The Toll of the Covid Jabs

74% of ALL Deaths ‘Directly’ Linked to Covid Shots, Autopsy Data Shows

A damning new study has revealed that autopsy data shows Covid mRNA shots have overwhelmingly contributed to all-cause deaths around the world.

The bombshell study found that Covid shots are “directly” linked to a staggering 73.9% of all deaths.

The research team behind the study was made up of some of America’s leading oncologists, cardiologists, doctors, and scientists, including:

  • Nicolas Hulscher
  • Paul E. Alexander
  • Richard Amerling
  • Heather Gessling
  • Roger Hodkinson
  • William Makis
  • Harvey A. Risch
  • Mark Trozzi
  • Peter A. McCullough

The study found that 73.9% of all deaths were “directly due to or significantly contributed to” by Covid mRNA injections.

The autopsy data exposes a direct link “between COVID-19 vaccination and death,” the researchers note in their study’s paper.

In the “Background” section of the study’s paper, the researchers explain:

“The rapid development of COVID-19 vaccines, combined with a high number of adverse event reports, has led to concerns over possible mechanisms of injury including systemic lipid nanoparticle (LNP) and mRNA distribution, Spike protein-associated tissue damage, thrombogenicity, immune system dysfunction, and carcinogenicity.

“The aim of this systematic review is to investigate possible causal links between COVID-19 vaccine administration and death using autopsies and post-mortem analysis.”

In the “Methods” section, they note:

“We searched PubMed and ScienceDirect for all published autopsy and necropsy reports relating to COVID-19 vaccination up until May 18th, 2023.

“All autopsy and necropsy studies that included COVID-19 vaccination as an antecedent exposure were included.

“Because the state of knowledge has advanced since the time of the original publications, three physicians independently reviewed each case and adjudicated whether or not COVID-19 vaccination was the direct cause or contributed significantly to death.”

The research team initially identified 678 studies.

After screening for our inclusion criteria, the researchers included 44 papers for the study that contained 325 autopsy cases and one necropsy case.

The mean average age of death was 70.4 years.

The most implicated organ system among cases was the cardiovascular (49%), followed by hematological (17%), respiratory (11%), and multiple organ systems (7%).

Three or more organ systems were affected in 21 cases.

The mean time from vaccination to death was 14.3 days.

Most deaths occurred within a week from last vaccine administration.

A total of 240 deaths (73.9%) were independently adjudicated as directly due to or significantly contributed to by COVID-19 vaccination.

Among those directly linked to Covid shots, the primary causes of death include:

  • Sudden cardiac death (35%)
  • Pulmonary embolism (12.5%)
  • Myocardial infarction (12%)
  • VITT (7.9%)
  • Myocarditis (7.1%)
  • Multisystem inflammatory syndrome (4.6%)
  • Cerebral hemorrhage (3.8%).

In the “Conclusions” section of the paper, the authors write:

“The consistency seen among cases in this review with known COVID-19 vaccine mechanisms of injury and death, coupled with autopsy confirmation by physician adjudication, suggests there is a high likelihood of a causal link between COVID-19 vaccines and death.

“Further urgent investigation is required for the purpose of clarifying our findings.”

The researchers warn that findings “indicate the urgent need to elucidate the pathophysiologic mechanisms of death with the goal of risk stratification and avoidance of death for the large numbers of individuals who have taken or will receive one or more COVID-19 vaccines in the future.”

The study comes amid a growing body of evidence linking the Covid mRNA injections to multiple deadly health conditions and related sudden deaths.

As Slay News recently reported, another bombshell new global study of 2.7 billion people has just determined that COVID-19 did not cause any excess deaths during or after the pandemic, despite widespread claims to the contrary from health agencies around the world.

However, the same explosive study has revealed that Covid mRNA shots, which were supposedly unleashed on the public to tackle the virus, have caused millions of excess deaths globally.

The study’s comprehensive 521-page report contains hundreds of figures and a detailed examination of excess all-cause mortality during the years 2020 to 2023 in 125 countries.

The dataset analysed by the researchers comprises approximately 2.7 billion people which is about 35% of the world’s population.

The researchers calculated that the global death toll associated with Covid mRNA shots, up to 30 December 2022, was 16.9 million people.

from:    https://slaynews.com/news/74-all-deaths-directly-linked-covid-shots-autopsy-data-shows/

List of Studies vis-a-vis VACCINE INJURIES

THIS IS JUST A VERY GREATLY ABBREVIATED LIST OF VACCINE INJURIES COMPILED BY K.C.  SHE HAS LISTS AND LISTS OF ARTICLES AND STUDIES TO BACKUP HER WORK.

GO TO THE LINK TO PERUSE THEM ALL:  https://ladycasey.substack.com/p/scientific-studies-on-vaccine-injuries?utm_source=substack&utm_campaign=post_embed&utm_medium=email

Scientific Studies on Vaccine Injuries

You want science? Here’s your f*cking science.

This post mainly consists of scientific studies (both peer reviewed and preprints), systematic reviews, case studies (a few key ones of the thousands out there), and other medical journal articles that support the assertions in my Vaccine Injury post from November 2022. I began bookmarking these studies in late 2021, but since I’ve surely missed some, this is not a comprehensive list. It is, however, significant enough to utterly debunk the “safe and effective” propaganda of the past three years. (I will continue adding to this list indefinitely, so please check back on occasion for the most recent scientific discoveries about C19 vaccine injuries.)

I’m not a scientific researcher, data analyst, or medical professional. Neither are most of my readers. However I, and presumably they/you, are fully intellectually capable of reading and understanding the discussions and conclusions in most of the studies listed below. For those of you who prefer to skim, in most cases, after each link below, I include a short (2-3 sentence) summary of the study’s conclusions.

Some of the studies below are followed by a supporting article explaining its findings in layman’s terms. All such articles are written by experts in their field, including scientific researchers, professors, data analysts, PhDs, MDs and other medical professionals. (Some accompanying articles are under a paywall, for which I apologize, however I’m happy to email my readers free versions of any linked articles upon request.)

Lastly, please take note that much of the pro-jab jargon used in these studies is required to survive peer review. Journals are beholden to (funded and captured by) the pharmaceutical industry. Researchers have stated outright that they cannot get published on this topic without the inclusion of pro-vaccine rhetoric in their studies.

Please use this post as a resource to backup your own arguments with uninformed acquaintances who continue to believe and perpetuate the false government/Pharma narrative that the C19 “vaccines” are safe. They are not, and the following evidence couldn’t be more clear about that.

