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.

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.

UPDATE: Go here to take action:   https://childrenshealthdefense.org/community/tell-ag-bondi-and-epa-administrator-zeldin-to-drop-epas-appeal-in-the-decision-against-fluoride/

Your tax dollars at work……

https://fluoridealert.org/content/epa-to-appeal-fluoride-lawsuit-on-july-18/

When the US district court ruled in our favor last September, it deemed fluoridated water an “unreasonable risk” to human health due to its neurotoxicity. The judge pointed out the scope of the potential harm:

“The size of the affected population is vast. Approximately 200 million Americans have fluoride intentionally added to their drinking water at a concentration of 0.7 mg/L…. Approximately two million pregnant women, and over 300,000 exclusively formula-fed babies are exposed to fluoridated water.” [p. 76]

Ever since the Fluoride Action Network (FAN) petitioned the US Environmental Protection Agency (EPA) to prohibit the use of fluoridation chemicals under the Toxic Substances Control Act (TSCA) in 2016, our goal has been to protect the public as quickly as possible. We understand that every day, hundreds of thousands of children are experiencing unnecessary life-long and potentially life-altering brain impairment due to artificial fluoridation schemes. Countless others are experiencing side-effects to their liver, kidneys, endocrine system, bones, and much more.

Unfortunately, the EPA has spent the last 9-years working against our efforts, battling FAN in court and choosing to delay the legal process at every opportunity. Since filing a Notice of Intent to Appeal just days before the January 2025 deadline to do so, the EPA requested, and was granted, four deadline extensions to submit a brief with their arguments, delaying the process an additional 3-months. They stated that the previous and current Solicitor Generals had not approved or authorized an appeal.

According to FAN attorney Michael Connett, the EPA has now received approval from Solicitor General John Sauer and plans to file their appeal on July 18, 2025. Michael Connett wrote:

“After several extensions, the Trump Administration has decided to appeal the federal court decision ordering EPA to address the risk posed by water fluoridation. EPA will be filing its appeal next Friday, July 18.

Rather than use the court’s decision as an opportunity to finally end water fluoridation (as most of Europe has already done), the EPA will spend its time legally challenging the court’s order. And it won’t be alone. The American Chemistry Council (a trade organization that represents the chemical industry) has just filed a motion asking for permission to file a brief. And so has the American Fluoridation Society, one of the most noxious lobbyist groups pushing fluoridation across the US.

The decision to appeal the court’s order was not made by the HHS or Secretary Kennedy. It was made by the Solicitor General of the Department of Justice, who reports to Pam Bondi and the White House. For his part, Secretary Kennedy has been clear that states should end their water fluoridation programs (as Florida and Utah have recently done), and that CDC will be revising its anachronistic recommendations, which would be a major development. The HHS does not, however, have the authority to ban fluoridation.

Only the EPA has this power, and it has decided, for now, to forego its historic opportunity (as provided by the court’s decision) to exercise it.

Our lawsuit against the EPA will thus continue, and will now be before the Ninth Circuit Court of Appeals. I had hoped this would not be necessary, but we are ready and prepared to stand up to EPA’s challenge.”

The appeal will be decided by a three-judge panel from the Ninth Circuit Court of Appeals for the Ninth Circuit. The appeal process generally takes 6-12 months to resolve, although there is no guarantee of that short of a time frame. While some cases are decided based exclusively on written documents, some cases are selected for short oral arguments before a court panel. With most cases, the court of appeals decision is the final ruling unless the parties ask the US Supreme Court to review it or the case is sent back to the trial court for additional proceedings.

FAN will share the EPA’s written arguments and our response when they’re filed.

EPA Administrator Lee Zeldin announced in April that the EPA will be using the Safe Drinking Water Act’s six-year-review process to “expeditiously review new scientific information on potential health risks of fluoride in drinking water,” adding that “When this is completed, we will have an updated foundational scientific evaluation that will inform the agency’s future steps,” which will likely include a new maximum contaminant level (MCL) and maximum contaminant level goal (MCLG), which limit the levels of potentially harmful contaminants–such as fluoride–that water treatment operators can have in public water supplies.

Only time will tell if the EPA’s upcoming review will have any bearing whatsoever on the EPA’s appeal over the coming months.

For more:

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:

UPDATE:  Renowned climate engineering researcher Dane Wigington says:

“With this event in Texas that has just happened, the climate engineers, aka weather terrorists, overplayed their hand yet again. Now people are truly taking notice.

