Archive for the ‘vaccines’ Category

The Bear Metaphor & Your DNA

https://naomiwolf.substack.com/p/facing-the-beast

Facing the Beast

Can We Really Confront the Biggest Crime in Human History?

Dr Naomi Wolf
Excerpts:

I was relaxing in our screened porch in our little cottage in the forest, feeling rather pleased with myself. It had been an arduous week of the usual combat for liberty, but there had been victories.

Then I heard a “thump” about eight feet away behind my head.

I glanced behind me and saw the enormous ears and forehead of a sizable brown bear, who was ducking insolently, clearly aware of me, to lower himself behind the trash cans.

My heart pounded as I realized that he was not leaving; he continued pacing and circling, no matter where I went.

He was here because — I had done nothing to stop him. He was here because I let him slowly take over our home.

This all, of course, really happened. But that does not mean it is not also a metaphor.

The same week that this happened, I also finalized my reporting about the Pfizer vaccines, showing — what I knew for months I would eventually find.

The heart of the manufacture and distribution of millions of doses of the MRNA vaccines that are causing such a swath of death and destruction throughout North America and Western Europe, is enmeshed with the plans, methods and manufacturing infrastructure of our existential adversary.

The enemy is within our very bodies.

(See link for article)

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SUMMARY:

  • Wolf believes this isn’t just about a greedy pharmaceutical company and a corrupt regulatory agency but a massive act of war.
    • Doubling of neonatal deaths, 34% above normal stillbirths and spontaneous abortions for “vaxxed” moms
    • 40% increase in death rates, shocking rise in disability
  • 2021 Hong Kong study (answerable to the CCP) showed when mice got the second dose of the booster, it resulted in visibly enlarged hearts with white patches, cytokine storms and liver damage seen by the naked eye.  The study concluded: “Post-vaccination myopericarditis is reported after immunization with coronavirus disease 2019 (COVID-19) messenger RNA (mRNA) vaccines.” 

  • Pfizer/BioNTech is a German-Chinese company and has an MOU with Fosun Pharmaceuticals, a major CCP-linked pharmaceutical company based in Shanghai, to make the Pfizer/BioNTech MRNA “vaccines”.  A SEC filing shows that the MOU with Fosun includes an equity investment by Fosun in BioNTech. In other words, the CCP is an equity investor in BioNTech.  Fosun is not separate from the CCP; it is the CCP.
  • Fosun Pharma did not stay in China.  It came here. Fosun Pharmaceuticals is now also Fosun Pharmaceuticals USA, with branches for R and D and product formulation in Boston, MA and Princeton, NJ.
    • Fosun produces products in the US for distribution here and around the world and has has built a “global operation strategy” for the manufacture of COVID-19 vaccines, COVID-19 PCR tests and COVID-19 antigen tests. (These tests were the primary metric that determined the ‘pandemic’ and thus the lock downs. So a CCP-run company, and a CCP product decides who can go to work, school, and travel.)
    • A lawsuit has been filed in NY surrounding COVID testing because commercial labs get DNA, which then goes to Fulgent Genetics, which states they’re going to destroy all the samples and that they aren’t selling them to 3rd parties.
      • But a House Intel Committee Member warns that DNA test kits could lead to targeted bioweapons.
      • The LA County Sheriff’s Department announced they will not work with a China-linked genetics firm hired by the county to conduct COVID testing and registration because the FBI shared “very concerning information” about Fulgent Genetics Corporation – which was awarded a no-bid contract for the work.  LASD states DNA data from COVID testing is not guaranteed to be safe and secure from foreign governments and “will likely be shared with the Republic of China.”
        • China just happens to be quietly building the worlds largest DNA database.  All those COVID tests results will come in handy.
        • The FBI is shocked to find that China’s offer to build $100 Million ‘garden’ in DC just might be for espionage purposes.
        • There is growing concern over Chinese interests purchasing large swaths of land, particularly farmland, in the U.S. – including one sensitive parcel in North Dakota in the proximity of a military installation.
        • While Americans are paying $5 per gallon of gas, DOE docs show the Biden admin has sold nearly 6 million barrels of oil from the U.S. strategic reserve to an entity tied the CCP (Sinopec, parent org of Unipec through BHR Partners), which in turn has ties to Hunter Biden. The Biden admin. has also shipped more natural gas to Europe than promised.
    • Fosun obtained the Medicines Patent Pool (MPP)’s license to produce and supply the generic versions of:
      • Merck’s oral COVID-19 treatment Molnupiravir 
      • Pfizer’s oral COVID-19 treatment Nirmatrelvir
      • Pfizer’s Nirmatrelvir and Ritonavir
    • Fosun, a CCP-owned hybrid entity is making millions off of Pfizer injections, Monupiravir, and Paxlovid, so when Biden does a deal with Pfizer with our tax dollars, and gets billions in omnibus bills for PPE, including millions for PCR and antigen tests, he is writing checks to China.
    • A 2018 whistleblower broke a scandal revealing that Fosun Pharmaceuticals had “massively” faked its data and bribed regulators. The FDA wrote them a stern letter.

