The coronavirus may go but, from cancer to AIDS, the mRNA vaccines are here to stay.
The Covid19 narrative is broken, that battle is over. Yes, there are still pockets of token resistance, little embattled squares who aren’t ready to give up the ghost just yet, but for the most part the establishment are letting it go.
Country after country after country are “relaxing” their Covid restrictions, abandoning vaccine passport plans and attempting to “get back to normal”.
It seems every week some new “expert” who spent the last two years predicting we’re all gonna die turns up on the news claiming we should “treat Covid like the flu”.
But just because they’re giving slack on Covid does not mean the agenda behind Covid is gone. Far from it.
In fact, even as they seek to dump this pandemic in a shallow grave, they are already prepping the public for the next health scare – AIDs.
In December Joe Biden claimed it was the aim of his administration to “end the HIV/AIDS epidemic by 2030”. A similar campaign, launched in the UK at the same, uses the same exact phrase, word for word.
Then, just last week it was suddenly reported there was a “new variant” of HIV circulating in Europe, this new strain is allegedly “more virulent”, “more transmissable”, and “progresses to AIDS faster”.
At the same time, papers are reporting that for the first time in years heterosexuals are more likely to contract HIV than homosexuals, and they are “more at risk of AIDS” because they’re “diagnosed late”.
On the back of this “news”, a Guardian opinion piece claims we need a “new strategy” for dealing with AIDS.
Following hot on the heels of this fresh wave of fear is a push for everyone to get AIDS tested as soon as possible, from politicians and celebrities and everyone in between.
Prince Harry is leading the charge, in a video that caused the press invoke the spirit of his mother Princess Diana, Harry insisted we all have a “duty” to get HIV tested “to keep other people safe”, comparing it to the COVID outbreak.
“Know your status“, the video says. Which will probably be a hashtag in the near future. (I just checked, and it actually is already.)
They’re really cranking through the gears on this one.
Even while the problem and reaction are still barely out of the research and development stage, they’re already talking about the solution.
Guess what it is?
If you said “another mRNA vaccine”, well done for paying attention
Yes, Moderna has apparently learned so much from making their rushed Covid vaccine which doesn’t work that they’re already making an HIV vaccine they hope will be just as “safe and effective”.
In a truly startling coincidence, Moderna’s HIV vaccine began clinical trials the exact same day the “new variant” of HIV hit the headlines, and the same week as the NHS’s annual “HIV Testing Week”. Funny old world, isn’t it?
Anyway, everyone get ready to line up for the AIDS shot.
Oh, and the cancer one as well.
The covid battle might be slowly winding down, but the mRNA “vaccine” war has potentially only just begun.
February 10, 2022
Posted by aletho |
Deception, Science and Pseudo-Science | HIV/AIDS |
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THE World Health Organisation’s Global Vaccine Action Plan (GVAP) was developed to help GAVI (the Global Alliance for Vaccines and Immunisation) achieve its ‘decade of vaccines’ from 2010, helping ‘all individuals and communities enjoy lives free from vaccine-preventable diseases’.
All countries were to make immunisation a strategic priority, requiring more surveillance to ‘strengthen national capacity to formulate evidence-based policies’. There was no aversion to financially incentivising either individuals or healthcare workers to encourage vaccination, despite the potential for conflict of interest.
The primary success metric in the GVAP was that by 2020 there should be at least 90 per cent national vaccination coverage ‘with at least 80 per cent vaccination coverage in every administrative unit for all vaccines in the national immunisation programme’ for the target populations.
Immunisation Information Systems (IIS), national registries to record the who, what and when of vaccination, were established.
The European Centre for Disease Control (ECDC) led a scoping exercise for this in 2016. Systems which would be interoperable with other databases were to be formulated with ‘a heavy design emphasis on generating evidence to support decisions that need to be made at the population level’.
Vaccination coverage is mentioned 81 times in the ECDC report, twice as many times as vaccine safety. The ECDC claims that ‘IIS can help mitigate potential rumours and unfounded concerns through the provision of evidence, including on adverse events following immunisation’.
That may be so, but the only safety signal likely to emerge from an IIS is evidence of secondary vaccine failure – that is, breakthrough disease outbreaks amongst those inoculated against a given disease, requiring a booster vaccination campaign.
The IIS do not exist for safety monitoring (the technical term for which is pharmacovigilance) of the vaccines once they are deployed on the population at large. Pharmacovigilance is the remit of the regulators who license them, not of the public health authorities who monitor vaccination coverage.
In fact, only seven European countries record adverse events to vaccines in their IIS. The UK is not amongst them. Of the seven that do, only Sweden automatically reports them to the regulator who has the power to withdraw unsafe products from use.
Dr David Sencer is the former director of the US government agency the Centres for Disease Control and Prevention (CDC), who lost his job after America’s ill-fated 1976 swine flu vaccination campaign.
He has pointed out that some adverse effects from vaccines become apparent only once the clinical trials conclude and after the vaccine is administered to very large numbers of people.
Sencer’s swine flu program had an active surveillance system for adverse events which he later called a trojan horse as the scale of death and injury led to the vaccination campaign being terminated after three months. Having indemnified the manufacturers because their insurers balked at covering them, the US government paid $135m for swine flu vaccines and an additional $90m in compensation for death or injury – almost as much in compensation over the swine flu vaccine programme as it did rolling it out.
The size of the US government’s 1976 compensation bill perhaps explains why no pharmaceutical regulator in the world has a system that actively monitors for post authorisation adverse events. Instead all regulators rely on passive surveillance through voluntary reports to systems like the Yellow Card system operated by the Medicines and Health Care Products Regulatory Authority (MHRA) in the UK.
A vaccine is deemed safe if it passes Phase 1 clinical trials without any ‘unscheduled’ animal deaths or untimely deaths of human subjects and effective if it passes Phase 2 clinical trials.
Products such as the ill-fated Pandemrix flu vaccine – hit by adverse effects in 2009 – may on occasion be withdrawn after licensing. But as a rule, regulators make no active effort to protect consumers at large that might necessitate a product being withdrawn once it is in use.
To facilitate GAVI’s efforts to monitor vaccination coverage rates reliably, the GVAP asks for each individual to be assigned a unique identification number so that the respective health authority can ensure everyone gets every vaccine in ‘time-monitored’ adherence with the vaccine schedules.
In 2013, the Bill and Melinda Gates Foundation (BMGF) funded a fingerprint identification system to track vaccinated children in Africa. GAVI, the Rockefeller Foundation and Microsoft subsequently formed the ID2020 alliance in 2016 to promote the global need for secure digital identity.
‘We are currently in the middle of a global identity crisis: Tens of millions of children – especially those living in most remote, impoverished communities – have no formal record of their existence,’ said Dr Seth Berkley, associate director of health sciences at the Rockefeller Foundation, and one of the instigators of GAVI.
‘That represents an enormous impediment to GAVI’s mission of ensuring that every child worldwide receives the essential vaccines they need to survive and thrive.’
He said the pacesetters of GAVI’s initiative called INFUSE (Uptake, Scale and Equity in Immunisation) ‘are on the cutting edge of technologies that might help us overcome that challenge’.
Covid-19 has presented another opportunity to fulfil GAVI’s vaccination monitoring mission. Dr Rebecca Weintraub, a board member of Simprints, one of the companies working with it to develop biometric identification solutions for immunisation registries, said: ‘We have a narrow opportunity to set the stage for such fair and sustainable infrastructure across the globe. If done well, we can ensure the promise of the Covid-19 vaccine portfolio leads to future widespread vaccination – and protection – for global populations.’ https://gatesopenresearch.org/articles/4-182/v2
However, biometric identification for developing immunisation registries is beginning to morph into something else. The Ada Lovelace Institute, which was set up by partners including the Wellcome Trust in 2018 to ‘ensure that data and AI work for people and society’, calls vaccine passports and Covid status apps ‘systems for verifiably sharing private health data relevant to Covid-19 which could be used to stream society and impose differential lockdown restrictions.
