CORONA Main Coronavirus thread

marsh

On TB every waking moment
View: https://www.youtube.com/watch?v=YJZQmT5hJ8w
1:08 min

Understanding Vaccine Hesitancy

Jan 25, 2022


Johns Hopkins Bloomberg School of Public Health


There are many reasons why people may be hesitant or concerned about vaccines. This video provides a short overview of some of the key reasons that people may be vaccine hesitant. Learn more in our free online @Coursera course: https://www.coursera.org/learn/covid-...

^^^^^^
View: https://www.youtube.com/watch?v=tsA6m5HpHIs
1:28 min

How to Spot Vaccine Misinformation and Fake News

Jan 25, 2022


Johns Hopkins Bloomberg School of Public Health


With so much information out there it can be difficult to sift fact from fiction. This video walks you through a few key strategies that will help you identify vaccine misinformation. Learn more in our free online @Coursera course: https://www.coursera.org/learn/covid-...

*****
View: https://www.youtube.com/watch?v=9_QbT1BN0gE
1:39 min

The COVID-19 Vaccine Development and Approval Process in the U S

Jan 25, 2022


Johns Hopkins Bloomberg School of Public Health


This video provides a short explanation for the clinical trial and approval process for COVID-19 vaccines in the United States. Learn more in our free online @Coursera course: https://www.coursera.org/learn/covid-...
 

marsh

On TB every waking moment
View: https://www.youtube.com/watch?v=NZ4rZaMMN7I
10:52 min

Case Report About Vitamin D Deficiency in a Child and Long COVID with Virus Isolated in the GI Tract

Jan 25, 2022


MedCram - Medical Lectures Explained CLEARLY


Roger Seheult, MD of MedCram analyzes the case of an 11 year old female patient with long COVID, virus present in the GI tract, and evidence of vitamin D deficiency. (This video was recorded on January 25, 2022)

Roger Seheult, MD is the co-founder and lead professor at https://www.medcram.com He is Board Certified in Internal Medicine, Pulmonary Disease, Critical Care, and Sleep Medicine and an Associate Professor at the University of California, Riverside School of Medicine.

LINKS / REFERENCES: Persistent SARS-CoV-2 Nucleocapsid Protein Presence in the Intestinal Epithelium of a Pediatric Patient 3 Months After Acute Infection (JPGN) | https://journals.lww.com/jpgnr/Fullte... Vitamin D and COVID 19: The Evidence for Prevention and Treatment of Coronavirus (MedCram) | https://youtu.be/ha2mLz-Xdpg Sunlight: Optimize Health and Immunity (MedCram) | https://youtu.be/5YV_iKnzDRg
 

marsh

On TB every waking moment

FBI Searches Illinois 'Center For COVID Control' Headquarters Following Complaints: Officials

TUESDAY, JAN 25, 2022 - 06:35 PM
Authored by Jack Phillips via The Epoch Times (emphasis ours),

The FBI confirmed its agents searched the Illinois headquarters of the Center for COVID Control amid a federal investigation into the multimillion-dollar testing business.

“The FBI was conducting court-authorized law enforcement activity in Rolling Meadows [on Jan. 22],” FBI Chicago spokespeople told media in confirming the search of the business.


People stop outside a COVID-19 testing site in New York City on Jan. 10, 2022. (Scott Heins/Getty Images)

Yvonne Gamble, a spokesperson for the Health and Human Services (HHS) inspector general, said HHS agents and the FBI had searched the Rolling Meadows, Illinois, facility.

Annie Thompson, a spokesperson for the Illinois attorney general, told USA Today that the office is “working with the FBI and other law enforcement partners and will not comment on ongoing investigations as we work to hold accountable individuals who engage in unlawful conduct.”

The federal Centers for Medicare & Medicaid Services stated on Jan. 21 that it’s investigating “numerous complaints” associated with laboratories and testing sites run by the Center for COVID Control.

“We take seriously any allegations of fraud or misbehavior by COVID-19 testing sites. CMS’s Center for Clinical Standards and Quality investigates these kinds of complaints and is aware of several alleged instances of misconduct by this company’s labs,” Dr. Lee Fleisher, chief medical officer and director of the Center for Clinical Standards and Quality for CMS, told CNN in a statement.

The agency “identified non-compliance” on behalf of the Center for COVID Control “and is waiting on an allegation of compliance from the laboratory to address the deficiencies cited,” Fleisher said, without elaborating.

Earlier in January, the Center for COVID Control’s founder and CEO, Aleya Siyaj, announced that the company would suspend operations between Jan. 14 and Jan. 22 due to “unusually high patient demand” that has caused staffing shortfalls.

“Center for COVID Control is committed to serving our patients in the safest, most accurate and most compliant manner,” Siyaj said. “Regrettably, due to our rapid growth and the unprecedented recent demand for testing, we haven’t been able to meet all our commitments.”

Later, the company stated that “it is extending its pause on operations” and “remains committed to providing the highest level of customer service and diagnostic quality and will not resume collection of patient samples until staffing resources permit CCC to operate at full capacity.”

Minnesota Attorney General Keith Ellison also filed a lawsuit against the firm earlier in January, claiming it had failed to deliver COVID-19 test results, had delivered them in an untimely manner, or had provided falsified results.

People reported receiving COVID-19 results that were “riddled with inaccurate and false information including listing the wrong test type and false dates and times for when samples were collected from consumers,” his lawsuit read. Others got negative results when they hadn’t submitted samples to be tested, according to the suit.

Meanwhile, the Oregon Department of Justice told local media it would investigate the company for possible violations of state law.

The Center for COVID Control didn’t respond to a request from The Epoch Times for comment by press time.
 

marsh

On TB every waking moment
(Australia)


“I Have Had Every Symptom You Could Dream Of” – Bedridden Aussie Mayor Opens Up About Immune Reaction After Receiving COVID Vaccine

By Jim Hoft
Published January 25, 2022 at 7:35pm
AF02E6B0-76EB-4369-94FC-3161D1E3989F.jpeg


An Australian mayor is bedridden and has spent time in and out of the hospital after suffering a severe reaction to her second COVID vaccination, the West Australian reported.

Mayor Claire Boan of Port Adelaide Enfield opened up about her current condition and described “the new normal” in her life on her Facebook account last week.

According to the mayor, she’s been in bed for more than 35 days due to an immune reaction after receiving her second COVID shot.

“I have had every symptom you could dream of and my body continues to display new ones; it’s been exhausting for my body, traumatic for my family, and difficult for my mind,” the mayor said.

Here is her full statement:

This is my 35th day of receiving breakfast in bed. It’s usually a treat reserved for Mother’s Day or my birthday but for over a month, it has become the new normal in my life. Last night, I couldn’t put my kids to bed or check on them as they slept at night, and I haven’t done that for over a month, either.

I didn’t share any happy photos of Christmas or trips to the beach, no holidays in our camper, or smiles when we received our new baby guinea pigs.

Social media has been a place I’d share positive life experiences, celebrating achievements or funny anecdotes of our days. I usually keep the s#*t times pretty tight and share them with only my closest companions.

That is up until now…

I’ve been laid up in bed and in and out of the hospital with an immune reaction to my second vaccination. I have had every symptom you could dream of and my body continues to display new ones; it’s been exhausting for my body, traumatic for my family, and difficult for my mind.

For 2 years now, I’ve been speaking against the constant voices of fear being broadcast from all directions; and, in more recent times, the division rising across our country and community. So, as I lay in bed feeling next to useless, I’m continuing to find ways to share a voice of kindness and hope. True leaders are encouraging, empathetic, honest, demonstrate true courage, and admit faults or wrongdoings. I’ve been learning a whole new level of vulnerability throughout this time; something I’ve spoken about many times over but am now understanding a whole new level of what this means. Good leaders know how to share about vulnerable times, too.

So, as one day rolls into the next, with no understanding of when I’ll be able to play with my kids, run on the beach, cook a family dinner or spend time in my garden (and of course then return fully to the most wonderful job I have the privilege of having), I want to leave a reminder with you all. Please…Be kind. Show empathy. Demonstrate an open heart. Be the best you.



When are the Aussies going to wake up and realize that the vaccines are not safe and effective?
 

marsh

On TB every waking moment

Top American Medical Journal Study Confirms the Risk of Myocarditis and Pericarditis After Receiving COVID-19 Vaccines – Risks is Highest After Second Vaccine in Adolescent Males and Young Men

By Jim Hoft
Published January 25, 2022 at 9:00pm

A new study released on Tuesday by the Journal of the American Medical Association (JAMA) revealed the development of myocarditis and pericarditis after mRNA-based COVID-19 vaccination which is highest in adolescent males and young men.

The study was based on the data from VAERS on reported cases of myocarditis that occurred after receiving the Pfizer and Moderna vaccine between December 2020 and August 2021 in 192, 405 ,448 individuals older than 12 years of age in the US. These data were processed by VAERS as of September 30, 2021.

The primary outcome after the vaccination was the occurrence of myocarditis and the secondary outcome was pericarditis.

According to the study, VAERS received 1,991 reports of myocarditis (391 of which also included pericarditis) after receipt of at least 1 dose of mRNA-based COVID-19 vaccine and 684 reports of pericarditis without the presence of myocarditis.

Of the 1991 reports of myocarditis, 1,626 met the CDC’s case definition for probable or confirmed myocarditis. (See table below)

Screen-Shot-2022-01-25-at-7.52.16-PM.jpg


From Journal of the American Medical Association:

Findings In this descriptive study of 1,626 cases of myocarditis in a national passive reporting system, the crude reporting rates within 7 days after vaccination exceeded the expected rates across multiple age and sex strata.

Screen-Shot-2022-01-25-at-8.25.44-PM.jpg


The rates of myocarditis cases were highest after the second vaccination dose in adolescent males aged 12 to 15 years (70.7 per million doses of the BNT162b2 vaccine), in adolescent males aged 16 to 17 years (105.9 per million doses of the BNT162b2 vaccine), and in young men aged 18 to 24 years (52.4 and 56.3 per million doses of the BNT162b2 vaccine and the mRNA-1273 vaccine, respectively).

Meaning Based on passive surveillance reporting in the US, the risk of myocarditis after receiving mRNA-based COVID-19 vaccines was increased across multiple age and sex strata and was highest after the second vaccination dose in adolescent males and young men.

Main Outcomes and Measures Reports of myocarditis to VAERS were adjudicated and summarized for all age groups. Crude reporting rates were calculated across age and sex strata. Expected rates of myocarditis by age and sex were calculated using 2017-2019 claims data. For persons younger than 30 years of age, medical record reviews and clinician interviews were conducted to describe the clinical presentation, diagnostic test results, treatment, and early outcomes.

Results Among 192, 405,448 persons receiving a total of 354,100,845 mRNA-based COVID-19 vaccines during the study period, there were 1,991 reports of myocarditis to VAERS, and 1,626 of these reports met the case definition of myocarditis. Of those with myocarditis, the median age was 21 years (IQR, 16-31 years) and the median time to symptom onset was 2 days (IQR, 1-3 days).

Males comprised 82% of the myocarditis cases for whom sex was reported. The crude reporting rates for cases of myocarditis within 7 days after COVID-19 vaccination exceeded the expected rates of myocarditis across multiple age and sex strata. (See graph below)

The rates of myocarditis were highest after the second vaccination dose in adolescent males aged 12 to 15 years (70.7 per million doses of the BNT162b2 vaccine), in adolescent males aged 16 to 17 years (105.9 per million doses of the BNT162b2 vaccine), and in young men aged 18 to 24 years (52.4 and 56.3 per million doses of the BNT162b2 vaccine and the mRNA-1273 vaccine,
respectively). There were 826 cases of myocarditis among those younger than 30 years of age who had detailed clinical information available; of these cases, 792 of 809 (98%) had elevated troponin levels, 569 of 794 (72%) had abnormal electrocardiogram results, and 223 of 312 (72%) had abnormal cardiac magnetic resonance imaging results. Approximately 96% of persons (784/813) were hospitalized and 87% (577/661) of these had resolution of presenting symptoms by hospital discharge. The most common treatment was nonsteroidal anti-inflammatory drugs (589/676; 87%).

Screen-Shot-2022-01-25-at-8.26.16-PM.jpg


Conclusions and Relevance Based on passive surveillance reporting in the US, the risk of myocarditis after receiving mRNA-based COVID-19 vaccines was increased across multiple age and sex strata and was highest after the second vaccination dose in adolescent males and young men. This risk should be considered in the context of the benefits of COVID-19 vaccination.

Read the full study here:

Myocarditis Cases Reported After mRNA-Based COVID-19 Vaccination in the US From December 2020 to August 202… by Jim Hoft on Scribd (Scribd doc on website)

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Download this PDF
 

marsh

On TB every waking moment

Yep, They're Still Riding The "Omicron" Wave...

TUESDAY, JAN 25, 2022 - 05:55 PM
Authored by Michael Tracey via Substack,

I’m still constantly receiving these little reports from across the US (and Canada!) detailing the petty indignities and absurdities to which people are subjected in the name of this-or-that overheated COVID concern.

Does every last report amount to full-blown authoritarian tyranny? Not really — most probably wouldn’t even register as particularly attention-getting on their own. But the thing I keep coming back to is the cumulative pettiness — how corrosive the sheer quantity of snippets like ones I’ll list in this post, taken in aggregate, must be to the social order.



Which makes the “Omicron” subject, however tiresome, impossible to avoid — much as one might wish to focus on other things, and even as media outlets have begun to acknowledge that the “wave” has “crested.” Because the thing about waves is that they recede, and then they come back, and then the process repeats for eternity. Hence why the eternal-seeming quality of these measures is of particular note. I know this is a wearying and increasingly boring topic; yet there really is a de facto “gag order” in place at so many institutions still laboring under ridiculous protocols, even approaching the two year mark of this whole ordeal, and even with the most frantic segment of COVID-fixators increasingly confined to a somewhat marginal fringe.

For instance, a journalist recently contacted me about COVID-related policy excesses taking place in a particular jurisdiction. The journalist was frustrated that these excesses were not being given sufficient attention. And he/she was right — although I’m purposely not naming the jurisdiction here for maximum discretion, because the journalist was simultaneously adamant that his/her name not be mentioned in any forthcoming report I may do on the matter.
“Some people I work with and many in the media tend to lean heavy on being pro-COVID restrictions,” the journalist told me, “and I’d like to not be associated with the controversy… Perhaps call it cowardice and self-censorship, but I just got this job and don’t want to jeopardize sources/contacts.”
So: even if you personally feel no inhibition about criticizing ridiculous COVID protocols, even if you’re openly scornful of “Omicron” somehow necessitating the re-imposition of various kinds of hygiene theater, and even if you inhabit a social/professional milieu where there is no taboo against maligning “public health” apparatchiks — please just realize there are millions of people who find themselves in a radically different position. Yes, even now, regardless of “Omicron” supposedly ebbing, and despite much of the country having long ago ceased to treat anything COVID-related as important to their lives.

