Archive for the ‘Treatment’ Category

COVID Clots or ‘Vaccine’ Clots? That is the Question

http://  Approx. 7 Min

COVID Clots

Full Measure With Sharyl Attkisson

Apr 8, 2024

For whatever reason, America’s health officials haven’t seemed publicly interested in answering a crucial question: How many illnesses and deaths can be attributed to COVID versus the vaccines or some combination?

Today, we look at shocking and graphic evidence that independent researchers are trying to make sense of, in the absence of helpful guidance from the usual authorities: a mysterious fibrous material being discovered in the veins and arteries of the dead.

A caution: some of the images in our report are graphic. 

______________

**Comment**

This information has been reported on for literally years, yet crickets from mainstream media, medicine, government and public health.

They simply don’t care.

Embalmer Steve Hirschman has been reporting on these mysterious, fibrous white clots for some time.  He’s finding them in every age group. He also states they are not made of blood like standard “blood” clots.  He has been accused of being unethical by sharing what he’s seeing.

Every single other embalmer he has had contact with is finding the same thing.

Since no governmental agency is following up on this, Former Airforce Major Tom Havalind has started to document and quantify these cases. Through a survey, he has asked over 200 embalmers what they are seeing, if they are seeing these clots, when they started seeing them, where on the body, and what percentage have them.

  • 73% of embalmers responded that they are seeing this type of clot
  • about 1 in 5 corpses have these clots in 2023
  • none reported seeing these clots prior to the ‘pandemic’ or the beginning of mass ‘vaccination’ with the COVID gene therapy
Havalind submitted his results to the FDA but he’s heard nothing back.

The FDA; however, did respond back to Full Measure with the following trite statement:

The FDA and the CDC place a high priority on vaccine safety and are committed to our vaccine safety monitoring program. The FDA has not identified any safety signals for fibrous blood clots with COVID-19 vaccines.

True to form the FDA wiggled out of responsibility by stating that since the observations were made on cadavers, it falls outside their purview.  

The top video is an excerpt from the following full program:

http://  Approx. 23 Min

COVID Concerns

Apr 8, 2024

In recent days, Colorado Representative Lauren Boebert announced she had emergency surgery for a blood clot and was diagnosed with an iliac vein problem called May-Thurner syndrome. Though it’s impossible to know the root cause, we’ve been reporting on a notable uptick in this very disorder, as reported by independent physicians treating thousands of patients. It’s one of many illnesses they say could be caused by, or worsened by, COVID or COVID vaccines.

One estimate from a NIH study implies up to one in four adults may be afflicted with long-term problems.

Today, the latest on what cutting-edge doctors are learning. 

Full Measure is a weekly Sunday news program focusing on investigative, original and accountability reporting. The host is Sharyl Attkisson, five-time Emmy Award winner and recipient of the Edward R. Murrow award for investigative reporting. She is backed by a team of award winning journalists. 

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Category:

Activism, Treatment, vaccines, Viruses

Congress’ Lip Service Against ‘Pandemic’ Treaty & WHO Focused on Profitable Disease X

http://

4/2/23

Senate Resolution 81 and ‘No WHO Pandemic Preparedness Treaty Without Senate Approval Act’ Rots in Committee

Congress is simply doing lip-service in protecting the public from global tyrants while the Biden Administration is all in to have our rights taken away.

Without intervention, we hand over our rights to the WHO to do the following:

  • Define the next pandemic
  • Determine lockdowns
  • Surveillance power
  • Determine treatments
  • Vaccine Mandates
  • Vaccine distribution
  • Vaccine IP and profits
  • Redistribution of …..everything – all resources.

The Louisiana Senate has passed legislation (SB 133) to make the state independent from directives and mandates that originate from international institutions including the WHO, UN, and WEF.  It states that the WHO, UN, and WEF shall have no jurisdiction or power within the state of Louisiana.  No rule, regulation, fee, tax, policy, or mandate of any kind of the WHO, UN, and the WEF shall be enforced or implemented by the state of Louisiana or any agency, department, board, commission, political subdivision, governmental entity of the state, parish, municipality, or any other political entity.  It now needs to be passed by the House of Representatives and signed into law by the governor.

