Role of supplementation is unclear. Prospectively study Associations, vitamin D supplementation and incident dementia N = 12,388 dementia-free people (from the National Alzheimer’s Coordinating Center)
Methods Baseline exposure to vitamin D was considered D+ No exposure prior to dementia onset was considered D− MCI and depression were both more frequent in the D− group, compared to D+ People taking vitamin D had less MCI and less depression
Adjusted for age, sex, education, race, cognitive diagnosis, depression, and apolipoprotein E (APOE) ε4. Potential interactions between exposure and model covariates were explored. Results Across all formulations, vitamin D exposure was associated with significantly longer dementia-free survival, and lower dementia incidence rate than no exposure
Hazard ratio = 0.60 (95% confidence interval: 0.55–0.65) Vitamin D exposure was associated with 40% lower dementia incidence versus no exposure. Over 10 year follow up of 12,388 2,696 participants progressed to dementia
Among them the 2,696 2,017 (74.8%) had no exposure to vitamin D 679 (25.2%) had baseline exposure
Exposure to vitamin D was associated with significantly higher dementia-free survival 5-year survival for D− was 68.4% 5-year survival for D+ was 83.6%
The effect of vitamin D on incidence rate differed significantly, Vitamin D effects were significantly greater in females versus males
Vitamin D effects were significantly greater in normal cognition versus mild cognitive impairment.
Vitamin D effects were significantly greater in apolipoprotein E ε4 non-carriers versus carriers.
Vitamin D effects were less significantly apolipoprotein E ε4 carriers. (25% one copy, 3% two copies)
Vitamin D has potential for dementia prevention, especially in the high-risk strata.
Vitamin D is known to participate in the clearance of amyloid beta (Aβ) aggregates, one of the hallmarks of Alzheimer’s disease (AD), and may provide neuroprotection against Aβ-induced tau hyperphosphorylation (neurofibrillary tangles) Cholecalciferol may be more effective than ergocalciferol
Recently, we have been touching on this theme of ivermectin as a treatment for cancer. So I was delighted to receive an excellent, well-researched piece on precisely this topic from an esteemed colleague. Dr Gérard Maudrux is a urology surgeon based in France and a strident champion for ivermectin. His article gives good insight into ivermectin’s mechanisms of action, while also acknowledging we have yet to discover them all.
I asked if I could share his article with you, and he graciously agreed. If you would like to read the original – in French – you can do so on Dr Maudrux’s blog.
Ivermectin and cancer: reserved for horses?
Dr Gérard Maudrux
Ivermectin is an extraordinary molecule, given its range of actions and safety. Since its discovery it has saved millions of lives, yet health authorities have relegated it to the status of a treatment reserved for horses; this is because medicines which are in the public domain threaten the pharmaceutical industry.
Here is a testimony received from a blog reader eight days ago:
“My wife is coming out of chemotherapy for advanced stage 3 ovarian cancer (the origin of my wife’s cancer is a mutation in the BRCA2 gene); after being assessed in the United States, she was treated with Taxol and Carboplatin.
Having read studies on the PNAS site (NB: Journal of the American Academy of Sciences ), that IVM associated with Taxol gave amplified results, I decided to supplement the chemo with 12mg of IVM every other day.
The first scan in July showed a large tumour and damage to the peritoneum. Laparoscopy confirmed the diagnosis. Ca125 marker assay = 288. From the start, I told my wife that COVID was still dragging on and that it would be useful to take ivermectin again, which had protected us from the epidemic, but which we had stopped taking in January.
After 3 chemo sessions (9 weeks), a new scan showed that the tumour was in strong regression with almost no trace on the peritoneum. Surgeon’s comment: it’s remarkable, I didn’t expect that. Ca125 dropped to 22! Operation decision within 15 days.
Uterus and ovaries were removed. Surgeon’s comment: this is extraordinary. No tumour, some dead cells on the peritoneum that I removed. The biopsy confirmed that everything has gone, Ca125 at 3.
The oncologist qualified the result as exceptional but that microscopic cells may remain, and so continued the chemo with Avastin from the 5th session. If I understand correctly, this treatment is to prevent the tumour from generating vessels to feed cancerous cells!!!! What tumour?
I informed them of my complementary “treatment” and shared my sources. Studies have shown that ivermectin restores apoptosis – this was of little interest: “I will look into it”. To this day I’m not sure they’ve done any research.”
Take note: this does not mean that ivermectin necessarily influenced this outcome – it may be a coincidence. Nevertheless this case should stand out, because this cancer is very nasty: peritoneal metastases indicate a very virulent and terminal cancer, with 87% mortality when at this stage, giving little hope.
Unfortunately, medicine as practiced in the 21st century gives this observation no value; it is not a randomized study at the cost of a few million. Moreover, no one will invest, since this molecule, which has fallen into the public domain, cannot be profitable. Observational medicine, which seeks to reproduce a possible discovery, no longer belongs in a world where industrialists and biostatisticians have replaced doctors.
It’s a shame, because ivermectin may have potential for actions that have not yet been explored. Besides its action on almost all parasites, its antiviral action proven by veterinarians and covered up in humans, its anti-inflammatory, immuno-regulatory, anti-cytokine shock action, but also its anti hemagglutination action that can protect against certain vascular side effects of vaccination, it is also clearly an adjuvant that reinforces certain anti-cancer treatments. I have also recently concluded that it is an anti-cancer treatment in its own right. It deserves twice its Nobel Prize.
Veterinarians are more advanced than doctors when it comes to the anti-cancer potential of ivermectin. This article from 2019, notes that ivermectin is more than an adjuvant, it is anti-carcinogenic, inhibiting the growth of mammary tumours in dogs – the most common kind in female dogs and with a poor prognosis. This is both in vitro and in vivo, stopping the growth of tumour cells.
This husband’s curiosity may have saved his wife’s life. It’s a shame that doctors are so unaware: this potential of ivermectin is not a recent discovery. But the authorities have done everything to belittle this extraordinary molecule because it is unprofitable.
In 2017, Santé Log and Top Santé covered a PNAS article referring to a study from the University of Osaka, reporting the anti-tumour effect of ivermectin on cancer cells of epithelial ovarian cancer, interacting with the KPNB1 gene responsible for the disease, with a direct effect on tumour apoptosis (programmed cell death which is the process by which cells trigger their self-destruction in response to a signal). Indeed, the KPNB1 gene behaves like an oncogene and the researchers confirm that its overexpression significantly accelerates the proliferation and survival of tumour cells, while its inhibition induces their apoptosis.
Ivermectin inhibits the activity of KPNB1 and has a synergistic effect combined with paclitaxel (Taxol), a standard drug for the treatment of epithelial ovarian cancer. The authors conclude: “we found that the combination of ivermectin and paclitaxel produces a stronger anti-tumour effect on EOC both in vitro and in vivo than either drug alone.” Taxol is also used in certain bronchopulmonary and breast cancers and in Kaposi’s sarcomas associated with AIDS. The synergy with ivermectin seen in ovarian cancer may be equally beneficial elsewhere.
This article in Pharmacologic Research studies the different mechanisms of action of ivermectin in different cancers, based on 114 studies. It states that “Ivermectin has powerful antitumor effects, including the inhibition of proliferation, metastasis, and angiogenic activity, in a variety of cancer cells…. ivermectin induces programmed cancer cell death, including apoptosis, autophagy and pyroptosis… ivermectin can also inhibit tumour stem cells and reverse multidrug resistance and exerts the optimal effect when used in combination with other chemotherapy drugs.”
They note this apoptosis with cells of ovarian cancer, colorectal, kidney, glioblastoma and leukaemia. Autophagy affects glioma, lung cancer and melanoma, and pyroptosis affects lung cancer cells.
Other articles study the action of ivermectin in colorectal and prostate cancer. Studies are underway for an injectable form of ivermectin, on breast, lung, bladder and melanoma cancers. Another notable work is a 2021 book on the repurposing of old molecules. The chapter on ivermectin recounts a number of experiments carried out on all these cancers.
Besides these potential effects on cancers, let’s not forget this other discovery from five years ago: remyelination, opening up avenues in the treatment of multiple sclerosis (here and here). Ivermectin has not finished surprising us.
Unfortunately for all of these applications, we will not see studies that lead to marketing authorization. Indeed, what is ivermectin at a dollar a tablet worth compared to treatments at a few thousand euros promoted by the major pharmaceutical groups?
As for medics who would prescribe this drug, knowing there are no harmful side effects even in the case of it not working, they will nevertheless be prosecuted. Rules are rules, it seems, and patients’ wellbeing is secondary.
Medicine is not moving in the right direction. Doctors don’t tend to like patients coming and asking for this or that examination or treatment, because they “saw it on the internet”. But if the doctors have thrown in the towel, surely this means someone else has to step up to the plate? It was not this husband’s job to read the medical articles that doctors should have read, but he was right to do so. I can’t help but liken this to reports of vaccine-related adverse events. In pharmacovigilance records, there are almost as many withheld statements made by patients as by health professionals.
It is not the role of patients and families to research treatments and report on their findings, but that of health professionals, many of whom seem to be AWOL. If we continue like this, in future it will be the patients treating the health providers! In the meantime, at least the horses will be well cared for.
I am frequently asked: why are the government agencies still pushing COVID-19 vaccination after there have been calls in the US Senate and all around the world to pull them off the market for lack of safety and efficacy?
In a March 10, 2023 letter from FDA Commissioner Robert Califf, MD, and CDC Director Rochelle Walensky, MD, MPH, to Florida Surgeon General Joseph Ladapo, MD, PhD, the agencies give their rationale. While Walensky does not have a compelling academic track record, her FDA counterpart Califf has been considered a staunch advocate of randomized trials and a hawk on safety of cardiovascular drugs over his career which was notable for building the Duke Clinical Research Institute, one of the most impressive academic research organizations in the world.
Here are 10 assertions that Califf and Walensky make to Ladapo and Americans on why the COVID-19 vaccines should be “pushed.”
“The claim that the increase of VAERS reports of life-threatening conditions reported from Florida and elsewhere represents an increase of risk caused by the COVID-19 vaccines is incorrect, misleading and could be harmful to the American public.” They are assuming unproven benefit at the start. The Bradford Hill criteria have been applied to VAERS and causality has been met. Autopsy studies have conclusively demonstrated causality for fatal syndromes. Doctors use the VAERS system when they believe COVID-19 vaccines caused the death, NOT when the death is unrelated to the vaccine in practice.
“The FDA-approved and FDA-authorized COVID-19 vaccines have met FDA’s rigorous scientific and regulatory standards for safety and effectiveness and these vaccines continue to be recommended for use by CDC for all people six months of age and older.” The FDA has relied on the false surrogate of antibody elevations after injection eight times. This is neither rigorous nor valid. Large randomized, double blind placebo controlled trials with hospitalization/death as the primary endpoint are required to prove efficacy in all age groups.
“Despite increased reports of these events, when the concern was examined in detail by cardiovascular experts, the risk of stroke and heart attack was actually lower in people who had been vaccinated, not higher.” They cite a nonrandomized study with inadequate control for the known determinants of cardiovascular disease. Both selection bias and confounding eliminate any valid claims of benefit. There is no mechanism by which COVID-19 vaccination would reduce cardiovascular events. There are >200 published manuscripts on COVID-19 vaccines mechanistically causing cardiovascular events including myocarditis, accelerated atherosclerotic cardiovascular disease, aortic dissection, hypertensive crisis, etc.
“FDA and CDC physicians continuously screen and analyze VAERS data for possible safety concerns related to the COVID-19 vaccines. For signals identified in VAERS, physicians from FDA and CDC screen individual reports, inclusive of comprehensive medical record review. Most reports do not represent adverse events caused by the vaccine and instead represent a pre-existing condition that preceded vaccination or an underlying medical condition that precipitated the event.” The agencies have not produced a report giving their analysis of what caused death after vaccination. Since many deaths occur on the day of the shot or in the next few days that follow, the public deserves to see regulatory evidence for cause of death.
“In addition to VAERS, FDA and CDC utilize complementary active surveillance systems to monitor the safety of COVID-19 vaccines.” CDC V-safe is one of the active systems mentioned. The CDC refused to release to the public until ordered by the courts, demonstrated an unacceptable 7-8% rate of hospitalization, emergency care, or urgent office visit caused by vaccine side effects. So agency use of systems demonstrate lack of safety and are not reassuring to the public.
“Based on available information for the COVID-19 vaccines that are authorized or approved in the United States, the known and potential benefits of these vaccines clearly outweigh their known and potential risks. Additionally, not only is there no evidence of increased risk of death following mRNA vaccines, but available data have shown quite the opposite: that being up to date on vaccinations saves lives compared to individuals who did not get vaccinated.” There are no randomized placebo controlled trials demonstrating hospitalization/death are reduced as primary endpoints. Thus the agencies cannot make an efficacy claim from a regulatory perspective. Nonrandomized studies have the following threats to validity: 1) selection bias—healthier more health conscious people take vaccines, 2) vaccinated are more likely to seek early treatment which reduces hospitalization/death, 3) no control over prior COVID-19 infection which greatly influences risk of hospitalization/death, 4) no adjudication of COVID-19 endpoints.
“Another study using mathematical modeling estimated that the vaccines saved an estimated 14 million lives from COVID-19 in 185 countries and territories between December 8, 2020, and December 8, 2021.” Modeling studies start with the unproven assertion that vaccination reduces death which has not been demonstrated in proper randomized trials, hence extrapolations to large populations are invalid.
“The most recent estimate is that those who are up to date on their vaccination status have a 9.8 fold lower risk of dying from COVID-19 than those who are unvaccinated and 2.4 fold lower risk of dying from Covid-19 than those who were vaccinated but had not received the updated, bivalent vaccine. Roughly 90% of deaths from COVID-19, as carefully classified by the CDC, in recent months have occurred among those who were not up to date on their vaccines.” This estimate did not account for the two known determinants of COVID-19 mortality: early treatment and natural immunity.
“Over the course of the pandemic, FDA and CDC have held numerous public meetings to discuss the safety and effectiveness of the COVID-19 vaccines where detailed safety data are shared with outside experts and public comment is encouraged. Further, FDA publishes the full regulatory action package containing hundreds of pages summarizing clinical studies and review for each COVID-19 approval on FDA’s website (see “COVID-19 Vaccines Authorized for Emergency Use or FDA Approved”) and CDC publishes an extensive amount of information on their clinical use in Interim Clinical Considerations. Complete information about both benefits and risks helps health care providers better care for their patients.” The FDA/CDC have never reviewed or commented on the Pfizer 90-day post-marketing data which reported 1223 deaths shortly after the shot. The FDA attempted to block these data to the public for 55 years. The agencies have never conducted a symposium to review the >1000 peer-reviewed published papers on serious adverse events and death after COVID-19 vaccination.
“Unfortunately, the misinformation about COVID-19 vaccine safety has caused some Americans to avoid getting the vaccines they need to be up to date.” The Rasmussen Report indicates 28% of Americans know someone who has died after the vaccine. Nothing in that report suggested “misinformation” was leading to hesitancy, moreover it was word of mouth on the horrifying outcomes Americans are witnessing among their family and friends that is leading to refusal rates of boosters.
There are easily another ten invalid assertions made by the agency that could be handled by experienced clinical investigators. Take a look at the letter yourself. Keep in mind the FDA/CDC deceived America by asserting that SARS-CoV-2 did not come out of the Wuhan Laboratory and just a few days ago the US House of Representatives voted to declassify our documents from the laboratory after multiple agencies and witnesses capitulated on the lab origin. This casts doubts on truthfulness of any agency public health assertions during the crisis.
The important message to Americans is that our agencies have no intention of carefully considering vaccine safety or changing course on their relentless pursuit of frequent, mass, indiscriminate COVID-19 vaccination down to 6-month old babies. It will be up to you to protect yourself and your family.
This is literally ‘hot off the ‘presses’: Austrian alternative media outlet Der Status published leaked documents from the Austrian Chamber of Physicians (Ärztekammer ) that show, beyond reasonable doubt, the grand conspiracy between government, the Chamber, and its protagonists.
Without much further ado, here’s my translation; as always, emphases and bottom lines mine. The below text has been lightly edited for clarity.
Scandal! Medical Association Ordered Experts & Doctors to Recommend Vaccination
The Austrian Medical Association, under the ousted red [i.e., Social-Democratic] president Szekeres and its current president Steinhart, worked closely with the Health Ministers for years. And in doing so, it betrayed the interests of doctors. [to say nothing about patients]
Spring 2020: Collaboration with the Politicians Commences
In April 2020, Szekeres, Steinhart, and Minister Anschober [Greens, since retired] signed a ‘Memorandum of Understanding Concerning COVID-19 Vaccinations’. That is, at a time—more than half a year—before the conditional approval of these injectable products, this Memorandum dealt with, among other things, advertising campaigns by doctors for the vaccinations, the vaccination of health-care workers and their family members, vaccinations in homes and schools, and reimbursement agreements.
Yet, secretly, an additional deal was also negotiated: it was literally agreed that ‘clear blanket vaccination recommendations will be made via the National Immunisation Consortium (Nationales Impfgremium, or NlG) on the suitability of the various vaccines and their applicability, esp. for various high-risk groups’.
Explosive: the Minister of Health and the Austrian Medical Association leadership signed a contract in which they go over the head of the National Immunisation Consortium—and they did so long before the injections were even available—to determine what the National Immunisation Consortium will recommend.
[this means, in other words, that the NIG never had anything to say about the data or the underlying clinical trials; this much we already knew, but now we have the receipts: these people have failed the public, betrayed the trust of patients, and soiled themselves]
It was never about Facts or Truth
Until now, the public was not aware of any document that so clearly showed that various ‘expert panels’ and ‘commissions’ obviously only served to obligingly recommend what politicians and the medical association leadership wanted. It was never about expertise, about advice, about objective science, about health.
Long before the beginning of the mass vaccination campaign, when vaccines did not even exist (!), it was only about one thing: vaccinate, vaccinate, vaccinate! The various ‘expert committees’ and doctors served only as Komparsen [extras, in German, one may also use the term Statisten, which literally implies undue influence of the state]. And it is obvious that the medical association leadership was ‘bought’ off with the reimbursement fee agreement [I’ve omitted the screen shots of some original documents, which can be checked out, if you read German, in the original article; it suffices to say that the fees are extraordinarily high, esp. in light of the incidence of injection: 25 Euros for the first jab and 20 Euros for every successive jab; this piece of evidence is reproduced below in the same position as in the original article]. April 2020 thus was the decisive moment in the history of the Medical Association in which its leadership handed the soul of the medical profession to politicians for the equivalent of thirty pieces of silver.
The Persecution of Doctors is Decided Upon
That was not all: in an ‘Amendments to the Memorandum of Understanding on COVID-19 Vaccinations between the Austrian Chamber of Physicians and the Ministry of Health, concluded in April 2020’, dated 2 Sept. 2021, the medical association leadership ‘promised action with respect to the services rendered by the medical profession’. These, too, signed off by both parties:
The Chamber of Physicians will conduct a media campaign as well as a campaign among the medical profession to increase the willingness of the population to be vaccinated. This includes raising the vaccination issue at other medical appointments (e.g., regular health check-ups) and the promise to take stronger action against doctors who spread misinformation.
As is well known, what constituted ‘misinformation’ was left to the arbitrary whims of the leadership of the Chamber of Physicians. This disgraceful agreement formed the basis for the persecution of critical doctors, which continues to this day. The medical disciplinary law was, in fact, misused for intimidation and propaganda purposes. In doing so, the leadership of the Chamber of Physicians had turned against its paying members [membership is mandatory in Austria as the Chamber also certifies physicians, much like these boards and associations in the U.S.], which cemented into place the persecution of doctors in the style of the Inquisition.
Disciplinary Proceedings by the Medical Association Were (Are) Illegal
The behaviour of the leadership of the Chamber of Physicians’ leadership in recent years is now coming back to haunt them. For months, the medical association has been attacked, ridiculed, and had its very existence openly questioned by politicians. Having done their duty for politicians in the last three years without a peep, the Chamber is apparently no longer needed and may well be let go of. The Chamber of Physicians is sinking more and more into political insignificance. According to insiders, it is now even regarded as a political opponent, a situation that can also be seen in legacy media. After having served as a ‘doormat’ for politicians of all stripes for years, the Chamber of Physicians is now also being treated as such. Various scandals internal to the medical association reinforce this tendency. [talk about Karma, eh? Those who don’t have self-respect will have a hard time getting others’ respect… ]
In the meantime, the Regional Administrative Courts of Vienna, Lower Austria, and Vorarlberg have petitioned the Constitutional Court to repeal parts or the entire Disciplinary Law in the Physicians’ Act [Ärztegesetz, these parts of the Act permit the Chamber of Physicians to enforce standards] on grounds of their suspected unconstitutionality; it is possible that the Constitutional Court will rule even the entire Physicians’ Act unconstitutional. The Chamber of Physicians is a self-governing body. All its committees are to be selected from among its members, i.e., from medical professionals. However, the Disciplinary Commission consists of two medical assessors and a ‘judicially competent chairman’ who is appointed by the Minister of Health in agreement with the Minister of Justice, i.e., someone who must not be a trained physician and who does not come out of the Chamber of Physicians. Thus, the composition of the Disciplinary Commission is a violation of the Federal Constitution. This is the unanimous legal opinion of three state administrative courts [Verwaltungsgerichtshof] and countless jurists.
[I’ll have more to say about this particularity below, for time being: this is potentially huge—and it would be akin to completely re-writing the rules of medicine]
The Chamber of Physicians has unintentionally awakened sleeping dogs with its wave of ill-advised disciplinary hearings against critical doctors. The consequence may be that it now has to be completely re-imagined. But this could also be an opportunity for the medical profession after all the repression of doctors in recent years. For in its current form, the Chamber of Physicians is a politically superfluous enemy and, for its members, the doctors, a very expensive mandatory association whose dues are used to finance the functionaries’ luxury salaries.
Bottom Lines
From time immemorial, we’ve all known that a man’s—or woman’s—price is about, in purely monetary terms, 30 pieces of silver, to say nothing about the amorality and, yes, cowardice of most physicians everywhere.
The notion of buying off support has been well-established in the U.S. (see, e.g., here).
Here, we’re talking individual doctors who are paid handsomely for jabbing people.
Yet, this isn’t even the worst part of this.
The Three Axioms of Governance-by-Bureaucracy
You’ve gotta love them German-speakers for being so stupid to actually put these things into writing.
We now have definitive proof that the subsequent shenanigans—first and foremost the obnoxious Covid Passports — were based on the unholy trinity of questionable medical ethics (ahem), government coercion, and arbitrary definitions.
Remember that ‘fully vaccinated’ used to be two injections? Now it’s at least three, with the fourth jab ‘optional’ (haha, see above), and the Covid Passports come with expiration dates varying from 3-6 months, irrespective whether you’re ‘vaccinated’ or ‘recovered’.
Thus, we may formulate whatthe first axiom of governance-by-bureaucracy is: everything leaks.
In other words: arbitrary categories by government fiat, arrived at with the collaboration of the overwhelming majority of the medical profession.
If history is any guide, the Covid Passports are the functional equivalent of the Aryan Certificate deployed by Nazi Germany: both documents were clearly politically motivated and based on sham ‘The Science™’.
Yet, Covid is revelatory: we’ve seen the abject lack of integrity, morality, and compassion on part of the political caste, its willing executioners in legacy media, and its perpetrators among medical professionals.
Don’t ask what’s wrong with individuals. It’s the bloody ‘system’ that stands exposed.
Thus, we may formulate the second axiom of governance-by-bureaucracy: everyone has his or her price.
We’ve known this for quite some time; sure, I could cite the Nazi and Stalinist atrocities here, but I’d like to point you also to the Asch Conformity, the Milgram, and the Stanford Prison Experiments. Or the book The Wave.
And yet, despite all of this, there’s also a bright spot in all of this: contrary to the claims of postmodernist woke-fied agents-provocateurs, not everything in human society and relations is ‘socially constructed’ or about ‘power’.
A sizeable share of people everywhere has resisted the pressure to ‘get vaccinated’.
A group of doctors have resisted the pressures and temptations—remember the 30 pieces of silver—of collaboration and compliance with government tyranny.
If ‘booster’ uptake is any guide, more and more people are realising that they’ve been had.
Thus the third axiom: incentives and coercion work, until they don’t.
Our highly complex societies are, of course, more than the sum of their moving parts. Yet, given the highly integrated structures, it would be far-fetched to believe that anyone is able to control everything.
True, a lot can be dominated, but in the end, the ‘normative power of the factual’ (Georg Jellinek), in combination with individual experiences, is a powerful antidote to tyranny.
Still, this ain’t over yet, far from it.
If history is any guide, all that humans have ever been able to do is punish the perpetrators in the (vain) hope of establishing deterrence.
It has happened before, it is happening again, and it will happen again.
The next step is to see this through, re-establish the rule of law, and hold these people to account.
California legislators continue their reign of vaccine mandate terror with the proposed Assembly Bill 659, which would require children to be vaccinated for HPV before entering 8th grade. Attorney, Michael Baum, Esq., discusses his law firm’s fight to block this bill, which would stop countless crippling injuries, especially in the absence of proof of efficacy.
In the aftermath of the release of the Lockdown Files, the public is slowly coming to terms with some fairly shocking facts: that the Government was willing to lie and mislead, and to scaremonger and manipulate the media, in order to achieve its Covid policy objectives (or even just to garner a few headlines). The news is still sinking in, but a day of reckoning for those involved looks likely.
For those of us bearing the scars of long engagement in the climate and energy wars, however, none of this was a surprise. It has long been clear that the inhabitants of the Westminster village were happy to hype up fears of climate purgatory and to fib about the road to redemption – renewables – and the cost of taking it. Once the public understand the depth and extent of the deception, and the damage done to the economy and the prospects for our children, the trickery over Covid is going to look decidedly peripheral.
The latest report from the Climate Change Committee (CCC) is a case in point. On the surface it’s a roadmap to a decarbonised electricity grid, but in reality it’s merely a sales document, full of tricks, evasions and outright falsehoods that would make even the most cynical used car salesman blush.
For example, in a number of places, it says that decarbonisation of the grid will be ‘cost-effective’, but you will find next to no information on what it will cost. The game that is being played becomes a bit clearer when you read the reference to ‘carbon prices’. In normal usage, the carbon price is the estimate of the damage done by a ton of carbon dioxide, but in the CCC’s parlance it is an estimate of what it will cost to decarbonise. So, while it gives you the impression it has done a cost-benefit analysis and is going to be saving you money, in reality it is only saying that the bill to be paid will be the same as previously advised. It’s a trick.
Another trick is to assume that wind power costs will be only a quarter of what they actually are. For years, the industry has been pushing claims that they have brought about a cost-reduction revolution. The problem is that windfarms’ own financial accounts show that it isn’t true. And with new windfarms now saying they will not come on stream without further subsidies, the deception has been exposed.
I’m picking on the CCC here, simply because it is in the news today. But it’s not just the CCC. None of the bodies whom the public expect to tell the truth about the Net Zero project will do so: the Royal Academy of Engineering is silent. The Royal Society likewise. National Grid pretends the task is a cinch. The National Infrastructure Commission just repeats the Government line verbatim. Parliament asks how soon the job can be done, not whether it can be done or how much it will cost. Everywhere the tricks go unchallenged and the lies are swept under the carpet.
Such deceptions mean that we are storing up catastrophic harms for our economy, and for our children and grandchildren. Energy that was said to be as cheap as gas is actually going to cost three or four times as much. The costs of ensuring supply when the wind doesn’t blow are an order of magnitude larger.
And whether it was delivered on the back of a lie or not, you are going to have to pay for it. A huge pipeline of wind projects is in place already, each eligible for an astonishing array of hidden subsidies – the list is too long to give here. Once built, they will suck wealth from our economy and hope from our society. They will be hard, if not impossible, to close down – they have been made exempt from windfall taxes and the Government cannot simply switch them off without destroying investor confidence in the economy as a whole. If we do not reverse course soon, our children will never know the wealth we have enjoyed until now, just poverty and rationing and hardship. And all because everyone is too scared to challenge the lies. Just like Covid.
Public health experts are warning that the ‘air testing’ being carried out in East Palestine by a for-profit company hired by Norfolk Southern is “almost like smoke and mirrors.”
The ‘air testing’ recently conducted in East Palestine residents’ homes was deficient in a number of key ways and was actually carried out by a company contracted by the rail company Norfolk Southern, a new report has revealed.
East Palestine, Ohio was smothered in toxic fumes last month when the authorities intentionally burned off huge quantities of vinyl chloride following a train derailment in the village.
Residents fled the area in the immediate aftermath. However, after an evacuation order was lifted, many have returned, with some reportedly citing ‘air testing’ results which apparently determined that they could return home without danger.
But on Saturday, an explosive new report seemed to confirm what many have come to suspect: “the air testing results did not prove their homes were truly safe.”
According to a major British outlet, “the air tests were inadequate in two ways: they were not designed to detect the full range of dangerous chemicals the derailment may have unleashed, and they did not sample the air long enough to accurately capture the levels of chemicals they were testing for.”
As University of Kentucky environmental health professor Erin Haynes reportedly put it, “it’s almost like if you want to find nothing, you run in and run out.”
Making matters even worse, “CTEH, the contractor that provided them, was hired by Norfolk Southern, the operator of the freight train that derailed,” the report detailed.
As another outlet previously explained, “the Center for Toxicology and Environmental Health (CTEH) has a name that might sound like a state or federal agency, but in reality it is a private, for-profit corporation that has been present after hundreds of ecological disasters—from 9/11 to Hurricane Katrina to the Deepwater Horizon oil spill to COVID-19.”
While the relevant section has since been deleted, the company previously explained on its website how the data it’s collecting now could be weaponized against the victims of the Norfolk Southern train derailment disaster in East Palestine:
“A carrier of chemicals may be subjected to legal claims as a result of a real or imagined release,” CTEH noted, adding, “should this happen, appropriate meteorological and chemical data, recorded and saved… may be presented as powerful evidence to assist in the litigation or potentially preclude litigation.”
But despite its alarming track record and apparent desire to go after those affected by the crisis, the company remains a major force in the campaign to assuage locals’ health fears.
“It was CTEH, not the Environmental Protection Agency (EPA), that designed the testing protocol for the indoor air tests,” explains the British report, adding, “and it is CTEH, not the government, that runs the hotline residents are directed to call with concerns about odors, fumes or health problems.”
In a recently-published video, the controversial company insists that their ‘testing’ shows there’s no danger to East Palestine residents.
“All of our air monitoring and sampling data collectively do not indicate any short- or long-term risks,” a CTEH toxicologist claimed.
But CTEH’s failure to register so-called volatile organic compounds (VOCs) in its tests doesn’t necessarily mean that people’s homes are actually safe, a number of experts noted. As Haynes reportedly explained, “VOCs are not the only chemicals that could have been in the air.”
And even a week after the derailment, she said it’s likely the compounds would have dissipated already.
“To keep the focus on the air is almost smoke and mirrors,” Haynes added. “Like, ‘Hey, the air is fine!’ Of course it’s going to be fine. Now you should be looking for where those chemicals went. They did not disappear. They are still in the environment.”
You may have heard that Marburg virus is rearing its ugly head in west Africa. The subtext is Be Very Afraid.
Just in time, the NIAID (Fauci’s old fiefdom) has a vaccine ready to be tested in unfortunate Africans, after being tested on 40 unfortunate Americans. And once they convince governments or other buyers to obtain it, who gets royalties? Why NIAID of course. And its employees can collect up to $150,000/year if their name is on the patent. Sweet, since it was developed and patented on the taxpayers’ dime.
This first-in-human, Phase 1 study tested an experimental MARV vaccine candidate, known as cAd3-Marburg, which was developed at NIAID’s Vaccine Research Center (VRC). This vaccine uses a modified chimpanzee adenovirus called cAd3, which can no longer replicate or infect cells, and displays a glycoprotein found on the surface of MARV to induce immune responses against the virus. The cAd3 vaccine platform demonstrated a good safety profile in prior clinical trials when used in investigational Ebola virus and Sudan virus vaccines developed by the VRC [NIAID’s Vaccine Research Center].
So they claim the Ebola vaccine, also using the adenovirus platform, has a good safety profile—well, the death rate in the 2018-19 east African epidemic was 60%, higher than usual Ebola epidemics. The vaccine was widely used there—so did the disease kill people or the vaccine? Why were there 300 attacks on health workers, many of whom were vaccinators? I don’t think that imputing safety to the Ebola vaccine is acceptable, nor that the Ebola vaccine can be used to impute safety of the Marburg vaccine. Why did the NIAID only test the vaccine in 20 Americans if there were no serious adverse events, and it was so safe?
Plans are in place to conduct further trials of the cAd3-Marburg vaccine in Ghana, Kenya, Uganda, and the United States. If additional data supports the promising results seen in the Phase 1 trial, the cAd3-Marburg virus vaccine could someday be used in emergency responses to MARV outbreaks.
Yes, the adenovirus vector platform, which was known even before the pandemic to cause blood clots. (I have blogged on this.) And clearly proven to cause venous sinus clots around the brain with the J and J and Astra-Zeneca adenovirus vector COVID vaccines.
Marburg: CDC lists a total of 475 lab-confirmed cases during the entire 56 years since Marburg was first identified. How was it identified? It came to Europe with monkeys from Africa, affecting lab workers, of whom 7 of 31 (23%) died.
Marburg is clinically like Ebola, which has affected thousands, but still—in the US Ebola only spread from affected patients to 2 nurses and never spread further. There have been no US Marburg cases. Neither of these infections is very contagious. Using reasonable precautions you won’t get them.
My point is that the risk to us from a natural virus or bacterium is miniscule. That may not be true of a lab-developed microorganism.
It is the lab-designed bugs that are the problem. We need to stop them. Close the labs, the BSL4s, reduce the BSL3’s and get rid of basic research on “selected agents,” destroy the samples, end this form of “science” that has proven its ability to kill millions and cause worldwide economic destruction. End the field of virology and evolutionary viral genetics—which seem to be peopled by a large group of ‘scientists’ who were in cahoots to keep the lab origin covered up…or at a minimum were afraid to tell the public the truth. Keep a few medical virologists around who did not get their hands dirty. Who needs most of them? They have proven their societal value—which is NEGATIVE—over and over these last three years.
I will shed no tears if they are forced to go and do some manual labor in future. Will you?
Put tight price controls on vaccines, allow about 5% profit, and the wild west in vaccinology will disappear. End pandemic preparedness, from which the money for all the new BSL4s and the new coronaviruses in the US came.
We need to get clear on this. The naturally occurring bugs don’t cause deadly pandemics. They do kill off some weak and frail people in the developed world, and occasional a virus or bacterium will kill a young person. Those deaths are unpredictable and the bugs, often unidentified, don’t really spread beyond an occasional case or two. We have no viable path for preventing them. The so-called “spillover” infections can hardly be found.
It is the Global Biosecurity Agenda that must be stopped.
Doctor and nurse deaths from COVID-19 vaccines were always going to be the focus of cover-ups. The reason is practical: the state needs doctors and nurses to enthusiastically push COVID-19 vaccines on their patients, and it needs these same doctors and nurses to stay silent about COVID-19 vaccine injuries and deaths.
Doctors and nurses mustn’t know that their colleagues are dying suddenly from the same COVID-19 mRNA vaccines that they are pushing daily on their own patients.
31 year old NZ nurse died 4 days after booster shot
Divya Simon, 31, a rest home nurse, had her third COVID-19 booster vaccination four days before suffering a massive heart attack, according to a decision from coroner Luella Dunn released today. (click here)
“She had the booster on January 25 last year, and took the next day off work because she felt unwell. She complained of pain in the left side of her neck and shoulder.
Simon, who had two children aged 4 and 2, worked a night shift on January 28 returning home early the next morning and went to sleep at 10am. After she woke mid-afternoon she went to have a shower and told her husband she felt dizzy and had chest pains. That evening she had a cardiac arrest.
Ambulance arrived and Simon was given adrenalin, shocked and taken to Waikato Hospital. There she was intubated and taken to ICU but was not responsive and continued to deteriorate, dying the next day at 11am.
Dunn said an angiogram was unable to determine the cause of the cardiac arrest and there were no medical records to indicate why Simon would suffer a heart attack.
The pathologist who conducted her autopsy told the coroner Simon’s death was most likely related to an underlying weakness in her coronary arteries.
The pathologist found no evidence to suggest Simon’s vaccination contributed in any way to her death and the Centre for Adverse Reaction Monitoring came to the same conclusion.”
Case Closed!
That’s it. Case closed. A healthy 31 year old nurse had a massive heart attack 4 days after her COVID-19 booster shot and it was definitely not the booster shot, although the pathologist had no idea why she died.
But the pathologist is lying. And I can prove it.
New Zealand does not perform autopsies with immunohistochemical staining of tissue samples for the COVID-19 vaccine spike protein.
So when the pathologist said he “didn’t find evidence” of COVID-19 vaccine damage, that was a lie. He “didn’t find evidence” because he didn’t look for it – he did not conduct the proper staining of the pathology samples, because no one in New Zealand does.
“There is no current test (in New Zealand) that will show the Covid-19 vaccine in the heart tissue” as reported by One News New Zealand (click here)
26 year old NZ man died of myocarditis due to Pfizer COVID-19 Vaccination
Let’s look at a different case where the pathologist linked a sudden death to the Pfizer COVID-19 mRNA vaccine – the case of 26 year old NZ man Rory Nairn (click here)
Rory Nairn died of myocarditis after 1st dose of Pfizer COVID-19 vaccine.
Coroner Sue Johnson opened an inquiry into his death. After hearing evidence from pathologist Dr Noelyn Hung, Johnson said she is satisfied that the COVID-19 vaccine caused the myocarditis from which Nairn died.
Hung carried out an intensive pathological examination of the heart. She stated that the cause of the myocarditis came down to a diagnosis by exclusion.
There is no current test that will show the Covid-19 vaccine in the heart tissue, but Hung was able to exclude other causes of myocarditis. Hung also excluded all other known potential causes including certain medicines.
There was no sign of any infection or any other reason for Nairn’s death except in the myocardium (the middle muscular layer of the heart). Johnson accepted Hung’s medical opinion that the direct cause of Nairn’s death was acute myocarditis – consistent with vaccine-related myocarditis.
What this means
If there is no test available to check for COVID-19 vaccine injury to body tissues, you cannot exclude the vaccine as the cause of death. In the case of the 31 year old nurse Divya Simon, the pathologist cannot conclude “the COVID-19 vaccine didn’t do this” or “there is no evidence the COVID-19 vaccine did this”. It is not possible to come to this conclusion, because the pathologist had no way of proving this.
In the case of 26 year old Rory Nairn, COVID-19 vaccine myocarditis was declared the cause of death because every other possibility was excluded. It was the diagnosis of exclusion.
Notice the difference?
The 31 year old nurse death was a cover-up. The pathologist lied. New Zealand’s Centre for Adverse Reaction Monitoring lied. They covered-up her death. Almost certainly because she was a nurse.
My Take…
It should not surprise anyone by this point, that deaths of doctors and nurses will be treated very differently and will be covered up at all costs.
When 3 Canadian doctors died within days of each other in the same Trillium Health Hospital in Mississauga, Ontario, days after the rollout of the 4th COVID-19 vaccine (2nd booster shot), mainstream media called it a coincidence (click here) (click here)
That’s why my reporting on 132 Canadian doctor sudden deaths since the rollout of the COVID-19 vaccines has been so “controversial”.
The fiercest attacks I have faced from mainstream media so far, were about me exposing the sudden deaths of fully COVID-19 vaccinated Canadian doctors.
So whenever you see a case like this where a coroner or pathologist declares that “COVID-19 vaccine didn’t cause this death”, you will know they are lying, and you will be able to explain exactly why they are lying.
They can allow the occasional citizen’s death to be linked to the COVID-19 vaccine. But they cannot and will not allow a doctor or nurse’s death to be linked to the vaccine.
The Telegraph’s publishing of former UK Health Czar Matt Hancock’s private Whatsapp messages has been dubbed ‘The Lockdown Files.’ The messages detail multiple interactions demonstrating the U.K. Government’s willingness to abandon science and a reasoned approach to Pandemic measures, for coercion and control of the British people.
Former CDC Director, Dr. Robert Redfield, testified before The House Selection Committee on the Coronavirus Pandemic this week, letting loose on Anthony Fauci, Deborah Birx, Francis Collins, gain-of-function research and the lab origin debate detailing what he witnessed in early 2020. His testimonials are nothing short of historical.
Now that they’ve stopped telling the public to constantly cover their mouths, Japan’s government and media have moved on to telling the public to put bugs into them. And who better to advocate for people to put insects down their throats than the man who advocated most actively for people to put mRNA injections into their veins, former Vaccine Minister and current Digital Minister Taro Kono?
Taro Kono tries crickets at a venture firm exhibition, Says they are “delicious”.
Here’s a better look at the “delicious” crickets Mr Kono pulled his mask down to taste.
But since about 90% of Japanese are resistant to the idea of eating bugs, Japan’s politicians and propaganda apparatus will have to work harder at pushing crickets than they did pushing Covid jabs. Reworking some of its greatest hits from the Covid era, the media has declared “neophobia” to be the new “vaccine-hesitancy”.
Is revulsion to edible crickets due to neophobia (fear of new things)?
So are the neophobes selfishly preventing the creation of a “sustainable” society with their anti-cricket stance? Or do they have a point in sticking to foods humans have actually evolved to consume? Let’s ask the science.
In an 2018 article entitled “Novel foods: a risk profile for the house cricket”, Jannson et al. conducted a literature review to present a risk profile of house crickets as food. They found four potential concerns.
(1) high total aerobic bacterial counts; (2) survival of spore-forming bacteria following thermal processing; (3) allergenicity of insects and insect-derived products; and (4) the bioaccumulation of heavy metals (e.g. cadmium).
The aim of this study was to identify and evaluate the developmental forms of parasites colonizing edible insects in household farms and pet stores in Central Europe and to determine the potential risk of parasitic infections for humans and animals. The experimental material comprised samples of live insects (imagines) from 300 household farms and pet stores, including 75 mealworm farms, 75 house cricket farms, 75 Madagascar hissing cockroach farms and 75 migrating locust farms. Parasites were detected in 244 (81.33%) out of 300 (100%) examined insect farms. In 206 (68.67%) of the cases, the identified parasites were pathogenic for insects only; in 106 (35.33%) cases, parasites were potentially parasitic for animals; and in 91 (30.33%) cases, parasites were potentially pathogenic for humans. Edible insects are an underestimated reservoir of human and animal parasites.
Among the various parasites potentially pathogenic for humansfound in cricket samples were the following.
Isospora spp. [found in 2.67% of samples from cricket farms] are cosmopolitan protozoa of the subclass Coccidia which cause an intestinal disease known as isosporiasis. These parasites pose a threat for both humans (in particular immunosuppressed individuals) and animals. The host becomes infected by ingesting oocytes, and the infection presents mainly with gastrointestinal symptoms (watery diarrhea).
Physaloptera spp. [found in 1.33% of samples from cricket farms] form cysts in the host’s hemocoel approximately 27 days after ingestion.
Although both above-mentioned papers point to various potential issues, they admit there isn’t enough evidence yet to draw conclusions about the health effects of mass-production and mass-consumption of crickets. And I’d say we’re better off keeping it that way, no matter what names the globalist overlords call us.
On February 1st this year, the World Health Organisation released the first draft of its much heralded pandemic response treaty. The draft treaty, snappily titled the ‘Convention or Agreement on Pandemic Prevention, Preparedness and Response’, is proposed as a solution to what the WHO calls the “catastrophic failure of the international community in showing solidarity and equity” during the “coronavirus pandemic”.
A supposed lack of solidarity amongst national governments will not be the “catastrophic failure” uppermost of many readers’ minds when thinking back on Government health policy over the last three years. Despite this, the WHO’s draft treaty proposes preventing a recurrence of this alleged failure by substantially enhancing the powers of the WHO relative to those of national health authorities.
It does this despite initially affirming “the principle of sovereignty of States Parties in addressing public health matters” in its opening recital, and despite recognising the principle of state sovereignty as one of the guiding principles of the treaty in article 4. Yet notwithstanding these reassuring nods to the notion of state sovereignty, the WHO’s real attitude towards state autonomy can be gauged by a quick glance at the rest of the recitals and provisions in the agreement.
In setting out the WHO’s interpretation of the factual background to this draft agreement, many of the other recitals focus on the purported practical inability of individual sovereign states to respond adequately to the unique health challenges of the modern world. Hence other recitals note that “a pandemic situation is extraordinary in nature, requiring States Parties to prioritise effective and enhanced cooperation”; that “the international spread of disease is a global threat with serious consequences… that calls for the widest possible international cooperation”; and that “the threat of pandemics is a reality and that pandemics have catastrophic health, social, economic and political consequences”. These recitals strongly imply that state sovereignty can be of limited importance in the face of such extraordinarily grave threats.
Similarly, while recognition of state sovereignty is given as one of the guiding principles of the agreement, it is somewhat overshadowed by the raft of other guiding principles, which include abstract things like “equity”, “solidarity” and the “right to health”. Indeed, article 4 goes on to ominously assert that “previous pandemics have demonstrated that no one is safe until everyone is safe”, strongly suggesting that adherence to the principle of national sovereignty during a pandemic is not just an outdated approach to take, but a positively selfish one.
The draft agreement therefore goes on to assign considerable power to the WHO to influence and shape the responses of national health authorities to any future pandemic. The breadth of ambition of the agreement is made clear in article 5, which applies the agreement in a far-reaching way to “pandemic prevention, preparedness, response and health systems recovery at national, regional and international levels”.
Subsequent articles go on to prescribe the policies to be followed by States Parties to the agreement in each of these areas. As examples of what is intended, articles 6 and 7 set out steps to be followed to improve logistics and the workings of the global supply chain for quicker dispersal of what are euphemistically termed “pandemic-related products” (read pharmaceuticals), after which article 8 of the agreement addresses “regulatory strengthening”. Sadly, the regulatory strengthening envisaged in this agreement is not the strengthening of the accountability of national health regulators to the public, but rather the strengthening of those regulators’ accountability to the inter-governmental blob. Article 8 therefore requires signatory states to “strengthen the capacity and performance of national regulatory authorities and increase the harmonisation of regulatory requirements at the international and regional level”. In layman’s terms, more funding and powers for the regulators, yet concurrently less independent decision-making from them as well.
Subsequent articles further limit the discretion of national health authorities in responding to future WHO designated pandemics. Article 11 requires signatory states to “adopt policies and strategies… consistent with… the International Health Regulations” (themselves the target of amendment by the WHO), while article 15 stresses “the need to coordinate, collaborate and cooperate, in the spirit of international solidarity” with the various bodies active in the international healthcare space in the formulation of policies and guidelines. There are references to “establishing appropriate governance arrangements”, presumably well away from potentially meddlesome interference by elected representatives. These governance arrangements are to be complete with “mechanisms that ensure global, regional and national policy decisions are science and evidence-based”. Think blanket mask and vaccine mandates.
Signatory states will also have to take part in “multi-country or regional tabletop exercises every two years” to prepare them for the next pandemic, presumably to ensure that all health authorities remain fully briefed on the acceptable line to take in the event of any such new pandemic being declared, and to deter any of the signatory states from being tempted to go off-script as Sweden did in 2020.
Last but not least, a plethora of comfortable sinecures will be created for the international administrative class, by way of the creation of a governing body for the agreement under article 20, a consultative body for input into decision making by amorphous inter-governmental stakeholders under article 21, and a secretariat under article 24.
Conspicuously lacking in the agreement is any reference to democracy, elected legislatures, or the necessity of regulators and health authorities being accountable to national electorates. Instead, the treaty represents a brazen attempt to further move health policy away from regional or national governments and into the hands of a rarefied class of globalist administrators.
It should be stressed that the current text is only a draft, and that it may be subject to amendments following discussion between the WHO and member states. Further, even if the U.K. does sign this agreement, it will likely require ratification by Parliament under the Constitutional Reform and Governance Act 2010, and will also require implementation via domestic legislation before it will have any domestic legal effect in the U.K. Sustained pressure now on ministers and MPs might just influence any U.K. Government proposals to amend the treaty at draft stage, or alternatively such pressure might conceivably prevent the U.K. Government from signing an unacceptably worded agreement in the first place. Either way, now is the time for action to prevent the crystallisation at international level of the very policies and approaches many of us have railed against at national level for the last three years.
Adam Cross (a pseudonym) is a U.K. qualified barrister specialising in international trade law, with both public and private sector experience.
By Prof. Tony Hall | American Herald Tribune | July 17, 2016
The Kevin Barrett-Chomsky Dispute in Historical Perspective – Fourth part of the series titled “9/11 and the Zionist Question”
Back in 2006 all but a prescient few, such as Christopher Bollyn, perceived it as premature to try to identify and bring to justice the actual perpetrators of the 9/11 crimes. There was still some residue of confidence that responsible officials in government, law enforcement, media and the universities could and would respond in good faith to multiple revelations that great frauds had occurred in interpreting 9/11 for the public.
Accordingly, the main methodology of public intellectuals like Dr. Kevin Barrett or, for instance, Professors David Ray Griffin, Steven E. Jones, Peter Dale Scott, Graeme MacQueen, John McMurtry, Michael Keefer, Richard B. Lee, A.K. Dewdney, Nafeez Mossadeq Ahmed, and Michel Chossudovsky, was to marshal evidence demonstrating that the official narrative of 9/11 could not be true.
The marshaling of evidence was spurred on by observations coming from government insiders like Eckehardt Wertherbach, a former head of Germany’s intelligence service. In a meeting in Germany with Christopher Bollyn and Dr. Andreas von Bülow, Wertherbach pointed out that, “an attack of this magnitude and precision would have required years of planning. Such a sophisticated operation would require the fixed frame of a state intelligence organization, something not found in a loose group like the one led by the student Mohammed Atta in Hamburg.”
Andreas von Bülow was a German parliamentarian and Defense Ministry official. He confirmed this assessment in his book on the CIA and 9/11. In the text von Bülow remarked that the execution of the 9/11 plan “would have been unthinkable without backing from secret apparatuses of state and industry.” The author spoke of the “invented story of 19 Muslims working with Osama bin Laden in order the hide the truth” of the real perpetrators’ identity. … continue
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