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11th of September, 2023, the U.S. Meals and Drug Management introduced¹ it had licensed reformulated monovalent COVID pictures via Pfizer and Moderna to be used in folks 12 years of age and older. Additionally they issued emergency use authorization (EUA) to be used of the reformulated jabs in kids elderly 6 months to 11 years.²

The up to date mRNA injections include a unmarried changed RNA mentioned to correspond to the Omicron variant XBB.1.5., which used to be the dominant variant within the U.S. for many of 2023, however which has since been changed via different variants.

Consistent with government, alternatively, this pressure is other sufficient from the traces in any of the former pictures to suggest everybody take it, irrespective of your earlier COVID jab historical past.³

Thankfully, maximum American citizens don’t seem to be falling for a similar lies this time round. Maximum have discovered that the pictures are useless and will motive all forms of well being issues, together with coronary heart harm and immune gadget deregulation. The general public also are bored with the endless boosters.

In all, high-risk folks (such because the aged and/or immunocompromised of every age) who had been beneficial to get further doses may have won as many as six mRNA injections at this level — a three-dose number one collection in 2021,⁴ two boosters to the main collection right through 2021/2022,⁵ and one bivalent booster within the fall of 2022.⁶ The newest reformulation for XBB.1.5 would be the 7th in simply 3 years.⁷

Non-mRNA Shot Licensed as Public Rejects mRNA

Uptake of the brand new monovalent pictures has been disappointing, alternatively. As of October 12, 2023, handiest 7 million American citizens had rolled up their sleeves. For comparability, via October 12, 2022, greater than 18 million had won the bivalent booster launched that September, and via Would possibly 2023, 17% of the inhabitants — 56.5 million other people — had won it.⁸

Assuming the U.S. inhabitants is 340.47 million other people,⁹ 7 million is handiest about 2.06%. Consistent with CIDRAP Information,¹⁰ booster uptake is being “hindered via prior infections” and “concern of unwanted side effects.” That’s what an October 2023 learn about¹¹ discovered. As famous in that paper:

“Essentially the most often reported reason why for no longer having been boosted used to be a previous SARS-CoV-2 an infection (39.5%), adopted via fear about vaccine unwanted side effects (31.5%), believing that the booster would no longer supply further coverage over the vaccines already won (28.6%), and fear about booster protection (23.4%) or that it will no longer give protection to from SARS-CoV-2 an infection (23.1%).

For topics associated with causes for no longer having been boosted, the ones 60 years of age or older had been much less most probably to make a choice pieces associated with wisdom or logistical issues in regards to the vaccine; whilst the ones reporting Hispanic ethnicity had been much more likely to put across issues about logistics than the ones reporting non-Hispanic ethnicity.

In any case, in comparison to school graduates, the ones with some school or technical college had been considerably much more likely to make a choice pieces associated with the dangers and advantages of the bivalent vaccine no longer being transparent as causes for no longer having been boosted.”

Notice how they downplayed other people’s fear about vaccine unwanted side effects. They separated “fear about vaccine unwanted side effects” (31.5%) and “fear about booster protection” (23.4%), which is the very same factor. Upload them in combination, and 54.9% are skipping additional boosters because of fears about their protection.

To Allay Fears, FDA Grants EUA to Non-mRNA COVID Vaccine

The FDA’s authorization¹² of an up to date non-mRNA COVID vaccine — Nuvaxovid, a subunit protein vaccine made via Novavax — is reportedly a part of the way to inspire uptake amongst those that are “hesitant in regards to the mRNA vaccines.”¹³

The up to date Novavax vaccine used to be approved via the FDA in early October 2023 for ages 12 and older, irrespective of earlier COVID jab standing. Like Pfizer’s and Moderna’s new pictures, the up to date Nuvaxovid goals the SARS-CoV-2 variant XBB.1.5, and the FDA is encouraging other people to make a choice whichever shot they like (mRNA or non-mRNA).¹⁴

Novavax Is No longer The use of Smartly-Examined Generation Both

Whilst Novavax isn’t the use of the mRNA platform, it’s no longer the use of solely attempted and true vaccine generation both. Somewhat than rising the viral protein in eggs or mammalian cells, as has been performed for many years, the corporate is generating the SARS-CoV-2 spike protein in moth cells.¹⁵ As defined via NebraskaMed.com:¹⁶

“The Novavax manner makes use of moth cells to make spike proteins:

‘The Novavax vaccine has no genetic subject material, handiest proteins,’ says Dr. Florescu. ‘The vaccine generation is extra conventional, and it is similar to a protein-based influenza vaccine.’”

Nuvaxovid additionally incorporates a proprietary adjuvant known as Matrix-M, which is in accordance with saponin extracted from the bark of the Chilean soapbark tree. Like different adjuvants, it boosts your frame’s immune response to the viral protein, which permits a smaller dose of spike protein for use. Consistent with revealed research, Matrix-M has a very good protection profile, however the place have we heard that earlier than? I, for one, will look forward to impartial corroboration earlier than making such claims.

