Using Herd Immunity Excuse for Gene Therapy Vaccine on Kids

In children and young adults from age birth to 19, the survival rate of COVID-19 is 99.997%.1,2 In most cases, symptoms are mild or nonexistent. Among children who were hospitalized, 0.19% of children died from COVID-19, with researchers concluding in a 2021 study, “Hospitalization and in-hospital death are rare in children diagnosed with COVID-19.”3
Despite the fact that COVID-19 has had little impact, physically, to children, health officials are setting the stage for widespread vaccination of this population. The University of Oxford, which is collaborating on a COVID-19 vaccine with AstraZeneca, is already enrolling children between the ages of 6 years and 17 years and 8 months in their U.K. vaccine trial.4
A COVID vaccine for infants and children is every bit as unnecessary, dangerous and foolish as the hepatitis B vaccine is for infants that I have been railing against for the past two decades.
Moderna is also enrolling 3,000 children between the ages of 12 and 17 to test their COVID-19 vaccine, using the same dose given to adults,5 while Pfizer also expanded its clinical trials to include children as young as 12.6 Johnson & Johnson even announced on February 28, 2021, that it plans to test its COVID-19 vaccine on infants, including newborn babies, pregnant women and people with compromised immune systems.
“They did not get into a lot of detail about it but did make it clear they will be pursuing pediatric and maternal coronavirus immunization studies,” Dr. Ofer Levy, a member of the FDA’s advisory committee who reviewed Johnson & Johnson’s vaccine data, told The New York Times.7
It’s Gene Therapy — Not a Vaccine

The COVID-19 vaccine really isn’t a vaccine in the medical definition of a vaccine. It’s more accurately an experimental gene therapy, of which the effectiveness and safety are far from proven. During the first six weeks the vaccine was available, more than 500 post-vaccination deaths and nearly 11,000 other adverse events were reported to the U.S. Vaccine Adverse Event Reporting System (VAERS).8
According to Children’s Health Defense (CHD), professor Dolores J. Cahill, Ph.D., a molecular biologist and immunologist, “expects to see successive waves of adverse reactions to the experimental messenger RNA (mRNA) injections ranging from anaphylaxis and other allergic responses to autoimmunity, sepsis and organ failure.”9
Considering that children are at extremely low risk from COVID-19, vaccination offers them far more risk than benefit, and parents may be understandably reluctant to volunteer their children to receive this experimental and unlicensed gene therapy. Public health officials have made it clear, however, that vaccination of children is expected. CHD reported:10

“Already last April — when next to nothing was known about COVID’s epidemiology, and candidate vaccines had barely begun to be studied — Bill Gates set the stage for the pediatric push, declaring that the end goal is to make COVID-19 vaccines ‘part of the routine newborn immunization schedule.’”

Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases (NIAID), also stated that 85% to 90% of the U.S. population, including children, will need to receive a COVID-19 vaccine before life can return to normal, and he suggested that first graders may be authorized to be vaccinated by September 2021.11
Using ‘Herd Immunity’ to Justify Vaccinating Children

Since children themselves have little reason to get a COVID-19 vaccine, health officials are spinning the notion that children must be vaccinated for the sake of herd immunity. Now, they want you to think that not only should you look at the people around you as vectors of disease, but also the children, who could be asymptomatic carriers, silently bringing a deadly disease to grandma’s house.
What’s being largely ignored, however, are the studies showing that children are not driving the COVID-19 pandemic and, in fact, appear less likely to transmit COVID-19 than adults.12
“In short, public health leaders say, parents must ‘vaccinate the young to protect the old.’ Given the federal government’s estimate that one vaccine injury results from every 39 vaccines administered, it seems clear that officials expect children to shoulder 100% of the risks of COVID vaccination in exchange for zero benefit,” CHD noted.13
Herd immunity, which occurs when enough people acquire immunity to an infectious disease such that it can no longer spread widely in the community, is calculated using reproductive number, or R-naught (R0), which is the estimated number of new infections that may occur from one infected person.14
R0 of below 1 (with R1 meaning that one person who’s infected is expected to infect one other person) indicates that cases are declining while R0 above 1 suggests cases are on the rise. It’s far from an exact science, however, as a person’s susceptibility to infection varies depending on many factors, including their health, age and contacts within a community.
The initial R0 calculations for COVID-19’s HIT were based on assumptions that everyone has the same susceptibility and would be mixing randomly with others in the community. But a study published in Nature Reviews Immunology suggested that the herd immunity threshold for COVID-19 may need to be adjusted because children are less susceptible to the disease:15

“Another factor that may feed into a lower herd immunity threshold for COVID-19 is the role of children in viral transmission. Preliminary reports find that children, particularly those younger than 10 years, may be less susceptible and contagious than adults, in which case they may be partially omitted from the computation of herd immunity.”

COVID Gene Therapy May Not Prevent Transmission

Another point being largely ignored in the mainstream media is that it’s unknown if the COVID-19 vaccines prevent transmission, putting a major hole in the push for vaccine-driven herd immunity.
Unlike conventional vaccines, which use an antigen of the disease you’re trying to prevent, the COVID-19 injections contain synthetic RNA fragments encapsulated in a nanolipid carrier compound,16 the sole purpose of which is to lessen clinical symptoms associated with the S-1 spike protein, not the actual virus.
They do not actually impart immunity or inhibit transmissibility of the disease. In other words, they are not designed to keep you from getting sick with SARS-CoV-2; they only are supposed to lessen your infection symptoms if or when you do get infected.17,18
At a virtual press conference held by the World Health Organization (WHO) on December 28, 2020, WHO officials warned there is no guarantee that COVID-19 vaccines will prevent people from being infected with the SARS-CoV-2 virus and transmitting it to other people.19
In a New Year’s Day interview with Newsweek, Fauci reinforced the WHO’s admission that health officials do not know if COVID-19 vaccines prevent infection or if people can spread the virus to others after getting vaccinated.20
Although the U.S. Food and Drug Administration (FDA) granted Emergency Use Authorization (EUA) in December 2020 for Pfizer/BioNTech21 and Moderna22 to release their experimental mRNA vaccines for use in the U.S., the companies only provided evidence from clinical trials to demonstrate that their vaccines prevented mild to severe COVID-19 disease symptoms in vaccinated participants compared to unvaccinated trial participants.
The companies did not investigate whether the vaccines prevent people from becoming asymptomatically infected with the SARS-CoV-2 virus and/or transmitting it to other people.23,24
Meanwhile, if you or your child recovered from COVID-19 or had an asymptomatic case, you likely already have some level of protective immunity25 — another factor being largely ignored in the push to vaccinate children. In fact, trials suggested there’s no benefit to getting vaccinated among those who have been previously infected with COVID-19.26
Fauci’s Involvement With Medical Patents

While Fauci is not named on the patent of Moderna’s vaccine, the NIH has a 50% stake in it,27 and the recognition that would come with a successful vaccine launch would certainly include Fauci. NIH scientists may also collect royalties from vaccines they’re involved with.28
The video above, with David E. Martin, Ph.D., a national intelligence analyst, also goes into detail about Fauci’s involvement with medical patents. Martin has pointed out that even though Moderna “very clearly did not have the legal right, and they did not have the contractual rights, they didn’t have the licensing rights” required to enter into a federal contract, they were still somehow pushed to the front of the line by the NIH and Fauci.
In the Fauci/COVID-19 Dossier prepared by Martin, he describes multiple criminal violations he believes are associated with “COVID-19 terrorism,” including gain of function research that was carried out by NIAID in violation of an NIH moratorium. Part of the dossier also spells out some of Fauci’s patents in detail along with the NIAID’s “economic bonanza”:29

“Since the passage of the Bayh Dole Act (Pub. L. 96-517, December 12, 1980), federally funded research has been an economic bonanza for U.S. universities, federal agencies, and their selected patronage. For the first decade following Bayh Dole, NIH funding doubled from $3.4 billion to $7.1 billion. A decade later, it doubled again to $15.6 billion.

In the wake of September 2001, the National Institute for Allergy and Infectious Diseases (NIAID) saw its direct budget increase over 300% without accounting for DARPA funds of as much as $1.7 billion annually from 2005 forward. In 2020, NIH’s budget was over $41 billion.

What has become of the $763 billion of taxpayer funds allocated to making America healthier since inventors have been commercially incentivized? Who has been enriched? The answer, regrettably, is that no accountability exists to answer these questions. The NIH is the named owner of at least 138 patents since 1980.

The United States Department of Health and Human Services is the named owner of at least 2,600 patents. NIAID grants or collaboration have resulted in 2,655 patents and patent applications of which only 95 include an assignment to the Department of Health and Human Services as an owner.

… NIAID’s Director, Dr. Anthony Fauci is listed as an inventor on 8 granted U.S. patents. None of them are reported in NIAID, NIH, or GAO reports of active licensing despite the fact that Dr. Fauci reportedly was compelled to get paid for his interleukin-2 ‘invention’ — payments he reportedly donated to an unnamed charity.”

Conflicts Are Rampant

It’s worth noting that Moderna has no legal rights to a key patent for its vaccine delivery system, and company executives are among those who have dumped their stock. Both Moderna and the NIH are essentially engaged in patent infringement, as a core part of the technology — the lipid nanoparticle (LNP) technology that is part of the vaccine delivery system — belongs to a small Canadian biotech company called Arbutus.30
Moderna sought to invalidate the patent owned by Arbutus Biopharma, but lost the challenge at the end of July 2020.31 After losing the challenge, Moderna said their LNP technology is actually far more advanced than Arbutus’ and claimed “the LNP used to make mRNA-1273, its Covid-19 vaccine candidate, is not covered by the Arbutus patent.”32 “In short,” the Dossier notes:33

“… while Moderna enjoys hundreds of millions of dollars of funding allegiance and advocacy from Anthony Fauci and his NIAID, since its inception, it has been engaged in illegal patent activity and demonstrated contempt for U.S. Patent law.

To make matters worse, the U.S. Government has given it financial backing in the face of undisclosed infringement risks potentially contributing to the very infringement for which they are indemnified.”

Conflicts of interest are also rampant at NIH, where, since 2012, health researchers receiving federal funding have reported more than 8,000 significant financial conflicts of interest totaling at least $188 million.34 In 2006,35 evidence was also uncovered showing that 916 NIH researchers had secretly received royalty payments for drugs and other inventions while working for the government.
Fauci was among those who had “received tens of thousands of dollars in royalties for an experimental AIDS treatment they invented [interleukin-2]. At the same time, their office has spent millions in tax dollars to test the treatment on patients across the globe.”
While it appears inevitable that the experimental COVID-19 gene therapy injections will soon be pushed on children, considering the many unanswered questions and conflicts in place, some may prefer to put off getting vaccinated against COVID-19 for as long as possible while waiting for the real truth to emerge.


If Your Gums Bleed You Might Be Deficient in This

If your gums bleed easily when you brush your teeth, you may need more vitamin C, according to a study by University of Washington (UW) researchers.1 Bleeding gums can be a warning sign of periodontal disease, also known as gum disease, that results from infection and inflammation in your gums and the bone supporting your teeth.2 Your gums may bleed even during the early stages of the disease, known as gingivitis.

However, according to Philippe Hujoel, a dentist and professor of oral health sciences with the UW School of Dentistry, if your gums are bleeding the first thing you think about shouldn’t be brushing and flossing more — even though this is what the American Dental Association recommends — it should be figuring out why your gums are bleeding, and a nutrient deficiency could be to blame.3

Low Vitamin C Levels Linked to Bleeding Gums

The recommended daily vitamin C intake set by the World Health Organization was based on scurvy prevention, but according to the UW study, this may be too low to achieve the full benefits that vitamin C, also known as ascorbic acid, has to offer.4 One such benefit is the prevention of microvascular fragility, a condition that can manifest as bleeding gums or retinal hemorrhaging.

Using data from 15 trials spanning six countries, the researchers found that vitamin C supplementation reduced the tendency for bleeding gums in people with vitamin C levels below 28 ?mol/L. Vitamin C levels are considered normal when they’re greater than 28 ?mol/L, while vitamin C depletion is diagnosed at 11 to 28 ?mol/L and a deficiency at less than 11 ?mol/L.5

For those with vitamin C levels greater than 48??mol/L, vitamin C supplementation did not reduce bleeding gums in all cases. However, both retinal hemorrhaging and bleeding gums increased when vitamin C levels fell to the 11 to 28 ?mol/L range, which is considered adequate for protection against scurvy.6

They concluded that vitamin C requirements intended to prevent scurvy may lead to vitamin C levels in the body that are too low to prevent bleeding gums. Further, the tendency for bleeding gums and retinal hemorrhaging is associated with low vitamin C levels and could be an indication of systemic microvascular pathology, including bleeding in the brain, heart or kidneys,7 that could be reversed by increasing daily vitamin C intake.8

This isn’t the first time the link between vitamin C and gum bleeding has been discovered. Paul Robertson, the former dean of the UW School of Dentistry, conducted studies in 1986 and 1991 that also found a connection. According to the study’s lead author Philippe Hujoel:9

“There was a time in the past when gingival bleeding was more generally considered to be a potential marker for a lack of vitamin C. But over time, that’s been drowned out or marginalized by this overattention to treating the symptom of bleeding with brushing or flossing, rather than treating the cause.”

