RefugeOfSinners

Dr Reiner Fuellmich is an experienced trial lawyer specialising in banking and stock exchange law, private international law and medical law. He is the co-founder of the Corona Investigative Committee. In this episode, we discuss the following: - Why in 2020 Dr Reiner began to look into the pandemic. - How planning for the pandemic can be traced back 10 years before it started, including a dry run at "Event 201" in September 2019. - What is the People's Grand Jury which is in progress at present, whether there is a judge and jury, what the deliverables are, who the defendants are, and whether there will be indictments and/or arrest warrants as a result of this. - Why the committee decided to instigate a People's Grand Jury investigation. - What Phase 2 will entail. - How French Lawyer Virginie de Araujo-Recchia who is part of the Grand Jury collective of attorneys was arrested on 22 March 2022 for counter terrorism and treason, what happened and whether this was an attempt to intimidate the other attorneys in France. - What happened to Christian Dettmar, the German judge who issued the ruling preventing the mandatory masking of children in schools, and whether this was designed to intimidate the German judiciary. - The advantages of the Anglo-American legal system over the German system. - What the difference is between maritime law and common law. - Whether the current legal system can be rectified. - What individual citizens can do at a local level and how can they fight back. - Whether these defendants will go in front of the International Criminal Court. - Whether they can be arrested using common law or natural law. - The prediction by Scott Ritter, (Former United Nations Weapons Inspector for the UNSCOM Mission in Iraq, former Marine Corps Intelligence Officer; USA), who was interviewed by Reiner and the Corona Investigative Committee, that the Ukraine cannot win the current war, what is happening in the Ukraine, the connection with the pandemic, and what the media is reporting. Websites referred to in the interview: - The Corona Investigative Committee website (see the Grand Jury proceedings and the Committees' weekly meetings): https://corona-investigative-committee.com/ - Statement by Maître Virginie de Araujo-Recchia on her release from custody: https://www.francesoir.fr/politique-france/virginie-de-araujo-recchia Please share this video and subscribe to our channel for more important interviews.

John O'Looney is an experienced funeral home director from Milton Keynes, England. In this episode we discuss the following: - Why the number of deaths in 2021 increased compared to 2020 and 2019. - The age groups of the deceased in 2021 resulting in more young people dying than ever before. - The cause of death as recorded by the coroners; what is stopping the coroners from recording the vaccine as cause of death? - An increase of 600% of thrombosis as the cause of death in 2021. - Why other funeral directors are not speaking out. - There was no increase in overall deaths in 2020 compared to 2019. - The use of Midazolam in aged care homes. - Feedback from the embalmer regarding unusual clotting in the deceased in 2021. - Financial incentives for the NHS for categorising COVID-19 as the cause of death. - The meeting in Westminster with Sir Graham Brady. Please share this video and subscribe to our channel for more important video interviews.

This is a clip from our interview with Brook Jackson, former Regional Director of Operations for Ventavia Research Group, turned whistleblower. To watch the full interview, visit https://rumble.com/v1fupaf-the-truth-shall-set-you-free-an-interview-with-brook-jackson.html Please share this video and subscribe to our channel RefugeOfSinners on Rumble (https://rumble.com/user/RefugeOfSinners) for more important interviews.

