Colin Powell, former general and secretary of state, dead at 84

Former Secretary of State and General Colin Powell died today at age 84 from complications of the coronavirus.

Powell was fully vaccinated.

Colin Powell Dies at 84 from COVID Complications — He Was Fully Vaccinated

His death announcement on Facebook sums up everything that is wrong with the political-elitist class in America today.

Despite being vaccinated, Powell succumbed to the virus. But this does not stop the elites from pushing their dangerous experimental vaccines on the American public. Even the notice posted on Powell’s Facebook page promotes the oversold injections.

You’ve gotta love those tyrants on Facebook!

We even have video on the extraordinary ineffectiveness of the COVID vaccines today.
At what point will the ruling class admit they were wrong and take a step back to reevaluate?

A video showing the shifting narrative in vaccine efficacy. A science world of the left. pic.twitter.com/BieFB1p4hy

— Americanka (@Americanka4) October 12, 2021

The post Colin Powell’s Facebook Page Announcement Sums Up Everything That’s Wrong with Political Ruling Class Today appeared first on The Gateway Pundit.

They believe in vaccines and voluntarily wanted to help end the Covid-19 pandemic. The nightmare for 12 year old Maddie de Gray and her family started after the second Pfizer ‘vaccine’ shot. She is only one of hundreds of thousands of cases. “On January 20 Maddie received her second does of the Pfizer Covid vaccine as a participant in the clinical trial for 12 to 15 year olds. All three of our kids who volunteered were excited to participate in the trial as a way to help us all return to normal life. My husband works in the medical field and I have a degree in electrical engineering. We are pro-vaccine and pro-science which is why we agreed to let Maddie and our two other children volunteer for the trial. Before Maddie got her final does of the vaccine she was a healthy 12 year old. . . . upon receiving the second shot Maddie immediately felt pain at the injection site and over the next 24 hours she developed severe chest and abdominal pain . . in the discharge papers from the children’s hospital ER that she went to the diagnosis stated adverse effect of vaccine initial encounter. . . Over the next two and a half months her abdominal, muscle and nerve pain became unbearable. She developed additional symptoms that included gastroparesis, nausea and vomiting, erratic blood pressure and heart rate, memory loss, she mixes up words, brain fog, headaches, dizziness, fainting, she fell and hit her head, and then seizures. She had developed verbal and motor ticks, had loss of feeling from the waist down and muscle weakness, drastic changes in her vision, urinary retention and loss of bladder control, severely irregular and heavy menstrual cycles and eventually she had to have an NG tube to get nutrition. . . . what I want to ask Maddie volunteered for the Pfizer trial. Why aren’t they researching in order to figure out why this happened so other people don’t have to go through this? Instead, they’re just saying it’s just mental.  . . . she did the right thing trying to help everyone else and they are not helping her.”

Researchers: Chien-Te Tseng ¹, Elena Sbrana, Naoko Iwata-Yoshikawa, Patrick C Newman, Tania Garron, Robert L Atmar, Clarence J Peters, Robert B Couch

Background:Severe acute respiratory syndrome (SARS) emerged in China in 2002 and spread to other countries before brought under control. Because of a concern for reemergence or a deliberate release of the SARS coronavirus, vaccine development was initiated. Evaluations of an inactivated whole virus vaccine in ferrets and nonhuman primates and a virus-like-particle vaccine in mice induced protection against infection but challenged animals exhibited an immunopathologic-type lung disease.

Conclusion: These SARS-CoV vaccines all induced antibody and protection against infection with SARS-CoV. However, challenge of mice given any of the vaccines led to occurrence of Th2-type immunopathology suggesting hypersensitivity to SARS-CoV components was induced. Caution in proceeding to application of a SARS-CoV vaccine in humans is indicated.

[Full Article At National Institutes Of Health]

Former world No. 25 Jeremy Chardy says he has a “series of problems” after taking the COVID-19 vaccine and his 2021 season is over. This summer, 34-year-old Chardy decided to get vaccinated and it didn’t work out well for him.

Chardy, now ranked at No. 73 in the world, claims he is unable to train and play. “Since I got my vaccine [between the Olympics and the US Open], I have a problem, I have a series of problems. As a result, I can’t train, I can’t play.

[…] I prefer to take more time to heal myself and be sure that, in the future, I won’t have any problems,” Chardy told L’Equipe.

[Tennis World]

Israel, the most Covid-19 ‘vaccinated’ country in the world is demonstrating that the mRNA shot has been a dismal failure. Not only are we having record adverse effects, it appears mass mRNA rollouts are causing more virulent and deadly Covid-19 mutants.

Vinay Prasad, an associate professor of medicine at the University of California, San Francisco, was among the critics of what unfolded.

“The CDC director, a political appointee, siding with the President, & his pre-ordained plan, against the advice of the ACIP advisors, with 0 [random controlled trials] measuring clinical outcomes & no idea of adverse events is not ‘doing one’s job’ it is politics [over] science, precisely what we feared,” he wrote on Twitter.

Geoff Porges, an analyst at SVB Leerink, wrote in a note that he expects several resignations from the advisory panel as a result of Walensky’s action.

