VAERS data released Friday by the CDC included a total of 818,044 reports of adverse events from all age groups following COVID vaccines, including 17,128 deaths and 122,833 serious injuries between Dec. 14, 2020, and Oct. 15, 2021.

Data released Friday by the Centers for Disease Control and Prevention (CDC) showed that between Dec. 14, 2020, and Oct. 15, 2021, a total of 818,044 adverse events following COVID vaccines were reported to the Vaccine Adverse Event Reporting System (VAERS).

The data included a total of 17,128 reports of deaths — an increase of 362 over the previous week, and a new report of a 12-year-old who died after getting the Pfizer vaccine.

There were 117,399 reports of serious injuries, including deaths, during the same time period — up 5,434 compared with the previous week.

Excluding “foreign reports” to VAERS, 612,125 adverse events, including 7,848 deaths and 50,225 serious injuries, were reported in the U.S. between Dec. 14, 2020, and Oct. 15, 2021.

Of the 7,848 U.S. deaths reported as of Oct. 15, 11% occurred within 24 hours of vaccination, 15% occurred within 48 hours of vaccination and 28% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.

In the U.S., 406.1 million COVID vaccine doses had been administered as of Oct. 15. This includes: 237 million doses of Pfizer, 154 million doses of Moderna and 15 million doses of Johnson & Johnson (J&J).

The data come directly from reports submitted to VAERS, the primary government-funded system for reporting adverse vaccine reactions in the U.S.

Every Friday, VAERS makes public all vaccine injury reports received as of a specified date, usually about a week prior to the release date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.
Historically, VAERS has been shown to report only 1% of actual vaccine adverse events.

This week’s U.S. data for 12- to 17-year-olds show:

• 21,921 total adverse events, including 1,325 rated as serious and 25 reported deaths. Two of the 25 deaths were suicides.

The most recent death involves a 12-year-old girl (VAERS I.D. 1784945) who died from a respiratory tract hemorrhage 22 days after receiving her first dose of Pfizer’s vaccine.

Another recent death includes a 15-year-old male who died six days after receiving his first dose of Pfizer’s COVID vaccine. According to his VAERS report (VAERS I.D. 1764974), the previously healthy teen complained of brief unilateral shoulder pain five days after receiving his COVID vaccine.

The next day he played with two friends at a community pond, swung on a rope swing, flipped into the air, and landed in the water feet first. He surfaced, laughed and told his friends “Wow, that hurt!” He then swam toward shore underwater, as was his usual routine, but did not re-emerge.

An autopsy showed no external indication of a head injury, but there was a small subgaleal hemorrhage — a rare, but lethal bleeding disorder — over the left occiput. In addition, the boy had a mildly elevated cardiac mass, increased left ventricular wall thickness and small foci of myocardial inflammation of the lateral wall of the left ventricle with myocyte necrosis consistent with myocardial infarction.

• 57 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death — with 96% of cases attributed to Pfizer’s vaccine.
• 535 reports of myocarditis and pericarditis (heart inflammation) with 527 casesattributed to Pfizer’s vaccine.
• 119 reports of blood-clotting disorders, with all cases attributed to Pfizer.

This week’s U.S. VAERS data, from Dec. 14, 2020, to Oct. 15, 2021, for all age groups combined, show:

• 19% of deaths were related to cardiac disorders.
• 54% of those who died were male, 42% were female and the remaining death reports did not include gender of the deceased.
• The average age of death was 72.7.
• Of the 3,014 cases of Bell’s Palsy reported, 51% were attributed to Pfizer vaccinations, 41% to Moderna and 8% to J&J.
• 666 reports of Guillain-Barré syndrome, with 40% of cases attributed to Pfizer, 31% to Moderna and 28% to J&J.
• 2,010 reports of anaphylaxis where the reaction was life-threatening, required treatment or resulted in death.
• 10,290 reports of blood clotting disorders. Of those, 4,488 reports were attributed to Pfizer, 3,709 reports to Moderna and 2,040 reports to J&J.
• 2,878 cases of myocarditis and pericarditis with 1,815 cases attributed to Pfizer, 939 cases to Moderna and 114 cases to J&J’s COVID vaccine.

Michigan woman died from blood clots after J&J vaccine, autopsy confirms 

A 60-year-old woman died from blood clotsafter receiving J&J’s COVID vaccine, according to an autopsy report released Sept. 20 by Dr. Michael Caplan, a forensic pathologist at Michigan Medicine.

Story at-a-glance:

• Lab-grown meat offers private corporations the opportunity to place intellectual property rights on meat development and thus create a financial windfall.
• Corporations that control the food supply through central production and distribution can also control populations and countries.
• Lab-grown meat originates from stem cells harvested from muscle tissue and multiplied in the lab — but the ability to culture tissue cells does not mean the product has health benefits for the end-user.
• Scientists are now working on lab-grown meat made from human cells that are being harvested from the inside of your cheek. While some argue over whether this is cannibalism, another question must be asked about how this will impact the spread of disease.

July 12, 2018, the U.S. Food and Drug Administration (FDA) convened a public meeting to talk about what to call lab-grown meat. As reported in The Atlantic, at the end of the meeting there was no consensus. The war of words was aimed at choosing an association that would evoke a specific emotional response in the consumer.

Various speakers got up and called the lab growth “clean meat,” “artificial meat,” “in vitro meat,” “cell culture products,” “cultured meat” or “culture tissue.” Each term had its advocates and critics.

For example, the beef producers didn’t like the term “clean meat.” Danielle Beck, a lobbyist for the National Cattlemen’s Beef Association told the reporter from The Atlantic the term is “inherently offensive to traditional meat producers, as if real meat is somehow dirty.”

However, that’s exactly what the fake meat industry would like you to believe. In fact, the lab-grown meat market rests on the shoulders of the claim that eating real meat is destroying our planet. Singapore was the first country to give regulatory approval for products that look like meat and did not come from real animals.

The decision paved the way for the rest of the world, and today fake meat is becoming so popular that you’ll find it in most Walmarts, Targets, other grocery stores and some popular chain restaurants. The fake meat industry offered their product as a light in a dark world, as many were laboring under the excessive news reports of COVID-19 cases.

