10 Facts From the UK Government Pfizer Vaccine Guidance that Promote “Vaccine Hesitancy”
By Johnny Vedmore |
Unlimited Hangout| December 29, 2020
Official government guidance has been released in the United Kingdom to assist healthcare professionals in administering the Pfizer/BioNTech vaccine BNT162b2. While the UK government goes to war against supposed misinformation, the official narrative is clearly based on very little to no supporting data from incomplete clinical trials. This article examines the document “Reg 174 Information for UK Healthcare Professionals” and narratives being pushed in the mainstream media that directly contradict that document.
Healthcare professionals globally have begun the controversial campaign to vaccinate large swathes of their respective populations with various experimental medical products. The vanguard of the mainstream pro-vax extremists have been busy enacting mass censorship tactics and committing blatant acts of digital book burning on a scale never before seen in the internet era. So-called “trusted sources” have become indistinguishable from the state-run media apparatus of your bog-standard dictatorship with the usual MSM outlets working non-stop to skew any information that threatens their hyper-aggressive official narrative. Throughout 2020, our basic civil liberties have been quickly stripped away by countless unelected officials from a wide array of unaccountable global power structures, all of them connected to a small group of elites who are sitting aloft the COVID-19 money train and using the heavily exaggerated epidemic to achieve their own long term goals.
Any useful data, scientific paper, or other credible research contradicting the official narrative is being purposely hidden from view. Too many uncomfortable, yet ultimately necessary, questions for vaccine companies such as Moderna, AstraZeneca, Pfizer, and their many collaborators, are being heavily censored by those pushing their own various COVID-related agendas. The promised “war on truth” is in full swing throughout all nations globally and their respective state media machines are nearly all towing their official government lines. Mainstream talk shows and podcasts worldwide are also in lockstep, and have often been caught publicly guilt-tripping their easily swayed audiences to help push them deeper into queues for mass medical trials for vaccines and other products that lack research studies on their long term effects. This inconvenient lack of completed research will not stop the money men from pumping this milky white liquid into the arms of hundreds of millions of people worldwide.
At this point in the process, the medical professionals who are administering these heavily rushed vaccines are being given the opportunity to defer responsibility and accountability for their actions to the government’s vaccine-related guidance. As the Stanley Milgram experiments have proven, when the option to defer responsibility is present, then roughly 65% of participants will follow the orders they have received regardless of the risk to their subjects. In 1974, Stanley Milgram detailed the behaviour of his participants in his famous study and suggested that people have two basic states of behaviour when they are in a social situation: “The autonomous state”, where people direct their own actions and ultimately take responsibility for the results of those actions and “the agentic state”, where people allow others to direct their actions and then pass off the responsibility for the consequences to the person giving orders, in essence acting as agents of another person’s will.
The majority of the people who are injecting these experimental drugs into their trusting patients are not likely to question the official guidance, as the overwhelming majority will often simply be in an agentic state. Thus, it should be in the best interest of anyone thinking of receiving an mRNA vaccine to first study the guidance offered by the various government sources. And, when one does study the official guidance given to healthcare professionals, one will find many different glaring contradictions and shocking admissions.
While all official bodies are attacking any inconvenient fact as misinformation, they are all busy defrauding the global population with their own misinformation campaigns that surely would have inspired awe in the likes of Joseph Stalin. So, let’s study their own words and examine the NHS guidance given to the medical professionals in the UK for the administration of the recently approved Pfizer-BioNTech vaccine.
An Introduction to Reg 174 Information for UK Healthcare Professionals (#1-4)
The short ten page official guidance being given to UK healthcare professionals contains many interesting admissions. In fact, the document, released in early December 2020 to accompany the vaccine rollout, appears to advise healthcare practitioners not to risk giving the experimental injection to the majority of the people who are due to receive the vaccine, particularly “prioritized” populations. Those in charge are pushing to vaccinate as much of the population as possible, before any critical public questions can be asked and answered, a situation that has left the safety and ethics of the vaccination campaign questionable at best and inhumane at worst.
In going through the Reg 174 document, it becomes very clear that there are many issues and recommendations that are being hidden from the general public. Here are ten of the most notable causes for concern contained within the official UK guidance document.
The authorisation to produce and supply this experimental vaccine in the UK was given by the UK Department of Health and Social Care, led by Matt Hancock – the UK Secretary of Health, and also by the Medicines & Healthcare products Regulatory Agency (MHRA). While the MHRA is part funded by the Department of Health and Social Care for the regulation of medical devices, the costs of medicine regulations are met through fees paid by the pharmaceutical industry. The agency’s financial reliance on Big Pharma has led to suggestions by some Members of the UK Parliament that the MHRA is not actually independent. Being in associated roles at the MHRA since 1985, June Raine was officially appointed as CEO in September 2019 and had previously been the Director of Vigilance and Risk Management in the Medicines Division.
2. The official Phase III safety trials will not be completed until 2023
Section 1 of the medical guidance clearly states that this vaccine guidance refers specifically to the “Pfizer/BioNTech COVID-19 mRNA Vaccine BNT162b2 concentrate for solution for injection.” On 2 December 2020, the MHRA became the first medicines regulator in history to approve an mRNA vaccine for human use, granting emergency authorisation for BioNTech and Pfizer’s BNT162b2 COVID-19 vaccine for widespread use only a week after its first Phase III eight-week trial had finished. However, the Phase III trials for BNT162b2 will not actually be fully completed until January 2023 meaning that, if you’re ready to take the vaccine now, then you should be informed that the safety trials for these experimental vaccines have at least two more years before the results are in. Regardless of that fact, Raine told reporters “no corners have been cut in approving it” and that “the benefits outweigh any risk”.
3. Will you be truly “protected” from COVID-19?
The official guidance clearly states that individuals may not be protected until at least 7 days after their second dose of the vaccine. This fact has again been ignored by various reckless pro-vax media campaigns where powerful elites such as Tony Blair have contradicted this specific recommendation, suggesting recently in an interview that people should only be given a single dose of any vaccine. Mr Blair told BBC Radio 4’s Today programme that “Does the first dose give you substantial immunity, and by that I mean over 50 percent effectiveness? If it does, there is a very strong case for not, as it were, holding back doses of the vaccine.” Blair, writing in the Independent, stated that the current vaccination strategy needed to be “altered and radically accelerated”. In responding to Blair’s call for radical acceleration, Professor Wendy Barclay, chair of virology at Imperial College London and member of the UK government’s NERVTAG, said: “I think that the issue with [Mr Blair’s suggestion] is that the vaccine is on the basis of being given in two doses, and the efficacy is on that basis.” Barclay went on to point out that “To change at that point, one would have to see a lot more analysis coming out from perhaps the clinical trial data.”
It is very important to pay attention to the wording of Reg 174 because the Pfizer vaccine purportedly boosts the immune system, rather than stopping the transmission of the virus. This would suggest that you will not be fully “protected” from COVID-19 and that you will still be able to catch the virus and could still suffer complications. The official guidance also states that “Immunocompromised persons, including individuals receiving immunosuppressant therapy, may have a diminished immune response to the vaccine,” with the guidance admitting “No data are available about concomitant use of Immunosuppressants.”
Reg 174 goes on to make this most pertinent of points when it states “As with any vaccine, vaccination with COVID-19 mRNA Vaccine BNT162b2 may not protect all vaccine recipients.” The guidance also states clearly that “administration of COVID-19 mRNA Vaccine BNT162b2 should be postponed in individuals suffering from acute severe febrile illness and that individuals receiving anticoagulant therapy or those with a bleeding disorder that would contraindicate intramuscular injection, should not be given the vaccine unless the potential benefit clearly outweighs the risk.”
4. The complicated multistage dilution and thawing process of the vaccine vials opens the major possibility of human error
In investigating the official instructions for the vaccine’s administration, we can clearly see that there are plenty of opportunities for potential human error. Section 2 of this document describes the distributed vaccine as coming in “a multidose vial and must be diluted before use.” Confirming that each vial contains 0.45 ml (which equates to 5 doses of 30 micrograms) of BNT162b2 RNA embedded in lipid nanoparticles. The delicate preparation process will be repeated 100s of millions of times globally and the multidose vial will be stored frozen and must be thawed prior to dilution. The guidance describes the process for preparing the frozen vials stating that they should be transferred to temperatures of between 2 °C to 8 °C to thaw or, alternatively, the frozen vials may also be thawed for 30 minutes at temperatures up to 25 °C for immediate use. Once thawed, the undiluted vaccine can be stored for up to 5 days at 2 °C to 8 °C, and up to 2 hours at temperatures up to 25 °C. The thawed vial must then come to room temperature and be gently inverted 10 times prior to dilution.
Some of the featured diagrams and instructions found in Reg 174
The complicated thawing and dilution process will obviously leave room for individual error. Healthcare practitioners are also warned not to shake the vials and instead to gently turn them 10 times. Prior to dilution, the vaccine should present as an off-white solution with no particulates visible. The guidance states that you must discard the vaccine if particulates or discolouration are present. The thawed vaccine must be diluted in its original vial with 1.8 mL sodium chloride 9 mg/mL (0.9%) solution for injection, using a 21 gauge or narrower needle and aseptic techniques and this complex, multistage process isn’t completed there.
The healthcare professional should then equalise vial pressure before removing the needle from the vial by withdrawing 1.8 mL of air into the empty diluent syringe. Then they should gently invert the diluted solution 10 times, again being careful not to shake the solution. The official guidance continues: “The diluted vials should be marked with the dilution date and time and stored between 2 °C to 25 °C. After dilution, the vial contains 5 doses of 0.3 mL.” The healthcare professionals are then told to “withdraw the required 0.3 mL dose of diluted vaccine using a sterile needle and syringe and discard any unused vaccine within 6 hours after dilution.”
The instructions must be followed precisely to safely administer the mRNA vaccine; there are no data available on potential consequences for the vaccine recipient if anything goes wrong during this tedious and complex multistage process. On 19 December 2020, video emerged of an official drive-thru vaccination hub which had begun operating out of a car park of Hyde Leisure Centre in Greater Manchester. The video in question, shared by No Comment TV on YouTube, shows people being vaccinated outdoors at Hyde Leisure Centre by gloveless staff and in less than sterile conditions. In an article in the Manchester Evening News four days prior to the videos release the local news site stated that “The first batch of the Pfizer/BioNTech vaccine arrives in the borough on Tuesday, with vaccinations starting at Hyde Leisure Centre on Wednesday, December 15.”
No Data Available (#5-10)
When reading Reg 174, you will soon notice a recurring theme throughout the document. The guidance clearly states on multiple occasions that there are no data available concerning some of the most important questions surrounding the mRNA vaccine. As previously noted, the actual Phase III section of the safety trials will not be completed until January 2023, meaning that two years of trials are still to be run before the vaccine can be confirmed as safe, effective and ethical.
5. The safety and efficacy of COVID-19 mRNA Vaccine BNT162b2 in children under 16 years of age have not yet been established
Although the guidance states that the safety and efficacy of the COVID-19 vaccine has not been established in children, it doesn’t mean that children have not been included within the studies. In fact, in the official Pfizer study entitled “Protocol C4591001”, one of the two main study groups included children as young as 12 years old. The inclusion of children in trials but not the guidance raises the important question, why were children included in the trial? If the vaccine is not to be given to those under the age of 16 years old, then why include children as young as 12 in the trials for an experimental vaccine technology never before authorised for use in humans?
The mainstream media, instead of raising concerns about the involvement of children in the Pfizer clinical trials, have been fully supportive of the move to test experimental pharmaceuticals on minors. CNN reported on children as young as 12 being involved in trials in an October 2020 article entitled “This 12-year-old is happy to be testing a Covid-19 vaccine” while Microsoft News recently announced that “China begins Covid test trials on children as young as age three.”
6. No data are available on the use of COVID-19 mRNA Vaccine BNT162b2 in persons that have previously received a full or partial vaccine series with another COVID-19 vaccine
We are currently witnessing the very first of many tailor-made vaccines being rolled out for general use, so don’t expect the COVID-19 jabs to be the only vaccines coming our way. With a 20 to 1 return on investment on many of these new technologies, most pharmaceutical giants will surely be lobbying governments across the globe for the next “necessary” vaccination program. The idea of multiple COVID-19 vaccinations throughout the year is already being presented as a very possible outcome for the future of humanity. Yet, no studies have been completed showing the risk of taking different types of vaccines. There have also been suggestions that people will have to have the same vaccine that they had previously taken every six months or so. This will leave Astrazeneca, Pfizer and Moderna picking up repeat vaccine contracts worth billions in secured future revenue before there are any real data on the results of the vaccines.
7. No interaction studies have been performed and there are no, or a limited amount of, data from the use of COVID-19 mRNA Vaccine BNT162b2
Admissions like these should be a cause for concern for anybody reading the official guidance. While officials and carefully chosen “trusted sources” are telling you that “no corners have been cut” in the race to approve these vaccines, it is also true that no full length studies have been completed either. These two facts are juxtaposed and obviously contradict the official narrative that is being thrust upon the general public by all of those involved.
It is clear that the officials have no real data on what will happen next and that there is a tsunami of ethical questions that are not being answered. In the absence of data, there will be speculation.
8. It is unknown whether COVID-19 mRNA Vaccine BNT162b2 is excreted in human milk and It is unknown whether COVID-19 mRNA Vaccine BNT162b2 has an impact on fertility
It is vital to note the potential dangers posed by the BNT162b2 to unborn and newborn babies as well as the reproductive organs in general. There are so many parts of the Pfizer/BioNTech clinical trials that have not yet been completed. Dr. Peter Klatsky, the Director of Fertility Preservation at the Bay Area’s Spring Fertility, talking about the coming animal trials which are to be performed over the coming months was quoted in SFGate as saying, “It will reassure me an awful lot if the protein expression is not seen on the placenta. That the mRNA isn’t making it to the placenta in animals,” he said. “I don’t expect to see any.” The article goes on to explain that it will be about another 9 months until the data has been collected and analyzed.
Section 4.6 of the official guidance recommends pregnant women should not recieve the BNT162b2 vaccine
Big names in mainstream media have also been caught recklessly promoting the vaccine to pregnant women, such as Karen Weintraub writing for USA Today, whose recent article quickly states, “Although there are very little data on how pregnant and nursing mothers will respond to a COVID-19 vaccine, professional organizations and individual doctors say the benefits are very likely to outweigh the risks.” Even though the clinical trials intentionally excluded pregnant women, Weintraub went on to state that “23 women in the Pfizer-BioNTech trial and 13 in Moderna’s became pregnant during the trial.”
While the UK’s official guidance is left sounding ambiguous, on the European continent, the European Medicines Agency (EMA) states that “the Pfizer vaccine should be considered on a case by case basis for pregnant women”, but they also reserve the right to alter the guidance if more data becomes available. It seems there is no longer any erring on the side of caution with some regulators when it comes to the COVID-19 vaccinations.
9. Non-clinical data reveal no special hazard for humans based on a conventional study of repeat dose toxicity but animal studies into potential toxicity to reproduction and development have not been completed
Animal studies have not been completed and, as referred to in the previous section, the data on those animal trials will not be available for another 9 months. It is, of course, a very rare decision to approve an experimental medical technology before any animal studies have been completed. This should be a great cause for concern for any free thinking man or woman. The fact that they have had to use what they refer to as “non-clinical” data in these studies is also in conflict with the idea that the trials were conducted to the highest professional standard. The document also fails to clearly define what non-clinical data actually means.
10. In the absence of compatibility studies, this medicinal product must not be mixed with other medicinal products
Possibly the most fascinating admission in the entire document is the absence of any compatibility studies when somebody is given the vaccine while on any other medication or medical treatment. The guidance clearly states “this medicinal product should not be mixed with other medical products.” This completely jaw dropping sentence will lead many to assume that if you are on any medication at all, then you shouldn’t be given the vaccine. Whether this refers to the mixing of other medical properties directly together with the vaccine, or simultaneous dosing of any other medical product is unclear from the official guidance.
The Mail Online and The Guardian reported in 2019 that a staggering 1 in 4 people in England – nearly 12 million people – were taking what was described as “addictive” prescription medicines such as antidepressants, sleeping pills and opioid painkillers, saying that “the NHS must take action”. Those statistics throw into question the mass rollout of a vaccination with no compatability studies. This makes the fact that elderly care home residents, followed by those aged over 80, will be the first to recieve the experimental Pfizer vaccine an extremely risky strategy. Also in 2019, Age UK reported that nearly 2 million older people were on more that 7 prescription medicines and were at “risk of side effects that are severe in some cases, and occasionally even life threatening.” This worrying issue has been barely reported by the “trusted news sources”.
A Conclusive Lack of Real Data
After examining the official guidance, one fact becomes glaringly obvious — there is little to no data on the official Pfizer vaccine in key areas. In the clinical trials, children as young as 12 years old were used as unnecessary guinea pigs. There also wasn’t enough care taken to avoid pregnant women being involved in the initial clinical trials and under the cover of unyielding and uneducated mainstream propaganda, the safety of some of the most vulnerable people involved in the vaccine trials have been ignored by Pfizer and the politicians who have successfully pushed for the public vaccination campaign to essentially replace mass clinical trials. The stage has been set for a potential disaster on an unimaginable scale. It isn’t only the participants of the trials who are risking their health for the sake of big pharmaceutical companies’ hyperinflated profit margin, but it is also the medical professionals who could be risking their futures by collaborating in these risky experimental trials, which will certainly see many people dead and irreversibly injured.
In one section of Reg 174, the Big Pharma giant lays out the risk to people’s health from the Pfizer/BioNTech vaccine. The most common adverse reaction in participants 16 years of age and older was pain at the injection site, which affected a massive 80% of those taking part in the Pfizer trials. Fatigue came a close second with 60% of trial participants becoming sluggish and tired. Half of those involved in the studies suffered from a headache as the experimental vaccine went to work while myalgia was experienced by 30% of vaccine recipients, though the results do not indicate whether the myalgia was acute (short-term) or chronic (long-term). Almost a third of participants came down with chills, while just under 1 in 5 people suffered from arthralgia (joint pain) and 1 in 10 from pyrexia (increased body temperature).
Adverse reactions reported in clinical trials are listed in the study in decreasing order of frequency and seriousness. Just under 1 in 10 people who take the vaccine will suffer from the very common and common adverse reactions referred to in the latter paragraph, such as headaches, myalgia and chills, but the more serious issues are classified as uncommon – including Lymphadenopathy (which causes swollen or enlarged lymph nodes) and nervous system disorders – which may affect up to 1 in 100 people. Rare adverse reactions that could affect up to 1 in 1000 people and very rare adverse reactions that would affect less than 1 in 10,000 of the vaccine recipients were not included in Pfizer’s self-reported safety information. It has obviously been decided that this information should be kept out of the public domain as much as possible to avoid any further vaccine hesitancy.
Not only does the official guidance actively hide the types of rare and very rare adverse effects, but they have also been leaving out some of the adverse reactions reported during the clinical trials. As I write this, the Reg 174 guidance for healthcare professionals is on version 10.1 of the document and, since its release, they have yet to admit to the potential of a certain uncommon adverse reaction to the vaccine being a specific nervous system disorder. Structural nervous system disorders include brain or spinal cord injury, Bell’s palsy, cervical spondylosis, carpal tunnel syndrome, brain or spinal cord tumors, peripheral neuropathy, and Guillain-Barré syndrome. However, previous versions of the guidance gives no clue as to what type of nervous system disorders they were referring to. However, recent articles in the USA Today, heavily promoted by the Microsoft Network, suggested that the Bell’s palsy some people came down with in the vaccine trials wasn’t related to the Pfizer jab. The article states that on Dec. 10, the FDA’s Center for Biologics Evaluation and Research held the 162nd meeting of the Vaccines and Related Biological Products Advisory Committee to discuss the emergency use authorization of the Pfizer-BioNTech COVID-19 vaccine. The USA Today piece even goes on to admit that , “a 53-page briefing noted that there had been four cases of Bell’s palsy among the vaccinated group and none among the placebo group.”
Bell’s palsy causes drooping facial muscles similar to the effects of a stroke, image source PTHealth.com
Even though Miriam Fauzia, who wrote the USA Today piece, claims that the Bell’s palsy was not related to the experimental Pfizer vaccine, the 53-page briefing she sources clearly states, “Among non-serious unsolicited adverse events, there was a numerical imbalance of four cases of Bell’s palsy in the vaccine group compared with no cases in the placebo group, though the four cases in the vaccine group do not represent a frequency above that expected in the general population.” While it is true that 1 to 4 people in 10,000 will develop Bell’s palsy within the general population, it should be noted that the 4 cases in the vaccine trials and none in the placebo group makes for a statistical anomoly that must be examined more thoroughly. Instead, the mainstream media moved quickly to discredit the Bell’s palsy links to the Pfizer vaccine using various misleading tactics to achieve their aims.
Many mainstream outlets were caught spouting the same misleading information with articles entitled “Why you shouldn’t worry about a connection between Bell’s palsy and COVID-19 vaccines,” from Business Insider and a Reuters article from 14 December 2020 entitled, “Fact check: Photo does not show three recipients of Pfizer’s COVID-19 vaccine that developed Bell’s palsy.”
In the case of the Reuters article, which is described as written by “Reuters Staff” rather than a specific journalist, the focus was not on the four Pfizer clinical trial participants who developed Bell’s palsy but instead the article discredits a random post on social media of three people with Bell’s palsy unconnected to the Pfizer vaccine. These type of misinforming mainstream media articles are commonly found to be using obvious fallacies to mislead their readership and with no individual taking responsibility for writing the misinforming piece, a trick repeated by many other media companies complicit with the official narrative. The Reuters article even goes on to admit that: “According to the FDA’s briefing document dated December 10, Bell’s palsy was reported in four vaccine participants and none in the placebo group, out of the 44,000 total participants of the late-stage vaccine trial.” However, the title of the Reuters article would mislead even some of the most keen eyed observers.
The mainstream media has been creating a flood of misleading stories, but it appears as though they have been given carte blanche to continue to do so, probably because they are sticking so tightly to the official narrative. It’s a narrative that is thick with irony, for it is the “trusted sources” who are being caught systematically misleading the general population again and again while also declaring a propaganda war against “fake news”.
The official guidance noted in Reg 174 doesn’t only highlight the serious lack of real data gained from Pfizer’s clinical trials for its Covid-19 vaccine so far, but it also exposes the wealthy medical professionals involved in these experimental vaccine development programs as complacent, reckless and very naive. It’s no secret that children are, more often than not, incapable of giving informed legal consent for such a risky and unethical enterprise. But the pro-vax extremists are using every tactic to coerce and manipulate children and their guardians into becoming human guinea pigs for Big Pharma. Pregnant women are also treated as acceptable collateral damage to advance the new science of gene, mRNA and DNA manipulation, a science and technology that pushes a sinister transhumanist agenda.
Don’t be fooled by the carefully worded vacuous celebrities, self-serving politicians, Big Pharma, and the mainstream medias authoritarian style misinformation campaigns. Keep your humanity intact and read their own words. The government guidance to healthcare professionals clearly states on multiple occasions that there are “no data available”.
Johnny Vedmore is a completely independent investigative journalist and musician from Cardiff, Wales. His work aims to expose the powerful people who are overlooked by other journalists and bring new information to his readers. If you require help, or have a tip for Johnny, then get in touch via johnnyvedmore.com or by reaching out to johnnyvedmore@gmail.com
Great Reset: Tiny Houses Pushed as Solution to Climate Change
By Paul Joseph Watson | Summit News | December 29, 2020
Social engineers are pushing tiny 200-sq-ft Ikea houses as the solution to climate change in another example of how our living standards are set to be lowered.
In an article entitled ‘Ikea tiny homes can help fight climate change by giving small footprints a big toehold’, Carl Pope, former head of the Sierra Club, gushes over the micro-homes (basically trailers) that sell for $47,550.
“Housing is an important source of climate pollution — directly responsible for about 5 percent of greenhouse gas emissions in the United States plus their electricity. Given Ikea’s emphasis on recycled and reusable materials, the company seems likely to accelerate some important shifts in the housing market. Ikea will also almost certainly take advantage of what it learns in the “tiny” segment of the building market to establish a foothold in the broader, potentially highly green, manufactured building space,” writes Pope.
While solar panels would struggle to heat larger homes, this isn’t an issue for the tiny homes, so long as you’re content living in a box.
“The use of rooftop solar panels to generate power and the replacement of propane heating with a heat pump run by those solar panels is likely to become the standard in many states for manufactured homes,” he adds. “They will gravitate toward all-electric mobile homes because propane is a significant factor in the threat of fires to mobile home parks.”
“When utopia is achieved, we will be forced to live in tiny playhouses — for our own good, because living in a rabbit hutch will improve the weather,” writes Dave Blount.
“Winter could mean praying for sunny weather so that the heat comes on. That way we will be cozy and snug when we are placed under house arrest the next time a virus comes around.”
Houses are now becoming so unaffordable for debt-stricken millennials that young people are also now literally living in decorated sewer pipes.
They’re called OPod Tube Houses and literally consist of reclaimed bits of industrial piping renovated inside with other left over pieces from building sites to make them into micro apartments.
As we previously highlighted, last year CNN promoted the idea of young people living in ‘pods’ in the center of huge cities where they have no privacy.
Rhodes Scholars Surge in Biden’s Potential Cabinet
By Matthew Ehret | Strategic Culture Foundation | December 27, 2020
With Trump’s ascension to the presidency in 2016, the Rhodes Scholars that had permeated the U.S. Deep State over many years found themselves choking on humble pie as they were removed from the drivers’ seat of world affairs for the first time in decades. The paradigm of post-nation state unipolarism that had been carefully built up over the post-WWII period had somehow been successfully challenged by an outsider as the republic was slowly returned to its patriotic traditions as a nation committed to non-interventionism, industrial progress and protectionism.
In the last few days, it has become clear that these Oxford-trained Rhodes Scholars have re-emerged as leading voices in Biden’s cabinet, and since a general understanding of this problem is so lacking today (leading many patriots to be duped into believing that the evil Chinese are at the heart of their woes), I think some preliminary words are needed as a matter of historical context.
Cecil Rhodes’ Vision Revisited
Every year since its creation in 1902, over 30 talented young American scholars have been rewarded each year with the privilege of an all-expenses paid brainwashing in the halls of Oxford University on the dime of the riches left to posterity by the deceased race patriot diamond magnate Cecil Rhodes before being re-deployed back to their home nations.
Rhodes’ early disciples included such luminaries as Lord Alfred Milner, Sir Halford Mackinder, George Parkin, W.T. Stead and the Canadian oligarch Vincent Massey (to name a few). His early backers included high level figures among the British intelligentsia including Prince Edward Albert and Lord Nathaniel Rothschild who saw that a new strategy was needed to halt the spread of American System policies around the world in the wake of Lincoln’s victory over the South during the Civil War.
At the time, anyone with half a brain knew that the unipolar days of the British Empire were coming to an end as a new multipolar system of win-win cooperation was emerging… and this was a prospect deemed intolerable by many devout social Darwinists among the British ruling class.
These early Rhodians interfaced closely with London’s Fabian Society throughout the 20th century and became the new disciplined elite that gradually infiltrated every branch of society. This new breed of imperial managers exerted its influence in much the same way earlier Jesuit operations had been formed and deployed across Europe beginning in the 16th century.
For anyone confused as to the purpose of this Rhodes Scholarship program, one need look no further than Rhodes’ 1877 Confessions of Faith and 7 wills which called for domination of the “inferior races” to Anglo-Saxon superiority, and the ultimate recapturing of America and the creation of a new Church of the British Empire:
“Let us form the same kind of society, a Church for the extension of the British Empire. A society which should have its members in every part of the British Empire working with one object and one idea we should have its members placed at our universities and our schools and should watch the English youth passing through their hands just one perhaps in every thousand would have the mind and feelings for such an object, he should be tried in every way, he should be tested whether he is endurant, possessed of eloquence, disregardful of the petty details of life, and if found to be such, then elected and bound by oath to serve for the rest of his life in his Country. He should then be supported if without means by the Society and sent to that part of the Empire where it was felt he was needed.’
In another will, Rhodes described in more detail his intention: “To and for the establishment, promotion and development of a Secret Society, the true aim and object whereof shall be for the extension of British rule throughout the world. The colonization by British subjects of all lands where the means of livelihood are attainable by energy, labour, and enterprise and especially the occupation by British settlers of the entire Continent of Africa, the Holy Land, the Valley of the Euphrates, the islands of Cyprus and Candia, the whole of South America, the islands of the Pacific not heretofore possessed by Great Britain, the whole of the Malay Archipelago, these aboard of China and Japan, [and] the ultimate recovery of the United States of America as an integral part of the British Empire.”
Describing his thinking to his disciple W.T. Stead, Rhodes wrote: “Please remember the key of my idea discussed with you is a Society, copied from the Jesuits as to organisation”.
A Calamitous 20th Century
As generations passed, the continuity of purpose that transcended individual lives of players on the stage was maintained by certain organizations that grew out of the original Rhodes/Milner Round Table movements and which had branches in every part of the Anglo-Saxon part of the British Empire. By 1919 after the Round Table had taken control of Canadian and British governments during 1911 and 1916 coups, this group created the Royal Institute for International Affairs (aka: Chatham House). By 1921, an American branch was set up called the Council on Foreign Relations (CFR) staffed with Rhodes Scholars and Fabians which has maintained a continuity of intention to the present day. This organization spawned dozens of influential sub organizations which always interface with a form of “central command”.
A young student of Harvard’s William Yandell Elliot (himself a Rhodes Scholar who operated the Oxford Branch of Harvard) was none other than Sir Henry Kissinger who stated gushingly at a May 10, 1981 Chatham House event:
“The British were so matter-of-factly helpful that they became a participant in internal American deliberations, to a degree probably never practiced between sovereign nations… In my White House incarnation then, I kept the British Foreign Office better informed and more closely engaged than I did the American State Department… It was symptomatic”.
While the Rhodes Scholar hives managed to permeate ivy league schools, media outlets, private corporations, elected offices and the civil service during the 20th century as laid out by Professor Carrol Quigley’s posthumously published The Anglo-American Establishment, the prize of the presidency remained an elusive trophy… until the day that one of Quigley’s students returned from Oxford and became Governor of Arkansas.
Clinton Opens the Floodgates
With Clinton’s 1992 presidential victory, Rhodes Scholars like Strobe Talbott (Assistant Secretary of State and co-architect of Perestroika) and Robert Reich (Secretary of Labor), were joined by Rhodies Ira Magaziner, Derek Shearer (Senior Economic Advisors), Susan Rice (Assistant Secretary of State for African Affairs), Kevin Thurme (Health and Human Services Chief of Staff), George Stephanopoulos (Communications Director) and dozens of other Rhodes Scholars. These individuals were funneled into positions of influence aiming to oversee the “end of history” celebrated by neocon thinker Francis Fukuyama as the Soviet Union disintegrated.
While some Rhodies remained in positions of power during the period of the Straussian controlled opposition of 2000-2008, the Rhodes Hives again enjoyed vast policy-shaping influence under the Obama-age where the architecture for one world government was built on the wreckage of troublesome nation states like Libya, Syria and Ukraine.
Despite the set back caused by a populist deplorable who wrestled the reins of power away from these self-professed experts in 2016, a Rhodie is a stubborn creature if nothing else, and as we have discovered in past months, both Talbott and Rice have been revealed to be two figures at the heart of the Russiagate plot designed to undo the results of 2016. While still serving as Brookings Institute President in 2015-17, it was Talbott who interfaced with MI6’s Sir Richard Dearlove and Christopher Steele in the months before the elections by cooking up and circulating the dodgy dossier and it was Rice who was revealed to be at the center of the “unmasking” entrapment operation conducted on a bewildered Michael Flynn in January 2017.
Revenge of Rice and the Rhodies
With the recently announced appointment of Susan Rice as director of Biden’s Domestic Policy Council, it has become apparent that the Rhodies are drooling at the prospect of correcting the “aberration” of Trump by re-ascending to the inner sanctum of Washington D.C., bringing in droves of Clinton-Obama era unipolar zombies with them.
Beyond Rice, other Rhodes Scholars emerging into positions of control include National Security Advisor Jake Sullivan who graduated from Oxford’s Magdalene College and worked under Strobe Talbott at the Brookings Institute’s Center for the Study for Globalization at Yale in 2000. During this time, Rice had also come to work as Senior Fellow at Brookings followed by a stint as UN Ambassador from 2009-2013 and National Security Advisor from 2013-2017, while Sullivan went onto become Biden’s top security aid during the Obama years.
Describing her love of Oxford, Rice delivered remarks at Rhodes House in 1999 saying:
“To be at Rhodes House tonight with so many friends, benefactors and mentors is a personal privilege. It is like a coming home for me for much of what I know about Africa was discovered within these walls, refined at this great university with generous support of the Rhodes Trust.”
It is worth keeping in mind that as she spoke those words, Rice had recently demonstrated her imperial worldview by coordinating the destruction of a Sudanese pharmaceutical factory in 1998 and threatening South Africa with economic destruction unless it gave up its desires for producing generic and affordable AIDS medication in the same year. Her work to carve up Sudan, promote military intervention across the Arab and African worlds under R2P and supranational organization’s like Soros’ International Criminal Court (ICC) that issued an arrest warrant for President Bashir would have made Cecil Rhodes proud. We should not forget that the Sudan-Libya-Egypt alliance under the combined leadership of Mubarak, Qadhafi and Bashir, had moved to establish a new gold-backed financing system outside of the IMF/World Bank to fund large scale development.
Pete Buttigieg
As of this writing, Rhodes Scholar Eric Garcetti (LA Mayor) has been pulled from the Biden cabinet due to a growing mountain of scandals, and corruption in his local state which have turned him into political poison for the time being.
The other Rhodes Scholar mayor Pete Buttigieg, has been more fortunate however and has been given the keys to Transport portfolio as of December 15, although had first been poised to take the position of US Ambassador to China. While many Trump supporters are being induced to hate and fear China as the “natural enemy of the USA”, it was in fact Buttigieg who demonstrated that his disdain for Trump was only paralleled by his disdain for China when he said in May 2020: “Beijing sees an opportunity to call into question the American project and liberal democracy itself. One thing they’re banking on is four more years of Trump.”
As I laid out in my previous report, Soros himself has repeatedly labelled the two greatest threats to his “open society” as 1) Xi Jinping’s China and 2) Trump’s USA.
Another Rhodie named Bruce Reed who had originally entered Washington as part of the first 1992 Rhodes Scholar infusion as the Clinton-Gore campaign manager and later director of Clinton’s Domestic Policy Council, has been tapped as the top tech advisor to Biden where he has openly called for cracking down on free speech online by cancelling Federal Internet law Section 230. This law currently keeps website owners free of prosecution for content published on their sites. It’s cancellation would crush what dwindling free speech exists on social media. The argument advanced by Reed has been that Section 230 has been used by Russian and Chinese operatives to infiltrate the information ecosystem and manipulate western elections. With its repeal, Facebook and other social media sites will be forced to censor all “illicit” thought crimes under fear of federal prosecution.
Reed had earlier teamed up with Biden in drafting the infamous 1994 crime bill which placed countless petty criminals to long-term sentences, benefiting the prison cheap labor complex. During the Obama years Reed worked as Biden’s Chief of Staff and lead handler.
Blinken, Rhodes and Soros
While Biden’s pick for Secretary of State Anthony Blinken is not himself a Rhodes Scholar, he is a life-long friend and classmate with Robert Malley (a Rhodes Scholar who had formerly acted as Special Assistant to Obama serving as “point man in the middle east” at the NSC). Earlier, Malley had been special assistant to Bill Clinton on Arab Israeli Affairs and was always deeply enmeshed with George Soros’ operations from day one of his entry into politics. Since 2016, Malley has acted as President and CEO of the International Crisis Group (ICG) founded by George Soros and Lord Malloch Brown in 1994 as a tool to promote global humanitarian wars under the guise of Responsibility to Protect (R2P). Joining Soros, Malloch-Brown and Malley at the ICG, we should not be surprised to find none other than… Jake Sullivan.
Additionally, Blinken’s father Donald Blinken made a name for himself as Soros’ point man in Hungary from 1994-1998 where he served as US Ambassador facilitating the growth of Soros’ Open Society Foundation. He was later rewarded by the Hungarian speculator with a “Donald and Vera Blinken Open Society Archive” (OSA) at Budapest’s Central European University. The Soros-funded university was created in the wake of the collapse of the Soviet Union and Blinken was instrumental in that operation.
President Viktor Orbán knew exactly what he was doing when he expelled this foreign anti-nation state brainwashing operation from Hungary’s borders in 2018. At the time, Central European University President Count Michael Ignatieff screamed “This is unprecedented. A U.S. institution has been driven out of a country that is a NATO ally.”
A Segue on Count Ignatieff
It is noteworthy that Ignatieff is himself the son of Rhodes Scholar globalist George Ignatieff and great grandson of Count Nikolai Pavlovich Ignatiev (founder of the Russian Okhrana secret police) whose family was rewarded handsomely for services rendered to London-centered oligarchy during the overthrow of the Czarist system in Russia (sort of a precursor to today’s modern Color Revolutions). This story is partially told in Cheney Revives Parvus’ Permanent War Madness by Jeff Steinberg (2005).
As a sidenote, Michael Ignatieff’s great grandfather on his maternal side is none other than George Parkin, the first controller of the Rhodes Trust from 1902-1922 and the man whose Oxford lectures and books inspired Cecil Rhodes and Milner to devote their lives to the cause of Empire. Michael is also a global board member of Soros’ Open Society Foundations headed by none other than Mark Malloch Brown (as of December 4, 2020).
As I laid out in my recent report, not only did these two upper level managers come to light as coordinators of the Dominion/Smartmatic vote fraud operation underway within the USA, but both have also pioneered the new age of regime change color revolutions beginning with Marcos’ 1986 ouster during the Peoples’ Power revolution in the Philippines, through the Balkans, Georgia, Ukraine, Kyrgyzstan, Belarus, Moldova, Bolivia, etc.
Some Final Thoughts
While the Rhodes Trust has been close to the causal nexus of much of recent world history, no one should assume that every Rhodes Scholar is guilty by association. It is an undeniable fact that some Rhodes Scholars have broken with their training and have gone on to live useful lives and I see no reason to assume, for instance, that actor/singer Kris Kristofferson played a nefarious role in anything (though some of his film choices were a bit weak).
Similarly, Canada’s John Turner did some very useful things in his short stint as Canadian Prime Minister which earned him the ire of many unipolarists then promoting NAFTA, Maastricht and the Euro. Even Bill Clinton was induced to break from his profile on a few occasions and support some good things that ran contrary to the world government agenda under the positive influence of Commerce Secretary Ron Brown (whose convenient death in 1996 alongside 34 journalists and business executives in Croatia ended that pesky issue- a story for another time).
The key thing to hold in mind is that longer waves of history are shaping the present more than most historians would care to admit. Anyone taking an intention-driven approach to historical analysis will come to recognize quickly enough that events that took place centuries ago have an active impact on the events playing out today.
How and why is this so? Because history is shaped by IDEAS. Good ideas that are in tune with the truthful nature of reality vs bad ideas that are out of tune with said reality. But this battle over ideas (and ideas about ideas e.g.: Plato’s higher hypothesis) is where the causal nexus of universal history is found. With this in mind, we can see clearly how certain people use their influence to conspire and create cultural and political institutions that transmit those ideas and organizing principles across many generations. Sometimes we find these forces to be acting in harmony with natural law (as in the case of Benjamin Franklin and his international network of co-thinkers) and sometimes very much in defiance of natural law.
Today’s battle between the opposing paradigms of the multipolar alliance led by Russia and China on the one hand vs the unipolarist/post-nation state worldview on the other has everything to do with these longer forces of history. The only way to comprehend the color revolution playing out within the USA, or the anomalous emergence of Rhodes Scholars shaping the possible Biden presidency, is by recognizing this higher reality. This exercise may cause you to think about thinking differently, and at first may be uncomfortable, but just as the figure released from the cave who slowly accustoms his/her eyes to the light of the sun and reality, the satisfaction of enjoying a higher order of truthfulness is incomparably more pleasant to a life believing in the shadows cast by an elite class of puppeteers.
Featured Video
Revive Iran’s MOU Deal or Face a Forever War /John Mearsheimer
or go to
Aletho News Archives – Video-Images
New Book
The Garlic Book — 2026
Lies are Unbekoming | November 5, 2026
What The Garlic Book shows
The book is in four parts.
Part One, The Record, treats the history of garlic as evidence. From the clay garlic bulb placed in an Egyptian grave nearly six thousand years ago, through the Ebers Papyrus, through Hippocrates, Dioscorides, Pliny and Galen, the Arab physicians under Avicenna, the medieval herbals, Culpeper, and the plague years, to the last era in which Western physicians prescribed garlic as a matter of course, which ran from 1850 to 1945. It closes with the living traditions that never stopped using it, and with the folklore of charms, vampires and the evil eye.
Part Two, The Chemistry and the Evidence, sets out what is known about why a clove has no smell until it is cut, and why the order of crush, rest and heat changes the medicine. It then reads the clinical evidence against the historical record — bacteria, blood and vessels, cancer epidemiology, metals and fatigue — and names the trials that went against garlic as directly as the trials that went for it, including the 2007 Stanford trial funded by the US National Institutes of Health which found that raw garlic, garlic powder and aged garlic extract moved LDL cholesterol no more than placebo did. It then turns to onion, garlic’s closest relative, and reads the newer evidence published since 2015, before closing with the whole of the record through the terrain lens.
Part Three, Why Medicine Set It Aside, asks the question directly. One chapter contrasts the pharmaceutical model of isolating a single active compound with the folk model of combining whole plants, and reports what the garlic evidence says about which model works better. One chapter examines the economics of research on a plant that cannot be patented. One chapter — Fire Cider — tells the story of a folk preparation whose name was taken into a United States trademark by a Massachusetts company in 2012, and won back by three herbalists in 2014 who documented forty years of prior use through Rosemary Gladstar and her students into the older tradition.
Part Four, Garlic in Practice, is the working manual — the kitchen pharmacy, traditional uses by body system, a full chapter on safety and interactions, and a complaint-by-complaint practical guide. The book closes with The Trial That Was Never Run — a one-chapter reading of the whole evidential architecture.
At the back: two appendices (a traditional list of uses, and a preparation quick-reference), a full bibliography, and a live index.
Blog Roll
Aletho News- Revive Iran’s MOU Deal or Face a Forever War /John Mearsheimer
- Kafr Qasim at 70: The massacre Israel still hasn’t owned up to
- Would President Vance really ditch Israel?
- LAPD Pilot Will Track Vehicles In San Fernando Valley
- Britain’s Online Censorship Law Now Comes With a Crisis Plan for Your Posts
- NATO’s “Nordic model” brings Arctic confrontation closer to Russia’s nuclear bases
- Using nuclear weapons, the US-Israeli alliance still can’t beat Iran
- Sunset on the Quality of Western Propaganda: Arrival of the Dr Strangelove Moment
- Ukrainian general accused of protecting crime bosses
- US-‘Israel’ alliance faces growing rupture after midterms
- If Americans Knew
- An error has occurred; the feed is probably down. Try again later.
- No Tricks Zone
- New Study: The Net Fossil Fuel Contribution To Rising Atmospheric CO2 Has Been Zero For 500 Years
- Germany’s Green Energy Transition Becoming Increasingly Expensive…Another 6 Trillion Euros!
- Sudden Stratospheric Warming, Powerful El Niño Combination May Lead To Extreme Europe Cold, Energy Crisis!
- Two New Studies Find Thwaites Glacier Melt Cannot Be Driven By Human Activity Or A Warming Ocean
- E-Cars Reduce CO2 Emissions By Only 41% Compared To Internal Combustion Engine Vehicles
- Predictions Made By Renowned Climate Professor Over Past Decades Have Been Proven To Be Poor
- New Study Suggests Large Regions Of The Pacific Ocean Have Been Cooling For The Last 80 Years
- Germany’s Green Energy Debacle: High Energy Costs Force Kahla Porzellan to Close After 182 Years!
- New Study: 50 Years Of The Most Aggressive ‘Net Zero’ Policies Can Only Affect The Global Climate By 0.03°C
- US September “Heat” Was No Record…Many Records Set Decades Ago