Officials and panel members were united in supporting boosters for seniors. They say they’re needed because the efficacy of COVID-19 vaccines against severe disease and hospitalization is dropping among that population. . . .

[The Epoch Times]

Killing Fields refer to places where mass killings have occurred either during war or even by serial killers. With more deaths being reported to VAERS from the Covid-19 ‘vaccine’ than all other vaccines in the last thirty years combined, it has become clear we have created a medical killing field. What’s worse, it is known that systems like VAERS only capture about 1% of the adverse effects actually being experienced in the general public. In this video, Dr. Robert Malone, Inventor Of The mRNA ‘Vaccine’ Technology, Dr. Maria Gonzales, U.S. Department of Health & Jodi O’Malley, R.N., U.S. Department of Health discuss and comment on the Covid-19 ‘vaccine’ adverse effects.

Researchers: Priyamadhaba Behera ¹, Binod Kumar Patro ¹, Arvind Kumar Singh ¹, Pradnya Dilip Chandanshive ¹, Ravikumar S R ¹, Somen Kumar Pradhan ¹, Siva Santosh Kumar Pentapati ¹, Gitanjali Batmanabane ², Prasanta Raghab Mohapatra ³, Biswa Mohan Padhy ⁴, Shakti Kumar Bal ³, Sudipta Ranjan Singh ⁵, Rashmi Ranjan Mohanty ⁶

Background: Ivermectin is one among several potential drugs explored for its therapeutic and preventive role in SARS-CoV-2 infection. The study was aimed to explore the association between ivermectin prophylaxis and the development of SARS-CoV-2 infection among healthcare workers.

Conclusion: Two-dose ivermectin prophylaxis at a dose of 300 μg/kg with a gap of 72 hours was associated with a 73% reduction of SARS-CoV-2 infection among healthcare workers for the following month. Chemoprophylaxis has relevance in the containment of pandemic.

[National Institutes of Health]

Published: 05th November 2020 12:55 AM  |   Last Updated: 05th November 2020 12:55 AM

BHUBANESWAR: In a significant finding, two-dose Ivermectin prophylaxis has led to 73 per cent
reduction in COVID-19 infection among healthcare workers (HCWs), who are more likely to contract the virus given their nature of job.

“Earlier, at least 20 to 25 HCWs were getting infected with the virus daily. After the workers started taking Ivermectin, the number of infection has come down to one or two per day,” Dr Batmanabane said.

“Considering the fact that Ivermectin had been shown to have diverse mechanisms by which it successfully attacks the SARS-CoV-2, we decided to use it. The Ivermectin has a proven safety profile as a safe drug which has been used for many decades. The encouraging results of a study from Egypt prompted us to explore its role as prophylaxis for HCWs,” she said. . . .

[New India Express]

Following an intense daylong public discussion, a panel of scientific advisors to the U.S. Food and Drug Administration (FDA) today voted 16 to 2 against recommending a third shot of Pfizer’s COVID vaccine for people 16 and older.

The Biden administration has been hoping the FDA would approve a third shot of the Pfizer vaccine in time to begin rolling out boosters for Pfizer recipients next week, the New York Times reported.

The vote came after a sharp debate in which many of the panel’s independent experts, including infectious disease doctors and statisticians, challenged whether the data justified a broad rollout of extra shots when the vaccines appear to still offer robust protection against severe COVID-19 disease and hospitalization, at least in the U.S.

“It’s unclear that everyone needs to be boosted, other than a subset of the population that clearly would be at high risk for serious disease,” said Dr. Michael G. Kurilla, a committee member and official at the National Institutes of Health.

The issue of whether or not to approve boosters has become increasingly contentious, dividing scientists, both outside and inside the FDA, including two scientists who recently announced they are leaving the agency because of pressure from the Biden administration to approve boosters, citing the lack of data to support a third shot.

“It’s a welcome sight to see actual deliberations in meetings about vaccine booster shots at the FDA,” said Mary Holland, president of Children’s Health Defense. “It’s encouraging that a panel of experts stood up to political and corporate pressure based on the lack of convincing data for safety and efficacy of boosters.”

Holland added:

“One can only hope the FDA and Centers for Disease Control and Prevention panels will continue to engage in vigorous debate about vaccine science and medicine.”

As The Hill reported, the advisory panel’s vote is not binding, so the FDA doesn’t have to accept the results. But if the agency doesn’t, it will raise significant questions of political interference and pit agency scientists against political officials who signed off on the booster plan.

In an unusual move last month, Biden and top health officials, including Surgeon General Vicek Murthy, acting FDA Commissioner Dr. Janet Woodcock and CDC  Director Dr, Rochelle Walensky, publicly announced a booster shot program would begin the week of Sept. 20, well before the FDA and CDC examined the evidence.

On Thursday, FDA scientists had expressed skepticism about the need for Pfizer COVID vaccine booster shots in a report released Wednesday.

In 23-page report, FDA officials said, based on their analysis of data submitted by Pfizer and BioNTech, they could not yet take a stance on whether to recommend COVID boosters for the general public.