It may have seemed that the big tech giantswere looking out for the food supply at an unprecedented time in history. But you don’t have to look too deeply into what’s happening to discover that patented fake meat is not about “saving the planet” or “sustainability” but, instead, is just another foray into controlling populations and amassing great wealth.

Lab-Grown meat is about Big Business

The food critic for the Financial Times wrote a piece in early September 2021, in which he made a strong case for how lab-grown meat is not about sustainability or making “green” decisions but, rather about intellectual property (IP) and creating a financial windfall.

He took a historical perspective on IP, listing the patents that have been filed protecting breakfast cereals, carbonated beverages, drugs, vaccines, genetically modified plants and pesticides. In each case the IP owned by Kellogg, Coca-Cola, McDonald’s, Big Pharmaand agrichemical businesses was the lifeblood of their financial success. He writes:

“Currently, there’s not a lot of IP in the meat industry … Saving animal lives, preventing the clear-cutting of rainforest, even the reduction of methane farts don’t excite investors — those changes can’t translate to profit.

“The holy grail is replacing the meat we consume with a proprietary product, owning the IP on meat. Coca-Cola and McDonald’s managed to grow patented food products into two of the top food companies on the globe by market cap, but a patent on animal-free ‘meat’ could entirely dwarf their achievements.”

Bill Gates promotes the idea of eating 100% synthetic beef to fight climate change.
The idea is one of his core tenets in his new book in which he lays out how to eliminate greenhouse gas emissions. Mind you, this book was written by a man who built a 65,993 square-foot (6,131 square-meter) home with a 23-car garage, 20-person cinema and 24 bathrooms. He owns five other homes, a horse farm, four private jets and a “collection” of helicopters.

According to one study reported in Business Today, his annual carbon footprint is 7,493 metric tons of carbon, much of which is produced by his aircraft. In an article published in Forbes, March 22, one reporter writes:

“Now, I don’t necessarily agree with Gates. And I hate the idea of governments deciding what their citizens should eat (which seems to be what Gates is suggesting). But my job is to help you make money. And there’s no question that there’s billions to be made in the technology behind plant-based meat.”

Unfortunately, that may be the path that many will take to acquire wealth over health. Beyond Meat is already worth $12 billion10 and it’s projected to double by 2025. And yet, as the Forbes reporter points out, the meat industry is the tip of the iceberg.

Synthetic biology uses technology to allow scientists to program life. It reconfigures DNA so that it produces something entirely new.

This is the technology that Beyond Meat uses to create more “realistic” burgers using soybeans. He also points out that Moderna and Pfizer COVID vaccines are made of a synthetic strand of genetic code and goes on to write, “I believe, with the possible exception of artificial intelligence (AI), synthetic biology has the biggest potential of any disruptive technology to radically reshape our world.”

Control food supply = Control populations and countries

In January 2021, an analysis by The Land Report found that Bill Gates owns 242,000 acres of farmland in the U.S. This has made him the largest private farmland owner. During Gates’ interview with MIT Technology Review, Gates said:

“So no, I don’t think the poorest 80 countries will be eating synthetic meat. I do think all rich countries should move to 100% synthetic beef. You can get used to the taste difference, and the claim is they’re going to make it taste even better over time. Eventually, that green premium is modest enough that you can sort of change the [behavior of] people or use regulation to totally shift the demand.”

It is the last sentence in that paragraph that makes the most sense as you consider how Gates and other technocrats are aiming at controlling populations through central production and distribution of food. He says, “change the behavior of people or use regulation to totally shift the demand.” Promoting lab-grown protein is not about sustainability but, rather, about wealth and power.

Using intellectual property, tech giants hope to replace living animals with patented plant- and animal-derived alternatives, which will effectively control food supply. And Gates’ 242,000 acres of farmland spread across Illinois, Louisiana, California, Iowa and nearly one dozen other states appear to be earmarked for genetically engineered corn and soy crops. In other words, he’s farming the basic crops needed for (plant-based) fake meat and processed foods.

Lab-grown meat alternatives differ from their vegetarian counterparts by virtue of initially starting with cell cultures from living animals. Mosa Meat grows their meat after harvesting a small number of cells from livestock “who are then returned, almost unscathed, to their fields.”

As described in Popular Mechanics, Memphis Meats, in which Gates is a serious investor, tries to avoid animals whenever possible. Instead, they use cells that have been procured from animal biopsies.

In other words, when a veterinarian has decided to biopsy an area of an animal to make a medical determination about an abnormal growth, Memphis Meats harvests cells that would have otherwise been discarded and grows those into lab grown meat. Swapping traditional, whole food grown by small farmers for mass-produced fake foods is part of the plan for The Great Reset.

The objective is to control the entire food supply. To that end, researchers and manufacturers are also looking at milk proteins made from genetically engineered Trichoderma reesei fungus to produce a dairy-like protein casein and whey. Popular Science named Perfect Day’s animal-free whey protein as the Grand Award winner in the engineering category of the 100 greatest innovations of 2020.

The EAT Forum, co-founded by the Wellcome Trust, developed a Planetary Health Dietdesigned to be applied to the global population. It entails cutting meat and dairy intake by up to 90% and replacing it largely with foods made in laboratories, along with cereals and oil.

Their largest initiative is called FReSH, which aims to transform the food system by working with biotech and fake meat companies to replace whole foods with lab-created alternatives. In other words, once tech giants have control of meat, dairy, cereals and oils, they will be the ones profiting from and controlling the food supply.

Private companies that control the food supply will ultimately control countries and entire populations. Biotech will eventually push farmers and ranchers out of the equation and will threaten food security. In other words, the work being done in the name of sustainability and saving the planet will give greater control to private corporations.

Health dangers associated with linoleic acid

It’s important to realize that whether it is plant-based or lab-grown, fake meat is a processed food. Imitation meat is not better, or even equal, to real meat. Foods that are not directly from the ground, vines, bushes, trees, bodies of water or animals are considered processed.

Lab-grown meat starts with a muscle sample from a cow. Once in the lab, technicians separate stem cells from the sample and then multiply those dramatically. The cells differentiate into fibers that form muscle tissue. Mosa Meat believes that one tissue sample can yield 80,000 quarter-pounders.

