The best laid schemes o’ mice an’ men gang aft a-gley.
voanews.com: New Zealand Prime Minister Tests Positive for COVID-19
Quote:
May 14, 2022
she has mild symptoms...
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The best laid schemes o’ mice an’ men gang aft a-gley.
voanews.com: New Zealand Prime Minister Tests Positive for COVID-19
Quote:
May 14, 2022
she has mild symptoms...
Dachsie comment.
In my May 5, 2022, posting number 3055 in this thread, I posted on this limiting the use of J&J Covid 19 "vaccine" because of blood clotting condition an Epoch Times article.
This article today posted is by Children's Defense and extensively hyperlinked in the original does a much more "fair and balanced" discussion of the REASONS and TIMING of this current regulatory action by the FDA.
As you will see from reading this article we can rule out FDA motivation based on overarching concerns for the health of the people. The FDA gives ridiculous reasons for this action and shows that their overarching concern is that everyone be pushed into taking some form of one of the 3 brands of vaccines in the USA. The fact is that all three of the vaccines cause blood clotting problems, although not necessarily the TTP condition. Strokes and heart attacks are also blood clotting conditions.
The FDA wants to MAKE IT APPEAR that they are doing the right thing for the right reason. Not possible for the FDA as we know it.
The more reasonable speculation is that they can restrict the least administered J&J jab without much reduction in the overall number of vaccines administered.
This is doing the fake good thing for a no-good wrong reason.
The FDA's actions and patterns of policy and regulation operate with their same usual and customary evil political motivations.
The money and the bad medicine will keep flowing and keep killing.
_________________________________
https://childrenshealthdefense.org/d...5-d16b110d2c43
05/06/22
•
COVID › News
FDA Limits Use of J&J Vaccine Over Blood Clotting Disorder, But Experts Say Pfizer, Moderna Shots Pose Similar Risk
The U.S. Food and Drug Administration on Thursday put strict limits on the use of Johnson & Johnson’s COVID-19 vaccine, citing the risk of a blood clotting condition, but experts say that Pfizer and Moderna pose similar risks.
By
Julie Comber, Ph.D.
https://childrenshealthdefense.org/w...re-800x417.jpg
The U.S. Food and Drug Administration (FDA) on Thursday put strict limits on the use of the Johnson & Johnson (J&J) COVID-19 vaccine, citing the risk of a blood-clotting condition the agency described as “rare and potentially life-threatening.”
In a statement Thursday, the FDA said the risk of vaccine recipients developing thrombosis with thrombocytopenia syndrome (TTS) after receiving the vaccine “warrants limiting the authorized use of the vaccine.”
The FDA said it has identified 60 cases of vaccine-induced thrombosis with thrombocytopenia syndrome, including nine deaths, out of about 18 million doses administered — although the condition is likely underreported.
Women 30 to 49 years old are at the highest risk of TTS from the J&J vaccine, with about eight cases per 1 million doses of vaccine administered, according to the FDA.
According to the latest data from the Vaccine Adverse Event Reporting System (VAERS), between Dec. 14, 2020, and April 29, 2022, there were 13,873 reports of blood-clotting disorders following COVID-19 vaccines in the U.S.
Of those, 6,227 reports were attributed to Pfizer, 4,943 reports to Moderna and 2,662 reports to J&J.
In the U.S., 575 million COVID-19 vaccine doses had been administered as of April 29, including 339 million doses of Pfizer, 217 million doses of Moderna and 19 million doses of J&J.
The agency said the “known and potential benefits” of the J&J vaccine for preventing COVID-19 outweigh the known and potential risks for individuals 18 and older “for whom other authorized or approved COVID-19 vaccines are not accessible or clinically appropriate,” or “who elect to receive the Janssen COVID-19 vaccine because they would otherwise not receive a COVID-19 vaccine.”
The agency described TTS as “a syndrome of rare and potentially life-threatening blood clots in combination with low levels of blood platelets with onset of symptoms approximately one to two weeks following administration of the Janssen [J&J] COVID-19 vaccine.”