SIGN UP #TheDefender: https://t.co/zL66Edfiw5https://t.co/dvbbGv87R2

— Robert F. Kennedy Jr (@RobertKennedyJr) September 16, 2021

The 23-page report analyzed data submitted by Pfizer and BioNTech as part of the drugmakers’ request for authorization for their vaccine to be given as a booster shot in people 16 years and older.

[Children’s Health Defense]

As of September 2021, the standard protocol for Covid-19 patients is still to be sent home and when their lips turn blue from low oxygen, they are hospitalized. Knowing they’re at risk of being hospitalized Americans are desperately seeking for some sort of treatment.

Dr. Malone discusses the bizarre amount of misinformation that is being spread about perfectly safe and useful medications, such as the Nobel Prize winning drug for human use, Ivermectin.

What ever happened to the Liberal cry that government should not come between a patient and her doctor?

Sweden became the second European Union country to ban Israeli residents from entry due to a rise in COVID-19 cases in Israel, despite the country being one of the most vaccinated countries in the world.

Portugal on Wednesday became the first EU country to ban travel from Israel due to a rise in cases. Both countries are following the EU’s recommendation to remove Israel from its list of green countries.

Sweden also banned the entry of citizens from the United States, Kosovo, Lebanon, Montenegro, and North Macedonia.

Interior Minister Mikael Damberg told news outlets that the sharp increases in COVID-19 cases in Israel, the United States, and other countries are the reason why they were removed from Sweden’s travel ban exemption. Despite Israel’s mass vaccination campaign, the virus has continued to spread, Damberg said.

According to a news release from the Swedish government, it will reintroduce a travel ban on Israel, the U.S., and other countries starting from Sept. 6.

“Regarding foreign citizens travelling to Sweden from the US, Israel, Kosovo, Lebanon, Montenegro, and North Macedonia as of 6 September, only those covered by another exemption from the entry ban may enter Sweden,” said the release. “This could concern foreign citizens who have residence permits in Sweden, have particularly urgent needs or are to carry out essential functions, and who can also present a negative COVID-19 test. The negative COVID-19 test result may not be older than 48 hours. This requirement applies to foreign citizens aged 18 and older, with certain exemptions.”

The Swedish government said it is following the EU’s guidelines on removing those countries from its safe travel list, and it said the directive will be revisited at a later date.

Several Israeli politicians criticized the EU’s directive and Portugal’s mandate. . . .

[The Epoch Times]

Breakthrough cases reach majority levels in some jurisdictions but numbers elude CDC.

“I’m not going to arm wrestle with the administration about where to put you,” Dr. C., a highly skilled gastroenterologist, said gently to my friend who was in bed in a triage room in the ER. “We just want to get you into a bed so we can figure out what’s wrong and get you treated.”

We were at our small town’s hospital. No one was sure why, but my friend had not been able to keep anything more than a handful of raspberries down since a complicated surgery for a chronic health condition three weeks before. Dehydrated and unable to eat, my friend had been violently vomiting after taking just a sip of water or sucking on an ice chip, and had lost nearly twenty-five pounds.

I was by my husband’s side when he had a gallbladder attack so severe that it left his hands shaking. I’ve had three unmedicated childbirths and attended many more, both as a journalist and a patient advocate. Still, I’ve never seen a human in so much pain.

Diagnosed with a Pancreas Disorder, Admitted as a COVID Patient

After a battery of testing, my friend was diagnosed with pancreatitis. But it was easier for the hospital bureaucracy to register the admission as a COVID case.

Let me explain. This patient had none of the classic symptoms of COVID: No shortness of breath, no fever, no chills, no congestion, no loss of sense of smell or taste, no neurological issues. The only COVID symptoms my friend had were nausea and fatigue, which could also be explained by the surgery. However, nearly three weeks earlier, a COVID test had come back positive.

The mainstream media is reporting that severe COVID cases are mainly among unvaccinated people. An Associated Press headline from June 29 reads: “Nearly all COVID deaths in US are now among unvaccinated.” Another, from the same date: “Vast majority of ICU patients with COVID-19 are unvaccinated, ABC News survey finds.”

Is that what’s really going on? It’s certainly not the case in Israel, the first country to fully vaccinate a majority of its citizens against the virus. Now it has one of the highest daily infection rates and the majority of people catching the virus (77 percent to 83 percent, depending on age) are already vaccinated, according to data collected by the Israeli government.

After carefully reviewing the available data, including the safety and efficacy profiles of the mRNA vaccines, my friend had taken a cautious approach. Though a medical doctor who gives vaccines in the office every day, my friend opted to wait and see. According to WebMD, a “huge number” of frontline hospital workers have also chosen not to get the vaccine. Indeed, various news reports, from California to New York, confirm that up to 40 percent of health care workers have decided the risks of the vaccines do not outweigh the benefits.

After admission, I spoke to the nurse on the COVID ward. She was suited up in a plastic yellow disposable gown, teal gloves, and two masks underneath a recirculating personal respiratory system that buzzed so loudly she could barely hear. The nurse told me that she had gotten both vaccines but she was feeling worried: “Two thirds of my patients are fully vaccinated,” she said.

[The Epoch Times – Full Article]

Published online 2021 Apr 22.

