Watch this video where a man used an anti-parasitic drug to cure his cancer when he was given three months to live.
Here is how the Veterinarian knew to tell Joe Tippens to take the anti-parasitic drug Febendazole:
“He told me a story of a scientist at Merck Animal Health (the veterinary side of Merck) that had performed cancer research on mice by injecting different types of cancers into different mice body parts.
And this scientist stumbled (trial and error) across a product in their canine product line that was batting 1.000 in killing these different cancers.
He told me that the scientist in question got diagnosed with 4th stage brain cancer and was told “no hope, 3 months to live”.
This person decided “what the heck” and started taking the canine medicine. Six weeks later, she was all clear.
I had just been told I’ve got no hope and 3 months to live, so it wasn’t a hard decision for me to take the leap.”
So when my PET scan in September also turned up “all clear” (meaning I had most likely been all clear for 6 months), I decided it was time to “come clean” with my trusted oncologist (who I like and trust very much by the way).
But before disclosing everything to him, I decided I need to do a little “set up” first.
After he very excitedly told me the continued good news of being “all clear” for a second consecutive quarter, I asked him a “very loaded” question.
I asked, “Doc, what is really going on here? Can you disclose to me how I am doing versus all of the other patients on the clinical trial with the exact same condition”?
His answer was what I already suspected. He said, “Joe we can’t explain it, but you are kind of a sole data outlier right now”.
Meaning with hundreds of like kind patients, I was the only one with a cure. I knew then my other alternative regimen was largely responsible, but I decided to come clean anyway.
I said, “Doc, I’m glad you told me that about my results within the trial, because I have something to share with you”.
I proceeded to tell him all about the canine dewormer as I watched his jaw drop
His next words I’ll never forget (and remember for context he and I had become good friends by this time).
He said, “you little shit, I knew there was something up with you…..and….I’ve had some weird days here at MD Anderson, but this one probably tops them all”
His next sentence almost floored me.
He said, “You know, we’ve known for decades that these antihelmintic class of drugs (meaning to destroy parasites in the intestines) could have possible efficacy against cancer, and in fact in the 80’s and 90’s there was a drug called Levamisole that was used on colon cancer and it is an antihelmintic drug”.
I said, “Doc, if you have known for decades why hasn’t more work been done on it?”
His answer was honest.
He said, “probably because of MONEY…all of these drugs are far off-patent and nobody is going to spend a gazillion dollars to repurpose them for cancer…..only to have generic competition the next day.”
I knew he was right.
Joe Tippens blog link is below
Ernest Best and many others have cured their cancer too after being told they would die soon.
You can order Ivermectin, Mebendazole, Febendazole and Nitazoxanide here
DR. LEE MERRITT: THE PARASITE CAUSING CANCER PARADIGM & THE USE OF ANTI-PARASITICS AS A CURE.
Click HERE for Dr. Merritt’s printable guide to the Parasite Protocol
VIDEO PROOF CANCER IS CAUSED BY PARASITES
Cancer is a Microparasitical Infection, and
We All Have It
In a recent autopsy study of Multiple Sclerosis (MS) patients who died from the disease, ten out of ten (100%!!!) actually had microparasites inside the central nervous system including nematode small worms in the brain.
Alan Macdonald: Multiple Sclerosis is a parasitosis
P2X4 receptor controls microglia activation and favors remyelination in autoimmune encephalitis
Duray Research Foundation – Multiple Sclerosis
One of our goals is to establish a firm scientific platform for some cases of Multiple Sclerosis as a brain/spinal cord chronic infection.
In 2016, using our highly specific Molecular Beacon DNA probes, we detected the specific DNA of Borrelia in the autopsy CSF of multiple sclerosis victims.
Currently, it is taught in medical schools that all cases of Multiple Sclerosis stem from a degenerative condition of unknown cause.
