A British doctor, Aseem Malhotra, has just had a two part, peer-reviewed paper published in the Journal of Insulin Resistance. The aim of the paper was to gain a better understanding of the true benefits and potential harms of the mRNA Covid vaccines. You can read Part 1 and Part 2 in full by clicking on the links.
Dr Malhotra. a cardiologist by trade, was originally a strong Covid vaccine advocate. He volunteered in a vaccine centre, was one of the first people to be double dosed and appeared on morning television to encourage everyone to get vaccinated. He was surprised and concerned at vaccine-hesitant patients when they asked about ‘anti-vax’ propaganda.
That was until, sadly, in July 2021, his father suffered a cardiac arrest and died. His father had been the former deputy chair of the British Medical Association (BMA) and honorary vice president. The 73 year old gentleman was extremely fit and active and heart scans from a few years earlier had revealed no significant problems. Dr Malhotra was shocked to read his father’s post mortem which found that two out of three of his major arteries had severe blockages.
Aseem couldn’t explain the post mortem findings and became more concerned in November 2021 after reading a peer-reviewed abstract in Circulation Journal. In the study, the mRNA vaccine was associated with significantly increasing the risk of a coronary event within five years from 11% pre-mRNA vaccine to 25% 2-10 weeks post vaccine.
He began to question his father’s death and wondered whether the Pfizer vaccination he had received six months earlier could have contributed in some way. After six months of critically appraising the data and speaking to eminent scientists, he reluctantly concluded that, contrary to his own dogmatic beliefs, Pfizer’s vaccine was far from being as safe and effective as first thought.
Questioning the data
During his reassessment of the Covid vaccine he recalled a conversation with a cardiologist colleague who decided against vaccination due to his low personal risk and concerns about short and long term harms. His colleague was particularly alarmed that, during the trials, there had been four cardiac arrests in the vaccine group but only one in the placebo group.
Next, Dr Malhotra assessed the 95% efficacy claims. Whilst this relative risk reduction made good sales material, the true value of a treatment can only be established by looking at the absolute individual risk reduction.
This turned out to be 0.84%, in other words, in a trial of 20,000 people (10,000 in the vaccine group and 10,000 in the placebo group), 4 people in the vaccine group and 88 people in the unvaccinated group would end up testing positive for Covid. Another way to express that is that you would need to vaccinate 119 people to prevent one positive test.
This absolute risk reduction figure (0.84%) is extremely important for doctors and patients to know but how many of them were told this when they received the shot? Transparent communication of risk and benefit of any intervention is a core principle of ethical evidence-based medical practice and informed consent.
The trials did not show statistically significant reductions in serious illness or mortality and in fact there were actually more deaths (19) in the vaccine group versus the placebo group (17). Furthermore, there were only nine severe cases of Covid in the placebo group, representing 0.04%. And this was in regions specifically chosen for their high prevalence of infection.
To find protection against death, then the 119 figure above (people vaccinated to prevent one positive test) must be multiplied by the number of infections that would lead to a single death in each age group. So, Dr Malhotra calculates his rate of death from Delta was 1 in 3,000 meaning the absolute risk reduction of the vaccine protecting him from death is (1 x 3000 x 119) 1 in 357,000.
As also pointed out in a recent editorial by John Ioannidis in BMJ evidence-based medicine the inferred efficacy of the vaccine from non-randomised studies may be ‘spurious’, with bias being generated by ‘pre-existing immunity, vaccination misclassification, exposure differences, testing, disease risk factor confounding, hospital admission decision, treatment use differences and death attribution’.
What should be part of the shared decision-making informed consent discussion when any member of the public is considering taking the shot is something along these lines: Depending on your age, several hundreds or thousands of people like you would need to be injected in order to prevent one person from dying from the Delta variant of COVID-19 over a period of around three months. For the over 80s, this figure is at least 230, but it rises the younger you are, reaching at least 2600 for people in their 50s, 10 000 for those in their 40s, and 93 000 for those between 18 and 29 years. For omicron, which has been shown to be 30% – 50% less lethal, meaning significantly more people would need to be vaccinated to prevent one death. How long any protection actually lasts for is unknown; boosters are currently being recommended after as short a period as 4 months in some countries.
But how many people have had a conversation that even approaches an explanation similar to that? This is before we get into the known, unknown and as yet to be fully quantified harms.
Harms
Concerns have been raised about trial participants being limited as to the type of adverse event they could report. Furthermore, hospitalised participants were withdrawn from the trial and not reported in the final results. To make matters even worse, after two months, the FDA allowed the placebo group to be unblinded and get vaccinated, completely removing any control group with which to assess adverse events.
Dr Malhotra sticks with his field of expertise, cardiology and discusses one of the most common vaccine-induced harms, myocarditis. Whilst authorities say that myocarditis is more likely after infection than vaccination, other studies have shown the opposite. There is no evidence of myocarditis until vaccination began in 2021, a full year after millions of youngsters naturally caught Covid.
Although vaccine-induced myocarditis is not often fatal in young adults, MRI scans reveal that, of the ones admitted to hospital, approximately 80% have some degree of myocardial damage. It is like suffering a small heart attack and sustaining some – likely permanent – heart muscle injury. It is uncertain how this will play out in the longer-term, including if, and to what degree, it will increase the risk of poor quality of life or potentially more serious heart rhythm disturbances in the future.
The UK’s Yellow Card reporting system is addressed and determined to be far from adequate to cope with a rapid roll out of a brand new product. 9.7 million doses were administered before the clotting problems with AstraZeneca were detected. In Denmark, they detected the problem after only 150,000 doses.
Since the beginning of the vaccine roll-out, there have been almost 500,000 adverse events reported involving over 150,000 individuals. This shows around 1 in 120 suffer an adverse event that is beyond mild. This number is unprecedented and represents the same as the total number of reports received in the first 40 years of the Yellow Card system being active. The MMR vaccine reports around 1 in 4000 suffer an adverse event.
The paper also looks at VAERS in the US which has recorded over 24,000 deaths, 29% occurring within 48 hours of vaccination and 50% within two weeks. Before 2020 there were approximately 300 deaths recorded per year.
Of most concern is that these reporting systems are actually likely to be underestimates with one paper suggesting that only 1% of serious adverse events are ever reported to the FDA. Another analysis estimated that only 10% of serious adverse events were ever reported on the Yellow Card system.
Moreover, these reporting systems will generally miss medium and long term harms as it is more difficult to attribute to vaccination.
According to ambulance service data, in 2021 there were an extra 20,000 (20% increase) cardiac arrest calls compared to 2019 and 14,000 more than 2020 in the UK.
Similarly, a recent paper in Nature revealed a 25% increase in both acute coronary syndrome and cardiac arrest calls in the 16- to 39-year-old age groups significantly associated with administration with the first and second doses of the mRNA vaccines but no association with COVID-19 infection.
More harm than good?
One has to raise the possibility that the excess cardiac arrests and continuing pressures on hospitals in 2021/2022 from non-COVID-19 admissions may all be signalling a non-COVID-19 health crisis exacerbated by interventions, which would of course also include lockdowns and/or vaccines.
Given these observations, and reappraisal of the randomised controlled trial data of mRNA products, it seems difficult to argue that the vaccine roll-out has been net beneficial in all age groups.
Dr Malhotra concludes the first part by saying that whilst risks from vaccination remain constant, the benefits reduce over time as the virus become less virulent and variants are not targeted by outdated products. He recommends a pause and reappraisal of vaccination policies.
Pandemic of misinformation
In part 2, Dr Malhotra explores the pandemic of misinformed doctors and a misinformed and unwittingly harmed public.
According to one senior doctor in regular contact with England’s Chief Medical Officer, Chris Whitty, most of his colleagues in leadership positions influencing health policy may not have been critically appraising the evidence and were instead relying on media stories on COVID-19 and the vaccines.
He says there are four key drivers and seven sins that are the root of medical misinformation:
Driver
Much published medical research is not reliable or is of uncertain reliability, offers no benefit to patients or is not useful for decision makers;
Most healthcare professionals are not aware of this problem;
Even if they are aware of this problem, most healthcare professionals lack the skills necessary to evaluate the reliability and usefulness of medical evidence; and
Patients and families frequently lack relevant, accurate medical evidence and skilled guidance at the time of medical decision making
Sins
Biased funding of research (that’s research that’s funded because it’s likely to be profitable, not beneficial for patients)
Biased reporting in medical journals
Biased reporting in the media
Biased patient pamphlets
Commercial conflicts of interest
Defensive medicine
An inability of doctors to understand and communicate health statistics.
There are six components essential to informed decision making: (1) description of the nature of the decision; (2) discussion of alternatives; (3) discussion of risks and benefits (in absolute terms); (4) discussion of related uncertainties; (5) assessment of the patient’s understanding; and (6) elicitation of the patient’s preference.
If the administration of the vaccine did not adhere to these principles (which is likely widespread, consistent with historical evidence), then it is also a significant breach of General Medical Council duties of a doctor to ‘give patients the information they want or need in a way that they can understand’.
The paper continues to look at institutional corruption and erosion of public trust, the failure of regulation, biased reporting in the media and censorship of legitimate scientific debate.
A hard hitting, yet sensible paper which should be read by everyone, especially doctors who lost their critical thinking skills over the last few years. Dr Malhotra is a regular on TV so will this be reported in the MSM… I doubt it.
