Venera (@CDisco5) header
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Joined January 2019
Photo by Venera (@CDisco5)Photo by Venera (@CDisco5)Photo by Venera (@CDisco5)Photo by Venera (@CDisco5)Photo by Venera (@CDisco5)Photo by Venera (@CDisco5)Photo by Venera (@CDisco5)Photo by Venera (@CDisco5)
Venera retweeted
Concrete blocks to protect Christmas markets. But no concrete blocks in front of mosques. Funny, isn't it? Nobody is afraid of being run over there.
Christmas is coming and soon the Christmas markets will open. This is how we are forced to live, to prevent "someone" from driving into the crowd. Concrete blocks instead of lights. This is not freedom anymore. This is fear.
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How many millions of litres of milk do you throw away per year?
The quality milk you love made right here at home. Every day our Canadian dairy farmers produce milk according to some of the world’s highest standards, including 42 for food safety. We help feed Canada. That’s the Canadian way.

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Full breakdown of the Russell Brand verdict: youtu.be/qK8aEj3-UdY Subscribe to the podcast at fdpodcasts.com/6584/russell-… #RussellBrand #Verdict #CurrentEvents
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BREAKING NEWS: 50 year old Canadian fertility doctor Dr.Jill Griffiths died suddenly on Nov.5, 2026 She took COVID-19 Vaccines to keep her job Her Kelowna, BC Clinic "Olive Fertility Centre" pushed COVID-19 Vaccines on pregnant women: "safe for pregnant women" I broke the story of jabbed Canadian doctors dropping dead in 2022 and kept track of hundreds of these "sudden deaths". I stopped because no one in the Canadian medical community listened or cared and the abuse I got in return was simply not worth it. These deaths may be sudden but they're certainly not "unexpected" and they'll keep happening. Canadian doctor deaths rose by 53% in the first year after the jabs rolled out in 2021. I gave my data to the National Citizen's Inquiry after we downloaded records from @CMA_Docs, which buried these deaths of their own members because they had a huge Pfizer ad contract.
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Replying to @SecKennedy
7 million children poisoned with mRNA since you took office. 1/3 of parents intend on injecting their kids this year. Stop the gaslighting and excuses.
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The worst time to prepare for an emergency is when you're in the middle of one. Be prepared with @twc_health Medical Emergency Kit. Use code OMG at checkout 👇twc.health/OMG
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Inside our Next Generation Process Pilot Plant, where we test our Hydrochemolytic™ Technology on plastic waste. 👉 youtu.be/n1nCl0hrfSg Our latest campaign ran approximately 120 hours over five days, the longest we have reported and 60% longer than our 75-hour campaign in September. What it showed: ✅ Feedstock moved from controlled polyethylene and polypropylene blends (50:50, then 80:20) to PO95 for approximately 20 hours, then back to 80:20, with no complete process shutdown ✅ PO95 is a post-consumer plastic-waste agglomerate sourced from the Netherlands, containing at least 95% polyolefins, principally polyethylene and polypropylene ✅ Planned interruption tests with each feedstock. Our Operations team restored target operating conditions each time, and backup systems kept the plant running through an unexpected utility power outage ✅ Approximately 85% condensable hydrocarbon yield, in line with the campaign's performance target, with conditions set to evaluate feedstock flexibility, process stability and operating continuity rather than to maximize yield ✅ A representative wastewater sample from PO95 processing will be characterized in detail to inform treatment system design and environmental permitting This operating experience is informing equipment selection, process controls and procedures for our First-of-a-Kind Plant at @Chemelot, where engineering and permitting are underway. Full news release: investors.adurocleantech.com… #CleanTech #EcoInnovation #ChemicalRecycling #PlasticRecycling #PlasticWaste $ADUR
