The massive power outage that struck Europe crippling critical infrastructure across much of Spain and Portugal was initially blamed on rare solar flares. However, emerging data now points to vulnerabilities in the power grid tied to the net-zero transition and growing reliance on renewable energy sources.
Red Meat Allergy Surges Across America as WEF’s ‘Human Engineering’ Blueprint Becomes Reality
Fact checked by The People’s Voice Community
May 13, 2025Baxter Dmitry
A dangerous tick-borne illness that leaves victims unable to eat red meat is quietly spreading across the U.S., raising alarms years after the World Economic Forum floated the idea of using the ticks in a “human engineering” scheme to curb global meat consumption.
Known as Alpha-gal Syndrome (AGS), the condition is caused by the bite of the Lone Star tick, which injects a sugar molecule called alpha-gal into the body. This molecule triggers a potentially severe allergic reaction to red meat and other mammal-based products.
According to the Centers for Disease Control and Prevention (CDC), more than 110,000 suspected cases of Alpha-gal Syndrome were reported between 2010 and 2022, however the true number is believed to be much higher due to underdiagnosis and lack of awareness in the medical community.
“Every week, I hear of more cases near me,” said Dr Ben Braddock. “Some farmers and ranchers can’t even go near their livestock. The government needs to treat this with much more urgency.”
In a 2016 panel discussion at the World Science Festival, bioethicist Dr. S. Matthew Liao explored speculative ideas about “human engineering” to address climate change, including reducing meat consumption.
Liao mentioned the Lone Star tick’s possible role in “engineering” humanity by causing red meat allergies, heralding the possibility as an example of how biology can influence dietary habits. (See link for article and video)
‘Fact checkers’ are frantically debunking this, by stating only the lone star tick transmits it, but here’s the deal: AGS is relatively new. Scientists don’t have a clue what and how many ticks can transmit it.
Gates is also behind the manufacture of GM mosquitos that have been released creating hybrid wild mosquitoes.
History has proven that proclaiming a tick only transmits this or that eventually ends up being proven false.
So far the following ticks have been identified as perps for AGS:
Asian longhorned tick has caused AGS in Asia, but the tick has made its way here to the U.S.
Cayenne tick found in South Texas and Florida has also been linked to AGS in Central America.
As recently as April, 2025 a pair of research papers for the FIRST TIME have identified that black-legged ticks and western black-legged ticks can also cause AGS. Please note this evidence has not been obtained by lab experiments, but a case study of a woman who developed the condition after being bitten by a western black-legged tick and a case study of another woman after being bitten by a black-legged tick.
Until ticks, birds, mammals, and reptiles get the memo that they aren’t supposed to cross boundary lines, good luck stopping them from showing up where they shouldn’t be and transmitting stuff they shouldn’t have!
I find it mind boggling that there are NO lab experiments determining what ticks transmit this considering the anaphylactic shock from it can be fatal
Plus, are you sitting down?
You don’t even need a tick bite to get this. To my knowledge, the only reason ticks have been blamed at all is because certain tick’s saliva contains trace quantities of a sugar, alpha-gal, a known human irritant that many researchers and clinicians believeinduces the dangerous allergic responses that are the hallmark of AGS. But, just because you believe something, doesn’t make it true.
Not everyone bitten by a tick containing AGS will develop AGS and not everyone who carries antibodies to AGS will get AGS, and a positive test does not always mean a person has been exposed to alpha-gal. Confused yet?
Some farmers can’t go near their livestock, and for some, it’s not just meat, it’s any product made from mammals like lard, milk, cream, ice cream, cheese, gelatin, lanolin, glycerin, collagen, jello, medications, anti-venom, surgical mesh, carrageenan, ‘natural flavorings’, tallow, and vaccines.
Regarding anaphylaxis: A 2021 study described cases of severe anaphylaxis in individuals receiving vaccines containing gelatin. The authors stated:
“Gelatin-containing vaccines should be administered with caution or avoided in patients with AGS because of their high potential to activate basophils indicating a risk for anaphylaxis.”
