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By October 2022, there was a significant increase in fourteen different types of cancers across 44 countries, particularly among young people.

The American Cancer Society reported that cancer mortality in young people had doubled compared to pre-2020 levels.

Pfizer’s 2022 safety report on covid “vaccines” documented thousands of cancer cases following vaccinations, with 3,711 cases reported by June 2022.

UK oncologist Angus Dalgleish observed aggressive cancer relapses in patients who had received covid booster vaccines, suggesting a link between the vaccines and cancer.

Canadian oncologist William Makis noted unprecedented cases of stage four cancers in young adults, describing them as “turbo cancer” due to their aggressive nature and resistance to conventional treatments.

Pathologist Ryan Cole criticised covid injections for causing immune suppression, which impairs the body’s ability to fight cancer, and reported a significant increase in cancer cases post-vaccine rollout.  Cole estimated that 17 million people have died due to mRNA injections, describing the situation as a “silent holocaust” and criticising the medical establishment for denying these deaths.

“It is important to fully appreciate the spike protein burden in the vaccinated, in order to be able to find the best strategies to reverse the risk and the damage of this toxin … The better we understand these processes, the better we will be able to defend patients and the public against the imminent coming years of record-breaking cancer rates,” Dr. Coleen Huber wrote in a recent essay.

Over the years, The Exposé has frequently published articles about the risk of vaccine-induced cancers and the increase in cancer cases after the mass rollout of the covid so-called vaccines.  But many may have missed all the pieces in the puzzle, especially if they have not been following the real news as it was breaking.  Thankfully, Dr. Huber has gathered all the evidence into one essay for us which we have reproduced below.  In her essay, Dr. Huber explains:

– The mechanism of mRNA “vaccines” and the resulting spike protein production by people’s bodies after vaccination.

– The correlation between covid injections and certain cancers including lymphomas, glioblastomas, colorectal, ovarian and breast cancers.

– The global rise in cancer cases and mortality post-vaccination.  Globally, cancer diagnoses and excess deaths have risen following the covid vaccine rollout, with a notable acceleration after booster doses, particularly affecting younger age groups.  “The vulnerability is sufficient for all humans to be sure to avoid the covid vaccines,” Dr. Huber writes.

– The concerns and cautionary advice regarding vaccination for cancer patients.  People, who already face cancer as a leading cause of death, should avoid covid injections.

– The impact of covid injections on immune response and antibody production and the role of Type I interferon in immune function and cancer suppression.

– The mechanisms of cancer development and the role of spike protein.

– The impact of spike protein on DNA damage and repair.

– The suppression of tumour suppressor genes by spike protein.

– The spike protein’s role in cancer growth and angiogenesis.

– The immune evasion by cancer cells and the impact of vaccination.  The covid injections may weaken the immune system and allow cancer cells to evade immune detection.  Tumours can evade the immune system by disguising themselves as “self,” making it difficult for the immune system to target them.

– Enhancing immune vigilance and the role of vitamin A.  Vitamin A has been shown to help unmask hidden cancers, allowing the immune system to target them, and its deficiency is linked to camouflaged colorectal cancer.

– Metastasis, the spread of cancer cells to new locations in the body, and the importance of basement membrane integrity.

– The DNA contamination in covid injections (dubbed PlasmidGate) and its potential risks.

– N1-Methyl-pseudouridine, used in the mRNA of covid injections to stabilise the Spike Protein for immune recognition, and its potential link to cancer.  Other potential cancer risks from covid injections include contamination with the oncogenic SV40 virus, the presence of CD147 in the spike protein and microclots induced by spike proteins.

– Ivermectin as a Potential Treatment for covid and cancer.  Ivermectin has shown effectiveness against the spike protein, which is the main toxin in both covid infection and its vaccines.  Studies have shown that ivermectin can reduce tumours by 50% to 85% in cancers such as glioblastomas, colon and breast cancer, and it has shown effectiveness against a wider range of cancers in vitro.  Ivermectin was found to outperform the standard chemotherapy drug gemcitabine in treating pancreatic cancer.

Covid Shot-Cancer Links; Understand Them To Defeat Them

By Dr. Coleen Huber

Table of Contents

PART 1:  Statement of the Problem

By October 2022, mainstream media could no longer ignore the enormous rise in fourteen different types of cancers in 44 countries around the world and most remarkably in young people. ^{[1] [2] [3]}  The American Cancer Society acknowledged that cancer mortality has doubled in young people from pre-2020 levels. ^[4] Pfizer’s 2022 safety report on the covid-vaccines revealed thousands of cancers of hundreds of types following the injections. ^[5]  By June 2022, there were 3,711 cases reported by Pfizer under that heading.

