Archive for the ‘vaccines’ Category

J&J Lead Scientist Confesses: COVID Shot ‘Not Safe and Effective.’ Reveals ‘Lack of Research’

https://okeefemediagroup.com/johnson-johnson-lead-scientist/

BREAKING: Johnson & Johnson Lead Scientist Confesses J&J COVID-19 Vaccine Was ‘Not Safe and Effective,’ Reveals “Lack of Research” From Rushing to Release Vaccine: “People Wanted It, We Gave It to Them”

July 15, 2025

“We didn’t do the typical tests,” said Joshua Rys, a Lead Scientist in Regulatory Affairs for Johnson & Johnson (J&J), revealed on hidden camera that the typical clinical process was abandoned for the COVID-19 vaccine, knowingly bypassing standard testing protocols under pressure from the U.S. government and public demand. He added, “This was just, ‘let’s test it on some lab models… and just throw it to the wind and see what happens.’”

He acknowledged that the public wasn’t informed about the shortcuts, asking, “Do you have any idea the lack of research that was done on those products?” Rys claimed, “People wanted it, we gave it to them.”

While public officials claimed the vaccines were “safe and effective,” Rys pushed back. “There’s no proof. None of that stuff was safe and effective,” he said, adding that the industry relies on a benefit-risk tradeoff to justify product launches.

Rys also pointed to government pressure through Operation Warp Speed. “The government is like, ‘We need help… You’re solving this problem,’” he said. “People panic, so they try to solve it in whatever way they think is good.”

According to a U.S. Department of Health and Human Services (HHS) spokesperson, “Even during a public health emergency, pharmaceutical companies are still required to follow strict protocols for clinical testing. For emergency use, companies must show that the benefits clearly outweigh the risks. Oversight doesn’t stop at approval — the FDA and other agencies also monitor products closely once they’re in use. That includes real-world safety tracking, independent advisory committees, and required reporting of any adverse events. These steps are in place to make sure public health decisions are based on solid science and strong safeguards — especially in emergencies.”  (See link for video and article)

______________

**Comment**

None of this is new news other than the fact an undercover reporter got it straight out of the horse’s mouth.  

Go here for 20 studies by the McCullough Foundation on COVID shot harm. (On page 2)

For more:

It’s become beyond clear that these shots are not effective, do not stop transmission, are highly contaminated, should be declared ‘kill shots,‘ and taken off the market.

Category:

Activism, vaccines

Bill Filed to Repeal PREP Act & Strip Big Pharma of Legal Immunity

https://www.thefocalpoints.com/p/breaking-rep-massie-files-bill-to?

BREAKING: Rep. Massie Files Bill to REPEAL the PREP Act and Strip Big Pharma of Legal Immunity

The PREP Repeal Act (H.R. 4388) would END liability protections for experimental pandemic countermeasures like mRNA injections — and restore the right to sue for injury.

Jul 15, 2025

Rep. Thomas Massie (R-KY) has introduced the PREP Repeal Act (H.R. 4388), a landmark piece of legislation that would fully repeal the Public Readiness and Emergency Preparedness (PREP) Act — the federal law that grants sweeping legal immunity to pharmaceutical companies for injuries caused by emergency medical countermeasures, including mRNA injections.

“The PREP Act is medical malpractice martial law,” said Rep. Massie.

“The 2005 PREP Act prevents people from holding corporations accountable for the pain and suffering they cause during Presidentially declared emergencies. Americans deserve the right to seek justice when injured by government-mandated products. The PREP Repeal Act will restore that right.”

What the PREP Repeal Act Would Do:

  • Fully repeals Sections 319F–3 and 319F–4 of the Public Health Service Act — ending liability protections for pandemic countermeasures.
  • Restores the right to sue under federal and state law for injuries caused by drugs, biologics, or PREP Act–covered products.
  • Applies retroactively to pending lawsuits and appeals.
  • Rescinds unused federal funds from the PREP Act injury compensation fund.
  • Includes a severability clause to ensure the bill survives court challenges.

