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About stuartbramhall

Retired child and adolescent psychiatrist and American expatriate in New Zealand. In 2002, I made the difficult decision to close my 25-year Seattle practice after 15 years of covert FBI harassment. I describe the unrelenting phone harassment, illegal break-ins and six attempts on my life in my 2010 book The Most Revolutionary Act: Memoir of an American Refugee.

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

blood supply contamination

Dr Mercola

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.

[…]

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).

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.

[…]

Via https://articles.mercola.com/sites/articles/archive/2024/05/27/blood-supply-contamination.aspx

 

Bankers’ Greed: Usury the Crime of The Ages

Richard C Cook

Many historians believe, as do I, that the happiest period of history in the Christian West was during the High Middle Ages within the towns that had grown up most notably within Germany, Italy, France, and England.

Probably the most accessible chronicle of what life was like then may be found in Chaucer’s “Canterbury Tales.”

At the centers of these towns were the Gothic cathedrals which were both spiritual and technological hubs. Characteristic of the economic life of the era was the fact that the Church had outlawed usury. This was the key to personal freedom.

The dividing line between that era and our own came into being around 1500, when the German Fugger family persuaded the Pope to begin to allow usury, a practice which quickly spread.

This practice assured that, gradually, all the wealth of society would inevitably accrue to the bankers, especially when they gained the privilege of creating paper money or book-entry credits “out of thin air” and then lending it at interest.

This was the greatest crime of the ages.

We need to remember that the Christian era began when Jesus made his last visit to Jerusalem by going to the Temple and throwing out the money lenders who had desecrated it.

The Temple symbolizes, of course, all human God-given life.

When usury became widespread after 1500, citizens gradually lost all their rights and their human sanctity when they became debtors to the money lenders and were legally mere chattel whose entire well-being, and even their lives (debtors prisons), were sacrificed to the bankers’ greed.

This was understood at the time. It’s what Shakespeare depicted in the “Merchant of Venice.” It’s what the Faust legends were about, with people now selling their souls to the devil as they ruined their fellow humans.

Now, 500 years later, the process is complete. The average person is a debt-slave, subject to regimes of endless war, subject at any time to being imprisoned for the most trivial offenses, and now worthy only of being killed off by the latest “plandemic.”

But humans would be free, so a handful of nations, led by the BRICS, are breaking away from the paradigm of slavery.

These nations are all marked by strong government-owned central banks that see their role as promoting societal welfare, not as prison-guards and propagandists who work for the bankers and other elites.

It now appears that the nations of the West controlled by the regime of usury have given up on world control and are trying merely to “secure the realm” by the ever-more perfect enslavement of their increasingly unhealthy and oppressed subject populations. Meanwhile, they push and probe around the perimeters looking for weaknesses among those nations who have said “no.”

There are indeed people in the West who seek to escape, but any organized movement is immediately crushed. Still, some few individuals may find a way…..Blessings to them.

[…]

Via https://www.vtforeignpolicy.com/2024/05/usury-the-crime-of-the-ages/

How Pashinyan Regime Uses Armenians as Guinea Pigs for Pentagon’s Bioweapons

By Drago Bosnic

[…]

In a report published by the reputable Weekly Blitz, the daily’s Chief Editor Salah Uddin Shoaib Choudhury revealed extremely disturbing details about US-run biolabs in Armenia. Citing Armenian sources, Mr Choudhury reports about a measles outbreak that’s now affecting hundreds of Armenian children. According to local media, the latest incident is a result of prime minister Nikol Pashinyan’s support for the Pentagon’s bioweapons program in Armenia. For the United States, the unfortunate country is nothing but yet another pool of guinea pigs and it was precisely Pashinyan who enabled Washington DC’s exploitation of the Armenian people. As a result, they are now exposed to an unprecedented public health hazard. Armenia is just one of a string of nations affected by America’s incessant aggression against the world.

Neighboring Georgia has also been subjected to the Pentagon’s bioweapons testing. The mainstream propaganda machine has been trying to suppress reports about this, targeting globally respected journalists such as Dilyana Gaytandzhieva. Her revelations about the disturbing consequences of Washington DC’s biowarfare were far too “inconvenient” for the European Union, so Bulgaria’s most prominent investigative journalist was expelled from the troubled bloc’s parliament back in 2018 after she “dared” to confront the US Assistant Secretary of Health over hundreds of US-run biolabs in 25 countries around the world. Africa is particularly affected by this, as the US military is conducting all sorts of experiments in most countries on the continent. Worse yet, access to these biolabs is restricted even for the hosts.

American officials themselves don’t even bother denying the existence of these bioweapons facilities, although they usually resort to euphemisms when talking about it. For instance, Victoria Nuland, one of the most prominent war criminals in Washington DC, likes to use terms such as “biological research facilities”when talking about the ones found in Ukraine. One of the many reasons why Russia launched its special military operation (SMO) is precisely the existence of these biolabs where US services are building bioweapons for attacks on the Russian people. It’s hardly surprising that the Pentagon would want such facilities in Armenia. However, what’s truly disturbing is that the Pashinyan regime is ready to expose the Armenian people to such hazard, particularly in an attempt to hurt Moscow, Yerevan’s main historical ally.

Armenian media outlets report that the epidemiological situation in the country has deteriorated drastically due to American involvement. At least 786 people have been infected as a result of the measles outbreak. The Pashinyan regime refuses to disclose any information about this controversy. Informed Armenians are extremely concerned for their safety, as following the Soros-funded coup in 2018, at least 12 biolabs have been established and expanded in the South Caucasus country, all staffed by personnel sent by the Pentagon. It should be noted that most of these bioweapons facilities are located in the vicinity of residential areas and schools. Worse yet, earlier this year, Pashinyan’s Defense Minister Suren Papikyan signed an agreement with the US to establish another biolab in Gyumri.

