The Most Revolutionary Act

Uncensored updates on world events, economics, the environment and medicine

The Most Revolutionary Act
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About stuartbramhall

Retired child and adolescent psychiatrist and American expatriate in New Zealand. In 2002, I made the difficult decision to close my 25-year Seattle practice after 15 years of covert FBI harassment. I describe the unrelenting phone harassment, illegal break-ins and six attempts on my life in my 2010 book The Most Revolutionary Act: Memoir of an American Refugee.

Scientific American Issues Severe Warning on 5G

Terence Newton
Waking Times

In a recently published article entitled, We Have No Reason to Believe 5G is Safe, Scientific American (SciAm) magazine issued a stern warning about the known and potential dangers of 5G technology.

Of particular significance is the fact that SciAm is the oldest continuously published monthly magazine in the United States, founded by inventor and publisher Rufus M. Porter in 1845, and running monthly since 1921. It is a highly influential publication, widely reputed for its rigorous scientific standards, and lauded by today’s fact-checkers as highly credible and staunchly pro-science.

In the article, University of California, Berkeley public health researcher Joel M. Moskowitz argues that 5G, along with previous w-fi and cellular technology, is much more harmful than the government and telecomm industry wants the public to believe.

His primary concerns center around a recent FCC announcement, made in a press release, that the FCC is close to reaffirming the radio frequency radiation (RFR) exposure limits that were previously adopted by the commission in the 1990’s… well before the introduction of 5G, 4G, 3G, 2G or even WiFi.

In short, the safety standards that the FCC wishes to maintain are severely outdated and fail to reflect the growing body of scientific evidence demonstrating harm.

Moskowitz notes that the ’90’s exposure limits only address the singular concern over the potential effects of the intensity of exposure to RFR. With the research we now have available the health concerns are much broader, including a sincere risk of cancer, among other things.

“The latest cellular technology, 5G, will employ millimeter waves for the first time in addition to microwaves that have been in use for older cellular technologies, 2G through 4G. Given limited reach, 5G will require cell antennas every 100 to 200 meters, exposing many people to millimeter wave radiation. 5G also employs new technologies (e.g., active antennas capable of beam-forming; phased arrays; massive multiple inputs and outputs, known as massive MIMO) which pose unique challenges for measuring exposures.

Millimeter waves are mostly absorbed within a few millimeters of human skin and in the surface layers of the cornea. Short-term exposure can have adverse physiological effects in the peripheral nervous system, the immune system and the cardiovascular system. The research suggests that long-term exposure may pose health risks to the skin (e.g., melanoma), the eyes (e.g., ocular melanoma) and the testes (e.g., sterility).

The FCC’s RFR exposure limits regulate the intensity of exposure, taking into account the frequency of the carrier waves, but ignore the signaling properties of the RFR. Along with the patterning and duration of exposures, certain characteristics of the signal (e.g., pulsing, polarization) increase the biologic and health impacts of the exposure. New exposure limits are needed which account for these differential effects. Moreover, these limits should be based on a biological effect, not a change in a laboratory rat’s behavior.” ~Joel M. Moskowitz, Scientific American

Moskowitz also cites the the International EMF Scientist Appeal, which elaborates on the now-known dangerous effects of RFR:

“Numerous recent scientific publications have shown that EMF affects living organisms at levels well below most international and national guidelines. Effects include increased cancer risk, cellular stress, increase in harmful free radicals, genetic damages, structural and functional changes of the reproductive system, learning and memory deficits, neurological disorders, and negative impacts on general well-being in humans. Damage goes well beyond the human race, as there is growing evidence of harmful effects to both plant and animal life.” [Source]

Moskowitz points out that,”the scientists who signed this appeal arguably constitute the majority of experts on the effects of nonionizing radiation. They have published more than 2,000 papers and letters on EMF in professional journals.” Inviting readers and policy makers to consider the weight of more than 500 peer-reviewed research studies finding, “harmful biologic or health effects from exposure to RFR at intensities too low to cause significant heating,” Moskowitz believes that more rigorous studies are necessary before the rollout goes forward.

In other words, the scientific jury is already out on the harmful effects of RFR, and the FCC is flat-out derelict in its duty to put public safety above telecomm industry interests.

Regarding the propaganda dimension of this debate, Moskowitz addresses the fact that industry spokepersons and related government officials frequently refer to contrarian viewpoints as ‘fear-mongering,’ pointing out that the current scientific research is legitimate, leaving the scientific community with a genuine responsibility to speak out about these concerns.

“The telecommunications industry and their experts have accused many scientists who have researched the effects of cell phone radiation of “fear mongering” over the advent of wireless technology’s 5G. Since much of our research is publicly-funded, we believe it is our ethical responsibility to inform the public about what the peer-reviewed scientific literature tells us about the health risks from wireless radiation.” ~Joel M. Moskowitz, Scientific American

Final Thoughts

Cracks are showing in the government and telecom industry’s blanket assertion that 5G is safe, and many prominent and influential scientists, dignitaries, and organizations are now speaking out against 5G – the global human experiment without consent.  For the editorial board of Scientific American to run a piece this condemning 5G is a very strong signal that even the most mainstream elements of the scientific community are genuinely concerned.

