Cancer Prevention

This year alone, nearly 600,000 Americans will lose their lives to cancer. Recent estimates tell us that 41 percent of all Americans will be diagnosed with cancer during their lifetimes and 21 percent of the population will lose their lives to this devastating disease.[1] A new report released by the World Health Organization’s (WHO) forecasts that by 2035, an incredible 24 million people will be diagnosed with cancer globally.[2] These numbers reflect the need for a complete overhaul of our approach to cancer.

Despite being overlooked for decades, volumes of scientific evidence prove that diet and nutrition play a leading role in cancer development. Only in recent years have mainstream physicians and health groups begun to recognize the importance of our lifestyle choices when it comes to preventing and reversing cancer. Even the WHO report recommends a diet rich in fruits, vegetables and whole grains as a powerful way to help stave off this disease. Here is my list of anti-cancer superfoods that you can begin incorporating into your diet today for greater health and vitality. I’ve included dozens of scientific citations demonstrating the benefits of each of these nutrient-rich foods. Please click here to finish this article.




Ten suppressed  natural cancer  treatments: ********************************

Great list:  ************************************

Cancer is a preventable disease:

Sweet potatoes & cancer:
Most anti-cancer fruits:
Most anti-cancer Nuts:
Most anti-cancer vegetables:
Herbs that  inhibit vascular endothelial growth factor
Natural health products that inhibit cyclo-oxygenase-2 activity
Natural health products with potential direct and indirect anti-angiogenic activity
Curcumin / Berberine / Resveratrol ********************************************

Parsley has the highest amount of APIGENIN in it!

Bladder Cancer & mustard seeds:

Glutamine:  THIS IS HUGE!

Anti-Cancer Strategies: Inhibit Glutamine | Eat and Beat Cancer



Jun 24, 2017 – But what about glutamine, an amino acid, a building block of protein? … you can, however, eat foods that keep cancer cells from using glutamine. … avoid a steady diet of pepperseeds due to your body’s need for glutamine.).
Cancer as a preventable disease:



How To Make GcMAF:




Inhibition of P13K/AKt/mTOR Signaling by NATURAL products:


FENBENDAZOLE has anti-cancer potential ************************

For info on MEBENDAZOLE (same family)watch min mark 45-51.
Please listen to Joe 17 min. mark to 22 mins.

TIP of the hat to Joe Tippens and his blog!! A MUST READ!!
What Joe used:
Fenbendazole: 1 gram of Punacur C  (222 mg) of Fenbendazole each day for 3 days. Then OFF for 4 days. Repeat this each week. He took the brand Panacur, but any brand should work. (to be taken with a healthy fat like olive oil/coconut oil/avacado or avacado oil/ healthy nuts like raw walnuts/pecans/ect. works best with or right after eating my comments)

Vitamin E: 400-800 mg 7 days a week. Make sure it has Tocotrienol and Tocopherol forms. He used A product called Gamma E by Life Extension or Perfect E).

Bio-Available Curcumin: (600mg per day, 2 pills per day 7 days a week). He used A product called Theracurmin HP by Integrative Therapeutics.

CBD oil: (1-2 droppers-full [equal to 25mg per day] under the tongue, 7 days a week)
with or without THC.

Dr. Mercola & Dr. Klinghardt on parasites 39 min. – 44 min.
During an 8-wk facility treatment for Aspiculuris tetraptera pinworms with fenbendazole diet at our institution, human lymphoma xenografts failed to grow in C.B-17/Icr-Prkdcscid/Crl (SCID) mice. This well-established xenograft model is used to study the role of mitochondrial genes in tumorigenesis and usually results in 80% to 100% successful tumor growth within 21 d. However, during the facility treatment with fenbendazole, no tumors grew in 40 mice during the 30 d after injection. The mice in this study had not been diagnosed with pinworms but were part of a facility treatment. Rodents in this area customarily were fed a commercial irradiated diet (Global 2918, Harlan Teklad, Madison, WI). However the equivalent treatment diet containing 150 ppm fenbendazole was available only in a sterilizable form (2018S, Harlan Teklad) supplemented with vitamins A, D, E, K, and B (Table 1) to compensate for loss during sterilization. Because the animal facility was not configured for dietary sterilization, the sterilizable diet was fed unautoclaved, with the result that mice received higher-than-normal concentrations of vitamins. Therefore the observed antitumor effect could have resulted from either the additional vitamins or the fenbendazole. Therefore a controlled study was conducted to test whether fenbendazole, supplemented vitamins, or both in combination affected the growth of this human lymphoma cell line in SCID mice. SOURCE:

Although the original clinical approval for fenbendazole was for intestinal parasites and not for cancer, the drug has already gone through human clinical trials and so all of the clinical trial work related to toxicity has already been done and fenbendazole has been deemed safe for human consumption for many years.

