WHEN the NHS suspended GP Dr Sam White without pay for daring to question the Covid narrative, they thought he would meekly disappear. Thankfully he didn’t, because the lack of debate from doctors over draconian measures the country has endured unnecessarily has been deafening. Instead, he took legal advice and his solicitor fired off a 23-page letter to the chief executive of the NHS, Sir Simon Stevens.
The colour must have drained from Stevens’s face when he opened it, even more so now as it has been made public and read over a million times. It began: ‘Please treat this letter as a public interest disclosure or whistle blow in that it raises allegations of alleged criminal conduct and breach of legal obligations by those leading the Covid response.’
It was Dr White’s viral resignation video that had angered health service chiefs. He described how he had quit as a partner from his Hampshire general practice because of the harm Covid measures were causing. He was also being prevented from using readily available effective treatments for Covid patients and he could see the toll that isolation was taking on the elderly and vulnerable. He was distraught at the thought that children would be vaccinated for a disease from which they are not at risk, whereas the experimental vaccines could cause them catastrophic damage.
All licensed doctors have a revalidation process conducted every five years either by their employer, their contracted health authority or by their governing body the General Medical Council (GMC). This is to ensure they are fit to practise and to prevent rogue doctors, such as serial killer Harold Shipman, slipping under the radar. Dr White had already passed his revalidation by the GMC without comment in December 2020, where he raised his concerns about masks, not being able to prescribe safe and effective drugs and the inaccurate PCR test. He was reassessed in April after his video made the same points, and passed again. After it went viral, however, clocking up over a million views, he was suspended in June. The NHS had had enough and the same doctor who revalidated him effectively sacked him.
Dr White’s legal letter issued by the pjhlaw legal firm accuses HM Government, the executive board of the NHS, Sage, senior members of the civil service and the executive board of the Medicines Healthcare products Regulatory Agency (MHRA) of breaching common law (derived from hundreds of years of precedent rather than recent statute) obligations, and the seven Nolan principles governing public life. The most important of these is Selflessness, meaning that decisions should be taken solely in the public interest and not for financial gain. As we have seen nine billionaires created thanks to the pandemic, alongside millions of reports worldwide of death and injury post-vaccination for a disease with a 99.7 per cent recovery rate, I think it’s safe to say they’ve trampled all over Nolan.
One of Dr White’s main complaints is that the public were not given proper informed consent before vaccination. In the pop-up vaccination hubs set up in car parks, churches and cinemas, they were not asked about their medical history. This meant if there were contra-indications to receiving the vaccine, the vaccinator did not know the jab should not be given and the vaccinated had no clue they could suffer a serious, life-changing adverse event.
The letter adds: ‘It should be noted that those presenting the information have not publicly declared at the press conferences their financial links to the vaccine industry . . . It should be noted that Moderna’s share price has risen from $10 (£7) to over $200 (£145) in the space of 18 months.
‘Bill Gates and his charitable foundation are significant investors in Moderna. Many of those presenting the information to the public are associated with or employed directly or indirectly by organisations who have been financially funded by the Gates Foundation. The MHRA, the UK regulatory body approving the vaccines, has itself been funded [£1million donation] by the Gates Foundation.’
The letter goes on to cover the unreliability of the PCR tests which are being abandoned by the US Centers for Disease Control (CDC) in December; the fact that in most fatalities patients died ‘with’ Covid rather than ‘of’ Covid; the coercive introduction of vaccine passports for travel and work, and the unnecessary use of face masks.
The NHS has offloaded Dr White’s case to the GMC, who say they have had 18 complaints from unnamed doctors offended by his resignation video, but as usual in all cases of doctors subjected to a witch hunt because they questioned the narrative, none is from a patient.
Dr White said: ‘I have received 155 pages of complaints, which is quite distressing and upsetting, and they are just downright untrue. There is one complainant alleging I used the C-word when talking about a patient, which is something I never would have done.’
The professional standards department of NHS England and NHS Improvement are struggling to find concrete evidence for his alleged misdemeanours. About the only one they can prove is that he did not wear a face mask when walking around his GP surgery (although he wore one to consult with patients) and did not advise his elderly patients to wear them because they found them distressing. Departing from NHS directives is considered unacceptable and to them, raises serious concerns regarding Dr White’s fitness to practise. Forget the fact that it’s been reported widely that face masks can do more harm than good and are nothing more than theatre.
Incidentally, coming back to Dr Harold Shipman, who murdered more than 250 patients, he was not suspended without pay. Shipman, who was arrested in 1998, kept his c£70,000 salary from West Pennine health authority even after he was convicted and jailed for killing 15 patients. He didn’t lose it until two years after his arrest, when the GMC finally struck him off. By then, his family had received more than £100,000. In contrast, the NHS has now decided, on appeal, that Dr White can receive 90 per cent of one month’s earnings from his locum work until after the GMC decide his fate.
Dr White, who is now practising functional medicine, said: ‘Complete uncertainty about my financial future is really worrying.’ He has effectively been reduced to begging for money to live on and to fight his court case against Stevens et al. Two crowd-funders are out there which he hopes will help him do both until he gets back on his feet.
https://www.crowdfunder.co.uk/dr-sams-subsistence-funds
https://www.crowdjustice.com/case/take-back-control/
July 30, 2021
Posted by aletho |
Corruption, Deception, Science and Pseudo-Science | Covid-19, COVID-19 Vaccine, Gates Foundation, NHS, UK |
Leave a comment
The forever-head of the US NIAID, Tony Fauci, has repeatedly demanded that the public “trust the science” as he shifts his own science opinion from one positon to another. What is never mentioned in mainstream media in the West or almost anywhere in the world is the scientific record of the major global vaccine making pharmaceutical giants. In short, it is abysmal and alarming in the extreme. That alone should prohibit governments from pushing radical untested experimental injections on their populations without extensive long-term animal and other testing to assure their safety.
This past April as the US vaccination program was in high gear, the Biden chief covid adviser, 80-year-old Fauci, head of the National Institute of Allergy and Infectious Disease (NIAID) since 1984, announced that the US Centers for Disease Control (CDC) and the Food and Drug Administration (FDA) had decided to order a “pause” on giving the Johnson & Johnson (Janssen) vaccine in order to examine reports of blood clots. It turned out that there were six reported blood clot cases of some seven million who then had had the J&J covid jab. Fauci in his press remarks declared, “one of the things that’s, I think, such a good thing about our system here, is that we’re ruled by the science, not by any other consideration.” There is good reason to question Fauci.
That was supposed to reassure people that the authorities were being ultra-careful with the experimental covid medications which, after all, never have been mass-tested on humans before and have only gotten “emergency use authorization,” provisional FDA approval. The FDA quickly lifted the pause as J&J agreed to print that its vaccine could cause blood clots.
Yet at the same time, rival vaccine makers, Pfizer and Moderna, both using a hyper-experimental genetic treatment known as mRNA, were not being paused by “the science” despite the fact that hundreds of thousands of alarming vaccine-related severe reactions, including official data of several thousand deaths from both, had been recorded by CDC data base, VAERS (Vaccine Adverse Event Reporting System).
According to the CDC such “adverse” events, post-vaccine, include anaphylaxis, thrombosis with thrombocytopenia syndrome, Guillain-Barre Syndrome, myocarditis, pericarditis, and death. For the week of July 16 the CDC VAERS reported an alarming 9,125 reported deaths since late December from the COVID-19 vaccinations. Never in history have such high death totals been associated with any vaccine, yet the media is deafeningly silent about this.
Their dismal science record
The wording of Fauci is precise and deliberately manipulative. It suggests that there exists some fixed thing we can call “The Science,” like some Vatican religious dogma, whereas the real scientific method is one of continuous questioning, overturning past hypotheses with newly proven ones, adjusting. Yet when it comes to “Science,” the handful of giant vaccine makers, sometimes known as Big Pharma, a cartel not unlike Big Oil, have a record of fraud, deliberate doctoring of their own tests, as well as widespread bribing of doctors and medical officials to promote their various drugs despite “Science” results that contradict their assertions of safety. A look at the major global pharmaceutical giants is instructive.
J&J
We begin with the Johnson & Johnson Company of New Jersey. On July 21, 2021 J&J and three other smaller drug makers agreed to pay a staggering $26 billion damages to a group of US states for their role in causing America’s opioid epidemic. Of that J&J will pay $5 billion. The CDC estimates that use of the highly-addictive opioids as painkillers caused at least 500,000 deaths between 1999 and 2019. Johnson & Johnson is accused of pushing the deadly painkillers for excessive use and downplaying their addiction risks. They knew better.
The same J&J is in a huge legal battle for knowingly using a carcinogen in its famous baby powder. A 2018 Reuters investigation found J&J knew for decades that asbestos, a known carcinogen, lurked in its baby powder and other cosmetic talc products. The company is reportedly considering legally splitting its baby powder division into a small separate company that would then declare bankruptcy to avoid large payouts. The J&J covid vaccine, unlike that from Pfizer and Moderna, does not use mRNA genetic alteration.
The two global covid vaccine makers which have by far the largest market to date are the two being personally promoted by Fauci. These are from Pfizer in alliance with the tiny German BioNTech company under the name Comirnaty, and from the US biotech Moderna.
Pfizer
Pfizer, one of the world’s largest vaccine makers by sales, was founded in 1849 in the USA. It also has one of the most criminal records of fraud, corruption, falsification and proven damage. A 2010 Canadian study noted, “Pfizer has been a “habitual offender,” persistently engaging in illegal and corrupt marketing practices, bribing physicians and suppressing adverse trial results.” That’s serious. Note that Pfizer has yet to make fully public details of its covid vaccine studies for external examination.
The list of Pfizer crimes has gotten longer since 2010. It is currently engaged in lawsuits related to charges its Zantac heartburn medication is contaminated with a cancer-causing substance. As well, Pfizer received the biggest drug-related fine in US history in 2009 as part of a $2.3 Billion plea deal for mis-promoting medicines Bextra and Celebrex and paying kickbacks to compliant doctors. Pfizer pleaded guilty to the felony of marketing four drugs including Bextra “with the intent to defraud or mislead.” They were forced to withdraw their arthritis painkiller Bextra in the USA and EU for causing heart attacks, strokes, and serious skin disease.
Clearly in a move to boost revenue, Pfizer illegally paid doctors kickbacks for “off-label” use of more than one of its drug which resulted in patients being injured or killed. Among them were Bextra (valdecoxib); Geodon (ziprasidone HCl), an atypical antipsychotic; Zyvox (linezolid), an antibiotic; Lyrica (pregabalin), a seizure medication; its famous Viagra (sildenafil), an erectile dysfunction drug; and Lipitor (atorvastatin), a cholesterol drug.
In another court trial, Pfizer subsidiaries were forced to pay $142 million and release company documents that showed it was illegally marketing gabapentin for off-label use. “Data revealed in a string of U.S. lawsuits indicates the drug was promoted by the drug company as a treatment for pain, migraines and bipolar disorder – even though it wasn’t effective in treating these conditions and was actually toxic in certain cases, according to the Therapeutics Initiative, an independent drug research group at the University of British Columbia. The trials forced the company to release all of its studies on the drug, including the ones it kept hidden.”
