Author Archive

First Cancer Protocol using Ivermectin, Mebendazole, and Fenbendazole Published

**UPDATE**

Recently, a previously declassified CIA document  has gone viral.  The doc summarizes a Soviet scientific paper that showed researchers believed parasites and cancer thrived under nearly identical metabolic conditions and accumulated large reserves of glycogen, a form of stored energy.

  • Myracyl D, Miracel D, Lucanthone, was reportedly effective against bilharzia parasites as well as cancerous growths. It has never been approved for medicinal use as chemo and has been tested in human clinical trials and is used in research. It is no longer commonly used in humans due to hepatotoxicity.[4]
  • Other compounds were found to interfere with nucleic acid production, a process essential for the uncontrolled growth of cancer cells.

It’s important to note that the document did not directly state that cancer was caused by parasites, only that there are biochemical similarities; however, this further proves why drugs like ivermectin, Mebendazole and Fenbendazole are helping cancer patients.

Go here to listen to an interview with Dr. Lee Merritt on how historical experiments showed parasites could induce stomach cancer in animals eating a high sugar diet or were vaccinated. She also questions how diet, vaccination and parasite susceptibility might intersect.

Since the paper below was published, there’s only been more success using repurposed drugs.  Also, a 2021 patent by Johns Hopkins University was unearthed for glioblastoma therapy using Mebendazole.

If you like getting information via video, go here for a 6 minute summary of the following paper.

https://isom.ca/article/targeting-the-mitochondrial-stem-cell-connection-in-cancer-treatment-a-hybrid-orthomolecular-protocol/

Targeting the Mitochondrial-Stem Cell Connection in Cancer Treatment: A Hybrid Orthomolectular Protocol

Ilyes Baghli1, William Makis2, Paul E. Marik3, Michael J. Gonzalez4,5,6, William B. Grant7, Ron Hunninghake8, Thomas E. Levy8, Homer Lim9, Richard Z. Cheng10, Igor Bondarenko11, Paul Bousquet12, Roberto Ortiz13, Mignonne Mary14, Dominic P. D’Agostino15, Pierrick Martinez16

Date of Publication: 19 September 2024

Abstract

The mitochondrial-stem cell connection (MSCC) theory suggests that cancer originates from chronic oxidative phosphorylation (OxPhos) insufficiency in stem cells. This OxPhos insufficiency leads to the formation of cancer stem cells (CSCs) and abnormal energy metabolism, ultimately resulting in malignancy. This concept integrates two well-established theories: the cancer stem cell theory and the metabolic theory. Drawing on insights from molecular biology, pharmacology, and clinical studies, this manuscript introduces a hybrid orthomolecular protocol targeting the MSCC. The protocol includes 7 therapeutic recommendations, consisting of orthomolecules, drugs, and additional therapies. The aim of this hybrid orthomolecular protocol is to achieve additive and synergistic effects to enhance OxPhos, inhibit the primary fuels of cancer cells (glucose and glutamine), target CSCs and metastasis. Thus, numerous experiments suggest that targeting MSCC could be a potential therapeutic approach for cancer treatment.  (See link for study)

_________________

http://

Fenben For Cancer Case Presentations

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.

As to cancerevery cancer registry in the world is up with new cases and documented rapid progression of disease aptly termed “turbo cancer.” Cases are up by 2.5X in New York state Medicaid vs. a 2017-2019 baseline, and The American Cancer Society states that this year the number of newly diagnosed cases of cancer will surpass  the 2 million mark for the first time ever.

The trendline went up with the rollout of genetic COVID-19 injections.

And it’s not like the FDA didn’t know.  The Moderna patent explains that when a foreign DNA sequence integrates with a host organism’s genome, it could lead to the activation of oncogenes, mutated genes that have the potential to cause cancer, or the inhibition of tumor suppression genes.  Researchers in the U.S. and Canada recently found DNA fragments in COVID-19 mRNA shots.

Go here for a review of a study that shows repeated injections of mRNA COVID-19 injections are taking down immune surveillance for nascent malignant cells while at the same time inducing autoimmunity.  

How was this allowed to happen?

Manufacturers skipped preclinical oncogenicity studies.

The COVID shots are highly contaminated with plasmidsSV40 sequences that have been linked to cancer, metals, PEG, nanotechnology, lipid nanoparticles, black particles, white floating matter, impurities from human fetal cell lines, hexagonal crystalline structures, parasites and eggs, and a hydra-like moving, self aware organisms.

