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Solving the Public Health Crisis

Interview with Etienne De Boetie2 from Art of Liberty Foundation

As Trump begins his presidency under the slogan Make America Healthy Again, how to reform public health is on everyone’s mind. Clearly it is public health policies that established the infrastructure that was weaponized against us during the dark days of Covid. One of Trump’s first actions as president was to get America out of the World Health Organization, which also stops the pandemic treaty, but we aren’t out of the woods yet. America is still a member of the United Nations, the other half of the WHO, and Trump recently met with Bill Gates at Mar-a-lago to discuss an Operation Warp Speed 2.0 using HIV vaccines. Let’s not forget that the bird flu has been declared a global emergency and mRNA cancer vaccines have been announced. There is a lot of discourse and many opinions floating around on how to solve the public health crisis.

I invited Etienne De la Boetie2 today to discuss a sample chapter from his soon to be released book Voluntarism-How the Only ISM Fair for Everyone Would Lead To Harmony, Prosperity, and Good Karma For All

Sample Chapter – Without “Government” What Would We Do About Healthcare?

Breaking Down What is Wrong in Healthcare

The cost of healthcare has been the main running point for anyone trying to reform healthcare for decades. HHS accounts for over 21% of the national budget and Medicare funding is frequently nominated for cost cutting. Etienne and it shows in the video, government run healthcare is expensive and getting the government involved only served to increase the cost.

To reduce cost of healthcare one must look at the products and services that are baked into healthcare. Doctors themselves pay massive amounts of money for medical school and it puts many of them in debt for life. Few are aware how much control medical licensing has over a doctor. As we saw during COVID, doctor’s that lose their license to practice are not able to pay off the debt in other fields in their lifetime. Many doctor’s couldn’t risk losing their license and being unemployable and bankrupt for life without them. To solve the problem of expensive healthcare, people often call for there to be a free healthcare system, or a socialized one. They want everyone to have access to healthcare, without the expensive price tag.

Part of that cost is in licensing of both medical schools and physicians through the AMA. These institutions are notorious for controlling how medicine can be practiced and the modalities of healing that are allowed to be taught. This is how protocols are created and physicians are trained not to question their indoctrination process. Following those protocols resulted in millions being killed in American hospitals by doctors during the dark days of COVID. If they didn’t, those doctors were de-licensed like Dr Paul Thomas, silenced, or fired. Leaving people who didn’t want to be murdered in a hospital by COVID protocols with no alternative. Doctors and health systems frequently follow protocols for all sorts of things, not just COVID. Doctors and hospitals can be sued if they don’t follow protocols. Etienne de la Boetie2 uses the term “defensive medicine”.

As a whistle blower who worked in the insurance industry, I feel compelled to inform people that built into every charge in healthcare is a fee for the required medical malpractice insurance that doctors are required to carry. This means that every time you pay a doctor for any kind of service, you are also paying their lawyers to represent them against you in court.

Tax Cuts

Etienne brings up an excellent point throughout his presentation how much of our money is paid in taxes and those taxes are the reason we don’t have enough money for healthcare. How much do Americans truly pay in taxes? Americans must work four months out of every year just to pay the IRS. Medicare taxes are included in that number. This healthcare tax is not optional, it is taken by your employer before you receive your cut. In a free market, if Medicare enacted a policy that you didn’t agree with such as forcing hospitals to vaccinate their staff as a condition of hire, or selling your medical record and genomic data data, people would have the right to stop payment.

Alternatives to Medical Insurance

https://odysee.com/@Voluntaryism:4e/Death_of_Lodge_Practice:5
  • Lodge Pole Practice
  • Crowd Health https://www.joincrowdhealth.com/
  • HSA Health Savings Accounts
  • Private Member Organization: constitutionally based business filing that keeps you and your business in the private sector where government regulations and medical licensing have no standing. https://www.pmasolutions.us/
  • Price Transparency for Surgeries: Surgery Center of Oklahoma

Where to Find Etienne de la Boetie 2

Speaking appearances & events | The Greater Reset | Art on the Rocks

Books | Voluntarism | Government Scam

Solving Covid – The Covid 19, Eugenics, and Vaccine/Drug Scam Timeline

Projects| The Thick Red Line


Natural Health & Healing Sources


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-Zowe Smith

From AIDS to COVID 1984

with David Rasnick

By Zowe Smith Published Jan 10th 2025

When rumors of false positive Covid tests began circulating, I became immediately suspicious. These Covid tests had been kept behind closed doors at the CDC, the only lab able to perform the testing. The moment the CDC released testing to be performed at outside labs and hospitals is the moment asymptomatic positives began to surge. Along with this change came the policy that every patient must be screened for Covid with a PCR test, regardless of presence of symptoms. Overnight, about 80% of our patient population were Covid patients because they had a positive test result on their chart.

What was going on with the Covid test? False positives mean the test did not work. Labs perform quality control regularly and calibrate their machines in order to maintain the integrity of test results. Their licencing depends on it. In addition, the lab can be sued for liable if they knowingly provide inaccurate results.

To answer the Covid-19 PCR test debacle, David Rasnick PhD is here to do a deep dive examining the idea that AIDS was a fraud on many levels and the same criminals that executed that scam also executed the Covid-19 scam. The evidence is undeniable when it is laid out so clearly.

Please see Part 1 for Dave’s qualifications and experience. A full interview complete with lots of supporting info can be found there.


Rumble link-Check out the Rumble Channel!

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This is a breakout collection of the slides David Rasnick presents in the video linked above. It does not include all the slides in the presentation. Shared with permission. Nobody can present this info the way Dave can, but feel free to dive in and share the info graphics if you like.

