Below is a letter signed by 76 doctors in the UK, to the Medical and Healthcare products Regulatory Agency (MHRA) and other U.K. Government officials. This letter lays out comprehensive reasons why the recent U.S. FDA decision authorizing COVID vaccinations in infants and young children must not happen in the UK. The letter is well-sourced and accurate. Let us hope that mainstream media here in the USA and the UK report on this letter in an unbiased fashion.
I have not changed or added anything to this letter except that everything I write or copy and paste is put through a professional grammar-checking software, so some words and sentences may be corrected or changed. They shall mean and seam the same and so not alter the meaning of the letter in any way.
the letter continues)
We are writing to you urgently concerning the announcement that the FDA has granted an Emergency Use Authorization for both Pfizer and Moderna COVID-19 vaccines in preschool children.
We would urge you to consider very carefully the move to vaccinate ever younger children against SARS-CoV-2, despite the gradual but significant reducing virulence of successive variants, the increasing evidence of rapidly waning vaccine efficacy, the increasing concerns over long-term vaccine harms, and the knowledge that the vast majority of this young age group have already been exposed to SARS-CoV-2 repeatedly and have demonstrably effective immunity. Thus, the balance of benefit and risk which supported the rollout of mRNA vaccines to the elderly and vulnerable in 2021 is inappropriate for small children in 2022.
We also strongly challenge the addition of COVID-19 vaccination into the routine childhood immunization program despite no demonstrated clinical need, known and unknown risks (see below) and the fact that these vaccines still have only conditional marketing authorization.
It is noteworthy that the Pfizer documentation presented to the FDA has huge gaps in the evidence provided:
The protocol was changed mid-trial. The original two-dose schedule exhibited poor immunogenicity with efficacy far below the required standard. A third dose was added by which time many of the original placebo recipients had been vaccinated.
There was no statistically significant difference between the placebo and vaccinated groups in either the 6–23-month age group or the 2-4-year-olds, even after the third dose. Astonishingly, the results were based on just three participants in the younger age group (one vaccinated and two placebo) and just seven participants in the older 2–4-year-olds (two vaccinated and five placebo). Indeed, for the younger age group the confidence intervals ranged from minus-367% to plus-99%. The manufacturer stated that the numbers were too low to draw any confident conclusions. Moreover, these limited numbers come only from children infected more than seven days after the third dose.
Over the whole period from the first dose onwards (see page 39 Tables 19 and 20), there were a total of 225 infected children in the vaccinated arm and 150 in the placebo arm, giving a calculated vaccine efficacy of only 25% (14% for the 6-23 months, and 33% for 2-4s).
The additional immunogenicity studies against Omicron, requested by the FDA, only involved a total of 66 children tested one month after the third dose (see page 35).
It is incomprehensible that the FDA considered that this represents sufficient evidence on which to base a decision to vaccinate healthy children. When it comes to safety, the data are even thinner: only 1,057 children, some already unblinded, were followed for just two months. It is noteworthy that Sweden and Norway are not recommending the vaccine for 5-11s and Holland is not recommending it for children who have already had COVID-19. The director of the Danish Health and Medicines Authority stated recently that with what is now known, the decision to vaccinate children was a mistake.
We summarize below the overwhelming arguments against this vaccination.
A. The extremely low risk from COVID-19 in young children
In the whole of 2020 and 2021, not a single child aged 1-9 died where COVID-19 was the sole diagnosis on the death certificate, according to ONS data.
A detailed study in England from March 1st 2020 to March 1st 2021 found only six children under 18 years died with no co-morbidities. There were no deaths aged 1-4 years.
Since the arrival of the Omicron variant, infections have been generally much milder. That is also true for unvaccinated under-5s.
By June 2022 it is now estimated that 89% of 1-4-year-olds had already had SARS-CoV-2 infection.
Recent data from Israel show excellent long-lasting immunity following infection in children, especially in 5-11s.
B. Poor vaccine efficacy
In adults, it has become apparent that vaccine efficacy wanes steadily over time, necessitating boosters at regular intervals. Specifically, vaccine efficacy has waned more rapidly against the latest Omicron variants.
