#PFIZERLEAK - THE ISRAELI CONNECTION
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Was Dr. Robert Malone wrong about his claims about the contract between Israel and Pfizer? Does the Israeli government has an agreement not to disclose adverse events for a minimum of 10 years?
Time to set the records straight.
I don't like bullies. It is one thing for someone gets upset and call you an idiot. It is completely different when a whole smear campaign is being conducted against an individual because of their believes, which is what @TheAtlantic did to @RWMaloneMD
Since I was the person who was interviewed by The American Frontline Doctors which is the tweet he quoted, I thought it is time to address this disgrace of an "article". This is the hit piece of that appeared in The Atlantic, written by Tom Bartlett. theatlantic.com/science/archiv…
1) does @TheAtlantic claims @RWMaloneMD claims about Israel are misleading speculation or plainly false? Please be clear. 2) "hard to believe" is not investigative journalism, it's an opinion. Did Tom look at the facts and see what exactly is going on between Israel and Pfizer?
First, let us look at the specific case mentioned by The Atlantic.
Tom claimed that "the country’s health ministry has already warned of a link between the Pfizer shot
and rare cases of myocarditis."
Let us first look at the press release: 1) Even though myocarditis usually appears among younger men, aged 16 to 30, the report admits it started to appear among the younger age group, 16 to 19.
2) 275 cases were mentioned, 148 around the shot.
3) The PR mentioning the total # of individuals who got the shot is statistical fallacy. Since the majority of those who got myocarditis were from the age group of 16 to 19, there should have been focus on the # of vaccinated among that group as it is the major risk group.
4) 95% were considered to be mild cases - is it for the whole 275 cases mentioned, or for the 148?
5) Does the press release means 7 young people at the age of 16 to 19 got severe myocarditis (95% of 148) or 14 out of the total population, and if so what age where they?
Let's dig deeper.
Here is the link to the epidemiological team, who published "Short Communication" called "Myocarditis following COVID-19 mRNA vaccination"
First, a reminder to the Ministry of health press release:
"In most cases myocarditis took the form of mild illness that passed within a few days."
And here is the epidemiological team statement:
"myocarditis may have a more severe clinical presentation, may impose limitations on physical activity and may require long-term medical treatment, and follow-up"
Can you spot the difference ?????????
Next, the majority of the cases, as the MoH, were of young people at the age of 16 to 19, yet only two cases out of 6 which were reported about were at that group.
The selection criteria for this research is not in line with the distribution among population.
Next,
The hospital serve 500K, average 1.17 cases per month. 6 patients presented in less than a month.
Israel allowed 16yrs to 18yrs get the shot at the end of January.
1) How many of the 500K got the shot? 2) How many between the age 16 to 18? 3) Are the 6 the only cases?
As you saw, the report of the Ministry of Health, the way it is structured and it's conclusions, alongside the very small selection group and the inability to extract meaningful information from it with regards to the real risk is weird... until you read the Pfizer contract.
The research contract between Pfizer and Israel is called "REAL-WORLD EPIDEMIOLOGICAL EVIDENCE COLLABORATION AGREEMENT" and you can find it here:
The "product" are all vaccines (see #PfizerLeak for definition) for the PREVENTION of the human disease COVID-19 OR ANY OTHER DISEASE caused by SARS-CoV-2 strains, mutation, MODIFICATIONS or derivatives.
1) The product does not prevent the disease. 2) What modifications?
Project: epidemiological data analyses, as described
in Section 2 and Exhibit A.
Sec 2: measure and analyze epidemiological data arising from the Product.
Ex. A:
Additional subgroup analyses and vaxines effectiveness analyses, AS AGREED BY THE PARTIES.
As you can see by the agreement above, THE PARTIES must agree to perform a test.
The Israeli MoH cannot decide to do "subgroup analysis" by itself. PFIZER NEED TO AGREE ON IT.
The contract seems to be indefinite, until completion of the Project (IF EVER).
