Donald Trump's tenure as the 45th president of the United States began with his inauguration on January 20, 2017, and ended on January 20, 2021.

Final update and revision of the posts I previously made, deleted, corrected to this my final version. Sorry about the corrections, these things take time to get right, given the complexity of them -

Donald Trump's tenure as the 45th president of the United States began with his inauguration on January 20, 2017, and ended on January 20, 2021. Wikipedia - note "2017-2021"

The Defense Production Act has played a role in the U.S. government’s response to COVID-19 (from about November 1st 2019 US virus release date ) pandemic.

President Trump declared a national emergency in March 2020, making the pandemic eligible for government action under the Defense Production Act.

President Trump said he invoked the Defense Production Act more than 100 times to facilitate Operation Warp Speed.

Trump has made the vaccinated all part of a "US Army experiment" and when you re-elect him, he will finish the job on behalf of his masters, whoever they are, but let us presuppose they are those I have identified in the final paragraph and others.

The vaccinated are countermeasure prototypes, for the US Army, to see the objective of a Covid-19 (vaccines) countermeasure, in the impairment of the operational effectiveness of enemy activity" by spike protein,the most antigenic and toxic part of a coronavirus" (vaccine) based on the measurable effects of their (the vaccines) deployment", by the US military's own definitions of terms used in Operation Warp Speed contracts, the (vaccine) products it commissioned "amount to bioweapons" and the vaccinated are part of the US Army experiment to see the effectiveness of their Covid-19 vaccines weapon, as explained below:

The injection of these "countermeasure prototype vaccines" which satisfy the US military definition of a biological agent into people has killed some recipients and permanently disabled increasingly large numbers of others, "resulting in their (vaccines) operational effectiveness based on the measurable effects of their (vaccines) deployment", by the US military's own definitions of (vaccines) terms used in Operation Warp Speed contracts, the (vaccines) products it commissioned "amount to bioweapons".

The US military defines a biological agent as a micro-organism (or toxin derived from it) that causes disease.

Vaccines are regulated by the US Food and Drug Administration as biological products, therefore they can be described as biological agents.

The mRNA (ModRNA) products instruct recipients cells to make a form of its spike protein, the most antigenic and, some researchers argue, toxic part of a coronavirus.

Since December 2020, 5.5 billion people, 72 per cent of the global population, have been injected with Covid-19 vaccines commissioned under Operation Warp Speed by the US Army "as countermeasure prototypes", by 2024 at least 8 billion people out of 8.5 billion people have been vaccinated with these bioweapons.

By the US military's own definition, The US Army Covid-19 vaccines bioweapon provides "the objective of a countermeasure which is the impairment of the operational effectiveness of enemy activity" by spike protein,the most antigenic and toxic part of a coronavirus,as a weapon,is proven,but for the vaccinated, they are the vaccine experiment then.

Trump followed on by Biden. Excuse me for saying so, but after the world populations have been decimated down to 250 million, more or less by 2025/26, by this US Army bioweapon, who will be left to use it on?

Refer back to the beginning of my above article and read it again, if you missed something, from my "Update 2".

I can't help wondering if the Elite, comprising Putin, Trump, Biden, Xi and other world leaders and the unseen billionaires, the WHO, WEF, etc, are in this together, but playing their parts to make we, the "Human Rubbish" of their societies, think there are warlike political divisions between us, when those divisions are for "your" show, just to fool you, while your extermination continues unregulated.

It is what I've been saying in my substack these past 4 years, I just never had the facts to prove my theories, now I do.

Whoever you are, wherever you work, vaccinate the Elite in your sphere but leave theit Human Rubbish who we are, alone.

PROOF: US Military Involvement:

stockpiled for use in the event of a bioterrorism attack. Kadlec later worked for Emergent Biosolutions as a consultant and in 2014 both companies helped fund the Bipartisan BioDefense Commission he founded.