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The updated restrictions to the Emergency Use Authorization (EUA) of the vaccine, marketed under the Janssen brand, also apply to booster doses, CNN reported.
People who can still get the Janssen vaccine include:
Those who had a severe allergic reaction to the Pfizer/BioNTech or Moderna mRNA vaccine.
Those with personal concerns about the mRNA vaccines who would remain unvaccinated unless they can choose the Janssen vaccine.
Those with limited access to mRNA COVID-19 vaccines.
Symptoms of TTS include shortness of breath, chest pain, leg swelling, persistent abdominal pain, neurological symptoms (like headaches or blurred vision) or red spots just under the skin called “petechiae” found beyond the site of injection.
Experts question timing, and why just J&J?
Peter Marks, M.D., Ph.D., director of the FDA’s Center for Biologics Evaluation and Research, said limiting the authorized use of the Janssen vaccine “demonstrates the robustness of our safety surveillance systems and our commitment to ensuring that science and data guide our decisions.”
Marks said:
“We’ve been closely monitoring the Janssen COVID-19 Vaccine and occurrence of TTS following its administration and have used updated information from our safety surveillance systems to revise the EUA.
“The agency will continue to monitor the safety of the Janssen COVID-19 Vaccine and all other vaccines, and as has been the case throughout the pandemic, will thoroughly evaluate new safety information.”
However, Brian Hooker, Ph.D., P.E., Children’s Health Defense chief scientific officer and professor of biology at Simpson University, had a different take on the news.
“It seems like the FDA pays lip service to the fact that the spike protein can cause clotting, and to the widespread reports of clotting, by punishing Janssen, who has become the ‘whipping boy’ of the COVID-19 vaccine manufacturers through the pandemic,” Hooker said.
“I believe this is partially because of the limited use of the Janssen vaccine in the U.S. as compared to Pfizer and Moderna,” he added.
Hooker said the FDA can limit the use of the J&J vaccine without significantly impacting vaccine distribution overall, “while having the appearance of addressing the myriad vaccine adverse events caused by all the types of COVID-19 vaccines.”
As of Thursday, CNN reported only 7.7% of those considered fully vaccinated received the J&J vaccine.
Dr. Pierre Kory, founder and president of Front Line COVID-19 Critical Care Alliance, told The Defender:
“My only hypothesis is this action is some attempt for the FDA to be able to claim that they took at least some action to protect the safety of the public, akin to ‘virtue signaling.’
“Having been a keen observer of their actions throughout the pandemic, I find this action to be completely insufficient and demonstrates a calculated attempt to ensure vaccinations with similarly dangerous vaccines continue.”
Dr. Meryl Nass questioned the timing of the FDA’s restriction of the EUA.
“Why did the FDA just throw the kill switch on the Janssen vaccine, when it knew of the thrombosis problems since the rollout?” Nass asked.
Nass told The Defender the FDA may have known about the thrombosis problem even before the Janssen vaccine rollout, “since the adenovirus vector platform is known to be associated with thrombosis” for “more than 15 years.”
Kory, who noted that all COVID-19 vaccines have had a high rate of adverse events, also questioned the timing of the new restrictions.
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“I find the timing of this action to be both irrational and alarming given there is extensive data from around the world, much of it being censored from media and medical journals, that all the COVID-19 vaccines, not just Janssen, have long had unacceptable and diverse toxicity signals — beyond just clotting disorders from numerous pharmacovigilance databases and epidemiological and public health data reports,” Kory said.
As far back as April 2021, U.S. and European health officials were investigating whether the J&J COVID-19 vaccines were causing blood clots.
However, there was already mounting evidence the Pfizer and Moderna vaccines could cause similar adverse reactions. U.S. regulatory officials were alerted to this risk as far back as December 2020.
