The Most Revolutionary Act

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

The Most Revolutionary Act
Unknown's avatar

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.

Social Structure in Medieval Ireland

Episode 17 Celtic Women, Families and Social Structure

The Celtic World

Dr Jennifer Paxton (2018)

Film Review

Paxton cites historian Daniel Binchy in describing medieval Irish society (the same mostly applies to medieval Wales) as tribal, rural, hierarchical and familial.

Tribal

Medieval Ireland had at least 100 kings at any one time. Each king ruled a kinship group of a few thousand people.

Rural

There were no cities in early Ireland, and its five provinces (Ulster, Connacht, Meath, Leinster and Munster) were purely geographic designations with no political authority.

Hierarchical

Membership of the nobility required having clients dependent on you. There were two kinds of clientship, free and base. A free client paid higher rent and could end the clientship at will. He was required to provide some labor services for the lord (or get one of his own clients to provide it) and to participate in his war band. A base client received land and a few cattle in return for labor services, diary products, grain, malt and meat he paid as rent. He also helped dig the lord’s grave, patrolled border lands and participated in expeditions to weaker territories. He had to pay a fee to leave a base clientship.

Aside from the nobility, there were learned classes consisting of poets, lawyers and (prior to Christianity) Druids. Unlike lawyers in rest of Europe, Irish lawyers remained independent of the church. Like poets, they were allowed free passage between warring kingdoms.

The honor price for killing or maiming someone was based on their wealth and occupation. It was calculated in “cumal,” with one cumal equal to one slave girl or three cows. Kings, bishops and high poets had the highest honor price, followed by nobles and learned classes, followed by farmers. Slaves, who were regarded as property, had no honor price. Wealthy Irish could also file suit if some maimed or insulted them.

Irish kings weren’t lawgivers in medieval Ireland, where the legal system relied mainly on common law, judges and lawyers. However many legal texts, recopied many times, survive from the Middle Ages. One law that was extremely frustrating for British colonizers was “distraint,” a legal method of forcing someone to comply with a judge’s order by simply helping yourself to the loser’s cattle.* It was also acceptable to pressure someone into complying by fasting on their doorstep.**

Familial

In Ireland, all property transactions had to be approved by everyone descended from the same great grandfather. A family could be artificially extended by adopting foster children, and women joined joined their husband’s kinship group. Legal marriage wasn’t required so long as a woman’s partner acknowledged paternity of her offspring. Owing to the absence of a criminal legal system, it was up to the kinship group to file suit on behalf of a murdered family member.

Early Ireland was an extremely patriarchal society although Irish women had somewhat more rights than those of Britain or Europe.

  • In both Wales and Ireland, women could initiate divorce and couples could form temporary unions that could be dissolved by mutual consent
  • There were women poets and doctors in medieval Ireland.
  • Some women were allowed to own property, but in most jurisdictions it was forbidden.
  • There was considerable evidence of polygamy among high status men.
  • Slave girls were often sexually exploited by their masters.
  • If a woman dissolved her marriage, she returned to her father’s guardianship.

*This was necessary in a society where there was no infrastructure to enforce laws.

**This tradition gave rise to hunger strikes as a weapon in the fight for Irish independence in the early 20th century and during the “troubles” in Northern Ireland.

Film can be viewed free with a library card on Kanopy.

https://pukeariki.kanopy.com/en/pukeariki/video/5701024/5701054

‘Data Are Unequivocal’: Florida Surgeon General Fires Back at FDA, CDC on COVID Vaccines

Claiming that a “lack of transparency only harms Americans’ faith in science,” Florida Surgeon General Joseph Ladapo, M.D., Ph.D., this week called on the nation’s top public health officials to “publicly” explain 12 key issues related to the COVID-19 vaccine rollout.

In a letter sent Wednesday to U.S. Food and Drug Administration (FDA) Commissioner Robert Califf and Centers for Disease Control and Prevention (CDC) Director Rochelle Walensky, Ladapo said:

“Your ongoing decision to ignore many of the risks associated with mRNA COVID-19 vaccines alongside your efforts to manipulate the public into thinking they are harmless, have resulted in a deep distrust in the American health care system.

