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We're creating cancer patients out of healthy people, treating cellular adaptations as if they were death sentences, and in the process, causing more harm than the "cancers" we claim to prevent. The very foundation of oncology—its definition of what cancer is and why it occurs—represents a catastrophic misunderstanding of cellular biology, evolutionary adaptation, and the quantum biophysics of life itself. This misunderstanding has created a medical-pharmaceutical killing machine that profits from fear, while suppressing the profound truth: cancer is not a genetic mistake, but an ancient survival program, not an enemy, but a messenger, not irreversible, but capable of spontaneous resolution when we address its true causes.

Cancer is a prime example of how heavy metal toxicity, free radical damage, pathogen infection, inflammation, mitochondrial dysfunction, immune system depression, mineral and vitamin deficiencies, genetic mutation, cell wall damage, and oxidative stress all come together into an end-stage life-threatening condition. The best way is to address all these problems simultaneously, by trapping cancer tumors/cells in a lethal fire of concentrated nutritional substances.

An oncogene is a gene that causes tumors in animals and uncontrolled growth in cells in culture and cannot in and of itself change cells from normal to cancerous. It is the cells' surroundings, known as its microenvironment, that contribute in some way to how cancer has occurred. Cancer involves an interaction between rogue cells and surrounding tissue. The interaction between cancer cells and their micro and macroenvironment create a context that promotes tumor growth and protects them from immune attack or, on the other hand, prevent tumors from making any kind of beachhead so they cannot take hold or spread themselves around.

Cancer cells routinely form in most people's bodies. The surrounding cells and the surrounding extracellular matrix interact to shape cancer cell behaviors such as polarity, migration, and proliferation. The microenvironment includes complex scaffolding on which cells grow and develop, called the extracellular matrix. The microenvironment is what actually surrounds a cell. The extracellular matrix (microenvironment) has been shown to regulate gene expression, so it has more to do with the state of cancer than the cancer cells themselves.

A new study out of South Korea is raising serious questions about the safety of COVID-19 vaccines and boosters. The research, covering more than 8 million people, found that both mRNA and non-mRNA vaccines were associated with higher rates of six major cancers — and a 27% increase in cancer risk overall. Researchers found consistent links between vaccination and increased incidence of breast, colorectal, gastric, lung, prostate, and thyroid cancers, regardless of vaccine type or age group. Both major COVID-19 vaccine platforms appear to be carcinogenic.

The researchers divided 8.4 million South Koreans into vaccinated and unvaccinated groups, then followed them for one year. Compared to the unvaccinated, vaccinated individuals had a:

27% higher overall cancer risk
20% higher risk of breast cancer
28% higher risk of colorectal cancer
34% higher risk of gastric cancer
53% higher risk of lung cancer
69% higher risk of prostate cancer
35% higher risk of thyroid cancer

The odds of these results being random were “1 in 1,000.” mRNA vaccines from Pfizer and Moderna were associated with a 20% higher overall cancer risk, while non-mRNA vaccines — such as AstraZeneca and Johnson & Johnson — showed a 47% increase. Those who received a mix of vaccine types saw a 34% higher overall risk. The elevated cancer risks were not confined to one vaccine platform.

No vaccine technology was free of cancer risk in this dataset. The study also found that booster doses amplified the effect — with pancreatic cancer risk increasing by 125% and gastric cancer by 23%. Similar patterns are being observed in the U.K. The cancer risk rising steadily over time. It could go on for decades. It’s truly alarming.

Every demographic studied showed some elevation in cancer risk. Younger vaccinated people were more likely to develop thyroid and breast cancers, while older adults — especially those over 75 — had higher prostate cancer rates. Women overall showed a greater rise in colorectal and thyroid cancers, while men were more prone to gastric and lung cancers.

A Japanese analysis of 18 million people found higher mortality within a year of vaccination. Research from the Czech Republic linked vaccination to lower conception rates among women. An Italian study of nearly 300,000 people showed a 23% higher cancer risk after one or two doses, and a further 9% increase after three or more doses.

Governments, regulators, clinicians, and researchers must confront a sobering reality — nearly 70% of the global population has been injected with a carcinogenic product. The evidence demands immediate market withdrawal of these products. It’s now completely indefensible to continue any booster or variant vaccine program.

INTRODUCTION: THE REALITY BEHIND CANCER AND THE MEDICAL CULT

Cancer is not a one-size-fits-all disease. Different individuals with the same type of cancer can have different causes and responses to treatments.
Standardized treatments, including conventional and holistic ones, often fail because they do not address individual causes.
The fear surrounding cancer diagnoses and the overwhelming influence of profit-driven pharmaceutical companies exacerbate patient helplessness.
Oncologists derive about 65% of their income from chemotherapy drugs, highlighting a system designed to manage cancer for profit rather than cure it.

THE COST AND PROFIT MOTIVE IN CANCER TREATMENT

Global spending on cancer medicines reached $223 billion in 2023, with projections to rise to $409 billion by 2028.
Cheaper, less toxic drugs like ivermectin and fenbendazole show promise but are suppressed due to lack of profitability for Big Pharma.
The medical education system is dominated by pharmaceutical interests, limiting awareness of alternative treatments.

THE ROLE OF STRESS, ENVIRONMENT, AND CHRONIC DISEASE

Stress, especially chronic stress, suppresses the immune system, making the body vulnerable to cancer and other diseases.
Studies show that 6 in 10 American adults suffer from at least one chronic disease, and 4 in 10 will have cancer at some point.
Cancer rates are rising, especially among younger adults, with unusual increases in blood, breast, melanoma, colon, rectal, thyroid, and testicular cancers.

IRON AND CANCER CONNECTION

Excess iron is a powerful promoter of cancer growth, invasion, and metastasis.
Iron acts as a carcinogen by catalyzing free radical formation, suppressing immune cells, and feeding cancer cells.
Diseases like hemochromatosis that increase iron levels correlate with higher cancer risks.
Elevated iron promotes tumor formation by damaging DNA and cellular metabolism.

TOXIC ACCUMULATION AND CECLLULAR DYSFUNCTION

The accumulation of synthetic toxic poisons (e.g., pesticides, herbicides, heavy metals, microplastics) overwhelms the body's detox systems.
This leads to aberrant protein synthesis, chromosomal damage, and ultimately cancer tumors, which may be the body’s way of walling off toxins.
The medical community often fails to address nutrition and detoxification, focusing instead on symptom suppression through drugs that damage organs like the liver.

THE ROLE OF PARASITES AND MICROBIOME IN CANCER

Parasites are a significant and often overlooked cause of many cancers.
Many lesions diagnosed as cancer have been found to be parasitic infections misdiagnosed as tumors.
Parasites promote chronic inflammation, which is a known driver of cancer development and progression.
Examples include parasitic worms causing cancers and infections like Trypanosoma cruzi influencing cancer risk.

DMSO AND ALTERNATIVE CANCER TREATMENTS

Dimethyl sulfoxide (DMSO) is a naturally occurring, safe, and effective substance with healing properties across various diseases, including cancer.
When combined with hematoxylin dye (forming D-hematoxylin), it selectively kills cancer cells while sparing healthy tissue with virtually no toxicity.
Despite its effectiveness, DMSO has been banned by the FDA, likely due to its threat to profitable cancer treatments.

THE IMPACT OF MEDICAL RADIATION AND CONVENTIONAL TREATMENTS

Ionizing radiation from medical imaging (e.g., X-rays, mammograms) is a proven cause of cancer and other diseases.
Radiation damages DNA directly and through free radicals, leading to mutations and genomic instability.
Medical radiation contributes significantly to cancer mortality and ischemic heart disease, with no safe dose level.
Chemotherapy and radiation treatments kill healthy cells, cause immense side effects, and reportedly kill about 50% of cancer patients.
Many doctors themselves would refuse such treatments if terminally ill.

CANCER AS A DISEASE OF METABOLIC DYSFUNCTION

Cancer is not solely a genetic disease but a result of damaged cellular metabolism.
Environmental toxins, metals, radiation, and chronic inflammation disrupt mitochondrial function.
Nitric oxide promotes tumor growth by inhibiting cytochrome C oxidase, shifting metabolism from respiration to glycolysis (Warburg effect).
Proper mitochondrial function and sunlight exposure regulate energy production and reduce cancer risk.

THE FAILURE OF EARLY DETECTION AND CONVENTIONAL WISDOM

Early detection of cancers like prostate cancer does not improve survival rates.
Mammography screening may increase mortality in some cases due to radiation and tissue damage.
The common narrative of an “angry cancer cell” is a myth that has led to harmful treatments.
Cancer cells are injured cells attempting to heal; treatments that cause further injury are counterproductive.

IMMUNE SYSTEM AND CANCER DYNAMICS

The immune system constantly surveils and destroys cancer cells.
Immunosuppression, whether from stress, vaccines (notably mRNA COVID vaccines), or toxins, allows cancer to progress rapidly.
The COVID spike protein reportedly binds to tumor suppressor P53, undermining cancer cell regulation and immune surveillance.
“Turbo cancers” that grow aggressively post-vaccination are linked to immune suppression caused by the vaccine.

THE CALL FOR NATURAL HOLISTIC APPROACHES

Detoxification is key: reducing exposure to toxins in the environment, food, and personal products.
Natural therapies include grounding, sunlight, urine therapy, breathing exercises, prayer, and improving sleep.
Raising vibrational frequencies and improving nutrition counteract toxins and support healing.

SUMMARY AND CONCLUSION

Despite decades and billions spent on cancer research, effective cures remain elusive.
The cancer industry profits from ongoing treatments rather than cures.
Cancer treatments like chemotherapy, radiation, and surgery often increase cancer spread and mortality.
A paradigm shift is needed—from viewing cancer as a genetic war to understanding it as a metabolic and environmental disease.
Empowering patients with knowledge, detoxification, nutrition, and alternative therapies offers hope for true healing.

The U.S. Preventive Services Task Force's recent reversal on mammography guidelines, now recommends that women begin screening at age 40 instead of 50—a rollback that ignores decades of evidence showing screening's harms often outweigh its benefits. This policy shift fails to warn women about radiation exposure risks and the cascade of over-diagnosis and overtreatment that follows. There is a cynical expansion of a screening program that transforms healthy women into cancer patients. The new guidelines ignore the uncomfortable truth that X-ray mammography itself is carcinogenic, with cumulative radiation exposure potentially causing the very cancers it purports to detect. They ignore evidence that for every life allegedly "saved" by mammography, up to ten women are over-diagnosed and overtreated, subjected to surgeries, radiation, and chemotherapy for conditions that would never have threatened their lives.

If every girl in this country took 200 micrograms of selenium daily, breast cancer rates would drop by 82% in one generation. The breast cancer awareness movement itself was hijacked from its inception—with Imperial Chemical Industries (ICI), the chemical manufacturing giant that later spun off its pharmaceutical division as Zeneca (now AstraZeneca), founding Breast Cancer Awareness Month, while manufacturing both mammary carcinogens and chemotherapy drugs. This created a perfect profit loop: produce the chemicals that cause cancer, promote screening to find more 'cancers,' then sell the treatments. Every October, this pink-washing campaign actively actively suppresses discussion of environmental carcinogens' role in the breast cancer epidemic, while promoting detection and treatment.

Chemotherapy not only fails to stop cancer—but can actively spread it. Big Pharma medicine is a failing conventional oncology paradigm and its reliance on chemotherapy, and its ongoing coverup of its true ineffectiveness and devastating effects. It’s no mystery why chemotherapy will worsen cancer outcomes—the agents used are among the most toxic substances ever introduced into the human body, involving drugs like doxorubicin, cyclophosphamide, and paclitaxel—well-known for their genotoxic and mutagenic effects.

97% of the time, chemotherapy doesn’t work. Chemotherapy is still widely used not because it works, but because it’s profitable. Cancer is a holistic condition, not a reductionistic one. Mainstream oncology fails to address the root causes of disease and ignores the body’s terrain. Public donations and awareness campaigns disproportionately fund drug and surgical research, excluding nutrition, naturopathy, homeopathy, and Traditional Chinese Medicine.

Unlike antibiotics or most prescription drugs, doctors receive direct compensation for administering chemo. For example, a doctor might buy a chemo drug for $5,000, charge the patient $12,000, insurance covers $9,000, and the doctor pockets the $4,000 difference. This is a clear conflict of interest and likens it to a business model that would be deemed criminal in any other industry:

Doxorubicin intercalates into DNA and generates free radicals that cause double-strand breaks.
Cyclophosphamide is a nitrogen mustard derivative and Group 1 human carcinogen, according to IARC.
Paclitaxel impairs microtubule disassembly, disrupting mitosis in all fast-dividing cells.

These agents have a wide range of toxic and potentially carcinogenic effects, including:

Promote epithelial-to-mesenchymal transition (EMT),
Enrich cancer stem cell (CSC) populations,
Impair immune function, and
Lead to increased tumor resistance and recurrence.

Chemotherapy indiscriminately targets rapidly dividing cells—which includes:

Cancer cells,
Immune cells,
Gastrointestinal lining,
Hair follicles,
And children’s developing cells, which helps explain higher pediatric cancer vulnerability.

But most critically, chemo spares slow-dividing cancer stem cells—those that:

Self-renew,
Evade immune detection,
Resist standard treatments,
And regenerate entire tumor

KEY TAKEAWAYS:

Cancer causes toxic accumulation, parasites, radiation, iron overload, and metabolic dysfunction conventional treatment often harmful, profit-driven, with poor survival outcomes alternative treatments DMSO + hematoxylin, detox protocols, sunlight, nutrition, immune support immune system role critical in controlling cancer; suppression leads to rapid progression Medical Imaging Risks Ionizing radiation from X-rays and mammograms is carcinogenic parasites and cancer frequently misdiagnosed as cancer; major overlooked cause lifestyle & environment toxins in environment and lifestyle choices significantly impact cancer risk and progression.