But, according to the CDC, more than 240 billion dollars will be spent on cancer care in the United States on a yearly basis by 2030.  Just think about that.  That is close to a quarter of a trillion dollars going into the pockets of certain people and organizations.

Go here to download for FREE Dr. Marik’s entire book: Cancer Care: The Role of Repurposed Drugs and Metabolic Interventions in Treating Cancer, as well as webinar slides, cancer care summary, FLCCC cancer study, and also watch numerous videos.  You know an expert is serious when they make their hard work available for all at no cost.

For more:

http://  Scroll to 7:30

Ivermectin for Cancer

Oct. 12, 2024

Listen to Dr. Kathleen Ruddy, surgeon, researcher, and author on how ivermectin not only works for COVID but has 20 years of research showing its potential for cancer.  She met a previously healthy patient who ran marathons with no family history of cancer, but who developed stage 4 prostate cancer after being forced to get two Pfizer shots to keep his government job.  Under another doctor he did 9 months of radiation and chemotherapy only to be told, there’s nothing more to be done, go home and prepare to die.  At this point Ruddy met him and suggested he try ivermectin as she knew it wouldn’t hurt him and might help.  He drove to Tennessee where he paid cash for it as it was an over-the-counter drug there.  A few months after taking it he had his PSA checked which went from in the hundreds to 1.3 which is considered normal.  Nine months later he’s out dancing 3 nights a week for four hours.  A scan showed 3 of the four bone masses are gone.  

Lyme Testing Update, Alpha Gal Syndrome, and More Podcast

http://

Lyme Disease Testing Update, Alpha Gal Syndrome, and More With Global Lyme Alliance Leaders

Sept. 9, 2024

Fred Diamond’s popular book, “Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know” offers those who love someone with persistent or chronic Lyme disease ideas and tips to support this beloved person. It also helps Lyme survivors know how to ask for support.  The e-version of Fred’s book is always free for Lyme survivors. Just reach out to Fred on Facebook or LinkedIn. The print copy can be ordered at https://www.amazon.com/Love-Hope-Lyme….

On today’s episode, we discuss Alpha Gal Syndrome, a tick-borne disease that caused red meat allergies, Lyme testing updates, and new treatments in the works. His guest is Global Lyme Alliance CEO Laura MacNeill and then GLA Chief Scientific Officer Tim Sellati. They discuss the work GLA is doing to develop better diagnostics, tests and treatment for tick-borne diseases including Lyme and the coinfections Bartonella and Babesiosis.

They discussed work they are funding with Dr. Brandon Jutras at Northwestern University and other research projects in the Lyme and chronic illness world. When Fred was doing the research for his popular book “Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know,” he was ignorant about the work happening at universities to find better diagnostics, treatment, and mental health solutions for the millions of chronic Lyme disease survivors around the globe. If someone you love has been afflicted with Lyme disease, watch this podcast now.

If you have Lyme disease, listen for ways to get the support you need.

Investigations of Medical Cover-Ups & Pharma Scandals

https://rumble.com/v5gv4fd-sharyl-attkisson-my-investigations-of-medical-cover-ups-and-pharma-scandals.html Video Here (Approx. 50 Min)

Sharyl Attkisson: My Investigations of Medical Cover-Ups and Pharma Scandals

Sep-26-2024

Sharyl Attkisson is an investigative journalist and the Emmy Award-winning host of “Full Measure.” She is also the author of several books, including, most recently, “Follow The Science: How Big Pharma Misleads, Obscures, and Prevails.”

“Why am I as a non-medical reporter unearthing stories that this whole industry of medical and science reporters are not unearthing?” she asks.

In this episode, we dive into the problem of scientific and medical corruption, and how Attkisson’s eyes were opened to the dangers of blindly believing every establishment narrative about our health.

“The federal government/pharmaceutical industry have learned how to take our taxpayer money, legally launder them through universities—public and private, who then say they don’t have to reply to your FOIA requests or turn over any data, who then put out studies that are little more than narratives and propaganda that go unchallenged,” says Attkisson.

“The health of the individual and their informed consent is far paramount to what you think you are doing for the good of mankind. You don’t have the right, as a researcher, to say, ‘I can sacrifice this child or I can sacrifice something about informed consent because I think I have a more noble goal.’ That’s not your right.”

For more:

The ‘Remdesivir Papers’: NIH COVID Panel Learned Zilch & 12 Policies Must Be Changed For Health Freedom

https://childrenshealthdefense.org/defender/remdesivir-papers-drug-military-members-941-deaths/?

