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Vaccine Deaths & Injuries on the Rise

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Alarming Casualty Rates for mRNA Vaccines Warrant Urgent Action
By F. William Engdahl
19 May 2021
As official government data is emerging in Europe and the USA on the alarming numbers of deaths and permanent paralysis as well as other severe side effects from the experimental mRNA vaccines, it is becoming clear that we are being asked to be human guinea pigs in an experiment that could alter the human gene structure and far worse. While mainstream media ignores alarming data including death of countless healthy young victims, the politics of the corona vaccine is being advanced by Washington and Brussels along with WHO and the Vaccine Cartel with all the compassion of a mafia “offer you can’t refuse .”

The alarming EMA Report

On May 8 the European Medicines Agency (EMA) an agency of the European Union (EU) in charge of the evaluation and supervision of medical products, using the data base EudraVigilance which collects reports of suspected side effects of medicines including vaccines, published a report that barely warranted mention in major mainstream media. Through May 8, 2021 they had recorded 10,570 deaths and 405,259 injuries following injections of four experimental COVID-19 shots: COVID-19 mRNA VACCINE of MODERNA (CX-024414); COVID-19 mRNA VACCINE of PFIZER-BIONTECH; COVID-19 VACCINE of ASTRAZENECA (CHADOX1 NCOV-19); and Johnson & Johnson’s Janssen COVID-19 VACCINE (AD26.COV2.S).

A detailed analysis of each vaccine gives the following: The Pfizer-BioNTech mRNA gene-edited vaccine resulted in the largest fatalities– 5,368 deaths and 170,528 injuries or nearly 50% of the total for all four. The Moderna mRNA vaccine was second with 2,865 deaths and 22,985 injuries. That is to say, the only two gene manipulated mRNA experimental vaccines, Pfizer-BioNTech and Moderna, accounted for 8,233 deaths of the total registered deaths of 10,570. That’s 78% of all deaths from the four vaccines currently in use in the EU.

And among the serious side effects or injuries recorded by the EMA, for the two mRNA vaccines which we focus on in this article, for the Pfizer “experimental” vaccine, most reported injuries included blood and lymphatic system disorders including deaths; cardiac disorders including deaths; musculoskeletal and connective tissue disorders; respiratory, thoracic and mediastinal disorders, and vascular disorders. For the Moderna mRNA vaccine, most serious injuries or causes of death included blood and lymphatic system disorders; cardiac disorders; musculoskeletal and connective tissue disorders; disorders of the central nervous system.

Note that these are only the most serious injuries related to those two genetically manipulated mRNA vaccines. The EMA also notes that it is believed that only a small percent of actual vaccine deaths or serious side effects, perhaps only 1% to 10%, are reported for various reasons. Officially more than 10,000 persons have died after receiving the coronavirus vaccines since January, 2021 in the EU. That is a horrifying number of vaccine-related deaths, even if the true numbers are far greater.

CDC as well

Even the US Centers for Disease Control (CDC) a notoriously political and corrupt agency with for-profit ties to vaccine makers, in its official Vaccine Adverse Event Reporting System (VAERS), shows a total of 193,000 “adverse events” including 4,057 deaths, 2,475 permanent disabilities, 25,603 emergency room visits, and 11,572 hospitalizations following COVID-19 injections between December 14, 2020 and May 14, 2021. That included the two mRNA vaccines, Pfizer and Moderna, and the far less prevalent J&J Janssen vaccine. Of the reported deaths, 38% occurred in people who became ill within 48 hours of being vaccinated. The official US vaccine-related death toll is greater in just 5 months than all the vaccine-related deaths from the past 20 years combined. Yet the major media worldwide and the US Government virtually bury the alarming facts.

Some 96% of the fatal results were from the Pfizer and Moderna vaccines, the two variants funded and promoted by the Gates Foundation and Tony Fauci’s NIAID with the experimental mRNA genetic technology. Moreover, Dr. Tony Fauci, the US Biden Administration vaccine czar and his NIAID Vaccine Research Center co-designed the Moderna mRNA vaccine and gave Moderna and Pfizer each $6 billion to produce it. That’s also a blatant conflict of interest as Fauci and his NIAID are allowed to financially benefit from their patent earnings in the vaccine under a curious US law. The NIAID developed the coronavirus spike proteins for the development of SARS-CoV-2 mRNA vaccines using taxpayer money. They licensed it to Moderna and Pfizer.

“never seen in nature…”

In a tragic sense, the experience with reactions to the two unprecedented mRNA experimental vaccines since rollout in unprecedented speed “warp speed” as the US Government called it, is only now beginning to be seen, in real trials of human guinea pigs. Few realize that the two mRNA vaccines use genetic manipulations that never before have been used in humans. And under the cover of urgency, US and EU health authorities waived normal animal trials and did not even approve the safety, but gave an “emergency use authorization.” Moreover, the vaccine makers were made 100% exempt from damage litigation.

The general public was reassured of the vaccine safety when Pfizer and Moderna published reports of 94% and 95% “efficacy” of these vaccines. NIAID’s Fauci was quick to call it “extraordinary” in November 2020, and Warp Speed was off and running as was the stock price of Pfizer and Moderna.

Peter Doshi, Associate Editor of the British Medical Journal pointed to a huge flaw in the 90+% reports for efficacy of Moderna and Pfizer vaccines. He noted that the percentages are relative, in relation to the select small healthy young test group, and not absolute as in real life. In real life we want to know how effective the vaccine is among the large general population. Doshi points to the fact that Pfizer excluded over 3400 “suspected COVID-19 cases” that were not included in the interim analysis. Moreover individuals “in both Moderna and Pfizer trials were deemed to be SARS-CoV-1- (the 2003 Asian SARS virus) positive at baseline, despite prior infection being grounds for exclusion,” Doshi notes. Both companies refused to release their raw data. Pfizer in-house scientists did their tests. In short 95% is what Pfizer or Moderna claim. We are told, “Trust us.” A more realistic estimate of the true efficacy of the two vaccines for the general public, using data supplied by the vaccine makers to the FDA, shows the Moderna vaccine at the time of interim analysis demonstrated an absolute risk reduction of 1.1%, while the Pfizer vaccine absolute risk reduction was 0.7%. That is very poor.

