Archive for the ‘vaccines’ Category

URGENT: H.R. 550 – the End of Freedom as We Know it – What You Need to Know About “Vaccine” Passports & Tell OSHA to Kill Mandatory “Vaccines”

https://standforhealthfreedom.com/blog/hr550mythsbusted/

Top 5 Myths Busted about the Immunization Infrastructure Modernization Act

HR 550 is a Wolf in Sheep’s Clothing

We’ve heard the term disinformation before. The Immunization Infrastructure Modernization Act, HR 550 is swimming in it. After sending out our last campaign to make people aware and activated about this bad bill, we received a ton of feedback from Advocates hearing back from lawmakers who supported the bill. The talking points were eerily the same. They also claim the opposite of plain language in this bill, like Orwellian Newspeak.

Before we dig into myth-busting this bill, it’s important to understand what the Immunization Infrastructure is. In short, it is the bones upon which a vaccine mandate could rest. An infrastructure ties together physical or digital components to create a framework and support system for an end goal. A common example would be a highway system—individual roads across states would be strengthened or built to combine into a seamless system for travel through the entire country. An infrastructure creates relationships between separate systems, like the Constitution did for our Colonies. When stakeholders like politicians and corporate philanthropists or contractors discuss the “immunization infrastructure,” as this bill is titled, they are talking about strengthening the systems already in place to get people vaccinated.

HR 550, is aiming to “modernize” already-in-place individual immunization registries, or Immunization Information Systems (IIS), as the databases are called. In this digital age, modernization calls from a federal (central) government mean standardization of tech and expansion of storage capabilities to get up to speed with the amount of data there is, how fast we want it to travel, and to where. This is why the bill explicitly states the $400 million for grants are to be given out only on the condition local IISs adopt CDC standards, including “interoperability” and “bidirectional” data transfer. This is the way the federal government makes its way into local policy and lawmaking—by conditioning federal handouts on compliance with federal policy. It’s passive aggressive bullying with our tax dollars.Everyone gets this nice thing, except for the people who don’t do what I say.” To illustrate, the drinking age is 21 in every state, despite it being state law, because that age was tied to federal funding for highways. The federal government doesn’t have to make a law about local rules (that would be fought as overreach) if they simply give out money conditioned on compliance.

IISs are older than HIPAA. They sprung up when EHR (electronic health records) were being developed in the 70s were adopted faster. IIS and EHR are separate systems, but they intertwine. IIS are “local” to a geographic area like a state, but they were an initiative of the CDC, along with funding from the Robert Wood Johnson Foundation, to address concern that children weren’t getting all the ACIP vaccinations. So, in essence, one could say, the first health metric the government worked on tracking digitally was vaccine use. The technology for a large, multi-jurisdictional centralized database wasn’t yet available, so the CDC funded states to set up their own.

Here is the CDC’s strategic plan for “local” IISs, as laid out in 2017:

IIS Vision: Real-time, consolidated immunization data and services for all ages are available for authorized clinical, administrative, and public health users and consumers, anytime and anywhere.

IISSB Mission: Maximize protection against vaccine-preventable diseases by leading the advancement of immunization information systems (IISs).[i]

Very clearly, the IISs are the data arm (infrastructure) of a federal plan to vaccinate as many people as possible.

Myth #1: This Act would NOT create a federal vaccine database or tracking system.

It doesn’t have to. That infrastructure is already in place and under development. (In fact, one would wonder if instead of a centralized database, the technology might be pointing in the direction of a decentralized blockchain data system.) There is no need for a bill to create a central federal database. Instead, this bill would link everything together under CDC oversight. From the horse’s mouth: “IISs have matured individually…However, IISs are increasingly viewed as one national network of systems.”[ii]

What this bill would create is more access for CDC for your immunization data, and the need for states to follow CDC recommendations or get cut off from federal funding. Does data access have to be centralized to be an invasion of privacy and federal overreach? No. “The present pandemic is the first time near real-time vaccination data has been shared with the CDC to provide comprehensive surveillance at the federal level. These data are primarily coming from IIS.” This statement was testimony by Rebecca Coyle, Executive Director of the American Immunization Registry Association (AIRA), which promotes development and implementation of IIS around the country along with close collaboration with the CDC. She continued, “The Immunization Infrastructure Modernization Act, HR 550, legislation by Representatives Annie Kuster and Larry Bucshon will provide the needed national framework for IIS operations.”

The bill itself states the HHS Secretary shall support adoption of the IIS standards of the CDC. The Secretary shall enhance capabilities of IIS “to evaluate, forecast, and operationalize clinical decision support tools in alignment with the recommendations” of the ACIP, a federal advisory committee with no public accountability, which states are not mandated to follow, but would be required to “operationalize” if they receive grant money under this bill. Does this language mean if a state does not follow the ACIP childhood or adult immunization schedules, the state would be disqualified from grant money from the federal government? That isn’t explicitly stated in the bill, but it wouldn’t be prohibited either. The language of the bill as passed by the House begs that question. Since the $400M can go to either localities with IIS, or public-private contracts for implementation, for argument’s sake, let’s say that money is divided equally and 50 states could apply for $200M. That approximates $4M per state to “modernize” their IIS. (Federal grants never work this cleanly, but this is a thought exercise.) What state will turn down $4M in federal money to update health data technology, especially during a “pandemic”?

The National Adult Immunization Plan notes that “IIS have the potential to act as a centralized repository of adult vaccination records.” NAIP strategy includes “expand[ing] IIS and EHR functionality to facilitate interstate immunization data exchange through a centralized hub.” The Plan also tells us the Office of the National Coordinator for Health Information Technology in HHS is working on a national “data hub” to enable “state and local IIS to exchange data with each other through a centralized model…By connecting to the central hub, jurisdictions can then connect to any other jurisdiction also connected to the centralized hub.”

HR 550 does not mention this centralized data hub. But Plans and documentation from the agencies charged with carrying out HR 550, along with stakeholders like AIRA, have been talking about it for a long time.

“Public health agencies have been using IIS for more than twenty years to consolidate a complete immunization record for the people within their jurisdictions, and to provide that data to authorized users through standardized, electronic means.”[iii]

Myth #2: This bill increases privacy of immunization records.

The main sponsor of the bill, Democrat Annie Kuster from New Hampshire, introduced the bill by noting the IIS system is used “to remind patients when they are due for a recommended vaccine.”[iv] This is also a stated goal of the National Adult Immunization Plan. What kind of privacy is that?

Rebecca Coyle, Executive Director of the American Immunization Registry Association, testified in front of the House Energy & Commerce Health Subcommittee in June 2021 that “At the point of clinical care, an IIS can provide consolidated immunization histories to determine appropriate patient vaccinations for use by a vaccination provider.” There is no way that can happen with deidentified data. The data must be linked to the individual in a multi-jurisdictional way, for the immunization history to be displayed in an electronic record for an individual who may go to different providers, move to different states, change names through things like marriage, etc. Remember, the CDC encouraged states to adopt their own IISs because they wanted more children vaccinated. How can you vaccinate more children based on collected data if you don’t know who is vaccinated (and when, and how many times) and who is not? The point of the system is to collect individualized data so government can get individuals vaccinated at the “point of clinical care,” meaning when an individual is in a doctor’s office. You don’t get much more private than that. The data collected by IIS is not simply “population level.” It is individually identifiable information. The federal government can claim they can’t or won’t access that information. Do you trust that? Why would the sponsor of the bill crow about the individualized capabilities of the system if the federal government isn’t going to have access to that?

Section (a)(1)(B)(vi) of the bill states the HHS Secretary shall support adoption of the IIS functional standards of the CDC “and the maintenance of security standards to protect individually identifiable health information as defined in section 160.103 of title 45 CFR.” States have their own privacy provisions for their own IISs, but this section tells the HHS Secretary to support adoption of federal security standards for PHI as explained in the Public Welfare Code. There, PHI is defined as “individually identifiable health information” except that which is covered by FERPA, the Family Educational Rights and Privacy Act, and “in employment records held by a covered entity in its role as employer.” So the security standards to be adopted exempt certain educational and employer records from HIPAA entities from privacy law.

Myth #3: This bill reigns in reckless Democrat spending.

There are claims that this bill will reign in the distribution of $500M from the Democrat-backed American Rescue Plan allocated for upgrades to IIS, “without guardrails.” However, this bill allocates $400M for the HHS Secretary to give out at his discretion for localities to modernize (or initiate) their IIS structure, or for public-private contracts to facilitate the same. There is nothing in this bill that modifies the American Rescue Plan.

Myth #4: This bill was Republican-led.

The bill was introduced by Democrat Annie Kuster from New Hampshire on January 28, 2021. Republican Larry Buschon signed on as an original cosponsor. There are 13 other cosponsors, 3 Republican. All House Democrats voted for this bill along with 80 Republicans; 130 Republicans voted against and 3 abstained. This bill is bipartisan at best. To say it is Republican-led is misleading.

It would be more accurate to say the opposition is Republican-led.

Based on a reading of the bill, and a knowledge of the history of the federal efforts for an immunization infrastructure, the Republicans who voted yes on this bill are either recklessly uninformed, or knew exactly what they were doing and are now selling the public an Orwellian bill of goods. Neither is good.

Myth #5: This bill has nothing to do with unconstitutional federal vaccine mandates or a digital health pass.

This bill has everything to do with mandates and digital health passes. It is the legal infrastructure, so to speak, for the digital infrastructure. At this point, most of the immunization data collection is local. The federal government is not collecting it directly and needs to rely on localities to pass it along. The technology for mass health data collection and transfer of that information is still evolving and was certainly not in place in the 70s when the digital groundwork was being laid for IIS. Vaccine passports are still in development and one of the hurdles is access to information. At this moment, the Biden Administration is asserting they would not support digital passports, but president-Elect Biden also stated he did not think the federal government should mandate vaccines until he changed his tune in office. And if the White House changes their mind on passports as well, HR 550 is exactly the bill they would need to make it legit through the legislative process, rather than facing legal challenges for federal overreach as they are now with mask and vaccine mandates through arms like OSHA and CDC.

The CDC has been exploring “Smart Health Cards” along with AIRA and private organizations for years. Here’s an excerpt from a recent Discovery Session:

“AIRA, as well as several member and partner organizations, have signed on as VCI with the belief that IIS can and should play a significant role as issuers of digital or paper vaccine credentials, and that broader consumer access to immunization information supports health equity and empowers individuals to share their health information as they choose.”[iv]

Additional Resources

Below is a great summary of H.R.550 from Dawn Richardson’s perspective. Dawn is the Director of State Advocacy for National Vaccine Information Center (NVIC) and has a show “Advocacy Lifeline,” on CHD TV, every Monday at 2:30pm. Tune in to hear her perspective of the bill starting at the 3 minute and 30 second mark.

Untitled Presentation 169 e1639162811477

Steps You Can Take

Step One: Tell your lawmaker to vote against HR 550. We do not want vaccine mandates and digital passports. Click below!
 
 
Step Two: Share the information! Truth is hard to come by in these days. Shout it from the digital mountaintops! Click the links on the left side of the page to spread the good word.
References & Sources

[i] 2018-2020 CDC Immunization Information System Strategic Plan, Oct. 1, 2017

[ii] https://hln.com/vaccine-credential-activities-redirecting-the-conversation-for-public-health-registries/

[iii] 2018-2020 CDC Immunization Information System Strategic Plan, Oct. 1, 2017

[iv] https://mustreadalaska.com/don-young-joins-bipartisan-group-to-approve-national-vaccine-database-bill-hr-550/

[v] https://repository.immregistries.org/resource/aira-discovery-session-vaccine-credentials/

___________________

From Children’s Health Defense:

On November 30, H.R. 550, a federal bill passed in the U.S. House of Representatives. 

The bill, “Immunization Infrastructure Modernization Act of 2021,” would expand state and local health department vaccine-tracking systems to monitor the vaccination status of American citizens. States would provide the information to the federal government.

The bill may be difficult to stop as it already has bipartisan support. It passed the House with the support of 294 U.S. Representatives, including all Democrats and 80 Republicans.

H.R. 550 is now under consideration by the U.S. Senate where, if passed, it could be implemented in under 12 months.

H.R. 550 would lead to a monumental invasion of our rights as American citizens. It would set an incredibly dangerous precedent and could lead to more vaccine mandates, and more restrictions of services and healthcare for the unvaccinated.

The bill also creates a mechanism for federal, state and local governments to enforce vaccine passports and possibly no-fly lists. And it would be costly to taxpayers — it appropriates $400 million dollars to expand vaccine tracking.

Part of this money would be spent on grants and cooperative agreements to state or local governmental entities that agree to adopt the new data collection guidelines set by the Centers for Disease Control and Prevention.

It’s imperative that we work to educate our Senators on why this legislation poses an unprecedented threat to freedom and liberty, and how it will lead to an unconstitutional invasion of privacy and loss of medical freedom.

Once freedoms are lost, they’re nearly impossible and extremely costly to regain through legal action. The time to act on this is now!

Please take a few moments to complete this action alert by simply entering your name and address, and a letter explaining why you oppose this legislation will automatically be sent to your federal representatives.

And mark your calendar now, to put aside time on Monday, December 13 to call your elected representatives. To make it easier, we’ve included a brief phone script. Calls to voice your concerns for any legislative matters are the most effective way to influence representatives, so please make the time to do this!

This is an invasion of privacy and freedom that no American citizen should be comfortable with and it’s critical that we all take action now! Thank you for taking the time to help us defend our freedoms and restore democracy.

TAKE ACTION

Contact both of your U.S. Senators and tell them why you oppose H.R. 550. You can send the letter below to them via email by filling out the form provided. Then use this site to locate your two Senators’ their phone numbers and call both of them.

Here’s a sample script:

“Hi, my name is ____ and I am a constituent. I am calling to tell Senator ____ my views on H.R. 550, which would unnecessarily appropriate hundreds of millions of dollars to expand vaccine tracking systems. This is an unprecedented invasion of the medical privacy of American citizens. This bill violates the traditional principles of consent for sharing an individual’s medical information. It’s bad enough that many state and local departments share our health data without our consent, but now they would be sharing our data with the federal government also. Adults are fully capable of keeping their own and their children’s vaccine records. Americans should never be required to allow the government to access their private medical information. I urge the Senator to stand up for medical freedom and protect Americans’ medical privacy; especially for those individuals in our state.

If the form is not working for you, try this page.

____________________

https://besovereign.com/health-freedom-advocacy-center/stand-for-health-freedom-753?  Video Here (Approx. 48 Min)

“Vaccine” Passports

A world where we accept digital identities, is a world where our children and their minds are commoditized. Digital identities limit privileges and mobility in the world, including well beyond medical decisions. Selling bodily autonomy to big tech and big industry comes at a great cost to our children and to our ability to be a good relative.

Alison McDowell is a mother, writer, former teacher and dedicated investigative researcher & has rare insights on what is actually happening in the world from a systems point of view. Her level of awareness empowers everyone who listens to step through this historical and critical time as a free and sovereign individual.

Listen here to Dr. Naomi Wolf discuss mandatory “vaccination” for 5 years old and up by Dec. 27, 2021 in New York, who warned us about “vaccine” passports previously.  New York has become a “prison state.”

Please also view this important video where Melissa Ciummei, a financial investor from Northern Ireland, has serious concerns that injection passports will be used more like data passports to control participation in society.  She believes that this passport system was manufactured in order to help bring about a financial reset, replacing our failing fiat currency system.  Because passports are so crucial for the successful implementation of this new financial system, mandatory “vaccination” of all citizens, young and old, will be imperative for the plan to succeed. It’s all about the financial system and has nothing to do with health.  She states we are very close to data passports due to compliance. Here, she discussed the real reasons for the lockdowns.

Remember patent #WO2020060606, owned by Microsoft employees which is described as a “Cryptocurrency System Using Body Activity Data,” and senses body activity of the user?  The patent states that “conditions set by the cryptocurrency system” can be awarded cryptocurrency to the user. In other words, if you are a good boy or girl you get points.  But, what happens if you aren’t a good boy or girl? Points, money, and privileges can be taken away.

I posted about Gates’ push for “vaccine” tracking here:

These ‘digital certificates’ are human-implantable ‘QUANTUM-DOT TATTOOS’ that researchers at MIT and Rice University are working on as a way to hold “vaccination” records. It was last year in December when scientists from the two universities revealed that they were working on these quantum-dot tattoos after Bill Gates approached them about solving the problem of identifying those who have not been vaccinated.

The implantable mark emits a glowing red X pattern as it delivers the vaccine and what is left behind is capable of data storage and retrieval for years afterwards.  Smartphones are implicated:

“Detection of the microdots is possible using specially adapted smartphones that can detect the near-infrared fluorescence. ‘Because these phones offer on-board processing power, camera applications, and inexpensive consumer-grade camera modules, we chose to adapt an existing smartphone to enable NIR imaging rather than build a completely new imaging system,” they wrote. “In addition, we believe that familiarity with the function of these devices will lessen the learning curve for NIR imaging in a field setting.’”  https://www.genengnews.com/topics/drug-discovery/quantum-dots-deliver-vaccines-and-invisibly-encode-vaccination-history-in-skin/

Researchers have turned this technology to the COVID-19 virus.

A 2019 MIT study funded by the Gates Foundation describes how “near-infrared quantum dots” can be implanted under the skin along with a “vaccine” to encode information for “decentralized data storage and bio-sensing.”  https://sci-hub.tw/10.1126/scitranslmed.aay7162

All of this stored data needs to have a system big enough to handle it.  Enter 5G.

Hopefully, for anyone still in denial, it is becoming clearer all the time what COVID-19 is really about.

DO NOT COMPLY.

For more:  https://madisonarealymesupportgroup.com/2020/04/25/coronavirus-science-policy-politics-5g/

______________________

https://childrenshealthdefense.org/defender/action-osha-end-mandatory-covid-vaccine-ruleemployers

Urgent Call to Action: Tell OSHA to Permanently End Mandatory COVID Vaccine Rule for Employers

The deadline is Jan. 19 for posting a comment asking the Occupational Safety and Health Administration to permanently suspend its Emergency Temporary Standard requiring employers with more than 100 employees to comply with President Biden’s COVID vaccine mandate.

The Occupational Safety and Health Administration (OSHA) on Nov. 16 suspended implementation and enforcement of its Emergency Temporary Standard (ETS) on mandatory COVID vaccination and testing in the workplace.

Under the ETS, employers with more than 100 employees were given until Jan. 4, 2022 to comply with President Biden’s COVID vaccine mandate.

However, a Nov. 12 ruling by the 5th Circuit Court of Appeals barred OSHA from enforcing the ETS “pending adequate judicial review” of a motion for permanent injunction.

Children’s Health Defense (CHD) is calling on all scientists, citizens and medical experts to ask OSHA to permanently end the ETS. Submit your comment today via the federal eRulemaking portal.

Follow the instructions on the website for submitting comments. Be sure to include the docket number — Docket No. OSHA-2021-0007-0001 — at the top of your comments. (Click here to view comments posted by others.)

After you post your comment, share this link with friends and family.

In its 22-page ruling, the 5th Circuit Court of Appeals called the Biden administration’s COVID vaccine mandate “fatally flawed” and said OSHA should “take no steps to implement or enforce the mandate until further court order.”

The court said the mandate fails to consider that the ongoing threat of COVID is more dangerous to some employees than others. These vaccines are experimental and potentially dangerous. According to the latest data released by the CDC, between Dec. 14, 2020, and Nov. 26, 2021, 927,740 reports of adverse events — including 19,532 reports of deaths — following COVID “vaccines” were submitted to the Vaccine Adverse Event Reporting System.

CHD believes it is critical that OSHA submit Environmental Impact Statements to the public on the safety, health and economic impact of its ETS.

Help stop OSHA’s ETS from becoming a final rule. Submit your comment today via the federal eRulemaking portal.

_________________

**Comment**

I realize writing a letter takes time, and in efforts of helping I’m sharing my letter for you to either use in full, or cut and paste to form your own.  OSHA letter

 

Dec. 15 Public Hearing Rescheduled For WI Senate 547, 662, 721 COVID “Vaccine” Bills

I was notified today by Senator Nass that the Dec. 15, 2021 public hearing has been canceled “due to the need to follow COVID protocols.” It will probably be rescheduled into early January. Stay tuned.

COVID “Vaccines”: What’s Really in Them? #RealNotRare Website For “Vaccine” Injured

https://childrenshealthdefense.org/defender/covid-vaccines-composition-proper-informed-consent

COVID Vaccines: What’s Really in Them?

The simple answer is we don’t know. We know what we’re being told is in them, but there is increasing evidence of big variations in the quality and composition of different batches, which may or may not be deliberate.

Topline:

  • Omicron is being used by governments and health authorities to mandate or coerce ever more people into receiving COVID-19 jabs.
  • It is imperative that sufficient information is given to potential vaccinees to allow properly informed consent. This article reviews key information that is not widely reported by governments, health authorities, vaccinators, the mainstream medical profession or the mass media.
  • Given that the most commonly used COVID-19 jabs rely on providing genetic information to the body to force it to produce a modified form of the spike protein, the jabs should not be represented as “vaccines.”
  • The mRNA jabs rely on genetic material that is significantly altered to generate mutant spike proteins that retain their prefusion conformity even after they get into cells. The lipid nanoparticles have not been adequately studied for their safety.
  • The viral vector jabs by AstraZeneca and Johnson & Johnson rely on human fetal cell lines and the majority of the protein in the jabs may be from this source, rather than from the viral vectors themselves.
  • The spike protein is toxic in its own right and may induce adverse effects on the body whether it is generated from genetic information from jabs or from naturally-acquired infection.
  • Contaminants, deliberate or accidental, have been found in many vial specimens.
  • There are no substantive data to justify the ‘safe and effective’ claims often made for COVID-19 jabs, especially not in the face of omicron.
  • COVID-19 jabs, especially if given repeatedly every few months, will likely cause lasting negative impacts on immune system function so increasing the risk of a wide range of other diseases while increasing risks of adverse reactions.
  • Clear evidence has emerged that data used for “vaccine surveillance” by the UK Health Security Agency (formerly Public Health England) has been accidentally or deliberately misrepresented to infer outcomes among the jabbed are better than for those who decline.
  • There is little or no evidence that informed consent is being, or has been, offered at any time during the “pandemic.”

Before diving into the detail, here is Rob’s short, 10-minute video summary:

Freedom on trial

Liberalism in Europe is not only under threat. It has in some parts already been extinguished.

As the first European nation to mandate COVID-19 injections, Austria will criminalize those who refuse the injections. Germany has since followed suit. Greeks will need to pay their government a monthly fee of €100 every month if they remain jab-free.

On Monday night Queensland-based medical doctor, Robert Brennan, told those of us attending the weekly World Council for Health meeting that doctors in Australia who are de-licensed for speaking out about lockdowns, testing or injection risks will be criminally charged for impersonation if they continue to use their doctor title.

We also heard more about the quarantine camps that are being set up, how indigenous populations are being targeted and how sacred sites are being destroyed under powers granted by the supposed “emergency” status.

Layered over all of this is the emergence of the new SARS-CoV-2 variant, omicron, that is providing authorities in Europe and North America further justification to mandate or coerce people to be jabbed, most notably with so-called “boosters” (presently existing stock of injections based on the original Wuhan strain, Wuhan_Hu-1).

Much hype is being generated by emerging evidence of omicron’s superior transmissibility compared with delta.

Policies designed to increase “vaccination” coverage and re-injection of previously injected people (use of “boosters”) are not based on any conclusive data or even mechanistic evidence on the likely effectiveness of this strategy.

Instead, they rely on now outdated data from Israel and England that an mRNA booster jab can reduce the chances of people getting severely ill if infected.

Such data are entirely irrelevant to a situation we might be in in the coming weeks if omicron becomes dominant. That’s because it is increasingly clear that the vaccinal antibodies elevated by the jab do precious little to protect people, given that omicron’s multiple mutations in the receptor-binding domain of its spike protein prevent the antibodies from neutralizing it.

With all the coercion around us it is more important than ever that people really understand what the jabs are and how they work. We now know a little more about them compared with when they were first released on the public, so let’s have a closer look.

We will restrict our discussion to the two main types of “vaccines,” the mRNA and non-replicating viral vector types, respectively, that include 5 of the 8 World Health Organization-approved COVID-19 injections (Table 1).

Table 1. WHO approved COVID-19 injections

ANH WHO approved Covid-19 injections Table 1
Source data: COVID-19 Vaccine Tracker

Why the COVID-19 jabs shouldn’t be described as ‘vaccines’

In a recent video I explained why the main contenders (mRNA and viral vector types) should not be described as “vaccines” as they don’t meet the World Health Organization’s definition of being the administration of “agent-specific, but safe, antigenic components that in vaccinated individuals can induce protective immunity against the corresponding infectious agent.”

That’s because both these jab types don’t actually contain any antigenic components.

They contain genetic information that forces the body of the vaccinee to make antigenic components, namely the spike protein of the now no-longer-circulating Wuhan strain of SARS-CoV-2.

This is succinctly put by two eminent Austrian vaccine scientists from the Medical University of Vienna, Franz Heinz and Karin Stiasny, in their detailed review paper in a Nature journal, NPJ Vaccines, where they state that both types of “vaccine” “… do not contain the spike protein but provide genetic information for its biosynthesis in body cells of the vaccine.”

The U.S. Centers for Disease Control and Prevention (CDC) chose to revise its definition of a vaccine on Sept. 1 so the mRNA and viral vector jabs wouldn’t fall foul of it.

The vaccine definition changed from, “A product that stimulates a person’s immune system to produce immunity to a specific disease, protecting the person from that disease,” to the broader, more inclusive definition, “A preparation that is used to stimulate the body’s immune response against diseases.”

Other health authorities will undoubtedly follow suit as these new platforms become more and more widely used, and not just to target this one pathogen.

Such is the “let’s make it up as we go along” approach, we noticed, at the time of writing, the CDC has failed to update the “vaccine” entry on this glossary.

In their comprehensive review, Heinz and Stiasny refer to both the mRNA and viral vector type products as “genetic vaccines” — because they deliver genetic information to the body to make it synthesize the antigen. This is why the term “gene therapy products,” while having been branded repeatedly as conspiracy theory, is a reasonable description.

A paper published in the journal Genes and Immunity states that COVID-19 “vaccines” “… signify a breakthrough in the field of gene therapy, which has battled to achieve ordinary acknowledgement [sic] due to a large number of sceptical [sic] and conservative scientists and other claimed safety and translational concerns.”

The “vaccine” tag could be viewed as particularly misleading given the products are not capable of generating herd immunity as they don’t elicit a strong enough sterilizing response from antibodies to prevent infection and transmission.

Furthermore, and contrary to what is inferred by health authorities, comprehensive research using a pseudovirus that expressed spike protein in Syrian hamsters conducted at the Salk Institute found that the spike protein (Fig 1) was far from harmless.

It appears to be toxic in its own right and it is the primary component that induces the vascular disease that develops in severe, life-threatening cases of COVID-19.

The spike protein of SARS-CoV-2

 

Figure 1. The spike protein of SARS-CoV-2, coated in sugar molecules (glycans), with receptor-binding domain in the upper, S1 subunit. Source: Nature, 2021

What might be in the vials that isn’t declared?

The simple answer is we don’t know. We know what we’re being told is in them, but there is increasing evidence of big variations in the quality and composition of different batches, which may or may not be deliberate.

Contaminants, described in mainstream media articles as “black particles,” have been found in Japan as having “white floating matter” in the Pfizer jabs.

There has also been considerable speculation around the presence of other materials that do not appear on the official datasheets, notably reduced graphene oxide (rGO), in the injection products. Graphene is a single atom thick layer of bonded carbon atoms arranged in a hexagonal pattern.

It has many remarkable properties and has been extensively researched for its ability as a potential vaccine carrier and adjuvant.

Dr. Pablo Campra from Almeria University in Spain published a report on Nov. 2 claiming the detection of graphene in the Pfizer “vaccine.” An English translation can be found here and a video and more information here.

One group of anonymous scientists that appear to be based in Germany also reported at a conference finding graphene oxide in samples of all 5 of the WHO-approved “vaccines” considered here. Video material from the conference is readily accessible here.

More information and videos can be found on NotOnTheBeeb.

Contesting these highly controversial views are fact-checkers and mainstream news channels galore, as one would expect, but no serious analytical chemists.

Other than potential contaminants or hidden ingredients, there is also the possibility of being injected with nothing other than saline.

What should be in the vials?

Let’s now look at what should be in the two types of “genetic vaccines,” summarized in Table 2.

Table 2. Claimed key ingredients in the 5 main WHO-approved COVID-19 injections

ANH Claimed key ingredients WHO approved Covid-19 injections

*Pfizer/BioNTech (Cominarty) contains:
4-hydroxybutyl)azanediyl) bis(hexane-6,1-diyl) bis(2-hexyldecanoate, (ALC-0315), 2-[(polyethylene glycol)-2000]-N,N-ditetradecylacetamide (ALC-0159), 1,2-Distearoyl-sn-glycero-3-phosphocholine (DSPC)
Moderna (Spikevax) contains: Lipid SM-102 (heptadecan-9-yl 8-{(2-hydroxyethyl)[6-oxo-6-(undecyloxy)hexyl]amino}octanoate), 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC), 1,2-Dimyristoyl-rac-glycero-3-methoxypolyethylene glycol-2000 (PEG2000 DMG), Trometamol, Trometamol hydrochloride

mRNA type

Both the Pfizer and Moderna jabs rely on similar technologies, namely mRNA (messenger RNA) that is a transient intermediary between genes and proteins. Companies like Moderna have been founded to exploit the potential to use this technology to get the body to produce an array of therapeutic proteins.

The Moderna jab relies on over three times as much mRNA as that of Pfizer. The messenger RNA (mRNA) is synthetic and now commoditized, encoding instructions that force the vaccinee’s cellular machinery to produce a modified form of the full-length SARS-CoV-2 protein.

Configuration of mRNA vaccines

 

Source: Heinz FX, Stiasny K. npj Vaccines. 6, 104 (2021)

The RNA sequence in each of the two mRNA “vaccines” is modified from the one used by the actual SARS-CoV-2 virus when it co-opts particular organelles in cells (endoplasmic reticulum and ribosomes) to translate the RNA that is converted to DNA to make its own spike proteins.

The uridine bases are all substituted for N1-methylpseudouridine to make the mRNA both evade the immune system and enhance protein production. The RNA strand is also “capped” and “tailed” with methylguanosine and poly-adenine, respectively, to further stabilize the mRNA and promote its translation.

The genetic instructions have yet another trick in store that’s at odds with what happens when hosts produce spike proteins from the RNA of beta-coronaviruses.

Two mutations that involve proline substitutions are built in at the beginning of the central helix of the spike protein to force it to stay in its “up” prefusion conformation — the state it’s in before it enters cells, after which it switches to the “down” position.

This unnatural “up” position forced upon it by the structurally stiff proline molecules is intended to increase the exposure of the spike protein to the host’s immune system. This way it increases the amount of neutralizing antibodies generated through the humoral (adaptive) immune response.

Each mRNA sequence is encased in a nanoparticle comprised of three main components: an ionizable phospholipid (phosphocholine), a sterol and a lipid-anchored polyethylene-glycol (PEG) molecule.

This is in effect a targeted drug delivery system that’s never been used at scale before — certainly not in efforts to treat a global population. The lipid nanoparticle (LNP) is multi-functional in that it protects the very fragile mRNA, reduces particle aggregation and exploits the tendency of cell membranes to draw the lipid (along with its mRNA cargo) into cells.

It is too early to fully understand how new-to-nature mRNA, modified spike proteins and lipid nanoparticles will affect those injected in the long term.

The likelihood is that these synthetic genetic “vaccines” that are injected directly into our bodies present a substantially greater risk to our species than the consumption of genetically modified foods that have been the subject of open scientific and public discourse for decades, with millions of consumers choosing to avoid their consumption.

Furthermore, it is now well known that the LNPs do not remain in the deltoid muscle injection sites, a fact that was revealed on disclosure of a Japanese biodistribution study used by regulators to grant Emergency Use Authorisation of the Pfizer jab.

The possibility of the mRNA being delivered to a young woman’s ovaries is more than a possibility. If it were to encode for the spike protein, toxicity or an immune response it could adversely affect fertility.

It is our view that there is no conclusive evidence that these “genetic vaccines” will not adversely affect fertility of either women or men. This risk is likely to increase with successive exposure to the jabs.

Viral vector type

While these “genetic vaccines” also get the body to produce the spike protein, they are more complex in nature. Unlike RNA jabs that are entirely synthetic in origin, they rely on mammalian cell cultures.

The adenoviral vectors are derived from chimpanzees and are subject to two key mutations: one that eliminates the E1 gene that stops the virus from replicating once in a vaccinee, the other that inserts the DNA of the adenovirus, a cloned gene that encodes for the full-length spike protein.

Viral vector type
Source: Heinz FX, Stiasny K. npj Vaccines. 6, 104 (2021)

In the Oxford-AstraZeneca, Gamaleya and CanSino “vaccines,” viral vector particles are sourced from primary human fetal kidney cells (HEK293). The Janssen “vaccine” relies on human fetal retinal cells (PER.C6) (Table 2).

The process is complex and involves detergents and filters to remove free viral DNA and other debris. On all accounts, some 80% of the overall protein content of the jab may in fact be impurities from the fetal cell lines. Heinz and Stiasny separately calculated that the total protein content of the 50 billion adenoviral vector particles would amount to about 8 micrograms.

Yet a separate study found that the actual protein content was much higher, at between 35 to 40 micrograms. This additional amount (80%) must be related to protein-rich cellular impurities from the human fetal cells lines.

Have religious groups, vegetarians and vegans been informed of the presence of this human cell line debris?

Instead of the spike protein being made in the cytoplasm and endoplasmic reticulum outside the nucleus of the cell, the viral vectors rely on the adenoviral DNA entering the nucleus and transcribing itself to RNA before it can generate the spike protein.

The additional steps mean there are greater possibilities for aberrant genetic processes and transcription patterns, as shown by Almuqrin and colleagues. Animal experiments have shown that the adenoviral DNA, in contrast to mRNA, may remain viable and detectable for months following injection, this being one reason that viral vector jabs are less prone to waning immunity.

Do the ‘vaccines’ contain nanotechnology?

The LNPs in the Pfizer and Moderna jabs certainly are sub-100 nanometers in size. The adenoviral vector types rely on chimp adenoviruses that are typically at or just above this relatively arbitrary threshold.

However, given that size really does matter when it comes to changes in biological properties, the lack of robust safety data on the LNP-dependent mRNA jabs is of particular concern.

Equally concerning is that the public keeps being told there’s no nanotechnology in the jabs. Take a quote by Mark Lynas, a visiting fellow at the Alliance for Science and Cornell University, for example. He said, “None of the vaccines contain nanotechnology of any sort, let alone ‘transhumanism nanotechnology,’ which isn’t even a thing.”

Unfortunately, Mark Lynas, who writes for the New York Times, the Washington Post, the Wall Street Journal, the Guardian and CNN.com, is wrong on both counts. As we’ve already seen, the LNPs in the Pfizer and Moderna jabs are most certainly nanoparticles given their size distribution. The game is given away even in their name (LNPs)!

Then there’s the transhumanism claim. It is a thing — potentially a very real thing in the eyes of those who are pushing jabs as the only way out of this “pandemic.” For an introduction to transhumanism, you might want to dive into a somewhat conventional take on the subject via Wikipedia.

You might also want to check out the Fourth Industrial Revolution (Penguin, 2017), by founder of the World Economic Forum, Klaus Schwab. He describes this as a revolution “characterized by a fusion of technologies that is blurring the lines between the physical, digital, and biological spheres.”

Mark Lynas seems unaware of the insights of Schwab and other transhuman proponents on designer beings or humans with gene-edited artificial memories.

To create a robust and durable immune response, you ideally need trained innate immunity coupled with well-integrated adaptive immunity made up of an appropriate humoral (B cell-derived neutralizing antibodies) and cell-mediated (CD4+ and CD8+ T cells) response.

Spike protein-focused COVID-19 jabs largely elevate neutralizing antibodies that only partially neutralize the spike protein of the delta variant (even less so for omicron), while damaging both the innate immune and cell-mediated (T cell-based) adaptive immune response.

It’s a pandemic of the unvaccinated, right?

The UK Health Security Agency (UK HSA), formerly Public Health England, had a long-standing reputation, since the news of a new coronavirus in Wuhan broke in early 2020, as being one of the most comprehensive datasets for epidemiological study.

By October 2021 there was an emerging picture of catastrophic failure of the technology that so much of the industrialized world had appeared to pin its hopes on. That included data from the UK HSA.

It wasn’t long before one of many changes in reporting changed the pattern of the data. Initially, it was hard to understand why a process that had looked like increasing “vaccine” failure had suddenly turned itself around, with vaccinees appearing to have better outcomes in terms of cases, hospitalizations and deaths than the jab-free.

We started finding anomalies in the data on supposedly COVID-caused or all-cause mortality and immediately sensed that what might be going on was that the people who had been initially jabbed were being counted as jab-free.

Then we saw that Dr. Martin Neil and Prof. Norman Fenton of Queen Mary, University of London, along with a number of other colleagues, had done a stunning analysis of the latest UK HSA data.

Don’t expect a major journal to have published the work — as these have all been systematically blocking publication of any scientific views or analysis that contradicts the mainstream narrative. So you’ll have to read the paper, for now at least, on the preprint server Researchgate.

What the researchers found once they’d adjusted all-cause mortalities for likely miscategorizations of deaths was that the jabs had no benefits whatsoever. The first signal that something was wrong came when they saw consistent spikes in all-cause mortality deaths of specific age groups of the jab-free.

These coincided with the exact times that jabs were being rolled out to these age groups! How could the jab-free be affected? The answer appears to be: when the reportedly jab-free are actually the jabbed.

Their work is truly disturbing and concludes not only that there was almost certain systemic miscategorization of deaths between the different categories of unvaccinated and vaccinated, but also delayed or non-reporting of vaccinations, systemic underestimation of the proportion of unvaccinated, and/or incorrect population selection for COVID deaths.

It remains to be seen how the UK HSA will respond — but chances are the publication will either be ignored because it was not published in a peer-reviewed journal or Neil and Fenton will become targets for abuse and ridicule.

One thing is for sure: the UK HSA can no longer be trusted for its data quality.

Some numbers:

  • Over 5.8 million genome sequences of SARS-CoV-2 have been shared with GISAID.
  • 55% of the world population has received at least one dose of a COVID-19 jab.
  • 21 billion doses have been administered globally.
  • 87 million are estimated to be administered every day.
  • Only 6.2% of people in low-income countries have received at least one dose.
  • Only 7.7% of people in the African continent have received at least one jab.

Source: Our World In Data 

COVID-19 jab coverage by continent.

 

Figure 1. COVID-19 jab coverage by continent.
People vaccinated by country chart
Figure 2. COVID jab coverage in selected countries as of 6 December 2021.

Omicron update

Last week, we published a detailed article on the omicron variant that provided evidence suggesting that it was improbable that the variant originated in southern Africa. We figured it was politically expedient for Africa to be placed under huge pressure to increase its vaccination coverage (see Figs 1 and 2).

Will omicron successfully outcompete delta worldwide? Emerging data from the Tshwane District in South Africa, which has been described as the “global epicentre of Omicron Outbreak,” suggest omicron has been able to outcompete delta in this area and it appears likely this trend will be seen elsewhere.

Final word

This article scrapes the surface of what is known and not known about these gene therapy products widely misrepresented as “vaccines.” More than that, misrepresented as “safe and effective vaccines.”

Omicron will be used as a lever to jab more people. Recognizing that the “ardently jab-free” constitute many of the remaining so-called hesitants, countries like Austria, Germany, Canada and Australia are resorting to mandates or extreme coercion.

European Commission president Ursula von der Leyen has seized the opportunity afforded by omicron to get EU countries to debate and consider mandatory “vaccination” given her concerns over “low vaccination rates” in Europe.

The very least anyone should expect in the face of a virus that is now on par for lethality to circulating flu is the right to informed consent. That means informing each potential vaccinee what’s in the jabs, what’s known and not known about the greatest experiment ever conducted by, and on, humanity, and what other options there are that are known to effectively combat infection by SARS-CoV-2.

In short, that would mean that nothing you’ve read in this article should come as a surprise to anyone who has been jabbed. And we know from our many discussions, lectures, webinars and conversations around the world over these last 12 or so months, we are a million miles from achieving the required level of understanding for informed medical consent to have been offered.

To help improve the potential for properly informed consent, while allowing others to exercise their right of refusal in those countries that have yet to introduce mandates, please share this article as widely as you can. Thank you.

Originally published by Alliance for Natural Health International.

© [12/9/21] Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

__________________

Please see:  https://madisonarealymesupportgroup.com/2021/12/01/death-by-1000-cuts-graphene-hydroxide-in-covid-shots/  Well-known German chemist and one of the EU’s top graphene experts, Dr Andreas Noack died suddenly just hours after publishing this latest video about graphene oxide and graphene hydroxide.  Graphene hydroxide molecules in the vaxx behave like nano razors that cut the epithelial lining of recipients’ veins, which he believes is the cause of blood clots and the sudden deaths observed in so many top athletes, lately.  (See link for more)

https://healthimpactnews.com/2021/realnotrare-new-website-for-covid-19-vaccine-injured/  Trailer Here

#RealNotRare New Website for COVID-19 Vaccine Injured

by Brian Shilhavy
Editor, Health Impact News

Dec. 9, 2021

A new website has been launched where people can tell their stories about being injured by one of the COVID-19 shots.

The name of the website is Real Not Rare, and they also have groups people can join, and it appears there is one group in each state.

They also have a “Take Action” section. Health Impact News subscribers will recognize quite a few of the people in their videos, as we have covered many of their stories here. (See link for article)

Watch their trailer in link above.

