Artemisinin is a natural compound extracted from the plant Sweet Wormwood (Artemisia annua). While it’s best known as a treatment for malaria, it also has powerful anti-cancer effects—especially when used at the right time and dose.
Artemisinin is unique because it creates free radicals (oxidative bursts) that are especially deadly to cancer cells—but only when iron is present. Since many cancers hoard iron, artemisinin becomes a guided missile in your protocol.
Why 1900 mg?
Cancer cells are tough, and lower doses of artemisinin may not produce enough of an oxidative effect. The 1900 mg dose is a therapeutic-level dose designed to:
- Ensure enough artemisinin reaches the bloodstream and tumor site
- Trigger a strong oxidative reaction inside iron-rich cancer cells
- Support radiation and fasting phases for maximum kill pressure
How Artemisinin Fights Cancer
Here are the three key ways artemisinin attacks cancer:
1. 🧲 Seeks Out Iron in Cancer Cells
Cancer cells often pull in 3–5x more iron than normal cells. This makes them an easy target for artemisinin, which reacts with iron inside the cell to create a burst of free radicals (ROS)—damaging the cell from within.
It’s like dropping a time bomb in the middle of the cancer’s engine room.
2. 💥 Triggers Oxidative Apoptosis
Once artemisinin reacts with iron, it creates oxidative stress, which:
- Breaks down cell membranes
- Damages mitochondria
- Triggers apoptosis (cancer cell death)
This works especially well when fasting or combined with radiation, because the cancer’s natural defenses are already weakened.
3. 🛡 Works Best When Antioxidants Are Low
Just like B17, artemisinin relies on oxidative pressure. If you take antioxidants like Vitamin C at the same time, they can block the free radicals and protect cancer cells.
That’s why artemisinin must be taken during fasted, antioxidant-free phases like the Metabolic Ignition Phase in the morning.
⏰ Why Take It at 6:30 AM?
The Metabolic Ignition window (6:30–6:50 AM) is when:
- The body is in deep fasting
- Insulin and glucose are at their lowest
- Antioxidants are NOT active
- Cancer cells are more exposed to oxidative damage
Taking artemisinin here:
- Ensures maximum oxidative damage to cancer
- Weakens the tumor before radiation therapy at 7:30 AM
- Creates a strong synergy with fasting, Fenbendazole, and B17
weet Wormwood (Artemisinin) – Protocol 2 Summary (Corrected)
✅ Best Timing:
- 6:30 AM during the Metabolic Ignition Phase (fasted, antioxidant-free)
- Do not take during or after the Antioxidant Wave (~12:30 PM onward)
- No second dose at 2:30 PM OMAD — this was removed from the protocol to avoid conflict with antioxidants
💊 Recommended Dose:
- 950 mg at 6:30 AM, fasted and antioxidant-free
- Former second dose removed to avoid interference
- Take with fats (e.g., MCT oil or black seed oil) for enhanced uptake
⏳ Active Duration in Body:
- Peak effect: 2–4 hours
- Activity declines by 6–8 hours post-dose unless re-amplified by fasting or radiation
- Not stored long-term; effects are transient
🔁 Redundancy With:
- B17 (Apricot Seeds) and radiation therapy (all increase oxidative pressure) — synergistic, not redundant
- Do not combine with Vitamin C, Methylene Blue, or other antioxidants during active window
📉 Pathways Inhibited or Affected:
Promotes immune clearance of apoptotic cells indirectly
🔒 Final Summary
Iron metabolism targeting – generates ROS in iron-rich cancer cells
Intrinsic apoptosis pathway – triggers cell death through mitochondrial oxidative stress
NF-κB suppression – reduces pro-survival and inflammatory signaling
Anti-angiogenesis – may restrict blood supply to tumors
Artemisinin from Sweet Wormwood is one of nature’s most powerful oxidative weapons. It targets iron-loaded cancer cells and turns that iron into a tool for destruction. By using 1900 mg daily, split into two doses, and placing the first dose in the Metabolic Ignition Phase, you take full advantage of artemisinin’s explosive potential—just when cancer is most vulnerable.
In Protocol 2, this makes it a core pillar of the early-morning oxidative attack, especially when paired with fasting, B17, Fenbendazole, and radiation.
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