Category: Vaccines

• Environmental allergies affect 20% of Americans, causing a total of 4 million lost workdays and $8 billion in annual economic losses. Kaempferol, found in leafy greens, shows promise in natural allergy relief
• The intestinal enzyme RALDH2, boosted by kaempferol, converts vitamin A-derived retinal to retinoic acid, which helps suppress allergic immune responses through regulatory T-cell development
• Following an elimination diet will help identify food allergies, but complete avoidance isn’t recommended as it leads to malnutrition
• Vitamin C (300 to 500 milligrams daily) demonstrates antihistamine properties, reducing plasma histamine levels by 40% over two weeks, with red peppers, citrus fruits and parsley being excellent natural sources
• Quercetin, particularly abundant in onion skins, apples and berries, shows significant antiallergy activity by modulating histamine release, with recommended doses of 500 to 1,000 milligrams taken twice to four times daily

…”The rapid decrease in body temperature and allergic diarrhea observed after… …administration were significantly suppressed in mice that were administered kaempferol.”

Kaempferol is abundant in leafy green veggies, such as broccoli, spinach and cabbage. According to a study published in Molecules, broccoli happens to have the highest concentration, while blueberries and onions are also good choices…

…

In the video above,19 Dr. Jin Sung explains the role of quercetin in helping relieve seasonal allergies. According to his findings, he believes that quercetin possesses the greatest antiallergy activity compared to other flavonoids. Specifically, it works by modulating the release of histamine from basophils and mast cells. This process was also documented in a study published in Biomedicine & Pharmacotherapy.

When it comes to dosing, Sung recommends taking 500 to 1,000 mg of quercetin, two to four times a day during allergy season to help manage the symptoms. Begin with the lowest dose first — 500 mg, twice a day — and gradually increase if necessary. The reason for this is because the half-life of quercetin is 3.5 to 7.5 hours, so it’s best taken in divided doses.

To help improve the results, I recommend taking other supplements to create synergistic effects. These include stinging nettle, butterbur extract, mangosteen extract, ginger, vitamin C and vitamin D.

Like vitamin C and kaempferol, quercetin is also found in many whole foods. These include citrus fruits, green leafy vegetables, broccoli, apples, onions, green tea, red grapes, dark cherries and berries, such as blueberries and cranberries. From these examples, the highest amounts are found in apples — especially the skins — as well as onions, broccoli, cherries, berries and green tea.

https://nexusnewsfeed.com/article/health-healing/kaempferol-a-potent-antiallergic-flavonoid/

This confirms what was observed about LNPs (Lipid Nano-Particles) in Pfizer’s biodistribution study done during its mRNA COVID “vaccine” clinical trial. “These data demonstrate that COVID-19 mRNA injection LNPs systemically circulate and are taken up into vital organ systems resulting in body-wide toxic Spike protein production. This helps to explain why autopsies find widespread dissemination of ‘vaccine’ spike protein in various tissues and organs.”

https://petermcculloughmd.substack.com/p/breaking-study-intramuscular-mrna

In the post-pandemic period, there were two particularly appalling and incontrovertible studies about the mRNA jabs that more than anything else started the slow reversal of science’s great stampede toward genetic therapies. The first was actually a group of studies, led by Kevin McKernan, confirming the shots were contaminated with DNA fragments of bacteria normally found in human waste. (Literally, “s— shots.”) The second was a gold-standard study finding “frame-shifting” (mutational drifts) in the induced spike proteins. Yesterday we received a third seminal study to help sink the shots and the Frankenstein’s nightmare called mRNA technology.

The peer-reviewed study published yesterday in the prestigious Nature Biotechology, titled “Nanocarrier imaging at single-cell resolution across entire mouse bodies with deep learning.” It had forty authors. There’s safety in numbers. They cautiously avoided criticizing the covid shots directly, but the implications were unavoidable.

This study investigated lipid nanoparticles (LNPs), which are the tiny globs of fake fat that deliver mRNA into cells. They tracked the LNPs’ distribution and effects throughout the body—which they found far beyond the injection site. The researchers found that even at very low doses, LNPs wander far afield and worse, they accumulate in unintended organs, triggering immune disregulation and metabolic disturbances.