Oncologists Note Stark Difference In Cancers From Pre-2020 To The Present

UK clinical oncologist Angus Dalgleish, one of the leading oncology researchers in the United Kingdom, sees an alarming number of cancer patients, long in remission, who “ … subsequently present with very aggressive relapse when they should have stayed in remission.  Sadly, I have yet to find a case where the patients have not received a covid booster vaccine from their GP or hospital because they are ‘at risk’.” ^[6]  His comment on cancer mortality developments around the world is that “the covid vaccines are linked to cancer and death.” ^[7] 

Canadian oncologist William Makis MD, who has diagnosed over 20,000 cancer patients over his career, says, “I’ve never seen anything like this … I’ve never seen stage four breast cancers presenting in women in their twenties.  I’ve never seen stage four colon cancers presenting in men and women in their twenties and thirties … These cancers would always present at stage four, and they would always kill them in a matter of a few months, and it was always less than a year … ‘Turbo cancer’ is a term that people came up with to describe the extremely aggressive nature of these cancers in the covid vaccinated, and these cancers behave extremely differently, unlike anything I’ve seen before in my career … And the other feature of these cancers is that they are very resistant to conventional treatment; they’re resistant to radiation therapy, they’re resistant to chemotherapy, and patients seem to be doing very poorly with conventional treatments.  Oncologists are really baffled, and they don’t know what to do.“ ^[8]

Pathologist Ryan Cole MD, formerly of Mayo Clinic, specialises in postmortem examination.  He has criticised covid vaccines for, among other dangers, the severe impairment of the immune system and impairment of the ability to fight cancer.  He says “People ask, ‘Do these shots cause cancer?’  Well, they cause immune suppression. They cause a disruption and a dysregulation of your immune system that is normally what would fight cancer.  So that’s what we’re up against … As I travel the world and talk to doctors … they are seeing cancers in age groups they have never seen before, and it happened after the rollout of the [covid injections]  … In 2021, there was about a 6% or 7% increase in cancer.  In 2022, there was a 35% increase above average in cancer … People who have been clear of their cancer, 2, 3, 5, 10 and even 20 years, where, after the shots, their cancer aggressively came back, and the estimates are of 17 million people who have died of these mRNA injections … This is a silent holocaust, and that’s what’s sad about this.  People were coerced into an experiment, and the deaths are being denied by the medical establishment.” ^[9]

Spike Protein Dosing From Pfizer and Moderna

The amount of mRNA dose in each Pfizer vaccine is 13 trillion mRNA molecules, and in Moderna is 40 trillion molecules, each enveloped in its own cationic lipid nanoparticle.  These figures were determined by molecular weight of each of the two vaccines. ^[10]  To put those numbers in perspective, there are about 30 trillion cells in the human body.  So, one can imagine the impact of a maximally ubiquitous distribution throughout the whole body, in a roughly one-to-one or one-to-three ratio of payload unit to human cell. 

Each of those two vaccines encoded whole spike proteins and each of the trillions of lipid nanoparticle (“LNP”) enveloped mRNA codes for spike protein. ^[11]

The Pfizer vaccine was not studied for carcinogenicity or genotoxicity (DNA damage potential) by Pfizer prior to rollout, as we can see from Pfizer’s own documentation to the FDA: ^[12]

From very early on in the covid vaccine heyday, February 2021, there was already evidence that covid vaccines produced a vastly higher spike protein burden in the vaccinated people than after natural infection.  Even within three weeks post-vaccination, the antibodies to spike proteins measured up to 100 times higher in the covid-vaccinated than in the unvaccinated and previously covid-infected. ^[13]  While some may interpret these antibodies as a sign of a more intense immune response to spike protein, it also indicates a larger and/or more impactful presence in the body of this known toxin.

Therefore, it is important to fully appreciate the spike protein burden in the vaccinated, in order to be able to find the best strategies to reverse the risk and the damage of this toxin.  Toward this end, this article explores the mechanisms of cancer risk from the spike protein.  The better we understand these processes, the better we will be able to defend patients and the public against the imminent coming years of record-breaking cancer rates.