The anti-commandeering doctrine, under the U.S. Constitution’s Tenth Amendment, holds that the federal government cannot commandeer state and local resources for its own purposes, it follows that international bodies would not be able to either.

“We have watched a horror story unfold in front of us as time has shown that the ‘recommendations’ and coercive regulations from outside organizations such as the WHO have harmed hundreds of thousands of Americans who took a vaccine that they were told was safe and effective. Now, we are witnessing severe, long-term side effects and countless deaths because the ‘experts’ were wrong.” ~ Louisiana State Senator Valarie Hodges

The video also reviews history of how internal documents show the corrupt WHO paid sexual abuse victims in the Congo $250 each to cover up their crimes.

https://brownstone.org/articles/pandemics-a-business-opportunity/

Pandemics: A Business Opportunity

BY    APRIL 2, 2024 
 

Relax for a few minutes, sit back, and pretend morals and business ethics are redundant. Then imagine an infallible, risk-free business scheme in which you get to create the market, decide the product, manage its regulation, then have the power to confine people to their homes or remove their income until they submit to buying it. And no one can sue you or take you to court if it all goes wrong.

No legitimate government would allow that within its borders (except perhaps a few family-run or completely totalitarian ones), so aim higher and make this international, as it then ceases to be fantasy. All this is being negotiated within the WHO pandemic documents to be agreed by your government in two months’ time.

So, imagine:

  • Your organization will be a public-private partnership, so using taxpayer money but guided by the private sector.
  • You spin a story that a series of plagues are about to engulf humanity, exponentially increasing in frequency and severity (your partners own the media, so don’t be troubled by reality).
  • Then use public money to set up a surveillance network guaranteed to find virus variants (i.e. go and find nature, you can’t miss it).
  • Governments have agreed ahead of time to give you power to control healthcare policy when you decide these variants pose a threat (not harm, just a threat). They have agreed that this includes border closures, restrictions on daily life of their citizens, and of course mandated vaccination (in return for them ‘getting freedom back’).
  • Then transfer these virus variants to laboratories and pharmaceutical companies of your choice (your friends and supporters, who will in return give your organization some money).
  • The pharmaceutical companies are ready: They have been receiving free billions from taxpayers annually under the same scheme, to keep their production lines ready to profit from the market you are about to create.
  • Your Pharma-investor sponsors also sponsor disease modelers willing to produce the most fantastic death figures to shore up public compliance. They do this.
  • You then use your powers to impose these lockdowns and insist that a 100-day vaccine must be rushed out to save hapless humanity and allow a return to an “inter-pandemic” period.
  • Once your chosen companies rush out the vaccine, you get to control the regulatory bit (more money changes hands), bypassing pesky safety trials and those interminable ethics reviews.
  • All the while, you can note any dissenting opinions that may reduce your market size; your governmental partners having already agreed to deal with them.
  • Once you have the profit flowing, you get to decide when the profiteering can stop (think “respiratory virus vaccine” and more sponsored modeling – rapid waning of efficacy so lots of boosters to keep humanity safe).
  • All the while, you have ensured freedom from liability for your pharma partners and your own regulatory process.
  • You, of course, have no liability either – you are above any national jurisdiction. You don’t even have to pay tax to anyone!

(See link for article)

________________

**Comment**

I highly recommend reading, “For Some, There is Not Enough Infectious Disease in the World – So They Want to Pay You to Be Infected.”

Within this article you will learn of the egregious violations of human rights that have occurred historically in medical research.  Many state Lyme disease falls into this category as well.

COVID is a perfect example of how these experiments have shaped current ethic standards – or lack there of.  

“They serve as a grim reminder of what can occur when ethical considerations are sidelined for the sake of scientific inquiry or under the guise of political and racial ideologies…..these best practices appear to have all but been forgotten by Vaccine Manufacturers and Public Health.” ~ James Lyons Weiler

In short, a recent Guardian article spotlights Australia’s the Doherty Clinical Trials (DCT), a new facility dedicated to human challenge trials designed to expedite the understanding of diseases and the development of vaccines and treatments by intentionally exposing consenting participants to infectious agents or pathogens in a controlled environment.