Title: Review of the Emerging Evidence Demonstrating the Efficacy of Ivermectin in the Prophylaxis and Treatment of COVID-19

Researchers: Pierre Kory, MD,^1,* Gianfranco Umberto Meduri, MD,² Joseph Varon, MD,³Jose Iglesias, DO,⁴ and Paul E. Marik, MD⁵

Conclusions: Meta-analyses based on 18 randomized controlled treatment trials of ivermectin in COVID-19 have found large, statistically significant reductions in mortality, time to clinical recovery, and time to viral clearance. Furthermore, results from numerous controlled prophylaxis trials report significantly reduced risks of contracting COVID-19 with the regular use of ivermectin. Finally, the many examples of ivermectin distribution campaigns leading to rapid population-wide decreases in morbidity and mortality indicate that an oral agent effective in all phases of COVID-19 has been identified.

[Full Article At NIH]

So the FDA warns against using Hydroxychloroquine and Zinc, Fauci reluctantly says Vitamin D3 may help and now the FDA and Medical Boards are lined up against Ivermectin. Perhaps it’s because they reduce death and disease without an mRNA ‘vaccine’ as published at the National Institutes of Health.

Published online 2021 Aug 3.

Title: Ivermectin: a multifaceted drug of Nobel prize-honoured distinction with indicated efficacy against a new global scourge, COVID-19

Researchers: A.D. Santin,¹ D.E. Scheim,^2,∗ P.A. McCullough,³ M. Yagisawa,⁴ and T.J. Borody⁵

Abstract, Partial, Paragraph 1 : “Since March 2020, when IVM was first used against a new global scourge, COVID-19, more than 20 randomized clinical trials (RCTs) have tracked such inpatient and outpatient treatments. Six of seven meta-analyses of IVM treatment RCTs reporting in 2021 found notable reductions in COVID-19 fatalities, with a mean 31% relative risk of mortality vs. controls. During mass IVM treatments in Peru, excess deaths fell by a mean of 74% over 30 days in its ten states with the most extensive treatments.”

[Full Article, National Institutes of Health]

In a very telling interview, Dr. Robert Malone, inventor of the mRNA ‘vaccine’ technology, explains that governments have been denying that there are any issues with the mRNA ‘vaccine’, how long Covid symptoms match up with mRNA adverse reaction symptoms, and finally, how ‘masking’ causes mRNA adverse reactions to be missed by doctors and researchers.

Title: Ivermectin for Prevention and Treatment of COVID-19 Infection: A Systematic Review, Meta-analysis, and Trial Sequential Analysis to Inform Clinical Guidelines

Researchers: Andrew Bryant, MSc,^1,* Theresa A. Lawrie, MBBCh, PhD,²Therese Dowswell, PhD,² Edmund J. Fordham, PhD,² Scott Mitchell, MBChB, MRCS,³ Sarah R. Hill, PhD,¹ and Tony C. Tham, MD, FRCP⁴

Conclusion: Moderate-certainty evidence finds that large reductions in COVID-19 deaths are possible using ivermectin. Using ivermectin early in the clinical course may reduce numbers progressing to severe disease. The apparent safety and low cost suggest that ivermectin is likely to have a significant impact on the SARS-CoV-2 pandemic globally.

[Full Article: Ivermectin for Prevention and Treatment of COVID-19 Infection: A Systematic Review, Meta-analysis, and Trial Sequential Analysis to Inform Clinical Guidelines]

Once again, Dr. Robert Malone, inventor of the mRNA ‘vaccine’ technology hits the nail on the head. Not only is there Ivermectin, there is a whole host of therapeutics going unused for treating Covid-19 to reduce death and disease.

“Discovered in the late-1970s, the pioneering drug ivermectin, a dihydro derivative of avermectin—originating solely from a single microorganism isolated at the Kitasato Intitute, Tokyo, Japan from Japanese soil—has had an immeasurably beneficial impact in improving the lives and welfare of billions of people throughout the world. Originally introduced as a veterinary drug, it kills a wide range of internal and external parasites in commercial livestock and companion animals. It was quickly discovered to be ideal in combating two of the world’s most devastating and disfiguring diseases which have plagued the world’s poor throughout the tropics for centuries. It is now being used free-of-charge as the sole tool in campaigns to eliminate both diseases globally. It has also been used to successfully overcome several other human diseases and new uses for it are continually being found. This paper looks in depth at the events surrounding ivermectin’s passage from being a huge success in Animal Health into its widespread use in humans, a development which has led many to describe it as a “wonder” drug.” (Introduction To: Ivermectin, ‘Wonder drug’ from Japan: the human use perspective)

[Full Article On US National Library of Medicine, National Institutes of Health]

When Dr. Ryan Cole decided to become a physician, he took an oath to protect his patients and to treat them to the best of his ability.

Cole, CEO of Cole Diagnostics and a board-certified dermatopathologist trained at the Mayo Clinic, said he has a motto when it comes to the coronavirus: Test and treat — and treat earlier with the Delta variant.

Cole told Children’s Health Defense Chairman Robert F. Kennedy, Jr., on the “RFK Jr. The Defender Podcast,” that while the Delta variant is spreading “like a wildfire right now,” data show it’s less deadly.

