Archive for the ‘Activism’ Category

Medicine Betrayed: A Conversation With Whistleblowers

Analysis by Tessa Lena

STORY AT-A-GLANCE

  • In this explosive interview, Dr. Venu Julapalli, Dr. Mary Crow, and Owen Robinson (RN) talk about all the irrational, tragic, and harmful policies they have experienced at the Houston Methodist Hospital in Texas
  • Dr. Julapalli filed a lawsuit at Houston Methodist after they introduced vaccines mandates in 2021
  • He also started an internal listserv for physicians at the hospital, and he observed first-hand the tremendous levels of fear that the doctors felt over speaking out
  • As conveyed to Dr. Julapalli by a well-respected anonymous physician, she was offered by the Chief Medical Officer at Houston Methodist to secretly fake the vaccine
  • Owen Robison, who worked as a nurse at the ICU until he was terminated for declining the booster, is convinced that the mandates were the main reason for staffing shortages
  • According to him, due to shortages, vaccinated and boosted ICU nurses were forced to come in to work and look after patients while sick

Recently, I had a chance to interview three courageous whistleblowers at the Houston Methodist Hospital in Texas. What they had to say was a mind-blowing condemnation of the state of our “healthcare” system.

We talked about the COVID vaccine mandates that Houston Methodist Hospital “spearheaded” in the U.S. back in 2021, about vaccinated and boosted nurses getting “COVID” anyway — and being forced to come in to work at the ICU while sick with fevers — and about the tremendous fear that the doctors felt over speaking out.

We also talked about a top executive at Houston Methodist allegedly offering the physicians in his inner circle an opportunity to fake the vaccine — while publicly touting COVID injections as a necessary and life-saving measure.

Now, philosophically speaking, it is not that shocking to me as a Soviet expat. That is how things were universally done in my old homeland — public and private policy, so to speak — but seeing such blatant, time-warped signs of all-permeating corruption and censorship-driven behavior in America, as if I were back in the USSR, is bizarre. But first things first. Let me introduce the Houston Methodist whistleblowers.

Dr. Mary Crow

Dr. Mary Crow is a well-respected oncologist and hematologist in Texas. She received her medical training at Baylor College of Medicine and has been practicing for over 30 years. In the 1990s, Dr. Crow was a Chief Oncology Fellow at the MD Anderson Cancer Center.

She is a member of the American Society of Clinical Oncology (ASCO), the American Society of Hematology (ASH), the Harris County Medical Society (HCMS) and the Texas Medical Association (TMA).

Dr. Crow has been very outspoken about the not-so-scientific nature of the “COVID response” from the get-go. When Houston Methodist introduced the mandates for physicians, she applied for a religious exemption. As a result, she was not granted an exemption, and she lost he medical privileges at Houston Methodist.

(To clarify, the term “medical privileges” stands for the right of a physician to work at a hospital. In Texas, physicians are not considered hospital employees but independent professionals who work with hospitals where they have “privileges.”)

Dr. Venu Julapalli

Dr. Venu Julapalli is a gastroenterologist in Houston, TX. He received his medical degree from Baylor College of Medicine in in Houston, TX, and has been practicing for more than 20 years. In 2005, he founded a groundbreaking gastroenterology private practice in Houston, TX.

Together with his cardiologist brother, Dr. Vinay Julapalli, Dr. Venu is on a quest to bring the heart back to modern medicine and to restore the sacred relationship between patients and doctors. Both Dr. Venu and Dr. Vinay have been on this quest for a long time.

In 2021, after Houston Methodist Hospital mandated COVID injections for physicians, Dr. Venu Julapalli’s religious exemption was denied, and his privileges at the hospital were suspected and eventually revoked. In the summer of 2021, he filed a lawsuit. His lawsuit is still pending. If you are looking to learn more about Dr. Venu Julapalli and his lawsuit, I interviewed him in detail about it in August 2021.

Another thing that he did in 2021 was organizing an internal listserv for the “medical staff” (physicians with “medical privileges”) at Houston Methodist. The list initially consisted of about a thousand physicians. The purpose of the listserv was to have open conversations about what was going on. A few doctors, such as Dr. Mary Crow, were very outspoken, and questioned the rationale behind the official “COVID response.”

Most weren’t outspoken at all though, even on the internal listserv. Many were afraid to talk. They had concerns — which they shared privately with Dr. Julapalli — but they were too scared to speak loud.

When talking about it, Dr. Venu Julapalli takes no prisoners and makes a great point: If all the doctors who had sincere concerns found the guts to voice their concerns out loud, we wouldn’t be dealing with the nightmare that we are dealing with today.

Conclusion? We have a free will for a reason, and our choices actually matter! Our courage matters. The world takes the shape of our collective choices, and at any moment when we feel scared, or insignificant, or powerless, we are just making the world smaller.

Owen Robinson

Owen Robinson is a registered nurse who has been working in critical healthcare for twelve years. He has been taking care of patients all through 2020 — until he was terminated for declining the booster.

Owen got the original series of COVID injections early on. He did it based on the fact that the general understanding in his circles was that vaccines were good, and safe, and of course properly tested. What also impacted his choice at the time was the fact that he had seen people dying with COVID symptoms in the ICU with his own eyes. According to Owen, the number of people dying during that time was truly larger than what he had seen before COVID.

However, once he himself got sick and tested positive for COVID — and especially when he saw the vaccinated and boosted nurses developing COVID symptoms and working sick — he realized that the claim of “doing this for patient safety” was not panning out.

He also saw that the procedures were organized in such a way that the vaccinated and boosted nurses were almost more likely to be working sick and potentially “spread COVID” than the perpetually tested nurses with religious exemptions.

Vaccinated and Boosted Nurses Forced to Work While Sick

The straw that “broke the camel’s back” for Owen Robinson was when he saw two vaccinated nurses forced by their superiors to come in sick, with fevers — and one of the nurses was so sick that she had to spend the day sitting at her desk with her head down, while the new trainee nurse was doing her job.

Another nurse, not in the ICU, passed out on the hospital floor in the middle of her shift and had to be taken to the emergency room. Allegedly, when it happened, she was taking care of a patient who was unstable, and, based on what Owen had heard, the situation impacted the patient’s condition. In his own words:

[When Houston Methodist announced the mandate], I didn’t agree with the mandate, but I’d already been vaccinated, so I was able to keep my position. Then about the same time that the CDC dropped the … the requirement for nurses … first it was 14 days from being positive for COVID that a nurse could come back into work. Then it went to 10 days.

And about that time, I got COVID. I was positive for COVID. I was out for work, they dropped it from 14 to 10 days, and I told them I’m not coming back in with symptoms […]. If I have symptoms, I’m not coming back in with COVID. And they were like, Okay, well, we’ll see. And they didn’t make me come back in at that time.

So then I came back to work, people are getting sick people have been vaccinated, fully vaccinated with the booster … they had they mandated the booster. [… I refused to get the booster after my exemption expired, and I was suspended and then terminated].

The thing that that caused me to really walk away, was when I came back to work, not only were the fully vaccinated and boosted nurses getting sick, but the CDC dropped that window to five days for nurses to come back in after they tested positive. And the director of our ICU forced two nurses to come back into the unit, sick with fevers and symptoms, and to take care of patients in the ICU, possibly immunocompromised patients in the ICU.

One of the nurses was so ill that she sat at the desk with her head down on the desk most of the day. And she had a trainee, a new nurse who was doing all of her work for her and taking care of her patients for her. And it would just not sit well with me. I didn’t think that was right. I didn’t think it was safe.

They made us … when we applied for an exemption, they made us sign this, this list, that said, I know that I’m not safe for my patients, I know that I’m not safe for my co-workers, because I’m refusing to get this vaccine …

I know that, you know, all these things that that you had to agree that that didn’t even make sense and were very negative, basically … and you had to sign that just to get an exemption. And then the people who did get the exemptions had come in and swab every week.

And then of course, a lot of some people got religious exemptions, and then when they came out with this latest bivalent vaccine, then they pulled all of those religious exemptions for people and fired them anyway. So it was just, it was just terrible situation.

“Air Vaccines”

One of the most explosive parts of the interview was the segment where we talked about how allegedly, a top executive at Houston Methodist was offering select physicians “air vaccines,” a way to fake their vaccination status to circumvent the mandates — all while publicly promoting the mandates as a necessary and noble safety measure.

That, now, brings me straight back to my childhood because this is exactly how things were done in the USSR. Here is the segment of the transcript:

Tessa Lena:

And so now we are coming to the juicy part of the interview, the fake, the air vaccines. So from what I understand the very top management at the hospital at Houston Methodist, the very management that was mandating the vax … […] and promoting it as a safety precaution, a very important one, the very same people were allegedly offering up fake vaccines to the people they liked or trusted … to the physicians they liked or they trusted, to their close circle? So let’s talk about that.

Dr. Venu Julapalli:

So let me give a little context to this. In the course of the exchanges that we were having on the listserv, I would get private messages from folks who would just talk about various things. It was either for support or some question.

So one of those individuals, a colleague, messaged me, she had gotten her initial vaccination. And then Methodist mandated the booster. This was in February 2022. She didn’t want to take the booster. So she filed her religious exemption, it was denied. And so she basically was asking, well, what am I supposed to do now.

And in the course of that conversation, she wanted to talk to us, me and my brother, who’s also on staff at Houston Methodist, The Woodlands. And so we had a coffee meeting, meeting with coffee, and she told us that one of her colleagues, who is the Chief Medical Officer at Houston Methodist at The Woodlands offered her the opportunity to fake the vaccine.

Now, this is, the person who’s being offered this is well respected. Obviously, the Chief Medical Officer wants to keep her there. And she told us that she was taken aback and asked the Chief Medical Officer, if this is something that was asked or offered before, or she was the first one that was offered to and, and the response apparently, that he said that, that he could neither confirm nor deny whether it was offered before.

Now, of course, she didn’t take up the offer. And she ended up getting a religious exemption approved shortly after all went forward. But that’s what apparently is going on.

Now. I don’t know how pervasive this is. I don’t know how extensive this is. I don’t know where this stops, apparently was something that was being done within the … the system, but I don’t know how it was happening. But to me, it just is a culture issue. I mean, this is the Chief Medical Officer at this institution, the institution that started it all on this whole vaccine mandate.

My understanding is that this particular person didn’t even approve of the booster, he no longer thought that this was, this was a good policy. And … and even … he even expressed that. So in that respect, I mean, it’s not really even about the Chief Medical Officer, he’s obviously trying to help somebody out and … and keep somebody that is valued and respected. What kind of culture puts a person in that kind of Catch-22 situation?

I mean, I wouldn’t do it if I were in that situation, but he’s put in that situation. And he’s compelled to, you know, offer somebody the Underground Railroad.

There’s something deeply wrong with the culture, when that very policy that was established by this institution, that they put all of their brand and all of their reputation behind … in fact, in their own words they want to lead the country on … has one of its own executive officers giving somebody a way out?

Tessa Lena:

Well, it poses several questions. One, the most important one of them, the one that is straight in our faces is that if somebody truly believed that the vaccines are needed for safety, then one would not offer a fake one because then one would be afraid for his own life, right? […] You’d want everybody to get it. If you’re genuinely thinking that that’s what’s needed to protect our health. And his own, for that matter.

Dr. Venu Julapalli:

I mean, that’s … that’s such an obvious thing that we actually take that for granted. But you’re absolutely correct. I mean, that leads … that really calls up this point, how do we know anybody’s done anything? I mean, there was no verification process. I mean, if you were just … if you said you were vaccinated, you were considered vaccinated.

So, you know, Methodist will keep going out there, the CEO, Dr. Marc Boom, would go out onto CNN, MSNBC, saying we’re 99% vaccinated. Well, how does he know that? I mean, how does he know who actually took it? Or who actually faked it? How do we know anything at that point?

Tessa Lena:

Well, theoretically, if you decided to be dishonest and not fight the honest fight but instead say that you got the vaccine, just say it, would anybody check your records, your … your card, your CDC card or anything like that?

Dr. Venu Julapalli:

As far as the medical stuff was concerned, no.

Tessa Lena:

So chances that some people, just by human nature, that are considered vaccinated on the system now, that maybe they didn’t even get it, they just said it? It’s possible?

Dr. Venu Julapalli:

Oh I think it’s possible, yes. And how pervasive is it … is the next question on my mind.

Tessa Lena:

I mean, the absurdity of it is just stunning. And so, and as far as you know, this, air vaccine was offered on the booster mandate stage of it, right?

Dr. Venu Julapalli:

That’s when we were informed of the story. So that … that leads to another question. Well, how, when was the system like this begun? Was it begun at the very beginning? Did it only come on later, when, you know, other information had come out, and people were getting more reluctant to do this?

I can certainly say that by the time of the booster mandate, in terms of what I was getting, because we actually surveyed this on the listserv, the medical staff had started originally, in vast majorities of support for the first series.

So we were in the minority, those of us who didn’t, who felt that mandatory vaccination was not a good policy, we were in the minority. By the time of the booster mandate, which was February 2022, that tide had completely turned.

I mean, we had in our survey, 75 to 80% of people saying that the booster mandate and termination of privileges as a result of not following that mandate was not a good policy. Of course, they don’t say that in public and on the record, but they would say that anonymously on a survey.

By the way, per Owen Robinson, unlike doctors, the nursing staff at Houston Methodist had to actually “prove” their vaccination status — which is to say that the randomness of the entire affair was truly Soviet-like.

Burnouts, Mandates and Staffing Shortages

For months now, we’ve been hearing from the mainstream media that the staffing shortages in healthcare are due to “burnout.” According to Owen, while there was some burnout, it was mostly due to the poor administrative management of the situation. He believes that the hospital became truly “overwhelmed” after the vaccine mandates caused many employees to quit, and the staffing shortage became severe.

Also, during the “Omicron” wave, a lot of the people occupying COVID hospital beds didn’t have any symptoms at all or only mild cold symptoms. The reason for that was that the hospital was testing all patients for COVID, even if they came to the hospital with a broken leg. And then, if they tested positive, they would be hospitalized and given a course of Remdesivir.

He notes that while he is a nurse and it’s not his place to diagnose, there were many patients without symptoms or with light symptoms treated for COVID as a part of this protocol, and since the beds were occupied by the people who weren’t very sick at all, the ones who needed to be hospitalized had a harder time getting hospitalized. A mind-twister, indeed! Dr. Crow adds:

“The hospitals had no surge capacity, Tessa, and they have … haven’t had it for 10 or 15 years. The summer before COVID, any one of these hospitals in The Woodlands was on drive by. They had no available beds two days out of seven in the summer. And then when they decided to accept limited trauma, it got worse.

So this idea that the hospitals were overwhelmed was ridiculous, because they were already overwhelmed, all right. These hospitals operate at 98% capacity on a given day.”

Fertility Concerns

Another thing that Dr. Crow mentioned in the interview was her concerns over the effect of the COVID injections on fertility. In her own words:

I see a lot of young women for severe iron deficiency […] we talked about their symptoms, a lot of menstrual irregularities, difficulty getting pregnant, miscarriages, and I thought, well, maybe they’re under stress, everybody’s under stress. And you started hearing this out in … among the vaccinated certainly as the boosters started rolling out.

And if you notice in all the highly vaccinated countries, Iceland, Ireland, UK, there is no baby boom. There’s no baby boom. In fact, there is a drop in babies and this was occurred in Germany and in the EU as well. So I remain very concerned about this moving forward.

Because in the Japanese bio localization study, these lipid nanoparticles bio located in the ovaries, the testes, the spleen, the bone marrow in the liver, okay. And in none of the animal trials, or the vaccinated, the offspring of the vaccinated animals went on to go and get pregnant, they were all killed after nursing.

So I think there is a ticking time bomb here. Because if you look at Africa, which is only 6% vaccinated, they’re not having any fertility problems. And they’re having … they’re having no excess mortality. And they’re doing … and they’re having no COVID.

So there’s something that’s very wrong here, when you actually get into the data. And this is based on the data that these countries have released when they release it. All right, you got to look forward a little bit. But I would just ask my OBGYN colleagues, are you seeing a baby boom? Because every time you lock up human beings, even in the concentration camps, people got pregnant and had babies, and that’s not really happening.

Conclusion

It makes me wonder what our life would be like today if every person — every doctor, every journalist, ever lawyer, every artist, every scientist, etc. — chose to be brave.

There is an art and science to bullying. There is a technique to driving people crazy. There is a methodology to elevating the sense of helplessness and obfuscating the power that we truly have from the moment we are born.

I pray that all this pain we’ve been through is not in vain, and that the ones who have been timid up to this second, connect to their inner lion and choose to be new and brave from now on. I pray that their inner lion guides them on the path of fixing the wrongs that they allowed to happen on their watch. The pain needs to be healed. It is never too late to be brave. It is never too easy to be brave but it is also never too late. There is work to do. Can you see your inner lion? I can.

Source

About the Author

To find more of Tessa Lena’s work, be sure to check out her bio, Tessa Fights Robots.

And the whistleblowers just keep on coming:

Published Writings Exposing the CDC’s False Lyme Disease Narrative

https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/

Published writings exposing the CDC’s false Lyme disease narrative

Carl Tuttle

Hudson, NH, United States

MAR 17, 2023 — 

Additional information sent to Mathematica Policy Research. It should be noted that there hasn’t been a single response from anyone at Mathematica or the CDC. 

Truth does not mind being questioned. A lie does not like being challenged!

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: “achen@mathematica-mpr.com” <achen@mathematica-mpr.com>, “info@mathematica-mpr.com” <info@mathematica-mpr.com>, “pdecker@mathematica-mpr.com” <pdecker@mathematica-mpr.com>
Cc: “lwx1@cdc.gov” <lwx1@cdc.gov>, “frederick.chen@ama-assn.org” <frederick.chen@ama-assn.org>, “gmarx@cdc.gov” <gmarx@cdc.gov>, “acoyne@mathematica-mpr.com” <acoyne@mathematica-mpr.com>, “jconstantine@mathematica-mpr.com” <jconstantine@mathematica-mpr.com>, “ctrenholm@mathematica-mpr.com” <ctrenholm@mathematica-mpr.com>, “tbarnes@mathematica-mpr.com” <tbarnes@mathematica-mpr.com>, “sboudreau@mathematica-mpr.com” <sboudreau@mathematica-mpr.com>, “jdevallance@mathematica-mpr.com” <jdevallance@mathematica-mpr.com>, “sara.berg@ama-assn.org” <sara.berg@ama-assn.org>, “jack.resneck@ucsf.edu” <jack.resneck@ucsf.edu>, “jack.resneck@ama-assn.org” <jack.resneck@ama-assn.org>, “todd.unger@ama-assn.org” <todd.unger@ama-assn.org>, “jon.burkhart@ama-assn.org” <jon.burkhart@ama-assn.org>, “karen.kmetik@ama-assn.org” <karen.kmetik@ama-assn.org>, “sanjay.desai@ama-assn.org” <sanjay.desai@ama-assn.org>, “william_henderson@paul.senate.gov” <william_henderson@paul.senate.gov>
Date: 03/17/2023 11:48 AM
Subject: Published writings exposing the CDC’s false Lyme disease narrative; “Hard to catch and easily treated”

Mathematica
Princeton, NJ
Attn: Arnold Chen, Senior Researcher

Dear Dr. Chen,

Now that we know that the Covid lab leak theory being a “conspiracy theory” was a lie and the “15 days to stop the spread” was a lie and “masks work” to stop the spread was a lie and “vaccine mandates will stop the spread” was a lie and “natural immunity is a myth” was a lie and the “there is no side effects” was a lie and the “safe and 100% effective” was a lie then you can pretty much bet that “chronic Lyme does not exist” is a lie. Post Treatment Lyme Disease Syndrome is simply a fabricated medical condition disguising treatment failure because a chronic relapsing  seronegative disease does not fit the business model of vaccine development, patent royalties and pharmaceutical profits. All this suffering for the sake of a vaccine. Just like the current mismanagement of Covid … all for the sake of a vaccine. It should be blatantly obvious to everyone; pharmaceutical profits over lifesaving care. Suppressing evidence of persistent infection after antibiotic treatment for Lyme disease is criminal.

Patient testimony across America is describing a disease that is destroying lives, ending careers while leaving its victims in financial ruin.

The false Lyme disease narrative “Hard to catch and easily treated” propagated by the CDC for nearly three decades has been exposed in countless books; first and foremost, frontline treating physician Dr. Kenneth Liegner’s 892-page book:

In the Crucible of Chronic Lyme Disease: Collected Writings & Associated Materials 
by M.D. Kenneth B. Liegner

“In the fullness of time, the mainstream handling of chronic Lyme disease will be viewed as one of the most shameful episodes in the history of medicine because elements of academic medicine, elements of government and virtually the entire insurance industry have colluded to deny a disease.” -Kenneth B. Liegner M.D.

Cure Unknown: Inside the Lyme Epidemic (Revised Edition with New Chapter)
by Pamela Weintraub

Gone in a Heartbeat: A Physician’s Search for True Healing 
by Dr. Neil Spector

Lyme Madness: Rescuing My Son Down The Rabbit Hole of Chronic Lyme Disease.
by Lori Dennis

Bite Me: How Lyme Disease Stole My Childhood, Made Me Crazy, and Almost Killed Me
by Ally Hilfiger, Tommy Hilfiger – foreword, et al

The Opposite of Fate by Amy Tan

Suffering the Silence: Chronic Lyme Disease in an Age of Denial
by Allie Cashel, Mandy Kaplan, et al.

Believe Me: My Battle with the Invisible Disability of Lyme Disease
by Yolanda Hadid, Daisy White, et al.

When Your Child Has Lyme Disease: A Parent’s Survival Guide
by Sandra K Berenbaum, Dorothy Kupcha

But She Looks Fine: From Illness to Activism
by Olivia Goodreau

Lyme disease: Can Justin Bieber recover?
by Richard Rawls

What Lurks in the Woods: Struggle and Hope in the Midst of Chronic Illness, A Memoir
by Nicole Bell

Australian Lyme Crimes: The Global Disgrace
by Julie Mellae

Starving to Heal in Siberia: My Radical Recovery from Late-Stage Lyme Disease and How It Could Help Others
by Michelle B. Slater PhD, Carol Jacobanis, et al.

Lyme Rage: A Mother’s Struggle To Save Her Daughter from Lyme Disease
by Mindy Haber

Silent Suffering: Finding God’s Faithfulness in Chronic Lyme Disease
by Lauren Murphree and Andrew Murphree

Holding Hope: One Family’s Odyssey through Lyme Disease and Psychosis
by Marabai Rose

Out of the Woods: Healing from Lyme Disease for Body, Mind, and Spirit
by Katina Makris, Richard Horowitz, et al.

Dear Lyme Disease: Transforming Your Pain into Purpose
by Wendi M. Lindenmuth, Megan Hudgins, et al.

Shadows of Lyme Disease
by Ron Landis

Ticked Off: A Physician Shares How He Beat Lyme and Got His Life Back
by Dr Gordon Crozier

There’s a Deer at the Door and a Cow in the Mudroom: Learning to Live while Living with Lyme
by Jamie Bennett

THE GIFT OF LYME DISEASE AND CO-INFECTIONS
by Suzen Chan

Fighting for My Life: How I Found God and Beat Lyme Disease
by Patrick Collins

Tickled Imagination: A teenager’s reality living with undiagnosed Lyme Disease
by Lauren Kingsly

Not If, When: Lyme Disease in Verse
by Gail Tierney

Cancer on a Harley – Or is It? Lyme Disease
by Lisa Torbert

It’s All In My Head: A Journey of Healing & Transformation Through Chronic Lyme Disease
by Joe Cusamano

A Twist of Lyme: Battling a Disease That “Doesn’T Exist”
by Andrea H. Caesar

Over My Dead Body: What I Learned During My Decade-long Journey to Heal from Lyme Disease and Coinfections
by Mary Lyn Hammer

In Limbo Over Lyme Disease
by Melanie S. Weiss

Summary:

We are dealing with a life-altering/life-threatening infection with faulty/misleading antibody tests, inadequate treatment, misguided medical training and absolutely no disease control whatsoever; a public health disaster.

Has Mathematica Policy Research been pulled into this crime against humanity while being paid by the CDC to propagate the well-established false Lyme disease narrative under the guise of “GUIDANCE”?

A response to this inquiry is requested.

Carl Tuttle
Hudson, NH

Pfizer’s Collusion With NIH: Repeal Bayh-Dole Act

The following information is imperative to understand and know as it directly affects Lyme/MSIDS patients.  It is a main reason why research regarding tick-borne disease is biased, controlled, stymied and will go absolutely no where unless the Bayh-Dole Act and other measures are repealed.   

You simply can not allow government scientists and agencies to own patents and profit where public health is concerned.

http://

The Impact of the Bayh-Dole Act

Conflicts of Interest: Pfizer’s Secret Collusion With the NIH

https://media.mercola.com/ImageServer/Public/2023/March/PDF/conflicts-of-interest-pfizer-nih-collusion-pdf.pdf

March, 21, 2023

Analysis by Dr. Joseph Mercola

Please watch the 6 minute Full Measure video here with investigative journalist Sharyl Attkisson as she reports the findings of watchdog group Open The Books on government scientists collecting royalty payments from Big Pharma while working on the tax-payer’s dime.

STORY AT-A-GLANCE

  • Under the 1984 Bayh-Dole Act, government scientists can collect royalties from drug companies for discoveries they make while working on the public’s dime
  • Taxpayers fund government research, while Big Pharma, the National Institutes of Health and NIH scientists keep all the profits
  • As a patent holder who profits from royalties, the NIH has a significant stake in regulations that impact patents and vaccine mandates, and may use its influence to benefit itself rather than the public
  • The NIH distributes $32 billion of taxpayer funds as research grants each year. As the largest federal grant-maker, the NIH has a monopoly on what research gets done and what doesn’t
  • Scientists vying for grants also recognize that in order to get funding, they have to play by the rules, and that means doing work that supports establishment narratives on public health policy

In late February 2023, Moderna agreed to pay $400 million to the National Institute of Allergy and Infectious Diseases (NIAID) for the patent it holds on Moderna’s mRNA shot.1

The patent process is a part of the COVID mRNA shots that the media haven’t really addressed and people in general don’t know anything about — probably because it’s a total racket. Based on internal documents and correspondence, it appears the NIAID funded the creation of SARS-CoV-2. At the same time, it patented and receives royalty payments for the “vaccine” against said virus.

The National Institutes of Health (NIH) is supposed to be the primary government agency responsible for public health research, but by the looks of it, it appears instead to be in the business of creating public health threats in order to profit from them.

And the agency itself isn’t the only one raking in profits. Many patents are held by individuals working at the NIH/NIAID. So, taxpayers fund research that may or may not work out, while Big Pharma, the NIH and individuals at the NIH profit from products that end up on the market. This is a clear conflict of interest that can hurt public health in any number of ways.

For starters, it incentivizes the NIH to support and promote potentially dangerous drugs, as we’ve clearly seen during the COVID pandemic. The NIH also has a significant stake in regulations that impact patents and vaccine mandates, and may use its influence to benefit itself rather than the public.

Conflicts of Interest Influence Public Health Policy

In the Full Measure video above, investigative journalist Sharyl Attkisson reports the findings of watchdog group Open The Books, which recently took a deep dive into “the issue of government scientists collecting royalty payments from pharmaceutical companies for discoveries made while working on your dime.”

According to OpenTheBooks.com founder and CEO Adam Andrzejewski, the NIH distributes $32 billion of taxpayer funds as research grants each year to an estimated 56,000 different entities. “That basically buys you the entire American health care space,” he says.

As the largest federal grant-maker, the NIH has a monopoly on what research gets done and what doesn’t, as it decides which scientists and projects get that money. Scientists vying for grants also recognize that in order to get a piece of that pie, they have to play by the rules, and that means doing work that supports establishment narratives on public health policy.

But that’s not all. The NIH is also gobbling up patents, which further weakens its incentive to protect and promote what’s truly in the public’s best interest due to the financial conflicts of interest that come into play.

How the Third-Party Royalty Complex Works

As explained by Andrzejewski, under the 1984 Bayh-Dole Act, government scientists can collect royalties from drug companies for discoveries they make while working on the public’s dime:

“Here’s how the third-party royalty complex works. You have a government scientist funded by taxpayers, and they work in a government lab that’s also funded by taxpayers. And when they have an invention [a drug, device or therapeutic] … the NIH … then licenses that invention … to the private sector.

And the private sector then pays royalties back to NIH. NIH then distributes those royalties on a royalty split schedule, back to the scientist. Details of those royalty payments to government scientists are kept as strictly held secrets.”

In fact, these royalty payments are kept under such closed wraps, scientists who receive them aren’t even required to divulge them on their financial statements, let alone to the public. Congress can’t even access those data.

In mid-June 2022, Sen. Rand Paul questioned then-NIAID chief Dr. Anthony Fauci about whether he’d ever received royalty payments from an entity to which he had given a research grant, and whether he or anyone else on the vaccine committee had ever received payments from vaccine makers.2 Fauci suffered one of his now-famous lapses of memory and wouldn’t answer.

NIH Fights to Shield Conflicted Parties

Paul’s questioning of Fauci came on the heels of a lawsuit filed against the NIH to obtain these payment disclosures. The lawsuit was filed by Open The Books in October 2021. But while the NIH eventually did release them, many of the most crucial pieces of information were redacted, and Paul’s attempt to get answers led nowhere. As noted by Andrzejewski:

“That lawsuit unearthed 3,000 pages of royalty payments to NIH scientists from 2010 to 2021. During that time, 2,407 government scientists received $325 million in secretive royalty payments, averaging out to more than $135,000 each.

But much is left unknown. NIH redacted or blacked out key details. We don’t know who paid it. We don’t know how much each individual scientist received. We can only see their names and count the number of times that each scientist received a payment.

And they also redacted the invention, the license number or the patent number … So, every single one of those individual, third-party royalty payments has the appearance of a conflict of interest …

We need to be able to follow the money. Unelected bureaucrats are running the entire American health care complex without any scrutiny. They’re basically telling the American people, ‘Sit down, shut up, pay up. We’ll run things.’ And that’s not how the federal government is supposed to operate.”

COVID Jabs Are Rife With Conflicts of Interest

Conflicts of interest also appear to have played a role in the U.S. government’s preferential treatment of Pfizer and Moderna during the pandemic. Pfizer was the first to receive government authorization for its COVID jab, and it just so happens to be part of an NIH royalty-sharing agreement.

Moderna also has such an agreement. What this all means is that the NIH helped invent certain technologies that went into these shots, and then licensed those technologies to Pfizer and Moderna in return for royalty payments.

So, the NIH has been making tens of millions of dollars from the COVID shots. Could that financial incentive influence the NIH’s stance on vaccine mandates? What do you think?

As you may recall, Johnson & Johnson’s COVID jab was vilified for causing blood clots, and the U.S. Food and Drug Administration even limited the authorized use of the Janssen shot to people over the age of 18 who have no access to Moderna’s or Pfizer’s jabs, and/or those who voluntarily opt for the Janssen shot, understanding the risks.3

Meanwhile, Pfizer’s and Moderna’s shots also cause blood clots, but neither of them was placed under restrictions. Instead, both were added to the U.S. childhood and adult vaccination schedules. Janssen wasn’t.

The NIH Royalty Cash Cow

The NIH’s secret royalties and the conflicts of interest these payments create were also addressed by “Rising” hosts Robby Soave and Briahna Joy Gray in a recent episode (video above). Alexander Zaitchik, author of “Owning the Sun: A People’s History of Monopoly Medicine from Aspirin to COVID-19 Vaccines,” also joined them on the program.

In Zaitchik’s view, the biggest scandal is not that government scientists are receiving royalty payments from drug companies but, rather, the intimate relationship that exists between government and “an industry that is using the monopoly system to price gouge the American people.”

“The NIH has basically abandoned its role to serve the public,” Zaitchik says, “and instead has become much too aligned with the industry and is an enabler, an accomplice and a protector of these monopolies. The vaccines are a point in case.

Government science was basically given, along with these massive research subsidies, through Warp Speed, to Moderna, for example. And there were no public interest provisions attached.

There were no pricing promises, there were no requests that technology be transferred [shared] with other parts of the world. It was basically a conveyor belt for private industry … So, for me, the real problem is NIH [being] fully aligned with industry on the monopoly question when public science is involved …”

Public Gets Fleeced Coming and Going

When public monies are being used for research, any scientific discoveries ought to be used for the public’s benefit, and the patents should remain public property with broad licensing rights.

This used to be the default position, but not anymore. In the 1970s, Big Pharma convinced Congress that this policy was slowing down innovation, and that if companies were allowed to claim exclusive rights to the patents, they’d be more apt to innovate. The Bayh-Dole Act was an outgrowth of this.

But we can now see why and how that doesn’t work. Public health is literally being sacrificed for profit, and since government agencies are in on it, there’s no one left to look out for the public’s interests.

Additionally, the public ends up getting fleeced twice. First, our tax dollars are being used to fund the research that private companies then lay claim to, and then we end up paying top dollar for the products we funded the development of, as there’s no price competition.

As noted by Zaitchik, while the Bayh-Dole Act is a bad law, it does have a rider that says generic production of drugs created with government funding can be mandated. However, every time patient groups have approached the NIH and asked for this provision to be enforced, as the monopoly is hurting patients who cannot afford the exorbitant prices, the NIH has rejected those requests.

For example, the U.S. Army invented a breakthrough prostate cancer drug, and Americans are paying six times the price for this drug compared to other parts of the world. But even though the government has the power to lower the price by mandating generic production, it refuses to do so.

The whole system, up and down, has been completely corrupted by the amount of money and power the industry has been allowed to amass, because of the corruption in the patent system in general,” Zaitchik says.

Big Pharma Endangers Public Health

In closing, I’d like to draw attention to a paper published in Surgical Neurology International in October 2022, titled “The Pharmaceutical Industry Is Dangerous To Health. Further Proof With COVID-19.”4

“The COVID-19 period highlights a huge problem that has been developing for decades, the control of science by industry,” the author, Fabien Deruelle, an independent researcher in France, writes.

“In the 1950s, the tobacco industry set the example, which the pharmaceutical industry followed. Since then, the latter has been regularly condemned for illegal marketing, misrepresentation of experimental results, dissimulation of information about the dangers of drugs, and considered as criminal.

Therefore, this study was conducted to show that knowledge is powerfully manipulated by harmful corporations, whose goals are: 1) financial; 2) to suppress our ability to make choices to acquire global control of public health.”

Deruelle’s paper reviews a long list of techniques that drug companies use to shape and control the science, including the following:

  1. Falsification of clinical trials and making data inaccessible
  2. Faked studies
  3. Conflict-of-interest studies
  4. Concealment of the jab’s short-term side effects
  5. Concealment of the fact there is no knowledge of the long-term effects of the COVID-19 jab
  6. Dubious composition of the COVID shots, with many ingredients remaining unlisted
  7. Inadequate testing methods
  8. Conflicts of interest within governments and international organizations
  9. Bribing of physicians
  10. Denigration of renowned scientists who express differing views
  11. The banning of alternative effective treatments
  12. Unscientific countermeasures that eviscerate liberties and freedoms
  13. Government use of behavior modification and social engineering techniques to impose isolation, masks wearing and vaccine acceptance
  14. Scientific censorship by the media

White Collar Crooks Are Running the Show

Deruelle points out that all but one of the primary drug companies producing COVID “vaccines” — Pfizer, Moderna, AstraZeneca, Merck and Johnson & Johnson — have long criminal histories, having been busted and fined huge sums for illegal marketing, recommending drugs for off-label use, misrepresenting trial results and concealing information about known dangers of their drugs. Moderna is the only exception, as it’s only been around since 2010. Deruelle writes:5

“In 2007, Merck paid $670 million, in 2009, Pfizer paid $2.3 billion, in 2010, AstraZeneca paid $520 million, and in 2012, Johnson and Johnson paid a fine of $1.1 billion …

Since 1995, Pfizer has been assessed more than $6.5 billion in penalties for 42 instances of misconduct; 36 instances of misconduct since 1995, resulting in over $11.5 billion in penalties for Johnson and Johnson; 35 instances of misconduct since 1995 and $8.8 billion in penalties for Merck.

Pfizer is singled out as having persistent criminal behavior and casual disregard for the health and well-being of patients. Pfizer is no different from other pharmaceutical companies, but it is larger and more egregious. Pfizer is a habitual offender, persistently engaging in illegal business practices, bribing physicians, and suppressing unfavorable trial results.”