Publications:
"PFIZER and MoH will jointly prepare and publish the Results in submissions) for publication, to peer-reviewed scientific or medical journals."
The Israeli MoH is "allowed" to communicate to the public anything OTHER THAN what they "measure and analyze (in the) epidemiological data arising from the Product rollout"
I guess the Israeli MoH can still publish the weather, right?
If one side want to publish epidemiological data arising from the Product rollout ON THEIR OWN (e.g. MoH), the other side must be given this in advance for it to provide comments.
Confidentiality:
Pfizer has the right to ask for "the deletion of any reference to the other Party’s Confidential Information from the proposed disclosure or publication".
Confidential: Technology, research, Pfizer Data, project data or results unless public health data.
"All disclosures and publications must expressly acknowledge the other Party, unless such Party objects to such acknowledgment"
THERE IS MORE BELOW!!!
Press the "Show replies"
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If Pfizer & MoH does not agree on publication of information, it will need to be agreed between (someone) in Pfizer and Sharon Alroy-Preis, who works for the MoH as Israel's director of public health services.
Sharon Alroy-Preis was a co-author of "Impact and effectiveness of mRNA BNT162b2 vaccine against SARS-CoV-2 infections and COVID-19 cases, hospitalisations, and deaths following a nationwide vaccination campaign in Israel: an observational study using national surveillance data"
So Sharon Alroy-Preis, the person who is suppose to negotiate in case Israel wants to publish something has been a co-author of a publication which was using the project data.
Sharon Alroy-Preis works for the MoH, who signed the manufacturing the supply agreement with Pfizer and agreed to indemnify, defend and hold harmless Pfizer...against any and all suits, claims...caused by, arising out of, relating to, or resulting from the Vaccine" #PfizerLeak
So, what did we learned so far? 1) @TheAtlantic "journalist" didn't do any journalism but a hit piece, without looking at the evidence.
2) Isreal's MoH reporting seems to be extremely biased towards downgrading adverse events, trying to bury them.
3) The contract itself has no expiration date, which gives incentives to both parties to make it last as long as possible. For Israel MoH, it means people who work in the project has a job, get published in magazines (e.g. Sharon Alroy-Preis), and have no incentives to stop it.
4) There is no clear definition what is "public health data" in the contract; epidemiological data is considered to be project data, not public health data. Pfizer and MoH need to agree on new epidemiological investigations.
5) There are conflicts of interest both on MoH, who is suppose to protect Pfizer from any legal claims and yet it runs this project, and on a personal level, by assigning an individual who works for the MoH as a mediator, who also is directly involve in the project.
6) I think that what I found is much worse than the claim of the scientist who told @RWMaloneMD that the Israel and Pfizer will not disclose adverse events for a minimum of 10 years. The research contract is heavily redacted & the Manufacturing & supply contract was not exposed.
7) I INVITE YOU TO READ THE EVIDENCE AND DECIDE FOR YOURSELF.
Finally, @RWMaloneMD - thank you for your courage for speaking out and withstanding the waves of slur. What an inspiration.
As was brought to my attention, this smear job was supported by grants from Chan Zuckerberg Initiative and the Robert Johnson Foundation, a member of the World Economic Forum (WEF).
"It's a big club, and you ain't in it!" (George Carlin).
#PFIZERLEAK - THE ISRAELI CONNECTION - APPENDIX A.
BLOG POST ABOUT THE BRAZILIAN CONTRACT:
✓ STEP-BY-STEP VALIDATION OF THE CONTRACT
✓ ANALYSIS OF CONTRACT CLAUSES
✓ STATEMENT BY SENIOR PFIZER EXECUTIVE ALL COUNTRIES SIGNED SUCH CONTRACT #PfizerLeak
Pediatric Moratorium! Adult Use Restrictions! Veterinary Prohibition!
"Codon Optimization in mRNA Vaccines and Gene Therapies: An Assessment of Protein Misfolding Risks and Regulatory Oversight" submitted to the FDA's Vaccines and Related Biological Products Advisory Committee!