It’s important to note that the 102nd Russian military base with 4000 soldiers is located precisely in Gyumri, which perfectly explains why the Pentagon is interested in establishing its presence there. It’s rather peculiar that Pashinyan dislikes the fact that the Russian military is in Armenia, so his government is working toward removing the base, although it’s the sole reason why the country has never been invaded by NATO member Turkey. At the same time, he wants to establish yet another American bioweapons facility that can cause a deadly epidemic not just in Armenia, but also elsewhere in the region and possibly beyond. The involvement of the Pentagon’s Defense Threat Reduction Agency (DTRA) is particularly concerning, as it deals with deadly biological materials that can be easily used as bioweapons.

The agreement between the US and the Pashinyan regime also includes the latter’s commitment to “jointly research” extremely hazardous pathogens and diseases that are not common in Armenia, including Ebola, monkeypox, the Marburg virus, Eastern equine encephalitis, as well as various types of the coronavirus. Expectedly, just like in Ukraine, Georgia, Africa and elsewhere, access to these biolabs will be limited to personnel authorized by the Pentagon. The Russian military has been warning about American bioweapons programs for years. In January this year, its Nuclear, Biological and Chemical (NBC) Protection Troops revealed the massive scope of these illegal programs, as well as the horrifying consequences of US biowarfare in Ukraine and other countries. Unfortunately, war criminals at the Pentagon managed to hijack yet another country and expand their aggression against the world.

[…]

Via https://www.globalresearch.ca/pashinyan-armenians-guinea-pigs-pentagon-bioweapons/5857908

Died Suddenly: 60 COVID-19 mRNA Vaccinated Nurses From Around the World

Image

Dr William Makis

March 7, 2024 (above) – 39 year old Christine Marie Persson, nurse at Beaumont Wayne in Michigan, died on March 7, 2024 after being intubated for 2 months. ER nurse, nursing supervisor and now an ICU nurse, she fell ill, and ended up on a ventilator.

There aren’t many details available other than this: “Christy started feeling ill months ago and has been unable to work due to multiple doctor’s appointments, hospital admissions and dozes of tests. She was just starting to feel better, had finally returned to work and suddenly took a turn for the worse. She is now on a ventilator and fighting for her life in the very ICU where she takes such amazing care of her patients.” “she has had 8 surgeries.” “After a very courageous fight the past 2 months, Christine passed away peacefully on 3/7/24”

*

COVID-19 mRNA Vaccine mandates continue to kill nurses by the hundreds. Here are 60 recent cases.

May 13, 2024 – James Ryan Hansen, died on May 13, 2024. James was only 52 years old. He was a dedicated nurse.

 

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May 8, 2024 – Louisiana – 45 year old nurse Gilbert Lashawn Fontenette died suddenly at his home on May 8, 2024.

 

 

May.2, 2024 – Windsor, ON, Canada – 22 year old Hannah Pare – Dedicated Nurse at WRH Ouellette Campus on the Neurology Floor, died due to complications following ‘routine’ surgery in Toronto to treat Audible Tinnitus.

May 2024 – UK Nurse Jody Gillie died suddenly in May 2024.

April 25, 2024 – Ohio: Registered Nurse, Kimberly Curry, 48, died April 25, 2024. She was diagnosed with Stage 2 triple negative breast cancer following her COVID Jabs.

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Apr. 18, 2024 – Australia – 38 year old Luke Lynch, singer, comedic theatre actor and veterinary nurse who cared deeply for animals died suddenly.

Apr. 5, 2024 – AUSTRALIAN NURSE DEAD – 58 year old Australian nurse from Palm Beach, Colleen Hunter died suddenly in her sleep on April 5, 2024.

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Mar. 29, 2024 – Manchester, UK – 35 year old Nurse Joanne Kelly presented with a cough and was found to have extensive bone metastases from an unknown primary cancer, only has weeks to live.

Mar. 28, 2024 – Bloomfield, NE – 32 year old Breanna Stanley, a Certified Nurse’s Assistant, died unexpectedly on March 28, 2024 from a pulmonary embolism.

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Mar. 25, 2024 – Cranbrook, BC BC and Alberta nurse 51 year old Renee Nadine Melenka Sauer died suddenly on March 25, 2024 from a brain aneurysm.

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Mar. 20, 2024 – Jerusalem, AR – Nurse Lisa Hassell died on March 20, 2024 after a battle with cancer. She was extremely excited to get COVID-19 mRNA Vaccines.

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Mar. 19, 2024 – Karen Houghton, Celebrity Kris Jenner’s younger sister who was a nurse, died suddenly from sudden cardiac arrhythmia and cardiac arrest

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Mar. 19, 2024 – UK Nurse Jan Newton developed sepsis and multi-organ failure.

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Mar. 18, 2024 – CANADIAN NURSE DEAD – Stratford, Quebec 41 year old Marie-Michele Picard died suddenly March 18, 2024. She was a nurse.

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Mar. 13, 2024 – 33 year old Natasha Mae Fester, died suddenly at her home.

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Mar. 3, 2024 – 27 year old Canadian nursing graduate Granti Kissinger Yanga fell sick on March 1 and died on March 3, 2024. Lung aspiration and cardiac arrest.

[…]

Via https://www.globalresearch.ca/died-suddenly-covid-19-mrna-vaccinated-nurses/5857889

New Zealand Mainstream Media Doesn’t Ask the Questions and Ignores the Elephant

Elephant
Photo Credit – © Canva Pro Content License

NZDSOS

As adverse effects and deaths mount in the wake of the c-19 injections we take a look at two recent Herald articles, in an attempt to provoke the gritty questions which our listless mainstream media conspicuously avoid. Meanwhile, the elephant grows increasingly obese.

Yet another NZ teenager dies suddenly in his sleep, this time while on holiday.  Running around, playing, swimming, kayaking, snorkelling and being energetic and active with family during the day, he developed a bit of a cough and chest pain, then was dead the following night.  What happened?