Still, there are a multitude of contexts in which publicly objecting to various aspects Omicron-mania, no matter how narrowly-tailored those objections may be, could automatically place you under a cloud of suspicion — whereby you’re tarnished as “anti-vax” (regardless of whether you are personally vaccinated.) And of course, being “anti-vax” is widely viewed as interchangeable with being dangerously right-wing, which would also make you presumably sympathetic to “insurrectionists” — or perhaps even an “insurrectionist” yourself. Should we get the FBI on the phone, sir? The “MAGA” connotation here is especially odd, given that Donald Trump could not be more resolute in staking out an unwaveringly pro-vaccine stance, but the logical progression doesn’t have to make sense. This is more or less the school of thought that still, yes, today, dictates the social expectations at a wide variety of institutions, leading to absurdities of the kind that I’m about to list here. Someone’s gotta collect these, I guess, for posterity. Notwithstanding how very tedious it is. So, that’s what I’m doing.

Here’s a wild one I was told about recently: Oberlin College. Are you familiar with it? Depending on your level of familiarity, it may or may not surprise you that the dramatic “return to campus” earlier this month was accompanied by a host of hyper-scrupulous measures to ensure maximum Safety for the Community™. Professors — yes, fully accredited professors — were enlisted as emergency food delivery attendants for students consigned to “isolation.” This process entailed intensive “training” sessions, including instruction on the “Knock, Drop, Depart” rule, as well as how to accommodate students’ special dietary needs. (By the way, Oberlin recently laid off a huge percentage of its actual food service staff.)



Did you think “travel bans” were a thing of the past? Not at Princeton University, where students have been prohibited from traveling outside of Mercer County, NJ. (Mercifully, they’re also allowed to go to Plainsboro Township, in adjoining Middlesex County.) Anyone brazen enough to seek an exemption must undergo an unspecified “vetting process,” according to Dean Jill Dolan, who I hope it’s not rude to note is a Theater professor moonlighting as the university’s chief epidemiologist and emergency behavioral scientist. She previously ran the Gender and Sexuality Studies program. Here’s an excerpt from a recent town hall-style session in which Dean Dolan addresses carefully-moderated student queries:



And here is the highly scientific, evidence based, scrupulously empirical justification set forward by Dean Dolan for the travel ban:



Repeat after me: Keep our community safe. Keep our campus safe. We will be safe if you all behave safely. Safety is our first priority. If you’re not with us, you’re with the virus. Still today, at places like Princeton, grievances can often only be aired in private about the constant dreary pronouncements from official authorities purporting to be so very concerned for your health and safety, yadda yadda yadda.

Moving away from the always-fertile ground of college-based inanity for a moment, how about this: a few weeks ago, a guy showed up to accompany his pregnant wife for an ultrasound appointment in Washington State… only to be greeted by the familiar sight of an ALL CAPS notice posted sternly to the door, informing him that he was unable to attend the appointment on “safety” grounds. He was therefore deemed an ineligible “guest,” despite being one of two people directly involved in the impregnation process. Inquiries with the individual working at the front desk did not yield much in the way of fruitful clarifying information, as one might expect.



Unvaccinated middle schoolers were barred from taking part in extracurricular activities in San Jose, CA, where — by the way — a first-of-its-kind “booster” requirement was also recently enacted.

That is to say, in order to attend a San Jose Sharks hockey game or any other “large” event taking place at a city-owned facility, one must now provide proof not just of vaccinated status, but “boosted” status. In other words, you’re no longer “fully vaccinated” unless you’re thrice-vaccinated for the purposes of attending an NHL game. Enjoy.



And here’s a friendly “Double Masking Requirement” that was decreed at the University of Pennsylvania:



Trust me when I say I could go on and on with this. And the above items are all from just the past month. Question: regardless of whether you’re personally in a position to ignore such decrees, for which you should be thankful, do you have confidence that the “wave” is ever going to be declared officially “receded” at places like these? Or is it only a matter of time before they bureaucratize another “tsunami” into existence?
 

marsh

On TB every waking moment

Pfizer Begins Human Trials For New Omicron Vaccine As US Cases Tumble

TUESDAY, JAN 25, 2022 - 05:35 PM
Pfizer and its partner BioNTech just launched the first human trials of their revised COVID vaccine which has been adapted to try and provide better protection against the omicron variant. Shortly after the emergence of omicron in late November, Pfizer and its rivals all promised to produce another generation of vaccines, claiming they could have them ready within three months.

So far at least, that timeline appears mostly on track. However, an even more important question for Pfizer might be this: who will even need these jabs when they're ready, since it looks like the omicron wave numbers will have finally tapered off by the time the trials are completed.


At any rate, the two firms said Tuesday they had begun enrolling adults ages 18 to 55 for trials taking place in the US and South Africa. The trials will seek to examine the safety, tolerability and, most importantly, the immune response generated by the new vaccines, per WSJ. The big question will be whether they do what their makers have created them to do, or not.

At least one human subject has already received a shot of the new vaccine, Pfizer said Tuesday. Initial trial results are expected some time during the "first half of the year". But Pfizer CEO Albert Bourla has said that the company could receive approval for the jab from federal regulators as early as March.

Dr. Fauci still believes it's "entirely conceivable" that a fourth booster will be needed, as we reported the other day. And speaking on MSNBC earlier, the good doctor warned that it would be "prudent" to prepare for the likelihood that omicron will persist at pandemic levels for some time. He even stressed that an omicron-focused vaccine would help humanity prepare for the eventuality that the omicron-driven wave persists.

Video 4:26 min


However, case numbers have fallen substantially in South Africa, while also appearing to have turned the corner in the US, UK and elsewhere across Europe, globally, the number of newly confirmed cases of the virus has continued to rise.



Despite Bourla's cheery rhetoric about the possibility of only requiring one COVID booster per year, US regulators are already questioning whether more jabs are even necessary it seems. US health authorities have said that boosters targeting omicron might not be needed, since it's unclear whether future dominant variants will be descents of omicron, or other strains.

Research shows that certain mutations in the omicron variant allow it to more effectively bypass what little protections vaccines from Pfizer and Moderna actually offer.

As for the new trials, the two firms said they would test how the vaccine performs in three groups of volunteers, with some of the subjects coming from the study that led to the current vaccine’s clearance in 2020. Researchers plan to enroll up to 615 people who received the two-dose primary series of the current vaccine 3-6 months prior to their enrollment.

Once enrolled, they will receive either one dose of the omicron-focused vaccine, two doses four weeks apart from each other, or a third dose. Additionally, researchers will also recruit up to 600 people who received three doses of the current vaccine 3-6 months ago. These subjects will receive either one dose of the omicron jab, or a fourth dose of the current shot.
 

marsh

On TB every waking moment

Judge Saves New York's Mask Mandate After Last-Minute Appeal From Democrats

TUESDAY, JAN 25, 2022 - 05:19 PM
Update (1710ET): It looks like the New York Democrats led by Gov. Kathy Hochul have succeeded in protecting their precious mask mandates - for now, at least.

NY AG Letitia James announced Tuesday afternoon shortly after the end of the market day that a judge had granted the government's request for a stay while they look to appeal the ruling from the State Supreme Court.

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Not that NYC had planned to obey the justice's decision anyway. During a radio appearance on Tuesday morning, NYC Mayor Eric Adams said that he would order the mask mandate must continue to be observed in the city's schools for the public's safety - or so he said. He also labeled the court's ruling "unfortunate". The so-called "Hochul rule" required that masks be worn in public schools.
"I believe it’s unfortunate that it was struck down, and I believe those jurisdictions that are using it as an opportunity to remove mandates are making a big mistake. We need to follow the science, not the fears that is actually coming with this virus," he said on 1010 WINS.
It's just one more reason for anybody fed up with the Empire State's strict COVID restrictions to seriously consider seeking greener pastures, perhaps in a state with a much lower (or even non-existent) income tax.

* * *
In a decision that will likely be welcomed by many New York parents and schoolchildren, along with the countless workers, consumers and tourists in the Empire State, the Supreme Court of New York struck down Gov. Kathy Hochul's statewide mask mandate. In its ruling, the court declared the mask mandate "unconstitutional" and "null, void and unenforceable".

New York State Supreme Court Justice Thomas Rademaker of Nassau County wrote in his opinion explaining the decision that the governor doesn't have the authority to impose the mandate since the "emergency powers" once wielded by her predecessor, Gov. Andrew Cuomo, are no longer in place.

Without the assent of the legislature, the Court determined that the governor doesn't have the ability to order masks mandates, although the circumstances would be different if emergency powers granted by lawmakers were still in effect.


Gov. Hochul

The ruling goes: "While the intentions of Commissioner Bassett and Governor Hochul appear to be well-aimed squarely at doing what they believe is right to protect the citizens of New York State, they must take their case to the State Legislature."

Gov. Hochul ordered the mandate last month amid a flurry of new restrictions ordered by various states. President Biden has seen SCOTUS and another federal judge overrule his vaccination mandates.

In response to the ruling, Gov. Hochul said the following: "My responsibility as Governor is to protect New Yorkers throughout this public health crisis, and these measures help prevent the spread of COVID-19 and save lives. We strongly disagree with this ruling, and we are pursuing every option to reverse this immediately."

Put another way, Gov. Hochul says she doesn't care about the legal precedent, and will do everything in her power to continue enforcing the mandate.
We wonder how the Empire State's business community feels about the governor's pledge to find a way around the ruling?
 

marsh

On TB every waking moment

Psaki Suggests Monoclonal Antibodies 'Don't Work' Against Covid In Bumbling Defense Of FDA Decision

TUESDAY, JAN 25, 2022 - 11:10 AM
Update (1527ET): Jen Psaki's real-time propaganda is truly something to behold.


When asked on Tuesday about the FDA's decision to yank the Emergency Use Authorization for monoclonal antibodies, the White House press secretary spat out a word-salad of disinformation.

"Let's just take a step back here just to realize how crazy this is," Psaki began, reading her answer. "We've approached Covid treatments like filling a medicine cabinet. We're not relying on one type, one brand, or treatment. We invested in, and continue to buy a variety across [sic] monoclonal antibodies, pre-exposure prevention therapies, and oral antivirals.

"What the FDA is making clear is that these treatments, the one that they are fighting over - that the governor is fighting over - do not work against Omicron, and they have side effects. That is what the scientists are saying.

Psaki then put monoclonals on par with 'advocating for things that don't work, even though we know things do work; injecting disinfectant, promoting other pseudo-science, sowing doubt on the effectiveness of vaccines and boosters, and now promoting treatments that don't work."

Watch:

View: https://twitter.com/i/status/1486056528356515847
1:49 min
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In a January preprint, researchers at UC Berkeley and other institutions found that "some monoclonal antibodies will not be useful in treating Omicron-infected patients," but that "Casirivimab was able to neutralize OmC3 but not OmC1 and Imdevimab was able to neutralize OmC1 but not OmC3."

So clearly a reduced efficacy - much like the vaccines - against Omicron, but it's patently false to say they're a treatment that 'doesn't work.'

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* * *
Governor Ron DeSantis is demanding the Biden Administration reverse its sudden decision to revoke emergency use authorization (EUA) for monoclonal antibody treatments.



In a statement from the Florida Governor's office, he rages that this abrupt and unilateral action by the Biden Administration will prevent access to lifesaving treatments for Floridians and Americans.

“Without a shred of clinical data to support this action, Biden has forced trained medical professionals to choose between treating their patients or breaking the law,” said Governor Ron DeSantis.
“This indefensible edict takes treatment out of the hands of medical professionals and will cost some Americans their lives. There are real-world implications to Biden’s medical authoritarianism – Americans’ access to treatments is now subject to the whims of a failing president.”
“Rather than giving Americans the option for various COVID treatments, the FDA and the Biden Administration issued their royal decree, taking away the very thing that is proven to reduce hospitalizations and save lives,” said Lieutenant Governor Jeanette Nuñez.
“Monoclonal antibody treatments like Regeneron have had a positive impact for thousands of Floridians. For the CDC and FDA, which have been consistently inconsistent throughout the entire pandemic, to restrict treatment does nothing but put individuals at risk.”
“In our field of medicine, when someone comes to you seeking a treatment that could save their life, it is essential to have treatment options to ensure health care providers can make the best decisions for their patients,” said Surgeon General Dr. Joseph Ladapo.
“The Federal Government has failed to adequately provide the United States with adequate outpatient treatment options for COVID-19. Now, they are scrambling to cover up a failure to deliver on a promise to ‘shut down the virus.’”
As a result of this abrupt and clinically unsupported action, the appointments for more than 2,000 Floridians to receive this treatment were canceled on January 25, 2022, alone. This decision was made solely by Biden’s Food and Drug Administration (FDA) without advance warning to states or health providers and without clinical data to support the decision. The deliberate decision by the Biden Administration to make this announcement effective immediately, through a press release, actively prevents states and health care providers from making real-time operational decisions that save lives.

Over the course of the past two years, scientists and researchers across the nation have worked hard to bring us treatments that are both safe and effective. One of these treatments has been monoclonal antibodies. This treatment has saved thousands of lives in Florida and across our nation.

* * *
Benny Johnson had an alternate take on the FDA's strange decision:
Biden canceling proven life-saving treatment for the sick and elderly so Fauci-Pfizer can get a few extra points in the stock market is literally demonic
A theme of regulator-capture that was echoed almost uniformly yesterday.

* * *
As Mimi Nguyen Ly detailed earlier at The Epoch Times, The U.S. Food and Drug Administration (FDA) announced Jan. 24 it is restricting the use of two monoclonal antibody treatments for COVID-19, saying data show such treatments are “highly unlikely” to be active against the Omicron variant, currently the dominant strain in the country.



Monoclonal antibodies are laboratory-created proteins that mimic natural antibodies the body produces to fight off harmful pathogens, such as the CCP (Chinese Communist Party) virus, also known as the novel coronavirus.

The agency revised its emergency authorization for the two COVID-19 treatments that come from Regeneron and Eli Lilly. Their use is now limited to when the COVID-19 patient is “likely to have been infected with or exposed to a variant that is susceptible to these treatments.”
Because data show these treatments are highly unlikely to be active against the omicron variant, which is circulating at a very high frequency throughout the United States, these treatments are not authorized for use in any U.S. states, territories, and jurisdictions at this time,” the FDA stated.

“In the future, if patients in certain geographic regions are likely to be infected or exposed to a variant that is susceptible to these treatments, then use of these treatments may be authorized in these regions.”
The Omicron variant, which started spreading in the United States in late November 2021, is estimated to account for more than 99 percent of cases in the country as of Jan. 15, according to data from the Centers for Disease Control and Prevention (CDC).

Rationale
The move to revise the emergency authorization “avoids exposing patients to side effects, such as injection site reactions or allergic reactions, which can be potentially serious, from specific treatment agents that are not expected to provide benefit to patients who have been infected with or exposed to the omicron variant,” the FDA stated.

The move was recently recommended by the COVID-19 Treatment Guidelines Panel, part of the National Institutes of Health (NIH) on Dec. 23, 2021. At the time, the panel said the Omicron variant “is predicted to have markedly reduced susceptibility” to several COVID-19 monoclonal antibodies, “especially bamlanivimab plus etesevimab and casirivimab plus imdevimab.” Eli Lilly’s monoclonal antibody treatments offers bamlanivimab and etesevimab, and Regeneron offers casirivimab and imdevimab.


The drug Bamlanivimab. (Courtesy of Eli Lilly via AP)

The panel added that GlakoSmithKline’s (GSK’s) and Vir Biotech’s antibody treatment, sotrovimab, “appears to retain activity against the Omicron variant.”

The U.S. Department of Health and Human Services (HHS) on Dec. 23, 2021, temporarily halted distribution of Regeneron’s and Eli Lilly’s antibody therapies, leaving sotrovimab as the only available treatment at the time.

Distribution was resumed after after complaints from governors, including Florida Gov. Ron DeSantis, who asserted the two monoclonal antibody treatments continued to help some COVID-19 patients. At the time, Omicron was circulating but the Delta variant was still the dominant variant in the United States.

The federal government has, since early January, shipped enough doses of the two monoclonal antibody treatments to treat more than 300,000 patients.

A Regeneron spokesperson had said the regulator would provide any potential communication on the topic. Lilly had no immediate comment but pointed to its statement from December 2021 saying its newer antibody candidate, bebtelovimab, maintains neutralization activity against all known variants of concern, including Omicron. The company said earlier this month it is “urgently working with the FDA to make bebtelovimab available under an emergency use authorization,” with a decision expected before April.


Patients wait for their treatment inside the Regeneron Clinic at a monoclonal antibody treatment site in Pembroke Pines, Florida, on August 19, 2021. (Chandan Khanna/AFP via Getty Images)

Both companies previously announced they were developing new antibodies that target the Omicron variant. Regeneron stated in December 2021, “While Regeneron’s currently authorized REGEN-COV antibodies have diminished potency against Omicron, they are active against Delta, which currently is the most prevalent variant in the U.S.”

Other Treatments
The revision in emergency authorization comes days after the FDA on Jan. 21 expanded approval of the antiviral drug remdesivir to treat more COVID-19 patients. Remdesivir was the first government-approved drug for COVID-19 and was previously limited to treat hospitalized patients. It is now authorized for use in adults and children aged 12 and above early in a COVID-19 infection if the patient faces a high risk of ending up in hospital.

The agency said its move was supported by a study run by the drug’s developer, Gilead Sciences, results of which showed that the drug reduced the risk of hospitalization by 87 percent among COVID-19-positive people. The FDA didn’t cite any independent studies.

The FDA in its statement on Jan. 24 pointed to several other therapies that “are expected to work against the Omicron variant,” intended for patients with mild-to-moderate COVID-19 to prevent progression to severe disease. They include sotrovimab, remdesivir, as well as two new antiviral pills from Pfizer and Merck, Paxlovid and molnupiravir, both of which are in short supply.
GSK and Vir Biotech are boosting production of their sotrovimab to help meet demand in the United States.

Remdesivir has been linked to kidney disease, gastrointestinal symptoms, and other severe side effects, according to some researchers. According to the FDA, some adverse events associated with remdesivir include allergic reaction, generalized seizure, rash. The WHO in late 2020 recommended against the use of remdesivir for COVID-19.

Pfizer’s Paxlovid is not recommended in those with severe kidney disease, according to the FDA. The agency also warns that “caution should be exercised” in giving Paxlovid to people with pre-existing liver diseases.

Meanwhile, some experts have expressed concerns about how Merck’s molnupiravir attacks the CCP virus, saying the pill has the potential to contribute to the development of cancer or cause birth defects in an unborn baby.

According to the FDA, sotrovimab may trigger a range of allergic reactions following infusion. The agency also noted, “It is possible that sotrovimab could interfere with your body’s own ability to fight off a future infection of SARS-CoV-2.

“Similarly, sotrovimab may reduce your body’s immune response to a vaccine for SARSCoV-2. Specific studies have not been conducted to address these possible risks. Talk to your healthcare provider if you have any questions.”
 

marsh

On TB every waking moment

WHO Chief Says Europe Moving Towards Pandemic "Endgame"

TUESDAY, JAN 25, 2022 - 03:30 AM
Authored by Paul Joseph Watson via Summit News,

Hans Kluge, the World Health Organization’s Europe director, says the continent is moving towards an “endgame” scenario, in another sign that Omicron heralds the beginning of the end of the pandemic.


Despite record cases being recorded in multiple different countries, Kluge told AFP that the milder nature of Omicron means COVID-19 could finally be on the path towards becoming endemic.
“It’s plausible that the region is moving towards a kind of pandemic endgame,” said Kluge.

“There will be for quite some weeks and months a global immunity, either thanks to the vaccine or because people have immunity due to the infection, and also lowering seasonality,” he added.
The health official predicted that there will now be a sustained period of declining case numbers, or “quiet” as he called it, before, “Covid-19 may come back towards the end of the year, but not necessarily the pandemic coming back.”

Kluge noted that hospitals will now be able to focus on people who have missed urgent health screenings due to lockdown measures.
“Stabilizing means that the health system is no longer overwhelmed due to Covid-19 and can continue with the essential health services, which have unfortunately been really disrupted for cancer, cardiovascular disease, and routine immunization,” he said.
Despite the pandemic being on its way out, technocrats are still attempting to entrench the ‘new normal’ that arrived with the initial response to the virus.
In Scotland, for example, First Minister Nicola Sturgeon asserted that mandatory mask rules could remain in place for years.

As we document in the video below, while the pandemic may be coming to an end, the conversation about the devastating and continued impact of lockdown restrictions should definitely not cease.

View: https://youtu.be/RAUOM5V2IYE
9:01 min
 

marsh

On TB every waking moment

Large, Peer-Reviewed Research Study Proves Ivermectin Works Against COVID-19

MONDAY, JAN 24, 2022 - 11:50 PM
Via FLCCC Alliance,

The results are in from the world’s largest study of ivermectin for COVID-19.


Brazil has had over 23 million cases of COVID-19 since the pandemic began, with a 97% recovery rate.

Researchers in Brazil found that regular use of ivermectin as a prophylactic agent was associated with significantly reduced COVID-19 infection, hospitalization and mortality rates.

The study was conducted in Itajaí, a port city in the state of Santa Catarina, between July and December 2020. Study authors include FLCCC physicians Dr. Flavio Cadegiani and Dr. Pierre Kory. Lead author Dr. Lucy Kerr was approached by the mayor of Itajaí, after the city began to experience a severe outbreak of COVID.

The entire population of Itajaí was invited to participate in the program, which involved a medical visit to compile baseline, personal, demographic, and medical information. In the absence of contraindications, ivermectin was offered as a preventative treatment, to be taken for two consecutive days every 15 days at a dose of 0.2 mg/kg/day.

Of the 223,128 citizens of Itajaí considered for the study, a total of 159,561 subjects elected to participate: over 70% opted to take ivermectin, and 23% chose not to.

Reduced infection and hospitalization rates
The study found a 44% reduction in COVID-19 infection rate in favor of the group that took ivermectin (3.5% versus 8.2%).

In cases where a participating citizen of Itajaí became ill with COVID-19, they were recommended not to use ivermectin or any other medication in early outpatient treatment. Of those who did become infected, two equal-sized, highly matched groups (one that used ivermectin as a prophylaxis and one that did not) were compared. The regular use of preventative ivermectin led to a 68% reduction in COVID-19 mortality (0.8% versus 2.6%), and a 56% reduction in hospitalization rate (1.6% versus 3.3%).

The regular use of preventative ivermectin led to a reduction in COVID-19 infection, hospitalization and mortality.
Study methods

Since vaccines were not available at the time, and few prophylactic alternatives existed in the absence of vaccines, Itajaí initiated a population-wide government program for COVID-19 prophylaxis. This was a prospective observational study that allowed subjects to self-select between treatment vs. non-treatment. The use of ivermectin was optional and based on patients’ preferences, given its benefits as a preventative agent was unproven.

To ensure the safety of the population, a computer program was developed to compile and maintain all relevant demographic and clinical data. All subjects were weighed to be able to accurately calculate the correct dose of ivermectin. In addition, a brief medical evaluation was conducted to record past medical history, comorbidities, use of medications and contraindications to drugs.

The following variables were analyzed and adjusted as confounding factors or used for balancing and matching groups for propensity score matching:
  • Age
  • Sex
  • Previous diseases (myocardial infarction and stroke)
  • Pre-existing comorbidities (type 2 diabetes, asthma, chronic obstructive pulmonary disease, hypertension, dyslipidemia, cardiovascular diseases, cancer [any type], and other pulmonary diseases)
  • Smoking
Patients who presented signs or the diagnosis of COVID-19 before July 7, 2020, were excluded from the sample. Other exclusion criteria included contraindications to ivermectin and age (subjects below 18 years of age were excluded).

During the study, subjects who were diagnosed with COVID-19 underwent a specific medical visit to assess clinical manifestations and disease severity. All subjects with symptoms were recommended not to use ivermectin, nitazoxanide, hydroxychloroquine, spironolactone, or any other drug claimed to be effective against COVID-19. The city did not provide or support any specific pharmacological outpatient treatment for subjects infected with COVID-19.

Intriguing findings
Interestingly, the group who self-selected to take ivermectin was older and had more comorbidities than the group who opted for no treatment. These results show that prophylactic ivermectin may be a mitigating factor in groups with higher risk of morbidity.


The results show prophylactic ivermectin may be a mitigating factor for high-risk groups.

The belief that preventative and early treatment therapies would cause people to relax their caution of remaining socially distanced, leading to more COVID-19-related infections, is not supported here.

The data demonstrate that using preventative ivermectin significantly lowers the infection rate, and that benefits outweigh the speculated increased risk of changes in social behaviors.
 

marsh

On TB every waking moment

Insurance Companies Note Jump In Death Payouts Amid 40% Rise Among Prime-Age Americans

TUESDAY, JAN 25, 2022 - 11:15 PM
Authored by Conan Milner via The Epoch Times (emphasis ours)

Insurance companies are reporting a jump in death payouts due to a dramatic rise in the number of deaths. The rise in the death rate is being corroborated by death certificate data from the Centers for Disease Control and Prevention (CDC).


More people are dying at younger ages and it's not because of COVID-19. But it isn't the government making a fuss about it, it's life insurance companies.(IR Stone/Shutterstock)


The death rate is up by 40 percent from pre-pandemic levels according to Scott Davison, chief executive of OneAmerica, a major insurance company based in Indianapolis. During an online news conference on Dec. 30, 2021, Davison said the change was unprecedented.

We are seeing, right now, the highest death rates we have seen in the history of this business,” he said.

OneAmerica sells life insurance to employers nationwide, and similar figures are found throughout the industry.

“The data is consistent across every player in that business,” Davison said. “And what we saw just in the third quarter—we’re seeing it continue into the fourth quarter—is that death rates are up 40 percent over what they were pre-pandemic. Just to give you an idea of how bad that is, a three-sigma or a one-in-200-year catastrophe would be a 10 percent increase over pre-pandemic. So 40 percent is just unheard of.”

This 40 percent figure doesn’t represent folks dying of old age, but is instead a reflection of deaths in working-age adults, aged 18 to 65. However, what’s responsible for the alarming spike in fatalities in this age group isn’t clear.

With all of the concern about COVID-19 lately, the contagion seems a likely choice. But according to Davison, something else is at play. He said the data coming from insurance companies—entities in the business of paying out when people die—show that the deaths being reported as COVID-19 fatalities “greatly understate” the actual deaths from working age people hit by the pandemic, as most of the claims being filed aren’t being classified as COVID-19 deaths.

“It may not all be COVID on their death certificate, but deaths are up just huge, huge numbers,” he said.

Also taking part in the news conference was Brian Tabor, president of the Indiana Hospital Association. He also noted a dramatic rise in illness from a different perspective. Tabor said hospitals across Indiana were being flooded with patients “with many different conditions.”

In October 2021, The Times of India reported that health insurers saw a “huge surge in non-COVID claims,” with the head of interventional cardiology at a Mumbai, India, hospital noting a 40 percent increase in heart problems compared to the previous six to eight months.

Ever since COVID-19 hit, the world has been bracing itself for huge numbers. Most recently in a White House press briefing on Dec. 17, 2021, President Joe Biden warned that unvaccinated Americans can look forward to a “winter of severe illness and death for yourselves, your families, and the hospitals you may soon overwhelm.”

Still, such astronomical figures emerging all of a sudden are hard to fathom. The pandemic has worn on for nearly two years, and health officials have been keeping a close eye on the death count. What could account for such a dramatic jump at the end of 2021?

[ZH: Answering this question is Epoch's Petr Svab with an in-depth analysis - buckle up]

Americans have been dying at a significantly higher rate over the past two years or so, but the COVID-19 disease tells only part of the story. Among seniors, the pandemic could explain the increase in mortality more easily than among younger people, where there’s a gap requiring further explanation.

Overall, there appear to be three distinct patterns in the data based on age:
Among those of age 0 to 17, mortality remained virtually unchanged since 2019.

Among those who were 65 or older, mortality increased in 2020, dropped in the first half of 2021, coinciding with the proliferation of the COVID-19 vaccines, and then increased in the third quarter of 2021, coinciding with the emergence of the Delta variant, which appeared more resistant to the vaccines.

1643174442723.png

Among those aged 18 to 49, mortality rose dramatically in the first half of 2020, then somewhat plateaued before increasing again in the third quarter of 2021.

The 50 to 64 age group appears to be a mix of the latter two patterns.

COVID-19 Impact
The differences between age groups become more apparent when deaths involving COVID-19 are highlighted.

Under the age of 18, COVID-related deaths barely register when visualized.

1643174526057.png

For those aged 75 and older, the novel disease more than explains any increases in mortality. For those aged 65 to 74, deaths were on the rise long before the pandemic. Excluding the COVID deaths leaves increases slightly above the previous trend.

1643174557496.png

1643174604851.png
1643174635807.png

Among those aged 18 to 65, however, there emerges the opposite phenomenon—after exclusion of COVID deaths, a significant hike in mortality remains. The non-COVID increase appears more pronounced in the younger age groups and less in the older ones.

1643174676244.png

1643174710345.png

1643174755785.png

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There are several factors that would explain at least part of the excess deaths.

Part 1 of 2
 
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marsh

On TB every waking moment
Part 2 of 2

Drugs, Alcohol, Murder

Drug overdoses skyrocketed in 2020 with more than 20,000 more dying in the 18–64 age group than the year before. The Centers for Disease Control’s (CDC) preliminary data for the first half of 2021 indicates the trend even somewhat intensified.

There are several factors that would explain at least part of the excess deaths. Drugs, Alcohol, Murder Drug overdoses skyrocketed in 2020 with more than 20,000 more dying in the 18–64 age group than the year before. The Centers for Disease Control’s (CDC) preliminary data for the first half of 2021 indicates the trend even somewhat intensified.

1643175204354.png

Deaths involving alcohol—not just alcohol poisoning, but also those due to alcoholic cirrhosis of the liver and other alcohol-induced causes—have been on the rise in recent years, but the 2020 increase was particularly significant. Nearly 8,000 more died in 2020 than the year before in the 18–64 age group. The 2021 data is not yet available.

1643175235543.png

Homicide deaths increased nearly 30 percent from 2019 to 2020 in the 18–64 age group, accounting for nearly 4,000 excess deaths. Last year is shaping up to be similarly homicidal, based on CDC’s preliminary data for the first half of 2021.

1643175480821.png

With COVID-19 deaths excluded and assuming drug overdoses, alcohol, and homicide deaths continued in 2021 at a similar intensity as the year before, there was still about 50,000 excess deaths last year in the 18-64 age group.

Misclassified, Overwhelmed
The CDC and some experts argue that the excess deaths could be misclassified COVID-19 deaths as well as deaths due to lack of care because of hospitals overwhelmed with COVID patients. They point to the fact that about third of Americans die at home. Their death certificates would be probably written by attending physicians who may not test the patient for COVID-19.

The CDC issued guidance on June 15, 2020, that all people suspected of dying of COVID-19 should be tested post mortem, but it’s not clear to what degree medical practitioners are following through on it.

This explanation may be limited for several reasons.

Deaths at home indeed increased with the onset of the pandemic, from less than 32 percent in 2019 to more than 36 percent in June 2020. But then the rate dropped again, to less than 31 percent in December 2020. If people were forced to die at home because medical care wasn’t available to them, it doesn’t appear to have been widespread enough to explain the excess mortality gap.

The argument for misclassified COVID deaths usually assumes that the dying person was suffering from multiple ailments and the attending physician failed to note COVID-19 as at least a contributing factor. It’s not clear how often that applies to younger people who are generally healthier and among whom COVID-19 deaths are rarer and may stand out more.

Finally, the argument appears to use backward reasoning—assuming the excess deaths are caused by COVID-19 and then seeking supporting logic on how that could be.

Vaccines
There’s a growing group of doctors and researchers who point to the COVID-19 vaccines as a possible culprit in at least a part of the excess deaths last year. They usually point to several physiological mechanisms through which the vaccines could cause harm combined with known side effects as well as data from the Vaccine Adverse Event Reporting System (VAERS), a database of reports of health problems that have occurred after a vaccination and may or may not have been caused by it.

VAERS reports exploded with the introduction of the COVID-19 vaccines. By Jan. 7, there were over a million reports, including more than 21,000 deaths.

Previously, there would be about 40,000 reports and a few hundred deaths a year. They are largely filed by health care personnel, based on previous research.
The usual arguments against the VAERS data have been that it’s unverified and unreliable. Some researchers have pointed out, however, that the system isn’t meant to provide definitive answers, but rather early warnings. In their view, the reports have raised numerous red flags that haven’t been sufficiently investigated.

CDC Data Caveats
The latest detailed cause-of-death data available on the CDC website is for the year 2020. For 2021, CDC has been releasing some preliminary data bi-weekly, but cautions that it has a lag of 8 weeks or more as the death certificate data streams in from around the country. For this analysis, only data up until October has been used. For specific causes of death beyond COVID-19, pneumonia, and influenza, the CDC doesn’t break down the available 2021 data by age, limiting its usefulness for this analysis.

In addition, CDC’s COVID-19 mortality data that covers 2021 attributes to the virus all deaths where COVID-19 was marked on the death certificate, regardless whether it was listed as the underlying cause or as a contributing factor. Early in the pandemic, the CDC instructed medical practitioners to mark all deceased who had tested positive, and even those with COVID-like symptoms but who had not been tested, as deaths caused by COVID-19. Later in 2020, the guidance gradually changed. Untested cases were to be separated and COVID-19 was required to be at least a contributing factor to be listed on the death certificate.

In the second half of 2020, the last period with available death certificate data on this point, nearly 90 percent of deaths involving COVID-19 had the disease listed as the underlying cause of death rather than a contributing factor.

Some experts have also pointed to government policies as a possible culprit in some excess deaths. School closures and business lockdowns have led to both financial and psychological depression, some research and anecdotal reports indicate, which may have led to death in some cases. Suicide deaths, though, have been relatively stable between 2019 and June 2021, based on available data.

Death After COVID
There may be a more hidden health impact of COVID-19. A study published in December found that people hospitalized for COVID-19 had somewhere between two and three times the risk of dying in the following 12 months of something other than COVID-19 than those going to a doctor, but testing negative.

“This huge explosion of inflammation during a severe episode of COVID seems to be causing a lot of other problems,” said Arch Mainous, the lead author of the study and a vice chair for research in the Department of Community Health and Family Medicine at the University of Florida.

“It looks like there is an overall impact on your body from this biological insult,” he told The Epoch Times.

The study has several limitations. It included people only from one hospital system in Florida and as such may not fully apply to the entire U.S. population. Also, it controlled for comorbidities, but used the Charlson Comorbidity Index (CCI), which only includes 17 general factors that aren’t specific to COVID-19. It includes age as well as issues such as history of heart attack, stroke, cancer, AIDS, cirrhosis, kidney disease, and diabetes. Mainous acknowledged that the index may be less predictive in younger patients.

Finally, the studied population as a whole had on average a particularly high risk of dying. Of the more than 13,600 people included, over 2,600 died within a year—nearly 20 percent. For comparison, Americans of age 85 or higher have about 10 percent annual mortality.
 
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marsh

On TB every waking moment

CDC study suggests unboosted vaccines become worse than nothing against Omicron

Agency confirms "protection against infection wanes to something undetectable," while maintaining that "we do not see that the risk of infection is increased" after lapse of protective window.

Updated: January 25, 2022 - 10:55pm

Two-dose COVID-19 vaccines may after an initial protective window become less effective against symptomatic infection by the Omicron variant than not getting jabbed at all, according to little-noticed findings in a federal study of how well boosters performed against different variants.

The "adjusted odds ratio" crossed 1 for vaccinated versus unvaccinated individuals 7-10 months after vaccination, according to the "original investigation" by Atlanta-based CDC researchers, published in the Journal of the American Medical Association last week.

That means the vaccinated were more likely than the unvaccinated to have symptomatic Omicron infections beginning at about the time the former become eligible for boosters. When considering the upper bound of the 95% confidence interval, the disparity emerged two months earlier.

Pfizer's mRNA vaccine performed worse than Moderna's, the researchers wrote.

"The upper bound of the 95% CI was consistently greater than 1 starting at 3 months after second dose" for the former and six months for the latter.

File
CDC booster omicron JAMA screenshot.pdf

By contrast, the odds ratios for either vaccine never got close to 1 for the Delta variant, even for the upper bound.

Even as evidence of the short-lived efficacy of the COVID mRNA vaccines continues to mount, federal regulators stepped in Tuesday to block doctors from using monoclonal antibodies to treat COVID patients. The FDA on Monday revoked authorizations for two such treatments against Omicron infections, including the one used by then-President Trump, finding they were "highly unlikely to be active" against the now-dominant variant.

The little-noticed findings in the JAMA study were highlighted by law professor Todd Zywicki, whose natural immunity lawsuit prompted George Mason University to grant him a medical exemption from its vaccine mandate.

"Still more confirmation that Pfizer and Moderna's CEOs know what they are talking about when they state that 2 doses of vax provides insignificant (at best) protection against Omicron," Zywicki tweeted Tuesday.

Pfizer CEO Albert Bourla said earlier this month that its vaccine offers "limited if any" protection against Omicron, while Moderna's preliminary booster data showed "low neutralizing antibody levels" against the variant before boosting.

View: https://twitter.com/i/status/1480995190966046725
.39 min

Both have promised Omicron-specific vaccines this year. On Tuesday, Pfizer and its German partner BioNTech announced a clinical study of such a vaccine among healthy 18-55 year-olds.

Perhaps the most vaccinated country in the world, Israel, appears poised to double down on boosters after a government advisory committee recommended a fourth dose for all adults, the Associated Press reported Tuesday.

Nearly half its population has received at least one booster, and the government started offering a second booster last month to those over 60.

One Israeli study found increased antibodies but not further protection against Omicron in twice-boosted healthcare workers, while another found such elderly people were "three times more resistant to serious illness" than the single-boosted, the New York Post reported.

Omicron is "not just an incremental shift of a variant, as Delta was from Alpha, but a fundamentally different challenge," Zywicki wrote in an email. People can "pretend like the vaccines are still providing protection" simply because the variant is relatively milder.

'Not distinguishable from 0'
While the JAMA study emphasizes the benefits of boosters against Omicron relative to either not getting vaccinated or two doses, researchers conceded that "the higher odds ratios for Omicron suggest less protection for Omicron than for Delta" among the boosted.

They studied about 23,000 COVID cases, mostly Omicron, among adults who were tested Dec. 10-Jan. 1 by a "national pharmacy-based testing program."

Twice as many controls were used. (Omicron now accounts for nearly 100% of infections.)

Most of the tests were performed in the 25-44 age range, three-quarters were white, and a third "reported underlying health conditions."

Researchers only counted vaccinated individuals who received the two-dose series at least six months earlier, and boosted individuals who received the third jab at least six months after the second.

The adjusted odds ratio of symptomatic Omicron infection for boosted versus unvaccinated individuals was 0.33, and for boosted versus two-dose recipients, 0.34. That means three doses corresponded with an "estimated effectiveness" of 67% over no doses, and 66% over two doses.

1643176014914.png

The study confirms that "OVERALL vaccine efficacy is zero," Zywicki told Just the News: The first few months of protection "rapidly approaches zero" around the six-month mark and then goes negative for a few more months.

He said the JAMA study was the fourth to find "basically this same negative [vaccine efficacy] effect" that he documented in an Epoch Times op-ed on "original antigenic sin."

Zywicki highlighted research from Toronto, California and Denmark that found negative VE starting two to six months after vaccination. The California study was "slippery," he claimed, because "the authors appear to have simply arbitrarily set a floor of zero vaccine efficacy."

The law professor's "understanding of epidemiology measurement is inadequate," the California study's lead author, epidemiologist Hung Fu Tseng, wrote in an email. "[A]lthough the odds ratio can be over 1, and 1-OR could be negative, the VE (or it's confidence interval) can not be negative. There is no mathematical meaning of a negative percentage."

The CDC disputed Zywicki's interpretation of its JAMA study.

"We see that 2 doses vs. unvaccinated against symptomatic infection with Omicron wanes to a number that is not distinguishable from 0 (i.e., our estimates even when negative are not significantly different from 0)," spokesperson Kristen Nordlund wrote in an email.

"So protection against infection wanes to something undetectable, but we do not see that the risk of infection is increased," she said. Nordlund also said the adjusted odds ratios were "not distinguishable from each other" because their confidence intervals overlapped.

This response amazed Zywicki. "[T]he CDC is admitting that vaccine efficacy is indistinguishable from zero from omicron?" he wrote. "Yeah we are going to put people through the risk of adverse side effects for two shots of vaccine that they acknowledge is at best zero in six months?"
 

marsh

On TB every waking moment

You Vote: Is FDA monoclonals halt about public health or saving one-size-fits-all vax strategy? (Poll on website)

FDA says COVID-19 antibody drugs from Regeneron, Eli Lilly should no longer be used because don't work against Omicron variant.

Updated: January 25, 2022 - 4:38pm

The Food and Drug Administration on Monday revoked emergency authorization for COVID-19 antibody drugs made by Regeneron and Eli Lilly.

The FDA said it made the decision to halt use of the monoclonal antibody treatments because they don't work against the Omicron variant, which now accounts for nearly all new COVID-19 infections in the U.S.

Antibody treatment is not meant to be a substitute for COVID-19 vaccines, but it's similarly meant to prevent severe disease and death.

The FDA's announcement comes amid a growing number of questions about the efficacy and safety of COVID-19 vaccines.

Pfizer CEO Albert Bourla said recently his company's own vaccine provides "limited if any" protection against Omicron, while Bill Gates criticized the performance of COVID-19 vaccines. A CDC report from earlier this month found natural immunity from previously being infected is better protection against the virus than the vaccine.

One analysis of the government's Vaccine Adverse Events Reporting System, primarily used by healthcare professionals, claims that COVID vaccines have prompted more reports in a year than all other vaccines combined going back to 1990.

However, federal and state health officials say that vaccines and boosters can keep most patients from getting the most serious cases of COVID-19 leading to hospitalization and death and that serious vaccine reactions are fairly rare.
 
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marsh

On TB every waking moment

Senator Ron Johnson Vaccine hearing… Cancer numbers are exploding…
Posted by Kane on January 26, 2022 12:21 am

View: https://twitter.com/i/status/1485780364685557764
.24 min

Three important highlights from yesterday’s hearing.

View: https://twitter.com/i/status/1485700814643638275
1:43 min

View: https://youtu.be/Lt7QzetfRSQ
2:51 min
 

marsh

On TB every waking moment

Courts push back against COVID mandates as Americans' support for such measures dwindles

Biden administration has set tone nationwide for COVID-19 mandates, but in recent months the president’s approval on the issue has steadily dropped.

By Casey Harper
Updated: January 25, 2022 - 11:26pm

U.S. courts are handing losses to Democrat-led COVID-19 polices around the nation, from federal to state rulings, as polling shows Americans are souring on the Biden administration’s approach to the pandemic.

New York Judge Thomas Rademaker threw out Gov. Kathy Hochul’s mask mandate this week, blocking the Democratic governor’s order for certain businesses.

At the same time, Texas Judge Jeffrey Brown granted an injunction to block the Biden administration’s vaccine mandate for federal employees and contractors.

Brown said the case in question considers whether the president can "with the stroke of a pen and without the input of Congress, require millions of federal employees to undergo a medical procedure as a condition of their employment.

“That, under the current state of the law as currently expressed by the Supreme Court, is a bridge too far,” he added.

Brown’s injunction comes just days after the U.S. Supreme Court blocked Biden’s federal vaccine mandate for private sector employers with at least 100 workers
The Supreme Court ruled in a 6-3 vote against that mandate, writing that the president does not have the authority to give the Occupational Safety and Health Administration (OSHA) the power to implement an economy-wide federal mandate of that kind.

On Tuesday, OSHA officially withdrew the rule.

Battles like this have played out at the state and local level around the country. In Utah, the state legislature enacted a measure last week to overturn mask mandates in Salt Lake and Summit counties.

The Biden administration has set the tone nationwide for COVID-19 policies and mandates, but in recent months the president’s approval on the issue has steadily dropped.

Polling released by Quinnipiac earlier this month reported Biden’s approval rating at a low of 33%.

“Americans give President Joe Biden a negative 33–53 percent job approval rating, while 13 percent did not offer an opinion,” Quinnipiac said. “In November 2021, Americans gave Biden a negative 36–53 percent job approval rating with 10 percent not offering an opinion.”

A major driver of that decline has been a decrease in support for Biden’s work on the coronavirus. According to the Quinnipiac poll, only 39% of those surveyed approved of Biden’s work on the pandemic, while 55% disapprove.

Recent polling also shows Americans have become less concerned about the virus over time, which may be weakening their support for more aggressive COVID-19 mandates.

The Associated Press-NORC Center for Public Affairs Research released new polling this month that showed only 37% of surveyed Americans list COVID-19 as one of their top five concerns that government should work on. Meanwhile, 68% of those surveyed pointed to an economic concern as an issue the government should be focused on.

Other groups are hoping the shift in public opinion, and particularly the court losses, provide new hope for their efforts.

A group of Navy SEALs that were denied religious exemptions to the vaccine have filed a lawsuit against the Biden administration. U.S. Department of Defense Secretary Lloyd Austin announced last year all service members must be vaccinated or face discharge.

Earlier this month, a federal judge issued an injunction in their case preventing the Navy from taking action against the service members until their case is resolved.

The Navy SEALS argue their exemption requests were not given fair consideration. On the heels of the recent Supreme Court ruling, they amended their lawsuit to be a class action case that includes “all U.S. Navy personnel who have requested a religious accommodation from the Navy’s vaccine mandate.”

“Our clients are boldly leading the fight against the vaccine mandate, but no service member should face discipline or punishment for following their faith,” said Mike Berry, General Counsel for First Liberty Institute, the group representing the Navy SEALs. “The fact that the military continues to demonstrate hostility to anyone who expresses religious objection to the vaccine mandate shows that the Biden Administration does not care about religious freedom. The lawsuit seeks to protect as many service members as possible from further punishment. We have to put a stop to this before any more harm is done to our national security.”
 

marsh

On TB every waking moment

Military Vaccines Adverse Reactions

Bombshell Cover-Up: Cancer Diagnoses in the Military Rose Over THREE-FOLD Since Jabs Were Introduced

By J.D. Rucker • Jan. 25, 2022

Yesterday’s “COVID-19: A Second Opinion” panel hosted in Washington D.C. by Senator Ron Johnson exposed bombshell after bombshell as fresh data keeps pouring in that shows the Covid-19 “vaccines” are neither safe nor effective.

Doctors from across the spectrum spoke up about what they’re seeing on the ground while other expert panelists exposed damning data demonstrating not only a huge medical problem, but also a coordinated cover-up of the evil deeds being perpetrated by members of our own government.

Conservative commentator Daniel Horowitz from The Blaze posted a follow-up bombshell of information he received from one of the panelists, attorney Thomas Renz:
I can share with you from attorney Thomas Renz that the number of cancer diagnoses in the military’s DMED system went from a 5-year average (2016-2020) of 38,700 per year to 114,645 in the first 11 months of 2021. This is a predominately young population.

Unlike VAERS where the naysayers can suggest that anyone can submit, this is only by military doctors and quantifies every single ICD code in the military for tri care billing of Humana. This is the ultimate defined and finite population with excellent surveillance.
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He also posted a video of Renz at the panel explaining some of the other mind-blowing data he had accumulated:

The video of Renz is here. I know 2 of the 3 cited whistleblowers. Their credentials are impeccable. Lt. Col. Chambers is one of the only Green Beret doctors in the military. Actually i got that wrong. One of the whitsleblowers just told me it was through October, not November. So this is 10 months of data off the chart vs. prior 12 month years!
One of the biggest takeaways here is that the data is beyond reproach and widely accessibly by the DoD, CDC, FDA, and across the Biden-Harris regime. In other words, they are all very well aware that the jabs are almost certainly causing an untenable increase in cancer in otherwise young and healthy military-age Americans and they’re keeping that information away from the people.

View: https://twitter.com/i/status/1485695818996854788
2:20 min


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The testimony that Renz delivered should be enough to compel our government to immediately halt the vaccine push, reevaluate the data that they have, and release it all to the public for independent scrutiny. They won’t do this, of course, because they have a universal vaccination agenda that they will not willingly stop. It will take a concerted effort by patriots to share this data and expose the powers-that-be for what they’re trying to do to the people.

“We have substantial data showing that we saw, for example, miscarriages increasing by 300% over the five-year average, almost.,” Renz said. “We saw almost 300% increase in cancer over the five-year average.”

This is crucial information for the entire population to have, but what he revealed next should concern us about the state of our military readiness.

“We saw — this one’s amazing — neurological. So, neurological issues which would affect our pilots, over 1000% increase. 1000,” he said.

Senator Johnson had to interrupt to reiterate what these numbers mean from a different angle. “Ten times,” he said. “That’s ten times the rate.”

Renz continued, “82,000 per year to 863,000 in one year. Our soldiers are being experimented on, injured, and sometimes possibly killed.”

Having Senator Johnson and the brave Americans on his panel speaking out is an important step, but the information will be swept under the rug if we fail to amplify the message as loudly as we can.
 

Large, Peer-Reviewed Research Study Proves Ivermectin Works Against COVID-19

MONDAY, JAN 24, 2022 - 11:50 PM
Via FLCCC Alliance,

The results are in from the world’s largest study of ivermectin for COVID-19.


Brazil has had over 23 million cases of COVID-19 since the pandemic began, with a 97% recovery rate.

Researchers in Brazil found that regular use of ivermectin as a prophylactic agent was associated with significantly reduced COVID-19 infection, hospitalization and mortality rates.

The study was conducted in Itajaí, a port city in the state of Santa Catarina, between July and December 2020. Study authors include FLCCC physicians Dr. Flavio Cadegiani and Dr. Pierre Kory. Lead author Dr. Lucy Kerr was approached by the mayor of Itajaí, after the city began to experience a severe outbreak of COVID.

The entire population of Itajaí was invited to participate in the program, which involved a medical visit to compile baseline, personal, demographic, and medical information. In the absence of contraindications, ivermectin was offered as a preventative treatment, to be taken for two consecutive days every 15 days at a dose of 0.2 mg/kg/day.

Of the 223,128 citizens of Itajaí considered for the study, a total of 159,561 subjects elected to participate: over 70% opted to take ivermectin, and 23% chose not to.

Reduced infection and hospitalization rates
The study found a 44% reduction in COVID-19 infection rate in favor of the group that took ivermectin (3.5% versus 8.2%).

In cases where a participating citizen of Itajaí became ill with COVID-19, they were recommended not to use ivermectin or any other medication in early outpatient treatment. Of those who did become infected, two equal-sized, highly matched groups (one that used ivermectin as a prophylaxis and one that did not) were compared. The regular use of preventative ivermectin led to a 68% reduction in COVID-19 mortality (0.8% versus 2.6%), and a 56% reduction in hospitalization rate (1.6% versus 3.3%).

The regular use of preventative ivermectin led to a reduction in COVID-19 infection, hospitalization and mortality.
Study methods

Since vaccines were not available at the time, and few prophylactic alternatives existed in the absence of vaccines, Itajaí initiated a population-wide government program for COVID-19 prophylaxis. This was a prospective observational study that allowed subjects to self-select between treatment vs. non-treatment. The use of ivermectin was optional and based on patients’ preferences, given its benefits as a preventative agent was unproven.

To ensure the safety of the population, a computer program was developed to compile and maintain all relevant demographic and clinical data. All subjects were weighed to be able to accurately calculate the correct dose of ivermectin. In addition, a brief medical evaluation was conducted to record past medical history, comorbidities, use of medications and contraindications to drugs.

The following variables were analyzed and adjusted as confounding factors or used for balancing and matching groups for propensity score matching:
  • Age
  • Sex
  • Previous diseases (myocardial infarction and stroke)
  • Pre-existing comorbidities (type 2 diabetes, asthma, chronic obstructive pulmonary disease, hypertension, dyslipidemia, cardiovascular diseases, cancer [any type], and other pulmonary diseases)
  • Smoking
Patients who presented signs or the diagnosis of COVID-19 before July 7, 2020, were excluded from the sample. Other exclusion criteria included contraindications to ivermectin and age (subjects below 18 years of age were excluded).

During the study, subjects who were diagnosed with COVID-19 underwent a specific medical visit to assess clinical manifestations and disease severity. All subjects with symptoms were recommended not to use ivermectin, nitazoxanide, hydroxychloroquine, spironolactone, or any other drug claimed to be effective against COVID-19. The city did not provide or support any specific pharmacological outpatient treatment for subjects infected with COVID-19.

Intriguing findings
Interestingly, the group who self-selected to take ivermectin was older and had more comorbidities than the group who opted for no treatment. These results show that prophylactic ivermectin may be a mitigating factor in groups with higher risk of morbidity.


The results show prophylactic ivermectin may be a mitigating factor for high-risk groups.

The belief that preventative and early treatment therapies would cause people to relax their caution of remaining socially distanced, leading to more COVID-19-related infections, is not supported here.

The data demonstrate that using preventative ivermectin significantly lowers the infection rate, and that benefits outweigh the speculated increased risk of changes in social behaviors.
Didn’t we just see a hit piece from business insider or something claiming IVM was a bust in Brazil?
 
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marsh

On TB every waking moment

FDA Suddenly Pulls Monoclonal Antibody Treatment EUAs: ‘They are Not a Substitute for Vaccination’

January 25, 2022
by Kyle Becker
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Written by Kyle Becker

The Food and Drug Administration suddenly rescinded the Emergency Use Authorization (EUAs) for a number of monoclonal antibody treatments that have been used for early treatment of Covid-19.

The Florida Department of Health made the announcement about the FDA’s “abrupt decision” to pull the EUAs for bamlanivimab/etesevimab as well as Regeneron. The decision has led to the Florida health department closing its monoclonal antibody sites statewide.

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“This evening, without any advanced notice, the US Food and Drug Administration (FDA) revised the Emergency Use Authorization (EUA) for bamlanivimad/etesevimab and REGEN-COV,” Florida Health announced. “The revised EUAs do not allow providers to administer these treatments within the United States.”

The Florida Health Department informed patients that their appointments for the Covid-19 treatment have been canceled. DeSantis has set up infusion sites in five counties: Palm Beach, Broward, Miami-Dade, Duval, and Seminole.

“Florida disagrees with the decision that blocks access to any available treatments in the absence of clinical evidence,” the announcement continued. “To date, such clinical evidence has not been provided by the FDA,” it added.
Gov. Ron DeSantis demanded the Biden administration reverse “its sudden and reckless decision” in a statement.

“Without a shred of clinical data to support this action, Biden has forced trained medical professionals to choose between treating their patients or breaking the law,” DeSantis said. “This indefensible edict takes treatment out of the hands of medical professionals and will cost some Americans their lives. There are real-world implications to Biden’s medical authoritarianism – Americans’ access to treatments is now subject to the whims of a failing president.”

Florida’s surgeon general Joseph A. Ladapo also responded to the FDA decision.

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“After [Health & Human Services] avoided communication with [the Florida Health Department]regarding statewide allocations, without any warning, [the FDA] suspended the use of multiple MABs treatments,” Dr. Ladapo stated. “Such decisions should be made based on clinical data – which the FDA has not provided.”

The National Institute of Health on January 19 revised its guidelines for Covid-19 drugs, including monoclonal antibodies. A January 25 release provided an overview of these changes.

“The Panel has updated this statement to address the fact that the B.1.1.529 (Omicron) variant of concern (VOC) is now the dominant SARS-CoV-2 variant in the United States,” NIH said. “Because the anti-SARS CoV-2 monoclonal antibodies (mAbs) bamlanivimab plus etesevimab and casirivimab plus imdevimab are predicted to have markedly reduced activities against this VOC, and because real-time testing to identify rare, non-Omicron variants is not routinely available, the Panel recommends against the use of these anti-SARS-CoV-2 mAbs (AIII).”

In mid-December, German researchers found in a pre-print study that the monoclonal antibody treatments “lose most of their effectiveness” against the Omicron variant.

“German researchers have found that COVID-19 therapies developed by Eli Lilly and Regeneron lose most of their effectiveness when exposed in laboratory tests to the Omicron variant of coronavirus, likely reducing treatment options if the new variant prevails,” Reuters earlier reported.

The FDA said it could reauthorize the EUAs if the two drugs prove to be effective against future variants or if they are updated to target Omicron.

“Just like vaccines will have to adapt, we’re probably going to have to constantly adapt our monoclonals,” Regeneron CEO Len Schleifer said in December.

The CDC and FDA have argued that monoclonal antibody treatments are not a substitute for vaccination and are generally reserved for vulnerable people, including seniors, transplant recipients and those with serious pre-existing health conditions, such as diabetes and heart disease.

During the Delta variant wave in late summer and early fall, demand soared for monoclonal antibodies. In late December, HHS announced it was pausing the distribution of Regen-CoV treatment and Eli Lilly’s bamlanivimab and etesevimab treatments, citing Omicron as the rationale. The Biden administration initially resumed distribution after Republican governors, including Florida Govt. DeSantis, argued that the treatments were helping some omicron patients.

The FDA is now touting alternate therapies for early Covid treatment, including two recently approved antiviral pills from Pfizer and Merck, which it has begun shipping to states.

Former President Donald Trump had received Regeneron’s antibody combination after he tested positive for Covid-19 in July 2020. Donald Trump attributed much of his recovery to Regeneron, which he said helped him feel better “immediately.”

“But I spent four days there, and I went in,” Trump said about Walter Reed hospital. “I wasn’t feeling so hot. And within a very short period of time, they gave me Regeneron. It’s called Regeneron. And other things too, but I think this was the key. But they gave me Regeneron, and it was, like, unbelievable. I felt good immediately. I felt as good three days ago as I do now. So I just want to say, we have Regeneron.”

“We have a very similar drug from Eli Lilly, and they’re coming out, and we’re trying to get them on an emergency basis,” he said. “We’ve authorized it. I’ve authorized it. And if you’re in the hospital and you’re feeling really bad, I think we’re going to work it so that you get them and you’re going to get them free. And especially if you’re a senior, we’re going to get you in there quick. We have hundreds of thousands of doses that are just about ready. I have emergency use authorization all set, and we got to get it signed now.”

The FDA’s recent decision to pull the emergency use authorization for the treatments drew additional rebuke from DeSantis.

“Without a shred of clinical data to support this action, Biden has forced trained medical professionals to choose between treating their patients or breaking the law,” DeSantis said. “There are real-world implications to Biden’s medical authoritarianism – Americans’ access to treatments is now subject to the whims of a failing president.”

Florida’s surgeon general Joseph Ladapo argued that the Biden administration’s abrupt decision was being made for political reasons.