Here's the Executive Summary
Objective: This white paper evaluates the scientific evidence and regulatory oversight related to codon optimization in messenger RNA (mRNA) vaccines and gene therapies for both human and animal applications. Its primary goal is to assess whether the potential risks—specifically protein misfolding, aggregation, and associated diseases like amyloidogenesis and prionogenesis—justify a moratorium on this technology’s use. The analysis aims to inform policy by balancing innovation with safety.
Scope: The assessment covers the principles of codon optimization, the mechanisms of protein folding and misfolding during translation, and the risks of amyloid formation and prion-like propagation. It reviews regulatory frameworks, including the U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA) Chemistry, Manufacturing, and Controls (CMC) requirements. The scope includes a detailed examination of scientific literature—both foundational and recent—such as studies on tissue-specific codon usage, codon context effects, and structural risks in mRNA vaccines. It also analyzes preclinical and clinical safety data, pharmacovigilance reports, and a case study on COVID-19 mRNA vaccines. Additionally, the paper explores implications for veterinary vaccines and food chain safety, concluding with an updated risk management and policy evaluation.
Key Findings: Codon optimization enhances protein production in mRNA-based vaccines and therapies but introduces risks that challenge its presumed safety. New research shows that changing codons—previously thought to be neutral—affects translation speed and accuracy, potentially leading to protein misfolding and aggregation. For example, the cardiomyocyte PAO model reveals that misfolded proteins can cause delayed, severe damage, such as heart failure, broadening concerns beyond brain-related diseases. Data from TissueCoCoPUTs indicate that generic codon optimization often mismatches the translation needs of specific tissues, increasing misfolding risks. In COVID-19 mRNA vaccines, structural issues like excessive G-quadruplex formation may heighten these dangers.
Regulatory oversight, however, falls short. There are no standard tests to evaluate how codon changes affect protein shape or clumping, and long-term monitoring is insufficient to detect slow-developing issues like neurodegeneration or prion-like diseases. The rapid rollout of COVID-19 mRNA vaccines lacked thorough evaluation of these folding risks. In veterinary applications, the use of codon-optimized therapies in livestock raises unresolved concerns about misfolded proteins entering the food chain and environment, potentially affecting human health.
Conclusion on Moratorium
Given the mounting evidence of risk and gaps in oversight, a tiered moratorium is recommended as the most cautious and effective approach:
· Pediatric Moratorium: Codon-optimized mRNA vaccines and gene therapies should not be used in children under 18 until safer practices are developed. This includes using tissue-specific codon designs, conducting 24-month safety studies in primates, and setting limits on G-quadruplex formation. Children’s developing tissues are especially vulnerable, and long-term data are lacking.
· Adult Use Restrictions: New clinical trials for risky mRNA designs—those with heavy optimization, high clumping potential, or rich GC content—should pause. This halt would last until advanced tests, such as Kinetic Folding Assurance (KFA), hidden gene screening, and cross-seeding checks, are required.
· Veterinary Prohibition: Codon-optimized gene therapies in animals entering the food supply should be banned. Evidence from the PAO model and prion diseases suggests a risk of transmissible misfolded proteins, posing a threat to food safety.
This moratorium should persist until:
· Reliable tests for protein folding and clumping are part of regulatory standards.
· Codon optimization accounts for tissue-specific needs and translation timing.
· Independent research verifies the safety of high-risk designs and pediatric use.
· Better monitoring systems track long-term health effects.
This approach marks a shift in how codon optimization is viewed: it’s not just a tool for efficiency but a process that demands careful study of its effects on protein structure and safety over time. By adopting these measures, we can protect public health while still advancing mRNA and gene therapy innovations.
The whitepaper has just been published in my Sub/I\Stack (Link in my pro/I\file)!
