STORY AT-A-GLANCE
- The reason health officials don’t want individual vaccine vials examined by independent scientists is because the vials are all different — and the mRNA in the shots is not intact
- For an effective mRNA product, the mRNA integrity needs to be 100%, meaning all the RNA must be intact. Considering how ineffective the jabs are, it seems fair to question whether lack of mRNA integrity might be to blame
- Fragmented RNA could potentially also be hazardous to health by generating incomplete spike proteins. While we do not know if incomplete spike proteins are dangerous, it’s possible they might contribute to cellular stress
- The “bad batch” phenomenon may also be indicative of quality problems. Independent investigations have revealed that some lots of the shots are associated with very severe side effects and death, whereas other lots have very few or no adverse events associated with their use
- However, the fact that “hot” lots are being released in a coordinated fashion suggests vaccine makers may in fact be doing intentional lethal-dose testing on the public, and that these “bad batches” are not merely the result of intermittently poor manufacturing
A 14-minute video (above) that has been overlooked for nearly two years has now resurfaced, exposing stunning information about the COVID-19 jabs and why health officials don’t want individual vaccine vials examined by independent scientists.
The reason, it turns out, is because the vials are all different — and the mRNA in the shots “is not intact.” Both of these pose potentially serious problems. In an August 31, 2022, Substack article, Steve Kirsch explains:1
“Even if you are getting 100% intact mRNA which would be really rare, you’re still not getting anything that resembles the virus. So the efficacy as far as PROTECTING you will be next to nothing.
However, what it will do very effectively, if you got reasonably intact mRNA, is to cause you significant harm. You are playing a game of chance with your immune system and what is in the bottle.”
The video notes that members of the European Parliament were only allowed to read the contracts with the drug makers after they’d been heavily redacted. Why the heavy-handed secrecy, even toward legislators?
Leaked Documents Reveal Serious Quality Issues
The finding that the mRNA in the shots was of questionable quality was revealed in a BMJ feature investigation article2 published in March 2021. As explained by the author, journalist Serena Tinari, cyber attackers retrieved more than 40 megabytes of Pfizer COVID jab data from the European Medicines Agency (EMA) in December 2020.
The hacked data was subsequently sent to journalists and academics worldwide. It was also published on the dark web. Some of the documents show European regulators had significant concerns over the lack of intact mRNA in the commercial batches sampled.
Compared to the clinical batches, i.e., the shots used in the clinical trial, 55% to 78% of the commercial shots had “a significant difference in % RNA integrity/truncated species.”
In one email, dated November 23, 2020, a high-ranking EMA official noted that the commercial batches failed to meet expected specifications, and that the implications of this RNA integrity loss were unclear. In response to the findings, the EMA sent a list of questions and concerns to Pfizer.
While we do not know if and how the EMA’s concerns were actually addressed and corrected, the EMA authorized Pfizer’s COVID jab December 21, 2020. According to its public assessment report, “the quality of this medicinal product, submitted in the emergency context of the current (COVID-19) pandemic, is considered to be sufficiently consistent and acceptable.”
Similarly, Health Canada told The BMJ that “changes were made in their processes to ensure that the integrity was improved and brought in line with what was seen for clinical trial batches.” The EMA further tried to deflect concern by claiming some of the leaked documents had been doctored. As reported by The BMJ:3
“EMA says the leaked information was partially doctored, explaining in a statement that ‘whilst individual emails are authentic, data from different users were selected and aggregated, screenshots from multiple folders and mailboxes have been created, and additional titles were added by the perpetrators.’”
Intact mRNA Is Essential to Its Effectiveness
Curiously, when The BMJ asked Pfizer, Moderna, CureVac and several regulators to specify the percentage of mRNA integrity considered acceptable, none replied with specifics.
According to the British Medicines and Healthcare Products Regulatory Agency, the FDA and Health Canada, the specification limit on RNA integrity is “commercially confidential.” What we do know — and the EMA has acknowledged — is that intact mRNA is essential for efficacy. As noted by The BMJ:4
“… the documents offer the broader medical community a chance to reflect on the complexities of quality assurance for novel mRNA vaccines, which include everything from the quantification and integrity of mRNA and carrier lipids to measuring the distribution of particle sizes and encapsulation efficiency.
Of particular concern is RNA instability, one of the most important variables relevant to all mRNA vaccines that has thus far received scant attention in the clinical community …
RNA instability is one of the biggest hurdles for researchers developing nucleic acid based vaccines. It is the primary reason for the technology’s stringent cold chain requirements and has been addressed by encapsulating the mRNA in lipid nanoparticles.
‘The complete, intact mRNA molecule is essential to its potency as a vaccine,’ professor of biopharmaceutics Daan J.A. Crommelin and colleagues wrote in a review article in The Journal of Pharmaceutical Sciences late last year.
‘Even a minor degradation reaction, anywhere along a mRNA strand, can severely slow or stop proper translation performance of that strand and thus result in the incomplete expression of the target antigen.’”
For an effective product, mRNA integrity needs to be 100%. Considering how ineffective the jabs are, it seems fair to question whether lack of mRNA integrity might be to blame. We also do not know whether nonintact mRNA might be harmful.
As noted by Kirsch,5 “Unstable mRNA means the spike protein … cold collapse, making the whole process useless to support immunity, but still dangerous in terms of damage to cells. So, you get all the risk and no benefit.”
While our public health agencies claim fragmented RNA poses no health risk, just how do they know that? The leaked documents revealed they specifically did not have an answer to that question, and no research into the matter has been published, that I’m aware of.
Fragmented RNA May Produce Incomplete Spike Proteins
In May 2021, Stephanie Seneff, Ph.D., a senior research scientist at MIT for over five decades, published an excellent paper6 in which she highlighted several potential dangers of the COVID jabs, including the unknown hazard of injecting fragmented RNA. That same month, I interviewed her about her concerns. You can find that interview in “COVID Vaccines May Bring Avalanche of Neurological Disease.” In her paper, Seneff noted:7
“The EMA Public Assessment Report … describes in detail a review of the [Pfizer] manufacturing process … One concerning revelation is the presence of ‘fragmented species’ of RNA in the injection solution. These are RNA fragments resulting from early termination of the process of transcription from the DNA template.
These fragments, if translated by the cell following injection, would generate incomplete spike proteins, again resulting in altered and unpredictable three-dimensional structure and a physiological impact that is at best neutral and at worst detrimental to cellular functioning.
There were considerably more of these fragmented forms of RNA found in the commercially manufactured products than in the products used in clinical trials. The latter were produced via a much more tightly controlled manufacturing process …
While we are not asserting that non-spike proteins generated from fragmented RNA would be misfolded or otherwise pathological, we believe they would at least contribute to the cellular stress that promotes prion-associated conformational changes in the spike protein that is present.”
Kirsch points out that the EMA also expressed concern over visible particles in the vials, which The BMJ did not follow up on. “Is it still a problem?” Kirsch asks. That’s a good question, and the answer is probably yes.
But even worse is that we have absolutely no idea what these incomplete spike proteins are doing, none, zero, nada. It has never been directly examined. For that matter efforts to evaluate, and complications of the jab, have been consciously suppressed as have following simple metrics such as increases in all-cause mortality.
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Deaths Dismissed and Side Effects Misclassified
The leaked EMA documents also showed that Pfizer dismissed all deaths in its trial as “unrelated to the vaccine,” even though no proper investigation was ever conducted. We now have additional evidence of this — just like the court-ordered FOIA documents showed what Pfizer did in their U.S. trials. At least they are consistent in implementing their fraud.
As reported by Children’s Health Defense (CHD) back in June 2022, Freedom of Information Act (FOIA) documents, released by court-order, reveal Pfizer classified nearly all severe reactions in its trials as unrelated to the shot, even in cases where the health problems in question are extremely difficult to dismiss as anything other than a direct effect of the shot:8
“The latest release by the U.S. Food and Drug Administration (FDA) of Pfizer-BioNTech COVID-19 vaccine documents9 reveals numerous instances of participants who sustained severe adverse events during Phase 3 trials. Some of these participants withdrew from the trials, some were dropped and some died …
The CRFs [case report forms] included in this month’s documents contain often vague explanations of the specific symptoms experienced by the trial participants. They also reveal a trend of classifying almost all adverse events — and in particular severe adverse events (SAEs) — as being ‘not related’ to the vaccine …
The many serious adverse events — and several deaths — recorded during the Phase 3 trials are also apparent in a separate, massive document10 exceeding 2,500 pages, cataloging such adverse events.
This document lists a wide range of adverse events suffered by trial participants classified as toxicity level 4 — the highest and most serious such level. However, not one of the level 4 (most severe) adverse events listed in this particular document is classified as being related to the vaccination.”
As just one example,11 a teenage girl got the shot September 11, 2020, and in mid-November 2020 was diagnosed with right lower extremity deep vein thrombosis, which we now know is a potential side effect of the jab. According to the CFR, her condition was due to a bone fracture that occurred before the date of her injection — a determination that seems questionable at best.
What’s the Cause Behind the ‘Bad Batch’ Phenomenon?
The “bad batch” phenomenon may also be indicative of quality problems. Independent investigations have revealed that some lots of the shots are associated with very severe side effects and death, whereas other lots have very few or no adverse events associated with their use.
According to howbadismybatch.com, a site that matches up vaccine lot codes with reports in the VAERS system, approximately 5% of the lots are responsible for 90% of all adverse reactions. Some of these batches have 50 times the number of deaths and disabilities associated with them, compared to other lots.12
Another website that basically does the same thing is TheEagle’s VAERS Dashboard. A video explaining how to use the dashboard can be found on Bitchute.13
However, an even deeper dive into this data suggests random quality issues are not the problem. In the video above, Reiner Fuellmich, cofounder of the German Corona Investigative Committee, and Dr. Wolfgang Wodarg, a former member of the German parliament, discuss this “smoking gun” evidence.
According to Fuellmich and Wodarg, the lot-dependent data suggests vaccine makers may be conducting secret experiments within the larger public trial. In other words, they appear to be doing lethal-dose testing on the public. The tipoff that these “hot” batches are not caused by intermittent poor manufacturing is the fact that they’re being released in a coordinated fashion.
Wodarg argues that the evidence for this is very clear from the data. Basically, the vaccine manufacturers are coordinating their lethal-dose experiments so that they’re not all releasing their most toxic lots at the same time, or in the same areas. This avoids detection through clustering.
New Boosters Will Not Undergo Additional Testing
Considering the multitude of open questions surrounding the safety of the original COVID shots, the fact that new, reformulated boosters will not require any additional testing whatsoever is beyond disturbing.
In the “Friday Roundtable” video above, Dr. Meryl Nass, Toby Rogers, Ph.D., Aimee Villella McBride, Polly Tommey and Brian Hooker, Ph.D., discuss the FDA’s decision to allow vaccine makers to reformulate their COVID shots without additional testing, in perpetuity.
As noted by Rogers, Pfizer’s bivalent booster against Omicron variants BA.4 and BA.5 was tested on a total of eight mice, and only to check antibody levels. Moderna also used mice to ascertain antibody responses, but have not disclosed the number of mice used.
That’s the extent to which these shots were tested. The original COVID jabs are the most dangerous drugs ever released to the public, and these newer boosters may turn out to be even worse.
As explained by Rogers, the shots “imprint” your immune system to respond only to the antigen in the shot, while simultaneously impairing your immune system so that it’s less capable of protecting you against other pathogens. Another term for this process is “original antigenic sin.” It essentially explains why those are jabbed are getting infected and sicker than those who avoided the jabs.
Rogers predicts we’ll be faced with a winter of severe illness and death among those who have gotten the jabs. All the rest of us can do is stand back, avoid the shots at all cost and “let the mainstream system self-destruct.” Hopefully, he’s correct in his other prediction, which is that the vast majority of Americans will reject these boosters.
- 1, 5 Steve Kirsch Substack August 31, 2022
- 2, 3, 4 BMJ March 10, 2021; 372: n627
- 6, 7 International Journal of Vaccine Theory, Practice and Research May 10, 2021; 2(1): 402-444
- 8, 11 The Defender June 22, 2022
- 9 PHMPT.org Pfizer documents
- 10 PHMPT.org Adverse events legend
- 12 Robert Malone Substack January 13, 2022
- 13 Bitchute December 29, 2021
Five Things New “Preppers” Forget When Getting Ready for Bad Times Ahead
The preparedness community is growing faster than it has in decades. Even during peak times such as Y2K, the economic downturn of 2008, and Covid, the vast majority of Americans made sure they had plenty of toilet paper but didn’t really stockpile anything else.
Things have changed. There’s a growing anxiety in this presidential election year that has prompted more Americans to get prepared for crazy events in the future. Some of it is being driven by fearmongers, but there are valid concerns with the economy, food supply, pharmaceuticals, the energy grid, and mass rioting that have pushed average Americans into “prepper” mode.
There are degrees of preparedness. One does not have to be a full-blown “doomsday prepper” living off-grid in a secure Montana bunker in order to be ahead of the curve. In many ways, preparedness isn’t about being able to perfectly handle every conceivable situation. It’s about being less dependent on government for as long as possible. Those who have proper “preps” will not be waiting for FEMA to distribute emergency supplies to the desperate masses.
Below are five things people new to preparedness (and sometimes even those with experience) often forget as they get ready. All five are common sense notions that do not rely on doomsday in order to be useful. It may be nice to own a tank during the apocalypse but there’s not much you can do with it until things get really crazy. The recommendations below can have places in the lives of average Americans whether doomsday comes or not.
Note: The information provided by this publication or any related communications is for informational purposes only and should not be considered as financial advice. We do not provide personalized investment, financial, or legal advice.
Secured Wealth
Whether in the bank or held in a retirement account, most Americans feel that their life’s savings is relatively secure. At least they did until the last couple of years when de-banking, geopolitical turmoil, and the threat of Central Bank Digital Currencies reared their ugly heads.
It behooves Americans to diversify their holdings. If there’s a triggering event or series of events that cripple the financial systems or devalue the U.S. Dollar, wealth can evaporate quickly. To hedge against potential turmoil, many Americans are looking in two directions: Crypto and physical precious metals.
There are huge advantages to cryptocurrencies, but there are also inherent risks because “virtual” money can become challenging to spend. Add in the push by central banks and governments to regulate or even replace cryptocurrencies with their own versions they control and the risks amplify. There’s nothing wrong with cryptocurrencies today but things can change rapidly.
As for physical precious metals, many Americans pay cash to keep plenty on hand in their safe. Rolling over or transferring retirement accounts into self-directed IRAs is also a popular option, but there are caveats. It can often take weeks or even months to get the gold and silver shipped if the owner chooses to close their account. This is why Genesis Gold Group stands out. Their relationship with the depositories allows for rapid closure and shipping, often in less than 10 days from the time the account holder makes their move. This can come in handy if things appear to be heading south.
Lots of Potable Water
One of the biggest shocks that hit new preppers is understanding how much potable water they need in order to survive. Experts claim one gallon of water per person per day is necessary. Even the most conservative estimates put it at over half-a-gallon. That means that for a family of four, they’ll need around 120 gallons of water to survive for a month if the taps turn off and the stores empty out.
Being near a fresh water source, whether it’s a river, lake, or well, is a best practice among experienced preppers. It’s necessary to have a water filter as well, even if the taps are still working. Many refuse to drink tap water even when there is no emergency. Berkey was our previous favorite but they’re under attack from regulators so the Alexapure systems are solid replacements.
For those in the city or away from fresh water sources, storage is the best option. This can be challenging because proper water storage containers take up a lot of room and are difficult to move if the need arises. For “bug in” situations, having a larger container that stores hundreds or even thousands of gallons is better than stacking 1-5 gallon containers. Unfortunately, they won’t be easily transportable and they can cost a lot to install.
Water is critical. If chaos erupts and water infrastructure is compromised, having a large backup supply can be lifesaving.
Pharmaceuticals and Medical Supplies
There are multiple threats specific to the medical supply chain. With Chinese and Indian imports accounting for over 90% of pharmaceutical ingredients in the United States, deteriorating relations could make it impossible to get the medicines and antibiotics many of us need.
Stocking up many prescription medications can be hard. Doctors generally do not like to prescribe large batches of drugs even if they are shelf-stable for extended periods of time. It is a best practice to ask your doctor if they can prescribe a larger amount. Today, some are sympathetic to concerns about pharmacies running out or becoming inaccessible. Tell them your concerns. It’s worth a shot. The worst they can do is say no.
If your doctor is unwilling to help you stock up on medicines, then Jase Medical is a good alternative. Through telehealth, they can prescribe daily meds or antibiotics that are shipped to your door. As proponents of medical freedom, they empathize with those who want to have enough medical supplies on hand in case things go wrong.
Energy Sources
The vast majority of Americans are locked into the grid. This has proven to be a massive liability when the grid goes down. Unfortunately, there are no inexpensive remedies.
Those living off-grid had to either spend a lot of money or effort (or both) to get their alternative energy sources like solar set up. For those who do not want to go so far, it’s still a best practice to have backup power sources. Diesel generators and portable solar panels are the two most popular, and while they’re not inexpensive they are not out of reach of most Americans who are concerned about being without power for extended periods of time.
Natural gas is another necessity for many, but that’s far more challenging to replace. Having alternatives for heating and cooking that can be powered if gas and electric grids go down is important. Have a backup for items that require power such as manual can openers. If you’re stuck eating canned foods for a while and all you have is an electric opener, you’ll have problems.
Don’t Forget the Protein
When most think about “prepping,” they think about their food supply. More Americans are turning to gardening and homesteading as ways to produce their own food. Others are working with local farmers and ranchers to purchase directly from the sources. This is a good idea whether doomsday comes or not, but it’s particularly important if the food supply chain is broken.
Most grocery stores have about one to two weeks worth of food, as do most American households. Grocers rely heavily on truckers to receive their ongoing shipments. In a crisis, the current process can fail. It behooves Americans for multiple reasons to localize their food purchases as much as possible.
Long-term storage is another popular option. Canned foods, MREs, and freeze dried meals are selling out quickly even as prices rise. But one component that is conspicuously absent in shelf-stable food is high-quality protein. Most survival food companies offer low quality “protein buckets” or cans of meat, but they are often barely edible.
Prepper All-Naturals offers premium cuts of steak that have been cooked sous vide and freeze dried to give them a 25-year shelf life. They offer Ribeye, NY Strip, and Tenderloin among others.
Having buckets of beans and rice is a good start, but keeping a solid supply of high-quality protein isn’t just healthier. It can help a family maintain normalcy through crises.
Prepare Without Fear
With all the challenges we face as Americans today, it can be emotionally draining. Citizens are scared and there’s nothing irrational about their concerns. Being prepared and making lifestyle changes to secure necessities can go a long way toward overcoming the fears that plague us. We should hope and pray for the best but prepare for the worst. And if the worst does come, then knowing we did what we could to be ready for it will help us face those challenges with confidence.