Via https://www.wakingtimes.com/scientific-american-the-oldest-us-monthly-magazine-issues-severe-warning-on-5g/

US Figure: From 10 million Jabbed, 770,000 Needed Medical Care

Cracks everywhere in narrative – but MSM continues to bury its head

THE wall of defiance and secrecy that protects the Covid jab narrative is crumbling so fast that one can see right through to the deceitful heart of this medical scandal.

To quote Leonard Cohen: “There’s a crack in everything – that’s how the light gets in” and thank God for that.

The latest beam of truth comes from American lawyer Aaron Siri, who revealed some damning statistics in an interview with Fox News.

Siri has been trying to force the Centers for Disease Control and Prevention (CDC) to release data on jab side-effects. After 463 days and two law suits, he finally has the figures.

And they are shocking.

Of 10million users on the CDC’s V-Safe system, 7.7 per cent had to seek medical care after vaccination.

He says: “That’s an incredible percentage, it seems to me.”

It is simple maths. No less than 770,000 people required medical treatment after the Covid jab from a sample of just 10m. On top of that, 25 per cent – or two and half million – took time off from work or school after an injection.

The population of America is 330m and most States have pursued an aggressive jab policy, so just how much damage has really been caused? Their VAERS system is currently showing more than 30,000 reports of jab-related deaths; it is highly plausible that this represents an underestimate by a factor of 10, at least.

Of course, none of the above has been reported in UK mainstream media which, GB News excepted, remains wilfully blind to the mountain of evidence.

News Uncut has been consistent with concerns over one-sided news reporting, together with the suppression of opposing opinions in MSM and social media, the labels of ‘misinformation’ and the cancelling of eminent voices who dared to speak out.

The Trusted News Initiative, “an industry collaboration of major news and global tech organisations working together to stop the spread of disinformation,” is at the heart of this censorship and, shamefully, the BBC is a prominent participant along with Facebook, Google, Twitter and YouTube, to name just some. They have pronounced the facts and denied any counter argument, any fair debate.

In the recently released film Safe and Effective: A Second Opinion, the BBC was asked what happened to impartial reporting, balance and free speech. They refused to comment.

Now the Under-Secretary-General for Global Communications at the United Nations, Melissa Fleming (below), has admitted that the UN partnered with several big tech companies to control Covid and climate narratives while claiming “We own the science”.

Speaking at the World Economic Forum’s (WEF) Sustainable Development Impact meetings, Fleming told a panel on Tackling Disinformation that the UN had partnered with Google so that ‘authoritative’ narratives would appear at the top of search results.

Meanwhile, a judge in America has ordered the White House to release emails between various federal Agencies and Big Tech companies, with the paintiffs alleging collaboration over the suppression of free speech and information on Covid and the associated jabs.

[…]

Via https://uncut.substack.com/p/us-figures-from-10million-jabbed

Hidden History: Link Between Opus Dei, Western Intelligence and Child Trafficking

Opus Dei: Faith, Power and Manipulation

DW (2021)

Film Review

The video below is a sanitized vanilla-light documentary on Opus Dei. The latter was propelled to wide public attention by Dan Brown’s 2003 book The Da Vinci Code and the 2006 movie based on the book. Contrast it with the classic 1983 Mother Jones article “Thy Will Be Done,” and the 2019 ISGCP article linked in the last paragraph.

The documentary poses more questions than it answers. According to DW, Opus Deis was  founded by Catholic priest Josemaría Escrivá de Balaguer in Navarre Spain in 1928. Escriva and his followers strongly supported Spanish dictator Francisco Franco, who rewarded Opus Dei with powerful positions in his fascist government. In the 1960s, Franco’s Opus Dei-linked finance ran Spain’s central bank.

According to several unnamed sources, Opus Dei still has significant influence over the Spanish government, especially the departments of Education, Justice and Banking. It’s also believed to control the Spanish judiciary, with 1/3 of all Spanish judges and prosecutors linked to the group. One former Opus Dei member filmmakers interview blame this influence on Spain’s failure to change its political structure following Franco’s death (1975) or to hold anyone accountable the atrocities committed by his government.

Opus Dei presently has 90,000 members globally: 30,000 in North and South America, 10,000 in Africa, Asia and Oceania, 35,000 in Spain, 4,000 in Italy and 600 in Germany.

Under the organization’s current structure, 2% are priests, 10% are “numeraries” (who live monastic-style lives in Opus Dei residential centers), and the rest “supernumeraries” (allowed to marry and lead private lives).

The lapsed Opus Dei members featured in the film complain bitterly about its cult-like structure, bullying, harsh rules and pressure to recruit new members.

They also talk about the organization’s immense wealth and links with global elites at the highest level. Opus Dei runs numerous schools, universities, hospitals, business schools and foundations, mainly in Spain and the US. The vice president of the European Bank and a Spanish judge on the European Court of Human Rights are allegedly linked to Opus Dei.