This is problematic, because by focusing only on brushing and flossing, the systemic damage caused by the nutrient deficiency continues. The study noted:

“A default prescription of oral hygiene and other periodontal interventions to ‘treat’ microvascular pathologies, even if partially effective in reversing gingival bleeding as suggested in this meta-analysis, is risky because it does not address any potential morbidity and mortality associated with the systemic microvascular-related pathologies.”

Why Your Body Needs Vitamin C

Vitamin C, a water-soluble vitamin found in abundance in fruits and vegetables, is an essential nutrient that humans must get from their diet or supplements. It has powerful antioxidant properties because of an ability to donate electrons to oxidized molecules.

Vitamin C, even in small quantities, protects proteins, lipids and even DNA and RNA in your body from reactive oxygen species that are generated during normal metabolism as well as due to toxin exposure, such as cigarette smoke and air pollution.

Vitamin C is also involved in the biosynthesis of collagen, carnitine and catecholamines, according to Rhonda Patrick, Ph.D., and as such, “vitamin C participates in immune function, wound healing, fatty acid metabolism, neurotransmitter production, and blood vessel formation, as well as other key processes and pathways.”10

Vitamin C’s anti-cold effects are also among its most-studied uses, and research suggests that using vitamin C prophylactically as well as therapeutically at the onset of cold symptoms may reduce symptoms and cold duration.11

It may also be useful against COVID-19 and, as noted by Dr. Andrew Saul, editor-in-chief of the Orthomolecular Medicine News Service, at extremely high doses vitamin C acts as an antiviral drug.

Oral Health Is Part of Your Overall Health

If your gums are bleeding or you’re having any other problem with your oral health, seeking the foundational cause is key, as what happens in your mouth doesn’t stay there.

“Your teeth are organs that are connected to your whole nervous system and basically are part of your brain, kind of like your eyes,” biological dentist Dr. Dominik Nischwitz said during our 2020 interview on holistic dental care. “You have this massive brain nerve there called the trigeminal nerve. It’s one of the 12 cranial nerves and takes up 50% of the space of all the other ones, so it’s quite important.”

While it’s true that brushing and flossing are important, they’re not going to correct a low vitamin C level, for instance, if that’s what’s causing your gums to bleed. Nischwitz also focuses on nutrition and has developed a Bone Healing Protocol that includes certain micronutrients and focuses on high doses of vitamin D3.

Vitamin D levels, for example, should ideally be above 60 nanograms per milliliter (ng/mL), and if your levels are low to begin with, you may need to take a supplement for several months before any further treatments begin. The protocol also stresses magnesium, vitamin K2, vitamin C and B vitamins.

Nutrients for Gum and Oral Health

Just as it’s important to optimize the bacteria in your gut, it’s important to optimize the bacteria in your mouth. Your oral microbiome is negatively affected by antibacterial mouthwash, fluoride-containing toothpaste and fluoridated water, so stopping the use of these items is the first step to a healthier mouth.

“In the mouth, you don’t want to have a ‘scorched earth policy,’ nuking all bacteria and hoping the good bugs come back,” says biological dentist Dr. Gerry Curatola, founder of Rejuvenation Dentistry. “[G]ood bugs basically have a harder chance of setting up a healthy-balanced microbiome when you disturb them, denature them or dehydrate them with alcohol-based products.”

Curatola describes your mouth as your “gateway to total body wellness” and is among those who recommend specific nutrients to support gum and overall health. In addition to vitamin C, he recommends coenzyme Q10 (CoQ10), as bleeding gums are often a sign of CoQ10 deficiency.

There are also a number of homeopathic tissue salts that can be beneficial for oral health, including silica, calcarea fluorica (calcium fluoride), calcium phosphate and calcium carbonate.

Oil Pulling for a Healthier Mouth, Reduced Bleeding

A gentle way to reduce plaque, bad breath and gingivitis while improving oral health and hygiene is oil pulling using coconut oil. According to Ayurvedic tradition, oil pulling may improve more than 30 systemic diseases including reduced inflammation and bleeding.12

While tending to your oral health via diet and lifestyle changes is essential, oil pulling is a sensible addition to your daily oral hygiene routine. Coconut oil is an ideal oil for oil pulling due to its antimicrobial effects.13 Coconut oil is antibacterial and antiviral and contains 92% saturated fats,14 49% of which is the anti-inflammatory and antimicrobial medium chain saturated fat lauric acid.15

It may also be effective against gingivitis. In a pilot study of 20 people with plaque-induced gingivitis, coconut oil was used as a mouthwash daily for 30 days. A control group carried out normal daily oral health procedures but without coconut oil. Both plaque and bleeding decreased in the groups, but the coconut oil group had a more significant decline, showing promise for reducing plaque formation and gingivitis.16

Another study also added coconut oil pulling to the normal oral hygiene procedures of middle-aged adults with plaque-induced gingivitis. The group that used oil pulling in addition to regular brushing had a significantly greater decline in gingivitis and plaque after six weeks.17

U.K. researchers also conducted a systematic review to look into the effect of oil pulling with coconut oil on oral health, finding that coconut oil pulling worked as well as chlorhexidine mouthwash for plaque score, gingival index score and bleeding-on-probing.18

The Best Way to Boost Your Vitamin C

If you struggle with bleeding gums, it’s essential to optimize your vitamin C levels. Certain populations, including people who smoke, consume alcohol or have inflammatory bowel disease, may need increased intake of vitamin C, but some research suggests vitamin C deficiency may be more common than realized.

“Interestingly, a population-based cross-sectional study of nearly 150 patients admitted to a large teaching hospital in Canada found that 60% of the patients had suboptimal plasma vitamin C levels and 19% were deficient, with levels approaching those associated with scurvy,” Patrick noted.19

Fortunately, a wide variety of foods are high in vitamin C, including red pepper, parsley, broccoli, kiwi, strawberries, guava, tomato and all citrus fruits. You can get significant amounts of vitamin C from your diet if you eat these foods on a daily basis. If you’re deficient or you want to treat illness, vitamin C in supplement form, either liposomal or IV, may be needed.


Is This Inhaler Effective for Respiratory Viruses?

Please understand I am only posting information to be complete as this is NOT in any way, shape or form my primary recommendation for the treatment of COVID-19. There is little to no doubt in my mind that the most effective and safest treatment for this illness is nebulized diluted hydrogen peroxide at .1% with one drop of either 5% Lugol’s iodine or 2 drops of the 2% concentration.
Dr. David Brownstein has successfully treated more than 230 COVID-19 patients using immune boosting strategies such as intravenous or nebulized hydrogen peroxide, iodine, oral vitamins A, C and D, and intramuscular ozone. None has died from the infection.
I’ve embraced nebulized peroxide since the COVID-19 pandemic broke out and have received many anecdotal reports from people who have successfully used it, even at more advanced stages.
Based on Brownstein’s experience, I now also recommend adding iodine when nebulizing, as it appears to make it even more effective. You can find the details of using nebulized peroxide for COVID-19 by watching my interview with Brownstein below. The video embedded in our interview is a more detailed explanation of hydrogen peroxide nebulization and how to do it.

Download Interview Transcript

Inhaled Steroid Treatments

During the early days of the COVID-19 pandemic, reports from China, Italy and the U.S. revealed something curious about patients hospitalized with COVID-19: Those with chronic respiratory diseases like asthma and chronic obstructive pulmonary disease were significantly underrepresented, according to a team of researchers from the University of Oxford.1
The team suggested this may be due to their widespread use of inhaled glucocorticoids, such as budesonide. Further, the onset of COVID-19 is typically mild, “giving a potential window to intervene prior to the development of severe disease,” they wrote in the preprint journal medRxiv. However, most studies have only focused on treating severe COVID-19 in hospitalized patients.
“There have been important breakthroughs in hospitalized COVID-19 patients, but equally important is treating early disease to prevent clinical deterioration and the need for urgent care and hospitalization, especially to the billions of people worldwide who have limited access to hospital care,” study author professor Mona Bafadhel said in a news release.2
The researchers conducted a randomized trial involving 146 people in order to determine if budesonide, when used early during COVID-19 infection, would improve outcomes, with promising results.
Early Inhaler Use for COVID-19 

Of the 146 people in the study, half took 800 micrograms of budesonide twice a day within seven days of the onset of COVID-19 symptoms while half received usual care.3,4 Inhaled budesonide lowered the relative risk of needing urgent care or hospitalization by 90% over 28 days, while also resolving fever and other symptoms faster and leading to fewer persistent symptoms during the study period.5
Specifically, those taking budesonide recovered one day sooner than those who didn’t; clinical recovery occurred after a median of seven days in the inhaler group compared to eight days among those receiving usual care.6 Persistent symptoms were lower in the inhaler group at both 14 and 28 days compared to the usual care group. Bafadhel noted:7

“Although not the primary outcome of study, this is an important finding. I am encouraged to see the reduction in persistent symptoms at 14 and 28 days after treatment with budesonide. Persistent symptoms after the initial COVID-19 illness have emerged as a long-term problem. Any intervention which could address this would be a major step forward.”

The researchers also calculated the number needed to treat, or NNT, which describes how many people have to take a particular drug to avoid one incidence of a medical issue. In this case, the NNT with inhaled budesonide to reduce COVID-19 deterioration was eight.8
For comparison, influenza vaccines have an NNT, or NNV (number needed to vaccinate) of 71,9 meaning 71 people must be vaccinated to prevent a single case of confirmed influenza. Vitamin D has an NNT of 33 in terms of preventing acute respiratory tract infections,10 although among those who were severely vitamin D deficient at baseline, taking vitamin D had an NNT of four.
The researchers concluded, “Early administration of inhaled budesonide reduced the likelihood of needing urgent medical care and reduced time to recovery following early COVID-19 infection.”11
Inhaler Treatment ‘Equivalent’ to COVID Vaccine Effectiveness

According to the University of Oxford team, the main reason why people with asthma and COPD use inhaled glucocorticoids is to reduce exacerbations in their conditions, which are often caused by viral infections.
Studies in-vitro have previously shown that such inhalers reduce the replication of SARS-CoV-2, the virus that causes COVID-19, in airway epithelial cells.12 Airway epithelial cells act as the second line of defense after the mucus layer, acting as a physical barrier within your respiratory tract.
Inhaled glucocorticoids may also downregulate the expression of angiotensin converting enzyme-2 (ACE2) and transmembrane protease serine 2 (TMPRSS2), which play a role in the entrance of viruses into cells.13
A combination of drugs including budesonide has also been shown to inhibit the replication of coronavirus 229E, one cause of the common cold, by inhibiting receptor expression and may also help to modulate inflammation in the airways caused by the infection.14
The researchers noted that the 90% relative reduction in clinical deterioration seen after short-term use of budesonide is equivalent to the effectiveness of COVID-19 vaccines and greater than the effectiveness of any treatments currently used to treat hospitalized severely ill COVID-19 patients.
Further, in the event that mutated strains of SARS-CoV-2 become widespread, budesonide may have a notable advantage over vaccination, with researchers stating, “Unlike with vaccines, the efficacy of inhaled budesonide is unlikely to be affected by any emergent SARS-CoV-2 variant.”15
While there are some concerns about systemic effects of inhaled glucocorticoids when used long term, short-term use of the medications for purposes of treating COVID-19 may represent a relatively safe, low-cost and widely available intervention. According to the study:16

“The number of participants needed to treat to prevent increased health care resource utilization is 8, and combined with the short treatment period required to achieve benefit, makes this potentially an affordable and scalable intervention for early COVID-19.

This is especially significant in low- and middle-income countries where the majority of currently approved COVID-19 treatments are unlikely to ever reach patients as a consequence of variable healthcare systems.”

