13 reasons why you should not allow your child to get the Covid-19 Vaccine

13 reasons why you should not allow your child to get the Covid-19 Vaccine

At a press conference on Monday September 13th, the four Chief Medical Officer’s (CMO’s) of the United Kingdom advised the UK Government to offer the Pfizer vaccine to children aged between 12 and 15.

Around 3 million under-16s are due to be offered the jabs after Chris Whitty endorsed the move, claiming it may “help prevent outbreaks in classrooms and further disruptions to education this winter”.

Doses will be largely administered through the existing school vaccination programme and parental consent will be sought. But children will be able to overrule their parents’ decision in the case of a conflict if they are deemed mature and competent enough, which has rightly caused fury.

For a child to be competent enough to make the decision to have the vaccine they should be made aware of all the facts before they reach their decision, and the same can be said for parents who wish to consent to their child having the jab. So we’ve compiled 13 factual reasons why you should not allow your child to get the Covid-19 vaccine…

Reason No. 1
86% of Children suffered an Adverse Reaction to the Pfizer Covid-19 Vaccine in the Clinical Trial

The information is publicly available and contained within a US Food & Drug Administration (FDA) fact sheet which can be viewed here (see page 25, table 5 on-wards).

That fact sheet contains two tables that detail the alarming rate of side effects and damage experienced by 12 – 15- year-old children who were given at least one dose of the Pfizer mRNA injection.

The tables shows that 1,127 children were given one dose of the mRNA jab, but only 1,097 children received the second dose. This fact in itself raises questions as to why 30 children did not receive a second dose of the Pfizer jab.

Of the 1,127 children who received a first dose of the jab 86% experienced an adverse reaction. Of the 1,097 children who received a second dose of the jab 78.9% experienced an adverse reaction.

Reason No. 2
1 in 9 Children suffered a Severe Adverse Reaction leaving them unable to perform daily activities in the Pfizer Clinical Trial

For children 12 to 15 years of age, the Pfizer Covid-19 vaccine clinical trial found the overall incidence of severe adverse events which left them unable to perform daily activities, during the two-month observation period to be 10.7%, or 1 in 9, in the vaccinated group and 1.9% in the unvaccinated group.

Consequently, children who received the vaccine had nearly six times the risk of a severe adverse event occurring in the two-month observation period compared to children who did not receive the vaccine. In addition, the incidence of Covid-19 in the unvaccinated group was 1.6%, therefore, there were almost seven times more severe adverse events observed in the vaccinated group than there were Covid-19 cases in the unvaccinated group.

This information is all freely available to see in official Food and Drug Administration (FDA) documents and official Centre for Disease Control (CDC) documents.

Reason No. 3
Just 9 deaths associated with Covid-19 have occurred in Children since March 2020

Official NHS data which can be viewed here (see Table 3 – COVID-19 deaths by age group and pre-existing condition of the downloadable excel document) shows that since March 2020 just 9 people under the age of 19 have died with Covid-19 who had no known pre-existing conditions in England’s hospitals, up to the 26th August 2021. The data also shows that just 39 people under the age of 19 have died with Covid-19 in the same time frame who did have other serious underlying conditions.

There are approximately 15.6 million people aged 19 and under in the United Kingdom which means just 1 in every 410,526 children and teenagers have allegedly died with Covid-19 in 18 months who had other serious pre-existing conditions. Whilst just 1 in every 1.7 million children have allegedly died with Covid-19 in 18 months, who had no know pre-existing conditions.

A scientific study titled ‘Deaths in Children and Young People in England following SARS-CoV-2 infection during the first pandemic year: a national study using linked mandatory child death reporting data’ (which can be found here), conducted by Clare Smith of NHS England and Improvement and several Universities also concluded that children are at negligible risk of death, hospitalisation, or serious illness due to the alleged Covid-19 virus.

The study collated data from the National Child Mortality Database; a mandatory system that records all deaths in Children under 18 years of age in England. What the researchers found is that just 25 children under the age of 18 died of Covid-19 between March 2020 and February 2021, with 15 of the 25 having a pre-existing life-limiting condition, and 19 of the 25 having a chronic condition.

The study also found that 16 of the 25 children who sadly died had two or more comorbidities with 8 children suffering pre-existing neurological and respiratory problems, 3 children suffering pre-existing neurological and cardiology problems, and 3 children suffering respiratory and cardiology problems.

Reason No. 4
The risk of Children developing serious illness due to Covid-19 is extremely low

A study (found here) led by Professor Russell Viner of UCL Great Ormond Street Institute of Child Health, published on the medRxiv server, found that 251 young people aged under 18 in England were admitted to intensive care with Covid-19 during the first year of the pandemic (until the end of February 2021).  

The results of the study found that there were 5,830 admissions associated with Covid-19 among children up to 17 years of age during the pandemic year, this represents just 1.3% of secondary care admissions among children.

The lead author of the study said: “These new studies show that the risks of severe illness or death from SARS-CoV-2 are extremely low in children and young people”.

Reason No. 5
The Pfizer Covid-19 Vaccine is experimental and still in Clinical Trials

The Pfizer mRNA Covid-19 injection is in fact only temporarily authorised (see official MHRA document here) for emergency use only. In October the government made changes to the Human Medicines Regulations 2012 to allow the MHRA to grant temporary authorisation of a Covid-19 vaccine without needing to wait for the EMA.

A temporary use authorisation is valid for one year only and requires the pharmaceutical companies to complete specific obligations, such as ongoing or new studies. Once comprehensive data on the product have been obtained, standard marketing authorisation can be granted. This means that the manufacturer of the vaccine cannot be held liable for any injury or death that occurs due to their vaccine, unless it was due to a quality control issue.

The reason the Pfizer mRNA Covid-19 injection has only been granted temporary authorisation is because it is still in clinical trials that are not set to conclude until May 2nd 2023. You can see the official Clinical Trial Study Tracker for the Pfizer jab on the US National Library of Medicine site here.

This is the first time mRNA injections have ever been authorised for use in humans (see here), and the long term side effects are not known, meaning the millions of people around the world who have had the Pfizer Covid-19 injection are essentially taking part in an experiment.

Reason No. 6
Three Scientific Studies conducted by the UK Government, Oxford University, & CDC, which were published in August have found the Covid-19 Vaccines do not work

New research in multiple settings shows that the alleged Delta Covid-19 variant, the now dominant variant in the UK, produces very high viral loads which are just as high in the vaccinated population compared to the unvaccinated population. Therefore, vaccinating individuals does not stop or even slow the spread of the alleged dominant Delta Covid-19 variant.

CDC Study

The CDC study (found here) focused on 469 cases among Massachusetts residents who attended indoor and outdoor public gatherings over a two week period. The results found that 346 of the cases were among vaccinated residents with 74% of them presenting with alleged Covid-19 symptoms, and 1.2% being hospitalised. However, the remaining 123 cases were among the unvaccinated population with just 1 person being hospitalised (0.8%).

Oxford University Study

The Oxford University study (found hereexamined 900 hospital staff members in Vietnam who had been vaccinated with the Oxford / AstraZeneca viral vector injection between March and April 2021. The entire hospital staff tested negative for the Covid-19 virus in mid May 2021 however, the first case among the vaccinated staff members was discovered on June 11th.

All 900 hospital staff were then retested for the Covid-19 virus and 52 additional cases were identified immediately, forcing the hospital into lockdown. Over the next two weeks, 16 additional cases were identified.

The study found that 76% of the Covid-19 positive staff developed respiratory symptoms, with 3 staff members developing pneumonia and one staff member requiring three days of oxygen therapy. Peak viral loads among the fully vaccinated infected group were found to be 251 times higher than peak viral loads found among the staff in March – April 2020 when they were not vaccinated.

UK Department of Health & Social Care Study

The UK Department of Health & Social Care study (found here) is an analysis of ongoing population wide SARS-CoV-2 monitoring in the UK and includes measures of viral load among the population.

The study found that viral loads among the vaccinated and unvaccinated population are virtually the same, and much higher than had been recorded prior to the Covid-19 injection roll-out. The study also found that the majority of cases among the vaccinated population were presenting with symptoms when they became positive.

The authors of the study conclude that the Pfizer and Oxford / AstraZeneca injection have lost efficacy against what they claim to be the Delta Covid-19 variant.

Reason No. 7
Public Health England Data shows the majority of Covid-19 Deaths are among the Vaccinated and suggests that the Vaccines worsen disease

A report titled ‘SARS-CoV-2 variants of concern and variants under investigation in England’ (found here – see Table 5 Page 21), is the 22nd technical briefing on alleged variants of concern in the United Kingdom published by Public Health England.

From February 1st 2021 up to August 29th 2021 nearly twice as many unvaccinated people account for confirmed cases of Covid-19 than those who are fully vaccinated.

However when you include the number to have received one dose of a Covid-19 injection the number of cases among the vaccinated group (222,693) actually surpasses the number that have been recorded among the unvaccinated population.

The total number of deaths to have occurred since February 2021 involving the Delta Covid-19 variant that have been linked to vaccination status total 1,698. Of these just 30% have been among the unvaccinated population, despite the fact most second vaccinations were administered between April and June.

Whereas the fully vaccinated account for 64.25% of Covid-19 deaths since February 2021, and when including the partly vaccinated in those numbers they account for 70%.

The data published by Public Health England actually suggests that the risk of death increases significantly in those who have been fully vaccinated.

536 deaths have occurred among 219,716 confirmed cases in the unvaccinated population since February. This is a case fatality rate of 0.2%. Whereas 1,091 deaths have occurred among 113,823 cases among the fully vaccinated population. This is a case fatality rate of 1%.

This means the Covid-19 injections seem to be increasing the risk of death due to Covid-19 by 400% rather than reducing the risk of death by 95% as claimed by the vaccine manufacturers, Public Health bodies, and the Government.

Reason No. 8
There have been at least 1.18 million Adverse Reactions to the Covid-19 Vaccines in the UK alone

The thirty-second report highlighting adverse reactions to the Pfizer / BioNTech, Oxford / AstraZeneca, and Moderna Covid-19 injections that have been reported to the UK Medicine Regulator’s (MHRA) Yellow Card scheme reveals that there have been 1,186,844 adverse reactions reported since the 9th December 2020 up to the 1st September 2021.

The reports for each available vaccine can be found here under the analysis print section and include adverse reactions such as blindness, seizure, stroke, paralysis, cardiac arrest and many other serious ailments.