It should be noted that the spike protein rarely appears intact more than 20 days after covid virus infection, but the recombinant, that is, vaccine-generated, spike protein has been observed in the covid vaccinated, from 69 to 187 days following vaccination.  ^[14]  That particular study stopped at 187 days, rather than being the point at which no more spike protein was observed, which implies that there may be a longer time period of spike presence in the bodies of vaccinated people.  This persistence includes both the injected mRNA enveloped in liposomes as well as its derivative spike protein. ^[15]  This is plenty of time for the initiation of cancer-promoting pathways, and the inhibition of immune defences against cancer to begin.  And it is certainly enough time for cardiovascular and heart damage to have begun, as well as breach of the blood-brain barrier, as I discuss in other papers.  Peak uptake throughout the northern hemisphere was in the spring of 2021.  So that is quite a long time for spike protein to persist in the bodies of vaccinated people, whereas the fragile mRNA that initiated such spike protein production degrades in weeks, after the payload has been delivered.

Epidemiology of Cancer Risk Following the Covid Vaccines

covid vaccines are correlated with increased incidence of the following cancers.

Lymphomas are so closely correlated with mRNA injection that 45.7% of the studied lymphoma patients who were covid-vaccinated developed lymphoma within only 30 days post-injection, rather than later. ^[16]  It is not surprising that this is one of the main cancers seen post-covid vaccine because the T and B cells of the lymphatic system are not only quickly reproducing, but as waste-drainers, lymph nodes are among the earliest of the body’s tissues to take up spike proteins.

Glioblastomas are pernicious cancers due to their easy accessibility to surrounding brain tissue, and their shielding from most potential treatments behind the blood-brain barrier, among other challenges.  Pfizer reported hundreds of brain cancers and pre-cancerous conditions in their June 2022 update. ^[17]  Reduced Cytochrome C levels were found in glioma patients post-covid vaccine, which seemed to be due to impaired oxidative phosphorylation and consequent lower ATP in the mitochondria. ^[18]

Ovarian and breast cancers are also seen with increased incidence since covid vaccine rollout, probably due to their p53 impact, yet the covid vaccines have damaged this p53 gene, the “guardian of the genome” protector of DNA, which I discuss below.

Colorectal cancers have proliferated, and aggressively and among unprecedented young ages since the covid vaccines.  William Dahut is the chief scientific officer of the American Cancer Society.  He says, “Colorectal cancer are also presenting with more aggressive disease and larger tumours at diagnosis; it’s more difficult to treat.”   Regarding this steep increase in colorectal cancer in youth, Harvard medical professor Kimmie Ng comments that “the steepest rises are in the very youngest people, those in their 20s and 30s.” ^[19]

Although the above are some of the most prominently increased cancers, there is no type of common cancer that has been observed to stay flat in incidence since the rollout of the covid vaccines. All have been listed in the Pfizer documentation. ^[20]

The Vaccine Adverse Events Reporting System (“VAERS”), which is overseen by the US Centres for Disease Control (“CDC”) and the Food and Drug Administration (“FDA”), is a national surveillance system regarding adverse vaccine effects, for all vaccines given in the US, including the mRNA covid vaccines.  For all of the entries regarding cancers in the year 2021, the researchers found that 96% of all the entries for any of the search terms related to cancer were specific to the covid vaccines, and only 4% for all the other kinds of vaccines put together. ^[21]

Worldwide, cancer diagnoses and total excess deaths began to rise following the rollout of covid vaccines, and then to accelerate following the boosters.  The findings are most remarkable in younger ages than are typically affected by cancer. ^[22]

CDC data on cancer mortality summarised below by The Ethical Skeptic shows a sharp inflection point in vastly increased cancer mortality (those with cancer listed as the cause of death) in the United States beginning right at the time of the covid vaccines rollout, the last week of December 2020.  In the following graph of cancer mortality in 0 to 54-year-olds, the inflection point of when cancer began to increase beyond yearly averages is quite clear, beginning the week after 14 December 2020, when the vaccine first became available. ^[23]  Because this graph shows deviation from the trend rather than actual numbers, the curve is often below zero through 2018 – 2020, as cancer mortality was somewhat lower than prior rates then.  My other observation is that the first spike after the vaccine rollout likely reflects those who already had fulminant cancer, now worsened by the toxicity of the vaccines, in which case, cancer would have been the default cause of death listed on the death certificate.  However, the continuing trend upward of the cancer mortality trend from 2021 to the present is a very strong indicator that a nationwide health-impact event in late 2020-early 2021 caused that sharp increase, and for that we know of only one.  All of the following data is derived from CDC-reported data.