An interview with Brook Jackson, Warner Mendenhall and Dr Melissa McCann to discuss the status of the Brook Jackson v Pfizer case and the Australian Class Action for the vaccine injured and bereaved. Warner Mendenhall is a lawyer of 25 years and the Principal of the Mendenhall Law Group, in Ohio, USA. He has a lot of experience representing whistle blowers in the past and is part of the legal team representing Brook Jackson in the current case against Pfizer, regarding fraud in the Covid-19 clinical trial. Brook Jackson was employed by Ventavia as a Regional Director on the Phase 3 trial of the Pfizer Covid-19 vaccine, supervising two of Ventavia's three clinical trial sites. Brook filed a false claims act lawsuit on January 8, 2021. Brook is the relator and the defendants are Ventavia, Icon and Pfizer. Dr Melissa McCann comes from a pharmaceutical background and is a registered medical practitioner. She is a practice owner in the Whitsundays, Queensland, Australia. Dr McCann is bringing a class action against the TGA, John Skerritt, and the key federal Australian government officials involved in the rollout and monitoring of the covid vaccines, and the commonwealth of Australia, regarding the deaths and injuries from the novel Covid-19 vaccines. The class action consists of at least 1000 members. In this episode, we discuss the following: - When we last interviewed Warner, Brook and Robert Barnes, in mid March of 2023, they had just taken part in the motion to dismiss hearing in Texas. Judge Truncale decided to grant the motion to dismiss on the 31/3/23, after our interview. But this case is still very much alive. Warner tells us that the Judge has now overturned the motion to dismiss, and importantly allowed Brook and her lawyers to amend their claim. They are amending the complaint to add “fraud in the inducement of the emergency use authorisation at the FDA”. - We discuss how this buys time for Brook’s team, and every day that goes by, it becomes clearer the damage these shots are doing to the public. The courts are not independent of public perception. - We discuss the subject of the 170 endpoints in the Pfizer trial. Pfizer had 44 000 trial participants, and yet the efficacy calculation was only based on 170 endpoints. That’s 170 people with a positive PCR and one symptom. This is included in Brook’s claim. Brook tells us that once her 2 trial sites’ data is removed and the trial site of Augusto Roux in Argentina, then the 170 becomes a much smaller number, and Pfizer’s approval is not granted. - Fraud in the inducement - the important point here is that Pfizer knew the data was fraudulent and obtained the Emergency Use Authorisation knowing it was based on fraudulent data. - The Department of Justice requested a meeting with Brook and her team, and that was mid November, 2023. We discussed what happened and why did they want a meeting now, nearly 3 years after Brook first filed her lawsuit? It turns out that the lawyers from DOJ had no idea about the vaccine injured, and appeared to know very little regarding Pfizer’s phase 3 trial. There is a real disconnect between these DOJ attorneys, and federal bureaucrats in general and the reality of what is happening to the vaccine injured. This was just a ticking of boxes exercise by the DOJ. - We discuss the next steps in Brook’s case. Filing the amended claim, which will be December 1, then Pfizer’s response. If Judge Truncale approves, the case will go to discovery phase. - Brook tells us that her team may need $20 million for the Discovery phase. And Warner tells us that Pfizer will drag this process out as much as they can, with their huge team of lawyers. - Warner explains the unblinding that occurred in Pfizer’s trial. The unblinding was discovered by Brook at her 2 sites, and the Discovery phase will allow her team to examine all the data at the other trial sites. But the overall picture, shows that there was unblinding in totality. The unblinding led to bias. - Dr Melissa McCann gives us an overview of her case. It was filed back in April, 2023, in the NSW division of the Federal court. It now has around 1000 members, vaccine injured and bereaved. - We interviewed Dr McCann in April of this year, and you can find the interview in the references below, for a more indepth discussion of the action. - Dr McCann’s class action is not funded by the class action members. It is funded by donations. Viewers can best support Dr McCann’s class action by donating. If the case is successful, all proceeds will go to the litigants (class action members). See the crowdfunding page in the reference section below. - Dr McCann tells us about the old TGA guideline, still in place whereby the TGA must refer all serious adverse events to VSIG. She has evidence that there were no referrals to VSIG in certain covid-19 vaccine serious adverse event cases. - Dr McCann tells us it has been foreshadowed that one of or all of the following 3 things could happen in her case, in the period between December 8 and February 2024. The government lawyers could ask for; 1. a summary dismissal, or a summary judgement. 2. some or all of the pleading struck out 3. ask for a cost security. - Warner tells us there are now 238 attorneys in the Freedom Counsel, and they are filing 2 to 3 cases a week in the USA, that are Covid related. Eco Health alliance cases, employment cases (people who lost their jobs), informed consent cases, hospital death cases, vaccine injury cases. We are contemplating filing group medical malpractice cases against the hospitals. - Warner tells us that US hospitals are mandatory reporters, by law, of vaccine injury. Just like a hospital is a mandatory reporter if a child comes to a hospital and they have been abused. If the hospitals have not reported the vaccine adverse event, then they have committed a crime. The injured can file a lawsuit against the hospital. The hospitals signed a vaccine program participation agreement, they must report. - Pfizers stock price is 25% less then 5 years ago. But Pfizer has made billions from the vaccine and Paxlovid. It has been falling steeply since Nov 2022. Will there be security class action by Pfizer investors? The Brook Jackson v (Pfizer, Ventavia and Icon) References: - Refuge of Sinners interview with Brook and Warner, August 2022. https://rumble.com/v1fupaf-the-truth-shall-set-you-free-an-interview-with-brook-jackson.html - Refuge of Sinners interview with Brook, Warner and Robert Barnes, March 2023. https://rumble.com/v2d2v1s-my-god-in-whom-i-trust-an-interview-with-the-pfizer-whistleblower-and-her-l.html - The link to the Freedom Counsel discussed in this interview, which was setup after the Covid Litigation conference, back in March 2023. https://healthfreedomcounsel.com/ - Find an attorney, at Health Freedom Counsel. https://healthfreedomcounsel.com/find-an-attorney/ - Brook Jackson on X (twitter) https://twitter.com/IamBrookJackson The Australian Class Action References: - For Donations to the Australian Class Action brought by Dr Melissa McCann. The fundraiser for legal expenses for class action claims, for injuries resulting from COVID19 vaccines https://www.nomoresilenceau.com/campaigns/covid-vaccine-class-action-injuries/ - The class action filing can be seen here; https://www.covidvaxclassaction.com.au/ - For a 27 minute overview of the case by Dr McCann, you can go to her rumble channel, and the overview is here; https://rumble.com/v348nkr-covid-vaccine-injury-class-action.html - Refuge of Sinners interview with Dr Melissa McCann, April 2023. https://rumble.com/v2em0v0-what-is-impossible-for-mortals-is-possible-for-god.-an-interview-with-dr-me.html

Science Politics Faith

This is a clip from our video interview with Brook Jackson, Robert Barnes and Warner Mendenhall called "My God, in whom I trust". For the full interview, visit https://rumble.com/v2d2v1s-my-god-in-whom-i-trust-an-interview-with-the-pfizer-whistleblower-and-her-l.html Please share this video and subscribe to our channel for more important interviews.