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Find David Rasnick’s work and learn more about AIDS, Covid & Cancer at Davidrasnick.com


Fauci & Gilead’s ‘Run Death is Near’ Scam was Recycled from 1984

Zowe

·

December 24, 2024

Fauci & Gilead's 'Run Death is Near' Scam was Recycled from 1984

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How Fauci is Giving Healthcare Workers AIDS

Zowe

·

December 31, 2024

How Fauci is Giving Healthcare Workers AIDS

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Covid PCR Fraud was Pulled from the HIV Playbook

Zowe

·

December 12, 2024

Covid PCR Fraud was Pulled from the HIV Playbook

This post will be a little different than my usual posts. It simply wouldn’t do if I wrote up one of my usual Substack articles that would get lost in the noise of reports of hundreds of current psy-ops. Regardless of the quality of the article, or how well the sources are linked, the impact wouldn’t be the same as bringing in someone who has been stud…

Read full story


PCR FRAUD

For a document you can use to use in court that shows beyond doubt that PCR is not a test, therefore it should not be used to diagnose anything. Evidence and arguments provided in the document. Go to

James Roguski

PCR Fraud

Share this link: PCRfraud.com…

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6 months ago · 438 likes · 142 comments · James Roguski


Thrill Kill Medical Cult .com

One of the best ways to support my work is to buy direct from the website. It’s the only place to get author signed copies too!

Available at multiple books distribution sites and Ebay.

T SHIRT SHOP (All designs now available in black except hoodies)

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-Zowe Smith

How Fauci is Giving Healthcare Workers AIDS

with HIV Protocol

by Zowe Smith Dec 31 2024

Healthcare Workers get PrEPped as LQBTQ Rainbow People

Chances are you have seen advertising for PrEP Drugs that are designed to be taken before a possible HIV exposure to protect against contracting HIV. One of the major brand names is Truvada, and it is primarily marketed to the gay community. PrEP stands for pre-exposure prophylaxis, and it is supposed to work a lot like a vaccine. The ad says you can still get and spread HIV while on the drug that is supposed to prevent people from getting or spreading HIV. Similar to an alleged ‘safe and effective’ Covid-19 shot that skipped safety steps during its warp speed development for your safety. A “therapy” that doesn’t meet the definition of a vaccine and was not tested to determine if it reduced transmission, only reduction in severity of illness.

Bet you haven’t heard that healthcare workers are also required to go on Truvada if they are exposed to a body fluid, and they have an open wound. It is part of an industry-wide HIV exposure protocol. The protocol for healthcare workers is called PEP, postexposure prophylaxis. It was widely talked about in every lab I ever worked in that the anti-viral drugs that healthcare workers are forced to go on come with severe side effects. There was a silent understanding that anyone who was prescribed the antivirals should avoid taking them at all cost. Many drugs cause terrible side effects. I wasn’t sure why the antiviral drugs in particular were so widely feared. Until now.

Here is the kicker. Truvada, PrEP, and PEP drugs are essentially AZT. The drug that Fauci pushed as the only HIV ‘treatment’. As David Rasnick explains in a recent interview, “the drugs cause the diseases they are supposed to prevent.” There is a list of 30-40 nucleoside analogue or antiretroviral drugs (abbreviated as ARVs) on the market. All of them cause AIDS and death. Peter Deusburg and other researchers discovered the prescribed dose of AZT was highly toxic, leading to lowered doses for all ARV drugs in the late 90s. Right about the time, the AIDS epidemic was considered to be over, according to the CDC. Under any other circumstances, a statement like that might seem like an exaggeration or a rare, yet possible, adverse event. Keep in mind, extreme measures have been taken to prevent the public from discovering just how toxic all nucleoside analogues like Truvada really are.

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Toxic Drugs Are the REAL Cause of AIDS

Side effects of ARVs start off seemingly mild enough but get more severe as the list goes on. It includes kidney failure, liver failure, bone loss leading to fractures, and various types of blood disorders. Blood disorders ultimately indicate an immune or nutritional deficiency. AIDS literally stands for acquired immune deficiency syndrome. It’s difficult to deny that ARV drugs can cause AIDS after performing a surface analysis of side effects alone.

Not satisfied that ARV drugs are the cause of AIDS yet? How about this fact? Researchers who were studying AZT in labs received a bottle with a warning label that read:

“Toxic by inhalation, in contact with skin, and if swallowed. Target organ(s): blood and bone marrow. If you feel unwell, seek medical advice (show the label where possible). Wear suitable protective clothing.”

Yet, patients who were told they were HIV positive and needed to take AZT to prevent the onset of AIDS received a prescription bottle (shown below) lacking any of the warning labels researchers would have received with the same drug. In fact, cancer doctors who prescribe AZT and other ARVs as chemo for life could go to jail for malpractice. Toxic effects to the blood, bone marrow, and contact with skin or, if swallowed, cannot be altered by placing the drug into a mislabeled bottle. How is it possible AZT isn’t harmful if prescribed, but it is considered deadly in a lab setting? How is it possible that prescribing AZT for cancer qualifies as malpractice, but prescribing it for HIV is considered a life-saving measure? The reality is that these are psychotic delusions that public health authorities desperately need you to believe. Either Wellcome, the NIH, and the FDA believe that prescription bottles magically change the chemical properties of a drug, or they are intentionally poisoning HIV victims for profit.