The Jimmy Dore Show presented that there is a new patented FDA approved genetically modified breed of pig called GalSafe pigs, which are modified to eliminate alpha-gal so those suffering from AGS can still eat pork.
The pPL657 rDNA construct which integrated into the genome consisted of the DNA sequence used to disrupt the GGTA1 gene and the sequence of the neomycin phosphotransferase (nptII) gene, an antimicrobial resistance marker.
Because the nptII gene is a known antimicrobial resistance marker, it was used as a molecular biology tool during the development of the IGA.
Based on evidence from the scientific literature, information in databases of the DNA and amino acid sequences of known food allergens and toxins, and the permitted use of the nptII gene in genetically engineered plants intended for human food, FDA concluded that it is unlikely that the protein encoded by the nptII gene is a food allergen or other human food safety hazard.Source
Well, we’ll see how that one works out…..
What do you bet that this too will lead to another patentable product?
•The FDA was established in 1906 in response to public concern over unsafe food and drugs, such as spoiled food and counterfeit products. However, food industry lobbyists gradually gained influence, leading to the removal of the agency’s original leader. As a result, numerous harmful food additives were granted “generally recognized as safe” (GRAS) status and continue to be used today.
•In 1962, the FDA was given broad powers to oversee drug safety following the thalidomide incident. Unfortunately, the new regulations created strict standards for drug efficacy that were often selectively enforced, benefiting the pharmaceutical industry. Unfortunately, the FDA increasingly targeted natural therapies, which led to many being erased from history.
•Despite numerous attempts to reform the agency, issues of inefficiency and bias within the FDA persist. This article examines these challenges and suggests potential reforms to improve the agency’s role in safeguarding public health.
For most of my life, I’ve observed the FDA belligerently suppress natural treatments and any unorthodox therapy which threatens the medical monopoly while simultaneously railroading through a variety of unsafe and ineffective drugs regardless of how much public protest the agency meets.
(See link for article and videos)
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**Comment**
Please share and record this important history or it will be scrubbed and lost forever.
Like most government agencies, the FDA began well and good in the 1800’s due to unscrupulous food producers as well as medicines with secret ingredients like opium and alcohol. But, even from the get-go, the food and pharmaceutical industries were powerful and fought as lobbyists using legal tactics. The first Director of the Bureau of Chemistry, and thus the fist head of the FDA, actually resigned realizing he could do more as a private citizen than within government.
The article goes into life-saving treatments vilified by the FDA as well as ‘vaccine’ cover-ups, and disastrous drug approvals.
In a stunning admission, the allegedly neutral AMA calls for fighting for profits before care. In this article, we proposed the #RevolutionaryReform solution. Introduced for the first time ever.
In a May 2025 MedPage Todayarticle, physician and bioethicist Dr. Matthew Wynia posed the question directly: Should “no margin, no mission” apply to the AMA? His argument centers on a dilemma. According to Wynia, the AMA may wish to speak out on issues affecting scientific integrity, the welfare of vulnerable communities, and the moral conscience of the medical profession—but doing so might jeopardize the organization’s financial lifeline: its revenue from licensing the CPT (Current Procedural Terminology) code system. Speaking out could invite retaliation, he suggests, and so silence may be regrettable, but prudent.
It’s an honest and transparent claim. And it reveals a far deeper structural problem—one that goes beyond the AMA. Across American healthcare, financial entanglements have quietly reshaped institutional behavior. From lobbying agendas to billing systems to research funding, core ethical commitments are increasingly filtered through revenue considerations. Margin, once a constraint, is now a compass. (See link for article)
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SUMMARY on AMA illogic:
A false analogy is made by comparing hospitals to associations.
A false dilemma is made when the binary stay silent or risk collapse is presented.
A fallacy of eternal growth is made when revenue is presented as a right.
An appeal to consequences is made when Wynia suggests silence on federal overreach is prudent due to potential regulatory punishment
A moral inversion is given when the institution’s survival justifies passivity in the face of systemic harm.
The fallacy underpinning ‘no margin, no mission’ are reflections of deeper structural forces that shape institutional behavior constrain moral decision making and invert the very purpose of healthcare leadership.