N-acetylcysteine (NAC) and Glutathione 

A number of other treatments have also shown promise for the treatment of COVID-19. N-acetylcysteine (NAC) and glutathione are among them. NAC is a form of the amino acid cysteine.
It is most well-known to help increase glutathione and reduce the acetaldehyde toxicity17 that causes many hangover symptoms. Anyone who overdoses on Tylenol also receives large doses of NAC in the emergency room, as it helps prevent liver damage by increasing glutathione.
The reason why NAC and glutathione are valued for COVID-19 is because of the role they play in combating oxidative stress, which is a main cause of inflammation and disease in general, and the cytokine storm associated with COVID-19 in particular. NAC may also combat the abnormal blood clotting seen in many cases.
Research has demonstrated that NAC can attenuate symptoms of influenza and improve cell-mediated immunity. In terms of influenza, according to pulmonologist Dr. Roger Seheult in a MedCram lecture,18 NAC has an NNT of 0.5, which means for every two people treated with NAC, one will be protected against symptomatic influenza.19
Additional Treatments for Respiratory Viruses

Many options exist for COVID-19 treatments, although not many of them are being widely publicized. Following is a sampling of some of the options being considered:

• Vitamin D — Research published in November 2020 in the Postgraduate Medical Journal, shows oral vitamin D supplementation also helps speed up SARS-CoV-2 viral clearance.20 More than 200 doctors, scientists and leading authorities have signed an open letter calling for increased use of vitamin D in the fight against COVID-19.21
• Vitamin C — While health authorities and mainstream media have ignored, if not outright opposed, the use of vitamin C and other supplements in the treatment of COVID-19, citing lack of clinical evidence, a landmark review recommends the use of vitamin C as an adjunctive therapy for respiratory infections, sepsis and COVID-19.22
The review detailed vitamin C’s mechanisms of action and how it helps in cases of infectious disease, including the common cold, pneumonia, sepsis and COVID-19. For starters, vitamin C has the following basic properties:23


While high-dose vitamin C regimens typically call for intravenous administration, if treating a viral infection at home (be it COVID-19 or something else), you could use oral liposomal vitamin C, as this allows you to take far higher doses without causing loose stools.
You can take up to 100 grams of liposomal vitamin C without problems and get really high blood levels, equivalent to or higher than intravenous vitamin C. I view that as an acute treatment, however. I discourage people from taking mega doses of vitamin C on a regular basis if they’re not actually sick, because it is essentially a drug — or at least it works like one.
• Hydroxychloroquine (HCQ) — HCQ, a so-called zinc ionophore and antimalaria, drug, has shown effectiveness against COVID-19. As early as March 2020, Dr. Vladimir Zelenko boasted a near-100% success rate treating COVID-19 patients with hydroxychloroquine (HCQ), azithromycin and zinc sulfate for five days.24 As of February 2021, Zelenko has treated 3,000 patients with COVID-19 symptoms and only three high-risk patients have died.
HCQ should be available to most people in the U.S. at this point, but you do need a prescription, and some doctors are still unwilling or resistant to prescribe it. If you can’t find HCQ, the nutritional supplement quercetin may be a useful (and perhaps even better) substitute, as its primary mechanism of action is identical to that of the drug. It also has antiviral activity of its own.
• Ivermectin — In December 2020, the Frontline COVID-19 Critical Care Alliance (FLCCC) called for widespread adoption of ivermectin, both as a prophylactic and for the treatment of all phases of COVID-19.25,26 In one trial, 58 volunteers took 12 milligrams of ivermectin once per month for four months.
Only four (6.96%) came down with mild COVID-19 symptoms during the May through August 2020 trial period. In comparison, 44 of 60 health care workers (73.3%) who had declined the medication were diagnosed with COVID-19.27

Early Treatment May Be Key

A common thread with many available treatments is that the earlier treatment starts, the better the outcomes tend to be. In the case of budesonide, for instance, treatment occurred within seven days of the onset of symptoms. In addition to early care, prevention is an even better option, and this is where strategies like vitamin D optimization become essential.
If you review my recent interviews with Drs. Brownstein and Zelenko you will learn that they have been in the trenches treating many with this illness and it has been their consistent observation that if this illness is treated early in the course of the disease you can virtually eliminate the risk of long term complications. So, the key is to treat early.


‘Digital Anti-Hate’ Group Puts Dr. Mercola on Hit List

As detailed in “Spy Agencies Threaten to ‘Take Out’ Mercola,” this website has been labeled a national security threat by British and American intelligence agencies that are collaborating to eliminate “anti-vaccine propaganda” from public discussion using sophisticated cyberwarfare tools.1,2,3
One of the public frontrunners in this comprehensive attack on my freedom of speech is a U.K.-based group with opaque funding called the Centre for Countering Digital Hate (CCDH), led by Imran Ahmed, a member of the Steering Committee on Countering Extremism Pilot Task Force under the British government’s Commission for Countering Extremism.
In its report, “The Anti-Vaxx Playbook,”4 the CCDH identifies me as one of the six most influential “anti-vaxxers” online that must be silenced for good. The other five are Barbara Loe Fisher, Del Bigtree, Robert F. Kennedy Jr., Sherri Tenpenny and Andrew Wakefield.
The CCDH also admits tracking and spying on 425 vaccine-related Facebook, Instagram, YouTube and Twitter accounts that, together, have 59.2 million followers.5
The CCDH has been one of the most vocal organizations calling for the deplatforming of anyone who might have the ability to influence public opinion about vaccines.6 This despite the fact that public discourse and debate is a requirement not only for a well-informed public but also to protect scientific integrity and public health.
Anti-Hate Group Publishes Digital Hit List

More recently, the CCDH published an updated hit list on Twitter,7 now listing the “Top 10 anti-vaxxers” it wants digital platforms to eradicate. The list shows, by way of crossing out names, which have already been successfully deplatformed, and from which social media.
As of March 3, 2021, Kennedy Jr. has been banned from Instagram, and the National Vaccine Information Center (NVIC), co-founded and led by Fisher, has been removed from Facebook.

“Facebook has removed the NVIC, another page spreading vaccine misinformation run by Barbara Loe Fisher,” CCDH said in its Tweet.8 “But Facebook has allowed the NVIC to carry on spreading misinformation on Instagram, which it owns. Facebook, it’s time for action across your platforms.”

Good News: People Are Seeing Through the Propaganda

The irony of an “anti-hate” group posting a hit list — the only purpose of which is to seed public outrage and hate against those listed — did not escape unnoticed, and that’s part of the good news. More and more people are indeed starting to see the 1984-style double-think propaganda for what it is.
As pointed out by one Twitter follower: “You’ve posted what appears to be a digital hit list. Do you not see anything ironic about this considering your brand is ‘countering digital hate’?” “Project much?” said another. A third replied back to the CCDH saying “You should be on this list,” and a fourth said “It appears that by the word ‘hate’ you include uncomfortable truths.” Other responders wrote:

“I have personally benefited from the free TRUE loving information that at least seven on your list have given me since 2011. I have only gratitude and love for them. No regular doctor could help me back then and thanks to the info I got I didn’t die and I have helped others too.”
“’Misinformation’ … what a joke!! These people are putting their careers and livelihoods on the line to share the TRUTH, to empower us to take our health in our own hands and realize it’s the only way!! This is more a top list of who to follow!!!”
“This is nonsense at the extreme. Censorship has gone mad and needs to be heavily questioned and stopped — this is what all dictators and extremists themselves do! How ironic! The CCDH are extremist dangerous hate criminals themselves for doing this!”
“Stop the censorship! We are seeing through this failed attempt to spread valuable information from people.”
“Congratulations to every hero on that list.”

I could keep going, but you can read the comments for yourself. I encourage you to do so if you feel downtrodden, thinking the dark side is winning the information war. They’re not, but they get an “A” for effort. We, in turn, cannot let up our own efforts to spread the truth. We must be just as persistent.
NVIC — The Latest Victim in the War on Truth

NVIC, the latest victim of the CCDH’s organized attack on the U.S. First Amendment, had maintained a Facebook page since 2008. The organization itself has been around for nearly four decades, and worked with the U.S. Congress to establish the 1986 National Childhood Vaccine Injury Act. Facebook deleted NVIC’s account March 2, 2021.
NVIC does not make recommendations when it comes to the use of vaccines, its sole aim being to “defend the ethical principle of informed consent to medical risk taking, including vaccine risk taking.” Part of that work includes publishing fully referenced information about vaccines so that consumers can make an informed decision either way.
If NVIC had not done such a good job educating the public about vaccination and health for four decades, our Facebook page would still be up. ~ Barbara Loe Fisher
Considering few doctors, and none of the pro-vaccine front groups, are transparent about reported side effects and science raising red flags, NVIC serves a truly crucial public health service. You simply cannot make an informed decision if you’re only ever told one side of the equation — the supposed benefit side — while potential adverse effects, which may be lifelong, are hidden or denied. As reported by independent journalist Sharyl Attkisson:9

“Far from a fringe group, as propagandists try to convince the public, Fisher has provided consumers with crucial vaccine safety information for decades and served as an appointed member of the U.S. Department of Health and Human Services on the National Vaccine Advisory Committee as part of the Vaccine Safety Writing Group, on the agency’s Vaccine Policy Analysis Collaborative, on the Blue Ribbon Panel on Vaccine Safety, and Chair of the Subcommittee on Vaccine Adverse Events.

Additionally, Fisher has served as a member of the FDA’s Vaccine and Related Biological Products Advisory Committee. And she has been a member of the National Academy of Sciences Institute of Medicine Vaccine Safety Forum.”

NVIC Responds to Deplatforming
In an official statement, Fisher responded to the deplatforming by Facebook saying:10

“We are not surprised that Mark Zuckerberg views the truthful information that NVIC publishes about vaccine science, policy and law as a threat to perpetuating false narratives about vaccine safety created by the pharmaceutical industry and its business partners.

The U.S Congress has encouraged the creation of public-private business partnerships between vaccine manufacturers and federal agencies for the past three decades.

In order to be part of those lucrative partnerships, Silicon Valley companies like Facebook are clearly happy to engage in censorship. If NVIC had not done such a good job educating the public about vaccination and health for four decades, our Facebook page would still be up.

NVIC encourages everyone to leave social media networks eroding civil liberties, which include freedom of thought, speech and conscience, and join those that protect freedom of speech.

To stay connected with NVIC, become a registered user of the free online NVIC Advocacy Portal and defend vaccine choices in your state; become a subscriber of our free NVIC Newsletter and free weekly journal digital newspaper, The Vaccine Reaction; and interact with our followers on MeWe, Telegram, Gab and Parler.”

Decentralized Uncensorable Web Is Part of the Answer

As more and more truth-tellers, public health watchdogs, civil rights advocates and investigative journalists are censored and deplatformed, it’s easy to get discouraged. However, there is light on the horizon. Part of the answer, apart from calling on our political representatives to take a firm stand against censorship at every turn, is the creation of a decentralized web.
I am currently working with some of the brightest minds in the tech space — cybersecurity experts and billionaire philanthropists who are very well networked. These individuals are committed to preserving your personal freedoms and liberties. We aim to redo of the entire internet by implementing a strategy proposed by Tim Berners-Lee.
For those of you who don’t know, Berners-Lee invented the world wide web graphical interface of the internet 30 years ago, and he didn’t take a penny for it. Had he licensed this technology, he surely would be the richest person in the world today.
You can read more about Berners-Lee’s plan in this February 5, 2021, article in The Conversation,11 but essentially, it focuses on maintaining data sovereignty, giving you control over your data and privacy and undoing the current system of surveillance capitalism where Big Tech profits off your personal data and uses it against you at the same time. In this Web 2.0, tech monopolies also will no longer have the ability to censor.
While you wait for a decentralized, censorship-free internet, I second Fisher’s suggestion to ditch all social media networks that erode your civil liberties, and to join those that promote freedom of speech instead.
For example, free-speech alternatives to Facebook and Twitter include Gab, MeWe, Minds and Parler. Uncensored alternatives to YouTube include Bitchute, Rumble, Brighteon, and Thinkspot.
For content creators and alternative news sources that no longer have a social media presence due to censoring, subscribe to their newsletter if available, and/or mark their website in your favorites and check back on a regular basis.
Take Control of Your Online Presence
Beyond that, consider safeguarding your own online privacy if you haven’t done so already. To encrypt your text messages and keep them from becoming data mining fodder, download the Signal or Telegram app and/or use a virtual private network (VPN) on your desktop, laptop and mobile devices.
Telegram has grown in popularity as many who have been banned on other social media platforms have migrated there. In addition to encrypting your text messages, the app also allows you to subscribe to channels. Read-only messages (although some also have the ability to comment) are sent to your phone from any channel you subscribe to.
Lastly, if you care about privacy and free speech, stop using any and all Google products, including its search engine, browser, email service, Google docs, Google Home devices, Fitbit and Android phones. There are alternatives to all of them.
For search, check out DuckDuckGo and SwissCows. For a browser, consider Brave or Opera. From a security perspective, Opera is far superior to Google Chrome and even includes a free VPN service. For encrypted email, sign up with ProtonMail, which is based in Switzerland. As for online document sharing, Digital Trends has published an article listing a number of alternatives to Google Docs.12


COVID-19 ‘Vaccines’ Are Gene Therapy

As calls for mandatory COVID-19 vaccination grow around the world, it’s becoming ever more crucial to understand what these injections actually are. The mRNA “vaccines” created by Moderna and Pfizer are in fact gene therapies.

