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Zev Zelenko, the creator of the Zelenko protocol and advocate for Hydroxychloroquine, has made a video exposing a conspiracy between Janet Woodcock and Rick Bright. Rick Bright, former head of BARDA, and Janet Woodcock, former head of Operation Warp Speed for Drugs and the FDA, allegedly conspired to restrict the use of Hydroxychloroquine to hospitals only. This strategy, implemented through emergency use authorization, hindered the timely administration of the drug. The motive behind their actions remains unclear. Rick Bright himself admitted to this conspiracy on video, claiming there was no evidence of Hydroxychloroquine's effectiveness against the virus, which is false.

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Treat COVID-19 at home with zinc and zinc-enhancing remedies like hydroxychloroquine and ivermectin, which reduce viral spread. Current protocol delays treatment until hospitalization, using ventilators and remdesivir, known to cause harm. Fauci's promotion of remdesivir, despite its lethal side effects, led to unnecessary deaths from kidney and heart failure. The true cause of death during the pandemic was not the virus but remdesivir.

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The 2018 FDA guidance recommended using drugs off-label for unmet medical needs. Hydroxychloroquine, Ivermectin, colchicine, doxycycline, Azithromycin, budesonide, prednisone, and enoxaparin were used to treat COVID-19. However, certain drugs like hydroxychloroquine faced strong opposition. Clive Palmer in Australia procured hydroxychloroquine for the entire population, but it was seized and destroyed by authorities. The motive behind targeting these drugs is unclear. If they were proven useful, there would be no need for vaccine mandates. It's questioned why people couldn't use hydroxychloroquine or Ivermectin if they were willing to try and pay for them, even if they didn't work.

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The Emergency Use Authorization (EUA) regulation from the Clinton administration included safeguards. You can distribute a medication without approval, clinical trials, or safety testing, but only if no existing approved drug is effective against the target illness. To use the EUA for vaccines, any effective drugs against COVID needed to be discredited. Early on, it was known that hydroxychloroquine was effective against coronavirus. NIH studies demonstrated its effectiveness both as a preventative and as a cure. Ivermectin was also very effective. Acknowledging that these drugs worked would have eliminated the use of the emergency use authorization. So, they had to suppress them.

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The FDA only approves emergency use authorization if there are no other alternatives. Ivermectin's effectiveness could have impacted vaccine approval. Powerful interests oppose Ivermectin due to financial reasons. Drug companies profit greatly from vaccines. Ivermectin is cheap and widely available. Merck's stance on Ivermectin changed after its patent expired. Paid articles may not always provide accurate information.

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Speaker 0: They think I'm dangerous for speaking the truth. Speaker 1: Dr. Stella Emmanuel was part of a video claiming, without evidence, that hydroxychloroquine is a cure for COVID-19. The video was taken down by social media platforms for spreading misinformation. Despite the backlash, Dr. Emmanuel insists that hydroxychloroquine could be part of a cure. Dr. Anthony Fauci disagrees, stating that scientific data consistently shows hydroxychloroquine is not effective in treating COVID-19.

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I'm Karen DeVore, a dermatologist in South Carolina. I've been prescribing hydroxychloroquine and Ivermectin for over 30 years, off-label. In 2020, the FDA called Ivermectin horse medicine and doctors couldn't prescribe it. I knew these drugs were safe and effective, and I saw great results in my patients. None of the patients I treated with these drugs were hospitalized or died from COVID. They had no side effects and felt better within hours. It's frustrating that insurance companies and pharmacies denied access to these drugs. Even terminally ill patients on ventilators couldn't try them. How many lives could have been saved?

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This year, it was revealed that $2.3 billion was allocated by the government, specifically the CDC and FDA, to pharmacies like Walgreens and CVS to discourage the prescription of ivermectin and other treatments recommended by doctors. The federal government has now acknowledged that these treatments were effective and expressed regret for suppressing them, admitting that this has led to unnecessary deaths. The influence of big pharma, particularly figures like Bill Gates, has resulted in restrictions on what healthcare professionals can prescribe, leading to consequences such as decertification and job loss for those who defy these guidelines. This situation highlights the dangers of a powerful cartel controlling medical practices.

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Manufacturers of nasal products were allegedly warned against promoting or researching their products for COVID-19. One company was allegedly denied FDA permission to study its product's effect on COVID-19. Another company, COFIX Rx, allegedly received warnings to stop promoting its product for COVID-19. The speaker claims anything that worked for COVID-19 faced strict government opposition, including hydroxychloroquine, ivermectin, and virucidal nasal sprays. Higher dose corticosteroids, zinc, vitamin D, vitamin C, quercetin, over-the-counter famotidine, and colchicine were also allegedly effective treatments. A high-quality trial allegedly showed colchicine reduced hospitalization and death, but the federal government never mentioned it. Aspirin and blood thinners were allegedly not mentioned for blood clot prevention. The speaker asserts the only advice given was to fear the virus, lockdown, social distance, wear masks, use hand sanitizer (none of which allegedly work), and repeatedly get vaccinated. The speaker concludes the COVID-19 response was allegedly about mandating vaccines.