The PREP Repeal Act could be the single most important health freedom bill in Congress. It would dismantle a key pillar of the Bio-Pharmaceutical Complex, end blanket immunity for vaccine manufacturers, and bring long-overdue accountability for harm.

Supporting this bill is essential to restoring integrity and accountability in public health.

You can read the full bill text here.

Category:

Activism, vaccines

Mayo Clinic Lyme Disease Clap-Trap Part 2

https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/u/33710626?

Tomorrow’s Cure: New frontiers in Lyme disease detection — just in time for summer (Part 2)

Carl Tuttle
Hudson, NH, United States
Jul 16, 2025

Follow-up email to Cathy Wurzer, Host of Mayo Clinic’s “Tomorrow’s Cure” podcast.

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: “tomorrowscure@mayo.edu” <tomorrowscure@mayo.edu>
Cc: “newsbureau@mayo.edu” <newsbureau@mayo.edu>, “cwurzer@mpr.org” <cwurzer@mpr.org>, “asteere@mgh.harvard.edu” <asteere@mgh.harvard.edu>, “Pritt.bobbi@mayo.edu” <Pritt.bobbi@mayo.edu>
Date: 07/15/2025 10:44 AM EDT
Subject: Re: Tomorrow’s Cure: New frontiers in Lyme disease detection — just in time for summer

To: Cathy Wurzer,

Here are additional facts you are probably not aware of…

It is believed that Lyme disease was pigeonholed into its current status by the two principal investigators of the previous Lyme disease vaccines as these investigators conceptualized a disease that would enable vaccine development.

A preventive vaccine for Lyme disease would not satisfy the FDA if a chronic persistent infection and seronegative disease exist. Dr. Gary Wormser, lead author of the one-size-fits-all IDSA Lyme treatment guideline (which matches the conceptualized disease) was the principal investigator of Connaught’s Lyme vaccine which never made it to market. This is a flagrant conflict of interest. Have we been dealing with an antibiotic resistant/tolerant superbug purposely concealed to promote vaccine development?

Wormser received Grant# R01CK00015201 from the CDC totaling 1.5 million to produce the following junk science: (It is no secret that the CDC is in the shot business)
 
Subjective symptoms after treatment of EARLY Lyme disease.
https://www.ncbi.nlm.nih.gov/pubmed/20102996

Gary Wormser, New York Medical College

(Financed by the U.S. Centers for Disease Control)

RESULTS: 

“At 12 months after enrollment, only 5 (2.2%) of 230 evaluable patients reported new or increased symptoms, and in none of the patients were these symptoms of sufficient severity to be functionally disabling”

_____________________________

Summary of Wormser’s study: Anyone experiencing symptoms after the one-size-fits-all treatment approach is just experiencing nothing more than the “aches and pains of daily living.”

Post Treatment Lyme Disease Syndrome (PTLDS) after early treatment and untreated Lyme of months, years or decades are two entirely different disease states; the latter being ignored for three decades. Patients who have had a prolonged exposure to the pathogen are almost always incapacitated. So basically, Wormser’s results are then assumed to apply to the entire patient population; in other words, Lyme is no big deal which has wrongly influenced our nation’s response to this serious life-altering health threat. The research into how Lyme disables should have been completed by now but the misclassification of Lyme as a simple nuisance disease (hard to catch and easily treated) has paralyzed the response to this runaway plague. Purposely avoiding the advanced stage of disease hides the horribly disabled and anyone unable to see this is somewhat naïve.

When Wormser was appointed to the federal Tick-Borne Disease Working Group 12,393 angry individuals signed the petition to have him removed.
 
Remove Wormser from federal TBD working group (Please read!)
https://www.change.org/p/dr-richard-wolitski-remove-wormser-from-federal-tbd-working-group-due-to-financial-conflicts-of-interest  [See above picture of Wormser] 

The patient community is well aware of the mishandling of Lyme disease for the sake of a vaccine.