In 2006, Kadlec helped create PHEMCE, the Public Health Emergency Medical Countermeasure Enterprise, to oversee the \lquote research, advanced development, procurement, stockpiling, deployment and utilisation of MCM\rquote during \lquote intentional, accidental or natural\rquote public health and medical emergencies. The US Department of Health and Human Services (HHS) oversees PHEMCE in conjunction with US DoD, Veterans Affairs, Homeland Security, the Department of Agriculture and as of 2019, the Director of National Intelligence. While Kadlec served as HHS\rquote s Assistant Secretary of Preparedness and Response (ASPR) he was PHEMCE\rquote s co-chair. PHEMCE is now co-chaired by the Director of the White House Office of Pandemic Preparedness and Response Policy (OPPRP). The Director is a former DoD official, Major General (Ret) Paul Friedrichs. The position itself was a new office created in 2022 by Congress.

The Biomedical Advanced Research and Development Authority (BARDA) is the agency within HHS that delivers PHEMCE, working with \lquote industry partners\rquote and funding the development of civilian medical countermeasures. Essentially, US government financing de-risks the development of these products by private companies, which the government then purchases and stockpiles. As HHS states in the current PHEMCE budget: \lquote Although these MCMs may not have FDA approval at the time of initial delivery to the SNS (strategic national stockpile), they may potentially be used under investigational drug protocols, such as clinical trials or may potentially be used under the FDA provisions for Emergency Use Authorization (EUA).

Under the legislative provisions for EUAs, it is the Secretary of Health and Human Services who directs the FDA to issue one. In another recent interview with Clayton Morris of Redacted, Latypova called the FDA oversight of the clinical trials a theatrical performance.

\lquote There\rquote s a law on the books, 21-USC-360bbb, that says, \ldblquote Emergency use authorized countermeasures under public health emergency cannot constitute clinical investigation.\rdblquote If clinical investigation is not possible, then you cannot have clinical trials, you cannot have informed consent, you cannot have clinical trial subjects, or clinical trial investigators,\rquote she said, explaining that the pharmaceutical companies had been commandeered to produce the non-Good Manufacturing Practice compliant injectables.

\lquote People were never told \ldblquote come over and get injected with countermeasure prototype\rquote , were they? People were told, this is a vaccine. It\rquote s safe and effective. It\rquote s been tested rigorously,

said Latypova. By the way, no testing of safety has been done. They have not done any animal trials, not even started them before they started mass injecting people in human trials, and that\rquote s a complete violation of all regulations everywhere in the world, including FDA [the US Food and Drug Administration]. They just went straight into people.

In practice, the distinction between BARDA\rquote s civilian-focused work and the military countermeasure projects overseen by the US military\rquote s Defense Advanced Research Project Agency (DARPA) is becoming increasingly moot. In July 2019, Kadlec appeared in place of BARDA\rquote s Director Dr Rick Bright at the Biodefense Commission \lquote Manhattan Project\rquote forum saying, \lquote We\rquote re working to integrate our portfolios with DoD, to make them a co-chair on the emergency counter measures enterprise, PHEMCE. But it\rquote s the whole notion that we can do things better when we work together and there\rquote s a pattern of this already. Zmapp [a drug used to treat Ebola] and the Merck Ebola vaccine were all products of the DoD early pipeline that were transferred to BARDA to basically move them forward. And so I think there is a process here that is being expanded beyond these onesies and twosies that were done under the situation of an emergency [the Ebola PHEIC] which was in 2014, that we can routinize to basically do it across a domain to look at these kinds of products.

Kadlec was no longer content with the occasional BARDA-sponsored product being authorised and had grander plans for new standard operating procedures. In 2020, Operation Warp Speed (OWS) was the vehicle he used to accelerate the PHEMCE enterprise, a big bang intended to expand the number of vaccine technologies in use. Kadlec told the Biodefense Commission that his Scientific Wild Assed Guess (SWAG) was that a biodefense Manhattan Project would cost $20-30billion. In the end the US government spent $18billion. President Trump said he invoked the Defense Production Act more than 100 times to facilitate OWS.

Pfizer\rquote s $1,950,097,500 Operation Warp Speed contract with the US government is a letter of direction issued by the US Army to demonstrate its \lquote capability to manufacture 100million doses of its currently unapproved mRNA COVID-19 vaccine for the government\rquote . mRNA vaccines are a technology the military wanted for its Inner Armour rapid response vaccine programme. The prime contractor is classified as a \lquote non-traditional defense contractor\rquote . In addition, it was given absolute liability indemnification for making medical countermeasures against SARS-CoV2 through a February 4, 2020 declaration under the Pandemic Response and Preparedness (PREP) Act issued by the HHS Secretary Alex Azar. Kadlec drafted the PREP Act in 2006 when he was staff director of the Senate HELP (Health, Education, Labor and Pensions) Committee.