General Adverse Events

  • Serious Adverse Events of Special Interest Following mRNA Vaccination in Randomized Trials
    https://www.sciencedirect.com/science/article/pii/S0264410X22010283
    (Peter Doshi—senior editor of the BMJ—study concluding that Covid vaccines were associated with an excess risk of serious adverse events of special interest of 12.5 per 10,000 vaccinated. And that the excess risk of serious adverse events of special interest surpassed the risk reduction for COVID-19 hospitalization. Explanatory articles herehere, and here.)
  • COVID-19 Modified mRNA “Vaccines” Part 1: Lessons Learned from Clinical Trials, Mass Vaccination, and the Bio-Pharmaceutical Complex
    https://www.ijvtpr.com/index.php/IJVTPR/article/view/101
    (“The usual safety testing protocols and toxicology requirements were bypassed. Many key trial findings were either misreported or omitted entirely from published trial reports. By implication, the secondary estimates of excess morbidity and mortality in both trials must be deemed underestimates. Rigorous re-analyses of trial data and post-marketing surveillance studies indicate a substantial degree of modmRNA-related harms than was initially reported. Confidential Pfizer documents had revealed 1.6 million adverse events by August 2022. A third were serious injuries to cardiovascular, neurological, thrombotic, immunological, and reproductive systems, along with an alarming increase in cancers. Moreover, well-designed studies have shown that repeated modmRNA injections cause immune dysfunction, thereby potentially contributing to heightened susceptibility to SARS-CoV-2 infections and increased risks of COVID-19. This paper also discusses the insidious influence of the Bio-Pharmaceutical Complex, a closely coordinated collaboration between public health organizations, pharmaceutical companies, and regulatory agencies.” Read the original paper here and explanation of its highly suspect & unethical redaction here.)
  • Potential health risks of mRNA-based vaccine therapy: A hypothesis
    https://www.sciencedirect.com/science/article/pii/S0306987723000117
    (“If our hypothesis were to be confirmed, the implications for public health would be staggering and appalling in the context of the mass-scale COVID-19 vaccination already taking place, particularly if the nms-mRNA enters brain, bone marrow, and – if already present in the vaccinee – cancerous or pre-cancerous cells, or if the vaccine is administered to females early in their pregnancy and the nms-mRNA transfects embryonic cells.”)
  • ‘Spikeopathy’: COVID-19 Spike Protein Is Pathogenic, from Both Virus and Vaccine mRNA
    https://www.mdpi.com/2227-9059/11/8/2287
    (“This paper reviews autoimmune, cardiovascular, neurological, potential oncological effects, and autopsy evidence for spikeopathy.” Also, ” Treatment modalities for ‘spikeopathy’-related pathology in many organ systems, require urgent research and provision to millions of sufferers of long-term COVID-19 vaccine injuries. We also advocate for the suspension of gene-based COVID-19 vaccines and lipid-nanoparticle carrier matrices, and other vaccines based on mRNA or viral-vector DNA technology.” Comprehensive explanatory article here.)
  • The Novelty of mRNA Viral Vaccines and Potential Harms: A Scoping Review
    https://www.mdpi.com/2571-8800/6/2/17
    (The COVID-19 vaccines are known to be unsafe for several reasons: 1) the Wuhan Spike protein damages cells, tissues, organs, and causes blood clotting, 2) the lipid nanoparticles may have toxicity from the PEG or polysorbate 80 or from syncytia formation, 3) the mRNA appears to be resistant to ribonucleases and is not broken down in the body. As some point the mRNA or fragments could interfere with gene function or alter other microRNAs that are managing the human genome. Explanatory article here.)
  • COVID-19 vaccines – An Australian Review
    https://www.opastpublishers.com/open-access-articles/covid19-vaccinesan-australian-review.pdf
    (This scathing paper has to be read to be believed but here’s the big takeaway: “mRNA vaccines are neither safe nor effective, but outright dangerous.” Summary article here.)
  • National Academies Committee on Review of Relevant Literature Regarding Adverse Events Associated with Vaccines March 30 2023: Written material accompanying oral remarks.
    https://www.researchgate.net/publication/369755622_National_Academies_Committee_on_Review_of_Relevant_Literature_Regarding_Adverse_Events_Associated_with_Vaccines_March_30_2023_Written_material_accompanying_oral_remarks
    (“These comments contain a number of novel analyses conducted relating to Covid-19 vaccine safety.”)
  • Is the US’s Vaccine Adverse Event Reporting System broken?
    https://www.bmj.com/content/383/bmj.p2582

…FROM:    https://ladycasey.substack.com/p/scientific-studies-on-vaccine-injuries?utm_source=substack&utm_campaign=post_embed&utm_medium=email

sa-mRNA — What is it?

What is self-amplifying mRNA?

And it is already being used in Japan and maybe soon in the US. It combines the unknown duration of effect of mRNA with the mutation-producing effects of nuclear DNA.

Here is what the Perplexity AI says. Note that it can be called self-amplifying DNA also:

Self-amplifying DNA refers to a type of DNA-based vaccine platform that combines elements of conventional DNA vaccines with the self-replicating capabilities of RNA viruses. Here are the key points about self-amplifying DNA:

  1. Structure and components:
    • It is a circular double-stranded DNA molecule
  • Contains a strong promoter (e.g., human cytomegalovirus immediate early promoter)

Encodes viral replicase genes, typically from alphaviruses or flaviviruses. Includes the gene of interest (GOI) encoding the vaccine antigen

  • Mechanism of action:
    • After delivery into cells, the DNA is transcribed in the nucleus to produce self-amplifying RNA
  • This RNA is transported to the cytoplasm where it self-replicates and produces high levels of the antigen
  • The self-amplification process mimics viral infection, leading to sustained antigen production
  • Advantages:
    • Combines benefits of DNA vaccines (stability, ease of production) with self-amplifying RNA technology

Requires lower doses compared to conventional DNA or mRNA vaccines

  • Induces potent humoral and cellular immune responses
  • More stable than RNA, simplifying storage and distribution
  • Delivery methods:
    • Can be delivered as naked DNA, often using electroporation for improved cellular uptake
  • Can also be formulated with lipid nanoparticles (LNPs) for enhanced delivery
  • Applications:
    • Promising platform for rapid vaccine development against emerging infectious diseases
  • Potential for use in therapeutic cancer vaccines and other applications
  • Self-amplifying DNA, also referred to as DNA-launched replicons (DREPs), represents an innovative approach in vaccine technology that aims to combine the advantages of DNA vaccines with the potency of self-amplifying RNA systems.

I was asked to expand on this idea. I don’t want to alarm unnecessarily nor fail to alarm when appropriate. Let me give an example: how I approached the COVID mRNA vaccines before they were released.

  1. I was worried about them but there were noreal data to go on
  2. I assisted Dr. Sin Hang Lee in his petition (as editor) to the FDA to try and stop them in Nov 2020 on the basis that the Pfizer trials were not conducted per existing standards
  3. I shared information from Dr. Patrick Whelan on my blog about problems that might be anticipated.
  4. I did NOT tell people not to take them. I warned them about problem that might be anticipated.
  5. Later I did warn people, once the problems became clearer, in January 2021 and later. I was one of the first to issue warnings, as soon as I could identify problems.

Looking back, I wish I had issued stronger warnings. But I had no reason to think the vaccines would be as bad as they were.

Right now I am looking at a theoretical vaccine construct. I’m worried. But I don’t know how worried to be. I have no human data. But Japanese doctors, where these vaccines are already being made and used, have warned that they are a disaster.

How big a disaster, I don’t know. I hope to find out in September when I will be in Japan, speaking at the ICS 6 Conference in Tokyo with the Japanese doctors who are speaking out, if not before.

And now we learn that CSL Sequirus is involved in the Japanese vaccine. BTW, 6 cases of chest pain in 828 subjects shortly after vaccination were blown off by the investigators. The control vaccine was Comirnaty, which would (naturally) make comparator vaccines look not too bad.

Here is the rest of this press release:

The approval is based on positive clinical data from several ARCT-154 studies, including an ongoing 16,000 subject efficacy study performed in Vietnam as well as a Phase 3 COVID-19 booster trial, which achieved higher immunogenicity results and a favorable safety profile compared to a standard mRNA COVID-19 vaccine comparator.  Initial study results have been published in MedRxiv and are expected to be published in a peer-reviewed journal by the end of the year.

[Here is the preprint: https://www.medrxiv.org/content/10.1101/2023.07.13.23292597v1]

“We are proud of the role that Arcturus has played in this collaboration to develop and validate the first approved sa-mRNA product in the world,” said Joseph Payne, Chief Executive Officer of Arcturus Therapeutics. “This approval for the sa-mRNA COVID-19 vaccine is a major achievement, and we are excited to embark on future endeavors that utilize our innovative sa-mRNA vaccine platform alongside our global exclusive partner, CSL.”

CSL’s vaccine business, CSL Seqirus, one of the largest influenza vaccine providers in the world, partnered exclusively with Meiji Seika Pharma for distribution of the sa-mRNA COVID vaccine, ARCT 154, in Japan.

