The Pandemic of Disinformation Through the Eyes of a Cardiologist – Part 1

shortlink: https://t.ly/gbaa

Aseem Malhotra, a controversial cardiologist, vaccinated, convinces his patients to get vaccinated against Covid in particular. He fully supports the 'narrative', until his father dies unexpectedly and inexplicably. It turns out heart failure, exactly Malhotra's specialization. Even though he had recently examined his father. He describes the search that follows in a Case Study, published today. Because it is such an accessible and well-researched (peer reviewed) story, I share it here in Dutch. I also realize that this is only about heart problems. I suspect that we will also see similar stories in other fields: cerebral infarctions, flare-up of cancer, neurological problems... For the time being, it remains a guess.

Below is the translation of the two articles from The Journal of Insulin Resistance. The 48 references refer to the original english article. There you will also find the document and research details, PDF/XMS/EPUB versions, contact addresses etc. If you read English well, please go there. This is Part 1 only. For Part 2 of the paper look here, including the text of this article, also as a Dutch version.

Fighting the COVID-19 mRNA vaccine misinformation pandemic with true evidence-based medicine – Part 1

Vaccines save lives

The development of safe and highly effective vaccines in the second half of the 20th century is one of the greatest achievements of medicine. The prominent scars on my left arm are a constant reminder of the success of our ability to contain some of the deadliest diseases like smallpox, tuberculosis (TB), measles, mumps and rubella, to name a few. It is estimated that the traditional vaccines together save about 4 to 5 million lives per year¹. The greatest success of vaccination was the global eradication of smallpox, which had a mortality rate of 30%.²

In other words, nearly one in three people who contracted smallpox died. The development of a safe and effective vaccine after much trial and error led to 95 out of 100 people being protected from symptomatic smallpox infection and immunity lasting five years, completely eradicating the virus in the seventies. Similarly, one dose of measles vaccine is said to be "95% effective." What is meant by that? Most people assume that 95 out of 100 people who get the inoculation are protected from symptomatic infection and transmission and also have long-term immunity. Similarly, when exposed to chickenpox, only five out of 100 vaccinated children will contract this disease.

Vaccines are also among the safest interventions in the world compared to most drugs used in the treatment of chronic diseases, as we should expect, since they are administered to prevent something in healthy people and not to treat a disease. Therefore, it was good news that in the summer of 2020, several pharmaceutical companies, including Pfizer and Moderna, announced the results of their two-month randomized controlled trial, which showed that they had developed a vaccine with an effectiveness of more than 95% to prevent infection of what was at the time the most circulating strain of the coronavirus 2019 (COVID-19).

The experience of a doctor

As a volunteer at a vaccination center, I was one of the first to receive two doses of Pfizer's mRNA vaccine in late January 2021. Although I knew my individual risk of COVID-19 was small at age 43 with optimal metabolic healtl1, the main reason I took the jab was to prevent transmission of the virus to my vulnerable patients. In early 2021, I was both surprised and concerned by some of my vaccine-reluctant patients and people in my social network who asked me to comment on what I considered mere "anti-vax" propaganda at the time.

I was asked for Good Morning Britain after a film director, Gurinder Chadha, Order of the British Empire (OBE), who was previously wary of vaccines and was also interviewed, explained that I had convinced her to take the jab.

But a few months later, a very unexpected and extremely harrowing personal tragedy happened that would be the beginning of my own journey into what would ultimately prove to be a revelation and eye-opening, so profound that after six months of critical review of the data itself, I spoke with leading scientists involved in COVID-19 research, vaccine safety and development, and with two investigative journalists, have slowly and reluctantly concluded that, contrary to my own initial dogmatic beliefs, Pfizer's mRNA vaccine is not nearly as safe and effective as we initially thought. This critical assessment is based on the analytical framework for practicing and teaching evidence-based medicine, making specific use of individual clinical expertise and/or experience using the best available evidence and taking into account the patient's preferences and values.

A case study

Case studies are a useful way to convey complex clinical information and can reveal useful data that would be lost or not made clear in the summary results of a clinical trial.

On July 26, 2021, my father, Dr Kailash Chand OBE, former deputy chairman of the British Medical Association (BMA) and its honorary vice-chairman (who had also taken both doses of the Pfizer mRNA vaccine six months earlier) went into cardiac arrest at home after chest pain. A later investigation found that a significant delay in the ambulance likely contributed to his death.³ But I found his post-mortem findings particularly shocking and inexplicable. Two of his three major arteries had severe blockages: 90% blockage in his left vein and 75% blockage in his right heart vein. Considering he was an extremely fit and active 73-year-old man, who had walked an average of 10-15000 steps a day during his entire lockdown, this was a shock to everyone who knew him, but especially to me. I knew his medical history and lifestyle in detail. My father, who had been an avid athlete all his life, was fitter than the vast majority of men his age. Since the previous heart scans (a few years earlier, which had revealed no significant problems with perfect blood flow through his arteries and only slight ramps) he had stopped sugar, lost belly fat, reduced the dose of his blood pressure pills, had started regular meditation, reversed his prediabetes and even massively lowered his triglycerides in the blood, which significantly improved his cholesterol profile.

I couldn't explain his postmortem findings, especially since there was no evidence of a real heart attack but with severe blockages. This was exactly my own special area of research. That is, how to slow and even reverse the progression of heart disease. In my own clinic, I successfully prescribe a lifestyle protocol to my patients based on the best available evidence on how to achieve it. In fact, I co-authored a highly impactful peer-reviewed paper with two internationally renowned cardiologists (both editors of medical journals) on shifting the paradigm on how heart disease can be most effectively prevented through lifestyle changes.⁴ We highlighted the fact that coronary artery disease is a chronic inflammatory condition exacerbated by insulin resistance. Then, in November 2021, 1 was alerted to a peer-reviewed abstract published in Circulation, with disturbing findings. In more than 500 middle-aged patients under regular follow-up, using a predictive scoring model based on inflammatory markers strongly correlated with heart attack risk, the mRNA vaccine was associated with a significant increase in the risk of a coronary event within five years from 11% before the mRNA vaccine to 25% 2-10 weeks after the mRNA vaccine. An early and relevant criticism of the validity of the findings was that there was no control group, yet even if it was partially accurate, that would mean there would be a big acceleration in the progression of coronary artery disease, and more importantly, the risk of heart attack, within months of taking the vaccine. I wondered if my father's Pfizer vaccination, which he had received six months earlier, could have contributed to his unexplained untimely death and so I began to critically review the data.

Doubts about the data

I remember a fellow cardiologist informing me, to my surprise at the time, that he had decided not to take the vaccine for a number of reasons, including his personal low background risk of COVID-19 (see Table 1)⁶ and concerns about unknown short- and longer-term damage. One thing that troubled him about Pfizer's crucial mRNA study, published in The New England Journal of Medicine, was the data in the supplement, specifically that there were four cardiac arrests in those who took the vaccine, versus only one in the placebo group. ⁷

These figures were small in absolute terms and did not achieve statistical significance in the study, suggesting that it may just be a coincidence, but without further studies it was not possible to rule out that this is a true causal relationship (especially without access to the raw data), in which case it could cause a wave of cardiac arrests once the vaccine is distributed to tens of millions of people around the world.

In terms of effectiveness, headlines around the world made very bold claims of 95% effectiveness, with the interchangeable use of "effectiveness" and "effectiveness" obscuring the stark difference between controlled trials and real-world conditions.⁸ It would be understandable to the lay public and doctors to interpret this as meaning that 95% of people would be protected from infection if 100 people were vaccinated. Even the director of the Centers of Disease Control (CDC), Rochelle Walensky, recently admitted in an interview that it was the first reports from CNN that made her optimistic that the vaccine would significantly stop transmission and infection, but it later turned out that this was far from true for the COVID-19 vaccines.⁹ The original trial found that a person was 95% less likely to contract the fall variant of COVID-19. This is known in medical terms as relative risk reduction, but in order to know the true value of a treatment, one must consider for that person how much their individual risk has been reduced by the intervention – i.e. the absolute individual risk reduction.¹⁰

Importantly, the trial results indicate that the vaccine only prevents someone from getting a positive test with symptoms, and that the absolute risk reduction for that is 0.84% (0.88% reduced to 0.04%). In other words, if 10,000 people had been vaccinated and 10,000 had not, for every 10,000 vaccinated people in trial, 4 people would have tested positive with symptoms, compared to 88 who had not been vaccinated. Even in the unvaccinated group, 9,912 out of 10,000 (more than 99%) would not have tested positive during the trial period. Another way to express this is that you would have to vaccinate 119 people to prevent one such symptomatic positive test (which is supposed to indicate an infection, which in itself is potentially misleading, but beyond the scope of this article).

