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U.S. Public Health Agencies Aren't ‘Following the Science,’ Officials Say

Shiloh

Editor, Senior Moderator
Source: https://www.commonsense.news/p/us-p...?r=abaxo&s=r&utm_campaign=post&utm_medium=web

U.S. Public Health Agencies Aren't ‘Following the Science,’ Officials Say
‘People are getting bad advice and we can’t say anything.’
Marty Makary M.D., M.P.H.
and Tracy Beth Høeg M.D., Ph.D.
Jul 14

The calls and text messages are relentless. On the other end are doctors and scientists at the top levels of the NIH, FDA and CDC. 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 their 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.’”...
 
WHO is captured, too.


https://www.youtube.com/watch?v=PLo2Wwa3NNA

Omicron Boosters, Kids' Vaccine & More (w/Dr. Paul Offit)
61,829 views Jul 6, 2022 Why did Dr. Offit vote NO on Omicron-specific boosters at the FDA advisory meeting? What's up with vaccine for the youngest kids? AND MUCH MORE...

Transcript:

"So you don’t really have animal model studies that support this. You don’t have, as far as I’m concerned, neutralizing antibody study data that supports this. And I guess the thing that is most upsetting to me is normally when you get something from the FDA, when we have these meetings, so you usually get it a few days before you meet, you usually get a couple hundred pages. And actually before the June 14th meeting about pediatric vaccines, we got 440 pages to read about three days before the meeting. They assume that you don’t have a life, which is true, but I don’t think that they should assume that. So in any case here on the other hand, normally you get the EUA submission from the company, which is 85 to 100 pages long, and then you get the FDA’s review of all those data. It really, really is heartening. I mean, it is a very thorough review. Not here, here it was 22 pages from the FDA, which included 1/2 a page on Pfizer’s data and 1/2 a page on Moderna’s data. You could get that from the press release. In fact, it was no more detailed frankly than the press release. So I just thought the question we’re being asked is in the end always, is do the benefits outweigh the risks, even though the risks are generally small and sometimes unknown, that’s always the question. Do the benefits of this vaccine outweigh the risk? I didn’t see the benefits. I was surprised actually, frankly, that of the 21 voting members, 19 voted yes, ’cause I just didn’t see the evidence for that. And we’ll see how this plays out. I mean, this was something that I think they, that was desired by this administration. I could be wrong, but the way that this, the other thing that was odd about this meeting was that we’re an advisory committee. We’re being asked for our advice. So normally what happens is they just present the data. Here’s the data, what’s your advice? And people can ignore our advice. I mean I’m in academic medicine, people ignore my advice all the time, but to make the best advice. So here on the other hand, however, they had somebody from the WHO, Kanta Subbarao, who presented their opinion about this. And their opinion was they thought this was a good idea. And then you had the FDA presenting where they also had an opinion. That’s unusual. And then the next day, you know, you read a public health announcement from the, a press release from HHS Health and Human Services that says that the government has decided to purchase at least 105 million doses from Pfizer with up to 300 million doses. It was a little unclear from that press release, but they mentioned that we had just made this decision the day before. So you just sort of felt like the fix was in a little bit here. Maybe that’s not the right phrase, but it was something that they wanted. And I felt like we were being led here with a critical lack of information. So we’ll see how this turns out. But I didn’t like this."
 
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