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Santé Canada ne procède à aucun essai visant à évaluer l’innocuité ou l’efficacité des vaccins. Il est important de comprendre que Santé Canada ne mène aucun essai sur les médicaments, y compris les vaccins, lorsqu’il s’agit de déterminer s’il convient d’approuver un médicament pour usage humain. Tous les essais sont menés par la société pharmaceutique qui a un intérêt financier à ce que le médicament soit approuvé par Santé Canada. Les vaccins contre la COVID-19 ont été exemptés de la procédure habituelle d’approbation des médicaments. Une procédure d’approbation de remplacement a plutôt été utilisée. Dans le cadre de cette procédure de substitution : 1. il n’était pas nécessaire de prouver l’innocuité; 2. il n’était pas nécessaire de prouver l’efficacité; et 3. il n’était pas nécessaire de prouver que les avantages du vaccin l’emportaient sur ses risques. Si ce critère était rempli, Santé Canada était légalement tenu d’autoriser le vaccin à des fins d’utilisation chez l’humain. Le critère en vertu duquel les vaccins contre la COVID-19 ont été approuvés est le suivant : Le ministre doit délivrer une autorisation à l’égard d’un médicament contre la COVID-19 si les exigences suivantes sont respectées : - le ministre dispose de preuves suffisantes pour conclure que les avantages associés au médicament l’emportent sur les risques, compte tenu des incertitudes relatives aux avantages et aux risques ainsi que de la nécessité de répondre au besoin urgent en matière de santé publique lié à la COVID-19. Le critère exige simplement que la société pharmaceutique demandant l’autorisation présente un argument que le ministre n’est pas tenu d’approuver. Le libellé n’est pas : - le ministre dispose de preuves suffisantes pour conclure (ce qui exigerait que le ministre soit convaincu), ni - le ministre a conclu (ce qui exigerait que le ministre soit convaincu). La formulation est plutôt la suivante : - le ministre dispose de preuves suffisantes pour étayer la conclusion (et non la conclusion du ministre). Cette formulation n’exige pas du ministre (Santé Canada) qu’il tire une quelconque conclusion. Il suffit plutôt qu’il y ait des preuves pour étayer une conclusion que le ministre ne tire pas lui-même. Pour en savoir plus : covidtestimony.com/fr/pieces…
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Play today’s challenge at allsome.app/?ref=challenge
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Allison Inquiry UPDATE: The COVID Vaccine Loophole They NEVER WANTED YOU TO SEE!!! Were Canadian children used as guinea pigs for the COVID-19 vaccines? This morning on Parliament Hill, Conservative MP Dean Allison, Shawn Buckley, and others held a press conference updating the country on the Allison Inquiry, the citizen-driven effort that gave vaccine-injured Canadians a platform in September. Over 1,400 people applied to testify; roughly 50 spoke under oath. The rest of their stories are going into the permanent record. At the press conference, it was pointed out that under the Interim Order used during COVID, pharmaceutical companies could receive approval for their COVID-19 vaccines in Canada without submitting the usual safety or efficacy data to Health Canada. While officials and media pushed the “safe and effective” message and mandates, the regulatory pathway itself required far less of the traditional evidence most Canadians assumed was mandatory. The Inquiry featured testimonies of heart damage, neurological injuries, lost careers, dismissed complaints, and ongoing struggles with the Vaccine Injury Support Program. Many were told their injuries were anxiety, coincidence, or all in their head. This was not a full parliamentary inquiry with subpoena power, but it put injured Canadians and their families on the record in the seat of power. Allison and Buckley made it clear that this is just the beginning, with talk of more town halls so additional MPs can hear these stories directly. Watch the Inquiry recordings, the press conference, and Press For Truth’s full coverage of the four days of testimony. Please SHARE THIS VIDEO FAR AND WIDE, like, comment, and subscribe to help get these voices out!!