Tissue growth inside an animal occurs when the blood supply delivers appropriate nutrients to produce healthy muscle growth. This requires that the animal is fed a whole and balanced diet, from which the body extracts the necessary nutrients in an appropriate amount to feed the cells.

The human body then extracts the nutrients found in regeneratively and biodynamically pastured meat. However, as science has demonstrated in the last two decades, growing cells on sugar causes growth, but will not yield health. The sheer ability to grow lab-cultured meat does not indicate that the end product will have any health benefit to the end-user.

Plant-based fake meat contains excess amounts of omega-6 fat in the form of linoleic acid (LA). This is one of the most significant contributors to metabolic dysfunction.

In my opinion, this metabolic poison is the primary contributor to the rising rates of chronic disease. LA leads to severe mitochondrial dysfunction, decreased NAD+ levels, obesity, insulin resistance and a radical decrease in the ability to generate energy.

The genetic engineering used to produce the flavor and texture of real meat does not reproduce healthy fatty acid composition because the substrate is canola and sunfloweroils as the primary sources of fat.

The sunflower oil used in both Impossible Burgers and Beyond Meats is 68% LA, which is an extraordinarily high amount.

It is dangerous because LA is susceptible to oxidation and causes oxidation byproducts called OXLAMs (oxidative linoleic acid metabolites). These byproducts devastate your DNA, protein, mitochondria and cellular membranes. This means that fake meat is failing all measures of sustainability and health.

Have you considered cultured meat from human cells?

While lab-grown meat and dairy products may sound like science fiction, the next step for food manufacturers comes directly out of the 1973 dystopian film “Soylent Green.” The science-fiction movie takes place in New York in 2022. In the story, the Earth is severely overpopulated, and people are living in the streets.

For sustenance, people are given rations of water and Soylent Green, which supposedly is a high-protein food made from plankton. In the end, you discover in this futuristic nightmare fantasy of controlling big corporations, that the high-protein drink is actually made by people.

Now, just months away from 2022, scientists are working on lab-grown “meat” made from human cells that are harvested from the inside of human cheeks. This grisly product was first presented as ‘art’ by a scientist and founder of the biotech firm Spiderwort. Tech Times reported Nov. 22, 2020, that:

“A new ‘DIY meal kit’ that can be used to grow steaks that are made mostly from human cells was just recently nominated by the London-based Design Museum as the ‘design of the year.’

“Called ‘Ouroboros Steak,’ this is named right after the circular symbol of a snake known for eating itself tail-first. This hypothetical kit would later on come with everything that one person would need in order to use their own cells to grow miniature human meat steaks …”

These kits are not commercially available — yet. But it begs the question of what possesses someone to think that eating a lump of meat made from your own body could be a viable idea? The question must also be raised about whether this is cannibalism.

Those defending the concept claim that since you’re eating your own body, it’s not cannibalism. However, if it ever becomes commercially available, what’s to prevent someone from growing meat from other people’s cells — and selling it?

And the ick factor aside, how could this impact the spread of disease? For example, tribal cannibalism in Papua, New Guinea, led to a prion disease, which nearly wiped out a tribe of people.

In many villages, after an individual died, the villagers would cook and consume the body in an act of grief. Scientists who studied the tribe believe that one person developed a sporadic incident of Crutchfield-Jakob disease, also known as mad cow disease. Eating the neurological tissue then spread the disease throughout the tribe.

It doesn’t take much to imagine that the strange and unusual side effects being reported by people after receiving a COVID-19 injection may have long-term effects on body tissue. What happens when you culture and eat that body tissue, from yourself or someone else?

source:the defender children health defense news and views By 

LONDON — What a difference three months can make.

On July 19, Britons celebrated as England marked "Freedom Day," seeing a near-full lifting of Covid-19restrictions. Covid-related hospitalizations and deaths were relatively low, even if cases continued to rise, and the country's vaccination rollout was largely lauded as a success internationally.

On the first episode of CHD.TV’s “The Jerusalem Report,” host Ilana Rachel Daniel gave an overview of life in Israel over the past 10 months with news and commentary on vaccine mandates, propaganda, censorship and Pfizer’s dirty deal with the government.

On the premier episode of CHD.TV’s “The Jerusalem Report,” host Ilana Rachel Danielexplained how her country led the world in time spent in coronavirus lockdowns, describing in detail what it’s been like this past year.

Daniel described how the people of Israel responded to the back-door deal between Pfizer and the Health Ministry that traded a discount on COVID vaccines in exchange for Israeli citizens’ private health and personal data, making Israel the first country to become a massive vaccine experiment.

Daniel said policy decisions were made absent of informed consent, were steeped in coercion and dishonest in intent.

“We are and were the lab rats of the world,” Daniel said. “To date, Israeli citizens have only ever seen a media-released, heavily redacted version of that contract,” between Pfizer and the Israeli government.

Daniel said:

“We’ve heard rumors of an alleged penalty clause if quotas are not reached. We’ve also heard Israeli vaccine developers being pushed out of the running by the government. It would appear we are beholden to Pfizer to the suppression of other treatments.”

She described outdoor mask mandates, citizens on house arrest and vaccine mandates, as well as Isreali passengers being removed from international flights.

“In a final blow to our claims of democracy,” Daniel said, “we are kept from disclosure of Corona [virus] Cabinet and similar session meeting minutes, as they have been put under a 30-year confidentiality act.”

Daniel quoted the State of Israel as saying, “The public’s right to know isn’t absolute.”

Also in this episode:

• Government-issued tracking devices on travelers to impose quarantine.
• The refusal of Israel to release COVID fatality data, despite all citizen’s medical records being property of the government.
• Israeli doctors are not admitting to vaccine injury. Daniel said trust in the medical establishment is waning among citizens.
• Citizens are afraid to speak out on vaccine injuries and deaths.
• Media propaganda campaigns for COVID vaccines targeted children and pregnant women and hid vaccine injury from citizens.
• Updates on Green Pass, boosters and censorship.

Daniel said the truth will come out. She said The Isreaeli People’s Committee, an independent investigative group reporting adverse events in Israel, and The Testimonies Project are documenting the truth of vaccine injury, government coercion and totalitarian-like conditions in Israel.

“It is clear to many here in Israel and abroad that we fight not only for ourselves, but intentionally for you as well,” Daniel said, reminding viewers that the citizens of Israel are watching the rest of the world fight for medical freedom.