Important quote:

So take all of the above, and map it against the 150,000 plus adverse events in the Pfizer documents, the deadly harms to reproduction, the Western baby die-off, the babies in seizures; map it against the population drop, the rise in disabilities, map it against the rigid, cruel vaccine mandates aimed at Western defense forces (Canada’s, and Australia’s and all of Western Europe’s, as well as at the most powerful military in the world, that of the United States) — map it against the vaccine mandates aimed at our police, our health care workers, our firefighters, our pilots, our first responders, our kids, our babies — all this done by a White House captive, via Hunter Biden’s laptop, to the CCP.

This all means, of course, that we are staring into the abyss right now.

Traumatized or not, we all need to snap out of denial.

We let our adversary come too close to us. Into our very bloodstreams.

We need to save each other.

We need to turn and face the ravening beast.

Category:

Activism, Testing, vaccines, Viruses

Public Health Vaccine & Treatment Fraud

https://popularrationalism.substack.com/p/how-fauci-and-grady-lowered-the-standards

How Fauci and Grady Degraded the Standards of Ethical Requirements for Clinical Research in the US Compared to the Rest of the World

In reading Nuremberg, The Belmont Report, and now the Helsinki Declaration, I can say that up to 2020, US had far lower ethical standards for human subjects research than WMA. Now? None.

James Lyons-Weiler
Excerpts:

Both WHO and the US HHS suffer from a form of ethical blindness when it comes to vaccine research. Foregoing long-term vaccine safety studies in favor of retrospective analysis of real-world data, these agencies fail to recognize that post-marketing (and post-EUA) studies are de facto uncontrolled, non-randomized prospective clinical trials conducted without proper consenting procedures.

If you’ve read the Nuremberg Code, the Belmont Report, and the Declaration of Helsinki, you’d know that protections are supposed to be in place not for some people undergoing some clinical studies, but instead are considered to be required to be in place for all people undergoing any clinical studies.

Where the US had departed (prior to 2020) from the rest of the countries that backed Helsinki (WMA) and participated in its updates included, according to Kimmelman et al. (2009) included:

  • Disclosure of conflict of interest
  • Public disclosure of study design
  • Benefit for populations in which research is conducted (beneficence)
  • Reporting of accurate results and publication of negative findings
  • Access to treatment after research has been conducted
  • Restriction of use of placebo in a control group where effective alternative treatment is available

The departure formally came when issues related to HIV clinical trials run in less wealthy countries seemed to depart from Helsinki standards. Rather than work to reconcile differences with Helsinki, US companies, and the US government came up with a different international standard called “Good clinical practice” – standards in place in the EU (codified as Directive 2001/20/EC), and the US (enforced as policy by NIH), all backed by Pharma.

The departure of the US and the EU from the countries that continue to abide by Helsinki serves to empower those running clinical trials at the expense of those individuals taking on the risk of new drugs and vaccines – both in the risk of poor efficacy and in the risk of potential safety issues.

Well, it turns out that Fauci was at the forefront of the war on ethical research, arguing against the requirement of the use of placebos in HIV drug trials in Africa.

Fauci’s insistence on no placebo arm in HIV drug trials in Africa is an example of bluster and posturing on morality to hide the negative consequences (harm) of the drug AZT. We’ve seen this bluster and posturing all along with COVID-19 vaccines, and Fauci’s denial of the efficacy of early treatment. He rolls over so many of the principles of medical research ethics – and ethics of care – those that were meant to be sacrosanct to protect the interests and well-being of individuals, as outlined in Nuremberg, Helsinki, and the Belmont Report.

