Editor’s Note: You can be damn sure that if the FDA goes through with their nefarious scheme that those in Canada who also rely on homeopathic medicines will also be directly affected. We know WHO controls the FDA so this is must one more direct attack up the people that must be stopped.
U.S. Food & Drug Administration Declares Homeopathy Illegal
The homeopathic drugs you rely on have been declared illegal by the FDA, meaning the agency can wipe them off the market whenever they wish. We must fight back. Action Alert!
This is the beginning of the end for homeopathy unless we do something about it. The FDA has completed their overhaul of homeopathy regulation, and it is as we feared: in the FDA’s view, all homeopathic products are illegal. This interpretation gives the agency the power to remove any homeopathic medicine it wants to, whenever it wants to. We must convey consumer outrage to Congress and the FDA if we want to save homeopathy.
Homeopathic drugs will not all disappear overnight. The FDA will probably adopt a similar playbook as the one they’re using to eliminate compounded medications, employing a strategy of “death by a thousand cuts.” Slowly but surely the agency will target and eliminate homeopathic medicines one by one until it is impossible for companies to stay in business. Clearing the market in one fell swoop would create headlines; picking off medicines one by one over time allows the agency to accomplish the same goal without drawing as much attention or generating as much outrage.
Why is the FDA doing this? The agency, in attacking homeopathy, is working, once again, to protect the bottom line of drug-makers. One of the most popular uses for homeopathic medicines is for allergies. But consider that the market for Zyrtec, one of the most popular antihistamine drugs, was valued at $1.675 billion in 2021; the market for antihistamine nasal sprays is just under $2 billion. The same applies to other conditions. There’s good evidence, for example, to suggest homeopathy is effective for rheumatoid arthritis and pain management. The market for rheumatoid arthritis drugs and pain management drugs is $60 billion and $73 billion, respectively. Homeopathy cuts into these massive profits. Big Pharma and the FDA, which gets its funding from Big Pharma, want to eliminate this competition.
The FDA says it will focus on a few product categories for enforcement: those with safety concerns, products with routes of administration other than oral or topical, products to treat “serious or life-threatening conditions,” products for vulnerable populations, and products with “significant” quality issues.
We noted previously that the agency went after injectable homeopathic medicines. This means that homeopathic mistletoe for injection is on the chopping block, a safe cancer therapy that has been used for years. Studies show that mistletoe can improve symptoms and quality of life, and reduce chemotherapy and radiotherapy side effects, including in pancreatic, lung, colorectal, and breast cancers.
OTC homeopathic medicines for cold and flu, teething, allergies, and other less serious conditions that can resolve spontaneously with or without treatment are likely safe for the time being. But the FDA also notes unequivocally that, although they outline a risk-based approach, no homeopathic medicines are safe. The agency states: “However, this guidance is intended to provide notice that any homeopathic drug product that is being marketed illegally is subject to FDA enforcement action at any time [emphasis added].”
Earlier this month, we reported that the FDA was preparing to release the final version of their terrible guidance document setting forth the agency’s approach to regulating homeopathic drugs. Substantively, the final version is unchanged from the draft. The guidance declares that all homeopathic drugs are illegal because:
1. Any homeopathic drug that has not been considered “generally recognized as safe and effective” (GRAS/E) is considered a new drug; 2. FDA has not determined that any homeopathic drugs are GRAS/E; 3. A new drug cannot be marketed unless it goes through the FDA’s approval process; 4. No homeopathic drugs have gone through FDA approval.
The FDA is, and has been, out of control. It approves dangerous, expensive drugs that don’t work, and works to eliminate your access to natural alternatives to those dangerous, ineffective, and expensive drugs. The FDA doesn’t even want you learning about the benefits of natural products, lest you are persuaded to opt for medicines that are not FDA-approved drugs.
Homeopathy is used by almost 7 million Americans, who the FDA apparently thinks are not equipped to make their own healthcare choices. We need to register consumer outrage by flooding the public docket with comments demanding that access to homeopathic products—which are overwhelmingly safe—be retained.
“I’ll do one more mind experiment with you: If everyone on the planet were to get Covid and not get treated, the death-rate globally would be less than half a percent. I’m not advocating for that, because 35 million people would die.
