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Did US Supreme Court Cancel Universal Vaccination?

Did US Supreme Court Just Cancel Universal Vaccination?!

Did the US Supreme Court just cancel universal vaccination because the COVID-19 vaccines are unsafe?!

Find out what’s going on, and what the FACTS really are!


Claim : US Supreme Court Just Canceled Universal Vaccination!

Alternative health / news websites are YET AGAIN claiming that the Supreme Court just cancelled universal vaccination in the United States!

Allegedly, Senator Robert F. Kennedy Jr. and a group of scientists filed a lawsuit against Bill Gates, Dr. Fauci and Big Pharma, and they won!

It is a long essay, please SKIP to the next section for the FACTS!

URGENT: Supreme Court Has Canceled Universal Vaccination In The United States

Just Got this:

Has not been in the news anywhere. Looks like we are getting closer to the Final Scene in the movie.

Please ALERT everyone in the family, friends and relatives! BREAKING NEWS !

Supreme Court has canceled universal vaccination In the United States, the Supreme Court has canceled universal vaccination.

Bill Gates, US Chief Infectious Disease Specialist Fauci, and Big Pharma have lost a lawsuit in the US Supreme Court, failing to prove that all of their vaccines over the past 32 years have been safe for the health of citizens!


Truth : US Supreme Court Did Not Cancel Universal Vaccination!

It’s 2022, and yet again, the US Supreme Court just “cancelled” universal vaccination for the 4th or 5th time?

Just like COVID-19 variants, alternative health / news websites keep regurgitating this fake story for page views.

Let me repeat this yet again – this is FAKE NEWS!

Let’s break down the individual claims, and tell you what the FACTS really are :

Claim : Supreme Court canceled universal vaccination in the United States
Verdict : False

This claim is completely false, because the United States never mandated universal vaccination in the first place!

There is, therefore, no universal vaccination for the Supreme Court to overturn or cancel.

The government continues to have broad authority to make a vaccine mandatory during a public health crisis, as decided by the Supreme Court in their 1905 decision in Jacobson v. Massachusetts.

In 1922, the Supreme Court “settled that it is within the police power of a state to provide for compulsory vaccination” in their unanimous Zucht v. King decision.

However, compulsory or mandatory vaccination is quite different from universal vaccination.

Read more : Did Joe Biden Fire Over 200 Marines For Not Taking Vaccine?

Claim : Bill Gates, Dr. Fauci + Big Pharma Lost A Supreme Court Case
Verdict : False

Bill Gates, Dr. Fauci and Big Pharma were never part of any US Supreme Court case.

The new, ultra-conservative US Supreme Court did deal public health advocates a blow in 2020, when they ruled against the State of New York in Roman Catholic Diocese Of Brooklyn, New York v. Andrew M. Cuomo.

But that Supreme Court case had nothing to do with pharmaceutical companies, Bill Gates or even Dr. Fauci.

In that case, the Supreme Court ruled that the State of New York cannot bar people from gathering in churches and synagogues during the COVID-19 pandemic.

It was a ruling against New York’s lockdown measures, not vaccines.

I should also point out that all nine justices on the US Supreme Court were fully vaccinated by 5 May 2021, as confirmed by Supreme Court spokeswoman Kathleen Arberg.

Bill Gates, NIH Director Dr. Francis Collins and NIAID Director Dr. Anthony Fauci, May 2016, Photo Credit : Bill Branson

Claim : Robert F. Kennedy Jr. Is A Senator
Verdict : False

Robert F. Kennedy Jr. is not, and has never been, a US Senator.

The writer probably confused him with his illustrious father, Senator Robert F. Kennedy, who was assassinated in 1968.

Claim : Robert F. Kennedy Jr. Filed Supreme Court Lawsuit 
Verdict : False

Robert F. Kennedy Jr. never filed any lawsuit that was brought before the US Supreme Court.

In July 2019, he filed a lawsuit against the state of New York, to overturn a new state law that bars parents from refusing to vaccinate their children on religious grounds.

His family actually spoke out AGAINST him, calling him “an outlier in the Kennedy family“, and pointing out that his uncle President John F. Kennedy and his father, Robert F. Kennedy, both promoted vaccinations to stamp out preventable diseases.

He lost that lawsuit on 9 December 2019, after the New York state law was ruled constitutional.

