continues:

The key objective of pharmacovigilance is to determine each vaccine’s performance in real-life scenarios, to study efficacy, and to discover any infrequent and rare side effects not identified in clinical trials. OWS will also use pharmacovigilance analytics, which serves as one of the instruments for the continuous monitoring of pharmacovigilance data. Robust analytical tools will be used to leverage large amounts of data and the benefits of using such data across the value chain, including regulatory obligations.

In addition, Moncef Slaoui and OWS’s vaccine coordinator, Matt Hepburn, formerly a program manager at the Pentagon’s controversial Defense Advanced Research Projects Agency (DARPA), had previously published an article in the New England Journal of Medicine that stated that “because some technologies have limited previous data on safety in humans, the long-term safety of these vaccines will be carefully assessed using pharmacovigilance surveillance strategies.”

The use of pharmacovigilance on those who receive the vaccine is also mentioned in the official Warp Speed “infographic,” which states that monitoring will be done in cooperation with the Food and Drug Administration (FDA) and the Centers for Disease Control and Protection (CDC) and will involve “24 month post-trial monitoring for adverse effects.”

In a separate part of that same document, OWS describes one of its “four key tenets” as “traceability,” which has three goals: to “confirm which of the approved vaccines were administered regardless of location (private/public)”; to send a “reminder to return for second dose”; and to “administer the correct second dose.”

Regarding a Covid-19 vaccine requiring more than one dose, a CDC document associated with Operation Warp Speed states:

For most Covid-19 vaccine products, two doses of vaccine, separated by 21 or 28 days, will be needed. Because different Covid-19 vaccine products will not be interchangeable, a vaccine recipient’s second dose must be from the same manufacturer as their first dose. Second-dose reminders for vaccine recipients will be critical to ensure compliance with vaccine dosing intervals and achieve optimal vaccine effectiveness.

The CDC document also references a document published in August by the Johns Hopkins Center for Health Security, associated with the Event 201 and Dark Winter simulations, as informing its Covid-19 vaccination strategy. The Johns Hopkins paper, which counts Dark Winter co-organizer Thomas Inglesby as one of its authors, argues that existing “passive reporting” systems managed by the CDC and FDA should be retooled to create “an active safety surveillance system directed by the CDC that monitors all [Covid-19] vaccine recipients—perhaps by short message service or other electronic mechanisms.”

Despite the claims in these documents that the “pharmacovigilance surveillance system” would intimately involve the FDA, top FDA officials stated in September that they were barred from attending OWS meetings and told reporters they could not explain the operation’s organization or when or with what frequency its leadership meets. The FDA officials did state, however, that they “are still allowed to interact with companies developing products for OWS,” STAT news reported.

In addition, the FDA has apparently “set up a firewall between the vast majority of staff and the initiative [Operation Warp Speed]” that appears to drastically limit the number of FDA officials with any knowledge of or involvement in Warp Speed. The FDA’s director of the Center for Drug Evaluation and Research, Janet Woodcock, is the only FDA official listed as having any direct involvement in OWS and appears to be personally managing this “firewall” at the FDA. Woodcock describes herself as a long-time advocate for the use of “big data” in the evaluation of drug and vaccine safety and has been intimately involved in FDA precursors to the coming Warp Speed “pharmacovigilance surveillance system” known as Sentinel and PRISM, both of which are discussed later in this report.

Woodcock is currently on a temporary leave of absence from her role as the director of the Center for Drug Evaluation and Research, which allows her to focus her complete attention on overseeing aspects of Operation Warp Speed on behalf of the FDA’s Office of the Commissioner. Her temporary replacement at the FDA, Patrizia Cavazzoni, is “very aligned with Janet and where the agency is going,” according to media reports. Cavazzoni is a former executive at Pfizer, one of the companies producing a vaccine for OWS. That vaccine is set to begin testing in children as young as 12 years old.

The extreme secrecy of Operation Warp Speed has affected not only the FDA but also the CDC, as a CDC expert panel normally involved in developing the government’s vaccine distribution strategies was “stonewalled” by Matt Hepburn, OWS’s vaccine coordinator, who bluntly refused to answer several of the panel’s “pointed questions” about the highly secretive operation.