Effectiveness and Protection of Novavax

Novavax is alleged to have the similar level of effectiveness as the opposite COVID pictures. Consistent with a learn about¹⁷ revealed in early October 2023, the Novavax vaccine launched in overdue 2021 used to be 31% efficient in opposition to identified SARS-CoV-2 an infection and 50% efficient in opposition to symptomatic COVID-19 right through the primary 4 months. Just like the mRNA pictures, effectiveness in opposition to an infection waned from there.

As for protection, Novavax seems to be much less dangerous than the mRNA pictures in relation to myocarditis and different heart-related harm, however severe unwanted side effects do happen, as evidenced in information¹⁸ from the Facilities for Illness Regulate and Prevention.

Out of a cohort of one,148 teenagers elderly 12 to 17, 52 (3.6%) skilled a serious systemic match after the primary dose of Novavax, and 304 (21.9%) had a serious systemic match after the second one dose. One teenager boy used to be identified with myocarditis after his 2d dose, and the FDA formally concluded that his situation used to be “associated with the vaccine.”¹⁹

Amongst adults, ages 18 to 64, 2.4% skilled a significant systemic antagonistic match after the primary dose and 13% had a significant match after the second one dose. A few of the aged (65 and older), 1.6% had a significant match after the primary dose and four.4% after the second one.²⁰ So, obviously, Novavax seems to be some distance riskier for more youthful other people than older ones.

Interestingly, on the closing minute, the Ecu Medications Company (EMA) made up our minds to chase away its authorization of the up to date Novavax shot, and is calling the corporate for additional info. In August 2022, the EMA beneficial Novavax upload a caution about the potential of coronary heart irritation to its vaccine.²¹

So, what’s the EMA desirous about now that the FDA isn’t? “FDA did authorize it — however don’t take it, as there should be a vital drawback,” Dr. Meryl Nass warned in an October 16, 2023, Substack submit.²²

The place’s the Emergency?

As discussed, the FDA has handiest approved Novavax for emergency use. It does no longer have complete approval. However wait a 2d. Wasn’t the COVID emergency declaration formally ended Would possibly 11, 2023? It positive used to be, so, how can the FDA factor Emergency Use Authorization (EUA) for Novavax when there’s no emergency?

Brief resolution: the FDA made up new laws at the fly. Once more. As famous within the FDA’s letter to Novavax, dated October 3, 2023:²³

“On February 4, 2020, as amended on March 15, 2023, pursuant to Segment 564(b)(1)(C) of the Federal Meals, Drug, and Beauty Act … the Secretary of the Division of Well being and Human Services and products (HHS) made up our minds that there’s a public well being emergency, or a important possible for a public well being emergency, that has effects on, or has a vital possible to impact nationwide safety or the well being and safety of United States voters dwelling in a foreign country, and that comes to the virus that reasons Coronavirus Illness 2019 (COVID-19) …

On July 13, 2022, the Meals and Drug Management (FDA or the Company) issued an Emergency Use Authorization (EUA) for emergency use of the Novavax COVID-19 Vaccine … pursuant to Segment 564 of the Act … On October 3, 2023, having concluded that revising this EUA is acceptable to offer protection to the general public well being or protection below phase 564(g)(2) of the Act, FDA is reissuing the Would possibly 11, 2023 letter of authorization …”

The emphasis within the above paragraph is mine. There are a number of curious issues happening right here. For starters, in keeping with this letter, the FDA approved Novavax in accordance with the POTENTIAL for a public well being emergency, no longer a real emergency.

Secondly, it specifies that this possible public well being emergency should impact both nationwide safety or the well being of American citizens “dwelling in a foreign country.” Isn’t that curious? Why is there no point out of U.S. voters who reside in the US? To reiterate, the prospective emergency handiest covers two issues: threats to nationwide safety and voters who reside in a foreign country.

In studying the modification within the Federal Sign in,²⁴ the cause of this oddity turns into transparent. That’s the one justification the secretary may just use to claim an “imaginable emergency” that might authorize the FDA to factor the EUA.

There are handiest 4 eventualities below which the HHS secretary can justify EUA and the opposite 3 require us to be below assault from a chemical, organic, radiological or nuclear weapon.

The HHS isn’t going to confess SARS-CoV-2 is a bioweapon, so the HHS Secretary selected the one justification to be had, which is a “possible” public well being emergency “that has effects on, or has a vital possible to impact, nationwide safety or the well being and safety of United States voters dwelling in a foreign country.”

That choice approved the FDA to factor an EUA to Novavax although no emergency exists, and although American citizens dwelling within the U.S. don’t seem to be even lined via the prospective emergency. It’s ridiculous, however that’s the place we’re.

mRNA-Similar Deaths Is the Actual Emergency

If there’s an emergency, it’s that youngsters and younger adults are death in file numbers and individuals are linking the ones deaths to the mRNA pictures, therefore the dramatic drop in booster uptake.