Medical hubris has been the modus operandi of Fauci well before COVID-19.

It’s time to revisit why and how it came about that the pharmaceutical companies are able to write the rules by which they conduct clinical research.

(See link for article)

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Please see Jeremy R. Hammond’s antidote to government and mainstream media’s disinformation:

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https://childrenshealthdefense.org/defender/fda-moderna-bypass-covid-vaccine-safety-standards-documents/

FDA Colluded With Moderna to Bypass COVID Vaccine Safety Standards, Documents Reveal

According to Alexandra Latypova, an ex-pharmaceutical industry executive, documents obtained from the U.S. Department of Health and Human Services on Moderna’s COVID-19 vaccine suggest the U.S. Food and Drug Administration and Moderna colluded to bypass regulatory and scientific standards used to ensure products are safe.

fda moderna covid vaccine safety

Excerpts:

After analyzing 699 pages of studies and test results “supposedly used by the FDA to clear Moderna’s mRNA platform-based mRNA-1273, or Spikevax,” Latypova told The Defender she believes U.S. health agencies are lying to the public on behalf of vaccine manufacturers.

“It is evident that the FDA and NIH [National Institutes of Health] colluded with Moderna to subvert the regulatory and scientific standards of drug safety testing,” Latypova said.

“They accepted fraudulent test designs, substitutions of test articles, glaring omissions and whitewashing of serious signs of health damage by the product, then lied to the public on behalf of the manufacturers.”

(See link for article)

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https://childrenshealthdefense.org/defender/biden-pharma-fda-officials-covid-booster-timeline

Biden, Pharma Pressured Top FDA Officials to Approve Booster Timeline, Emails Reveal

Judicial Watch today announced it received 112 pages from the U.S. Food and Drug Administration that show top officials being pressured by “companies and for that matter the administration, who try to impose timelines [sic] that make no sense.”

Excerpts:

The records were produced to Judicial Watch in response to a February Freedom of Information Act (FOIA) lawsuit against the Department of Health & Human Services (HHS) that was filed after HHS failed to respond to a Sept. 3, 2021, FOIA request for records of communication from the former director and deputy director of the FDA’s Office of Vaccines Research and Review, Dr. Marion Gruber and Dr. Philip Krause, respectively (Judicial Watch v. U.S. Department of Health and Human Services (No. 1:22-cv-00292)).

Drs. Gruber and Krause reportedly resigned during the White House’s push to approve the COVID-19 vaccine “booster shots.”

(See link for article)

The FOIA requests and lawsuits uncover a substantial amount of info on many COVID issues including a FBI inquiry, NIAD’s money and grants to EcoHealth Alliance and Wuhan for bat coronavirus research, Fauci emails citing ties between Wuhan and EcoHealth, Gates’ involvement with the Chinese government, HHS records showing a grant application for “gain of function” research on bat RNA, viruses, and genetic manipulation of SARSr-CoV WIV1 strain, HHS records showing the Pfizer lipid nanoparticles were found in the liver, adrenal glands, spleen, and ovaries of test animals 8-48 hours after injection, safety lapses at U.S. biosafety labs, and HHS records showing NIH officials tailored confidentiality forms to China’s terms.

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HFDF ANNOUNCES LEGAL ACTIONS IN PARTNERSHIP WITH DAILYCLOUT

Leslie Manookian, HFDF President, has partnered with Dr. Naomi Wolf, DailyClout CEO, to hold the FDA accountable for its unscrupulous and unlawful approval of remdesivir for all patients, and COVID injections for young children.

Category:

Activism, Treatment, vaccines

WHO Declares Monkeypox Outbreak a Global Health Emergency After Only 5 Deaths & A Vaccine-Derived Polio Case in NY

https://www.theblaze.com/news/monkeypox-global-health-emergency-who

WHO declares monkeypox outbreak a global health emergency after 5 deaths worldwide

Paul Sacca

July 23, 2022

The World Health Organization (WHO) has declared the monkeypox outbreak a global health emergency.

“I have decided that the global monkeypox outbreak represents a public health emergency of international concern,” WHO Director-General Tedros Adhanom Ghebreyesus announced on Saturday morning during a briefing in Geneva.