More Secret Contracts

While Moncef Slaoui and Warp Speed documents provide few details regarding what this “tracking system” would entail, Slaoui did note in his recent interview with the Wall Street Journal that tech giants Google and Oracle had been contracted to “collect and track vaccine data” as part of this system. Neither Google nor Oracle, however, has announced receipt of a contract related to Operation Warp Speed, and the DOD and HHS, similarly, have yet to announce the awarding of any Warp Speed contract to either Google or Oracle. In addition, searches on the US government’s Federal Register and on the official website for federally awarded contracts came up empty for any contract awarded to Google or Oracle that would apply to any such “pharmacovigilance” system or any other aspect of Operation Warp Speed.

Given my previous reporting on the use of a nongovernment intermediary for awarding OWS contracts to vaccine companies, it seems likely that Warp Speed contracts awarded to Google and Oracle were made using a similar mechanism. In an October 6, 2020, report for The Last American Vagabond, I noted that $6 billion in Warp Speed contracts awarded to vaccine companies were made through Advanced Technology International (ATI), a government contractor that works mainly with the military and surveillance technology companies and whose parent company has strong ties to the CIA and the 2001 Dark Winter simulation. HHS, which is supposedly overseeing Operation Warp Speed, claimed to have “no record” of at least one of those contracts. Only one Warp Speed vaccine contract, which did not involve ATI and was awarded directly by HHS’s Biomedical Advanced Research and Development Authority, was recently obtained by KEI Online. Major parts of the contract, however, including the section on intellectual property rights, were redacted in their entirety.

If the Warp Speed contracts that have been awarded to Google and Oracle are anything like the Warp Speed contracts awarded to most of its participating vaccine companies, then those contracts grant those companies diminished federal oversight and exemptions from federal laws and regulations designed to protect taxpayer interests in the pursuit of the work stipulated in the contract. It also makes them essentially immune to Freedom of Information Act (FOIA) requests. Yet, in contrast to the unacknowledged Google and Oracle contracts, vaccine companies have publicly disclosed that they received OWS contracts, just not the terms or details of those contracts. This suggests that the Google and Oracle contracts are even more secretive.

A major conflict of interest worth noting is Google’s ownership of YouTube, which recently banned on its massive multimedia platform all “misinformation” related to concerns about a future Covid-19 vaccine. With Google now formally part of Operation Warp Speed, it seems likely that any concerns about OWS’s extreme secrecy and the conflicts of interest of many of its members (particularly Moncef Slaoui and Matt Hepburn) as well as any concerns about Warp Speed vaccine safety, allocation and/or distribution may be labeled “Covid-19 vaccine misinformation” and removed from YouTube.

From the NSA to the FDA: The New PRISM

Though the nature of this coming surveillance system for Covid-19 vaccine recipients has yet to be fully detailed by Warp Speed or the tech companies the operation has contracted, OWS documents and existing infrastructure at the FDA offer a clue as to what this system could entail.

For instance, the Warp Speed document “From the Factory to the Frontlines” notes that the pharmacovigilance system will be a new system created exclusively for OWS that will be “buil[t] off of existing IT [information technology] infrastructure” and will fill any “gaps with new IT solutions.” It then notes that “the Covid-19 vaccination program requires significant enhancement of the IT that will support enhancements and data exchange that are critical for a multi-dose candidate to ensure proper administration of a potential second dose.” The document also states that all data related to the OWS vaccine distribution effort “will be reported into a common IT infrastructure that will support analysis and reporting,” adding that this “IT infrastructure will support partners with a broad range of tools for record-keeping, data on who is being vaccinated, and reminders for second doses.”

Though some Warp Speed documents hint as to the existing IT systems that will serve as the foundation for this new tracking system, arguably the most likely candidate is the FDA-managed Sentinel Initiative, which was established in 2009 during the H1N1 Swine flu pandemic. Like Operation Warp Speed itself, Sentinel is a public-private partnership and involves the FDA, private business, and academia.

According to its website, Sentinel’s “main goal is to improve how FDA evaluates the safety and performance of medical products” through big data, with an additional focus on “learning more about potential side effects.” Media reports describe Sentinel as “an electronic surveillance system that aggregates data from electronic medical records, claims and registries that voluntarily participate and allows the agency to track the safety of marketed drugs, biologics and medical devices.”