The NZ Herald reported “local doctors suspect the cause of death was likely from blood clots.”

The Cook Islands News provided a bit more information.  His mother Mary noted:

“There was no medical history, he was a healthy boy, he was a good eater and sporty.  He had his vaccinations, and maybe that could have been a part of it, why he got blood clots.”

Why did the NZ Herald not mention his mother’s words about his vaccinations?

It is not clear whether the suggestion of death being due to blood clots came from speculation or post mortem assessment.

Blood clots can mean several things.  If blood clots cause a cough and chest pain, the most likely type of clot is a pulmonary embolus, a clot that has travelled from the deep veins of the leg to the R side of the heart and then to the lungs.  If a clot is big enough it can block a blood vessel and stop the heart from pumping.  Smaller clots that travel into parts of one lung or the other are likely to cause sharp chest pain and shortness of breath.  It is possible for small clots to be followed by a larger fatal one.

Blood clots can also form in arteries such as the coronary arteries of the heart and block the supply of blood to the heart muscle.  This could cause a tight or heavy chest pain.  If the clot does not dissipate, a heart attack occurs damaging the heart muscle.

Although not widely publicised, both these sorts of blood clots are increasingly recognised as adverse events following mRNA injections and were expected during development of the vaccines and seen in the early post marketing surveillance.

A whole other ball game – or maybe not – are the bizarre white rubbery clots found in some living patients post jab, and after death during embalming. We have written to the pathologists’ professional organisation here, and latterly to every relevant doctors’ group in Australasia. Some evidence suggests these can appear the same as ‘normal clots’ on imaging, but they are unmistakeably different to the naked eye, and examining hands. Once felt, never forgotten.  Expect scientific reports on their composition shortly. We hope they will be a game-changer.

Another cause of sudden death associated with chest pain is myocarditis.  This is an adverse effect that can follow covid vaccination and particularly affects males in their teens and twenties, often during exertion or sleep. We have posted many references and examples.

Where are the investigative journalists asking the important questions?

We hope this family asks questions and gets proper answers about the possible role of any vaccinations in causing their boy’s death.

How many more of our young people need to die before we can talk freely about the possible causes? Meantime, stop the jabs immediately (they will be ‘available’ for infants 6 months and up from May 30th). The data has gone way past a “safety signal”. It is unfathomable that any sane authority or bureaucrat would ignore the avalanche of suddenly dead, clots, heart attacks and turbo cancers in the young that our filling our MSM headlines. What will it take?

“My baby’s got the blues…”

There is a second recent article where the NZ Herald has avoided asking an obvious question.  An 18-day-old baby turned blue and needed emergency transfer to Starship’s paediatric intensive care unit where he spent more than five weeks.  He was eventually diagnosed with ‘viral myocarditis’.  The elusive and alleged virus is not named, nor speculated upon.

However, whatever caused his illness inflamed his heart “resulting in a collapse of the left ventricle” (main pumping chamber of the heart which distributes blood to the rest of the body). Needless to say, this was previously rare – and we have commented on a number of children awaiting heart transplants in recent years.

The obvious question to us is, did the mother receive covid 19 vaccinations (or any other vaccination) either prior to or during pregnancy (or possibly both), or after delivery if breast feeding?  We are aware that, incredibly, the Immunisation Advisory Centre (IMAC) and Ministry of Health are STILL advising pregnant women to receive a vaccination for covid 19 along with other (DTaP and flu*) vaccines.  Midwives, pharmacists and GPs will be required to recommend and push these.

From the current NZ Immunisation Advisory Centre (IMAC) webpage:

Recommended and funded vaccines during pregnancy.

“COVID-19 immunisation is recommended and funded for all pregnant women in New Zealand irrespective of their eligibility for publicly funded healthcare.”

“How much protection a mother’s COVID-19 antibodies may be able to provide for her baby and for how long is being studied.”

“COVID-19 immunisation can be given during any stage of pregnancy. A booster dose of COVID-19 vaccine can be given at any stage of pregnancy, from three or more months after the primary course. Comirnaty [Pfizer mRNA vaccine] is the preferred vaccine for use during pregnancy.”

In our opinion this is the most egregious medical advice and flies completely in the face of universally agreed and well proven medical principles.

We are aware, of course, that there are other causes of myocarditis besides covid (and other) vaccinations.  However, myocarditis in a newborn infant is very rare and covid vaccinations are known to cause myocarditis with vaccine compounds found in both the placenta and breast milk.  Contrary to what we were told about the injection staying the in the arm, the lipid nanoparticles are designed to take the synthetic mRNA all over the body.

It is unfortunate that the Medsafe datasheet for the Pfizer covid injection still says under section 5.2 Pharmacokinetic properties (which includes biodistribution) “Not applicable.” i.e. it is unlikely that anyone at Pfizer has studied where exactly the lipid nanoparticles take the genetic material, particularly during pregnancy. We all know the answer by now, however – everywhere, including across the placenta.

The Air Ambulance at the bottom of the cliff… 

The Herald article above has been written to support annual fundraising for the Starship air ambulance – likely as run off its blades as all the ground-based fleets seem to be since 2021.

We think it would be good to have some funding put towards examining the covid vaccine status of mothers (and fathers) of babies presenting with cardiac and other illnesses.  Research could also be done to determine whether babies of mothers vaccinated during pregnancy are producing their own spike protein.

[…]

Via https://nzdsos.com/2024/05/22/nzs-msm-doesnt-ask-the-questions-and-ignores-the-elephant/

Egyptian Mummification: The Historical Record

Anubis, Egyptian Sarcophagus (by André, CC BY-SA)

Episode 24:  Mummification: How We Know What We Know

The History of Ancient Egypt

Professor Robert Brier

Film Review

Although Egypt mummified people for 3,000 years, it was a secret profession and Egyptian embalmers left no papyri explaining how to do it. In fact, they took an oath of allegiance agreeing not to divulge their secrets nor infringe on the territory of other embalmers.* Mummification itself was a religious procedure dedicated to Anubes (the jackal-headed god). Often there was a priest present wearing Anubes mask.

In addition to two temples in Thebes illustrating the process of mummy wrapping, the Rhind Bengreal Papyri (from 9 BC) describes various wrapping rituals, as well as broadly outlining the 70-day embalming process. For the first 35 days, the corpse was placed in a dry “place of cleansing” to dehydrate. The papyri go on to describe the seven head openings (which were filled with sacred oils), the 17 mummification rituals and the 17 “body parts” (the seven head openings plus the “four” internal organs (lungs, intestines, stomach and liver*) and the arms, legs, front and back.

The Ritual of Embalming Papyrus (from first century AD) describes waiting for three to four days of mourning before placing the corpse in natron (a naturally occurring mixture of sodium carbonate decahydrate and sodium bicarbonate) to dehydrate it. It also describe filling the head with frankincense and the body cavity with myrrh.

The most information about Egyptian mummification comes from the Greek historian Herodotus (450 BC). He asserts embalmers offered a range of three prices depending on family income. He describes placing the body in natron for 35 days, drawing red cutting lines on the abdomen, and using a sharp obsidian blade to make a 2 1/2 inch incision, as wel as a hook shaped instrument to remove the brain (through the nose).


*Embalmers also sealed the tombs following burial and were paid a fee by families of the deceased to maintain them.

*These organs were preserved in separate jars, while the heart was returned to the body.

Film can be viewed free with a library card on Kanopy.

https://www.kanopy.com/en/pukeariki/watch/video/1492791/1492848

Study Reveals Vaxxed vs Unvaxxed Blood Differences

A representative segment of a Raman infrared spectrum
of a blood sample combined with a reference spectrum (translated)

Clifford E Carnicom

A study has been done to compare the blood of individuals who have received a COVID “vaccination” with those that have not.  The results indicate that significant differences exist, and these differences are anticipated and predicted to be additionally harmful to human health.  The combination of vaccination impact with that of synthetic biology transformation (CDB, nomenclature, 2014), extensively documented on this site, is especially profound.

The detailed study was conducted with the use of Raman infrared spectroscopy.  Mid infrared spectroscopy is a method of acquiring significant knowledge of the fundamental molecular structure of a sample.

Final differences were determined by comparing the top tier of redundant peaks between the two groups, for a total of 23 peaks regarded as in common.  Of the 23 peaks in the restricted tier examined, 17 peaks are coincident between the two groups and pose no further special consideration.

This paper centers on the six peaks that differ, and the implications of those differences.  These will be discussed in a general fashion only at this time.  Some additional study notes follow at the end of this paper.

Blood is not to be changed; human beings do not command the wisdom of the evolutionary process, nor of nature, nor of the Divine, as you are so inclined.  ANY change in the structure and nature of human blood is to be understood as a threat to our existence.  The warnings are no secret at this point, and they are trumpeted across the globe by those who value life.  Continue to disregard them at your own peril.

Specifically, here are the additional warnings to be given in this paper.  These represent the deviations in blood samples from Covid “vaccinated” individuals in comparison to those that have not received such:

The Short List:

1. An unexpected or altered metallic-nitrogen (iron likely) bond exists within hemoglobin.  Not expected within one sample set only.
2. Protein and carbohydrate modification (C-O bonding) . Altered protein function and cellular communication. Not expected within blood.
3. Modification of amide bonds within proteins is likely. (Hemoglobin is a protein.)
4. Protein conformation or disulfide bond alteration is indicated.
5. Changes in fatty acid or lipids indicated. Red blood cell membranes can be affected.
6. Modification of aromatic rings possible, no single well defined functional groups in this region.

The primary combined net effect of these deviations in blood within the VAXXED sample points to alterations in hemoglobin structure that likely impact oxygen transport across the body.  Protein functioning and enzymatic activity are also likely to be impaired. This summary statement does not include the impact of the CDB (i.e., synthetic biology) upon blood and it is restricted to the spectral deviations observed.  Additional comments regarding the spectral deviations in combination with synthetic biology (CDB) impact will be discussed later.

[…]

Via https://carnicominstitute.substack.com/p/vaxxed-vs-unvaxxed-blood-differences

And the Cancer Keeps Rolling In

Todd Hayden

Kate Middleton has cancer. The King of England has cancer. Every day we hear of more and more people diagnosed with cancer—many of them quite young. And not a single report we hear, unless coming from alt media, will suggest that the Covid vaccines are a possible cause.

There is no guarantee that any particular case is definitely attributed to the jabs. But considering the radical upswing of cases recently, you would think more people would be scratching their heads and connecting the dots. The rise in cancer cases pretty clearly correlates with the release of the vaccine.

That alone should get most thinking folks questioning. But they aren’t, and they won’t.

It is much easier to blame the usual suspects—pollution, bad water, unhealthy food, toxins in general, messy lifestyles, no exercise, and now, of course, climate change. Not only is the Covid vaccine not a suspect, but no vaccine is. In fact, no FDA-approved medication is. Big Pharma can once again hold the bloody dagger behind their back with a big grin on their face, “What, me worry?” Nope, you’ve played the game well Mr. Big Pharma, you’ve got us all (or most) under your spell. No matter how obvious your implication may be, you are off the hook.

If you believe in data from mainstream sources, they tell you that in 2019, one in ten deaths worldwide was caused by cancer. Over 10 million people in that year succumbed to the dreaded “C” word. I would be curious to know what the number was in 2023, the official figures for 2022 were not much different from 2019, which indicates to me that none of these statistics can really be trusted. Most mainstream reports are not reluctant to say cancer diagnoses are on the rise, but they say that every year, and of course the incentive is to frighten people into early diagnosis and early treatment, thus filling the coffers with even more gold coins.

Oooo, did that hit a nerve? As with most confusing things these days, this is confusing. There is no doubt in my mind that some cancers, at some stages, can be successfully treated through conventional methods. How they treat these cases in the conventional world may not be as safe as how they treat them in the alternative world, but nonetheless, there have been successful treatments using conventional methods.

Of course, that conventional world will do everything it can to convince you that their interventions are the only ones that can be effective and that anything the “safe” alternative world has to offer is bogus. I personally do not believe this, but I have to say, I have not experienced alternative treatments saving many lives. And I have experienced conventional, extremely invasive, treatments doing just that, saving lives. So, what can I say? This is from personal experience, and I have had a bit of it, considering my first wife died of cancer 20 years ago.

I’m off on a tangent, my apologies.

So, back to the question, what is causing the uprise in cancer cases? In my humble opinion, the culprit is most definitely the Covid vaccine. Of course, I am just an observer and have no medical data to back up my personal opinion. From what I understand, however, the data is out there. It may be difficult to find, but there are many quite learned, experienced, and credentialed folks (as in MDs) out there who would support my statement with medical data.

Although I do believe the upswing in cancer diagnoses is largely attributed to the Covid vaccine, it cannot possibly be the only reason. And the vax is certainly not the only answer to the ubiquitous cancer diagnosis question, “Why did this happen to me?”

As we all know, the agenda has more than one way to skin a cat. mRNA in injections is only one of them. mRNA is showing up everywhere anyway, not just in needles, and in nearly every form of bodily intake. So the mRNA method can get us, even if we avoided the jab. There are known cancer-causing elements in places other than mRNA and gene therapy as well. How about 5G, Chemtrails, GMO products, cricket meal, fluoride, any number of approved pharmaceuticals, need I go on?

As they add to their wicked mix of lethal concoctions, the cancer rate just continues to climb. And there is no way to put the proverbial finger on any one thing as “the” cause.

So, we all know this. When I say, “we all” I mean those of you reading this. No one would have gotten this far in this essay if they were not already in the choir I am preaching to. We are again left with the sheep, who will probably never “get it.” Here goes the broken record skipping back into the same groove over and over again. If people, I mean sheep, actually could accurately identify the enemy and stop chasing ghosts like climate change into the woods, guaranteed never to catch them, we would possibly have a fighting chance.

I have read at least a half dozen articles, some of them even a bit alternative, about the rise in cancer cases, particularly among young people, and not a single one mentioned the Covid vaccine as a cause. Yes, all of us have been hearing since day one about the proliferation of “turbo cancer” among the vaxxed, but no one else seems to make the connection. Of course, the horse is out of the barn to some degree with all this, at least for the folks already pin-cushioned by multiple needles. It is still a battle worth fighting considering the continuation of the vaccine as a “reasonable deterrent” against Covid, for adults, the elderly, and for children. It does seem to me that it is not worth getting cancer to avoid getting Covid.

And, as you know, I am only speaking of cancer as a side effect of the vaccine, what about heart disease, blood clots, and a myriad of other known Covid vaccine side effects? And that is only to mention the ailments we have scientific support for. What about the loss of cognition, loss of empathy, depression, and suicide, along with a plethora of other mental and physical maladies that are at the moment only speculations and anecdotal observations?

[…]

Via https://off-guardian.org/2024/05/25/and-the-cancer-keeps-rolling-in/

Failing EV industry lesson to businesses; never underestimate power of consumers

Ross Clark

In China, electric vehicles have been assigned to vast graveyards of unsold vehicles. While ride-share services bought the vehicles at subsidised prices, private buyers are not so keen.  So last year China began dumping its electric vehicles in Europe, where they are filling up the ports at Rotterdam and Antwerp.

The US also has unsold stocks of electric cars.  And in Britain, the momentum for electric vehicles has slowed.

The great electric revolution that was promised just three years ago is already failing – and it will bring the car manufacturers down with it.

China is often characterised as a copycat when it comes to industry and technology but in one way it has proved to be a pioneer. It was China which saw the first boom in electric cars – and it was China that was the first to suffer when demand for them collapsed. The vast graveyards of unsold vehicles found in Hangzhou and other Chinese cities are the result of a huge, subsidised push to manufacture electric vehicles, demand for which has never caught up with supply. Ride-share services bought the vehicles – in a rerun of the great cycle-share fiasco of 2018, which led to piles of unused and unwanted bikes. But private buyers have been notably less keen.

Where China leads, the rest of the world seems doomed to follow. With China’s manufacturers struggling to sell their electric cars at home, last year they started shipping them in large numbers to Europe – where many are now accumulating in ports at Rotterdam and Antwerp. The window in which to sell them may prove small, as the EU is considering measures to prevent the ‘dumping’ of cheap Chinese cars in Europe. The Biden administration has already taken action, increasing tariffs on cars imported from China from 25 per cent to 100 per cent. While that may put paid to Chinese imports, it won’t do anything to alleviate unsold stocks of US-made electric cars. The great electric revolution that was promised just three years ago is already failing – and it will bring the car manufacturers down with it.

If there ever was a real-world demonstration of the old proverb ‘you can lead a horse to water…’, it is electric cars. Elon Musk’s visionary work with Tesla panicked the old combustion engine firms, which set themselves ambitious targets to phase out petrol completely: Fiat, Ford, Jeep, Nissan and Lexus by 2030, Vauxhall by 2028, Jaguar by 2025. One of the most dramatic announcements came three years ago when Hertz declared that a quarter of its entire rental fleet would be electric by 2025. ‘The new Hertz is going to lead the way as a mobility company,’ it said. It certainly did lead the way – into headlong retreat.

At the time, Hertz signed a $4 billion deal with Tesla and announced plans to buy 175,000 EVs from General Motors. In January it went into reverse and said it would instead start selling 20,000 EVs (later raising this to 30,000). It has pledged to ‘re-invest a portion of the proceeds from the sale of EVs into the purchase of internal combustion engine vehicles.’ Its share price (down 80 per cent since the Tesla announcement) has made it a case study.

In Britain, things don’t look much better. The slowing EV momentum led Rishi Sunak to drop his target of banning new petrol car sales by 2030 and push it back to 2035. The number of electric cars sold to drivers (as opposed to companies) was falling by 20 per cent as of last month. The UK’s market for EVs is being propped up by fleet companies which, spurred on by government incentives, now buy five in every six EVs sold.

‘Urgent action is needed to re-enthuse private buyers into switching,’ said the UK Society of Motor Manufacturers and Traders (SMMT) in its last update. It pointed out it’s not just driver demand that is flat: the infrastructure is an issue. The ratio of charging points to EV drivers has not improved since last year. The cost of electricity from a rapid charger is up by about 10 per cent, according to the RAC. So not only are EVs themselves 40 per cent more expensive to buy than petrol cars, but they are also costlier to run. The average charge for refuelling at a rapid charger is 22p per mile, compared with 17p for petrol.

Even those figures don’t really provide a fair comparison. Around half the price of a litre of petrol is tax; the tax on electricity is just 20 per cent (in the form of VAT) or 5 per cent if you charge at home. Nevertheless petrol remains cheaper. But the government is not going to sit by and watch as £25 billion of revenue from fuel duty disappears – which will happen if electric cars do take over from petrol. So at some point it is going to devise some way of recouping lost fuel duty revenue, most likely through road-charging. Early adopters who bought electric cars have effectively been treated to a generous introductory offer, which is now stealthily going to be withdrawn. When electric cars come to be taxed like petrol ones, it is going to become obvious that they cost a lot more to buy and run. That is especially true if you live in one of the 30 per cent of UK households which do not have off-street parking.

Sunak drew outrage from the green lobby when he delayed what was an obviously unworkable target. But few seemed to have noticed that he had left in place an initiative called the Zero Emission Vehicle (ZEV) mandate. This came into force in January and obliges car manufacturers to ensure that 22 per cent of the vehicles they sell in Britain this year are fully electric (as opposed to hybrid). If they fail, they will have to pay a fine of £15,000 for every vehicle by which they fall short. This target ratchets up. It will rise to 28 per cent next year and go up steadily until it hits 80 per cent by 2030.

But what to do if the public are refusing to buy? In the first four months of this year, according to the SMMT, electric cars had a market share of just 15.7 per cent, hardly up on the 15.4 per cent share in the same period of last year. Unless sales soar, manufacturers are going to be facing enormous fines in just a few months’ time.

Earlier this month Carlos Tavares, the chief executive of Stellantis (the parent company of Vauxhall, Peugeot-Citroën and Fiat) warned that the ZEV had the potential to bankrupt car-makers. He complained that the ZEV had been set at ‘double the natural demand of the market.’ He said he wouldn’t be selling cars at a loss – suggesting that, if electric car sales do not pick up soon, the company might have to restrict sales of petrol and diesel cars. (It would be easier to sympathise had Stellantis not cheered on government efforts to turn the car industry fully electric by 2030.)

Petrol-car owners have reservations that may be hard to budge. Even among households which have off-street parking, only 8 per cent say that it’s likely they would buy an electric car as their main vehicle during the next five years – although 20 per cent said they would consider one as their second vehicle. Electric cars have found a niche as second cars for relatively wealthy, environmentally aware households. But the market is beginning to run out of those kinds of buyers.

This leaves Sunak with a dilemma. The US wants to repel China’s incoming electric cars, while Germany wants to welcome them and cut all tariffs (hoping Beijing will reciprocate – BMW now sells a third of its new cars in China). What will the UK do? If Sunak wants to prioritise net-zero targets and help with the cost of living, the logical thing would be to leave the ZEV in place and welcome China’s low-cost cars (made by MG and BYD). This could be billed as using Brexit powers, lowering motoring costs with other carmakers forced to compete. But this is Stellantis’s nightmare scenario. ‘If you go and cut pricing disregarding the reality of cost,’ Tavares said in January, ‘it’s a race to the bottom and that will end up with a bloodbath.’

Forcing consumers to pay over the odds for cars would lead to an electoral bloodbath, however – which is why, unless there is a sudden rush of interest in electric cars over the next few months, the government is likely to yield. The ZEV will probably be relaxed, just as the 2030 target was relaxed last year, which will mean yet another watering-down of net-zero promises, possibly just before the election. The price will be more outrage from environmentalists, and inevitable legal challenges. Last time Sunak relaxed net-zero measures, the former minister Chris Skidmore resigned his seat and triggered a by-election.

Could the outlook suddenly improve for British EVs? It’s hard to see how. The biggest single cost is batteries, and China has built up a dominant position in the global market. About 80 per cent of EV batteries are made in China, and the West’s efforts to catch up often end in debacle. The Britishvolt factory in Northumberland went bust before its foundations were even laid. But the situation is even worse when you consider that China has near-total dominance in LFP batteries, which are cheaper to produce than the lithium manganese cobalt (NMC) batteries made in Europe. They also come with fewer ethical objections as they do not require cobalt, which is often mined by child workers under terrible conditions in the Democratic Republic of the Congo.

The traditional carmakers have responded by scaling back. Aston Martin has delayed its first electric model from 2025 to 2027 because of falling demand. Bentley has deferred its all-electric deadline. Fiat was going to phase out the petrol-powered Panda in 2026, then 2027, but now that date has been pushed back to 2030. Tesla’s deliveries fell 20 per cent in the first quarter of this year and market value has halved since the 2021 peak.

Last week, Stellantis announced a deal with the Chinese electric carmaker Leapmotor, which might just help it put off the day of reckoning with the ZEV: some of Leapmotor’s cars will be sold through a Stellantis subsidiary based in Amsterdam. In reality, this won’t do much for the planet. Making electric cars is a much more carbon-intensive business than making petrol ones, with the result that they have to be driven at least 15,000 to 20,000 miles before they can be said to have emitted less carbon. Worse, Chinese-made cars are manufactured with a far dirtier mix of electricity than UK-made cars are. Three-quarters of electricity in China is still generated by fossil fuels, 55 per cent of it from especially filthy coal. The government may well tinker with the ZEV before the year is out, but it is unlikely to admit to this greater folly, that the much-heralded switch to electric cars is likely to destroy our car industry, drive up costs for motorists – and fail to cut global emissions.

[…]

Via https://expose-news.com/2024/05/25/failing-ev-industry-is-a-lesson-to-businesses/

Local Food Movement Under Attack by New EPA Rule

Cattle on a grass field on the left and EPA in a magnifying glass on the right.

Dr Mercola

A new EPA regulatory rule that will force small meat and poultry producers to invest heavily in new water filtration systems while letting industrial factory farms off the hook is an attack on the local food movement and domestic agriculture, critics say.

Story at a Glance:

  • A new U.S. Environmental Protection Agency (EPA) regulatory rule will harm local food producers by forcing small meat and poultry producers to invest heavily in new water filtration systems or face closure.
  • This rule threatens to have long-term repercussions on the food supply and benefits factory farms and multi-national beef producers by punishing small domestic producers and incentivizing imported meat and poultry products.
  • The Kansas Natural Research Coalition, American Stewards of Liberty and a myriad of smaller coalitions have denounced these rules as a departure from the EPA’s constitutional and statutory authority.
  • Federal regulators have evaded accountability in court for decades by using their interpretation of ambiguous statutes. Consumers are best served buying beef products with American Grassfed Association Certification rather than a U.S. Department of Agriculture (USDA) stamp.

A new EPA regulatory rule is an attack on the local food movement and domestic agriculture. It will force small meat and poultry products (MPP) producers to invest heavily in new water filtration systems or face closure.

The EPA moved quickly to implement new rules on wastewater generated by the domestic MPP industry. This effort to regulate wastewater was not without opposition though.

The Kansas Natural Resource Coalition (KNRC), American Stewards of Liberty and smaller coalitions argue this is an example of federal overreach. The rule incentivizes meat importation, which may force small businesses to close.

Effluent limitations guidelines and standards

Effluent limitations guidelines (ELGs) were first defined in the Clean Water Act of 1974.

These wastewater standards are developed by the EPA based on the current technological performance of treatment and control technologies. The goal was to prevent the discharge of harmful pollutants at levels that could adversely affect human health and the environment.

ELGs vary by industry, reflecting the unique characteristics and pollution profiles of different types of industrial activities. For the MPP industry, ELGs are designed to minimize the release of nutrients, pathogens and organic matter that could deplete oxygen levels in water bodies, harm aquatic life and compromise water quality.

The standards for meat and poultry producers were last updated in 2004. Currently, they apply to approximately 150 of the 5,055 MPP facilities in the U.S.

As the KNRC pointed out, “The history of EPA’s regulation of MPP effluent guidelines and standards has never extended beyond direct discharge facilities. The proposed rule seeks to significantly expand EPA regulatory reach.”

EPA rules previously covered only direct discharge facilities

EPA rules for the MPP did not previously cover direct discharge facilities. A direct discharge facility in this industry refers to a plant or operation that releases treated or untreated effluent directly into surface waters, such as rivers, lakes or estuaries.

This contrasts with indirect discharge facilities that release effluent into municipal sewage systems for further treatment before being released into the environment.

Direct discharge facilities are subject to stringent regulatory oversight because their effluents enter the water system directly, where they can have immediate impacts on water quality and aquatic ecosystems.

EPA shifts enforcement priorities away from factory farms

The new effluent guidelines represent a major change. The EPA’s proposed amendment establishes strict limitations on nitrogen and phosphorus while adding E. coli bacteria limitations for direct discharge facilities. But they have also greatly expanded the reach of their regulations.

The EPA’s proposal, at a cost of an estimated $232 million annually, is designed to reduce pollutant discharges by 100 million pounds per year. It is just part of an aggressive plan to update effluent guidelines nationwide, applying a wave of new industry-specific standards.

Waters of the United States expanded to include private sources

Most water used in meat and poultry farming is from well sources or privately owned water sources. Under the Clean Water Act, the EPA’s authority extends to the regulation of pollutants discharged into the Waters of the United States, a term that encompasses the scope of waterbodies under federal jurisdiction.

The definition of Waters of the United States has been subject to change and legal battles, which significantly impacts regulatory scope.

These waterbodies typically include major rivers, lakes and coastal waters, along with their tributaries and adjacent wetlands. Expanding EPA rules to include private water sources represents a massive expansion of federal reach.

Moreover, as the KNRC noted in their comment to the EPA, the stringent requirements under the updated ELGs for the MPP industry raise concerns among smaller producers about the financial and operational feasibility of meeting these enhanced environmental protections.

New clean water rules fast-tracked

With something as important as the expansion of federal authority over private water sources and laws that could shutter domestic meat producers in an era of inflation and supply chain issues, you should expect a period of deliberation.

The Clean Water Act Effluent Limitations Guidelines and Standards for the Meat and Poultry Products Point Source Category rule was proposed by Biden Administration regulators on Jan. 23.

The public hearings were held Jan. 24 and Jan. 31. The minimum for public comment closed on March 24 and the new rules took effect on March 25.

The EPA public comment process requires a minimum of 60 days following the publication date. Considering the initial Clean Water Act was last updated in 2004, the stakeholders impacted by these rules hardly had time to mount a defense before they took effect.13

New meat and poultry regulations, an EPA power grab?

The KNRC argues this rulemaking’s proposal to regulate indirect discharge facilities strikingly stray from constitutional and statutory grounds, threatening to upend the delicate balance of power between state and federal governments. While it took immediate effect, it is certain to face legal challenges.

The Clean Water Act was crafted by Congress with a clear intent — to keep the primary control over land and water use firmly in the hands of the states.

As KNRC noted in their comment, the U.S. Supreme Court, in Sackett v. Environmental Protection Agency et al., highlighted the dangers of stretching the Clean Water Act’s scope too far, warning it could infringe on this critical state authority.

Nitrogen and phosphorous pollution turned up by EPA field tests

In the case of MPP producers, EPA field researchers failed to find much in the way of viruses, bacteria, heavy metals or traditional toxins. What they did find were significant quantities of two nutrients — nitrogen and phosphorus.

Nitrogen and phosphorus, while essential for the growth and health of aquatic plants, are damaging in excessive quantities. For meat and poultry producers, controlling the discharge of these nutrients within acceptable EPA guidelines can pose a major challenge.

High concentrations of nutrients in bodies of water lead to eutrophication. This is a process characterized by the overgrowth of algae that depletes oxygen levels, harming fish and other aquatic species, as has happened in Florida.

This imbalance not only disrupts ecosystems but also compromises water quality, affecting the wildlife and human populations depending on these water resources.

Concerns about new EPA restrictions

Reducing pollution of public or private water sources is an admirable goal on paper. But there is more here than meets the eye. The rules list 17 species of endangered animals, setting the table for future lawsuits by environmental groups citing the Endangered Species Act to sue the EPA and private businesses.

In their comments in the federal comment register, the KNRC stated the new rules “gives priority to environmental justice goals and emphasizes ecological benefits, but the EPA jurisdiction under the Clean Water Act is not based on ecological importance or environmental justice.”

Rules are silent about greenhouse emissions and future carbon taxes

One method of reducing nitrogen and phosphorus is anaerobic wastewater treatment.

This method uses microorganisms that consume biodegradable organic compounds, reducing organic matter and biooxygen demand in wastewater. The process generates CH4 and CO2. This combination of gases, predominantly CH4, is commonly referred to as biogas.

The new guidelines are silent on the topic of future carbon taxes and the financial toll of biogas produced by newly mandated anaerobic wastewater facilities. This is especially relevant considering the new carbon credit/taxes introduced by the Biden Administration through the Commodities Credit Corporation.

States like Oregon, California and Washington have taken the lead, implementing their own Cap and Trade laws, which require businesses to buy carbon credits to keep their doors open. This marks a significant shift in how environmental regulation and corporate responsibility are approached.

BEEF Act introduced to protect local meat processors

Reps. Ron Estes (R-Kan.) and Eric Burlison (R-Mo.) introduced the Banning EPA’s Encroachment on Facilities (BEEF) Act, H.R.7079 in response to the new EPA guidelines on Jan. 26.

This law would, “Prohibit the Administrator of the Environmental Protection Agency from finalizing, implementing or enforcing certain changes to regulations regarding meat and poultry products effluent discharges and for other purposes.”

However, supporters of the bill are not optimistic about the odds of the BEEF Act ever passing out of committee and plan legal challenges to the EPAs authority.

Fall of Chevron doctrine means legal challenges are now possible

Until recently, this is where this story would end due to Chevron deference. This is a principle of administrative law that compels federal courts to defer to a federal agency’s interpretation of an ambiguous law that the agency administers unless the interpretation is unreasonable.

The Chevron deference stems from the 1984 U.S. Supreme Court case Chevron U.S.A., Inc. v. Natural Resources Defense Council, Inc. Historically, cases against new EPA rules would advance to federal court and the judge would not consider the case on its merit due to the precedent of Chevron.

Landmark 2022 SCOTUS ruling hobbled EPA

This principle significantly impacts how environmental regulations, among others, are interpreted and implemented, affecting the balance of power between the judiciary and federal agencies. Chevron deference made it nearly impossible for private businesses to sue or slow the expansion of federal regulatory power.

Chevron deference has been largely dismantled by recent Supreme Court decisions. West Virginia v. Environmental Protection Agency has put the deference into question, particularly when it concerns significant questions of economic and political impact that Congress did not clearly delegate to the agency.

This shift in judicial thinking suggests that the EPA’s new regulations on meat and poultry producers could face significant legal challenges, especially where authority under the Clean Water Act is interpreted to include broad regulatory actions that have substantial economic consequences.

Critics long argued that such expansive interpretations by the EPA need more explicit congressional approval, reflecting a judicial recalibration of the balance of power between the legislative and executive branches in environmental regulation.

Chevron deference circumvents the legislative process and consolidates power within federal agencies, raising concerns about the separation of powers and the democratic accountability of regulatory actions.

Beef Checkoff Program is another obstacle for local producers

Small beef and poultry producers are also facing other challenges to their businesses. Apart from the new EPA rules that are likely to cripple small local farms, the mandatory USDA Beef Checkoff program has also been structured to benefit the concentrated animal feeding operation, or CAFO, model.

The program requires cattle producers to pay a $1 fee per head of cattle sold. This fund pays for the marketing of beef in the U.S., including messaging contrary to the interests of small producers who adhere to more exacting standards. The American Grassfed Certification represents a far higher standard than the USDA’s Grass-fed Beef Label.

The Supreme Court denied a 2022 petition to hear a case brought by a group of Montana-based cattle producers called R-Calf, ending years of legal challenges. R-Calf contended the Beef Checkoff program was “unconstitutionally compelled subsidies of private speech.”

[…]

Via https://childrenshealthdefense.org/defender/local-food-movement-under-attack-new-epa-rule-cola/