During an appearance at the “Goalkeepers 2022” event, investor and philanthropist Bill Gates lamented “misinformation” that was shared about him amid the coronavirus pandemic and complained that so-called misinformation about masks and vaccines reduced compliance with mandates.
“I’d say the biggest tragedy is that it [misinformation] fragmented society where certain sources, if they told you to wear a mask, that was the last thing you were going to do,” Gates said. “Or if they told you, you know, get the vaccine, particularly to protect, reduce transmission to elderly people, they didn’t comply. It is a phenomena that held us back and hurt us in a pretty dramatic way.”
Gates also dismissed “conspiracy theories” about him wanting to track people.
“This whole tracking thing, why would I want to track you?” Gates said. “I don’t know, you know. Do I have time to track all these people?”
While Gates was seemingly referring to vaccines, just one day later, at the “Forbes 400 Philanthropy Summit,” Gates admitted that he has a group dedicated to tracking what people say about him online.
“I have a group that tracks what’s on the web that’s talking about things that connect to me,” Gates said. “Overwhelmingly during the pandemic, 95% was all the conspiracy theory stuff. It is calming down now.”
At the Goalkeepers 2022 event, Gates also complained that conspiracy theories are “cynical” and look for “one bad person who’s doing all this stuff” and welcomed “trusted sources” and “fact-checkers” partnering with social media companies to slow down the spread of content that he deems to be misinformation.
Gates’ nonprofit, The Bill and Melinda Gates Foundation, has provided hundreds of millions of dollars in funding to some of the Facebook fact-checkers whose content is used in warning labels that are appended to Facebook posts. When these warning labels are added to Facebook posts, their click-through rates decline by around 95%.
While Gates framed the debate around so-called misinformation and conspiracy theories as a tragedy that reduced compliance with the advice being pushed by trusted sources, he failed to mention that these so-called trusted sources have issued false or conflicting advice throughout the pandemic.
The theory that the coronavirus leaked from a Wuhan lab was initially dismissed as a conspiracy before so-called trusted sources finally admitted the lab leak theory was a possibility.
Those who challenged or questioned the “trusted sources” were accused of spreading misinformation and censored by Big Tech platforms, even though many of their challenges and questions later turned out to be true.
The battle with Big Tech for free speech is heating up! States are passing bills to stop the social media censorship, and legislators are holding investigative hearings, while a recent lawsuit including several State Attorneys General is making headway.
Suddenly, Biden announces the pandemic is over as the narrative is now collapsing from all sides. From boosters to kids shots, the vaccine push is faltering as lawsuits pile up to remove the last covid restrictions.
Last week, The Epoch Times reported that Dr. Rochelle Walensky, director of the Centers for Disease Control and Prevention (CDC), admitted the CDC had stopped monitoring the safety of mRNA COVID-19 vaccines using a method of analysis called proportional reporting ratio (PRR).
Walensky promised to resume the monitoring.
What The Epoch Times missed is that PRR is a fraudulent measure of vaccine harm, designed by the CDC expressly for the new COVID-19 vaccines to disguise the devastation the vaccines are causing.
Why? Because PRR measures the pattern of different vaccine side effects, but it is indifferent to the number of people reporting those side effects.
If some completely new vaccine side effect appears with the introduction of a new vaccine, PRR will catch that.
But the COVID-19 vaccines are associated with huge numbers of people reporting side effects on an unprecedented scale — and, by design, PRR misses this completely.
For example, if one person in a million dies from vaccine A and one person in a thousand dies from vaccine B, then vaccines A and B can have exactly the same PRR score!
PRR is a single number that compares the variety of different side effects for a new vaccine to the variety of side effects from past vaccines.
Of course, there have been many vaccines with different side-effect profiles in the past, and it is difficult to stand out among such a diversity of profiles.
Where the new mRNA vaccines do stand out is the unprecedented number of bad outcomes, including deaths, reported to the Vaccine Adverse Event Reporting System (VAERS).
Of all the reports in the 30-year history of VAERS, two-thirds of them were from the COVID-19 vaccines, introduced in the U.S. in December 2020.
This includes three-fourths of all deaths reported to VAERS and three-fourths of all hospitalizations.
Since the introduction of the COVID-19 vaccines, reports to VAERS have skyrocketed off the charts.
Credit: OpenVAERS
These numbers represent only the reports VAERS has processed and posted. Jessica Rose, Ph.D., has reported that VAERS is months behind in posting these reports because its staff has not increased, while its workload is roughly 50 times greater since the rollout of the COVID-19 vaccines.
The sheer volume of VAERS reports, including deaths, should have set off alarm bells within weeks after the vaccines were introduced.
Reporting only PRR and not the actual count provided a convenient cover for “business as usual.”
I am grateful to Mathew Crawford for pointing this out in an article last year.
Josh Mitteldorf, Ph.D., has a background in theoretical physics. Since the 1990s, he is best known for his contributions to the biology of aging, including many articles and two books.
A short collection of key pieces of evidence showing the COVID vaccines are not “safe and effective.” Not even close. They are the most deadly vaccines we’ve ever produced.
Executive summary
Here’s a high level collection of some of the most compelling pieces of evidence I’ve seen to date. This is not an exhaustive list, but just the key pieces of data that are impossible to explain if the vaccines are safe and effective.
I’ve divided the collection into sections and I’ve tried to limit each section to the most compelling data points. So don’t be disappointed if your favorite item isn’t mentioned in this article; I wanted to keep it short enough to be read..
The Pfizer trial 6 month report showed absolutely no all-cause morbidity or mortality benefit. There were no all-cause benefits at all. It was all negative. Ask your doctor why you should take a new, unproven medical intervention that is not shown to have an overall benefit. Even if there was a benefit of fewer COVID infections (which is seriously suspect due to the gaming below), the fact that the total all-cause numbers for both mortality and morbidity were negative means the intervention should not be recommended by any doctor.
The Pfizer trial 6 month report showed that more people died (and were injured) who got the drug than who got the placebo. In other words, the cure was worse than the disease. The drug maker claimed that none of the people in the vaccine group were killed by the vaccine. They do not reveal the tests they did and explain how they were able to make that assessment. Why the secrecy here, especially in light of the study by Bhakdi and Burkhardt showing that trained medical examiners missed the causality link in 93% of the cases they looked at? The Pfizer vaccine had 4X as many cardiac arrests in the treatment group than the placebo (see page 12 of the Supplemental Appendix). This lines up very well with the numerous cardiac-related problems related to the vaccine as documented in the study by Retsef Levi and in the VAERS data which showed that the “cardiac arrest” reports were elevated by a factor of 93X higher than the annual baseline rate (VAERS reports from all vaccines combined in previous years). For some reason, the CDC wasn’t able to detect that signal (it was only 100 times higher than normal so they ignored it for some reason; they won’t let me ask them about it). In short, the claims from the manufacturer that none of the deaths were caused by the vaccine are highly suspect since all the evidence for those claims remains hidden from public view for some reason.
The Pfizer trial 6 month report showed that at best, the drug saved only 1 COVID life per 22,000 recipients. This means that at best, after vaccinating 220M Americans, we might save 10,000 lives from COVID. But the VAERS reports show an excess death toll of well over 10,000 people and that’s before applying the minimum estimated under-reporting factor of 41. So there isn’t a mortality benefit: it’s actually the reverse. Furthermore, VAERS reports will likely only be filed for deaths in temporal proximity to the shot and is highly unlikely to report those deaths happening 5 months after the shot which appear to be the bulk of the deaths. This makes the comparison even worse. In short, we aren’t anywhere close to saving any lives at all.
The Classen paper analyzed the clinical trial data for all three US vaccines and confirmed the lack of any overall benefit. There was an increase in morbidity which was highly statistically significant in all three vaccines. It concluded, “Based on this data it is all but a certainty that mass COVID-19 immunization is hurting the health of the population in general. Scientific principles dictate that the mass immunization with COVID-19 vaccines must be halted immediately because we face a looming vaccine induced public health catastrophe.” This is exactly right.
Serious adverse reactions, including paralysis, were not reported to the FDA and there were other very serious discrepancies in the trials. For some reason, nobody seems to be interested in exploring or explaining these very serious issues. Some are very clear cut such as the case of Maddie de Garay who was one of 1,000 kids in the clinical trial. She’s paralyzed now and has to eat with a feeding tube. The FDA and Pfizer never investigated, but reported her results as mild abdominal pain in the trial results. This is fraud. Also, there were 5 times as many exclusions in the treatment arm as in the placebo arm of the trial: 311 vs. 60. Do the p-value computation on that one and you’ll find that it could not possibly have happened by chance (1e-40). It means the trial was not blinded. Why didn’t anyone in the medical community ever point this out? Nobody will tell me.
The VAERS data, which is the official adverse event reporting system used by the US government, shows that an estimated hundreds of thousands have died and millions have been injured. If these weren’t caused by the vaccine, what caused them? Why are there more adverse events reported for these vaccines than for all other vaccines in history combined? Nobody can answer that question. See this tutorial and this recent confirmation and this article on VAERS and causality. Here’s how these numbers were calculated. Here is independent confirmation of the estimates by Dr. Naomi Wolf who used different datasets. No fact checker was interested in contacting me to challenge the facts since I always insist on recording any calls. Also, the causality of events was confirmed by the Israeli safety studies, but nobody wants to look at those.Can you spot the unsafe vaccine? People at the CDC don’t see any problem with this mortality chart: all the vaccines look perfectly safe.