‘This might mean limiting individual access to work, insurance, hospitality and leisure, and other parts of life, based on an individual’s health or risk of Covid-19 infection or transmission.’ In other words, universal vaccination means universal control.
Covid-19 may have brought these passports to public attention, but the idea is not new. In December 2017, the European Commission published a Roadmap on Vaccination.
The first action on the roadmap is to ‘examine the feasibility of developing a common vaccination card/passport for EU citizens (that takes into account potentially different national vaccination schedules and) that is compatible with electronic immunisation information systems and recognised for use across borders, without duplicating work at national level.’
In 2018, the European Health Parliament, a lobby organisation that develops health policy recommendations to ‘rethink European health care’ and whose sponsors include Johnson & Johnson and Pfizer, recommended that electronic vaccination passports be established in order to ‘ensure people know and act in their best interests on vaccination’.
The very day the MHRA authorised the use of the Pfizer-BioNTech vaccine, the WHO put out a call for experts to develop a so-called Smart Vaccine Certificate programme.
Pharmaceutical revenue growth has been stimulated not only by measures to increase inoculation coverage, but by raising the number of vaccines put on national immunisation schedules.
The ‘child survival revolution’ promoted by the United Nations agency UNICEF began in 1982 with six vaccines. At the time of the first GAVI board meeting in 1999, there were 11 routinely recommended vaccines on the US national immunisation schedule.
GAVI immediately identified a vaccine gap that the developing world needed to close, and its ambition is for immunisation schedules around the world to mirror that of the US.
The goalposts keep moving. When it was updated again in 2013, the US immunisation schedule comprised a total of 52 injections of 17 different vaccines over the course of a person’s lifetime.
Gone are the days when the promise made to parents was that with a single injection their children could avoid infections and be protected for life. The number of boosters continues to increase and now includes a recommendation for adults to have an additional measles, mumps and rubella (MMR) vaccine.
A footnote to the MMR recommendation says: ‘Documentation of (healthcare) provider-diagnosed disease is not considered acceptable evidence of immunity for measles, mumps or rubella.’
The very idea that someone might have acquired lifelong immunity after recovering from an infectious disease is now anathema, unless proven by a laboratory test.
The current UK immunisation schedule is marginally more conservative, both in terms of the total number of vaccines recommended and the number of doses. The most recently updated version, as of November 23, 2021, appeared on the website of the Oxford Vaccine Knowledge Project.
It recommends only three vaccines for adults – flu, pneumococcal and shingles. The three are recommended by Public Health England only for over-65s, or 70 in the case of the shingles vaccine. Despite the controversial mandate for NHS staff to have the Covid-19 vaccine – now withdrawn – the jab is not listed on the schedule.
The Oxford Vaccine Knowledge Project’s medical information is reviewed by Professor Andrew Pollard, chair of the UK’s Joint Committee on Vaccination and Immunisation, and a member of the WHO’s Scientific Advisory Group of Experts Committee.
February 10, 2022
Posted by aletho |
Civil Liberties, Deception, Science and Pseudo-Science | GAVI |
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The U.S. Food and Drug Administration (FDA) and Centers for Disease Control and Prevention (CDC) did it again.
The FDA last week granted its seal of approval for a ghost vaccine that is unavailable in the United States — and it did so using a preordained process that made a mockery of “science” and of “regulation.”
Days later, the CDC backed the FDA’s decision, using similarly flawed data and reasoning.
The approval of Moderna’s Spikevax COVID-19 vaccine was an even greater travesty than the FDA’s approval last August of Pfizer’s Comirnaty shot.
That’s because Moderna has been even more secretive than Pfizer about its trial data, and because Moderna’s shot is linked to an even higher rate of heart disease than Pfizer’s.
The FDA’s approval of the Pfizer Comirnaty vaccine led people to believe they would get a fully licensed, FDA-approved vaccine — when in fact they were still getting the Pfizer-BioNTech vaccine distributed under Emergency Use Authorization (EUA).
People can ask for the Comirnaty vaccine as often as they like — but it is not being distributed in the U.S. The Comirnaty vaccine is supposed to be the same formulation as the old Pfizer-BioNTech vaccine, but the vials labeled “Comirnaty” are in a legal class of their own.
Why this Kabuki theater?
Because any adult who is harmed or killed as a side effect of an “FDA-approved” vaccine can sue the manufacturer. But if you are harmed in exactly the same way by an EUA vaccine, you are out of luck — the manufacturer and everyone in the chain of delivery has full immunity from lawsuits. The law depends on the label.
Now Moderna has the same legal advantage as Pfizer. Its “Spikevax” is the same formula as the old Moderna vaccine, but only if you are dosed with a vial bearing the “Spikevax” label can you sue for bodily harm. So, of course, the Moderna vaccine continues to be distributed, but Spikevax is not available in the U.S.
The approval of Spikevax is not just a legal sham. It’s also a scientific sham. FDA approval is supposed to include long-term safety testing, but there is no long-term data available for a product that has been in existence less than a year.
The FDA hearings on the licensing of Spikevax were one-sided and dominated by self-congratulatory rhetoric. They also raised more questions than answers.
Questions for the FDA
- Besides offering publicity to the manufacturer and sowing confusion in the public mind, why would the manufacturers want FDA approval for a vaccine that is not available in the U.S.?
- Neither Pfizer nor Moderna explicitly specified the content of their placebos, but a published review claims they were simple saline. If this is the case, why is the rate of medical problems following injection with a “placebo” so much higher with Moderna’s placebo compared to Pfizer’s placebo?
For example, 18 people out of 15,000 in the Moderna placebo group died before the start of the trial (2 weeks from the second vaccination), while only 4 people out of 22,000 who received Pfizer’s placebo dose died in a comparable period. There were 31 “severe adverse events” in the placebo group of the Moderna trial, and zero in the (larger) Pfizer placebo group. What was in that “placebo” that killed 18 people and sent 31 to the hospital?
- The FDA relies on the Vaccines and Related Biological Products Advisory Committee (VRBPAC) to help assess the safety of vaccines before approval. There was an animated debate at the VRBPAC meeting for the Pfizer vaccine. Why was VRBPAC not invited to convene for the Moderna vaccine? The answer is given in this letter of approval from the FDA to Moderna (January 31, 2022):
“We did not refer your application to the Vaccines and Related Biological Products Advisory Committee because our review of information submitted in your BLA [Biologics License Application], including the clinical study design and trial results, did not raise concerns or controversial issues that would have benefited from an advisory committee discussion.”
- The FDA plainly states that it limited the scope of its analysis to the trial data alone. Why isn’t the FDA interested in the enormous amount of data that has become available in the last year?
Safety: Did FDA cook the books?
Deaths and disabilities associated with the mRNA “vaccines” have occurred with shocking frequency, 90 times as many as the worst vaccine in the past. There have been more than 1 million COVID vaccine reactions reported to the Vaccine Adverse Event Reporting System (VAERS), compared to 11,000 for the worst vaccine in 2020 (Shingrix).
There were more than twice as many deaths related to the COVID vaccines this year as the sum total of all vaccine deaths in the 30-year history of VAERS.
To rig the approval process in favor of such a product, the FDA needed to rewrite the rule book. The agency did this with a new statistical criterion, masking murder with mathematics. I am grateful to Matthew Crawford for having decoded the algebra and sounded the alarm.
The safety criterion chosen by the FDA is an obscure computation called PRR, which stands for Proportional Reporting Ratio. As the name implies, it is based on RATIOS of different event types and is utterly blind to the ABSOLUTE RATE of such events.
PRR measures the distribution of different kinds of adverse events, e.g. blood clots, heart attacks and deaths. If those ratios are severely out of line with the great variety of vaccine reactions in the past, PRR would detect that.
For example, if the new vaccines caused an extraordinary risk of myocarditis, but everything else was low, then PRR would flag that. But if myocarditis was just one risk among many that have been reported from past vaccines, then PRR would not pick that up.