Peter Hotez, dean of the National School of Tropical Medicine at Baylor College of Medicine in Houston, says, “Ideally, you want an antiviral vaccine to do two things . . . first, reduce the likelihood you will get severely ill and go to the hospital, and two, prevent infection and therefore interrupt disease transmission.” As Doshi notes, none of the trials were “designed to detect a reduction in any serious outcome such as hospital admissions, use of intensive care, or deaths. Nor are the vaccines being studied to determine whether they can interrupt transmission of the virus.” Moderna’s chief medical officer even admitted that, “Our trial will not demonstrate prevention of transmission.”

Possible effects of mRNA vaccines

In a major new study just published in the International Journal of Vaccine Theory, Practice and Research, Dr. Stephanie Seneff, senior scientist at the MIT Computer Science and Artificial Intelligence Laboratory, and Dr. Greg Nigh, Naturopathic oncology specialist, analyze in detail the possible pathways in which the experimental mRNA vaccines of Pfizer and Moderna could be causing such adverse effects in the vaccinated. First they point out that both the Pfizer and Moderna gene-edited vaccines are highly unstable: “Both are delivered through muscle injection, and both require deep-freeze storage to keep the RNA from breaking down. This is because, unlike double-stranded DNA which is very stable, single-strand RNA products are apt to be damaged or rendered powerless at warm temperatures and must be kept extremely cold to retain their potential efficacy.” Pfizer recommends minus 70’ Celsius.

The authors point out that to keep the mRNA from breaking down before it could produce protein, both vaccine makers substitute methyl-pseudouridine to stabilize RNA against degradation, allowing it to survive long enough to produce adequate amounts of protein antigen. The problem they point out is that, “This form of mRNA delivered in the vaccine is never seen in nature, and therefore has the potential for unknown consequences… manipulation of the code of life could lead to completely unanticipated negative effects, potentially long term or even permanent. ”

PEG Adjuvants and Anaphylactic Shock

For various reasons to avoid using aluminum adjuvants to boost the antibody response, both mRNA vaccines use polyethylene glycol, or PEG, as adjuvant. This has consequences. The authors point out, “…both mRNA vaccines currently deployed against COVID-19 utilize lipid-based nanoparticles as delivery vehicles. The mRNA cargo is placed inside a shell composed of synthetic lipids and cholesterol, along with PEG to stabilize the mRNA molecule against degradation.”

PEG has been shown to produce anaphylactic shock or severe allergenic reactions. In studies of prior non-mRNA vaccines, anaphylactic shock reactions occurred in 2 cases per million vaccinations. With the mRNA vaccines initial monitoring revealed that, “anaphylaxis occurred at a rate of 247 per million vaccinations. This is more than 21 times as many as were initially reported by the CDC. The second injection exposure is likely to cause even larger numbers of anaphylactic reactions.” One study noted, “PEG is a high-risk ’hidden’ allergen, usually unsuspected, and can cause frequent allergic reactions due to inadvertent re-exposure.” Among such reactions are included life-threatening cardiovascular collapse.

This is far from all the undeclared risks of the experimental mRNA coronavirus vaccines.

Antibody-Dependent Enhancement

Antibody-Dependent Enhancement (ADE) is an immunological phenomenon. Seneff and Nigh note that, “ADE is a special case of what can happen when low, non-neutralizing levels of… antibodies against a virus are present at the time of infection. These antibodies might be present due to… prior vaccination against the virus…” The authors suggest that in the case of both Pfizer and Moderna mRNA vaccines, “non-neutralizing antibodies form immune complexes with viral antigens to provoke excessive secretion of pro-inflammatory cytokines, and, in the extreme case, a cytokine storm causing widespread local tissue damage.”

To be clear, normally cytokines are part of the body’s immune response to infection. But their sudden release in large quantities, a cytokine storm, can cause multisystem organ failure and death. Our innate immune system undergoes an uncontrolled and excessive release of pro-inflammatory signaling molecules called cytokines.

The authors add that pre-existing “antibodies, induced by prior vaccination, contribute to severe pulmonary damage by SARS-CoV in macaques…” Another cited study shows that the much more diverse range of prior exposures to coronaviruses such as seasonal flu experienced by the elderly might predispose them to ADE upon exposure to SARS-CoV-2.” This is a possible explanation for the high incidence of post-mRNA vaccination deaths among elderly.

The vaccine makers have a clever way of denial as to the toxicity of their mRNA vaccines. As Seneff and Nigh state, “it is not possible to distinguish an ADE manifestation of disease from a true, non-ADE viral infection.” But they make the telling point, “In this light it is important to recognize that, when diseases and deaths occur shortly after vaccination with an mRNA vaccine, it can never be definitively determined, even with a full investigation, that the vaccine reaction was not a proximal cause. “

The authors make numerous other alarming points including emergence of auto-immune diseases such as Celiac disease, a disease of the digestive system that damages the small intestine and interferes with the absorption of nutrients from food. Also Guillain-Barré syndrome (GBS) that causes progressive muscle weakness and paralysis. Additionally, Immune thrombocytopenia (ITP) in which a person has unusually low levels of platelets — the cells that help blood to clot– could occur following vaccination “through the migration of immune cells carrying a cargo of mRNA nanoparticles via the lymph system into the spleen… ITP appears initially as petechiae or purpura on the skin, and/or bleeding from mucosal surfaces. It has a high risk of fatality through haemorrhaging and stroke.”

These examples are indicative of the fact that we are literally exposing the human race via untested experimental gene edited mRNA vaccines to incalculable dangers which in the end may exceed by far any potential risk of damage from something which has been called SARS-Cov-2. Far from the much-touted miracle substance proclaimed by WHO, Gates, Fauci and others, the Pfizer, Moderna and other possible mRNA vaccines clearly hold potentially tragic and even catastrophic unforeseen consequences. Little wonder some critics believe it is a disguised vehicle for human eugenics.

F. William Engdahl is strategic risk consultant and lecturer, he holds a degree in politics from Princeton University and is a best-selling author on oil and geopolitics, exclusively for the online magazine “New Eastern Outlook”

from:    http://www.williamengdahl.com/englishNEO19May2021.php

Employers Take Note: OSHA

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OSHA: Employers May Be Held Liable for ‘Any Adverse Reaction’ From Mandatory COVID Shots

Matt Agorist May 20

The federal Occupational Safety and Health Administration (OSHA) has issued a rather bombshell update to its website which is not good news to companies who force their employees to take the COVID-19 vaccine. Essentially, according to OSHA, companies may be liable for an employee’s adverse reaction to the vaccine if they require them to take it.

