by Dr. Joseph Mercola, Mercola:
STORY AT-A-GLANCE
- Oncologists are reporting an alarming rise in post-jab “turbo cancers,” a term coined to describe incredibly rapid-growing cancers in people who have received one or more COVID jabs
- Turbo cancers are showing up in young people, many under the age of 30, with no family history of cancer. They’re also showing up in pregnant women and young children
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- Most turbo cancers are Stage 3 or 4 by the time they’re diagnosed, yet symptoms only arose days or weeks ago. They grow and spread so rapidly, many patients die before treatment can even begin. Most turbo cancers are also resistant to conventional treatment
- There are several possible mechanisms of the COVID shots that can lead to cancer in susceptible individuals. The primary one is the modification of the mRNA used. Pseudouridine was inserted to stabilize the RNA. The resulting protein can easily get misfolded, and protein misfolding is a hallmark of Alzheimer’s, Parkinson’s and heart failure
- The pseudouridine insertion can also suppress your innate immune surveillance by dampening the activity of toll-like receptors, and reduced cancer surveillance is a downstream effect of that
In a September 22, 2023, Highwire interview (video above), Canadian oncologist and cancer researcher Dr. William Makis discussed the alarming rise in post-jab “turbo cancers,” a term coined to describe incredibly rapid-growing cancers in people who have received one or more COVID jabs.
One example of this is detailed in a September 2023 case report1 co-written by Dr. Peter McCullough. It describes the rapid deterioration of a 56-year-old man who within days of his COVID shot developed Bell’s palsy, which progressed into an aggressive tumor on his ear and face. As noted in the abstract:2
“The malignancy was of cutaneous origin and the case showed symptoms consistent with Bell’s palsy and trigeminal neuralgia beginning four days post-vaccination … In this study we describe all aspects of this case and discuss possible causal links between the rapid emergence of this metastatic cancer and mRNA vaccination.
We place this within the context of multiple immune impairments potentially related to the mRNA injections that would be expected to potentiate more aggressive presentation and progression of cancer.
The type of malignancy we describe suggests a population risk for occurrence of a large variety of relatively common basaloid phenotype cancer cells, which may have the potential for metastatic disease. This can be avoidable with early diagnosis and adequate treatment.
Since facial paralysis/pain is one of the more common adverse neurological events following mRNA injection, careful inspection of cutaneous/soft tissue should be conducted to rule out malignancy.
An extensive literature review is carried out, in order to elucidate the toxicity of mRNA vaccination that may have led to the death of this patient. Preventive and precise routine clinical investigations can potentially avoid future mortalities.”
Another case report,3 published in November 2021, described the remarkably rapid progression of angioimmunoblastic T cell lymphoma in a 66-year-old man, mere days after he got his third Pfizer shot.
Ironically, he got the shot to protect him during chemotherapy, and in eight days, the cancer just exploded and spread like wildfire. According to Makis, that kind of progression would normally take a couple of years, or at most a few months.
Turbo Cancers — A New COVID Era Phenomenon
As noted by Makis, we’re now seeing the emergence of rapid-growing cancers of the breast, colon, esophagus, kidney, liver, pancreas, bile duct, brain, lung and blood — including exceedingly rare types of cancer.
But that’s not all. These cancers are showing up in young people, many under the age of 30, with no family history of cancer. They’re showing up in pregnant women and young children. Equally odd is the fact that most are Stage 3 or 4 by the time they’re diagnosed, yet symptoms only arose days or weeks ago.
The cancers grow and spread so rapidly, many of these patients die before treatment can even begin. Most of them are also resistant to conventional treatment and don’t respond. “I’ve never seen cancer behave like this,” Makis says, and he should know, having diagnosed 20,000 cancer patients in his career so far.
Makis first caught wind of this phenomenon when he started tracking the sudden deaths of Canadian doctors, who had to take the full battery of COVID shots to keep their jobs. Within months, there was a rash of sudden deaths among them, many due to heart attacks and dying in their sleep. But there was also a large group of doctors who developed aggressive cancers.
Makis points out that when you look at Go Fund Me pages asking for donations for cancer treatment, a large portion of these people are in professions that were mandated to take the shots, such as medical professionals and school teachers, police officers, fire fighters, military personnel and airline crews.
Potential Mechanisms of Action
When asked how the COVID shots might be causing these turbo cancers, Makis describes several possible mechanisms that can lead to cancer in susceptible individuals. The primary one is the modification of the mRNA used.
The COVID shots do not contain the identical mRNA found in the SARS-CoV-2 virus. The mRNA has been genetically manipulated in a process called “codon optimization,” where pseudouridine is inserted to stabilize the RNA and prevent rapid breakdown.4
The reason codon optimization was used is because it’s difficult to get your body to produce a given protein by injecting mRNA. Not only is it rapidly destroyed, but for the injection to work, they also need higher levels of protein expression than is naturally possible.
They bypassed this problem by making substitutions in the genetic instructions. You can swap out certain nucleotides (three nucleotides make up a codon) and still end up with the same protein in the end, but the increased efficiency comes at a terrible cost.
When substituting parts of the code in this way, the resulting protein can easily get misfolded, and this has been linked to a variety of chronic diseases,5 including Alzheimer’s, Parkinson’s disease and heart failure.6
As explained by Makis, the pseudouridine insertion can also suppress your innate immune surveillance by dampening the activity of toll-like receptors, and one downstream effect of that is reduced cancer surveillance.
Other possible mechanisms include:
•Genomic integration of the modified mRNA through reverse transcription, which might disrupt tumor suppressor genes.
•Genomic integration of DNA contaminants in the shots, which might disrupt tumor suppressor genes.
•Tumors may so be promoted by the presence of an SV40 promoter in the DNA contaminants.
•The liposomal nanoparticles (LNPs) spread the mRNA systemically, to all tissues, with severe impacts on your immune function. We now know that some individuals continue to produce spike protein for at least six months, and when your body is repeatedly (let alone continuously) exposed to the same antigen, it creates tolerance.
As a result, you become more prone to infection because your immune system no longer puts up a fight against the antigen. However, the same antibodies that target infections also target cancer cells, so your cancer risk goes up as well.
•Plasmid DNA can also be taken up by gut bacteria, causing them to become a source of constant antigen (spike protein) production.
