Coronavirus

Just received this grocery store ad. This grocery story is about to go out of business. It's hard to see how this ad promotion of parents harming their young children will help this store sell more groceries. What could happen is that some of the kiddies could collapse and be seriously vaccine injured right there in their store. Then the store will be associated with harming children and that should shut down grocery sales for good.

https://ecp.yusercontent.com/mail?ur...C_jx7mUQ.g--~D

https://ecp.yusercontent.com/mail?ur...U3aVvEaMTw--~D

Boost your kids' defense
COVID Shots Now Recommended for Kids 3-4


Schedule Now

Schedule Now

https://ecp.yusercontent.com/mail?ur...nCM0zzr0Xw--~D


Know before you go
With at-home antigen and in-store molecular (NAAT) tests, you can get results for
COVID-19 in just 20 minutes.
Shop or Schedule

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https://ecp.yusercontent.com/mail?ur...Btf2MIOiUA--~D

https://www.youtube.com/watch?v=DK7IVxa5l8s


This is my second posting featuring Dr. John Jacobs. This is bombshell data. YouTube probably will spike this video very soon. This a few minutes more than the 1 minute trailer I posted earlier but full interview is still behind a pay wall on Epoch TV.
This video is premiering live right now but in a few minutes, the replay should be available with the same url. This was a VERY short video like maybe 10 minutes.

https://www.youtube.com/watch?v=DK7IVxa5l8s

87% of Trial Data Hidden from Medical Journals; Fmr FDA Director: Not Our Job to Correct Articles


Facts Matter with Roman Balmakov
782K subscribers

Content:

Dachsie comment:
Congressman Scalise held up a sign in congress a few days ago with the number 434 on it, saying Dr. Fauci has not testified on the House floor in over a year, 434 days.
Just pointing out that Fauci is hoping to slither out of his position very soon. He plans to just take the money and run.

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Top House Republican: 'Why Are They Hiding Dr. Fauci?'

https://www.youtube.com/watch?v=7bJeMyssEtQ

https://www.youtube.com/watch?v=7bJeMyssEtQ

6:47 video runtime

Forbes Breaking News


Jun 23, 2022

At today's House Select Committee of the Coronavirus, Rep. Steve Scalise (R-LA) called out the absence of Dr. Anthony Fauci from House hearings.

https://youtu.be/7bJeMyssEtQ?t=140

_____________________

https://www.republicanwhip.gov/news/...-hiding-fauci/

https://www.republicanwhip.gov/wp-co...o-1000x553.png

WASHINGTON, D.C. — House Republican Whip and Ranking Member of the Select Subcommittee on the Coronavirus Crisis Steve Scalise’s (R-La.) opening statement at today’s Select Subcommittee’s hearing calls out Democrats for refusing to investigate the Biden Administration’s horrific track record during the COVID-19 pandemic. Whip Scalise criticizes Democrats on the Select Subcommittee on the Coronavirus Crisis for failing to hold a hearing with President Biden’s Chief Medical Advisor, Dr. Anthony Fauci in over a year. Additionally, Whip Scalise urges Select Subcommittee Democrats to hold a hearing about the origins of the coronavirus and investigate claims that the Centers and Disease Control and Prevention (CDC) allowed teacher union bosses to re-write critical portions of the Biden Administration’s school reopening guidance, which effectively kept thousands of schools closed when they could have reopened.

“Thank you, Mr. Chairman.

“I would like to welcome Dr. Birx. Thank you for being here today.

“And thank you for your four decades of service to this country, including 29 years in the U.S. Army.

“Like Groundhog Day, my Democrat colleagues will use today to continue their political vendetta against the former Trump Administration while continuing to cover up the many failures that have occurred with respect to COVID-19 under the Biden Administration.

“It is our job to perform congressional oversight over the administration. That’s why Republicans on this Subcommittee have focused on serious issues like the CDC’s school reopening guidance and the emails that prove the Biden Administration colluded with union bosses to keep millions of American children locked out of their classrooms.

“We now know that the social isolation and closed schools caused by the COVID lockdowns resulted in serious mental health issues and dramatic learning loss for millions of America’s kids. The last time I tried to talk about this incredibly important issue, the Chairman urged us all to not look backward, stating:

“‘I would hope we won’t spend all of our time today talking about yesterday. I’m concerned about tomorrow and the day after.’ (14:53)

“He went on to say, ‘All of us can spend the rest of our lives talking about what happened before COVID-19, or we can spend a little time trying to figure out how best to move forward from whatever mistakes may have been made, whoever may have made them, or we can spend all of our time assigning blame.’ (47:39).

“But here we are today, having yet another hearing with a witness to discuss things that happened more than two years ago while working for the former president.

“No hearing with Biden’s first COVID-19 response coordinator and Dr. Birx’s immediate successor, Jeff Zeints.

“No hearing with Biden’s current coordinator, Dr. Ashish Jha.

“And no hearing in more than a year with Biden’s Chief Medical Advisor, Dr. Fauci.

“Of course, I welcome Dr. Birx’s testimony today, but I would be remiss if I didn’t point out the irony of the Chairman’s past statements against talking about the past. It is noteworthy that this Subcommittee would focus on the events of years ago while denying our ability to address the failures of the Biden Administration that are still occurring to this day.

“More Americans died from COVID during President Biden’s first year than Trump’s, even with multiple vaccines. And we are currently dealing with the serious impact COVID lockdown policies have had on millions of kids. I’m worried the effects will last for years to come, jeopardizing their future ability to achieve their dreams.

“We need a proper investigation into the origins of COVID. I have asked the Chairman for this many times and yet we still have not had a hearing to answer this question that millions of Americans keep asking.

“Again, begs the question of why this Select Subcommittee on Coronavirus refuses to hold a hearing on the origins of COVID-19 when the World Health Organization, and a growing list of leading experts in the scientific community all deem it worthy of investigation.

“Dr. Jeffrey Sachs of Columbia University who himself thinks this came from a lab said COVID-19 is ‘a blunder of biotech not a natural spillover.’

“And now it is being reported that Dr. Tedros, the head of the WHO, is quietly confiding to officials that he believes this pandemic originated in a lab in China.

“I wonder if Dr. Sachs and Dr. Tedros are—to use the Chairman’s own words—‘us[ing] the issue of the origin of the virus to shift accountability from President Trump to Dr. Anthony Fauci,’ as he accused Republicans of doing.

“More than one million Americans have died from COVID. We should understand how this virus started not only because we owe it to those that have died but also to protect against future pandemics. China was doing risky research in a lab that likely caused this pandemic. Did China lie to the world about the virus and how it spread? These are questions we should absolutely know the answers to.

“To that end, I know Dr. Birx has told us before that the origins of the virus are detectable if China would be willing to share the earliest sequences of the virus. And Dr. Birx has previously said that early statements from scientists, scientific publications, and the media downplaying the lab leak were premature and not based on data.

“I’m glad we’ll get the opportunity to hear what she has to say about China’s involvement and how the U.S. and the rest of the world were misled by China and the World Health Organization.

“I also look forward to hearing Dr. Birx’s suggestions for reforming the CDC. Over the course of the pandemic, Americans have lost trust in what was once a premier public health organization. Their failures must be confronted in order for that trust to be restored.


“Thank you, Mr. Chairman. I yield back.”

Dachsie comment:

Even though Dr. Debby is no longer in government, she's still able to dissemble with the best of them.

I was able to listen the full 6 minutes though use of the word "utilize" usually makes me quit.

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https://www.youtube.com/watch?v=-GE62rNmXfA

https://www.youtube.com/watch?v=-GE62rNmXfA

Should The United States Be In The World Health Organization?': Jim Jordan Grills Dr. Birx

6:34 video runtime

Jun 23, 2022

Forbes Breaking News

At today's House Select Committee on the Coronavirus, Rep. Jim Jordan (R-OH) questioned Dr. Deborah Birx.

Dachsie comment:
With the release of more pages of documents at the first of each month, it is made ever more clear to us just how very corrupt Pfizer and the FDA are.

_________________________


https://childrenshealthdefense.org/d...9-9b303d83b1db


06/21/22
•

COVID › News
Pfizer Classified Almost All Severe Adverse Events During COVID Vaccine Trials ‘Not Related to Shots’

The case reports included in Pfizer clinical trial documents, released June 1 by the U.S. Food and Drug Administration, reveal a trend of classifying almost all adverse events — and in particular severe adverse events — as being “not related” to the vaccine.
By
Michael Nevradakis, Ph.D.

https://childrenshealthdefense.org/w...re-800x417.jpg

[SIZE=3]The latest release by the U.S. Food and Drug Administration (FDA) of Pfizer-BioNTech COVID-19 vaccine documents reveals numerous instances of participants who sustained severe adverse events during Phase 3 trials. Some of these participants withdrew from the trials, some were dropped and some died.

The 80,000-page document cache includes an extensive set of Case Report Forms (CRFs) from Pfizer Phase 3 trials conducted at various locations in the U.S., in addition to other documentation pertaining to participants in Pfizer-BioNTech vaccine trials in the U.S. and worldwide.

The FDA on June 1 released the documents, which pertain to the Emergency Use Authorization (EUA) of the vaccine, as part of a court-ordered disclosure schedule stemming from an expedited Freedom of Information Act (FOIA) request filed in August 2021.

Public Health and Medical Professionals for Transparency (PHMPT), a group of doctors and public health professionals, submitted the FOIA request.

CRFs show deaths, severe reactions to the vaccines during Phase 3 trials

The CRFs included in this month’s documents contain often vague explanations of the specific symptoms experienced by the trial participants.

They also reveal a trend of classifying almost all adverse events — and in particular severe adverse events (SAEs) — as being “not related” to the vaccine.

For example:

A female in her early 50s (randomization number 86545) who participated in the trial at the Sterling Research Group in Cincinnati, Ohio, died of an apparent myocardial infarction on Nov. 4, 2020. She had received two doses of the vaccine, on Sept. 10 and Sept. 29, 2020.

The patient had a medical history of chronic obstructive pulmonary disease, hypertension, hypothyroidism, osteoarthritis of the knees and attention deficit disorder. Her death was listed as “not related” to the vaccine, and was instead attributed to “hypertensive cardiovascular disease.”

A female in her late 50s (randomization number 220496), who participated in the trial at Cincinnati Children’s Hospital Medical Center, died of cardiac arrest on Oct. 21, 2020. Her death, however, was indicated as “not related” to her vaccinations (which occurred on July 30, 2020, and Aug. 20, 2020) as it “occurred 2 months after last receipt of study agent,” according to her CRF.

The participant’s medical history included obesity, placement of a gastric sleeve, gastroesophageal reflux, sleep apnea, supraventricular tachycardia, hypothyroidism, depression and asthma.

A male in his mid-60s (randomization number 221076) who participated in the trial operated by the Texas-based Ventavia Research Group died of an apparent myocardial infarction on Nov. 28, 2020. He had received the two doses of the vaccine on July 31, 2020, and Aug. 19, 2020.

The participant had a medical history that included a previous myocardial infarction, high blood pressure, high cholesterol, anxiety, bilateral hip pain, type 2 diabetes, fluid retention, angina (intermittent), restless leg syndrome, Vitamin D deficiency, tobacco dependency and the placement of a coronary arterial stent in 2017.

According to the CRF, he sustained the myocardial infarction on Oct. 27, 2020, and was diagnosed with pneumonia the following day. While both diagnoses were classified as “serious” in his CRF, they were both listed as “not related” to the vaccination, with his myocardial infection attributed to a “failed cardiac stent” and the pneumonia simply attributed to “infection.”

A female in her teens (randomization number 104650) was diagnosed with right lower extremity deep vein thrombosis on Nov. 15, 2020, which was still ongoing as of Mar. 29, 2021, the date of the CRF. She was hospitalized and her condition was classified as “serious,” but it was indicated as “not related” to the vaccine, instead attributed to a “fracture” occurring prior to her vaccination on Sept. 11, 2020.

The patient had a medical history including asthma, attention deficit hyperactivity disorder, Charcot-Marie-Tooth disease and obesity.

A male in his mid-70s (randomization number 227629) participating in the trial at Clinical Neuroscience Solutions Inc. (operating in Florida and Tennessee) sustained a series of adverse events following his vaccinations on Aug. 13 and Oct. 7, 2020.

He was diagnosed with COVID-19 on Aug. 30, 2020, which coincided with several other diagnoses classified as “serious,” including abdominal adhesions (Aug. 29, 2020), altered mental status (Aug. 29, 2020, lasting through Sept. 16, 2020), and acute hypoxic respiratory failure (Aug. 30, 2020). These diagnoses required his hospitalization.

He was also listed as having suffered from congestive heart failure on Aug. 30, 2020, but this diagnosis was listed as “not serious” and as “not related” to the vaccine, but to “prior surgery,” with no further details given. Similarly, his other serious adverse events were listed as being related to “prior” or “previous” surgery, or to “concomitant non-drug treatment.”

Other “non-serious” adverse events listed in this patient’s CRF include hypokalemia, anemia, acute renal failure, sepsis, hyponatremia, leukopenia, small bowel obstruction, aspiration pneumonia, mild concentric left ventricular hypertrophy (symptoms of which were still ongoing as of the CRF date of Mar. 29, 2021) and urinary tract infection.

The patient had a medical history encompassing ongoing hypertension, hypercholesterolemia, gastroesophageal reflux disease, constipation, hiatal hernia and previous diagnoses of small bowel resection, small bowel perforation, inguinal hernia, osteoarthritis in both knees and knee replacement (both knees).

A male in his mid-70s (randomization number 266982) participating in the trial at Boston Medical Center suffered a series of adverse events following vaccination, including pneumonia and peripheral edema. He had received two doses of the vaccine, on Oct. 2, 2020, and Oct. 27, 2020.

The patient was hospitalized for pneumonia on Jan. 20, 2021, in an event classified as “serious” but also as “not related” to the vaccine. However, the cause of his pneumonia was listed in the CRF simply as “un-related to vaccine,” while his peripheral edema diagnosis was attributed to “existing neuropathy.”

During his hospitalization with pneumonia, his blood pressure was measured as high as 179/72, with a heart rate reaching 105 beats per minute and an oxygen saturation level that fell to 92.0. In total, he had three emergency room visits during the observation period.

The patient had a medical history that included type 2 diabetes, alcoholic cirrhosis, hypothyroidism, asthma, sleep apnea, hypertension, diabetic neuropathy, congestive heart failure, generalized anxiety disorder, depression, insomnia, excessive urination, chronic obstructive pulmonary disease and HIV-positive status.

A protocol deviation also occurred involving this patient, as his diary was not activated following administration of the first dose of the vaccine.

A male in his early 40s (randomization number 68489) who participated in the trial at Cincinnati Children’s Hospital Medical Center sustained chronic myelogenous leukemia on Sept. 24, 2020, with the condition ongoing as of the date of the CRF on Mar. 29, 2021.

This was classified as a “serious” and “life-threatening” adverse event, albeit one that did not require hospitalization, but it was listed as “not related” to the vaccination but instead to a “genetic change in stem cells.”

The patient had been vaccinated on Aug. 26, 2020, and Sept. 17, 2020, and had a medical history of asthma and seasonal allergies. Other “non-serious” adverse events he sustained included leukocytosis and thrombocytosis.

A female in her mid-40s (randomization number 49018) who participated in the trial at Clinical Neuroscience Solutions Inc. was diagnosed with kidney stones on Jan. 4, 2021.

This was classified as a “serious” adverse event that required hospitalization, but was listed as “not related” to the vaccine, instead being related, again, to “kidney stone” (sic). She had received the two doses of the vaccine on Aug. 17, 2020, and Sept. 8, 2020.

The patient was diagnosed with COVID-19 on Jan. 27, 2021. Her prior medical history included migraine headaches, hypercholesterolemia and a Tarlov cyst.

A female approximately 30 years old (randomization number 53307) participating in the trial at Boston Medical Center, with nothing to report in her medical history, sustained a shoulder injury related to vaccine administration (SIRVA) on Sept. 9, 2020, with symptoms continuing until Feb. 8, 2021.

This injury was listed as being related to the second dose of the vaccine, which she received on Sept. 9, 2020 (she had previously received her first dose on Aug. 17, 2020).

A female in her late 50s (randomization number 260125) participating in the trial at Clinical Neuroscience Solutions Inc., suffered from acute exacerbation of asthma. The symptoms appeared in mid-December 2020, following her vaccination on Sept. 16, 2020, and Oct. 5, 2020.

Her symptoms were classified as serious but not life-threatening, and she was hospitalized. However, her asthma symptoms were listed as “not related” to the vaccine, instead being related to “asthma” with no further explanation provided. On Jan. 12, 2021, her blood pressure was recorded as 183/130, with a heart rate of 98 beats per minute.

Other less serious adverse events sustained by the patient included injection site pain, body pain, chills and a low-grade fever.

Her medical history included cholecystitis (and a cholecystectomy), herniated disc, total abdominal hysterectomy, bilateral oophorectomy, bilateral salpingectomy, endometriosis, hypertension, hypercholesterolemia, rheumatoid arthritis in remission, asthma, seasonal allergies, irritable bowel syndrome and obesity.

A male in his late 20s (randomization number 48413) who participated in the trial at Clinical Neuroscience Solutions Inc., sustained a bilateral pulmonary embolism on Dec. 14, 2020, with symptoms still ongoing as of the CRF date of Mar. 29, 2021.

This was listed as a “serious” adverse event that required hospitalization, but was attributed to the patient’s habit of vaping and his “sedentary lifestyle.” He had received the two doses of the vaccine on Aug. 13, 2020, and Sept. 2, 2020.

Other post-vaccination symptoms listed for the patient included fever, fatigue, headache, chills, vomiting, diarrhea, new/worsened muscle pain, new/worsened joint pain and swelling.

The patient had a medical history that included elevated triglycerides, genital herpes and seasonal allergies, in addition to a vaping habit.

The many serious adverse events – and several deaths – recorded during the Phase 3 trials are also apparent in a separate, massive document, exceeding 2,500 pages, cataloging such adverse events.

This document lists a wide range of adverse events suffered by trial participants classified as toxicity level 4 — the highest and most serious such level.

However, not one of the level 4 (most severe) adverse events listed in this particular document is classified as being related to the vaccination.

Level 4 adverse events listed in the document include but are not limited to the following, many of which occurred in multiple patients:

Acute cholecystitis
Acute respiratory failure
Adrenal carcinoma
Anaphylactic shock
Aortic valve incompetence
Appendicitis
Arrhythmia, supraventricular
Arteriosclerosis
Brain abscess
Cardiac arrest
Chronic myeloid leukemia
Complicated appendicitis/acute appendicitis with necrosis
Congenital heart disease/heart anomaly
Coronary artery occlusion
COVID-19 illness
Deep vein thrombosis
Diverticulitis
Hemiplegic migraine
Hemorrhagic stroke
Interstitial lung disease
Myocardial infarction
Orthostatic hypotension/possible postural hypotension
Osteoarthritis
Pericolic abscess
Peritoneal abscess
Renal colic
Ruptured diverticulum
Small bowel obstruction/small intestinal obstruction
Spontaneous coronary artery dissection
Subarachnoid hemorrhage
Suicidal ideation (and suicidal ideation with attempt)
Syncope
Type 2 diabetes
Worsening of abdominal pain
An “unevaluable event/“unknown of unknown origin”

Similarly, only a small number of toxicity level 3 adverse events were indicated as having been “related” to vaccination. Such adverse events included but are not limited to the following, some of which occurred in multiple trial participants:

Arthralgia
Blood glucose increase/glucose spike
Deafness/hearing loss
Dyspepsia
Hypotension
Lymph node pain
Lymphadenopathy/lymph node swelling
Musculoskeletal chest pain (non-cardiac)
Neutropenia
Pain in fingers/bilateral hands
Pruritus
Pyrexia/febrile syndrome
Severe headache
Shoulder injury related to vaccine administration
Sleep disorder/sleep disturbance
Tachycardia
Urticaria
Ventricular arrhythmia
Vertigo

Page 2,525 of the document in question also lists six trial participant deaths, with causes of death including arteriosclerosis, cardiac arrest, hemorrhagic stroke and myocardial infarction.

The small number of adverse events listed as being connected to the vaccine follows a trend noted in the previous tranche of Pfizer-BioNTech documents, released in May.

An additional document released in this month’s tranche catalogs patients who discontinued their participation in the Phase 3 trial, or whose participation was discontinued by physicians or other medical professionals.

While many patients were discontinued because they could not be located, because of a physician’s orders, because they moved to another region or for other personal reasons, numerous patients ended their participation due to adverse events, including but not limited to the following symptoms:

Acute myocardial infarction
Amnesia
Anorexia
Atrial fibrillation
Cerebral infarction
Congestive cardiac failure
Coronary artery disease
Deafness (unilateral)
Depression
Diabetic foot
Diverticular perforation
Exposure during pregnancy
Eye pain
Gait instability
Gastric adenocarcinoma
Gastrointestinal hemorrhage
Hypertension
Irregular heart rate
Loss of taste and smell
Myalgia
Paraparesis
Parkinsonism
Presyncope
Pulmonary embolism
Pyrexia
Swelling face
Tachycardia
Transient ischaemic attack
Urticaria
Vaccine allergy
Vertigo

In other instances, subjects withdrew because of fears connected to safety concerns related to the vaccine, or discomfort in receiving the second dose.

Clinical review document glosses over adverse events during trials

Also included in June’s FDA document dump was a 334-page “clinical review” document, which appears to have been approved by the FDA on Apr. 30, 2021, and which presents “pivotal data” from Phase 1/2/3 Study C4591001, conducted in the U.S., along with “supporting” Phase 1/2 data from Study BNT162-01, performed in Germany.

This document refers to both Pfizer-BioNTech vaccine, which received an EUA from the FDA, and the Pfizer Comirnaty vaccine, which received full FDA approval but is reportedly almost impossible to find at vaccination locations in the U.S.

As previously reported by The Defender, a federal judge found the Pfizer-BioNTech and Pfizer Comirnaty vaccines are legally distinct.

The clinical review document states:

“BNT162b2 has received temporary authorizations for emergency supply in 28 countries and conditional marketing authorizations in 39 countries globally.

“The name of the product supplied under emergency/temporary use authorization for all applicable regions is Pfizer-BioNTech COVID-19 Vaccine.

“The name of the product supplied under conditional marketing authorization for all applicable regions is COMIRNATY [COVID-19 mRNA Vaccine (nucleoside modified)].”

The document states that trial participants were administered one of two candidate vaccines, labeled BNT162b1 and BNT162b2 (the latter of which ultimately received an EUA from the FDA), or a placebo. A variety of dosage levels were also tested, ranging from 10 μg to 100 μg for BNT162b1, and 10 μg to 30 μg for BNT162b2.

In Phase 1 of Study BNT162-01, the clinical review reports that “40% to 45% of participants who received BNT162b1 and BNT162b2 across age groups and across dose levels reported one or more AEs [adverse events] from Dose 1 through 28 days (i.e., 1 month) after Dose 2.”

In what will turn out to be a general pattern throughout the clinical review, we are told that “most AEs were considered by the investigator as not related to study intervention and mild to moderate in severity, and all AEs were reported as resolved.”

Some specific adverse events highlighted in this part of the clinical review include:

“Among BNT162b1 recipients, 1 younger participant in the 10 μg group discontinued the study due to a moderate AE of malaise (considered as not related to study intervention) after Dose 1 and 1 younger participant in the 60 μg group discontinued due to a dose-limiting toxicity of pyrexia after Dose 1.

“One older participant in the 20 μg group had an SAE of severe syncope (considered as not related to study intervention) after Dose 1 and study treatment was withdrawn.

“Among BNT162b2 recipients, 1 younger participant in the 10 μg group discontinued the study due to a moderate AE of nasopharyngitis (considered as not related to study intervention) after Dose 1.

“One older participant in the 20 μg group had an SAE of ankle fracture (considered as not related to study intervention) after receiving both doses, was listed as recovering, and remains in follow-up.”

The clinical review also states “no deaths occurred in the Phase 1 part of Study BNT162-01.”

The review adds that “from Dose 1 of BNT162b2 30 μg to the unblinding date, 6 (50.0%) participants in the younger age group and 3 (25.0%) participants in the older age group reported at least 1 AE.”

Specifically, in this portion of the study, “two (16.7%) participants in the BNT162b2 30 μg younger age group and 1 (8.3%) participant in the BNT162b2 30 μg older age group reported at least 1 severe AE,” and “in the BNT162b2 30 μg younger age group, 3 (25.0%) participants reported at least 1 related AE and 1 (8.3%) participant reported 1 severe SAE.”

These specific adverse events, according to the review, were reported in “the system organ class (SOC) of nervous system disorders (3 [25.0%] participants in the younger age group and 1 [8.3%] participant in the older age group), followed by musculoskeletal and connective tissue disorders (1 [8.3%] participant in each age group). All AEs by preferred term (PT) were reported by no more than 1 participant.”

The review adds, “from Dose 1 to the unblinding date, 1 participant in the BNT162b2 30 μg younger age group reported a severe SAE (neuritis) that was assessed by the investigator as not related to study intervention,” and “there were no Phase 1 participants randomized to BNT162b2 30 μg or corresponding placebo who died through the data cutoff date of 13 March 2021.”

Review of results from Study C4591001

While “incidences in the BNT162b2 and placebo were similar within the age groups for younger (9.1% vs 11.1%) and older (4.3% vs 8.9%) participants, among those who received BNT162b2 instead of the placebo, “two severe events of myalgia and gastric adenocarcinoma (which was also an SAE) were reported for 2 participants in the … younger age group, both assessed by the investigator as not related to study intervention.”

It is further mentioned that “the only discontinuation due to an AE during this time was the participant in the BNT162b2 younger age group who reported an SAE of gastric adenocarcinoma (discontinued from the study on Day 23 after Dose 1 of BNT162b2).”

Ultimately, from dose 1 to 1 month after dose 2 for participants during the blinded safety follow-up of study C4591001, “the numbers of overall participants who reported at least 1 AE and at least 1 related AE were higher in the BNT162b2 group (30.2% and 23.9%, respectively) as compared with the placebo group (13.9% and 6.0%, respectively).”

Specifically, “severe AEs were reported by 1.2% and 0.7% in in the BNT162b2 and placebo groups respectively, and life-threatening AEs were similar (0.1% in both groups),” and “SAEs and “AEs leading to withdrawal were reported by ≤0.6% and ≤0.2%, respectively, in

both groups,” while “discontinuations due to related AEs were reported in 13 participants in the BNT162b2 group and 11 participants in the placebo group (0.1% in both groups).”

Overall, as reported for this part of the study, “in the younger age group, the number of participants who reported at least 1 AE from Dose 1 to 1 month after Dose 2 was 4233 (32.6%) and 1871 (14.4%) in the BNT162b2 and placebo groups, respectively. In the older age group, the number of participants who reported at least 1 AE from Dose 1 to 1 month after Dose 2 was 2384 (26.7%) and 1177 (13.2%) in the BNT162b2 and placebo groups, respectively.”

The review specifies that “the most frequently reported AEs in the BNT162b2 group … were injection site pain (2915 [13.3%]), pyrexia (1517 [6.9%]), fatigue (1463 [6.7%]), chills (1365 [6.2%]), headache (1339 [6.1%]), and myalgia (1239 [5.7%]),” however, some more serious adverse events that were reported during this stage of the trial included facial paralysis, cardiac disorders, hepatic cirrhosis, cholecystitis/cholecystitis acute, biliary colic, bile duct stone, biliary dyskinesia, lymphadenopathy, appendicitis, optic neuritis and hypersensitivity/anaphylaxis.

Overall, according to the review, “from Dose 1 to 1 month after Dose 2, severe AEs reported during the blinded follow-up period were low in frequency, reported in 1.2% of BNT162b2 recipients and 0.7% of placebo recipients.”

During the “open-label follow-up period,” referring to the period when the initial trial has been completed but participants are invited to continue taking the study drug for an additional period, the review states “three participants originally randomized to BNT162b2 died during open-label follow-up.”

While one of these deaths was reportedly due to a road accident, the other two were attributed to lung metastases and myocardial infarction. However, none of these deaths “were assessed by the investigator as related to study intervention.”

Furthermore, according to the report, during this period “there were 12,006 participants who had at least 6 months of follow-up. Among these, 3,454 participants (28.8%) reported at least 1 AE and 2245 participants (18.7%) reported at least 1 related AE. Severe AEs and SAEs were reported by 2.1% and 1.6%, respectively.”

The review provides data for participants from dose 3 (first dose of BNT162b2) to the data cutoff date. The severe adverse event incidence rate (IR) was 6.0 per 100 PY (patient-years), with specific conditions reported including pulmonary embolisms, thrombosis, urticaria, a cerebrovascular accident and COVID-19 pneumonia.

Here, the review adds that the IR for original placebo participants who had at least 1 life-threatening AE from Dose 3 to the data cutoff date was 0.5 per 100 PY. Only one such life-threatening event, an instance of anaphylactoid reaction, was considered to be related to the vaccination. Other life-threatening, serious adverse events included cardio-respiratory arrest, gastrointestinal necrosis, deep vein thrombosis and pulmonary embolism.

The report also notes, “There were 15 deaths in the BNT162b2 group and 14 deaths in the placebo group from Dose 1 to the unblinding date during the blinded placebo-controlled follow-up period.”

However, the report does not appear to go into detail about the causes of death for either group, other than to state, “None of these deaths were assessed by the investigator as related to study intervention.”

In the “Blinded Follow-Up Period from Dose 1 Through 1 Month After Dose 2,” in the BNT162b2 group, “SAE [serious adverse events] was similar in the BNT162b2 group (0.6%) and in the placebo group (0.5%),” with three SAEs in the non-placebo group deemed to be related to the vaccine. These included ventricular arrhythmia, lymphadenopathy and SIRVA.

During the “open-label follow-up period” for “original BNT162b2 participants,” the report states “one younger participant with no past medical history had a life-threatening SAE of myocardial infarction 71 days after Dose 2 that was assessed by the investigator as related to study intervention.”

However, despite its life-threatening nature, this condition “lasted 1 day and resolved the same day.”

Overall, “from Dose 1 to 6 months after Dose 2, during the blinded and open-label follow-up periods, 190 (1.6%) participants in the BNT162b2 group reported at least 1 SAE,” and “the number of participants who reported at least 1 SAE was 73 (1.1%) and 117 (2.2%) in the younger and older age groups, respectively.”

These SAEs were categorized as neoplasms, infections and infestations, gastrointestinal disorders, hepatobiliary disorders, respiratory/thoracic/mediastinal disorders and injury/poisoning/procedural complications.

An original placebo participant who received BNT162b2 for Dose 3 experienced a severe adverse event that “was assessed by the investigator as related to study intervention; specifically, “an anaphylactoid reaction 2 days post Dose 3” leading to the participant’s withdrawal from the study, despite a reported resolution.

A separate subsection in the report specifically addressed cases of Bell’s palsy and facial paralysis among trial participants. Specifically, “during the blinded placebo-controlled follow-up period, 6 participants developed one-sided facial paralysis (Bell’s palsy): 4 were randomized to BNT162b2 (all male) and 2 were randomized to placebo (1 male; 1 female),” according to the review.

Regarding the four vaccinated trial participants, their ages ranged from 40 to 70, with symptoms appearing three to 48 days after their last dose. Their symptoms were recorded as “mild to moderate in severity,” with duration ranging “from 3 to 68 days,” and with two of these cases “considered by the investigator to be related to study intervention.”