The 1983 Mother Jones article Thy Will Be Done  tells a very different story, as does a 2019 article by the  Institute for the Study of Globalization and Covert Politics. The former reports on longstanding collaboration between Opus Dei and Anglo-US intelligence (eg in death squad activity in Latin America). The latter is based on an extensive 1986 Belgian police report linking Opus Dei to high level politicians and officials, western intelligence, elite child trafficking networks.

FDA, CDC Urge All Adults to Get 5th COVID Shot Despite No Safety or Efficacy Data

By  Dr. Joseph Mercola

The emergency authorizations of Pfizer’s and Moderna’s bivalent COVID-19 boosters are based on preliminary test results from only eight mice, and that data hasn’t even been made public.

  • The emergency authorizations of Pfizer’s and Moderna’s bivalent COVID-19 boosters are based on preliminary test results from a grand total of eight mice, and that data hasn’t even been made public.
  • Based on the antibody response in eight mice, the Biden administration has ordered 171 million doses of the two boosters.
  • A reanalysis of data from the Pfizer and Moderna COVID-19 vaccine trials found that combined, the jabs were associated with a risk increase of serious adverse events of special interest at a rate of 12.5 per 10,000 vaccinated. Meanwhile, the risk reduction for COVID-19 hospitalization was only 2.3 per 10,000 participants for Pfizer and 6.4 per 10,000 for Moderna.
  • According to a recent risk-benefit analysis of a third booster for university students, for each COVID-19 hospitalization prevented, the booster will cause 18 to 98 serious adverse events.
  • A number of top officials with the U.S. Food and Drug Administration (FDA), Centers for Disease Control and Prevention (CDC) and the National Institutes of Health reportedly have serious concerns about the direction we’re going in, yet are too afraid to speak out or push back.

On Aug. 31, the FDA authorized the reformulated COVID-19 bivalent booster shots by Moderna and Pfizer — all without the required convening of its Vaccines and Related Biological Products Advisory Committee (VRBPAC), which would typically discuss or vote on the authorization or approval of a new vaccine.

Instead, the FDA pushed the matter before the CDC’s Advisory Committee on Immunization Practices, or ACIP.

ACIP met for eight hours on Sept. 1 and authorized the untested boosters 13-to-1.

CDC director Dr. Rochelle Walensky endorsed the recommendation later that evening.

Pfizer’s new booster, authorized for people age 12 and older, is a bivalent injection targeting Omicron subvariants BA.4 and BA.5, which are the two currently in circulation.

Moderna’s shot, authorized for adults only, aged 18 and older, targets the already extinct Wuhan strain and Omicron subvariant BA.1.

The two bivalent boosters are only available to those who have already received the primary two-dose series and/or a monovalent booster at least two months ago.

Safety and efficacy assumed based on mouse data

As explained in “What They’re Not Telling You About the New mRNA Boosters,” the emergency authorization of these reformulated boosters is based on nothing more than preliminary test results from a grand total of eight mice, and that data hasn’t even been released to the public.

In an Aug. 30, article, Science explained the makeup of the reformulated boosters:

“Both the Pfizer-BioNTech collaboration and Moderna make their vaccines from messenger RNA (mRNA) coding for the spike protein of SARS-CoV-2. The new vaccines are bivalent.”

Half of the mRNA codes for the spike protein of the ancestral virus strain that emerged in Wuhan, China, in late 2019, which is also in the original shots; the other half codes for the spike protein in BA.1 or the one in BA.4 and BA.5, which have identical spikes …

For the BA.4/BA.5 boosters, the companies have submitted animal data.

They have not released those data publicly, although at the June FDA meeting, Pfizer presented preliminary findings in eight mice given BA.4/BA.5 vaccines as their third dose.

Compared with the mice that received the original vaccine as a booster, the animals showed an increased response to all Omicron variants tested: BA.1, BA.2, BA.2.12.1, BA.4, and BA.5.

The companies say clinical trials for the BA.4/BA.5 vaccines will begin next month; they need clinical data both for full approval of the vaccines — their recent submissions are only for emergency use authorization — and to help develop future updates.

Presumably, they will measure recipients’ antibody levels, but not the vaccine’s efficacy against infection or severe disease. Such trials are very expensive and were not done for the BA.1 shot either.”

FDA and CDC rely on assumptions, not actual data 

A key take-home here is that efficacy against infection and severe disease has NEVER been ascertained. Those trials were not done for the original shot, and won’t be done for the reformulated boosters.

Yet the efficacy of these boosters is assumed and declared as having been “proven” based on the original trials.

Talk about a circular argument!

It’s just assumptions piled upon assumptions. Yet, based on the antibody response in eight mice alone, the Biden administration has now ordered 171 million doses of the two boosters.

Let’s not forget that the mice actually did get infected with Omicron, although we don’t know to what degree, since they haven’t released the data. For all we know, the mice may have had a good antibody response, got sick and then dropped dead.

What’s more, the monovalent Pfizer booster authorized for children aged 5 to 11, back in May, was based on the antibody levels of just 67 children.

So, when the FDA claims the original human trials were exhaustive and have conclusively proven the shots are both safe and effective, they’re flat-out lying.