The New York Times Magazine
 
Stalking Dr. Steere

https://www.nytimes.com/2001/06/17/magazine/stalking-dr-steere.html

By David Grann   June 17, 2001

Last year, Dr. Allen Steere, one of the world’s most renowned medical researchers and rheumatologists, began to fear patients. It was not so much the ones he had treated, though he occasionally had to worry about them too, but the ones who had started to call his office, threatening him, claiming he was responsible for their suffering. They insisted that he was denying them treatment for an acute form of chronic Lyme disease, a strand of the ordinarily more modest infection that they believed slipped into the bloodstream undetected and remained there for years, causing joint pain, chronic fatigue, suicidal depression, paralysis and even death. Affirming their diagnoses were a growing number of patient advocacy groups, practitioners and psychiatrists who argued that the disease had become a full-scale epidemic, a modern-day plague crippling thousands of Americans.

Continued…

What I have shared here is just a fraction of the deliberate mismanagement uncovered in the fifteen years that I have studied the mishandling of Lyme disease.

None of this of course is mentioned in your Tomorrow’s Cure article.

Carl Tuttle
Independent Researcher
Hudson, NH

______________

**Comment**

Tuttle, per usual, is spot on.

To read part 1:  https://madisonarealymesupportgroup.com/2025/07/14/mayo-clinic-same-lyme-disease-clap-trap-just-in-time-for-summer/

Tuttle has also gone to the work of showing the conflicts of interest in 12 of the 14 authors of the IDSA Lyme Guidelines:   https://www.dropbox.com/scl/fi/swq4j8zz15hn56hp98jd2/12-of-14-IDSA-Lyme-guidelines-have-conflicts-of-interest.pdf?rlkey=yzqac1e01t6jw6wnmkckztjog&e=1&dl=0

It’s all right there in bright, purple crayon.

More on Dr. Wormser:

Category:

Activism, vaccines

DOJ Drops Charges Against Dr. Kirk Moore

https://childrenshealthdefense.org/defender/gnw-charges-dropped-utah-doctor-accused-destroying-covid-vaccines/

Charges Dropped Against Utah Doctor Accused of Destroying $28,000 in Covid Vaccines + More

The Defender’s Government NewsWatch delivers the latest headlines related to news and new developments coming out of federal agencies, including HHS, CDC, FDA, USDA, FCC and others. The views expressed in the below excerpts from other news sources do not necessarily reflect the views of The Defender. Our goal is to provide readers with breaking news that affects human health and the environment.

by The Defender Staff
July 14, 2025

Charges Dropped Against Utah Doctor Accused of Destroying $28,000 in Covid Vaccines

NBC News reported:

The federal government on Saturday dismissed charges against a Utah plastic surgeon accused of throwing away COVID-19 vaccines, giving children saline shots instead of the vaccine and selling faked vaccination cards. U.S. Attorney General Pam Bondi said in a post on the social media platform X that charges against Dr. Michael Kirk Moore, of Midvale, Utah, were dismissed at her direction.

Moore and other defendants faced up to 35 years in prison after being charged with conspiracy to defraud the government; conspiracy to convert, sell, convey and dispose of government property; and aiding and abetting in those efforts. The charges were brought when Joe Biden was president.

“Dr. Moore gave his patients a choice when the federal government refused to do so,” Bondi wrote. “He did not deserve the years in prison he was facing. It ends today.”  (See link for article)

_______________

**Comment**

Dr. Moore was imprisoned for 22 days for disobeying unethical orders to inject humans with a never before used gene therapy injection that were not properly tested for transmission, effectiveness and safety and were rushed to market.  In fact, studies showing efficacy were fraudulently done and they are highly contaminated. The package inserts were blank, yet we were told to simply ‘trust the experts’ and roll up our sleeves!  BTW: this information was hard for me to find and only The Wellness Company writes honestly about the blank package inserts.  Every other mainstream media outlet I read is dishonest about the inserts.

For more:

Category:

Activism, vaccines, Viruses

Mayo Clinic: Same Lyme Disease Clap-Trap Just in Time For Summer

https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/u/33704283?

Tomorrow’s Cure: New frontiers in Lyme disease detection — just in time for summer

Carl Tuttle
Hudson, NH, United States
Jul 14, 2025

What has been presented here in Tomorrow’s Cure is the same old dogma propagated for decades by those who have controlled this false public heath narrative.

Dr. Allen Steere would be doing us all a favor by retiring.