The real scandal is that PRR is blind to the absolute risk numbers. PRR is defined in such a way as to look for unusual PATTERNS of adverse events, but it is completely insensitive to unusual RATES of adverse events.
Of course, it is the rates and not the patterns that are of primary concern, and the PRR is designed NOT to reflect that.
For example, suppose we have two vaccines:
- Vaccine A has 1 reported death per million vaccinations, 3 reported heart attacks per million, and 20 reported headaches per million.
- Vaccine B has 1 reported death per hundred vaccinations, 3 reported heart attacks per hundred, and 20 reported headaches per hundred.
Vaccine A is quite safe, and vaccine B is extremely dangerous. And yet the formula for PRR will produce the same result for vaccine A and B!
Clearly, PRR is not an appropriate criterion for evaluating the safety of any particular vaccine. Did the FDA use PRR in order to cook the books?
In Moderna’s own trials, 1.3% of vaccine recipients had a reaction to the vaccine that was severe enough to require medical attention. The following possible side effects were listed in information given to doctors:
“Anaphylaxis and other severe allergic reactions, myocarditis, pericarditis, and syncope have been reported following administration of the Moderna COVID-19 Vaccine during mass vaccination outside of clinical trials.”
Off with his head! — the CDC’s ACIP hearings
In Alice’s Wonderland, the Red Queen’s justice began with the execution, then there was a verdict — and finally a trial.
The FDA hearing was followed by a meeting of the Advisory Committee on Immunization Practices (ACIP), which reports to the CDC.
The committee on Feb. 4 voted to recommend the Moderna Spikevax. Only after that action step had been secured did the committee hear testimony from the Public Health Agency of Canada that Moderna’s vaccine was associated with a myocarditis risk five times higher than Pfizer’s.
Questions for the CDC
- All-cause mortality was equal in both placebo and vaccine groups (16 deaths in each). In the midst of a pandemic, Moderna’s vaccine demonstrated no survival benefit. This should have been enough to end any further consideration of approval.
- We have detailed data on myocarditis from decades of past history. One-fourth of myocarditis patients are dead within 5 years, but the same study reports that if the myocarditis is caused by human immunodeficiency virus, then three-fourths die in the same 5 years.
We have no long-term data on vaccine-induced myocarditis, but we do have some 6-month data, which show 39% of cases still had their activity restricted by their doctors, 20% were still on heart medication, 32% still reported chest pain, 22% still had shortness of breath, 22% had palpitations and 25% still reported fatigue. Thirteen vaccine recipients died. (All these numbers were presented at the ACIP hearing on Feb. 4.)
Why should we have confidence that the course of vaccine-induced myocarditis will be much less severe than other forms of the disease?
- The Moderna trial, like the Pfizer trial, was limited to healthy people, mostly young, with no pre-existing problems. Pregnant women were explicitly excluded. Why is the vaccine being approved as safe for everyone, including diabetics and immune-compromised, elderly and pregnant women?
- When mRNA vaccines were approved on an emergency basis, the FDA promised to track all safety concerns with a new cell phone app called V-Safe. Why are the results of V-Safe being withheld from the public?
- The FDA was considering approval of Moderna’s vaccine in January 2022. There was a full year’s experience with side effects reported from nearly 200 million doses of the Moderna vaccine in the U.S. alone. But the FDA limited its consideration to the 15,000 subjects who were in the Moderna trial, ending March 26, 2021. Why was this huge trove of data on vaccine safety not reviewed by the FDA?
- Yes, we understand that the vaccine doesn’t become fully effective until 2 weeks after the second shot. But is that a reason to exclude from consideration the damage that is inflicted by enhanced vulnerability to disease during those two weeks, or, for that matter, the four weeks between shots? These have been counted as diseases of the “unvaccinated,” but in fact, people in this stage of treatment are much more vulnerable than the truly unvaccinated.
- France and Germany do not recommend Moderna’s vaccination for young people, presumably because the Moderna vaccine is associated with a higher rate of myocarditis than the Pfizer vaccine. How did our FDA come to a different conclusion?
- Anaphylaxis following vaccination is an immediate, life-threatening and an undeniable consequence of the vaccine. The CDC claimed the rate of anaphylaxis is 6 per 1 million.
However, in March of 2021, an examination of anaphylaxis following mRNA vaccines revealed a much higher incidence of this adverse event. In fact, 9 of 38,971 Moderna vaccine recipients suffered documented anaphylaxis. This equates to 230 per million, or 38 times higher than the CDC estimate.
Efficacy — but at what cost?
The proper measure of the efficacy of any medication is how it affects all aspects of a patient’s health. But in evaluating the Moderna vaccine, the FDA looked only at its effect on COVID.
There are early but disturbing indications that vaccination worldwide has had dramatic effects on other aspects of health, unrelated to COVID. Insurance company trade journals report that they are paying life insurance claims for adults 18-64 years of age at a rate 40% higher than during any normal year.
This number from OneAmerica (Indianapolis) has been echoed by other studies in Europe. A leaked spreadsheet from the Defense Medical Epidemiological Database showed that incidences of many medical problems in the U.S. military surged in this year of vaccination. For example, heart attacks were up 343%, cancers up 218%, among many other disorders.
Could it be that the vaccines have had a small benefit for COVID severity and disastrous impact on other aspects of human health?
We now have some real-world experience with the efficacy of vaccines. For example, we know the virus mutated to a more contagious, less lethal form. Omicron is now the dominant form of the virus in the U.S. and most other parts of the world today.
The Omicron mutations are concentrated in the spike protein — the only part of the virus to which the vaccinated population has immunity. This suggests the virus is mutating in response to the vaccine, and mutations are an important factor affecting efficacy in the long run.
Nevertheless, the FDA considered efficacy data predominantly from the first five months of data (through March 26, 2021) in making its decision to fully license Spikevax, with an absolute cutoff in November, before Omicron became dominant.
More questions
- Almost all subjects in the original Moderna trial who received placebo initially were subsequently given the vaccine. How will we ever know the long-term effects of the vaccine if we have no controls with which to compare?
- Why do CDC studies of death rates based on vaccination status differ so markedly from the same question asked by independent groups in other countries?
Here, for example, is a report from Public Health Scotland stating that vaccination increases vulnerability to Omicron. Here is a similar report from England. This study shows countries with higher vaccination rates tend to have higher rates of COVID, and this one confirms the same result for U.S. states.
- We are now in an era dominated by the Omicron variant, against which all the vaccines seem much less effective. But even “follow-up data” was analyzed only through March 26, 2021, nine months before Omicron took over. Why did the FDA base its decision on data only from older variants?
- The secondary efficacy endpoint was the prevention of severe COVID-19. Now that it is accepted that there is little, if any, protective effect of mRNA vaccines from infection, the prevention of severe disease should be the primary focus of approval determination.
Moderna claims its vaccine efficacy is an astonishing 98.2% in preventing severe COVID-19 (Table 8). Pfizer’s was 96.7% (Table S6).
The reason for the calculated difference in efficacy between these two products was not from a lower incidence of severe disease in the vaccine arm of Moderna’s trial (it was lower in Pfizer’s trial). It was because the incidence of severe disease in Moderna’s placebo group was much higher than in Pfizer’s.
Severe COVID-19 in Pfizer’s placebo group occurred in 30 participants out of 23,0379. In Moderna’s, severe disease occurred in 106 participants out of 14,164 that received a placebo. Why was the incidence of severe COVID-19 nearly six times higher in Moderna’s placebo group than Pfizer’s?
Postscript: Failure was never an option
In America, why are clinical trials for new drugs run by the same companies that own the drugs, and will profit from them if the trial is successful?
It’s a glaring conflict of interest, but necessary within a capitalist system. Since the trials cost, typically, hundreds of millions of dollars, only the company that will profit from the drug is motivated to invest such huge sums in testing.
