We found 84% of cancer patients treated with ivermectin + mebendazole saw their cancer COMPLETELY DISAPPEAR, SHRINK, or STOP SPREADING after 6 months.
The Chemotherapy Cartel is in FULL PANIC MODE.
🚨Anthropic just showed a 24-minute workshop on how to actually do prompts for Claude.
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🚨A Beginner’s Guide to Repurposed Antiparasitic Drugs in Cancer Research
@_Ivermectincure
🧬 1. Ivermectin
What it is: An antiparasitic drug approved for human use.
Cancer interest:
Shown in laboratory studies to disrupt cancer cell signaling pathways (e.g., WNT/β-catenin, mTOR).
May help inhibit tumor cell proliferation and induce apoptosis.
Anti-inflammatory and immune-modulating effects are also under investigation.
Research stage: Preclinical and very early-stage clinical research. There is currently insufficient human data.
Typical off-label use (anecdotal):
Doses vary; often 0.2–0.4 mg/kg, 1–2 times weekly.
Sometimes taken with fatty food to improve absorption.
Risks:
Possible liver stress and neurological symptoms at high doses.
Potential interactions with other medications.
🧬 2. Fenbendazole
What it is: A veterinary dewormer used for dogs and livestock.
Cancer interest:
Blocks microtubule formation in cells—similar to some chemotherapy drugs (e.g., vinblastine).
Some animal and cell studies suggest tumor suppression.
Popularized by Joe Tippens after claiming remission from lung cancer.
Research stage: Preclinical only—no formal human trials yet.
Typical off-label use (anecdotal “Joe Tippens Protocol”):
222 mg fenbendazole daily (often 3 days on, 4 days off).
Sometimes combined with: Vitamin E (gamma-tocopherol)
Bioavailable curcumin
CBD oil
Risks:
Not approved for human use.
Potential liver strain; product purity can be inconsistent.
No standardized clinical dosing or monitoring.
🧬 3. Mebendazole
What it is: A human-approved anti-worm drug (used for pinworms and whipworms).
Cancer interest:
Structurally similar to fenbendazole, but already approved for human use.
Inhibits microtubule formation in cancer cells, potentially halting cell division.
Has shown promise in preclinical and some early-phase human studies, especially for:Glioblastoma
Melanoma
Colon cancer
Research stage: Preclinical and early human studies (further along than fenbendazole).
Typical off-label use (under medical supervision):
100–200 mg/day, sometimes higher.
Often taken continuously or in cycles.
Risks:
Can elevate liver enzymes.
May cause gastrointestinal side effects.
Requires regular liver monitoring (AST/ALT).
⚠️ Note: These therapies remain experimental. Always consult a qualified medical professional before considering any off-label use.
Where can you buy ivermectin?
Visit: https://t.co/REwGZCdhg9
#CancerResearch #Ivermectin #Fenbendazole #Mebendazole
Roughnecks, the hard-working crew on oil and gas drilling sites, perform one of the riskiest jobs around a job that���s rarely mentioned but is essential to keeping our world running smoothly every day.
🚨Fenbendazole Research: From Deworming Drug to Potential Cancer Studies
@_Ivermectincure
Fenbendazole is a drug used primarily as an antiparasitic for animals. Its main use is to kill worms such as hookworms, roundworms, tapeworms, and whipworms.
This drug, known under brand names like Panacur and Safe-Guard, has been studied for potential effects in different types of cancer, including pancreatic cancer, prostate cancer, colorectal cancer, lung cancer, colon cancer, melanoma, lymphoma, and glioblastoma.
Fenbendazole has also been studied for activity against infections caused by Cryptococcus neoformans, an encapsulated fungus that can cause meningoencephalitis in immunocompromised hosts. Several studies have suggested that fenbendazole may also have anticancer properties. (Related: Moxibustion is an alternative therapy being studied for various health conditions.)
According to a 2018 article from Nature:
“Fenbendazole acts as a moderate microtubule destabilizing agent and causes cancer cell death by modulating multiple cellular pathways. The results, in conjunction with our earlier data, suggest that fenbendazole is a new microtubule-interfering agent that displays anti-neoplastic activity and may be evaluated as a potential therapeutic agent because of its effect on multiple cellular pathways leading to effective elimination of cancer cells.”
The authors of the article also cited potential anticancer mechanisms associated with fenbendazole, including disruption of microtubule function and proteasomal interference. Fenbendazole has also been studied as a possible adjunct to chemotherapy, radiotherapy, and metabolic therapies.
Although more commonly used in animals, fenbendazole is generally considered well-tolerated in humans at certain deworming doses, typically in the range of 5 mg/kg/day to 10 mg/kg/day under medical supervision.
Some discussions suggest it may have stronger effects when studied alongside other compounds such as ivermectin and various vitamins and supplements.
Fenbendazole has been proposed to affect cancer cells by interfering with glucose uptake and disrupting cellular energy processes, potentially limiting tumor growth.
When studied alongside vitamin supplementation, fenbendazole has been associated in experimental settings with antitumor effects. The vitamins used in such discussions include vitamins A, B, D, E, and K, which are known for their antioxidant and immune-supporting properties.
Vitamin E, for example, has been studied for potential anti-metastatic and antitumor effects in animal models. Similarly, adequate intake of B vitamins and dietary folate has been associated in some studies with reduced colorectal cancer risk.
Although fenbendazole alone does not have established clinical use in cancer treatment, it remains an area of interest in research exploring drug repurposing and combination approaches.
