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MASSACHUSETTS COUNTIES URGE LOCKDOWN OVER RARE MOSQUITO-BORNE ILLNESS

The HighWire with Del Bigtree | August 28, 2024

Four counties in Massachusetts have initiated a voluntary curfew to mitigate a rare mosquito-borne illness known as EEE. Officials have resorted to widespread spraying of pesticides with known harmful effects on humans. But, locals are pushing back.

September 4, 2024 Posted by | Civil Liberties, Science and Pseudo-Science, Video | , | Leave a comment

Biased? WHO-Backed Study Finds No Link Between Cellphones and Cancer

By Suzanne Burdick, Ph.D. | The Defender | September 4, 2024

A scientific review commissioned by the World Health Organization (WHO) claims it found no link between cellphone use and brain cancer. The review was available online Aug. 30 in Environmental International.

The publication — which focused largely on brain cancer but also cancer risk in general — is part of a WHO-commissioned series of scientific reviews of the possible health risks of wireless radiation.

Joel Moskowitz, Ph.D., director of the Center for Family and Community Health at the University of California, Berkeley, accused the review of being biased.

Moskowitz is a member of the International Commission on the Biological Effects of Electromagnetic Fields (ICBE-EMF), a “consortium of scientists, doctors and related professionals” who study radiofrequency-electromagnetic radiation (RF-EMF) and make recommendations for RF-EMF exposure guidelines “based on the best peer-reviewed scientific research publications.”

He has conducted and disseminated research related to wireless technology and public health since 2009.

In a post published Tuesday on his Electromagnetic Radiation Safety website, Moskowitz wrote:

“The WHO selected scientists to conduct systematic literature reviews on the biologic and health risks of wireless radiation who had demonstrated their bias through prior publications by either not finding evidence of harm or dismissing any evidence they found.”

The WHO’s review reached very different conclusions than those reached by Moskowitz and his colleagues in a 2020 review of cellphone use and cancer tumor risk.

“I believe that our 2020 review of cellphone use and tumor risk is less biased and will withstand the test of time better than the new review commissioned by the WHO,” Moskowitz wrote.

Miriam Eckenfels-Garcia, director of Children’s Health Defense’s (CHD) Electromagnetic Radiation (EMR) & Wireless program, told The Defender, “Unfortunately, we are used to the WHO getting some really important things wrong.”

She added:

“The protection of human health should always be the priority and, sadly, this does not seem to be the case here.

“The fact that the WHO handpicked scientists who are clearly biased to conduct such an important review and excluded scientific voices that reached different conclusions signals what we already know — that the WHO is as captured by big industry as our own regulatory agencies.”

WHO says cellphones don’t increase risk of brain cancer

For their review, the WHO researchers looked at 5,060 study records published between 1994 and 2022 and then narrowed them down, based on multiple criteria, to 63 studies for the final analysis.

Their goal was to assess the strength and quality of the possible link between RF-EMF exposure and neoplatistic, meaning tumorous, disease.

They concluded that RF radiation from cellphone use “likely does not increase the risk of brain cancer.”

Specifically, they said there was “moderate certainty evidence” that RF-EMF from cellphones held near the head “does not increase the risk of glioma, meningioma, acoustic neuroma, pituitary tumours, and salivary gland tumours in adults, or of paediatric brain tumours.”

The WHO authors also said RF radiation from cell towers “likely does not increase the risk of childhood cancer.”

Independent researchers say otherwise

Moskowitz and his co-authors, in their 2020 review of 46 studies, found “significant evidence linking cellular phone use to increased tumor risk, especially among cell phone users with cumulative cell phone use of 1000 or more hours in their lifetime (which corresponds to about 17 min per day over 10 years), and especially among studies that employed high quality methods.”

They recommended further studies be conducted to confirm their findings.

Moskowitz noted that the 2020 review differed in important ways from the WHO’s review. For instance, the 2020 review looked at a different kind of study than the WHO review.

“Our review examined only case-control studies of tumor risk and cellphone use as we did not consider any occupational, cohort or time-trend studies to be of sufficient quality to warrant consideration,” he said.

Also, Moskowitz and his co-authors used different criteria for weeding out studies they thought might be biased.

“Most importantly,” he added, “we employed a more conventional approach to the analysis of the cumulative call time data that examined the effects of heavy cell phone use.”

Conflicts of interest

Moskowitz noted that all of the WHO’s scientific review teams have one or more members from the International Commission on Non-Ionizing Radiation Protection (ICNIRP).

ICNIRP, which Moskowitz called a “cartel,” is a German nonprofit that issues RF radiation exposure limits “produced by its own members, their former students and close colleagues.”

The wireless industry favors the ICNIRP limits because they’re designed to protect people only from radiation levels high enough to generate heat — meaning the limits turn a blind eye to the possible health effects from radiation levels lower than those needed to heat human tissue.

Moskowitz explained why it’s problematic for ICNIRP members to conduct the WHO’s reviews:

“In 2019, investigative journalists from eight European countries published 22 articles in major news media that exposed conflicts of interest in this ‘ICNIRP cartel.’ …

“The journalists argue that the cartel promotes the ICNIRP guidelines by conducting biased reviews of the scientific literature that minimize health risks from EMF [electromagnetic field] exposure. …

“By preserving the ICNIRP exposure guidelines favored by industry, the cartel ensures that the cellular industry will continue to fund their research.”

Even though a former ICNIRP member who served as editor-in-chief of the Bioelectromagnetics Society journal accused ICNIRP of “groupthink” in 2021, the WHO continues to promote the ICNIRP’s guidelines, which are similar to those adopted by the Federal Communications Commission in the U.S., Moskowitz explained.

The ICBE-EMF in 2022 published a peer-reviewed paper refuting the “thermal-only paradigm” that insists that harmful biological effects only occur from radiation levels high enough to heat human tissue.

“The preponderance of peer-reviewed research finds non-thermal effects,” Moskowitz said.

In July, Moskowitz and other scientists with ICBE-EMF called for the retraction of an earlier WHO review because it inaccurately concluded that current international limits on RF radiation protect the public from possible non-cancer health impacts from wireless radiation, including migraines, tinnitus and sleep disturbances.

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

September 4, 2024 Posted by | Deception, Science and Pseudo-Science | | Leave a comment

Integrative Approaches For Cancer

An Interview With Pierre Kory

A Midwestern Doctor and Pierre Kory, MD, MPA | The Forgotten Side of Medicine | August 29, 2024

One of the most common requests I receive from readers is to discuss treatments for cancer. This in turn speaks to a broader issue—despite there being an immense interest in holistic cancer treatments, very few resources exist for patients looking for these options. That’s because it’s been well known for decades within the integrative medical field that the fastest way to lose your medical license is to practice unapproved cancer therapies and over the decades, countless examples have been made of doctors who did so (which sadly go far beyond even what we saw throughout COVID-19).

Note: I’ve also come across numerous cases where a distant relative learned of an alternative or complementary cancer treatment provided to their relative by a doctor, was triggered by it (due to their pre-existing political viewpoints) and then was able to get sanctions directed against the doctor. Most integrative doctors are aware of this and hence often decline to treat patients they are very close to that they know would wholeheartedly support what the doctor is doing because the doctor cannot take the risk of a hostile relative.

In turn, most of the doctors I know who utilize integrative cancer therapies (and have success in treating cancer) only offer this service to longtime patients they have a very close relationship with and explicitly request for me to not send patients to them. This is a shame, because beyond integrative cancer care being almost completely inaccessible to patients, this underground atmosphere both prevents most physicians from being able to have large enough patient volumes to clearly understand which alternative therapies actually work.

Conversely, countless alternative cancer treatments exist outside of America (e.g., in Mexico) which many American patients flock to since they have no alternative, and since these facilities have zero regulatory oversight or accountability, I frequently hear of very reckless approaches being implemented at these sites that none of my more experienced colleagues would ever consider doing (and likewise we often come across numerous critical oversights in those cases).

Note: most of the doctors I know who took up treating cancer with integrative medicine didn’t want to do it because of the risks involved and primarily started because they really cared about some of their patients and felt if they did nothing the patient would likely die. As a result, most of them are “self-taught” and frequently adopt very different approaches to treating cancer.

Since I’ve been quite young (long before I went to medical school) I’ve been fascinated by the alternative cancer therapies (especially those that were buried) and I’ve helped numerous people I knew through the process. From doing so, I gained a deep appreciation for the following:

  • Many of the conventional cancer therapies have terrible outcomes that make them very hard to justify using—especially given how costly they are. Sadly, the actual risks and benefits of the conventional cancer treatments are rarely clearly presented to patients.
  • Conversely, some of the conventional cancer treatments are helpful, and in certain cases, necessary. I’ve had patients who died because they understandably refused chemo, and likewise I’ve had certain cases where I had to do everything I could to convince a naturally-minded patient or friend to do chemo, and it ultimately saved their life (as they had aggressive cancers which were chemo-sensitive).
  • Much in the same way much of the population was fanatically committed to the COVID vaccines and the boosters despite all evidence showing each vaccination only made things worse, there is also a sizable contingent of people who will do whatever their oncologist tells them to do regardless of how clear it is that the therapy is harming them, bankrupting them and not prolonging their lifespan. Initially it was very depressing for me when I was called in to speak to someone’s friend about reconsidering their disastrous chemotherapy plan, but eventually I realized that all throughout human history people have been willing to die for their beliefs so I didn’t need to take their decision to stick to a treatment plan that ultimately gave them an agonizing death personally.
  • It is possible to dramatically reduce the adverse effects of conventional cancer therapies (e.g., with ultraviolet blood irradiation) but despite many of these approaches existing, there is no interest within the conventional field towards using them.
  • Some of the suppressed treatments for cancer are phenomenal, while others provide, at best, a marginal benefit.
  • While there are certain therapeutic principles that are relatively universal with cancer, in most cases, what each patient will respond to greatly differs. Because of this, if you use a safe but unapproved therapy that has a 50% success rate, you can easily find yourself in the position where the patient who received it still dies—at which point whoever provided the therapy can be found liable by a medical board (which does happen). Conversely, if you use an approved therapy that has a 10% success rate and a high rate of harm, there is no liability for the oncologist who prescribed it.
  • The most clinically successful integrative oncologists I know all hold the opinion that cancer is a very complex disease and anyone who claims to have a single magic bullet is either hopelessly naive or a charlatan.
  • There is often a significant emotional component to cancers. When this is managed correctly, it dramatically improves outcomes, but it is often a very difficult situation to navigate, especially because people emotionally destabilize when confronted with the fear of a slow but inevitable death.
  • In most cases, a cancer is the result of an underlying imbalance within the body (i.e., “an unhealthy terrain”). In turn, success in treating a cancer requires recognizing what is creating the unhealthy terrain and utilizing a treatment approach that also treats that. Unfortunately, quite a few different things can create an unhealthy terrain, so you again run into a situation where a one-sized fits all model for cancer simply doesn’t exist.
  • The COVID-19 turbo cancers are often quite challenging to treat.