“Our expertise in seasonal and pandemic influenza positions us well to help the global community reduce the burden of COVID-19 and we look forward to playing a key role in helping protect the people of Japan,” said Stephen Marlow, Senior Vice President and General Manager of CSL Seqirus.

About sa-mRNA
Messenger RNA (mRNA) vaccine technology protects against infectious diseases by instructing cells in the body to make a specific protein, stimulating the immune response, and leaving a blueprint to recognize and fight future infection. However, sa-mRNA makes copies of the mRNA which generates the production of more protein compared to an equivalent amount of mRNA in a vaccine.  The technology has the potential to create more potent cellular immune responses and increase duration of protection, while using considerably lower doses of mRNA.

About CSL
CSL (ASX:CSL; USOTC:CSLLY) is a global biotechnology company with a dynamic portfolio of lifesaving medicines, including those that treat haemophilia and immune deficiencies, vaccines to prevent influenza, and therapies in iron deficiency and nephrology. Since our start in 1916, we have been driven by our promise to save lives using the latest technologies. Today, CSL – including our three businesses: CSL Behring, CSL Seqirus and CSL Vifor – provides lifesaving products to patients in more than 100 countries and employs 32,000 people. Our unique combination of commercial strength, R&D focus and operational excellence enables us to identify, develop and deliver innovations so our patients can live life to the fullest. For inspiring stories about the promise of biotechnology, visit CSLBehring.com/Vita and follow us on Twitter.com/CSL. For more information about CSL, visit www.CSL.com.

About Arcturus Therapeutics
Founded in 2013 and based in San Diego, California, Arcturus Therapeutics Holdings Inc. (Nasdaq: ARCT) is a global late-stage clinical mRNA medicines and vaccines company with enabling technologies: (i) LUNAR® lipid-mediated delivery, (ii) STARR® mRNA Technology (sa-mRNA) and (iii) mRNA drug substance along with drug product manufacturing expertise. The Company has an ongoing global collaboration for innovative mRNA vaccines with CSL Seqirus, and a joint venture in Japan, ARCALIS, focused on the manufacture of mRNA vaccines and therapeutics. Arcturus’ pipeline includes RNA therapeutic candidates to potentially treat ornithine transcarbamylase deficiency and cystic fibrosis, along with its partnered mRNA vaccine programs for SARS-CoV-2 (COVID-19) and influenza. Arcturus’ versatile RNA therapeutics platforms can be applied toward multiple types of nucleic acid medicines including messenger RNA, small interfering RNA, circular RNA, antisense RNA, self-amplifying RNA, DNA, and gene editing therapeutics. Arcturus’ technologies are covered by its extensive patent portfolio (patents and patent applications issued in the U.S., Europe, Japan, China, and other countries). For more information, visit www.ArcturusRx.com. In addition, please connect with us on Twitter and LinkedIn.

from:    https://merylnass.substack.com/p/what-is-self-amplifying-mrna?publication_id=746368&post_id=147039126&isFreemail=true&r=19iztd&triedRedirect=true&utm_source=substack&utm_medium=email

Concerning Blood Pressure

The Great Blood Pressure Scam

Exploring the Forgotten Causes and Treatments of Hypertension and the Dangers of BP Medications

Story at a Glance:

•Elevated blood pressure is the most common chronic disease, and as the decades go by more and more people are declared hypertensive.

•Remarkably, at least 25% of all hypertension diagnoses are due to inaccurate measurements, and there is still no known reason for why over 90% of people are hypertensive.

•Aggressively treating everyone’s blood pressure is justified under the belief it prevents cardiovascular disease. However, in most cases it has never been proven to reduce heart disease—rather it only leads to a small reduction in strokes (hence why these medications were rebranded to treat “cardiovascular disease”).

•Many of the misunderstandings with heart disease arise from the fact that impaired circulation or damage to the blood vessels will cause blood pressure to go up and their correlation being misinterpreted to instead believe high blood pressure causes cardiovascular disease.

•In this article, we will discuss the actual causes of high blood pressure, the dangers of commonly used blood pressure medications, the safest pharmaceutical and natural ways to reduce blood pressure directly, and our preferred methods for treating the underlying causes of high blood pressure.

Ever since I first encountered the medical field, something struck me as off about their relentless focus on blood pressure. Before long, I began to notice that the blood pressures the same acquaintances (e.g., relatives or friends) shared with me varied immensely. As I was pondering this, a long-time Eastern spiritual teacher shared with me their belief that the West’s relentless focus on blood pressure was due to it being much easier to measure than blood perfusion (healthy blood flow).

Then, as I became more acquainted with the medical field, I began to notice a consistent pattern—whenever a drug existed that could treat a number or statistic, as the years went by, the acceptable number kept on being narrowed, making more and more people eligible to take the drugs that treated the number.

For example, as I discussed recently, once the statins drugs entered the market (which unlike their predecessors, could effectively lower cholesterol), the acceptable blood cholesterol levels kept on being lowered, and before long almost everyone was told they would die from a heart attack unless they started a statin—despite statins have an almost non-existing mortality benefit (e.g., taking them for 5 years at best makes you live 3-4 days longer) and causing (often severe) side effects for roughly 20% of users. Broadly recommending these drugs hence appears unconscionable, but as I showed in that article, these unjustifiable guidelines were a product of clever pharmaceutical marketing and targeted bribery of public officials.

In this article, I will attempt to show how something similar happened in the field of blood pressure. As this is an immensely controversial position to take (e.g., measuring and documenting blood pressure is one of the most routine procedures during a medical visit), I’ve done my best to clearly present the evidence for this perspective so you can make your own determination.

TO read the rest of the article, as well as so many other enlightening articles, go to:    https://www.midwesterndoctor.com/p/the-great-blood-pressure-scam?publication_id=748806&post_id=147019501&isFreemail=true&r=19iztd&triedRedirect=true&utm_source=substack&utm_medium=email

Hope for Dealing With the Vaccine Spike Protein

Study Proposes mRNA Vaccine Spike Protein Production Can Be Deactivated and Turned ‘Off’

The COVID shots are known to increase in lethality after repeated doses. The ‘vaccines’ are linked to turbocancers, reproductive destruction, miscarriages in pregnant women, paralyzation, tinnitus, increased excess death rates, autoimmune disorders in the thyroid, headaches, seizures, heart inflammation and more. Children who received mRNA ‘vaccines’ have also been affected. The mRNA jabs contain hundreds of times the allowable levels of DNA contamination leading to mutagenic effects that change genetic material and increase mutations, contaminating the blood supply, and permanently altering the DNA of the vaccinated and their offspring. Dr. Peter McCullough estimated that over 600,000 Americans have died from COVID ‘vaccines’. The jabs are expected to kill people for a very long time into the future.

The McCullough Foundation published a new study that proposes an intervention to turn off the mutagenic effects of COVID mRNA injections by using small interfering RNA (siRNA) to bind to COVID vaccine mRNA so that the body may eliminate it, and ribonuclease targeting chimeras (RIBOTAC) that can sandwich the mRNA. The introduction of siRNA and RIBOTAC may potentially prevent uncontrolled Spike protein production and reduce toxicity. The targeted nature of siRNA and RIBOTACs allows for precise intervention to inactivate and degrade residual vaccine mRNA, offering a path to prevent and mitigate adverse events of mRNA-based therapies. Dr. McCullough said that some siRNAs [pitirosan and incleanseran] are already used in practice and that he hopes that a biological technology company will produce RIBOTAC.

Dr. McCullough recommends his Base Spike Protein Detoxification protocol that includes nattokinase, bromelin, and curcumin that are available at the Wellness Company He said that nattokinase dissolves blood clots and gave dosages in the video.

mRNA from the jabs has been shown to circulate in the blood for at least 28 days and can be stuck in lymph nodes for at least two months. Spike proteins are said to be circulating at high levels, based on antibodies against the spike protein.

