Covid mNRA debate in Parliament.

Andrew Bridgen and Sir Christopher Chope.

Andrew Bridgen:

"I beg to move,

That this House has considered the covid-19 pandemic response and trends in excess deaths; and calls on the covid-19 inquiry to move onto its module 4 investigation into vaccines and therapeutics as soon as possible.

We are witnesses to the greatest medical scandal in this country in living memory, and possibly ever: the excess deaths in 2022 and 2023. Its causes are complex, but the novel and untested medical treatment described as a covid vaccine is a large part of the problem. I have been called an anti-vaxxer, as if I have rejected those vaccines based on some ideology. I want to state clearly and unequivocally that I have not: in fact, I am double vaccinated and vaccine-harmed. Intelligent people must be able to tell when people are neither pro-vax nor anti-vax, but are against a product that does not work and causes enormous harm to a percentage of the people who take it.

I am proud to be one of the few Members of Parliament with a science degree. It is a great shame that there are not more Members with a science background in this place; maybe if there were, there would be less reliance on Whips Office briefings and more independent research, and perhaps less group-think. I say to the House in all seriousness that this debate and others like it are going to be pored over by future generations, who will be genuinely agog that the evidence has been ignored for so long, that genuine concerns were disregarded, and that those raising them were gaslit, smeared and vilified.

One does not need any science training at all to be horrified by officials deliberately hiding key data in this scandal, which is exactly what is going on. The Office for National Statistics used to release weekly data on deaths per 100,000 in vaccinated and unvaccinated populations—it no longer does so, and no one will explain why. The public have a right to that data. There have been calls from serious experts, whose requests I have amplified repeatedly in this House, for what is called record-level data to be anonymised and disclosed for analysis. That would allow meaningful analysis of deaths after vaccination, and settle once and for all the issue of whether those experimental treatments are responsible for the increase in excess deaths.

Far more extensive and detailed data has already been released to the pharma companies from publicly funded bodies. Jenny Harries, head of the UK Health Security Agency, said that this anonymised, aggregate death by vaccination status data is “commercially sensitive” and should not be published. The public are being denied that data, which is unacceptable; yet again, data is hidden with impunity, just like in the Post Office scandal. Professor Harries has also endorsed a recent massive change to the calculation of the baseline population level used by the ONS to calculate excess deaths. It is now incredibly complex and opaque, and by sheer coincidence, it appears to show a massive excess of deaths in 2020 and 2021 and minimal excess deaths in 2023. Under the Toggle showing location ofColumn 505old calculation method, tried and tested for decades, the excess death rate in 2023 was an astonishing 5%—long after the pandemic was over, at a time when we would expect a deficit in deaths because so many people had sadly died in previous years. Some 20,000 premature deaths in 2023 alone are now being airbrushed away through the new normal baseline.

Shocking things happened during the pandemic response. In March 2020, the Government conducted a consultation exercise on whether people over a certain age or with certain disabilities should have “do not resuscitate” orders, known as DNRs, imposed upon them. A document summarising the proposals was circulated to doctors and hospitals; it was mistakenly treated as formal policy by a number of care homes and GPs up and down the country, who enacted it. At the same time, multiple hospitals introduced a policy that they would not admit patients with DNRs, because they thought that they would be overwhelmed. The result was that people died who did not need to die while nurses performed TikTok dances.

The average time to death from experiencing covid symptoms and testing positive was 18 days. It is a little-known fact that the body clears all the viruses within around seven days; what actually kills people is that some, especially the vulnerable, have an excessive immune response. Doctors have been treating that response for decades with steroids, antibiotics for secondary pneumonia infections and other standard protocols, but they did not do so this time. Even though the virus was long gone, doctors abandoned the standard clinical protocols because covid was a “new virus”—which it was not. They sent people home, told them to take paracetamol until their lips turned blue, and then when those people returned to hospital, they sedated them, put them on ventilators and watched them die.

The protocol for covid-19 treatment was a binary choice between two treatment tracks. Once admitted, ill patients were either ventilated in intensive care or—if they were not fit for that level of care—given end of life medication, including midazolam and morphine. The body responsible for that protocol, NG163, which was published on 3 April 2020, is called the National Institute for Health and Care Excellence, or NICE. Giving midazolam and morphine to people dying of cancer is reasonable, but there is a side effect, which is that those drugs have a respiratory depressant effect. It is hard to imagine a more stupid thing to do than giving a respiratory suppressant to someone who is already struggling to breathe with the symptoms of covid-19, but that is exactly what we did.

Can the Minister explain why midazolam was removed from the same updated guideline NG191—the antecedent of NG163—on 30 November 2023? As it was removed, is it now considered and admitted that it was a mistake to ignore the warnings of so many experts about including that specific drug, midazolam, in NG163 when it was introduced? It has been confirmed in letters from Ministers to families whose loss of loved ones was down to this protocol that Ministers are now saying that doctors and nurses should have treated the individual patient with their own knowledge, rather than strictly following NICE guideline NG163. If legal cases for unlawful killing are brought, can the Minister tell us who is going to be taking the blame? Will it be NICE, will it be NHS England or will the individual doctors and nurses be held to account?Toggle showing location ofColumn 506

Interestingly, NICE has now removed these alternative protocols, including NG163, from its website, although every other historical protocol is still there for reference. Could the Minister tell us why NICE has removed this protocol from its website? Is it ashamed of the harm it has caused? It certainly should be. What can we learn from this? We learn that very few doctors dare challenge what they are told. Protocols with no authors are distributed, and doctors fall into line.

There is a huge, stark contrast in how deaths and illnesses after vaccination have been recorded compared with those after covid. After a positive covid test, any illness and any death was attributed to the virus. After the experimental emergency vaccine was administered, no subsequent illness and no death was ever attributed to the vaccine. Those are both completely unscientific approaches, and that is why we have to look at other sources of data—excess deaths—to determine whether there is an issue.

First, however, I want to address the phrase “safe and effective”. The fear deliberately stoked up by the Government promoted the idea of being rescued by a saviour vaccine. The chanting of the “safe and effective” narrative began, and the phrase seemed to hypnotise the whole nation. “Safe and effective” was the sale slogan of thalidomide. After that scandal, rules were put in place to prevent such marketing in future by pharma companies, and they are prohibited from using “safe and effective” without significant caveats.

That did not matter this time because, with covid-19 vaccines, the media, the Government and other authorities turned into big pharma’s marketing department, and it is very hard now to hear the word “safe” without the echo of the words “and effective”, but they are not safe and effective. In March 2021, when the majority of UK citizens had already received these novel products, Pfizer signed a contract with Brazil and South Africa saying that

“the long-term effects and efficacy of the Vaccine are not currently known and…adverse effects of the Vaccine...are not currently known.”

That is verbatim from the Pfizer contracts.

These so-called vaccines were the least effective vaccines ever. Is there anyone left under any illusion that they prevented any infections? When he was at the Dispatch Box for Prime Minister’s questions on 31 January, even the Prime Minister, in answer to my question, could not bring himself to add “and effective” to his “safe” mantra. In his own words, he was “unequivocal” that the vaccines are “safe”. The word “safe” means without risk of death or injury. Why is the Prime Minister gaslighting the 163 successful claims made to the vaccine damage payment scheme, totalling £19.5 million in compensation for harm caused by the covid vaccines? Have these people not suffered enough already? Those 163 victims are the tip of the iceberg, by the way. It also should be noted that the maximum payment is only £120,000, so each of those 163 victims got the maximum possible award, which should tell us something. The same compensation scheme paid out a total of only £3.5 million between 1997 and 2005, with an average of only eight claims per year, and that is for all claims for the entire country for all vaccines administered. So much for “safe”.

How about effective? On 25 October 2021, the then Prime Minister—the right hon. Member for Uxbridge and South Ruislip, Boris Johnson—even admitted that the vaccineToggle showing location ofColumn 507

“doesn’t protect you against catching the disease and it doesn’t protect you against passing it on.”

Looking at the levels of the virus found in sewage shows that the post-vaccine wave was of the same order of magnitude and duration as the previous waves. This proves that the vaccines changed nothing. They were not safe, and they were not effective.

Those who imposed these vaccines knew full well that they could never prevent infection from a disease of this kind. An injection in the arm cannot do that. Only immunity on the surface of the airways and the lungs can prevent viral infection; antibodies in the blood cannot. In Dr Anthony Fauci’s words,

“it is not surprising that none of the predominantly mucosal respiratory viruses have ever been effectively controlled by vaccines.”

He continued:

“This observation raises a question of fundamental importance: if natural mucosal respiratory virus infections do not elicit complete and long-term protective immunity against reinfection, how can we expect vaccines, especially systemically administered non-replicating vaccines, to do so?”

They knew that the so-called vaccines would never protect from infection, which explains why they never tested for protection from infection.

Only a few days ago, the Association of the British Pharmaceutical Industry rapped Pfizer on the knuckles for the sixth time, and said that its marketing practices had brought the industry into disrepute. It was asked to pay a paltry £30,000 in administrative expenses, with no fine on top. The person heading the ABPI at the moment is also the head of Pfizer UK. The Medicines and Healthcare products Regulatory Agency has a statutory duty to carry out this work, and it has handed its responsibility to the industry. This is an outrageous conflict of interest.

Let us turn back to excess deaths. The Australian Government have launched an inquiry into Australia’s excess deaths problem. Australia is almost unique as a case study for excess deaths; as it had the vaccine before it had covid, its excess deaths are not so easily blamed on the long-term side effects of a virus. Like us, it saw a rise in deaths, which began in May 2021 and has not let up since. The impact was evident on the ambulance service first. South Australia saw a 67% increase in cardiac presentations of 15 to 44-year-olds. That increase peaked in November 2021, before covid hit. We saw a similar, deeply worrying effect here. In the UK, calls for life-threatening emergencies rose from 2,000 per day to 2,500 per day in May 2021, and that number has never returned to normal.

By October 2021, despite it being springtime in Australia, headlines reported that ambulances were unable to drop off patients in hospitals, which were already at full capacity. Mark McGowan, Premier of Western Australia, said that he could not explain the overwhelmed hospitals:

“Our hospitals are under enormous pressure. This has been something no one has ever seen before. Why it is, is hard to know.”

In April 2022, Yvette D’Ath, Queensland’s Health Minister, said about the most urgent ambulance calls, called “code ones”:

“I don’t think anyone can explain why we saw a 40% jump in code ones... We just had a lot of heart attacks and chest pains and trouble breathing, respiratory issues. Sometimes you can’t explain why those things happen but unfortunately, they do.”Toggle showing location ofColumn 508

I think we could explain this if we were to look at the link to the vaccine roll-out. Omicron did cause some excess deaths in Australia from 2022 onwards. However, there was a huge chunk of excess deaths prior to that, which doctors have not been able to blame on the virus. Could those deaths be caused by the vaccine? Very few people dare even ask that question.

It is important to remember how the vaccines were made. Traditionally, the key to making a vaccine is to ensure that the pathological, harmful parts of the virus or bacteria are inactivated, so that the recipient can develop an immune response without danger of developing the disease. In stark contrast, the so-called covid vaccines used the most pathological or harmful part of the virus—the spike protein—in its entirety. The harm is systemic because, contrary to what everyone was told, the lipid nanoparticles, encapsulating the genetic material, spread through the whole body after injection, potentially affecting all organs. At the time, everyone was being reassured that the injection was broken down in the arm at the injection site. Regulators ought to have known that those were problems.

Furthermore, it is now plentifully evident that the drug results in continued spike protein production for many months—even years, in some people. The deaths thus far have been predominantly cardiac, but there may unfortunately be many more deaths to come from these novel treatments, which may induce extra cancer deaths. Dr Robert Tindle is the retired director of the Clinical Medical Virology Centre in Brisbane, and emeritus professor of immunology. This month he published a paper highlighting the multiple potential harms from the vaccines, including harm to the immune system. As anyone who knows anything about biology will know, anything that disrupts the immune system can potentially increase the risk of cancer.

There are other reasons to be concerned about cancer being induced by these vaccines. Cancer is a genetic disease disorder that arises from errors in DNA, allowing cells to grow uncontrollably. Moderna has multiple patents describing methods for reducing the risk of cancer induction from its mRNA products. That risk comes from the material interrupting the patient’s DNA. It turns out that an mRNA injection has very high quantities of DNA in it, and that massively increases the risk of disturbing a patient’s own DNA. Worse still, the DNA that was injected contained sequences that were hidden from the regulator. That is the SV40, or simian virus 40 promoter region, which has been linked to cancer and has been found in the Pfizer vaccines. That was no accident. Yet again, crucial information was hidden from the regulator and the public with absolute impunity. An independent study in Japan, published last week, has found links between increased cancer rates in Japan and those who took the first and subsequent booster vaccines. Perhaps that explains why Pfizer acquired a cancer treatment company for a reported $43 billion earlier this year.

In conclusion, the evidence is clear: these vaccines have caused deaths. Despite that, they have been described as safe and effective. However, for a proportion of people who took them, the vaccines have caused serious harm and death, and they will have raised the risk of cancer for many more. Nor are they effective. The vaccine does not prevent infection or transmission, and when the data is looked at objectively, it shows that the vaccine does not prevent serious illness or death. Those are hard Toggle showing location ofColumn 509truths to face, but we must face them if we want to learn the lessons of the last few years. At some point we will have to face up to all the evidence that is building. It was fairly convincing 18 months ago when I first spoke out, but it is unequivocal now.

It is time to take the politics out of our science, and to put actual science back into our politics. I ask the House to support the motion today, and for Baroness Hallett’s inquiry to open module 4 on the safety and efficacy of the experimental covid-19 vaccines. Given the evidence, I call on the Government once again to immediately suspend the use of all mRNA treatments in both humans and animals, pending the outcome of that inquiry."

Sir Christopher Chope:

"As we have just witnessed, feelings are very strong on this issue, and large numbers of people have suffered directly or indirectly as a result of having covid-19 vaccines. For most people—the vast majority—the covid-19 vaccines were very good news, and they made an enormous contribution to the public health of the country, but that does not mean that we should turn a blind eye to those for whom the vaccines were bad news. In the earlier debate today, I reiterated my request that the Government take effective action, through the vaccine damage payment scheme, to ensure that those people for whom the vaccines were bad news receive proper compensation.

As the hon. Member for North West Leicestershire (Andrew Bridgen) reminded us, the maximum payment under that scheme is £120,000. That figure has not been updated in line with inflation since 2007; had it been updated, it would now be about £200,000. Why do the Government not update it? Relatively small numbers of people are involved, but it seems as though there is reluctance on the Government’s part to face up to the reality that, for a small proportion of people, the vaccines were bad news.

When we had this debate initially, soon after the roll- out of the vaccines, the Government were unequivocal in saying that the vaccines were safe and effective, and with no qualification at all. Subsequently, AstraZeneca issued essentially a warning notice to practitioners, which said that they should be cautious about the roll-out of some of the vaccines to some patients. People who wish to make claims against the vaccine manufacturers and/or the Government—civil claims to supplement the £120,000 that they have already been awarded—are finding it difficult to get access to lawyers to pursue their claims, particularly if those claims arise from vaccines administered after AstraZeneca issued its first warning against the safety of its vaccines in certain circumstances.

A large number of people across the country look to the Government to intervene, first, to ensure that the vaccine damage payment scheme is updated, and secondly, to ensure that the people who applied under that scheme have their claims dealt with in a reasonable timeframe. Many of those claims are not. There are more than 9,000 claims, and 4,000-plus have not even been resolved yet. The delays extend to 18 months or more. The consequence for many claimants is that they are unable Toggle showing location ofColumn 510to begin their civil action, but a civil action has to be brought within three years of the cause of action arising if it is not to be affected by the limitation period.

I have asked the Prime Minister—I had a meeting with him, and have raised this at Prime Minister’s questions —whether the Government will intervene to ensure that the three-year limitation period does not apply to people still waiting for a determination of their claim under the vaccine damage payment scheme, if they wish to go on and sue the Government or the manufacturers. It is a matter of simple equity and justice. I have yet to have a substantive answer from the Government. I am due to meet the Secretary of State for Health and Social Care next week, and I hope that by then she will be able to assure me—she is a lawyer, as well as a Secretary of State—that nobody will be denied justice as a result of the Government’s delays in administering the vaccine damage payment scheme.

I very much share the disappointment of the hon. Member for North West Leicestershire, who introduced this debate, that module 4 of the public inquiry has been postponed. Last August, there was a preliminary hearing, and there was some potent advocacy by the lawyers representing the victim groups who wanted to give evidence in module 4. That evidence will be extremely compelling when it is heard by the inquiry. It was a big disappointment to those groups, to me and to others that module 4 was postponed. We have been told that it has been postponed until January next year. The reasons for that seem rather weak and feeble, but the inquiry is independent. Evidence that was to have been given in July will now not be heard until January next year. The implications are serious for those seeking compensation for their suffering, but it is also significant for that other group of people.