Pfizer were responding to a US Army \lquote Request for Prototype Proposals\rquote for \lquote COVID-19 Pandemic \f1\endash Large Scale Vaccine Manufacturing Demonstration\rquote issued to members of the Medical CBRN (Chemical, Biological, Radiological & Nuclear) Defense Consortium (MCDC). The consortium was established by the US government after Congress expanded the scope of a provision of the National Defense Authorization Act enabling Defense agencies to use a fast-track contracting mechanism called Other Transaction Authority previously limited to the acquisition of weapons and weapons systems. MCDC\rquote s purpose is to \lquote support the DoD\rquote s medical pharmaceutical and diagnostic requirements as related to enhancing the mission effectiveness of military personnel\rquote . Pfizer\rquote s base contract with the MCDC dates to 2018.

The US military defines a biological agent as a \lquote micro-organism (or toxin derived from it) that causes disease\rquote . Vaccines are regulated by the FDA as biological products, therefore they can be described as biological agents. The mRNA products instruct recipients\rquote cells to make a form of its spike protein, the most antigenic and, some researchers argue, toxic part of a coronavirus.

Since December 2020, 5.5billion people, 72 per cent of the global population, have been injected with Covid-19 vaccines commissioned under Operation Warp Speed by the US Army as countermeasure prototypes. Evidence is mounting that these OWS vaccines are ineffective at countering the virus while evidence simultaneously mounts linking them to increases in the incidence rates of cancer and cardiac diseases. The novel technologies used were hastily fast-tracked into human trials while Operation Warp Speed received material assistance from the UK Medicines and Healthcare products Regulatory Agency (MHRA) who recklessly authorised them. By the US military\rquote s own definition, the objective of a countermeasure is \lquote the impairment of the operational effectiveness of enemy activity\rquote . The injection of these countermeasure prototype vaccines which satisfy the US military definition of a biological agent into people has killed some recipients and permanently disabled increasingly large numbers of others, resulting in their \lquote operational effectiveness\rquote as human beings being impaired. Even if it was not its intention, based on the measurable effects of their deployment, by the US military\rquote s own definitions of terms used in OWS contracts, the products it commissioned amount to bioweapons.

https://www.keionline.org/misc-docs/DOD-ATI-Pfizer-Technical-Direction-Letter-OTA-W15QKN-16-9-1002-21July2020.pdf

You will find Operation Warp Speed mentioned in that contract, in the 3rd paragraph down -

What was the sum paid, translated into words, as my educational ability does not stretch that far - but the US Army apparently, supplied the World, as well as "just America".

It was the US Army who packed up and removed the Fort Dettrick Level 4 BioLab after Gates Event 201 - Moderna's Covid-19 virus was released a few weeks later - and the US Army took the BioLab away at night in a fleet of US Army trucks, according to locals.

It is the US Army which is managing the Genetic Modified Super Soldier program, as a follow on from after the Gene Therapy Injections (GMO's) for those suitable, who survive the vaccines, presumably.

It would probably have been the US Army who would have the Ground Based Energy Weapon used in Hawaii recently, to remove and modify the area, for new building construction, etc.

The US Army distributed the Pfizer vaccines to all bases around America for distribution into the arms of the willing and to the Military of other countries too - for what essentially seems to be your Euthanasia program, thanks to the now injected Spike Protein Factories, in all of your Organs and Blood, which, when they start producing Spike Proteins, possibly by 5G signal, to your new injected MAC address, cause your body to start attacking itself, causing your quick death, by Turbo Cancers or some other dreadful disease, an eventual process which cannot be stopped.

Find your MAC address with Apple: BT Explorer. Android: Inpersona - or both with Bluetooth.

The end result expected, to achieve a world population, down from 8.5 billion down to 250 million within the next few years and on target to achieve that, according to Deagles, better known as "The Great Reset" which you have volunteered to be part of by agreeing to be vaccinated (it only applies to the vaccinated)- a lot more info you can find on my substack - by the Billionaires who pull Trump's strings and to whom he is currently beholden (well one of them). Trump or for that matter Biden who continued where Trump left off, for President again - much laughter, really?

