CV19 bare essentials - STAGE1 - BARE BONES - SIMPLE BASICS
For Prophylaxis and First Day of Exposure
Immediatley Decrease your Viral Load !
Mouth wash and Nasal Rinse recommended
+ ZStack Immuno boosting nutritional substances
Buy ZStack compound from the US or buy ingredients in Oz at au.iherb.com/
For those who want to deep dive on multiple natural immuno protocols download file below. Tips and Hints given by an experienced lay person (anon)
NSW Now: Legal centre says thousands of innocent people hit with COVID-19 fines 29 September 2021
Sydney's Redfern Legal Centre says it's overwhelmed with requests for help from people who insist they have been wrongly issued with fines by police for allegedly breaching COVID health orders. The latest statistics from Revenue NSW reveal that in July and August more than 28,000 COVID fines were issued. That's about 13 times the number of fines issued during the whole of last year. The legal centre recently sent an open letter to the NSW government — signed by 100 prominent members of the legal, academic and political profession — calling for all wrongly issued fines to be revoked. The centre's senior lawyer Samantha Lee said there had been no response and called for the issue to be addressed, saying thousands of innocent people with no means of paying their fines were in distress. "Our centre has been struggling to keep up with demand to assist people who have been issued with COVID fines and what we are finding is that the majority of people have been issued with a fine unlawfully and what that means is that the police have got it wrong."
With aggressive efforts by government working with pharmaceutical corporations and medical trade groups to mandate COVID-19 vaccines and partnering with Silicon Valley and corporate media to censor public conversations about vaccination and health, it is critical for you to act now to protect your legal right to make informed, voluntary vaccine choices. Thankfully, NVIC provides the public with independent, well-referenced information on vaccines and advocates for the inclusion of vaccine safety and informed consent protections in the public health system.
Last year, NVIC sponsored the groundbreaking 5th International Public Conference on Vaccination: Protecting Health & Autonomy in the 21st Century. The conference featured 51 speakers from around the world talking about the coronavirus pandemic and defending liberty in late 2020, just before the government granted vaccine manufacturers an Emergency Use Authorization (EUA) to distribute experimental COVID-19 vaccines in the U.S. You can watch or listen to the conference for free here.
Resources Where You Can Learn More NVIC Advocacy Portal — Become a registered user of this unique free online communications network that electronically connects you directly with your own legislators and emails you action alerts with talking points so you can be an effective vaccine choice advocate in your state.
You can use it to inform your legislators about why it is necessary to protect vaccine exemptions and your legal right to make voluntary vaccine decisions for yourself and your children.
Ask 8 Vaccine Information Kiosk — Download brochures and reports on vaccination and how to recognize vaccine reaction symptoms, as well as posters and web badges that you can share with your family and friends. Access the illustrated and fully referenced “Guide to Reforming Vaccine Policy & Law” to educate your legislator when you advocate for vaccine informed consent rights.
State Law & Vaccine Requirements — You can easily obtain your state’s current vaccine policies and laws here.
Vaccine Reaction Reporting — Search for and read descriptions of vaccine reaction reports made to the federal vaccine adverse events reporting system (VAERS). Make a vaccine reaction report to NVIC.
Cry for Vaccine Freedom Wall — Read real life stories from people who have been threatened, bullied and sanctioned for trying to make voluntary decisions about vaccination for themselves or their minor children. Post your own experience.
Guide to Flu & Flu Vaccines — This “Mini Guide to influenza & Flu Vaccines” is a brief summary of facts about influenza and influenza vaccines.
COVID Jabs Are Killing Two People for Every Person Saved - Analysis by Dr. Joseph Mercola
Russel Brand Video Sept 2021
COVID Jabs Are Killing Two People for Every Person SavedAnalysis by Dr. Joseph Mercola
In the video above, Russel Brand discusses the conflicts of interest that arise when a regulatory agency is funded by the industry it is charged with regulating. Take the U.S. Food and Drug Administration, for example. In years past, the FDA was funded entirely by U.S. taxpayers.
Today, nearly 45% of its annual budget comes from user fees paid by the drug companies that seek approval for a given product, Brand says. This transition from public to corporate funding has had a significant impact on how the agency operates, and it’s clearly not in the public’s best interest.
Brand cites data showing the FDA has gone from a drug approval rate of 38% in 2005 to 61% in 2018. In situations where a drug is aimed at a disease where few medication options already exist, 89% of new drug applications are approved on the first try.
Has drug development simply gotten that much better? Probably not. The fact is that drug companies view the FDA’s user fees as payment for service rendered, and that service includes approval. They’re not paying for the FDA to turn them down.
Why FDA and Big Pharma Have a Trust ProblemIn response to the COVID-19 pandemic, the FDA issued emergency use authorizations for completely novel types of “vaccine” in a matter of weeks. While some applaud this speediness, it’s worth remembering that as speedy approvals have increased with other drugs, so have the number found to be harmful after the fact.
Data cited by Brand show that 21% of FDA approved medications ultimately had to be removed from the market or be given a black box warning. Essentially, if you’re taking a newly approved drug, the chances that this drug will be found to be extremely dangerous is 1 in 5, which is hardly encouraging!
A 2017 Yale study1 found the situation is even more dire than that, showing nearly 1 in 3 FDA approved drugs ends up having new safety issues detected in the years following approval.