“Beginning with Operation Warp Speed, and possibly to be continued with an additional $5 billion investment in Project NextGen, the federal government has relentlessly forced a premature vaccine into the arms of the American people with little to no concern for the serious adverse ramifications.”

Ladapo said the “data are unequivocal: After the COVID-19 vaccine rollout, the Vaccine Adverse Events Reporting System (VAERS) reporting increased by 1,700%, including a 4,400% increase in life-threatening conditions.”

Ladapo listed 12 points of data and demanded the health officials “publicly” explain their decision-making process around those data.

Commenting on the letter, blogger Igor Chudov said the surgeon general asks “all the right questions” about COVID-19 vaccines — and exposes the FDA and the CDC as “charlatans” engaging in “medical quackery.”

Chudov summarized Ladapo’s questions:

  • Why were randomized clinical trials not conducted for “Covid boosters” (such trials were necessary to establish that they are safe and effective)
  • Why did the FDA ignore many subclinical myocarditis reports and allow Pfizer to postpone its report on subclinical myocarditis?
  • Why were vaccine side effects intentionally ignored in V-Safe?
  • Why did the FDA allow Pfizer to hide the results of its clinical trial of Covid vaccines in pregnant women, that ended in 2022?
  • Why are the FDA and the CDC hiding negative effectiveness of Covid vaccines?

Wednesday’s letter is the latest in an ongoing exchange between Florida’s surgeon general and the agencies’ top officials that began when Ladapo, in a Feb. 15 letter, expressed concern about the adverse effects of mRNA COVID-19 vaccines and asked FDA and CDC officials for greater transparency in publicly acknowledging these effects.

The letter corresponded with a health alert Ladapo issued that same day to the Florida healthcare sector and the public warning that mRNA COVID-19 vaccines caused a “substantial increase” in reports of adverse events in Florida.

The letter and health alert summarized the substantial increase in VAERS reports in Florida after the COVID-19 vaccine rollout, including for life-threatening conditions.

On March 10, Califf and Walensky responded to the letter and alert by saying their agencies were monitoring data for potential risks and that Ladapo had focused his letter on “rare” events.

According to Wall Street Journal writer Allysia Finley, Califf and Walenky in their response resorted to “personal attacks” on Ladapo and “ignored the science” he presented.

On Wednesday, Ladapo fired back at Califf and Walensky in a tweet:

In October 2022, Florida became the first state to recommend against mRNA COVID-19 vaccination of children and men up to age 39.

[…]

Via https://childrenshealthdefense.org/defender/joseph-ladapo-cdc-fda-answers-covid-vaccines/?utm_id=20230511

Leading OB-GYN Group Accepted $11 Million From CDC to Push COVID Shots on Pregnant Women

The Centers for Disease Control and Prevention (CDC) bankrolled the American College of Obstetricians and Gynecologists (ACOG) to the tune of $11 million to promote COVID-19 vaccination as “safe and effective” for pregnant women, according to an investigation published this week by attorney Maggie Thorp.

Documents obtained by Thorp through a Freedom of Information Act (FOIA) request revealed that the CDC and ACOG entered into multiple “cooperative agreements” to carry out work largely designed and controlled by the CDC and contingent on ACOG’s adherence to the CDC’s policies on COVID-19 infection and control.

ACOG is the “premier” professional membership organization for obstetricians and gynecologists with more than 60,000 members across the Americas, its website reports.

Broadly, the grants supported the development of social media communications strategies, toolkits supporting “effective COVID-19 vaccination conversations” between doctors and patients, and the hiring of a global public health communications firm, APCO Worldwide, to produce various communications materials.

According to Thorp, from December 2020, when the vaccines came on the market, through July 21, 2021, ACOG held a neutral position on vaccination during pregnancy, recommending that pregnant women “be free to make their own decision regarding COVID-19 vaccination.”

