Author Archive

Paxlovid Rebound Strikes Again

http://

The Kim Iversen Show

Aug. 1, 2022

Biden Pushes More Pills and Shots Despite Rebounds

There’s no data on Paxlovid on those who have had COVID shots.  Fauci also suffered a rebound case, which was worse than his first go around.

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https://www.medpagetoday.com/opinion/second-opinions

What’s Really Driving COVID ‘Rebound’ After Paxlovid?

— There’s only one way to find out

by Daniel A. Sweeney, MD, Cameron R. Wolfe, MBBS, MPH, and Andre C. Kalil, MD, MPH August 2, 2022

A photo of the packaging and blisterpack of Paxlovid.

In the early days of the pandemic there was an understandable rush to define and optimally treat COVID-19. Anecdotal evidence and the opinions of eminent scientists and non-scientists overwhelmed social and mainstream media platforms only to eventually be overruled by the results of careful, scientific analyses and well-designed clinical trials. Now, more than 2 years into the pandemic, we must return to the standard of careful and thorough analyses for all interventions and treatments.

The debate about “COVID-19 rebound” after nirmatrelvir/ritonavir (Paxlovid) treatment is one of these timely areas warranting further investigation. Continuing down the current path of uncertainty has consequences for how and by whom this antiviral should be used. However, by applying lessons learned from the early days of the pandemic — including acknowledging the importance of randomized controlled trials (RCTs) — we can avoid repeating the same mistakes. To do this, it is necessary to start by defining the question, identifying current knowledge gaps, and only then can one propose scientific solutions to bring a rapid resolution to the COVID-19 rebound controversy.  (See link for article)

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**Comment**

Aside from the ever-mounting cases of Paxlovid rebound, Drs. Marik and Kory have been shouting from the rooftops about the dangers of taking Paxlovid. Said Dr. Kory in another recent Op-Ed:

“The problems with Paxlovid are no secret. FDA granted Pfizer emergency use authorization for the drug after a single trial with questionable results. The medicine has many contraindications, meaning it can’t be taken by someone who simultaneously would be taking certain anti-depressants, anti-seizure, anti-psychotic, cholesterol, or blood pressure medications. Furthermore, many Americans cannot take Paxlovid, given that nearly half of adults have cardiovascular disease.

“Consider the Food and Drug Administration’s recent decision allowing pharmacists to play doctor and prescribe Pfizer’s anti-viral treatment Paxlovid. No pharmacist could ever safely dispense a novel medicine with an unprecedented amount of drug interactions without in-depth knowledge of the severity of the patient’s medical problems or the critical necessity of each of their other medicines.

“Biden’s policy of a toxic jab in every arm and a pricey pill in every mouth needs an overhaul.”

Early treatment works. The FLCCC Protocols work. And hundreds of thousands are alive today to prove it.

But rather than take a cheap, effective, safe drug (ivermectin among others) – politicians continue to push expensive injections and medicines that not only don’t work, but are dangerous.

Category:

Treatment, Viruses

Destroying the Village in Order to Save It: Collateral Damage in the Battle Over Lyme Disease

https://academic.oup.com/ofid/article/9/5/ofac153/6551241

Destroying the Village in Order to Save It: Collateral Damage in the Battle Over Lyme Disease

Ross M Boyce
Open Forum Infectious Diseases, Volume 9, Issue 5, May 2022, ofac153, https://doi.org/10.1093/ofid/ofac153
Published:  21 March 2022

Abstract

A federal court recently dismissed the case against the Infectious Diseases Society of America (IDSA) brought by a group of patients with Lyme disease. While the outcome represented an important victory of the IDSA, I argue that it should also serve as a turning point in our approach to patients with “chronic” Lyme disease, many of whom experience substantial symptoms and suffer an emotional burden due to the uncertainty of their diagnosis. As the incidence of Lyme disease continues to increase and the geographic range of the vector expands, infectious disease specialists—experts in history taking, physical examination, and diagnosis—should play a leading role, not only to combat pervasive misinformation, but more importantly to benefit patients.

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For more:

Category:

Lyme, research

Emerging Tick Borne Diseases in Australia

http://

Emerging Tick Borne Diseases in Australia

Aug. 1, 2022

Dr. Peter Mayne

This recently uploaded video is about a 2011 paper found here:  https://www.researchgate.net/publication/221768948_Emerging_incidence_of_Lyme_borreliosis_babesiosis_bartonellosis_and_granulocytic_ehrlichiosis_in_Australia

Abstract

Borrelia burgdorferi, the causative agent of Lyme disease (LD), and Babesia, Bartonella, and Ehrlichia species (spp.) are recognized tick-borne pathogens in humans worldwide. Using serology and molecular testing, the incidence of these pathogens was investigated in symptomatic patients from Australia. Sera were analyzed by an immunofluorescent antibody assay (IFA) followed by immunoglobulin (Ig)G and IgM Western blot (WB) assays. Both whole blood and sera were analyzed for detection of specific Borrelia spp. DNA using multiplex polymerase chain reaction (PCR) testing. Simultaneously, patients were tested for Babesia microti, Babesia duncani, Anaplasma phagocytophilum, Ehrlichia chaffeensis, and Bartonella henselae infection by IgG and IgM IFA serology, PCR, and fluorescent in situ hybridization (FISH). Most patients reported symptom onset in Australia without recent overseas travel.
  • 28 of 51 (55%) tested positive for LD
  • Of 41 patients tested for tick-borne coinfections, 13 (32%) were positive for Babesia spp
  • nine (22%) were positive for Bartonella spp
  • Twenty-five patients were tested for Ehrlichia spp. and (16%) were positive for Anaplasma phagocytophilum while none were positive for Ehrlichia chaffeensis.
  • Among the 51 patients tested for LD, 21 (41%) had evidence of more than one tick-borne infection.
  • Positive tests for LD, Babesia duncani, Babesia microti, and Bartonella henselae were demonstrated in an individual who had never left the state of Queensland.
  • Positive testing for these pathogens was found in three others whose movements were restricted to the east coast of Australia.

The study identified a much larger tick-borne disease (TBD) burden within the Australian community than hitherto reported. In particular, the first cases of endemic human Babesia and Bartonella disease in Australia with coexisting Borrelia infection are described, thus defining current hidden and unrecognized components of TBD and demonstrating local acquisition in patients who have never been abroad.

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**Comment**

I repost this because “the powers that be” in Australia continue to downplay and deny that Lyme exists in Australia, despite the plethora of suffering patients and many doctors who state otherwise.  (Remember, there are many, many strains of borrelia or Lyme)

Please see this recent article, “Growing evidence of an emerging tick-borne disease that causes a Lyme-like
illness for many Australia patients,” by  Professor Noel. Campbell

It appears Mayne has also been disciplined for his stance on Lyme, like many other LLMDs.

Mayne states he has absolute proof that Lyme is in Australia as tissue samples at the bite sites that he took from two patients were positive for Lyme from DNA analysis.

Category:

Babesia, Bartonella, Ehrlichiosis, Lyme, research, Uncategorized

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