UK and US Jointly Develop Biological Weapons
By Vladimir Platov – New Eastern Outlook – 14.03.2022
Documentary evidence of Washington’s aggressive plans for developing and manufacturing biological weapons in secret US biological laboratories in Ukraine, banned by international conventions, has been uncovered during the Russian special operation to denazify and demilitarize Ukraine, and it is frankly horrifying! Although suspicions of such US activities have already been repeatedly published by many media outlets and their verification and official confirmation of such criminal anti-human plans by Washington was one of the goals of Moscow’s special operation to demilitarize Ukraine.
In this regard, the former weak position in bringing clarity to the exposure and suppression of such forthcoming US crimes is highly surprising. First of all, the international community and international institutions should have long ago initiated an independent inspection of some 400 such secret Pentagon biological laboratories scattered around the world, whose location in specific countries is clearly linked to the theatres of future US military action against “adversaries.”
The unconditional involvement of Britain, which has long collaborated with the US in the development of chemical and biological weapons, has also surprisingly been ignored in relation to such criminal plans.
Thus, the US Federal Contractor Registry shows that the Pentagon has spent more than $70 billion in recent years alone on experiments with deadly viruses and nerve agents at the Porton Down military biological laboratory, which is located near Salisbury in Great Britain. The US Defense Threat Reduction Agency (DTRA), led by the US Department of Defense, has funded a number of defense projects at this so-called “Defense Science and Technology Laboratory” (DSTL) at Porton Down. These include experimental infection of primates with anthrax, Ebola, Marburg, Venezuelan equine encephalitis, western and eastern equine encephalitis viruses, and poisoning of animals with mustard gas and phosgene. It is well known that experiments with LSD have been “incapacitating” British troops during exercises. The testing of chemicals on humans, however, was not out of the ordinary for Porton Down. According to El Pais, in 1963 Porton Down staff decided to test the vulnerability of public infrastructure to chemical and biological attacks by spreading a bacterium on the London Underground, which was initially thought to be harmless but turned out to be quite capable of causing septicemia.
The DTRA has full access to all scientific and technical developments at the Porton Down “laboratory.” Such experiments involving animals are considered secret in Great Britain and it is a criminal offence under Chapter 24 of the Animals (Scientific Procedures) Act to reveal information about such experiments.
According to information received by the media, military experiments with chemical and biological weapons have increased at Porton Down in recent years. Thus, between 2005 and 2016, 122,000 animals were infected with deadly viruses or poisoned with chemicals. The “laboratory” uses mice, guinea pigs, rats, piglets, ferrets, sheep and monkeys in its research.
It is also known that British military “scientists” received funding from the DTRA to develop a chemical testing system from 2012 to 2017, with experiments on the effects of VX and VM poisoning agents being conducted at Porton Down in 2015.
In 2013, scientists from Porton Down sprayed gas on the London Underground, which the British government tried to keep quiet about and not tell its citizens. At the time, thousands of persons were gassed without their knowledge, and no one asked for their consent to take part in such barbaric “research” against their own people. Nevertheless, data about this is recorded in a British Home Office document, telling also about other programs conducted jointly by the United States and Britain.
Information about the UK’s Defense Science and Technology Laboratory (DSTL) testing of the chemical poison VX on guinea pigs was posted on the US National Center for Biotechnology Information website on August 9, 2018. And on September 1, 2018, a report emerged on behalf of 10 more researchers at the DSTL about testing Bioscavenger, which is an effective delayed therapeutic intervention for VX chemical weapons poisoning. The DSTL itself officially admitted in mid-2016 that they were producing the poisonous substance and testing it on animals. The DTRA is a major foreign client of the UK’s DSTL. Between 2012 and 2017, British military scientists received $39.7 million for the Pentagon’s chemical system testing program, and judging by the US Federal Procurement System, the DSTL and DTRA collaboration continues.
The Porton Down secret laboratory has repeatedly been at the center of scandals involving human experimentation. Up to 20,000 people participated in litigation with the DSTL from 1949 to 1989. And in 2008, the UK Ministry of Defense paid 360 veterans £3 million without admitting responsibility.
According to The Guardian, in the late 2000s, the US and Britain experimented with biological weapons in Afghanistan, using a specially bred fungus called fusarium oxysporum and pleospora papaveracae to kill poppy crops. In 2000, the international NGO Sunshine Project published a report on the danger of this fungus infecting and killing not only coca, poppy and cannabis, but also other plants in environmentally sensitive areas of Asia and the New World. An indication of the dangers of such fungi is the fact that their use is banned in the US. According to the Sunshine Project report, genetically modified strains of the fungus have been bred in the US, which means that the deliverables can be classified as biological weapon.
Given this information alone, the extent of Britain’s involvement in the possible development with the US of biological weapons already needs to be investigated in detail.
The story of patient 11281009 in the Pfizer trial
Some disturbing findings hidden in the reluctantly released data
Health Advisory & Recovery Team | March 11, 2022
After a Texan court ordered the FDA to release the documents used to approve the covid vaccine the first 150 documents have now been published. These include the medical notes for a selection of patients at five different trial sites. Sonia Elijah has carried out part 1 of a forensic analysis of the patient notes and noted some disturbing findings, for a number of patients.
The story of patient 11281009 is just one example. Patient 11281009 was a white male who would have turned 66 years of age in 2020. By piecing together the entries in the system and the audit log querying errors in those entries it is possible to recreate a timeline of events (see below).