But that recommendation “abruptly changed on July 30, 2020,” Thorp said, to recommend vaccination for pregnant women.

Today, ACOG “recommends that all eligible persons aged 6 months and older, including pregnant and lactating individuals, receive a COVID-19 vaccine or vaccine series,” and a booster.

The money for the grants comes from COVID-19-related federal funding opportunities, such as the Coronavirus Preparedness and Response Supplemental Appropriations Act and the CARES Act, according to the grant documents.

Grant recipients, and any “flow-down” organizations they may award money from these grants to, must comply with “existing and future directives and guidance” from the U.S. Department of Health and Human Services (HHS), the CDC’s parent organization, regarding the control and spread of COVID-19.

That also includes sharing any data collected in grant-funded activities, including COVID-19 testing data, with the CDC.

‘Vast, covert government operation unleashed … at the height of our fear and isolation’

This CDC-ACOG collaboration forms part of the CDC’s and HHS’ strategic approach to COVID-19 vaccination encapsulated in its “We Can Do This” public education campaign.

Through the campaign, HHS and CDC sought in their own words to “motivate behavior change,” through strategic messaging, often developed by public relations firms, using “market research, key messages, partnerships and outreach, paid and earned media, and sample creative,” across all areas of people’s lives.

With $3 billion in federal funding from the Biden White House for states to distribute to local agencies and nonprofits and hundreds of millions of dollars in direct grants to medical associations and nonprofits, the HHS and CDC sought to train and fund “trusted messengers” such as teachers, religious leaders, social media influencers, community leaders and members and others, who would deliver the CDC’s message, but without the CDC’s brand.

This also included, Thorp wrote, creating the COVID-19 Community Corps — reminiscent of Theodore Roosevelt’s Civilian Conservation Corps work relief program that put millions to work during the Great Depression — described as “a nationwide, grassroots network of local voices people know and trust to encourage Americans to get vaccinated.”

The COVID-19 Community Corps targeted “vaccine-hesitant” populations, including pregnant women, Thorp’s investigation revealed.

Thorp called the “trusted messengers” the CDC’s “Trojan horses” that used interpersonal relations of trust to enter into people’s personal lives and communicate the CDC’s message.

[…]

CDC, ACOG had data showing risks to pregnant women but pushed vaccines anyway

Dr. James Thorp, board-certified obstetrician-gynecologist and maternal-fetal medicine physician who also contributed to the research, told The Defender he thought it was particularly troubling that regulatory agencies and medical associations were aware of risks to pregnant women and yet pushed the vaccines.

Red flags in Pfizer’s data regarding the possible adverse effects of the vaccines for pregnant women were leaked in 2021, according to James Thorp. He said:

“They had the data. So they must have said, ‘Okay, we’re not going to be transparent with the data. We’re going to denigrate their data and our own data (VAERS and Pfizer 5.3.6), and suggest that — all the morbidity and danger signals and mortality, we’re just gonna brush it off.

‘And we’re going to spend $13 billion on psychological operations, fifth-generation war, to convince everybody in the world that it is safe and effective and necessary in the most vulnerable populations: pregnant women, pre-born and newborn babies, and the next most vulnerable population, children.’”

“It’s one thing when you’re trying to pull off this mass marketing campaign using marketing tactics that companies have been using for years to sell regular products such as candies, foods or clothing,” James Thorp said, “But they’re doing this with untested gene therapy products in pregnancy.

He added:

“The Department of Defense, HHS, CDC, ACOG, the Society for Maternal-Fetal Medicine, the American Board of Obstetrics and Gynecology and others are unequivocally attempting to abolish a highly-revered, God-ordained, gold standard doctrine that has been memorialized and honored and has withstood the scientific test of time over millennia: Never give novel substances in pregnancy without short-term and long-term outcome studies in the offspring.

[…]

Maggie Thorp added that if the HHS and CDC were directing people’s behavior as they explicitly sought to through these grants, “Then there is no informed consent happening.”

CDC participated in ‘all aspects of carrying out’ ACOG grants

The cooperative agreements stipulated by the CDC would have “substantial programmatic involvement” after the grant is awarded. Above and beyond the monitoring and review typical of CDC grants, in these cases, CDC program staff would also “assist, coordinate, or participate in all aspects of carrying out the awards.”

Maggie Thorp identified the grants on USAspending.gov and got the details through a FOIA request, but the response was heavily redacted.

One grant set an April 30, 2021, deadline — which she noted was prior to when ACOG publicly recommended vaccination for pregnant women — to create an “Emergency Resource Request Tool (ERR)” to target OB-GYNs “and the women they serve.”

The purpose of the ERR tools changed over time. By March 2022, they were focused on “developing, maintaining, and promoting tools to combat misinformation on COVID-19, which has emerged as a significant barrier to the uptake of vaccination during pregnancy,” Maggie Thorp quoted from the FOIA documents.

Another ERR tool involved developing some type of communications tool — it is unclear from the redacted FOIA specifically what it entailed — that would be piloted by ACOG and the American Academy of Pediatrics, which is another COVID-19 Community Corps member.

Another $300,000 went to a contract with APCO Worldwide, “a global public health communication vendor” to develop a COVID-19 Social Media Communications toolkit to provide “key messaging and talking points around COVID-19 for dissemination,” to create virtual training sessions for ACOG members, and to develop a podcast series for members to keep them up-to-date on CDC recommendations.

In October 2021, a multi-year grant addressing breast cancer and other maternal health issues was revised to direct $3,000,000 toward “Engaging Women’s Health Care Providers for Effective COVID-19 Vaccine Conversations” and $300,000 toward “Improving Ob/Gyn’s Ability to support COVID-19 Vaccination, Mental Health, Social Support.”

That grant was renewed in 2022, with $2 million toward the “Vaccines Conversations” effort.

Rather than coordinate plans and messages with its membership, ACOG, in exchange for this grant money, committed to working closely with the CDC, sharing information and efforts, discussing recommendations and meeting frequently to “ensure that recommendations are aligned between the two organizations.”

Clinicians told to document vaccine refusal in medical records

Specific details of the grants were heavily redacted in the FOIA documents Maggie Thorp received. But she pointed to ACOG’s website for evidence of the grant work. On one page, the organization offers a “Conversation Guide” with messaging language on the vaccine for physicians.

The key advice to clinicians is that all pregnant women should be vaccinated and boosted at any time in their pregnancy, that those who refuse should have it documented in their record, and that follow-up visits should focus on continuing to try to convince them to accept vaccination.

[…]

The website also lists “key messages” that should be communicated to pregnant women, including that COVID-19 is quite dangerous for pregnant women, and that there “may be” increased risk of stillbirth. But, the “messaging list” says, there are no “maternal or fetal” effects associated with the COVID-19 vaccines, proven by a “growing body of evidence.”

These recommended talking points remain on ACOG’s website today.

The CDC promoted and continues to promote, the COVID-19 vaccines as safe for pregnant women despite recent revelations that as early as January 2021, the U.S. regulatory agencies were aware of indications in Pfizer’s own data that the vaccines pose serious risks for pregnant women.

[…]

Via https://childrenshealthdefense.org/defender/obgyn-cdc-covid-vaccine-pregnant/

Supreme Court Declares Imran Khan’s Arrest Unlawful

Pegasus spyware | Supreme Court to take up report on Pegasus spyware ...

The Supreme Court (SC) on Thursday termed PTI Chairman Imran Khan’s arrest in the Al-Qadir Trust case “unlawful” and directed him to appear before the Islamabad High Court (IHC) tomorrow (Friday).

“The manner of execution of the arrest warrant issued by the Chairman, National Accountability Bureau (NAB) dated 01.05.2023 in the Al-Qadir Trust case within the premises of the Islamabad High Court against the petitioner is invalid and unlawful,” the ruling said.

Imran was whisked away from the IHC premises by paramilitary forces on Tuesday, leading to violent protests across the country. The PTI chief had immediately approached the high court for release but it had declared his arrest legal.