She said, “Your wins, wherever they are found, are ours.”

“The Jerusalem Report” is hosted by Ilana Rachel Daniel. Each week Daniel invites listeners to hear the story of an unprecedented COVID response, a mass human experiment thrust upon the entire nation of Israel. Daniel is a health advisor, health and safety researcher, activist and writer.

source: the defender children health defense news and views 

Vaccine skeptics, vaccine refusers, vaccine deniers—these anti-vaxxers are scourges whose ignorance and misinformation are responsible for countless COVID-19 deaths, our public health authorities attest. Stamping their message out is so important that those with the biggest megaphones are being outed, threatened, and fired from their academic and medical posts, and wherever else they might be found.

So, who are these health heretics whose dangerous rhetoric is questioning prestigious public bodies such as the World Health Organization and the Centers for Disease Control and Prevention, blue-chip pharma companies such as Pfizer and Johnson & Johnson, and the great majority of governments?

Dr. Peter McCullough, the author of more than 1,000 publications with over 500 citations in the National Library of Medicine, is one of the most outspoken critics of government COVID policies. He testified to the Texas Senate HHS Committee that his treatment protocol, including hydroxychloroquine and ivermectin, led to an 85 percent reduction in mortality. He also has been critical of mass COVID-19 vaccination, in part given safety concerns about the vaccines.

“Today, we have 800 cases of young people developing myocarditis, or inflammation of the heart,” McCullough, a cardiologist and internal medicine physician, said in a webinar in June. “I’m going to opine that because there is no clinical benefit whatsoever in young people to get the vaccine that even one case is too many.”

Dr. Byram W. Bridle, an award-winning associate professor of viral immunology at the University of Guelph’s Department of Pathobiology, headed an advanced lab whose vaccine platform was funded by the Ontario government to develop a COVID-19 vaccine.

Dr. Robert Malone, the inventor of mRNA vaccines while at the Salk Institute in 1988, is also an inventor of DNA vaccines. He has some 100 peer-reviewed publications and published abstracts and 11,477 citations of his peer-reviewed publications. Malone believesthat for “high-risk populations, the risk/benefit ratio for the USA vaccines seem to make sense,” but that it’s “demonstrably false” to claim that “these genetic vaccines are the only path available to herd immunity” or are “perfectly safe.”

Malone, who is now allegedly subject to death threats, has become one of the most vilified scientists on earth, his accomplishments denigrated in magazines such as The Atlanticand throughout the mainstream and social media.

Others who have been vilified in the mainstream and social media include Dr. Jay Bhattacharya, professor at Stanford University Medical School, who stated that COVID-19 vaccination should be a matter of personal health and that “there’s no public health reason for a mandate“; Dr. Sunetra Gupta, infectious disease epidemiologist and professor of theoretical epidemiology at the University of Oxford, who stated that “it is really not logical to use vaccines to protect other people. … The bottom line is that these vaccines do not prevent transmission”; and Dr. Martin Kulldorff, professor of medicine at Harvard Medical School, who stated that“thinking that everyone must be vaccinated is as scientifically flawed as thinking nobody should. COVID vaccines are important for older high-risk people, and their care-takers. Those with prior natural infection do not need it. Nor children.”

Many more eminent COVID-19 vaccine skeptics have remained silent, for fear of being punished. In the United States, the Federation of State Medical Boards warned that “physicians who generate and spread COVID-19 vaccine misinformation or disinformation are risking disciplinary action by state medical boards, including the suspension or revocation of their medical license,” a warning repeated in Canada by provincial licensing bodies such as the College of Physicians and Surgeons of Ontario.

The ranks of the so-called vaccine skeptics include a Who’s Who of the world’s leading scientists. Few in the public know of them because they’ve been silenced, censored, and sidelined. Public health authorities may brand them as unscientific COVID kooks, but McCullough, Bridle, Malone, et al. haven’t been the ones acting as snake oil salesmen, offering instant cures to anyone in the crowd willing to chance their medicine.

The hard sell and sweeping claims have been coming from the public health officials, most of whom have far fewer scientific accomplishments, and are far less knowledgeable, than the vaccine skeptics they cavalierly dismiss.

source: the epoch times by Patricia Adams and Lawrence Solomon

A Michigan pathologist confirmed 60-year-old Sandra Jacobs died from cerebral venous sinus thrombosis, a rare blood-clotting disorder, after receiving Johnson & Johnson’s COVID vaccine.

A 60-year-old woman died from blood clotsafter receiving Johnson & Johnson’s (J&J) COVID vaccine, according to an autopsy report released Sept. 20 by Dr. Michael Caplan, a forensic pathologist for Michigan Medicine.

Sandra Jacobs “appears to have succumbed” to a “rare but nevertheless documented” complication associated with the viral vector vaccine — cerebral venous sinus thrombosis(CVST) — Caplan wrote in the summary.

According to Johns Hopkins Medicine, CVST occurs when a “blood clot forms in the brain’s venous sinuses,” preventing blood from draining out of the brain. “As a result, blood cells may break and leak blood into the brain tissues, forming a hemorrhage.”

This condition brought about “hemorrhagic cerebral infarct,” or stroke caused by brain bleeding, and brain swelling, Caplan wrote.

The death certificate, obtained after some difficulty by Jacobs’ daughter, Tatum Strieter-Byron, lists the cause of death as “complications of cerebral venous sinus thrombosis” and “recent administration” of a COVID vaccine as the contributing condition.

Caplan deemed the manner of death “natural.” It may also be considered a “therapeutic complication” since this is a known vaccine issue, he wrote. Under “final diagnosis,” Caplan first listed the COVID vaccine.

Jacobs died 13 days after receiving the single-dose J&J vaccine at a CVS pharmacy on April 8 — just five days before federal health agencies temporarily paused the vaccine while they examined an unusual blood-clotting disorder, Michigan Live reported.

Though it took months to confirm it, Strieter-Byron knew from the start her mother died from the vaccine.

“She was a real person. She is not a piece of, just like fictitious political propaganda, where they’re saying it doesn’t exist,” Strieter-Byron said. “It’s not true. It does exist. She was a real person with a real life.”

