webtrekker

There is, very much, a Pandemic. The Pandemic is THE CLOT SHOT bioweapons, not the supposed Sars-CoV-2. Anyone who says there is no Pandemic then go ahead and take the shots. Since no one is apparently dying then they must be safe.

Sorry for banging on about this and excuse my ignorance, but what proof is there that gain-of-function research did not produce these bioweapons?

'In a statement, Legault’s office reiterated that the codes do not contain any sensitive personal information. “The QR code sent by the Health Department contains only the name of the person, their birthday and the list of vaccines received,” the statement read.' Really? I'd have thought anyone's vaccination status was 'senstive information.'

Really? I haven't seen anything convincing to refute that yet. Have you got proof to the contrary, BC?

'US intelligence' ... another oxymoron! They know fine well the Wu-WHO-Flu was engineered by Fauci and his criminal 'gain-of-function' research to unleash an irreversible bioweapon upon the masses of the world. Even if we were to hang all of the monsters people would continue to suffer and die from the bioweapon attack. Reversal is not possible.

Stupid Reiner Fuellmich! This German idiot is confusing everyone with his so-called 'Simulation.' This has just appeared on tapnewswire and bitchute ... BREAKING – GERMANY HALTS ALL COVID-19 VACCINES, SAYS THEY ARE UNSAFE AND NO LONGER RECOMMENDED!! https://tapnewswire.com/2021/08/breaking-germany-halts-all-covid-19-vaccines-says-they-are-unsafe-and-no-longer-recommended/ Stupid, stupid man! How many people will take this seriously? He's gone way down in my estimation now.

Isn't it amazing how these feckin' Army types think they're feckin' invincible and that Joe Public won't stand a chance against them? Some big lessons tp be learned the hard way here!

Well, we all know who the true culprit is here ................................. the fucking MSM! They are the ones with the most blood on their hands, brainwashing gullible people into accepting, without question, the poisoned dart.

What cloud? I wouldn't rely on any data saved to the cloud. They can make it disappear in an instant, or even manipulate it to their own devious ends. If you are going to save anything for posterity download it and save it to permanent media such as cd or dvd.