The Pfizer mRNA injections has left at least 107 people fully paralysed and a number of other people partly paralysed up to the 1st September 2021. However, the MHRA state that an estimated 10% of adverse reactions are actually reported to the Yellow Card scheme, meaning the true figure of adverse reactions is immensely higher.

Reason No. 9
There have been more deaths in 8 months due to the Covid-19 Vaccines than there have been due to all other available Vaccines since the year 2001

The UK Medicine Regulator responded to a Freedom of Information (found here) request demanding to know how many deaths have occurred in the past 20 years due to all vaccines, and their response revealed that there have been four times as many deaths in just eight months due to the Covid-19 injections.

The request was made via email to the Medicine and Healthcare product Regulatory Agency (MHRA) on the 6th August 2021, and in answer to the question asked on the number of deaths due to all other vaccines in the past twenty years, the MHRA revealed that they had received a total of 404 reported adverse reactions to all available vaccines (excluding the Covid-19 injections) associated with a fatal outcome between the 1st January 2001 and the 25th August 2021 – a time frame of 20 years and 8 months.

However, according to the MHRA Yellow Card Report (see here – under each analysis print section) there have been 1,632 deaths reported as adverse reactions to the Covid-19 vaccines from December 9th 2020 up to September 1st 2021. This includes 16 deaths due to the Moderna jab, 24 deaths where the brand of vaccine was unspecified, 1,064 deaths due to the AstraZeneca vaccine, and 524 deaths due to the Pfizer mRNA injection.

Reason No. 10
The risk of Myocarditis (Heart Inflammation) in Children due to the Pfizer Vaccine

Myocarditis is inflammation of the heart muscle, whilst Pericarditis is inflammation of the protective sacs surrounding the heart. Both are serious conditions due to the fact the heart muscle cannot regenerate, and both conditions have officially been added to the safety labels of the Pfizer jab and Moderna jab by the MHRA (see here).

Myocarditis and pericarditis happen very rarely in the general (unvaccinated) population, and it is estimated that in the UK there are about 6 new cases of myocarditis per 100,000 patients per year and about 10 new cases of pericarditis per 100,000 patients per year.

The MHRA has undertaken a thorough review of both UK and international reports of myocarditis and pericarditis following vaccination against Covid-19 due to a recent increase in reporting of these events in particular with the Pfizer/BioNTech and Moderna vaccines, with a consistent pattern of cases occurring more frequently in young males.

Scientific Study published on the JAMA network, has also found that the incidence of myocarditis among vaccinated individuals is at least double what Health Authorities are claiming.

The new JAMA study (found here) showed a similar pattern to a CDC study (found here), although at higher incidence of myocarditis and pericarditis after vaccination, suggesting vaccine adverse event under-reporting.

The researchers calculated the average monthly number of cases of myocarditis or pericarditis during the pre-vaccine period of January 2019 through January 2021 was 16.9 compared with 27.3 during the vaccine period of February through May 2021.
The mean numbers of pericarditis cases during the same periods were 49.1 and 78.8.

Dr. George Diaz who conducted the study told Medscape that “Our study resulted in higher numbers of cases probably because we searched the EMR, and [also because] VAERS requires doctors to report suspected cases voluntarily,” Diaz told Medscape. Also, in the governments’ statistics, pericarditis and myocarditis were “lumped together”.

Reason No. 11
Children have died and are dying due to the Covid-19 Vaccines

The US Vaccine Adverse Event Reporting System (VAERS), which can be searched here by inputting the specific VAERS ID shows that several children have died in the US after having the Covid-19 vaccine, with many suffering cardiac arrest.

A 16 year-old female received the Pfizer vaccine on the 19th March 2021. Nine days later the same female went into cardiac arrest at home. By the 30th March 2021 she had sadly died. Found under VAERS ID 1225942.

A 15 year-old female suffered cardiac arrest and ended up in intensive care four days after having the Moderna mRNA jab. She also sadly died. Found under VAERS ID 1187918.

Another 15 year-old female received her second dose of the Pfizer jab on the 6th June 2021. Sadly one day later she died suddenly without reason. Found under VAERS ID 1383620.

A 15 year-old male die due to an unexplained reason twenty-three days after having the Pfizer jab. Found under VAERS ID 1382906.

The above are sadly just a few examples of the deaths to have occurred among children due to the Covid-19 vaccines in the USA.

Reason No. 12
Who profits from your Child getting the Covid-19 Vaccine?

It may surprise you to know that GP’s were already being incentivised to inject the adult population with the Covid-19 vaccine with a payment of £12.58 for every dose administered.

So it may surprise you further to know that GP’s are being offered an additional payment of £10 on top of the £12.58 already offered for every injection administered to a child in the United Kingdom. All of this is documented in an official NHS document found here.

According to the last count made in 2020 there are approximately 3,154,459 children between the ages of 12 and 15 in the United Kingdom. Therefore GP’s across the UK could stand to make a combined £142.45 million if every child is injected with a Covid-19 vaccine.

A Freedom of Information request (found here) which the MHRA responded to in May 2021 revealed that the current level of grant funding received from the Bill & Melinda Gates Foundation amounts to $3 million and covers “a number of projects”. The MHRA being the UK Medicine Regulator to have granted emergency use authorisation for the Pfizer / BioNTech mRNA vaccine to be given to children.

Coincidentally, the Bill & Melinda Gates Foundation bought shares in Pfizer back in 2002 (see here), and back in September 2020 Bill Gates ensured the value of his shares went up by announcing to the mainstream media in a CNBC interview that he viewed the Pfizer jab as the leader in the Covid-19 vaccine race.

“The only vaccine that, if everything went perfectly, might seek the emergency use license by the end of October, would be Pfizer.”

The Bill & Melinda Gates Foundation also coincidentally bought $55 million worth of shares in BioNTech (see here) in September 2019, just before the alleged Covid-19 pandemic struck.

Can we really trust the MHRA to remain impartial when its primary funder is the Bill & Melinda Gates Foundation, who also own shares in Pfizer and BioNTech?

Reason No. 13
The Joint Committee on Vaccination & Immunisation have refused to recommend the Pfizer Vaccine be offered to Children

On the 3rd September 2021 the Joint Committee on Vaccination and Immunisation (JCVI) announced (see here) they were not recommending the Pfizer Covid-19 injection be offered to all children over the age of 12.

The assessment by the Joint Committee on Vaccination and Immunisation (JCVI) is that the health benefits from vaccination are marginally greater than the potential known harms. However, the margin of benefit is considered too small to support universal vaccination of healthy 12 to 15 year olds at this time.

The JCVI cited the following –

“For the vast majority of children, SARS-CoV-2 infection is asymptomatic or mildly symptomatic and will resolve without treatment. Of the very few children aged 12 to 15 years who require hospitalisation, the majority have underlying health conditions.”

Since 1st April 2009 the Health Protection (Vaccination) Regulations 2009 place a duty on the Secretary of State for Health in England to ensure, so far as is reasonably practicable, that the recommendations of JCVI are implemented (See here – page 6).

Yet in an unprecedented move, the Secretary for Health and the Government decided to bypass the JCVI and seek the advice of the four Chief Medical Officers (CMO’s) of the United Kingdom.

In their letter to the Government (found here), the UK CMO’s state they looked at wider public health benefits and risks of universal vaccination in this age group to determine if this shifts the risk-benefit either way. They claim in their letter that “the most important in this age group was impact on education”.

This raises some serious questions –

  1. Did Covid-19 close the schools? The answer is of course no. Schools were closed because of Government policy.
  2. Should a person take a medical treatment so that they are able to partake in society or education? The answer is couse no. A person should only ever take a medical treatment for a medical reason, in the case of the Covid-19 vaccine that reason should be to prevent infection; which it does not do, or prevent illness; which it will not do as children are at such low risk of suffering serious illness due to Covid-19.

The decision by Chris Whitty and his fellow Chief Medical Officers to advise the Government that the Covid-19 vaccines should be offered to children is not a decision based on science, it is instead a decision based on politics.

But we have just presented 13 factual reasons why you should not allow your child to get the Covid-19 vaccine, and each and every one is based on the science.

Now the choice is yours, or perhaps that of your child, we hope you make the correct one.

To view the original article, please visit >> https://theexpose.uk/2021/09/14/13-reasons-why-you-should-not-allow-your-child-to-get-the-covid-19-vaccine/

The Rationale for the Continued Vaccine Roll-Out is Not Evident

The Rationale for the Continued Vaccine Roll-Out is Not Evident

Friday, 30th July 2021

We appear to have serious problems with the Covid-19 vaccination programme. The evidence underpinning the claimed efficacy and safety of the Pfizer BNT162b2 vaccine is highly questionable. Statistical analysis raises numerous issues, and until these are addressed, the alleged benefits cannot be shown to outweigh the risks. 

With wider concerns expressed by some of the world’s leading immunologists, virologists and epidemiologists, justification for the continued vaccination programme appears to be lacking. Possible unacceptable risk is evident in every nation which has vaccinated a significant proportion of its population.

The vaccines appear to increase the mortality risk from Covid-19, something the authorities and the regulatory agencies have so far shown little or no interest in investigating.

Some of what we are about to discuss is necessarily speculative. It is based upon a full statistical analysis—but, absent a comprehensive investigation, we cannot be certain why this analysis appears to show an increased Covid-19 mortality risk following vaccination.

Equally, refusal to investigate this correlation is untenable. No claim of either vaccine safety or efficacy is justified without properly accounting for this statistical analysis.

Concerning Data Emerges in Israel

Recently, the UK Column interviewed, among others, Dr Hervé Seligmann (Part 1 here). Dr Seligmann has a B.Sc. in Biology from the Hebrew University of Jerusalem. He earned an M.Sc. in 1991 and gained his Ph.D in 2003. He has had over 100 scientific papers published. He works at the Emerging Infectious and Tropical Diseases Research Unit, Faculty of Medicine, Aix-Marseille University, Marseilles, France. His statistical research partner is the engineer Haim Yativ.

Dr Seligmann and Mr Yativ have posted an informative English-language resource page where you can see recent updates to their research. Their analysis of Israeli data appears to show a significant increased risk of Covid-19 mortality (for the vaccinated) during the period between receipt of the first and second vaccine doses, and for a brief period following the second dose. Their research has focused upon the Pfizer/BioNTech BNT162b2 vaccine (tozinameran).

Their research impacts the risk/benefit analysis for the Pfizer BioNTech mRNA vaccine. It brings the claims made about its efficacy and safety into considerable doubt. Their analysis should be assessed in light of the absence of completed clinical trials for the BNT162b2 vaccine, which are still in the recruitment phase.