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🇨🇦 Health Canada called Pfizer's SV40 sequence unnecessary — then kept its own review secret for three years A former government advisor calls Canada's COVID rollout a historic failure, potentially a crime against humanity, as Health Canada buried findings on Pfizer's undisclosed SV40 sequence for three years. When the general public learned that Pfizer's COVID-19 vaccine was contaminated with an undisclosed SV40 DNA sequence, @GOVCanHealth sought to have it removed. Pfizer refused, and Health Canada approved the next boosters anyway. Behind closed doors, Health Canada's own reviewers were flagging that the SV40 sequence in Pfizer's COVID-19 shot was undisclosed, unexpected and unnecessary — and the one number that would settle the safety argument is still sealed. In August 2023, Health Canada asked Pfizer to remove a genetic sequence from its COVID-19 shot. An internal note recorded the result: "as expected, Pfizer didn't commit," reviewers wrote. Weeks later, the regulator approved Pfizer's updated XBB booster anyway, with the size data on the leftover DNA not due until December, and the contamination issue persisting. It took three years, two Information Commissioner files and a Federal Court application to pry that record out of Ottawa. The sequence is the SV40 promoter-enhancer, a genetic regulatory element that acts as an on-switch for gene expression. Genomics researcher Kevin McKernan first identified it in his sequencing analysis of Pfizer and Moderna vaccine vials in 2023, a finding I exclusively reported at the time. These shots are made by growing DNA blueprints, called plasmids, in bacteria and using those blueprints as templates to manufacture mRNA. The DNA is supposed to be cleaned out. What's left behind is supposed to be capped at 10 nanograms per dose — a limit written for the animal cell lines used to make older vaccines, not for bacterial plasmid DNA wrapped in a lipid nanoparticle designed to carry genetic material into cells, as is the case with these shots. Publicly, Canadians were told the shot does not contain simian virus 40, which is technically true. In Parliament, the government called the fragment inactive with no functional role. To the Epoch Times, Health Canada said sponsors are expected to identify biologically functional sequences such as an SV40 enhancer. So which is it? The internal review answers part of that. Released only after the Information Commissioner ordered it in May 2026 and independent researcher Scoops McGoo took Health Canada to Federal Court, it confirms the sequence was not previously disclosed by Pfizer, its presence was not known or expected, and it was unnecessary. On October 6, the court recorded that Health Canada's July release had not included everything the order covered, but they weren't hit with costs and there was no penalty for their failure to comply. The section of Pfizer's report titled Characterization of Residual DNA Size Distribution remains blacked out entirely, ruled confidential business information in April 2025. Although Australia's regulator tested 28 batches and found them all under the limit, and no one has shown this DNA integrating into a human genome, there is an independent Ontario Vial Study that found lots substantially over the regulatory limit(s). While Pfizer's Canadian product monograph makes no mention of SV40 or residual DNA, it explicitly acknowledges that genotoxic and carcinogenic potential was never assessed. In other words, the monograph offers no evidence that these risks were ruled out — only that they were never evaluated. More than eight in ten Canadians took at least one shot, many from Pfizer and not necessarily out of free choice, but under the pressure of sweeping federal mandates and threats to their financial security and economic freedom. That's what Irvin Studin, a former government advisor, called the "Biggest health policy mistake in Canadian history at best, or crime against humanity at worst." Rebel News put on-the-record questions to Health Canada, the Health Minister's office, NACI, Pfizer Canada, the Privy Council Office and Justice Canada — including whether its Crimes Against Humanity and War Crimes program has received or assessed any complaint about the rollout. Justice Canada could have said no, but it didn't. Instead it hid behind a policy of never disclosing what its war crimes program does with any allegation, and the independence of prosecutors — then pointed to Health Canada as the department "best placed" to answer. The Privy Council Office pointed to the same door. Behind it: two automatic acknowledgements and silence ever since. @PfizerCA and NACI never responded at all. Eight in ten Canadians rolled up their sleeves on the promise of "safe and effective," and three years later they're still waiting to be shown the one number that would back it up
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Our NGP Pilot Plant just completed its longest campaign yet: 120 hours, including post-consumer plastic waste.

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"We'll Vax the World" was too funny!!! 😂😂 Funny enough, @AFLDSorg did our own cover of the original “We Are the World.” Not satire, just a sincere call for unity around truth, respect, medical freedom, and the doctor-patient relationship.