In children, vaccine efficacy has waned more rapidly in 5-11s than in 12-17s, possibly related to the lower dose used in the pediatric formulation. One study from New York showed efficacy against Omicron falling to only 12% by 4-5 weeks and to negative values by 5-6 weeks post the second dose.
In the Pfizer 0-4s trial, the efficacy after two doses fell to negative values, necessitating a change to the trial protocol. After a third dose there was a suggestion of efficacy from 7-30 days but there is no data beyond 30 days to see how quickly this will wane.
C. Potential harms of COVID-19 vaccines for children
There has been great concern about myocarditis in adolescents and young adults, especially in males after the second dose, estimated at one per 2,600 in active post-marketing surveillance in Hong Kong. The emerging evidence of persistent cardiac abnormalities in adolescents with post-mRNA vaccine myopericarditis, as demonstrated by cardiac MRI at 3-8 months follow-up, suggests this is far from ‘mild and short-lived’. The potential for longer-term effects requires further study and calls for the strictest application of the precautionary principle in respect of the youngest and most vulnerable children.
Although post-vaccination myocarditis appears to be less common in 5-11-year-olds than in older children, it is, nonetheless, increased over baseline.
In the Pfizer study, 50% of vaccinated children had systemic adverse events, including irritability and fever. Diagnosis of myocarditis is much more difficult in younger children. No troponin levels or ECG studies were documented. Even a vaccinated child in the trial, hospitalized with fever, calf pain and a raised CPK, had no report of D-dimers, anti-platelet antibodies or troponin levels.
In Pfizer’s 5-11s post-authorization conditions, it is required to conduct studies looking for myocarditis and is not due to report results until 2027.
Of equal concern are, as yet unknown, negative effects on the immune system. In the 0-4s trial, only seven children were described as having “severe” COVID-19 – six vaccinated and one given placebo. Similarly, for the 12 children with recurrent episodes of infection, 10 were vaccinated against only two who received placebo. These are all tiny figures and much too small to rule out any adverse impacts such as antibody-dependent enhancement (ADE) and other impacts on the immune system.
Also unanswered is the question of Original Antigenic Sin. It is of note that in a large Israeli study, those infected after vaccination had poorer cover than those vaccinated after infection. In the Moderna trial, N-antibodies were seen in only 40% of those infected after vaccination, compared with 93% of those infected after placebo.
There is evidence of vaccine-induced disruption of both innate and adaptive immune responses. The possibility of developing an impaired immune function would be disastrous for children, who have the most competent innate immunity, which by now has been effectively trained by the circulating virus.
The unknown is whether there will be any adverse effect on T-cell function leading to an increase in cancers.
Also, in terms of reproductive function, limited animal bio-distribution studies showed lipid nanoparticles concentrate in ovaries and testes. Adult sperm donors have shown a reduction in sperm counts particularly of motile sperm, falling by three months post-vaccination and remaining depressed at four to five months.
Even for adults, concerns are rising that serious adverse events are more than hospitalizations from COVID-19.
D. Informed consent
For 5-11s, the JCVI, in recommending a “non-urgent offer” of vaccination, specifically noted the importance of fully informed consent with no coercion.
The complete omission of information explaining to the public the different and novel technology used in COVID-19 vaccines compared to standard vaccines, and the failure to inform of the lack of any long-term safety data, borders on misinformation.
E. Effect on public confidence
Vaccines against much more serious diseases, such as polio and measles, need to be prioritized. Pushing an unnecessary and novel, gene-based vaccine onto young children risks seriously undermining parental confidence in the whole immunization program.
The poor quality of the data presented by Pfizer risks bringing the pharmaceutical industry into disrepute and the regulators if this product is authorized.
In summary, young healthy children are at minimal risk from COVID-19, especially since the arrival of the Omicron variant. Most have been repeatedly exposed to SARS-CoV-2 virus, yet have remained well, or have had short, mild illness. As detailed above, the vaccines are of brief efficacy, have known short- to medium-term risks and unknown long-term safety. Data for clinically useful efficacy in small children are scant or absent. In older children, for whom the vaccines are already licensed, they have been promoted via ethically dubious schemes to the potential detriment of other, and vital, parts of the childhood vaccination program.