Members of an expert committee met on Thursday to decide if the current monkeypox outbreak should be escalated to a public health emergency of international concern (PHEIC). Of the virologists, vaccinologists, epidemiologists, and health experts, nine voted against declaring monkeypox a PHEIC, and six voted in favor, according to Reuters.

The International Health Regulations Emergency Committee were “resolved by consensus to advise the WHO Director-General that at this stage the outbreak should be determined to not constitute a PHEIC.”

“However, the Committee unanimously acknowledged the emergency nature of the event and that controlling the further spread of outbreak requires intense response efforts,” according to the WHO. “The Committee advised that the event should be closely monitored and reviewed after a few weeks, once more information about the current unknowns becomes available, to determine if significant changes have occurred that may warrant a reconsideration of their advice.”

(See link for article)

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SUMMARY:

  • Tedros overrode the committee & gave monkeypox the highest level of alert.  So much for having experts and a committee.
  • The big takeaway is the designation gives the WHO authority to raise public awareness to raise funding and resources from member nations.  In short, this is a great moneymaker and we don’t want to miss out on that.
  • This is the 7th alert declared since 2007.  The other six were:
    • H1N1 influenza pandemic of 2009 (the fast-tracked H1N1 vaccine increased miscarriages, narcolepsy, and febrile convulsions in 1 in every 110 in Australia). The WHO by May, 2006 stated H1N1 only killed 100 people. H1N1 is another scam.
    • Ebola outbreak in West Africa from 2013 to 2015 (Please read Dr. Rowan’s successful experience with ozone in Sierra Leone.
    • Ebola outbreak in the Democratic Republic of the Congo from 2018 to 2020
    • Zika outbreak in 2016. (Please read this showing they took TWO tissue samples from TWO fetuses containing Zika to “prove” causation.  Rather than taking years to complete lab work, they took ONE paper & plopped it into Shepherd’s criteria where it only met 3 of the 7 criteria, to establish a causal link).  Zika was another scam.
    • poliovirus that started in 2014
    • COVID-19 pandemic.  A complete and utter scam.
  • Tedros admits the outbreak is concentrated in gay men, particularly those who have multiple partners.
  • There is a total of FIVE monkeypox deaths worldwide
  • Predictably, BARDA has purchased a total of 6.9 million monkeypox vaccines through mid-2023.
  • Experts are warning that using a small pox vaccine to prevent monkeypox could cause a global smallpox (vaccinia) epidemic.

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https://www.scientificamerican.com/article/new-york-polio-case-revives-questions-about-live-oral-vaccine/

New York Polio Case Revives Questions About Live Oral Vaccine

An unvaccinated person became infected with the virus, which can be traced to a live, weakened virus commonly used in the oral polio vaccine abroad
By William Petri, The Conversation US on 
New York Polio Case Revives Questions About Live Oral Vaccine
TEM of Polio viruses: the causative agent of poliomyelitis (infantile paralysis). Although rounded in shape, each virus has a cubic symmetry. They are RNA picornaviruses. RNA genetic material occurs in the core of each virus, surrounded by a protein coat (blue). Credit: Eye of Science/Science Source

Excerpt:

The New York patient reportedly contracted a form of polio that can be traced back to the live, but weakened, poliovirus used in the oral polio vaccine. This version of the vaccine has not been used in the U.S. since 2000. Health officials said the virus affecting the male patient, who has muscle weakness and paralysis, likely originated somewhere overseas, where oral vaccines are still administered.

(See link for article)

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**COMMENT**

The article misleadingly states that vaccines introduce a harmless version of a pathogen to your body to train your immune system to fight off the real germ if you ever encounter it.

This is the narrative we’ve been told ad nauseum, yet people are damaged and killed by vaccines daily.

For a great read on the biological mechanisms of vaccine injury please read part 1 and part 2.  This reality is similar to the reality of chronic Lyme/MSIDS. It just isn’t discussed, believed, or acted upon by mainstream medicine.  And similarly, according to mainstream medicine, both topics (Lyme/MSIDS & vaccines) state everything is rare, even when it isn’t.

Regarding polio, many believe routine vaccination may have replaced one disease with another and that acute flaccid myelitis (AFM) outbreaks – a polio-like disease- have been recorded on a biennial basis.

