Trends in Excess Deaths

Debate between Andrew Bridgen and Danny Kruger

Friday 20th October 2023 Commons Chamber

[Andrew Bridgen]

I thank the hon. Gentleman for his intervention. He is absolutely right: the media have let the British public down badly. There will be a full press pack going out to all media outlets following my speech, with all the evidence to back up all the claims I will make, but I do not doubt that there will be no mention of it in the mainstream media.

One might think that a debate about excess deaths would be full of numbers, but this speech does not contain many numbers, because most of the important numbers are being kept hidden. Other data has been oddly presented in a distorted way, and concerned people seeking to highlight important findings and ask questions have found themselves inexplicably under attack.

Before debating excess deaths, it is important to understand how excess deaths are determined. To understand whether there is an excess, by definition, we need to estimate how many deaths would have been expected. The Organisation for Economic Co-operation and Development uses 2015 to 2019 as a baseline, and the Government’s Office for Health Improvement and Disparities uses a 2015 to 2019 baseline, modelled to allow for ageing. I have used that data here. Unforgivably, the Office for National Statistics has included deaths in 2021 as part of its baseline calculation for expected deaths, as if there was anything normal about the deaths in 2021. By exaggerating the number of deaths expected, the number of excess deaths can be minimised. Why would the ONS want to do that?

There is just too much that we do not know, and it is not good enough. The ONS publishes promptly each week the number of deaths registered. While that is commendable, it is not the data point that really matters. There is a total failure to collect, never mind publish, data on deaths that are referred for investigation to the coroner. Why does that matter? A referral means that it can be many months—or, given the backlog, many years—before a death is formally registered. Needing to investigate the cause of a death is fair enough, but failing to record when the death happened is not.

Because of that problem, we have no idea how many people died in 2021, even now. The problem is greatest for the younger age groups, where a higher proportion of deaths are investigated. This data failure is unacceptable and must change. There is nothing in a coroner’s report that can bring anyone back from the dead, and those deaths should be reported. The youngest age groups are important not only because they should have their whole lives ahead of them. If there is a new cause of excess mortality across the board, it would not be noticed so much in the older cohorts, because the extra deaths would be drowned out among the expected deaths. However, in the youngest cohorts, that is not the case.

There were nearly two extra deaths a day in the second half of 2021 among 15 to 19-year-old males, but potentially even more if those referred to the coroner were fully included. In a judicial review of the decision to vaccinate yet younger children, the ONS refused in court to give anonymised details about those deaths. It admitted that the data it was withholding was statistically significant. It said:

“the ONS recognises that more work could be undertaken to examine the mortality rates of young people in 2021, and intends to do so once more reliable data are available.”

How many more extra deaths in 15 to 19-year-olds will it take to trigger such work? Surely the ONS should be desperately keen to investigate deaths in young men. Why else do we have an independent body charged with examining mortality data? Surely the ONS has a responsibility to collect data from coroners to produce timely information.

Let us move on to old people. Most deaths in the old are registered promptly, and we have a better feel for how many older people are dying. Deaths from dementia and Alzheimer’s show what we ought to expect: there was a period of high mortality coinciding with covid and lockdowns, but ever since, there have been fewer deaths than expected. After a period of high mortality, we expect and historically have seen a period of low mortality, because those who have sadly died cannot die again.

Those whose deaths were slightly premature because of covid and lockdowns died earlier than they otherwise would have. That principle should hold true for every cause of death and every age group, but that is not what we are seeing. Even for the over-85-year-olds, according to the Office for Health Improvement and Disparities, there were 8,000 excess deaths—4% above the expected levels—for the 12 months starting in July 2020. That includes all of the autumn 2020 wave of covid when we had tiering and the second lockdown and all of the first covid winter. However, for the year starting July 2022, there were more than 18,000 excess deaths in this age group—9% above expected levels. That is more than twice as many in a period when there should have been a deficit and when deaths from diseases previously associated with old age were fewer than expected. I have raised my concerns about NG163 and the use of midazolam and morphine, which may have caused—and may still be causing—premature deaths in the vulnerable, but that is, sadly, a debate for another day.

There were just over 14,000 excess deaths in the under 65-year-olds before vaccination from April 2020 to the end of March 2021. However, since that time, there have been more than 21,000 excess deaths, ignoring the registration delay problem, and the majority of those deaths—58% of them—were not attributed to covid. We turned society upside down before vaccination for fear of excess deaths from covid, but today we have substantially more excess deaths, and in younger people, and there is a complete eerie silence. The evidence is unequivocal. There was a clear stepwise increase in mortality following the vaccine roll-out. There was a reprieve in the winter of 2021-22 because there were fewer than expected respiratory deaths, but otherwise the excess has been incessantly at this high level.

Ambulance data for England provides another clue. Ambulance calls for life- threatening emergencies were running at a steady 2,000 calls a day until the vaccine roll-out. From then, they rose to 2,500 daily, and calls have stayed at that level since. The surveillance systems designed to spot a safety problem have all flashed red, but no one is looking. Claims for personal independence payments from people who have developed a disability and cannot work rocketed with the vaccine roll-out and have continued to rise ever since. The same was seen in the US, which also started with the vaccine roll-out, not with covid. A study to determine the vaccination status of a sample of such claimants would be relatively quick and inexpensive to perform, yet nobody seems interested in ascertaining this vital information. Officials have chosen to turn a blind eye to this disturbing, irrefutable and frightening data, much like Nelson did—and for far less honourable reasons. He would be ashamed of us.

Furthermore, data that has been used to sing the praises of the vaccine is deeply flawed. Only one covid-related death was prevented in each of the initial major trials that led to authorisation of the vaccines, and that is taking the data entirely at face value, whereas a growing number of inconsistencies and anomalies suggest that we ought not to do this. Extrapolating from that means that between 15,000 and 20,000 people had to be injected to prevent a single death from covid. To prevent a single covid hospitalisation, more than 1,500 people needed to be injected. The trial data showed that one in 800 injected people had a serious, adverse event, meaning that they were hospitalised or had a life-threatening or life-changing condition. The risk of this was twice as high as the chance of preventing a covid hospitalisation. We are harming one in 800 people to supposedly save one in 20,000. That is madness.

The strongest claims have too often been based on modelling carried out on the basis of flawed assumptions. Where observational studies have been carried out, researchers will correct for age and comorbidities to make the vaccines look better. However, they never correct for socioeconomic or ethnic differences as that would make vaccines look worse. That matters. For example, claims of higher mortality in less vaccinated regions of the United States took no account of the fact that this was the case before the vaccines were rolled out. That is why studies that claim to show that the vaccines prevented covid deaths also showed a marked effect of them preventing non-covid deaths. The prevention of non-covid deaths was always a statistical illusion and claims of preventing covid deaths should not be assumed when that illusion has not been corrected for. When it is corrected for, the claims of efficacy for the vaccines vanish with it.

Covid disproportionately killed people from ethnic minorities and lower socioeconomic groups during the pandemic. In 2020, deaths among the most deprived were up by 23% compared with 17% for the least deprived. However, since 2022 the pattern has reversed, with 5% excess mortality among the most deprived compared with 7% among the least deprived. These deaths are being caused by something different.

In 2020, the excess was highest in the oldest cohorts, and there were fewer than expected deaths among younger age groups. However, since 2022, the 50 to 64-year-old cohort has had the highest excess mortality. Even the youngest age groups are now seeing a substantial excess, with a 9% excess in the under-50s since 2022 compared with 5% in the over-75 group.

Despite London being a younger region, the excess in London is only 3%, whereas it is higher in every more heavily vaccinated region of the UK. It should be noted that London is famously the least vaccinated region in the UK by some margin. Studies comparing regions on a larger scale show the same thing. Studies from the Netherlands, Germany and the whole world each show that the highest mortality after vaccination was seen in the most heavily vaccinated regions.

So we need to ask: what are people dying of? Since 2022, there has been an 11% excess in ischemic heart disease deaths and a 16% excess in heart failure deaths. In the meantime, cancer deaths are only 1% above expected levels, which is further evidence that this is not simply some other factor that affects deaths across the board, such as failing to account for an ageing population or a failing NHS. In fact, the excess itself has a seasonality, with a peak in the winter months. The fact that it returns to baseline levels in summer is a further indication that this is not due to some statistical error or an ageing population alone.

Dr Clare Craig from HART—the Health Advisory & Recovery Team—first highlighted a stepwise increase in cardiac arrest calls after the vaccine roll-out in May 2021. HART has repeatedly raised concerns about the increase in cardiac deaths, and it has every reason to be concerned. Four participants in the vaccine group of the Pfizer trial died from cardiac arrest compared with only one in the placebo group. Overall, there were 21 deaths in the vaccine group up to March 2021, compared with 17 in the placebo group. There are serious anomalies about the reporting of deaths in this trial, with the deaths in the vaccine group taking much longer to report than those in the placebo group. That is highly suggestive of a significant bias in what was supposed to be a blinded trial.

An Israeli study clearly showed that an increase in cardiac hospital attendances among 18 to 39-year-olds correlated with vaccination, not with covid. There have now been several post-mortem studies demonstrating a causal link between vaccination and coronary artery disease leading to death up to four months after the last dose. We need to remember that the safety trial was cut short to only two months, so there is no evidence of any vaccine safety beyond that point. The decision to unblind the trials after two months and vaccinate the placebo group is nothing less than a public health scandal. Everyone involved failed in their duty to the truth, but no one cares.

The one place that can help us understand exactly what has caused this is Australia, which had almost no covid when vaccines were first introduced, making it the perfect control group. The state of South Australia had only 1,000 cases of covid across its whole population by December 2021, before omicron arrived. What was the impact of vaccination there? For 15 to 44-year-olds, there were historically 1,300 emergency cardiac presentations a month. With the vaccine roll-out to the under-50s, this rocketed to over 2,172 cases in November 2021 in this age group alone, which was 67% more than usual. Overall, 17,900 South Australians had a cardiac emergency in 2021 compared with only 13,250 in 2018, which is a 35% increase. The vaccine must clearly be the No. 1 suspect for this, and it cannot be dismissed as a coincidence. Australian mortality overall has increased from early 2021, and that increase is due to cardiac deaths.

These excess deaths are not due to an ageing population, because there are fewer deaths from the diseases of old age. These deaths are not an effect of covid, because they have happened in places that covid had not reached. They are not due to low statin prescriptions or undertreated hypertension, as Chris Whitty would suggest, because prescriptions did not change, and any effect would have taken many years and been very small. The prime suspect must be something that was introduced to the population as a whole, something novel. The prime hypothesis must be the experimental covid-19 vaccines.

The ONS published a dataset of deaths by vaccinated and unvaccinated. At first glance, it appears to show that the vaccines are safe and effective. However, there were several huge problems with how it presented that data. One was that for the first three-week period after injection, the ONS claimed that there were only a tiny number of deaths—the number the ONS would normally predict to occur in a single week. Where were the deaths from the usual causes? When that was raised, the ONS claimed that the sickest people did not get vaccinated and therefore the people who were vaccinated were self-selecting for those least likely to die. Not only was that not the case in the real world, with even hospices heavily vaccinating their residents, but the ONS’s own data show that the proportion of sickest people was equal in the vaccinated and the unvaccinated groups. That inevitably raises serious questions about the ONS’s data presentation. There were so many problems with the methodology used by the ONS that the statistics regulator agreed that the ONS data could not be used to assess vaccine efficacy or safety. That tells us something about the ONS.

Consequently, HART asked the UK Health Security Agency to provide the data it had on people who had died and therefore needed to be removed from its vaccination dataset. That request has been repeatedly refused, with excuses given including the false claim that anonymising the data would be the equivalent of creating it even though there is case law that anonymisation is not considered the creation of new data. I believe that if this data was released, it would be damning.

Some claim that so many lives have been saved by mass vaccination that any amount of harm, suffering and death caused by the vaccines is a price worth paying. They are delusional. The claim of 20 million lives saved is based on now discredited models which assume that covid waves do not peak without intervention. There have been numerous waves globally now that demonstrate that is not the case. It was also based on there having been more than half a million lives saved in the UK. That is more than the worst-case scenario predicted at the beginning of the pandemic. For the claim to have been true, the rate at which covid killed people would have had to take off dramatically at the beginning of 2021 in the absence of vaccination. That is ludicrous and it bears no relation to the truth.

In the real world, Australia, New Zealand and South Korea had a mortality rate of 400 deaths per million up to summer 2022 after they were first hit with omicron. How does that compare? With the Wuhan strain, France and Europe as a whole had a mortality rate of under 400 deaths per million up to summer 2020. Australia, New Zealand and South Korea were all heavily vaccinated before infection, so tell me: where was the benefit? The UK had just over 800 deaths per million up to summer 2020, so twice as much, but we know omicron is half as deadly as the Wuhan variant. The death rates per million are the same before and after vaccination, so where were the benefits of vaccination?

The regulators have failed in their duty to protect the public. They allowed these novel products to skip crucial safety testing by letting them be described as vaccines. They failed to insist on safety testing being done in the years since the first temporary emergency authorisation. Even now, no one can tell us how much spike protein is produced on vaccination and for how long—yet another example of where there is no data for me to share with the House.

When it comes to properly recording deaths due to vaccination, the system is broken. Not a single doctor registered a death from a rare brain clot before doctors in Scandinavia forced the issue and the Medicines and Healthcare products Regulatory Agency acknowledged the problem. Only then did these deaths start to be certified by doctors in the UK. It turns out the doctors were waiting for permission from the regulator and the regulator was waiting to be alerted by the doctors. This is a lethal circularity. Furthermore, coroners have written regulation 28 reports highlighting deaths from vaccination to prevent further deaths, yet the MHRA said in response to a freedom of information request that it had not received any of them. The systems we have in place are clearly not functioning to protect the public.

The regulators also missed the fact that in the Pfizer trial, the vaccine was made for the trial participants in a highly controlled environment, in stark contrast to the manufacturing process used for the public roll-out, which was based on a completely different technology. Just over 200 participants were given the same product that was given to the public, but not only was the data from these people never compared to those in the trial for efficacy and safety but the MHRA has admitted that it dropped the requirement to provide the data. That means that there was never a trial on the Pfizer product that was actually rolled out to the public, and that product has never been compared with the product that was actually trialled.

The vaccine mass production processes use vats of Escherichia coli and present a risk of contamination with DNA from the bacteria, as well as bacterial cell walls, which can cause dangerous reactions. This is not theoretical; this is now sound evidence that has been replicated by several labs across the world. The mRNA vaccines were contaminated by DNA, which far exceeded the usual permissible levels. Given that this DNA is enclosed in a lipid nanoparticle delivery system, it is arguable that even the permissible levels would have been far too high. These lipid nanoparticles are known to enter every organ of the body. As well as this potentially causing some of the acute adverse reactions that have been seen, there is a serious risk of this foreign bacterial DNA inserting itself into human DNA. Will anybody investigate? No, they won’t.

[Danny Kruger (Devizes) (Con)]

I am grateful to the hon. Gentleman for giving way; I am conscious that time is tight. I recognise that he is making a very powerful case. Does he agree that the Government should be looking at this properly and should commission a review into the excess deaths, partly so that we can reassure our constituents that the case he is making is not in fact valid and that the vaccines are not the cause behind these excess deaths?

[Andrew Bridgen]

I thank the hon. Gentleman for his support on this topic. Of course that is exactly what any responsible Government should do. I wrote to the Prime Minister on 7 August 2023 with all the evidence of this, but sadly I am still awaiting a response.

What will it take to stop these products? Their complete failure to stop infections was not enough; we all know plenty of vaccinated people who have caught and spread covid. The mutation of the virus to a weaker variant—omicron—was not enough, the increasing evidence of the serious harms to those of us who were vaccinated was not enough, and now the cardiac deaths and the deaths of young people are apparently not enough either.

It is high time that these experimental vaccines were suspended and a full investigation into the harms that they have caused was initiated. History will be a harsh judge if we do not start using evidence-based medicine. We need to return to basic science and basic ethics immediately, which means listening to all voices and investigating all concerns.

In conclusion, the experimental covid-19 vaccines are not safe and are not effective. Despite there being only limited interest in the Chamber from colleagues—I am very grateful to those who have attended—we can see from the Public Gallery that there is considerable public interest. I implore all Members of the House, those who are present and those who are not, to support calls for a three-hour debate on this important issue. Mr Deputy Speaker, this might be the first debate on excess deaths in our Parliament—indeed, it might be the first debate on excess deaths in the world—but, very sadly, I promise you it will not be the last.