However, if we follow the advice of some of the global leaders– like Bill Gates who said last year said “7 billion people need to be vaccinated”– then the death-rate will be over 2 billion people!
SO, WAKE UP! THIS IS WORLD WAR 3!
We are seeing a level of malevolence that we haven’t seen in the history of humanity!” Author [Censored.Ed.]
Did the regulators at the FDA know that all previous coronavirus vaccines had failed in animal trials and that the vaccinated animals became either severely ill or died?
Yes, they did.
Did they know that previous coronavirus vaccines had a tendency to “enhance the infection” and “make the disease worse”?
Did Dr Anthony Fauci know that coronavirus vaccines had repeatedly failed and increased the severity of the infection?
Yes, he did. (Fauci on ADE)
Did the drug companies conduct any animal trials prior to the FDA’s approval that would have convinced a reasonable person that the vaccines were safe to use on humans?
No, they didn’t.
Did they complete long-term clinical trials to establish whether the vaccines were safe?
No, there were no long-term clinical trials.
Did they conduct any biodistribution studies that showed where the substance in the injection goes in the body?
They did, but the data was not made available to the public.
Do the contents of the vaccine largely collect in various organs and in the lining of the vascular system?
Yes, they do.
Do large amounts of the substance accumulate in the ovaries?
Will this effect female fertility and a woman’s ability to safely bring a baby to term?
The drug companies are currently researching this. The results are unknown.
Does the vaccine enter the bloodstream and collect in the lining of the blood vessels forcing the cells to produce the spike protein?
Is the spike protein a “biologically active” pathogen?
Does the spike protein cause blood clots and leaky blood vessels in a large percentage of the people that are vaccinated?
It does, although the blood clots are mostly microscopic and appear in the capillaries. Only a small percentage of vaccinees get strokes or suffer cardiac arrest.
Should people be made aware of these possible bad outcomes before they agree to get vaccinated? (“Informed consent”)
Did the FDA know that Pfizer had “identified vaccine-associated enhanced disease, including vaccine-associated enhanced respiratory disease, as an important potential risk”?
Yes, they did, but they did not demand that Pfizer fix the problem. Here’s more:
“The FDA noted that Pfizer, “identified vaccine-associated enhanced disease, including vaccine-associated enhanced respiratory disease, as an important potential risk”. The EMA similarly acknowledged that “vaccine associated enhanced respiratory disease” was “an important potential risk… that may be specific to vaccination for COVID- 19”.
Why neither regulator sought to exclude such dangers prior to emergency use authorization is an open question that all doctors and patients are entitled to ask. Why medical regulators failed to investigate the finding that large vaccine particles cross blood vessel walls, entering the bloodstream and posing risks of blood clotting and leaky vessels is yet another open question again.” (“Open Letter to the EMA and European Parliament”, Doctors for Covid Ethics)
Did the drug companies vaccinate the people in the placebo group after the clinical trials in order to conceal the difference in the long-term health outcomes between the two groups?
That is the conclusion a rational person would make.
So, they nuked the trials?
Did the FDA largely shrug-off its regulatory duties and abandon its normal standards and protocols because
a– It wanted to rush the Covid vaccines into service as rapidly as possible? b– It knew the Covid-19 vaccine would never meet long-term safety standards?
We don’t know yet, but the adverse events report strongly suggests that the Covid-19 vaccine is hands-down the most dangerous vaccine in history.
Is the FDA rushing the “boosters” without proper testing?
Yes, it is. Here’s a clip from author Alex Berenson’s latest at Substack:
“Pfizer basically hasn’t bothered to test the booster AT ALL in the people actually at risk – it conducted a single “Phase 1” trial that covered 12 people over 65. The main Phase 2/3 booster trial (beware efforts to cover multiple “phases” of drug research at once, you want it bad you get it bad) included no one over 55.
As in NONE.” (“Are you kidding me, Pfizer, volume 1 gazillion”, Alex Berenson, Substack)
Have the boosters been modified or improved to meet the changes in Delta variant?
Is there any additional risk in taking a booster-shot after already taking two experimental gene-based vaccines in less than a year?