Borrelia spirochetes were cultured from the spinal fluid of ten of ten Multiple Sclerosis patients by Dr. Oystein Brorson, MD and Dr. Sverre-Henning Brorson, MD in 2001.
In addition, all were positive for Borrelia spirochetes by Electron Microscopy.
This discovery helped make sense of what I had found in my Multiple Sclerosis study. If the MS patients had Nematodes and Borrelia burgdorferi in the central nervous system, then the proper treatment wasn’t just antibiotics but would have to be high dose antiparasitic drugs followed by antibiotics, and this combination would have to continue until all parasites in all their growth stages including eggs, had been cleared from the brain.
Why had so many missed this discovery?
In today’s fast-paced medicine, anytime MS is considered the CSF specimens are placed directly in an automated analyzer that looks for MS markers, but not for parasites. On a slide without stain, the CSF looks normal. Then if the lab looks at the slide at 40x magnification or higher, they will miss the worms. It’s like looking at an elephant’s leg an inch away and trying to figure out what the whole animal looks like.
What this means to MS patients?
Clearly this suggests that despite any other treatment, the MS patient should first be placed on an antiparasite medicine for nematodes, followed by antibiotics for Borrelia. Treatment would have to be aggressive to get past the Blood-Brain-Barrier, and prolonged to eradicate the Borrelia.
Dr. Paul Duray MD Research Fellowship Endowment Inc
In Dr Paul Duray’s career, he single-handedly expanded the number of Borrelia illnesses to include:
Borrelia-related Parkinson’s disease;
Borrelia-related intrauterine infections with fetal deaths;
Borrelia muscle diseases, fasciitis and cystitis;
Fatal Adult Respiratory Distress Syndrome (ARDS) due to Borreliosis;
Borrelia-related necrotizing splenitis;
He also published many landmark manuscripts which redefined and enlarged the medical and scientifc understanding of spirochetal diseases.
Nematode infestations of the CNS require very careful treatment and monitoring by an experienced physician. Patients should not attempt to self-treat with antiparasitic drugs. Some anthelmintics can cause severe inflammatory reactions which might require concomitant steroid treatment in order to avoid fatal encephalitis.
Clearly, this suggests that despite any other treatment, the MS patient should first be placed on an antiparasite medicine for nematodes, followed by antibiotics for Borrelia. Treatment would have to be aggressive to get past the Blood-Brain-Barrier and prolonged to eradicate the Borrelia.
Lyme disease (Borrelia burgdorferi) treatment: 2 herbal compounds may beat antibiotics
Parasites as Cancer Triggers: Click HERE
These clinical pictures caused by trichomonads correspond to the findings of Dr. Alfons Weber, who, however, lists even more clinical pictures.
2.5 Reactions of the host organism to the Plasmodium infection in the blood ; 2.5.1 kinetic impairment of blood circulation; 2.5.2 physiological impairment of blood circulation
2.6 damage to blood and lymph vessel walls ; 2.6.1 in the capillaries; 2.6.2 in the great arteries; 2.6.3 in the lymph vessels
2.7 cancerous tumor formation and resorption ; organism-specific and plasmodia-related growth substances; 2.7.2 Mitotic disorders, pathological giant cells
2.8 Manifestations on the skin and in the skin’s appendages ; 2.8.1 hair loss, disturbed nail formation; increased sweat and sebum production, acne, rosacea; psoriasis, scleroderma; 2.8.4 Infection of the oral cavity and tongue
2.9 Manifestation in the bones, joints and ligaments ; path and type of destruction by Plasmodium; 2.9.1 Polyarthritis, Bechterew’s disease; 2.9.2 Osteoporosis, osteomalacia
2.10 Manifestations in the brain, spinal cord and nervous tissue ; 2.10.1 Multiple sclerosis, Parkinson’s disease; 2.10.2 Sciatic and trigeminal neuralgia; Psychoses: schizophrenia, etc
2.11 Manifestations in the digestive organs : 2.11.1 in the stomach: gastric ulcer; in the small intestine: enteritis, flattening of the mucosa; 2.11.3 in the large intestine: ulcerative colitis, Crohn’s disease; 2.11.4 appendicitis; 2.11.5 in the rectum: hemorrhoids
2.12 Manifestations in the respiratory organs : 2.12.1 Bronchial asthma; 2.12.2 Pulmonary emphysema, pulmonary atrophy
2.13 Manifestations in the urinary organs : 2.13.1 glomerulonephritis, tubular nephritis, nephrosclerosis; 2.13.2 albuminuria, globulinuria; Disturbances in the evacuation of urinary substances: uremia, uricemia; 2.13.4 Lithiasis in the urinary organs: urinary stones, etc.
2.14.Manifestations in the genitals : 2.14.1 female genitals; 2.14.2 Complications in pregnancy; 2.14.3 diaplacental infection; 2.14.4 germinative infection; 2.14.5 male sex organs
2.15 Manifestations in the pancreas (diabetes)
For over 100 years there has been the theory that parasites could cause cancer or even “are the cancer”.
On March 28, 1891 an article was published titled “IS CANCER A PARASITIC DISEASE?“
This theory was proposed by one of the world’s most famous physicians of all time, Nobel Prize winner Robert Koch (1843-1910).
As a microbiologist, the discoverer of anthrax and tuberculosis was perfectly clear in theory.
Dr. Wilhelm von Bremer, published the article “Krebs – eine Erregerkrankheit” [Cancer – a pathogenic disease] in the journal “Fortschritte der Medizin” back in 1932
In 1962, Dr. Alfons Weber stated that in every tumor tissue there are microparasites.
For the first time he was able to prove Robert Koch’s theory and published film recordings in which one can see the parasites in the tumor tissue.
(The National Library of Medicine has a copy of the monograph that you can go view as they will not lend it out. Click here for info).
Alfons Weber countered by showing images in which the microbes actually caused the cell to burst, but shortly afterward they took over a new cell – quite normal for parasitic life forms, but impossible for cell organelles.
He also demonstrated that the microparasites multiply within the cell, which organelles do not.
He also provided proof that it was a microparasite:
In an experiment, Weber burned human blood under a 160-degree flame. All human cells were completely destroyed.
Weber added a glucose solution to the dead organ material and a short time later the microparasites were moving on the glass plate.
This experiment silenced all critics, but Weber’s research was still not recognized and hushed up in the future.
What does today’s science say about the topic?
The knowledge that cancer is caused by parasites has flared up again, thanks to the Russian chemist, epidemiologist and microbiologist Tamara Lebedewa.
Because she lost her entire family to cancer and none of her family members were cured by conventional medicine, she researched the disease “cancer” for 13 years.
Since she found that there was no causal cancer therapy in conventional medicine and the theory about “degenerate human cells” was never proven, she started her research from scratch.
Obviously, in 100 years of cancer research, no progress has been made. Why do you think that is?
Lebedewa found out that so-called cancer cells are actually unicellular parasites, called Trichomonas.
The flagellates have exactly the properties of so-called “cancer cells” and will be identified as such by every oncologist.
Not everyone infected with trichomonads automatically gets cancer.
Lebedewa found out that certain triggers let the microparasites proliferate.
These include poisons, drugs and a suppressed (lowered) immune system.
According to the scientist, the body reacts to the malignant growth with encapsulation, which is called “tumor” in conventional medicine.
This protective measure prompts the body to stop the overgrowth.
Once the tumor is damaged and tissue leaves the tumor, it continues to spread, which is called “spread”. The body will try again to encapsulate the “spread cancer” in what is called “metastasis”.
Parasites and heart diseases
Dr. José Ignacio Santos Preciado (parasite researcher at the renowned University of Stanford / California and General Director at the Hospital de México) and his team found out back in 2012 that this is the main cause of all cardiovascular diseases (heart attack, heart failure/CHF, Cardiac arrhythmias, angina pectoris, etc.) is the infestation of the heart with parasites. According to Dr. Santos Preciado triggered by parasites.