In a recent update to the OSHA website’s FAQ section, the agency outlines the “vaccine related” requirement for on-the-job injuries. In three parts it details the liability.

Are adverse reactions to the COVID-19 vaccine recordable on the OSHA recordkeeping log?

In general, an adverse reaction to the COVID-19 vaccine is recordable if the reaction is: (1) work-related, (2) a new case, and (3) meets one or more of the general recording criteria in 29 CFR 1904.7 (e.g., days away from work, restricted work or transfer to another job, medical treatment beyond first aid).

If I require my employees to take the COVID-19 vaccine as a condition of their employment, are adverse reactions to the vaccine recordable?

If you require your employees to be vaccinated as a condition of employment (i.e., for work-related reasons), then any adverse reaction to the COVID-19 vaccine is work-related. The adverse reaction is recordable if it is a new case under 29 CFR 1904.6 and meets one or more of the general recording criteria in 29 CFR 1904.7.

In a third bullet point, OSHA explicitly notes that employers who do not require their employees to take the vaccine, will not be held liable through the recording criteria in 29 CFR 1904.7. The guideline notes that in order for an employer to be free from liability, the vaccine must be “truly voluntary,” meaning no negative reports for unvaccinated employees.

I do not require my employees to get the COVID-19 vaccine. However, I do recommend that they receive the vaccine and may provide it to them or make arrangements for them to receive it offsite. If an employee has an adverse reaction to the vaccine, am I required to record it?

No. Although adverse reactions to recommended COVID-19 vaccines may be recordable under 29 CFR 1904.4(a) if the reaction is: (1) work-related, (2) a new case, and (3) meets one or more of the general recording criteria in 29 CFR 1904.7, OSHA is exercising its enforcement discretion to only require the recording of adverse effects to required vaccines at this time. Therefore, you do not need to record adverse effects from COVID-19 vaccines that you recommend, but do not require.

Note that for this discretion to apply, the vaccine must be truly voluntary. For example, an employee’s choice to accept or reject the vaccine cannot affect their performance rating or professional advancement. An employee who chooses not to receive the vaccine cannot suffer any repercussions from this choice. If employees are not free to choose whether or not to receive the vaccine without fearing adverse action, then the vaccine is not merely “recommended” and employers should consult the above FAQ regarding COVID-19 vaccines that are a condition of employment.

Note also that the exercise of this discretion is intended only to provide clarity to the public regarding OSHA’s expectations as to the recording of adverse effects during the health emergency; it does not change any of employers’ other responsibilities under OSHA’s recordkeeping regulations or any of OSHA’s interpretations of those regulations.

Finally, note that this answer applies to a variety of scenarios where employers recommend, but do not require vaccines, including where the employer makes the COVID-19 vaccine available to employees at work, where the employer makes arrangements for employees to receive the vaccine at an offsite location (e.g., pharmacy, hospital, local health department, etc.), and where the employer offer the vaccine as part of a voluntary health and wellness program at my workplace. In other words, the method by which employees might receive a recommended vaccine does not matter for the sake of this question.

This clarification by OSHA is especially relevant thanks to the The National Vaccine Injury Compensation Program (NVICP) which removes any and all liability from vaccine manufacturers even if their product kills someone.

You can actually prove that you or your child were harmed from a vaccine yet the vaccine maker is completely shielded from liability. Even if you are awarded monetary compensation through the NVICP, the taxpayers are put on the line, not the vaccine makers.

If companies have to start footing the bill for lawsuits related to COVID-19 vaccine adverse reactions, the implications for vaccine manufacturers could be massive especially given the sheer magnitude of adverse events being reported to the CDC from the COVID-19 vaccine.

The most recent data released by the Centers for Disease Control and Prevention (CDC) on the number of injuries and deaths reported to the Vaccine Adverse Event Reporting System (VAERS) following COVID vaccines reveals there have been over 192,954 adverse events reported. Of those adverse reactions, according to the CDC, 17,190 consist of serious injuries, and 4,434 of them are deaths — up nearly 300 deaths, 30,000 adverse events, and 1,000 serious adverse events since we reported on it last week.

from:    https://thefreethoughtproject.com/osha-adverse-reaction-reporting/

Pay No Attention to he Facts

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Facebook Labeling 100% Facts About Vaccine Company Corruption as ‘Misinformation’

Don Via Jr. May 18, 2021

The censors at Facebook’s ministry of truth have sunk to a new low. Yesterday at 1:35 p.m. EST, TFTP journalist Don Via Jr received a 24-hour ban on the platform for posting a completely factually accurate meme acknowledging big pharma’s history of rampant corruption.

Unlike other instances of individuals being censored on the platform however, in which the social media company attempts to thinly veil their censorship behind openly biased fact-checkers. This time there was none. No “fact check” for “false information”. Simply a notification of the post being removed from Mr. Via’s Break The Matrix Facebook page, and a notice that all of his accounts were restricted for 24 hours.

Below is the meme in question.

What makes this act of censorship particularly egregious is the blatant nature with which Facebook is now suppressing 100% verifiable facts.

After disputing the decision, Facebook replied with an automated message stating “We don’t allow false information that could cause physical harm. In some cases this includes information that recognized health organizations say could mislead people about how to cure or prevent a disease or that could discourage people from seeking medical treatment.”

In this case though, none of the information stated was false.

For instance, the first tier of the graphic claims that since inception in 1848, Pfizer has racked up nearly 5 billion dollars in criminal charges. While the exact total may vary a bit, the facts regarding their history of rampant corruption and medical malfeasance is.

In 1991, the FDA charged Pfizer subsidiary Shiley with withholding information from safety regulators and deliberately falsifying manufacturing records with regards to faulty heart valves. Nearly 300 people died from Pfizer’s faulty products and ultimately the company spent 205 million dollars settling the tens of thousands of lawsuits filed against them.

Despite this, Pfizer resisted to comply with FDA orders to notify patients and ultimately paid an additional $10 million when the Department of Justice charged them with lying to regulators.

In 2009, among other allegations of human rights abuses, Pfizer agreed to settle a lawsuit for $75 million after a lengthy court dispute in which it was charged with using Nigerian children as human guinea pigs.

In 2012 the company was forced to pay 60 million dollars after it was exposed for bribing foreign doctors to sell their products.

These are only a select few examples of the company’s history rife with criminal activity. More can be seen under Pfizer’s corporate rap sheet via the Corporate Research Project.