Vaccines: Potential Harms

Debate between Andrew Bridgen and Danny Kruger

Tuesday 13th December 2022 Commons Chamber

[Andrew Bridgen]

The hon. Gentleman is absolutely right. Those who feel that they have been damaged by the vaccine should of course have the full support of their elected Members of Parliament and the NHS. Only a couple of weeks ago, I was interviewed by a journalist from a major news outlet who said that he was being bombarded by calls from people who said that they were vaccine-harmed but unable to get the support they wanted from the NHS. He also said that he thought this would be the biggest scandal in medical history in this country. Disturbingly, he also said that he feared that if he were to mention that in the newsroom in which he worked, he would lose his job. We need to break this conspiracy of silence.

It is instructive to note that, according to pharmaco-vigilance analysis, the serious adverse effects reported by the public are thought to represent only 10% of the true rate of serious adverse events occurring within the population. The gold standard of understanding the benefit and harm of any drug is the randomised controlled trial. It was the randomised controlled trial conducted by Pfizer that led to UK and international regulators approving the BioNTech-Pfizer mRNA vaccine for administration in the first place.

Contrary to popular belief, that original trial of approximately 40,000 participants did not show any statistically significant reduction in death as a result of vaccination, but it did show a 95% relative risk reduction in the development of infection against the ancestral, more lethal strain of the virus. However, the absolute risk reduction for an individual was only 0.84%. In other words, from its own data, Pfizer revealed that we needed to vaccinate 119 people to prevent one infection. The World Health Organisation and the Academy of Medical Royal Colleges have previously stated and made it clear that it is an ethical responsibility that medical information is communicated to patients in absolute benefit and absolute risk terms, which is to protect the public from unnecessary anxiety and manipulation.

Very quickly, through mutations of the original strain—indeed, within a few months—covid fortunately became far less lethal. It quickly became apparent that there was no protection against infection at all from the vaccine, and we were left with the hope that perhaps these vaccines would protect us from serious illness and death. So what does the most reliable data tell us about the best-case scenario of individual benefit from the vaccine against dying from covid-19? Real-world data from the UK during the three-month wave of omicron at the beginning of this year reveals that we would need to vaccinate 7,300 people over the age of 80 to prevent one death. The number needed to be vaccinated to prevent a death in any younger age group was absolutely enormous.

[Danny Kruger (Devizes) (Con)]

I am very grateful to my hon. Friend for bringing this debate to the House. It is a very important debate that we should be having. He is talking about the relative risks for different cohorts of the population. He will remember that, when the vaccine was first announced, the intention was that it would be used only for those who were vulnerable and the elderly because, as he says, the expectation was that the benefit to younger people was minor. Does he agree that it would be helpful for the Minister to explain to us why the original advice that the vaccines would be rolled out only for the older population, and would not be used for children in particular, was laid aside and we ended up with the roll-out for the entire population, including children?

--- Later in debate ---

[Andrew Bridgen]

I thank my hon. Friend for that intervention. Clearly this is related to all mRNA vaccinations. He will be well aware that many of us have had the AstraZeneca vaccine, which has effectively been withdrawn because of health concerns. Indeed, I will declare to the House that I am double-vaccinated with AstraZeneca, which has now been withdrawn.

Ministers may understandably wish to defer the responsibility for a decision such as withdrawing vaccines from the population to regulators such as the Medicines and Healthcare products Regulatory Agency, or in America the Food and Drug Administration. Historically, when undertaking the approval of any drug, the regulators ultimately end up relying on the summary results from the drug companies in their sponsored trials, where the raw data is kept commercially confidential. Furthermore, the MHRA has a huge financial conflict of interest, receiving 86% of its funding from the pharmaceutical industry it is supposed to regulate. In effect, we have the poacher paying the gamekeeper.

In a recent investigation by The BMJ into the financial conflicts of interest of the drug regulators, the sociologist Donald Light said:

“It’s the opposite of having a trustworthy organisation independently and rigorously assessing medicines. They’re not rigorous, they’re not independent, they are selective, and they withhold data.”

He went on to say that doctors and patients

“must appreciate how deeply and extensively drug regulators can’t be trusted so long as they are captured by industry funding.”

Similarly, another investigation revealed that members of the Joint Committee on Vaccination and Immunisation had huge financial links to the Bill and Melinda Gates Foundation running into billions of pounds. Ministers, the media and the public know that the foundation is heavily invested in pharmaceutical industry stocks.

Unfortunately, the catastrophic mistake over the approval, and the coercion associated with this emergency-use authorisation medical intervention, are not an anomaly, and in many ways this could have been predicted by the structural failures that allowed it to occur in the first place. Those shortcomings are rooted in the increasingly unchecked visible and invisible power of multinational corporations—in this case, big pharma. We can start by acknowledging that the drug industry has a fiduciary obligation to produce profit for its shareholders, but it has no fiduciary obligation to provide the right medicines for patients.

The real scandal is that those with a responsibility to patients and with scientific integrity—namely, doctors, academic institutions and medical journals—collude with the industry for financial gain. Big pharma exerts its power by capturing the political environment through lobbying and the knowledge environment through funding university research and influencing medical education, preference shaping through capture of the media, financing think-tanks and so on. In other words, the public relations machinery of big pharma excels in subterfuge and engages in smearing and de-platforming those who call out its manipulations. No doubt it will be very busy this evening.

It is no surprise, when there is so much control by an entity that has been described as “psychopathic” for its profit-making conduct, that one analysis suggests that third most common cause of death globally after heart disease and cancer is the side effects of prescribed medications, which were mostly avoidable. Because of those systemic failures, doctors often receive biased information, deliberately manipulated by the pharmaceutical industry, which exaggerates the benefits and the safety of their drugs. Furthermore, the former editor of The BMJ, Richard Smith, claims that research misconduct is rife and is not effectively being tackled in the UK institutions, stating:

“Something is rotten in…British medicine and has been for a long time”.

It has also been brought to my attention by a whistleblower from a very reliable source that one of these institutions is covering up clear data that reveals that the mRNA vaccine increases inflammation of the heart arteries. It is covering this up for fear that it may lose funding from the pharmaceutical industry. The lead of that cardiology research department has a prominent leadership role with the British Heart Foundation, and I am disappointed to say that he has sent out non-disclosure agreements to his research team to ensure that this important data never sees the light of day. That is an absolute disgrace. Systemic failure in an over-medicated population also contributes to huge waste of British taxpayers’ money and increasing strain on the NHS.

[Danny Kruger]

My hon. Friend is being very good with his time. I just want to call his attention to some research, since I chair the all-party parliamentary group for prescribed drug dependence. He refers to the waste of money; there is £500 million being spent every year by the NHS on prescribed drugs for people who should not be on those habit-forming pills, causing enormous human misery as well as waste for the taxpayer.

[Andrew Bridgen]

I thank my hon. Friend for making a point that only reinforces the items in my speech that the public need to know. I thank him again for his support.

We need an inquiry into the influence of big pharma on medications and our NHS. That is been called for many occasions and by some very influential people, including prominent physicians such as the former president of the Royal College of Physicians and personal doctor to our late Queen, Sir Richard Thompson. On separate occasions in the last few years those calls have been supported and covered in the Daily Mail, The Guardian and, most recently, The i newspaper.

We are fighting not just for principles of ethical, evidence-based medical practices, but for our democracy. The future health of the British public depends on us tackling head-on the cause of this problem and finding meaningful solutions. In 2015 a commentary by Richard Houghton, editor-in-chief of The Lancet, suggested that possibly half of the published medical literature “may simply be untrue”. He wrote that

“science has taken a turn toward darkness”,

and asked who is going to take the first step to clean up the system.

That first step could start this evening with this debate. It starts here, with the vaccine Minister and the Government ensuring in the first instance an immediate and complete suspension of any more covid vaccines with their use of mRNA technology. Silence on this issue is more contagious than the virus itself, and now so should courage be. I would implore all the scientists, medics, nurses and those in the media who know the truth about the harm these vaccines are causing to our people to speak out.

We have already sacrificed far too many of our citizens on the altar of ignorance and unfettered corporate greed. Last week the MHRA authorised those experimental vaccines for use in children as young as six months. In a Westminster Hall debate some weeks ago, I quoted a report by the Journal of the American Medical Association studying the effect of the covid-19 mRNA vaccination on children under five years of age. It showed that one in 200 had an adverse event that resulted in hospitalisation, and symptoms that lasted longer than 90 days.

As the data clearly shows to anyone who wants to look at it, the mRNA vaccines are not safe, not effective and not necessary. I implore the Government to halt their use immediately. As I have demonstrated and as the data clearly shows, the Government’s current policy on the mRNA vaccines is on the wrong side of medical ethics, it is on the wrong side of scientific data, and ultimately it will be on the wrong side of history.

Covid-19 Vaccines: Safety

Debate between Andrew Bridgen and Danny Kruger

Monday 24th October 2022 Westminster Hall

[Danny Kruger (Devizes) (Con)]

It is a pleasure to serve under your chairmanship, Sir Roger.

I am grateful to my hon. Friend the Member for Carshalton and Wallington (Elliot Colburn), who gave a very good defence of the vaccine programme and of the Medicines and Healthcare products Regulatory Agency. I respect that, but I regret his response to my hon. Friend the Member for Christchurch (Sir Christopher Chope), who raised the point about medical expertise that casts some doubt on the vaccines. My hon. Friend the Member for Carshalton and Wallington chose to smear all opponents of the vaccine programme. Of course there are lunatics out there who make absurd and outrageous claims, but there are many reasonable and respectable people who have anxieties about the vaccine programme, particularly people who have suffered as a result of the programme and their families.

I am a member of the all-party parliamentary group on covid-19 vaccine damage, which my hon. Friend the Member for Christchurch chairs. The APPG looks at vaccine injuries, and we had what I think was our first meeting last week in a Committee room in Portcullis House. I am afraid there were only a tiny handful of colleagues there, but well over a hundred members of the public attended, which is not the usual story for an APPG. I felt somewhat ashamed, on behalf of Parliament, that that was the first time that those members of the public—including families of the bereaved, who are themselves injured citizens—had had the opportunity to be in a room with members of this House, but I am very pleased that we are having this debate, and particularly pleased that there is an opportunity for members of the public to hear from the Minister on this topic.

I should say to members of the public who are watching that we have in Westminster Hall today a very good Minister, the Under-Secretary of State for Health and Social Care, my hon. Friend the Member for Sleaford and North Hykeham (Dr Johnson), who is genuinely committed to health, including public health, and she showed a real interest in this topic and in the effect of covid policies when she was a Back-Bench MP.

Although many questions about our covid response need to be answered, the UK is by no means the worst offender. We are not Canada, New Zealand or China—places where Governments think they can exterminate covid by depriving their population of the most basic civil liberties. However, I am afraid that we still have many questions to ask ourselves, and even much to be ashamed of. I put on record that in hindsight I am particularly ashamed of my vote to dismiss care workers who did not want to receive the vaccine. I very much hope that the 40,000 care workers who lost their jobs can be reinstated, and indeed compensated. A group of us—including, I think, the Minister—held out against compulsory vaccination of health workers when that was proposed by the Government last winter. I think that resistance turned the tide, to a degree, on Government policy, and we emerged from the lockdowns more quickly than we might otherwise have done, yet we still have a policy of mass vaccination, which I want to query on behalf of constituents who have written to me about it.

My query starts with a simple point. In October 2020, when preparations were being made for the vaccine roll-out, Kate Bingham, the head of the vaccines agency, said:

“There’s going to be no vaccination of people under 18. It’s an adult-only vaccine, for people over 50, focusing on health workers and care home workers and the vulnerable.”

Why was vaccination extended to the whole population? I do not think we have ever had a completely satisfactory answer to that question. I ask it again, because my concern is that extending the vaccination programme became an operation in public persuasion—an operation in which dissent was unhelpful or even immoral, and an operation that justified the suppression and even vilification of those who raised concerns.

[Andrew Bridgen (North West Leicestershire) (Con)]

I thank my hon. Friend for giving way. Unlike any other vaccine, the covid vaccine was given to people who had natural immunity because they had provably contracted the virus. Why were those people vaccinated?