As reported via Dr. William Makis²⁵ and the Moral Skeptic,²⁶ the surplus mortality for beginning to 24-year-olds is now at 41.7% — an ancient excessive, and hugely upper than 2020, when extra mortality for this age workforce remained neatly inside ancient norms.

They Used COVID to Get Untested Vaccines to Marketplace

Importantly, similar to the up to date mRNA pictures, the up to date Novavax vaccine has no longer passed through further checking out. It’s protection is solely in accordance with the unique method, investigational monovalent and bivalent vaccines that didn’t make it to marketplace, and postmarketing information.

Consistent with the FDA,²⁷ “The knowledge collected … are related to Novavax COVID-19 Vaccine, Adjuvanted (2023-2024 Method) because the vaccines are manufactured the use of a identical procedure.” Then again, it’s no longer the producing procedure by myself that determines how dangerous an mRNA shot could be. The antigen used, and different components that can or would possibly not have modified, most probably play a much more necessary position.

Bearing in mind the spike is probably the most pathogenic a part of the virus, and the reformulated pictures include a wholly other spike, how are we able to think that the protection shall be similar to that of the unique pictures that had been in accordance with the Wuhan spike? We will’t.

What we’ve got now could be a brand spanking new paradigm the place vaccines are allowed to be delivered to marketplace with out checking out, which certainly is a vaccine maker’s dream come true. They’re additionally blatantly ignoring transparent EUA laws and misusing authority to claim emergency when none exists.

Additionally, recall the FDA authorized Comirnaty whilst concurrently extending EUA for the Pfizer-BioNTech jab. It used to be a vintage bait and turn, as other people had been informed to get the now “absolutely authorized” jab, when actually the pictures they won weren’t authorized in any respect, however nonetheless the experimental and unlicensed EUA product.

Consistent with the regulation, EUA can handiest be given when there’s no licensed selection, so as soon as Comirnaty used to be licensed, the FDA misplaced its criminal talent to keep ANY of the EUAs, despite the fact that there used to be a real emergency.

Well being Government Have Long past Rogue and Make Their Personal Regulations

Have been the regulation adopted, Comirnaty will be the handiest COVID jab to be had within the U.S., however right here we’re, with out a emergency and EUAs for each mRNA pictures (Pfizer’s and Moderna’s 2023 components for youngsters elderly 6 months to 11 years²⁸) and Novavax, for any person 12 and older.

On most sensible of that, EUA merchandise had been added to the youth vaccination time table, which is a transparent violation as neatly. The rationale in the back of it’s because that used to be the one option to completely indemnify Pfizer and Moderna from monetary legal responsibility for accidents and deaths.

Present EUA merchandise also are freed from legal responsibility, for the reason that Public Readiness and Emergency Preparedness (PREP) Act legal responsibility defend for the COVID-19 vaccines has been prolonged via Dec. 31, 2024,²⁹ although the emergency declaration resulted in Would possibly 2023.

Each and every choice made via the FDA and CDC to this point issues to the truth that they intend to get rid of clinical rigor and simply take a look at new vaccines and gene treatments without delay at the public. Proof additionally tells us they’ve no qualms in regards to the dying toll. At absolute best, they don’t care what number of people die. At worst, they hope to maximise extra deaths.

It’s onerous for the common particular person to know how well being government might be so callous, however when you remember the fact that those companies are operating with the similar globalist cabal this is pushing the golf green time table (the place people are to be displaced to offer protection to the surroundings), the transhumanist time table (which seeks to turn into mankind into organic robots) and the eugenics time table (which seeks to do away with “unnecessary eaters” and save you them from breeding), it turns into more uncomplicated to peer why mass dying could be an appropriate end result, if no longer a function in itself.

Were given the Jab? Take Motion to Safeguard Your Well being

Should you already were given a number of jabs and still have issues about your well being, at the start, by no means take some other COVID booster, some other mRNA gene treatment shot or common vaccine. You wish to have to finish the attack for your gadget.

Should you evolved signs you didn’t have earlier than your shot, I’d inspire you to hunt out knowledgeable assist. At the moment, the Entrance Line COVID-19 Crucial Care Alliance (FLCCC) turns out to have one of the vital absolute best remedy protocols for post-jab accidents. It’s known as I-RECOVER and may also be downloaded from covid19criticalcare.com.³⁰

Dr. Pierre Kory, who cofounded the FLCCC, has transitioned to treating the vaccine injured roughly completely. For more info, see DrPierreKory.com. Dr. Peter McCullough could also be investigating post-jab therapies, which you’ll to find on PeterMcCulloughMD.com.

The International Well being Council has additionally revealed lists of therapies that may assist inhibit, neutralize and do away with spike protein, which most mavens agree is the main perpetrator. I lined those in my 2021 article, “International Council for Well being Finds Spike Protein Detox.”

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