Author Archive

ACTION: FDA Closing in on Your Supplements

https://anh-usa.org/fda-closes-in-on-your-supplements/

FDA Closes in on Your Supplements

By ANH-USAOn 
FDA Closes in on Your Supplements
The agency recently made a big announcement about a regulation that could eliminate 41,700 products from the market. We need to keep up the pressure to protect access. Action Alert!

THE TOPLINE

  • The FDA announced that it will release the final version of the “new dietary ingredient” (NDI) guidance in several distinct pieces.
  • This is deeply concerning because 1) it shows the extent of the focus the agency wants to dedicate to this guidance, and 2) it prolongs the uncertainty regarding NDI notification procedures, increasing the chances that Big Pharma can use the FDA’s back-channel to steal more natural products.
  • It is increasingly looking like the FDA is following in the footsteps of the European Union’s restrictive supplement regulations in order to create a harmonized, global market.

A few weeks ago, we reported that 2024 could be the year the FDA finally publishes the final version of its natural product-destroying “new dietary ingredient” (NDI) guidance that it has been working on since 2011. It appears that we might have been right. On January 17, the FDA published a notice in the Federal Register explaining that it intends to break this up into several guidance documents while also naming the issues it intends to prioritize. It is a tactic we’ve seen the agency deploy in its war against compounded medicine: rather than issue a policy outright and risk the backlash, the FDA takes a piecemeal approach to diffuse the negative reactions to what it is doing. Even more concerning, it shows the level of focus the FDA is committing to the various issues contained in the guidance. We need to keep hammering away at our elected representatives to take notice of what the FDA is doing.

The Federal Register notice states that the issues FDA is prioritizing are administrative procedures, identity, safety, and master files. The FDA’s webpage describing the guidance documents it plans to issue over the next year has been updated accordingly, with a “procedures and timeframes guidance” listed before a master files guidance.  (See link for article to to take action)

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Activism, Supplements

ALS & MS Suspected in Woman Later Diagnosed With Bartonella & Lyme Disease

https://danielcameronmd.com/als-and-ms-suspected-in-woman-later-diagnosed-with-bartonella-and-lyme-disease/

ALS AND MS SUSPECTED IN WOMAN LATER DIAGNOSED WITH BARTONELLA AND LYME DISEASE

bartonella-lyme-disease

After developing multiple neurologic symptoms following a spider bite, a woman tests positive for Bartonella. Yet, her symptoms are attributed to possible multiple sclerosis (MS) or ALS. Just prior to having hip surgery, additional tests confirm that she is positive not only for Bartonella, but for Lyme disease, as well.

By 

In their article, “Bartonella- and Borrelia-Related Disease Presenting as a Neurological Condition Revealing the Need for Better Diagnostics,” Ericson and colleagues describe the case of a 61-year-old female, who experienced a painful bite while hiking in Minnesota.¹

It was diagnosed as a spider bite because of the two large bite marks present and the painful sensation. One day after the bite, a large blue ring appeared around the bite and the woman developed muscle aches and pains.

The woman was treated with doxycycline for two weeks, which decreased but did not resolve the arthritic pain.

Five months later, her symptoms progressed to include blurry vision, lack of balance, muscle pain, night sweats and insomnia.

At this point, testing for Lyme disease and Bartonella were negative.

After expressing continued concern about having Lyme disease, she was referred to an infectious disease physician, who stated that he “did not believe in persistent Lyme disease.” She was then referred to a neurologist for an MRI.

“At this time, her blood was used in a research study aimed at developing new PCR diagnostic techniques for Bartonella infections,” the authors state.

This new PCR test confirmed the presence of both Bartonella vinsonii and Bartonella henselae.

One year after infection, the patient visited an integrative medicine physician who prescribed clarithromycin and rifampin based on symptoms consistent with a Bartonella infection.

However, her symptoms continued and she was referred to a physical therapist, who prescribed a wheeled walker. Her primary care physician attributed her symptoms to possible ALS or MS.