Wigington says 40 million to 60 million tons a year are being sprayed into the atmosphere.

https://celiafarber.substack.com/p/cloudseeding-company-rainmaker-founded?

Cloudseeding Company “Rainmaker” Founded By 25 Year Old Thiel Fellow Augustus Doricko, Was Seeding In Texas Flood Areas 2 Days Before Flood: “Stewarding The Natural World.”

No Longer Can You Trust A Mullet: Meet The New Brilliant Lunatic, Frustrated He Can’t Play With Rain Without Any Red Tape– Leans “Libertarian,” And “Anti-Regulation.” Get Ready For Tech Christians

**Comment**
Again, I post information like this for three reasons 1) To educate and inform patients so they can make informed decisions and vote with wisdom 2) Show how man’s interventions are behind any climate issues, not nature 3) Show how spraying the skies with toxins will affect everyone, particularly sick Lyme/MSIDS patients
For more:

https://www.globallymealliance.org/news/why-you-can-cross-mosquitoes-off-your-lyme-disease-worry-list?

A new study finds no evidence that mosquitoes can transmitBorrelia burgdorferi, the bacterium that causes Lyme disease. This study reinforces that ticks are the only proven source of infection.

What did the study show?

Many Lyme disease patients have questioned whether a mosquito bite could have been the source of their infection, especially as many do not remember finding a tick. This new study published just this June in the journal Parasites & Vectors offers strong reassurance that mosquitoes are not capable of carrying or transmitting the Lyme disease bacteria, Borrelia burgdorferi. Even when exposed under lab conditions, the bacteria could not survive inside mosquitoes or be passed to mice.

A diagram of insects with text
AI-generated content may be incorrect., Picture

Graphical abstract from Pekľanská et al. (2025), “Experimental evidence rules out mosquitoes as vectors of Lyme disease,” Parasites & Vectors. Image reused under an open-access Creative Commons license (CC by 4.0).

Why does this matter?

It’s common for patients to be unsure of how or when they were infected, and that’s completely understandable. Many people don’t recall a tick bite because the deer tick nymphs responsible for most Lyme disease cases are very small (the size of a poppy seed!), and their bites often go unnoticed. With that in mind, knowing Lyme disease is only spread by ticks helps patients and families focus on the right prevention strategies and worry less about every mosquito or bug bite. 

How was the study done?

To find out if mosquitoes can spread Lyme disease, scientists ran a detailed series of lab experiments. First, they let different species of mosquitoes feed on mice infected with Lyme-causing bacteria. In some cases, a few mosquitoes did pick up the bacteria, but the numbers were extremely low and the bacteria quickly died during digestion.

The researchers also tested whether the bacteria could survive long enough to be passed on to a new host, either naturally or through interrupted feeding. In every case, the answer was no. The bacteria couldn’t stay alive or infectious inside mosquitoes, and they never made it into the saliva, which is the only way a mosquito can transmit disease. 

To make sure the experiment was working properly, the researchers also included infected deer ticks, which did successfully transmit the Lyme disease bacteria to mice. These findings confirm that mosquitoes cannot maintain or transmit the bacteria that cause Lyme disease.

What is the takeaway?

This research addresses a long-standing question within the Lyme disease community about the potential role of mosquitoes in transmission. By providing evidence that mosquitoes cannot serve as competent vectors for Borrelia burgdorferi, the findings help refine public health messaging and support prevention strategies that remain focused on tick exposure.

To learn how to protect yourself and your family from ticks, visit our guide on how to be Tick AWARE.

Publication: 
Pekľanská M, Kuníková K, Vlčková R, et al. Experimental evidence rules out mosquitoes as vectors of Lyme disease. Parasit Vectors. 2025;18(1):206. Published 2025 Jun 4. doi:10.1186/s13071-025-06823-x 
_______________
**Comment**
I find it incredibly sad that we are over 40 years into this madness and it took this long for this study to be done.  Sad.
We desperately need properly done transmission studies for all things Lyme/MSIDS.
One thing to keep in mind: the study found mosquitoes seemingly can not carry or transmit Lyme.  This could change in the future with different lab techniques and technology.  Science is forever changing.
And lastly, the article makes it appear that ticks are the ONLY way to get Lyme.  This is patently false as congenital transmission has been proven.  There is also much to indicate it can be transmitted sexually as well.
The fact transmission studies have not been done shows clearly how far behind we are in knowledge of this complex illness impacting more and more people every year.