Considering Vaccine Injuries Through the Years

(This is the beginning of a much larger article — worth a read if you have any questions or concerns at all about vaccine safety and efficacy.)

How Much Damage Has Mass Vaccination Done to Society?

The data that shows the less appreciated and forgotten consequences of vaccination.

Story at a Glance:

•A long history exists of a wave of severe injuries following new vaccinations being introduced to the market. In most cases, those injuries were swept under the rug to protect the business.

•In many cases, the severe “mysterious” injuries we see now are remarkably similar to those that were observed over a century ago. Unfortunately, a widespread embargo exists on ever allowing this data to come to light (as that would instantly destroy the vaccine program).

•A variety of independent studies (summarized below) have shown that vaccines cause a wide range of chronic illnesses.

•A 1990 book made a strong case that widespread vaccination was also causing an epidemic of widespread brain damage which was both lowering America’s IQ and causing a massive rise in violent crime.

•In this article, we will also review exactly what in that 1990 book and the classic signs that can be used to determine if someone has a vaccine injury (along with the subtle more spiritual ones).

Note: due to the recent ACIP changes (the committee which decides which vaccines you take) and past interest in this article, I revised and updated it.

My mind often overlaps the past present and future onto themselves. Because of this, I will frequently recall events that happened in the past which perfectly mirror what is unfolding before us, and in turn, I’ve lost count of how many times I’ve witnessed humanity repeat its same mistakes or can see a slow motion train-wreck ahead on the horizon. During COVID, I realized we were again reenacting the same tragedy humanity had ever experienced since the smallpox vaccine was brought to the market and I had a thought. If people became aware of what had happened before and ended our collective amnesia, perhaps this could at last stop.

As fate would have it, my wish came true, and without knowing me, Steve Kirsch gave me the opportunity to begin introducing that forgotten history to the world. This happened after he chose to publish an article I wrote illustrating how the trucker protests were identical to smallpox protests that had happened more than a century before and then for reasons I still do not understand, encouraged his readers to subscribe to me so I would start writing here.
Note: At the time I chose the username “A Midwestern Doctor” (for the smallpox article), I did not put much thought into it as I was never expecting to use it again.

Over the years, I’ve noticed again and again that a vaccine disaster happens which injuries many in a very similar way, it gets swept under the rug (often by officials who are quite conflicted in their decision to do so), and then the same thing happens again a few decades later.

Given that we give dozens of vaccines to each member of society, this raises an obvious question—what is that doing to society?

A Brief History of Vaccine Disasters

In 1798, the smallpox vaccine hit the market. Once it hit the market, it was observed to frequently cause smallpox outbreaks (rather than prevent them) and to cause a wide range of debilitating and complex injuries that many of the doctors had never seen before (and many of which I believe were examples of “blood stasis”). Curiously, rather than recognizing this was a mistake, most of the medical profession endorsed the smallpox vaccine, and governments around the world mandated it as cases kept on increasing, leading to a downward spiral that was eventually broken by mass public protest against those mandates. Having looked at it extensively, I am of the opinion the smallpox vaccine reshaped the trajectory of humanity’s health and was an inflection point in the era of chronic illness.

In the 1800s and early 1900s, a variety of early vaccines (e.g., rabies, typhoid, diphtheria, tuberculosis) and horse-generated antiserums (for most of the common infections at the time) entered the market. Since many of these vaccines were produced in small independent labs, there were a variety of quality control issues with these products, which frequently led to hot lots being released that severely injured or killing a group of people. Additionally, many of those vaccines had a high degree of toxicity. Because of this, a variety of new and severe medical conditions emerged, many of which were deemed to be due to brain inflammation (encephalitis) or brain damage (encephalopathy) and observed to occur in conjunction with cranial nerve damage. Most of these conditions (which I discussed in detail here) in turn mirrored the myriad of injuries we now too see from modern vaccinations. In addition to the injuries, two major issues stood out during this period:

•First, in addition to sometimes being directly contaminated with the disease causing organism (e.g., yellow fever or tuberculosis) and causing the illness, vaccines would often cause a temporary immune suppression which lead to disease outbreaks in those vaccinated (discussed here). However, each time this happened, rather than it being seen as a sign we needed to dial back vaccination, it was interpreted as not enough people being vaccinated and harsher and harsher vaccine mandates being instituted to enact that policy or new vaccines being created to address the existing damage of vaccination (e.g., the DPT vaccine frequently caused polio outbreaks).