Moderna has had several more mRNA ‘vaccines’, including one for the flu, approved. More mRNA injections will make people more progressively sick because it is synthetic and resistant to the body breaking it down naturally.

 

 

.

A preprint study coauthored by Dr. Peter McCullough, published in May, described a novel method of deactivating the genetic alteration effects of the mRNA Covid vaccinations, providing hope to the billions of people who’ve been genetically mutated.

“The Pfizer-BioNTech and Moderna biodistribution studies refute the assertion that nanolipid-bound nms-mRNA remains in the deltoid muscle or axillary lymph nodes. Detectable vaccine mRNA levels remaining in various tissues raises potential safety concerns,” the study said in the ‘Conclusions’ section. “The possibility of vaccine mRNA integration into the host genome and the prospect of unintended protein production due to read through advocate for a mechanism to eliminate lingering synthetic mRNA and halt damaging Spike protein production. The use of siRNA and RIBOTACs to target and degrade vaccine mRNA are promising approaches to mitigate deleterious health effects. The ability to readily tailor the siRNA and RIBOTACs to target an mRNA of interest makes these techniques particularly appealing, although further investigation is warranted to address challenges which include possible off-target effects and immune system activation.”

Messenger RNA (mRNA) technology, referred to in Moderna’s patents as modified mRNA or mmRNA for modified messenger RNA, is an exotic technology that encapsulates an altered RNA sequence within a lipid nanoparticle so as to introduce it into the cells of the vaccinated individual. The foreign man-made sequence is then incorporated into the cells of the vaccinated individual, thus acting more as a gene therapy than a traditional vaccine.

While the exotic injection makes the individual begin to produce the dangerous Covid spike protein, currently there is no way to stop the individual from producing that spike protein forever. There is no ‘off’ switch, at least until now.

The study described a method of turning off the production of the spike protein.

“…the longevity of the encapsulated mRNA along with unlimited production of the damaging and potentially lethal Spike (S) protein call for strategies to mitigate potential adverse effects,” the study said in the ‘Abstract’ section. “Here, we explore the potential of small interfering RNA (siRNA) and ribonuclease targeting chimeras (RIBOTACs) as promising solutions to target, inactivate, and degrade residual and persistent vaccine mRNA, thereby potentially preventing uncontrolled Spike protein production and reducing toxicity. The targeted nature of siRNA and RIBOTACs allows for precise intervention, offering a path to prevent and mitigate adverse events of mRNA-based therapies.”

Read full article here…

Link for Study by Nicolas Hulscher, Dr. McCullough, and Diane E. Marotta:    https://osf.io/preprints/osf/qxbgu

from:    https://needtoknow.news/2024/06/study-proposes-mrna-vaccine-spike-protein-production-can-be-deactivated-and-turned-off/

REthinking Ivermectin

Ivermectin Found to Protect Against Many Various Diseases, Cancer, Vax Damage & EMF

Sean Miller | Infowars

Outside of being a horse dewormer, Ivermectin has been scientifically found to treat a list of various ailments in humans.

Ivermectin, a drug derived from a soil microbe, is perhaps best known for it’s treatment of Covid which made it a controversial prescription during the era when health officials were trying to get the Covid death numbers up.

One such case of ivermectin aiding a Covid patient was with 80-year-old Judith Smemthiewicz who got better after taking the drug in early 2021.

“…[she] was placed on a ventilator in late December,” an article by ABC’s WKBW said. “Initially doctors gave her one dose of the controversial drug Ivermectin, and she improved.”

study published in 2022 has found that Ivermectin inhibits tumor metastasis.

“Tumor metastasis is the major cause of cancer mortality; therefore, it is imperative to discover effective therapeutic drugs for anti-metastasis therapy. In the current study, we investigated whether ivermectin (IVM), an FDA-approved antiparasitic drug, could prevent cancer metastasis. Colorectal and breast cancer cell lines and a cancer cell-derived xenograft tumor metastasis model were used to investigate the anti-metastasis effect of IVM,” the study said in the ‘Abstract’ section. “Our results showed that IVM significantly inhibited the motility of cancer cells in vitro and tumor metastasis in vivo. Mechanistically, IVM suppressed the expressions of the migration-related proteins via inhibiting the activation of Wnt/β-catenin/integrin β1/FAK and the downstream signaling cascades. Our findings indicated that IVM was capable of suppressing tumor metastasis, which provided the rationale on exploring the potential clinical application of IVM in the prevention and treatment of cancer metastasis.”

Another study chronicled how Ivermectin can help prevent neurological disorders such as multiple sclerosis.

“The results evidenced that IVM and nano-IVM administration is capable of reducing demyelination in mice,” the study said in the ‘Conclusion’ section.

Demyelination is the loss of myelin in nervous system tissue. The study aimed to analyze ivermectin’s effects on the phenomenon.

“Multiple sclerosis (MS) is a chronic disease of the central nervous system (CNS) and its cause is unknown. Several environmental and genetic factors may have roles in the pathogenesis of MS,” the study said in the ‘Objectives’ section. “The synthesis of solid lipid nanoparticles (SLNs) for ivermectin (IVM) loading was performed to increase its efficiency and bioavailability and evaluate its ability in improving the behavioral and histopathological changes induced by cuprizone (CPZ) in the male C57BL/6 mice.”

One study chronicled the history of the drug, its technical characteristics, as well as a long list of ailments it has been documented to treat.

Myiasis, trichinosis, malaria, leishmaniasis, leishmaniasis, American trypanosomiasis, schistosomiasis, bedbugs, rosacea, asthma, epilepsy, neurological diseases, HIV, tuberculosis, buruli ulcer and anti-cancer properties have all been document with Ivermectin treatment, according to the study.

“There is a continuously accumulating body of evidence that ivermectin may have substantial value in the treatment of a variety of cancers. The avermectins are known to possess pronounced antitumor activity,107 as well as the ability to potentiate the antitumor action of vincristine on Ehrlich carcinoma, melanoma B16 and P388 lymphoid leukemia, including the vincristine-resistant strain P388,” the study said. “Over the past few years, there have been steadily increasing reports that ivermectin may have varying uses as an anti-cancer agent, as it has been shown to exhibit both anti-cancer and anti-cancer stem cell properties. An in silico chemical genomics approach designed to predict whether any existing drugs might be useful in tackling glioblastoma, lung and breast cancer, indicated that ivermectin may be a useful compound in this respect.”

Electromagnetic frequencies disrupt physiology and psychology, particularly in the Covid-vaccinated, but ivermectin has been found to remedy some of that disruption.

“Recognizing that humans in the modern age are regularly bombarded with electromagnetic frequencies (EMFs) and other toxins that disrupt proper nervous system function, ivermectin might be worth taking for preventative purposes to keep the nervous system optimized through stabilization of P2X4 receptors,” Ethan Huff wrote for Natural News. “Stabilizing P2X4 receptors is important because expression of P2X4 is a major driving factor in ALS, Parkinson’s, Alzheimer’s, chronic neuropathic pain, migraines, epilepsy, depression, bipolar disorder, schizophrenia and anxiety.”

from:    https://www.infowars.com/posts/ivermectin-found-to-protect-against-many-various-diseases-cancer-vax-damage-emf/

What Happened to Real Cow’s Milk???

Frankenfoods v2: Exploiting the Bioequivalence Principle

Frankenfoods v2: Exploiting the Bioequivalence Principle
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Powerful forces are trying to shift our food system away from the soil-based farming systems and towards genetically engineered, lab-grown food. We can’t let them succeed.