In the case of the COVID vaccines, however, the development and the trials were both publicly funded. There was no excuse for contracting the same organization both to develop and test their own product.
Moderna’s development cost was funded through Operation Warp Speed in the U.S. and Pfizer through the German government. Now, the companies are reaping windfall profits, though they risked no money of their own.
This leaves us wondering, did our government ever want a fair and unbiased evaluation of the COVID vaccines? Or — after a full year of telling the public that vaccines were the only path out of the COVID crisis — did NIH feel they could not risk the possibility that the trials might fail?
There were no animal tests. There was no time to experimentally optimize dosage and delivery. They had to guess right the first time.
Maybe they thought this is what the exigency of a pandemic required — but please don’t call it “science.”
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.
© 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
February 10, 2022
Posted by aletho |
Corruption, Deception, Science and Pseudo-Science, Timeless or most popular | CDC, COVID-19 Vaccine, FDA, United States |
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Defense contractors and program advocates have unusual control over what the public sees, leading to bad oversight, or worse.
Withholding information under the guise of classification “undermine[s] our national security, as well as critical democratic objectives, by impeding our ability to share information in a timely manner,” Director of National Intelligence Avril Haines said just last month. The Wall Street Journal, Senator Elizabeth Warren, and the Washington Post all agree. But the Defense Department is going in the opposite direction. It is attempting to mask deficiencies in weapons programs — revealed by their own testing — from the public.
This effectively squashes debate and oversight of their programs. The costs come in the form of more expense, additional delays, and underperforming weapons in the hands of our military, which has and will cost lives.
Nickolas H. Guertin, the Defense Department’s newly installed Director, Operational Test and Evaluation (DOT&E), wasted no time undermining his own office by going along with a scheme egged on by the military services to bury information about how the weapons they buy with taxpayer money are actually performing. Mr. Guertin endorsed his office’s new FY 2021 Annual Report, required by law, with wholesale deletions of presumably relevant material deemed not classified, but “Controlled Unclassified Information” (CUI), a category created during the Obama administration but not so dramatically exploited in these reports until now.
Last December, Guertin’s immediate predecessor explained that unclassified information was being removed from the new public report because it “shouldn’t wind up in our adversaries’ hands.” Of course any material that will help enemies should be withheld and reported only in the classified version of the Director’s Annual Report to Congress. However, there is an important class of information that is essential to understand the depth and scope of plusses and minuses in how a weapon has performed in testing and how rigorously it was tested. This is essential to public understanding, and it is that comprehension that drives oversight by Congress, and even the Pentagon, to fix the problems. This is how our system attempts to make sure no seriously flawed systems get into the hands of our forces, which would truly aid the enemy, in addition to endangering our own people.
The unclassified-but-not-for-public-eyes information (a preposterous category in itself) is not an effort to keep the enemy in the dark, but to keep the public in the dark. It stems from advocates of programs in the Pentagon bureaucracy and defense contractors seeking to mask deficiencies. They want to make sure no controversies emerge that might endanger the money flow, even when the problems cost more, cause delays, limit the combat effectiveness of these weapons, and endanger the lives of the troops. That is precisely what the DOT&E law was designed to stop when it was created in 1983 by a group of Republicans and Democrats in Congress over the bitter opposition of the Pentagon leadership and fellow travelers in Congress and industry.
Under the new CUI regime, the omissions are serious. Director Guertin’s report discloses that 22 accounts of weapons and their testing saw information removed by the military services. An article from Breaking Defense discusses what has been deleted, such as whether the defense systems on the Navy’s new $13 billion aircraft carrier can or cannot “detect, track, engage, and defeat the types of threats for which the system was designed.” It is one thing to foolishly disclose a technical flaw an enemy can exploit; it is quite another to disclose that system X, Y or Z cannot do its job — and with enough detail to permit an understanding whether the problem is serious and what fixes must be applied. Keeping that information away from the public simply means that Congress and the Pentagon will be under less pressure to act responsibly — and that the pressure that is applied will be less informed and easier to overcome.
Not among the programs that Breaking Defense found to have been watered down by the withholding of unclassified information was the notorious F-35, suggesting there is a second level of information deletion at work here. Reviewing the F-35 report submitted by Director Guertin, compared to predecessors, reveals a fundamental — even profound — problem.
The Annual Report submitted by DOT&E J. Michael Gilmore in his last report in FY 2016 contained 62 pages of analysis of the F-35. Reports by his immediate successor, Robert F. Behler, varied from 30 to 16 pages. The section of the Guertin report on the F-35 is a whole nine pages. The texts of the previous reports were radically different. They contained multiple tables, details, and explanations for how and why the F-35 was failing to meet its performance and reliability thresholds, let alone combat expectations. Under meaningful explanatory discussion were issues such as the inability of the aircraft to be available for a mission, unpredictable performance in a stressful combat environment, and details like un-commanded maneuvers due to aerodynamic flaws and the gun not shooting where the pilot aimed.
Also reported were the efforts of some in the military services and the F-35 Joint Program Office to incompletely test the aircraft or manipulate test results. None of this shows up in the public Guertin report. Multiple issues, such as the gun, have disappeared, and previous manipulations of the hundreds of deficiencies discovered in the F-35 would appear to be less of a concern today.
There are two problems here, not one: there is the information behind the CUI labeling cover, and information never included in the report because the DOT&E office knew what the military services wanted addressed, and what they didn’t. It is the latter —self-censorship — that appears far more serious than the false classification issue. Why? Because it results in not just the deletion of phrases and sentences, but presumably pages and pages of detail and analysis. On the other hand, those with access to the CUI version of the report can make a comparison, should they choose to do so.
Program advocacy in the Pentagon, much of which is done by defense corporations, is exercising control over the previously more independent and objective reports to Congress and the public on weapons testing. Inadequate public reporting means feeble oversight, plain and simple.
The current Director of the Operational Test Office is new to the job, but he is off to a very poor start. His office was created to contend with the forces arrayed against tough testing and complete, honest reporting, not comply with them. If there is any meaningful oversight in Congress, the redactions in DOT&E Guertin’s recent Annual Report should be fully assessed. More importantly, the prior restraint/self-censorship apparent in producing this and any other DOT&E reports needs to be fully investigated and eviscerated.
February 9, 2022
Posted by aletho |
Corruption, Deception, Militarism, Timeless or most popular | Obama, United States |
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If you’ve ever felt like Google’s watching you, it’s because they, quite literally, are. “The truth is that contrary to Google’s representations it continues to systematically surveil customers and profit from customer data,” Karl A. Racine, the attorney general for the District of Columbia, said in a statement.1
He’s among four attorneys general who have sued Google for its deceptive practices in collecting location data from the public. The separate lawsuits allege that Google continued to track location data of its users even after they had disabled location tracking.
“Google falsely led consumers to believe that changing their account and device settings would allow customers to protect their privacy and control what personal data the company could access,” Racine said.2
Google’s Been Secretly Tracking People Since at Least 2014
Racine initiated an investigation into Google after a 2018 AP News report revealed Google was tracking people’s movements even when they’d opted out of such tracking.3 Google’s misleading claims to users regarding privacy protections available in their account settings have been ongoing since at least 2014, Racine’s investigation found.4
The AP investigation included a real-world example from privacy researcher Gunes Acar, whose location was tracked to dozens of locations over the course of several days, and the data saved to his Google account, even though he had turned “Location History” off on his cellphone.5
Location data collected by Google has been used in criminal cases in the past, including a warrant issued by police in Raleigh, North Carolina, to track down devices in the area of a murder.6 When you use an app like Google Maps, it will ask you to allow access to location, but it also tracks your location during use of apps that you might not expect. According to the AP investigation:7
“For example, Google stores a snapshot of where you are when you merely open its Maps app. Automatic daily weather updates on Android phones pinpoint roughly where you are. And some searches that have nothing to do with location, like “chocolate chip cookies,” or “kids science kits,” pinpoint your precise latitude and longitude — accurate to the square foot — and save it to your Google account.
The privacy issue affects some two billion users of devices that run Google’s Android operating software and hundreds of millions of worldwide iPhone users who rely on Google for maps or search.”
Tracking You Even When ‘Location History’ Is Off
At issue is the company’s continued tracking of its users even when Location History is turned off. “If you’re going to allow users to turn off something called ‘Location History,’ then all the places where you maintain location history should be turned off,” Jonathan Mayer, a former chief technologist for the Federal Communications Commission’s enforcement bureau, told the AP. “That seems like a pretty straightforward position to have.”8
Indeed, it states on Google’s Account Help webpage, “You can turn off Location History for your account at any time.” Only lower down on the page does it explain, however, that location data may still be saved even if Location History is paused:9
“If you have other settings like Web & App Activity turned on and you pause Location History or delete location data from Location History, you may still have location data saved in your Google Account as part of your use of other Google sites, apps, and services.
For example, location data may be saved as part of activity on Search and Maps when your Web & App Activity setting is on, and included in your photos depending on your camera app settings.”
Aside from hiding location tracking under settings users wouldn’t expect, like Web & App Activity — which is turned on by default — Google is accused of collecting and storing location information via Google services, Wi-Fi data and marketing partners, again after device or account settings had been changed to stop location tracking.10
In addition to the District of Columbia, the attorneys general of Texas, Washington and Indiana have also filed lawsuits against Google for their deceptive data collection practices. The suits allege that Google also pressured users to use location tracking more often because it claimed — falsely — that its products wouldn’t function properly without it.11
“Google has prioritized profits over people,” Todd Rokita, Indiana attorney general, told The New York Times. “It has prioritized financial earnings over following the law.”12 Texas, meanwhile, has also filed an antitrust lawsuit against Google that alleges it has abused a monopoly over ad space auctions to marketers. The suit joins those from more than a dozen other states that claim Google has maintained and abused a monopoly over searches online.13
Google Is Even Tracking Children
Google has been called a dictator with unprecedented power because it relies on techniques of manipulation that have never existed before in human history, according to Robert Epstein, a Harvard trained psychologist who is now a senior research psychologist for the American Institute of Behavioral Research and Technology, where for the last decade he has helped expose Google’s manipulative and deceptive practices.
They’re not only a surveillance agency — think about products like Google Wallet, Google Docs, Google Drive and YouTube — but also a censoring agency with the ability to restrict or block access to websites across the internet, thus deciding what you can and cannot see.
Google has also infiltrated education with its Google classrooms, usage of which skyrocketed during the pandemic, but many aren’t aware that even their children are being tracked. The attorney general of New Mexico filed a suit against Google for its educational tools in its classroom suite, helping to “break through the fog,” Harvard professor Shoshana Zuboff said:14
“[The suit is] identifying the huge amounts of data that they’re taking about kids, how they track them across the internet are they integrate it with all the other Google streams of information and have it as a foundation for tracking those children all the way through their adulthood.”
The suit was later dismissed, but the attorney general filed an appeal, maintaining that Google’s G-Suite for Education products “spy on New Mexico students’ online activities for its own commercial purposes, without notice to parents and without attempting to obtain parental consent.”15
Google Force Installed COVID-19 Tracking Apps
In another sign of Google’s dictatorial tendencies, it partnered with the Massachusetts Department of Public Health and Apple to create a smartphone app called MassNotify, which tracks and traces people, advising the users of others’ COVID-19 status.
While the tool claims to have been developed “with a focus on privacy,”16 the app suddenly appeared on Massachusetts residents’ Android phones out of nowhere, without consent. The feature must be enabled by the user for it to function, but it’s extremely disconcerting that the tool was automatically added to people’s cellphones, whether they intend to use it or not.
In China, COVID-19 tracking apps have been used as surveillance tools in collaboration with its social credit system, raising red flags that this force-installed app could be tracking residents’ movements and contacts without their knowledge and consent. The MassNotify app uses Google’s and Apple’s Bluetooth-based Exposure Notifications Express program.
The software framework was first released in April 2020,17 with the goal of allowing users who test positive for COVID-19 to report their results, which then sends out an alert to anyone whose phone crossed paths with the positive case and may have been exposed. The Exposure Notifications Express program acts as a blueprint from which states can implement their own tracking systems without having to develop their own individual apps.
While other states have required users to download an app to use the system, MassNotify was integrated directly into the operating system of Android phones.18 Such apps are based on technology developed by Apple and Google that was previously known as the “Privacy-Preserving Contact Tracing Project”19 and is now referred to as the Exposure Notifications API (application programming interface).
In a May 2020 Forbes article by Simon Chandler, he pointed out that while contact tracing apps “may be cryptographically secure,” they still “threaten our privacy in broader and more insidious ways,”20 namely encouraging you to keep your cellphone with you at all times and tracking your whereabouts while you do, and further “normalizing” the constant use of technology to dictate your freedoms and behavior.
Using ‘Trickery for Profits’
The attorneys’ general lawsuits against Google are seeking fines and an end to Google’s use of “dark patterns” that influence users to give up more and more personal data in order for the company to increase its profits. The suits allege that Google’s products are designed to pressure users to allow location tracking “inadvertently or out of frustration,” in violation of state consumer protection laws.21
“Google uses tricks to continuously seek to track a user’s location,” Racine said. “This suit, by four attorneys general, on a bipartisan basis, is an overdue enforcement action against a flagrant violator of privacy and the laws of our states.” The more data that Google collects about individual users, the more advertising dollars it can generate. But, Racine noted, “The time of trickery for profits is over.”22
In a similar lawsuit filed in 2020, Arizona attorney general Mark Brnovich also alleged that Google used deceptive practices to track its users’ locations. That suit stated:23
“This case concerns Google’s widespread and systematic use of deceptive and unfair business practices to obtain information about the location of its users, including its users in Arizona, which Google then exploits to power its lucrative advertising business. Google makes it impractical if not impossible for users to meaningfully opt-out of Google’s collection of location information, should the users seek to do so.”
Location data, meanwhile, can be used to reveal your gym memberships, health care visits, stores and restaurants you frequent or where you go to church. It may also be used to provide personalized ads on digital billboards as you pass by, and Google tracks and provides to its customers information about how well online ads work to drive people into brick-and-mortar stores.24
In addition to disabling as many location tracking apps as possible, and deleting your location history from your Google accounts, you can avoid additional Google products — and the privacy invasions they entail — using the following tips:
- Stop using Google search engines. Alternatives include DuckDuckGo and Startpage
- Uninstall Google Chrome and use Brave or Opera browser instead, available for all computers and mobile devices. From a security perspective, Opera is far superior to Chrome and offers a free VPN service (virtual private network) to further preserve your privacy
- If you have a Gmail account, try a non-Google email service instead such as ProtonMail, an encrypted email service based in Switzerland
- Stop using Google docs. Digital Trends has published an article suggesting a number of alternatives25
- If you’re a student, do not convert the Google accounts you created as a student into personal accounts
Sources and References
February 9, 2022
Posted by aletho |
Civil Liberties, Deception, Full Spectrum Dominance, Timeless or most popular | China, Covid-19, Google, Human rights, United States |
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In Part 5 I look at the scientific literature on face mask use. I look at a lot of studies, but I am not undertaking an exhaustive review of all mask studies, which is an impossible task. However, I do review all the randomized controlled trials, which are the most credible trials. After that I look at a selection of the better trials and meta-analyses. I do focus more on those papers that conclude that there is little or no benefit to mask wearing. I have done this because academia, governments, health institutions and the media are currently giving such an appallingly one-sided view that a corrective is needed.
Also, many of the studies that pro-maskers refer to are not credible, or are not relevant to the real world, and a better evidence base is required.
Bear in mind, as statistician William Briggs says,
The burden of proof is entirely on those who make masklessness a crime: they are imposing, we are not. I have no obligation, none whatsoever, to show masks do not work. But, we have more than enough evidence they do not.
I also refer the reader to City Journal’s ‘Do Masks Work? A Review of the Evidence’, which demolishes some poor studies, including ones that the CDC has pushed. For example, the CDC has especially promoted an incredibly weak observational study which
focused on two Covid-positive hairstylists at a beauty salon in Missouri. The two stylists, who were masked, provided services for 139 people, who were mostly masked, for several days after developing Covid-19 symptoms. The 67 customers who subsequently chose to get tested for the coronavirus tested negative, and none of the 72 others reported symptoms.
The CDC’s spin was reported uncritically in media such as the New York Times.
‘This study’, the City Journal article went on,
has major limitations. For starters, any number of the 72 untested customers could have had Covid-19 but been asymptomatic, or else had symptoms that they chose not to report to the Greene County Health Department, the entity doing the asking. The apparent lack of spread of Covid-19 could have been a result of good ventilation, good hand hygiene, minimal coughing by the stylists, or the fact that stylists generally, as the researchers note, “cut hair while clients are facing away from them.” The researchers also observe that “viral shedding” of the coronavirus “is at its highest during the 2 to 3 days before symptom onset.” Yet no customers who saw the stylists when they were at their most contagious were tested for Covid-19 or asked about symptoms. Most importantly, this study does not have a control group. Nobody has any idea how many people, if any, would have been infected had no masks been worn in the salon. Late last year, at a gym in Virginia in which people apparently did not wear masks most of the time, a trainer tested positive for the coronavirus. As CNN reported, the gym contacted everyone whom the trainer had coached before getting sick—50 members in all—“but not one member developed symptoms.” Clearly, this doesn’t prove that not wearing masks prevents transmission.
5.1: The effectiveness of face masks: Randomized-controlled trials
5.2: The effectiveness of face masks: Other trials and studies
5.3: The effectiveness of face masks: reviews and meta-analyses
5.4: The effectiveness of face masks: preprints, commentaries, editorials and academic letters
5.5: The effectiveness of respirators in healthcare settings
5.6: The effectiveness of surgical face masks in surgical settings
5.7: Face mask harms
5.8. Relevant media reports (a small selection)
The main Face Mask FAQs page.
February 9, 2022
Posted by aletho |
Deception, Fake News, Mainstream Media, Warmongering, Science and Pseudo-Science, Timeless or most popular | CDC, Covid-19, Human rights, New York Times |
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Yesterday, a number of important Democratic governors lifted mask mandates in their states. Almost to a one, they cited the changes wrought by the fast moving and relatively mild omicron variant of the SARS-CV2 virus as the prime reason for the change.
What none of them did was admit what “the Science” has shown for at least two decades, and has been clear through the last two years to anyone doing a modicum of independent research on the subject: masks have never been shown to fundamentally alter the spread of respiratory viruses within the general population.
What they did say almost to a one, like their counterparts in Great Britain, Denmark and other countries now dismantling previous Covid restrictions, was that the return to normality was greatly facilitated by the uptake of vaccines in the populations they currently govern.
Nearly a half century ago, a man named Ron Ziegler held the position now occupied by Jen Psaki. Like all presidential spokespeople before and since he was a serial dissembler.
But back then there were still a few journalists at the presidential court and beyond willing to do their jobs. And when one day in the midst of the Watergate scandal he used the passive voice construction “mistakes were made” in an attempt to explain away obvious breaches of honesty and ethics committed quite actively by the Nixon Administration, he was roundly mocked by the press corps.
Sadly, however, as I have argued elsewhere, this type of non-apology apology, which caused a scandal then, has become ubiquitous across our social landscape. And that’s a shame.
Why?
Because real apologies and expressions of accountability are important. Without them, neither the apologizer nor the aggrieved party ever experiences what the ancient Greeks considered a cardinal element in human development and human relations: catharsis.
This is especially so in the case of government entities. Without admissions of guilt, the assumptions and premises undergirding failed policies remain intact, lying fallow until such time as the government entity in question feels it opportune to deploy them again in the service of another misguided crusade.
This is what is currently occurring with the Covid hawks who have violated our fundamental rights time and again over the last two years.
These enemies of human dignity and freedom now realize that many of their former supporters among the citizenry feel exhausted, and in many cases, flat out deceived.
At the same time, however, they do not want to permanently relinquish the powerful repressive tools they have acquired during the two-year state of exception.
The answer?
One part of it, already mentioned, is the moderated limited hangout operation now being conducted regarding the use of masks in public. By relaxing these strictures while in no way addressing the fundamental fallacies upon which the masking policies were based, they ensure that mask mandates can be brought back when and if they deem it necessary to do so.
The second part, which is far more pernicious and consequential, is the effort to push a proposition that is at best quite tenuous in light of what actual scientific studies are currently revealing about vaccine efficacy: that without widespread injection uptake the virus would have never receded, and we would have thus never have gotten into a position to recover our freedoms.
Note the underlying logic here. We are not getting our freedoms back because they intrinsically belong to us and were unjustly stolen. We are getting them back because an important plurality of us have done what the “experts” and the “authorities” coerced us into doing.
With this approach there is no catharsis or healing, and certainly no acquisition of new wisdom and knowledge. What there is, is a sly reification of the infantilizing and anti-democratic ways of thinking that have predominated in our policy-making class throughout the pandemic.
Though many people, laboring under the mortal fear of being branded with the weaponized term of “conspiracy theorist,” are reluctant to admit it, the central concern of policy-makers throughout the pandemic has not been the health of our communities, but rather gaining enhanced control over where we go and what we put into our bodies.
There is nothing more central to the idea and practice of freedom than bodily autonomy. It is the basal freedom from which all others are derived. Without it—as the history of slavery starkly reminds us—all other liberties are comparatively ornamental.
For this reason, we must vigorously oppose this organized attempt to present the vaccines, which have been delivered to millions under rather severe coercion, as a great, if not the greatest, hero of the pandemic film.
Thomas Harrington, Senior Scholar at the Brownstone Institute, is an essayist and Professor Emeritus of Hispanic Studies at Trinity College in Hartford (USA) where he taught for 24 years. He specializes in Iberian movements of national identity Contemporary Catalan culture. His writings are at Thomassharrington.com.
February 9, 2022
Posted by aletho |
Civil Liberties, Deception, Science and Pseudo-Science, Timeless or most popular | Covid-19, COVID-19 Vaccine, Human rights, United States |
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An investigation into eight attacks attributed to the loyalist Ulster Defence Association (UDA) or the Ulster Freedom Fighters (UFF) has identified “significant failures” by UK authorities during the period known as The Troubles in Northern Ireland in the 1990s.
Laying out the findings in the 344-page report, published on Tuesday, Marie Anderson, the police ombudsman for Northern Ireland, claimed she was “deeply concerned” by the findings, which showed members of the police force, the Royal Ulster Constabulary (RUC), had deliberately destroyed files.
The “damning” investigation, which found “undiluted evidence of the policy of collusion,” stated that “11 murdered citizens and their families were systemically failed by the British state in life and in death.”
A spike in violence from loyalist paramilitary groups during the Troubles saw the RUC seek to expand its network of informants within the UDA and UFF. The RUC was condemned for a “totally unacceptable” practice of using informants who “were actively participating in serious criminality” and, in some cases, murders. However, the report did not find evidence that police had been handed information that could have stopped the attacks.
The Troubles, which lasted from the 1960s to the late 1990s, saw violent attacks and reprisals between Irish republican paramilitaries and Ulster loyalist groups. The UDA, which had tens of thousands of members at one point, has been deemed responsible for killing hundreds of people during the conflict. It was formally banned in August 1992, and announced in 2007 that “the war is over.” However, in 2018, then-Police Service of Northern Ireland Chief Constable George Hamilton claimed members of the UDA were still involved in criminal activities.