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The speaker claims that the public had limited access to data when the vaccines received emergency use authorization. They believe regulators, who they consider corrupt, were determined to push forward with the mass vaccination program. The speaker argues that effective therapeutic medicines like Hydroxychloroquine and Ivermectin were intentionally suppressed to pave the way for vaccine authorization. They explain that a federal law prohibits emergency use authorization for a vaccine if there is an existing licensed drug that proves effective against the same disease. The speaker suggests that this decision was driven by financial interests, with the NIH owning half the patent for the Moderna vaccine and individuals associated with Anthony Fauci potentially receiving significant royalties.

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I don't speculate on the motives of individuals like Anthony Fauci or Bill Gates; I focus on their actions. The narrative reveals serious immoral behavior linked to government positions. Recently, the FDA's chief attorney acknowledged there was no justification for discouraging the use of Ivermectin, which was an effective treatment for COVID. By withholding it and other existing remedies, millions died unnecessarily. The push for vaccines was prioritized, despite a federal rule preventing emergency use authorization if effective treatments were available. This led to a lack of proper testing for vaccines, resulting in alarming health issues, particularly myocarditis in young athletes. The rising number of athlete deaths on the field is unprecedented, and there remains a need for accountability as the science continues to emerge.

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Three papers by Nathaniel Mead, containing nearly a thousand references, concluded that COVID-19 vaccination risks outweigh any theoretical benefits. According to the speaker, wishful thinking suggests vaccines saved lives and reduced severity, but early multi-drug treatment, not vaccines, reduced the risk of death. The speaker claims a marathon runner died because he didn't receive effective early treatment, and his vaccination status was irrelevant. The CDC allegedly knew that thousands of fully vaccinated patients were dying of acute COVID-19 early in 2021, making it obvious the vaccines did not reduce the risk of death. The speaker does not want America to be fooled into thinking that the vaccines save lives because they didn't.

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Tony Fauci's problem is that a federal law prohibits emergency use authorization for a vaccine if there is an approved medication that effectively treats the target disease. If Fauci or anyone had acknowledged that Ivermectin works as a treatment for COVID, the vaccine would not have received authorization. Despite many doctors and publications supporting Ivermectin, Fauci actively dismissed it as a dangerous medication to drown out its effectiveness. It is unclear why he continued to do so after receiving authorization, but there is a strong incentive for him to discredit Ivermectin and hydroxychloroquine. Notable doctors like Harvey Reich and Pierre Cory have successfully treated thousands of COVID patients.

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At home, it is recommended to treat viral replication by giving zinc and other zinc-enhancing remedies like hydroxychloroquine and Ivermectin. However, the protocol followed by hospitals was to provide no treatment until admission, and then use ventilators and Remdesivir, which were known to be harmful. Tony Fauci was aware of the dangers of Remdesivir, as it caused lethal side effects in Ebola patients. Despite this, he manipulated a study to make Remdesivir the standard of care, resulting in kidney failure, heart failure, and organ collapse in COVID-19 patients. The deaths attributed to the virus were actually caused by Remdesivir.

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Ivermectin is a widely used and safe drug that has been effective against SARS CoV 2. It could have saved many lives if it had been used more widely. Doctors who tried to use it faced prosecution, despite its safety and effectiveness. One doctor worked 715 continuous days without a day off because no one else wanted to care for indigent patients. The doctor's hospital had a low mortality rate compared to the rest of the country, thanks to protocols that included Ivermectin. However, the media ignored their success and the use of repurposed drugs. The doctor faced censorship on social media platforms for mentioning Ivermectin. The FDA claims there are no adequate alternatives to the vaccines, but many believe unnecessary deaths occurred due to censorship and lack of access to Ivermectin.

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An experimental drug called remdesivir will be responsible for people's deaths. People diagnosed with COVID-19 in the hospital died between day one and day nine, specifically on day nine of a ten-day remdesivir treatment. Dr. Anthony Fauci claimed in May 2020 that remdesivir was found safe and effective in a drug trial in Africa a year earlier (02/2019), and hyperlinked the study in a memo to hospitals. However, in that trial, remdesivir killed 53% of people, and the safety board suspended its use at month six, deeming it too deadly and toxic for Ebola patients. Dr. Anthony Fauci and his department at the NIH funded the Ebola trial in Africa in 02/2019. Therefore, Fauci lied to Congress and the American people by claiming the drug was safe and effective against Ebola, when the safety board had deemed it too deadly and pulled it from the trial.

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Ivermectin, a drug discovered in the late seventies, has had a significant positive impact on billions of people worldwide. However, it has been wrongly portrayed as a horse poison. Despite being one of the safest drugs in history, Dr. Fauci claims it is dangerous. Similarly, hydroxychloroquine is dismissed as dangerous without proper evidence. Stephen Colbert, a propagandist, dismisses the effectiveness of these drugs without acknowledging their Nobel Prize-winning status and inclusion on the WHO list of essential medicines. This misinformation is fueled by their financial ties to Pfizer, leading them to deceive the public.

