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Chinese Scientists Propose Magnetic Launcher on Moon to Send Resources to Earth – Reports

Sputnik – 18.08.2024

BEIJING – Chinese scientists proposed building a magnetic launcher on the Moon, which could become an cost-effective way to deliver resources mined on the lunar surface to Earth, and, in addition, part of the Russian-Chinese lunar station project, Chinese media reported on Sunday.

According to the publication, scientists from the Shanghai Institute of Satellite Engineering suggest that the magnetic levitation installation will work on the same principle as the hammer throw in athletics, but the rotation at increasing speed will be carried out before a cargo capsule is sent to Earth.

Scientists are convinced that, due to the unique environmental conditions on the Moon, such as high vacuum and low gravity, payloads can be sent twice a day, and the cost of such transportation will be about 10% of the cost of existing methods.

“The system’s technical readiness is relatively high. Since it consumes only electricity and does not require any propellant, it will be relatively small in scale and straightforward to implement,” the scientists said in their paper.

They also noted that the main task will be the extraction of helium-3 to help solve the problem of the energy crisis on Earth. The project, in their opinion, will also contribute to the development of space mining technologies, heavy launch vehicles and artificial intelligence.

The proposed launch system will use a 50-meter-long rotating arm and a high-temperature superconducting engine to launch capsules with mined resources. Ten minutes after launch, the rotation speed of the arm will reach the second cosmic velocity of the Moon of 2.4 kilometers per second and about one-sixth of the second cosmic velocity of Earth — and put it on the correct trajectory for returning to Earth.

The system is designed to last at least 20 years, but it will weigh about 80 tonnes, so before it can be delivered to the Moon, it will be necessary to wait for the start of operation of the Chinese super-heavy launch vehicle, the publication said.

The team working on the project suggested that it could be part of a proposed joint Russian-Chinese project to build a research station at the south pole of the Moon by 2035.

The intergovernmental Russian-Chinese agreement on the joint creation of the International Scientific Lunar Station (ISLS) was signed on November 25, 2022. Russian President Vladimir Putin signed a law ratifying the agreement on June 12, 2024, and it entered into force on July 18. The document was published on July 25. It indicates that the station will be created in three phases and will receive modules both on the surface of the Earth’s natural satellite and in its orbit. During the third phase, it is planned not only to study and develop the Moon, but also to assist other countries in landing on the Moon. The implementation dates for each of the phases are not yet mentioned.

August 18, 2024 Posted by | Science and Pseudo-Science | , | Leave a comment

UK rejects payment to Covid-19 jab victims for not being ‘disabled enough’ – Telegraph

RT | August 18, 2024

Almost 14,000 people in Britain have applied for payments from the government for disabilities they claim were caused by Covid-19 vaccines, The Telegraph has reported.

Only 175 people, or less than 2% of those seeking compensation, have so far received a one-off money transfer of £120,000 ($155,300), the paper said in an article on Saturday.

Data obtained by The Telegraph through Freedom of Information requests indicates that those who were eventually reimbursed suffered from conditions such as stroke, heart attack, dangerous blood clots, inflammation of the spinal cord, excessive swelling of the vaccinated limb, and facial paralysis.

Around 97% of the satisfied applications were related to the Oxford-AstraZeneca Covid-19 vaccine, developed by Oxford University and British-Swedish company AstraZeneca, and the rest to the US-made vaccines from Pfizer and Moderna, it said.

The outlet noted that the UK government continued to recommend the AstraZeneca vaccine, despite its use being halted in Germany, Italy, France, and other European countries by March 2021, amid reports of a growing number of blood clotting cases.

Thousands of people have been refused payment due to the government’s medical assessors arguing that there is no concrete proof that their health problems are a result of the vaccines, the report read.

Hundreds of others were turned down due to being “not disabled enough,” it added. Under the rules of the Vaccine Damage Payment Scheme (VDPS), an applicant has to be at least 60% disabled to qualify.

A spokesman for AstraZeneca told The Telegraph that its vaccine “has continuously been shown to have an acceptable safety profile and regulators around the world consistently state that the benefits of vaccination outweigh the risks of extremely rare potential side effects.”

As for the health complications caused by the vaccine, the spokesman said, “our sympathy goes out to anyone who has lost loved ones or reported health problems.”

In May, AstraZeneca, which officially admitted that its vaccines could cause blood clots in certain cases, began the withdrawal of its product worldwide, saying that newer vaccines adapted to the latest coronavirus variants were more effective.

Around 16,000 people have sought payments since the introduction of the VDPS in 1979, with most of the claims related to Covid-19 vaccines. The growing workload resulted in an increase of the staff responsible for handling applications from four people to 80 last year. “We continually review our processes to further develop the way in which we manage claims, and to provide a better service for claimants,” a National Health Service spokesperson said.

August 18, 2024 Posted by | Science and Pseudo-Science | , | Leave a comment

Health Officials Push Whooping Cough Vaccine Amid Uptick in Cases, But Scientists Say Shots Don’t Prevent Transmission

By Suzanne Burdick, Ph.D.John-Michael Dumais | The Defender | August 14, 2024

Public health officials are urging families to get vaccinated against whooping cough, citing an uptick in cases, particularly among adolescents. However, critics say the vaccine doesn’t prevent transmission and contains dangerous toxins that may harm human health.

Connecticut Department of Public Health Commissioner Manisha Juthani said that there were 111 confirmed cases of pertussis in the state so far in 2024 — nearly a 10-fold increase compared to 2023, NBC Connecticut reported this week.

Juthani told The Hour that public health officials are concerned the spread will increase when school begins in just a few weeks.

“We are raising attention to this, both to providers and to families,” she said, “so that theoretically, people can get back up to date on their vaccines before children potentially are going back to day care, are going back to school.”

Other states, including New York and Pennsylvania, have also seen an uptick in whooping cough cases this year, Newsweek reported in early June. Outside the U.S., the United Kingdom and Australia have also reported increases.

Whooping cough, also known as pertussis, is a highly infectious respiratory tract infection, according to the Mayo Clinic. Deaths from it are rare and typically occur in infants.

It’s caused by a bacteria called Bordetella pertussis, according to the Centers for Disease Control and Prevention (CDC).

The CDC recommends that “everyone” — from babies as young as 2 months old to adults, particularly pregnant women — vaccinate against the illness by getting either a DTaP or Tdap vaccine, which also ostensibly protect against tetanus and diphtheria.

According to the CDC, the vaccine is “the best way to prevent whooping cough.”

Pertussis can be treated with antibiotics

However, Karl Jablonowski, Ph.D., senior research scientist at Children’s Health Defense (CHD) told The Defender the pertussis vaccine may contribute to the spread of the infection — because it doesn’t prevent transmission.

“The pertussis vaccine is one of those that breaks the mold of what we think a vaccine is,” Jablonowski said. “Pertussis is probably the best case I can think of for a vaccine that does not prevent transmission.”

He added, “Every time there is a case of it, health officials will get on TV urging people to get vaccinated — wrongfully believing it will stop transmission.”

As The Defender recently reported, the CDC has been tracking changes in the prevalence of bacteria causing whooping cough for years.

Although the CDC’s whooping cough website still says the illness is caused by Bordetella pertussis, the most recent CDC data found that the Bordetella parapertussis type of whooping cough has significantly overtaken Bordetella pertussis in prevalence — and according to research published in Vaccines in March, the existing vaccines “scarcely provide protection” against this strain.

Brian Hooker, Ph.D., CHD chief scientific officer, told The Defender pertussis can be treated with antibiotics — “erythromycin and azithromycin are standard,” he said — and high doses of vitamin C.

The CDC’s website acknowledges whooping cough can be treated with antibiotics and fails to explain why the agency favors vaccination over antibiotics.

Pertussis vaccine may prevent herd immunity

Earlier this year, Jablonowski spoke on the poor efficacy and high-risk profile of the pertussis vaccine before Tennessee lawmakers as they weighed a bill to prohibit the state’s Department of Children Services from “requiring an immunization as a condition of adopting or overseeing a child in foster care if an individual or member of an individual’s household objects to immunization on the basis of religious or moral convictions.”

During March testimony before the Tennessee General Assembly Civil Justice Committee, Jablonowski cited scientific studies that debunk the notion that the vaccine is the best way to prevent whooping cough.

For instance, a 2016 review published in JAMA that reviewed more than 10,000 whooping cough cases found that more than half the cases in the five largest statewide outbreaks occurred in individuals who were partially or fully vaccinated against pertussis.

A 2019 review published in the Journal of the Pediatric Infectious Disease Society concluded that “all children who were primed by DTaP vaccines will be more susceptible to pertussis throughout their lifetimes, and there is no easy way to decrease this increased lifetime susceptibility.”

Another review, also published in 2019, concluded that pertussis vaccines “do not reduce the circulation of B. pertussis and do not exert any herd immunity effect.”