The FDA is also allowing drug makers to profit at the expense of public health by allowing them to “claim success in trials based on proxy measurements instead of clinical outcomes like survival rates or cures, which take more time to evaluate,” Caroline Chen notes in a June 2018 ProPublica article.2
FDA Advisers Receive Payouts to Approve DrugsIn addition to that, “pay-later conflicts of interest” are widespread, according to an investigation by the journal Science.3 This is when doctors who advise the FDA or sit on drug panels that are in charge of drug approval are paid by drug makers AFTER the approval is a done deal.
Science examined 107 physician FDA advisers who voted on drug approvals. Of those, 40 ended up receiving more than $10,000 in post hoc earnings from the drug company whose drug they voted to approve; 26 of them got more than $100,000 and six were paid more than $1 million. FDA advisers who help drug makers gain approval also reap rewards in other ways. As noted by Science:4
“The FDA says its rules, along with federal laws, stop employees from improperly cashing in on their government service. But Science found that employees at the agency often reap later rewards — jobs or consulting work — from the makers of the drugs …
A 2016 study found that 15 of the 26 employees who left the agency later worked or consulted for the biopharmaceutical industry. Of the more than $24 million in personal payments or research support from industry to the 16 top-earning advisers, 93% came from the makers of drugs those advisers previously reviewed.”
FDA Has Already Lost Most of Its CredibilityAs argued by Brand, the data is rather unequivocal. It tells us corruption is rampant and the FDA has completely abandoned its charter to ensure public health and safety. It’s really just there to give the appearance that someone is looking out for public health, while in actuality it’s a venue through which drug makers are enabled to profit from unsafe and unproven drugs.
The sad reality is that while FDA approval used to mean something, today it has basically lost all meaning. Just because a drug is FDA-approved doesn’t mean it’s been proven safe and effective.
Again and again, drugs are found to have serious safety issues in the years after their approval. As a result, drug companies are allowed to benefit while public health is sacrificed, which is precisely the situation that the FDA was created to prevent.
FDA Approves COVID Boosters for SeniorsSeptember 17, 2021, the FDA approved the Pfizer-BioNTech COVID shot Comirnaty as a third-dose booster for people over the age of 65 and other high-risk individuals. As reported by The Vaccine Reaction September 19, 2021:5
“Despite not convening the Vaccines and Related Biologic Products Advisory Committee (VRBPAC) last month to vote on effectiveness and safety of the Pfizer-BioNTech COVID-19 vaccine (licensed under the name COMIRNATY), the U.S. Food and Drug Administration (FDA) convened the advisory committee on Friday, Sept. 17, 2021 to vote on booster doses of the vaccine.
The FDA asked the VRBPAC to vote ‘yes’ or ‘no’ on the following question: Do the safety and effectiveness data from clinical trial C4591001 support approval of a COMIRNATY booster dose administered at least six months after completion of the primary series for use in individual 16 years of age and older?
The C4591001 booster dose study did not include any subjects under 18 years of age and only 12 subjects 65-85 years of age in Phase 1 of the trial and none in Phase 2/3.”
At the end of the day, 16 of the 18 VRBPAC members voted “no” on approving a Comirnaty booster dose for people over the age of 16. A second vote was then hastily thrown together, after members indicated they’d be comfortable recommending a booster for seniors and “people at high risk of severe COVID-19,” which the FDA is defining as health care workers and those at increased risk of exposure due to their occupation.
This unscheduled second vote passed unanimously. However, as reported by The Vaccine Reaction:6
“It’s important to note the data VRBPAC was asked to consider for Vote #2 is different than for Vote #1. For Vote #2 they were instructed to consider the ‘totality of scientific evidence available’ — not just Pfizer’s booster dose clinical trial.
Had the VRBPAC been required to only consider the evidence provided by Pfizer, it would have had to base its decision on data from only 12 subjects 65 years and older in Phase 1 of the trial because they were not included in Phase 2/3. The particular evidence basis for VRBPAC’s approval of a booster dose for this group was not specified.”
What’s more, the FDA suddenly shifted from “individuals at high risk of severe COVID-19” infection, to having it apply to “health care workers or others at high risk of occupational exposure.”
“This effectively shifted the focus from those who were at high risk of become severely ill from COVID-19 to those who are simply at high risk of being exposed, which will greatly expand the scope of those recommended to have a booster dose,” The Vaccine Reaction states.7
In a September 19, 2021, appearance on CBS News,8 director of the National Institutes of Health Dr. Francis Collins stated he fully expects the FDA to extend boosters beyond seniors aged 65 and older, health care workers and others at high risk of occupational exposure.
1 in 1,000 mRNA Shots Results in Heart InflammationSo, the FDA claims the Pfizer shot is safe and effective enough to warrant a third booster for certain groups. But is it? According to a retrospective study9,10 by the University of Ottawa Heart Institute, 1 in 1,000 mRNA injections (Pfizer and Moderna) have resulted in myopericarditis, i.e., inflammation of the heart or heart sack, within one month of the shot, although symptom onset typically occurred within days.