Cole, who reviews the lab tests of about 30,000 patients a year at his independent lab in Boise, Idaho, said he uses a multi-drug approach when treating patients for COVID.

Some of the drugs he’s found effective include ivermectin — an antiparasitic drug proven beneficial for treating SARS-CoV-2 — hydroxychloroquine, steroids, and the cholesterol drug fenofibrate and fluvoxamine for patients with neural symptoms.

Monoclonal antibodies are a good treatment, too, said Cole.

Treatments using monoclonal antibodies are “parked in infusion centers and emergency rooms around the country,” said Cole. “But there are crickets about this drug that decreases death and hospitalization by 50%.”

Cole told Kennedy his first COVID patient was his brother, who was considered “high risk” for the virus due to his weight. He was on the way to the emergency room when I told him, “No, you’re going to the pharmacy,” said Cole.

Cole said his brother had chest pains on a nine out of 10 level before he called in a prescription for ivermectin. Six hours later, his pain was down to a two, and by the next morning, his oxygen levels had risen from 80 to 98.

Ivermectin saved my brother’s life, said Cole.

Cole, who also treated his 78-year-old mother and 83-year-old father, said out of the hundreds of patients he’s treated, zero have gone to the hospital.

“Test and treat early,” said Cole. “Not treating early is doing harm. It’s a sin of omission by not treating.”

Cole said if you do get COVID, finding a good doctor to treat you is key. He pointed to several websites that provide tele-health services including Frontline MDs, My Free Doctor and America’s Frontline Doctors.

Viruses aren’t “politically red, blue or even purple,” said Cole. “This is about humanity” and doing the “proper thing by our fellow citizens.”

Listen to the interview:

A letter this week to UK Prime Minister Boris Johnson and other UK government officials, signed by more than 130 UK medical professionals, accused the government of mishandling its response to the COVID pandemic, resulting in “massive, permanent and unnecessary harm” to the country.

The letter, “Our Grave Concerns About the Handling of the COVID Pandemic by Governments of the Nations of the UK,” outlined 10 ways in which the authors argued UK government policies not only failed to protect citizens, but in many cases caused additional, unnecessary harm.

The letter’s 10 lead authors wrote:

“We write as concerned doctors, nurses and other allied healthcare professionals with no vested interest in doing so. To the contrary, we face personal risk in relation to our employment for doing so and / or the risk of being personally ‘smeared’ by those who inevitably will not like us speaking out.”

The authors accused government officials of failing to measure the harms of lockdown policies, of exaggerating the virus’ threat and of improper mass testing of children.

They wrote:

“Repeated testing of children to find asymptomatic cases who are unlikely to spread virus, and treating them like some sort of biohazard is harmful, serves no public health purpose and must stop.”

The letter also called out officials for actively suppressing discussion of early treatment using protocols being successfully deployed elsewhere, and said vaccination of the entire adult population should never have been a prerequisite for ending restrictions.

The authors concluded:

“The UK’s approach to COVID has palpably failed. In the apparent desire to protect one vulnerable group — the elderly — the implemented policies have caused widespread collateral and disproportionate harm to many other vulnerable groups, especially children.”

In addition to Johnson, the letter was addressed to Nicola Sturgeon, First Minister for Scotland; Mark Drakeford, First Minister for Wales; Paul Givan, First Minister for Northern Ireland; Sajid Javid, Health Secretary; Chris Whitty, Chief Medical Officer; and Dr. Patrick Vallance, Chief Scientific Officer.

Read the full letter:

22 August 2021

Dear Sirs and Madam,

Our grave concerns about the handling of the COVID pandemic by Governments of the Nations of the UK.

We write as concerned doctors, nurses, and other allied healthcare professionals with no vested interest in doing so. To the contrary, we face personal risk in relation to our employment for doing so and / or the risk of being personally “smeared” by those who inevitably will not like us speaking out.

We are taking the step of writing this public letter because it has become apparent to us that:

• The  Government (by which we mean the UK government and three devolved governments/administrations and associated government advisors and agencies such as the CMOs, CSA, SAGE, MHRA, JCVI, Public Health services, Ofcom etc, hereinafter “you” or the “Government”) have based the handling of the COVID pandemic on flawed assumptions.
• These have been pointed out to you by numerous individuals and organisations.
• You have failed to engage in dialogue and show no signs of doing so. You have removed from people fundamental rights and altered the fabric of society with little debate in Parliament. No minister responsible for policy has ever appeared in a proper debate with anyone with opposing views on any mainstream media channel.
• Despite being aware of alternative medical and scientific viewpoints you have failed to ensure an open and full discussion of the pros and cons of alternative ways of managing the pandemic.
• The pandemic response policies implemented have caused massive, permanent and unnecessary harm to our nation, and must never be repeated.
• Only by revealing the complete lack of widespread approval among healthcare professionals of your policies will a wider debate be demanded by the public.

In relation to the above, we wish to draw attention to the following points. Supporting references can be provided upon request.

1. No attempt to measure the harms of lockdown policies

The evidence of disastrous effects of lockdowns on the physical and mental health of the population is there for all to see. The harms are massive, widespread, and long lasting. In particular, the psychological impact on a generation of developing children could be lifelong.