THE TOPLINE

  • Bored Cow, a cow and animal free whey-containing, cultured milk, is one of a growing number of foods being produced through synthetic biology and ‘precision fermentation’—the health risks of which are largely unknown.
  • We’re told products like Bored Cow are fine—even desirable—because they’re biologically the same as their natural counterparts without the toll on the environment purportedly caused by livestock and dairy farming.
  • Yet the evidence indicates that these products are far from biologically equivalent, but regulators don’t seem to care.

Got Milk GE-yeast-fermented-whey-protein drink?

You may have heard about the new “animal-free dairy milk” called Bored Cow. It’s being billed as a more animal and environmentally friendly option to traditional milk that comes from a ruminant’s udders. It all sounds great until you dig a bit deeper to learn that it is produced using synthetic biology (synbio), using genetically engineered (GE) yeast that is then put into a so-called ‘precision fermentation’ system. While the whey protein in it is the same as that found in cow’s milk, that’s only a small part of the overall story. Emerging data from some scientists, like John Fagan from the Health Research Institute (HRI), says the fermentation isn’t as precise as claimed, and there’s a lot of other compounds in the milk, some of which have never been recorded by science before. That might mean that drinking Bored Cow ‘milk’ on a daily basis could have unknown and potentially dangerous human health implications. This might just be one product, but it matters because powerful special interests are working to make synbio the tech platform of our food system moving forward—where farms are replaced with fermentation tanks—in the name of protecting the environment.

What’s happening here is an effort to get consumers to believe they can enjoy all the flavor, mouth feel, and nutrition of real cow’s milk…without the involvement of any cows (hence the “Bored Cow” name). Bored Cow is made with whey protein produced through a process called “precision fermentation,” a form of synbio. This involves taking a gene for whey protein and inserting it into a GE yeast. The yeast is put into fermentation tanks with other nutrients to help it grow. At the end the GE yeast is supposed to be filtered out, leaving only the milk protein. Bored Cow takes this protein and adds vitamins, minerals, and other ingredients to mimic the taste, consistency, and nutritional content of real cow’s milk.

Far from ‘bioequivalent’

The marketing hype behind Bored Cow starts falling apart when you learn that it’s not even close to being equivalent to real milk from pasture. HRI’s independent testing found 92 unknown compounds in this synbio milk. Fagan, HRI’s chief scientist, said these compounds are “completely novel to our food…They are nutritional dark matter.”

The FDA must be on top of this, right? Wrong. Bored Cow has not undergone safety testing at the FDA. Perfect Day, the manufacturer of the synbio whey protein, determined it was “generally recognized as safe” (GRAS) and voluntarily notified the FDA of this determination; in response the FDA said it had no questions. Given how rife the GRAS process is with conflicts of interest, this is akin to taking the company’s word for it that its novel synbio whey protein is safe.

Nor is it very likely that Bored Cow is nutritionally equivalent to real milk. Just as meat is more than just protein, milk is far more than a simple combination of whey and various vitamins and minerals. Milkfat contains 400 different fatty acids. Milk has two types of proteins, whey and casein—and there are several different types of these two proteins contained in milk, and a whole bundle of other compounds like lactoferrin and bioactive peptides that help prime the immune system.

Does synbio milk have this nutritional complexity? It doesn’t seem like it, as casein, to use just one example, which comprises 80 percent of the protein in cow’s milk, isn’t listed as an ingredient. Further, according to HRI’s tests, the amino acid composition of Bored Cow is “strikingly different” than that of milk.

Laws not fit to purpose

Bored Cow is representative of a whole new generation of GE foods that are in development, some of which we’ve written about previously. Older genetically modified (GM) foods were created by modifying the genome of a living plant by inserting, for example, an herbicide-resistance trait. That was nothing compared to what’s going on now. GE yeast or fungi are being used as little factories to manufacture food components that regulators say are biologically equivalent to their natural counterparts, so, they say, no additional testing is required because the foods have been shown to be safe through their long history of consumption. But, as we’ve seen, getting a yeast to make one protein found in milk, fermenting it, then adding nutrients, and slapping “milk” on the label doesn’t make it milk. Nor, for that matter, is lab-grown meat biologically equivalent to pasture-raised meat.

And herein lies the problem. The entire framework for dealing with genetically engineered foods in the US is fundamentally broken. That’s because the federal government decided decades ago that the final product is all that matters, not the process used to create that product. This was codified in the 1986 Coordinated Framework for the Regulation of Biotechnology, which was updated in 1992 and again in 2017. Astoundingly, it wasn’t updated to install more robust safety measures to protect Americans from new and previously unthinkable forms of food. It was updated in large part to remove or mitigate “unnecessary costs and burdens” that “limit the ability of technology developers” to “navigate the regulatory process” which also “hamper economic growth, innovation, and competitiveness.” That is, the Framework was updated to make it easier for the biotech industry to ger their frankenfoods onto our dinner plates!

We’re worried that what’s coming are further “updates” to this framework that allow GE foods and those developed using synbio technologies to be considered “bioequivalent” to their natural counterparts—in essence, drinking the lab-grown food industry’s Kool-Aid. If regulators determine that synbio milk is equivalent to real milk, will consumers be allowed to make their own choices, or will we be sold out as we were with the sham GMO labeling law that allowed companies to hide the GM contents of their food in scannable codes?

Some countries are already moving in that direction: Costa Rica just adopted new regulations which treat a wide-range of gene edited products as equivalent to conventionally-bred products. This is something we have to keep a keen eye on.

The advent of lab-grown meat, plant-based meat, and products like Bored Cow show how inadequate our current laws are in dealing with these foods. Of course it matters how these foods are made! CRISPR, the gene-editing technology, is known to produce unintended outcomes. What evidence is there that eating food grown in laboratories from genetically modified yeast—food that is significantly different than the food we have evolved to eat over human history—is safe, much less healthy?

Put simply, the fake meat and milk synbio manufacturers are exploiting old rules never intended for synbio products so they can escape doing any safety testing before their products hit the market. They’re using all-too-familiar revolving doors with the FDA to get their way, and they want to deceive us into thinking they’re saving the planet from those nasty, carbon dioxide-producing animals while offering us foods that are as safe and healthy as those produced on real farms with the help of real animals—without any of it.

We’re watching these developments closely, and we’ll alert you as soon as we see an opportunity to take political action on this critical issue. In the meantime, please share this article widely, as we need a lot more awareness of how synbio makers are using the principle of ‘bioequivalence’ to get their questionable foods into our mouths.

from:    https://anh-usa.org/frankenfoods-v2-exploiting-the-bioequivalence-principle/

The Pfizer-Spider Web is Growing

Pfizer’s New Heart Pandemic

Is Accountability Coming?

___________________________________________________________________
Originally posted on The Tenpenny Report by Fed Up Texas Chick; Updated by Dr. Sherri Tenpenny

For years, we’ve been writing about how evil Pfizer is. Case in point: this article from 2017 where we featured Dr. Peter Rost, a former vice president of Pfizer and a pharmaceutical industry whistleblower. He is the author of The Whistleblower, Confessions of a Healthcare Hitman, and at the time was talking about how deadly the HPV vaccine was. Dr. Rost claimed that pharmaceutical companies intentionally design vaccines to keep the public in a state of illness for purposes of perpetual treatments.

That was seven years ago, and never has the evil of Pfizer been more apparent. In January 2024, the powers-that-be declared that the new coronavirus variant would likely cause a higher risk of heart problems.

This time, they presented research from RIKEN, Japan’s largest scientific institute, funded nearly entirely by the Japanese government. However, Riken also accepts “donations from individuals and corporations for the enhancement and development of research.” They even have a page where donors can send a direct credit card donation.

I’m sure that is all above board. In 2019, RIKEN had a budget of $900 million, yet they still needed credit card donations?

