SV40, a DNA Altering, Carcinogenic Contaminant, found in Pfizer’s COVID-19 Vaccines
The ExposéMarch 17, 2024
It’s not just the spike protein and the mRNA that are a problem. Both Pfizer and Moderna covid injections also have DNA contamination and Pfizer’s covid injection contains SV40 promoters.

Microbiologist Kevin McKernan pioneered research on testing some of the covid vaccine vials and discovered unacceptable levels of double-stranded DNA plasmids floating around. This is DNA contamination. He found the contamination in Pfizer and Moderna vials.

During an interview with Peter Sweden, Sasha Latypova said that DNA contamination is “a huge problem because this is replication competent plasmid, it can then invade human cells, it can invade the bacterial cells that live in your gut. So, they go into the bacteria they replicate there, they replicate antibiotic-resistant genes…it can cause sepsis, it can cause cancer, all sorts of issues.”

The World Council for Health (“WCH”) stated that a red line has been crossed. “DNA contamination of mRNA ‘vaccines’ poses a risk to everyone on the planet,” WCH said. “Replicable DNA, so-called plasmids, in both the monovalent and bivalent vaccines, which should not be there at all … We can only speculate how it will end, but what needs to happen today after the publication of the paper by McKernan et al (2023) is an immediate stop of the ‘covid-19 vaccine’ program.”

In Pfizer’s mRNA injection, McKernan also discovered Simian Virus 40 (“SV40”) promoters which are tied to cancer development in humans. He emphasised that the SV40 found is a viral piece, it is not the whole virus. However, it still presents a risk of driving cancer.

SV40 or Simian Virus 40 was the 40th virus found in rhesus monkey kidney cells when these cells were used to make the polio vaccine. This virus contaminated both the inactivated polio vaccine (“IPV”) and the oral or “live” polio vaccine (“OPV”) developed by Dr. Albert Sabin. When it was discovered that SV40 was an animal carcinogen that had found its way into the polio vaccines, a federal law was passed in 1961 that required that no vaccines contain this virus.

Kanekoa The Great tweeted two audio/video transcripts. One of a recent interview with McKernan explaining his discoveries and another of a Japanese professor expressing his concerns about these discoveries. We have republished these transcripts below.

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DNA Contamination and SV40 Discovered

McKernan joined Conservative Review with Daniel Horowitz on Friday to warn that there is no quality control in the manufacturing process of these vaccines. If his findings turn out to be widespread, it could portend an even greater risk for anaphylaxis, blood clotting, developing resistance to antibiotics, gene integration risk, and long-term production of spike protein within the body. You can listen to an audio of the interview on Apple podcasts HERE.

During the interview, McKernan said:

“It’s in both Moderna and Pfizer. We looked at the bivalent vaccines for both Moderna and Pfizer and only the monovalent vaccines for Pfizer because we didn’t have access to monovalent vaccines for Moderna. In all three cases, the vaccines contain double-stranded DNA contamination. If you sequence that DNA, you’ll find that it matches what looks to be an expression vector that’s used to make the RNA…

“Whenever we see DNA contamination, like from plasmids, ending up in any injectable, the first thing people think about is whether there’s any E. coli endotoxin present because that creates anaphylaxis for the injected. And, of course, your viewers and listeners are probably aware there’s a lot of anaphylaxis going on, not only on TV but in the VAERS database. You can see people get injected with this and drop. That could be the background from this E. coli process of manufacturing the DNA…

“At least on the Pfizer side of things, it has what’s known as an SV40 promoter. This is an oncogenic virus piece. It’s not the entire virus. However, the small piece is known to drive very aggressive gene expression. And the concern that people, even at the FDA, have noted in the past whenever injecting double-stranded DNA is that these things can then integrate into the genome. If you’re not careful with how you manufacture these things, and you have excess amounts of this DNA, your concern for genome integration goes up…

“If you get an SV40 promoter in front of an oncogene, you will end up with a high expression of a gene that can drive cancer, it will be a very rare event, but you don’t need many of these cells to be hit with something like this for it to take off. SV40 actually plagued, granted it was the full viral genome, not just the promoter, but this has plagued previous vaccine programs. The polio vaccine is one of them that they were concerned that this may have contributed to cancer from that vaccine. So, there’s a history of being concerned over SV40.

“Having the promoter inside some of these vectors isn’t necessary. It seems to be superfluous oversight they could have eliminated, yet it’s still there because they ran this out the door so quickly, they didn’t really have time to get rid of superfluous parts of the plasmid. So, that piece of DNA is something we really need to pay attention to. We’ve made quantitative PCR assays to hunt for this. So several researchers around the globe are now running these assays to look for how much of this DNA is floating around after people have been vaccinated.”

Further reading:

Sequencing the Pfizer monovalent mRNA vaccines also reveals dual copy 72-bp SV40 Promoter, Anandamide (Kevin McKernan), 12 April 2023
dsDNA variance in Pfizer Docs, Anandamide (Kevin McKernan), 20 May 2023
McKernan, K., Helbert, Y., Kane, L. T., & McLaughlin, S. (2023, April 10). Sequencing of bivalent Moderna and Pfizer mRNA vaccines reveals nanogram to microgram quantities of expression vector dsDNA per dose. https://doi.org/10.31219/osf.io/b9t7m
Plasmid DNA is a Known Pfizer Ingredient – NOT a Contaminant, Karen Kingston, 14 April 2023
Japanese Professor Expresses Concern

Japanese Professor Murakami of Tokyo University expressed his concerns over the alarming discovery of SV40 promoters McKernan had made. He said:

“The Pfizer vaccine has a staggering problem. I have made an amazing finding. This figure is an enlarged view of Pfizer’s vaccine sequence. As you can see, the Pfizer vaccine sequence contains part of the SV40 sequence here. This sequence is known as a promoter. Roughly speaking, the promoter causes increased expression of the gene. The problem is that the sequence is present in a well-known carcinogenic virus.

“The question is why such a sequence that is derived from a cancer virus is present in Pfizer’s vaccine. There should be absolutely no need for such a carcinogenic virus sequence in the vaccine. This sequence is totally unnecessary for producing the mRNA vaccine. It is a problem that such a sequence is solidly contained in the vaccine. This is not the only problem. If a sequence like this is present in the DNA, the DNA is easily migrated to the nucleus.

“So, it means that the DNA can easily enter the genome. This is such an alarming problem. It is essential to remove the sequence. However, Pfizer produced the vaccine without removing the sequence. That is outrageously malicious. This kind of promoter sequence is completely unnecessary for the production of the mRNA vaccine. In fact, SV40 is a promoter of cancer viruses.”


https://expose-news.com/2024/03/17/sv40-a-dna-altering-carcinogenic-contaminant-found-in-pfizers-covid-19-vaccines/

The Silent Shame of Health Institutions
J.R. Bruning
For how much longer will health policy ignore multimorbidity, that looming, giant elephant in the room, that propagates and amplifies suffering? For how much longer will the ‘trend’ of increasing diagnoses of multiple health conditions, at younger and younger ages be rendered down by government agencies to better and more efficient services, screening modalities, and drug choices?

Multimorbidity, the presence of many chronic conditions, is the silent shame of health policy.

All too often chronic conditions overlap and accumulate. From cancer, to diabetes, to digestive system diseases, to high blood pressure, to skin conditions in cascades of suffering. Heartbreakingly, these conditions commonly overlap with mental illnesses or disorders. It’s increasingly common for people to be diagnosed with multiple mental conditions, such as having anxiety and depression, or anxiety and schizophrenia.

Calls for equity tend to revolve around medical treatment, even as absurdities and injustices accrue.

Multimorbidity occurs a decade earlier in socioeconomically deprived communities. Doctors are diagnosing multimorbidity at younger and younger ages.

Treatment regimens for people with multiple conditions necessarily entail a polypharmacy approach – the prescribing of multiple medications. One condition may require multiple medications. Thus, with multimorbidity comes increased risk of adverse outcomes and polyiatrogenesis – ‘medical harm caused by medical treatments on multiple fronts simultaneously and in conjunction with one another.’

Side effects, whether short-term or patients’ concerns about long-term harm, are the main reason for non-adherence to prescribed medications.

So ‘equity’ which only implies drug treatment doesn’t involve equity at all.

Poor diets may be foundational to the Western world’s health crisis. But are governments considering this?

The antinomies are piling up.

We are amid a global epidemic of metabolic syndrome. Insulin resistance, obesity, elevated triglyceride levels and low levels of high-density lipoprotein cholesterol, and elevated blood pressure haunt the people queuing up to see doctors.

Research, from individual cases to clinical trials, consistently show that diets containing high levels of ultra-processed foods and carbohydrates amplify inflammation, oxidative stress, and insulin resistance. What researchers and scientists are also identifying, at the cellular level, in clinical and medical practice, and at the global level – is that insulin resistance, inflammation, oxidative stress, and nutrient deficiencies from poor diets not only drive metabolic illness, but mental illnesses, compounding suffering.

There is also ample evidence that the metabolic and mental health epidemic that is driving years lost due to disease, reducing productivity, and creating mayhem in personal lives – may be preventable and reversible.

Doctors generally recognise that poor diets are a problem. Ultra-processed foods are strongly associated with adult and childhood ill health. Ultra-processed foods are

‘formulations of ingredients, mostly of exclusive industrial use, typically created by series of industrial techniques and processes (hence ‘ultra-processed’).’

In the USA young people under age 19 consume on average 67% of their diet, while adults consume around 60% of their diet in ultra-processed food. Ultra-processed food contributes 60% of UK children’s calories; 42% of Australian children’s calories and over half the dietary calories for children and adolescents in Canada. In New Zealand in 2009-2010, ultra-processed foods contributed to the 45% (12 months), 42% (24 months), and 51% (60 months) of energy intake to the diets of children.

All too frequently, doctors are diagnosing both metabolic and mental illnesses.

What may be predictable is that a person is likely to develop insulin resistance, inflammation, oxidative stress, and nutrient deficiencies from chronic exposure to ultra-processed food. How this will manifest in a disease or syndrome condition is reflective of a human equivalent of quantum entanglement.

Cascades, feedback loops, and other interdependencies often leave doctors and patients bouncing from one condition to another, and managing medicine side effects and drug-drug relationships as they go.

In New Zealand it is more common to have multiple conditions than a single condition. The costs of having two NCDs simultaneously is typically superadditive and ‘more so for younger adults.’

This information is outside the ‘work programme’ of the top echelons in the Ministry of Health:

Official Information Act (OIA) requests confirm that the Ministries’ Directors General who are responsible for setting policy and long-term strategy aren’t considering these issues. The problem of multimorbidity and the overlapping, entangled relationship with ultra-processed food is outside of the scope of the work programme of the top directorates in our health agency.

New Zealand’s Ministry of Health’s top deputy directors general might be earning a quarter of a million dollars each, but they are ignorant of the relationship of dietary nutrition and mental health. Nor are they seemingly aware of the extent of multimorbidity and the overlap between metabolic and mental illnesses.

Neither the Public Health Agency Deputy Director-General – Dr Andrew Old, nor the Deputy Director-General Evidence, Research and Innovation, Dean Rutherford, nor the Deputy Director-General of Strategy Policy and Legislation, Maree Roberts, nor the Clinical, Community and Mental Health Deputy Director-General Robyn Shearer have been briefed on these relationships.

If they’re not being briefed, policy won’t be developed to address dietary nutrition. Diet will be lower-order.

The OIA request revealed that New Zealand’s Ministry of Health ‘does not widely use the metabolic syndrome classification.’ When I asked ‘How do you classify, or what term do you use to classify the cluster of symptoms characterised by central obesity, dyslipidemia, hypertension, and insulin resistance?’, they responded:

‘The conditions referred to are considered either on their own or as part of a broader cardiovascular disease risk calculation.’

This is interesting. What if governments should be calculating insulin resistance first, in order to then calculate a broader cardiovascular risk? What if insulin resistance, inflammation, and oxidative stress are appearing at younger and younger ages, and ultra-processed food is the major driver?

Pre-diabetes and Type 2 diabetes are driven by too much blood glucose. Type 1 diabetics can’t make insulin, while Type 2 diabetics can’t make enough to compensate for their dietary intake of carbohydrates. One of insulin’s (many) jobs is to tuck away that blood glucose into cells (as fat) but when there are too many dietary carbohydrates pumping up blood glucose, the body can’t keep up. New Zealand practitioners use the HbA1c blood test, which measures the average blood glucose level over the past 2-3 months. In New Zealand, doctors diagnose pre-diabetes if HbA1c levels are 41-49 nmol/mol, and diabetes at levels of 50 nmol/mol and above.

Type 2 diabetes management guidelines recommend that sugar intake should be reduced, while people should aim for consistent carbohydrates across the day. The New Zealand government does not recommend paleo or low-carbohydrate diets.

If you have diabetes you are twice as likely to have heart disease or a stroke, and at a younger age. Prediabetes, which apparently 20% of Kiwis have, is also high-risk due to, as the Ministry of Health states: ‘increased risk of macrovascular complications and early death.’

The question might become – should we be looking at insulin levels, to more sensitively gauge risk at an early stage?

Without more sensitive screens at younger ages these opportunities to repivot to avoid chronic disease are likely to be missed. Currently, Ministry of Health policies are unlikely to justify the funding of tests for insulin resistance by using three simple blood tests: fasting insulin, fasting lipids (cholesterol and triglycerides), and fasting glucose – to estimate where children, young people, and adults stand on the insulin resistance spectrum when other diagnoses pop up.

Yet insulin plays a powerful role in brain health.

Insulin supports neurotransmitter function and brain energy, directly impacting mood and behaviours. Insulin resistance might arrive before mental illness. Harvard-based psychiatrist Chris Palmer recounts in the book Brain Energy, a large 15,000-participant study of young people from age 0-24:

‘Children who had persistently high insulin levels (a sign of insulin resistance) beginning at age nine were five times more likely to be at risk for psychosis, meaning they were showing at least some worrisome signs, and they were three times for likely to already be diagnosed with bipolar disorder or schizophrenia by the time they turned twenty-four. This study clearly demonstrated that insulin resistance comes first, then psychosis.’

Psychiatrist Georgia Ede suggests that high blood glucose and high insulin levels act like a ‘deadly one-two punch’ for the brain, triggering waves of inflammation and oxidative stress. The blood-brain barrier becomes increasingly resistant to chronic high insulin levels. Even though the body might have higher blood insulin, the same may not be true for the brain. As Ede maintains, ‘cells deprived of adequate insulin ‘sputter and struggle to maintain normal operations.’

Looking at the relationship between brain health and high blood glucose and high insulin simply might not be on the programme for strategists looking at long-term planning.

Nor are Directors General in a position to assess the role of food addiction. Ultra-processed food has addictive qualities designed into the product formulations. Food addiction is increasingly recognised as pervasive and difficult to manage as any substance addiction.

But how many children and young people have insulin resistance and are showing markers for inflammation and oxidative stress – in the body and in the brain? To what extent do young people have both insulin resistance and depression resistance or ADHD or bipolar disorder?

This kind of thinking is completely outside the work programme. But insulin levels, inflammation, and oxidative stress may not only be driving chronic illness – but driving the global mental health tsunami.

Metabolic disorders are involved in complex pathways and feedback loops across body systems, and doctors learn this at medical school. Patterns and relationships between hormones, the brain, the gastrointestinal system, kidneys, and liver; as well as problems with joints and bone health, autoimmunity, nerves, and sensory conditions evolve from and revolve around metabolic health.

Nutrition and diet are downplayed in medical school. What doctors don’t learn so much – the cognitive dissonance that they must accept throughout their training – is that metabolic health is commonly (except for some instances) shaped by the quality of dietary nutrition. The aetiology of a given condition can be very different, while the evidence that common chronic and mental illnesses are accompanied by oxidative stress, inflammation, and insulin resistance are primarily driven by diet – is growing stronger and stronger.

But without recognising the overlapping relationships, policy to support healthy diets will remain limp.

What we witness are notions of equity that support pharmaceutical delivery – not health delivery.

What also inevitably happens is that ‘equity’ focuses on medical treatment. When the Ministry of Health prefers to atomise the different conditions or associate them with heart disease – they become single conditions to treat with single drugs. They’re lots of small problems, not one big problem, and insulin resistance is downplayed.

But just as insulin resistance, inflammation, and oxidative stress send cascading impacts across body systems, systemic ignorance sends cascading effects across government departments tasked with ‘improving, promoting, and protecting health.’

It’s an injustice. The literature solidly points to lower socio-economic status driving much poorer diets and increased exposures to ultra-processed food, but the treatments exclusively involve drugs and therapy.

Briefings to Incoming Ministers with the election of new Governments show how ignorance cascades across responsible authorities.