The study’s carefully documented conclusion upended the government’s original claims the mRNA vaccines would remain “localized at the injection site” (i.e. that they’d quickly and harmlessly dissolve in your shoulder). The findings also provided a plausible explanation for what causes serious known side effects like myocarditis.

These findings aren’t altogether new. They align with earlier findings from a widely ignored 2022 Japanese biodistribution study. The difference now, though, is these scientists used cutting-edge imaging technology to track LNPs in mice, and they used A.I. to analyze very complex data sets (such as systemic effects with multiple variables) and for modeling simulations at various LNP dosages.

There are several levels here. Superficially, the FDA should urgently re-examine the biodistribution issue and immediately require the shotmakers to confirm these findings and study the long-term effects and implications. Of course, we all know the benighted FDA will do nothing of the kind, at least not for five more days.

Next, and more significantly, the study further undermined the foundations not just of the covid shots, but of mRNA technology writ large. This week, Moderna —a pharma firm that only develops mRNA drugs— lost a fifth of its stock value on news of actual sales far below original, conservative projections.

But now we also know that Moderna’s stock plunge preceded the publication of this new biodistribution study by a single day. That timing was probably not coincidental.

The study’s findings reveal the third structural problem with mRNA. Until those structural problems are solved, or even addressed, mRNA risks becoming nothing more than a forgettable footnote in the sordid history of scientific failure: a tragic tale of overpromised innovation and blind faith in cutting-edge technology, calamitously unraveled by unmet safety and efficacy standards.

And that is assuming things don’t get any worse. Which is the point—we don’t know. This study provided no reassurances. And it probably poisons all mRNA projects.

Take, for instance, the long-promised vision of using mRNA to deliver customized cancer cures. The concept involves encoding the mRNA with some protein from your specific cancer, in theory prompting the body to mount a targeted immune response. But so long as the treatment relies on lipid nanoparticles (LNPs) to deliver its mRNA payload, this study suggests a potentially catastrophic risk: the cancer protein could unintentionally transfect major off-target organs like the heart, liver, kidneys, and spleen, potentially spreading cancerous material throughout the body while simultaneously disrupting the immune system.

Needless to say, that would be a bad combination. Unless we are missing something, the future of targeted mRNA cancer treatments does not look bright. As for respiratory viruses, that ship has already sailed.

The truth continues to dribble out. This study presented an unavoidable obstacle to all future mRNA development, a new reveal that joins and combines with the first two major revelations. This most terrible idea of mRNA is not yet dead, not quite, but all of mRNA’s major organ systems have been infected, and it’s been moved to hospice, leaving its loudest proponents languishing in the denial stage of grief.

This study is extraordinary progress. It really does seem like everything sad is coming untrue, slowly perhaps, maybe bit by bit, but it is happening.

http://publication_id=463409&post_id=154888913&triggerShare=true&isFreemail=true&r=yh8aw&triedRedirect=true

The U.S. Food and Drug Administration (FDA) on Tuesday flagged at least five cases of “severe/very severe” RSV lower respiratory tract infections in infants who received Moderna Inc.’s mRNA RSV injections mRNA-1345 and mRNA-1365.

This means that those injected with Moderna’s mRNA RSV shot are becoming severely infected with RSV.

In other words, the shot is not only not working, but the vaccinated are getting the very disease the vaccine is supposed to protect from.

Alarmingly, the FDA confirmed that 26.3% of infants who received Moderna’s mRNA RSV shot came down with symptomatic RSV that “progressed to severe illness,” compared to only 8.3% in the non-vaccinated group.

This means individuals vaccinated with Moderna’s RSV vaccine were 3.17 times (or 18 percentage points) more likely to become severely infected with RSV than the unvaccinated.

https://jonfleetwood.substack.com/p/infants-vaccinated-with-moderna-rsv

In a Dec. 8 interview with Meet The Press, Trump remarked that autism cases have increased in recent decades. When asked if Kennedy would explore the issue, Trump said he is “open to anything.”

“When you look at some of the problems, when you look at what’s going on with disease and sickness in our country, something’s wrong,” Trump said. “I think somebody has to find out. If you go back 25 years ago, you had very little autism. Now you have it.”

As readers of this Substack are aware, Robert F. Kennedy, Jr. has long been concerned about the possible link between childhood vaccines and autism. He found it especially notable that the incidence of autism began to rise rapidly in the late 1980s, shortly after the passage of the 1986 National Childhood Vaccine Injury Act, which granted vaccine manufacturers immunity from all civil and criminal liability for injuries or deaths caused by their products.

https://petermcculloughmd.substack.com/p/trump-rfk-jr-will-study-possible

Rutin also has strong free radical scavenging properties and protects against DNA damage.

https://wmcresearch.substack.com/p/friday-hope-rutin-inhibits-sars-cov

In 1954, a woman called Bernice Eddy was a lab scientist at NIH performing safety tests for the Polio vaccines. Salk’s inactivated polio vaccine was a killed-virus vaccine to be used in a massive national vaccination program. After testing the vaccines on monkeys, she and her team discovered that the vaccine contained residual LIVE polio virus, resulting in the monkeys showing polio-like symptoms and paralysis. These findings pointed to a flawed vaccine manufacturing process. Eddy reported her findings, and she was immediately dismissed from the polio research and given what we today call “whistleblower treatment.”

The flawed vaccine and associated flawed manufacturing process were licensed for public use. 120,000 polio vaccine doses containing an improperly inactivated version of the live polio virus were manufactured and produced. Of children who received the vaccine, 40,000 developed abortive poliomyelitis, 51 developed paralytic poliomyelitis—and of these, five children died from polio. The exposures led to an epidemic of polio in the families and communities of the affected children, resulting in the death of 5 children and 113 others paralyzed.

https://www.malone.news/p/inconvenient-history-of-salk-inactivated

Walter M Chesnut writes: This article provides additional evidence supporting my hypothesis that demyelination may be a reason behind the staggering increase in Sudden Cardiac Deaths.

https://wmcresearch.substack.com/p/montgomery-et-al-publish-an-article

A new study published this weekend in the peer-reviewed journal International Journal of Vaccine Theory, Practice, and Research has revealed a significant association between indirect exposure to COVID-19 vaccinated individuals and the onset of menstrual irregularities among unvaccinated women.

The study reports that “indirect exposure to COVID-19 vaccinated persons was significantly associated with the likelihood of the onset of menstrual irregularities.”

Among unvaccinated participants who were in close proximity to vaccinated individuals:

• 71.7% reported symptoms within one week.
• 50.1% reported symptoms within three days.

Researchers further identified that “the strongest association lies within the comparison of ‘Daily within 6 feet outside the household’ versus ‘Seldom/Sometimes/Daily outside 6 feet,’” with relative risks of 1.34 for heavier menstrual bleeding, 1.28 for early periods, and 1.26 for extended bleeding.

This means that women who were in daily close proximity to vaccinated individuals were 34% more likely to experience heavier menstrual bleeding, 28% more likely to have an early period, and 26% more likely to have extended bleeding compared to those with less frequent or more distant exposure.

The study raises significant concerns about shedding—the excretion and potential environmental spread of vaccine components, such as lipid nanoparticles (LNPs) and spike proteins.

The authors explain:

“The lipid nanoparticles (LNP), which are the packaging for the mRNA, have also been shown to have wide biodistribution in rodent studies… LNPs are primarily excreted from the experimental animals through feces and urine but also via saliva, sweat, breastmilk, or exhalation.”

The researchers further describe the possible transmission routes for these components, stating:

“The proposed transmission routes to others include inhalation (aerosol), breast milk, transdermal (through keratinocytes), and transplacental.”

Additionally, they note:

“There is accumulating evidence that there can be vaccine component or antibody transmission following COVID-19 vaccination, including via exhaled breath aerosol.”

https://jonfleetwood.substack.com/p/exposure-to-covid-19-jabbed-persons

(Tom: Another example of why detoxing the body of the Spike Protein is so important. https://www.healthelicious.com.au/NutriBlast-Anti-Spike.html