Fenbendazole has also been compared in mechanism to compounds like colchicine, which disrupt microtubule function.
Because cancer cells rely heavily on glucose for energy, researchers have explored whether fenbendazole affects glucose metabolism. In laboratory and animal studies, it has shown effects on cellular energy pathways and tumor growth dynamics.
While fenbendazole is primarily used in veterinary medicine, ongoing research continues to explore its broader biological activity. However, more clinical studies in humans are needed to confirm safety and effectiveness in cancer treatment.
Still early—human clinical studies are needed.
Visit👉@ivermectincure
#fenbendazole #ivermectinworks #cancerresearch
🚨 BREAKING NEWS: New Cancer Protocol Using Ivermectin, Ketogenic Diet, Fasting & Fenbendazole Published – Sept 2024
@_Ivermectincure
The 7-Therapeutic Hybrid Model for Cancer Treatment
1. Vitamin C
2. Vitamin D
3. Zinc
4. Ivermectin
5. Fenbendazole, Mebendazole & DON (Glutamine Antagonist)
6. Fasting, Ketogenic Diet & Ketone Metabolic Therapy
7. Press-Pulse Therapy, Endurance Exercise, Hyperbaric Oxygen Therapy, Methylene Blue, CoQ10, Niacin, Magnesium & Vitamin E
All dosages for these seven components are outlined in the protocol and are recommended to be followed for at least 12 weeks, regardless of cancer type.
Visit:- https://t.co/DNfK8i9GDG
Experimental at best, not standard care.
#Ivermectin #Fenbendazole #Cancer #CancerCure #Mebendazole
70% of the carrot sales in America are baby carrots
The majority of these baby carrots sold in America go through chlorine before being sold
Lab testing shows that chlorine is still present when being sold to eat
“Toxic chlorine byproducts like trihalomethanes are absorbed directly into the flesh — This is according to peer-reviewed research from Spain's University of Murcia.”
The levels are considered safe by the FDA.
🚨 THE 1939 CANCER ACT: THEY MADE CURING CANCER A CRIME! 🚨
In 1939 the British Parliament passed the Cancer Act.
It made it a literal criminal offense to advertise, offer, or even advise on ANY potential cure or treatment for cancer outside the official medical system.
Section 4 slams anyone who dares speak publicly about healing cancer.
Fines. Jail time. Career destruction. All for suggesting there might be another way.
And the United States quietly followed the same suppression model in that era.
Why would governments criminalize talk of cancer cures back in 1939?
Chemotherapy was in its infancy. Radiation was primitive. Survival rates were abysmal.
They weren't protecting people from "quacks."
They were protecting the future multi-trillion-dollar cancer industry before it was even born.
Natural protocols like Gerson therapy, Hoxsey herbs, laetrile, Essiac tea?
Systematically attacked, ridiculed, banned, or forced underground.
Decades later the "war on cancer" rakes in billions every year... yet overall survival for most major cancers has barely improved.
The 1939 Cancer Act is not patient protection.
It is profit protection.
It is cure suppression.
It is the smoking gun of the biggest medical cover-up in history.
Time to repeal it.
Time to expose it.
Time to demand real answers.
Who else is awake to this?
🚨 Protocol for Cancer – Ivermectin & Fenbendazole Dosing
@_Ivermectincure
Overview (for informational purposes only):
Several emerging research protocols are exploring the potential roles of antiparasitic agents—such as ivermectin and fenbendazole—in cancer-related metabolic pathways. These regimens are not approved cancer treatments and should only be considered within controlled research settings or under medical supervision.
Example Investigational Dosing Frameworks
Low Range:
Ivermectin ≤ 0.5 mg/kg | Fenbendazole 222 mg × 3 per week
Medium Range:
Ivermectin 1.0 mg/kg | Fenbendazole 222 mg daily (6 days/week)
High Range:
Ivermectin 2.0 mg/kg | Fenbendazole 444 mg daily (6 days/week)
Very High Range:
Ivermectin ≥ 2.5 mg/kg | Fenbendazole 888–1000 mg daily (6 days/week)
Visit :- https://t.co/da0kxPipn7
#CancerCures #Ivermectin #Fenbendazole #CancerResearch #Cancer
Our ENTIRE National Debt of $38 trillion truly IS due to elites stealing our taxpayer dollars?!
Catherine Austin Fitts, former Assistant Secretary of Housing and Urban Development, reveals how the US government stole $50 TRILLION taxpayer dollars and used Jeffrey Epstein to launder it.
Treasury Secretary Bob Rubin arranged Jeffrey Epstein's first visit to the Clinton White House in 1993, precisely as massive funds began disappearing from federal agencies, alleging Epstein ran the SWIFT system to launder the stolen TRILLIONS!
TRILLIONS vanished through undocumented adjustments at DoD and HUD starting in the mid-90s, escalating to $21 trillion by 2017 (matching the entire U.S. national debt then), plus $29 trillion in bailouts, totaling $50 trillion extracted while taxpayers are forced to hold the central banking debt trap in the form of our National Debt!
The Gates Foundation just upgraded their biological "vaccine" passport implants to install BOTH permanent quantum-dot QR codes and mRNA into your body
First developed in 2019, it’s been revamped with AI-readable tags that embed vaccination compliance data under your skin.
🚨 NEW: While every talking head screams "Iraq 2.0," @barbaramboyd explains what they'll NEVER tell you — 118 years of British financial control over Iran, and why Trump just struck the last piece on the Empire's chessboard.