SNIP article a bit too long to post in one posting. Important to read all at original source

Dachsie comment:

In response to posting #3325 earlier today, Dachsie deems the following deserving of the MOC award (Most Outrageous Case).

"• A male in his mid-70s (randomization number 227629) participating in the trial at Clinical Neuroscience Solutions Inc. (operating in Florida and Tennessee) sustained a series of adverse events following his vaccinations on Aug. 13 and Oct. 7, 2020.


He was diagnosed with COVID-19 on Aug. 30, 2020, which coincided with several other diagnoses classified as “serious,” including abdominal adhesions (Aug. 29, 2020), altered mental status (Aug. 29, 2020, lasting through Sept. 16, 2020), and acute hypoxic respiratory failure (Aug. 30, 2020). These diagnoses required his hospitalization.
[/COLOR]
He was also listed as having suffered from congestive heart failure on Aug. 30, 2020, but this diagnosis was listed as “not serious” and as “not related” to the vaccine, but to “prior surgery,” with no further details given. Similarly, his other serious adverse events were listed as being related to “prior” or “previous” surgery, or to “concomitant non-drug treatment.”

Other “non-serious” adverse events listed in this patient’s CRF include hypokalemia, anemia, acute renal failure, sepsis, hyponatremia, leukopenia, small bowel obstruction, aspiration pneumonia, mild concentric left ventricular hypertrophy (symptoms of which were still ongoing as of the CRF date of Mar. 29, 2021) and urinary tract infection."

https://static-3.bitchute.com/live/c...Ei_320x180.jpg

https://www.bitchute.com/video/6QC3KGmvTyiF/

Miss BRAZIL (27yo Gleycy Correria) DEAD After Suffering Brain Hemorrhage & HEART ATTACK

Miss Brazil, Age 27, suffers brain hemorrhage and heart attack after tonsillectomy.

Died after a tonsillitis operation? Hmmm....OK. 27yo Miss Brazil: Gleycy Correria - Dead After Suffering A Brain Hemorrhage & Heart Attack ....and YES she was quaxxinated.

https://www.americaoutloud.com/the-w...ew-sars-cov-2/

The Warning Signs Make Monkeypox the New SARS-CoV-2

by Peter Breggin MD and Ginger Ross Breggin | Jun 26, 2022 | Health, Politics, World

https://www.americaoutloud.com/wp-co...and-covid.jpeg

My mom used to always say, “practice makes perfect.” Despite complaining, my siblings and I learned that doing something repeatedly develops judgment, skills, knowledge, good instincts, and a much better final product. Our products improved when we learned to evaluate our mistakes and not repeat them. So, let’s consider how we are doing two and a half years after the advent of COVID.

A New Disease Outbreak

Pride month has been declared for June in the United States, and Pride is celebrated in many parts of the world, in parades and great gatherings, and parties in the US, Europe, and other locations. Hundreds of thousands are celebrating.1

Unfortunately, there is an outbreak of monkeypox that has specifically been infecting Pride participants–“men who have sex with men,” –as the legacy media put it. The outbreak was first reported in May when a single case was detected in the UK.2

Scientists are now reporting that this outbreak of monkeypox is mutating at an unprecedented, accelerated rate compared to other outbreaks and is the “largest monkeypox virus (MPXV) outbreak described so far in non-endemic countries.3 Ever. As of June 23rd, more than 3,417 identified cases were reported across fifty-eight countries on multiple continents.4

Is Monkeypox a PHEIC (pronounced FAKE) Yet?

The World Health Organization (WHO) just called a meeting to determine if the monkeypox outbreak should be classified as a Public Health Emergency of International Concern.5 The emergency status “known as PHEIC — pronounced ‘fake’ — applies to an extraordinary event that carries a public health risk via the international spread of a disease, and one that potentially requires a coordinated response.”6 The last time WHO called a meeting to consider classifying a disease as a PHEIC was in January of 2020, when they evaluated the SARS-CoV-2 outbreak. WHO declined to label the COVID-19 disease a PHEIC, changing their mind just a week later.

And I am sorry, but seriously…. the pronunciation of the emergency status label that was applied to SARS-CoV-2 and now considered for monkeypox is pronounced FAKE??? You can’t make this stuff up…and I didn’t.

The timing of this monkeypox outbreak is especially unfortunate because the enormous numbers of group gatherings to celebrate Pride month bring together “men who have sex with men” in exuberant celebrations, and human nature often takes its course.

Monkeypox is spread by skin-to-skin contact, especially of an intimate nature. WHO reports that the “monkeypox virus is transmitted from one person to another by close contact with lesions, body fluids, respiratory droplets, and contaminated materials such as bedding. The incubation period of monkeypox is usually from 6 to 13 days but can range from 5 to 21 days.”7

Despite the mass gatherings planned around the world to celebrate Pride month, the CDC, NIH, and other public health officials refuse to clearly and broadly state that there should be no intimate contact of any kind between those at risk for this disease or infected during this outbreak.8 Gay and bisexual men need to protect themselves and each other for a few weeks, so they do not get sick. Our friend and colleague, Paul Alexander, Ph.D., has very plainly called out these public officials for their dereliction of duty in failing to warn affected communities clearly about how they can protect themselves and each other.9

In November 2021, a report was issued by the Nuclear Threat Initiative, which, along with the Munich Security Conference, held a tabletop exercise to consider responses to a fictional monkeypox outbreak that was posited to occur in May 2022.10

Stretching credulity, fiction has now been replaced by fact as the world experiences a genuine explosion of the monkeypox disease starting on the exact assigned date. Could this exact prediction be one more big coincidence?

Earlier Prescient Pandemic Predictions

All the way back to 2010 and earlier, there have been tabletop exercises making predictions and running drills on how to handle an emerging pandemic. The pandemic simulation exercise at Johns Hopkins Center for Health Security in November of 2019 predicted an outbreak of a coronavirus.11 Two months later, in January 2020, the first reports of a coronavirus outbreak—Sars-CoV-2—circulated. Now we have had a 2021 tabletop exercise positing an outbreak of monkeypox, predicting an outbreak would occur in May of this year, and here it is, right on schedule.

Lessons from COVID-19

During the early days of COVID, delays in implementing containment measures stretched on for weeks. Hundreds of flights left China daily for the four corners of the earth, carrying infected individuals to many countries, including thousands of returning foreign students to the US. When President Trump suggested that flights from China should be shut down, he was charged with xenophobia.12

Sadly, we failed to learn the lesson of containment and are seeing a repeat with the appearance of monkeypox. Abstinence, the most logical step for containing monkeypox, has not been recommended by the authorities.

CDC, NIH, and other public health authorities fail to take the scientific and medically sound action of advising abstinence and stand by as another plague descends upon the gay community. Instead, there have been multiple official reassurances that monkeypox is not usually contagious and that a vaccine already exists.13

Are we Really this Naïve?

Can we be so naïve as to believe it is chance when two times out of two, there have been practice runs of a mythical epidemic, and then that specific epidemic appears within months? And both times, there are botched efforts to contain the disease when the outbreak is identified, resulting in a worldwide spread of the pathogen. And each time, the pathogen, first Sars-CoV-2 in 2020, and now this strain of monkeypox is unique in its behavior.

Like coronaviruses, viruses related to smallpox, mousepox, monkeypox, cowpox, and others have been the focus of laboratory manipulation and gain of function (GOF) research since at least 2003. Again like coronaviruses, these pathogens are common in the biocontainment labs of the world.14

But…There are Vaccines!

Conveniently, COVID mRNA and DNA vaccines were already in development for some time prior to the SARS-CoV-2 outbreak. And now, as it turns out, we have monkeypox vaccines handy. These vaccines are also used to inoculate against smallpox, which has been eradicated since 1980.15

New York City opened the first clinic for monkeypox vaccines just this week to administer doses. The clinic has already had to cancel further walk-in appointments because, within 24 hours of opening the clinic, they were booked out into the following week.16 The New York City Health Commissioner reports anxiety to be high, especially among sexually active gay and bisexual men, and so the city decided to make the vaccines available.

Cardiac Adverse Events of Special Interest

The two-dose JYNNEOS vaccine administered 28 days apart is a smallpox and monkeypox vaccine.17 The package insert for the JYNNEOS vaccine contains a section on “Cardiac Adverse Events of Special Interest.”18 This raises concern among doctors tracking the alarming number of COVID vaccine cardiac side effects.19 If individuals already have developed cardiac adverse events from COVID vaccines, they need to avoid another vaccine with the same possible adverse effect.

Individuals who have already had a COVID vaccine, and especially anyone who has experienced cardiac complications following a COVID vaccine, need to consider the greater cardiac event risk of a second vaccine exposure when deciding whether to be vaccinated for monkeypox.20 Few hospitalizations and no deaths have been reported for the current outbreak “outside of an endemic country.”21 Business is picking up for the vaccine manufacturer, however.

Mistakes were Made, But No One is Learning

Despite tabletop exercises for COVID and now monkeypox, mistakes are being repeated. Tabletop exercises without emphasis on correcting mistakes make perfect sense only if one is preparing to spread a little plague chaos. The predators have got to have some “practice runs” to ensure everyone is genned in on the complexities of the execution. The propagandists, the social psychologists, the legacy media, the various agencies, the chosen, anointed corporations (Pfizer and Moderna in the case of COVID in the US) …. well, it takes tremendous coordination.

If preventing the spread of disease and helping the sick is the goal, these exercises continue to fail.

What if the goal is vaccines for money and chaos?

Look at what had to happen with COVID in order to achieve the release of the vaccines. Jack up the numbers of COVID deaths by sending infected elders back to nursing homes (NY and NJ, among other states). Suppress successful FDA-approved medications as early treatments like hydroxychloroquine and ivermectin so that the Emergency Use Authorizations could be approved for the vaccines. Manipulate the research to show positive outcomes for vaccines and suppress negative outcomes of the COVID vaccines in trials.22,23 Details of much of the manipulation and the complexities are addressed in our book COVID-19 and the Global Predators: We are the Prey.

I find that using the data we unearthed for our book and continuing to look for the predator connections in chaos further illuminates our current circumstances and removes much of the mystery. The food shortages, energy “shortages,” disruptions in schools, and so many seemingly random actions are explained. Chief among the alarming circumstances are rumors that cash–folding money and coin around the world–will be canceled, and we will all be forced to convert to digital currency and digital wallets. Vaccine passports—in high demand by controlling governments since the COVID pandemic– are one vector being employed to introduce more widely applicable digital wallets. See our column at America Out Loud on why each of us who values freedom must use physical cash instead of digital money, every chance we get.24

There are no Coincidences

This much chaos, this much random disaster in so many sectors, does not just happen. Repeating the same mistakes made in the pandemic that occurred less than three years ago is not just ignorance. We are not just experiencing a streak of bad pandemic luck and massive chaos in other sectors.

There is a huge amount of planning and outright manipulation for so many systems to go so wrong so fast at the same time, both medically and in public health and in other sectors that are being severely disrupted.

What if the deeper purpose of the pandemics is to weaken the nation-states of the world and enable a global-level cabal of private predator corporations, narcissistic billionaires, and the Chinese Communist government to seize world governance.25 A recent and ongoing example of this is the World Health Organization’s attempts to seize enforceable global control of all nations’ health systems and emergency operations when WHO arbitrarily decides it is necessary.26

We cannot afford to be complacent or naïve anymore. Predators exist, and they are stalking us and our democratic republics. Are we going to continue to be their prey until we are too weakened to resist?

Author’s Note: The author wants to acknowledge Gatito Bueno, of the substack “Bad Cattitude” for his article “kitten corner: hey, hey it’s the monkeypox.”27 Gatito Bueno’s substack inspired my initial thoughts and comments on that column and thus this column.

Primary author Ginger R. Breggin. Peter R. Breggin MD and Ginger Breggin are the authors of the bestselling new book, COVID-19 and the Global Predators: We are the Prey, with introductions by top COVID-19 scientists and physicians, Peter A. McCullough MD, MPH; Elizabeth Lee Vliet MD; and Vladimir “Zev” Zelenko MD. Over 100,000 sold.

References:

1 European festivals should not be scrapped due to monkeypox: WHO (yahoo.com)
2 Monkeypox mutates at unprecedented rate, study finds (nypost.com)
3 Phylogenomic characterization and signs of microevolution in the 2022 multi-country outbreak of monkeypox virus | Nature Medicine
4 Pandemic or Epidemic: WHO Monkeypox Announcement Set for Today (newsweek.com)
5 WHO Monkeypox Meeting: What Is an Emergency of International Concern? (newsweek.com)
6 How Serious is Monkeypox? WHO Says Not Global Emergency – Bloomberg
7 Multi-country monkeypox outbreak in non-endemic countries (who.int)
8 Monkeypox | Poxvirus | CDC
9 WARNING: CDC & public health officials & WHO must stop the pandering to the gay community & state just facts, where the risk is, how the risk happens & how to stop it; NOT side step & ENCOURAGE it (substack.com)
10 Strengthening Global Systems to Prevent and Respond to High-Consequence Biological Threats (nti.org)
11 Pandemic simulation exercise spotlights massive preparedness gap | Hub (jhu.edu)
12 After attacking Trump’s coronavirus-related China travel ban as xenophobic, Dems and media have changed tune | Fox News
13 You can be worried about monkeypox if you want to – Vox
14 US develops lethal new viruses | New Scientist
15 Smallpox Questions and Answers: The Disease and the Vaccine (ny.gov)
16 NYC Monkeypox Cases Jump 30% Amid Rush on Limited Vaccine Supply (msn.com)
17 Use of JYNNEOS (Smallpox and Monkeypox Vaccine, Live, Nonreplicating) for Preexposure Vaccination of Persons at Risk for Occupational Exposure to Orthopoxviruses: Recommendations of the Advisory Committee on Immunization Practices — United States, 2022 | MMWR (cdc.gov)
18 Package Insert – JYNNEOS (fda.gov)
19 In memory of those who “died suddenly” in the United States and worldwide, June 14-June 20 (substack.com)
20 Cardiac complications following mRNA COVID-19 vaccines: A systematic review of case reports and case series – PubMed (nih.gov)
21 Global monkeypox outbreak isn’t an international public health emergency ‘at present,’ WHO rules | Fortune
22 WARNING! Pfizer Lied About Results in COVID-19 Vaccine Trials for Babies and Toddlers – Vaccine Impact
23 Serious Adverse Events of Special Interest Following mRNA Vaccination in Randomized Trials by Joseph Fraiman, Juan Erviti, Mark Jones, Sander Greenland, Patrick Whelan, Robert M. Kaplan, Peter Doshi :: SSRN
24 https://www.americaoutloud.com/rescu...gital-slavery/
25 The Inhumanity and Treachery of Governments – Lessons of COVID – America Out Loud
26 Freedom Fighters Stop Dictatorship of World Health Organization – America Out Loud
27 kitten corner: hey, hey it’s the monkeypox (substack.com)

Peter Breggin MD and Ginger Ross Breggin
Peter Breggin MD and Ginger Ross Breggin

Peter Breggin MD and Ginger Ross Breggin have been married and working together for almost 40 years. Peter is known as "The Conscience of Psychiatry" for his many decades of successful reform work in mental health. He has published more than 20 medical and popular books, several coedited or coauthored by Ginger, including the huge bestseller Talking Back to Prozac. He has written more than 70 peer-reviewed publications and testified in court more than 100 times with many cases related to drug company and medical malfeasance. The couple has now turned their attention to the misuse of science and the suppression of freedoms surrounding COVID-19 and its origins by those they identify as "global predators."

Peter and Ginger have written the bestselling new book, COVID-19 and the Global Predators: We are the Prey with introductions by top COVID-19 scientists and physicians, Peter A. McCullough MD, MPH; Elizabeth Lee Vliet MD; and Vladimir "Zev" Zelenko. The book is available everywhere.

