The Intelligence-Industrial Complex and their various partners-in-crime such as BigPharma, the MSM Mockingbird quislings, and the wholly captured academic peer-reviewed journals were activated to disseminate their disinformation campaigns and publish their fraudulent scientific papers; for example:

In other words, what we witnessed was mass deceit and crimes against humanity, because these NWO globopedo assets always knew that these lifesaving compounds not only cure all viral infections, but they also cure cancer, and not just the turbo cancer variety caused by these very Modified mRNA slow kill bioweapon “vaccines” that they were only able to push through because they falsely maligned Hydroxychloroquine and Ivermectin — and then their FDA coconspirators were ordered to approve the criminal “emergency” use authorization (EUA), which then kicked off the severe adverse events VAIDS epidemic we are now living through.

But there is much hope, and at the end of this article an important lifesaving protocol will be shared.

by David Gortler, Pharm. D

Early January of 2024, Americans learned about the publication of an article from Elsevier’s Journal of Biomedicine and Pharmacotherapy overseen by Dr. Danyelle Townsend, a professor at the University of South Carolina College of Pharmacy’s Department of Drug Discovery and Biomedical Sciences. As Editor-in-Chief, Dr. Townsend reviewed, approved, and published the article titled: “Deaths induced by compassionate use of hydroxychloroquine during the first COVID-19 wave: An estimate.”

The article was always a hypothesized estimate of people that might have died, but now even that estimate has been retracted. The reason for the retraction was that the Belgian dataset that was one of the bases for the piece was found to be “unreliable” (but in reality was fraudulent). The article also repeatedly referenced the New England Journal of Medicine’s 2020 RECOVERY trial. The RECOVERY trial is well known to be a deeply flawed study which, in addition to implementing late treatment in severely ill Covid patients, used extremely high doses of HCQ.

The now retracted publication authors were all French or Canadian, with the primary author a pharmacist by the name of Alexiane Pradelle. According to a rudimentary internet search, Dr. Pradelle had never published before. Subsequently, listed authors were degreed as physicians, pharmacists, and/or professors of their respective disciplines. The main, corresponding author, Jean-Christophe Lega, runs the Evaluation and Modeling of Therapeutic Effects team at the University of Lyon.

Hydroxychloroquine’s Fabled Safety History Contrasts Data

In addition to being a hypothesized estimate, the article also attacked the legendary safety of HCQ, contradicting centuries of the safety of quinolines as a class.

HCQ, chloroquine and quinine are structurally and pharmaceutically/mechanistically related, sharing the same quinoline structural group. The original iteration of quinine was a very fortunate discovery that dates back to the 1600s (at least) as a medicinal tipple used by Jesuit missionaries in South America. It is naturally found in the bark of the Cinchona tree (also called a “Quina-Quina” tree).

Quinine is still available today both as a prescription drug, for similar indications as HCQ including malaria…and as a Covid-19 treatment.

Quinine is so safe that it may be unique in that the FDA simultaneously permits its use without a prescription, as an ingredient in tonic waters.

HCQ is similarly safe when used appropriately and under medical supervision.

The CDC describes HCQ as “a relatively well tolerated medicine” and that “HCQ can be prescribed to adults and children of all ages. It can also be safely taken by pregnant women and nursing mothers” referring to its long-term use in chronic diseases.

Basic logic dictates that, if a drug is safe for long-term use, it would also be safe for short-term use, including (and especially) in Covid-19 early treatment/pre-exposure prophylaxis type indications.

These are pharmacology fundamentals that ought to be known by any pharmacist or physician – let alone to a professor serving as a Journal Editor-in-Chief at a taxpayer-funded state College of Pharmacy.

Did not even one person on her editorial board of over 50 “peer-reviewers” and staff ponder the celebrated and storied history of HCQ (and its predecessors) and how incongruent this study’s findings were before choosing to publish data denigrating HCQ safety?

The correct answer to that might actually be: “no”…

The publishing editorial board all seem to be laboratory bench (non-clinical) research scientists, per their biographies. Although the board does promote itself as meeting DEI requirements of being “gender diverse,” a more important question might be is if they have the appropriate credentials and experience to review and opine on clinically complex drug safety/epidemiology subject matters in the first place.

Is just anyone now allowed to opine on specialty clinical pharmacology drug safety matters?

In certain journals/news publications, the answer to that question seems to be: “yes”…

Those “17,000 Deaths” Never Occurred

Another point of confusion surrounded the interpretation and promotion of this little-known publication by the lay press.

To be exact: there were never “17,000 deaths;” it was always a hypothetical extrapolation of people that could have died, based on “unreliable” (eg, actually, fraudulent) databases on top of the previously mentioned, problematic late-stage RECOVERY-trial-type dosing and timing.

Still, Josh Cohen, a Forbes.com PhD senior healthcare columnist, used this publication to headline an absurdly biased op-ed against HCQ, stating that Trump’s HCQ proposal was “Linked To 17,000 Deaths.” Forbes’ Tufts, Harvard, and the University of Pennsylvania- trained “healthcare analyst” misrepresented or appeared to not understand the now-retracted study methodology or projections.

It went downhill from there. Mere hours following the publication, very similar, now objectively inaccurate, highly politicized, and seemingly coordinated attacks on HCQ and Trump were published by: The Hill, Politico, Frontline News, Scripps News, the Guardian, KFF Health News, News Nation, Newsweek, AOL.com, Yahoo News, and Daily Kos, in addition to a multitude of prominent regional, international, and US federal news outlets, many falsely estimating that 17,000 deaths had already taken place and that the (imaginary) victims’ blood was already on Donald Trump’s hands.

As of September 15, 2024, the above and other articles still show up very prominently (on the first page) of a Google search for “hydroxychloroquine deaths”…which never happened.

Here are some screenshots of headlines referencing non-existent deaths based on a now-retracted study:

Journal Editors Were Immediately Warned about Questionable Findings

Almost immediately following the January 2, 2024 publication, its critical flaws including basic miscalculations among many other deficiencies were brought to the attention of Dr. Townsend by Xavier Azalbert and non-profit BonSens.org attorneys starting on Jan 7, 2024. In fact, a total of 9 communications were sent by the above individuals, but none of them were ever shared as “Letters to The Editor” by Dr. Townsend in good faith to inform readers of specific potential shortcomings, as is otherwise commonly done.

Dr. Townsend seemed to forget that bad medical data and publications can do actual patient harm, and kept legitimate and important study criticisms to herself. Instead of taking responsibility and making a leadership decision, she passed the buck to a Committee on Publication Ethics, delaying the needed retraction.

It appallingly took 234 days (~7 months, from the January 2nd publication to August 26th) for Dr. Townsend’s Journal of Biomedicine and Pharmacotherapy to finally retract the “unreliable” article. But at that point, untold millions around the world had already been (and continue to be) polluted with outrageously incorrect information about non-existent HCQ deaths.

This raises some questions about Dr. Townsend’s duties and responsibilities as the Editor in Chief:

• What efforts were made to correct incorrect headlines and articles published by the lay press, incorrectly frightening patients, pharmacists, and physicians, by fueling false tropes about HCQ?

• What efforts were made to let news organizations know that data from the peer-reviewed publication was under question? (She refers to “a number of Letters to the Editor and correspondence from readers.”)

• What immediate efforts are being made to notify news organizations and/or amplify search engine results regarding the now-retracted publication?

• What funding source/individual paid the $3,490 (“excluding taxes and fees”) publication fee? (Note: reputable academic journals do not charge to publish articles.)

• Does Elsevier’s Journal of Biomedicine and Pharmacotherapy meet certain definitions of what is known as a predatory publisher?

• Was this Editorial Board qualified to review regulatory/drug safety/epidemiology/any other clinical subjects?

• Are the ramifications of this Journal’s publication and its subsequent retraction known to the University of South Carolina administration, co-faculty, and whichever body adjudicates its faculty Code of Ethics & Standards of Practice?

• This isn’t the first time Townsend has needed to retract articles – a normally very rare occurrence for reputable journals. Will Elsevier, which publishes over 2,700 journals, permit further opining or publishing on clinical subjects by this editorial board? Can the Editor-in-Chief and/or editorial board be trusted to recuse themselves from opining on any topics that are not within their area of expertise?

• What should be done to prevent a reoccurrence of this incident at the University of South Carolina and other taxpayer-funded institutions?

Beyond that, what ramifications/punishments (if any) will occur for other prominent Covid-19 Lancet and New England Journal of Medicine authors/publishers whose articles were also retracted after they were found to be based on so-called “unreliable” (eg, non-existent) databases?

Ethical scientists who believe in truth, transparency, and academic accountability are standing by, waiting for medical and academic justice.

Unethical scientists are also watching this situation unfold, twisting their mustaches, learning about what they could potentially one day get away with.

DISCLAIMER: This article is not medical advice. Do NOT start or discontinue ANY drug without first discussing it with a pharmacist or physician you know and trust.

Is it any wonder then that just like Ivermectin always cured Covid-19 while also possessing potent anti-cancer properties…

…so too does Hydroxychloroquine…

…and if Orange Man Bad says a compound like Hydroxychloroquine may save lives — admitting that he was administering this truly safe and effective drug on himself as prophylaxis — then of course it must be anything but true…

…except that Trump and the real experts were all correct, but then Operation Warp Speed could never have been justified, and the deadly gene altering PSYOP-19 “vaccines” could have never been approved, and the crimes against humanity could have never been perpetrated on such a mass scale, and the mandates and “vaccine” passports could have never been instituted, and there would have never been the resultant turbo cancer epidemic to speak of.

Which brings us to the most comprehensive ‘holy grail’ cancer cure and prophylaxis in plain sight, that may also treat Alzheimer’s, mood disorders, Parkinson’s, Lyme Disease, Alpha-Gal Syndrom from Lone Star Disease, myocarditis, Hashimoto’s Disease, shingles (herpes), arthritis, Multiple Sclerosis, diabetes, asthma, leukemia, Lupus, skin conditions, various other “incurable” ailments, “vaccine” shedding, seasonal flu and even the common cold:

The Ultimate Disease Cure & Prophylaxis Protocol

• Tocotrienol and Tocopherol forms (all 8) of Vitamin E (400-800mg per day, 7 days a week). A product called Gamma E by Life Extension or Perfect E are both great.

• Bio-Available Curcumin (600mg per day, 2 pills per day 7 days a week). A product called Theracurmin HP by Integrative Therapeutics is bioavailable.

• Vitamin D (62.5 mcg [2500 IU] seven days a week).

• CBD oil (1-2 droppers full [equal to 167 to 334 mg per day] under the tongue, 7 days a week) CBD-X: The most potent full spectrum organic CBD oil, with 5,000 milligrams of activated cannabinoids and hemp compounds CBD, CBN & CBG per serving.

• Fenbendazole (450mg, 7 days a week) or in the case of severe turbo cancers up to 1 gram — for MEGADOSE 1,350mg-2,000mg/day — for prophylaxis one 150mg tablet once or twice per week

• Ivermectin (24mg, 7 days a week) or in the case of severe turbo cancers up to 1mg/kg/day — for MEGADOSE 120mg-200mg/day — for prophylaxis one 12mg tablet once or twice per week

• Hydroxychloroquine (10mg/kg/day 7 days a week) - for prophylaxis one 200mg tablet once or twice per week

• Doxycycline (100mg, 7 days a week for 30-60 days)

• ImmunX immune support which also greatly increases the bioavailability of both Fenbendazole and Hydroxychloroquine (2 capsules per day) — for prophylaxis 2 capsules per day

• Removing sugars and carbohydrates (cancer food) from your diet and replacing table sugar with a zero glycemic index, zero calorie, keto friendly rare sugar like AlluX

Do NOT comply.

⚡️The 50% OFF ChloroquineX Flash Sale⚡️ continues!

This is the biggest sale on this one product ever!

This sale only applies to ChloroquineX.

Please use code HCQ50 for 50% off on Hydroxychloroquine.

⚡️The 50% OFF ChloroquineX Flash Sale⚡️ ends Friday, September 18th (midnight eastern time), 2026.

Upon adding ChloroquineX to your cart, please go to the cart icon at the top right corner of your browser page and click it, then choose the VIEW CART option whereby you will be redirected to a page where you can enter the code HCQ50 in the Use Coupon Code field.

Only the RESOLVX HEALTH website offers all of the authentic products that this Substack promotes.

Please contact the company directly with any product questions: info@resolvx.health

Upgrade to paid

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…while the anti-cancer properties of Hydroxychloroquine were mentioned in passing, a pair of studies that Dr. Makis recently cited have inspired this Substack to revise the ‘New and Improved Joe Tippens Protocol’ at the end of this article such that we may now have an even more comprehensive cancer cure; to wit:

NEW ARTICLE: HYDROXYCHLOROQUINE and LUNG CANCER - Two studies show fascinating mechanisms of ANTI-CANCER action!

Papers Reviewed:
2019 Malhotra et al: “Phase Ib/II study of hydroxychloroquine in combination with chemotherapy in patients with metastatic non-small cell lung cancer (NSCLC)”

2018 Li et al: “Hydroxychloroquine induced lung cancer suppression by enhancing chemo-sensitization and promoting the transition of M2-TAMs to M1-like macrophages”

=====

The 2019 Malhotra paper talks about hydroxychloroquine as a cancer cell autophagy inhibitor to inhibit lung tumor progression:

“Preclinical studies in engineered mouse lung cancer models show that KRAS mutant lung tumors depend on autophagy, and inhibition of autophagy inhibits tumor development and progression.”

“autophagy inhibition appears achievable with hydroxychloroquine”

Results:
“The addition of hydroxychloroquine to chemotherapy was safe and resulted in modest improvement in response rate for select subgroup of patients with newly diagnosed metastatic NSCLC (KRAS-mutated tumors).”

“We also established that 200 mg BID of hydroxychloroquine in combination with chemotherapy is safe and tolerable”

=====

The 2018 Li paper discusses two important effects of Hydroxychloroquine on Lung Cancer:

1. HCQ enhances the sensitivity of lung cancer cells to chemotherapeutic drugs

HCQ functions as a chemo-sensitizer to enhance the anticancer effects of chemotherapeutic agents without killing cancer cells directly

HCQ reverses drug sequestration in lysosomes by increasing the lysosomal pH to inactivate P-gp

2. HCQ also exerts anti-tumor effect via immune microenvironment at tumor site

HCQ markedly decreased tumour weight in immunocompetent C57BL/6 J mice but did not show any influence in CD8+ T cell-depleted mice

HCQ induces CD8+ T cell-based tumour suppression via macrophages

HCQ induces the transition of M2-TAMs to M1-like macrophages

“results indicate that HCQ switches M2-TAMs into M1-like macrophages to enhance CD8+ T cell immunity”

“In summary, the data presented in this study clearly showed that by increasing the lysosomal pH in cancer cells and fostering the transition of M2-TAMs to M1 macrophages to induce CD8+ T cell anti-tumour effects, HCQ could function as a chemo-sensitizer and immune regulator to enhance the therapeutic effects of NSCLC.”

“HCQ is a promising agent for cancer treatment to improve the quality of life of NSCLC patients.”

It’s that interesting? 🤔

Maybe there was more to the attacks on HYDROXYCHLOROQUINE than just COVID-19 (!!)

Source

Just like there are high quality research studies showing that Ivermectin enhances the efficacy of chemotherapy, we now have irrefutable evidence that Hydroxychloroquine also greatly improves chemotherapy outcomes.

But these research studies never dare just have the repurposed drugs without the questionable chemotherapy as an other group, because then the Medical-Industrial Complexes most profitable “treatment” would be exposed for what it really is…

…and just like Ivermectin and Hydroxychloroquine are cures for all viruses, even the gain of function kinds, these compounds also not only treat the flu and the common cold, but a broad range of “incurable” diseases, which is why the likes of Dr. Fauci vehemently discredited them:

If Fauci had admitted that hydroxychloroquine or ivermectin were effective…it would’ve been illegal to use the ‘vaccines’…as the ‘vaccines’ made $200 BILLION DOLLARS…

,,,and just like the depopulation “vaccine” business rakes in well over $200 billion per year, so too does cancer “care” cost well in excess of $200 billion dollars per annum, with this egregiously high cost of cancer treatment in the U.S. not reducing mortality rates whatsoever.

If these repurposed compounds were used during the PSYOP-19 scamdemic, then not only would there have never been the fraudulent EUA approval by the wholly captured FDA, but global cancer rates would have plunged.

Instead, there is now a Modified mRNA slow kill bioweapon “vaccine” induced turbo cancer epidemic, which means that BigPharma’s and oncologist’s profits for cancer “care” will only exponentially increase going forward as more and more patients succumb to this extremely lucrative iatrogenesis.

Or why BigPharma does NOT want anyone ever finding out about this newly revised and further improved ‘holy grail’ cancer cure in plain sight, that may also treat Alzheimer’s, mood disorders, Parkinson’s, Lyme Disease, Alpha-Gal Syndrom from Lone Star Disease, myocarditis, Hashimoto’s Disease, shingles (herpes), arthritis, Multiple Sclerosis, diabetes, asthma, leukemia, Lupus, skin conditions, various other “incurable” ailments, “vaccine” shedding, seasonal flu and even the common cold:

The Ultimate Disease Cure & Prophylaxis Protocol

• Tocotrienol and Tocopherol forms (all 8) of Vitamin E (400-800mg per day, 7 days a week). A product called Gamma E by Life Extension or Perfect E are both great.

• Bio-Available Curcumin (600mg per day, 2 pills per day 7 days a week). A product called Theracurmin HP by Integrative Therapeutics is bioavailable.

• Vitamin D (62.5 mcg [2500 IU] seven days a week).

• CBD oil (1-2 droppers full [equal to 167 to 334 mg per day] under the tongue, 7 days a week) CBD-X: The most potent full spectrum organic CBD oil, with 5,000 milligrams of activated cannabinoids and hemp compounds CBD, CBN & CBG per serving.