For decades, it’s been known that under certain conditions a phenomenon referred to as “provocation polio” can occur after injections, including injections of vaccines. Yet this issue is being largely, if not entirely, ignored in today’s discussions about AFM.

And while we all envision frightening posters of kids in iron lungs, the very contagious enterovirus infection usually causes mild flu-like symptoms or no symptoms at all, and most people recover from polio without lasting health problems (nonparalytic polio).

While the global poliovirus eradication effort appears to have been successful, the consequences of routine use of OPV are not fully known. In 2009, the World Health Organization warned that live polio vaccine may be responsible for a rise in vaccine strain polio termed Vaccine Derived Polio Disease (VDPD).

Not only has live vaccine strain poliovirus been found to cause paralytic disease in some cases, but evidence also shows that mutated vaccine-derived viruses are responsible for some outbreaks.15,16 As reported by NPR in 2017:

“For the first time, the number of children paralyzed by mutant strains of the polio vaccine are greater than the number of children paralyzed by polio itself. So far in 2017, there have been only six cases of ‘wild’ polio reported anywhere in the world …  Source

We are always given part of the truth – not the whole enchilada. Vaccines have always come with risks and always will.  
The polio case might be a foreshadowing of smallpox in the future.

Category:

Activism, vaccines, Viruses

FDA Relied on Scientific Fraud to Authorize Pfizer’s COVID Shot For Infants/Toddlers & Israel Caught Concealing “Vax” Injuries

https://popularrationalism.substack.com/p/hammond-fda-relied-on-scientific

Hammond: FDA Relied on Scientific Fraud to Authorize Pfizer’s COVID-19 Vaccine for Infants and Toddlers

A Guest Post by Journalist Jeremy R. Hammond

James Lyons-Weiler

I invited objective and ethical independent journalist Jeremy R. Hammond to share his latest in his series of newsletters summarizing how the FDA relied on scientific fraud to authorize Pfizer’s COVID-19 vaccine for infants and toddlers. In this piece, he reports how the FDA attempted to justify its decision by exaggerating the risk to children from “Long COVID“.

If you missed the prior newsletters in this series, you can read Part I here (introduction to the FDA’s willful dishonesty), read Part II here (willful ignorance of natural immunity the very low risk to children), and read Part III here (lying about the risk of hospitalization).

Since it is widespread common knowledge that the risk to children of dying from COVID-19 is statistically zero, and the risk of hospitalization is also extraordinarily low, the FDA in its emergency use authorization decision memorandum highlighted the risk to children of Long COVID.

The FDA acknowledged that the data are “sparse” but cited a report from the UK Office for National Statistics finding that 7.2% of children who tested positive for SARS-CoV-2 reported continued symptoms at 12 weeks post-infection.

Thus, the FDA implies that seven out of every one-hundred children infected with the virus may develop Long COVID.

However, because that report was based on a survey of self-reported symptoms and was otherwise not methodologically sound enough to estimate the true rate of long-term symptoms in children attributable to SARS-CoV-2 infection, the UK report explicitly states, “It is not possible to infer from this analysis whether self-reported symptoms are caused by coronavirus infection.”

That naturally didn’t stop the FDA from fraudulently drawing precisely that inference in order to push its emergency use authorization through.

Estimates from such surveys or observational data of the proportion of people who develop persistent symptoms after SARS‑CoV‑2 infection are confounded by other causal or contributing factors, including the negative health effects of governments’ “lockdown” measures and the traumatism of simply having tested positive resulting from the persistent and intensive fearmongering about the risks from the virus emanating incessantly from the government and mainstream media over the course of the pandemic.

An article in JAMA in October 2020 astutely observed that the negative health effects of the government lockdowns and general trauma to the population needed to be differentiated from true cases of persistent symptoms caused by SARS-CoV-2 infection.

A study in Acta Paediatrica in April 2021 found that 43% of children previously diagnosed with COVID-19 reported one or more symptoms more than 60 days post-infection, but the authors emphasized that they lacked a control group and that their finding was confounded by the negative health effects of the lockdowns, and they therefore called for further studies to be done including a control group to estimate the true prevalence of Long COVID.

A study by German researchers on the preprint server medRxiv in May 2021 did include a control group and found no statistical difference when comparing the reported persistent symptoms of adolescents who tested positive for antibodies to SARS-CoV-2 with those who tested negative.