Health New Zealand, Te Whatu Ora’s November 2023 Briefing to the new government outlined the agency’s obligations. However, the ‘health’ targets are medical, and the agency’s focus is on infrastructure, staff, and servicing. The promotion of health, and health equity, which can only be addressed by addressing the determinants of health, is not addressed.

The Māori Health Authority and Health New Zealand Joint Briefing to the Incoming Minister for Mental Health does not address the role of diet and nutrition as a driver of mental illness and disorder in New Zealand. The issue of multimorbidity, the related problem of commensurate metabolic illness, and diet as a driver is outside scope. When the Briefing states that it is important to address the ‘social, cultural, environmental and economic determinants of mental health,’ without any sound policy footing, real movement to address diet will not happen, or will only happen ad hoc.

The Mental Health and Wellbeing Commission, Te Hiringa Mahara’s November 2023 Briefing to Incoming Ministers that went to the Ministers for Health and Mental Health might use the term ‘well-being’ over 120 times – but was silent on the related and overlapping drivers of mental illness which include metabolic or multimorbidity, nutrition, or diet.

Five years earlier, He Ara Ora, New Zealand’s 2018 Mental Health and Addiction enquiry had recognised that tāngata whaiora, people seeking wellness, or service users, also tend to have multiple health conditions. The enquiry recommended that a whole of government approach to well-being, prevention, and social determinants was required. Vague nods were made to diet and nutrition, but this was not sufficiently emphasised as to be a priority.

He Ara Ora was followed by 2020 Long-term pathway to mental well-being viewed nutrition as being one of a range of factors. No policy framework strategically prioritised diet, nutrition, and healthy food. No governmental obligation or commitment was built into policy to improve access to healthy food or nutrition education.

Understanding the science, the relationships, and the drivers of the global epidemic, is ‘outside the work programmes’ of New Zealand’s Ministry of Health and outside the scope of all the related authorities. There is an extraordinary amount of data in the scientific literature, so many case studies, cohort studies, and clinical trials. Popular books are being written, however government agencies remain ignorant.

In the meantime, doctors must deal with the suffering in front of them without an adequate toolkit.

Doctors and pharmacists are faced with a Hobson’s choice of managing multiple chronic conditions and complex drug cocktails, in patients at younger and younger ages. Ultimately, they are treating a patient whom they recognise will only become sicker, cost the health system more, and suffer more.

Currently there is little support for New Zealand medical doctors (known as general practitioners, or GPs) in changing practices and recommendations to support non-pharmaceutical drug treatment approaches. Their medical education does not equip them to recognise the extent to which multiple co-existing conditions may be alleviated or reversed. Doctors are paid to prescribe, to inject, and to screen, not to ameliorate or reverse disease and lessen prescribing. The prescribing of nutrients is discouraged and as doctors do not have nutritional training, they hesitate to prescribe nutrients.

Many do not want to risk going outside treatment guidelines. Recent surges in protocols and guidelines for medical doctors reduce flexibility and narrow treatment choices for doctors. If they were to be reported to the Medical Council of New Zealand, they would risk losing their medical license. They would then be unable to practice.

Inevitably, without Ministry of Health leadership, medical doctors in New Zealand are unlikely to voluntarily prescribe non-drug modalities such as nutritional options to any meaningful extent, for fear of being reported.

Yet some doctors are proactive, such as Dr Glen Davies in Taupo, New Zealand. Some doctors are in a better ‘place’ to work to alleviate and reverse long-term conditions. They may be later in their career, with 10-20 years of research into metabolism, dietary nutrition, and patient care, and motivated to guide a patient through a personal care regime which might alleviate or reverse a patient’s suffering.

Barriers include resourcing. Doctors aren’t paid for reversing disease and taking patients off medications.

Doctors witness daily the hopelessness felt by their patients in dealing with chronic conditions in their short 15-minute consultations, and the vigilance required for dealing with adverse drug effects. Drug non-compliance is associated with adverse effects suffered by patients. Yet without wrap-around support changing treatments, even if it has potential to alleviate multiple conditions, to reduce symptoms, lower prescribing and therefore lessen side effects, is just too uncertain.

They saw what happened to disobedient doctors during Covid-19.

Given such context, what are we to do?

Have open public discussions about doctor-patient relationships and trust. Inform and overlay such conversations by drawing attention to the foundational Hippocratic Oath made by doctors, to first do no harm.

Questions can be asked. If patients were to understand that diet may be an underlying driver of multiple conditions, and a change in diet and improvement in micronutrient status might alleviate suffering – would patients be more likely to change?

Economically, if wrap-around services were provided in clinics to support dietary change, would less harm occur to patients from worsening conditions that accompany many diseases (such as Type 2 diabetes) and the ever-present problem of drug side-effects? Would education and wrap-around services in early childhood and youth delay or prevent the onset of multimorbid diagnoses?

Is it more ethical to give young people a choice of treatment? Could doctors prescribe dietary changes and multinutrients and support change with wrap-around support when children and young people are first diagnosed with a mental health condition – from the clinic, to school, to after school? If that doesn’t work, then prescribe pharmaceutical drugs.

Should children and young people be educated to appreciate the extent to which their consumption of ultra-processed food likely drives their metabolic and mental health conditions? Not just in a blithe ‘eat healthy’ fashion that patently avoids discussing addiction. Through deeper policy mechanisms, including cooking classes and nutritional biology by the implementation of nourishing, low-carbohydrate cooked school lunches.

With officials uninformed, it’s easy to see why funding for Green Prescriptions that would support dietary changes have sputtered out. It’s easy to understand why neither the Ministry of Health nor Pharmac have proactively sourced multi-nutrient treatments that improve resilience to stress and trauma for low-income young people. Why there’s no discussion on a lower side-effect risk for multinutrient treatments. Why are there no policies in the education curriculum diving into the relationship between ultra-processed food and mental and physical health? It’s not in the work programme.

There’s another surfacing dilemma.

Currently, if doctors tell their patients that there is very good evidence that their disease or syndrome could be reversed, and this information is not held as factual information by New Zealand’s Ministry of Health – do doctors risk being accused of spreading misinformation?

Government agencies have pivoted in the past 5 years to focus intensively on the problem of dis- and misinformation. New Zealand’s disinformation project states that

Disinformation is false or modified information knowingly and deliberately shared to cause harm or achieve a broader aim.
Misinformation is information that is false or misleading, though not created or shared with the direct intention of causing harm.
Unfortunately, as we see, there is no division inside the Ministry of Health that reviews the latest evidence in the scientific literature, to ensure that policy decisions correctly reflect the latest evidence.

There is no scientific agency outside the Ministry of Health that has flexibility and the capacity to undertake autonomous, long-term monitoring and research in nutrition, diet, and health. There is no independent, autonomous, public health research facility with sufficient long-term funding to translate dietary and nutritional evidence into policy, particularly if it contradicted current policy positions.

Despite excellent research being undertaken, it is highly controlled, ad hoc, and frequently short-term. Problematically, there is no resourcing for those scientists to meaningfully feedback that information to either the Ministry of Health or to Members of Parliament and government Ministers.

Dietary guidelines can become locked in, and contradictions can fail to be chewed over. Without the capacity to address errors, information can become outdated and misleading. Government agencies and elected members – from local councils all the way up to government Ministers, are dependent on being informed by the Ministry of Health, when it comes to government policy.

When it comes to complex health conditions, and alleviating and reversing metabolic or mental illness, based on different patient capacity – from socio-economic, to cultural, to social, and taking into account capacity for change, what is sound, evidence-based information and what is misinformation?

In the impasse, who can we trust?

Published under a Creative Commons Attribution 4.0 International License
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Author

J.R. Bruning is a consultant sociologist (B.Bus.Agribusiness; MA Sociology) based in New Zealand. Her work explores governance cultures, policy and the production of scientific and technical knowledge. Her Master’s thesis explored the ways science policy creates barriers to funding, stymying scientists’ efforts to explore upstream drivers of harm. Bruning is a trustee of Physicians & Scientists for Global Responsibility (PSGR.org.nz). Papers and writing can be found at TalkingRisk.NZ and at JRBruning.Substack.com and at Talking Risk on Rumble.

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The story of Yazan Kafarneh, the boy who starved to death in Gaza
Tareq S. HajjajMarch 25, 2024
Yazan Kafarneh after dying of starvation. (Photo: Rabee' Abu Naqirah)
Yazan Kafarneh after dying of starvation. (Photo: Rabee’ Abu Naqirah)
This is not a photo of a mummy or an embalmed body retrieved from one of Gaza’s ancient cemeteries. This is a photo of Yazan Kafarneh, a child who died of severe malnutrition during Israel’s genocidal war on the Gaza Strip.

Yazan’s family now lives in the Rab’a School in the Tal al-Sultan neighborhood in Rafah City. His father, Sharif Kafarneh, along with his mother, Marwa, and his three younger brothers, had fled Beit Hanoun in northern Gaza early on in the war.

Yazan Kafarneh died at the age of nine, the eldest of four brothers — Mouin, 6, Ramzi, 4, and Muhammad, born during the war in a shelter four months ago.

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Living in conditions not fit for human habitation, the grieving family had witnessed Yazan’s death before their eyes. It didn’t happen all at once but unfolded gradually over time, his frail body wasting away one day after another until there was nothing left of Yazan but skin and bones.

Sharif was unable to do anything for his son. He died due to a congenital illness that required a special dietary regimen to keep him healthy. Israel’s systematic prevention of food from reaching the civilian population in Gaza meant that severe malnutrition — suffered by most children in the besieged enclave — in the case of Yazan meant death.

“We first left from Beit Hanoun to Jabalia refugee camp,” Sharif told Mondoweiss. “Then the occupation called us again and warned us against staying where we were. So we left for Gaza City. Then, the occupation forced us to flee further south, and we did.”

Yazan Kafarneh's parents and three brothers in their shelter in Rafah. (Photo: Tareq Hajjaj/Mondoweiss)
Sharif Kafarneh’ (left), his wife Marwa (right), and their three surviving sons (center) in their shelter in Rafah. (Photo: Tareq Hajjaj/Mondoweiss)
“If it weren’t for Yazan, I would have never left my home,” Sharif maintained. “Yazan required special care and nutrition.”

Yazan suffered from a congenital form of muscular atrophy that made movement and speech difficult, but Sharif said that it never caused him much grief in his nine short years before the war.

“He just had advanced nutritional needs,” Sharif explained. “But getting that food for him was never an issue before the war.”

It was a point of pride for Sharif that he, a taxi driver, had never left his child wanting or deprived.

“That changed in the war. The specific foods that he needed were cut off,” he said. “For instance, Yazan had to have milk and bananas for dinner every day. He can’t go a day without it, and sometimes he can have only bananas. This is what the doctors told us.”

“After the war, I couldn’t get a single banana,” Sharif continued. “And for lunch, he had to have boiled vegetables and fruits that were pureed in a blender. We had no electricity for the blender, and there were no fruits or vegetables anymore.”

As for breakfast, Yazan’s regimen demanded that he eat eggs. “Of course, there aren’t any more eggs in Rafah City,” Sharif said. “No fruits, no vegetables, no eggs, no bananas, nothing.”

“But our child’s needs were never a problem for us,” Sharif rushed to add. “We loved taking care of him. He was the spoiled child of the family, and his younger brothers loved him and took care of him, too. God gave me a living so I could take care of him.”

Due to his special needs, charitable societies used to visit Yazan’s home in Beit Hanoun before the war, providing various treatments such as physical therapy and speech therapy. All in all, Yazan had a functional, happy childhood.

‘He got thinner and thinner’

The family continued to take care of Yazan throughout the war. They tried to make do with what they could find, trying as much as possible to find alternatives to the foods Yazan required. “I replaced bananas with halawa [a tahini-based confection], and I replaced eggs with bread soaked in tea,” Sharif said. “But these foods did not contain the nutrients that Yazan needed.”

In addition to his nutritional needs, Yazan had specific medicines to take. Sharif used to bring him brain and muscle stimulants that helped him stay alive and mobile, allowing him to move around and crawl throughout their home. Those medicines ran out during the second week of the war.

With the lack of nutrition and medication, his health took a turn for the worse. “I noticed him getting sick, and his body was becoming emaciated,” Sharif recounts. “He got thinner and thinner.”

His family took him to al-Najjar Hospital in Rafah, where his health continued to deteriorate over the course of eleven days.

“Even after we took him to the hospital, they couldn’t do anything for him,” Sharif continued. “All they were able to give him were IV fluids, and when his situation got worse, the hospital staff placed a feeding tube in his nose.”

“My son required a tube with a 14-unit measurement, but all the hospital had was an 8-unit,” he added.

When asked what was the most important factor that led to the deterioration of his son’s condition, Sharif said that it was the environment he lived in. “Before the war, he was in the right environment. After, everything was wrong. He was in his own home, but then he was uprooted to a shelter in Rafah.”

“The situation we’re living in isn’t fit for humans, let alone a sick child,” Sharif explained. “In the camps, people would light fires to keep themselves warm, but the smoke would cause Yazan to cough and suffocate, and we weren’t able to tell them to turn their fires off because everyone was so cold.”

Dr. Muhammad al-Sabe’, a pediatric surgeon in Rafah who works at the al-Awda, al-Najjar, and al-Kuwaiti hospitals, took a special interest in Yazan’s case.

“The harsh conditions Yazan had to endure, including malnutrition, were the main factors contributing to the deterioration of his health and his ultimate death,” Dr. al-Sabe’ told Mondoweiss. “This is a genetic and congenital illness, and it requires special care every day, including specific proteins, IV medicines, and daily physical therapy, which isn’t available at Rafah.”

“If things don’t change, if they stay the way they are, we’re going to witness mass death among children.”
Dr. Muhammad al-Sabe’normal
Dr. al-Sabe’ said that most foods administered to patients who cannot feed themselves through feeding tubes are unavailable in Gaza. “The occupation prevents these specific foods and medicines from coming in,” he explained. “Including a medicine called Ensure.”

Ensure is a special nutritional supplement used in medical settings for what is called “enteral nutrition” — feeding patients through a nasal tube.

“Special treatment for patients, especially children, is nonexistent,” Dr. al-Sabe’ added. “We don’t even have diapers, let alone baby formula and nutritional supplements.”

“If things don’t change, if they stay the way they are, we’re going to witness mass death among children,” he stressed. “If any child doesn’t receive nutrition for an entire week, that child will eventually die. And even if malnourished children are eventually provided with nutrition, they will likely suffer lifelong health consequences.”

“If medicine is cut off from children who need it for one week, this will also likely lead to their death,” he continued.

Yazan Kafarneh after dying of starvation. (Photo: Rabee' Abu Naqirah)
Images of Yazan Kafarneh’s emaciated body circulated widely on social media. (Photo: Rabee’ Abu Naqirah)
Children disproportionately affected by famine

According to a UNICEF humanitarian situation report on March 22, 2.23 million people in Gaza suffer at least from “acute food insecurity,” while half of that population (1.1 million people) suffers from “catastrophic food insecurity,” meaning that “famine is imminent for half of the population.”

An earlier report in December 2023 had already concluded that all children in Gaza under five years old (estimated to be 335,000 children) are “at high risk of severe malnutrition and preventable death.” UNICEF’s most recent March 22 report estimates that the famine threshold for “acute food insecurity” has already been “far exceeded,” while it is highly likely that the famine threshold for “acute malnutrition” has also been exceeded. Moreover, UNICEF said that the Famine Review Committee predicted that famine would manifest in Gaza anywhere between March and May of this year.

Dr. al-Sabe’ stresses that such dire conditions disproportionately affect children, who have advanced nutritional needs compared to adults.

“Their bodies are weak, and they don’t have large stores of muscle and fat,” he explained. “Even one day of no food for a young child will lead to consequences that are difficult to control in the future.”

“An adult male may go a week without food before signs of malnutrition begin to show,” he continued. “Not so with children. Their muscle mass increases whenever they eat, which in turn leads to a greater need for nutrients.”

The lack of nutrients means that children will grow weak, the pediatric surgeon said, and that they will quickly begin to exhibit symptoms such as fatigue, sleepiness, diarrhea, vomiting, anemia, sunken eyes, and joint pains. For the same reason, Dr. al-Sabe maintained, children also respond to treatment fairly quickly — but “on the condition that they have not experienced malnutrition for more than a week.”

After one week, reversing the effects of malnutrition becomes much more difficult. Al-Sabe’ asserts that children’s digestive tracts will slow down, they might begin to suffer from kidney failure, and their bellies can swell with fluids.

That is what is particularly devastating for Gaza — over 335,000 children have undergone varying degrees of extreme malnutrition for months on end. The consequences are difficult to fathom on a population-wide level and for future generations. As of the time of writing, over 30 children have already died due to malnutrition in northern Gaza, but the real number is likely much higher given the lack of reporting in many areas in the north.

‘He didn’t need a miracle to save him’

Yazan’s mother, Marwa Kafarneh, could barely contain her tears as she spoke of her son.

“He was a normal boy despite his illness,” she told Mondoweiss. “He played with his brothers. He crawled and moved about, and he could open closets and use the phone, and he would watch things on it for hours.”

“He could have lived a long life, a normal life,” she continued. “His father would have brought him everything that he needed. He wouldn’t have had to feel hungry for even a single day.”

When she saw that the images of her son’s emaciated body had gone viral on social media, Marwa said that she preferred death over looking at the photos. “My eldest son died in front of my eyes, in front of all of our eyes,” she said. “We weren’t able to save him. And he didn’t need a miracle to save him either. All he needed was the food that we’ve always been able to provide for him.”

Reflecting as she cried, she added: “But finding that food in Gaza today takes nothing less than a miracle.”

Tareq S. Hajjaj
Tareq S. Hajjaj is the Mondoweiss Gaza Correspondent and a member of the Palestinian Writers Union. He studied English Literature at Al-Azhar University in Gaza. He started his career in journalism in 2015, working as a news writer and translator for the local newspaper Donia al-Watan. He has reported for Elbadi, Middle East Eye, and Al-Monitor. Follow him on Twitter at @Tareqshajjaj.

BEFORE YOU GO – At Mondoweiss, we understand the power of telling Palestinian stories. For 17 years, we have pushed back when the mainstream media published lies or echoed politicians’ hateful rhetoric. Now, Palestinian voices are more important than ever.

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https://mondoweiss.net/2024/03/the-story-of-yazan-kafarneh-the-boy-who-starved-to-death-in-gaza/

Catastrophic antiphospholipid syndrome Diagnosed 5 Days After Pfizer Covid "Vaccine"

A 35 year old woman is very sick now only 1 day after her Pfizer shot. Five days after presenting with stomach pain, vomiting and shortness of breath, she was diagnosed with antiphospholipid syndrome which is an autoimmune, hypercoagulable state caused by antiphospholipid antibodies. APS can lead to blood clots (thrombosis) in both arteries and veins, pregnancy-related complications, and other symptoms like low platelets, kidney disease, heart disease, and rash.

The woman was found to have a blood clot in her heart and had memory loss and confusion with deep brain cell death in both frontal lobes and her left parietal lobe.

Dr. McCullough responded to a case study shared on X,

"Case exemplifies why COVID-19 vaccines should not have been rolled out indiscriminately. For this 35-year old woman with antiphospholipid syndrome, COVID-19 vaccination was a disaster. She would be fine today living a normal life if she chose to be unvaccinated."

Dr. McCullough on X
Case Study

Join us
@CovidVaccineAdverseReactions

SATIRE – In an alternative universe Bill Gates has called for the withdrawal of all Covid-19 Vaccines
The ExposéAugust 29, 2021
A note from The Editor – when we first published this article we should have made it clear at the beginning that it was satire rather than at the end. We did not do this and we apologise…

However, an investigation (which is entirely factual) into the shocking ties between Mr Bill Gates, Moderna, and the U.K. Medicine Regulator has now been published with explosive revelations into the real reason the Moderna injection has been given emergency authorisation for use in children. Please read it here and share it widely.

INVESTIGATION – Bill Gates has an agreement with Moderna that grants him a license to their Covid-19 Vaccine; a vaccine that was produced weeks before the emergence of Covid-19
Thank you

Note – The following satire is fictional in that Mr. Gates has made no such speech and the Gates Foundation has not established any funds to compensate vaccine victims or to make available effective, inexpensive COVID-19 remedies. All the rest of the article is factual – W. Gelles

In a shocking announcement, Bill Gates, billionaire Microsoft co-founder and the major force behind the COVID-19 vaccines, called for all the COVID-19 genetic-based vaccines to be taken off the market immediately.

In an often anguished 19-minute televised speech, Gates said: “We made a terrible mistake. We wanted to protect people against a dangerous virus. But it turns out the virus is much less dangerous than we thought. And the vaccine is far more dangerous than anyone imagined.”

“These vaccines—Pfizer, Moderna, Johnson & Johnson, AstraZeneca—they’re killing people left and right—and they’re injuring some people very badly,” Gates continued, waving his hands in the air at times for dramatic effect.

“The government’s own data shows us this is what’s happening. The CDC’s reporting system is showing, what?…around 13,000 deaths so far in the U.S. and over half a million adverse events. Well, we all know the reporting system is a sham.

“We know that VAERS [Centers for Disease Control and Prevention’s Vaccine Adverse Events Reporting System] captures only around one percent of what’s going on. So we’re talking over a million deaths from these Covid vaccines, and more than 60 million people with bad side effects.”

“This is not what we wanted. This is not acceptable,” Mr. Gates asserted.

Wall Street shares of all the major Covid vaccine companies plummeted by 20% to 30% as Mr. Gates announced that he was joining the urgent Citizen Petition filed by Robert F. Kennedy Jr.’s Children’s Health Defense organization calling on the U.S. Food and Drug Administration to immediately withdraw all the COVID vaccines from the market.

Gates continued: “Too many people who take these vaccines drop dead…one day, two days, five days after getting the shot. Other people suffer paralysis, blindness, convulsions, heart attacks, immune system collapse, blood clots, brain inflammation, lung or kidney damage, miscarriages, autoimmune disease, multiple organ system failure, permanent profound fatigue, and many other horrible problems.

“Of course, our Media Mouthpieces—I mean the mainstream news media, dismiss all these tragedies as ‘just a coincidence.'”

“The reason they say that,” Gates explained, “is because of what I did at Event 201, a Coronavirus Pandemic Simulation held in New York in October 2019 just a few weeks before we announced the actual pandemic. I got all the major newspapers, TV channels, and radio stations to agree to stick with the Official Narrative—‘the vaccines are safe and effective’—and to censor anybody who questions this line of BS.

“So the public never got to hear the evidence from hundreds of distinguished doctors and medical researchers who warned that the vaccines are dangerous and often lethal.”

“That was a huge mistake on my part,” Gates maintained, looking weary and at times teary-eyed. “We never should have done that. People have every right to be well-informed, to get all the facts so they can make a rational decision.”

Changing the topic as if to elicit sympathy, Mr. Gates confided: “I’ve been going through a rough time and doing a lot of soul-searching since Melinda dumped me. This divorce has caused me to take a good hard look at myself. I don’t want to be remembered as a monster who killed millions of people through deadly vaccines. I am not a monster. I am not a mass murderer. I don’t want to be remembered as a mass murderer by my family, my friends, and my company.

“Some people have called me a sociopath or even a psychopath because of my visionary schemes to help humanity—like reducing global warming by spraying dust into the upper atmosphere, or releasing millions of genetically-modified mosquitoes to combat dengue and Zika virus.”

“Melinda didn’t understand my dreams. She didn’t understand my relationship with Jeffrey Epstein… It was purely a casual friendship and had nothing to do with having sex with underage girls. Jeff ran a blackmail ring for Mossad, Israel’s spy agency, and I would never be so dumb as to risk putting myself in a compromising position.”

“But getting back to these vaccines,” Mr. Gates shifted gears as he regained his composure, “These products quite frankly do not meet the legal or scientific definition of a vaccine. They’re highly experimental injections which genetically instruct a person’s body to manufacture zillions of spike proteins. The injected material travels everywhere through the bloodstream, and soon your whole body is making these damn spike proteins.

“Now, the whistleblowers were telling us for over a year that the spike protein is a pathogen—it’s toxic and it also creates blood clots and damages multiple organs. Well, it turns out they were absolutely correct. And there’s other cutting-edge science in these vaccines that also turned out to be harmful, like a magnetic ingredient which turns people into human transmitters/receivers, but I am not at liberty to discuss these issues today, under the advice of legal counsel.”

“We thought we were doing some really cool things with these Covid vaccines—‘actually hacking the software of life,’ as my good friend Tal Zaks, Moderna’s Chief Medical Officer, once boasted. But we went too far. We blew it,” Gates confessed in a rare admission of defeat.

“Basically,” the Microsoft mogul conceded, “we tricked people into taking these vaccines. There was no need for them at all, since the COVID-19 respiratory virus is less deadly than the seasonal flu—and 99.9-plus percent of people recover spontaneously from infection with this virus within a few days.

“I supported the German research group which convinced the World Health Organization to accept the PCR diagnostic test as the ‘gold standard’—when any college student knows you can’t use the PCR test to diagnose for any disease. But we ramped up the test to 35 or 40 cycles so that 95 percent of the people would get false-positives. I don’t know why I did that. Mea culpa,” Gates shrugged as he drank a glass of water.

“To sum up,” Mr. Gates said, waving his fingers in the air, “The vaccines do NOT confer immunity, they do NOT prevent transmission of the virus. They only claim to reduce mild symptoms in infected people, and they don’t do a good job of that either, despite the inflated statistics. Countless people who get the shot are later diagnosed with COVID-19 infection. Plus, there are many inexpensive, effective remedies that are widely used around the world to defeat COVID-19. There was no need for lockdowns or masks.”

“The whole thing is a farce, and I’m very, very, truly sorry,” Mr. Gates concluded as he dashed off the set without taking questions.

Shortly after his speech, the Bill & Melinda Gates Foundation announced that it is setting up a special $50 billion fund in tandem with the vaccine manufacturers to provide fair and just compensation for Covid vaccine victims and their families. The Gates Foundation also announced it has set up a separate $50 billion fund to provide free ivermectin, hydroxychloroquine, budesonide, Vitamins D, C, and B, zinc, pine needle tea, N-acetyl cysteine, and other remedies to anyone who requests these treatments.

Hydroxychloroquine is known to be very effective in fighting COVID-19, but in order for the FDA to grant “Emergency Use Authorization” to the risky “vaccines” which failed all previous clinical trials, there had to be no other effective treatments available. So the prestigious Lancet and New England Journal of Medicine published bogus research papers to discredit hydroxychloroquine. The articles, which used fabricated data, were later retracted, but by then they had accomplished their purpose and the fake vaccines were rolled out by President Donald Trump on an unsuspecting, badly informed public.

The Biden administration, which is relentlessly pushing for all Americans to get the dangerous injections, had no immediate reaction to Gates’s bombshell speech. President Biden was reportedly asleep in the basement of his private home.

Note: The above satire is fictional in that Mr. Gates has made no such speech and the Gates Foundation has not established any funds to compensate vaccine victims or to make available effective, inexpensive COVID-19 remedies. All the rest of the article is factual – W. Gelles

https://expose-news.com/2021/08/29/bill-gates-calls-for-the-withdrawal-of-all-covid-19-vaccines/


https://telegra.ph/SATIRE--In-an-alternative-universe-Bill-Gates-has-called-for-the-withdrawal-of-all-Covid-19-Vaccines-03-11

“Let Them Eat Dirt”. Israel has Given Palestinians in Gaza Two Choices. Leave or Die. Chris Hedges
The final stage of Israel’s genocide in Gaza, an orchestrated mass starvation, has begun. The international community does not intend to stop it.


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***

There was never any possibility that the Israeli government would agree to a pause in the fighting proposed by Secretary of State Antony Blinken, much less a ceasefire. Israel is on the verge of delivering the coup de grâce in its war on Palestinians in Gaza – mass starvation. When Israeli leaders use the term “absolute victory,” they mean total decimation, total elimination. The Nazis in 1942 systematically starved the 500,000 men, women and children in the Warsaw Ghetto. This is a number Israel intends to exceed.

Israel, and its chief patron the United States, by attempting to shut down the United Nations Relief and Works Agency for Palestine Refugees in the Near East (UNRWA), which provides food and aid to Gaza, is not only committing a war crime, but is in flagrant defiance of the International Court of Justice (ICJ). The court found the charges of genocide brought by South Africa, which included statements and facts gathered by UNWRA, plausible. It ordered Israel to abide by six provisional measures to prevent genocide and alleviate the humanitarian catastrophe. The fourth provisional measure calls on Israel to secure immediate and effective steps to provide humanitarian assistance and essential services in Gaza.

UNRWA’s reports on conditions in Gaza, which I covered as a reporter for seven years, and its documentation of indiscriminate Israeli attacks illustrate that, as UNRWA said, “unilaterally declared ‘safe zones’ are not safe at all. Nowhere in Gaza is safe.”

UNRWA’s role in documenting the genocide, as well as providing food and aid to the Palestinians, infuriates the Israeli government. Prime Minister Benjamin Netanyahu accused UNRWA after the ruling of providing false information to the ICJ. Already an Israeli target for decades, Israel decided that UNRWA, which supports 5.9 million Palestinian refugees across the Middle East with clinics, schools and food, had to be eliminated. Israel’s destruction of UNRWA serves a political as well as material objective.

The evidence-free Israeli accusations against UNRWA that a dozen of the 13,000 employees had links to those who carried out the attacks in Israel on Oct. 7, which saw some 1,200 Israelis killed, did the trick. It led 16 major donors, including the United States, the U.K., Germany, Italy, the Netherlands, Austria, Switzerland, Finland, Australia, Canada, Sweden, Estonia and Japan, to suspend financial support for the relief agency on which nearly every Palestinian in Gaza depends for food. Israel has killed152 UNRWA workers and damaged 147 UNRWA installations since Oct. 7. Israel has also bombed UNRWA relief trucks.

More than 27,708 Palestinians have been killed in Gaza, some 67,000 have been wounded and at least 7,000 are missing, most likely dead and buried under the rubble.

More than half a million Palestinians – one in four – are starving in Gaza, according to the U.N. Starvation will soon be ubiquitous. Palestinians in Gaza, at least 1.9 million of whom have been internally displaced, lack not only sufficient food, but clean water, shelter and medicine. There are few fruits or vegetables. There is little flour to make bread. Pasta, along with meat, cheese and eggs, have disappeared. Black market prices for dry goods such as lentils and beans have increased 25 times from pre-war prices. A bag of flour on the black market has risen from $8.00 to $200 dollars. The healthcare system in Gaza, with only three of Gaza’s 36 hospitals left partially functioning, has largely collapsed. Some 1.3 million displaced Palestinians live on the streets of the southern city of Rafah, which Israel designated a “safe zone,” but has begun to bomb. Families shiver in the winter rains under flimsy tarps amid pools of raw sewage. An estimated 90 percent of Gaza’s 2.3 million people have been driven from their homes.

“There is no instance since the Second World War in which an entire population has been reduced to extreme hunger and destitution with such speed,” writes Alex de Waal, executive director of the World Peace Foundation at Tufts University and the author of “Mass Starvation: The History and Future of Famine,” in the Guardian. “And there’s no case in which the international obligation to stop it has been so clear.”

The United States, formerly UNRWA’s largest contributor, provided $422 million to the agency in 2023. The severance of funds ensures that UNRWA food deliveries, already in very short supply because of blockages by Israel, will largely come to a halt by the end of February or the beginning of March.

Israel has given the Palestinians in Gaza two choices. Leave or die.

I covered the famine in Sudan in 1988 that took 250,000 lives. There are streaks in my lungs, scars from standing amid hundreds of Sudanese who were dying of tuberculosis. I was strong and healthy and fought off the contagion. They were weak and emaciated and did not. The international community, as in Gaza, did little to intervene.

The precursor to starvation – undernourishment – already affects most Palestinians in Gaza. Those who starve lack enough calories to sustain themselves. In desperation people begin to eat animal fodder, grass, leaves, insects, rodents, even dirt. They suffer from diarrhea and respiratory infections. They rip up tiny bits of food, often spoiled, and ration it.

Soon, lacking enough iron to produce hemoglobin, a protein in red blood cells that carries oxygen from the lungs to the body, and myoglobin, a protein that provides oxygen to muscles, coupled with a lack of vitamin B1, they become anemic. The body feeds on itself. Tissue and muscle waste away. It is impossible to regulate body temperature. Kidneys shut down. Immune systems crash. Vital organs – brain, heart, lungs, ovaries and testes — atrophy. Blood circulation slows. The volume of blood decreases. Infectious diseases such as typhoid, tuberculosis and cholera become an epidemic, killing people by the thousands.

It is impossible to concentrate. Emaciated victims succumb to mental and emotional withdrawal and apathy. They do not want to be touched or moved. The heart muscle is weakened. Victims, even at rest, are in a state of virtual heart failure. Wounds do not heal. Vision is impaired with cataracts, even among the young. Finally, wracked by convulsions and hallucinations, the heart stops. This process can last up to 40 days for an adult. Children, the elderly and the sick expire at faster rates.

I saw hundreds of skeletal figures, specters of human beings, moving forlornly at a glacial pace across the barren Sudanese landscape. Hyenas, accustomed to eating human flesh, routinely picked off small children. I stood over clusters of bleached human bones on the outskirts of villages where dozens of people, too weak to walk, had laid down in a group and never gotten up. Many were the remains of entire families.

In the abandoned town of Mayen Abun bats dangled from the rafters of the gutted Italian mission church. The streets were overgrown with tussocks of grass. The dirt airstrip was flanked by hundreds of human bones, skulls and the remnants of iron bracelets, colored beads, baskets and tattered strips of clothing. The palm trees had been cut in half. People had eaten the leaves and the pulp inside. There had been a rumor that food would be delivered by plane. People had walked for days to the airstrip. They waited and waited and waited. No plane arrived. No one buried the dead.

Now, from a distance, I watch this happen in another land in another time. I know the indifference that doomed the Sudanese, mostly Dinkas, and today dooms the Palestinians. The poor, especially when they are of color, do not count. They can be killed like flies. The starvation in Gaza is not a natural disaster. It is Israel’s masterplan.

There will be scholars and historians who will write of this genocide, falsely believing that we can learn from the past, that we are different, that history can prevent us from being, once again, barbarians. They will hold academic conferences. They will say “Never again!” They will praise themselves for being more humane and civilized. But when it comes time to speak out with each new genocide, fearful of losing their status or academic positions, they will scurry like rats into their holes. Human history is one long atrocity for the world’s poor and vulnerable. Gaza is another chapter.

*

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Featured image: Let Them Eat Dirt – by Mr. Fish

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Niall McCrae: The Shocking Testimony of the COVID-19 Nurses
"Overton observed that covid was killing only people in hospital, not at home nor among the homeless. The treatment regime was devised to end lives efficiently."

Lioness of Judah Ministry
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By Niall McCrae January 25, 2024

Most people seem to have moved on from Covid-19. They may occasionally refer to the ‘pandemic’, but they’d rather put it in the back of their minds. So it’s important that we critical thinkers don’t let the truth be buried by an official narrative that a deadly disease struck, radical interventions were necessary and then a miraculous vaccine saved millions of lives.

I know a nurse who worked throughout covid at the local intensive care unit. She believes that while the disease was exaggerated, it was distinct from the usual respiratory infections. Positively-tested patients admitted to her unit frequently suffered from asthmatic attacks. But such symptoms probably resulted from the terror induced in society by the government. And these patients were right to be terrified, because they faced being hooked on to a ventilator, totally dependent on overworked clinical staff, with no visitors allowed. As Roger Watson and I explained on TCW, many never took another natural breath.

The book What the Nurses Saw by Ken McCarthy features interviews with nurses who worked in the killing fields of US hospitals. An army veteran, Erin Marie Olszewski qualified and practised as a nurse in Florida. When New York became the American epicentre of Covid-19, she answered the urgent call for nurses from the city authorities. On arrival Olszewski was surprised to be boarded in a luxury hotel, having no work assigned but paid $10,000 weekly by the Federal Emergency Management Agency (FEMA). Clearly the crisis was not as bad as portrayed on the news.

Eventually Olszeswki was posted to a large public hospital, to find doctors and nurses following extraordinary and harmful protocols. Rather than a last resort, intubation to breathing machines was primary treatment. Andrew Cuomo, governor of New York, acted as medical dictator, ordering 30,000 ventilators. As paycheck employees following administrative policy, doctors abandoned their Hippocratic Oath, mistreating patients who walked into hospital but left via the morgue. Consent, so fundamental to healthcare, was reduced to doctors telling patients that their only chance of survival was mechanical ventilation.

According to Olszewski the throughput was like a factory production line, manufacturing the desired mortality data. Nurses, normally reticent in challenging decisions made by doctors in a rigid hierarchical culture, failed to put their patients first. They were complicit in state-sanctioned murder. This was particularly awful in the public hospitals of New York, where the majority of patients were poor and funded by Medicare, the federal system that incentivised use of ventilators, paying hospitals $39,000 per case. As patients were expected to perish, little care was given and they lay unwashed on their faeces. As soon as a corpse was carried out, the apparatus was used for the next admission.

Another whistle-blower, Nicole Sirotek, observed that institutional power was rarely needed to ensure nurses’ compliance with the covid regime. The nursing staff policed themselves, making clear that any dissident would be ostracised, imperilling their professional career.

According to Kimberley Overton, a nurse in Nashville, nurses were told not to spend time near patients’ beds to reduce spread of the virus, despite their full exposure in wards dedicated to covid cases. This was unnecessary cruelty. Patients were deliberately isolated, deprived of nutrition and water (drips were regarded as sufficient fluid intake), and communication was impossible with nurses covered head-to-toe in PPE.

Wards should have had a warning at the entrance to abandon hope, all ye who enter here. Overton observed that covid was killing only people in hospital, not at home nor among the homeless. The treatment regime was devised to end lives efficiently. Ventilators were key to this, as Overton described:

‘In all my career, I had never seen the PEEP (positive end-expiratory pressure) settings set so high. Typically we see it at about five, and we were seeing that pressure at fifteen. We were blowing people’s lungs out.’

To sedate intubated patients, high doses of fentanyl were administered. It was standard practice to conduct a breathing test on patients after a day on the ventilator. They almost always failed, because of the respiratory suppressant effect of fentanyl. But the most dubious intervention was remdesivir, declared by Anthony Fauci as the ‘drug of choice’ for covid sufferers. This antiviral was originally tested on Ebola cases, but over half died in the trial. For covid a rushed and incomplete trial was claimed as evidence of its efficacy, but the drug often caused kidney failure.

British readers will be particularly interested in the account of Kevin Corbett. I spoke alongside Corbett at Trafalgar Square in September 2020, when he warned the mass audience of the ‘Nazification’ of the NHS. Covid-19 was not panic by the authorities, but a deliberate and planned takeover of the healthcare system. Individual care, to which taxpaying citizens believe they are entitled, was replaced by Nazi-style viral hygiene. Petty dictators in matrons’ uniform had never enjoyed so much power: no mask, no shift. The rationale for covid rules was never therapeutic, but exertion of totalitarian authority.

The NHS was bad, but American hospitals were much worse. The profit incentive was irresistible to unscrupulous administrators, with incredibly high payments for concluded cases (i.e. deaths). Another factor is that senior managers and clinicians of Democrat leanings were dealing with patients of lower socio-economic status and populist Trump proclivities. Vaccination rates in the US confirmed this political divide.

The motto, should another pandemic be declared (Disease X, as the media are priming), is ‘stay out of hospital’. That’s a terrible indictment on doctors and nurses, so many of whom broke their code of conduct to participate in crimes against humanity.

What the Nurses Saw should be required reading for politicians, administrators and clinicians who uncritically accepted and applied the Covid-19 orthodoxy. McCarthy’s compendium of bedside experiences shows what happens when all professional and moral standards are abandoned in favour of a globally enforced problem-reaction-solution contrivance. As Bill Gates excitedly foresees, there will be a ‘next time’, and if as a society we do not learn the lessons from the pseudopandemic and confront the evil-doers, we deserve whatever follows.

Source: conservativewoman.co.uk

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https://lionessofjudah.substack.com/p/niall-mccrae-the-shocking-testimony


https://donshafi911.blogspot.com/2024/01/niall-mccrae-shocking-testimony-of.html

Screening for Silent Spike Toxicity
Spike levels build up over time with repeated exposures and eventually the dam breaks. Here's how to detect toxicity before it causes symptoms.

Dr. Syed Haider
Pet Toxin Safety - Mill Creek Animal Hospital
This post will provide a deep dive on tests for spike toxicity, including the best screening tests for those who have no symptoms, but have been exposed. These tests detect specific spike-induced inflammation, clotting, AIDS, turbo cancer, etc, and can help get ahead of disease developing underneath the surface. In a future post I plan to cover the best tests for fine tuning a healing protocol.

There are now hundreds if not thousands of physicians treating spike toxicity with varying protocols and degrees of success.

In my experience most hesitate to escalate ivermectin enough. At high enough doses it almost always helps (at mygotodoc.com I usually start where others end, at 0.2mg/kg/day and then may gradually escalate as high as 10 times more than that ie 2mg/kg/day in some patients over the course of 5-10 weeks).

Most physicians treating spike toxicity also refrain from much or any testing.

This makes sense on a budget, and I often come across patients who can’t afford testing and we skip it as well, but if it can be afforded then it can be helpful in fine tuning the protocol and sometimes uncovering key missing ingredients, like nutritional deficiencies, or particularly stubborn micro clotting requiring escalated dosing and varied types of anticoagulants.

The other place for testing is in screening of the general population without symptoms, both vaxxed and unvaxxed (though when you really press you often do find new symptoms have sprouted up since the beginning of the pandemic).

But even in those who truly have no new symptoms and feel perfectly fine, it seems that it may simply be a matter of time before spike toxicity catches up with them, especially if, like so many people, they can’t detox quickly enough, can’t break up the atypical microclots fast enough, and then are reexposed to a new variant, or a big shedding bolus, and that tips the scales and sends them into outright long haul.

People find it hard to believe that they could feel fantastic and yet there could be something brewing inside that is just 1 straw away from breaking their backs.

Yet almost everyone was in this very situation even before the pandemic.

We all have a health span and a lifespan, and for most in the modern world the overlap between them has been dramatically shrinking for generations, and it has only gained speed with each passing year, and especially the last 3 years since the pandemic hit.

Health is wealthqbak - http://asianpin.com/health-is-wealthqbak/ | Funny cartoons jokes, Funny cartoon pictures, Funny cartoons
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In plain English, we often gradually become chronically ill and then debilitated starting decades before we finally die. In the worst cases spending the last years of our lives in nursing homes, oblivious to our surroundings and infrequently visiting loved ones.

The reason for this is a chronic mismatch between our bodies and our environments - not just lack of exercise and poor diets, but also the chemical soup we find ourselves in, the toxins in the air, water and soil, the lack of fresh air and sunlight throughout the day, the lack of grounding, and too much toxic blue light at night that is soaked up by our eyes and very skin while we lounge in front of our screens, greatly stressing ourselves, while thinking we’re relaxing, followed by restless, unfulfilling sleep.

Most of us are drawing down on our health savings accounts - not the tax free HSA - but a metaphorical account that represents our life force.

Thank you for reading Dr. Syed Haider. This post is public so feel free to share it.

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Just like a regular bank account, if it isn’t managed properly and wealth is overused, it will eventually get close to zero, by which time we will be liable to illness at the drop of a hat - anything that is too taxing can overdraw the account since what’s flowing into it can’t overcome what’s flowing out.

And then some of us become chronically overdrawn, living on credit, and in the toxic embrace of chronic illness because of it, dragging us into the depths, while we struggle vainly to get back above the surface.

This is why when you finally realize you have to change your ways to get better, it makes no sense to give up those changes as soon as you break free of illness.

You are just above zero, still liable to dipping below the surface again. You need to build up your reserves of health over time and not overdraw your account again. You have to become a good steward of your body and resources. And over time you can get to the point where you’re on solid ground again and can put up with small and large stressors without backsliding. But you should always keep in mind how bad it can get to motivate you to stay on the straight and narrow going forward.





To get back to the topic, the spike protein builds up in our bodies over time and causes detectable changes to our immune and vascular systems. There is an immune fingerprint of various cytokine markers, there are the microclots, there are alterations to the red blood cell zeta potential, there are predictable decreases of various micronutrients. There may be early warning signs of AIDS, or cancer or organ dysfunction.

Nowadays almost all new patients with Long COVID or Vax injury made it through a few shots, or a few rounds of COVID without getting long haul, but the final infection or shot put them over the edge.

If they had come before they got that last shot or infection I could have detected their susceptibility in the lab and we could have worked to correct it.

This is the epidemic of Silent Spike Toxicity.

And these are the tests we have available to screen for it:

The Microclot Test: only available from 1 lab in the US (mail order). Detects abnormal clotting not seen on any other test. The single most specific spike toxicity test.

The Comprehensive Spike Screening Panel: includes imaging tests: EKG, CXR, Echo. Blood tests that detect damage to the heart, lungs, liver, kidneys. Checks zeta potential. Can show the immune fingerprint of spike. Detection of AIDS. Typical gut microbiome changes. Advanced cancer screening (blood & whole body MRI), and more.

The Masterjohn-Schilling Spike Healing Panel: detects neuroinflammation, free radicals, mitochondrial dysfunction, autoantibodies, reactivated viruses and bacteria, MCAS, specific micronutrients that are depleted by spike toxicity, and more.

Masterjohn’s Deep Dive Nutrition Panel goes beyond nutrients depleted by spike toxicity to provide a complete snapshot of functional nutrition and is indispensable for deep healing when half measures don’t work.


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A quick note on tests in general: There is no perfect test. Tests are evaluated by their sensitivity and specificities, but we don’t have research on any of these for spike toxicity diseases. Sensitivity is how good a test is at ruling out a diagnosis and specificity is how good it is at ruling in a diagnosis.

The best screening tests would be 100% specific - meaning if you have the diagnosis it will be detected 100% of the time, but in order to gain that level of specificity they often have to cast a wide net and give up some sensitivity. What this means practically is that if the diagnosis is present you will test positive, but there will also be some people who don’t have the diagnosis who also test positive.

Highly specific tests are usually paired with confirmatory tests that are hopefully highly sensitive. Meaning they can weed out the people who were including in the first round of screening, but don’t actually have the diagnosis in question.

In the absence of research into spike toxicity diseases and optimal screening regimens we have to fall back on expert opinion.

It seems that the microclot test is likely the best screening test, because those treating spike toxicity have never come across someone with the clinical symptoms of the disease who doesn’t have elevated microclots. Unfortunately microclots can be elevated by other conditions. So a confirmatory test like the incelldx Incellkyne panel might be ordered from the Comprehensive Spike Screening panel, along with other tests we’ll discuss below.

If the diagnosis of spike toxicity is made then the Masterjohn-Schilling panel is the best next step for fine tuning the protocol, ensuring that the right micronutrients are topped up and the right treatments are prescribed.

If not improving after targeted and sustained treatment, then the Deep Dive Nutrition panel is indicated to uncover rare and unusual nutritional deficits that could be holding you back.

Here I’ll cover the primary screening tests: The Microclot Test and the Comprehensive Spike Screening Panel. In a future article I may cover the more expansive and complicated panels that are used primarily in treatment.

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The Microclot Test

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Typical microclots are usually found in the elderly and those with chronic illnesses like diabetes.

Spike induced atypical amyloid fibrin microclots are found in those with spike induced blood toxicity.

The difference between typical and atypical are that spike induced microclots are very difficult to break down, so difficult that they often do not break down at all.

This explains why the D-dimer isn’t helpful for detecting spike toxicity.

D-dimer is always trapped inside of clots. Typical clots are always being broken down on the margins - at the edge of a typical clot there will be breakdown. Sometimes the breakdown happens slower than the growth of the clot, but there is always a battle going on between clot growth and clot destruction which will release D-dimer into the blood stream.

Since it is virtually always elevated in the presence of clotting it is a very specific test, and is used as a screening test when a physician suspects a clotting disorder, but isn’t sure. For example if someone shows up with chest pain and it could be a pulled muscle or a pulmonary embolism (clot in the pulmonary veins), a D-dimer is a simple ad very cheap test that can be done to determine if further confirmatory, but more expensive more risky testing should be considered, like a CT Angiogram of the chest.

For this reason every doctor going through residency comes to consider a positive D-dimer as indicative of clotting and a negative D-dimer as indicative of no clotting.

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The D-dimer is often elevated during severe acute COVID-19 infection, and during a severe acute injection reaction, but it is not usually elevated in chronic spike toxicity, including chronic long haul and vaccine injured patients.

The reason it isn’t elevated is that most people cannot break down the atypical microclots caused by spike protein without some additional help from medications and supplements.

Once medications like aspirin (and sometimes prescriptions ones like plavix and eliquis), supplements like nattokinase, serrapeptase, lumbrokinase, bromelain and NAC are started the atypical microclots start to be broken down and D-dimer goes up, which in this case is usually reason for celebration.

So the microclot test is the only test in America today that can detect elevated atypical microclots. It’s only available from one lab in the country via mail order (request it from mygotodoc.com), and it helps detect spike toxicity as well as helping track treatment.


If initial treatment for microclots with aspirin and supplements doesn’t bring the levels down then we escalate to using higher doses, or add plavix and then later eliquis. And we can also consider plasma donation, or even therapeutic plasmapheresis, if available.



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The Comprehensive Spike Screening Panel

This set of tests includes an EKG, CXR, Echo. It includes blood tests to screen for daamage to the major organs including the heart, lungs, liver, and kidneys. It checks for zeta potential in the blood, which is affected by spike toxicity. It detects an immune fingerprint of spike. It can detect AIDS. It covers stool testing for the gut microbiome as well as advanced cancer screening (via blood & whole body MRI), and more.

