Vaccine Mandates: An Inversion of Medical Ethics and a Reversal of Public Health Policy

Vaccine Mandates: An Inversion of Medical Ethics and a Reversal of Public Health Policy

The arguments of Jane M. Orient written over two decades ago on the nature of mandatory vaccines still ring true today:

Mandates have a profound effect on medical practice. Once a vaccine is mandated for children, the manufacturer and the physician administering the vaccine are substantially relieved of liability for adverse effects. (3) The relationship of patient and physician is shattered: in administering the vaccine, the physician is serving as the agent of the state. To the extent that the physician simply complies, without making an independent evaluation of the appropriateness of the vaccine for each patient, he is abdicating his responsibility under the Oath of Hippocrates to “prescribe regimen for the good of my patients according to my ability and my judgment and never do harm to anyone.” Instead, he is applying the new population-based ethic in which the interests of the individual patient may be sacrificed to the “needs of society.”

If a physician advises against a mandated vaccine, he faces increased legal liability if the patient is infected with the disease. In addition, he may risk his very livelihood if he is dependent upon income from “health plans” that use vaccine compliance as a measure of “quality.”

It is perhaps not surprising, although still reprehensible, that physicians sometimes behave in a very callous manner toward parents who question the need for certain vaccines. I have even heard reports of physicians threatening to call Child Protective Services to remove the child from parental custody if a parent refused a vaccine — even after the child had screamed inconsolably for hours after each of the first two doses. The federal policy of mandating vaccines marks a monumental change in the concept of public health. Traditionally, public health authorities restricted the liberties of individuals only in case of a clear and present danger to public health. For example, individuals infected with a transmissible disease were quarantined. Today, a child may be deprived of his liberty to associate with others, or even of his supposed right to a public education, simply because of being unimmunized. Yet, if a child is uninfected, his unprotected status is not a threat to anyone else. On the other hand, immunization of a child who is already infected (or who becomes infected in spite of the vaccine) is of no protective value to anyone. This represents a reversal of the earlier policy of preventing exposure to infectious agents. In fact, it takes exposure — as to contaminated needles or promiscuous sex — as a given, while begging the question of whether protection against hepatitis B has any overall effect on morbidity or mortality in a population that also exposes itself to worse hazards.

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An Open Letter to Elizabeth Warren on Natural Gas Prices

An Open Letter to Elizabeth Warren on Natural Gas Prices

Senator Warren blamed natural gas CEOs for rising prices. Here’s how I would respond if I were them.

Dear Senator Warren,

Today, 12/7, is the deadline you gave natural gas CEOs to respond to your letter blaming them for rising natural gas prices—which you are in fact to blame for. Here’s how proud gas CEOs would answer you if they were not afraid of your political wrath.

Sincerely,

Alex Epstein
Energy expert
Founder and President, Center for Industrial Progress Author of The Moral Case for Fossil Fuels and Fossil Future
Creator of EnergyTalkingPoints.com

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Dear Senator Warren,

In your letter you claim “concern about rising natural gas prices,” which you attribute to my and other “energy companies’ corporate greed.”

But if you want to avoid unnecessarily high gas prices, you must recognize that they are your fault, not ours.

There are three basic facts that explain unnecessarily high natural gas prices:

  1. Prices are determined by supply and demand, not “greed.”
  2. America has an effectively unlimited supply of gas.
  3. You and other anti-gas politicians have artificially restricted the supply of gas.

 

Fact 1: Prices are determined by supply and demand, not “greed.”

If we could control natural gas prices in our favor, why didn’t we do so during unprofitable 2015-20? Our profits are determined by a) the market price for our product and b) our efficiency.1

When prices go up, it is crucial that companies can profit for two reasons.

  1. We earned our profit through efficiency.
  2. Profits motivate and make possible investment, which lowers long-term prices.

Your railing against our profits is unjust and shortsighted.

Fact 2: America has an effectively unlimited supply of gas

Thanks to the shale revolution, aka “fracking,” which you have tried to ban, the US has enough natural gas to supply us and other nations for decades just with current technology—and for centuries with future technology.2

The only thing that can stop our industry from producing low-cost natural gas for America and the world—including the billions of poor people whose lives we improve—is politicians who coercively restrict our otherwise limitless ability to produce low-cost natural gas.

Fact 3: You and other anti-gas politicians have artificially restricted the supply of gas

When you and other anti-gas politicians place draconian restrictions on natural gas production and transport, and threaten to do far worse, supply goes down and prices go up.