The Centers for Disease Control and Prevention (CDC) in December 2021 recommended the Pfizer and Moderna mRNA COVID vaccines over the J&J vaccine due to the risk of blood clots, despite data showing the Pfizer and Moderna shots also cause blood-clotting disorders.
In January 2021, shortly after the rollout of Pfizer’s vaccine in the U.S., The Defender reported on the death of a 56-year-old Florida doctor who developed a blood-clotting disorder after the Pfizer vaccine and died 12 days later.
The Defender also reported on numerous other deaths related to blood-clotting disorders that developed after the Moderna and J&J vaccines.
The J&J vaccine received EUA on Feb. 27, 2021.
On April 13, 2021, the FDA and CDC paused use of the vaccine to investigate six reported cases of TTS.
The agencies lifted the pause only 10 days later, after confirming a total of 15 cases of TTS had been reported to VAERS, including the original six reported cases, out of approximately 8 million doses administered.
New VAERS Data as of May 6, 2022 (posted May 13, 2022)
30,372 Deaths and 1,435,555 Adverse Events
27,968 Pfizer/Moderna and 2,404 J&J Deaths
PLUS 1,348,352 Pfizer / Moderna and 87,203 J&J Adverse Events
Source: https://www.drtenpenny.com/newslette...comp-l3609csf2
I heard about this on this show this evening. There is later more alarming data.
https://www.theepochtimes.com/baby-f...ent=05-15-2022
Watch Joshua Phillip Epoch Times show for free.
Live Q&A: Baby Formula Crisis Caused by Government Chokehold; $350 Million in Secret Payments to Fauci and NIH Uncovered
Crossroads Crossroads
JOSHUA PHILIPP
There is a national shortage of infant formula, following an alleged bacterial outbreak at an Abbott plant in Michigan that led to recalls for three major brands. Yet, government restrictions on the infant formula industry may have played a part in the current crisis, as regulations created a bottleneck. And as this takes place, the U.S. government is allegedly providing infant formula for facilities processing the mass migration into the United States.
Meanwhile, the National Institutes of Health is acknowledging that secret payments received by its scientists, including Dr. Anthony Fauci, and leadership do look like conflicts of interest. This comes as more evidence emerges on ties between the NIH and virus labs in China; and amid new reports detailing how the Chinese leadership planned to use biological weapons in a hypothetical third world war against the United States.
And in other news, an FBI whistleblower recently stepped forward to Project Veritas to reveal how the agency is targeting news outlets.
In this live Q&A with Crossroads host Joshua Philipp, we’ll discuss these stories and others, and answer questions from the audience.
https://thetruedefender.com/foia-doc...llborn-babies/
FOIA Docs: Pfizer Causes Miscarriages and Stillborn Babies
Photo of Ava Garcia Ava Garcia December 24, 2021
Among the first reports handed over by Pfizer was a ‘Cumulative Analysis of Post-authorization Adverse Event Reports’ describing events reported to Pfizer up until February 2021. But were there any real and objective statements and results?
If the results were real, and Pfizer was really safe, reports of stillborn babies from all over the world would not be on the rise.
Netflix reality TV star Maya Vander told her fans last week of her devastating grief after she delivered a stillborn baby at 38 weeks of pregnancy on December 9.
“Yesterday was the hardest day of my life,” Vander, 39, posted on Instagram, with a picture of new baby clothes in a memory box she was taking home from hospital instead of her baby boy. “I always heard of it but never imagined I’ll be part of the statistics.”
“After her loss, she wrote in Insider magazine that she had felt less movement from the baby a few days before she learned her baby had died and also that her husband and two children were COVID-positive, although she had tested negative. She said the baby, who was “perfect” and weighed seven pounds and four ounces, would be autopsied,” Life Site News reported.
“There was a flurry of sympathetic news coverage about Vander’s loss, but not one article dared to ask burning questions: did COVID shots during her pregnancy have something to do with this baby’s death? Or did COVID have something to do with it, and the COVID shots failed?”