•Second, public health officials and vaccine designers were well aware of the injuries vaccines were causing, but since no other treatments existed for the disease, regrettably deemed this to be a necessary sacrifice for the greater good and hence covered the injuries up so the public would continue to vaccinate. However, while I understand their perspective, it rested on a faulty premise—effective treatments did exist for the illnesses (e.g., in 1920 it was known IV hydrogen peroxide could treat severe infections and in 1928 it was known that ultraviolet blood irradiation could treat many otherwise incurable infections).
Note: as you might have noticed, everything I just described also applies to the COVID-19 vaccines, hence illustrating how these dysfunctional cycles frequently perpetuate indefinitely.

In the 1940s-1950s, the original pertussis vaccine (DPT) entered the market. This vaccine excelled at causing brain inflammation and a variety of concerning differences were seen in the generations born after its mass adoption in America.
Note: The rabies vaccine also excelled at causing encephalitis (around 1 in 750 injections, of which 20% were fatal), but it did not have as large an impact on society because far fewer people received it.

Between the 1950s to 1970s, numerous instances happened where a rushed and poorly produced experimental vaccine (e.g., polio or the swine flu) was brought to market to address a non-existent “emergency,” and the government chose to ignore warnings from its scientists that it was not safe to give to America. Since the press was honest at this time, they reported the disaster, it became a national scandal and the government provided compensation to the victims.
Note: I compiled those media reports here, the last of which happened in 2002 with Bush’s smallpox vaccine.

In 1986, enough public awareness existed of the dangers of the DPT vaccine that lawsuits were regularly being filed for the brain damage and sudden infant deaths it caused (discussed here). This in turn led to the 1986 vaccine injury act being passed (discussed further here), an act that both shielded vaccine manufacturers from product liability and was intended to help parents of vaccine injured children (even though it didn’t due to selective enforcement of its provisions and the Supreme Court exempting manufacturers from injuries caused by defective vaccines). This act being passed led to an industry gold rush to bring experimental and liability free vaccines to the market, and before long the childhood vaccination schedule ballooned in parallel to chronic illnesses increasing as well.

Note: since this time other vaccines (e.g., RSV and annual COVID vaccinations) were also added to the childhood schedule (but fortunately MAHA managed to recently do the impossible and remove COVID from it).

In 1990, an experimental anthrax vaccine was deployed upon the military to prepare them for invading Iraq. While the war was non-eventful (Saddam did not use anthrax and it was likely the most one-sided conflict in history), the anthrax vaccine severely injured over 100,000 servicemen (leading to what was known as Gulf War Syndrome). Despite these issues, individuals within the Department of Defense who were committed to funding their bioweapons defense program mandated it—leading to severe injuries throughout the military and widespread rebellion against this edict.

After this, new biotechnologies began emerging which made it possible to genetically engineer a plethora of new vaccines that then began to flood the market as ACIP endorses virtually every vaccine given to them regardless of its merits (in fact, throughout their dozens of endorsements I could only identify one case where ACIP did not [boosters for teachers and healthcare workers], and in that instance the CDC simply overrode ACIP). In tandem, direct to consumer pharmaceutical advertising was legalized by a 1997 FDA decision, making it possible for the pharmaceutical industry to buy the mass media’s silence, and hence end all future coverage of vaccine injury.

In 2010, Merck convinced America’s women they were at a high risk of dying from cervical cancer (which in reality only kills about 1/38,000 American women each year) so that everyone would buy their highly lucrative vaccine (which was never proven to reduce cervical cancer deaths). This vaccine had an extraordinarily high rate of injuries (e.g., severe autoimmune disorders), but nonetheless, despite a deluge of complaints, the CDC and FDA did everything they could to protect it, and to this day it is still mandated for children.

In 2021, the COVID vaccine hit the market and caused an unprecedented amount of injury (e.g., many noticed healthy adults dying “suddenly” and large polls showed 34% of vaccine recipients reported minor side effects while 7% reported major ones severely impacting their quality of life). Fortunately or unfortunately, the rate of injuries from it was so high that unlike the past disasters, the mass media could no longer sweep it under the rug, which eventually culminated in MAHA ascending as a political force and RFK Jr. being put in charge of the agency which has orchestrated the vaccine disaster for decades.

