QUANTUM ENGINEERING #62: CENTRALIZED IDEAS ABOUT CANCER ARE 180 DEGREES FROM NATURE'S TRUTH

Tumor immunity represents a new avenue for cancer therapy. Immune checkpoint inhibitors have successfully improved outcomes in several tumor types. In addition, currently, immune cell-based therapy is also attracting significant attention. However, the clinical efficacy of these treatments requires further improvement. The mechanisms through which cancer cells escape the immune response must be identified and clarified. Cancer stem cells (CSCs) play a central role in multiple aspects of malignant tumors. CSCs can initiate tumors in partially immunocompromised mice, whereas non-CSCs fail to form tumors, suggesting that tumor initiation is a definitive function of CSCs. However, the fact that non-CSCs also initiate tumors in more highly immunocompromised mice suggests that the immune evasion property may be a more fundamental feature of CSCs rather than a tumor-initiating property.

What if stem cells' "evasion-by-replication" strategy were the root of cancer when they are hit by vaccine particles?

What If human cancer theory is upside-down?

In my Rubin Huberman podcast I told that it is upside based on the light story.  It turns out it is upside down because of the SV-40 story uncovered by Sarah Stewart in the Cutter Incident too.  How?

Cancer cells are actively looking for a source of UV light to control the cell cycle.  Cells migrate when Ulraweak UV biophotons are absent from mitochondrial metabolism.

You'll begin to see a new mitochondrial perspective of my advice.  Transfecting immuno privileged stem cells with SV-40 is a bad idea with horrible consequences.

COVID-vaccine-induced cancer data from the Ethical Skeptic demonstrate cancer genesis isn't necessarily a long inexplicable number of somatic mutations like Philip Buckholdts wants you to believe.  Cancer genesis is contamination-induced and electromagnetic radiation increases contamination by DNA destruction which act as plasmids. The Covid aftermarket data now suggests 1 in 225 shots could trigger cancers.

People forget each octave of the electromagnetic spectrum has a particular energy associated with it and that energy links to how DNA is damaged.  For example, DNA replication errors, especially those occurring at regions that are hard to replicate, are called fragile sites.  These sites can cause breaks in DNA that results in pieces and parts of nDNA. This process alone can lead to cancer, primarily by making it more likely that fragments of chromosomes rearrange themselves, activating genes that lead to uncontrollable cell division.  Mary Sherman and Sarah Stewart invented this science in their bio-weapons lab in New Orleans.

What is the target that these two women trip over with their use of the LINAC?

Cancers can be categorized into two groups: those whose frequency increases with age, and those resulting from errors during mammalian development. The first group is linked to DNA replication through the accumulation of genetic mutations that occur during proliferation of developmentally acquired stem cells that give rise to and maintain tissues and organs.

These mutations, which result from DNA replication errors as well as environmental insults, fall into two categories; cancer driver mutations that initiate carcinogenesis and genome destabilizing mutations that promote aneuploidy through excess genome duplication and chromatid missegregation. Increased genome instability results in accelerated clonal evolution leading to the appearance of more aggressive clones with increased drug resistance.

The second group of cancers, termed germ cell neoplasia, results from the mislocation of pluripotent stem cells during early development. During normal development, pluripotent stem cells that originate in early embryos give rise to all of the cell lineages in the embryo and adult, but when they mislocate to ectopic sites, they produce tumors. Light is capable of causing this mislocation.  This is a transgenerational effect of the electromagnetic spectrum.  The LINAC use showed this and that is why the SV-40 virus was made uber virulent by Sherman and Stewart work in New Orleans for the CIA.

Geminin is the target of the light spectrum in mammals to protect it from cancer.

Remarkably, pluripotent stem cells, like many cancer cells, depend on the Geminin protein to prevent excess DNA replication from triggering DNA damage-dependent apoptosis. Apoptosis is controlled by ultraweak UV light generation by mitochondrial metabolism.  This link between the control of DNA replication during early development and germ cell neoplasia reveals Geminin as the target of light.  Big pharma and oncology want to use geminin as a potential chemotherapeutic target in the eradication of cancer progenitor cells.  Light is better than drugs because it has no side effects. All drugs carry the side effect risks.  Oncology favors drugs because they are patentable for the profiteers they serve in centralized healthcare.

In centralized medicine & science there should be strict observation and questioning.  This is key to finding a solution to a problem.  They do not want to find a solution because it destroys the business model of oncology.

1. Observation: COVID vaccinations have already triggered many cancer, and a significant number of people have already died from cancer.
   Question: If supposedly viruses such as HPV trigger decades-long domino effect that leads to cancer, why do these vaccines accelerate it so much? Have we got it all wrong?
2. Observation: The mechanism of action of COVID vaccines is to penetrate a cell, hack it, have it produce a protein to trigger antibodies, but also to trigger a T-cell attack on the contaminated cell.
   Question: How come normal cells have survived that vaccine contamination and morphed so quickly into a cancerous cell?
3. Observation: When you dive into vaccine-induced case reports, you realize most vaccines are capable of triggering cancer.
   Question: How and why do different vaccine technologies, targeting different viruses or bacteria, all end up having the same effect? Isn’t there another more automatic process at play?

Cancerous cells have very distinct features that cannot be regained by normal cells over night. And the idea that any push genetic in any direction, would always end up with the same outcome is genetically or mathematically impossible.

So, what’s going on?

Centralized science in cancer believes the following:  The majority of cancers result from random mutations arising during DNA replication in the normal stem cells required during development and tissue maintenance. Differences in cancer risk among different tissues can be explained by the total number of stem cell divisions in those tissues.  Is this true based on the Covid data?  It is not.

That means something else is behind the numbers.  What is it?

SV-40 and the light you live in.

SUMMARY

Mammalian cancer cannot start in normal cells penetrated by vaccine particles, because  these cells will be destroyed by the immune system MHC complex.  The human immune system is highly efficient at clearing cancer cells via this mechanism. In humans, cancer can only be started in stem cell which are normally immune protected. So human cancer cells always have all the traits of a stem cell. That is not what centralized oncology believes.  What a coincidence? Cancer theory was always upside down.  And none of them knew that ultraweak UV bio-photons stimulate mitosis to get a stem cell out of normal immune protection. That implies UV light is the best chemotherapy one can have.  It also means it is the best therapy to use in vaccine induced cancer and injury like long COVID.