Michigan Live reached out to Caplan for comment, but efforts were unsuccessful. “In conjunction with the Washtenaw County Health Department, we have decided not to have Dr. Caplan or the medical examiner’s office provide comment on the case,” Dr. Allecia Wilson, the county’s chief medical examiner, wrote in an email.

J&J also did not respond to a request for comment. A doctor with the manufacturer’s COVID vaccine safety team called a reporter, but only to obtain Strieter-Byron’s information, who as of Oct. 15 had not heard from the doctor.

On April 13, federal agencies paused J&J’s COVID vaccine, marketed under its Janssen subsidiary, while they investigated the vaccine’s possible link to potentially dangerous blood clots.

During the April 23 meeting, the Centers for Disease Control and Prevention’s (CDC) Advisory Committee on Immunization Practices (ACIP) said it had identified 15 women diagnosed with rare blood clots, including three who died. Only two of the women were older than 50, with the risk highest in women ages 30 to 39.

The ACIP said the link between blood clots and J&J’s COVID vaccine was “plausible,” but concluded the vaccine’s “benefits outweighed the risks” and recommended the vaccine for persons 18 and older in the U.S. under the U.S. Food and Drug Administration’s (FDA) Emergency Use Authorization (EUA).

On April 26, the FDA amended its EUA for the J&J vaccine to reflect the risk of rare blood clots and said vaccinations could resume immediately.

According to the most recent data from the CDC’s Vaccine Adverse Event Reporting System (VAERS), between Dec. 14, 2020 and Oct. 8, 2021, there were 22,896 reports of blood clotting disorders. Of those, 15,190 reportswere attributed to Pfizer, 5,092 reports to Moderna and 2,551 reports to J&J.

Excluding foreign reports — those reports submitted to VAERS from outside the U.S. — there have been 10,131 reports of blood clotting disorders. Of those, 4,407 reportswere attributed to Pfizer, 3,654 reports to Moderna and 2,018 reports to J&J.

​​The Defender has reported on numerous cases of blood clots following COVID vaccination:

• Jessica Berg Wilson, a 37-year-old mother who died from vaccine-induced thrombotic thrombocytopenia after she received J&J’s COVID vaccine as a condition of volunteering at her child’s school.
• Emma Burkey, an 18-year-old teen was put on a respirator and underwent three brain surgeries from blood clots after receiving J&J’s vaccine.
• Anne VanGeest, a healthy 35-year-old, died of a brain hemorrhage 11 days after receiving J&J’s COVID vaccine.
• Brad Malagarie, 43, suffered a stroke from blood clots hours after receiving J&J’s COVID vaccine. The stroke left him unable to walk, talk and with paralysis on the left side of his body.
• Everest Romney, 17, developed blood clots after his first dose of Pfizer’s vaccine.

J&J’s vaccine has also been linked to Guillain–Barré syndrome (GBS), a “serious but rare” neurological disorder in which the body’s immune system mistakenly attacks part of its peripheral nervous system — the network of nerves located outside of the brain and spinal cord. GBS can range from a very mild case with brief weakness, to paralysis, which can leave the person unable to breathe independently.

The FDA concluded the benefits of the vaccine outweigh any danger but added a warning in fact sheets about the drug for providers and patients.

Children’s Health Defense asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.

source: the defender children health defense news and views 

The White House today unveiled plans to vaccinate 28 million 5- to 11-year olds for COVID, and the Centers for Disease Control and Prevention has already issued guidance for the vaccines for that age group, even though the U.S. Food and Drug Administration has yet to approve Pfizer’s vaccine for young children.

The White House today unveiled plans to roll out COVID vaccines for children ages 5 to 11, even though vaccine safety experts — who advise U.S. drug regulators and review safety and efficacy data — have not met to discuss whether Pfizer’s COVID vaccine should be authorized for use in the pediatric age group.

The Biden administration said it will secure enough vaccine doses to vaccinate the 28 million children ages 5 to 11 who would become eligible if the vaccine is authorized for that age group, CNN reported.

The White House will also help equip more than 25,000 pediatric and primary care offices, hundreds of community health centers and rural health clinics as well as tens of thousands of pharmacies to administer the shot.

Jeff Zients, White House COVID-19 response director, said 15 million doses will be ready to ship within a week after the vaccine is authorized, with millions of additional shots coming each week thereafter.

“We know millions of parents have been waiting for [a] COVID-19 vaccine for kids in this age group,” Zients told reporters during a COVID briefing. “And should the FDA and (U.S. Centers for Disease Control and Prevention) authorize the vaccine, we will be ready to get shots in arms.”

Zients said kids have different needs than adults and “our operational planning is geared to meet those specific needs, including by offering vaccinations in settings that parents and kids are familiar with and trust.”

The administration said it is launching a partnership with the Children’s Hospital Association “to work with over 100 children’s hospital systems across the country to set up vaccination sites in November and through the end of the calendar year.”

The administration plans to make vaccination available at school and other “community-based sites” with help from Federal Emergency Management Agency funding.

The U.S. Department of Health and Human Services (HHS) will also carry out a national public education campaign “to reach parents and guardians with accurate and culturally responsive information about the vaccine and the risks that COVID-19 poses to children.”

As has been the case for adult vaccinations, the administration believes trusted messengers — educators, doctors and community leaders — will be vital to encouraging vaccinations, according to U.S. News & World Report.

The White House began laying the groundworkwith states earlier this month, asking governors to enroll pediatricians and other providers in vaccination programs so they could start administering shots as soon as they were ready.

“In the era of Delta, children get infected as readily as adults do, and they transmit the infection as readily as the adults do,” Dr. Anthony Fauci, White House chief medical advisor, told reporters Wednesday. “We may not appreciate that, because about 50% of the infections in children are asymptomatic.”

According to the American Academy of Pediatrics, less than 2% of children known to be infected by the coronavirus are hospitalized, and less than 0.03% of those infected die.

As The Defender reported in June, experts testifying before the FDA, when it was considering authorizing Pfizer’s vaccine for 12- to 15-year-olds, argued the risks did not outweigh the benefits, even for that older age group.

Vaccinating children for the benefit of adults is an “unproven hypothetical benefit,” Peter Doshi, Ph.D., associate professor University of Maryland School of Pharmacy and senior editor of The BMJ, told the FDA.