In my eyes, one of the most important points to take from this history is that at the time each of these happened, the medical profession and public were struck by the explosion of these new diseases (and their immense social cost) but before long, became acclimated to them and forgot they had ever emerged in the first place.

The Harms of Vaccination

There is a large body of evidence suggesting vaccines are either solely responsible for, or one of the primary things responsible for the tsunami of chronic illness which has followed their ever-increasing adoption.  …

to read the rest go to:    https://www.midwesterndoctor.com/p/how-much-damage-has-mass-vaccination?publication_id=748806&post_id=166011036&isFreemail=true&r=19iztd&triedRedirect=true&utm_source=substack&utm_medium=email

Spiritual? Religious? Not Any More!!!

Destroying Our Connection to God with Gene Editing Injections

The VMAT2 gene is a protein that carries several vital neurotransmitters to synapses in the brain. It basically controls the central nervous system. Deleting it, known as a knockout, would greatly reduce these neurotransmitters creating an endless list of chronic health issues. CRISPR technology, which is sold online, can edit and delete VMAT2. Dr. Ariyana Love asks, “How long have pharma and the government been reducing our humanity through VMAT2 knockouts?”

Link for video:      https://www.bitchute.com/video/z9gX2kvxFB6U/

More than a hundred years ago, Rudolf Steiner wrote that. “In the future, we will eliminate the soul with medicine. Under the pretext of a ‘healthy point of view’, there will be a vaccine by which the human body will be treated… so that the human being cannot develop the thought of the existence of soul and Spirit… He would be extremely smart, but he would not develop a conscience, and that is the true goal of some materialistic circles.”

A viral video which claims to be a leaked 2005 presentation to the DOD by American geneticist, Dean Hamer, shows a man briefing a room of men about the VMAT2 gene, the God gene, and how it can be suppressed with the use of vaccines.

“Excuse me, on the left over here, we have individuals who are religious fundamentalists, religious fanatics. And this is the expression, RTPCR, real time PCR, expression of the VMAT2 gene. Our hypothesis is that these are fanatical people, that they have overexpression of the VMAT2 gene and that by vaccinating them against this, we’ll eliminate this behavior.”
~ Dean Hamer (Fake)

In 2021, former NEWS anchor, Ryan Harper, claimed in the San Francisco Chronicle that he created this video as a short film. But has provided no clear evidence to substantiate this claim. And if it is a hoax, then it appears to be disinformation, False information deliberately spread to employ strategic deceptions to advance political, military, or commercial goals. Because in 2009, Dean Hamer lectured at Marlboro College about this same subject.

“Well, it turns out at least one gene that’s involved in spirituality has now been identified. It's one of many different players. The next slide shows it. It's something called The Vesicular Monoamine Transporter number 2.”
~ Dean Hamer (Real)

And in 2004, Hamer published the book, “The God Gene: How Faith Is Hardwired into our Genes,” where in he argues that a variation in the VMAT2 gene dictates one’s openness to spiritual experiences, and without it, we can not feel God.

Not only is this information accurate, but it appears to have been deployed. In a recent article by Dr Ariyana Love, it is shown that this technology has existed for years.

The VMAT2 gene is a protein that carries several vital neurotransmitters to synapses in the brain. It basically controls the central nervous system. Deleting it, known as a knockout, would greatly reduce these neurotransmitters creating an endless list of chronic health issues.

VMAT2 deletion is accomplished using the “SLC18A2 cDNA ORF clone” where “cDNA” is “Complimentary DNA.” Which is used in human cloning and genetically modifying an organism. In 2013, Supreme Court judges ruled that cDNA added to target cells in the human genome, makes a person patent eligible. And there are patents for using this to genetically edit the human VMAT2 gene and delete it. This can easily be done using simple CRISPR technology and is even sold online.

In a 2020 study on mice, VMAT2 gene deletion caused schizophrenia. In a 2022 study it caused Parkinson’s disease. In the American Journal of Human Genetics, a study on deleting the VMAT2 induces an “Intellectual Disability Syndrome” in humans. It causes autoimmune disorders, cerebral palsy, type 1 diabetes, and several other illnesses. Begging the question, as Dr. Love asks, “How long have pharma and the government been reducing our humanity through VMAT2 knockouts?”