CDC Investigates Rare Disease in Florida Dubbed as ‘One of the Worst Outbreaks Among Gay and Bisexual Men in U.S. History’

The U.S. Centers for Disease Control and Prevention (CDC) announced on Wednesday that the agency continued collaborating with the Florida Department of Health to investigate a rare disease outbreak among gay and bisexual men.
In a press release, the CDC said they are assisting with the meningococcal disease outbreak investigation in Florida that spread among homosexual males, including those with HIV.
According to the agency, this is one of the worst outbreaks of meningococcal disease among gay and bisexual men in U.S. history.
CDC is now urging homosexuals to get a MenACWY vaccine if they reside in Florida or by contacting their doctor’s office, pharmacy, community health center, or local health department or their healthcare provider about the vaccination if traveling to Florida.

Population control = the end game

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Jikkyleaks (Fan account) 🐭
@Jikkyleaks
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20h
This is a massive safety signal for infertility. Germany's FIRST report of birth rates since the rollout.

Remember that the birth rate data is 9 months too late.

If the next quarter is worse, this is Children of Men scenario.
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Jikkyleaks (Fan account) 🐭
@Jikkyleaks

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20h
For the years 2011-2021 the average number of births is 63,911 for the Jan-Mar quarter, with a standard deviation of 1015

The drop to 54871 for 2022 is approx 9 SD.

9 Sigma. Unicorn events.

The money people understand this.

@chrismartenson

https://seekingalpha.com/instablog/5...unicorn-events
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Jikkyleaks (Fan account) 🐭
@Jikkyleaks
For a 9 sigma drop in birth rates to have happened in Jan-Mar 2022, something dramatic had to have happened to stop pregnancies occurring in March to June 2021.

I wonder what that could be?
Were couples depressed? Looking to move house? Too busy?

https://duckduckgo.com/?q=fertility+n

https://ecp.yusercontent.com/mail?ur...V6TV0M7Hrg--~D



BREAKING: HEARING ON MOTION TO DISMISS AT 8:30 A.M. CENTRAL TOMORROW MORNING IN SALIER V. WALMART!

As most of you know, last Fall we announced that, thanks to the generous support of our donors, we were funding the case of retired U.S. Marine Bill Salier against Walmart and Hy-Vee Supermarkets in Minnesota. Bill and his wife Karla were critically ill with covid in October 2021 when their physician, Dr. Molly James, prescribed them ivermectin. When Bill and Karla tried to pick up the prescription at Walmart, however, the pharmacist refused to fill it. When Dr. James called the pharmacist and asked him to do his job, he hung up on her. Bill and Karla tried to get the prescription filled at Hy-Vee, but were met with similar obstinance from a pharmacist there. Finally, they resorted to eating horse paste to get the life-saving ivermectin. Within 24 hours, the Saliers noticed significant improvement, and within a week, both had almost fully recovered.


WE WILL NOT ALLOW THIS ABUSE TO STAND. In January, the Saliers' case was filed in federal court. Predictably, both Walmart and Hy-Vee filed motions to dismiss, to which the Saliers' attorneys have objected. The motion will be heard tomorrow at 8:30 a.m. Central Time at the federal courthouse in Minneapolis, Minnesota. Unfortunately, the hearing will not be livestreamed, but the public may attend in person. We strongly encourage anyone within driving distance who is available tomorrow to attend to show support for the Saliers and for medical freedom!


Without the generous support of our donors, we would not have been able to even take up this fight. We have so many more cases waiting in the wings, but unfortunately funding has slowed due to the economic downturn.

https://www.youtube.com/watch?v=YyWclWGpnMQ


https://www.youtube.com/watch?v=YyWclWGpnMQ




https://i.ytimg.com/an_webp/YyWclWGp...huzOf5pPkZ6puQ

Nigel Farage: This is no longer about health

375,586 views
Jun 16, 2022

Fox News


Former Brexit Party leader Nigel Farage joined 'Fox & Friends First' to discuss Novak Djokovic being banned from the U.S. Open over his vaccination status. #foxnews

Biden’s Betrayal of Military: Part II~Threat to Military Readiness

Dr. Vliet interviews guests Lt. General Rod Bishop, Jr., Lt. Billy Moseley, and Attorney Mike Rose add to the voices from part one of this series to speak out about the Biden Administration and Biden-appointed Department of Defense (DoD) Lloyd Austin continuing to undermine military readiness and combat effectiveness with the unlawful order mandating the EUA experimental COVID shot. https://www.americaoutloud.com/bidens-betrayal-of-our-military-the-threat-to-military-readiness/

Biden’s Betrayal of Military: Part I~Threat to National Security

Dr. Vliet interviews guests General Tom McInerney, Lt. Col. Peter C. Chambers, D.O., and Lt. John Bowes, speak out about the Biden Administration’s using COVID to engineer a systematic destruction of America’s military and national security. It’s being executed through a purging of the most experienced and well-trained personnel and replacing them with “woke” indoctrinated extreme leftists who place ideology before God, Corps, Duty, Honor, and Country. This alarming betrayal of our national defense has prompted Dr. Vliet and Truth for Health Foundation, and the Foundation’s Military Advisory Council to sound the alarm for the public to understand the dire threat to all of us and America’s national security with the damage being done in designed destruction of our military readiness and fitness. As a result of Biden’s attack on the military, there have been deaths, injuries, and medical damage/disability from the shots, plus service members being forced out of the military, many without due process, causing dire consequences to America. https://www.americaoutloud.com/biden...onal-security/

New VAERS Data as of June 17, 2022 (posted June 24, 2022)

31,556 Total Deaths and 1,397,524 Total Adverse Events

29,031 Pfizer/Moderna and 2,525 J&J Deaths

1,307,928 Pfizer / Moderna and 89,596 J&J Adverse Event

Source: https://drtenpenny.com/newsletter/

Dachsie Comment:

The failure of Dr Malone's mRNA technology has been a monumental learning experience for science and for the world. Measurement of the cost of this learning all depends on your value system. It brought abundant filthy lucre to some and brought death and permanent disability to millions. This learning experience was highly successful toward installing a One World Death and Slavery System for All.
_______________________

https://www.youtube.com/watch?v=9E2UkhCWosg

https://www.youtube.com/watch?v=9E2UkhCWosg

54:42 video runtime

Dr. Robert Malone, Inventor of mRNA technology discusses the Spike Protein | Interview

1,147,016 views
Jul 8, 2021


TrialSite News


Join The Conversation! | https://trialsitenews.com/

Dr. Robert Malone, Inventor of mRNA technology discusses the Spike Protein.


Dr. Erin Stair discusses with Dr. Robert Malone about the COVID-19 Spike Protein vs the Spike Protein produced by the COVID-19 Vaccines and more.


Referenced Articles:
Salk Institute Paper | https://www.salk.edu/news-release/the...
Canadian physicians FOIA | https://trialsitenews.com/did-pfizer-...
Reuters Fact Check | https://www.reuters.com/article/factc...
Circulating SARS-CoV-2 Vaccine Antigen Detected in the Plasma of mRNA-1273 Vaccine Recipients | https://academic.oup.com/cid/advance-...

Dachsie comment:

Dr. Levine is probably going to be Dr. Fauci's replacement so is relevant to Coronavirus topic.
______________________

https://blog.nomorefakenews.com/2022...ir-gender-war/

Medical dictatorship: their gender war
June 27, 2022

by Jon Rappoport

June 27, 2022

For my article on the Supreme Court’s ruling overturning “Roe v Wade” — “Abortion: the Democrats’ Gold Rush” — click here.

I have a two-sentence introduction before we get to the guts of this story:

Whenever a typical “liberal” college educated parent hears a doctor or medical bureaucrat utter a pronouncement, the parent, like a doomed trained monkey, AUTOMATICALLY replies, “Well, this evidence certainly has some merit…”

God help the child who has such a parent.

Gateway Pundit has the story. Here are quotes; then I’ll have comments.

“Joe Biden’s transgender Assistant Health Secretary Dr. Rachel (Richard) Levine spoke at a DNC pride month event on Friday.”

“On Friday, Dr. Levine said sex reassignment surgery (castration) and puberty blockers (chemical castration) for KIDS is ‘lifesaving, medically necessary, age appropriate, and a critical tool’.”

“Levine recently said that there is no debate about ‘gender-affirming’ care for kids.”

“’There is no argument among medical professionals — pediatricians, pediatric endocrinologists, adolescent medicine physicians, adolescent psychiatrists, psychologists, etc. — about the value and the importance of gender-affirming care,’ Levine said.”

“According to the American College of Pediatricians, no single long-term study demonstrates the safety or efficacy of puberty blockers, cross-sex hormones, and surgeries for transgender-believing youth.”

“Puberty blockers may cause depression and other emotional disturbances related to suicide. The package insert for Lupron, the number one prescribed puberty blocker in America, lists ‘emotional instability’ as a side effect and warns prescribers to ‘Monitor for development or worsening of psychiatric symptoms during treatment’.”

OK. The big takeaway from these statements is: we’re supposed to believe we’re talking about a MEDICAL condition and MEDICAL TREATMENT.

Once that bell is rung, all bets are off. “Well, the doctor says Jimmy has gender dysphoria, a medical/psychiatric condition, and his desire to transition to a girl needs treatment. The treatment allows him to make the transition.”

As with other issues, the word from on high is, the science is settled.

Forget the fact that the American College of Pediatricians disagrees. Ultimately, what is and isn’t science is decided at a political level.

Forget the fact that gender dysphoria has no defining physical diagnostic test. No blood test, no urine test, no hair test, no genetic assay, no brain scan. Its existence as a condition is backed by zero evidence.

Forget the fact that the treatments are toxic and destructive.

The medical/political colossus has spoken. Doubters are now referred to “the science.”

This is how medical dictatorship operates. You might recall that’s how it operated with a little thing called COVID.

Dr. Rachel Levine is trying out for the role of Anthony Fauci.

Civilians everywhere want to argue against children undergoing transition to another gender, but the authorities want to head that off at the pass by claiming “it’s all medical and we have the knowledge and you don’t know anything. Case closed.”

If parents huddle in the dark, afraid of a scornful look from a doctor or a medical bureaucrat, the war is over. It’s lost. The war against children will be scorched earth and scorched lives.

I can hear that college educated parent I referred to saying, “Well, to be reasonable, there is some merit to the argument that certain young children have a need to transition, and we have to discern these cases carefully and consider the medical evidence…”

This is what all losers say just before the enemy pours tons of gasoline on the fire and the city burns down.

Dachsie comment:

In the USA what is and is not science, medicine, healthcare, religion, law, crime, government, rights, and jurisprudence is decided at a political level.

https://live.childrenshealthdefense....chd/2gSk68c9FD

embedded video

1:12

June 27, 2022
Good Morning CHD
‘Good Morning CHD’ Episode 61: FDA’s Future Framework With Dr. Paul Alexander + STOPPING Quarantine Facilities in NY

https://live.childrenshealthdefense....chd/2gSk68c9FD


While the executive branches seek “unfettered power” to quarantine and mandate, controlling the bodies and lives of Americans, Pfizer and Moderna shots continue to wreak havoc on children. On today’s “Good Morning CHD,” guests attorney Bobbie Anne Cox and Paul Alexander, Ph.D., discuss critical events and efforts being made to further exacerbate tyrannical power. Also, viewers hear ways that they can participate in the fight for medical freedom.

Save Baby August, Action Alert: https://alignact.com/go/save-baby-august-

Please act to help this precious baby.

https://alignact.com/sites/default/f...&itok=c0cKv-Of

BREAKING INTERVIEW: Six-month-old Denied Life-Saving Heart Transplant Due to Vaccination Status: https://live.childrenshealthdefense....nts/wu-mqNMqz-

URGENT! Tell the FDA — Vote NO on ‘Future Framework’: https://childrenshealthdefense.org/c...ure-framework/

Attorney Bobbie Anne Flower-Cox, Website: http://www.coxlawyers.com/

Uniting NYS Lawsuit: https://unitingnys.com/lawsuit

Dr. Paul Alexander, Website: https://www.drpaulalexander.com/

Dr. Paul Alexander, Substack: https://paulalexander.substack.com/

I learned about this illegal unconstitutional scheme on this show...

Horrible totalitarian sneaking around the rule of law to quarantine and grap people out of their homes and taken to quarantine facilities.

https://live.childrenshealthdefense....chd/2gSk68c9FD

https://unitingnys.com/lawsuit/

The governor of New York state and a state agency is making law now and they are calling it a "regulation."
If NY state is allowed to sneak this through it is all over for all over the country.

The Regulation…
10 NYCRR 2.13 “Isolation and Quarantine Procedures”

Allows the DOH to pick and choose who they want to force to isolate or quarantine, without proof that the person poses a health threat, for however long the DOH wishes to force the quarantine, and at a location that the DOH deems appropriate (which can include a quarantine “facility” or detention center).
They do not need to prove that you are actually sick. They can just suspect that you MIGHT be harboring a communicable disease.
There is no age restriction, so they can force you, or your child, or your elderly parent/grandparent into isolation or quarantine, for however long they want!
It is the antithesis of what our country stands for, so we intend to stop them!

You can read the full text of the regulation here: https://regs.health.ny.gov/volume-title-10/content/section-213-isolation-and-quarantine-procedures

Title: Section 2.13 Isolation and Quarantine Procedures
Effective Date
04/22/2022

2.13 Isolation and Quarantine Procedures

(a) Duty to issue isolation and quarantine orders

(1) Whenever appropriate to control the spread of a highly contagious communicable disease, the State Commissioner of Health may issue and/or may direct the local health authority to issue isolation and/or quarantine orders, consistent with due process of law, to all such persons as the State Commissioner of Health shall determine appropriate.

(2) Paragraph (1) of this subdivision shall not be construed as relieving the authority and duty of local health authorities to issue isolation and quarantine orders to control the spread of a highly contagious communicable disease, consistent with due process of law, in the absence of such direction from the State Commissioner of Health.

(3) For the purposes of isolation orders, isolation locations may include home isolation or such other residential or temporary housing location that the public health authority issuing the order determines appropriate, where symptoms or conditions indicate that medical care in a general hospital is not expected to be required, and consistent with any direction that the State Commissioner of Health may issue. Where symptoms or conditions indicate that medical care in a general hospital is expected to be required, the isolation location shall be a general hospital.

(4) For the purposes of quarantine orders, quarantine locations may include home quarantine, other residential or temporary housing quarantine, or quarantine at such other locations as the public health authority issuing the order deems appropriate, consistent with any direction that the State Commissioner of Health may issue.

(b) Any isolation or quarantine order shall specify:

(1) The basis for the order;

(2) The location where the person shall remain in isolation or quarantine, unless travel is authorized by the State or local health authority, such as for medical care;

(3) The duration of the order;

(4) Instructions for traveling to the isolation or quarantine location, if appropriate;

(5) Instructions for maintaining appropriate distance and taking such other actions as to prevent transmission to other persons living or working at the isolation or quarantine location, consistent with any direction that the State Commissioner of Health may issue;

(6) If the location of isolation or quarantine is not in a general hospital, instructions for contacting the State and/or local health authority to report the subject person’s health condition, consistent with any direction that the State Commissioner of Health may issue;

(7) If the location of isolation or quarantine is a multiple dwelling structure, that the person shall remain in their specific dwelling and in no instance come within 6 feet of any other person, and consistent with any direction that the State Commissioner of Health may issue;

(8) If the location of isolation or quarantine is a detached structure, that the person may go outside while remaining on the premise, but shall not leave the premise or come within 6 feet of any person who does not reside at the premise, or such other distance as may be appropriate for the specific disease, and consistent with any direction that the State Commissioner of Health may issue;

(9) Such other limitations on interactions with other persons as are appropriate, consistent with any direction that the State Commissioner of Health may issue;

(10) Notification of the right to request that the public health authority issuing the order inform a reasonable number of persons of the conditions of the isolation or quarantine order;

(11) A statement that the person has the right to seek judicial review of the order;

(12) A statement that the person has the right to legal counsel, and that if the person is unable to afford legal counsel, counsel will be appointed upon request.

(c) Whenever a person is subject to an isolation or quarantine order, the State Department of Health or local health authority, or the local health authority at the State Department of Health’s direction shall, consistent with any direction issued by the State Commissioner of Health:

(1) monitor such person to ensure compliance with the order and determine whether such person requires a higher level of medical care;

(2) whenever appropriate, coordinate with local law enforcement to ensure that such person comply with the order; and

(3) the extent such items and services are not available to such person, provide or arrange for the provision of appropriate supports, supplies and services, including, but not limited to: food, laundry, medical care, and medications.

(d) If the location of an isolation or quarantine order is owned by a landlord, hotel, motel or other person or entity, no such landlord or person associated with such hotel, motel or other person or entity shall enter the isolation or quarantine location without permission of the local health authority, and consistent with any direction that the State Commissioner of Health may issue.

(e) No article that is likely to be contaminated with infective material may be removed from a premise where a person is isolated or quarantined unless the local health authority determines that such article has been properly disinfected or protected from spreading infection, or unless the quarantine period expires and there is no risk of contamination. Such determinations shall be made pursuant to any direction that the State Commissioner of Health may issue.

(f) Any person who violates a public health order shall be subject to all civil and criminal penalties as provided for by law. For purposes of civil penalties, each day that the order is violated shall constitute a separate violation of this Part.

(g) Duty of attending physician

(1) Every attending physician shall immediately, upon discovering a case or suspected case of a highly contagious reportable communicable disease, cause the patient to be appropriately isolated and contact the State Department of Health and the local health authority where the patient is isolated and, if different, the local health authority where the patient resides.

(2) Such physician shall advise other members of the household regarding precautions to be taken to prevent further spread of the disease, consistent with any direction that the State Commissioner of Health may issue.

(3) Such physician shall furnish the patient, or caregiver of such patient where applicable, with detailed instructions regarding the disinfection and disposal of any contaminated articles, consistent with any direction that the State Commissioner of Health may issue.


Statutory Authority
Public Health Law, Sections 225, 576, and 2803
Volume

VOLUME A (Title 10)

https://childrenshealthdefense.org/defender/who-fda-gates-future-framework-covid-vaccines/?utm_source=salsa&eType=EmailBlastContent&eId=090a 5127-70f9-4314-aabb-346577f48bc9


06/27/22
•

COVID › Views
[SIZE=4]Breaking: WHO Behind FDA Scheme to Skip All Future Clinical Trials for COVID Vaccines[/SIZE]

The “Future Framework” is coming from the World Health Organization, and the Bill & Melinda Gates Foundation is the biggest voluntary contributor to the WHO, so Gates is likely directing the play.
By
Toby Rogers, Ph.D.

https://childrenshealthdefense.org/w...re-800x417.jpg

Editor’s note: The U.S. Food and Drug Administration (FDA) tomorrow, June 28, will vote on the “Future Framework,” a scheme that would allow Pfizer and Moderna to “reformulate” COVID-19 mRNA vaccines in perpetuity, without conducting clinical trials on the new vaccines. Click here to tell the FDA to vote no on the “Future Framework.”

Breaking: WHO Behind FDA Scheme to Skip All Future Clinical Trials for COVID Vaccines


Late Friday afternoon, the FDA released its agenda for the Vaccines and Related Biological Products Advisory Committee (VRBPAC) meeting that will vote on the Orwellian “Future Framework” on Tuesday, June 28.

Then on Saturday morning, the FDA released a briefing document in connection with this scheme to end science as we know it in connection with future COVID-19 shots. (Much appreciation to the brilliant James Roguski for alerting me to these documents.)

In this article, I will explain what is in the briefing document, what is likely to happen at the meeting and what can be done about it.

The FDA’s ‘Future Framework’ briefing document

The briefing document is 18 pages of text, 1.5 line spacing, with just 19 references — 9 of which are pre-prints or from the CDC’s in-house newsletter Morbidity and Mortality Weekly Report (MMWR) which means they are not peer-reviewed.

Any true believer in The Narrative(TM) could have written this in a few hours. To base the entire future of COVID-19 shots on this glorified undergrad term paper is madness.

As I predicted, even though the April 6 meeting was presented as an exploratory initial conversation that reached no conclusions whatsoever, the “Future Framework” is now being presented by the FDA as a done deal, fait accompli, you’d have to be crazy to insist on proper safety studies.

The core argument of the briefing document is hilarious (or rather, it would be hilarious if it was not a plan to permanently institutional genocide and hide the evidence). In several places the FDA argues (colloquialisms mine):

1. These COVID-19 shots work great, miracles really, incredibly effective, boy howdy do they work well! Boosters too, total home run, the Israelis even have 10-weeks of data showing that they might help old people. What more evidence could you want?

2. Okay, well, it depends on what you mean by work. These shots do not stop infection, transmission, hospitalization, or death, even though that’s why we licensed them. Any protection wears off fairly quickly, but It’s Not Our Fault(TM) because This Wily Virus(TM) mutates too fast and no one told us that it would ever mutate.

3. So these shots must be reformulated but we cannot possibly ask Lord Pharma to do proper clinical trials ever again because we already know that these shots work great (see point #1)!

The briefing document literally states:

“The evaluation of modified vaccines for the purpose of vaccine strain composition decisions will need to rely mainly on comparative immunogenicity data due to the time constraints involved in vaccine manufacturing and clinical efficacy evaluation.”

Did you catch that? The evaluation “will need to rely on” (no decision to be made here) measures other than actual health outcomes because of “time constraints.”

Ah, $cience!

Moderna, Pfizer and Novavax are all developing reformulated COVID-19 shots. But they know that the FDA is not going to look at health outcomes so they are going to great lengths to jack up the antibody response.

Pfizer tested a double-strength dose (60 mcg of mRNA instead of 30 mcg) even though they had previously ruled out a higher dose because of safety concerns. So the antibody levels are through the roof.

But the VRBPAC admitted on April 6 that there are no known correlates of protection (meaning: antibody levels do not tell you who will be immune) so these antibody measures are medically meaningless.

Sane people realize that if you turbo charge the immune response, you may also turbo charge adverse events. But the “Future Framework” allows pharmaceutical companies to skip clinical trials altogether.

Furthermore, all of these companies are developing shots to target the original Omicron strain (BA.1) even though it has already been supplanted by other variants (BA.4 and BA.5).

The FDA and these companies claim that shots targeting BA.1 will be effective against later variants but I do not know how they can possibly argue that given the total absence of actual health data.

Words that you will NOT find in the FDA “Future Framework” briefing document:

original antigenic sin,
antibody-dependent enhancement,
prion disease,
myocarditis,
VAERS
adverse events, or
side effects.

So the FDA is literally not looking out for any of the worst-case scenario possibilities.

The “Future Framework” is a plan to base the entire COVID-19 vaccine program on magical thinking rather than science.

What’s likely to happen at the VRBPAC meeting on Tuesday, June 28

The cartel is predictable because they follow a playbook and they use the same cast of characters over and over again.

The first presentation will be by CDC staffer Heather Scobie. She will likely take her slides from the June 7 VRBPAC meeting, change the date on the first slide and update them a bit to show that Omicron has become the predominant SARS-CoV-2 variant in the U.S.

The gist will be that there is no point in vaccinating against the “prototype” Wuhan lab leak variant, nor Alpha, Beta, Delta or Gamma, because it’s all Omicron right now.

What she will NOT tell you is that Moderna and Pfizer are designing shots to target the BA.1 version of Omicron and now that variant is waning and being replaced by BA.4 and BA.5. Furthermore, she will not mention the fact that these shots are fueling the evolution of variants that evade any protection from vaccines.

Dr. Scobie will be followed by another CDC staffer, Ruth Link-Gelles who will likely dust off one of her slide decks from the four VRBPAC and four ACIP meetings that have already happened this month and discuss COVID-19 vaccine effectiveness in adults. RLG cracks me up because she absolutely does not give a damn.

She shows slide after slide of negative efficacy from these worthless shots and she does not care because she knows that the VRBPAC will approve anything that has the word vaccine on the vial. RLG’s presentations are a token attempt to play it straight with the data but then all of her data is instantly memory-holed and never spoken of again.

Then, I’ve got to hand it to the cartel for choosing their next speaker — Justin Lessler, from the University of North Carolina. Dr. Lessler has gotten 10 grants from the Bill & Melinda Gates Foundation in recent years (see pages 26 to 30 of his CV here).

Then he’s gotten another 10 grants from NIH and/or Tony Fauci’s National Institute of Allergy and Infectious Diseases (NIAID).

Given that, what are the odds that Dr. Lessler will criticize The Narrative(TM)? Zero.

Gates and Fauci literally have their guy inside the meeting doing the modeling about how we should think about the future epidemiology of COVID-19.

Gates figured out in 2017 that modeling is the tail that wags the dog of policy and has invested heavily in it ever since.

Dr. Lessler is soaked head to toe in conflicts of interest — he should not be allowed within 100 miles of this committee — and yet the FDA will not even require a conflict waiver from this guy.

Cartel gonna cartel.

After a short break, Stephen Hoge President of Moderna, Dena Swanson, VP of Pfizer, and Greg Glenn, President of Novavax will explain how wonderful their reformulated COVID-19 shots are but they will argue that there is simply no time to conduct proper clinical trials anymore.

None of their data will be peer-reviewed so it will all be fanciful fiction — 95% to 100% efficacy based entirely on belief.

Then the FDA will bring in two closers (and this is where it gets really interesting).

Kanta Subbarao, Director of the World Health Organization (WHO) Collaborating Center in Melbourne, Australia will present “Considerations for Vaccine Strain Composition from the WHO. TAG CO-VAC.”

I did not understand until just yesterday (as I started to write this article) that this entire “Future Framework” is actually coming from the WHO. The Bill & Melinda Gates Foundation is the biggest voluntary contributor to the WHO. so Gates is likely directing the play.

Gates requires that WHO. use the McKinsey consulting firm so this is probably a McKinsey operation (and McKinsey also works for Pharma so this is a huge conflict of interest). As Naomi Wolf points out, the involvement of the WHO. also raises troubling questions about the influence of the Chinese Communist Party over this process.

As far back as January, the WHO/Gates/McKinsey junta realized that these shots were terrible and so they decided to use that as an opportunity to seize even more power and control.

The WHO. set up a Technical Advisory Group on COVID-19 Vaccine Composition (TAG-CO-VAC) to implement these Orwellian “Future Frameworks” across the developed world to lower manufacturing costs for Pharma and avoid bothersome health data that might hurt profits.

All the messaging we have seen from the FDA and leaked to the press was initially developed and released by TAG-CO-VAC.

Before joining the WHO., Kanta Subbarao was at NIAID for 14 years, so she’s a loyal lieutenant for Fauci.

She will polish off her slides from the April 6 VRBPAC meeting to argue that COVID-19 is similar to influenza, that strain selection must be coordinated globally and that multivalent New & Improved(TM) COVID-19 Shots Now with Omicron!(TM) will save the day and end the pandemic.

None of her claims will be true but they are what the cartel wants to be said and this is more like a well-funded hostage video than anything else so that’s what we’re going to get.

Finally, the FDA will bring in Jerry Weir, who looks like a cross between Yosemite Sam and Sam Elliott. He’ll slightly update his slides from April as well and then just go round and round with droll observations about the (failed) flu strain selection process and how it should be a model — until the committee is dizzy and willing to agree to anything.

Officially the question that will be voted on is:

“Does the committee recommend inclusion of a SARS-CoV-2 Omicron component for COVID-19 booster vaccines in the United States?”

This language obscures a lot. Boosters are the market now. By calling them boosters instead of reformulated shots (which is what they actually are), they will not go through new clinical trials.

Over the summer, earlier versions of the shot will quietly be withdrawn from the market and the reformulated shots that skipped clinical trials will become the only option. So this is the FDA’s weasel word way of sliding down the slippery slope into no more clinical trials for COVID-19 shots ever again.

If the FDA stated plainly what they are up to there would be riots.

What is to be done

We only have about 24 hours to act so let’s leave it all on the field!

Please submit a formal comment to the regulations.gov website stating that the FDA must reject the “Future Framework” and that all reformulated COVID-19 shots must go through proper human clinical trials. The docket number is FDA-2022-N-0905.

The docket will close Monday night June 27 at 11:59 Eastern time. Click here to go to the relevant page on the regulations.gov website and look for the blue comment button in the upper left-hand corner.

The FDA lies about the number of comments submitted but we have a lawsuit going about that so the more comments we can submit (that they will subsequently hide) the better for our case.

In addition, below are the email addresses of everyone at the FDA/VRBPAC who has a say in this matter. It is our right to share with them our thoughts and concerns about this process. You can share your own story or copy and paste the message below.

Subject line: All reformulated COVID-19 shots MUST go through proper clinical trials

The safety and efficacy of all reformulated COVID-19 shots must be evaluated through:

Large (50,000+ person) double-blind randomized controlled trials with inert saline placebos conducted by an independent third party.
The treatment and control groups must be followed for life to monitor adverse events and all-cause mortality (no more wiping out the control group after 6 months to hide bad outcomes).
We also demand greater than 90% efficacy against infection with less than 0.1% Grade 3 or higher adverse events; proper monitoring for carcinogenesis, mutagenesis and impairment of fertility; and immediate release to the public of all clinical trial documents submitted to the FDA.

sean.mccluskie@hhs.gov, commissioner@fda.hhs.gov, DeanofPublicHealth@brown.edu, Aux7@cdc.gov, Peter.Marks@fda.hhs.gov, Hong.Yang@fda.hhs.gov, Richard.Forshee@fda.hhs.gov, Huilee.Wong@fda.hhs.gov, Leslie.Ball@fda.hhs.gov, Doran.Fink@fda.hhs.gov, jerry.weir@fda.hhs.gov, hanae@bcm.edu, paula.annunziato@merck.com, adam.berger@nih.gov, hbernstein@northwell.edu, acohn@cdc.gov, anc0@cdc.gov, hjanes@fredhutch.org, hgans@stanford.edu, david.kim@hhs.gov, asmonto@umich.edu, offit@chop.edu, spergam@fredhutch.org, Jportnoy@cmh.edu, erubin@hsph.harvard.edu, erubin@nejm.org, ashane@emory.edu, swamy002@mc.duke.edu, fullerao@umich.edu, RandyHawkins@cdrewu.edu, officeofthepresident@mmc.edu, JYLee@uams.edu, ofer.levy@childrens.harvard.edu, wayne_marasco@dfci.harvard.edu, cmeissner@tuftsmedicalcenter.org, mrn8d@virginia.edu, stanley-perlman@uiowa.edu, mhsawyer@ucsd.edu, mew2@cdc.gov, jlessler@unc.edu

Originally published by Toby Rogers on his Substack page, uTobian.

The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children's Health Defense.

https://childrenshealthdefense.org/d...b-346577f48bc9


06/27/22

COVID News Watch
CDC Confirmed Post-Vaccination Death From Blood Clotting Two Weeks Before Alerting Public + More

The Defender’s COVID NewsWatch provides a roundup of the latest headlines related to the SARS CoV-2 virus, including its origins and COVID vaccines.
By
The Defender Staff

CDC Confirmed Post-Vaccination Death From Blood Clotting Two Weeks Before Alerting Public: Emails

The Epoch Times reported:

The Centers for Disease Control and Prevention (CDC) confirmed in late 2021 that a person died from blood clotting after receiving a COVID-19 vaccine that had been linked with an increased risk of blood clotting, but did not alert the public for two weeks, newly obtained emails show.