For a tiny minority of children for whom the potential for benefit clearly and unequivocally outweighed the potential for harm, vaccination could have been facilitated by restrictive licenses. Whether following the precautionary principle or the instruction to First Do No Harm, such vaccines have no place in a routine childhood immunization program.
Professor Angus Dalgleish, MD, FRCP, FRACP, FRCPath, FMed Sci, Principal, Institute for Cancer Vaccines & Immunotherapy (ICVI) Professor Anthony Fryer, PhD, FRCPath, Professor of Clinical Biochemistry, Keele University Professor David Livermore, BSc, PhD, Retired Professor of Medical Microbiology, UEA Professor John Fairclough FRCS FFSEM retired Honorary Consultant Surgeon Lord Moonie, MBChB, MRCPsych, MFCM, MSc, House of Lords, former Parliamentary Under-Secretary of State 2001-2003, formerCconsultant in Public Health Medicine Dr Abby Astle, MA(Cantab), MBBChir, GP Principal, GP Trainer, GP Examiner Dr Michael D Bell, MBChB, MRCGP, retired General Practitioner Dr Alan Black, MBBS, MSc, DipPharmMed, Retired Pharmaceutical Physician Dr David Bramble, MBChB, MRCPsych, MD, Consultant Psychiatrist Dr Emma Brierly, MBBS, MRCGP, General Practitioner Dr David Cartland, MBChB, BMedSci, General practitioner Dr Peter Chan, BM, MRCS, MRCGP, NLP, General Practitioner, Functional medicine practitioner Michael Cockayne, MSc, PGDip, SCPHNOH, BA, RN, Occupational Health Practitioner Julie Coffey, MBChB, General Practitioner John Collis, RN, Specialist Nurse Practitioner, retired Mr Ian F Comaish, MA, BM BCh, FRCOphth, FRANZCO, Consultant Ophthalmologist James Cook, NHS Registered Nurse, Bachelor of Nursing (Hons), Master of Public Health Dr Clare Craig, BMBCh, FRCPath, Pathologist Dr David Critchley, BSc, PhD in Pharmacology, 32 years experience in Pharmaceutical R&D Dr Jonathan Engler, MBChB, LLB (Hons), DipPharmMedDr Elizabeth Evans, MA (Cantab), MBBS, DRCOG, Retired Doctor Dr John Flack, BPharm, PhD, retired Director of Safety Evaluation at Beecham Pharmaceuticals and retired Senior Vice-president for Drug Discovery SmithKline Beecham Dr Simon Fox, BSc, BMBCh, FRCP, Consultant in Infectious Diseases and Internal Medicine Dr Ali Haggett, Mental health community work, 3rd sector, former lecturer in the history of medicine David Halpin, MB BS FRCS, Orthopaedic and trauma surgeon (retired) Dr Renée Hoenderkampf, General Practitioner Dr Andrew Isaac, MB BCh, Physician, retired Dr Steve James, Consultant Intensive Care Dr Keith Johnson, BA, DPhil (Oxon), IP Consultant for Diagnostic Testing Dr Rosamond Jones, MBBS, MD, FRCPCH, retired consultant paediatrician Dr Tanya Klymenko, PhD, FHEA, FIBMS, Senior Lecturer in Biomedical Sciences Dr Charles Lane, MA, DPhil, Molecular Biologist Dr Branko Latinkic, BSc, PhD, Molecular Biologist Dr Felicity Lillingstone, IMD DHS PhD ANP, Doctor, Urgent Care, Research Fellow Dr Theresa Lawrie, MBBCh, PhD, Director, Evidence-Based Medicine Consultancy Ltd, Bath Katherine MacGilchrist, BSc (Hons), MSc, CEO/Systematic Review Director, Epidemica Ltd. Dr Geoffrey Maidment, MBBS, MD, FRCP, Consultant Physician, retired Ahmad K Malik FRCS (Tr & Orth) Dip Med Sport, Consultant Trauma & Orthopaedic Surgeon Dr Kulvinder Singh Manik, MBBS, General Practitioner Dr Fiona Martindale, MBChB, MRCGP, General Practitioner Dr S McBride, BSc (Hons) Medical Microbiology & Immunobiology, MBBCh BAO, MSc in