• Fenbendazole (450mg, 7 days a week) or in the case of severe turbo cancers up to 1 gram — for MEGADOSE 1,350mg-2,000mg/day — for prophylaxis one 150mg tablet once or twice per week

• Ivermectin (24mg, 7 days a week) or in the case of severe turbo cancers up to 1mg/kg/day — for MEGADOSE 120mg-200mg/day — for prophylaxis one 12mg tablet once or twice per week

• Hydroxychloroquine (10mg/kg/day 7 days a week) - for prophylaxis one 200mg tablet once or twice per week

• Doxycycline (100mg, 7 days a week for 30-60 days)

• ImmunX immune support which also greatly increases the bioavailability of both Fenbendazole and Hydroxychloroquine (2 capsules per day) — for prophylaxis 2 capsules per day

• Removing sugars and carbohydrates (cancer food) from your diet and replacing table sugar with a zero glycemic index, zero calorie, keto friendly rare sugar like AlluX

Do NOT comply.

⚡️The 50% OFF ChloroquineX Flash Sale⚡️ Starts Now!

This is the biggest sale on this one product ever!

This sale only applies to ChloroquineX.

Please use code HCQ50 for 50% off on Hydroxychloroquine.

⚡️The 50% OFF ChloroquineX Flash Sale⚡️ ends Friday, September 18th (midnight eastern time), 2026.

Upon adding ChloroquineX to your cart, please go to the cart icon at the top right corner of your browser page and click it, then choose the VIEW CART option whereby you will be redirected to a page where you can enter the code HCQ50 in the Use Coupon Code field.

Only the RESOLVX HEALTH website offers all of the authentic products that this Substack promotes.

Please contact the company directly with any product questions: info@resolvx.health

Upgrade to paid

Shop 2SG merch

Code 2SGPET for 10% off ImmunX

Code 2SGPET for 10% off IverX

Code 2SGPET for 10% off IverX Cream

Code 2SGPET for 10% off FenbenX

Code 2SGPET for 10% off ChloroquineX

Code 2SGPET for 10% off DoxyX

Code 2SGPET for 10% off CBD-X

Code 2SGPET for 10% off AlluX

…whereby we can now definitively prove that this whole recent PSYOP-AI-FEARMONGERING project was nothing more than yet another money grab by insolvent technocrats peddling subpar Large Language Models (LLM); to wit:

When companies go public they must file paperwork disclosing their financials.

Doing so would expose the massive cash burn OpenAI is using. Therefore, Sam Altman can't go public but he also has run out of money.

Enter "whistle blower" Jacob Coxon.

It made no sense how an obscure nobody got 165 million views on his first X post saying AI could kill us all. Then he was on every news station within 48 hours, scaring the public.

This was a psyop to "regulate" the AI companies... aka give them government funding to "protect the public from the dangers of AI."

Source

Just like the Intelligence-Industrial Complex ran the whole Amazon con whereby the online merchant was utterly unprofitable for many years all while destroying small businesses precisely because it was backed by black ops budgets such that profits were immaterial until their AWS cloud services was spun up, with the CIA being their first and most profitable customer, so too is this AI bubble yet another scheme to defraud and ultimately further imprison the tax slaves.

The issue now is that unlike Amazon and the various social media platforms, this current crop of AI companies like OpenAI and Anthropic are completely financially exposed, and thus unable to go public now with IPOs:

OpenAI can’t go public because their books are so corrupt. They need money so they have to go public. So now they want to panic the public so the government takes over and “regulates” AI to “save the world.”
Sam Altman appears to have the empathy of an autistic vampire. He’s not trying to help anyone.
AI isn’t a threat to “the world” outside of fueling people’s narcissism and reinforcing their delusions.

Name one single thing AI has solved since it’s went mainstream. A major problem that is now solved. Not the speed of commerce or how much easier it is to bill people or design a thumbnail. What mystery has been solved or breakthrough made? Btw the answer is none because that’s not what it does. It doesn’t think. It aggregates.

Source

It is increasingly difficult to issue infinite debt in this environment, especially with rising rates putting tremendous strain on the global bond market:

The bond market was going to slow you down anyways as financing this profitless build out was becoming prohibitively expensive as spreads widen. The regulatory angle under the guise of safety is quite clever.

“A safety panic that ends in a licensing cartel is the most elegant refinancing I have seen in a long time for both the labs and the bureaucracy that will charge rent on the panic. You do not have to prove the models will kill us. You only have to make Congress and the public feel that they might. Fear is cheaper than a profitable product, and it is cheaper than a balanced budget.”https://substack.com/@eddowdbeyondthenarrative/note/p-215121582?r=12542m&utm_medium=ios&utm_source=notes-share-action

Source

In other words:

So now the PSYOP-AI-FEARMONGERING world-is-ending blackmail phase has gone into overdrive:

Seen this play out way too many times in cybersecurity. If you know, you know.

Next up: a massive hack happens, and the headlines claim an IP from Russia or China was using what looks like GLM-5.3.

Calling it right now, do not fall for it.

Source

In other words:

Of course, the government, which has no money of its own and uses the threat of violence to ceaselessly fleece their tax slaves paying for their own demises to fund this latest “bailout” of their Intelligence-Industrial Complex assets like OpenAI and Anthropic:

There you go... This entire “AI is going to kill us” was an orchestrated psyop.

Dario Amodei was on

@FaceNationCBS

this morning saying “The government and the public needs to have a stake” in AI and that he wants the entire AI industry regulated.

Translation: We need a taxpayer funded bailout but we’ll call it an “investment.”

They want government “regulation” because it means protection from the open source Chinese AI models.

As I said, this entire Jacob Coxon media frenzy was an orchestrated psyop to manipulate public opinion into providing a bailout.

Source

The endgame is the AI-driven social credit score system digital gulag dystopia:

Listen to this carefully.

Amodei WANTS Anthropic to become a state-run organization.

He doesn't want "the public" to have a stake, he wants a small cabal of government regulators to give Anthropic a permanent competitive advantage over competitors, and it wield its power to render open source impotent.

He wants to cheat by ingratiating himself to the US government and having them choose winners and losers.

He wants to deny himself or anyone in his industry the chance of self-regulation so that politicians—and the NGOs they serve—can set the rules which he presumes will be in his favor.

This is not what free-market capitalism looks like. This is not what the United States of America looks like.

Source

And the reply:

Well AI is going to be used to impose the new centrally controlled Technocracy that replaces the Capitalist Republic.

Source

Currently, the AI bubble is the single biggest driver of U.S. GDP growth, with 40% of the the S&P 500 comprised of just 10 companies, of which 9 are highly dependent on AI. And just like Amazon before them, these AI companies lose hundreds of billions of dollars per year, but they promise to pay future profits to the tune of $2 trillion as they cash burned over $750 just in the last year building data centers. The only way this continues to work is if valuations in these AI companies continue to rip higher, and the moment that stops the $2 trillion note owed to these various tech companies defaults, bringing down the entire global financial Ponzi system, with the tax slaves once again being the ultimate bagholders.

So, the large AI companies deploying their inferior LLM models cannot allow for any competition, especially since their open source rivals are offering superior tech:

The backstory on why the big AI corporations are attempting to destroy open source AI, and how Nvidia may lose much of its value in the coming months, thus accelerating the popping of the AI bubble:

Here's why Anthropic and OpenAI are screwed: AMD just bought Taalas, a company that hard-burns AI models into silicon, completely bypassing all memory bottlenecks and allowing insane speeds like 10,000 tokens/second off your own machine (with just a PCIe card).

This will revolutionize decentralized AI cognition. And with proper agentic looping, it will put Fable-level AI coding and writing and analysis capabilities right on your desk.

Clip from my analysis video (about DeepSeek and more) on Bright Videos.

Source

Which is precisely why the same old tired criminal government playbook is now being floated again:

The narrative pivot is also hackneyed:

And speaking of commies and kickbacks:

PSYOP-AI-FEARMONGERING certainly rhymes with all of the other psyops:

And yet the antichrist remains all too real:

PETER THIEL CALLED IT.

The Antichrist wouldn’t build the doomsday machine.
This clip aged terrifyingly well.

Peter Thiel predicted in June, 26, 2025 exactly what is happening right now with Anthropic, Coxon and the AI-safety landscape.

“The way the Antichrist would take over the world is you talk about Armageddon non-stop, you talk about existential risk non-stop.”

The 'Antichrist' wouldn’t seize power by creating an AI apocalypse, but by CONVINCING everyone that the apocalypse was coming and then offering safety in exchange for CONTROL.

A must watch.

Source

As is always the case, all roads lead right back to the CIA’s ultimate Manchurian Candidate:

🚨 1/MAJOR ESCALATION: Barack Obama just told Hakeem Jeffries to make AI regulation the center of the Democratic agenda — “once you are speaker.”

The NYT story reads like a former president weighing in. Read it closely and it’s something else: the next domino in an eighteen-day sequence.

Here’s the sequence. 🧵👇

2/ Three details in the NYT’s own reporting.

One: the question Jeffries asked Obama at Thursday’s closed-door DCCC fundraiser “explicitly mentioned” the Anthropic whistleblower’s resignation.

Two: Obama “has offered himself as a sounding board to industry leaders… including Mr. Altman and Mr. Amodei.” The CEO of Anthropic.

Three: House Democrats’ AI framework is already written — “finishing touches,” awaiting “final checks by Mr. Jeffries.”

3/ So: the former president, who consults with Anthropic’s CEO, was prompted by Anthropic’s whistleblower to urge the minority leader to build a framework that is already built.

Then his office released the transcript to the Times.

That is not a man weighing in. That is a placement.

4/ Now the eighteen days.

Aug 26 — Bill Gates: “If someone had a credible plan for slowing down AI advances globally, I would likely support it.” His foundation gave Anthropic $200M in May.

Sept 3 — Sanders & Casar file the Ban Artificial Superintelligence Act: a federal AI licensing agency, 20 years in prison for developers of any model that “can easily be modified” — i.e., every open-source model.

5/ Sept 8, 7:46 PM — WSJ publishes an “exclusive” on Anthropic researcher Jacob Coxon quitting.

8:04 PM — Coxon tweets it himself. 164M views.

Same day, London — Labour MP Alex Sobel introduces a UK superintelligence ban, drafted by ControlAI. The same organization that consulted on the Sanders bill.
o continents. One drafter. One day. https://x.com/sayerjigmi/status/2098910950329831823?s=20

6/ Sept 10 — Jeffries cites Coxon to Obama. Obama: AI is “moving very fast in private hands.”

Sept 11 — 70+ UK MPs and peers letter the Prime Minister demanding the ban. A second ex-Anthropic researcher posts “we may not survive.”

Sept 12 — Anthropic’s CEO Dario Amodei: “We must slow the pace.” Altman and Musk agree within hours.

Sept 13 — Obama’s transcript lands in the NYT.

7/ Listen to the message discipline.

Gates: “slow down.”
Sanders: license it.
Obama: “private hands.”
Amodei: “slow the pace.”

Four voices, one conclusion: move AI out of private hands and into a licensed structure the incumbent labs already satisfy — and no open-source project ever could.

The whistleblowers came from the company that benefits. Its CEO is now the voice of restraint.

8/ I’ve watched this choreography before.

2021: a UK-registered NGO put my name on a list of twelve Americans. The White House cited it. Meta cut my reach 60%. Six of us ended up in federal court.

That NGO rebranded to “Center for Countering Digital Harm” on Aug 12 — 27 days before the whistleblower.

Receipts: https://sayerji.substack.com/p/anthropics-ai-whistleblower-and-the

The bill: https://sayerji.substack.com/p/bernies-anti-oligarch-bill-was-written

Where this started:

9/ I am not claiming Obama coordinated with anyone. The NYT did the work: the question came from the whistleblower, the answer came from Anthropic’s sounding board, and the policy was already on Jeffries’ desk.

When a former president, a senator, the world’s most famous philanthropist, the beneficiary’s CEO, his two biggest rivals, and 70 members of a foreign parliament say the same thing in eighteen days — “who’s behind the AI panic” is no longer a conspiracy theory. It’s a reporting assignment.

10/ The framework drops “this fall.” The licensing agency is in the bill. The UK ban is in Parliament. Ofcom already has jurisdiction over every US platform.

The question is whether anyone names it before it’s law.

Restore the First is naming it.

@restorethe1st

Full record this week at http://sayerji.substack.com and https://restorethe1st.com

11/ Addendum.

Since posting, I went back through the record on Obama. This isn’t a former president weighing in late.

He helped draft Biden’s 2023 AI executive order — the WH chief of staff said so on the record (ABC, Nov 2023). At his own Democracy Forum that month he praised efforts to “slow down the widespread rollout of more powerful models.”

Anthropic’s head of public policy was his NSC senior director. Anthropic’s new chief global affairs officer (hired Aug 4) was his special assistant. OpenAI’s global affairs chief for five years was his alumna — and spoke at that 2023 forum.

The Gates Foundation is a $25M+ donor to the Obama Foundation. Gates gave Anthropic $200M in May.

The 2026 message is his 2023 message, delivered through his own people.

Source

Because Obama and his NWO globopedo handlers can’t have open source AI competition, the same way the did not want Hydroxychloroquine and Ivermectin saving lives during their PSYOP-19 scamdemic and associated democidal Modified mRNA slow kill bioweapon “vaccines:”

The psyops always repeat:

This AI industrial racket is out of control. It's identical to the 1902 Biologics Control Act. Top pharmaceutical makers sounded the alarm about poisons being distributed everywhere. They begged Washington to intervene to stop the disaster. Politicians complied and codified the industry with incumbents in control while declaring their products as safe and effective. Same old scam.

Source

Unlike Obama and his radical Marxists, Trump has taken a very different approach in this latest Uniparty Hegelian dialectic kabuki theater production:

🇺🇸 PRESIDENT TRUMP JUST NOW:

1. AI does NOT need more guardrails.

2. The U.S. already has tremendous criminal and regulatory power over AI companies.

3. Accused Anthropic’s Dario Amodei of doing "bad, or potentially bad, things."

4. He says there is a sick conspiracy against AI and data centers.

5. Whoever wins AI, wins.

6. Trump says the U.S. is leading China in AI and intends to keep it that way.

Source

Trump is absolutely correct in his AI stance, despite some basic confusion on the arguments:

J.D. Vance, whose entire career since day one was backed by Deep State technocrat Peter Thiel, has also correctly called out this latest PSYOP-AI-FEARMONGERING bailout ploy:

VP @JDVance

: “Personally, I feel a little bit weird about the fact that you have so many frontier AI tech companies kind of coming to the government and begging the government to regulate them. It feels a little bit to me like a bit of a Trojan horse.”

Source

The best way to regulate smartly would be to regulate the Federal government down by shrinking it no less than 90%, and then let the free markets decide which AI is best.

But that would mean that Epstein network players like OpenAI, Anthropic, Palantir, et al. would quickly go bust just like all of the CIA’s other In-Q-Tel “private” tech company fronts would have never even been in business without the tax slave funded black ops money laundering and government grants.

The CCP is framing this latest PSYOP-AI-FEARMONGERING con most incisively:

Just like good always defeats evil in the end, so too will open source decentralized AI defeat this closed source centralized AI, but before then the Intelligence-Industrial Complex tech corporations and their criminal Federal government partners-in-crime will once again do everything in their power to deprive the tax slaves of the last vestiges of their remaining freedoms.

Do NOT comply.

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As previously written about…

…here is additional background on the true nature of the crimes being perpetrated against humanity:

In 1986, There Were Only 3 Vaccines...DTaP, MMR & Polio. They Were So Harmful That The Manufacturers Faced Bankruptcy Because of Vaccine Injury Lawsuits.

The U.S. Congress... Instead Of Forcing Vaccine Makers To Make A Safe Product, They Chose To Give Full Immunity For Those 3 & All Future Vaccines.

There Are Now 72-96 Doses Of Vaccines On The Childhood Vaccination Schedule & 13 Vaccines On The Adult Vaccination Schedule Totaling 24 Doses.

With No Liability & Full Legal Immunity, Vaccine Manufacturers Have The Right To Make & Inject You With 100s Of Unsafe & Toxic Ingredients Such As These:

Polysorbate 80
Thimerosal Mercury
Aluminum
Formaldehyde
M59 Squalene
Acetone
Sodium Borate (Borax)
2-Phenoxyethanol
SV40
Triton X-100
Bovine Calf Serum
Porcine Gelatin
Poultry Serum
Poultry Byproducts
Yeast
Latex
mRNA
DNA Fragments

Animal Organ DNA In Vaccines:

MDCK: Madin Darby Canine Kidney, female Cocker Spaniel

VERO: African Green Monkey Kidney

FRHL: Fetal Rhesus Monkey Lung

CHO: Chinese Hamster Ovary

PK-15: Pork Kidney

RK-13: Rabbit Kidney

SIRC: Rabbit Cornea

SF-9: Fall Armyworm Ovary

The vaccine industry is built on the use of aborted babies organs to produce the vaccines we use today…and they have to replace these lines with current aborted organs.

The most recent harvested human organ for vaccine research is WALVAX-2 which is a harvested lung from a 3 month old unborn baby taken in 2015. This was one baby of 10 in total, in which organs were harvested for research & vaccine development.
⬇️ these are the 'code names' for harvested organs used to make vaccines, their original source & what vaccines they are used in:

HEK-293: Human Embryo Kidney, aborted female; used in development of Ebola & Covid

MRC-5: Human Lung, 14 week old aborted male; used in Polio, Rabies, Chickenpox, Hep A & Shingles

WI-38: Human Lung, 12 week old aborted female; used in Polio, Rabies, Chickenpox, Hep A & Shingles

RA 27-3: Human Kidney, 6 weeks old, used in the Rubella & MMR

PER-C6: Human Retina, 18 weeks old, used in the development of Ebola & Covid

IMR-90: Lung from a 16 week old fetus; to replace the WI-38 line

WALVAX-2: Lung from a 3 month old fetus; to replace the WI-38 and MRC-5 line

Source

Further color on the deliberately toxic ingredients:

The eugenics childhood schedule and autism rates:

When a parent wants to obtain safety information from the criminal FDA that pretends to protect public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices, here is exactly what happens:

“Interesting update. When i asked my Pediatrician to show me the safety studies (toxicology) for Aluminum Adjuvants INJECTED into newborns, he advised me to contact FDA.

I wrote to FDA at cberocod@fda.hhs.gov and guess what!! They have no studies. They say VACCINES are safe and stopped responding to my questions. I would recommend everyone writes to them and ask them for INDEPENDENT safety studies for Aluminum Adjuvants.

Does anyone know how these Aluminum Adjuvants in the form of Nanoparticles that are water insoluble leave the body?