VMAT2 deletion also causes fearfulness, psychiatric disorders, cardiac arrhythmia, cancer, and accelerated aging. While it’s unlikely that these sadistic mad scientists can cut us off from God, they are definitely doing their best to murder us.

Read full article here…

from:    https://needtoknow.news/2024/05/destroying-our-connection-to-god-with-gene-editing-injections/

What Cost – Clean Blood?

Researchers Call for Urgent Action to Address Mass Contamination of Blood Supply

May 27, 2024
blood supply contamination

STORY AT-A-GLANCE

  • Japanese researchers warn of the risks of using blood from mRNA COVID vaccine recipients, highlighting potential deadly effects and the need for urgent action to secure the global blood supply
  • Blood contaminated with prion-like structures from the spike protein raises the risk of inducing fatal neurodegenerative diseases in recipients. The potential transmission of harmful proteins through exosomes (“shedding”) and the risk of autoimmune diseases due to the vaccines’ mechanism and components like lipid nanoparticles (LNPs) are other major concerns
  • Proposals for managing blood collection include rigorous donor interviews, deferral periods, and a suite of tests to ensure the safety of blood products
  • The researchers advocate for comprehensive testing of both jabbed and unjabbed individuals to assess the safety of blood products and suggest discarding blood products contaminated with spike proteins or modified mRNA until effective removal methods have been developed
  • They call for suspending all gene-based “vaccines” and conducting a rigorous harm-benefit assessment in light of the serious health injuries reported. They also urge countries and organizations to take concrete steps to address and mitigate the already identified risks

In a recent meta-analysis1,2 posted on preprints.org, Japanese researchers warn of potentially deadly risks to patients who receive blood from people who have taken mRNA COVID jabs and call for urgent action to ensure the safety of the global blood supply. According to the authors:3

“… many countries around the world have reported that so-called genetic vaccines, such as those using modified mRNA encoding the spike protein and lipid nanoparticles as the drug delivery system, have resulted in post-vaccination thrombosis and subsequent cardiovascular damage, as well as a wide variety of diseases involving all organs and systems, including the nervous system …

[B]ased on these circumstances and the volume of evidence that has recently come to light, we call the attention of medical professionals to the various risks associated with blood transfusions using blood products derived from people who have suffered from long COVID and from genetic vaccine recipients, including those who have received mRNA vaccines, and we make proposals regarding specific tests, testing methods, and regulations to deal with these risks.”

Blood From Jabbed Donors May Pose Risk to Neurological Health

One particular risk addressed in this paper is the implications of blood tainted with prion-like structures found within the spike protein. Prions are misfolded proteins that can cause neurodegenerative diseases, such as Creutzfeldt-Jakob Disease (CJD) in humans, by inducing the misfolding of normal proteins in the brain.

Prion diseases are characterized by a long incubation period, followed by rapid progression and high mortality. The suggestion that the spike protein of SARS-CoV-2, especially from certain variants, might contain prion-like domains raises concerns for several reasons:

  • Transmission risk — If spike proteins with prion-like structures can be transmitted through blood transfusions, there might be a risk of inducing prion diseases in recipients. Prion diseases are notoriously difficult to diagnose early, have no cure, and are fatal, making any potential transmission through blood products a significant safety concern.
  • Detection and removal challenges — Current blood screening processes do not specifically test for prions, partly because prion diseases are rare and partly due to the technical challenges in detecting prions at low concentrations. If spike proteins with prion-like properties are present in the blood of COVID jabbed individuals, existing blood safety protocols may not be adequate to prevent transmission.
  • Long-term safety concerns — Prion diseases have long latency periods, meaning that symptoms can appear years or even decades after exposure. This delay complicates efforts to trace the source of an infection back to a blood transfusion and assess the safety of blood supplies over time.
  • Impacts on blood supply management — Concerns about the potential risks associated with prion-like structures in spike proteins might lead to changes in donor eligibility criteria or the implementation of additional screening measures. These changes could impact the availability of blood products, which are critical for routine medical procedures.
  • Public confidence — Public awareness of these potential risks, even if they are theoretical or have a very low likelihood of occurring, could affect individuals’ willingness to donate or receive blood transfusions, thereby lowering blood donation rates and the overall trust in the safety of blood transfusions.