What types of corporations work with RIKEN? Corporations like Bayer work with RIKEN, like in the drug discovery collaboration they’ve been jointly working on for about five years.

In December 2021, Pfizer announced they would buy Arena Pharmaceuticals. Pfizer had its eye on etrasimod, Arena’s drug for ulcerative colitis. The drug was approved by the FDA in October 2023, and Pfizer now markets it as VELSIPITY™. Pfizer’s website says in the press release that “UC is a chronic and often debilitating condition that affects an estimated 1.25 million people in the United States.”

That’s a lot of people, but is it enough of a market to drive Pfizer to buy Arena at a 100% premium, a $6.7 billion cash deal? That doesn’t add up in my book. Pfizer sped the development of etrasimod because the drug is a potential therapy for all kinds of immuno-inflammatory diseases, including inflammation of the heart. Part of the deal was that Pfizer acquired all Arena assets in gastroenterology, dermatology, and cardiology.

The first links between the COVID-19 mRNA jabs and myocarditis began to be reported in July 2021. In December 2021, Pfizer entered into a formal agreement to purchase Arena, and by March 2022, it was a done deal.

Incredibly, myocarditis incidents began skyrocketing shortly thereafter. In one example from a May 2022 article, emergency cardiac arrest calls for young adults strongly correlated with the vaccine rollout of doses 1 and 2 in Israel, one of the most jabbed countries in the world.

An FDA-sponsored study looked at health records of children from December 2020 to June 2022 and found incidences of myocarditis and pericarditis to be high enough to trigger a safety signal in 12- to 17-year-olds. The timeframe from the jab to seeking cardiac care for myocarditis or pericarditis was 6.8 days. In a literature review from 2020 to 2022, males were approximately seven times more likely than females to present myocarditis/pericarditis. Another recent study concluded that a booster dose is associated with increased myocarditis risk in adolescents and young adults.

Cancer

In early 2023, Pfizer announced another huge deal with purchase of Seagen Pharmaceuticals.

Seagen is known for its pipeline of cancer drugs, and Pfizer really wanted that pipeline because they spent $43 billion on the deal. Pfizer Chairman and CEO Albert Bourla described it as “acquiring the goose that is laying the golden eggs.”

Once again, the purchase begs the question: Is this business prowess on the part of Pfizer, or is it all planned?

The concept of “turbo cancer” was introduced in January 2023 when fact-checkers across the internet began reporting that any connection between the mRNA jabs and turbo cancer was false. By summer, physicians started describing turbo cancers as the new pandemic, and scientists started to provide reasoning for the sudden and aggressive cancers that oncologists were witnessing.

They seemed to start after a COVID-19 booster shot in all cases. Soon, articles like this one were commonplace, with physicians professing they had never seen cancers with this form of aggression who were often dead within a few months, weeks, or sometimes, even days.

Bourla himself said that the world is experiencing a new type of cancer epidemic, which may explain the Seagen purchase. Seagen works with antibody-drug conjugate (ADC) technology, which uses monoclonal antibodies made to seek out cancer cells and deliver a drug to those cells while sparing the surrounding tissue. Bourla called the ADC technology “one of the greatest technologies to battle cancer” and said they were “very much like the mRNA for vaccines.”

Interestingly, Pfizer created the first ADC, Mylotarg, but had to remove it from the market in 2010 after studies showed the drug was more toxic than chemotherapy.

Bourla said the Seagen acquisition will “dramatically change the oncology presence of Pfizer, making it one of a kind. Seagen’s cancer therapy will bring cancer treatment to the world at a scale that has not been seen before.”

Problem. Reaction. Solution.

Unadulterated Greed

Pfizer was literally flooded with cash after 2021.

Pfizer’s revenues in 2021 were double their revenues from 2020 ($81.3 billion). In 2022, they bought Biohaven Pharmaceuticals for $11.6 billion to gain access to the company’s migraine drug. That same year, they also purchased Global Blood Therapeutics to gain access to the company’s sickle cell drug Oxbryta. But only approximately 100,000 Americans suffer from sickle cell; how can they make $3 billion off this drug? What does Pfizer know that the rest of us don’t? Will we see a blood cell disease epidemic as well?

Some analysts note that, ultimately, Pfizer may go bankrupt with all the lawsuits on the horizon. Will Pfizer go the way of Purdue Pharma, a company where greed and dishonesty allowed it to continue marketing harmful products to the public? Just as with Purdue, will Pfizer lose its legal protections when the millions of vaccine injury claims and charges of fraud land on Bourla’s desk?

The days of huge revenues from COVID-19 products have passed. The US government is returning $3.5 billion of unused Paxlovid treatments, and Pfizer is facing revenue losses from many patent expirations and unfulfilled government contracts worldwide.

Vigilant News noted that older, more experienced vaccine companies such as GSK did not enter the COVID-19 vaccine fray. That looks like it was a wise choice. However, they no doubt got paid well for sitting this one out.

Today, Pfizer’s stock is far less valuable than it was just a few years ago, despite the flashy acquisitions of companies like Arena and Seagen and the billions of dollars made from the COVID death jabs. In the last year, Pfizer has underperformed by 35% compared to the overall pharmaceuticals index.

We can only hope Pfizer – and all other players such as doctors, nurses, pharmacists, politicians, and governments will have soon pay dearly for their folly. That is the heart of the matter.

from:    https://drtenpenny.substack.com/p/pfizers-new-heart-pandemic?publication_id=931759&post_id=145808579&isFreemail=true&r=19iztd&triedRedirect=true&utm_source=substack&utm_medium=email

Cholesterol, Statins, & Heart Disease

This is a highly abbreviated version of the total article.  Go to the Link (https://www.midwesterndoctor.com/p/the-great-cholesterol-scam-and-the?publication_id=748806&post_id=146062962&isFreemail=true&r=19iztd&triedRedirect=true&utm_source=substack&utm_medium=email) to read the rest:

 

The Great Cholesterol Scam and The Dangers of Statins

Exploring the Actual Causes and Treatments of Heart Disease

Story at a Glance:

•There is a widespread belief that elevated cholesterol is the “cause” of cardiovascular disease. However, a large body of evidence shows that there is no association between the two and that lower cholesterol significantly increases one’s risk of death.

•An alternative model (which the medical industry buried) proposes that the blood clots the body uses to heal arterial damage, once healed, create the characteristic atherosclerotic lesions associated with heart disease. The evidence for this model, in turn, is much stronger than the cholesterol hypothesis and provides many important insights for treating heart disease.

•The primary approach to treating heart disease is to prescribe cholesterol lowering statin drugs (to the point, over a trillion dollars have now been spent on them). Unfortunately, the benefits of these highly toxic drugs are minuscule (e.g., at best taking them for years extends your life by a few days) and the harms are vast (statins are one of the most common pharmaceuticals that severely injure patients).

•In this article we will explore the specific injuries caused by statin drugs, the forgotten causes of cardiovascular disease, and our preferred treatments for heart and vascular diseases.

The more I study science, the more I come to see how often fundamental facts end up being changed so that a profitable industry can be created. In the case of heart disease, I very much believe that is the case and in this publication, I’ve tried to expose the erroneous information that predominates our understanding of this subject (e.g., previously I’ve discussed why our model of how the heart pumps blood in the body is incorrect and in an article that will be released in a few weeks, I will detail the major misconceptions about blood pressure management).

Within cardiology, I believe one of the most damaging falsehoods is that cholesterol causes heart disease and that taking statins (or their newer equivalents), which lower cholesterol, are the key to preventing heart disease. This is because, in addition to those “facts” being incorrect, statins are also some of the most dangerous and widely used pharmaceutical drugs on the market.

The Forgotten Side of Medicine is a reader-supported publication. To receive new posts and support my work, consider becoming a free or paid subscriber. To see how others have benefitted from this newsletter, click here.