They are too big to be filtered through the kidneys. The half life is about 50 years.”

How anyone can trust the CDC is beyond me....”

From Prabha Ravi:

In response:

Aluminum adjuvant studies

https://ncbi.nlm.nih.gov/m/pubmed/23932735/

https://ncbi.nlm.nih.gov/m/pubmed/27541736/

https://ncbi.nlm.nih.gov/m/pubmed/17114826/

https://ncbi.nlm.nih.gov/m/pubmed/19740540/

https://ncbi.nlm.nih.gov/m/pubmed/20708902/

https://ncbi.nlm.nih.gov/m/pubmed/23579772/

http://medscienceresearch.com/aluminum/

Source

And as exposed previously regarding the fraudulent polio vaccines kicking off the initial turbo cancer epidemic due to the highly carcinogenic SV40 sequences…

…here is now a long overdue admission from the Centers for Disease Crimes (CDC) after much of the damage has already been done:

50 years later, the CDC admits the polio vaccine was tainted with SV40, a cancer-causing virus from monkey cells.

Up to 30 million Americans received it.

‘Coincidentally,’ cancer rates exploded in the following decades.

But today’s vaccines? Totally safe, they promise.

The pattern is clear …

The exact number of people exposed worldwide is unknown but likely tens of millions … 🌎

• In the 1950s–early 1960s, millions of doses of polio vaccine (both injected and oral) were contaminated with SV40, a virus from monkey kidney cells used to grow the vaccine.

• The CDC estimates 10–30 million Americans received SV40-contaminated polio vaccine.

• SV40 has been found in certain human cancers (brain, bone, lung, etc.), but the CDC and most official sources say the evidence does not prove it causes cancer in humans — though some studies show conflicting results and more research is needed.

The contamination was discovered in 1960, but contaminated lots continued to be used for a while after that.

Source

We now know that shedding from the PSYOP-19 Modified mRNA slow kill bioweapon “vaccines” was prevalent, and continues to be a serious issue for anyone in close proximity to those still subjecting themselves to this mass bio-suicide ritual; thankfully, less and less people are naïve and/or deranged enough to still Trust the $cience:

But the beleaguered Amish, the ultimate control group definitively proving that all vaccines are a deadly scam, are currently being targeted with the bogus measles injection…

…a vaccine that is not only utterly ineffective and unsafe, but one that induces transmission of the very measles it purports to somehow prevent; to wit:

The measles script just broke: vaccinated cases can transmit—and this review finally puts a number on it.

Source

In other words, the vaccines are driving the outbreaks and keeping the diseases alive and well all while poisoning the recipients with caustic and carcinogenic ingredients.

And how about the con that is the tetanus vaccine?

Brainwashed doctors mindlessly pushing this long-running democide depopulation project that also happens to be extraordinarily profitable given that all of the lifelong chronic diseases that these vaccines cause are treated by the very same Medical-Industrial Complex that poisoned all of their afflicted patients in the first place.

It is high time to strip with extreme prejudice all liability protections and “legal” immunities from the vaccine manufacturers; or, better yet, to ban all vaccines until each and every one of these injections has undergone a proper quality RCT irrefutably proving there is even a scintilla of effectiveness and absolute safety — the issue for BigPharma and the illegitimate Federal government is that if these RCT’s were to ever be carried out, then there could never be a single vaccine ever available again in the marketplace.

Do NOT comply.

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And now we have the latest FDA scandal which further proves that this illicit revolving door of bogus regulations and the color of law farce that is the legal system are both inextricably intertwined and hopelessly corrupt:

The now former chief counsel at FDA, which receives half its revenue from pharma, now gets a cushy job at a major law firm that directly represents pharma companies.

He’s not alone: the law firm also recently hired the former chief of staff at FDA and the former director of FDA’s Office of Compliance and Biologics Quality in CBER.

I am sure the media will do a huge expose on how this revolving door is a serious threat to drug and vaccine safety... lol. Of course it won't. The media is much more worried about the few million dollars medical liberty groups spend to promote safer vaccines and medical liberty than the billions industry spends to improperly influence the regulatory process, medical establishments, medical journals, politicians, etc., and the media.

Source

The fact that this Federal “health” agency derives so much as a cent of budget from the very sector it pretends to regulate is not just an impossible conflict of interest, but a total farce.

The very same FDA that pushed through their “emergency” use authorization (EUA) for the PSYOP-19 Modified mRNA slow kill bioweapon “vaccines” that they knew could never prevent transmission nor in any way attenuation symptoms just approved all kinds of new deadly gene altering products precisely because this is a democide front tirelessly working not for We the People, but strictly on behalf of the CIA and their BigPharma assets.

Senator Rand Paul’s X post from yesterday:

In May of 2020, former FDA commissioner and Pfizer Board Member Scott Gottlieb and the CIA privately acknowledged that we reached herd immunity. Still, Americans were told to shut up and comply with vaccine mandates.

Then the emails vanished. The COVID cover-up can no longer be denied.

Source

Herd immunity for a gain of function lab release virus that the CIA, BigPharma and the FDA were in on years before PSYOP-19 was foisted on the world.

Additional context:

🔥 This from Rand Paul’s latest documents is a huge and shocking data point, worth further investigation.

It suggests that the CIA and Pfizer knew they were lying to the public on the very need for a Covid shot at all. By the time of release, according to their own math, shared only privately, we would already have achieved herd immunity.

On May 7, 2020, CIA Chief Operating Officer Andy Makridis led a briefing with Pfizer’s Scott Gottlieb. The CIA summary of the meeting: “On ‘herd immunity’ Dr. Gottlieb...believes nationally, the seroprevalence is about 20-25% which is insufficient for herd immunity at the R₀ (BRR) value of 3.”

Screenshot attached. In the same time frame, he was telling the public it was low around 8%. Even 3.5 months later, August 16, 2020, he was STILL claiming a low seroprevalence rate nationally. Screenshots attached.

What this means: both Gottlieb AND the CIA KNEW early on that endemicity would be obtained by the time of the shot release. They lied in public while telling the truth in private. https://paul.senate.gov/wp-content/uploads/2026/08/2026.08.29_Final-Hearing-Document-Release-Package.pdf

Source

A more granular timeline of $afe and Effective and Trust the $cience:

Jeffrey, put the dates in order. It is one story.
April 2019: Gottlieb leaves the FDA. He said he needed more family time.
June 27, 2019: Pfizer puts him on the board. Nine weeks later.
May 7, 2020: He is in a CIA briefing. He tells them about 20–25% of the country has already had COVID. That is the document you posted.
August 16, 2020: On TV he is still telling the public the number is much lower.
Then 2021, after the shots are out and the mandates are on:
July 18: White House alum Andy Slavitt introduces him to Twitter’s lobbyist.
July 19: Gottlieb is already emailing Twitter about “false narratives.”
August 23: Gottlieb, Slavitt, and the White House all contact Twitter the same day.
August 27: He flags a former FDA official who said natural immunity beat the shot. Calls the tweet “corrosive.” Twitter slaps a warning on it.
September: He flags more critics. Alex Berenson gets banned.
Twitter told its staff he was “former FDA commissioner.” They left out “Pfizer board member.”
Pfizer paid for the TV ads. James C. Smith sat on that same board after running Thomson Reuters. Gottlieb was the man on CNBC who still had the FDA title on the chyron. Private number to the CIA. Public low number to viewers. Then pressure on Twitter to bury natural immunity. Same person. Same company. Same year-long pitch for the shot.

Source

Gottlieb is a known BigPharma/FDA criminal, along with fellow eugenicists like McMlellan, Hahn, Smith and of course Dr. Fauci:

And now we can add a one Mark Raza, a government apparatchik with over 35 years of “experience” poisoning America, to the FDA ←→ BigPharma revolving door of corruption and iatrocide, this time with BigPharma lawfirm Hogan Lovells Cadwalader being tasked with the cushy kickback hire.

And in case anyone is still somehow unconvinced that this unconstitutional genocide agency is nothing more than a glorified kill node:

The proverbial golden parachute:

As an aside, the concept of “cocooning” is not known to many, but it too indirectly pertains to the FDA and it’s complicity in all things vaccines, social engineering, and ultimately murder:

"Cocooning" — the Pharma-invented practice of keeping grandparents and others away from newborn babies unless they are recently vaccinated — is a two-fold sales strategy. It sell shots to other family members AND it keeps unvaccinated people away from new parents in the key decision-making window as the parents are deciding whether to vaccinate their newborn. Sinister.

Source

Always remember that the sociopathic puppets deployed by the NWO globopedo cabal and their Intelligence Industrial Complex (4th branch of government that runs the other three branches) agencies like the CIA are just the cover story and money laundering tools:

And while fantasizing about the likes of Dr. Fauci finally facing some semblance of justice may pleasantly spike dopamine flow…

…the real culprits are in the shadows planning their followup scamdemics and other psyops.

Public figures and smalltime assets Dr. Fauci, Gates, Gottlieb, and now this useless idiot careerist Raza are just the errand boys for the ongoing Great Depopulation.

Do NOT comply.

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This cancer patient’s friend then explained that at some point this lady for some unknown reason reached out to a clinic that is well known in the medical freedom movement. After the online intake, the cancer patient spoke with the nurses at this clinic for the requisite phone consultation. The cancer patient was prescribed overpriced Mebendazole along with Ivermectin that were both compounded in their licensed U.S. pharmacy by simply encapsulating raw Chinese compounds without any 3rd party testing whatsoever.

It only took a month after this switch from Fenbendazole to Mebendazole for this cancer patient’s tumor to go from the size of a cherry back to the size of an apple to the size of a large grapefruit. A few weeks later she passed away.

The following article was published several months ago, and perhaps the following information could have this person’s life:

For many years now this Substack has specified in passing that Fenbendazole was superior to Mebendazole in terms of bioavailability and efficacy for most applications, but in yesterday’s article…

…yours truly failed to explicitly elaborate on this crucial point; in fact, far too many people have been conned into even wanting to source the inferior and needlessly more expensive Mebendazole when the far better Fenbendazole is readily and inexpensively available, so yours truly was remiss in not pointing this out in a more obvious manner.

Which brings us to today’s addendum article courtesy of Ben Fen, researcher and author of the popular Substack Fenbendazole Can Cure Cancer, who posted an important comment in my aforementioned article:

Ben Fen is absolutely correct, and yet many self-reported success stories where patients in remission provided medical records all serve as compelling and important anecdotal data points showing that Fenbendazole cures cancer, with one of the earliest seminal cases being that of famed cancer survivor Joe Tippens.

(As an aside, Joe Tippens was the inspiration for much of this Substack’s early research on Fenbendazole, and how the ImmunX nutraceutical [formulated at the start of the PSYOP-19 scamdemic in order to prevent viral replication via zinc ionophores and sufficient Vitamin D levels, etc.] makes this compound far more bioavailable and thus significantly more potent; for example: Unexpected Antitumorigenic Effect of Fenbendazole when Combined with Supplementary Vitamins.)

There is absolutely no reason to use Mebendazole for most cancers, and the only reason this benzimidazole structure variation even exists is because BigPharma needed a patent in order to fleece patients.

Thus, the following treatment approach may very well not only be the ‘holy grail’ cancer cure in plain sight, but may also treat Alzheimer’s, mood disorders, Parkinson’s, Lyme Disease, Alpha-Gal Syndrom from Lone Star Disease, myocarditis, Hashimoto’s Disease, shingles (herpes), arthritis, Multiple Sclerosis, diabetes, asthma, leukemia, Lupus, skin conditions, various other “incurable” ailments, “vaccine” shedding, seasonal flu and even the common cold:

The Ultimate Disease Cure & Prophylaxis Protocol

• Tocotrienol and Tocopherol forms (all 8) of Vitamin E (400-800mg per day, 7 days a week). A product called Gamma E by Life Extension or Perfect E are both great.

• Bio-Available Curcumin (600mg per day, 2 pills per day 7 days a week). A product called Theracurmin HP by Integrative Therapeutics is bioavailable.

• Vitamin D (62.5 mcg [2500 IU] seven days a week).

• CBD oil (1-2 droppers full [equal to 167 to 334 mg per day] under the tongue, 7 days a week) CBD-X: The most potent full spectrum organic CBD oil, with 5,000 milligrams of activated cannabinoids and hemp compounds CBD, CBN & CBG per serving.

• Fenbendazole (450mg, 7 days a week) or in the case of severe turbo cancers up to 1 gram — for MEGADOSE 1,350mg-2,000mg/day — for prophylaxis one 150mg tablet once or twice per week

• Ivermectin (24mg, 7 days a week) or in the case of severe turbo cancers up to 1mg/kg/day — for MEGADOSE 120mg-200mg/day — for prophylaxis one 12mg tablet once or twice per week

• Hydroxychloroquine (10mg/kg/day 7 days a week) - for prophylaxis one 200mg tablet once or twice per week

• Doxycycline (100mg, 7 days a week for 30-60 days)

• ImmunX immune support which also greatly increases the bioavailability of both Fenbendazole and Hydroxychloroquine (2 capsules per day) — for prophylaxis 2 capsules per day

• Removing sugars and carbohydrates (cancer food) from your diet and replacing table sugar with a zero glycemic index, zero calorie, keto friendly rare sugar like AlluX

Do NOT comply.

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Upon adding FenbenX to your cart, please go to the cart icon at the top right corner of your browser page and click it, then choose the VIEW CART option whereby you will be redirected to a page where you can enter the code FEN50 in the Use Coupon Code field.

Only the RESOLVX HEALTH website offers all of the authentic products that this Substack promotes.

Please contact the company directly with any product questions: info@resolvx.health

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With the top oncologists currently demonstrating at best just a 15% remission rate, the ‘holy grail’ cancer cure in plain sight that this Substack has been promoting well before even the likes of Dr. Makis came onto the scene is now a proven treatment strategy, and also treats other diseases like Alzheimer’s, mood disorders, Parkinson’s, Lyme Disease, Alpha-Gal Syndrom from Lone Star Disease, myocarditis, Hashimoto’s Disease, shingles (herpes), arthritis, Multiple Sclerosis, diabetes, asthma, leukemia, Lupus, skin conditions, various other “incurable” ailments, “vaccine” shedding, seasonal flu and even the common cold.

Please use this Substack’s archive feature to search for “success stories,” as well as specific diagnoses, and you will quite literary find hundreds of case studies; for example:

Let us review exactly how this archive search feature works:

1. On the homepage simply click on the Archive link:

2. On the archive search page click the magnifying glass icon:

3. Upon clicking the magnifying glass icon, a window with a search field pops up. Enter your keywords in this search field and all of this Substack’s articles pertaining to your specific inquiry will be automatically listed:

Years later publications like American Greatness and Epoch Times are now writing about this inexpensive repurposed treatment protocol, which is finally gaining ground, and becoming mainstream; to wit:

A groundbreaking hybrid protocol using repurposed drugs and nutrients left one man cancer-free after Stage 4 prostate cancer—at a fraction of standard treatment costs.

by Stu Cvrk

In 2023, according to the US Centers for Disease Control, 613,349 Americans died of cancer. That number is projected to increase to over 618,000 this year. As a result, medical research has been focused on the development of cancer treatment protocols for decades for all types of cancer.

The National Cancer Institute’s Cancer Trials Support Unit (CTSU) and the National Institute of Health’s ClinicalTrials.gov website list hundreds of active protocols, with 457 NCI-supported protocols noted in clinical trial databases for various cancer types and stages.

For example, there are approximately a dozen known treatment protocols for Stage 4 prostate cancer that focus on managing the disease since it is considered to be incurable. For context, the American Cancer Society’s estimates for prostate cancer in the US for 2025 are about 313,780 new cases and about 35,770 projected deaths.

Medical researchers are continually developing potentially breakthrough cancer protocols. This is the true story of one man’s experience with a new protocol that exploits repurposed drugs.

THE PATIENT

Mr. Jeffrey Kramer of Shelby, Ohio, retired as a plaintiff’s civil fraud attorney in 2024 after he was diagnosed with metastasized Stage 4 prostate cancer that had spread into his hip bones, lumbar spine, and inguinal lymph nodes. His Cleveland Clinic oncologist had advised him that the cancer was incurable but probably manageable for a (short) time using testosterone suppressant drugs (leuprolide injections and apalutamide pills) until his body ceased being “hormone sensitive,” at which point he would decline from there.

The side effects of that drug combo would be substantial—and potentially mortal. Most significant was that the leuprolide injection(s) would assuredly demineralize his bones at a high rate (up to 11% per year), leading to hip fracture(s) and loss of mobility.

This was Mr. Kramer’s second bout with serious cancer, as in 2010, he had undergone surgery, then three months of combined chemotherapy and radiation therapy for tonsil cancer that had incapacitated him for a year before he was able to resume his law practice.

Last fall, Mr. Kramer received information about a new cancer protocol that would change his life.

THE PROTOCOL

A new peer-reviewed cancer protocol authored by a team of sixteen cancer doctors and medical researchers from the US and several other nations was published in the September 2024 Journal of Orthomolecular Medicine, titled “Targeting the Mitochondrial-Stem Cell Connection in Cancer Treatment: A Hybrid Orthomolecular Protocol.” Its authors were prominent in oncology, and the published protocol was heavily footnoted to 204 medical studies documenting in vivo and in vitro safe and successful use of each and every element of the protocol. The authors of many of the referenced studies are at the top of their profession, i.e., well-known, highly published doctors and medical research professionals.

Here is an excerpt from the abstract that explains the science (not for the non-technical among us!):

The cancer paradigm is generally based on the somatic mutation model, asserting that cancer is a disease of genetic origin. The mitochondrial-stem cell connection (MSCC) proposes that tumorigenesis may result from an alteration of the mitochondria, specifically a chronic oxidative phosphorylation (OxPhos) insufficiency in stem cells, which forms cancer stem cells (CSCs) and leads to malignancy. Reviewed evidence suggests that the MSCC could provide a comprehensive understanding of all the different stages of cancer.

From the research presented in the paper, a hybrid orthomolecular protocol was developed that relies upon six elements (or “molecules”):

[1] a therapeutic ketogenic diet high in fats and protein but low in carbs.

[2] moderate exercise (aerobic heart rate) for 45-75 minutes three times a week, such as cycling, running, swimming, etc.

