Archive for the ‘Activism’ Category

Doctored Images, Fake Data, & Plagiarism: Scandals Rock Alzheimer’s & Cancer Research. Research Director Falsifying Vaccine Data Retains Post

In another update, Southwest National Primate Research Center (SNPRC) is allowing one if its directors who published fraudulent research on tuberculosis vaccines to retain his post, according to Science.org

“[Deepak Kaushal] engaged in research misconduct by intentionally, knowingly, and/or recklessly falsifying and fabricating the experimental methodology to demonstrate results obtained under different experimental conditions,” according to ORI findings published in the Federal Register on Monday.

The ORI’s investigation found that Kaushal “engaged in research misconduct” involving one published study and two grant applications under at least eight U.S. government grants from the Institute of Allergy and Infectious Diseases (NIAID) and National Institutes of Health (NIH).   

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**UPDATE Aug. 2022**

http://    Approx. 20 Min

Aug. 3, 2022

Another Major Blow to Science, Trust, the FDA, and Peer-Review

By Chris Martenson

Go here if Youtube censors the video.

And here for another video on “Bad Science: Breaking Our Public Trust”

https://www.medpagetoday.com/special-reports/features/99918?

Doctored Images in Alzheimer’s Research?

By Sophie Putka

July 27, 2022

Excerpts:

An investigation by Science Magazine tells how Matthew Schrag, MD, PhD, neuroscientist and physician at Vanderbilt, unearthed serious problems with research on a protein subtype of amyloid beta that has been a cornerstone of research and spending on Alzheimer’s for over a decade.

Schrag found that images accompanying highly cited Alzheimer’s studies touting major breakthroughs for the field were very plausibly altered. Using the online platform PubPeer, where scientists flag mistakes in research, Schrag stumbled upon comments on articles led by Sylvain Lesné, PhD, of the University of Minnesota.

One of the papers, published in Nature, has been cited 2,300 times, and related NIH funding for related oligomer and Alzheimer’s research grew to $287 million. Lesné and the lab where he worked won accolades: awards, grants, and prominence. “You can cheat to get a paper. You can cheat to get a degree. You can cheat to get a grant. You can’t cheat to cure a disease,” Schrag told Science Magazine. “Biology doesn’t care.”

(See link for article)

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SUMMARY:

  • Nature has learned that formal investigations finding multiple instances of research misconduct including data falsification and plagiarism have been made against superstar cancer researcher Carlo Croce, MD and scientists under him.
  • So far nobody is admitting fault, and in fact Croce is suing the university despite the committee saying he was a poor mentor and the lab lacked oversight.  Further, the university instructed Croce and his team to retract or correct more than a dozen papers but only one has been retracted and two corrected.
  • Biotronick, a medical device manufacturer, paid and rewarded docs to use their implantable heart devices and violated the False Claims Act when they submitted reimbursement claims for the related procedures from Medicare and Medicaid, according to the DOJ.  The company paid for training that never occurred, as well as holiday parties, winery tours, lavish meals, international business class airfare and honoraria with no legitimate business purpose.

Hopefully, it is becoming clearer by the day that science has been completely hijacked.  It was recently discovered that $350 Million in secret payments have been given to Fauci, Collins, and other NIH scientists.  Corruption in public health has been exposed beautifully thanks to COVID, but is certainly not new.  Lymeland has been riddled with corruption for over 40 years. There is an urgent need to break the public health monopoly which is literally getting away with murder.

The CARES Act, provides hospitals with bonus incentive payments for all things related to COVID-19 (testing, diagnosing, admitting to hospital, use of remdesivir and ventilators, reporting COVID-19 deaths, and vaccinations) and waivers of customary and long-standing patient rights by the Centers for Medicare and Medicaid Services (CMS) are the reasons patients are virtual prisoners in the hospital.  They have no choice, no say, and are barbarically isolated from family members. They are only allowed “FDA approved” COVID treatments which are dangerous, ineffective, and expensive.

Time for a CDC/NIAID FDA/ walkaway movement.