Here’s the data Pfizer denied to give out, calling upon the FOIA, when it was specifically requested by a group called Public Health and Medical Professionals for Transparency, after a judge ruled that the FDA and Pfizer would have to answer their FOIA requests. Among the first reports handed over by Pfizer was a “Cumulative Analysis of Post-authorization Adverse Event Reports” describing events reported to Pfizer up until February 2021.
“The drug behemoth received more than 150,000 serious adverse event reports within three months of rolling out its COVID shot, but here we will focus on Table 6 of the data on pregnant and lactating women who received the shots in the first few months of the rollout, which began December 11. Most of these women would have been healthcare workers because that was who the first rounds of shots went to. As the clinical trials preceding the rollout excluded pregnant women, these would have been the first pregnant and lactating women to have ever received the vaccines.
Table 6 states that of 270 “unique pregnancies” that were exposed to the vaccine, “no outcome was provided for 238 pregnancies.”
This leaves 32 pregnancies with known outcomes.
Pfizer’s report states that there were 23 spontaneous abortions (miscarriages), two premature births with neonatal death, two spontaneous abortions with intrauterine death, one spontaneous abortion with neonatal death, and one pregnancy with “normal outcome.” That means that of 32 pregnancies with known outcome, 28 resulted in fetal death.
Pfizer’s report states that there were five pregnancies with “outcome pending” as well as the 238 with “no outcome provided.” But 32 minus 28 equals four, not five.
Because of this confusion, I called Pfizer and emailed questions to their media rep. Were 28 of 32 known pregnancy outcomes actually fatal in the first 10 weeks that the vaccine became available, as their report suggests? That’s an 87.5 % pregnancy loss rate? And only one pregnancy outcome was “normal”? Please correct me if I’m wrong about this.
No reply.
The FDA would have had these data in their hands by the end of April. Maybe this is why they wanted to hide it for 55 years?
Ordinarily, when a new drug or medical device is put into action, the onus is, and should be, on the drugmaker to prove that any unexpected events that occur afterwards are not related to the product. “All spontaneous reports have an implied causal relationship as per regulatory guidance, regardless of the reporter’s assessment,” according to adverse event reporting guidelines. But Pfizer and the FDA ignored events with the temporal association and plausible cause for injury and have blithely declared the vaccine “safe and effective” for pregnant women.”
Allowed it to be mandated, even.
“Normally, it’s only five or six stillbirths every year. So, about one stillbirth every two months is the usual rate,” he said. “So, to suddenly get to 86 stillbirths in six months, that’s highly unusual. But, the most important confirmation that we have from the Waterloo, Ontario report was that all of the [mothers of the] 86 stillbirths were fully vaccinated,” Dr Daniel Nagase, an Alberta doctor who was ordered to leave his Alberta hospital for treating three COVID patients with ivermectin, stated for a local news report.
VigiBase data
Given the high numbers of doses given, the number of adverse events continues to climb. VigiBase, the database of the World Health Organization, reports pregnancy complications including:
* 3,952 spontaneous abortions
* 353 foetal deaths
* 189 missed abortions
* 166 premature labours
* 160 premature babies
* 154 abortions
* 150 slow movement of unborn baby
* 146 hemorrhages in pregnancy
* 132 premature deliveries
* 123 fetal growth restriction
* 120 stillbirths
* 105 ectopic pregnancies
* 90 pre-eclampsia
Another study that’s being heavily relied upon by the “experts” is from the New England Journal of Medicine.
“Initially the study was published with Table 4 showing “Spontaneous Abortion” after vaccination. The authors claimed that 104 pregnancy losses divided by 827 pregnancies resulted in 12.6% pregnancy loss rate, which is within a normal range. However, as Deanna McLeod, a professional cancer data analyst from Kaleidoscope Strategic Inc.in Toronto, and her colleagues pointed out in a letter to the NEJM, in the tiny print below the table was a statement that a “total of 700 participants received their first eligible dose in the third trimester.” Since the definition of spontaneous abortion pertains to pregnancy loss under 20 weeks gestation, that meant 700 women didn’t belong in the denominator because when they were vaccinated, they were already past the point of being able to have a spontaneous abortion. So, properly read, the fraction changed from 104/827 to 104/127 (81.9%). Hence, an 82% pregnancy loss rate for the first trimester pregnancies.”
