Fenbendazole Cancer Protocol

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Fenbendazole Cancer Protocol

The Fenbendazole Cancer Protocol has been gaining rapid interest in the past year following some amazing recovery testimonials.

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Fenbendazole Protocol – A Simple Step by Step Guide

The fenbendazole protocol people follow is surprisingly simple and includes a few added supplements to the fenbendazole:

  1. Fenbendazole 
  2. Curcumin
  3. CBD Oil
  4. Vitamin E

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  1. 1. Fenbendazole: One Packet a Day

Panacure Fenbendazole as a Potential Anticancer Drug

Fenbendazole which has 222mg of Fenbendazole per gram: one packet of powder per day for seven days a week. It can be mixed with food such as yogurt or simply taken by itself.

 

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  1. 2. Curcumin: 600 mg a Day

curcumin tippens

600 mg per day of bioavailable curcumin, which is the active agent in the herb turmeric. Curcumin may help increase healthy p53 levels, and it has been shown to be a potentially effective cancer therapy supplement.

 

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  1. 3. CBD Oil: 25 mg a Day CBD Fenbendazol Protocol

25-milligrams daily, taken sublingually (under the tongue). The CBD oil should be high-purity level broad-spectrum. CBD has been shown to potentially modulate tumor growth.

 

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A nurse’s tip:

  • It is important to choose the right CBD for medical use: flower-derived, lab-tested, organic, whole-spectrum.
  • To enhance CBD healing response for cancer symptoms, slowly increase to .5ml of CBD twice daily for a total of 50 mgs. 

 

Some people using this protocol use CBD oil while others chose to add THC. If you are considering adding THC, it is advised to use a Medical Cannabis Professional.

 

  • Vitamin E Vitamin E fenben protocol

Vitamin E is an antioxidant that may benefit some people with cancer, as it has shown potential for helping to prevent, treat and control cancer.

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Fenbendazole for Humans Side Effects

Some research suggests that those who are weak from chemotherapy may experience more side effects than those not receiving conventional cancer treatment.

Some common side effects that have been reported include elevated liver enzymes, mild diarrhea, and mild stomach discomfort. 

If you are currently taking chemotherapy for your cancer, it is best to discuss with a medical professional if and how to add curcumin and vitamin E. 

 

 

Fenbendazole Cancer Protocol: The Scientific Data

As surprising as it sounds, there is documented research about de-worming medications and their effect on cancer. This dry and tasteless Fenbendazole powder has been shown to exhibit “significant inhibition of tumor growth” when supplemented with vitamins A, D, E, K, and B.

 

Fenbendazole is a triple-threat to cancer: it kills cancer cells in three ways which are significant:

  • It destroys microtubules that sustain the structure of the cancer cell and its ability to divide and multiply rapidly.
  • It interrupts the cancer cells’ ability to process sugar, and cancer cells must metabolize sugar to survive.
  • It boosts the production of a cancer-killing gene called p53, a gene cancer patients may lack. When p53 becomes mutated or can’t keep cancer cells in check, cancer cells can proliferate.

The de-wormer also works against parasites, which might be the origin of some cancers.

 

Other Research That Supports the Use of De-Wormers for Cancer

There’s another “sister” drug of Fenbendazole, called Mebendazole, a de-wormer medication prescribed to treat parasitic worm infections in humans. Mebendazole has shown promising results for treating cancer (Lung, Melanoma, Glioblastoma, Colon, and others). 

 

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Laurie was battling triple-negative breast cancer. She began chemotherapy and was adding high amounts of Fenbendazole daily. “I believe that the combination of Fenbendazole and chemo worked very well.”

Fenbendazole Cancer Protocol- Relevant Research and News

Repurposing Drugs in Oncology (ReDO)—mebendazole as an anti-cancer agent

Mebendazole, a well-known anti-helminthic drug in wide clinical use, has anti-cancer properties that have been elucidated in a broad range of pre-clinical studies across a number of different cancer types. Significantly, there are also two case reports of anti-cancer activity in humans. The data are summarised and discussed in relation to suggested mechanisms of action. Based on the evidence presented, it is proposed that mebendazole would synergise with a range of other drugs, including existing chemotherapeutics, and that further exploration of the potential of mebendazole as an anti-cancer therapeutic is warranted.

Mebendazole elicits a potent antitumor effect on human cancer cell lines both in vitro and in vivo

We have found that mebendazole (MZ), a derivative of benzimidazole, induces a dose- and time-dependent apoptotic response in human lung cancer cell lines. In this study, MZ arrested cells at the G(2)-M phase before the onset of apoptosis, as detected by using fluorescence-activated cell sorter analysis. MZ treatment also resulted in mitochondrial cytochrome c release, followed by apoptotic cell death. Additionally, MZ appeared to be a potent inhibitor of tumor cell growth with little toxicity to normal WI38 and human umbilical vein endothelial cells. When administered p.o. to nu/nu mice, MZ strongly inhibited the growth of human tumor xenografts and significantly reduced the number and size of tumors in an experimental model of lung metastasis. In assessing angiogenesis, we found significantly reduced vessel densities in MZ-treated mice compared with those in control mice. These results suggest that MZ is effective in the treatment of cancer and other angiogenesis-dependent diseases.

Fenbendazole Enhancing Anti-Tumor Effect: A Case Series

Background: Fenbendazole (FBZ) is a cheap and readily available anti-parasitic commonly used in veterinary medicine. FBZ belongs to the benzimidazole drug class which destabilize microtubules through a mechanism similar to the anti-oncogenic vinca alkaloids. Although there are no reported cases in the literature, there have been several anecdotal stories published on website blogs with individuals praising its ability to treat a wide variety of cancers.

Case Presentations: Herein we describe the cases of three patients with various genitourinary malignancies who demonstrated complete response after receiving FBZ therapy as a single or supplementary chemotherapeutic agent. In two patient scenarios, they had experienced progression of metastatic disease despite multiple lines of therapy prior to initiation of FBZ. No side effects from FBZ were reported.

Conclusion: FBZ appears to be a potentially safe and effective antineoplastic agent that can be repurposed for human use in treating genitourinary malignancies. Further research is necessary to define the role of FBZ as a chemotherapeutic option.

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