Parasites and Cancer Books: http://www.gesundohnepillen.de/weber1.htm
**CDC Warning about Neglected Parasite Infections in the United States
A Cat Parasite May Be Controlling Our Minds!
Toxoplasma gondii: An Underestimated Threat?
Negative Effects of Latent Toxoplasmosis on Mental Health
Sero-molecular survey on Toxoplasma gondii infection among drug addicted and non-addicted individuals: a case–control study
The Roles of Mast Cells in Parasitic Protozoan Infections
Repurposing Drugs in Oncology (ReDO)—chloroquine and hydroxychloroquine as anti-cancer agents
Breast cancer is the most diagnosed cancer in women in the world. Mebendazole (MBZ) has been demonstrated to have preclinical efficacy across multiple cancers, including glioblastoma multiforme, medulloblastoma, colon, breast, pancreatic, and thyroid cancers.
Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update
Emerging Perspectives on the Antiparasitic Mebendazole as a Repurposed Drug for the Treatment of Brain Cancers
Ginger extract treatment reversed T. gondii-induced pathological changes in the brain, liver, and lungs. These findings indicate that ginger extract could be a potential alternative therapeutic for treating chronic toxoplasmosis.
Herb Pharm Certified Organic Ginger Liquid Extract for Digestive Support – 4 Ounce
About this item
- Expertly extracted for digestive system support
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Click HERE for more REFERENCE STUDIES on using Anti-parasitic drugs for cancer.
Using Ivermectin for cancer
Recently, ivermectin has been reported to inhibit the proliferation of several tumor cells by regulating multiple signaling pathways. This suggests that ivermectin may be an anti-cancer drug with great potential.
Here, we reviewed the related mechanisms by which ivermectin inhibited the development of different cancers and promoted programmed cell death and discussed the prospects for the clinical application of ivermectin as an anticancer drug for neoplasm therapy.
Antitumor effects of ivermectin at clinically feasible concentrations support its clinical development as a repositioned cancer drug
In Vitro Effects of Ivermectin and Sulphadiazine on Toxoplasma gondii
Did you know that ivermectin treats cancer?
At least nine different peer-reviewed studies demonstrate how safe and effective ivermectin wards off the Big C, threatening the multi-billion dollar cancer industry. There are two industries, in other words, that ivermectin threatens: the covid industry and the cancer industry.
1) In 2017, research published in the journal Biochemical and Biophysical Research Communications found that ivermectin preferentially treats renal cell carcinoma (RCC) while protecting normal kidney cells. RCC tumor growth is also delayed by ivermectin, which induces mitochondrial dysfunction and oxidative stress while increasing mitochondrial biogenesis.
2) A year later, research published in the journal Molecular Medicine Reports found that ivermectin preferentially targets stem cell population in MDA-MB-231 human breast cancer cells.
“Ivermectin has been demonstrated to be safe, following treatment of millions of patients with onchocerciasis and other parasitic diseases, which makes it a strong candidate for further studies investigating its potential use as a repurposed drug for cancer therapy,” reported the National Cancer Institute in Mexico City.
3) Another study published that same year in the American Journal of Cancer Research, also out of Mexico, determined that ivermectin is “a strong candidate for repositioning” as an anti-tumor remedy.
4) An earlier study published in EMBO Molecular Medicine back in 2014 similarly found that ivermectin inhibits the expression of WNT-TCF targets, which are implicated in both intestinal and lung cancers.
Ivermectin selectively inhibits TCF-dependent, but not TCF-independent, xenograft growth without causing any obvious side effects.
“In vivo, Ivermectin selectively inhibits TCF-dependent, but not TCF-independent, xenograft growth without obvious side effects. Given that Ivermectin is a safe anti-parasitic agent used by 200 million people against river blindness, our results suggest its additional use as a therapeutic WNT-TCF pathway response blocker to treat WNT-TCF-dependent diseases including multiple cancers,” researchers wrote.
Ivermectin works wonders against cancers of all types
5) In 2020, research published in Pharmacological Research identified ivermectin as a drug that promotes the death of cancer cells by regulating the tumor micro-environment in breast cancer.
Ivermectin also preferentially targets leukemia cells at low concentrations while leaving normal hematopoietic cells alone. The drug also targets various ovarian cancer cells lines and also inhibits the proliferation of five renal cell carcinoma cell lines without affecting normal kidney cells.
6) Also in 2020, a study published in the EPMA Journal found that ivermectin hits specific targets in ovarian cancer, suppressing ovarian cancer cells. The drug worked so well that researchers said it can be used to make personalized drug therapy, also known as predictive, preventive, and personalized medicine (PPPM), for ovarian cancer.
7) Researchers from the Instituto Nacional de Cancerologia in Mexico City discovered that same year that ivermectin reduces both cell viability and colony formation capacity while fighting against tumors.
8) In 2021, research published in the journal Frontiers in Pharmacology concluded that ivermectin increases ROS production and inhibits the cell cycle in the S phase to inhibit colorectal cancer cells.
9) Also in 2021, research published in the journal BMC Cancer found that ivermectin inhibits the proliferation of esophageal squamous cell carcinoma (ESCC) cells by inducing mitochondrial dysfunction, suppressing NF-?B signaling and promoting apoptosis.
As you can see, ivermectin is something of a wonder drug when it comes to cancer. This is precisely why it is off-limits, and why Americans need to speak out and start demanding access to this inexpensive, life-saving medication.
More related news coverage can be found at Cancer.news.
Ivermectin: An Effective Remedy Against Various Diseases: A Literature Review
Ivermectin was used as an antiparasitic agent upon discovery, but the present status of the drug is vague due to its huge effects on very wide range of diseases and pathogens. To the best of our knowledge, ivermectin can be used to treat and control viruses, bacteria, parasites, and cancer. Ivermectin provides new promising oppor-tunities to control and prevent a completely new range of diseases, thus generating global interest in evaluating and conducting researches on this wonder drug. Further studies are needed to introduce new targets and mecha-nism of the disease; thus the effects of this marvelous medicine may gain more prominence
- Ivermectin, a potential anticancer drug derived from an antiparasitic drug; Mingyang Tang, Xiaodong Hu et al; Pharmacol Res; 2021 Jan; 163: 105207;
- Ivermectin is a specific inhibitor of importin α/β-mediated nuclear import able to inhibit replication of HIV-1 and dengue virus; Wagstaff K.M., Sivakumaran H., Heaton S.M., Harrich D., Jans D.A. Biochem J. 2012;443(3):851–856.
- Flavivirus: From Structure to Therapeutics Development; Rong Zhao, Meiyue Wang, Jing Cao, Jing Shen, Xin Zhou, Deping Wang, and Jimin Cao; Life (Basel) 2021 Jul; 11(7): 615.
- Ivermectin is a potent inhibitor of flavivirus replication specifically targeting NS3 helicase activity: new prospects for an old drug; Mastrangelo E., Pezzullo M., De Burghgraeve T., Kaptein S., Pastorino B., Dallmeier K., de Lamballerie X., Neyts J., Hanson A.M., Frick D.N., Bolognesi M., Milani M. J Antimicrob Chemother. 2012;67(8):1884–1894.
- Comparative study of the interaction of ivermectin with proteins of interest associated with SARS-CoV-2: A computational and biophysical approach; Lenin González-Paz, María Laura Hurtado-León, et al; Biophys Chem; 2021 Nov; 278: 106677.
- Antitumor effects of the antiparasitic agent ivermectin via inhibition of Yes-associated protein 1 expression in gastric cancer; Nambara S., Masuda T et al; Oncotarget. 2017;8(64):107666–107677.