Jablonowski told lawmakers that not only does the pertussis vaccine not “exert” a herd immunity effect, but the vaccine “has a negative effective on herd immunity.”

He explained:

“A vaccinated person can asymptomatically carry and transmit the disease, and cannot then learn how to fight it naturally.

“If you accept that in order to achieve herd immunity 90% of the population needs to not retransmit the bacteria once exposed to it, then once you have vaccinated more than 10% of the population herd immunity becomes impossible, as the vaccinated citizens will be contracting and transmitting the disease.”

Jablonowski told The Defender the only two scenarios in which getting the vaccine might protect someone else is when it’s given during pregnancy or to a nursing mother.

According to the CDC, pregnant women should get the Tdap vaccine to provide their babies with the “best protection” from whooping cough, ideally between 27 and 36 weeks gestation. Protective antibodies pass from the pregnant woman’s body to the fetus, the agency said.

Researchers funded by the pharmaceutical company Sanofi — which sells pertussis vaccines — in 2022 published a statement saying that vaccination against pertussis during the second or early third trimester of pregnancy is “highly protective” against pertussis in young infants.

Both the CDC and Jablonowski said that vaccinating nursing mothers doesn’t appear to be effective in protecting babies from whooping cough.

A 2012 study conducted in a Houston area hospital found that giving postpartum moms the Tdap vaccine didn’t reduce the number of infections in babies when compared to prior years in which the hospital didn’t readily give the vaccine postpartum.

The hospital implemented a standing order that all new mothers get Tdap, Jablonowski said.

The researchers looked at health data from moms and babies 7.5 years before and almost 1.5 years after this standing order, he said. “Cases of infant pertussis practically doubled and the mortality rate practically tripled” after the standing order.

Vaccine contains aluminum and formaldehyde

Both of the two current formulations of the pertussis vaccine contain toxins known to harm human health, including aluminum and formaldehyde, Jablonowski told the lawmakers.

Aluminum is a known neurotoxin that can affect more than “200 important biological reactions” and cause “negative effects on [the] central nervous system,” according to a 2018 paper published in the Journal of Research in Medical Sciences.

Formaldehyde is a known carcinogen that is toxic to the respiratory system, central nervous system, optic nerve, kidney, liver, testicles and other body systems.

The pertussis vaccine, typically administered as part of combination vaccines like DTaP or Tdap, contains several other potentially harmful ingredients. These typically include inactivated B. pertussis toxin and several of its components, polysorbate 80, gluteraldehyde, 2-phenoxoyethanol and in some cases, trace amounts of mercury, according to the National Vaccine Information Center (NVIC).

Some researchers suggest the chemically inactivated pertussis toxin in DTaP may retain some bioactivity, potentially inducing brain inflammation in certain individuals.

CDC didn’t follow up on 2012 report on adverse events following DTaP/Tdap vaccines

For the past 70 years, researchers have used the pertussis toxin in animal studies to purposefully trigger various physiological responses. Responses include heightened sensitivity to histamine, serotonin and endotoxins. Researchers also used the pertussis toxin to induce experimental autoimmune encephalomyelitis.

The toxin’s ability to penetrate the blood-brain barrier under certain conditions has long been a concern. This property makes brain inflammation, or encephalitis, and its potential for lasting neurological damage a particularly severe complication associated with both whooping cough infection and pertussis vaccination.

According to the Vaccine Adverse Event Reporting System (VAERS), from 1990 to 2024, there were 190,994 injury reports following pertussis-containing vaccines, including 3,377 deaths, according to NVIC. Over 85% of these deaths occurred in children under age 3.

While this data includes pre-1996 reports, when the whole-cell pertussis portion of the DTP vaccine formulation was changed due to its serious side effects, it’s important to note that a significant portion would be related to the DTaP vaccine given its widespread use since 1996.

Over 6,000 claims for injuries from pertussis-containing vaccines were submitted to the federal Vaccine Injury Compensation Program (VICP) as of Aug. 1, 2024. The cases include 872 deaths and over 5,000 serious injuries. Pertussis-containing vaccines comprise the highest number of VICP death claims and the second most compensated vaccine injury claims.

A 2012 study published in JAMA found an increased risk of febrile seizures in children 3-5 months old on the day of or day after receiving the first two doses of DTaP-containing vaccines.

The Institute of Medicine’s (IOM) 2012 report, “Adverse Effects of Vaccines: Evidence and Causality,” evaluated 26 reported adverse events following DTaP/Tdap vaccination. They included encephalopathy, encephalitis, chronic hives, autism, sudden infant death syndrome, arthritis, Guillain-Barré syndrome, diabetes mellitus, immune thrombocytopenic purpura, transverse myelitis and others.

For 24 of the 26 adverse events, the committee said there was not enough data either to support or reject vaccine-related causality, primarily due to a lack of adequate studies.

To date, the CDC has not conducted any additional studies in response to IOM’s recommendations, according to the authors of “Vax-Unvax: Let the Science Speak,” Hooker and Robert F. Kennedy Jr., CHD’s chairman on leave.

A 2017 study led by Dr. Anthony Mawson published in the Journal of Translational Science, compared the health outcomes of vaccinated and unvaccinated children ages 6-12. The study found that while vaccinated children had fewer cases of chicken pox and pertussis, they had significantly higher rates of other health issues.

According to the study, vaccinated children were more likely to be diagnosed with allergic rhinitis, eczema and neurodevelopmental disorders. The vaccinated group also showed higher rates of attention-deficit/hyperactivity disorder, autism, learning disabilities and chronic health problems.

Additionally, the study reported that vaccinated children had a higher incidence of pneumonia and ear infections compared to unvaccinated children.

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.

August 17, 2024 Posted by | Deception, Science and Pseudo-Science | , | Leave a comment

The American Board of Internal Medicine Revoked All 3 Of My Board Certifications

Although I can still practice medicine, the ABIM’s actions against me and Paul Marik threaten the sanctity and autonomy of the physician-patient relationship.

Pierre Kory’s Medical Musings | August 17, 2024

I will just start by saying that I believe that the ABIM’s decision was 100% predetermined even before we first received their accusation in June 2022. There was no way they were going to declare us innocent of misinformation, even though a good portion of this country knows how effective and accurate our deeply evidence-based Covid treatment guidance was (and still is).

One of the reasons why they were never gonna let us off is that, if they declared us “innocent,” (i.e. accurate) that action would have immediately imperiled the decisions by medical boards across the country who persecuted hundreds of doctors for using ivermectin or hydroxychloroquine or for recommending against Covid-19 mRNA gene therapy products. More importantly, it could potentially launch hundreds of thousands of lawsuits by the families of patients who died due to lack of early treatments offerred by clinics and hospitals or filled by pharmacies.

The above examples which led to the deaths of so many shows the sheer power of mega-corporations that put their financial interests ahead of our health and our lives. Through their overwhelming influence over nearly every institution of society and Science (media, journals, health agencies, politicians, medical schools, physicians etc), they literally succeeded in depriving a whole country (and world) of the most effective, inexpensive, safe, and widely available treatments for Covid. My biggest worry is that this crime against humanity may never enter the history books and thus will be eventually erased from memory. Which is looking probable.

The massive financial opportunities that Covid immediately presented to Big Pharma were threatened by the “inconvenient truths” Paul and I put out there. This ABIM action is one way in which Big Pharma punishes those who are foolish enough to do so. Foolish is not quite the right word in our case as I would argue we were simply naive to the consequences of advocating publicly for the use of off-patent medicines for an immensely profitable disease. It wasn’t heroism as some think, but rather extreme naivete.

I really never thought I would have to lose/leave three jobs and now three Board certifications for speaking truths. Recall that I was very well known in my specialty prior to Covid and was about to become Full Professor when I resigned as Chief of the Critical Care Service at the University of Wisconsin (where I was also the Medical Director of the Trauma and Life Support Center). Reading the Washington Post article “Doctors Accused of  Spreading Misinformation Lose Certification” was a pretty sobering reminder of how far I have supposedly “fallen” (Not so fun fact: they completely overstated my salary as the money I received in 2022 included retroactive pay for 2021).

But I am still standing folks. I am happily practicing medicine at my Leading Edge Clinic with my amazing partner Scott Marsland. As many know, we specialize in treating vaccine injury syndromes and Long Covid, and I believe we are soon closing in on having treated our 1,400th patient.

Thank God I managed to build a private, fee-based practice two and half years ago. At the time I suspected this was coming while also already aware that I was “unemployable” by the system. I got fired by my last hospital for a 100% made up complaint, despite the fact they desperately needed me. I was an independent contractor at the time and my ICU partners and all the nurses really liked me. But my partners were telling me that they were under increasing pressure by the Chief Medical Officer to “get rid of Kory.” Although they initially resisted, my stance on vaccines started to cause even more problems for them. When the ICU Director, who was both a friend and a colleague, called to fire me, his last words were, “Pierre, I know there is a war going on and unfortunately you are a casualty.” Truer words were never spoken.