“She reported to multiple physicians that her hips sounded like popcorn whenever she walked or climbed stairs.”

Hip x-rays revealed a loss of cartilage. She had bilateral hip degeneration, which would require hip replacements.

Prior to surgery, the woman underwent another round of tests for Bartonella. And again, test results confirmed for a second time the presence of Bartonella.

However, in addition, testing revealed “a spirochete-like organism” in a buffy coat smear sample.

“Given her symptomology and the known possibility of co-infections in Lyme disease, the spirochete was suspicious for Borrelia burgdorferi.”

Testing for Lyme disease was positive.

Once the woman began treatment for Lyme disease, her condition improved.

However, “Despite the intermittent use of antibiotics for five years, the patient remains positive for Bartonella henselae and Borrelia burgdorferi.”

If she ceases taking antibiotics, her symptoms recur within 3 months.

Authors Conclude:

  • “This case report illustrates the inadequacy of conventional tests in diagnosing Bartonella spp. infections, and the potential promise of enhanced techniques.”
  • Serology and other antibody-based tests are usually used for Bartonella and Borrelia detection. However, this patient never tested positive through serology but was positive by FISH and PCR testing.
  • “The limitations of serology for detecting an active infection need to be more clearly understood by the medical community.”
References:
  1. Ericson ME, Mozayeni BR, Radovsky L, Bemis LT. Bartonella- and Borrelia-Related Disease Presenting as a Neurological Condition Revealing the Need for Better Diagnostics. Microorganisms. 2024; 12(1):209. https://doi.org/10.3390/microorganisms12010209

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**Comment**

Incredible work here, and it’s easy to see why: the funding for it was independently obtained through the Steven & Alexandra Cohen Foundation and all the authors are serious researchers who are not part of the Cabal.  I know three of them personally and Dr. Mozayeni is a widely known and respected LLMD.  This work would NEVER happen in mainstream research which is completely bought out and untrustworthy.  Ericson, whose son had a severe Bartonella infection, continues to do amazing work:   https://madisonarealymesupportgroup.com/2019/02/27/advanced-imaging-found-bartonella-around-pic-line/

This study shows perfectly what patients have been up against for decades: negative serology, coinfection involvement making the CDC definition meaningless, and transmission by other insects and arachnids.

But, nobody will care about this work except patients and the doctors who dare to treat them.

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Category:

Bartonella, Lyme, research, Testing, Treatment

Moderna Scientists Admit mRNA Drugs Have Toxicity Risks & Leaked AstraZeneca Audio Recording

Dr. Yeadon warned about this toxicity over two years ago.

These are “toxic by design”. It cannot be an accident.  ~ Dr. Yeadon

Brave doctors, researchers, embalmers, funeral directors and even paramedics continue to expose what they are seeing, and to implore people not take the mRNA gene-therapy injections.

https://www.nature.com/articles/s41573-023-00859-3

Strategies to reduce the risks of mRNA drug and vaccine toxicity

Dimitrios Bitounis, Eric Jacquinet, Maximillian A. Rogers & Mansoor M. Amiji

Nature Reviews Drug Discovery (2024)Cite this article

Abstract

mRNA formulated with lipid nanoparticles is a transformative technology that has enabled the rapid development and administration of billions of coronavirus disease 2019 (COVID-19) vaccine doses worldwide. However, avoiding unacceptable toxicity with mRNA drugs and vaccines presents challenges. Lipid nanoparticle structural components, production methods, route of administration and proteins produced from complexed mRNAs all present toxicity concerns. Here, we discuss these concerns, specifically how cell tropism and tissue distribution of mRNA and lipid nanoparticles can lead to toxicity, and their possible reactogenicity. We focus on adverse events from mRNA applications for protein replacement and gene editing therapies as well as vaccines, tracing common biochemical and cellular pathways. The potential and limitations of existing models and tools used to screen for on-target efficacy and de-risk off-target toxicity, including in vivo and next-generation in vitro models, are also discussed.