It is for this reason that lockdown policies were never part of any pandemic

preparedness plans prior to 2020. In fact, they were expressly not recommended in WHO documents, even for severe respiratory viral pathogens and for that matter neither were border closures, face coverings, and testing of asymptomatic individuals. There has been such an inexplicable absence of consideration of the harms caused by lockdown policy it is difficult to avoid the suspicion that this is willful avoidance.

The introduction of such policies was never accompanied by any sort of risk/benefit analysis. As bad as that is, it is even worse that after the event when plenty of data became available by which the harms could be measured, only perfunctory attention to this aspect of pandemic planning has been afforded. Eminent professionals have repeatedly called for discourse on these health impacts in press-conferences but have been universally ignored.

What is so odd, is that the policies being pursued before mid-March 2020 (self-isolation of the ill and protection of the vulnerable, while otherwise society continued close to normality) were balanced, sensible and reflected the approach established by consensus prior to 2020. No cogent reason was given then for the abrupt change of direction from mid-March 2020 and strikingly none has been put forward at any time since.

2. Institutional nature of COVID

It was actually clear early on from Italian data that COVID (the disease, as opposed to SARS-Cov-2 infection or exposure) was largely a disease of institutions. Care home residents comprised around half of all deaths, despite making up less than 1% of the population. Hospital infections are the major driver of transmission rates as was the case for both SARS1 and MERS.

Transmission was associated with hospital contact in up to 40% of cases in the first wave in Spring 2020 and in 64% in winter 2020/2021.

Severe illness among healthy people below 70 years old did occur (as seen with flu pandemics) but was extremely rare.

Despite this, no early, aggressive and targeted measures were taken to protect care homes; to the contrary, patients were discharged without testing to homes where staff had inadequate PPE, training and information. Many unnecessary deaths were caused as a result.

Preparations for this coming winter, including ensuring sufficient capacity and preventative measures such as ventilation solutions, have not been prioritised.

3. The exaggerated nature of the threat

Policy appears to have been directed at systematic exaggeration of the number of deaths which can be attributed to COVID. Testing was designed to find every possible ‘case’ rather than focusing on clinically diagnosed infections and the resulting exaggerated case numbers fed through to the death data with large numbers of people dying ‘with COVID’ and not ‘of COVID’ where the disease was the underlying cause of death.

The policy of publishing a daily death figure meant the figure was based entirely on the PCR test result with no input from treating clinicians. By including all deaths within a time period after a positive test, incidental deaths, with but not due to COVID, were not excluded thereby exaggerating the nature of the threat.

Moreover, in headlines reporting the number of deaths, a categorisation by age was not included. The average age of a COVID-labelled death is 81 for men and 84 for women, higher than the average life expectancy when these people were born.

This is a highly relevant fact in assessing the societal impact of the pandemic. Death in old age is a natural phenomenon. It cannot be said that a disease primarily affecting the elderly is the same as one which affects all ages, and yet the government’s messaging appears designed to make the public think that everyone is at equal risk.

Doctors were asked to complete death certificates in the knowledge that the deceased’s death had already been recorded as a COVID death by the Government. Since it would be virtually impossible to find evidence categorically ruling out COVID as a contributory factor to death, once recorded as a “COVID death” by the government, it was inevitable that it would be included as a cause on the death certificate.

Diagnosing the cause of death is always difficult and the reduction in post mortems will have inevitably resulted in increased inaccuracy. The fact that deaths due to non-COVID causes actually moved into a substantial deficit (compared to average) as COVID-labelled deaths rose (and this was reversed as COVID-labelled deaths fell) is striking evidence of over-attribution of deaths to COVID.

The overall all-cause mortality rate from 2015-2019 was unusually low and yet these figures have been used to compare to 2020 and 2021 mortality figures which has made the increased mortality appear unprecedented. Comparisons with data from earlier years would have demonstrated that the 2020 mortality rate was exceeded in every year prior to 2003 and is unexceptional as a result.

Even now COVID cases and deaths continue to be added to the existing total without proper rigour such that overall totals grow ever larger and exaggerate the threat. No effort has been made to count totals in each winter season separately which is standard practice for every other disease.

You have continued to adopt high-frequency advertising through publishing and broadcast media outlets to add to the impact of “fear messaging”. The cost of this has not been widely published, but government procurement websites reveal it to be immense — hundreds of millions of pounds.

The media and government rhetoric is now moving onto the idea that “Long Covid” is going to cause major morbidity in all age groups including children, without having a discussion of the normality of postviral fatigue which lasts upwards of 6 months. This adds to the public fear of the disease, encouraging vaccination amongst those who are highly unlikely to suffer any adverse effects from COVID.

4. Active suppression of discussion of early treatment using protocols being successfully deployed elsewhere

The harm caused by COVID and our response to it should have meant that advances in prophylaxis and therapeutics for COVID were embraced. However, evidence on successful treatments has been ignored or even actively suppressed.

For example, a study in Oxford published in February 2021 demonstrated that inhaled Budesonide could reduce hospitalisations by 90% in low risk patients and a publication in April 2021 showed that recovery was faster for high risk patients too. However, this important intervention has not been promoted.

