Understanding your cancer risk with COVID vaccination

it is critical to note that none of the information provided here constitutes medical advice. The content presented is intended for educational purposes only. No claims regarding treatment outcomes or specific recommendations are made outside the context of documented clinical use of various compounds and therapies. Always consult with a nutritionally informed, integrative physician or functional medical provider before beginning any supplements or medications. By signing up for the patreon,you acknowledge that your health is your responsibility only.

There aren’t too many things that scare me. I’m usually pretty optimistic about the future, and I generally tend to think that are a lot of ways to ‘correct’ the mistakes we’ve made as a society regarding our health

But I’ll be honest…this scares me. Not for myself or my family. For everyone. I don’t say this with the intention to scare or fear monger you. I just want this to be a loud wake up call so you can take necessary action

What follows in this article is an exceptionally concerning subject regarding the health of both my country and the world. I hope you take this very seriously, especially if you or a family member was vaccinated

First, some history

Simian virus 40 (aka SV40 as it’s commonly reffered to) is a small DNA tumor virus originally discovered in monkeys. This polyomavirus gained a ton of notoriety in the mid-20th century when it was identified as a contaminant in polio vaccines that were developed using monkey kidney cells.

Yes, this really happened. It’s not a conspiracy. There’s decades of research on it now

The implications of SV40 for human health have been the subject of extensive research and debate, particularly concerning its potential role in cancer development.

In the early 1960s, the widespread use of polio vaccines, notably the inactivated poliovirus vaccine developed by Jonas Salk, inadvertently introduced SV40 into human populations

The vaccines were produced using rhesus monkey kidney cells that were naturally infected with SV40.

Not a problem in monkeys. But it’s a different story in humans.

While the primary aim was to eradicate polio, the introduction of SV40 into the human genome raised concerns about its oncogenic potential—its ability to cause tumors.

The molecular biology of SV40

Research has demonstrated that SV40 can integrate into the host genome, leading to cellular transformations that may result in tumorigenesis (cancer). The mechanisms by which SV40 promotes cancer are complex and involve the disruption of cellular regulatory pathways. Specifically, SV40's large T antigen has been shown to interfere with tumor suppressor proteins such as p53 and retinoblastoma protein, promoting uncontrolled cell proliferation.

Epidemiological evidence

Recent studies have provided compelling evidence that SV40 is not merely a relic of past vaccine contamination but is actively spreading within human populations. This means if your grandparents got it, your parents and you likely have it in your genome as well. Immunological assays and molecular biology techniques have detected SV40 DNA sequences in various human cancers, including brain tumors, bone sarcomas, malignant pleural mesotheliomas, and lymphoproliferative disorders. These findings indicate a higher prevalence of SV40 in cancerous tissues compared to normal tissues, suggesting a potential association between SV40 infection and the development of certain malignancies (cancer)

It’s believed that the introduction of SV40 into the genome is what initiated Nixon ‘war on cancer’, as rates dramatically exploded thereafter

Here’s where it gets even worse …

Recent, unpublished data out of Germany (dryman et al), as well findings from the lab of Philip Buckhaults (a cancer genomics expert) reports that the COVID vaccine is ‘contaminated with plasmid DNA’, with similar risks to SV40. The papers out of Germany claim the vaccines contain ‘60 billion copies of SV40-like promoter in each dose of the Moderna and Pfizer vaccine’

In other words, your risk of developing cancer at some point in your life, specifically if you received the Moderna or Pfizer vaccine that used the mRNA platform, is likely significant. Or at least much higher than the average population.

You can listen to Philips senate hearing on the issue here bellow. I would also suggest listening to Kevin McKernan’s hearing bellow as well so you understand the gravity of this issue you’re up against.

https://youtu.be/C7Qs166xR28?si=IDVRKF-YeBIi1s-A

https://youtu.be/G917QmY2mBI?si=Kg4ycXeIOpKXWJPs

The presence of SV40 DNA in specific cancer specimens has prompted a lot of investigation into its role as a potential co-factor in cancer development as well . For instance, studies have found SV40 sequences in pleural mesotheliomas, which are strongly linked to asbestos exposure. The interaction between SV40 and other carcinogenic factors raises important questions about the etiology of these cancers.

This is important to understand. It means that while SV40 alone may not be the sole cause these malignancies, its presence could exacerbate the effects of other carcinogens, leading to a higher risk of cancer.

That should be good news to you. It means that even if you did get the jab, there may be a lot of lifestyle decisions you can control to greatly prevent your risk of cancer, which is already extremely high (50% now) in the general population.