Repurposed Drugs and Cancer

The aggressive suppression of unorthodox therapies during COVID-19, while initially successful at protecting the market for the pharmaceutical industry, eventually created a climate where enough pressure built for American doctors to find ways to provide non-standard COVID-19 therapies and organizations were established to support doctors wishing to go down this path (which were ultimately successful thanks to the incredible support of the internet).

One of the prominent COVID physician dissidents is my colleague Pierre Kory who gradually transitioned to building a telemedicine practice (Leading Edge Clinic) that focuses on treating individuals with long-COVID and COVID-19 vaccine injuries (two of the largest unmet medical needs in the country). Much of his treatment approach relies upon utilizing off-patent drugs that were previously approved for another use (e.g., ivermectin), which allows him to take advantage of the drugs being easily accessible, affordable and already generally regarded as safe.

Note: Pierre Kory considers repurposed drugs to be the achilles heel of the pharmaceutical industry since the entire business depends upon selling incredibly expensive proprietary medicines under the justification it is immensely expensive to prove they are safe and effective—whereas in contrast no money can be made off the repurposed drugs (since their patents expired) which nonetheless must stay legal since they were previously proven to be safe and approved by the FDA.

As they worked with studying and treating spike protein injuries, Drs. Paul Marik and Pierre Kory gradually realized that there was also a significant need to provide non-standard approaches for treating cancer and over the last year they’ve put together a model which has been quite beneficial for many patients and are now offering that treatment to a larger group of patients through this research study. Since it is quite rare to find a US based group publicly offering integrative cancer options to their patients, I reached out to Dr. Kory and asked him if I could interview him about his approach.

Before we go further, I want to emphasize that the approach he utilizes is different than my own, something which again speaks to both how many different paths exist to treating cancer.

Note: what follows is a slightly edited version of the conversation I (AMD) and Dr. Kory (PK) had.

AMD: Thank you for agreeing to do this, I know many of my readers will appreciate you taking time out of your busy schedule for this discussion.

PK: Thanks. Since I left the system, my eyes have been opened to how many of the things we do in medicine need to be seriously examined. Medicine has provided us with an incredible set of tools for addressing many problems which have plagued humanity, but the politics and corruption in medicine have caused us to use those tools in a way that benefits Wall Street rather than our patients and this has to change. When I started this journey, my focus was on COVID-19 and the vaccine injuries, but as time has moved forward, I’ve come to see that I have an obligation to make a safer, more affordable and hopefully more effective form of cancer care available to the public.

AMD: Before we go further, I want to show you a chart I just pulled up.

PK: Wow. I had an idea of this, but I didn’t realize it was that extreme.

AMD: Since cancer (oncology) drugs are one of the primary profit centers for the medical industry, I’ve always thought that explains why so much money is spent in protecting this monopoly.

PK: Just like COVID-19…

AMD: Anyhow, could you share with everyone what brought you to be interested in treating cancer with repurposed drugs?

PK: Well as you know, becoming a COVID dissident made me much more open to questioning medical orthodoxies, and becoming very committed to using repurposed drugs. The full story is a bit longer though.

AMD: Let’s hear it!

PK: I first started learning about cancer a little over a year ago when my friend, colleague, and mentor, Professor Paul Marik, started to talk to me about a book he had just read. For those who know me and Paul, this should be a familiar story – Paul developing a scientific insight and then I become really passionate about it in his wake.

AMD: For those who don’t know, Paul Marik MD is an incredible researcher who pioneered many approaches with transformed the practice of critical care medicine and was highly respected in his field, being one of the most published and cited critical care researchers in the world. Nonetheless, that did not protect him from being excommunicated by the medical orthodoxy once he chose to utilize alternatives to the COVID-19 treatment guidelines (which actually saved his patient’s lives). Anyways, please continue Pierre.

PK: A lot of what we’re doing now revolves around the Metabolic Theory of Cancer (MTOC), which argues that cancer is a result of disrupted metabolism within the body, and hence that much of the focus in treating cancer should be on first starving the cancer cell of glucose through a ketogenic diet and then using medicines with mechanisms of actions which interfere or block numerous processes which allow the cell to become “cancerous,” i.e. normalizing cellular metabolism throughout the body rather than trying to just kill the cancerous cells.

Although Paul did not construct the MTOC, his recognition and appreciation of both the validity and the importance of the theory may eventually have more impact than all of his prior contributions. There are several reasons for this:

•The first is that cancer rates have been increasing for a while and more recently have exploded (particularly among young people) in the wake of the mRNA campaign.

•The second is that the available therapies used to treat cancer are often toxic, largely (but not completely) ineffective at improving survival (especially in solid tumors), and immensely costly.

•The third is that cancer mortality has barely budged in decades (in fact it has increased).

AMD: It’s always incredible that medical outcomes have no effect on medical spending.

PK: True that. Anyway, Paul was immensely excited about what he was learning about cancer and it became a frequent topic of conversation. That book inspired him to begin working on a project where he reviewed almost 2,000 studies on the metabolic mechanisms of hundreds of repurposed medicines and nutraceuticals as well as other metabolic interventions to treat cancer (i.e. diet).

AMD: 2000 studies? Paul is something else.

PK: You have to have that type of dedication and information retention capability to become the top researcher in your field.

AMD: What did you think of the concept when Paul first shared it with you?

PK: At the time I already knew a little about the topic of repurposed drugs in cancer because early in Covid I had become friendly with the amazing physician and journalist Justus R. Hope (a pen name) based on his writings on ivermectin for the Desert Review and his book called “Ivermectin For The World.” More importantly, I had also read his book called Surviving Cancer, Covid-19, & DiseaseThe Repurposed Drug Revolution. It was Justus (check out his Substack) who first “schooled me” on the threat that repurposed (i.e. off patent) drugs present to Pharma, and how Pharma has systematically suppressed and attacked both off-patent drugs and inexpensive, unprofitable interventions whenever they show efficacy in treating “profitable” diseases.

AMD: Oh, I always thought you came up with that. It’s great that you’re open to admitting where you got it from rather than claiming it as your own. People often don’t do that…

PK: I cite what you’ve taught me all the time as well! Anyhow, Justus’s book on cancer was inspired by the case of a close friend of his who developed glioblastoma multiforme (a nasty brain cancer). This terrible diagnosis motivated him to search and study for therapeutic interventions and/or repurposed drugs which might help his friend. He found solid evidence for a four-drug protocol which he recommended to him. His friend then proceeded to far outlive his predicted prognosis, and although he died eventually, it was from the radiation injury to his brain that he had received initially and not from the effects of his cancer.

AMD: Three quick points I wanted to share on your anecdote.

First, there’s quite a bit of evidence linking the chickenpox vaccine to a significantly increased risk of that brain cancer (which further undermines the extremely tenuous justification for that vaccine). Additionally, a few other dangerous cancers have also been linked to specific viral vaccinations.

Second, every now and then I hear a story of someone who was injured by radiation therapy that was accidentally dosed at too high of a setting.

Third, if DMSO is administered prior to radiation therapy, it dramatically reduces its complications (while simultaneously having anticancer properties and zero toxicity). In my eyes it’s unconscionable this has not entered the standard of care for oncology and I’ve spent the last month working on a series about that substance.

PK: Wow. I’ll need to look into these—a lot of the other cancer treatment ideas you’ve given have been really helpful. Also, you sadly remind me of an older dear friend and roommate that I lived with in my 20’s who developed metastatic cervical cancer who, even then, I knew had been badly injured from radiation – essentially her bowels were fried and she lived out her days on intravenous nutrition and opiates. Sad stuff.

AMD: Until they experience it, patients really don’t appreciate the side effects of radiation therapy. One of the most common problems is that it changes the tissue in the area (e.g., creating adhesions) and those can create a lot of chronic issues for people (which are often too subtle for the doctor to recognize or believe was linked to the radiation).

PK: If we circle back to Justus’s story, after I heard about it (this was still very early in Covid), I took a close relative of mine who had recently been diagnosed with melanoma for an additional consultation with an integrative oncologist I knew. Although my friend’s melanoma was completely resected and she showed no evidence of disease (NED) on imaging, the pathologists who looked at the tumor tissue (including my friend Ryan Cole, a dermatopathologist) found it suggested a high risk of recurrence and/or metastasis.

Her “system” (standard) oncologist thus proposed she use a cancer drug (an immune checkpoint inhibitor) to prevent recurrence. This was a novel use of the drug, given that she was cancer free at the time so she wasn’t sure she wanted to use it. The reason for her hesitation was that her oncologist had rightly explained that the drug had risks of adverse effects which worried her. It also didn’t help that I was a pulmonologist who had been sent numerous patients over the years with pulmonary toxicity from this same drug (i.e. I’d seen cases of organizing pneumonia).

My relative was thus greatly concerned about the potential side effects and chose to forego her system oncologist’s recommendation. The more integrative oncologist instead started her on 11 different repurposed medicines and nutraceuticals (which I was a little shocked by at the time). Although the integrative oncologist explained the conceptual scientific framework behind the regimen quite well, I wasn’t personally familiar with the evidence base or scientific rationale for the treatment protocol my relative was placed on. That would come much later. I should note that my relative is doing well and cancer free three years later, and unlike many traditional cancer patients, has had no problems tolerating her medication regimen.

AMD: One of the things I’ve always found noteworthy in medicine is that while doctors will typically recommend patients follow their oncologists recommendations, once they or someone close to them gets cancer, physicians immediately start desperately researching the subject and reaching out to anyone they know personally who intensely studies the cancer literature.

PK: I agree. My knowledge about what could have happened to my relative definitely motivated me to go outside the box for her.

PK: Anyway, Paul started becoming obsessed with studying cancer as a metabolic disease in the winter/spring of 2023 but it was not until 6 months later that that I finally read the book that inspired Paul so much, a book titled “Tripping over the Truth: How The Metabolic Theory of Cancer Is Overturning One of Medicines Most Entrenched Paradigms” by Travis Christofferson. That book would prove to be as scientifically transformative to me as “Turtles All The Way Down” was in regards to my understanding of the (non) importance and (non) safety of childhood vaccines.

I was inspired to read the book, and after meeting with Travis and Paul to design an observational trial of using repurposed medicines and dietary interventions in cancer. We designed the study together and successfully obtained IRB approval from a rigorous IRB (we have over 200 patients enrolled already). For any interested, info on the study and enrolling into it can be found here.

AMD: It’s incredible you pulled that off. Options like that are almost never available to cancer patients.

PK: A lot of this came about because I was deeply intrigued by Travis’s knowledge base and the results of one protocol of repurposed medicines that had been studied in patients with one of the nastiest cancers, glioblastoma (which is also the one that killed Senator McCain a year after diagnosis). To put it bluntly, glioblastoma, when treated with current “standard of care” (SOC) consisting of surgery, radiation, and oral temozolomide, has a horrific but well defined and reproducible median overall survival of about 15 months and a 2 year survival between 26-28%. Furthermore, those are all very aggressive therapies which can be incredibly traumatic and harmful to the patient.