That lawsuit was over the measles outbreak, and happened before the world first became aware of COVID-19 on 31 December 2019.

So it had NOTHING to do with COVID-19 or COVID-19 vaccines.

Claim : mRNA Vaccine Changes Our Genetic Material
Verdict : False

It is physically impossible for vaccine mRNA to penetrate the cell nucleus, so it cannot possibly change the cell’s DNA.

The mRNA can only enter the cell cytoplasm, where it is taken up by the ribosomes to create the spike protein.

Vaccines based on the viral vector technology are the ones that enter the cell nucleus, but even that only affects a small number of cells, and does not become part of our DNA.

Vaccines do NOT integrate with our DNA. Vaccines will NOT turn us into GMOs (Genetically Modified Organisms).

Claim : mRNA Vaccine Causes Irreversible Genetic Changes
Verdict : False

The mRNA instructions in an mRNA vaccine are automatically destroyed by the cell after use. Therefore, they can only exist for a short period of time.

As these mRNA instructions do NOT enter the cell nucleus or combine with our DNA, they cannot possibly cause “irreversible genetic changes”.

Claim : Genetic Engineering Is A Crime
Verdict : False

Genetic engineering is not a crime in any country. However, countries may set limits on what is permissible.

For example, the United States allows the genetic modification of human embryos for research purposes, but forbids its implantation without FDA’s approval.

Genetic engineering is being used to develop cures for diseases like :

  • acute and chronic lymphocytic leukaemia
  • multiple myeloma
  • various muscular dystrophies
  • cystic fibrosis
  • cancers

There have already been a few approved gene therapies :

  • 2003 : Gendicine was approved in China for certain cancers
  • 2011 : Neovasculgen was approved in Russian for peripheral artery disease
  • 2012 : Glybera was approved in the US and the US for lipoprotein lipase deficiency

Claim : mRNA Vaccine Is Not A Vaccine
Verdict : False

A vaccine is simply any biological preparation that gives your body an active, acquired immunity to a particular infectious disease.

The mRNA vaccine is a vaccine, even though it does not use the dead or attenuated (weakened) virus to provide the protection.

It works quite similarly to a viral vector vaccine, in that they both use our cells to create the SARS-CoV-2 spike protein to trigger our body’s immune system.

Think of mRNA vaccines as instructions for your cells to make “enemy soldier puppets” for your immune system to train against.

Read more : Pfizer + Moderna mRNA Vaccines : How Do They Work?

Claim : COVID-19 Vaccines Cause Genetic Defects
Verdict : False

This is complete nonsense. COVID-19 vaccines do not cause genetic defects. Genetic defects are inherited, and cannot be introduced through a vaccine.

Genetic defects are also not caused by the inability to excrete toxins, which our liver and kidneys do every single day!

Vaccines also do not prevent the human body from excreting toxins. If that actually happened, vaccinated people would die within days… which obviously, did not happen.

Claim : Vaccinated People Will Die
Verdict : False

The claim by Michael Yeadon that 0.8% of people will die within 2 weeks of the first vaccination, and the rest will die within 2 years, is absolute nonsense.

Billions of people globally have been vaccinated against COVID-19, and there is no evidence of millions of people dying from the vaccines within two weeks of their first vaccination.

Frankly, if that’s true – they wouldn’t be alive to receive their second and third vaccinations, as billions of people have done.

Now that you know that this is yet another example of anti-vaccination FAKE NEWS, please SHARE this fact check with your family and friends.

Help stop the pandemic, by vaccinating against COVID-19!


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Dr. Adrian Wong has been writing about tech and science since 1997, even publishing a book with Prentice Hall called Breaking Through The BIOS Barrier (ISBN 978-0131455368) while in medical school.

He continues to devote countless hours every day writing about tech, medicine and science, in his pursuit of facts in a post-truth world.


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Did FDA Ask For 75 Years To Release Pfizer Vaccine Data?

Did the US FDA ask for 75 years to fully release the Pfizer COVID-19 vaccine data to the public?

Find out what’s going on, and what the facts really are!


Claim : FDA Asks For 75 Years To Release Pfizer COVID-19 Vaccine Data!

According to Aaron Siri, a lawyer working on the case, the US FDA just asked a federal judge for 75 years to produce the Pfizer vaccine data and documents.