The study was posted on the preprint server medRxiv September 16, 2021, the day before the FDA voted “yes” on boosters for the elderly and certain high-risk groups. As explained by the authors:11
“This study is a prospective collection and review of all cases with a myocarditis/pericarditis diagnosis over a 2-month period at an academic medical center … Patients were identified by admission and discharge diagnoses which included myocarditis or pericarditis. Inclusion criteria: in receipt of mRNA vaccine within one month prior to presentation …
Diagnosis was based on clinical presentation, ECG/echo findings and serial troponins and was confirmed in each case by CMR. Incidence was estimated from total doses of mRNA vaccine administered in the Ottawa region for the matching time-period. This data was obtained from the Public Health Agency of Ottawa …
Results: 32 patients were identified over the period of interest. Eighteen patients were diagnosed with myocarditis; 12 with myopericarditis; and 2 with pericarditis alone. The median age was 33 years (18-65 years). The sex ratio was 2 females to 29 males.
In 5 cases, symptoms developed after only a single dose of mRNA vaccine. In 27 patients, symptoms developed after their second dose of. Median time between vaccine dose and symptoms was 1.5 days …
Chest pain was the commonest symptom, but many others were reported. Non-syncopal non-sustained ventricular tachycardia was seen in only a single case. Median LV ejection fraction (EF) was 57% (44-66%). Nine patients had an LVEF below the normal threshold of 55%.
Incidence of myopericarditis overall was approximately 10 cases for every 10,000 inoculations. This is the largest series in the literature to clearly relate the temporal relationship between mRNA COVID vaccination, symptoms and CMR findings.”
COVID Shots May Be Killing Two for Every Life SavedAccording to expert testimony given during the September 17, 2021, FDA Vaccine Advisory Committee meeting (see video above),12 the shots may in fact be killing far more people than they’re saving.
Even if the vaccines have 100% protection, it still means we kill two people to save one life. ~ Steve Kirsch
According to Dr. Joseph Fraiman, an emergency medicine physician in New Orleans, there’s no clinical evidence to prove the COVID shots are saving more people than they harm. He told the committee they ought to:
“Demand the booster trials are large enough to find a reduction in hospitalizations. Without this data we, the medical establishment, cannot confidently call out anti-COVID-vaccine activists who publicly claim the vaccines harm more than they save, especially in the young and healthy. The fact we do not have the clinical evidence to say these activists are wrong should terrify us all.”
Steve Kirsch, executive director of the COVID-19 Early Treatment Fund, then went on to show what Fraiman feared the most, namely that the Pfizer shot kills two people for every person it saves.
“We were led to believe that the vaccines were perfectly safe, but this is simply not true. For example, there are four times as many heart attacks in the treatment group in the Pfizer 6-month trial report. That wasn’t just bad luck.
VAERS shows heart attacks happen 71 times more often following these vaccines compared to any other vaccine,” Kirsch said, adding: “If the net all-cause mortality from the vaccines is negative, then vaccines, boosters and mandates are all nonsensical.”
Here’s a screenshot from Kirsch’s slide show, showing the number of people killed by the COVID shots, compared to the number of lives saved by them.
Kirsch went on to state that while the VAERS data is the only data that are statistically significant, the other two data sources are still “troubling”:
“Even if the vaccines have 100% protection, it still means we kill two people to save one life … Four experts did analyses using completely different non-U.S. data sources and all of them came up with approximately the same number of excess vaccine-related deaths — about 411 deaths per million doses.
That translates into 115,000 people who have died (due to the Covid-19 vaccines) … The real numbers confirm that we kill more than we save. And I would love everyone to look at the Israel ministry of health data on the 90+ year olds where we went from a 94.4% vaccinated group to 82.9% vaccinated in the last four months.
In the most optimistic scenario it means that 50% of the vaccinated people died and 0% of unvaccinated people died. Unless you can explain that to the American public you cannot approve the boosters.”
Kirsch also showed data suggesting 1 in 317 boys aged 16 to 17 will get myocarditis from the shots, and after a third booster, that number may reach as high as 1 in 25. He also points out that Pfizer’s Phase 3 trials must clearly be “gamed,” as “it is statistically impossible for protocol violations to be five times higher in the treatment group.” “Why has this not been investigated?” he asked.
What Do the VAERS Data Tell Us?In a September 18, 2021, interview with The Covexit podcast, Jessica Rose, Ph.D., who holds degrees in applied mathematics, immunology, computational biology, molecular biology and biochemistry, discussed what the U.S. Vaccine Adverse Events Reporting System (VAERS) data tell us about the safety of the COVID shots.
Rose covers issues such as the magnitude of the side effects compared to other vaccination programs, the problem of under-reporting, and how causality can be assessed using the Bradford Hill Criteria. You can find a PDF of the slide show that Rose presents here.13 Here’s a summary of some of the key points made in this interview:
Between 2011 and 2020, the number of VAERS reports ranged between 25,408 and 49,412 for all vaccines. In 2021, with the rollout of the COVID shots, the number of VAERS reports have shot up to 521,667, as of September 3, 2021, for the COVID shots alone.
Between 2011 and 2020, the total number of deaths reported to VAERS ranged between 120 and 183. In 2021, as of September 3, the reported death toll had shot up to 7,662.
Cardiovascular, neurological and immunological adverse events are all being reported at rates never before seen.