The authors stress the need for comprehensive studies to better understand the implications of these prion-like structures in the spike protein, not only for mRNA jab safety but also for the broader implications for public health measures like blood transfusion practices.

Other Potential Health Hazards of Contaminated Blood

Contaminated blood may also pose other serious health risks, including:

Reduced immune function among blood recipients — It’s been shown that the more doses of the COVID shot you’ve received, the more likely you are to suffer future infections, either by SARS-CoV-2 or other viruses, due antibody-dependent enhancement.

Blood donations from people who have received several doses of mRNA injections may not provide adequate immunity against common infections, resulting in subclinical infections and diseases in recipients.

Formation of blood clots and amyloid aggregates — If the immune system of a blood recipient isn’t strong enough to neutralize spike protein, blood clots and amyloid aggregates may also form.

Chronic inflammation — Prolonged exposure to the antigens from the COVID-19 shots can trigger the generation of IgG4 antibodies, resulting in chronic inflammation and immune dysfunction.

IgG4 antibodies are often associated with chronic exposure to antigens, such as those seen in persistent infections, certain cancers, and prolonged exposure to allergens. IgG4 antibodies are also associated with a unique condition known as IgG4-Related Disease (IgG4-RD), a fibro-inflammatory condition characterized by swellings or masses in affected organs.4

Blood Transfusions and the Risk of Autoimmune Diseases

The authors also raise concerns about the potential of contaminated blood to cause autoimmune diseases in recipients. Recent research found that the RNA pseudouridylation, a process in which uracil is swapped out for synthetic methylpseudouridine, can cause frameshifting, basically a glitch in the decoding, which can trigger the production of off-target aberrant proteins.

The antibodies that develop as a result may, in turn, trigger off-target immune reactions. In addition to that, lipid nanoparticles (LNPs), a key component of the COVID shots, have been identified as highly inflammatory and possessing more potent adjuvant activity compared to traditional vaccine adjuvants, which further increases the risk of an autoimmune response. As reported in the featured paper:5

“Recent studies have shown that RNA pseudouridylation can result in frameshifting. It is not yet clear whether a portion of the pseudouridinated mRNA for the spike protein is translated into another protein of unknown function in vaccine recipients. If these proteins are also pathogenic, additional testing for such frameshift proteins may be needed in the future.

Even if a frameshift protein is not toxic, it must be foreign to the body and could cause autoimmune disease. In addition, LNPs themselves are highly inflammatory substances … LNPs have been found to have stronger adjuvant activity than the adjuvants used in conventional vaccines, and there is also concern about autoimmune diseases resulting from this aspect.

Thus, although it is not clear what the causative agent of autoimmune disease is, the large number of reported cases of autoimmune disease following genetic vaccination is extremely concerning.

The very mechanism of gene vaccines that causes one’s own cells to produce the antigens of pathogens carries the risk of inducing autoimmune diseases, which cannot be completely avoided even if mRNA pseudouridylation technology is used.

In this context, individuals with a positive blood test for spike protein may need to have interviews and additional tests for autoimmune disease indicators, such as antinuclear antibodies.

Alternatively, if the amino acid sequence of the protein resulting from the frameshift is predictable, these candidate proteins could be included in the initial mass spectrometry assay. In any case, it is particularly important to develop tests and establish medical care settings in anticipation of these situations.”

Proposals for Managing Blood Collection

The authors outline several specific proposals for managing blood collection and blood products from individuals who have received genetic “vaccines.” Given the variety of blood-related abnormalities observed post-jab, the researchers argue that rigorous and precautionary measures in blood handling and transfusion practices have now become a necessity.

A key part of the proposal involves conducting thorough interviews with potential blood donors. These interviews should cover their vaccination status, number of doses received, their COVID-19 infection history, and any symptoms they might be experiencing that could indicate conditions like post-vaccination syndrome (PVS), long-COVID or other complications.