Nor are there any completed clinical trials for any of the other leading vaccines used in western nations. AstraZeneca’s AZD1222 (or ChAdOx1-S) trial (NCT04516746) is due to be completed in February 2023. Moderna’s mRNA vaccine phase III trial (NCT04470427) should be concluded by October 2022. Johnson & Johnson’s Janssen trial (NCT04614948) is expected to near completion in May 2023.

There are no posted results for any of these trials. The vaccines have all been approved for population use under emergency authorisation for this reason. They are unlicensed medications and do not have marketing authorisation. The approval decision was made based solely on data provided to the regulators by the manufacturers.

In Israel, on 11 February 2021, Ynet published an article in which they made the following claim:

Data from the Ministry of Health obtained by Ynet show the huge gap between the completely vaccinated and the unvaccinated. According to them, the effectiveness of the vaccine is higher than 90% in all age groups, both in preventing coronary heart disease and in preventing serious illness and death.

It is important to note that Ynet’s statement is based upon an analytical comparison made between the “completely vaccinated” and the “unvaccinated”. Further data from the Israeli Ministry of Health was then made available and was reported on 11 March by the German media outlet Correctiv.org. Dr Seligmann and Mr Yativ then reanalysed the original datasets and found clear discrepancies between the data and the reported “benefits” of the vaccines.

Key to this issue was that the claimed “benefits” were only measured from completion of the second dose, and took no account of the risks in the five-week period between and immediately following the first and second dose. Seligmann and Yativ referred to this window as the “period of vaccination”. We will use the abbreviation “PoV” for this period throughout the rest of this article.

Seligmann and Yativ analysed the data from the Israeli Ministry of Health (included in their report—linked above) and the data from Dagan et al., 2021. They continue to monitor the datasets but, as already stated, this analysis was for the period up to 11 March.

They calculated an unvaccinated person’s Covid-19 mortality baseline risk from data covering the 303-day period between 1 March 2020 and 20 December 2020, when the Israeli BNT162b2 vaccine rollout began. They analysed the percentage of cases and deaths for the two age groups in the Israeli data (those below and those above 60 years of age) published by the actuaries at the health insurance company Clalit.

Using this data, Seligmann and Yativ calculated the daily percentage chance of Covid-19 mortality for the respective, unvaccinated cohorts. For those under 60, it was 0.00000257% per day. For Israeli citizens over 60, it was 0.00022631% per day. The data released by the Israeli Ministry of Health, for various intervals in the PoV, were then compared to these unvaccinated baselines.

Between 0 and 13 days after the first dose of the Pfizer vaccine, the Covid-19 daily mortality risk for the over 60’s was 0.003303%. This was more than 14.5 times higher than for the unvaccinated. More than thirteen days following the first dose of vaccination, this risk increased to 0.005484% per day; a risk more than 24.2 times greater than among the unvaccinated. This increased further, for the first six days after the second dose, to 0.006076% — representing a 26.85-fold increased risk of Covid-19 mortality for the vaccinated.

In the second week following the second dose, the risk for the over-60s remained at 18.4 times higher for the vaccinated. This gradually reduced to 6.7 times worse than the unvaccinated at fourteen days following the second dose, and the excess risk continued to decrease over the the next few weeks. The data showed that there is a a PoV of approximately five weeks during which there is a significantly increased risk of dying from Covid-19 for the vaccinated over-60s.

A similar increased risk of Covid-19 mortality was seen in the data for the under-60s. In the first two weeks following the first dose, the risk was increased 23.86 times. This increased further to a 42.4-times elevated risk in the second week after the first dose. In the first week following the second dose, the data indicated a 94-fold increase in the daily Covid mortality risk for the vaccinated. For the period studied, there was no noted increased risk to the under-60s beyond the first week following the second dose.

The Missing "Benefit" of BNT162b2 Vaccination

Seligmann and Yativ’s statistical analysis clearly showed a significantly higher risk of Covid-19 mortality for the vaccinated during the PoV. They then noted that once the vaccine had taken full effect, the Covid-19 mortality risk for the vaccinated reduced below the risk for the unvaccinated. They found an apparent benefit from the vaccine once the PoV had ended.

Taking into account that the general population risk of Covid-19 mortality is so low, they were able to calculate how many days of full vaccine protection would be required to compensate for the significant increased daily mortality risk during the PoV.

For the over-60s, after the first dose, the BNT162b2 vaccine would have to provide nearly two years of full protection (690.62 days) to achieve any net benefit. Seligmann and Yativ stated:

Pooling both age classes, on average, in order to not lose more lives than gain lives due to vaccination, the protective effects of the vaccine, without costs associated with 3d [a third dose] and more shots, would have to be absolute and with no other vaccine-related but COVID19-unrelated deaths for a period of at least 658 days.

The researchers also noted a number of important caveats. For example, the age distribution and relative risk classes for the unvaccinated wasn’t clear in the Israeli data. This could be a compounding factor for their analysis, and they have requested clarification. They have yet to receive a response.

Their initial analysis did not take account of non Covid-19 mortality patterns. They also disregarded the fact that vaccine protection is not absolute. They went on to extrapolate their research to look at broader mortality patterns. This indicated even further reason for concern, especially among children, suggesting that the vaccinated pose a risk to the unvaccinated.

Seligmann and Yativ noted that the Israeli Ministry of Health and the co-authors of the Dagan, et al. paper had commercial conflicts of interest with Pfizer. However, sticking to the data presented in the Dagan, et al. paper, they noted an overall threefold increase on Covid-19 infection rates for the vaccinated during the five-week PoV.

We might add our own caveat at this point: a positive RT-PCR test is not evidence of a “case” of Covid-19. However, Seligmann’s calculations are based upon the government’s definition of a case.

In summation, Seligmann and Yativ have identified an elevated risk of both infection and subsequent Covid-19 mortality, during the PoV with BNT162b2. This is so marked that to justify it, the absolute protection conferred by the vaccine (an absolute protection which is known not to exist) would have to be prolonged (for many years—without any need of boosters or further vaccination). If this is not the case, then any net benefit from the vaccine is extremely unlikely.

Media reports from Israel would seem to admit that a net benefit does not exist. The New York Times recently reported:

Researchers estimated that the Pfizer shot was just 39 percent effective against preventing infection in the country in late June and early July, compared with 95 percent from January to early April.

The Daily Telegraph reports that BNT162b2 recipients are already being required to take a booster. Pfizer CEO Albert Bourla announced that Pfizer’s claimed efficacy drops to 84% within six months. Bourla stated that supposed “efficacy” against severe disease declines by 6% every two months. He alleges that this necessitates the booster.

If Seligmann and Yativ’s statistical analysis is correct, this strongly indicates that there is no possible Covid-19 health benefit for the BNT162b2 vaccine. Consequently, a “booster”—of something which appears to cause harm—would be irrational.

Corroboration from Others

Seligmann and Yativ’s findings have seemingly been corroborated by the research of Dr Steve Ohana and Dr Alexandra Henrion-Caude. They found a large spike in mortality among the 20-49 age group in Israel. They then compared this to other nations with a high vaccine coverage (taking the jurisdiction of England & Wales) and noted the same phenomenon. They concluded:

Surges in mortality among young people are very rare events, and are usually associated with wars […] The mortality peak among 20 to 49-year-olds in February-March 2021 is therefore unprecedented and indeed concerning […] Our additional observation supporting this possible link between vaccination and youth mortality is the fact that common patterns of excess mortality were also observed in England and Wales […] [T]he established link between the Pfizer vaccine and myocarditis/autoimmune diseases in young adults further lend a physiological support. Such accumulation of concern should, in our view, urgently prompt a pause in the vaccination campaign, until the reasons of the youth excess mortality observed in mass vaccination countries are clarified.

In addition, Peter Schirmacher, director of the Pathological Institute in Heidelberg, Germany, who advocates Covid-19 vaccination, has highlighted the need for immediate post-mortem examinations of the vaccinated. Schirmarcher carried out more than forty autopsies on people who died shortly after vaccination in Germany. He found that up to 40% of them died from cerebral vein thrombosis or autoimmune disease that could be attributable to the vaccines

There is even a suggested mechanism explaining how this increased mortality could be occurring. An autopsy of a recently vaccinated 86-year-old decedent found that the S-protein (spike protein), whose production is induced by the BNT162b2 vaccine, was found in almost every organ of the man’s body. This is contrary to the claims of the mRNA vaccine manufacturers, who maintain that the S-protein is only produced by and remains at the vaccine site.  

Doctors for Covid Ethics are among the many renowned scientists and physicians who have raised concerns about the S-protein produced by the body’s cells following an mRNA Covid jab. They state:

The first injection will induce the expression of spike protein, and the formation of specific antibodies to it. Re-vaccination will lead to a second round of spike protein production, including in endothelial cells. The antibodies, now already present, will bind to these spikes and will direct attack of the complement system to these cells. Neutrophil granulocytes, too, will be activated by antibodies bound to the endothelial cells. Vascular damage and leakage will ensue.

Not only is there statistical evidence suggesting cause for concern; there is physiological evidence that could account for the data. It is not known whether the apparent increased mortality is derived from this suggested mechanism—and that is the point. Without a proper investigation, no-one knows.

Reason for Concern in the UK

Currently in the UK, the MHRA Yellow Card scheme data suggests that more than 1,500 people may have died as a result of vaccination. In addition, the MHRA has stated that Yellow Card reports only represent 10% of total vaccine related mortality, suggesting a plausible 15,000 vaccine related deaths so far in the UK.

The MHRA now states that this under-reporting estimate should not be used for Covid-19 vaccines, because (they allege) awareness of their Yellow Card scheme for vaccine adverse drug reactions has somehow improved. They have offered no evidence to substantiate this claim.

We might ask what the point of the MHRA Yellow Card scheme is. On the one hand, the agency states that its purpose is to act as an “early warning system” for possible vaccine harm. Yet the MHRA also states:

The suspected ADRs described in this report are not interpreted as being proven side effects of COVID-19 vaccines.

This would be acceptable if the MHRA had investigated those possible adverse reactions to establish whether they were ADRs. Again, there is no evidence that they have. All we can say is that the MHRA does not interpret them as vaccine ADRs. Therefore, the chance of their Yellow Card scheme actually providing an “early warning” would appear to be nil.

If we apply Seligmann and Yativ’s analysis to the UK vaccine rollout data, a very worrying picture emerges. The Israeli researchers considered the BNT162b2 vaccine in Israel. This brand was also the first vaccine administered to the most vulnerable in the UK. It is not unreasonable, therefore, to apply their findings to the UK data.

