Sandra Finley

Jul 012025
 

With thanks to D.

Morning Sandra

The below article came in today from Dr. Robert Malone.  This is the main reason that ostriches must die, and the thought of natural immunity must die with them. Anything and everything that might expose the hoax that we have lived through the last 5 years must be stopped!

Take a look at the below, and Dr. Malone hasn’t even touched their plan of “Total Control” yet!     D.

From: Robert W Malone MD from “Who is Robert Malone” <rwmalonemd@substack.com>
Sent: Thursday, May 15, 2025    ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏    ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏       ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏      ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­

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The mRNA Drug Industry Strikes Back

A Case Study in How Regulatory Capture Happens

Robert W Malone MD, MS
May 15

 

READ IN APP

Know your enemy.

Today’s essay focuses on the emerging mRNA drug industry, the DC-based lobbying organization that has been formed to support it, push its agenda and interests, and the DC allies that it is cultivating. This industry is the result of massive US government spending, advocacy, subsidies (both financial and regulatory), and promotion through propaganda and censorship. This industry spans academia through small biotech to large Pharma, and of course, big finance and Wall Street. To date, it has been enormously profitable. Like an insatiable spoiled child, it wants still more goodies.

Quoting Secretary Kennedy (May 14, 2025) “When I was a kid, NIH was the premier gold standard scientific institution in the world. Over the years, it was captured by industry.”

By taking the time to understand the “Alliance for mRNA Medicines”, its agenda and interests, how it is being built, and watching as it develops and deploys its propaganda and influence campaign seeking to influence President Trump, as well congressional members, you will gain insight into how the Pharmaceutical Industry has captured NIH, CDC, and FDA. Consider this a case study.

Lately, it has become quite the trendy thing for a subset of MAHA influencers to promote the narrative that the Trump administration is not serious about addressing the widespread malfeasance and harms associated with the COVID genetic “vaccine” products, and in particular, the pseudo-mRNA-based products.

In stark contrast to this divisive and counterproductive narrative, the new mRNA Drug academic-industrial complex is using terms like “existential threat” (ergo, threat of death to the industry) consequent to the appointments of new HHS leadership. In other words, influencers on one side are complaining that not enough is being done fast enough, and on the other side, this new industry seems to be running around saying that the sky is falling.

“This is an existential threat,” according to AMM executive director Clay Alspach, a principal at Leavitt Partners, a health-care consulting firm in Washington DC

Leading the response to this perceived threat to the emerging mRNA drug industry is the new trade industry organization called the Alliance for mRNA Medicines (AAM), which was formed in November of 2023. This lobbying and advocacy organization is headed up by Registered Lobbyist and Foreign Agent Mr. Clay Alspach, a principal at Leavitt Partners, a health-care consulting firm based in Washington DC.

The following is from Mr. Alspach’s corporate bio:

clay.alspach@leavittpartners.com

Former chief health counsel for the U.S. House of Representatives Energy and Commerce Committee.

Clay Alspach is a principal based in Washington, D.C. Clay specializes in health care policy and advocacy related to the Food and Drug Administration, health information technology, Medicare Parts B, C, and D, Medicaid, private health insurance, and the Affordable Care Act.

Prior to joining Leavitt Partners, Clay served as Chief Health Counsel for Chairman Fred Upton of the U.S. House of Representatives Energy and Commerce Committee. During seven years with the committee, he managed, provided strategic direction, and served as the principal representative for the committee on all of its health care-related work. Clay spearheaded legislative initiatives that successfully reformed the SGR (MACRA), reauthorized FDA user fees (FDASIA), and established a national system for drug supply chain security (Drug Quality and Security Act). Clay also led the committee’s legislative accomplishments on biopreparedness and security, public and private medical research, controlled substance and DEA matters, and several other public health initiatives. Most recently, Clay led the committee’s work on the 21st Century Cures Act.

According to Legistorm, Clay Alspach, whose full name is Robert Clayton Alspach, has been registered as a lobbyist/foreign agent. In DC parlance, the term “hired gun” might be used to describe Mr. Alspach’s role in this endeavor.

In case you were wondering what companies and academic organizations consider themselves to belong to this new industry, below is the list, each hot-linked to further information. Notably absent are the University of Pennsylvania, Moderna and Pfizer. This lobbying organization currently employs at least 23 people.

A few weeks ago, I was contacted by a reporter from Nature (Elie Dolgin), who asked to speak to me about a new article he had been commissioned to write. With more than a bit of trepidation, I decided to talk to him. To my surprise and relief, my impression was that Mr. Dolgin was doing real journalism and was seeking some balance of opinion in his investigation.

This article was the result of his labors. Based on my prior experience many years ago working as head of business development for an early Bill and Melinda Gates-funded “non-profit” (Aeras Global TB Vaccine Foundation), I suspect that somehow the Alliance for mRNA Medicines provided support or incentive for Nature to publish this article.

Quoting from the Nature magazine news feature article, which you can read here:

The day after Donald Trump moved back into the White House in January, he celebrated a US$500-billion private-sector investment in artificial intelligence (AI) with a high-profile announcement in the Roosevelt Room. The new president looked on as technology billionaire Larry Ellison highlighted one of the initiative’s most transformative goals: using messenger RNA vaccines to transform cancer treatments.

By harnessing AI to analyse tumour genetics, Ellison explained, researchers could rapidly design personalized vaccines tailored to an individual’s cancer. “This is the promise of AI and the promise of the future,” he said.

Biotechnology executives were elated. Trump had, just five years earlier, propelled mRNA medicines into the spotlight through his signature effort to fast-track the development of a coronavirus vaccine. Now, just one day into his second term, he was once again elevating the technology to the national stage.

“Then the bottom fell out,” says Deborah Day Barbara, co-founder of the Alliance for mRNA Medicines (AMM), a trade group representing more than 75 companies and academic institutions that are advancing mRNA research, development and manufacturing.

A prominent vaccine critic who had vilified the mRNA-based COVID-19 jabs, Robert F. Kennedy Jr, was appointed to lead the country’s top health agency, and long-time champions of immunization science in the civil-service sector were shown the door. Research grants tied to HIV prevention and pandemic preparedness were abruptly cancelled, including many involving mRNA. And numerous other projects that were focused on mRNA vaccine technology were compiled into a list, potentially signalling their impending termination.

At the same time, legislators in several states have been pushing to ban or restrict the use of mRNA-based medicines for infectious diseases. None of these measures has become law, but the efforts threaten to destabilize the mRNA industry, creating uncertainty and potentially limiting patient access to emerging treatments.

The anti-mRNA sentiment — coupled with the sweeping shake-up of science funding across the United States — has sparked fears that this once-celebrated technology, widely seen as a major engine of next-generation vaccines and therapeutics, could soon find itself on the chopping block.

For AMM executive director Clay Alspach, a principal at Leavitt Partners, a health-care consulting firm in Washington DC, the message has been unmistakable: “This is an existential threat,” he says.

By mid-March, the AMM was holding regular conference calls to strategize. Members swapped intelligence, compared notes on delayed grants and tried to anticipate what might come next. Amid the uncertainty, a few questions loomed large: how far would the clampdown on mRNA go? Would it stop at COVID-19 jabs? Would it extend to all vaccines in development for influenza and other infectious threats? Or reach even into mRNA-based drug therapies in the works for cancer, autoimmune disorders, rare genetic diseases and more?

The initial meeting of the AAM has already been completed, and was held November 13–15, 2024 in Boston, MA. Notable keynote speakers included the two senior FDA personnel with direct regulatory responsibilities relating to this industry.

The second annual meeting is now scheduled for September 16-18, 2025
at the Coronado Island Marriott Resort and Spa, 1500 Orange Ave, Coronado, CA. You can find further information concerning this meeting here. Per AAM, the scope and structure will be as follows:

The Alliance for mRNA Medicines (AMM) brings together senior executives and top decision-makers in the mRNA industry to advance pioneering research into vaccines and therapies for patients.

The annual meeting, AMM ASCENT (Advancements in mRNA Science, Commercialiation, Education, and Novel Technologies), features one-on-one partnering opportunities for companies and investors, dedicated networking, keynotes and fireside chats featuring KOLs and industry visionaries, as well as engaging plenary and panel discussions among biotech, pharma, and academic leaders.

The AAM held lobbying meetings on Capitol Hill during September 2023. This AAM “sizzle reel” attached below documents that, at that time, they met with Director, Center for Biologics Evaluation and Research (FDA) Dr. Peter Marks, Louisiana Senator Bill Cassidy, and Kentucky Congressman Brett Guthrie.

Readers of this substack are familiar with the vaccine-industry-friendly concessions extracted from HHS Secretary Kennedy during the Senate Confirmation process by Senator Cassidy, and with the central role that Dr. Peter Marks has played in expediting and defending the mRNA platform and COVID “vaccines”.

Brett Guthrie is the U.S. Representative for Kentucky’s 2nd congressional district. He has not held a specific policy position related to mRNA. However, he has been involved in discussions and legislation regarding healthcare and medical policies, including those that could affect healthcare providers and pharmaceutical companies involved in mRNA technology. For instance, he has been pushing for changes to Medicaid, which could impact the funding and availability of medical treatments and technologies, including mRNA-based therapies.

We should all be asking Senator Cassidy and Congressman Brett Guthrie whether their campaigns or affiliated political action committees have accepted any funding or support from the AAM. And specifically asking Senator Cassidy whether AAM lobbying influenced his actions during Secretary Kennedy’s confirmation process. The Senator’s contact information is linked above.

FDA Guidance for Industry Benefits the mRNA Drug Industry

During May 2024, the FDA issued a draft guidance for “Platform Technology Designation Program for Drug Development” which you can review here. The AAM sees this new regulatory position as a great opportunity for the mRNA drug development industry and has developed a summary of its analysis, which can be viewed here.