Will Pfizer Stand Trial?

True to form, Pfizer is also accused of scientific fraud in its COVID-19 jab trial. Brook Jackson, who worked at one of Pfizer’s trial sites, sued Pfizer in 2021 for violating the False Claims Act.6 U.S. District Judge Michael Truncale heard oral arguments on the motions to dismiss, March 1, 2023.

As reported by The Epoch Times March 2, 2023,7 defense attorneys for Pfizer argued that “whether protocol violations occurred was ultimately irrelevant because the federal government was made aware of them but still granted emergency authorization to Pfizer’s vaccine.”

Jackson’s lawyers countered by saying the FDA authorized the vaccine before reviewing Jackson’s complaint. Judge Truncale has not issued a ruling as of this writing, and Jackson’s attorney suspects it may be weeks or even months before the judge issues his opinion.8

Conflicts of Interest Shaped COVID Responses

Deruelle also specifically delves into the conflicts of interest and relationships between the drug companies involved during COVID-19 and governments, international organizations and media — and how they worked the COVID “emergency” for their own benefit. Here are some select excerpts:9

“In 2009, the H1N1 episode should already have been enough to reveal that governments and the WHO are not autonomous. Work has shown that the 2009 H1N1 pandemic seems (based on case fatality rates [CFRs]) to have been the mildest influenza pandemic on record. Following investigations by the BMJ, it appears that this event declared by the WHO is significantly tainted by conflicts of interest.

A report by the Parliamentary Assembly of the Council of Europe has heavily criticized the WHO, national governments, and EU agencies for their handling of the swine flu pandemic: distortion of priorities of public health services all over Europe, waste of huge sums of public money, provocation of unjustified fear among Europeans, and creation of health risks through vaccines and medications which might not have been sufficiently tested before being authorized in fast-track procedures.

According to former head of health at the Council of Europe, W. Wodarg, the swine flu outbreak was a false pandemic driven by drug companies that influenced scientists and official agencies …

During the COVID-19 period, France hired private consulting firms, mainly McKinsey and Company, which is known for working with pharmaceutical companies. The Senate Inquiry Commission reports that McKinsey contributed on all aspects of the health crisis, notably for social engineering strategies on the vaccination campaign and the extension of the health pass …

The suppression of good science and scientists is not new, but COVID-19 unleashed state corruption on a grand scale, suppressing science for political and financial reasons … Since the beginning of COVID-19, much scientific data and expert opinion have been censored or labeled as false or misleading by many internet platforms …

In June 2019, the World Economic Forum (WEF) and the United Nations signed a partnership (2030 agenda). In the field of health, this alliance is designed to combat key emerging global health threats and achieve universal health coverage. In October 2019, in New York City, the Johns Hopkins Center for Health Security and its partners the WEF and the Gates Foundation, hosted Event 201, a fictional coronavirus pandemic …

Among the partners of the WEF, there are: Pfizer, AstraZeneka, Johnson and Johnson, Moderna, McKinsey, and Facebook et Google. A few months later, a coronavirus pandemic is declared, accompanied by its highly mediatized universal solution, the vaccine …

In addition to Event 201, other pandemic simulations, civil (MARS and SPARS in 2017) and military (Dark Winter in 2001, Atlantic Storm in 2003 and 2005, Global mercury in 2003, and Crimson Contagion in 2019), have taken place over the past 20 years. All these simulations correspond to fear programs induced by false media.

For the general welfare of the population, all these scenarios lead to the same methods (identical to those used during COVID-19): Isolation, control of movements and liberties, censorship, propaganda, and coercive vaccination of the population …

[T]here is no doubt that this is an event manipulated by governments, international agencies, pharmaceutical industries, and the media. In addition to the huge profits obtained by the pharmaceutical groups involved, the primary goal of this ‘pandemic’ seems to be compulsory vaccination, because the introduction of a European vaccine passport had already been planned since 2019 …

The objective of the WHO is to impose the Chinese model to become the norm. That is to say, a system with centralization of each person’s health data and restriction of freedoms for the unvaccinated … A period such as COVID-19 represents a powerful lever for increasing the effectiveness of global governance.”

Conflicts of Interest Threaten Our Freedom

In the final analysis, conflicts of interest and the collusion between government and industry does more than rob us of our hard-earned money. It now threatens our very freedom, as these monopolies are being used to further a totalitarian takeover of global proportions.

As such, we can no longer turn a blind eye or accept excuses such as “these relationships don’t influence our decision-making.” They absolutely influence the decisions being made, and the public is consistently on the losing end. Congress needs to start taking this seriously, and revisit laws such as the Bayh-Dole Act, which is currently allowing private monopolies to profit while no one is looking out for our interests.

Sources and References

And speaking of Pfizer, please see this montage of “brought to you by Pfizer.”

Remember HHS paid the media $1 Billion to peddle the COVID gene therapy injections and also paid doctors to appear in commercials. They stooped to new lows by using children in ads and calling those who got the jab “superheroes,” and that they are “helping others” by getting vaccinated.  This is pure and utter rubbish and a lie to boot.

Further, this surreal video compilation shows dozens of news anchors saying the same things verbatim, perfectly showing how mainstream media is bought out. 

More CDC Backpedaling & MMWR is a CDC Rag

http://

CDC Acknowledges Health Problems After COVID Injections

Link

Feb. 9, 2023

The Deputy Director of the CDC, Tom Shimabukuro, now acknowledges the problems of the COVID gene therapy injections.   “We hope these people improve.” Can you believe this? What is the recourse for injured families?

Other experts are also speaking out:

  • MIT professor Dr. Levy took to Twitter to share the harm the shots are causing
  • Israeli health reporter Yaffa Shir-Raz stated that “Israel was Pfizer’s laboratory” and that Israel did not have any functioning monitoring system, yet the FDA’s decision to approve the booster shot was based on Israeli data
  • Dr. Masanori Fukushima slammed Japan’s Ministry of Health for refusing to halt the COVID injection program, citing data which shows a multitude of adverse reactions and deaths
  • Professor Masanaka Nagao, Forensic Medical Dotor from Hiroshima University School of Medicine states that data shows ‘vaccination’ was sufficiently related to immune abnormalities
  • Professor Shigetoshi Sano, expert in dermatology, from Kochi University of Medicine used a special dye to examine tissues of the “vaccine” injured and found inflammatory areas flooded with spike proteins from the injections
  • Joseph Fraiman, an emergency physician and a clinical scientist from Louisiana who reanalyzed Pfizer and Moderna Trials found that the “vaccines” increase serious adverse events at a rate of 1 in 800 and calls for them to be withdrawn from the market
  • Dr. Ryan Cole, pathologist and CEO and medical director of Cole Diagnostics states that the spike protein is a toxin that is being injected into everyone that crossed the blood, brain, barrier and causes damage in organs
  • Dr. Hoffe has used D-dimer tests on the “vaccinated” and found microclotting causing capillaries to plug up
  • Dr. Sucharit Bhakdi, world renowned virologist and professor states the “vaccines” are injuring and killing untold numbers of people globally & must be stopped
  • Dr. Flavio Cadegiani, Brazilian endocrinologist states the spike protein in the shots induces disease in the endocrine system

But I was greatly encouraged after seeing the cringe-worthy video of Fauci, 82, and the Democratic mayor making the rounds in the Anacostia neighborhood in June 2021 attempting to peddle the clot shots.  Many truth bombs were shared by ordinary citizens who famously stood their ground.

http://  Approx. 11 Min

Link

March, 2023

Waffling Walensky

In this video, Vinay Prasad, discusses CDC Director, Rochelle Walensky’s ever changing statements.  He also wrote a Substack article titled: Public Health Should Lose Your Trust.  This important article breaks down the COVID issues and why public health failed, utterly.  He also wrote this enlightening article titled Mask Studies Reach a New Scientific Low Point.

I had to chuckle when I read:

Enter a new study in MMWR— the CDC’s pet journal; It is getting widely tweeted and cited, and that is unfortunate. The paper is entirely, irredeemably flawed. Its flaws are so evident that it should not have been published nor promoted. When an issue is deeply polarizing, publishing bad science helps no one. It cannot convince skeptics, proponents don’t need convincing, and it deepens mistrust in institutions. Let’s consider the paper.

I chuckle because the MMWR has been used to spank Lyme/MSIDS patients as well:   https://madisonarealymesupportgroup.com/2017/06/23/no-bias-in-mmwr-for-any-other-infectious-disease-requiring-iv-antibiotics-except-for-lyme/

Hopefully by now you have realized that the CDC is an entirely political organization that has very little to do with science or public health.

An interesting little tidbit about the MMWR is that while it has the look and feel of articles in medical journals, its published content constitutes the official voice of its parent, the CDC.  Most MMWR articles are not “peer-reviewed” in the way submissions to medical journals are.  The content in the MMWR agrees with CDC policy and every submission undergoes a rigorous multilevel clearance process, including a review by the CDC Director before publication..  By the time a report appears in the MMWR, it reflects or is completely consistent with CDC policy.  Dissenting opinions simply will not be published.

Interestingly, the CDC did a similar mask study in 2020 and found a near-perfect lack of correlation so they simply buried the results in a table they ignored in the actual text of the MMWR.

Another particularly poignant quote:

The truth is the CDC has put out so many papers that borderline propaganda, that they create the space for people to seek alternative information. They have lost trust.

Ultimately, the CDC & NIH failed us. The agencies should have run a half dozen masking cluster RCTs under different conditions, and for different ages. We were starving, and we needed this loaf of bread. Instead, the CDC published flawed study after flawed study. It didn’t even give us crumbs; it gave us a fistful of sand. Starving, we swallowed each grain, and begged for more. Medical leaders told us to fill our bowl before it runs out. Science lies on its deathbed. ~ Dr. Vinay Prasad

Well, at least the CDC isn’t alone.

Germany’s Minister of Health Karl Lauterbach, who once claimed that COVID-19 “vaccination” is free of side effects, admitted last week that he was wrong, saying adverse reactions occur at a rate of one in 10,000 doses and can cause “severe disabilities.”  Unfortunately, a scientist has reviewed both the Pfizer and Moderna trial data and found it’s far worse.  According to this data, it’s actually one serious adverse event per 800 vaccinees.

The CDC is beyond hope and rehabilitation and is so corrupt it has forgotten what truth even sounds like.

Until the Bayh-Dole Act and other measures are repealed, we will never be able to trust public health due to their severe conflicts of interest.

For more:

For fantastic resources on all things vaccine:

Report Linking Fluoride to Lower IQ in Children Made Public After CDC, HHS Tried to Block It

https://childrenshealthdefense.org/defender/ntp-report-fluoride-lower-iq-children

Report Linking Fluoride to Lower IQ in Children Made Public After CDC, HHS Tried to Block It

The National Toxicology Program on Wednesday released a draft report linking prenatal and childhood fluoride exposure to reduced IQ in children, after public health officials tried for almost a year to block its publication.

The National Toxicology Program (NTP) on Wednesday released a draft report linking prenatal and childhood fluoride exposure to reduced IQ in children, after public health officials tried for almost a year to block its publication.

The U.S. Department of Health and Human Services (HHS) and the Centers for Disease Control and Prevention (CDC) initially blocked the NTP from releasing the report, according to emails obtained via a Freedom of Information Act (FOIA) request.

But a court order stemming from a lawsuit filed by Food and Water Watch against the U.S. Environmental Protection Agency (EPA) forced the report’s release this week.

The NTP, an interagency program run by HHS that researches and reports on environmental toxins, conducted a six-year systematic review to assess scientific studies on fluoride exposure and potential neurodevelopmental and cognitive health effects in humans.

The report, containing a monograph and a meta-analysis, went through two rounds of peer review by the National Academies of Sciences, Engineering, and Medicine. Comments from reviewers and HHS and NTP’s responses also were included in the report released Wednesday.

According to its website, the NTP “removed the hazardous classification of fluoride” in response to comments in the peer-review process. Yet, the report states:

“Our meta-analysis confirms results of previous meta-analyses and extends them by including newer, more precise studies with individual-level exposure measures.

“The data support a consistent inverse association between fluoride exposure and children’s IQ

“The results were robust to stratifications by risk of bias, gender, age group, outcome assessment, study location, exposure timing, and exposure type (including both drinking water and urinary fluoride).”

“These findings fly in the face of the empty, unscientific claims U.S. health officials have propagated for years, namely that water fluoridation is safe and beneficial,” said Robert F. Kennedy, Jr., Children’s Health Defense chairman and chief litigation counsel. “It’s past time to eliminate this neurotoxin from our water supply.”

The controversial report will play a key role in determining the outcome of a lawsuit brought in 2017 by several nonprofits against the EPA to end fluoridation of drinking water, plaintiffs’ attorney Michael Connett told The Defender.

We had to fight hard to have this report even made public,” Connett said. “They [CDC and HHS] buried this. If they had gotten their way, this report would have never even seen the light of day,” Connett said.

Since the trial began in 2020, U.S. District Judge Edward Chen has been waiting for the NTP to complete a systematic review of fluoride’s neurotoxicity before ruling on the case.

Groups like the American Dental Association publicly pressured the NTP to “exclude any neurotoxin claims” from the reports.

Connett said during the trial, the EPA repeatedly claimed that the plaintiffs’ allegations about toxicity could not be verified because there was no “systematic review.”

The documents released Wednesday fill that gap.

Connett said:

“So now what do we have? We have a systematic review by one of the pioneering, leading, most authoritative research groups on toxicology in the world.

“They just completed a systematic review that took them six years to complete, so if that’s not enough to demonstrate a hazard under the toxic substances control act, then how would any citizen group ever be able to meet the standard?”

The findings: fluoride and lowered IQ in children

According to the NTP report:

“The current bodies of experimental animal studies and human mechanistic evidence do not provide clarity on the association between fluoride exposure and cognitive or neurodevelopmental human health effects.”

Yet, the report’s summary contradicts this statement by summarizing the evidence informing this conclusion, stating that nearly all studies examined for this literature review found evidence of cognitive or developmental issues associated with fluoride.

According to the report, 8 of the 9 “high-quality studies examining cognitive or neurodevelopmental outcomes reported associations with fluoride exposure.”

Of the 19 high-quality studies assessing the association between fluoride and IQ in children, 18 reported an association between higher fluoride exposure and lower IQ in children. Forty-six of the 53 low-quality studies also found evidence of that association.

The meta-analysis also states:

“The body of evidence from studies on adults is also limited and provides low confidence that fluoride exposure is associated with adverse effects on adult cognition. There is, however, a large body of evidence on IQ effects in children.”

The monograph and meta-analysis found that fluoride exposure at levels equivalent to 1.5 mg/L is associated with lower IQ in children. The abstract concludes:

“This review finds, with moderate confidence, that higher fluoride exposure (e.g., represented by populations whose total fluoride exposure approximates or exceeds the World Health Organization Guidelines for Drinking-water Quality of 1.5 mg/L of fluoride) is consistently associated with lower IQ in children.”

Levels of fluoride found in drinking water in the U.S. are typically 0.7 mg/L, which is lower than the 1.5 mg/L levels found to be neurotoxic by the reports.

On that basis, HHS’ review of the reports recommended the NTP revise its assessment such that, “all conclusory statements in this document should be explicit that any findings from the included studies only apply to water fluoride concentrations above 1.5 mg/L.”

The NTP responded:

“We do not agree with this comment. Our assessment considers fluoride exposures from all sources, not just water.

As discussed in the pre-publication 2022 NTP Monograph, because fluoride is also found in certain foods, dental products, some pharmaceuticals, and other sources, individual behaviors are likely an important determinant of actual exposures.

Rick North, former CEO of the American Cancer Society’s Oregon division and Fluoride Action Network board member told The Defender that “people consume large amounts of fluoride through tea and other drinks and processed foods made with fluoridated water, not to mention pesticide ingestion and fluoride from air pollution.”

He also said that people’s fluoride exposure can depend on how much water they drink.

“Think about it,” North said. “Your level of risk depends upon, incredibly, how thirsty you are. That’s how absurd the entire premise of water fluoridation is,” he said.

The NTP confirmed that people exposed to levels of fluoride lower than 1.5 mg/L in the water system could have high levels of fluoride in their systems. It stated:

“Even in the optimally fluoridated cities [fluoridated at 0.7 mg/L] in Canada studied by Green et al. (2019), individual exposure levels, as documented by repeated urinary measurements, suggest widely varying total exposures from water combined with fluoride from other sources.”

It added, “our moderate confidence conclusion is primarily based on studies with total fluoride exposure that approximates or exceeds what is generally associated with consumption of optimally fluoridated water [0.7 mg/L] in the United States.”

“We have stressed in our monograph that our conclusions apply to total fluoride exposures rather than to exposures exclusively through drinking water.”

“What the NTP is pointing to here is that in some communities, where the dose of fluoride in the water is 0.7 mg/L, the NTP has found levels of fluoride found to be associated with lower IQ,” Connett told The Defender.

Also, different people have different risk levels, he said. Pregnant women and bottle-fed babies, for example, are some of the populations at highest risk.

On this point, the NTP responded to a different HHS critique, writing, “We have no basis on which to state that our findings are not relevant to some children or pregnant people in the United States.”

“The margin of safety here just doesn’t exist — it is precariously small,” Connett said. He added that the lawsuit is “basically a risk assessment of fluoride.”

Under the Toxic Substances Control Act (TSCA), which is the law at stake in the lawsuit, the EPA carries out risk assessments for potential toxins.

To do a risk assessment, the EPA first identifies a hazard and determines at what dose — what level of human exposure — that hazard harms human health.

Then the agency determines in a given case whether the margin between the existing hazard levels and the human exposure levels is unacceptably close, which would make a toxin pose a risk to human health.

Connett said that in EPA’s previous risk assessments for other chemicals, such as methylene chloride or bromopropane, evaluated according to the 2020 risk evaluation method that guides this case, the agency found the hazard level exceeds the human exposure level by much higher margins — “usually in a range of ten to 20 times higher,” yet it has deemed those chemicals to present an unreasonable risk to human health.

In other words, the substances were found to be toxic to humans at levels significantly lower than what people may be exposed to in regular use, yet the EPA determined them to be risks.

When it makes that determination, the EPA must then take steps to mitigate the risk.

That can also be the finding in this case. According to a pre-trial document, both sides in the case agreed to the “undisputed fact” that the “EPA does not require that human exposure levels exceed a known adverse effect level to make an unreasonable risk determination under TSCA.”

The NTP documents also raised flags about the implications of seemingly small neurotoxic effects:

“Research on other neurotoxicants has shown that subtle shifts in IQ at the population level can have a profound impact on the number of people who fall within the high and low ranges of the population’s IQ distribution.

“For example, a 5-point decrease in a population’s IQ would nearly double the number of people classified as intellectually disabled.”

Top HHS and CDC officials tried to ‘water down’ and block the report

In 2016, a group of six nonprofit organizations and several individuals petitioned the EPA to end fluoridation of drinking water in the U.S. based on evidence of health risks associated with fluoride, namely neurotoxicity.

The EPA rejected the petition.

In response, Food and Water Watch, Fluoride Action Network and others sued the EPA in 2017, seeking an end to water fluoridation.

The plaintiffs argued that water fluoridation violates the EPA’s Toxic Substances Control Act and that fluoride is neurotoxic and lowers children’s IQ.

They based their initial claims on dozens of studies and reviews demonstrating fluoride’s neurotoxicity. Studies have also linked fluoride to a variety of other health risks in both children and adults, and evidence shows it to be an endocrine disruptor.

The EPA denied water fluoridation causes harm.

A seven-day trial took place in federal court in San Francisco in June 2020, but Judge Chen put the proceedings on hold pending the release of NTP’s systematic review of research available on the neurotoxic effects of fluoride.

The report, slated for release in May 2022, was delayed several times and sent for several rounds of peer review.

“The people on the [NTP] committee were experts in their fields who put years into this study, going back and forth with one external review after another,” North said. “You couldn’t ask for more peer review than what it already had. There were constant attempts to delay it, to water it down.”

In late October 2022, Judge Chen ended the stay on the NTP review, ruling that the parties involved could view the NTP review in its unpublished form to better inform his final decision.

However, due to concerns from the EPA, he also ruled the report could not be made public unless the NTP released it.

In December 2022, the plaintiffs filed several exhibits with Judge Chen, including a redacted version of the NTP’s assessment of fluoride’s neurotoxicity and internal emails between the CDC and the NTP obtained through FOIA demonstrating that HHS blocked the release of the long-delayed review, the plaintiffs argued.

The documents showed that on May 11, NTP notified the agencies that it was going to release the report on May 18, but the CDC opposed the release.

Emails also indicated that HHS Assistant Secretary for Health Rachel Levine was going to “get involved,” and, “the May 18 release date for [the monograph] is almost certainly not going to happen,” the Defender reported.

Connett said:

It was only because we were tipped off by someone with knowledge on the inside that something was amiss that we went and did extensive FOIA requests and we were able to get documents showing that the NTP scientists considered this report to be complete and ready for publication last May, May of 2022.”

North said it was clear the agencies were blocking the release of the report, which was ready for publication.

“This was a clear case of stonewalling,” North said. “The National Toxicology Program, after over six years of research and numerous outside peer reviews, had completed its state-of-the-science report.”

Connett added:

“We have emails showing that Levine is the one who put it on hold. Rachel Levine said not to publish this report at this time. Then we got the FOIA emails showing that and NTP said they may not publish this [the report] at all. They may not publish it in final form but we did get them to agree to at least post a draft report. They will consider it a draft report.”

On January 20, Judge Chen denied the EPA’s request to add another six-month period to the stay he lifted in his October ruling.

The monograph and meta-analysis released yesterday on the NTP’s website are both labeled “draft.”

“Unfortunately, fluoridation promoters and high-level government officials have continued to label it a draft,” North said. “It wasn’t.

Experts associated with the lawsuit against the EPA will now analyze and interpret the report in future hearings and then Judge Chen will rule.

The next hearing date is scheduled for April 11, 2023. At that time, the judge will set a date for the next phase of the trial.

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

For more: