
PART 3

DR CLARE CRAIG
Today we are publishing Dr Clare Craig’s presentation delivered at the People’s Vaccine Inquiry press conference last week. Full details and videos of the event and additional presentations can be found here.
The first presentation, published on Monday, by Dr Jonathan Engler, explained why the People’s Inquiry was so necessary in view of Lady Hallett’s disgraceful refusal to honestly address the extent and cause of vaccine injury. The second, by Dr Elizabeth Evans, published yesterday, focused on Hallett’s total disregard for the abandonment of medical ethics accompanying the vaccines’ authorisation and roll-out.
Dr Clare Craig, a consultant diagnostic pathologist, who has carried out significant research into the covid epidemic as an individual, was the third speaker. She reiterated that the press conference is not about what was said at the inquiry. It is about what was not said, she said, not forgotten or overlooked; not missed, but deliberately excluded. She went on:
THE LEAD counsel, Hugo Keith, repeatedly interrupted anyone wishing to put forward narrative-challenging evidence. He made the predetermined position crystal clear before a word of evidence had been heard. He said: ‘The exercise of pronouncing the last word on the efficacy and safety of specific vaccines may prove to serve little purpose.’
Little purpose? To whom? These questions matter immensely – to the silenced, to the injured and to the bereaved. But instead of scrutiny, we got slogans. Instead of evidence, we heard echoes of certainty. Not a debate – it was doctrine. They worshipped the novel covid vaccines.
Shamefully, and without evidence, Hugo Keith talked about ‘entirely effective’ vaccines which were ‘undoubted successes’ with ‘lifesaving benefits . . . which . . . vastly outweighed the very rare risk of a serious side effect.’ Adding ‘without any doubt’, he even went as far as saying they offered ‘the promised land’.
Would he say that about other novel pharmaceutical products?
Other participants repeatedly claimed the vaccines were ‘undoubtedly’ beneficial, ‘an extraordinary achievement’, ‘world-beating’ and ‘saved millions of lives’.
Where was the evidence? Buried beneath a mountain of faith. This new faith was built on fantasy born of modelling and a statistical illusion.
I am a scientist. It is, in theory, possible to train the immune system to recognise pathogens. It must be possible to subscribe to that scientific fact but challenge when a particular example manifestly fails. A failed medicine is not a medicine. It is a cash machine.
The models created an illusion of benefit
- The models assumed a never-ending tsunami of infection and death without lockdowns and vaccines – numerous subsequent waves have disproved that.
- The models assumed vaccines prevented 90 per cent of deaths – so, of course, they ‘proved’ millions of lives were saved.
- The models ignored Omicron, which killed fewer people. Omicron stayed in the upper airway like a normal coronavirus. Omicron was half as deadly in the unvaccinated. Omicron the inquiry barely acknowledged.
No one dared admit that Omicron was less severe from the start.
The only mention of Omicron’s severity in oral evidence was from
Sajid Javid who farcically got the evidence – as a former Health Secretary, no less – completely wrong, saying, ‘We knew Omicron was a lot more severe’.
Now we come to thestatistical ‘cheap trick’(a phrase coined by Martin Neil and Norman Fenton to describe a phenomenon many of us have been trying to bring to public attention for years. The illusion of benefit):
- Only around 10 per cent of people are susceptible to each wave.
- The vaccine suppressed immunity for two weeks, triggering infections earlier in those susceptible.
- The two-week window after vaccination? They called it ‘unvaccinated’. A barefaced lie
- That made the vaccinated look safer –
- And the unvaccinated look doomed.
- A rigged game. A statistical illusion.
- Thereafter the unvaccinated continued to be affected but the vaccinated wave had finished early.
- When the next wave arrived – weeks or months later – they called this waning. It wasn’t waning. It was the washing out of a statistical illusion.
One tragic example was Peter Rossiter. He was 39. A pianist. A son. A life ahead of him. Four days after his second dose, he fell ill with covid. This is the danger period. The immune system is hammered by the vaccine in this period so people become more susceptible to infection.
His mother said at the Inquiry, ‘his white blood count was almost zero . . . he very sadly fell very seriously ill very quickly’.
Pfizer said:’He wasn’t fully protected.’They knew the two-week period was risky. But instead of admitting it they used these cases to prop up the illusion of benefit. Shameful.
In the real world it was clear in 2021 that the vaccines did not reduce infections. Afterwards, there was a pivot to claim they prevented severe disease and death. Different witnesses at Hallett still clung to different parts of this false narrative.