The first dose of the BNT162b2 was given to Margaret Keenan on 8 December 2020. The vaccine rollout began in earnest between a week and two weeks later. As in Israel, it was in full swing by 20 December 2020.

Brian Pinker was the first person in the UK to receive an AstraZeneca vaccine, on 4 January 2021, nearly a month later. The rollout of the AstraZeneca vaccine also took a couple of weeks to get fully up to speed.

The vaccines were distributed in keeping with the UK Government’s priority schedule. This meant that the first to receive the vaccine were the most vulnerable in British care homes, hospitals and other care settings.

On 10 January 2021, the then Health Secretary, Matt Hancock, confirmed figures reporting that 2.3 million people had been vaccinated for Covid-19 in the UK. While specific data on the vaccine distribution has not been released, it is clear that the vast majority of these people must have received BNT162b2.

On 22 November 2020, the seven-day average for daily Covid-19 mortality in the UK stood at 466.4. By 8 December—the day of Keenan’s vaccination—the average had dropped to 428.9. This represented a decline of 8% in the daily mortality average in just over two weeks.

By 19 January 2021, the seven-day daily Covid-19 mortality average had increased by nearly 300% to 1285.7. Using Seligmann and Yativ’s PoV—assuming a full BNT162b2 vaccine programme from 15 December onward, and using the UK Government’s own statistics—it appears that a significant proportion of 29,755 reported Covid-19 deaths may have been attributable to the increased mortality risk presented by the vaccine.

We cannot say, without a thorough investigation, what that proportion is. However, the distribution of that mortality does appear to correlate strongly with the distribution suggested by Seligmann and Yativ’s analysis.

Therefore, it is reasonable to conclude that the Yellow Card data indicating a possible 1,500 vaccine-related deaths appears to underestimate vaccine harm considerably. The known phenomenon of under-reporting—combined with the remarkable correlation between the Israeli analysis, the vaccine rollout of BNT162b2 and the official UK Government statistics—suggests that the Pfizer vaccine is dangerous.

As the data currently stands, it seems that many thousands of alleged Covid-19 deaths may have occurred due to the additional risks posed by the BNT162b2 vaccine alone. Given the lack of clinical trials, it is not possible for anyone to state categorically that any of the major Covid-19 vaccines is either effective or safe; certainly not Pfizer BNT162b2. 

Government claims of lives saved do not stand up to scrutiny. When we also consider the growing evidence of risks associated with other vaccines, the rationale for the continued vaccine rollout is not evident.

To view the original article, please visit >> https://www.ukcolumn.org/article/the-rationale-for-the-continued-vaccine-roll-out-is-not-evident

Dr Peter McCullough reveals the Covid-19 Vaccines are Bioweapons and a CDC whistle-blower

Dr Peter McCullough reveals the Covid-19 Vaccines are Bioweapons and a CDC whistle-blower has confirmed 50,000 Americans have died due to the jabs

BY  ON 

The most highly cited physician on the early treatment of COVID-19 has come out with an explosive new interview that blows the lid off the medical establishment’s complicity in the unnecessary deaths of thousands.

Dr. Peter McCullough said these deaths have been facilitated by a false narrative bent on pushing an all-new, unproven vaccine for a disease that was highly treatable.

He said the alleged Covid-19 virus is a bioweapon and the vaccines represent “phase two” of that bioweapon.

“As this, in a sense, bioterrorism phase one was rolled out, it was really all about keeping the population in fear and in isolation and preparing them to accept the vaccine, which appears to be phase two of a bioterrorism operation,” McCullough said in a June 11 webinar with German attorney Reiner Fuellmich and several other doctors.

He noted:

“Both the respiratory virus and the vaccine delivered to the human body the spike protein, the gain of function target of this bioterrorism research.”

“Now I can’t come out and say all this on national TV today or at any time,” he continued. “But, what we had learned over time is that we could no longer communicate with government agencies. We actually couldn’t even communicate with our propagandised colleagues in major medical centres, all of which appear to be under a spell, almost as if they are hypnotized right now.”

He did not hold back in his criticism of his colleagues in the medical community.

“And doctors, good doctors, are doing unthinkable things, like injecting biologically active messenger RNA that produces this pathological spike protein into pregnant women. I think when the doctors wake up from their trance they’re going to be shocked to think what they’ve done to people.”

McCullough is professor of medicine and vice chief of internal medicine at Baylor University and also teaches at Texas A&M University. He is an epidemiologist, cardiologist and internist and has testified before the Texas State Senate related to COVID-19 treatments. He holds the distinction of being the most widely cited physician in the treatment of COVID-19 with more than 600 citations in the National Library of Medicine.

In the interview McCullough said:

“The first wave of the bioterrorism is a respiratory virus that spread across the world, and affected relatively few people—about one percent of many populations—but generated great fear.”

He said the virus targeted primarily people over 50 with multiple medical conditions. It poses almost no risk to children.

He said 85 percent of the more than 600,000 U.S. deaths could have been prevented with a multi-drug treatment given in the early to mid-point of the disease.

Instead, people were told to stay home and not return to the hospital unless their symptoms got worse, such as severe breathing problems. By then it was too late for many. They were placed on ventilators and died.

The vast majority of doctors jumped in lockstep to follow these erroneous “guidelines” handed down by the World Health Organisation and the U.S. Centre for Disease Control. Those guidelines neglected to place any focus on the treatment of sick patients and, from the beginning, as early as April 2020, started emphasizing the need for a vaccine as the only real hope of beating back the virus.

The federal Vaccine Adverse Event Reporting System [VAERS] logged 5,993 reports of deaths of people injected with the COVID vaccine between Dec. 14, 2020, and June 11, 2021. That’s more than all the deaths reported to VAERS from all other vaccines combined over the last 22 years.

But these numbers, as shocking as they are, don’t scratch the surface of the actual number of dead Americans, said McCullough.

“We have now a whistleblower inside the CMS, and we have two whistleblowers in the CDC. We think we have 50,000 dead Americans. Fifty thousand deaths. So we actually have more deaths due to the vaccine per day than certainly the viral illness by far. It’s basically propagandized bioterrorism by injection.

McCullough added that “every single thing that was done in public health in response to the pandemic made it worse.”

He said the suppression of early COVID treatments, such as hydroxychloroquine and especially Ivermectin, “was tightly linked to the development of a vaccine.”

Without the suppression of the already-available treatments, the government would not have been able to legally grant Emergency Use Authorisation to the three vaccines rushed to market in the USA by Moderna, Pfizer and Johnson and Johnson.

In the case of Moderna, the U.S. government is co-patent holder through the National Institutes of Health, a clear conflict of interest, and confidential documents reveal Moderna sent a coronavirus mRNA vaccine candidate was sent to a US University in December 2019, weeks before Covid-19 was allegedly known to even exist.

“I published basically the only two papers that teach doctors how to treat COVID-19 at home to prevent hospitalisation and death…If treated early, it results in an 85 percent reduction in hospitalisations and death,” McCullough said.

So not only were the vaccines rolled out unnecessarily by suppressing already available, effective treatments, but the FDA and CDC are now covering up tragic numbers of deaths caused by their experimental mRNA injections.

McCullough said he has organized groups around the world that emphasise early treatment.

“Governments have actually tried to block early treatment of Covid patients, so we created a home patient guide,” he said.

“We broke through to the people, and the people who got sick with COVID called in to get medications from mail-order distribution pharmacies. So without the government even knowing what went on, we crushed the epidemic here in the United States towards the end of December and January.

“We basically took care of the pandemic with about 500 doctors and telemedicine services. And to this day we treat about 25 percent of the US COVID-19 population that actually are at high risk, over age 50 with medical problems or present with severe symptoms. And we basically handled the pandemic, and at the same time we’ve tried to keep ourselves above the political fray.”

McCullough said his focus has recently turned to the unnecessary and dangerous injections.

“We are working to change the public view of the vaccine. The public initially accepted the vaccine and we had to kind of slowly turn the ship. Now, in the U.S. the rates of vaccination have been dropping since April 8. Most of the vaccination centres are empty.

“We have a lot going on in the United States. We are engaging more and more attorneys.

Source

COVID-19 Origins Revealed

COVID-19 Origins Revealed


By Mike Adams

June 8, 2021

The cover-up has imploded. Covid-19 was engineered in a lab, and the desperate attempts to hide its true origins are rapidly collapsing.

Over the weekend, even the Wall Street Journal is now catching up to what Natural News reported a year ago, admitting that covid-19 came from a lab. The article is entitled, “The Science Suggests a Wuhan Lab Leak” and carries the subhead, “The Covid-19 pathogen has a genetic footprint that has never been observed in a natural coronavirus.”

Authored by Steven Quay and Richard Muller, the article discusses the genetic fingerprint of the “double CGG” combination that appears in the virus:

Although the double CGG is suppressed naturally, the opposite is true in laboratory work. The insertion sequence of choice is the double CGG. That’s because it is readily available and convenient, and scientists have a great deal of experience inserting it. An additional advantage of the double CGG sequence compared with the other 35 possible choices: It creates a useful beacon that permits the scientists to track the insertion in the laboratory. Now the damning fact. It was this exact sequence that appears in CoV-2.

Despite this, the virologists involved in the gain-of-function research on coronavirus sought to hide the existence of this double CGG fingerprint:

When the lab’s Shi Zhengli and colleagues published a paper in February 2020 with the virus’s partial genome, they omitted any mention of the special sequence that supercharges the virus or the rare double CGG section. Yet the fingerprint is easily identified in the data that accompanied the paper. Was it omitted in the hope that nobody would notice this evidence of the gain-of-function origin?

But in a matter of weeks virologists Bruno Coutard and colleagues published their discovery of the sequence in CoV-2 and its novel supercharged site. Double CGG is there; you only have to look. They comment in their paper that the protein that held it “may provide a gain-of-function” capability to the virus, “for efficient spreading” to humans.

So it’s not just that SARS-CoV-2 was engineered in a lab; the scientists involved in that effort also tried to cover their tracks and deceive the world as millions died.

“The scientific evidence points to the conclusion that the virus was developed in a laboratory,” write Quay and Muller. Yes, we knew that a year ago. Now, the mainstream media is finally beginning to admit to the reality that those of us in the independent media have known all along.