The estimated under-reporting factor (URF) is 31. Using this URF, the death toll from COVID shots is calculated to be 205,809 as of August 27, 2021; Bell’s palsy 81,747; herpes zoster infection 149,017; paresthesia 305,660; breakthrough COVID 365,955; myalgia 528,457; life threatening events 230,113; permanent disabilities 212,691; birth defects 7,998.
If there’s no causal relationship between the shots and adverse events, we would expect side effects to occur at any given point between the vaccination date and symptom onset. This is not what we’re seeing. Death, for example, dramatically spikes within the first few days post-injection, and rapidly falls off after day 10.
The Bradford Hill Criteria for causation are all satisfied. This includes but is not limited to strength of effect size, reproducibility, specificity, temporality, dose-response relationship, plausibility, coherence and reversibility.
Children Are Now the Next TargetWhile the FDA voted against recommending a third booster to young adults aged 16 and over, there’s little doubt that the recommendation will soon be expanded to people under the age of 65, and eventually even young children.14 I say that because there seems to be no ceiling above which the death and disability toll is deemed too great. Why? We have not been given a straight answer, leaving us to speculate about the FDA’s intentions.
Why aren’t they concerned about safety when more than half a million side effect reports have been filed? How come nearly 15,000 reported deaths15 haven’t set off emergency alarms and in-depth investigations? As noted by Rose, 50 deaths have historically been the cutoff point at which a vaccine is pulled. We’re so far beyond that now, it seems there’s no threshold anymore.
At present, one wonders whether the FDA’s reluctance to approve a booster for younger individuals is mere show. Perhaps they’re trying to reclaim some measure of scientific authority, which was undermined by the U.S. government and Pfizer announcing the release of boosters before the FDA had even made its determination.
Whatever the case may be, I urge you to review as much data as you can before you jump on the booster bandwagon. Based on everything I’ve seen, I believe the risk of side effects is likely going to exponentially increase with each dose.
If you need a refresher on the potential mechanisms of harm, download and read Stephanie Seneff’s excellent paper,16 “Worse Than The Disease: Reviewing Some Possible Unintended Consequences of mRNA Vaccines Against COVID-19,” published in the International Journal of Vaccine Theory, Practice and Research in collaboration with Dr. Greg Nigh.
GUEST POST - i-protocol for self help - guard your health ! (authored by a mate from down under)
A Layman's Nutritional Protocol to fortify the immune system against various Viruses and Spike Proteins
These natural remedies have been shown to be effective against viral conditions. They can act preventatively as well as in the event of an infection. Make sure to have them on hand so you can increase dosing as soon as symptoms develop. The discussed supplements have a long shelf life and can remain in the medicine cupboard until needed.
We now have evidence of the latest injections containing: mRNA, spike protein, graphene oxide, SM-102, and numerous other potentially toxic substances (also: some but not all injections, appear to be higher in graphene oxide and some appear to be saline placebos).
This Nutrition protocol has been compiled to provide additional protection to those who’ve been injected with spike proteins, graphene oxide and mRNA. Said protocol is also useful to protect those concerned with the spike protein and graphene oxide shedding (transmission) coming off those who’ve been injected.
If you know someone who has been injected & requires help, pls provide them with this Nutrition Protocol, designed for discussion with a medical professional. The author remains anonymus.
Disclaimer: This is a layman's guest post and it does not provide medical advise in any form or shape. It is believed that the practice of sound nutrition and hygene empowers our natural immune system to better take care of the body. Always consult your doctor !
Andreas Kalcker Covid (MMS/CDS)
In canada they've got i think close to 2500 um fines they're fighting and here we've got dozens were fighting as well but one of the things that i've noticed since starting the civil liberties campaign which is sad because we shouldn't really have to do that that's you know there are so many civil liberties organizations which have gone silent throughout this pandemic in fact some of the human rights lawyers and civil liberties organizations are condemning people for not um accepting the vaccine mandates and and lockdowns and some of the uh restrictions that have come with it and some of the abuses of human rights that have come throughout this pandemic so we live in this weird time that uh you know news sites are the ones that are having to not only report on human rights abuses but also sorry it's not rona i promise not only report it but to also stand up and do something about it so we've we've start we've got a lot of litigation going on around the country at the moment we have the fight to find foreign i guess the one the fight defines what i want to talk about because i know we get um my inbox is full and the the revenues tips and the and the fines in boxes is full with people every day getting fines over the you know a lot of them are not even um meaning to break the restrictions it's just um they get caught out or they get put in a position where they're unable or they don't know or they don't know their rights or they or or they've read things that have given them a um a misunderstanding of the rules so i wouldn't come on here and give legal advice.
The COVID-19 shots are waking people up to vaccine myths
STORY AT-A-GLANCE (Mercola Reprint 25 Sep 2021)
This week, we celebrate our 12th anniversary of Vaccine Awareness Week. In this video, Barbara Loe Fisher, co-founder and president of the National Vaccine Information Center (NVIC) — which will celebrate its 40th anniversary as an organization in April 2022 — summarizes some of the high and low points we've experienced over the past year."It's really kind of surreal for me to watch what has unfolded since the winter of 2020," Fisher says.
"In the 1990s, I predicted that the day would come when we would not be able to function in society unless we had received every government recommended vaccine.
I didn't exactly understand how they would get there. Well, now we know how they got there, and it's like living my worst nightmare, which I thought my children and grandchildren would be grappling with after I was long gone. Instead, I'm here to witness it and it's very disturbing.
But within this difficult challenge, we also have opportunity, because I truly think that what they've done has completely changed the public's view of public health officials and of public health policy in general. And I don't think they're going to recover — perhaps ever — but certainly not for a long, long time.
The perception is that the public has not been told the whole truth about how this virus came about, and about the way in which they [need to] handle it.
Certainly, if you look at it, you see that psychological warfare has been used to create such fear and anxiety in the minds of so many people that they were willing to give up fundamental civil liberties in order to feel safe, [but it's] an illusion of safety … I think they have overreached, because they are zealots in saying that everyone should get all these vaccines in order to keep the public safe."
Growing Understanding of Vaccine DangersAccording to Fisher, polls show two-thirds of Americans do not want COVID shot mandates.1 They do not want to be required to show a vaccine passport in order to participate in society, enter a restaurant or a store, hold a job or go to college.2 "There is definitely not an appetite in this country for mandatory use of this COVID-19 vaccine," Fisher says.
[People are] starting to understand that vaccines do not prevent infection and transmission. The entire mandatory vaccination system has been built on the myth that if you get vaccinated, you cannot get infected and transmit the infection to other people. The truth is that vaccine-acquired immunity is often very temporary and sometimes you don't get it at all. ~ Barbara Loe Fisher, NVIC
An estimated 25% to 30% of health care workers and medical doctors are even refusing the COVID shot.3 As noted by Fisher, "That's quite significant, considering they're the ones who have been taking care of these [COVID] patients in hospitals." Importantly, over the past 18 months, the number of people asking questions about vaccine safety has grown significantly.
"We've been talking about these issues — vaccine ineffectiveness, leaky vaccines, as well as vaccine safety issues — for nearly 40 years," Fisher says. "So, these issues aren't just relevant for COVID. I'm hoping that this conversation is going to widen to taking a critical look at the entire mass vaccination system that is the centerpiece of public health policies around the world."
In the early 1980s, when the NVIC first started, there was no information at all for the public about vaccine risks. Doctors never discussed it, so parents knew nothing. Of course, doctors were not educated on vaccine risks either, so the ignorance was spread equally among medical professionals and lay people. Awareness about dangers has increased more or less in tandem with the expansion of the childhood vaccination schedule.
"When I came into this work, it was seven vaccines we were giving our children," Fisher says. "Tetanus, the DPT shot, measles, mumps and rubella (MMR) and oral polio vaccine. That was it. That's all the children got."
Today, children receive 72 doses of 16 different vaccines by the age of 18. The catalyst for the explosion of added vaccines in the early 1990s was the partial liability protection Congress gave vaccine manufacturers in 1986 under the National Childhood Vaccine Injury Act.
The National Childhood Vaccine Injury ActThe movie, "1986: The Act," released in 2020 explains how the National Childhood Vaccine Injury Act of 1986 (NCVIA) came about, and the ramifications of it. Fisher, who is featured prominently in the film, explains:
"That law was passed in November of 1986. I and other parents of DPT vaccine injured children worked on that law with Congress. They basically told us they were going to protect these companies from liability. We could either come to the table and argue for what we thought the children should get, or not come to the table, but they were going to pass the law.
We came to the table and did the best we could. We were just a young group of parents against the pharmaceutical industry, the medical industry and the government, that all wanted to take total liability away from these manufacturers and the doctors.
We managed to get that law to not protect the doctors. When that law was passed, the doctors were still liable for medical malpractice when it came to vaccines harming a child. The companies were also still liable for design defect. What they got off on was failure to warn.
This is what people just don't understand. They [the vaccine manufacturers] were still liable in a civil court of law. And what did [Congress] do? In December 1987, in the dead of the night, an amendment was added to an omnibus budget bill … that completely let all the doctors and vaccine providers off the hook in a civil court of law.
In hearings in 1987, companies begged Congress to give them full liability protection and Congress wouldn't do it. They only gave the doctors full liability protection.4
Our unique contribution to that law was the safety provisions: informing, recording, reporting safety provisions. VAERS is the result of what we did in insisting that there be a centralized vaccine adverse event reporting system that parents and the public could report to, as well as the doctors.
This is a one-of-a-kind vaccine adverse event reporting system [VAERS], and why we know today that more than half a million COVID vaccine reactions have been reported by the public, by doctors around this country and in other countries that use the Pfizer, Moderna and the Johnson & Johnson vaccines.
There've been more than [13,600 deaths following COVID vaccination as of August 20, 2021, and more than 55,820 post-COVID shot hospitalizations5] reported to that system."
The Destruction of the NCVIAThe National Childhood Vaccine Injury Act of 1986 also requires doctors to provide parents with written vaccine information before their children are vaccinated. Originally, these information statements were thick booklets full of information. But after the law was passed, the Department of Health and Human Services gutted the vaccine safety provisions, reducing that vaccine information statement down to a single sheet of paper.
"They took out a lot of information that should be given to parents," Fisher says. "They gutted the compensation provisions. So, today, almost no child qualifies for compensation under that law. I guess what I'm trying to say is, what the law was when it was passed is not anything like the law we see today."
Then, in 2011, the U.S. Supreme Court sided with Wyeth in a DTP vaccine injury case (Bruesewitz v Wyeth6) in which the prosecutor argued the vaccine injury was the result of a design defect (failure to make a product safer). Wyeth could have made the DPT vaccine safer, and they didn't do it. The Supreme Court majority claimed the legislative history was clear — that Congress intended that vaccine manufacturers should have no liability for FDA licensed and CDC recommended vaccines.
This was in fact the complete opposite of what the legislative history shows. Two of the Supreme Court judges, Justices Ruth Bader Ginsberg and Sonia Sotomayor, wrote a brilliant dissent, stating that the legislative history does not show that Congress wanted to give the companies complete liability protection.7
The film, "1986: The Act," dispels the myths surrounding this law, clearing up the many confusions about what the law was initially intended to accomplish. Unfortunately, the misinterpretation and gutting of the NCVIA opened the proverbial flood gates to more vaccines being mandated for children.
"There's not been one vaccine that has been created by the pharmaceutical industry and endorsed by government that has not eventually been mandated," Fisher says.
"And what they're trying to do during this pandemic is set the stage for every adult to also be required to get every government-endorsed vaccine. It is a public/private partnership between the pharmaceutical industry and government, and it's dangerous.
When I came into this work, there was somewhat of a firewall between the pharmaceutical industry and government. They're now one and the same, and Pharma calls the shots at the FDA, the NIH and the CDC. That's just the plain truth of it."
The PREP ActWhile the U.S. Supreme Court granted vaccine makers blanket immunity for childhood vaccine-related injuries by the Supreme Court in 2011, the Public Readiness and Emergency Preparedness (PREP) Act passed by Congress in December 20058 added yet another layer of liability protection for the industry. After 9/11, Congress and the pharmaceutical industry got together and passed BioShield legislation.
This federal legislation was based on the idea that weapons of mass destruction could be used against the United States, necessitating protective legislation to respond to "pandemic or bio-terrorism emergencies." Of course, the weapons of mass destruction were never actually found but, still, Congress in partnership with the pharmaceutical industry passed BioShield legislation. The PREP Act is part of that legislation.
The PREP Act has to do with declared public health emergencies such as pandemics, and includes a separate mechanism for compensation when the injury occurs from a pandemic-related medication or vaccine. The PREP Act compensation mechanism was reconfirmed by Congress in the spring of 2020, and again in March 2021,9 in regard to COVID-19.
While the 1986 National Childhood Vaccine Act-related compensation mechanism has been fatally compromised with Congressional amendments and federal agency rule making over the years, the Countermeasures Injury Compensation Program (CICP) under the PREP Act is even worse. It's so bad, if you're injured by a vaccine used under a public health emergency declaration, there's virtually no hope of compensation.
Imagine surrendering to all the pressure of losing your job and getting the jab, only to get so sick you generate over $1 million in hospital bills. It sounds outrageous, but this has in fact happened to many. They have zero recourse and in most cases have to declare bankruptcy, while the vaccine companies can continue to ravage the public treasuries without ANY liability or responsibility. It's beyond reprehensibly criminal, but they are getting away with it.
Robert F. Kennedy Jr.'s book, "The Real Tony Fauci," which comes out in November 2021, goes into far greater detail as to just how this BioShield legislation is really nothing more than a gaming of the system, essentially allowing drug companies to capture hundreds of billions of dollars from the federal government, (really you, the taxpayer). It's all a massive money and power grab.
Fauci himself, who is definitely one of the cores of this whole nightmare, is responsible for having allocated probably over $1 trillion in federal funding to researchers, principal investigators that are intimately and ultimately tied to pharma, over the 37 years he's presided as director of the NIAID. His budget for fiscal year 2021 alone is $6.5 billion.10 The patents they created generates royalties to them. It's a nightmare dystopia of raping the public from the federal treasury.
'Colossal Mismanagement of a Pandemic'From the beginning, health authorities have been neglectful when it comes to the treatment of COVID-19. They've even actively prevented safe and effective treatments from being used. In the interview, Fisher describes her own experience with COVID-19:
"I had COVID in December of 2019. I had a fairly difficult course with it for 10 weeks into the end of February of 2020. Of course, I didn't know what I had, but it was not a fun experience, and I was left with long-COVID that lasted 16 months until a functional medicine doctor who tested me found that the COVID had reactivated a [latent] Epstein-Barr infection.
She prescribed a short course of appropriately dosed ivermectin, and I had an amazing reduction in my symptoms, which included cardiac symptoms that had been diagnosed by a cardiologist. So, I had all the classic symptoms of COVID and I had a classic course of long-COVID, yet I didn't know that I could have used ivermectin months ago to help me get through.
My energy shot up after that ivermectin and I stopped having to sleep 12 hours a day. My cardiac symptoms were significantly reduced. It was like I got my life back. Yet the government has gone after doctors who have urged people to get vitamin D, vitamin C, zinc, ivermectin11 and these other licensed drugs that are safe and have been around forever.
The government actively discouraged people from doing things that could have helped them recover. This is so wrong on so many levels. It's a colossal mismanagement of an outbreak."
Of course, there are indications that it wasn't really inadvertent mismanagement but, rather, a strategic and carefully orchestrated plan to implement the Great Reset.
"A couple of months ago, I went to the website of the World Economic Forum and what comes up? The Great Reset.12 I could not believe what I was reading. It's completely transparent, how they want to reset the entire world's economy," Fisher says.
The ultimate "public health authority" is of course the World Health Organization, and the No. 1 funder of the WHO is Bill Gates, as he provides funding not only through the Bill & Melinda Gates Foundation but also GAVI.
This financial leverage gives Gates a disproportionate amount of power over public health globally and, of course, we know that his primary goal is to expand the use of vaccines. At the same time, Gates is also a major Big Tech player, which is the central enforcer of censorship. By censoring one side of the discussion, Big Tech is responsible for making informed consent impossible.
Growing Awareness That Vaccines Don't Prevent InfectionThe good news is that the COVID situation is waking people up not only to the potential dangers of these novel mRNA injections, but also to the problems and fallacies associated with all the conventional vaccines. They are starting to recognize these injections are not as harmless or as effective as they have been purported to be. That is one of the silver linings of this entire mess.
"[People are] starting to understand that vaccines do not prevent infection and transmission," Fisher says. "The entire mandatory vaccination system in this country has been built on the myth that if you get vaccinated, you cannot get infected and transmit the infection to other people; that you have vaccine-acquired immunity that is robust and contributes to herd immunity.
The truth is that vaccine-acquired immunity is often very temporary and sometimes you don't get it at all. And really, herd immunity is more based on natural immunity … So, the term 'immunization' really should never be used anymore.
These COVID 'vaccines,' the government has now acknowledged, cannot reliably prevent infection and transmission.13 This is a game-changer, if people will really get their arms around it. And so, I am glad that has come out. I'm also glad that we're seeing people around the world stand up and fight for their freedom."
The Fight for Medical Autonomy and FreedomSince the start of the COVID pandemic, the NVIC has encouraged people to work within the system, to go to your state legislators and have personal conversations with them. NVIC created model state legislation at the beginning of this pandemic, because they knew the end game would be mandatory COVID vaccination.
So far, 21 U.S. states have passed legislation that restrict or prevent COVID vaccine mandates or COVID vaccine passports. Several state governors have also issued executive orders to the same effect. These successes show us that we should not lose complete faith in the system just yet. It's broken, yes, but the answer is not to give up but, rather, to get personally involved. We need freedom-loving, rational people to get involved at every level of government, Fisher says:
"That means your school board, your county boards, city councils, your state legislatures. At the local level, you can really make a difference. Talk to your neighbors, talk to your community, give them the information that's produced by NVIC and by mercola.com.
Give them factual information backed up with references, and try to change the conversation in your community. Also, we have to change bad laws so that we won't have to feel this oppression that we've felt for almost two years …
I'll just point out, there's a page on the CDC website that basically talks about quarantine camps14 and being able to detain citizens should they feel that they need to be protected from the rest of society, or the rest of society protected from them. This is a very serious constitutional issue."
As explained by Fisher, the federal government could also invoke its authority over interstate commerce and prohibit unvaccinated people from flying from one state to another that way. There's already legislation introduced in Congress proposing this.15 So, even though 21 states have enacted laws against the requirement of vaccine passports, we're not out of the woods yet. The freedom to travel can still be stripped from us in a variety of ways, and we must fight to block all of them.
FDA's Approval of the Pfizer COVID ShotAugust 23, 2021, the U.S. Food and Drug Administration granted full approval16 to the COVID-19 mRNA injection developed by Pfizer/BioNTech, sold under the brand name Comirnaty, for use in people aged 16 and older. It's the fastest approval in history,17 and is based on just six months' worth of data from 44,060 people.18,19
Half of them got the shots and half initially received a placebo. However, in the second week of December 2020, Pfizer unblinded the control group and 93% of controls opted to get the real injection20 rather than remain in the control group for the remainder of the trial, which is slated to continue for another two years. In other words, there's no control group left against which to compare side effects and effectiveness.
The FDA was expected to hold a public meeting of the Vaccines and Related Biological Products Advisory Committee (VRBPAC)21 and allow for public and expert input before the first COVID-19 vaccine was formally licensed.
For transparency and full public disclosure of vital scientific information, this meeting should have taken place before approval because COVID-19 vaccines are the first to ever have been distributed to the US population under an Emergency Use Authorization (EUA).
In response, Robert F. Kennedy Jr. and the Children's Health Defense (CHD) filed a lawsuit22 August 31, 2021, against the FDA and its acting director, Dr. Janet Woodcock, for this mess. On its website, CHD says:
"CHD argues that the licensure was a classic 'bait and switch,' allowing Pfizer, the Biden administration, the U.S. military and employers to exhort people to take 'licensed' vaccines when in fact the vaccines available and being administered continued to be the Pfizer-BioNTech Emergency Use Authorization (EUA) vaccines …
… the FDA violated federal law when it simultaneously licensed Pfizer's 'Comirnaty' vaccine and extended Pfizer's EUA for its vaccine that has the 'same formulation' and that 'can be used interchangeably …
The law (21 U.S. Code § 360bbb-3-(3)) on 'authorization for medical products for use in emergencies' requires the EUA designation be used only when 'there is no adequate, approved and available alternative to the product for diagnosing, preventing or treating such disease or condition.'
The lawsuit alleges once the FDA approved and licensed Pfizer's Comirnaty vaccine, there was no further basis for the FDA to preserve the EUA status for the Pfizer-BioNTech vaccine that Pfizer acknowledges has the 'same formulation' and is 'interchangeable.'"
As explained by Fisher, in order to receive Emergency Use Authorization from the FDA, vaccine makers had to show their COVID jabs were more than 50% effective at preventing serious symptoms of COVID-19 disease.23 They were not required to demonstrate that the shots prevent SARS-CoV-2 infection or that it prevents transmission of the virus.
"So the bar was set very low at the very beginning for the Emergency Use Authorization," she says. "If you look at the rhetoric the CDC uses, you can see they're always talking about prevention of hospitalization and death. This is not what people think happens when you get a vaccine. We have been carefully taught to believe that when we get vaccinated, we will not get infected and we won't transmit that infection to other people."
Many Vaccines Don't Prevent Infection or TransmissionThe problem is, many vaccines don't work the way we've been told. Take the pertussis vaccine, for example. According to Fisher, there's ample evidence that you can be vaccinated against pertussis and still transmit the infection, including asymptomatically.24,25 The same thing has been shown for measles,26 mumps,27 influenza28 and chickenpox29 vaccines.
"That's why I said that this is an opportunity to educate people about what vaccination really means," Fisher says. "It's also an argument for why [COVID] vaccines should not be mandated.
In this case, it's a biological pharmaceutical product that has never been made like this. This is an entirely new technology.30 It is truly an experiment on the human race, because they did not do the kind of science that they should have done to get Emergency Use Authorization."
Dr. Peter McCullough, an epidemiologist and cardiologist who is very familiar with medical research protocols, has pointed out that none of the COVID injection trials has data safety monitoring boards. It appears standard safeguards were intentionally eliminated for the rapid rollout of these shots and to eliminate any public outcry because the incriminating data are simply not being collected.
How convenient. Actually, it is a clever strategy to achieve their goals and they are getting away with it, because those in authority do not have the courage and boldness of physician scientists like McCullough and Dr. Robert Malone, who invented the mRNA technology.31 We need 10 times more of these types of brave souls to stick their necks out, as they have the credibility to actually make a difference. We just need enough of them to take a stand.
Had proper monitoring boards been in place, McCullough believes the vaccination campaign would have been stopped by late January 2021, because of the high number of suspicious deaths that had occurred by then. There's also the possibility of these shots causing antibody dependent enhancement (ADE), which is a big concern for the future.
Watch the NVIC Conference for FREEAs you might expect, this has been an unusual year, and virtually nothing has been routine. This year, NVIC was removed from three of the four major social media platforms (Facebook, Instagram and Twitter)32 after NVIC held their groundbreaking online Fifth International Public Conference on Vaccination: Protecting Health and Autonomy in the 2st Century in late 2020.33 Fisher says:
"This year, so many people have been contacting us. We have a counseling service and we help people, families, who are going through a vaccine reaction or who are asking for information … Our weekly Vaccine Reaction newsletter has seen an almost 50% increase in subscribers, and this shows you that people are thirsty for this information.
One of the things we're really excited about is we're going to be launching a brand-new website in 2022 that your donations helped us do. It's a very expensive project, but something that I'm very excited about. We're also going to be launching an updated NVIC portal website.
We have been putting an awful lot of our efforts into the states, trying to educate people and train them on how to be effective vaccine choice advocates in their state. This takes a lot of organizing, and it takes a lot of collaboration between other groups that are on the front lines in the states.
We wouldn't be here if it hadn't been for the support that you [Dr. Mercola] have given us over the years. And I feel positive; I feel that the people in this country are going to remember that freedom is something they have to fight for. It's taken us a little bit of time to come out of our shock, because they punched us around pretty good in 2020, but I think people are waking up now and are going to start to really fight back …
Those who are authoritarian — forced vaccinators — have revealed themselves in the last 18 months. And that reveal has caused people to take a step back and look to see what their real goal is."
Take Action, Support NVIC TodayAs in previous years, during Vaccine Awareness Week, I will match your donations to the NVIC, dollar for dollar, so this is a great time to maximize your impact. So, please, consider making a tax-deductible donation to the NVIC today, and be sure to sign up for the NVIC Advocacy Portal to stay abreast of the latest legislative activities in your state.
Early treatment is vital
NAC - N-Acetylcysteine - Combat COVID-19: An Evidence Review
The novel coronavirus disease (COVID-19) is caused by a virus (SARS-Cov-2) and is known for inducing multisystem organ dysfunction associated with significant morbidity and mortality. Current therapeutic strategies for COVID-19 have failed to effectively reduce mortality rate, especially for elderly patients. A newly developed vaccine against SARS-Cov-2 has been reported to induce the production of neutralizing antibodies in young volunteers. However, the vaccine has shown limited benefit in the elderly, suggesting an age-dependent immune response. As a result,
exploring new applications of existing medications could potentially provide valuable treatments for COVID-19. N-acetylcysteine (NAC) has been used in clinical practice to treat critically ill septic patients, and more recently for COVID-19 patients. NAC has antioxidant, anti-inflammatory and immune-modulating characteristics that may prove beneficial in the treatment and prevention of SARS-Cov-2. This review offers a thorough analysis of NAC and discusses its potential use for treatment of COVID-19.
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