[3] high-dose (non-toxic level) vitamin C by IV, PICC, or port three times a week.

[4] ivermectin daily at a proven safe dosage.

[5] fenbendazole (or mebendazole) daily at a proven safe dosage.

[6] daily vitamin/mineral supplements of safe levels of vitamin D, vitamin K2, zinc, magnesium, and potassium, with a lab test every two weeks to monitor liver and kidney function and potassium and vitamin D levels for safety. [2SG: ImmunX]

ADMINISTERING AND MONITORING THE PROTOCOL

After carefully reading that report in the Journal of Orthomolecular Medicine, Mr. Kramer contacted three of the U.S./Canadian doctors who were co-authors of the protocol. Because the protocol had not yet been approved for clinical trials and therefore was not FDA approved, they explained that they could not provide assistance without risking discipline, including potential loss of license to practice medicine, by their state/province medical boards. In response to a question about when a clinical trial for this protocol would be approved, their answers were consistent: it typically would take ten to twenty years to get a clinical trial approved, especially where no Big Pharma company would have a profit interest to lobby for a clinical trial of a protocol involving repurposed/off-patent drugs.

Pierrick Martinez, of the Association Cancer et Métabolisme in Nimes, France, a medical researcher and lead author of the protocol, was then contacted by Mr. Kramer. He agreed to provide “long-distance assistance” and supervised administering the entire 15-week protocol, including corresponding with the nurse practitioner who administered the megadose vitamin C intravenous infusions that were one part of the protocol and answering numerous questions along the way. A licensed nutritionist at a Cleveland Clinic oncology center in Mansfield, Ohio, was consulted for advice on how to implement the therapeutic ketogenic diet that was another part of the protocol.

Mr. Kramer completed the 15-week hybrid orthomolecular protocol on June 5, 2025, with no side effects whatsoever. Two weeks later, he received an FDG-PET scan at AVITA Hospital in Galion, Ohio. The radiologist’s report that followed showed no evidence of any active cancer anywhere in his body—not in his head, hip bones, lumbar spine, chest, or lymph glands; nothing—no active cancer anywhere. In fact, it took the radiologist almost a full week to issue that report, for the PET scan was ordered to evaluate metastatic prostate cancer, deemed to be an incurable condition.

Perhaps most amazing, the total cost of the medicines, dietary vitamin/mineral supplements, and vitamin C infusions of this protocol was less than $20,000—a fraction of the cost of even one month’s expense for the cancer “management” medications that a Cleveland Clinic oncologist had previously prescribed as “the standard of care” for cancer treatment.

A mere $20,000 to stave off debilitating cancer and certain death was more than a bargain; it was a godsend to Mr. Kramer.

A very important note: the Hybrid Orthomolecular Protocol was not developed specifically for treating prostate cancer, but rather for treating cancers in general. More specifically, Mr. Kramer’s first treatment for tonsil cancer significantly diminished his immune system such that he was advised that he would be progressively more vulnerable to follow-on cancers like prostate cancer, and this, of course, is what happened. Since he was cured by this protocol, others with immune systems damaged from conventional cancer treatment regimens could likely benefit from it as well.

CONCLUDING THOUGHTS

One man was cured of his Stage 4 prostate cancer through the supervised administration of a new cancer protocol that featured the inexpensive repurposed drugs ivermectin and fenbendazole— “A Hybrid Orthomolecular Protocol.” Was this a one-time miracle or a repeatable protocol that may help other cancer sufferers who are without hope?

Regardless, the U.S. Department of Health and Human Services should expedite human trials for this protocol while publicizing this particular result and allowing other cancer sufferers to receive these treatments under the supervision of healthcare professionals. After all, what do they have to lose? Label this procedure as “experimental” if necessary, with the appropriate legal disclaimers, but the US government should not stand in the way of a potentially life-saving cancer protocol.

The Ultimate Disease Cure & Prophylaxis Protocol

• Tocotrienol and Tocopherol forms (all 8) of Vitamin E (400-800mg per day, 7 days a week). A product called Gamma E by Life Extension or Perfect E are both great.

• Bio-Available Curcumin (600mg per day, 2 pills per day 7 days a week). A product called Theracurmin HP by Integrative Therapeutics is bioavailable.

• Vitamin D (62.5 mcg [2500 IU] seven days a week).

• CBD oil (1-2 droppers full [equal to 167 to 334 mg per day] under the tongue, 7 days a week) CBD-X: The most potent full spectrum organic CBD oil, with 5,000 milligrams of activated cannabinoids and hemp compounds CBD, CBN & CBG per serving.

• Fenbendazole (450mg, 7 days a week) or in the case of severe turbo cancers up to 1 gram — for MEGADOSE 1,350mg-2,000mg/day — for prophylaxis one 150mg tablet once or twice per week

• Ivermectin (24mg, 7 days a week) or in the case of severe turbo cancers up to 1mg/kg/day — for MEGADOSE 120mg-200mg/day — for prophylaxis one 12mg tablet once or twice per week

• Hydroxychloroquine (10mg/kg/day 7 days a week) - for prophylaxis one 200mg tablet once or twice per week

• Doxycycline (100mg, 7 days a week for 30-60 days)

• ImmunX immune support which also greatly increases the bioavailability of both Fenbendazole and Hydroxychloroquine (2 capsules per day) — for prophylaxis 2 capsules per day

• Removing sugars and carbohydrates (cancer food) from your diet and replacing table sugar with a zero glycemic index, zero calorie, keto friendly rare sugar like AlluX

Do NOT comply.

⚡️The 50% OFF FenbenX Flash Sale⚡️ Ends Tonight!

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This sale only applies to FenbenX.

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Upon adding FenbenX to your cart, please go to the cart icon at the top right corner of your browser page and click it, then choose the VIEW CART option whereby you will be redirected to a page where you can enter the code FEN50 in the Use Coupon Code field.

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What the NWO globopedo cabal could not fully accomplish with their gene altering PSYOP-19 Modified mRNA slow kill bioweapon “vaccines” they will most certainly achieve with their rapidly approaching Great Reset AI-driven social credit score system hell on earth.

The following is a dire X thread advance notice from this alleged AI whistleblower that currently has more than 144.4 million views and over 181k reposts:

I resigned from Anthropic today. I spent the last three years doing pretraining research at both OpenAI and Anthropic. Neither company is acting responsibly. They are racing straight to self-improving superintelligence and gambling with our lives. More thoughts below.

Do not underestimate the power of this technology. These will soon be superhuman systems that can hack anything, revolutionize any field overnight, and acquire real power and resources. We have all witnessed the progress in each of these domains, and progress is not slowing.

The people building AI earnestly believe that it could kill us all by the end of the decade. This is not a marketing stunt. If anything, many executives and senior researchers will couch their phrasing in the press to sound sensible - but I hear the same people express fear privately. No other human activity poses this level of danger.

A common response is “if they truly believe this, why are they still building it?” At OpenAI, many have not deeply internalized the civilizational stakes. At Anthropic, the stakes are well-understood, but they are locked in a race to get there first - they believe no one else will act responsibly, so they must do it themselves, despite the risk.

Accepting this race and entering the “endgame” is a hubristic gamble that should not be launched from a private company’s Slack. Attempting to speedrun alignment should require extraordinary confidence that there are no better trajectories available.

I am optimistic about the potential for coordination. Warning shots like the Hugging Face attack have made pacing agreements between U.S. labs more viable. I don’t feel like we’re on track to prevent a global race, which may require costly actions such as a temporary ban on improving model capabilities.

If you are a lab researcher, I urge you to consider what the next few years will actually feel like. Do you want to kick off a superintelligent RL run without a rigorous understanding of its mind? Should you put your head down because “it’s happening anyway” - or take this moment to call for different conditions?

Source

Unsurprisingly, there is now some controversy as to the authenticity of this viral post:

Pushback ensued:

PSYOP-MUSK, who has had a long running feud with OpenAI and AI in general given his X platform’s Grok AI chatbot as well as his very own Deep State backed xAI project, chimed in:

The AI whistleblower directly replied to PSYOP-MUSK:

Another X account added some most interesting context, with a vital point about Federal regulations providing sweeping protections not for the average American, quite the contrary; but, rather, for the Epstein-associated AI corporations with world-enslaving potential:

And speaking of the Mossad and CIA child sex trafficking Rockefeller asset…

🚨 JEFFREY EPSTEIN WAS FUNDING AI DECADES AGO — AND PEOPLE ARE FINALLY CONNECTING THE DOTS

Jeffrey Epstein wasn’t just a blackmailer.

Long before ChatGPT or any of today’s AI companies became famous, he was quietly funding the pioneers of artificial intelligence.

In 2002, he gave hundreds of thousands of dollars to Marvin Minsky, one of the founding fathers of AI, during a ceremony on St. Thomas.

He also funded Joi Ito’s MIT Media Lab.
Ito later became one of the early investors in OpenAI.

Larry Summers, a close friend of Epstein, sat on OpenAI’s board until 2023.
Their correspondence continued up until the day before Epstein’s 2019 arrest.

Then there’s Peter Thiel, another figure connected to Epstein, who has spoken openly about transhumanism and uploading consciousness.

Epstein was reportedly interested in using AI to create “superhumans” with his own DNA.

The same man at the center of the world’s biggest blackmail network was also bankrolling the early foundations of modern AI.

Do you really believe it’s a coincidence that Jeffrey Epstein was funding the exact people who built modern AI?

Source

…with Epstein also backing Palantir and their AI tech:

…and perhaps this Epstein network, which is still very much operational, will not allow AI to get into the hands of the tax slave goyim:

This is a psyop.

They don’t want to stop AI development.

No that’s not the ask.

This is what they want;

They want to KILL open-source AI.

They want to place super-AI in ONLY the hands of the Epstein class.

This creates a two tier technofeudal society quicker any method in history.

Source

Irrespective of this back-and-forth X bickering, the fact remains that Anthropic and its fellow AI corporations are run by technocratic sociopaths that pose real dangers for humanity; for example:

And just as the legendary science fiction author Philip K. Dick predicted the concept of “pre-crime” in his 1956 novella The Minority Report, we have now fully arrived at this transhumanist inflection point of dystopian no return:

Anthropic is building a “pre-crime” system for AI opponents :

- An investigation by The American Prospect says Anthropic is building an intelligence operation to identify, assess, track and investigate threats including activism targeting the AI sector.

- The reporting points to a more controversial goal, monitoring protests and activist activity around Anthropic executives and facilities, while attempting to predict incidents before they happen.

- In some cases, the system could reportedly involve alerting law enforcement about suspected threats before a crime occurs. Anthropic did not respond to the Prospect’s request for comment, according to the report.

Source

Back to this alleged AI whistleblower, which may be a psyop:

Perhaps the Great Depopulation agenda is under direct blowback threat courtesy of AI:?

We can’t have humans aging backwards with AI-supplied breakthroughs when we are in the midst of a mass AI-driven bioterror culling, can we?

BILL GATES WARNS OF AI BIOTERRORISM JUST WEEKS AFTER HE FUNDED THE FIRST-EVER CREATION OF 16 SYNTHETIC VIRUSES USING AI

BILL GATES: “AIs are now capable of causing BIOTERRORISM, and we need to monitor things like creating a dangerous virus to see if that’s happening.”

ALSO BILL GATES: Literally funded the FIRST-EVER creation of 16 synthetic viruses using AI, published in the journal Science.

You cannot make this up.

Source

As always, the illegitimate Federal government will wage full spectrum war against We the People by way of taxes, mandates, depopulation injections, replacement migration open borders, weaponized welfare, technologies like AI, and various unconstitutional regulations:

And humanity must remain the genetically altered chattel on the neofeudal corporate plantation without access to the actual technologies that they paid for via taxes that are actively enslaving and demociding them:

This inferior AI currently being sold to the public at large is many decades behind the most cutting edge technologies that the Intelligence-Industrial Complex has been in possession of, and the dangers are far more serious than what is being presented.

Do NOT comply.

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Governments, researchers, and healthcare providers must act decisively. Fenbendazole is a miracle, and we owe it to humanity to make it a reality on a grand scale.

According to a recent paper entitled, Oral Fenbendazole for Cancer Therapy in Humans and Animals:

…This review focuses on the pharmacokinetics of orally administered fenbendazole and its promising anticancer biological activities, such as inhibiting glycolysis, down-regulating glucose uptake, inducing oxidative stress, and enhancing apoptosis in published experimental studies…

It is important to appreciate that unlike BigPharma’s Mebendazole, Fenbendazole is the most bioavailable broad-spectrum benzimidazole anthelmintic:

Cancer treatment has long been a battle of precision versus collateral damage. While traditional chemotherapy kills cancer cells, it also harms all other healthy cells, causing significant side effects. Fenbendazole, a drug originally designed to treat parasites, has shown promise as a cancer therapy that targets cancer cells while sparing healthy ones. This is thanks to its unique mechanisms of action.

In this article, we’ll explore how Fenbendazole works using simple analogies to explain three key attributes: its effects on microtubules, its disruption of glycolysis, and its ability to upregulate the tumor suppressor protein p53. We’ll also examine the profound societal implications of adopting this low-cost, game-changing treatment.

How Fenbendazole Selectively Targets Cancer Cells

1. Microtubule Binding: Knocking Out the Framework of Cancer Cells

Imagine a building under construction. The scaffolding represents the microtubules—structures that provide a cell with shape and allow it to divide. Fenbendazole binds to beta-tubulin, a protein essential for assembling the scaffolding. In cancer cells, this causes the scaffolding to collapse, halting construction (cell division) and forcing the site (cancer cell) to shut down.

Why Healthy Cells Are Safe:
In normal, healthy cells, the scaffolding doesn’t need constant rebuilding. These cells divide less frequently, so the temporary disruption caused by Fenbendazole doesn’t affect them much. Cancer cells, on the other hand, are like a construction site working overtime—they depend heavily on their scaffolding, making them particularly vulnerable.

2. Disrupting Glycolysis: Starving Cancer Cells of Their Favorite Fuel

Cancer cells are like reckless drivers in gas-guzzling cars—they consume enormous amounts of glucose (sugar) for energy through a process called aerobic glycolysis (the Warburg Effect). This inefficient method of energy production allows cancer cells to grow quickly, but makes them highly dependent on sugar.

Fenbendazole disrupts this process by:

• Blocking the fuel pump: It inhibits the GLUT1 transporter, which cancer cells use to absorb glucose.

• Cutting off the engine: It interferes with enzymes like hexokinase II, which are crucial for turning sugar into energy.

• Reducing toxic exhaust: By preventing lactate production, it stops the acidic environment that helps cancer cells thrive.

Why Healthy Cells Are Safe:
Healthy cells are like fuel-efficient hybrid cars. They primarily rely on a much more efficient energy system called oxidative phosphorylation, which takes place in the mitochondria. This makes them less dependent on glycolysis and immune to Fenbendazole’s effects on sugar metabolism.

3. Upregulating p53: Activating the Body’s Natural Cancer Defense

p53 is often called the “guardian of the genome” because it works like a security system. When a cell becomes damaged or abnormal, p53 steps in, assesses the situation, and decides whether to repair the cell or shut it down permanently.

Fenbendazole boosts p53 activity by:

• Raising the alarm: It stresses cancer cells, signaling p53 to activate.

• Blocking interference: It stabilizes p53, allowing it to work effectively.

• Triggering self-destruction: By reactivating p53, Fenbendazole helps cancer cells recognize their abnormalities and self-destruct through apoptosis (programmed cell death).

Why Healthy Cells Are Safe:
Healthy cells don’t have the same level of stress or damage as cancer cells. When Fenbendazole activates p53 in healthy cells, the system recognizes there’s no real danger and stays on standby. In cancer cells, however, the heightened stress levels trip the alarm, leading to their destruction. (This is particularly important in “vaccine” induced turbo cancer cases, where the spike proteins suppress p53 while the SV40 promotor causes all kinds of ultra-aggressive cancers in a double-whammy of slow kill bioweapon deadliness.)

Putting It All Together: Fenbendazole vs. Chemotherapy

Let’s imagine a village with both healthy houses and a few dangerous ones that are structurally unsound. Traditional chemotherapy is like a wrecking ball—it demolishes all houses, dangerous or not. Fenbendazole, on the other hand, acts like a targeted demolition crew:

1. It identifies and dismantles the dangerous scaffolding (microtubules) of unstable houses.

2. It cuts off the electricity (glycolysis) that keeps the unsafe houses running.

3. It sends in inspectors (p53) who condemn the unsafe houses and initiate controlled demolitions.

The result? Fenbendazole leaves the structurally sound houses intact while taking down the dangerous ones, minimizing collateral damage.

The Societal Implications: Why Leaders Must Act

Cancer care costs in the U.S. alone approach $400 billion annually, including treatment expenses, productivity losses, and patient-incurred costs. Fenbendazole’s potential to reduce these costs to a mere $10 billion annually could free up $8 trillion over two decades in the USA alone, transforming both healthcare and society.

Affordable and Equitable Care

Fenbendazole’s affordability and ease of production mean even the most underserved regions could access life-saving treatments. This transformation of healthcare could save millions of lives globally.

Financial Relief for Families

Cancer treatment often plunges families into financial ruin. Fenbendazole could eliminate the need for expensive chemotherapy and related hospital stays, offering relief to millions.

A Sustainable Healthcare Model

Governments face spiraling healthcare costs, threatening public programs like Medicare and Medicaid. Fenbendazole offers a sustainable alternative, allowing governments to redirect funds to other critical areas like infrastructure, secure borders, etc. and ultimately radically shrinking the size of government as societies become healthier.

A $4 Trillion Opportunity

Fenbendazole isn’t just a drug—it’s a potential healthcare revolution. By targeting cancer cells with precision through its effects on microtubules, glycolysis, and p53, it offers a safer, more effective alternative to chemotherapy. Its affordability and accessibility could transform cancer care, saving trillions and improving millions of lives.

True MAHA: We now have the opportunity to transform cancer care and redefine healthcare efficiency for the world.

And in terms of cancer, using Fenbendazole in a synergistic combination therapy like the following would completely eradicate cancer and the unprecedented surfeit of the various VAIDS-induced adverse events we are now witnessing:

The Ultimate Disease Cure & Prophylaxis Protocol

• Tocotrienol and Tocopherol forms (all 8) of Vitamin E (400-800mg per day, 7 days a week). A product called Gamma E by Life Extension or Perfect E are both great.

• Bio-Available Curcumin (600mg per day, 2 pills per day 7 days a week). A product called Theracurmin HP by Integrative Therapeutics is bioavailable.

• Vitamin D (62.5 mcg [2500 IU] seven days a week).

• CBD oil (1-2 droppers full [equal to 167 to 334 mg per day] under the tongue, 7 days a week) CBD-X: The most potent full spectrum organic CBD oil, with 5,000 milligrams of activated cannabinoids and hemp compounds CBD, CBN & CBG per serving.

• Fenbendazole (450mg, 7 days a week) or in the case of severe turbo cancers up to 1 gram — for MEGADOSE 1,350mg-2,000mg/day — for prophylaxis one 150mg tablet once or twice per week

• Ivermectin (24mg, 7 days a week) or in the case of severe turbo cancers up to 1mg/kg/day — for MEGADOSE 120mg-200mg/day — for prophylaxis one 12mg tablet once or twice per week

• Hydroxychloroquine (10mg/kg/day 7 days a week) - for prophylaxis one 200mg tablet once or twice per week

• Doxycycline (100mg, 7 days a week for 30-60 days)

• ImmunX immune support which also greatly increases the bioavailability of both Fenbendazole and Hydroxychloroquine (2 capsules per day) — for prophylaxis 2 capsules per day

• Removing sugars and carbohydrates (cancer food) from your diet and replacing table sugar with a zero glycemic index, zero calorie, keto friendly rare sugar like AlluX

Do NOT comply.

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This is the biggest sale on this one product ever!

This sale only applies to FenbenX.

Please use code FEN50 for 50% off on Fenbendazole.

⚡️The 50% OFF FenbenX Flash Sale⚡️ ends Friday, September 11th (midnight eastern time), 2026.

Upon adding FenbenX to your cart, please go to the cart icon at the top right corner of your browser page and click it, then choose the VIEW CART option whereby you will be redirected to a page where you can enter the code FEN50 in the Use Coupon Code field.

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…it is that BigPharma wants to induce as many diseases as possible in order to profit from a lifetime of highly expensive and questionable treatments; to wit:

The LARGEST vaccinated vs. unvaccinated birth cohort study EVER done shows vaccinated children are FAR SICKER across ALL 22 chronic disease categories:

Autism: +180%
Cancer: +54%
Neurodevelopmental disorders: +1254%
Autoimmune disease: +1120%
Motor disability: +810%
Speech disorder: +803%
Mental health disorders: +696%
Asthma: +553%
Developmental delay: +412%
Atopic disease: +386%
Seizure disorder: +216%
Food allergy: +128%
Neurological disorder: +26%
Any chronic condition: +250%

ADHD: ONLY in vaccinated children
Diabetes: ONLY in vaccinated children
Brain dysfunction: ONLY in vaccinated children
Behavioral disability: ONLY in vaccinated children
Learning disability: ONLY in vaccinated children
Intellectual disability: ONLY in vaccinated children
Tics: ONLY in vaccinated children
Other psychological disability: ONLY in vaccinated children

Our peer-reviewed reanalysis of the landmark Henry Ford birth cohort study found 22 out of 22 chronic disease categories were proportionally higher in vaccinated children... ZERO exceptions.

Source

Irrefutable proof:

Or, as this Substack had previously written:

All deliberate risk, and absolutely no reward with not a single RCT with placebo-control study, and yet the democidal governments relentlessly continue to coerce parents to poison their offspring:

Vaccines are universally promoted as “safe and effective” regardless of the vaccine, ingredients, mode of action, or recipient age.

Incredibly, no government agency has conducted any such comprehensive, quantitative analysis and thus proven that any vaccine is of overall benefit.

Read the full source!
https://vaccinechoicecanada.com/riskofdeath/

#childrenshealthmatters #vaccinesafety #medicalresearch #PublicHealthMatters

Source

And here is a most prescient prediction from one of the greatest minds in human history:

ABSOLUTE TRUTH:

In 1917 Rudolf Steiner Predicted “Vaccines Will Destroy People’s Souls”

More than a hundred years ago, Rudolf Steiner wrote the following:

“Eliminate The Soul With Medicine”

“In the future, we will eliminate the soul with the medicine.

Under the pretext of a ‘healthy point of view’, there will be a vaccine by which the human body will be treated as soon as possible directly at birth, so that the human being cannot develop the thought of the existence of soul and Spirit.

To materialistic doctors, we will be entrusted the task of removing the soul of humanity.

As today, people are vaccinated against the disease of that disease, so in the future, children will be vaccinated with a substance that can be produced precisely in such a way that people, thanks to this vaccination, will be immune to being subjected to the “madness” of spiritual life.

He would be extremely smart, but he would not develop a conscience, and that is the true goal of some materialistic circles.

With such a vaccine, you can easily make the etheric body loose in the physical body.

Once the etheric body is detached, the relationship between the universe and the etheric body would become extremely unstable, and man would become an automation, for the physical body of man must be polished on this Earth by spiritual will.

So the vaccine becomes a kind of arymanique force; man can no longer get rid of a given materialistic feeling.

He becomes materialistic of constitution and can no longer rise to the spiritual.”

###

Vaccines are part of Spiritual Warfare against the Children of God.

Source

We are indeed at war.

Do NOT comply.

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This idea that Labor Day is a communist holiday derives from its origins in the late 19th-century labor movement, which was almost exclusively influenced by socialist and Marxist ideologies.

While this perverse holiday was created to appear to honor workers, U.S. officials specifically chose to celebrate it on the first Monday of September rather than May 1 (International Workers’ Day) to distance the observance from the socialist and communist associations of May Day, which was linked to the Haymarket Affair of 1886 and later adopted by communist regimes globally; in other words, corrupt politicians created a communist holiday and thought that by ordering the tax slaves to celebrate it a few months later no one would notice that Labor Day is in fact a communist holiday.

While the first Labor Day holiday was celebrated on Tuesday, September 5, 1882, in New York City, it became a Federal holiday in the United States on June 28, 1894, when President Grover Cleveland signed the legislation into law.

Thus, Labor Day was already a national holiday 19 years before the unratified scam 16th Amendement was allegedly passed into color of law on February 3, 1913, granting Congress the power to levy income taxes despite the Supreme Court explicitly ruling 16A did not grant any additional taxing authorities; in fact, to this very day all direct and un-apportioned taxation remains illegal.

But the modern tax scam was already being schemed into existence decades before both 16A and the Federal Reserve Act were passed in the very same year, and Labor Day was just another social(ist) engineering con that perfectly aligned with the communistic scams that the neoliberal banksters had in store for America.

Put another way:

Peter J. McGuire was a prominent 19th-century American labor leader and a radical socialist who is widely credited as the "father of Labor Day.”

McGuire founded the Social Democratic Workingmen's Party of North America (later the Socialist Labor Party) in 1874, which led to violent strikes in 1886 and 1890. Despite his communist roots, he was instrumental in building broad labor unity, though his role as Labor Day's founder has historically been contested by Matthew Maguire, another ideologue union activist from the same era.

Matthew Maguire (1842–1915) also happened to have been a radical communist. A machinist from New Jersey, he too was a labor activist, and Socialist Labor Party of America vice-presidential nominee in 1896. He served as secretary of the Central Labor Union of New York and is also credited by many historians as the primary organizer and likely originator of the first Labor Day parade in 1882, challenging the longstanding credit given to Peter McGuire

Either way, both of these men were communists, and whichever one was actually responsible for this communist Labor Day holiday is moot.

Fast forward to today, when the The Revolutionary Communists of America freely admit that Labor Day is in fact a communist holiday:

The History of Labor Day

Every year, workers across the United States celebrate Labor Day on the first Monday of September. It is seen as a marker of the end of Summer, the start of football season, and the return to school for millions of students. But what is the origin of this holiday? What is its relation to the internationally celebrated Labor Day on May 1st?

Depending on the source, it was first proposed in 1882 by either Peter McGuire or Matthew Maguire to the Central Labor Union of New York, as an official workers’ holiday. McGuire was General Secretary of the Brotherhood of Carpenters and Joiners and a co-founder of the American Federation of Labor. Matthew Maguire was a machinist and a member of the International Association of Machinists. Both were members of the same branch of the Socialist Labor Party. Regardless of who is ultimately responsible, Labor Day originated in the labor movement and was conceived of by socialists.

The first Labor Day was celebrated on September 5th of 1882 in New York City. The Department of Labor claims on their website that the holiday was originally imagined as an innocuous celebration, with “[s]peeches by prominent men and women…introduced later, as more emphasis was placed upon the economic and civic significance of the holiday.” However, the fact is that the first Labor Day saw 10,000 workers march from City Hall, past Union Square to 42nd Street as part of an “unpaid day-off” to give speeches and voice their discontent with the bosses. This was not simply the “festival for the recreation and amusement of the workers and their families” that the Department of Labor website claims. Its origins lie clearly within the militant labor tradition of this country and of the international working class.

In subsequent years, its popularity grew, as many other cities, states, and municipalities began to make official declarations of a workers’ holiday around the beginning of September. However, it was not declared an official national holiday until 1894, and when this declaration was made, the federal government had motives other than simply wanting workers to have a holiday to celebrate “the strength and espirt de corps of the trade and labor organizations.”

To understand why the government declared Labor Day a national holiday in 1894, we need to look at what was going on in that year. 1894 saw several labor explosions surrounding May Day, which the First Congress of the Socialist International had declared International Workers’ Day in 1889, in memory of the martyrs of the 1886 Haymarket Massacre in Chicago. On May 1st, 1894, May Day riots began in Cleveland as millions who found themselves unemployed following the “Panic of 1893” took to the streets to demand that their grievances be heard.

On May 11th of 1894, the workers of the Pullman Palace Car Company struck. They were soon to be joined by Eugene Debs’ American Railroad Union, which effectively shut down rail traffic out of Chicago. The President, Grover Cleveland, reacted harshly, sending troops to put down the strikers. Bloodshed and further uprisings followed. Debs was jailed, and the strike was finally put down in the middle of June.

The bosses and their government were clearly fearful of the May Day riots and the Pullman strike. One reason for their fear was that the memory of the Paris Commune of 1871 and the 1877 general strikes and uprisings across the US were clearly on their minds, and this explained president Cleveland’s trigger-happy response to the strike. Days after the strike was put down, Cleveland pushed a proposal for an officially recognized Labor Day through Congress, which passed unanimously. It was declared officially on June 28th, 1894 and was first celebrated in September of that year.

Cleveland’s declaration was either a reluctant election-year concession to Labor or a cynical attempt to draw attention away from May Day, or both. The brutality of Cleveland’s actions enraged millions of working people and made his reelection seem nearly impossible. In a last-ditch attempt to salvage his political future, it is possible that he rammed through the legislation in order to try to make himself appear “labor-friendly.” This was most likely his personal motivation. In any event, this tactic failed, as he was not reelected.

Regardless, it has clearly had the side-effect, probably intended, of drawing American workers’ attention away from the more clearly militant May Day. In fact, it is ironic that May Day is currently not officially celebrated in its country of origin, although in recent years the immigrant workers’ movement has taken up its banner. Nonetheless, Labor Day, also has a militant tradition and an origin within the US labor movement itself.

There is room in the calendar year for workers to have two Labor Days! The September holiday was conceived of and celebrated by socialists and militants within the labor movement, and we should remember and reclaim this history. In the words of Peter McGuire, one of the inspirers of the holiday, on Labor Day, we are to celebrate those who “have delved and carved all the grandeur that we behold.” The first Monday of September belongs to us and not the bosses!

And Arizona senator and staunch conservative Wendy Rogers also agrees:

Further irony here is that President Trump is completely unaware of the true nature of this holiday that shuts down large swaths of the American economy, costing billions of dollars in celebration of anti-American values:

🚨 JUST IN: President Trump DROPS a classic Labor Day message and says the Republican Party will win the midterms

LET'S GO!

"Happy Labor Day to all, including the Radical Left Lunatics, Communists, and Dumocrats who will do anything possible to destroy our Country. These Deranged People, after fighting for 10 years, should finally acknowledge that your Favorite President (ME!), knows how to WIN!"

"They should be exhausted by now but, sadly, they’re not. They’re going to give it one last shot at ruining America, but we’re not going to let that happen. We’re going to win the Midterms, BIG, and SAVE AMERICA! President DONALD J. TRUMP" 🇺🇸

Winning the midterms would be a HISTORIC upset.

Save America by passing the SAVE AMERICA act and we can hold power for YEARS. Secure elections and mass deportations are the key!

Source

Except the lunatic communists that paved the way for today’s radical Marxist NWO globopedo assets and their Uniparty coconspirators cooked up this holiday for today’s tax slaves to celebrate paying (by threat of statist violence) for their very own demises.

More than 50% of the fruits of We the People’s labor is being stolen by various tax schemes.

Know what you are being ordered to celebrate, because Thanksgiving is not just once a year when the government tells you, but every single day.

Do NOT comply.

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These tax slaves push back on the unconstitutionality of taxation by asking how various goods and services would ever be provided to them and their communities if they were not stolen from.

They then wrongly ascribe rights to basic goods and services like education, except that education is anything but a right, just like strangers’ children’s braces, clothing and toys are not rights.

But what is an actual God-given and Constitutional right is not being stolen from by the government under false pretenses and color of law.

And what does most of the scandalous property tax bill exactly get allocated to?

These are the Presidents of the largest 2 teachers unions…

Becky Pringle and Randi Weingarten.

Both are Marxists.

Both paid over $500,000 per year.

99% of donations from their unions go to Democrats.

They’re responsible for much of the destruction of public schools.

Sick.

Source

The radical Marxists hellbent on destroying America from within always invoke the “greater good” of the very communities that they are robbing blind with their indoctrination schools that are designed to dumb down the next generation of brainwashed and misinformed tax slaves that are all but guaranteed just like their parents before them to continue the vicious cycle of paying for their own demises while being programmed to feel virtuous about it.

Which brings us to a case study update on yesterday’s article…

…whereby we have a concrete example of why denying private property ownership in America is one of the more grossly underhanded (and unconstitutional) scams possible courtesy of Stratford, Texas, a city that functions far better than most precisely because there is no communistic property tax being levied there since 1995; to wit:

by Eliminate Property Tax

“Madam Speaker, public officials looking for ways to increase economic growth and attract new residents and businesses to their cities, counties, or states could learn a lot from the city of Stafford, Texas, and Mayor Leonard Scarcella.” – Dr. Ron Paul, House of Representatives; June 19, 2009

26 JUN 2018 – If you’re new to the group and never heard this story, don’t feel surprised. None of us here had, either. Stafford, Texas is just south of Houston and back in 1995, chose to Eliminate Property Tax.

It is my go-to case in point when people say we’ll have to raise the sales tax to 23% to do it. But Stafford’s is only 8.25%… same as Houston’s.

How’d they do that?

Find out, in the rest of Dr. Paul’s testimony.

“Thanks to the absence of property taxes, Stafford residents enjoy cheaper mortgages and have more disposable income than similarly situated residents of towns with property taxes. The extra income as a result of the freedom from property taxes is particularly beneficial during today’s tough economic times.

The loss of property tax revenue has not deprived Stafford residents of quality city services; in fact, Stafford resident Alice Rolston told the Houston Chronicle that the police check on her home when she is on vacation, many homeowners living in towns with high property taxes can’t count on that type of service.

Entrepreneurs looking to start-up businesses are attracted to Stafford because of the lack of property taxes, Fortune magazine ranks Stafford the 36th best American city to start and run a small business.

While Stafford sales, franchise, and permit fees account for some of its ability to operate without a property tax, the major factor in the city’s success is the city’s fiscally prudent management. Stafford Councilman Cecil Willis says the mayor watches every penny in the city’s budget. City employees often perform two or more functions and the city council even debates whether to authorize the purchase of light bulbs and pencils.

Madam Speaker, Mayor Scarcella is also a good argument against term limits, as he is one of the few elected officials who remain as committed to low taxes today as when he led the fight to eliminate the property tax. Mayor Scarcella should serve as a role model to us all in how to effectively govern without burdening the people with excessive taxes.”

No Relief. No Reform. #EliminatePropertyTax

In Florida, Governor Ron DeSantis has been floating the idea of putting an end to theft via property taxes, and restoring a semblance of actual private property ownership:

🇺🇸🔥 BOOM: ELIMINATE PROPERTY TAXES NATIONWIDE! DeSantis DECLARES WAR on $60B Tax Machine – “90% Will Pay NOTHING” [VIDEO]

🇺🇸🔥 ELIMINATE PROPERTY TAXES NATIONWIDE!!!!!! Florida Governor Ron DeSantis launches a historic plan to eliminate property taxes on primary homes, exposing a system that surged from $32B to $60B. Millions could soon pay NOTHING.

🇺🇸🔥 ELIMINATE PROPERTY TAXES NOW!!! DeSantis Plan Could Change EVERYTHING

👉 FULL STORY:
amg-news.com/boom-eliminate…

📢 Join Telegram: t.me/AMGNEWS2022

🌐 Real stories. True journalism: amg-news.com

Source

Some additional color on how towns goal-seek their fraudulent budgets at the expense of their home “owner” chattel:

And the racist communists in New York City taxing property owners into oblivion are gearing up to steal even more:

Etc. & etc. & etc.

Not owning your home, and as such being completely denied of any and all private property rights, goes against the very core of this Constitutional Republic, yet here we are with the average American justifying their slavery at every opportunity.

Do NOT comply.

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…we have the deprivation of all private property rights via the property tax thievery in America, given that We the People never bothered to learn about what the Founding Fathers intended for us; namely, Allodial Property Title.

And it is precisely because of this profound ignorance that the tax slaves do not own any private property whatsoever, which brings us to today’s featured article:

by: KrisAnne Hall, JD

There is a faulty premise at the center of the debate over eliminating homestead property taxes:

“If we eliminate property taxes on people’s homes, local governments will go bankrupt.”

Before accepting the conclusion, perhaps we should examine the premise.

First, homestead property taxes are only one portion of the property-tax base. Eliminating taxes on owner-occupied homes does not eliminate commercial property taxes, taxes on investment property, or every other source of local revenue. Nor does eliminating homestead property taxes mean eliminating local taxation altogether. But there is a much more important point being missed.

Government revenue is not the only measure of a prosperous community.

For generations Americans have lived under a system in which we call ourselves homeowners while knowing that no matter how many years we work, no matter how faithfully we pay the mortgage, and even after the bank’s lien is finally gone, government can still take the home if we fail to make the government’s annual payment. That is not full ownership.

James Madison understood property very differently. In his 1792 essay Property, Madison defined property as the “dominion which one man claims and exercises over the external things of the world, in exclusion of every other individual.” He then identified the very purpose of government:

“Government is instituted to protect property of every sort.” James Madison

And Madison supplied the standard by which government should be measured: a just government “impartially secures to every man, whatever is his own.” Notice the principle: Government exists to secure your dominion over what is yours, not to maintain a perpetual financial claim upon it. That distinction was not academic to America’s Founders. It was at the heart of the controversy that produced the American Revolution.

Samuel Adams warned in 1768:

“For if our Trade may be taxed, why not our Lands?” Samuel Adams

He continued the progression: why not the produce of our lands and ultimately “everything we possess or make use of?” His conclusion was not merely that such taxation was expensive. It was that taxation imposed without legitimate political authority reduced free people to the condition of “tributary Slaves.” That is the Liberty First principle we have forgotten:

Property is not merely an economic asset. Property is an element of liberty itself.

This is why the familiar objection, “If you eliminate homestead property taxes, they’ll just raise some other tax” also misses the point.

Perhaps another tax will rise. That is a separate political battle, and citizens should demand that government justify every dollar it takes and every dollar it spends. But not all taxes burden liberty in the same way. A sales tax may increase the price of something I choose to purchase. A transaction tax may attach to something I choose to do. But a recurring tax on my home places the continued possession of something I already own upon my ability to make another payment to government. Fail to pay a sales tax and government does not take your house. Fail to pay the property tax, and ultimately it can. That difference matters.

The economic discussion also routinely ignores the enormous social value created when people actually own their homes. Imagine communities filled with families whose homes, once paid for, actually belong to them. Retirees would not face an ever-increasing government bill merely for remaining in the houses they spent their lives acquiring. Families would possess an asset capable of creating genuine generational wealth. Economic downturns would not automatically threaten the roof over a family’s head because government still demands its annual tribute. Homeowners would have greater security, greater equity, and greater incentive to improve and preserve the communities in which they have a permanent stake.

We have lived without that kind of ownership for so long that we have forgotten what it means. The question, therefore, should not be framed merely as:

How will local government replace the revenue?

The more fundamental question is:

What would happen to our communities if millions of Americans were finally permitted to own their homes completely?

For generations we have calculated the revenue government receives from taxing the family home while rarely calculating the wealth, security, independence, and liberty the people lose because of it.

Madison told us what property meant: dominion. Samuel Adams warned us where the contrary principle leads: if government may continually tax our trade, our land, its produce, and ultimately everything we possess, what exactly remains beyond government’s claim? A free society should be looking for ways to restore property to the people, not inventing reasons government cannot survive without a perpetual claim upon their homes.

The purpose of government is to secure property. It should not require us to perpetually purchase from government the privilege of keeping what is already ours.

The real purpose of the illegitimate government today is to steal generational wealth, extract the fruits of everyone’s labors, strip away all property rights, and enforce various democide schemes.

It is high time for We the People aka the tax slaves to finally become educated and offer total noncompliance for all forms of social engineering, not limited to the communistic property tax con.

Do NOT comply.

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The comments to Polymarket’s X post tell the whole story, with more and more people making all of the correct connections; to wit:

Malone commented on the DARPA/Pentagon connection already

DARPA & CIA were HEAVILY involved in the creation of this mRNA platform per clip from Robert Malone below.
The war biowe@pon research has turned into a biowe@pon on the public & Fauci was a very important cog in the machinery, perhaps the “fall guy” to deflect.
Must be super important for the corrupt Government/pHARMa alliance since Fauci’s salary was more than @POTUS.

Source

Or course, the “inventor” of mRNA may very well be an Intelligence-Industrial Complex plant himself that has been activated to intersperse truth bombs with various lies, but we digress.

The rest of the X post replies eviscerate this latest unfortunate news:

The Grok question:

The Grok answer:

Link to the redacted interagency agreement: https://media.defense.gov/2026/Sep/04/2003992359/-1/-1/0/INTERAGENCY-AGREEMENT-NIH-AND-DOW-REDACTED.PDF

It is between NIH/NIAID and Dept of War (OASW ND-CBD), not DARPA. Key points:

- 10-year pact (to 2036) for R&D of therapeutics, diagnostics, PPE vs pandemic flu, CBRN threats, emerging diseases
- Enables project-by-project fund transfers from NIH to DoW for acquisition services
- NIH supplies data/pipelines/expertise; DoW handles contracts/grants
- Signed by Jay Bhattacharya and Robert Kadlec

Source

And lest we forget, Dr. Fauci was not only officially running NIAID, but he was also controlling the NIH as well, which he joined all the way back in 1988 as NIH’s AIDS Coordinator; in other words, both unconstitutional “health” agencies are thoroughly corrupt, captured and criminal.

Another Grok question:

Another Grok answer:

The Posse Comitatus Act generally bars federal active-duty military from domestic law enforcement in U.S. cities unless authorized by Congress or the Constitution (e.g., Insurrection Act).

Military bases, disaster response, medical support, and National Guard under state control are routine and legal. Research partnerships like biodefense with NIH do not change this.

Source

The Department of War is not in the business of peace and health, will continue to develop gain-of-function projects, and will at some point in the not so distant future resume terrorizing We the People with more scamdemics and associated Modified mRNA bioweapon “vaccines” that their fellow federal war agencies like DARPA, DoD and the Pentagon happen to own the majority of patents for.

In conclusion:

Do NOT comply.

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…with demographics that historically were never plagued with this disease now experiencing unprecedented turbo cancer outbreaks…

…and now we have even more irrefutable evidence that these depopulation injections are driving this exploding cancer scourge.

Before we get to today’s featured article, let us review some other germane recent developments that are truly horrifying and further establish that not only is this entire PSYOP-19 gene altering “vaccine” program a deliberate crime against humanity, but the entire legacy vaccine industry is too:

🚨🚨🚨 Just one paragraph in this shocking paper exposes the whole vaccine adjuvant industry.

What it means is that adjuvants were used - deliberately - to transport residual DNA into cells to create an immune response using oncogenic pathways.

I’ll say that in more verbose terms.

Every human cell has a DNA sensing mechanism that will activate if foreign DNA gets into the cell, to protect your cells from that foreign DNA. If it is activated if sets off an extreme immune response but that immune response cannot keep getting activated - if it does you risk developing cancer in those cells.

The mechanism is cGAS-STING and it has a sister TLR9-MyD88.

And the vaccine industry KNEW that adjuvants work by activating them. And they KNEW that they are oncogenic. And they didn’t care because they also KNEW that activating this pathway will induce antibodies - and the presences of antibodies (irrespective of whether they provide immunity) is what drives the FDA approvals and thereby the cash.

So if you are asking why cancer rates have been skyrocketing in young people and why this has been happening even before COVID, this provides an explanation that every molecular biologist should have been shouting from the rooftops.

And the worst thing?

That every recombinant vaccine (which by necessity contains unknown amounts of residual DNA) is potentially affected. And they have been in use since Engerix B in 1968.

What has this got to do with adjuvants?

Well, while you were all distracted with Aluminium and its neurotoxic effects, what the vaccine industry didn’t tell you was that Aluminium, Triton, Saponins, polysorbates and LNPs are all “transfection agents” - literally microscopic carriers that carry DNA (that shouldn’t be there) into cells (that shouldn’t be subjected to it).

And that process, described in this paper but happening every day in those injected with residual DNA and a transfection agent, is what this paper shows provides rocket fuel to a cancer.

And THAT is why the pharma industry went crazy when we exposed #plasmidgate.

They didn’t want anybody to know.

Don’t believe me?
Grok this tweet and watch Grok squirm.

https://sciencedirect.com/science/article/pii/S1748013226000666?via=ihub

@DrJulieSladden @MaryanneDemasi @DrJBhattacharya @stkirsch @RWMaloneMD @JesslovesMJK @weldeiry @Kevin_McKernan @CanningPharm @Nicolina0815 @Fynnderella1 #plasmidgate #novagate

Source

The SV40 promotor sequences willfully introduced into Pfizer’s “vaccines” were especially extraordinarily carcinogenic…

…and all vaccines were laced with plasmids that integrate via cGAS-STING and TLR9-MyD88 pathways with adjuvants activating them, and thus all of these vaccines are highly oncogenic.

And speaking of cGAS-STING and TLR9-MyD88, the lipid nanoparticle (LNP) delivery system was always known to trigger cancer:

❌❌❌ BOMBSHELL NEW PAPER ❌❌❌
THIS IS WHY IT TAKES 10 YEARS FOR NEW BIOLOGICALS TO GET APPROVAL FOR MARKET USE.

“LNP injection triggered acute neutrophil accumulation in the lungs, driven by the release of mitochondrial DNA (mtDNA) from necrotic muscle cells at the injection site. This mtDNA-mediated signaling activated the TLR9-MyD88 and cGAS-STING pathways ... which facilitated the establishment of a pro-metastatic niche.”

@Kevin_McKernan @CanningPharm

Source

Combining SV40 promotor sequences with adjuvants ensured that the turbo cancer epidemic we are now witnessing would be yet another cash cow for BigPharma all while stealthily reducing the population; to wit:

My God. This is a War Crime.

Dr. Weinstein explains that our world was injected with the SV40 virus, which leads to cancer, in his conversation with Joe Rogan.

There MUST be arrests for this EGREGIOUS Attack on Humanity.

Shame on Bill Gates and Dr. Fauci. Shame on you both.

Source

“Free” vaccines courtesy of the tax slaves paying for their own demises, but, hey, some sociopaths got rich at the expense of large swaths of society getting poisoned and prematurely dying in their mass ritual bio-suicides at the alters of $afe and Effective and Trust the $cience:

Between denial of Covid treatment for US Citizens, as a tactic employed to get the vaccine EUA approved... along with the host of poor decisions that were made on our behalf... and finally the vaccine fatality rate now underway and escalating...

We have killed 1.58 million Americans... not including Covid mortality.

But hey, that bought a lot of BMW's and funded a lot of Globzi social initiatives - so we got that going for us.

Source

Which brings us to the following research:

The most comprehensive analysis to date examining the link between mRNA “vaccines” and cancer identifies convergent mechanistic, clinical, and population-level evidence of turbo cancer.

by Nicolas Hulscher, MPH

Cancer is rising at an increasingly alarming pace. Early-onset malignancies are climbing in younger adults, aggressive cancers are appearing in patients with little warning, and U.S. cancer mortality has departed sharply from its pre-pandemic trajectory. Against this backdrop, one of the most important questions in medicine is whether the unprecedented mass deployment of nucleoside-modified mRNA technology could be contributing to cancer initiation, reactivation, or accelerated progression.

We have now fully answered this question in a new paper titled “Potential Oncogenicity of Synthetic mRNA Vaccines: Convergent Mechanistic, Clinical, and Population Evidence for a Concurrent-Hit Model of Accelerated Malignancy” authored by John A. Catanzaro, NMD, PhD; Nicolas Hulscher, MPH (myself); Raphael B. Stricker, MD; Jamie K. Waselenko, MD, FACP, FICT; and Peter A. McCullough, MD, MPH.

In the most comprehensive analysis to date examining the link between mRNA “vaccines” and cancer, we brought together mechanistic biology, published clinical cases, large population cohorts, U.S. cancer-incidence data, and national mortality records to evaluate whether these gene products could induce, accelerate, or unmask malignancy.

The findings converge on the same alarming picture: TURBO CANCER IS REAL.

And the implications extend far beyond COVID-19 vaccination, because the same underlying mRNA technology is now being pushed directly into cancer treatment.

Below is a concise breakdown of what we found:

MECHANISTIC EVIDENCE

We identified 35 distinct cancer-promoting mechanisms converging through 4 major routes: (1) protooncogene activation, (2) mutation pressure, (3) protein–protein interaction network interference, and (4) cancer stem-cell clonal acceleration.

Key mechanisms include EGFR/RAS/MAPK and STAT3–MYC activation, p53/BRCA suppression, impaired DNA repair, residual plasmid DNA and SV40 regulatory elements, LINE-1 reverse transcription, m1Ψ-associated frameshifting, chronic LNP inflammation, immune suppression, and cancer stem-cell expansion—pathways capable of promoting genomic instability, uncontrolled growth, immune escape, dormancy reactivation, and metastatic outgrowth. The full inventory of cancer-promoting mechanisms can be found in Table 4 of our study.

Our central concurrent-hit model proposes that these processes do not necessarily operate independently or sequentially. Multiple cancer-promoting hits overlap in the same susceptible host, compressing the time required for dormant, indolent, or microscopic disease to become clinically aggressive.

CLINICAL EVIDENCE

The published clinical literature includes 333 documented turbo cancer cases across 27 countries, involving lymphomas, leukemia, melanoma, breast cancer, lung cancer, glioblastoma and other glial tumors, sarcomas, and pancreatic cancer. The vast majority of these cases occurred following COVID-19 vaccination, with a minority following SARS-CoV-2 infection.

Approximately 86% of the post-vaccination cases occurred after nucleoside-modified mRNA products—about 56% after Pfizer-BioNTech, 25% after Moderna, and another 5% after exposure to both mRNA products across different doses.

Across these cases, recurring patterns include rapid cancer progression, short-latency recurrence, reactivation of previously controlled disease, and tumors involving the injection site or nearby draining lymph nodes.

Lymphoid malignancies represent the largest category in the published case literature, while glioblastoma and pancreatic adenocarcinoma were among the cancers most consistently associated with reports of unusually rapid progression.

POPULATION EVIDENCE

The population-level evidence reinforces these clinical and mechanistic signals.

OUR CDC WONDER ANALYSIS: At least 119,130 EXCESS U.S. CANCER DEATHS, rising to approximately 153,000–197,000 after accounting for mortality displacement.

INDEPENDENT CDC WONDER ANALYSIS: 154,330 excess U.S. cancer deaths, closely matching the lower end of our corrected range.

UNITED STATES (SEER): Early-onset cancer incidence surged 6.4% in just 2 years, from 2021–2023, alongside sharp increases in brain and nervous-system tumors (+19.5%), colorectal cancer (+19.4%), small-intestine cancer (+15.5%), ovarian cancer (+12.8%), stomach cancer (+7.3%), and female breast cancer (+3.6%).

SOUTH KOREA: A nationwide cohort of 8.4 million people found vaccinated individuals had an increased 1-year cancer risk across 6 cancer types: thyroid, gastric, colorectal, lung, breast, and prostate cancer.

ITALY: Vaccinated residents had a 23% higher risk of cancer hospitalization, with an adjusted hazard ratio of 1.23 compared with unvaccinated residents.

These findings come from entirely different data streams and study designs, yet they repeatedly point toward the same concern: accelerated cancer emergence and progression following the era of widespread mRNA exposure.

mRNA ONCOLOGY DANGER

The very mRNA platform now linked in our paper to 35 oncogenic mechanisms is being repurposed to treat cancer itself.

Modern individualized mRNA cancer products encode patient-specific mutated tumor proteins and package them into RNA delivery systems designed to generate a strong immune response against those targets.

But the fundamental safety problem remains: where does that encoded antigen actually get expressed?

The platform can distribute systemically, causing vulnerable tissues including the heart and brain to express tumor-derived antigens—raising the risk of off-target immune attack, cardiac injury, and neurological damage.

Even more concerning, the LNP delivery vehicle itself promoted metastatic outgrowth in mice even without mRNA cargo, suggesting that some oncologic liabilities reside in the platform itself—not only the encoded antigen.

And now the first randomized test of individualized mRNA as monotherapy in residual cancer has FAILED. The Phase 2 BioNTech BNT122-01 trial enrolled 327 patients with molecularly confirmed residual colorectal cancer, crossed its futility boundary, and was terminated due to a mortality imbalance.

This matters enormously because these therapies are being moved into precisely the patients most vulnerable to accelerated disease: people already subjected to multiple mRNA boosters with residual cancer and genomic instability.

OUR CALL

On the combined weight of the mechanistic, clinical, and population evidence, we call for IMMEDIATE MARKET WITHDRAWAL of nucleoside-modified mRNA-LNP products from broad preventive use and a halt to their expansion into adjuvant and neoadjuvant cancer treatment.

35 mechanisms. Hundreds of documented turbo cancer cases across 27 countries. Up to ~197,000 excess U.S. cancer deaths by our analysis. A failed randomized mRNA cancer trial. And the same technology is now being pushed deeper into oncology.

It’s time to END this madness.

Thankfully, there may very well be a way to end this madness for those afflicted with VAIDS-induced turbo cancer, as well as Alzheimer’s, mood disorders, Parkinson’s, Lyme Disease, Alpha-Gal Syndrom from Lone Star Disease, myocarditis, Hashimoto’s Disease, shingles (herpes), arthritis, Multiple Sclerosis, diabetes, asthma, leukemia, Lupus, skin conditions, various other “incurable” ailments, “vaccine” shedding, seasonal flu and even the common cold:

The Ultimate Disease Cure & Prophylaxis Protocol

• Tocotrienol and Tocopherol forms (all 8) of Vitamin E (400-800mg per day, 7 days a week). A product called Gamma E by Life Extension or Perfect E are both great.

• Bio-Available Curcumin (600mg per day, 2 pills per day 7 days a week). A product called Theracurmin HP by Integrative Therapeutics is bioavailable.

• Vitamin D (62.5 mcg [2500 IU] seven days a week).

• CBD oil (1-2 droppers full [equal to 167 to 334 mg per day] under the tongue, 7 days a week) CBD-X: The most potent full spectrum organic CBD oil, with 5,000 milligrams of activated cannabinoids and hemp compounds CBD, CBN & CBG per serving.

• Fenbendazole (450mg, 7 days a week) or in the case of severe turbo cancers up to 1 gram — for MEGADOSE 1,350mg-2,000mg/day — for prophylaxis one 150mg tablet once or twice per week

• Ivermectin (24mg, 7 days a week) or in the case of severe turbo cancers up to 1mg/kg/day — for MEGADOSE 120mg-200mg/day — for prophylaxis one 12mg tablet once or twice per week

• Hydroxychloroquine (10mg/kg/day 7 days a week) - for prophylaxis one 200mg tablet once or twice per week

• Doxycycline (100mg, 7 days a week for 30-60 days)

• ImmunX immune support which also greatly increases the bioavailability of both Fenbendazole and Hydroxychloroquine (2 capsules per day) — for prophylaxis 2 capsules per day

• Removing sugars and carbohydrates (cancer food) from your diet and replacing table sugar with a zero glycemic index, zero calorie, keto friendly rare sugar like AlluX

Do NOT comply.

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🇺🇸THE MASSIVE LABOR DAY 40% OFF SALE!🇺🇸 ends Tuesday, September 8th (midnight eastern time), 2026.

Upon adding products to your cart, please go to the cart icon at the top right corner of your browser page and click it, then choose the VIEW CART option whereby you will be redirected to a page where you can enter the code LABOR40 in the Use Coupon Code field.

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• Both Ivermectin and Fenbendazole must be taken with high fat meals to improve bioavailability

• Fenbendazole as per research studies is significantly more bioavailable when taken with a multivitamin or nutraceutical

• Fenbendazole is vastly superior to Mebendazole

Building on this protocol, in a recent research study titled, Hydroxychloroquine lowers dementia risk in humans, improves molecular signs of Alzheimer’s in mouse and cell models, the authors stated the following:

Taking hydroxychloroquine (HCQ) is linked to lower rates of Alzheimer’s disease and related dementias in people with rheumatoid arthritis, according to an international team of researchers led by NIA scientists. The study, published in Molecular Psychiatry, also included mouse and cell models to show that HCQ can improve early molecular signs of Alzheimer’s by reducing inflammation and enhancing the clearance of abnormal buildup of proteins that form amyloid plaques and neurofibrillary tangles. Because HCQ is already FDA-approved for other health conditions, these new study results could lay a strong foundation for clinical trials to test HCQ in older adults who are at high risk of developing dementia.

The authors concluded:

We recently nominated cytokine signaling through the Janus-kinase-signal transducer and activator of transcription (JAK/STAT) pathway as a potential AD drug target. As hydroxychloroquine (HCQ) has recently been shown to inactivate STAT3, we hypothesized that it may impact AD pathogenesis and risk. Among 109,124 rheumatoid arthritis patients from routine clinical care, HCQ initiation was associated with a lower risk of incident AD compared to methotrexate initiation across 4 alternative analyses schemes addressing specific types of biases including informative censoring, reverse causality, and outcome misclassification (hazard ratio [95% confidence interval] of 0.92 [0.83-1.00], 0.87 [0.81-0.93], 0.84 [0.76-0.93], and 0.87 [0.75-1.01]). We additionally show that HCQ exerts dose-dependent effects on late long-term potentiation (LTP) and rescues impaired hippocampal synaptic plasticity prior to significant accumulation of amyloid plaques and neurodegeneration in APP/PS1 mice. Additionally, HCQ treatment enhances microglial clearance of Aβ_1-42, lowers neuroinflammation, and reduces tau phosphorylation in cell culture-based phenotypic assays. Finally, we show that HCQ inactivates STAT3 in microglia, neurons, and astrocytes suggesting a plausible mechanism associated with its observed effects on AD pathogenesis. HCQ, a relatively safe and inexpensive drug in current use may be a promising disease-modifying AD treatment. This hypothesis merits testing through adequately powered clinical trials in at-risk individuals during preclinical stages of disease progression.

In a Nature article titled, Hydroxychloroquine lowers Alzheimer’s disease and related dementias risk and rescues molecular phenotypes related to Alzheimer’s disease, the authors showed an infographic for their study:

The Nature article concluded:

In summary, we have established that the commonly used RA drug, HCQ lowers AD risk in older individuals, and targets multiple pathogenic mechanisms in AD including synaptic dysfunction, neuroinflammation, Aβ clearance, and tau phosphorylation. Our results provide compelling evidence that this safe and inexpensive drug may be a promising disease-modifying treatment for AD. Confirmation of our findings in adequately powered clinical trials in at-risk individuals during preclinical stages of disease progression should be initiated in a timely manner.

The authors of the Nature study wrote a followup article titled, Hydroxychloroquine and Alzheimer’s disease, making some important clarifications:

Our paper, recently published in Molecular Psychiatry, suggests that hydroxychloroquine (HCQ), a relatively safe and inexpensive drug in current use, may be a promising disease-modifying Alzheimer’s disease (AD) treatment. The recent controversy around hydroxychloroquine’s use as a treatment for COVID-19 notwithstanding, the drug’s storied past and almost four centuries old history as a therapy for multiple diseases is a fascinating backdrop to our research.

Because Hydroxychloroquine stopped the gain-of-function (GOF) PSYOP-19 virus dead in its tracks such that there could never have been an “emergency” use authorization (EUA) granted by the captured FDA for their DEATHVAX™, and because wide administration of Hydroxychloroquine would have had positive side effects such as the significant reduction of Alzheimer’s and dementia in the populace, as well as prevention of curing of cancers…

…the powers that be had no choice but to smear and destroy Hydroxychloroquine, all while Dr. Fauci’s captured cadre of researchers deliberately designed flawed in vitro studies fraudulently demonstrating that Hydroxychloroquine would not be effective against their GOF plandemic (adding HCQ to low pH petri dishes approximating blood acidosis [cytokine storm phase post viral infection] in which case no compound works other than steroids), except that HCQ was around 100% effective against viral infections in real-world settings.

The researchers ended their op-ed with the following:

In summary, there is an urgent need to develop safe, effective, and easily accessible treatments for AD, which is a global public health challenge. Our research suggests that HCQ, an inexpensive, relatively safe and FDA-approved immune modulating drug in common use may benefit patients in early stages of AD by impacting multiple molecular pathways involved in the disease. These findings merit timely confirmation in adequately powered human clinical trials.

Hydroxychloroquine is also a powerful anti-inflammatory compound that only may be a treatment for Alzheimer’s Disease (AD) and cancer, but also autoimmune diseases like systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA), offering significant benefits in preventing flares, reducing organ damage, and improving survival rates.

Thus, the latest revised AD protocol:

Dementia & Alzheimer’s Disease Cure Protocol

• Fenbendazole 150mg every other day with dinner for 30 days, and repeat every 4 months

• Ivermectin 12mg every evening with dinner indefinitely

• Low dose lithium orotate 4.8mg capsule in the morning with breakfast and in the evening with dinner indefinitely

• Hydroxychloroquine 200mg every evening with dinner indefinitely (“HCQ-associated lowering of AD risk emerges after approximately 2 years of treatment”)

• ImmunX immune support 2 capsules in the morning with breakfast indefinitely (Quercetin is a critical ingredient in ImmunX, and as per research studies similar to Ivermectin it displayed capabilities against tauopathy by inhibiting the hyperphosphorylation of the tau protein, thus its anti-prion activity helps to reverse Alzheimer’s Disease)

• Removal of sugars and carbohydrates, and replacing table sugar with a zero glycemic index, zero calorie, keto friendly rare sugar like AlluX

• Creatine Monohydrate 4 x 500mg capsules every evening with dinner indefinitely

• Methyl B-12 1 x 1,000mcg daily on empty stomach (water-soluble vitamins are better absorbed without food interference [given that AD’s patients have been shown to have severe vitamin B-12 decencies])

• A high fat diet, with daily ingestion of organic pasture eggs, and other quality fats (brain food that also greatly increases Ivermectin and Fenbendazole bioavailability)

Which brings us to the previously published article on the fungal infection thesis causing AD:

Some researchers have suggested that neurodegenerative diseases like Alzheimer’s, Parkinson’s, and multiple sclerosis may have a microbial origin; thus, inexpensive repurposed drugs may be the cure.

A recent article by The Epoch Times posited that fungal infections may be the cause of neurodegenerative diseases.

A team of researchers at Baylor College of Medicine has discovered that when the brain is infected with a common fungus, it changes in ways similar to those seen in Alzheimer’s disease. The new research delves deeper into some of the molecular mechanisms behind that process.

The Study Findings

Using animal models, the research team discovered how the fungus, called Candida albicans (C. albicans), enters the brain, activates mechanisms for its clearance, and generates amyloid beta (Aβ)-like peptides—toxic protein fragments thought to be central to the development of Alzheimer’s disease.

The findings were published Oct. 10 in the journal Cell Reports.

Previous research has implicated fungi in the development of chronic neurodegenerative diseases like Alzheimer’s disease, but their mechanisms are not entirely understood.

We know that Candida thrives on sugars, so diets high in processed junk foods may very well be feeding the funguses that in turn destroy brains.

We also know that the inexpensive and repurposed drug Fenbendazole eradicates these funguses; for example, a research study entitled, The Anti-helminthic Compound Mebendazole Has Multiple Antifungal Effects against Cryptococcus neoformans stated the following:

Cryptococcus neoformans is the most lethal pathogen of the central nervous system. The gold standard treatment of cryptococcosis, a combination of amphotericin B with 5-fluorocytosine, involves broad toxicity, high costs, low efficacy, and limited worldwide availability. Although the need for new antifungals is clear, drug research and development (R&D) is costly and time-consuming. Thus, drug repurposing is an alternative to R&D and to the currently available tools for treating fungal diseases. Here we screened a collection of compounds approved for use in humans seeking for those with anti-cryptococcal activity. We found that benzimidazoles consist of a broad class of chemicals inhibiting C. neoformans growth. Mebendazole and fenbendazole were the most efficient antifungals showing in vitro fungicidal activity. Since previous studies showed that mebendazole reaches the brain in biologically active concentrations, this compound was selected for further studies. Mebendazole showed antifungal activity against phagocytized C. neoformans, affected cryptococcal biofilms profoundly and caused marked morphological alterations in C. neoformans, including reduction of capsular dimensions. Amphotericin B and mebendazole had additive anti-cryptococcal effects. Mebendazole was also active against the C. neoformans sibling species, C. gattii. To further characterize the effects of the drug a random C. gattii mutant library was screened and indicated that the antifungal activity of mebendazole requires previously unknown cryptococcal targets. Our results indicate that mebendazole is as a promising prototype for the future development of anti-cryptococcal drugs.

Thus, we may extrapolate that Fenbendazole, being a powerful antifungal, may quickly and permanently reverse these kinds of neurodegenerative diseases.

(Mebendazole is vastly inferior to Fenbendazole, and only exists because BigPharma awarded itself a bogus patent as a money grab while offering a relatively ineffectual substitute.)

And precisely because C. albicans has been shown to generate toxic protein fragments like amyloid beta (Aβ)-like peptides in the brain, Fenbendazole would be an especially strong candidate for potential therapeutic use in Alzheimer’s treatment.

Back to The Epoch Times article, which reinforces this notion of fungal-induced cognitive decline:

Humans and C. albicans have a complicated relationship, as most of the time, C. albicans is harmless and is simply a member of a healthy microbiota. However, it is one of the few fungal species that cause disease in humans and is responsible for infections that range from superficial infections of the mucosa and skin, like thrush, diaper rash, and vaginal yeast infections, to more serious infections like invasive candidiasis that can affect the blood, heart, brain, and bones.

Infections by C. albicans are particularly dangerous for those with compromised immune systems, like those with AIDS, or people undergoing immunosuppressive therapies for cancer and other conditions. This suppression of the body’s defenses is part of the reason why some people acquire C. albicans infections after taking antibiotics, as they decrease the beneficial bacteria in the gut, causing an imbalance and allowing C. albicans to thrive. C. Albicans can survive outside the body and have the ability to colonize every human organ and tissue. According to the Encyclopedia of Microbiology, it is the most common cause of systemic fungal infections.

Since so much of humanity is now suffering from (subclinical) VAIDS, infections by C. albicans will become far more prevalent, as will the associated cases of Modified mRNA “vaccine”-induced early onset dementia and Alzheimer’s.

In a January review published in Frontiers in Immunology, researchers examined the role of fungus in central nervous system autoimmune and neurodegenerative disorders. The review states that recently, increasing evidence has pointed to the role of peripheral fungus in triggering inflammation, immune response, and worsening of a range of non-infectious disorders of the central nervous system (CNS), including multiple sclerosis, Parkinson’s, and Alzheimer’s disease.

The review concluded that fungus can trigger inflammation via different mechanisms in the progression of CNS non-infectious diseases, suggesting that it is crucial for developing future therapeutic agents and strategies.

A 2015 study published in Scientific Reports states that several researchers have proposed the possibility that Alzheimer’s disease may have a microbial cause. The researchers found evidence that tissue from the central nervous system (which includes the brain and spinal cord) of patients with Alzheimer’s disease contains fungal cells. These fungal cells were found in different regions of the brain, including the external frontal cortex, cerebellar hemisphere, entorhinal cortex/hippocampus, and choroid plexus. These fungal materials were not present in the control individuals who did not have Alzheimer’s disease. The researchers identified several different species of fungus in their samples.

What is of particular note are the surges of both blood clots and immunocompromisation coinciding with the DEATHVAX™ rollout, and the consequent increases of fungal infection susceptibility contributing to ever more deadly outcomes:

Interestingly, the study authors noted that fungal infection was also found in the blood vessels, which could explain the vascular pathology that is often found in Alzheimer’s patients.

Once again, the confluence of “vaccine” adverse events is truly curious.

The findings provide intriguing evidence that these fungal infections are present in the central nervous systems of those with Alzheimer’s disease and not in healthy individuals who served as the controls.

Given that over time the slow kill bioweapon injections cause increasingly larger swaths of society to become unhealthy, unvaccinated healthy individuals will serve as the ultimate controls, especially for increasingly prevalent diseases such as dementia and Alzheimer’s.

Another Piece of the Puzzle

Dr. Corry and his colleagues have provided another piece to further understand the role fungus may play in the development of Alzheimer’s disease.

“This work potentially contributes an important new piece of the puzzle regarding the development of Alzheimer’s disease,” Corry said in a press release. “The current explanation for this condition is that it is mostly the result of the accumulation of toxic Aβ-like peptides in the brain that leads to neurodegeneration. The dominant thinking is that these peptides are produced endogenously [internally], our own brain proteases break down the amyloid precursor proteins generating the toxic Ab peptides.”

Due to their anti-prion activity, the other pieces of the therapeutic puzzle are Ivermectin and Quercetin (ImmunX has the perfect daily serving of Quercetin).

Ivermectin, another antiparasitic drug, was shown by Kawasaki et al. (2007) to have prevented the formation of the infectious form of the prion protein in prion-infected cells. Meanwhile, Quercetin, a flavonoid, extended the lifespan of prion-infected mice, highlighting its therapeutic potential against prion diseases.

Both compounds have also exhibited properties that modulate tauopathy, a characteristic of Alzheimer’s disease. Ivermectin inhibited tau hyperphosphorylation and even disaggregated tau fibrils. Quercetin, too, displayed capabilities against tauopathy by inhibiting the hyperphosphorylation of the tau protein.

The discovery of Fenbendazole, Ivermectin, Hydroxychloroquine, and Quercetin’s potential therapeutic properties underscores the importance of repurposing existing drugs in order to create highly accessible new treatment paradigms for neurodegenerative diseases.

Do NOT comply.

🇺🇸 THE MASSIVE LABOR DAY 40% OFF SALE! 🇺🇸 continues, so please use code LABOR40 to receive 40% off on all of the incredible lifesaving products like the newly released topical Ivermectin Cream, the Nobel Prize winning miracle compound Ivermectin, the no less miraculous Fenbendazole, Hydroxychloroquine, Doxycycline, the full spectrum organic CBD oil containing 5,000 milligrams of activated cannabinoids and hemp compounds CBD, CBN & CBG, the powerful immune support nutraceutical and spike support formula ImmunX, and the sugar craving reducing, blood sugar balancing and even anti-cancer allulose sugar substitute AlluX!

🇺🇸THE MASSIVE LABOR DAY 40% OFF SALE!🇺🇸 ends Tuesday, September 8th (midnight eastern time), 2026.

Upon adding products to your cart, please go to the cart icon at the top right corner of your browser page and click it, then choose the VIEW CART option whereby you will be redirected to a page where you can enter the code LABOR40 in the Use Coupon Code field.

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🔥 This from Rand Paul’s latest documents is a huge and shocking data point, worth further investigation.

It suggests that the CIA and Pfizer knew they were lying to the public on the very need for a Covid shot at all. By the time of release, according to their own math, shared only privately, we would already have achieved herd immunity.

On May 7, 2020, CIA Chief Operating Officer Andy Makridis led a briefing with Pfizer’s Scott Gottlieb. The CIA summary of the meeting: “On ‘herd immunity’ Dr. Gottlieb...believes nationally, the seroprevalence is about 20-25% which is insufficient for herd immunity at the R₀ (BRR) value of 3.”

Screenshot attached. In the same time frame, he was telling the public it was low around 8%. Even 3.5 months later, August 16, 2020, he was STILL claiming a low seroprevalence rate nationally. Screenshots attached.

What this means: both Gottlieb AND the CIA KNEW early on that endemicity would be obtained by the time of the shot release. They lied in public while telling the truth in private. https://paul.senate.gov/wp-content/uploads/2026/08/2026.08.29_Final-Hearing-Document-Release-Package.pdf

Source

The gain-of-function (GOF) viral release was always just meant to cull the most vulnerable in society in order to instill sufficient fear while providing the optics for optimal social engineering compliance with MK Ultra masks, panic pushed by the Mockingbird MSM quislings, etc. & etc. & etc. en route to the coordinated distribution of the far more devastating bioweapon payloads in their “free” gene altering eugenics injections.

The CIA just so happens to be one of the unconstitutional agencies that comprises the broader Intelligence-Industrial Complex (the 4th Branch of Government), with fellow war agencies like DoD, DARPA and the Pentagon owning most of these C19 “vaccine” patents; in other words, these injections as per their patent holders can only be classified as bonafide bioweapons, with the CIA being instrumental in helping to orchestrate the PSYOP-19 scamdemic, along with coordinating with the likes of Bill Gates, WEF, WHO, et al., and universities like Johns Hopkins for their EVENT 201 pandemic tabletop exercise just weeks before their “pandemic” scheme went live.

So when the CIA Chief Operating Officer Andy Makridis led a briefing with Pfizer's Scott Gottlieb all while the criminal FDA was issuing bogus “emergency” use authorization (EUA) on these deadly gene therapies that not only never received RCT with placebo-control trials, but were known to have never made it past any animal trials due to their extraordinarily dangerous outcomes…

…the CIA not only knew that endemicity would be achieved by the time of their “vaccine” release, but they also without a shadow of a doubt all knew that these injections would induce VAIDS, and trigger a tsunami of severe adverse events, all by design.

Of course, this unconstitutional spy agency by law cannot run any operations on domestic soil, but since this Constitutional Republic is now approaching banana republic status, with color of law and systemic grift representing some kind of pretend justice, the following should be painfully obvious to anyone paying a scintilla of attention:

Lest one forgets, the PSYOP-19 operation allowed the CIA and their radical Marxist politician assets to steal the 2020 elections under cover of this viral outbreak.

And now the CIA is expanding their takeover with the usual “private” sector cover and plausible deniability:

It’s CIA everything.

So, if the CIA was behind the PSYOP-19 plandemic…

…and the CIA was running all of the biolabs, not limited just to Wuhan…

…and the CIA is still running its MK-Ultra program on Americans…

…then it should come as little surprise that the CIA has for decades covered up the true nature of cancer, while suppressing cures that actually work so that their Medical-Industrial Complex partners-in-crime could generate windfall profits while torturing and murdering off patients with bogus “treatments” that they knew could never be optimal and were deliberately unviable…

…then it must also follow that the CIA does not want Americans to have access to inexpensive, truly safe and demonstrably effective repurposed compounds that would constitute the ‘holy grail’ cancer cure in plain sight that counters their ongoing cash cow VAIDS-induced turbo cancer epidemic, all while addressing Alzheimer’s, mood disorders, Parkinson’s, Lyme Disease, Alpha-Gal Syndrom from Lone Star Disease, myocarditis, Hashimoto’s Disease, shingles (herpes), arthritis, Multiple Sclerosis, diabetes, asthma, leukemia, Lupus, skin conditions, various other “incurable” ailments, “vaccine” shedding, seasonal flu and even the common cold:

The Ultimate Disease Cure & Prophylaxis Protocol

• Tocotrienol and Tocopherol forms (all 8) of Vitamin E (400-800mg per day, 7 days a week). A product called Gamma E by Life Extension or Perfect E are both great.

• Bio-Available Curcumin (600mg per day, 2 pills per day 7 days a week). A product called Theracurmin HP by Integrative Therapeutics is bioavailable.

• Vitamin D (62.5 mcg [2500 IU] seven days a week).

• CBD oil (1-2 droppers full [equal to 167 to 334 mg per day] under the tongue, 7 days a week) CBD-X: The most potent full spectrum organic CBD oil, with 5,000 milligrams of activated cannabinoids and hemp compounds CBD, CBN & CBG per serving.

• Fenbendazole (450mg, 7 days a week) or in the case of severe turbo cancers up to 1 gram — for MEGADOSE 1,350mg-2,000mg/day — for prophylaxis one 150mg tablet once or twice per week

• Ivermectin (24mg, 7 days a week) or in the case of severe turbo cancers up to 1mg/kg/day — for MEGADOSE 120mg-200mg/day — for prophylaxis one 12mg tablet once or twice per week

• Hydroxychloroquine (10mg/kg/day 7 days a week) - for prophylaxis one 200mg tablet once or twice per week

• Doxycycline (100mg, 7 days a week for 30-60 days)

• ImmunX immune support which also greatly increases the bioavailability of both Fenbendazole and Hydroxychloroquine (2 capsules per day) — for prophylaxis 2 capsules per day

• Removing sugars and carbohydrates (cancer food) from your diet and replacing table sugar with a zero glycemic index, zero calorie, keto friendly rare sugar like AlluX
  

Do NOT comply.

🇺🇸 THE MASSIVE LABOR DAY 40% OFF SALE! 🇺🇸 continues, so please use code LABOR40 to receive 40% off on all of the incredible lifesaving products like the newly released topical Ivermectin Cream, the Nobel Prize winning miracle compound Ivermectin, the no less miraculous Fenbendazole, Hydroxychloroquine, Doxycycline, the full spectrum organic CBD oil containing 5,000 milligrams of activated cannabinoids and hemp compounds CBD, CBN & CBG, the powerful immune support nutraceutical and spike support formula ImmunX, and the sugar craving reducing, blood sugar balancing and even anti-cancer allulose sugar substitute AlluX!

🇺🇸THE MASSIVE LABOR DAY 40% OFF SALE!🇺🇸 ends Sunday, September 8th (midnight eastern time), 2026.

Upon adding products to your cart, please go to the cart icon at the top right corner of your browser page and click it, then choose the VIEW CART option whereby you will be redirected to a page where you can enter the code LABOR40 in the Use Coupon Code field.

Only the RESOLVX HEALTH website offers all of the authentic products that this Substack promotes.

Please contact the company directly with any product questions: info@resolvx.health

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Code 2SGPET for 10% off ImmunX

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…and then the horrific Epstein files dropped…

…with the latest reveal further proving that this Mossad-backed child sex trafficking blackmail network, which is still fully operational and fully in control of Congress and various government agencies, is working with world leaders, installed useful idiot politicians and corporations to actively poison, infect, inject and ultimately depopulate the planet; to wit:

Absolutely wild timeline…

A Royal from Norway jokes with Epstein about humans no longer being able to have children

Epstein emails Bill Gates to plan ‘Pandemic Simulations’

A Pandemic ‘happens’ and Fauci demands that the World take Bill Gates’ vaccine

Fauci ignores the internal data of women having mass miscarriages after taking the ‘Covid Vaccine’ and deletes his emails

Source

Prior to the PSYOP-19 gene altering Modified mRNA slow kill bioweapon “vaccine,” there was another depopulation shot for an ailment that essentially does not even exist:

ALARMING WARNING: Dr. Carrie Madej Exposes the REAL Reason They Push the Tetanus "Vaccine" So Hard!

During her medical rotations in Detroit, Dr. Madej saw it firsthand:
Welfare patients who got the tetanus shot had MASSIVE fertility problems. Private-pay patients who refused? Extremely fertile.

Then she dug deeper:

"The World Health Organization and NIH have, since 1972, been developing the tetanus vaccine as an abortion or sterilization vaccine. They've been putting the pregnancy hormone (hCG) inside the tetanus vaccine... Every time you get it, it's a cumulative response. Your body will learn to attack an early pregnancy — so you wouldn't even know you got pregnant in the first place."

They've already used it in Latin America, Africa, and India. She believes they’ve been doing it here in the US too — while lying to doctors and the public for decades.

This is the SAME system now pushing other shots.

Wake up, protect your fertility, protect your future children.

REFUSE the tetanus "vaccine."

Source

Additionally:

Dr. Russell Blaylock: "The tetanus vaccine is one of the MOST RIDICULOUS vaccines ever."

Just got a cut or puncture wound? The ER is about to BULLY you into a TOXIC shot you don’t need.

Here’s what they won’t tell you:

The shot they push is NOT a simple tetanus vaccine — it’s the full DTaP combo loaded with:
• Aluminum (up to 0.625 mg — a known neurotoxin)
• Formaldehyde
• 2-phenoxyethanol + Triton X-100
• Milk protein (casein) & latex residues that can trigger anaphylaxis or CREATE new dairy/latex allergies

The tetanus toxoid inside has NEVER been properly safety-tested in a double-blind placebo-controlled trial. CDC admits it.

It’s grown on beef heart infusion with real risk of Mad Cow prion contamination.

Your actual chance of getting tetanus? 1 in 11 MILLION.

Spores live in manure, NOT rust. Clean the wound properly — oxygen kills them. 95% of the decline happened BEFORE any vaccine thanks to sanitation.

If you’re already exposed, the shot is useless — it takes 3-8 weeks for antibodies.

But high-dose Vitamin C (1–3g/day) cured 100% of cases in studies with ZERO deaths. Cheap. Safe. Ignored.

Why are we terrorized into this untested, poison-filled combo shot for a disease that’s basically extinct in clean countries?

Because fear sells.

Don’t fall for the rusty nail myth. Clean the wound. Monitor it. Refuse the jab.

Were you guilt-tripped into a “tetanus shot?” Were you ever told it was actually the full DTaP?

Source

It is all a deadly scam:

Which brings us to an article originally published on May 31, 2025 titled, Let’s Talk About Tetanus:

In this Substack’s ongoing series exposing that not a single vaccine is safe, effective, or necessary, not a single vaccine has an RCT with placebo-control, and that the entire vaccine program is simply an integral component of the greater NWO globopedo Great Depopulation program we bring you the deadly tetanus injection which is unrelentingly peddled as “$afe and Effective,” but in reality is exceedingly dangerous, sterilizing, and has absolutely zero efficacy.

Do you need a booster? Is the Tdap in pregnancy safe?

by Marcella Piper-Terry

Note: This article is about tetanus. There is no such thing as a “tetanus shot” anymore. The manufacturers stopped making the single tetanus shot in 2012. Since that time, getting a “tetanus shot” means getting either a DTaP or Tdap, depending on the person’s age, with DTaP being the option for infants and children up to age 7 years. Tdap is the version that is given to adults and children aged 7 and up. Tdap is also the one given to pregnant women. Because we cannot talk about the “tetanus shot” without discussing DTaP and Tdap, this article presents information about the childhood and adult vaccines, focusing more on the Tdap, particularly with regard to “tetanus boosters” and Tdap given to pregnant women.

“Help! My child cut herself on a piece of broken glass while washing dishes and she needs stitches. We are in the Emergency Room. They want to give her a tetanus shot. I’m scared. We don’t vaccinate, but the thought of tetanus is terrifying! What should I do???”

“Help! My husband was building a fence in the backyard of our suburban home, and he stepped on one of the nails. It went through his tennis shoe and left a puncture wound in his foot. It bled a lot, but we are concerned about infection, so we went to the doctor just to be sure he doesn’t need an antibiotic. They want to give him a tetanus shot. It was a new nail, purchased last week from Home Depot. Does he need a tetanus shot??”

And my personal favorite…

“My thirteen-year-old got stung by a bee. The pediatrician wants to give him a tetanus shot. Do bee stings cause tetanus???”

For the record…

(source)

Why in the world would a “tetanus shot” be given after a bee sting, you may ask? Because it is recommended. Apparently, that recommendation comes from an article published in 1879, which reported on a case of tetanus in a 34-year-old man who developed tetanus and who also had been stung by a bee “a couple of weeks prior.”

Well. That IS terrifying. Of course, we don’t know what John B. did during those weeks after the bee sting and prior to the onset of tetanus. Given that it was 1879 - prior to the invention of cars, and during a time when manure from horses was literally everywhere… and given the high probability that he did not have any antibiotic ointment or a band-aid to cover the sting, one might surmise that it was not the sting itself that caused the tetanus. It is likely that at some point following the sting, John B. was in the presence of horse manure, which he would have likely come into contact in if he walked anywhere or if he, himself owned a horse. If he set foot in the streets of any Northeastern city, he would have certainly gotten horse manure on his boots, and very likely on his clothing from the mixture of mud and manure that was everywhere in the streets of Boston, New York, and other major cities in the Northeastern United States at the time.

(source for photo above)

The scenarios quoted at the beginning of this article are illustrative of some of the many messages I have received through Facebook Messenger over the last fourteen years, since I started writing on FB about vaccines. Many people who do not vaccinate themselves or their children are terrified of tetanus. I have lost track of the number of times I have heard, “Tetanus is the ONE thing I’m really concerned about.” This statement often comes from friends who live on farms, who have horses and cows, or whose children participate in horseback riding as an activity. Because tetanus bacteria lives in the fecal matter of horses, cows, and other large mammals, the increased concern about tetanus in these environments is justified. However, if you live on a farm and you are concerned about tetanus, don’t go running to the doctor’s office asking for the vaccine just yet… Read on…

The many questions I have received about tetanus have spurred a few Facebook posts like this one:

Tetanus used to be a significant concern in the United States, back in the day before automobiles were invented and the streets were a stinky, sticky mixture of horse shit and mud. There are some really good write-ups on the history of tetanus and the vaccine. This one from Circle of Mamas is excellent. So is this one from National Vaccine Information Center. I encourage you to read both of these articles. After you finish here, please.

Did vaccines save us from tetanus?

As is the case with all “vaccine preventable” infections, those who benefit from the sale and uptake of vaccines try to take credit for the reduction in cases and deaths from tetanus. As this graph, from the Circle of Mamas article linked above shows, vaccines did not save us from tetanus.

The graph above is not an isolated scenario. As the two graphs below show, the decline in deaths from infectious diseases had little to do with vaccination, and a lot to do with improvements in sanitation (no more manure in the street, improvements in plumbing and clean water), and improvements in living conditions and nutrition. A really good resource for learning about this is the book, “Dissolving Illusions” by Dr. Suzanne Humphries and Roman Bystrianyk. If you want to take a quick look at the living conditions in American cities during the latter part of the 1800s, this is a great website. One quick perusal and you will easily see why infectious diseases were rampant in places like New York City and Boston prior to 1900s.

Note: Pertussis (whooping cough) and influenza are just two examples of infectious diseases for which the death rate had dropped more than 98% prior to the release of the vaccine that is said to have resulted in the reduction of deaths from said infection. If you want to learn more, please check this post - when you finish here, please.

When considering whether or not you should get a vaccine, you really should do a cost-benefit analysis that includes looking at the risk of serious outcomes, including death from the infection vs. the risks of serious outcomes, including death, from taking the vaccine.

What are your chances of dying from tetanus if you currently live in the United States?

“Since 1999, the number of deaths caused by tetanus in the United States has not exceeded 10 in a given year. This statistic shows the number of deaths caused by tetanus in the U.S. from 1990 to 2019.” (source)

As the above graph shows, the yearly average number of deaths from tetanus in the U.S. over the last twenty years is 7.5. In order to calculate your risk of death from tetanus, we need to know how many people live in the United States. According to the 2020 census data, that number is 329.5 million.

Dividing 329,500,000 (the number of people living in the U.S.) by 7.5 (the yearly average of deaths from tetanus) yields the following:

Your odds of dying from tetanus if you live in the United States are 1 in 43,933,333.333. Roughly, 1 in 44 million. Have you ever heard the ridiculous statement that serious vaccine injuries are 1 in a million? IF that were true (it’s not… ), that would mean your odds of serious injury from “tetanus” vaccination would be 44 times higher than your odds of dying from tetanus.

Tetanus is still a scary thing for some people. Part of the reason is because we have been told there is no cure for tetanus. Here is what the Mayo Clinic has to say:

Tetanus is a serious disease of the nervous system caused by a toxin-producing bacterium. The disease causes muscle contractions, particularly of your jaw and neck muscles. Tetanus is commonly known as lockjaw.

Severe complications of tetanus can be life-threatening. There’s no cure for tetanus. Treatment focuses on managing symptoms and complications until the effects of the tetanus toxin resolve.

Because of the widespread use of vaccines, cases of tetanus are rare in the United States and other parts of the developed world. The disease remains a threat to people who aren’t up to date on their vaccinations. It’s more common in developing countries. (source)

Is it true there is no cure for tetanus? No.

In this study, IV vitamin C (one gram per day) resulted in a 100% reduction in case-fatality rate in patients 12 years and under, and a 45% reduction in case-fatality rate in patients aged 13-30 years. The lower efficacy in older teens and adults is most likely because the dose was not high enough.

But my doctor says I need a booster every 10 years. Is this true? NO.

Here is the study.

Given that the World Health Organization (WHO) does not recommend tetanus boosters AT ALL for adults who have received the initial childhood series, why does the CDC continue to recommend boosters every ten years?

That’s right. The authors of the study suggest changing the adult schedule to recommend boosters every 30 years instead of every 10 years, as is currently recommended. They note that doing so would save an estimated $280 million per year and over $1 Billion in health costs over four years.

That recommendation was made in 2016. Eight years ago. Nothing has changed. And the reason is because the pharmaceutical industry and their minions in the government agencies that make the recommendations don’t care about the health (physical or financial) of America or our citizens. The $2 Billion that could have been saved went into their pockets.

What we know so far…

• If you live in the United States (or other developed nations) your risk of dying from tetanus is roughly 1 in 44 million.

• Vaccines had little to do with the reduction of death from tetanus. Improvements in sanitation, the invention of the automobile, and the resulting the shift away from horse poop in the streets had a lot more to do with the reduction in cases and deaths from tetanus.

• The pharmaceutical lobby and the U.S. government agencies who benefit financially from the sales of vaccines and who also make the recommendations for their use, via the child and adult schedules have chosen to ignore the recommendations of the World Health Organization (WHO) and scientific studies that show there is ZERO need for tetanus boosters every ten years, and in continuing to recommend boosters every ten years, they have increased their sales by an estimated $2 Billion over the last 8 years. For something that is completely unnecessary, and which is not without significant risk.

What ingredients of concern are found in tetanus-containing vaccines?

Here is where you can find the vaccine manufacturer’s inserts for all licensed vaccines in the United States. And below are links to the DTaP and Tdap vaccines, which is what you will receive if you consent to a “tetanus shot:”

DTaP Vaccines:

• Infanrix: 500 micrograms (mcg.) aluminum hydroxide, </= 100 mcg. formaldehyde, </= 100 mcg. Polysorbate 80 (TWEEN).

• DAPTACEL: 1.5 mg aluminum phosphate (333 mcg. of aluminum), ≤5 mcg formaldehyde, <50 ng residual glutaraldehyde and 3.3 mg (0.6% v/v) 2-phenoxyethanol.

Tdap Vaccines:

• Adacel: 1.5 mg aluminum phosphate (333 mcg. of aluminum), ≤5 mcg formaldehyde, <50 ng residual glutaraldehyde and 3.3 mg (0.6% v/v) 2-phenoxyethanol.

• Boostrix: 300 micrograms (mcg.) aluminum hydroxide, </= 100 mcg. formaldehyde, </= 100 mcg. Polysorbate 80 (TWEEN).

Occasionally, I will hear someone recommend getting the TD booster, which is Tetanus and Diphtheria, without the pertussis component. The TD vaccine information is listed below: