Update: Warp Speed and Hell Bound — White House


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Acquiesces to FDA’s…

Guidelines, COVID-19 Vaccine Emergency-Approval — Satan Soldiers are implementing a toxic vaccine

What’s That In Your Vaccine? The Rise Of The Xenobots!

There’s plenty of room at the bottom’, wrote Richard Feynman three days after I was born in 1959. In his talk to the American Physical Society, he considered the future development, not only of mass data storage, but also the development of nano-scale machines which could be used to manipulate single atoms. Synthetic chemistry if you like.

A month or so ago, I was intending to write an article on the use of nano technology which could enable workable electronics to be embedded into human cells. This was inspired by alternative media ideas of ‘smart dust’ and nano technology in the much-awaited SARS-CoV2 vaccine.

After a few days of research, I gave up on the idea. Not because nano machines don’t exist. They do. Although things work much better at the slightly larger scale of micro machines. At the nanometre level things can get bogged down with quantum effects and Van der Waals forces.

The whole point of such machines would be to communicate and manipulate data or deliver some targeted chemical which could be used for gene manipulation to modify the citizen’s behaviour or lifespan or simply just to remove tumours. All in all, an expensive and cumbersome task.

Psychological control is much easier than mere technology to control an unruly population which has the temerity to think for itself. Just look at the percentage of shoppers wearing a face mask at your local supermarket for proof of that.

There is no doubt that the Powers that Be consider a ‘sustainable’ population would be a significantly lower number than even we would even dare to guess at. They are, after all, nothing less than murderous psychopaths, but even that reduction in numbers could not be arrived at within any short space of time. Covid has been nothing more than a fart in the wind in terms of human death. So much for the zombie apocalypse.

If monitoring and controlling the citizenry is the aim, which it undoubtedly is for the World Economic Forum, the Feynman’s ‘Room at the Bottom’, should be reversed to ‘Room at the top’.

Nearly half of the world own ‘smart’ phones. For the other half that don’t, the Powers that Be don’t give a damn. They have no purchasing power.

The smartphone is your entry to the new digital world. If you use Android you are already hooked into the world run by Google. Similarly, for the iPhone. The data companies, Amazon, Netflix, Disney, know with a great deal of accuracy, where you are, what you are doing, what your pet’s name is, who your bets friends are, whether you will vote Labour or Conservative, where you will be tomorrow at 3p.m., what you eat for breakfast and if you are cheating on your wife/husband. That is, everything about you is known or can be known if they want to.

From your smartphone.

So where do Xenobots come in, how do they relate to smart dust and just what are they?

PNAS (Proceedings of the National Academy of Sciences of the United States of America) published this paper January 13, 2020: A scalable pipeline for designing reconfigurable organisms.

This is the abstract from the paper:

“Living systems are more robust, diverse, complex, and supportive of human life than any technology yet created. However, our ability to create novel lifeforms is currently limited to varying existing organisms or bioengineering organoids in vitro. Here we show a scalable pipeline for creating functional novel lifeforms: AI methods automatically design diverse candidate lifeforms in silico to perform some desired function, and transferable designs are then created using a cell-based construction toolkit to realize living systems with the predicted behaviours. Although some steps in this pipeline still require manual intervention, complete automation in future would pave the way to designing and deploying unique, bespoke living systems for a wide range of functions.

So, what does this mean?

The goal is to design a living organism with a specific function which will behave in the real world to “determine whether or how well behaviours (are) transferred from silico to vivo”.

What this means in simpler terms, is that a goal such as being able to move independently is defined and processed through an evolutionary algorithm (basically machine learning) from a few simple building blocks (the authors call them voxels, which is a 3d pixel) and arrives at designs which best fit that goal.

The computer designs are translated into living designs from the tissues of pluripotent stem cells from the blastula stage Xenopus laevis.

Pluripotent in this case means : Relating to or being a cell that is capable of differentiating into cells of any type of tissue except placental tissue.

Blastula in this case means: Embryonic development begins with a sperm fertilizing an egg cell to become a zygote, which undergoes many cleavages to develop into a ball of cells called a morula. Only when the blastocoel is formed does the early embryo become a blastula.

Xenopus laevis is: The African Clawed frog. Hence the name, Xenobots.