Clinical Gerontology, MRCP(UK), FRCEM, FRCP (Edinburgh). NHS Emergency Medicine & Geriatrics Mr Ian McDermott, MBBS, MS, FRCS(Tr&Orth), FFSEM(UK), Consultant Orthopaedic Surgeon Dr Franziska Meuschel, MD, ND, PhD, LFHom, BSEM, Nutritional, Environmental and Integrated Medicine Dr Scott Mitchell, MBChB, MRCS, Emergency Medicine Physician Dr Alan Mordue, MBChB, FFPH. Retired Consultant in Public Health Medicine & Epidemiology Dr David Morris, MBChB, MRCP(UK), General Practitioner Margaret Moss, MA (Cantab), CBiol, MRSB, Director, The Nutrition and Allergy Clinic, Cheshire Dr Alice Murkies, MD FRACGP MBBS, General Practitioner Dr Greta Mushet, MBChB, MRCPsych, retired Consultant Psychiatrist in Psychotherapy Dr Sarah Myhill, MBBS, retired GP and Naturopathic Physician Dr Rachel Nicholl, PhD, Medical researcher Dr Christina Peers, MBBS, DRCOG, DFSRH, FFSRH, Menopause specialist Rev Dr William J U Philip MB ChB, MRCP, BD, Senior Minister The Tron Church, Glasgow, formerly physician specialising in cardiology Dr Angharad Powell, MBChB, BSc (hons), DFRSH, DCP (Ireland), DRCOG, DipOccMed, MRCGP, General Practitioner Dr Gerry Quinn, PhD. Postdoctoral researcher in microbiology and immunology Dr Johanna Reilly, MBBS, General Practitioner Jessica Righart, MSc, MIBMS, Senior Critical Care Scientist Mr Angus Robertson, BSc, MB ChB, FRCSEd (Tr & Orth), Consultant Orthopaedic Surgeon Dr Jessica Robinson, BSc(Hons), MBBS, MRCPsych, MFHom, Psychiatrist and Integrative Medicine Doctor Dr Jon Rogers, MB ChB (Bristol), Retired General Practitioner Mr James Royle, MBChB, FRCS, MMedEd, Colorectal surgeon Dr Roland Salmon, MB BS, MRCGP, FFPH, Former Director, Communicable Disease Surveillance Centre Wales Sorrel Scott, Grad Dip Phys, Specialist Physiotherapist in Neurology, 30 years in NHS Dr Rohaan Seth, BSc (hons), MBChB (hons), MRCGP, Retired General Practitioner Dr Gary Sidley, retired NHS Consultant Clinical Psychologist Dr Annabel Smart, MBBS, retired General Practitioner Natalie Stephenson, BSc (Hons) Paediatric Audiologist Dr Zenobia Storah,MA (Oxon), Dip Psych, DClinPsy, Senior Clinical Psychologist (Child and Adolescent) Dr Julian Tompkinson, MBChB MRCGP, General Practitioner GP trainer PCME Dr Noel Thomas, MA, MBChB, DCH, DObsRCOG, DTM&H, MFHom, retired doctor Dr Stephen Ting, MB CHB, MRCP, PhD, Consultant Physician Dr Livia Tossici-Bolt, PhD, Clinical Scientist Dr Carmen Wheatley, DPhil, Orthomolecular Oncology Dr Helen Westwood MBChB MRCGP DCH DRCOG, General Practitioner Mr Lasantha Wijesinghe, FRCS, Consultant Vascular Surgeon Dr Damian Wilde, PhD, (Chartered) Specialist Clinical Psychologist Dr Ruth Wilde, MB BCh, MRCEM, AFMCP, Integrative & Functional Medicine Doctor
Defending the Republic, a Texas-based non-profit filed a Freedom of Information Act lawsuit against the Food and Drug Administration for refusing to turn over records related to the approval of Moderna’s COVID-19 vaccines.
The group filed a Freedom of Information Act (FOIA) request seeking the production of records relating to the Food and Drug Administration’s (FDA) internal review process of Moderna’s COVID-19 vaccine marketed as “Spikevax.” Given that the forces impacting the FDA’s decision to authorize the vaccine could have influenced Americans’ decision on whether or not to get vaccinated against COVID-19, Defending the Republic requested expedited processing of relevant records.