In addition to apparent fraud being committed, and the fact that they eliminated the placebo groups midway, those human trials won’t even be finalized for another two years or so, as all clinical trials require follow-up.

All we have are preliminary analyses, and Freedom of Information Act released documents clearly show Pfizer has been less than transparent about adverse effects, as they mislabeled and dismissed almost all of them.

A reanalysis of data from the Pfizer and Moderna COVID vaccine trials found that, combined, Pfizer and Moderna mRNA COVID-19 jabs were actually associated with a risk increase of serious adverse events of special interest of 12.5 per 10,000 vaccinated.

Meanwhile, the risk reduction for COVID-19 hospitalization was only 2.3 per 10,000 participants for Pfizer and 6.4 per 10,000 for Moderna. So, again, the risk-benefit is crazy lopsided AGAINST the shots.

Repeat boosting can destroy your immune function

Aside from the risk of immediate adverse effects of these experimental gene transfer injections, there’s also the issue of immune destruction through repeat exposure.

A number of scientists have warned that repeated injections appear to be breaking down people’s immune systems.

As noted by independent journalist Rav Avora:

“The European Medicines Agency has warned against the potential adverse immunological effects of repeated boosting every four months.

“As Dr. Marty Makary from Johns Hopkins has noted, recent research shows a ‘reduced immune response against the Omicron strain among people previously infected who then received three COVID vaccine doses compared to a control group that previously had COVID and did not have multiple shots.’

[…]

Public health officials go along to get along

Sadly, a number of top officials within the FDA, CDC and the National Institutes of Health reportedly have serious concerns about the direction we’re going in, yet are too afraid to speak out or push back, so the death toll keeps mounting.

In a July 15 Substack article, Makary and Dr. Tracy Beth Hoeg shared the following:

“The calls and text messages are relentless. On the other end are doctors and scientists at the top levels of the NIH, FDA and CDC. They are variously frustrated, exasperated and alarmed about the direction of the agencies to which they have devoted their careers.

“‘It’s like a horror movie I’m being forced to watch and I can’t close my eyes,’ one senior FDA official lamented. ‘People are getting bad advice and we can’t say anything.’

“That particular FDA doctor was referring to two recent developments inside the agency. First, how, with no solid clinical data, the agency authorized COVID vaccines for infants and toddlers, including those who already had COVID. And second, the fact that just months before, the FDA bypassed their external experts to authorize booster shots for young children …

[…]

Via https://childrenshealthdefense.org/defender/fda-cdc-adults-5th-covid-shot-booster-cola/?eType=EmailBlastContent&eId=d32e72fb-ad2f-4a68-825c-f44b9f7d0111

Physicians Association: FDA Lied About Ivermectin and Should Be Accountable

Clever Journeys

[…]

Most unaware citizens don’t realize the AMA sold out to the Obama Administration [over the insurance lobby boondoggle Obamacare] and less than 14 percent of all American doctors are members.

[…]

Recently the American Association of Physicians and Surgeons (AAPS) filed a motion (a brief) in federal district court in Galveston urging it to allow the lawsuit to proceed against the FDA for its misleading statements against ivermectin.

In Apter v. HHS, a group of physicians sued to hold the FDA, a federal agency within the Department of Health & Human Services (HHS), accountable for its interference with physicians’ ability to treat Covid-19.

“Defendant FDA has improperly exploited misunderstandings about the legality and prevalence of off-label uses of medication, in order to mislead courts, state medical boards, and the public into thinking there is anything improper about off-label prescribing,” AAPS wrote in its amicus brief to the court.

“Not only is off-label prescribing fully proper, legal, and commonplace, but it is also absolutely necessary in order to give effective care to patients,” the brief stated.

Recall that the FDA published multiple statements and sent letters to influential organizations to falsely disparage ivermectin, implying that it was not approved for treating Covid-19.

Many, including courts and state medical boards, were misled by the FDA into thinking that its lack of approval for this treatment meant that ivermectin should not be used to treat Covid-19.

“It has never been proper for the FDA to interfere with that essential part of the practice of medicine, and the FDA knows it,” AAPS informed the court.

The FDA “insisted and continues to insist on interfering with the prescription of this safe medication by physicians in treating Covid-19,” AAPS added.

[…]

AAPS General Counsel Andrew Schlafly pointed out to the court that the FDA “has engaged in a campaign of interference with the proper use by physicians of ivermectin, which has long been approved as fully safe for human use.”

He alerted the court that once the FDA approves a medication as safe, then physicians have full authority to prescribe it to treat any illness, particularly a novel virus like Covid-19.

In August 2022, AAPS filed similar motions in federal Southern District of Texas, against three medical special boards for their threatened retaliation against physicians who speak out on matters of public concern.

“Our freedoms depend on the ability of physicians and all Americans to speak out on important issues of our day,” said Andrew Schlafly, who filed this lawsuit. “Entities holding monopolies over board certification should not be retaliating against good physicians.”

This new lawsuit asserts that “Defendants wrongly misuse their authority in a politically partisan manner to chill speech critical of positions taken by Dr. Anthony Fauci, lockdowns, mask mandates, Covid vaccines and even abortion.”