Considerable risk. Here’s more from the Doctors for Covid Ethics:
“Given that booster shots repeatedly boost the immune response to the spike protein, they will progressively boost self-to-self immune attack, including boosting complement-mediated damage to vessel walls.
Clinically speaking, the greater the vessel leakage and clotting that subsequently occurs, the more likely that organs supplied by the affected blood flow will sustain damage. From stroke to heart attack to brain vein thrombosis, the symptoms can range from death to headaches, nausea and vomiting, all of which heavily populate adverse reactions to COVID-19 vaccines.
As well as damage from leakage and clotting alone, it is additionally possible that the vaccine itself may leak into surrounding organs and tissues. Should this take place, the cells of those organs will themselves begin to produce spike protein, and will come under attack in the same way as the vessel walls. Damage to major organs such as the lungs, ovaries, placenta and heart can be expected ensue, with increasing severity and frequency as booster shots are rolled out.” (“Open Letter to the EMA and European Parliament“, Doctors for Covid Ethics)
So, it’s the double-whammy. On the one hand, the booster will perform largely like the original vaccine, penetrating cells and forcing them to produce spike protein which, in turn, generates blood clots and leaky blood vessels.
And, on the other, the newly-produced S proteins trigger a damaging immune response in which the complement system attacks and destroys the cells that line the inside of the blood vessels. Every additional booster will intensify this process weakening the vascular system and increasing the clotting. If the Doctors are correct in their analysis, then we could see a sharp uptick in all-cause mortality in the heavily-vaccinated countries in less than a year. Cardiac arrests are already rising.
Here’s another question that’s worth mulling over: Was there any reason for the regulators at the FDA to think that these problems would not arise following the launching of the vaccine campaign?
No. They should have known there would be problems as soon as they saw that the vaccine did not stay in the shoulder as it was supposed to. The vaccine wasn’t supposed to enter the bloodstream and spread across the body leaving billions of spike proteins in its wake. (The spike protein is a cytotoxin, a cell killer. It is not an appropriate antigen for stimulating an immune response. It is a potentially-lethal pathogen that poses a threat to one’s health even if it is separated from the virus.) Nor was the vaccine supposed to trigger Antibody-Dependent Enhancement (ADE)which is the condition we hinted at above when referring to “vaccine-associated enhanced disease”. Here’s a brief explanation:
“ADE has proven to be a serious challenge with coronavirus vaccines, and this is the primary reason many have failed in early in-vitro or animal trials. For example, rhesus macaques who were vaccinated with the Spike protein of the SARS-CoV virus demonstrated severe acute lung injury when challenged with SARS-CoV, while monkeys who were not vaccinated did not. Similarly, mice who were immunized with one of four different SARS-CoV vaccines showed histopathological changes in the lungs with eosinophil infiltration after being challenged with SARS-CoV virus. This did not occur in the controls that had not been vaccinated. A similar problem occurred in the development of a vaccine for FIPV, which is a feline coronavirus.” (“Is the Coronavirus Vaccine a Ticking-Time Bomb?”, Science with Dr. Doug)
Is this what we are seeing right now? In all the countries that launched mass-vaccination campaigns early ([Censored.Ed.], Iceland, Scotland, Gibraltar and UK) cases, hospitalizations and deaths are rising faster in the vaccinated portion of the population than the unvaccinated. Why?
Are they really experiencing a fourth or fifth wave or have the vaccines generated “inactivity-enhancing” antibodies that make the disease worse? Dr Christina Parks PhD. helps to clarify what’s going on:
“Vaccines are made to a specific variant. And when that variant mutates, the vaccine no longer recognizes it. It’s like you are seeing a completely new virus. And, because that is so, you actually get more severe symptoms when you are vaccinated against one variant and it mutates and then your body sees the other variant. The science shows, that if you get vaccinated in multiple years (for the flu), you are more likely to get severe disease, you are more likely to get viral replication, and you are more likely to be hospitalized…. We are seeing the same thing in Covid with the Delta variant. So we are actually mandating that people get a vaccine when they can actually get more sick when they are exposed to the virus…In fact, this week, a paper came out that showed that–with the Delta variant– when you are vaccinated your body is supposed to make antibodies that neutralize the virus, but they were supposed to neutralize the old variant. When they see this new variant, the antibodies take the virus and help it infect the cells.” (“Expert testimony on mandatory vaccinations”, Dr Christina Parks PhD.)