Dr. Tess Lawrie, of the Evidence Based Medical Consultancy in Bath, presented a thorough analysis of the prophylactic and therapeutic benefits of Ivermectin to the government in January 2021. More than 24 randomised trials with 3,400 people have demonstrated a 79-91% reduction in infections and a 27-81% reduction in deaths with Ivermectin.

Many doctors are understandably cautious about possible over-interpretation of the available data for the drugs mentioned above and other treatments, although it is to be noted that no such caution seems to have been applied in relation to the treatment of data around the government’s interventions (eg the effectiveness of lockdowns or masks) when used in support of the government’s agenda.

Whatever one’s view on the merits of these repurposed drugs, it is totally unacceptable that doctors who have attempted to merely open discussion about the potential benefits of early treatments for COVID have been heavily and inexplicably censored. Knowing that early treatments which could reduce the risk of requiring hospitalisation might be available would alter the entire view held by many professionals and lay people alike about the threat posed by COVID, and therefore the risk / benefit ratio for vaccination, especially in younger groups.

5. Inappropriate and unethical use of behavioural science to generate unwarranted fear

Propagation of a deliberate fear narrative (confirmed through publicly accessible government documentation) has been disproportionate, harmful and counterproductive. We request that it should cease forthwith.

To give just one example, the government’s face covering policies seem to have been driven by behavioural psychology advice in relation to generating a level of fear necessary for compliance with other policies.

Those policies do not appear to have been driven by reason of infection control, because there is no robust evidence showing that wearing a face covering (particularly cloth or standard surgical masks) is effective against transmission of airborne respiratory pathogens such as SARS-Cov-2.

Several high profile institutions and individuals are aware of this and have advocated against face coverings during this pandemic only inexplicably to reverse their advice on the basis of no scientific justification of which we are aware. On the other hand there is plenty of evidence suggesting that mask wearing can cause multiple harms, both physical and mental.

This has been particularly distressing for the nation’s school children who have been encouraged by government policy and their schools to wear masks for long periods at school.

Finally, the use of face coverings is highly symbolic and thus counterproductive in making people feel safe. Prolonged wearing risks becoming an ingrained safety behaviour, actually preventing people from getting back to normal because they erroneously attribute their safety to the act of mask wearing rather than to the remote risk, for the vast majority of healthy people under 70 years old, of catching the virus and becoming seriously unwell with COVID.

6. Misunderstanding of the ubiquitous nature of mutations of newly emergent viruses

The mutation of any novel virus into newer strains — especially when under selection pressure from abnormal restrictions on mixing and vaccination — is normal, unavoidable and not something to be concerned about. Hundreds of thousands of mutations of the original Wuhan strain have already been identified.

Chasing down every new emergent variant is counterproductive, harmful and totally unnecessary and there is no convincing evidence that any newly identified variant is any more deadly than the original strain.

Mutant strains appear simultaneously in different countries (by way of ‘convergent evolution’) and the closing of national borders in attempts to prevent variants travelling from one country to another serves no significant infection control purpose and should be abandoned.

7. Misunderstanding of asymptomatic spread and its use to promote public compliance with restrictions

It is well-established that asymptomatic spread has never been a major driver of a respiratory disease pandemic and we object to your constant messaging implying this, which should cease forthwith.

Never before have we perverted the centuries-old practice of isolating the ill by instead isolating the healthy. Repeated mandates to healthy, asymptomatic people to self-isolate, especially school children, serves no useful purpose and has only contributed to the widespread harms of such policies.

In the vast majority of cases healthy people are healthy and cannot transmit the virus and only sick people with symptoms should be isolated.

The government’s claim that one in three people could have the virus has been shown to be mutually inconsistent with the ONS data on prevalence of disease in society, and the sole effect of this messaging appears to have been to generate fear and promote compliance with government restrictions.

The government’s messaging to ‘act as if you have the virus’ has also been unnecessarily fear-inducing given that healthy people are extremely unlikely to transmit the virus to others.

The PCR test, widely used to determine the existence of ‘cases’, is now indisputably acknowledged to be unable reliably to detect infectiousness. The test cannot discriminate between those in whom the presence of fragments of genetic material partially matching the virus is either incidental (perhaps because of past infection), or is representative of active infection, or is indicative of infectiousness.

Yet, it has been used almost universally without qualification or clinical diagnosis to justify lockdown policies and to quarantine millions of people needlessly at enormous cost to health and well-being and to the country’s economy.

Countries that have removed community restrictions have seen no negative consequences which can be attributed to the easing. Empirical data from many countries demonstrates that the rise and fall in infections is seasonal and not due to restrictions or face coverings.

The reason for reduced impact of each successive wave is that: (1) most people have some level of immunity either through prior immunity or immunity acquired through exposure; (2) as is usual with emergent new viruses, mutation of the virus towards strains causing milder disease appears to have occurred.

Vaccination may also contribute to this although its durability and level of protection against variants is unclear.

The government appears to be talking of “learning to live with COVID” while apparently practicing by stealth a “zero COVID” strategy which is futile and ultimately net-harmful.

