Pfizer partnering with Ido Bachelet on DNA nanorobots
OUTRAGED HUMAN
“No, no it’s not science fiction; it’s already happening,” said Ido Bachelet to a somewhat incredulous audience member








https://www.youtube.com/watch?v=MzLTWU2EqP4 Ido Bachelet - Moonshot Thinking


... when they cause too much damage by mistake...

or intentionally...


5:12

study your biology and activate targeted medication when necessary.


5:36

We also know how to remote-control these robots, using magnetic fields.

5:40

Furthermore, we can control them, as you saw in the clip, with a joystick,

5:43

directing them to a specific part of the body,

5:46

and then activating them with the push of a button.

5:49

We have also connected this joystick to the internet.

5:51

Our robots have a IP address,

5:54

so you can connect with them from afar and activate them online.



6:01

Imagine that in a couple of years,

6:03

your doctor will be able to sit at home with his smartphone,

6:05

and instead of playing "Candy Crush"

6:08

he will connect with the robots inside of you,

6:11

activate a certain medication and possibly even save you, just in time.

AND IMAGINE THAT YOU WOULDN'T EVEN KNOW IT, YOU WOULDN'T BE TOLD ABOUT IT.

AND THAT IN ORDER TO IMPLANT/INJECT IT, YOU WOULD BE TOLD THAT THERE IS A DREADFUL PANDEMIC, AND AT EVERY STEP YOU WOULD BE FORCED TO TAKE IT AS A NECESSARY "VACCINATION." AND A “PCR TEST”.

BY YOUR GOVERNMENT, THE AIRLINES, THE EMPLOYER, THE WAITER AT THE RESTAURANT, THE FDA, THE EMA, THE WORLD HEALTH ORGANIZATION...

AND YET IMAGINE THAT MANY PEOPLE WOULD DIE FROM IT, AND THEY WOULD BE YOUR RELATIVES AND FRIENDS.

BUT YOU WOULD BE THE ONE WHO WOULD HAVE TO PROVE THAT IT WAS BECAUSE OF IT.

IMAGINE BEING SURROUNDED BY CENSORSHIP, BEING RIDICULED, HAVING YOUR RIGHTS TO DO YOUR JOB, MOVE AROUND, OR EVEN SPEAK THE TRUTH AT ALL TAKEN AWAY FROM YOU....

ISN’T THIS A BRIGHT FURTURE AND A FANTASTIC REALITY?

ARE YOU AGAINST SCIENCE? AGAINST PROGRESS? AGAINST PREVENTING DISEASES?



https://www.nextbigfuture.com/2015/05/pfizer-partnering-with-ido-bachelet-on.html

Pfizer is cooperating with the DNA robot laboratory managed by Prof. Ido Bachelet at Bar-Ilan University. Bachelet has developed a method of producing innovative DNA molecules with characteristics that can be used to "program" them to reach specific locations in the body and carry out pre-programmed operations there in response to stimulation from the body. This cooperation was revealed in a lecture by Pfizer president of worldwide research and development (WRD), portfolio strategy and investment committee chairman, and executive VP Mikael Dolstein at the IATI Biomed Conference in Tel Aviv being concluded today.

Research will focus on the possibility that the robots will deliver the medical proteins to designated tissue.

Bachelet came to Bar-Ilan from the Massachusetts Institute of Technology (MIT) several years ago. At a Tedmed event held two years ago, he explained, "In order to make a nanometric robot, we first of all create a selected DNA sequence, and then fold it using a process called DNA origami. With this method, a person can give a command to a computer, which folds the DNA molecule as needed.

"The result is that a DNA sequence can be made in the form of a clam, for example, and containing a drug. The DNA molecule, however, contains a code activated upon encountering certain materials in the body. For example, the clam can be designed to change its shape and release the drug only when it meets a cancer cell or the right tissue.

"In addition, the molecules can receive signals from each other, and can theoretically change their shape according to signals from the body, and can be pre-programmed to attach themselves to one another. In the future, it will be possible to combine each such molecule with a miniature antenna. When the antenna receives an external signal, it will make a small change in the molecule that will make it open or close, and dissipate or connect itself to another molecule."



In a brief talk, Bachelet said DNA nanobots will soon be tried in a critically ill leukemia patient. The patient, who has been given roughly six months to live, will receive an injection of DNA nanobots designed to interact with and destroy leukemia cells—while causing virtually zero collateral damage in healthy tissue.

According to Bachelet, his team have successfully tested their method in cell cultures and animals and written two papers on the subject, one in Science and one in Nature.

Contemporary cancer therapies involving invasive surgery and blasts of drugs can be as painful and damaging to the body as the disease itself. If Bachelet's approach proves successful in humans, and is backed by more research in the coming years, the team’s work could signal a transformational moment in cancer treatment.

If this treatment works this will be a medical breakthrough and can be used for many other diseases by delivering drugs more effectively without causing side effects.

2012 Video with answers from George Church, Ido Bachelet and Shawn Douglas on the medical DNA double helix clamshell nanobucket nanobot



George Church indicates the smart DNA nanobot has applications beyond nanomedicine. Applications where there is any need for programmable and targeted release or interaction at the cellular or near molecular scale.

2014 Geek Time Presentation from Ido Bachelet



“AND THE LAST THING I AM GOING TO SCHOW YOU IS… PANDEMIC.

SO, WE ARE REALLY CONCERNED ABOUT PANDEMICS… ESPECIALLY INFLUENZA PANDEMICS.

SO THE BEST WAY TO AVOID PANDEMICS OR TO HANDLE PANDEMICS, IS SIMPLY TO KNOW WHERE THE VIRUS IS AND NOT TO BE THERE…

IT SOUNDS STUPID, BUT IT IS ACTUALLY THE CASE…

IF YOU COULD IDENTIFY WHERE THE VIRUS IS IN REAL TIME AND YOU CAN CONTAIN THAT AREA, YOU WOULD STOP THE PANDEMIC, YOU WOULD STOP THE DISEASE… OK?


SO, WHAT WE DEVELOPED IS A SENSOR… COMPOSED OF CARBON NANOTUBES FUNCTIONALIZED WITH ALL KIND OF THINGS… THE SENSOR IS EXTREMELY SENSITIVE… WE’VE BUILT THIS APPLICATION… THEY SEND THEIR GPS COORDINATES TO OUR SERVER SO WE CAN SORT OF RECONSTRUCT A REAL MAP…

I HOPE YOU ENJOYED THIS AND UNDESTOOND WHAT BIONICS IS ALL ABOUT…

At the British Friends of Bar-Ilan University's event in Otto Uomo October 2014 Professor Ido Bachelet announced the beginning of the human treatment with nanomedicine. He indicates DNA nanobots can currently identify cells in humans with 12 different types of cancer tumors.

A human patient with late stage leukemia will be given DNA nanobot treatment. Without the DNA nanobot treatment the patient would be expected to die in the summer of 2015. Based upon animal trials they expect to remove the cancer within one month.

Within 1 or 2 years they hope to have spinal cord repair working in animals and then shortly thereafter in humans. This is working in tissue cultures.

Previously Ido Bachelet and Shawn Douglas have published work on DNA nanobots in the journal Nature and other respected science publications.

One Trillion 50 nanometer nanobots in a syringe will be injected into people to perform cellular surgery.

The DNA nanobots have been tuned to not cause an immune response.
They have been adjusted for different kinds of medical procedures. Procedures can be quick or ones that last many days.


Medicine or treatment released based upon molecular sensing - Only targeted cells are treated

Ido's daughter has a leg disease which requires frequent surgery. He is hoping his DNA nanobots will make the type of surgery she needs relatively trivial - a simple injection at a doctor's office.

We can control powerful drugs that were already developed

Effective drugs that were withdrawn from the market for excessive toxicity can be combined with DNA nanobots for effective delivery. The tiny molecular computers of the DNA nanobots can provide molecular selective control for powerful medicines that were already developed.

Using DNA origami and molecular programming, they are reality. These nanobots can seek and kill cancer cells, mimic social insect behaviors, carry out logical operators like a computer in a living animal, and they can be controlled from an Xbox. Ido Bachelet from the bio-design lab at Bar Ilan University explains this technology and how it will change medicine in the near future.

Ido Bachelet earned his Ph.D. from the Hebrew University in Jerusalem, and was a postdoctoral fellow at M.I.T. and Harvard University. He is currently an assistant professor in the Faculty of Life Sciences and the Nano-Center at Bar Ilan University, Israel, the founder of several biotech companies, and a composer of music for piano and molecules.


Researchers have injected various kinds of DNA nanobots into cockroaches. Because the nanobots are labelled with fluorescent markers, the researchers can follow them and analyse how different robot combinations affect where substances are delivered. The team says the accuracy of delivery and control of the nanobots is equivalent to a computer system.

This is the development of the vision of nanomedicine.
This is the realization of the power of DNA nanotechnology.
This is programmable dna nanotechnology.

The DNA nanotechnology cannot perform atomically precise chemistry (yet), but having control of the DNA combined with advanced synthetic biology and control of proteins and nanoparticles is clearly developing into very interesting capabilities.

"This is the first time that biological therapy has been able to match how a computer processor works," says co-author Ido Bachelet of the Institute of Nanotechnology and Advanced Materials at Bar Ilan University.

The team says it should be possible to scale up the computing power in the cockroach to that of an 8-bit computer, equivalent to a Commodore 64 or Atari 800 from the 1980s. Goni-Moreno agrees that this is feasible. "The mechanism seems easy to scale up so the complexity of the computations will soon become higher," he says.

An obvious benefit of this technology would be cancer treatments, because these must be cell-specific and current treatments are not well-targeted. But a treatment like this in mammals must overcome the immune response triggered when a foreign object enters the body.

Bachelet is confident that the team can enhance the robots' stability so that they can survive in mammals. "There is no reason why preliminary trials on humans can't start within five years," he says

Biological systems are collections of discrete molecular objects that move around and collide with each other. Cells carry out elaborate processes by precisely controlling these collisions, but developing artificial machines that can interface with and control such interactions remains a significant challenge. DNA is a natural substrate for computing and has been used to implement a diverse set of mathematical problems, logic circuits and robotics. The molecule also interfaces naturally with living systems, and different forms of DNA-based biocomputing have already been demonstrated. Here, we show that DNA origami can be used to fabricate nanoscale robots that are capable of dynamically interacting with each other in a living animal. The interactions generate logical outputs, which are relayed to switch molecular payloads on or off. As a proof of principle, we use the system to create architectures that emulate various logic gates (AND, OR, XOR, NAND, NOT, CNOT and a half adder). Following an ex vivo prototyping phase, we successfully used the DNA origami robots in living cockroaches (Blaberus discoidalis) to control a molecule that targets their cells.

Nature Nanotechnology - Universal computing by DNA origami robots in a living animal


44 pages of supplemental information

Ido Bachelet's moonshot to use nanorobotics for surgery has the potential to change lives globally. But who is the man behind the moonshot?

Ido graduated from the Hebrew University of Jerusalem with a PhD in pharmacology and experimental therapeutics. Afterwards he did two postdocs; one in engineering at MIT and one in synthetic biology in the lab of George Church at the Wyss Institute at Harvard.

Now, his group at Bar-Ilan University designs and studies diverse technologies inspired by nature.

They will deliver enzymes that break down cells via programmable nanoparticles.
Delivering insulin to tell cells to grow and regenerate tissue at the desired location.
Surgery would be performed by putting the programmable nanoparticles into saline and injecting them into the body to seek out remove bad cells and grow new cells and perform other medical work.


Research group website is here.












SOLVE FOR DISEASE X?

https://en.globes.co.il/en/article-pfizer-to-collaborate-on-bar-ilan-dna-robots-1001036703


Pfizer is cooperating with the DNA robot laboratory managed by Prof. Ido Bachelet at Bar-Ilan University. Bachelet has developed a method of producing innovative DNA molecules with characteristics that can be used to "program" them to reach specific locations in the body and carry out pre-programmed operations there in response to stimulation from the body. This cooperation was revealed in a lecture by Pfizer president of worldwide research and development (WRD), portfolio strategy and investment committee chairman, and executive VP Mikael Dolstein at the IATI Biomed Conference in Tel Aviv being concluded today.

Bar-Ilan Research & Development Co. CEO Orli Tori said, "This is Pfizer's first cooperative venture with someone in Israeli higher education. The technology is fairly new for a drug company, but Pfizer has agreed to take up the challenge and support this technology, in the hope that it will make a contribution to the company at the proper time.

"As in all of our research agreements, the company coming from the industry has the right to negotiate the acquisition of the technology at the end of the process." The financial volume of the deal was not disclosed, but most such agreements amount to several hundred thousand dollars at most. The medical sector in which cooperation will take place was also not disclosed,

but it appears that research will focus on the possibility that the robots will deliver the medical proteins to designated tissue.

Bachelet came to Bar-Ilan from the Massachusetts Institute of Technology (MIT) several years ago. At a Tedmed event held two years ago, he explained, "In order to make a nanometric robot, we first of all create a selected DNA sequence, and then fold it using a process called DNA origami. With this method, a person can give a command to a computer, which folds the DNA molecule as needed.

"The result is that a DNA sequence can be made in the form of a clam, for example, and containing a drug. The DNA molecule, however, contains a code activated upon encountering certain materials in the body. For example, the clam can be designed to change its shape and release the drug only when it meets a cancer cell or the right tissue.

"In addition, the molecules can receive signals from each other, and can theoretically change their shape according to signals from the body, and can be pre-programmed to attach themselves to one another. In the future, it will be possible to combine each such molecule with a miniature antenna.

When the antenna receives an external signal, it will make a small change in the molecule that will make it open or close, and dissipate or connect itself to another molecule."

Tori adds, "What is special about the robots is that they open and close according to signals from the surroundings, and that makes it possible to manage the disease. The robot exposes the drug to the target site according to biological signs within the body. For example were we to develop a product for diabetes, although that is not the purpose of this cooperation, it would be possible to develop a robot that would release insulin only when it sensed a rise in the blood sugar level."

Published by Globes [online], Israel business news - www.globes-online.com - on May 14, 2015

https://www.nextbigfuture.com/2015/03/ido-bachelet-dna-nanobots-summary-with.html

Disadvantages

1. Designing of nanorobot is very costly and complicated

2. Stray field might be created from electrical systems which can trigger bioelectric based molecular recognition system in biology

3. Electrical nanorobots remain vulnerable to electrical interference from other sources like radiofrequency or electric fields, electromagnetic pulse and stray fields from other in-vivo electronic devices.

4. Nanorobots are difficult to design, and customize

5. These are capable of molecular level destruction of human body thus it can cause terrible effect in terrorism field. Terrorist may make usage of nanorobots as a tool for torturing opponent community

6. Other possible threat associated with nanorobots is privacy issue.

As it dealt with designing of miniature form of devices, there are risks for snooping than that exist already.

[https://web.archive.org/web/20200718043030/https://pharmascope.org/ijrps/article/download/2523/5031]

[https://web.archive.org/web/20150911233849/http://www.nanosafe.org/home/liblocal/docs/Nanosafe%202014/Session%201/PL1%20-%20Fran%C3%A7ois%20TARDIF.pdf]

NANOROBOTS:

SOCIETAL CONCERNS: INDIVIDUAL FREEDOM, TRANSHUMANISM!!!

http://immortality-roadmap.com/nanorisk.pdf










http://jddtonline.info/index.php/jddt/article/download/891/533

There are several drawbacks with this technology like toxicity, contamination. Sometime human body generates strong immune response against them.

https://web.archive.org/web/20051218111931/http://teknologiskfremsyn.dk:80/download/58.pdf


“Nanotubes can be highly toxic”

Fifteen percent of the rats treated with carbon nanotubes suffocated to death within twenty-four hours due to clumping of the nanotubes that obstructed the bronchial passageways.








Toxicity- the issue of toxicity of nanoparticles was raised as an area in which more research is needed, particularly in terms of whether the regulatory system is sufficient.




…

And it's injected into people, soldiers, children, even infants…

Thank you Zz for this link.



Pfizer partnering with Ido Bachelet on DNA nano robots.

“No, no it’s not science fiction; it’s already happening,” said Ido Bachelet to a somewhat incredulous audience member, displaying a test tube in which he says just one drop contains approximately 1,000 billiard robots.

https://outraged.substack.com/p/pfizer-partnering-with-ido-bachelet?utm_source=cross-post&publication_id=1087020&post_id=143153580&utm_campaign=956088&isFreemail=true&r=1sq9d8&triedRedirect=true&utm_medium=email

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https://telegra.ph/Pfizer-partnering-with-Ido-Bachelet-on-DNA-nanorobots-04-03

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
For reprints, please set the canonical link back to the original Brownstone Institute Article and Author.

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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Your financial backing of Brownstone Institute goes to support writers, lawyers, scientists, economists, and other people of courage who have been professionally purged and displaced during the upheaval of our times. You can help get the truth out through their ongoing work.

https://brownstone.org/articles/the-silent-shame-of-health-institutions/

Professor Exposes the Big Lie About Cancer
By Vigilant FoxMarch 29, 2024
Cancer is “all a big money game, and it’s dollars first, patient outcome second.”

—Dr. Thomas Seyfried, Professor of Biology

“The current idea that cancer is a genetic disease is based on ideology—not on the science.”

“Our American society… doesn’t care about prevention because if they did, there would be no obesity epidemic. But there is. So that tells us the society doesn’t really care about cancer prevention.”

In Seyfried’s book, Cancer as a Metabolic Disease, he argues we should hit cancer where it hurts most by messing with its fuel supply, like using ketogenic diets to cut off the energy that cancer cells need.

It’s a way of thinking about the disease that poses bad news to the profits of the cancer treatment industry.

The above clip is from Grace Price’s Cancer: A Food-Borne Illness.

Watch the full documentary below:



https://vigilantnews.com/post/professor-exposes-the-big-lie-about-cancer/

COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher
What Mr. McKernan and his team have found contradicts the latest arguments from fact-checkers.

COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher
(CROCOTHERY/Shutterstock)
Following his discovery of DNA contamination in COVID-19 mRNA vaccines, genomic researcher Kevin McKernan has recently found that the DNA in these vaccines can potentially integrate into human DNA.

The COVID-19 vaccine spike sequence was detected in two types of chromosomes in cancer cell lines following exposure to the COVID-19 mRNA vaccine. Mr. McKernan’s findings, which he presents on his Substack blog, haven’t been peer-reviewed.
These are expected to be “rare events,” but they can happen, Mr. McKernan told The Epoch Times.
DNA Integration

Since the introduction of the COVID-19 mRNA vaccines, some members of the public have been concerned that the vaccines may modify human DNA by combining their sequences with the human genome.

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“Fact-checkers” refuted this, saying mRNA cannot be changed into DNA. Yet Mr. McKernan’s earlier work shows that DNA in the vaccine vials may be capable of changing human DNA.
Ulrike Kämmerer, a professor of human biology at the University Hospital of Würzburg in Germany, conducted earlier stages of this research.

Exposing breast and ovarian human cancer cells to Pfizer and Moderna mRNA vaccines, Ms. Kämmerer found that about half of the cells expressed the COVID-19 spike protein on their cellular surface, indicating that they had absorbed the vaccines.

Mr. McKernan then performed gene sequencing and found that these cells and their descendant cells contained vaccine DNA.

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After this, he tested to see whether any vaccine DNA combined with the cancer cell DNA, a process known as DNA integration. Integration is more of a concern in healthy cells than cancer cells because it disrupts cells’ genetic stability and integrity, increasing cancer risk.

However, because cancer cells already have unstable DNA, the effects of DNA integration are less clear.

Currently, in biomedical research, most experiments are carried out in cancer cell lines, as they are easier to obtain, experiment on, and maintain in the laboratory.

Mr. McKernan detected vaccine DNA sequences on two chromosomes in the cancer cell lines: chromosome 9 and chromosome 12. The sequencing machine detected both instances of integration twice. It is important to get two readings of the DNA integration to ensure that the integration is not a result of misreading or random error, he said.

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“The integration of ‘vaccine’ genetic information into the genome of cells was not such a surprise for me—more the confirmation of what we had to expect, unfortunately,” he told The Epoch Times.

Mr. McKernan said it is unsurprising that integration was detected on only two chromosomes with two readings of each integration. This is because integration is rare, and the genes must be sequenced many times to get more sensitive results.

The current findings are still preliminary, he said. More tests are also needed to determine whether DNA integration could be passed on to descendant cancer cells and whether this may affect cancer patients.

Also, since the test was conducted in cancer cells and not in healthy human cells, it does not suggest the same integration would occur in healthy human cells.

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However, Hiroshi Arakawa, a researcher at the Institute of Molecular Oncology who has a doctorate in molecular biology and immunology, wrote in his blog that “what happens in cultured cells can also occur in normal cells” after examining Mr. McKernan’s data.
His review of Mr. McKernan’s data also found signs of DNA integration at chromosomes 9 and 12.

“A wide variety of abnormalities can occur [in normal cells] depending on the site of genome integration,” Mr. Arakawa said.
Not Random Events

The two integration events into chromosome 9 occurred at the same place, as did the integration events into chromosome 12.

Mr. McKernan said the odds of this occurring are one in 3 billion, highlighting that where the DNA integrates may not be random.

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“There’s likely hotspots for this,” he told The Epoch Times, highlighting that in the human genome, jumping genes—short segments of DNA sequences—tend to “jump” into highly activated areas of DNA.

Highly activated DNA tends to play important roles in the human body.

The DNA integration into chromosome 12 occurred within the FAIM2 gene. Once activated, this gene creates a protein involved in programmed cell death. Since cancer cells evade cell death, the integration at chromosome 12 may be a survival-driven change.
Vaccine DNA Is Active in the Cells

Mr. McKernan said he believes that vaccine DNA is highly active in cancer cells. His sequencing machine detected the DNA of cancer cells 30 times but detected spike DNA 3,000 times.

Not only did he detect much higher levels of vaccine DNA, but he also detected new variants in certain segments of the vaccine DNA.

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These new DNA variations were not observed in unvaccinated cancer cells nor in the vaccine not exposed to the cancer cells.

Mr. McKernan said he believes that these new gene variants likely occurred because the cancer cell made copies of the vaccine DNA and created small errors.

What he and his team have found contradicts the latest arguments from fact-checkers claiming that the DNA from the mRNA vaccines cannot get into the cell, nor can it be active, he said.
DNA Contamination From mRNA Vaccine Manufacturing

DNA is present in the COVID-19 mRNA vaccines because of the manufacturing process.
This has been verified by the U.S. Food and Drug Administration (FDA), Health Canada, and the European Medicines Agency.
The mRNA vaccines are made from DNA; some of this DNA persists in the final product because of insufficient clearance.
Initially, Pfizer reported that it would use a PCR machine to produce the DNA for its mRNA vaccine. The PCR machine first makes many copies of DNA, which is then sequenced into RNA.

However, because this process wouldn’t be fast enough to meet demands, the vaccine manufacturers switched to using bacteria to mass-produce DNA as the template for the mRNA vaccine.

In this process, vaccine manufacturers introduce bacterial DNA containing the vaccine spike sequences. The bacteria make many copies of this spike DNA as they divide. This spike DNA is then harvested and transcribed into mRNA in a machine. The mRNA is then packaged into lipid nanoparticles for use in vaccination.

However, some bacterial DNA containing spike protein and other sequences could be packaged into lipid nanoparticles during the process, which would then be transported into cells during vaccination. Mr. McKernan’s earlier works have demonstrated this.
Works by molecular virologist David Speicher have shown that the amount of DNA in the mRNA vaccine vials is higher than the FDA’s allowable threshold of 10 nanograms per vaccine dose.
Mr. McKernan highlighted that compared with previous vaccines, mainly composed of naked DNA that had difficulty entering the cells, the DNA carried in the mRNA vaccines presents greater health risks, as it is packed into lipid nanoparticles and delivered straight into the cells.

https://www.theepochtimes.com/health/covid-vaccine-gene-could-integrate-into-human-cancer-cells-researcher-5604184

Subject: Fw: Dr Mike Yeadon: Introductory statement about serious crimes per Mark Sexton communication
To: [email protected] <[email protected]>
Cc: Mark Sexton

Dear Ben Bates,

I have been asked by former policeman, Mark Sexton (copied) to introduce myself to you & to indicate the fields in which I have unequivocal evidence of criminal activity.

Let me begin my outlining my credentials to have realised that the areas I will outline were incorrect in the first place.

My name is Dr Mike Yeadon. I am the most senior, former “big pharma” & biotech research executive speaking out about several serious crimes in relation to what I call the “Covid era”.

My original training was in Biochemistry & Toxicology, in which I was awarded the strongest first class joint honours degree that the School of Biomedical Sciences had ever awarded at the time (1985, University of Surrey).

Part of my undergraduate training involved research placements at the Chemical Defence Establishment, Porton Down, Wiltshire, where I was a small cog in the long term development of injected antidotes for nerve gas poisoning to protect British troops. I also worked at the then Central Laboratory of the Forensic Sciences Service, Aldermaston, Berkshire, adjacent to the Atomic Weapons Research Establishment. While with the Forensic Science Service, I received training on several precision analytical methods including mass spectrometry, then a highly technically complex method.
As far as I recall, I had security clearance for both establishments. Porton Down, then as now, is a top security facility with an international reputation.

My PhD, in the field of Pharmacology was “On the effect of opiates on respiratory function” (1988) and this was sponsored by the MOD.

After securing my PhD, which gave me a sound training in several additional subdisciplines of biology, chemistry & drug metabolism, I joined the pharmaceutical industry.

I spent 24years with “big pharma”, starting at Wellcome Research Laboratories, where I briefly worked alongside a Dr Patrick Vallance (who became Chief Scientific Advisor to the British Government).

For the longest period, I was in charge of Pfizer’s global research in the field of Allergic & Respiratory Disease Therapeutics. I left Pfizer in 2011, having reached the level of Vice President, because the company had decided to exit their large R&D base in Kent. The parting was cordial. Before leaving, I sought to find new homes for the portfolio of exploratory medicines I had helped create & was gratified that Mylan U.K. Ltd, the world’s second largest generics company, acquired much of my former portfolio soon after I had left.

I later founded & lead as CEO a highly successful biotechnology company, Ziarco Pharma Ltd. Pfizer and four other venture capital firms were investors in my company, which was acquired by Novartis Pharmaceuticals, in 2017.

My accomplishments are considered by some to have been unusual. So much so that a former Pfizer board member & previously worldwide head of R&D, Dr John LaMattina, wrote up my last venture in Forbes, a leading business magazine (February 2017).
https://www.forbes.com/sites/johnlamattina/2017/03/15/turning-pfizer-discards-into-novartis-gold-the-story-of-ziarco/

In summary, I have had a very strong training in multiple disciplines and over 30 years leadership experience in the field of inventing and testing new medicines for respiratory illnesses. I have an excellent analytical background and I can claim to be at least the equal of anyone advising the government in science.

I have no history of “conspiracy theory” or political campaigns or protests. I don’t believe I made a single public comment on anything prior to 2020.

My accomplishments in applied biomedical sciences qualify me to be taken seriously.
I ask that the evidence I marshall is evaluated thoroughly. I am confident in my assessments, which have been tested by dozens of others, internationally well known scientists and doctors.

👉 https://t.me/DrMikeYeadon

Carmen Leitch - A Tropical Fruit With a Antimicrobial Effects:

https://www.labroots.com/trending/microbiology/26800/tropical-fruit-antimicrobial-effects

#BlighiaSapida #Okpu #TropicalFruit #Antimicrobial #AntibioticResistance #Antibiotic #Disease #Pathogenicity #Medicine #PlantBiology #Microbiology #Biology

RT - Scientists discover Chernobyl ‘super worms’:

https://www.rt.com/news/593982-chernobyl-worms-radiation-study/

#OscheiusTipulae #Nematode #Extremophile #ChernobylExclusionZone #Chernobyl #Radiation #DNADamage #Genetics #Biology

Xinhua - New plant species discovered in SW China:

http://en.people.cn/n3/2024/0220/c90000-20134899.html

#LeptomischusBracteosus #Leptomischus #Rubiaceae #YunnanProvince #Botany #PlantBiology #Biology

America's COVID Response Was Based on Lies
Almost all of America's leaders have gradually pulled back their COVID mandates, requirements, and closures—even in states like California, which had imposed the most stringent and longest-lasting restrictions on the public. At the same time, the media has been gradually acknowledging the ongoing release of studies that totally refute the purported reasons behind those restrictions. This overt reversal is falsely portrayed as "learned" or "new evidence." Little acknowledgement of error is to be found. We have seen no public apology for promulgating false information, or for the vilification and delegitimization of policy experts and medical scientists like myself who spoke out correctly about data, standard knowledge about viral infections and pandemics, and fundamental biology.

The historical record is critical. We have seen a macabre Orwellian attempt to rewrite history and to blame the failure of widespread lockdowns on the lockdowns' critics, alongside absurd denials of officials' own incessant demands for them. In the Trump administration, Dr. Deborah Birx was formally in charge of the medical side of the White House's coronavirus task force during the pandemic's first year. In that capacity, she authored all written federal policy recommendations to governors and states and personally advised each state's public health officials during official visits, often with Vice President Mike Pence, who oversaw the entire task force. Upon the inauguration of President Joe Biden, Dr. Anthony Fauci became chief medical advisor and ran the Biden pandemic response.

We must acknowledge the abject failure of the Birx-Fauci policies. They were enacted, but they failed to stop the dying, failed to stop the infection from spreading, and inflicted massive damage and destruction particularly on lower-income families and on America's children.

More than 1 million American deaths have been attributed to that virus. Even after draconian measures, including school closures, stoppage of non-COVID medical care, business shutdowns, personal restrictions, and then the continuation of many restrictions and mandates in the presence of a vaccine, there was an undeniable failure—over two presidential administrations—to stop cases from rapidly escalating.

Numerous experts—including John Ioannidis, David Katz, and myself—called for targeted protection, a safer alternative to widespread lockdowns, in national media beginning in March of 2020. That proposal was rejected. History's biggest public health policy failure came at the hands of those who recommended the lockdowns and those who implemented them, not those who advised otherwise.

White House COVID task force
WASHINGTON, DC - APRIL 09: White House coronavirus response coordinator Deborah Birx speaks as (L-R) National Institute of Allergy and Infectious Diseases Director Anthony Fauci, U.S. Vice President Mike Pence and Labor Secretary Eugene Scalia... Alex Wong/Getty Images
Your daily briefing of everything you need to know

The tragic failure of reckless, unprecedented lockdowns that were contrary to established pandemic science, and the added massive harms of those policies on children, the elderly, and lower-income families, are indisputable and well-documented in numerous studies. This was the biggest, the most tragic, and the most unethical breakdown of public health leadership in modern history.

In a democracy, indeed in any ethical and free society, the truth is essential. The American people need to hear the truth—the facts, free from the political distortions, misrepresentations, and censorship. The first step is to clearly state the harsh truth in the starkest possible terms. Lies were told. Those lies harmed the public. Those lies were directly contrary to the evidence, to decades of knowledge on viral pandemics, and to long-established fundamental biology.

Here are the 10 biggest falsehoods—known for years to be false, not recently learned or proven to be so—promoted by America's public health leaders, elected and unelected officials, and now-discredited academics:

1. SARS-CoV-2 coronavirus has a far higher fatality rate than the flu by several orders of magnitude.

2. Everyone is at significant risk to die from this virus.

3. No one has any immunological protection, because this virus is completely new.

4. Asymptomatic people are major drivers of the spread.

5. Locking down—closing schools and businesses, confining people to their homes, stopping non-COVID medical care, and eliminating travel—will stop or eliminate the virus.

6. Masks will protect everyone and stop the spread.

7. The virus is known to be naturally occurring, and claiming it originated in a lab is a conspiracy theory.

8. Teachers are at especially high risk.

9. COVID vaccines stop the spread of the infection.

10. Immune protection only comes from a vaccine.

None of us are so naïve as to expect a direct apology from critics at my employer, Stanford University, or in government, academic public health, and the media. But to ensure that this never happens again, government leaders, power-driven officials, and influential academics and advisors often harboring conflicts of interest must be held accountable. Personally, I remain highly skeptical that any government investigation or commission can avoid politicization. Regardless of their intention, all such government-run inquiries will at least be perceived as politically motivated and their conclusions will be rejected outright by many. Those investigations must proceed, though, if only to seek the truth, to teach our children that truth matters, and to remember G.K. Chesterton's critical lesson that "Right is right, even if nobody does it. Wrong is wrong, even if everybody is wrong about it."

Scott W. Atlas, MD is the Robert Wesson Senior Fellow in health policy at Stanford University's Hoover Institution, Co-Director of the Global Liberty Institute, Founding Fellow of Hillsdale's Academy for Science & Freedom, and author of A Plague Upon Our House: My Fight at the Trump White House to Stop COVID from Destroying America (Bombardier Press, 2022).

The views expressed in this article are the writer's own.

Read more
How Fauci Fooled America
Untangling America from the Never-Ending COVID 'State of Emergency'
We Need a COVID Commission

https://www.newsweek.com/america-covid-response-was-based-lies-opinion-1785177


https://donshafi911.blogspot.com/2024/01/americas-covid-response-was-based-on.html

Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer?
Ivermectin, Fenbendazole, Vit C and Sodium Bicarb. But don't worry your cancer is safe because the FDA would never allow it.

Dr. Syed Haider
Cancer Treatment Options | Houston Methodist
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 the East Palestine Ohio train wreck, which may spread quite widely along the eastern seaboard, are particularly at risk of developing cancer in the coming months and years from the ingition of the vinyl chloride cargo and it’s toxic breakdown products, especially dioxins.

This post is not meant to be an exhaustive treatise on the prevention and treatment of cancer, but only to explain as simply as possible the scientific theory behind Adam Gaertner’s anti-cancer protocol, which combines 4 simple and cheap therapies that have been separately used and studied for a wide variety of human cancers with mixed results, but together have powerful synergistic effects that may, it is hoped, effectively eliminate any cancer. And at the end his simple 3 week protocol is included.

Before we begin I also have to say that I have seen many people beat end stage cancer using drastic elimination diets and a modifed Gerson juicing protocol. And of course I have known many who decided on chemotherapy, radiation and surgery. Both paths are extremely difficult and require a lot of commitment and sacrifice. Perhaps the following protocol can help more people more easily overcome cancer.

And after cancer is beaten, it pays to address the root causes because those who overcome cancer are often prone to an even more aggressive recurrence, especially if they persist in the unhealthy exposures and lifestyle habits that triggered it in the first place.

WHAT IS CANCER?

All tissues are made up of individual cellular building blocks that work together to accomplish a joint function. For example liver cells are like millions of workmen that all together make up the liver. Normally tissues maintain just the right amount of helpful worker cells. As old cells die off, new ones take their place.

Cancers arise from cells in normal tissues that start to grow uncontrollably - the old workmen don't want to die and instead find a way to become immortal. They also don't want to work anymore and begin using up resources like the nutrients and oxygen coming into the tissue via the blood. These immortal cells also multiply very quickly and if left unchecked can destroy the normal cells and then the entire organ ceases to function. Not only that but they also enter the bloodstream and travel to other distant organs and take up new residence and continue to multiply out of control.


Just as there are a tiny percentage of psychopaths and criminals in every society, who attempt to murder others and appropriate all the resources for themselves, there are cancer cells in everyone's bodies all the time that would like nothing better than to take over.

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

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And just as nations utilize a police force and military to maintain the peace, our bodies utilize specialized immune system processes and immune cells to keep the cancer cells in check - to continuously search them out and put them to death.

However, when these defenses fail due to exposure to various carcinogens or simply old age, cancerous cells can gain a foothold and destroy us.

DEFENSES AGAINST CANCER

Intracellular Cytosolic Immunity

Think of a cell like a 3D sphere. Inside the sphere there is another smaller sphere, which is the nucleus and holds the genetic material or DNA. Everything outside the nucleus is called the cytoplasm.

Steph's Nature and Science
Each individual cell has an internal immune system, called the cytosolic immune system that will monitor the cells health, and if the cell becomes cancerous will kill it in a process of cellular suicide termed apoptosis.

You can imagine this as a person's conscience.

Think of a horror movie scenario where someone becomes bitten by a mindless zombie and begins to change into a zombie themselves, feeling the first stirrings of hunger for the blood of those around them. Knowing they are doomed and wanting to preserve the lives of their loved ones they commit suicide rather than becoming a monster.

In this way our own first line of defense against cancer is a system of internal checks and balances that will lead to cellular suicide or apoptosis.

The checks and balances are a system of pro-suicide (pro-apoptotic) and anti-suicide (anti-apoptotic) pathways: p53 tumor suppressor gene, G1/S checkpoint, Hippo, TGF-β, Wnt signaling, Notch signaling, and PI3K/AKT signaling.

Within these extremely complex pathways made up of numerous interacting chemical messengers there are just a small handful of signals that can lead to cellular death: caspases, apoptosis inducing factor (AIF), endonucleases, granzymes, BH3-interacting domain death agonist (Bid), Death receptor 5 (DR5), Fas-associated protein with death domain (FADD).

A vast majority of cancers arise due to mutations affecting these critical cytosolic immunity pathways.

So the conscience of the cell, its own internal checks and balances, become distorted and do not trigger suicide as they should when the cell begins transforming into a cancer cell.

2 Zombie Stocks Coming Back from the Dead | Nasdaq
The mutations work by producing malformed proteins that do not do their usual job of triggering cellular suicide.

Usually malformed proteins would themselves be destroyed by the intracellular “chaperone” and “proteasome” systems - these are both meant to protect our cells from mutations.

The reason this does not happen in the case of most cancers is that most cancers also stimulate an internal process that makes them more resistant to the chaperone and proteasome systems - by way of the production of heat shock protein 90 (hsp90).

Ivermectin

Doctors Sue FDA For Prohibiting Use Of Ivermectin To Treat Covid
Ivermectin, the horse and cow and human drug, has traditionally been used as an antiparasitic (e.g. scabies), but also has antiviral and anti-inflammatory activities. It binds to hsp90 and other heat shock proteins blocking their ability to stabilize mutated checkpoint proteins. It likewise suppresses a number of the anti-apoptotic pathway especially TGF-β, as well as increasing the expression of p53 tumor suppressor gene pro-apoptotic pathway.

So in effect ivermectin helps the cancer cell reestablish the ability to detect that it is cancerous and thereby trigger an internal process of suicide.

Unfortunately not every cancer utilizes the pathways ivermectin targets.

And as a result of the relatively rapid replication rate of cancerous cells, and the evolutionary imperative to survive, additional mutations are often present across the tumor mass. As a result, ivermectin may be effective against only 90% of a given tumor mass; however, if the 90% is killed in this way, the remaining 10% will, by default, not be able to be corrected, leading to relapse, with the remainder becoming harder to treat - as the 10% left over multiplies and becomes the entire 100% of tumor.

Extracellular Natural Killer Cell Immunity

Immense Immunology Insight: Girl, if we were lymphocytes... You'd be a ...
Another arm of the immune system that protects against cancer is outside the cancer cell itself. We can think of this like the police force that keeps an eye out for dangerous cancer cells.

Our internal police force uses markers to identify healthy cells and unhealthy cells as well as foreign intruders like bacteria and viruses.

The markers our immune system uses for identification are called antigens - little bits of cells.

Most of our immune cells are trained to recognize foreign particles that do not belong and destroy them - like crazy immigration agent death squads.

But the Natural Killer (NK) cells are trained to check for what is supposed to be present - self-antigens - markers that indicate normal cells, kind of like ID cards.

In policing terms: NK cells wander the streets and demand everyone's papers, regardless of any evidence of a crime, and immediately execute anyone who cannot prove they belong.

"Ihre Papiere, bitte!" (Episode 48) | #FSCK 'Em All!
The rapid rate of replication of cancerous cells places them under heavy evolutionary pressure; those cells that do not express self-antigens will be targeted and destroyed by the NK cells, whereas those that do may not be - so some cancer cells develop the ability to forge their own papers and pass themselves off as normal law abiding residents, rather than dangerous alien invaders.

Those wily ones will multiply while the others die off, and eventually the entire tumor mass is comprised of cells that can trick the NK cells into leaving them alone by presenting proper identification, even though they will still be presenting other signs of being foreign - like devil horns growing out of their heads - “it’s just part of my mardi gras outfit officer”.

While this is very bad news it does open up an avenue of treatment via T cell activation.

T cell Immunity

CD 4 T cells are also called helper T cells, they aid other immune cells via the release of cytokine messengers. CD 8 T cells are also called cytotoxic T cells. Cyto for cell, toxic for toxic - i.e. they kill cancer cells.

T cells like NK cells detect self antigens and will ignore those that present them, but they also look for non self antigens (like those devil horns) as well as an additional costimulatory signal to trigger their death squad role.

It’s like they not only check your papers, but they check to make sure those horns are actually real and they make you pass a lie detector test. If they find real horns and sense signs of stress during the lie detector test they have enough evidence to declare you guilty and execute you.

Geek Comic for November 17th - You can Beat the Lie Detector Test Because…
If they just find the horns, but no signs of stress, they let you go on your way.

Cancer cells can’t avoid making weird mutated horn-like proteins, but they can figure out how to pass the lie detector test by muting their stress signals.

The way to bypass that is by subjecting them to so much stress that their ability to mute the signs of stress breaks down, and at the same time triggering more foreign proteins and stopping proliferation would also be helpful, which brings us to the other 3 therapies.

Fenbendazole, Sodium Bicarbonate & Vitamin C

Fenbendazole

Panacur Granules 22.2% [Fenbendazole] (1 lb)
Humans are not listed on the side panel
Fenbendazole is not FDA approved for use in humans, but is commonly used as an antiparasitic medication in animals, and has been studied in some human cancer studies, where it appears to be safe. It has multiple effects against cancer cells. Most significantly, it can lead to the influence the MAPK pathway to activate cellular suicide or apoptosis.

It destabilizes cellular protein structures called microtubules that are essential to cell division.

It also disrupts cancer cell energy production by blocking the breakdown of sugar (glycolysis) which is like crude oil for cells and also blocking the ability of mitochondria, the energy refining factories of cells from using the crude oil to produce the cellular equivalent of electricity, i.e. ATP - the universal bioenergy molecule.

This collection of actions may not be applicable for all cancers, however a sizable proportion are affected; as such metabolic disruption occurs which then leads to production of cellular stress signals.

An important manifestation of this is CD80, a costimulatory signal that in combination with T Cell Receptor binding to a foreign antigen, activates CD8 T-cells; alternatively if the antigen is self, it will inhibit them, as well as activate dormant NK cells in the area.

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So what’s happening here is if the cancer cell has non self antigens (those devil horns) the stress signals (failed lie detector test) will activate CD8 cytotoxic T cells to kill it.

If however the cancer cell shows a normal self antigen to the T cell along with the stress signals, the T cell will stand down but the same stress signals may still activate nearby NK cells.

Thereby some of the tumor cells will be destroyed releasing many new antigens into the area, both self and non self. These new antigens will be recognized by nearby immune cells and train them to better detect the remaining tumor cells. This triggers a far more robust immune activation and ends up in effectively nuking the area - destroying all remaining tumor as well as some friendlies and innocent bystanders mixed up in the fray.

Sodium Bicarbonate

Alkaline Diet for Cancer : Comprehensive Nutrional Guide to Cure and ...
The mechanism of sodium bicarbonate action is easy to understand, based on the Warburg effect: decreasing acidity (increasing the pH or alkalinity) outside the cancer cells impairs their ability to maintain a highly alkaline environment within themselves. That alters cancer cells' metabolism, prompting similar immune system reactions as previously discussed and igniting further cascades.

Unfortunately, if sodium bicarbonate is used without other agents from the protocol, tumors promptly become resistant and cancer-fighting benefits decrease to mere prolongation of life expectancy instead of complete elimination.

Vitamin C

Best Linus Pauling Cancer Vitamin C - Your Best Life
When ascorbic acid is used in large quantities, along with the reduced form dehydroascorbate (DHA), it induces intense oxidative stress within cancerous cells; if that stress is insufficient to destroy the cell outright, it triggers the release of numerous cytokines, including our friend CD80, which initiates the cascade described above involving CD8 cytotoxic T cells.

Not all forms of cancer are responsive to this pathway and sodium bicarbonate is capable of directly counteracting it.

As a potent immunomodulator vitamin C even has the potential to disrupt the inflammatory response involved in targeting a significant-sized tumor.

So it’s important to carefully balance the two options, and not use both simultaneously. The alkalization brought about by sodium bicarbonate won't last for particularly long; therefore, employing one after another in alternating fashion will likely provide more benefits than using just one of them at a time.

In a Nutshell

The following are four therapeutic pathways that, when used together, cause cancerous cells to undergo both apoptosis and loss of immune evasion features so the immune system can identify and attack them.

Ivermectin inhibits mutant checkpoint and cascade transduction proteins, particularly PI3K, reduces TAM anti-apoptotic signaling, and increases expression of the tumor suppressor p53 by binding to the hsp90 protein.

In addition to modulating the MAPK pathway, fenbendazole destabilizes microtubules, inhibits glycolytic metabolism, inhibits mitochondrial oxidative phosphorylation, and reduces anti-apoptotic PD-L1 expression feedback loops.

Through alkalization of the cytosolic tumor environment, sodium bicarbonate induces metabolic stress.

Vitamin C triggers oxidative stress and cytokine production.

In this method, cytosolic apoptosis signaling cascades are promoted, and effector CD8 and NK cells are infiltrated into a tumor mass through adaptive recognition of foreign antigens and inhibition of anti-apoptotic pathways in order to achieve complete remission through both self-destruct signaling pathways as well as inflammatory immune destruction of cancerous cells.

The Proposed Protocol

Unlike most traditional cytotoxic cancer therapies that destroy both cancer cells as well as regular cells and especially the body's immune system cells, this protocol stimulates the body's own innate and adaptive immune system to fight off cancer.

NLRP3 and STING enhance immune attack on cancer | Cancer Biology
This protocol should not be used in combination with most mainstream cancer treatments, such as chemotherapy or radiotherapy, due to their ability to impair the immune system that the protocol depends on.

It is likely to be most potent at the early stages of disease; further progress of the condition will prolong duration of treatment needed.

A healthy immune system takes time to ramp up the necessary response, so the protocol is based on the time required for each drug to take effect, safety data, bioavailability, and elimination time.

Day 1:

Ivermectin: 1 mg/kg by mouth

Fenbendazole: 1000mg by mouth

Sodium Bicarbonate: 1 tsp morning and evening dissolved in 1 quart of water

Day 2:

Ascorbic acid: 50 mg/kg by mouth, two doses, 8 hours apart or 20g IV, once

Day 3:

Repeat Day 1

Day 4:

Repeat Day 2

Days 5 to 10:

Fenbendazole, 200mg by mouth daily

Alternate sodium bicarbonate and ascorbic acid every other day beginning with sodium bicarb on day 5, then vitamin C on day 6, etc.

Day 11:

Ivermectin: 1 mg/kg by mouth

Fenbendazole: 1000 mg by mouth

Sodium Bicarbonate: 1 tsp morning and evening dissolved in 1 quart of water

Days 12 to 20:

Sodium Bicarbonate: 1 tsp morning and evening dissolved in 1 quart of water

Day 20:

Imaging: Check progress. Significant reduction or complete elimination of tumor mass should have occurred by this time, if not repeat the protocol.

At this time the US FDA has not approved this protocol for study or for use in humans.

It is unlikely that any pharmaceutical company will spend the millions of dollars it would take to prove this protocol in large randomized controlled trials because none of the four therapeutics are under patent and therefore cannot be effectively monetized.

Even if some billionaire decided to back this protocol, Big Pharma would move heaven and earth to prove it doesn’t work as they did with ivermectin and hydroxychloroquine for COVID.

Let me know below if you know of anyone who has utilized these 4 therapeutics together.

And finally beating cancer inside us is a great first step to healing our world, but next we need to beat the cancerous psychopaths who are destroying our societies. If not we will go the way of Rome and a new civilization will rise from our ashes.


I believe in the Judeo Christian ethic of working hard and giving back without big government. My online clinic, mygotodoc.com, exemplifies that by charging a fee that is well worth the service, but also offering free medical answers and (asynchronous) care for anyone that needs it.

The same applies at my free online Summit Long COVID Reset, exclusive weekly content, including live Q&As and much more released on my video subscription platform, and in my course, Phoenix for Healing Long Haul and Lean Vitality - all are available for a fee or for free by request.

So thank you to everyone who finds this written content valuable and supports it by being a paid subscriber (even though there are currently no paid subscriber benefits aside from a warm fuzzy feeling that you did something good). You are helping enable the significant amount of time and effort it takes to write. If you have the means also please consider donating to help support the care of those cannot afford it at mygotodoc.com/donation.

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https://blog.mygotodoc.com/p/can-2-cheap-meds-1-vitamin-and-baking

Xinhua - New gecko species discovered in China:

http://en.people.cn/n3/2024/0125/c90000-20126757.html

#GekkoKaiyai #Gekko #Kaiyai #Gecko #DabieMountains #AnhuiProvince #MitochondrialDNA #AnimalBiology #Biology

Environmental Filaments UV Light Fluorescence Darkfield Microscopy
Ana Maria Mihalcea, MD, PhD

Image: Environmental filaments collected in regular light and under UV light

I was visited by Dr. Justin Coy, a former Defense Department Contractor who has been following and validating my research. He brought me an environmental filament sample and a UV flashlight - 365nm. In this post, I am documenting the darkfield microscopy of these filaments and experiments with UV light. He was suspecting Luciferase to be present in the filaments and asked me to take a look. From my research there are metal nanoparticles in the filaments and they can cause fluorescence. Luciferase is used in in molecular biology that uses the luciferase enzyme and a substrate (such as luciferin) to study gene regulation at the level of transcription. I do not think that is the mechanism of the fluorescence of the polymers as other mechanisms using metals have been described in the literature and since Clifford Carnicoms analysis showed huge amounts of metals in the filaments that could be plausible.

There have been developments of bright orange proteins fused with Luciferase in biological systems - this remains a question for further research and discovery.

Novel NanoLuc substrates enable bright two-population bioluminescence imaging in animals

We know that embedded Quantum Dot technology can make filaments emit different light and filaments found in the blood have been shown to have bifringence. We also know that UV light can be used as an energy source by nano sensors which can embed themselves in the self assembly polymers. Karl C has done some remarkable microscopy research showing this unusual light emission which I posted here: Extraordinary Microscopy Of Self Assembly Nanotechnology - A Request For Funding Help For Karl C


Here are different images of the filaments analyzed by me observing how they change with normal light and then UV light:


Image: Darkfield Microscopy: UV light off left, UV light on right


Image above: normal light


Image: UV light

I then wanted to see if different aspects of the filament react differently to UV light, and they appear to. Some areas are more luminescent then others.


Image: UV light on, both pictures.

Below you can see a closer view of the filament under UV light, and there being very specific region that react to the UV light more:


Off the orange appearing filament a white one came forth. Magnification of 2000x on the right shows a central cavitation of the filament


Below you can see the orange environmental filament compared to a "self assembly nanotechnology hydrogel” filament from shedding in C19 unvaccinated blood with many visible Quantum Dot like structures seen embedded. The filament composition look the same except the colors differ.


Here are different areas of the filament that have enormous glow under UV light, magnification 2000x:


Here is an area of the filament with UV light:


Same without UV light:


Here are some research articles on fluorescent polymers:

New 'smart' polymer glows brighter when stretched

Spider fossils glow under UV light, a clue to their remarkable preservation

Plastics shine bright to warn of invisible cracks Damage to polymers ruptures microcapsules, releasing fluorescent molecules

I have been speaking about spider silk which is a polyamide protein and recently did microscopy on an environmental filament found:

Spider Silk Polymer Sprayed Via Geoengineering Operations From California - Darkfield Microscopy Analysis

This article explains that if metals are introduced the the nanofibers, florescence can be achieved:

Optical fluorescent spider silk electrospun nanofibers with embedded cerium oxide nanoparticles

The work demonstrates an electrospun nanocomposite of recombinant spider silk protein (rSSp) nanofibers with embedded cerium oxide (ceria) nanoparticles. RSSP (MaSp1) has been produced, extracted from goat milk, and fabricated into nanofibers using an electrospinning process. The resulting electrospun nanofibers have a mean diameter of ∼50 nm. Furthermore, ceria nanoparticles of mean diameter 10 nm were added in the spinning dope to be embedded within the generated nanofibers. These nanoparticles show certain optical activity due to optical trivaliant cerium ions, associated with formed oxygen vacancies. The formed nanocomposite shows promising mechanical properties such as the Young's modulus, elasticity (or elongation at break), and toughness. In addition, the electrospun mat becomes fluorescent with 520-nm emission upon exposure to UV light, due to excitation of the optically active ceria nanoparticles. Also, the formed nanocomposite shows a decay of its electric resistance over time upon exposure to cyclic loads at different humidity conditions. The synthesized nanocomposite can be utilized in different biomedical, textile, and sensing applications.

We do know that these polymers are used for transhumanist surveillance and synthetic biology. Here they used spider silk as an inspiration. Note how they describe that these polymers can wrap around nerves, muscles and hearts and be the next generation tissue electronic interface:

Polymer films inspired by spider silk connect biological tissues and electronic devices

Linking biological tissues with electronic devices is challenging owing to the softness of tissues and their arbitrary shapes and sizes. An innovative water-responsive, supercontractile polymer film, inspired by spider silk, allows the construction of soft, stretchable and shape-adaptive tissue–electronic interfaces.

We designed water-responsive supercontractile polymer films composed of poly(ethylene oxide) and poly(ethylene glycol)-α-cyclodextrin inclusion complex, which are initially dry, flexible and stable under ambient conditions, contract by more than 50% of their original length within seconds (about 30% per second) after wetting and become soft (about 100 kPa) and stretchable (around 600%) hydrogel thin films thereafter. This supercontraction is attributed to the aligned microporous hierarchical structures of the films, which also facilitate electronic integration. We used this film to fabricate shape-adaptive electrode arrays that simplify the implantation procedure through supercontraction and conformally wrap around nerves, muscles and hearts of different sizes when wetted for in vivo nerve stimulation and electrophysiological signal recording. This study demonstrates that this water-responsive material can play an important part in shaping the next-generation tissue–electronics interfaces as well as broadening the biomedical application of shape-adaptive materials.

Here is video of the microscopy UV light on in both videos:

UV light on playing with the focus:

I took a blood sample and applied the UV light to see what happens to the micro robots. As in my experiments with the 450nm cold laser, the robots are quite happy and seem to absorb the extra energy - if you look at the robot its light emission intensifies, and that is consistent with the WBAN article I just posted that light is an energy source for the biosensors. Energy Harvesting From The Human Body By Wireless Body Area Network - A Cause For The Electrical Conductivity Loss in Human Blood?

https://anamihalceamdphd.substack.com/p/environmental-filaments-uv-light?utm_medium=ios

THE MEDICAL FREEDOM SYMPOSIUM CONFERENCE at THE CONSCIOUS LIFE EXPO
Monday, Feb.12 - 2pm-4:30pm



FORGING THE FUTURE TERRAIN


OF WELLNESS



Join us for a riveting, powerful, inspiring exchange of motivational insights that will stir you to support and create the changes we need for our Medical Freedom!


Together We Stand!


The Supreme Court has long recognized a person's constitutionally protected liberty interest in his or her own medical autonomy, especially when those interests are secured by state laws.



Kelly Gallagher



Kelly Gallagher is an Award-winning filmmaker, writer, poet, international health activist, and wellness/survival expert. Hailing from Network TV, this 5x cancer “thriver” powered by her 6th pacemaker, and a prosthetic heart valve has successfully navigated both conventional and alternative wellness protocols for almost 40 years.


Del Bigtree



Del Bigtree inspires thousands with his unique blend of investigation, scientific expertise and solutions. As the Emmy winning producer of "The Doctors" TV series and producer of the ground-breaking documentary, Vaxxed:From Cover-up to Catastrophe, he ignited a revolution against pharmaceutical tyranny around the world. Del’s internet TV news show, The HighWire reaches out to over 100 million views. His non-profit, the Informed Consent Action Network, (ICAN), is leading worldwide investigations into drug and vaccine fraud that have already resulted in multiple winning lawsuits against US Government agencies Health and Human Services, National Institutes of Health, CDC and FDA.


Dr. Judy Mikovits



Dr. Judy Mikovits has been called one of the most accomplished scientist of her generation. Her 1991 doctoral thesis revolutionized the treatment of HIV/AIDS.. In 2020 Dr. Mikovits started Dr Solution, a company focused, not only on education, but on providing solutions for prevention and treatment of autoimmune/auto-inflammatory diseases resulting from viral infection, drugs and environmental toxins.. Her heart and passion is to focus on natural products chemistry and plant based drug and nutritional therapeutic protocols. Dr Mikovits is a New York Times Best selling author of the books Plague, Plague of Corruption, Ending Plague and the Truth about the Masks.


Dr. Mikovits is featured in both "Plandemic" films.


Dr. Jeffrey Barke



Dr. Jeffrey Barke is a board certified primary care physician in private practice for over 25 years. He has served as an Associate Clinical Professor at U.C. Irvine and a board member of the Orange County Medical Association. Dr. Barke is the author of COVID-19: A Physicians Take on the Exaggerated Fear of Corona Virus. He is a sought after speaker on the failure of government education and all things related to COVID-19. Dr. Barke is a proud founding member of America’s Frontline Doctor.He is also the co-host of the podcast: InformedDissentMedia.com

Steve Kirsch



Steve Kirsch is a Silicon Valley entrepreneur, MIT graduate and philanthropist, as well the founder of the COVID-19 Early Treatment Fund and the Vaccine Safety Research Foundation. He has been featured on 60 Minutes and profiled in Forbes. Kirsch has one of the most widely read Substacks in the world.


Dr. Byran Ardis



Dr. Bryan Ardis is a tireless researcher, seeking to weed out deception in health and medicine and provide truth through his personal research,“The Dr. Ardis” Podcast and his product formulations. In May of 2020, Dr. Ardis blew the whistle on the deadly, toxic and experimental drug, Remdesivir. Dr Ardis has been featured in many documentaries including, “Antidote” with Jason Shurka, “Watch the Water” and “Watch the Water 2”, with Stew Peters, “COVENOM-19” with Jonathan Otto, and “Propaganda Exposed” with the Bollinger’s. The Dr. Ardis Show has a mission statement which is, “Creating Doubt in Big Pharma, and Restoring Faith in Nature!” During the intentionally created supply chain issues of the fraudulent COVID pandemic, Dr. Ardis launched his own brand of all natural supplements called ArdisLabs.com. Whether by media interviews, speaking on stages, or testifying in state capital buildings, Dr. Ardis is on a mission to protect the health of innocent human beings worldwide, and help them make sense of their symptoms


Dr. Robert O. Young has been recognized as one of the top clinical scientists in the world specializing in cellular nutrition, biochemistry and microbiology. Dr. Young has devoted his life to researching the true causes of "disease," subsequently developing "The New Biology™" to help people balance their life. He is the author of over 100 published peer-reviewed articles and author and co-author of many books. The pH Miracle series of books have sold over 10 million copies and are gaining a widespread following in over 159 countries. He is best known for his four book series, The pH Miracle, The pH Miracle for Diabetes, The pH Miracle for Weight Loss and The pH Miracle for Cancer.


Last year Dr. Young and his co-author Tom Ballantyne, Jr. published 3 new books, “Truth vs Deception – Liberty vs. Tyranny - Facts vs, Fiction - Science vs, Scientism, Part 1, 2 and 3 based on the premise that if we are to remain free, we must learn the truth on what is going on around us, and not just from the media, government, etc.


While author's Dr. Robert Young and T. M. Ballantyne, Jr. (the "Truth Author," so-named by Dr. Young) will discuss the facts surrounding what Sasha Stone has called "Covidiocy," and its attendant "vaccines," along with the third book in the series, 'Let Freedom Ring', about child trafficking and its attendant evils, released in late October of 2023 (3 1/2 months ago), the underlying theme of the series is exactly what the title indicates: How to discern truth and avoid deception.


As the goal of the conference is "to create a new world based on new paradigms in various areas of life," we will address how truth liberates us from the captivity of deception."


"Given that the key to both health and happiness is right-thinking, we posit that only by recognizing and embracing actual truth can our thoughts achieve those ends. We maintain that the ultimate aim of our existence, both now and hereafter, is that we "might have joy."


Authors Young and Ballantyne


T. M. Ballantyne, Jr.



https://consciouslifeexpo.com/dr-robert-young-2024/...

PRESS CONTACT:


Dawna Shuman, Lighthouse Public Relations


[email protected]/Cell: 818-632-3297

I wonder why I'm never invited to panels?

https://www.drrobertyoung.com/post/the-medical-freedom-symposiumpost-conference-at-the-conscious-life-expo

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/

Terrifying! New LETHAL BIO-WEAPON SARS-COV-3 Built and Hid by CHINA’s ARMY | VT Foreign Policy
January 24, 2024
VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel

$ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts
Source: Embassy of Israel, Washington, D.C. and US Department of State.

by Fabio Giuseppe Carlo Carisio

VERSIONE IN ITALIANO

The news is much more alarming than the mysterious and lethal Virus with which Bill Gates and his accomplices at the World Economic Forum have continued to threaten humanity for almost a year to push all governments to accept the Pandemic Treaty of the World Health Organization (financed by Bill & Melinda Gates Foundation), the international Vaccine Passport following the example of the European Union’s Green Pass and, consequently, a new wave of mandatory vaccinations to implement the global immunization plan launched by the Microsoft’s tycoon in 1999 in the Congress Center of Rockefeller in the Villa Serbelloni in Bellagio (Como).

Perhaps it could be this new version of SARS-Cov-2, engineered in a laboratory at Being University and so powerful that it can be defined as SARS-Cov-3 due to its multiple mutations, the mysterious Disease X!

Indeed after the investigation by Gospa News (published in Italian only), the study was modified, making the most alarming parts disappear…

The suspicion comes from 4 disturbing circumstances that make the new, very dangerous Chinese research a real BIO-WEAPON capable of threatening all of humanity.

It was developed with the help of military doctors of PLA: People’s Liberation Army of China.
The laboratory experiments showed a lethality of 100% on humanized mice
The research was carried out based on previous virological tests conducted by zoologist Shi Zhengli of the Wuhan Institute of Virology
On January 21, 2024, the authors have modified the study by eliminating any terrifying reference to the 100% mortality on humanized mice, two days after the publication of the Gospa News investigation! Fortunately we have preserved both the screenshots and the original PDF study…
A first study was published on December 18, 2022 in the specialized journal Emerging Microbes & Infections and on the same date also on PubMed, the library of the National Institute for Health (NIH) of the US Department of Health, but only in the update of a few days ago the lethality of the laboratory genotype of SARS-Cov-2 called GX_P2V was made known when the new research was relaunched the first time on January 4th in pre-print by BioRxivwhere it has yet to be subjected to peer review.

The Abstract of the research up to January 21st was as brief as it was chilling:

«SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR) can cause 100% mortality in human ACE2-transgenic mice, potentially attributable to late-stage brain infection. This underscores a spillover risk of GX_P2V into humans and provides a unique model for understanding the pathogenic mechanisms of SARS-CoV-2-related viruses».


The study published on January 4th from which the role of a military doctor from the Beijing General Hospital of the PLA army can be deduced and, alongside, the study modified on January 21st with a new title and a new Abstract from which the alarm about 100% lethality in humanized mice disappeared
The updated study instead appears with a new, less alarming title “An infection and pathogenesis mouse model of SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR)” has also been sweetened in the ABSTRACT from which any reference to the VERY HIGH LETHALITY of the virus created in the laboratory DISAPPEARS:

«SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR) is highly attenuated, but can cause mortality in a specifically designed human ACE2-transgenic mouse model, making it an invaluable surrogate model for evaluating the efficacy of drugs and vaccines against SARS-CoV-2».

Even more so after this SELF-CENSORSHIP, the previous original document that we wrote about takes on importance and on which we believe it is our duty to focus even if the researchers will obviously be able to claim that they are wrong…

The study by Lai Wei et al. was conducted by Beijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Life Science and Technology, Beijing University of Chemical Technology (China), with the collaboration of State Key Laboratory of Pharmaceutical Biotechnology, Medical School, Nanjing University, but also with Research Center for Clinical Medicine, The Fifth Medical Center of PLA General Hospital, Beijing, where the military doctor Shengdong Luo, present in both studies, and his colleague Weiwei Chen work.

The latter is one of the various military hospitals that have taken the place of civilian facilities since 2016 as confirmed by a photo of the inauguration found on the internet.


One of Beijing’s civilian hospitals converted into a military facility in 2016
One of the most disturbing aspects of this research is the fact that it derives from the previous study published in 2022 which highlighted only research aimed at producing a vaccine. While this new in-depth study has in fact transformed the study into the typology products defined in the US as “Dual Use Research of Concern (DURC)”where the dual utility consists precisely in the use as a vaccine or as a bio-weapon.

From the “Smoking Gun” of Artificial SARS-Cov-2 to Beijing’s New Bio-Weapon

This new and very dangerous experiment brings us back to the studies on chimeric coronaviruses at the Wuhan Institute of Virology where the scientist Shi Zhengli infected SARS strains with HIV plasmids since 2004 thanks to the funding of the Episars project of the European Commission chaired by Romano Prodi to experiment with an artificial enhancement of the wild virus which culminated in the so-called “smoking gun” on the origin of SARS-Cov-2 of Covid 19.

«When I first saw the furin cleavage site in the viral sequence (of SARS-Cov-2 – ed.), with its arginine codons, I told my wife that it was the smoking gun for the origin of the virus”.

This is what Dr. David Baltimore, a renowned American virologist and co-discoverer of reverse transcriptase, stated in support of the thesis (now much more than a theory) of the artificial origin of the pandemic pathogen which, to summarize it in a simple way , attaches itself to human cells and becomes lethal precisely thanks to that criticality in furin.

Proof of this laboratory alteration emerged from a 2016 study, which remained almost unknown until recently, which was financed by the virologist Antony Fauci (former director of the American National Institute of Allergy and Infectious Diseases – NIAID) and conducted by US scientists, Wuhan researchers and Chinese medical doctors as revealed by the dossier of the US Senate Health Committee which not only ascertained the high probability of the artificial origin of SARS-Cov-2 but highlighted the role of American researchers…

It is now known that Fauci himself admitted before the American Congress that the theory of the virus built in the laboratory is not a conspiracy as he instead claimed in a study on natural origins published shortly after some Indian scientists from the Kusuma School of Biology in New Delhi discovered the anomalous HIV sequences and reported them in a paper published in ResearchGate.

But “they were then forced to withdraw” according to the late biologist Luc Montagnier, who was the first to publish research on artificial origin together with his biomathematician friend Jean-Claude Perez whom Gospa News interviewed exclusively a few months ago.

In our investigations of the Wuhan-Gates cycle (in homage to Bill Gates who financed the Wuhan projects through EcoHealthAliance) we highlighted how the collaboration between the US and China started on biological weapons by former presidents Bill Clinton and Jiang Zemin was fundamental to the Predict-2 project on chimeric coronavirus researches funded by the Obama-Biden administration.

This is why we have embraced the thesis of the patent expert David E. Martin who supported something very serious: according to him, in fact, the SARS-Cov-2 built between China and the US (but probably with contributions also in Canada, the United Kingdom and Ukraine) was allegedly intentionally released by the United States of America. In fact, it has brought to light too many intrigues between the research of Moderna Big Pharma (also financed by Gates and Fauci) and the Pentagon’s military agency DARPA.

So China (led by Xi Jinping disliked by the Shanghai Clan of Jiang Zemin’s political heirs and his son who strengthened the Wuhan Institute of Virology) would have suffered, for the second time after the SARS of 2003 also built in a laboratory according to Martin and Russian genomics experts, the dispersal of the virus likely occurred during the World Military Games in Wuhan in October 2019.

This is why, as reported recently by the Wall Street Journal, on the basis of documents obtained from the United States Department of Health, Chinese researchers isolated and mapped the Covid-19 virus at the end of December 2019, at least two weeks before Beijing revealed the details of the deadly virus to the world. According to the US newspaper, a Chinese researcher in Beijing uploaded an almost complete sequence of the structure of Covid into a database managed by the American government on December 28, 2019, while China shared the sequence of the virus with the World Health Organization (WHO) only 11 January 2020.

In light of these considerations, the new experimentation also conducted by Chinese military doctors takes on an even more disturbing plot. So much so as to fuel the suspicion that Beijing has built a deadly bio-weapon ready to be spread in a global bacteriological war should new Western-inspired pandemics appear.

Chinese research for a new attenuated vaccine against Covid-19

Now that we have analyzed the historical and geopolitical context, let’s briefly summarize the peculiarities of the two different studies on SARS-CoV-2 GX_P2V, the one for the 2022 vaccine and the one for the 2023 bioweapon.


The first research by Beijing University for a new anti-Covid vaccine – link at the bottom of the page
«SARS-CoV-2 related coronaviruses (SARS-CoV-2r) from Guangdong and Guangxi pangolins have been implicated in the emergence of SARS-CoV-2 and future pandemics. We previously reported the culture of a SARS-CoV-2r GX_P2V from Guangxi pangolins. Here we report the GX_P2V isolate rapidly adapted to Vero cells by acquiring two genomic mutations: an alanine to valine substitution in the nucleoprotein and a 104-nucleotide deletion in the hypervariable region (HVR) of the 3′-terminus untranslated region (3′-UTR)».

This is what we read in the Abstract on PubMed of December 2022 regarding the research by Shanshan Lu et al. entitled “Induction of significant neutralizing antibodies against SARS-CoV-2 by a highly attenuated pangolin coronavirus variant with a 104nt deletion at the 3′-UTR”.

«We further report the characterization of the GX_P2V variant (renamed GX_P2V(short_3UTR)) in in vitro and in vivo infection models. In cultured Vero, BGM and Calu-3 cells, GX_P2V(short_3UTR) had similar robust replication kinetics, and consistently produced minimum cell damage. GX_P2V(short_3UTR) infected golden hamsters and BALB/c mice but was highly attenuated. Golden hamsters infected intranasally had a short duration of productive infection in pulmonary, not extrapulmonary, tissues».

The Abstract then goes into the specifics of the development of an antidote against Covid based not on the new and controversial biotechnology of mRNA gene sera but on that of traditional vaccines:

«These productive infections induced neutralizing antibodies against pseudoviruses of GX_P2V and SARS-CoV-2. Collectively, our data show that the GX_P2V(short_3UTR) is highly attenuated in in vitro and in vivo infection models. Attenuation of the variant is likely partially due to the 104-nt deletion in the HVR in the 3′-UTR. This study furthers our understanding of pangolin coronaviruses pathogenesis and provides novel insights for the design of live attenuated vaccines against SARS-CoV-2».

The Army Laboratory Experiment for a Bacteriological Weapon

The recently published study with the already extremely alarming title “Lethal Infection of Human ACE2- Transgenic Mice Caused by SARS-CoV-2-related Pangolin Coronavirus GX_P2V(short_3UTR)” had a different impact, before it was altered on January 21 to mitigate its hazard…

This work was supported by NSFC-MFST project (China–Mongolia) (grant number 32161143027), National Key R&D Program of China (2021YFC2301804) and Biosafety Special Program (No. 19SWAQ 13).

«Two SARS-CoV-2-related pangolin coronaviruses, GD/2019 and GX/2017, were identified prior to the COVID-19 outbreak (1,2). The respective isolates, termed pCoV-GD01 and GX_P2V, were cultured in 2020 and 2017, respectively (2,3). The infectivity and pathogenicity of these isolates have been studied (4–6). The pCoV-GD01 isolate, which has higher homology with SARS-CoV-2, can infect and cause disease in both golden hamsters and hACE2 mice (4)».

We read in the pre-print research by Lai Wei et al.:

«In contrast, while GX_P2V can also infect both species, it does not appear to cause obvious disease in these animals (5,6). We previously reported that the early passaged GX_P2V isolate was actually a cell culture-adapted mutant, named GX_P2V(short_3UTR), which possesses a 104-nucleotide deletion at the 3’-UTR (6). In this study, we cloned this mutant, considering the propensity of coronaviruses to undergo rapid adaptive mutation in cell culture, and assessed its pathogenicity in hACE2 mice. We found that the GX_P2V(short_3UTR) clone can infect hACE2 mice, with high viral loads detected in both lung and brain tissues. This infection resulted in 100% mortality in the hACE2 mice. We surmise that the cause of death may be linked to the occurrence of late brain infection».


The cover of the study published on January 4 on BiorXiv before the modification on January 21, 2024 – link at the bottom of the page
Then they also recall that these SARS-CoV-2, GD/2019 and GX/2017 studies were initially carried out by the well-known scientist from the Wuhan Institute of Virology:

«To the best of our knowledge, 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. Our findings are evidently inconsistent with those of Zhengli Shiet al. (5), who tested the virulence of GX_P2V in two different hACE2 mouse models».

The discussion then becomes very technical and evidence of expert biochemists or virologists:

«It is important to note that we did not isolate the wild-type GX_P2V strain. The study by Zhengli Shi et al tested the GX_P2V(short_3UTR) variant that we reported. However, the adaptative evolutionary changes of this variant during their laboratory culture remain understudied. In fact, according to additional infection experiments, the uncloned GX_P2V(short_3UTR) also resulted in 100% mortality in hACE2 mice. Due to the propensity of coronaviruses to undergo adaptive mutation during passage culture, we cloned and analyzed mutations in GX_P2V(short_3UTR), focusing specifically on the pathogenicity of the cloned strains. The high pathogenicity mechanism of GX_P2V C7 in hACE2 mice, in the absence of the wild-type GX_P2V control, requires further investigation».

And the conclusion doesn’t suggest anything good…

«Compared to the original sequence of GX_P2V(short_3UTR), GX_P2V C7 has two amino acid mutations in the spike protein. Given the close relationship between coronavirus virulence and spike protein mutations (7), it is possible that GX_P2V C7 has undergone a virulence-enhancing mutation. However, it is important to note that our hACE2 mouse model may be relatively unique. The company has not yet published a paper on this hACE2 mouse model, but our results suggest that hACE2 may be highly expressed in the mouse brain. Additionally, according to the data provided by the company, these hACE2 mice have abnormal physiology, as indicated by relatively reduced serum triglyceride, cholesterol, and lipase levels, compared to those of wild-type C57BL/6J mice. In summary, our study provides a unique perspective on the pathogenicity of GX_P2V and offers a distinct alternative model for understanding the pathogenic mechanisms of SARS-CoV-2-related coronaviruses».

The scientific explanation is cloaked by a strong emphasis on virulence which may also appear as a “threat” on the possibility of transforming these GX_P2V genotypes into a real bacteriological weapon.

Fabio Giuseppe Carlo Carisio
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PUBMED – Induction of significant neutralizing antibodies against SARS-CoV-2 by a highly attenuated pangolin coronavirus variant with a 104nt deletion at the 3′-UTR’

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Fabio G. C. Carisio
Fabio is investigative journalist since 1991. Now geopolitics, intelligence, military, SARS-Cov-2 manmade, NWO expert and Director-founder of Gospa News: a Christian Information Journal.

His articles were published on many international media and website as SouthFront, Reseau International, Sputnik Italia, United Nation Association Westminster, Global Research, Kolozeg and more…

Most popolar investigation on VT is:

Rumsfeld Shady Heritage in Pandemic: GILEAD’s Intrigues with WHO & Wuhan Lab. Bio-Weapons’ Tests with CIA & Pentagon

Fabio Giuseppe Carlo Carisio, born on 24/2/1967 in Borgosesia, started working as a reporter when he was only 19 years old in the alpine area of Valsesia, Piedmont, his birth region in Italy. After studying literature and history at the Catholic University of the Sacred Heart in Milan, he became director of the local newspaper Notizia Oggi Vercelli and specialized in judicial reporting.

For about 15 years he is a correspondent from Northern Italy for the Italian newspapers Libero and Il Giornale, also writing important revelations on the Ustica massacre, a report on Freemasonry and organized crime.

With independent investigations, he collaborates with Carabinieri and Guardia di Finanza in important investigations that conclude with the arrest of Camorra entrepreneurs or corrupt politicians.

In July 2018 he found the counter-information web media Gospa News focused on geopolitics, terrorism, Middle East, and military intelligence.

In 2020 published the book, in Italian only, WUHAN-GATES – The New World Order Plot on SARS-Cov-2 manmade focused on the cycle of investigations Wuhan-Gates

His investigations was quoted also by The Gateway Pundit, Tasnim and others

He worked for many years for the magazine Art & Wine as an art critic and curator.

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