For more:

Category:

Activism, research

COVID Shot Testimonies & CDC Can’t Hide This Anymore: Leaked Emails. Is This Why Fauci’s Retiring?

https://odysee.com/@Commentator:e4/video_2022-03-16_13-10-03:9?src=embed

Approx. 1 hour 40 min

MRNA ‘VACCINE’ GENOCIDE 2021-2022: TESTIMONIES FROM THE VICTIMS AND MEDICAL STAFF

Hear the voices you will not hear on mainstream media.

http://  Approx. 21 Min

Aug. 1, 2022

CDC Can’t Hide This Anymore – Leaked Emails

The CDC is refusing to hand over data about vaccine trials and possible adverse affects, despite a request for this information. Also, new emails show that the CDC worked in lockstep with social media companies to help shut down any conversation around vaccines that they did not like.  It’s clear Big Tech has colluded with the federal government to censor, silence, and suppress free speech.

Internal communications obtained and shared by America First Legal (AFL) show that the CDC had consistent contact with officials from corporate social media companies to address the spread of “misinformation.” AFL received the documents after filing a Freedom Of Information Act (FOIA) request with the CDC and a lawsuit to expedite the process.

The documents show personal communications between Carol Crawford, the Digital Media Branch Chief for the CDC, and representatives of Google, Facebook, and Twitter.

The emails show that Facebook gave the CDC and the Department of Health and Human Services (HHS) over $15 million in free advertising on the platform, described as a “non-monetary gift.”  Source

“CDC and social media worked hand-in-glove propagandizing the false narrative:

  1. Masks work
  2. They are “safe and effective”  (The COVID injections)
  3. They reduce the risk of hospitalization and death (the injections)
  4. They “protect others” i.e. reduce spread (the injections)

Dr. Peter McDullough

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July 18 (Reuters) – Dr. Anthony Fauci, the chief medical adviser to the White House, confirmed he will retire by the end of President Joe Biden’s first term, but it could come much earlier than that, the infectious disease expert told Reuters in an interview on Monday.

For more on Fauci:

For more on COVID injections:

Category:

Activism, vaccines, Viruses

The Bear Metaphor & Your DNA

https://naomiwolf.substack.com/p/facing-the-beast

Facing the Beast

Can We Really Confront the Biggest Crime in Human History?

Dr Naomi Wolf
Excerpts:

I was relaxing in our screened porch in our little cottage in the forest, feeling rather pleased with myself. It had been an arduous week of the usual combat for liberty, but there had been victories.

Then I heard a “thump” about eight feet away behind my head.

I glanced behind me and saw the enormous ears and forehead of a sizable brown bear, who was ducking insolently, clearly aware of me, to lower himself behind the trash cans.

My heart pounded as I realized that he was not leaving; he continued pacing and circling, no matter where I went.

He was here because — I had done nothing to stop him. He was here because I let him slowly take over our home.

This all, of course, really happened. But that does not mean it is not also a metaphor.

The same week that this happened, I also finalized my reporting about the Pfizer vaccines, showing — what I knew for months I would eventually find.

The heart of the manufacture and distribution of millions of doses of the MRNA vaccines that are causing such a swath of death and destruction throughout North America and Western Europe, is enmeshed with the plans, methods and manufacturing infrastructure of our existential adversary.

The enemy is within our very bodies.

(See link for article)

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SUMMARY:

  • Wolf believes this isn’t just about a greedy pharmaceutical company and a corrupt regulatory agency but a massive act of war.
    • Doubling of neonatal deaths, 34% above normal stillbirths and spontaneous abortions for “vaxxed” moms
    • 40% increase in death rates, shocking rise in disability
  • 2021 Hong Kong study (answerable to the CCP) showed when mice got the second dose of the booster, it resulted in visibly enlarged hearts with white patches, cytokine storms and liver damage seen by the naked eye.  The study concluded: “Post-vaccination myopericarditis is reported after immunization with coronavirus disease 2019 (COVID-19) messenger RNA (mRNA) vaccines.” 