Tests Included in the Panel:

Spike antibody test: Measures your B cell’s response to the spike protein. In the absence of a direct test for spike protein this helps indirectly detect and track the spike protein levels in your body. Your body produces antibodies in response to the spike protein, and this test measures those antibodies. Generally speaking the more spike protein in your body, the higher the antibody levels. However, what's considered a problematic level varies by individual. The goal is to lower this level as much as possible. The test can also help detect those individuals who might be transmitting the spike protein to others. This is by no means a perfect test, but in the right setting it is helpful as a red flag for further workup, or as a way of monitoring response to therapies over time.

Incellkyne Panel from Incelldx - provides an immune fingerprint of spike protein, a combination of elevated cytokine markers that are typically seen in spike protein disease. There are other immune fingerprints they have identified on this same test that indicate non spike Chronic Fatigue Syndrome and Lyme disease. If CCL-5/RANTES and/or VEGF are elevated (VEGF is almost always elevated) then the medication Maraviroc can be helpful. VEGF indicates vascular inflammation and omega-3s, infrared light exposure, and a number of other approaches can be particularly helpful to deal with that. Other inflammatory markers tested are TNF-alpha, IL-2, IL-4, IL-6, IL-8, IL-10, IL-13, GM-CSF, SCD40L, CCL3, CCL-4, and IFN-Gamma. Ivermectin is known to decrease IL-6, which is commonly elevated in Long Haul and Vax injury.

Lymphocyte Subset Panel or Cyrex Lymphocyte MAP:



The subset panel is the standard test for AIDS and tests for these immune subsets: CD3, CD19,CD20, CD4, CD8, CD56+. The primary pathognomic feature of AIDS would be a CD4 T cell count lower than 200, though there are other red flags such as NK cell activity <10%, or a deficit of T helper cells (CD4+), as well as these others that would only be found on the Cyrex Lymphocyte MAP test: TH1 insufficiency, Increased T-Reg (CD4+ CD25+), deficits of cytotoxic cells (CD8+, CD56+), increased TGF-beta, etc. The Lymphocyte subset panel is cheaper and available at any standard lab and may be covered by insurance, the Cyrex test is more expensive and is a mail order blood test only that has to be paid in cash up front. The Cyrex test can detect 14 different immunotypes and reveal immune under or overactivity, infections, inflammation, autoimmunity, allergies, asthma, hypersentivities and some cancers. It also helps determine what further immune tests can be done to fine tune a healing protocol.

Galleri Cancer Screening is an advanced test for 50+ types of common cancers based on a genetic marker found in the blood. It is a good screening test because it is 99.5% specific. This might be a good option for someone with a family or personal history of cancer as it can detect occurance at a the earliest microscopic stage, far before any visual test like an MRI or CT scan would show a mass. If cancer is found ivermectin, fenbendazole, vitamin C, baking soda and many other of label easily available substances are very promising for treatment.

Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer?

Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer?
Cancer rates have skyrocketed in the past century for a number of reasons not least of which is the incredibly large number of toxins spewed into the environment and incorporated into our food supplies. And now with most of humanity exposed to the cancerous spike protein there is likely to be even further acceleration. Those exposed to the fallout from …

Read full story

Complete Blood Count (CBC)


Measures various components and features of the blood, including red blood cells, white blood cells, and platelets. Amongst the white blood cells we can see various abnormalities - they can be high or low, and subsets like basophils, neutrophils and eosinophils might be off. For example a patient started aspirin which is a cornerstone of most treatments of spike toxicity, but in this case raised the eosinophil level and caused some histaminergic symptoms. The symptoms were the same as her usual disease symptoms so initially were written off as a normal fluctuation in symptomatology over time, but in light of the elevated eosinophil level we finally determined that the aspirin was triggering a problem, since that is possible side effect of aspirin. Once off aspirin the symptoms and the eosinophils normalized.

Comprehensive Metabolic Panel (CMP)


Measures 14 different substances in the blood. It provides information about kidney and liver function, electrolyte levels, and blood sugar. Blood sugar can be high or low in spike toxicity, and that would indicate a pancreatic issue requiring further workup. Liver function often needs to be tracked in those on ivermectin and many other medications. Potassium balances sodium and usually needs to be supplemented in long haul, since most people don’t get enough, especially if blood pressure is rising.

Cystatin C is a more specific marker of kidney dysfunction than the creatinine level that is included on the CMP.

D-dimer: as mentioned earlier this is a product of the breakdown of clots, it’s often elevated in the acute phase of spike injury or disease, but over time the microclots being inherently difficult to break down stop releasing D-dimer unless the patient is taking a combination of supplements and/or medications to trigger this.

Erythrocyte Sedimentation Rate (ESR)

Decoding ESR Test: What Your Results Could Reveal About Your Health | Pathkind Labs Blog
Measures the rate at which red blood cells settle in a standardized tube over one hour. It is a nonspecific marker of inflammation in the body. It is also an indication of the zeta potential, which is a measure of the normal negative charge on red cells that prevents them from clumping together. Spike protein lowers the normal zeta potential which usually causes ESR to rise. Potassium citrate can help reverse this trend, as can sunlight and grounding.

hs-CRP Test (C-Reactive Protein High-Sensitivity) is another non specific marker of inflammation in the body and if found require further workup. It can be elevated in myo-pericarditis.

Troponin T is a protein relatively specific to heart muscle cells, leaked into the blood. This is a cardiac biomarker that indicates myocardial injury and along with an EKG is. one of the primary screening tests for a heart attack as well as for myocarditis/pericarditis.

Pro BNP (N-terminal pro-brain natriuretic peptide) is produced by the heart in response to strain, particularly heart failure.

Electrocardiogram (EKG)

EKG: What is it and what does it mean? – JP Stroke Foundation
Non-invasive medical test that records the heart's electrical activity. Can be used to diagnose myocarditis/pericarditis, heart attack, and various rhythm abnormalities like atrial fibrillation, SVTs and more that can raise the risk of sudden cardiac arrest, such as that seen in some athletes who have been vaxxed.

Echocardiogram (ECHO)


Provides valuable information about the heart's structure, function, and blood flow and is an important test for helping visualize the inflammatory changes of myocarditis-pericarditis, such as fluid leaking into the sack around the heart.

Chest X-ray


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Non-invasive imaging test that uses X-rays to visualize the structures and organs within the chest, including the lungs, heart, ribs, diaphragm, and large arteries. Anyone with shortness of breath should have a Chest Xray as a first screening test looking for pneumonia, inflammation, scarring, nodules/cancer, etc.

Whole Body MRI

The Latest Quantified Self Trend: Whole-Body MRI
Another imaging modality that can turn up hidden cancers and a whole host of other abnormalities and might be ordered for someone where the Galleri test was negative but there was still some suspicion present (here is always the risk of over diagnosis with imaging tests like this, which can lead to otherwise unnecessary stress and procedures that can themselves cause harm).

Microbiome testing: Microbiomix Metagenomic Sequencing of Stool by Genova or Sabine Hazan’s Whole Genome Deep Sequencing by Progenabiome. Spike toxicity leads to depletion of beneficial gut bacterials species such as Bifidobacterium pseudocatenulatum, Faecalibacterium prausnitzii, Roseburia inulinivorans, and Roseburia hominis all of which are associated with long COVID complications. Presence of 'unfriendly' bacterial species is linked to poor performance on the 6-minute walk test among long COVID patients. Microbiomix is cheaper because it uses a less thorough sequencing technique, but can show some changes found due to spike toxicity. Sabine Hazan’s test is better if budgeting allows, both because it does a whole genome sequencing, but also because it benefits from her proprietary and private knowledge base (essentially studies and findings that have not yet been published). There are some supplements that can help correct deficits, and in stubborn cases a stool transplant can be transformative, though this is somewhat difficult to get done as it usually requires travel.





And that’s a wrap!

Next time We’ll look at the Masterjohn-Schilling panel which is our go to for optimizing treatment of long haul/vax injury and perhaps the Comprehensive Nutrition panel, which is important for anyone who has a chronic illness resistant to treatment, including long haul syndromes.

https://blog.mygotodoc.com/p/screening-for-silent-spike-toxicity

https://telegra.ph/Screening-for-Silent-Spike-Toxicity-01-07

Everything to know about the Health Benefits of Beets
Some benefits of eating beets may include lower blood pressure and better athletic performance, among others. Eating beets raw or juicing and roasting them may be more beneficial than boiling them.

Beetroots, commonly known as beets, are a vibrant and versatile type of vegetable. They’re known for their earthy flavor and aroma. Many people call them a superfood because of their rich nutritional profile.

In addition to bringing a pop of color to your plate, beets are highly nutritious and packed with essential vitamins, minerals, and plant compounds, many of which have medicinal properties.

What’s more, they’re delicious and easy to add to your diet in dishes like balsamic roasted beets, hummus, fries, and salads, among many others.

Here are 9 evidence-based benefits of beets, plus some tasty ways to increase your intake.

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Beets boast an impressive nutritional profile.

They’re low in calories yet high in valuable vitamins and minerals. In fact, they contain a bit of almost all of the vitamins and minerals your body needs (1Trusted Source).

Here’s an overview of the nutrients found in a 3.5-ounce (100-gram) serving of boiled beetroot (1Trusted Source):

Calories: 44
Protein: 1.7 grams
Fat: 0.2 grams
Carbs: 10 grams
Fiber: 2 grams
Folate: 20% of the Daily Value (DV)
Manganese: 14% of the DV
Copper: 8% of the DV
Potassium: 7% of the DV
Magnesium: 6% of the DV
Vitamin C: 4% of the DV
Vitamin B6: 4% of the DV
Iron: 4% of the DV
Beets are particularly rich in folate, a vitamin that plays a key role in growth, development, and heart health (2Trusted Source).

They also contain a good amount of manganese, which is involved in bone formation, nutrient metabolism, brain function, and more (3Trusted Source).

Plus, they’re high in copper, an important mineral required for energy production and the synthesis of certain neurotransmitters (4Trusted Source).

Summary
Beets are loaded with vitamins and minerals yet low in calories and fat. They’re also a good source of several key nutrients, including folate, manganese, and copper.

Beets have been well studied for their ability to decrease elevated blood pressure levels, which are a major risk factor for heart disease (5Trusted Source).

In fact, some studies show that beetroot juice could significantly lower levels of both systolic and diastolic blood pressure (6Trusted Source, 7Trusted Source).

The effect appears to be greater for systolic blood pressure, which is the pressure when your heart contracts, rather than diastolic blood pressure, which is the pressure when your heart is relaxed. Also, raw beets may exert a stronger effect than cooked ones (7Trusted Source, 8Trusted Source).

These blood-pressure-lowering effects are likely due to the high concentration of nitrates in this root vegetable. In your body, dietary nitrates are converted into nitric oxide, a molecule that dilates blood vessels and causes blood pressure levels to drop (9Trusted Source).

Beets are also a great source of folate. Although research has turned up mixed results, several studies suggest that increasing your intake of folate could significantly lower blood pressure levels (10Trusted Source).

However, keep in mind that beets’ effect on blood pressure is only temporary. As such, you need to consume them regularly to experience heart-health benefits over the long term (11Trusted Source).

Summary
Beets contain a high concentration of nitrates, which can help lower your blood pressure levels. This may lead to a reduced risk of heart disease and stroke.

Several studies suggest that dietary nitrates like those found in beets may enhance athletic performance.

Nitrates appear to affect physical performance by improving the efficiency of mitochondria, which are responsible for producing energy in your cells (12Trusted Source).

According to one review, beetroot juice could enhance endurance by increasing how long it takes to become exhausted, boosting cardiorespiratory performance, and improving efficiency for athletes (13Trusted Source).

Promisingly, beet juice has also been shown to improve cycling performance and increase oxygen use by up to 20% (14Trusted Source, 15Trusted Source).

It’s important to note that blood nitrate levels peak within 2–3 hours of consuming beets or their juice. Therefore, it’s best to consume them a couple of hours before training or competing to maximize their potential benefits (16Trusted Source).

Summary
Eating beets may enhance athletic performance by improving oxygen use and endurance. To maximize their effects, consume them 2–3 hours prior to training or competing.

Beets contain pigments called betalains, which possess a number of anti-inflammatory properties (8Trusted Source, 17Trusted Source, 18Trusted Source).

This could benefit several aspects of health, as chronic inflammation has been associated with conditions like obesity, heart disease, liver disease, and cancer (19Trusted Source).

One study in 24 people with high blood pressure found that consuming 8.5 ounces (250 mL) of beet juice for 2 weeks significantly reduced several markers of inflammation, including C-reactive protein (CRP) and tumor necrosis factor-alpha (TNF-a) (8Trusted Source).

Plus, an older 2014 study in people with osteoarthritis — a condition that causes inflammation in the joints — showed that betalain capsules made with beetroot extract reduced pain and discomfort (20).

Beetroot juice and extract have also been shown to reduce kidney inflammation in rats injected with toxic, injury-causing chemicals (17Trusted Source).

Still, more studies in humans are needed to determine whether enjoying beets in normal amounts as part of a healthy diet may provide the same anti-inflammatory benefits.

Summary
Beets may have a number of anti-inflammatory effects, although further research in humans is needed.

One cup of beetroot contains 3.4 grams of fiber, making beets a good fiber source (1Trusted Source).

Fiber bypasses digestion and travels to the colon, where it feeds friendly gut bacteria and adds bulk to stools (21Trusted Source).

This can promote digestive health, keep you regular, and prevent digestive conditions like constipation, inflammatory bowel disease (IBS), and diverticulitis (22Trusted Source, 23Trusted Source).

Moreover, fiber has been linked to a reduced risk of chronic diseases, including colon cancer, heart disease, and type 2 diabetes (23Trusted Source, 24Trusted Source, 25Trusted Source).

Summary
Beets are a good source of fiber, which benefits your digestive health and reduces the risk of several chronic health conditions.

»MORE:Living with diabetes? Explore our top resources.
Mental and cognitive functions naturally decline with age, which can increase the risk of neurodegenerative disorders like dementia.

The nitrates in beets may improve brain function by promoting the dilation of blood vessels and thus increasing blood flow to the brain (26Trusted Source).

Particularly, beets have been shown to improve blood flow to the frontal lobe of the brain, an area associated with higher level thinking like decision making and working memory (27Trusted Source).

Furthermore, an older study in people with type 2 diabetes found that reaction time during a cognitive function test was 4% faster in those who consumed 8.5 ounces (250 mL) of beetroot juice daily for 2 weeks, compared with a control group (28Trusted Source).

However, more research is needed to determine whether beets could be used to improve brain function and reduce the risk of dementia among the general population.

Summary
Beets contain nitrates, which may increase blood flow to the brain and improve cognitive function. However, more research in this area is needed.

Beetroot contains several compounds with cancer-fighting properties, including betaine, ferulic acid, rutin, kaempferol, and caffeic acid (29Trusted Source).

Although more research is needed, test-tube studies have shown that beetroot extract can slow the division and growth of cancer cells (30Trusted SourceTrusted Source, 31Trusted Source, 32Trusted Source).

Several other studies have found that having higher blood levels of betaine may be associated with a lower risk of developing cancer (33Trusted Source, 34Trusted Source).

However, it’s important to note that most studies on the topic have used isolated compounds rather than beetroot. Therefore, further research on beetroot consumption as part of a well-rounded diet and cancer risk is needed.

Summary
Some studies show that certain compounds found in beets could have cancer-fighting properties. Still, further research is needed to better understand this potential connection.

Beets have several nutritional properties that could make them a great addition to a balanced diet.

First, they’re low in fat and calories but high in water, which can help balance your energy intake. Increasing your intake of low calorie foods like this root vegetable has also been associated with weight loss (35Trusted Source).

Furthermore, despite their low calorie content, they contain moderate amounts of protein and fiber. Both of these nutrients can make it easier to achieve and maintain a moderate weight (36Trusted Source, 37Trusted Source).

The fiber in beets may also support digestive health, decrease appetite, and promote feelings of fullness, thereby reducing your overall calorie intake (38Trusted Source).

Additionally, by including them in smoothies or other recipes, you can easily increase your intake of fruits and vegetables to improve the quality of your diet (39Trusted Source).

Summary
Beets have are high in water, moderate in fiber and protein, and low in calories. All of these properties can balance your energy intake and improve your diet quality.

Beets are not only nutritious but also incredibly delicious and easy to incorporate into your diet.

You can juice, roast, steam, or pickle them. For a convenient option, you can purchase them precooked and canned. You can even enjoy them raw, either sliced thinly or grated.

Choose beets that feel heavy for their size with fresh, unwilted green leafy tops still attached, if possible.

Because dietary nitrates are water-soluble, it’s best to avoid boiling beets if you’d like to maximize their nitrate content.

Are beets good for people with diabetes?

Here are some delicious and interesting ways to add more beets to your diet:

Salad. Grated beets make a flavorful and colorful addition to coleslaw or other salads. Try this recipe for Amazing Dressed Beets or a Beetroot, Orange, and Carrot Salad.
Dip. Beets blended with Greek yogurt and fresh garlic make a delicious, healthy, and colorful dip. Have a go at this Beetroot and Honey Lemon Houmous.
Juice. Fresh beetroot juice is typically better than store-bought versions, which can be high in added sugar and contain only a small amount of beets. Try this beetroot juice recipe, which uses carrot, apple, ginger, celery, and lemon for flavor
Soup: Borscht is a popular soup in Eastern Europe and Northeast Asia. Try this classic recipe or this beetroot and tomato variation.
Leaves. You can cook and enjoy fresh beet leaves similarly to how you’d use spinach. Get some ideas for cooking beet greens here.
Roasted. Wedge beetroots and toss them with a little olive oil, salt, pepper, and herbs or spices of your choice. Then, roast them in a 400°F (205°C) oven for 15–20 minutes until they’re tender. Or try these Balsamic Roasted Beets.
Summary
Beetroot is a delicious and versatile vegetable that’s easy to add to your diet. If possible, choose beets that feel heavy for their size with green tops still attached.

Can you eat beets everyday?

It’s always best to follow a varied diet.

Eating a small amount of beetroot every day is unlikely to do any harm, but a high intake could lead to low blood pressure, red or black urine and feces, and digestive problems for anyone with a sensitivity to the nutrients. A high daily beet consumption may also mean you are not getting nutrients from other foods, however, so try to vary your diet.

Always speak with a doctor before making significant dietary changes.

Are beets a superfood?

Some people call beets a superfood because they are rich in essential nutrients.

Are beets anti-inflammatory?

Beets contain betalains, a natural coloring agent with antioxidant and anti-inflammatory properties. Some research suggests belatains may help reduce both symptoms and biological markers in the body related to inflammation (8Trusted Source, 17Trusted Source, 20).

Can beets boost your sexual health?

Beets contain nitrates and there is some evidence they may improve the body’s nitric oxide production (40Trusted Source).

The body needs nitric oxide to open the blood vessels that are necessary for getting and maintaining an erection. This may make them suitable for people with erectile dysfunction, although there is no scientific evidence to confirm this.

Can beets help with sexual function?

Beets are highly nutritious and loaded with health-promoting properties.

They can support the health of your brain, heart, and digestive system, are a great addition to a balanced diet, boost athletic performance, help alleviate inflammation, and possibly slow the growth of cancer cells.

Best of all, beets are delicious and easy to include in your diet. For example, they’re a great addition to salads, side dishes, smoothies, dips, and juices.

https://www.healthline.com/nutrition/benefits-of-beets#nutrients-and-calories

EXCLUSIVEInside NIH virus lab in Montana - that has eerie ties to Wuhan - where US scientists inject pigs and monkeys with EBOLA and other dangerous bio-agents
By Alexa Lardieri U.S. Deputy Health Editor Dailymail.Com 14:57 GMT 27 Jan 2024 , updated 14:57 GMT 27 Jan 2024

Photos obtained by a watchdog group show experiments performed on animals
NIH lab in Montana was previously found to have been experimenting with SARS
REVEALED: NIH lab experimented with coronaviruses from Wuhan in 2018
Photos and videos obtained exclusively by DailyMail.com show US government-funded researchers experimenting on animals at a controversial lab in Montana where risky virus research is carried out.

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Images and video footage obtained through a Freedom of Information Act request and shared exclusively with this website show researchers sedating monkeys and pigs and giving them injections, as well as piglets housed in small and unsanitary cages.

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While there is no suggestion any of the footage shows illegal activity, it gives an eerie glimpse into what goes on at the National Institutes of Health's Rocky Mountain Lab (RML), which has come under scrutiny in recent months.

Last year, this website revealed that RML in Montana had been experimenting with SARS-like viruses a year before the Covid pandemic, and while that research has stopped, current projects involving other deadly pathogens with the potential to spark a new pandemic are still being carried out at the lab.

These include injecting pigs with Ebola and infecting monkeys with Covid-19 and studying how they react to Hemorrhagic Fever, which involves vomiting blood, internal bleeding, bleeding in the brain and from the eyes, nose and mouth.

The documents reveal NIH scientists proposed infecting two- to three-week old piglets with reston virus (REBOV), a family of pathogens that could cause Ebola, for a project to take place between 2017 and 2020
The documents reveal NIH scientists proposed infecting two- to three-week old piglets with reston virus (REBOV), a family of pathogens that could cause Ebola, for a project to take place between 2017 and 2020
The White Coat Waste project obtained photos of animal experiments on monkeys and pigs at the National Institutes of Health's Rocky Mountain Lab in Montana
The White Coat Waste project obtained photos of animal experiments on monkeys and pigs at the National Institutes of Health's Rocky Mountain Lab in Montana
The National Institutes of Health's Rocky Mountain Lab in Montana was previously found to have been experimenting with SARS-like viruses in 2018
The National Institutes of Health's Rocky Mountain Lab in Montana was previously found to have been experimenting with SARS-like viruses in 2018
Piglet experiments were to be carried in two parts, first infecting the pigs with REBOV via their noses - as seen in the photos above
Piglet experiments were to be carried in two parts, first infecting the pigs with REBOV via their noses - as seen in the photos above
The footage was obtained through a FOIA request by the White Coat Waste Project (WCW), which has campaigned against risky virus research and cruel animal experiments.

The RML was first revealed to be experimenting with deadly pathogens in WCW's first batch of documents provided to this website last year.

Previous documents from WCW revealed that in 2018, NIH researchers infected bats at the Rocky Mountain Lab with a 'SARS-like' virus as part of a collaboration with the Wuhan Institute of Virology, which is at the center of the Covid cover-up scandal.

They showed US taxpayer money was used to experiment with coronaviruses from the Chinese lab thought to be the source of the Covid pandemic more than a year before the global outbreak.

The NIH, under Dr Anthony Fauci's leadership, infected 12 Egyptian fruit bats with a 'SARS-like' virus called WIV1 at RML.

The WIV1-coronavirus was shipped from the Wuhan lab the FBI believes caused the Covid pandemic and was tested on bats acquired from a 'roadside' Maryland zoo.

Senators probe Fauci-run virus lab in Montana where US scientists were infecting bats with Covid-like viruses shipped in from WUHAN in 2018 - years before the pandemic


Senators are demanding answers about a laboratory in Montana where US taxpayer money was used to manipulate coronaviruses before the pandemic.

The research determined the novel virus could not cause a 'robust infection,' but is more evidence of ties between the US government and the Wuhan lab, as well as the funding of dangerous virus research across the globe.

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Following the WCW's investigation and DailyMail.com's reporting, Republican Senators Joni Ernst, from Iowa, and Eric Schmitt, from Missouri, sent a letter to the NIH demanding 'to learn more about potentially risky research' carried out by scientists at RML.

Most recently, Sen Ernst wrote another letter, along with Rep Mike Gallagher, to the Pentagon demanding a review of the $50million in grants the US is sending to Chinese pandemic research institutions, including those based in Wuhan.

The senator said in a statement: 'Taxpayers deserve to know how much of their money is being shipped to China and why Washington continues collecting and creating deadly super viruses — both of which could pose threats to our national security.'

While the 'SARS-like' virus research has stopped, current projects involving other deadly pathogens with the potential to spark a new pandemic are still being carried out at the lab.

As part of WCW's current lawsuit, the NIH was compelled to send the group records of its experiments taking place at RML.

The documents reveal NIH scientists proposed infecting two- to three-week old piglets with reston virus (REBOV), a family of pathogens that could cause Ebola, a virus with a death rate of up to 90 percent, for a project to take place between 2017 and 2020.

The project, 'The role of Arterivirus co-infection in the pathogenesis of Reston Ebola Virus in swine', was to test how the co-infection of Porcine Reproductive and Respiratory Syndrome (PRRS) and REBOV increased the virus' transmissibility and severity.

The experiment was to be carried out in two parts, first infecting the pigs with REBOV via their noses - as seen in photos.

On day three and between days five and 10 after inoculation, four animals were to be euthanized so necropsies could be performed.

The remaining animals were to be euthanized on day 28. Then, researchers proposed inoculating pigs with PRRSV and REBOV several days later to observe their behavior and take vitals then euthanize them on day 28.

One study was to evaluate up to three species of nonhuman primates as potential animal models for Covid-19. For each species, one group of eight animals would be inoculated with a high dose of the virus via the eyes, nose or mouth
One study was to evaluate up to three species of nonhuman primates as potential animal models for Covid-19. For each species, one group of eight animals would be inoculated with a high dose of the virus via the eyes, nose or mouth
In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19
In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19
In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19
In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19
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While experimental 'manipulations' were to take place while the pigs were under anesthesia, the researchers said, 'Since we are evaluating these animals as potential models of disease progression, we are unable to alleviate the signs of disease.'

Symptoms of these diseases include fever, breathing problems, weight loss, diarrhea, excessive or internal bleeding, coughing up or vomiting blood and neurological disorders that could be fatal.

Researchers said: 'The illness experienced by animals exposed to these viruses must not be treated with analgesics because treatment will interfere with studying the disease manifestation and ultimate outcomes of infection.'

In additional documents obtained by WCW, scientists proposed experiments between 2019 and 2022 on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever, a tick-borne virus that causes a life-threatening fever, muscle and joint pain, liver and kidney failure or pulmonary failure.

The proposal said: 'In previous studies animals were scored for... reduced movement in cage and edema that on rare instances was of severity sufficient to impair function of internal organs such as the lungs and intestines.

'Since the objective of this study is to evaluate the efficacy of DNA vaccine candidates against CCHFV and contains necessary irrelevant DNA control group it is expected that some or animals will develop clinical signs and may suffer pain and distress.

'The illness experienced by the animals exposed to CCHFV must not be treated with analgesics because treatment could interfere with the disease manifestation and the outcome of vaccination.'

Photos show piglets housed in small and unsanitary cages
Photos show piglets housed in small and unsanitary cages
Photos show piglets housed in small and unsanitary cages
Photos show piglets housed in small and unsanitary cages
A third proposal for experiments between 2020 and 2023 was titled 'Nonhuman primate model development for the novel coronavirus emerging in Wuhan, China.'

The aim was to evaluate up to three species of nonhuman primates as potential animal models for Covid-19. For each species, one group of eight animals would be inoculated with a high dose of the virus via the eyes, nose or mouth - as seen in photos.

The primates were to be evaluated and have their vitals taken and on day three, four would be euthanized. The remaining were to be monitored for disease progression.

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The proposal read: 'Infection with 2019-nCoV may cause mild to severe disease in nonhuman primates. Signs of illness may include fever, malaise, fatigue cough and heavy breathing potentially resulting in acute respiratory distress; the infection may be fatal.

'However, in this study we are unable to alleviate the disease manifestations potentially associated with 2019-nCoV infection as treatment would interfere with the outcome of the study.'

Justin Goodman, the senior vice president of the White Coat Waste Project told DailyMail.com: 'Our successful lawsuit has pierced the veil of secrecy around the NIH’s dangerous, wasteful, and cruel maximum pain animal experiments with deadly bioagents that have up to 100 percent kill rates in humans.

'We’ve uncovered how NIH gain-of-function researchers linked to EcoHealth and the Wuhan lab import primates to the Rocky Mountain Lab from Fauci’s Monkey Island in South Carolina, infect them with viruses including Ebola and COVID, and then completely withhold pain relief while the animals suffer excruciating deaths.

'Taxpayers have a right to know how their money is being spent in barbaric NIH animal labs that can cause a devastating lab leak and pandemic right here in the US.'

https://www.dailymail.co.uk/health/article-13008119/montana-lab-scientists-experimenting-dangerous-pathogens.html

Snake Venom Key Ingredient In “Covid-19 Vaccine” Patents
April 14, 2022 by Dr. Ariyana Love
By Dr. Ariyana Love, ND

The world premier documentary Watch The Water aired on Red Voice Media this week. Dr. Bryan Ardis dropped a bombshell during his interview with Stew Peters about one of the greatest conspiracy truths of all time. The intentional poisoning of the world’s population through our municipal water supply using snake venom.

Please see: VenomTech company announces massive library of SNAKE VENOM peptides for pharmaceutical development; “nanocarriers” stabilize snake venom in WATER (PubMed)

SNAKE VENOM PATENTS

Most snake venoms contain proteolytic enzymes. I found Snake venom in ten Covid-19 vaccine patents listed as “venom” and “proteolytic” (enzyme).

Snake venom is being recently touted as an “anti-HIV” drug, since January 2022. There’s six PLA2s from Snake Venoms patents “against HIV”. These synthetically derived snake venoms are marketed under the guise of being “antiviral” and as a preventive treatment for HIV infection.

The study claims snake venom works to “protect against Lentiviruses” through the “destruction of the viral membrane.” However, this is a lie because we know the Lentiviruses are a lab generated, chimeric mRNA bioweapon containing SARS, MERS, HIV 1-3 and SRV-1 (AIDS), as I documented in my article entitled, Transgenic Hydras & Parasites A Biological Weapons System For Rapid Human Cloning.

In actuality, snake venom is being used to destroy the human cell membrane not the “viral membrane”, so that nanoparticles can enter the cell and code your genome. This PubMed study proves that HIV is being encoded into people’s cells to produce a new cell line persistently. So snake venom assists mRNA to clone your cells. The J&J patent also mentions “RNA Replicons” which are forever replicating proteins.

Our Satanic “elites” have programmed the AI to create bioweapons far more complex than humans could ever come up with and the AI came up with 40,000 of the most deadly bioweapons to date.

THE SPIKE PROTEIN

The ACE2 protein acts as an anti-inflammatory, keeping immune cells from inflicting damage on the body’s own cells. The ACE2 receptor helps muscles contract and acts as a messenger between nerves, muscles and cells. It’s crucial in your cell signaling processes.

The ACE2 molecule acts as a gateway, preventing toxins from entering your cells. The mainstream narrative says that SARS-CoV-2 or the “spike protein”, attaches to human cells and blocks the ACE2 receptors. Snake venoms are postsynaptic neurotoxins, meaning they block the Ace2 receptors. So, I think we’ve identified the “spike protein”.

Snake venom latches onto ACE2 proteins and they get knocked out of commission. This destroys the body’s cell signaling function and enables the nanotech weapons system to enter the cells and reach the nucleus, where the mRNA is reverse-transcribed and integrated into the human genome.

Snake venom causes paralysis, the loss of muscle function and respiratory failure. It also causes inflammation, cytokine storms and induces auto-immune illness. Studies say snake venom triggers irreversible intracellular alterations, organ failure and continued cell death.

Heart and lung cells are covered with these ACE2 surface proteins which could explain why there’s so many reports of acute Myocardial injury following “Covid-19 vaccination”. I am receiving a lot of reports from my clients of prolonged stomach pain from these lethal jabs, another causation of snake venom which affects your digestion.

Speaking of digestion, the Food and Agriculture Organization of the US approved the use of snake venom in food last year (2021). According to the FAO/WHO the PLA2 enzyme (snake venom) complies with the General Specifications and Considerations for Enzyme Preparations Used in Food Processing. They’re using a combination of snake venom and a genetically modified Streptomyces violaceoruber bacteria (strain pChi). In other words, it will alter your genome.

Notice the conflict of interest in this safety study that declares the pChi strain is not harmful for consumption. The study does admit that this bacterial strain modifies your genome. I don’t believe that any level of genetic modification of humans is at all safe.

CROTOXIN

60% of snake venom consists of a neurotoxic substance called Crotoxin. It was the first proteinic toxin to be crystallized into protein crystallization. Once crystallized it can be used in structural biology. You can even buy Crotoxin online.

ORGANOIDS

Organoids are being grown a lab to mass produce snake venom. Organoids of snake glands can produce snake venom artificially, without the entire snake.

MONOCLONAL ANTIBODIES

Monoclonal antibodies were funded and developed by DARPA and Bill Gates. All monoclonal antibody patents reveal this is a mRNA “vaccine” that codes your cells with HIV-1. Just like the “Covid-19 vaccines”, monoclonal antibodies never underwent clinical safety trials. They’ve never been approved for use on humans and were passed under the Emergency Use Authorization.

In his interview with Mike Adams, Dr. Bryan Ardis mentioned a study funded by Fauci and the NIH that proved monoclonal antibodies are in fact, unsafe. They specifically target and destroy your T-cells (killer cells) through cytotoxicity. Thermo Fisher’s monoclonal antibodies actually contain snake venom (PLA2)!

Please read: Monoclonal Antibodies Is Experimental Gene Therapy – Patent Review

All monoclonal antibodies contain Hydroxychloroquine or chloroquine in “some embodiments”. This explains why some people report feeling better after using monoclonal antibodies at first and that’s enough to fool doctors but later they become extremely fatigued. The long-term effects are still unknown but they cannot be good. When your immune system is destroyed, your body cannot fight off disease.

NANOBODIES

The Oxford patent mentions “Nanobodies” and says that “antibodies have been replaced with Nanobodies”. The whole purpose of the “Covid-19 vaccines” was to invoke an “antibody response”. Now that lie too is exposed. The nanotechnology is being programmed to kill.

ANTIDOTE

There are breakthrough medicines and supplements that work antidotally against all poisons, including snake venom. In the Dr. Bryan Ardis interview with Dr. Braun, he mentioned the power of redox molecules against snake poison.

A peer-reviewed study from 2018, shows that Melatonin inhibits snake venom and antivenom induced oxidative stress:

“Besides antibodies, molecules like melatonin are reported to underlie the antivenom effect. The study of such was established in Egyptian cobra (Naja haje) venom using a rat model; the vital organs, like kidney, liver and heart, of the rat were protected from the venomous effect.”

Contact me on Telegram for information on where you can obtain the redox molecule supplement that enables your body to remove all poisons and restores all of your body system functions.

Also, follow my Telegram channel here.

Watch my latest interview with Stew Peters at Red Voice Media, here.

Here's the synthetic snake venom patents I documented and found in the Covid-19 vaccines.

https://ambassadorlove.blog/2022/04/14/snake-venom-key-ingredient-in-covid-19-vaccine-patents/

WEF Admits Disease X Will Be Leaked in 2025
Sean Adl-Tabatabai
Fact checked
January 23, 2024 30 Comments
WEF admits Disease X will be unleashed in 2025.
The World Economic Forum (WEF) has declared that ‘Disease X’ will be unleashed onto the public by the year 2025 – and the consequences will be devastating for humanity.



Last week, global elites met at the WEF Davos summit where the key topic of discussion was “Preparing for Disease X,”1 a hypothetical new deadly pandemic predicted to emerge in 2025 and kill 20 times more people than COVID-19.2 As reported by the Mirror:3



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“The World Health Organization (WHO) has warned of a potential Disease X since 2017, a term indicating an unknown pathogen that could cause a serious international epidemic …

Public speakers at the ‘Preparing for Disease X’ event next Wednesday [January 17, 2024] include Tedros Adhanom Ghebreyesus, director-general of the WHO, Brazilian minister of health Nisia Trindade Lima, and Michel Demaré, chair of the board at AstraZeneca.

In their first post-pandemic meeting held in November 2022, the WHO brought over 300 scientists to consider which of over 25 virus families and bacteria could potentially create another pandemic.

The list the team came up with included: the Ebola virus, the Marburg virus disease, Covid-19, SARS, and the Middle East respiratory syndrome coronavirus (MERS-CoV). Others included lassa fever, nipah and henipaviral diseases, zift Valley fever, and zika — as well as the unknown pathogen that would cause ‘Disease X.’”

Mercola.com reports: I’ve interviewed Meryl Nass about how the WHO is trying to take over aspects of everyone’s lives. She just published an important piece over the weekend, Why Is Davos So Interested in Disease? about how the WEF and the WHO have become partners to terrify the world.

Alexis Baden-Mayer, Esq., political director for the Organic Consumers Association, did some digging into the participants of this WEF event, and the two things they all have in common are 1) dumping the AstraZeneca COVID shot on the developing world (primarily India and Brazil) after rich countries rejected it due to its admitted blood clotting risk, and 2) pushing for the implementation of medical AI systems that will eliminate doctors along with patient choice and privacy.

Practice Runs or Responsible Planning?

In a January 11, 2024, tweet, Fox News analyst and former assistant secretary for public affairs for the U.S. Treasury Department, Monica Crowley, wrote:4

“From the same people who brought you COVID-19 now comes Disease X: Next week in Davos, the unelected globalists at the World Economic Forum will hold a panel on a future pandemic 20x deadlier than COVID …

Just in time for the election, a new contagion to allow them to implement a new WHO treaty, lock down again, restrict free speech and destroy more freedoms. Sound far-fetched? So did what happened in 2020. When your enemies tell you what they’re planning and what they’re planning FOR, believe them. And get ready.”

Dr. Stuart Ray, vice chair of medicine for data integrity and analytics at Johns Hopkins’ Department of Medicine, dismissed such warnings, telling Fortune magazine5 that “Coordination of public health response is not conspiracy, it’s simply responsible planning.”

I’d be willing to believe him if it wasn’t for a now-obvious trend: Whatever the globalists claim will happen actually does happen at a remarkable frequency, and their prognostic capabilities become easier to explain when you consider that most lethal pandemics have been caused by manmade viruses, the products of gain-of-function research. It’s pretty easy to predict a new viral outbreak if you have said virus waiting in the wings.

With that in mind, recent research from China certainly raises concern, to say the least. According to a January 3, 2024, preprint,6 a SARS-CoV-2-related pangolin coronavirus — described as a “cell culture-adapted mutant” called GX_P2V that was first cultured in 2017 — was found to kill 100% of the humanized mice (ACE2-transgenic mice) infected with it.7

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The primary cause of death was brain inflammation. According to the authors, “this is the first report showing that a SARS-CoV-2-related pangolin coronavirus can cause 100% mortality in hACE2 mice, suggesting a risk for GX_P2V to spill over into humans.”

However, if this virus mutated as a result of passaging through cell cultures, then it’s not likely to emerge in the wild. It’s another unnatural lab creation, so rather than saying it may spill over from pangolins to humans, it would be more accurate to admit that it may pose a (rather serious) risk to humans were a lab escape to occur.

COVID Dress Rehearsals

In 2017, Johns Hopkins Center of Health Security held a coronavirus pandemic simulation called the SPARS Pandemic 2025-2028 scenario.8 Importantly, the exercise stressed “communication dilemmas concerning medical countermeasures that could plausibly emerge” in a pandemic scenario.

Then, in October 2019, less than three months before the COVID-19 outbreak, the Bill & Melinda Gates Foundation in collaboration with Johns Hopkins and the World Economic Forum hosted Event 201.

The name itself suggests it may have been a continuation of the SPARS Pandemic exercise. College courses are numbered based on their prerequisites. A 101 course does not require any prior knowledge whereas 201 courses require prior familiarity with the topic at hand.

As in the SPARS Pandemic scenario, Event 201 involved an outbreak of a highly infectious coronavirus, and the primary (if not sole) focus of the exercise was, again, how to control information and keep “misinformation” in check, not how to effectively discover and share remedies.

Social media censorship played a prominent role in the Event 201 plan, and in the real-world events of 2020 through the present, accurate information about vaccine development, production and injury has indeed been effectively suppressed around the world, thanks to social media companies and Google’s censoring of opposing viewpoints.

In March 2021, an outbreak of “an unusual strain of monkeypox virus” was simulated.9 In late July the following year, the WHO director-general declared that a multi-country outbreak of monkeypox constituted a public health emergency of international concern,10 against his own advisory group.

‘Catastrophic Contagion’ Exercise

Considering both of these simulations, SPARS (“Event 101”?) and Event 201, foreshadowed what eventually occurred in real life during COVID, when Gates hosts yet another pandemic exercise, it’s worth paying attention to the details.

October 23, 2022, Gates, Johns Hopkins and the WHO cohosted “a global challenge exercise” dubbed “Catastrophic Contagion,”11,12 involving a fictional pathogen called “severe epidemic enterovirus respiratory syndrome 2025” (SEERS-25).

Enterovirus D6813 is typically associated with cold and flu-like illness in infants, children and teens. In rare cases, it’s also been known to cause viral meningitis and acute flaccid myelitis, a neurological condition resulting in muscle weakness and loss of reflexes in one or more extremities.

Enteroviruses A71 and A6 are known to cause hand, foot and mouth disease,14 while poliovirus, the prototypical enterovirus, causes polio (poliomyelitis), a potentially life-threatening type of paralysis that primarily affects children under age 5. So, the virus they modeled in this simulation appears to be something similar to enterovirus D68, but worse.

Vaccine Drug Trials Begin for Deadly Nipah Virus

One known virus that bears some resemblance to the fictional SEERS-25 is the Nipah virus. This virus has a kill rate of about 75%,15 and survivors oftentimes face long-term neurological issues stemming from the infection. Nipah is also said to affect children to a greater degree than adults.16

Incidentally, human trials for a vaccine against the deadly Nipah virus were recently launched.17 Volunteers received their first shots in early January 2024. The experimental injection uses the same viral vector technology used to produce AstraZeneca’s COVID shot.

The trial is reportedly being carried out by the University of Oxford in an undisclosed area where Nipah is actively infecting victims. (India seems to be indicated, as an outbreak in Kerala killed two people and hospitalized three in September 2023.18)

The disease is thought to spread via interaction with infected animals such as goats, pigs, cats and horses. It may also spread via tainted blood products and food. Symptoms can emerge anywhere from a few days after exposure to as long as 45 days.

Initial symptoms include fever, headache and respiratory illness, which can rapidly progress to encephalitis (brain swelling), seizures and coma within just a couple of days. According to the WHO, pigs are known to be “highly contagious” during the incubation period, and it’s possible that humans may be as well, although that has yet to be confirmed.

Training African Leaders to Go Along With the Narrative

Tellingly, the Catastrophic Contagion exercise focused on getting leadership in African countries involved and trained in following the script. African nations went “off script” more often than others during the COVID pandemic, and didn’t follow in the footsteps of developed nations when it came to pushing the jabs.

As a result, vaccine makers now face the problem of having a huge control group, as the COVID jab uptake on the African continent was only 6%,19 yet it fared far better than developed nations in terms of COVID-19 infections and related deaths.20

The Catastrophic Contagion exercise predicts SEERS-25 will kill 20 million people worldwide, including 15 million children, and many who survive the infection will be left with paralysis and/or brain damage. In other words, the “cue” given is that the next pandemic may target children rather than the elderly, as was the case with COVID-19.

Vaccine Against Unknown ‘X’ Pathogen Is Already in the Works


In August 2023, a new vaccine research facility was set up in Wiltshire, England, fully staffed with more 200 scientists, to begin work on a vaccine against the unknown “Disease X.” As reported by Metro:21

“It took 362 days to develop the Covid-19 vaccine. But the Vaccine Development and Evaluation Centre team wants to reduce that time to 100 days. Scientists at the facility will develop a range of prototype vaccines and tests.

The new lab is a part of a global effort to respond to global health threats. The UK and other G7 countries signed up to the ‘100 Days Mission’ in 2021. The government has invested £65 million into the lab.

Professor Dame Jenny Harries, the head of the UK Health Security Agency, said the new facility would ‘ensure that we prepare so that if we have a new Disease X, a new pathogen, we have as much of that work in advance as possible.’”

In the U.S., Congress also introduced the “Disease X Act of 2023” (H.R.383222) back in June 2023. The bill calls for the establishment of a BARDA program to develop “medical countermeasures for viral threats with pandemic potential.” The bill was referred to the Subcommittee on Health in early June 2023 but has not yet been passed.

The Disease X Act amends a section of the Public Health Service Act with two new clauses that call for “the identification and development of platform manufacturing technologies needed for advanced development and manufacturing of medical countermeasures for viral families which have significant potential to cause a pandemic,” and “advanced research and development of flexible medical countermeasures against priority respiratory virus families and other respiratory viral pathogens with a significant potential to cause a pandemic, with both pathogen-specific and pathogen-agnostic approaches …”

Needless to say, since it’s impossible to customize vaccines using the conventional method of growing viruses in eggs or some other cell media in 100 days, it seems inevitable that all these efforts are about the expansion of gene-based technologies. This, despite the fact that the mRNA technology used for the COVID jabs has proven to be disastrous from a safety standpoint, and ineffective to boot.

Why Manufactured Pandemics Will Continue

At this point, it’s quite clear that “biosecurity” is the chosen means by which the globalist cabal intends to seize power over the world. The WHO is working on securing sole power over pandemic response globally through its international pandemic treaty which, if implemented, will eradicate the sovereignty of all member nations.

The WHO’s pandemic treaty is the gateway to a global, top-down totalitarian regime, a one world government. Ultimately, the WHO intends to dictate all health care. But to secure that power, they will need more pandemics. COVID-19 alone was not enough to get everyone onboard with a centralized pandemic response unit, and they probably knew that from the start.

So, the reason we can be sure there will be additional pandemics, whether manufactured using either fear and hype alone or an actual bioweapon created for this very purpose, is because the takeover plan, aka The Great Reset, is based on the premise that we need global biosecurity surveillance and centralized response.

Biosecurity, in turn, is the justification for an international vaccine passport, which the G20 has signed on to, and that passport will also be your digital identification. That digital ID, then, will be tied to your social credit score, personal carbon footprint tracker, medical records, educational records, work records, social media presence, purchase records, your bank accounts and a programmable central bank digital currency (CBDC).

Once all these pieces are fully connected, you’ll be in a digital prison, and the ruling cabal — whether officially a one world government by then or not — will have total control over your life from cradle to grave.

We’re Already Suffering Under a Pseudo-One World Government

We actually already have a pseudo-one world government, in the form of Bill Gates’ nongovernmental organizations (NGOs). They are making health care decisions that should be left to individual nations and/or states, and they’re making decisions that will line their own pockets, regardless of what happens to the public health-wise.

They coordinate and synchronize pandemic communication during simulated practice runs, and then, when the real-world situation emerges that fits the bill, the preplanned script is played out more or less verbatim.

Between the G20 declaration to implement an international vaccine passport under the auspice of the WHO, and the WHO’s pandemic treaty, everything is lined up to take control of the next pandemic, and in so doing, further securing the foundation for a one world government.

As discussed in my 2021 article, “COVID-19 Dress Rehearsals and Proof of the Plan,” the pandemic measures rolled out for COVID-19 were the culmination of decades of careful planning to radically and permanently alter the governance and social structures of the world.

The medical system has been used in the past to drive forward a New World Order agenda — now rebranded as “The Great Reset” — and it’s now being used to implement the final stages of that longstanding plan. COVID-19 was a real-world practice run, and showed just how effectively a pandemic can be used to shift the balance of power, and strip the global population of its wealth and individual freedoms.

So, there’s no doubt in my mind that additional pandemics will be declared, because they’re the means to the globalists’ ends. To prevent this global coup, we need everyone to speak and share the truth to the point that you’re able. Only then will our voices outnumber the voices of the propaganda machine.

Door To Freedom (doortofreedom.org), an organization founded by Dr. Meryl Nass, has a poster that explains how the pandemic treaty and International Health Regulations (IHR) amendments will change life as we know it and strip us of every vestige of freedom. Please download this poster and share it with everyone you know. Also put it up on public billboards and places where communities share information.

Not only a healthy way to eat but also the most sustainable, eating nose to tail provides you with some of the most nutritionally dense sources of valuable minerals and fat-soluble vitamins from organ meats. Help balance the nutritional shortcomings of muscle meats with Grass Fed Beef Organ Complex, offering five of the most valuable organs — liver, heart, kidney, pancreas and spleen — from roaming, healthy New Zealand cows with year-round access to grasslands.

1, 21 Metro January 15, 2024
2, 3 Mirror January 13, 2024
4 Twitter/X Monica Crowley January 11, 2024
5 Fortune January 12, 2024
6 ResearchGate January 2024 DOI: 10.1101/2024.01.03.574008
7 MSN January 15, 2024
8 SPARS Pandemic Scenario
9 NTI Paper November 2021
10 UN News July 23, 2022
11 Catastrophic Contagion
12 Catastrophic Contagion Videos
13 CDC Enterovirus D68
14 CDC Enteroviruses
15 Forbes September 15, 2023
16 Intractable & Rare Diseases Research February 2019; 8(1): 1-8
17 Forbes January 11, 2024
18 BBC September 14, 2023
19 First Post November 19, 2021
20 Yahoo News November 19, 2021
22 HR 3832 The Disease X Act of 2023

https://thepeoplesvoice.tv/wef-admits-disease-x-will-be-leaked-in-2025/

Chinese Scientists Create COVID Strain That’s 100% Lethal in ‘Humanized’ Mice
Scientists at the Beijing University of Chemical Technology created a mutated pangolin coronavirus capable of replicating in the lung and brain tissue of genetically engineered mice and killing the mice within eight days. Critics of the study questioned the value of what they called a high-risk gain-of-function experiment.

John-Michael Dumais
pangolin covid strain lethal mice feature
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Chinese scientists have created a mutated pangolin coronavirus that is 100% lethal in “humanized” mice, raising biosafety concerns around risky gain-of-function research.

The preprint study demonstrated the virus’ ability to replicate in lung and brain tissue, concluding that severe neurological infection likely caused the mice’s deaths.

According to scientists at the Beijing University of Chemical Technology, the SARS-CoV-2-related pangolin variant “GX_P2V C7” was derived from a previously cloned virus that mutated in lab-grown cell cultures.

When intranasally inoculated into mice bioengineered to express human ACE2 receptors, the virus killed all of the mice within eight days.

The researchers warned their finding “underscores a spillover risk of GX_P2V into humans” and concluded that this research could provide an alternative model for investigating the pathogenic mechanisms of emerging coronaviruses.

Dr. Marty Makary, Johns Hopkins professor of surgery and author of “The Price We Pay: What Broke American Health Care — and How to Fix It,” took to X (formerly known as Twitter) to comment on the study:

Dr. James Thorp, whose medical experience includes 44 years in obstetrics and fetal maternal medicine, and the author of more than 245 scientific papers, wrote on X, “Sure appears like a lab-created bioweapon to me. Am I missing something? Do you believe that this research is being done for the good of humanity? Have we collectively gone insane?”

Many on X wondered whether this kind of research would result in the outbreak of the theoretical “Disease X” predicted by the World Health Organization, the World Economic Forum, the Bill & Melinda Gates Foundation, the Coalition for Epidemic Preparedness Innovations and other globalist organizations.

Chinese study ‘scientifically totally pointless’

Francois Balloux, Ph.D., chair in Computational Biology Systems Biology at University College London, responded to the study with the following tweet:

Richard Ebright, Ph.D., professor of chemistry and chemical biology at Rutgers University, told The Defender he agreed with Professor Balloux’s assessment:

“I note that the preprint does not specify the biosafety level and biosafety precautions used for the research. … The absence of this information raises the concerning possibility that part or all of this research, like the research in Wuhan in 2016-2019 that likely caused the COVID-19 pandemic, was recklessly performed without the minimal biosafety protections essential for research with a potential pandemic pathogen.”

The Chinese paper comes on the heels of a recent study documenting the escape of 16 pathogens from biosafety laboratories between 2000 and 2021, which resulted in at least 316 infections and eight deaths — not including the global impact of the likely leak of SARS-CoV-2.

Ebright noted that while China took steps to strengthen biosafety regulations after the COVID-19 disaster, the U.S. did not, “due to opposition and obstruction by [Dr. Anthony] Fauci and [Dr. Francis] Collins.” Collins is the former director of the National Institutes of Health (NIH).

“I am surprised that high-risk, low-value research, such as the research in this preprint, continues in China today, likely with inadequate biosafety protections, even after the strengthening of biosafety regulations,” Ebright said.

Brian Hooker, Ph.D., senior director of science and research at Children’s Health Defense, told The Defender that he agreed with Ebright’s concern about the lack of biosafety documentation accompanying the study, and said this type of research is “extremely dangerous given the potential for lab leaks or other catastrophes.”

“The investigators claim that this is not gain-of-function research — that is simply not true,” Hooker said. “Given the high level of mutation of these RNA viruses, the mere experimentation involving the eight infected, humanized mice could select for mutations that interact more robustly with the human ACE2 receptor.”

Christina Parks, Ph.D., a science educator with a degree in cellular and molecular biology, posted a video about the study, saying, “This is gain-of-function research. There’s no two ways about it.”

“This particular variant is not causing lung infection [in the mice], it’s destroying their brains in a matter of hours and days, and causing 100% lethality. … and not just any mice, mice that have been [engineered] to be more like humans,” she said.

Justin Kinney, Ph.D., co-founder of Biosafety Now, an organization that seeks tighter regulations for gain-of-function research, told The Epoch Times the research described in the paper was not technically gain-of-function “because the China-based scientists did not purposely enhance the virus to be more pathogenic or transmissible.”

“The research is still very dangerous,” Kinney said. He also expressed concern that the paper did not identify the biosafety level at which the work was performed.

Kinney, who also serves as associate professor of quantitative biology at Cold Spring Harbor Laboratory in New York, on Jan. 10 testified in the Wisconsin State Assembly in favor of a bill that would prohibit gain-of-function research that enhances potential pandemic pathogens and would require researchers to file reports with state and local officials.

Hooker raised concerns about the potential military applications of the research. “There are also links to the effort in the Chinese military where offensive bioweapons can be developed,” he said.

One of the study’s authors, Yigang Tong, was trained by the Chinese military, worked in military-run labs and co-authored a 2023 paper with Shi Zhengli, a senior scientist at the Wuhan Institute of Virology (WIV) also about a pangolin virus infecting transgenic mice.

University of Illinois international law professor Francis Boyle, J.D., Ph.D., a bioweapons expert who drafted the Biological Weapons Anti-Terrorism Act of 1989, told The Defender the Chinese study looked to him like “a biowarfare arms race between PRC [People’s Republic of China] and USA.”

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Humanized mice and the ACE2 receptor

In the Chinese study, the mice were genetically engineered to produce human ACE2 receptors.

ACE2 — short for angiotensin-converting enzyme 2 — is a protein found on the surface of many human cells, especially those in the lungs, blood vessels, heart, kidney and gastrointestinal tract.

The ACE2 receptor acts as the entry point for SARS-CoV-2, the virus that causes COVID-19, to get into cells and start infection. The spike protein on the surface of the coronavirus directly binds to ACE2 receptors, allowing the virus access into the host cell where it can replicate.

In the Chinese study, testing verified the presence of viral antigens spreading in both the pulmonary and cerebral regions over time. However, the findings showed largely an absence of major inflammatory responses or tissue damage.

While lung viral titers decreased by day six post-infection in the humanized mice, the study reported “exceptionally high” genome copies in neural tissue, signaling lethal neurological invasion.

Quantitative testing identified significant viral loads across organ systems, but most notably in the brain.

The infected mice additionally displayed symptoms like sluggishness, white eyes, 10% weight loss and ruffled fur shortly before death.

In records obtained by Judicial Watch through a Freedom of Information Act request in 2021, a proposal by EcoHealth Alliance described a plan to sequence the spike protein at the WIV from bat coronaviruses for the purpose of “creating mutants to identify how significantly each would need to evolve to use ACE2.”

EcoHealth Alliance received a $3.3 million grant from NIH for a project called “Understanding the Risk of Coronavirus Emergence” that ran at the WIV from 2013 through 2018.

The research involved infecting “humanized” mice with SARS-like coronaviruses.

Boyle, in a recent interview with The Defender, said that he believed the SARS-CoV-2 virus was developed through gain-of-function research to be an offensive biological warfare weapon before it leaked out of the WIV lab.

Boyle said that labs doing this kind of work anywhere in the world “must be shut down immediately before we have another COVID-19 pandemic.”

Chinese Scientists Create COVID Strain That’s 100% Lethal in ‘Humanized’ Mice

“Sure appears like a lab-created bioweapon to me. Am I missing something? Do you believe that this research is being done for the good of humanity? Have we collectively gone insane?” — Dr. James Thorp



https://childrenshealthdefense.org/defender/beijing-scientists-pangolin-covid-variant-lethal-mice/

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Japan's CBC News, January 19, 2024.

Look at all the teenagers with suspected post vaccination serious adverse events in Japan!!

Highlights--------------------------
There have been 36,714 reports of suspected adverse reactions after vaccination. This number exceeds 36,714. Among these, there are 2,122 reports of suspected deaths after vaccination. Among these, there are only 2 cases where causation cannot be denied.

Most of them are "unassessable". The reason for being unassessable, according to the Ministry of Health, Labor and Welfare, is insufficient information.

How many cases of compensation have been accepted for the new coronavirus vaccine? The number is 9,910. However, applying for the relief system requires a tremendous amount of documentation. For some people, they need to gather more than 1,000 documents. Gathering over 1,000 documents while unwell is truly challenging and has a high hurdle. Therefore, many people have not even applied.

- A 9-year-old boy. The disease name or disability name is Nephrotic Syndrome, Both anal cancer, and central cancer with stone-colored pigmentation. Nephrotic Syndrome is a condition where a lot of protein is excreted in the urine. The protein in the blood may decrease. There can also be swelling in the body. In some cases, this can lead to kidney failure or thrombosis. Thrombosis can potentially cause heart attacks or strokes. And anal cancer is a condition where the pressure in both eyes rapidly increases, resulting in symptoms such as eye pain, nausea, and headaches.

- This is a boy who received vaccinations at the age of 17 and 18. It means he received two doses. Encephalitis (Brain Inflammation), convulsion assistance. Encephalitis can cause fever, headache, and seizures after vaccination. Convulsion assistance involves losing consciousness and experiencing seizures.

- A 17-year-old girl. Glandular pain syndrome. The pain from glandular pain syndrome has worsened.

- And the boy who received shots at the ages of 15 and 16 has peripheral nerve damage and weakness. Also, dysesthesia, numbness in both hands and feet, and head. Now, this is quite noteworthy.

- A boy at the ages of 15 and 18, acute myocarditis and acute pericarditis. Teenage boys, young men in their early twenties are said to be prone to myocarditis and pericarditis. This boy is experiencing symptoms of both myocarditis and pericarditis.

-And here is a 10-year-old girl. Alopecia areata onset. So, maybe she had alopecia areata originally. However, the symptoms reappeared after vaccination. Let's take a look at the next page. This is a single case.

-A 15-year-old girl. Headache, abdominal pain, diarrhea, fatigue, loss of appetite, numbness in both hands and feet, and hypersensitivity to auditory stimuli. The symptoms are diverse. This is also a characteristic example of post-vaccination effects. Now, here is another case.

-A 17-year-old girl. Bilateral leg weakness and continued weakness in the entire body.

-A 15-year-old girl. Fever, fatigue, joint pain, pain in both legs, numbness, walking difficulties, and continued depressive state. Among the people I interviewed, some have even experienced a deterioration in their mental state. And this is the last page.

-A 14-year-old girl. Headache, visual impairment.

-And an 18-year-old male. This is related to vasospastic angina. Temporary strong contractions caused by spasms in the coronary arteries. And poor blood flow to the heart muscle. Due to spasms and constriction of blood vessels, blood flow is impaired, leading to angina.

Children under 10 and teenagers are suffering from these symptoms.
---------------------------
H/T:@You3_JP

https://x.com/_aussie17/status/1748559029620846597?s=46&t=BnqCjhlm68VHjRNptPlFjA

Israel's skin bank raises ethical concerns on organ consent
Jordan News last updated: Nov 17,2023
gaza
(Photo: Twitter/X)
GAZA – Israel possesses the world's largest skin bank, a medical facility that stores human skin for later use in treating burns and skin cancers. This bank was established in 1986 under the supervision of the military medical sector of the occupying army, which provides its services internationally, especially to requests from Western countries.

Israeli occupation authorities been stealing organs from the bodies of dead Palestinian, a heinous criminal practice that has been revealed in several reports and through testimonies of Israeli doctors who participated in this gruesome practice, violating professional ethics and constituting a crime against humanity, Al-Ghad reported.

In contrast, this Israeli bank differs from other banks worldwide in that its supply of these vital organs does not come solely from voluntary donors. Instead, documented cases of stealing skin from the bodies of Palestinians have been recorded, individuals whose organs are also stolen.

There is compelling evidence of Israelis engaging in trafficking these stolen organs, making the entity the largest market for organs in the Middle East.

Where did Israel get this inventory from?
Expert in Israeli affairs Anas Abu Arqoub says, "The Israeli skin bank is the largest in the world, surpassing the American skin bank that was established 40 years before it, noting that Israel's population is much smaller than the United States."

Arqoub emphasizes that the theft of organs from Palestinian bodies is not just suspicions, stating, "Even the Israeli media acknowledges that it is an extraction process without the knowledge of the dead's families."

The reserve of human skin held by the Israeli occupation state, equivalent to 170 square meters, stored within the Israeli skin bank, confirms Arqoub's account. The number is considered unreasonable since Israel ranks third in its population's refusal to donate organs, attributed to Jewish religious beliefs.

Handing over Palestinian bodies to their families without organs!
The details of the story date back to 2001 when Swedish investigative journalist Donald Boström published an investigation exposing the theft of organs from the bodies of Palestinian martyrs and their trafficking by Israeli entities. This was the first time this crime was revealed to the international public.

Boström did not stop at this point but published another investigation on the same subject in 2009 in the pages of the Swedish magazine "Aftonbladet." The investigation mentions that the Israeli Ministry of Health launched a national campaign to encourage organ donation in 1992. However, despite that, a significant gap persisted between the demand and the supply of donations.

Coinciding with that campaign, cases of the disappearance of several Palestinian youth began, only to return afterward in closed coffins. The Israeli authorities imposed on their families to bury them at night without funerals.

Boström says, "I was in the region at that time, and on several occasions, UN employees contacted me concerned about the developments. The individuals who contacted me said that organ theft certainly happened, but they were prevented from doing anything about it."

These contacts prompted the journalist to delve further into the issue, so he went to interview the families of the dead who confirmed the theft of their sons' organs before their killing. Among them was the son of the martyr Bilal Ahmed Ghannan, who was 19 years old when the Israeli army arrested him in the village of Um al-Tut in the West Bank in 1992. He returned with a body without internal organs, from the neck to below the abdomen.

The Israeli medical authorities did not deny the torture and theft of Bilal's organs. At that time, the director of the Israeli Institute of Forensic Medicine, Chen Kugel, said that Bilal's family could be right because they "took everything that could be taken from all the bodies that came to the Institute of Forensic Medicine," without the family's consent. His family did not receive any explanation, apology, or compensation for what happened.

Israeli confessions of organ theft from Palestinians
In a 2009 documentary on the issue, there are admissions from the former director of the Israeli Institute of Forensic Medicine, Yehuda Hiss, confirming the theft of organs from the bodies of Palestinian in the institute. Hiss stated, "We took corneas, skin, heart valves, and bones ... Almost everything was done unofficially to a large extent... and permission was not sought from the families."

In her study on dealing with the bodies of Palestinians at the Abu Kabir Forensic Medicine Center in Tel Aviv, published in a book titled "On Their Bodies," anthropologist Meirav Feis stated that she witnessed "how they take organs from the bodies of Palestinians. In return, they leave the bodies of soldiers intact."

The researcher added, "They take corneas, skin, and heart valves in a way that makes the absence of those organs unnoticed by non-specialists. They replace corneas with plastic bodies and remove the skin from the back so that the family does not see it. In addition, the bodies of the dead are used in medical schools in Israeli universities for research purposes."

Feis said, "In the first intifada, the army effectively allowed the institute to extract organs from Palestinians under a military procedure that required dissecting the bodies of Palestinian prisoners. The autopsy procedure was accompanied by the removal of organs used by the Israeli skin bank, established in 1985 to treat burns suffered by Israeli soldiers."

Trafficking in the organs of Palestinian casualties
Israel is one of the largest markets for trafficking in human organs in the world, and the largest in the Middle East. Media reports revealed that the Israeli entity is involved in killing Palestinians to steal their internal organs illegally and trade them within an illegal international network.

In 2009, the US Federal Bureau of Investigation (FBI) arrested an Israeli settler named Levy Izhak Rosenbaum. After investigating him, it was revealed that he played the role of a broker in organ-selling operations in the United States for the benefit of a criminal cell led by rabbis, politicians, and government officials in Israel.

Journalist Donald Boström, in his mentioned investigation, suggests a connection between this network and the theft of organs from Palestinian martyrs taking place in "Israel." Boström said, "Half of the kidneys transplanted to Israelis since the beginning of the first decade of the 21st century were illegally purchased. The Israeli health authorities have full knowledge of this activity but do nothing to stop it."

In a report published by the Israeli newspaper "Haaretz" in 2016, Israel admitted to losing dozens of bodies of Palestinians. The newspaper quoted statements from sources in the Israeli judicial and security apparatuses about the loss of 121 bodies of Palestinians held by the occupation authorities since the 1990s.

Continued organ theft Following the explosion of the organ theft scandal in 2009, the Israeli government tried to evade the proven charges against it. The spokesperson for the Israeli Ministry of Health at that time, Einav Shimron Greenboim, issued a statement saying, "The practice mentioned in the investigation is an old story that ended years ago."

Doubts persist about the continuation of these unethical practices that violate human rights, as indicated by the Israeli authorities' continued detention of dozens of bodies of Palestinian dead, justifying it as a punitive measure.

According to Abdel Nasser Farwana, the head of the Studies and Documentation Unit at the Palestinian Prisoners and Ex-Prisoners Affairs Commission, Israel still holds more than 370 bodies of Palestinian and Arab bodies who died in different circumstances and years apart. He added, "The list of these detained martyrs includes individuals who died from the 1970s until around 2023."


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https://www.jordannews.jo/Section-20/Middle-East/Israel-s-skin-bank-raises-ethical-concerns-on-organ-consent-32381