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Schedule for May 16. All times EST.
8:45 AM – 9:55 AM: Panel 1: Efficacy of Non-Pharmaceutical Public Health Interventions Jay Bhattacharya (moderator), Aaron Kheriaty, Clare Craig, Eran Ben-David
9:55 AM – 10:45 AM: Panel 2: COVID-19’s Impact on Universities and Their Research and Teaching Missions Retsef Levi (moderator), David Shmoys, Chirag Patel
10:45 AM – 11:15 AM: Coffee Break
11:15 AM – 12:25 PM: Panel 3: Vaccine Efficacy, Safety Martin Kulldorff (moderator), Steve Kirsch, Neeraj Sood, Joe Fraiman, Retsef Levi
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2:40 PM – 3:10 PM: Coffee Break
3:10 PM – 4:15 PM Panel 5: The Way Forward Jay Bhattacharya (moderator), Robert Malone, Alex Washburne, Don Boudreaux
4.15 PM – 4.30 PM: Farewell comments
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The Summer of Rage & Continuation of the COVID War on America
https://tomrenz.substack.com/p/the-s...urce=email&s=r
Tom Renz
May 16 2022
COVID has a case fatality rates and reproduction rates that are, frankly, not really much worse than a bad flu season. Yet we are pushing untested death jabs that are killing millions, shut down our economy, printed $4 TRILLION+ dollars that devalued the dollar for working Americans and gave it all to billionaires, and masked our entire nation to deal with this. Why would anyone do this?
The answer is not apparent but quite clear if you investigate deeply enough, this is a war on America, and it is NOT the only front. Let’s look at what has happened since COVID and what is coming. When COVID began, we shut down almost all small and mid-sized businesses in America - the engine of our economy - while allowing big businesses (Walmart, Amazon, etc.) to stay open. This destroyed much of our middle class and transferred a MASSIVE amount of wealth to billionaires and away from the lower and middle classes.
While our businesses were closed, we saw months of riots, purportedly over the death of George Floyd. Regardless of how we feel about BLM or the Floyd PROTESTS, the riots were completely unacceptable but allowed to continue for months. In fact, while this was happening, instead of increasing law enforcement so legitimate protestors could do so safely and peacefully, we defunded the police in many places to allow for the law-breaking rioters to completely discredit any legitimacy there ever was to the real question of the realities of racism in law enforcement. Further, these riots destroyed numerous cities and small businesses (including minority businesses) and facilitated even more wealth transfer to the ruling rich by allowing them to snatch up more market-share and prime properties at a major discount.
Then we have the election. I do not care whether anyone reading this liked Trump or liked Biden, the reality is that this election was not safe and not secure. COVID was used as an excuse to alter election safeguards and procedures on a national level, and we now know conclusively that fraud did occur. Does this mean I can prove Donald Trump won; no, it does not. What I can say is that we did not have a fair and honest election and that it is quite suspicious that no one is considering the massive amounts of evidence (2000 Mules, Lindell, Pulitzer, etc.). If the machines were secure, then let us open them up, if the ballots were legitimate then let’s do an audit (not a recount), and if there is nothing to hide then let’s prove it so we can move on (unless there is something to hide). Regardless, the point is that the election is another example of an attack on America because, fraud or not, it has further divided us (and gave us the worst President in history).