In the study that blew my mind, named METRICS, a four drug repurposed medicine protocol was used (mebendazole, metformin, doxycycline, and atorvastatin) alongside the standard of care (SOC) for that cancer. They found that the treated patients lived an average of 27 months from diagnosis and had a 2 year survival of 64% compared to the well established 28% observed with SOC (despite the patients not starting the repurposed drug protocol until a median of 6 months after diagnosis). Such a sudden improvement in one cancer’s survival rate is truly remarkable if not somewhat unprecedented.

AMD: In a recent article, I made it very clear I do not support the general use of statins as there is not evidence they meaningfully decrease one’s chance of dying and conversely they have a high rate of side effects (affecting roughly 20% of users), with many of them being severe and incapacitating. At the same time however, I try to be open minded about everything, and one of the things I’ve always been surprised is that a case can be made for using them in certain cancers.

PK: Fully agree on the statin thing.

PK: Ultimately, what I learned from Seyfried and Christofferson’s papers and books (as well as lectures and interviews by Seyfried) essentially upended the conventional understanding, I like many doctors had been trained to believe causes a cell to become cancerous.

AMD: An unhealthy terrain of the body?

PK: In a way I suppose. Seyfried is the one who ultimately and nearly singlehandedly compiled all the scientific underpinnings into a coherent MTOC (metabolic theory of cancer). He found that cancer has a “metabolic” origin (i.e. problem with energy production) and not a “genetic” one (i.e. arising from mutations in genes). This might sound boring and geeky, but I cannot overemphasize the importance and applicability of Seyfried’s work (which is the culmination of the work of a smallish group of other incredible scientists and researchers over the last 100 years).

AMD: I just want to jump in and mention that one of the diseases a dysfunctional Cell Danger Response (a metabolic state mitochondria enter where the energy production of a cell is shunted to protecting it and hence its normal functions cease—which underlies many inexplicable chronic illnesses) has been linked to, is cancer.

PK: That’s really interesting. What you introduced me to the Cell Danger Response it completely changed how we looked at vaccine injured patients because we realized the mitochondrial shut down we were observing was a normal physiologic response we had to slowly coax back to normal. I only realized recently mitochondrial dysfunction was also linked to cancer.

PK: Jumping back to Seyfried’s book, more importantly, it rightly concludes from a vast body of evidence that nearly the entire scientific and oncologic community has misunderstood the true origin of cancer (they believe it is due to cells mutating by chance and then rapidly dividing and taking over the body). The implications of the erroneous somatic mutation theory (SMT) has been devastating in that it has led to the development of a range of therapies that are indiscriminately cytotoxic (kills both cancer cells and normal, healthy cells) and minimally effective if not outright harmful in terms of quality of live vs. extension of life (the stats on chemo for most cancers are deplorable, I have an upcoming article on this in my Substack series about cancer).

AMD: Another great example of this process was the Alzheimer’s field getting hijacked by the dogma amyloid production in the brain causes the disease and that treatment of Alzheimer’s thus requires destroying that amyloid. This theory has received billions in research dollars, but failed to produce a single viable therapy (even with the FDA doing everything they could to push the newest ones onto the market), and was largely a result of a study that was proven to have fabricated its data but everyone keeps on citing. In contrast, when Alzheimer’s disease is treated as a metabolic disorder, it can be treated (and data exists clearly demonstrating this) but despite the billions we spend each year searching for a cure for the disease, that proven treatment is not acknowledged by the medical field and few doctors even know it exists.

PK: It’s literally the same exact story!

PK: On the cancer front, Seyfried’s book on the MTOC was transformative to me professionally because it now dwarfs the impact of the several other practice innovations that I have been instrumental in propagating in my career (i.e., induced hypothermia in cardiac arrest patients, point-of care ultrasound at the bedside of crashing patients in the ICU, the use of IV vitamin C in septic shock, and the utility and safety of ivermectin or other repurposed drugs in Covid).

AMD: I really wish IV vitamin C for sepsis had caught on. In my experience when it’s utilized correctly, sepsis deaths rarely occur, and the hospitals I know of that use it as a standard protocol have an extraordinary low sepsis death rate. Nonetheless, most ICU doctors, despite acknowledging it’s safe will refuse to use it (regardless of what you do) even though sespsis remains the number one cause of hospital deaths (with roughly 270,000 patients dying each year).

PK: The way vitamin C for sepsis has been treated by my profession is a punch in the gut for me and it still makes me and Paul sad whenever we think about it. To your point and experience, in the first year that Paul started employing his IV vitamin C protocol for sepsis at his hospital, independent Medicare data showed the mortality rate there dropped from a stable and consistent 22% over the years down to 6% and that was in the setting of only his ICU doing it (the hospital had other ICU’s which did not). On the subject of Paul, I’d like to quote a few things from the cancer monograph (basically a book) he created after reviewing those 1800+ studies.

In putting this document together, I have invested thousands of hours, read more than 1800 peer-reviewed papers, and consulted with dozens of doctors and experts. I want to be clear that I am not suggesting I have found a cure for cancer, nor am I the first to propose using repurposed drugs for cancer. What I hope to provide is a well-researched clearinghouse of information that picks up where traditional cancer therapies leave off. I aim to inspire providers caring for cancer patients to broaden their horizons and think creatively about readily available interventions, with science to back up their efficacy, and that could improve their patients’ outcomes. 

PK: What I value so much about Paul’s monograph is that he essentially reviewed the scientific and clinical evidence for approximately 256 repurposed medicines and over 2,000 nutraceuticals. He then ranked and ordered them according to the strength of the totality of the available evidence to support their use in terms of efficacy and safety. What he found was, that although there are claims of efficacy and safety for hundreds if not thousands of treatments, only seventeen had sufficient data which met his criteria for a “strong recommendation.” Another eight he gave a “weak” recommendation. He also categorized another twenty as having “insufficient data” to recommend, despite many claims and use by various practitioners around the globe.

At this point in my life and career, learning that the current consensus theory as to the cause of cancer is built on an inaccurate scientific understanding is unsurprising to me. I add cancer to the list of “scientific dogmas” that have been exposed as being based on faulty or corrupt science (likely due to inaccuracies and medical ignorance that became self-perpetuating). Conversely, I don’t believe poor scientific underpinnings of widespread beliefs is exclusive to any one field, so I found it very helpful that Paul was able to sort through the existing data to establish which integrative cancer therapies actually have evidence supporting them.

The fact that so many cancer patients use integrative therapies despite the evidence behind them being unclear was a key reason why Paul took on this research endeavor. To quote his monograph:

We strongly endorse an Integrative approach to the management of patients with cancer. There is much confusion amongst patients (and many health care providers) as to the characteristics of integrative oncology. The use of CAM (complementary and alternative medicine) is frequently seen in the oncology setting, with nearly half of cancer patients reporting CAM use following diagnosis and as many as 91% during active chemotherapy and radiation treatment.

Fortunately, having dug into the literature, we’ve realized that, much in the same way there was real data supporting the use of repurposed drugs and nutraceuticals for Covid, there is a lot of data for supporting the use of repurposed drugs and nutraceuticals for cancer so we are able to practice approaches supported by scientific evidence, and in some cases, extensive evidence. In many cases (because the money isn’t there) those trials aren’t as robust as is typically required for widespread recommendation (ie. the costly large placebo controlled trials) but, in Paul’s list of seventeen strongly recommended treatments, the totality of in vitroin vivo, mechanistic, safety and clinical efficacy data are beyond convincing to make informed and evidence-based decisions in practice. However, again, because the money isn’t there for these off-patent approaches, this data haven’t been promoted and the oncology field is simply unaware most of it exists (e.g., the committees who make their guidelines never take any of it into consideration).

AMD: A continually recurring theme I find when researching the Forgotten Side of Medicine is that as more money is spent on medical care (e.g., the United States is the largest spender), a stronger and stronger institutional bias exists to dismiss competing therapies which can’t be monetized. In contrast, in less affluent nations that still have advanced medical systems, many remarkable therapies with lower profit margins are regularly utilized within their medical systems—for example, after Ultraviolet Blood Irradiation was invented, it took America’s hospital system by storm in the 1940s (as it dramatically improved the success rate in treating a variety of otherwise fatal or untreatable conditions) but then was buried by the American Medical Association to protect the medical monopoly. Russia and Germany however continued to use it and in the decades since, remarkable research has emerged from these countries (particularly Russia) which would completely transform the standard of care in America, but, like many things it’s almost unknown here. How does this compare to the situation with the cancer therapies you are using?

PK: In many countries — including Israel, Germany, Switzerland, India, and other
countries in Asia — by default most oncologists are dually trained and function as integrative oncologists. This is distinct from the United States, Australia, and some European countries, where most oncologists follow the traditional orthodox approaches of what some derisively call “slash, burn, and poison,” (i.e. surgery, radiation, and chemo).

AMD: Twenty years ago, there was a great book written called “German Cancer Therapies” which illustrated how many relatively benign but highly effective natural therapies are frequently utilized within Germany’s medical system—whereas in contrast most American doctors would label those approaches as quackery and scold any patient considering utilizing them.

PK: Most doctors here don’t know that in countries where integrative oncology is utilized, rather than it being “a unfocused hodgepodge of unproven therapies” it actually involves a multidisciplinary team with caregivers committed to an integrative care model. Specifically, their major focus of care is the patient’s quality of life with an emphasis on:

•Relief of symptoms, anxiety, and pain
•Quality of sleep
•Nutrition
•Nutraceutical/herbs and repurposed drugs
•Lifestyle changes.

AMD: Before you go further, I want to point out how frustrating it is that these basic common sense approaches are not utilized within our medical system. For example, as I showed in a recent article on the critical importance of sleep, there is a lot of evidence showing poor sleep (e.g., due to night shift work) dramatically increases ones risk of cancer and doubles the rate tumors grow at.

PK: Yeah, the thing I think that’s critical to understand is that integrative oncology isn’t actually that radical. It complements conventional medicine while keeping within the boundaries of scientific rigorIntegrative medicine strives to be based on rigorous research, conducted in accordance with scientific methodologies. Integrative oncology focuses on pragmatic research; pragmatic trials test interventions in the full spectrum of everyday clinical settings, in order to maximize applicability and generalizability. Such pragmatic trials allow for a multimodal integrative approach, are individualized and with patient-centered outcomes.

AMD: I feel one of the major issues with standardized medicine is that it makes it impossible to cater care to each patient’s individual circumstances—which is a huge issue because every patient, contrary to the guidelines, is different.

AMD: On that subject, what is your advice to patients who are interested in utilizing these simple approaches to increase their chances of survival if they are stuck in a medical system that’s not open to it?

PK: The best advice I can give for patients in countries where care is being managed by “orthodox” oncologists is to consult with integrative primary care physicians and have at least one of them become part of the treatment team. However, that’s often not an option for many, which touches upon why the we felt the need to prioritize the study we are now conducting (and recruiting participants for). On one hand, we want a telemedicine service to be available to cancer patients who do not have local access to either an integrative oncologist or an integrative primary care provider. More importantly however, we believe it is critical to gather the data which shows these simple approaches work, because it’s only with that data that traditional oncologists will start to incorporate such approaches into their management of cancer. I sincerely believe almost all oncologists in practice want the best for their patients, so the trick to having them adopt integrative approaches is simply to provide them with clear-cut evidence they can understand supporting a more integrative approach to cancer, and that is what we are striving to do here.