Cholesterol and Heart Disease

Frequently, when an industry harms many people, it will create a scapegoat to get out of trouble. Once this happens, a variety of other sectors that also benefit from that scapegoat existing will jump on the bandwagon. Before long, a false belief that harms society becomes an unquestionable dogma that becomes very difficult to overturn because many corrupt parties have a vested interest in maintaining the lie.

For example, various easily addressable factors (which often exist in the first place because they benefit an industry) are responsible for the chronic diseases we face in society and our vulnerability to infectious diseases (e.g., the obese and diabetics were much more likely to catch COVID-19). However, by saying all diseases result from insufficient vaccination, it gets all those destructive industries off the hook and creates a huge market for selling vaccines and treatments for these illnesses. Thus, since there are so many vested interests behind the vaccine paradigm, it is very difficult to overturn—despite the fact the existing evidence shows vaccinations are responsible for the massive epidemic of chronic disease that is sweeping our country.

In the 1960s and 1970s, a debate emerged over what caused heart disease. On one side, John Yudkin effectively argued that the sugar being added to our food by the processed food industry was the chief culprit. On the other side, Ancel Keys (who attacked Yudkin’s work) argued that it was due to saturated fat and cholesterol.

Note: a case can also be made that the mass adoption of vegetable oils lead to this increase in heart disease. Likewise, some believe the advent of water chlorination was responsible for this increase.

Ancel Keys won, Yudkin’s work was largely dismissed, and Keys became nutritional dogma. A large part of Key’s victory was based on his study of seven countries (Italy, Greece, Former Yugoslavia, Netherlands, Finland, America, and Japan), which showed that as saturated fat consumption increased, heart disease increased in a linear fashion.

However, what many don’t know (as this study is still frequently cited) is that this result was simply a product of the countries Keys chose (e.g., one author illustrated that if Finland, Israel, Netherlands, Germany, Switzerland, France, and Sweden had been chosen, the opposite would have been found).

Fortunately, it gradually became recognized that Ancel Keys did not accurately report the data he used to substantiate his arguments. For example, recently an unpublished 56 month randomized study of 9,423 adults living in state mental hospitals or a nursing home (which made it possible to rigidly control their diets) that Keys was the lead investigator of was unearthed. This study (inconveniently) found that replacing half of the animal (saturated) fats they ate with vegetable oil (e.g., corn oil) lowered their cholesterol, and that for every 30 points it dropped, their risk of death increased by 22 percent (which roughly translates to each 1% drop in cholesterol raising the risk of death by 1%)—so as you can imagine, it was never published.

Note: the author who unearthed that study also discovered another (unpublished) study from the 1970s of 458 Australians, which found that replacing some of their saturated fat with vegetable oils increased their risk of dying by 17.6%

Likewise, recently, one of the most prestigious medical journals in the world published internal sugar industry documents. They showed the sugar industry had used bribes to make scientists place the blame for heart disease on fat so Yudkin’s work would not threaten the sugar industry. In turn, it is now generally accepted that Yudkin was right, but nonetheless, our medical guidelines are still largely based on Key’s work.

However, despite a significant amount of data that now shows lowering cholesterol is not associated with a reduction in heart disease (e.g., this studythis studythis studythis reviewthis review, and this review) the need to lower cholesterol is still a dogma within cardiology. For example, how many of you have heard of this 1986 study which was published in the Lancet which concluded:

During 10 years of follow-up from Dec 1, 1986, to Oct 1, 1996, a total of 642 participants died. Each 1 mmol/L increase in total cholesterol corresponded to a 15% decrease in mortality (risk ratio 0–85 [95% Cl 0·79–0·91]).

Note: when people are diabetic (which leads to the liver having to process too much sugar) the liver will convert to fat and then create more cholesterol to transport some of that fat. In these instances, I would argue the actual issue is an excess of sugar rather than elevated cholesterol levels it causes.

Statins Marketing

One of the consistent patterns I’ve observed within medicine is that once a drug is identified that can “beneficially” change a number, medical practice guidelines will gradually shift to prioritizing treating that number and before long, rationals will be created that require more and more of the population to be subject to that regimen. In the case of statins, prior to their discovery, it was difficult to reliably lower cholesterol, but once they hit the market, research rapidly emerged stating that cholesterol was more and more dangerous and, hence that more and more people needed to be on statins.  …

Here is the link for the continuation of the article :    https://www.midwesterndoctor.com/p/the-great-cholesterol-scam-and-the?publication_id=748806&post_id=146062962&isFreemail=true&r=19iztd&triedRedirect=true&utm_source=substack&utm_medium=email

Dealing with Post Jab Issues

Breakthrough Study Uncovers ‘Off Switch’ for COVID mRNA Shots

Analysis by Dr. Joseph Mercola
off switch covid mrna shots

STORY AT-A-GLANCE

  • A preprint study led by Dr. Peter McCullough suggests using siRNA and RIBOTACs to target and degrade residual mRNA from COVID-19 vaccines, potentially mitigating long-term health risks associated with persistent spike protein production
  • COVID-19 mRNA vaccines have shown wider distribution in the body than initially claimed, raising concerns about unintended effects and the need for an “off switch” to stop ongoing spike protein production
  • The study proposes using siRNA and RIBOTACs as potential methods to bind to and degrade vaccine mRNA in cells, offering a targeted approach to prevent adverse events from mRNA-based therapies
  • “Long vax” symptoms, similar to long COVID, have been reported following vaccination, including fatigue, brain fog, numbness, and cardiovascular issues, highlighting the need for effective treatments for those affected
  • Another study led by McCullough found a significant increase in cerebral thromboembolism risk associated with COVID-19 vaccines compared to other vaccines, leading to calls for a moratorium on their use

A preprint study revealed a potential way to clear out mRNA from COVID-19 shots. The research, led by cardiologist, internist and epidemiologist Dr. Peter McCullough, offers hope for those who are suffering from health damage caused by COVID-19 injections.

“As the world is waking up to nearly two thirds with potential future disease and disability from the long-lasting mRNA coding for the dangerous Wuhan spike protein, the search is on for ways to stop this molecular monster from doing more damage,” McCullough writes.1

The technique involves the use of small interfering RNA (siRNA) and ribonuclease targeting chimeras (RIBOTACs) to “target, inactivate, and degrade residual and persistent vaccine mRNA” and in so doing, help prevent uncontrolled spike protein production while reducing toxicity.2

Technique May Help Mitigate Damage Triggered by mRNA COVID Shots

Pfizer-BioNTech and Moderna studies show that mRNA from COVID-19 shots, which is carried by tiny particles called nanolipids, does not stay only in the shoulder muscle or nearby lymph nodes as initially claimed. Instead, the mRNA can be found in various tissues in the body, raising safety concerns.

There is a worry that this mRNA might integrate into the body’s DNA or cause unintended spike protein production, which could be harmful. To address these concerns, scientists are looking at ways to eliminate this leftover mRNA to stop the production of the spike protein, which the COVID-19 shot mRNA helps produce.

“Without any way to turn off the messenger RNA, we think every single messenger RNA shot, because it’s been made synthetic and resistant to human breakdown, is going to make people progressively sick,” McCullough says. “We have to find a way to get this out of the body … We’re gonna need an off switch for this.”3

McCullough’s study highlights “emerging concerns regarding the wide systemic biodistribution of these mRNA vaccines leading to prolonged inflammatory responses and other safety concerns.”4 According to the scientists, “The stability of mRNA vaccines, their pervasive distribution, and the longevity of the encapsulated mRNA along with unlimited production of the damaging and potentially lethal Spike (S) protein call for strategies to mitigate potential adverse effects.”5

The study reviews a strategy involving siRNA and RIBOTACs. “It may seem unfathomable for doctors to inject more RNA to deactivate Pfizer and Moderna synthetic mRNA that has accumulated in the body after multiple injections,” McCullough says. “However, siRNA used today in my practice (patisiran, inclisiran) appears to be safe and well-tolerated only notable for injection site reactions.”6

siRNA and RIBOTACs May Act as Off Switch for COVID mRNA Shots

siRNA is a type of RNA molecule that can specifically bind to and degrade messenger RNA (mRNA) in cells. This process prevents the mRNA from being used to produce proteins. siRNA works by entering the cell and becoming part of a complex called the RNA-induced silencing complex (RISC).