With all that was happening, particularly including a terrible streak of PR for the death jabs, the President badly needed a distraction, so then we start on Ukraine. War is terrible and I always feel bad for the people suffering through war but isn’t it ironic that the same Democrats that had a conniption about the war in Iraq (where there were mind-boggling human rights abuses) simply could not stand by while a war occurred in Ukraine? The reality is that the Ukraine was the money-laundering capital for the global billionaire crowd and the attacks on Ukraine were attacks on the mega-rich (as well as Hunter Biden and “the big guy”) and that could not stand. At the same time Ukraine was a great distraction from the continual leak of truth about the death jabs and a phenomenal opportunity to print more money and launder it through Ukraine to the same corrupt billionaires (this is a whole other article). More inflation for Americans, more gifts to the rich.
After the election we started hearing about food shortages. These are not fully here yet, but they are coming. Right now, we have a baby formula shortage created by the FDA’s inexplicably long closure of one of the major producers of formula and shortages of raw materials due to policies implemented by the administration (all of which benefit billionaires while hurting the working class). Meanwhile, Biden is doing nothing about the moratorium on fertilizer shipments that Union Pacific and implemented, for literally no real reason, during the growing season. Union Pacific’s main owners are Blackrock and Vanguard and, let me assure you, the billionaires and leadership of the Chinese Communist Party (who control those companies) will not be going hungry but the lower- and middle-class American people will continue to see food prices skyrocket while many food items simply will not be available.
While much more is coming (new variants, the energy shortage, the currency collapse and financial crisis) the next immediate step is the “summer of rage”. Take a look at this:
https://substackcdn.com/image/fetch/...2291x3469.jpeg
Notice not only the search results but the search suggestions in Google. Now compare that with this:
https://substackcdn.com/image/fetch/..._2291x5214.png
Does this seem unbiased to anyone? The billionaires and the Anti-American crowd are now preparing for Roe v. Wade riots and if the SCOTUS does not overturn the case, they will find something else.
The important thing to understand is that all of this is about the war on America and our freedoms. A violent overthrow is not in anyone’s interests (Americans have too many guns) but the destruction of our nation through the destruction of our foundational values is absolutely occurring.
At this point we should be preparing for a “summer of rage”, the continued collapse of our financial system (inflation, gas prices, food prices, etc.), an upcoming energy crisis, and more new global diseases/variants. These “crises”, or similar “crises”, are coming. The question will be whether the American people simply stand and say no to this corruption or whether we lose our freedoms forever.
quote Dr. Pierre Kory
Rem Death Is Near
Despite disastrous results, Team Biden still pays hospitals to use remdesivir as primary Covid treatment
by: WorldTribune.com 05/16/2022 Source: WorldTribune.com
by WorldTribune Staff, May 15, 2022
The Biden administration is paying hospitals to use remdesivir as the primary treatment for Covid despite the drug being highly ineffective against the virus and routinely causing severe adverse reactions, a top physician noted.
"Despite its horrible track record, the U.S. government actually pays hospitals a 20% upcharge for sticking to the remdesivir protocol, plus an additional bonus. Hospitals must also use remdesivir if they want liability protection," Dr. Joseph Mercola wrote for The Defender on May 12.
"Incentives like these have turned U.S. hospitals into veritable death traps, as more effective and far safer drugs are not allowed, and hospitals are essentially forced to follow the recommendations of the U.S. Centers for Disease Control and Prevention," Mercola wrote.
Remdesivir is also an extremely expensive drug, costing between $2,340 and $3,120 depending on your insurance.
Ivermectin, meanwhile, which has been very effective against Covid and shown to outperform other drugs, costs between $48 and $94 for 20 pills depending on your location. The average cost is said to be about $58 per treatment.
Related: Idaho nurse: Covid patients ‘are not dying from Covid, they’re dying from the treatments’, November 29, 2021
In late April, the FDA approved remdesivir as the first and only Covid treatment for children under 12, including babies as young as 28 days. The drug is also approved for outpatient use in children.
It has been known for more than year that remdesivir is not an effective Covid treatment. The World Health Organization (WHO) in November 2020 advised against using it for Covid patients.