Globalist billionaire Bill Gates has been caught telling his inner circle that a devastating “global famine” is the next step in the elite’s indomitable march towards total global domination.

The 500 million souls left on Earth following the great depopulation (my source says 250 million, but they can't just stop the depopulation by vaccines injection, like turning off a tap, can they) will not only be easily controlled, according to Gates, they will also yearn for the level of control that the elites can currently only dream about.

With total control of the food supply, farm land, seed banks, and genetically modified soil microbes, Gates has positioned himself to carry out a false flag worse than 9/11.

The New York Times apparently published a few days ago (10th June 2024) that the Covid-19 virus escaped from an American BioLab (from 2013 when it was created and when it was patented by Moderna) and not from China at all - well I've known and published that on my substack for years - read on.

Donald Trump's tenure as the 45th president of the United States began with his inauguration on January 20, 2017, and ended on January 20, 2021. Wikipedia - note "2017-2021"

DARPA has openly bragged on Twitter that Moderna’s mRNA vaccine technology, and by extension Moderna’s Covid vaccine, was a product of their ADEPT program, however, research shows that Moderna did not merely apply for a patent in 2016 with US9587003B2: as reported in the Daily Mail. They actually applied in 2013 for 4 patents with US9149506B2, US9216205B2, US9255129B2, US9301993B2, as well for their “Covid-19 virus” patent #CTCCTCGGCGGGCACGTAG

ADEPT is a Defence Advanced Research Projects Agency (“DARPA”) program that began in 2012. The acronym stands for Autonomous Diagnostics to Enable Prevention and Therapeutics. PROTECT is a sub-program of ADEPT, and it stands for Prophylactic Options to Environmental and Contagious Threats

The Johns Hopkins Center for Health Security in partnership with the World Economic Forum and the Bill & Melinda Gates Foundation will host Event 201: a high-level simulation exercise for pandemic preparedness and response, in New York, USA, on Friday 18 October, 08.45 – 12.30 EDT 2019

Moderna's Patented virus #CTCCTCGGCGGGCACGTAG patented 2013, was released a few weeks after Bill Gates Event 201 (about November 1st 2019) and the BioLab at Fort Detrick was dismantled and taken away in a fleet of Army trucks at night, according to residents who were living there at the time.

Let’s start by looking at the confidential agreement proving Moderna had a Coronavirus vaccine candidate "at least nineteen days" before the alleged emergence of SARS-CoV-2 in Wuhan, China - 1st January 2020.

The confidential agreement states that providers ‘Moderna’ alongside the ‘National Institute of Allergy and Infectious Diseases’ (NIAID) agreed to transfer ‘mRNA coronavirus vaccine candidates’ developed and jointly-owned by NIAID and Moderna to recipients ‘The University of North Carolina at Chapel Hill’ on the 12th December 2019.

NIAID, via Eco Health Alliance, clearly funded the creation of SARS-CoV-2-WIV. They are at least partially responsible for the millions of deaths that this genetically modified virus caused. NIAID has been involved in gain-of-function work with influenza that was so dangerous that it triggered the Obama administration to put a hold on gain-of-function research to 2017, in other words:

"Obama shut the NIAID down".

Barack Obama's tenure as the 44th president of the United States began with his first inauguration on January 20, 2009, and ended on January 20, 2017. Wikipedia

"which was lifted under Trump's administration 2017-2021", in other words:

"Trump let the NIAID out"

Fort Detrick is the army base that hosts USAMRIID, which is located in Frederick, Maryland - just outside of Washington DC. From 1943 to 1969, it was home of the US Biological Weapons Program. Once that was disbanded, it became the US DoD “biological defense” program. Under that program, some of the world’s most dangerous pathogens, such as Ebola, Anthrax and Smallpox, have been experimented with at that location. It also stored some of the world’s most dangerous pathogens. In the early 2000s, it was at the center of the weaponized anthrax attacks. The government concluded early on that Fort Detrick was where those anthrax spores were derived from, although there is contradictory evidence suggesting an alternative source involving a large non-profit contractor company which does a lot of business on behalf of the NIH/DoD/”Biodefense” industrial complex.

Dr. Redfield served as the director of the CDC from March 2018 to January 2021. In that role, he made what he called the most difficult decision of his long career, and shut down Fort Detrick in August 2019. It stayed shuttered until April 2020. Fort Detrick is the largest employer of Frederick County, MD, so it was a very big deal. Dr. Redfield shut down the US biological defense program at Fort Detrick because of a pattern of repeated failed safety violations that he says placed the citizens of Frederick, MD at great risk. Many of us have speculated for years just exactly what that risk was. The whole episode was shrouded in mystery, but my understanding at least partially involved a new research laboratory designed to house non-human primates within which Ebola experiments were planned. At least one of the issues involved problems with air handling, reminiscent of one of the key issues that cropped up at the Wuhan Institute of Virology.

Fast forward to the latest revelations by Congress (from the House Energy and Commerce Committee press release).

The House Energy and Commerce Committee today released a report titled “Interim Staff Report into Risky MPXV Experiment at the National Institute of Allergy and Infectious Diseases.”

The report details the Committee’s investigation, which was launched following a 2022 Science magazine interview in which Dr. Bernard Moss of the National Institutes of Health’s (NIH) National Institute of Allergy and Infectious Diseases (NIAID) revealed that he was planning to insert segments of a lethal strain of MPXV (formerly known as “monkeypox”) into a more a transmissible strain of the virus. This proposed experiment alarmed some scientists concerned about the risks of creating an enhanced version of the MPXV virus.

For nearly a year and a half, the Department of Health and Human Services (HHS), the NIH, and NIAID misrepresented and deceived the Committee by repeatedly denying that the potentially dangerous experiment was proposed and approved. However, after being pressed repeatedly by Committee Leaders, HHS ultimately admitted Dr. Moss’s research team had been granted approval to conduct a bidirectional MPVX gene-transfer experiment (i.e., inserting the more lethal strain into the more transmissible strain and vice versa). Documents made available for review to Committee staff confirmed the 2015 approval of the experiment and raised additional concerns.

HHS, the NIH, and NIAID still maintain the riskier research project was never conducted. However, no documentation or any other evidence has been produced to substantiate the claim. NIAID has also failed to offer any explanation of the circumstances and rationale that supposedly led the Moss research team to drop the bidirectional mpox gene-transfer experiment after receiving approval for the project.

The report concludes with a series of recommendations related to biosecurity to ensure future transparency and accountability related to risky research like this.

This documents that, in the case of NIAID, we have an institute that finds it acceptable to lie and obfuscate to Congress, and so far, there is no accountability other than more Congressional investigations. All of this reeks of an institutional culture of chronic arrogance, entitlement, and disregard for fundamental biohazard safety considerations.

Dr. Bernard Moss, the scientist at the heart of this controversy, has not been subpoenaed, nor has his scientific staff that we know of. There is no question that gain-of-function work was performed, and relatively recently, too. The only question is how far did these experiments go.

On October 28, 2022, Science magazine made a clarification to its October 19, 2022, article based on information provided by the NIH. The clarification stated explicitly that the clade II virus in Dr. Moss’ research discussion in the September 2022 Science magazine was clade IIa, not clade IIb, which had spread in the U.S.40 The clarification did not refute that Dr. Moss had proposed or planned gene transfers from clade I to clade IIa. Further, Dr. Moss’ team wrote in an early November 2022 preprint of an article in the Proceedings of the National Academy of Sciences of the United States of America (PNAS) that later appeared in February 2023 that they intended to extend their research to include clade IIb: “We have started to investigate the genetic determinants responsible for virulence differences of clade I and IIa viruses and plan to extend this to clade IIb pending institutional approval.

NIAID, via Eco Health Alliance, clearly funded the creation of SARS-CoV-2-WIV. They are at least partially responsible for the millions of deaths that this genetically modified virus caused. NIAID has been involved in gain-of-function work with influenza that was so dangerous that it triggered the Obama administration to put a hold on gain-of-function research, which was lifted under Trump.

NIAID also funded H5N1 (avian influenza) gain of function research, which led to the moratorium on GOF research under the Obama administration.

NIAID is out of control. With a budget of 6.1 billion, it controls a vast empire for which there is no accountability and which actively stonewalls congressional oversight attempts.

NIAID has repeatedly failed to put Americans' safety first and foremost. NIAID has failed to put the safety of the citizens of the world first and foremost.

I am calling for a complete shutdown of NIAID. The current NIAID mission statement reads:

NIAID conducts and supports basic and applied research to better understand, treat, and ultimately prevent infectious, immunologic, and allergic diseases.

They have long since abandoned their core mission in favor of biologic “defense,” gain-of-function research, and doing the bidding of big pharma.

Since the start of the COVID-19 outbreak, NIAID has known it is at least partially responsible for the creation of the virus named SARS-CoV-2. It has had years to come clean and to fix its organizational and cultural issues. Instead, it has lied, obfuscated, and hidden the evidence of its responsibility for what happened. NIAID's organizational culture is arrogant and has a deep-seated sense of entitlement.

I propose that research at NIAID be shut down and the institute shuttered systematically and carefully. Of course, this must be done in a responsible manner - with biological tissue and pathogen banks being carefully preserved and assessed, but much of this archiving function is already outsourced to independent contractor companies.

Then, two new research institutes can be formed. One focused on infectious diseases, and the other on immunologic and allergic diseases. Leadership in these institutes should be completely replaced. The institutes should be focussed on what can work to provide benefit to the majority of Americans. The good example of how NIAID has ignored effective solutions being the use of Vitamin D with A, K, and zinc to boost the immune system. Another great example is how they have fought the use of generic drugs to fight infectious diseases despite a long track record of such drugs being effective in both the early and late stages of respiratory disease.

How to do this? Recently, President Biden and Congress founded ARPA-H. The same pathways that allowed this new institute to come to fruition can be used to start these two new institutes. The time to act is now, or at worst, certainly come January 20th, 2025.

Dr. Redfield showed true leadership in shuttering Fort Detrick/USAMRIID; it is time for the new President and Congress to do the same.

Above By Dr R Malone

This led WHO to declare a Public Health Emergency of International Concern (PHEIC) on 30 January 2020

The WHO characterized the outbreak as a pandemic on 11 March 2020.

AND WHO ordered "Disinformation Laws" to be put in place from "about" February 2020 to June 2023 with the help of your Government and the Politicians you voted into Politics, to force everyone to get their Covid vaccines.

Disinformation Laws take at least 18 months to pass into Law and be put in place, which means this pandemic was planned in 2017/18 for 2019/20 by WHO - you should ask the people you voted into Politics, what that timeline was, since they seem to be confused about whom they were supposed to serve, you, the Billionaires, or Big Pharma, who probably paid them big dividends, to betray you?

BionTech for Pfizer pirated Moderna's formula ”#CTCCTCGGCGGGCACGTAG and produced their own vaccines from it 2019/20, Moderna said on May 17 2024 that the European Patent Office had upheld the validity of one of the company’s key patents, a win in an "ongoing Covid-19 vaccine dispute" with Pfizer and BioNTech.

Pfizer paid the CDC (which Bill Gates funded) US$3.5 Million to release their vaccines ahead of Moderna's one and Moderna's vaccine candidate might not have been approved for injection by July 2020.

Bill Gates bought US$50 million Pfizer shares 9 weeks before his CDC approved the Pfizer vaccines, which Bill sold last year for US$450 Million - I wonder if Gates paid Tax on his profit of US$400 Million - if that's not "Insider Trading" I don't know what is.

Biden paid Bill Gates US$7.5 Billion about the same time, reason unspecified, worthy of explanation - but it was about the same time that Gates bought the large farmland parcel?

The US Army purchased Pfizers vaccines on 21st July 2020

DOD-ATI-Pfizer-Technical-Direction-Letter-OTA-W15QKN-16-9-1002- 21 July2020 (7.86mb)

https://www.keionline.org/misc-docs/DOD-ATI-Pfizer-Technical-Direction-Letter-OTA-W15QKN-16-9-1002-21July2020.pdf

The Department Of The Army US Army Contracting Command – New Jersey Picatinny Arsenal, New Jersey 07806-5000 for a Large Scale Vaccine Manufacturing Demonstration (Pfizer, Inc) for the total approved cost to the Government for $1,950,097,500.00

“JUST IN – Dr. Francis Boyle, the Harvard educated law professor that drafted the Biological Weapons and Antiterrorism Act of 1989, Provides Affidavit that COVID 19 mRNA injections are Biological Weapons and Weapons of Mass Destruction

Dr. Boyle stated that the COVID-19 injections violate Biological Weapons 18 USC § 175 and Weapons and Firearms § 790.166 Fla. Stat. (2023).