For anyone who would rather read a breakdown of the issues covered than watch the video, here you go ... ER Editor: Stew Peters does an update on the recent FDA approval of the mRNA vaccine. These are highly technical topics, but here are some notes on what Kingston is reporting. As ever, we always recommend listening to the full interview, which runs about 27 minutes. There is some blockbuster information! *** Is the injection approved or not? There is some disagreement. Yes, Pfizer BioNTech BNT162B was approved as of August 23, 2021. What effect does this approval have on knowing what the ingredients are in the ‘vaccine’? Does information have to be released about its contents? Yes. Up to know, we haven’t known what’s in them because ‘consumer good manufacturing practices / processes’ were not being followed, which would have revealed this information, as well as the quality of the ingredients. Normally, this information is released toward the end of Phase III trials before the mass manufacturing stage. But this never happened. But it’s what’s going to be happening now. The FDA has not followed normal practices. The contents must be known in the next 2 weeks. Pfizer has been instructed to produce the list of ingredients. Other requirements are being demanded of Pfizer, too, such as consistency and quality of vials, ingredients, expiration dates (which have been constantly pushed back), adverse events / deaths, etc. All these safety protocols had been ignored until now. Re. adverse events (AE) discovered so far: there is a BREADTH of AEs that affect multiple systems in the body. Thus it appears these vials are not consistent in what they contain. So if Pfizer has not been consistent with the FDA and public over the ingredients, they have 14 days to rectify this. Do we have evidence Pfizer has not come clean over what is in the vials? Yes. The VAERS database shows an incredible diversity of AEs. How do we explain heart inflammation in young children, which might shorten their lives, or congestive heart failure immediately? Or how pregnant woman can kill their babies through breastfeeding, who have thrombocytopenia or thrombosis? Others have zero side effects whereas some have dead arm within 12 hours and can attach magnets to their bodies? None of this makes sense. The normal rate of miscarriage is 20%, but now it’s 80% in some women. How do we explain acute respiratory distress or CNS disorders such as Guillain-Barré syndrome? Normally, when a product comes out, there may be a serious AE that appears, such as heart inflammation, which means the product is recalled just because of that single symptom. The DIVERSITY of these AEs is not consistent with a consistent product. Pfizer does not have a website up: A website is ALWAYS ready to go long before a new product is launched after approval. So you’d expect one such as ‘comirnaty.com’ complete with marketing slogans and package insert information. That there isn’t one is a red flag. It suggests that Pfizer knows they’re going to be held accountable for intentionally harming people with the product AS THE MANUFACTURER. What they don’t want is charges being brought against them AS THE MARKETER. Providing they don’t put marketing materials out there, they’ll avoid a whole slew of multi-billion dollar lawsuits. Right now, they are not a marketer, so who is? Public health agencies (FDA, CDC, NIH) and the MSM. These have been the marketers to date. They have been the propagandists misleading the public. Has Pfizer violated criminal laws? Yes. As a manufacturer, they have not reported all the serious AEs and deaths through particular reporting channels available to them to the FDA. This is intentionally misinforming the FDA and the American people, so criminal charges will be filed. They do have 2 weeks to come clean as to the ingredients. A lot of information has been withheld until now, which can be construed as intentionally misleading people. What about the ‘breakout’ / ‘breakthrough’ cases? In a Mayo Clinic study, 6,000 subjects were divided into 3 cohorts: a) vaccinated with Pfizer; b) vaccinated with Moderna; c) not vaccinated. Those with one or two injections exhibited symptoms classifying them in the study as ‘breakthrough’ cases. The Mayo Clinic labelled ‘breakthrough’ cases in the following ways: people with (for example) acute kidney injury; acute thrombocytopenia (low platelet count); cardiac arrest; cardiac arrhythmia; chronic fatigue syndrome (inflammation of the CNS); encephalopathic delirium (inflammation of the brain); hypertension; fluid between the lungs and chest; sepsis (inflammation due to chemicals/spike proteins throughout the body). BUT THESE ARE ADVERSE EVENT SYMPTOMS! On Oct. 22 last year, the FDA issued a list of serious AEs to look for, which matches up with what the Mayo Clinic is now calling ‘breakthrough’ cases. Acute respiratory distress is also a symptom of ADE – Antibody Dependent Enhancement (where the antibodies raised by the vaccine INVITE IN the natural virus, making the person very sick). Basically, they’re wordsmithing with labels like ‘breakthrough’. Peters: So they’ve known about these possible symptoms and problems for MONTHS. Graphene Oxide: is it in the vaccines? Kingston: I’m as confident that G.O. is in the vaccines as I am about the existence of gravity. A Moderna patent from July 2020 (she gives the patent number) talks about 4 types of nano-lipids and the accompanying HYDROGELS, in which G.O. is highly present (according to many studies on the ingredients of hydrogels). Peters: they knew about hydrogel, myocarditis, respiratory issues, ADE, pregnancy complications and shedding all along. Shedding: In an August 2015 FDA meeting, shedding was discussed. Viral-based gene therapies were discussed, a synthetic mRNA virus which produces a spike protein. From this 2015 discussion, they knew the body would produce TRILLIONS of spike proteins in the body, which they know is toxic, as well as SHEDDING (transmitting the spike proteins to others via the mucus membranes). They knew back then, according to studies and documentation, the risks from an injected person even BREATHING on a pregnant woman. So they knew shedding was a huge risk to these women as well as their infants, and they didn’t have a way to deal with it. The FDA knew. Peters: Congress passed a law to permit this under Emergency Use Authorization. Kingston: 2 acts under Obama were passed in Congress: the PAHPRA Act of 2013 and the Cures Act of 2016. Which meant they could throw out requirements to mitigate risks for new drugs and biologics, which also included throwing out the requirement to do animal studies first, good manufacturing practices, not having to prove clinical efficacy, and INFORMED CONSENT. These Acts basically allowed the government to violate the Nuremberg Code! Congress passed laws that effectively permitted crimes against humanity on the American public Could the boosters be different in composition to what’s been approved by the FDA? Yes. (see Kingston’s discussion of Dr. Ralph Baric) Two takeaways: 1. For those nervous about taking the vaccines, we’ve won and people will be prosecuted. But take a copy of the letter (she shows the letter), which tells you that safety is unknown until 2027 for adults and children alike. Present this letter to the employer or school, saying that you’re not going to put yourself or your child at risk. 2. Whether you’re vaccinated or not, SPEAK UP. Go to local council meetings and publicly refuse to be part of this experiment.

