Kelleigh Nelson was on Rense last night and talked about this report and research. How this is very encouraging and needs to be known that it is so easy to get the fenbendazole or mebendazole and there is really no way you can OD on this protocol. It is called fenben for short. Protocol three days on and four days off for brain cancer. She also said that people have been taking fenben along with ivermectin to treat all different types of cancer. The patient in this report says he took one 1-gram packet of powder (contains 222 mg of fenbendazole) each day for three days, and then taking four days off and repeating the process. This requires one package a week. He plans to stay on it for the rest of his life. He is in total remission. They are concerned of price gouging with this medicine when the public learns of this information. More information at the bottom of this page with links you will want to investigate for yourself.
Cancer has become a $500 billion-a-year business. Cost figures continue to skyrocket with some novel cancer therapy agents costing over $60,000 a month and the average agent totaling around $10,000 a month. Add on hospital expenses, doctor fees, radiation, homecare, etc., and the average dollar amount can easily run into the hundreds of thousands.
There are approximately 1,500 cancer centers in the US alone. MD Anderson employs more than 20,000 people, including over 1,600 faculty members. They treat more than 100,000 patients each year.
Behind MD Anderson, there’s Memorial Sloan Kettering in New York City, Mayo Clinic in Rochester, Minnesota, Dana-Farber/Brigham and Women’s Cancer Center in Boston, UCLA Medical Center in Los Angeles... and the list goes on and on.
Cancer is just one example of how misguided our vision has become when it comes to the treatment of disease. We see a similar pattern with heart disease, diabetes, obesity, depression, arthritis, and practically every other ailment.
We no longer talk about cures. The focus has shifted to developing drugs and programs that manage and control disease. There’s no money in curing and eliminating diseases. But there’s a never-ending profit stream associated with managing them.
It’s hard to believe that the primary goal of these cancer facilities is to find a cure and put themselves out of business.
If a universal cure to cancer is discovered, rest assured the industry will make it difficult to obtain, and it will cost an absolute fortune. None of the mission statements of these centers, that I read, mentioned the goal of shutting down. Quite the contrary, the emphasis was on growth and expansion.
I could rant forever about this misguided path. But that’s not my focus. My focus, as always, is to help you have the tools and knowledge to protect yourself and the ones you love.
However, it helps to understand the background as to why safe and effective therapies, such as this dog dewormer, aren’t widely publicized.
All About Fenbendazole
The dewormer is called Panacur C. The active ingredient is fenbendazole (FenBen for short). Fenbendazole belongs to a family of drugs called benzimidazoles, which have been safely utilized as anthelmintics for roughly six decades. Anthelmintics are compounds used for the treatment of gastrointestinal parasites like giardia, roundworms, hookworms, whipworms, and pinworms.
Merck & Co. commenced the use of selective anthelmintics around 1961. They were initially given only to animals, but human use soon followed. Fenbendazole is the anthelmintic typically found in animal products. A sister product to fenbendazole, mebendazole, is typically found in deworming products for humans.
Fenbendazole is administered orally in both large and small animals including dogs, pigs, cats, cattle, horses, rabbits, and fish. When given as directed, it is considered extremely safe.
Although fenbendazole has traditionally been considered an animal anthelmintic, when taken orally it has also been shown to be very well tolerated and safe in humans. While observations in humans are limited, based on the data, a single oral dose up to 2,000 mg per person, or 500 mg per person for 10 consecutive days, wasn’t problematic. There’s even one case where a 67-year-old patient with a very rare and severe parasitic infection of the liver took around 3,000 mg per day of mebendazole continuously for 13 years without toxicity issues (J Hepatol 1998 Dec;29(6):994–8).
In a clinical trial conducted at Johns Hopkins, no reports of toxicity or other problems were seen in patients taking 200 mg of fenbendazole per day. Over the years, there has been a lot of research that explains exactly how fenbendazole works at destroying parasitic worms as well as cancer cells. So far, there appears to be four different modes of action.
