Archive for the ‘Activism’ Category

Why the WHO Treaty Should Be Canned in 3.5 Minutes

https://freedomresearch.substack.com/p/freedom-research-tv-dr-meryl-nass  Video and Transcript Here (3.5 Min)

Why the WHO Treaty Should Be Canned

The WHO new treaties do not make sense medically, but would allow massive amounts of power and authority to be centered in the WHO, Dr. Nass warns.

The new so-called pandemic treaty and amendments to the International Health Regulations (IHR) – both are discussed right now at the World Health Organization (WHO). And the public is not being honestly informed about them, according to Dr. Meryl Nass. Dr. Nass is an internal medicine physician with extensive experience in a variety of fields, including vaccines and vaccine safety, epidemics, and disease outbreaks. She is one of the few medical professionals raising alarm about the new WHO treaties.

While today was the deadline for the WHO member states to notify the WHO about their rejection of the first changes to the IHR, in regards to shortening the term for the IHR amendments to become effective, the main changes as well as the new pandemic treaty are still being discussed. Both should be rejected, Dr. Nass says.

This is an excerpt from a longer interview with Dr. Nass. The full interview will also be published soon.

For more:

The Greatest Organized Crime in History: Review of “The Wuhan Cover-up” & Why Cover Up Vaccine Injuries?

https://petermcculloughmd.substack.com/p/the-greatest-organized-crime-in-history?

The Greatest Organized Crime In History

Review of “The Wuhan Cover-Up,” by Robert F. Kennedy, Jr.

JOHN LEAKE

The true story documented in Robert F. Kennedy, Jr.’s new book, The Wuhan Cover-Uphas long reminded me of the Max Frisch play, Biedermann and the Arsonists, in which decent, middle-class people are unable to detect the arsonists who are hiding in plain sight. As one of the arsonists remarks: “The best disguise, even better than humor and sentimentality, is the truth, because no one believes it.”

Many Americans are still struggling to believe that the cadre of “biosecurity experts” and pharmaceutical company bosses who directed the pandemic response were the same guys who created SARS-CoV-2—the causative agent of COVID-19.

This cadre reminds me of John Leonard Orr—the fire captain and arson investigator in Glendale, California who is believed to have set 2,000 fires in a 30-year arson spree while serving as a key, official investigator of the incidents.

After Wuhan, China was identified as the disease epicenter, the WHO sent a delegation led by Dr. Peter Daszak to investigate the pathogen’s origin—the same Dr. Peter Daszak whose EcoHealth Alliance had played an instrumental role in creating it. Not surprisingly, Daszak and his colleagues concluded that a lab leak was “highly unlikely.”

To be sure, it is very difficult for decent people to grasp that their government agencies—including Health and Human Services, the National Institutes of Health, and the Department of Defense—are indistinguishable from a mafia racket.

The Wuhan Cover-Up is an invaluable book because it documents in painstaking detail how this mafia racket came about, and how its activities culminated in the creation and escape of SARS-CoV-2 from a lab in Wuhan. The genesis of this racket is rooted in two basic elements:

1). The state’s incorrigible proclivity for expanding military power and waging war.

2). The fear of infectious disease.  (See link for article)

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**Comment**

I’m thankful for Leake’s undertaking as I find it hard to wade through Kennedy’s writings. I attempted his “The Real Anthony Fauci,” but set it aside due to the wordiness and vitriol.  I’m already angry and don’t need anything to add to it.  I need writings about this debacle to be “just the facts, mam, just the facts.”  If you haven’t learned it yet, you will: stress is a killer and one must be careful what eyes see, and ears hear.

Someone needed to get this down in pen and ink for those willing to learn and for those in the future looking back at this crazy COVID era.  The hope and goal of which is to prevent it from ever happening again; however, the methods these evil actors used are not new and have been deployed for decades as witnessed by Lyme/MSIDS patients and the doctors who dare treat them.

We’ve had a front-row seat for 3 years and running on the mafioso tactics of an out of control government using the very agencies created to protect the public.  They then hijacked science, the media, and medicine entirely – leaving only the few rugged individualists who refuse to bow to the system.  The take-over was complete and most people don’t have a clue.  

Like water finds the path of least resistance, patients will simply have to continue to go around a corrupt and monolithic system to find true, meaningful help.  For those in Lymeland, this is nothing new.  The problem of course is time, money, and wisdom – all of which are in short supply for most patients.

If ever there was a time to help each other, it is now.  For those who have their brain function, help those who don’t.  For those with energy, stand up for those who don’t have any, and do what you can in your little corner of the world to be an advocate.  There are far more of us than them and we all make a difference.

And thank God for those standing up to the tyranny and taking the punches for doing so!

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https://childrenshealthdefense.org/defender/government-big-pharma-vaccine-injury-cover-up-cola/?

Why Does the Government Cover Up Vaccine Injuries?

Reviewing a Century of Vaccine Disasters and the Early Trailblazers who Fought Against Them

Story at a glance:

  • Something about vaccines (e.g., their promise of a simple injection being sufficient to safely and effectively end all diseases) has always deeply appealed to the minds of government officials.
  • Unfortunately, that promise is often a lie, so over and over, unsafe and ineffective vaccines enter the market. When this happens, the officials who are invested in them do everything they can to protect the vaccines from scrutiny and cover up each red flag that emerges (e.g., by silencing their own scientists).
  • In previous decades, the press was much less corrupt than it is now and occasionally would air real investigations into what happened. I collected many of them (which I hope you can watch) because of how closely they match what is happening now.
  • Since those TV programs made many who were suffering from the vaccine injuries realize they were not alone, this created a massive PR problem for those officials — which was eventually solved by preventing any future segments from airing. This article was written in the hope that collective amnesia could be broken.  (See link for article)

Go here to read about the mass censorship of COVID by the media:

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https://www.midwesterndoctor.com/p/when-did-the-media-stop-covering-ad7

When Did the Media Stop Covering Vaccine Disasters?

How different would the world be if the pharmaceutical industry had not bought out the media?

I recently published an article which highlighted many instances where a dangerous vaccine was pushed on America and how eventually the mass media decided to air a report discussing the harms of those vaccines and the government’s willful disregard of all the evidence showing what was happening was a really bad idea. In turn, each of those reports ended the vaccination campaign.

Given that the COVID-19 vaccines were much more dangerous than any of those vaccines, and unlike the previous, were mandated upon America, it is hence extraordinary that the entire media (with the exception of a few hosts on Fox News) has never touched upon what is happening now—instead they typically attack anyone who points it out.

I would argue this shift is because the industry learned from each of those past vaccines disasters and realized that it was necessary to do each of the following:

  • Have better sales pitches. For example, in the videos featured below from the Bush administration, it is clear the language that are using to sell their dangerous emergency vaccine was sculpted by professionals. However, it’s also clear that language was not good enough and was significantly refined by the time of Operation Warp Speed.
  • Have complete immunity for the manufacturers (the COVID vaccines utilized the newly created Emergency Use Authorization regulations).
  • Not permit any critical coverage of the vaccines in the press as that instantly turned the public against the vaccines, something which was accomplished by the Clinton administration legalizing direct to consumer pharmaceutical advertising in 1997 (which to this day is only legal in the USA and New Zealand). Before long, those advertisements comprised most of the advertising money for the news networks and something the pharmaceutical industry was all too eager to leverage so its dubious products would never again be scrutinized.  (See link for article)

________________

**Comment**

A midwestern doctor goes through the various vaccines, their histories, and sordid back-stories.  Important vaccine education that all should be aware of because you will not hear this from bought-out Big Pharma doctors.

For m

For More:

Will Congress Recognize that Food is Medicine?

https://anh-usa.org/will-congress-recognize-that-food-is-medicine/

Will Congress Recognize that Food is Medicine?

Will Congress Recognize that Food is Medicine?

Two recent studies provide further evidence for the ancient maxim “Let food be thy medicine.” It’s time for Congress to take concrete steps towards recognizing the truth in those wordsAction Alert!

The studies, one from Tufts University and a second from the Public Health Institute(PHI), found substantial health and economic benefits from using food to both treat and prevent chronic disease. Shhh….don’t tell the FDA though, because the agency follows the letter of the law, and the law says if you talk publicly about the simple notion of using a food product as a medicine, that turns it into a drug! (Cherry and walnut growers found that out the hard way a few years back.) These results, added to the pile of evidence that has accrued over the years, are further justification for Congress to formally recognize that food is medicine and to expand consumer access to those kinds of healthcare options.

The studies looked at the effects of medically tailored meals (MTMs) and produce prescription programs to address diabetes and a host of other chronic diseases. MTMs are fully prepared, healthy meals for individuals living with conditions such as diabetes, heart failure, end-stage kidney disease, HIV infection, and cancer. Produce prescription programs provide discounted or free produce through electronic benefit cards or paper vouchers redeemable at grocery stores or farmers markets.

The Tufts study estimated that national implementation of MTMs could avert 1.6 million hospitalizations and save $13.6 billion in health care costs in the first year alone. Produce prescription programs, the authors found, could avert 292,000 cardiovascular events.

The PHI study, of its Healthy Food Rx project, similarly found that diabetic patients taking part in their produce prescription program reported statistically significant improvements in hemoglobin A1C and diabetes self-management activities. These included more physical activity, following a meal plan, and going to nutrition and diabetes management classes.

Consider the following from the Tufts report:

Poor nutrition is the leading driver of death and disability in the United States, including from heart disease, stroke, type 2 diabetes, obesity, hypertension, and some cancers, and has staggering costs to society. The economic costs of suboptimal diets due to health care spending and lost productivity are estimated at $1.1 trillion each year — equaling the economic output of the entire food sector… Today, 1 in 2 U.S. adults has diabetes or prediabetes, 3 in 4 [are overweight or obese], and 14 in 15 have suboptimal cardiometabolic health.

Translation: The wrong kind of food kills, the right kind of food is medicine! It’s a notion that’s integral to our DNA here at ANH, and we’re deeply concerned that the legal basis that determines what is a food and what is a drug is not fit for purpose. Over the last 70 or so years, the drug companies have stitched up legislation to make the scope of the definition so broad, it catches any product that helps prevent, mitigate, or treat disease. This gives the FDA, with its revolving doors with Big Pharma, carte blanche to go after any food product that makes a medicinal or drug claim, even if the science demonstrating this is indisputable. As we’ve seen, the agency is openly hostile to food-based medicines that we know work but haven’t had the millions it takes to go through FDA approval.

Some in Congress fortunately recognize that getting healthy food and supplements into the hands of Americans is something worth doing. Senator Kevin Cramer (R-ND) has reintroduced legislation to allow dietary supplements to be purchased with Health Savings Accounts (HSA), Flexible Savings Accounts (FSA), and Health Reimbursement Arrangements (HRA).

HSAs allow consumers to pay for current health care expenses and save for future expenses. They offer a number of advantages. First, HSA contributions are tax-deductible. Second, the interest earned on money in the account is tax-free. Third, tax-free withdrawals can be made for qualified medical expenses. HSAs are also a good way to put money aside for health expenses later in life, when these costs may increase. A Flexible Spending Account is a benefit that allows you to set aside money from your paycheck, pre-tax, to pay for healthcare expenses. An HRA is a type of HSA that is provided and owned by an employer.

Allowing HSAs, FSAs, and HRAs to cover the cost of dietary supplements will expand consumer access to products that can make us healthier. It is a small step toward a wider recognition among policymakers that food is medicine, and we’ve already started thinking seriously about how we might be able to initiate reforms to legislation and policy that are in line with the increasingly widely accepted notion that food is the cheapest, most effective and most accessible medicine available — bar none.

Action Alert! Write to Congress in support of expanded HSAs, FSAs, and HRAs. Please send your message immediately.  (Go to top link)

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**Comment**

This is a crucial issue for everyone, but particularly sick Lyme/MSIDS patients.

Effort is being made at every level to corrupt our food.  For more:

Post-Vaccination Syndrome: A Descriptive Analysis After COVID Shots

Again, caution must be used in reading the following article which calls the mRNA “vaccinations” against COVID-19 “safe” and effective, and that they “saved lives.”

“Authorities” used a plethora of  faulty data and faulty studies to make their claims.

Go here to see these injections are far from safe or effective, had no measurable impact on mortality, and here for the latest VAERS reports and mounting list of adverse reactions and death.  You’d have to be deaf, blind, AND dumb to state they are “safe and effective.”

Go here to read more about these “unintended immune responses” occurring which the authors insist have no “ill-effects.”

Tell that to all these people.

Lastly, many experts have been shouting about the dangers of mRNA technology which hijacks human cells, injects an operating system, and creates something that attacks the body, yet they are injecting animals, vegetables, and milk for human consumption with it despite the fact it has been shown to be transmissible through the GI tract.  Please read here about how these new proteins could be toxic or allergenic and have no good reason to be injected into anything we consume. 

Go here to take action.

________________

http://

Unexpected COVID Shot Complication

Dr. Phillip McMillan

The Pfizer vaccine can cause formation of abnormal proteins, not anticipated by the mRNA template.

The researchers in the following study are admitting, albeit subtly, that mRNA therapeutics cause “potentially harmful immune responses,” or else they wouldn’t be redesigning them to prevent such responses.

https://www.cam.ac.uk/research/news/researchers-redesign-future-mrna-therapeutics-to-prevent-potentially-harmful-immune-responses

Researchers Redesign Future mRNA Therapeutics to Prevent Potentially Harmful Immune Responses

Article Excerpts:

  • They found an unintended immune response occurred in one third of the 21 patients in the study who were vaccinated – but with no ill-effects, in keeping with the extensive safety data available on these COVID-19 vaccines.
  • The researchers identified that bases with a chemical modification called N1-methylpseudouridine – which are currently contained in mRNA therapies – are responsible for the ‘slips’ along the mRNA sequence.“We can remove the error-prone code from the mRNA in vaccines so the body will make the proteins we want for an immune response without inadvertently making other proteins as well. The safety concern for future mRNA medicines is that mis-directed immunity has huge potential to be harmful, so off-target immune responses should always be avoided.”

But everything we really need to know is right here:

This research was funded by the Medical Research Council and the Wellcome LEAP R3 programme, and supported by the NIHR Cambridge BRC.

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https://www.medrxiv.org/content/10.1101/2023.11.09.23298266v1

Post-Vaccination Syndrome: A Descriptive Analysis of Reported Symptoms and Patient Experiences After Covid-19 Immunization

Harlan M. KrumholzYilun WuMitsuaki SawanoRishi Shah, Tianna Zhou, Adith S. Arun, Pavan KhoslaShayaan KaleemAnushree VashistBornali Bhattacharjee, Qinglan DingYuan Lu,César Caraballo,Frederick WarnerChenxi HuangJeph HerrinDavid PutrinoDanice HertzBrianne DressenAkiko Iwasaki
Nov. 10, 2023

ABSTRACT

Introduction A chronic post-vaccination syndrome (PVS) after covid-19 vaccination has been reported but has yet to be well characterized.

Methods We included 241 individuals aged 18 and older who self-reported PVS after covid-19 vaccination and who joined the online Yale Listen to Immune, Symptom and Treatment Experiences Now (LISTEN) Study from May 2022 to July 2023. We summarized their demographics, health status, symptoms, treatments tried, and overall experience.

Results The median age of participants was 46 years (interquartile range [IQR]: 38 to 56), with 192 (80%) identifying as female, 209 (87%) as non-Hispanic White, and 211 (88%) from the United States. Among these participants with PVS, 127 (55%) had received the BNT162b2 [Pfizer-BioNTech] vaccine, and 86 (37%) received the mRNA-1273 [Moderna] vaccine. The median time from the day of index vaccination to symptom onset was three days (IQR: 1 day to 8 days). The time from vaccination to symptom survey completion was 595 days (IQR: 417 to 661 days). The median Euro-QoL visual analogue scale score was 50 (IQR: 39 to 70). The five most common symptoms were:

  • exercise intolerance (71%)
  • excessive fatigue (69%)
  • numbness (63%)
  • brain fog (63%)
  • neuropathy (63%)

In the week before survey completion, participants reported feeling:

  • unease (93%)
  • fearfulness (82%)
  • overwhelmed by worries (81%)
  • feelings of helplessness (80%)
  • anxiety (76%),
  • depression (76%)
  • hopelessness (72%)
  • worthlessness (49%) at least once

Participants reported a median of 20 (IQR: 13 to 30) interventions to treat their condition.

Conclusions In this study, individuals who reported PVS after covid-19 vaccination had low health status, high symptom burden, and high psychosocial stress despite trying many treatments. There is a need for continued investigation to understand and treat this condition.

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**Comment**

I’m sure this is all very “rare” and completely coincidental.  #ABV

Please go here to read one researcher’s theory that this could very well be a new Spike-Induced Amyloidosis.

Federal Oversight of Lab Tests Part 2

Go here for Part 1.

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

Medscape: New Federal Oversight of Lab Developed Tests (Part 2)

Carl Tuttle

Hudson, NH, United States

DEC 4, 2023 — 

Follow-up letter to Auwaerter’s Commentary on Medscape:

New Federal Oversight of Lab Developed Tests
https://www.medscape.com/viewarticle/997365

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: “pauwaert@jhmi.edu” <pauwaert@jhmi.edu>, “pgauwaerter@gmail.com” <pgauwaerter@gmail.com>
Cc: “aaguilar@webmd.net” <aaguilar@webmd.net>, “DFlapan@Medscape.net” <DFlapan@Medscape.net>, “lkane@medscape.net” <lkane@medscape.net>, “gamiller@medscape.net” <gamiller@medscape.net>, “dolmos@webmd.net” <dolmos@webmd.net>, “sarah.wright@webmd.net” <sarah.wright@webmd.net>, “editor2@webmd.net” <editor2@webmd.net>, “dqhh@westchestergov.com” <dqhh@westchestergov.com>, “jmm2@uab.edu” <jmm2@uab.edu>, “sarah.long@drexelmed.edu” <sarah.long@drexelmed.edu>, “scalderwood@partners.org” <scalderwood@partners.org>, “cbusky@idsociety.org” <cbusky@idsociety.org>, “tjohnson@idsociety.org” <tjohnson@idsociety.org>
Date: 11/01/2023 9:04 AM EDT
Subject: Re: Medscape: New Federal Oversight of Lab Developed Tests

“I often see patients who are concerned they might have Lyme disease, or they’ve been told by other physicians that they have a tickborne or multiple infections. I’ve had patients who claim to have five or six infections: Lyme disease, Babesia, Bartonella, Mycoplasma, or Epstein-Barr virus. -Dr. Paul Auwaerter/Medscape

Dr. Auwaerter,

The following recent study (15 Aug 2023) shows that “multiple tickborne infections” are common as a third of these 140 individuals had more than just Lyme disease. Only 52% of patients recalled having a tick bite, while 46% did not exhibit a bull’s-eye rash.

My inquiry to you that has gone unanswered:

What “FDA approved Tick-Borne Disease Panel” are you recommending so as not to miss any of these infections?

A Longitudinal Study of a Large Clinical Cohort of Patients with Lyme Disease and Tick-Borne Co-Infections Treated with Combination Antibiotics
https://www.mdpi.com/2076-2607/11/9/2152

Summary By Dr. Daniel Cameron:
https://danielcameronmd.com/how-effective-is-combination-antibiotic-treatment-for-tick-borne-infections/

In their article “A Longitudinal Study of a Large Clinical Cohort of Patients with Lyme Disease and Tick-Borne Co-Infections Treated with Combination Antibiotics” Xi and colleagues looked at 140 individuals who tested positive for tick-borne infections (TBI) with 33% of those patients infected with multiple TBIs.¹

The authors found that out of the 140 participants:

-93 (66.43%) had positive antibody responses to one tick-borne infection
-83 (59.29%) were positive for Borrelia
-7 (5.00%) were positive for Rickettsia
-1 (0.71%) each for either Babesia, Bartonella, or Ehrlichia

The remaining 47 (33.57%) patients were infected with multiple tick-borne infections, including Borrelia, Babesia, Bartonella, Ehrlichia and Rickettsia.

The majority of patients were treated with a triple antibiotic combination regimen.

Most of the participants received 500 mg cefuroxime, 300 mg rifampicin, and 300 mg lymecycline. Treatment duration ranged between 12 and 40 weeks.

In the first follow-up visit with 118 patients, 59% reported having pain and 41% had neurological symptoms. Meanwhile, there was continued improvement in patient symptoms at the second follow-up visit. Out of 101 patients, 41% reported having pain and 30% had neurological symptoms.

“There were statistically significant reductions in the incidence of pain and neurological symptoms between follow-ups,” the authors wrote.

“Thus, our study demonstrates that combination antibiotics effectively relieve TBI symptoms with good patient tolerance.”

According to the survey, 52% of patients recalled having a tick bite, while 46% did not exhibit a bull’s-eye rash.

The patients exhibited significant improvements in their health status during the first and second follow-up visits.

“The three most common symptoms reported by the patients were pain, fatigue, and neurological symptoms, such as a tingling sensation in the limbs and memory defects,” the authors wrote.

At the second follow-up visit, “The number of patients suffering from pain, neurological symptoms, and fatigue decreased by 41.43%, 37.50%, and 17.54%, respectively,” according to the authors.

The improvement in pain and neurological symptoms was significant but fatigue continued to be problematic for patients.

Authors Takeaways:

“Our study established that most patients in this cohort were infected with the Borrelia burgdorferi species, and about a third had co-infections with other tick-borne pathogens.”

“Approximately half of the patients recalled receiving a tick bite and developing a bull’s-eye rash.”

“Pain, fatigue, and neurological symptoms were among the most common persistent symptoms.”

Dr. Auwaerter,
 
What FDA approved Tick-Borne Disease Panel are you recommending so as not to miss any of these infections?

On 10/30/2023 10:21 AM EDT CARL TUTTLE <runagain@comcast.net> wrote:

Dr. Auwaerter,

Let me remind you that as Vice Chair representing the IDSA Foundation, you are required to respond to inquiries regarding any statements you make in public otherwise your credibility/integrity is in question.

Carl Tuttle

______________

And BOOM! Carl knocks the opponent out of the ring.