Chris Whitty was asked about vaccine mandates and clung to the fantasy that vaccine mandates could alter transmission by reducing infection, calling it ‘blindingly obvious’.
Drug safety expert Professor Prieto-Alhambra said: ‘They lost their ability to prevent transmission, we believe, because of this inability to prevent infection in the first place’.But he still kept up the illusion. He returned to the Imperial College model which is based on the original claims of a tsunami of cases and deaths, and claimed they had shown’that the vaccines saved over 14million lives globally’ and that they ‘helped to prevent long covid’. Claims based on such modelling are worthless and unscientific.
Meanwhile some witnesses were still leaning heavily on the claim that it protected from severe illness and deaths. Dame Kate Bingham, head of the Vaccine Taskforce, said they were ‘very effective at controlling serious disease and death but they don’t block transmission. They’re not durable. They’re expensive’.
Lord James Bethell, who signed the authorisations, said: ‘The vaccination programme had delivered, for most of the population, a really good protection, certainly from severe disease and death. It didn’t stop transmission, it didn’t stop long covid, it didn’t work for absolutely everyone.’
Matt Hancock repeated the trope that covid ‘after a vaccine . . . tended to be much milder’.
And they kept parroting the 14million-lives-saved myth. A number plucked straight from models but untouched by real-world evidence.
There were contradictions on death prevention. Professor Wei Lim, JCVI [Joint Committee on Vaccination and Immunisation] chair, claimed: ’99 per cent of covid mortality is in Phase 1 groups’ – those targeted for the very earliest jabs. Yet the UKHSA insisted only 14,000 deaths were prevented by June 2021. Then, somehow, over the summer time, by September they magically saved 109,000 more.
Reality says otherwise.
- UK, Portugal and Ireland were outliers, but the USA and the rest of Europe saw no benefit from vaccines in 2021.
- Deaths kept coming in line with virus in the sewage and people developing antibodies.
And the clinical trials? The authorisations were all based on only a single claimed placebo covid death in the trial evidence. This is science by cowboys. Millions are being spent on the lawyers for this inquiry who let this pass without challenge.
Representatives from AZ, Pfizer and Moderna were all questioned. Dr Justin Green from AZ claimed that on the basis of only one death in the placebo group.
He said ‘that gave us a really good indication that we had an excellent product here that was going to be really effective’. Even the US trial safety board condemned the ‘misleading’ press releases that quoted 100 per cent effectiveness against death on the back of this one death. Yet no one at the inquiry dared to question him. Dr Green went on to opine about how ‘amazing’ it would have been to have real world data collection systems in the future ‘that also had really deep and rich safety data’.
The Moderna rep, Mr Darius Hughes, was asked: ‘So no suspected unexpected serious adverse reactions during the trials?’ He concurred. On oath. Whereas the head of the Commission on Human Medicines, Professor Munir Pirmohamed, said there had been a facial paralysis signal from Bell’s Palsy (which can be lifelong), from ‘the beginning’.
Other mentions of clinical trials were forbidden.
When Ruth O’Rafferty of the Scottish Vaccine Injured group brought up the critically important differences between the trial product in the lab and the mass-produced product in the vats, Hugo Keith interrupted her saying, ‘I’m so sorry, I’m going to have to interrupt you there, we don’t have the time or the wherewithal to be able to go into some of these areas in this sort of detail.’
When Charlet Crichton of UKCV Family mentioned participants being vaccine injured in the trials and their data being scrubbed from the reports he said, ‘All right, I’m going stop you there . . . We can’t be looking at individual cases.’That was a rule that did not apply to those with a covid label. Nor did Charlet in fact mention an individual case. She was talking about fundamental corruption in the only reliable measure we have of vaccine safety, and the counsel to the Inquiry simply did not want to know. Nor did the Chair intervene to find out more.
When Ruth O’Rafferty brought up regulatory failures outlined in a 2005 parliamentary report, the recommendations of which have not been implemented, he said ‘All right. We’re in danger of veering off.’
There were other banned topics.
- Lipid nanoparticle risks? Not discussed.
- Cardiac risks and sudden death? Ignored.
- How much spike is produced, in which organs and for how long? Off-limits.
- Different doses of Pfizer vs Moderna? Not explored.
- Morphine and midazolam, antibiotics, vitamin D, budesonide? Not relevant.
But the word rare? That was everywhere.
Hugo Keith said: ‘I must emphasise the rarity, more often the extreme rarity, of the serious adverse effects that were suffered.’And he really did emphasise it. They said the word ‘rare’ 134 times: ‘rare, very rare or extremely rare’ – repeated again and again.