US disability rose dramatically soon after the vaccines rolled out (Y axis is Z-score). A 3 sigma increase is hard to explain.
As of Sep 2, 2022, the vaccination rate in Israel is now just 2.4%. They used to be one of the world’s most vaccinated countries. Today, very few people in Israel are considered to be vaccinated. If the vaccines are so beneficial, why has nearly the entire country shifted from extremely pro-vax to extremely anti-vax in such a short period of time?
Independent expert reports solicited by government officials
The Israeli vaccine safety data showed very clearly the side-effects are serious, long-lasting, and caused by the vaccines. Secondly, it showed that the Israeli authorities and the worldwide mainstream media are covering it all up. It also showed that US officials were not interested in seeing credible COVID vaccine safety that didn’t go along with the narrative. I tried to find out why, but nobody would talk to me. Harvard Professor Martin Kulldorff, a widely respected authority on vaccines, when asked why these people wouldn’t want to see the data, replied, “I don’t know.” This is the single most damaging report in the history of the COVID vaccines. Nobody wants to talk about it. They are hoping it will die. It won’t. Some people claim Israeli used a broad mix of vaccines, but that’s not true. Over 90% of the reports are from Pfizer, the bulk of the others are from Moderna. See also Israeli Investigators Find COVID-19 Vaccines Cause Side Effects: Leaked Video.
The Canadian report prepared for the Liberal Party of Canada (Trudeau’s party) showed no benefit for infection, hospitalization, and death for those under 60. “The empirical evidence investigated in this report from PHO and PHAC does not support continuing mass vaccination programs, mandates, passports and travel bans for all age groups.” You can’t have a vaccine that doesn’t work in Canada work in other countries. The authors of the report had to hide their identities for fear of retribution. The statistics analyzed were those from Ontario which is not a small province (15M people). Naturally, the mainstream press ignored the report. Nobody has shown where the experts who wrote this made a mistake. The conclusion of the report is supported by independent analysis done by Mathew Crawford of the data from San Diego County, San Diego County Data Busts a Hole in Vaccine Efficacy Narrative. So apparently, the results are not limited to Ontario.
Pre-prints from highly credible sources
The Harvard-Hopkins-UCSF study showed it is unethical to mandate vaccination for college students and anyone younger. The study clearly said, “University booster mandates are unethical.”
The Thailand study did blood tests before vs. after the jab and determined that nearly 30% of young adults experienced cardiovascular injuries after the jab. How is that safe? And why didn’t anyone in the US ever do such a study? Do we not want to know? This was a simple blood test before and after the vaccine. Why did they not notify parents as soon as the study was published?
Papers published in peer-reviewed medical journals
The Fraiman-Doshi paper looked at serious adverse event rates and found that the vaccines may not be as safe as has been claimed, but they cannot do a proper analysis because they are not allowed to see the data. “Full transparency of the COVID-19 vaccine clinical trial data is needed to properly evaluate these questions. Unfortunately, as we approach 2 years after release of COVID-19 vaccines, participant level data remain inaccessible.” You have to wonder: if the vaccine is so safe, why are the drug companies hiding the data?
The Levi cardiac arrest rate elevation paper showed a troubling correlation between vaccine doses and increased cardiac events from January–May 2021. When they tried to get data after May 2021, they were refused access. This begs the question: if the vaccines are perfectly safe, what are they trying to hide?
Articles by respected vaccine experts interpreting the data
Are the Covid mRNA Vaccines Safe? was written by Harvard professor Martin Kulldorff who until recently was on vaccine committees of the FDA and CDC. He concluded:
Fraiman and colleagues have produced the best evidence yet regarding the overall safety of the mRNA vaccines. The results are concerning. It is the responsibility of the manufacturers and FDA to ensure that benefits outweigh harms. They have failed to do so.
There are specialized tests required to diagnose a death from the COVID vaccine.
The CDC has never told any medical examiner in the US about these tests.
So the medical examiners aren’t implicating the vaccine in any of the deaths.
The question is we know what the tests are, we know there is solid evidence from multiple countries that the vaccine causes death, yet we refuse to even consider the possibility that the vaccine caused the deaths. Why?
Retracted papers published in peer-reviewed journals
The publisher hasn’t fixed the problem in over a year despite assurances it would be quickly resolved.
Here is another retracted paper that was correct:
Why are we vaccinating children against COVID-19? by Ron Kostoff
“Compared with the 28,000 deaths the CDC stated were due to COVID-19 and not associated morbidities for the 65+ age range, the inoculation-based deaths are an order-of-magnitude greater than the COVID-19 deaths!”
That is basically what I found: the vaccines kill >10X more people than the number of COVID deaths that they save. The paper passed peer review and was published. The editor of the journal quit after he was overridden by the publisher on the retraction.
The reason cited for the retraction:
The use of key terminology, specifically the key terms “inoculation” and “vaccination” diverges from common use and are incorrect, indicating clear evidence of bias.
Publicly available data from the United States Center for Disease Control (U.S. CDC) were concluded by the external reviewers to be misinterpreted to make the erroneous conclusion that the vast majority of reported deaths due to COVID-19 are actually due to other comorbidities. Such an egregious misinterpretation and misrepresentation are unacceptable.
This is completely bogus for two reasons:
The editor could have easily normalized the terminology to eliminate any perceived “bias.” They simply ask the author to do a quick search and replace.
The vast majority of COVID-19 deaths were in fact due to other comorbidities. For example, the New Mexico death records where COVID-19 was listed as the cause of death and 5 out 6 were not consistent with a COVID death. If anyone wants to challenge me on that, I have access to the death data. In Massachusetts, only 10% to 20% of the deaths listed as COVID were actually caused by COVID. Most people don’t have access to the death data, but I do. So I wonder if the journal is interested in fixing their error?
Hard-to-explain anecdotes
Can anyone explain how these anecdotes are possible?
Why don’t Dr. Paul Offit (FDA vaccine outside committee) and Professor Grace Lee (Chair, CDC vaccine outside committee) want to see the Israeli safety data? They are deliberately avoiding answering the question. Why?
Why is it illegal to analyze the vaccine vials? Why hasn’t a single medical institution done an analysis of the content of the vaccines to see if there are placebos with saline solution and the amount of mRNA degradation, rendering the vaccines useless? Why the secrecy here? If we knew what was in the vaccines would this cause harm? How?
Why are prominent people risking their careers to obtain fake vaccine cards? We know top people at Mass General Hospital have fake vaccine cards. We’ve heard that people at the highest levels of the DoD can get fake vaccine cards. It is well known that the CEO of a large pharmaceutical company bought a fake vaccine card. Why would he risk spending years in jail if the vaccines are perfectly safe?
The Died Suddenly group on Facebook was adding users at 20,000 per day making it the fastest growing group in Facebook history. They had to throttle the growth rate due to attempts by the British military to infiltrate the group to cause it to be shut down.
The average age of the people reported dead in the Died Suddenly group has been trending younger and younger over time. How can you explain that? The only worldwide massive intervention that goes to younger people is the COVID vaccine.
My neurologist stats: 11 years without needing to do a single VAERS report; this year, she needs to file 1,000 VAERS reports on 20,000 patients in the practice. How can anyone explain that if the vaccine is perfectly safe with mild, short term effects? This is similar to the 4.5% rate of neurological injury reported earlier by the Israeli Ministry of Health.
The polling results using third party polling firms (so not my followers) consistently show that more people died from the vaccine than from the virus. The mainstream media refuses to do similar surveys and most survey firms refuse to even ask the questions.
The fact that Paul Offit isn’t going to get the latest booster even though the CDC says he should. Why should any of us take the shot if Paul Offit is refusing to take the shot? He’s arguably the world’s most respected authority on vaccines and sits on the FDA outside advisory committee?
Google searches show people became interested in topics related to vaccine safety before they became popular on social media
When I ask data/statistics experts such as Joel Smalley and Professor Norman Fenton whether they’ve seen any credible data proving the vaccines are safe and effective, they are unable to cite a single reference.
A local news station (WXYZ-TV) asked people to report on unvaxxed loved ones that became sick and died and instead they got hammered with hundreds of thousands of people saying they lost loved ones to the jab. See my video on the WXYZ-TV story and also this video.
Woman collapses and dies 7 minutes after Booster shot… The stunning thing is the Twitter video documents that the pharmacy workers have been instructed to not bring it up when briefing patients and, if asked, not to comment on the death. Do you think they are looking out for your best interest by withholding adverse events like death 7 minutes after the shot from the public? That should never happen. Have you ever seen a video like this before the COVID vaccines rolled out? The death was ruled as “natural causes” which means it was from internal organ failure as opposed to being hit by a truck. However, the internal organ failure was due to an external event (vaccinated).
A reader wrote: I work in the financial services industry in Toronto. A co-worker of mine was recently diagnosed with cancer. He has been getting treated at Sunnybrook hospital for it. The doctors there told him they’ve seen a significant spike in cancer cases well above what could be explained by people missing getting screened due to the pandemic. What’s more though is that they catalogue the vaccine status of every cancer diagnosis and the spike in the number of cases is only occurring in those who are vaccinated– apparently they are researching it to try and find out why the vaxed have seen a spike in cancers vs the unvaxed who haven’t- obviously they are not ready to go public with this but they know about it and are researching it fwiw
Books
Turtles all the way down: Vaccine science and myth shows the vaccines are not nearly as safe as people think. This is the most damaging book ever written showing the safety of the vaccines is highly questionable. There isn’t a single risk-benefit trial on all cause mortality and morbidity vs. placebo for any of the 70 approved vaccines even though they’ve had 60 years to do this. If the vaccines are truly beneficial, why do you think it’s never been done for any vaccine? A team of Israeli scientists wrote this book over 5 years. It was recently translated into English and is available through purchase on Amazon.
Dissolving Illusions: the history of vaccines shows they did a lot less than people think; probably next to nothing.
The Real Anthony Fauci: illustrates the corruption in the medical community today. For example, they created a more accurate adverse event reporting system (ESP:VAERS) system and then scrapped it after it showed all the vaccines were unsafe.
Once I established a policy of always recording calls with “fact checkers,” I’ve not had a single call from them trying to refute anything I’ve written.
None of the drug companies that make these products will refute anything I’ve written or supply a representative to debate me or any of my colleagues in a live debate. They have immunity from liability and they are not willing to be held accountable in the court of public opinion either.
This was a very well done study, but it is of course attacked by the pro narrative people. We’d love to have an open debate about this study, but the other side doesn’t want to talk about it in a neutral forum.
There is no study at all on the 6 foot distance rule. They just made that one up.
Origin of the virus investigation
Professor Jeffrey Sachs was tasked by The Lancet to lead an independent investigation into the source of the SARS-CoV-2 virus. After he determined it came from US biotechnology, all of a sudden nobody wanted to pursue the investigation any further.
Conflicts of interest
Tony Fauci gets paid every time you get a Moderna shot. He won’t disclose how much he makes and you can’t get via FOIA (it’s blacked out). If the Republicans get control of the Senate, that will change. Watch this video from Sept 20, 2022 of Rand Paul commenting on this as well as the well founded accusation that Fauci created the virus in the first place and then desperately tried to make it look like it came from nature after top scientists said it was a lab leak (watch the video at 2:00 onwards). Rand Paul called it, quite rightly, “the biggest cover-up in the history of science.”
The question you have to ask yourself is why is Fauci keeping his funding of the gain of function research and also his compensation for each vaccine dose a secret?
Tony Fauci was the primary reason that all early treatments were ignored by the government. It appears he did that because it would cut into his revenue stream.
Early treatment options
Early in the pandemic, two physicians, George Fareed and Brian Tyson, developed a treatment protocol using a variety of safe, low cost drugs and supplements with little to no side effects that had a near 100% success track record in preventing hospitalization, death, and long haul COVID if the patient started treatment shortly after realizing they were infected. They’ve treated over 10,000 patients. They wrote a best-selling book about it.
Today, more than two years later, the FDA and the CDC have not returned their calls.
Questions for lawmakers
Why can’t we have open forums where our public health officials can be challenged by experts who disagree? Is there proof that having open debate results in worse outcomes?
Why doesn’t anyone want to see the Israeli safety data?
Why isn’t anyone asking for Fauci’s unredacted emails?
Is there a scientific reason that the CDC is ignoring me and all the experts I work with?
Why hasn’t anyone calculated the minimum VAERS under-reporting factor (URF)?
Did the propensity to report change in 2021 vs. previous years. What is the new number in 2021 and 2022 compared to previous years? How did you calculate it?
Why do John Su and Tom Shimabukuro never talk about the URF in the ACIP meetings?
There were over 14,000 excess deaths reported in VAERS. That’s before the URF is applied. If these weren’t caused by the vaccine, what caused them?
If these vaccines are so safe, why are there more adverse events reported for these vaccines than for all other vaccines in history combined?
I found thousands of adverse events that are elevated by these vaccines compared to all other vaccines combined in previous years. How many adverse events did the CDC find?
There was a dramatic rise in adverse events reported in the VAERS system for the COVID vaccines. How could this not be a serious safety concern? The propensity to report did not increase. If you believe the propensity to report did increase, what data do you have to support that?
My neurologist has been in practice for 11 years. She has 20,000 patients in her multi-physician practice. In that time, she’s never had to report a single event to VAERS. With the COVID vaccines, she now needs to make 1,000 reports. If the vaccines are safe and effective and most all the symptoms are mild and short term, how do you explain this? Her event rate similar to the 4.5% injury rate that the Israeli MoH found. So her reporting rate is more than 10,000 times higher than for any other vaccine. Couldn’t that be the explanation for the higher rate of VAERS reports? Doesn’t this suggest that the propensity to report is much lower this year because there are so many more events and doctors simply don’t have the time to report them all?
The NEJM pregnancy paper by Tom Shimabukuro noted that the results on safety for pregnant women was preliminary since many of the women were still pregnant. What was the final result and why wasn’t it published?
There was an analysis of the VAERS data by Hannah Rosenblum published in the Lancet. It never goes into explaining why there were elevated reporting rates and also the nature of the reported events are not normal background events. Couldn’t the elevated reporting rates be caused by a dangerous vaccine? Does she want to look at the Israeli safety data? If not, why not? The Israeli data directly contradicts the conclusion of the paper. Shouldn’t we figure out which conclusion is correct?
Why does Carol Crawford not answer my questions about an open discussion with the top vaccine misinformation spreaders to resolve our differences and reduce vaccine hesitancy?
Why does Martha Sharan ignore my emails and phone messages when I attempted to ask for permission to talk to the authors of the Rosenblum paper? Can’t she reply with the reason questions are not allowed?
The unanswered questions
Questions I’d love to get the answer to. These were asked, but never answered.
The CEO of Moderna was asked how the 19 nucleotide sequence from a Moderna patent got into the SARS-CoV-2 genome. That sequence is never found in a virus. How did it get in this one? The CEO said he’d look into it, but never reported the explanation. I’d love to know what it was.
Why hasn’t any Democratic committee chairman asked the NIH for Tony Fauci’s unredacted emails? Don’t we want to know the truth about whether there was a deliberate cover-up? If there was, shouldn’t Fauci be fired?
Fauci wasn’t supposed to be funding gain of function research but he was. How is he being held accountable?
How much is Fauci making every time someone gets a Moderna shot? He’s a public official… Why is this a secret?
Debates
People who disagree with the mainstream narrative are rewarded with censorship, permanent bans on posting on social media, demonetization of your YouTube account, revocation of your medical license, revocation of your medical certifications, loss of hospital privileges, loss of job, loss of funding, loss of friends, and a Wikipedia entry labeling you a “misinformation spreader” and/or “conspiracy theorist.”
This is a problem. I am not aware of any paper published in the medical literature that shows that such tactics result in better health decisions.
Should we use the same rules at the UN when nations disagree? Do you think that will result in better outcomes?
The way people resolve differences is by confronting the issues and talking through them. But we are not doing this:
This is objective proof of a broken system. It is indefensible. Caught on video camera. There is no reason that anyone in a position of authority on the COVID vaccines would refuse an opportunity to see the most thorough post-vaccine safety study ever done: one that shows causality of serious adverse events.
Rechallenge changes a causal link “from possible to definitive,” Dr. Mati Berkovitch, head of the research team and a pediatric specialist, said at the meeting.
and
Many of the reported adverse events were found to be long-lasting, which researchers said in the meeting was surprising since the brochure handed to vaccine recipients says otherwise. They also said Pfizer officials told them that Pfizer did not know of any long-lasting symptoms.
and
In the official report later issued to the public, the MoH did not detail how researchers were caught off guard by the duration of the events and side effects. The health agency also stated that there were no new events identified.
It concludes:
The choice to omit some of the crucial findings discussed in the meeting from the public report is “a recipe to destroy” the entire vaccine program, according to Levi, an Israeli native and an expert in risk management.
“The more pro-vaccine, the more disturbed you need to be from something like this,” Levi told The Epoch Times. “And the reason is that the two most important enablers for vaccine programs … to be successful is trust and transparency, that you actually communicate to people the real risk-benefits and allow them to make choices about what they want to do. The second thing is that you take care of the people that were harmed by the vaccine because no vaccine has 100 percent safety.”
“I think we have in this example … where we violate these two very important principles,” he added. “This is a recipe to basically destroy all vaccine programs, so the more pro-vaccine you are, you should be more disturbed by this.”
How can you have the chair of a safety committee not interested in seeing important safety data? Professor Grace Lee should be removed from her position by the CDC. Why isn’t she? Does anyone care?
Why does Dr. Paul Offit ignore requests to see the same data?
According to the Epoch Times article, everyone declined to comment on the story: the scientists, the MOH officials, and the CDC’s Immunization Safety Office declined to comment on the Israeli findings.
Meta-collections
If the above isn’t enough, there are hundreds more “hard to explain” data points.
There is an excellent article written in August 2020 by Norman Doidge entitled “Medicine’s Fundamentalists” which talks about the “all-available-evidence approach.” It should be read by every doctor in America. This is how medical science should work.
The precautionary principle of medicine
The precautionary principle medicine seems to have been thrown under the bus during the pandemic. It says in the face of uncertainty, one should take reasonable measures to avoid threats that are serious and plausible.
For example, the Pfizer clinical trial showed the vaccine saved only one COVID death per 22,000 injected. That means we might only save around 10,000 lives if we inject 200M Americans. So if VAERS, which is at least 41 times under reported, is showing over 12,000 deaths associated with the vaccine, any reasonable person should say that killing more than 41 people to save 1 life is nonsensical… shouldn’t we put a PAUSE on this intervention until we resolve the uncertainty?
In the current system, questioning the CDC or other authorities results in serious retribution as mentioned earlier.
Is that really the right way to handle scientific dissent?
Summary
Are the vaccines “safe and effective” as claimed?
To answer this, science requires that we look at all the available data and see whether the data is more consistent with the hypothesis of “safe and effective” or “not safe and effective.”
All the data that I and my colleagues have seen end up being placed in the “not” bucket.
We are open to being shown we got it wrong on the hundreds of pieces of evidence we have examined, but nobody is willing to discuss the data with us to resolve the issue, not even for $1M dollars.
Twenty years ago, the “Cheney-Bush junta” — as Gore Vidal called it — launched its propaganda campaign to invade Iraq, effectively casting the dye for much of the historic period since.
The same day, then Vice President Dick Cheney appeared on Meet the Press with Tim Russert, hyping the New York Times story as evidence that Hussein was attempting to acquire “the kinds of tubes that are necessary to build a centrifuge and the centrifuge is required to take low-grade uranium and enhance it into highly-enriched uranium which is what you have to have in order to build a bomb.” Colin Powell and Condoleezza Rice followed Cheney’s lead on other shows.
In 2005, I confronted Miller about her reporting, asking her at if she would name the anonymous lying source who she allegedly relied on to falsely report “the best technical experts and nuclear scientists at laboratories like Oak Ridge supported” the CIA claim that the tubes were for a nuclear weapons program. In fact, it would later be established, the nuclear scientists did not support such an assessment and were effectively muzzled. When I questioned her, Miller refused to name the source that fed her this false information and Marvin Kalb, the moderator of the event, see video, ran interference, stopping further follow-ups. (See my piece “Should Media Expose Sources Who Lied to Them?”)
Many serious analysts early on deduced that the source was Cheney himself, likely through his chief of staff, Scooter Libby.
Even the mainstream Bob Simon of CBS would later remark to Bill Moyers about Cheney: “You leak a story, and then you quote the story. I mean, that’s a remarkable thing to do.”
Remarkable is actually an understatement. It’s engaging in a de facto conspiracy to deceive the U.S. public into war.
In April of 2020, a journalist asked at the daily White House press briefing: “Mr. President, I wanted to ask Dr. Fauci: Could you address these suggestions or concerns that this virus was somehow manmade, possibly came out of a laboratory in China?”
Anthony Fauci replied: “There was a study recently that we can make available to you, where a group of highly qualified evolutionary virologists looked at the sequences there and the sequences in bats as they evolve. And the mutations that it took to get to the point where it is now is totally consistent with a jump of a species from an animal to a human.”
That article was widely accepted by the major media as eviscerating the possibility of lab origin of Covid, shutting down debate at that critical time and continuing to hinder it to this day.
The thing is, Fauci seems to have had a serious role in that article’s appearing.
In 2021, limited Freedom of Information Act findings showed that Fauci had at minimum effectively coordinated with the named authors of the Nature Medicine article. See Nass’ write-up and subsequent reporting by some mainstream outlets such as USA Today.
Thus, this insidious tactic of helping to plant a story pushing the line you want in a media outlet and then citing it as evidence for your case was employed by both longtime creatures of Washington at historic junctures.
There are other notable parallels. Both Fauci and Cheney have also both been leading beneficiaries of Trumpwashing.
Ashley Rindsberg makes some serious arguments in his piece, “How Dick Cheney created Anthony Fauci,” including about the buildup of US bio“defense” after 9/11 (actually the anthrax attacks) — a trend several observers have noted. Alexis Baden-Mayer traces such arguments back to 1976, when Cheney and Donald Rumsfeld apparently pressured President Ford to order massive inoculations in the Swine Flu scare, which he would be widely mocked for.
While the antiwar forces and “left” criticism of the Iraq WMD propaganda were wholly inadequate, they at least manifested themselves on the national stage to some extent. Covid origins has hardly been recognized as an antiwar issue by most and the “left” at times has actually played a detrimental role, explicitly doing the establishment’s bidding in irrationally denying or minimizing the possibility of lab origin of the pandemic.
One thing that should be kept in mind as one parses through the claims and “exposés” is that some are de facto cover stories.
The Bush administration ramped up their propaganda campaign for the Iraq invasion, as noted at the beginning of this article, in September of 2002.
Why then? Sophisticates at the time would quote Andrew Card: “From a marketing point of view, you don’t introduce new products in August” said Bush’s chief of staff.
With the Bush administration cynically using the one year anniversary of 9/11 as a backdrop to launch their push for invading Iraq, the rationale articulated by Card was actually a remarkably benign motivation, a likely cover, in comparison to the war makers actual thinking.
In the face of incessant media badgering to rush out and take the latest version of experimental coronavirus “vaccine” shot — the “bivalent” booster, the vast majority of Americans are saying “nope” and continuing on with their lives. Three weeks into the all-out push to have every American over 12 years old take the new shot (giving these new booster shots to younger children is up next), it appears that less than two percent of eligible Americans have done so.
The growing resistance to the coronavirus shots pushers’ propaganda gives one hope for America. With each new experimental coronavirus shot Americans are being urged to take, the percentage who acquiesce declines. The line that the shots are needed, safe, and effective has proven a farce on all counts. And the latest shot rushed into distribution has taken the previous shots’ mockery of the process for ensuring safety and efficacy to the next level. The truth is out there; increasingly Americans are seeing past the media hype and finding it.
Yet, despite their great power over what people can say, fact checkers are also increasingly frustrated at calls for more transparency about the way they operate and say they are being bombarded with freedom of information act (FOIA) requests and lawsuits.
The fact checkers say these requests and lawsuits are meant to drain the resources of climate change researchers and to discourage them from doing their work which is, in turn, an attempt to shut down their own speech.
“They make a point of going after the fact-checkers because, in addition to stopping regulation, they also want to prevent or discourage climate scientists from doing things that might educate the public,” said Lauren Kurtz, Climate Science Legal Defense Fund’s executive director to Bloomberg.
Kurtz’s organization provides climate researchers with legal assistance. They assist about 40 researchers annually. But this year has been busier, as they have already assisted 35 people.
One of the beneficiaries of the fund is Doug MacMartin, who was sued by Dane Wigington after he fact-checked his documentary “The Dimming,” which, according to MacMartin, is filled with conspiracy theories.
On the science fact-checking website Climate Feedback, used by social media companies to flag what it sees as science misinformation, MacMartin described Wigington’s documentary as “pure fantasy.” The plaintiff sought $75,000 in damages from MacMartin, arguing that the fact-check reduced the visibility of his documentary on Facebook, hurting its revenue.
“I mostly felt disbelief,” MacMartin recalled to Bloomberg. “A bit of shock combined with, ‘I just don’t have time for this.’”
Earlier this month, a federal court dismissed Wigngton’s lawsuit, but he plans to appeal.
Daniel Swain, a climate researcher at University of California, Los Angeles, had to deal with a FOIA request filed by a group called Energy Policy Advocates. Swain is vocal about droughts and fires in Western US. The requests sought text messages, encrypted messages, and emails related to a fact-check written by Swain and others about the book “Unsettled: What Climate Science Tells Us, What It Doesn’t, and Why It Matters,” by Steven Koonin, who worked in the Department of Energy during Obama’s era.
Swain challenged the requests using a university lawyer, arguing that it had the “presumptive intent of disrupting primary research and outreach activities by inundating climate scientists.” The records department said that the motivations of the requester were irrelevant, but was bound by law to provide the information requested.
“I spend nights and weekends compiling and going through thousands and thousands of emails because these requests are extremely broad,” he said. “In some cases they’re essentially open ended: they’re asking about multiple years, multiple keywords and multiple platforms.”
The group filing most of the requests are Government Accountability and Oversight, and Energy Policy Advocates. The two groups go by the acronyms GAO and EPA, the same acronyms used by federal agencies Government Accountability Office and the Environmental Protection Agency.
Climate Feedback and Meta are facing a $2 million lawsuit filed by Libertarian commentator John Stossel who was censored on Facebook as a direct result of a post by the fact-checker.
Climate Feedback flagged Stossel’s video “Government Fueled Fires” about the wildfires in California in 2020. The fact-check resulted in Facebook limiting the visibility of the video and we have more information on that case here.
World-renowned Critical Care Specialist, Dr. Paul Marik, joins Del to talk about the harrowing fight to keep his medical license, after treating critically-ill Covid-19 patients with lifesaving early treatments that were against hospital policy. Fellow FLCCC co-founder, Dr. Pierre Kory, joins the conversation to reflect on their first battle against Academia; the shocking struggle with a corrupt medical system to utilize a life-saving, cheap, and safe protocol for sepsis, the leading cause of death in the world.
“I have tested positive for COVID. I’m feeling well & symptom free. I’ve not had the new bivalent booster yet, as I was following CDC guidelines to wait 3 months since my previous COVID case which was back in mid-August. While we’ve made great progress, the virus is still with us.”
Mr. Bourla had his previous Covid infection in mid-August. Now he tested positive for Covid again, only a month after his previous illness. Albert is very lucky to be protected by his vaccine and previous booster doses!
Pfizer’s CEO says that he did not yet get the bivalent booster, because he wanted to wait 3 months after his most recent infection.
So, the CDC said that Bourla had a “low risk of reinfection” for three months after his last Covid — but Bourla got Covid a mere month after his previous infection.
Albert is not alone. Here’s a Redditor who is having his or her FIFTH Covid in 1.5 years:
Covid is not going anywhere.
Apparently, it is again rising strongly in the UK. The United States is usually about a month behind the UK. So, for now, the US is in the “Covid is over” phase.
A judge this month is hearing evidence in a lawsuit filed in 2011 by a group of individuals who developed cancer, allegedly as a result of radiation from their cellphones. Depending on how the judge rules, the lawsuit could finally head to a jury trial.
Evidentiary hearings in Murray v. Motorola began Sept. 12 in the Superior Court of the District of Columbia, and are scheduled to continue until Sept. 30. Expert testimony will be presented during the hearings before the case goes before a jury.
In a parallel case that may have repercussions for the D.C. case, a similar lawsuit before a federal court in Louisiana — filed by the widow of a man who died of an aggressive form of brain cancer allegedly caused by cellphone radiation — also is headed to trial.
The D.C. case is proceeding without the plaintiffs being able to present a significant category of evidence pertaining to the defendants’ liability. However, that evidence will be heard in the Louisiana case.
In an exclusive interview with The Defender, Hunter Lundy, a lawyer representing plaintiffs in both cases, discussed the evidence and expert testimony and the potential significance rulings in this case could have.
D.C. case: lawsuit filed in 2001 finally headed to a jury
The six plaintiffs had developed brain tumors beneath where they held their cellphones. Additional plaintiffs joined the case in 2010, 2011 and thereafter — with the number of plaintiffs now exceeding 80, according to Lundy.
The defendants are a who’s who of major telecommunications companies, including AT&T, Bell Atlantic, Bell South, Motorola, Nokia, Qualcomm, Samsung, Sanyo, Sony, Sprint, T-Mobile, Verizon and many other companies.
The lawsuit also names the Federal Communications Commission and the Cellular Telecommunications Industry Association (CITA), an industry lobbying group.
After 21 years and multiple delays, many of the plaintiffs have since died.
Despite efforts on the part of the defendants to get the lawsuit dismissed or relocated to federal court in Maryland, the case was initially remanded from the D.C. District Court to the D.C. Superior Court — where the complaints were dismissed in 2007, before being partially reinstated in 2009, by the District of Columbia Circuit Court of Appeals.
The case continued to wind through the courts, with evidentiary hearings finally beginning this year.
Lundy discussed key details about the lawsuit, stating that the plaintiffs alleged: “the radiation frequency … the microwave radiation coming out of cellphones increased the risk of individuals getting brain tumors.”
The plaintiffs further alleged that “the cell phone industry, the manufacturers and the carriers knew when these [cellphones] were put out on the market that they had dangers that they didn’t warn people about,” said Lundy.
However, Lundy said that the main thrust of the case concerns gliomas — tumors that impact the brain and spinal cord.
According to Lundy, “There are several kinds of gliomas … the most prevalent one is the glioblastoma,” a type of malignant glioma.
Other gliomas, such as acoustic neuroma, are benign, Lundy told The Defender, but form on the cerebral nerve inside the brain, growing without their victims being aware of them. Eventually, their growth leads to hearing loss and their removal results in residual brain damage.
Ultimately, most such cases result in death, said Lundy. With glioblastoma, for instance, diagnoses range from having three to four months — to five years at most — to live.
“There’s not a lot of optimism when you get a glioblastoma,” said Lundy. “And so, whether it’s directly or indirectly, [the gliomas] have a genotoxic effect which will end up having a mutagenic effect and then a tumor coming out of it.”
Referring to the plaintiffs in the D.C. case, Lundy said, “Many of them have died, and many of the cases are just death cases right up front, or the widows or family members brought the suits.”
“This is what the battle is [about] … that’s our case in a nutshell,” explained Lundy.
The victims were impacted by first-, second- and third-generation analog cellphones produced in the 1980s and 1990s. “The antennas were up at the top of the phone and some of them were operated on three watt and greater power,” Lundy said, whereas “Today you’ve got smartphones operating on a quarter watt.”
Lundy told The Defender :
“There was a long period of years in which people were getting high exposure from cellphone radiation because they were using them so much … and there wasn’t sufficient information, instruction or warning by the industry to the user of the dangers involved. That’s the thrust of the case.”
“Our argument is that if you continue to use the analogue [phones] and you use the second- or some of the third-generation [devices], you’ll see a linear effect” regarding radiation exposure and latency, Lundy added, where the effects of such radiation become apparent over time.
As an example, Lundy referred to the bombings of Hiroshima and Nagasaki during World War II, where “it was still 40 years before … you saw tremendous numbers of cancers developing.”
Although the plaintiffs were from different parts of the U.S., the initial lawsuits — later combined into the current case — were filed in the District of Columbia “because [of] the idea that the lobbying institutions of the wireless industry [are] located in D.C.,” said Lundy.
However, these lobbying groups — and the rest of the defendants — “don’t want us to have a trial in front of a jury,” said Lundy, which resulted in the defendants using a variety of delay tactics.
In 2013, a Frye hearing was held, during which, according to Lundy, the plaintiffs’ expert witnesses “had to pass a standard before they could testify in front of a jury.”
“The Frye standard had to be met where you proved that the methodology used by the expert … was generally accepted in the scientific community,” Lundy said.
In the period between 2013 and 2015, the five experts put forth by the plaintiffs were approved according to the Frye standard and a trial was held, Lundy said. However, the defendants, on appeal, were able to get the case reversed and to get the standard by which the plaintiffs’ experts were evaluated changed, to the Daubert standard.
According to Lundy, in this second standard, “you had to prove that not only was the science [accepted], you had to prove that it was reliable and that it was readily available.”
“In the interim,” according to Lundy, “we have been through several judges.”
Ultimately, the plaintiffs were not allowed to supplement the opinions of the initial experts with new witnesses and new science, unless it “somehow [was] related to the old opinion,” Lundy said. This hamstrung the plaintiffs and subsequent judges hearing the case, he added.
But “We’re going forward with other witnesses … and then the case will be submitted to the court again and there will probably be post-hearing briefs,” Lundy said. “At some point, the court will make a ruling and then both parties will have a right to appeal … and so, the process goes on.”
Louisiana case an opportunity for more expert testimony to be presented
The related case, Walker v. Motorola et al., filed in the U.S. District Court for the Western District of Louisiana, may present an opportunity for plaintiffs to present expert testimony that was shut out of the D.C. case.
According to Lundy, this lawsuit has the potential to quickly go to trial.
“Ahead of what’s going on in D.C., we just want a case to go to trial somewhere … we need a ruling before people go forward,” Lundy told The Defender.
Referring to the D.C. case, Lundy said:
“We haven’t been able to get … liability document production, discussing the development of the products, the interaction between risk management and others.
“So I think in Louisiana, if we prevail, we will get the discovery [of such evidence]. It’s a different ballgame.”
In the Louisiana case, the family of Frank Aaron Walker sued the telecommunications industry, alleging the pastor’s death from an aggressive brain cancer was brought on by cellphone radiation, the health risks of which the industry has known for decades.
According to the suit, the telecommunications industry “suppressed credible cell phone safety concerns and has conspired to conceal or alter results of safety studies to make them more ‘market-friendly.’”
Walker was “a 25-year user of cell phone products,” the suit claims, before dying on Dec. 31, 2020, age 49, following “a two-year battle with glioblastoma that included extensive radiation, chemotherapy and surgery.”
During this two-year period, Walker experienced severe symptoms including “seizures, visual auras, excessive fatigue, migraines, light sensitivity, memory problems, psychological and emotional stress, anxiety, and depression,” the lawsuit alleges.
Similar to the D.C. case, the defendants in the Louisiana lawsuit include several major telecommunications industry players, such as AT&T, Cricket Communications, CITA, Motorola, the Telecommunications Industry Association and ZTE.
In a 2021 press release issued after the lawsuit was filed, Lundy stated:
“For generations, the telecom industry has fought the release of scientific studies and information regarding ties between mobile phone use and brain tumors. The industry manipulated the science to the detriment of consumers.
“With this lawsuit, Mr. Walker’s family hopes to help reveal the telecom industry’s secrets and hold them accountable for harm done to consumers.”
In the same release, Lundy alleged the telecommunications industry “downplayed, understated, and/or did not state the health hazards and risks associated with cell phones.”
The press release also quoted Walker’s widow, April Marie Walker:
“Throughout his battle with cancer, Frank never lost his faith or his sense of humor, but he suffered terribly.
“Our family’s hope now is that we can force the telecom industry to let consumers make informed choices about the products we buy.
“If the telecom industry knew holding a cell phone next to one’s head is dangerous, then the public should have known this information.”