“In our field of medicine, when someone comes to you seeking a treatment that could save their life, it is essential to have treatment options to ensure health care providers can make the best decisions for their patients,” Ladapo said. “The Federal Government has failed to adequately provide the United States with adequate outpatient treatment options for COVID-19. Now, they are scrambling to cover up a failure to deliver on a promise to ‘shut down the virus.’”
 

marsh

On TB every waking moment

Driver who stopped to help when truck carrying 100 lab monkeys crashed in Pennsylvania and put her hand in one of the cages says she now has a cough and pink eye after one of the macaques HISSED in her face
  • Woman who stopped to help monkeys in truck crash is now feeling unwell
  • Michelle Fallon, from Danville near Scranton, was directly behind the truck
  • Fallon said the day following the accident she developed a cough and pink-eye
  • She has begun a course of antiviral drugs and treatment to prevent rabies
  • The last of the four escaped monkeys was accounted for by late Saturday
  • One of the cynomolgus macaques, which are also known as crab-eating or long-tailed macaques, was found in a tree
  • Pennsylvania residents had been warned not to engage a crab-eating macaque that escaped from a truck carrying 100 of them to a lab
  • Crates with live monkeys inside were strewn across State Route 54 in Danville, 130 miles from Philadelphia, after the crash
  • A witness said he thought he saw a cat run across the road before making the shocking realization that it was actually a fleeing primate
By JAMES GORDON FOR DAILYMAIL.COM
PUBLISHED: 02:33 EST, 25 January 2022 | UPDATED: 08:59 EST, 25 January 2022

A woman who stopped to help after a truck carrying 100 lab monkeys crashed in Pennsylvania fears she's caught an illness after one of the macaques hissed in her face, leaving her with pink eye symptoms.

Michelle Fallon, from Danville near Scranton, was driving directly behind the vehicle when it crashed, throwing animal crates all over the highway and smashing some to pieces. Three of the macaques escaped and went on the run, but all have since been captured and humanely euthanized. All of the other monkeys - who'd arrived in the US from Mauritius that morning, and were en route to a lab, have been accounted for.

Fallon has now had a rabies shot, and wrote about the symptoms she has since suffered on Facebook - and also told PA Homepage that she'd developed symptoms of pink eye - an inflammation or infection of the eye ball.

She said: 'I was close to the monkeys, I touched the crates, I walked through their feces so I was very close. So I called (a helpline) to inquire, you know, was I safe?

'Because the monkey did hiss at me and there were feces around, and I did have an open cut, they just want to be precautious.'

Fallon said she got out to help both the driver and the animals in their cages, initially believing them to be cats. When she approached and put her hand on the cage, she says the monkey hissed at her.

The day following the accident, Fallon suddenly developed a cough and pink eye, which became so bad that she had to visit the emergency room at Geisinger Medical Center in Danville.

Michele Fallon, who was exposed to the monkeys on Friday after the crash said she is experiencing some side effects in her eye and has begun a course of preventative rabies treatment


Michele Fallon, who was exposed to the monkeys on Friday after the crash said she is experiencing some side effects in her eye and has begun a course of preventative rabies treatment

Fallon wrote of her experience on her Facebook page


Fallon wrote of her experience on her Facebook page

Pictured: the last of the four monkeys to be captured after the trailer they were in crashed into a dump truck on a Pennsylvania highway on Friday


Pictured: the last of the four monkeys to be captured after the trailer they were in crashed into a dump truck on a Pennsylvania highway on Friday

Crates holding live monkeys are collected next to the trailer they were being transported in along state Route 54 at the intersection with Interstate 80 near Danville, Pennsylvania on Friday  after a pickup pulling the trailer carrying the monkeys was hit by a dump truck


Crates holding live monkeys are collected next to the trailer they were being transported in along state Route 54 at the intersection with Interstate 80 near Danville, Pennsylvania on Friday after a pickup pulling the trailer carrying the monkeys was hit by a dump truck

https://videos.dailymail.co.uk/prev...198747530/636x382_MP4_5245252496198747530.mp4 1:28 min

Truck transporting 100 monkeys to a lab crashes in Pennsylvania

What is the monkey Herpes B virus

Contracting the B virus is extremely rare, but it can lead to severe brain damage or death if you do not get treatment immediately.

People typically get infected with B virus if they are bitten or scratched by an infected macaque monkey, or have contact with the monkey's eyes, nose, or mouth.

You may develop small blisters in the wound or area on your body that had contact with the monkey.

There are no known vaccines to protect against a B virus infection, and so people are urged not to touch or feed monkeys.

Only one case has been documented of an infected person spreading B virus to another person.

Source: CDC

Infectious disease doctors gave her the first of four rabies injections together with some anti-viral drugs.

She said on Facebook that she was monitoring for symptoms of rabies and monkey herpes virus B.

'What a day! I tried to help out at an accident and was told there were cats in the crates. So I went over to pet them only to find out it's monkeys. Then I noticed that there was three in each, with some completely broken, so I knew four had got away,' Fallon wrote of her experience on her Facebook page.

'I came home to go to bed and my aunt ran into a news crew and she found out not to get too close to the monkey. Well, I tried to pet one. I touched the crates and walked in poop. I was told meet the police at the scene to talk about exposure', she explained.

'I spoke with the police and a woman from the CDC I am getting a letter and I'm very low risk for I don't know what yet. But my symptoms are covid symptoms. Like seriously. A day from hell!'

Fallon has been told to keep a close eye on her health for the next month in case she develops any infectious disease as a result of being so close to them.

The test monkeys were on their way to a laboratory in Florida when the truck crashed into a garbage truck.

Fallon said that she spoke with the pickup driver and a passenger directly after the crash.

The driver appeared to be disoriented, and the passenger thought he might have injured his legs, she said.

The pickup was heading west on I-80 when it got off at the Danville exit and then immediately tried to get back on, driving across the other lane.

Fallon explained how she was behind the pickup when it was hit on the passenger side by the dump truck, tearing off the front panel of the trailer and sending more than a dozen crates tumbling out.

She and another motorist who stopped to help were standing near the scene when the other driver said he thought he saw a cat run across the road, Fallon said.

The CDC has now written to Fallon informing her to watch for any further symptoms in the next month


The CDC has now written to Fallon informing her to watch for any further symptoms in the next month

Crates holding live monkeys are pictured scattered across the westbound lanes of state Route 54 on Friday at the junction with Interstate 80 near Danville, Pennsylvania


Crates holding live monkeys are pictured scattered across the westbound lanes of state Route 54 on Friday at the junction with Interstate 80 near Danville, Pennsylvania

State police had urged people not to look for or capture the crab-eating macaque monkey following the crash on a a highway in Danville, about 130 miles from Philadelphia


State police had urged people not to look for or capture the crab-eating macaque monkey following the crash on a a highway in Danville, about 130 miles from Philadelphia

Fallon peeked into a crate and saw a small monkey looking back at her, she told the newspaper.

'They're monkeys,' she told the other motorist.

Jamie Labar, who was working the front desk of a nearby Super 8, said she initially thought it was a joke when someone told her of the accident.

All of the escaped monkeys were accounted for by Saturday after the Pennsylvania Game Commission and other agencies launched a search for it, amid frigid weather.

Three of the escaped lab monkeys were dead after being euthanized.

One of the cynomolgus macaques, which are also known as crab-eating or long-tailed macaques, was found in a tree, and three shots were later heard, WNEP reported.

State police had urged people not to look for or capture the cynomolgus macaque monkey following the crash on a State Route 54 near an Interstate 80 exit in Danville, about 130 miles from Philadelphia.

53337915-10438357-image-m-66_1643095789824.jpg


One of the monkeys (pictured) was found in a tree, and three shots were later heard, WNEP reported

PETA reminded residents after the crash that 'there is no way to ensure that monkeys are virus-free.' Pictured, one of the monkeys was found hiding in a tree


PETA reminded residents after the crash that 'there is no way to ensure that monkeys are virus-free.' Pictured, one of the monkeys was found hiding in a tree

'Anyone who sees or locates the monkey is asked not to approach, attempt to catch, or come in contact with the monkey. Please call 911 immediately,' troopers had tweeted prior to locating the primates.

Trooper Lauren Lesher had said the concern was 'due to it not being a domesticated animal and them being in an unknown territory. It is hard to say how they would react to a human approaching them.'

The shipment of monkeys was en route to a CDC-approved quarantine facility after arriving Friday morning at New York's Kennedy Airport from Mauritius, the agency said.

Crates littered the road Friday as troopers searched for the monkeys, rifles in hand.

Meanwhile, Valley Township firefighters used thermal imaging to locate the animals, with a also assisting the recover effort.

The US Centers for Disease Control and Prevention (CDC) said the agency provided 'technical assistance' to state police.

The truck had been on its way to a lab at the time of the crash.

The location of the lab and the type of research for which the monkeys were destined weren't clear, but the cynomolgus monkeys are often used in medical studies.

The Pennsylvania Game Commission and other agencies used a helicopter to search for it amid frigid weather


The Pennsylvania Game Commission and other agencies used a helicopter to search for it amid frigid weather

Crates littered the road Friday as troopers searched for monkeys, rifles in hand. Valley Township firefighters used thermal imaging to locate the animals, and a helicopter assisted


Crates littered the road Friday as troopers searched for monkeys, rifles in hand. Valley Township firefighters used thermal imaging to locate the animals, and a helicopter assisted

A 2015 paper posted on the website of the National Center for Biotechnology Information referred to them as the most widely used primate in preclinical toxicology studies.

Lesher said state police secured the scene for the Pennsylvania Department of Health and the U.S. Centers for Disease Control and Prevention.

Although macaque monkeys are cute, PETA reminded residents after the crash that 'there is no way to ensure that monkeys are virus-free,' noting that 'records show that monkeys in laboratories in the US have been found with tuberculosis, Chagas disease, cholera and MRSA.'

The monkey isn't just dangerous, it's expensive - crab-eating macaques can cost up to $10,000, according to The New York Times.

The monkeys, whose DNA is similar to that of humans, have been in high demand amid the COVID-19 pandemic, with some scientists calling for an emergency reserve of the test subjects similar to the country's stockpiles of oil and grain.

Those who believe they may have had contact with the monkeys are asked, per the CDC letter, to seek medical attention and contact Pennsylvania Department of Health at (717) 787-3350.

****
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Heliobas Disciple

TB Fanatic
(Canada)
https://citizenfreepress.com/breaking/the-unvaccinated-will-be-allowed-to-buy-milk-in-quebec/
The Unvaccinated will be allowed to buy milk in Quebec.
Supervised shopping is coming to Quebec. You will only be allowed to buy certain items.

In Quebec, they will now have someone from the store escort unvaxxed through big box stores to make sure they are only buying food or pharmacy items. I guess "according to the science" in Canada - you are only infectious in non-food aisles. If you're in a pharmacy line or in a food aisle, miraculously you aren't infectious/ sarcasm. This is life in the 21st Century. You couldn't write fiction this bad.

This is the video of the news report:
View: https://twitter.com/colin_korol/status/1485658340122259459

HD


ETA: for those who rightfully doubt that this could possibly be true, here is a link:

(fair use applies)

EXCERPT

[...]

Vaccine passports now required at large retailers

Starting today, some larger retailers stores in Quebec will require a vaccination passport for entry.

In a bid to persuade COVID-19 vaccine holdouts to get the jab, Quebec has expanded the vaccine mandate to include all businesses with surface areas of 1,500 square metres or more — with the exception of groceries and pharmacies.

The province's health ministry released a ministerial decree detailing the parameters of the new directive Sunday night.

For pharmacies located in big-box stores, such as Walmart or Costco, an unvaccinated person must be "accompanied at all times during his or her travels by an employee of the business, the pharmacy or any other person mandated by them for this purpose," the decree reads. This person may not purchase products other than those related to the pharmaceutical service they are receiving.

[...]
 
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marsh

On TB every waking moment

Why the Legacy Media Tried to Distract From and Dismiss Defeat the Mandates D.C.

By Jennifer Oliver O'Connell | Jan 24, 2022 10:30 PM ET

Screenshot-Defeat-the-Mandates-Livestream-on-CHD.TV_-730x0.jpg
Screenshot-Defeat the Mandates Livestream on CHD.TV

If you have opportunity, I would strongly recommend viewing the LiveStream of Sunday’s “Defeat the Mandates: An American Homecoming” Rally in Washington D.C. My colleague Nick Arama reported on the event, and gave an overview about those in attendance. LifeSite News did a lovely compilation of interviews with the attendees.

Rumble video 4:18 min

You could well say that America was fully represented: vaccinated, unvaccinated, Democrat, Republican, Independent, non-partisan, apolitical, white, Black, Latino, whatever label you want to apply, they were in full force, enthusiastic, and motivated. These Americans braved the 36 degree cold to hear the lineup of musical artists and speakers, and to make their voices heard. The comedian and satirist JP Sears moderated and introduced the speakers, which were the primary focus. But if anyone paid attention to the legacy media, it would appear that Robert F. Kennedy, Jr., whose Children’s Health Defense helped to organize the event, was their main focus with his “offensive” comparisons of the vaccine mandates to Nazi Germany and Anne Frank.

From the network searching for relevance (and ratings), CNN:
“Even in Hitler Germany (sic), you could, you could cross the Alps into Switzerland. You could hide in an attic, like Anne Frank did,” said Kennedy, a prominent anti-vaccine advocate, in a speech at the Lincoln Memorial. “I visited, in 1962, East Germany with my father and met people who had climbed the wall and escaped, so it was possible. Many died, true, but it was possible.”

Kennedy’s historically inaccurate anti-Semitic remark ignores the fact that Frank and some 6 million other Jews were murdered by Nazis. Frank, who was a teenager at the time, hid in an attic in the Netherlands, not Germany, before she was caught and was sent to a concentration camp, where she died.

The Auschwitz Memorial responded to Kennedy in a statement on Twitter, saying, “Exploiting of the tragedy of people who suffered, were humiliated, tortured & murdered by the totalitarian regime of Nazi Germany – including children like Anne Frank – in a debate about vaccines & limitations during global pandemic is a sad symptom of moral & intellectual decay.”

The son of former Attorney General and presidential candidate Robert F. Kennedy has a long history of spreading vaccine misinformation.

My how the long knives were drawn for less than a two-minute portion of Kennedy’s 25-minute speech. The majority of the media coverage fixated on Kennedy and only Kennedy, when he was one of a number of speakers that appeared at the event. The two hours and 50 minutes before Kennedy’s address are what really packed the punch, and what the legacy media wants to be ignored.

Dr. Peter McCullough effectively opened the event, with powerful statements on three critical circles:

“We have a circle of medical freedom,” McCullough said.

“You have the freedom. You and you alone have the autonomy overy your body. You have the freedom to determine what happens to your body. That is your sole possession. In many ways it’s the only thing you really have. That is your possession.