 Interestingly enough, mainstream media, fact checkers and various industry front groups insist the gene therapy claim is bogus, even though every single detail about the vaccines shouts otherwise. Why are they spreading this disinformation? Why do they not want you to know what these injections actually are? 
mRNA ‘Vaccines’ Fulfill None of the Criteria for a Vaccine
To start, let’s take a look at some basic definitions of words. According to the U.S. Centers for Disease Control and Prevention, a vaccine is:1

“A product that stimulates a person’s immune system to produce immunity to a specific disease, protecting the person from that disease.”

Immunity, in turn, is defined as:

“Protection from an infectious disease,” meaning that “If you are immune to a disease, you can be exposed to it without becoming infected.”

That’s the medical definition. The legal definition, in the few cases where it has been detailed, is equally unequivocal:

Iowa code2 — “Vaccine means a specially prepared antigen administered to a person for the purpose of providing immunity.”
Washington state code3,4 — “Vaccine means a preparation of a killed or attenuated living microorganism, or fraction thereof …” The statute also specifies that a vaccine “upon immunization stimulates immunity that protects us against disease …”

These definitions, both medical and legal, present problems for mRNA “vaccines,” since:

mRNA injections do not impart immunity. Moderna and Pfizer both admit that their clinical trials aren’t even looking at immunity. As such they do not fulfill the medical and/or legal definition of a vaccine.
They do not inhibit transmissibility of SARS-CoV-2 infection. As such they do not fulfill the medical and/or legal definition of a vaccine.

Dictionaries Attempt to Rewrite Medical Terms
We should not be fooled by attempts to condition the public to accept redefined terms. As of February 2019, Merriam-Webster defined5 “vaccine” as “a preparation of killed microorganisms, living attenuated organisms, or living fully virulent organisms that is administered to produce or artificially increase immunity to a particular disease.” By February 26, 2021, they had updated the definition of “vaccine” to:6

“A preparation that is administered (as by injection) to stimulate the body’s immune response against a specific infectious disease:

a: an antigenic preparation of a typically inactivated or attenuated … pathogenic agent (such as a bacterium or virus) or one of its components or products (such as a protein or toxin)
b: a preparation of genetic material (such as a strand of synthesized messenger RNA) that is used by the cells of the body to produce an antigenic substance (such as a fragment of virus spike protein)”

Let’s be clear. Merriam-Webster does not dictate medical terminology. It can be used, however, to confuse people. For now, all medical dictionaries still show the traditional definition of vaccine,7 as Merriam-Webster did up until this year. That said, I would not be surprised if changes are made there as well, eventually, if the misrepresentation of COVID-19 mRNA vaccines is allowed to stand.
mRNA Therapy Doesn’t Satisfy Public Health Measure Directive
There’s also the issue of whether a gene therapy can be mandated, and this may hinge on it being accepted as a vaccine. The 1905 Supreme Court ruling in Jacobson v. Massachusetts8 essentially established that collective benefit supersedes individual benefit.

Since mRNA therapies do not render the immunized person immune, and do not inhibit transmission of the virus, they cannot qualify as a public health measure capable of providing collective benefit that supersedes individual risk, and therefore cannot be mandated.

Put another way, the ruling argues (although legal experts diverge on some of the finer details of its interpretation) that it’s acceptable for some individuals to be harmed by a public health directive as long as it benefits the collective. However, if vaccination is a public health measure meant to protect and benefit the collective, then it would need to accomplish two things:

Ensure that the vaccinated person is rendered immune from the disease.
Inhibit transmission of the disease from the vaccinated person to other individuals.

We’re now back to the original problem that mRNA therapies for COVID-19 do not accomplish either of these things. Since these gene therapies do not render the person immune, and do not inhibit transmission of the virus, they cannot qualify as a public health measure capable of providing collective benefit that supersedes individual risk.

On the contrary, the only one benefiting from an mRNA “vaccine” is the individual receiving the gene therapy, since all they are designed to do is lessen clinical symptoms associated with the S-1 spike protein.

In other words, they won’t keep you from getting sick with SARS-CoV-2; they are only supposed to lessen your infection symptoms if or when you do get infected. So, getting vaccinated protects no one but yourself. Since you’re the only one who will reap a benefit (less severe COVID-19 symptoms upon infection), the justification to accept the risks of the therapy “for the greater good” of your community is blatantly irrational.
Marketing mRNA Therapy as Vaccine Violates Federal Law
Since mRNA “vaccines” do not meet the medical and/or legal definition of a vaccine, referring to them as vaccines, and marketing them as such, is a deceptive practice that violates9 15 U.S. Code Section 41 of the Federal Trade Commission Act,10 the law that governs advertising of medical practices.

The lack of completed human trials also puts these mRNA products at odds with 15 U.S. Code Section 41. Per this law,11,12 it is unlawful to advertise “that a product or service can prevent, treat, or cure human disease unless you possess competent and reliable scientific evidence, including, when appropriate, well-controlled human clinical studies, substantiating that the claims are true at the time they are made.”

Here’s the problem: The primary end point in the COVID-19 “vaccine” trials is not an actual vaccine trial end point because, again, vaccine trial end points have to do with immunity and transmission reduction. Neither of those was measured.

What’s more, key secondary end points in Moderna’s trial include prevention of severe COVID-19 disease (defined as need for hospitalization) and prevention of infection by SARS-CoV-2, regardless of symptoms.13,14 However, Moderna did not actually measure rate of infection, stating that it was too “impractical” to do so.
That means there’s no evidence of this gene therapy having an impact on infection, for better or worse. And, if you have no evidence, you cannot fulfill the U.S. Code requirement that states you must have “competent and reliable scientific evidence … substantiating that the claims are true.”

Making matters worse, both Pfizer and Moderna are now eliminating their control groups by offering the real vaccine to any and all placebo recipients who want it.15 The studies are supposed to go on for a full two years, but by eliminating the control group, determining effectiveness and risks is going to be near impossible.
What Makes COVID Vaccines Gene Therapy?

Alright. Let’s move on to the definition of “gene therapy.” As detailed on’s “What Is Gene Therapy” page:16

“Gene therapy is an experimental technique that uses genes to treat or prevent disease … Researchers are testing several approaches to gene therapy, including: … Introducing a new gene into the body to help fight a disease …
Although gene therapy is a promising treatment option for a number of diseases (including inherited disorders, some types of cancer, and certain viral infections), the technique remains risky and is still under study to make sure that it will be safe and effective. Gene therapy is currently being tested only for diseases that have no other cures.”

Here, it’s worth noting that there are many different treatments that have been shown to be very effective against COVID-19, so it certainly does not qualify as a disease that has no cure. It makes sense that gene therapy should be restricted to incurable diseases, as this is the only time that taking drastic risks might be warranted. That said, here’s how the U.S. Food and Drug Administration defines gene therapy:17

“Human gene therapy seeks to modify or manipulate the expression of a gene or to alter the biological properties of living cells for therapeutic use. Gene therapy is a technique that modifies a person’s genes to treat or cure disease. Gene therapies can work by several mechanisms:

• Replacing a disease-causing gene with a healthy copy of the gene
• Inactivating a disease-causing gene that is not functioning properly
• Introducing a new or modified gene into the body to help treat a disease”

November 17, 2020, the American Society of Gene + Cell Therapy (ASGCT) announced “COVID-19 Vaccine Candidates Show Gene Therapy Is a Viable Strategy,” noting that:18

“Two COVID-19 vaccine trials, both of which use messenger RNA (or mRNA) technology to teach the body to fight the virus, have reported efficacy over 90 percent.
These findings, announced by Moderna on Nov. 16 and by Pfizer and its partner BioNTech on Nov. 9 … demonstrate that gene therapy is a viable strategy for developing vaccines to combat COVID-19.
Both vaccine candidates use mRNA to program a person’s cells to produce many copies of a fragment of the virus. The fragment then stimulates the immune system to attack if the real virus tries to invade the body.”

mRNA Deliver New Genetic Instructions

As explained in the ASGCT’s video above, mRNA are molecules that contain genetic instructions for making various proteins. mRNA “vaccines” deliver a synthetic version of mRNA into your cells that carry the instruction to produce the SARS-CoV-2 spike protein, the antigen, that then activates your immune system to produce antibodies. Then there’s Moderna’s trial website,19 where they describe their technology thus:

“Typical vaccines for viruses are made from a weakened or inactive virus, but mRNA-1273 is not made from the SARS-CoV-2 virus. It is made from messenger ribonucleic acid (mRNA), a genetic code that tells cells how to make protein, which help the body’s immune system make antibodies to fight the virus.”

November 18, 2020, Wired magazine made a big deal about COVID-19 vaccines being “genetic vaccines,” noting:20

“The active ingredient inside their shot is mRNA — mobile strings of genetic code that contain the blueprints for proteins. Cells use mRNA to get those specs out of hard DNA storage and into their protein-making factories. The mRNA inside Pfizer and BioNTech’s vaccine directs any cells it reaches to run a coronavirus spike-building program.”

Importantly, as reported by David Martin, Ph.D.,21,22 “Moderna … describes its product not as a vaccine, but as ‘gene therapy technology’ in SEC filings. This is because neither Moderna nor Pfizer … make any claims about their products creating immunity or preventing transmission.” Additionally, Moderna’s SEC filings specifically state that “Currently, mRNA is considered a gene therapy product by the FDA,” as well.23

mRNA Is ‘Proven Form of Gene Therapy’
In a February 2021 article, MIT Technology Review reviewed the history of mRNA technology in general, and Moderna’s in particular, stating:24

“Vaccines were not their focus. At the company’s founding in 2010, its leaders imagined they might be able to use RNA to replace the injected proteins that make up most of the biotech pharmacopoeia, essentially producing drugs inside the patient’s own cells from an RNA blueprint. ‘We were asking, could we turn a human into a bioreactor?’ says Noubar Afeyan, the company’s cofounder …”

Bloomberg, in August 2020, reported25 that the Moderna vaccine would seek to transform your body into “a vaccine-making machine.” The New York Times was more to the point. In May 2020, they reported26 that “Researchers at two Harvard-affiliated hospitals are adapting a proven form of gene therapy to develop a coronavirus vaccine.” Read it again — A proven form of gene therapy.
So, to summarize: The definition of “genetic” is something relating to genes, and the definition of “therapy” is the medical treatment of a disease. The definition of “gene therapy” is the process of modifying or manipulating the expression of a gene, or altering the biological properties of living cells.

mRNA are snippets of genetic code that instructs cells to produce proteins. mRNA COVID-19 therapies “deliver genetic instructions into your cells,” thereby triggering your body to produce a fragment of the virus (the spike protein). So, mRNA vaccines ARE gene therapy. There’s simply no way around this. They fulfill all the definitions of gene therapy and none of the definitions for a vaccine.
Defining ‘COVID-19’

There’s yet one more potential problem with the “COVID-19 vaccine” narrative as a whole, which Martin unpacked in a January 25, 2021, interview on the Wise Traditions podcast (above).27 In it, he explains:

“COVID-19 is not a disease. It is a series of clinical symptoms. It is a giant umbrella of things associated with what used to be associated with influenza and with other febrile diseases.
The problem that we have is that in February [2020], the World Health Organization was clear in stating that there should not be a conflation between [SARS-CoV-2 and COVID-19]. One is a virus, in their definition, and one is a set of clinical symptoms. The illusion in February was that SARS-CoV-2 caused COVID-19.
The problem with that definition, and with the expectation, is that the majority of people who test positive using the RT-PCR method for testing, for fragments of what is associated with SARS-CoV-2, are not ill at all. The illusion that the virus causes a disease fell apart. That’s the reason why they invented the term asymptomatic carrier.”

In short, SARS-CoV-2 has yet to be definitively proven to be the actual cause of COVID-19. So, a gene therapy that instructs your body to produce a SARS-CoV-2 antigen — the viral spike protein — cannot even be touted as a preventative against COVID-19, as the two have not been shown to be causally linked.

