@JohnBoweActor - John Bowe
Fellow citizens of the UK, some of this may ring bells.
@JohnBoweActor - John Bowe
FOR IMMEDIATE RELEASE 10 OCT 2023 WORLD COUNCIL FOR HEALTH EXPERT PANEL FINDS CANCER PROMOTING DNA CONTAMINATION IN COVID-19 VACCINES International expert panel concludes that Covid vaccines are contaminated with foreign DNA and that SV40, a cancer-promoting genetic sequence has been found in the vaccines Bath, U.K. – The World Council for Health, in collaboration with expert advisers, is dedicated to providing the public with accurate and reliable information to promote health and well-being. In light of recent concerns regarding bacterial DNA and genetic sequences in mRNA vaccines, the World Council for Health organized an Urgent Expert Hearing on this critical topic on Monday 9th October. The hearing took place virtually and addressed the implications of these findings for all people of the world. The following internationally renowned immunologists, geneticists, specialist physicians and research scientists shared their findings with the audience: •Kevin McKernan (USA) •Dr Janci Lindsay (USA) •Prof Sucharit Bhakdi (Germany) •Assoc Prof Byram Bridle (Canada) •Dr Peter McCullough (USA) •Prof Brigitte König (Germany) •Dr Jessica Rose (Canada) •Prof Alexandra Henrion-Caude (France) •Attorney Katie Ashby-Koppens (Australia) shared the legal implications of the deployment of unregulated GMO products as vaccines Summary of Findings: 1Bacterial DNA (plasmids) has been found in mRNA vaccine vials. 2A cancer-promoting genetic sequence—SV40—has been found in the Covid-19 vaccines. This was not present in the vials used for the approval studies but has been found in all vials of the BioNTech vials disseminated for public use. 3These discoveries have been confirmed in several independent laboratories worldwide. 4The discovery was originally made in April 2023 by Kevin McKernan at which point regulatory bodies were contacted. No official reply has been received. 5Multiple mechanisms exist in which this genetic information might be integrated into the human genome. 6This DNA could instruct our bodies to produce mRNA and foreign proteins for an unknown period with potential implications for subsequent generations. 7There is no constructive purpose identified for the undeclared SV40 promotor sequence, which in addition to its cancer risk, enhances the capacity to incorporate the other foreign genetic material into the recipients’ own chromosomes potentially rendering them (and possibly even their offspring) permanently genetically modified. 8There are multiple completely undeclared genetic sequences in both Moderna and Pfizer vials with the SV40 sequence found only in the Pfizer vials. However, latent SV40 infections in a significant portion of the population could present the same SV40 risk to Moderna recipients. 9Even in the absence of chromosomal integration, the DNA plasmids could generate mRNA for the spike protein toxin and other harmful proteins for prolonged and unpredictable periods of time. 10Integration of foreign DNA into the human genome disrupts existing natural genetic sequences; this carries further risk of disease including cancer. 11The Covid-19 vaccines qualify as GMO (genetically modified organism) products, which require approval in addition to that required for older, more traditional vaccines. 12Informed consent for these products is impossible as the risks of the products have never been formally and transparently assessed by regulators and are not fully known. Independent assessment of the emerging and available evidence is that these products are extremely dangerous with implications for disease, death, transmission and inheritance. 13An immediate moratorium on these novel genetic “vaccines” was demanded by the expert panelists.
@JohnBoweActor - John Bowe
BREAKING--Pfizer XBB.1.5 Monovalent Vaccine Tested in 20 Mice, No Control Group, and No Humans Emergency Authorization Granted without Emergency or Human Data PETER MCCULLOUGH, MD SEP 13 By Peter A. McCullough, MD, MPH At this point, the American public and scientific community is flabbergasted at the complete regulatory malfeasance committed by US FDA VRBPAC and CDC panelists. As of September 12, 2023, the prior bivalent (original Wuhan /BA4/BA5 mRNA Code) has been retired and the new XBB.1.5 monovalent vaccines have been emergency use authorized. From the Pfizer core slides released today, there was a single experiment with 10 mice assigned to the prior BA4/BA5 bivalent and 10 assigned to the new XBB.1.5 monovalent vaccine. They were injected twice, 21 days apart. The new booster was authorized for a single 30 mcg shot in humans.  The pseudoviral antibody responses were greater for the new vaccine against the outgoing XBB.1.5 (3.1% of strains as of 9/2/23) and the incoming EG.5 (Eris) strain at 21.5%, but no information was given about and FL.1.5.1 which is growing at 14.5% in the US population.  There were no human studies presented in the core slides by Pfizer. It impossible to predict what would happen with a single human injection. Their last slide was a single ongoing clinical study of the new vaccine. There are two age groups, no randomization and no control group. There is zero chance to assess human safety or efficacy of the XBB.1.5 vaccine in sponsored studies.  The only thing that will stop ongoing scientific misconduct and regulatory malfeasance is public outrage and booster refusal. The vaccine companies are hauling in record profits, have not analyzed safety nor have they shown any interest in safer more effective products for testing in large-scale randomized double-blind placebo controlled trials. The Bio-Pharmaceutical Complex is completely off the rails! Coming next will be vaccines developed from computer generated mRNA genetic code with mathematical modeling of antibody response and no mice or human subjects at all.