An enormous study of the entire Japanese population from national vital statistics showed that excess mortality was seen for all cancers examined, 20 types of cancer, each with over 95 or 99% of PI since the rollout of the covid vaccines. ^[24]  The paper’s politically incorrect findings, based on uncomfortable data, earned its retraction by the journal Cureus.  At least 80% of the Japanese population had had two doses of mRNA vaccines and 68% of the population had received a third dose.  In that study of the Japanese population, the main cancers to increase following the covid vaccine rollout were ovarian cancer, leukaemia, prostate, lip / oral / pharynx and pancreatic cancers.  Breast cancers dipped lower at first, and then shifted to excess mortality also, though the last without statistical significance.

Skyrocketing cases of cancer in the UK have been attributed to smoking, ^[25] although smoking has drastically decreased in the UK in recent decades, as in the rest of the world.  Thirteen new cancers are now being attributed to smoking by the corporate media, which is highly improbable.

Cancer’s attacks on the body are multi-faceted.  They are so complex that researchers Valdes and Perea write:  “This staggering intricacy [of cancer’s many effects] calls for caution when advising all people with cancer (or a previous history of cancer) to receive the covid-19 primary vaccine series plus additional booster doses.” ^[26]

To this I would add:  Are you a member of a species, such as humans, in which cancer was already the first or second cause of death every year before the covid vaccines?  In that case, the vulnerability is sufficient for allhumans to be sure to avoid the covid vaccines, as I will show in detail below.

PART 2: Mechanisms by Which the Covid Vaccines Induce Cancer and Natural Therapies That Reverse These

IgG4 is an antibody made in abundance by covid-vaccinated persons, many times higher than in the unvaccinated. ^[27] Antibodies such as the IgG type immunoglobulins are easy to test for by a blood lab, and they are easy to understand.  When some irritant – either a pathogenic microbe or allergen – enters the body, then we make reactive antibodies as newly generated soldier molecules to fight the intruders.  This is the role of the B-cell-generated immunoglobulin antibodies.  So, when researchers discovered the huge disparity between the covid vaccinated and the unvaccinated in IgG4 counts, people got excited, and journalists wrote of the stark discovery.

IgG4 is thought to be associated with tolerance of invading microbes, and it is thought that this distracts or shifts the focus of immune system surveillance away from the more inflammatory, combative, so to speak IgG1 and IgG3, and thereby away from important battles against invading pathogens or even cancer.  And IgG4 is specifically more tolerant of the SARS-CoV-2 spike protein among other proteins and microbes that do not belong in the body, and that this complacent immune reaction to the spike protein can promote infection and replication by SARS-CoV-2 without opposition. ^[28]

But there is a problem with all those assumptions and all that attention.  IgG4 is a downstream effect, and a product of a vanishingly small component of immune system cells, that is a small fraction of the molecules made by B cells, which comprise only 0.005% = five of every 100,000 blood cells.

That is, IgG4 is unlikely to have as much effect on covid risk, other microbial risk or cancer risk.  But it may serve as a convenient marker on blood labs that gives clues of underlying immune system battles of more importance.

Rather, the most important discovery on covid vaccine-induced cancer risk is something completely different, which is the loss of Type I interferon, and the loss of interferon signalling, in the covid-vaccinated, which is a tragic loss of many downstream immune functions against cancer.  The difference in the importance of these two phenomena is that IgG4 is very rare and very far downstream, while Type I interferon is centrally coordinating of the entire immune system, ubiquitous in healthy people, and significantly reduced in the covid vaccinated.  And this is the central immunity injury that the covid-vaccinated are faced with.  Both of these phenomena are concerning to UK clinical oncologist Angus Dalgleish, who was co-discoverer of the CD-4 receptor.  While speaking with US Senator Ron Johnson, Dr. Dalgleish shares his concerns regarding the covid vaccines, with regard to cancer, is that the covid vaccine boosters suppress the immune system’s T-cell response, and immunoglobulins switched to tolerisation, as two mechanisms most concerning to him by which the covid vaccines induce or worsen cancer. ^[29]  The Pfizer covid vaccine specifically was found to significantly reduce Type I interferon, also known as interferon alpha. ^[30] This causes a tremendous downstream effect of multiple pathologies, both infectious disease and malignant cancer.

Type I interferon, the body’s most important cytokine, is not to be underestimated for its effect against cancer, and this is due to an enormous array of anti-cancer effects.  Some of those effects are arrest of the cell cycle, apoptosis, or natural cell death, as well as stimulation of our greatest warriors against cancer, namely the natural killer cells and the CD8+ cytotoxic (“killer”) T-cells.  So, when covid-vaccinated people display sharply reduced Type I interferon, compared with the unvaccinated, this is a staggering level of vulnerability with respect to cancer.