Doshi reminded FDA officials they cannot authorize or approve a medical product in a population unless the benefits outweigh the risks in that same population.

“If the FDA does not have a high bar for EUAs [Emergency Use Authorization] and licensing, the point of regulation is lost,” Doshi said.

Vaccine advisers to the FDA aren’t scheduled to meet until Oct. 26 to consider Pfizer’s request to authorize its vaccine for children ages 5 to 11. In the meeting, the advisers will review the company’s data and FDA’s own assessment, then vote on whether the FDA should grant EUA.

The CDC will convene its committee of independent vaccine experts on Nov. 2 and 3 to set official recommendations for the vaccine’s use.

If authorized, this would be the first COVID vaccine for younger children. The Pfizer-BioNTech vaccine is currently approved for people age 16 and older and has emergency authorization for children ages 12 to 15.

CDC issues guidance on administering Pfizer-BioNTech vaccine to kids ahead of meeting

The White House isn’t alone in making plans to vaccinate 5- to 11-year-olds official in advance of the vaccine being authorized for that age group. The CDC last week issued guidanceoutlining key aspects of a COVID vaccination program for children younger than 12 years old “designed to inform jurisdictional planningunder the assumption of FDA authorization and CDC recommendations of at least one COVID-19 vaccine product for children of this age.”

The CDC’s “Pediatric COVID-19 Vaccination Operational Planning Guide” includes details about the anticipated Pfizer-BioNTech vaccine— though it may be updated as other manufacturers submit applications for FDA review — and is based on “current facts and planning assumptions.”

In the document, the CDC lays out the differences between the pediatric vaccine and adult vaccine, gives detailed product configuration and provides a distribution strategy.

In addition, the CDC informed providers the Public Readiness and Emergency Preparedness (PREP) Act and PREP Act Declaration issued by the HHS Secretary “authorize and provide liability protections to licensed providers and others identified in the declaration to administer COVID-19 vaccines authorized by FDA, including COVID-19 vaccines authorized for administration to children.”

Beginning Oct. 20, states and other jurisdictions will be able to preorder doses of the Pfizer-BioNTech COVID vaccine formulated for children ages 5 to 11, according to the CDC’s federal planning document. The orders are in anticipation of a rollout that could begin as early as Nov. 3.

The CDC said jurisdictions should be ready to vaccinate children 5–11 years old shortly thereafter pending FDA authorization and CDC recommendation.

“By the White House already purchasing 65 million pediatric doses of the Pfizer-BioNTech vaccine, and the CDC putting out guidelines ahead of FDA authorization — let alone, a recommendation by its own Advisory Committee on Immunization Practices — these actors are revealing the whole vaccine regulatory process to be a complete sham,” said Mary Holland, president of Children’s Health Defense in an email to The Defender.

“There could be no better way to undermine public confidence than to make it clear that this is politics, not science.”

source: the defender children health defense news and views by Megan Redshaw 

Pfizer has used its position as a producer of one of the leading COVID-19 vaccines to “silence governments, throttle supply, shift risk, and maximize profits” through secret contracts with countries around the world, according to a Public Citizen report published Tuesday.

“Behind closed doors, Pfizer wields its power to extract a series of concerning concessions from governments,” report author Zain Rizvi, law and policy researcher at Public Citizen’s Access to Medicines program, said in a statement. “The global community cannot allow pharmaceutical corporations to keep calling the shots.”

The new report begins by noting February reporting about accusations of Pfizer — an American pharmaceutical giant that developed its mRNA vaccine with the German firm BioNTech — “bullying” Latin American governments during contract negotiations for doses.

Public Citizen obtained unredacted term sheets, drafts or final agreements between Pfizer and Albania, Brazil, Colombia, the Dominican Republic, the European Commission and Peru. The consumer rights advocacy group also examined redacted contracts with Chile, the U.S., and the U.K.

Based on those contracts, the report identifies six tactics Pfizer is using to serve the company rather than public health in the midst of a deadly pandemic:

1. Pfizer reserves the right to silence governments

The Brazilian government complained earlier this year that the company insisted on “unfair and abusive” terms but ultimately accepted a contract that “waived sovereign immunity; imposed no penalties on Pfizer for late deliveries; agreed to resolve disputes under a secret private arbitration under the laws of New York; and broadly indemnified Pfizer for civil claims.”

Brazil also agreed to a nondisclosure provision similar to those found in contracts with the European Commission and the U.S. government.

2. Pfizer controls donations

Again using Brazil as an example, the report points out that the South American nation must first get a go-ahead from Pfizer to accept donations or buy its vaccines from others. The country is also barred from “donating, distributing, exporting, or otherwise transporting the vaccine outside Brazil without Pfizer’s permission.”

3. Pfizer secured an “IP waiver” for itself

Pfizer CEO Albert Bourla “has emerged as a strident defender of intellectual property in the pandemic,” the report says, noting his opposition to a proposal that members of the World Trade Organization who signed on to the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS) waive IP protections for COVID-19 vaccines and treatments during the crisis.

“But, in several contracts, Pfizer seems to recognize the risk posed by intellectual property to vaccine development, manufacturing, and sale,” Public Citizen explains. “The contracts shift responsibility for any intellectual property infringement that Pfizer might commit to the government purchasers. As a result, under the contract, Pfizer can use anyone’s intellectual property it pleases — largely without consequence.”

4. Private arbitrators, not public courts, decide disputes in secret

While the U.K. contract requires that disputes are settled by secret panel of three private arbitrators under the Rules of Arbitration of the International Chamber of Commerce, the report says, “the Albania draft contract and Brazil, Chile, Colombia, Dominican Republic, and Peru agreements require the governments to go further, with contractual disputes subject to ICC arbitration applying New York law.”

5. Pfizer can go after state assets

“Pfizer required Brazil, Chile, Colombia, the Dominican Republic, and Peru to waive sovereign immunity,” the report highlights, detailing that the doctrine can sometimes protect states from companies trying to enforce decisions reached by the previously noted secret arbitral panels. Some of the contracts enable the company to “request that courts use state assets as a guarantee that Pfizer will be paid an arbitral award and/or use the assets to compensate Pfizer if the government does not pay,” according to Public Citizen.