Just know that Board certification is not a license to practice medicine (that comes from state medical licensing Boards of which I have more than a few still). But this ABIM action now puts a definitive end to any hope of me returning to an academic or “system” position (not that I have that hope anymore). Why is that? Well, because Board Certification was originally just a badge of distinction that doctors could use to impress each other and their patients. But they have since weaponized and monetized Board Certification in that currently you cannot obtain a faculty appointment at an academic medical center without one. Nor can you work for most hospitals without one. Even worse, insurance plans will not put you on their provider panels without it. So, although I have been fully excommunicated from “the system,” I cannot be happier about it.

Understand that what happened to me this week was a devastating censorship action, plain and simple. It was done for two reasons; the first was to destroy my reputation and credibility so that my voice will no longer carry (essentially silencing me) and the other was to send a message to doctors that if they stray from consensus, no matter how scientifically absurd (e.g. mRNA vaccines for a coronavirus), dangerous (e.g. remdesivir, mRNA jabs), or ineffective (Paxlovid), they will be punished.

The damage that will result to patients again, is incalculable. No longer will “system” doctors be able to practice medicine with the autonomy they require to arrive at the best decision for each individual patient. Nearly everything they do will be protocolized with society guideline recommended treatments (i.e. consensus manufactured by Pharma). No longer will they be able to “think out of the box” or use treatments which although known effective, do not have the blessing of those in control of that system. I am as terrified as ever of needing a hospital.

Not to overstate the importance of their actions, but Medicine as I knew it, or thought I knew it, is even more dead if that is possible. If you can’t have a differing scientific opinion without losing your career over it, then how is that Medicine or Science? In fact, in our repeated written defenses, we challenged the ABIM, asking them where “the line” is between legitimate scientific debate driven by a differing emphasis on or interpretation of data and outright misinformation.

Misnformation, as I understand it, is defined as “incorrect or misleading” information. For us to be misinformationists, in my mind, would mean that all the data from trials and studies that exist for therapeutics in Covid;

  1. the overwhelming preponderance of data for the efficacy and safety of ivermectin in Covid shows it to be ineffective and dangerous
  2. the overwhelming preponderance of data for the vaccines show they are safe and effective

Basically, it comes down to how you interpret the body of evidence which currently exists. Paul and I adhered rigidly to a “totality of the evidence” approach, drawing from in-vitro, in-vivo, clinical and epidemiologic data. All of it lined up in a truly magnificent, inspiring, and unprecedented way. Well, except for the “Big 7 RCT’s” which manipulated the design, conduct and analyses to conclude ivermectin was ineffective. I spent literally hundreds of hours (along with others like Alexandros Marinos), publishing critiques which exposed the most absurd scientific misconduct I had ever witnessed. If interested, here are just some of those critiques, e.g. Oxfords’ PRINCIPLE trial, the TOGETHER trial (three parts, herehere, and here, and the NIH ACTIV-6 trial )

We also evolved with the data, unlike the agencies who had quickly determined in December of 2020 that the vaccines were safe and effective and never, ever veered from that stance up until this day. In contrast, the founding members of the FLCCC, for quite a long time, differed in respect to the efficacy, safety, and need for the mRNA vaccines. I was the first and most vocal against the mRNA vaccines (starting in April 2021) which actually almost led to the breakup of the FLCCC or at least the membership of the original 5.

Prior to April 2021 I was simply neutral/skeptical. That skepticisim was due to what I thought might be folly in trying to vaccinate against a coronavirus (I knew that historically coronavirus vaccines had failed because the vaccinated animals developed antibody dependent enhancement and also that coronaviruses mutate rapidly). Then I did my first deep dive on VAERS and the epidemiologic data showing massive spikes in mortality and hospitalizations timed with the rollout of the jabs across dozens of countries. Voila, I was now “anti-vaxx.”

I continued to track and analyze the ever-emerging data and the horrors they revealed. This work ultimately led the FLCCC to reach an internal “consensus” that the vaccines should be avoided at all costs (literally at all costs as none of the costs incurred by taking the jab were worth someones life). Anyway, I just wanted to show that we evolved with the data, always questioning and reviewing as new data emerged.

I will end by reminding all of how dangerous the ABIM’s actions will be to all of our lives because it will further erode and/or literally destroy the patient-physician relationship. As I wrote in a previous Op-ED in the Daily Caller on January 31, 2023, “A War Is Still Being Waged Against Doctors Who Question Covid Orthodoxy:”

By virtue of their professional training, doctors must advise patients on available treatments and known risks of any treatment or procedure. By threatening doctors who might provide information different than their preferred worldview, ABIM is disrupting the doctor-patient relationship.

When allowed to practice their craft freely, physicians can prevent societal disaster by focusing on individual patients, informed by clinical experience.

Groups like the ABIM, and public medical officials like Fauci, should support and encourage evidence-based debate and patient-centered care.

Instead, they have suppressed both that debate and treatment approach by persecuting its proponents. This campaign must be stopped, its origins and evolution must be thoroughly documented, and it must never be allowed to recur. Physician autonomy must be restored lest all patients suffer.

August 17, 2024 Posted by | Civil Liberties, Full Spectrum Dominance, Science and Pseudo-Science | , , , | Leave a comment

‘Medical Warfare’: Doctors Who Questioned COVID Shots, Promoted Ivermectin Lose Certification

By Michael Nevradakis, Ph.D. | The Defender | August 14, 2024

Two doctors who spoke out about vaccines and alternative treatments for COVID-19 received notice that their medical certifications were revoked, while another doctor said her certification was revoked without her knowledge.

The American Board of Internal Medicine (ABIM) last week revoked the certifications of Drs. Pierre Kory and Paul Marik, following a two-year investigation into their promotion of ivermectin and hydroxychloroquine as treatments for COVID-19 and their statements questioning the safety and efficacy of COVID-19 vaccines.

According to The Washington Post, the two physicians continued “to promote ivermectin, an anti-parasitic medication, as a treatment for COVID long after the medical community found it to be ineffective.”

Kory and Marik are co-founders of the Front Line COVID-19 Critical Care Alliance (FLCCC), which promotes alternative treatments for COVID-19.

Citing unnamed experts, the Post claimed the FLCCC “spread misinformation about the coronavirus pandemic.”

MedPageToday quoted an ABIM spokesperson, who said the organization “does not comment publicly on the reasons for the revocation of certification.”

However, in a summary of the ABIM’s decision reviewed by The Defender, the organization stated that the doctors’ “conduct poses serious concerns for patient safety and undermines the trust that the public and the medical profession place in the meaning of ABIM board certification.”

In a press release, the FLCCC Alliance said it “categorically disagrees” with ABIM’s decision.

“We believe this decision represents a dangerous shift away from the foundational principles of medical discourse and scientific debate that have historically been the bedrock of medical education associations,” the press release states.

Marik told The Defender :

“The bottom line is we’re disappointed because we stand up for the truth. To censor science is to censor progress. Science is based on dialogue and people can have different points of view. That is the principle of science: it’s people having different points of view.

“We’ve never been in a situation before where physicians who have opposing points of view are silenced … It sets a really bad precedent that you can’t really challenge the status quo, and as we know, in medicine, there have been very dramatic changes based on changing understandings of science.”

In the FLCCC Alliance press release, Kory said, “This fight is about more than just our right to speak — it’s about protecting the future of healthcare. When doctors are silenced for questioning the prevailing narrative, we all lose.”

Kory and Marik participated in an ABIM hearing in May, but internist Dr. Meryl Nass, founder of Door to Freedom, told The Defender that ABIM revoked her certification without her knowledge.

Nass said she was blindsided by ABIM’s decision to revoke her license, which she said she found out about only when she searched for herself in the organization’s database of certified physicians.

Nass told The Defender :

“After the Maine Medical Board suspended my license illegally — even though none of my alleged transgressions met the statutory requirement for an immediate suspension — the board later found me guilty of things I had not done and continued the suspension … All of this with never a single patient complaint.

“Now I learn, by chance, that the ABIM has suspended me without ever informing me I was even under an investigation, which is illegal according to the ABIM’s process.”

Dr. Peter McCullough also faced similar difficulties with the ABIM over his positions on COVID-19 vaccines and treatments. According to MedPageToday, ABIM revoked his certifications in 2022 — although, as of today, ABIM lists him as certified.

McCullough told The Defender, “The ABIM is violating principles of equal protection, due process, rules of evidence and has gone ex post facto to find reasons to attack qualified ABIM-certified doctors who innovated and saved lives early in the pandemic.”

Science based on ‘different points of view’

Kory and Marik held ABIM certifications in internal and critical care medicine, while Kory was also certified in pulmonary disease, according to MedPageToday.

They were initially notified about the risk of losing their certification in May 2022. Last year, ABIM’s Credentials and Certification Committee recommended the revocation of their certification for disseminating “false or inaccurate medical information.” A hearing followed in May.

According to the FLCCC Alliance’s press release, Kory and Marik “tirelessly defended their positions.” However, despite “presenting over 170 references in a detailed 60-page response submitted in January 2023, the ABIM has chosen to dismiss these robust scientific contributions in favor of a narrow, ‘consensus-driven’ narrative.”

According to the summary of ABIM’s decision, Kory and Marik’s “statements about the safety and efficacy of ivermectin and hydroxychloroquine” as treatments for COVID-19 “are false and inaccurate because they are unsupported by factual, scientifically grounded, and consensus-driven medical information.”

The ABIM also addressed the doctors’ positions on the COVID-19 vaccines:

“[The doctors’] statements about the purported ineffectiveness and dangers of COVID-19 vaccines are false and inaccurate because they are unsupported by factual, scientifically grounded, and consensus-driven medical information. …

“There is extensive factual, scientifically grounded, and consensus-driven medical information demonstrating that the COVID-19 vaccines are safe and effective, and lead to better health outcomes.”

Marik questioned the board’s assertions regarding ivermectin, hydroxychloroquine and the vaccines.

“What they do is, they cherry-pick articles which support their point of view and then they go on to say the vaccine is safe and effective. We know that’s completely not true. There’s overwhelming data to question both the safety and efficacy of the vaccine,” Marik added.

McCullough said:

“ABIM never updated its members on important risks such as fatal vaccine adverse events, including myocarditis, nor failing theoretical efficacy necessitating boosters that skipped human testing altogether.

“Setting a new dark milestone, ABIM is decertifying highly qualified physicians for nonclinical reasons and ignoring the evidence for early therapeutics and COVID-19 vaccine safety.”

ABIM engaging in ‘medical lawfare’

According to the Post, Kory maintains a license to practice medicine in California, New York and Wisconsin, where “there are no disciplinary actions listed against him.” Marik has retired and his medical license expired in 2022.

Revocation of their ABIM certification “effectively prevents them from practicing at large hospitals and academic institutions,” the Post reported.

Marik and Nass outlined the difficulties of practicing medicine without certification.

“It doesn’t affect us directly, but it affects us indirectly because we’re being accused of committing offenses that are just not true,” Marik said. “The indirect impact to our reputation … it’s a slap in the face, basically, for all the hard work we’ve done.”

Accusing the ABIM of being part of the “medical-industrial complex,” Marik said, “They seem more interested in making money than in protecting physicians. There have been a number of lawsuits against ABIM, so they don’t have the best of reputations. But unfortunately, they are the main certifying organization in the U.S., so they have enormous power and leverage.”

“If I get my license back — a big if, without board certification, I would have great difficulty getting hospital privileges and collecting insurance reimbursements. In other words, I would be unemployable, though I could potentially work on my own if patients paid me directly,” Nass said.

In 2021, ABIM and the Federation of State Medical Boards collaborated to draft the statement used to discipline Nass.

Nass said organizations like ABIM are engaging in “medical lawfare.” She said they are:

“Creating crimes that do not exist, using procedures that do not exist, to try and silence people like me. What did I do wrong? I read the literature and told the truth about what it said, publicly. The COVID vaccines are very dangerous. They don’t prevent COVID. Drugs can effectively treat COVID. And I prescribed those drugs and helped hundreds of Maine citizens. That was my crime.”

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.

August 16, 2024 Posted by | Science and Pseudo-Science | , | Leave a comment

Whistleblower Will Appeal After Federal Court Dismisses Lawsuit Alleging Fraud in Pfizer COVID Vaccine Trials

By Michael Nevradakis, Ph.D. | The Defender | August 13, 2024

For the second time, a federal court in Texas has dismissed a whistleblower lawsuit alleging Pfizer and two of its contractors manipulated data and committed other acts of fraud during clinical trials for the Pfizer-BioNTech COVID-19 vaccine in 2020.

In his Aug. 9 ruling, District Judge Michael J. Truncale sided with the U.S. government, ruling the government had demonstrated “good cause” to intervene and dismiss the case. He wrote:

“The Government’s desire to dismiss the case — because of its doubt as to the case’s merits, differing assessment of the Pfizer vaccine data, desire to avoid discovery and litigation obligations, and belief that it should not have to expend resources in a case that is contrary to its public health policy — constitutes good cause to intervene.”

Whistleblower Brook Jackson filed the lawsuit against Pfizer, Ventavia Research Group — which conducted some of the clinical trials for Pfizer’s COVID-19 vaccine — and Pfizer contractor ICON PLC in January 2021. Jackson’s complaint was most recently amended in October 2023.

Jackson, a former Ventavia employee, alleged the companies committed numerous violations of the False Claims Act (FCA) during the clinical trials.

According to the lawsuit, the three companies “deliberately withheld crucial information from the United States that calls the safety and efficacy of their vaccine into question,” thus defrauding the federal government, which purchased the vaccines.

The FCA allows the government or a party suing on its behalf to attempt to recover money for false claims made by parties to secure payment from the government.

The FCA also allows whistleblowers to be rewarded for confidentially disclosing fraud that results in a financial loss to the government.

While whistleblowers have the right to sue under the FCA, the federal government can choose to intervene in the case at a later date. In Jackson’s lawsuit, the U.S. government initially declined to intervene in February 2022. However, in March, the government filed a motion to intervene and to dismiss the case.

Attorney Warner Mendenhall, one of the lawyers representing Jackson, questioned whether the U.S. government’s “public health policy” is tolerant toward allegations of fraud during clinical trials for vaccines.

In an interview Monday with Sasha Latypova, a former pharmaceutical industry executive with 25 years of experience in pharmaceutical research and development, Mendenhall said:

“What’s the public health policy of the United States? To kill people and damage people and injure people and make them sick? If that’s the public health policy, well then yes, we’re inconsistent with that.”

Latypova told The Defender she was “not really surprised” by the ruling, noting that drugmakers enjoy legal immunity afforded by emergency use authorization granted by the U.S. Food and Drug Administration (FDA). Latypova described this immunity as a “legal cage.”

She said “The court took as evidence an unsubstantiated opinion of two government bureaucrats … published in an editorial article of a medical journal,” but did not consider the extensive evidence of wrongdoing Jackson provided.

The government’s motion to dismiss cited a Jan. 5 JAMA editorial authored by FDA Commissioner Robert Califf and the FDA’s Center for Biologics Evaluation and Research Director Peter Marks, claiming that “data from various studies” show that “tens of millions of lives were saved by vaccination.”

During his interview with Latypova, Mendenhall argued the government failed to demonstrate good cause and that last week’s ruling did not name any specific examples of this. He said:

“If you read the actual document, there’s no cause listed at all. In fact, the judge has a footnote saying, ‘There is no cause here, but I’m going to look at this other motion I think I can find’ … that’s not how courts are supposed to proceed. You look at the motion first to intervene for good cause. If it’s not there, you’re done. You don’t get to go on and look at the motion to dismiss for hints that maybe there is good cause.”

The ruling also stated that Jackson “failed to allege that she complained to Ventavia or the FDA about fraud against the government.” Accordingly, her claims don’t “rise to the level of protected activity” as a whistleblower.

Mendenhall told Latypova this poses “constitutional concerns” and may have “a chilling effect on other whistleblowers.”

Jackson has 30 days to appeal the ruling, and plans to, Mendenhall said.

“I am very confident we’re going to win that case and get, at least, the retaliation [claim] vindicated, and vindicate what she did as a conscientious citizen of the United States,” Mendenhall said.

Jackson fired within six hours of submitting claims to the FDA

Ventavia, which operated several sites where it conducted clinical trials on behalf of Pfizer, hired Jackson in September 2020.

That same month, Jackson reported problems she observed with the Pfizer vaccine trial to the company’s management. When management didn’t respond, she took her claims to the FDA on Sept. 25, 2020. Ventavia fired her later that day.

Jackson, who had over 15 years of experience working with clinical trials, claimed she “repeatedly informed her superiors of poor laboratory management, patient safety concerns and data integrity issues.”

She also gave The BMJ a cache of internal company documents, photos and recordings highlighting alleged wrongdoing by Ventavia.

“Her job was to fix things. They wouldn’t fix them. She reported it to the FDA, and six hours later was fired from her job,” Mendenhall said.

He added:

“There was not informed consent. They were making up records. I mean, it was just endless. They were violating patient privacy, which is critical in a clinical trial because you have to not know who’s getting the shot in order to determine any effectiveness.

“Basically, the allegations that she brought forward show that the clinical trial that she saw, what she saw of it, was essentially worthless. It wasn’t valuable or useful data.”

Jackson filed her qui tam lawsuit under the FCA in January 2021. A qui tam action refers to any legal case where a private citizen initiates legal action on behalf of a state.

Documents released in November 2021 supported Jackson’s claims that she was directly involved in the Phase 3 trials for the Pfizer-BioNTech COVID-19 vaccine.

