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Re: The FDA Wants You to Forget It Told 'Y'all' to Stop Taking Horse Dewormer

By: Fiz in 6TH POPE | Recommend this post (0)
Tue, 22 Nov 22 4:22 PM | 24 view(s)
Boardmark this board | 6th Edition Pope Board 		Msg. 37664 of 58656
(This msg. is a reply to 37661 by Decomposed)
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IMO, the Founders biggest mistake in framing the Constitution and Bill of Rights was to not stipulate a minimum “make whole” PERSONAL penalty for anyone who was later found to have violated someone else's personal rights.

That has produced a 250-year joke of "VIOLATE SOMEONE ELSES' CONSTITUTIONAL RIGHTS EARLY AND OFTEN". IF (big if) anyone ever sues you for violating their Constitutional rights your penalty will be little or nothing of what you already gained by raping them to begin with.

It should have been MORE LIKE 100% PERSONAL LIABILITY WITH NO Statute of limitations. And, ideally, 100X penalties if you are judged to have been reckless or wonton in your trampling of the Constitution.

Put differently, the Bill of Rights was the first attempt to “fix” the lacks in the first draft of the Constitution, with the first TEN amendments. There needed to be a ZEROTH Amendment which made for VERY onerous, inescapable, PERSONAL penalties against anyone who violated someone else's Constitutional rights. If the violation was both egregious and deliberate, citizenship - and most protections under the law - should have been stripped from the offender. People, and especially GOVERNMENT people, would be a lot more careful in abuse of power.

What we have endured, because of this lack, is 250 years of MOSTLY DELIBERATE Constitutional abuse, as people in power realized there were no real consequences, especially for government workers, of recklessly—or even deliberately—violating the, supposed, "Law of the Land"...

It is hard to believe the Founders missed this obvious deficiency by “mistake”. Perhaps they figured getting the first ten amendments through was as much as they could dare hope for. Because of this, I am calling the US Constitution as now COOKED and not fixable. I honestly think it is time to move on, and out, from the US, although how to do that is neither easy nor obvious.

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The above is a reply to the following message:
The FDA Wants You to Forget It Told 'Y'all' to Stop Taking Horse Dewormer
By: Decomposed in 6TH POPE
Tue, 22 Nov 22 10:04 AM 		Msg. 37661 of 58656

I downed a fifth of a tube of ivermectin-for-horses each day commencing with my wife's cold symptoms. Ten days later, I too tested positive for Covid. Two weeks after that, I tested negative and stopped taking the ivermectin. My experience with this horrible disease can be summed up as a "piece of cake." I had a runny nose for two weeks. That was the worst of it. Maybe the ivermectin played a role and maybe it didn't. All I know is I used it and got the desired outcome.

Another interesting tidbit: One of my two co-morbidities is that I'm on blood-thinner for the rest of my life. (The other co-morbidity is the mechanical heart valve.) But the thin blood they call a risk may actually lower my risk of ever getting one of those ugly spike-protein clots. Sometimes it's better to be lucky than good. - De

November 21, 2022

The FDA Wants You to Forget It Told 'Y'all' to Stop Taking Horse Dewormer

by Stacey Lennox
PJmedia.com


In June, three doctors filed a lawsuit against the Food and Drug Administration (FDA) for interfering with using ivermectin to treat COVID-19. All three were disciplined for prescribing human-grade ivermectin to treat patients. The attorney for the physicians, Boyden Gray, asserted the FDA’s actions regarding ivermectin went against well-established law and practice regarding the off-label use of FDA-approved drugs.

When the suit was filed, Gray told the Epoch Times, “Congress recognized the importance of letting doctors be doctors and expressly prohibited the FDA from interfering with the practice of medicine.” He continued, “That is exactly what the FDA has done repeatedly throughout this pandemic, assuming authority it doesn’t have and trying to insert itself in the medical decisions of Americans everywhere.”

In a hearing on November 1, the FDA’s lawyers argued, “The cited statements were not directives. They were not mandatory. They were recommendations. They said what parties should do. They said, for example, why you should not take ivermectin to treat COVID-19. They did not say you may not do it, you must not do it. They did not say it’s prohibited or it’s unlawful. They also did not say that doctors may not prescribe ivermectin.”

That’s some pretty innovative hair-splitting. It is almost as if the FDA doesn’t know that in a medical system full of attorneys, statements like this would not chill the use of a drug:

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The attached article even says, “The FDA has not authorized or approved ivermectin for use in preventing or treating COVID-19 in humans or animals. Ivermectin is approved for human use to treat infections caused by some parasitic worms and head lice and skin conditions like rosacea.” The sentence implies to those who do not know better that the FDA must approve a medication for a specific use.

The language the agency used matters, though. A 20% bonus was provided if hospitals used “drugs of biologicals approved by the Food and Drug Administration (FDA) for COVID-19 .” Coupled with the bribe for hospital administrators, the FDA not “approving” ivermectin and other repurposed drugs for use effectively prohibited them.

However, if the FDA wants to play this game, someone should ask if it has “approved” the use of gonadotropin-releasing hormone (GnRH) agonists in young adults in cases of gender dysphoria. To be clear, the agency has not. Some of the reported side effects that bear investigation with these drugs are infertility, lifelong sexual dysfunction, and cardiac issues. Yet a search of the FDA’s Twitter profile does not contain a tweet saying, “You aren’t a dude, and no medication is going to change that.”

Nor does the agency seem bothered by the fact that Pfizermectin, also called Paxlovid, interacts with dozens of commonly used prescription and non-prescription medications. Precautions must be taken with medicines as divergent as hormonal contraceptives, cardiac medications, and cancer drugs when Paxlovid is prescribed. The FDA also does not seem bothered that patients who take it seem to suffer from “rebound” cases of Covid. Yet, this medication is approved by the FDA to be used in the outpatient treatment of COVID-19. So is remdesivir, which was never demonstrated to improve mortality rates. It only showed the ability to shorten hospital stays.

Perhaps most infuriating, the FDA does not seem bothered by the idea that people may have died in cases where the drug was withheld. Some doctors treated people infected with COVID-19 on an outpatient basis using combinations of medications that included ivermectin. These physicians, like Dr. Harvey Risch and Dr. Pierre Kory, estimate that 50% or more of the patients who died of Covid could have recovered if the outpatient protocols were used after they were developed. That equates to hundreds of thousands of people in the United States.

Other doctors were using these medications with inpatients. One is renowned critical care physician Dr. Paul Marik. According to his biography, Dr. Marik has written over 500 peer-reviewed journal articles and 80 book chapters and authored four critical care books. He is the world’s second most published critical care physician and has been cited over 43,000 times in peer-reviewed publications.

When Covid hit, Dr. Marik did what we all thought doctors were supposed to do. He sought to relieve his patients’ suffering and death by treating their symptoms with repurposed medications indicated by research and his practical experience. He found success treating patients in the ICU with the MATH+ protocol. The protocol included ivermectin along with steroids for inflammation and other existing medications. According to Dr. Marik, his mortality rate was half that of his colleagues.

Then a memo came from the hospital administration. It prohibited the use of the medications on the protocol Marik was using, including vitamin C. The only drug available for use was remdesivir because it was “approved” by the FDA, so it also carried a financial incentive. You can listen to Dr. Marik’s voice crack as he recounts being forced to helplessly watch his seven patients die and the subsequent removal of his hospital privileges.

Dr. Marik is one of the plaintiffs in the lawsuit against the FDA. His career and the lives of his patients are a direct cost of the FDA’s so-called “recommendations.” The agency cannot be allowed to whitewash its role in preventing doctors from practicing medicine through political and financial pressure or be held harmless for the lives its actions caused.

http://pjmedia.com/columns/stacey-lennox/2022/11/21/the-fda-wants-you-to-forget-it-told-yall-to-stop-taking-horse-dewormer-n1647626

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