The AMA’s economic architecture has become conflicted with the very systems it might otherwise critique. It owns and controls the Current Procedural Terminology (CPT) code system which generates tens of millions by licensing these codes to federal agencies, payers, and health IT companies. More codes equals more billing opportunities. More billing means more dependency upon AMA’s intellectual property. This is why the organization does not defend preventive, holistic, or decommodified models of care – this would reduce profits!
Regulatory Capture has become normalized in every sector of healthcare: “hospitals, medical schools, research centers, journals—have come to accept a basic bargain: to function, one must conform. To survive, one must not provoke.”
If it weren’t for independent doctors, who must completely depart from ‘consensus based medicine’ if they want patient improvement, those with Lyme/MSIDS would have no hope, no life, and no future, and would live a life of misery. These thinking doctors take on enormous risk to their practice by treating the likes of us due to the politicalization of the disease(s).
Lymeland is COVID part 1 without the red pill awakening.
A major investigation by a group of renowned German researchers has confirmed that Pfizer’s Covid mRNA “vaccines” are laced with dangerous levels of DNA contaminants.
While the presence of DNA contamination in Covid injections is not a new discovery, this latest study uses advanced techniques for more reliable quantification, making it the most significant investigation to date.
As Slay News has previously reported, leading scientists have been warning for some time that surges in deadly cancers among the Covid-vaccinated were caused by DNA fragments in the mRNA injections.
The study was led by Jürgen O. Kirchner, an Independent Researcher in Hamburg, and Professor Brigitte König of the University of Leipzig.
The results of the study were published in the Preprints journal. (See link for article)
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Important excerpt:
The researchers confirm that their findings reveal that DNA contaminations exceeded safe levels by approximately 300 to 500 times.
Kevin McKernan, a former director of the Human Genome Project, described the findings as a “bombshell.”
“Chronic activation of the cGAS-STING pathway could paradoxically fuel cancer growth,” McKernan warned.
“Repeated exposure to foreign DNA through COVID-19 boosters may amplify this risk over time, creating conditions conducive to cancer development.”
While the authors concluded that these fragments were “non-replication-competent” meaning they cannot replicate in humans, McKernan disagreed.
“To assert that the DNA fragments are non-functional, they would need to transfect mammalian cells and perform sequencing, which wasn’t done here,” McKernan stated.
“Moreover, the methods used in this study don’t effectively capture the full length of DNA fragments,” he added.
“We’re in the stage where we’re scanning through tumors to look for integration events and looking for evidence of this in cancer biopsies,” McKernan said.
“And we can find them now.
“They found one that had really high spike [protein] sent to us for sequencing.
“And we can find components of Pfizer’s vaccines inside this thing a year after vaccination.”
Hatfill is a virologist and biodefense expert, serving as a special advisor in the Administration for Strategic Preparedness and Response (ASPR) under HHS Secretary Robert F. Kennedy Jr. since early this month. He also worked in the first Trump administration who has seen the cover-ups firsthand, and he’s calling out the mRNA vaccines for what they are: a dangerous experiment.
The interview focuses on the mRNA shots causing cancer. You can tell Parish is having a hard time accepting that the ‘vaccine,’ vs the virus, is what is behind the explosion in cancer as it is my understanding she took the jab herself as many well-known Lyme literate doctors unfortunately promoted the hastily made experimental gene therapy injections. (I could be wrong on this but I feel I read it somewhere) She also is a proponent of ‘Long COVID’ despite the unfortunate truth that the shot itself is most probably behind a majority of these cases. While she wants to be non-polarizing, it’s imperative that each ‘long covid’ case is monitored for ‘vaccine’ involvement to properly determine causality. Thankfully, she is reporting on the devastating effects of the shots now.
Sensational New Study Demands Urgent Re-evaluation of mRNA Vaccines
Immunodeficiency, excess deaths, and Japan’s dangerous replicon experiment.