One of those very important functions is G-quadruplex influence over Type I interferon, which in turn affects transcript, replication and genomic stability.  The Seneff research team gets deep into the details of these mechanisms, ^[31] beyond the scope of this paper, and well worth studying as theirs is the most important analysis to date of the enormity of the covid vaccine assault on overall immune function.

Cancer Attacks the Body in Seven Major Ways

At the turn of the millennium, Hanahan and Weinberg identified six major “capabilities” of cancer to undergo changes to promote its own growth and immortality. ^[32] John Boik summarised the seven major categories of attack inflicted by cancer against the body. ^[33]  I discuss those peculiar features of cancer here, and the roles of vitamins D, C and A against most of those routes of attack. ^[34]  Those are damage or destabilisation of DNA, and resulting abnormality in gene expression, abnormal cell signalling and other cell-to-cell communication; angiogenesis, which is the formation of new blood vessels to feed a tumour; invasion and metastasis; as well as immune evasion/camouflage. 

I will show throughout this paper that the spike protein carries out most of these functions, in promotion of cancer, and to the detriment of the person with a cancer risk or a cancer burden.

Let’s look at DNA damage first.

Spike Proteins Damage DNA, and That Is A Major Cancer Risk

When DNA is damaged, cancer is a risk. ^[35] Perhaps the most important cancer risk from the covid vaccines is damage to DNA.  The spike protein has been found by Jiang et al to localise to the cell nucleus, where they were found in abundance and to significantly damage DNA and to alter pathways for DNA repair. The cells most abundant in spike proteins showed the most DNA damage, including the DNA in T-cells and B-cells, showing impairment from this damage. ^[36]  The tragic effect of this is that when spike protein hangs around cells long enough, such as with the mRNA perpetually regenerated spike proteins, your cells’ protective mechanisms against cancer would come to a stop.  Not surprisingly, given the current political climate, and despite Jiang and Mei’s meticulously reported data, the Viruses journal retracted their paper, and those who retracted it had financial ties to both Moderna and Pfizer. ^[37]   What Jiang and Mei had proven was what pundits denied, but what Pfizer documentation had already proven: that the spike proteins do enter human cells, and cell nuclei, and do affect DNA.

The SARS-CoV-2 spike protein has been found to cause cells to fuse together to form syncytia, which are multi-nucleated, like cancer cells.  And this process has been known to cause cancer. ^[38]  This leads to aneuploidy in daughter cells, which is carcinogenic. Aneuploidy is a different number of chromosomes than the normal 46, either excess or deficient.  So, DNA is damaged in this way as well, on exposure to spike proteins. ^[39]

The problem is that DNA repair is essential for B and T cell immunity; it is the core of that adaptive immune system’s ability to defend the organism from both cancerous and infectious disease, ^[40] and DNA repair is essential to achieve the versatility needed by that adaptive immune system to be able to protect the person from the variety of infectious and cancerous assaults that each of us faces over the course of life. Indeed, these processes are so fundamental to capable immune surveillance that they are necessary for that ubiquitous and even omniscient monitoring ability of the immune system.  Both developing and mature B and T cells, as all cells, need to break and then to repair DNA in order to diversify and to be able to achieve the versatility to accomplish this difficult task.^[41] [42]  But the spike proteins interfere with this highly complex, evolution-trained and essential immune function.  All of these sub-cellular activities are highly organised.  Spike proteins throw a kind of microscopic shrapnel into that exquisite system.  The damage is so great that Pfizer scientists found that covid vaccine-injected people showed lymphocytopenia (lack of T and B cells) measured two weeks after injection of their second dose.  [43]

Cell Signalling Shutdown, With Auto-Stimulation and Immortality

That was a general view of the damage to DNA from spike protein.  Here are some of the specific genetic downstream effects from that damage.

Vaccine developers placed higher guanine-cytosine content in the covid vaccine RNA than is present in either the wild SARS-CoV-2 virus or in human RNA.  These tend to stack into dense formations of guanine bases, which form G-quadruplexes (four guanines stacked together).  In excess, this has been found to have downstream effects of dysregulating the G4-protein binding system, which among other diseases, has been found to lead to malignant cancers, by dysregulating human RNA. ^[44] [45]

The spike protein was found to suppress a p53-dependent gene, leading to tumorigenesis.  P53 has been named the “guardian of the genome,” because its well-appreciated function is to prevent cells that have mutated or damaged DNA from reproducing.  Of all the body’s proteins, p53 is the most effective suppressor of tumours.  P53 accomplishes this by influencing a large set of genes that carry out a variety of functions against cancer. ^[46] The three major functions of p53 are to stop growth, to repair DNA and to make sure that a cell dies a normal cell death at the end of its life, rather than gain immortality as cancer cells do. ^[47]  Loss of p53 removes these protective effects for the individual against rampant cancer growth, and nearly half of tumours contain mutated p53. ^[48]  Cancer cells that had high amounts of spike proteins had reduced p53 signalling and reduced p53 transcriptional activity, and after this damage, no controls on cancer cell multiplication were observed. ^[49] In this way, spike proteins removed an important protective feature against cancer, and then the brakes were released, so to speak, on the proliferation of cancer cells.   

