Block Cancer’s Survival Pathways with Natural Cancer Treatment
Looking at my protocol compared to others—especially those who take just two or three supplements and sometimes enter remission—I recognize an uncomfortable truth. Even if you kill off every visible tumor on a scan, you may still have 100,000 to 10 million cancer cells hiding in your body. These rogue cells may circulate in the blood, linger in lymph nodes, or lay dormant in tissues. Unfortunately, a PET scan or MRI cannot detect cancer unless a tumor contains roughly 1 billion cells (10⁹). That’s why simply shrinking a tumor is not the same as curing cancer. To truly overcome it, you must shut down all 10 of the major cancer survival pathways and starve cancer cells of their fuel sources using a precise,
natural cancer treatment strategy.
The only way to do this is to strategically block every escape route cancer relies on. Cancer doesn’t just survive—it adapts. It reroutes around whatever you throw at it unless every pathway is addressed. These survival pathways include:
- Glucose metabolism (glycolysis): Cancer’s favorite fuel source. It ferments sugar into energy, even in the presence of oxygen.
- Glutamine metabolism: An amino acid cancer uses for growth and immune evasion.
- mTOR signaling: A protein-sensing pathway that tells cancer when to grow and divide.
- Autophagy recycling: Cancer hijacks this natural cleanup process to recycle defective proteins for fuel.
- Iron metabolism: Cancer uses excess iron to make DNA and generate free radicals for aggressive spread.
- Glutathione defense: A strong antioxidant shield that protects cancer from oxidative stress and immune detection.
- WNT/β-catenin signaling: Drives growth, stemness, and resistance to treatment.
- Microtubule stabilization: Helps cancer cells transport nutrients and resist chemotherapy.
- DNA repair mechanisms: Allows cancer to fix damage from chemo and radiation.
- Angiogenesis (VEGF pathway): Grows new blood vessels to feed tumors.
Blocking glutathione, the antioxidant shield cancer hides behind, is critical. I do this with berberine, green tea extract (EGCG), fasting for cancer, and low-carb OMAD (One Meal a Day). These tools suppress glutathione and leave the cancer vulnerable. Once this shield is down, the immune system’s NK cells and T cells can finally recognize and attack the enemy. Glucose restriction is a foundational step in any metabolic cancer therapy—cutting out sugar and starches begins the starvation process. But if you don’t also block backup pathways like mTOR, cancer will shift to using protein as fuel. This is often why late-stage patients begin wasting away when they stop eating—cancer switches to consuming defective cells and muscle tissue through autophagy.
If left unchecked, cancer will trigger cachexia, a deadly form of wasting, using the proteolysis-inducing factor (PIF) pathway to degrade muscle and consume organs. That’s why it’s not enough to just cut out sugar—you must block protein pathways, iron access, and recycling mechanisms. One of the lesser-discussed but powerful tools in this fight is the use of dewormers as supplements for cancer. Many patients have seen improvement using ivermectin, fenbendazole, and wormwood (Artemisinin), and there’s real science behind it.
- Ivermectin blocks the WNT/β-catenin pathway, disrupting cancer’s ability to self-renew and making it more vulnerable to chemo by disabling P-glycoprotein pumps.
- Fenbendazole disrupts microtubules, starving the cancer of glucose and halting nutrient transport.
- Wormwood (Artemisinin) reacts with iron to produce a burst of oxidative free radicals—a smart bomb inside cancer cells, especially in iron-rich tumors.
These compounds not only attack cancer directly, but may also help by reducing parasite-related inflammation, iron overload, and immune suppression. Still, dewormers alone are not a complete protocol. My approach uses them as part of a multi-phase natural cancer treatment—what I call Protocol 2.
In the Attack Phase, I fast and take oxidative agents like Artemisinin, high-dose ivermectin, berberine, Ursolic Acid, and even Capecitabine (a chemo pill). These increase ROS (reactive oxygen species) inside cancer cells, triggering oxidative stress, DNA damage, and apoptosis (cell death). But I also know these agents can cause collateral damage to healthy cells, especially if taken without breaks or recovery support. That’s why I include a daily Antioxidant Recovery Phase—a window after the kill phase where I take ALA, EGCG, quercetin, fisetin, resveratrol, and curcumin to help protect and rebuild my healthy cells while cancer is down.
Fasting for cancer and glutathione suppression keep the cancer’s defense low, and during this time, my immune system powers up. NK cells and T cells become more aggressive, more mobile, and more able to detect exposed cancer cells. All the while, Protocol 2 continues to shut down every cancer survival pathway, cut off the fuel supply, and support autophagy—but in my favor. By starving cancer, the body begins using it as fuel, recycling its defective proteins through clean autophagy. This triggers apoptosis, the natural self-destruct process of a cell.
With the right diet, OMAD, glucose restriction, glutathione suppression, and timed
oxidative and antioxidant phases, natural cancer treatment becomes complete.
Cancer isn’t just weakened—it’s left without fuel, defenses, or escape routes. That’s the core of my cancer remission strategy: shut down every survival pathway, activate the immune system, and let the body finish what it started.