That is because module 4 deals not just with vaccines but with therapeutics. There is a big issue about therapeutics, because Evusheld, the therapeutic that was meant to be available in particular for those who were immuno- suppressed and not able to take the vaccines, was never approved by NICE. A second version of Evusheld was being brought forward, but that has also still not been approved.

My constituent Bernard Mathysse has written to me in recent months to draw my attention to a letter sent on 26 March to the Prime Minister by a group of charities concerned with the issue. It calls for the Government to intervene and ensure that an early decision is made on what can be done to help immunocompromised people who cannot access the vaccines in any event. My constituent says that

“France has given emergency authorisation to Evusheld 2, and has got it into patients within a month of authorisation”.

He believes that other European countries will do the same. The United States has given Pemgarda—another drug—emergency authorisation, and so on.

Why can we not get a commitment from the Government to ensure that Evusheld is available to clinically vulnerable people? My constituent also wrote to me in July 2023 expressing the need to fast-track an essential pre-exposure prophylaxis drug. The consequence for him is that he and his wife have been in effect shielding for about four years: they meet friends only outside, they do not travel on public transport or go by aeroplane, they ask the family to test before a visit, they mask indoors, and they have to assess every situation to gauge the risks involved. Toggle showing location ofColumn 511That obviously means that they have a much restricted and isolated life, to their detriment, but that could be resolved if the Evusheld issue was taken seriously by the Government. If module 4 had been heard this summer, perhaps Baroness Hallett, as an interim recommendation, could have said, “The Government must get on with that.”

Mr Philip Hollobone:

"I am hugely enjoying my hon. Friend’s speech. I, too, have a constituent who is immunosuppressed and, unbelievably, still shielding, which is putting huge pressure on the family. Does not the slowness of the decision over this therapeutic stand in sorry contrast with the rapid decision taken on vaccines in the first place?"

Sir Christopher Chope

"Exactly. One of the inhibitions there may have been on the Government’s part was that, to justify the use of emergency vaccines, it was necessary for them to believe that there was no alternative. Of course, if those alternative measures had been recognised as a suitable way of providing some protection to individuals against covid-19, that would have undermined the vaccine manufacturers’ case that they needed emergency authorisation for their vaccines without going through the normal testing procedures.

The continuing slowness of the Government in responding to requests for licensing of Evusheld reinforce the feeling out there among many people that something funny is going on here and that, if we had come forward with those therapeutic measures at the beginning, many lives would have been saved, such an extensive vaccination programme would not have been needed, and the Government would have saved a lot of money. There is an issue there, but that is why the part of the motion that regrets the postponement of that element of the covid-19 inquiry is important.

We can debate academically or in political circles the issue of the excess deaths, but it is interesting that the Government concede that there have been excess deaths. The House of Commons Library’s briefing produced on 15 April for this debate says:

“The government has acknowledged an increase in the number of excess deaths in England and Wales and has attributed these to a combination of factors, such as the prevalence of heart disease, flu and heart disease.”

The emphasis is on heart disease, but many people feel that the increase in heart conditions and disease has been exacerbated by the very vaccines that people were persuaded to take to protect them against covid-19. According to an article last year, Dr Thomas Levy said that, on his estimate,

“vaccines are causing heart injury in at least 2.8% of people who receive the covid injections.”

He estimated that

“a minimum of 7 million Americans now have hearts damaged by covid ‘vaccines.’ And although there’s no way of being certain at this time, he said, it’s within the realm of possibility that over 100 million people in America have some degree of heart damage from the injections—not myocarditis but heart damage that will be detectable with a troponin test.”

There may be a link between the propensity of vaccines to damage people’s hearts and what the House of Commons Library, interpreting the Government figures, concedes is an issue of excess deaths attributable to heart disease."

Wera Hobhouse:

"The hon. Gentleman makes a good point that there is not a single medical intervention that does not also have risks—the medical profession will always acknowledge that—but is it not about a balance of the benefits against the risks? Ultimately, the judgment was made by those who supported the covid vaccine that the benefits far outweighed the risks imposed by the vaccine."