‘Remdesivir Papers’ Allege Controversial Drug Used to Treat Service Members Led to 601 Deaths

A military whistleblower released a series of documents revealing that the military began “liberally” administering remdesivir to service members who were suspected of having COVID-19 — months before the FDA approved the drug.

remdesivir bottle and stack of files

A military whistleblower released a series of documents revealing 601 deaths of military service members and a high rate of serious adverse events in clinical trials involving remdesivir, an antiviral commonly administered to COVID-19 patients during the pandemic.

According to “The Remdesivir Papers,” some clinical trials were improperly run. In the case of at least one study, results were never made public. The whistleblower also alleged a widespread lack of informed consent for trial participants.

“Data derived from the Department of Defense [DOD] Joint Trauma System … by a military whistleblower offers a stark contrast to results of multiple clinical trials involving the liberal usage of remdesivir in military treatment facilities and other civilian facilities, as well as its potential contribution to, at minimum, hundreds of untimely deaths,” the documents state.

Yet according to the documents, the military began “liberally” administering remdesivir to service members who were suspected of having COVID-19 — months before the U.S. Food and Drug Administration (FDA) approved the drug.

The whistleblower, known by the pseudonym Daniel LeMay, shared the documents with investigative journalist J.M. Phelps, who published them last week in The Gateway Pundit.

In interviews with The Defender, LeMay and Phelps discussed the documents and their significance.  (See link for article)

Important excerpt:

Former victims of the COVID-19 hospital protocols, which included administration of remdesivir, and advocates for those victims welcomed the documents’ release.

________________

**Comment**

This needs to go public. Public officials need to be held to account for the fraudulent ‘trials’ of ivermectin and hydroxychloroquine in order to preclude their use, making remdesivir the standard of care despite the obvious data showing that it kills people.  More whistleblowers need to come forward.

Gulick et al, published a “lessons learned” paper in Annals of Internal Medicine and missed the point entirely regarding ivermectin which exceeded all other drugs. Doctors and patients are finding success with ivermectin in combination with other nutraceuticals and drugs.  To make matters worse, the NIH guidelines advised against using ivermectin, which impeded doctors on the front line who found it effective and a part of community standard of care.

I highly recommend reading COVID ‘vaccine’ science catching up with ‘conspiracy theorists.’  Important excerpt:

Of course, while the science is starting to catch up, and the lawsuits are continuing apace (source), we’re still being told by our governments and mainstream media to roll up our sleeves, even those of us as young as 6 months. Source and source.

Okay then.

I’m with Dr. Vinay Prasad who once again candidly reiterates ‘mistakes were not made,’ and there should be no amnesty for COVID tyrants who are still lying.

Not only are they still lying, untold numbers of doctors have been persecuted by The Machine for simply doing their jobs and treating people.  Many lost their medical licenses and can no longer practice medicine.  This too has not been admitted or rectified by The Establishment.

https://childrenshealthdefense.org/defender/12-policies-need-change-true-health-freedom/?

These 12 Policies Need to Change If We Want True Health Freedom

In a free and moral society, health freedom is not simply a convenience — it’s an imperative.

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website.
statue of liberty and hand holding stethoscope

As a requirement for discussing and appreciating the imperative of health freedom in the U.S., we must first define what is meant by health freedom.

A simple definition is the right of every American to decide what medical interventions to put into or onto one’s body, the right to access and use the medical and healing modalities of one’s choice, the right to maintain one’s health according to one’s conscience and the right to live free of involuntary medication be it via the food supply, the water supply or something airborne.

In a free and moral society, health freedom is not simply a convenience; it’s an imperative.

In this vein, in the event of injury or illness, all Americans must possess the absolute right to choose what medical interventions and treatments to accept and what medical or healing modalities to utilize in order to address illness or injury; Americans must be free to choose how to maintain their health whether that be through nutrition, supplements, herbs, drugs or a myriad of healing modalities; Americans must have access to truthful information regarding how the seeds for plants and animal feed and the food in our food supply has been grown or developed, medicated, processed and packaged; and Americans have the right to exist in a society free of water and airborne medications, insect vectors and chemicals.

Health freedom can only exist in a free and moral society that values each and every member of that society. This prerequisite thus excludes medical mandates of any kind. It is immoral to force another individual to risk their life for the theoretical benefit of another.

Moreover, the government does not have the moral authority or power to dictate what medical products any American puts into or on his or her body. If anyone in government does possess that power, then no American is truly free, nor does he or she possess any meaningful right whatsoever — Americans are merely chattel.