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: “tomorrowscure@mayo.edu” <tomorrowscure@mayo.edu>
Cc: “newsbureau@mayo.edu” <newsbureau@mayo.edu>, “cwurzer@mpr.org” <cwurzer@mpr.org>, “asteere@mgh.harvard.edu” <asteere@mgh.harvard.edu>, “Pritt.bobbi@mayo.edu” <Pritt.bobbi@mayo.edu>
Date: 07/13/2025 3:00 PM EDT
Subject: Tomorrow’s Cure: New frontiers in Lyme disease detection — just in time for summer

Tomorrow’s Cure: New frontiers in Lyme disease detection — just in time for summer

Deb Balzer July 2, 2025
https://newsnetwork.mayoclinic.org/discussion/tomorrows-cure-new-frontiers-in-lyme-disease-detection-just-in-time-for-summer/

“Dr. Steere identified Lyme disease in 1976 while investigating a cluster of children in Lyme, Connecticut, who were experiencing unexplained arthritis. His research ultimately led to the discovery and naming of the disease. Since then, researchers have devoted their efforts to advancing diagnostic tools, treatments and vaccine development.”

Mayo Clinic “Tomorrow’s Cure” podcast
Attn: Cathy Wurzer, Host

Dear Cathy,

Thirty-five  years ago Dr. Allen Steere identified chronic Lyme disease which should have set off a red flag prompting an immediate search for better antimicrobials but then did a 180° as he became principal investigator (PI) of the Phase 3 clinical trial for the first Lyme disease vaccine. So all the eggs were put into the vaccine basket while a campaign was orchestrated to discredit the sick and disabled patient population along with the courageous clinicians attempting to help these patients. Apparently, a chronic relapsing seronegative disease did not fit the business model of patent royalties, vaccine development and pharmaceutical profits. That rush to create a Lyme vaccine early in the discovery phase (of the Lyme epidemic) eliminated the research desperately needed to find a cure for an infection that was not responding to antibiotic treatment as reported by Dr. Allen Steere in 1990 and the disabled Lyme community ever since.

Here is Dr. Steere’s 1990 publication summary for your review:

The New England Journal of Medicine 

Published November 22, 1990

Chronic neurologic manifestations of Lyme disease
https://www.nejm.org/doi/full/10.1056/NEJM199011223232102

This is what Steere was reporting in 1977:

Lyme arthritis: an epidemic of oligoarticular arthritis in children and adults in three connecticut communities. (1977)
Steere AC, Malawista SE, Snydman DR, Shope RE, Andiman WA, Ross MR, Steele FM.
https://www.ncbi.nlm.nih.gov/pubmed/836338

Excerpt:

“The best treatment for this illness is not clear. Some physicians have reported that penicillin or tetracycline results in disappearance of the skin lesion (41,42), but others find antibiotics ineffective. Four of the patients with expanding skin lesions received penicillin but still developed arthritis.”

__________________________

In 1991 the Lyme disease organism, Borrelia burgdorferi, was grown from the cerebrospinal fluid of Lyme patient Vicki Logan at the Centers for Disease Control in Fort Collins, Colorado despite prior treatment with intravenous antibiotics. The patient died when the insurer refused additional IV antibiotics. Here is a copy of Logan’s CDC positive culture report for your review.

(Vicki Logan’s Chronic Lyme Autopsy results Page #1, 2, 3, 4, 5, 6, 7)

The destructive nature of Borrelia is evident in Vicky Logan’s liver (nutmeg liver), kidneys, heart, lungs and brain. The patient died after the insurer refused additional IV antibiotic therapy.

There are 700 peer-reviewed publications referencing persistent infection and in a 2018 study all patients were culture positive even after multiple years on antibiotics so there was no relief from current antimicrobials. Some of these patients had taken as many as eleven different types of antibiotics.

Quotes from the Tomorrow’s Cure podcast

Lyme disease testing:

Quote from Dr Pritt @ 15:11min into the podcast…

“…but later on, the antibody tests that we have are quite good at detecting those late-stage manifestations…”

1. Serology is so unreliable that in 2013 Virginia Governor Bob McDonnell signed HB1933 into law requiring healthcare providers to notify those tested that current laboratory testing can produce false negatives.