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Be PrEPared for the IRS

Kary Mullis. the inventor of the PCR process, spent a long time pondering how HIV was known to be the cause of AIDS without any scientific paper showing proof. He began questioning if something else was going on. How could AIDS be so deadly that a woman can raise a child before ever knowing she has it? That is an awfully long time to have a deadly disease and not know you have it. Yet, nobody can deny that HIV victims begin to experience symptoms of immune system failure after treatment begins. Note that patients are diagnosed as HIV positive with a test before any symptoms arise. Symptoms matching AIDS only appear after starting treatment.

Turns out, the toxic effects of ARV drugs are diagnosed and categorized as a condition called IRS or immune reconstitution (inflammatory) syndrome. ICD-10 code D89.3 and there are instructions to add a code for adverse effect of drug (i.e., poisoning). Referencing poison control for overdose or poisoning information on Truvada or any of its ingredients comes up empty. The professional monograph for healthcare providers also lacks typical information on drug overdose or poising instructions. It simply says if someone takes an extra dose of an ARV, the symptoms will be the same as normal side effects but a little worse than usual. Kind of suspicious right there if you ask me, but I am no doctor. Doctors and healthcare providers are trained to identify the toxic effects of ARV drugs as IRS, rather than drug related poisoning. The standard of care is to continue patients on ARV drugs to prevent the dreaded AIDS from returning or worsening, and manage the symptoms by throwing more drugs at it. Obviously, this approach will only serve to quicken the poor HIV victims’ demise.

IRS syndrome only occurs after treatment for HIV begins. There has never been an IRS patient that wasn’t on some kind of ARV drug. The tests and biomarkers used to diagnose HIV are different than the biomarkers used to identify IRS syndrome. I am currently unable to locate data on IRS biomarkers before and after treatment. There is an NIH published paper showing the biomarkers used to diagnose IRS syndrome could possibly be used to measure morbidity and mortality of HIV patients. This data further solidifies the hypothesis that the remedy for HIV actually causes the disease it is meant to treat.

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Merchants of Death Don’t Work for Free

Almost as if Gilead had studied from Wellcome’s AZT playbook, Gilead has a monopoly on Truvada which costs a pretty penny at almost $2,000 per month. Truvada is far from Gilead’s only ARV drug, the company states HIV drugs are one of the company’s best-selling products. Their other cash cow is Remdesivir.

AIDS activists are largely misinformed about Truvada. A group called PrEP4ALL is fighting Gilead to release the patent and lower the prices of Truvada. They believe the marketing slogans and fear campaigns perpetrated by the government and public health officials that antiretroviral drugs are life-saving medications. Unbeknownst to many AIDS activists, they are demanding a discount for willingly poisoning themselves. They might as well be asking for Kool aid from Jim Jones himself. Healthcare workers, on the other hand, are naively walking into a trap. It should also sicken you to realize that Gilead knows it makes deadly drugs that kill people. Their business model is to make that happen while turning a profit. Merchants of death don’t work for free.

There is a reason for the old saying “the remedy is worse than the disease”. They really are trying to kill us.

ThrillKillMedicalCult .com

One of the best ways to support my work is to buy direct from the website. It’s the only place to get author signed copies too!

Available at multiple books distributions sites and Ebay.

T SHIRT SHOP (All designs now available in black except hoodies)

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-Zowe Smith

Fauci & Gilead’s ‘Run Death is Near’ Scam was Recycled from 1984: Retrovir Vs Remdesivir

By Zowe Smith Dec 24, 2024

If you’ve come to this website titled “Thrill Kill Medical Cult,” chances are you’ve already ventured down a rabbit hole or two. Cheers to you for being hungry for knowledge and doing your own research! One of those rabbit holes may have informed you about a little drug called Zidovudine, more commonly known as AZT. If you are unfamiliar with the story of Fauci and the drug AZT, let’s go back in time to review the pertinent facts.

Scary Pandemic Announcements & Emergency Use Authorizations

AZT was originally a failed chemotherapy drug discovered by Jerome Horowitz in 1964. Thought useless due to its severe toxicity, the drug was tossed in the garbage bin and nearly forgotten. That is, until Mr. Fauci and Robert Gallo declared HIV a public health emergency in 1984. There were only about 3000 cases at the time. Hardly a drop in the bucket, but the decree of a public health emergency created mass panic regardless.

The number of cases of people living with HIV was so low during the early stages of the epidemic that many pharma companies were reluctant to develop a treatment product for fear of lack of return on investment. Fauci and Gallo continued to pump up the fear factor of a deadly epidemic, which sparked a race to find a drug that could fight the dreaded HIV nonetheless. A pharmaceutical company named Burrows Wellcome was first across the finish line with their drug AZT, brand name Retrovir.

At the time, it was the quickest drug approval in history, achieving approval within a span of just under two years. Most drugs take about 8–10 years to reach the FDA approval stage. AZT on the other hand, was fast tracked. On the surface, the study demonstrated that the AZT group had fewer deaths than the placebo group. Conditional approval was granted based on initial findings from an abbreviated study.

The ‘Benefits Outweigh the Risk’ Slogan

It was discovered shortly after approval that the participants and physicians in the double-blind study were unblinded early on. Clinical trials were a complete disaster, lacking any discernible scientific method, yet the study still demonstrated danger signals that were ignored. The benefit of providing potentially life-saving medications outweighed the risk of not having a treatment at all. It is the “benefits outweigh the risk” argument that was used in 1986 to pass the Vaccine Injury Compensation Program.

As the story goes, AZT became the only drug on the market for HIV “treatment”. Doctors prescribed AZT to anyone who came up positive for HIV, before symptoms ever appeared. Another word for that is asymptomatic spread. There was no evidence to support using AZT as a preventative, but if the drug worked to ‘treat’ AIDS once the disease was advanced, maybe it could stop HIV from progressing into AIDS. This proved to be a deadly mistake for many HIV/AIDS victims because it was the toxic effects of AZT that caused AIDS.

Any doubts Burrows Wellcome had over the profitability of AZT subsided as sales began to soar. They were concerned that the low number of AIDS cases would not translate into enough sales to support the product. For better or worse, their gamble to move forward with AZT paid off. The FDA’s lenient approval process for AZT assured Burrows Wellcome had a monopoly on the market. Not only that, but the drug was the most expensive drug ever marketed in its day.

Those who received a positive HIV test result were afraid they would die if they didn’t get treatment for HIV. The only treatment was Wellcome’s extremely expensive drug, AZT. HIV victims and their families applied pressure to Burrows Wellcome to reduce the cost. Reluctantly, Wellcome agreed to price reductions.

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Protocols That Authorize Medical Murder for Profit

If the tale of Fauci and AZT is giving you déjà vu, it is for a good reason. In the year 2020, another public health emergency was declared, by the WHO, this time and with Fauci’s assistance at the helm of the NIAID. Another public health emergency with a staggeringly low number of cases. Covid-19 was defined as a collection of common, non-specific symptoms and a test. People could allegedly be infected and spread it for up to 14 days. Remember they told us you can have HIV, and not know you have it, but still spread it to others? There’s that asymptomatic spread again. A fact that made Kary Mullis wonder how a disease could be so deadly (AIDS was declared to be 100% fatal in 1984) if someone could live long enough to raise a child before they even know they have the disease?

The NIH published a protocol for treating Covid-19 that involved exclusively using a drug called Remdesivir. Any potential alternative drugs were heavily discouraged or simply banned. Remdesivir was approved rapidly under EUA authorization, similar to how AZT was fast-tracked and approved without the usual required testing.

Remdesivir was originally developed for Ebola in 2017. It was not a forgotten toxic chemotherapy drug like AZT, but it was found to be deadly in 2018 long before its release. In 2019, Gilead worked with the DOD, WHO, CDC, and NIAID to fight coronaviruses with Remdesivir as quickly as possible. Soon, they had a patent and a new technology bonus built-in. The CARES Act also ensured bonuses for “new Covid treatments.” By that, it almost exclusively meant bonuses for Remdesivir. Financial incentives to use an exclusive ‘miracle’ drug against the scary Covid pandemic. Gilead had a product that couldn’t lose.

A monopoly was created on Remdesivir, just like Wellcome had on AZT. Sales from AZT helped Wellcome gain market share until it merged with Glaxo, and then Smith-Kline-Beecham to become Glaxo-Smith-Kline, the biggest drug company. Now known simply as GSK. Gilead is following in GSK’s footsteps while happily raking in billions in sales from Remdesivir (brand name Veklury).

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The Remedy is Worse than the Disease

The deadly effects of Remdesivir in combination with the application of ventilators caused patients to experience what the media told us was severe Covid-19 diseaseDr. Bryan Ardis does a fantastic job describing how Remdesivir causes kidney and other organ failure, which leads to pulmonary edema. Once the edema sets in, ventilator treatment is almost inevitable. Ventilation comes with another deadly concoction of drugs that shuts down the respiratory muscles and causes respiratory failure. It was a deadly protocol that few people escaped.

During both the Covid and AIDS public health emergencies, a pandemic of fear ensued, and the drugs meant to treat the dreaded disease, caused the very disease people were afraid of.

This is how a known toxic drug came to be prescribed to masses of asymptomatic victims that died from the treatment, not the disease.

“Anthony Fauci said in 1988 that AZT was the “only hope” for HIV/AIDS patients, when in reality it was their death sentence… Fool me once, Anthony Fauci; shame on you. Fool me twice; shame on me.” How AZT Killed My Brother

There is a reason for the old saying “the remedy is worse than the disease”. They really are trying to kill us.


ThrillKillMedicalCult.com

One of the best ways to support my work is to buy direct from the website. It’s the only place to get author signed copies too!

Available at multiple books distributions sites and Ebay.

T SHIRT SHOP (All designs now available in black except hoodies)

Media Channels| TELEGRAM CHANNEL | Twitter | GAB | Rumble

All the links

You were meant to be free, but you have to claim it!

-Zowe Smith

Covid PCR Fraud was Pulled from the HIV Playbook

Interview with David Rasnick

Zowe Dec 12, 2024

This post will be a little different than my usual posts. It simply wouldn’t do if I wrote up one of my usual Substack articles that would get lost in the noise of reports of hundreds of current psy-ops. Regardless of the quality of the article, or how well the sources are linked, the impact wouldn’t be the same as bringing in someone who has been studying the topic for decades to have an open discussion with us. So that is exactly what I did!

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Here with me today is David Rasnick PhD to help us investigate the accuracy of Covid-19 PCR tests and compare them to other methods of diagnostic testing for viruses. Dave was a long time friend of Kary Mullis, inventor of PCR, and several other colleagues whom were fierce critics of Fauci. He is an expert in clinical diagnostics, drug design, and AIDS. Founder of multiple biotech companies and formerly employed at Abbott labs. A name you will hear in my book, The Covid Code, for their HIV testing kits. He also participated as a member of the presidential AIDS advisory panel in South Africa. As you can see, David Rasnick is uniquely qualified to enlighten us about what was really going on with the Covid-19 PCR tests.

Spoiler alert, there are some incredibly Orwellian parallels to be made between the AIDS scam of the late eighties and early 90’s and the Covid-19 scamdemic (2020-2023). Most importantly, you will learn how the AZT scandal never stopped! It just went underground.

It is now my belief that the CDC initially controlled access to Covid-19 PCR testing while they worked on dialing in the fraudulent test before deploying it for mass use. Listen as Dave explains how titrating, or “tuning” test results has been done in this way since 1984.


For those of you who are eager to learn and want to do your own research, here is a list of source material mentioned in the interview.


Paper’s on COVID-19 Source Isolation

https://archive.org/details/1.-who-novel-coronavirus-2019-n-co-v

https://archive.org/details/2.-wu-1.7.2020-a-new-coronavirus-associated-with-human-respiratory-disease-in-china

https://archive.org/details/4.-cdc-12.1.20-cdc-2019-novel-coronavirus-2019-n-co-v-real-time-rt-pcr-diagnostic-panel

CDC Sequencing Instructions for Labs Performing Covid PCR Testing

https://web.archive.org/web/20220307234735/https://www.cms.gov/files/document/r10058cp.pdf

HIV Exposure Protocols

https://www.cdc.gov/hiv/workplace/healthcareworkers.html

https://www.cdc.gov/stophivtogether/library/prescribe-hiv-prevention/brochures/cdc-lsht-php-brochure-pep-faq.pdf

PEP and PrEP Drugs

https://www.hiv.gov/hiv-basics/hiv-prevention/using-hiv-medication-to-reduce-risk/post-exposure-prophylaxis

https://www.drugs.com/sfx/emtricitabine-side-effects.html

https://clinicalinfo.hiv.gov/en/drugs/emtricitabine-tenofovir-disoproxil-fumarate/patient

https://www.drugs.com/emtricitabine-tenofovir-disoproxil-fumarate.html#faq

https://pubmed.ncbi.nlm.nih.gov/7744255

https://www.catie.ca/azt-zidovudine-retrovir

IRS Syndrome (Post AZT)

https://www.aapc.com/codes/icd-10-codes/D89.3

https://www.icd10data.com/ICD10CM/Codes/D50-D89/D80-D89/D89-/D89.3

https://pmc.ncbi.nlm.nih.gov/articles/PMC3221202

Beginning of Gene Collection by PCR

https://archive.org/details/7.-butler-2007-short-tandem-repeat-typing-technologies-used-in-human-identity-testing

Metagenomics

https://archive.org/details/3.-bikel-2015-combining-metagenomics-metatranscriptomics-and-viromics

Mouse & Human Genome Comparison

https://archive.org/details/5.-waterston-2002-initial-sequencing-and-comparative-analysis-of-the-mouse-genome

https://archive.org/details/6.-human-genome-news-july-september-1996-8-1

Black box warning

https://www.ncbi.nlm.nih.gov/books/NBK538521

Peter Duesberg

https://www.duesberg.com

Luc Montagnier

FOIA’s on virus isolation

https://hive.blog/worldnews/@francesleader/email-exchange-with-uk-mhra-exposing-the-genomic-sequence-of-sarscov2

Christine Massey’s “germ” FOI Newsletter

“germ” FOIs – CDC, UNC Chapel Hill, NZ MBIE, Health Canada, PHAC, Maine CDC, Peterborough – no records!

Greetings and Best Wishes…

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2 years ago · 37 likes · 14 comments · Christine Massey FOIs


Medical Surveillance

Zowe

·

Jun 9

Medical Surveillance

Unedited Version

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James Roguski

PCR Fraud

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4 months ago · 438 likes · 142 comments · James Roguski

Where to find the movie VAXXED 3 Authorized to Kill


  1. WEBSITE:Get your books in print here! One of the best ways to support my work is to buy direct from the website and skip the middle man. Also available at multiple books distributions sites and Ebay.TELEGRAM CHANNELT SHIRT SHOP (All designs now available in black except hoodies)All the linksYou were meant to be free!-Zowe

Witness to Tragedy: ‘Huge’ Financial Incentives Led Hospitals to Use COVID Treatments That Killed Patients

Guest post by Michael Nevradakis, Ph.D. The Defender

This article was originally published by The Defender — Children’s Health Defense’s News & Views

Zowe Smith, who left her job as a medical coder in an Arizona hospital, joined “The Defender In-Depth” to discuss how the use of ventilators and remdesivir unnecessarily caused the deaths of COVID-19 patients admitted to hospitals.

by Michael Nevradakis, Ph.D. The Defender

September 19, 2024

Zowe Smith had a fairly mundane job. As a medical coder at an Arizona hospital, her job was to take information from patient records and “translate that into diagnosis and procedure codes.”

But when the COVID-19 shots and COVID-19 hospital protocols were introduced, Smith began to see things she’d never before seen in her career.

“We all believe that this is where people are supposed to go to get better … the hospital is supposed to help you,” Smith told “The Defender In-Depth” this week. “That’s not what was happening.”

Smith resigned and started speaking out about the suffering she saw recorded on patient medical records. She is the author of “The COVID Code: My Life in the Thrill Kill Medical Cult.” She also writes regularly on Substack.

Did DOJ Lawyers Commit Fraud in the Omnibus Autism Proceeding?

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Patients were ‘circling the drain’ soon after administration of COVID protocols

Smith said that medical coding, aside from being used for insurance purposes, is used to track the number of cases of diseases and illnesses regionally and nationwide.

Her job was to expose “the patterns of disease going on” in the population — and she said what she observed during the pandemic led her to begin questioning.

“Even when I was experiencing what I saw, it was almost unbelievable that this could even happen in a hospital,” said Smith, who first noticed abnormalities when the hospital started implementing COVID-19 protocols.

“I started noticing … patients trying to escape the hospital, like unplugging things, pulling out vent tubes and escaping … then I started to hear rumors about the ventilators and I knew that there was a bonus for [giving] remdesivir,” Smith said.

Smith said patients coming in with cold and flu symptoms were treated differently than they had been before the COVID-19 outbreak. “Before COVID, a cold, flu or pneumonia case, you would normally be home within three days, maybe a week, unless you had other major conditions.”

Before the pandemic, patients were rarely placed on ventilators. Smith said:

“Before the pandemic and the hospital protocols began, we did not connect patients to ventilators right away. It wasn’t until they were in dire straits and we had tried every other method that they would be put on a ventilator, and then they would be coming off those ventilators as soon as possible.”

But under the COVID-19 hospital protocols, patients “would be on the ventilators for 30 days or more sometimes, which was incredibly rare,” Smith said. “On top of that, they weren’t talking about disconnecting these patients from the ventilator, which should be something they’re talking about within 24 hours, because the longer you’re on, the less likely you are to come off the ventilator.”

Under the COVID-19 protocols, doctors “went straight to the ventilator” even if patient oxygen levels had not reached “the threshold where we would normally ventilate a person.”

Patients who were given remdesivir developed kidney failure within a few days. “I could see the lab values … they were getting worse almost immediately after the administration of remdesivir,” she said.

Smith described the pattern she observed: “Patient comes in, patient gets COVID diagnosis, patient [is] given a dose of remdesivir,” Smith said. “Pretty soon, they’re on vents. Pretty soon they have kidney failure and then they’re circling the drain and nothing that we could do would save them.”

Visits by loved ones were limited or prohibited due to pandemic restrictions and the hospital protocols — and this took a “horrific” toll on patients, Smith said.

According to Smith, patient records showed instances of “the police getting called to the hospitals” to eject “people that were trying to visit … dying loved ones or loved ones that were … being harmed by the hospital protocols.”

Smith said these patterns were evident to her as a medical coder. “Every note that happens between a nurse and a patient is documented. There’s social information that’s documented. There’s information from ambulance documentation that gets added to the medical record.”

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‘Huge incentive’ for ‘financially kneecapped’ hospitals to implement protocols

According to Smith, at the start of the pandemic, hospitals were placed under financial pressure — which later incentivized them to accept payments for implementing the COVID-19 hospital protocols.

“When the world was asked to lock down … hospitals were also issued mandates … that they needed to shut down their OR [operating rooms], which is their bread and butter. That’s where most of their money is made,” she said.

Hospitals also had to “increase their ICU [intensive care unit] bed capacity” and “reduce the number of patients in the ICU beds,” Smith said.

This “financially kneecapped hospitals for many months, from about March [2020] to May, when we were told we had to make room for this expected wave of COVID patients, which never came,” Smith said.

In the summer of 2020, after Congress passed the CARES Act (Coronavirus Aid, Relief, and Economic Security Act), the COVID-19 protocols “came down to us from the NIH” — the National Institutes of Health. The protocols prescribed the use of remdesivir and ventilators for suspected COVID-19 patients and financially incentivized struggling hospitals to use them.

Hospitals “got 20% for every single dose of remdesivir they gave to a patient … they got the bonus for it being a COVID patient to begin with. And then if the patient goes on a ventilator … they got the maximum payment,” she said.

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Hospitals hid vaccine injuries by not inquiring about vaccination status

Smith said medical records also contained evidence of patient injuries following administration of the COVID-19 vaccines.

“I began seeing some incredibly crazy cases,” Smith said. “I began to notice more cases … of near-instant death, like within an hour of multi-organ failure. Massive inflammation, brain death, things that we had never, ever seen before. In my 11 years of medical coding, I had never seen a case like that.”

She added:

“Most of those patients that had sepsis and the massive, whole-body inflammation did not make it. There were a lot of cases of seizures that were uncontrollable … and then people started to arrive with brain inflammation, encephalitis … some of them suffering from stroke-like symptoms. All of a sudden, massive blood clots coming in. And these were in young people. These were not elderly people with comorbidities.”

Yet, according to Smith, hospitals would not inquire about patients’ vaccination status, making it impossible to diagnose these conditions as vaccine injuries. “They weren’t asking the right questions [and] weren’t writing it in the medical record.”

Smith said she felt the need to turn her experience “into something positive.”

“Maybe I can take this information and put it out there so that people can be warned and they can know what’s going on,” Smith said. “To me, it’s about saving lives and it’s about helping us figure out what happened.”

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Michael Nevradakis, Ph.D., based in Athens, Greece, is a senior reporter for The Defender and part of the rotation of hosts for CHD.TV’s “Good Morning CHD.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

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Medical Surveillance

Part 1: From Contact Tracing to Gene bank AI “Ecosystem”

Medical Surveillance

Part 1: From Contact Tracing to Gene bank AI “Ecosystem”

JUN 13, 2024

Unedited Version

Originally Posted on The Last American Vagabond Substack on May 31, 2024

For more info and news go to The Last American Vagabond website

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BIG TECH BROUGHT IN FOR CONTACT TRACING

You may recall, early in the scamdemic, all the rage was about contact tracing. Public health officials advised Covid-19 could be spread by people who didn’t have symptoms for up to 14 days. Anyone who had been within six feet could be contaminated and unaware. Hospitals began questioning patients about their contacts. For the first time, personal information and that of their contacts, with was recorded.

This was not normal practice for other infectious diseases. It was normal to ask patients who had HIV about their partners. To my knowledge, it was up to the individual to tell those partners. Their contacts personal information did not become part of the record. The HIV patient’s data would then be de-identified and sent to a CDC database for disease surveillance purposes.

Social workers were brought in to help collect data for Covid-19 contact tracing. It was a tedious task that would not be sustainable without digital assistance. As early as April 2020, contact tracing had been outsourced to big tech. Smartphone apps for contact tracing were stealthily released through a regular update. Apple and Google claimed it was strictly an opt-in program. Anyone who updated their phone was passively being tracked via Bluetooth.  The only difference was that people who chose to participate got notifications when they were within six feet of a Covid-19 case.

BURNING THE FIREWALLS TO VIOLATE YOUR PRIVACY

Collecting the medical record data was sure to go through the American Hospital Information Management Association (AHIMA). They are responsible for licensing medical coders and other health information professionals. It is the responsibility of AHIMA to manage contact tracing data submissions. It also falls on AHIMA to regulate Covid-19 data submissions to the CDC. 

In their journal, I learned a disease registry for Covid-19 was being created through a partnership between labcorps and CIOX. Labcorps was one of the first public labs to roll out Covid-19 PCR testing. It was a perfect match, with Lapcorps providing access to test results combined with COIX’s data integration software

Covid-19 coalition was formed with the stated purpose of sharing and leveraging real-time data. When I put together the members of the Covid-19 registry and the coalition, I began to see how alarmingly public our private medical data has become. Some members of the coalition overlapped those of the registry; Amazon, google, and Microsoft. Some members like Palantir, MITRE and In-Q-Tel clearly represented the interests of government intelligence agencies.

When I became aware of this in early 2020, I was not the only one concerned with the massive amount of data being collected on people without their knowledge. Some parts of HIPAA, the law that is supposed to protect patient privacy, were waived to permit information sharing. More concerning still, this information appeared to be shared with big tech and government intelligence agencies. Instead of calming my fears about private medical data being shared, AHIMA was adding fuel to the fire.

I was unaware there was a program that required hospitals to send patient data to HHS at scheduled intervals. It was part of the HHS protect system. That kind of data transmission was above my pay grade. I was occasionally clued in if the transmission failed. I would overhear grumblings about how the hospital wouldn’t get paid if tech support was unable to fix it in time. I didn’t understand Medicare could reduce payments if hospitals failed to send the required information. The HHS protect system replaced The National Health Safety Network. It is the program Medicare exploits to tie funding to healthcare staff vaccination compliance.

AI IN ELECTRONIC MEDICAL RECORD SOFTWARE

It was shocking, to learn the 3M program I used as a medical coder, had AI built in. How did I not know this? The program had a feature called computer assisted coding. It used natural language processing to analyze records and predict ICD-10 codes. My job as a 3M trainer was to teach coders how to correct the auto-predicted codes. The more coders fixed errors, the machine learning feature would improve code predictions. The big wigs told coders the program was a tool to improve efficiency. In fact, it has been slowly taking over coding jobs as its usefulness improves.

The other program that dominates the electronic health record market in the United States is EPIC. Many hospitals use this program as their core electronic health record system. I learned during the scamdemic that EPIC has multiple AI features built-in as well.

The latest development in healthcare data integration is adding an AI listening feature to generate notes. 3M partnered with Amazon, a member of the Covid-19 information sharing coalition, on the project. The AI listening feature will be integrated directly into 3M. The program will listen to the whole conversation, and doctors will only have to approve the AI-generated note. This is a step ahead of EPICs dictation software, which operates a lot like talk to text on a smartphone. Physicians can also draft templates in EPIC and edit the variables. Either way, the downside is the doctor has to devote additional time generating the notes. EPIC is getting on board to solve this by integrating AI listening features into its software as well. The privacy concern with that is every computer in the hospital is always listening. This effectively kills any facade of privacy in healthcare.

PALANTIRS TENTACLES IN HEALTHCARE DATA

Palantir has a heavy hand in merging AI with electronic healthcare records or EHR programs. Palantir was contracted by the CDC to build a contact tracing app. For Operation Warp Speed, Palantir provided an artificial intelligence program called Tiberius. It was supposed to monitor the ICU bed capacity and ventilator availability. It layers 225 databases across the public and private sector and places them into one “ecosystem”. Tiberius can target ethnic groups based on risk behavior and location.  It doesn’t just map data, it can predict behavior. Palantir was a member of the Covid-19 registry and information sharing coalition.  Palantir also provided the AI platform used by HHS protect to distribute Remdesivir, the deadly drug that causes kidney failure. Not only that, Tiberius was also used to identify patients for vaccine clinical trials.

The CDC commissioned their contact tracing app with Palantir. It was later revealed contact tracing data was collected on Americans without their knowledge and used to give them an infection risk score. The CDC and Department of Homeland Security also purchased cell phone data to monitor lock down compliance, among other reasons.

Palantirs desire for data surveillance shouldn’t be a surprise, as the company was born from a failed CIA program called Total Information Awareness that was privatized. A look at Palantirs partnership with DARPA, In-Q-Tel, and the CIA confirms their roots in intelligence.

I found it disturbing that the other members of Palantir were software companies that developed the programs that were used in electronic record management and medical coding. They were EPIC, 3M, Optum, Allscripts, and McKesson. Every hospital system I worked for used at least one of those medical record systems. In order for these companies to work with Palantir, contracts are required that permit information sharing. An insider who formerly worked at the software development level at 3M, explains the information sharing that happens “is far more than you know”. 

THE PUBLIC-PRIVATE PARTNERSHIP VIRUS

The Covid-19 registry has been disbanded since HHS declared the end of Covid on May 11, 2023. Since then, all the links and references I saved lead nowhere. Registry members were agencies like the National Cancer Institute, NIH, NIAID, National Academies of Science, and Research Alliance Group. Not surprisingly, the Covid-19 vaccine manufacturers were members. The tech companies building the infrastructure were Amazon, Palantir, Google Cloud Services, and Microsoft Azure. Government and intelligence agencies were also noted as members. Any mention of DARPA, the CIA, or the Chinese governments involvement, has vanished without a trace.

As often happens, the Covid-19 registry database was absorbed into a private company. CIOX was acquired by Datavant. The Covid-19 registry has been integrated in Datavants real-world data AI ecosystem. There are over 500 partners that continually feed data into the ecosystem which can be used by all partners. Private patient information is de-identified in the ecosystem. Government agencies are allowed to see individually identifiable data, however, because they are exempt from privacy laws.

Healthcare systems partnered with China for Covid-19 research purposes during the pandemic. This granted them access to American healthcare data. The most valuable data is our DNA. As Karen Kingston (and Derrick Broze) points out, the Chinese government acquired Americans DNA under the guise of Covid-19 PCR testing.

BGI is China’s leading genomic company. They have been busy building a gene bank for a very long time. It started out for the human genome project. Like Datavant, BGI partnered with American tech companies to build the gene bank. Their goal is to be able to identify how individuals respond to viruses and vaccines. During the pandemic, BGI sold American providers, like labcorps, Covid-19 PCR test kits. Perhaps that is why the CDC required labs performing Covid-19 PCR tests to send genomic sequences to them. Labs were further instructed to upload the genomic data to public gene banks GISAID and NCBI. This is how our genetic data has been collected and uploaded into a public gene bank without our knowledge and how that information is shared with China.

MEDICAL SURVEILLANCE GOES UNDER THE SKIN

During the pandemic, the CEO of the hospital I worked for announced that city wastewater treatment plants would be equipped with Covid-19 PCR testing technology. It was proudly proclaimed as a way to predict pandemic outbreaks and monitor Covid in real time. As author Whitney Webb puts it, “under the guise of fighting Covid-19 [the medical industrial complex] increasingly seeks to monitor what is going into, out of, and happening within our very bodies.”. 

I had to agree, it seemed all the tracking and predictive AI programs were leading into dangerous medical pre-crime territory. Private medical data is being shared with international government and military agencies. DNA is being collected from the public to create a gene bank without their knowledge. The information is used by governments and intelligence agencies to predict behavior and target ethnic groups with countermeasures like Remdesivir and vaccines. What could go wrong?

In part two of “Medical Surveillance” we will take a look at how the same AI software was used to develop a vaccine passport system. You will also discover how vaccine status is being tracked via the ICD-10 codes. Stay tuned because where this all leads is more explosive than medical pre-crime.


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ICD-10 — The Code of the Medical Cult

My Life in the Thrill Kill Medical Cult with Zowe Smith

ICD-10 — The Code of the Medical Cult

My Life in the Thrill Kill Medical Cult with Zowe Smith

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The Deathwatch of 2020

We are all on deathwatch now.

Deathwatch: (noun) A vigil kept beside a dead or dying person. – Dictionary.com

We are all on deathwatch now.

It began slowly. In January 2020, there were rumors of a new disease, a killer, circulating in Italy, Wuhan, China, and soon in a couple of cruise ships.

Then, the first predictive modeling came out, projecting 2.2 million deaths in the US and 510,000 in the UK. That predictive computer model turned out to be quite wrong, but it was enough in March 2020 to lockdown the United States and most of the rest of the world.

There was a deathwatch in March through most of 2020. We all held our breath those first few months and watched with some confusion and cautious relief as the COVID deaths failed to match the modeling, but we were still under all the repressive pandemic measures.

Behind the scenes, there was another kind of deathwatch in hospitals. People who were robust and youthful were dying unexpectedly. Our guest, Zowe Smith, was one of the early medical personnel who made notes and privately questioned what she was seeing.

In her unique position as a senior medical coder with a large hospital, Zowe had access to all the data streams. Her responsibility was to take the patient information collected in the hospital for each patient and send billings to the patient’s insurance company for payment. She saw patient data, diagnoses, progression of care, the evolution of the patient’s condition, and the ultimate resolution, either through discharge or because of death.

And data was just not adding up for Zowe. Procedures, patient care, treatment protocols, drug administration, and more were being changed in unusual ways. Most alarmingly, patients were dying in larger numbers after being on ventilators for weeks or more and after being prescribed Remdesivir.

When Operation Warp Speed rolled out the COVID-19 “vaccines” in January 2021 to first responders and other early recipients, Zowe saw further changes. Suddenly, different kinds of deaths began to occur–massive blood clots and other blood abnormalities chief among them.

From her unique insider perspective, Zowe offers us a chilling hour of detail on how patients died during the year of COVID and how they died when the “vaccines” rolled out. She provides a vivid description of the intentional blindness of bureaucracy in the face of a genuine epidemic of iatrogenic, doctor-caused death that continues to this day.


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The Thrill Kill Medical Cult Exposed on Rebunked.News

Check out my recent interview on Rebunked. Scott was one of the freedom fighters in Oregon during lock downs, masking, and vaccine roll out. The podcast that gave rise to Rebunked, Truthzilla was the first one I went on to expose the truth! Scott was one of the hosts. It’s been a wild ride exposing the truth all these years. I’m grateful to be back, still exposing medical murder for profit and surveillance in healthcare. – 

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Click here to watch the livestream tonight at 6:30pm ET on Rumble

Joining me this evening is Zowe Smith, medical coder whistleblower and author of the upcoming book “My Life In The Thrill Kill Medical Cult”. Rebunked/Truthzilla broke Zowe’s story back in 2021 and it is cool to see her finally breaking into the mainstream, having just appeared on The Alex Jones Show. Let’s dive in!


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