In order to create a society based on true health freedom, the following policy shifts should be implemented, as a first step. There are many more changes that should be implemented as well, but these proposals would address some of the most glaring, pernicious anti-liberty and anti-health aspects of our system as it exists today:

1. Ban all medical mandates

The Declaration of Independence states, “that all men are created equal, that they are endowed by their Creator with certain unalienable Rights, that among these are Life, Liberty and the pursuit of Happiness.” Medical mandates are prima facie violations of our founding documents.

Health freedom demands prior voluntary informed consent before a medical treatment or intervention is administered. Medical mandates are thus, by definition, antithetical to voluntary consent and therefore must be prohibited in a free and moral society.

No single individual in government knows the medical history of any American, knows what is best for Americans, or has to live with the repercussions of any choices made by Americans, thus, medical mandates are never justified in any circumstance.

2. Repeal the Bayh-Dole Act

“The Bayh-Dole Act, formerly known as the Patent and Trademark Act Amendments, is a federal law enacted in 1980 that enables universities, nonprofit research institutions and small businesses to own, patent and commercialize inventions developed under federally funded research programs within their organizations.”

Under this program, government scientists may receive up to $150,000 per year on their patents.

In theory, Bayh-Dole incentivizes bright scientists to seek employment at federal health agencies rather than entering more lucrative private industry by allowing these taxpayer-funded scientists and other individuals and entities to retain the patent rights to intellectual property developed during their taxpayer-funded research and development activities.

In practice, this Act forever realigned the interests of taxpayer-funded scientists away from the American people and toward their own interests and profits and the profits of the private industries with which they collaborate.

Dr. Anthony Fauci and his team at the National Institute of Allergy and Infectious Diseases infamously owned half of the Moderna COVID-19 vaccine patent which incentivized the misguided COVID-19-era policies leading to a colossal violation of the rights of Americans demonstrating the perverse incentives created by Bayh-Dole and the necessity of repealing the act.

3. Repeal the Prescription Drug User Fee Act (PDUFA) of 1992

“The Prescription Drug User Fee Act (PDUFA) was created by Congress in 1992 and authorizes FDA [U.S. Food and Drug Administration] to collect user fees from persons that submit certain human drug applications for review or that are named in approved applications as the sponsor of certain prescription drug products. Since the passage of PDUFA, user fees have played an important role in expediting the drug review and approval process.”

In 2022 alone, the pharmaceutical industry paid $2.9 billion in user fees amounting to 46% of the FDA’s entire budget including $1.4 billion or 66% for their drug approvers’ salaries and $197 million or 43% of the biologics (vaccines) program budget.

As a direct consequence of PDUFA, the FDA has a vested interest aligned with the profits and success of the pharmaceutical industry rather than the health and well-being of the American people.

4. Repeal the Public Readiness and Emergency Preparedness Act (PREP Act) which authorizes the Secretary of the U.S. Department of Health and Human Services to issue a PREP Act declaration.

“The declaration provides immunity from liability (except for willful misconduct) for claims:

    • of loss caused, arising out of, relating to, or resulting from administration or use of countermeasures to diseases, threats and conditions
    • determined by the Secretary to constitute a present, or credible risk of a future public health emergency
    • to entities and individuals involved in the development, manufacture, testing, distribution, administration, and use of such countermeasures

“A PREP Act declaration is specifically for the purpose of providing immunity from liability, and is different from, and not dependent on, other emergency declarations.”

The PREP Act desecrates the ethical principle of informed consent by protecting individuals from liability even when they expressly act contrary to patients’ wishes and instructions and must be repealed.

5. Repeal the Affordable Care Act

The Affordable Care Act anchors Americans to the pharmaceutical and drug-based medical paradigm even though a majority of Americans used at least one form of “alternative” medicine in 2021 and spent $30.6 billion in out-of-pocket expenses for those holistic medicine services in 2023 according to Statista.

Instead, implement a health savings program that permits Americans to access the health and medical modalities of their choice which in turn would foster more competition and reduce the exorbitant healthcare costs in the U.S. by breaking the extant monopolies held by the medical and insurance industries.

6. Repeal the National Childhood Vaccine Injury Act (NCVIA)

NCVIA shields vaccine makers from liability (except for willful misconduct), creating a perverse incentive to industry to develop a never-ending stream of vaccines which are then mandated by the states.

Further, the NCVIA protects industry and vaccine programs by creating a separate administrative federal court structure lacking due process and discovery, managed by “Special Masters” instead of judges, all in violation of the constitutionally protected right to due process.