Dr. Tom Shimabukuro, a CDC official, told colleagues at the CDC and the Food and Drug Administration (FDA) on Dec. 2, 2021, “We have confirmed a 9th thrombosis with thrombocytopenia syndrome (TTS) death following Janssen vaccination,” according to emails obtained by The Epoch Times through a Freedom of Information Act request.

Officials had recommended a nationwide pause on the administration of the vaccine, produced by Johnson & Johnson (J&J) subsidiary Janssen, in April 2021 after six women experienced TTS after J&J vaccination and three died. But they lifted the pause after determining the vaccine remained safe and effective.
Young Men’s Myocarditis Risk 5 Times Higher With Moderna vs Pfizer Vax — but Canadian Study Finds That 8-Week Interval Before Second Dose Attenuates Some of the Risk

MedPage Today reported:

The risk of heart inflammation following the second dose of an mRNA COVID-19 vaccine was substantially higher in younger men with Moderna‘s product (Spikevax) versus Pfizer/BioNTech’s (Comirnaty), though some of this risk was reduced with longer spacing between doses, a population-based study from Canada found.

Cases of myocarditis or pericarditis were highest in men ages 18-24, reaching 299.5 cases per million-second doses of Moderna’s vaccine (95% CI 171.2-486.4), as compared to 59.2 cases per million-second doses of Pfizer’s vaccine (95% CI 19.2-138.1), reported Sarah Buchan, Ph.D., of Public Health Ontario in Toronto, and colleagues in JAMA Network Open.

In this group of men, an 8-week interval or longer lowered the second-dose risk, but it was still markedly higher with Moderna’s product:

Data on boys ages 12-17 years were only available with Pfizer’s product (Moderna’s vaccine was not authorized in Canada for this age group during the study period), and this group saw an even higher rate of myocarditis following the second dose (97.3 cases per million, 95% CI 60.3-148.8) than older males who received Pfizer’s vaccine.
NYC Lawmaker Slams ‘Outrageous’ Lack of Monkeypox Vaccine

New York Daily News reported:

The state is being urged to boost supplies of monkeypox vaccine after all the city’s vaccination appointments were quickly booked last week.

State Sen. Brad Hoylman is calling on Gov. Hochul and Health Commissioner Mary Bassett to get extra doses from the U.S. Centers for Disease Control and Prevention (CDC) as soon as possible.

“We desperately need additional monkeypox vaccines,” the Manhattan Democrat told the Daily News on Sunday. “It’s an outrage that New York City received 1,000 vaccines for an LGBTQ population that is greater than 700,000 people.”

More than 3,300 cases have been found in the U.S., according to the CDC, with 39 of them in the Big Apple, the city Health Department found. Monkeypox has a low fatality rate in Africa and no deaths have been reported in the new outbreak.
COVID Vaccines for Infants Arrive in Florida. Here’s Why Doctors Are Throwing Them Away

Miami Herald reported:

Dozens of South Florida pharmacies, community health centers, children’s hospitals and pediatricians received delivery this week of the first COVID-19 vaccines available for children as young as 6 months old — much earlier than anticipated after state officials missed a deadline for pre-ordering the shots.

But pediatricians and public health advocates working to vaccinate newly eligible children under 5 said they are throwing away the majority of the doses they have ordered because Gov. Ron DeSantis will not authorize state programs to administer the vaccines for infants and toddlers, effectively cutting off supply to many family doctors. The health department also will not promote the vaccines to parents, some of whom are hesitant to have their young children vaccinated.

Parents have mixed feelings about the vaccines. Some are actively seeking it for their children under 5, the last group to be authorized for the COVID vaccines. Others are holding back, concerned about whether there has been enough research on the vaccines and their impact on young children.

As a result, initial demand has been low, and doctors are throwing away vaccines. That’s because each vaccine vial contains 10 doses, and once a vial is opened, it has to be used within 12 hours.

1 Million Copies Sold — ‘The Real Anthony Fauci’ — BUY TODAY!

U.S. Grapples With Whether to Modify COVID Vaccine for Fall

Associated Press reported:

U.S. health authorities are facing a critical decision: whether to offer new COVID-19 booster shots this fall that are modified to better match recent changes in the shape-shifting coronavirus.

Moderna and Pfizer have tested updated shots against the super-contagious Omicron variant, and advisers to the Food and Drug Administration will debate Tuesday if it’s time to make a switch — setting the stage for similar moves by other countries.

In an analysis prepared for Tuesday’s meeting, FDA officials acknowledged targeting last winter’s version of Omicron is “somewhat outdated” since it already has been replaced by its even more contagious relatives.
Pfizer Says Its Omicron-Containing Boosters Outperform Current Vaccine

STAT News reported:

Pfizer said Saturday that using new versions of its COVID-19 vaccine as boosters led to a superior antibody response against the Omicron variant compared to its current shot.

The results in some ways mirror those released by Moderna earlier this month. Data from both companies will be evaluated on Tuesday by a panel of experts convened by the Food and Drug Administration in the hopes of deciding what strains of the SARS-Cov-2 virus should be included in booster shots for the fall. Companies will need lead time to manufacture doses of new vaccines if it is decided they are needed.

The Pfizer data introduce a new question for the FDA panel to consider. Moderna released data from only a bivalent vaccine, meaning that the vaccine contains antigens for both the Omicron variant and the original strain that was prevalent earlier in the pandemic. Pfizer and its partner BioNTech provided data for both the bivalent vaccine and a monovalent one, which contained only antigen for the Omicron variant.
New Hampshire Gov. Chris Sununu Vetoes Bill to Dispense Ivermectin by Standing Order

CBS News Boston reported:

Republican Gov. Chris Sununu on Friday vetoed a bill that would have permitted pharmacists to dispense a parasite drug to treat COVID-19 by means of a standing order without a prescription.

Sununu said in a news release that New Hampshire currently only has four instances in which pharmacists can dispense medication without a prescription: smoking cessation, contraception, substance use disorder and treatment for sexual assault.

He said all of them “have gone through rigorous reviews and vetting to ensure they meet all the necessary protocols prior to a medication being dispensed via standing order.”

He also said ivermectin remains available for individuals if prescribed by their doctor.
Experts Expect Subvariants to Cause ‘Substantial’ Summer Cases of COVID

The Boston Globe via MSN reported:

Until last week, Dr. Ali Mokdad expected the United States to have “a very good summer” in terms of COVID-19. Projections by the Institute for Health Metrics and Evaluation, where he works, forecasted falling cases, hospitalizations and deaths through at least September.

Then, circumstances changed: Researchers discovered that BA.4 and BA.5 — subvariants of Omicron spreading in the United States — are “immune escapes,” adept at avoiding the antibodies the body produces after vaccination or infection to neutralize the virus.

“That has changed our view of what will happen this summer,” Mokdad said. Though he still expects cases to decrease, the decline will be slower and smaller than projected.
WHO: Monkeypox Outbreak Not yet a Global Public Health Emergency

STAT News reported:

The World Health Organization on Saturday declined to declare the unprecedented monkeypox outbreak that has spread around the world a public health emergency as of now.

A public health emergency of international concern, or PHEIC, grants the WHO director-general certain powers, such as the ability to recommend how countries should respond. While it’s a legal lever the agency can use, it’s also a tool that can grab public attention and steer it to try to address burgeoning health threats. Such a declaration could further rally donors and member countries to increase funding.

The WHO can revisit its decision. In January 2020, for example, the WHO didn’t declare the emerging coronavirus crisis a PHEIC, only to do so a week later.

It's Time to Follow the Science. Join our Campaign!

America Is in the ‘Figure It out Yourself’ Era of the Pandemic

The Atlantic reported:

In 2018, while reporting on pandemic preparedness in the Democratic Republic of Congo, I heard many people joking about the fictional 15th article of the country’s constitution: Débrouillez-vous, or “Figure it out yourself.” It was a droll and weary acknowledgment that the government won’t save you, and you must make do with the resources you’ve got. The United States is now firmly in the débrouillez-vous era of the COVID-19 pandemic.

Across the country, almost all government efforts to curtail the coronavirus have evaporated. Mask mandates have been lifted on public transit. Conservative lawmakers have hamstrung what public-health departments can do in emergencies. COVID funding remains stalled in Congress, jeopardizing supplies of tests, treatments and vaccines.
Detection Dogs Sniff out Long COVID, Leading to Hopes for Better Therapy

Newsweek reported:

COVID-19 detection dogs can also detect long COVID-19 in people, according to new research by veterinarians in Germany.

Scientists at the University of Veterinary Medicine in Hannover found that canines specialized in sniffing out the SARS-CoV-2 virus were also able to determine samples of patients suffering from long COVID effects.

These symptoms can include headaches, breathlessness and a variety of cognitive dysfunction.

Previous scientific examination revealed that specialized dogs could identify samples of people suffering from acute COVID-19. Their abilities regarding long COVID had not been determined prior to the Hannover veterinarians’ pilot study.
Can Our Mitochondria Help to Beat Long COVID?

The Guardian reported:

At Cambridge University’s MRC Mitochondrial Biology Unit, Michal Minczuk is one of a growing number of scientists around the world aiming to find new ways of improving mitochondrial health. This line of research could help provide much-needed treatments for people with long COVID, as well as revolutionizing our understanding of everything from neurodegenerative illnesses such as Parkinson’s disease to the aging process.

Mitochondria, tiny tube-shaped structures that are found in their hundreds, sometimes thousands, in nearly all of our cells, are best known as the body’s power plants, continuously converting the food we eat into ATP, a complex chemical that acts as a form of energy currency for cells. Without ATP, every one of our cells, from the brain to the muscles, would lack the fuel they need to keep churning away, and our organs would swiftly grind to a halt.

While hacking the mitochondrial genome could change healthcare in years to come, finding more immediate ways of improving mitochondrial health could help the millions of people with long COVID and chronic fatigue syndrome, also known as ME/CFS.

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https://www.judicialwatch.org/

https://www.judicialwatch.org/jw-cel...m_term=members

Simply put, abortion ends a human life and is incompatible with a civil, moral society. The lives of unborn human beings must be protected in every state. States should immediately act to protect the lives of unborn human beings. And Congress should also move to protect unborn lives at the federal level. For example, Congress should move to stop, in the least, federal funding for the trafficking of fetal organs harvested from human beings killed by abortion.

https://trib247.com/articles/after-t...ign=Newsletter

After the jab: 'Nonstop excruciating pain,' deprived of her children, and facing homelessness

by: WorldTribune.com 06/27/2022 Source: WorldTribune.com

article and 3 embedded videos

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https://thewashingtonstandard.com/dr-carrie-madej-involved-in-plane-crash-in-surgery-pray/

Dr. Carrie Madej Involved In Plane Crash – Pray
Tim Brown / June 27, 2022

Dr. Carrie Madej was involved in a small plane crash alongside her boyfriend. Both are in the hospital with multiple fractures, and her boyfriend has a broken back and fractured skull.

Dr. Madej’s website is hosting a zoom prayer this evening at 6:30 PM EST. There are 100 spaces open to anyone who would like to pray. They are also streaming it on Instagram.

For more information, you can email them at info@carriemadej.com.

Dr. Madej had just texted me on Thursday to state that she would not be doing public speaking events for several months as the medical board is coming after her full force.

According to Alive 11:

WARM SPRINGS, Ga. — The Federal Aviation Administration is investigating a plane crash in Meriwether County on Sunday.

A pilot and passenger crashed at Roosevelt Memorial Airport in Warm Springs after reporting engine trouble. The two landed in the field north of the airport, according to the FAA.

It happened around 2:15 p.m. The FAA said they were flying a single-engine Piper PA-24.

According to Michael Watson, the chairman for the Meriwether County Airport Authority, the flight was on the way from St. Petersburg, Florida, near Tampa, to Newnan-Coweta County Airport when it experienced an engine issue as the plane started its descent. The flight was diverted south to Warm Springs, but crashed. Flight tracking website Flight Aware shows the path of the flight before the crash.

The FAA is working with the National Transportation Safety Board to determine a cause for the crash. Neither agency would provide specifics of the investigation.

There was no information about the condition of the two on board.

I have confirmed that Dr. Madej is in ICU and that she is expected to be released possibly on Tuesday.

Please keep her in your prayers.

This is a developing story.

Article posted with permission from Sons of Liberty Media

“How many lives could have been saved? Our government, the United States of America, forced people to get vaccines that had not been properly safety tested.

That’s the story. Is that the world you want to live in? That’s the result of what we’re doing.

We’ve studied this, we’ve scrutinized it, and now we know the U S government, by action of forcing people to get a vaccine in order to be employed, murdered people. That is the truth.

People have died because of blood clots and it was caused by the United States government, so the United States government has murdered its citizens.”

Del Bigtree

www.icandecide.org ( ICAN )

www.thehighwire.com

The End Justifies the Means

So much for science.

Pfizer and FDA and NIH policy. Lower standards to make the product get EUA by a certain date. Serious product inconsistency with the lipid nanoparticle from batch to batch. Iissue kept secret until late in the approval timeline and issue only "resolved" by lowering the standards and definitions to make it pass.

https://www.youtube.com/watch?v=i5TUTDABtgk

Leaked EMA Emails Reveal: Concern with Pfizer C-19 Vaccine Batch Integrity and the Race to Authorize

Jun 23, 2022
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Join The Conversation! | https://trialsitenews.com/
Trial Site News recently were able to review leaked internal emails from the European Medicines Agency (EMA) and meeting report between the agency and Pfizer. The EMA oversees the evaluation and supervision of medicinal products for the European Union. Like other regulatory health bodies, its main responsibility is to protect and promote public health. Snapshots of internal EMA email correspondence; a November 26, 2020, PowerPoint presentation from a pivotal meeting between Pfizer and the agency, as well as a confidential 43-page Pfizer report were provided by an anonymous source because of their trust in Trial Site’s commitment to transparency, accessibility, and accountability in furtherance of a highly ethical, quality-focused and public health-centric biomedical research industry.

Article Link | https://www.trialsitenews.com/a/what-...


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Former BlackRock Portfolio Manager Exposes Pfizer Fraud - Edward Dowd

First published at 14:23 UTC on June 29th, 2022.

INCREDIBLY GOOD interview with Edward Dowd!
“It’s a perfect cover for central banks to print money for an “emergency”….and also put into place medical tyranny systems as cover for the collapse of the financial system to prevent riots.”

“My overarching thesis is that this is cover, you see the global coordination all over the world and the medical systems that they’re putting in place to track, to limit travel, to prevent riots… it’s just a system of control because... I believe the social contract has been broken. People just don’t know that yet. All the pensions are broke, they’re just not going to be able to pay. They need to have a method of controlling the proletariat, so to speak.”

“I’m on record stating that, as the truth comes out, it will get worse, and they will triple-down. You’ve gotta think like a criminal. If you’re caught — and they’re getting caught — they’re not going to be able to hide the numbers of injuries and deaths, the mortuaries filling up, the insurance data — they’re caught! They know they’re caught. The general public doesn’t know they’re caught yet, but they’re caught. They have to triple-down and they have to go deeper into this, and it’s gonna get worse. It’s gonna get weird and ugly and messed up for the next several months. We will win — these criminals will be brought to justice, but I expect full-on chaos this year. It’s just the nature of how a criminal thinks.”

https://brandnewtube.com/watch/forme...VTdCHKOTq.html

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___________________

Here is the Twitter channel for Edward Dowd

https://twitter.com/DowdEdward/statu...60894900695040

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https://www.bitchute.com/video/9VpZOn0HK60s/

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Dr. David Martin Calls For Prosecutions: Fauci Knew Remdesivir Would Kill Thousands

First published at 14:23 UTC on June 29th, 2022.

Jim Fetzer

We FINALLY have the case that will see to Dr. Fauci getting locked up, once & for all! Dr. David Martin knows everything about the crimes that the FDA, CDC, & New World Order poster child, Tony Fauci have committed and is DETERMINED to lock each & every one of these reptilian Satanists up! His new breakthrough in accomplishing this, is to find patients who were vaccinated, hospitalized with Remdesivir, & resulting in their death!

https://rumble.com/v1a7gwj-dr.-david...d-kill-th.html

https://usawatchdog.com/up-to-700-mi...-david-martin/

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700 Million Worldwide Will Die from CV19 Vax by 2028 – Dr. David Martin


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700 Million Worldwide Will Die from CV19 Vax by 2028 – Dr. David Martin

By Greg Hunter On June 28, 2022 In Political Analysis 171 Comments

By Greg Hunter’s USAWatchdog.com

Dr. David Martin has a deep medical science and investment resume. Dr Martin also runs a company (M·CAM International) that finances cutting edge innovation worldwide. He is also one of the key people seeking justice in lawsuits suing medical companies and the federal government involved in delivering the so-called vaccines for CV19. In simple terms, according to Dr. Martin, the CV19 vaccines are “bioweapons.” Big Pharma and the government knew it and also knew it would cause massive deaths and permanent injuries. Dr. Martin says, “It’s going to get much worse. . . . It is not a Corona virus vaccine. It is a spike protein instruction to make the human body produce a toxin. . . . The fact of the matter is the injections are an act of bioweapons and bioterrorism. They are not a public health measure. The facts are very simple. This was premeditated. . . . This was a campaign of domestic terror to get the public to accept the universal vaccine platform using a known biological weapon. That is their own words and not my interpretation.”

How many will die from the CV19 bioweapons? Dr. Martin says, “By their own estimate, they are looking for 700 million people globally, and that would put the U.S. participation in that of the injected population as 75 million to 100 million people. . . . There are a lot of reasons why they hope it will be between now and 2028 because there is this tiny little glitch of the illiquidity of the Social Security, Medicare and Medicaid programs. So, the fewer recipients of Social Security, Medicare and Medicaid, the better. Not surprisingly, the recommendation was people over the age of 65 were the first ones to get injected.”

Dr. Martin thinks the catastrophic effects of the CV19 injections will hit the medical industry soon. Dr. Martin explains, “The dirty secret is . . . there are a lot of pilots having micro vascular and clotting problems, and that keeps them out of the cockpit, which is a good place to not have them if they are going to throw a clot for a stroke or a heart attack. The problem is we are going to see that exact same phenomenon in the healthcare industry and at a much larger scale. So, we now have, along with the actual problem . . . of people getting sick and people dying, we actually have that targeting the healthcare industry writ large. Which means we are going to have nurses and doctors who are going to be among the sick and dead. That also means the sick and the dying are also not going to get care.”

Dr. Martin and his group are suing everybody from President Biden along with the FDA, CDC, Pfizer, Moderna and many others over the deaths and injuries from the CV19 bioweapons fraudulently passed off as “vaccines.” The next big court case is July 6, 2022, in federal court in Utah. Dr. Martin contends “this is far worse” than the Nuremberg trials of Nazis after WWII and adds, “This is organized crime. . . . They have hidden behind the immunity shield that absolves them of product liability by naming the delivery of a bioweapon–a vaccination program. . . . This is actually a criminal act. This is an act of domestic terror, and it is an anti-trust violation. This is racketeering. This is old school racketeering, and it is no different than the mob in the 1920’s. This is old school racketeering for personal gain and profit at the expense of human lives. You need to call it what it is, and it’s organized crime. I would say the Nazis were better than the people who are doing this. . . . The real question is why did American citizens develop a weapon to kill Americans and get paid to do it? That is a morally outrageous question, and, unfortunately, almost no one is asking it.”

There is much more in the 1-hour and 3-minute interview.

Join Greg Hunter od USAWatchdog.com as he interviews Dr. David Martin, the top expert in the ongoing and unfolding CV19 vax genocide and litigation for 6.21.22.

https://www.youtube.com/watch?v=Sp8ciwi0CL8

https://www.youtube.com/watch?v=Sp8ciwi0CL8

Life Insurance CEO Reveals Deaths Are Up 40% Among Working People: "Just unheard of”

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Facts Matter with Roman Balmakov
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https://trib247.com/articles/the-new...ign=Newsletter

The new normal: Healthy young people dying 'suddenly'

by: WorldTribune.com 06/29/2022 Source: WorldTribune.com

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Nick Nemeroff
by WorldTribune Staff, June 29, 2022

Comedian Nick Nemeroff, 32.

Dani Hampson, 34, fiancée of UK X Factor star Tom Mann.

The 20-year-old nephew of actor Josh Gad.

All young. All healthy. All died "suddenly" and "unexpectedly" in the past few days.

"Fortunately for the vaccine makers, no health authority in the world is investigating these deaths because healthy young people dying in their sleep is the new normal," Steve Kirsch wrote in a June 21 analysis on substack.com.

"There is no question that young people are dying in their sleep at an extraordinary rate never seen before."

Nemeroff died on Monday, his family said in a statement mourning his “sudden passing.” The cause of his death was not released. He was in perfect health before passing.

Canada’s CBC News reported that his manager, Morgan Flood of Grand Wave Entertainment, said that Nemeroff “died in his sleep.”

After getting the vaccine in February of 2021, Nemeroff (some say jokingly) tweeted: "Ok so I got the vaccine and it did have a side effect...the area the needle went into (if I had to describe it I’d say like, on the top part of my upper arm. If that makes sense?) hurt a bit after. Seems ok now but honestly do NOT recommend getting it & wish I could take it back."

Hampson, who worked as a publicist, did not suffer from any known health problems and her cause of death is unknown. She died on the morning of what should have been her marriage to Mann, The Sun reported.

Mann posted on social media following Hampson's passing: “I can’t believe I am writing these words but my darling Dani - my best friend, my everything and more, the love of my life - passed away in the early hours of Saturday morning, 18th June. On what was supposed to be the happiest day of our lives ended in irreversible heartbreak."

Gad, the Frozen actor, announced Sunday that his 20-year-old nephew Marco died in his sleep.

IT Guy
@ITGuy1959
“The Frozen actor, 41, announced Sunday that his "brilliant, creative and loving" 20-year-old nephew Marco died in his sleep.”

Suddenlyitis tragically strikes again.

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"Healthy young kids rarely died in their sleep before the COVID vaccine rolled out," Kirsch noted in a previous substack post in which he noted the passing of the 17-year-old daughter of Illinois Democrat Rep. Sean Casten.

Gwen Casten was vaccinated and died in her sleep.

Kirsch noted: "Will Sean Casten use this as an opportunity to learn more about how dangerous the vaccines are? Unfortunately, that’s very unlikely to happen. I think he will convince himself that: his daughter’s death was “unexplained,” these unexplained deaths are ONLY happening to vaccinated kids is simply “bad luck” these deaths, which only started happening after the COVID vaccines rolled out, are “unexplained” and continue to be a cheerleader for the COVID vaccines. That’s the real tragedy here."

The following come straight from the vaccine adverse event reporting system VAERS:

• A healthy 7-year-old boy arrived at the hospital in a lethargic and listless state on Feb. 16, 2022, just 13 days after he received the Covid vaccine. The boy went into shock and had a cardiac arrest. The Emergency Department staff was unable to revive him, so pronounced him dead. (VAERS 2152560)

• A 7-year-old girl is found dead in her bed 11 days after vaccination. She developed a mild fever and a cough the day before her death. She tested negative for Covid, but positive for flu like several others in her family. She died on Dec. 10, 2021 (VAERS 1975356)

• An 8-year-old boy from Mississippi died 7 days after his second dose of Pfizer’s COVID vaccine after being found blue and lifeless at home. He was rushed to the hospital with a full code in process. A pulse was detected several times, but the boy ultimately died in the ICU. The medical report noted anaphylaxis, shock-associated circulatory or cardiac conditions and possible multisystem inflammatory syndrome. He did not have COVID but had been vomiting in the hours prior to his death on Feb 11, 2022. (VAERS 2109625)

• A healthy 13-year-old Michigan County boy died in his sleep three days after getting his second dose of a COVID-19 vaccine in mid-June. He had complained of fever and fatigue after the jab. (VAERS 1406840) The autopsy showed Jacob Clynick’s heart was enlarged and had fluid around it, but the subsequent report from the CDC and Michigan authorities denied finding any evidence that the vaccine caused the death of this previously healthy boy with no underlying medical conditions.

"Doctors will tell you: healthy kids do not die in their sleep unexpectedly for no reason," Kirsch wrote. "The COVID vaccine is the most likely cause, hands down, for any child who has been vaccinated with the COVID vaccine and later dies in their sleep."

Kirsch added: "Nobody in mainstream media thinks all of these deaths are a problem."

Here are some tragic reports which demonstrate the stunning new normal:

Tributes Pour Out For TikTok Star Cooper Noriega After Sudden Death

Bayside High student-athlete dies after collapsing during conditioning, Virginia Beach officials say

Visitation for Breathitt County football player announced

Obituary: Tyler Mescher, age 23 of Maria Stein, Ohio died unexpectedly

Port Jefferson High School alumnus, star athlete passes away at 19

Alabama men's basketball manager Charlie Wilson dies unexpectedly

Dayton Shares Statement on Death of Coach Anthony Grant’s Daughter

Baltimore City Public Schools student dies while on field trip in Cecil County

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"EU Renews Digital COVID Pass Despite 99% Negative Public Feedback"

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zerohedge.com

https://www.zerohedge.com/geopolitic...ublic-feedback

"Acting on a proposal of the European Commission, the European Parliament, as expected, voted yesterday to renew the EU Digital Covid Certificate for another year. The vote was 453 for, 119 against and 19 abstentions.

The certificate regulation had been scheduled to expire on June 30. Earlier this month, a delegation from the parliament had already reached a 'political agreement' with the Commission on renewing the certificate, thus making yesterday’s vote virtually a foregone conclusion.

The certificate regulation was originally adopted in June of last year, ostensibly to facilitate 'safe travel' between EU member states. But the EU digital certificate quickly evolved into the model and sometimes infrastructure for the domestic 'health' or Covid passes that would serve to restrict access to many other areas of social life over the following year.

The EU has opted to extend the covid certificate despite the overwhelmingly negative results of a public consultation on the subject that was launched by the European Commission under the heading of 'Have Your Say' and that was open to the public from February 3 to April 8. The consultation elicited over 385,000 responses – almost all of which appear to be opposed to renewal!

In a letter to the European Ombudsman that the French member of the parliament Virginie Joron posted on her Twitter feed, Joron writes:

I read hundreds of responses at random with my team. I did not find any in favor of extending the QR code [i.e. the digital certificate]. Based on this large survey, it seems obvious that virtually all the responses were negative...

The renewal of the Digital Covid Certificate does not mean that it will be immediately applied, but that the infrastructure will remain in place and that it can be applied if and when member states see fit to do so.

The current rules for holding a valid EU Digital Covid Certificate do not only, needless to say, discriminate against the unvaccinated, but also against natural immunity, which is treated as more ephemeral than vaccine-induced immunity.

Proof of completed primary vaccination makes a certificate valid for 270 days; proof of having received a booster dose confers unlimited validity for the moment. On the other hand, proof of 'recovery' – with a positive PCR test being the only accepted proof – only confers 180 days of validity."

zerohedge.comJune 28, 20220 Comments

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BREAKING: WE THE PATRIOTS USA JOINS AMERICA'S FRONTLINE DOCTORS IN MOURNING THE LOSS OF DR. VLADIMIR ZELENKO

We are deeply saddened to report that a hero has passed from our midst today. Dr. Vladimir "Zev" Zelenko has died at the age of 48 after a long battle with cancer. As an official partner of the organization he founded, America's Frontline Doctors (AFLDS), we join AFLDS in remembering this true Patriot and American hero. He not only touched lives, he saved them.


Read the full story and Dr. Zelenko's obiturary here.

Contributions in memoriam to Dr. Zelenko's Z-Freedom Foundation may be made in Zev's name by clicking the button below.[URL="https://www.zfreedomfoundation.com/"]
DONATE TO Z-FREEDOM FOUNDATION[/URL]

Jordan Schachtel @ dossier.substack.com
@JordanSchachtel
·
Jun 29, 2022
Just ran the numbers on Biden Admin's new vax deal w Pfizer.

The old deal gave Pfizer $19.50 a dose. They're now paying > $30. Pfizer raised price by over 50%.

The deal will bring Pfizer $9.5 billion. Their expected revenue is > $100B this year, shattering records.

Criminal.
Jordan Schachtel @ dossier.substack.com
@JordanSchachtel
·
Follow
None of the shots will be delivered under an FDA approved label.

And there is no real evidence the juice works for current strains

Additionally, there are already 100s of millions of unused doses sitting around, which makes this whole op resemble a sketchy laundering operation.
8:04 PM · Jun 29, 2022
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FDA Panel Advisor Admits Agency “LOST” Clinical Trial Data for Placebo Group Before Approving Experimental Vaccine for Babies and Toddlers (Video)

Earlier this month the Food and Drug Administration (FDA) authorized the mRNA vaccine for emergency use in young children, aged six months to five years old, after its advisory committee voted in favor of the experimental treatment, claiming that it has passed its clinical hurdles and is effective in preventing symptomatic infection without causing worrisome side effects.
However, in addition to ignoring the mountain of evidence showing the vaccines are regularly causing life-threatening injuries – especially in healthy children and young people, the FDA ‘experts’ have routinely skipped crucial steps in the testing process, allowing them to manipulate the data in order to suit their desired outcomes.

This inexcusable act of criminal malpractice was confirmed this month by the team leader of the FDA’s clinical review staff, Rachel Zhang, who explained during an advisory panel zoom call that the agency had lost the results from the placebo group during its clinical trials related to the decision to approve the experimental jab for America’s youngest children.

Without this data from the placebo group, the effectiveness of the vaccine cannot be measured against those who did not receive the treatment. Therefore, the clinical trial is meaningless. But the gaping hole in the results apparently doesn’t matter to the ‘experts’ at the FDA, who went ahead with the EUA approval anyway.“There is no efficacy data,” Zhang explained. “I guess it will have to come from real-world effectiveness,” she added glibly.

In other words, babies and toddlers are essentially vaccine guinea pigs that will provide the lost data. Remember, Zheng is the team leader of the FDA’s clinical review staff, which oversees the approval of new medical treatments.

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Moderna vaccine increases rate of myocarditis for young adults by 44 times — peer-reviewed study

by: WorldTribune.com 06/30/2022 Source: WorldTribune.com

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A peer reviewed study out of France has discovered mRNA Covid vaccines astronomically increase rates of potentially fatal myocarditis.

The study found the risk for the Moderna vaccine was the highest, increasing risk of myocarditis in young adults aged 18 to 24 by 44 times. For the Pfizer vaccine, the risk was found to increase by 13 times.

Incredibly, these numbers under-represent the total number of Covid-vaccine-related myocarditis cases.

The French study limited its sample groups to hospital discharge diagnoses. Therefore, it does not include cases who may have died before arriving at a hospital. It also does not include individuals whose symptoms were not severe enough to result in hospitalization, or those who have myocarditis but are not yet aware they do.

The study's design also did not include the effect of boosters, as they are not recommended for young adults in France. They are, however, mandated by colleges, universities, and many employers in the United States without regard to age or natural immunity.

Myocarditis is a potentially life threatening inflammation of the heart. It took the life of 16-year-old Ernest Ramirez, Jr. on a basketball court five days after he received the Pfizer vaccine. It has been associated with an unprecedented number of deaths among professional athletes in 2021 and 2022.

Related: Father of son killed by Covid vaccine reports enticement to fraud by FEMA, June 9, 2022
Related: Report has compiled 937 serious health issues, 620 deaths, for athletes after covid shots, April 21, 2022


By comparison, COVID-19 itself was found to increase risk of myocarditis by 9%. The result is, using this under-representative data set, that for young adults, the risk of suffering myocarditis is at least 8 and 30 times greater than the risk from infection itself, for the Pfizer and Moderna shots, respectively.

As Dr. Peter McCullough has pointed out, the relative risk from the vaccines is even higher, because a person might not contract Covid, thereby avoiding these risks altogether. Similarly, later variants of SARS-CoV-2 have been proving less harmful. By contrast, repeated vaccination through boosters may have a cumulative negative effect.

Related: Dr. McCullough: Risk of dying from the vaccine appears greater than of dying from Covid, November 2, 2021

Related: Dr. McCullough: Don't let your kids get the Covid vaccine, March 8, 2022

Dr. Sanjay Verma, MD, a cardiologist, believes that the CDC’s earlier findings suggesting the risk of myocarditis is greater from Covid infection than from mRNA vaccines were erroneously inflated by a factor of 4.5 times. The cause of this is that the CDC used officially confirmed PCR positive test numbers as the total number of infected. In reality, the data shows PCR testing recorded less than a quarter of all cases.

“Seroprevalence data as of Feb 21, 2022, reveals 75 percent (about 54 million) of all children have been infected compared to 12 million officially confirmed PCR+ ‘cases’,” Dr. Verma told the Epoch Times in an email.

“Thus far, CDC has not adjusted its COVID-19 morbidity and mortality data accordingly,” Dr. Verma added.

The French study examined 1,612 cases of myocarditis and 1,613 cases of pericarditis in France from May 12, 2021, to Oct. 31, 2021, from a population of 32 million people aged 12 to 50 years who received 46 million doses of mRNA vaccines.

Dachsie comment:

Be sure to seek the help of a doctor that you know won't automatically answer your question like "Doctor, do you think my having gotten the COVID vaccine could be causing my problems? by the doctor replying like "No, the vaccine has nothing to do with your symptoms."

There probably is a big difference in the quality of care you will see for your health problems from a doctor who responds in that way to such a question and a response that replies by telling you that 'yes, the vaccine appears to cause heart symptoms in some patients, so I will certainly take that information under consideration and make it a part of your record.'

_____________________

MYOCARDITIS

https://www.mayoclinic.org/diseases-conditions/myocarditis/symptoms-causes/syc-20352539

Overview

Myocarditis is inflammation of the heart muscle (myocardium). The inflammation can reduce the heart's ability to pump blood. Myocarditis can cause chest pain, shortness of breath, and rapid or irregular heart rhythms (arrhythmias).

Infection with a virus is one cause of myocarditis. Sometimes a drug reaction or general inflammatory condition causes myocarditis.

Severe myocarditis weakens the heart so that the rest of the body doesn't get enough blood. Clots can form in the heart, leading to a stroke or heart attack.

Treatment for myocarditis may include medications, procedures or surgeries.
Symptoms

Some people with early myocarditis don't have symptoms. Others have mild symptoms.

Common myocarditis symptoms include:

Chest pain
Fatigue
Swelling of the legs, ankles and feet
Rapid or irregular heartbeat (arrhythmias)
Shortness of breath, at rest or during activity
Light-headedness or feeling like you might faint
Flu-like symptoms such as headache, body aches, joint pain, fever or sore throat

Sometimes, myocarditis symptoms are like a heart attack. If you are having unexplained chest pain and shortness of breath, seek emergency medical help.
Myocarditis in children

When children develop myocarditis, symptoms may include:

Breathing difficulties
Chest pain
Fainting
Fever
Rapid breathing
Rapid or irregular heart rhythms (arrhythmias)

When to see a doctor

Contact your health care provider if you have symptoms of myocarditis. Symptoms of myocarditis can seem like a heart attack. Get emergency medical help if you have unexplained chest pain, rapid heartbeats or shortness of breath.

If you have severe symptoms, go to the emergency room or call for emergency medical help.

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Causes

Myocarditis may be caused by infections, some drugs and chemicals, or a condition that causes body-wide inflammation. Often, the cause of myocarditis isn't found.

Potential causes of myocarditis include:

Viruses. Many viruses have been linked to myocarditis, including those that cause the common cold (adenovirus); COVID-19; hepatitis B and C; parvovirus, which causes a mild rash, usually in children (fifth disease); and herpes simplex virus.

Gastrointestinal infections (echoviruses), mononucleosis (Epstein-Barr virus) and German measles (rubella) also can cause myocarditis. Myocarditis can also be caused by HIV, the virus that causes AIDS.
Bacteria. Bacteria that can cause myocarditis include staphylococcus, streptococcus, and bacteria that cause diphtheria and Lyme disease.
Parasites. Among these are Trypanosoma cruzi and toxoplasma. Some parasites are transmitted by insects and can cause a condition called Chagas disease. Chagas disease is much more common in Central and South America than in the United States.
Fungi. A fungal infection may cause myocarditis, particularly in people with weakened immune systems. Those linked to myocarditis include yeast infections, such as candida; molds, such as aspergillus; and histoplasma, often found in bird droppings.

Myocarditis may also be caused by:

Certain medications or illegal drugs (drug-induced myocarditis). These include drugs used to treat cancer; antibiotics, such as penicillin and sulfonamide drugs; some anti-seizure medications; and cocaine.
Chemicals or radiation. Exposure to carbon monoxide and radiation can sometimes cause heart muscle inflammation.
Other inflammatory diseases. Conditions that may cause myocarditis include lupus, Wegener's granulomatosis, giant cell arteritis and Takayasu's arteritis.

Complications

Usually, myocarditis goes away without permanent complications. However, severe myocarditis can permanently damage the heart muscle.

Potential complications of myocarditis may include:

Heart failure. Untreated, myocarditis can damage the heart muscle so that it can't pump blood well. In severe cases, myocarditis-related heart failure may require a ventricular assist device or a heart transplant.
Heart attack or stroke. If the heart muscle is injured and can't pump blood, the blood that collects in the heart can form clots. A heart attack can occur if a clot blocks one of the heart (coronary) arteries. A stroke can occur if a blood clot in the heart travels to an artery leading to the brain.
Rapid or irregular heart rhythms (arrhythmias). Damage to the heart muscle can change how the heart beats. Certain arrhythmias increase the risk of stroke.
Sudden cardiac death. Certain serious arrhythmias can cause the heart to stop beating (sudden cardiac arrest). It's deadly if not treated immediately (sudden cardiac death).

Prevention

There's no specific prevention for myocarditis. However, taking these steps to prevent infections might help:

Avoid close contact with people who are sick. Stay away from people with symptoms of the flu or other respiratory illness until they've recovered. If you're sick with symptoms of a viral infection, try to avoid exposing others.
Wash your hands regularly. Frequent hand-washing is one of the best ways to avoid getting sick and spreading illness.
Avoid risky behaviors. To reduce the chances of getting an HIV-related myocardial infection, practice safe sex and don't use illegal drugs.
Get recommended vaccines. Stay up to date on the recommended vaccines, including those that protect against COVID-19, influenza and rubella — diseases that can cause myocarditis. Rarely, the COVID-19 vaccine can cause inflammation of the heart muscle (myocarditis) and inflammation of the outer heart lining (pericarditis), particularly in males ages 12 to 29. Talk to your health care provider about the benefits and risks of vaccines.

By Mayo Clinic Staff

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Did US Biotechnology Help to Create COVID-19? | by Neil L. Harrison & Jeffrey D. Sachs - Project Syndicate
Neil L. Harrison & Jeffrey D. Sachs
11-13 minutes

While blaming China exclusively for COVID-19's apparent emergence in Wuhan, US authorities have suppressed inquiries into the role that US scientific research institutions may have played in creating the conditions for the pandemic. Yet if the coronavirus did indeed come from a lab, US culpability is almost certain.

NEW YORK – When US President Joe Biden asked the United States Intelligence Community to determine the origin of COVID-19, its conclusion was remarkably understated but nonetheless shocking. In a one-page summary, the IC made clear that it could not rule out the possibility that SARS-CoV-2 (the virus that causes COVID-19) emerged from a laboratory.

But even more shocking for Americans and the world is an additional point on which the IC remained mum: If the virus did indeed result from laboratory research and experimentation, it was almost certainly created with US biotechnology and know-how that had been made available to researchers in China.

To learn the complete truth about the origins of COVID-19, we need a full, independent investigation not only into the outbreak in Wuhan, China, but also into the relevant US scientific research, international outreach, and technology licensing in the lead-up to the pandemic.

We recently called for such an investigation in the Proceedings of the National Academy of Sciences. Some might dismiss our reasons for doing so as a “conspiracy theory.” But let us be crystal clear: If the virus did emerge from a laboratory, it almost surely did so accidentally in the normal course of research, possibly going undetected via asymptomatic infection.

It is of course also still possible that the virus had a natural origin. The bottom line is that nobody knows. That is why it is so important to investigate all the relevant information contained in databases available in the US.
Missed Opportunities

Since the start of the pandemic in early 2020, the US government has pointed an accusatory finger at China. But while it is true that the first observed COVID-19 cases were in Wuhan, the full story of the outbreak could involve America’s role in researching coronaviruses and in sharing its biotechnology with others around the world, including China.

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US scientists who work with SARS-like coronaviruses regularly create and test dangerous novel variants with the aim of developing drugs and vaccines against them. Such “gain-of-function” research has been conducted for decades, but it has always been controversial, owing to concerns that it could result in an accidental outbreak, or that the techniques and technologies for creating new viruses could end up in the wrong hands. It is reasonable to ask whether SARS-CoV-2 owes its remarkable infectivity to this broader research effort.

Unfortunately, US authorities have sought to suppress this very question. Early in the epidemic, a small group of virologists queried by the US National Institutes of Health told the NIH leadership that SARS-CoV-2 might have arisen from laboratory research, noting that the virus has unusual features that virologists in the US have been using in experiments for years – often with support from the NIH.

How do we know what NIH officials were told, and when? Because we now have publicly available information released by the NIH in response to a Freedom of Information Act (FOIA) request. We know that on February 1, 2020, the NIH held a conference call with a group of top virologists to discuss the possible origin of the virus. On that call, several of the researchers pointed out that laboratory manipulation of the virus was not only possible, but according to some, even likely. At that point, the NIH should have called for an urgent independent investigation. Instead, the NIH has sought to dismiss and discredit this line of inquiry.
Heads in the Sand

Within days of the February 1 call, a group of virologists, including some who were on it, prepared the first draft of a paper on the “Proximal Origin of SARS-CoV-2.” The final draft was published a month later, in March 2020. Despite the initial observations on February 1 that the virus showed signs of possible laboratory manipulation, the March paper concluded that there was overwhelming evidence that it had emerged from nature.

The authors claimed that the virus could not possibly have come from a laboratory because “the genetic data irrefutably show that SARS-CoV-2 is not derived from any previously used virus backbone.” Yet the single footnote (number 20) backing up that key claim refers to a paper from 2014, which means that the authors’ supposedly “irrefutable evidence” was at least five years out of date.

Owing to their refusal to support an independent investigation of the lab-leak hypothesis, the NIH and other US federal government agencies have been subjected to a wave of FOIA requests from a range of organizations, including US Right to Know and The Intercept. These FOIA disclosures, as well as internet searches and “whistleblower” leaks, have revealed some startling information.

Consider, for example, a March 2018 grant proposal submitted to the US Defense Advanced Research Projects Agency (DARPA) by EcoHealth Alliance (EHA) and researchers at the Wuhan Institute of Virology (WIV) and the University of North Carolina (UNC). On page 11, the applicants explain in detail how they intend to alter the genetic code of bat coronaviruses to insert precisely the feature that is the most unusual part of the SARS-CoV-2 virus.

Although DARPA did not approve this grant, the work may have proceeded anyway. We just don’t know. But, thanks to another FOIA request, we do know that this group carried out similar gain-of-function experiments on another coronavirus, the one that causes Middle East respiratory syndrome (MERS).

In yet other cases, FOIA disclosures have been heavily redacted, including a remarkable effort to obscure 290 pages of documents going back to February 2020, including the Strategic Plan for COVID-19 Research drafted that April by the US National Institute of Allergy and Infectious Diseases. Such extensive redactions deeply undermine public trust in science, and have only served to invite additional urgent questions from researchers and independent investigators.
The Facts of the Case

Here are ten things that we do know.

First, the SARS-CoV-2 genome is distinguished by a particular 12-nucleotide sequence (the genetic code) that serves to increase its infectivity. The specific amino acid sequence directed by this insertion has been much discussed and is known as a furin cleavage site (FCS).

Second, the FCS has been a target of cutting-edge research since 2006, following the original SARS outbreak of 2003-04. Scientists have long understood that the FCS holds the key to these viruses’ infectivity and pathophysiology.

Third, SARS-CoV-2 is the only virus in the family of SARS-like viruses (sarbecoviruses) known to have an FCS. Interestingly, the specific form of the FCS that is present in SARS-CoV-2 (eight amino acids encoded by 24 nucleotides) is shared with a human sodium channel that has been studied in US labs.

Fourth, the FCS was already so well known as a driver of transmissibility and virulence that a group of US scientists submitted a proposal to the US government in 2018 to study the effect of inserting an FCS into SARS-like viruses found in bats. Although the dangers of this kind of work have been highlighted for some time, these bat viruses were somehow considered to be in a lower-risk category. This exempted them from NIH gain-of-function guidelines, thereby enabling NIH-funded experiments to be carried out at the inadequate BSL-2 safety level.

Fifth, the NIH was a strong supporter of such gain-of-function research, much of which was performed using US-developed biotechnology and executed within an NIH-funded three-way partnership between the EHA, the WIV, and UNC.

Sixth, in 2018, a leading US scientist pursuing this research argued that laboratory manipulation was vital for drug and vaccine discovery, but that increased regulation could stymie progress. Many within the virology community continue to resist sensible calls for enhanced regulation of the most high-risk virus manipulation, including the establishment of a national regulatory body independent of the NIH.

Seventh, the virus was very likely circulating a lot earlier than the standard narrative that dates awareness of the outbreak to late December 2019. We still do not know when parts of the US government became aware of the outbreak, but some scientists were aware of the outbreak as of mid-December.

Eighth, the NIH knew as early as February 1, 2020, that the virus could have emerged as a consequence of NIH-funded laboratory research, but it did not disclose that fundamental fact to the public or to the US Congress.

Ninth, extensive sampling by Chinese authorities of animals in Wuhan wet markets and in the wild has found not a single wild animal harboring the SARS-CoV-2 virus. Despite this, there is no indication that the NIH has requested the laboratory records of US agencies, academic centers, and biotech companies involved in researching and manipulating SARS-like coronaviruses.

Tenth, the IC has not explained why at least some of the US intelligence agencies do in fact believe that a laboratory release was either the most likely or at least a possible origin of the virus.
Time for Transparency

Given the questions that remain unanswered, we are calling on the US government to conduct a bipartisan investigation. We may never understand the origin of SARS-CoV-2 without opening the books of the relevant federal agencies (including the NIH and the Department of Defense), the laboratories they support, academic institutions that store and archive viral sequence data, and biotechnology companies.

A key objective of the investigation would be to shed light on a basic question: Did US researchers undertake research or help their Chinese counterparts to undertake research to insert an FCS into a SARS-like virus, thereby playing a possible role in the creation of novel pathogens like the one that led to the current pandemic?

Investigations into COVID-19’s origins should no longer be secretive ventures led by the IC. The process must be transparent, with all relevant information being released publicly for use by independent scientific researchers. It seems clear to us that there has been a concerted effort to suppress information regarding the earliest events in the outbreak, and to hinder the search for additional evidence that is clearly available within the US. We suggest that a panel of independent researchers in relevant disciplines be created and granted access to all pertinent data in order to advise the US Congress and the public.

There is a good chance that we can learn more about the origins of this virus without waiting on China or any other country, simply by looking in the US. We believe such an inquiry is long overdue.