Dr Malone Sounds Alarm on Liability Coverage of Pfizer Vaxx Dr Robert Malone, the inventor of the mRNA technology used in the COVID vaxx who has become the foremost critic of the mask and vaxx mandates, joins Steve Bannon to weigh in on the validity of the FDA’s approval of the Pfizer vaccine on Monday. He says, “The New York Times and The Washington Post got it wrong. The authorization is not for Pfizer, the authorization is for BioNTech and it will only be initiated at the time that the BioNTech-labeled product becomes available.” As Robert F Kennedy Jr writes, “There are several bizarre aspects to the FDA approval that will prove confusing to those not familiar with the pervasiveness of the FDA’s regulatory capture, or the depths of the agency’s cynicism.” Two letters sent by the FDA, one to Amit Patel at BioNTech (which contains suspicious redactions) and one to Elisa Harkins at Pfizer discuss the new branding and licensing of their vaxx, now called Comirnaty® and also state that there are “insufficient stocks” of the licensed Comirnaty®, but an abundant supply of the Emergency Use-Authorized Pfizer BioNTech product, which although “legally distinct” from one another, they both have the “same formulation” and should therefore be “used interchangeably”. As Kennedy explains, the legal distinction between the two is that the unbranded Emergency Use-Authorized COVID vaxxes still have the huge liability shield under the 2005 Public Readiness and Preparedness Act, which confers immunity from liability to everyone involved with pushing the vaxx, unless willful misconduct can be proven. He adds that no such lawsuit has ever succeeded. Under US law, these EUA products are experimental and both the Nuremberg Code and federal regulations provide that no one can force a human being to participate in an experiment and that it is unlawful to deny someone a job or an education because they refuse to be an experimental subject. So, while people have an absolute right to refuse EUA vaccines, US laws DO permit employers and schools to require students and workers to take licensed vaccines, like Comirnaty®. And Globalist puppet, Defense Secretary Lloyd Austin wasted no time in mandating vaccines for all of those in the military. The Comirnaty® product, however has no current liability shield and it is subject to the same liability laws as other products. Kennedy suspects that Pfizer is therefore unlikely to allow any American to take a Comirnaty® vaccine until it can somehow arrange immunity for it. The FDA’s weasel words are attempting to gaslight the public into letting Pfizer-BioNTech have their cake and eat it, too or as Kennedy says, https://forbiddenknowledgetv.net/dr-malone-sounds-alarm-on-liability-coverage-of-pfizer-vaxx/

You're free to think whatever you like. At least the Elite aren't controlling our thoughts yet (or are they? ). With regard to the number of Likes I receive, it doesn't bother me in the least. I just try to provide information that will get people thinking. Funnily enough, I receive most likes, as do others, for trivial Memes I post rather than actual information! Go figure!

It Begins: Die-off of the Vaccinated? https://tapnewswire.com/2021/08/it-begins-die-off-of-the-vaccinated/ Hmm, ... Strange how deaths are soaring during the Low Season for viral infections.

You really need to watch the whole video. Basically, the vax maufacturers have 14 days form the FDA approval date to list the entire contents of the 'vaccines.' Pfizer, not being the actual manufacturer (sly bastards) will still be liable to criminal prosecution. There's a lot more in the video.

Sorry for repeating this so soon but I wanted it near the top of a page as it is SO important. ** Incredible news! ** Everyone - Check this out NOW! Game up for Pfizer et al within 14 days! Former Pfizer Employee: “Checkmate. Game Over. We WIN” Biotech Analyst DESTROYS Big Pharma in BOMBSHELL EXCLUSIVE! Karen Kingston is a former Pfizer employee, a pharmaceutical marketing expert and biotech analyst. Kingston joins Stew Peters, and brings the receipts! Kingston reveals how the FDA “approval” is sure to be the “checkmate” move to end the shots that have caused unprecedented injury and death, worldwide. https://www.redvoicemedia.com/2021/08/former-pfizer-employee-checkmate-game-over-we-win/

** Incredible news! ** Everyone - Check this out NOW! Game up for Pfizer et al within 14 days! Former Pfizer Employee: “Checkmate. Game Over. We WIN” Biotech Analyst DESTROYS Big Pharma in BOMBSHELL EXCLUSIVE! Karen Kingston is a former Pfizer employee, a pharmaceutical marketing expert and biotech analyst. Kingston joins Stew Peters, and brings the receipts! Kingston reveals how the FDA “approval” is sure to be the “checkmate” move to end the shots that have caused unprecedented injury and death, worldwide. https://www.redvoicemedia.com/2021/08/former-pfizer-employee-checkmate-game-over-we-win/

Just wondering ... does anyone have any more info on the much-touted criminal proceedings supposedly being brought by Reiner Fuellmich and his cronies? We're all going to be dead before anything becomes of this!

That's a good question. I'd imagine it would be a logistical nightmare keeping those vials at such low temperatures for any length of time, while being transported all over the place.

Just passing this on ...

I've brought that up before and this was the reply ... Crazy!

Ever wondered why mRNA 'vaccines' like Pfizer and Moderna need to be kept so cold? https://www.sciencenews.org/article/coronavirus-covid-19-why-vaccines-cold-freeze-pfizer-moderna

They've even been talking on the Jeremy Vile show this morning about it being a good idea to test everyone going on staycations in the UK. Fucked if I'm going to be tested to spend a few nights in a tent!