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http://  Approx. 7 Min

White Clots in Bodies of COVID Jabbed

Dr. John Campell presents data from Major Thomas Haviland’s Worldwide Embalmer Blood Clot Survey:

  • in 2023 embalmers report 20% of corpses had reporting white, rubbery clots
  • in 2022 30% had them
  • in 2021 there were quite a lot, but they didn’t collect a figure
  • in 2020 before the COVID shot rollout, there were very few cases
  • in 2019 none were seen
These clots are new and are not presented in any pathology textbooks.

Campbell asks the important question: Why isn’t this all over mainstream media and the scientific literature?

He also states “We need answers, and we need a moratorium until we get those answers.”

Yet, Bill Gates aka ‘Bat Man,’ is proud of these mRNA clot-shots and continues to peddle them with abandon.

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https://sashalatypova.substack.com/p/audio-leaked-from-astrazeneca-covid

Audio recording leaked from AstraZeneca

Recorded at an internal executive meeting at the end of 2020. This recording has not been published previously anywhere.

SASHA LATYPOVA
FEB 7, 2024
Important Excerpts:

The audio confirms that the DOD pandemic pharma consortium was established in 2017 and the DOD, (not pharmas) was, and remains in charge of it. I knew this based on the covid contracts analysis, but it’s good to have a definitive confirmation. The AZ execs are musing that at the time they thought the DOD’s pandemic preparedness plan – from “discovering” new viruses to making new drugs for them in 60 days – sounded like science fiction. That’s because it is science fiction, even though I am sure most people involved in it believe their own insane delusions. It appears that the DOD money was very green and quickly dulled the skepticism of AZ execs. The CEO of AstraZeneca, Pascal Soirot is on record stating that millions of people in the world cannot be vaccinated by mRNA shots because they have autoimmune conditions and other vulnerabilities. They always knew.  (Go to link for audio, article, and transcript)

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Category:

Activism, research, vaccines

WHO Whines About ‘Fake News’ As Pandemic Treaty Goes on Life Support

http://  Approx. 27 Min

The World Health Organization’s Dark Agenda

Tucker Carlson and Bret Weinstein discuss the World Health Organization’s dark agenda which will come to pass if nations sign onto the ‘Pandemic Treaty.’

  • We are in the middle of a coup and risk losing our national and personal sovereignty.
  • In May of this year, nations will choose whether or not to sign into this far-reaching, global legislation that will affect every aspect of life.
  • Nations who sign it will cede all power to the Director General to the WHO
  • The WHO can declare a public health emergency on any basis
  • They can then mandate remedies (vaccines, gene therapy technology, ability to travel, they can forbid any treatments they want, and they can censor anything they wish, etc.)
  • The Department of Homeland Security came out with a memo describing three types of terrorism: misinformation (errors), disinformation (intentional errors or lies), and malinformation (things that are based in truth but cause you to distrust authority).  Terrorism is a legal designation that evaporates all your rights.
  • COVID made us aware of the “turn key” totalitarian planet (totalitarian built structures around us that only need to be activated by a “key”)
  • ‘The powers that be’ are capitalizing upon a ‘pandemic’ as a loophole to bypass our rights, despite our Constitution not making a provision for this.
  • Weinstein feels the US government wants this WHO takeover in order to violate our Constitutional rights. Go here to learn about “The Great Reset,” which is a multi-pronged, global effort of which the attack against health/medicine is only one facet.
  • The good news is the Eastern block is much less ready to adopt the treaty, but Weinstein worries it will be too thin and too little.  The world is now depending upon them to resist, as the US is compromised.
  • All eyes are on Ireland as well as the government cannot enter into a pandemic treaty without a referendum due to the Crotty ruling precedent.
  • Please note that Wisconsin is a state with bills that point to the WHO as experts.
  • A recently unearthed video of Yuval Noah Harari, WEF mastermind who is a perfect example of the type of thinking behind the global takeover, explains to the crowd why he believes “useless humans” should have no rights.  He claims these rights are fiction.
  • An elite cadre of leaders, molded within the corridors of Davos and the classrooms of the Young Global Leaders (YGL) program, has ascended to pivotal roles in governments, corporations, civil society organizations, and global agencies like the WHO, wielding considerable sway over the direction of global policy and governance.
  • Greg Reese’s 5 minute video details how the U.S. implemented a plan a long time ago for this global New World Order.

Contact your representatives and tell them we should cut the head off the WHO, WEF, Gavi and UN snake.

Rep. Chris Smith (R-NJ), Chairman of the House Subcommittee on Global Health, Global Human Rights & International Organizations, and who previously attempted to get to the bottom of the bioweaponization of Lyme Disease, held a press conference where he said there has been “far too little scrutiny” of and “far too few questions asked” about what the World Health Organization’s (WHO) “pandemic treaty” will mean to the United States.

Smith is also concerned whether the Biden administration will submit the so-called “treaty” to the U.S. Senate “for its constitutionally-required advice and consent as a prerequisite for ratification,” warning that “an executive agreement bypassing Senate ratification would be an egregious mistake.”

He drew attention to Article 18 that seeks to “combat false, misleading, misinformation or disinformation.”

“Will there be any room for dissent on vaccines, therapeutics, virus transmission and the like—especially among scientists and health professionals—or will group think again crowd out other viewpoints?” the congressman asked. “We have reason for concern—past could be prologue.”  Source

https://thehighwire.com/ark-videos/pandemic-treaty-on-life-support-as-public-trust-plummets/  Video Here Approx. 14 Min

WHO Whines About ‘Fake News & Conspiracy Theories’ But Continues to Lie

The WHO, WEF, and legacy media are lamenting the lack of trust they are now experiencing by the public. We provide evidence for where exactly the fault for their lack of trust and popularity lie.

POSTED: February 2, 2024

Worldwide protests are continuing, despite MSM’s silence. The opposition is real and growing.  The video at 3:15 discusses the FDA’s continued tyranny against supplements including NMN, a safe antioxidant and precurser to NAD+, they wish to redesignate as a drug, allowing Big Pharma to corner the market.

Speaking of cornering the market, the video also highlights the EU’s actions that have made it impossible for European farmers to sell their own crops, due to Ukraine’s cheap imported products that may not even meet food safety standards.  The EU’s insistence upon “Net Zero,” and other arbitrary rules that cost farmers have hog-tied them.  As this video points out, “Going Green tends to reduce food availability and increase their costs.” 

The U.N. is ‘secretly working with banks’ to destroy the American food industry. The banks are using the UN’s Marxist “environmental, social, and corporate governance” (ESG) criteria to score and penalize farmers.  From 2020-2022 there were nearly 100 fires in food facilities making some question if we are experiencing food sabotage.

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Category:

Activism

Fluoride on Trial: Federal Trial on Neurotoxicity of Water Fluoridation

Brian Berridge, DVM, Ph.D., the former scientific director of the National Toxicology Program (NTP) took the stand on the fourth day of a landmark trial on water fluoridation, despite efforts by the U.S. Environmental Protection Agency (EPA) to scuttle his testimony. He testified about the initial findings in the NTP’s draft report linking fluoride to lower IQ in children.

He also spoke with The Defender about the fact that to protect their existing practices public health officials are ignoring the fact that many are exposed to high fluoride levels.  This is also an ongoing problem with vaccines and the fact that to date nobody has tested the accumulation of metals and adjuvants that occurs over time due to multiple vaccines.