In a virtual meeting presentation focusing on the new FDA platform technology guidance, the Alliance for mRNA Medicines discussed the potential of mRNA product development, the benefits of platform technology, and the challenges associated with mRNA delivery. The panelists also discussed the implications of the FDA’s draft guidance on platform technology designation, the potential of using a platform technology for various applications, and the need for broader understanding of who could be the sponsor. The conversation ended with an invitation for further discussions and the announcement of the registration for the annual meeting of the Alliance for mRNA Medicines.

Sara Singleton, Managing Director of the Alliance for mRNA Medicines, welcomed attendees and outlined the agenda for the webinar. The speakers included Andrew from Replicate Bioscience, Alana Goldberg from Replicate, Dave Schmickel from CSL, Bearing, Yi Zhang from Arcturus Therapeutics, and Sean Semple from Acuitas Therapeutics. The webinar aimed to discuss the history of mRNA product development, the promise of mRNA as a platform, the FDA’s platform designation program, delivery technology, and AMM’s comments on the FDA’s draft guidance. The meeting also covered the implications for the future of product development and mRNA. Development of this guidance was required by the Congressional Pandemic Act of 2022. A transcript of this webinar, which includes insights into the current status of the industry and products in the pipeline is available at this link.

Top AAM Policy Lobbying Focus and Issues

Let’s take a look at the top policy issues and agendas that the AAM will be lobbying to address and advance.

AMM advisors plan to engage with governments, policymakers, regulators, and other stakeholders in North America, Europe, and Asia Pacific to advocate for the following policies that AAM asserts will encourage innovation, define regulatory standards, support manufacturing, and promote access of mRNA medicines to patients.

The text cited below has been lightly edited to remove misspellings.

Regulatory framework for vaccines and therapeutics

To realize the promise of mRNA across its many potential applications, AMM believes regulators should develop a specific regulatory framework for mRNA Why? The areas in which the field needs clarity for mRNA development and manufacturing are different than the issues most pressing for small molecules and other biologics (including cell and gene medicine). The development of a specific framework for mRNA would provide certainty for the community as well as help FDA as it they consider issues from pre-clinical to post-approval.

This regulatory environment would enable continued flexibility and speed in development of mRNA vaccines and therapeutics around the world.

AMM is also promoting international harmonization and cooperation among regulatory authorities across the globe to propel mRNA technology forward in all its potential uses and to move smoothly between discovery, development and deployment stages.

Interpretation: Essentially, AMM is striving to establish a globalized, frictionless business model for mRNA development, enabling them to expand into a worldwide market for their products. They are using the regulatory process to achieve this goal.

Standards Development

With some of the most recognized innovators in mRNA, AMM will help overcome the obstacles to mRNA medicine development stemming from uncertainty about standards. We are convening our members and partnering with relevant organizations to develop, where needed, or improve upon standards for the field.

Interpretation: Regulatory standards benefit large corporations, as a strong regulatory environment captured by big business keeps the competition at bay.

Education (combating mRNA vaccine misinformation and explaining mRNA therapeutics)

AMM is playing a role in combating mRNA vaccine misinformation and demystifying the technology by explaining how mRNA works. We are educating policymakers, payers, and the public about the great potential of mRNA across many different applications so that as they move from bench to bedside, there is greater awareness of it.

Interpretation: This is all about getting the government, insurance companies, and hospitals to foot the bill for these new products.

Access

As more mRNA based therapies and vaccines are developed, AMM will lead the field in communicating to government and private sector payers on access issues to ensure patients receive the benefits of these products.

Interpretation: Again, this agenda is to find a way for governments, insurance companies, and hospitals to pay for these very expensive treatments.

Pandemic preparedness

The versatility and agility of mRNA technology combined with the high level of coordination between industry and regulators enabled development, approval and distribution of the COVID-19 vaccine in record time. Looking forward, AMM is pursing development of a framework that will enable rapid deployment of mRNA vaccines for new pathogens as need arise.

Interpretation: More lobbying efforts are underway to integrate this technology into existing pandemic response technologies through the lobbying process, which involves giving money to Congress members.

Industry Website

I am often asked why there has been so much pressure to rapidly advance the authorization of mRNA drugs and vaccines. My standard answer is that the pharmaceutical industry sees this as a whole new unexplored area of pharmacology that can be exploited in developing and marketing new drug and vaccine products.

In other words, this is a gold rush.

When I first conceived the idea of using RNA as a drug in 1988, as the sole author, I initially published this concept in a small trade magazine called Focus after a patent disclosure in 1989. The article is linked here.

Focus: Using RNA as a Drug

Vical, was the company that I then worked for in the early 1990s, and this company was once featured in the CIA-associated magazine “Wired” with the breathless headline that it would be the next Microsoft – due to the DNA and RNA technologies that I had pioneered. Under the direction of my old boss Dr. Philip Felgner, Vical turned away from mRNA as a platform and focused on lipid-based plasmid DNA delivery, spent well over a billion investor dollars, completely failed to bring any significant products to market, and went bankrupt. Felgner eventually landed a plum academic position at the University of California, Irvine.

Just for the record, I have never received any inquiries from this industry concerning my experience, observations and conclusions concerning the technology platform that I launched with my inventions and invention disclosures in the late 1980s while working on my PhD at the Salk Institute (pre-Vical).

But now this new industry hopes that the old “Wired” prophecy will finally come true. The truth is that they really don’t care if it is “safe and effective” as long as they all make a killing on the increased stock valuations and/or IPOs generated from the new bio-opportunities. And if the tech doesn’t turn out so well, then “pump and dump” is always an option. Either way, the biotech investors win.

If you wish to better understand how industry insiders see the issues and prospects that they believe are opening up to them, I recommend the following article authored by AMM staff member Deborah Day Barbara, and review the other articles at the “Advancing RNA” website.

Trouble in Pharmaceutical Paradise

Getting back to the Nature magazine news feature article quoted at the start of this essay, and which you can read here, despite all of the rosy projections, the fledgling mRNA drug industry is facing unexpected challenges. And these are the direct consequence of Peter Marks’ “Operation Warp Speed” (with a strong boost by biodefense spook Bob Kadlec and the notorious Dr. Anthony Fauci), which jammed the technology through product development, manufacturing and testing by bypassing almost all applicable regulatory hurdles and directly into the arms of much of the worlds adults, adolescents, children, and pregnant women with profound disregard for the consequences.

You might say that “the industry” is now being hoisted with its own petard. Returning to the Nature article, what jumps out is that there is neither acknowledgement nor even entertainment of the idea that the industry has destroyed its own credibility out of greed and its own mis- and disinformation about the technology and its risks.

Five years ago, the US government was spending billions of dollars to support the development, manufacturing and roll-out of mRNA vaccines, which played a major part in curbing the COVID-19 pandemic. Pharmaceutical companies were pouring in capital and building ambitious pipelines centred on mRNA. The technology was feted with a Nobel prize. Investor confidence was sky-high.

Now, in the span of just a few months, the mood across the industry has grown darker — chilled by a newly hostile political climate.

One contract manufacturer of mRNA products has seen a substantial decline in business as government-backed vaccine programmes have their funding pulled, according to a senior company executive. Another biotech executive says that his mRNA-focused company is considering relocating planned clinical trials for anti-viral vaccines to outside the United States — or scrapping them entirely, shifting the firm’s focus to less politically volatile therapeutic areas. “It’s all just a commercial and regulatory risk now,” he says.

Both executives requested anonymity to avoid drawing political attention to their companies — but their experiences reflect a broad upheaval that is now rippling through the industry. In a survey released this month by the AMM, nearly half of 106 senior biotech and pharma executives reported direct impacts from US policy shifts this year — including project downsizing, budget cuts, delayed investments, terminated partnerships, job losses, hiring freezes, and planned relocation of operations overseas.

Even the term ‘mRNA’ has become a political lightning rod; its charged connotations now influence scientific discourse and health policy far beyond the vaccine debate. “That paranoia has gotten wrapped into mRNA as a word,” says Jeff Coller, an RNA biologist at Johns Hopkins University in Baltimore, Maryland, who is also involved in several small biotech firms.

Seeking to reframe the narrative, Coller and others are mobilizing around a strategic communications offensive, emphasizing mRNA’s potential not just in thwarting infectious threats but also in treating many of the same chronic conditions targeted by Kennedy’s ‘Make America Healthy Again’ initiative. The campaign to rehabilitate mRNA’s reputation starts at the top: with appeals to Trump’s legacy as a champion of medical innovation.

AMM leaders are preparing to publish a series of editorials that make the case that Trump’s decisive leadership during Operation Warp Speed — the 2020 programme that delivered COVID-19 vaccines in record time — marked the beginning of a new chapter in biotechnology and positioned the United States at the forefront of what many see as the fourth great wave of pharmaceutical innovation, after small-molecule drugs, biologics and cell and gene therapies.

Framing it as a chance for Trump to cement his place in medical history, they are urging the president to build on the foundation that he helped to lay. In particular, they pointed out that, by supporting mRNA-based cancer treatments, he could achieve a major unmet goal that was advanced by his predecessor Joe Biden, who had made “ending cancer as we know it” a signature priority. Trump “could be the president who is a true visionary on cancer”, says Coller, a leading academic voice at the AMM.

Such messaging just might resonate. Although Trump criticized the roll-out and mandates surrounding the COVID-19 vaccines in the period between his two terms, allies say he remains proud of the part he played in accelerating the technology’s development. “President Trump believes that Operation Warp Speed was a roaring success, and that the COVID mRNA vaccines were his great achievements,” says Robert Malone, a scientist involved in foundational mRNA research and a high-profile voice in conservative-leaning health-policy circles.

“But leading the charge against mRNA technology are individuals in the ‘medical freedom movement’ — Kennedy chief among them. They contend that COVID-19 vaccines were rushed through approval without adequate long-term testing, alleging that safety corners were cut in the name of speed, and that the risks of mRNA platforms continue to be deliberately downplayed.

At his confirmation hearing earlier this year, for example, Kennedy — who previously described an mRNA-based COVID-19 jab as the “deadliest vaccine ever made” — persisted in claiming that the vaccine was recommended for young children “without any scientific basis”, despite published clinical-trial evidence to the contrary.”

Public-health researchers and vaccine scientists emphasize that mRNA vaccines have consistently demonstrated robust safety and effectiveness in preventing severe COVID-19 outcomes, supported by extensive data from rigorous clinical trials and real-world studies. Yet, with trust in institutions and in the biomedical establishment crumbling, some argue that pulling back from mRNA is the only responsible course of action — not because the science is flawed, but because the damage to public confidence is too deep.

“If mRNA has a chance to have impact in the future, there needs to be a restoration of public trust around it,” says David Mansdoerfer, a political consultant in Fort Worth, Texas, and a former senior HHS official in the first Trump administration. To that end, he, like many associated with Kennedy, would support federal regulators withdrawing approval for all COVID-19 vaccines that initially entered the market under emergency-use provisions — including the mRNA-based ones that later won full approval. Mansdoerfer advocates re-evaluating the jabs under a standard review process.

The problem of mRNA’s reputation isn’t just a communications challenge — it’s a systemic liability. “I fear the brand is damaged for most uses,” wrote Vinay Prasad, a haematologist–oncologist at the University of California, San Francisco, in a Substack post in March. A vocal critic of COVID-19 vaccine mandates under Biden, Prasad was selected this month to lead the division of the US Food and Drug Administration that oversees vaccines and other biological products.

The branding issue for mRNA is not just a problem in the United States either. An analysis of social-media data across 44 countries, published last year, found “widespread negative sentiment and a global lack of confidence in the safety, effectiveness and trustworthiness of mRNA vaccines and therapeutics”

For anyone interested in 2023, The Malone Institute compiled a list of nearly 800 peer-reviewed papers on the adverse events associated with the mRNA Covid-19 vaccines. That list could now easily be tripled. So, Nature may choose to overlook the adverse events associated with this technology, but the rest of us know better.

Of course, the magazine “Nature” is fooling itself, and maybe fooling its readership, but it is not fooling the new Commissioner of the FDA, as we reported in a previous substack essay or any of us in MAHA.

Transcript of FDA Commissioner Dr. Makary:

“Look, I’d love to see the evidence to show that giving young, healthy children another Covid shot, you know, a sixth Covid booster, would help them. But that evidence does not exist. And so, we’re not just gonna rubber-stamp things at the FDA, and I don’t think you’re going to see a push at the CDC to be pushing Covid shots in young, healthy children.

That is something that’s being discussed right now.

I think you’re gonna see some announcement on that in the coming weeks, but I know they are trying to review all of the scientific data, and guess what? There’s no data. There are no good randomized control data that the current version, the latest formulation of the Covid shot is necessary for young, healthy children.

Other countries have already recommended against it. Other, leading countries in Europe have recommended against it for young, healthy children.

So, I think you’re gonna see this, and you’re gonna hear something forthcoming.”

FDA – Dr Makary on Real America’s Voice

Lately, we have heard a lot from the nattering nabobs of negativity within the MAHA base. Secretary Kennedy has betrayed them, they say. Marty Makary is not moving fast enough. On and on. The vaccine injured must be heard, acknowledged, and somehow made right- they shall not be denied!

But get real. Do people really think that Secretary Kennedy is going to abandon this issue because – well, why? “Because the pharmaceutical industry has co-opted him?” Not likely!

Then said Jesus unto him, Put up again thy sword into his place: for all they that take the sword shall perish with the sword.

Matthew 26:52

The mRNA medicines industry exists because the United States Government, and in particular DARPA, DTRA, NIAID, USAID, and, in particular, Dr. Anthony Fauci, willed it into existence.

Now the worm has turned, and the carelessness, hubris, disregard for established regulatory and bioethical norms, and general sense of entitlement of the industry and its supporters have backfired, and champions have risen to defend the population from these entitled academics and biopharmaceutical industry types. The politics have shifted, and those who abused public trust are now running for cover.

As well they should. And who is it that they are most afraid of?

  • HHS Secretary Robert F. Kennedy Junior.

Let that sink in for a moment.

And then, the next time you hear someone blathering on about how RFK jr. has betrayed them, gently invite them to relocate to Canada. Because he is on the front line, taking the heat, and 99.999% of those detractors are armchair quarterbacking, and the majority of those are hiding behind pseudonyms.

DC politics is a blood sport. Just ask the President. And patience is a virtue. I have faith in Secretary Kennedy and his team to get the job done. Maybe you could consider joining me in that?

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© 2025 Robert W Malone, MD
Virginia

 

Jun 272025
 

Recommend:    Go to   THIS PDF COPY.       2025-07 Lymphatics

The formatting and diagrams are intact.

I am having an awful time with the following copy.    /Sandra

– – – – – – – –

2025-04-19 Lymphatic System / Lymph Treatment

2025-04-19 Lymphatic System / Lymph Treatment

 

 

I answered “I had a lymph treatment just last week.”

The Dentist replied,  “What’s that?”

– – – – – – – – –

 

We have become divorced from KNOWING our amazing IMMUNE SYSTEMS.

I thought I’d start with some stories about the LYMPHATIC SYSTEM.    It should be interesting to go from there to the wider Immune System.  I will try to do that.    If I fail,  maybe it will spur you to clarify your thinking.    And in that way,  we’ll all learn something!

 

Try this:   

BODY HEALTH = LYMPHATIC SYSTEM  + CARDIOVASCULAR SYSTEM +  IMMUNE SYSTEM

The equation can be expanded and played with.

 

– – – – – – –  – – – – – – – – –

CONTENTS

  1.      THE COMPLETE HUMAN BODY    in pictures
  2.      LYMPH,  copied from the Index of COMPLETE HUMAN BODY provides an overview
  3.      RIGOR OF (LYMPHATIC + CARDIOVASCULAR + IMMUNE SYSTEM + SPIRITUAL)
  4.      EQUATIONS
  5.      IMMUNE SYSTEM,  DETOXIFICATION,  AND POISONING
  6.      AN EQUATION IS A TEETER-TOTTER         RELEASING THE INSULT BY SPEAKING IT
  7.      GETTING RID OF POISONS,  INTERNATIONAL COOPERATION
  8.      KEEPING THE POISONS,  INTERNATIONAL COOPERATION
  9.       INTELLIGENT DESIGN  IN THE HANDS OF THE  NOT-INTELLIGENT
  10.       THE LYMPH SYSTEM SAVED MY DAUGHTER’S LEG WHEN DRUGS COULD NOT

 

 

FOR MY DENTIST  – – THE LYMPH SYSTEM

 

  1. THE COMPLETE HUMAN BODY  in pictures

MY EXPERIENCE . . .The week after the lymph treatment  I was waiting for a friend in the chiropractor’s office.

 

A large book “The Complete Human Body, The Definitive Visual Guide” by Prof Alice Roberts caught my eye.   (She is a Prof,  an artist, and more.)   Wow!   This book could help explain THE LYMPH SYSTEM  to the dentist.

 

I ran to the bookstore and ordered “3RD EDITION,  ENHANCED AND UPDATED  $66.  (The definitive guide to the development, form, function, and disorders of the human body.)

 

 

This book – – which is a bit like a user’s manual – –

should be of interest to anyone young or old,

who inhabits a human body.”

 

It is a superb book for my purposes!

 

 

  1. LYMPH,  copied from the Index of COMPLETE HUMAN BODY  provides an overview :

INDEX,  P. 525    (The Complete Human Body,  3rd Edition)

 

lymph   366 -367

lymph nodes  75,76, 366, 367

and adaptive immunity  370, 371

blood vessels  77

lymphatic circulation  366

INSERT, Sandra:  p. 27 a diagram  re Circulating Blood shows & explains a contracting leg muscle forcing blood upward.  The same system is used by the lymphatic system  – – When a muscle contracts, it shortens and tenses, creating movement. Conversely, when a muscle relaxes, it returns to its original, longer state. . .  with a referral to p. 366-67,  an illustration of the network of vessels and ducts of the Lymphatic System . . .

lymphatic ducts  166, 167, 169, 366

lymphatic system  26

abdomen and pelvis   188-189

and adaptive immunity  370, 371

anatomy   74 – 77

in bone  46

head and neck  134 – 135

hip and thigh   272 – 277

in liver  381

physiology   366 – 367

shoulder and upper arm   226 – 227

spread of cancer   441

thorax    166 – 167

lymphatics   75, 77, 366

lymph0blasts   481

lymphocytes   75, 7

adaptive immunity   370 – 373

functions   367

generation of   367

lymphomas   481

lymphoid tissue   75, 77, 367

lymphomas     481

 

 

  1.    RIGOR OF (LYMPHATIC + CARDIOVASCULAR + IMMUNE SYSTEM + SPIRITUAL)

 

I figure, EQUATIONS can be used to help explain  The Nature of Health.  . . .   How so?

 

  1. EQUATIONS

 

EQUATION  –  EQUATES TO  –  THE SAME AS  – –  THERE IS BALANCE

 

 

(Picture of a balance scale)

 

 

 

 

 

 

 

 

Add to one side of an equation or a scale and it becomes out-of-balance.

Add the same amount (a compensating amount) to the OTHER side and it’s back-in-balance.

 

     A TEETER-TOTTER IS LIKE AN EQUATION or a SCALE

  • It is  Level if the weight on both sides is the same
  • It is Upended if either side is overloaded

 

Equations can be expanded.  You can play with them.   Learn from them.

 

 

(Pic of Equilibrium)

 

Call this THE GROUND LEVEL EQUATION:

 

BODY HEALTH                        =  LYMPHATIC + CARDIOVASCULAR + THE IMMUNE SYSTEM

 

If STRESSORS ARE IN BALANCE  with BODY HEALTH    =   PAIN  DOES NOT HAVE DOMINION

  • But ADD, or ADD MORE of  (stressor X,  Y,   Z)    – – –  cont next page

 

  • If you do that, you have to COUNTER-BALANCE by adding the same to the health side.

You come back into an equilibrium.

 

NOTE:  this does not apply to a pain that is PHYSICAL, e.g. a broken leg.

 

The medical model tends to be linear.  If you have a pain, the pain has a cause.  Treat the cause.  The medical model may work just fine for the broken leg.

 

The theory (I believe it and don’t change the belief until something happens to show that the belief is wrong).  The pain theory I am working on (for a long time) includes:

 

You do not have to remove ALL exposures to one allergen  (I use the word “STRESSOR”.)    The GOAL is to REDUCE THE OVERALL LOAD of stressors.  The IMMUNE SYSTEM will recuperate, given time and support.   (As long as you haven’t progressed past a tipping point.)

 

(NEED:   a discussion of STRESSORS.)

 

(Pic teeter-totter PAIN)

 

 

It’s easy to understand that

Loading too many kids on one end of the teeter

Throws the other end up into the air.

 

If there’s PAIN, it is pushed up

When Stressors are loaded up.

No mystery in that

You have to un-load.   It does not matter

Whether a whole lot of one Stressor is removed, or

Smaller amounts of a number of Stressors.

 

 

 

Release the opportunity for Pain by speaking it,  ASAP

Before it has time

To create a rut

In your mind

Neural plasticity/pain re-processing (Applied)!

 

RECOMMMEND:  Practice  SELF-ADVOCACY lots, first!

 

STRESSORS,  RELATIONSHP TO SELF-ADVOCACY

To Be Written

 

  • NOTE re MIND-BODY:   Not all PAIN is LINEAR in relation to CAUSE.  Think, for example, of pain related to early childhood.   Also,  PAIN moves around in the body and takes different (interchangeable) forms.

 

Your Body is not stupid nor is it gullible.   It is up to you to COMMIT to it.    After years of ignorance, neglect and abuse by You and your Society,  it is not easy to get back to Health.

 

Your Body knows what’s going on.  It is very worth your while to learn to Work with it!  The more You  (CONSCIOUS and VERBAL) learn how to communicate with your Body  (SUB-CONSCIOUS and NON-VERBAL), the greater becomes your ability to figure out what your body is teaching you.    This is the realm of the Spiritual aspect of your Being.

 

The Medical System is very good at telling you something is the cause.  However, it is not always well-informed or honest.   Case in point, from our recent work:    The Simpsonwood Story      https://sandrafinley.ca/blog/?p=31658

 

The biggest problem is that the model chosen for the Medical System is a  COMMERCIAL  model, which is NOT APPROPRIATE for The FUNCTION  we EXPECT it to perform for us.

 

There’s money to be made by producing PRODUCTS THAT BREACH BARRIER MECHANISMS OF OUR IMMUNE SYSTEMS.

 

Both Business and Government revenues increase.

 

Which means there is NO  ONE EXCEPT YOU , THE INDIVIDUAL to rise against foes who are thrusting spears through the BARRIERS that have evolved over millennia to keep our brains and our babies safe.

 

It’s the truth.   You might as well accept it.

I can agree to capitulate – –  to not see it.  However,  that would be a short-term fix, and it would be a monumental betrayal.

The betrayal can be understood in the framework of “The Tragedy of the Commons”.

 

(The internet – – the air waves – – are part of “The Commons”.)

EXCERPT FROM  Battles to protect the Commons.    https://sandrafinley.ca/blog/?page_id=9

. . .   battle-fronts to protect The Commons in an era of unprecedented assault on them.   Our success or failure affects the ability of future generations to care for themselves.

When there are incursions onto the Commons, people have to come together to defend it.  If not, the Commons is lost and the whole community suffers  – – a lot.

OTHER people work hard, all the time, in defence of the Commons.  Without them, one tiny example,  the quality of the water coming out of your tap would be less than it is.   Many more people would side-step the issue through the purchase of bottled water, if they can afford it.

There have been monumental efforts by people in Canada and the U.S. to stop things like tiered (preferential) access to the Internet that large corporate interests seek.

One woman, Brierley Newton, stood in defence of the Commons.  She is not asking us for our gratitude.  But she should expect that we will at least stand in solidarity when the ball lands in our court.

You might think of the case of Amanda Todd (a teen who committed suicide as a consequence of on-line predation.

If I capitulate (keep my mouth shut), not only is a grotesque belief reinforced, but the perpetrators make unbelievable money.  These are Global forces, they win, which only empowers them to do more.

We leave a more violent world behind us, if we do not accept our responsibility.

We stand by while ignorant people continue to kill us by thrusting more and more spears through parts of us that keep us alive and thriving.  (e.g.  Barrier mechanisms in our Immune Systems)

The tragedy and comedy of human existence:   we are often unwitting participants in our own death and destruction.

 

 

 

 

 

 

 

The good news is?   The world is changing.

2019-03-13 The Ombudsman will fail. They have a problem with “Trust” but fail to identify that the problems are INHERENT in the system. “Extractive Sector Corporate Responsibility“.   SNC Lavalin,  Jane Jacobs.

https://sandrafinley.ca/blog/?p=24156

 

I say  INHERENT.  I shout    INHERENT.  

They are uneducated.   They do not know what that word means,         INHERENT    INHERENT

 

  1. 5.     IMMUNE SYSTEM, DETOXIFICATION, AND POISONING

 

HEALTH  =  LYMPHATIC + CARDIOVASCULAR + THE IMMUNE SYSTEM  + SPIRITUAL (PURPOSE) HEALTH  =     LYMPH  +             BLOOD    +  The IMMUNE SYSTEM =  DETOX (LIVER) + INNATE IMMUNITY           + ADAPTIVE IMMUNITY

 

INNATE IMMUNITY includes  BARRIER IMMUNITY  which you know as, for example, the blood-brain barrier, the placental barrier, . . .

If a Barrier Immunity is breached (very serious for your health),  and you try to pass it off as the fault of someone else,  you can forget about having a relationship with your Body. 

Your Body will not trust you to keep You and It safe.   Sounds crazy.  Well yes,  I am!  Ha ha!

– – – – – – – – –

I am not a doctor.   But I do know how badly-corrupted some medical and other systems are.   Ignoring the problems isn’t an answer.

I can make the following contributions to help us find solutions.

 

BE CLEAR.  I am NOT saying that if you

  • look after your LYMPHATICS + CARDIOVASCULAR +  SPIRITUAL (PURPOSE),
  • AND don’t overload your IMMUNE SYSTEM,  you will be healthy and without pain.

Human lords view us as ignorant and disposable:

2011-02-01      Aluminum and Vaccine Ingredients: What Do We Know? What Don’t We Know?      (https://sandrafinley.ca/blog/?p=1227)

 

2020-06-10    If I am making a choice about a vaccine, I want to know this.      (https://sandrafinley.ca/blog/?p=25074)

 

For more info on mercury, go to  “HEALTH” in the right-hand sidebar of my blog ;  scroll down to         Mercury poisoning, dental amalgams. See also Vaccinations.

 

#5  Continuing      IMMUNE SYSTEM,  DETOXIFICATION,  AND POISONING . . .

 

DETOXIFICATION   (liver)    (see HUMAN BODY  p. 381,  bottom left).     Words can make a topic look complicated.  Keep calm.  You already know much/most/all of it – – English is famous for having many different ways to say the same thing.   It helps keep people off-balance.

 

The IMMUNE SYSTEM   is   INNATE IMMUNITY +  THE ADAPTIVE IMMUNE SYSTEM

        •    I think of auto-immune diseases in terms of  INNATE and ADAPTIVE IMMUNITIES  that have been completely overpowered.

 

On p.134  there’s a picture of a skull (head and neck)  with the lymphatic system in green.    What I see is the OPENINGS – – eye sockets, nasal cavity,  and mouth/teeth.

If you know lymph, and

 

 

 

 

 

would you call it a  “DESIGN FLAW BY HUMANS” to put poisons  (mercury, aluminum, and other)  in the eyes, nasal cavity,  and mouth/teeth?   How about if it’s your baby?

 

Eyedrops, various kinds, that contain mercury and                                                  other goodies go into eyes                                       MORE STRESSORS

 

I do not know what’s in nasal sprays.                     MORE STRESSORS

 

Mercury started going into mouths in the first part of the 1800’s.   See  A Brief History.

https://www.toothbythelake.net/wellness-center/amalgam-fillings/a-brief-history-of-amalgams/#:~:text=1819:%20A%20Mercury%2Dbased%20dental,use%20of%20mercury%20amalgam%20filling.

 

And then there’s vaccines by injection.    We are certifiably daft.

 

Hmmm – – “encapsulation” would be a mechaniusm of the Immune System.  If we knew just a little bit about it,  that would be helpful in making decisions when you encounter it.

 

 

There are problems with commercial (purchased) science that make me close my eyes.  We treat more mercury and more aluminum and more glyphosate and more mRNA and more chemicals and more toxic chemicals as “Business as Usual“.    Business (Money)  is a priority to us.  MORE THAN health. And more than species survival ??

 

In 2003 Canada caught up with long-known European research:  FINALLY scientists from the National Water Research Institute (NWRI) published research about the “feminization of fish downstream from water treatment plants” (that’s what sewage treatment plants are called).

 

Finally we were talking about what’s going into our Waterways, and the implications.  The “feminization” of fish was associated with all the women on birth control pills flushing pee down the toilets into sewage that emptied into waterways.  Something more happened.  More men are gay (feminized) – –  a higher percentage.  I believe that is an established fact.

 

I have long wondered whether changing sexual and gender information might come from more and more ENDOCRINE DISRUPTORS, hormone disruptors.  There are thankfully, good debates about that on the internet.  It seems to me that if the agricultural industry continues to use increasing amounts of endocrine-disrupting chemicals and has been using them since the 1950s, this forever more will have repercussions.  Vietnam veterans were exposed to a TCDD-contaminated military herbicide (Agent Orange).