  • Pfizer/BioNTech is a German-Chinese company and has an MOU with Fosun Pharmaceuticals, a major CCP-linked pharmaceutical company based in Shanghai, to make the Pfizer/BioNTech MRNA “vaccines”.  A SEC filing shows that the MOU with Fosun includes an equity investment by Fosun in BioNTech. In other words, the CCP is an equity investor in BioNTech.  Fosun is not separate from the CCP; it is the CCP.
  • Fosun Pharma did not stay in China.  It came here. Fosun Pharmaceuticals is now also Fosun Pharmaceuticals USA, with branches for R and D and product formulation in Boston, MA and Princeton, NJ.
    • Fosun produces products in the US for distribution here and around the world and has has built a “global operation strategy” for the manufacture of COVID-19 vaccines, COVID-19 PCR tests and COVID-19 antigen tests. (These tests were the primary metric that determined the ‘pandemic’ and thus the lock downs. So a CCP-run company, and a CCP product decides who can go to work, school, and travel.)
    • A lawsuit has been filed in NY surrounding COVID testing because commercial labs get DNA, which then goes to Fulgent Genetics, which states they’re going to destroy all the samples and that they aren’t selling them to 3rd parties.
      • But a House Intel Committee Member warns that DNA test kits could lead to targeted bioweapons.
      • The LA County Sheriff’s Department announced they will not work with a China-linked genetics firm hired by the county to conduct COVID testing and registration because the FBI shared “very concerning information” about Fulgent Genetics Corporation – which was awarded a no-bid contract for the work.  LASD states DNA data from COVID testing is not guaranteed to be safe and secure from foreign governments and “will likely be shared with the Republic of China.”
        • China just happens to be quietly building the worlds largest DNA database.  All those COVID tests results will come in handy.
        • The FBI is shocked to find that China’s offer to build $100 Million ‘garden’ in DC just might be for espionage purposes.
        • There is growing concern over Chinese interests purchasing large swaths of land, particularly farmland, in the U.S. – including one sensitive parcel in North Dakota in the proximity of a military installation.
        • While Americans are paying $5 per gallon of gas, DOE docs show the Biden admin has sold nearly 6 million barrels of oil from the U.S. strategic reserve to an entity tied the CCP (Sinopec, parent org of Unipec through BHR Partners), which in turn has ties to Hunter Biden. The Biden admin. has also shipped more natural gas to Europe than promised.
    • Fosun obtained the Medicines Patent Pool (MPP)’s license to produce and supply the generic versions of:
      • Merck’s oral COVID-19 treatment Molnupiravir 
      • Pfizer’s oral COVID-19 treatment Nirmatrelvir
      • Pfizer’s Nirmatrelvir and Ritonavir
    • Fosun, a CCP-owned hybrid entity is making millions off of Pfizer injections, Monupiravir, and Paxlovid, so when Biden does a deal with Pfizer with our tax dollars, and gets billions in omnibus bills for PPE, including millions for PCR and antigen tests, he is writing checks to China.
    • A 2018 whistleblower broke a scandal revealing that Fosun Pharmaceuticals had “massively” faked its data and bribed regulators. The FDA wrote them a stern letter.

Important quote:

So take all of the above, and map it against the 150,000 plus adverse events in the Pfizer documents, the deadly harms to reproduction, the Western baby die-off, the babies in seizures; map it against the population drop, the rise in disabilities, map it against the rigid, cruel vaccine mandates aimed at Western defense forces (Canada’s, and Australia’s and all of Western Europe’s, as well as at the most powerful military in the world, that of the United States) — map it against the vaccine mandates aimed at our police, our health care workers, our firefighters, our pilots, our first responders, our kids, our babies — all this done by a White House captive, via Hunter Biden’s laptop, to the CCP.

This all means, of course, that we are staring into the abyss right now.

Traumatized or not, we all need to snap out of denial.

We let our adversary come too close to us. Into our very bloodstreams.

We need to save each other.

We need to turn and face the ravening beast.

Category:

Activism, Testing, vaccines, Viruses

Public Health Vaccine & Treatment Fraud

https://popularrationalism.substack.com/p/how-fauci-and-grady-lowered-the-standards

How Fauci and Grady Degraded the Standards of Ethical Requirements for Clinical Research in the US Compared to the Rest of the World

In reading Nuremberg, The Belmont Report, and now the Helsinki Declaration, I can say that up to 2020, US had far lower ethical standards for human subjects research than WMA. Now? None.

James Lyons-Weiler
Excerpts:

Both WHO and the US HHS suffer from a form of ethical blindness when it comes to vaccine research. Foregoing long-term vaccine safety studies in favor of retrospective analysis of real-world data, these agencies fail to recognize that post-marketing (and post-EUA) studies are de facto uncontrolled, non-randomized prospective clinical trials conducted without proper consenting procedures.

If you’ve read the Nuremberg Code, the Belmont Report, and the Declaration of Helsinki, you’d know that protections are supposed to be in place not for some people undergoing some clinical studies, but instead are considered to be required to be in place for all people undergoing any clinical studies.