"Curiously, while Big Tech — aided and abetted by the U.S. government — has spent the last two years censoring and banning any information that doesn’t jibe with the opinions of the WHO, the U.S. government has completely ignored the WHO’s recommendation against remdesivir," Mercola noted.
Forbes science reporter JV Chamary noted in a January 2021 article titled “The Strange Story of Remdesivir, a COVID Drug That Doesn’t Work”:
“The drug proved ineffective against the Ebola virus … yet was still subsequently repurposed for SARS-CoV-2 coronavirus. News media prematurely reported that patients were responding to treatment. But the published data later showed that 'remdesivir was not associated with statistically significant clinical benefits [and] the numerical reduction in time to clinical improvement in those treated earlier requires confirmation in larger studies.' "
In an April 30 blog post, Dr. Meryl Nass raised concern about the FDA’s approval of remdesivir for outpatient use in babies, stating: “Remdesivir received an early EUA (May 1, 2020) and then a very early license (October 22, 2020) despite a paucity of evidence that it actually was helpful in the hospital setting. A variety of problems can arise in its secondary use, including liver inflammation, renal insufficiency and renal failure."
In fact, Mercola noted, all Covid treatment drugs recommended by U.S. health authorities and pushed by their allies in Big Media "have been disastrous in one way or another."
Paxlovid "will in some cases cause the infection to rebound when the medication is withdrawn," Mercola wrote. "Molnupiravir (sold under the brand name Lagevrio) also has serious safety concerns. Not only might it contribute to cancer and birth defects, it may also supercharge the rate at which the virus mutates inside the patient, resulting in newer and more resistant variants."
"The fact that U.S. health authorities have focused on these drugs to the exclusion of all others, including older drugs with high rates of effectiveness and superior safety profiles, sends a very disturbing message," Mercola wrote. "They’ve basically become extensions of the drug industry and have abandoned their original purpose, which is to protect public health — by ensuring the safety and efficacy of drugs, in the case of the FDA, and by conducting critical science and data analysis in the case of the CDC. Instead, they seem to be doing everything they can to protect Big Pharma profits, even if it costs you your life."
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Dachsie comment:
Dr. Naomi Wolf on vaccinated women's breast milk harming babies. No studies done.Baby milk formula deliberate shortage. Abbott labs only manufacturer of baby formula. You can't make BigPharma do the right thing for the right reason but BigPharma can certainly fake it.
Meanhwhile it just so happens that Bill Gates, baby killer par excellence, just happens to be johnny-on-the-spot to provide fake breast milk manufactured in the same evil laboratories at just the same time that the monopoly baby formula makers have experienced factory shutdown beyond their control.
How many children can BigTech and BigPharma and BigMedicine kill with this operation?
________________
https://americasbestpics.com/video/p...sdcdRukY9?s=cl
https://americasbestpics.com/video/sdcdRukY9?s=e
Prophetic Bill Gates Invests In Lab-Produced Breast Milk as Vaccinated Mothers' Babies Fail to Thrive Dr. Naomi Wolf: "We're seeing a lot of reports of newborns with vaccinated mothers who are having problems with lactation... They're going to the doctor, and the doctors are baffled; they don't know what's wrong. But of course, the babies are having failure to thrive or they're not gaining weight appropriately." "I also note that Bill Gates, and Jeff Bezos, and the usual suspects of big tech criminals are invested in something called BIOMILQ, which is a lab-grown replacement for breast milk, and I really raise this as a red flag because I do believe we're seeing a fully-coordinated attack on humanity." Problems With tion
https://www.reddit.com/r/banned4life...n_labproduced/
video 2:04 video runtime
Prophetic Bill Gates Invests In Lab-Produced Breast Milk as Vaccinated Mothers' Babies Fail to Thrive
Dr. Naomi Wolf: "We're seeing a lot of reports of newborns with vaccinated mothers who are having problems with lactation... They're going to the doctor, and the doctors are baffled; they don't know what's wrong. But of course, the babies are having failure to thrive or they're not gaining weight appropriately."
"I also note that Bill Gates, and Jeff Bezos, and the usual suspects of big tech criminals are invested in something called BIOMILQ, which is a lab-grown replacement for breast milk, and I really raise this as a red flag because I do believe we're seeing a fully-coordinated attack on humanity."
https://www.youtube.com/watch?v=yVPxp2PM3g0
https://www.youtube.com/watch?v=yVPxp2PM3g0
Sen. Ron Johnson & Dr. Peter McCullough Discuss Early C19 Treatment with Sean Spicer.
6:33 video runtime
39,800 views
Dec 2, 2020
1.4K
Association of American Physicians and Surgeons
Learn more and download guide at http://covidpatientguide.com/
_________________
https://www.youtube.com/watch?v=ucRn_pZVaDg
The Suppression of Early Treatment is Illegal, Unethical, and Immoral
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advance to 1:48
Sign the petition: https://interestofjustice.org/ Note: the petition link on the left is closed. Click the link on the right to sign the active petitionQuote:
Originally Posted by Dachsie
- Dr Mark Trozzi
- [May 13, 2022
Here is our best tool to urgently stop the most imminent threat against us: the proposed IHR amendments which are the WHO and WHA's back door to permanent global dictatorship.
Many of us have been studying the US proposed amendments to the International Health Regulations.
https://external-content.duckduckgo....jpg&f=1&nofb=1The WHO and WHA were hoping to qui etly pass these amendments while humanity was sleeping. These amendments are one of the WHO and WHA’s back door methods to clinch dictatorial control over all people of all nations, and create a supranational global government that supersedes our democratic sovereign authority over our own countries and lives.
What can we do about it on such short notice? They plan to sign this in their World Health Agency meeting in less than two weeks from May 22-28 in Geneva.
Just as young Arthur drew the sword from the rock, and all were surprised that this young lad was the champion they were waiting for; so too, Interest of Justice, a small human rights and legal activism group, has taken the effective lead on action to stop the tyrannical IHR amendment scheme. Let’s join the Interest of Justice now, and be big together.
The WHA is ignoring due process, and violating many laws if they pass this thing. Interest of Justice has done the hard work so we can all take the coordinated big action needed, quickly and easily. Not only are we insisting on due process, and justification for the amendments, we are also laying the ground work to sue the WHA and those participating with them if they do pass this. As well, we are underlining in bold red ink that the amendments are illegitimate, null and void; they were done without due process and a midst strong public outcry demanding transparency, justification, and details.
https://external-content.duckduckgo....ale&f=1&nofb=1
Xavier Becerra
With one click, your petition will reach many perpetrators of this wicked scheme including Tedros and others at the WHO and WHA, as well as US agents including Mr. Xavier Beccera who authored this treasonous document. Shutting this thing down within the US means stopping it at its source.
I can not over emphasize how important this particular mass action is. Please take a few minutes now to complete it.
Big thanks and support to legal action champions: Interest of Justice, an organization I have also now joined, and will help support.
Sign to stop IHR Amendments Now!https://drtrozzi.org/wp-content/uplo...s-then-who.png
Join The INTERNATIONAL LEGAL ACTION To STOP The Latest WHO' s Power Grab!
TO SIGN THE PETITION, visit: https://interestofjustice.org/
Summary regarding action against the IHR amendmentIt is also worthy for each of us around the world to communicate with our federal government representatives demanding that they stand against the WHO, stop the IHR amendment, as well as defund, exit and investigate the WHO. More about stopping the WHO and building a better future here: https://drtrozzi.org/2022/05/10/stop...better-future/
You will notice two actions on the Interest of Justice page. On the right is the extremely well strategically worded extensive petition that we are discussing. On the left is an additional opportunity to provide personal comments to the HHS and WHA about this, but that closes today May 13th. Signing the lengthy petition on the right is the most important action we can take right now.