Covid mRNA Shots Are NOT Vaccines, Appeals Court Rules

Legal Precedent June 7, 2024 for U.S. Citizens to Deny Medical Treatment.

June 7, 2024: The 9th Circuit Federal Court of Appeals just ruled held that “[t]his misapplies Jacobson,” which “did not involve a claim in which the compelled vaccine was ‘designed to reduce symptoms in the infected vaccine recipient rather than to prevent transmission and infection.”’ Jacobson does not, the majority concluded, extend to “forced medical treatment” for the benefit of the recipient.”

When HFDF asked the court to opine as to whether or not the CDC’s claim that the COVID-19 vaccines were ‘safe and effective’, the court responded with the rhetorical question, “safe and effective for what?”

But here is a problem - future vaccines are now as per ”June 7, 2024: The 9th Circuit Federal Court of Appeals just ruled are "forced medical treatment" and the CDC’s claim that the vaccines are ‘safe and effective’, the court responded with the rhetorical question, “safe and effective for what?” which makes all "vaccines" illegal, by definition and purpose.

Legal Precedent June 7, 2024 for U.S. Citizens to Deny Medical Treatment.

A Legal Precedent is a Legal Instrument which is supremely powerful because it is a ruling by a Judge, which changes the "Legal Nature" of an issue by Law and it is the mechanism by which a Judge, anywhere, can issue a Judgement, on any legal proceeding, which predetermines a vaccine, as actually being a "forced medical procedure" and nothing else.

“forced medical treatment” , “safe and effective for what?”

https://slaynews.com/news/covid-mrna-shots-not-vaccines-appeals-court-rules/

VIDEO - Absolute Truth with Emerald Robinson and Dr.David Martin - 9th Circuit Court rules COVID-19 mRNA Injections are not "Vaccines"

Like going to your Sales Representative for Big Pharma Doctor, to get an ingrown toenail removed - another forced medical treatment perhaps?

If Hillary Clinton had become US President and not Trump (By defaulting Hillary to win the swing voters), Trump's inauguration January 20, 2017, then with Bill Clinton's support, my guess is that this Covid pandemic would never have happened, which is why Trump should be sent to prison, for dishonestly acquiring the last Presidency by Criminal Default, convict which he has now become, because of it - and his deliberate vaccines policy as above and the Army Contact you must download as a PDF for verification.

At the run up to the 2017 Presidential Election there was only Trump and Hillary, as you will recall. Trump said he was going to make "America Great Again", he just forgot to say how, but it seems with a "US Army Military Operation" at its core.

Not lost on me, is how little regard the Elite of our species have for the rest of us, who they call we, Ruman Rubbish, their willingless to get rid of us, by a freak of nature, which placed them in rich families, as babies and we in poor. Intelligence quota, about the same I'd say.

NIAID and Politics and Big Pharma at war with we the people, but universally?

But here is the joke: It does what no vaccine can do, it cures you of any virus: My FREE Salt Water Cure for Bird Flu and Covid and any other virus:

3 minutes from preparation to job done: Mix one heaped teaspoon of table (or Iodine) salt in a mug of warm clean water, cup a hand and sniff or snort the entire mugful up your nose, spitting out anything which comes down into your mouth. If burning sensation, then you have a virus, so continue morning noon and night, or more often if you want, until the burning sensation goes away (2-3 minutes) then blow out your nose with toilet paper and flush away, washing your hands afterwards, until when you do my simple cure, you don't have any burning sensation at all, when you flush - job done. Also swallow a couple of mouthfuls of salt water and if you have burning in your lungs, salt killing virus and pneumonia, there too.It washes behind the eyes, the brain bulb, brain stem (Long Covid), The Escutcheon Tubes to the inner ears and the top of the throat which is at a point roughly level with half way up your ears and not where your mouth is and it goes down the back of your throat, when infected there too.

I have been doing this simple cure for over 31 years and I am and others, never sick from viruses and there is no reason why any of you should be.

Simply put, if the inside of your nose is dry and crusty, you are OK, if your nose is runny, you really need to do a salt water sniffle as quickly as possible AND THERE IS STILL CLEAN SEA WATER, TO USE INSTEAD.

Nobody has been injured or killed by my above salt water cure