I published my first article on codon optimization risks and the COVID-19 vaccine in August 2021 (#COptiGate) and wrote extensively on the topic. This white paper, submitted to the @US_FDA, is my final attempt to highlight our regulators' complete failure.
🚨Microwave Ovens Might Be Risking Your Health! 🚨
Did you know that eating microwaved food could cause blood changes linked to cancer? Russians knew it. Swiss scientist Dr. Hans-Urich Hertel discovered this over 30 years ago, but the microwave industry tried to silence him.
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Dr. Hans-Urich Hertel was a Swiss food scientist who challenged microwave safety. In 1989, he teamed up with Professor Bernard Blanc to study how microwaved food affects us. Their findings? Alarming enough to spark a decade-long battle! #ScienceHeroes #MicrowaveResearch
Hertel and Blanc recruited eight volunteers from a macrobiotic institute in Switzerland. For eight weeks, they ate raw, conventionally cooked, or microwaved foods—like milk and veggies—under strict conditions (no smoking, alcohol, or sex!). Blood tests followed every meal. #MicrowaveStudy #HealthResearch
Iran’s leaders aren’t just building nuclear weapons for power—they’re building them to trigger the end of the world. This isn’t geopolitics. It’s prophecy, and we’re all targets. Buckle up for a thread that’ll shake you awake.
🧵 1/20
Shia Islam has a figure called the Mahdi—a messiah who’ll return to bring justice and peace. Beautiful, right? Except Iran’s ruling clerics don’t just wait for him. They believe it’s their job to force his arrival. And they’re deadly serious.
🧵2/20
To these fanatics, the Mahdi’s return is a divine mandate they’re tasked to fulfill. They see Iran as the chosen instrument to prepare the world for him. Patience isn’t their virtue—action is. And that action could be catastrophic.
🧵3/20
THE GLOBAL IT OUTAGE YOU WITNESSED WAS NOT AN ACCIDENT!
IMPORTANT! The purpose of this thread is to explain non-IT and to non information/cyber security professionals why I believe the outage you are seeing around the world due to the update from #Crowdstrike is not an accident.
Before we begin - introduction.
Hi everyone. My name is Ehden Biber. I'm known as the person behind #PfizerLeak, and most of my writing here on X/Twitter has been on ph@rma related topics. HOWEVER, my professional work has been information security and cybersecurity.
My credentials include:
· Head of information security in Metro Bank (UK).
· Merck/MSD Information security office for Europe, Middle East and Africa (EMEA).
· Consultant to insurance and financial institutes.
The opinion you are about to read is based on YEARS of experience.
"MEDICAL GENETICS…WILL BE THE SOUL OF PERCISION MEDICINE IN EVERY FIELD"
It is time to expose another member of the W.H.O. science council and her views on genomics and gene therapy (mRNA). Introducing Dr Mary-Claire King.
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Doctor Mary-Claire King is a very known geneticist who has discovered in 1990 BRCA1,which was the first gene for a hereditary form of breast cancer. She is a professor of genome sciences in the university of Washington, Seattle, USA. medgen.uw.edu/people/mary-cl…
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Her later work was focused on the genetics of schizophrenia, she is recognized as a pioneer in the development of DNA sequencing for human rights investigations, and she is also a Senior Associate Core Member of the New York Genome Center.
THE COUNCIL: INTRODUCING THE W.H.O. SCIENCE COUNCIL THAT IS ABOUT TO CONTROL YOUR LIFE.
As we approach the final stages of the #WHO coup d'état attempt, it is time to expose the group of unelected people who will control your future and their alarming agenda!
#TheCouncil
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2/ In December 2023 the WHO produced a report that sets the stage to radical changes that soon will be enforced all the citizens of the world: make gene therapy (mRNA) key technology in the fight against infectious diseases, cancer, and combat any resistance to such technologies.
3/ It called to develop new gene therapy treatments against pathogens, promote investment in "equitable" development of the technology, use it as THE medical countermeasure mechanism to tackle pandemic threats, and to combat any resistance to the technology ("misinformation").