Understanding your new risk

‘intercalation’ into DNA refers to the ability of RAV40 to integrate into the host cell's genome. This process involves the virus inserting its own DNA into the DNA of the host cell. Unfortunately, if you got the mRNA vaccine, It’s possible this is likely an on going issue you will have to manage for the rest of your life.

The SV40 promoter likely impacts T cell motility by interfering with their signaling pathways, reducing their ability to move and respond effectively. This impairment can lead to "turbo cancer," where rapid tumor growth occurs due to weakened immune surveillance.

What can we do?

If you got jabbed, there’s a list of things that I think could be beneficial for you. we won’t cover all of the relevant lifestyle factors you should already be engaging in to stay healthy (like gut health, foundational nutrients, sun exposure, sleep etc). I think these should be obvious now, instead, we’ll draw attention to a few targeted therapies that I think all jabbed individuals likely need to consider

Thymalin

Peptides like thymalin may play a big role in enhancing immune function and potentially counteracting the effects of SV40 on T cell motility and overall immune response. I’ve already had create success using thymalin for long COVID in particular.

Thymalin is a peptide derived from the thymus gland. It stimulates T cell production and enhance their function. By promoting T cell maturation and homeostasis, I think thymalin could help restore T cell motility and activity that could be compromised by SV40. A lot of the blood work I’ve seen on jabbed patients usually indicates low T cell counts Thymalin also specifically boosts the proliferation and activation of T cells, improving their ability to migrate to tumor sites. In addition, thymalin is well researched anti-aging polypeptide drug for the thymus gland.

Dosing & souring — 10mg for 10 days, twice a year to maintain immune surveillance and health. Thymalin is a SubQ injection. It can be found on cosmic nootropics.

Cardiogen

Cardiogen is peptide that I believe could be particularly useful for vaccinated individuals. Cardiogen is a short chain peptide bio-regulator. You may have seen it mentioned specifically in Ryan’s heart failure protocol. Cardiogen is the primary bio-regulator for the heart, but it’s also been demonstrated to be experimentally useful against sarcoma (soft tissue cancers). This is particularly relevant and worth considering, as many of the alleged ‘turbo cance’ risks from vaccination ARE from soft tissue cancers in particular.

Cardiogen also appears to up regulate p53 expression and therefore apoptosis (death) in cancer cells. If you recall above, SV40's T antigen interferes with tumor suppressor proteins such as p53. This may be way to counteract that. While Cardiogen doesn’t have the experimental and clinical backing that peptides like thymalin do (if you had to choose one, that’s the peptide I’d go with), it has been well studied in other contexts (with the heart) and it’s entirely safe.

Deterium depleted water

While DD is not cheap, I think it’s one of the most powerful tools in the vaccinated individuals arsenal for cancer prevention, along with bi-anual courses of thymalin.

The presence of deuterium in water (heavy water) can impact cellular bioenergetics. By depleting deuterium, it is believed that the mitochondria can produce energy more efficiently, which may help normal cells thrive while we hinder cancer cell metabolism. Deuterium also directly influence various cellular signaling pathways. Lowering deuterium levels has been well-demonstrated in trials to disrupt the signaling that encourages cancer cell growth and division.

DD will probably run you somewhere around $200-300 a month depending on how much water you drink. It’s not for everyone, but it is an option worth considering if you’re particularly high-risk or simply wish to take advantage of as many preventative strategies as possible. It can also be used to treat cancer, but I would always suggest working with an informed physian or reaching out to the Center for Deuterium for guidance.

Litewater is my preferred source. Diluting 1/4 of daily drinking water with 10ppm DDW is standard practice.

Repurposed anti-parasitic drugs

Ivermectin and fenbendazole are two anti-parasitic medications that have been recently been repurposed for treating long COVID, as well as cancer. I wrote about ivermectin specifically in the Clot shot protocol (which you can find here on patreon) for spike protein detox. They are easy to aquire and have minimal side effects when used appropriately. Many turbo cancer protocols that are being developed have ivermectin and fenbendazole at their core.

While we don’t have hard data on this yet, it’s possible that those who received the M or P vaccine may need to use drugs like ivermectin and fenbendazole for the rest of their life (in cycles) as a cancer prevention strategy. At the very least, I would suggest looking into the clot shot protocol recommendations for ivermectin, and consider these on an anual basis under the guidance of an informed, intergrative physian.

For this reason, I also think the basic spike protein detox would be good for most jabbed patients to do at least 4-6 months out of the year minimum. I think at the very least, (if you just wanted to focus on one thing) I believe dissolve-it-all would be a good idea for ongoing spike protein clearance and clot prevention. This isn’t medical advice. It’s just my personal opinion.

Molecular hydrogen

Molecular hydrogen is one of my favorite cancer prevention strategies. While the machines used for hydrogen (particularly hydrogen inhilation discussed bellow) are a bit of an investment, molecular hydrogen is a versatile health promoting therapy that has numerous applications. I think everyone should own a device personally

(If you want to learn more about hydrogen, you can watch my interview with Dr Tyler LeBaron bellow — the worlds foremost expert on molecular hydrogen)

https://youtu.be/FZ86gJt12KA?si=0UfX59tvwBM0jqbR

Some studies suggest that hydrogen can influence the expression of genes involved in antioxidant defense, apoptosis, and cell cycle regulation, potentially creating an environment less conducive to cancer development. Because hydrogen is an extremely small molecule, it can diffuse directly accross the cell membrane and into the nucleus where it’s able to directly regulate gene expression, particularly p53. I think this could be extremely important for the vaccinated.

Hydrogen also selectively upregulates apoptosis, and there’s good research suggesting it may help target cancer stem cells, which are thought to play a key role in tumor initiation, metastasis, and relapse. This means it’s a phenomenal, versatile tool for prevention, treatment AND mitigating the risk of cancer reoccurrence.

I think hydrogen inhilation is best. This can be done for 30min all the way up to 3-4 hours daily (I think it’s good to take an occasionally week or couple days off if using it regularly).

Here’s the link to the device I use. Hydrogen water bottles (ONLY from this website) are also useful but I believe inhilation is superior.

https://hydrogen4health.com/product/hx900-pure-hydrogen-inhaler-with-pulse-mode-and-bg/

GHK (the ‘DNA resetor’)

GHK is another short, bio-regulator-like peptides that [quote] ‘upregulates a number of cancer suppressors and downregulates a number of genes associated with cancer progression’.

In another paper titled ‘GHK and DNA: Resetting the Human Genome to Health’ It’s mentioned that [quote] ‘GHK has been found to reset genes of diseased cells from patients with cancer or COPD to a more healthy state. Cancer cells reset their programmed cell death system while COPD patients cells shut down tissue destructive genes and stimulate repair and remodeling activities’

From this, we can almost think of GHK (like many of the bio-regulators) as intelligent-like, homeostatic regulator of the nuclear genome (how the genes are expressed) and a variety of cell signaling pathways. We don’t want something that’s going to push the body aggressively towards or away from apoptosis/programmed cell dealth on a system wide scale: we want things that REGULATE these functions specifically in the tissues and organs that need them.

This is important when discussing dissipative structures. This is what bio-regulators and hydrogen do. It’s why I hold them in high regard.

GHK is typically done in 10-20 day cycles, 2-3x a year, at 5-7mg daily (total daily dose), divided into two subq injections. One in the morning, and one in the evening. You can find it and all of the other peptides mentioned (aside from thymalin) on CanLabs. Some other peptide bio-regulators that may be worth throwing into your cycle are Vilon, Livagen and Epitalon.

Other peptides

Some other peptide bio-regulators that may be worth throwing into your cycle are Vilon, pinealon, cartalax Livagen and Epitalon. All of this peptides have also demonstrated anti-tumor properties by Inducing programmed cell death (apoptosis) in damaged or cancerous cells. Vilon in particular is a small fragmented thymic peptide with lots of anti-tumor properties. Epitalon and pinealon are also popular for their anti-cancer effects, meditated primarily through the regulation of melatonin and the sleep-wake cycle. This is another reason why blocking blue light, getting sun and going to bed on time is extremely important for cancer prevention. Cartalax regulates the extra-cellular matrix, and prevents cancer cell invasion and metastasis into tissues. It also regulates p53 expression.

These can all be found on CanLabs and the dosing for all the bio-regulators mentioned (exept for thymalin) is 1mg for 20 days, 2-3x a year based on what you can afford to run. Pinealon can be found on Amazon and other places in a capsule form as well.

Vitamin D

Numerous epidemiological studies suggest an association between higher vitamin D levels and a lower risk of various cancers, including breast, prostate, and colorectal cancers. This is particularly why sun exposure has strong associations with reduced all-cause mortality and a variety of cancer types, including even melanoma. I would suggest getting your vitamin D levels checked. If you can get your vitamin D levels up from direct sun exposure (30-60min 4-5x a week is ideal, and it needs to be mid-day) this is best. If you’re still low, you may want to consider a supplement 4-5 months out of the year, particularly in the winter. I’m also a big fan of the Sperti Vitamin D lamp for those that live at high altitudes. 3-4min, 4-5x a week is all that’s required.

For supplements, I like a single dose of the brand D.velop in the morning or mid-day with a fat containing meal

Sun bathing

Vitamin D can also increase the expression of chemokine receptors on T cells, which are essential for their movement toward sites of infection, inflammation and cancer. This allows T cells to migrate more effectively through tissues and toward areas where they are needed.

However, sun exposure (particularly UV light) also has many non-vitamin D dependent pathways for immunity. UV light directly influence various immune cells.

For example, UV exposure has a DIRECT affect dendritic cells in the skin, which play a key role in initiating immune responses. Dendritic cells capture antigens and present them to T cells, activating them. This interaction also promotes T-cell mobilization and enhances their motility around the body. A critical component of immune survilence that ‘catches’ cancer before it can spread.

Conversely, blocking artificial light at night is also the second half of this equation, as many of these processes are ACTIVATED by sun exposure during the day, but CARRIED OUT at night. Artificial light at night tells your body it’s still daytime, throwing off the periodicity of these delicatly timed regulatory mechanisms and immune mediated pathways. Sleep (in the absence of artificial light) is when cellular housekeeping takes place.

Key takeaways — block blue light at night. Use blue light blocking software (like Iris on laptop), color filters on phone, and blue light blocking glasses. Use very dim, red light bulbs in lamps instead of blue light emmiting bulbs. Bon charge sells good ones. Turn off overhead lights

Sulphurophane

Sulforaphane is an antioxidant found in cruciferous vegetables like broccoli. It’s even higher in broccoli sprouts and has a variety of anti-cancer properties.

For one, It activates the Nrf2 pathway, boosting antioxidant enzymes that reduce oxidative stress and protect DNA. Unlike traditional antioxidants, sulforaphane specifically activists the Nrf2 pathway so that the body can upregulate its own defenses in specific response to stress and environmental insults.

Another really important comment of sulph is that it Induces cell cycle arrest and promotes apoptosis (cell death) in cancer cells. It also enhances phase II detoxification enzymes, helping eliminate carcinogens and Influences DNA methylation and histone modification, affecting gene expression related to cancer.

It may also inhibit self-renewal of cancer stem cells, reducing tumor initiation and recurrence similar to hydrogen (hydrogen also impacts the NrF2 pathway)

I personally prefer to get it from broccoli sprouts, which have the highest concentration of any food. You may be able to find these at health food stores like Whole Foods. It can be taken as a supplement as well. If you can find sprouts, I think that would be best. If you want to supplement with it, I’d recommend no more than 10mg, 3-4x a week. You can also grow your own sprouts.

Modified citrus pectin

MCP is probably one of the most well studied supplements of nutraceuticals for cancer prevention and treatment. It has great synergy with conventional cancer treatments (which is rare for many supplements) and has a wide variety of mechanisms through which it works to prevent cancer metasis.

MCP can interfere with the ability of cancer cells to metastasize (spread to other parts of the body). It does this by blocking galectin-3, which is a protein that helps cancer cells adhere to each other and to blood vessels. MCP has also been shown to enhance the immune response (without exacerbating auto immune conditions) by activating immune cells in a balanced fashion, helping the body to better identify and eliminate cancer cells. MCP is a great alternative to thynalin for those that don’t want to do injections.

MCP has been shown to bind to heavy metals and toxins like glyphosate, potentially reducing the toxic load on the body. As mentioned, things like SV40 are a much larger problem when the body is exposed to carcinogens. Pectin combined with sulphurophane (which has also been shown to help excrete inhaled carcinogens from smog) is a powerful cancer prevent strategy.

Pectasol (and products that use this patent form of citrus pectin) is the ONLY form of pectin you should use, as it’s the primary form that’s been used in clinical trials. Other forms have not been shown to be effective. I think 1-2 tsp ( many like to statt slow with half a tsp for a few weeks since it can cause diarrhea in some) daily (needs to be ok an empty stomach away from other supplements. Great to take in the morning before food), for 1-2 months, followed by a 1-2 month break and then repeated through the year , could be a useful cancer prevention strategy.

How to reconstitute and use peptides (for eductional material only)

https://youtu.be/CXddqy62IWw?si=wnoWnPFEPLfIgIah

Peptide sources

https://canlabintl.com

I will continue to update this article if I find more things that are useful