Repeat: “If you get vaccinated in multiple years, you are more likely to get severe disease, you are more likely to get viral replication, and you are more likely to be hospitalized…. With the Delta variant– when you are vaccinated …. the antibodies take the virus and help it infect the cells.”
This is ADE, and this is probably why hospitalizations and deaths are rising among the vaccinated in [Censored.Ed.], UK and the rest. True, the Delta variant is less lethal than the Wuhan virus but, unfortunately, that rule does not apply to those who have been vaccinated and whose antibodies promote the uptake of the virus into their cells. This increases the viral replication function that increases the severity of the disease. In short, people are getting sicker because they were vaccinated. Here’s another short video that helps to explain:
“…The vaccine-induced antibodies will stand up against the virus. and once a virus is under pressure; it changes, it becomes a variant, and the variant cannot be stopped by vaccine-induced antibodies.Vaccine-induced antibodies. also shut down your innate immune system… so variants can come straight through and infect those that are vaccinated. That is viral immune escape, and that means that the vaccinated are defenseless against variants. This is no longer a pandemic of Covid-19. It is a pandemic of variants…
And there is something called recombination, and recombination means a vaccinated host can be infected by more than one variant at a time. …If a vaccinated host is co-infected by more than one variant, the variants will mix DNA, and change and camouflage and produce a super variant. And if a super variants are produced, nothing can stop them. And already they are saying that the latest variant to come out is vaccine resistant. And this is just the beginning. Dr Geert Vanden Bosche warns that if we do not immediately stop mass vaccination campaigns around the world, the world will experience an international catastrophe of mass mortality. I didn’t say that, he did. The vaccinated are a threat to us all.” (“Viral Immune Escape Explained”, Dr. Michael McDowell, Rumble)
It’s not the variant that intensifies the disease, it’s the fact that the vaccine targets one narrow endpoint, the spike protein, that gradually adapts to survive. As the virus progressively learns to avoid the vaccine, vaccine-induced immunity wanes. Natural immunity produces broad, robust immunity to the whole virus not merely one part of it. It is strong and enduring.
So how will the vaccinated fight new forms of the virus, after all, the vaccine is not a medicine that overpowers a particular pathogen. It is a subtle (genetic) reprogramming of the immune system that forces one’s cells to produce a particular version of the spike protein. Boosters that stimulate production of the same protein will have only modest impact. In short, boosters are still fighting the last war.
Also, as we mentioned above, coronavirus vaccines tend to create antibodies that “enhance infectivity” when they encounter adapted forms of the virus. That means that millions of inoculated people will now face forms of the virus for which they have almost no protection and for which their compromised immune systems can only provide limited help. Here’s more from the article above:
“Right now, the fatality rate of the virus is estimated to be approximately 0.26%, and this number seems to be dropping as the virus is naturally attenuating itself through the population. It would be a great shame to vaccinate the entire population against a virus with this low of a fatality rate, especially considering the considerable risk presented by ADE. I believe this risk of developing ADE in a vaccinated individual will be much greater than 0.26%, and, therefore, the vaccine stands to make the problem worse, not better. It would be the biggest blunder of the century to see the fatality rate of this virus increase in the years to come because of our sloppy, haphazard, rushed efforts to develop a vaccine with such a low threshold of safety testing and the prospect of ADE lurking in the shadows.” (“Is the Coronavirus Vaccine a Ticking-Time Bomb?”, Science with Dr. Doug)
“Blunder”, he says?
It wasn’t a blunder. It was deliberate. The Covid-19 vaccine was supposed to fail like all the coronavirus vaccines before it. That’s the point. That’s why the drug companies skipped the animal testing and long-term safety trials. That’s why the FDA rushed it through the regulatory process and suppressed the other life-saving medications, and silenced all critics of the policy, and pushed for universal vaccination regardless of the risks of blood clotting, cardiac arrest, stroke and death. And that’s why the world is on the threshold of an “international catastrophe of mass mortality.” It’s because that’s how the strategy was planned from the very beginning.