In summary, after two doses of either vaccine or placebo by 9th August, he presented to the emergency room with cough and shortness of breath. This presentation was recorded as suspected covid. He had a myocardial infarction and developed a pneumonia during his stay. No details of covid testing were recorded but the family reported a single negative test taken during his hospital stay. He was discharged home where he died sometime between the end of October and beginning of February. No explanation was given for why hospital treatment was abandoned; remember you had to be “healthy” to enroll in the trial. The death certificate was said to have recorded the cause of death as “pneumonia”.
His last contact with the trial site was 16th September 2020. The trial protocol included participants having an app on their device to enter any covid-like symptoms but there is no entry of this in trial medical record. His family phoned the site on or around 8th December and relayed the details of his last weeks. These were entered in a “potential covid 19 form” by the site. However, the date of this entry was after death. For this reason all the details of the clinician’s concerns around him having had covid were expunged retrospectively from his records in the trial.
To reiterate, this patient had a cough, shortness of breath and presented to hospital with suspected covid, developed pneumonia, died of it and all records of this presentation except hospitalisation then death from “due to infection” were removed from the trial.
The inability to ensure accurate records are kept and to test people with suspected covid raises real concerns about the accuracy of the trial data. Even after 6 months, up to March 2021, only 2.2% of people enrolled in the trial were said to have had covid. However, there were 3410 cases of “suspected covid” (7.3% of the vaccine arm and 8.4% of the placebo arm). For comparison, Public Health England estimated that 15% of the population had had covid over the year up to end of March 2021, based on antibody testing which may underestimate the total. Why enroll 44,000 people into a trial and then fail to diagnose the disease of interest? How much bias was introduced by failure to test?
We recommend you read the timeline of events below. It tells a disquieting story and as yet, we do not know how many other details of the trial might ultimately be seen as ‘troubling’ at best. With billions of dollars at stake, involving the company who once paid a fine of $2.3 billion, $1.3 billion of which was a criminal fine, let us not be naive enough to think that ‘health and well-being of the nations’ was Pfizer’s primary goal in their rushed product roll-out.
TIMELINE
27th July 2020: Pfizer selects molecule for testing.
31st July 2020: He was screened, consented, enrolled, randomized, swabbed and injected with a first dose. This may have been placebo or vaccine. Something odd happened with his consent which was described as “unknown or N/A” (see pg 352) but marked a “obtained” eventually.
19th August 2020: He had a further nasal swab and received a second dose.
Nothing is then entered in the record until 8th December. When this entry appears:
27th October 2020: He had a Myocardial Infarction and was hospitalized. This was recorded as a serious adverse event. In response to the question “Is this event related to treatment?” was the response “Not related. Due to – other – failed cardiac stent.”
28th October 2020: The following day he remained in hospital with life threatening pneumonia. In response to “Is this event related to treatment?” was the response “Not related. Due to – other – infection.”
At some point between the end of October and 9th December 2020 the patient died at home (pg 333). The entry saying he died at home is still in the audit trail but the form where this information was uploaded is not present in the patient record. The cause of death was entered on 13th January 2021 as “pneumonia”. There is no record of the length of hospital stay or why he was discharged before death.
18th Nov 2020: Pfizer published a press release claiming over 94% efficacy of the vaccine.
2nd December 2020: MHRA authorises vaccine for emergency supply.
8th December 2020: Four issues were raised.
- That the adverse event had been recorded as “fatal” but no death form was recorded (pg 349).
- No serious adverse event number had been entered for either the myocardial infarction or the pneumonia (pg 345)
- It was suggested that the myocardial infarction entry should be changed from a serious adverse event to a “worsening adverse event” on the basis that he had had a previous myocardial infarction in 2017 (pg 337).
- It was noted that the serious adverse event had been marked as “recovered or resolved” in the safety database despite the death of the patient (pg 341).
9th December 2020: The file is marked as “discontinued”.
13th December 2020: The gentleman’s relatives telephone the centre to tell them about the lead up to his death (pg 301 to 303). It seems someone is unsure how to enter this information and is advised:
“Potential COVID-19 related PNEUMONIA should have please triggered a COVID Illness Visit irrespective of perceived etiology or clinical significance. Please complete the COVID-19 CRF forms. Please complete the potential COVID-19 Illness Visit CRF forms with all information available. Should be captured only on the SOD CRF form and a NASAL SWAB will not be collected. Please the data should still be captured on the appropriate CRF pages (as for any late data, we will still capture it and not ignore it) but a swab will not be required” (pg 345-6)
14th December 2020: The person wanting to record this information opens up a “potential covid 19 visit form”. The audit trail then spits out a complaint that no swab was taken, no sign or symptom form was completed and this form was dated after the file had been discontinued. Someone patiently filled out the explanation that the patient was deceased and these were not possible for each of these entries.
The audit trail shows that the data entered on this date included that the patient had a cough, shortness of breath but no loss of smell or taste, diarrhoea or vomiting, (pg 308) and had been seen in the emergency room (pg 324) for a “potential covid 19 illness” (pg 329).
31st Dec 2020: Pfizer released their NEJM paper of the trial results. No covid deaths were reported to have taken place.
19th January 2021: Query raised that the covid illness form was dated 14th December 2020 after the subjects death. The site responded to this saying,
“The symptoms were reported to site after subject’s death via subject’s family, per medical monitor, this data is to be entered.”
22nd January 2021: He was due to be unblinded in the trial and offered a vaccination if he had been in the placebo arm.
26th January 2021: The site were told:
“There cannot be a date later than the date of death. Please remove data from the COVID Illness visit and add COUGH and SHORTNESS OF BREATH as AEs… COVID_A visit should then be marked as ERRONEOUS.”
28th and 29th January 2021: Attendances for nasal swab and antibody testing were marked up individually as “not applicable” and then an entry stated that he had “withdrawn consent” presumably to prevent these repeated requests for more data.
15th February 2021: The site were told:
“For correct attribution of Pneumonia; please update AE term to COVID Pneumonia or Pneumonia secondary to COVID-19 else clarify as per guidance from Clinical Monitor” (pg 344)
And
“We need to remove the COVID Illness visit which was originally requested. Please mark Erroneous and remove the data from within the visit using FORM Level comments of NOT APPLICABLE.” (pg 299)
27th February 2021: The site responded:
“SITE HAS NOT BEEN MADE AWARE THIS EVENT WAS COVID PNEUMONIA. PER PI PNEUMONIA WAS RELATED TO INFECTION, HOWEVER SITE HAS NO RECORDS THAT STATE COVID, THEREFORE TERM CANNOT BE UPDATED TO SUCH.” (pg 344)
2nd March 2021: “Site has not received MR (medical record) and cannot confirm a COVID test was done, however per family of subject, there was a negative COVID done, sometime during hospital stay, not sure which day or which test.” (pg 316)
How to measure vaccine harms
Health Advisory & Recovery Team | March 11, 2022
Drug harm reporting systems, like the MHRA’s yellow card system, are designed to alert the regulator to a potential issue. They are not designed to measure the size of the problem. If an issue is highlighted then the regulator has a responsibility to carry out an audit and see whether the incidence of the condition of concern has been higher than historical levels in the population who were vaccinated.
The Government appears to be treating the yellow card reports as if they are a record of every occurrence of a condition in the country, comparing the number of reports with background levels in the whole population. It is well known that reporting systems only capture a fraction of cases and it is very odd that the Government is treating this data as comprehensive.
As an example, let’s take Guillain-Barre Syndrome (GBS) which is a rare condition where the immune system attacks the nervous system. It is usually caused by a viral infection but has been attributed to vaccination adverse reactions in the past. There are 1,300 cases every year and 608 cases have been reported on the yellow card system.
A study by Hanson et al in the USA of 10 million patients showed that in the first 21 days after the Oxford-AstraZeneca vaccine the rates of GBS were 15 times higher than expected levels. Extrapolating from this figure we would expect 500 AZ vaccine related cases in the UK. There have been a total of 488 reported in the yellow card system but it is not clear whether these were within 3 weeks of vaccination.
In a three week period we would expect 29 background cases to have occurred co-incidentally. Based on the Hanson data of 500 cases after 24.9 million doses, the cause of someone having GBS within 3 weeks of the Oxford-AstraZeneca vaccine would be the vaccine 95% of the time and coincidental 5% of the time. The morally right thing to do for these people, is to accept that they have been vaccine injured and be wrong 5% of the time rather than claim these were coincidental and be wrong 95% of the time.
The Government appears to want to claim coincidence. A few of these patients have filed claims with the Vaccine Damage Payment Scheme. None of the claimants have been helped, even patients whose deaths have been investigated at inquest and where a coroner has determined the vaccine as the cause of death. When rolling out a £12bn vaccine programme it is naive not to set aside a budget for vaccine injury. The current claims system requires proof of “60% disability”, a ‘proof of cause’ and does not compensate for lost earnings or costs of care. Maria Caulfield, the minister for patient safety and primary care, said that they were employing people to look through the claimant’s medical records for a “causal link” as if vaccines write confession notes. Surely, this is the real waste of public funds and seems to point to a reluctance to compensate deserving victims.
Another predicted spike in heart attacks (but it’s still nothing to do with the vaccines)
By Kit Knightly | OffGuardian | March 11, 2022
This past week saw two high-profile Australians – cricketer Shane Warne and Labour senator Kimberley Kitching – both die of sudden heart attacks aged 52.
As such, heart disease is back in the headlines. Again.
We predicted in our new-years post that explaining heart attacks would be a big part of 2022’s news cycle, and only three months in it has been a torrent.
It actually started in December of 2021, with medical doctors theorising that the stress and anxiety of dealing with Covid was going to cause a huge spike in heart problems due to “post-pandemic stress disorder”.
Before the end of January, the media were reporting that aortic stenosis was actually massively under-diagnosed and we could see up to 300,000 new cases of heart disease or damage in the near future.
At the beginning of February, a new reason was added to the list. As energy prices began to spike – do remember, that happened before the war – we were told the increased cold and stress could also cause heart disease.
Then, in mid-February scientific papers appeared claiming that “even a mild case of COVID” causes your “heart attack risk to soar”.
In short, and for many reasons, you’re much more likely to have a heart attack this year than you were last year.
Well, now the Sydney Morning Herald has joined in, with this article headlined “‘This is our biggest killer’: Shock deaths put spotlight on heart disease”, which warns:
The shock deaths of cricketer Shane Warne and Senator Kimberley Kitching should serve as a wake-up call to Australians about the prevalence of heart disease, doctors say, as a study shows COVID-19 may increase the risk for what was already one of the nation’s biggest killers.
Yes, having had covid – even if you just tested positive and had no symptoms – makes it more likely you’ll have a heart attack.
On top of that, warn the doctors quoted in the article, thousands of people will have missed their heart screenings due to lockdown, or have been sedantry and gained weight, not to mention the anxiety and stress.
All in all, Australians can expect a “rise in preventable heart disease deaths over the next five years”, according to health modellers.
But don’t worry, none of that is anything to do with the untested vaccines they’ve injected into literally millions of people.
Yes, all the major Covid vaccines are known to have “rare” side effects that impact the heart, such as blood clots and myocarditis, but clearly, that’s just a coincidence.
After all, the Sydney Morning Herald article doesn’t even use the word “vaccine”, not one single time. And they wouldn’t ignore anything that important, would they?
$1.5 trillion federal spending bill allocates $2.6 billion to programs that fight “disinformation” and “hate”
By Tom Parker | Reclaim The Net | March 11, 2022
The huge $1.5 trillion US federal spending bill, that’s expected to be signed into law by President Joe Biden today, allocates over $2.6 billion to “Democracy Programs” and requires these programs to combat “the misuse of social media to spread disinformation or incite hate.”
This requirement is buried deep into the 2,741 page bill on page 1,408 and is part of the “Title VII General Provisions” of the “Department of State, Foreign Operations, and Related Programs Appropriations Act, 2022.”
The bill states: “Democracy programs supported with funds appropriated by this Act… should, as appropriate… include… efforts to combat weaponized technology, including the misuse of social media to spread disinformation or incite hate.”
While this is the main requirement in the bill related to disinformation, there’s also another reference to disinformation on page 1,848 that states:
“Funds appropriated by this title under the heading “Economic Support Fund” may be transferred to, and merged with, funds available under the heading “Diplomatic Programs” for activities related to public engagement, messaging, and countering disinformation.”
The “Economic Support Fund” heading makes $6.47 million available until September 30, 2024 while the “Diplomatic Programs” heading makes $125 million available until September 30, 2024 with the provisions that up to $15 million “may be transferred to, and merged with, funds available under the heading “‘Capital Investment Fund”’ for cybersecurity and related information technology investments” and that the funds “shall be made available, as appropriate, to enhance the capacity of the Department of State to identify the assets of Russian and other oligarchs related to the situation in Ukraine, and to coordinate with the Department of the Treasury in seizing or freezing such assets.”
We obtained a copy of the bill for you here.
The way the final text of this massive spending bill was released in the middle of the night, hours before a final vote, has been criticized by numerous US politicians.
The final text of the bill was published just before 3 am Eastern Standard Time (EST) on Wednesday morning and the final vote for the bill in the US House of Representatives was set for 1:30 pm EST on Wednesday, giving representatives less than 11 hours to read the final text before voting.
A day later, the final vote for the bill in the US Senate was held, giving Senators around 24 hours to read the nearly 3,000 pages in the bill.
“Literally in the DARK OF NIGHT, the Democrat controlled Rules Committee met at 1:30 am – 2:30 am and passed the HORRENDOUS $1.5 TRILLION Omnibus bill,” Rep. Marjorie Taylor Greene tweeted. “They did NOT tell anyone or announce this debate on the bill until after midnight! We woke up to 2,741 pages and we vote today!”
Senator Rand Paul added: “Do you think there is a single person in the U.S. who believes that Congress is filled with speed readers capable of digesting thousands of pages in a matter of hours? The 2741-page omnibus with a $1.5 trillion price tag that was released in the middle of the night is a perfect example of why Congress needs time to read the bills.”
This isn’t the first time a huge spending bill has been used to push new online rules. In December 2020, a controversial copyright reform that proposed up to 10 years in prison for “unauthorized streaming” was buried 2,540 pages deep in the 5,593 page “Consolidated Appropriations Act, 2021.” Despite its huge length, this bill passed both houses of Congress and was signed into law by then-President Donald Trump within six days.
The addition of requirements to fight online disinformation in this federal spending bill is the latest of many examples of the federal government targeting online speech. The Biden White House has admitted that it flags content for Facebook to censor and proposed that If you’re banned for “misinformation” on one platform, you should be banned from ALL platforms. Members of Congress have also threatened to hold Big Tech companies “accountable” if they don’t censor misinformation.
Moscow rejects Washington’s chemical-weapons claim
RT | March 12, 2022
Russia’s ambassador to Washington accused the Americans on Saturday of trying to “demonize” Moscow, rejecting a US State Department allegation that his country may deploy chemical weapons in Ukraine.
“The US official, as always, did not bother to provide any evidence. This is another attempt to demonize our country,” Anatoly Antonov said, adding that such claims were “not worth a penny.”
Citing a paper from Russia’s Ministry of Foreign Affairs, the official then suggested that Ukrainian “radical groups” – allegedly “[trained] under the control of the representatives of American special services” – could have themselves “prepared several potential scenarios of the use of toxic chemicals in order to carry out various types of provocations.”
“Our country, unlike the United States, eliminated all available stocks of chemical warfare agents in 2017. This fact has been documented by the OPCW. It is pointless to argue with this fact,” Antonov concluded, in reference to the fact that US chemical warfare stockpiles have yet to be completely decommissioned.
The Russian government has claimed that Ukrainian groups backed by the US could be preparing a false-flag chemical attack in order to “accuse Russia of the use of chemical weapons against the civil population and violating its obligations.” The US and Ukraine have denied such claims.
State Department spokesperson Ned Price suggested on Wednesday that Russia could use chemical weapons in Ukraine.
“Russia has a track record of accusing the West of the very crimes that Russia itself is perpetrating,” he said, calling Moscow’s warnings “an obvious ploy.”
White House Press Secretary Jen Psaki claimed this week that Russia could “use chemical or biological weapons in Ukraine” or “create a false-flag operation” with such weapons. Psaki added that the world should “be on the lookout.”
Psaki dismissed Moscow’s suggestions that the US and Ukraine could conduct a similar false-flag attack, calling them “false claims” and “conspiracy theories.”
The press secretary argued that Moscow’s claims were an “obvious ploy” to justify further military action in Ukraine.
Russia’s Foreign Ministry claimed on March 6 that Russian forces had discovered evidence of Ukraine erasing traces of an alleged US-backed military biological program in the country. Washington has claimed it is working to prevent Russian forces from capturing biological research material.
Reality Check: “100 day vaccines” are NOT possible
By Kit Knightly | OffGuardian | March 11, 2022
Neatly nestled behind the Ukraine headlines plastered all over the front pages, this past week has seen the World Health Organization meeting to discuss the global legislation to empowering the WHO to combat “future pandemics”.
The first consultation was held on March 1st. The EU passed a motion authorizing the bloc to negotiate such a treaty on March 3rd.
Nobody knows exactly what the hypothetical international regulations – dubbed the “Pandemic Treaty” – would entail, but there are hints.
It’s almost certainly going to involve some kind of international vaccine passport, possibly based on the SMART Health Cards currently rolling out all across the US.
It’s also interesting to note that this treaty is being developed in parallel to the UK “reforming” their Human Rights Act 1998 into a new “UK bill of rights” which seeks to prevent the “abuse” of “rights culture” and place a new emphasis on “social responsibility”.
However, the specifics will remain a mystery until the final proposal is published later this year.
One thing we do know though, is that a big part of the proposed “strengthening” of our pandemic response will be increased funding and resources for developing vaccines even faster than the Covid vaccine.
This aim was announced at the recent Global Pandemic Preparedness Summit in London, where the Coalition for Epidemic Preparedness Innovations (CEPI) announced their “100 Days Mission”.
CEPI, for those who don’t know, is a foundation jointly funded by (among others) the Bill and Melinda Gates Foundation and the World Economic Forum, whose stated aim is “to develop vaccines to stop future epidemics”.
The 100 Days Mission, which already has its own website and a trending hashtag (#100DaysMission), is pretty much exactly what it sounds like.
In future CEPI wants to produce new vaccines for unknown emerging diseases – what they call Disease X – within 100 days of the pathogen being isolated.
They’ve already secured 1.5 BILLION pounds sterling to further this effort.
Let that percolate.
Over a billion pounds to produce vaccines for a disease that – as yet – does not even exist, and may never exist.
This looks like a further step in the process, begun by the ‘pandemic’ narrative, of redefining everything we previously understood about how infective agents and vaccines interact.
Covid, let’s remember, was a disease-narrative totally removed from all social, scientific and historical context to create a fluid, agenda-driven alternate reality. And it looks as if this is intended to be the ‘new normal’.
Here’s a little refresher course on just how fast the Covid vaccines sped through the usual scientific process:
- The virus was allegedly discovered in December.
- It was fully genetically sequenced by January 10th 2020.
- The paper that all the PCR tests were based on was peer-reviewed in less than 24 hours.
- After decades of failure, the human race produced a dozen effective coronavirus vaccines in less than three months.
- These vaccines were then “safety tested” in less than six months.
All told, from ‘discovering’ the virus to getting the vaccine(s) approved for use on people, it took 300 days.
This process normally takes at least 3-10 years.
It usually takes at least 5-10 years to bring a fully-tested vaccine to market. A paper by Pronker et al, “Risk in vaccine research and development quantified” (PubMed 2013), estimates the average development time for a new vaccine to be over 10 years.
Simply put, it has never been possible to make a vaccine for a new disease in 1000 days, let alone 100.
The speed with which the covid vacines were produced is totally unprecedented in the history of vaccines.
The idea you could further reduce this unprecedented time frame, and produce a safe and effective vaccine in only 100 days is frankly absurd. It’s surreal. Fictional.
For one thing, the vast majority of candidate vaccines don’t work.
The Pronker paper, found that of all potential vaccines products being researched, only about 6% ever actually hit the market.
So, back in the real world, a vaccine manufacturer will go through that 5-10 year process knowing there is a ~94% chance there will be nothing to show for it in the end.
After decades of trying they haven’t managed to produce a vaccine against AIDs, or the flu, or malaria or many other common diseases. These are conditions they know and (allegedly) understand, but they cannot make vaccines for them.
So, in that old world of veridical reality, even if you managed to make a vaccine in 100 days, the odds are it either won’t produce immunity, or it will but will also produce harmful side effects, or maybe it will do literally nothing.
Now, granted, science and technology are not static. We are always moving forward and making progress… but that’s irrelevant to this issue, because even if vaccine manufacturing technology really did take a huge leap forward just in time to battle covid, you still can’t produce a safe vaccine in 100 days, or even 300 days – because the process NEEDS time.
It takes time to test rigorously, it takes time – a lot of it – to a assess long term side effects. The clue is right there in the name.
No amount of new tech is going to permit you to know the ten-year effects of a vaccine in under three months.
With the public eye fixed on Ukraine, and Covid now firmly in the collective unconsciousness’s rearview mirror the powers that be are trying to normalise what was, inherently, an abnormal, unreal (if not impossible) process. To make it easier “next time”.
We’ve already seen Bill Gates lament that the vaccine was too slow, and he was partially right. The Covid story didn’t keep people hypnotized enough to secure everything they needed, in part because their “vaccine” rollout took almost a year.
But for the future “Disease X” waiting in the wings, it will officially only take three months, and the fear will still be fresh. The fact the process will be completely incompatible with reality or sense will not matter in the slightest.
To be clear: You cannot develop a “safe and effective” vaccine for a brand new disease in three months.
You can’t do it in one year.
And if in the future they claim to have done so, they will be lying.
US Enriches itself at the Expense of the EU Paralized by the Price Shock
By Vladimir Danilov – New Eastern Outlook – 09.03.2022
Europe has been shaken by galloping gas prices in recent months, leading to financial and socio-political instability in the Old World.
There are several reasons for this, one of them being the politics of domestic European speculators, who wanted to get rich quick when, as a result of their blatant Russophobic policies, European officials managed to keep Gazprom and its cheap gas out of the EU internal market. As a result, these speculators sell at a markup of 300, 400 or 500 per cent the cheap gas that Gazprom pumped into their storages back in the summer. In doing so, they squeeze their super-profits out of the European consumer. And until they sell these reserves, they will not let Russian gas into Europe.
In addition to European speculators on Russian gas, the United States has become enormously rich in recent months, profiting from the extraordinarily high prices. Meanwhile, in order to distract public opinion from the true situation on the issue, Joe Biden’s administration officials are trying to falsely accuse Moscow of increasing gas prices, while doing nothing to lower those prices themselves, as their fall is absolutely unprofitable for Washington.
And this is confirmed by data from the Russian Federal Customs Service and the US Bureau of Economic Analysis, which clearly show reports on gas exports to Europe by the US and prove that it is the US that has been making more money than Russia on the super-high gas prices in recent months. Thus, the value of natural gas and LNG exported by Russia in January-August 2021 was $33.197 billion, compared with $42.9 billion worth of LNG exported by the US during the same period!
Most US gas supplies to Europe come under spot contracts (at exchange prices, quick purchase and payment and delivery by a certain date) concluded in December and January, when quotations in Europe were hitting record highs. As a result, traders now supplying American gas to Europe are making super profits. In January, they not only benefited from supplying Europe with gas produced in the US, but they also diverted volumes from the Middle Eastern and even Asian routes as a result of lower gas prices in the Asia-Pacific region (APAC).
As for Gazprom, it delivers, fulfilling its contractual obligations mainly under long-term contracts, i.e. at prices significantly lower than those on the stock exchange.
If LNG supplies result in lower gas prices in Europe, that market will automatically become uninteresting to US exporters, and Europeans themselves will have to go back to buying gas from the traditional suppliers. The panic mood in Europe is therefore now being artificially maintained by allegtions that Russia could cut off gas supplies because of the escalating situation around Ukraine. It is remarkable, however, that all the LNG supplies from the US have never managed to seriously depress gas exchange quotations in Europe, while any news of successful negotiations between Russia and the US or European leaders knocks prices down by $100-150.
As we know, the European gas market is the backyard of the global LNG market, dependent on the conditions in the APAC countries, where the market is physically larger. As soon as prices begin to fall in Asia, they also fall in Europe, and vice versa. In 2021, half of US gas exports went to Asia-Pacific and only a quarter to Europe. However, the diversion of LNG flows from the US to Europe could soon result in higher gas prices in the APAC, with US gas carriers heading back to Asia and European prices again breaking records for the benefit of the same European speculators and US traders, and to the misfortune of Europeans who will pay the price for Washington’s gangster gas policy.
Europe, with its substantial gas consumption and dozens of underutilized LNG import terminals, has long been of great interest to US companies, which have spent a total of $60bn on export infrastructure. There has been a real boom in the construction of LNG terminals in Europe too, under the influence of Washington, and they have even been built in Lithuania and Poland. However, no one can deny that LNG is expensive compared to pipeline gas from Russia. This is why, until recently, Europe was very enthusiastic about buying pipeline gas cheaply from Russia and why 75-80% of Europe’s LNG terminal capacity stood empty. In any case, the main criterion for assessing the prospects of US LNG as a competitor to Gazprom in Europe is price.
However, there have been some significant deteriorations in the gas market in recent weeks. Above all, they followed Russia’s receipt in late February of written confirmation of NATO’s and the United States’ refusal to engage in a dialogue with Moscow on security guarantees. This came against a backdrop where the West had previously blatantly refused to reassure Kiev’s rampant neo-Nazi authorities, who came to power in 2014 through a Washington-inspired coup. But for 8 years, at the instigation of Washington and with the tacit support of the West, the Kiev authorities have consistently pursued a policy of genocide in Donbas, where, according to incomplete information, they have killed more than 13,000 Russian-speaking civilians and pursued a policy of Russophobia. In addition, the Kiev authorities have recently intensified their neo-Nazi activities in the country and have made increasing threats of a potential nuclear weapon capability in Ukraine, in the hope of using which Kiev has already begun to develop far-reaching plans to attack Russia.