6. Pfizer calls the shots on key decisions

“What happens if there are vaccine supply shortages? In the Albania draft contract and the Brazil and Colombia agreement, Pfizer will decide adjustments to the delivery schedule based on principles the corporation will decide” the report notes, concluding that “under the vast majority of contracts, Pfizer’s interests come first.”

Public Citizen calls on world leaders, especially U.S. President Joe Biden, to “push back” against Pfizer’s negotiating tactics and “rein in” its monopoly power.

According to the group, the Biden administration can “call on Pfizer to renegotiate existing commitments and pursue a fairer approach in the future” as well as “further rectify the power imbalance by sharing the vaccine recipe, under the Defense Production Act, to allow multiple producers to expand vaccine supplies.”

The U.S. administration “can also work to rapidly secure a broad waiver of intellectual property rules,” the report adds, declaring that “a wartime response against the virus demands nothing less.”

In response to Public Citizen’s report, Sharon Castillo, a spokesperson for Pfizer, told The Washington Post that confidentiality clauses were “standard in commercial contracts” and “intended to help build trust between the parties, as well as protect the confidential commercial information exchanged during negotiations and included in final contracts.”

Castillo also said that “Pfizer has not interfered and has absolutely no intention of interfering with any country’s diplomatic, military, or culturally significant assets,” adding that “to suggest anything to the contrary is irresponsible and misleading.”

Meanwhile, Peter Maybarduk, director of Public Citizen’s Access to Medicines program, accused Pfizer of “taking advantage of countries’ desperation” with the far-reaching contracts.

“Most of us have sacrificed during the pandemic; staying distant to protect family and friends,” Maybarduk said Tuesday. “Pfizer went the other way, using its control of scarce vaccines to win special privileges, from people that have little choice.”

source: the defender children health defense news and views By 

Federal regulators will meet over the next two weeks to weigh the benefits of giving shots to kids, after lengthy studies meant to ensure the safety of the vaccines.

Within hours of formal approval, expected after the Centers for Disease Control and Prevention advisory meeting scheduled for Nov. 2-3, doses will begin shipping to providers across the country, along with smaller needles necessary for injecting young kids, and within days will be ready to go into the arms of kids on a wide scale.

The Biden administration notes the nationwide campaign to extend the protection of vaccination to the school-going cohort will not look like the start of the country’s vaccine rollout 10 months ago, when scarcity of doses and capacity issues meant a painstaking wait for many Americans. The country now has ample supplies of the Pfizer shot to vaccinate the roughly 28 million kids who will soon be eligible, White House officials said, and have been working for months to ensure widespread availability of shots once approved.

More than 25,000 pediatricians and primary care providers have already signed on to administer COVID-19 vaccine shots to kids, the White House said, in addition to the tens of thousands of retail pharmacies that are already administering shots to adults. Hundreds of school- and community-based clinics will also be funded and supported by the Federal Emergency Management Agency to help speed putting shots into arms.

The White House is also preparing to mobilize a stepped-up campaign to educate parents and kids about the safety of the shots and the ease of getting them. As has been the case for adult vaccinations, the administration believes trusted messengers — educators, doctors, and community leaders — will be vital to encouraging vaccinations.

While children are at lower risk than older people of having serious side effects from COVID-19, those serious consequences do occur – and officials note that vaccination both dramatically reduces those chances and will reduce the spread of the more transmissible delta variant in communities, contributing to the nation’s broader recovery from the pandemic.

The administration notes that kids who get their first shot within a couple weeks of the expected approval in early November will be fully vaccinated by Christmas.

The reports reveal that the board is still negotiating its relationship with the social network and says its own credibility depends on Facebook’s being more forthcoming.

Facebook’s Oversight Board issued a strong reprimand against the company in a set of quarterly reports Thursday, accusing it of not being “fully forthcoming” about a key program. The reports highlight the tense negotiations between the two entities, as the board tries to force greater transparency from the social media giant, despite its limited power.

GENEVA: Ten thousand Yemeni children have been killed after the Iran-aligned Houthi group ousted the government in 2015, the United Nations children’s agency UNICEF said on Tuesday.
“The Yemen conflict has just hit another shameful milestone. We now have 10,000 children who have been killed or maimed since ... March 2015,” UNICEF spokesperson James Elder told a UN briefing in Geneva after returning from a visit to Yemen.
“That is the equivalent of four children every single day,” Elder said, adding that many more child deaths or injuries went unreported.
Four out of every five children — a total of 11 million — need humanitarian assistance in Yemen, while 400,000 are suffering from acute malnutrition and more than 2 million are out of school, Elder said.
UN-led efforts to engineer a nationwide cease-fire have stalled as the Houthis resist compromise to end more than six years of a war that has caused what the UN calls the world’s largest humanitarian crisis.
Hundreds of Yemenis are trapped by fierce fighting between government and Houthi forces in the northern Marib governorate, residents and a local official said last week, after battles for control of the gas-rich region displaced some 10,000 people.

source: Arab news 

Morocco’s  Finance Bill 2022 is forecasted to grow at a rate of 3.2% and a budget deficit of 5.9% of Morocco’s GDP.

Morocco’s he Council of Government, chaired by the Head of Government Aziz Akhannouch, examined the finance bill on Monday.

The forecasts of the finance bill were presented during a press briefing by the government spokesperson, Mustapha Baitas; Nadia Fettah Alaoui, minister of economy; and Fouzi Lekjaa, minister delegate in charge of budget.

During the presentations, the officials predicted that the 2022 Finance Bill will result in the creation of 250,000 direct job opportunities in two years.

“The budget bill was prepared on the assumption of an estimated crop year of 80 million quitals and an average price of butane gas of $450 per tonne,” the spokesperson said.

The government council examined the draft finance bill for the year 2022 following a ministerial council meeting that was held in Fez on Sunday.

Alaoui's presentation to the King indicated that the bill will revolve around multiple axes.

The axes will prioritize the implementation of the new development model, which will seek to boost Morocco’s economy and improve the health sector.

Through the development model, Morocco seeks to initiate a universal social protection system.

The finance bill seeks to accelerate the generalization of preschool education for the purpose of strengthening the “basic knowledge” of children in primary schools.