In remarking on the broader significance of this case, Lundy said:
“There needs to be an exposure of truth. I just believe everybody should be accountable.
“We have not been allowed to do liability discovery. We have done scientific discovery and evidence about science. But we do not yet have the industry’s documents.
“I think we’ll be able … to do liability discovery here in federal court in Louisiana when we go forward.”
Industry concealed studies linking cellphone use to brain and DNA damage, plaintiffs allege
The Louisiana lawsuit also cites a significant number of scientific studies and industry actions taken since the 1980s, “including the firing, defunding or denigration of researchers who discovered adverse effects associated with cell phone use.”
“At all times herein mentioned, Defendants were aware of numerous studies and experiments that demonstrated the health hazards of RF radiation dating back to the late 1940s and continuing to this day, yet Defendants have consistently maintained to the public at large that cell phones are absolutely safe.”
The lawsuit alleges “scientific and medical research, published in peer-reviewed literature, has demonstrated a correlation between biological effects and the exposure to RF radiation within the radio frequency band of 300 megahertz to 2.4 gigahertz,” noting, however, that such peer-reviewed journals are not typically read by the general public.
Radiation exposure standards adopted by the American National Standards Institute (ANSI), initially in the 1960s, and subsequently modified in the 1980s and 1990s, “excluded cell phones,” states the lawsuit, as “the cell phone industry manipulated the research and pressured members of the ANSI Safety Committee to exempt cell phones from regulation and compliance.”
However, as scientific and public concern over radiation produced by cellular phones increased in the 1990s, “defendants, individually and through their trade associations … undertook with public fanfare to fund scientific studies to prove the safety of cell phones,” resulting in the formation of the Scientific Advisory Group in 1993.
Subsequently, industry associations CTIA and Telecommunications Industry Association hired an expert, Dr. George Carlo, to direct the Scientific Advisory Group and conduct research into cellular phone radiation. However, as the lawsuit states:
“When this industry-funded research failed to corroborate the industry’s claims of safety and, in fact, presented new evidence supporting health concerns, the industry responded by terminating the research funding and publicly disparaging Dr. Carlo as well as suppressing and minimizing the results of his studies.”
Nevertheless, numerous other scientific studies followed, calling into question the industry’s claims regarding the safety of their mobile devices. These studies are cited in the lawsuit and include:
A 1995 University of Washington study conducted on rats exposed to “radiation similar to the type of radiation emitted from the antenna of a cell phone,” found the radiation caused damage to DNA. The industry funded research that aimed to disprove these fundings, but which ultimately confirmed them, leading the industry to refuse to publish the results.
Another scientist who subsequently replicated the DNA damage found by the University of Washington research had his findings “suppressed” by the industry, pressuring him and threatening to withdraw funding.
A 1996 study of Air Force personnel found those exposed to RF radiation had a “risk of brain tumors 1.39 times higher … versus those not exposed.”
A 2000 study by Sweden’s Orebro Medical Center “found the risk of tumors developing on the same side of the head cell phone users hold their cell phones is significantly higher than it is for the other side.”
In 2000, the World Health Organization (WHO) launched a decade-long multinational research study, the “Interphone Study,” ultimately finding that “the use of cell phones for a period of 10 years or more can increase the risk of glioblastomas by 40% in adults” and that “tumors are most likely to occur on the side of the head most used for calling.”
A 2002 Swedish study found “the risk of developing brain tumors from first-generation cell phones … was as much as 80% greater than those who did not use cell phones.”
Another Swedish study, in 2003, published in Environmental Health Perspectives, a journal of the National Institute of Environmental Health Sciences, which in turn operates under the aegis of the U.S. Department of Health and Human Services, “found electromagnetic fields (EMFs) emitted by certain cell phones damaged neurons in the brains of rats.”
A four-year study performed by Reflex, with funding from the European Union, in 2004 found that “radio waves from cell phones damage DNA and other cells in the body and that the damage extended to the next generation of cells.”
The lawsuit adds, “mutated cells are considered a possible cause of cancer,” and that the radiation levels tested in the study were within the range used by most cellphones at that time. The study ultimately “advised people to use landlines, rather than cell phones, whenever possible.”
A 2005 study “reported using a cell phone in rural areas might lead to the development of brain tumors.” As cellphone towers are more sparsely placed in rural locations, cellular devices tend to use higher wattage in order to achieve reception of a mobile signal.
A 2009 meta-analysis of 465 scholarly studies involving the relationship between cellphone radiation and cancer, published in the Journal of Clinical Oncology, “demonstrated a significant positive association between cell phone use and cancer” and “established the association increased with long-term cell phone use.”
A hearing held by the U.S. Senate Committee on Appropriations and the Subcommittee on Labor, Health and Human Services, and Education and Related Agencies in 2009 featured testimony from an investigator involved in the Interphone Study that was also published in the American Journal of Epidemiology.
According to the expert, there was “an elevated risk of salivary gland tumors was seen among people who used cell phones for more than 10 years, especially when the phone was usually held on the same side of the head where the tumor was found, and when use was relatively heavy.”
In 2011, the WHO’s International Agency for Research on Cancer (IARC) “declared the RF radiation emitted from cell phones to be ‘possibly carcinogenic to humans.’”
Also according to the lawsuit, in the period since the IARC’s 2011 declaration, “more than 1,000 additional scientific studies have been published in peer-reviewed literature further supporting the causal link between cell phone radiation, brain tumors and health effects.”
The lawsuit states that “several experts have analyzed this new information and concluded cell phone radiation should be classified as a ‘probable human carcinogen.’”
Some of these subsequent studies include:
A 2015 study out of Jacobs University in Germany, finding (and replicating the results of a 2010 German study) that “weak cell phone signals can promote the growth of tumors in mice,” at “radiation levels that do not cause heating and are well below current safety standards.”
A 2016 study by the U.S. National Toxicology Program, finding that “male rats exposed to cell phone radiation developed higher rates of cancer” and also “caused DNA breaks in the male rats’ brains.”
Remarking on these studies and on the type of testing performed by the telecommunications industry with regard to radiation produced by cellular phones, Lundy told The Defender :
“We know that, for instance, the cellphone industry, the cellphones are supposed to pass a standard called SAR — Specific Absorption Rate. They did these [tests] on mannequins.
“There’s nothing wrong with the standard. But the way they test it to comply with the standard was wrong. And they used 6’2” male mannequins to determine whether or not these phones were passing SAR, and that’s so unrealistic.
“And they’ve got instructions telling people, don’t hold [mobile devices] firm against you, hold it 5/8 of an inch away from your head. Well, nobody knows that they weren’t doing that in their mannequin testing.”
However, according to Lundy and to the lawsuit, the telecommunications industry tacitly began to address these concerns beginning in the late 1990s and early 2000s.
Lundy told The Defender that “the fact that they, in the late 1990s and early 2000s, as they started making patent applications to change the design of their phones, started to move the antennas because they had a problem,” is indicative of this shift, adding:
“And we know enough to know that the London [insurance] market quit writing coverage for the wireless industry in the early 2000s, so they know something and are seeing something that we haven’t seen.”
The Louisiana lawsuit cites 13 examples of the telecommunication industry’s moves to quietly reduce RF exposure from mobile devices, dating back as early as 1991.
Lundy noted that, in the D.C. case, expert witnesses from Europe, including epidemiologists and cell biologists from countries such as Austria, Greece and Slovakia, were initially the most willing to come forward with testimony, adding, however, that “American scientists are now on board.”
Lundy: ‘The truth is going to come out’
Lundy said he’s frustrated with the legal proceedings’ slow pace:
“It’s just disappointing that the scales of justice turn so slowly. And you know, sometimes that’s the case. There’s no justice.
“But the truth is going to come out. It’s coming out now. I mean, sometimes [it] doesn’t always come out in the timing that we want it to come out, but it will come out.”
Lundy cited the long history of lawsuits involving the tobacco industry as an example of this, saying:
“The cigarette industry never lost a case for 30 or so years. But when [tobacco industry whistleblower] Dr. Jeffrey Wigand disclosed the fact that they were manipulating nicotine to addict 13-year-olds, I mean, the whole climate shifted.”
According to Lundy, truthful information regarding children’s health, in relation to the use of cellular phones, is of particular importance:
Lundy told The Defender :
“There’s other countries … that have barred the use of cellphones for kids that aren’t 16 years of age yet … we know that the skull is not fully developed until they’re 25. So we’re talking about children having radiation going into their brain very young.
“So it’s about information. It’s about warning. It’s about telling people the truth. It’s not about money over that.”
Overall, for Lundy, the broader significance of the D.C. and Louisiana cases and their outcome concerns “educating people.”
He said:
“The significance is going to educate the world. It’s going to educate people that at these radiation frequencies from these devices … they increase the risk.
“We just want to be informed. How can we be a free nation and exercise our freedom when we’re not told the truth? And I’m not trying to be political, but that’s just a fact. We’ve got a world of misinformation and it’s motivated by greed.”
Michael Nevradakis, Ph.D., is an independent journalist and researcher based in Athens, Greece.
This claim originated from the World Weather Attribution group, who regularly publish such claims every time there is some bad weather. They base their conclusions on computer models, not on real world data. If they had looked at the actual data, they might have come to different conclusions.