8. Mass testing of healthy children

Repeated testing of children to find asymptomatic cases who are unlikely to spread virus, and treating them like some sort of biohazard is harmful, serves no public health purpose and must stop.

During Easter term, an amount equivalent to the cost of building one District General Hospital was spent weekly on testing schoolchildren to find a few thousand positive ‘cases’, none of which was serious as far as we are aware.

Lockdowns are in fact a far greater contributor to child health problems, with record levels of mental illness and soaring levels of non-COVID infections being seen, which some experts consider to be a result of distancing resulting in deconditioning of the immune system.

9. Vaccination of the entire adult population should never have been a prerequisite for ending restrictions

Based merely on early “promising” vaccine data, it is clear that the Government decided in summer 2020 to pursue a policy of viral suppression within the entire population until vaccination was available (which was initially stated to be for the vulnerable only, then later changed — without proper debate or rigorous analysis — to the entire adult population).

This decision was taken despite massive harms consequent to continued lockdowns which were either known to you or ought to have been ascertained so as to be considered in the decision making process.

Moreover, a number of principles of good medical practice and previously unimpeachable ethical standards have been breached in relation to the vaccination campaign, meaning that in most cases, whether the consent obtained can be truly regarded as “fully informed” must be in serious doubt:

• The use of coercion supported by an unprecedented media campaign to persuade the public to be vaccinated, including threats of discrimination, either supported by the law or encouraged socially, for example in co-operation with social media platforms and dating apps.
• The omission of information permitting individuals to make a fully informed choice, especially in relation to the experimental nature of the vaccine agents, extremely low background COVID risk for most people, known occurrence of short-term side-effects and unknown long-term effects.

Finally, we note that the Government is seriously considering the possibility that these vaccines — which have no associated long-term safety data — could be administered to children on the basis that this might provide some degree of protection to adults. We find that notion an appalling and unethical inversion of the long-accepted duty falling on adults to protect children.

10. Over-reliance on modeling while ignoring real-world data

Throughout the pandemic, decisions seem to have been taken utilising unvalidated models produced by groups who have what can only be described as a woeful track record, massively overestimating the impact of several previous pandemics.

The decision-making teams appear to have very little clinical input and, as far as is ascertainable, no clinical immunology expertise.

Moreover, the assumptions underlying the modeling have never been adjusted to take into account real-world observations in the UK and other countries.

It is an astonishing admission that, when asked whether collateral harms had been considered by SAGE, the answer given was that it was not in their remit — they were simply asked to minimise COVID impact. That might be forgivable if some other advisory group was constantly studying the harms side of the ledger, yet this seems not to have been the case.

Conclusions

The UK’s approach to COVID has palpably failed. In the apparent desire to protect one vulnerable group — the elderly — the implemented policies have caused widespread collateral and disproportionate harm to many other vulnerable groups, especially children.

Moreover your policies have failed in any event to prevent the UK from notching up one of the highest reported death rates from COVID in the world.

Now, despite very high vaccination rates and the currently very low COVID death and hospitalisation rates, policy continues to be aimed at maintaining a population handicapped by extreme fear with restrictions on everyday life prolonging and deepening the policy-derived harms.

To give just one example, NHS waiting lists now stand at 5.1m officially, with — according to the previous Health Secretary — a likely further 7m who will require treatment not yet presented. This is unacceptable and must be addressed urgently.

In short, there needs to be a sea change within the Government which must now pay proper attention to those esteemed experts outside its inner circle who are sounding these alarms.

As those involved with healthcare, we are committed to our oath to “first do no harm”, and we can no longer stand by in silence observing policies which have imposed a series of supposed “cures” which are in fact far worse than the disease they are supposed to address.

The signatories of this letter call on you, in Government, without further delay to widen the debate over policy, consult openly with groups of scientists, doctors, psychologists and others who share crucial, scientifically-valid and evidence-based alternative views and to do everything in your power to return the country as rapidly as possible to normality with the minimum of further damage to society.

Yours sincerely,

Dr Jonathan Engler, MB ChB LLB (Hons) DipPharmMed

Professor John A Fairclough, BM BS B Med Sci FRCS FFSEM,  Consultant Surgeon, ran vaccination program for a Polio Outbreak, Past President BOSTA, for Orthopaedic Surgeons, Faculty member FFSEM

Mr. Tony Hinton, MB ChB, FRCS, FRCS(Oto), Consultant Surgeon

Dr. Renee Hoenderkamp, BSc (Hons) MBBS MRCGP, General Practitioner

Dr. Ros Jones, MBBS, MD, FRCPCH, retired consultant paediatrician

Mr. Malcolm Loudon, MB ChB MD FRCSEd FRCS (Gen Surg) MIHM VR

Dr. Geoffrey Maidment, MBBS, MD, FRCP, retired consultant physician

Dr. Alan Mordue, MB ChB, FFPH (ret), Retired Consultant in Public Health Medicine

Mr. Colin Natali, BSc(Hons), MBBS FRCS FRCS(Orth), Consultant Spine Surgeon

Dr. Helen Westwood, MBChB MRCGP DCH DRCOG, General Practitioner

Click here, for the complete list of signatories.