The former premier’s lawyer, Barrister Ali Zafar, then petitioned the SC on his behalf for Imran’s release.

Earlier today, a three-judge bench comprising the Chief Justice of Pakistan (CJP) Umar Ata Bandial, Justice Muhammad Ali Mazhar and Justice Athar Minallah took up Imran’s petition and had directed NAB to present him before court.Subsequently, the PTI chief was presented in court amid tight security a little after 5:45pm. A Dawn.com correspondent present at the scene said that the former prime minister was taken inside the SC via the judges’ gate.

In the written verdict, a copy of which is available with Dawn.com, the top court said that the execution of NAB’s arrest warrant violated the petitioner’s right of access to justice and “the sanctity and safety of the court as he had already surrendered to the court for seeking judicial relief against the action taken by NAB in the Al-Qadir Trust case”.

In this regard, it highlighted that the fundamental rights of the petitioner under Articles 4, 9, 10-A and 14 of the Constitution had been infringed.

“The petitioner is directed to be produced before the Islamabad High Court tomorrow i.e. 12.05.2023 at 11am for hearing of his Writ Petition filed to challenge the NAB action against him in the Al-Qadir Trust case.

“The NAB authorities and the ICT Police shall ensure foolproof security to the petitioner until his production in the Islamabad High Court in this regard,” the court order stated.

The apex court also directed the registrar of the IHC to place the matter before IHC CJ Justice Aamer Farooq for the constitution of a bench to hear the case.

It went on to say that to secure Imran’s security until his appearance at the IHC tomorrow, he “shall remain in the premises where he is presently retained in police custody, namely, the Police Lines Guest House, H-11, Islamabad (Police Guest House)”.

[…]

Imran asks supporters to remain peaceful

During the hearing today, Imran said that no harm should be caused to the country and asked his supporters to remain peaceful. “We only want elections in the country,” he maintained.

The PTI chief stated that he was told by his lawyers a day earlier that “there is anarchy in the country” and asserted: “We don’t want anarchy in the country.”

[…]

The hearing

[…].

Subsequently, the court ruled that Imran’s arrest was “illegal” and directed the PTI chief to approach the IHC. “You will have to accept the high court’s decision,” the top judge said, reiterating that Imran had to appear before IHC tomorrow (Friday).

Justice Mazhar said that the SC would direct the high court to fix a hearing for 11am tomorrow, while the CJP stated that Attorney General for Pakistan (AGP) Mansoor Usman Awan would be the guarantor for security.

[…]

“We don’t want you to be harmed,” Justice Bandial said. “Imran Khan will stay at the guest house as a guest [and] his protection would be the government’s responsibility,” he added.

“The case will resume from where the matters became complicated,” the top judge remarked, adding that a written order will be issued soon.

At the outset of the hearing — which commenced a little after 2pm — one of Imran’s counsels, Hamid Khan, came to the rostrum and informed the apex court that his client had approached the Islamabad High Court (IHC) for pre-arrest bail.

[…]

The CJP asked Imran’s counsel about the number of Rangers personnel who had carried out the arrest of the former premier. Imran’s lawyer responded that “100 rangers personnel entered court premises” in order to arrest the PTI chief.

“What dignity remains of the court if 90 people entered its premises? How can any individual be arrested from court premises?” he asked.

“In the past, action has been taken against lawyers for vandalism inside the court,” he observed. “If an individual has surrendered to the court, then what does arresting them mean?”

He further said that NAB had committed “contempt of court”. “They should have taken permission from the court’s registrar before the arrest. Court staffers were also subjected to abuse,” he added.

CJP Bandial emphasised that courts should be accessible to everyone for relief and that individuals should feel safe to approach the courts.

Imran’s lawyer then demanded that his client be released from NAB custody, stating that the arrest was made without an investigation officer present.

The chief justice noted that the court was currently examining the manner in which the arrest was conducted and whether contempt had taken place.