Agent Orange exposure increases morbidity from endocrine and neurologic diseases.

 

Credentialed people are credentialed, not more than that.   The good news is the crack in the dam.   People love to learn and they love to talk with each other.

 

If you happen to read Suzanne Humphries’ book, “Dissolving Illusions”  the word “lymph” is used in printed material from the 1800’s, without need for defining what it is.

 

The HUMAN BODY (P. 370-71)   “The adaptive immune system provides the body with the means to develop highly specific immune responses to particular pathogens encountered during its  life span.  Crucially, such responses may be quickly redeployed if a pathogen infects.”   

 

  1. 368-9   Lymphatic Circulation

I think my Lymphatic Circulatory system is fairly intact.  But I wonder what happens when lymph networks in the Body are severed?   (for example when joint replacements are implanted?)

 

If we made it our business to help teach a whole lot of Canadians about our Immune Systems,       

The Ostrich Farmers, and the Ostriches

Health Canada,  the CFIA,   Teresa Tam,  Bonnie Henry,  and a whole lot of others – –

Canadians MIGHT not

have time to destroy our Immune Systems before they’ve had time to even learn about them?

 

They tell us that their products are better, superior to our Immune Systems.  Well I suppose they are right:  but it was not always so.

 

Good grief!   Their assault on us is an assault on the inside of our Bodies!

 

 

MY LIFE EXPERIENCE WITH BREACHES OF BARRIER IMMUNITY 

(My Mother kept very good records.)

 

Neuro Toxins like mercury by-pass the blood-brain barrier, the placental barrier . . .  They SLOWLY poison.

 

    1.   Mercury fillings (dental amalgams starting with fillings in baby teeth (no comment!) and continuing into adulthood).
    2.   Vaccines – – mercury by injection.  (The preservative thimerasol in vaccines, started in early childhood)
    3.   Mercury in wetting and soaking solutions for contact lens, starting in high school (1967).
    4.   Joe Bourgault experience.  Grant Schoenroth also.  Mercury poisoning from dental amalgam.   The Medical profession could not diagnose it.  Both men thought they were going to die.  Removal of mercury amalgams and slow de-tox restored their health.
    5. IAOMT  (International Academy of Oral Medicinet and Toxicology) .  Dave Warwick’s experience as a new young dentist in his home-town of Hanna, AB took him into mercury-free dentistry.  Decades later,  Dave agreed to do the “Mercury Jamboree” at the University of Saskatchewan. I personally sent an individual invitation to almost everyone at the University in Dentistry, in Toxicology, in Water  – –  ONE employee came anonymously.

 

I organized it;  Joe Bourgault and Grant Schoenroth both told their experiences, Dave spent the day with everyone who came,  doing demonstrations, taking readings, answering questions, making recommendations.

 

My family members and I have had mercury removed  by a dentist who has been trained on handling the mercury.

 

MANY people suffer from mercury poisoning.  I think of Grassy Narrows, Ontario.   (https://www.thecanadianencyclopedia.ca/en/article/grassy-narrows).  There are lots of people like Joe and Grant.   I suspect it is more usual that people die without ever knowing that it was mercury poisoning that got them.  The most likely way of discovering the poisoning is if you have a friend who tells you about it.

 

Safe removal of the mercury fillings is a life-saver for some people.  Mercury (“dental amalgam” a.k.a. “silver fillings”) should not be installed in teeth.  Dental colleges are complicit.  Mercury fillings are cheaper,  BUT ONLY in the short run.   The public purse pays for the longterm costs (cognitive and other disabilities and illnesses or premature death).

 

Slow accumulation and poisoning coincides with aging.  The wrong diagnosis is easily assigned.  The same as the wrong diagnosis was assigned to me when I was 3 years old.   Within a couple months of each other I had dental amalgams (silver mercury fillings) put in my teeth and vaccine with mercury in it by injection.

 

My legs started aching.   This was the early 50’s in Canada.    Mom took me to the local doctor who referred us to the “City Doctor”, a 3- hour drive away.  Surprise!  The diagnosis was polio.

 

A few years ago I asked  “Who else in this area had polio?”    My Mother replied,  ” Well, that was the funny thing:   NO ONE.”   Mercury poisoning was diagnosed as polio, I have no doubt.

 

= = = = = = = = = = = =

 

  1. GETTING RID OF POISONS,  INTERNATIONAL COOPERATION, MERCURY,  THE MINIMATA CONVENTION

 

The Minamata Convention on Mercury is a UN treaty aimed at reducing mercury’s impact on human health and the environment. It addresses the entire lifecycle of mercury, including its supply, trade, use, emissions, and disposal. The convention seeks to phase out mercury-added products, control emissions from various industries, and promote international cooperation on mercury management.

 

Here’s a more detailed look at the key aspects of the Minamata Convention:

Key Provisions:

  • Phasing out mercury-added products:

The convention includes provisions to phase out or restrict the use of mercury in products like batteries, switches, lamps, and cosmetics.

  • Controlling emissions:

It aims to reduce mercury emissions from key industries such as coal combustion, waste incineration, and cement production.   (INSERT. Sandra – – someplace on my blog there’s the report on a jurisdiction where it costs more to get cremated if you’ve got dental amalgams because of the mercury going up the smokestack!)

  • Managing mercury trade:

The convention regulates the export and import of mercury and mercury-containing products.

  • Addressing artisanal and small-scale gold mining:

This sector is a major source of mercury pollution, and the convention includes measures to reduce mercury use in this area.

  • Safe storage and disposal:

The convention addresses the safe storage and disposal of mercury waste.

International cooperation:

It promotes international cooperation on mercury monitoring, research, and the development of safer alternatives.

Historical Context:

  • The convention is named after Minamata Bay in Japan, where widespread mercury poisoning occurred in the mid-20th century.
  • The experience with Minamata disease highlighted the devastating effects of mercury pollution and the need for global action.

Current Status:

  • The Minamata Convention entered into force in 2017.
  • As of [June 2025], the convention has been ratified by 150 states.

 

(INSERT, Sandra:    Canada signed the Minimata Convention on October 10, 2013, and ratified it in April 2017, with the treaty entering into force in Canada on August 16, 2017.   

 

You can’t put mercury down the drain into water supplies.  Dental offices are supposed to capture waste that has mercury content and dispose of it as a hazardous waste.  Has the regulation ever been enforced?   Do we protect the workers in dental offices by stopping the use of dental amalgam (“silver fillings”) .

 

What does the Cdn Dental Association have to say?  https://www.cda-adc.ca/en/about/position_statements/amalgam/      . . . Oh yeah . . .  the “safe” story,  BUT! Dentists have a responsibility!    And we still have . . .   COPIED FROM THE CDA website:

 

Current scientific evidence supports the use of dental amalgam as an effective and safe restorative filling material that provides a long-lasting solution for a broad range of clinical situations. Dental amalgam delivers significant benefits compared to other filling materials with respect to ease of use and longevity, especially in patients with a high risk of tooth decay.

The potential environmental impact of the mercury content found in dental amalgam can be managed through the implementation of best management practices, such as those outlined in the Memorandum of Understanding respecting the implementation of the Canada-Wide Standard on Mercury for Dental Amalgam Waste, signed by Environment Canada and the Canadian Dental Association in 2002. The Minamata Convention is a global treaty designed to protect human health and the environment from the adverse effects of mercury. Ratified by Canada in 2017, the Minamata Convention seeks to eliminate environmental risks by phasing down the use of dental amalgam worldwide.

 

Replacing functional or serviceable dental amalgam fillings (restorations) is unnecessary and ill-advised for reasons related to safety concerns or perceived health needs. A conservative approach to filling replacement, combined with effective decay prevention, is strongly advised to help maintain the dentition over a lifetime.

 

Dentists have a responsibility to ensure that any recommended treatment reflects the ethical and quality-of-care standards of the profession and that informed patient consent has been obtained. Specific clinical circumstances and facts should be discussed by dentists and their patients or decision makers (i.e., parents or guardians for dependents), so that the most appropriate filling material for a particular clinical situation is selected. Patients who request replacement of serviceable restorations need to be provided with sufficient information to understand the implications of this request.

 

CDA Board of Directors
Approved: February 2005
Revised: February 2021

 

Stop the make-believe.   As with  covid “safe and effective”,  in Canada.

 

Announcements are made to pacify the  electorate.  They go back to sleep.   The next time there is awareness, they  ask,  “I thought that was stopped.”  Use the example of mercury in the flu shot.  Or there are other examples to choose from.

 

 

  • Toxins DO bio-accumulate.
  • They DO  have synergistic effects when mixed.  And we know?   We could try UN-blocking the research that is needed, for example on water. (for pesticide residue – you might think it’s a no-brainer?  Chemical use on the land has done nothing but increase in aid of GMO crops that you can spray and not kill.  (Are the plants healthy??)(for radioactive residue)(for heavy metal pollution – – thinking of Halifax Harbour from the industrial process known  as electroplating)(for poisons – – remember the vaporooter debacle?)  Is the water poisoned?  Can you test – – you have to know the chemicals to test for, before you can test.

 

2025-06-26 CDC Vaccine Advisers Vote to Stop Recommending Flu Shots That Contain Thimerosal (Mercury)

2025-06-26 CDC Vaccine Advisers Vote to Stop Recommending Flu Shots That Contain Thimerosal (Mercury)

  • Parties are working to implement the convention’s provisions and achieve its goals.
    Dave Warwick is older than me.  He began practicing mercury-free dentistry early in his dental career after the experience and advice of patients.  He is a member of an association (the IAOMT)  whose members promote mercury-free dentistry.   Dave attended  UN International Negotiations  (“COP” – CONFERENCES OF THE PARTIES)  that achieved the Minimata Convention.Dave Warwick is a holistic, mercury free (amalgam-silver filling free) and mercury safe dentist and he is dedicated to practicing safe and healthy dentistry.    Dave’s been doing it for ? 3 decades now ?.    I would say that the CDA does not want to do healthy dentistry.  And the Govt of Canada is not genuinely concerned about your health.  Nor about the poisons we ingest.   That is up to us.   Share information with young people, especially.  It is comfortable old farts who stand in the way of change.In essence, the Minamata Convention represents a global effort to tackle the pervasive problem of mercury pollution to protect human health and the environment from its harmful effects.   (But it’s okay to use it in dental amalgams (“Silver fillings”) and still in some vaccinations.  It is well documented on my blog.)

 

 

  1. KEEPING THE POISONS,  INTERNATIONAL COOPERATION

 

I don’t need to say more than The Covid experience is yet another example of BIG MONEY having its way.

 

It is  an issue of  CORRUPTION OF GOVERNANCE.   

 

See  – – 2022-02-28 Covid protests, Vocabulary and Context. WE WILL DO BETTER . . .  NEXT TIME! say the Police. Linguistics.

 

 

  1. 8. NEURAL PLASTICITY (This is,  I think, the route by which I can make the spiritual element more apparent.  I have trouble finding time to write it down.)   To be done.

 

 

  1. INTELLIGENT DESIGN  IN THE HANDS OF NOT-INTELLIGENT  is a Recipe for Disaster.   “The Government” currently in Canada, the Coup d’etaters).   See – –

 

2022-02-28 Covid protests, Vocabulary and Context. WE WILL DO BETTER . . .  NEXT TIME! say the Police. Linguistics.

 

  1. THE LYMPH SYSTEM SAVED MY DAUGHTER’S LEG WHEN DRUGS COULD NOT

 

I WANT to contribute to the upgrading of what we know about IMMUNE SYSTEMS.   What we know is woefully inadequate.   It makes us VULNERABLE to manipulation by the medical system.

 

 

CONFESSION,  MY ATTITUDE:  If your  child’s Barrier Immunity is breached, it’s your responsibility.  WHY?

Because if there’s money to be made by producing products that breach IMMUNE SYSTEMS  (- – these are immune systems that have developed over millennia to keep us SAFE)

 

  1. Both business and Government benefit from more money.

2,   Which means WE HAVE LOST the “Guardianship” Role in our societies.

  1. There IS no one, EXCEPT YOU, to defend your Self and your offspring.
  2. A LITTLE bit of help from MILLIONS of people is a lot.
  3. If I’m wrong, please share what you know that I don’t know.  Thanks.
Jun 262025
 

 NOTE:  a concoction with “M-E-R” in the name has some form of MERCURY  in it (thiMERasol).

– – – – – – –

The Advisory Committee on Immunization Practices, or ACIP, voted separately on thimerosal-containing flu shots for children, pregnant women and adults. All three recommendations passed with a 5-1 vote and one abstention. Thimerosal was removed from all routine childhood vaccines in 2001, but is still used in some flu shots, including those given to children and pregnant women.

flu vaccine and word "thimerosal"
Download     00:00/10:18

In a series of votes today, the CDC’s new vaccine advisory committee voted to no longer recommend flu vaccines that contain thimerosal, a mercury-based preservative linked to neurodevelopmental disorders.

The votes, part of a two-day meeting of the Advisory Committee on Immunization Practices (ACIP) that concluded today, took place after a presentation on the health risks of thimerosal by Lyn Redwood, a nurse practitioner with experience in pediatrics and family medicine.

Redwood, president emerita of Children’s Health Defense (CHD), presented as a private citizen. However, she will soon join the Centers for Disease Control and Prevention (CDC) in its vaccine safety office, multiple officials told CBS News.

Thimerosal is a preservative used in multidose vaccine vials to prevent the buildup of bacteria and fungi. It was removed from all routine childhood vaccines in 2001.

BEWARE – – manipulation of data

(INSERT, Sandra:  The vaccine pictured above is “multi-dose”.   (There are 10 doses in the bottle.)  See 7 paragraphs below  “Hooker said thimerosal “is still used in multidose vials of the flu shot, which have in the past comprised nearly half of all the flu shots given in the U.S., including those to pregnant women and infants down to age 6 months.”

Also note:  2025-03-02 COVID VACCINE LOTS IN CANADA  (B.C.) identified as source of Adverse Events Following Immunization (AEFI)

During her presentation, Redwood warned that mercury exposure “is a cumulative issue,” as the substance builds up in the body over time, including through repeated vaccination with shots containing the substance. She said it is “very feasible” to use alternative preservatives in single-dose vials.

ACIP voted separately on thimerosal-containing flu shots for children, pregnant women and adults. All three passed with a 5-1 vote and one abstention. The abstaining member, Vicky Pebsworth, Ph.D., a registered nurse, cited the vote’s wording, which did not make a distinction between recommending flu vaccines in general and recommending against multidose vials.

Dr. H. Cody Meissner, professor of pediatrics at Dartmouth’s Geisel School of Medicine, was the lone committee member to vote “no” for each of the three motions. “No study has ever indicated any harm from thimerosal,” he said.

In a separate vote, ACIP unanimously reaffirmed its recommendation for annual flu shots for all people 6 months and older who do not have contraindications.

In a statement following today’s votes, ACIP said, “We came to this meeting with no pre-determined ideas and will make judgements as if we are treating our own families. Unbiased scientific thinking is fundamental to the committee’s charge.”

Brian Hooker, Ph.D., chief scientific officer for CHD, called today’s outcome “a huge first step towards limiting toxic exposures especially to our most vulnerable individuals.”

Hooker said thimerosal “is still used in multidose vials of the flu shot, which have in the past comprised nearly half of all the flu shots given in the U.S., including those to pregnant women and infants down to age 6 months.”

According to CNN, most flu vaccines given in the U.S. come in single-dose vials that do not contain thimerosal, but around 4% come in multidose vials that do contain the preservative. Redwood cited data indicating that during the 2019-2020 flu season, over 60,000 pregnant women were vaccinated with multidose vials.

Today’s vote ‘20-plus years in the making’ — but concerns remain

Dr. Meryl Nass, who live-blogged today’s meeting for CHD.TV, wrote that the votes can be interpreted as a “yes for everyone getting a [flu] shot.”

Beth Clay, executive director of the International Chiropractors Association and a former congressional senior staffer who led the last comprehensive inquiry into issues related to vaccine injury, applauded ACIP’s vote, saying, “It’s 20-plus years in the making.”

However, she expressed concerns about the wording of today’s motions.

“I appreciate the clarification and education Pebsworth provided about the verbiage of the motions,” Clay said, suggesting that a vote on recommending an annual flu vaccine should have been held separately from a vote on the recommendation that flu vaccines offered to the public should be thimerosal-free.

“How you ask a question matters,” Clay said.

ACIP makes vaccine-related recommendations to the CDC director, who has the discretion to accept or reject them.

Until March, the agency’s acting director was Susan Monarez, Ph.D. She stepped down that month after President Donald Trump nominated her for the permanent director’s position.

Last month, U.S. Health and Human Services Secretary Robert F. Kennedy Jr. reported that attorney Matthew Buzzelli is currently acting director, while Monarez awaits U.S. Senate confirmation hearings.

Clay said that following today’s ACIP vote, the CDC may require the Vaccines for Children Program, a taxpayer-funded program providing vaccines to underprivileged children, to remove multidose flu vaccines and allow only the single-dose shots that don’t contain thimerosal. She suggested that today’s votes should have clarified that.

Thimerosal levels in flu vaccines 250 times higher than EPA safety limit

In the days leading up to this week’s ACIP meeting, several media outlets and medical organizations criticized Kennedy’s decision to dismiss the committee’s 17 former members earlier this month and appoint eight new members in their place.

Earlier this week, Sen. Bill Cassidy (R-La.), chair of the U.S. Senate’s Committee on Health, Education, Labor and Pensions, called for the postponement of this week’s ACIP meeting, citing concerns that its new members are biased against vaccines.

After the final agenda for this week’s ACIP meeting was published earlier in the week, media criticism turned to the inclusion of Redwood’s presentation on thimerosal, with CNN reporting that experts “found the inclusion of the topic on the ACIP agenda puzzling.”

The Guardian cited Dr. Paul Offit, director of the Vaccine Education Center and an attending physician in the Division of Infectious Diseases at Children’s Hospital of Philadelphia, who suggested there was no point in discussing thimerosal.

In a post on X Tuesday, Kennedy responded to a report by The Guardian last week characterizing thimerosal as safe, noting that thimerosal’s label advises against its use during pregnancy, and that thimerosal has “never been shown to be safe.”

Redwood’s presentation noted that thimerosal was first used as a vaccine preservative in the 1930s without any studies demonstrating its safety. The U.S. Food and Drug Administration (FDA) later “grandfathered” thimerosal as an approved vaccine ingredient without performing adequate safety testing.

Redwood said thimerosal has a 49.6% concentration of mercury — the third most toxic element for humans — and that thimerosal levels in flu vaccines are 250 times higher than the U.S. Environmental Protection Agency’s (EPA) safety limit.

“Thimerosal can cross the placenta and blood-brain barriers and converts to inorganic mercury in the brain,” Redwood said, noting that infants, young children, older adults, pregnant women and fetuses are particularly vulnerable to its effects.

Redwood, RFK Jr. push back at media claims that thimerosal is proven safe

Redwood’s presentation — and Kennedy’s X post — also addressed the mainstream media’s narratives by citing several studies that have demonstrated thimerosal’s risks to human health.

This included a 2001 Institute of Medicine report finding that the link between thimerosal and the rise of neurological conditions in children, including autism, is “biologically plausible.” The report recommended the termination of all vaccines containing thimerosal.

Redwood cited a 2005 primate study funded by the National Institutes of Health, which found that ethyl mercury — the type of mercury in thimerosal — more rapidly converted to inorganic mercury in the brain, resulting in increasing concentrations of inorganic mercury and subsequent neuroinflammation.