The trials, which focus on a variety of diseases, from influenza to malaria and gonorrhea, involve compensating volunteers, typically young adults and travelers, for their participation – demonstrating enticement to consent and potential long-term health impacts.

The article points out glaring problems:

  • lab leaks
  • generation of more virulent or resistant strains of pathogens
  • the rapid deployment and approval of dangerous gene therapy injections falsely labeled as ‘vaccines’
  • the deliberate exploitation of socioeconomic vulnerabilities through financial enticement on populations already marginalized by the healthcare system 
  • risk of long-term chronic illnesses due to the long-term impacts of pathogen exposure – known as pathogenic priming
  • repeated exposures to infection and then injection will likely cause autoimmunity as history has shown

Weiler calls for a ban on human challenge trials which is rooted in the principle of “first, do no harm,” a cornerstone of medical ethics that appears to be all but forgotten.

Category:

Activism, Treatment, vaccines, Viruses

LSU Obtains Grant to Synthesize Affordable Nootkatone

https://www.lsu.edu/eng/news/2024/03/che-nsf-pfi-grant-lyme-disease.php

Chemical Engineering, Biological Sciences Faculty Receive Largest NSF PFI Grant Ever Awarded to LSU

Mike Benton, Kerry Dooley, Roger Laine
Nootkatone Studies Could Lead to Prevention of Lyme Disease

March 25, 2024

BATON ROUGE, LA – Thanks to a $550,000 National Science Foundation Partnership for Innovation grant—the largest NSF PFI grant ever awarded to LSU—LSU Chemical Engineering (ChE) Professor Kerry Dooley, LSU ChE Department Chair and Professor Mike Benton, and LSU Department of Biological Sciences (Biol. Sci.) Professor Roger Laine will continue their work on a project that could bring affordable and effective insect repellent to the masses, possibly decreasing the number of Lyme disease, malaria, and West Nile virus cases around the world.

The project involves the use of nootkatone, an FDA-approved organic compound found in grapefruit skin and Alaska yellow cedar trees that is a natural deterrent for many insects, including the deer tick responsible for Lyme disease. The LSU researchers propose decreasing the cost of the nootkatone synthesis, making any products made with the compound affordable to the general public.

“The family of compounds that make up nootkatone is already proven to be both safer and more effective than existing commercial repellents,” principal investigator Dooley said. “However, it’s now too expensive for consumer insect repellents. We plan to greatly streamline, optimize, and reduce the costs associated with the synthesis.”

According to Laine, there have been few insect repellents on the market since DEET, which is found in most insect repellent sprays and creams currently available. However, a mosquito test showed that nootkatone at 5% in rubbing alcohol was superior to DEET, which usually needs to be administered at greater than 20% concentration, even six hours after application.

Years ago, Laine discovered the efficacy of nootkatone as an insect repellent while collaborating with retired LSU AgCenter Entomologist Gregg Henderson in Laine’s lab. They found that nootkatone repelled insects like mosquitos, gnats, wood ticks, fleas, termites, lice, and fire ants because the insects weren’t eating the vetivone grass that, unbeknownst to them, contained nootkatone. Former LSU Biol. Sci. Senior Research Associate Betty Zhu tested 15 other compounds that resembled the structure of the vetivone and discovered that nootkatone was the best repellent compound. Nootkatone had already been approved by the FDA at the time, with the CDC later discovering that it also repels deer ticks.

Though nootkatone was found to be the best repellent, the problem was the cost to buy it in pure form.

“Nootkatone costs $2,500/kg, which is too costly for insect repellent,” Laine said. “It should be $200-$300/kg, then you can add it to lotions and sunscreens.”

Dooley discovered that one important way to save on the cost would be to modify a step in the eight-step synthesis of nootkatone.

“I did a cost analysis of the synthesis process, and 70% of the cost is concentrated in the fourth step of the eight-step process,” Dooley said. “I decided this step in particular could be significantly reduced in cost.”