A prior post explained that the FDA has asked a federal judge to make the public wait until the year 2076 to disclose all of the data and information it relied upon to license Pfizer’s COVID-19 vaccine.  Literally, a 55-year delay.

My firm, on behalf of PHMPT, asked that this information be disclosed in 108 days – the same amount of time it took for the FDA to review and license Pfizer’s vaccine.

The Court ordered the parties to submit briefs in support of their respective positions by December 6, 2021.  The FDA’s brief, incredibly, doubles down.

It now effectively asks to have until at least 2096 to produce the Pfizer documents.  Not a typo.  A total of at least 75 years.


Truth : FDA Did NOT Ask For 75 Years To Release Pfizer Vaccine Data!

This is really just some “creative hyperbole” by Aaron Siri, the lawyer working on this FOIA (Freedom of Information Act) request.

And here are the reasons why…

Fact #1 : FDA Did Not Ask For 75 Years To Release Pfizer COVID-19 Vaccine Data

First, let me be clear – the US FDA did not ask US District Judge Mark Pittman for 75 years to release the Pfizer COVID-19 vaccine data.

That is merely the “interpretation” of Aaron Siri, the lawyer working for PHMPT (Public Health and Medical Professionals for Transparency) – the group requesting the data that the FDA used to licence the Pfizer COVID-19 vaccine.

As you will see below, it’s based on ignoring facts and basic math…

Fact #2 : FDA Has To Redact Files Before They Are Released

It is not simply a matter of handing over the documents to PHMPT.

The FDA has to go through every document and redact information that are exempt from disclosure under FOIA, before it can release them.

That process is not only time-consuming, it is resource-intensive because it requires government information specialists to review each page line-by-line.

The FDA estimates that it takes 8 minutes per page to read and review records for FOIA production.

Fact #3 : FDA Has 400 Other Pending FOIA Requests

The FOIA request by PHMPT is being handled by the Access Litigation and Freedom of Information Branch at the FDA’s Center for Biologics Evaluation and Research (CBER).

This is a small department with just ten employees, including the director and two trainees. So they really have just seven people who are trained well enough to process FOIA requests.

This small team is currently processing “approximately 400 currently pending FOIA requests“, while being embroiled in “6 active FOIA litigation matters“.

Needless to say, the heavy workload greatly limits how many pages this office can go through and redact every month.

Fact #4 : PHMPT Demanded “Everything” In 108 Days

The FDA asked PHMPT to narrow their request by specifying records they don’t require, so they can focus on processing the important documents they need.

The PHMPT, however, insisted that the FDA process and deliver ALL documents related to the approval of the Pfizer COVID-19 vaccine – some 329,000 pages!

On top of that, the PHMPT demanded that the FDA accomplish that within 108 days. That would require a processing rate of over 80,000 pages per month – far in excess of what the FDA FOIA office is capable of handling.

Fact #5 : FDA Vaccine Approval Is Different From FOIA Process

It seems obvious, but it has to be said – the FDA vaccine approval process is different from the FOIA process.

So it is ridiculous for the PHMPT to insist that their 108-day demand is valid because it “is the same amount of time” it took the FDA to review the documents and licence the Pfizer COVID-19 vaccine.

The vaccine approval process involves FDA scientists evaluating the Pfizer COVID-19 vaccine for the EUA (Emergency Use Authorisation) or full FDA approval.

The FOIA process, on the other hand, involves FDA information specialists going through each page line-by-line to identify and redact proprietary information.

Fact #6 : FDA Vaccine Approval Process Adds A Ton Of New Documents

The FDA vaccine approval team went through fewer documents, because they only need to look at relevant information provided by Pfizer and BioNTech.

The FDA team in charge of this FOIA request would necessarily have to go through far more documents, because the approval process itself adds a ton of new documentation.

Even the PHMPT acknowledged that, specifically asking for “all correspondence and written summaries of oral discussions” related to the FDA approval of the Pfizer COVID-19 vaccine.

Hence, it is ludicrous for the PHMPT to claim that the two processes are similar in effort and time.

Read more : Full FDA Approval vs EUA for Vaccines : What’s Different?

Fact #7 : FDA Processes FOIA Requests In 500-Page Blocks

The FDA processes FOIA requests in 500-page blocks, which allow them to provide documents to more requesters, and avoid a few large requests monopolising their “finite processing resources”.