Within RISC, the siRNA pairs with its matching mRNA sequence and guides the complex to cut and destroy the target mRNA, stopping protein production. siRNA is used in research and therapeutic applications to silence specific genes, helping to study gene function and treat diseases caused by overactive or harmful genes.

RIBOTACs, meanwhile, are synthetic molecules designed to bind to specific RNA molecules and recruit natural cellular enzymes, called ribonucleases, to degrade the target RNA. RIBOTACs enter the cell and attach to both the target RNA and the ribonuclease enzyme. This binding brings the enzyme into close proximity with the target RNA, allowing the enzyme to cut and degrade the RNA.

RIBOTACs are used to specifically target and destroy RNA molecules that are involved in disease processes, providing a precise way to reduce the levels of harmful proteins produced by these RNAs. According to the study, “The targeted nature of siRNA and RIBOTACs allows for precise intervention, offering a path to prevent and mitigate adverse events of mRNA-based therapies.”7

The study described two methods to target and degrade residual and persistent COVID-19 shot mRNA, including siRNA Therapy (A) and RIBOTAC neutralization (B):8

“A: siRNA targeted against COVID-19 vaccine mRNA enters the vaccinated cell via LNPs [lipid nanoparticles], where it incorporates into the RISC. The siRNA in RISC binds to the complementary sequence of the target vaccine mRNA and cleaves it, thus suppressing spike protein production.

B: RIBOTACs targeted against COVID-19 vaccine mRNA enter the vaccinated cell via LNPs, where they bind to both the target vaccine mRNA and endogenous RNase. This results in RNase-mediated vaccine mRNA degradation and the suppression of spike protein production.”

“We use these small interfering RNAs already in practice,” McCullough said. “There’s one called Patisiran, the other one, Inclisiran. I use them in my practice. They only last in the body a few days. They bind up messenger RNA to inactivate it … We hope that some molecular technology companies can pick this up and consider this.”9

COVID-19 Shots Trigger Debilitating Adverse Events and ‘Long Vax’

An effective “off switch” could provide a lifeline for those suffering debilitating effects. Significant serious adverse events have occurred among many who received mRNA COVID-19 injections, which have also been said to have an “unacceptably high harm-to-reward ratio.”10

For every 1 million shots, an estimated 1,010 to 1,510 serious adverse reactions, such as death, life-threatening conditions, hospitalization or significant disability, may occur.11 When compared to the flu shot, data from the European Medicines Agency Eurovigilance Database shows that COVID-19 shots cause more:12,13

Allergic reactions Arrhythmia
General cardiovascular events Coagulation
Hemorrhages Gastrointestinal, ocular and sexual organ reactions
Thrombosis

Meanwhile, “long vax,” which describes an array of symptoms caused by COVID-19 shots, is finally getting some much-deserved recognition.

As reported by Science magazine in 2022, “In rare cases, coronavirus vaccines may cause long COVID-like symptoms,”14 which can include (but is not limited to) brain fog, memory problems, headaches, blurred vision, loss of smell, nerve pain, heart rate fluctuations, dramatic blood pressure swings and muscle weakness. The feeling of “internal electric shocks” are also reported.

Also in 2022, a preprint study from the U.S. National Institutes of Health reported new neuropathic symptoms that began in 23 adults within one month of receiving a COVID-19 shot.15 All of the patients felt severe tingling or numbness in their faces or limbs, and 61% also experienced dizziness when standing up, intolerance to heat and heart palpitations.

A study by Yale scientists also shed light on long vax, which they described as chronic post-vaccination syndrome, or PVS.16 In a study of 241 people who reported PVS after an mRNA COVID-19 shot, the median time from the jab to the onset of symptoms was three days, with symptoms continuing for 595 days. The five most common symptoms included:17

  • Exercise intolerance (71%)
  • Excessive fatigue (69%)
  • Numbness (63%)
  • Brain fog (63%)
  • Neuropathy (63%)

In the week before the survey was completed, patients reported a range of additional symptoms highlighting the mental toll the condition takes. The symptoms required a median of 20 interventions for treatment and included:18

Feeling unease (93%) Fearfulness (82%)
Overwhelmed by worries (81%) Feelings of helplessness (80%)
Anxiety (76%) Depression (76%)
Hopelessness (72%) Worthlessness (49%)

COVID mRNA Shots Linked to 111,795% Increase in Brain Clots

Adding to the urgency in uncovering a strategy to help those who have received COVID shots, another study led by McCullough revealed they’re linked to a 111,795% increase in brain clots known as cerebral thromboembolism.19

Cerebral thromboembolism, a known side effect of COVID-19 shots, is a medical condition where a blood clot (thrombus) forms in a blood vessel, travels through the bloodstream and becomes lodged in an artery supplying blood to the brain. This blockage prevents blood flow to parts of the brain, potentially leading to a stroke.

For the study, researchers used data from the U.S. Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration’s (FDA) Vaccine Adverse Event Reporting System (VAERS) covering January 1, 1990 to December 31, 2023. They compared cerebral thromboembolism cases reported after COVID-19 shots to those reported after flu shots and other vaccines.

The study found the risk of cerebral thromboembolism after COVID-19 vaccines is significantly higher compared to flu vaccines and all other vaccines.20 While there were 52 reports of cerebral thromboembolism associated with influenza vaccines, there were 5,137 cases linked to COVID-19 shots.21

The staggering increase led the researchers to call for “an immediate global moratorium on the use of COVID-19 vaccines,” particularly in women of reproductive age. McCullough wrote:22

“This paper did not capture the level of permanent neurologic devastation and disability suffered by these patients. I can tell you that the rates must be very high given the extensive nature of the blood clots reported. These data among others strongly support removing all COVID-19 vaccines and boosters from the market. No one should be put at risk for a serious stroke with any vaccine.”

Help for Those Injured by an mRNA COVID

It’s important to be wary of any new mRNA shots that come on the market and carefully weigh if the risks outweigh the reported benefits before getting one. However, if you’ve already had one or more COVID-19 shots, there are steps you can take to repair from the assault on your system.

The more mRNA shots you take, the greater the immune system damage. So, the first step is to avoid getting anymore mRNA jabs. Next, if you’ve developed any unusual symptoms, seek out help from an expert. The Front Line COVID-19 Critical Care Alliance (FLCCC) has a treatment protocol for post-jab injuries. It’s called I-RECOVER and can be downloaded from covid19criticalcare.com.23

Dr. Pierre Kory, who cofounded the FLCCC, has transitioned to treating the vaccine injured more or less exclusively. For more information, visit DrPierreKory.com. McCullough is also investigating additional post-jab treatments, which you can find on PeterMcCulloughMD.com. Finally, if you’re suffering from long vax, be sure to review my strategies for boosting mitochondrial health to allow your body to heal.

from:      https://articles.mercola.com/sites/articles/archive/2024/07/01/off-switch-covid-mrna-shots.aspx?ui=f460707c057231d228aac22d51b97f2a8dcffa7b857ec065e5a5bfbcfab498ac&sd=20211017&cid_source=dnl&cid_medium=email&cid_content=art1HL&cid=20240701&foDate=true&mid=DM1595025&rid=61761564