A study by Swiss researchers reported in JAMA in July 2021 found that 4% of children who tested positive for antibodies to SARS-CoV-2 reported at least one symptom lasting more than 12 weeks, which compared to 2% of children who reported persistent symptoms but had no evidence of prior infection.

A study by UK researchers on the preprint server Research Square in August 2021 found that 67% of children and adolescents reported persistent symptoms three months after having tested positive for SARS-CoV-2, but this compared with 53% of children who tested negative. As the authors appropriately noted,

“it is unclear whether the features associated with Long COVID are related to the viral infection or the effects of the pandemic, lockdown and school closures with consequent social isolation.”

A particularly illuminating study by French researchers in JAMA Internal Medicine in November 2021 found reported persistence of symptoms to be associated with the mere belief among subjects that they had previously been infected with SARS-CoV-2. With the sole exception of loss of taste or smell, they found no significant difference in the rate of self-reported symptoms between individuals who had evidence of prior infection and those who believed they had been infected but tested negative for antibodies.

The authors appropriately concluded that “persistent physical symptoms after COVID-19 infection may be associated more with the belief in having been infected with SARS-CoV-2 than with having laboratory-confirmed COVID-19 infection.” They further cautioned that practitioners should do a careful medical evaluation so as not to erroneously attribute symptoms to “Long COVID“.

A systematic review and meta-analysis published in the Journal of Infection in November 2021 found an inverse association between the quality of studies and estimated prevalence of Long COVID in children: specifically, the higher the quality of the study, the lower the estimated prevalence.

Narrowing their analysis to only those studies that included a control group, they found that the frequency of most persistent symptoms reported by people who tested positive for SARS-CoV-2 was similar to that reported by people who tested negative. The authors appropriately concluded by emphasizing the importance of including a control group so as not to artifactually inflate the prevalence of Long COVID in the childhood population.

In sum, the FDA’s reliance on a single source from which it is logically “not possible to infer” whether the self-reported symptoms were caused by SARS‑CoV‑2 infection to willfully mislead people into the belief that more than 7 percent of children infected may develop Long COVID is just another illustration of how the agency serves the pharmaceutical industry by engaging in deliberate fearmongering and scientific fraud.

Furthermore, even if we were to assume for the sake of argument that over 7 percent of children do develop Long COVID, the FDA failed to produce any data to support its assumption that vaccination would reduce that risk.

The FDA acknowledges this failure, noting understatedly in its “limitations” section that “available data are not conclusive on the effectiveness of COVID‑19 vaccines currently in use against long-term sequelae of COVID‑19 among individuals who are infected despite vaccination. Additional evaluation is needed to assess the effect of this vaccine in preventing long-term effects of COVID‑19, including data from clinical trials and from the vaccine’s use post-authorization.”

To justify its authorization of the vaccine for infants and toddlers, the FDA simply assumed that it would be protective against persistent symptoms following breakthrough infection — once again, a faith-based and not evidence-based approach.

In my next newsletter, I’ll go over how the FDA misled about the risk of myocarditis from COVID-19 versus the risk of myocarditis from COVID-19 vaccination.

Wow. Jeremy is spot-on, and thorough. I would like to suggest that all of my readers head to JeremyRHammond.com and sign up for his free newsletter for more content like this, that would be perfect. Each of the newsletters in this series is a summary version of a section of the major paper he is working on, which he will be publishing as a downloadable e-book, so subscribers can also stay tuned for that more extensive and fully reference

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https://ahrp.org/israel-was-caught-concealing-childrens-vaccine-injuries/

Israel Was Caught Concealing Children’s Vaccine Injuries

July 19, 2022

by Vera Sharav
Alliance for Human Research Protection

Israel’s Ministry of Health commissioned a study analyzing reports of adverse events from Pfizer’s COVID vaccine to Israel’s vaccine database, known as the Nahlieli system, between December 2021 and May 2022. The research team was headed by Professor Matti Berkowitz, director of the Clinical Pharmacology and Toxicology Unit at Assaf Harofeh Hospital (Shamir).

Prof. Berkowitz’s team found that children in the 5-11-year age group had twice to four times as many adverse events following the Pfizer shot as children in the 12-17 age group. This doubling of vaccine injuries is, in itself, extremely disturbing — and should have been immediately brought to the attention of the nation’s parents.