This is not a special processing limitation on the Pfizer COVID-19 vaccine data, but a standard FDA processing rate that the courts have upheld for a long time.

Fact #8 : FDA Processing FOIA Requests Faster Than Proposed

The FDA was able to process some records faster than the 500-page rate, as they noted in their 6 December 2021 brief. They also said that they can release more than 12,000 pages by end of January 2022.

As it stands, the FDA appears to be doing above and beyond what it pledged to do, delivering almost 5000 pages per month – about 10X its promised rate.

Even if they end up delivering half that performance, they would finish processing 329,000 pages in 137 months – just under 11.5 years.

Obviously, 11.5 years is far less than the 55 years claimed…

Fact #9 : It Would Take PHMPT Months To Read Everything

PHMPT stated that they are a group of over 30 people. Let’s say there are 35 strong, and they take the same 8 minutes to read through each page.

Even if they all sat down and read for 8 hours a day, it would take them over 7 months just to read through the 329,000 pages ONCE.

And it should be noted that this involves 5X more people than the FDA FOIA team, and they are all dedicated to this singular task of reading those Pfizer documents.

Fact #10 : FDA Will Release Almost All Of PHMPT Priority List By Jan 2022

PHMPT appears to be cognisant that it is stupid to request for “everything” when most of the pages may not be relevant at all.

That’s why they sent the FDA a priority list of eight (8) items. And guess what – the US FDA said that they will be able to furnish seven (7) of those items by January 31, 2022!

So Aaron Siri’s public griping about the FDA taking so long appears to be nothing more than theatre.

Fact #11 : Processing Time Depends On PHMPT, Not FDA

Aaron Siri claimed that the FDA disclosed in their 6 December 2021 brief that there are many more pages to process, thereby increasing the time to fully-release everything from 55 years to 75 years.

In addition to the original 329,000+ pages, the FDA discloses there is another “approximately 39,000 pages,” an additional “tens of thousands of additional pages,” and an additional 126 data files, many of which have over ten thousand rows for which the FDA intends to treat twenty rows as one page.  Assuming an average of only ten thousand rows per data file, and that its amorphous “tens of thousands of additional pages” amounts to 20,000 pages, the grand total is at least 451,000 pages.

That’s nonsense, because the processing time ultimately depends on what the PHMPT is demanding.

As the FDA noted, their initial assessment of 329,000 pages was based on their interpretation of PHMPT’s request for all information from the original Pfizer vaccine BLA (biologics licence application).

But if the PHMPT insist that they want OTHER RECORDS like BLA supplements, amendments and product correspondence, then the FDA would have to process an additional 39,000 pages.

And if the PHMPT insist that they also want the “investigational new drug applications” (whatever for?), then that’s tens of thousands of additional pages.

So the ball is really in the PHMPT’s court. They can drag this out to 100 years and more. All they have to do is insist that they want the FDA to process even more (irrelevant) pages.


Please Support My Work!

Support my work through a bank transfer /  PayPal / credit card!

Name : Adrian Wong
Bank Transfer : CIMB 7064555917 (Swift Code : CIBBMYKL)
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Dr. Adrian Wong has been writing about tech and science since 1997, even publishing a book with Prentice Hall called Breaking Through The BIOS Barrier (ISBN 978-0131455368) while in medical school.

He continues to devote countless hours every day writing about tech, medicine and science, in his pursuit of facts in a post-truth world.


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Papparich Group Ordered To Close By High Court!

This is the end for Papparich in Malaysia – it has been ordered by the High Court of Malaya to wind up its business!


Papparich Group Ordered To Close By High Court!

Last year, shareholder Chen Khairy Voon and the investment holdings company Agathisfour filed separate Winding-Up Petitions against Papparich Group Sdn Bhd on 15 May 2020 and 22 May 2020 respectively, over alleged unpaid debts of RM37.22 million

Just over a year later, the High Court of Malaya in Shah Alam ordered Papparich Group Sdn Bhd (PGSB) to wind up its business on 5 May 2021.

Chan Siew Mei of KPMG Deal Advisory Sdn Bhd was appointed as the liquidator, as per The Business Times.

According to the public notice, the Winding-Up Petition was directed to be heard before the High Court of Malaya at 9 AM on 11 August 2021.

The public notice also called for any party looking to support or oppose the Petition for the Winding-Up of Papparich Malaysia to appear for the hearing.


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