May 14, 2025
A groundbreaking commentary published in Discover Medicine has exposed critical flaws in global vaccination programs, particularly concerning mRNA COVID-19 vaccines and their long-term immunological consequences. The peer-reviewed, open-access study (Yamamoto, 2025) highlights alarming trends:
Vaccine-induced immunodeficiency is linked to repeated mRNA dosing
Japan is the only country still aggressively promoting boosters—including self-amplifying RNA (replicon) vaccines
Excess deaths now surpass 600,000 in Japan post-vaccination, with no clear explanation beyond aging demographics
Three infant deaths within 24 hours of routine vaccination have been dismissed as “unable to evaluate” by regulators
Here’s what you need to know about Yamamoto’s findings and their urgent implications for public health policy.
Key points
1. mRNA vaccines cause immune dysfunction
Yamamoto notes research showing three key ways that mRNA vaccines screw up immune systems:
IgG4 antibody class switching. Repeated mRNA vaccination shifts immune responses toward non-inflammatory IgG4 antibodies, potentially blunting protection against infections (Irrgang et al., 2023).
Lymphocyte depletion. Studies report post-vaccination lymphopenia (Seban et al., 2022), raising concerns about temporary immunosuppression.
Vaccine-Acquired Immunodeficiency Syndrome (VAIDS). Some researchers warn that frequent boosters may erode natural immunity (Seneff et al., 2022).
2. Japan is taking more risks on this genetic tech than other nations
While most nations halted mRNA boosters by mid-2022 due to safety concerns, Japan continues administering 8th doses, including:
Self-amplifying mRNA (saRNA) vaccines—untested in humans until now.
Simultaneous administration with flu shots, obscuring adverse event causality.
Regulatory capture: vaccine review committees include pharma-funded members, while autopsy-confirmed deaths post-vaccination are routinely classified as “unable to evaluate” (γ).
3. Baby deaths and injuries are going unacknowledged
Yamamoto notes that three infants died within 24 hours of routine vaccinations.
While autopsies were performed, no causal link was officially acknowledged. This is symptomatic of a wider systemic failure to acknowledge vaccine harms. Japan’s compensation system has historically recognized 150+ vaccine-related deaths—but none from COVID-19 vaccines, despite 932 reported fatalities.
4. Japan’s excess mortality and hidden data
Some interesting observations from Yamamoto here:
The 600,000+ excess deaths in Japan since 2021 cannot be explained by COVID-19 alone.
Similar trends have been observed in highly vaccinated Western nations (Mostert et al., 2024).
Japan’s Ministry of Health (MHLW) misclassified vaccinated individuals as “unvaccinated” in early statistics, skewing efficacy data.
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**Comment**
Despite this information and a plethora of research now showing how dangerous the ineffective shots are, the new leadership supposedly in charge of MAHA (Make America Healthy Again) flip flop more than a waffle maker. The FDA will meet on May 22, 2025 to discuss and make recommendations on the selection of the 2025-2026 formula for COVID gene therapy injections for use in the U.S.
MAHA FDA Chief, Marty Makary, Flip-Flops on COVID Shots
The Jimmy Dore Show
May 11, 2025
Newly minted FDA Chief Marty Makary is sending what some would consider “mixed” signals about his support for COVID boosters and mRNA technology. During a recent TV interview Makary said he wasn’t sure whether young, healthy children should be receiving booster shots. Whereas Makary has up to this point been among the most vocal critics of the COVID vaccine. Jimmy and former HUD Assistant Director Catherine Austin Fitts discuss why Makary would be changing his tune this way and whether he has been absorbed into “the box” that co-opts anti-establishment voices once they become insiders.
Even HHS Secretary Robert F. Kennedy recently supported the measles vaccine after an outbreak in Texas, despite saying in the past that US has measles outbreaks ‘every year,’ and that there are safety concerns about the live measles vaccine, saying testing was inadequate. He also raised safety concerns about the vaccine for pertussis. Just today Stanford scientists confirm a fatal case of vaccine-associated measles encephalitis in an immunocompromised child.
In this case, the vaccine measles virus hypermutated to a fatal strain that invaded the brain and killed the child.
If the child was unvaccinated, the AML would have been treated in the usual fashion, with a good chance at survival.Source
You won’t hear about this little factoid from mainstream media.
Madison Area Lyme Support Group 