The vaccine isn’t supposed to work, it’s supposed to make things worse. And it has! It’s increased the susceptibility of millions of people to severe illness and death. That’s what it’s done. It’s a stealth weapon in an entirely new kind of war; a war aimed at restructuring the global order and establishing absolute social control. Those are the real objectives. It has nothing to do pandemics or viral contagion. It’s about power and politics. That’s all.
Michael Whitney, renowned geopolitical and social analyst based in Washington State. He initiated his career as an independent citizen-journalist in 2002 with a commitment to honest journalism, social justice and World peace.
He is a Research Associate of the Centre for Research on Globalization.
Never mind the myocarditis and unrecorded adverse events, or the waning protection, third doses are coming … and fourth and fifth and sixth …
Mon Aug 23, 2021
(LifeSiteNews) – Not eight months after Covid-19 vaccines made their debut, hailed as a “miracle of science” and the “end of the pandemic,” it now looks like there will no end to the vaccines.
Remember when it was so important for people to get their second dose? Well now, just months later, it’s a third dose. Soon it will be so important for people to roll up their sleeve for their booster shot – for the sake of everyone’s health, of course. But no one really believes it ends with a single booster, do they?
Vaccine-maker Moderna sure doesn’t; it announced this week that it has inked a contract with the government of Canada to supply 20 million doses of its experimental mRNA shot (with an extra 15 million doses thrown in if required) for each of 2022, 2023 and 2024. Not a bad deal for your first product ever to market — and a drug that’s still in clinical trials to boot.
Especially since Moderna has some problems with the safety of its novel platform mRNA vaccine. Former New York Times writer Alex Berenson reported recently that over just three months after the launch of its novel Covid vaccine, Moderna received 300,000 reports of vaccination side effects, according to an internal report from a company that helps Moderna manage the reports. This is much higher than the numbers reported on the official government vaccine adverse event reporting system that Moderna is required by law to report side effects to.
This week, it was reported that U.S. health officials are reviewing reports that Moderna’s vaccine may be linked to a higher risk of myocarditis – an inflammatory heart condition — in younger adults than previously thought.
Heart inflammation was detected in one data set at a rate of 12.6 per million in 12-to 39-year-olds who got Moderna shots. That’s 12 times higher than the “one in a million” people are told to expect for vaccine adverse events – and it’s just one unexpected life-threatening side effects that has emerged in recent months.
Never mind. There’s 105 million doses of Moderna vaccine coming for an entire population of 37 million men, women, and children, including babies. Roll up your sleeves, Canada!
But that’s just the start. Remember way back four weeks ago when the mainstream media echo chamber was asking (as if they didn’t know the answer), if we would need an extra vaccine dose? That’s when the FDA pushed Pfizer back on its booster like a coquettish teenager and said its third dose wasn’t necessary — just yet anyway. Then it rushed headlong into the affair just weeks later. Just weeks after that, the FDA had an Emergency Use Authorization contract in hand and Pfizer had the go-ahead to start doling out its boosters in the United States in September.
Everyone knew the FDA’s pushback was a false show of refusal, didn’t they? Someone in the government of Canada sure did. Way back in April, even before Anthony Fauci began warming Americans up to the idea of booster shots, long before the whole Pfizer-FDA tango, Canadian Prime Minister Justin Trudeau announced at a press conference that his government had secured 35 million Pfizer booster shots for 2022 and another 33 million doses for 2023.
The deal had options to add 30 million doses in both ‘22 and ‘23, and an option for 60 million doses in ‘24, he told reporters.
That’s 188 million Pfizer shots. Added to Moderna’s supply that’s 293 million vaccine doses — enough injections to shoot every Canadian nearly eight times over in just three years. Do you think they might have a few booster shots a year in mind? Or are the extras for Canadian cats, perhaps?
In late July, Theresa Tam, the chief public health officer was flirting with the idea like the FDA, telling Canadians that there was “not enough data to suggest that in Canada we would go into boosting as of yet.” Two weeks later, however, shots are going into arms of “vulnerable” people in Ontario where one minister told the CBC he thinks “booster shots are going to be an important part of continuing to protect our long-term care residents. I’ve spoken to our chief medical officer about that a number of times.”