“They have been willfully lying since the inception of this,” Martin says in the interview. “There is not a causal link between these things … It has never even been close to established.
We have a situation where the illusion of the problem is that people say, ‘I don’t want to get COVID-19.’ What they mean is they don’t want to get infected with a virus. The problem is those two things are not related to each other. A viral infection hasn’t been documented in the majority of what is called cases.
There is no basis for that conflation other than the manipulation of the public. That’s the first half of the problem. The second half of the problem is that what is being touted as a vaccination … is not a vaccine. This is gene therapy …
What is this doing? It’s sending a strand of synthetic RNA into the human being and is invoking within the human being, the creation of the S1 spike protein, which is a pathogen … A vaccine is supposed to trigger immunity. It’s not supposed to trigger you to make a toxin …
It’s not somewhat different. It’s not the same at all … It’s not a prohibiting infection. It’s not a prohibiting transmission device. It’s a means by which your body is conscripted to make the toxin that then, allegedly, your body somehow gets used to dealing with, but unlike a vaccine — which is to trigger the immune response — this is to trigger the creation of the toxin.”

Why the Misrepresentation?
As for why drug companies are misrepresenting this technology, Martin suspects “it’s done exclusively so that they can get themselves under the umbrella of public health laws that exploit vaccination.”

Experimental gene therapies do not have financial liability shielding from the government, but pandemic vaccines do, even in the experimental stage, as long as the emergency use authorization is in effect. This is indeed a major incentive to make sure this technology is perceived as a vaccine and nothing else.
So, by maintaining the illusion that COVID-19 is a state of emergency, when in reality it is not, government leaders are providing cover for these gene therapy companies so that they are insulated from any liability.
Experimental Gene Therapy Is a Bad Idea
I’ve written many articles detailing the potential and expected side effects of these gene therapy “vaccines.” If all of this is new to you, consider reviewing “How COVID-19 Vaccine Can Destroy Your Immune System,” “Seniors Dying After COVID Vaccine Labeled as Natural Causes” and “Side Effects and Data Gaps Raise Questions on COVID Vaccine.”
The take-home message here is that these injections are not vaccines. They do not prevent infection, they do not render you immune and they do not prevent transmission of the disease. Instead, they alter your genetic coding, turning you into a viral protein factory that has no off-switch. What’s happening here is a medical fraud of unprecedented magnitude, and it really needs to be stopped before it’s too late for a majority of people.

If you already got the vaccine and now regret it, you may be able to address your symptoms using the same strategies you’d use to treat actual SARS-CoV-2 infection. I review these strategies at the end of “Why COVID Vaccine Testing Is a Farce.”

Last but not least, if you got the vaccine and are having side effects, please help raise public awareness by reporting it. The Children’s Health Defense is calling on all who have suffered a side effect from a COVID-19 vaccine to do these three things:28

If you live in the U.S., file a report on VAERS
Report the injury on, which is a nongovernmental adverse event tracker (you can file anonymously if you like)
Report the injury on the CHD website


NY Doctor Proved Everyone Wrong About Hydroxychloroquine

Dr. Mercola Interviews the Experts
This article is part of a weekly series in which Dr. Mercola interviews various experts on a variety of health issues. To see more expert interviews, click here.

Many doctors around the world started using the anti-malaria drug hydroxychloroquine (HCQ) early on in the COVID-19 pandemic. Among them is Dr. Vladimir Zelenko, a practicing physician in a Jewish community in Monroe, New York.
He garnered national attention in March 2020 when he told radio host Sean Hannity that he’d had a near-100% success rate treating COVID-19 patients with HCQ, azithromycin and zinc sulfate for five days.1 “I’ve seen remarkable results; it really prevents progression of disease, and patients get better,” he said at the time.
In response, county health officials said Zelenko’s claims were “unsubstantiated” and urged residents to listen to public health officials.2 In this interview, he explains how HCQ works against COVID-19, and discusses the lies spun about the drug to suppress its widespread use. Zelenko had a very active Twitter account and would get millions of views on his tweets, and like many other truth tellers in this crazy pandemic, he was censored and recently removed from Twitter.

“When we have a large population of people that need to be treated, it has to be oral, cheap, safe and effective,” he says. “By the way, this is not new. This information was known in 2005 — even before.
There are papers with [Dr. Anthony] Fauci’s name on it, calling [HCQ] a miracle drug. Fauci called HCQ a vaccine. There’s a paper in which he called it an absolute dream treatment and vaccine. So, it’s conveniently forgotten but that’s what it is. It’s a matter of scientific record.”

What is most impressive to me is that he, through deep research and trial and error in the trenches, determined an incredibly effective protocol, and he did this under enormous personal health challenges. During the spring of last year, he was diagnosed with a type of pulmonary sarcoma that is typically considered terminal, and although improved, he continues to be under treatment for this condition.
Finding Solutions to Avoid a Death Trap

As the SARS-CoV-2 swept through his tight-knit Jewish community, Zelenko was seeing anywhere from 50 to 250 patients per day. At this point, he’s treated more than 3,000 patients with COVID-19-related symptoms. Only one-third of them actually received the triple-drug regimen. The remaining two-thirds were in low-risk categories and did not need drug treatment.
In all, Zelenko has only had 15 patients who ended up requiring hospitalization, four of whom were intubated. All were eventually successfully extubated and recovered. The remaining 11 were admitted for intravenous antibiotics for pneumonia. In all, only three of his high-risk patients died from COVID-19, which puts the mortality rate for this treatment at just 0.3%.

“You cannot ignore that. That’s not even counting the risk stratification patients, which I chose not to treat. In other words, I was able to tell these patients, ‘I know you’re going to be fine. Go home, and you’ll be fine.’ And that has value.
If you include those, the mortality rate is even less. And this has been reproduced. You don’t have to listen to me. You can call it anecdotal all you want, but there are now Harvard professors of virology with 4,000 patient experiences.
Dr. George Fareed, for example, or Dr. Harvey Risch from Yale School of Epidemiology, who has shown that it’s absolutely statistically proven that HCQ used in the prehospital setting is absolutely effective. It’s impossible for it to be a mistake,” he says.

Why HCQ?
Zelenko tells the story of how he got started treating COVID-19 patients with HCQ:

“Hospitals were near capacity and all the outpatient services were closed. Half my staff was sick and all of a sudden I had a war zone. I basically started learning triage medicine, trying to save as many people as possible.
At that time, the whole world had been focusing on building respirators and hospital capacity [instead of putting] emphasis on prehospital care. I found that bizarre because that’s never what we do in medicine. We [use] common sense and intervene in the earliest stages.
It’s much easier to fix a small problem than a large problem. For example, someone has cancer, we don’t wait for it to become metastatic disease. We treat as soon as possible. Someone has a small infection. We put the infection out.
If you look at the CDC, they recommend starting the treatment of influenza with antiviral drugs within the first 48 hours, not the week, except when it came to COVID-19. We were told to send patients home, and when they get sicker, send them to the hospital, where there was a good chance they were going to get intubated, especially in March and April.
At that point, in the city, they had mortality rates above 80%. So, it was a death sentence. None of that made sense to me at all. So, I quickly started to brush up on my virology.
I wanted to understand how this virus works and more importantly, what I can do about it. A series on YouTube called MedCram, Episode 34, saved the world. It explains the biology behind how zinc inhibits RNA polymerase, and the fact that zinc can’t get into the cell. So, it needs help.”

Zelenko goes on to describe how he settled on HCQ, a so-called zinc ionophore, meaning it shuttles zinc into the cell. He decided to treat high-risk patients as early as possible, and this turned out to be key. Early treatment really saves lives when it comes to COVID-19. This is not a situation where the wait-and-see strategy is well-advised.
According to Zelenko, during the first five days of SARS-CoV-2 infection, the viral load remains fairly steady. Around Day 5, it exponentially increases, potentially overwhelming the immune system. This also meant he could not afford to wait for test results, which took about five days. By then, most patients would already have progressed too far.
So, if a patient exhibited symptoms, especially if they reported loss of taste or smell as well, he’d start treatment immediately. In hindsight, about 90% of the tests of people experiencing symptoms had a positive test.
The Synergy of HCQ and Zinc

Zelenko likens HCQ and zinc like a gun and a bullet. HCQ is the gun that shoots the zinc into the cell. Zinc is the silver bullet that kills the virus by inhibiting an enzyme associated with viral replication inside the cell. The antibiotic azithromycin is given to prevent bacterial pneumonia and other secondary bacterial infections that are common in COVID-19.
Today, we have even more information, of course, which means there are more tools available beside HCQ, zinc and antibiotics. Ivermectin, for example, appears very useful, especially for prevention, as do steroids and blood thinners. So, Zelenko will now tweak the treatment of individual patients based on their symptoms.

“It’s not a cookie cutter approach, but what is absolutely the same is that high-risk patients must be treated as soon as possible, within the first five days from onset of symptoms, and they all survive,” he says.

The Psychological Operation Against HCQ
Unfortunately, as discussed by Zelenko, there was essentially a “psychological operation” put into place to scare people away from HCQ. A big part of that was turning it into a political issue. From the start, doctors who used the drug were threatened with the loss of their medical license, which is unheard of for a drug with such a long history of safe use.
The U.S. government made matters worse by only issuing emergency use authorization for in-hospital use and not for outpatient settings. Meanwhile, HCQ has been used for about 60 years in people with chronic conditions such as lupus and rheumatoid arthritis.

“So, the hypocrisy, the loss of common sense, the outright indoctrination killed a lot of people,” Zelenko says. “The root cause of it is the way we educate people. It used to be that higher education was about teaching critical thought and deductive reasoning, analytical analysis.
Now we indoctrinate people into responding to stimuli like dogs, like automatons, like robots. Common sense no longer matters. That’s my critique of higher education and why I think many physicians fell into the trap. Also, this country was traumatized. Even if a doctor was willing to give it, patients were afraid to take it.”

The biggest reason for the fear was unfortunately due to falsified studies and trials using toxic doses. It’s difficult to not suspect an ulterior motive in light of those facts. As noted by Zelenko, a main component of pandemic response, namely prehospital or outpatient treatment, was suppressed.
The question is why? One obvious reason was that it was a presidential election year, and then-president Trump came out in support of HCQ in March 2020. His announcement sparked immediate backlash from a chronically hostile media. “There were plenty of people willing to use every possible way to vilify the president and to discredit anything that might give him a win,” Zelenko says.
Then, of course, there were financial interests at play. Millions of dollars were being invested into new drugs like remdesivir, for example — a drug that costs more than $3,000 per treatment and is only for in-hospital use.
Hospitals were also paid tens of thousands of dollars more for COVID-19 patients, so there was no lack of incentive to get people into the hospital and keep them there either. Meanwhile, Zelenko’s early outpatient treatment costs about $20.
Fraudulent Studies Fueled Distrust

As for the fraudulent and misleading studies, the first to raise alarm was a VA study in Virginia, which found HCQ didn’t prevent death. However, they only used it on late-stage patients who were already on ventilators. From there, they incorrectly extrapolated that it would not be helpful in earlier stages, which simply isn’t true. Other trials simply used the wrong dosage.
While doctors reporting success with the drug are using standard doses around 200 mg to 400 mg per day for either a few days or maybe a couple of weeks, studies such as the Bill & Melinda Gates-funded3 Recovery Trial used 2,400 mg of hydroxychloroquine during the first 24 hours — three to six times higher than the daily dosage recommended4 — followed by 400 mg every 12 hours for nine more days for a cumulative dose of 9,200 mg over 10 days.
Similarly, the Solidarity Trial,5 led by the World Health Organization, used 2,000 mg on the first day, and a cumulative dose of 8,800 mg over 10 days. These doses are simply too high. More is not necessarily better. Too much, and guess what? You might kill the patient. As noted by Zelenko, these doses are “enough to kill an elephant.”
It’s really unclear as to why these studies used such enormous doses, seeing how the dosages this drug is normally prescribed in, for a range of conditions, never go that high. “All those studies did was prove that if you poison someone with lethal doses of a drug, they’re going to die,” Zelenko says.
Then there was the famous Lancet study that the World Health Organization used to justify essentially banning HCQ. This study was withdrawn when it was discovered that the data had been completely and utterly fabricated with falsely generated data from a fly-by-night company. It was supposed to be a meta-analysis of about 90,000 patients, which showed HCQ had lethal effects.
Unfortunately, before it was withdrawn, this fake study resulted in the WHO (or to quote Zelenko, the “world homicide organization”) putting a moratorium on the use of HCQ, which didn’t improve public trust in the drug. Even more egregious, the U.S. Food and Drug Administration used that fake paper as one of its justifications for removing the emergency use authorization for HCQ, even though the study had already been retracted.
Suppression of HCQ Needlessly Killed Tens of Thousands

According to Zelenko, “HCQ is the safest medication in the history of medicine, azithromycin is one of the most common antibiotics used in medicine, and zinc is a mineral that’s well-known and well-tolerated. These drugs were affordable and available to take at home, which was very important. And they worked.”
The virus is not dangerous if you approach it correctly. If you treat it in the right timeframe, it’s no different than a bad flu. You can deal with it. ~ Dr. Vladimir Zelenko
June 30, 2020, Zelenko and two co-authors published a study,6 showing that treating COVID-19 patients who had confirmed positive test results “as early as possible after symptom onset” with zinc, low dose HCQ and azithromycin reduced odds of hospitalization by 84% and all-cause death by 500% compared to no treatment at all.
Crazy enough, even though Zelenko went to great lengths to share his clinical findings with the White House and the National Institutes of Health, he received no support and was told they had no use for it.