This Complaint seeks injunctive and declaratory relief against several specialty Board Defendants that hold monopolies over board certification, and against the federal government for its newly created Disinformation Governance Board.

“Although only official state medical boards have the proper authority to regulate the practice of medicine, certifications by the Board Defendants constitute a de facto essential credential for practicing in most hospitals or participating in most networks,” this lawsuit asserts. “By threatening to revoke board certification of physicians, the Board Defendants improperly chill speech by physicians without the political accountability of official state medical boards,” this Complaint adds.

The Board Defendants are the:

🔹American Board of Internal Medicine

🔹American Board of Obstetrics & Gynecology

🔹American Board of Family Medicine.

Each of these entities, which hold monopolies over board certification in their specialties, have declared their plans to discipline physicians who speak out.

“Criticizing Dr. Anthony Fauci should not be a basis for retaliating against a physician for speaking his mind,” Andrew Schlafly states. The lawsuit points out that many Republican senators properly rebuked Dr. Fauci for his statements that “I represent science” and that those who criticize him “are really criticizing science.”

[…]

Via https://cleverjourneys.com/2022/10/07/fda-lied-about-ivermectin-and-should-be-accountable-in-court-says-physicians-association/

Negative Vaccine Efficacy Keeps Rearing Its Ugly Head: Now Kaiser Admits It

By Dr Meryl Nass

Kaiser Permanente is both an insurance company and a healthcare provider company. It negotiates with employers once a year to set its health insurance rates. I wonder if Kaiser started getting worried at the amount of excess illness it was seeing. Once people are too sick to work, they lose their health insurance. But what if they are somewhat sick, but keep working? What if their chronic, mystery illnesses consume a larger amount of medical care than Kaiser bargained for? Kaiser might be willing to do a little truth-telling as it tries to calculate who is going to pay for this unexpected hit, which presumably did not stop in 2021 but continues apace.

Here is Daniel Horowitz’ article. Here is the Kaiser preprint. On page 30, you can see the following table, which shows how well 3 shots worked for over 120,000 Kaiser enrollees who were tested for COVID during Omicron. Kaiser did something unusual: it actually sequenced 16,418 positive COVID samples to determine the Omicron subvariant with which the enrollees were infected.

What it found was that for 4 out of 5 Omicron subvariants by 150 days (5 months) post shot, efficacy had fallen into negative territory, and Kaiser’s thrice-vaccinated enrollees were more likely to get COVID than the unvaccinated.

VE stands for vaccine efficacy (effectiveness). The vertical lines are at the ZERO efficacy mark. You can see how efficacy drops quickly from the 14-30 days post-shot (which is the brief honeymoon period when the shots actually work), lower at 1-3 months, lower still at 3-5 months, and after that you are screwed.

All the dots to the left of the line show negative efficacy—that is when you become more prone to getting a COVID infection. After 5 months, people were more likely to get a case of Omicron BA.2, BA.2.12.1, BA.4 and BA.5 if they had been vaccinated. Each gray bar starts a new subvariant.

There are 2 graphs. The one on the left compares the triple-vaxxed to the unvaxxed, while the graph on the right compares the triple-vaxxed to the double-vaxxed.

Even worse for the boosted, it seems that those with 3 shots are at more risk of COVID after 5 months than those who only got two shots (this is on the right side of the graph). So please stop. It gets worse with each jab.

Via https://merylnass.substack.com/p/negative-vaccine-efficacy-keeps-rearing/

Now, All of You Are Azov”: Ukrainian ‘Neo-Nazis’ Tour U.S.

After meeting with at least 50 members of Congress, soldiers of the neo-Nazi Azov Regiment toured the US to auction off swastika-inspired patches and lobby for an end to restrictions on US arms and training.

Moss Robeson

360° Internationalist

From top to bottom: Rep. Pete Sessions, Sen. Todd Young, and Sen. Rick Scott meeting with Giorgi Kuparashvili (red), Vladyslav Zhaivoronok (white), and Artur Lypka (yellow) from the Azov Regiment.

[…]

[…]

In his closing remarks, Giorgi Kuparashvili appeared to take aim at his least two favorite members of Congress: Ro Khanna, a liberal Democrat from Silicon Valley, thanks to whom Congress curtailed U.S. support for the Azov Regiment in 2018, and Max Rose, a former Congressman and right-wing Democrat from Staten Island, who called on the State Department to label the Azov Regiment a “Foreign Terrorist Organization” in 2020.

“From year ’14, ’15, ’16, until today,” claimed Kuparashvili, “there is a bill which, I don’t remember the name, but the Congressman who lobbied, I don’t know how… He left Congress a couple years ago, he initiated to put the Azov as a restriction in a bill. This week, we talked to all the Congressmen and Senators, everybody understands, because when you bring the bill to Congress, they have to read it. Unfortunately, nobody read it, so they approved it again.”

Evolution of the Azov swastika. The “Black Sun” confirms that this is a neo-Nazi symbol.