The second tier of the meme asserts that Moderna has not successfully completed the production of a viable vaccine in the company’s history. This can be confirmed via a simple internet search. In May of 2020, it was reported by The Daily Mail and CNN that Moderna has a track record of never bringing a successful vaccine to market since the company’s founding in 2010.

Furthermore, despite the company’s dubious past it was reported that Moderna was first tapped to lead U.S. vaccine development in what equated to a gamble. Simply because the company’s slick talking CEO was able to get the attention of former President Trump with bold promises during a meeting with biotech executives.

The third tier of the meme acknowledges the well-documented history of heinous crimes committed by Johnson & Johnson. Of which TFTP has also extensively covered in recent years.

As we reported in 2016, the company was forced to pay out billions of dollars in several lawsuits for continuing the sale of products they knew were causing cancer.

J&J has also been found guilty of irresponsible marketing practices and penalized nearly 600 million dollars for their role in fueling the opiate epidemic. As well as having been caught hiding crucial laboratory data from safety inspectors — resulting in the deaths of hundreds of people.

But these only scratch the surface of the company’s flagrant human rights abuses. Among them, being one of the main financiers alongside, Dow Chemical and the United States Army, funding 20 years of unethical human experiments by Dr. Albert Kligman in Pennsylvania’s Holmesburg prison. Experiments which entailed prisoners being financially coerced to “volunteer” as research subjects to study mind-altering drugs, painful medical procedures, radiation, and chemical weapons such as Agent Orange.

As a matter of fact, in addition to Pfizer and Johnson & Johnson — It is thoroughly documented by the Corporate Research Project that nearly every major company involved in the development of Covid-19 vaccines has an abhorrent history of medical malfeasance, and criminal charges.

Finally, the last section of the meme asserts that AstraZeneca’s covid-19 vaccine has itself already been suspended in 24 countries due to health concerns. Yet again, a simple query in your preferred search engine can corroborate this as a fact.

As a March 16th report from Al Jazeera explains; the countries of Sweden, Latvia, France, Germany, Italy, Spain, Luxembourg, Cyprus, Portugal, Slovenia, Indonesia, the Netherlands, Ireland, Bulgaria, the Democratic Republic of Congo, Thailand, Romania, Iceland, Denmark, Norway, and Austria have all suspended the Oxford / AstraZeneca jab in some capacity.

Since that report the Philippines and Australia have also suspended the shot for individuals under 60 years of age. Venezuela has also refused to authorize it.

What Facebook is doing by deleting this content, which by all accounts is completely accurate, is suppressing vital information that the people have a right to know. Informed consent matters, and it’s not something that can be so freely thrown to the wayside — certainly not as adverse events reported to the CDC are at an all-time high.

Facebook, as we have reported ad nauseam, works alongside government entities to facilitate their censorship. And more recently was even implicated in a lawsuit filed by Robert F Kennedy Jr as directly taking orders from the government to stifle concerns for vaccine safety on its platform.

The company is now essentially working as a cover-up crew to protect those with which they have a vested financial or political interest. While their counterparts in the mainstream media ingloriously propagate the notion that those concerned with vaccine safety are domestic terrorists.

Bodily autonomy is paramount, and individuals have an inherent right to be given all the facts so that they are adequately informed to make proper decisions with regard to their health.

Just because the truth is unpleasant, does not make it misinformation. As a matter of fact, censoring unpleasant truths in favor of biased one-sided narratives is the greatest danger of all.

from:   https://thefreethoughtproject.com/facebook-labeling-100-facts-about-vaccine-company-corruption-as-misinformation/

Who’s Not Trusting the Science Now?

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Dr. Fauci Can’t Explain Why Texas COVID Cases Keep Dropping Despite Reopening

by Tyler Durden
Wednesday, Apr 07, 2021 – 04:01 AM

More than a month has passed since Texas Gov. Greg Abbott shocked the Faucis of the world by scrapping COVID-inspired restrictions on businesses and individuals, including removing the mask mandate. The decisions prompted Dr. Anthony Fauci and legions of public health “experts” to warn about the devastating consequences – thousands of unnecessary deaths would result, they said – however, as the data show, practically every metric has shown that the Lone Star State’s outbreak has continued to recede, even as blue states like Michigan are seeing a new surge in infections (believed to be driven by “mutant” strains).

As epidemiologists everywhere have struggled to come up with an explanation, it’s worth noting that Texans are dining out more, according to Opentable seatings, which have become a closely watched proxy for post-quarantine economic activity.

As experts have struggled to come up with a satisfying answer, Dr. Fauci was asked about the phenomenon during an interview on MSNBC Tuesday morning as the senior advisor to President Biden made the rounds. As MSNBC noted, “if you go to Texas…it looks like 2019… the restaurants are full…the ballparks are full…” and yet, cases have continued to tick downward.

Dr. Fauci seemed dumbfounded. He first suggested that the surge in cases simply hadn’t manifested yet because of a “lag”. That might have made sense if the trend had only been in place for a week or two. But a month has passed, and Texas’ positivity rate – the share of new tests that yield positive results, seen as a more accurate representation of community spread – has continued to fall.

“It can be confusing because you may see a lag or a delay, because often you have to wait a few weeks…there’s a lot of things that go into that,” Dr. Fauci said.

“I’m not really sure, it could be because they’re doing things outdoors, you know it’s very difficult to just one-on-one compare that…I hope they continue to tick down, if they do that would be great. But there’s always the concern that when you pull back on methods, particularly things like indoor dining, or bars that are crowded…you could see a delay, then all of a sudden cases tick back up.”

“We’ve been fooled before with places opening up, then nothing happens, but all of a sudden a few weeks later cases explode on you.”

He concluded by saying “we’ve got to be careful we don’t prematurely judge” the situation in Texas.

For those who haven’t been closely following the situation in Texas, 26 days have passed since the state “reopened 100%” with no mask mandate, and 34 days have passed since Gov. Abbott announced the reopening. The number of new cases, deaths, hospitalizations ICU occupancy and positivity rate have all fallen.

Source: NYT

The doctor then speculated that last night’s packed Texas Rangers game might be a “super-spreader event” (like Sturgis? … or The Super Bowl party in Miami?).

Dr. Fauci has already rejected the CDC Director Walensky’s “impending doom” rhetoric, and on Tuesday, he told CNBC that “as long as we keep vaccinating people efficiently and effectively, I don’t think [a fourth wave] is gonna happen.”

However, “that doesn’t mean we’re not going to still see an increase in cases.”