Most of Canada’s vaccine program has progressed without data though. When Canada delayed its second dose of vaccine months beyond the manufacturers’ directions, even the country’s chief scientific adviser, Mona Nemer, confessed to the CBC it was a “population level experiment.”
Then, after public health agencies worldwide suspended AstraZeneca’s vaccine when they learned it carries a risk of fatal blood clots and some people who’d already had a first dose of it didn’t want a second, Tam announced they could mix and match different kinds of vaccines like cocktails. A shot of AstraZeneca, followed by a dose of Moderna or Pfizer. This is the new freedom of choice.
Canadians soon learned that Canada’s public health progressivism was frowned upon by other countries, like the United Kingdom and cruise lines who wouldn’t accept their cocktails or let them cross their borders as if vaccinated. The World Health Organization warned that there is “limited data on the immunogenicity or efficacy of a ‘mix and match’ regimen.”
“We don’t really know the exact impacts of adding another dose to the existing schedule,” Tam admitted at a news conference. She also suggested it could be some time before the mixed shots dilemma gets resolved for the Canadians who took her advice.
“It is going to be a bit confusing and complicated in the next months ahead.”
That remark suggests it hasn’t been confusing and complicated – not to mention illogical and hypocritical – for months getting to this place.
No one seems to be asking why the miracle vaccine needs a booster dose or why, since every vaccination bar ever presented and then raised again — has been passed in Canada – and 99% of long-term care residents are vaccinated, why are heavily vaccinated Canadians – and Brits and others –locked down in a “4th wave” of COVID cases? Why is the wonder vaccine failing?
“There has been a marked decline in vaccine immunity,” one doctor wrote this week in the British Medical Journal. Pfizer claimed its vaccine was 95% effective against infection after initial clinical trials, for example, but the Mayo Clinic found that figure had dropped to 42% by July. Of course, “95% and 42% effective” refer only to the “relative vaccine effectiveness in populations,” retired pediatrician Allan S. Cunningham of Cooperstown, New York explained. The real benefit to individuals is only a tiny fraction of 1% for the prevention of serious illness caused by Covid-19.
You may want to read that again just to ensure you have understood the enormous discrepancy between what is claimed and what is real.
He also noted that the big benefits of natural and durable immunity that the United States was on the cusp of grasping was abruptly “interrupted by massive vaccine rollouts and replaced by the limited immunity from vaccines.”
“This fact is reinforced by the discovery that some of the first U.S. patients to recover from Covid-19 infections have potent antibodies against a diverse range of variants, including the Delta variant.”
He also pointed to the terrifying prospect of the immune system phenomenon called antibody-dependent enhancement of infection (ADE) from vaccines that has been seen before with dengue and respiratory syncytial virus. It occurs when vaccine antibodies actually facilitate attachment of wild viruses to cells, thereby producing more severe illness in vaccinated individuals than in unvaccinated individuals and it’s a documented risk for Covid-19 vaccines.
It’s not too late to “step back from a relentless policy of universal vaccination in the U.S. and the UK and concentrate on individuals at truly high risk,” wrote Cunningham. “This would allow the large majority of young and healthy individuals to safely acquire broad and lasting immunity from natural infections, without the risks of adverse vaccine effects, known and unknown.”
Somehow it seems that, like every reasonable and scientifically supported suggestion from thousands of doctors, scientists and other professionals such as Cunningham, this advice won’t make it to Trudeau and Tam’s booster agenda.
The pandemic will continue so long as they and the pharmaceutical giants want it to continue. Canadians and many others around the globe, including children, will be subjected to scares of variant after scary variant, long after Delta is history. When the letters of the Greek alphabet have run out, we’re told, they will start naming the new variants of Covid after the constellations of stars – Aries and Orion and Gemini Covids are to come. And experimental booster shots for each one of them.
[Editor’s Note: I’m unable to embed this video here on the site so only those who have a Facebook account will be able to view it but most people do have a FB account so please copy and paste the url that I’m posting in to your FB page and try to access what Shanon has to say. Here’s the FB url]: