When a therapy becomes predictable, it should serve humanity. But in the hands of power, that same predictability becomes a tool of control—not cure.
1. Introduction: The Birth of a Global Threat and Hope
In a world dominated by trillion-dollar pharmaceutical empires, I—a single researcher with no institutional backing—have invented and clinically applied a therapy that shows potential to outperform chemotherapy, immunotherapy, and radiation in treating solid tumors. With an investment of less than $140,000 over twelve years, my therapy has already demonstrated visible success in over 20 human cancer cases and several animal cases.
But this is not just about a miracle therapy. It is about what comes next. Will this life-saving solution become a tool of hope accessible to the world, or a new weapon of geopolitical dominance?
2. My Philosophical Framework: Why I Think This Way
My entire system is based on one philosophical axiom:
A person cannot manipulate a system whose outcomes cannot be predicted.
This belief defines the design of my therapy. I reject empirical randomness and statistical gambling. Instead, I demand predictability, verifiability, and transparency in both the biological mechanism and the delivery method.
Every component of my therapy—drug preparation, injection protocol, dosing schedule, and imaging feedback—is structured to follow a deterministic chain of cause and effect. This is not “trial-and-error” medicine. This is a logic-driven system that minimizes uncertainty and maximizes reproducibility.
In later sections, I will show how external tools, including advanced AI reasoning models, have been used to validate this internal consistency. But let me be clear: these tools did not generate the system—they only confirmed it.
3. A Therapy That Reflects the Philosophy
What is Intra-Tumoral ClO₂ Therapy?
A minimally invasive procedure: injecting high-purity chlorine dioxide directly into solid tumors under ultrasound guidance. The mechanism is reactive oxygen species (ROS)-driven tumor necrosis, which targets the tumor locally, causing cell death without systemic toxicity.
It Fully Aligns With My Five-Factor Model:
Tumor Suppression: Measurable reduction in tumor size or complete disappearance.
Side Effects: Practically zero systemic toxicity; patients remain active and healthy.
Resistance: No drug resistance observed across repeated treatments.
Repeatability: Protocol can be performed multiple times without degradation of effect.
Convenience: Requires only basic imaging tools and outpatient visits.
This model is not a gimmick. It is a formalized framework to evaluate all cancer therapies and mine scores at the highest level across all five parameters.
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