‘Level of ignorance’ of scientific facts by government officials ‘astounding’

In February 2022, the federal government declined to intervene in the lawsuit on Jackson’s behalf but reserved the right to intervene at a later date.

Later that month, Jackson filed her first amended complaint, while the court unsealed 400 pages of exhibits.

In July 2022, Pfizer asked the court to dismiss Jackson’s lawsuit on the basis that the U.S. government was aware of wrongdoings in the clinical trials but continued to do business with the vaccine maker. In March 2023, Truncale granted the motion to dismiss, ruling that Jackson had not proved the companies violated the FCA.

Jackson appealed the dismissal in April 2023, and in August 2023 submitted a motion to file a second amended complaint, which was granted in September. Jackson filed her second amended complaint in October 2023.

Pfizer and Ventavia filed motions to dismiss the second amended complaint later in October 2023, while the U.S. government filed its motion to intervene and dismiss in March 2024. Oral arguments discussing the motions to dismiss took place on May 1.

“What happened in the interim here while we’re fighting the case and moving forward, apparently the government itself decided that what we were doing in exposing Pfizer and Ventavia and ICON, the three companies involved here, was contrary to the public health policy in the United States,” Mendenhall said.

In ruling in favor of the government, the court cited a 2023 U.S. Supreme Court decision that gave the government significant leeway concerning when it could intervene in an FCA case and on what basis.

According to Mendenhall, this occurred despite meetings Jackson and her legal team had last year with representatives of the U.S. Department of Justice (DOJ), during which he said they “were completely unaware” of evidence questioning the safety of the COVID shots, including SV40 DNA contamination and vaccine injuries.

Mendenhall said:

“The level of ignorance about the scientific facts that we have uncovered was astounding to me, for someone who is supposed to be in charge of a major decision on behalf of the United States’ people, whether these shots need to be pulled from the market, whether Pfizer needs to be prosecuted or at least held civilly liable along with the other companies.

“I think that, certainly for some in the government, they just don’t want to face what they’ve actually done … they have hurt, damaged the health of millions of Americans and tens of millions, at least, around the world.”

According to Mendenhall, government attorneys were “actually sitting on the side of the courtroom with Pfizer” attorneys during the May 1 hearing.

“How strange that was to have the defendants sitting with the government who’s supposed to be going after them,” Mendenhall said.

In April, Pfizer submitted a statement to the court in support of the U.S. government’s motion to intervene and dismiss.

Pfizer previously was fined in connection with the FCA. As part of a 2009 settlement, the company paid $2.3 billion in fines — the largest healthcare fraud settlement in the history of the DOJ — stemming from allegations of illegal marketing of off-label products not approved by the FDA.

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.

August 16, 2024 Posted by | Deception, Science and Pseudo-Science | , , , | Leave a comment

Court Denies Jordan Peterson’s Appeal as Free Speech Fight Heats Up in Canada

By Didi Rankovic | Reclaim The Net | August 15, 2024

Psychologist and author Jordan Peterson has announced that Canada’s Supreme Court refused his appeal against undergoing social media re-education (“remedial”) training.

The case stems from the demand of the Ontario College of Psychologists (which licenses practicing clinical psychologists) for Peterson to be subjected to media training. The ruling now means he is to pay court costs to the organization seeking to impose this measure on him.

According to Peterson, the demand was spurred by his negative stance regarding what’s known as “gender-affirming care,” the doomsday climate change narrative (that he spoke about on Joe Rogan’s podcast), and criticism of Canadian Prime Minister Justin Trudeau.

In a video posted on YouTube, Peterson said the court’s “terrible decision” not to consider his appeal was yet another “blow to free speech” in his country – and could well result in the revoking of his license to practice, while the ultimate goal of the social media re-education would be to get “something approximating a public apology” for his opinions and for expressing them.

Peterson previously mentioned his criticism of social service workers and police “threatening to apprehend the children of the Trucker Convoy protestors” as another reason for the Ontario College of Psychologists wanting to get him “reeducated” – though he did not speak about this in the YouTube video.

In a post on X, Peterson said that the Supreme Court ruling amounted to admitting that “mid-level bureaucrats who rule the professional colleges and regulatory boards” have more power than the Canadian Charter of Rights and Freedoms.

In another post, he criticized Ontario Premier Doug Ford’s government which he said was “overseeing the commissars” standing in the way of conservatives’ free expression, including “perhaps” Ford himself.

Peterson is also critical of the way Canada’s CBC covers the case (including his remarks on the Rogan podcast), referring to the broadcaster as “paid lackeys.”

But Peterson has received support from other corners, including Alliance Defending Freedom (ADF) International, who said they were willing to work with him “to see if he wants to take the case international” – which he seems to be open to.

And Canadian Conservative Party leader Pierre Poilievre lambasted the decision as an attempt to impose forced political reeducation, noting that this came after “another government bureaucracy threatened to ban a Canadian from practicing his profession because he expressed political opinions the state doesn’t like.”

August 15, 2024 Posted by | Civil Liberties, Full Spectrum Dominance, Mainstream Media, Warmongering, Science and Pseudo-Science | , | Leave a comment

How Antidepressants Are Numbing More Than Depression

The devastating effects on empathy, love, intimacy & sex

By Dr. Roger McFillin | Radically Genuine | August 15, 2024

In our relentless pursuit to transcend the human suffering, we’ve stumbled into a dangerous oversimplification: an improved mental state reflects the absence or decrease in negative emotional states. This reductionist view has not only cheapened our understanding of the human emotional spectrum but has also paved the way for a troubling linguistic shift.

The word “sad” has all but vanished from our lexicon, replaced by the catch-all term “depression” – a linguistic sleight of hand that medicalizes every shade of human sorrow, from loneliness to anxiety, from fear to disappointment. This semantic broadening has opened the floodgates for indiscriminate prescribing of “antidepressant” drugs, extending far beyond their original purpose to treat clinical depression.

Today, these powerful drugs are doled out for an alarming array of off-label conditions: gastrointestinal issues, fibromyalgia, grief, chronic pain, and eating disorders, to name but a few. This prescription epidemic is built not on scientific evidence, but on a dangerous myth – the allure of a quick fix for life’s complexities. The medical profession and mental health communities, seemingly hypnotized by the promise of “antidepressant” effects, have unwittingly become complicit in a grand experiment on human neurochemistry.

At the heart of this phenomenon lies a disturbing paradox: the very mechanism that gives these drugs their “antidepressant” label – emotional blunting – is causing more harm than good. By dampening our ability to feel, these “medications” offer a Faustian bargain: potential short-term relief from suffering at the cost of our full range of human experiences.

For those battling severe clinical depression, the trade-off of emotional blunting might seem a necessary evil. Yet paradoxically, these individuals often struggle most acutely with the very emptiness that antidepressants can exacerbate. More alarmingly, the vast majority caught up in the widening net of antidepressant prescriptions aren’t facing such severe depressive episodes. For them, the potential for permanent emotional deadening was never a consideration, let alone a risk they knowingly accepted.

Emotional Blunting is Not Mental Healthcare

In our misguided quest to eradicate pain, we’ve stumbled upon a chemical lobotomy that threatens the very essence of what makes us human. Emotional blunting, the insidious “side effect of antidepressants”, doesn’t just dull our sorrows – it extinguishes the vibrant flames of joy, love, and connection that give life its meaning.

Imagine a world painted in shades of gray, where the highs of ecstasy and the lows of despair are replaced by a monotonous, tepid middle ground. This is the reality for countless individuals trapped in the purgatory of SSRI-induced emotional blunting. They walk through life as spectators, unable to fully participate in the rich tapestry of human experience.

The medical establishment, in its haste to silence the symptoms, has forgotten a fundamental truth: pain, in all its forms, is not just an inconvenience to be eliminated. It’s a vital signal, a call to action, a catalyst for growth and change. By indiscriminately muting this signal, we’re not just treating depression – we’re risking the very essence of what makes us human.

But the consequences of this chemical flattening extend far beyond personal discomfort. Recent research has unveiled a chilling truth: SSRIs decrease affective empathy, our ability to emotionally resonate with others’ experiences. Neuroimaging reveals a reduction in activity across three crucial brain regions associated with empathy for pain. In our attempt to shield ourselves from suffering, we’ve created a generation of emotional zombies, incapable of truly connecting with the joys and sorrows of those around them.

Consider the implications for love and attachment – the very foundations of human society. How can one form deep, meaningful bonds when the heart’s strings have been chemically severed? The butterflies of new love, the warmth of familial affection, the bittersweet ache of nostalgia – all reduced to mere concepts, intellectually understood but never truly felt. In this emotional wasteland, how can we expect individuals to develop a robust sense of gender and sexual identity, both of which are intimately tied to our capacity for emotional and physical intimacy?

The cruel irony is that in our desperate bid to numb pain, we’ve numbed everything that makes life worth living. Joy becomes a faded memory, a concept understood but no longer experienced. The exhilaration of achievement, the quiet satisfaction of a beautiful sunset, the overwhelming surge of love for a newborn child – all diluted into pale imitations of their former glory.

This emotional castration strikes at the very heart of the human spirit. Our ability to feel deeply – to be moved by music, stirred by art, inspired by acts of kindness – is what separates us from machines. It’s the wellspring of creativity, the driving force behind innovation, the fuel for compassion and altruism. By chemically muting these essential aspects of our humanity, we risk creating a society of hollow individuals, going through the motions of life without ever truly living.

The consequences ripple out far beyond the individual. A populace incapable of deep emotional resonance is a populace ripe for manipulation, apathy, and moral decay. How can we expect people to fight injustice, to stand up for the oppressed, to sacrifice for the greater good, when they can no longer feel the burning indignation or overwhelming compassion that drives such actions?

In our shortsighted attempt to eliminate suffering, we’ve stumbled upon a cure far worse than the disease. The price of emotional blunting is nothing less than our humanity itself. As we continue down this perilous path, we must ask ourselves: in our quest for painlessness, are we willing to sacrifice everything that makes us human? What impact does this emotional blunting have on sexual desire and intimacy?

Post SSRI Sexual Dysfunction (PSSD)

Imagine a world where the very essence of your being – your capacity for intimacy, pleasure, and connection – is suddenly and inexplicably stripped away. This isn’t the plot of a dystopian novel; it’s the harsh reality for countless individuals suffering with Post-SSRI Sexual Dysfunction (PSSD), a hidden epidemic born from our society’s pill-popping approach to mental health.

A vibrant libido isn’t just about carnal pleasure; it’s the body’s barometer of vitality, a complex symphony of physical, hormonal, and psychological factors humming in harmony. But for those struck by PSSD, this life-affirming melody is replaced by a deafening silence.

PSSD is the pharmaceutical industry’s dirty little secret, a Pandora’s box of sexual side effects that persist long after the last antidepressant pill is swallowed. We’re talking about a cruel trifecta of desire destroyed, genitals numbed, and an inability to orgasm.

The numbers are staggering – up to 73% of patients dancing with these serotonin-enhancing devils report one or more of these bedroom-killing effects. That’s not a side effect; that’s a full-blown assault on human sexuality.

But here’s where it gets truly Kafkaesque: PSSD doesn’t play by the rules. It doesn’t fade away when you kick the meds to the curb. No, it sets up shop in your nervous system, potentially rewiring your sexual circuitry for years – or even indefinitely. Imagine trying to rebuild your life post-depression, only to find that your capacity for one of life’s most fundamental joys has been carpet-bombed into oblivion.

The medical community, in its infinite wisdom, largely turns a blind eye to this sexual holocaust. PSSD sufferers are left adrift in a sea of misdiagnoses and dismissals, their anguish compounded by the very professionals sworn to help them.

As for the root cause of this sexual sabotage? The jury’s still out. Some point to a chemical lobotomy of the brain’s pleasure centers, others to a genetic vandalism that silences the body’s sexual whispers. But while the white coats scratch their heads, real people are left struggling with shattered relationships, crippled self-esteem, and a quality of life that’s been gutted like a fish.

We stand at a critical juncture in mental health care, facing a silent epidemic that threatens the very essence of human experience. Post-SSRI Sexual Dysfunction (PSSD) is not just a side effect – it’s a life sentence of emotional and sexual numbness that demands immediate recognition and action.

To the medical community, pharmaceutical industry, and mental health advocates: I implore you to acknowledge PSSD as a real and devastating condition. To researchers and funding bodies: We desperately need your support to unravel the mechanisms behind PSSD and develop effective treatments. Donations could be the lifeline that restores hope to countless sufferers.

But recognition and research are not enough. We must revolutionize the informed consent process for antidepressant prescription. To every potential patient, we pose this grave question:

Would you willingly sacrifice your ability to feel emotions deeply, to experience sexual desire, and to forge intimate connections, all for the possibility of short-term relief?

This is not a hypothetical – it’s the reality faced by PSSD sufferers worldwide. We demand transparency about these risks before a single pill is prescribed. The human cost of our current approach is too high, the potential for lifelong suffering too great. It’s time to prioritize true informed consent and explore alternative treatments that don’t gamble with the core of our humanity. The stakes couldn’t be higher – it’s not just about saving lives, but preserving what makes those lives worth living.

I encourage everyone to visit the PSSD Network to learn more about this debilitating condition.

August 15, 2024 Posted by | Science and Pseudo-Science | | Leave a comment

Routine Infant Hepatitis B Vaccination Fails to Protect Into Young Adulthood

Parents Should Not Expect a Long-Term Benefit

By Peter A. McCullough, MD, MPH | Courageous Discourse™ | August 12, 2024

In 1991, the Advisory Committee on Immunization Practices (ACIP) first recommended that all infants in the United States receive the hepatitis B vaccine at birth or within 1–2 months of age. The goal was to prevent maternal transmission of the hepatitis B virus (HBV) and reduce the incidence of infections in babies. Many healthy mothers without hepatitis B or risk factors such as IV drug abuse with normal infants ask what is the benefit in their babies?

The CDC recommends that children receive three doses of the hepatitis B vaccine as part of their routine childhood vaccine schedule:

  • First dose: Within 24 hours of birth
  • Second dose: Between 1–2 months of age
  • Third dose: Between 6–18 months of age

What happens later in life when young people go into the medical field and are potentially exposed to hepatitis B in sick patients? Posuwan et al evaluated a prospective cohort of young people (mean age 18 years) going into medicine and evaluated their antibody titers as a proxy of enduring immunity to hepatitis B.

Posuwan N, Vorayingyong A, Jaroonvanichkul V, Wasitthankasem R, Wanlapakorn N, Vongpunsawad S, Poovorawan Y. Implementation of hepatitis B vaccine in high-risk young adults with waning immunity. PLoS One. 2018 Aug 20;13(8):e0202637. doi: 10.1371/journal.pone.0202637. PMID: 30125298; PMCID: PMC6101408.

The investigators were disappointed to find that only 6.9% had long-lasting immunity to hepatitis B, and thus underwent booster doses upon entering medical school. It is unclear when immunity is lost in this cohort. The results are important for parents to understand that the hepatitis B shots given at birth are only applicable if the mother has hepatitis B or serious risks for carrying it including active IV drug abuse. Otherwise the vaccine schedule for this illness has little value at that age.

August 15, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular | , | Leave a comment

Mpox Vaccine Maker’s Stock Price Soars After WHO Declares Global Public Health Emergency

By Brenda Baletti, Ph.D. | The Defender | August 15, 2024

Stock prices for mpox vaccine maker Bavarian Nordic surged after the World Health Organization (WHO) on Thursday declared mpox a global public health emergency.

The company’s share prices jumped 17% in early trading in Copenhagen today, Forbes reported, after climbing 12% yesterday when the WHO made its announcement. In the U.S., shares were up 33% this morning.

The WHO cited recent outbreaks in the Democratic Republic of Congo (DRC) and neighboring nations in its declaration.

In the first known infection of its kind outside Africa, Sweden today confirmed a case of the highly contagious strain of mpox, according to NBC News. The WHO’s European regional office in Copenhagen said it was discussing with Sweden how best to manage the newly detected case, according to Medical Xpress.

This is the second time in two years the WHO has declared mpox a “public health emergency of international concern” PHEIC — pronounced “fake” — which is its highest form of an alert.

The announcement follows a declaration Tuesday by the Africa Centres for Disease Control and Prevention that mpox is a continent-wide public health emergency.

Last week, the WHO triggered the process to grant Emergency Use Listing to two mpox vaccines, although it didn’t name which ones it would list. The agency also invited manufacturers of mpox vaccines to submit an “expression of interest” for Emergency Use Listing.

The DRC, where the outbreak is concentrated and most severe, has approved two vaccines — Japan’s LC16 and Bavarian Nordic’s Jynneos, which is also marketed as Imvamune and Imvanex.

Bavarian Nordic is one of the few companies in the world with an already-approved mpox vaccine that is also available in large quantities. Other contenders, such as Emergent BioSolutions’ ACAM2000 have been available under special investigational protocols. Others, like Tonix Pharmaceuticals, have experimental shots that are in earlier stages of development.

LC16 is a smallpox vaccine licensed in 1980 in Japan and approved in July 2022 for mpox. It isn’t commercially available, but there are large supplies in Japan’s national stockpile, the Center for Infectious Disease Research and Policy reported. Like Jynneos, it is a third-generation mpox vaccine that uses attenuated virus strains.

Jynneos and ACAM2000 can cause myocarditis, pericarditis and other serious side effects at high rates, Dr. Meryl Nass told The Defender last week, as the labels for both drugs indicate.