Under these conditions and in the absence of a proper Western response to the activities of the Kiev authorities, in late February Moscow was forced to launch a special operation in Ukraine to demilitarize and denazify it for reasons of self-preservation. In response, Washington and its Western allies unleashed an information war against Russia and slapped severe sanctions. Brussels, in a bid to please the Russophobic US political establishment, has refused to certify the already built Nord Stream 2, which could have significantly eased the situation on the European gas market. However, other Russian pipelines continue to operate and pump gas to Europe. Moreover, despite the misleading anti-Russian information warfare unleashed by Washington, Russian gas continues to flow through the Ukrainian gas transmission system without interruption, as reported by the Ukrainian transmission system operator itself. Gas supplies to Europe are not just flowing through the Ukrainian pipeline, they have also increased. The Europeans have increased their requests for supply and Gazprom has begun to pump through the Ukrainian pipe all of 109 million cubic meters of gas per day instead of 50 million cubic meters per day, as it was before the Russian special operation in Ukraine began, which is a doubling of supplies.
However, due to the depletion of European underground storage facilities due to winter weather, there is almost no gas left, forcing the EU to switch to current imports, which are “obligingly” offered by the US, which itself unleashed the crisis in Ukraine to, among other things, raise the price of gas in Europe. As for the Europeans, they are so far trying to move Russia’s hydrocarbon supplies out of the sanctions bracket, although individual European politicians, such as Borel, who openly “eat from Washington’s table”, have started talking about imposing additional sanctions against Russia in the gas sector as well, to please White House policy. At the same time, such European officials know full well that Russia is not going to use its gas as a tool against Europe. The EU has no substitute for that, by the way, and many of the world’s gas exporters have already spoken out about it. And the situation in Europe will only get worse for the population if the anti-Russian policy of the current European officials continues, threatening not only the impoverishment of the population, but also the bankruptcy of many European companies and even entire sectors of the economy.
At the same time, as Europe’s anti-Russian sanctions policy continues to escalate, it cannot be ruled out that Russia may eventually, in order to ensure its own security, use hydrocarbon supplies as a retaliatory measure if it considers Western sanctions to be disastrous for the Russian economy. But such actions will only lead to a clear victory for the United States over Europe, a further increase in its dependence on Washington, including on gas, and an even greater enrichment of the United States through its previously planned increase of gas prices in Europe by exacerbating relations with Russia.
Feds Secretly Paid Media to Promote COVID Shots
By Megan Redshaw | The Defender | March 9, 2022
The Biden administration made direct payments to nearly all major corporate media outlets to deploy a $1 billion taxpayer-funded outreach campaign designed to push only positive coverage about COVID-19 vaccines and to censor any negative coverage.
Media outlets across the nation failed to disclose the federal government as the source of ads in news reports promoting the shots to their audiences.
According to a Freedom of Information Request filed by The Blaze, the U.S. Department of Health and Human Services (HHS) purchased advertising from major news outlets including ABC, CBS, NBC, Fox News, CNN and MSNBC.
HHS also ran media blitzes in major media publications including The Washington Post, Los Angeles Times, New York Post, BuzzFeed News, Newsmax and hundreds of local TV stations and newspapers across the nation.
In addition to paying news outlets to push the vaccines, the federal government bought ads on TV, radio, in print and on social media as part of a “comprehensive media campaign,” HHS documents show.
The ad campaigns were timed in conjunction with the increased availability of COVID vaccines. They featured “influencers” and “experts,” including Dr. Anthony Fauci, chief medical advisor to the White House and director of the National Institutes of Allergy and Infectious Diseases.
In March 2021, Facebook announced a social media plan to “help get people vaccinated,” and worked with the Biden administration and U.S. health agencies to suppress what it called “COVID misinformation.”
BuzzFeed News advised everyone age 65 or older, people with health conditions that put them at high risk of severe illness from COVID, healthcare workers and those at high risk of exposure to the virus to get vaccine boosters, in accordance with guidance from the Centers for Disease Control and Prevention (CDC).
Other publications, including the Los Angeles Times, featured advice from experts on how readers could convince “vaccine-hesitant people” to change their minds.
The Washington Post presented “the pro-vaccine messages people want to hear.”
Newsmax said COVID vaccines have “been demonstrated to be safe and effective” and “encouraged citizens, especially those at risk, to get immunized.”
Yet, the latest data from the CDC’s Vaccine Adverse Event Reporting System shows 1,151,450 reports of adverse events from all age groups following COVID vaccines, including 24,827 deaths since Dec. 14, 2020.
Numerous scientists and public health experts have questioned the safety and efficacy of COVID vaccines, as well as the data underlying the U.S. Food and Drug Administration’s authorization of the shots.
The media rarely covered negative news stories about COVID vaccines, and some have labeled anyone who questions the shots “science denialists” or “conspiracy theorists.”
“These outlets were collectively responsible for publishing countless articles and video segments regarding the vaccine that were nearly uniformly positive about the vaccine in terms of both its efficacy and safety,” The Blaze reported.
Congress appropriates $1 billion tax dollars to ‘strengthen vaccine confidence’
In March 2021, Congress appropriated $1 billion U.S. tax dollars for the Secretary of Health and Human Services to spend on activities to “strengthen vaccine confidence in the United States,” with $3 billion set aside for the CDC to fund “support and outreach efforts” in states through community-based organizations and trusted leaders.
