This post from our Economics Correspondent is closely linked to Remind Your Sister to Get Vaccinated and also Treatment Great, Patient Died.
Portmeirion Village in North Wales provided the backdrop for a 1960s Cult Classic series, The Prisoner, starring Patrick McGoohan. McGoohan was ‘Number Six’. At its core was the Prisoner’s unwillingness to be a number.
We are all on our way to being imprisoned by our numbers if the drug companies, rebranded as “Life Sciences”, get their way. In Europe Big Pharma is straining to extract Big Data from of all of us. Their vision of the future is having unfettered access to all our health-data.
There will be no escape for the unvaccinated; no rest for those with high cholesterol or at risk of sarcopenia, the muscle wasting we all get as we age. Where our doctors once knew us as people, we will be known instead by a number, a risk score, and other data. The Health Police will call us in for our flu jab and to tell us we will be deregistered from the clinic if we don’t get our cholesterol level down. We may lose health insurance on the basis of untreated ‘pre-diabetes’. Those of us who comply will rattle – not from our chains but from our pills. Polypharmacy R Us.
The Quest for Big Data
Computerisation of medical data has been slowly developing over the past 50 years. There are good sides to this – better disease and prescription drug coding. Overcoming the problem of doctors’ illegible handwriting.
Sharing computerised essential health data makes some sense within a single country like the UK or across a large private health service company like Kaiser Permanente.
You could argue it might help with cross-border sharing of data – so that for instance doctors treating a Finn becoming ill in Greece can access their health record. But these are uncommon events, which these days are easily managed by phone or email.
But Europe is where the problems come into focus. Some of Europe’s problems are explained in this video by a gloomy Ioana-Maria Gligor, Digital Health Unit Head at the European Commission.
Brexit was caused by Brits resistance to Free Movement of Labor, which is a central tenet of the EU. But the EU in turn has led the world in clamping down on Free Movement of Data. It put in place the General Data Protection Regulation (GDPR). Companies from Google through to the Life Science outfits hate GDPR.
Industry will have the opportunity to make use of the Health Data Access Bodies, after they have been granted a permit for access to data. Only the data necessary for that specific research would be put at their disposal, without revealing individual’s identity, and it can only be accessible in the secure processing environment for the duration of their project.
In the context of healthcare, the European Health Data Space (EHDS) only supports the access of health professionals to the data of their patients. The view was that Industry will not have access to such data. Paradise.
Trouble in the Garden
This has set up a clash between the EU and the Life Science guys. Watching the LiScis maneuver is like watching the Snake tempt Adam (Given that Lilith was written out of the original story – who knows what happened).
On the Seventh Day God, Satan or Someone created TEHDAS – Towards the European Health Data Space.
TEHDAS is advised by EFPIA (European Federation of Pharmaceutical Industries and Associations).
“TEHDAS helps EU member states and the European Commission to develop and promote concepts for the secondary use of health data to benefit public health and health research and innovation in Europe. Our goal is that in the future European citizens, communities and companies will benefit from secure and seamless access to health data regardless of where it is stored.”
Then there is The European Institute for Innovation through Health Data, i~HD was created in 2016 as the sustainable result of the IMI (Innovative Medicines Initiatives) -EFPIA sponsored project Electronic Health Records for Clinical Research (EHR4CR) and a number of other European R&D projects supported by the European Commission. Its members include industry giants like A-Z, Novartis and ICON – who ran what everyone else calls the Pfizer vacccine trial. They already issue their own certificates of GDPR compliance.
The IMI/EFPIA Health Outcomes Observatory project (H2O)
“brings together the public and private sectors to create an unprecedented, standardised data governance and infrastructure system across Europe to incorporate patients’ experiences and preferences in decisions affecting their individual health care and those of the entire patient community”.
This H2O video explains that we need Data as much as we need Water and how patient organizations, universities and pharmaceutical companies are joining together to design the healthcare of the future.
World Economic Forum
Bert meets Bill at the most recent World Economic Forum (WEF) in Davos. Two weeks before this photograph was taken the BFG had tested positive for COVID. I wonder how the conversation with Albert went. Albert has since had two doses of COVID
The WEF is a bete noire for many. It has intimate links to the World Health Organization (WHO) – the body whose guidelines tell investigators not to attribute an adverse event to a vaccine in a clinical trial. Looking at WEF and WHO pronouncements, many worried about a World Government taking shape. Two years ago WEF produced ‘Sharing Sensitive Health Data in a Federated Data Consortium Model’, which claims:
In the current era of the Fourth Industrial Revolution, data is our most valuable resource – more valuable than oil.
The ICON (Pfizer) trial data were written up and published online in the New England Journal of Misinformation within four weeks of the trial ending. As things stand, Albert in his book MoonShot regards this as too slow. With A.I. we will soon have authoritative articles published online the day after the trial ends – without any clinical or regulatory oversight.
Trust
This is where Pharma has a spot of bother. A large majority of citizens are content for their anonymised health data to be used in research by universities for the good of mankind. However, many draw the line at their data being used by commercial companies. According to a survey 93% of patients do not trust advice from pharmaceutical companies about their medication.
Arthur M Sackler – the guy who bought Purdue Pharma and gave it to his slightly slower brothers – is a great candidate for the Svengali of twentieth century health services. AMS created IMS in the 1950s. IMS later called IMS Health pioneered the quest for Big Data. The mission was to get the data on what drugs every doctor was using and not using into company hands. Once it took off, Sales Reps visiting doctors armed with this information knew more about what the doctor was doing than s/he knew herself.
IMS was rebranded to IQVIA some years ago when it also got into the clinical trial business getting the data According to IQVIA, secondary data can help Pharma:
- Understand the current standard of care
- Identify unmet medical needs or existing treatment obstacles
- Trace disease progression, diagnosis, and treatment trends
- Assess the safety and efficacy of existing treatment interventions
- Support protocol design and feasibility to optimize studies from primary data
- Identify the best sites and most appropriate patients for studies from primary data
- Conduct safety surveillance and signal detection
- Demonstrate cost of illness and Healthcare Resource Utilization (HCRU)
- Collect evidence for negotiating optimal pricing, reimbursement, and coverage
- Forecast and track brand performance
- Support targeted campaigns, inform messaging, and hone market strategy
IQVIA is the largest global healthcare data vendor in the world.
Data Saves Lives
Data Saves Lives is:
“a multi-stakeholder initiative with the aim of raising wider patient and public awareness about the importance of health data, improving understanding of how it is used and establishing a trusted environment for multi-stakeholder dialogue about responsible use and good practices across Europe”.
It is led by the industry dominated European Patients’ Forum (EPF) and the European Institute for Innovation through Health Data (i~HD)
DSL is tied up with Nicola Bedlington’s EFPIA Patient Think Tank. Nicola is also a member of the Patient Advisory Council of the clinical research Drug Information Association DIA,
“the only independent organization that brings together regulatory authorities from across the globe in an international Council of Regulators.”
Data Saves Lives helpfully produces a toolkit to help patient groups spread the word about data sharing. In other words, Pharma-backed DSL helps patient groups help Pharma – as outlined in Remind your Sister to Get Vaccinated.
Although not in Europe, Britain’s National Health Service has its own version of Data Saves Lives – called Data Saves Lives. Everyone in Britain knows that their data is going online – making it possible to access your records through an App.
As outlined in comments on recent posts, many doctors are resisting this – but not because of their concerns about our privacy. It’s far more a case of them not wanting us to see what they have written about us. This of course makes it irresistible for us to insist on transparency – and hand over our data to people even less interested in oiur welfare than the local family doctor.
Ben Goldacre appears heavily involved in mobilizing health data in the UK for broader noble purposes – just as he was with AllTrials – a pharmaceutical company initiative aimed at blocking access to data from company studies while giving the appearance of supporting responsible access.
See Fucked, Follow the Rhetoric , First Admit no Harm, Follow the Lawsuit and Follow the Patient.
There is also the Ethical Medicines Industry Group – EMIG – which has echoes of Sense about Science and AllTrials. EMIG is keen to contribute to British efforts to build back better after COVID – by ensuring we are all on the same cooperative page. This has all the features of what Naomi Klein calls Disaster Capitalism. You’d never guess it from the website.
What could possibly be the problem with an avowedly ethical body?
To Be Continued next week with the appropriately title Sovereign Individual.
susanne says
Initiating a Globally-Recognized Vaccine Passport, Indonesia’s G20 HWG Meeting Series Welcome More International Visitors
NEWS PROVIDED BY
The Indonesian Ministry of Health
04 Apr, 2022, 18:02 BST
JAKARTA, April 4, 2022 /PRNewswire/ — Assuming the presidency in the upcoming G20 summit, Indonesia has begun the Health Working Group (HWG) meeting series that took place on 28-30 March 2022 in Yogyakarta, Indonesia.
Indonesia’s G20 presidency seeks to harmonize safe and healthy travel procedures worldwide, especially the recognition of COVID-19 vaccine certificates in the wake of the pandemic that ravaged countries globally. The HWG meeting was aimed to foster a dialogue in the health sector between participating countries and synchronize global health protocols.
Continue Reading
Indonesia’s Ministry of Health Discussed Global Standard Health Protocols in the HWG Meetings
Indonesia’s Ministry of Health Discussed Global Standard Health Protocols in the HWG Meetings
The meeting was attended by 70 foreign delegates and 50 local delegates. Delegates who participated in person were Australia, Argentina, the United Kingdom, India, etc., and the World Health Organization (WHO). Meanwhile, those who attended virtually included Canada, France, etc., and international organizations such as the World Bank.
“We need to have synchronized health protocols globally to enable safer international travels and accelerate the social and economic recovery for good,” said Budi Gunadi Sadikin, the Minister of Health of Indonesia.
The HWG meeting has unveiled the initiation to standardize the digital COVID-19 vaccine certificates through a universal verifier made according to the WHO standards. The system is web-based that can be used on all devices. Each country does not need to change the system or the QR codes that are currently used.
Health protocol restrictions differ for every country. For instance, European countries like Denmark, Hungary, etc., have lifted all measures, but some still require a vaccination certificate upon arrival. While Middle East and African countries still require a vaccination certificate or a PCR test.
Each country is given the flexibility to apply necessary health protocols for their countries. However, the procedures are clear and universal thus strengthening the global health architecture and easing traveling across countries.
The synchronization of health protocols is needed to support the interconnectivity of health information. This process is expected to start from the G20 countries and expand to other countries globally.
The second HWG meeting in Lombok in June, will discuss about the global health fund in case of a future pandemic. The last of the HWG series in Bali in November, will discuss about the global medical research.
More information can be accessed at the Indonesia’s Ministry of Health website https://www.kemkes.go.id/.
Photo – https://mma.prnewswire.com/media/1779676/51966371023_bb8af715ed_6k.jpg
SOURCE The Indonesian Ministry of Health
Also from this source
G20 Health Ministers Meeting Delivers Six Key Actions for the…
G20 Health Ministers Meeting Delivers Six Key Actions for the…
G20 ambitious on plan to roll out pandemic fund this year…
G20 ambitious on plan to roll out pandemic fund this year…
susanne says
Here’s the trick –change the names minister No1- issues a lie/policy -change the lie by appointing a different minister No 2. So the first one is not responsible for the change as he is no longer the minister -and neither is the second one resposnisble for what No1 said – he/she makes his own decisions thanks very much with respect to No1…
The Guardian –
Nadhim Zahawi: UK has no plans to introduce Covid vaccine passports – video
1:03
The vaccines minister insisted the government was not considering vaccine passports to allow those who have been vaccinated against Covid-19 to travel internationally. ‘Vaccines are not mandated in the UK … and it would be discriminatory,’ Zahawi told BBC One’s The Andrew Marr Show. ‘We have no plans of introducing a vaccine passport’
Coronavirus live news
Sun 7 Feb 2021 11.39 GMT
susanne says
‘The process is open, transparent blah blah….Have they been popping laughing gas at these jolly gatherings?
Reuters
4 minute readNovember 18, 20227:00 AM GMTLast Updated 4 days ago
Big Pharma may have to reveal government deals in WHO’s draft pandemic rules
By Jennifer Rigby and Emma Farge
LONDON/GENEVA, Nov 17 (Reuters) – Pharmaceutical companies could be made to disclose prices and deals agreed for any products they make to fight future global health emergencies, under new rules that would govern a World Health Organization-backed pandemic accord reviewed by Reuters.
A draft version of the WHO accord, which is being negotiated by the U.N. health agency’s 194 member countries, calls for it to be compulsory for companies to reveal the terms of any public procurement contracts.
It says that public funding for the development of vaccines and treatments should be more transparent,
During the pandemic, many deals governments made with pharmaceutical companies have been kept confidential, giving them little scope to hold drugmakers accountable.
“The process is open, transparent, and with the input from other stakeholders, including any interested stakeholders and public, able to submit comments at public consultations.”
t is at an early stage and likely to change in the course of negotiations with member states and other stakeholders. The draft will be presented to them in full in a meeting on Friday, after being circulated earlier in the week.
The document is vague about what would happen if countries that sign up do not stick to its rules and if companies do not comply. The U.N. agency cannot force companies to follow its rules.
The proposal may face resistance from the drug industry after its meteoric race to develop vaccines and treatments that proved to be critical tools in controlling the virus which has killed more than 6.5 million people worldwide.
Thomas Cueni, director general for the International Federation of Pharmaceutical Manufacturers and Associationsit was important not to undermine how pharmaceutical companies innovate and to protect their intellectual property (IP).
By Jennifer Rigby and Emma Farge
LONDON/GENEVA, Nov 17 (Reuters) – Pharmaceutical companies could be made to disclose prices and deals agreed for any products they make to fight future global health emergencies, under new rules that would govern a World Health Organization-backed pandemic accord reviewed by Reuters.
A draft version of the WHO accord, which is being negotiated by the U.N. health agency’s 194 member countries, calls for it to be compulsory for companies to reveal the terms of any public procurement contracts.
During the pandemic, many deals governments made with pharmaceutical companies have been kept confidential, giving them little scope to hold drugmakers accountable.
A spokesperson for the WHO said it was member states that were driving the current process toward a new agreement.
“The process is open, transparent, and with the input from other stakeholders, including any interested stakeholders and public, able to submit comments at public consultations.”
The agreement is at an early stage and likely to change in the course of negotiations with member states and other stakeholders. The draft will be presented to them in full in a meeting on Friday, after being circulated earlier in the week.
The document is vague about what would happen if countries that sign up do not stick to its rules and if companies do not comply. The U.N. agency cannot force companies to follow its rules.
The proposal may face resistance from the drug industry after its meteoric race to develop vaccines and treatments that proved to be critical tools in controlling the virus which has killed more than 6.5 million people worldwide.
Peter Selley says
David
I’m not sure that EMIG is avowedly ethical, or even claims to be.
Here they are arcanely referring to “Ethical Medicines” which were proprietary medicines that were not supposed to be advertised to the public.
Your correspondent hasn’t told us about another wretched quango – the European Confederation of Pharmaceutical Entrepreneurs (EUCOPE). http://www.eucope.org/
(Yes, it has a “Rare Disease Hub”)
This is what EMIG chair Leslie Galloway said when EMIG joined EUCOPE in 2010: “EMIG has excelled at lobbying on behalf of its members in the UK, and EUCOPE membership will now enable us to influence policy in Brussels without distraction from our core objectives.
annie says
“What can we steal with pride” she said…
https://www.normanfenton.com/
Norman, here, constructively kicks these Data Outfits in to the long-grass :
We analyzed data for specific conditions such as rheumatoid arthritis, diabetes, chronic heart failure, pelvic floor syndrome, multiple sclerosis, and worked with the clinicians to determine causal explanations for observed data so that they can be incorporated into our decision-support systems. So, for example, in the area of trauma we collaborated with surgeons to help improve the decision-making parameters for whether or not to amputate a limb.
For these types of analyses there aren’t massive relevant databases, which is why you need to combine the relatively small amount of available data with the perspective of experienced clinicians. We work with them to build frameworks for effectively eliciting the knowledge needed to make sound decisions. Practical causal models are designed that can be populated with the raw data that we have available, which then provides guidance for those involved in healthcare procedures.
Ben Goldacre Retweeted
DataSavesLives
@DataSaves_Lives
You may know @UniOxford Prof @bengoldacre as the author of ‘Bad Science’ or the initiative to make data from #AllTrials public. But #DYK you can now read his independent report on how the efficient and safe use of #HealthData can benefit patients? READ: https://bit.ly/3aDHyeO
But #DYK
—Witty seemed to be ushering in a glorious new era of openness.
Ben Goldacre, doctor, AllTrials campaign leader, and author of Bad Pharma, which fiercely critiques the industry, called it “a cartwheel moment.”
In an exclusive interview with the Community Forum, Norman Fenton, a veteran UK risk management professor and mathematician explains how the manipulation of pandemic data by scientists, government agencies and mainstream media supports a false narrative with devastating consequences.
https://rwmalonemd.substack.com/p/forum-conversation-norman-fenton
Forum: Norman Fenton, welcome to the Forum Conversation. The analysis you’ve done over the last few years gives incredible insight into what actually unfolded during the pandemic. Before we discuss those findings, can you help us understand how you apply your knowledge to evaluating information outside of your area of expertise, including medical data?
Fenton: For many years I’ve collaborated intensively with clinical experts in different medical domains. For example, before the COVID crisis, I was the principal investigator of a large project funded by the United Kingdom Engineering and Physical Sciences Research Council. Our group uses Bayesian statistical methods, where available knowledge and expertise are combined with data to help improve decision-making for prognosis and diagnosis of chronic medical conditions.
We analyzed data for specific conditions such as rheumatoid arthritis, diabetes, chronic heart failure, pelvic floor syndrome, multiple sclerosis, and worked with the clinicians to determine causal explanations for observed data so that they can be incorporated into our decision-support systems. So, for example, in the area of trauma we collaborated with surgeons to help improve the decision-making parameters for whether or not to amputate a limb.
For these types of analyses there aren’t massive relevant databases, which is why you need to combine the relatively small amount of available data with the perspective of experienced clinicians. We work with them to build frameworks for effectively eliciting the knowledge needed to make sound decisions. Practical causal models are designed that can be populated with the raw data that we have available, which then provides guidance for those involved in healthcare procedures.
We rely on clinicians for checking all aspects of analysis. Although we have worked with pathologists and epidemiologists in understanding the numbers, information about the COVID pandemic doesn’t require a lot of medical knowledge. What was more important was that using only publicly available data enabled us to expose many crucial flaws in the COVID narrative pushed by governments and the mainstream media.
Forum: How did you apply Bayesian analysis to understanding the initial data about testing for the COVID virus?
Fenton: A good example of how we used Bayesian analysis was to answer the question: Do I, or do I not, have the SARS-CoV-2 (COVID) virus? And specifically, if I’m asymptomatic, what is the probability that I might have the virus? Answering this question correctly was the focus of one of our first inquiries.
Suppose that at a given time there is data available suggesting that, in the general population, one in a thousand asymptomatic people were likely to have the virus. Such data was never confirmed of course, the infection rate varied over time, but I will use it to explain the Bayesian reasoning.
If I take a PCR test and it’s positive but I’m not feeling ill, I would want to know if I really have the virus. In other words, if I am one — of the one-in-a-thousand people — who is asymptomatic but carrying the virus, I’d want to know the accuracy of the test. There weren’t any reliable studies about the reliability of the PCR test, but the public was assured these tests were very accurate. Let’s suppose there was only a one-in-a-hundred chance that someone who doesn’t have the virus will test positive — a 1% false positive rate. Then conversely, if I don’t have the virus, there’s a 99% chance of a negative test. With this information most people assumed if you tested positive you almost certainly had COVID. But that is not the case.
Think about a group of 10,000 asymptomatic people getting tested. Because we are assuming one-in-a-thousand asymptomatic people have the virus, that means about 10 of the 10,000 really have the virus. Let’s also assume these genuinely infected people test positive. Then we are left with just under 10,000 people — 9990, who do not have the virus. But a PCR test with only a 1%false positive rate still means that about 100 of these people would falsely test positive. So in total there are 110 people testing positive of whom we know only 10 will actually become ill from the virus.
So, the actual probability that you’ve got the virus if you test positive is closer to 10%. This means that with reasonable assumptions about the underlying infection rate and test accuracy, the PCR test used as a standard for life-impacting decisions and mandates, had a 99% inaccuracy rate for asymptomatic people testing positive.
The confusion lies with the incorrect assumption that even if you don’t have symptoms of the virus, that the possibility of a false positive in the PCR test is only 1%. As more accurate calculations based on reliable data show, that is clearly not the case. To assume these probabilities are equal is known as the fallacy of the transposed conditional. In the courtroom, when DNA evidence is misinterpreted, it’s called the prosecutor’s policy. Those contradictory figures should have raised important questions — it’s not that complicated — it can be presented in a confusing way, but scientists who knew better ignored this data.
Forum: Have the results of that comparative data been confirmed by other studies?
Fenton: We looked at the numbers from a study at Cambridge University where they tested several thousand asymptomatic students for the virus over weeks using pooled PCR testing. And during that period what they found was that very few students tested positive. In fact, over the period, only 43 of the 10,394 tests were positive.
However, unlike what happens in PCR testing in the general population, they did a second confirmatory test on each of the same samples that tested positive. They applied this more reliable, approved standard, where two positives were needed for confirmation; if either one was negative, it meant nobody in the pooled sample was infected. They found 36 out of the 43 samples that had tested positive, when re-tested afterwards, showed negative. So, what they saw was 84% of asymptomatic students showing a positive result on the initial test didn’t have the virus, confirming a very high inaccuracy rate.
Forum: What was the response to your analysis of the Cambridge study? It should have had some impact on policy.
Fenton: We modeled the data properly and were able to get better predictions about the false positive rate and the true underlying infection rate across the asymptomatic population. We wrote a report, vigorously reviewed by our colleagues in data analysis, and then sent it out to various medical publications. We were shocked that it didn’t get to the review stage in any journal. It was the first of our reports rejected with claims that there was insufficient interest or because it was not in their scope. Our analysis of the Cambridge study was even rejected by preprint servers, who have the most tolerant standards, normally publishing anything that isn’t plagiarized.
Forum: This must have been extremely frustrating. How did you account for this unreasonable response?
Fenton: No one wanted to admit or expose that a very significant proportion of asymptomatic testing yielded false positives. Some people simply claimed they knew that what we saw couldn’t be true because they were absolutely sure that the false positive rate of the PCR test is less than 1%. They didn’t want to look at that in the context of what we demonstrated because it contradicted the original driving narrative of the COVID pandemic. Their beliefs were based on a fallacy that drove all pandemic policies.
We can see there was an effort to show an exponential increase in case numbers. The simple extrapolation from what we had shown was that if you test more people — especially a lot of more asymptomatic people — you’ll seem to show more cases, many that actually were false positives. This wouldn’t have helped the arguments for lockdowns, mandates, and later for vaccines. When lockdowns were easing and people were going back to work who were perfectly healthy and didn’t have any symptoms — they still had to get PCR tests. Then again, you have all of the subsequent limiting policies and insistence on vaccination based on what was another huge percentage of false positives.
Forum: There seemed at the beginning of the pandemic a rationale for testing and consideration of how to best protect the public. The media showed body bags on the streets of China, with the implication that if something wasn’t done, this would happen everywhere.
Fenton: We did some appropriate analysis and looked at the infection fatality rate; what the probability of dying was if you contracted the COVID-19 virus. The infection rate and fatality data were gathered from all of the public studies that were available.
We then did a meta analysis, putting all available data together, taking into account that in the early weeks of the pandemic it was mostly the seriously ill, hospitalized patients who were getting the PCR test; and so they were the largest group confirmed as COVID cases. It was obvious how the numbers were being reported incorrectly. If the majority of people with confirmed COVID cases are in hospitals, then the probability of dying with COVID will seem much higher than it actually is, because you’re focusing on a restricted group. This finding uses common sense, not sophisticated data analysis.
Our work concluded that the infection rate — the proportion of people infected — was higher than being presented. But crucially, the infection fatality rate, the possibility that you would die if you were infected with the virus, was much lower than was being reported. Over time, accurate fatality rates only confirmed our work and the conclusions of other studies. The mortality rate was never that high and mostly among those with other pre-conditions. But again, this work was virtually ignored.
Forum: Governments and health authorities admitted that having preexisting conditions put those patients in the highest risk group for hospitalization and death. How did you take that into account?
Fenton: We gathered very good data on this. Through requests based on freedom of information we have indisputable numbers for the UK from over the first two years. And out of 136,000 deaths formally classified as from COVID on their death certificates, about 5000, only 5%, didn’t have at least one other comorbidity. In this group, there were only three children under the age of 20.
There’s another study which looked in detail at the hospital records of all children who entered an ICU with COVID in the first year of the pandemic — about 250 — it was a lower number than a typical flu year. And when they started to examine the numbers, it turned out, there were 38 of those children who ended up dying. Eight of those had their death attributed to COVID — the others were children who had a positive PCR test, but were admitted to the ICU with symptoms of a very serious condition like cancer. And of the eight whose death was attributed to COVID, at least seven had preexisting life-threatening conditions. So essentially, they showed that children under the age of 20 in the UK who died with COVID, actually died from something else. At least in this analysis from the first year, the risk for young people dying from COVID approaches zero.
Forum: Has there been analysis of the figures comparing the percentage of those dying in previous years with the flu and a comorbidity, compared to similar COVID-19 statistics?
Fenton: It is interesting that once COVID-19 started, a lot of the flu data, which had been previously easy to find, suddenly became hard to locate or unavailable. We attempted to get that information without much success, as it would’ve been a very good comparison. There’s certainly anecdotal knowledge. It has always been that the elderly often die with complications of the flu or pneumonia, and it is one of the reasons that they have been considered a high-risk group with COVID.
There was a genuine excess death peak in February and March of 2020, when COVID first arrived. We’re now finding out that was actually due to very poor medical decisions made in respect to the elderly. And I’m not just talking about giving the wrong treatments, such as inappropriately putting patients on ventilators. My clinical colleagues now realize that moving hospitalized elderly patients into care homes where COVID spread like wildfire was catastrophic. The subsequent increase in deaths from the novel COVID virus were likely connected to mismanagement and lack of appropriate treatment.
Forum: Does the data reveal whether the COVID-19 virus actually was more dangerous or deadly, or that as the pandemic went on, it became increasingly so?
Fenton: It appeared dangerous at the beginning, and we still don’t know how much of that was manufactured or due to the catastrophic mismanagement of the elderly. I can’t be certain about early on, but there are very strong indicators that the so-called, subsequent massive waves were greatly exaggerated. For example, in the UK, the second wave, which began in the winter of 2020, was supposed to be much worse in terms of COVID case numbers and fatalities than the first wave.
Again, here it’s important to not just look at numbers, but understand the source of those figures. If you only consider the UK government COVID dashboard, which only issues details of COVID case numbers, hospitalizations and deaths, and recognize they are still dependent on the PCR test, you see a much bigger peak than the first wave. This data was used repeatedly to warn us of the return of deadly conditions.
We looked at other important, independent indicators in the UK. The National Health Service COVID triage dashboard monitored the emergency calls and responses specifically for patients with COVID symptoms. These are people who are forced to call emergency services and get an ambulance because they’ve got worsening COVID symptoms. The numbers reflect genuine healthcare emergencies rather than questionable test results.
That graph clearly shows earlier in 2020 when the virus first hit, there were genuine peaks. But in the winter of 2020 through 2021, there are only ripples of increased emergency calls very similar to a normal flu season.
So there was an initial increase, which can be accounted for by a new powerful variant of the flu that was mismanaged. But the increasing scale claimed by governments can’t be substantiated, and the additional data from the COVID triage dashboard contradicts those inflated figures.
Inadequate and flawed trials
Forum: Can you help us understand what you see as the central flaws of the vaccine trials?
Fenton: I have never run a clinical trial. I’ve only looked at data on clinical trials, so I’m not a clinical trials expert. My experience and expertise is mostly in judging results of observational trials. But there were many obvious problems with the main Pfizer vaccine trial that are just being revealed.
The Pfizer trial was the basis for the 95% effectiveness claim that enabled emergency use authorization for the vaccine. As with all randomized controlled trials it was supposed to be a double blind, placebo-controlled trial. In one of the largest in Argentina, they had an equal number of uninfected patients getting a vaccine or the placebo; 22,000 received the COVID vaccine and 22,000 got a saline injection. Now we know there were all kinds of protocol violations, including people in the placebo group finding out they hadn’t been vaccinated.
A significant number of them dropped out or were given the vaccine. The 95% effectiveness claim was based on the fact that post injection, there were 162 COVID cases among placebo participants compared to just eight among the vaccinated participants. But a much larger number of suspected but unconfirmed cases were fairly evenly spread among those in the vaccine and placebo groups. And a disproportionately small number of vaccinated participants with symptoms received PCR tests compared to placebo participants with symptoms.
Pfizer also excluded participants who developed COVID before their second dose. There were 143 such patients withdrawn. Many of the irregularities occurred at one site in Argentina that had the largest number of participants, almost all of whom were recruited close to the deadline. It is also important to note that no safety outcome was tested in the trial, and to date, more deaths have been recorded overall in the vaccine arm than in the placebo arm.
Not just in Argentina, but in many of the big observational trials conducted after the vaccine rollout, anyone who was vaccinated and who got COVID within two weeks, was classified as an unvaccinated person. The biased rationale behind this decision was that it takes at least two weeks for the vaccine to take effect. This misclassification became accepted as a worldwide practice that distorted the data everywhere.
So, in these observational trials, you’ve got this unbelievable bias in the data, right from the start. Added to that, we know that as in the Pfizer trial, in observational trials a disproportionately small number of vaccinated people did not get routinely tested compared to those who were unvaccinated. Everything done was to justify vaccine rollouts and give subsequent doses.
Forum: Did the pharmaceutical trials combine the results from a number of different countries, adding them all together? And if the Argentinian figures had been removed, would the results have been less conclusive?
Fenton: The Pfizer trial wouldn’t have reached the target without the Argentine site, where there had been mass recruitment just before the deadline. There’s circumstantial evidence that it was set up to obtain the 95% effectiveness figure.
Forum: Fairly soon after these inflated claims of effectiveness, we heard about so-called breakthrough cases. That term seems to have disappeared almost as quickly as it arrived, because it became apparent that all cases are breakthrough cases.
Fenton: They sold us a lie. They told us that if you took the vaccine, you wouldn’t get COVID and you couldn’t transmit it. Now we are finding out that it’s the people who received the vaccine multiple times who are getting COVID more than once, rather than the unvaccinated. We’ve got the numbers showing that in each age group; the vaccinated are disproportionately more likely to get COVID than the unvaccinated.
Forum: The definition of vaccinated has changed over the pandemic. How has that affected data assessment?
Fenton: Despite the shifting definition of the term, we do have data that divides the groups by the number of shots from none to five. The concerted effort to minimize the number of vaccinated people who get COVID was unstoppable. It’s now widely admitted that the vaccine doesn’t stop transmission, confirming actual statistics showing all other analysis was based on skewed results. But when vaccines were being promoted, those of us with expertise who contradicted the interpretation of data were marginalized or ignored. The narrative was framed around an illogical insanity that was widely accepted.
Number of vaccinated people inflated to marginalize the unvaccinated
Forum: There is still an effort to swell the numbers of people who are vaccinated. Is this overt attempt to marginalize the unvaccinated also based on incorrect data?
Fenton: The true proportion of people who are unvaccinated matters in a major way. The Office of National Statistics [ONS] here in the UK made a bizarre claim that in May 2022 only 8% of the adult population is unvaccinated — those never having had one shot. We know that’s not true because the UK Health Security Agency has more reliable data that says it’s closer to 20% of adults in the UK who are unvaccinated; and that’s a conservative number. It may be closer to 30%. When you use this higher figure for unvaccinated, you have a more accurate sample of the population, and in every age group we see that there are more COVID cases among the vaccinated.
Forum: How do you know that the UK Health Security Agency figures are more reliable?
Fenton: Firstly, the ONS data is based on a very unrepresentative subset of the UK population. It only includes people who were both counted in the 2011 census and were also registered with a general practitioner in 2019. That categorizing reduces the adult population of England to from about 49 million to about 39 million. So you’re missing about 10 million adults. This also assumes the census is correct; better estimates would put that missing population at closer to 16 million, a massive number. And a substantial proportion of those in this missing group are certainly unvaccinated.
Even ignoring the children who were born after 2011, you’ve got a huge influx of immigrants coming in. And then those who aren’t registered with a general practitioner are not being pressured by their physician to get vaccinated. It’s overtly a biased sample and not representative.
The UK Health Security Agency is basing their data entirely on the National Immunisation Management Service, which is supposed to have a record of every vaccination, including for COVID. This data can be problematic because it overcounts due to duplicate records — but it doesn’t have a bias that would find lower unvaccinated numbers. From their figures, in May 2022 just under 20% of the adult population was unvaccinated.
Forum: Have these figures been compared publicly?
Fenton: The BBC produced a documentary recently called “Unvaccinated.” They used the ONS figure of 8% of the adult population, presenting this small group as strange outliers who needed to be convinced of their ignorance. Interestingly, the producers contradicted themselves by revealing that to understand attitudes to the vaccines, they had used the ICM survey commissioned by the public broadcaster STV. This was the largest detailed survey about the COVID vaccination program that had been done in the UK. This sampling showed that of 2570 people, 664 were unvaccinated — nearly 26% — which exceeded all other estimates. But the program had a point of view that couldn’t tolerate doubt.
Whether you are a classical statistician or want to do a Bayesian analysis, whichever way you crunch the numbers, the results show a higher population of unvaccinated people than the mainstream narrative suggests. Any analysis of cases or effectiveness changes dramatically when accurate numbers are used.
COVID-19 vaccines don’t work
Forum: The vaccines were promoted as effective in stopping cases. Data and studies that showed the opposite were ignored, although now it has been admitted that the COVID vaccine has never been shown to decrease transmission.
Fenton: What is far worse, there is data that indicates higher vaccination is related to higher rates of infection. A Freedom of Information Act request to the Nova Scotia government in Canada released data that was charted by Jessica Rose. It made this very apparent connection.
Forum: Another country where you compared vaccination and the number of COVID cases was Germany. What did you see there?
Fenton: One argument defending COVID vaccines is that it’s difficult to compare numbers across countries that have very different cultures and healthcare systems. This is partially true, but looking at Germany and its individual states, where they’ve got the same regulations and everybody’s equally encouraged to take the vaccine, this is not a factor.
We compared data from Germany over seven days on COVID cases and COVID vaccine uptake rates. Regional differences in the proportion of people vaccinated could be analyzed. For example, in parts of former East Germany there is more skepticism of the government and we saw much lower vaccine uptake rates.
For each region, when you plot the density of cases against vaccine uptake, you get this remarkable correlation whereby the dense case regions are also the dense vaccine uptake regions. And where there are very few COVID cases you have the least vaccine uptake.
Berlin in particular, shows this very clearly; there’s a much higher proportion of the population vaccinated than other areas, over 62%. And it’s the hotspot for COVID cases. Of course this data uses numbers based on confirmed cases with testing, and as I’ve said, I’m skeptical about testing. Nevertheless, it’s quite a phenomenal finding that’s virtually ignored.
COVID-19 vaccines and mortality
Forum: The emphasis in public pronouncements shifted to how vaccines limit hospitalization and death. Was that ever looked at in studies?
Fenton: Again this is not a complicated analysis. When you plot the vaccination rate for any given country against the COVID mortality rate there is an obvious trend. If the vaccines were working, what we should be seeing is that countries with higher vaccination rates should have lower COVID mortality rates.
What you actually see is the countries with the lowest COVID mortality rates are essentially the African countries with very low vaccination rates. Now the average population age in African countries is lower than elsewhere, so this is a factor, but even among highly comparable countries, those which have high vaccination have higher mortality rates. Australia, for example, currently has the highest COVID mortality rate in the world and claims 96% are vaccinated. There are variables, but there is certainly no correlation showing that vaccinated populations have a lower chance of dying from COVID.
Forum: Yet the number of cases, hospitalizations and death still drives the narrative, even as the pandemic recedes.
Fenton: Despite obvious issues with how numbers are gathered and analyzed, the case rates are still driven by testing that either is unreliable or applied to a narrow group of patients. Either way, the more testing you do, the more cases and hospitalizations you find; and of course, the more deaths you’ll classify as COVID. As cases are massively inflated, subsequent data is useless. Hospitalizations and deaths are real, but many of the COVID cases aren’t. And as has been apparent to anyone who cares to look, most of those who actually have COVID and die are not dying of COVID, they are dying with COVID.
We recognized early on that there was so much manipulation of information that we had to start looking at figures that couldn’t be skewed.
Forum: Your group was one of the first to look at all cause mortality and you recognized some interesting anomalies.
Fenton: Yes, if you want to really understand the safety of the vaccines, you need to analyze all-cause mortality. When we first looked at the ONS data for the UK vaccine program we saw a very strange correlation.
Incredibly, according to the ONS data, as the vaccines were released, there was a significant increase in deaths from other causes than COVID among the unvaccinated. These two statistics should be unrelated. The most likely explanation for this anomaly was that many of those who were dying shortly after vaccination were being classified as unvaccinated. Once the data are adjusted for this misclassification there is no evidence that the vaccines reduce all-cause mortality; rather, there is evidence it may cause an increase, especially in the younger age groups. This should have caused great concern and immediate intervention.
Forum: There is also confirmation of both deaths and serious complications from the vaccines, but these numbers are also ignored. Have you reviewed the data bases like VAERS [Vaccine Adverse Event Reporting System]?
Fenton: As of June 2022, we saw over 1.3 million adverse events showing in the VAERS database, a system widely accepted as flawed for underreporting. Even with these low numbers we knew that there had been about 30,000 deaths and over 165,000 hospitalizations caused by the COVID vaccines. In all previous years since VAERS began recording data, the total number of deaths reported from all vaccinations before COVID was around 10,000. So there are three times as many deaths reported from the COVID vaccine in two years, compared to all deaths from all other vaccines in the reporting over the last 30 odd years. This should be taken as an obvious signal, stopping the COVID vaccine program for reevaluation, but again these numbers are dismissed.
Cartwheel moments…
susanne says
Altruism for the common good may still just about exist but needs to be done by consent.Whatever There’s no way I would put private health info on an app By nature I am a private person ,fundamentally I own it as part of my selfhood and it’s not to be passed on without my consent .There’s nothing noble about betraying a trust which has been in some distant past part of the relationship with health workers and researchers. It is disingenuous to guarantee anonymity or confidentiality – who do they think does the anonymizing. It could be the next door neighbour. The Royal Free some years ago sold millions of records to google plus without peoples’ knowledge, the CEO an ‘ethicist’ claiming that they should have opted out if disagreeing. They had no idea there were opt out options. And it’s still the rub .All People are still not aware they can opt out of sharing medical records for any purpose and the APPs roll out is a mess of misinformation. It is still possible though to obtain paper records with a simple request from the surgery – at the same time as a separate request ie as a ‘right advising them of a decision to opt out of sharing personal medical information including for research. The clinic manager should provide whatever form they use .
This is just one of the campaigns which have lasted of over 15 years of obstruction and resistance to sharing personal medical records and to protect individual privacy.. For people in England and Wales the Patients Association is helpful There’s also a wealth of info re Opting Out and Access to medical records online.
One recent example
The Guardian homeThe Guardian: news
Controversial £360m NHS England data platform ‘lined up’ for Trump backer’s firm
Patients will have no say over records going to Palantir, the software giant run by billionaire Republican backer
Sun 13 Nov 2022 07.00 GMT
An NHS project to incorporate tens of millions of personal digital medical records into one of the biggest health data platforms in the world is to be launched without seeking new patient consent.
Health officials confirmed this weekend the proposed £360m new data platform for England will incorporate the NHS shared care records that track patients across the health and care system.
The American software firm Palantir, which is chaired by the billionaire Donald Trump supporter Peter Thiel, is considered the favourite to win the contract. The firm has hired two senior officials from the NHS and has been advised by Global Counsel, the consultancy firm set up by the former Labour cabinet minister Lord Mandelson.
Ministers have disclosed in parliamentary answers that the patient information project does not require a public consultation before the five-year contract is tendered or additional patient consent. They say the project, called a federated data platform, will help improve care and provide new insights into the nation’s health.
Clive Lewis, the Labour MP, said: “This looks like the contract has been set up to hand it to Palantir. There should be a proper debate about the use of this data so people can make an informed choice.”
Campaigners warn the government risks undermining public trust with plans to “shove hospital data” into a private contractor without proper consultation. They say patients have a “legal right to a say”.
Peter Thiel, a co-founder of PayPal as well as of Palantir.
Palantir was co-founded in 2003 by Thiel, a tech entrepreneur and major donor to the Republican party. It has done extensive work for the intelligence sector and was originally funded by In-Q-Tel, the CIA’s venture capital arm.
Winning the contract would be a coup for Palantir, which was initially contracted to work with the NHS during the Covid pandemic on a nominal fee of just £1. It went on to win a £23.5m contract in December 2020 to provide real-time information on disease prevalence and vaccinations during the outbreak.
Cori Crider, director of the legal campaign group Foxglove, said: “[Palantir] is a company that has worked with border forces, spies and police. They’ve got no place in the NHS.”
The contract notice for the project is waiting to be signed off by the health secretary, Steve Barclay, and “will be issued in the coming weeks”. One official said the new project will help “reduce waiting times, speed up diagnosis and get people home quicker”.
Shared care records, which were launched in April 2021, are being rolled out by integrated care boards, the newly formed partnerships of NHS bodies, local authorities and other organisations.
The records contain a wide range of information including name, address, date of birth, health conditions, medications, medical notes, social care and safeguarding information. The records will be “de-identified” for wider use on the proposed NHS platform for research and analysis to provide better targeted care.
Peter Mandelson’s consultancy Global Counsel has advised Palantir. Photograph: Justin Tallis/Getty Images
Under the proposed new project, the information is not consolidated into one central database, but can be analysed in hundreds of different systems across England. Ministers say information will be transferred from existing datasets that already have “a lawful basis for collection and processing”.
One official said: “Only people with a need to access patient identifiable information in a shared care record will be able to access information pulled from the record for use in the platform.”
Phil Booth, coordinator of medConfidential, which campaigns for confidentiality and consent in health and social care, has described the federated data platform project as “the veins through which patient data would flow”. He said there should have been a consultation and detailed information on the legal justification for the proposed use of patient records.
The NHS has failed to win public trust in previous schemes to use sensitive patient data. A plan to share GP records for research stalled last year after being criticised by campaigners as a “data grab”.
NHS England has already instructed NHS Digital, the national provider of health data and information, to use Palantir’s operating platform called Foundry to collect patient data from acute trusts, including a person’s NHS number, date of birth, postcode and data about admission and inpatient activity. The data is given a pseudonym before it is shared with NHS England. Palantir also has a project working with hospital trusts to reduce waiting lists.
NHS England officials say they will now develop a public pact over safeguards of medical data, outlined in the government’s data saves lives policy paper published in June.
An NHS spokesperson said the contract was an open tender and several companies had expressed an interest. They added that the firm that won the contract would not be permitted access to the data or allowed to share it for its own purposes. It is expected to be awarded by summer 2023.
“Maintaining public confidence in how the NHS handles their personal information is paramount. We have some of the most robust safeguards in the world for data, and worked extensively on these proposals with privacy groups, clinicians and patients.”
The spokesperson added that each trust and integrated care board would determine how they will use their own data platform, and that “no data will be extracted from local shared care records without there being a clear legal basis to do so”.
A Palantir spokesperson said: “We’re incredibly proud of our support for the NHS. Our software helped the NHS to save thousands of lives by powering the Covid vaccination programme. It is now helping to reduce the elective backlog in hospitals.”
The firm says it sells software products and does not monetise or collect personal data.
annie says
“It’s not about the vaccine, it’s not about the virus, it’s about data.”
“What people have to understand is that any other functionality can be loaded onto that platform with no problem at all” stated Naomi Wolf, an author and Rhodes Scholar, predicted that the vaccine passport would eventually track every aspect of people’s lives…
Edward DowdReposted
rwmalonemd
@rwmalonemd
·
15h
Global News: A Global Passport for Vaccines and Carbon Tracking
They’re Coming…
rwmalonemd @ substack
Please share
Global News: A Global Passport for Vaccines and Carbon Tracking
https://rwmalonemd.substack.com/p/global-news-a-global-passport-for?sd=pf
Whіlе ѕоmе ѕuggеѕt thеу аrе lауіng оut thе grоundwоrk fоr thе роtеntіаl реrmаnеnt bаnіѕhmеnt оf ‘undеѕіrаblеѕ’ frоm ѕосіеtу, lеаdеrѕ оf thе Grоuр оf 20 nаtіоnѕ hаvе саllеd fоr а glоbаl ѕtаndаrd оn рrооf оf vассіnаtіоn fоr іntеrnаtіоnаl trаvеl аnd thе еѕtаblіѕhmеnt оf “glоbаl dіgіtаl hеаlth nеtwоrkѕ” thаt buіld оn ехіѕtіng dіgіtаl СОVІD-19 vассіnе раѕѕроrt ѕсhеmеѕ, ассоrdіng tо thе Еросh Тіmеѕ.
“Wе асknоwlеdgе thе іmроrtаnсе оf ѕhаrеd tесhnісаl ѕtаndаrdѕ аnd vеrіfісаtіоn mеthоdѕ, undеr thе frаmеwоrk оf thе ІНR (2005), tо fасіlіtаtе ѕеаmlеѕѕ іntеrnаtіоnаl trаvеl, іntеrореrаbіlіtу, аnd rесоgnіzіng dіgіtаl ѕоlutіоnѕ аnd nоn-dіgіtаl ѕоlutіоnѕ, іnсludіng рrооf оf vассіnаtіоnѕ,” thе G20 јоіnt dесlаrаtіоn rеаdѕ.
This agreement actually was first codified in the spring of 2021. This was covered in a Forbes article, written in May 2021, entitled “Vaccine Passports: World’s 20 Biggest Economies Give Go-Ahead.” This 2021 article states that: “The G20 meeting–where the world’s biggest economies meet to make decisions–took place Tuesday, and members decided to throw their weight behind vaccination passports, as a means of boosting the global travel and tourism economy.”
Somehow, this decision by the G20, made over 1.5 years ago, that vaccine passports would become mandatory within a short period of time managed to escape media attention. Now – of course, it is almost a fait accompli. Of note, many countries have now pledged hundreds of millions, if not billions to the development of such a passport.
G20 Promotes WHO-Standardized Global Vaccine Passport and ‘Digital Health’ Identity Scheme
Epoch Health, Nov 17, 2022
‘Digital Gulag’
Journalist Nick Corbishley, who writes about economic and political trends in Europe and Latin America, has warned that vaccine passports can lead to the implementation of a global digital identity scheme that will threaten privacy and freedom across the world.
“It’s like this checkpoint society. Wherever you want to go, you have to show your mobile phone, your identity … even if it’s just to go into a supermarket or go into a shop,” he told EpochTV’s “Crossroads” program.
Corbishley described the negative aspects of a global digital identification scheme as a kind of “digital gulag” in which people could be “effectively banished from society.”
“That is a terrifying vision,” he said.
World Leaders Agree To Implement Vaccine Passports
Liberty Counsel, Nov 17, 2022
“I cannot say this forcefully enough: This is literally the end of human liberty in the West if this plan unfolds as planned… Vaccine passports sound like a fine thing if you don’t know what those platforms can do. I’m CEO of a tech company, I understand what this platform does. It’s not about the vaccine, it’s not about the virus, it’s about data. And once this rolls out you don’t have a choice about being part of the system. What people have to understand is that any other functionality can be loaded onto that platform with no problem at all” stated Naomi Wolf, an author and Rhodes Scholar, predicted that the vaccine passport would eventually track every aspect of people’s lives and would violate the U.S. Constitution, the Americans With Disabilities Act, and HIPAA.
The Massachusetts Institute of Technology’s Technology Review states, “This new social order will seem unthinkable to most people in so-called free countries. But any change can quickly become normal if people accept it. The new normal will be that we are used to the idea that in some cases being able to move around freely is dependent on us being able to show that we’re healthy. There will be a greater acceptance, I think, of that kind of public health monitoring.”
Liberty Counsel Founder and Chairman Mat Staver said,
“Digital health or vaccine passports along with tracking and tracing apps present a serious threat to freedom. Vaccine passports and tracking apps are about collecting data and control. The vaccine passport is being promoted worldwide to limit a person’s ability to leave home, work, shop, dine, travel, attend a public event, or even worship. COVID is being used to advance this dangerous threat to freedom. We must never accept vaccine passports or tracking apps as the new normal. The implications for freedom are significant.”
From vaccine passports to personal carbon passports: Get ready for CLIMATE-21 fossil fuel virus lockdowns
Does COVID-19 justify the global carbon plans?
Financial Post, Sep 08, 2021
Somewhere deep in the cranium of the climate intelligentsia a seed was planted to produce the florid idea that the global COVID-19 virus could serve as inspiration for humankind to once and for all tackle the looming climate crisis. Mark Carney, the global master of modern corporatism’s climate crusade, dedicates a whole chapter of his book Value(s) to the COVID/climate nexus. “If we come together to meet the biggest challenges in medical biology, so too can we come together to meet the challenges of climate physics and the forces driving inequality.”
That message came clearly this week when 220 medical journals around the world — including the Canadian Medical Association Journal — all of which published the same “editorial” under the headline: “Call for emergency action to limit global temperature increases, restore biodiversity, and protect health.”…
Given the current state of the global pandemic, the assumption that the COVID control experience shows the way forward may strike many as a little premature. It is not obvious that we need to fight the climate with big government interventions, backed by corporations, to totally reshape the global economic and power system.
So here we are. From vaccine passports to digital IDs to tracking “carbon footprints,” these goals are working at “warp speed.”
What is it going to take to stop this globalized version of insanity?
“I’ve never left anything on the field,” he said.
https://abcnews.go.com/Politics/fauci-final-briefing-after-50-years-government-gave/story?id=93754988
The rocket-fuel runs out…
Patrick D Hahn says
Ironically, I discovered “The Prisoner” whilst quarantining with the covid.
The obsession with treating numbers on a sheet of paper, as opposed to actual human beings, has reached its logical conclusion with the covid pandemic, with doctors now being smeared and in some cases fired from their jobs for providing safe and effective medicines proven t save lives and keep patients out of hospital.
Patrick D Hahn says
Today Attorney Jenin Younes tweeted:
“One of my favorite quotes from Fauci’s deposition today: ‘I have a very busy day job running a six billion dollar institute. I don’t have time to worry about things like the Great Barrington Declaration.'”
When I learned Dr. Fauci was being deposed, all I could think to myself was It’s about bloody time.
susanne says
A Very nasty piece of work(ers) Interesting that the Covid Enquiry is already seen as a ‘joke’ and this article coincides with a massive lockdown in China causing great suffering to citizens. Leaders are obviously all chatting to each other . What next?
Understanding and neutralising covid-19 misinformation and disinformation
BMJ 2022; 379 doi: https://doi.org/10.1136/bmj-2022-070331 (Published 22 November 2022)
Cite this as: BMJ 2022;379:e070331
Peer review
Yuxi Wang, research fellow1, John Bye, independent researcher2, Karam Bales, independent researcher and freelance journalist3, Deepti Gurdasani, senior lecturer in machine learning4, Adityavarman Mehta, PhD candidate5, Mohammed Abba-Aji, research fellow6, David Stuckler, professor of social and political science1, Martin McKee,, professor of European public health7
Author affiliations
1Dondena Centre for Research on Social Dynamics and Public Policy, Department of Social and Political Science, Bocconi University, Milan, Italy
2Woking, UK
3National Education Union, London, UK
4The William Harvey Research Institute, Faculty of Medicine and Dentistry, Queen Mary University, London
5University of Leeds, Leeds, UK
6Department of Epidemiology, Boston University School of Public Health, Boston, Massachusetts, USA
7Department of Health Services Research and Policy, London School of Hygiene and Tropical Medicine, London
Correspondence to: Y Wang yuxi.wang@unibocconi.it
Yuxi Wang and colleagues say that the public inquiry on covid-19 must look at who was opposing public health measures and why and should call on public health authorities to engage more effectively with the threats of infodemics
Key messages
Research on the political and commercial determinants of health points to the importance of understanding how evidence is generated and promulgated
During the covid-19 pandemic, several groups have been active in opposing evidence based public health measures
A rapid rise in misinformation and disinformation in digital and physical environments over a short period is called an “infodemic”
Active management of infodemics must form part of a comprehensive pandemic response
Further investigations into the social and public health effects of misinformation groups are needed to inform policy
Much rests on the public inquiry into the UK’s preparedness and response to the covid-19 pandemic (https://covid19.public-inquiry.uk/), with organisations and individuals scrutinised about the advice they gave and the decisions they made. The discussion will likely centre on the science, but it will also consider ideology, in particular the relation between individuals, society, and the state. When is it justifiable to impose restrictions on one group of people to protect others, for example? Some people take the view that it hardly ever is. Throughout the pandemic, some people have opposed almost all measures introduced by governments at Westminster and in the devolved administrations, from the initial lockdown to mask mandates and vaccination certificates. Their messages are similar to those promulgated by adherents to an extreme libertarian philosophy that is now prominent in some sections of society in the United States. Some benefit from generous funding from those opposed to what they term “big government,”12 and some of their messaging has been claimed to include evidence that is fabricated, distorted, or taken out of context.3 Inevitably, given the complex technical issues involved, differentiating fact from fiction can be difficult. One argument asserts that, because everyone has vested interests, including those promoting public health, all sources should be treated the same way. This was set out in the Brussels Declaration, which was drafted with substantial input from the tobacco and alcohol industries.4 But there is now a large body of evidence from researchers working on the commercial determinants of health that contradicts this,5 emphasising the importance of seeing the full picture, including who says what and that which is not said.6
The covid-19 inquiry team has now reported on the consultation about its terms of reference. Those analysing the responses found that 15% of submissions were “campaigns and duplicates.”7 This raises the question of what a campaign is. When different groups submit versions of the same text, the connection is obvious. But other links are less obvious: for example, the BBC reports that UsForThem, which has attracted high level support from politicians in its campaign against restrictions in schools, has links with the Health Advisory and Recovery Team (HART), which in turn has worked on a campaign against children being vaccinated against covid-19.8910 HART, meanwhile, shares members with groups that have opposed vaccination, such as the UK Medical Freedom Alliance and the Children’s Health Defence.
Lady Hallett, an experienced judge and chair of the covid-19 public inquiry, will be accustomed to assessing the veracity and quality of evidence presented. But it can be extremely difficult to get a complete picture of how evidence has been generated, framed, and presented.11 Understanding how the tobacco industry has distorted science, for example, has only been possible by having access to a trove of internal documents released under court order in the United States.12
Leaked online chats among individuals affiliated with some of the groups cited above shed light on links among campaigners against interventions to tackle covid-19 and some politicians, journalists, and members the scientific community.9 If the inquiry is to obtain a full picture of events during the pandemic, then it would benefit from seeing these chats. Fortunately, they are now in the public domain.
Infodemics—a key part of pandemic management
There are two types of misleading information: misinformation and disinformation. They differ in terms of intent; the latter is created with the intention of deceiving. Without additional information, such as the tobacco industry documents mentioned above, it can be difficult to differentiate between them. Their spread—often referred to as an “infodemic”—is now widely acknowledged to be a threat to the global efforts towards ending the pandemic.13 In times of crisis, people are more susceptible to misinformation, disinformation, and conspiracy theories probably because their important psychological needs are unfulfilled, leading to frustration.14
Covid-19 related misinformation and disinformation spread through society from the top down and the bottom up. One study identified politicians, celebrities, and other prominent public figures as sources of covid-19 misinformation and disinformation.15 Even though these sources produced only about 20% of the misleading information, they accounted for 69% of total social media engagement.15 Further evidence on the critical role of politicians in driving covid-19 misinformation and disinformation comes from a comprehensive survey of the traditional and online media landscape.16. The authors concluded that Donald Trump was “likely the largest driver of the covid-19 mis/disinformation ‘infodemic,’” accounting for 37.9% of mentions in the content of identified news articles.16 The Center for Countering Digital Hate, a non-profit organisation based in the UK and the US, analysed over 812 000 posts from Facebook and Twitter in the first quarter of 2021 and identified 12 people responsible for 65% of covid-19 anti-vaccine content, who they dubbed the “disinformation dozen.”17 These people include physicians who are alleged to have turned to pseudoscience, anti-vaccine entrepreneurs promoting alternative treatments, and organisations that have long opposed childhood vaccination.
Misinformation and disinformation manufactured and spread by the public can also generate substantial engagement,1518 so strategies aimed at tackling infodemics should target both top-down and bottom-up spread. In doing so, it is essential to understand the nature of any misinformation and disinformation being promoted as it has the potential to spread fear and possibly cost lives.19 A substantial majority (88%) of the false or misleading claims identified by Simon and colleagues were on social media platforms; television, news outlets, and other websites accounted for 9%, 8%, and 7%, respectively.15 The misleading content that received the highest engagement (29%) typically contained a small degree of accurate information that was re-contextualised and twisted; misinformation and disinformation that included doctored images and videos received the next highest (24%).
Evanega et al looked at 38 million traditional media news articles published in English worldwide. The top three most prevalent misinformation, disinformation, and conspiracy theories related to miracle cures for covid-19, conspiracies involving “deep state” actors paying prominent figures associated with the response to covid-19, and the US Democratic Party manufacturing covid-19 to coincide with Trump’s impeachment. The Wuhan laboratory being a secret bioweapons facility, Bill Gates having foreknowledge of the pandemic, and 5G technology having deleterious health effects were also mentioned.16
A national survey of US adults further investigated the popularity of different types of misinformation. 20 It showed that conspiracy theories endorsed by visible partisan figures received higher levels of support, measured by participant’s beliefs in the misinformation, than non-partisan medical misinformation about the treatment and transmission of covid-19.20 This indicates that people are more likely to believe abstract theories about the nefarious motives of political figures than they are to believe potentially harmful but non-ideological health misinformation.20 Moreover, misinformation and disinformation with a higher degree of generalisability is more likely to get traction than specific information; 29% of Americans believe that the number of covid-19 deaths has been exaggerated, whereas only 13% of Americans support the claim that Bill Gates is responsible for the pandemic.20
What can be done?
The public inquiry must identify lessons that can be learnt before the next pandemic. One such lesson is likely to be the need to develop strategic approaches to tackle disinformation and conspiracy theories. Long before the existence of social media platforms, researchers investigated how to mitigate the effect of exposure to false information.2122 Traditional measures used in the past include exposure to corrective advertising through mass media, content labelling the accuracy of information on consumer products,23 and correcting misinformation and disinformation about certain public services.24
The advent of social media and online platforms has provided a fertile medium for disinformation to flourish. Recent studies have looked at the effectiveness of several types of intervention, including redirection, content labelling, content distribution and sharing, disinformation disclosure, disinformation literacy, advertisement policy, content or account moderation, and security and verification. One literature search examined studies on the effectiveness of different types of countermeasures against disinformation campaigns.25 Looking at outcomes such as beliefs, intended behaviour, knowledge, and observed behaviour, the studies indicate that fact checking can reduce the influence of exposure to false information on people’s beliefs as well as their propensity to share misinformation and disinformation.25 In terms of fact checking interventions, most of the included studies evaluated the effects of disinformation disclosure, which is when the platform informs a user that they have come in contact, shared, or interacted with disinformation; many others studied content labelling using a fact checking tag, funding tag or outdated tag, and some examined interventions that educate users to identify disinformation.25 Although most of these countermeasures are proved effective, they don’t represent the major interventions used by social media platforms in the real world, such as content moderation (removal or suspension of account or content).25
Using randomised experiments based on a hypothetical scenario that includes information that is later refuted, two studies in cognitive psychology identified a “continued influence effect” of misinformation.2627 Even after retraction or warning that certain information was incorrect, the retracted facts continued to stick to memory and shape how some people interpreted events.2627 Schmid and Betsch conducted six experiments to assess how to mitigate the influence of science deniers on an audience.28 The participants were randomly assigned to different levels of rebuttal conditions after being exposed to a public discussion with a science denier of vaccination or climate change.28 The internal meta-analysis across all six experiment shows that not responding to science deniers decreases attitudes to behaviours supported by science (such as vaccination) and reduces intentions to perform these behaviours.28 They also found that providing facts or uncovering rhetorical techniques, such as conspiracy theories, false experts, and impossible expectations, tend to be the most effective and universal tool for science advocates.29 But the risk of backfire effects—where correction of a falsehood can reinforce belief in it among those whose beliefs or political ideologies are threatened by the facts—must be considered.2430
Another approach is psychological inoculation or “prebunking”—exposing people to a weakened dose of a persuasive but false argument to trigger the “immune system.”31 Studies have shown that inducing people to think about accuracy or inoculating against misinformation and disinformation can reduce susceptibility and sharing.30313233 When reading this literature, however, one must differentiate the effects on beliefs, intended behaviour, and knowledge.25 Moreover, the existing literature primarily reports on experimental designs in laboratory or survey settings, with relatively little research on real world behaviours.2634 Empirical studies on the nature of and countermeasures against groups promoting misinformation and disinformation that have gained political and social influence are still lacking.
Finally, legal interventions are being experimented by governments in the real world. A bill in California will allow regulators to punish doctors for spreading false information about covid-19 vaccines and treatments by revoking the license to practise.35 A separate bill seeks to require online platforms such as Facebook to publicly disclose their algorithms on content moderation to determine how disinformation is amplified.36 Given the lack of transparency in allowing academic researchers to examine the potential harms of these platforms, more regulatory actions may be the appropriate course of action.
What should the inquiry focus on?
The public inquiry should do three things. Firstly, it should examine the extent to which groups promoting contrarian messages were able to influence policy. We think it unlikely that they were able to do so directly but, given their links to the media and influential politicians, they should be investigated. Secondly, it should inquire into how effective the government was in countering misinformation and disinformation and whether it drew on cognitive science to devise interventions. Data from the Association of School and College leaders, for example, indicate that eight in 10 schools were targeted by anti-vaccine protesters.37 Anti-vaccine protests also targeted parents and students at school gates. The inquiry should examine whether steps were taken to mitigate the impact of these protests, such as disclosing rhetorical techniques these groups employed to induce fear among parents. Thirdly, to what extent did weaknesses in the government and public health organisations’ (UK Health Security Agency, Joint Committee on Vaccination and Immunisation) messaging (around masks/childhood vaccines) leave space for online misinformation and disinformation to take hold?
Discussion
Historically, science denialism has caused people to refuse preventative measures like immunisation or life saving HIV/AIDS medications, which has distorted attitudes and resulted in years of severe illness and death 28.38 Recent false or misleading covid-19 narratives promoted by some groups to discredit legitimate public health measures, in particular non-pharmacological interventions, may have likewise contributed to preventable illness and death and those responsible must be held legally accountable. Children who could have been protected (as they were in many other European countries) have been unnecessarily exposed to a virus that can have long term effects on multiple organs in the body. Long covid has risen substantially in children and young people39 after consecutive waves of infection. The scientific community and government institutions are not immune to dangerous ideologies and influence operations.
We hope that the information we have included here—on the nature and activities of groups that have opposed measures to reduce transmission of covid-19 and what can be done to tackle them— will be of use to the public inquiry. Fact checking and labelling sources of information clearly have a role. Maybe public health authorities should also do more to expose the methods used by groups promulgating misinformation and devise more effective ways to counter their messaging. The existing Online Safety Bill, recently introduced to the House of Commons, should also explicitly list those who have benefitted financially from the spread of covid-19 related misinformation and disinformation.40 Politicians and parliamentary committees seeking scientific advice must also be transparent about how advisers and experts are chosen, especially when partisan narratives are prominent.
Questions for the public inquiry
To what extent were groups promoting contrarian messages against scientific evidence able to influence policy?
How effective was the government in countering misinformation and disinformation campaigns (and did they draw on cognitive psychology and media studies)?
To what extent did weaknesses in public messaging leave space for online misinformation and disinformation to take hold?
Footnotes
Contributors and sources: The authors have all been involved in researching how denialism and misinformation groups influenced the debate of covid-19 mitigation policies. DS, MM, YW, JB, KB, and DG conceptualised and drafted this paper. AM, MA, and YW gathered academic literature to support the evidence. MM and YW revised the article in response to comments by reviewers. DS is the guarantor of the article.
(https://www.bmj.com/covid-inquiry). The advisory group for the series was chaired by Kara Hanson, and included Martin McKee, although he was not involved in the decision making on the papers that he co-authored. Kamran Abbasi was the lead editor for The BMJ.
References
susanne says
Chinese citizens are now out on the streets they have had enough of oppression in all ways but located now on actions to oppose covid restrictions. We will have to see how many will be killed by Chinese bullets or by covid. If such a vile government caves in due to the by the protests it will hopefully be less likely that other authoritarian governmnts will repeat their previous actions against citizens…
annie says
Dr. Fauci sits for deposition in COVID-19 social media censorship case
https://nypost.com/2022/11/23/dr-fauci-sits-for-deposition-in-covid-19-social-media-censorship-case/
“One thing is clear from the 7 hour deposition of Dr. Fauci today,” Missouri Attorney General and US Senator-elect Eric Schmitt proclaimed on Twitter. “When Fauci speaks — social media censors.”
Fauci’s fall from grace: From orchestrating Covid lockdowns to playing down the lab leak theory and claiming vaccines stopped infections — how one of America’s most revered doctors lost the trust of the nation
Dr Anthony Fauci, 81, stood down today after a mega 54-year stint at the NIH
He has been criticized for U-turning on key policies throughout the pandemic
The top doctor has flip-flopped on masks and over-egged effectiveness of shot
https://www.dailymail.co.uk/health/article-11457313/Faucis-fall-grace-orchestrating-lockdowns-lying-lab-leak.html
Edward Dowd Reposted
WarRoom — Home of ultraMAGA
@WarRoom
·
Senator Ron Johnson’s December Hearings Will Be An “Active Q&A” That Dissects Every Aspect Of The Left’s Lies And Misdeeds Surrounding COVID-19
https://gettr.com/post/p1zg86y2c5a
“He wanted him on”
The Man from U.N.C.L.E. …
annie says
Sydney teen diagnosed with heart condition after first Covid jab
https://www.dailymail.co.uk/news/article-11464097/Covid-Australia-2022-Teen-misses-HSC-pericarditis-jab-reaction-cardiologist-issues-warning.html
Prof Norman Fenton Retweeted
Jikky the mouse
@TheJikky
I’ve seen some absolute crap touted in the last 3 years but this one takes the biscuit.
“Strokes from the vaccine are caused by the stress of having the vaccine” Give me strength.
Look at this joke of a journal
https://twitter.com/TheJikky/status/1594588122159157248
Edward Dowd
@EdwardDowd
·
8h
“ALERT! The cause of all those heart attacks is those who claim that “vaccination” is the cause of all those heart attacks”
References
1. Polack FP
Covid 19 vaccines and the misinterpretation of perceived side effects clarity on the safety of vaccines
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9629406/
A mini review of published literature has been conducted and found that mental stress clearly causes vasoconstriction and arterial constriction of the blood vessels. Therefore, if subjects are panicked, concerned, stressed or scared of the vaccination, their arteries will constrict and become smaller in and around the time of receiving the vaccine. This biological mechanism (the constriction of veins, arteries and vessels under mental stress) is the most likely cause for where there has been blood clots, strokes, heart attacks, dizziness, fainting, blurred vision, loss of smell and taste that may have been experienced shortly after vaccine administration. The extreme mental stress of the patient could most likely be attributed to the fear mongering and scare tactics used by various anti-vaccination groups.
The data presented herein, poses an interesting question, is the fear mongering around vaccines causing many of these perceived side effects by inducing unnecessary stress in vulnerable people? Is the movement and character of anti-vaccination information that may strike fear into the general population causing anxiety and vascular constriction resulting in pathologies such as dizziness, hypernea, fainting, blood clotting, stroke and heart attack? The science discussed here clearly establishes that anxiety and fear causes vasoconstriction disorders, and that a particular movement that is trying to save people with a profound lack of scientific and medical training (the anti-vaccination movement) from vaccine side effects may actually be the entity causing the majority of side effects.
Note for Augusto – ‘managing this alarmism’ …
susanne says
Surprising the psychotherapy industry as allies in the vaccine propaganda haven’t jumped on this. They have plenty of experience of telling people physical symptoms are ‘ all the in the mind ‘ They could , probably are, be making a load of cash out of referrals for vaxx anxiety. Another way of undermining the truth of harms being caused and covered up.
Patrick D Hahn says
Last month I spoke with a woman who was so pro-vax she volunteered for a vaccine trial, and experienced horrendous toxic effects which began on the ride home after the first shot. The doctors diagnosed her with “anxiety due to the covid vaccine,” whatever tf that means.
annie says
Brook Jackson Retweeted
Wittgenstein
@backtolife_2023
Robert F. Kennedy Jr.: Google is a vaccine company
https://twitter.com/backtolife_2023/status/1595835280031981571
The Hill
White House battles pandemic fatigue in vaccine push
Story by Nathaniel Weixel • 7h ago
https://www.msn.com/en-gb/health/other/white-house-battles-pandemic-fatigue-in-vaccine-push/ar-AA14zLOm?ocid=msedgdhp&pc=U531&cvid=a9628cbcbf31447bae148a8ac8c80d19
Pfizer’s CEO rapped by regulator for making ‘misleading’ statements about children’s vaccines
Story by Camilla Turner • 52m ago
https://www.msn.com/en-gb/entertainment/music/pfizer-s-ceo-rapped-by-regulator-for-making-misleading-statements-about-children-s-vaccines/ar-AA14AulX?ocid=msedgdhp&pc=U531&cvid=673a8c4927d04c93babfce79eed1b99d
Pfizer’s CEO has been rapped by the UK’s pharmaceutical watchdog for making “misleading” statements about children’s vaccines, The Telegraph can disclose.
Dr Albert Bourla used an interview with the BBC last December to claim that “there is no doubt in my mind that the benefits, completely, are in favour of” vaccinating youngsters aged five to 11 against Covid-19.
He argued that “Covid in schools is thriving” adding: “This is disturbing, significantly, the educational system, and there are kids that will have severe symptoms.”
The interview was published on Dec 2 – before the vaccine had been approved by Britain’s medical regulator for this age group.
Shortly after the article’s publication, a complaint was submitted to the pharmaceutical watchdog – the Prescription Medicines Code of Practice Authority (PMCPA) – by UsForThem, a parent campaign group which was set up to promote the plight of children during the pandemic.
‘Extremely promotional in nature’
The complaint alleged that Dr Bourla’s remarks about the children’s vaccine were “disgracefully misleading” and “extremely promotional in nature”, arguing that it breached several clauses of the Association of the British Pharmaceutical Industry’s (ABPI) code of practice.
“There is simply no evidence that healthy schoolchildren in the UK are at significant risk from the SARS COV-2 virus and to imply that they are is disgracefully misleading,” they said.
In September 2021, the Joint Committee on Vaccination and Immunisation (JCVI), had advised against a mass roll-out for children aged 12-15, saying the “margin of benefit” was “considered too small” and citing the low risk to healthy children from the virus.
But less than a fortnight later, ministers gave the green light for youngsters to be given a single dose of the Pfizer-BioNTech jab with the UK’s chief medical officers arguing that this would help to keep schools open.
It was not until February 2022 that the JCVI ruled that children aged 5-11 could be offered the vaccine – but ministers said the decision should be left up to parents.
A code of practice panel, convened by the PMCPA, found that Pfizer had breached the code in a number of different ways, including by misleading the public, making unsubstantiated claims, and by failing to present information in a factual and balanced way.
‘Up-to-date scientific evidence’
Pfizer appealed against the findings, strongly refuting UsForThem’s claims that Dr Bourla had breached the code of practice. They argued that his remarks were based on “up-to-date scientific evidence” and could be substantiated by the “publicly available independent benefit-risk assessments”.
Earlier in November an appeal board met to consider their arguments. The breaches of the code relating to misleading the public, making unsubstantiated claims and the lack of balance were upheld.
But the more serious findings – including that Pfizer had brought discredit to the industry, had encouraged irrational use of a medicine and had failed to maintain high standards – were overturned. PMCPA said the full case report will be published in the coming weeks.
A spokesman for Pfizer said they are “committed to the highest levels of integrity in any interaction with the public”.
They added: “We are pleased the UK’s PMCPA Appeal Board found Pfizer to have maintained high standards and upheld confidence in our industry, the two most serious rulings in this complaint from a UK campaign group.
“In the UK, we have always endeavoured to follow the principles and letter of our industry Code of Practice throughout. We will review the case report in detail when we receive it, to inform future activity.
“Throughout the pandemic, our communications have been focused on providing clarity regarding the progress of our science and supporting transparent scientific exchange in the interests of public health.” UsForThem were approached for comment.
Teen’s Death 3 Weeks After Pfizer Vaccine Triggers Investigation
The death last year of a 14-year-old Irish teen three weeks after he received Pfizer’s COVID-19 vaccine has sparked a “considerable investigation” that will include requests to Pfizer for safety information, officials involved in an inquest into the teen’s death said this week.
https://childrenshealthdefense.org/defender/joseph-mcginty-death-pfizer-covid-vaccine-investigation/
In June 2021, The Defender reported on the death of 13-year-old Jacob Clynick just three days after he received the second dose of Pfizer’s COVID-19 vaccine.
The Centers for Disease Control and Prevention declined to investigate Clynick’s death, even though the death was reported to the agency’s Vaccine Adverse Event Reporting System (VAERS).
Between Dec. 14, 2020, and Nov. 11, 2022, there have been nine deaths reported to VAERS following COVID-19 vaccines among children ages 6 months to 5 years, 31 deaths reported among children 5 to 12 years old and 133 deaths among teens 12 to 18 years old.
Last month, Florida Surgeon General Joseph Ladapo, M.D., Ph.D., recommended against mRNA COVID-19 vaccination of males ages 18 to 39 years given the results of a study that found an 84% increase in the risk of cardiac death among young adult males within 28 days of mRNA COVID-19 vaccination.
Since March, Florida has recommended against mRNA COVID-19 vaccination of healthy children and adolescents younger than 18.
On Sept. 30, Sweden announced it would no longer recommend COVID-19 vaccination for children ages 12 to 17 and in Denmark, COVID-19 vaccines are not recommended for anyone under 50 years old.
annie says
Fury at BMJ’s outrageous bid to smear Covid dissenting doctors
https://www.conservativewoman.co.uk/fury-at-bmjs-outrageous-bid-to-smear-covid-dissenting-doctors/
LAST week the British Medical Journal published an article that was extraordinary even by its own very variable standards, entitled Understanding and neutralising Covid-19 misinformation and disinformation.
You will have no problem guessing the content of this patently unscientific piece of propaganda. It was clearly targeted at the doctors and scientists whose evidence-based research and professional observations and medical experiences have given them no option but to challenge and question the official Covid narrative.
The purpose is patent. It attempts to discredit a number of ethically motivated pressure groups and two in particular – the United Kingdom Medical Freedom Alliance (UKMFA) a body which advocates for every individual’s right to informed consent, bodily autonomy and medical choice, and the Health Advisory and Recovery Team (HART) – in that time-honoured Big Brother way that George Orwell so chillingly first depicted. It is clearly designed to ensure that no members of either group get anywhere near the official Covid-19 Inquiry.
The authors of this vile calumny betray themselves immediately with an opening ‘key messages’ doublespeak that could be straight from the pages of Nineteen Eighty-Four:
Research on the political and commercial determinants of health points to the importance of understanding how evidence is generated and promulgated.
During the Covid-19 pandemic, several groups have been active in opposing evidence-based public health measures.
A rapid rise in misinformation and disinformation in digital and physical environments over a short period is called an ‘infodemic’.
Active management of infodemics must form part of a comprehensive pandemic response.
Further investigations into the social and public health effects of misinformation groups are needed to inform policy.
The directors of the UKMFA unsurprisingly infuriated by it, have sent an open letter of complaint to the BMJ’s editor-in-chief, Dr Kamran Abbasi, directing him to the insinuations and unsubstantiated and unreferenced allegations concerning their organisation. They say (putting it more politely than I certainly would) that the article ‘appears to seek to undermine (their) contribution to a critical debate of national importance’. There is no ‘appears’ about it. It does seek to.
The approach of the authors, the letter states, ‘borders on the defamatory, is manifestly unscientific, and falls short of the editorial standards that the BMJ professes to uphold’.
The call by the article’s authors to promote and enforce only one ideology in a totalitarian way, the smearing of named organisations and its stated aim to outlaw any other viewpoint, write the UKMFA directors, should have made it unsuitable for a respected scientific journal such as the BMJ. It is a damning letter. You can read it in full here.
Outrageously the UKMFA were not offered the customary right to reply by the BMJ before the article was published. They have rightly requested an immediate retraction of the article and a published apology.
Further condemnation comes from Dr Elizabeth Evans, the UKMFA’s CEO, shocked by the tone and text of the article and that such an article could ever have been published by the BMJ.
She writes to TCW that ‘it is deeply disturbing that there should be such a blatant push to silence legitimate scientific debate and to seek to exclude opposing voices from the Covid-19 Public Inquiry’.
Dr Evans contends that the main aims and objectives of a public inquiry are to scrutinise and evaluate all the policies that the Government implemented and to do a retrospective full cost-benefit analysis and assessment of any resulting collateral damage:
‘Now is the time to calmly and rationally assess all the arguments and evidence that campaigning groups have tried to present but, due to extreme censorship, were deliberately kept away from the public and political sphere for debate.’
The BMJ article has also come in for a scathing attack from Dr Ros Jones (retired consultant paediatrician, member of HART and convenor of CCVAC, Children’s Covid Vaccine Advisory Committee).
She has written to both the Journal’s Editor and to Yuxi Wang the lead author of the defamatory attack. To Professor Abbasi she points out that the reference they quoted for these three organisations (UsForThem was the third) was from the ByLine Times and the BBC, ‘hardly known for their scientific credentials’. She notes with sorrow that BMJ has been, during the last two years, ‘one of the few journals which appeared to be keeping an open mind on the scientific basis for lockdowns, school closures, masks and random testing’, going on to say ‘It would be a tragedy for science if it closed its pages to anyone questioning potential risks of mRNA vaccines and the wisdom of rolling out a drug to literally billions of people world-wide, in particular children, before completing basic safety investigations’.
To Dr Wang she’s written that as the lead author of a series of letters to the MHRA, the JCVI, the CMOs and the GMC, she was particularly disturbed to find that he classed these as misinformation. Had he actually read any of their publications?
Assuming not, she attached the latest letter, ‘signed by a number of eminent professors and others with huge accumulated experience and academic backgrounds’ which provides links to the previous letters dating back to May 2021 prior to the conditional marketing authorisation for children, with numerous references from high ranking journals.
She concludes, ‘It would be very helpful if you could look through these and provide references for any statements you disagree with’.
Dr Jay Bhattacharya, the renowned professor of medicine, economics, and health research policy at Stanford University in California, has called out the ‘authoritarian nonsense’ proposed by the article’s authors, in a strongly worded tweet, saying it violates ‘key civil rights’ and is ‘inconsistent with long-standing free speech norms in democratic countries’. He is right.
Let’s hope with his voice backing his British colleagues, BMJ will come to their senses.
Jay Bhattacharya
@DrJBhattacharya
The censorship regime that this @bmj_latest article proposes in the name of pandemic response violates key civil rights & is inconsistent with long standing free speech norms in democratic countries. Why is the BMJ promoting dangerous authoritarian nonsense in its opinion pages?
The BMJ
@bmj_latest
·
Nov 23
Active management of infodemics must form part of a comprehensive pandemic response, argue Yuxi Wang and colleagues. Further investigations into the social and public health effects of misinformation groups are needed to inform policy https://bmj.com/content/379/bmj-2022-070331
annie says
The redoubtable Clare and the ‘pithy’ Australia Spectator…
Dr Clare Craig (not one of her impersonators)
@ClareCraigPath
·
28m
“The MHRA have recently approved novel “vaccines” that claim to protect against Omicron BA4/BA5 variants. The evidence used for the basis of these approvals is paper thin and the lack of transparency has worsened recently.”
https://hartgroup.org/what-would-it-take-for-mhra-to-hesitate-on-approvals/
‘Part of their justification for this low bar seems to be their belief in the modelled fantasy of 20 million lives having been saved by vaccination.
Their willingness to believe shoddy evidence from mice data stands in sharp contrast to their unwillingness to listen to the testimony of the vaccine injured and engage with them properly. ‘
What would it take for MHRA to hesitate on approvals?
https://www.hartgroup.org/what-would-it-take-for-mhra-to-hesitate-on-approvals/
It said, “MHRA decided that the benefits are greater than the risks and recommended that this medicine/these medicines can be approved for use.” and “The quality of the product is acceptable, and no new non-clinical or clinical safety concerns have been identified. The benefit/risk balance is, therefore, considered to be positive.”
Again safety was only measured for conditions the manufacturer included in their survey. It was compared to previous doses and then waved through because there were “no new adverse reactions.”
The MHRA closes their statement by declaring this easily refuted belief: “A recent paper in The Lancet journal suggested that COVID-19 vaccines have prevented up to 20 million deaths in the first year of use.” This particular hope is at the level of a fantasy.
Spectator Australia
Covid karma’s gonna get ya
Is demonising the unvaccinated a health hazard?
https://spectator.com.au/2022/11/covid-karmas-gonna-get-ya/
‘I would argue that Covid does kill some of the right people. The anti-vaxxers/maskers are dying in legions,’ tweeted Julie Powell last month. Powell made her name writing a potty-mouthed blog about cooking every recipe in Julia Child’s Mastering the Art of French Cooking which was made into a film starring Meryl Streep as the much more likeable Childs. Powell is the latest person to vent her spleen on the unvaccinated only to die – in her case, ‘suddenly and unexpectedly’ on 26 October of cardiac arrest aged 49. Was it bad luck? Her recent battle with Covid? A vaccine injury? Or Covid karma for her cruel jibes?
Vaccine zealots attacking the unvaccinated have been a feature of the pandemic. ‘Mocking anti-vaxxers’ deaths is ghoulish, yes – but necessary’, wrote Pulitzer Prize-winning columnist Michael Hiltzik in the LA Times in January after the death of Republican Kelly Ernby – an unvaccinated critic of vaccine mandates. Those who ‘deliberately flouted sober medical advice by refusing a vaccine known to reduce the risk of serious disease from the virus, including the risk to others, and end up in the hospital or the grave can be viewed as receiving their just deserts’, Hiltzik moralised. In fact, Ernby died at home of a blood clot while gardening not on a ventilator in hospital but for Hiltzik it didn’t matter, it was a ‘teachable’ moment.
Covid karma is not as ugly. There is no gloating over the untimely deaths of those who attacked or ridiculed the unvaccinated, just a grim sense of foreboding about the true toll of the pandemic’s tarnished silver bullet. Social media captures the outbursts in screen shots that haunt their authors beyond the grave. There are dozens of examples online pinned like butterflies to a board.
They include Willie Garson, star of Sex and the City, who scapegoated the unvaccinated for the failure of the vaccine to end the pandemic. ‘We’ll be wearing masks the rest of our lives because of these f..cking idiots not wearing masks and refusing vaccines’, he ranted, repeatedly calling them ‘stupid ’, ‘morons’, ‘idiots’ and ’selfish and irresponsible’. Eventually, the US Centers for Disease Control published a study in July, showing that Covid vaccines did not stop transmission or infection and vaccinated people were just as infectious as unvaccinated people but it was too late to make much difference to Garson who died of pancreatic cancer on 20 September, just over five months after he was vaccinated.
Early in the pandemic, doctors merrily mocked the vaccine hesitant but sometimes didn’t get the last laugh. Dr. Witold Rogiewicz was vaccinated on Polish television in January 2021. He joked to viewers, ‘I have info for anti-vaxxers and anti-Coviders. If you want to contact Bill Gates you can do this through me. I can also provide from my organism the 5G network.’ A video of the broadcast was taken down when he died suddenly during the night less than three weeks later.
Dr Thomas Flanagan, a plastic surgeon from Ohio was equally jocular after his first jab, tweeting, ‘I didn’t feel the microchip going in but I can hear local radio stations now’. After the second jab he added, ‘The microchip is working just fine.’ But he wasn’t fine. He died three months later, aged 48. His obituary made world headlines because people thought he had written it before his death as a joke. It started, ‘My wild and crazy life has again taken a new, unexpected turn with my shocking and unexpected, yet fabulous, exit.’ It was actually written by his fraternity buddies after his death. He left behind a grieving wife and children.
Dr Sohrab Lutchmedial, a fit Canadian cardiologist, was not so cheery. He wrote that he wanted to punch anyone in the face who persuaded others not to get vaccinated and tweeted, ‘I won’t cry at your funeral’. But it was Lutchmedial who passed away unexpectedly two weeks after his booster in November 2021.
New Zealand rapper Louie Knuxx memorised the faces of those protesting lockdowns in Melbourne so he could ‘punch one of these c..nts in the jaw’. But before he had a chance, he died of a heart attack on 13 August, 2021 while running on his treadmill, age 42.
Darrell Beveridge, the Aussie ‘internet food police’, had an Instagram account called ‘CookSuck’. He enthusiastically supported the exclusion of unvaccinated people from restaurants tweeting, ‘Anti-vaxxers are like people who’ve done a big sh..t in their pants. You’re allowed to do it, it’s very natural, and the bathroom is possibly a scam created by BigToiletTM, but the general public don’t want you in the room with them while they’re eating’. He died suddenly and unexpectedly in June this year aged 41.
Are these deaths related to the Covid vaccines? Without autopsies it is impossible to say. The FDA refuses to release depersonalised reports on people who died post-vaccination but Dr Ute Kruger, a former chief pathologist and a senior physician at Lund University in Sweden said in a recent interview that clinicians often say a patient is unvaccinated when they are vaccinated, and typically don’t do rigorous histopathological testing to detect markers of vaccine injury.
What is apparent in Australia is that along with a dramatic increase in excess deaths due to heart attacks and stroke there has also been an increase above the baseline in cancer deaths that bears watching. All started rising with the rollout of the vaccines. While regulators admit that vaccination can cause blood clots and heart inflammation, they have yet to acknowledge studies that show Covid vaccinations can suppress type I interferon signalling, down regulating cancer surveillance and prevention. It’s only anecdotal evidence at this stage but Kruger says she has noted an increase in cancer since the rollout of the vaccines, a decrease in the average age of those she diagnoses, more people in remission getting aggressive recurrences, and larger tumours occurring in multiple locations.
As the hubristic certainty of the vaccinated wanes, Covid karma is likely to fade away.
All that will be left are the questions about vaccine deaths and injuries hanging in the air, waiting for answers.
susanne says
UKMFA Open Letter to Dr Kamran Abbasi, BMJ Editor in Chief, re Published Article Smearing UKMFA
25/11/22
UKMFA have sent an open letter of complaint to the BMJ Editor in Chief regarding the article linked below, which contains insinuations and unsubstantiated and unreferenced allegations concerning our organisation, and which appears to seek to undermine our contribution to a critical debate of national importance.
There are no responses published as yet
BMJ Article: Understanding and neutralising covid-19 misinformation and disinformation
We evidence that the approach of the authors borders on the defamatory, is manifestly unscientific, and falls short of the editorial standards that the BMJ professes to uphold. We were also disappointed not to have been offered the customary “right to reply” by the BMJ before the article was published. We have requested an immediate retraction of the article and a published apology form the authors.
Please sign up to receive our Newsletter to be notified of new UKMFA Campaigns, Open Letters, Calls-to-Action and important updates.
susanne says
Intended for healthcare professionals
It has taken 6 days for Thebmj to publish this response. They should be making an apology for publishing the disgraceful article in the first place.. It just makes a travesty of
respectful discourse and open debate. The authors shouldn’t need to think that they have to thank Thebmj for allowing their response. Thebmj should defend their decision to publish it.
Covid Inquiry
Understanding and neutralising covid-19 misinformation and disinformation
BMJ 2022; 379 doi: https://doi.org/10.1136/bmj-2022-070331 (Published 22 November 2022)
Cite this as: BMJ 2022;379:e070331
Read our Covid Inquiry series
Dear Editor,
HART comprises a group of volunteer professionals, doctors and scientists unequivocally committed to evidence-based policy making and the precautionary principle. We have no external funding. We believe that high quality science is aided by debate and argument and thank the BMJ for the opportunity to respond. We found the employment of baseless smears, innuendo and guilt by association against HART and others to be disappointing, unhelpful and unprofessional.
We formed HART in response to the dominant narrative that coalesced early during the pandemic before much data was available. Our goal is to test, challenge and question aspects of that narrative in the highest traditions of scientific discourse. We fully support effective and safe vaccines. We are in favour of practical and evidence-based public health measures.
We have publicly raised concerns about vaccination mandates and certificates, the public health impact of lockdown measures, zero-covid targets, masking effectiveness and harms, vaccination of post-infected persons, school closures and vaccinating children to protect adults, amongst other issues that should give pause to serious policy makers planning for future pandemics. We have been surprised to have been met with highly personalised attempts to discredit us rather than mature scientific debate.
We believe many of our concerns will turn out to be justified in the long term, and possibly sooner. As in any scientific debate, we of course recognise that some of our genuine concerns may turn out to have been misplaced as further evidence emerges. We disagree with the proposal that any “contrarian messages” should not “be able to influence policy”. We further disagree with the idea of “revoking the license [sic] to practise” in order to “punish doctors” who raise questions about public health policy, in good faith, in public discourse.
We regard the article as a transparent and quite unsubtle paradigm of a technique they themselves unashamedly promote called “prebunking” (the use of “persuasive but false argument to trigger the [informational] ‘immune system’”). It is littered with evangelism, invective, hysteria and hyperbole constituting, ironically, misinformation in our view. We trust that cooler heads will prevail at the formal inquiry.
For the avoidance of doubt, and with a gentle eye-roll, we point out that we have not made any claims about “bioweapons facilities” in Wuhan, “5G technology having deleterious effects”, or that Bill Gates had “foreknowledge of the pandemic” nor claimed “miracle cures” for covid exist.
HART were among the first to raise concerns about vaccine side effects (including myo/pericarditis, clotting issues and death), overdiagnosis in the post-infectious period and the failure of vaccines to prevent infection. These were all smeared as “misinformation” – all are now widely accepted as true.
We deplore abandoning core ethical principles such as adults having a duty to protect children, informed consent and bodily autonomy. We do not understand why the expert formal UK pandemic plan, effectively implemented by Sweden, was swiftly abandoned and replaced by snap decision-making predicated on panic and fear.
We recall the Health Secretary stating in the House of Commons: “This vaccine will not be used on children, it hasn’t been tested on children and the reason is that the likelihood of children having significant detriment if they catch covid is very very low.” [1]
We are not sure why this sensible policy was subsequently ditched.
In conclusion, we again thank the BMJ for the opportunity to refute the groundless allegations made in the article above and invite readers to draw their own conclusions as to the credibility of authors who struggle to evidence many of the, frankly, wild claims they make against HART group and others.
Reference:
1 Covid-19 Update – Hansard – UK Parliament. https://hansard.parliament.uk/Commons/2020-11-10/debates/FB5296EC-628D-4… (accessed 27 Nov 2022).
Competing interests: No competing interests