“What’s happened over the last 20 years is that the academic elite and pharmaceutical industry have bred a monopoly on medical truth,” he says.
“They feel only data generated through randomized control trials, pharmaceutical sponsored trials, or those that are coming out of major academic institutions are to be viewed as truth. Anything coming from a frontline country doctor must be anecdotal.
That’s the crime here. And they created artificial barriers that prevented the flow of common sense and lifesaving information. You know which countries did take it seriously? See, this is a disease of affluence because the rich countries could afford the waste of money. The poor countries like Honduras … they had no options.
They couldn’t afford respirators. They didn’t have enough hospital capacity. So, they gravitated towards the cheap generic approaches. And those are the ones that have the best outcomes.”

Zelenko highlights Uganda, which has a population of about 50 million people, yet has recorded just 325 deaths.7 “I think this was a genocide against the elderly and a crime against humanity,” he says. “There are plenty of people who have blood on their hands, including the media.”
Coordinated Effort to Cause Harm

He also stresses that the pandemic response, including the suppression of HCQ, has clearly been a global coordinated effort.

“You have to ask yourself, who benefits from a destabilized world? Who benefits from chaos on the streets, from anarchy, from financial despair, from psychological trauma? … In some parts of this country, suicide rates are up 600%.
I speak to my colleagues in emergency rooms — the amount of child abuse and spousal abuse they’ve seen is absolutely ridiculous. The amount of collateral damage from preventable illnesses, like heart disease and cancer that are skyrocketing because people are not getting access to routine care.
A lot of people weren’t getting elective surgeries on time. So, there’s been a lot of collateral damage. The shutdown is killing more people than the virus. The virus is not dangerous if you approach it correctly. If you treat it in the right timeframe, it’s no different than a bad flu. You can deal with it. You don’t have to shut down the world.”

The True Agenda Coming Into Plain Sight

Indeed, the world is becoming increasingly black and white and it’s becoming easier and easier to see that global and national systems are not benefiting but, rather, enslaving the population, and how they’re doing it. As noted by Zelenko:

“I see the world now with such clarity … It’s no longer confusing. It’s a binary choice. It’s very clear who’s on what side. And here are the teams: There are those who want to live a life of God, conscious … Our lives have sanctity. They’re priceless and they should be preserved at all costs. And no one has the right to enslave another human being. That’s one approach.
The other is [internment] … an attempt to enslave, psychologically, and even more so physically, the world population. Do you want to know what’s coming? Look at Justin Trudeau statements. Justin Trudeau, the prime minister of Canada, just announced that anyone who tests positive will be quarantined in a government-run facility, until the government deems you safe to return back to society.
That’s [also] what Cuomo wants to do in New York. And I’ll tell you what I think. For what I’m about to say, I’m going to be labeled as a conspiracy theorist. But you know what? I don’t care because, eventually, the truth will come out and history will prove it right.
If you look at the United Nations and the World Economic Forum, they have a plan. They have a 30-year plan, they have 100-year plan. That’s all spelled out in their charter. Just look at it.
So there’s a plan called the 2030 plan. You can go to the World Economic Forum and look at their own words. It’s being run by Klaus Schwab and his group. He wrote a book called ‘The Great Reset.’ That’s where the term comes from.
Now, all the governments are quoting him, like Justin Trudeau, Prince Charles, the Australian prime minister. There’s a myriad of other politicians calling for the great reset. So, what is the great reset? What are they asking for?
No. 1, I mean it’s absolutely ridiculous, but they’re saying, ‘You will own nothing and you will be happy.’ That is their mission. No. 2, America will no longer be a superpower. No. 3, there will be a small group of nations that determine the direction of where the world goes. No. 4, you won’t eat meat except as an occasional treat.
No. 5, there’ll be a global tax on fossil fuels to eradicate the reliance on oil. No. 6, a billion refugees will be displaced [and] we’re going to have to incorporate them and absorb them into our society. These are their stated goals.
Now, how do you take the world’s biggest country, most powerful country, richest country and make it no longer a world superpower? Well, that’s exactly what they’re doing. The economy is in shambles.
You’ve put in a government now that is passing foreign relief aid to China, Russia, Syria, Iran, the Palestinian Authority. They’re sending billions of dollars now to financially support these countries. So, you have to ask yourself, what is going on here?

This all started many years ago, but when Trump went to Davos, in the first few years of his presidency, he said, ‘I’m not part of your globalist agenda. I’m going to put my national interest first.’ That was a poke in the eye of the globalists. That’s the point when George Soros came out and said that Trump is one of the most dangerous people on the planet and he needs to be brought down.
He was dangerous to their agenda. So, what we’re really fighting for is the soul of man. God is testing us, in my opinion. Every person is being asked one simple question, either bow down to God and have the divine presence protect you or you’re going to bow down to Bill Gates … I’m calling for Nuremberg 2.0. These people need to be brought to justice.”

There’s No Rational Justification for COVID-19 Vaccines

Zelenko also shares his views on the COVID-19 mRNA vaccines. He points out that while Gates is pushing COVID-19 vaccines, ostensibly to save lives, he’s on record saying he feels the world population needs to be reduced.

“If someone was a eugenicist and feels that the world population needs to be reduced, why would I take his vaccine for my health?” he asks. “The logical inconsistencies here are absolutely perverse.
I’m so pro-vaccine you can’t imagine. I’ve given tens of thousands of patients vaccinations. I give it to myself and to my children. However, I’m not COVID-19 vaccine positive. And I’ll tell you why: Because the majority of patients under the age of 45 have a near-100% recovery rate with a mild, runny nose from COVID-19. Why would I vaccinate someone with an experimental vaccine? The answer is not for medical reasons.
Another question, why would I give someone a vaccine, even if they are at high risk, if I can give them prophylaxis and/or early prehospital treatment and have a 100% recovery rate? Not for medical reasons.
Another question: Why would I give a vaccine to someone who’s already had COVID-19 and has antibodies? Not for medical reasons. And why would I give a very specific vaccine to someone who is going to be exposed to a ton of different variants and strains and mutations?
I wouldn’t. What I would use is an approach that inhibits RNA replication of RNA viruses, which works for all the strains, including, potentially, influenza. That’s the big dirty secret here.”

It’s Safe to Stop Living in Fear
Zelenko, who was born in a communist country and whose family suffered under communist and fascist rule, is quite sensitive to the signs of these authoritarian regimes. He recounts a story told in the book “The Gulag Archipelago” by Alexander Solzhenitsyn.
Stalin wanted to dig a canal from Moscow to St. Petersburg. The work, done in the middle of winter, led to the death of 400,000 prison workers, as they weren’t given the appropriate clothes or tools. The bodies were thrown into the cement and became a permanent part of the canal.

“No ship ever used the canal because it was too shallow. So, the question was, why was this canal built? And the answer is: So that 400,000 people would die,” Zelenko says.
“I’m not attacking the vaccine. I’m attacking the need for the vaccine. I have not enough information to say it’s good or bad. And I don’t like to guess. But what I can tell you is that I know for a fact that 99.98% of young and healthy people under the age of 45 recover, with no treatment.
I also know for a fact, from my own real-world battle-tested evidence, which has been reproduced now on hundreds of thousands of patients, that if you intervene early, you essentially eliminate hospitalization and death. And, I’ve now treated two waves. I have not seen one patient who’s had COVID-19 in the first wave, get it again …
So, the need for the vaccine doesn’t exist. It’s … been artificially conflated … offering people an artificial false hope solution in order to enslave them to be codependent on government. You know why my approach is so dangerous? Because not only does it treat COVID-19, [but] it treats anxiety. It tells people you don’t need to worry.
My statement to the American people or whoever’s listening is: Return to normal living. You do not need to worry. And by the way, there are nonprescription options … that can replace HCQ if your government or doctor are too stupid or vicious to give it to you. So, you don’t have to rely on them. You can buy over-the-counter things that will save your own life. So, my point is, return back to normal life …
It’s unbelievable the crime that’s been done on the human psyche. I’m screaming to humanity: Don’t be scared! Be cautious. Be smart. Use common sense. But don’t be scared. Return back to life. Reengage in life.”

HCQ Mechanisms of Action and Alternatives

Over-the-counter alternatives to HCQ include EGCG (green tea extract) and quercetin, both of which are zinc ionophores and therefore work much like HCQ does. Quercetin works best when taken in conjunction with vitamin C, however, as the vitamin C helps activate it. Zelenko recommends taking 1,000 milligrams of vitamin C with it.
Now, HCQ does have other mechanisms of action beside being a zinc ionophore, so it’s a better choice, but if you simply cannot get it, EGCG or quercetin are viable stand-ins. Additional benefits of HCQ include:

Inhibiting viral entry into the cytoplasm, in part by changing the pH
Inhibiting cytokine storms through anti-inflammatory properties
Stabilizing red blood cells, which improves oxygenation

“Since it has four different mechanisms of action, it’s a very effective drug, and it has a half-life of 50 days in plasma,” Zelenko says. “But if you can’t get it, you can’t get it. So, I’ll take quercetin or EGCG.”
The caveat here is you must implement this treatment within the right timeframe. It can be helpful to recognize we are in essence dealing with two diseases, or stages of disease, here.
First, there’s the viral infection, and second, there’s the immune over-response that leads to the release of inflammatory cytokines and agents that can cause blood clots. The key is to prevent the progression from the first stage to the second.
Prescription Help Is Available

Like many others who have dared run the gauntlet that is HCQ promotion, Zelenko has been attacked from several angles. His character has been assassinated in the press, his medical credentials questioned and threatened, and his online presence silenced. 

“I had had zero media experience before March 2020. I am of a quiet doctor who was taking care of his patients, living a serene life. All of a sudden, this all exploded on me …
I was on Twitter, getting 10 million impressions per tweet. They shut me down last month for platform manipulation. I’m not even sure what that means. So, I had to develop my own website. It’s free and has my protocols in 20 different languages.”

To learn more about Zelenko’s protocol, be sure to visit his website, There, you’ll find protocols not only for early treatment but also prophylaxis, along with studies that document the rationale for each of the treatment components and patient testimonials.
His website also includes access to telemedicine via “Speak With an MD,” which can overnight your medication. “So, if you live in a state that’s tyrannical, you can have a consultation with Dr. Fields,” Zelenko says. “I had to develop this because there were patients around the country who didn’t have access [to HCQ].”
HCQ should be available to most people in the U.S. at this point, but you do need a prescription, and some doctors are still unwilling or resistant to prescribe it. Other times, pharmacies can create roadblocks. “It may take some diligence but none of my patients goes without the medication written for them,” he says.
Early Treatment Prevents ‘Long Haul’ Side Effects

In closing, it’s worth noting that when you treat early, your risk of developing long-term side effects, commonly referred to as “long-haulers,” is virtually nil. Not a single one of Zelenko’s patients who received treatment within the first five days of symptom onset went on to develop long-haul symptoms afterward.

“I had patients that were long-haulers, but they came to me after that window, and they were already advanced in the inflammatory process. At that point, the cytokine storm had already taken hold. They had developed blood clots, some of them had pulmonary infarct, or strokes actually.
Others developed ARDS or catastrophic lung damage and pneumonias, and others just are not themselves. I don’t know how to describe it, but it ate away part of their souls. They’re not the same people. There’s depression, there’s lack of energy. There’s a psychological impact as well.
So, it’s not that I don’t deal with long-haulers, I do. But the way to prevent the long-hauler syndrome is to intervene within the first five days, with appropriate antiviral medication in high-risk patients. That is 100% successful,” he says.

The Light of Truth Will Prevail
Zelenko refers to the COVID-19 pandemic and everything surrounding it as an information war, a propaganda war, and his primary objective and agenda in this war is to educate and speak truth.