Meanwhile, the White House announced Tuesday that it’s moving up its target date for all American adults to be eligible to receive a vaccine to April 19, two weeks earlier than its prior stated goal. Already, the government has doled out nearly 150M doses.

from:    https://www.zerohedge.com/covid-19/dr-fauci-cant-explain-why-texas-covid-cases-keep-dropping-despite-reopening?utm_campaign=&utm_content=Zerohedge%3A+The+Durden+Dispatch&utm_medium=email&utm_source=zh_newsletter

Moving Mummies

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Egypt parades 22 mummies through Cairo, showing off ancient heritage & putting ‘Pharaoh’s curse’ myth to rest (PHOTOS, VIDEO)

4 Apr, 2021 04:55 / Updated 1 day ago

Egypt parades 22 mummies through Cairo, showing off ancient heritage & putting ‘Pharaoh’s curse’ myth to rest (PHOTOS, VIDEO)
Royal mummies are transported in a convoy from the Egyptian Museum in Tahrir to the National Museum of Egyptian Civilization in Fustat, in Cairo, Egypt, April 3, 2021 ©  Reuters / Amr Abdallah Dalsh
Egypt has relocated its ancient kings and queens, including Ramses II and Hatshepsut, one of the few known female pharaohs, to a new resting place in a grand ceremony designed to showcase the country’s heritage and boost tourism.

The convoy of golden trucks that moved through the streets of Cairo on Saturday was designed to resemble the ancient boats that once carried deceased pharaohs to their tombs.

RT
The mummy of King Ramesses V ©  Reuters / Amr Abdallah Dalsh

The mummies were transported inside climate-controlled capsules filled with nitrogen from the Egyptian Museum to the newly-inaugurated National Museum of Egyptian Civilization in a spectacular ceremony.

As the mummies made the one-hour journey to their new resting place in Fustat, the site of Egypt’s first Islamic capital, the historic event was widely broadcast on TV and online.

RT
Egyptian artists perform near pyramids at a ceremony of a transfer of Royal mummies ©  Reuters TV

The show featured various artistic performances and famous landmarks in an apparent bid to boost tourism, which has stalled during the Covid-19 pandemic.

RT
©  Reuters TV

As the procession circled Cairo’s Tahrir Square, an obelisk surrounded by four sphinxes was officially unveiled in the square.

RT
A light display in Tahrir Square in Cairo, Egypt, April 3, 2021 ©  Reuters / Mohamed Abd El Ghany

President Abdel Fattah al-Sisi, as well as the heads of UNESCO and the World Tourism Organization, welcomed the mummies at their new home, where Egyptologists say they will now be displayed in a more “civilized” and “educated”manner.

RT
General view of a parade at a ceremony of a transfer of Royal mummies from the Egyptian Museum in Tahrir to the National Museum of Egyptian Civilization in Fustat, in Cairo, Egypt April 3, 2021, ©  Reuters TV

In recent weeks, Egypt has experienced a series of unfortunate incidents – including the Suez Canal blockage, a fatal train crash, a garment factory fire, and a deadly apartment building collapse – reanimating the ‘pharaoh’s curse’ myth. However, with the 18 ancient kings and four queens now finally settled in their new home, perhaps that myth can also be put to rest at last.

from:   https://www.rt.com/news/520071-egypt-pharaoh-mummies-parade/

What’s In Your Water?

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Groundbreaking Investigation Finds Alarming Levels of Arsenic, Lead and Toxic Chemicals in U.S. Tap Water

A joint investigation by the Guardian and Consumer Reports found drinking water samples from systems servicing more than 19 million people in the U.S. contained unsafe levels of multiple contaminants.

Millions of people face serious water quality problems in the U.S.

On Tuesday, the Guardian released the results of a nine-month investigation conducted jointly with Consumer Reports (CR) which showed alarming levels of heavy metals like arsenic, lead and chemicals from plastic PFAS (per- and polyfluoroalkyl substances) in drinking water samples across the U.S.

According to the Guardian, millions of people face serious water quality problems in the U.S. because of contamination, deteriorating infrastructure and inadequate treatment at water plants.

As part of the study, CR and the Guardian selected 120 volunteers to provide tap water samples which were then tested for heavy metals like lead and arsenic, contaminants and PFAS — a group of compounds found in hundreds of household products that are linked to learning delays in children, cancer and other health problems.

The samples came from water systems that service more than 19 million people.

Here are four key findings from this report:

  • A total of 118 of 120 samples analyzed had concerning levels of PFAS, arsenic or lead exceeding safety thresholds set by CR scientists and other health experts.
  • Almost every sample had measurable levels of PFAS and more than 35% of samples contained the potentially toxic “forever chemicals,” at levels that exceeded CR’s  maximum safety threshold.
  • About 8% of samples contained arsenic at levels above CR’s recommended maximum.
  • One tested water sample in New Britain, Connecticut, had a lead concentration of 31.2 ppb — more than double the U.S. Environmental Protection Agency’s (EPA) action level of 15 ppb, and 25 ppb higher than the water quality report sent to people who use the water.

In response to the findings, EPA spokesperson Andrea Drinkard said 93% of the population supplied by community water systems get water that meets “all health-based standards all of the time” and that the agency has set standards for more than 90 contaminants. That includes arsenic and lead but not PFAS.

However, according to an analysis of more than 140,000 public water systems published by the Guardian in February, millions of people in the U.S. are drinking water that fails to meet federal health standards, including limits for dangerous contaminants.

‘Forever chemicals’ (PFAS) in tap water

CR’s results showed PFAS in 117 of 120 samples tested, from locations across the country. Two CR samples had PFAS levels above the federal advisory level of 70 ppt, with the highest amount at 80.2 ppt.

PFAS chemicals have been manufactured and used in a variety of industries in the U.S. since the 1940s, according to the EPA. They can be found in food packaging, commercial household products, stain and water-repellent fabrics, nonstick cookware, polishes, waxes, paints, cleaning products, fire-fighting foams, oil and plastics industries and contaminated drinking water.

PFAS chemicals seep into water from factories, landfills and other sources. They’re often called “forever chemicals” because they can accumulate in the body and don’t easily break down in the environment.

An investigation into the health effects of PFAS involving research of 69,000 people revealed a “probable link” between exposure to a type of PFAS chemical and six health problems: high cholesterol, ulcerative colitis, thyroid disease, pregnancy-induced hypertension, and testicular and kidney cancers. Research has also linked PFAS to learning delays in children.

