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More than three decades of scientific research suggests that repeatedly telling children that they are especially smart or talented leaves them vulnerable to failure, and fearful of challenges.
Children raised this way develop an implicit belief that intelligence is innate and fixed, making striving to learn seem less important than seeming smart; challenges, mistakes, and effort become threats to their ego rather than opportunities to improve.
However, teaching children to have a “growth mind-set,” which encourages effort rather than on intelligence or talent, helps make them into high achievers in school and in life. This results in “mastery-oriented” children who tend to think that intelligence is malleable and can be developed through education and hard work.
This can be done by telling stories about achievements that result from hard work. Talking about math geniuses who were born that way puts students in a fixed mind-set, but descriptions of great mathematicians who developed amazing skills over time creates a growth mind-set.
More than 80 percent of schools in America use toxic pesticides as a preventative measure, whether it‘s needed or not.
Mark Lame, an entomologist and professor at Indiana University‘s School of Public and Environmental Affairs, believes this is an entirely unnecessary practice that carries more risks than benefits to students and faculty.
The most widely used pesticides are, in fact, nerve poisons. They cause uncontrolled nerve firing, and disrupt the delicate hormone systems.
The link between pesticide exposure and health problems in children is already well established. Research has connected these endocrine-disrupting pesticides to health problems such as ADHD, autism, and infertility -- all of which are on the rise.
Professor Lame says pest problems are better managed through an integrated approach -- by preventing the conditions that attract pests into school facilities in the first place.
Lame serves as a consultant for schools around the country, helping them reduce the toxic load by implementing his Integrated Pest Management (IPM) process.
Science Daily July 21, 2007
In the January 22, 2021, lecture above, Jonathan Latham, Ph.D., discusses what he has dubbed the pandemic virus industrial complex — who they are, how they function and interact with elements within the academic, military and commercial complexes, and how they have been trying to obscure facts that indicate SARS-CoV-2 is a manmade virus that originated in a lab.
I have previously interviewed Latham a few times. He is the publisher of Independent Science News, a website that provides critical commentary on food, agriculture and biotechnology. It's part of the Bioscience Resource Project, an educational nonprofit public interest group co-founded by Latham and Allison Wilson, Ph.D., that provides independent research and analysis of genetic engineering and its risks.
Latham points out that there are currently no data to suggest a natural zoonotic origin of SARS-CoV-2. On the other hand, there's plenty of evidence and data suggesting the virus was genetically manipulated in the Wuhan Institute of Virology (WIV) in China. Much of the related research was done by a scientist called Shi Zheng-Li, Ph.D.
He goes on to summarize the Mojiang miners passage theory. This theory postulates that the virus evolved inside the bodies of six miners who became ill with a suspected novel coronavirus infection in 2012. Some of the miners were sick for several weeks — a sufficient amount of time for the virus to mutate, Latham believes.
Viral samples from the miners were sent to the WIV. Latham and Wilson believe research on these samples was what led to an accidental release of the virus in late 2019.
Latham describes the pandemic virus industrial complex as "an interlocking set of corporations and other institutions who feed off and support each other with goods and services in a self-reinforcing way." It is an enterprise that leverages public money for private profit. He also notes that many of these participants play unexpected roles. For example:
"These nontraditional roles are intended to confuse and camouflage the various moving parts of what is a complex situation," Latham says, "thereby protecting the whole from scrutiny." While there are many similarities between the military industrial complex and the pandemic virus industrial complex, there's an important difference between the two.
The pandemic virus industrial complex is public facing, and is expected to be beneficial and transparent. As such, it has an image of respectability that must be maintained, and that is why academics and philanthropic and nonprofit organizations play such important roles in this scheme.
Together, they help obscure the real agenda under a veneer of respectability and public good. In essence, they maintain the illusion that everything that's taking place is for the betterment of mankind when, in reality, it's a profit-making scheme.
Latham believes the pandemic virus industrial complex has played a decisive role in the effort to obscure the likely origin of the pandemic. He also believes this is the missing framework that helps explain the politicization of the pandemic.
In his lecture, Latham reviews some of the history of this viral pandemic industrial complex. In 2014, an Ebola outbreak in West Africa was decisively blamed on zoonotic transfer from infected bats. According to a report in EMBO Molecular Medicine,1 a 2-year-old boy playing with bats in a tree stump was Patient Zero.