“There’s a lot of false narrative being pumped into the heads of people, to create fear,” he says. “In the Psalms of David, it says, ‘With crooked people, you have to deal crookedly.’ It also says you should learn from a thief.
So, I learned from the enemy, and I use their tactics to counter them. The main tactic is to spread truth. By the way, it’s no longer dependent on me. I have second and third and fourth generation leaders that have taken on the mission and are really spreading the knowledge worldwide.
It’s unstoppable. They could try to slow it down, and they are. But the truth will come out. The truth is coming out. And when the truth will be revealed, the people that try to obstruct it and use lies to slaughter, will be destroyed by it, God willing.
I am now more optimistic than I’ve ever been, simply because there’s no more confusion. Life was very confusing. You didn’t know what was good, what was bad. Now, it’s very clear. There’s much more bad, that’s true. But I know where it is. I know where the enemy is. And I know where the good is. And a little light pushes away a lot of darkness.”


COVID-19 Vaccine Tested on Babies and Pregnant Women

Pharmaceutical and medical device giant Johnson & Johnson, Inc. (J&J) announced on February 28, 2021, plans to test its experimental Ad26.COV2.S vaccine for COVID-19 on infant children (including newborns), pregnant women and people with compromised immune systems.

J&J did not include infants, pregnant women or the immunocompromised in the U.S. population in clinical trials on the experimental COVID-19 vaccine last year.1,2,3 A recent article in New York Magazine noted:4

“The initial clinical trials for COVID-19 vaccines didn’t include children, which is standard practice; now, trials for younger children are happening in descending order of age, calibrating the best dosage for each cohort.”

The announcement by J&J came the day after the U.S. Food and Drug Administration (FDA) granted J&J subsidiary Janssen Biotech Inc. an emergency use authorization (EUA) to distribute the vaccine in the U.S. for use by individuals 18 years of age and older. Currently, the single-dose Ad26.COV2.S vaccine cannot be given to anyone in the U.S. under 18 years old.5,6,7,8,9

According to a spokesperson for Janssen, which manufactures Ad26.COV2.S, the single-dose vaccine will first be tested on children between 12 and 18 years old. Afterward, J&J will proceed quickly to test the vaccine on infants, pregnant women and immunocompromised people.10

FDA Reviewed J&J Plans to Test COVID-19 Vaccine on Babies

J&J’s move to test its COVID-19 vaccine on very young children, as well as pregnant woman and immunocompromised people, was expected. The plans to perform these clinical trials were reportedly included in J&J’s application to the FDA for EUA and were discussed by members of the FDA advisory committee that reviewed J&J’s data on Ad26.COV2.S.11,12

“They (J&J) did not get into a lot of detail about it but did make it clear they will be pursuing pediatric and maternal coronavirus immunization studies,” said FDA advisory committee member Dr. Ofer Levy, Ph.D., director of the Precision Vaccines Program at Harvard University’s Boston Children’s Hospital.13

Other Companies Testing COVID-19 Vaccines on Older Children

J&J’s planned COVID-19 vaccine clinical trials will be the first to include infants. AstraZeneca plc, which has produced the experimental AZD1222 vaccine for COVID-19 in partnership with Oxford University, has been conducting clinical trials on children as young as 6 years of age, while Moderna Inc. and Pfizer Inc. (in partnership with BioNTech SE) are currently testing their experimental mRNA-1273 and BNT162b2 COVID-19 vaccines on children as young as 12.14,15

J&J began shipping out 4 million doses of Ad26.COV2.S on March 1, 2021. The company has pledged that it will have 20 million doses of the vaccine ready to distribute by the end of March and 100 million doses by this summer.16


Weekly Health Quiz: Vaccines, Bill Gates and AGRA

1 If you are injured by a COVID-19 vaccine in the U.S., you may be able to obtain compensation through which of the following?
The National Vaccine Injury Compensation Program (NVICP)
The Vaccine Adverse Event Reporting System (VAERS)
The Countermeasures Injury Compensation Program (CICP)
In the U.S., vaccine makers already enjoy full indemnity against injuries occurring from the COVID-19 vaccine under the PREP Act. If you’re injured, you’d have to file a compensation claim with the Countermeasures Injury Compensation Program (CICP), which is funded by U.S. taxpayers. Learn more.
Civil lawsuit against the vaccine manufacturer

2 What is Operation Mockingbird?
A covert program by the British Foreign and Commonwealth Office to weaken Russia’s influence with propaganda published by Reuters and BBC News
A surgical procedure to correct a rare speech impediment
A smart TV-based surveillance program run by the NSA
A clandestine CIA media infiltration campaign in which journalists are paid to publish fake news
Operation Mockingbird was a clandestine CIA media infiltration campaign launched in 1948. However, infiltration and manipulation of the media has been a routine occurrence since 1915, when J.P. Morgan interests purchased editorial control of 25 of the most influential newspapers, thereby allowing them to control news that were crucial to their private and corporate interests. Learn more.

3 To minimize the death toll from COVID-19, which of the following strategies is likely to be the most effective?
Educate and encourage implementation of a “clean” whole food diet and healthy lifestyle by all
If we really want to protect the masses, we need to educate and promote healthy living at all stages of life. Improving your health through a healthy lifestyle, sunshine, fresh air and real food, is the best way to protect the most people against viral infections such as COVID-19. Learn more.
Quarantine all living beings for two years
Vaccinate every person on earth
Encourage infection transmission to speed herd immunity

4 Bill Gates-funded AGRA has for the past 14 years been working to improve hunger in Africa. In that time:
Hunger has been reduced by half
Hunger has increased by 30%
In 2006, Gates launched AGRA together with the Rockefeller Foundation. After 14 years, AGRA’s influence has significantly worsened the situation in the 18 African nations targeted by this “philanthropic” endeavor. Hunger under AGRA’s direction increased by 30% and rural poverty rose dramatically. Learn more.
Hunger has remained the same
Hunger has been reduced by 75%

5 What was the previous name of the Galton Institute?
The Wellcome Trust
The U.K. Eugenics Society
The Galton Institute was formerly known as the British Eugenics Society. AstraZeneca’s COVID-19 vaccine was co-developed by Adrian Hill, who has long-term ties to the British eugenics movement through his affiliation with the Galton Institute. Learn more.
The Centre for Human Genetics

6 Which of the following is the most effective way to optimize your energy and combat fatigue?
Daily aerobic exercise such as long-distance running
Severe calorie restriction (about 30% of normal calorie intake)
Walking barefoot as often as possible
Time-restricted eating (eating all meals within four to six hours each day)
One of the most effective ways to optimize your energy and combat fatigue is to implement time-restricted eating (TRE), as it improves your mitochondrial health and metabolic flexibility. Learn more.


These Herbs Might Help You Fight Respiratory Viruses

Over thousands of years, indigenous cultures have used traditional herbal medicine to prevent and treat diseases, including respiratory ailments like colds and influenza. In the modern day, the bioactive compounds of medicinal plants have become primary points of research for drug therapies, but the plant remedies still hold promise when used as nature intended.

“While the plant kingdom continues to serve as an important source for chemical entities supporting drug discovery, the rich traditions of herbal medicine developed by trial and error on human subjects over thousands of years contain invaluable biomedical information just waiting to be uncovered using modern scientific approaches,” researchers wrote in Nature Plants in 2017.1

Now, with the COVID-19 pandemic, the use of traditional herbal medicine for the treatment of respiratory ailments has taken on renewed interest, and researchers from the Chinese Academy of Agricultural Sciences and China’s Hebei Agricultural University compiled some of the most useful herbs for the prevention and treatment of cold and flu, and potentially COVID-19, too.2

Top Expectorant Herbs for Cold and Flu

Expectorant herbs are useful for thinning and loosening mucus, helping to clear congestion. They’re often used for coughs and colds, as they may make breathing easier.

After conducting a literature survey on natural herbal medicines, particularly those from traditional Chinese and Persian medicine, the researchers suggested the following herbs had significant potential as expectorants for cold and flu:3

Tulsi — Tulsi, also known as holy basil, is an Ayurvedic herb with antibacterial, antiviral, antifungal, anti-inflammatory, analgestic, antioxidant and adaptogenic properties.4 A review in the Journal of Ayurveda and Integrative Medicine even called tulsi an “herb for all reasons,” noting that it’s effective against “a range of human and animal pathogens” with broad-spectrum antimicrobial activity. They even suggested it could be used as a hand sanitizer.5

Tulsi is also one of the herbs in Ayush Kwath, an Ayurvedic herbal formula recommended by the government of India to boost immunity and combat COVID-19.
“Ayush Kwath due to its immune-modulatory, antiviral, antioxidant, anti-inflammatory, anti-platelet, anti-atherosclerotic, hepato-protective, reno-protective properties; seems to be effective in immuno-regulation for controlling viral infections like COVID-19,” a team of researchers wrote in the Journal of Ayurveda and Integrative Medicine.6

Snake root — Used by North American Indians to treat snake bites, snake root, or Polygala senega, is also valued for its stimulant, expectorant properties and has traditionally been used to treat respiratory ailments.7

Licorice root — Licorice root contains liquiritin, a compound that helps prevent the rapid reproduction of SARS-CoV-2, the virus that causes COVID-19, as demonstrated in the lab.8 The compounds in licorice root have demonstrated antiviral and anti-inflammatory effects in the body and the ability to modulate the immune system.

A second compound in licorice root that has demonstrated an effect against SARS-CoV-1 is glycyrrhizin.9

Glycyrrhizin has traditionally been used in the treatment of coughs and viral respiratory tract infections in China, India and Greece, and animal studies suggest it reduces mortality from herpes encephalitis and influenza A pneumonia, while in vitro studies show it has “antiviral activity against HIV-1, SARS-related coronavirus, respiratory syncytial virus, arboviruses, vaccinia virus and vesicular stomatitis virus.”10

Clove — Cloves (Syzygium aromaticum or Eugenia cariophylata) are the aromatic flower buds collected from evergreen trees of the same name. Eugenol, a major volatile constituent of clove essential oil, has a range of pharmacological activities including antimicrobial, anti-inflammatory, analgesic, antioxidant and anticancer properties.11
One way to use clove as a respiratory aid is to make clove tea, which you can either drink or use as a steam inhalation. For a cold, you can add a couple of drops of clove essential oil to a mug of hot water, sweetened with raw honey or stevia if desired. Drink two to three glasses a day until your condition improves. You can also use clove oil for aromatherapy by diffusing it into the air.

Slippery elm root — The inner bark of the slippery elm tree is a slimy substance that, when mixed with water, creates mucilage, a sticky substance traditionally used for soothing a variety of ailments. In addition to being used for gastrointestinal problems like irritable bowel syndrome,12 slippery elm is beneficial for the throat and coughs, and has soothing effects on the tissue of the upper airway.13

Marshmallow root — This perennial herb has been valued for treating respiratory ailments since ancient times, and research suggests that, when added to an herbal cough syrup, it’s useful for alleviating cough associated with colds, bronchitis and respiratory tract diseases that involve the formation of mucus.14

Sage — Sage, in addition to having antimicrobial and anti-inflammatory properties, is a natural expectorant and useful to clear mucus and reduce coughs, and even calm a sore throat.15 Consider adding a drop of sage essential oil to a cup of tea or hot water the next time you have a cold.

Top Antiviral and Immunostimulant Herbs

In their review of the best herbal medicines for cold and flu, in addition to COVID-19, the researchers of the featured study also highlighted antiviral herbs and those that stimulate the immune system. While most medicinal plants have a variety of benefits with overlapping therapeutic properties, the following stood out in these categories. Important antiviral herbs included:

Thyme — Thyme (Thymus vulgaris), contains potent compounds like thymol, camphene, linalool, and carvacrol and has been used traditionally for respiratory issues. Modern research shows vaporized essential oils from thyme, among others, may “potentially useful in influenza therapy.”16
Venezuelan officials also announced they have had encouraging results treating COVID-19 patients with Carvativir, an oral solution made from extracts of thyme and oregano.17

Honeysuckle flowers — Honeysuckle (Lonicera japonica) is another plant with a long history of use for respiratory ailments.18 It contains chlorogenic acid, which one study found “inhibited influenza virus during the late stage of infectious cycle” and also effectively reduced inflammation in the lungs and reduced viral titers during the study.19

Andrographis — This adaptogenic and antiviral herb has been used in Traditional Chinese Medicine and Ayurveda to treat the common cold.20 In a systematic review of 33 randomized controlled trials with 7,175 patients, andrographis helped relieve the symptoms of acute upper respiratory tract infection and shortened the time for cough and sore throat as well.21
In another review of the literature, scholars found “strong evidence” that Andrographis was superior to a placebo in reducing the frequency and severity of coughs.22 A formulation known as Kan Jang that combines andrographis and Siberian ginseng has also been studied, with positive results, in the treatment of colds,23 upper respiratory tract infections,24 sinusitis25 and flu.26

Yarrow — This perennial herb contains many constituents with pharmacological activity. It’s traditionally been used for respiratory infections, colds and flu,27 and is sometimes combined with elder flower for this purpose.

