June 12, 2022
Dr. Ryan Cole: “There are studies by Dr. [Resia] Pretorius out of South Africa that show that you can take the spike protein alone, without platelets in the plasma, and that spike protein alone causes the proteins in our blood to clump. That spike protein is thrombogenic; it causes clots, and it causes a lot of clots.”
July 13, 2022
The modified spike protein is dangerous and for very specific reasons.
Hereâs a vial of these raw clots, washed [free] of blood and preserved, before staining. These structures that were evacuated from inside blood vessels during embalming procedures within hours of death.
Unlike normal clots which are gelatinous, almost jelly-like, these so-called âclotsâ contain extremely large, complex, repeating structural elements (all shown in link below) that are clearly being constructed in the blood of the victims who died from these clots.
I believe these structures may very well explain why so many seemingly healthy adults are suddenly dying.
The pathologist doesnât know what these are. The embalmers donât know what these are. But they know what they are not.
So, now us non-embalmer laymen can rest assured that these strange white fibrous proteinacious structures are not blood clots. The structures did, however, obstruct the flow of blood in the arteries of these individuals and likely is what killed them.
In conclusion, they are not âbloodâ clots. They are structures in the blood. They are âstructural clotsâ or âfibrous clotsâ that are extremely large and are being constructed inside the body over time.
My grave concern is that every person who has been injected with mRNA instructions may be constructing these fibrous structures inside their bodies at this very minute, and that itâs only a matter of time before they block major arteries or cause heart attacks, strokes or other acute causes of âSudden Adult Death Syndromeâ (SADS).
PLEASE CLICK THIS LINK FOR DETAILS:
https://jessicar.substack.com/p/lets-tag-team-this-until-everybody?utm_source=email&s=r
Dr. Jessica Rose is a Canadian researcher with a Bachelor’s Degree in Applied Mathematics and a Master’s degree in Immunology from Memorial University of Newfoundland. She also holds a PhD in Computational Biology from Bar Ilan University and 2 Post Doctoral degrees: one in Molecular Biology from the Hebrew University of Jerusalem and one in Biochemistry from the Technion Institute of Technology. She was also accepted for a 2-month program as a senior researcher at the Weizmann Institute prior to completion of her latest post doctoral degree at the Technion. Her more recent research efforts are aimed at descriptive analysis of the Vaccine Adverse Event Reporting System (VAERS) data in efforts to make this data accessible to the public.
June 6, 2022
Freddie Sayers sits down to discuss the pandemic response with biologist Bret Weinstein. Before the pandemic, evolutionary biologist and former Evergreen professor Bret Weinstein was lauded by both sides of the political divide for his insights into the crisis on American campuses. As a member of the so-called ‘intellectual dark web’, Weinstein was expanding his audience and being profiled by legacy media like the New York Times. Then the pandemic began and his heterodox perspective suddenly fell out of favour, even with many of his erstwhile allies. Advocating for alternative treatments for Covid, questioning the efficacy of the global vaccine programme and challenging narratives of the pandemic came at a cost. Without warning, the Dark Horse podcast was demonetised on YouTube and Weinstein was forced to split from the views of his former friends and supporters. So, how can we seek truth in such divided times? Freddie Sayers invited Bret into the UnHerd studio in London to try to understand what his views really are.
Read the supporting article: https://unherd.com/thepost/bret-weins…
Listen to the podcast version: https://shows.acast.com/lockdowntv-wi…
// TIMECODES // 00:00 – 01:31 – Introduction 01:31 – 04:43 – What have we learnt about the state of the world, post-pandemic? 04:43 – 06:26 – What mistakes were made? 06:26 – 12:31 – Is this pandemic response we experienced, going to become the norm? 12:31 – 14:34 – What does Bret see as the disaster in the pandemic response? 14:34 – 17:50 – Was it worthwhile vaccinating younger people? 17:50 – 22:22 – Were there darker forces at play when it came to the vaccination programme? 22:22 – 24:48 – Bret discusses the âBetter Way conferenceâ he attended 24:48 – 28:33 – What is the worst case scenario behind the pandemic response? 28:33 – 31:14 – In a few decades time, will we see a generation with a decreased lifespan? 31:14 – 39:11 – Bretâs opinion on The Pandemic Treaty 39:11 – 43:30 – What is down the road for us? Will there be a new pandemic? 43:30 – 45:36 – Whatâs in store for Bret? 45:36 – 47:29 – Is the worst still yet to come? 47:29 – 48:11 – Conclusion
November 6, 2010 (yet still applies)
June 9, 2022
2021
Autoimmune diseases (ADs) could occur due to infectious diseases and vaccination programs. Since millions of people are expected to be infected with SARS-CoV-2 and vaccinated against it, autoimmune consequences seem inevitable. Therefore, we have investigated the whole proteome of the SARS-CoV-2 for its ability to trigger ADs. In this regard, the entire proteome of the SARS-CoV-2 was chopped into more than 48000 peptides. The produced peptides were searched against the entire human proteome to find shared peptides with similar experimentally confirmed T-cell and B-cell epitopes. The obtained peptides were checked for their ability to bind to HLA molecules. The possible population coverage was calculated for the most potent peptides. The obtained results indicated that the SARS-CoV-2 and human proteomes share 23 peptides originated from ORF1ab polyprotein, nonstructural protein NS7a, Surface glycoprotein, and Envelope protein of SARS-CoV-2. Among these peptides, 21 peptides had experimentally confirmed equivalent epitopes. Amongst, only nine peptides were predicted to bind to HLAs with known global allele frequency data, and three peptides were able to bind to experimentally confirmed HLAs of equivalent epitopes. Given the HLAs which have already been reported to be associated with ADs, the ESGLKTIL, RYPANSIV, NVAITRAK, and RRARSVAS were determined to be the most harmful peptides of the SARS-CoV-2 proteome. It would be expected that the COVID-19 pandemic and the vaccination against this pathogen could significantly increase the ADs incidences, especially in populations harboring HLA-B*08:01, HLA-A*024:02, HLA-A*11:01 and HLA-B*27:05. The Southeast Asia, East Asia, and Oceania are at higher risk of AD development.
June 10, 2022
More video here:
June 7, 2022
Dr. Joel Hirschhorn, MD pulls no punches going after the political & bureaucratic attacks on medicine. Excess deaths in heavily vaccinated Taiwan & Australia. And, what we’re learning about treating long term effects of jab.
June 5, 2022
Dr. Mike Yeadon: “The elapsed time taken to get an adequate amount of safety data is always longer than the feasible length of any pandemic in history. In other words, a new vaccine is always, let me say it again, always, Mr. Gates, the wrong answer. It will always take you longer to do a responsible job of creating and testing a novel vaccine than the length of the pandemic. And if you take less time, it means you do not have an appropriate amount of safety data and therefore it’s reckless to go and vaccinate the whole population.”