AMD: All the background you’ve provided has been very helpful. Let’s now get into the nut and bolts of what you are doing. Since one of the major legal issues in this area is appropriately informing the patient of what you will be doing, could you share the informed consent documentation the patients receive?

PK: Below is the current consent we use in my practice. A lot of work and discussion has gone into making sure it can best support each patient in making the decision that is best for them. If anyone who reads this is considering an integrative approach to cancer (regardless of who they work with) I would highly advise taking what we put together here under consideration because it applies to many of the settings where patients receive these therapies.

Cancer presents in a complex variety of forms, and therapeutic approaches can include both conventional chemotherapy, radiation and/or surgery as well as immunotherapies, herbal, nutraceutical or other natural products as well as repurposed FDA approved drugs that may enhance one’s own response to cancer, directly cause cancer cell death or at least enhance the quality of life as a patient addresses their disease. Your provider can assist you in planning proper treatment for your unique circumstance. Our objective is to provide recommendations that are in keeping with your personal healthcare goals, desires and choices.

Notice of Specialty Status: your provider is neither an oncologist (a physician specializing in the treatment of cancer) or a primary care physician. Patients should have a primary care physician and a treating oncologist who is responsible for treating their cancer. Your provider’s care should be considered adjunctive to such care. Patients should inform their primary care physician and oncologist about the supportive care and protocols they undertake with their provider. Patients should also inform their provider of any and all treatments received elsewhere on an ongoing basis. While your provider is available for counseling regarding decisions about the use of conventional treatments for malignancy as well as these complementary approaches, any decision about the alteration or discontinuation of conventional treatment is the patient’s decision made solely at their own risk and should be done with careful consideration of the advice of the oncologist and any other treating physician(s).

Notice as to Complementary/Alternative Nature of Supportive Care: While research is continually emerging in new directions in cancer care and management, the therapies offered may not be widely accepted and perhaps controversial. There may be considerable basic science, anecdotal and clinical evidence regarding these approaches, but a therapy that has not been tested within randomized controlled clinical trials is not considered by mainstream medicine to be scientifically proven. These treatments are not approved by the Food and Drug Administration for use in treating cancer. The treatments provided by your provider in support of health and a patient’s ability to heal but may not at this time be supported by a body of evidence considered sufficiently rigorous by mainstream medical institutions to support the practice for these care approaches to patients with malignancy by academic or institutional medicine. While integrative physicians have found that many patients respond well to these therapies, and, for example, improve quality of life, individual responses vary widely. Such therapies include a variety of herbal and other products derived from nature, nutritional IVs, biologics such as peptides or cell therapies, off-label use of drugs approved for purposes other than cancer or for the patient’s specific cancer and could include other emerging therapies.

Potential Adverse Reactions: While many of these are repurposed drugs and natural products which generally have a good safety profile, they can present risks of adverse reactions, particularly in patients dealing with toxicity related to cancer or interactions with drugs used in treatment. Some of these interactions are controversial and depend on the specific disease and treatment, for example, whether antioxidants can interfere with chemotherapies. The potential for adverse events will be discussed during treatment planning.

No Guarantees: As is true of any cancer therapy but particularly the case with integrative/emerging therapies, your provider makes no claims about the effectiveness of these therapies to assist patients with any form of cancer in either achieving remission or cure, or even in the successful management of pain, quality of life or any other aspect of treating or managing malignancy. Many therapies are used to assist healing capacity by enhancing your nutritional status, immune function, sense of well-being to increase your ability to function and live in comfort.

Other Treatment Options: There could be a wide variety of potential treatments for my condition that should be discussed with all treating physicians. Depending on the type of cancer and location treatment could include surgery, chemotherapy, radiation therapy, immunotherapy, certain targeted therapies, hormone therapy, stem cell transplants, precision medicine and there could be clinical trials for which you might be eligible. Some of these treatments might be provided as part of an overall plan of care while others may be alternatives to the proposed plan that should be considered.

Insurance Non-Coverage Notice: With some narrow exceptions, these therapies are considered not medically necessary and/or considered non-covered services by private insurance companies or Medicare. It is likely that no reimbursement will be available. This may also be true of coverage for related labs The patient acknowledges and agree to be financially responsible for these therapies and laboratory tests even if a denial is issued because it is considered medically unnecessary, experimental or investigational or for any other reason.

Notice to Pregnant Women: All female patients must alert their physician if they know or suspect that they are pregnant, could become pregnant during the course of treatment or are nursing.

AMD: That’s very helpful, thank you Pierre. I’d now like to jump to the question everyone’s been asking. What results are you seeing in your patients from your approach to cancer?

PK: Well, we are certainly seeing results in some of our patients! I have to admit though, at this point, it is often difficult to parse out the relative contributions to improvement between our protocol and the standard of care they are simultaneously receiving (however that knowledge will eventually come from the data compiled in our study). That said, we do have some patients showing impressive responses that are even surprising to their “system oncologists.” However, I want to be transparent and state that we also have many patients who are not showing such responses and I don’t know why as the treatments and their mechanisms should be effective independent of cancer type. It is becoming clear to me that there are some patients whose responses leave a lot to be desired and we have not closely analyzed the data enough yet to try to understand why there are such differences in response. Certainly one reason is how advanced some patients cancer is when they present as it is always easier to treat any disease the earlier you start, but even there, we have had some surprising turn arounds in advanced cases. It’s clear we still have an immense degree to learn here—which is incredible given that the modern medical field has already been given over a century to figure cancer out.

AMD: I believe your response speaks to two very important points.

First, there are numerous completely valid models for restoring the terrain of the body so that an existing cancer disappears. The great issue is that different ones apply to different ones. In turn, the most skilled integrative oncologists I know have the perceptual capacity to recognize which one is the most likely to be applicable to their patient and to switch their treatment paradigm once it’s clear it won’t work. My central difference of opinion from you is that I believe in the MOTC, but I think it’s only the underlying cause of cancer in a subset of cancers rather than all of them.

2: One of the things that’s extremely unfair about integrative oncology is that patients typically only seek it out once conventional therapies have completely failed them and they are expected to die in the immediate future. At this point, any therapy, including integrative therapies are much less likely to work (especially if chemotherapy has destroyed their immune system), and once they fail, the death is often blamed on the integrative therapy (which again makes things so challenging for doctors wishing to help these patients). Nonetheless, you still will see dramatic recoveries from those approaches (e.g., this is how many of the buried cancer treatments of the past initially proved themselves and rose to notoriety).

PK: I fully agree with you, and it’s remarkable to me how similar this dynamic is to what saw throughout COVID-19 (e.g., the repurposed drugs could save people on the verge of death, but they were dramatically more effective if instituted at the start of the illness—often having close to a 100% success rate).

AMD: Do you have any cases you could share that are representative of the typical experiences patients have under this (ever-evolving) protocol?

PK: As I just mentioned, in some cases we are seeing really dramatic results while in others we have not, which speaks to your point about the complexity of cancer. For instance, in the 6 months since we started treating we have had a number of deaths but also surprising successes. For instance:

  1. One of our patients was diagnosed with stage four breast cancer with bone metastasis. This was her fourth diagnosis since 2009. This time around she was not interested in doing chemo or radiation. Within a month of starting our treatment, she had a repeat PET scan [a way to detecting cancer throughout the body], which was completely clear of lesions.
  2. A fairly old male patient has been diagnosed with renal cell cancer that had metastasized to the lungs and bones. He was concurrently receiving immunotherapy and about a month after beginning of our therapy, he was hospitalized for arm swelling. The hospital did the repeat whole body PET scan while he was there, which was previously scheduled for a week later. The pulmonary NP was jumping out of her seat with excitement as she compared the previous, CT images of his chest with the current images, noting multiple tumors, which were completely gone and other tumors which were significantly decreased in size. Clearly this was unusual and inspiring.
  3. A patient of my partner Scott had a significant cancer and was concurrently receiving an insanely expensive and fairly dangerous conventional treatment for it. They had a remarkable response to the combined treatment, but (likely due to their oncologist convincing them we were quacks), insisted the improvement they saw was solely due to the conventional therapy they were receiving and stopped seeing us. Given this patient’s situation, I am grateful they recovered, but this again speaks to the incredible prejudices which exist within American oncology to anything that is “different.”
  4. One of the other study sites, headed by retired breast cancer surgeon Dr. Kathleen Ruddy, treated a terminal prostate cancer patient which led to a full recovery – he even told his story at a recent FLCCC conference here (starts at 7:45), it is pretty dramatic and I wish this was the rule rather than somewhat of an exception. However, I believe the most important element to this story is that Dr. Ruddy’s successes show that the success of our (very preliminary) protocol can be replicated.

AMD: Thank you so much for all of this. Do you have any final parting words for the readers here?

PK: At this stage in my career, my main goal is leave something behind that helps the generations who will follow me. That’s a major reason why I transitioned out of the high paying intensive care jobs I previously worked and switched to a more modest lifestyle where I started the (incredibly controversial) push for creating off-patent treatment protocols for individuals with Long COVID and COVID vaccine injuries. My greatest wish at this point is that I can contribute something similar to oncology because there’s so much need there.

Ultimately, the impacts of our complementary treatment approaches can only be accurately measured or estimated via collection of immense amounts of data. We already have hundreds enrolled in our study across the multiple clinic sites, the majority of whom are also receiving “standard of care,” however there are also a minority who have exhausted standard of care and were receiving nothing when they came to us. Either way, the prognosis and survival of patients with cancer is one of the most deeply studied aspects of the disease, so we think the most impactful data we can gather will be that of 1, 2, and 5 year survival of our patients when compared to traditional estimates. I really believe we will better the historical outcomes with our approach but time (and data) will tell for sure. For that reason, if you know anyone who would be interested in participating in this study, please have them reach out to us here.

AMD: Lastly, I wanted to alert my readers to your Substack (which, despite being quite busy, I frequently read).

https://pierrekorymedicalmusings.com/

PK: Thanks for the shout-out! I would also encourage my readers to subscribe to yours (which I’ve been a longtime supporter of since I believe it’s the top newsletter on Substack).

https://www.midwesterndoctor.com/

AMD: That’s very kind of you Pierre. However, to circle back to your work, I know that you’ve already published a few articles about integrative approaches to cancer on your Substack (e.g., this one and this one). Do you have any more you plan to publish, and if so roughly when?

PK: Yes, I do. I plan on writing about the history and overall efficacy of chemotherapy in cancer as well as the overall incidence and survival of different cancers over time (especially since the mRNA vaccine campaign created a cancer catastrophe), and finally to produce a summary of our approach to treating cancer using dietary interventions and repurposed medicines (from which I will borrowing heavily from Paul’s monograph).

AMD: Thanks you again for taking the time to talk here, and more importantly for doing this entire project. I know how incredibly challenging it can to be at the forefront of a contrarian movement in medicine and how much pushback the medical system directs at prominent dissidents. I wish you the best of luck in this endeavor and I sincerely hope your study (which again can be signed up for here) is able to collect the data which can move us towards a better cancer treatment paradigm that works in harmony with the body rather than trying to fight and dominate it.

PK: My pleasure, thank you for hearing me out. As I hope your readers know, this interview only scratched the surface of the cancer story, and it is my hope in the years to come we can share many of the incredible discoveries each of us have come across in this field.

Conclusion

I hope you enjoyed this interview, please let me know your thoughts on this format in the comments. It is incredible to me how much I have been able to reach out and positive affect others with this platform (e.g., I never imagined I could put something like this together and have it be seen by hundreds of thousands of people). That is in a large part thanks to you, and I sincerely appreciate all the help you have given me to help bring the world’s attention to the Forgotten Side of Medicine—the support you are giving this publication is starting to make a lot of incredible things become possible behind the scenes.

September 3, 2024 Posted by | Science and Pseudo-Science | | Leave a comment

Rising Global Temperatures Saving Millions Of Lives, Study Finds. Cold Kills 30 Times More!

By Dr. Peter F. Mayer – Linke Zeitung – August 12, 2024  

Over the past 11,000 years of the current interglacial period, phases of prosperity and cultural flourishing are clearly linked to warmer temperatures. A reduction in deaths with rising temperatures can also be observed for the last two decades.

Fact: Cold kills nearly 30 times more people than extreme heat, 4.6 million vs. 0.155 million. Rising temperatures drive up the number of heat deaths, but not in extreme heat, but in moderate heat, as TKP recently reported and broke down. However, rising temperatures also reduce the number of deaths from cold.

Bjorn Lomborg used this data to illustrate the ratios graphically:

Chart: Björn Lomborg

Overall, this has meant saving 166,000 lives per year over the last two decades. This is according to the Lancet study by Qi Zhao (2021), which TKP has already reported on.

“Globally, 5,083,173 deaths per year were associated with sub-optimal temperatures, accounting for 9.43% of all deaths. 8.52% were cold-related and 0.91% were heat-related. There were 74 temperature-related excess deaths per 100,000 population. The mortality burden varied geographically.”

Eastern Europe had the highest heat-related excess mortality rate and sub-Saharan Africa had the highest cold-related excess mortality rate.

So we see that global warming saves lives, exactly the opposite of what politicians like Health Minister Karl Lauterbach or EU-Leyen claim and of course the mainstream media.

Full article here: https://tkp.at/2024/08/11/steigende-temperaturen-retten-leben

(Translated/summarized in the English by P. Gosselin)

September 2, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular | Leave a comment

No, Evie Magazine, Climate Change is Not Causing Anxiety

By Linnea Lueken | Climate Realism | August 19, 2024

Evie Magazine, a conservative-leaning women’s publication, recently posted an article titled “Climate Change Anxiety Is A Cause For The Decline In The Birth Rate,” in which the author claims that human-caused global warming is leading to climate anxiety which misdirects its wrath at larger families. This is mostly false. Climate change is not producing anxiety so much as false and misleading alarmist media coverage is, but it is true that blaming large families for bad weather is equally wrong.

The article begins with writer Carolyn Ferguson claiming that “last year was the hottest year on record for the world,” and that the United States is somehow warming faster than the rest of the world, and that “many are feeling the effects of global warming this year.” This is false.

The idea that any given country is heating up faster than the rest of the world has been done to death, and has been claimed for just about every single country on the planet. It should be obvious that every place on earth cannot be warming faster than the rest of the world. Scientists are selecting regions and comparing them independently over different timeframes, using different datasets and methods, whatever timeframe is most optimal to show the most warming. This makes these comparisons basically worthless.

The fact for the United States is that the record of high temperature anomalies, that is, extreme heat, has not shown an increase in those high temperature events since the best records begin in 2005. (See figure below)

According to longer term data, heatwaves in the U.S. today are less frequent and severe than they were in the 1930s, as seen below:

Likewise, as discussed in this Climate Realism post, the change in the number of days with temperatures over 95 degrees Fahrenheit has actually declined for the majority of the country. Only 10 U.S. states show an increasing trend.

Even looking at proxy data globally which give an idea of ancient temperatures do not indicate we are in a period that can be described as “the hottest on record.” Today’s temperatures according to some sources appear similar to that of the Medieval or Roman warm periods, roughly 1000 to 2500 years ago, respectively. Media claims to the contrary are just propaganda.

The majority of the abnormal warming from last year occurred in Antarctica, where temperatures remained well below freezing, but was simply “less cold” than normally occurred during certain months, particularly September. A significant portion of last year’s heat globally was boosted primarily due to the natural El Niño cycle, which is known to bump up average temperatures for much of the globe. This effect is easily traced in the temperature records.

This is not to say an average warming has not occurred over the past hundred-plus years, but it is not unprecedented nor is it alarming.

The Evie post proceeds to claim that aggression rises amid higher temperatures, writing “one of the most often overlooked corollaries is a rise in communal anger and aggression.”

The “heat makes people crazy” idea has been floated several times over the years, but even the article the Evie post links to admits that it’s likely heat is not the main factor in most of the studies that found aggression. The social sciences and psychology experiments are rifle with uncontrollable variables. Without attempting to conduct any studies, the plain fact that places like Florida and Mexico, the Bahamas, and other hot tropical locales are popular relaxation destinations seems to throw cold water on the hypothesis. Why would anyone go someplace that makes them angrier or more aggressive for vacation?

Discomfort can be aggravating, certainly, but it’s not just higher temperatures alone. Ferguson then gets to the claim that mental health professionals are “seeing more patients come in with symptoms of climate change anxiety, which is supposedly the root of many activists’ anger when it comes to large families.”

Climate Realism has written extensively about how misleading the climate anxiety diagnosis is, herehere, and here, for examples, often shifting the blame from the true culprits. Something like “climate anxiety” does exist – but it is a media-driven phenomenon because of the constant drumbeat of impending doom, not from actual lived experience of warming. Constant media coverage telling people that we are hurtling towards “global boiling,” that every weather extreme is because of you and your neighbor’s use of gasoline, including from typically conservative publications like Evie Magazine, is what is causing anxiety in people.

While Evie is right that climate activists should not turn their ire on big, traditional families, they are wrong that climate anxiety is a legitimate phenomenon.

As Ferguson correctly concludes in her piece, if someone decides not to have kids, “that’s their prerogative, but they should know this decision will likely have little impact on saving our planet.”

September 1, 2024 Posted by | Deception, Mainstream Media, Warmongering, Science and Pseudo-Science, Timeless or most popular | | Leave a comment

Glimpse into the Future of Food

By Meryl Nass | Brownstone Institute | September 1, 2024

Is your food making you sick?

Suddenly, the fact that food is making us sick, really sick, has gained a lot of attention.

When Robert F. Kennedy, Jr. announced he would suspend his presidential campaign and campaign for President Trump on August 23, both he and Trump spoke about the need to improve the food supply to regain America’s health.

The same week, Tucker Carlson interviewed the sister-brother team of Casey and Calley Means, coauthors of the #1 New York Times bestseller Good Energy: The Surprising Connection Between Metabolism and Limitless Health Their thesis, borne out by thousands of medical research studies, is that food can make us very healthy or very sick. The grocery store choices many Americans have made have led us to unprecedented levels of diabetes, obesity, and other metabolic and neurologic diseases that prematurely weaken and age us, our organs, and our arteries.

There is a whole lot wrong with our available food.

  • Chemical fertilizers have led to abusing the soil, and consequently, soils became depleted of micronutrients. Unsurprisingly, foods grown in them are now lacking those nutrients.
  • Pesticides and herbicides harm humans, as well as bugs and weeds.
  • Some experts say we need to take supplements now because we can’t get what we need from our foods anymore.
  • Subsidies for wheat, corn, and soybean exceed $5 billion annually in cash plus many other forms of support, exceeding $100 billion since 1995, resulting in vast overproduction and centralization.
  • We are practically living on overprocessed junk made of sugar, salt, wheat, and seed oils.

And that is just the start. The problem could have been predicted. Food companies grew bigger and bigger, until they achieved virtual monopolies. In order to compete, they had to use the cheapest ingredients. When the few companies left standing banded together, we got industry capture of the agencies that regulated their businesses, turning regulation on its head.

Consolidation in the Meat Industry

Then the regulators issued rules that advantaged the big guys, and disadvantaged the small guys. But it was the small guys who were producing the highest quality food, in most cases. Most of them had to sell out and find something else to do. It simply became uneconomic to be a farmer.

The farmers and ranchers that were left often became the equivalent of serfs on their own land.

Did you know:

  • “Ninety-seven percent of the chicken Americans eat is produced by a farmer under contract with a big chicken company. These chicken farmers are the last independent link in an otherwise completely vertically integrated, company-owned supply chain.”
  • “Corporate consolidation is at the root of many of the structural ills of our food system. When corporations have the ability to dictate terms to farmers, farmers lose. Corporations place the burden of financial liability on farmers, dictate details of far.”
  • “Corporations also consolidate ownership of the other steps of the supply chain that farmers depend on — inputs, processing, distribution, and marketing — leaving farmers few options but to deal with an entity against which they have effectively no voice or bargaining power.”

When profitability alone, whether assisted by policy or not, determines which companies succeed and which fail, cutting corners is a necessity for American businesses — unless you have a niche food business, or are able to sell directly to consumers. This simple fact inevitably led to a race to the bottom for quality.

Look at the world’s ten largest food companies. Their sales are enormous, but should we really be consuming their products?

Perhaps the regulators could have avoided the debasement of the food supply. But they didn’t.

And now it has become a truism that Americans have the worst diet in the world.

Could food shortages be looming?

If it seems like the US, blessed with abundant natural resources, could never suffer a food shortage, think again. Did you know that while the US is the world’s largest food exporter, in 2023 the US imported more food than we exported?

Cows are under attack, allegedly because their belching methane contributes to climate change. Holland has said it must get rid of 30-50% of its cows. Ireland and Canada are also preparing to reduce the number of their cows, using the same justification.

In the US, the number of cows being raised has gradually lessened, so that now we have the same number of cows that were being raised in 1951 — but the population has increased by 125% since then. We have more than double the people, but the same number of cows. What!? Much of our beef comes from Brazil.

Pigs and chickens are now mostly raised indoors. Their industries are already consolidated to the max. But cows and other ungulates graze for most of their life, and so the beef industry has been unable to be consolidated in the same way.

But consolidation is happening instead in the slaughterhouses because you cannot process beef without a USDA inspector in a USDA-approved facility — and the number of these facilities has been dropping, as have the number of cows they can handle. Four companies now process over 80% of US beef. And that is how the ranchers are being squeezed.

Meanwhile, efforts are afoot to reduce available farmland for both planting crops and grazing animals. Bill Gates is now the #1 owner of US farmland, much of which lies fallow. Solar farms are covering land that used to grow crops — a practice recently outlawed in Italy. Plans are afoot to impose new restrictions on how land that is under conservation easements can be used.

Brave New Food

That isn’t all. The World Economic Forum, along with many governments and multinational agencies, wants to redesign our food supply. So-called plant-based meats, lab-grown meats, “synbio” products, insect protein, and other totally new foods are to replace much of the real meat people enjoy — potentially leading to even greater consolidation of food production. This would allow “rewilding” of grazing areas, allowing them to return to their natural state and, it is claimed, this would be kinder to the planet. But would it?

Much of the land used for grazing is unsuitable for growing crops or for other purposes. The manure of the animals grazing on it replenishes soil nutrients and contributes to the soil microbiome and plant growth. “Rewilding” may in fact lead to the loss of what topsoil is there and desertification of many grazing areas.

Of course, transitioning the food supply to mostly foods coming from factories is a crazy idea, because how can you make a major change in what people eat and expect it to be good for them? What micronutrients are you missing? What will the new chemicals, or newly designed proteins, or even computer-designed DNA (that will inevitably be present in these novel foods) do to us over time? What will companies be feeding the insects they farm, when food production is governed by ever cheaper inputs?

It gets worse. Real food production, by gardeners and small farmers or homesteaders, is decentralized. It cannot be controlled. Until the last 150 years, almost everyone fed themselves from food they caught, gathered, or grew.

But if food comes mainly from factories, access can be cut off. Supply chains can break down. You can be priced out of buying it. Or it could make you sick, and it might take years or generations before the source of the problem is identified. How long has it taken us to figure out that overprocessed foods are a slow poison?

There are some very big problems brewing in the food realm. Whether we like it or not, powerful forces are moving us into the Great Reset, threatening our diet in new ways, ways that most of us never dreamed of.

Identifying the Problems and Solutions

But we can get on top of what is happening, learn what we need to, and we can resist. That’s why Door to Freedom and Children’s Health Defense have unpacked all of these problems and identified possible solutions.

During a jam-packed two-day online symposium, you will learn about all facets of the attack on food, and how to resist. This is an entirely free event, with a fantastic lineup of speakers and topics. Grab a pad and pencil, because you will definitely want to take notes!

The Attack on Food and Farmers, and How to Fight Back premieres on September 6 and 7. It will remain on our channels for later viewing and sharing as well. By the end of Day 2, you will know what actions to take, both in your own backyard, and in the halls of your legislatures to create a healthier, tastier, safer, and more secure food supply.

See below for a summary and for the complete program.

September 1, 2024 Posted by | Economics, Malthusian Ideology, Phony Scarcity, Science and Pseudo-Science | , , | Leave a comment

Most Variation in All-Cause Mortality Explained by Mass COVID-19 Vaccination

Australian Ecological Analysis Points to Vaccine Campaign Causing Rising Death Counts

By Peter A. McCullough, MD, MPH | Courageous Discourse | September 1, 2024

After a pandemic, all cause mortality should go down due to a culling effect of the frail and vulnerable. We saw acute COVID-19 become the proximate cause of death in many seniors who were in the final year of natural life.

Now an analysis from Allen indicates that all-cause mortality is up in heavily vaccinated Australia and that at least two thirds in the variation per region is explained by mass COVID-19 vaccination. There are numerous well-documented fatal vaccine serious adverse events which are piling up months and years after the shots. Cumulative toxicity is another factor as a single person is not vaccinated just with the primary series (first two injections), but continued dosing every six months.

Allen, DE. 2024. The correlation between Australian Excess Deaths by State and Booster Vaccinations. Medical Research Archives, [online] 12(7).https://doi.org/10.18103/mra.v1 2i7.5485

These data call for a direct data merge of the vaccine administration and death data in Australia to explore these very uncomfortable relationships. Because the Australian government pushed the vaccines so hard, officials have been stonewalling the public on this important next analysis.

September 1, 2024 Posted by | Science and Pseudo-Science, War Crimes | , | Leave a comment

DOJ lawyer admits FDA war against ivermectin was an abuse of authority, after doctors sue government and win

Project Veritas | August 27, 2024

The attorney from the Department of Justice who defended the Food & Drug Administration in court admitted on undercover camera that the agency’s actions were an abuse of authority by the government during its public campaign against ivermectin to treat COVID-19.

A trio of doctors recently won a major legal victory in a multi-year lawsuit sparked by the FDA’s viral 2021 public health guidance advising against the use of ivermectin for treating COVID-19. The most notable offending tweet stated, “You are not a horse. You are a not a cow. Seriously, y’all. Stop it.”

Department of Justice trial lawyer, Isaac Belfer, defended the FDA in this suit brought by Drs. Mary Talley Bowden, Robert L. Apter, and Paul E. Marik. On undercover camera, Belfer admits to a Project Veritas journalist that his client’s legal loss was deserved because the agency overstepped its statutory authority when it publicly tweeted medical advice.

Belfer told our journalist, “So, what the agency has done… [is] unquestionably beyond its authority. Making a recommendation of what drugs to take or not to take, that’s the practice of medicine. And FDA can’t practice medicine.”

The FDA’s public relations campaign also failed to inform the public that the award-winning antiparasitic medicine had a decades-long track record of successful medical usage in humans.

During the COVID-19 pandemic, the doctors prescribed ivermectin to tens of thousands of patients and found the drug to be a cheap and effective treatment.

The doctors told Project Veritas that they suspect that the suppression campaign against ivermectin was motivated by the government’s interest in fast-tracking the experimental COVID-19 vaccination. This speedy vaccine roll-out could only be accomplished through the FDA’s emergency use authorization [EUA], and only if no other alternative medications existed to treat COVID-19.

The FDA’s tweets caused a deadly chain reaction. The agency’s pronouncements were swiftly enforced by national medical associations and regulatory agencies, pharmacists refused to fill prescriptions, insurance refused to pay for it, and doctors who prescribed it faced career ruin.

Drs Apter and Bowden told Project Veritas that suppression of ivermectin led to a prolonged pandemic, and potentially millions in excess COVID deaths.

Apter: “It’s not unreasonable to think that there have been a million unnecessary deaths from COVID in the United States because of the public health agency suppression of effective early treatment with repurposed inexpensive medications.”

Bowden: “If more people had access to early treatment in the form of ivermectin, monoclonal antibodies, hydroxychloroquine… we could have nipped the pandemic in the bud.”

As a result of the lawsuit, the FDA was forced to delete its social media posts warning against the use of ivermectin for treating COVID-19. Though the FDA removed its public statements, the agency did not change its policy or directives. Because major state and national medical governing authorities look to the FDA as an authoritative source on the appropriate use of drugs, pharmacies still refuse to prescribe ivermectin, and doctors face professional repercussions for prescribing it.

Dr. Talley Bowden was forced to resign her privileges from Houston Methodist Hospital; Apter was referred to the Washington Medical Commission and Arizona Medical Board for disciplinary proceedings; and Marik was forced to resign from his positions at Eastern Virginia Medical School.

Apter: “Because of my prescription of ivermectin for COVID I am still facing persecution by the medical licensing boards in spite of the fact that they have not been able to show a single adverse event in my care.”

Bowden: “I have a medical board coming after me because I tried to help a patient get ivermectin. We all had professional repercussions because of our use of ivermectin.”

Though the doctors continue to face professional consequences for their advocacy of ivermectin use for COVID-19, Belfer admits that the doctors dealt a significant blow to the government with their court victory. He told Project Veritas that the agency will think twice before issuing any misguided health advice in the future.

“I think going forward they’ll [FDA] probably be a bit more careful. They [the doctors] got an opinion that was good for them. That kind of limited FDA’s authority. It’s not okay to… actually tell people, ‘You should not take this drug.’”

Dr. Bowden says the fight against government overreach was worth it, because now doctors are vindicated in their years-long quest to protect the health of their patients.

Bowden: “One thing this case did is set a precedent. I think it permanently tarnished the reputation of the FDA. I think the public will takes the FDA little less seriously now, and it keeps them from making the same bold, reckless move in the future when it comes to telling patients what they can and cannot do. Like Isaac [Belfer] said, and we have all said, the FDA is not your doctor. The FDA has no business telling patients what they can take. And we proved in the court of law that they cannot do that.”

August 30, 2024 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular, Video, War Crimes | , , , | Leave a comment

Gaza and Polio

By Richard Hugus | August 27, 2024

On July 30, 2024 the Health Ministry of Gaza declared a polio epidemic in GazaThe World Health Organization then said it would send more than a million polio vaccine doses to Gaza. On August 16, according to Al-Jazeera, the first case was reported and the UN’s Antonio Guterres called for a ceasefire to make a vaccination campaign possibleThis call was supported by Hamas.

Health authorities rightly point out that the cause of the horrific health conditions in Gaza is the ongoing Israeli genocide – the bombing of homes and infrastructure, the shelling, the withholding of food and medical supplies, the sadistic evacuations — and the authorities of course call for all these things to end. But the involvement of globalist agencies like the UN and WHO raise suspicions that the polio declaration may be just another attack on the people of Gaza concealed under a cloak of humanitarianism.

According to Al-Jazeera, the announcement of the alleged outbreak came on August 7 from one Dr. Hamid Jafari, a World Health Organization polio specialist who claimed the polio virus was found in wastewater samples in Deir el-Balah and Khan YounisDr. Jafari is currently employed by the US Centers for Disease Control, a deeply corrupt organization which has spent the past three years pushing vaccines for another purported virus – covid 19 – in spite of clear proof from the very beginning of multiple harms caused by the vaccine. This harm is not limited to the US. Denis Rancourt and colleagues have recently offered statistical proof of almost 31 million excess deaths globally for the period 2020-2022, deaths which they attribute to the strangely universal worldwide public health response to covid 19, to include lockdowns, business closures, isolation, harmful hospital protocols, and particularly the mRNA vaccines.

Regarding Dr. Jafari in Gaza, The CDC website tell us that he “is a graduate of CDC’s Epidemic Intelligence Service (EIS) program, class of 1992. . .  currently serving as the Principal Deputy Director, Center for Global Health, at the Centers for Disease Control and Prevention.The website goes on to say that “Dr. Jafari served as the project manager of World Health Organization’s (WHO’s) National Polio Surveillance Project in India from 2007-2012. As the project manager, he was the main technical advisor to the government of India in the implementation of the nation’s large scale polio eradication, measles control, and routine immunization activities, and he directed WHO’s extensive network of more than 2000 field staff.”

Thus Dr. Jafari was in in charge of a vaccination campaign in India where, in one study, researchers found that between 2000–2017 there were “an additional 491,000 paralyzed children” above normal. The ambitious “polio eradication” program in India was funded and led by the Gates Foundation and the WHO. The number of paralysis cases was found to be proportional to the number of vaccine doses administered. The Gates Foundation and WHO are not exactly separate entities – Gates is a major funder of the WHO. Dr. Jafari’s employment at the CDC, his authoritative declaration of a polio epidemic in Gaza, and WHO’s immediate announcement of the shipment of over a million vaccines should raise red flags.

Polio is a condition that is often confused with the catchall “acute flaccid paralysis.”  Acute flaccid paralysis may even be the result of injection of polio “vaccines, but it is not polio. The polio vaccine can and does cause acute flaccid paralysis. From experience in the US since the 1950s it is known that what was often called polio wanot the gut virus that humans have lived with more or less uneventfully throughout history, but a form of paralysis caused by human exposure to neurotoxins introduced in the 20th century — for example, mercury and aluminum adjuvants used in vaccines, leaded fuel, fluoridated water, pesticides and herbicides like arsenic, DDT, dioxin, and glyphosate. DDT was in widespread use in the 1950s. When it was banned, the high numbers of “polio” cases went down. The famous Salk and Sabin vaccines had little to do with it, though the medical establishment claimed victory. Indeed, as we know from what is called “the Cutter incident”  in 1955, vaccines produced by Cutter Laboratories ended up causing 40,000 cases of polio, severely paralyzed 200 children, and killed 10. Later iterations of the vaccine were found to contain a cancer-causing agent called SV-40 (SV being short for ‘simian virus’). Bernice Eddy, the scientist who discovered this, was hounded out of her job at the US National Institute of Health. Lest one think that things are surely more advanced now than in the 1950s, as recently as April 2023 a well-known scientist named Kevin McKernan found SV-40 in samples of the Pfizer covid -19 vaccine. A new term was coined to describe a common effect of the covid injections — “turbo cancer” — perhaps attributable to the SV-40 and the normally forbidden DNA plasmids also found in the samples.

In an emergency involving a projected 2,700 aid workers delivering 1.6 million doses over a short period of time (between bombings), will the parents of the one million children in Gaza be given complete information about the contents of the polio vaccine their children are about to be given? Will there be a full explanation about risks and possible side-effects? Will the parents have any understanding of the negative history of polio vaccines or of vaccines in general? Will they have the informed consent required in any medical intervention? Will they be given redress for any injuries? No, not a chance. The instructions will be “here’s your dose, now move along.” To be fair, it’s the same all over the world.

Dr. Suzanne Humphries is a well-known kidney specialist who spent years of her professional life coming to grips with organized medicine’s ignorance of the fact that vaccines may cause rather than cure disease. She found that high numbers of polio cases mysteriously went away when polio came to be named other things, like poliomyelitis, transverse myelitis, Guillain-Barré syndrome, enteroviral encephalopathy, traumatic neuritis, and Reye’s syndrome. A similar trick was played when influenza suddenly disappeared between 2020 and 2023 and “covid” took its place. Incidentally, one of the common effects of the covid vaccine was facial paralysis, or Guillain-Barré syndrome. Vaccines contain neurotoxins. Neurotoxins cause paralysis and myriad other problems. When it comes to Gaza, we might ask: is the confirmed case there actually polio, or is it one of the many distinct diseases under the umbrella of acute flaccid paralysis? Does a vaccine designed for one strain of polio address some, all, or even any of the mimicking diseases? Is there documentation that the confirmed case was actually polio, or do we just have to take Dr. Jafari’s word for it?

According to Dr. Humphries, “no vaccines are safe. Having “efficacy” means an antibody response is generated, not that they keep you from getting sick. There are many other ways to keep children healthy other than injecting them with disease matter, chemicals, animal DNA, animal proteins, detergents and surfactants that inflame and weaken the blood brain barrier, potentially causing inflammation and other problems.” One way would be to stop bombing them.

The Gaza Health Ministry and Hamas are surely busy enough dealing with zionist genocide, but they need to know that in the last few years public health has been revealed as a very effective weapon of war. The US Department of Defense had a leading role in the worldwide biowarfare operation known as “covid 19 countermeasures.” The WHO and the UN were very much involved in this operation. They are not to be trusted. Like the US government, these supposed humanitarian organizations speak from both sides of their mouth – calling for ceasefire while doing nothing to stop the weapons that every day kill more Palestinians. They know that the best way to protect the children of Gaza is to bring good nutrition, clean water, clean air, housing, and an end to the trauma of psychopath Israel’s daily bombing, yet they do nothing meaningful to bring this about. They are not offering aid with their polio vaccines; they are offering more poison.

August 27, 2024 Posted by | Deception, Science and Pseudo-Science | , | Leave a comment

Court Finds Kennedy Has Standing in Our Consolidated Case

As I predicted, our new co-plaintiff Kennedy meets even the Supreme Court’s stringent standing requirements, the injunction against the government is back in play.

By Aaron Kheriaty, MD | Human Flourishing | August 26, 2024

As I explained in a previous post, Robert F. Kennedy Jr.’s companion lawsuit Kennedy v. Biden has been consolidated by the court into our Missouri v. Biden case. Based upon documents we obtained on discovery, the court recently found that Kennedy meets the Supreme Court’s stringent standing criteria. We only need one co-plaintiff with standing to bring the case and the petition for the injunction. So the injunction is back in play, and we will likely find ourselves at the Supreme Court again in a few months. Unless SCOTUS invents another technicality on which to temporize, they will be forced to rule on the merits of the evidence against the government, which we believe is overwhelming.

On the issue of Kennedy’s standing, U.S. District Court judge Terry Doughty last week ruled: “There is not much dispute that both Kennedy and CHD [Kennedy’s nonprofit Children’s Health Defense] were specifically targeted by the White House, the Office of Surgeon General, and CISA, and the content of Kennedy and CHD were suppressed. Therefore, Kennedy must now show a substantial risk that in the near future, at least one platform will restrict the speech of Kennedy in response to the actions of one Government Defendant.” Citing evidence we uncovered in Missouri v. Biden, Doughty explained: “The Court finds that Kennedy is likely to succeed on his claim that suppression of content posted was caused by actions of Government Defendants, and there is a substantial risk that he will suffer similar injury in the near future.”

As reported in The Kennedy Beacon Substack:

The latest ruling is not only significant for Kennedy but for the future of online speech. In June of this year, the Supreme Court ruled that the state attorneys general of Missouri and Louisiana did not have standing to bring their case on government directed mass censorship. Now that Kennedy and the CHD have been found to have standing in the matter, the Supreme Court will likely have an opportunity to judge the issue on its merits rather than on a technicality as it did when making its standing ruling on an injunction in June.

If Kennedy and his co-plaintiffs are able to demonstrate to judges that the Biden administration’s intrusion into the actions of major social media companies resulted in censorship, the country will be one step closer to a major legal ruling guaranteeing freedom to speak online without the censorious interference of the federal government.


In related news, Kennedy announced Friday that he is suspending his presidential campaign. While he has deep disagreements with Trump on several issues, he is endorsing Trump’s candidacy to advance the key issues on which they have substantial agreements—including stopping government censorship and propaganda. His 48-minute speech announcing this decision was an extraordinary moment in American politics and is worth watching. In addition to discussing the issue of government censorship, which seriously hamstrung his ability to campaign, Kennedy’s remarks focus also on the root causes of the current epidemic of chronic disease in the United States.

While there is online buzz that Trump may tap Kennedy as Attorney General, I anticipate if Trump is elected he will appoint Kennedy to his cabinet as Secretary of Health and Human Services, a department which includes the CDC, FDA, and NIH. This could prove a welcome opportunity for the reform of our public health agencies. I am currently working with a team of policy analysts and health freedom advocates on concrete policy proposals for just such reforms, and will keep you posted on our progress with that project.

August 26, 2024 Posted by | Civil Liberties, Full Spectrum Dominance, Science and Pseudo-Science | , , , | Leave a comment

What Does a Fraudulent Vaccine Safety Study Look Like?

By Dr. William H. Gaunt | The Defender | August 26, 2024

New vaccines should be proven safe before they are accepted onto the Centers for Disease Control and Prevention (CDC) vaccine schedule.

Here is what is actually happening: Vaccine companies are doing studies that claim to demonstrate the safety of new vaccines but are carefully designed and conducted to intentionally hide the toxicity of these vaccines.

To see how this is done, read on.

What does an honest vaccine safety study look like? 

An honest safety study must have a test group that gets the vaccine and a control group that gets a harmless placebo. Injuries and deaths are compared in the two groups.

If the test group has many more adverse events than the placebo control group, the vaccine is not safe.

Most people would be shocked to learn that none of the vaccines on the CDC vaccine schedule have been safety tested in this way.

What does a fraudulent vaccine safety study look like? 

Rule No. 1 for conducting a fraudulent study: Do not have a placebo control group. Here is where the fraud is happening: The “control group” is deliberately given something that is as toxic as the vaccine being tested. It can be an older vaccine or the vaccine ingredients minus the antigen.

The results will show that the injuries and deaths are similar in both groups. That is because they are both receiving toxic ingredients. The new vaccine is then illogically declared safe.

If there is no placebo control group, the toxicity of the vaccine is hidden. This is both clever and diabolical. Can you see it?

The public is unaware of this subterfuge

Turtles All The Way Down: Vaccine Science and Myth” is the most thorough and brutally honest book ever written about vaccines.

The authors tell us on page 81:

“As we have seen in this chapter, vaccine trials are designed and performed in such a way as to ensure that the true extent of adverse events is hidden from the public. There is not a single vaccine in the US routine childhood vaccination schedule whose true rate of adverse events is known.”

Two examples of how unsafe toxic vaccines got on the CDC vaccine schedule

Prevnar-13 (a pneumococcal vaccine) was given to the test group of children and the “control group” was given the older Prevnar vaccine.

Severe adverse events occurred in 8.2% (one out of every 12 children) in the test group. Severe adverse events also occurred in 7.2% (one out of every 14 children) of the control group.

What percent of a placebo control group would have had severe adverse events? Probably 0% because they would have received something harmless. We can’t know because the authors of this study chose not to have a placebo control group.

The Prevnar-13 vaccine was declared “safe” and was approved for use by the U.S. Food and Drug Administration (FDA). You don’t have to be a doctor or scientist to suspect that both the Prevnar and the Prevnar-13 vaccines are unsafe. “Turtles All The Way Down” covers this fraudulent vaccine safety study on pages 60 and 61.

Here is the second example, which the authors describe on pages 77 and 78:

“In one of the DTaP vaccine trials, 1 in every 22 subjects in the trial group was admitted to the hospital. A similar hospitalization rate was also reported in the ‘control group’ (which received the older-generation DTP vaccine).”

Again, there was no placebo control group. Both vaccines appear to be decidedly unsafe yet the newer DTaP vaccine made it onto the CDC vaccine schedule. DTP and DTaP vaccines contain antigens for diphtheria, tetanus and pertussis.

Why is this happening?

Ultimately, the answer is greed. It is enormously profitable to get a vaccine on the CDC schedule. Vaccine companies will do whatever it takes to accomplish this. If it takes a little scientific fraud, so be it.

The vaccine companies are cheating on vaccine safety studies by omitting placebo control groups, thereby lying about the safety of vaccines. The FDA and CDC are complicit because they are doing nothing to stop this fraud.

Corporate capture or regulatory capture

The FDA and CDC are regulatory agencies. The original function of these agencies was to protect the public from dangerous drugs and vaccines.

Unfortunately, these agencies have been captured by Big Pharma. They no longer focus on protecting the public. They focus on protecting and promoting the interests of pharma companies.

Can we compare the health outcomes of vaccinated versus unvaccinated children?

Theoretically, yes but not if we expect our health authorities or pharma companies to do these types of studies. Chapter 6 of the “Turtles” book is titled “The Studies That Will Never Be Done.”

On page 207 the authors tell us:

“No study that compares the health of vaccinated children to that of unvaccinated children has ever been done by the medical establishment.”

If such a study showed that vaccinated children are healthier than unvaccinated children, it would have been published and been headlined in every newspaper and been the lead story on the nightly news. That hasn’t happened. We suspect that such a study has been done internally at the CDC.

The unwanted conclusion that they won’t allow to see the light of day is that unvaccinated children are far healthier than vaccinated children. This study has likely been done and buried instead of published. Such a study is verboten because it would be a disaster for the vaccine companies.

Private studies show that unvaccinated children are healthier

Here are two privately funded studies:

  1. Relative Incidence of Office Visits and Cumulative Rates of Billed Diagnoses Along the Axis of Vaccination” by Dr. Paul Thomas and James Lyons-Weiler, Ph.D.
  2. Analysis of health outcomes in vaccinated and unvaccinated children: Developmental delays, asthma, ear infections and gastrointestinal disorders” by Brian S. Hooker, Ph.D., and Neil Z. Miller.

Another great resource is the book “Vax-Unvax: Let the Science Speak,” by Robert F. Kennedy Jr. and Hooker. They report on many studies where unvaccinated children have better health outcomes compared to vaccinated children.

Science is for sale

The book “Science for Sale: How the US Government Uses Powerful Corporations and Leading Universities to Support Government Policies, Silence Top Scientists, Jeopardize Our Health, and Protect Corporate Profits” by David L. Lewis, Ph.D., tells the story of how corporate profits can frequently trump true science.

This happens in many industries, not just in vaccines. It is not unusual for government agencies to take the side of the corporations. The author was fired from the EPA for revealing details of how this happens.

The health of the public is subverted by powerful corporations in these situations. Does that sound familiar? Lewis doesn’t cover vaccines in his book except in Chapter 7 where he describes how Dr. Andrew Wakefield was unjustly crushed for questioning the safety of the measles-mumps-rubella or MMR vaccine.

Are vaccines the main cause of autism?

If the answer is yes, that would be very bad for vaccine companies. The “Turtles” authors point out on page 209 how our health authorities are trying hard not to find the correct answer to this question:

“Over the past 15 years, dozens of epidemiological studies have been conducted examining the association between vaccines and autism, but not a single one compared the rate of autism in fully vaccinated and fully unvaccinated children.”

If they actually wanted to answer this question, they would do vax/unvax studies. Such studies are easy to do but our health authorities refuse to do them.

Why do health authorities favor epidemiological studies?

The “Turtles” authors provide the answer on page 198:

“Epidemiological studies are the tool of choice for health authorities and pharma companies to maintain a facade of vaccine safety science. They are cheap, relatively simple to conduct, and, above all, their results are easily manipulated.”

It is entirely possible to get an epidemiological study to conclude whatever its authors want it to conclude. These types of studies are not the gold standard.

What caused the drastic decline in infectious disease mortality?

We are supposed to believe that vaccines have been our saviors. Not true. The huge decline in infectious disease mortality was largely due to sanitation, hygiene and improved nutrition (the availability of fresh fruits and vegetables year-round).

The “Turtles” authors make this clear on page 293. They reference a report by the American Institute of Medicine, which states:

“The number of infections prevented by immunization is actually quite small compared with the total number of infections prevented by other hygienic interventions such as clean water, food, and living conditions.”

The claim that vaccines alone saved us is false and our health authorities know it is false.

Below is a simple graph that causes cognitive dissonance in those who believe that vaccines saved us from high rates of infectious disease mortality.

We can clearly see that deaths from measles were reduced to near zero by the interventions mentioned above BEFORE the measles vaccine was introduced.

Similar graphs for other infectious diseases are shown in the book “Dissolving Illusions: Disease, Vaccines, and the Forgotten History” by Dr. Suzanne Humphries and Roman Bystrianyk. The mortality rate for all infectious diseases was dropping rapidly before vaccines were introduced.

Do you smell a rat?

Yes. And it has been dead for quite a while. We have been bamboozled (deceived, cheated, swindled and defrauded).

Vaccines are now doing far more harm than good by causing a huge increase in chronic diseases like autism, asthma, attention-deficit/hyperactivity disorder or ADHD, Type 1 diabetes, learning disabilities, seizures and much more.

It is way past time to use honest unbiased science to sort it out. Imagine what will happen when honest science is applied to vaccine safety studies.

Here is how the ‘Turtles’ authors sum it up

On page 518:

“Science belongs to the people. It belongs to humanity, not to corrupt government agencies and pharmaceutical giants who collude to rewrite the principles of science in order to continue the decades-long cover-up of their crimes against humanity.

“The magnitude of these crimes is enormous — these entities are in way too deep to ever be able to admit any wrongdoing. They will do whatever is necessary to protect the great vaccine hoax. For them, it is a matter of life and death — literally. And so it is for us.”

The lie that vaccines are safe and effective and that serious adverse events are exceedingly rare is still believed by many people — yet trust in pharma and our coopted regulatory agencies is now rapidly eroding. For example, only a tiny percentage of people are continuing to take the COVID-19 vaccine boosters.

Also, the percentage of parents who are choosing to obtain an exemption to vaccines for their children is increasing. This can be done in almost all states.

It is becoming obvious to a growing number of people that we are being intentionally misled regarding vaccines and vaccine safety.

August 26, 2024 Posted by | Book Review, Deception, Science and Pseudo-Science | , , | Leave a comment

Debate: Is A Demonstration Project Really Necessary?

By Francis Menton | Manhattan Contrarian | August 17, 2024

My repeated calls for a Demonstration Project of a zero-emissions electrical grid have led to a spirited debate among knowledgeable commenters. While most back my position, some say that a Demonstration Project is really not necessary and would be a waste of effort.

The gist of the argument of those disputing the necessity of a Demonstration Project is that it is so obvious that a zero-emissions grid powered predominantly by wind and solar generation cannot be achieved that the expense and effort of building an actual physical facility cannot be justified. Before the building of a physical demonstration project there would inevitably be an engineering feasibility study, and such a feasibility study would not get through its first day before everybody involved realized that this could never work. All it would take would be a few back-of-the-envelope calculations using basic arithmetic and the whole endeavor would be sunk.

Regular commenter Richard Greene leads the forces arguing against a demonstration project. From a comment by Richard on my August 10 post:

A good demonstration project that included manufacturing and farming is very likely not needed. A real local utility Nut Zero grid engineering plan on paper would have grid engineers laughing hysterically. The money allocated for backup batteries would be nowhere close to paying for the battery GWh capacity needed. Backup natural gas power plants could do the job, but gas backup is not wanted. . . . 100% wind and solar can never work due to compound energy droughts, wind drought and solar droughts (batteries are far too expensive).

Representative of the pro-demonstration project side is a comment from “dm” on the August 13 post. Excerpt:

Because many people doubt paper analyses, lived experience is a necessary teacher. Thus, demonstration projects are NEEDED to prove the folly of “sustainable” electricity grids. Furthermore, the demonstration projects MUST be in regions heavily populated with nut zero enthusiasts, and ALL costs MUST be paid SOLELY by households, businesses, institutions … located within the demonstration areas.

My natural sympathies here would lie with Richard’s side of this debate. How can spending what would likely be billions of dollars of public money be justified when calculations that I have made or verified myself show that the project will never come close to success?

But then we must look at what is happening in large states and countries that are proceeding toward the stated goal of a zero-emissions grid without ever having had a working demonstration project. In some of these cases (Germany, UK) the wasted resources are now into the trillions, not billions. And at some point the whole effort will inevitably be ended with some kind of hard-to-predict catastrophe (long blackouts? multiplication of consumer costs by a factor of ten or more?). By then, many of the working resources that have made the grid function will have been destroyed and will have to be re-created, at a cost of further trillions.

Consider the case of Germany. Germany is a very substantial country (80+ million people, making it twice the size of California and four times the size of New York), with the world’s fourth largest GDP at over $4 trillion annually. Germany was one of the first to start down the road to a zero-emissions grid back in the 1990s, and formally adopted its “Energiewende” fourteen years ago in 2010. Germany has proceeded farther than any other large country in converting its electricity generation to wind and solar.

And yet, as I look around for information on Germany’s progress toward zero-emissions electricity, I can’t find any concern or recognition that this might not be doable in the end. Perhaps that exists in German language sources that I can’t read. But from anything I can find, it looks like Germany is forging ahead in the blind faith that if only they build enough wind turbines and solar panels at some point they will have the zero-emissions electricity that they crave.

Go to the website of the Umweltbundesamt (Federal Environmental Agency) for the latest information. At least on the electricity front, you will not find any indication that there may be problems in achieving the zero-emissions utopian future:

The “Energiewende” – Germany’s transition towards a secure, environmentally friendly, and economically successful energy future – includes a large-scale restructuring of the energy supply system towards the use of renewable energy in all sectors. . . . [T]he switch towards renewables in the electricity sector has been very successful so far. . . . While in the year 2000 renewables accounted for 6.3 percent of electricity demand only, its [sic] share has been growing significantly over the past years, exceeding 10 percent in the year 2005 and 25 per cent in the year 2013. In 2023 renewable energy sources provided 272 billion kilowatt-hours of electricity and account for 51.8 percent of German electricity demand. With wind power being by far the most important energy source in the German electricity mix.

Some 30+ years into this process, and they’re only up to barely over 50% of their electricity from “renewables.” And while they may claim that “wind power [is] by far the most important source in the German electricity mix,” in fact when you get a breakdown you find that wind and solar together provided well less than 50%. According to solar advocates Fraunhofer Institute here, in 2023 “biomass” provided some 42.3 TWh of Germany’s electricity (about 8%), hydro provided 19.5 TWh (about 4%), and “waste non-renewable” (I think that means burning garbage) provided 4.5 TWh (about 1%). That leaves under 40% for wind and solar.

If they keep building solar and wind facilities, and expect batteries to be the backup, has anybody calculated how much battery storage they will need? Not that I can find. Here is a website of a company called Fluence, which is an affiliate of German industrial giant Siemens. They excitedly predict a rapid expansion of grid storage in Germany:

Storage capacity will grow 40-fold to 57 GWh by 2030.

Wow, a 40-fold increase! It may sound like a lot. But Germany’s average electricity demand is about 50 GW, so the 57 GWh of battery storage in 2030 will come to about 1 hour’s worth. Competent calculations of the amount of energy storage needed to back up a predominantly wind/solar grid run in the range of around 500 to 1000 hours.

Here from another website is a chart of the growth of energy storage in Germany up to this year.

Look at that acceleration! But the 10 GWh of storage that they currently have will last no more than about 10 minutes when the wind and sun quit producing on a calm night.

In short, this large and seemingly sophisticated country is completely delusional, with no sane voices anywhere to be heard. A demonstration project that fails spectacularly is the only thing with any hope of saving them.

August 25, 2024 Posted by | Malthusian Ideology, Phony Scarcity, Science and Pseudo-Science | , | Leave a comment