The number one bottleneck to lower gas prices is a lack of pipelines and export facilities to transport natural gas from where it is drilled to markets throughout the US and around the world. You have contributed to this problem by avidly opposing pipelines and export facilities.3

Another major cause of unnecessarily high gas prices is a lack of investment in natural gas, caused by political threats to the future of natural gas. No one has threatened the future of natural gas more than you. You have even talked about imprisoning executives of our industry!4

The worst imaginable thing that could happen for natural gas prices is to ban fracking–which is a crucial technology for almost 80% of American natural gas. Yet you have advocated a policy of “ban fracking—everywhere.” Do you now see what a catastrophe this would be?5

Senator Warren, I am deeply disappointed that rather than doing the right thing and addressing your role in unnecessarily high natural gas prices, you are instead denying it and advocating a policy that will make things far worse: further restricting natural gas transport.

I must also add that your call to prevent the export of natural gas during a global energy crisis is particularly harmful. The American natural gas industry is, for millions of poor people around the world, their greatest hope to be able to heat their homes this winter.

Senator Warren, you owe the American public and our industry an apology for 1) your numerous actions to drive up the price of natural gas, 2) your denial of responsibility, and 3) your unjust attack on an industry that sustains billions of lives.

Sincerely,

A Proud Gas Producer

You can read the letter in PDF form here and in talking point form here.

Here’s the Twitter version of my letter. If you use Twitter, please share it with Senator Warren (@SenWarren). If enough people bring attention to this letter there’s a good chance Senator Warren will feel compelled to respond.

References

1 U.S. Energy Information Administration – Natural Gas Prices https://www.eia.gov/dnav/ng/ng_pri_sum_dcu_nus_m.htm

2 “On my first day as president, I will sign an executive order that puts a total moratorium on all new fossil fuel leases for drilling offshore and on public lands. And I will ban fracking—everywhere.” https://twitter.com/ewarren/status/1170070887887986690
“Most of the production increases since 2005 are the result of horizontal drilling and hydraulic fracturing techniques, notably in shale, sandstone, carbonate, and other tight geologic formations.”
https://www.eia.gov/energyexplained/natural-gas/where-our-natural-gas-comes-from.php
“The U.S. Energy Information Administration (EIA) estimates that in 2020, U.S. dry shale gas production was about 26.3 trillion cubic feet (Tcf), and equal to about 79% of total U.S. dry natural gas production in 2020.” https://www.eia.gov/tools/faqs/faq.php?id=907&t=8
https://www.energy.gov/fecm/science-innovation/oil-gas-research/methane-hydrate

3 https://detroitnews.com/story/news/politics/2020/02/26/elizabeth-warren-calls-line-5-shutdown/4885611002/
https://www.enbridge.com/~/media/Enb/Documents/Factsheets/FS_Without_Line5_econ_impact.pdf
https://www.markey.senate.gov/news/press-releases/senators-markey-and-warren-to-reintroduce-legislation-to-block-infrastructure-used-to-export-americas-natural-gas

4 https://grist.org/article/elizabeth-warrens-new-plan-would-jail-lying-fossil-fuel-executives/
https://medium.com/@teamwarren/fighting-corporate-perjury-2346950a08b8

5 “On my first day as president, I will sign an executive order that puts a total moratorium on all new fossil fuel leases for drilling offshore and on public lands. And I will ban fracking —everywhere.” https://twitter.com/ewarren/status/1170070887887986690
“The U.S. Energy Information Administration (EIA) estimates that in 2020, U.S. dry shale gas production was about 26.3 trillion cubic feet (Tcf), and equal to about 79% of total U.S. dry natural gas production in 2020.” https://www.eia.gov/tools/faqs/faq.php?id=907&t=8

Steve Koonin: Is There a Climate Emergency?

Steve Koonin: Is There a Climate Emergency?

“The climate is the most complex system on Earth. Is it really possible to project with any precision what it will be like 20, 40, or even 100 years from now? Steve Koonin, former Undersecretary for Science in the Obama Administration, challenges the confident assumptions of climate alarmists.

The FDA & CDC: Why The U.S. Fails in COVID Testing

The FDA & CDC: Why The U.S. Fails in COVID Testing

From “Here’s Why Rapid COVID Tests Are So Expensive and Hard to Find“, ProPublica:

….Companies trying to get the Food and Drug Administration’s approval for rapid COVID-19 tests describe an arbitrary, opaque process that meanders on, sometimes long after their products have been approved in other countries that prioritize accessibility and affordability over perfect accuracy.

On the FDA treating private bio-tech companies like criminals:

After the FDA put out a call for more rapid tests in the summer of 2020, Los Angeles-based biotech company WHPM, Inc. began working on one. They did a peer-reviewed trial following the agency’s directions, then submitted the results this past March. In late May, WHPM head of international sales Chris Patterson said, the company got a confusing email from its FDA reviewer asking for information that had in fact already been provided. WHPM responded within two days. Months passed. In September, after a bit more back and forth, the FDA wrote to say it had identified other deficiencies, and wouldn’t review the rest of the application. Even if WHPM fixed the issues, the application would be “deprioritized,” or moved to the back of the line. “We spent our own million dollars developing this thing, at their encouragement, and then they just treat you like a criminal,” said Patterson. Meanwhile, the WHPM rapid test has been approved in Mexico and the European Union, where the company has received large orders.

An FDA scientist who vetted COVID-19 test applications told ProPublica he became so frustrated by delays that he quit the agency earlier this year. “They’re neither denying the bad ones or approving the good ones,” he said, asking to remain anonymous because his current work requires dealing with the agency.

On FDA micro-managing how the tests can be used making them expensive, and banning the private sale of cheap tests to the public:

FDA officials were particularly concerned about allowing tests to be administered outside the purview of a trained health care provider. “To mitigate the impact of false results, all Covid-19 tests authorized to date have been made available only by prescription, so that clinicians can interpret results for patients,” wrote Shuren and his deputy Dr. Tim Stenzel in an October 2020 column in The New England Journal of Medicine.

That cautious approach persisted all through the winter and early spring, despite rising agitation from the White House and Congress around the availability of tests.

“I actually have been saying that for months and months and months, we should be literally flooding the system with easily accessible, cheap, not needing a prescription, point of care, highly sensitive and highly specific” tests, White House chief medical advisor Dr. Anthony Fauci said under questioning from Schrier in a hearing on March 17.

On the FDA standing in the way of innovation and experimentation:

The FDA has been particularly circumspect with more novel approaches to testing, such as an olfactory test that detects the common COVID-19 symptom of loss of smell. The agency’s reviewers deprioritized an application for the scratch-and-sniff card even though it had been proven to stem transmission, said inventor Derek Toomre, a professor at the Yale School of Medicine.

On how the FDA bans tests approved in Europe:

For example, the biopharmaceutical giant Roche told ProPublica that it submitted a home test in early 2021, but it was rejected by the FDA because the trials had been done partly in Europe. The test had compared favorably with Abbott’s rapid test, and received European Union approval in June. The company plans to resubmit an application by the end of the year.

[…]

A smaller company, which didn’t want to be named because it has other contracts with the U.S. government, withdrew its pre-application for a rapid antigen test with integrated smartphone-based reporting because it heard its trial data from India — collected as the delta variant was surging there — wouldn’t be accepted. Doing the trials in the U.S. would have cost millions.

On how the central planning approach of “putting your eggs in one basket” fails:

In May, the CDC leaned hard into the message that vaccines were almost completely protective, mitigating the need for frequent testing. Manufacturers took that as a bad sign for testing volume. Abbott ramped down manufacturing of its popular home test.

[…]

“It has taken more than a year for the American public, scientific experts and academia to accept the important role of rapid testing in the U.S.,” Koval said. “Overseas, that was not the case, because the value of rapid testing was better understood prior to the pandemic.”

Read the rest.

Recommended Reading:

Peikoff & Chayes: What To Do About Facebook

Peikoff & Chayes: What To Do About Facebook

If you thought Facebook was manipulative and bad, having the state control its manipulative instruments would be Orwellian, so conclude Peikoff and Chayes:

“For years, congressional hearings pertaining to all (un)imaginable evils of social media have amplified a persistent argument that they must be regulated, controlled – even declared public utilities. Now the groundwork is laid to fully implement Orwell’s “1984 by the stroke of a pen.”

[…]

“But most importantly – and this is where we part ways with Haugen – we must prevent the government from obtaining any further control over instruments that apparently cannot be responsibly handled, even by a bunch of gifted Whiz Kids in the Valley.”

“We should staunchly oppose any legislation that puts not only personal data, but also manipulative algorithms at the disposal of politicians or bureaucrats, as some of the laws proposed during Tuesday’s hearing might entail. Private lawsuits, made more practicable by a narrower interpretation of Section 230, would help redress grievances of users of all ages.  

“Big Brother, which is precisely what a public-private “partnership” with Facebook might look like, isn’t any less pernicious if it’s spawned “for the children.”

Read “Facebook hearings confirm fears about company’s business model. What now?

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