As reported by The Defender, science suggests links between PFAS exposure and a range of health consequences, including possible increased risks of cancer, thyroid disease, high cholesterol, liver damage, kidney disease, low birth-weight babies, immune suppression, ulcerative colitis and pregnancy-induced hypertension.

At least 2,337 communities in 49 states have drinking water known to be contaminated with PFAS, according to a January analysis by the Environmental Working Group, an advocacy organization.

Despite evidence of widespread contamination and health risks, the EPA has not set an enforceable legal limit for PFAS in drinking water. It has established only voluntary limits, which apply to just two forever chemicals — perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS) — at 70 parts per trillion combined.

Harvard environmental health professor Philippe Grandjean has suggested that the limit should be just 1 ppt for PFOA and PFOS, citing his 2013 research published in Environmental Health.

Most municipalities don’t test for PFAS, and when they do, it’s only on a small scale.

Toxic arsenic in tap water

Almost every sample CR tested had measurable levels of arsenic, a common groundwater contaminant, including 10 samples with levels between 3 and 10 ppb, according to the Guardian.

CR scientists and environmental advocacy groups like the Natural Resources Defense Council (NRDC) have said the limit should be 3 ppb or lower, but the EPA allows arsenic in drinking water up to 10 ppb to balance the costs for water system operators against reducing health risks.

Research suggests exposure to minimal levels of arsenic can pose long-term health risks. A 2014 study in Environmental Health found that arsenic at 5ppb or greater was associated with reduced IQ in children.

As The Defender reported in March, arsenic was “ranked number one among substances present in the environment that pose the most significant potential threat to human health,” according to a congressional report that resulted from an investigation into heavy metals like lead and arsenic found in baby food.

According to the report: “Exposure to toxic heavy metals causes permanent decreases in IQ, diminished future economic productivity, and increased risk of future criminal and antisocial behavior in children. Toxic heavy metals endanger infant neurological development and long-term brain function.”

Dangerous level of lead in tap water

Concerns of lead in drinking water first made national headlines during the Flint, Michigan water crisis in 2015. Scientists and the EPA have agreed there is no safe exposure level for lead, though the EPA’s action level for lead is set at 15 ppb.

While New Britain’s annual water quality report for customers indicated that its average lead level was 6 ppb, one sample tested by CR showed lead concentrations of 31.2 ppb, more than double the EPA’s action level of 15 ppb.

Lead typically works its way into drinking water through lead pipes leading to peoples’ homes or in the homes’ plumbing. An estimated 3 to 6 million homes and businesses in the U.S. still get water through older lines that contain lead, according to EPA estimates, and an unknown number of homes have plumbing fixtures made of the heavy metal.

It is well established that inorganic arsenic and lead found in tap water are neurotoxic and can result in reduced IQ as well as adverse neurodevelopmental outcomes, such as autism spectrum disorder and attention-deficit/hyperactivity disorder (ADHD) — two conditions that have been steadily climbing for several decades, reported The Defender.

According to the Agency for Toxic Substances and Disease Registry, lead can also cause reproductive issues, low bone density, poor kidney function, cognitive decline and negatively impacts every organ system in the body. High levels of exposure can cause encephalopathy or death.

The American Academy of Pediatrics has identified no “threshold or safe level of lead in blood.”

Next steps — solving the problem

Although people can seek cleaner drinking water by using filters and home filtration systems that remove dangerous contaminates, CR says fixing the problem shouldn’t be up to consumers.

The NRDC has called on the Biden administration and Congress to enact legislation requiring the expeditious removal and replacement of lead lines and to take immediate steps to address PFAS contamination in drinking water.

from:    https://childrenshealthdefense.org/defender/arsenic-lead-toxic-chemicals-tap-water/?utm_source=salsa&eType=EmailBlastContent&eId=8a2338f9-c91c-4d41-816c-8533cf90d2d8

Cutting Through the Rhetoric

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“We’re So Stupid Following Our Politicians” – Charles Barkley Unleashes One Minute Of Truth On America

by Tyler Durden
Monday, Apr 05, 2021 – 05:44 AM

Forget Orwell’s “Two Minutes Hate.” NBA legend Charles Barkley unleashed ‘One Minute Truth’ on NCAA-Final-Four-watchers last night, telling viewers that:

“I truly believe in my heart most white people and black people are awesome people, but we’re so stupid following our politicians, whether they’re Republicans or Democrats.”

Barkley was responding to a feature that detailed how on April 4, 1968, Robert F. Kennedy broke the news about the assassination of Martin Luther King Jr. to a crowd in Indianapolis, urging people to seek compassion and justice rather than anger and revenge, saying the vast majority of Americans, both black and white, want to live in peace with each other.

As a reminder, Robert F. Kennedy was assassinated two months later.

This was the same message Barkley offered, as he warned:

“I think our system is set up where our politicians, whether they’re Republicans or Democrats, are designed to make us not like each other so they can keep their grasp of money and power.”

Furthermore, he described what he believes to be the thinking behind the divide-and-conquer strategy:

 “Hey, let’s make these people not like each other. We don’t live in their neighborhoods, we all got money, let’s make the whites and blacks not like each other, let’s make rich people and poor people not like each other, let’s scramble the middle class.”

Watch the full clip here:

This is not the first time Barkley has unleashed uncomfortable truths. In September of last year he dared to speak common sense against the left’s calls to defund the police, arguing that poor black communities would be hit hardest by a spike in crime if there is less policing. “Who are black people supposed to call, Ghostbusters, when we have crime in our neighborhood?”

How long will it be before the outrage mob comes for Barkley for taking such a “bothist” common-sense and honest view and refusing to be drawn, like weak CEOs or pandering politicians to one side or the other in our ever more divisive society?

It’s already begun…

…sigh

from:    https://www.zerohedge.com/political/were-so-stupid-following-our-politicians-charles-barkley-unleashes-one-minute-truth?utm_campaign=&utm_content=Zerohedge%3A+The+Durden+Dispatch&utm_medium=email&utm_source=zh_newsletter

eDNA and Implications

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Scientists Collect Animal DNA From Air For the First Time Ever

The practice could help better understand the transmission of diseases such as COVID-19.

By 

Apr 02, 2021

Scientists Collect Animal DNA From Air For the First Time Ever
ktsimage/iStock

For the first time ever, scientists have managed to collect environmental DNA (eDNA) from the air. The practice, still at its early stages, could revolutionize forensics, anthropology, and even medicine.

The scientists first took air samples from a room that had housed naked mole-rats and showed that airDNA sampling could successfully detect mole-rat DNA within the animal’s housing. The scientists also spotted human DNA in the air samples.

They initially ventured a guess that this might be due to contamination. However, with further research, they came to the conclusion that the human genetic material was moving away from its original source and spreading throughout the air.

“The use of eDNA (environmental DNA) has become a topic of increasing interest within the scientific community particularly for ecologists or conservationists looking for efficient and non-invasive ways to monitor biological environments. Here we provide the first published evidence to show that animal eDNA can be collected from air, opening up further opportunities for investigating animal communities in hard to reach environments such as caves and burrows,” Dr. Elizabeth Clare, Senior Lecturer at Queen Mary University of London and first author of the study, said.

The researchers are now working with partners in the industry to bring some of the potential applications of this technology to life. Clare added that: “What started off as an attempt to see if this approach could be used for ecological assessments has now become much more.”

Clare further explained that the technique could help researchers to better understand the transmission of airborne diseases such as COVID-19. “At the moment social distancing guidelines are based on physics and estimates of how far away virus particles can move, but with this technique we could actually sample the air and collect real-world evidence to support such guidelines,” Clare explained.

The study is published in the journal PeerJ.

from:    https://interestingengineering.com/scientists-collect-animal-dna-from-air-for-the-first-time-ever?fbclid=IwAR0X37Y2EfL_rHh3zyiCM20AqWWX3Y45m_pxwOmJKcDgRwTTOj2S9kHq-tw

Question

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Re: Do doctors have to have the covid-19 vaccine?

02 April 2021
K Polyakova   Consultant    London

Dear Editor

I have had more vaccines in my life than most people and come from a place of significant personal and professional experience in relation to this pandemic, having managed a service during the first 2 waves and all the contingencies that go with that.

Nevertheless, what I am currently struggling with is the failure to report the reality of the morbidity caused by our current vaccination program within the health service and staff population. The levels of sickness after vaccination is unprecedented and staff are getting very sick and some with neurological symptoms which is having a huge impact on the health service function. Even the young and healthy are off for days, some for weeks, and some requiring medical treatment. Whole teams are being taken out as they went to get vaccinated together.

Mandatory vaccination in this instance is stupid, unethical and irresponsible when it comes to protecting our staff and public health. We are in the voluntary phase of vaccination, and encouraging staff to take an unlicensed product that is impacting on their immediate health, and I have direct experience of staff contracting Covid AFTER vaccination and probably transmitting it. In fact, it is clearly stated that these vaccine products do not offer immunity or stop transmission. In which case why are we doing it? There is no longitudinal safety data (a couple of months of trial data at best) available and these products are only under emergency licensing. What is to say that there are no longitudinal adverse effects that we may face that may put the entire health sector at risk?

Flu is a massive annual killer, it inundates the health system, it kills young people, the old the comorbid, and yet people can chose whether or not they have that vaccine (which had been around for a long time). And you can list a whole number of other examples of vaccines that are not mandatory and yet they protect against diseases of higher consequence.

Coercion and mandating medical treatments on our staff, of members of the public especially when treatments are still in the experimental phase, are firmly in the realms of a totalitarian Nazi dystopia and fall far outside of our ethical values as the guardians of health.

I and my entire family have had COVID. This as well as most of my friends, relatives and colleagues. I have recently lost a relatively young family member with comorbidities to heart failure, resulting from the pneumonia caused by Covid. Despite this, I would never debase myself and agree, that we should abandon our liberal principles and the international stance on bodily sovereignty, free informed choice and human rights and support unprecedented coercion of professionals, patients and people to have experimental treatments with limited safety data. This and the policies that go with this are more of a danger to our society than anything else we have faced over the last year.

What has happened to “my body my choice?” What has happened to scientific and open debate? If I don’t prescribe an antibiotic to a patient who doesn’t need it as they are healthy, am I anti-antibiotics? Or an antibiotic-denier? Is it not time that people truly thought about what is happening to us and where all of this is taking us?

Competing interests: No competing interests

from:    https://www.bmj.com/content/372/bmj.n810/rr-14

Honestly, It’s Perfectly Safe!

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Number of COVID Vaccine Injuries Reported to VAERS Surpasses 50,000, CDC Data Show

VAERS data released today showed 50,861 reports of adverse events following COVID vaccines, including 2,249 deaths and 7,726 serious injuries between Dec. 14, 2020 and March 26, 2021.

Every Friday, VAERS makes public all vaccine injury reports received to the system as of Friday of the previous week.

Data released today by the Centers for Disease Control and Prevention (CDC) on the number of injuries and deaths reported to the Vaccine Adverse Event Reporting System (VAERS) following COVID vaccines revealed steadily rising numbers, but no new trends. VAERS is the primary mechanism for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.

Every Friday, VAERS makes public all vaccine injury reports received to the system as of Friday of the previous week. Today’s data show that between Dec. 14, 2020, and March 26, a total of 50,861 total adverse events were reported to VAERS, including 2,249 deaths — an increase of 199 over the previous seven days — and 7,726 serious injuries, up 631 over the same time period.

Of the 2,249 deaths reported as of March 26, 28% occurred within 48 hours of vaccination, 19% occurred within 24 hours and 43% occurred in people who became ill within 48 hours of being vaccinated.

In the U.S., 136.7 million COVID vaccine doses had been administered as of March 26.

From the 3-26-2021 release of VAERS data.

This week’s VAERS data show:

  • 19% of deaths were related to cardiac disorders.
  • 45% of those who died were male, 43% were female and the remaining death reports did not include gender of the deceased.
  • The average age of those who died was 77.7 and the youngest death was an 18-year-old.
  • As of March 26, 341 pregnant women had reported adverse events related to COVID vaccines, including 104 reports of miscarriage or premature birth.
  • Of the 578 cases of Bell’s Palsy reported, 63% of cases were reported after Pfizer-BioNTech vaccinations — almost twice as many as reported (36%) following vaccination with the Moderna vaccine. Seven cases of Bell’s Palsy were reported with Johnson & Johnson (J&J) vaccine (1%).
  • There were 2,578 reports of anaphylaxis, with 53% of cases attributed to the Pfizer-BioNTech vaccine, 44% to Moderna and 3% to J&J vaccine, which was rolled out in the U.S. on March 2.
  • Using a broadened search for any reference to anaphylaxis in chart notes resulted in 15,193 reports, with 52% of cases attributed to Pfizer’s COVID vaccine, 45% to Moderna and 3% to J&J. With each vaccine, nearly 42% of anaphylactic reports occurred in people aged 17-44.

According to the CDC’s website, “the CDC follows up on any report of death to request additional information and learn more about what occurred and to determine whether the death was a result of the vaccine or unrelated.”

Ask Congress to Investigate COVID Origins – Take Action

To date, the only information the CDC has published related to the investigation of COVID vaccine-related deaths and how those investigations were conducted is a COVID-19 Vaccine Safety Update via the Advisory Committee on Immunization Practices, published Jan. 27.

An interview in MedPage Today highlighted the shortfalls of the post-marketing surveillance of the COVID vaccine. Aaron Kesselheim, professor of medicine at Harvard Medical School and Brigham and Women’s Hospital in Boston, said we are seeing a lot of spontaneous reporting, a lack of formal post-approval studies because vaccines have only received Emergency Use Authorization and vaccines being given outside the healthcare systems — interfering with the ability to rigorously collect observational data.

Although the CDC and U.S. Food and Drug Administration (FDA) have various systems in place to monitor the safety of vaccines, they are not “up and running” and do not have adequate resources behind them, Kesselheim said.

According to Kesselheim, there’s essentially nobody keeping track of COVID adverse reactions in the U.S. and no long-term safety data, but emphasized that this new mRNA technology is “extremely effective and extremely safe.”

On March 8, The Defender contacted the CDC with questions about reported deaths and injuries related to COVID vaccines. We provided a written list of questions about how the CDC conducts investigations into reported deaths, the status of investigations on deaths reported in the media, if autopsies are being done and the standard for determining whether an injury is causally connected to a vaccine.

We also inquired about whether healthcare providers are reporting all injuries and deaths that might be connected to the COVID vaccine, and what education initiatives are in place to encourage and facilitate proper and accurate reporting.

It took the CDC 22 days to respond to our repeated inquiries. When someone did, the person told us the agency had never received the questions — even though the employees we talked to several times said their press officers were working through the list of questions and were reviewing the email we sent. We provided the questions again yesterday, and requested a response by April 7.

Breakthrough cases

On March 31, The Defender reported on the increasing number of “breakthrough cases” of COVID in fully vaccinated people. Washington, Florida, South Carolina, Texas, New York, California and Minnesota have all reported breakthrough cases of COVID, some of which have resulted in hospitalization and death. Investigations are underway to determine if there were problems with the vaccines or if people had been infected with a variant.

When asked about the increasing number of breakthrough cases during a White House press conference, Dr. Anthony Fauci, President Biden’s chief medical advisor, said it is something they will take seriously and follow closely, but breakthrough infections happen with any vaccination.

CDC issues new travel guidance, vaccine passports stir controversyThe CDC today issued new travel guidance stating that fully vaccinated Americans traveling within the U.S. do not have to get tested for COVID before or after their trip, and do not need to self-quarantine when they return home.

On March 29, The Defender reported that the Biden administration and private companies are working to develop vaccine passports that would require Americans to prove they’ve been vaccinated against COVID as the country opens.

Dr. Naomi Wolf, founder and CEO of Daily Clout, said the passport system really isn’t about the vaccine. It’s about your data, and “once this rolls out you don’t have a choice about being part of the system.”

Rep. Pete Sessions (R-Texas) said that vaccine credentials are a complete government overstep that will undermine public trust and substantially limit normal day-to-day essential activities. Rep. Lauren Boebert (R-Colo.) said “vaccine passports are unconstitutional. Period.”

On March 26, New York launched a digital vaccine passport system known as Excelsior Pass that residents can use to prove they’ve been vaccinated or recently tested negative for infection. The New York system, built on IBM’s digital health pass platform, will be used at dozens of events, including arts and entertainment venues.

J&J  makes headlines with manufacturing mix-up, report of severe allergic reaction

As The Defender reported April 1, 15 million doses of J&J’s vaccine failed quality control after workers at a Baltimore manufacturing plant negligently put an AstraZeneca ingredient in J&J’s COVID vaccine. The mix-up forced regulators to delay authorization of the plant’s production lines and prompted an investigation by the FDA.

On March 31, Business Insider reported that a 74-year-old Virginia man suffered a rare reaction to J&J’s vaccine that caused a painful rash to spread across his entire body and skin to peel off. Richard Terrell told local news station WRIC he began suffering strange symptoms four days after receiving the vaccine.

“I began to feel a little discomfort in my armpit and then a few days later I began to get an itchy rash, and then after that I began to swell and my skin turned red,” Terrell said.

The rash spread to his entire body and his skin peeled off. He went to the emergency room, where doctors determined that he had experienced an adverse reaction to the COVID vaccine.

AstraZeneca suspended in Germany and Canada 

On March 31, The Defender reported that Germany indefinitely suspended use of the Oxford-AstraZeneca COVID vaccine for anyone under 60 following advice from STIKO, the country’s independent vaccine committee and external experts.

The committee investigated reports of blood clots, some fatal, in people who received the vaccine and decided to give the vaccine only to people 60 or older unless they belong to a high-risk category where the benefits outweigh the risk of a serious side-effect.

As The Defender reported on March 30, several regions of Germany, including Berlin and Munich, had temporarily paused the vaccine for people under 60 after Germany’s vaccine regulator disclosed 31 cases of a rare brain blood clot, nine of which resulted in deaths. The decision was made as a precaution ahead of a meeting with national medical regulators scheduled for later in the day where it was decided to indefinitely suspend the vaccine.

On March 30, Canada announced it was suspending AstraZeneca’s vaccine for people under age 55 following concerns it might be linked to rare blood clots, The Defender reported.

Health Canada demanded AstraZeneca conduct a detailed study on the risks and benefits of its COVID vaccine across multiple age groups, and suspended the vaccine for younger groups pending the outcome of that review.

On March 24, Health Canada updated the product information for AstraZeneca’s COVID vaccines to warn of the risk of rare blood clots associated with low levels of blood platelets following vaccinations — a stark reversal from Canada’s former position.

Children’s Health Defense asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.

from:    https://childrenshealthdefense.org/defender/covid-vaccine-injuries-vaers-cdc/?utm_source=salsa&eType=EmailBlastContent&eId=9af36675-e8d3-4040-a6be-abcb46990996