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The FDA's website advises against using ivermectin for COVID-19, yet links to clinical trials, half of which indicate it may be effective. For three years, the FDA has warned against ivermectin while referencing studies that support its use. Additionally, there is increasing research suggesting ivermectin could be a vital treatment for COVID-19. The strong opposition from the federal government appears to be linked to the desire to maintain emergency use authorization for COVID vaccines. For more insights, consider subscribing for additional videos.

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Vaccines were oversold, leading to mandates that caused people to lose their jobs. The intent behind vaccine liability laws was well-meaning, but companies must be held accountable for vaccine injuries. Early treatments like hydroxychloroquine and ivermectin were undermined, preventing effective therapies from being available and allowing emergency use authorization for vaccines. This approach resulted in unnecessary loss of life. The suppression of alternative treatments benefited pharmaceutical companies financially. Despite evidence supporting treatments like corticosteroids and ivermectin, these options were dismissed, paving the way for vaccine mandates. The public response to vaccine injuries has been inadequate and unacceptable.

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A recent study claimed that 17,000 people died from Hydroxychloroquine, but Robert Kennedy Jr. pointed out flaws in the study. The drug was given to COVID patients already in the hospital instead of within the first 10 to 14 days when it is effective. The dosage administered was also much higher than recommended. While these mistakes may have contributed to deaths, it is important to consider how many lives could have been saved if the drug was used correctly. Hydroxychloroquine has been widely used for malaria and sometimes drugs are discovered to have additional benefits. The politicization of these drugs is unfortunate, especially considering their affordability.

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The forest plot shows COVID medicines, with only expensive ones approved in the US. Cheaper drugs were ignored. Studies manipulated endpoints and faced negative PR. Over 420 trials on hydroxychloroquine and 100 on Ivermectin show significant benefits, but they are dismissed in the US.

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Treat COVID at home with zinc, hydroxychloroquine, ivermectin, and other remedies that reduce viral spread. Current protocol delays treatment until hospitalization, using harmful ventilators and remdesivir. Fauci knew remdesivir's dangers from Ebola trials. He manipulated data to make it standard care, causing kidney and heart failure. Many pandemic deaths were due to remdesivir, not the virus.

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Monoclonal antibodies worked very well and quickly, and were initially readily available. The speaker believes the government intentionally made them harder to get to encourage people to take the COVID shot. The speaker started using ivermectin when monoclonal antibodies became difficult to obtain. In March, the government put out information on the FDA's website about why people should not take ivermectin for COVID. Simultaneously, the government launched COVID-nineteen Community Core on 04/01/2021, an $11,500,000,000 slush fund for propaganda.

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The FDA issues emergency use authorization for medical products when there are no approved alternatives. The effectiveness of Ivermectin as a treatment is questioned, as it would have affected the authorization of vaccines. Powerful forces with financial interests oppose Ivermectin, as it threatens global vaccination policies. Pharmaceutical companies like Pfizer, BioNTech, and Moderna have made significant profits from COVID-19 vaccines. Ivermectin is a cheap and widely available drug, but its safety is disputed by Merck, despite distributing it when it was under patent. It is important to be cautious of articles that may be biased or paid for.

This Past Weekend

Robert F. Kennedy Jr. | This Past Weekend w/ Theo Von #370
Guests: Robert F. Kennedy Jr.
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On this episode, Theo Von welcomes Robert F. Kennedy Jr., whose book The Real Anthony Fauci is a central topic of discussion. Kennedy describes his research process, including a 300‑plus‑member email list of actors, MDs, and scientists that lets him see new studies in real time and hear critical analyses of them. He argues that agency capture taints public health and environmental regulators, with the FDA funded largely by pharmaceutical companies and fast‑track approvals turning regulators into partners of industry. He contends the COVID response prioritized profits over lives, noting that early treatment was minimized and hospitalizations and ventilator use followed Fauci’s regimens. He cites hydroxychloroquine and ivermectin as effective in early treatment, says NIH studies in 2005 and later showed HCQ's potential, and accuses Gates and others of funding studies designed to discredit these drugs by using hospitalized patients and overdosing. He claims there were coercive incentives for hospitals to code deaths as COVID and to use Remdesivir, driving up counts and profits. Kennedy criticizes social and traditional media for pharma‑driven censorship, recounting his experience with Fox News where advertising revenue from pharma influenced editorial choices. He links Big Tech to the pharmaceutical industry, claiming Google and Facebook manage vaccine content and data to protect profits. He asserts direct‑to‑consumer advertising fueled this power and notes the lack of liability for vaccine manufacturers under the EUA framework, arguing that the Pfizer trial’s six‑month data showed vaccines did not clearly prevent death or transmission and appeared to increase all‑cause mortality. The discussion covers Event 201, gain‑of‑function research funded through USAID and DARPA, and the Wuhan lab network. Kennedy connects these to broader concerns about surveillance, vaccine passports, programmable money, and the erosion of civil liberties, urging three daily acts of civil disobedience to reclaim rights. He highlights autism links with vaccines in some studies and defends publishing with extensive references. The interview closes with praise for the book, a call to resist, and thanks to Kennedy for joining.
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