Sunday, July 17, 2022


A belated victory against COVIDiocy

In a belated victory against COVID insanity, a state Supreme Court judge has declared null and void New York’s Rule 2.13, endowing the state health commissioner with unbounded power to issue isolation and quarantine orders.

Enacted in February 2022 and renewed since, the regulations have been published in the state register for possible permanent adoption. Yet it would be madness to codify this power months after the real threat of COVID receded into nothing.

Lunatic, too, given New York’s atrocious record on protecting the most vulnerable (i.e. the elderly) from the virus.

Kudos to state Sen. George Borrello (R.-Chautauqua) and his fellow complainants on their successful lawsuit over the rule — and to Judge Ronald Ploetz for his ruling.

The rule, which Ploetz noted paid only “lip service” to the Constitution, was itself the fruit of a poison tree: the overbroad powers the Legislature granted then-Gov. Andrew Cuomo at the pandemic’s start.

Cuomo used those powers not only to shutter the state’s economy, but to serve special interests like the hospital lobby, including via the deadly mandate for care homes to admit COVID-positive patients. The state is still reeling from his dictatorial pseudoscience today.

But COVID rules were never about science. On the numbers, Cuomo’s draconian policies had no significant effect on our outcomes when compared to states with far more liberal rules. And Cuomo himself seemed to break them whenever the mood was on him.

Those rules were about power, exercised by fanatics and hypocrites. By blocking one of them, Judge Ploetz has done New York a great service.

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US agencies aren’t ‘following the science’ on COVID — and staff are too scared to complain

By Marty Makary and Tracy Beth Høeg

The calls and text messages are relentless. On the other end are doctors and scientists at the top levels of the National Institutes for Health, Food and Drug Administration and Centers for Disease Control and Prevention. They are variously frustrated, exasperated and alarmed about the direction of the agencies to which they have devoted their careers.

“It’s like a horror movie I’m being forced to watch and I can’t close my eyes,” one senior FDA official lamented. “People are getting bad advice and we can’t say anything.”

That particular FDA doctor was referring to two recent developments inside the agency. First, how, with no solid clinical data, the agency authorized COVID vaccines for infants and toddlers, including those who already had COVID. And second, the fact that just months before the FDA bypassed its external experts to authorize booster shots for young children.

That doctor is hardly alone.

At the NIH, doctors and scientists complain to us about low morale and lower staffing: The NIH’s Vaccine Research Center has had many of its senior scientists leave over the last year, including the director, deputy director and chief medical officer. “They have no leadership right now. Suddenly there’s an enormous number of jobs opening up at the highest level positions,” one NIH scientist told us. (The people who spoke to us would only agree to be quoted anonymously, citing fear of professional repercussions.)

The CDC has experienced a similar exodus. “There’s been a large amount of turnover. Morale is low,” one high level official at the CDC told us. “Things have become so political, so what are we there for?” Another CDC scientist told us: “I used to be proud to tell people I work at the CDC. Now I’m embarrassed.”

Why are they embarrassed? In short, bad science.

The longer answer: that the heads of their agencies are using weak or flawed data to make critically important public health decisions. That such decisions are being driven by what’s politically palatable to people in Washington or to the Biden administration. And that they have a myopic focus on one virus instead of overall health.

Nowhere has this problem been clearer — or the stakes higher — than on official public-health policy regarding children and COVID.

First, they demanded that young children be masked in schools. On this score, the agencies were wrong. Compelling studies later found schools that masked children had no different rates of transmission. And for social and linguistic development, children need to see the faces of others.

Next came school closures. The agencies were wrong — and catastrophically so. Poor and minority children suffered learning loss with an 11-point drop in math scores alone and a 20% drop in math pass rates. There are dozens of statistics of this kind.

Then they ignored natural immunity. Wrong again. The vast majority of children have already had COVID, but this has made no difference in the blanket mandates for childhood vaccines. And now, by mandating vaccines and boosters for young healthy people, with no strong supporting data, these agencies are only further eroding public trust.

One CDC scientist told us about her shame and frustration about what happened to American children during the pandemic: “CDC failed to balance the risks of COVID with other risks that come from closing schools,” she said. “Learning loss, mental health exacerbations were obvious early on and those worsened as the guidance insisted on keeping schools virtual. CDC guidance worsened racial equity for generations to come. It failed this generation of children.”

An official at the FDA put it this way: “I can’t tell you how many people at the FDA have told me, ‘I don’t like any of this, but I just need to make it to my retirement.’ ”

Right now, internal critics of these agencies are focused on one issue above all: Why did the FDA and the CDC issue strong blanket recommendations for COVID vaccines in children?

Three weeks ago, the CDC vigorously recommended mRNA COVID vaccines for 20 million children under five years of age. Dr. Rochelle Walensky, director of the CDC, declared that the mRNA COVID vaccines should be given to everyone six months or older because they are safe and effective.

The trouble is that this sweeping recommendation was based on extremely weak, inconclusive data provided by Pfizer and Moderna.

Few young kids get COVID-19 vaccination in the Big Apple
Start with Pfizer. Using a three-dose vaccine in 992 children between the ages of six months and 5 years, Pfizer found no statistically significant evidence of vaccine efficacy. In the subgroup of children aged six months to two years, the trial found that the vaccine could result in a 99% lower chance of infection — but that they also could have a 370% increased chance of being infected.

In other words, Pfizer reported a range of vaccine efficacy so wide that no conclusion could be inferred. No reputable medical journal would accept such sloppy and incomplete results with such a small sample size. More to the point, these results should have given pause to those who are in charge of public health.

Referring to Pfizer’s vaccine efficacy in healthy young children, one high-level CDC official — whose expertise is in the evaluation of clinical data — joked: “You can inject them with it or squirt it in their face, and you’ll get the same benefit.”

Moderna’s results — it conducted a study on 6,388 children with two doses — were not much better. Against asymptomatic infections, it claimed a very weak vaccine efficacy of just 4% in children aged six months to two years. It also claimed an efficacy of 23% in children between two and six years old, but neither result was statistically significant. Against symptomatic infections, Moderna’s vaccine did show efficacy that was statistically significant, but the efficacy was low: 50% in children aged six months to two years, and 42% in children between two and six years old.

Then there’s the matter of how long a vaccine gives protection. We know from data in adults that it’s generally a matter of months. But we have no such data for young children.

“It seems criminal that we put out the recommendation to give mRNA COVID vaccines to babies without good data. We really don’t know what the risks are yet. So why push it so hard?” a CDC physician added. A high-level FDA official felt the same way: “The public has no idea how bad this data really is. It would not pass muster for any other authorization.”

And yet, the FDA and the CDC pushed it through. That slap in the face of science may explain why only 2% of parents of children under age five have chosen to get the COVID vaccine, and 40% of parents in rural areas say their pediatricians did not recommend the COVID vaccine for their child.

More here:

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Also see my other blogs. Main ones below:

http://edwatch.blogspot.com (EDUCATION WATCH)

http://antigreen.blogspot.com (GREENIE WATCH)

http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)

http://australian-politics.blogspot.com/ (AUSTRALIAN POLITICS)

http://snorphty.blogspot.com/ (TONGUE-TIED)

https://immigwatch.blogspot.com/ (IMMIGRATION WATCH)

https://awesternheart.blogspot.com/ (THE PSYCHOLOGIST)

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