The creation of the new organism is shaped manually by

by subtraction using a combination of microsurgery forceps and a13-μm wire tip cautery electrode, producing a biological approxi-mation of the simulated design. Further, contractile tissue can belayered into the organism through the harvesting and embeddingofXenopuscardiac progenitor cells, an embryonically derived celltype which naturally develops into cardiomyocytes (heart muscle) and produces contractile waves at specific locations in the re-sultant shaped form 

So, from frog stem cells which are manipulated to conform into a computer designed form and using cardiac rhythms to perform movement, a biological nano machine is created.

There is no doubt that this is a remarkable achievement by the authors of the paper. It can be at worst said that it is proof of concept.

What I find remarkable is this excerpt from the paper:

The lifeforms presented here, despite lacking nervous systems, following novel developmental trajectories, and being composed of materials from different tissues, nevertheless possess these self-organizing properties. These properties synergize with and support the behaviour they were designed to exhibit. For instance, although signalling between cardiomyocytes was not enforced, emergent spontaneous co-ordination among the cardiac muscle cells produced coherent, phase-matched contractions which aided locomotion in the physically realized designs. Also, some of the designs, when combined, spontaneously and collectively aggregate detritus littered within their shared environment ….Finally, reconfigurable organisms not only self-maintain their externally imposed configuration, but they also self-repair in the face of damage, such as automatically closing lacerations …… Such spontaneous behaviour cannot be expected from machines built with artificial materials unless that behaviour was explicitly selected for during the design process

The Xenobots inspire much admiration in the science involved in their creation but also lead to questions, as do much of the ‘new’ biological sciences, fundamental questions on ethics.

The study itself was funded by DARPA but the uses for the new technology are, of course listed as the usual suspects: regenerative medicine, radioactive waste cleanup, scraping plaque from arteries etc. etc.

Smart dust is, in my opinion, not worth the bother as far as it can be used in biology. It would be expensive to manufacture and require significant electronic advances.

Xenobots? Well, what’s your opinion?


A scalable pipeline for designing reconfigurable organisms. Sam Kriegmana, Douglas Blackistonb, Michael Levinb, and Josh Bongard

Science Times Apr-3-2020 Staff Reporter

Wikipedia Xenobot

New York Times


About the author: Graeme McMillan graduated with Honours from Edinburgh University  (Politics, Philosophy and Economics) then gained further qualifications in Business Analysis, Project management, Statistics and Programming. He has had a long career in the UK mining industry in mine planning, geological modelling and computer systems management and programming. He then moved to the metals and minerals sector developing simulation modelling of materials handling (scrap, slag, semi-finished and finished products) as well as financial modelling of large mining and steel plant projects. Latterly, he ran his company’s Middle East and North African division. Graeme is now retired.

Update (1550ET): After the FDA stiff-armed the White House’s attempt to remove a provision from the public-health agency’s emergency use authorization guidelines, White House insiders are telling WSJ that they accept the FDA’s plan, bolstering claims made by FDA Director Dr. Stephen Hahn that the agency wouldn’t be swayed by Trump after appearing to kowtow to the administration.

Last night, both the NYT, Associated Press and Politico published “scoops” detailing an alleged effort from within the West Wing to improperly shape the FDA’s protocols and policies surrounding granting emergency-use authorization (EUA) to COVID-19 vaccines, with the goal of eliminating a provision that would effectively preclude a vaccine before election day.

Coronavirus tyranny end of liberty
FDA modernizes Nutrition Facts label for packaged foods ...

Politico’s report claimed that the White House was interfering at the behest of the big drug makers hoping for more lax restrictions.

Since they were published during President Trump’s return to the White House, the reports didn’t get much oxygen on cable news. But on Tuesday morning, the FDA surprised observes by releasing the new guidance.

Also, Bloomberg reported last night that the FDA had communicated its new standards directly to the drug makers, eliminating the need to release the new guidance, which was still under White House review.

A spokesman for the FDA told the press that the agency has already reviewed the requirements with individual manufacturers, and any interference with the guidance is really more of a PR issue.

“This does not change how the FDA would evaluate an emergency use authorization request for a Covid-19 vaccine,” said Michael Felberbaum, an agency spokesman. “The FDA has already communicated with individual manufacturers about its expectations, data the agency intends to consider, and what we expect to see in a request for an emergency use authorization to demonstrate safety and efficacy.”

But as the public backlash intensified, the FDA decided to release a document on its website Tuesday morning making clear that the requirement for two months’ of safety data would remain, as would a requirement for an independent panel of experts to weigh in on each candidate before a final decision can be made.

Here’s more from Bloomberg:

The document is the agency’s most detailed public statement yet on what it will take to get a vaccine cleared under a fast-track emergency use authorization, or EUA. The agency has been working on a separate “guidance” document that details the requirements, but it remains under review by the White House and it’s not clear when or if it will be released.

While the exact contents of that guidance document haven’t been released, the FDA has said that it’s already communicated the requirements to drugmakers. Publishing those requirements in the document released Tuesday essentially makes them public, even if the official document is lodged at the White House. It also makes clear that the FDA will add an extra step to the review.

In Tuesday’s document, the FDA said it will require an additional, follow-up meeting of its Vaccine and Related Biological Products Advisory Committee to look at specific applications by drugmakers. “This discussion will be specific to the particular vaccine that is the subject of the EUA request and will be separate from, and in addition to, any general discussion by the VRBPAC regarding the development, authorization and/or licensure of vaccines to prevent Covid-19,” the FDA said in the document.

Then again, whether the agency requires 8 weeks or 6 weeks of safety data may not make much of a difference. Vaccine approval is a tedious process that typically takes years. The speedy approval process virtually guarantees there will be no study of long term ramifications and side effects.

Yakira, LLC Trademarks (110) from Trademarkia - page 1

7 Billion Doses of COVID-19 Vaccine for World’s Population of 7 Billion Was This the Plan All Along?…

The COVID-19 pandemic has created an instant market for vaccine development. Around $1 billion of U.S. taxpayer funds have already been given to Big Pharma to develop the much coveted COVID-19 mRNA vaccine, a new class of vaccines that have never before been successfully developed. ($450 million to Johnson & Johnson in March, and $483 million to Moderna Therapeutics in April.)

At least another $2 billion is being spent by the Bill Gates-founded Coalition for Epidemic Preparedness Innovations (CEPI).

And this is all just for starters, as over 100 COVID-19 vaccines are currently in development by most of the world’s largest pharmaceutical companies. The CARES Act signed into law on Mar. 272020 allocates $27 billion for COVID-19 vaccine development, just in the U.S. alone.

And if that wasn’t enough, earlier this week (May, 2020) President Trump seemingly gave a blank check to spend as much as possible to fast track a COVID-19 vaccine through “Operation Warp Speed,” a coalition of scientists, government officials, military agencies, and private companies led by Alex Azar, the Health and Human Services Secretary, and Mark Esper, the Defense Secretary.

Their goal: to deliver 300 million doses of coronavirus vaccine from November to December 2020 and another 300 million by January 2021. (Source.)

So just by starting to research a COVID-19 vaccine, the already lucrative pharmaceutical industry just became the all-time most profitable industry on the planet.

As pharmaceutical companies compete with each other to get a COVID-19 vaccine to market, there was initial skepticism that an mRNA vaccine could be developed anytime soon. Projections were that it would take about 5 years, and even then only with a small chance of success. See:

Medical Analytics Firm: COVID19 Vaccine to Take 5.2 Years to Develop with 5% Chance of Success

Now, as we saw earlier this week with the announcement of the new “Operation Warp Speed” project, the projections are to produce enough vaccines to be able to inject all 350 million citizens of the United States by the end of 2020.

And on May 1st this week Moderna Therapeutics announced a partnership with Lonza manufacturing to start producing 1 billion COVID-19 vaccines a year.

Moderna Therapeutics is partnering with Dr. Anthony Fauci of the National Institutes of Health (NIH), who also has close ties to Bill Gates.

Bill Gates said in an interview this week that 7 billion vaccine doses are needed to end the COVID-19 pandemic, which is about the number of people currently living on the planet.

Will the entire world’s population just volunteer to get this vaccine, or are the drug companies counting on the fact that they will become mandatory?

The world’s largest manufacturer of vaccines, the Serum Institute of India, which produces 1.5 billion vaccine doses a year for an array of diseases, said it was not going to wait for approval of a COVID-19 vaccine, but would start manufacturing them immediately, starting with 40 million doses. They are currently working with the the Oxford Vaccine Group. (Source.)

It would seem that pharmaceutical companies manufacturing a COVID-19 vaccine are banking on the fact that the World Health Organization will recommend that they be mandatory.

Will the U.S. comply?

President Trump is the Key to Mandatory COVID-19 Vaccines in the U.S.?

There are good reasons why vaccine industry insiders balked at the idea of developing an mRNA vaccine so quickly initially. They have tried to develop them in the past, with dismal results. They were unsuccessful in trying to develop this kind of vaccine for other coronaviruses, like SARS and MERS.

Dr. Fauci and the NIH, working together with Bill Gates, also previously had dismal results in developing this kind of vaccine for HIV/AIDS.

But all of that has now changed with the world-wide “plandemic” of COVID-19.

President Trump can now eliminate safety tests normally required for FDA approval of drugs and vaccines, by invoking the “Emergency Use Authorization” authority which “allows FDA to help strengthen the nation’s public health protections against CBRN threats by facilitating the availability and use of MCMs needed during public health emergencies.”

According to the FDA website:

Under section 564 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), the FDA Commissioner may allow unapproved medical products or unapproved uses of approved medical products to be used in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions caused by CBRN threat agents when there are no adequate, approved, and available alternatives.

Section 564 of the FD&C Act was amended by the Project Bioshield Act of 2004 and was further amended by the Pandemic and All-Hazards Preparedness Reauthorization Act of 2013 (PAHPRA), the 21st Century Cures Act of 2016, and Public Law 115-92 of 2017.

President Trump invoked this authority this week (May, 2020) in directing the FDA to approve the anti-viral drug remdesivir, which was previously abandoned as a treatment for Ebola.

“I’m pleased to announce that Gilead now has a EUA (emergency use authorization) from the FDA for remdesivir — and you know what that is, because that’s been the hot thing also in the papers and in the media for the last little while,” the president said.

FDA Commissioner Stephen Hahn confirmed the authorization “was issued today.” (Source.)

This is like a dream come true for pharmaceutical companies. A pandemic allows them to secure government funds to research new drugs.

It allows them to bypass normal FDA safety testing with legal immunity should things go wrong and people are injured or die from the side effects.

Then the government, who paid for the research and development, ends up spending more of your taxpayer funds to purchase these vaccines through the CDC, and then requires the American population to receive them, while selling the excess vaccines produced that the American public does not use to the World Health Organization to be mandated upon citizens of other countries.

With the announcement earlier this week that Moderna Therapeutics has developed a partnership with Lonza manufacturing to start producing 1 billion COVID-19 vaccines a year, it would seem that they are the leading candidate at this point to benefit the most, especially since they are working in partnership with Dr. Anthony Fauci, a member of President Trump’s Coronavirus task force team.

The Moderna – Lonza partnership was huge news this week, as Fauci said back in February that even if they had a vaccine that would work, it would be difficult to produce so many so quickly:

Production would require an amount of time that’s as “problematic” as developing the shot itself, Fauci said. (Source.)

Fauci also allegedly stated that once Moderna reached phase 2 testing of the vaccine, that it would be tested in China, suggesting that he is still working closely with the World Health Organization, and looking at supplying his COVID-19 vaccine to the entire world. (Source.)

Do you want to be required to receive an experimental COVID-19 vaccine that has been fast-tracked and where the drug companies have no risk or liability should anything go wrong?

If not, President Trump is the probably the only one who can stop this, and it is time that the American public lets him know that we will not comply.

These Governors and Politicians Are Caught up in Their Own Destruction, the Plandemic of All Scamdemic Has Turned on Its Creators and Will Wreak Havoc…

Satan Soldier Mr. Gates : the vaccination certificates “will probably have to be internationally recognized in order to allow travel, international travel.”

They went on to make it clear that people who take the vaccine will see their lives return to normality while those who don’t will still be “subject to social distancing rules.”

The prospect of denying basic rights of mobility and travel to people who refuse to take a vaccine for personal, religious or medical reasons is shaping up to be a human rights minefield.

The World Is In Big Trouble, for Those That Believe We Will Go Back to Some Sense of Normal Life Here on Earth, You Will Be Sadly Disappointed, Seven Years of Hell on Earth Which Began January 1, 2020

“Our courts oppose the righteous, and justice is nowhere to be found. Truth stumbles in the streets, and honesty has been outlawed” (Isa. 59:14, NLT)…We Turned Our Backs On GOD, Now We Have Been Left To Our Own Devices, Enjoy…

While Mainstream Media Continues to Push a False Narrative, Big Tech Has Keep the Truth From Coming out by Shadow Banning Conservatives, Christians, and Like-Minded People, Those Death Attributed to the Coronavirus Is a Result of Those Mentioned, They Truly Are Evil…

Source: HNewsWire ZeroHedge HNewsWire HNewsWire HNewsWire HNewsWire HNewsWire

StevieRay Hansen
Editor, HNewsWire.com
Watchmen does not confuse truth with consensus The Watchmen does not confuse God’s word with the word of those in power…

In police-state fashion, Big Tech took the list of accused (including this site), declared all those named guilty and promptly shadow-banned, de-platformed or de-monetized us all without coming clean about how they engineered the crushing of dissent, Now more than ever big Tech has exposed there hand engaging in devious underhanded tactics to make the sinister look saintly, one of Satan’s greatest weapons happens to be deceit…

The accumulating death toll from Covid-19 can be seen minute-by-minute on cable news channels. But there’s another death toll few seem to care much about: the number of poverty-related deaths being set in motion by deliberately plunging millions of Americans into poverty and despair.

American health care, as we call it today, and for all its high-tech miracles, has evolved into one of the most atrocious rackets the world has ever seen. By racket, I mean an enterprise organized explicitly to make money dishonestly.

All the official reassurances won’t be worth a bucket of warm spit. The Globals are behind the CoronaVirus, It Is a Man-Made Bioweapon.

We have had nearly eight months of life and liberty stolen from us by politicians and their hysteria-promoting accomplices in media. How much more will we accept?

A virus is not a disease. Only a very small percentage of those exposed to the virus itself – SARS-CoV-2 – show any kind of acute respiratory symptoms, or what we can call “coronavirus disease.” 

The only meaningful statistics show the incidence of serious illness, hospitalizations, and deaths. The single most important statistic among these is the infection fatality rate (IFR). Data collected through July shows that the IFR for those under age forty-five is actually lower than that of the common flu. The covid-19 IFR rises for those over fifty, but it is hardly a death sentence. And the data does not segregate those with preexisting health issues caused by obesity, diabetes, and heart disease. If we could see data only for reasonably healthy people under fifty, the numbers would be even more reassuring. 

Mild or asymptomatic covid cases are effectively meaningless. The world is full of bacteria and viruses, and sometimes they make us a bit sick for a few days. There are millions of them in the world all around us, on our skin, in our nose and respiratory tract, in our organs. We are meant to live with them, which is why we all have immune systems designed to help us coexist and adapt to ever-changing organisms. We develop antibodies naturally, or we attempt to stimulate them through vaccines, but ultimately our own immune systems have to deal with covid-19. The virus will always be out there waiting, on the other side of any lockdown or mask—so we might as well get on with it. 

From day one the focus should have been on boosting immunity through exercise, fresh air, sunlight, proper dietary supplementation, and the promotion of general well-being. Instead our politicians, bureaucrats, and media insisted on business lockdowns, school closures, distancing, isolation, masks, and the mirage of a fast, effective vaccine. As with almost everything in life, state intervention made the situation worse. We can only hope many governors are removed from office, either by impeachment or at the next election. Several, including Andrew Cuomo in New York and Gretchen Whitmer in Michigan, should face criminal charges for their lawless edicts. There is no due process exception for “public health.”

Lockdowns were never justified, either in terms of the covid-19 risk or the staggering economic tradeoffs, which will be felt for decades. They certainly are not justified now, given seven months of additional data showing that the transmission and lethality of covid-19 are not particularly worse than previous SARS, swine flu, or Ebola pandemics. We still don’t know how many of the reported two hundred thousand US covid-19 deaths were actually caused by the SARS-CoV-2 respiratory disease, or simply reflect people who died of other causes after exposure to covid-19. We do know that the harms caused by the lockdowns far outweigh the harms posed by the covid-19 virus.


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  2. Patrick Galasso on October 7, 2020 at 1:40 pm

    The planning for the next stages of study for Moderna was supported by funding from the US Biomedical Advanced Research and Development Authority (BARDA), which came from a deal worth up to $483 million announced a few weeks ago. The BARDA funding will also go towards supporting the late-stage clinical development programmes, as well as the eventual scale-up and expansion of mRNA-1273 manufacturing.

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