“Please provide all data and information submitted by Moderna relating to the FDA review and approval of Spikevax. This includes, but is not limited to, all safety and effectiveness data and information; all data and information in the biological product file; and all ingredients,” outlined the initial FOIA request.
On February 9th, less than a week after the initial FOIA was filed, the FDA refused the request for expedited processing, prompting Defending the Republic to appeal the decision.
“The FDA declined the appeal, leaving Defending the Republic with no choice but to file this action seeking a court order requiring the FDA produce the requested records on an expedited schedule— just as those who obtained a court order for the expedited production of records relating to the FDA approved Pfizer-BioNTech vaccine,” explains a complaint filed by Defending the Republic.
Defending the Republic was especially interested in better understanding the review process for Moderna’s COVID-19 vaccine, as data has shown its risk were not adequately explained to those receiving it and data surrounding its efficacy remains obscured. As Defending the Republic explains:
Despite the FDA’s promises, a closer inspection of the Spikevax approval reveal there may be glaring issues in the approval process. The Spikevax package insert concedes “[a]vailable data on SPIKEVAX administered to pregnant women are insufficient to inform vaccine-associated risks in pregnancy.” And while the FDA publicly pronounced that the “data demonstrated that Spikevax was 93% effective in preventing COVID-19,” the Spikevax fact sheet for recipients and caregivers provides important context omitted by the public officials: “The [Spikevax] duration of protection against COVID19 is currently unknown.
The lawsuit comes amidst several National Pulse exposés revealing how lobbyists from pharmaceutical companies including Moderna have entrenched themselves within Washington, D.C.
Do You Have Shingles or HIV?
Pfizer & Friends Just Happen to Have the Solution for You
Greg Hunter: “So they are marketing to people with diseases that they knowingly caused?”
Dr. Ryan Cole: “In my opinion, yes.”
– A Moderna study confirms an uptick in shingles. What do these companies do? Create a shingles solution.
– Pfizer jab gets emergency use authorization for children. What do they do? Buy a heart treatment company.
“They knew in advance all these harms. You can look back at years of mRNA trials and animals and the reason we haven’t done this on a large scale before is because they never worked.
There were too many adverse effects over time to where it wasn’t safe enough to bring forward to humanity.”
MONKEYPOX FALSE FLAG
>Biden Crime Family to reap massive profits from monkeypox vaccines
As you might expect, the current White House occupant is about to rake in boatloads of cash from the new monkeypox “vaccines” that are currently under development.
The Penn Biden Center, a globalist think tank at the University of Pennsylvania Hospital, is receiving a flood of cash, we now know, to create the next wave of plandemic injections at warp speed. And as its name suggests, the Penn Biden Center is directly tied to the Biden Crime Family.
Patrick Howley told Owen Shroyer during a recent live transmission of “War Room” that the pharmaceutical-industrial complex is greasing the skids for the Biden Crime Family to profit heavily from the monkeypox false flag event that is now unfolding.
“The University of Pennsylvania, which hosts Joe Biden’s think tank the Penn Biden Center and paid Joe Biden in the lead-up to his run for president, got paid by the company Bavarian Nordic to perform a clinical trial on the Bavarian Nordic monkeypox vaccine,” stated an article by Howley that was published by National File.
“Joe Biden’s host university profited from helping Bavarian Nordic develop the MVA-BN monkeypox vaccine.”
Monkeypox is a coverup (distraction?) for covid “vaccine” adverse events, including AIDS
(Natural News) The media’s new obsession over monkeypox could be a planned diversion away from the many adverse effects that are now appearing in people who took Wuhan coronavirus (Covid-19) “vaccines.”
Suddenly the monkey disease is said to be spreading among the LGBT community, and the same type of fearmongering that appeared at the start of the Fauci Flu plandemic is once again being deployed by the government and the media. (Related: Bill Gates and other deep state criminals held a monkeypox “simulation” event last year that predicted the current outbreaks.)
Even though this is hardly the first time that monkeypox has jumped ship from animals to humans, it is all of a sudden a major deal, we are told. Could it be that this is all a coverup or distraction to keep people fixated on the next scare rather than all the health damage being caused by Operation Warp Speed injections?