While NCVIA contains other provisions designed to protect American families and ensure the safety of the national vaccine supply, Congress is not conducting proper oversight and the promises made in 1986 at the time of the Act’s passage have not been upheld.

As such, Americans who have been injured or killed by vaccines are left with astronomical medical bills and to fend for themselves.

7. Prohibit private donations to government entities

Prohibit private individuals, foundations, corporations, contractors and any other person or entity from donating or otherwise giving money to any agency or entity of the federal government.

The FDA and the Centers for Disease Control and Prevention (CDC) accept money from private actors such as the Bill & Melinda Gates Foundation and Pfizer, thus skewing the interests of the agency in favor of these private actors and away from the American public.

Gates has collaborated with the FDA and the CDC Foundation takes money from the pharmaceutical industry whose products the CDC is responsible for monitoring for safety.

8. Cooling-off period for senior federal employees

Enact a five-year cooling-off period before which agency leadership, deputies and other key officials may depart federal agencies in order to enter the companies they regulate in the private sector.

9. Prevent conflicts of interest

Eliminate conflict-of-interest waivers so that no person serving on a health agency committee, board or other regulatory entity may have a conflict of interest. Disclosure of conflicts of interest is insufficient to ensure the agencies pursue the interests of the American people. Individuals with financial or ideological conflicts of interest should not serve as decision-makers in any capacity.

10. Prohibit government grants to nonprofits

Prohibit the government from allocating taxpayer dollars to nonprofits. Nonprofits exists to serve the public interests and should be funded directly by American citizens. If a nonprofit has a worthwhile mission, the public will gladly support it.

Government exists to protect our rights and should not be in the business of picking winners and losers nor should it be using third parties to pursue policies outside the reach and review of the public.

11. Ban water fluoridation

While water fluoridation programs are widespread, they are not only dangerous from a health standpoint, they are forced medication in violation of the ethical principle of informed consent.

Research comparing the health outcomes and IQs of communities that do and do not fluoridate their water supply reveals that children in the fluoridated water communities have reduced IQs and therefore inferior prospects in life. Other research has documented the health hazards of fluoride, an industrial waste product.

In addition, as fluoride is added to municipal water supplies, residents of those communities have no way to opt out and therefore are subjected to involuntary forced medication. No one should be forced to consume drugged water in order to maintain a biological necessity.

12. Ban the release of genetically modified insects

Two tenets of good health are abundant exposure to sunshine and fresh air; however, in some states, the state governments have collaborated with private businesses to release genetically modified mosquitoes into communities.

While these mosquitoes are often designed to breed with one another and eliminate the dangerous species going forward, the health impacts of humans being bitten by these insects are not well understood. Nor should a person have to risk being bitten by one of these creatures in order to venture outside. This amounts to a form of forced medication absent any form of consent and must be ended.

These recommendations should be understood as necessary first steps to begin correcting the disastrous health policy environment that exists in the U.S. today and to restore true health freedom in the U.S., which would allow all Americans to decide what medical interventions to allow into or onto one’s body, which health and medical modalities to utilize in maintaining their health and the ability to live free of involuntary medication be it via the food supply, the water supply or the air we breathe.

Originally published by Brownstone Institute.

Leslie Manookian is the president and founder of the Health Freedom Defense Fund. She is a former successful Wall Street business executive. Her career in finance took her from New York to London with Goldman Sachs. She later became director of Alliance Capital in London running their European growth portfolio management and research businesses.

Borrelia burgdorferi: Methods and Protocols

https://link.springer.com/book/10.1007/978-1-0716-3561-2#about-this-book

Borrelia burgdorferi: Methods and Protocols

2024

  • Includes cutting-edge methods and protocols
  • Provides step-by-step detail essential for reproducible results
  • Contains key notes and implementation advice from the experts

About this book

This volume covers the latest advancements and techniques used to understand the fastidious bacterium, Borrelia burgdorferi, and its significance in infectious disorders by combining both conventional and cutting-edge approaches. This book covers diverse topics, including direct detection, diagnostic methods, immune response analysis, alternative model systems, advanced proteomics, social media analysis, and clinical research. It also discusses unconventional wet lab research such as content analysis, the use of ChatGPT, clinical algorithms for chronic Lyme, establishment of a pregnancy Lyme disease biobank, and investigates Lyme in pregnant women. Written in the highly successful Methods in Molecular Biology series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls.

Cutting-edge and comprehensive, Borrelia burgdorferi: Methods and Protocols encompasses a wide range of techniques and caters to scientists from various disciplines and career stages, such as cell and molecular biologists, statisticians, and clinical researchers.