“Areas of the report make uncomfortable reading and I want to offer my sincere apologies to the families of those killed and injured for the failings identified in this report,” PSNI Temporary Assistant Chief Constable Jonathan Roberts said in a statement.
In his remarks, Roberts acknowledged the “continuing distress being felt by all of the families of those killed and injured in these attacks, and want to acknowledge the pain and suffering that they all continue to feel.”
February 8, 2022
Posted by aletho |
Civil Liberties, Deception, Timeless or most popular, War Crimes | Human rights, UK |
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Johnson & Johnson has been accused of trying to suppress speech by asking a judge to block the Reuters news agency from publishing a story about the pharmaceutical giant’s legal strategy to counter lawsuits claiming that its Baby Powder is a cause of cancer.
“The First Amendment is not a license to knowingly violate the law,” J&J said in a court filing in New Jersey this week.
The filing was made at the US Bankruptcy Court where the Big Pharma giant is trying to get protections from “bankruptcy” from 38,000 lawsuits alleging the company’s baby powder product was advertised as safe but had long-term cancer risks.
This week, Reuters reported that J&J had a secret plan to shift the liability from the lawsuits to a new subsidiary which would then declare bankruptcy to limit having to pay up over the cancer lawsuits.
J&J attempted to stop Reuters from publishing the story by requesting the judge intervene and issue a restraining order.
See the court filing here.
J&J accused Reuters of obtaining documents that were protected from public disclosure, demanding that Reuters return the documents and not publish any information.
The request asks for an order:
“(1) precluding the Reuters news agency from using or relying upon any documents designated as “Confidential” in this proceeding;
(2) requiring the return of any such documents; and
(3) ordering each attorney who has made an appearance in the above-captioned proceeding to submit to the Court a declaration under penalty of perjury stating whether he or she disclosed any materials designated as “Confidential” in this proceeding to Reuters (the “Motion”).”
Lawyers for Reuters, in a court filing, said that Johnson and Johnson’s request to stop the publication was “among the most extraordinary remedies a litigant can request under the law” and that the request was a “prior restraint of speech on a matter of public interest.”
After Reuters published its story, J&J withdrew their request for an immediate hearing but was “not prepared to agree” that the request about the documents was moot.
February 7, 2022
Posted by aletho |
Deception, Full Spectrum Dominance | Johnson & Johnson, United States |
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A federal judge Wednesday rejected a bid by the U.S. Food and Drug Administration (FDA), with the support of Pfizer, to delay the court-ordered release of nearly 400,000 pages of documents pertaining to the approval of Pfizer’s COVID vaccine.
Federal judge Mark Pittman of the U.S. District Court for the Northern District of Texas, in an order issued Feb. 2, said the FDA must release redacted versions of the documents in question according to the following disclosure schedule:
- 10,000 pages apiece, due on or before March 1 and April 1, 2022.
- 80,000 pages apiece, to be produced on or before May 2, June 1 and July 1, 2022.
- 70,000 pages to be produced on or before Aug. 1, 2022.
- 55,000 pages per month, on or before the first business day of each month thereafter, until the release of the documents has been completed.
The order grants the FDA the ability to “bank” excess pages as part of this release schedule — meaning that if the agency exceeds its monthly quota in any given month it can apply those extra pages to a subsequent month.
Last week’s ruling is the most recent development in an ongoing court case that began with a Freedom of Information Act (FOIA) request filed in August 2021 by Public Health and Medical Professionals for Transparency (PHMPT), a group of doctors and public health professionals.
PHMPT, a group of more than 30 medical and public health professionals and scientists from institutions such as Harvard, Yale, and UCLA, in September 2021 filed a lawsuit against the FDA after the agency denied its original FOIA request.
In that request, PHMPT asked the FDA to release “all data and information for the Pfizer vaccine,” including safety and effectiveness data, adverse reaction reports, and a list of active and inactive ingredients.
The FDA argued it didn’t have enough staff to process the redaction and release of hundreds of thousands of pages of documents, claiming it could process only 500 pages per month.
This would have meant the cache of documents would not be fully released for approximately 75 years.
In his Jan. 6 order, Pittmann rejected the FDA’s claim and instead required the agency to release 12,000 pages of documents by Jan. 31 and an additional 55,000 pages per month thereafter.
Pfizer responded, to the Jan. 6 order by filing a memorandum with the court on Jan. 21, requesting to intervene in the case for the “limited purpose of ensuring that information exempt from disclosure under FOIA is adequately protected as FDA complies with this Court’s order.”
Pfizer claimed to support the disclosure of the documents, but asked to intervene in the case to ensure that information legally exempt from disclosure will not be “disclosed inappropriately.”
As reported by The Defender, this request, if granted, would have also meant further delay for the release of the next tranche of documents, until May 1.
Lawyers for PHMPT, in a brief submitted Jan. 25, asked Pittman to reject Pfizer’s motion, prompting Pittman’s Feb. 2 order.
The first batch of documents produced in Nov. 2021, which totaled a mere 500 pages, revealed there were more than 1,200 vaccine-related deaths within the first 90 days following the release of the Pfizer-BioNTech COVID vaccine.
Michael Nevradakis, Ph.D., is an independent journalist and researcher based in Athens, Greece.
© [Article Date] Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
February 7, 2022
Posted by aletho |
Deception, Science and Pseudo-Science | COVID-19 Vaccine, FDA, United States |
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You can support the truckers at TruckerLawyer.ca.
As of this writing, I’m told the police are making arrests in Ottawa. I assume this means they’re arresting truckers.
The Ottawa city government has declared a state of emergency. It’s now a crime for anyone on the scene to give food, fuel, or aid of any kind to the truckers.
The truckers and people all over Canada want freedom and peace. The government wants peace without freedom.
The government wants vaccine mandates and passports, and the ability to declare lockdowns and other fascist measures at any time.
No debate on “the science,” no need to justify the COVID measures, no legal cases taking up Constitutional limits on government power. Just: OBEY.
So that’s what the government is. That’s who they are. That’s who Trudeau is.
We might feel shock at what the government is doing to the truckers, but we shouldn’t be surprised. No one should have expected the government of “obey us” to just sit back and let this convoy happen and proceed, with so many Canadians supporting it.
No one should be surprised that rebellion against “obey us” governments is breaking out across the world.
Let’s get out ahead of what could happen in the coming days and weeks—-
No one with a conscience should back away if governments and their media front men throw around words like “insurrection” and “incitement” and “terrorism.” THESE ARE CONTROL WORDS.
They’re meant to paralyze people. They’re crude smears. The implication would be, anyone who is “a trucker” or a “supporter” wants to overthrow the entire government—rather than replace the fascists.
“Overthrow” was the official characterization of the January 6 Capitol break-in, in the US. “Well, led by a guy wearing a helmet and horns, a mob was going to take over the Congress.”
I see. Sure. And Trump, wearing a military uniform, having gained control over the PENTAGON, was going to swagger into the Capitol, declare martial law, and run the US with his junta.
Thereafter, The Rebels, commanded by a cigar-smoking fatigues-wearing Tony Fauci, encamped in the Catskills, would valiantly try to win back The Republic and the Constitution.
The truckers want freedom and peace, and their own right to earn a living. The Canadian government wants peace without freedom for everyone, and they’re ready to use force to force the peace.
If serious violence breaks out in Ottawa, the government will be behind it.
Violence shouldn’t make people back away from supporting the truckers.
Perhaps you noticed that the George Floyd protests and riots and the looting and burning and violence in many US cities didn’t make anyone on the political Left back away from supporting the rioters.
Did the government call those supporters insurrectionists or terrorists?
You might hear this from people “who are really in the know”: “You see, the whole convoy was a PLAN to cause violence, and then anyone who’s against the mandates and supports the truckers would be labeled a terrorist…”
Without real evidence, that formulation could be used to reject ANY form of mass protest on ANY issue. You may as well say ALL OF LIFE IS A FALSE FLAG, and therefore, we should do nothing and support nothing.
If serious violence does break out in Ottawa, a typical shaming operation will launch: “You people who supported the truckers—you’re responsible for this. You thought the truckers were honorable. But they were always breaking the law. They were stirred up by a mob mentality, by you who won’t accept the reality of the pandemic and what we all have to do to return to normal life…”
Guilt by association, except it turns out the people we’re associated with—the truckers—did nothing wrong.
Again, if anyone has actual evidence to the contrary, evidence that shows there was a plan to launch a convoy that would dead-end in violence, and cause the world to shake its head and say, “THIS is what the protesters and the anti-vaxxers were about all along, they’re all crazy…”, then present that evidence.
I say this, because in the coming days, we could see and hear more of such talk.
What I see in this convoy is honor, justice, the struggle for freedom.
Remember: The convoy is a hell of a lot more than the truckers.
It’s all the Canadians who are supporting it. So if a trucker is there simply because he wants to make a living, but he can’t cross the border unless he shows a vaccine passport, and he doesn’t want to take the vaccine, and that’s the sum of his protest; fine.
And if some trucker turns out to be bad actor, so what?
GET OUT AHEAD OF ALL THIS.
Get all these things straight in your mind, because if the presence of many people and trucks in Ottawa endures, you’re going to be WORKED by some experienced PR pros; worked to change your thoughts and opinions and feelings.
That’s their job. That’s how they operate.
Stand firm. Stay strong.
Make your voice heard.
Violence is always a government’s hole card. They play it, and then they say the rebels caused it or made it necessary. They splash the violence on the news, because they know it scares many people, who then retreat.
Don’t retreat.
Violence serves another purpose. People want it to stop, so they look to the current political leadership to stop it. They join forces with the fascists who started or triggered the violence.
Don’t fall for that.
If among all the truckers, there are a few bad actors who are government agents, and they do initiate violence, the news will highlight them to the max. This is pure Orwell 1984 stuff. Put pictures of the faces of “the killers” on the screen, over and over, with anchor voiceover telling the public what to see and think and feel. With the goal of stimulating outrage.
Outrage against everyone who supports the truckers or won’t take the vaccine or is opposed to the mandates.
Don’t buy that op.
Stay strong. Stand firm.
Remember what this is. A fight for freedom.
Here’s something else that could happen. The government suddenly announces a new wave of COVID cases. And the blame is directed at the throngs of unmasked truckers and their supporters out in the streets. Super-spreaders. The news, of course, would play that up. By accusation and indirect suggestion, the public will be told THIS IS EXACTLY WHAT THE PUBLIC HEALTH OFFICIALS FEARED.
The unmonitored numbers of irresponsible persons rebelling against common sense are responsible for KILLING ordinary law-abiding citizens.
That’s a straight con. During the past two years, it’s been played many times.
Don’t be fooled. Case numbers can be rigged at the drop of a hat. That’s been going on since the beginning of the “pandemic.”
Stand firm.
The pandemic story was planned with the sole purpose of canceling freedom.
Yours, mine, everybody’s.
Don’t give in.
Don’t allow yourself to be manipulated.
No matter what.
One more suggestion. Play out, in your mind, a worst-case scenario: The convoy WAS planned by bad actors with the intent to discredit actual freedom fighters and people who refuse the vaccine and oppose the COVID mandates and restrictions. Go ahead. Make a mind-movie of that.
Where does that lead you? What’s the bottom line?
It’s SO WHAT?
Because all the people on the streets and in the trucks ARE for freedom; and if the outcome is planned government-caused violence, that means NOTHING about what we’re fighting for. That discredits NOTHING.
If we stay strong.
If we stand up.
If we make our voices heard.
I could write 10,000 more words about a parallel event to the convoy, but I’ll keep it short. The parallel event was the January 6 rally in Washington after the Presidential election, the rally that had nothing to do with the Capitol break-in. Where hundreds of thousands of people gathered.
There were a number of ideas in the minds of all those people: a stolen election; freedom from lockdowns and other fascist COVID restrictions; opposition to the vaccine; opposition to the self-appointed thought-police of America…
In my opinion, Trump didn’t deserve that massive show of loyalty. Not at all. I’ve explained why in other articles. But the people who were there—they were the important ones. Regardless of who planned the break-in and for what reasons. THEY, the hundreds of thousands, wanted freedom. And still do.
The US government is trying to figure out every possible way to discredit and cancel them. Now.
This is the bigger picture.
Keep your eye on it.
I know. I’m not supposed to bring up the January 6 rally. People who want freedom are supposed to forget that. Hush hush. Because THAT event has been slammed mercilessly and discredited and made into a foul horror show.
But I don’t care. All over the world, the same pattern has been repeating. The people who want to live out in the open and throw off their chains are being painted as criminals. For whatever reasons can be cooked up.
And no, not all protests are the same or are launched for exactly the same reasons. But at the core, the impulse and the foundation are there: WE’RE TAKING IT BACK. FREEDOM.
This isn’t Qanon crap or Trumpism or racism or craziness or any hustle.
This is real.
The big smear, guilt by association, and all the other ops aren’t going to fool us.
If we don’t back down.
If we stand firm.
If we don’t quit.
If we make our voices heard.
No matter what.
Jon Rappoport is the author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX.
February 7, 2022
Posted by aletho |
Civil Liberties, Deception, Solidarity and Activism | Canada, Covid-19, COVID-19 Vaccine, Human rights, United States |
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THOUGH I ask this question as a layman, it hardly seems an unreasonable one. It is this:
What exactly is causing the increased risk of infection following vaccination, evidence of which was reported in the Daily Sceptic last week?
From the most recently published UKHSA Vaccine Surveillance Report data for those who are triple-jabbed and from other NHS data published on the double jabbed, the Daily Sceptic have been able to establish the infection rates by vaccination status as well as the unadjusted vaccine effectiveness for infection for those having two or three doses. The conclusion they reached is that the infection rates continue to be considerably worse in the vaccinated, both double and triple jabbed, which translates into what they describe as ‘highly negative unadjusted vaccine effectiveness estimates’. (My italics)
Their report emphasises that these figures are of rates per 100,000 and therefore already take into account the different sizes of the cohorts, meaning that their finding is not because there are more vaccinated people than unvaccinated in the population, and that factor is taken fully into account. You can read the full analysis here.
It is not just this report – which confirms the daily anecdotal evidence I am in receipt of about people I know to be double or triple vaccinated going down with Covid, especially since the booster was rolled out so determinedly – there also are the reports of surging cases in some of the most vaccinated of countries, most notably Israel. Much as Jacob Rees-Mogg and the Guardian, amongst others, really want to believe that it is unvaccinated who are commandeering all the available ventilators, this is not the case as Will Jones has previously laid bare.
On Saturday Dr Jones reported on the recent dramatic statement of one Professor Yaakov Jerris, the director of a coronavirus ward in an Israeli hospital, who has said that between 70 and 80 per cent of the serious cases in his hospital are fully vaccinated and how the vaccine has ‘no significance regarding severe illness’.
All of which brings me to the question of a phenomenon called Antibody Dependent Enhancement which I first heard of when Mike Yeadon warned about it last April under questioning from James Delingpole.
The term refers to the possibility that the vaccine-induced antibodies in the body somehow augment (rather than mitigate against) the infection when you actually catch it, or if these original antibodies don’t make the infection worse, subsequent booster jabs may well.
Could this be the reason for the spate of covid infection and illness? Could it even be the reason for the shocking surge in post-vaccine illnesses that Neville Hodgkinson reported here last week.
If so, was this a risk that the gene therapy vaccine researchers and producers were aware of?
All of which makes the battle over the FDA’s release of all documents related to the licensing of Pfizer’s Comirnaty COVID vaccine of all the more moment and importance. Their desire to keep their files secret for 75 years raises the question of what it is that they do not want us to know.
February 7, 2022
Posted by aletho |
Deception, Timeless or most popular, War Crimes | COVID-19 Vaccine |
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