The eight-step synthesis was created in just two years by former LSU Chemistry Graduate Student Anne Sauer, who was working under retired professor William Crowe as a collaboration with Laine and Henderson. To simplify two oxidation steps in the eight-step synthesis, which is patented by LSU, Laine subsequently obtained a Board of Regents seed grant and hired synthetic chemist Xuefeng Gao to successfully modify the synthesis using ozone, now covered by new U.S. and Japanese LSU patents authored by Laine.

In the fourth step, the original paper and patent uses potassium hydride and 18-Crown-6 ether, along with tetrahydrofuran, as a solvent. Dooley read up on how people were trying to execute this step without using these expensive components and thought he and Benton should come up with a catalyst and solvent that could significantly reduce the cost of this step.

“It’s incredibly complicated and it takes a long, sustained effort to go from making a few grams of something to making kilograms or kilotons,” Dooley said. “There’s a lot of work on optimizing separations, minimizing the solvent use, getting certain impurities down, and getting yields slightly up. These things take a lot of time and effort.”

The LSU research team hopes to sell their synthesis process to a manufacturing company, who would then be able to mass produce affordable nootkatone products that could save people’s lives by preventing bites from infectious insects.

A 2024 CDC report states that there were 62,551 Lyme disease cases in 2022. Recent estimates using new data collection methods suggest approximately 476,000 people may be diagnosed with Lyme disease each year in the U.S.

“The deer tick is spreading throughout the U.S.,” Dooley said. “It’s not just prevalent in the Northeast.”

In other words, insects are going nowhere. A 2023 CDC report states there were 2,406 cases of West Nile virus across 43 states with the number of cases expected to increase in 2024. Per the World Health Organization, there were a reported 249 million cases of malaria worldwide last year.

“Sixty million people die of malaria each year,” Laine said. “It’s possible that if this eight-step synthesis process could produce nootkatone products that get to poorer countries, then WHO could possibly fund it. Mosquito nets could be covered with it, or they could have cloth ankle bands with nootkatone so ticks can’t crawl up your leg. The Department of Defense is also interested in ways to protect military personnel against tick-borne diseases. There are a lot of marketing niches with this.”

Contact: Libby Haydel
Communications Manager
225-578-4840
ehaydel1@lsu.edu

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Category:

mosquitoes, Prevention, research, Ticks, Treatment

AMA President Opposing Free Speech As COVID ‘House of Cards Collapsing’

https://petermcculloughmd.substack.com/p/ama-president-opposes-free-speech?

AMA President Opposes Free Speech

Dr. Jesse M. Ehrenfeld believes vaccine orthodoxy must be preserved at all costs

JOHN LEAKE
MAR 27, 2024

Dr. Jesse Ehrenfeld was inaugurated president of the American Medical Association in 2023. He and his colleague—Dr. Benjamin Hoffman, an Oregon-based pediatrician—just wrote a very foolish editorial in MEDPAGE TODAY titled: Medical Misinfo Runs Rampant Online. The Gov’t Must Retain the Right to Intervene.—Combating vaccine falsehoods and other inaccurate claims protects public health

According to Dr. Ehrenfeld’s bio that is posted on the AMA website, he has a distinguished career in anesthesiology. His bio also states:

Upon his inauguration, Dr. Ehrenfeld made AMA history as the first openly gay president of the organization. For the past two decades, he has been a nationally recognized advocate for lesbian, gay, bisexual, transgender and queer (LGBTQ+) individuals. In 2018, in recognition of his outstanding research contributions, he received the inaugural Sexual and Gender Minority Research Investigator Award from the director of the NIH.

I’m immediately struck by the combination of anesthesiologist and gay rights activist, as both endeavors have been matters of great controversy since the mid 19th century.

Imagine if—following Friedrich Sertürner’s discovery of morphine in 1805—medical boards in the United States (affiliated with the British East India Company) insisted that ONLY opioid-based analgesics could be used, and that no one could use ether to anesthetize patients. To understand just how much disagreement, discussion, and debate there was around the use of ether, take a look at this history of the Ether Controversy.

Imagine if a medical board in Boston established a censorship apparatus to prevent anyone from challenging the supremacy of morphine as an analgesic, so that William Morton, Crawford Long, and Oliver Wendell Holmes, Sr. couldn’t publish about the value of ether for surgical anesthesiology.

Fast forward to the end of the 20th century. Imagine if no one was allowed to publish any criticism of the promotion and marketing of OxyContin by Purdue Pharma.  (See link for article)

The AMA is entirely corrupt, instructs doctors to deceive, and has caused untold thousands of deaths due to their banning of early treatments for COVID.

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https://expose-news.com/2024/03/27/dr-fullmich-statement-from-prison-their-house-of-cards-is-collapsing/

Dr. Füllmich Statement From Prison – ‘Their House of Cards is Collapsing’

BY  ON 

Dr. Reiner Füllmich has continued to analyze evidence of the crimes against humanity from prison. that he and the Corona Committee had been working to expose since 2020. The corruption is being increasingly seen worldwide and “Their house of cards is collapsing” according to Reiner, “and we as international attorneys will do our best to speed up that process and make sure that Justice is done.” He adds ‘The windows of truth that are opening worldwide and the light that shines through these windows is in the process of identifying all of those who are responsible, no one will escape Justice.‘

Reiner Füllmich made this statement in a a break from the his trial due to the Easter holidays which has followed eight days in court. He has now been able to summarize the criminal proceedings against him and concludes that Hoffman and Antonia Fischer were only interested in ‘getting their hands on the Corona Committees donation. He claims that ‘through ‘fraud and extortion’, they had gotten their hands on roughly 1.5 million euros of his and his client’s money.’

Viviane Fischer, however, has confirmed in court that they both took loans in order to secure the Corona Committee’s donations which were at risk from “government attack, but they were both able to pay the monies back.

What this means is accusations that Reiner had embezzled committee funds are unfounded. In fact, there seems to be no reason for the man to have been kept in jail at all, and he believes, as many others do, that the criminal proceedings are an effort to shut him up and put him in jail and can see that the ‘DA’s case, is dead in the water.’

Reiner therefore, seems to be more positive for the future, which can be heard in his statement which you can listen to in full in the video of the audio below. However, I have also transcribed the audio recording verbatim and have added it underneath the video for those unable to play videos. (See link for article and 10 Min video)

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Category:

Activism, Treatment, vaccines, Viruses

Ivermectin Win: FDA Must Remove Controversial Verbiage From its Website While DOJ Attempts to Shut Down Pfizer Fraud Case

**UPDATE**

Besides bad-mouthing ivermectin, a U.S. government ‘cartel’ bribed large pharmacy chains like Walgreens and CVS with billions of dollars in contracts to promote COVID-19 vaccines and not fill prescriptions for ivermectin.  See:  The FDA’s War Against America’s Health

https://petermcculloughmd.substack.com/p/breaking-dr-mary-talley-bowden-reacts

Agency Capitulates by Removing False Claims on Ivermectin from Social Media and Internet

MAR 25, 2024

By Peter A. McCullough, MD, MPH

Thursday evening March 21, 2024, in an unprecedented court case, the US FDA led by  Commissioner Robert Califf, MD, a previously respected Duke Cardiologist, has settled a court case and taken down all of its false and misleading claims on ivermectin. The drug has been part of community standard of care for the treatment of COVID-19 with an excellent safety profile and signals of benefit in 101 studies.

During 2021, in what has been called “A War on Ivermectin” the US FDA engaged in false and misleading tweets and public messaging to dissuade doctors, pharmacists, and patients from using the drug in The McCullough Protocol and similar multi-drug regimens for acute COVID-19.  (See link for article and video)

According to an Epoch Times article , a court ordered the FDA to walk-back its negative posts about using ivermectin for COVID:

  • Studies show ivermectin works against COVID the FDA itself cites, but it’s webpage currently states it is not authorized or approved for use in preventing or treating COVID.
  • The court settlement requires the FDA to delete multiple social media posts that are strongly against ivermectin.
  • For doing this, doctors who sued the agency are dismissing their claims.
  • According to one of the doctors who sued, “This landmark case sets an important precedent in limiting FDA overreach into the doctor-patient relationship.”
  • Another ivermectin prescribing doctor who saw lives saved states that due to FDA interference, “we will never know how many lives were affected because patients were denied access to a lifesaving treatment because their doctor was ‘just following the FDA.’”
  • The three-judge panel of the U.S. Court of Appeals for the Fifth Circuit found that the law did not authorize the FDA to give medical advice.
  • Numerous doctors have chronicled the highly coordinated and timed actions between the FDA, CDC, AMA, APHA, and corporate controlled media to squash ivermectin – an extremely safe, cheap drug on the WHO’s essential list of medicines that has been used for decades without a prescription in many countries, including Africa which had essentially ZERO COVID due to the prolific use of the drug.

“FDA can inform, but it has identified no authority allowing it to recommend consumers ‘stop’ taking medicine,” U.S. Circuit Judge Don Willett, wrote for the court. The appeals court remanded the case back to the district court.

Predictably, the FDA didn’t get the memo:
  • and has not “admitted any violation of law or any wrongdoing, disagrees with the plaintiffs’ allegation that the agency exceeded its authority in issuing the statements challenged in the lawsuit, and stands by its authority to communicate with the public regarding the products it regulates.”
  • and has not changed its position that currently available clinical trial data do not demonstrate that ivermectin is effective against COVID-19. The agency has not authorized or approved ivermectin for use in preventing or treating COVID-19.”
Welcome to the Twilight Zone.

For a quick flashback, watch this video of a doctor being forcibly removed by police from a hospital board meeting simply for endorsing ivermectin that he used in his own private practice, and for evidently breaking protocol by whispering a “thanks” to a politician who questioned hospital policy. He shared at about 7:00 that doctors on staff at the hospital would come and see him to get ivermectin but would not speak their mind or prescribe it for fear of retribution from hospitals or their own medical groups. He states that 99% of doctors now have a contract with the hospital and are beholden to it, and that ‘brutal’ COVID treatment protocols, which one nurse blamed for 90% of hospital deaths, were followed to the letter due to government financial incentives.  Hospitals were simply not interested in early treatment which have saved lives and freed up hospital beds.

This video shows how the CARES Act signed into law in 2020 waived patient rights, and made hospitals rich (approx. 100K per COVID patient) due to these government incentives.

The ivermectin-prescribing doctor was unable to eat in the hospital employee lounge because he didn’t take the COVID shot.

And the reason the suit was brought in the first case was due to doctors suffering repercussions after prescribing ivermectin to patients with COVID.  Pharmacists refused to fill prescriptions.

The FDA is certainly guilty, as well as other government agencies.  But so are hospitals, medical groups like the AMA, APHA, ASHP, mainstream media, and doctors themselves.

Unless action is taken, this can and will happen again.

________________

https://www.naturalnews.com/2024-03-22-department-of-justice-intervenes-pfizer-fraud-case.

Collusion coverup: Department of Justice intervenes in Pfizer fraud case, in a corrupt attempt to shut the case down

03/22/2024  Lance D Johnson
Story at a glance: (summary by “Neo” LLM via Brighteon.AI)- The United States Department of Justice (DOJ) is attempting to shut down the Pfizer fraud case scheduled for April 17.- The lawsuit alleges that Pfizer-BioNTech violated the False Claims Act during their clinical trials and knowingly delivered a defective product to the world.- Former employee Brook Jackson, who worked at Ventavia Research Group (a company that conducted some of Pfizer’s COVID-19 vaccine clinical trials), is suing Pfizer, her former employer Ventavia, and another Pfizer contractor, ICON plc.- The DOJ asked the court to dismiss the lawsuit, claiming it would be inconsistent with their public health policy.- The DOJ’s motion to dismiss cites a flimsy hypothesis authored by the FDA, which supports the faulty vaccines and contradicts Jackson’s claims of fraud and negligence.  (See link for article)

Pfizer sunk to unbelievable lows to peddle their gene therapy shots including using children in ads
The shot not only flopped, it caused more COVID infections & an inflammatory syndrome

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Category:

Activism, Cancer, Treatment, vaccines