According to the Pakistan Meteorological Department, most of the excess rain in August arrived on 18th/19th and 25th/26th. In fact 41 per cent of the month’s rainfall fell on these four days:
The cause of this heavy rain was two tropical storms, which had crossed from the Bay of Bengal – BOB 06 and BOB 07. (In the Indian Ocean they are categorised as a ‘depression’ and ‘deep depression’. in Atlantic storm terminology, these would be called a tropical depression and a tropical storm respectively).
Both storms followed identical routes west from Bengal, tracking over Rajasthan before hitting the province of Sindh, the region worst affected by flooding:
Unusually, these storms did not dissipate after landfall in Bengal so wreaked havoc for days afterwards. Pakistan, needless to say, is not immune to tropical cyclones. But for two storms to hit in the space of a week, at the same location, and during the wettest month of the year is an extremely rare combination of meteorological events.
Pakistan was already experiencing a wetter than normal monsoon, courtesy of La Nina, but those two storms pushed the rainfall into record territory, the wettest August since 1961.
There is no evidence that tropical cyclones are getting more frequent or intense in the Indian Ocean, so consequently there is also no evidence that last month’s rainfall had anything to do with climate change.
What is significant, though, is the chart of annual rainfall in Pakistan, published in the State of the Pakistan Climate 2021:
Annual rainfall was clearly much less during the 1960s and 70s, the direct result of global cooling at the time. Those years of drought were a disaster for Pakistan, and the country has welcomed the increase in rainfall since, just as they do across the border in India. The wetter, the better!
It is also significant that the seven-year moving average has barely changed since the 1980s, fluctuating up and down, but with no obvious long-term trend. If global warming was really bringing more extreme rainfall, we should expect to see evidence of this in the annual figures.
You will of course hear none of this from the BBC or the climate attribution industry, which was established to promote the climate change agenda, and which routinely publishes patently unsupportable claims.
Steve Koonin, President Obama’s climate scientist, puts it best: ‘Practitioners argue that event attribution studies are the best climate science can do in terms of connecting weather to changes in climate. But as a physical scientist, I’m appalled that such studies are given credence, much less media coverage. A hallmark of science is that conclusions get tested against observations. But that’s virtually impossible for weather attribution studies. It’s like a spiritual adviser who claims her influence helped you win the lottery – after you’ve already won it.’
Of course, like most of climate science, the climate attribution industry has little to do with science, and everything to do with money.
The Arctic ice scam
FOR years the ‘experts’ have been telling us that the Arctic would soon be ice-free in summer.
Al Gore notoriously warned us in 2009 that ‘there is a 75 per cent chance that the entire north polar ice cap, during the summer months, could be completely ice-free within five to seven years.’
He was, of course, just a politician. But a whole host of supposed Arctic scientists were all busy issuing similar warnings at the time. In 2007, for instance, Professor Wieslaw Maslowski told us that northern polar waters could be ice-free in summers within just five to six years. In December that year, Jay Zwally of Nasa agreed, giving the ice till 2012. A year later, in 2008, Professor David Barber went one step further, saying the ice would all be gone that very summer.
For sheer persistence in getting it wrong, however, the prize must go to Peter Wadhams, Professor and Head of the Polar Ocean Physics Group in the Department of Applied Mathematics and Theoretical Physics at the University of Cambridge:
• In 2012, he predicted that the Arctic would be ice-free by 2015/16.
• In 2014, he thought it might last till 2020.
• In 2016, he confidently predicted the Arctic would be ice-free that summer (though curiously he now defined ‘ice-free’ as less than 1 million square kilometers).
All these pronouncements were designed for political propaganda purposes, not for scientific reasons, and were widely propagated by the gullible media.
For instance in an article in the Independent in June 2016 (complete with photos of a cute polar bear on a melting piece of ice) Wadhams confidently asserted: ‘My prediction remains that the Arctic ice may well disappear, that is, have an area of less than one million square kilometres for September of this year. Even if the ice doesn’t completely disappear, it is very likely that this will be a record low year. I think there’s a reasonable chance it could get down to a million this year and if it doesn’t do it this year, it will do it next year.’
Unfortunately for Professor Wadhams, the sea ice has not been melting away as ordained. On the contrary, it has been remarkably resilient. Arctic sea ice has just reached its minimum extent this week, just as it always does in September, and the provisional data shows that there is still 4.7million sq km of the stuff.
As can be seen from the chart below, this year and last had the largest extents since 2013 and 2014, and there is considerably more ice around this year than in 2007 and 2008.
There was a climate shift in the Arctic in 2007, when warm Atlantic waters entered the Arctic basin and ocean currents pushed a lot of the thicker multi-year ice out through the Fram Strait, which lies between Greenland and Svalbard, into the open Atlantic Ocean, where unsurprisingly it melted. Since 2007, much of the ice has consequently been thinner, new ice, which naturally tends to melt in summer.
Climate scientists with an agenda to peddle jumped on the bandwagon and predicted that the ice would just carry on melting. However, they ignored the lesson of history. The Atlantic Ocean regularly goes through such cyclical events, with cold and warm phases lasting about 50 to 60 years. The cycle is called the Atlantic Multidecadal Oscillation, or AMO, and it is known to have been occurring for at least the last 1,000 years.
In the 1970s, climate scientists were extremely concerned about the increase in sea ice in the Arctic, which occurred during the cold phase of the AMO. The leading climatologist of his day, H H Lamb, wrote in 1982: ‘Agreatly increased flow of the cold East Greenland Current has in several years (especially 1968 and 1969, but also 1965, 1975 and 1979) brought more Arctic sea ice to the coasts of Iceland than for 50 years. In April-May 1968 and 1969, the island was half surrounded by ice, as had not occurred since 1888.’
Satellite monitoring of Arctic sea ice began in 1979, at the depth of the cold period. The climate mafia always use this period as the baseline, pretending it was the ‘norm’. That way they can attempt to fool the public that the warming in the Arctic and loss of ice since then is due to man-made global warming.
What is astonishing is that these buffoons are still in a job and living off the taxpayer. In any other field of science, to be so consistently wrong for so long would have quickly led to a well-earned oblivion.
By F. William Engdahl – New Eastern Outlook – 11.04.2022
Amid the ongoing global inflation crisis, NATO heads of state and mainstream media repeat a mantra that high energy prices are a direct result of Putin’s actions in Ukraine since end of February. The reality is that it is the western sanctions that are responsible. Those sanctions including cutting SWIFT interbank access for key Russian banks and some of the most severe sanctions ever imposed, are hardly having an impact on the military actions in Ukraine. What many overlook is the fact that they are increasingly impacting the economies of the West, especially the EU and USA. A closer look at the state of the global supply of diesel fuel is alarming. But Western sanctions planners at the US Treasury and the EU know fully well what they are doing. And it bodes ill for the world economy.
While most of us rarely think about diesel fuel as anything other than a pollutant, in fact it is essential to the entire world economy in a way few energy sources are. The director general of Fuels Europe, part of the European Petroleum Refiners Association, stated recently, “… there is a clear link between diesel and GDP, because almost everything that goes into and out of a factory goes using diesel.” … continue
This site is provided as a research and reference tool. Although we make every reasonable effort to ensure that the information and data provided at this site are useful, accurate, and current, we cannot guarantee that the information and data provided here will be error-free. By using this site, you assume all responsibility for and risk arising from your use of and reliance upon the contents of this site.
This site and the information available through it do not, and are not intended to constitute legal advice. Should you require legal advice, you should consult your own attorney.
Nothing within this site or linked to by this site constitutes investment advice or medical advice.
Materials accessible from or added to this site by third parties, such as comments posted, are strictly the responsibility of the third party who added such materials or made them accessible and we neither endorse nor undertake to control, monitor, edit or assume responsibility for any such third-party material.
The posting of stories, commentaries, reports, documents and links (embedded or otherwise) on this site does not in any way, shape or form, implied or otherwise, necessarily express or suggest endorsement or support of any of such posted material or parts therein.
The word “alleged” is deemed to occur before the word “fraud.” Since the rule of law still applies. To peasants, at least.
Fair Use
This site contains copyrighted material the use of which has not always been specifically authorized by the copyright owner. We are making such material available in our efforts to advance understanding of environmental, political, human rights, economic, democracy, scientific, and social justice issues, etc. We believe this constitutes a ‘fair use’ of any such copyrighted material as provided for in section 107 of the US Copyright Law. In accordance with Title 17 U.S.C. Section 107, the material on this site is distributed without profit to those who have expressed a prior interest in receiving the included information for research and educational purposes. For more info go to: http://www.law.cornell.edu/uscode/17/107.shtml. If you wish to use copyrighted material from this site for purposes of your own that go beyond ‘fair use’, you must obtain permission from the copyright owner.
DMCA Contact
This is information for anyone that wishes to challenge our “fair use” of copyrighted material.
If you are a legal copyright holder or a designated agent for such and you believe that content residing on or accessible through our website infringes a copyright and falls outside the boundaries of “Fair Use”, please send a notice of infringement by contacting atheonews@gmail.com.
We will respond and take necessary action immediately.
If notice is given of an alleged copyright violation we will act expeditiously to remove or disable access to the material(s) in question.
All 3rd party material posted on this website is copyright the respective owners / authors. Aletho News makes no claim of copyright on such material.