Chris Woollams, former Oxford University Biochemist and a fonder of CANCERactive said, “Fenbendazole is yet another example of a cheap, safe drug intended for a specific health condition, which can be repurposed to be used to treat cancer. There is no doubt it has strong properties but some cancer experts prefer to use Mebendazole, which they obviously feel has more. We do have an article on CANCERactive about many such repurposed drugs from Metformin to Mebendazole.”
It is a very effective treatment for ulcers of the esophagus, stomach, and gut. … Panacur is particularly effective against Giardia, chronic low-grade Candida (yeast) and many fungal infections, both localized (toenails and ears) and systemic (skin/gut “allergies” and other syndromes.)

Cancer as a Parasitic Disease

Studies of other effects Studies with fenbendazole showed that the substance can be considered practically non-irritating to the skin and eyes. Fenbendazole was not a skin sensitizer when tested in a 10% formulation in guinea pigs. Fenbendazole seems to be well-tolerated in humans after oral exposure (single oral dose up to 2,000 mg/per person; 500 mg/per person for 10 consecutive days); however, observations in humans are limited.

I personally think that berberine should be a part of any cancer TX:
Berberine shuts down 6 pathways by itself & Feben 5 plus. 1. Fenben has very low toxicity to the body, meaning it will not mutate your DNA. As we all know, cancer cells become cancer cells due to mutations in our DNA. Chemotherapy cannot target only cancer cells; therefore, chemotherapy ends up damaging both healthy and unhealthy cells. When healthy cells are damaged, it causes mutations. Too many mutations will eventually lead to a cell becoming cancerous, aka new cancer cells. Fenben does NOT damage healthy DNA, so you are OK to take it, it will not hurt you. 2. Fenben is a VERY oily substance and MUST be taken with a fat to be absorbed into the body. Every drug has a specific bioavailability, which is defined as “the degree to which a substance is absorbed into the body”. Because Fenben is super oily it is not very soluble. The suggestion is to mix the Panacur with a tablespoon of olive oil and then chase it with whole milk to increase bioavailability. Be sure to mix and or chase with high-fat substances to ensure the drug absorption has enough bioavailability, so your body is taking up the full dose. You want to make sure you are giving the drug the best absorption! 3. Fenbendazole attacks tumor cells in 5 different ways, which is why it is so very powerful. First, it destabilizes the cell structure, basically collapsing the cell. Second, it blocks the glucose channels within the cell wall, which ends up starving the cell of the glucose it needs to survive. Third, because of the lack of glucose intake, the mitochondria inside the cell (which is the main energy source of all cells is also starved. Fourth, it turns on the P53 gene. The P53 gene is found in all cells. This gene is used to prevent cells from turning cancerous. When a cell mutates to the point of cancer, the P53 gene is turned off. Fenbendazole turns this gene back on, basically killing the cancer cell from the inside out. Fifth, it stops cancer cells from colonizing (forming a large mass). If cancer cells do not colonize, they do not create new solid tumor masses. —-
Increasing the bio-availability of  MBZ/FZ/ABZ:


First-pass metabolism of MBZ ensures that only about 20% of the oral dose reaches systemic circulation, with maximum plasma concentration, reached 2–4 hours post-administration. Dosing with a high-fat meal is known to modestly increase bioavailability []. Chronic dosing of MBZ increases plasma concentration by a factor of between two and three compared to single-dose []. In one series of patients treated with chronic MBZ at a dose of 40 mg/kg/day for hydatid disease, the mean peak plasma level was 137.4 ng/ml [0.47 μM] after a single dose of 10 mg /kg; however, there was high inter-patient variability (99.4–500 ng/ml [0.34–1.69 μM]). For patients not on chronic treatment, initial treatment of MBZ at the same dose produced a mean peak plasma level of 69.5 ng/ml [0.24 μM], (17.5–116.2 ng/ml [0.06–0.39 μM]) [].   SOURCE:

Another repurposed drug to look at Niclosamide:

For those of you that just think that cut / poison & / burn are the ONLY way to treat cancer please consider these other alnternatives that don’ t cause more harm than good. And DON’T cause secondary cancers.