[…]

“No one can be arrested from the Supreme Court, a high court or an accountability court,” the CJP said.

Imran’s lawyer Hamid said that if that the party would not have approached the SC if the PTI chief had been arrested from outside his home or outside the court.

Here, Justice Mazhar asked if Imran had responded to the NAB notice, to which the lawyer replied in the affirmative.

“According to the law, an arrest cannot be made when an inquiry is still being carried out,” Hamid said.

[…]

But Justice Minallah said that NAB had “not learnt its lessons”. He observed that NAB had been accused of many things, including “political engineering”. “Had NAB taken permission from the registrar?” he asked, adding that a letter had been written to the interior ministry for the warrant’s execution.

[…]

Via https://www.dawn.com/news/1752306/sc-orders-immediate-release-of-imran-after-terming-arrest-unlawful

 

 

 

 

 

 

Gazprom Continues to Supply Gas to Europe via Ukraine


By ECD1/TCO1

Quite curious that a Russian company is able to continue supplying Europe through the country they are fighting and despite the alleged sanctions.

Weird how things work sometimes.

Gazprom continues to supply gas to Europe through Ukraine via the Soudja station. Yesterday it delivered 37 million cubic meters of gas, a Gazprom press release has stated.

“Gazprom transports Russian gas through Ukraine in the amount confirmed by the Ukrainian side through the Soudja station, i.e. 37 million cubic meters by April 29. The request for pumping through Sokhranovka was rejected,” he said.

The previous day’s transit volume was 42.4 million cubic meters.

Gas transportation through Ukraine remains the only route to Western and Central Europe. Pumping through the Nord Stream 1 pipeline has stopped completely. Turkish Stream and Blue Stream are destined for Turkey and countries in southern and southeastern Europe.

Russia announced on Friday that the Nord Stream 1 pipeline, which runs under the Baltic Sea to connect Russia with Germany and other Western European countries, would not restart on Saturday as planned due to an oil leak detected during maintenance operations over the past few days.

Usually the German group Siemens Energy carries out the maintenance of the Nord Stream 1 turbines, but this time it was not involved in the work carried out by Gazprom.

Via https://elcolectivodeuno.wordpress.com/2023/05/11/gazprom-continues-to-supply-gas-to-europe-via-ukraine/

Covid Jabs the Big Picture

Health Advisors and Recovery Team (HART)

Part 1

[…]

The regulators failed us in numerous ways as set out in The Perseus Report.  Examples include:

  1. Companies were allowed to skip testing for gene and cancer toxicity and even studies showing how much spike is produced, for how long and where in the body it reaches. Pfizer said these studies were “not considered necessary.” Even while their trial info sheet said “Due to the urgent need for a vaccine against Covid-19, with agreement from the MHRA, some of the tests usually required for a newly manufactured vaccine.have been modified, in order to make the vaccine available more quickly for assessment.”
  2. They did not demand these studies were done after rushed emergency approvals either. No human studies were carried out to see what happened to the synthetic modified RNA – no-one knows how long it takes to be removed from the body. There is evidence that in some it lasts between at least 28 days and 4 months in the blood.
  3. The regulators let the pharma companies get away with terminating the placebo arm of the study after ~3 months by offering them all the novel products. This was despite us knowing that narcolepsy caused by Pandemrix vaccine took on average of 8 months to be diagnosed.
  4. The lipid nanoparticles that deliver the modified synthetic mRNA are themselves toxic. This mechanism of delivery was shelved in 2016 for gene therapy to treat inherited genetic conditions because of the multiple doses needed. It was claimed it could still be used in vaccine technology because that only requires one dose…
  5. The viral vector used for delivering the AstraZeneca DNA message was reported in 2007 to cause platelet activation, which can lead to blood clots.
  6. There were many more points made including failings in investigating deaths, failing to listen to patients, problems with manufacturing processes and problems with accountability and governance all of which are in the report.

Since 2005 there have been concerns about the regulator losing “sight of the need to protect and promote public health.” The CEO of the MHRA, Dame June Raine, claims the MHRA is now an “enabler” not a “watchdog.” Even before there was political capture there were pre-existing conflicts of interest.