First, around the nucleus of all living cells, there exists a protein-structured microtubule network. These microtubules are involved in cell division, the cell being able to adapt its shape to a changing environment, and the movement of compounds within the cell.
Fenbendazole binds to tublin, a structural protein of these microtubules. This creates a blockage in the tiny tubes and prevents the removal of waste products and the intake of nutrients. The uptake of glucose, the sole energy source of the parasitic worms, is shut down. Without an energy supply, the worms are either paralyzed and die, or they are expelled from the body.
Cancer cells also require glucose as an energy source. By blocking the microtubular network of cancer cells, fenbendazole helps to shut down their energy supply and destroys them.
Second, fenbendazole further reduces the glucose uptake of cancer cells by downregulating what are called GLUT transporters. These are proteins that deliver glucose molecules one by one across cell membranes.
Third, fenbendazole increases the activity of the body’s natural killer cells in the presence of P53 tumor suppressor genes.
Fourth, fenbendazole acts as a kinase inhibitor, which helps block the formation of new blood vessels necessary for tumors to survive.
These anticancer properties are not new. They were documented years ago. I was able to find one of the earliest studies, published in 2002, which detailed these effects (Clin Cancer Res 2002 Sep;8(9):2963–9).
In 2002, while working at MD Anderson, Dr. Tapas Mukhopadhyay and his colleagues reported that mebendazole elicited a potent antitumor effect on human cancer cell lines both in vitro and in vivo. In simple terms, mebendazole (for all practical purposes the same drug as fenbendazole) strongly and profoundly inhibited the growth of lung, breast, ovary, colon, and bone cancer cells in both tissue samples and in live animals. At the same time, it had no negative effect on normal cell growth.
This same study was supported by a grant from the National Cancer Institute. It makes you wonder why they would fund a study like this, get such amazing results, and then not have enough interest to do a follow-up study or further pursue a drug with such potential.
Later in 2012, Dr. Mukhopadhyay and colleagues, at Panjab University in India, published another study showing that fenbendazole was a potent compound for inhibiting the growth of cancer cells without doing any harm to or affecting the growth of normal cells.
And in 2018, Dr. Mukhopadhyay and colleagues published yet another study highlighting fenbendazole as a safe and inexpensive anthelmintic drug possessing “efficient anti-proliferative activity” in human cancer cells. (This basically means it inhibits the growth of cancer cells.)
https://www.amazon.com/gp/product/B0CHPTN3Q1/ref=ox_sc_act_title_1?smid=A2VRIPQINS13AX&psc=1 or this link
https://www.amazon.com/gp/product/B0C94R1VH8/ref=ox_sc_act_title_1?smid=A39LHVHBGNZSZZ&psc=1
or if you could find out how to measure out panacur with 222 mg. It would be a lot cheaper I suppose. Maybe you can figure that out. Those on amazon are a little pricey. But the product you get lasts a lot longer, with 180 pills which would last a long time. So you have to do the math.
Actually this one has third-party testing and is probably the best quality. https://www.amazon.com/gp/product/B0CMHQG135/ref=ox_sc_act_title_1?smid=A1RQG8GGTD0CZ&psc=1
https://healnavigator.com/treatments/fenbendazole-cancer-protocol/
In that same report, Dr. Mukhopadhyay states, “FDA as well as other published pre-clinical data on the toxicological studies performed on animals shows that fenbendazole administered in different species at dosages several times the a with approved dosage does not cause any adverse effects in animals. Further, our previous study also showed minimal toxicity of fenbendazole in normal human cells. Considering this information, [fenbendazole] can be an ideal candidate for development as an anti-cancer agent” (Scientific Reports 2018 Aug 8(1):11926).
MD Anderson isn’t the only facility that has knowledge of fenbendazole. I suspect practically every cancer center knows about it.
For more on this study https://www.faim.org/a-cure-for-cancer-hidden-in-plain-sight