“The new evolving hysteria surrounding the alleged emergence of ‘monkeypox’ in Western nations is not what it appears to be,” reports Exposé News (UK). “We are not witnessing the monkeypox virus run rampant across first world countries for the first time ever.”
“Instead, we are witnessing the latest attempt to advance Draconian biosecurity policies through a monumental coverup of the devastating damage done to the immune systems of people who have had the Covid-19 vaccine. Damage so severe that it can be likened to Acquired Immunodeficiency Syndrome.”
Will monkeypox become the next global plandemic?
It turns out that monkeypox is really not that big of a deal. It is much less contagious than coronaviruses and not nearly as big of a threat as smallpox, its biological relative.
Chances are that very few people will actually catch it, save for those involved in homosexual sexual activity. So why all the ballyhoo about monkeypox – and why now specifically?
While monkeypox has mostly been restricted to Africa throughout its history of circulation, it did escape the continent and arrive in the United States for the first time in 2003. Since then, there have been a few minor outbreaks.
Now we are being told that monkeypox is spreading like wildfire at LGBT festivals in Europe, and the same type of rhetoric used in early 2020 to scare the world about covid is once again being used to scare the world about monkeypox.
“The main points to take away from this are that the alleged monkeypox disease is extremely rare, has rarely been seen outside of Africa, and has never been recorded in multiple countries outside of Africa at the same time,” the Exposé explains.
“So with that being the case, do you not find it strange that we are suddenly being told that cases of monkeypox are now being recorded in the USA, Canada, the UK, Australia, Sweden, the Netherlands, Belgium, France, Spain, Italy and Germany, all at the same time?”
A map of all the places where monkeypox is suddenly an issue reveals that only those areas of the world where Wuhan coronavirus (Covid-19) jabs were introduced are reporting “cases” of it. Could it all be a big distraction from the elephant in the room known as Fauci Flu shot adverse events?
“… evidence suggests we’re not witnessing an outbreak of monkeypox across first-world countries at all,” reports indicate.
“Instead, we’re witnessing the consequences of the damage that has been caused to immune systems by the Covid-19 injections in the very same first-world countries, and authorities are rushing to cover it up.”
The longer time goes on, the more we are going to witness vaccine-induced AIDS (VAIDS) manifest in the “fully vaccinated.” With that said, monkeypox hysteria will likely continue until they move on to the next distraction.
Some people are expecting the Monkey Pox scam to play out exactly like COVID (with lockdowns and vaccine mandates for employment and venues. This is a mistake. The enemy has adjusted their strategy. Many will be caught off guard.
Instead of the general lockdowns and mandates we saw during covid, this time they will track and trace extensively; targeting individuals and their contacts with long quarantines and ring vaccination. The psychology used will be formidable and much more difficult to resist. Many who refused to comply in round one will fold.
Ring vaccination means that anyone caught up in their contact tracing will be detained by specially trained teams, isolated and pressured / forced to take the vaccine. In some countries force will be used early on, but even in jurisdictions where one is not legally obligated to comply the pressure that these teams apply will be extreme. The long quarantines will add an additional incentive to give in. When the only way to avoid extended house arrest (and eventually quarantine camps) is to accept the jab, compliance can be achieved without general mandates (though we may see these in some jurisdictions).
This targeting and isolation of individuals is nefarious for a number of reasons. While general mandates and lockdowns tend to evoke widespread outrage, they know people won’t take to the streets en masse if they aren’t personally affected at the moment. They intend to pick you off one at a time starting with the least resistant. This is why they are focused on the gay community in the opening act. The gay community is overwhelmingly left wing. Most of this demographic will accept the vaccine without hesitation as will the majority of those in their social circles. This will allow the enemy to work out the kinks in the system before addressing the trouble makers.
Some of you might be wondering how on earth they will be able to take this clown show to such extremes. After all, Monkey Pox is very mild and only lasts a few weeks. However, the narrative is already being cultivated that there is something unusual about this particular strain. It’s “spreading” faster than previous variants, and some of the symptoms are unusual. Those of you who have been paying attention know that this is a cover for the side effects of COVID-19 vaccination. There are a multitude of auto-immune skin issues showing up that look like pox, and with immune systems decimated, the vaccinated are experiencing a resurgence of latent viruses, with shingles being one of the most common symptoms. Since diagnosis comes down to a fraudulent PCR test, all of this can be attributed to Monkey Pox.
Here’s where it gets nasty. The long term side effects of the initial COVID jabs are just beginning to reveal themselves, and all cause mortality among the vaccinated is already becoming impossible to hide. What this means is that while COVID started as a bad flu and ended as a mild cold, Monkey Pox will made to look like it is evolving into something absolutely horrific. People will get sick and stay sick. Others will die suddenly. The fear this will generate (and the resulting mass psychosis) will make you miss the good old days of COVID.
The food and energy shortages that are kicking off at the same time are an important part of the equation. Not only will rationing give those in power far more more leverage, malnutrition and cold will also weaken the population physically and make them more susceptible to disease. Electricity and internet blackouts will make it much harder to organize resistance and will provide cover for the worst abuses.
For years we have warned people to get out of the cities. Now you know why. This is the final window for that move. There will be no fuel for vehicles soon (and you can only walk so far when you are starving).
This ends in war, but in war timing is everything. Let the cities burn in the distance. Let the enemy expend their ammunition and weaken their armies. Wait for the right moment.
These are the Uk, Eu and American reports. These are very frightening.
Unrelated to this VAERS report, Pfizer has also released more documents showing that they knew about the side effects before they released the vaccines.
They skipped phase 2 after the animal tests on phase one which killed all the animals.
They skipped to phase 3 which is supposed to be tested on several volunteers. However, they used the general public for phase 3 which they knew would have severe consequences. Our governments, FDA, WHO and the whole system knew about this and still, they are injecting children.
The deaths and injuries of these poor children are of no consequence to anyone involved. The public is put into a state of fear over Covid which does not exist.
It’s only when you are vaccinated that you become unwell and are tricked into believing you have covid and not the side effects of the vaccines.
This must stop!! The next pandemic will be monkeypox starting with the gay community. There is no monkeypox, but the fear will be put into the gay community and they will all go for the monkeypox vaccine which will give them monkeypox.
Professor Dolores Cahill’s research suggests that those vaccinated with an mRNA injection have between 3-5 years to live – even if they have had only one jab.
This is the most terrifying interview I’ve seen with Professor Dolores Cahill.
Everything that she has said over the last 2 years has been correct. I’ve heard this mentioned somewhere before, but to hear it from this Professor, sort of makes it hit home. I have 3 grown-up daughters who have had the jab, it’s frightening to know what I’ve just heard.
Click on the link below, there are other videos too.
Our enemies are obsessed with jamming our OODA Loops. They do not want us to have even a moment to think. An OODA loop is a decision making process: observe–orient–decide–act. We take in information, and we make a decision on how to act to change things. Our enemies keep distracting us with constantly changing information, and we keep getting stuck in the OO stage, never making decisions, never acting to change things, because we are constantly trying to figure out the nature of the trap we are caught in. But that is the trap we are caught in! We end up stuck in endless puzzling debates, making no productive plans to achieve victory in even one small way.
When a fresh news story gets hyped up, and people say “oh oh they are just distracting us”, it is THINKING TIME they are distracting us from. A moment for the dust to settle, for even a minute of propaganda-free time, to be able to make a plan to counter our enemy’s plans. They cannot allow us this minute. We are allowed no firm place to stand. They have to bombard us with useless factoids and storylines 24/7, little rabbit holes and dead-ends and intrigue and drama, or else we might form together into something capable of defeating their psychological operations. Distraction and overload is their primary weapon against us. Unfortunately, we keep falling for this trick.
The OODA loop is the cycle observe–orient–decide–act, developed by military strategist and United States Air Force Colonel John Boyd. Boyd applied the concept to the combat operations process, often at the operational level during military campaigns. It is now also often applied to understand commercial operations and learning processes. The approach explains how agility can overcome raw power in dealing with human opponents. It is especially applicable to cyber security and cyberwarfare.
The OODA loop has become an important concept in litigation, business,law enforcement, and military strategy. According to Boyd, decision-making occurs in a recurring cycle of observe–orient–decide–act. An entity (whether an individual or an organization) that can process this cycle quickly, observing and reacting to unfolding events more rapidly than an opponent, can thereby “get inside” the opponent’s decision cycle and gain the advantage.