The spike protein is the most toxic part of the virus. It damages lungs, vessel walls and causes clots. Part of the sequence is identical to a region of a bacterial sequence that can bind directly to a particular type of white blood cells resulting in lethal cytokine storms. This part of the sequence was heavily mutated in the Omicron variant making it less lethal. However, even the most recent injections contained the original Chinese spike sequence with this dangerous sequence.

The manufacturers decided to use the WHOLE Chinese spike sequence rather than parts of it, or peptides, which have been shown to be safer for vaccine design. Some manufacturers modified the spike so that it could not bind to the receptor and enter a cell. This might have reduced some harm from receptor binding but not from the action of spike within cells. The spike was delivered into cells so spike was produced INSIDE the cells in the first place. AstraZeneca did not modify the sequence. From November 2020 it was clear that parts of AZ spike could be shed outside of cells.

The Pfizer and Moderna clinical trial data shows a higher rate of serious adverse reactions from the treatment group (12.5 per 10,000) than any reduction in serious events from covid (2.3 and 6.4 per 10,000 for Pfizer and Moderna respectively). Yet the claim of 90%+ efficacy was all that was reported and all that Dame June Raine claimed she needed to see in order to approve the drugs.

AZ issued a press release claiming 100% efficacy against hospitalisation and death after only two severe covid hospitalisations and one death in the placebo arm. This claim was repeated widely and was believed.

At the time, the priority was to protect the old and vulnerable who accounted for 98% of covid deaths. There were going to be 15 million jabs to freedom:

The evidence presented is damning. The failures of the regulators to adequately test the safety and efficacy of these novel vaccines are shocking. The circular belief that vaccines required fewer safety checks than other novel therapies is a dangerous assumption that has put the lives of millions at risk. The fact that serious adverse reactions were higher in the treatment group than any reduction in serious events from covid is deeply concerning. We must demand accountability from the regulators and demand that the safety and wellbeing of the public is always the top priority, not profit or political gain. There was total regulatory failure in allowing these products to be given to anyone, which was compounded by not withdrawing them promptly once evidence these issues were clinically relevant became clear.

Via https://www.hartgroup.org/jabs-part-1/

Does Vaccine-Induced Myocarditis Put Teens at Risk of Future Heart Attacks?

By  Peter A. McCullough, M.D., MPH

A new study shows that six months after being diagnosed with vaccine-induced myocarditis, 80% of teens had not recovered.

Every cardiology office in America should be recognizing COVID-19 vaccine-induced myocarditis presenting in young persons, 90% are male, with chest pain, effort intolerance, arrhythmias and cardiac arrest after injections of mRNA vaccines.

As I see these patients, the common question is, “When is this over?”

While electrocardiogram and blood tests tend to normalize quickly, my concern is that ongoing inflammation is occurring due to the continued production of the Wuhan spike protein coded by the long-lasting Pfizer or Moderna mRNA vaccines.

While blood tests can give inferences on inflammation, cardiologists also use cardiac MRA to visualize the inflammation, establish the diagnosis, and craft a prognosis.

We would hope young teenagers would resolve their MRI results and go on with life. A recent report to the contrary caught my attention.

Barmada et al studied a clinical cohort consisting of 23 patients hospitalized for vaccine-associated myocarditis and/or pericarditis. The cohort was predominately male (87%) with an average age of 16.9 ± 2.2 years (ranging from 13 to 21 years).

Patients had largely noncontributory past medical histories and were generally healthy before vaccination. Most patients had symptom onset 1 to 4 days after the second dose of the BNT162b2 mRNA vaccine.

Six patients either first experienced symptoms after a delay of >7 days after vaccination or were incidentally positive for SARS-CoV-2 by polymerase chain reaction (PCR) testing upon hospital admission; these six patients were thus excluded from further analyses, although they potentially reflect the breadth of clinical presentations of vaccine-associated myopericarditis.

The remaining cohort of 17 patients showed no evidence of recent prior SARS-CoV-2 infection, with antibodies to spike protein but not to nucleocapsid protein and negative nasopharyngeal swab reverse transcription quantitative PCR at hospital admission.

Credit: Anis Barmada et al.

While the authors clearly show high levels of inflammatory markers, my attention was drawn to the follow-up MRI scans.

As shown in the figure, only 20% had resolved their abnormalities (late gadolinium enhancement) at over six months (199 days).

This paper raises questions: 1) is there ongoing heart damage and inflammation at six months? 2) does the LGE in 80% represent a permanent “scar” putting these children at risk for future cardiac arrest?

These data strongly call for large-scale research into this emerging problem given the large number of potential young persons at risk.

[…]

Via https://childrenshealthdefense.org/defender/covid-vaccine-myocarditis-teen-heart-attack/

Lula to Propose Ukraine Peace Initiative at G7 Meeting

President Lula da Silva, Brasilia, Brazil, May 9, 2023.

President Lula da Silva, Brasilia, Brazil, May 9, 2023. | Photo: Twitter/ @JorgeGestoso

teleSUR Newsletter

The Brazilian president’s international affairs advisor Celso Amorim traveled to Ukraine and Russia to find out what the parties in conflict want.

On Tuesday, the Brazilian President Lula da Silva announced that he will invite India and Indonesia to join the club of countries he wants to form to mediate in favor of a negotiated solution to the Ukrainian conflict.

“It is the time for diplomacy, it is not the time for war,” he said in a joint statement with Dutch Prime Minister Mark Rutte made at the Planalto Palace in Brasilia.

“We need to find someone to discuss peace and Brazil is willing to do so,” said Lula, who will propose the creation of a group of mediating countries during the next meeting of the Group of Seven (G7) to be held in Japan from May 19 to 21.

“Peace is the first path. It is to stop the war and thus create conditions to negotiate an end,” the Brazilian president reiterated, explaining that the solution to the Ukrainian conflict must be a “compromise solution” that satisfies both parties.

Lula’s statements come at a time when his top adviser on international affairs, Celso Amorim, traveled to Ukraine to meet with President Volodimir Zelenski. Previously, Amorim had a meeting with Russian President Vladimir Putin.

“I hope Celso brings me a solution so that we can talk about peace. He knows what Putin wants and he will know what Zelenski wants. That way we will have instruments to talk with other countries and possibly stop this war,” the Brazilian president said.

Currently, Prime Minister Rutte is on a three-day visit to Brazil, where he will hold meetings in the cities of Sao Paulo, Brasilia and Fortaleza.

RFK Jr Calls for Study on SSRI/Mass Shootings Link

“Anecdotally, it appears that almost every one of these shooters were on SSRIs or some other psychiatric drug. And this is only happening in America where … we take four times as many [psychiatric drugs] as the average European country.” stated

@RobertKennedyJr. “Prior to the introduction of Prozac, those shootings just were almost unknown, and now they’re an everyday affair. But NIH will not study that because it will offend the pharmaceutical industry. And it’s something that we ought to be studying.”

Via https://talesfromtheconspiratum.blog/2023/05/10/robert-kennedyjr-shakes-up-big-pharma-with-the-inconvenient-truth-about-mass-shootings/

Arkansas National Guard Takes Over Multinational Training for Ukraine

>Authority over the Joint Multinational Training Group — Ukraine mission is transferred from Task Force Orion, 27th Infantry Brigade Combat Team, New York Army National Guard, to Task Force Bowie, 39th IBCT, Arkansas Army National Guard, during a ceremony in Grafenwoehr, Germany, April 28, 2023. JMTG-U ensures the combat effectiveness of Armed Forces of Ukraine soldiers training on systems and equipment issued under the U.S.’ Presidential Drawdown Authority, and training in combined arms and joint maneuver. (Spc. Christian Carrillo)

Joint Multinational Training Group – Ukraine. Photo: Spc. Christian Carrillo/US National Guard