However, while the paper failed to produce conclusive evidence to support its conclusion, Western media ran with this story. In West Africa, however, the rumor was that the real source of the outbreak was a hospital in Sierra Leone, which housed a biological laboratory where research on Ebola and related viruses, such as the lassa fever virus, was being done.
This research was largely funded by the U.S. Department of Defense. The reason for this funding was a recent upgrading by the U.S. Centers for Disease Control and Prevention of the lassa fever virus as a Category A infectious substance, meaning a pathogen likely to be used as a bioweapon by terrorists. The research was carried out under the auspices of the Viral Hemorrhagic Fever Consortium, led by Harvard University.
The Consortium is also tied to other academic institutions, including Tulane University, Scripps Research Institute, the University of California, San Diego, the Broad Institute of Boston and the University of Texas, as well as a number of private drug companies. According to Latham, statements made by some of the people involved in the research suggest they were taking advantage of West Africa's lax and inferior biosecurity standards.
In his book, "The Ebola Outbreak in West Africa: Corporate Gangsters, Multinationals & Rogue Politicians," Chernoh Bah provides evidence showing the Patient Zero story was a fraud. The young boy died at 18 months of age, far too young to play with bats, and he was never diagnosed with Ebola. Neither was anyone in his family. The first recorded case of Ebola was actually found in Guinea, some three months after the little boy had died.
Bah also found other gaping holes in the narrative. For example, despite widespread sampling, no Ebola virus was ever found in any animal, and no animal die-offs occurred before the outbreak, which tends to be typical in natural zoonotic spillover events. Despite the obvious problems with the official narrative, no formal investigation of the lab leak theory was ever performed.
According to Latham, we can learn a number of things from this story. First of all, lab escapes are likely more common than we think, and widely considered zoonotic outbreaks may not be zoonotic in origin at all. Another example is the AIDS epidemic, which you can learn about in the book "The River: A Journey to the Source of HIV and AIDS."
The second thing we can learn from the West African Ebola story relates to the money trail. The U.S. Department of Defense funded the research done by the Viral Hemorrhagic Fever Consortium. Other oft-used alternative sources are public health funding and international aid. Whatever the case, be it biodefense, public health funding or relief aid, the money comes from We the People.
Thirdly, corporate members of the Consortium had a specific business model in mind, and it had nothing to do with protecting vulnerable Africans from lassa or Ebola. The goal of drug companies is to sell vaccines, drugs and diagnostic tools, primarily to the U.S. or European militaries.
The fact that the 2014 Ebola outbreak narrative went unchallenged shows a disturbing lack of academic rigor, and it was certainly not the first time. As noted by Latham, scientists are failing in their role to pursue and promulgate knowledge and understanding.
"Instead, more and more frequently, academia creates fictions," he says. They create "convenient, self-serving narratives." Legacy media works hand-in-hand with such academics, acting as a megaphone for their dubious scientific claims.
One example of how businesses use academics to shape a narrative and manipulate public opinion was when, in May 2020, 77 Nobel laureates signed a public letter urging the U.S. government to reinstate funding to EcoHealth Alliance, which has subcontracted gain-of-function research on coronaviruses to the WIV. Earlier that year, then-President Trump had ordered the National Institutes of Health to cancel that funding.
The letter was organized by Sir Richard Roberts, a molecular biologist and Nobel Prize winner who also happens to be a senior executive with New England Biolabs, a manufacturer of laboratory equipment and reagents.
"Cutting funds for biotech virus research threatens their core business," Latham says. So, is Roberts really a disinterested party? Or does he have a very keen interest in keeping dangerous gain-of-function research going, risks be damned?
Back in 2016, Roberts organized a similar campaign, in which 107 Nobel laureates attacked Greenpeace for supposedly blocking the approval of GMO golden rice.
The National Press Club in Washington D.C. brought nationwide attention to the letter with a formal press conference. One of the organizers of that press event was a former Monsanto PR executive, and the website created to promote the campaign was traced to the biotech industry.
"The point here is that there's nothing spontaneous about these letters," Latham says. "They're carefully choreographed PR gambits … What is really being defended is the overlapping interests of companies like New England Biolabs and Monsanto. In this world, science and scientists are useful pawns with which to shape public opinion."
One of the latest propaganda tactics employed in an effort to shape public opinion and discourage inquisitiveness is that if you're concerned about the potential for lab leaks, you're anti-science and a racist pro-Trumper.
If you file freedom of information act (FOIA) requests with scientists, you're anti-science. If you question Dr. Anthony Fauci, you're anti-science.2,3 If you're against GMOs, you're anti-science. If you're against gain-of-function research, you're anti-science. If you're anti-nuclear energy, you're anti-science. This is a ploy and nothing else. Sadly, this propaganda is now being spewed by even the most unlikely of sources, such as Mother Jones.
June 14, 2021, Mother Jones published a hit piece on the Center for Food Safety, penned by Kiera Butler.4 In May 2021, the Center for Food Safety sued the NIH in an effort to force the agency to reveal its funding of gain-of-function research.
"Virologists say this kind of research is vital and has led to many important medical discoveries, including during the COVID-19 pandemic. But Center for Food Safety argues that gain-of-function research is too dangerous to pursue," Butler writes.
"Why would this lefty food and farms group … rail against high-level virology research? The key to the answer has to do with the Center for Food Safety's long opposition to the practice of genetic engineering. In a recent phone call, I spoke to CFS's Kimbrell, who explained what he sees as the connection.
'You genetically engineer bacteria and plants, then you genetically engineer animals, then you genetically engineer embryos — all that has happened, with some promise, but also a tremendous amount of danger and threat,' he said.
'Now, viruses are not technically an organism, but they are living biological elements. So, they fit certainly within that narrative: Just because we can do something doesn't mean we should do something.'
Kimbrell said he 'absolutely' thinks the pandemic was the result of an accidental lab release. Scientists at the Wuhan Institute of Virology, he believes, used gain-of-function to enhance a coronavirus. The virus then escaped out of the lab, spread uncontrollably, and caused the COVID-19 pandemic. Hence, in effect, gain-of-function research caused the pandemic."
Butler also discusses the Organic Consumers Association, the U.S. Right to Know, the International Center for Technology Assessment, and Children's Health Defense — all of which have raised questions and concerns about this kind of dangerous research on pathogens. According to Butler, they have no business questioning such research, and their involvement could put us all in jeopardy.
"With tens of thousands of followers on social media, anti-GMO groups have the potential to turn the tide of public opinion; hanging in the balance is science that could potentially help prevent the next pandemic," she writes.
In true propagandist fashion, Butler goes on to rebut gain-of-function concerns with commentary from EcoHealth Alliance president Peter Daszak, Ph.D., one of the most conflicted individuals you could possibly find. Indeed, his conflicts of interest have become so widely known, he was recently removed from the Lancet commission charged with investigating the origin of COVID-19 because of it.5,6
Butler also goes to great lengths trying to paint the issue in political partisan colors, and quotes Dr. Peter Hotez, another highly compromised industry-funded player who has publicly called for cyberwarfare assaults on American citizens who disagree with official COVID narratives.
In a scathing rebuttal, Center for Food Safety founder attorney Andrew Kimbrell accuses Butler of "journalistic malpractice,"7 and rightfully so, in my opinion. She clearly tries to confuse readers by stressing that "gain-of-function" is a broad definition and that much of the gain-of-function research being done is both harmless and valuable.
However, that's not the kind of research the Center for Food Safety or anyone else is concerned about. The Center for Food Safety's lawsuit specifically pertains to the manipulation of pathogens in order to make them more virulent and dangerous to humans, and she didn't interview a single mainstream scientist who has warned of the dangers associated with this practice, even though there are dozens of them.
Overall, Butler's piece reads like classic propaganda, created by the very people with something to hide. As noted by GM Watch:8
"The Gates-funded Alliance for Science was quick to promote Butler's article. They're a PR campaign based at Cornell that pushes agrichemical industry views and tries to undermine the industry's critics, particularly those critics concerned about GMOs.
As part of this effort, the Alliance for Science has been posing as an expert body on myths about the pandemic, even though they have no such myth-busting expertise. An early example of this was a piece they published by their employee Mark Lynas that branded GMWatch, among others, as conspiracy theorists for saying the virus may have accidentally leaked from a lab.
On Twitter, Mary Mangan, who sits on the Alliance's advisory board, has been carefully tracking and commenting on exactly which 'anti-GMO groups' have been calling for the lab leak hypothesis to be taken seriously …
Interestingly, a reporter told HuffPost in relation to a court case involving Monsanto that she thought Mangan had tried to 'play' her to do a hit job on one of the expert witnesses critical of the company's Roundup herbicide. Could it be that Ms Butler wasn't so resistant to being played?"
Another clear propaganda piece was published by Hotez in The Daily Beast, June 21, 2021.9 In recent weeks, Fauci's role in the pandemic has become increasingly clear, and it's far from flattering. He funded dangerous research that may in fact have resulted in a global outbreak. Now, he's trying to deflect blame by saying that personal attacks on him "represent an assault on American science," and Hotez is doing what he can to strengthen that ridiculous notion.
To do so, Hotez takes it a step further, linking attacks on Fauci to attacks not only on science but also on the very foundation of democracy. According to Hotez, "moral courage and standing up for democratic values demands that the American people throw their full support behind scientists and scientific institutions. To do otherwise is to capitulate to the forces of insurrection."10
Like Butler, Hotez spends an inordinate amount of time trying to paint concerns about dangerous research on pathogens that have the potential to kill us all as a far-right, racist, anti-science, anti-democracy issue, when it's nothing of the sort.
When dangerous science has the potential to wipe out mankind, it is cause for concern among thinking individuals of all political persuasions. It's not anti-science. It's anti-recklessness, and to prevent another disaster, those responsible must be held to account for their actions. Clearly, not all science is dangerous. Being against recklessly dangerous science does not mean you're against all science or science in general.
If we want to prevent another pandemic like this from occurring in the future, we must first determine the origin of SARS-CoV-2 and how it ended up in the population. If it can be proven that it came from a lab, then we need to identify and hold those responsible for its creation and release accountable for their actions and/or neglect and, lastly, we need to prevent a reoccurrence by banning research in which pathogens are purposely manipulated to make them more dangerous.
To get to the bottom of it all, we need to look at the pandemic virus industrial complex. We need to dissect how it functions and how its members interlink and work together to obscure the truth.
Cancer is a disease of uncontrolled growth of abnormal cells. In 1971,1 President Richard Nixon declared war on cancer with a goal to make a national commitment to find a cure. Chemotherapy has been one of the primary treatments used in cancer with the objective to destroy cancer cells.2
However, chemo is technically a poison. When administered it travels throughout your body and affects every cell, unlike radiation or surgical treatments, which target precise locations.3
Glioblastoma is a specific type of brain cancer that develops from glial cells in the brain.4 It is sometimes referred to as a grade 4 astrocytoma. The tumor is fast-growing, invasive and commonly spreads throughout the brain. According to the Glioblastoma Foundation5 it can result in death as quickly as 15 months after diagnosis.
Symptoms of a glioblastoma develop rapidly as the cells grow and fluid around the tumor increases pressure in the brain.6 Some common symptoms include severe headaches, nausea and vomiting. Depending on the location of the tumor, symptoms can include weakness or sensory changes in the face, arms or legs, neurocognitive or memory issues and difficulty with balance.
Despite decades of research, researchers have written that the survival rate for individuals with glioblastoma multiforme (GBM) has not changed in more than 40 years.7 Thomas Seyfried, who I believe is one of the best cancer biologists in the world, recently published an 80-month case report follow-up on a patient with glioblastoma,8 who has lived far longer than expected.
Writing in the journal Nutrition & Metabolism in 2007,9 Seyfried and colleagues proposed that restricting calories on a ketogenic diet is an effective alternative means of treating malignant brain cancer. The researchers used an animal model to test the theory and found the method was safe and effective.
August 16, 2014, a 26-year-old man presented at University Hospital Plymouth with symptoms of a malignant brain tumor.10 The man refused the recommended standard of care and opted instead to use ketogenic metabolic therapy (KMT). He educated himself on the implementation of the diet despite pressure from health care professionals to use their treatment.
He took medication to control the seizures and strictly followed the ketogenic diet, monitoring his glucose and ketones. It took two weeks to enter therapeutic ketosis. A second MRI in January 2015 showed no noticeable progression of the tumor. Serial MRIs every three to five months showed the tumor was growing slowly, quite unlike the natural progression of a glioblastoma.
Just over two years later, an MRI showed enough tumor growth that the patient decided to undergo a debulking surgery. Histological analysis showed an invasive astrocytic tumor. The tumor cells had a chance mutation known as IDH1, which improves the length of survival.11 After surgery, the patient continued the ketogenic diet, maintaining his glucose ketone index (GKI) near or below 2.0.12
In October 2018, an MRI showed interval progression after the patient had relaxed his strict adherence to the ketogenic diet. He returned to eating a keto diet that kept his GKI at 2 and included additional interventions such as breathing exercises, stress management and moderate physical training.
Over the following 2.5 years and seven MRIs, the tumor showed slow interval progression. As of the time of the case study writing in April 2021, the patient was “active with a good quality of life, except for occasional tonic-clonic seizures and no signs of increased intracranial pressure.”13
This case study is similar to one presented in 201814 of a 38-year-old man with a diagnosis of GBM. In addition to using a calorie-restricted ketogenic diet, this patient also underwent a subtotal tumor resection and used a modified standard of care treatment including epigallocatechin gallate, hyperbaric oxygen therapy, metformin and methylfolate.
After nine months of treatment, biomarkers and clinical symptoms indicated the tumor was regressing. At the time of the case study, 24 months after the start of therapy, the patient was in excellent health and showed evidence of significant tumor regression.15
Seyfried commented in a press release from Boston College:16
"We were surprised to discover that KMT could work synergistically with the IDH1 mutation to simultaneously target the two major metabolic pathways needed to drive the growth of GBM. Glucose drives the glycolysis pathway, while glutamine drives the glutaminolysis pathway.
No tumor, including GBM, can survive without glucose and glutamine. Our study has identified a novel mechanism by which an acquired somatic mutation acts synergistically with a low carbohydrate, high fat diet to provide long-term management of a deadly brain tumor."
The team postulated that the long-term survival of the first patient whose follow-up case study was written at 80 months after diagnosis may have been in part due to the IDH1 mutation17 and KMT, both targeting glycolysis and glutaminolysis essential for GBM growth.18
Glutamine is an amino acid that plays a role in intestinal health. Glucose and glutamine are fermentable fuels in the body. Studies19 have suggested microbial protein fermentation plays a role in generating a range of molecules that may increase inflammation and tissue permeability.
Seyfried writes that glucose and glutamine may drive breast cancer growth “through substrate level phosphorylation (SLP) in both the cytoplasm (Warburg effect) and the mitochondria (Q-effect), respectively.”20
In an interview with me, Seyfried describes how cancer cell metabolism is different from normal cell metabolism, changing from respiration to fermentation.21 If you measure oxygen consumption in tumor cells it looks like they are using oxygen to make ATP. However, the mitochondria are abnormal and what Seyfried realized was that the cells were fermenting amino acids, and in particular glutamine.
Using an animal model,22 Seyfried and colleagues demonstrated that with a calorically restricted ketogenic diet and a glutamine antagonist, they could reverse disease symptoms and improve animal survival. The strategy also appeared to reduce inflammation, swelling and hemorrhaging.
He also suggests that KMT with glutamine targeting may be an effective means of improving overall survival for women with breast cancer.23 This means targeting glucose and glutamine in the treatment of cancer all but eliminates their source of energy and starves the cells, so they can't survive.
Western medicine has been operating under the theory that cancer is a genetic disease. This rules everything from research funding and treatment to the entire cancer industry. Unfortunately, despite decades of relying on this dogma, it has not led to any significant breakthrough in treatment or prevention.
Seyfried and others have advanced the theory that cancer is primarily the result of defective energy metabolism in, and damage to, the cell's mitochondria. Genetic mutations that are detectable in cancer cells are not the primary cause of cellular overgrowth but are rather a downstream effect of defective energy metabolism.24
Research data demonstrate that cancer growth is suppressed when the nucleus from a tumor cell is transferred to the cytoplasm of normal cells with normal functioning mitochondria.25 This tells us that normal mitochondria can suppress cancer growth. Conversely, for cancer cells to proliferate, you must have dysfunctional mitochondria.
Seyfried’s research has demonstrated the growth and progression of cancer can be managed using a “whole body transition from fermentable metabolites, such as glucose and glutamine, to respiratory metabolites.”26 These are primarily ketone bodies that are formed when you follow a ketogenic diet.
In “Why Cancer Needs To Be Treated as a Metabolic Disease,” I discuss many of the pathways Seyfried notes in his interview with Dr. Peter Attia. Seyfried answers questions about the different types of mitochondrial abnormalities that are found in cancer cells and why cancer cells do not self-destruct.
Changing the view of cancer from a genetic disorder to primarily a metabolic disease has a significant impact on the approaches to preventing, treating and managing cancer.27
Seyfried’s take-home message is that as long as your mitochondrial respiration remains healthy, cancer will not develop. There are several strategies you can use to help keep your mitochondria healthy. Avoiding toxic environmental factors and implementing healthy lifestyle strategies are the primary means of protecting your mitochondria.
In fact, this is the sole focus of the metabolic mitochondrial therapy program detailed in my book “Fat for Fuel.” Topping my list of strategies to optimize mitochondrial health, which you can read more about in my book, are:
Cyclical nutritional ketosis — The divergence from our ancestral diet — this massive prevalence of processed, unnatural foods and excessive amounts of added sugars, net carbs and industrial fats — is responsible for most of the damage to your mitochondria. |
Calorie restriction — Another extremely effective strategy for reducing mitochondrial free radical production is to limit the amount of fuel you feed your body. This is a noncontroversial position as calorie restriction has consistently shown many therapeutic benefits. |
Meal timing — Meal timing is also important. Specifically, eating too late in the evening, when your body doesn't need the energy, is one of the worst things you can do to your mitochondria, as it creates a buildup of ATP that is not being used. |
Normalizing your iron level — Iron also plays an important role in mitochondrial function, and contrary to popular belief, excessive iron levels are far more prevalent than iron deficiency. Virtually all men over the age of 16 and post-menopausal women are at risk of high iron. |
Exercise — Exercise upregulates genes that promote mitochondrial efficiency, helping them grow and divide so that you have more mitochondria. By placing an increased energy demand on your cells, free radicals signal that you need more mitochondria to meet the energy demand. As a result, your body adapts to your level of activity by creating more mitochondria and making them work more efficiently. |
Nutritional supplements — The following nutrients and cofactors are also needed for mitochondrial enzymes to function properly:
|
1 Who is Dr. Robert Malone?
Dr. Robert Malone invented the mRNA and DNA vaccine core platform technology. He has grave concerns about the lack of transparency of side effects, censoring of discussion and the lack of informed consent that these bring. Learn more.
2 Instead of encouraging the open sharing of information, the media and its "fact checkers" have succeeded in using the pandemic to:
The media and its "fact checkers" have succeeded in generating fear and in controlling human behavior via the pandemic. Learn more.
3 Why are variants of the SARS-CoV-2 virus unlikely to pose a significantly differing or worse risk to people with natural immunity, compared to the original?
Variants are unlikely to pose significantly differing risk to people with natural immunity compared to the original, as resistance is primarily based on your T cells, which have been shown to recognize and attack variants that are up to 80% dissimilar. SARS-CoV-2 variants are at most 0.3% dissimilar from the original, which means T cell immunity will easily recognize and protect against them. Learn more.
4 Despite there being obvious problems with the gene-based COVID-19 "vaccines," scientists are already working on which of the following?
Scientists are moving full steam ahead to produce several additional gene-based vaccines, including the first COVID-flu mRNA vaccine, a pneumococcal-COVID mRNA booster shot for adults over 65, and mRNA seasonal influenza vaccines. Learn more.
5 The term "net zero" doesn't mean zero emissions, as rich polluters will still be able to:
Carbon offsets and the new accounting trick of 'net zero' does not mean zero emissions. It means the rich polluters will continue to pollute and also grab the land and resources of those who have not polluted — indigenous people and small farmers — for carbon offsets. Learn more.
6 The evidence is now overwhelming that SARS-CoV-2 and the COVID-19 pandemic are the result of:
The evidence is now overwhelming that SARS-CoV-2 and the COVID-19 pandemic are the result of a laboratory release. Learn more.
7 Research shows a strong correlation between the rise in celiac disease and which of the following?
There's a strong correlation between the rise in celiac disease over time and the rise in glyphosate usage on wheat, which is the primary culprit in celiac disease. Learn more.