Ninety seven percent of Western Europe has rejected water fluoridation.

https://www.einpresswire.com/article/683819418/fluoride-on-trial-federal-trial-on-the-neurotoxicity-of-water-fluoridation-resumes-next-week

Plaintiffs Ask Federal Court to Ban Fluoridation Chemicals in Upcoming Ruling

SAN FRANCISCO, CALIFORNIA, U.S.A., January 25, 2024 /EINPresswire.com/ — After nearly four years of delay, a lawsuit in United States federal court seeking to prohibit the addition of fluoridation chemicals to public water systems due to the threat posed by fluoride to the developing brain is set to continue next week, reports the Fluoride Action Network (FAN).

The final phase of the landmark bench trial against the U.S. Environmental Protection Agency (EPA) over the neurotoxicity of fluoridation chemicals will start on Wednesday, January 31st, 2024. The U.S. District Court, Northern District of California in San Francisco, has set aside nine days (January 31, February 1, 2, 5, 6, 7, 9, 12, 13) for testimony and cross-examination of expert and fact witnesses.

The focus of this final phase will be on the new evidence and science published since the last trial dates held in 2020. This will include the National Toxicology Program’s (NTP) 7-year systematic review of the neurotoxicity of fluoride. Specifically, fluoride’s impact on reducing the IQ of children. The NTP reported that 52 out of 55 fluoride brain studies they looked at found decreases in child IQ associated with an increase in fluoride, a remarkable 95% consistency. Of the 19 studies rated highest quality, 18 found a lowering of IQ. The meta-analysis could not detect any safe exposure, including at levels common from drinking artificially fluoridated water.

The Fluoride Action Network (FAN), a non-profit founded in 2000, is the lead plaintiff in this precedent-setting case, which challenges a practice endorsed by the U.S. Public Health Service 75 years ago and that today affects more than 200 million Americans through water fluoridation systems in thousands of communities. FAN is joined by consumer advocacy groups, Food and Water Watch and Moms Against Fluoridation, public health associations, the American Academy of Environmental Medicine and the International Academy of Oral Medicine and Toxicology, as well as several individuals representing themselves and/or their children. The case is number 17-CV-02162-EMC (KAW), and titled: Food & Water Watch, Inc., et al. v. United States Environmental Protection Agency, et al.

The lawsuit falls under the Toxic Substances Control Act of 1976 (TSCA) which gives EPA the authority to prohibit “the particular use” of a chemical substance if it presents an unreasonable risk to the general public or susceptible subpopulations. The plaintiffs submitted a Citizens Petition under Section 21 of TSCA to the EPA in November 2016 requesting a ban on the addition of fluoridation chemicals to water. When the EPA denied their Petition, they filed suit in federal court.

Click here for a timeline of the lawsuit.

“There’s no question that the weight of the science overwhelmingly shows that fluoride damages the developing brain,” said Stuart Cooper, FAN Executive Director. “This includes a large body of government-funded research indicating that fluoride is neurotoxic, is associated with lowered IQ in children, and a significant increase in ADHD diagnosis and related behaviors in children at doses experienced in fluoridated communities. Experts in toxicology have likened the size of the effect to that of lead.”

Broadcast of Trial

The trial will take place in San Francisco with attorneys from the U.S. Department of Justice, representing the Environmental Protection Agency, and attorneys for the Plaintiffs both attending in person. One of the EPA’s witnesses will testify via deposition video with the remainder testifying in person. All proceedings will also be live streamed daily on the court’s Zoom and recorded and posted publicly on the court’s website as part of the Cameras in the Courtroom program. Exhibits will be displayed electronically at trial and on the live stream to allow for a more efficient display of evidence. The judge said that access to this trial was in the public’s best interests.

Zoom info and official court schedule

Trial days will begin at approximately 8:30 a.m. (Pacific) and end at 1:30 p.m. Each side shall have approximately 18 hours to present their case. This includes opening statements, direct and cross-examinations, and closing arguments.

Stuart Cooper
Fluoride Action Network
stuart@fluoridealert.org

Lead attorney for the Plaintiffs, Michael Connett of Waters Kraus and Paul recently discussed the case and science involved at length in an interview:

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Category:

Activism, Dentistry, research