Yet excess deaths, working-age disabilities and heart disease soared after spring 2021. This was true everywhere – including Singapore and Australia which had had minimal covid but were vaccinated at scale along with everyone else.
- In the trial the risk of an important serious adverse event was 1 in 800 risk for mRNA vaccines and 1 in 550 for Pfizer.
- There is evidence that the Pfizer mass-produced vaccine had two to at least 13 times the reported adverse reactions of the lab version used in the trial.
- 3 per cent of mRNA recipients have evidence of heart damage.
That is not rare.
This was no inquiry – this was idolatry. They worshipped the vaccine narrative. They silenced the blasphemers. They cast out the apostates. Even five years later, questioning these myths is heresy.
The twin pillars of the covid era are:
- The myth of an unstoppable tsunami of death.
- The myth that vaccines saved us.
Both are false.
The benefits were an illusion. The harms were real. And those who dared to speak out have been attacked.
History will not look kindly on those who refused to listen.
This article (Inside the People’s Vaccine Inquiry – Part Three) was created and published by Conservative Woman and is republished here under “Fair Use” with attribution to the author Dr Clare Craig
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Inside the People’s Vaccine Inquiry – Part 4
DR ROS JONES
All this week we have been publishing the key papers presented at The People’s Vaccine Inquiry press conference on Tuesday of last week. On Monday Dr Jonathan Engler explained its purpose in view of Lady Hallett’s disgraceful refusal to honestly address the extent and cause of vaccine injury. On Tuesday Dr Elizabeth Evans shone her torch on Hallett’s total disregard for medical ethics accompanying the vaccines’ authorisation and roll-out. The third paper, delivered by consultant pathologist Dr Clare Craig, focused not on what was said at the Hallett Inquiry about vaccine ‘safety and efficacy’ but on what was not said. Today retired paediatrician Dr Ros Jones reports on the indefensible folly of the covid vaccine roll-out for children that Hallett has also failed to address.
I’M ROS Jones, a retired consultant paediatrician, and I am here on behalf of over 200 experienced health professionals and academics. We’ve sent numerous letters to the regulators and politicians about the folly of covid vaccines for children, most reported by TCW.* We, like others here, were asked for a detailed witness statement which we provided, even agreeing to it being shared with one of their ‘experts’. When we were told we wouldn’t be called, we were nevertheless thanked and told our statements had been very useful to the Inquiry team in their deliberations.
However, nothing we provided was used at all. We were simply ascribed to the ‘misinformation brigade’. A propos of which, our first fully referenced letter with all our names was sent by Chris Whitty’s department to the Counter Disinformation Unit, who previously monitored online child pornography & terrorism! [Ed’s note: In fact a press release published on March 30 2020 announced that the Government was cracking down on ‘spread of false coronavirus information online’, that specialist units ‘are operating to combat misinformation about coronavirus’ and that ‘five to ten incidents are being identified and tackled each day‘.]
Following on from Dr Evans [the previous speaker], firstly the ethics:
It was very clear that whatever bug was doing the rounds in spring 2020, it did not affect children to any significant degree, yet the government measures caused disproportionate harm. It wasn’t just the school closures, it was the testing and masking and the ‘don’t kill your granny’ messaging. And parents saw first-hand the harms of lockdowns. So when the vaccines were presented as the only route back to normal, parents were not immune from the messaging.
The risk/benefit balance is widely variable by age so a one-size-fits-all was never right. Matt Hancock was absolutely clear this was an adult vaccine; Kate Bingham, chair of the Vaccine Taskforce, went further to say it was for over-50s with comorbidities. Professor Lim, the Chair of the Joint Committee on Vaccination and Immunisation (JCVI) in his evidence confirmed that the phase 1 roll-out was expected to cover 99 per cent of the mortality from Covid-19. Yet none questioned why the vaccine juggernaut seemed to be unstoppable.
So that brings me to the approval process. MHRA authorised the use of Pfizer for 12-15s on the basis of 1131 vaccinated children followed for two months. You don’t need to be a medic to know that is not a measure of safety. Yet Kate Bingham said the studies were large! The Medicines Health products and Regulatory Authority (MHRA) only checked data provided by Pfizer. They then passed the baton to the JCVI.
The Moral and Ethical Advisory Group (MEAG), a multifaith and ethics group set up in 2019, asked specifically to be involved in discussions re children’s vaccine but their planned meeting in June was cancelled as they were told there were no plans to vaccinate kids. In fairness, JCVI meeting minutes show they were worried – they were looking at myocarditis reports from Israel and the US. And they said NO, not for healthy under-18s. But 48 hours later they held an emergency meetingat the request of Chris Whitty, the Chief Medical Officer (CMO) to ‘reconsider their decision’. Why was Chris Whitty not questioned about this? Or about the CMO’s decision that this would help keep children in school and hence be good for mental health? He admitted their calculations (it worked out at 15 mins per child) allowed no time out of class for the vaccination procedure, let alone for any adverse effects.
Turning to myocarditis, this has been acknowledged and added to the patient information leafet, but their so-called expert misquoted the Oxford study, saying it showed more myocarditis with covid than with the vaccine (as stated in the conclusion sentence of their abstract) but even the results section of the abstract actually reported that for males under 40, myocarditis wassix timesmore likelyafter vaccination than after infection. Again the MHRA were never pinned down as to why they didn’t give more detail of rates by age to enable informed consent.
Everyone just kept repeating ‘VERY rare’ and ‘recovers quickly’. How rare depends on how hard you look. Israel, where the first cases were reported, sent letters to all their paediatricians, cardiologists and emergency physicians, telling them what to look out for and this resulted in ~ 1 in 6,000, so not ‘very rare’, Mr Keith, that is ‘rare’.
But Thailand did what the MHRA should have demanded of Pfizer: they organised a prospective study in two large secondary schools with cardiac blood tests and ECG before and 1/52 after vaccination and they found a worrying 1 in 29 with either clinical or subclinical myo- or pericarditis. That is ‘common’.
As for ‘recovers quickly’, teenagers admitted to US hospitals with chest pain seemed to recover quickly but 89 per cent had abnormal cMRIs. JCVI wanted to see their follow-up data before making a decision. If they had been allowed to delay, they would have learned that 60 per cent were still abnormal 6/12 later. These are abnormalities which have been associated with reduced five-year survival in viral myocarditis. These kids need their hearts for another 70 years!
Sajid Javid said Boris Johnson kept badgering him not to let Britain lag behind Spain and Israel, but instead of saying ‘PM, there’s a process that must be followed,’ he should have been saying, ‘Well, Prime Minister, it’s about a serious safety concern – I am sure you wouldn’t want to see children dying in your attempt to stay ahead in this race.’
Lastly, something else Mr Javid said was that he felt ‘if you get a vaccine, it should be for a positive reason: to want to protect your health or protect your loved ones from infection, rather than some kind of inducement.’Maybe he was unaware of the Charlton Athletic football tickets for the first 1,000 at their pop-up vacc hub. Moderna have been guilty of bringing the pharmaceutical Industry into disrepute for allowing a £1,500 offer to children participating in a trial of their new booster. To return to the legality of children only allowed to receive treatments for their own personal health benefit, who authorised these NHS advertisements?

I despair!
*A list of those letters and campaigns which Dr Jones led or was central to published at the time on TCW:
Why Johnson must halt this dangerous child vaccine programme
Sixty doctors plead with chief medical officers to reject child vaccination
Our constellation of concerns over vaccine for children
Deafening silence of health watchdogs over danger of child jabs
Why are watchdogs still deaf to the danger of child jabs?
Post-vaccine myocarditis is not ‘mild’, warn doctors
Health professionals: Join our child vaccine plea to the new PM
This article (Inside the People’s Vaccine Inquiry – Part Four) was created and published by Conservative Woman and is republished here under “Fair Use” with attribution to the author Dr. Ros Jones
*****
The Covid Inquiry Calling the Vaccines “Safe and Effective” is Like the Post Office Inquiry Calling Horizon “Reliable”

BEN KINGSLEY AND MOLLY KINGSLEY
Module Four of the Covid Inquiry has just ended. Its brief and highly-curated existence has confirmed for us all that not only is the inquiry studiously avoiding any confrontation with the most contentious issues of the Covid period, it also appears knowingly to be facilitating the creation of a false record of some core aspects of that period.
It has been conspicuous for some time that the inquiry is determined to swerve topics such as the harm versus benefit equation for lockdowns; the integrity of the vaccine trials; the net benefit, safety and efficacy of the Covid vaccines; the ethics of vaccinating children for the benefit of adults; the role of censorship, propaganda and coercion; and relatedly, the manifest absence of informed consent in the Covid vaccination programme.
All of these critical topics have either been sidestepped or ruled beyond the scope of the inquiry. More corrosively, though, in a number of ways the inquiry appears to be allowing and at times even encouraging the creation of a false record.