We'll Vax The World Starring: Everyone's favorite celebrity doctor Anthony Fauci, Francis Collins, Debrah Birx and the rest of the cast of horribles who masterminded the covid response
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At today's Allison Inquiry update, lead counsel Shawn Buckley reads out the extensive list of countries that no longer recommend the Covid-19 injection for healthy children and teens, and calls on Health Canada and the other provinces to explain why Canada continues to vaccinate this age group.
From today & it’s 5 minutes worth watching. “Are Canadian children guinea pigs for the COVID-19 vaccine?" The media buried a Provincial report that had recommended to halt COVID-19 vaccines without full disclosure & end them for healthy children and teens. Shawn Buckley reads out the long list of countries that don't vaccinate healthy kids or teens anymore with this product and they are calling on Health Canada and every other province to explain why Canada still does
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Dr. Ladapo is in a tenuous situation, waiting to see if @ByronDonalds will keep him as @FLSurgeonGen ... yet he still comes out strong against mRNA. This is integrity.
As I said in January 2024, no one should be taking mRNA COVID-19 vaccines because of their terrible safety profile. But for those who had to take one, Florida’s public health data strongly implies that thousands of Floridians died as a result of receiving Pfizer instead of Moderna. The number of lives lost in the U.S. and internationally is staggering, based on this analysis. The culture of approving vaccines without adequate safety testing and assuming “innocent until proven guilty” with these products absolutely, positively needs to end.
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The Florida vaccine study they called junk just cleared peer review. 1.47 million matched adults. Same neighborhood, same month, same kind of clinic. The only real difference was which vial they got. Over 12 months, Pfizer recipients died at higher rates than Moderna recipients on every measure. Most of the gap wasn't COVID.
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"At the press conference, it was pointed out that under the Interim Order used during COVID, pharmaceutical companies could receive approval for their COVID-19 vaccines in Canada without submitting the usual safety or efficacy data to Health Canada." Will Health Canada reply to the questions asked this morning at the Allison Inquiry press conference? @GovCanHealth @DeanAllisonMP @Shawnbuckleylaw @enqueteallison
Allison Inquiry UPDATE: The COVID Vaccine Loophole They NEVER WANTED YOU TO SEE!!! Were Canadian children used as guinea pigs for the COVID-19 vaccines? This morning on Parliament Hill, Conservative MP Dean Allison, Shawn Buckley, and others held a press conference updating the country on the Allison Inquiry, the citizen-driven effort that gave vaccine-injured Canadians a platform in September. Over 1,400 people applied to testify; roughly 50 spoke under oath. The rest of their stories are going into the permanent record. At the press conference, it was pointed out that under the Interim Order used during COVID, pharmaceutical companies could receive approval for their COVID-19 vaccines in Canada without submitting the usual safety or efficacy data to Health Canada. While officials and media pushed the “safe and effective” message and mandates, the regulatory pathway itself required far less of the traditional evidence most Canadians assumed was mandatory. The Inquiry featured testimonies of heart damage, neurological injuries, lost careers, dismissed complaints, and ongoing struggles with the Vaccine Injury Support Program. Many were told their injuries were anxiety, coincidence, or all in their head. This was not a full parliamentary inquiry with subpoena power, but it put injured Canadians and their families on the record in the seat of power. Allison and Buckley made it clear that this is just the beginning, with talk of more town halls so additional MPs can hear these stories directly. Watch the Inquiry recordings, the press conference, and Press For Truth’s full coverage of the four days of testimony. Please SHARE THIS VIDEO FAR AND WIDE, like, comment, and subscribe to help get these voices out!!
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🚨HUGE: Hedera has processed a staggering 21 MILLION transactions in just 30 DAYS! According to @chainspect_app this is an ALL TIME HIGH, $HBAR is averaging around 8 transactions EVERY SECOND, around the clock! This highlights the consistent activity on Hedera as its ecosystem expands across payments, tokenisation and enterprise applications.
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