Names you need to know: Peter Daszak (EcoHealth Alliance), Anthony Fauci, Ralph Baric

Some good sources of information about the communist Chinese bioweapons program that was funded by Daszak, Fauci and even the Pentagon:

RedState.com: EXCLUSIVE: High-Ranking Chinese Defector Has ‘Direct Knowledge’ of Several Chinese Special Weapons Programs

Wall Street Journal: The Science Suggests a Wuhan Lab Leak

UK Daily Mail: The Pentagon secretly funneled $39 to Peter Daszak, his charity funded the Wuhan lab

The National Pulse: Fauci’s Boss Admits Funding Wuhan Lab: ‘We Had No Control Over What They Were Doing.’

LifeSiteNews: China Virus “Smoking Gun” Found

The Bulletin of the Atomic Scientists: The origin of COVID: Did people or nature open Pandora’s box at Wuhan?

From the UK Daily Mail:

The Pentagon gave $39 MILLION to Dr. Peter Daszak’s EcoHealth Alliance – the charity that funded coronavirus research at the Wuhan lab accused of being the source of the outbreak, federal data reveals… Federal data seen by DailyMail.com reveals The Pentagon gave $39 million to EcoHealth Alliance, which funded a lab in Wuhan, China, between 2013 and 2020. The Wuhan Institute of Virology is accused of being the source of Covid-19.

From LifeSiteNews:

The Australian Strategic Policy Institute (ASPI) has just uncovered a Chinese book that proves that Chinese military scientists have been working towards the development of a “new era of genetic weapons.” These weapons, the Chinese scientists promised, could be “artificially manipulated into an emerging human disease virus, then weaponized and unleashed.”

In the 2015 volume, called The Unnatural Origin of SARS and New Species of Man-Made Viruses as Genetic Bioweapons, the Chinese military scientists begin by suggesting that World War III would be fought with biological weapons.

And not just any bioweapons.

Coronaviruses, a number of which cause respiratory illnesses in people, were mentioned as a class of viruses that could be readily weaponized. Indeed, the Chinese scientists were even more explicit, pointing out in their paper that the coronavirus that causes Severe Acute Respiratory Syndrome, or SARS, was an ideal candidate for a bioweapon.

From The Bulletin:

It later turned out that the Lancet letter had been organized and drafted by Peter Daszak, president of the EcoHealth Alliance of New York. Daszak’s organization funded coronavirus research at the Wuhan Institute of Virology. If the SARS2 virus had indeed escaped from research he funded, Daszak would be potentially culpable. This acute conflict of interest was not declared to the Lancet’s readers. To the contrary, the letter concluded, “We declare no competing interests.”

Virologists like Daszak had much at stake in the assigning of blame for the pandemic. For 20 years, mostly beneath the public’s attention, they had been playing a dangerous game. In their laboratories they routinely created viruses more dangerous than those that exist in nature. They argued that they could do so safely, and that by getting ahead of nature they could predict and prevent natural “spillovers…”

Researchers at the Wuhan Institute of Virology, led by China’s leading expert on bat viruses, Shi Zheng-li or “Bat Lady,” mounted frequent expeditions to the bat-infested caves of Yunnan in southern China and collected around a hundred different bat coronaviruses.

Shi then teamed up with Ralph S. Baric, an eminent coronavirus researcher at the University of North Carolina. Their work focused on enhancing the ability of bat viruses to attack humans so as to “examine the emergence potential (that is, the potential to infect humans) of circulating bat CoVs [coronaviruses].” In pursuit of this aim, in November 2015 they created a novel virus by taking the backbone of the SARS1 virus and replacing its spike protein with one from a bat virus (known as SHC014-CoV). This manufactured virus was able to infect the cells of the human airway, at least when tested against a lab culture of such cells.

Baric had developed, and taught Shi, a general method for engineering bat coronaviruses to attack other species. The specific targets were human cells grown in cultures and humanized mice.

Peter Daszak celebrates (brags) about engineering the SARS coronavirus to attack human cells

Also from TheBulletin.org:

Shi set out to create novel coronaviruses with the highest possible infectivity for human cells. Her plan was to take genes that coded for spike proteins possessing a variety of measured affinities for human cells, ranging from high to low. She would insert these spike genes one by one into the backbone of a number of viral genomes (“reverse genetics” and “infectious clone technology”), creating a series of chimeric viruses. These chimeric viruses would then be tested for their ability to attack human cell cultures (“in vitro”) and humanized mice (“in vivo”).

On December 9, 2019, before the outbreak of the pandemic became generally known, Daszak gave an interview in which he talked in glowing terms of how researchers at the Wuhan Institute of Virology had been reprogramming the spike protein and generating chimeric coronaviruses capable of infecting humanized mice.

“And we have now found, you know, after 6 or 7 years of doing this, over 100 new SARS-related coronaviruses, very close to SARS,” Daszak says around minute 28 of the interview. “Some of them get into human cells in the lab, some of them can cause SARS disease in humanized mice models and are untreatable with therapeutic monoclonals and you can’t vaccinate against them with a vaccine. So, these are a clear and present danger….

“Daszak: Well I think…coronaviruses?—?you can manipulate them in the lab pretty easily. Spike protein drives a lot of what happen with coronavirus, in zoonotic risk. So you can get the sequence, you can build the protein, and we work a lot with Ralph Baric at UNC to do this. Insert into the backbone of another virus and do some work in the lab.

In disjointed style, Daszak is referring to the fact that once you have generated a novel coronavirus that can attack human cells, you can take the spike protein and make it the basis for a vaccine.

Full details in today’s length Situation Update podcast

Today’s podcast provides the full details, covering the origins of covid, the cover-up attempt and the collapse of the cover-up. Now we know that the spike protein used in covid vaccines is actually a communist Chinese military bioweapon.

We also therefore know that covid-19 vaccines are biological weapons designed to exterminate humanity, since they contain the weaponized spike protein that was specifically engineered to attack human ACE2 receptors, which exist all over the body (not just the lungs).

Remember, Fauci and Daszak helped fund the development of genetically engineered “humanized mice” — mice with human lung tissue — in order to maximize the ability of the virus to infect human beings. This is all now admitted.

Hear the full podcast on Brighteon.com:

 

COVID Vaccine Spike Protein Travels From Injection Site, Can Cause Organ Damage

‘We Made a Big Mistake’ — COVID Vaccine Spike Protein Travels From Injection Site, Can Cause Organ Damage

Research obtained by a group of scientists shows the COVID vaccine spike protein can travel from the injection site and accumulate in organs and tissues including the spleen, bone marrow, the liver, adrenal glands and in “quite high concentrations” in the ovaries.

By Megan Redshaw

COVID vaccine researchers had previously assumed mRNA COVID vaccines would behave like traditional vaccines. The vaccine’s spike protein — responsible for infection and its most severe symptoms — would remain mostly in the injection site at the shoulder muscle or local lymph nodes.

But new research obtained by a group of scientists contradicts that theory, a Canadian cancer vaccine researcher said last week.

“We made a big mistake. We didn’t realize it until now,” said Byram Bridle, a viral immunologist and associate professor at University of Guelph, Ontario. “We thought the spike protein was a great target antigen, we never knew the spike protein itself was a toxin and was a pathogenic protein. So by vaccinating people we are inadvertently inoculating them with a toxin.”

 

Bridle, who was awarded a $230,000 grant by the Canadian government last year for research on COVID vaccine development, said he and a group of international scientists filed a request for information from the Japanese regulatory agency to get access to Pfizer’s “biodistribution study.”

Biodistribution studies are used to determine where an injected compound travels in the body, and which tissues or organs it accumulates in.

“It’s the first time ever scientists have been privy to seeing where these messenger RNA [mRNA] vaccines go after vaccination,” Bridle said in an interview with Alex Pierson where he first disclosed the data. “Is it a safe assumption that it stays in the shoulder muscle? The short answer is: absolutely not. It’s very disconcerting.”

The Sars-CoV-2 has a spike protein on its surface. That spike protein is what allows it to infect our bodies, Bridle explained. “That is why we have been using the spike protein in our vaccines,” Bridle said. “The vaccines we’re using get the cells in our bodies to manufacture that protein. If we can mount an immune response against that protein, in theory we could prevent this virus from infecting the body. That is the theory behind the vaccine.”

“However, when studying the severe COVID-19, […] heart problems, lots of problems with the cardiovascular system, bleeding and clotting, are all associated with COVID-19,”  he added. “In doing that research, what has been discovered by the scientific community, the spike protein on its own is almost entirely responsible for the damage to the cardiovascular system, if it gets into circulation.”

When the purified spike protein is injected into the blood of research animals, they experience damage to the cardiovascular system and the protein can cross the blood-brain barrier and cause damage to the brain, Bridle explained.

The biodistribution study obtained by Bridle shows the COVID spike protein gets into the blood where it circulates for several days post-vaccination and then accumulates in organs and tissues including the spleen, bone marrow, the liver, adrenal glands and in “quite high concentrations” in the ovaries.

“We have known for a long time that the spike protein is a pathogenic protein, Bridle said. “It is a toxin. It can cause damage in our body if it gets into circulation.”

A large number of studies have shown the most severe effects of SARS-CoV-2, the virus that causes COVID, such as blood clotting and bleeding, are due to the effects of the spike protein of the virus itself.

A recent study in Clinical and Infectious Diseases led by researchers at Brigham and Women’s Hospital and the Harvard Medical School measured longitudinal plasma samples collected from 13 recipients of the Moderna vaccine 1 and 29 days after the first dose and 1-28 days after the second dose.

Out of these individuals, 11 had detectable levels of SARS-CoV-2 protein in blood plasma as early as one day after the first vaccine dose, including three who had detectable levels of spike protein. A “subunit” protein called S1, part of the spike protein, was also detected.

Spike protein was detected an average of 15 days after the first injection, and one patient had spike protein detectable on day 29 — one day after a second vaccine dose — which disappeared two days later.

The results showed S1 antigen production after the initial vaccination can be detected by day one and is present beyond the injection site and the associated regional lymph nodes.

Assuming an average adult blood volume of approximately 5 liters, this corresponds to peak levels of approximately 0.3 micrograms of circulating free antigen for a vaccine designed only to express membrane-anchored antigen.

In a study published in Nature Neuroscience, lab animals injected with purified spike protein into their bloodstream developed cardiovascular problems. The spike protein also crossed the blood-brain barrier and caused damage to the brain.

It was a grave mistake to believe the spike protein would not escape into the blood circulation, according to Bridle. “Now, we have clear-cut evidence that the vaccines that make the cells in our deltoid muscles manufacture this protein — that the vaccine itself, plus the protein — gets into blood circulation,” he said.

Bridle said the scientific community has discovered the spike protein, on its own, is almost entirely responsible for the damage to the cardiovascular system, if it gets into circulation.