Rubber-stamping rather than interrogating complex topics
There are some issues which, although technically within scope for the inquiry, have been given only a superficial airing with no meaningful scrutiny.
Two striking examples concern the role of ethics in decision-making and the Government’s decision to roll out the Covid vaccine to children.
The topics of ethics and ethical frameworks have been referenced only briefly and in passing throughout the inquiry to date, but the questions posed in Module Four conspicuously have failed even to scratch the surface of the many serious ethical violations involved in the vaccine rollout process, including coercive policies, the frustration of informed consent and medicating children to mitigate a policy decision (not a medical decision) to close schools.
Indeed, across all four modules to date, the inquiry has failed to ask a single question about the fact that official meeting records of the Government’s expert ethics advisory committee (MEAG) show that its criticisms of key policies, including in summer 2021 when plans to vaccinate healthy children against Covid came to a head, were suppressed or ignored before the committee was abruptly demobilised.
Likewise, the highly unorthodox and unprecedented decision of the Chief Medical Officers in September 2021 to approve the mass vaccination of children over the heads of the JCVI has been mentioned only so that it could be rubber-stamped by the inquiry as necessary and uncontroversial. The Inquiry would have us believe that there is nothing to see, no questions to be asked of these highly consequential events. That is manifestly not the case.
Establishing flawed presumptions
The inquiry has itself created – and has allowed witnesses to buttress – flawed evidential presumptions that in some cases go to the very heart of the issues that ought to be investigated if meaningful lessons are to be learned. For example, at the outset of Module Four, Hugo Keith KC anchored all of his subsequent interrogations with a series of highly-contested or outright fallacious assertions, including these (emphasis added):
“The overall process by which the MHRA ensured that… all of the vaccines authorised [by it for temporary emergency use]… were effective and acceptably safe, was no different in substance to the process that would have applied had those applications been made… for full marketing authorisations.”
“The absolutely clear expert opinion of the [single expert] instructed by the inquiry… is that the vaccines, those three COVID-19 vaccines, were entirely effective.”
“My Lady, empirically, it is beyond argument that vaccinated people were far less likely to get COVID-19 with symptoms.”
“I must emphasise the rarity, more often the extreme rarity, of the serious adverse effects that were suffered, and the fact that the figures demonstrate beyond any doubt that the life-saving benefits of the UK COVID-19 vaccines vastly outweighed the very rare risk of a serious side-effect.”
Though the inquiry had declared at the outset that it was not competent to address questions of the safety or risk-benefit of the Covid vaccines, instead of not taking a position on these important and contentious topics, the inquiry has presumed, or allowed to be presumed, answers which only support the official narrative — such as that the Covid vaccines were entirely effective.
This matters greatly because, self-evidently, conclusions reached on the basis of a false or unreliable presumption are themselves unreliable and quite possibly false.
It would be as if the Post Office Inquiry had started its process by stating a presumption that the Horizon system was entirely reliable, and that any errors could only have been the result of extremely rare glitches: clearly, such an assumption would have undermined the entirety of the inquiry’s subsequent interrogation of the evidence.
Failing to contemplate uncomfortable realities
There are areas in which the inquiry has been undeniably one-sided or partisan in its outlook. This has been very evident in its consideration of the effects of mis- and dis-information on the vaccination programme.
The inquiry has anchored its analysis with a presumption that it was only commentary challenging official public health messages or critical of the Government’s policy decisions that was capable of being mis- or dis-information. It has not even contemplated the uncomfortable possibility that mis- and dis-information might have originated with vaccine manufacturers, public health officials or the Government.
This alarming myopia — whether negligent or intentional — is all the more striking when one considers that, since 2020, there have been a staggering 16 adverse regulatory judgments (at least) against the main UK Covid vaccine manufacturers in relation to their vaccine products, with the industry regulator, the PMCPA, publishing a litany of damning findings including that manufacturers have:
- propagated misleading information and made unsubstantiated claims about the safety of their Covid vaccines;
- published misleading information about the efficacy of those vaccines;
- promoted unlicensed uses of those vaccines; and
- paid unlawful financial inducements to promote their vaccines.
Leaving false or misleading evidence unchallenged
The inquiry has, we believe, also allowed witnesses knowingly or recklessly to record false evidence. This is a serious allegation, but one which appears to be supported by the transcripts. To give just two examples:
Hugo Keith KC asked a series of leading questions to Professor Lim Wei Shen KBE, the Acting Chair of the JCVI during the Covid period, on the topic of the JCVI’s controversial decision to not recommend vaccination for 12 to 15 year olds in September 2021.