Of concern in breast cancer is that the spike protein interacts with BRCA, which is a long-recognized tumour suppressor protein.  That protein regulates genes that have effects against cancer. ^[50]  Cancers of the breast, uterus, ovaries and prostate are associated with altered BRCA1 activity.  BRCA2 mutations are primarily correlated with cancers of the prostate, pancreas as well as melanoma. 

Nuclear factor-kappa B (NFκB) is the name of a group of proteins that cause cancer cells to grow and multiply while lending them immortality, which makes them a threat to surrounding organs.  Spike proteins were found to stimulate and to grow lung cancer by using this NFκB pathway. ^[51]

Angiogenesis

The NFκB proteins discussed in the previous paragraph create another problem that strengthens cancer to the detriment of the person, and that is that NFκB stimulates angiogenesis, ^[52] which is the formation of new blood vessels in the vicinity of the tumour; this is thought to be due to the tumour’s fast-paced metabolism demanding sugar and other fuels, as well as the blood vessel super-highways to satisfy all that demand for fuel, so to speak.

Copper is an essential micronutrient, but must be limited, because of its role in angiogenesis, which has been known since the 1960s. ^[53]  My clinic has long incorporated zinc in our treatments for cancer, and we have tried to limit copper as much as possible to not stimulate angiogenesis, or to act as an obstacle to it.  Zinc is a natural rival opponent of copper.

Immune System Evasion

Two issues arise with immune system effects of the covid vaccines.  That is, there is a weakening of the immune system, and there is camouflage or evasion of the immune system by the cancer.  Tumours have several mechanisms of camouflage or evasion of targeting by the immune system. ^[54]  The problem is that our immune systems exist to seek and destroy that which is “non-self,” and tumours disguise themselves, in their antigen display and antigen concealment, as “self.”

Covid vaccination led to a loss of Type I interferon, which is the immune system’s most important non-nutrient biochemical, which initiates a necessary cascade of immune responses in the event of a pathogenic or cancerous attack.  As a result, there are downstream disturbances and failures in the regulation of cancer surveillance. ^[55] 

This leads to increased PD-L1 protein expression on cells, which gives cancer a refuge from immune system surveillance, ^[56] and functions as a distraction to the immune system with regard to cancer.  The PD-L1 protein makes it so that cancer is not apprehended by cells of the immune system, due in part to the distraction of spike protein assault, as an invading pathogen that itself must be fought.  The PD-L1 protein has been found to be significantly increased in covid-vaccinated people. ^[57] 

However, the other half of the immune system evasion resulting from decreased Type I interferon is this:   The immune system, under the influence of Type I interferon, and then major histocompatibility complex (MHC) class 1 antigen displayed on cancer cells, earmarks and targets cancer cells for the immune system to destroy them. ^[58] But alas, with the loss of type I interferon, there is a consequent loss of MHC antigen presentation by cancer cells, and thus cancer cells escape the immune system undetected.  

The direct effects of Type I interferon against cancer include the above functions plus the following:  the arrest of the cell cycle (checking rampant growth), tendency toward differentiation (which is a benign rather than a malignant development), initiation of apoptosis (normal “on-time” cell death rather than cell immortality), stimulation of natural killer (“NK”) cells and cancer-killing (CD8+) T-cells activity. ^[59]

Also, inactivated covid vaccines have been correlated with the loss of the very important CD8+ T-cells. ^[60]  As Ryan Cole MD describes this problem, the covid vaccines “put your T-cells to sleep, in a manner that they can’t fight … because those T-cells have gone to sleep to a degree that they would normally fight off cancer, and now they’re not there to fight off cancer.” ^[61]  This also appears to be due to loss of Type I interferon.

