Fenbendazole 222mg, Purity >99%, by Fenben Lab, Certified Third-Party Laboratory Tested, Analysis Report Included, 30 capsules

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While Fenbendazole for human cancer has gained more popularity in recent years, especially related to Joe Tippens’ cancer-fighting story, some research available at this time suggests Mebendazole might be more effective for treating some different types of tumors. For example, research studies have shown that MBZ could be more effective for brain and ovarian cancers. Fenbendazole has been found to be very effective against metastatic melanoma, lung cancers, and lymphoma. Anecdotally, both MBZ and FBZ have shown effectiveness against many cancer types, including when paired with vitamins, supplements, repurposed medications, alternative treatments, and standard of care treatments. If patients wish to take a higher dosage than 2000 mg of fenbendazole daily, it is best to consult a physician or oncology nurse. So with the Fenben, I looked into ways to render it more bio-available. I've also utilized DMSO in my past for various health protocols and am very familiar with it's pharmacology properties one of which is it's superior carrier abilities. When I catch a cold or virus, I put Oregano Oil on the bottoms of my feet which is often sufficient enough for the natural anti-biotic to get into my blood stream but I also put some DMSO on top of that and I can taste the oregano oil in my mouth within 30 seconds of applying it to the soles of my feet proving it's ability to rapidly carry medicine into the bloodstream. The limited studies suggest that Fenbendazole for humans is safe for consumption because it has low toxicity and a high safety margin. However, it is important to remember that the FDA has not approved Fenbendazole for use in humans.

Due to its antioxidant, anti-tumor, and anti-inflammatory activity, quercetin has been studied extensively. Quercetin can inhibit the spread of many cancers, such as prostate, cervical, lung, breast, and colon. Quercetin is not harmful to healthy cells yet powerful against cancer cells, making it a good candidate for a supplementary factor along with other anticancer medications. As much as five percent of people may have stomach-aches or loose bowels if they consume large amounts of fenbendazole without a break. Furthermore, restarting the protein p53 additionally prevents fuel genertion for cancer. When p53 is returned, it prevents the expression and actions of GLUT1 and GLUT4 transporters (glucose gates“) in the cells. ( Ref.) I feel strongly that it would be necessary to add another med to said regiment above. And that add will be: Nitazoxanide This may sound crazy but I called Moffitt and postponed the scans for 6 weeks. I felt that if I had the scans then, they'd likely reveal massive advancement. So I thought if the Fenben worked for me then who knows how long I'd have to wait for a followup MRI and I wanted to see results of the Fenben ... and again, I felt God's total guidance with this so I placed total faith in Jesus.Surprisingly, it seems that fenbendazole as well as other benzimidazoles exhibit a similar effect against tumor cells. Today it is thought that there are 3 main mechanisms in which fenbendazole kills cancer: In experiments examining the effects of hypoxia on cytotoxicity, cultures were grown in glass culture bottles and were made hypoxic by sealing the bottles with rubber gaskets, inserting needles for the influx and efflux of gases, and gassing with a humidified mixture of 95% nitrogen/5% CO 2, containing <1 ppm oxygen for 2 h before treatment. Fenbendazole (Sigma, St Louis, MO, USA) was then injected through the septum of the gasket, without breaking the hypoxia, and incubation under hypoxia was continued for 2 h ( 8, 9). In experiments examining the effects of fenbendazole on the radiation response of hypoxic cells, cultures were grown in permanox Petri dishes (MP Biomedicals, Solon, OH, USA), which allow for rapid outgassing of oxygen from the cultures ( 4, 8, 9). Immediately after addition of fenbendazole or vehicle, the cultures were placed in stainless steel pressure vessels and gassed with a humidified mixture of 95% nitrogen/5% CO 2, containing <1 ppm oxygen for 1 h at 37°C to produce severe hypoxia, then sealed, transported to the irradiator and irradiated. Aerobic cultures were treated analogously, but were incubated under 95% air/5% CO 2. Fenbendazole for cell culture studies was dissolved in dimethyl sulfoxide (DMSO; Sigma), diluted in Waymouth’s medium, and added to culture medium. Cell cultures were irradiated with 320 kV X-rays produced by an XRAD irradiator (Precision X-ray, Branford CT, USA) at 12.5 mA, 2 mm Al filtration, and a dose rate of 1.9 Gy/min (hypoxic cells) or 2.4 Gy/min (aerobic cells). Getting the proper fenbendazole dose for humans cancer is essential for patients who want to try the protocol. Dogra, N. (2018, August 9). Fenbendazole acts as a moderate microtubule destabilizing agent and causes cancer cell death by modulating multiple cellular pathways. Scientific Reports. https://www.nature.com/articles/s41598-018-30158-6 The key process of chemoresistance is whenever cancer cells adjust to being able to expel the medications from themselves through unique drug efflux pumps known as P-glycoproteins. Fenbendazole isn’t a target for p-glycoproteins, therefore it can’t be expelled from cancer cells when it gets in them.

Antitumor activity of albendazole against the human colorectal cancer cell line HT-29: in vitro and in a xenograft model of peritoneal carcinomatosis.CBD oil 25 milligrams. Consume one to two drops (total ~25 milligrams) under your tongue daily before bedtime. However, there is an increasing number of studies that confirm the fact that fenbendazole might truly increase the strongest tumor suppressor in our bodies – p53. ( Source)