Once in circulation, the spike protein can attach to specific ACE2 receptors that are on blood platelets and the cells that line blood vessels, Bridle said. “When that happens it can do one of two things. It can either cause platelets to clump, and that can lead to clotting — that’s exactly why we’ve been seeing clotting disorders associated with these vaccines. It can also lead to bleeding,” he added.

Both clotting and bleeding are associated with vaccine-induced thrombotic thrombocytopenia (VITT). Bridle also said the spike protein in circulation would explain recently reported heart problems in vaccinated teens.

Stephanie Seneff, senior research scientists at Massachusetts Institute of Technology, said it is now clear vaccine content is being delivered to the spleen and the glands, including the ovaries and the adrenal glands, and is being shed into the medium and then eventually reaches the bloodstream causing systemic damage.

“ACE2 receptors are common in the heart and brain,” she added. “And this is how the spike protein causes cardiovascular and cognitive problems.”

Dr. J. Patrick Whelan, a pediatric rheumatologist, warned the U.S. Food and Drug Administration (FDA) in December mRNA vaccines could cause microvascular injury to the brain, heart, liver and kidneys in ways not assessed in safety trials.

In a public submission, Whelan sought to alert the FDA to the potential for vaccines designed to create immunity to the SARS-CoV-2 spike protein to instead cause injuries.

Whelan was concerned the mRNA vaccine technology utilized by Pfizer and Moderna had “the potential to cause microvascular injury (inflammation and small blood clots called microthrombi) to the brain, heart, liver and kidneys in ways that were not assessed in the safety trials.”

More Deaths Reported After J&J, AstraZeneca Vaccines, Plus Researchers Link AstraZeneca to Strokes in Young Adults

More Deaths Reported After J&J, AstraZeneca Vaccines, Plus Researchers Link AstraZeneca to Strokes in Young Adults

The AstraZeneca and Johnson & Johnson COVID vaccines came under scrutiny again this week as more reports of deaths — largely due to blood clot disorders — surfaced in Belgium, Canada and Greece, and a new report linked the AstraZeneca vaccine to strokes in young adults.

By Megan Redshaw

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The AstraZeneca and Johnson & Johnson (J&J) COVID vaccines came under scrutiny again this week as more reports of deaths — largely due to blood clot disorders — surfaced in Belgium, Canada and Greece.

Adding to the vaccine makers’ woes is a new report out of London from researchers who identified the first cases of strokes occurring in young adults who received the AstraZeneca vaccine, which was co-developed by the University of Oxford University in the UK.

Belgium suspends use of J&J vaccine

Belgium said Wednesday it was suspending vaccinations with J&J vaccine, for people under the age of 41, following the death of a woman from blood clots after she received the shot. This is the second time Belgium has paused the one-shot vaccine.

“The Inter-ministerial conference has decided to temporarily administer Janssen’s vaccine to the general population from the age of 41 years, pending a more detailed benefit-risk analysis by the EMA,” said a statement issued by Belgium’s federal health minister and seven regional counterparts.

The woman, who was under the age of 40, died May 21 after being admitted to the hospital with severe thrombosis and platelet deficiency, Reuters reported.

The government asked for urgent advice from the European Union’s drug regulator, the European Medicines Agency (EMA), before it would consider lifting the suspension.

The EMA said it is reviewing the death of the woman in Belgium, along with other reports of blood clots, with the Belgian and Slovenian medicines agencies, and has asked J&J to carry out a series of additional studies to help assess a possible link between the shot and rare blood clots.

J&J said April 20 it would resume the roll-out in the EU of its COVID vaccine, marketed under the company’s Janssen subsidiary — with a warning on its label — after several countries, including Belgium, first paused the vaccine amid concerns of its possible link to blood clotting disorders.

The EMA confirmed a “possible link,” but concluded the vaccine’s benefits outweighed the risks. The drug regulator’s safety committee (PRAC) said a warning should be added to the product label, but the blood clot-related disorders should be listed as “very rare” side effects of the vaccine.

On April 23, the Centers for Disease Control and Prevention (CDC) voted to resume the use of J&J’s vaccine without restrictions after the vaccine was paused to investigate reports of rare blood clots. The recommendation by the CDC’s advisory panel said the link between blood clots and J&J’s COVID vaccine was “plausible,” but concluded the vaccine’s benefits outweighed the risks and recommended use for persons 18 years of age and older in the U.S. under the FDA’s Emergency Use Authorization.

J&J has said no clear causal relationship has been established between its vaccine and blood clots.

Researchers identify strokes in young adults after AstraZeneca shot

The first cases of large-vessel arterial occlusion strokes in young adults linked to AstraZeneca’s vaccine were described in detail for the first time in a letter published online in the Journal of Neurology Neurosurgery & Psychiatry.

The three cases, one of which was fatal, occurred in two women and one man in their 30s or 40s who developed characteristics of vaccine-induced immune thrombotic thrombocytopenia (VITT), a reaction associated with the AstraZeneca vaccine.

“These are the first detailed reports of arterial stroke believed to be caused by VITT after the AstraZeneca COVID vaccine, although stroke has been mentioned previously in the VITT data,” senior author, Dr. David Werring, professor of clinical neurology at the Stroke Research Centre, University College London Queen Square Institute of Neurology, told Medscape Medical News.

“VITT has more commonly presented as CVST (cerebral venous sinus thrombosis) which is stroke caused by a venous thrombosis; these cases are showing that it can also cause stroke caused by an arterial thrombosis,” Werring explained.

Werring noted the reports do not add anything to the overall risk/benefit of the vaccine, as they are describing only three cases. “While VITT is very serious, the benefit of the vaccine still outweighs its risks,” he said.

The first case, a 35-year-old woman, experienced intermittent headaches on the right side and around her eyes for six days after vaccination. Five days later, she awoke feeling drowsy and with weakness to her left face, arm and leg.

Imaging revealed the woman had a blocked right middle cerebral artery with brain infarction and clots in the right portal vein. She underwent brain surgery to reduce the pressure in her skull, plasma removal and replacement, and treatment with anticoagulant and fondaparinux, but suffered brain stem death and subsequently died.

The second case, a 37-year-old woman, presented with headache, confusion, weakness in her left arm and loss of vision on the left side 12 days after vaccination with AstraZeneca. Imaging showed occlusion of both carotid arteries, as well as blood clots in her lungs and brain. She improved clinically with treatment.

The third case occurred in a 43-year-old man who presented 21 days after vaccination with problems speaking. Imaging showed a clot in the left middle cerebral artery. He was treated and remains stable.

The researchers said young patients presenting with ischaemic stroke after receiving AstraZeneca’s vaccine should urgently be evaluated for VITT.

Ontario man dies from ‘rare but real’ blood clot after first dose of AstraZeneca

An Ontario man in his 40s died after receiving his first dose of the AstraZeneca vaccine, public health officials confirmed Tuesday.

Dr. Barbara Yaffe, Ontario’s associate chief medical officer of health, said his death is being investigated, but the man suffered from VITT.

“While the investigation is ongoing and a final cause of death has yet to be officially determined, it has been confirmed that the individual did have VITT at the time of his death,” Yaffe said Tuesday. “The risks associated with this vaccine are [rare], but they are real.”

Chief Medical Officer Dr. David Williams restricted AstraZeneca vaccinations for people who have not yet received the first dose as of May 11, due to a higher-than-expected rate of blood clots.

Greece investigating four cases of blood clots after AstraZeneca shot

Α 63-year-old woman from Greece died of blood clots after vaccination with AstraZeneca. The case was one of four being investigated by the National Organization for Medicines (EOF) for a potential correlation between AstraZeneca’s vaccine and rare blood clots, according to the Greek City Times.

Also in Greece, a 44-year-old woman is in serious condition after experiencing VITT. Her case was the second incident found by EOF to be linked to the vaccine, according to the Greek Reporter.

A third blood clotting incident involved a 35-year-old man from Crete who suffered two blood clots after receiving AstraZeneca’s vaccine. The man was hospitalized after suffering a clot in his leg a few days after getting the jab. He suffered a second blood clot in his brain while hospitalized

As The Defender reported April 7, European regulators said they confirmed a “possible link” between AstraZeneca’s COVID vaccine and “very rare” blood clots, but concluded the benefits of the vaccine still outweigh the risks.

The EMA did not recommend restricting use of the vaccine based on age, gender or other risk factors, but did say cases of blood clotting after vaccination “should be” listed as a possible side effect, according to a statement issued by the agency’s safety committee.

The AstraZeneca vaccine is not yet authorized for use in the U.S.

Nobel Prize winner: Mass COVID vaccination an ‘Unacceptable Mistake’ that is ‘Creating the Variants’

Nobel Prize Winner: Mass Vaccination an "Unacceptable Mistake"

In every country, ‘the curve of vaccination is followed by the curve of deaths,’ the famous virologist said

 

As published on LifeSite News by Celeste McGovern

French virologist and Nobel Prize winner Luc Montagnier called mass vaccination against the coronavirus during the pandemic “unthinkable” and a historical blunder that is “creating the variants” and leading to deaths from the disease.

“It’s an enormous mistake, isn’t it? A scientific error as well as a medical error. It is an unacceptable mistake,” Montagnier said in an interview translated and published by the RAIR Foundation USA yesterday. “The history books will show that, because it is the vaccination that is creating the variants.”

 

Many epidemiologists know it and are “silent” about the problem known as “antibody-dependent enhancement,” Montagnier said.

“It is the antibodies produced by the virus that enable an infection to become stronger,” he said in an interview with Pierre Barnérias of Hold-Up Media earlier this month. 

Vaccination leading to variants

“It is clear that the new variants are created by antibody-mediated selection due to the vaccination.”

Vaccinating during a pandemic is “unthinkable” and is causing deaths, the winner of the 2008 Nobel Prize in Medicine for discovery

‘Deaths follow vaccination’

“The new variants are a production and result from the vaccination. You see it in each country, it’s the same: in every country deaths follow vaccination,” he said.

A video published last week on YouTube uses data from the Institute for Health Metrics and Evaluation at the University of Washington to illustrate the spikes in deaths in numerous countries across the globe after the introduction of COVID vaccination, confirming Montagnier’s observation.

The French interviewer pointed to data from the World Health Organization(WHO) showing that since the vaccines were introduced in January, new infections contamination have “exploded,” along with deaths, “notably among young people.”

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“Yes,” agreed Montagnier who is a professor at Shanghai Jiao Tong University. “With thrombosis, etc.”