One of Sentinel’s main proponent at the FDA is Janet Woodcock, who has aggressively worked to expand the program as director of the FDA’s Center for Drug Evaluation and Research, with a focus on Sentinel’s use in “post-market effectiveness studies.” As previously mentioned, Woodcock is the only FDA official listed among the ninety or so “leaders” of OWS, most of whom are part of the US military and lack any health-care or vaccine-production experience.

Woodcock’s temporary replacement at the FDA, Patrizia Cavazzoni, is also very active in efforts to expand Sentinel. STAT news reported earlier this year that Cavazzoni previously “served on the sterling committee of I-MEDS, an FDA-industry partnership which allows drug makers to pay for use of the FDA’s real-world data system known as Sentinel to complete certain safety studies more quickly.”

Sentinel has a series of “collaborating partners” that “provide healthcare data and scientific, technical, and organizational expertise” to the initiative. These collaborating partners include intelligence contractor Booz Allen Hamilton, tech giant IBM, and major US health insurance companies such as Aetna and Blue Cross Blue Shield, among many others. In addition, Sentinel’s Innovation Center, which it describes as the program’s “test bed to identify, develop, and evaluate innovative methods,” is partnered with Amazon, General Dynamics, and Microsoft. Sentinel also has a Community Building and Outreach Center, which is managed by Deloitte consulting, one of the largest consultancy firms in the world that is known for seeking to fill its ranks with former CIA officials.

The Sentinel system’s specific surveillance program aimed at monitoring vaccine effectiveness is known as the Post-licensure Rapid Immunization Safety Monitoring Program, better known as PRISM. Sentinel’s PRISM was “developed to monitor vaccine safety, but [to date] has never been used to assess vaccine effectiveness.” PRISM was initially launched alongside the Sentinel Initiative itself in 2009 “in response to the need to monitor the safety of the H1N1 influenza vaccine” after it was licensed, marketed, and administered. Yet, as previously mentioned, PRISM has yet to be used to assess the effectiveness of any vaccine while quietly expanding for nearly a decade, which implies that the stakeholders in the Sentinel Initiative have a plan to implement this “safety surveillance system” at some point.

The name PRISM may remind readers of the National Security Agency (NSA) program of the same name that became well known throughout the United States following the Edward Snowden revelations. Given this association, it is worth noting that the NSA, as well as the Department of Homeland Security (DHS), are now officially part of Operation Warp Speed and appear to be playing a role in the development of Warp Speed’s “pharmacovigilance surveillance system.” The addition of the NSA and the DHS to the initiative, of course, greatly increases the involvement of US intelligence agencies in the operation, which itself is “dominated” by the military and sorely lacking in civilian public health officials.

CyberScoop first reported in early September that members of the NSA’s Cybersecurity Directorate were involved in Operation Warp Speed, with their role—as well as that of DHS—being framed mainly as offering “cybersecurity advice” to the initiative. However, the NSA and DHS are also offering “guidance” and “services” to both the other federal agencies involved in Warp Speed as well as OWS contractors, which now include Google and Oracle.

Google is well known for its cozy relationship with the NSA, including its PRISM program, and they have also backed NSA-supported legislation that would make it easier to surveil Americans without a warrant. Similarly, Oracle is a longtime NSA contractor and also has ties to the CIA dating back to its earliest days as a company, not unlike Google. Notably, Oracle and Google remain locked in a major legal battle over copyright issues that is set to be heard by the Supreme Court in the coming weeks and is expected to have major ramifications for the tech industry.

To be continued?
Our work and existence, as media and people, is funded solely by our most generous supporters. But we’re not really covering our costs so far, and we’re in dire needs to upgrade our equipment, especially for video production.
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by Silviu “Silview” Costinescu

That is a fact. And it begs some questions.

THE FACTS:

The Universal Coronavirus Vaccine Patent.
DOWNLOAD PDF
2020 be like:
Source

THE QUESTIONS to anyone who believes in vaccines

  • Why does everyone act like it’s never happened?
  • If anyone claims it’s not good, how could’ve they known that in Februaty or in March, when the virus was “novel” and “the data was scarce”?
  • Can we expect to find more examples of either drug patents that don’t work or hidden medical and science advancements, whatever the case might be here?
Source

To be continued?
Our work and existence, as media and people, is funded solely by our most generous supporters. But we’re not really covering our costs so far, and we’re in dire needs to upgrade our equipment, especially for video production.
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