Hugo Keith: And so in that risk-benefit analysis, as you said earlier, between the marginal benefits of vaccination against the very rare but not to be ignored risk of myocarditis, was it a more difficult balance to draw?
Witness: It was a very difficult balance, a hugely fine balance, quite unlike the balance of an older person who might have an adverse effect from vaccination.
Hugo Keith: Do you also consider in the balance, health inequalities, Long Covid, the impact on mental health of children and young persons of being vaccinated or not being vaccinated, as well as the ethics?
Witness: Correct. We consider all those things.
Those leading questions elicited a definitive confirmation that the JCVI considered, among other things, the ethics of extending the vaccination programme to children. This appears flatly to contradict official records both of the JCVI’s meetings to discuss the vaccination of 12 to 15 year olds (which are extensive but contain not one mention of ethics) and of an earlier JCVI meeting (held on May 7th 2020) which had discussed the role of MEAG and ethics, and recorded that:
The Committee agreed that JCVI advice would be based on scientific principles from the available scientific evidence and this would not include detailed ethical considerations which were for DHSC to consider, informed by MEAG.
And on the same topic of the Covid vaccine’s rollout to children, when explaining the CMOs decision to proceed with the rollout, Sir Chris Whitty had earlier misdescribed the JCVI’s advice as characterising the risks of vaccinating children aged 12 to 15 as being “even smaller” than the marginal benefits at an individual child level.
What the JCVI in fact had said — and it seems highly improbable that both Chris Whitty and the inquiry’s lawyers had not read that advice in preparing for his evidence session — was that “the [JCVI] is of the opinion that the benefits from vaccination are marginally greater than the potential known harms but acknowledges that there is considerable uncertainty regarding the magnitude of the potential harms” (emphasis added).
In each of these situations a witness has been allowed by the inquiry to carelessly or knowingly give flawed or false evidence to the inquiry in relation to a critical safeguarding matter of significant public interest. These are but two examples of a growing list that we are compiling.
Prohibiting inconvenient questions – and answers
At many times throughout its hearings to date, including during Module Four, the inquiry has tightly controlled the proceedings and appears to have prohibited inconvenient questions from being asked, or answers given.
It was conspicuous, for example, that when AstraZeneca was called to give oral evidence, not one of the core participants had been given time to ask questions — are we to believe that none had any questions?
Two stark examples of the latter, both concerning topics of significant relevance for the inquiry, occurred in relation to the topics of lockdown harms and benefits and censorship.
When in Module Two Rishi Sunak MP, at the time Prime Minister, broached the subject of a QALY (quality adjusted life years) analysis of the first lockdown and commented that the lockdown “in its severity and duration was likely to have generated costs that are greater than the likely benefit”, he was immediately closed down by Hugo Keith KC, who replied that “we’re not interested in QALYs”.
Similarly, when Michael Gove MP in the same module attempted to raise the question of the lab leak theory, saying “there is a significant body of judgement that believes that the virus itself was man-made”, he was promptly cut off by Hugo Keith KC who intervened, bluntly: “It forms no part of the terms of reference of this inquiry to address that somewhat divisive issue, so we’re not going to go there.”
Conclusions
Module Four has perhaps more than any other module so far revealed the flaws which permeate this inquiry and which will compromise almost any finding it may ultimately make.
Imagine a Post Office Inquiry in which, in addition to assuming at the outset that the Horizon IT system had been infallible, the Chair ruled as off-limits any questioning of the reliability of that IT system; in which anyone who had historically questioned the reliability of the system, or the motivations of Post Office executives and prosecutors, was presumed to be an irredeemable spreader of disinformation; in which examples of false evidence were allowed to become embedded as a matter of public record; and in which lawyers for the sub-postmasters were not permitted an opportunity to pose questions to Fujitsu executives.
Yet this bizarrely Kafkaesque image reflects the reality of the Covid Inquiry. Not only can we not hope to learn lessons of any value from a public inquiry so lacking in curiosity and critical thinking, and so beset by fanatical adherence to a pre-conceived story of the UK’s Covid experience, but in allowing inaccurate testimony to stand unchallenged and by promoting flawed and false presumptions, the inquiry will create a false record that risks distorting public health policy for decades.
Molly Kingsley is a founder and Ben Kingsley is the Head of Legal Affairs at children’s rights campaign group UsForThem. Find UsForThem on Substack.
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