The Voice of Truth (19 November 2021) with Dr Zev Zelenko, Prof Dolores Cahill and Craig Kelly MP, Leader of the United Australia Party. Please share this video and subscribe to our channel.

Zev Zelenko: "Joe Biden is not running the US Government" Watch the full video here: https://rumble.com/vpk7a1-the-voice-of-truth.html Please share this video and subscribe to our channel.

This is a clip from our interview with Dr Meryl Nass, former biological warfare epidemiologist. To watch the full interview, visit https://rumble.com/v1da3yp-the-lord-is-my-shepherd-an-interview-with-dr.-meryl-nass.html Please share this video and subscribe to our channel RefugeOfSinners on Rumble (https://rumble.com/user/RefugeOfSinners) for more important interviews.

This a clip from our video interview with Warner Mendenhall, Brook Jackson and Dr. Melissa McCann called "Endure to the End" For the full video interview, visit https://rumble.com/v3z43lq-endure-to-the-end-an-interview-with-warner-mendenhall-brook-jackson-and-dr..html?mref=ox58r&mc=3jwbv Please share this video and subscribe to our channel for more important interviews.

This is a clip from our video interview with Dr. Paul Marik called "God is our Anchor". For the full video interview, visit https://rumble.com/v21z0zq-god-is-our-anchor-an-interview-with-dr.-paul-marik.html Please share this video and subscribe to our channel for more important interviews.

Dr Ryan Cole is a pathologist board-certified in clinical and anatomic pathology, and is the CEO and Medical Director of Cole Diagnostics, an independent, full-service medical laboratory in Idaho. Cole Diagnostics processes and reports out approximately 40,000 blood and biopsy patient samples annually. In this episode we discuss the following: - What Dr Cole saw once the covid-19 vaccine rollout started, noting that "When a pattern changes, we pathologists are the first to see it." - How Dr Cole observed the following unusual phenomena: -- Molluscum contagiosum in elderly patients. -- Women's health biopsies, an increase in cancer. -- The decrease in ages of patients with cancer as the vaccine rolled out to younger age groups. - "Wildfire cancer": how Dr Cole observed that people with stage 1 cancer in just one organ would suddenly have stage 4 cancer everywhere else after the vaccine, caused by suppression of the immune system. - The study by Dr Fohse from the Netherlands which showed that there is a concerning alteration of the innate immune system post vaccination. - The function of the Toll-like receptors in the immune system, and how they are affected by the Covid-19 vaccine. - The Stanford University paper which showed that synthetic mRNA was persisting in patients at least 60 days after vaccination. - How Dr Arne Burkhardt showed that the spike protein was found in blood vessel walls 128 days post vaccination. - Clotting: How Dr Pretorius from South Africa showed that by adding spike protein to platelet poor plasma, clotting occurred. - How spike-mediated clots are not normal, how they are amyloid-like, which are hard to break down with the medicines we have available to us. - How doctors in Australia tell patients that the Pfizer vaccine does not cause clots, which is an absolute lie. Dr Cole outlines what tests to run to look for clotting post vaccine. - How this is "the wrong shot, wrong protein, wrong virus", how the Wuhan virus is extinct, yet the shots have not been reformulated. - How LNP (lipid nano particle) is like garlic, it goes everywhere. - The danger of taking COVID-19 vaccines while pregnant. - How there are plans to make LNP-mRNA the new delivery system for other vaccines now. Dr Cole states that this platform will probably not be ready for a decade. - The increase in all-cause mortality in vaccinated vs unvaccinated that is being reported. See Prof Norman Fenton's work. - What pathology tests patients can have done to see if their immune systems are affected by the COVID-19 vaccine. - Vitamin D, the most important conductor of your immune system. - Good Manufacturing Practise (GMP) of COVID-19 vaccines, which usually take 7 years to get completed safely for new products. Websites and papers referred to in the interview: - Dr Ryan Cole's website. https://www.rcolemd.com - K Fohse and colleagues. "The BNT162b2 mRNA vaccine against SARS-CoV-2 reprograms both adaptive and innate immune responses" https://www.medrxiv.org/content/10.1101/2021.05.03.21256520v1.full.pdf - Roltgen and colleagues, "Immune imprinting, breadth of variant recognition, and germinal center response in human SARS-CoV-2 infection and vaccination" (which shows that the vaccine’s mRNA is in human lymph nodes at least 60 days after vaccination): https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8786601/ - Pretorius and colleagues. "SARS-CoV-2 spike protein S1 induces fibrin(ogen) resistant to fibrinolysis: implications for microclot formation in COVID-19'' https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8786601/ - N. Fenton and colleagues. "Latest statistics on England mortality data suggest systematic mis-categorisation of vaccine status and uncertain effectiveness of COVID-19 vaccination" https://www.researchgate.net/publication/356756711_Latest_statistics_on_England_mortality_data_suggest_systematic_mis-categorisation_of_vaccine_status_and_uncertain_effectiveness_of_Covid-19_vaccination - Professor Norman Fenton's website, and the webpage listing his COVID-19 publications. https://www.normanfenton.com/covid-19 Please share this video and subscribe to our channel RefugeOfSinners on Rumble (https://rumble.com/user/RefugeOfSinners) for more important interviews.