@JohnBoweActor - John Bowe
Pay close attention to what this great man says………… @drcole12 I salute you.
@JohnBoweActor - John Bowe
Just received this from Dr Pierre Kory…… John, As I was scrolling through articles the other day, I stumbled upon this headline: CDC Launches Effort to Bolster Hospital Sepsis Programs. Wary, but a tad hopeful, I clicked on the link to read more about it. After a few sentences, it was clear that our ‘bastion of public health’ was up to its old tricks again. Here’s what they recommend: 1Antibiotics 2Bureaucracy, and 3More Bureaucracy Oh, and SHOCKER . . . don’t forget to get your COVID, Flu, and RSV vaccines to prevent sepsis. Perhaps by now I shouldn’t be surprised. Heaven forbid should our government actually suggest treatments that work. The trouble is, this is no laughing matter. Nearly 1.7 million people get sepsis every year, and over 350,000 of those patients die. One in three patients who die in a hospital have had sepsis during their time there. These are staggering statistics and - just as with COVID - it wouldn’t have to be this way. Because sepsis is treatable. As many of you know, our own Dr. Paul Marik witnessed the ineffectiveness of the ‘standard of care’ sepsis protocol during his time in the ICU and knew there must be a better way. He had read Dr. Fowler's research on using high dose Vitamin C to treat the illness, tried it with a patient who was near death in 2016, and the patient survived! From there, Paul developed his genius protocol incorporating intravenous vitamin C combined with thiamine (vitamin B) and corticosteroids. After treating multiple patients successfully with this combination, he was lauded by the nurses and administration at his hospital . . . until they got the memo from top brass, which prompted everyone to change their tune. Sigh . . . Disrupt healthcare with us Regardless, his research was highly credible, ground-breaking, and was eventually published in the well-regarded medical journal CHEST. Even after a recent attack by a social media influencer (they seem to come out of the woodwork these days. . . ), his paper has been defended and acknowledged by the journal’s editors for its scientific validity. In short, this protocol works!! A side note, the fight for its recognition and effectiveness is also how Paul and I came together as the dissident, disruptive rebel-rousers you know (and hopefully love?) today. But that’s a story for another time. As evidenced by all that they did (and didn’t do) during COVID, and this latest ridiculousness around “bolstering sepsis programs,” our public health agencies are proving again and again that they could care less about your health and, in many ways, are incentivized to keep you sick. The FLCCC, on the other hand, is dedicated and morally compelled to provide you with alternative options so that you and your loved ones can get well. Today, I want to share with you our most updated Sepsis Protocol, should you or anyone you know need it. We are offering this FREE OF CHARGE on our website, as we do with all of our research and protocols. Take this, print it off, and share it far and wide - help us get the word out that sepsis, just like COVID, is indeed treatable. John, it’s long past time to stop the needless deaths due to inept hospital “standards of care” - please join us as we fight an archaic, corrupt system and make a gift today to help us advance solution-based, patient-focused medicine. Your gift will - quite literally - help save lives. With your support, we can pursue and expand upon this critical research, reach people across the world, and continue to be a positive force for change in the midst of this bureaucratic catastrophe. As you know, with the FLCCC, you can count on medical treatments and advice you can trust, free of ANY conflicts of interest. We are certainly the disruptors, and we wear that badge with honor. Thank you for shaking things up with us. Yours in truth and health, Pierre Kory, MD, MPA