“That circle of medical freedom is inextricably linked to a circle of social freedom: and that social freedom includes your family, and your employment, and your faith, it involves your overall citizenry in any country that you reside, in any state that you reside. And that is inextricably linked to the circle of economic freedom. Medical freedom is linked to social and economic freedom.

“If we allow the circle of medical freedom to even be touched, let alone be broken, all the circles fracture. They all do, and they crumple. So the writing is on the wall, and the determination to preserve medical freedom is in your hands. It’s in your personal hands. It can’t be any more clear. This moment cannot be more decisive. So join me, and join these heroic doctors, and nurses, and others, and help bring America Home.”

Dr. Robert Malone, followed him, invoking St. Augustine in exposing the truth about the COVID and vaccine cover up.

“The truth is like a lion. You don’t have to defend it. Let it loose, it will defend itself,” Malone quoted.
Malone then talked about the risks in the vaccine that the government and pharmaceutical giants have attempted to hide to prevent people from making conscious and informed choices.

“If there is risk, there must be CHOICE,” he roared.
“This is the fundamental bedrock truth of modern bioethics. To deny this is to deny human dignity.”
However, it was the space in between these speakers that was extraordinary and riveting. Medical professionals: doctors, nurse practitioners, clinicians, took the stage to make their stand with their fellow Americans. Dr. Paul Marik, Dr. Pierre Kory, and Dr. Mary Talley Bowden, who had her hospital privileges at Houston Methodist Hospital suspended for allegedly spreading “misinformation” about COVID-19. Dr. Bowden resigned, and is now suing the medical corporation.

Dr. Paul Alexander called the pandemic what it is:

“Fraud from the beginning. Vaccine immunity can never, ever supersede your natural immunity, PERIOD,” he said.
“It is time for us to understand that we need to bring this pandemic to a close. We need to declare this pandemic emergency over.
“We cannot let these faceless technocrats and bureaucrats rule our lives.”

Dr. Aaron Kheriaty, who was fired from his position at the University of California Irvine for his stance against vaccine mandates laid it plain: “History is repeating. We must stop it.”

History is repeating. We must stop it. from Dave Tonnes on Vimeo. 2:17 min

The most heart wrenching and revealing portion of the event were the testimonials from the vaccine injured. People like Dr. Joel Wallskog, an orthopedic surgeon who on December 30, 2020, took his first Moderna shot, and soon after lost his mobility. Wallskog was diagnosed with transverse myelitis, a rare injury of the spinal cord. He can no longer practice medicine.

Then there is Kyle Warner, a professional mountain biker who was injured after getting his second shot of the Pfizer vaccine.

“Zero corporate liability. Zero backup plan. What could go wrong? Warner said.

“This is real. People are being harmed. People are losing their livelihoods and in some cases their lives. While the government and companies like Pfizer sit back and watch.”
These Americans represented the 12,500 (and counting) vaccine injured in the nation. REACT19, an organization created to bring awareness and assistance to those who have been vaccine injured introduced a powerful video called, “Silence,” to bring attention and recognition to the many who are suffering or have lost their lives after getting the jab.

View: https://youtu.be/UMCXFHNQDXI
3:13 min

The legacy media is doing its utmost to hold up a narrative that is rapidly falling apart. Better you ignore this event, or focus on one statement in one speech, than to face the truth of the damage done and their complicity in it.
 

marsh

On TB every waking moment
View: https://www.youtube.com/watch?v=2Zzo4SJopcY
25:14 min

The Case for Sunlight in COVID 19 Patients: Oxidative Stress

Jan 26, 2022


MedCram - Medical Lectures Explained CLEARLY


Roger Seheult, MD of MedCram presents the case for sunlight as a treatment for COVID-19. See all Dr. Seheult's videos at: https://www.medcram.com (This video was recorded on January 26, 2022) Roger Seheult, MD is the co-founder and lead professor at https://www.medcram.com He is Board Certified in Internal Medicine, Pulmonary Disease, Critical Care, and Sleep Medicine and an Associate Professor at the University of California, Riverside School of Medicine. LINKS / REFERENCES: Autumn COVID-19 surge dates in Europe correlated to latitudes, not to temperature-humidity, pointing to vitamin D as contributing factor (Nature) | https://www.nature.com/articles/s4159... SARS-CoV-2 positivity rates associated with circulating 25-hydroxyvitamin D levels (PLOS) | https://journals.plos.org/plosone/art... Influenza Deaths Per Week in the US (SAS) | https://sascommunities.github.io/grap... Hospitalizations (SBCPH) | https://covid19-sbcph.hub.arcgis.com/... Vitamin D Deficiency and Outcome of COVID-19 Patients (Nutrients) | https://pubmed.ncbi.nlm.nih.gov/32927... Melatonin and the Optics of the Human Body (Melatonin Research) | https://www.melatonin-research.net/in... Blood Clots & Strokes in COVID-19; ACE-2 Receptor; Oxidative Stress (MedCram) | https://youtu.be/22Bn8jsGI54 COVID-19 and Oxidative Stress (MedCram) | https://youtu.be/gzx8LH4Fjic Severe Glutathione Deficiency, Oxidative Stress and Oxidant Damage in Adults Hospitalized with COVID-19 (MDPI) | https://www.mdpi.com/2076-3921/11/1/50 DermatologyUltraviolet A radiation and COVID-19 deaths in the USA with replication studies in England and Italy (BJD) | https://onlinelibrary.wiley.com/doi/e... The Science of Near-Infrared Lighting: Fact or Fiction (IES) | https://www.ies.org/fires/the-science... Measure Guideline: Energy-Efficient Window Performance and Selection (USDE) | https://www.nrel.gov/docs/fy13osti/55...
 

marsh

On TB every waking moment

And Yet More Fragging
People who want to act like journalists need to behave responsibly.

“In the United States military, fragging (from fragmentation grenade) refers to the act of murdering members of the military, particularly commanders of a fighting squad. Additionally, the term can be applied to manipulating the chain of command in order to have an individual, or unit, deliberately killed by placing the personnel in harm's way, with the intended result being death. An example would be to order a soldier to perform a particularly hazardous task, and continue to repeat the order until the soldier met his demise. Originating among United States troops during the Vietnam War, the term was most commonly used to mean the assassination of an unpopular officer of one's own fighting unit. Such incidents have been documented in European military history back to the 18th century.
Current usage could apply to murder of any other member, enlisted or officer, and has nothing to do with rank. Initially, the killings were effected by means of a fragmentation grenade,[1] making it appear as though the killing had been accidental, or the result of combat action with the enemy, thereby obscuring the assassin's true intentions. The term now encompasses any means of deliberately and directly causing the death of fellow military members.”
From: Fragging
As if my life were not complicated enough, yesterday I received emails from colleagues in Spain and on Maui regarding a recent newsletter publication by an organization I had never heard of, “Health Freedom for Humanity” The email from Spain had been forwarded by my friend Dr. Geert Vanden Bossche, who lives in Belgium. Apparently this newsletter post has gone globally viral. The article was written by Jeff Witzeman (Instagram profile linked)



Here is the version of the hit piece text, forwarded to me from both Maui and Belgium, and put out by this mysterious organization:


From Jeff Witzeman's Health Freedom for Humanity newsletter:
In a shocking development, we are discovering that Dr. Robert Malone, viewed by so many as a hero for saying nobody should get the Pfizer and Moderna vaccines, is actually developing his OWN COVID VACCINE! And it allegedly has Darpa (graphene oxide) Hydrogel in it.
No mention of this vaccine was ever made on the Joe Rogan interview, bringing the question of conflict of interest. Malone also stated in the Rogan interview that he collaborated with the CIA on a project. (For more on Graphene Oxide Hydrogel read here.)
We had a lively discussion among the podcast team of HFFH whether we wanted to interview Malone and if that would have any value. Dr. Stanton Hom asked the question of where we draw the line with who we interview and I was fascinated by his answer. He said that anyone who is willing to admit the vaccine schedule for children (72) is evil or at the very least seriously off, is one of us and fair game for speaking on our platform. We are still inclusive and welcome all beliefs, but when it comes to our stage, that is where we have to draw a line.”
So, who is Stanton Hom?


He is a Chiropractor, who practices here

So, hoping to find out what the heck is going on here, I look for someone affiliated with this group that I have had contact with, and find Dr. Ben Tapper, another Chiropractor. I write to him, and receive the following reply:
“Hey Doc,
I am not on the board anymore. :/ I passed on the info to the board. I’m hopeful they will respond. I apologize this is happening. “
Then I reach out through my network to find out if anyone knows about this organization, and am put in touch with Mr. Alec Zeck, who self-identifies as Executive Director of “Health Freedom for Humanity”. Mr. Zeck calls me while I am having dinner with colleagues here in Nashville, TN, and gives me a series of excuses for how this happened but fails to take ownership and responsibility for the defamation and slander, and after I hear him explain that he is only 29 years old (as if that is an excuse), I hang up. When I called him this morning, as I am writing this article instead of enjoying a peaceful morning preparing for recording an interview with Candice Owens Show, he informed me that his organization will publish a retraction and apology later today.

But let’s be very clear, a retraction of the newsletter at this point will get read by a tiny, tiny fraction of the people who have seen this slanderous article - as it has literally gone global. The damage to my reputation is real.

So, lets walk through this “Shocking Development”, claim by claim:

Statement #1- “Dr. Robert Malone, viewed by so many as a hero for saying nobody should get the Pfizer and Moderna vaccines, is actually developing his OWN COVID VACCINE! “
I am not developing “my own vaccine.” The vaccine product (Relcovax) is being developed by Reliance Life Sciences, not me. I used to consult for Reliance. I no longer do. I have no ownership, stock, or any ongoing consulting or contractual relationship with Reliance at this point. This is a sub-unit vaccine, not a genetic vaccine. I was very glad (and honored) to assist, coach and mentor the Reliance Life Sciences when I was serving as a consultant. They are highly experienced and fully committed to developing safe and effective vaccines in full compliance with international and Indian government standards. Which is probably why this vaccine is still not in clinical testing at this point, despite briefing about two years into development. Of relevance is that the Indian national regulatory authority guidance for vaccine development and licensure is more rigorous than that of the FDA, consequent to the various prior transgressions of Merck Vaccines and the Bill and Melinda Gates Foundation when doing business in India.

This is not my vaccine, and never has been (below is a presentation at a vaccine conference about this vaccine).

The vaccine is being developed by Reliance Life Sciences. I used to consult for Reliance. I no longer do. I have no ownership, stock, or any ongoing consulting or contractual relationship with Reliance at this point. I was very glad (and honored) to assist, coach and mentor the Reliance Life Sciences when I was serving as a consultant. They are highly experienced and fully committed to developing safe and effective vaccines in full compliance with international and Indian government standards. Which is probably why this vaccine is still not in clinical testing at this point, despite briefing about two years into development. Of relevance is that the Indian national regulatory authority guidance for vaccine development and licensure is more rigorous than that of the FDA, consequent to the various prior transgressions of Merck Vaccines and the Bill and Melinda Gates Foundation when doing business in India.

This is not my vaccine, and never has been.
Statement #2- “it allegedly has Darpa (graphene oxide) Hydrogel in it”.
Hydrogel, and other alum-based adjuvants, are among the best characterized of the traditional adjuvants. DARPA had nothing to do with developing Alum or Alhydrogel adjuvants. Alhydrogel has nothing to do with Graphene Oxide. This “Relcovax” vaccine product using Alum + CpG for its adjuvant system. The vaccine candidate is designed to be a very low cost, traditional alternative to the genetic vaccines, and employs much more traditional methods than, say, the Novavax product.

This statement clearly demonstrates the profound ignorance of the author, and his willingness to use the same fearporn and hyperbole which I find so offensive in so many of the attack articles that seek to damage my reputation.
Statement #3- “No mention of this vaccine was ever made on the Joe Rogan interview, bringing the question of conflict of interest”
This is not my vaccine, I am not engaged as a consultant by Reliance, and I have no financial interests in this vaccine. Another example of the author and organization seeking to damage my reputation using classic yellow journalism smear tactics.
Statement #4- “Malone also stated in the Rogan interview that he collaborated with the CIA on a project. “
Another false statement designed to smear my reputation. I have co-published with Dr. Michael Callahan on manuscripts relating to the Zika virus. You can find those articles here. You can find information regarding Dr. Michael Callahan here.

I have not collaborated with the CIA. I do have a (currently inactive) secret DoD clearance. I have actively collaborated with USAMRIID, and I am proud of our work together repurposing drugs for Zika and Yellow Fever (which included ivermectin, Hydroxychloroquine, Niclosamide, Nitazoxanide, and many others).
Statement #5- “He said that anyone who is willing to admit the vaccine schedule for children (72) is evil or at the very least seriously off, is one of us and fair game for speaking on our platform. We are still inclusive and welcome all beliefs, but when it comes to our stage, that is where we have to draw a line.”’
I just do not know where to start with this word salad. Is Stanton Hom saying that I am evil or seriously off? On what basis? So, if I am able to interpret this correctly, the justification for not speaking to me prior to sending out this little nasty piece of work into the internet is that I am evil based on ???.

In conclusion, I regret having to take my morning to write this retort and apologize for having to send it into your inbox.

Now, there are the various attack articles written by hostile press outlets, and typically are composed by junior writers seeking five minutes of fame and pieces of silver by denigrating me (The Atlantic Monthly and Washington Post articles being among the most egregious). These mostly serve to illustrate the bias of the Atlantic (owned by a Biden megadonor and Bill Gates), and the Washington Post (owned by Biden megadonor Jeff Bezos).

And then there is the fragging, like this piece of work from “Jeff Witzeman's Health Freedom for Humanity newsletter” that I have discussed above.

What I run into, again and again, is frightened people who do not understand the science, and jump to conclusions about what they see as nefarious activities. In some ways, this is even more dangerous to the cause of truth and transparency, because it injects false issues into the discussion. This is not science, it is just paranoia.

So, please. If you have concerns about anything that I have said or done, or the technology I created or the scientific research that has been accomplished in my laboratory over the years, please do me a favor and contact me before you send some defamatory text out onto the internet to go internationally viral. In the interest of respect for integrity, human dignity, and community, if for no other reason.