The parents were not informed. What’s more, the Ministry officials recommended booster shots for youngsters aged 5-11—thereby increasing the risk for serious harm.

Furthermore,  the doubling of adverse events is only the beginning of the bad news.
As Dr. Yaffa Shir-Raz, a health and risk communication researcher at the University of Haifa and at Reichman University, explained: the 2-dose immunization rate for 5 to 11-year-olds is less than 18%, while older children have rates of 55-72% (3-4 times higher).

“That means that the young children would thus be expected to have ⅓-¼ of the number of adverse events experienced by the older children, not twice as many. This means that the adverse event rate for young children is actually 6-8 times that of the older children, i.e., at 600-800% of the baseline injury rate!”

It is unconscionable that the Israeli Health Ministry knew about the serious risks of harm posed to young children, concealed the evidence, and further expanded the ever-increasing risk for children by authorizing the use of these UNSAFE and medically unjustifiable genetically manipulated injections for infants and toddlers!

(See link for article)

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To gain insight into the scope and magnitude of harm to individual, previously healthy Israelis, I highly recommend that you check Avital Livni’s Israel Testimonies Project

The Testimonies Project was created to provide a platform for all those who were affected after getting the covid-19 vaccines, and to make sure their voices are heard, since they are not heard in the Israeli media.

We hope this project will encourage more and more people to tell their story.

For more:

Category:

Activism, vaccines, Viruses

Neurologist Weighs in on Spate of SADS: “We Should Be Doing Autopsies on Every Single One”

https://jennifermargulis.substack.com/p/we-should-be-doing-autopsies-on-every

“We Should be Doing Autopsies on Every Single One”

A neurologist weighs in on the spate of sudden adult deaths

Jennifer Margulis

Robert Lowry, M.D., is a concussion and musculoskeletal expert who has been practicing medicine for over 25 years. When I spoke with him by phone last week, Lowry told me he’s seen an upsurge in young patients—adults under 40—coming to him with neurological problems.

These problems, he said, include everything from severe headaches to Bell’s palsy (facial paralysis) to strokes.

In every case he has seen, Lowry said, his patient was vaccinated. For this reason, he believes these neurological issues are actually COVID-19 vaccine adverse events.

Data From Mexico

Lowry pointed me to a 2021 article in Clinical Immunology that analyzed vaccine injury data from Mexico.

The study authors found that about 1 percent of people who got the first dose of the Pfizer vaccine reported having adverse neurological events afterwards.

Less than one percent. No problem. Right?

But, Lowry argued, that number is likely underreported by a factor of 10. And, he insisted, even if it is accurate, that percentage of adverse neurological events is simply too high to justify vaccination in otherwise healthy young adults.

(See link for article)

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SUMMARY:

  • If 2/3 of the population got one dose, that is 5.3 billion people.  1% of 5.3 billion equals 53 MILLION who have likely already suffered from neurological injury.
  • You can calculate your risk of dying from COVID-19 by entering your age, place of residence, and underlying health issues into an online risk calculator.
  • Since the risk of dying from COVID for young adults is less than 1%, risk of injection damage outweighs any supposed benefit.
  • Healthy people are suddenly dying (SADS) in numbers never seen before.
  • When the deaths are “unexplained” but a history of vaccination within the past 12 months, Dr. Lowry believes the cause is likely the mRNA vaccines.
  • Physicians are seeing many more severe reactions and neurological and cardiac injuries after the second dose.
  • The most likely ways include micro-clots in the brain that result in neuron necrosis; myocarditis, pericarditis and other heart damage; and vasculitis (inflammation of the blood vessels), but is compounded by immuno-sensitivity.
  • The best way to find out the cause of these cases is by doing autopsies, and Lowry believes autopsies should be done on every single one of these healthy people who died suddenly.

Please note that Fauci told the government to tell others to NOT do autopsies on COVID patients.  Doctors are asking where the autopsies are of those who died after the COVID shots. Embalmers are showing blood clots and white, fibrous structures in the “vaxxed,” and that hospitals are covering up the deaths of babies by cremating them in house.

Autopsies would also give answers in Lyme-land.

Category:

Activism, vaccines, Viruses