The researchers also recommend deferral periods for blood collected from COVID jab recipients — 48 hours for mRNA shots and six weeks for AstraZeneca DNA jab recipients. A series of tests are also proposed to ensure the safety of collected blood, including:

Mass spectrometry to measure spike protein content PCR for detecting the presence of spike protein mRNA and DNA
Testing for markers associated with autoimmune disorders Enzyme-linked immunosorbent assay (ELISA)
Immunophenotyping Liquid biopsies combined with proteomics to detect and quantify spike protein and its mRNA

The authors also note that policies and procedures must be constantly revised as new risks and problems with blood products derived from mRNA and DNA jab recipients are identified.

Ensuring Safety of Current Blood Products

The paper also reviews strategies to ensure the safety of blood products already collected, highlighting the complex challenges that medical institutions, regulatory bodies, and the broader healthcare ecosystem must navigate in the wake of widespread use of mRNA injections.

The primary concern is the risk posed to patients by the use of blood products from donors who have received gene-based injections without confirming the presence or absence of spike proteins or modified mRNA. To ensure their safety, methods to quantify potential contaminants must be developed and implemented as soon as possible.

Another critical issue that must be addressed is the current lack of reliable methods to remove spike proteins or modified mRNA from blood products. The authors warn that, given the potential persistence, low solubility, heat resistance, and radiation resistance of these components, current methodologies are inadequate for the job. The only solution, they say, is to discard all blood products found to contain these contaminants until effective removal techniques are established.

Researchers Call for Widespread Blood Testing

Additionally, the researchers call for widespread testing of both jabbed and unjabbed to assess the potential transmission of spike proteins through exosomes (so-called shedding).

As noted by the authors:

“… when exosomes collected from vaccine recipients were administered to mice that had not been vaccinated with the genetic vaccine, the spike protein was transmitted.

Therefore, it cannot be denied that the spike protein and its modified genes can be transmitted through exosomes. For this reason, we suggest that full testing be done initially, regardless of genetic vaccination status, and that a cohort study be conducted to quickly capture the full picture …

In addition … it cannot be ruled out that even those who have not been vaccinated with the genetic vaccine, but have had long COVID, may have residual spike proteins or fibrin- derived microthrombi in their bodies, so it would be advisable to conduct the same testing and follow-up as for genetic vaccine recipients.

The presence or absence and amount of anti-nucleocapsid antibodies as well as antibody isotypes may be an indicator(s) in distinguishing whether genetic vaccination or long COVID is the cause. In any case, these cohort studies are expected to help establish cutoff values for blood levels of spike protein and other substances to determine the safety of blood products.

Faksova et al. conducted a large cohort study of 99 million people using a multinational Global Vaccine Data NetworkTM (GVDN®) and found a significantly increased risk of myocarditis, pericarditis, Guillain-Barre syndrome, and cerebral venous sinus thrombosis in genetic vaccine recipients.”

Ensuring the traceability of blood products and establishing a rigorous legal and regulatory framework to manage the myriad issues arising from the use of blood products derived from COVID jabbed individuals are also paramount. This includes creating systems for the registration of all potential donors, ensuring the traceability of blood products, and conducting recipient outcome studies.

Call to Pause: Evaluating the Risks and Benefits of Genetic Vaccines for a Safer Future

In conclusion, the authors point out that if we continue using mRNA-LPN-based platforms to replace conventional vaccines or create new ones, then the risks to our blood and bone marrow supply will be augmented further.

“The impact of these genetic vaccines on blood products and the actual damage caused by them are unknown at present,” they write.6

“Therefore, in order to avoid these risks and prevent further expansion of blood contamination and complication of the situation, we strongly request that the vaccination campaign using genetic vaccines be suspended and that a harm-benefit assessment be carried out as early as possible, as called for by Fraiman et al.7 and Polykretis et al.8

[T]he health injuries caused by genetic vaccination are already extremely serious, and it is high time that countries and relevant organizations take concrete steps together to identify the risks and to control and resolve them.”

from:    https://articles.mercola.com/sites/articles/archive/2024/05/27/blood-supply-contamination.aspx?ui=f460707c057231d228aac22d51b97f2a8dcffa7b857ec065e5a5bfbcfab498ac&sd=20211017&cid_source=dnl&cid_medium=email&cid_content=art1HL&cid=20240527&foDate=true&mid=DM1578458&rid=32119642