And in the meantime, please do not hesitate to contact Alec Zeck, Stanton Hom, Jeff Witzeman and “Health Freedom for Humanity” and let them know what you think about all of this. And for any who know me personally and want to call Alec Zeck directly to get his take on this, please get in touch and I will gladly forward his V-card so that you can discuss your point of view directly with him.
 

marsh

On TB every waking moment

marsh

On TB every waking moment
View: https://www.youtube.com/watch?v=yy_5vyWq-Hs
10:42 min

Recordings of Possible Botched Administration of COVID Vax on Kids "Some people got the wrong one"

Jan 26, 2022

Project Veritas


Full report at http://ProjectVeritas.com New York Nurse Whistleblower Recordings Show Possible Botched Administration of COVID-19 Vaccine on Children: ‘Some People Got the Wrong One ’ • Medical supervisor admits “some people got the wrong one.”. • Nursing staff told to “YouTube it” when asking how to mix the COVID-19 Vaccine • Nursing staff on video: “wrong mixture could cancel out [the protection of the vaccine] or have adverse effects.” • A pediatric nurse came to Project Veritas to blow the whistle on New York contracted healthcare provider DocGo, and their subsidiary Ambulnz, who may have jeopardized the safety of thousands of people, including young children, through negligent administration of the COVID-19 vaccine. • Recordings from the whistleblower show fellow medical staff acknowledging mistakes of improperly mixing and administering the Pfizer children’s vaccine with the wrong diluent (bacteriostatic water), lack of proper training, lack of incident reporting. • Pfizer, the CDC, and the FDA are all very clear: the COVID-19 vaccine should only be administered with the proper saline solution; bacteriostatic water is NOT to be used. • Project Veritas reached out to Pfizer, multiple doctors, and scientists.

None were able to state with certainty what the adverse effects are on children getting the wrong mixture, or adults getting overdosed with the COVID-19 vaccine. [NEW YORK, NEW YORK– January 26, 2022] Whistleblower recordings obtained by Project Veritas appear show medical staff and supervisors admitting they used the wrong dilutant in giving the COVID-19 Vaccine to children, lower income, and homeless adults, and confirming the error “could cancel out [the protection of the vaccine] or have adverse effects.” The company, DocGo and their subsidiary Ambulnz, failed to disclose the incidents. It is also unclear if any affected patients were ever notified. The recordings, which come from a whistleblower employed through DocGo/Ambulnz, show nurses and other staff admitting they may have improperly mixed the COVID-19 Vaccine with bacteriostatic water instead of saline solution. Pfizer, the CDC, and the FDA give clear instructions about diluents saying bacteriostatic water is not to be used. Audio and video recordings, however, show nurses admitting that the erroneous mixture “could cancel out [the protection of the vaccine] or have adverse effects.”

It is unclear if patients, including parents of children who were vaccinated, were ever notified, despite company supervisors appearing to be aware of the problem. According to the nursing staff, no incident reports were filed. The potential risk to children who received the botched mixture was so significant that a nurse with DocGo/Ambulnz said she felt compelled to reach out to Project Veritas. “These are little kids, these are babies,” said the whistleblower during an emotional interview with Project Veritas founder James O’Keefe. Guy Banks, a supervisor with DocGo/Ambulnz can be heard attempting to instruct staff on how to properly vaccinate patients over the phone. “Make sure it’s the right one, because some people got the wrong one,” Banks is heard saying, in reference to the diluents paired with COVID-19 vaccines. The whistleblower’s recollection of the lack of training is astonishing. “On my first day there were no instructions about mixing the vaccine. I called the supervisor and asked, ‘how do I dilute this vaccine?’ He told me to ‘YouTube it.’ We were never given an in-service,” said the whistleblower. Proper in-service training is mandatory standard operating procedure in the medical field. Project Veritas reached out to DocGo for comment spoke with President Anthony Capone who touted the training of DocGo medical staff and denied the possibility that patients received the wrong vaccine mixture. “We have no circumstances in company history when bacteriostatic water was used in diluting vaccine,” Capone said. He added that the footage could be describing “wrong stuff pulled from the shelves” but ultimately replaced before vaccines were administered. A full version of Capone’s response to the Project Veritas release is available at projectveritas.com.
 

marsh

On TB every waking moment

EXCLUSIVE: Doctor Treating Covid Patients For Free: ‘Fauci Is The Greatest Mass Murderer In History,’ ‘Hellspitals Are The New Concentration Camps’

By Alicia Powe
Published January 26, 2022 at 5:15pm

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The measures taken by the federal government and administered nationwide to “stop the spread” and mitigate COVID-19 infection is actually a ploy implemented by “Nazi Fauci” to institute a one-world government and legalize mass murder, warns Dr. Ben Marble, a Florida-based Family Medicine Specialist.

“This is mass genocide. Nazi Fauci is the greatest mass murderer in the history of the world. He needs to be arrested and on trial for Nuremberg 2.0 along with Bill Gates and George ‘Sarass,’ Nazi Klaus Schwab – all the billionaire elite,” Dr. Marble told the Gateway Pundit at the Defeat the Mandate rally in Washington, DC.

“This is a takedown of America to bring in the one-world government plan. The mRNA gene therapy or the DNA therapies — those are not vaccines. They are experimental gene therapy,” he continued. “Definitely— nobody needs a vaccine for Covid. Even if it was a real vaccine that actually worked, we don’t need a vaccine for Covid.”

By April 2020, after working in the hospital treating Covid patients around the clock, Marble concluded everything being recommended by the Center For Disease Control and ‘Nazi Fauci’ to treat the newly spawning coronavirus “was just totally wrong” and “actually the opposite of everything we should do.”

Despite the potential backlash, Marble decided to ignore Fauci and the federal government and “start delivering early treatment to my patients.”

WATCH:
Rumble video 9:02 min

As the number of coronavirus fatalities continued to spike amid systemic adherence to new illogical CDC regulations, Marble began treating Covid patients for free:
“At that time, I had been doing some telemedicine and I had this strange thing. I had a short dream about Jesus, and he told me I should treat my patients for free. I thought, ‘How am I going to do that? I don’t own the hospital.’ And he looked at me and said, ‘Well, I healed the blind for free’ and then laughed at me. And then I woke up, that was the end of the dream,” the doctor explained. “I didn’t think much of it.
“Then, a week or so later, Trump came on television, and he said he wanted doctors to practice medicine across state lines. I instantly had this eureka moment in my head and thought, ‘Wow, I can treat patients in all 50 states, so maybe I’ll just treat them for free.’ And so, I did.”
At least 866, 968 Americans have died from Covid according to the United States as of Jan. 25, 2022, according to data published by the Center For Disease Control. Most did not die from the virus, but the hospitals’ murderous protocol, Marble contends:
“There are 1.1 million physicians in America and there are probably less than 1,000 that are willing to treat Covid patients early. I call them ‘Fauci doctors.’ The Fauci doctors across America, have abandoned their patients. We have an epidemic, a pandemic of malpractice, where people get sick from Covid. Their doctor abandons them, committing malpractice,” he said. “They won’t give them any treatment at all and tell them, ‘Don’t come to my office because they are afraid and don’t want to catch it. And if you’re dying, go to the hospital.
Even Covid lockdowns, forced quarantine measures, are part of the anti-American plan to depopulate.

“Obesity is one of the biggest risk factors, but everything that they want you to do, they want you to stay home be lazy and get fat, which makes your risk of dying even higher,” Marble continued. “So, literally everything the CDC and Fauci — literally, everything they do is to maximize death.”
 

marsh

On TB every waking moment

Whistleblowers Reveal DoD Medical Data Showing Military Cancer Diagnoses HAVE TRIPLED Since The Rollout Of The Experimental Vaccines – Along With a 10x Increase in Neurological Disorders and a Near 5x increase in Female INFERTILITY – (VIDEO)

By Julian Conradson
Published January 26, 2022 at 2:00pm

Military-vaccine-913x479.jpg

On Monday, several world-renowned doctors and medical experts spoke during a panel discussion in Washington DC that was hosted by Senator Ron Johnson (R-WI),

The nearly five-hour-long event, which was titled “Covid-19: A Second Opinion,” saw a wide range of issues discussed, including “the global pandemic response, the current state of knowledge of early and hospital treatment, vaccine efficacy, and safety, what went right, what went wrong, what should be done now, and what needs to be addressed long term,” according to its description on Sen. Johnson’s website.

The esteemed medical experts sounded the alarm over several issues that they have come across over the past year, exposing even more damning information that illustrates the horrific effects of the experimental vaccines, and how the corrupt US health regime has nefariously attempted to cover its tracks since the beginning.

Unfortunately, the catastrophic effects of the vaccines may be worse than ever thought possible, especially for young people.

During the event, Ohio attorney Thomas Renz presented DOD medical billing data from the Defense Medical Epidemiology Database (DMED) that exposes the disturbing truth about what is happening to the health of our service members since the rollout of the jab a year ago.

According to Renz, there has been an astronomical increase in several serious illnesses and disorder diagnoses in the US military since the rushed rollout of the Covid-19 vaccine – most concerning of which – cancer, which has seen a 3x increase.
“We have substantial data showing that we saw, for example, miscarriages increasing by 300% over the five-year average, almost. We saw almost 300% increase in cancer over the five-year average.”
The DMED data also revealed that there has been a whopping ten times increase in neurological disorders since the vaccines were introduced, which directly impacts military readiness, especially within the US Air Force.

Not the most encouraging thing, considering the Warhawks in the DC Swamp are pushing to kick off WWIII with Russia.
“We saw — this one’s amazing — neurological. So, neurological issues which would affect our pilots, over 1000% increase. 1000,” he said.
Completely flabbergasted by the revelation, Sen. Johnson asked Renz to clarify: “Ten times,” he said. “That’s ten times the rate?”

Renz continued:
“82,000 per year to 863,000 in one year. Our soldiers are being experimented on, injured, and sometimes possibly killed.”
WATCH:
View: https://twitter.com/i/status/1485695818996854788
2:20 min

Senior editor Daniel Horowitz of the Blaze spoke with Renz and corroborated the information with the whistleblowers to confirm the data’s legitimacy. According to Horowitz, who personally ‘knows two of the three whistleblowers,’ the number of cancer diagnoses in the military went from a 5-year average (2016-2020) of 38,700 per year to 114,645 in the first 10 months of 2021.

Horowitz explained:
“I know 2 of the 3 cited whistleblowers. Their credentials are impeccable. Lt. Col. Chambers is one of the only Green Beret doctors in the military.
Actually I got that wrong. One of the whitsleblowers just told me it was through October, not November. So this is 10 months of data off the chart vs. prior 12 month years!”

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Further adding to the credibility of it all, the military whistleblowers provided their testimony under oath, which will be used in federal court by Renz.

From The Blaze:
“In a declaration under penalty of perjury that Renz plans to use in federal court, Drs. Samuel Sigoloff, Peter Chambers, and Theresa Long — three military doctors — revealed that there has been a 300% increase in DMED codes registered for miscarriages in the military in 2021 over the five-year average.
The five-year average was 1,499 codes for miscarriages per year. During the first 10 months of 2021, it was 4,182.

As Renz explained to me in an interview with TheBlaze, these doctors queried the numbers for hundreds of codes from 2016 through 2020 to establish a baseline five-year average. These codes were generally for ailments and injuries that medical literature has established as being potential adverse effects of the vaccines.”
Renz also provided The Blaze with additional information on other severe illnesses and disorders that he did not have time to get to during the panel discussion.

The scope of the damage is absolutely shocking. In addition to the 3x of cancer and miscarriages, and the 10x of neurological disorders, there has been a near 5x spike in female infertility, among others.
“Some other numbers he did not mention at the hearing but gave to me in the interview are the following:
The data comes directly from the US military’s Defense Medical Epidemiology Database (DMED) system, which is the military’s equivalent to the US Vaccine Adverse Events Reporting System (VAERS) – but the DMED system is only accessible by military doctors and records every single case in the military for insurance billing, which, unlike VAERS, makes it extremely accurate.

As Horowitz also points out, this military-medical information is easily accessible to the federal government’s alphabet agencies (FDA, CDC, DoD) that are in charge of creating the public health nightmare we are living through, which indicates they are well aware of the skyrocketing diagnoses of life-threatening reactions that are linked to the experimental vaccine – but have decided to cover up the information from the public while they continue to compel more jabs.

In short, Biden’s federal government is fully aware of what’s going on, but the narrative and their corruption are more important than American lives, even if they are military members.

According to Renz, the whistleblowers came forward because of what they were seeing on the job as they treated military personnel, leading them to investigate the DMED system for anomalies related to the increase they had seen in their clinical experience.

Unfortunately, their investigation confirmed what they had feared, and things have just been getting worse.

This is just “the tip of the iceberg,” claimed Renz, who says he has even more data coming.

One of the whistleblowers explained to The Blaze:

“‘These doctors were motivated to explore DMED data due to the numbers of case increases they were seeing empirically,’ said the whistleblower, who served in the military for many years. ‘Some physicians throughout the force (all branches) have been intimidated by commands not to perform the full spectrum of testing and adhere to the regulations, which implicitly direct full workups for EUA vaccination adverse reactions. It will require other military physicians to step forward and share experiences to fully ascertain the enormity of these allegations and engender an investigation to the fullest extent.’

Renz claims he has a video with two witnesses showing the entire process of downloading this data from the database and is prepared to present it in court. He also told me that this is just ‘the tip of the iceberg,’ as the codes have increased exponentially in numerous other diagnosis categories. Renz said his spreadsheet, which includes over 100 medical diagnosis categories, was shared with Senator Johnson and his staff before the Monday hearing.”
During Monday’s hearing, Renz also testified that some of the data, specifically related to myocarditis, have been manipulated since the whistleblowers pulled the data out of the DMED system, indicating that the federal government is attempting to cover its tracks.

Following Renz’s bombshell revelations, Sen. Johnson warned Biden’s corrupt regime that they have officially been put “on notice,” and better not delete any of the data.
“The Department of Defense, the Biden administration is on notice they must preserve these records and this must be investigated.”
If the data is accurate, and there is no indication that it isn’t (especially considering the corroborating data in VAERS, countless medical studies showing the adverse effects of the vaccine, and the manipulation of Covid statistics that has already been exposed), Biden’s federal government has committed atrocious crimes against humanity and has been working overtime to criminally conceal them from the pubic.

We are way past due for some major accountability.
 

marsh

On TB every waking moment
(Denmark)


Denmark to Lift All Remaining Covid Restrictions by February

By Cristina Laila
Published January 26, 2022 at 1:03pm
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Denmark will lift all Covid restrictions by February 1 after UK, Ireland and the Netherlands made similar announcements.

Reuters reported:
Denmark aims to scrap all remaining domestic COVID-19 restrictions next week, following on from similar announcements in the UK, Ireland and the Netherlands in the past week despite high numbers of Omicron infections in Europe.

The Nordic country already loosened restrictions two weeks ago after a month-long lockdown, allowing cinemas and music venues to reopen, but some rules remain, including limited opening hours for restaurants and mandatory face masks. read more

In a letter to parliament, Health Minister Magnus Heunicke said the government intends to follow recommendations issued by an expert panel on Tuesday to scrap all restrictions by Feb 1.

The government’s decision, which is subject to parliamentary approval, will be the most far-reaching easing of curbs seen among the Nordic countries.
The Republic of Ireland scrapped nearly all Covid restrictions last Saturday.

UK Prime Minister Boris Johnson also announced Covid restrictions in England would be lifted.

Meanwhile in the United States, Joe Biden and the Democrats are pushing for more Covid tyranny.
 
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