This absolute risk reduction (0.84%) is extremely important for doctors and patients to know, but how many of them were told this when they got the jab? Transparent communication about risks and benefits of each intervention is a core principle of ethical, evidence-based medical practice and informed consent.¹¹

The Academy of Medical Royal Colleges made this clear in an article published in the BMJ in 2015.¹²A co-author at the time was also the then president of the General Medical Council. Gerd Gigerenzer, the director of the Max Planck Institute, even stated in a 2009 World Health Organization (WHO) bulletin: "It is an ethical imperative that every doctor and patient understands the difference between relative and absolute risks to protect patients from unnecessary fear and manipulation."¹³

Contrary to popular belief, the study did not show a statistically significant reduction in serious illness or COVID-19 mortality from the vaccine during the six months of the study, but the actual number of deaths (attributed to COVID-19) is still important to note. There were only two deaths from COVID-19 in the placebo group and one death from COVID-19 in the vaccine group. Looking at all-cause mortality over a longer period of time, there were actually slightly more deaths¹⁴in the vaccine group (19 deaths) than in the placebo group (17 deaths). Also noteworthy was the extremely low number of cases of COVID-19 disease identified as severe in the placebo group (nine severe cases out of 21,686 subjects, 0.04%), indicating a very low risk of serious illness, even in areas chosen for the study because the infection was thought to be common.

Finally, the trials in children did not even show a reduction in symptomatic infections, but used the surrogate measure of blood antibody levels to establish efficacy, although the link between the antibody levels caused by the Wuhan spike vaccine and protection against infection is weak at best. The Food and Drug Administration (FDA) website states that:

The results of the currently permitted SARS-COV-2 antibody tests should not be used to evaluate a person's level of immunity or protection against COVID-19 at any time, and certainly not after the person has received a COVID-19 vaccination.¹⁵

Now that we know what the published trial did and did not show in terms of vaccine efficacy, we can try to extrapolate what the effect of the vaccine would be in reducing the mortality rate or other negative consequences of the virus. If there is a 1 in 119 chance that the vaccine will protect you from symptomatic infection by ancestral variants, then in order to find protection against mortality, this figure (11 = 119), must be multiplied by the number of infections leading to one death for each age group. This would result (up to two months after the vaccination) in the absolute risk reduction (before death) of the vaccine. For example, if my risk of dying from Delta at age 44 (should I become infected with it) is 1 in 3,000, then the absolute risk reduction of the vaccine that protects me from death is 1 in 3,000 multiplied by 119, so 1 in 357,000.

Of course, even for the people who become infected, the vaccination can provide some protection against death. Observational data can be used to calculate how many people need to be vaccinated to prevent a COVID-19 death. A comparison of population mortality rates¹⁶ for example, during the Delta wave indicates that 230 over-80s need to be vaccinated to prevent one death during that period, while that number rises to 520 for 70-year-olds and 10000 for 40-year-olds (see Table 2 and Figure 1 ¹⁷).

However, these figures are distorted by inaccuracies in the measurement of the size of the unvaccinated population. As also noted in a recent editorial by John Ioannidis in BMJ evidence-based medicine, the vaccine's efficacy derived from non-randomized trials may be "spurious," with the bias caused by "pre-existing immunity, misclassification of vaccination, differences in exposure, testing, confusion due to disease risk factors, hospitalization decisions, differences in treatment use, and attribution of death".¹⁸

These figures refer to the entire population of England and do not necessarily apply to the healthy population; More than 95% of the deaths involved people with pre-existing conditions.¹⁹ It is also important to note that the vaccinated and unvaccinated populations differ from each other in other ways, which can skew mortality rates. For example, the unvaccinated are more likely to belong to a lower socioeconomic population, putting them at greater risk of serious illness or death if infected.

Professor Carl Heneghan, the director of the Centre of Evidence Based Medicine at Oxford, has explained his own clinical experience with the bias of healthy users. Some of his own patients who ended up in intensive care unit (ICU) with COVID-19 (classified as unvaccinated) did not take the vaccine because they were already suffering from a terminal illness.

Given these limitations, the above figures are likely to be an overestimation of the individual benefit of vaccination; Discussing such uncertainties openly and honestly is an essential part of shared decision-making.

What should be part of the discussion about shared informed consent when someone is considering taking the jab is something along these lines: Depending on your age, hundreds or thousands of people like you should be injected to prevent one person from dying from the Delta variant of COVID-19 over a period of about three months. For people over 80, this number is at least 230, but it rises the younger one is, to at least 2,600 for people aged 30 and over, 10,000 for people aged 40 and 93,000 for people aged 18 to 29. For omicron, which has been shown to be 30%-50% less lethal, that means significantly more people need to be vaccinated to prevent one death. How long the protection actually lasts is unknown; Currently, in some countries, boosters are recommended after only 4 months.

But how many people have had a conversation even close to such a statement? Not to mention the known, unknown and not yet fully quantified damage.

While many have proposed that omikron is intrinsically less lethal (supported by the observed molecular differences between omikron and the Wuhan-type virus), the immunity built up from previous exposure to protect against severe disease is also likely to be relevant to some extent. The crucial point is that, whether viral or immune-related, the milder nature of omikron is evident in the unvaccinated and therefore the reduction in mortality should not be attributed to vaccines.

What are the disadvantages?

Concerns have already been raised about the underreporting of adverse events in the clinical trials for the COVID-19 vaccines. Investigating medical reporter Maryanne Demasi analyzed the various ways the pivotal mRNA tests failed to account for serious damage.²⁰ Not only were trial participants limited to the types of side effects they could report on their digital apps, but some participants who were hospitalized after the inoculation were taken out of the trial and not reported in the final results. After two months in the pivotal trials, the FDA allowed vaccine companies to offer the vaccine to subjects in the placebo group, essentially torpedoing any chance of proper record of side effects from then on and forcing a reliance on pharmacovigilance data.

Such data shows that one of the most common damage caused by the mRNA COVID-19 vaccine is myocarditis. A study in several Scandinavian countries showed an increased risk of mRNA vaccination relative to background, especially in young men.²¹ Authorities have repeatedly claimed that myocarditis is more common after COVID-19 infection than after vaccination.²² However, research data showing that vaccination reduces the risk of myocarditis in later infection is elusive, and in fact, the risks may be additive. The incidence of myocarditis skyrocketed from spring 2021, when the vaccines were rolled out to the younger cohorts who had remained within normal levels throughout the year before, despite COVID-19,²³with the most recent evidence, a paper from Israel²⁴found that the infection itself, prior to the vaccine rollout, did not increase the risk of myocarditis or pericarditis from COVID-19, strongly suggesting that the increases observed in previous studies were due to the mRNA vaccines, with or without COVID-19 infections as an additional risk in the vaccinated.²⁴

Indeed, this reflects my own clinical experience advising and guiding several patients in the community who presented with a clear suggestion from the history of myocarditis after mRNA vaccination, but who were not necessarily unwell to be hospitalized. A very fit lady in her 50s developed fatigue and shortness of breath with exercise a few weeks after her second Pfizer injection. An echocardiogram showed severe impairment of her left ventricular function. Another 30-year-old lady developed similar symptoms with disturbing palpitations within a few days of her second injection; an ultrasound also showed a slight deterioration in left ventricle function, and a subsequent MRI scan of the heart showed several areas of lategadolinium elevation, a feature seen on the scan that corresponds to damaged heart tissue, and since heart cells cannot be replaced, this is likely to have long-term consequences.

Although vaccination-induced myocarditis is not often fatal in young adults, MRI scans show that about 80% of those who are hospitalized have some degree of myocardial damage.^25,26It is as if one gets a small heart attack and suffers a – probably permanent – injury to the heart muscle. It is uncertain how this will play out in the longer term, including whether and to what extent this will increase the risk of poor quality of life or possibly more serious cardiac arrhythmias in the future.

A number of reports, depending on age, have yielded rates of myocarditis ranging from 1 in 6,000 in Israel²⁷ up to 1 in 2,700 in a study in Hong Kong involving male children and adolescents aged 12-17.²⁸Most epidemiological studies that have been conducted have measured cases of myocarditis diagnosed in a hospital setting, and do not pretend to be a complete measurement of more mild cases (from which long-term damage cannot be excluded). Moreover, underreporting of adverse events is the scourge of pharmacovigilance data.²⁹

The UK relies on the Medicines and Health Regulatory Agency's (MHRAs) "Yellow Card" reporting system,³⁰ dat verre van toereikend is voor een snelle uitrol van een gloednieuw product. Het ontdekte de stollingsproblemen die leidden tot de intrekking van het AstraZeneca-product in april 2021 voor jongeren pas nadat in het Verenigd Koninkrijk 9,7 miljoen doses waren toegediend³¹; in Denemarken daarentegen werd het probleem ontdekt nadat slechts 150.000 doses waren toegediend.³²

In het Verenigd Koninkrijk zijn sinds de verspreiding van het vaccin bijna 500.000 meldingen van ongewenste voorvallen geregistreerd (via het gele kaartsysteem) in verband met de mRNA COVID-19-vaccinaties, waarbij meer dan 150.000 personen betrokken waren. In termen van het aantal meldingen per persoon (d.w.z. die ten minste één dosis heeft ontvangen) laten de cijfers van de MHRA zien dat ongeveer 1 op 120 personen een waarschijnlijk ongewenst voorval heeft dat meer dan licht is.³⁰De MHRA is echter niet duidelijk over het percentage en maakt bovendien geen onderscheid tussen ernstige ongewenste voorvallen. Niettemin is dit niveau van meldingen ongekend in het moderne medische tijdperk en gelijk aan het totale aantal meldingen dat in de eerste 40 jaar van het meldingssysteem van de gele kaart (voor alle geneesmiddelen – niet alleen vaccins) tot 2020 is ontvangen.³³ Ter vergelijking: voor het vaccin tegen mazelen, bof en rode hond (MMR) bedroeg het aantal meldingen per gevaccineerde persoon ongeveer 1 op 4.000, meer dan dertig keer minder vaak dan de 1 op 120 meldingen van de gele kaart voor ontvangers van een COVID-19-vaccin.³⁴ Noorwegen scheidt wel de gemelde ernstige bijwerkingen en toont een percentage van ongeveer 1 op 1000 na twee doses BioNTech /Pfizer mRNA-product die leiden tot ziekenhuisopname of levensveranderend zijn.³⁵

Een andere, meer bruikbare informatiebron (vanwege de gedetailleerdheid van elk rapport dat aan het publiek ter beschikking wordt gesteld) is het Vaccine Adverse Effect Reporting System (V AERS) van de Verenigde Staten (VS). Net als bij het systeem van het VK is het aantal meldingen – waaronder ernstige – in verband met COVID-19-vaccins volkomen ongekend. Vanaf 02 maart 2022 zijn bijvoorbeeld meer dan 24.000 sterfgevallen geregistreerd in VAERS; 29% daarvan deed zich voor binnen 48 uur na de injectie en de helft binnen twee weken. Het gemiddelde meldingspercentage vóór 2020 bedroeg minder dan 300 sterfgevallen per jaar. Een vaak gegeven verklaring hiervoor is dat de uitrol van het COVID-19-vaccin ongekend omvangrijk is; dit gaat echter niet op, aangezien de Verenigde Staten (in ieder geval de afgelopen tien jaar) jaarlijks 150 miljoen -200 miljoen vaccinaties hebben toegediend. Een andere kritiek op V AERS is dat “iedereen een melding kan maken”, maar een analyse van een steekproef van 250 vroegtijdige sterfgevallen wees uit dat de overgrote meerderheid bestaat uit meldingen door ziekenhuizen of artsen³⁶Het bewust indienen van een vals VAERS-verslag is daarbij een overtreding van de federale wetgeving waarop een boete en gevangenisstraf staan.³⁷

Aangezien VAERS is opgezet om vroegtijdige signalen van potentiële schade voor nieuwe vaccins te genereren, en daarbij voor verscheidene producten een rol heeft gespeeld, lijkt het pervers om het nu pas als onbetrouwbaar te bekritiseren, terwijl er geen veranderingen in de werking ervan lijken te zijn aangebracht.

Geschat wordt dat de ernstige bijwerkingen die officieel worden gemeld in feite een grove onderschatting zijn, en dit moet in gedachten worden gehouden bij de bovenstaande opmerkingen over VAERS-rapporten. In een artikel van David Kessler (voormalig FDA-commissaris) worden bijvoorbeeld gegevens aangehaald waaruit blijkt dat slechts 1% van de ernstige bijwerkingen aan de FDA wordt gemeld.³⁸Evenzo wordt in verband met de regeling voor de gele kaart in het Verenigd Koninkrijk geschat dat slechts 10% van de ernstige bijwerkingen wordt gemeld.^39,40 Een recente voorpublicatie die mede is geschreven door enkele van de meest betrouwbare medische wetenschappers ter wereld in verband met de transparantie van gegevens voegt geldigheid toe aan de geneesmiddelenbewakingsgegevens. Door gegevens van de websites van de FDA en Health Canada te raadplegen en resultaten te combineren van tijdschriftartikelen waarin de Pfizer- en Moderna-proeven werden gepubliceerd, concludeerden de auteurs dat het absolute risico op een ernstig ongewenst voorval van de mRNA-vaccins (een percentage van één op 800) aanzienlijk hoger lag dan het risico op ziekenhuisopname bij COVID-19 in gerandomiseerde gecontroleerde proeven.¹⁷

Wat VAERS en andere meldingssystemen (met inbegrip van de nog te raadplegen en onafhankelijk te evalueren ruwe gegevens van gerandomiseerde gecontroleerde proeven) zullen missen, zijn potentiële middellange- tot langetermijnschade die noch patiënten noch artsen automatisch aan het geneesmiddel zullen toeschrijven. Als het mRNA-vaccin bijvoorbeeld binnen enkele maanden het risico op een coronaire aandoening verhoogt (wat waarschijnlijk een factor was die bijdroeg tot de plotselinge hartdood van mijn vader), dan zou dit het aantal aandoeningen ver na de eerste paar weken van de prik verhogen, maar het is zeer onwaarschijnlijk dat dit later aan het vaccin wordt toegeschreven en dus wordt gemeld.

Het is leerzaam om op te merken dat volgens gegevens van de ambulancedienst er in 2021 (het jaar van de uitrol van het vaccin) ongeveer 20 000 (-20% stijging) extra oproepen voor out-of-hospital hartstilstand waren vergeleken met 2019, en ongeveer 14.000 meer dan in 2020. Gegevens die in het kader van de wetgeving inzake vrijheid van informatie zijn verkregen van een van de grootste ambulance trusts in Engeland suggereren dat er van november 2020 tot maart 2021 geen stijging was, en daarna is de stijging onevenredig sterk bij jongeren waargenomen.⁴¹ Dit is een enorm signaal dat zeker met enige spoed moet worden onderzocht.⁴²

Evenzo werd in een recent artikel in Nature een toename van 25% aangetoond van zowel acute coronaire syndromen als hartstilstanden in de leeftijdsgroepen van 16 tot 39 jaar die significant geassocieerd waren met toediening van de eerste en tweede dosis van de mRNA-vaccins, maar geen verband v.1 met COVID-19-infectie.⁴³ De auteurs stellen dat:

De bevindingen geven aanleiding tot bezorgdheid over door vaccins veroorzaakte onopgemerkte ernstige cardiovasculaire bijwerkingen en versterken het reeds vastgestelde causale verband tussen vaccins en myocarditis, een frequente oorzaak van onverwachte hartstilstand bij jonge mensen. (p. 1)

De verontrustende bevindingen in dit artikel hebben geleid tot oproepen tot intrekking. In het verleden zouden wetenschappers met een andere kijk op hoe gegevens moeten worden geanalyseerd, een artikel met afwijkende aannames en interpretatie hebben gepubliceerd voor discussie. Nu proberen ze te censureren.

Er is nog veel meer bezorgdheid geuit over mogelijke schade van de vaccins op middellange tot lange termijn. Hoewel sommige van deze zorgen hypothetisch blijven, kan het een ernstige vergissing zijn zich alleen te concentreren op wat meetbaar is en niet op het bredere plaatje, vooral voor jongeren.

Wat zou het schademechanisme kunnen zijn?

Bij “conventionele vaccins” wordt een inert deel van de bacterie of het virus gebruikt om het immuunsysteem “op te voeden”. De immuunstimulans is beperkt, gelokaliseerd en van korte duur. Voor de COVID-19-vaccins is aangetoond dat het spike-eiwit continu (en in onvoorspelbare hoeveelheden) wordt geproduceerd gedurende ten minste vier maanden na vaccinatie⁴⁴ en na intramusculaire injectie door het hele lichaam wordt verspreid.⁴⁵Voor de vaccins tegen het coronavirus van het severe acute respiratory syndrome 2 (SARS-CoV-2) is gekozen voor het spike-eiwit, mogelijk omdat het celingang mogelijk maakt. Dit eiwit is echter niet inert, maar is veeleer de oorzaak van veel van de pathologie die gepaard gaat met ernstig COVID-19, waaronder endotheliale schade,⁴⁶ coagulation abnormalities⁴⁷ en longschade.

Het is leerzaam op te merken dat de WHO vóór de invoering van de mRNA-producten een prioriteitenlijst heeft goedgekeurd van potentiële ernstige ongewenste voorvallen van bijzonder belang die zich kunnen voordoen als rechtstreeks gevolg van COVID-19-vaccins.

De lijst was gebaseerd op het specifieke vaccinplatform, bijwerkingen van eerdere vaccins in het algemeen, theoretische associaties op basis van diermodellen en COVID-19specifieke immunopathogenese⁴⁰ (zie figuur 2).

Doet het vaccin meer kwaad dan goed?

De meest objectieve manier om te bepalen of de voordelen van de vaccins opwegen tegen de nadelen is de analyse van de effecten op de “sterfte door alle oorzaken”. Dit omzeilt de netelige kwestie van wat als een COVID-19-dood moet worden aangemerkt, en houdt ook volledig rekening met eventuele negatieve effecten van het vaccin. Het zou op zijn minst verrassend zijn indien tijdens een schijnbaar dodelijke pandemie niet duidelijk en ondubbelzinnig zou kunnen worden aangetoond dat een doeltreffend vaccin de sterfte door alle oorzaken vermindert.

Het cruciale mRNA-onderzoek van Pfizer bij volwassenen toonde geen statistisch significante vermindering van de sterfte door alle oorzaken, en in absolute cijfers waren er zelfs iets meer sterfgevallen in de behandelingsarm dan in de placebogroep.

Werk van Fenton et al. toonde een ongewone piek in de sterfte in elke leeftijdsgroep van de niet-gevaccineerde bevolking, die samenvalt met de uitrol van het vaccin voor elke leeftijdsgroep.⁴⁸ De snelle afname van de omvang van deze populatie betekent dat een klein tijdsverschil dit effect theoretisch kunstmatig zou kunnen veroorzaken. Een alternatieve verklaring is de (meer waarschijnlijke) mogelijkheid dat een stijging van de sterfte na vaccinatie ten onrechte werd toegeschreven aan de niet-gevaccineerde bevolking: met andere woorden, degenen die werden geteld als “niet-gevaccineerde sterfgevallen” zouden in feite degenen zijn die binnen 14 dagen na de vaccinatie waren overleden (een verzoek om vrijheid van informatie [FOI] heeft nu bevestigd dat de autoriteiten in Zweden sterfgevallen binnen 14 dagen na de vaccinatie inderdaad categoriseerden als niet-gevaccineerd, waardoor een misleidend beeld ontstond van werkzaamheid versus sterfte).

Het is mogelijk dat de overmatige hartstilstand en de aanhoudende druk op ziekenhuizen in 2021/2022 door niet-COVID-19 opnames allemaal wijzen op een niet-COVID-19 gezondheidscrisis die wordt verergerd door interventies, waaronder natuurlijk ook lockdowns en/of vaccins.

Gezien deze waarnemingen en de herbeoordeling van de gegevens van gerandomiseerde gecontroleerde proeven met mRNA-producten, lijkt het moeilijk te beweren dat de invoering van vaccins in alle leeftijdsgroepen netto gunstig is geweest. Men kan weliswaar stellen dat de vaccins enkele levens hebben gered bij ouderen of anderszins kwetsbare groepen, maar dat lijkt in het beste geval twijfelachtig voor andere delen van de bevolking, en wanneer de mogelijke schade op korte, middellange en onbekende langere termijn in aanmerking wordt genomen (met name voor meervoudige injecties, waarvoor gewoon geen degelijke veiligheidsgegevens bestaan), lijkt de invoering bij de hele bevolking in het beste geval een roekeloze gok. Het is belangrijk te erkennen dat het risico van bijwerkingen van het vaccin constant blijft, terwijl de voordelen mettertijd afnemen, aangezien nieuwe varianten (1) minder virulent zijn en (2) niet gericht zijn op een verouderd product. Na beoordeling van de gegevens blijft het een reële mogelijkheid dat de plotselinge hartdood van mijn vader verband hield met het vaccin. Een pauze en heroverweging van het vaccinatiebeleid voor COVID-19 had al veel eerder plaats moeten vinden.

Again the link to the original english article, including the text of this article, also as a Dutch version.

Voor Deel 2 van het paper, klik je hier