2. Governor Chris Sununu’s 2020-2021 commission to study diagnostic testing for Lyme disease  concluded that the FDA approved two-tier serologic immunoassay for Lyme was not reliable in all stages of disease; no better than a coin toss.
 
3. Peer-reviewed evidence of “Seronegativity in Lyme borreliosis and Other Spirochetal Infections” 16 September 2003  https://www.dropbox.com/s/3d6m45jzlhhwalu/Seronegativity.pdf?dl=0

4. I would like to point out the following case study from Stony Brook Lyme clinic. I understand the patient received thirteen spinal taps, multiple courses of IV and oral meds, and relapsed after each one, proven by CSF antigens and/or PCR. The only way this patient (said to be a physician) remained in remission was to keep her on open ended clarithromycin- was on it for 22 months by the time of publication.

Seronegative Chronic Relapsing Neuroborreliosis.
https://www.ncbi.nlm.nih.gov/pubmed/7796837

Lawrence C.a · Lipton R.B.b · Lowy F.D.c · Coyle P.K.d

aDepartment of Medicine, bDepartment of Neurology, and cDivision of Infectious Diseases, Albert Einstein College of Medicine, and dDepartment of Neurology, State University of New York at Stony Brook, New York, NY., USA

Eur Neurol 1995; 35:113–117 (DOI:10.1159/000117104)

Abstract

We report an unusual patient with evidence of Borrelia burgdorferi infection who experienced repeated neurologic relapses despite aggressive antibiotic therapy. Each course of therapy was associated with a Jarisch-Herxheimer-like reaction. Although the patient never had detectable free antibodies to B. burgdorferi in serum or spinal fluid, the CSF was positive on multiple occasions for complexed anti-B. burgdorferi antibodies, B. burgdorferi nucleic acids and free antigen.

Lyme disease vaccines:

Quotes from Dr Steere:

@ 26:41min: “I think we’ve had an effective and save vaccine for Lyme disease for over twenty years.”

@ 27:49 min: “From antivaccine movements the manufacturer decided it just was not worth the risk.”

This was not an “antivaccine movement” as there was substantial risk of serious harm to public health!

REPORT ON LYlMErix
Prepared by: SHELLER, LUDWIG & BADEY
Submitted to: VACCINES AN-D RELATED BIOLOGICAL PRODUSTS ADVISORY COMMITTEE   Jan 31, 2001

Excerpt:

The people who have contacted us were, prior to vaccination with LYMErix, healthy, active and energetic. Indeed, the very reason they sought the LYMErix vaccine was their desire to preserve their healthy, active lifestyle. However, what they experienced was a dramatic degradation of their health and quality of life. As will be described below, these previously healthy individuals are now afflicted with painful, at times debilitating arthritic symptoms, including joint pain and swelling, as well as extremely severe Lyme-disease-like symptoms which have persisted to this day.

LymeRix Vaccine Victim’s Stories and Related- Articles
https://www.dropbox.com/scl/fi/0jxjhg58v4zey5bl3s1xj/LYMErix-Vaccine-Victims-Stories-FDA-Jan-2001.pdf?rlkey=vmicwpln1e850otvtal0mw9y6&dl=0

JUDGEMENT, FINAL ORDER AND DECREE GRANTING FINAL APPROVAL OF THE CLASS ACTION SETTLEMENT:
https://www.lymedisease.org/wp-content/uploads/2018/05/2003-Vaccine-Judgement.pdf

What has been presented here in Tomorrow’s Cure is the same old dogma propagated for decades by those who have controlled this false public heath narrative.

Mark Twain once said, “It is easier to fool people than to convince them that they have been fooled.”

Has the wool been pulled over your eyes Cathy Wurzer?

Carl Tuttle
Independent Researcher
Hudson, NH
 
Letter to the editor published in BMJ June 10, 2020
Re: Lyme borreliosis: diagnosis and management
https://www.bmj.com/content/369/bmj.m1041/rr-1

Category:

Activism, Lyme, vaccines