In 2004 Pfizer subsidiary Warner-Lambert was forced to pay $430 to settle criminal charges and civil liability arising from its fraudulent marketing practices with respect to Neurontin, its brand for the drug gabapentin. Originally developed for the treatment of epilepsy, Neurontin was illegally promoted off-label for the treatment of neurological pain, and in particular for migraine and bipolar disorder – even though it wasn’t effective in treating these conditions and was actually toxic in some cases. Neurontin for unapproved uses made up some 90% of the $2.7 billion in sales in 2003.
A New York Times report disclosed in 2010 that Pfizer “… paid about $20 million to 4,500 doctors and other medical professionals in the United States for consulting and speaking on its behalf in the last six months of 2009.” It paid another $15.3 million to 250 academic medical centers and other research groups for clinical trials. In the US legal practice it is seldom that corporate executives actually doing the criminal deeds are prosecuted. The result is that court fines can be treated as “business costs” in this cynical milieu. In eight years of repeated malfeasance through 2009, Pfizer accumulated just under $3 billion in fines and civil penalties, about a third of one year’s net revenues.
In 2020 as its covid vaccine was in development, Pfizer paid $13,150,000 in lobbying Congress and officials in Washington among others. Also notable is the fact that the Bill and Melinda Gates Foundation own shares of both Pfizer and their partner in the leading mRNA vaccine, BioNTech of Germany.
Moderna
The third covid vaccine producer today with FDA Emergency Use Authorization (EUA) is Moderna of Cambridge, Massachusetts. It has yet to be sued for illegal practices unlike J&J or Pfizer. But that fact is likely only because before its EUA for its mRNA experimental vaccine, in its ten years existence since 2010 it had failed to get FDA approval to market a single medicine, despite repeated failed attempts. However Moderna has a red neon sign that reads “conflict of interest” that should give pause.
Moderna and Fauci’s NIAID have collaborated on development of vaccines using Moderna’s mRNA platform and NIAID of Fauci on coronaviruses including MERS, since at least November, 2015. On January 13, 2020, before the first case of a supposed Wuhan, China “novel coronavirus” was even detected in the United States, Fauci’s NIAID and Moderna signed an updated cooperation agreement which described them as co-owners of a mRNA based coronavirus and that they had finalized a sequence for mRNA-1273, the vaccine now being given to millions for supposedly averting the novel coronavirus. That means that Fauci’s NIAID and perhaps Fauci personally (it’s allowed in the US) stood to reap huge financial benefits from emergency approval of the Moderna jab, yet Fauci has never admitted to the conflict publicly when he was Trump corona adviser, nor as Biden’s.
Ten days later on January 23, 2020 Moderna announced it was granted funding by CEPI, a vaccine fund created by Bill Gates’ foundation along with Davos WEF among others, to develop an mRNA vaccine for the Wuhan virus.
Moderna was created by a venture capitalist, Noubar Afeyan along with Harvard professor Timothy A. Springer, and others. In 2011 Afeyan recruited French businessman and former Eli Lilly executive Stephane Bancel as CEO of the new Moderna. Despite having no medical or science degree nor any experience running a drug development operation, Bancel lists himself as co-patent holder for a hundred patents of Moderna tied to the different vaccines. Beginning in 2013 the tiny Moderna was receiving grants from the Pentagon to develop its mRNA technology. As of 2020 just prior to its receiving emergency use authorization from the US Government FDA, fully 89% of Moderna revenues were from US Government grants. This is hardly an experienced company yet it holds the fate of millions in its hands. As Fauci says, “Trust the Science.”
In February 2016, an editorial in Nature magazine criticized Moderna for not publishing any peer-reviewed papers on its technology, unlike most other emerging and established biotech companies. The company remains ultra-secretive. That same year, 2016 Moderna got $20 million from the Gates Foundation for vaccine development using mRNA.
Up to its receiving EUA approval for its covid mRNA product in December 2020 Moderna had only made losses since its founding. Then curiously, following a March 2020 personal meeting with then-President Trump where Bancel told the president Moderna could have a vaccine ready in a matter of months Moderna luck changed.
On May 15, Trump announced creation of Operation Warp Seed to rollout a COVID-19 vaccine by December. The head of the Presidential group was a 30-year R&D veteran of the large UK drug firm GSK, Moncef Slaoui. In 2017 Slaoui had resigned from GSK and joined the board of none other than Moderna. Under Slaoui’s Warp Speed, some $22 billion of US taxpayer money was thrown at different vaccine makers. Moderna was a prime recipient, a brazen conflict of interest but nobody seemed to care. Slaoui funneled some $2 billion in government funds to his old company, Moderna, to develop the mRNA covid vaccine. Only under public criticism did Slaoui sell his stock in Moderna, making millions in profit from Moderna’s role as a covid vaccine leading candidate. Shortly after resigning at the end of the Trump presidency, Slaoui was fired by his old firm GSK from a company subsidiary following charges of sexual harassment of a female employee.
In February 2020 Trump Secretary of Health and Human Services, Alex Azar, invoked the Public Readiness and Emergency Preparedness Act (PREP) to exempt Moderna, Pfizer, J&J and any future covid makers from any and all liability arising from damage or death caused by their vaccines for the Wuhan coronavirus. The legal protection lasts until 2024. If the vaccines are so good and safe, why is such a measure needed? Azar was former head of the US drug giant Eli Lilly. There are some serious questions that must be raised openly regarding the vaccine makers who are now pushing experimental highly controversial gene-edited formulations in human experiments.
F. William Engdahl is strategic risk consultant and lecturer, he holds a degree in politics from Princeton University.
July 30, 2021
Posted by aletho |
Corruption, Deception, Science and Pseudo-Science, Timeless or most popular | BioNTech, COVID-19 Vaccine, Gates Foundation, Pfizer, United States |
2 Comments
It is perhaps not necessary to point out how the mainstream media in the United States as well as in Europe and Oceania persist in ignoring or otherwise covering up stories that make the Israelis look bad. Recent accounts of the slaughter of children and mostly civilians in Gaza by Israeli planes, missiles and artillery consistently try to depict the conflict as warfare between two comparable opponents, ignoring the enormous disparity in the military force available to the two sides. Israel has a modern army, air force and navy while Hamas has nothing but some small arms as well as improvised rockets and incendiary balloons.
The reluctance to criticize Israeli behavior is largely attributable to the power of the Zionist lobbies in the respective countries but it is also at least in part due to the complicity of Western governments in conniving at the Jewish state’s actions in its own region. The persistence in Israeli demands for war against Iran, preferable fought by the United States, was clear again this past week when the new government in Jerusalem declared that it would be increasing its military budget in anticipation of war with the Islamic Republic. Perhaps not surprisingly, the U.S. Congress also has several bills pending that would increase military assistance to Israel by a factor of three.
Aside from their overwhelming affection for the Jewish state, politicians and talking heads in Washington have always sought to have an enemy to explain why the foreign and national security policies have been such failures. Russia was so designated during the long years of the Cold War and more recently both the White House and Congress have begun to warn that it is China that is seeking to confront democratic norms and “export its authoritarian model.”
Given all of that, there must have been shock in a number of newsrooms when it turned out that the guilty party behind an explosive spy story that was revealed recently appears to be none other than America’s “closest ally and best friend.” It seems that a private Israeli surveillance plus security firm consisting of former cyberwarfare military and intelligence officers and having close ties to the Benjamin Netanyahu government has been selling advanced spyware to at least 45 governments. The sales are in theory restricted for use only in terrorism and criminal cases, but somehow the resource has instead been routinely used against journalists, political activists, business executives, and politicians. Saudi Arabia, for example, used the spyware to track dissident journal Jamal Khashoggi, who was murdered by Saudi agents in Istanbul in 2018.
And even though the software has been regularly used against U.S. government officials and journalists, it appears that the Biden Administration has been aware of its capabilities and has done nothing to stop it. In its own defense, the Israeli company NSO that developed the spyware has claimed, implausibly, that it can no longer be used to hack U.S. phones. That assertion was debunked by former NSA whistleblower Edward Snowden, who tweeted “NSO’s claim that it is ‘technologically impossible’ to spy on American phone numbers is a bald-faced lie: a exploit that works against Macron’s iPhone will work the same on Biden’s iPhone. Any code written to prohibit targeting a country can also be unwritten. It’s a fig leaf.”
The surprise revelation of the Israeli activity came not from a government counter-intelligence agency, but rather from a group of 17 international media organizations that formed a consortium to investigate a data leak relating to hacked telephones. The group included major news outlets that had apparently been targeted using the Pegasus hacking spyware developed by the NSO Group, which was primarily designed to penetrate the security features of smartphones. One former cybersecurity engineer from the U.S. intelligence community described Pegasus as an “eloquently nasty” tool that could be used to “spy on almost the entire world population.” The spyware “can be installed remotely on a targeted person’s smartphone without requiring them to take any action such as clicking on a link or answering a call. Once installed, it allows clients to take complete control of the device, including accessing messages from encrypted messaging apps like WhatsApp and Signal, and turning on the microphone and camera.” It can also reveal the phone’s location.
The software was designed with a backdoor which allowed NSO to monitor the surveillances and it is presumed that the information was also shared with Israeli intelligence. By one estimate 50,000 smartphones were accessed worldwide, including 10 prime ministers, three presidents including Emmanuel Macron of France, a king, foreign ministers and assorted journalists and government officials both in the U.S. and elsewhere.
A more cautious estimate from the Washington Post, which participated in the investigation, states only that “1,000 people spread across 50 different countries were identified as having numbers on the list, among them are ‘several Arab royal family members, at least 65 business executives, 85 human rights activists, 189 journalists, and more than 600 politicians and government officials.’ This includes Robert Malley, the Biden administration’s lead Iran negotiator, and journalists for CNN, the Associated Press, the Wall Street Journal, and the New York Times.” Other news agencies that were hacked by Pegasus include Agence France-Presse, Al Jazeera, France 24, Radio Free Europe, Mediapart, El País, the Associated Press, Le Monde, Bloomberg, the Economist, Reuters and Voice of America.
Some are inevitably wondering why the Biden White House has been silent about NSO. It has not identified the Israeli firm as a threat to national security and made demands to the Israeli government that it intercede with NSO and shut down the use of Pegasus until some international regulation of the use of hacking software can be developed. Part of the explanation for the reluctance might be that Biden’s senior adviser Anita Dunn’s consulting firm SKDKickerbocker was hired by NSO in 2019 to provide “public relations” advice to improve the company’s image.
The reluctance, of course, also derives from the fact that Israel is involved, but those with longer memories of the Jewish state’s record in stealing American secrets should not be surprised by this latest venture. Israeli-recruited U.S. Navy analyst Jonathan Pollard was, for example, the most damaging spy in U.S. history. And Israel has, in fact, a long history of stealing U.S. technology and military secrets to include sharing them with countries that Washington has regarded as enemies, including China and Russia.
Israel always features prominently in the annual FBI report called Foreign Economic Collection and Industrial Espionage. The 2005 report states: “Israel has an active program to gather proprietary information within the United States, these collection activities are primarily directed at obtaining information on military systems and advanced computing applications that can be used in Israel’s sizeable armaments industry.” It adds that: “Israel recruits spies, uses electronic methods, and carries out computer intrusion to gain the information.” A 1996 Defense Investigative Service report noted that: “Israel has great success stealing technology by exploiting the numerous co-production projects that it has with the Pentagon.” It says: “Placing Israeli nationals in key industries is a technique utilized with great success.” A General Accounting Office (GAO) examination of espionage directed against American defense and security industries described how: “Israeli citizens residing in the U.S. had stolen sensitive technology to manufacture artillery gun tubes, obtain classified plans for reconnaissance systems, and pass sensitive aerospace designs to unauthorized users.” The GAO concluded that: “Israel conducts,” and this is a quote, “conducts the most aggressive espionage operation against the United States of any U.S. ally.” More recently, FBI counterintelligence officer John Cole has reported how many cases of Israeli espionage are dropped under orders from the Justice Department. He has provided a conservative estimate of 125 viable investigations into Israeli espionage — involving both American citizens and Israelis — that were stopped due to political pressure.
So Israel gets yet another pass on its spying against the United States. Indeed, the Biden Administration has yet to definitively comment on the latest impropriety. One wonders when the penny will drop and the American people will rise up and say “enough is enough.”
July 29, 2021
Posted by aletho |
Corruption, Deception, Ethnic Cleansing, Racism, Zionism | Israel, NSO Group, United States, Zionism |
3 Comments
The National Institutes for Health (NIH) is exceptionally keen on the study of “Long Covid.” The federal agency recently allocated over $1 billion in funding for this purpose, and NIH Director Francis Collins has made the claimed ailment a recurring subject of his press commentary over the last year. The Department of Health and Human Services similarly signaled that it intends to classify “Long Covid” as a recognized disability for government funding and classification purposes.
So what is Long Covid, and why is it drawing so much attention and funding out of the federal government? As with any respiratory illness, Covid-19 does appear to have long-term sufferers who do not follow the normal recovery pattern and continue to demonstrate symptoms for weeks or months after an infection. At the same time however, the push to make “Long Covid” a distinctive medical classification unto itself appears to be a political phenomenon, wrapped up in clear signs of pseudoscience and linked back to a fringe “alternative wellness” blog that originally coined the term in March 2020.
A recent study published in the Lancet-owned journal EClinicalMedicine purported to document over 200 symptoms of Long Covid, ranging from fairly common Covid-19 ailments such as fatigue, cough, or long-term loss of smell to an eclectic assortment of problems such as hallucination, brain fog, tearfulness, insomnia, and mood anxiety. Media reports breathlessly repeated these findings to press the urgency of funding for Long Covid research, while also hyping the syndrome as a further justification for alarmism in justifying lockdowns and similar measures. After all, if Long Covid afflicts a sizable subset of Covid patients – as some claim – and can strike young people who are at a much lower mortality risk from the virus itself, then perhaps more restrictive measures are warranted on the general population – or so the argument goes.
Many lockdown advocates have seized onto the Long Covid narrative, incorporating it into their defenses of the draconian non-pharmaceutical interventions they have advocated over the last year and a half. The CovidFAQ website – a UK-based project set up by “neoliberal” activist Sam Bowman and British MP Neil O’Brien – invokes the threat of Long Covid in its attacks the Great Barrington Declaration (GBD), arguing that the hypothesized syndrome undermines evidence that the virus is substantially less-severe among younger demographics. Several pro-lockdown scientists and epidemiologists issued coordinated statements attacking the GBD in October 2020 for “ignor[ing] the emerging burdens of long COVID.” These statements are usually offered as declarative assessments, treating Long Covid as an established medical fact.
With billion-dollar budgets and the prospect of additional sweeping policy measures at stake, it only makes sense to ask if the science behind Long Covid is sound. There is no doubt that some Covid-19 victims have symptoms that linger for weeks or months beyond the typical recovery, although that is true of many diseases. Whether it has 200 plus symptoms is another story – and a closer look reveals an alarming amount of outright quackery is currently shaping the scientific and media discourse around Long Covid.
The problem arises from the amorphous definition of the phrase “Long Covid” itself. Far from a careful clinical diagnosis, Long Covid has become a catch-all term for any extended medical ailment, real or imagined, attributed to the effects of the Covid-19 virus. An alarming amount of alleged data about the phenomenon traces back to a single source called the “Body Politic Wellness Collective” – an alternative medicine blog with dubious scientific credentials. To quote one recent study of the term’s origins, “the emergence and recognition of Long COVID as a potentially major public health problem is largely due to advocacy groups such as the Body Politic COVID-19 Support Group, and Patient Led Research For COVID-19” – the latter an affiliated survey administrator that, according to its own website, was “born out of the Body Politic Slack support group.”
The same Body Politic group frequently appears in an already large and growing literature on “Long Covid” in other scientific journals. In September 2020, NIH Director Collins devoted his personal column on the agency’s website to touting the group. He later credited their work when launching the aforementioned $1 billion research initiative. In July 2021, Body Politic reappeared at the center of the aforementioned EClinicalMedicine study along with a spinoff organization called the Patient-Led Research Collaborative. The two groups administered the survey behind the claim that Long Covid carries over 200 symptoms.
Before we get into the survey itself, it’s useful to take a closer look at the Body Politic group. TheWall Street Journal recently ran a lengthy expose of the organization by Jeremy Devine, an Ontario-based psychiatrist. Devine found that the group’s initiatives sprang to life at the outset of the pandemic in March 2020. They first coined the Long Covid moniker around this time, promoting it in a flurry of media appearances. In early April, the New York Times ran an op-Ed by Body Politic’s co-founder calling attention to the syndrome and recounting her own experience as a “long hauler” (which, at the time, consisted of experiencing symptoms for about three weeks after testing positive).
As Devine documented in the WSJ, the Body Politic group’s approach to scientific survey design appeared highly unorthodox. It frequently relied on self-reported descriptions of Long Covid symptoms, instead of independent medical verification. It also had a habit of diagnosing people with Long Covid even after they tested negative for Covid-19 itself. A March 2021 report by Adam Gaffney for StatNews called attention to similar problems with Body Politic’s research design. “[A]t least some people who identify themselves as having long Covid appear never to have been infected with the SARS-CoV-2 virus,” Gaffney noted. They were nonetheless touted by the media as case studies in the alleged syndrome.
A closer look at the Body Politic group itself raises several red flags about their scientific qualifications. The group’s executive board boasts few, if any, actual medical practitioners or scientific experts. Instead we find an eclectic assortment of political activists, musicians, poets, and journalists, many of whom share common interests in “alternative medicine.” Body Politic’s Treasurer and principle support group organizer describes herself as a “practicing Spiritual Medium” who specializes in detecting “invisible illness.” The website’s Vice President is a “social & racial justice activist,” and its Secretary is an “aspiring sex coach.” Other affiliates include a self-described “socialist poet,” multiple “social justice activists,” and people who describe their careers as operating at the intersection between art and natural wellness. The group’s website and social media accounts frequently invoke political terminology from the critical theory literature. They describe themselves as “a queer feminist wellness collective and a space for inclusivity, accessibility, and crucial discussions about the very real connection between wellness, politics, and personal identity.” Their values statement espouses “patient-led” research to “democratize” medicine – descriptions that appear to forgo traditional scientific methods of testing and verification in favor of placing heavier reliance on patient testimonials and personal experience.
While the group’s activism alone does not disqualify their commentary, the unconventional qualifications of its leadership should raise suspicion about their claimed expertise on Long Covid. When NIH Director Collins personally promotes Body Politic’s work, he is creating a false sense of scientific credibility around their work. Few who read Collins’s statements are aware that the group he praises as “citizen scientists” might be better characterized as an odd assortment of psychic healers, magic crystal gurus, and alternative medicine activists. As a leading public health official, Collins’s many endorsements of this quackery border on irresponsible.
Turning to Body Politic’s survey projects, we quickly find that skepticism of their credibility is warranted. The group’s survey design specifically eschews requiring a positive Covid-19 test or antibody test to confirm that their respondents actually had the disease. “[W]e do not believe people’s experiences with COVID-19 symptoms should be discounted because they did not receive a positive test result,” states one justification for this unconventional data collection procedure. To qualify as a sufferer of Long Covid, it seems, a person needs only to claim that he or she suffers from Long Covid. Lived experience of the disease trumps any requirement of scientific verification.
The prevalence of unverified and untested Covid claimants being classified nonetheless as Long Covid sufferers is stunning. In the WSJ, Devine reports the numbers from the group’s first survey, administered through their website in 2020: “Nearly half (47.8%)” of Body Politic’s survey respondents “never had testing and 27.5% tested negative for Covid-19. Body Politic publicized the results of a larger, second survey in December 2020. Of the 3,762 respondents, a mere 600, or 15.9%, had tested positive for the virus at any time.” As Gaffney notes in StatNews, this practice raises the distinct possibility that survey respondents are misattributing other chronic symptoms to the virus.
Their new study in the Lancet’s journal EClinical Medicine does not offer much hope that Body Politic has improved its survey design. Its authors state that “We analyzed responses from 3762 participants with confirmed (diagnostic/antibody positive; 1020) or suspected (diagnostic/antibody negative or untested; 2742) COVID-19, from 56 countries.” Unconfirmed Covid patients with self-reported Long Covid symptoms outnumber confirmed Covid patients by almost 2.7 to 1. To their credit, the group discloses the lack of PCR or antibody testing confirmation among the majority of their respondents. The extremely high rates of unconfirmed cases, however, are more than sufficient to cast doubt upon their claims to have identified over 200 separate Long Covid symptoms.
The survey’s design also appears to self-select for people who are inclined to claim Long Covid symptoms, whether valid or not. According to the paper, the survey consisted of 257 questions, took almost 70 minutes on average to complete, allowed participants to revisit their answers for up to 30 days, and was primarily marketed to readers of the Body Politic group’s various blogs and Slack channels. This design practically ensures that the majority of the people who received and completed the survey were drawn from a readership that already gravitates towards the group’s political messaging and medical eccentricities.
Imagine if a survey on diet products collected its sample entirely from the mailing list of Gwyneth Paltrow’s “Goop” store. And imagine if the CDC decided to use that survey as a basis for a billion dollar program to revise its food nutrition guidelines, claiming that it is a representative study of the average American’s diet. Because that’s essentially what NIH Director Francis Collins has done with Body Politic’s surveys when justifying his current research initiative into Long Covid before the public.
With most Long Covid research at the moment, self-diagnosis by amateur groups appears to have supplanted scientific rigor in driving the NIH’s research priorities. Even minimal scrutiny should cast doubt upon the Body Politic group’s deficit of scientific credentials and surplus of outright “alternative medicine” quackery. Yet in January 2021 the New York Times heavily leaned on testimonials from Body Politic’s resident psychics and alternative wellness healers in a feature story on so-called Long Covid, aiming to demonstrate the scientific validity of the diagnosis.
So did an August 2020 piece in the Atlantic that is widely credited with popularizing the concept. Indeed, the New York Times has turned its opinion page over to Body Politic writers on multiple occasions over the last year, giving them free rein to promote unscientific claims about the concept. Simply scanning over mainstream media coverage of “Long Covid” in the last year reveals that Body Politic-affiliated activists with dubious scientific credentials have become go-to “experts” on the subject. Here they are being interviewed in Vox, in the Guardian, in the Washington Post, on NPR, in Buzzfeed, and on MSNBC.
In calling attention to Body Politic’s influence over shaping the Long Covid narrative, I do not question the possibility that some of the organization’s activists may exhibit genuine long-term Covid-related symptoms, even if they are not a distinct classification unto itself. But scientific assessment of their claims remains woefully inadequate relative to the authority that the media has bestowed upon them. In this sense, much of the Long Covid literature bears striking resemblance to other claimed chronic illnesses that have less-than-robust scientific grounding (for example, consider the difference between Celiac disease – a rare but severe dietary illness involving gluten – and the mid-2010s “gluten sensitivity” craze, which mixed together real and imagined but also self-diagnosed symptoms, fad dietary practices, and dubious scientific attestation)
Despite their scientific shortcomings, Body Politic’s own surveys have found a welcome audience among many academics who should know better. Even leading medical journals now regularly tout Body Politic’s dubious survey results as if they are scientific fact.
Last fall, the BMJ published an article on “Long Covid” from a team of scientists led by Oxford’s Trisha Greenhalgh, an outspoken pro-lockdown regular on the BBC and other UK media circuits. Greenhalgh’s team estimated that perhaps as many as 10% of people infected with Covid develop “Long Covid” symptoms – a number that has since become a standard estimate for Long Covid risks.
Their empirical “evidence” for Greenhalgh’s claim, in turn, derives primarily from Body Politic’s “patient-led survey” of alleged Long Covid sufferers – the same survey where half or more of respondents never even had a confirmed Covid diagnosis. This was no accidental reliance on a substandard source, deriving from insufficient scrutiny of the survey’s methods. Greenhalgh credited the Body Politic group by name on Twitter for inspiring their paper, endorsing the “lived experience” of their “patient-led research.” Echoing the Body Politic survey, Greenhalgh and her co-authors further embrace the proposition “that a positive test for covid-19 is not a prerequisite for diagnosis” for Long Covid. It’s apparently sufficient to simply believe that you had a prior bout with Covid, and attribute your claimed long-term symptoms to the same.
Not surprisingly, Long Covid has become a favored fallback argument among lockdowner epidemiologists to argue for prolonged restrictions. Duke University’s Gavin Yamey has made a name for himself by credulously circulating conspiracy theories about the Great Barrington Declaration by blogger Nafeez Ahmed. Sure enough, he’s also a Long Covid activist, promoting Greenhalgh’s study as well as an assortment of news articles that blur the lines between legitimate reporting of long-term symptoms and quackery.
Although Body Politic is far from the only group advocating for Long Covid research funding, their high-profile promotion by the NIH, by leading news outlets, and by medical journals suggests a similar phenomenon to the pattern seen among other lockdown advocates in allegedly-mainstream epidemiology. We’re witnessing a full-scale breakdown of the screening mechanisms that normally steer scientific discourse away from fringe and conspiracist viewpoints – provided that those viewpoints may be used to advance the alarmist ideologies that have emerged around Covid policy over the last year. The doors have, sadly, been thrown wide open to psychic healing and alternative wellness gibberish. Lockdowner scientists have, in turn, given these suspect claims and defective survey designs a welcome home in the most prestigious institutions of journalism, government, and the ivory tower.
Phillip W. Magness is a Senior Research Fellow at the American Institute for Economic Research. He holds a PhD and MPP from George Mason University’s School of Public Policy, and a BA from the University of St. Thomas (Houston).
Prior to joining AIER, Dr. Magness spent over a decade teaching public policy, economics, and international trade at institutions including American University, George Mason University, and Berry College.
July 27, 2021
Posted by aletho |
Corruption, Deception, Mainstream Media, Warmongering, Science and Pseudo-Science | Covid-19, NIH, United States |
1 Comment

It is simply no longer possible to believe much of the clinical research that is published, or to rely on the judgement of trusted physicians or authoritative medical guidelines. I take no pleasure in this conclusion, which I reached slowly and reluctantly over my two decades as an editor of the New England Journal of Medicine.
Marcia Angell
Check out this image from a peer reviewed research paper that supposedly shows skin lesions being treated by a laser:

Left: before treatment for keratoses. Right: after they were airbrushed out. (image diff is available here)
On being challenged the authors said:
The photograph was taken in the same room with a similar environment; unfortunately the patient wore the same shirt.
The journal found this explanation acceptable and forwarded the response to the complainants.
It’s becoming clear that science has major difficulties with not only a flood of incorrect and intellectually fraudulent claims, but also literally faked, entirely made up papers with random data, imaginary experiments and photoshopped images in them. Some of these papers are sold by organised gangs to Chinese doctors who need them to get promoted. But others come from really sketchy outfits like (sigh) the National Health Service, to whom we owe the masterpiece seen above.
The British Government hasn’t noticed that its doctors are massaging medical evidence. Instead this example comes from Elizabeth Bik, who runs a blog where she and a few other volunteers try to spot clusters of fraudulent papers. She embarrassed the journal in public here, and the paper was finally retracted. But she’s just a volunteer who raises money on Patreon for her work. Here’s her assessment of what’s going on:
Science has a huge problem: 100s (1000s?) of science papers with obvious photoshops that have been reported, but that are all swept under the proverbial rug, with no action or only an author-friendly correction… There are dozens of examples where journals rather accept a clean (better photoshopped?) figure redo than asking the authors for a thorough explanation.
As the only people trying to spot these fake papers are bloggers, we can safely assume that far larger numbers of papers are fake than the “thousands” they have already found and reported. For example,
0.04% of papers are retracted. At least 1.9% of papers have duplicate images “suggestive of deliberate manipulation”. About 2.5% of scientists admit to fraud, and they estimate that 10% of other scientists have committed fraud.

It’s been known for years that a lot of claims made by scientists can’t be replicated. In some fields, the majority of all claims appear to not replicate due to a large mix of issues like overly lax thresholds for claiming statistical significance, poor study design and other somewhat subtle errors. But how much research is deliberate falsehood?
The sad truth is the size of the fraud problem is entirely unknown because the institutions of science have absolutely no mechanisms to detect bad behaviour whatsoever. Academia is dominated by (and largely originated) the same ideology calling for the total defunding of the police, so no surprise that they just assume everyone has absolute integrity all the time: research claims are constantly accepted at face value even when obviously nonsensical or fake. Deceptive research sails through peer review, gets published, cited and then incorporated into decision making. There are no rules and it’d be pointless to make any because there’s nobody to enforce them: universities are notorious for solidly defending fraudulent professors.
So let’s turn over the rock and see what crawls out. We’ll start with China and then turn our attention back to more western types of deception.
Chinese fraud studios
In 2018, the U.S. National Science Foundation announced that: “For the first time, China has overtaken the United States in terms of the total number of science publications.” Should the USA worry about this? Perhaps not. After some bloggers exposed an industrial research-faking operation that had generated at least 600 papers about experiments that never happened, a Chinese doctor reached out to beg for mercy:
Hello teacher, yesterday you disclosed that there were some doctors having fraudulent pictures in their papers. This has raised attention. As one of these doctors, I kindly ask you to please leave us alone as soon as possible… Without papers, you don’t get promotion; without a promotion, you can hardly feed your family… You expose us but there are thousands of other people doing the same. As long as the system remains the same and the rules of the game remain the same, similar acts of faking data are for sure to go on. This time you exposed us, probably costing us our job. For the sake of Chinese doctors as a whole, especially for us young doctors, please be considerate. We really have no choice, please!
Note the belief that “thousands of other people” are doing the same, and that these doctors need more than one paper to keep being promoted, so the 600 found so far is surely the tip of an iceberg given China’s size. There are about 3.8 million doctors in China implying that there are quite possibly tens of thousands, maybe hundreds of thousands of these things in circulation.
The fake papers are remarkable:
- They are so good they are undetectable in isolation. The NHS photo is an aberration – normally these papers get spotted by noticing re-used technical images across papers that claim to be different experiments by different people. The fake papers are probably produced by real scientists with access to real lab equipment. The use of spammy-looking Gmail accounts is also a signal because Gmail is banned in China (e.g.
BrendaWillingham12192@gmail.com, RosettajKirkland3814@gmail.com, CaseyPeiffer8311@gmail.com). The reliance on bot-generated Gmail accounts implies enormous scale.
- They are peer reviewed and published in western journals. For instance, the Journal of Cellular Biochemistry by Wiley or Biomedicine & Pharmacotherapy by Elsevier. They claim to be doing advanced micro-biology on serious diseases: a typical title is something like “MicroRNA-125b promotes neurons cell apoptosis and Tau phosphorylation in Alzheimer’s disease”. Journals have no way to detect these papers and aren’t trying to develop any.
- Some of them present traditional Chinese medicine as scientific. TCM is more or less the Chinese equivalent of homeopathy with lots of herbal remedies, eating body parts of exotic animals to cure erectile dysfunction, and so on. But the Chinese Government is obsessed with it and thinks it’s the same as normal medicine. From the top down, Chinese scientists are expected to produce papers claiming that TCM works, and they do! Mostly this stuff stays in Chinese but the ever increasing reliance of western universities on Chinese funding means it’s now finding its way into the English language literature as well, e.g. “Probing the Qi of traditional Chinese herbal medicines by the biological synthesis of nano-Au” was published by the Royal Society of Chemistry.

Advert by a research faking operation. Credit to “Smut Clyde” and “TigerBB8”.
Most western scientists are too clever to buy a completely fake paper (or so we hope). But their promotion incentives are identical, and there are other techniques that let you publish as many fake papers as you want. Let’s turn our attention to…
Impossible numbers in western science
The case against science is straightforward: much of the scientific literature, perhaps half, may simply be untrue.
Richard Horton, editor of the Lancet
How many scientists just make up their data? A well known recent case of this was the Surgisphere scandal, in which a paper appeared in The Lancet that claimed to be based on a proprietary dataset of nearly 100,000 COVID-19 patients across over 670 U.S. hospitals. This figure was larger than the official case counts of some entire continents at the time, and there was no reason for hospitals to share tightly controlled medical data with a random company nobody had heard of, so the claim was implausible on its face. Sure enough, when challenged it turned out none of the authors had ever actually seen the data, just summaries of it provided by one guy, who on investigation had a long track record of dishonesty. The Lancet probably accepted this paper because it made Trump look bad and the editor (Horton, quoted above) appears to hate Trump more than he hates bad science.
There are some other cases like this that came to light over the years, like the story of Brian Wansink, or that of Paolo Macchiarini, who left a trail of dead patients in his wake. But while anecdotes about individual cases are interesting, can we be more rigorous?
One clue comes from automated tools that scan research papers looking for mathematically impossible numbers, which can sometimes be detected even in the absence of the raw original data. In recent years a few such tools have been developed and deployed, mostly against psychology and food science.
Being flagged by a stats checker doesn’t guarantee the data is made up: GRIM can detect simple mistakes like typos and SPRITE requires common sense to detect that something is wrong (i.e., no child will eat a plate of 60 carrots). But when there are multiple such problems in a single paper, things start to look more suspicious. The fact that half of all papers had incorrect data in them is concerning, especially because it seems to match Richard Horton’s intuitive guess at how much science is simply untrue. And the GRIM paper revealed a deeper problem: more than half of the scientists refused to provide the raw data for further checking, even though they had agreed to share it as a condition of being published. This is rather suspicious.
One of the difficulties with detecting scientific fraud is that the line between dishonesty and simple absurdity can get quite blurry. Sometimes scientists “calculate” data that is clearly wrong, but don’t actually try to hide or it may even admit to it in the paper, knowing full well that nobody cares and nonsensical data won’t actually matter. Here’s an example from a COVID modelling paper:

The model was allowed to calculate that the average Brit must live with 7 other people, because it couldn’t obtain data fit otherwise (actual number=2.4). This one comes from University College London, is written by 12 neuroscientists, passed peer review and has 37 citations. The peer reviewer noticed that the incorrect number was in the paper but signed off on it anyway.
For decades psychiatrists published research into the “gene for depression” 5-HTTLPR. They created an entire literature not only linking the gene to depression but explaining how it worked, linking it to parenting styles, developing treatments based up on it. Over 450 papers were published on the topic. Eventually a geneticist discovered what they were doing and used DNA databanks to point out that none of those papers could possibly be true.
Sometimes numbers aren’t “wrong” but are instead logically vacuous. The Flaxman et al paper from Imperial College that tried to prove lockdowns work had the usual problem of statistically implausible numbers, but more importantly was built on circular logic: their model assumed only government interventions could end epidemics. This is obviously nonsense and they breezily admitted it in the paper, where they said their work was “illustrative only” and that “in reality even in the absence of government interventions we would expect Rt to decrease”. No problem: this fictional illustration got published in Nature and the authors presented the model’s outputs as scientific proof of their own assumption to the media. The paper is vacuous mathematical obfuscation, but scientists either can’t tell or don’t care: it has racked up over 1,300 citations and the number is still growing rapidly. To put that number in perspective, in physics the top 1% of all researchers have around 2,000 citations over their entire career.
Time to assume that health research is fraudulent until proven otherwise?
Earlier this month, the BMJ published an astounding blog post with the same title as this section. There’s no need to add anything because simply quoting it is sufficient:
The anaesthetist John Carlisle analysed 526 trials submitted to Anaesthesia and found that… when he was able to examine individual patient data in 153 studies, 67 (44%) had untrustworthy data and 40 (26%) were zombie trials… [Ben] Mol’s best guess is that about 20% of trials are false. Very few of these papers are retracted.
We have now reached a point where those doing systematic reviews must start by assuming that a study is fraudulent until they can have some evidence to the contrary.
Richard Smith
Richard Smith is a former editor of the BMJ, cofounder of the Committee on Medical Ethics (COPE), for many years the chair of the Cochrane Library Oversight Committee, and a member of the board of the U.K. Research Integrity Office.
Or put another way, an overseer of the Research Integrity Office believes research has no integrity.
What can be done?
600 fraudulent papers here, 450 over there, 1300+ citations of just one bad paper… pretty quickly it starts adding up.
We’re often told science is self-correcting. Is that true? Probably not. “The Science Reform Brain Drain” is perhaps the bleakest essay I’ve read this year. Reformers like the men who developed SPRITE and GRIM have been giving up and leaving science entirely. Pointing out in public that your colleagues are dishonest is never a great career move, and the work was often futile. One scientist who quit and went into industry summed up his fraud detection work like this:
The clearest consequence of my actions has been that Zhang has gotten better at publishing. Every time I reported an irregularity with his data, his next article would not feature that irregularity.
Even when a bull enters the China shop and gets a few papers retracted, it doesn’t actually matter because it has little effect: retracted papers keep getting cited for years afterwards and actually may be cited more than non-retracted papers, because one of the effects of retraction is that the article becomes free to download.
In the past year most talk of bad science has been about models with bad assumptions. This is an issue but has been hiding problems that are far worse: scientists are buying fake papers, Photoshopping evidence, refusing to upload their data, knowingly publishing numbers that cannot be correct, citing papers that were retracted for being fraudulent and (of course) presenting mathematical obfuscations of what they want to be true as if it were science. Journals usually ignore fraud reports entirely, or when put under pressure let scientists submit “corrected” versions of their papers. And worst of all, the journal editors that are responsible for scientific gatekeeping know all this is happening, but aren’t doing anything about it.
In fact, very little can be done because above all, universities rely on reputation and don’t want anyone to find out about bad behaviour, so they fight tooth and nail to protect academics no matter how badly they are behaving. There are no rules. Any rules that are alleged to exist turn out when tested to be illusions.
Claims made by scientists are automatically trusted by the majority of people. Maybe they shouldn’t be?
Mike Hearn is a former Google software engineer. You can read his blog at Plan 99.
July 22, 2021
Posted by aletho |
Corruption, Deception, Science and Pseudo-Science, Timeless or most popular |
1 Comment
Chilling new proposals
As if there needed to be yet another threat to free speech in the UK, British journalists could face 14-year prison sentences for publishing stories embarrassing the government, under proposed reforms to the Official Secrets Act. According to the government, the new proposals will crack down on foreign spies but many fear it could even be used domestically.
The UK government, through the Home Office, has proposed reforms to the 1989 Official Secrets Act, to account for changes technology and the internet has enabled in the sharing of leaked data.
But critics have noted that with the proposed changes local journalists are not protected if charged under the new laws.
Critics further noted that if the new proposals were currently law, the journalists who revealed that former Health Secretary Matt Hancock broke his own COVID rules while having an affair with his aide would have been charged. The leak was newsworthy and the story broke through leaked CCTV footage.
Last week, the Information Commissioner’s Office came under fire when it emerged that it searched two homes while investigating how the CCTV footage leaked to The Sun, the news outlet that first broke Matt Hancock’s affair story.
Among the groups criticizing the new proposals is the National Union of Journalists (NUJ), which noted that the new law would treat whistleblowers and those who publish leaked content the same way foreign spies are treated.
A spokesperson for the organization said:
“Existing legislation distinguishes provisions and penalties between those who leak or whistleblow, those who receive leaked information, and foreign spies.
“The government proposes to eliminate or blur these distinctions. The government also wants to increase the maximum penalties that journalists might suffer for receiving leaked material from two to 14 years…
“The NUJ has long argued that where whistleblowers believe that they have acted in the public interest, they should be able to make this case in court, and if a jury agrees with them, be protected.”
But according to the Home Office:
“Since the passage of the Act in 1989, there have been unprecedented developments in communications technology (including data storage and rapid data transfer tools) which in our view, means that unauthorized disclosures are now capable of causing far more serious damage than would have been possible previously.
“As a result, we do not consider that there is necessarily a distinction in severity between espionage and the most serious unauthorized disclosures, in the same way that there was in 1989.
“Although there are differences in the mechanics of and motivations behind espionage and unauthorized disclosure offenses, there are cases where an unauthorized disclosure may be as or more serious, in terms of intent and/or damage.
“For example, documents made available online can now be accessed and utilized by a wide range of hostile actors simultaneously, whereas espionage will often only be to the benefit of a single state or actor.
“In severe cases, the unauthorized disclosure of the identities of agents working for the UK intelligence community, for example, could directly lead to imminent and serious threat to life.”
The Law Commission and the human rights organizations that helped draft the new proposals insist there should be a “public interest defense” in the amendment to protect journalists who receive leaked content.
However, the Home Office argues that such a provision would “undermine our efforts to prevent damaging unauthorized disclosures, which would not be in the public interest.”
A Home Office spokesman said:
“Freedom of press is an integral part of the UK’s democratic processes and the government is committed to protecting the rights and values that we hold so dear.
“It is wrong to claim the proposals will put journalists at risk of being treated like spies and they will, rightly, remain free to hold the government to account.
“We will introduce new legislation so security services and law enforcement agencies can tackle evolving state threats and protect sensitive data.
“However, this will be balanced to protect press freedom and the ability for whistleblowers to hold organizations to account when there are serious allegations of wrongdoing.”
July 20, 2021
Posted by aletho |
Civil Liberties, Corruption, Deception | UK |
4 Comments
Health research is based on trust. Health professionals and journal editors reading the results of a clinical trial assume that the trial happened and that the results were honestly reported. But about 20% of the time, said Ben Mol, professor of obstetrics and gynaecology at Monash Health, they would be wrong. As I’ve been concerned about research fraud for 40 years, I wasn’t that surprised as many would be by this figure, but it led me to think that the time may have come to stop assuming that research actually happened and is honestly reported, and assume that the research is fraudulent until there is some evidence to support it having happened and been honestly reported. The Cochrane Collaboration, which purveys “trusted information,” has now taken a step in that direction.
As he described in a webinar last week, Ian Roberts, professor of epidemiology at the London School of Hygiene & Tropical Medicine, began to have doubts about the honest reporting of trials after a colleague asked if he knew that his systematic review showing the mannitol halved death from head injury was based on trials that had never happened. He didn’t, but he set about investigating the trials and confirmed that they hadn’t ever happened. They all had a lead author who purported to come from an institution that didn’t exist and who killed himself a few years later. The trials were all published in prestigious neurosurgery journals and had multiple co-authors. None of the co-authors had contributed patients to the trials, and some didn’t know that they were co-authors until after the trials were published. When Roberts contacted one of the journals the editor responded that “I wouldn’t trust the data.” Why, Roberts wondered, did he publish the trial? None of the trials have been retracted.
Later Roberts, who headed one of the Cochrane groups, did a systematic review of colloids versus crystalloids only to discover again that many of the trials that were included in the review could not be trusted. He is now sceptical about all systematic reviews, particularly those that are mostly reviews of multiple small trials. He compared the original idea of systematic reviews as searching for diamonds, knowledge that was available if brought together in systematic reviews; now he thinks of systematic reviewing as searching through rubbish. He proposed that small, single centre trials should be discarded, not combined in systematic reviews.
Mol, like Roberts, has conducted systematic reviews only to realise that most of the trials included either were zombie trials that were fatally flawed or were untrustworthy. What, he asked, is the scale of the problem? Although retractions are increasing, only about 0.04% of biomedical studies have been retracted, suggesting the problem is small. But the anaesthetist John Carlisle analysed 526 trials submitted to Anaesthesia and found that 73 (14%) had false data, and 43 (8%) he categorised as zombie. When he was able to examine individual patient data in 153 studies, 67 (44%) had untrustworthy data and 40 (26%) were zombie trials. Many of the trials came from the same countries (Egypt, China, India, Iran, Japan, South Korea, and Turkey), and when John Ioannidis, a professor at Stanford University, examined individual patient data from trials submitted from those countries to Anaesthesia during a year he found that many were false: 100% (7/7) in Egypt; 75% (3/ 4) in Iran; 54% (7/13) in India; 46% (22/48) in China; 40% (2/5) in Turkey; 25% (5/20) in South Korea; and 18% (2/11) in Japan. Most of the trials were zombies. Ioannidis concluded that there are hundreds of thousands of zombie trials published from those countries alone.
Others have found similar results, and Mol’s best guess is that about 20% of trials are false. Very few of these papers are retracted.
We have long known that peer review is ineffective at detecting fraud, especially if the reviewers start, as most have until now, by assuming that the research is honestly reported. I remember being part of a panel in the 1990s investigating one of Britain’s most outrageous cases of fraud, when the statistical reviewer of the study told us that he had found multiple problems with the study and only hoped that it was better done than it was reported. We asked if he had ever considered that the study might be fraudulent, and he told us that he hadn’t.
We have now reached a point where those doing systematic reviews must start by assuming that a study is fraudulent until they can have some evidence to the contrary. Some supporting evidence comes from the trial having been registered and having ethics committee approval. Andrew Grey, an associate professor of medicine at the University of Auckland, and others have developed a checklist with around 40 items that can be used as a screening tool for fraud (you can view the checklist here). The REAPPRAISED checklist (Research governance, Ethics, Authorship, Plagiarism, Research conduct, Analyses and methods, Image manipulation, Statistics, Errors, Data manipulation and reporting) covers issues like “ethical oversight and funding, research productivity and investigator workload, validity of randomisation, plausibility of results and duplicate data reporting.” The checklist has been used to detect studies that have subsequently been retracted but hasn’t been through the full evaluation that you would expect for a clinical screening tool. (But I must congratulate the authors on a clever acronym: some say that dreaming up the acronym for a study is the most difficult part of the whole process.)
Roberts and others wrote about the problem of the many untrustworthy and zombie trials in The BMJ six years ago with the provocative title: “The knowledge system underpinning healthcare is not fit for purpose and must change.” They wanted the Cochrane Collaboration and anybody conducting systematic reviews to take very seriously the problem of fraud. It was perhaps coincidence, but a few weeks before the webinar the Cochrane Collaboration produced guidelines on reviewing studies where there has been a retraction, an expression of concern, or the reviewers are worried about the trustworthiness of the data.
Retractions are the easiest to deal with, but they are, as Mol said, only a tiny fraction of untrustworthy or zombie studies. An editorial in the Cochrane Library accompanying the new guidelines recognises that there is no agreement on what constitutes an untrustworthy study, screening tools are not reliable, and “Misclassification could also lead to reputational damage to authors, legal consequences, and ethical issues associated with participants having taken part in research, only for it to be discounted.” The Collaboration is being cautious but does stand to lose credibility—and income—if the world ceases to trust Cochrane Reviews because they are thought to be based on untrustworthy trials.
Research fraud is often viewed as a problem of “bad apples,” but Barbara K Redman, who spoke at the webinar insists that it is not a problem of bad apples but bad barrels if not, she said, of rotten forests or orchards. In her book Research Misconduct Policy in Biomedicine: Beyond the Bad-Apple Approach she argues that research misconduct is a systems problem—the system provides incentives to publish fraudulent research and does not have adequate regulatory processes. Researchers progress by publishing research, and because the publication system is built on trust and peer review is not designed to detect fraud it is easy to publish fraudulent research. The business model of journals and publishers depends on publishing, preferably lots of studies as cheaply as possible. They have little incentive to check for fraud and a positive disincentive to experience reputational damage—and possibly legal risk—from retracting studies. Funders, universities, and other research institutions similarly have incentives to fund and publish studies and disincentives to make a fuss about fraudulent research they may have funded or had undertaken in their institution—perhaps by one of their star researchers. Regulators often lack the legal standing and the resources to respond to what is clearly extensive fraud, recognising that proving a study to be fraudulent (as opposed to suspecting it of being fraudulent) is a skilled, complex, and time consuming process. Another problem is that research is increasingly international with participants from many institutions in many countries: who then takes on the unenviable task of investigating fraud? Science really needs global governance.
Everybody gains from the publication game, concluded Roberts, apart from the patients who suffer from being given treatments based on fraudulent data.
Stephen Lock, my predecessor as editor of The BMJ, became worried about research fraud in the 1980s, but people thought his concerns eccentric. Research authorities insisted that fraud was rare, didn’t matter because science was self-correcting, and that no patients had suffered because of scientific fraud. All those reasons for not taking research fraud seriously have proved to be false, and, 40 years on from Lock’s concerns, we are realising that the problem is huge, the system encourages fraud, and we have no adequate way to respond. It may be time to move from assuming that research has been honestly conducted and reported to assuming it to be untrustworthy until there is some evidence to the contrary.
Richard Smith was the editor of The BMJ until 2004.
Competing interest: RS was a cofounder of the Committee on Medical Ethics (COPE), for many years the chair of the Cochrane Library Oversight Committee, and a member of the board of the UK Research Integrity Office.
July 20, 2021
Posted by aletho |
Corruption, Deception, Science and Pseudo-Science, Timeless or most popular |
Leave a comment

One commonly used trick in drug trials is to exclude any group that might make the drug look worse, such as those that are more likely to experience side effects. A good recent example of this is the covid vaccine trials, which largely excluded people with auto-immune diseases (more likely to develop an auto-immune disease after vaccination), people with allergies (more likely to have an allergic reaction to the vaccine), and, of course, the elderly (less likely to develop immunity after getting the vaccine, and more likely to become seriously sick from it).
These three groups are all frequently excluded from trials, and the exclusion is particularly galling when it comes to the elderly, because they are a big segment of the population, and they are also usually the most likely to end up actually using the drugs being tested.
When drug companies have gotten a drug approved, and move on to market the drug, they will studiously avoid mentioning the fact that large segments of the population were excluded from the trials. When drug reps show their flashy powerpoints to gatherings of doctors, say for a new drug to lower blood pressure, they will always present impressive looking graphs of benefit, and they will of course point out how safe their drug was shown to be in the trials. Not once will they mention that the groups of patients the doctors will primarily be prescribing the drug to weren’t even included in the trials.
The doctors will then happily go off and prescribe the drug to multi-morbid 90 year olds, which might explain why prescription drugs are now the third leading cause of death in the western world.
The manipulation of who is included in trials is probably one of the main reasons why findings of side effects always end up being much higher in reality than in clinical trials. It might explain, for example, why muscle pain is a massively common side effect of statins in the real world, while being vanishingly rare in the statin trials (as Dr. Malcolm Kendrick has written about in detail).
A study recently published in the Lancet Healthy Longevity sought to estimate the extent to which drug trials underestimate side effects. It was funded by the UK Medical Research Council and the Wellcome Trust. The study chose as its particular focus people being treated for high blood pressure with a certain class of blood pressure lowering drugs known as RAAS blockers (which includes all drugs with names ending in -pril and all drugs with names ending in -sartan). The advantage with looking at this particular class of drugs is that there are a ton of trials. Every major pharmaceutical company has its own RAAS-blocker. It should therefore be possible to draw relatively broad conclusions about the results – whatever they show, they apply to the entire pharmaceutical industry, not just to a few specific companies. It’s also reasonable to think that the results apply to other classes of drugs too – there’s no reason to think trials of RAAS-blockers have been done differently than trials of other drug classes.
What the study sought to do more specifically was compare the rate of serious adverse events in clinical trials of RAAS-blockers with the rate observed in the real world. A serious adverse event is any event that is potentially life threatening or that results in death, hospitalization or lasting disability. If a trial has been designed in such a way that it is representative of reality, then the rate of serious adverse events in the trial should largely mirror that seen in the real world.
110 trials of RAAS-blockers were identified by the researchers. Of these, 11 were specifically designed to look at older people (i.e. didn’t recruit anyone under the age of 60). The data on serious adverse events from these 110 trials was extracted and compared to real world data on deaths and hospitalizations taken from a UK government funded database of 55,000 people living in Wales, who were being treated with RAAS-blockers. Deaths and hospitalizations are not exactly the same thing as serious adverse events (which as mentioned above also include “life threatening events”, and could for example include someone who is treated in an emergency department after a fall but not admitted to the hospital), but they’re close enough to allow a reasonable comparison.
So, what were the results?
Let’s begin with comparing the trials of older people with the “standard” trials. The relative rate of serious adverse events in the trials of older people was 76% higher than the rate in the standard trials. This shows the importance of including elderly people in drug trials – they are much more likely to experience adverse events of all kinds (including those actually caused by the drug being tested), and excluding them will therefore likely underestimate side effects.
Considering that many of the drugs in common use show marginal benefits at best (statins have, for example, only been shown to prolong life by a few days on average), this is important information. Why? Because a drug that is beneficial, on balance, to a fifty year old, who has a fully functioning kidney and liver, and is therefore unlikely to suffer side effects, could easily be harmful, on balance, to an 80 year old.
That’s why drug studies done on younger people should not be used to guide treatment of older people. No shock there. Everyone already knows that we shouldn’t be extrapolating results from one group to another (even though it happens all the time, as we’ve seen most recently with the covid vaccine trials).
Next we come to the more important, and perhaps more shocking finding.
The real world patients were between 300% and 400% more likely to experience a serious event than the participants in the trials! That is in spite of the fact that the trials, as mentioned above, were using a broader definition of what constituted a serious event. If the trials were representative of reality, then they should have a higher rate of events than is seen in the real world data. Instead they have a rate that is several times lower!
Interestingly, the trials of older people were just as far from the real world results as the trials of younger people. Clearly, doing trials on the elderly is not enough on its own to produce trials that are representative of reality. What’s happening here exactly?
There are three possible explanations, as far as I can see. The first explanation is that the trials are representative of reality, but that the Welsh die and are hospitalized at a rate that is several times higher than people in the countries where the studies were conducted. Many of the trials were conducted in the US, not in Wales. But Wales has a higher life expectancy than the United States, so that seems unlikely. I think we can discount that explanation.
The second explanation is that the trials are unrepresentative in so many different ways that just correcting the age issue doesn’t make a noticeable difference. That’s probably part of the explanation. The average age even in the trials of “older people” was 73, which isn’t very old from my perspective. And those 73 year olds included in the trials were probably at the healthier end of the spectrum.
The third, more sinister explanation, is that the pharmaceutical companies are hiding serious adverse events… But wait a minute, the trials are randomized and blinded, so the people running the drug trials have no way of knowing if someone experiencing a possible side effect is in the treatment group or the placebo group, right?
Yes, that’s right, so the easiest solution, if you want to avoid finding nasty side effects, is to not report them, regardless of which treatment group the participant is in. That will cut down on total adverse events in both groups, which will make any difference between the groups that does exist smaller in absolute terms, and also less likely to reach the level of statistical significance. Voila – the treatment group and the placebo group end up having similar rates of side effects, and the drug company can conclude that the drug is completely safe.
Is that what’s happened here? Are the pharmaceutical companies hiding adverse events? Well, it’s very strange that the real world data shows a rate of serious adverse events that is several times higher than is found in the trials. It’s hard to see how that massive difference could be explained in any other way.
So, how big a problem is this?
Big. Very big. It should shake the very foundations of evidence based medicine. If the drug trials and the real world data show such wildly different rates of adverse events, then it really begs the question how much we can trust the trials at all. It would be perfectly reasonable in this situation to say that all “evidence” produced by pharmaceutical companies is so suspect that it should be dismissed out of hand, and that only independently funded trials should be used as a basis for medical treatment decisions.
The problem with that is that it would mean saying goodbye to most of the trials that form the basis of modern medical treatment, and there is not much to replace them with. This issue could be solved over the longer term through large tax payer funded investments in new independent trials. But there’s no quick fix.
The problem is most acute when it comes to the many drugs in common use that only show marginal benefits, such as statins. If the rate of side effects is actually 300% to 400% higher than seen in the trials, then the harms of these drugs could easily outweigh the benefits. In other words, the cost-benefit calculation could shift entirely for many of the most commonly used drugs.
Ok, let’s wrap this up. What can we conclude?
Drug trials do no accurately represent rates of adverse events. It is likely that the true rate of side effects is often many times higher than that seen in drug trials.
July 19, 2021
Posted by aletho |
Corruption, Deception, Science and Pseudo-Science, Timeless or most popular |
1 Comment

WITH an estimated fortune of $128.9billion, Bill Gates is the fourth richest man in the world, after Amazon’s Jeff Bezos, Bernard Arnault and Elon Musk, according to Forbes.
He’s stepped back from the day-to-day running of Microsoft, the company he founded in 1975, and focuses on his so-called philanthropy through the Bill & Melinda Gates Foundation (GF), and is best known for his worldwide vaccination and anti-malaria programmes.
Less widely known is that he has spent hundreds of millions bankrolling news outlets, in the process turning the GF into one of journalism’s main gatekeepers. According to Tim Schwab of Columbia Journalism Review, by last June more than $250million had gone to news operations including the BBC, NBC, Al Jazeera, ProPublica, National Journal, the Guardian, the Financial Times, Univision, Medium, the Atlantic, the Texas Tribune, Gannett, Washington Monthly, Le Monde, and the Center for Investigative Reporting; and to charitable organisations affiliated with news outlets, like the BBC’s Media Action and the New York Times’s Neediest Cases Fund.
As I reported in Part One of this investigation, most of this funding comes under the fine sounding GF heading of Global Policy and Advocacy, of which the BBC is a major beneficiary. Little wonder that there is little that is dispassionate about its reporting on Covid-19 vaccination or climate change.
It’s not just the BBC that the GF manipulates through these means. Between 2016 and 2020, the Financial Times received $2.3million from the GF, including $1.3million to fund ‘global health awareness’. The Guardian is another recipient of Mr Gates’s largesse. Like the BBC, it sports a ‘Global Development’ site, the common root being GF funding. Its claimed editorial independence is contradicted by its stated sole campaigning purpose to provide special focus on the Millennium Development Goals, eight targets set in 2000 by the United Nations Millennium Declaration. The Guardian has bought into this to the extent that it operates mainly as a deferential PR channel for both the UN and the GF.
The collaboration with the GF to ‘help focus the world’s attention on global development’ goes back 11 years. This is a sophisticated propaganda exercise to convince the public of the beneficial nature of Gates’s investments in a multitude of global development projects including vaccines and solutions for climate change. It helps ensure that any alternative narrative or critique is unlikely to see the light of day in any of the outlets to which he extends his munificence.
Since August 2011, the GF has given the Guardian $12.2million towards this, the latest grant being almost $2million last September. The Guardian has not only busily promoted the Millennium Development Goals, but also its spawn, the UN 2030 Agenda for Sustainable Development, yet another dishonest scheme to take guilt money from Western taxpayers and give it to the world’s despots and dictators, all in the name of climate change.
Yet, as I have previously set out: ‘Very little information is available on exactly how the money is invested and who benefits from it. No information is offered to indicate if it has been cost-effective and beneficial to the economies and welfare of the 193 countries signed up to it.’
The British public have been drip-fed this propaganda for years through various GF-funded MSM mouthpieces such as the BBC. Yet it’s the economically fragile West which pays for the 2030 Agenda and its climate change ‘remedies’, draining it of even more of its resources while authoritarian regimes like China benefit financially and increase their dominance over the UN. The MSM barely protests.
The worry is that the GF has not only captured the Left-wing media in Britain: it has also made inroads into the so-called Centre and Right. The Telegraph accepted $3.4million from the GF in November 2017 to ‘raise awareness’ of global health issues. The London Evening Standard was awarded money in the same year too, receiving $20,000 to spread the GF propaganda on the ‘global health crisis’.
The growing financial dependence of the MSM on a combination of Government advertising and GF largesse has already put its impartiality in jeopardy. This is threatened further by the GF’s funding of a global network of young ‘journalists’. This project, called the International Centre of Journalists, has been given $20.4million to promote ‘public awareness’ around global health. Based in the US, the organisation finances activists to promote ‘better governments’ and make ‘communities safer and healthier’, amongst other woke ideals. Their 2020 annual review predictably emphasises the need to highlight racial injustice and climate change, and combat ‘disinformation’ about Covid-19.
As Robert Kennedy Junior says, Gates’s press bribes have paid off. ‘During the pandemic, bought and brain-dead news outlets have treated Bill Gates as a public health expert despite his lack of medical training or regulatory experience.’
Gates also funds an army of independent fact checkers including the Poynter Institute and Gannett which, Kennedy points out, use their platforms to silence detractors and to debunk as ‘false conspiracy theories’ and ‘misinformation’ charges that Gates has championed and invested in sinister endeavours like biometric chips, vaccine passports and satellite systems.
Yet all the evidence is available at a click of a mouse button. Last March, Gates began his vaccine passport campaign. The GF-funded Guardian and the BBC have unquestionably cheered on this digital slavery. In 2018, Gates gave a satellite start-up $1billion to build a system which broadcasts real-time videos globally. What better way to ensure that the little people are behaving themselves than by funding a satellite system to monitor us all? Despite the vehement denials of the GF funded ‘fact checkers’, Gates has built his Covid-19 vaccine factories, and seemingly now seeks a return on his investments.
Many lament the decline of journalistic standards in our New Dark Age. Of those responsible for turning a once-brilliant British media into an uncritical disseminator of propaganda, the GF must be placed centre stage. Now the MSM, like the Government, are often nothing more than useful idiots for the GF and its destructive policies, mindlessly chanting the GF narrative on development, climate change and Covid-19; and whose ‘solutions’ to these are destroying the free and prosperous West.
Don’t expect our MSM journalists to protest: they have long since been bought, paid for and brainwashed.
July 16, 2021
Posted by aletho |
Corruption, Mainstream Media, Warmongering, Science and Pseudo-Science | UK |
Leave a comment
The notorious case of former top Mexican official wanted in connection with the torture, abduction and murder of 43 students, and for embezzling $50 million of state funds, has become mired in a diplomatic tussle between Israel and Mexico over the occupation state’s treatment of Palestinians.
Tomás Zerón de Lucio, the former director of Mexico’s equivalent of the FBI, fled to Israel following the opening of an investigation into his role in the 2014 Iguala mass kidnapping, which continues to cause a storm in Mexico to this day. Zeron headed the criminal investigation, but his report was discredited after it was discovered that crucial testimony was obtained under torture, evidence was mishandled and promising leads ignored.
Zeron has dismissed the charges and has been seeking political asylum in Israel, where he has lived for nearly two years. Mexican officials say that Zeron has connections to powerful Israeli companies that helped him flee Mexico.
Allegations against the former official also include the embezzlement of $50 million worth of state funds. While in office, Zeron is said to have authorised the purchase of tens of millions of dollars in surveillance systems from private Israeli intelligence firms including the notorious Pegasus software developed by Israel’s NSO Group. The software has been used to target journalists, lawyers and activists in several countries around the globe. It’s claimed that in some cases the intelligence gear purchased by Zeron were never delivered.
Mexico has demanded the extradition of Zeron. Israel however has not acted on either the extradition request or the asylum claims and is said to be looking for ways to squeeze diplomatic concessions out of the highly sensitive case.
Senior Israeli officials were cited in the New York Times saying that Zeron’s extradition case was being slow-walked as “tit-for-tat diplomacy” against Mexico, which has supported United Nations inquiries into allegations of Israeli war crimes against Palestinians. “Why would we help Mexico?” the official said, speaking on condition of anonymity to offer a candid view of a diplomatic dispute.
The senior Israeli official said that the current Mexican government has repeatedly supported resolutions criticising Israel at the UN Human Rights Council in Geneva, including decisions to investigate Israel’s killing of Palestinian protesters in Gaza in 2018 and the killing of civilians in the besieged enclave during the occupation state’s latest onslaught.
July 16, 2021
Posted by aletho |
Civil Liberties, Corruption | Human rights, Israel, Mexico, Palestine |
1 Comment
Yesterday we reported evidence given to the German-led international Corona Investigative Committee on Friday July 9 by Dr David Martin, who runs a US company monitoring innovations relevant to financial interests. He said a review of more than 4,000 patents issued around the SARS (Severe Acute Respiratory Syndrome) coronavirus had led to the dramatic conclusion: ‘We made SARS’. Today we continue an account of his evidence, of which the live-streamed video is here.
THE United States has a federal law known as the RICO Act. It sounds friendly, but is aimed at something deadly: Racketeer Influenced and Corrupt Organisations. It was introduced due to the complexity of bringing successful charges against organised crime gangs.
Dr David Martin told the Corona Investigative Committee that in April 2003, a US drug company applied for a patent on anti-viral agents, treatment, and control of infections by coronavirus, just three days after the Centres for Disease Control sought to patent the SARS coronavirus itself – in a supposedly secret application. The first SARS outbreak had occurred in February that year in China.
His description led the inquiry committee chairman, German lawyer Reiner Fuellmich, who specialises in exposing corporate swindles, to comment: ‘This could well blow up into a RICO case ultimately.’
Martin replied: ‘Not could blow up – it is a RICO case. And the RICO pattern which was established in April 2003 for the first coronavirus was played out to exactly the same schedule when we see SARS-COV-2 show up.’
He claimed that Moderna (originally ModeRNA) were given the genetic sequence for the spike protein that forms the basis of their Covid vaccine by phone from the vaccine research centre at the National Institute of Allergy and Infectious Diseases even before the novel subclade of the virus had been defined. ‘How do you treat a thing before you actually have the thing?’ he asked.
Moderna (originally ModeRNA Therapeutics) is a Massachusetts-based company founded in 2010 by a team of investors to develop RNA (ribonucleic acid) technology, thought to hold huge promise in harnessing the power of RNA code to make new medicines inside our bodies.
Another important date, Martin said, is June 5, 2008. This was around the time when the Defence Advanced Research Programme (DARPA) in the US took an interest in coronavirus as a biological weapon. It was also the date when a drug company, now part of the Paris-based pharma giant Sanofi, filed a series of patents targeting genes that 12 years later are said to be the novel features of SARS-COV-2 that make it a health hazard for humans.
From 2008 onwards, patent filings from numerous organisations identified ‘every attribute’ of the virus, as it eventually came to be described. The reference paper routinely used to identify it, published in March 2020, claimed to show that the novel features had come about in nature, and that the virus ‘originated from multiple naturally-occurring recombinant events among those viruses present in bats and other wildlife species’.
Martin said: ‘Unfortunately, if you actually take what they report to be novel, you find 73 patents, issued between 2008 and 2019, which have the elements which are allegedly novel in SARS-COV-2. So – there was no outbreak of SARS, because we had engineered all of the elements of that.’
The supposedly new virus had been said since 2016 to be poised for human emergence. But ‘it was not only poised for human emergence, it was patented for commercial exploitation – 73 times,’ Martin said. ‘Any assertion that this pathogen is somehow unique or novel falls apart on the actual gene sequences, which are published in the patent record.’
Researchers at the University of North Carolina at Chapel Hill (who collaborated with the laboratory in Wuhan, China, in the coronavirus ‘gain of function’ work) along with the National Institute of Allergy and Infectious Diseases and Moderna, began the sequencing of a spike protein vaccine in November 2019, a month before the Wuhan outbreak happened.
Martin also challenged the idea that injecting people with the RNA sequence for the spike protein is a true vaccine. The theory behind it is that by teaching the immune system to recognise the protein, which in itself has toxic effects, the body will be better equipped to deal with the toxin when exposed to the virus.
‘The illusion that we continue unfortunately to see very well-meaning people get trapped in, is conversations about whether we are having a vaccine for a virus. The fact is, we’re not. We are injecting a spike protein RNA sequence, which is a computer simulation of a sequence which has been known and patented for years. It’s not derived from nature.
‘The ludicrous nature of the story that this is somehow prophylactic or preventative flies in the face of 100 per cent of the evidence, because the evidence makes it abundantly clear that there has been no effort by any pharmaceutical company to combat the virus. This is about getting people injected with the known-to-be harmful spike protein.’
The reason for doing that, he argues, is to get people ‘addicted’ to a pan-coronavirus vaccine. There had been a decade-long, pan-influenza vaccine mandate, ‘desperately, desperately, desperately promoted by governments around the world. They failed. And they decided if influenza doesn’t deliver, on the public promise of getting everybody to get an injection, let’s change the pathogen.
‘You need to create the illusion of a demand, and there is nothing right now that does a better job of creating the illusion of demand than the urgency of an event you have manufactured.
‘Here’s the sad and sober irony: I raised these issues in 2002, after the anthrax scare, and the tragedy is we are now sitting in a world where we have hundreds of millions of people who are being injected with a pathogen-stimulating computer sequence which is being sold under what the Patent Office, the medical profession, and the FDA (Food and Drug Administration) in its own clinical standards would not suggest is a vaccine. But by using the term, we are now subjecting hundreds of millions of people to what was known by 2005 to be a biological weapon.’
The video of Martin’s live-streamed evidence is already receiving tens of thousands of views. At the very least, the data he presents surely should put to rest the idea of the virus as a product of nature that just happened to develop the capacity to jump from animals to humans.
This in itself has enormous implications. For one thing, why should we believe the claims by the Coalition for Epidemic Preparedness (CEPI), launched in 2017 with a huge cash infusion from the Gates Foundation, that a proposed 3.5billion-dollar quest for a universal coronavirus vaccine to ‘contain SARS-COV-2 and its variants’ is either a desirable or an achievable goal?
Urging support for the plan, co-founder Bill Gates said ‘CEPI has helped the global science community do something incredible: develop Covid-19 vaccines in less than a year.’ That claim sounds more than hollow in the light of the 20-year patent trail revealed by Martin.
What’s more, Martin spelled out a case that even the alleged SARS ‘variants’ of the coronavirus are artificial, representing the identification of different gene fragments rather than genuine variations.
‘It’s just an alteration in when you start and stop what you call the reading frame,’ he said. ‘If what we are looking for is something we have decided is worth looking for, then we’ll find it … where I choose to start or stop, I can say I found it. Or I didn’t find it! I didn’t find the match that I projected on to the data, because I chose to look at the data in a way that I could not find the match.’
With government advisers seemingly pulling ‘new variants’ out of the bag whenever they feel the grip of terror is lessening, this is another area calling for a sober reassessment of what is really going on.
July 15, 2021
Posted by aletho |
Corruption, Science and Pseudo-Science, Timeless or most popular | Covid-19, COVID-19 Vaccine |
Leave a comment
A 20-YEAR trail of patent applications concerning the virus responsible for Covid-19 proves it is neither new nor the result of a jump from animals to humans, an inquiry has been told.
Instead, the patents show that a natural virus, harmless to humans, was subjected to numerous laboratory modifications which ‘weaponised’ it, such that it could become the basis of a marketing campaign for tests and vaccines which are of questionable value to the public health, but which have proved to be a financial bonanza for drug companies.
A dossier of evidence supporting these claims has been presented to the international Corona Investigative Committee headed by Reiner Fuellmich, a senior German lawyer specialising in exposing corporate swindles. The committee has been taking testimony from scientists and other experts since July last year.
The dossier was submitted last week by Dr David Martin, who heads M-CAM International, a US company which monitors innovations relevant to financial interests.
First made public more than a year ago, Martin’s allegations were widely dismissed as ‘conspiracy’ by so-called fact-checkers, who at the time were promoting the view fostered by the scientific establishment that the virus had a natural origin.
That view has become seen as in itself based on a conspiracy to mislead involving British scientist Dr Peter Daszak, head of the EcoHealth Alliance, which has received tens of millions of US dollars for investigating coronaviruses, but who was appointed by the Lancet medical journal to head an inquiry into the virus’s origins.
Last month Daszak ‘recused himself’ without explanation from the inquiry. He played a leading role in a similar investigation by the World Health Organisation, widely dismissed as a whitewash when published on March 30.
On Friday last week Martin gave a two-hour, live-streamed interview to Fuellmich and his team in which he spelled out the patent data that led to his explosive conclusions; you can watch it here.)
He said that ‘somebody knew something in 2015 and 2016 which gave rise to my favourite quote of this entire pandemic’. This was a statement made by Peter Daszak in 2015, and reported in the National Academies Press on February 12, 2016, in which he declared: ‘We need to increase public understanding of the need for medical counter-measures such as a pan-coronavirus vaccine. A key driver is the media, and the economics will follow the hype. We need to use that hype to our advantage, to get to the real issues. Investors will respond if they see profit at the end of the process.’
Of his own company, Martin said: ‘We have since 1998 been the world’s largest underwriter of intangible assets used in finance in 168 countries. Our underwriting systems include the entire corpus of all patents, patent applications, federal grants, procurement records, e-government records, etc. We have the ability to track not only what is happening, and who is involved in what’s happening, but we monitor a series of thematic interests for a variety of organisations and individuals as well as for our own commercial use.
‘We have reviewed over 4,000 patents issued around SARS-coronavirus and done a very comprehensive review of the financing of all the manipulation of coronavirus which gave rise to SARS (Severe Acute Respiratory Syndrome).
‘We took the actual genetic sequences that were reportedly novel, and reviewed those against the patent records available as of the spring of 2020. What we found, as you’ll see in this report, are over 120 patented pieces of evidence to suggest that the declaration of a novel coronavirus was entirely a fallacy. There was no novel coronavirus. There are countless, very subtle modifications of coronavirus sequences that have been uploaded. But there was no single identifiable novel coronavirus at all.
‘As a matter of fact, we found patent records of sequences attributed to novelty going to patents sought as early as 1999. So not only was this not a novel anything, it’s actually not been novel for over two decades.’
Martin took the inquiry team on what he called a ‘short journey through the patent landscape, to make sure people understand what happened’.
Until 1999, he said, patenting activity around coronavirus applied only within veterinary science. As early as January 2000, the Pfizer drug company filed for a patent on a genetic sequence giving rise to a coronavirus spike protein, ‘the exact same thing we have allegedly rushed into invention’, to be used in a vaccine against a canine disease.
So, based on patent filings more than two decades old, neither the coronavirus concept of a vaccine, nor the principle of the coronavirus itself as a pathogen of interest with regard to the spike protein’s behaviour, were ‘anything novel at all’.
Even more problematic, the patent record showed that in 1999 Anthony Fauci, head of the US National Institute of Allergy and Infectious Disease (NIAID), found the ‘malleability’ of the coronavirus made it a potential candidate for vaccines against HIV (the purported cause of AIDS, for which US taxpayers have contributed more than $300billion in research and treatment over the past 35 years).
‘Anthony Fauci funded research at the University of North Carolina, Chapel Hill, specifically to create – and you cannot help but lament what I am about to read, because this comes directly from a patent application filed on April 19, 2002 – “an infectious replication defective coronavirus”.’
This virus was specifically targeted to invade human lung epithelia, the protective cells lining the lungs, Martin said.
‘In other words, we made SARS. Before there was ever any alleged outbreak in Asia, which as you know followed that by several months.
‘That patent, issued as US patent 7279327, clearly lays out in very specific gene sequencing the fact that we know that the . . . ACE-2 binding domain [a protein on the surface of many cell types, through which both SARS-CoV-2 and the original SARS coronavirus enter host cells], the S1 spike protein, and other elements of what we have come to know as this scourge pathogen, was not only engineered but could be synthetically modified in the laboratory, using nothing more than gene sequencing technologies taking computer code, and turning it into a pathogen.
‘And the technology was funded exclusively in the early days as a means by which we could harness coronavirus as a vector to distribute HIV vaccine.’
Martin went on: ‘It gets worse.’ His organisation was asked to monitor biological and chemical weapons treaty violations, and was part of an investigation into events in October 2001, in which letters containing anthrax spores were sent to several news media offices and two senators.
‘Throughout the fall of 2001 we began monitoring an enormous number of bacterial and viral pathogens that were being patented through the National Institutes of Health, NIAID, USAMRIID [the US Army Medical Research Institute of Infectious Diseases], and a number of other agencies internationally that collaborated with them.
‘Our concern was that coronavirus was being seen not only as a potential manipulable agent for potential use as a vaccine vector, but it was also very clearly being considered as a biological weapon candidate.
‘Our first public reporting on this took place prior to the SARS outbreak in the latter part of 2001. So you can imagine how disappointed I am to be sitting here 20 years later, having 20 years earlier pointed that there was a problem looming on the horizon with respect to coronavirus.’
That first SARS event gave rise to a ‘very problematic’ April 2003 patent filing by the US Centers for Disease Control and Prevention (CDC). It was for the entire SARS gene sequence, and for a series of derivative patents covering means of detection, including the PCR test [widely used today purportedly to diagnose cases of SARS-CoV-2 infection].
‘The reason why that is a problem is that if you both own the patent on the gene itself, and on its detection, you have a cunning advantage to being able to control 100 per cent of the provenance of not only the virus itself, but also its detection. Meaning, you have the entire scientific and message control.’
The CDC’s public relations team sought to justify the application on the grounds that it would enable everyone to be free to research coronavirus.
That was a lie, Martin said. The US Patent Office twice rejected the application for the entire SARS sequence, on the grounds that it was already recorded in the public domain, but the CDC started a process to override this rejection. After repeated applications, and paying an appeal fine, they got the patent approved in 2007. They also paid an additional fee to keep the application private. ‘So every public statement the CDC has made that said this was in the public interest is falsifiable by their own, paid bribe to the Patent Office.’
Furthermore, three days after the CDC’s April 2003 attempt to patent the SARS sequence, Sequoia Pharmaceuticals, a private venture-capital funded company founded in 2002, filed a patent application on antiviral agents, treatment and control of infections by coronavirus. This was approved, and published, before the CDC patent was allowed.
‘So the degree to which the information could have been known by any means other than insider information between those parties is zero. It is not physically possible for you to patent a thing that treats a thing that had not been published, because CDC had paid to keep it secret.
‘This is the definition of criminal conspiracy, racketeering and collusion. This is not theory. This is evidence.’
July 14, 2021
Posted by aletho |
Corruption, Deception, Timeless or most popular | Covid-19 |
1 Comment