Redwood also cited a 2014 study finding that the half-life — the time needed for the concentration of a substance to be reduced in half — of inorganic mercury in the human brain ranges from five to 27 years. A 2016 study suggested there “may never be a safe level of mercury exposure, especially for an unborn child.”

Redwood also noted evidence contradicting claims that thimerosal is effective as a vaccine preservative and disinfectant. She cited a 2004 incident at a Fluvirin vaccine manufacturing plant, which was forced to close after it became contaminated with Serratia marcescens, a bacterium, even though the Fluvirin vaccine contained thimerosal.

According to Redwood, peer-reviewed studies published as far back as 1948 questioned the safety of thimerosal.

Kennedy suggested that The Guardian “did not bother to cite any peer-reviewed study” to support its claim that thimerosal is safe. Instead, The Guardian relied on “a fact check website operated by the Pharma-funded American Academy of Pediatrics” that “likewise cites no peer-reviewed study to support this claim or its equally terse assertion that ‘Thimerosal has been removed from all routine childhood vaccines.’”

In 2014, Kennedy authored “Thimerosal: Let the Science Speak,” in which he argued that there is a “broad consensus among research scientists that thimerosal is a dangerous neurotoxin.”

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Thimerosal is cost-effective for vaccine manufacturers

Hooker agreed with Redwood and Kennedy’s conclusions. “Thimerosal is mercury, and mercury is, straight-up, a neurotoxin. This has been shown historically in thousands of publications.”

In 1998, growing concerns over thimerosal’s safety led the FDA to determine that thimerosal is “not generally recognized as safe and effective.” In 1990, California recognized thimerosal as a chemical known to cause cancer, birth defects or reproductive harm, under a state law known as Proposition 65.

According to Hooker, pharmaceutical companies continue to use thimerosal because it is cost-effective for them. He said:

“Thimerosal enables flu shot manufacturers to continue to manufacture multi-dose vials, which are cheaper per dose. It also has been used to quell the furor of countries overseas where many vaccines on the infant/child schedule still contain thimerosal.

“This is especially true in developing nations. They use the U.S. as an excuse for these companies to continue to peddle cheap and harmful vaccines overseas.”

Hooker called on public health agencies to enact “a complete ban of the use of thimerosal as a preservative for the manufacture and formulation of vaccines.”

Related articles in The Defender

Jun 242025
 

Vaccine makers, pharmacists, professional medical societies and others opposed to recent changes in vaccine policy are banding together to create their own system for recommending and purchasing vaccines in a move designed to bypass government health agencies’ recommendations, The Washington Post reported.

washington post logo on cellphone and vaccines on a chess board
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Vaccine makers, pharmacists, professional medical societies and others opposed to recent changes in vaccine policy are banding together to create their own system for recommending and purchasing vaccines in a move designed to bypass government health agencies’ recommendations, The Washington Post reported.

Members of the new group, all of whom profit from the vaccine industry, along with some state health officials and a “new advocacy group,” are strategizing ways to preserve the vaccine status quo under U.S. Health and Human Services (HHS) Secretary Robert F. Kennedy Jr.

The anonymous group, which hopes to create “a nongovernmental vaccine system” for vaccine recommendations and purchasing, according to the Post, is engaged in a series of discussions.

Topics include ordering vaccines directly from manufacturers and prioritizing recommendations from medical associations rather than from the Advisory Committee on Immunization Practices (ACIP), which makes vaccine recommendations to the Centers for Disease Control and Prevention (CDC).

The move comes as Kennedy dismissed all of ACIP’s sitting committee members earlier this month due to concerns over conflicts of interest in the committee. He filled eight of the 17 committee seats a few days later.

Commenting on industry insiders’ efforts to create a new commission, research scientist James Lyons-Weiler, Ph.D., told The Defender:

“They want to create and lend authority to a corporation-backed, corporation-friendly committee to replace the one that was just disbanded. These moves would represent replacing the facade of regulating vaccines by a government agency with overt industry self-governance and regulation.”

The Post called the move by the unspecified group of actors “extraordinary,” but conceded that it “faces major challenges.”

For example, insurance companies typically don’t cover shots that aren’t recommended by ACIP. An ACIP recommendation is also the basis on which the federal Vaccines for Children Program pays for vaccines for minors whose families can’t afford them. That program covers vaccine costs for about half of U.S. children.

Also, in many states, pharmacists’ ability to prescribe or administer vaccines is tied to the adult and child immunization schedules recommended by ACIP. And state laws for school vaccine requirements, as well as requirements for healthcare workers, are typically tied to ACIP recommendations.

Another problem, according to the Post, is that “potential competing recommendations could sow confusion among doctors as well as patients if it becomes unclear which recommendations to follow.”

Lyons-Weiler said physicians should be wary of any recommendations coming from the nongovernmental group, especially because participating in federal programs while failing to comply with ACIP regulations could violate statutes.

“The dismissed ACIP committee members can form whatever opinion group they want, but physicians follow their recommendations over the rules and regulations of the HHS at their own peril,” he said.

In a recent article, Lyons-Weiler said calls to ignore recommendations from the new ACIP committee are largely circulated by the former ACIP members who were dismissed because of their ties to Big Pharma.

Former Merck consultant and dismissed ACIP member Dr. Helen Chu was quoted in a recent op-ed in MedPage Today as calling on physicians to “turn away” from ACIP’s vaccine recommendations. She received thousands of dollars from Merck in the year before her ACIP appointment.

Merck is the manufacturer of multiple major childhood vaccines, including the Gardasil HPV vaccine; the MMRII for measles, mumps and rubella; a chicken pox vaccine and several others.

“Undermining ACIP in favor of non-statutory organizations may represent a breach of federal compliance by physicians and healthcare institutions receiving federal funds,” Lyons-Weiler wrote. Chu should be well aware of that fact, he added.

Initiative pushes Pharma-linked medical associations to make recommendations

According to the Post, the group’s discussions are being facilitated by the “Vaccine Integrity Project,” a new initiative at the University of Minnesota, which includes “vaccine manufacturers, health insurers and medical associations.” The group is funded by iAlumbra, a nonprofit founded by Walmart heiress and billionaire philanthropist Christy Walton, known for her anti-Trump advocacy.

Former U.S. Food and Drug Administration (FDA) Commissioner Margaret Hamburg and Dr. Harvey Fineberg, former president of the Institute of Medicine and current president of the Gordon and Betty Moore Foundation, co-chair an eight-member steering committee leading the initiative.

In an op-ed published in STAT News, Hamburg and Fineberg said the project will use “the best available evidence” to “safeguard vaccine policy, information and utilization.”

When the group was launched, Michael Osterholm, Ph.D., a member of the COVID-19 Advisory Board under the Biden administration, said it was not intended to serve as a shadow or parallel version of the ACIP.

However, according to today’s report from the Post, that intention appears to have changed.

Dr. Anne Zink, member of the Vaccine Integrity Project, told the Post that having each state set its own recommendations is “not ideal” and that instead, the major medical associations should make recommendations.

Medical associations participating in the Vaccine Integrity Project talks include the American Academy of Pediatrics (AAP), the American Academy of Family Physicians, the American College of Physicians, the American Pharmacists Association, and the National Foundation for Infectious Diseases, the Post reported.

In her op-ed, Chu also named the American College of Obstetricians and Gynecologists (ACOG) as a key group advising alternative vaccination policy.

Lyons-Weiler noted that AAP has received millions of dollars in grants from Merck, Sanofi and Pfizer, and that ACOG has endorsed products from its sponsors without conducting any independent review.

ACOG also took $11 million from the CDC to push the COVID-19 vaccines on pregnant women.at vaccine guidance is rigorous, independent, and truly in service to the health of the American people — not corporate interests.”

The Post reported that Nixon also called one of the new coalition’s leading organizations “a self-appointed echo chamber masquerading as oversight.”

Under Kennedy, the CDC has changed its guidance on COVID-19 vaccines for pregnant women from recommended to “no guidance.”

One member of the Vaccine Integrity Project, Asa Hutchinson, former Republican governor of Arkansas, noted that beyond changes to COVID-19 vaccine recommendations, no other changes have been made to vaccine policy since Kennedy took office.

In the upcoming meeting this week, ACIP is set to vote on RSV (respiratory syncytial virus) immunization recommendations for pregnant mothers, babies and young children.

The committee will also vote on the mercury-containing flu vaccine, and will discuss but not vote on other vaccines, including COVID-19, chikungunya, anthrax and MMRV (measles, mumps, rubella, varicella).

Related articles in The Defender

Jun 242025
 

The Last Selection was:    For Your Selection JUNE #3 2025         

We are crossing a bridge analogous to the one crossed by humanity from

  • belief The Earth is Flat    to
  • belief  The Earth is Round  (spherical).

 

READ  this ONE POSTING  and KNOW

2017-11-02   How long does it take for a newborn’s liver to mature? What are the consequences of a damaged liver? Why do Americans and Canadians start the Hepatitis B vaccine on day 1 or 2 of birth?      https://sandrafinley.ca/?p=19952

About the liver.    This is so critical.  I do not understand.   Surely,  people in the medical profession would know this.

– – – – – – – – – –

2025-06-24 For Your Selection June #4 2025

– – – – – – – –

SHOW-DOWN

2025-06-24 Washington Post Reports on  Plan to Vaccinate All Americans, Despite RFK Jr.   Opposition is from Vaccine makers, pharmacists, professional . . .

– – – – – – – –

INSERT, June 6th.    With many thanks to Shirley:

Sent: June 24, 2025
To: ‘Sandra Finley’

Hi Sandra,

I read Suzanne Humphries book some time ago and really enjoyed it – I particularly liked historical research. In doing family research I sometimes get the death record for infants or young people of interest and I wonder how many died because of vaccines, but had listed convulsions or something like that as cause of death.

You might want to alert people to Roman’s substack as well  https://romanbystrianyk.substack.com/ . I didn’t see it listed but I may have missed it. People tend to forget about him but he actually had accumulated a lot of the historical information, if I remember correctly.