The bill seeks to improve administrative work by accelerating the digitization of government services and administrative procedures. 

source: moroccoworldnews 

Royal Mansour has won many awards in recent years, and is widely considered to be the best in Morocco as well as among the finest worldwide.

The Royal Mansour in Marrakech has won the 2020-2021 Best Grand Hotel in the World Award.

Given by Prix Villegiature Awards, the prize gathers a voting jury composed of 22 international press correspondents and journalists from  highly reputed media outlets - such as Forbes Magazine, Financial Times, and Vogue - to reward the best hotels in Europe, Asia, Africa, and the Middle-East.

The Royal Mansour hotel comprises 53 individual riads, each with a courtyard, a living room, a bedroom, and a private rooftop terrace.

It also includes indoor and outdoor swimming pools, spas, and two restaurants: La Grande Table Marocaine and La Grande Table Française.

The hotel contains as well an underground tunnel system which the staff, dressed in “genie-like butlers” outfits, use to travel around the hotel unseen.

Royal Mansour has won many awards in recent years, cementing its status as one of the best hotels in Morocco, Africa, and worldwide. 

Just last week, the “Haute Grandeur Global Awards” ranked the manager of the Marrakech-based hotel, Jean-Claude Messant, as the Best General Manager in Africa.

In 2019, Royal Mansour prominently featured in the ranking of the American luxury and lifestyle travel magazine Conde Nast Traveler. The Marrakech-based establishment was ranked as the best hotel in Africa and the 6th best in the world.

Two years prior, Conde Nast Traveler Readers Travel Award selected the Moroccan hotel as the best hotel spa in the world.

In  a review about the hotel, Conde Nast Traveler described it as “a swoon-worthy showpiece of Moroccan decorative art.”

Royal Mansour is not the only Moroccan hotel to have garnered enthusiastic plaudits worldwide and won coveted international accolades.  

La Mamounia, also in Marrakech, has received many awards recently, and is one of the go-to hotels among high-profile tourists who visit Morocco.

Marrakech is known as the capital of Morocco’s thriving tourism industry, with more than 2 million tourists visiting the city’s historic medina every year.

source: moroccoworldnews 

About 1,000 workers from a variety of professions held a silent rally in Quebec City on Oct. 15 to protest against the province’s COVID-19 vaccination mandates.

Using the rallying cry “Code White,” an emergency colour code send out by health-care staff when they face a violent situation and need backup, the event called on front-line workers and first responders to stand together in solidarity and reject the Quebec government’s vaccine passport. 

Attendees including nurses, policemen, teachers, and military veterans locked arms and stood solemnly in silence for 10 minutes on Dufferin Terrace, a long wooden sidewalk next to the Château Frontenac hotel on the St. Lawrence River. 

Shawn Kuhn, a fully vaccinated senior at the University of Georgia who was majoring in exercise and sports science, died Oct. 11, more than six weeks after developing COVID symptoms.

Shawn Kuhn, 21, a senior majoring in exercise and sports science at the University of Georgia (UGA), died Oct. 11 from COVID complications, despite being fully vaccinated.

For the past six weeks, Kuhn had been in and out of three different hospitals, was placed in a medically induced coma and was put on a ventilator, his father said in a social media post on Oct. 10.

According to his obituary, which described him as an avid UGA Bulldog fan with a passion for serving others, Kuhn played on his high school’s soccer team and was a member of the school’s cross-country team.

At UGA, he was working toward a bachelor’s degree in exercise and sports science, and worked as a certified personal trainer at UGA’s Ramsey Student Center. He was a competitive fisherman who also enjoyed hiking.

“Shawn was one the most caring, helpful and fun [people] I’ve known and met at UGA,”  said Libby Buchanan, a UGA alum and Kuhn’s friend. “Since that day in 2018, Shawn and me have kept being friends. Anytime you were around Shawn, you couldn’t help but smile and laugh. He never spoke bad about anyone and only encouraged you to be the best.”

Breakthrough case numbers continue to rise

The latest data from the Centers for Disease Control and Prevention (CDC) show as of Oct. 4, 30,177 patients were hospitalized or died despite being fully vaccinated — a number the agency acknowledges is an undercount of all SARS-CoV-2 infections among fully vaccinated persons.

According to the CDC, a vaccine breakthrough case occurs when someone tests positive for COVID at least 14 days after being fully vaccinated.

According to the CDC’s website, people with vaccine breakthrough infections may spread the virus and infect others.

As of May 1, the CDC stopped tracking all COVID vaccine breakthrough cases — instead tracking only those breakthrough cases which result in hospitalization or death. The CDC said it made the change in order to “maximize the quality of data collected on cases of greatest clinical and public importance.”

More COVID breakthrough cases were reported in Pennsylvania, causing concern among health officials. In the past month, about 26% percent of the nearly 5,000 hospitalizations for COVID-related issues within the state of Pennsylvania, were among those who were fully vaccinated.

The Cleveland Clinic said 15% of all new COVID cases the clinic treated in September were breakthrough infections, with 10% of hospitalizations occurring in vaccinated individuals.

According to Cleveland Clinic officials, those who were vaccinated and ended up hospitalized were largely patients who were over the age of 65 or had significant underlying medical conditions.

“While no vaccine is 100% effective and we expect to see some breakthrough cases, the far majority of new cases we are seeing are still occurring in those who are unvaccinated,” Cleveland Clinic officials said in an emailThursday morning.

Only African country having a FTA with the US, Morocco Now is the future-proof platform to capture opportunities in a changing world for our US partners! Sustainable, Competitive, Well Proven and Agile in Times Square too!

Over the past 20 years, under the leadership of His Majesty King Mohammed VI, may God assist Him, Morocco developed excellent trade and transport infrastructure and is definitely on the right path of industrial take-off. Tanger Med, the 1st maritime connection in Africa and on the Mediterranean and the 20th worldwide as well as the automotive cluster, which knows the fastest growth rate in the world contribute strongly to the growth of Morocco’s exports which have increased by more than 150 billion MAD between 2010 and 2019, this illustrates Morocco’s development.

“Morocco Now” also responds to the challenges facing the global economy in making a transition to low-carbon production given the environmental emergencies, consumer pressure and the new regulations around the world. The crisis of COVID-19 pandemic has also led to the reorganization of the global value chains towards less global dependence and more regional integration.

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