Berberine is usually best used by taking 500 mg.’s 2-3 times a day for
two weeks then at least a week off & repeat. For more on this great supplement
look here:
Image result for jane mclelland metro map
Consider buying Jane McLelland book with her map & great info!
FULL list of supplements & repurposed drugs for cancer:

Blocking Cancer With Combinations of Supplements and Off-Label Drugs

The Flavone Luteolin Suppresses SREBP-2 Expression and Post …

by TY Wong – ‎2015 – ‎Cited by 15 – ‎Related articles

Aug 24, 2015 – Sterol regulatory element-binding protein (SREBP) –2 is a key transcription factor in cholesterol metabolism, and HMGCR is a target gene of SREBP2. Attenuating SREBP2 activity could potentially minimize the expression of HMGCR. Luteolin is a flavone that is commonly detected in plant foods.

EGCG inhibits Glutaminolysis pathway:

Green Tea Polyphenols Modulate Insulin Secretion by Inhibiting …


by C Li – ‎2006 – ‎Cited by 139 – ‎Related articles

Apr 14, 2006 – The upper panels show the reversal of EGCG inhibition by leucine and …. would block BCH-SIS by inhibition of GDH-mediated glutaminolysis.

Quercitin inhibits GLUT-1 pathway:

Quercetin inhibits glucose transport by binding to an … – NCBI – NIH


by KE Hamilton – ‎2018 – ‎Cited by 6 – ‎Related articles

May 29, 2018 – Quercetin inhibits glucose transport by binding to an exofacial site on GLUT1. Hamilton KE(1), Rekman JF(1), Gunnink LK(1), Busscher BM(1), .

MSM for TNBC & others:

Methylsulfonylmethane suppresses breast cancer growth by down-regulating STAT3 and STAT5b pathways.



A Drug Made for Animals and Taken by Humans to Treat Cancer: Fenbendazole


Another anthelmintic drug get attention as a repurposed anti-cancer drug. And science knows it for more than a decade… It works different than Fenben, Meben, Alben and Flubendazole and Niclosamide. But it is interesting and exciting. Read yourself the story:…/chinese-scientists-find-cancer-hope-……/s13046-019-1251-7…/artic…/pii/S0006291X16317429…
Melatonin & Cancer:

Viagra & Cialas repurposed for cancer:

A broad range of data, pre-clinical and clinical, has been summarised and presented to make the case that the commercially available and widely used PDE5 inhibitors sildenafil, vardenafil, and tadalafil are very strong candidates for repurposing as anticancer agents. These low-cost, low-toxicity drugs show potential to be included with current and emerging standard of care treatments in oncology. The combination with immune checkpoint inhibitors or possible use as perioperative therapies is particularly compelling strategies with the potential to positively improve survival outcomes in a relatively short time-frame.
Herbs for Autophagy:
Chloroquine for Sarcomas:


How Melatonin helps you live longer with cancer!

Flax seeds & or Budwig protocol:


Gum turpentine & Parasite cleanse: ZZZZZZZZZZZZZZZZZZZZZZZZZZZZ
Hulda Clark PDF For advanced cancers:,%20Hulda%20-%20The%20Cure%20for%20All%20Cancers.pdf

Cancer is parasites!

Cancer as a Parasitic Disease

Dr. Jennifer Daniels Turpentine | Cures Parasites and Candida



Jun 16, 2018 – Dr. Jennifer Daniels turpentine story began as a young girl raised in a poor … The 1899 Merck Manual lists 100% pure gum spirits turpentine as …


Ozone therapy:
Aiming for middle ground with iron:

Essiac tea:

Doctor V. does an excellent job with this video, especially #4

If I had cancer I would start by doing 2-3 day water fast. And intermittent after that!

Next step would be to kill the microbes in the cancer cells by using raw
organic honey as a trojan horse to get curcumin/ginger it into the cells.
And coffee enemas as shown here:

for more how honey & ginger/turmeric/Ceylon cinnamon kills the microbes please read:








Check out min mark 26 for Harvard Medical Studies on cancer supplements:

Then I would add the Budwig protocol
And some from this list of cancer superfoods listed here:


Rainforest herbs:

Cannabis oil with PubMed studies:
For more info on treating cancer naturally visit this blog page:  ***
A great mantra:
I give love and I receive, I love and approve of myself.
I love God and God loves me.
I know God wants me healthy, and I will trust in Him.
I can see God’s love healing me.
I love and approve of myself unconditionally.
For whatever harm I may have caused others, may they forgive me.
For whatever harm I have caused myself, I forgive myself.
I totally love and forgive myself unconditionally.
I spoke it, I believe it, AND SO IT IS!!
(Jim Schoellen)
Psalm 91: 14-16 “Because she loves me,” says the LORD, “I will rescue her; I will protect her, for she acknowledges my name. She will call upon me, and I will answer her; I will be with her in trouble, I will deliver her and honor her. W long life…   (Meditate on His word!)
Imagining that your cancer is leaving your body is good. Meditation is not.



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