[…]

Via https://libya360.wordpress.com/2022/10/06/now-all-of-you-are-azov-ukrainian-neo-nazis-tour-u-s/

Is the US Blood Supply Tainted

Despite reports that COVID-19 vaccines cause blood abnormalities, the American Red Cross and the U.S. Food and Drug Administration continue to brush off concerns that the massive vaccine campaign may have contaminated the country’s blood supply.

As of mid-September, the Vaccine Adverse Event Reporting System (VAERS) — notorious for capturing only a minuscule proportion of adverse events — had received notification of more than 43,000 blood clotting disorders, including acute-onset problems in young children.

Clotting disorders make the blood clot “too easily,” generating clots that can travel through the bloodstream and increase the risk of heart attacks and strokes, among other potential complications.

Funeral directors and embalmers in the U.S. and U.K. have gone public with shocking descriptions of highly unusual blood clots in up to 85% of the bodies coming under their care — a “massive increase” compared to pre-COVID-19 vaccine times when ordinary-looking clots might be found in 5% to 10% of the deceased.

“In all my years of embalming, we would run across clots from time to time,” said Richard Hirschman, an experienced funeral director in Alabama, “but since May last year [2021], something about the blood has changed. It’s not normal. It’s drastic.”

The rampant clotting and the clots’ disturbing sci-fi appearance — “long fibrous entities that can completely block a vein or artery,” which Hirschman likens to calamari, rubber bands, spaghetti, worms or parasites — are just some of the concerns prompting questions about blood supply safety.

No ‘safety risks?’

About 55% of blood is plasma — which, among other functions, supplies proteins “for blood clotting and immunity” — with the remaining 45% consisting of red blood cells, white blood cells and platelets suspended in the plasma.

Depending on their blood type, individuals who give blood can choose to donate whole blood, plasma or platelets, or they can make a “Power Red” donation (a “concentrated dose” of red blood cells).

The American Red Cross says it will not accept blood from someone whose blood “does not clot normally,” but — following guidance from the same branch of the FDA that oversees vaccines — welcomes immediate donations from anyone who received one of the mRNA or other COVID-19 vaccines available in the U.S., as long as the person says he is “symptom-free and feeling well.”

The Red Cross claims to be independent but openly celebrates its “special relationship” with the federal government — a relationship that includes periodic appropriations and contracts.

In a recent tweet directed at potential blood transfusion recipients, the Red Cross clarified:

The tweet generated numerous responses from the public accusing the Red Cross of disseminating “misinformation” and directing the organization’s attention to peer-reviewed publications contradicting its languid attitude.

In one of the most alarming studies, published in August in the International Journal of Vaccine Theory, Practice, and Research, Italian surgeons described atypical clumping of red blood cells and the presence of “extraordinarily anomalous structures and substances” of “various shapes and sizes of unclear origin” in over 94% of symptomatic, COVID-19-vaccinated individuals whose blood they examined.

The 1,006 study participants, ranging in age from 15 to 85, received a first (14%), second (45%) or third (41%) dose of a Pfizer or Moderna mRNA vaccine about a month before the analysis of their blood.

Pointing to other studies that found foreign materials in the blood of COVID-19 vaccine recipients and in COVID-19 vaccine vials — materials “that the CDC [Centers for Disease Control and Prevention] and the many promoters of the experimental injections claimed were not in them at all” — the Italian authors concluded the vaccine-induced blood alterations were “likely … to be involved in producing the coagulation disorders commonly reported after anti-COVID injections.”

Putting the matter even more plainly, they stated:

“[S]uch abrupt changes as we have documented in the peripheral blood profile of 948 patients have never been observed after inoculation by any vaccines in the past according to our clinical experience. The sudden transition … from a state of perfect normalcy to a pathological one … is unprecedented. …

“In our collective experience, and in our shared professional opinion, the large quantity of particles in the blood of mRNA injection recipients is incompatible with normal blood flow especially at the level of the capillaries.”

Another study by Romanian researchers, sent to the Red Cross by the tweeting public, not only reported that Pfizer’s “vaccine-associated synthetic mRNA persists in systemic circulation for at least 2 weeks” but also noted, “extended plasma clearance times compared to estimates presented by mRNA vaccine manufacturers.”

Meanwhile, a case report from Germany presenting autopsy results for a man who died after receiving three “gene-based” COVID-19 vaccine doses (one AstraZeneca, two Pfizer) over a seven-month period conclusively revealed the presence of COVID-19 vaccine spike protein in both brain and heart — and particularly in small blood vessel cells.

These and other studies may be why members of the public like “Mary” incredulously tweeted back to the Red Cross, “Are you kidding? There is proof it enters other body cells like the heart, causing myocarditis; how do you think it gets to the heart from the injection site???”

The FDA has refused to release autopsy results in its possession for people who died following COVID-19 vaccination.

 

 

Out, damned clot

As early as May 2021, vaccine researchers were disclosing the “unexpected” entry into the bloodstream of the vaccines’ synthetic spike protein, while other pharmaceutical industry consultants admitted, “Some of the vaccine dose is going to make it into the bloodstream, of course.”

Around the same time, figures like Canadian physician Dr. Charles Hoffe were warning that technologies like CT scans and MRIs, which can identify large blood clots, would not find the “microscopic” clots affecting many of the COVID-19-vaccinated, who might “have no idea they are even having these microscopic blood clots.”

Hoffe was able to ascertain the widespread presence of micro-blood clots in his mRNA-vaccinated patient population using D-dimer tests that look for protein fragments associated with clots.

The Canadian doctor also cautioned that when blood clots damage the brain, spinal cord, heart or lungs, “those tissues … are permanently damaged.”

A year after these admissions, in May 2022, the FDA finally acknowledged the risk of “potentially life-threatening blood clots” in recipients of the Janssen/Johnson & Johnson (J&J) COVID-19 vaccine.

The European Medicines Agency (EMA) issued similar advisories about AstraZeneca’s COVID-19 vaccine.

[…]

Is the U.S. Blood Supply Tainted?

 

Decoding Putin’s So-Called Nuclear Threat

Dmitry Orlov

This phrase currently yields about 6,590,000 results on Google, so it must be real—or is it not? It is not. But apparently figures most authoritative have concocted a narrative where Putin, in desperation over the loss of Krasny Liman, a railroad junction in the Kramatorsk district of Donetsk People’s Republic, which as of yesterday is part of Russian Federation, will get all emotional and attack the Ukrainians using tactical nuclear weapons. Since this narrative is bogus, there must be something else going on, such as a false flag being planned by the US. Let’s tease this narrative apart and see where it leads.

If you have never heard of Krasny Liman, you are hereby forgiven for this bit of geographic ignorance. It is only notable for two things: a rail junction and the fact that the Russians recently decided to pull back from it while inflicting horrific losses on the attacking Ukrainians. As far as battlefield losses, the 10:1 ratio (10 dead Ukrainians for every dead Russian) seems to be holding steady.

Given that Russia’s population is 4 times larger and that Russia makes all of its own weapons while the Ukraine is forced to rely on the kindness of strangers, Russian victory on the battlefield is entirely assured. Krasny Liman and its majestic railway station will be retaken in due course, because it now happens to be on Russian territory, but there is no reason to rush. What’s happening now in Novorossiya (what the region was called when it was first settled by Russians, displacing wandering nomadic remnants of Genghis Khan’s empire) is an anti-terrorist operation, the Ukrainians and their Western supporters being the terrorists. The Russian troops are slowly grinding their way to victory, defined as liberating Novorossiya from the Ukrainian forces and foreign mercenaries, which are, since no war has ever been officially declared, illegal combatants—i.e., terrorists.

In case you wish to challenge these definitions, let’s add some perfectly boring legal facts. Novorossiya (currently including Donesk, Lugansk, Kherson and Zaporozhye, and eventually to include, at a minimum, Nikolaev, Odessa, Kharkov and Dnepropetrovsk) recently voted in a referendum on whether to join the Russian Federation. The numbers were overwhelmingly in favor.

A referendum is a legal instrument of direct democracy by which a people make their sovereign will known to the world, enshrined in Article 1 of the UN Charter as: “the principle of equal rights and self-determination of peoples.” This is international law; there is also a lot of he-said-she-said: the regime in Kiev claims that these regions are separatists; the would-be separatists rejoin that the Kiev regime is itself illegal, having been installed by Americans in an unconstitutional, violent coup d’état in 2014. But as far as Moscow is concerned Novorossiya is part of Russia because its people have so chosen while the Ukrainians and various mercenaries on its territory are terrorists to be exterminated or expelled.

You may wonder why such legalities are important here, given that shells are exploding and people are dying, and you may feel compelled to run around with your hair on fire in a futile attempt to make them stop. Well, good luck with that, but to the Russians questions of legality in international relations are of paramount importance.

Some 85% of the world’s population that is not part of the collective West sees Russia as a valuable deterrent against predatory, neo-colonialist Western practices (with its “rules-based international order” where nobody has ever seen, never mind ratified, this imaginary compendium of rules). Russia is eager to position itself as a trustworthy partner acting within a mutually acceptable legal framework. The success of international organizations such as SCO and BRICS, which many nations wish to join, testifies to the effectiveness of this approach. In contrast, the US is seen as an increasingly rudderless, internally conflicted renegade nation and the EU as a gaggle of its feckless minions.

What Putin Actually Said

These preliminaries out of the way, let us now consider the nature of “Putin’s nuclear threat.” The brilliant idea for concocting this false narrative came from Putin himself who, during his speech on the occasion of accepting Novorossiya into the Russian Federation, said this:

Translation: “I wish to remind those who allow themselves to make such statements in relation to Russia that our country also possesses various offensive weapons, certain components of which are more modern than those of NATO countries. And in case of threats to the territorial integrity of our country, for the defense of Russia and of our people, we will most definitely make use of all means in our possession.”

Putin did not explicitly mention nuclear weapons, although he did warn against nuclear blackmail and said, ominously, that “the wind rose can point in any direction,” implying that nuclear fallout can spread anywhere the wind blows.

And this was enough to send Western mass media into high dudgeon, causing it to hyperventilate continuously while spewing out an endless stream of verbiage on “Putin’s nuclear threat.” But it’s not a threat—it’s a promise, and for details one should look to Russia’s Nuclear Doctrine which spells out the exact conditions under which Russia’s nuclear deterrent will be employed: no first use, and to be used only in response to an existential threat. The temporary tactical retreat from Krasny Liman with its lovely railroad station is not an existential threat by any stretch of the imagination; that, plus the “no first use” stipulation in Russia’s nuclear doctrine, guarantee that Russia will not use a nuclear weapon in response.

If that’s the case, then what are we to read into “Putin’s nuclear threat” beyond an excuse to hyperventilate and rant about Russia-Russia-Russia, to distract from the now $31 trillion US federal debt and other looming disasters? The US has exhibited a pronounced penchant for false flags (9/11, where 3 skyscrapers—WTC 1, 2 and 7—were, if you are gullible, knocked down using 2 Boeings) and an equally pronounced penchant for using nuclear explosives for political ends (Hiroshima, Nagasaki, and then Fukushima, where a nuclear depth charge was used to trigger a tsunami that all but shut down Japan’s nuclear power industry). Perhaps the plan is to combine the two ingredients by nuking Kiev and then attempting to pin the blame on Russia. Given that the US just blew up Nord Stream pipelines with barely a reprimand, why wouldn’t it just keep its terrorist strikes coming?

[…]

US government stocks up on $300m worth of radiation sickness drugs

 

Descubre todo lo relacionado sobre el Romiplostim y más

 

By Caitlin Tilley

Daily Mail

  • The US Government makes its first purchase of Nplate for ‘nuclear emergencies’
  • The drug treats radiation sickness by stopping life-threatening bleeding
  • Putin’s nuclear warning did not spur the purchase, the Government said

The US has stocked up on radiation sickness drugs just weeks after Vladimir Putin threatened to use nuclear weapons against the West.

Officials said the deal — worth $290million — was ‘part of ongoing work’ and ‘has not been accelerated’ by the Kremlin leader’s escalating rhetoric.

The US Health and Human Services (HHS) – whose motto is to ‘improve the health, safety, and well-being of America – announced the purchase of romiplostim Tuesday.

Sold under the brand name Nplate, it is used to reduce bleeding caused by acute radiation syndrome (ARS), also known as radiation sickness.

Putin issued a chilling warning late last month that he was prepared to use Russia’s nuclear arsenal to protect Ukrainian territory annexed after sham referendums.

But the US Health and Human Services (HHS) said the drug order was ‘part of ongoing work’ and ‘has not been accelerated’ by Putin’s warning.

However, the timing will likely raise questions given that this is the first time the US Government has bought Nplate.

It is unclear how many doses the order covers, but the drug normally fetches between $1,000 and $2,500 per dose.

The US Government began stocking up on anti-radiation drug Nplate after Vladimir Putin threatened to nuke the West over Ukraine

What is radiation sickness? 

ARS, known commonly as radiation sickness, is an illness that can happen when a person is exposed to high levels of radiation, typically over a short time period.

The initial symptoms of ARS include nausea, vomiting, headache, and diarrhea.

But the way in which radiation affects our bodies is not fully understood.

Symptoms can start within minutes to days after the exposure, can last for minutes up to several days, and may come and go.

After the initial symptoms, a person usually looks and feels healthy for a period of time, but will likely suffer further symptoms at varying degrees of severity, depending on the dose.

These symptoms include loss of appetite, fatigue, fever, nausea, vomiting, diarrhea, and possibly even seizures and coma.

This seriously ill stage may last from a few hours up to several months.

Absorbing high doses of radiation can also dramatically increase the likelihood of developing cancers and other chronic illnesses years down the line.

Besides the two workers who were killed instantly in the initial explosion at Chernobyl in 1986, a total of 134 plant staff and emergency workers experienced ARS in the days following the accident, of which 28 died.

Radiation sickness occurs when a person’s whole body is exposed to a high dose of penetrating radiation, which reaches internal organs in seconds.

It can leave people with low platelet counts, causing impaired blood clotting and leading to ‘uncontrolled and life-threatening bleeding’.

Nplate – made by California pharmaceutical company Amgen – stems bleeding by stimulating the body’s production of platelets, and can be used in both adults and children.

It can also be used to treat patients with immune thrombocytopenia, a blood condition causing low platelet counts.

The HHS said the buying of the drug was due to its ‘long-standing, ongoing efforts to be better prepared to save lives following radiological and nuclear emergencies’ and not a response to Russia’s president.

‘This is part of our ongoing work for preparedness and radiological security. It has not been accelerated by the situation in Ukraine,’ it added in a statement.

The US has kept a supply of Leukine, another drug which treats ARS, since 2013, in case of a nuclear event.

As well as Leukine and Nplate, two other drugs are approved by the US Food and Drug Administration to treat acute radiation exposure – Amgen’s Neupogen and Neulasta.

Nplate is approved for use in Europe and the UK to treat immune thrombocytopenia, but not injuries resulting from radiation exposure.

[…]

Via https://www.dailymail.co.uk/health/article-11286835/US-buys-290m-worth-radiation-sickness-drugs-amid-Russias-nuclear-threat.html