For more:  https://madisonarealymesupportgroup.com/2020/12/21/warning-3150-injuries-in-1st-week-of-covid-vaccines-among-american-healthcare-workers-pregnant-women-included/

Senator Johnson’s Correction of MSM & Senate Passes Resolution to Nullify “Vaccine” Mandate

http://  Approx. 30 min

‘He Wants To Deny The Reality Of What He Said, What He Did!’: Ron Johnson Rips Fauci On Senate Floor

Dec 8, 2021
Senator Johnson has to correct mainstream media’s smear campaign on what he said and what he didn’t say.  The spin-doctors are working hard to keep the spin going.
According to Robert F. Kennedy Jr., Fauci’s first instinct as national AIDS czar was to stoke contagion terror.  Further, a fearmongering 1983 article in the Journal of the American Medical Association warned that AIDS could spread by casual contact, when it was almost exclusive to IV drug users and homosexuals.  The world’s leading expert was “astounded” at Fauci’s “stupidity” as his statements did not reflect scientific knowledge.
A year later, Fauci had to acknowledge that health officials had never detected a case of the disease spread through “casual contact.”

The truth never stood in the way of a good money-maker, and Fauci’s been at it ever since – fearmongering, controlling, and claiming to embody science itself.

The Wall Street Journal won a Pulitzer Prize for its investigation of a deliberate HHS scheme to misrepresent AIDS as a general pandemic to secure greater public funding and financial support.
Sound familiar?
http://  Less than 1 Min

JUST IN: Senate Passes Resolution To Nullify President Biden’s Vaccine Mandate

Dec. 8, 2021

Wednesday evening, the Senate passed a resolution to nullify President Biden’s vaccine mandate, as Sens. Joe Manchin (D-W.Va.) and Jon Tester (D-Mont.) voted with their Republican colleagues against Biden’s measure.  The vote came one day after a U.S. District Judge for the Southern District of Georgia, issued a 28-page ruling suspending the mandate nationwide.

At the press conference, Sen. John Hoeven (R-N.D.), who sponsored the CRA said:

“We’re gonna pass this Congressional Review Act on a bipartisan basis in the Senate sending a very clear message, a very clear message, that this is an overreach by the Biden administration and we need to stop it. And I think in the House, there’s a very good chance that they will get enough people to sign on to this CRA to actually force a vote.

“Now, we understand that when that goes to the administration the president may well veto it, but we’ve sent a very clear bipartisan message on behalf of the people that this mandate needs to be stopped.”

Go here for a good explanation.

http://  Approx. 10 Min

Biden’s Vax Mandate BLOCKED In The Senate, Pfizer CEO Says FOURTH Booster May Be Needed Amid Omicron

Dec. 9, 2021

Ryan Grim and Emily Jashinsky discuss Republican’s invocation of the Congressional Review Act to halt President Biden’s federal “vaccine” mandate.

FDA Panel Just Barely Recommends Molnipiravir. Data Show Birth Defects in Rats

https://popularrationalism.substack.com/p/fda-panel-just-barely-recommends

FDA Panel Just Barely Recommends Molnupiravir. Data Show Birth Defects in Rats

Health advisors vote 13 for and 10 against Molnupirivir for COVID-19 Patients. Issues with lack of evidence of efficacy against new variants and birth defects cause doubt.

The FDA may or may not take the weak recommendation by a health advisory committee. With 43% of the health advisors voting against recommendation, and the data on Molnupiravir lacking, the US awaits the decision by FDA on its recommendation position on Merck’s alleged “wonder drug”.

I had written early on the extraordinary hypocrisy of Molnupiravir, given that the press had advanced a press-release (not a peer-reviewed study) on the efficacy and safety of the drug. Even now, the peer-reviewed literature only includes studies with less than 20 patients for first-in-human and dose variation study.

Merck had decided to do an “interim analysis” of an ongoing clinical trial, and yet compared to the very strong evidence in support of Ivermectin in the reduction of hospitalization and risk of death (See https://ivmmeta.com).

So what made the 10 health advisors skeptical?

For one, data from studies in pregnant rats showed birth defects.

From CBS News:

“Given the large potential population affected, the risk of widespread effects on potential birth defects has not been adequately studied,” said Dr. Sankar Swaminathan of the University of Utah School of Medicine, who voted against the drug.”

With another example of hypocrisy, one panelist said that if the FDA restricts the use of molnupiravir in pregnant women, they would be denying women choice.

I don’t think you can ethically tell a woman with COVID-19 that she can’t have the drug if she’s decided that’s what she needs,” said Cragan, a panel member and staffer with the Centers for Disease Control and Prevention. “I think the final decision has to come down to the individual woman and her provider.”

Read that again.

When FDA panelists start considering the level of evidence available for their favorites pharma partners, and start arguing for informed consent and health freedom when it comes to vaccines, we can start taking them seriously.

Until then, they are just going through the motions and abusing the public trust and they, and the FDA’s decisions, do not deserve our respect or attention.

_________________

**Comment**

And yet, that same woman, or man, or even a medical doctor can not “decide” that they need ivermectin or HCQ because, well – that’s just bad and regulatory groups will pounce upon you.  Hypocrisy indeed.

Read this article on a comparison between Molnupiravir and ivermectin.

  • The cost of a complete five-day course of Molnupiravir is $700 — or $70 per pill. That amounts to a 4,000% markup over what it costs Merck to make the drug.
  • Citing 2013 prices provided by the WHO, Campbell said a five-day course of ivermectin — 10 3mg pills — costs $0.53. (However, at today’s U.S. prices, 10 3mg pills cost about $39).

India and Argentina no longer fear COVID, they simply treat it.  Sub-Saharan Africa is void of COVID due to widespread river blindness which was brought under control by insecticides and by large-scale distribution of ivermectin since 1989.

But, the only drug offered U.S. patients is the expensive, worthless drug remdesivir which caused more than 500 deaths in the first year of usage.  There have been 20 deaths in 19 years of ivermectin usage.  Source

  • The FDA, spurred by “multiple” reports of ivermectin ‘poisoning,’ lied when it put out a post on it causing “serious harm, seizures, coma, and even death”. When the author inquired on how many is “multiple,” she was told FOUR.  Yet, the FDA had no trouble approving remdesivir which has caused far more deaths.
But now, they are offering another expensive, worthless drug.