In my work with cancer patients over the years, it has been an essential part of our work to keep the immune system vigilant to the presence of cancer and reactive against it.  This is very difficult to achieve pharmaceutically, because unlike an obviously foreign item such as a virus or pathogenic bacteria, cancer cells appear to be “self,” and are then too often tolerated without opposition by the immune system.  So, there is not likely to be a synthetic substance that can accomplish that enhancement of immune vigilance.  Vaccines, despite their three-century history, have never achieved such a feat.

Vitamin A, on the other hand, has been able to unmask, so to speak, previously hidden cancers from the immune system, and allow those cancer cells and tumours to be targeted for destruction.  On the other hand, it has been found that when vitamin A is deficient, colorectal cancer remained camouflaged from the immune system. ^[62]  This likely has been due primarily to vitamin A’s suppression of the pro-cancerous interleukin IL-6. ^[63]  

The topic of IL-6 bears examination because there is evidence that CD-147, which is abundant on the spike protein, promotes TNF-alpha, which is highly carcinogenic, and that in turn strongly promotes IL-6. ^[64]

Vitamin A has been able to fight cancer on a number of molecular and cellular levels, beyond the scope of this discussion, ^[65]  but its usefulness against IL-6 alone has been worthwhile. For this reason, vitamin A has been an ever-present part of the cancer treatment protocols at our clinic since 2006, and at far higher doses than are discussed by the FDA.  I have often discussed anywhere from 50,000 to 300,000 units per day with patients, depending on the person and the aspects of their particular cancer.  The success of our clinic’s results against cancer is likely due not to any one of the treatments that we use, but to the synergy among well-tolerated and compatible nutrients that have complementary anti-cancer effects.

Metastasis: An Invasion of Tumours at Sites Near and Far From the Primary Tumour

When matched with an unexposed control group, the SARS-CoV-2 spike protein was found to stimulate the migration of lung cancer cells through the blood, and subsequent invasion of the basement membrane in a new location in the body. ^[66] That process is known as metastasis.  Not only do cancer cells break off from a primary tumour to then travel in the bloodstream, but weak basement membranes of different bodily organs are fertile ground for a new secondary tumour to gain a foothold.  Think of this as, for example, an old ceramic coffee cup with a scratched surface in one area.  That area is where the coffee will seep into and stain more so than the resilient finish of the rest of the cup.  Similarly, the basement membranes that protect our cells are most vulnerable to a new metastasising cancer cell floating by in the blood at that weak area rather than where the basement membrane is intact and thereby more resilient to such penetration.

My clinic, since 2006, has fought against basement membrane weakness and friability; that is, our clinic has worked to strengthen our cancer patients’ basement membrane resilience against metastatic invasion.  Vitamin C is a necessity, not a luxury, for building collagen, which I describe to patients as the equivalent of the bricks and mortar that we are made of, because collagen is by far the most abundant of the proteins in the body.  This is never recognised as the reason for vitamin C’s good effect against cancer, but I think it is one of the most important of its mechanisms.  There are dozens of types of collagens.  Pro-collagen requires vitamin C together with the amino acids lysine and proline.  Therefore, we prepare IV nutrient treatments for cancer patients that include these three ingredients.

Other Mechanisms of the Covid Vaccines That Promote Cancer

The above mechanisms of the covid vaccines against cancer are those with the most available evidence, and historically established as known cancer-promoting pathways.  However, there is also accumulating evidence of additional cancer-causing factors that are new and peculiar to these novel injections.

DNA plasmid contamination of the covid vaccines

Foreign DNA, which derives from amplification in the bacteria E. coli, contaminates both the Pfizer and Moderna vaccines.  This is a different but related problem than the problem of damage to human DNA that I describe above.

Dr. Phillip Buckhaults is a cancer genomics expert.  He testified, in a video that is no longer viewable on YouTube, to the South Carolina Senate on this DNA contamination found in covid vaccines.  He testified:  “The Pfizer vaccine is contaminated with DNA.  It’s not just mRNA.  I’m kind of alarmed about the possible consequences of this … It could be causing some of the rare but serious side effects like death from cardiac arrest.  This DNA can and likely will integrate into the genomic DNA of cells that got transfected with the vaccine mix.  It’s different from RNA because it can be permanent.  It could cause theoretically a sustained autoimmune attack toward that tissue.  It’s also a very real theoretical risk of future cancer in some people.   There’s probably about 200 billion pieces of this plasmid DNA in each dose of the vaccine . . . This is a bad idea.” ^[67]

Kevin McKernan was the first to discover and to write about this problem of plasmid DNA contamination of the covid vaccines. ^[68]  This was confirmed by Speicher and Rose. [69]

“Why does that matter?” asks pathologist Ryan Cole.  “That matters because that [E coli derived plasmid] DNA can park itself in the nucleus of your cell next to your own DNA, and piggy-back a ride into the next generation of cell, into the next generation of cell, etc. So, can it become part of the next generation that’s born?  It could … And this did happen in mouse studies up to four litters of mice.” ^[70]

Methyl-pseudouridine

N1-Methyl-pseudouridine (M1Ψ) was inserted into the manufactured mRNA used in the covid vaccines, which produced a genetically modified RNA, in order to stabilise the spike protein long enough to display it to the immune system, for recognition as a foreign antigen, so that the immune system could make antibodies against the spike proteins.  However, this creates new problems, including for cancer risk.  It turned out that the M1Ψ actually stimulated both cancer growth and metastasis in melanoma. ^[71]  Nevertheless, N1-methyl pseudouridine is naturally occurring in human RNA, comprising 1.4% of all bases in our RNA, and is necessary for our protein synthesis. ^[72]  So I doubt that this is a major cause of cancer, except by the indirect route of giving shelter from immune attack to spike protein production.

Other possible mechanisms of the increased rates of cancer being seen are an alleged contamination of the covid vaccines by the oncogenic SV40 virus, the CD147 presence in the spike protein favouring the carcinogenic TNF-alpha, ^[73] as well as possible contribution to cancerous processes by microclots induced by the spike proteins.

PART 3: Ivermectin’s Roles Against Covid Vaccine-Induced Cancers

Ivermectin is one of the safest drugs in existence.  Prior to the covid era, four billion doses had been given around the world in the half-century since its discovery, mostly in equatorial Africa, as ivermectin has excellent effects against tropical parasites.  However, it has been crucially important in the covid era, because spike protein is the main toxin in both naturally acquired covid infection as well as in the covid vaccines.  In the latter case, those full-length spike proteins are produced by the mRNA template.  I cited studies back in 2021, in my book ‘The Defeat of covid’, in which several teams of researchers had each shown that ivermectin effectively blocks the troublesome ends of the spike protein, both S1 moieties as well as S2, and that humanity would be fortunate if ivermectin blocked even one of those, let alone the much better effect of blocking all three.

Since that time, many more effects of ivermectin against spike protein have been found.  Clinical oncologist William Makis MD summarises fifteen of those. ^[74]

Essentially, ivermectin is able to not only block most of the worst effects of the mRNA vaccines, but it inhibits tumour growth and arrests the cell cycle of cancer, and in the very well-tolerated dose of 2 mg/kg body weight, which is roughly 136 mg dosing for a 150-lb person or 182 mg for a 200-lb person, and is compatible with both conventional chemotherapy as well as nutritional cancer therapies.

Remarkably, ivermectin was shown to oppose cancer stem cells. ^[75]  Those stem cells are what enable cancer to grow and later to recur.  I say that it is remarkable because previously, only vitamin C had been known to kill cancer stem cells, ^[76] [77] while being harmless to normal cells. ^[78]

Even at lower doses, studies summarised in the Makis paper have shown tumour reductions of 50% to 85% in some of the most devastating cancers caused by the covid vaccines, namely glioblastomas, and cancers of the colon and breast.  In vitro studies found ivermectin’s effect against a wider range of cancers, including the aforementioned, as well as pancreatic, ovarian, prostate and melanoma.

Regarding pancreatic cancer, ivermectin was found to be compatible with, and to outperform, the standard pancreatic chemotherapy drug gemcitabine, in its effect against that cancer. ^[79]

(I look forward to observing more and writing more as time goes on about the life-saving effects of ivermectin and other harmless interventions against not only covid but against the most common cancers of our time, especially those that have proliferated since the rollout of the covid vaccines.)

Endnotes

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About the Author

Colleen Huber is a Naturopathic Medical Doctor (NMD) in Arizona, USA, with expertise in vaccine safety concerns and events. She has served as a medical expert witness in court cases related to vaccine safety. Huber is also a Naturopathic Oncologist, holding a fellowship with the Naturopathic Oncology Research Institute.

Her clinic, Nature Works Best Cancer Clinic, had the most successful results of any clinic in the world reporting its results. She has served as the President of the Naturopathic Cancer Society, whose primary aim is to inform the public of safe and effective natural treatments for numerous types of cancer.

Dr. Huber’s book, ‘The Defeat of covid: 500+ medical studies show what works & what doesn’t’, presents a thorough examination of successful measures against covid-19. Written for a broadly educated layperson, the book is backed by over 500 medical and scientific endnotes.