In the previous article I asked if anyone had experience evaluating western blots. This was because, last week, while investigating one of the central questions we’ve had about the vaccines, we inadvertently discovered something highly suggestive of fraud.
Fraud is a huge allegation to put forward, so since that time we did our best to vet the discovery and sent it out to independent parties who could validate it prior to publishing. Based on the feedback we have received since publishing this, there is a chance one of my key allegations is false (that the image being a digital straight line means it was not representative of the actual proteins present) as there was an additional approach to evaluating this we were not aware of at the time of publication.
I still believe the central allegation (that the vaccines do not contain what was advertised) holds true and is critically important to understand. At this point in time we do not presently have the information to determine if the numerous suspicious characteristics we specifically identified in Pfizer’s western blots could be explained by anything besides fraud and eagerly invite any clarifications on this issue.
Legal Priorities
One of the things that is less appreciated about governance is that governments will never have the resources to address every single problem that arises in their territory. Because of this, governments inevitably prioritize addressing problems which would otherwise cause them to lose money, and will prioritize protecting the (typically financial) interests of the upper class who support government officials (e.g., by paying for their election).
This has lead to the curious phenomena whereby there are much harsher penalties for institutional level fraud then there are for an institution harming members of the general public. For example, as I have tried to show throughout this Substack, pharmaceutical companies frequently commit egregious harm against consumers and clinical trial participants, but in spite of this, most of our institutions will refuse to prosecute them for this conduct. Conversely, one of my friends who is a paralegal in the industry has told me that pharmaceutical companies have to be honest with their investors, or they can and will be sued for financial fraud. For this reason, you can typically get the most accurate information on their products by reviewing what pharmaceutical companies share with their investors.
Similarly, although by all reasonable standards, Pfizer and Moderna should be criminally convicted for allowing such a dangerous vaccine on the market (they clearly knew the vaccines had to be dangerous), nothing has been done. However, Brook Jackson is currently pushing through a whistleblower lawsuit against Pfizer which makes the case that Pfizer conducted their clinical trials in a fraudulent manner, and by extension, committed fraud. The sale of the vaccines to the US government was predicated upon their clinical trial data and thus if that data was fraudulent, Pfizer’s sales constitute fraud.
Because fraud has much greater standing in our legal system than harming the general public, Brook’s lawsuit is critically important, and if it succeeds in proving fraud on Pfizer’s end, can collapse this entire vaccination campaign. Likewise, Brook has an even stronger case if a smoking gun were to be present which:
1) Showed that Pfizer beyond a shadow of a doubt intentionally committed fraud.
2) This fraud directly undermined the entire basis for their product.
So understandably, we wanted to make sure our allegations were correct before moving forward.
Why Are Only Some People Getting Ill From The Vaccines?
One of the early observations with the COVID-19 vaccines is that the response to them was much more variable than what we typically associated with a pharmaceutical product. Many felt awful for a prolonged period, some people had severe reactions, far too many died, butmany others had no reaction at all. This suggested to me that at least one of the following was true (none of these are mutually exclusive):
There are certain predisposing factors to having severe reactions to the vaccine.
The previous article detailed one apparent culprit: the inability to properly form antibodies that neutralize the otherwise toxic spike protein. There are also many other potential culprits which provide numerous invaluable insights about human physiology and illness (and will be discussed in the next article).
Hot lots (lots that are significantly more toxic) are being deliberately tested on the population. The argument for this was as follows:
1) I and readers here have observed small clusters of individuals who appeared to have been vaccinated at the same time or location and all died not long after vaccination. Given that sudden death, even after COVID-19 vaccination, is a rare occurrence, I do not believe this can be mathematically explained unless the lot those unfortunate individuals received (or at least the individual vial they both received) was hot.
2) A major challenge with the mRNA technology was establishing the appropriate dose. Every single drug needs to be given at a certain concentration to be effective, and has a concentration where it becomes toxic. The difference between these two is known as the therapeutic window, and safe drugs have wide therapeutic windows, while dangerous drugs have narrow therapeutic windows and have to be given under supervision. One of the major stumbling blocks for the mRNA technology prior to COVID-19 is that by the time enough of it was given to cells for the gene product to be produced, cellular toxicity also occurred. For this reason, I felt that there was a genuine need to find a way to determine the appropriate dosing of the mRNA vaccines and due to the time constraints being worked with and difficulty of the problem, this likely would not be possible until after they entered the global market.
3) Approximately 30 years ago, a forced vaccination campaign with an experimental anthrax vaccine was conducted on the US military. I have written about this both because it was an unknown tragedy, but also because I believe it was the beta test for what happened with the COVID-19 vaccines. When it was all said and done, over 100,000 soldiers were significantly injured by something (which was almost certainly the vaccine). At the time, numerous investigations were launched (including congressional hearings) to find out what happened with these vaccines, although since that time most of what transpired has mostly been forgotten (as the result of this scandal was the military being forbidden from forcing experimental vaccines onto our servicemen, yet this is exactly what happened with the COVID-19 vaccines). Fortunately, this subject was recently revisited by a sitting member of congress.
One (but not the only) compelling theory to explain what happened was that the Department of Health and Human Services (HHS) needed to develop an oil-based adjuvant in order to make many of the vaccines they had in the pipeline viable. In turn, our soldiers were experimented upon in order to determine the appropriate dosing of the new adjuvant. The points of support for this theory were:
•Many of those involved in this operation (and never faced consequences for their conduct) decades later also played key roles in Operation Warp Speed.
•The entire operation was run in a very suspicious fashion and the vaccine that the soldiers received was only labeled as “vaccine A” on their cards but did not appear in their medical records.
•An antibody test to squalene was developed after one physician realized many of the symptoms that the Gulf War veterans were experiencing could have been caused by an injection of squalene, which created auto-immunity to it (later a doctor who received an experimental herpes vaccine utilizing a squalene adjuvant came forward, and testified that from that he also developed the symptoms characteristic of Gulf War Syndrome). This antibody test was positive, and many of the veterans who had severe issues after the vaccination were positive. To further support this link, servicemen who have no choice except to vaccinate, volunteered to provide their blood before and after vaccination, and it was demonstrated that the vaccination caused the development of antibodies to squalene.
•After the colonel of an Air Force Base suspended the vaccine because multiple severe injuries happened to his servicemen immediately following vaccination, the Pentagon sent high ranking officials to reinstate the program. At the town hall they hosted, they initially denied that a squalene-based adjuvant was being used, and then later admitted that adjuvant was being looked at but would never be used in the anthrax vaccines.
•Later testing of the anthrax vaccine lots suspected to be hot lots (performed by the FDA) found that they contained squalene, and that the concentrations present precisely matched what would be expected in a dose response study to evaluate the effect of the adjuvant on humans. Although the geometrical increase in dose concentrations found almost certainly could not have happened without them being intentional, this point of evidence is also disputed because of just how low the concentrations were.
•At the time this happened, one of the Airforce captains who tried to stop the horrific injuries he observed in his fellow servicemen from continuing remarked: ““I want you to burn these two letters and two numbers into your consciousness (MF59) so you will remember them because squalene will next be used in civilian vaccines.”
Years later, MF59 entered the market and is now used in numerous vaccines the general public receives as an adjuvant (squalene was also an adjuvant for some of the COVID-19 vaccine candidates that ultimately did not win the vaccine race).
This progression through a rocky “experimental” phase is somewhat similar to what happened with the hCG vaccines. These vaccines were the result of decades of research into how vaccination could be used to sterilize people in the third world (hCG, a hormone essential to pregnancy was eventually identified as the optimal target for sterilization through immunization). Initially the hCG vaccines were deployed covertly for forced “tetanus“ vaccination campaigns targeted to women of childbearing age. After what was happening was discovered, the authorities denied hCG could be present, but enough outcry met the campaigns that they were nonetheless suspended.
Years later, after Gates began funding the WHO, and shifting their priority to vaccination, the “tetanus” campaign was re-introduced to Kenya, and this time (knowing what had happened there before) local doctors were able to obtain evidence demonstrating that hCG was in fact in the suspect vaccines. Now, going further down the road, rather than it being a conspiracy theory, you can actually find numerous references to sterilizing vaccines if you search for “immunocontraception” on Pubmed.
4) ) In addition to making a very strong case that there were “hot vaccine lots,” Craig Paardekooper’s team has also discovered many concerning patterns within the toxic lots. For example, they observed in Pfizer’s case, the toxicity of their vaccines directly correlated to their sequential lot numbers. This is highly suggestive that a dose response trial was being conducted and as sequentially higher doses of the drug are coded in a simple manner researchers can understand.
5) A few of my colleagues who are excellent diagnosticians have told me that they are relatively certain some (but not all) of their “vaccinated” patients had received a saline placebo.
Assuming you do not adopt a nefarious interpretation (e.g., depopulation) the primary motivation behind the vaccines was almost certainly to make money. This was either by:
•Getting the mRNA technology to the market (as it represented an enormous market I would guess is in the trillions for an industry that is presently struggling to find new products as it is getting harder and harder to identify new drug candidates within the current drug development model).
Or
•Being fast enough to make it to the finish line and land a lucrative government contract for the Operation Warp Speed vaccines.
The impetus behind Fauci’s vision for mRNA vaccines was that it always takes a significant amount of time to produce the antigens that all vaccines require, especially in large quantities. This issue is particularly evident with the annual influenza vaccinations, as production of its antigen takes time and has to start well before the strain that will circulate for that year is known. As a result, regardless of the modeling used, the strain that is ultimately picked for the vaccine is frequently the wrong one.
The promise of the mRNA technology was that once the genetic sequence for the antigen in question was known, it would be possible to plug it into the mRNA platform and rapidly produce the vaccines. This is essentially what Pfizer and Moderna attempted to do for COVID-19.
The problem with this approach was that the technology to pull it off was still not there. One of the largest stumbling blocks encountered in biotech is moving from having a viable prototype you can produce in the lab to being able to manufacture it on a large scale. This is always extremely challenging to do, and the idea that it could be done properly with a brand new technology with numerous major obstacles, in a fraction of the time frame that would be required, was quite frankly, delusional.
In the previous article I asked if anyone had experience evaluating western blots. This was because, last week, while investigating one of the central questions we’ve had about the vaccines, we inadvertently discovered something highly suggestive of fraud.