HHS’s public education efforts were co-chaired by U.S. Surgeon General Dr. Vivek Murthy, former National Institutes of Health director Dr. Francis Collins, Fauci, Dr. Marcella Nunez-Smith, and CDC Director Dr. Rochelle Walensky — with Vice President Kamala Harris leading the effort from the White House.
Federal law allows HHS, acting through the CDC and other agencies, to award contracts to public and private entities to “carry out a national, evidence-based campaign to increase awareness and knowledge of the safety and effectiveness of vaccines for the prevention and control of diseases, combat misinformation about vaccines and disseminate scientific and evidence-based vaccine-related information, with the goal of increasing rates of vaccination across all ages … to reduce and eliminate vaccine-preventable diseases.”
HHS did not immediately respond to The Blaze when asked if the agency used taxpayer dollars to pay for people to be interviewed, or for a PR firm to place experts and celebrities in interviews with news outlets.
The Blaze also reached out to several news organizations whose editorial boards claimed “firewall policies” preventing advertisers from influencing news coverage, but which nevertheless took money from HHS for targeted ads.
“Advertisers pay for space to share their messages, as was the case here, and those ads are clearly labeled as such,” Shani George, vice president of communications for The Washington Post, said in a statement. “The newsroom is completely independent from the advertising department.”
Although The Washington Post may have several departments, they’re all under the authority of the same CEO and key executive team.
A spokeswoman for the Los Angeles Times said their “newsroom operates independently from advertising.”
Former Newsmax anchor confirms network paid to promote only positive coverage
According to Desert News, Emerald Robinson, an independent journalist who previously served as the chief White House correspondent for Newsmax and One America News, said she was contacted by a whistleblower inside Newsmax who confirmed the news organization’s executives agreed to take money from HHS under the Biden administration to push only positive coverage of COVID vaccines.
Robinson was also contacted by top Newsmax executives in 2021, and told to stop any negative coverage of the COVID shots as “it was problematic.”
Robinson said she was warned multiple times by executives and was told by PR experts who worked with Newsmax that medical experts or doctors likely to say negative things about COVID vaccines would not be booked as guests.
Robinson was reportedly fired by Newsmax after tweeting “conspiracy theories” about COVID vaccines and was later banned from Twitter for “repeatedly violating the platforms’ rules on COVID-19 misinformation.”
Newsmax CEO Chris Ruddy in an op-ed applauded Biden for his vaccine efforts.
Ruddy wrote:
“At Newsmax, we have strongly advocated for the public to be vaccinated. The many medical experts who have appeared on our network have been near-unanimous in support of the vaccine. I myself have gotten the Pfizer vaccine. There’s no question in my mind, countless lives would have been saved if the vaccine was available earlier.”
In other examples cited by The Blaze, “fear-based vaccine ads” from HHS featuring “survivor” stories from COVID patients who were hospitalized in intensive care units were covered by CNN and discussed on ABC’s “The View” last October.
HHS ads on YouTube featuring celebrities like Sir Michael Caine and Sir Elton John garnered millions of views.
As The Defender reported in September, a group of people injured by COVID vaccines reached out to the media to tell their stories, only to be told by news agencies they could not cover COVID vaccine injuries.
Kristi Dobbs, 40, was injured by Pfizer’s COVID vaccine. Dobbs spent months pleading with U.S. health agencies to research the neurological injuries she and others are experiencing in hopes of finding a treatment.
Dobbs said she and others who developed neurological injuries after getting a COVID vaccine shared their experiences with a reporter, in hope of raising awareness about their experiences.
Dobbs said she and others knew they needed to tell their stories, without causing “vaccine hesitancy,” to protect others from the same fate — so members of the group started writing and calling anyone who would listen, including reporters, news agencies and members of Congress.
Dobbs said they tried the best they could as simple Americans to reach out to those who would hear their stories. Finally, a reporter from a small media company was willing to do a story. Dobbs and others from the group participated in a 2-hour and 40-minute interview.
“The story never went anywhere,” Dobbs said. She said the reporter told them a “higher up” at Pfizer made a call to the station and pressured staff there into not covering any other stories about vaccine adverse reactions.
As previously reported by The Defender, the same investment firms with financial interests in Pfizer also hold large ownership stakes of corporate media outlets.
In addition, Pfizer has contracts with the federal government, which has spent billions of American tax dollars both buying COVID vaccines and promoting only positive coverage to the public.
Liberty Counsel founder and Chairman Mat Staver told Desert News, “People have been injured and died as a result of the most extensive propaganda campaign in U.S. history and it was paid for with our taxpayer dollars.”
COVID vaccines are not safe or effective, but the American public has been given propaganda by the Biden administration instead of truth from the news media, Staver said.
“The consequence is that many people have needlessly suffered as a result of the censorship and propaganda.”
Megan Redshaw is a freelance reporter for The Defender. She has a background in political science, a law degree and extensive training in natural health.
© 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
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From the Archives
A low-fat, high-carb diet has been the largest public health experiment in history. It’s past time for a rethink.
By Malcolm Kendrick | RT | November 25, 2020
New research suggests that four billion people globally will be overweight in 2050. This trend can be traced back to the ‘low-fat, high-carb’ guidelines first issued in the 70s, and should prompt a major U-turn on dietary advice.
A recent report from the Potsdam Institute predicts that by 2050 there will be four billion overweight people in the world, with one-and-a-half billion of them obese. This is not entirely surprising. The world has been getting fatter for years, and things do not seem to be slowing down.
Why is this happening? … continue
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