- Dysregulated YAP1/TAZ and TGF-beta signaling mediate hepatocarcinogenesis in Mob1a/1b-deficient mice; Nishio M., Sugimachi K.et al; Proc Natl Acad Sci 2016;113(1):71–80.
- Ivermectin has New Application in Inhibiting Colorectal Cancer Cell Growth; Shican Zhou, Hang Wu et al; Front Pharmacol, 2021 Aug 13;12:717529
- Parasite Killer Ivermectin stops cancer drug resistance
- Anti-parasite drug ivermectin can suppress ovarian cancer by regulating lncRNA-EIF4A3-mRNA axes; EPMA Journal; 2020 May 28;11(2):289-309.
- Ivermectin reverses the drug resistance in cancer cells through EGFR/ERK/Akt/NF-κB pathway; Lu Jiang et al; J Exp Clin Cancer Res 38, 265 (2019).
- Ivermectin and cancer – https://www.cancertreatmentsresearch.com/ivermectin-in-oncology/
- Continuous high-dose ivermectin appears to be safe in patients with acute myelogenous leukemia – https://www.tandfonline.com/doi/abs/10.1080/10428194.2020.1786559?journalCode=ilal20
You can order Ivermectin, Mebendazole, Febendazole and Nitazoxanide here
Febendazole, Ivermectin, Nitazoxanide and Mebendazole are all powerful anti-cancer drugs that have been proven to be effective in treating a variety of cancers.
They work by targeting cancer cells (parasites) and preventing them from growing and spreading by stopping their uptake of glucose.
With their high success rate and minimal side effects, They are an excellent choice for those looking for a safe and effective treatment for cancer. Contact your oncologist and tell him about the studies showing the efficacy of these drugs.
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Dissolution of Spike Protein by Nattokinase
Holy Grail of COVID-19 Vaccine Detoxification
By Peter A. McCullough, MD, MPH
Far and away the most common question I get from those who took one of the COVID-19 vaccines is: “how do I get this out of my body.”
Nattokinase is an enzyme is produced by fermenting soybeans with bacteria Bacillus subtilis var. natto and has been available as an oral supplement. It degrades fibrinogen, factor VII, cytokines, and factor VIII and has been studied for its cardiovascular benefits.
Out of all the available therapies I have used in my practice and among all the proposed detoxification agents, I believe nattokinase and related peptides hold the greatest promise for patients at this time.
NOW Supplements, Nattokinase 100 mg (from Non-GMO Soy)
Degradative Effect of Nattokinase on Spike Protein of SARS-CoV-2
Immunofluorescence analysis showed that S protein on the cell surface was degraded when nattokinase was added to the culture medium. Thus, our findings suggest that nattokinase exhibits potential for the inhibition of SARS-CoV-2 infection via S protein degradation.
Excel Well LLC Professional Nutracueticals Fullscript dispensery is registered to accept Health Savings Account (HSA) and Flexible Spending Account (FSA) debit cards on all supplement orders
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Information on Beta blockers for anxiety
Here is an audio program on eliminating negative self talk. Negative thoughts plays a huge part in anxiety and getting stuck on them is called “rumination”. Stress increases histamine and chronic high histamine can cause OCD and rumination. Check out our page on mental health
Here is a website on doing a parasite cleanse.
But you should contact a medical doctor or a naturapathic doctor especially if you have cancer or Multiple Sclerosis before starting removal of the parasites.
This site is not designed to and does not provide medical advice, professional diagnosis, opinion, treatment or services to you or to any other individual. Through this site and linkages to other sites, I provide general information for educational purposes only. The information provided in this site, or through linkages to other sites, is not a substitute for medical or professional care, and you should not use the information in place of a visit, call consultation or the advice of your physician or other healthcare provider. I am not liable or responsible for any advice, course of treatment, diagnosis or any other information, services or product you obtain through this site.