Thrombosis – or blood clots — have been an unexpected problem linked to the new coronavirus vaccines and the cause of AstraZeneca’s vaccine being pulled in several countries. The head of Canada’s public health agency, Theresa Tam, told a press conference Tuesday that there are now 21 confirmed cases of vaccine-induced thrombotic thrombocytopenia, or VITT, including among three women who died from the blood-clotting disorder potentially linked to AstraZeneca’s vaccine and another 13 cases are under investigation. 

Breakthrough cases

Montagnier said that he is currently conducting research with those who have become infected with the coronavirus after getting the vaccine. The Centers for Disease Control and Prevention reported in April that it had received 5,800 reports of people who had “breakthrough” COVID after being vaccinated, including 396 people who required hospitalization and 74 patients who died. 

“I will show you that they are creating the variants that are resistant to the vaccine,” Montagnier said.

Coronavirus made in a lab

The famous French virologist created waves in April 2020 when he told a French television station that he believed SARS-CoV2, the new pandemic coronavirus, was man-made in a laboratory. The “presence of elements of HIV and germ of malaria in the genome of coronavirus is highly suspect and the characteristics of the virus could not have arisen naturally,” he said

Though he was ridiculed by French experts for having “a conspiracy vision that does not relate to the real science,” Montagnier published a paper in July 2020 supporting his claims that the novel coronavirus must have originated from human experimentation in a lab – a theory that has recently resurfaced and is currently considered the most likely origin of the virus.

 

To view the original article, please click here

 

 

 

Government Caught “Scrubbing” Covid-19 Vaccine Injuries and Deaths

Government caught "scrubbing" Covid-19 vaccine injuries and deaths

Dr. Peter McCullough, one of the world’s premiere medical doctors who specializes in treating the Wuhan coronavirus (Covid-19), told journalist Alex Newman during a recent interview that the United States government is lying about the true number of Chinese Virus vaccine reactions that are occurring. The government’s strategy, McCullough says, which is coordinated with the Bill & Melinda Gates Foundation and the World Health Organization (WHO), has resulted in tens of thousands of unnecessary deaths that are being ignored or swept under the rug. This is unprecedented because the government has pulled past drugs and vaccines from the market for far less. Between Dec. 14 and April 23, Donald Trump’s “Operation Warp Speed” jabs caused at least 3,544 deaths along with 12,619 serious injuries. Neither the Food and Drug Administration (FDA) nor the Centers for Disease Control and Prevention (CDC), however, are at all concerned. “A typical new drug at about five deaths, unexplained deaths, we get a black-box warning, your listeners would see it on TV, saying it may cause death,” McCullough stated. “And then at about 50 deaths, it’s pulled off the market.” Back in 1976 during the “swine flu” crisis, the U.S. attempted to jab some 55 million Americans but stopped the program after 500 cases of paralysis and 25 deaths were reported. Compare that to the Wuhan Flu shots of today, which are still being aggressively pushed despite untold thousands of injuries and deaths. “In the U.S. today [as of late March] we have approximately 77 million people vaccinated for COVID and we have 2,602 deaths reported, so it’s unprecedented how many deaths have accrued,” McCullough further explained. “Then on March 8 the CDC announced on their website with very little fanfare that they had reviewed about 1,600 deaths with unnamed FDA doctors and they indicated not a single death was related to the vaccine. he added. I think that was concerning in the academic community.”

Wuhan Flu shots are mass genocide

Had the CDC truly conducted such an investigation, McCullough says, it would have taken months to complete. Instead, the CDC rolled it out in a matter of days to declare all of the jabs “safe and effective” so the program would continue. “I have chaired and participated in dozens of data safety monitoring boards and sat on those committees and I can tell you that this type of work would have taken many months to review all the labs, the death certificates and all the circumstances of an event,” McCullough explained. “It is impossible for unnamed regulatory doctors without any experience with COVID-19 to opine that none of the deaths were related to the vaccine.” Another factor to consider is that only about 1-10 percent of all vaccine-related deaths even get logged into the CDC’s Vaccine Adverse Event Reporting System (VAERS). This suggests that many thousands more deaths are not even included in the official numbers. Even without this missing data, Chinese Virus injections are already proving to be far more dangerous than seasonal flu shots. Every year, 20-30 deaths from flu shots are reported to VAERS based on 195 million injections. Wuhan Flu shots, on the other hand, have already caused at least 2,602 deaths based on 77 million injections. “So the U.S. government has made a decision, along with the stakeholders – the CDC, NIH, FDA, Big Pharma, World Health Organization, Gates Foundation – they have made a commitment to mass vaccination as the solution to the COVID pandemic and we are really going to be witness to what’s going to happen in history,” McCullough warns. “We’re sitting on, right now, the biggest number of vaccine deaths, there’s been tens of thousands of hospitalizations, all attributable to the vaccine, and going strong.” More related news can be found at Pandemic.news

Sources for this article include: LeoHohmann.com NaturalNews.com

19,916 ‘eye disorders’ including blindness following COVID vaccine reported in Europe

19,916 ‘eye disorders’ including blindness following COVID vaccine reported in Europe

More than 10,000 reports of eye disorders after COVID shots in the U.K. alone

By Celeste McGovern

May 1, 2021 (LifeSiteNews) – Hundreds of cases of blindness are among the 19,916 reports of “eye disorders” to the World Health Organization’s European drug monitoring agency following injection of experimental COVID-19 vaccines

The nearly 20,000 eye disorders reported to VigiBase, a database for the WHO maintained by the Uppsala Monitoring Centre(UMC) in Uppsalla, Sweden, include:

  • Eye pain (4616)
  • Blurred vision  (3839)
  • Photophobia or light intolerance (1808)
  • Visual impairment (1625)
  • Eye swelling (1162)
  • Ocular hyperaemia or red eyes (788)
  • Eye irritation (768)
  • Itchy eyes or eye pruritus (731)
  • Watery eyes or increased lacrimation (653)
  • Double vision or diplopia (559)
  • Eye strain or asthenopia (459)
  • Dry eye (400)
  • Swelling around the eye or periorbital swelling (366)
  • Swelling of eyelid (360)
  • Flashes of light in the field of vision or photopsia (358)
  • Blindness (303)
  • Eyelid oedema (298)
  • Eye or ocular discomfort (273)
  • Conjunctival haemorrhage or breakage of a small eye vessel (236)
  • Blepharospasm or abnormal contraction of an eye muscle(223)
  • Vitreous floaters (192)
  • Periorbital oedema (171)
  • Eye haemorrhage (169)

More than half of the eye disorders (10, 667) were also reported to the U.K.’s Yellow Card adverse event reporting system. These would have followed injection primarily of AstraZeneca’s and Pfizer’s COVID-19 vaccines but included eight reports of eye disorders among the 228 reports concerning Moderna’s vaccine, of which only 100,000 first doses had been administered by April 21.

Eye disorders were not reported in the clinical trials for vaccines which have been granted Emergency Use Authorization (EUA) only. The U.S. Food and Drug Administration’s fact sheet for those administering Pfizer’s experimental vaccine does not mention eye side effects. It does state, however, that “Additional adverse reactions, some of which may be serious, may become apparent with more widespread use of the Pfizer-BioNTech COVID-19 Vaccine.”

VAERS reports

VigiBase and Yellow Card reports do not offer details of the patients’ experiences of adverse side-effects. However, those in the U.S. Vaccine Adverse Event Reporting System (VAERS) system include some reporting on the patient, his or her age, and the general case presentation.

One VAERS report describes a 33-year-old pilot from Mississippi who took Pfizer’s vaccine and developed vision problems among numerous other symptoms.

“I noticed a headache in the very top of my head within an hour of getting the vaccine,” he reported. “I thought it was normal because everyone I know said they got a headache from it. Over the next few hours, the pain moved down the back of my neck and became a burning sensation at the bottom of my skull.”

“Two days after receiving the vaccine I flew my plane and immediately noticed something was wrong with me,” the report continues. “I was having a very hard time focusing. Approximately 2 hours into my flying I felt sudden and extreme pressure in my head and nearly blacked out. I immediately landed and stopped flying.”

The pilot experienced the same thing two days later when he tried flying again. The burning in his neck intensified and was accompanied by dizziness, nausea, disorientation, confusion, uncontrollable shaking, and tingling in his toes and fingers.

The patient was diagnosed with vertigo and prescribed a medication which provided “no relief,” according to the VAERS account. He underwent extensive testing including balance, eye, and hearing tests, CT and MRI scans, and he was informed that an allergic reaction to the Pfizer COVID vaccine had increased the pressure in his spinal cord and brain stem.

“That pressure causes my vision problems and ultimately ruptured my left inner ear breaking off several crystals in the process,” the report states.  “I cannot fly with this condition. I’m currently taking Diamox to reduce the pressure in my spinal cord and brain stem.”

More than 1,200 reports to VAERS include “eye pain” among the listed symptoms. One report filed by a 50-year-old physician from Wisconsin for himself said he experienced “severe sweating; fever; weakness” and the “worst headache of my life” following receiving a second dose of Pfizer’s Wuhan coronavirus vaccine in January.  The doctor said he experienced “searing eye pain for the last 2 months” and “daily headaches” – events described as a “disability” and “permanent damage.”

One 26-year-old student in California received Johnson & Johnson’s vaccine on April 9 and reported experiencing “typical” post-vaccine symptoms of nausea, muscle aches, chills, fatigue which “dissipated.” On the fifth day following the shot, however, she went for a light walk in the morning and “completely lost vision in both eyes.” She also described her “excruciating headache behind eyes” as the “worst headache of my life.” At a hospital emergency ward she was given morphine which she reported did not help the pain and a head CT scan ruled out a clotting event. Her report filed six days later, said: “I’m terrified because I know something is very wrong.”

‘Frightening, stressful, and uncertain’

Michelle Jorgenson, 31, of Arizona got her first dose of Moderna’s vaccine in mid-January, and second dose mid-February and developed blurred vision along with symptoms of headaches, “brain fog” and fatigue. She’s undergone CT and MRI scans and doctors don’t know what’s causing her problems,” she said.

“It’s frightening, stressful, and uncertain. I’m 31, and I have never in my life had double vision before,” she says.

Jorgenson said illness is affecting her ability to both work and drive. “I’m not currently driving at all, as it is just not safe.”

She has cut her at-home work schedule from 40 hours per week to about 25 hours per week, “but that’s also a struggle, because of the double vision, headache, brain fog, and fatigue.”

“I don’t know what the doctors can do from here,” she said.

Bleeding and clotting disorders

Numerous vision problems are associated with hemorrhaging and blood clotting incidents:

  • A 25-year-old from Massachusetts began experiencing symptoms on the day of receiving her first dose of Moderna’s vaccine in January and an MRI revealed “inflammation, and brain bleed and swelling,” according to the VAERS reportfiled by a healthcare professional.
  • An 83 year-old from Indiana who had Moderna’s vaccine and went blind in her left eye the same day. “Went to emergency room at Hospital Was told I have Blood clot in my eye causing the blindness and Ophthamologist says it will probably be permanent,” her report states.
  • A 50-year-old woman from Oklahoma with no prior health conditions experienced a central retinal vein occlusion (CRVO) 2 and ½ hours after receiving a second dose of Pfizer’s COVID-19 vaccine resulted in loss of sight to her right eye, according to another VAERS report. “I am currently prescribed baby aspirin and will have to get injections in my eye when macular edema occurs, an expected occurrence with a blood clot in the retinal vein.”
  • “Within 12 hours of receiving the 2nd dose of the Moderna vaccine, I experienced an occipital cerebral infarction in the left occipital lobe,” states the VAERS report of a 73-year-old Florida man. “As a result, I have a loss of peripheral vision in the right upper quadrant.”
  • Another VAERS report describes a 68-year-old California man’s four-day hospitalization and numerous interventions after his first dose of Pfizer’s vaccine: “Permanent loss of vision in right eye three weeks after receiving first COVID 19 vaccination. Diagnosed with Branch Retina Artery Occlusion (BRAO) clotting of the retinal artery.”

Previous coronavirus

Pennsylvania immunologist Hooman Noorchashm has warned about the potential for vaccinating the 20% to 30% of people who have already had a recent or underlying COVID infection may lead to catastrophic events. That may be the reason why a 52-year-old man from Michigan who was diagnosed with COVID-19 on December 13, 2020 who then received a series of shots on December 22 and January 10, 2021 was diagnosed one day after his second shot with opthalmic artery thrombus causing vision loss in his left eye.

Allergic eye disorders

Some eye disorders happened in the context of severe allergic or “anaphylactic” or “anaphylactoid” events for which there are 915 VAERS report. More than 60 reports refer to “anaphylaxis” and eye symptoms in the same event, as in the case of a 55-year-old asthmatic woman with food allergies who had a reaction to Pfizer’s second dose of COVID vaccine and according a VAERS report was put “under the care of an eye doctor for her severe double vision, eye crossing, and eye drooping.”

Shingles

Some eye pain reports are in association with herpes – or shingles — infection, which has already been raised as a potential elevated risk factor following COVID vaccination. According to a report on one 30-year-old woman, her “severe right side eye pain” and “vesicular rash with severe pain above right eyelid” developed after she got her Johnson & Johnson one-shot in January. She was diagnosed with Zoster Ophthalmicus of Right Eye and treated in urgent care. After her rash crusted she still had residual severe neuropathic pain at the time of the report nine days later.

Uveitis

In Great Britain, 35 reports of uveitis – an inflammation of the middle layer of the eye – following coronavirus vaccination were generated by April 21, about four months following the vaccines rollout in December.

This may seem a small number except that one 2016 study that looked for cases of “vaccine-associated” uveitis found 289 reports over 26 years of data from three databases – which works out to about 11 cases per year for all vaccinations. In which case, reports for uveitis are many fold higher than what one would expect to see from vaccination.

“The nature of Yellow Card reporting means that reported events are not always proven side effects,” according to the government website that catalogues the reports. “Some events may have happened anyway, regardless of vaccination.”

While public health officials have frequently stated that vaccine adverse events are only “one or two in a million” shots, the Medicines and Healthcare products Regulatory Agency (MHRA) for Britain states that for the Pfizer/BioNTech and AstraZeneca vaccines, the overall reporting rate is “around 3 to 6 Yellow Cards per 1,000 doses administered.”

As well, because both the U.S. VAERS the U.K. Yellow Card are passive collections systems, they tend to capture only a fraction of adverse events. A Harvard Pilgrim Healthcare study found that less than one percent of vaccine adverse events are reported to VAERS.

Asked about the high numbers of reported adverse eye events, a spokesperson for the MHRA, which oversees Yellow Card reports, said in an emailed statement: “We continually review Yellow Card data, as well as other data sources, to determine if reports may indicate any previously unrecognised risks.”

The statement added that the agency applies “statistical techniques” which compare events to what would be expected generally in the population.  

“Everything has to be looked at on a case by case basis, and there is no set trigger to determine whether something may be linked to a vaccine,” the MHRA statement said. “All reports are kept under review taking into account the information available and whether there are other plausible explanations.”

Among the 12,140 adverse events reported to Canada’s coronavirus vaccine adverse event reporting system by April 23, there is not a single account of an eye disorder— which, given the extraordinarily high numbers in other countries, raises questions about Canada’s reporting process.

COVID-Vaccinated Can ‘Shed’ Spike Protein, Harming Unvaccinated

America’s Frontline Doctors: COVID-vaccinated can ‘shed’ spike protein, harming unvaccinated

As these experimental vaccines create ‘spike proteins,’ vaccinated individuals ‘can shed some of these particles to close contacts’ causing disease in them, including in children.

By Patrick Delaney

 

LOS ANGELES, California, May 3, 2021 (LifeSiteNews) — In their latest issue brief, America’s Frontline Doctors (AFLDS) warned how spike proteins resulting from experimental COVID-19 gene therapy vaccines have the capacity to 1.) pass through the “blood-brain barrier” causing neurological damage, 2.) be “shed” by the vaccinated, bringing about sickness in unvaccinated children and adults, and 3.) cause irregular vaginal bleeding in women.

Released last week and titled “Identifying Post-vaccination Complications & Their Causes: an Analysis of Covid-19 Patient Data,” the stated purpose of the document is “to provide additional information for concerned citizens, health experts, and policymakers about adverse events and other post-vaccination issues resulting from the three experimental COVID-19 vaccines currently administered under EUA (emergency use authorization)” by the U.S. Food and Drug Administration (FDA).

The non-profit organization highlighted the thousands of adverse events which are related to these “vaccines” and captured by the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS). “Yet these complications have received a fraction of the attention paid to J&J’s blood-clotting controversy,” they lamented with dismay, asking, “Why?”

In taking a closer look at this data, AFLDS presents “some major categories of concern as-yet publicly unaddressed by either the FDA or CDC,” asserting that failure of these regulators “to consider these and other ‘known unknowns’ is a dereliction of basic medical research.”

They breakout their general categories of concern as shown below:

First, there are significant fears regarding the wide distribution of these new vaccines, which employ a new technology and remain only experimental without full approval from the FDA. Instead of employing an attenuated antigen response – as happens with conventional vaccines – these experimental agents introduce something called a “spike protein” into one’s system.

“It takes years to be sure something new is safe,” the AFLDS document confirms. “No one knows definitively the long-term health implications for the body and brain, especially among the young, related to this spike protein. In addition, if documented problems with the protein do arise, there will never be any way to reverse the adverse effects in those already vaccinated.”

Second, unlike conventional vaccines, these spike proteins, along with “lipid nanoparticles” have the capacity to pass through the “blood-brain barrier” which provides special protection for these sensitive areas of the body.

“There simply has not been enough time to know what brain problems and how often a brain problem will develop from that,” the document warns.

Risks from such penetration include “chronic inflammation and thrombosis (clotting) in the neurological system, contributing to tremors, chronic lethargy, stroke, Bell’s Palsy and ALS-type symptoms. The lipid nanoparticles can potentially fuse with brain cells, resulting in delayed neuro-degenerative disease. And the mRNA-induced spike protein can bind to brain tissue 10 to 20 times stronger than the spike proteins that are (naturally) part of the original virus.”

Third, as these experimental vaccines produce many trillions of spike proteins in their recipients, these vaccinated individuals “can shed some of these (spike protein) particles to close contacts,” causing disease in them.

In an email correspondence with LifeSiteNews, Dr. Simone Gold, the founder of AFLDS, directed this writer to an April 29 tweet where she posted a document from Pfizer’s experimental trials in which the pharmaceutical giant “acknowledges this mechanism” of potential shedding, she wrote. 

As the document states, one can be “exposed to [the] study intervention due to environmental exposure,” including “by inhalation or skin contact” with someone involved in the study, or with another who has been exposed in the same way.

And this, according to AFLDS, can be dangerous. As the issues brief continues, “the spike proteins are pathogenic (‘disease causing’) just like the full virus.” Furthermore, these “spike proteins bind more tightly than the fully intact virus” and thus cases around the world of “pericarditis, shingles, pneumonia, blood clots in the extremities and brain, Bell’s Palsy, vaginal bleeding and miscarriages have been reported in persons who are near persons who have been vaccinated.” Such shedding also “appears to be causing wide variety of autoimmune disease (where the body attacks its own tissue) in some persons.”

In addition, other more serious dangers to even the unvaccinated are possible due to the fact that these “spike proteins can cross the blood brain barrier, unlike traditional vaccines.”

Fourth, such shedding leaves children vulnerable if they are in proximity to parents and teachers who have received these experimental vaccines. While the threat of COVID-19 to the young is rightly described as “irrelevant,” including a 99.997% survival rate for those under 20 years of age, AFLDS is concerned some children may become symptomatic due to such proximity to the vaccinated. At such point there is a danger that “public health bureaucrats” might use such cases to “speculate that a child’s illness is related to a SARS-CoV-2 ‘variant,’” when it is a result of contact with vaccinated adults.

“Our other concern is that children could develop long-term chronic autoimmune disease including neurological problems due to the fact that children have decades ahead of them and trillions of the spike proteins mentioned above.”

Fifth, “AFLDS is aware of thousands of reports involving vaginal bleeding, post-menopausal vaginal bleeding, and miscarriages following COVID-19 vaccination as well as anecdotal reports of similar adverse events among those in close contact with the vaccinated.” While at this point the independent physicians organization “cannot comment definitively on the close contacts” other than to mention they “have heard reports of this worldwide,” the many reported incidents of post-vaccination vaginal bleeding establishes a clear “connection between the vaccine and irregular bleeding.”

“Despite this clear-cut evidence, menstrual-cycle changes were not listed among the FDA’s common side effects in its phase-three clinical participants. Women’s reproductive health needs to be taken seriously rather than waved away by agenda-driven public health officials,” the brief reads.

Finally, acknowledging the “irrepressible economic incentive among pharmaceutical companies” to market unnecessary and dangerous childhood COVID vaccinesboosters, and the like, AFLDS insists “Public health experts should stop and assess data on possible vaccine side effects and related post-vaccination questions before it is too late.”