The Japanese LC16 vaccine also has been linked to encephalitis, Nass reported on her Substack today.

“The WHO is using the monkeypox outbreak in Africa to fast-track, under emergency use, two monkeypox vaccines,” Dr. Kat Lindley, a senior fellow at FLCCC Family Medicine and president of the Global Health Project told The Defender.

“We need to use discernment and evaluate risks and benefits before recommending any experimental new product to a vulnerable population,” she said.

The African CDC in a LinkedIn post said it needed 10 million doses to control the outbreak and called for global support for its vaccination efforts.

Bavarian Nordic’s CEO Paul Chaplin told Bloomberg the company can provide 10 million doses of its vaccine to African countries over the next year and a half.

In an interview Wednesday — before today’s stock price surge — Chaplin said, “We have inventory and we have the capabilities. What we’re missing are the orders.”

In May 2022, the WHO announced it would phase out the name “monkeypox” and rename the disease “mpox” to avoid the stigma generated by associating the disease with monkeys.

WHO process for issuing PHEIC declarations ‘non-transparent and contradictory’ 

WHO Director-General Tedros Adhanom Ghebreyesus said in his press announcement that the agency decided to declare a PHEIC because:

“The detection and rapid spread of a new clade of mpox in eastern DRC [Democratic Republic of Congo], its detection in neighboring countries that had not previously reported mpox, and the potential for further spread within Africa and beyond is very worrying.”

The WHO declaration signals a public health risk requiring an international coordinated response. It can lead to WHO member countries and private investors pouring substantial resources into countries with outbreaks to facilitate sharing of vaccines, treatments and testing.

The declaration also grants the WHO authority to issue travel warnings or restrictions, to review and critique the validity of public health measures by member countries and to help persuade people that they ought to follow public health recommendations.

This is the eighth public health emergency the WHO has declared since 2007, when it substantially revised its International Health Regulations (IHR). Critics have called the process for designating such an emergency “non-transparent and contradictory.”

In July 2022, the WHO declared mpox a global emergency after reporting the disease had spread to more than 70 countries, mostly affecting gay and bisexual men. At the time, Tedros made the declaration unilaterally, in direct contradiction to independent review panel advice.

At that time, the Jynneos vaccine was licensed in the U.S. and ACAM2000 was “made available for use against mpox in the current outbreak [2022] under an Expanded Access Investigational New Drug (EA-IND) protocol.” Jynneos received emergency use authorization in the U.S. for children under 18 considered to be at high risk.

Although in the U.S. monkeypox has appeared to be a mild illness, several lucrative government contracts in 2022 paid the vaccine makers hundreds of millions to stockpile the vaccines.

The 2022 outbreak reportedly affected nearly 100,000 people, primarily gay and bisexual men, in 116 countries and about 200 people died.

Despite media hype and hundreds of millions of dollars spent to stockpile mpox vaccines in the U.S., the designation was quietly withdrawn in May 2023, “given the sustained decline in cases.”

On Aug. 8, the Biomedical Advanced Research and Development Authority renewed its contract with Bavarian Nordic, committing $156.8 million to manufacture and store Jynneos doses to partly replenish the inventory used to manufacture vaccines in response to the mpox outbreak in 2022.

Critics suggest ‘common sense mitigation measures’

Mpox was first detected in humans in 1970 in the DRC, according to the WHO, and is considered endemic to countries in central and west Africa, with the number of cases rising and falling periodically.

The disease causes flu-like symptoms and pus-filled lesions. It is usually mild but can be serious, particularly in people with weakened immune systems, Reuters reported.

In its announcement Wednesday, the WHO said the DRC is experiencing a severe outbreak of mpox, with 15,600 cases and 537 deaths. It said the current outbreak is caused by a virus strain, or “clade” — clade 1b — that is more severe than clade 2, which was responsible for the global outbreak in 2022.

It “appears to be spreading mainly through sexual networks,” and it has been detected in neighboring countries of Burundi, Kenya, Rwanda and Uganda, with 100 “laboratory-confirmed cases of clade 1b” in total in those countries.

Lindley said health officials are most likely using PCR tests, which were shown during the COVID-19 pandemic to generate false positive results.

“We really have no idea,” she said, if the alleged deaths are “complications of people who have depressed immune systems and are dying of other things.”

“Why would we start mass vaccination with a new product for which we know nothing about the safety profile when common sense mitigation measures can work?” she asked. “If it is sexually transmitted, use a condom or abstain from sex. If it can be transmitted through secretions, wash your hands and don’t touch people with clinical presentation.”

Nass expressed similar skepticism on her Substack:

“If this generally mild viral illness is killing people, what is the cause of death? Does it only cause death in severely immune suppressed patients? Are babies dying due to dehydration? Do we need to treat babies with fluids rather than give them a vaccine that was never tested in babies? Lots of unanswered questions.”

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.

August 15, 2024 Posted by | Science and Pseudo-Science | , | Leave a comment

The Academic Whistleblower

A Human Sacrifice Worth Making?

By Lisa Hutchinson | Health Advisory & Recovery Team | August 14, 2024

Recently, I listened to an interview with Dr Carl Elliott based on his published book released in June 2024 titled “The Occasional Human Sacrifice: Medical Experimentation and the Price of Saying No”. Dr Elliott is a bioethicist at the University of Minnesota who was trained in medicine as well as philosophy. For years, he fought for an independent inquiry into a case of corruption at a psychiatric research study at his own university in which sadly an especially vulnerable patient lost his life. Carl experienced first hand what it is like to be an academic whistleblower, and endured a terrible experience. His own efforts resulted in him being shunned by his friends and colleagues and impeded by his own university, who denied any wrongdoing, until an independent state investigation finally vindicated his claims after a 7-year-long battle.

Carl posits that As mentioned, his foray into this is very sad and disturbing. He detailed the extraordinary case of a mentally vulnerable man, Dan Markingson, who was admitted to a psychiatric unit after experiencing a series of psychotic episodes. Despite being a danger to himself and others, he was enrolled on a clinical trial of a new multi-drug regimen. Dan was coerced into following the treatment decisions of his psychiatrist, but against the strong objections of his concerned mother, he entered the study because he gave his “consent”. Worried for his safety, Dan’s mother spent several months trying to get him out of the study, after his behaviour dramatically worsened. She wrote to the study centre and study coordinator to ask to remove her son from the study. Despite her justified concerns, she was ignored. Tragically, several months later in the Spring of 2004, Dan killed himself in extreme circumstances.

Carl discussed several stories of how participants of medical research can be deceived into taking part in experimental programmes they do not understand, even in circumstances when the mortality risks are high. Many patients are coerced into studies with blatant financial conflicts of interest or industry funding. When Carl learned of Dan’s case and raised concerns he could not get anyone to take him seriously, so he decided to do his own research and publish a book. By bringing this issue to a broader audience, Carl hoped it would prompt the university into doing something, but this failed spectacularly, and he became a despised figure in his own academic centre.

After learning of Dan’s case in 2008, Carl spent 7 years trying to get Dan’s death investigated. His efforts included creating petitions, writing to the University Alumni, writing to the FDA and federal government. Eventually, he got a state investigation, and although the ruling was positive and vindicated everything he and other critics raised, the follow up was non-existent. His efforts accomplished very little – there was no apology from the academic university, no compensation to victims, no reform, or sanctions for the wrongdoers or efforts to learn from the devastating situation. This was a demoralising ending after such a long struggle.

Ethical standards and integrity have been gradually compromised for several decades. It is unclear why there is pressure to violate ethical rules in the medical research domain. Some of the reasons are financial, but perhaps a bigger issue is the pursuit of glory for some academic clinicians. In psychiatry, balancing the interests of individual participants in trials versus the pursuit of scientific answers is compromised. In 90% of the scandals Carl teaches about at the University of Minnesota, trial participants are mentally ill, disabled, have low socioeconomic status, are vulnerable, and cannot look out for themselves – collective traits that are exploited. As he describes it, the ‘honour code’ in medicine should safeguard and offer protections for such patient groups.

Many whistle-blower stories in the 1970s and 1980s predate the rise of the Big Pharma trials of today. Among clinicians and academics there is a race for glory, status, academic promotion, awards, and prizes. In the 1990s, the financial status changed unrecognisably with recent scandals having huge money stakes, absent from earlier corruption cases. In the past 20-30 years, academic research is less about patient care and more about research funding, which is a toxic situation. Sectors outside medicine have a regulatory system, which is absent in medical research. Instead, an ‘honour’ system exists in which professionals are trusted to behave honestly. Ultimately, there is a quasi regulatory responsibility by industry for overseeing integrity in its multi-billion dollar sector. Coupled with medical arrogance, bioethics within academic centres is now funded by the same industry players funding the studies. Thus, bioethics has been absorbed into academic health centres, relocating ethics to the belly of the beast!