Where the US had departed (prior to 2020) from the rest of the countries that backed Helsinki (WMA) and participated in its updates included, according to Kimmelman et al. (2009) included:

  • Disclosure of conflict of interest
  • Public disclosure of study design
  • Benefit for populations in which research is conducted (beneficence)
  • Reporting of accurate results and publication of negative findings
  • Access to treatment after research has been conducted
  • Restriction of use of placebo in a control group where effective alternative treatment is available

The departure formally came when issues related to HIV clinical trials run in less wealthy countries seemed to depart from Helsinki standards. Rather than work to reconcile differences with Helsinki, US companies, and the US government came up with a different international standard called “Good clinical practice” – standards in place in the EU (codified as Directive 2001/20/EC), and the US (enforced as policy by NIH), all backed by Pharma.

The departure of the US and the EU from the countries that continue to abide by Helsinki serves to empower those running clinical trials at the expense of those individuals taking on the risk of new drugs and vaccines – both in the risk of poor efficacy and in the risk of potential safety issues.

Well, it turns out that Fauci was at the forefront of the war on ethical research, arguing against the requirement of the use of placebos in HIV drug trials in Africa.

Fauci’s insistence on no placebo arm in HIV drug trials in Africa is an example of bluster and posturing on morality to hide the negative consequences (harm) of the drug AZT. We’ve seen this bluster and posturing all along with COVID-19 vaccines, and Fauci’s denial of the efficacy of early treatment. He rolls over so many of the principles of medical research ethics – and ethics of care – those that were meant to be sacrosanct to protect the interests and well-being of individuals, as outlined in Nuremberg, Helsinki, and the Belmont Report.

Medical hubris has been the modus operandi of Fauci well before COVID-19.

It’s time to revisit why and how it came about that the pharmaceutical companies are able to write the rules by which they conduct clinical research.

(See link for article)

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Please see Jeremy R. Hammond’s antidote to government and mainstream media’s disinformation:

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https://childrenshealthdefense.org/defender/fda-moderna-bypass-covid-vaccine-safety-standards-documents/

FDA Colluded With Moderna to Bypass COVID Vaccine Safety Standards, Documents Reveal

According to Alexandra Latypova, an ex-pharmaceutical industry executive, documents obtained from the U.S. Department of Health and Human Services on Moderna’s COVID-19 vaccine suggest the U.S. Food and Drug Administration and Moderna colluded to bypass regulatory and scientific standards used to ensure products are safe.

fda moderna covid vaccine safety

Excerpts:

After analyzing 699 pages of studies and test results “supposedly used by the FDA to clear Moderna’s mRNA platform-based mRNA-1273, or Spikevax,” Latypova told The Defender she believes U.S. health agencies are lying to the public on behalf of vaccine manufacturers.

“It is evident that the FDA and NIH [National Institutes of Health] colluded with Moderna to subvert the regulatory and scientific standards of drug safety testing,” Latypova said.

“They accepted fraudulent test designs, substitutions of test articles, glaring omissions and whitewashing of serious signs of health damage by the product, then lied to the public on behalf of the manufacturers.”

(See link for article)

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https://childrenshealthdefense.org/defender/biden-pharma-fda-officials-covid-booster-timeline

Biden, Pharma Pressured Top FDA Officials to Approve Booster Timeline, Emails Reveal

Judicial Watch today announced it received 112 pages from the U.S. Food and Drug Administration that show top officials being pressured by “companies and for that matter the administration, who try to impose timelines [sic] that make no sense.”

Excerpts:

The records were produced to Judicial Watch in response to a February Freedom of Information Act (FOIA) lawsuit against the Department of Health & Human Services (HHS) that was filed after HHS failed to respond to a Sept. 3, 2021, FOIA request for records of communication from the former director and deputy director of the FDA’s Office of Vaccines Research and Review, Dr. Marion Gruber and Dr. Philip Krause, respectively (Judicial Watch v. U.S. Department of Health and Human Services (No. 1:22-cv-00292)).

Drs. Gruber and Krause reportedly resigned during the White House’s push to approve the COVID-19 vaccine “booster shots.”