I was disappointed that the 10th anniversary edition did not improve on the graphs, but colour ones are on a website. In a recent interview Suzanne just came right out and said she was anti-vax. She wasn’t going to beat around the bush on that anymore. So nice to have someone of her caliber take a stand like that.

I went back and checked on Tamara Ugolini’s article on Dr David Martin and she has finally corrected it. Maybe she got more than one email about it – so that was good. I find Martin quite interesting to listen to. He did a testimony for the NCI. His message has remained the same.

I know you didn’t like the last article I sent written by Miri Finch. However, I thought it provided an interesting hypothesis and we will see if she is right or partly right. I didn’t expect you to post it because it was “way out there” for most people. I think it was when she mentioned the movie that was made about Andy Wakefield starring Hugh Bonneville that really got me thinking she was on to something. I like her articles in general. She is one of the very few people I read who talk about news items that may be staged or fake. You never have to believe people, but you can always examine their evidence and reasoning – there is often some quite good research involved. I started finding and vetting these people after the fake Trump assassination attempt – the one where the bullet “grazed” his ear. People actually believed that. I must say I am quite tired of all the lies and deception we are bombarded with all the time.

Thanks for the links you send out, I do appreciate them.         /Shirley    (end of Insert)

– – – – – – – – – – – – – –

SANDRA SPEAKING:

I have now read Dr. Suzanne Humphries’ and Roman Bystrianyk’s  book:

  • Dissolving Illusions”  (published in 2023)
  • Sub-title “Disease, Vaccines and the Forgotten History
  • Companion and Reference
  • the 10th Anniversary copy of the original book (2013)

Not too long ago, lethal infections were feared in the Western world. Since that time, many countries have undergone a transformation from disease cesspools to much safer, healthier habitats. Starting in the mid-1800s, there was a steady drop in deaths from all infectious diseases, decreasing to relatively minor levels by the early 1900s. The history of that transformation involves famine, poverty, filth, lost cures, eugenicist doctrine, individual freedoms versus state might, protests and arrests over vaccine refusal, and much more.

Today, we are told that medical interventions increased our lifespan and single-handedly prevented masses of deaths. But is this really true?  Dissolving Illusions details facts and figures from long-overlooked medical journals, books, newspapers, and other sources. Using myth-shattering graphs, this book shows that vaccines, antibiotics, and other medical interventions are not responsible for the increase in lifespan and the decline in mortality from infectious diseases.

If the medical profession could systematically misinterpret and ignore key historical information, the question must be asked, “What else is ignored and misinterpreted today?” 

Perhaps the best reason to know our history is so that the worst parts are never repeated.

Sandra speaking:

The information in “Dissolving Illusions”   is collected and ordered from various historical sources.   An essential question is  “What was going on in the society at the time of the various epidemics in various countries?”

  •  There’s a “TIME-LINE” of newspaper clippings and reports  that starts when vaccinations were known as inoculations.
  •   There’s a section of “Doctor’s Quotes”.   Who was saying what  at different times  along the Time-Line.
  •   There’s a section on “Vaccine Tragedies”
  •   A  Royal Commission on Vaccination (May 1880)
  •   Think what you may.

– – – – – – – – – – – – –

POSTINGS from my blog WITH DR. SUZANNE HUMPHRIES    (In reverse, back to 2014.  there’s more on the internet.)

Also,   Dr Humphries joined the CHD Bus (Polly Tommy)  starting in 2016.  The bus criss-crossed the U.S. collecting the stories of  vaccine-injured children and their families.   It was a huge amount of work and made a huge contribution to people’s understanding of the tragedies,  the inhumanities,  the lies,  and the cover-ups.

– – – – – – – – – – – – –

2025-06-05 Blowing the Lid Off SIDS, Dr. Pierre Cory with host Steve Kirsch

APPENDED LIST:   VACCINES  – – SOME POSTINGS FROM MY BLOG.

2020-06-10 If I am making a choice about a vaccine, I want to know this  (WHAT ARE THE INGREDIENTS OF VACCINES?.)     https://sandrafinley.ca/blog/?p=25074

2025-04-09 8-Year-Old in West Texas Died From Hospital-acquired Pneumonia, Medical Records Show    https://sandrafinley.ca/blog/?p=31342

2025-05-23 I’ve been waiting for years for this – – a film that tells the Simpsonwood story    https://sandrafinley.ca/blog/?p=31536

2025-06-06 Simpsonwood. CHD   https://sandrafinley.ca/blog/?p=31658

 

2025-06-09 RFK Jr. Removes All Members of CDC Vaccine Advisory Committee

2025-06-06 Their Babies Died Suddenly in Their Sleep. Police Are Charging the Parents With Felonies for Not Placing Infants on Their Backs. Brenda Baletti, CHD

2025-06-03 posted. Covid. U.S. Senator Ron Johnson on podcast of Bret Weinstein (DarkHorse)

2025-05-29 UPDATE: Includes the inspirational ‘Moms Across America’ Plus the Update on ‘Double Tragedy’: Twins’ Deaths Likely Caused by Vaccines, Not Parents. On May 1, Dallas and Tyson, fraternal 18-month-old twins, were found dead by their mother after receiving the Hepatitis A, flu and DTaP vaccines on April 23. Police are investigating the parents, but Dr. Pierre Kory, who reviewed the twins’ medical records, told CHD.TV that, unfortunately, vaccine-related sudden infant deaths are “as common as the day is long.” by Suzanne Burdick, Ph.D.

2025-06-18 New CDC Vaccine Panel to Vote on Mercury in Flu Shots. The committee will also vote on RSV vaccines for pregnant mothers, babies and young children at its meeting next week — Suzanne Burdick, CHD

 

 – – – – – – – – –    OTHER SELECTIONS  – – nothing to do with VACCINATIONS

2025-05-16 Documentary “Manufacturing the Threat”

2025-06-18 Reclaim the Net.

2025-06-09 Dr Phil interviews Tom Homan. Reveals What ICE Found in LA Crackdown.

Transitioning or Maturing into wisdom

The film “1971”

2025-06-17 The Corbett Report June 18

 

Jun 232025
 

There is more to say about mental telepathy,  but later.    /Sandra

In the Eisenstein posting, excerpt below, there is a link Telepathy Tapes.   (https://www.youtube.com/watch?v=oci3qhC-yzM)

RELATED TO    “The INCREDIBLE TRUE Stories Behind ‘The Telepathy Tapes”
EXCERPT:

There is, however, a deeper level to what is happening through the autism phenomenon. In adapting to their condition, autistic people often develop gifts, both mental and emotional, that society needs right now; for example, the abilities of the Spellers described in the podcast the Telepathy Tapes. More generally, in adapting to the specific challenges of each stage of civilization, human beings develop the capabilities necessary for humanity to move to the next stage.

Each one of us is soul made flesh; Life made human. If a tree grows in rocky soil, shaded by other trees, and it twists and reaches for the light, we do not say it is a bad tree for being misshapen. It is doing what life does. Life wants to live. Life adapts to overcome all difficulties. Life evolves because of its difficulties.

Anyone who thinks that their own virtue and willpower distinguishes them from the obese, the depressed, the addicted, the poor, the lazy, the ignorant, the unjust, or the violent has a humbling lesson in front of them.

When a child is injured by vaccines or other environmental insults, and the life within him takes a form different from the rest of us, this is cause for celebration — life lives! — not shame. Yet that does not justify the injury.

The autistic are not the only ones who’ve suffered injury from the world-destroying life-destroying Machine. The modern way of life, birth, child-rearing, and death, its sundering of ties to community and nature, its entrenched cycles of trauma, its denial of spirit, its relentless artificial scarcity, and its pollution of the body and the environment with toxic chemicals compose the rocky soil and occluded sunlight in which we have all grown. The life in each of us adapts to these conditions as best it can.

We call this basic truth compassion. “But for the grace of God, I too would be autistic. I too would be obese. I too would be addicted.” Or, “I too would be a migrant. I too would be on welfare. I too would drop out of school.” And even, “I too would be a criminal. I too would be greedy. I too would cheat and lie and steal and do others harm.” Not only would I, but surely I have, in some way and form. As Thich Nhat Hanh said, “I am the pirate.” What is in you, is in me, some echo of it, some holographic trace of it. Let he who be without sin cast the first stone.

Those we stone with our insults and shaming and denunciation are ourselves. Understand a person’s backstory, and you will realize, “That could have been me.” None of us are made of better or worse stuff than the rest. We all are life, doing what life does in the circumstances it is in. Yet neither is anyone a helpless victim of circumstance. That’s because life is not static. We grow new capacities in evolving within and against trying conditions, until they no longer imprison us but become the material for creative choice. That is the moment when the truth of “It is not your fault; you are victim of forces beyond your control” gives way to a new truth: “Stop feeling sorry for yourself. You are no longer a prisoner of your past, you the author of your future.” The former had been true, but no longer. From the victim, comes the master. From the illness comes the medicine.

So, when I meet someone profoundly challenged by injury, illness, tragedy, or persecution, I am always curious. What capacities have been forged in the crucible of your suffering? Again and again, I discover generosity among the impoverished, inner freedom among the incarcerated, compassion among the judged, kindness among the brutalized, joy among the bereft. Sometimes it is hard to see, just a glint of something still forming. Sometimes it is radiant like the sun.

It is by those who have grown strong by overcoming the injuries dealt to them by civilization that a new kind of civilization will be born.

 

 

Jun 202025
 

 

June 11, 2025

Pediatric Perspectives: Risking Everything

You can learn a lot by having conversations with people — especially those you may disagree with. Doing this has helped shape the lives of physicians like Paul Thomas, M.D. (retired) and Suzanne Humphries, M.D.

Many have even walked away from their practices, given up their licenses and put just about everything else at risk because of what they were challenged to consider. Covered in this episode of “Pediatric Perspectives” are some of the topics that have arisen from these difficult conversations. It’s a show that you won’t want to miss!

Watch below:

 

 

 

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