There is a huge difficulty in maintaining independence and not being ‘captured’ by academic medicine. When research funding for academic salaries or tenure is through government-led institutions combined with the pressure to publish findings in high-profile medical journals, this creates a dangerous authoritarian culture. Such an environment has sometimes led to the dehumanisation of the patient, and maintaining ethical standards is a challenge. In a fee-for-service culture where high financial incentives exist, dismissing adverse effects of experimental treatments and lowering the inclusion criteria threshold are all too pervasive. There are of course well-intentioned medical professionals, but corporate overlords, dependence on practice guidelines coupled with the tremendous academic workload, stymies patient safeguarding and forges academic burnout.

What do whistleblowers have in common? They are motivated by honour, integrity, and moral concerns. They have no expectation for financial gain and they do not derive any personal advantages for themselves; in fact, they usually have everything to lose, such as financial stability and reputational damage, yet they still speak out. The reason many whistleblowers persisted in what they felt was a near futile struggle for years or even decades before resolution, was they were tenacious and refused to give up. Notably, cases known to the public are only examples in which a ‘resolution’ was achieved, even though the whistleblowers had reputational damage and no apology or financial compensation for victims was provided. So the situation is likely worse in terms of the treacherous path travelled by many whistleblowers, as we only hear of the most ‘successful’ cases.

Whistleblowers who worked for the public health sector often got nowhere. All whistleblowers had a common metaphor – if they were to look in the mirror, could they live with themselves if they did not do something? Many experience a form of PTSD and none experience improved lives following their exposure. Does disillusionment occur prior to whistleblowing, or when attempts or reports are ignored? Sadly, it seems there is a slow descent into nihilism. Most whistleblowers believe that if the outside world knew what they knew, this would encourage people to defend or change the corruption – notably this never happens. They also hope that close friends or relatives will stand by them, but in its absence, an existential break occurs.

Some whistleblowers feel a sense of guilt because of their complicity in their own industry. Others feel guilt out of a sense of disloyalty to their peers or not wanting to expose an entire institution into disrepute. The notion that whistleblowers are heroic victorious figures that embark on a ‘David versus Goliath’ image is a falsehood! Perhaps the whistleblower is a rare breed; many who are concerned might be more realistic or disillusioned to begin with, so have a lower expectation in terms of likely justice. Possible reasons there are not more whistleblowers is because they know their action would be futile, they could get disciplined, they did not want to snitch on friends or colleagues, or they had a (misplaced) loyalty to their institution. Indeed, a recent BMA survey reported that 61% of doctors polled about patient safety concerns would not raise concerns because of fears that they or their colleagues might be “unfairly blamed or suffer adverse consequences”.

Organisational loyalty is puzzling because an institution intrinsically seems to instil loyalty, but fighting something that undermines it, ironically goes against those who expose it. One way to address this would be to establish independent organisations to investigate such cases. Although many are aware bad behaviour exists, those in senior leadership positions do not ask, so the corruption remains under the radar. One example was at the Karolinska Institute over lethal synthetic trachea transplants, in which a surgeon had falsified results and misled the hospital about the health of those who received the transplants. While the surgeon involved, Paolo Macchiarini, received a prison conviction, the Swedish legal authorities and Karolinska Institute did not apologise to whistleblowers or compensate the victims. This high-profile case did not tarnish the institute’s reputation; in fact, it is rare for institutions to suffer in medical corruption cases. Leaders at academic institutions worry that if problems are exposed, it will deleteriously impact them, so silence or internal handling is considered the best policy.

One would think it would be better to come clean so that things can be remedied, and the error not repeated, in the hope wrongdoers are punished and institutions reformed. However, in his research and experience, Carl has never come across an institution that took positive resolution steps. Academic organisations still attack anyone who threatens their reputation. Often the senior figures in such scandals, such as Deans, Presidents or Directors, have left by the time a scandal is exposed, which one might think would help reduce any reputational damage. Although no one currently employed would be implicated in such scandals if the culprits have departed, the corrupt behaviour remains unchanged, so it is hard to offer an explanation.

The general public has a high opinion of doctors, believing medical professionals have strong ethics and want to help people and save lives. While this is true for many doctors, modern medicine has become big business financially. Patients are nowadays consumers, which is an inevitable slide into corruption. The marketing of medical devices and drugs has become more covert, such as  bribes given to doctors. The scandals involved to preserve the illusion of integrity internally and externally are egregious. Carl is sceptical that a greater awareness of Big Pharma and how their marketing efforts operate would result in a more-positive outcome.

Ultimately, drug representatives are salesmen: they try to get doctors to prescribe their drugs. For many years, the vast majority of marketing was aimed at doctors not patients, although direct-to-consumer advertising is now ubiquitous. Huge financial sums are at stake, and most doctors do not like to imagine their prescription decisions are influenced by Big Pharma. Drug representatives have developed relationships with doctors – they are mercenaries. In the blockbuster drug era, especially in the USA, it is possible to make billion dollar drug sales for chronic illnesses, and doctors can be exploited to earn millions. Other than consultancy, doctors can receive lavish gifts, such as expensive dinners or premium tickets to expensive events. In the 1990s, the development of script tracking enabled the ability to measure in real time how marketing efforts affected doctors script sales. All drug representatives have access to the same data, so they compete for doctors with highest prescriber practices.

Ultimately, all the systems follow the same money trail. People who run the hospitals are worse, and according to Carl, those getting most from industry have the largest bribes. This farce is omnipresent; alarmingly, many bioethicists are not averse to taking industry money, highlighting that we are falling off the bioethics cliff. It is striking how universal and commonplace the language of medicine has become to describe the human experience. People define themselves on the basis of a medical diagnosis, illustrating how marketing has infiltrated our lives. For instance, people describe medical interventions as the person they are inside and how this fulfils their authentic self. It is an illusion that an intervention helps you become who you really are on the inside. Carl suggests pressure exists either to fit in or to stand out, which are two sides of the same coin.

Does bioethics have a rescue philosophy? In general, bioethics is a huge disappointment, with the status quo unchanged since the 1980s. Bioethics has taken up residence in academic health centres and is controlled by the same corrupt forces. It is sobering that not a single medical research scandal exists, whether patient care, sexual abuse, or research misconduct, in which a bioethicist has criticized their own institution. They know how unwelcome it would be, so they keep quiet! The conclusions of Carl’s book and interview are disheartening: being a whistleblower is not worth the hassle or personal devastation involved for the noble individuals who speak out. Since the Covid era, whistleblowers have become more prolific as many no longer accept the associated injustice. Let’s hope this seeds change and a much-needed new cultural shift to inspire and support future academic whistleblowers rather than deter them. The brave but solitary path of the academic whistleblower must be a human sacrifice worth taking!

August 15, 2024 Posted by | Book Review, Corruption, Science and Pseudo-Science, Timeless or most popular | | Leave a comment

Big Pharma Funds COVID Fact Checkers

By Brenda Baletti, Ph.D. | The Defender | August 9, 2024

FactCheck.org, the organization that flags “misleading” COVID-19 content for Facebook, is supported by the Robert Wood Johnson Foundation, a philanthropic organization funded by pharmaceutical giant and vaccine maker Johnson & Johnson (J&J), YouTube commentator Jimmy Dore reported.

Dore said his own shows have often been slapped with a “misleading” label when he covered issues related to COVID-19 or vaccines.

“These fact check organizations aren’t there to check facts,” Dore said. “They’re there to push a political point of view and an agenda and to discredit people.”

Dore said when the organization “fact-checked” his work in the past, its claims were always “bogus.” He said FactCheck.org never reached out to consult him about his content, it twisted his words and it never even pointed to any erroneous facts.

Instead, he said, “They didn’t like my headlines,” and they would say they were misleading.

Johnson & Johnson’s viral vector COVID-19 vaccine received emergency use authorization from the U.S. Food and Drug Administration in February 2021. After the shot was linked to dangerous blood clots, its use was suspended a couple of months later and it was eventually completely pulled from the market in May 2023.

The Robert Wood Johnson Foundation was established in 1952 by Robert Wood Johnson II, who ran J&J with a bequest of shares from the pharmaceutical giant. Today, although the foundation says it has diversified its holdings, it holds nearly $2 billion in J&J stock.

Its current CEO, Dr. Richard Besser, formerly worked at the Centers for Disease Control and Prevention, where he was acting director during the H1N1 outbreak.

When Rep. Thomas Massie (R-Ky.) first sounded the alarm in 2021 about FactCheck.org on Twitter (now X), the organization responded by saying, “The views expressed by FactCheck.org do not necessarily reflect the views of the foundation.”

The organization continues to receive funding from Robert Wood Johnson for its work “correcting health misinformation.” It reiterates on its website, the foundation “has no control over our editorial decisions.”

“The fact checking organization,” Dore said, quoting Michael Rectenwald, Ph.D., “is in collusion with Big Pharma.”

Watch ‘The Jimmy Dore Show’ here:

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.

August 11, 2024 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular, Video | | Leave a comment