Peppermint — Peppermint oil acts as an expectorant and decongestant, and may help clear your respiratory tract. Use peppermint essential oil as a cold rub on your chest or inhale it through a vaporizer to help clear nasal congestion and relieve cough and cold symptoms.
For even more therapeutic punch, try a tea made from a combination of elderflower, yarrow, boneset, linden, peppermint and ginger.

Calendula — Also known as marigolds, calendula has anti-inflammatory, antiviral and regenerative properties that are also stimulating for the immune system.28

The following herbs, in addition to marshmallow root and slippery elm, were also highlighted for their immunostimulant properties particularly for cold and flu:

Echinacea — In a study published in Integrative Cancer Therapies, echinacea was found to reduce the severity and duration of colds if it is administered right away once symptoms appear.29

Garlic — With both immune-boosting and antiviral effects, those who consumed garlic daily for three months had fewer colds than those who took a placebo.30

Ginseng — Another adaptogenic herb, older adults who took an extract of American ginseng had a 48% reduction in relative risk, and a 55% reduction in duration, of respiratory illness.31 This herb was also found to be “a safe and effective treatment for reducing the absolute risk of recurrent colds and the mean number of colds per person.”32

Isatis root — Isatis is a flowering plant used in TCM and Ayurveda, often in combination with other herbs. Teas and mouthwashes containing isatis, honeysuckle, mint and licorice root have also been successful at treating respiratory problems, including influenza.33

Usnea lichen — Usnea is a type of lichen that grows on trees and rocks around the world. It contains polysaccharides that may boost immune system activity, making it useful for colds and flu.34

Myrrh — Myrrh is a thorny tree or shrub that releases a resin from cracks in the bark. This resin has traditionally been used to treat colds and cough,35 and with known antiviral and immunomodulatory properties, researchers suggested myrrh mouthwash could be effective in combating COVID-19.36

Ginger — Ginger root has been used as a tonic to treat common ailments for centuries, and a number of studies have documented the antioxidant and immunomodulatory effects of this herbaceous perennial plant.37

Nature Is Full of Powerful Healers

Herbal medicine is a powerful arsenal in the prevention and treatment of respiratory ailments like colds, flu and COVID-19. In China, herbal treatment is recommended for children and adults with COVID-19,38 and interest in traditional remedies is growing in the U.S. as well.
Herbs are unique in that they contain multiple beneficial components that work synergistically to promote wellness. As noted in the featured study:39

“Some important chemical constituents of traditional herbs, which can be considered in the fight against COVID-19, are betulinic acid, coumaroyltyramine, cryptotanshinone, desmethoxyreserpine, dihomo-?-linolenic acid, dihydrotanshinone I, kaempferol, lignan, moupinamide, N-cis-feruloyltyramine, quercetin, sugiol, and tanshinoneIIa.”

Because working with herbs can be complex, for best results consult with a knowledgeable natural health care practitioner who can guide you on the appropriate herbal solutions for your circumstances.


FDA Warns Dr. Mercola to Stop Writing About Vitamin D

In the summer of 2020, the Center for Science in the Public Interest (CSPI) — a consumer advocacy group partnered with Bill Gates’ agrichemical PR group, the Cornell Alliance for Science,1 and bankrolled by billionaires with ties to Monsanto, the Gates Foundation, the Rockefeller Foundation, the Rockefeller Family Fund and Bloomberg Philanthropies2 — launched a social media campaign to put an end to
July 21, 2020, CSPI issued a press release3 in which they accused me of falsely claiming “that at least 22 vitamins, supplements and other products available for sale on his web site can prevent, treat, or cure COVID-19 infection.” This despite the fact that their Appendix of Illegal Claims4 clearly show no COVID-19-related claims exist on any of the product links.
The group also testified in a Senate hearing on the topic of COVID-19 scams and urged the U.S. Food and Drug Administration and the Federal Trade Commission to take regulatory action against me.
In an August 12, 2020, email, CSPI president Dr. Peter Lurie5 — a former FDA associate commissioner6 — made the spurious claim that I “profit from the COVID-19 pandemic” through “anti-vaccine fearmongering” and reporting of science-based nutrition shown to impact your disease risk.
Former FDA Official Pulls Strings to Target Natural Health
Seeing how Lurie is a former FDA official, it’s disheartening, but not surprising, that the FDA has now issued us a warning letter7 for “Unapproved and misbranded products related to COVID-19.” Lurie has publicly taken credit for the FDA’s action,8 thereby establishing the potential that CSPI is pulling strings under the new administration through relationships they did not have back in August when they first launched their assault on my free speech.
According to the FDA, vitamin C, vitamin D3 and quercetin products are “unapproved new drugs sold in violation of section 505(a) of the Federal Food, Drug, and Cosmetic Act.” The agency is also listing on its Fraudulent COVID-19 Products page.
Lurie seems to be hinting that he also wants federal authorities to remove my StopCOVIDCold site, where you can download a free scientific report detailing the benefits of maintaining appropriate vitamin D levels to protect against viral infections. He’s also urging “state attorneys general to investigate how they may further protect consumers from Mercola’s illegal marketing.”9

“Americans are justifiably concerned about becoming infected with the coronavirus and contracting COVID-19. Being misled to believe that supplements could prevent or treat COVID-19 could cause consumers to fail to take protective measures such as mask-wearing, putting themselves and others at risk, or fail to seek actual medical treatment if sick,” Lurie writes.10

It’s ironic that Lurie dismisses offhand peer-reviewed published science demonstrating certain nutrients can boost your immune function and help lower your risk of severe infection — be it from SARS-CoV-2, the seasonal flu or anything else — and touts mask wearing, which has no published scientific evidence to back its universal use, as one of the most important prevention strategies against COVID-19.
Sadly, this is where we are nowadays. “Trust the science,” they say, while simultaneously promoting scientifically unverified claims and trying to eradicate anyone who simply reports the findings that are actually published in the medical literature that may negatively impact the pharmaceutical industry.
CSPI and FDA Cannot Censor Speech

The CSPI is trying to censor my efforts to educate people on how to avoid vitamin D deficiency which, without doubt, places them at far higher risk of complications and death from respiratory infections. Well, I am not going to allow people to die from COVID-19 and other respiratory infections due to vitamin D deficiency.
In October 2020, I co-wrote a paper together with William Grant, Ph.D.,11 and Dr. Carol Wagner,12 both of whom are on the GrassrootsHealth vitamin D expert panel, demonstrating the clear link between vitamin D deficiency and severe cases of COVID-19. This paper was published in the peer-reviewed medical journal Nutrients.13
With that, I have established my medical and scientific merit, and will continue to express my professional opinions, based on the available science, and defend my freedom of speech as the U.S. Constitution provides for.
The FDA’s warning letter highlights statements in articles on my website that are fully referenced and supported by published science. I am committed to providing truthful information, for free, to anyone that wants it, and I’m all for having a rigorous scientific debate when necessary. CSPI has taken credit for pressuring the FDA to issue this warning letter to suppress free speech. The FDA’s warning letter is simply another attempt by CSPI to smear me with false accusations.
If scientists and researchers are publishing these studies, how can it be a crime to report their findings? At the end of the day, the CSPI’s attacks on this website amounts to an effort to suppress science itself.
As CSPI well knows, thanks to the U.S. constitution and the first amendment, I have every right to speak publicly on matters regarding health, so this is nothing but another attempt to “cancel” me while concealing its own duplicity. For the record, we have fully addressed the warning letter; the FDA cannot simply stop free speech that CSPI does not like.
This Is NOT the First Time CSPI Has Endangered Public Health

CSPI continues to be a vitamin D denier even though overwhelming evidence points to its ability to reduce the risk of developing severe COVID-19. This isn’t surprising, coming from a Rockefeller-funded organization that pushed deadly trans fats on the American public until the facts became undeniable, at which point they simply rewrote the organization’s history on this subject to hide its past stance.
In 1986, CSPI described trans fat as “a great boon to Americans’ arteries.”14 Two years later, in 1988, they still praised trans fats,15 saying “there is little good evidence that trans fats cause any more harm than other fats” and that “much of the anxiety over trans fats stems from their reputation as ‘unnatural.'” Meanwhile, in the real world, the CSPI’s highly successful trans fat campaign resulted in an epidemic of heart disease.
The CSPI’s role in the promotion of trans fats and its influence on the food industry was discussed in David Schleifer’s article, “The Perfect Solution: How Trans Fats Became the Healthy Replacement for Saturated Fats,”16 in which he noted that:

“Scholars routinely argue that corporations control US food production, with negative consequences for health … However, the transition from saturated to trans fats shows how activists can be part of spurring corporations to change.”

It wasn’t until the 1990s that CSPI started reversing its position on synthetic trans fats, but the damage had already been done, and it never admitted its error. In fact, rather than openly admitting it had misled the public with erroneous claims, CSPI simply deleted sections of its previous support of trans fat from the web.17 Notice how their historical timeline18 of trans fat starts at 1993 — the year CSPI realized the jig was up and they had to support the elimination of trans fat.CSPI then started raising money for campaigns to stop the heart disease causing substance they first promoted. How diabolical is that? Create the problem and then take money from others for the solution. 

>>>>> Click Here <<<<< This obfuscation was noted by Mary Enig, Ph.D., in a 2003 article, in which she wrote:19 “On October 20, 1993, CSPI had the chutzpah to call a press conference in Washington, DC and lambast the major fast-food chains for doing what CSPI coerced them into doing, namely, using partially hydrogenated vegetable oils in their deep fat-fryers. On that date, CSPI, an eager proponent of partially hydrogenated oils for many years, even when their adverse health effects were apparent, reversed its position after an onslaught of adverse medical reports linking trans fatty acids in these processed oils to coronary heart disease and cancer … Thanks to CSPI, healthy traditional fats have almost completely disappeared from the food supply, replaced by manufactured trans fats known to cause many diseases. By 1990, most fast food chains had switched to partially hydrogenated vegetable oil … Who benefits? Soy, or course … [and] in CSPI’s January, 1991 newsletter, Jacobson notes that ‘our effort was ultimately joined … by the American Soybean Association.’” Even more egregious is the CSPI’s continued recommendation to eat unsaturated fats like soy and canola oils20 and avoid butter and other healthy saturated fats, saying that “changing fats doesn’t lower the risk of dying.”21 This wholly disregards the compelling evidence showing that industrial vegetable oils, omega-6 linoleic acid in particular, pose significant health risks and contribute to chronic disease. And chronic disease, in turn, impacts mortality.  CSPI Primarily Protects Big Business This tendency to fall in line with industry science and propaganda has become a trend within CSPI. For example, it wasn’t until 2013 that CSPI finally downgraded the artificial sweetener Splenda from its former “safe” category to one of “caution.”22 In 2016, they downgraded it again, from “caution” to “avoid.”23 Despite that, CSPI continues to promote diet soda as a safer alternative to regular soda, saying it “does not promote diabetes, weight gain or heart disease in the way that full-calorie sodas do.”24 The group has also taken a strong pro-GMO stand and actively undermined the GMO labeling movement,25 which resulted in the U.S. being the only country in the world that does not have clear GMO labeling. In August 2001, the organization actually urged the FDA to take enforcement action against food companies using non-GMO labels, claiming such labels could “deceive consumers.”26 In a similar vein, the group opposes clear labeling of ultraprocessed fake meat. In a May 2018 letter to the FDA,27 CSPI urged the agency “to reject efforts by the United States Cattlemen’s Association to prohibit use of the terms ‘meat’ or ‘beef’ on plant-based and cultured proteins marketed as alternatives to traditional meat.” All in all, it appears the CSPI is completely against the idea of a well-informed public. The CSPI has also been a promoter of the thoroughly debunked low-fat myth. In 1995, they launched a “1% or Less” campaign that urged everyone over the age of 2 to switch from whole and 2% milk to skim milk (also known as nonfat or fat-free milk) in order to reduce their saturated fat intake.28,29,30  It was another successful campaign that resulted in the doubling of skim milk sales.31 However, just like their trans fat campaign, this was equally ill advised, seeing how research32,33 shows full-fat dairy actually lowers your risk of death from diabetes and cardiovascular causes such as stroke. CSPI Has Repeatedly Violated Its Mission Statement  Considering the suspected, and in some cases well-verified, health hazards of trans fats, artificial sweeteners, soy, GMOs, low-fat diet and fake meat, CSPI’s intent to protect and advance public health is questionable to say the least. It seems they’re more interested in protecting profitable industries, and the CSPI’s efforts to destroy companies selling vitamins and supplements with natural antiviral effects34 is simply more evidence of that. The fact is, they’re seeking to bring an end to because we are such a serious threat to their agenda and they want to eliminate as many of the truth tellers as they can.