(See link for article)

The FOIA requests and lawsuits uncover a substantial amount of info on many COVID issues including a FBI inquiry, NIAD’s money and grants to EcoHealth Alliance and Wuhan for bat coronavirus research, Fauci emails citing ties between Wuhan and EcoHealth, Gates’ involvement with the Chinese government, HHS records showing a grant application for “gain of function” research on bat RNA, viruses, and genetic manipulation of SARSr-CoV WIV1 strain, HHS records showing the Pfizer lipid nanoparticles were found in the liver, adrenal glands, spleen, and ovaries of test animals 8-48 hours after injection, safety lapses at U.S. biosafety labs, and HHS records showing NIH officials tailored confidentiality forms to China’s terms.

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HFDF ANNOUNCES LEGAL ACTIONS IN PARTNERSHIP WITH DAILYCLOUT

Leslie Manookian, HFDF President, has partnered with Dr. Naomi Wolf, DailyClout CEO, to hold the FDA accountable for its unscrupulous and unlawful approval of remdesivir for all patients, and COVID injections for young children.

Category:

Activism, Treatment, vaccines

We Should Not Have to Fight So Hard For Lyme Care

https://www.lymedisease.org/monica-white-wg-comments/

To TBDWG: We should not have to fight so hard for Lyme care

Monica White's comments to TBD Working Group

Monica White delivered the following public comments to the Tick-Borne Disease Working Group on July 19.

My name is Monica White. I’m president/co-founder of Colorado Tick-Borne Disease Awareness Association. I’ve lived with chronic Lyme, co-infections and conditions for nearly 16 years, due to lack of an early diagnosis and treatment.

Formerly a fully functional wildlife biologist and wildland firefighter for the US Forest Service, I am functional now only with repeated courses of combined antibiotics, antimicrobial, and immune therapies.

I recently relapsed with tick-borne illness after a period of no treatment. And again, even with current positive lab results in hand, I was met with dismissal from mainstream medicine.

When I had an enlarged liver and spleen during another extended hospital stay, the infectious disease doctor wrote in my report–and I quote–“I highly doubt this is in anyway related to either Lyme disease or babesiosis.”

I again left hospital care without a diagnosis. And I’ve again made improvements in my health only with re-treatment for tick-borne diseases. This dismissal of TBDs in the differential diagnosis is commonplace for TBD patients, especially those with chronic or persistent disease.

Though persistence of pathogens is shown in multiple studies conducted by respected researchers in the community, some on this panel–and is found in both animals and humans–findings have thus far been ignored or disputed by many members of this panel each year. It is past time to settle the science on this issue for:

  • patients that don’t get early accurate diagnosis and treatment.
  • patients that fail short course single antibiotic/antimicrobial therapies;
  • patients that are overlooked for have co-infections or tick-borne conditions,
  • and patients that do not respond to currently available therapies.

Maternal-fetal transmission

Maternal-fetal transmission of many TBDs is a fact, but research is lacking in diagnostics and treatment before irreparable damage has occurred. My own children acquired Lyme and co-infections congenitally, and both suffered from delayed diagnosis and treatment, as well as from multiple relapses of disease.

The resources available to patients have been… and continue to be…. INADEQUATE. Our medical system is failing these patients. This has ramifications that go so far beyond my individual story.

We should not have to fight as hard as we have… for as long as we have…to get government funded reliable direct diagnostics and curative treatments for acute and persistent disease!

Individuals…families…OUR children have been losing EVERYTHING for DECADES due to the lack of attention to the seriousness and the debilitation that Lyme, other TBDs and conditions have on those infected or exposed.

There is no excuse for patients having to spend months, years, or decades seeking accurate diagnosis and treatment, with crippling physical health, mental health, financial burdens, loss of careers, and relationship stresses beyond what many families can endure.

No one should suffer the way I have suffered…the way my children have suffered… and the way that the patients I share a voice for…have suffered.

Patient’s needs MUST be the priority of the Working Group for this final phase of the panel!

Thank you.

In addition to co-founding the Colorado Tick-Borne Disease Awareness Association, Monica White has served on a subcommittee of the federal Tick-Borne Disease Working Group, and on other governmental panels.

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**Comment**

Fighting “hard” isn’t nearly as important as fighting “smart,” and the Lyme/MSIDS community continues to work with the very people and organizations behind the corruption, denial, and fraud.

Time to support independent scientists who are not being gagged and who are not biased and part of the machine.

Category:

Activism, Lyme