Jaana Pitkanen is a nurse from Queensland, Australia with 31 years experience. Here she tells her story from inside two major hospitals of their COVID response and the story of the COVID vaccination injured patients. Hear first hand how the hospital staff were asked to only get their covid19 information from government supplied websites, and given a computer application to ensure they could only access approved sites. Jaana describes the vaccine injuries and how COVID vaccination status is not recorded when the injured patients arrive and injuries are not recorded as vaccine induced. Please share this video and subscribe to our channel.

This is a clip from our interview with Dr Ryan Cole, CEO and Medical Director of Cole Diagnostics. To watch the full interview, visit https://rumble.com/v14u78z-speak-the-truth-in-love-an-interview-with-dr-ryan-cole.html Please share this video and subscribe to our channel RefugeOfSinners on Rumble (https://rumble.com/user/RefugeOfSinners) for more important interviews.

For the full interview, visit https://rumble.com/vqrlzk-fear-not-part-one.html Please share this video with others and subscribe to our channel.

Sasha Latypova holds a graduate degree in business from Dartmouth College and is a retired pharmaceutical industry, research and development executive with 25 years of experience in conducting clinical trials. In this episode, we discuss the following: - Sasha did not work for a pharmaceutical company, she contracted to pharma companies. She conducted clinical trials in imaging, and later in cardiovascular safety monitoring. Most companies now outsource their clinical trials to contractors, like Sasha. So, Sasha was responsible for being in compliance to the regulators at all times, when conducting these trials. She is aware of all the regulations. - Sasha retired from her work in the pharmaceutical industry before the Covid19 period began. We discuss why she became interested in the Covid situation, both the early treatment and the new vaccines. - Sasha first became suspicious when the public health officials started to suppress hydroxychloroquine, as she had experience with this drug. They tried to smear this drug with cardiovascular arrythmia, which she was familiar with in her previous work. She knew for sure that hydroxychloroquine did not have that problem, especially when take for a short time frame, as it was for Covid. - She was the first to notice the batch variability of Covid vaccine adverse events in VAERS. Sasha collaborated with Craig Paardekooper on the website “How bad is my batch”. She knew right away that these products were not Good Manufacturing compliant. This was her conclusion by October 2021. She wrote letters to the CDC and FDA about this. Senator Johnson brought this data to the attention of the CDC and FDA also. The CDC and FDA never did anything. - At the end of 2021, Mike Yeadon sent Sasha a package of leaked documents from the EMA, about 800 pages worth, and a dozen emails between the regulators (EMA, MHRA, FDA). This package was actually leaked around Nov 30, 2020. It was clear from these documents, that this drug product was substandard, and the worse product she had ever seen. The bulk of the documents were from EMA regulators themselves. - Sasha tells us the number one thing that the regulators have to approve is the manufacturing. If you can’t manufacture, then safety and efficacy doesn’t matter. And yet all the scientists and doctors are focussing on safety and efficacy and no one is looking at manufacturing. The EMA documents showed evidence that the EMA regulators had raised 100 major objections to the approval of the Pfizer product. - An example of an objection. Pfizer had provided no evidence they were making the spike protein. And, we later learnt they faked the Western Blots, which was an assay to characterise the spike protein. It was a computer generated fake. - Sasha shows us the 3 drug approval pathways that are relevant to the approval of the vaccines in the USA. The normal FDA regulatory pathway for market approval. The Expanded Access Use pathway. The Emergency Use Authorisation pathway, and she explains the differences. There was a lot of confusion, and many people thought the Emergency Use Authorisation (EUA) was in fact the Expanded Use pathway, but they are very different. - The EUA comes under a brand new paragraph of the Food, Drug and Cosmetic Act, called Paragraph 564. EUA countermeasures can only be issued when the HHS has declared a public health emergency. And they are designated as non investigational. And so none of the laws that normally apply to drugs apply to these countermeasures. EG No IRB (investigational review board), no informed consent for recipients, and good manufacturing practise is not enforced. The only criteria needed, is that the HHS secretary thinks they may be effective. - For an in depth explanation of the legal framework, there is a good video of Sasha and Katherine Watt (the US para legal who worked with Sasha), explaining all the legal codes that were put in place in the USA, in the years preceding 2020. Sasha explains it took 3 years to unravel all the legal codes around this. See reference below. - Sasha shows us the transcript of a meeting, in which Doran Fink (deputy director of Vaccines and Related Biological Products Advisory Committee (VRBPAC) in the FDA, on Oct 22, 2020, stated that the FDA decided to use the EUA pathway rather then the expanded access use for approval of the Covid vaccines. And the reason was that expanded use required IRB and informed consent. That would add complexity. See Reference below. - Doran Fink is now at Moderna. - Sasha shows us the Pfizer timeline, showing the activity in terms of approvals etc from March 2020 through to Dec 2024. She points out that Doran Fink says they switched to EUA in Oct 2020, but she believes that in fact the switch happened in July 2020 as that is when Pfizer began mass producing the 30 million doses for the rollout. And, as we discuss, this was before phase 3 even started and before FDA approval of the product . That would have been illegal under IND. - In addition, the formula for the product was changed 5/6 times during the phase 3 trial ie they changed which drug they were testing. This was found in the 1100 page protocol document. - The FDA issued a BLA (Biologics License Application) in August 2021. So everyone thought the Pfizer vaccine was fully approved. But Sasha shows us the BLA letter, and it references the 2 Pfizer clinical trials, the Phase1/2 trial and the phase 3 trial, which were NOT clinical trials. So the BLA is fake, its illegal and the FDA is certifying the fraud. That’s why there are 2 products, but in the USA they never shipped the Comirnaty product , only the EUA product (Biontech). - Sasha explains that as long as the PREP Act is in place, these products “will not be deemed adulterated or misbranded”, and shows us the excerpt from the US code. This is why there is no enforcement of good manufacturing practise. - We discuss the involvement of the US Department of Defence. The DOD is the CEO of the operation , is totally in charge, and HHS has only an advisory role. The money all came from the DOD. - Sasha reveals that she has an audio of a discussion at a pharma company regarding a phone call that they received on Feb 4, 2020 from DOD. The DOD told them on that day, to switch from pan influenza (they were part of the P3 consortium) to Covid as Covid had been classified as a national security threat. See references. - What is the Pandemic Preparedness Program (P3), which was started in 2017. The person in charge of P3 is Colonel Matt Hepburn, and he is the mastermind. He has published TED talks on P3, and has claimed we can predict viruses and we will make vaccines in hours. - We ask Sasha who she thinks is behind the release of the virus and the injections. Websites referenced in the Interview; - Sasha Latypova’s Substack, which is called Due Diligence and Art. https://sashalatypova.substack.com - Video discussion between Katherine Watt and Sasha Latypova explaining the US Legal codes and the forensic work done by Katherine to uncover how the EUA was created. https://rumble.com/v3udbi4-sasha-latypova-and-katherine-watt-talking-about-non-regulation-of-non-medic.html -Doran Fink at VRBPAC meeting Oct 22, 2020. The entire transcript is here. Go to page 203 to see the answer by Doran Fink. https://www.fda.gov/media/143982/download - A good place for new readers to start. A summary of Everything - End 2023. https://sashalatypova.substack.com/p/summary-of-everything-and-quick-links - Audio Leak from pharma company regarding Feb 4, 2020 call from DOD. https://sashalatypova.substack.com/p/audio-leaked-from-astrazeneca-covid

Heroes of the Southern Cross (15 October 2021) Please subscribe to our channel and share this video with others. You can follow our guests at the following links: Mack - https://t.me/NationalEducationUnited Craig Backman - https://www.facebook.com/profile.php?id=100073863272525 Graham Hood - https://rumble.com/user/RoyalAustralian https://t.me/Grahamhoodformerpilot1 John Larter - https://t.me/johnlarter Craig Kelly - https://youtube.com/c/UnitedAustraliaPartyUAP https://t.me/craigkelly

Brook Jackson has worked in the clincial trials field for over twenty years. Brook is a Clinical Research Auditor and Certified Clinical Research professional. Before working for Ventavia Research Group, Brook served as the Director of Operations for a multi-state clinical trial company. Brook began her employment with Ventavia on September 8, 2020 as a Regional Director on the Phase 3 trial of the Pfizer Covid-19 vaccine, supervising two of Ventavia's three clinical trial sites. Warner Mendenhall is a lawyer of 24 years and the Principal of the Mendenhall Law Group, in Ohio, USA. He has a lot of experience representing whistle blowers in the past and is part of the legal team representing Brook Jackson in the current case against Pfizer, regarding fraud in the COVID-19 clinical trial. In this episode we discuss the following: - What was Brook's role as Regional Director at Ventavia. - We discuss the basic concepts of a Phase 3 clinical trial of a drug product including what is a double blind randomised controlled trial. - Brook outlines what she saw once she started work at Ventavia, including the following flaws in the trial process there, including: * The unblinding of all trial participants from July to September 2020. * Failure by Ventavia staff to follow the correct informed consent procedure. * Failure to obtain all the signatures required from trial participants, and in some cases the forging of participant signatures. * Failure to properly describe the adverse event reporting procedures to triallists. * Failure to keep the drug product at the required cold temperature. * Failure to quarantine drug product that was not kept at appropriate temperature. * Failure to record adverse events correctly. - Brook explains that when the unblinding error was discovered, the Ventavia staff were asked to remove the evidence and lie to Pfizer about the unblinding. - Ventavia was understaffed and under pressure to onboard a large number of triallists. Why the rush, what is the payment criteria from Pfizer? Is Ventavia paid per triallist? - Ventavia has been rewarded by Pfizer with 4 more contracts for clinical trials on the Pfizer Covid-19 vaccine (Covid-19 vaccine in children and young adults, pregnant women and a booster dose). - Brook reported her concerns to Ventavia, and then anonymously also to Pfizer. After neither company acted, Brook reported her concerns to the FDA. The FDA did not inspect the Ventavia sites. Ventavia fired Brook on the same day that she made her report to the FDA. - The Director of Operations at Ventavia contacted Brook in June 2021, she had been fired in 2021 for bringing forward the same concerns as Brook. - Brook filed a false claims act lawsuit on January 8, 2021. The plaintiff is the United States of America, with Brook Jackson as the relator. The defendants are Ventavia, Icon and Pfizer. - Warner Mendenhall explains the Qui Tam action. - The lawsuit went under seal for 6 months. The US government chose not to join the lawsuit, and it was not unsealed until February 2022. - Brook's original lawyers warned Brook that "they (the government) will come after you", when she requested to speak out to save lives. - Warner explains what the possible financial penalties are for Pfizer if Brook's case is successful. - Pfizer have filed a motion to dismiss the lawsuit, claiming that in their contract with the US Department of Defence, they have only committed to produce a prototype. - Warner discusses what is the essence of the bargain between Pfizer and the US government. Documents referenced in the interview: - The False Claims Act Lawsuit, USA ex rel Brook Jackson vs Ventavia Research Group, Pfizer, Icon. https://www.documentcloud.org/documents/21206071-brook-jackson-lawsuit https://www.academia.edu/71772143/US_District_Court_for_Eastern_Texas_USA_ex_rel_Brook_Jackson_v_Ventavia_Research_Group_recently_unsealed_qui_tam_action_against_vaccine_entities_Pfizer_Inc_Icon_PLC_and_Ventavia_Research_Group_LLC - "Covid-19: Researcher blows the whistle on data integrity issues in Pfizer’s vaccine trial". The British Medical Journal Investigation. https://www.bmj.com/content/375/bmj.n2635 Please share this video and subscribe to our channel RefugeOfSinners on Rumble (https://rumble.com/user/RefugeOfSinners) for more important interviews.

This is a clip from our interview with Dr Ryan Cole, CEO and Medical Director of Cole Diagnostics. To watch the full interview, visit https://rumble.com/v14u78z-speak-the-truth-in-love-an-interview-with-dr-ryan-cole.html Please share this video and subscribe to our channel RefugeOfSinners on Rumble (https://rumble.com/user/RefugeOfSinners) for more important interviews.

Dr Sucharit Bhakdi has a medical degree, is a Professor of Microbiology and has published over 300 articles in the fields of immunology, bacteriology, virology and parasitology. He chaired the Institute of Medical Microbiology and Hygiene at the Johannes Gutenberg University of Mainz, Germany from 1990 until his retirement in 2012. In this episode we discuss the following: - Why Dr Bhakdi stated in the December 2021 paper authored with Dr Arne Burkhardt that the current covid19 vaccines cannot protect against viral infection. - The metaphor of the airforce and navy defence in our immune systems. - The fundamental design flaws of the vaccines. - The second part of the paper with Dr Arne Burkhardt concerns the autopsy that he conducted of 15 vaccinated patients who died after the Covid-19 vaccinations. Dr Burkhardt performed histo pathological analysis and proved that 14 of the 15 deaths were caused by the vaccination. The conventional autopsies for the 15 had found no connection. What did he find? - Was the authorisation of these vaccines based on fraudulent data, therefore protection against liability lost? - Dr Bhakdi presented the findings of Dr Burkhardt at a Symposium in December 2021 and yet the Covid-19 vaccines were not retracted. - What is unique about these auto immune reactions which was found by Dr Burkhardt which also clearly indicates that the vaccines are the cause of the injury. - Lymphocytes are attacking their brothers and sisters, this creates immune deficiency. What percentage of the lymphocytes are destroyed? - The pandora's box metaphor explained and its ramifications. - In the Cell paper, the vaccine's mRNA was found in the human lymph nodes at a minimum of 60 days after vaccination. See figure 7. - A new paper has been published proving that the vaccine's mRNA could be translated back to our 'book of life' (the DNA in our cells). - People ask "Why have the doctors not spoken out?''. Dr Bhakdi and a group of doctors did speak out . A letter to the EMA dated February 2021 regarding Covid-19 Vaccine safety concerns was sent and can be found on the doctors4covidethics.org website. What was the reply from the EMA (European Medicines Agency)? - Dr Bhakdi and Dr Burkhardt and their new pathology project. - Will these gene therapy vaccines have their authorisations removed? - Dr Bhakdi spoke at a rally in Austria earlier this year. What has happened in Austria since then? - Paul Ehrlich Insitute in Germany, the role of this institute and the qualifications of the head of the institute. ********** Papers and websites referenced by Dr Bhakdi throughout the interview: - Dr Bhakdi and Dr Burkhardt - On Covid vaccines - why they cannot work and irrefutable evidence of their causative role in deaths after vaccination. Dec 2021. https://doctors4covidethics.org/on-covid-vaccines-why-they-cannot-work-and-irrefutable-evidence-of-their-causative-role-in-deaths-after-vaccination/ - Dr Burkhardt - Notes on conducting post mortem autopsy of persons connected with Covid vaccination. March 2022. https://doctors4covidethics.org/notes-and-recommendations-for-conducting-post-mortem-examination-autopsy-of-persons-deceased-in-connection-with-covid-vaccination-updated/ - The new Cell paper from Stanford University, Jan 2022, which shows the vaccine’s mRNA lasting in human lymph nodes for at least 60 days post vaccination. Refer to Figure 7. ''Localization of SARS-CoV-2 proteins and vaccine mRNA in LNs'' Roltgen and colleagues, "Immune imprinting, breadth of variant recognition, and germinal center response in human SARS-CoV-2 infection and vaccination" https://www.cell.com/cell/fulltext/S0092-8674(22)00076-9 - Alden and colleagues. "Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line" https://www.mdpi.com/1467-3045/44/3/73/htm - First letter to the EMA from the Doctor for Covid Ethics Group. Feb 2021. https://doctors4covidethics.org/urgent-open-letter-from-doctors-and-scientists-to-the-european-medicines-agency-regarding-covid-19-vaccine-safety-concerns/ ********** Please share this video and subscribe to our channel for more important interviews.

Dr Paul Marik is a Pulmonary and Critical Care Specialist, originally from South Africa. He was Chief of Pulmonary and Critical Care at Eastern Virginia Medical School. He developed a life saving protocol for sepsis. He has written over 400 peer reviewed journal articles and has been cited over 35 000 times in peer reviewed publications. He is the second most published critical care physician in the world. He is the co-founder of the FLCCC (Front Line Covid-19 Critical Care Alliance). In this episode, we discuss the following: - Why was the FLCCC created. - Dr Marik tells us that if the early treatment protocol suggested by the FLCCC had been adopted widely and accepted by the agencies, by now this would all be over. Instead, the measures adopted by the agencies have made things significantly worse. - Dr Marik tells us that we now have a humanitarian disaster of unbelievable proportions, which is the Covid-19 vaccine injured. According to the V-safe data, there are 18 million Vaccine injured Americans. - Vaccine injury is a complex disease, the average number of symptoms per patient is 23. - Dr Marik tells us that his organization now has assessed that there are 2 spikes of death. One is in the first 10 days after the injection. The second spike of death is 5 months after the injection. - What is in the FLCCC’s vaccine recovery protocol. What is autophagy? - Dr Marik tells us that ivermectin is from nature, and nature does not make mistakes. We discuss the Australian ban of ivermectin. - We discuss the lawsuit against the FDA regarding their ivermectin advice. - What is the Federation of State Medical Boards. A secret organization. How much power do they have? - Dr Marik discusses the lack of efficacy of Tamiflu for influenza and molnupirivir for Covid-19. - Why in 2020 did the US health authorities suppress early treatment for Covid-19? - What would Dr Marik like to see changed in America with respect to the FDA and the CDC to stop this corruption around protocols for disease and vaccine approval. - Dr Marik tells us that medical schools get funding from the NIH. They are no longer places of independent education and independent thought. If they do not follow NIH guidelines they do not get funding. Websites referenced in the Interview - The Front Line Covid-19 Critical Care Alliance (FLCCC) website: https://covid19criticalcare.com/ - The 4 protocols for Covid-19 treatment; early treatment, hospital treatment and long haul syndrome and post vaccine inflammatory syndrome. https://covid19criticalcare.com/covid-19-protocols/ - C19 website. (listing all the early treatment supplement/pharmaceutical studies). https://c19early.org/ - The Federation of State Medical Boards (FSMB). The only resource our team was able to find on this secret board. A video testimonial from an American doctor in New Zealand, Dr Bruce Dooley. https://rumble.com/v1lbjvd-the-dark-truth-of-americas-federation-of-state-medical-boards.html

Dr Robert Malone is an internationally recognised American scientist/physician and the original inventor of mRNA vaccination as a technology, DNA vaccination, and multiple non-viral DNA and RNA/mRNA platform delivery technologies. Dr Malone received his medical degree from the Northwestern Feinberg School of Medicine, completed the Harvard Medical School fellowship as a global clinical research scholar in 2016, and was scientifically trained at the University of California at Davis, the University of California at San Diego, and at the Salk Institute Molecular Biology and Virology laboratories. In this episode we discuss the following: - When and why Dr Malone decided to speak out about his doubts on the safety and efficacy of the COVID-19 vaccines. - Why only gene therapy vaccines were made available in countries like the USA and Australia for the entire year of 2021, when other more traditional vaccines could have been used. - The metaphor of the camel’s nose transhumanism. - The World Economic Forum involvement in government vaccine decision-making. - Dr Fauci, the NIAID, and a financial conflict of interest - The origin of the SARS-COV-2 virus, the furin cleavage site and a super antigen sequence found in the virus. - The new Cell paper from Stanford University, Jan 2022, which shows the vaccine’s mRNA lasting in human lymph nodes for at least 60 days. - Why genotoxicity and reproductive toxicity reports were not done for these gene therapy vaccines. - AIDS post-vaccine. - The metaphor of the Pandora’s box (T cells and latent viruses). - Cancer post-vaccine. - Mass formation psychosis. - The origin of the Omicron variant. - The Unity project. Papers, websites, and books referenced by Dr Malone throughout the interview: - Dr Malone’s website: https://www.rwmalonemd.com/ - Roltgen and colleagues, "Immune imprinting, breadth of variant recognition, and germinal center response in human SARS-CoV-2 infection and vaccination" (which shows that the vaccine’s mRNA is in human lymph nodes at least 60 days after vaccination): https://www.cell.com/cell/fulltext/S0092-8674(22)00076-9 - Book: Professor Mattias Desmet, "The psychology of Totalitarianism" - R W Malone, "Bioethics of Experimental COVID Vaccine Deployment under EUA: It’s time we stop and look at what’s going down." https://trialsitenews.com/bioethics-of-experimental-covid-vaccine-deployment-under-eua-its-time-we-stop-and-look-at-whats-going-down/ Please share this video and subscribe to our channel for more important interviews.

This is a clip from our video interview with Dr Robert Malone. To watch the full interview, visit https://rumble.com/vwwv1h-truth-what-is-truth-an-interview-with-dr-robert-malone.html Please share this video and subscribe to our channel for more important interviews.

Dr Sabine Hazan is a gastroenterologist, she is the first woman ever accepted into the University of Florida as a Clinical Gastroenterology Fellow. Board certified in Gastroenterology, Hepatology, and Internal Medicine, Dr. Hazan has published articles in numerous prestigious medical journals, and won several awards, such as the Best Fellow Scientific Presentation and Dean’s Research Award awarded by University of Florida. She owns a gene sequencing lab and this lab has sequenced the entire SarsCov2 virus from the stools of COVID-19 patients. In this episode we discuss the following: - Dr Hazan’s favourite protocol for treatment of COVID-19. - Did the doctor get COVID-19, and if not, why not? - What is the relationship between the gut microbiome and COVID-19 illness? - Does Ivermectin change the gut microbiome? - Does the COVID-19 vaccination affect the gut microbiome? - Why don’t some people catch COVID-19 despite being exposed? - Censorship of doctors. Papers and video referenced by Dr Hazan throughout the interview: - Hazan and colleagues, "Effectiveness of ivermectin-based multi-drug therapy in severely hypoxic, ambulatory COVID-19 patients" https://www.futuremedicine.com/doi/full/10.2217/fmb-2022-0014 - Hazan and colleagues, "The lost microbes of COVID-19: Bifidobacteria depletion and decreased microbiome diversity are a predictability marker of severe COVID-19, a cross sectional study’’ https://www.medrxiv.org/content/10.1101/2021.09.02.21262832v3?fbclid=IwAR3DG3Z8h4eV7ajOHAbeD4oryUstbE4PKF_3xyig3vdtozmg4CbpdFwtek8 - Video: A Dr. and a Farmer discuss humanity. Dr. Sabine Hazan and Matt Kleopfer (Go to the 47 min mark ) https://www.youtube.com/watch?v=AN7BW1hsQuM Please share this video and subscribe to our channel for more important interviews.

Dr Ryan Cole is a pathologist, board-certified in clinical and anatomic pathology, and is the CEO and Medical Director of Cole Diagnostics. Warner Mendenhall is a lawyer of 24 years and the Principal of the Mendenhall Law Group, in Ohio, USA. He has a lot of experience representing whistle blowers in the past and is part of the legal team representing Brooke Jackson in the current case against Pfizer, regarding fraud in the COVID-19 clinical trial. Craig Kelly is the leader of the United Australia Party (UAP), the party with the largest number of members in Australia. Senator Gerard Rennick is an Australian politician who has been Senator for Queensland since July 2019. He is a member of the Liberal National Party (LNP). Liz Mann was the Organic Development Officer for Australian Consolidated Milk, working with organic dairy farmers in Victoria. She sits on 2 agricultural boards and is the executive officer of 2 industry bodies. She holds a Bachelor of Agricultural Science degree. Liz suffered adverse effects from the Pfizer COVID-19 vaccination. In this episode we discuss the following: - Liz Mann tells her story. She had her first (and only) COVID-19 vaccination on November 23, 2021. Liz was coerced by her employer Australian Consolidated Milk. Liz details the coercion and the communication between herself and her employer. Liz has both heart and neurological damage. - Liz’s Pfizer batch has been revealed as having only 64.5% RNA integrity as per a Freedom of Information (FOI) request that was raised to the TGA (Therapeutics and Goods Administration). Dr Cole comments on the ramifications of truncated RNA in the vaccines and batch purity issues. - Warner Mendenhall is one of the lawyers representing Brooke Jackson in the upcoming Pfizer trial. Warner reads from the Pfizer defence filing to reveal that Pfizer has a “PROTOTYPE agreement” to supply vaccines, not a standard federal procurement contract. - Pfizer have said “You are claiming we violated all these regulations but we don’t have to follow them as it is a prototype." - Warner relayed the following information from a manufacturing whistle blower from a Pfizer manufacturing plant. The soup story. There is an issue with manufacturing the mRNA vaccine on scale. In the big Vats, the LNP (fat) separates and rises to the top. It cannot be stirred aggressively, or the mRNA will break. Hence there is not a consistent product in the vials, vials from the bottem contain little or no mRNA, and vials from the top contain far too much. They are issuing an adulterated product. - Senator Rennick had produced information from an FOI raised by one of his constituents (FOI 295). It states that the TGA does not set integrity and purity requirements for mRNA vaccines. The sponsor does. - Senator Rennick also confirmed that many Australians had approached him and logged their information on his webpage regarding coercion for a second shot after injury from the first, like Liz Mann. - Dr Ryan Cole discusses the danger of the spike protein and the LNP, and recommends that this platform for vaccines should be ceased indefinitely. - Craig Kelly discusses the legislation he tried to put through to ban the vaccine mandates. - Craig Kelly discusses a new manufacturing plant proposed for Australia. Please share this video and subscribe to our channel RefugeOfSinners on Rumble (https://rumble.com/user/RefugeOfSinners) for more important interviews.