Archive for the ‘Viruses’ Category

Massachusetts Officials Approve Curfew Due to EEE & Fauci Recovering from West Nile Virus

https://www.boston25news.com/news/local/despite-parental-pushback-officials-approve-curfew-mass-town-amid-critical-eee-risk

Despite parental pushback, officials approve curfew in Mass. town amid critical EEE risk

By Boston 25 News Staff

OXFORD, Mass. — Health officials in one of four Massachusetts communities facing a critical risk for Eastern Equine Encephalitis met Wednesday night at a special meeting to discuss measures to keep residents safe, ultimately approving a townwide curfew.

As of Wednesday, the towns of Oxford, Douglas, Sutton, and Webster were considered at critical risk for EEE, according to the latest Massachusetts arbovirus risk map.

The towns were elevated to the high-risk level after a man in his 80s recently tested positive for EEE last week.  (See link for article)

______________

**Comment**

The curfew set at 6pm will shift to 5pm starting Oct 1 and will last through the first frost.

Please note all of this due to one 80 year old man testing positive.

Please note that EEE is a nationally notifiable condition.  This means they are counting cases and keeping track of it.  Bartonella, on the other hand, isn’t, yet can make you miserable or kill you just the same.

The CDC webpages state:

  • Eastern equine encephalitis virus IgM testing is available commercially, at some state health departments, and at CDC.
  • A positive eastern equine encephalitis virus IgM test result should be confirmed by neutralizing antibody testing at a state public health laboratory or CDC.
  • Some patients who are severely immunocompromised might require molecular (e.g., RT-PCR) testing for diagnosis.
  • Most persons infected with eastern equine encephalitis virus have no apparent illness. Symptomatic persons typically develop a systemic febrile illness that can progress in <5% of individuals to meningitis or encephalitis. The incubation period for eastern equine encephalitis ranges from 4 to 10 days but can be several weeks in patients who are immunocompromised.
  • Signs and symptoms in patients with neuroinvasive disease can include headache, meningismus, confusion, focal neurologic deficits, seizures, and coma.
  • Eastern equine encephalitis should be considered in any person with an acute febrile or neurologic illness who has had recent exposure to mosquitoes, especially during the summer months in areas where virus activity has been reported.
  • EEE has a fatality rate of 30%.  Of those that recover, more than half are left with physical or neurologic sequelae.

The article doesn’t state how this elderly man was tested but I’ll bet my hat it was PCR, which inventor Kary Mullis states should never be used to diagnose anybody.

The article also doesn’t state whether this man even has symptoms or how severe they symptoms are.

Does all of this look and feel like deja vu?

It should.

________________

https://www.theguardian.com/us-news/article/2024/aug/24/anthony-fauci-west-nile-virus

Anthony Fauci recovering at home after hospitalization for West Nile virus

Former head of the NIH’s National Institute of Allergy and Infectious Disease is expected to make a full recovery

Anthony Fauci is recovering at home from a West Nile virus infection, a spokesperson told news outlets on Saturday.

The former head of the National Institutes of Health’s (NIH) National Institute of Allergy and Infectious Disease was hospitalized for six days with the virus. Fauci, 83, is expected to make a full recovery.

“Tony Fauci has been hospitalized with a case of West Nile virus. He is now home and is recovering. A full recovery is expected,” a spokesperson told multiple outlets.

Fauci retired from his role at the NIH in 2022 after achieving widespread recognition for his role in public health communication during the Covid-19 pandemic. He now serves as a distinguished professor at Georgetown University’s School of Medicine. (See link for article)

______________

**Comment**

CDC webpages state:

  • West Nile virus is the leading cause of mosquito-borne disease in the U.S.
  • Most people with West Nile do not feel sick.  (About 1 in 5 have fever and symptoms)
  • Symptoms include fever, headache, body aches, vomiting, diarrhea, or rash.
  • There are no vaccines to prevent or medicines to treat West Nile virus disease (West Nile) in people.

For more:

Please note that all sorts of shenanigans have been done for decades against mosquitoes and nobody knows the effects of these interventions.  As in the case of ‘vaccines,’ man-made interventions to kill bugs often have deleterious effects on biological health, which few are tracking.

Category:

Activism, mosquitoes, Transmission, Viruses

FDA Industry Guidance: Fraud Coordination Tools

https://bailiwicknews.substack.com/p/fdas-document-only-2010-definition

FDA’s document-only, 2010 definition of ‘viral vaccines;’ FDA’s 2007 recommendation that developers not assess whether vaccination causes autoimmune disease.

Katherine Watt
Aug 22, 2024

Aug. 22, 2024 Note 1

I do not believe that FDA “guidance for industry” documents are intended by FDA or construed by pharmaceutical manufacturers, as enforceable rules.

I believe they are written and published as part of the regulatory charade, and are one method through which FDA, DoD and pharmas coordinate the militarized fraud they are jointly perpetrating on the public.

I’m posting this 2010 FDA document-only definition of “viral vaccines” (FDA has not defined vaccine, or viral vaccine, in CFR regulations) because such definitions,

When viewed alongside the complete absence of physical standards and methods/techniques/equipment capable of determining product purity, safety and efficacy;

Which have not been established by FDA or by FDA’s allegedly private-sector partner, the US Pharmacopeia/National Formulary — see, for example, USP June 2020 Standards for Quality Vaccines–General Vaccine Development and Manufacturing, indicating the non-existence of measurable standards and measurement techniques by the phrase “Not intended to convey requirements enforceable by regulatory agencies;”

May help more people understand that vaccines, from the batch and lot level at the factories, through the vial and dose level when administered to a person, are intrinsically heterogeneous, unstable and toxic.

There is no safe dose of vaccine material.
There never will be.

(See link for article)

_________________

Go here:  The FDA’s War Against America’s Health

**Comment**

The COVID debacle and subsequent censorship has made good, independent journalism, science, and ethical behavior popular again.  There’s always a silver lining….

In this case, Katherine Watt digs through reams of boring, bureaucratic language to uncover the pervasive fraud perpetuated by government agencies entrusted with protecting the public.  Far from protecting the public, these agencies have utilized and created every loop-hold imaginable to man for their own vested interests, which doesn’t have a thing to do with public health.  Dr. Peter McCullough recently stated that at the top of a medical and bioscientific deep state is HHS of which the FDA and CDC report to.  The NIH, UNAID, and other governmental agencies are a big players as well, and they all take care of each other financially through grants, and other programs.

I highly recommend reading the entire article because you will discover:

  • There is absolutely no measurable standards enforceable for vaccine purity, safety, and efficacy.  It’s the wild West without the rule of law or even sheriffs.
  • The FDA & pharma officials, military officers and FDA’s allegedly private-sector partner, the US Pharmacopeia/National Formulary, have known for decades there is no safe dose for vaccines.
  • FDA ‘regulations’ are non-regulations that instruct pharma on how to ignore engage in acting designed to look like compliance.
  • The FDA will then pretend to establish and enforce said ‘regulations’.
  • In 2007 it was known that DNA ‘vaccines’ might cause or worsen organ-specific autoimmunity but the FDA ‘no longer recommend that preclinical studies be performed to specifically assess whether vaccination causes autoimmune disease.’
  • The FDA participates in ‘don’t ask, don’t tell’ regarding Pharma.
Remember, the FDA asked for over 50 years to release ‘vaccine’ safety data!

If it wasn’t for a group suing the FDA, we wouldn’t even know about it.

This is where things currently stand in the US. We have to take legal action against government groups entrusted with public health for any transparency whatsoever.

For more on the corrupt FDA:

Category:

Activism, vaccines, Viruses

Monkeypox Antivirals Under CDC Lockdown

https://popularrationalism.substack.com/p/cdc-has-monkeypox-antivirals-under?

CDC Has Monkeypox Antivirals Under Lockdown

The STOMP trial or CDC’s “expanded access protocols” are the only way to get treatments studied so far to patients. So far, one natural compound has been studied.

 
James Lyons-Weiler
Aug 22, 2024

In an unusual move, the CDC is holding a monopoly on access to drugs that might be useful in treating a contagious virus. Here, we explore standard-of-care options for treating monkeypox.

Physicians in the field have found that care primarily focuses on alleviating symptoms and preventing complications, as no specific antiviral treatment has been approved specifically for monkeypox.

Potential (proposed) guidelines for managing the condition:

1. Symptomatic Treatment:

– Pain and Fever Management: Over-the-counter pain relievers such as ibuprofen or acetaminophen can help manage pain and fever.

– Hydration: Ensuring adequate fluid intake to prevent dehydration is crucial.

– Skin Care: Keep the skin lesions clean and dry. Calamine lotion or antihistamines might be used to alleviate itching.

2. Isolation and Prevention:

Isolation: Patients should be isolated to prevent the spread of the virus, especially when they are symptomatic and have active lesions.

– Hygiene: Regular handwashing and disinfecting surfaces can help reduce transmission.

3. Antiviral Treatments:

Tecovirimat (TPOXX) is an antiviral medication approved for the treatment of smallpox. Due to its activity against orthopoxviruses, it is sometimes used under compassionate use or in clinical trials for monkeypox.

Cidofovir and Brincidofovir are antiviral drugs sometimes used to treat severe orthopoxvirus infections. Their use for monkeypox is not well established, but it is generally considered when other options are unavailable.

4. Supportive Care:

– Monitoring for Complications: Patients should be monitored for potential complications, such as bacterial infections of skin lesions, pneumonia, or encephalitis, especially in immunocompromised individuals.

– Hospitalization: Severe cases may require hospitalization for supportive care and treatment of complications.

5. Counseling and Mental Health Support:

– Psychological Support: Patients with monkeypox may require psychological support due to the stigma and isolation associated with the disease.  (See link for article)

_______________

**Comment**

The CDC monopolizing testing and treatment is its MO:

Category:

Activism, Treatment, Viruses

Similarities Between ‘Spike Protein’ and Synthetic Anthrax Toxin

https://sashalatypova.substack.com/p/some-similarities-between-spike-protein

Similarities between “spike protein” and synthetic anthrax toxin.

Real bioweapons are not viruses but chemical weapons.

Sasha Latypova
Aug 21, 2024

PREP Act declarations should be read as announcements of use of certain types of chemical-biological weapons of mass destruction. As my readers know, covid PREP Act declaration is currently active until Dec 31, 2024, but it will be for sure extended thereafter. Marburg and Ebola declarations are active until at least Dec 31, 2028.

There are several non-covid PREP Act declarations currently active: These declarations are for influenza, zika, insecticides/nerve agents, anthrax and botulism toxin. They were updated/re-issued on Dec 23, 2022, however for all of these agents, the original declarations had been issued many years ago, starting around 2008.

Both, manufacturers and users would have liability immunity.

Users of the first countermeasures being the DoD agents who did/do the dispersing of the aerosol, water-borne, food-borne poisons.

Users of the second countermeasures being the pharmacists, nurses, doctors, midwives, etc who did/do the injections falsely advertised as treatments for the first set of countermeasures.

This prompted me into looking at the literature and trying to see any patterns that would indicate that some of the toxins being covered under PREP Act declarations can be used to simulate “viral pandemics”.

I will briefly address the nerve agents first and then write more about interesting parallels between anthrax toxin and so-called “spike protein” purported to be the agent of both, covid illness and covid vaccine injury.  (See link for article)

______________

SUMMARY:

  • Latypova believes poisoning via chemical agents is a very plausible explanation for many historical ‘pandemics’ and ‘epidemics,’ however, she doesn’t believe these agents were used for simulating the COVID outbreak.
  • “PREP Act declarations are a key part of the “pandemic preparedness” racket run by the military-industrial mafia (International Medical Countermeasures Consortium) and propagandized on all sides of freedom by characters like Robert Malone.”
  • The biodefense mafia operates on word confusion.
  • Naturally occurring anthrax is a soil bacterium that exists as a spore but is not typically transmissible or dangerous.
  • In 10 years of targeted effort there’s been about 68 patients with anthrax found in China in a country of 1.3 billion and nobody died.
  • It is treatable with antibiotics and there is no need for vaccination.
  • The anthrax vaccine manufactured by Emergent is much more poisonous than naturally occurring anthrax.
  • What is made in a lab is a synthetic chemical toxin allegedly resembling a small part of b. anthracis.
  • Synthetic chemicals do not reproduce or spread or ‘leak’ by themselves. The best way to produce mass illness is by injection under the pretense of ‘vaccination.’
  • This is exactly what happened to Gulf War soldiers through anthrax vaccination.
  • Synthetic anthrax is a chemical weapon (toxin) that can be assembled from ‘legal’ components.
  • Animal studies showed that certain components of this synthetic anthrax are lethal above a certain dosage, other components produce a ‘mild clinical disease.’
    • The monkey study conducted at the University of New Mexico in 2014 used both synthetic and allegedly natural anthrax.  The ‘natural’ Ames strain (A.Br.Ames lineage) came from US Army, Ft. Detrick which originates predominantly in China.
  • Symptoms were: decreased appetite and activity level, a mild, dry cough, elevated C-reactive protein and neutrophil counts indicating an inflammatory response and low-level transient bacteremia.
  • Decreased appetite and rapid weight loss are the most characteristic of COVID poisoning.  These same symptoms were reported in rats in both Pfizer’s and Moderna’s vax studies.
  • There are similarities between the COVID spike protein and the anthrax toxin and both include the furin cleavage site.
  • Dr. Lee Merritt has been outspoken about COVID being a type of contact poison or toxin.  She also speaks prolifically about parasites.
  • Hopefully when people are aware that chemical poisoning can mimic and fake “infectious outbreaks” they will be less likely to fall for propaganda of “lab created viruses.”  (See link for article)

Category:

Activism, vaccines, Viruses

Aussie, German, Korean, Japanese, & Scandinavian Studies on COVID Shots: Excess Deaths, Organ Damage, Auto-Immunity, Myocarditis & Pericarditis, & Deadly Batches

https://childrenshealthdefense.org/defender/covid-vaccine-excess-deaths-australia/

Australian Researcher Finds Link Between COVID Vaccines and Excess Deaths

The number of excess deaths in Australia was positively correlated with the number of COVID-19 booster vaccinations, according to a new peer-reviewed study. However, critics cautioned that the study’s methods were too simplistic and that its results could be misleading.

by Suzanne Burdick, Ph.D.
AUGUST 15, 2024

Article excerpts:

Denis Rancourt, Ph.D., lead author of a recent study examining excess mortality in 125 countries, cautioned against drawing conclusions from Allen’s analysis. He told The Defender:

“This type of correlation analysis between bulk measures of excess mortality and vaccine doses administered has many caveats, pitfalls and known confounding factors.

“It should never be used as a stand-alone result, as was done here. On its own, it has a high likelihood of being misleading, and it does not imply any meaningful relation.”

Rancourt said that even if a relationship exists between COVID-19 vaccination and excess death, there are better ways of statistically showing it.

“Scientists should avoid being right for the wrong reasons,” Rancourt said. “A better approach is to look for temporal associations, which has been done in some detail for Australia.”  (See link for article)

Also, please see:  https://madisonarealymesupportgroup.com/2024/08/15/study-of-125-countries-meta-analysis-on-covid-shots/  The shots are worthless but dangerous.

______________

https://slaynews.com/news/top-study-links-covid-shots-surge-organ-damage-among-children/

Top Study Links Covid Shots to Surge in Organ Damage among Children

Frank Bergman

A team of leading scientific researchers in Germany has just issued a warning to the public after finding direct links between Covid mRNA shots and vital organ damage among children.

Specifically, the researchers found that Pfizer’s mRNA injection is responsible for skyrocketing cases of Immunoglobulin G4-related disease (IgG4-RD) in children aged 5 to 11 years old.

IgG4-RD is a condition that causes inflammation inside the body and damages internal organs, according to Oxford University.

It can affect many different organs, meaning people can have wide-ranging symptoms.

The pancreas is most commonly affected, followed by the bile ducts in the liver, the salivary glands, and the kidneys.  (See link for article)

_______________

https://petermcculloughmd.substack.com/p/large-korean-study-recommends-monitoring

Large Korean Study Recommends Monitoring mRNA Vaccinated Patients for Auto-immunity

Modest Risks Identified, but Cumulative Effects with Repeated Boosters are Concerning

 
JUL 27, 2024

By Peter A. McCullough, MD, MPH

Article excerpts:

There is great concern that with continued dosing of mRNA COVID-19 vaccines, the human body is forced to produce not only the foreign and potentially lethal Wuhan Spike protein, but probably about a dozen additional frameshifted proteins as shown by Boros and colleagues. Invariably these peptides induce an immune attack against the human body as they are expressed on cell surfaces and in some cases like Spike protein, trimerize and are circulatory in blood for months after injection.

Now a large study from Korea by Jung et al, suggests there are increased risks for some autoimmune illnesses after at least two mRNA shots, but not nearly as high as the established dangers of vaccine myo-pericarditis or Guillain-Barre Syndrome.  (See link for article)

https://www.jiac-j.com/article/S1341-321X(24)00209-5/abstract

Japanese Study: COVID mRNA Shots “Significantly Associated” With Myocarditis & Pericarditis

Abstract

Background

The association between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) mRNA vaccines and myocarditis/pericarditis in the Japanese population has not been systematically investigated. This study was aimed at clarifying the association between SARS-CoV-2 mRNA vaccines (BNT162b2 and mRNA-1273) and myocarditis/pericarditis as well as influencing factors by using the Japanese Adverse Drug Event Report database.

Methods

Reporting odds ratios (RORs) and 95 % confidence intervals (95 % CIs) for the association between the vaccines and myocarditis/pericarditis were calculated using data from the database (April 2004–December 2023). Age, sex, onset time, and outcomes in symptomatic patients were evaluated.

Results

The total number of reports was 880,999 (myocarditis: 1846; pericarditis: 761). The adverse events associated with the vaccines included myocarditis (919 cases) and pericarditis (321 cases), with the ROR [95 % CIs] being significant for both (myocarditis: 30.51 [27.82–33.45], pericarditis: 21.99 [19.03–25.40]). Furthermore, the ROR [95 % CIs] of BNT162b2 and mRNA-1273 were 15.64 [14.15–17.28] and 54.23 [48.13–61.10], respectively, for myocarditis, and 15.78 [13.52–18.42] and 27.03 [21.58–33.87], respectively, for pericarditis. Furthermore, most cases were ≤30 years or male. The period from vaccination to onset was ≤8 days, corresponding to early failure type based on analysis using the Weibull distribution. Outcomes were recovery or remission for most cases; however, they were severe or caused death in some cases.

Conclusion

In the Japanese population, SARS-CoV-2 mRNA vaccination was significantly associated with the onset of myocarditis/pericarditis. The influencing factors included age of ≤30 years and male. Furthermore, although most adverse events occurred early after vaccination, overall outcomes were good.
 

Scandinavian Study Confirms Pfizer Pushed ‘BAD BATCHES’ of Covid Shots onto Public

by Vibeke Manniche1, Max Schmeling2, Jonathan D. Gilthorpe3 and Peter Riis Hansen4,5,*
 
Medicina 2024, 60(8), 1343; https://doi.org/10.3390/medicina60081343
Submission received: 17 July 2024 / Revised: 13 August 2024 / Accepted: 14 August 2024 / Published: 19 August 2024

Abstract

Background and Objective: An unexpected batch-dependent safety signal for the BNT162b2 mRNA COVID-19 vaccine was recently identified in a nationwide study from Denmark, but the generalizability of this finding is unknown. Therefore, we compared batch-dependent rates of suspected adverse events (SAEs) reported to national authorities in Denmark and Sweden. 
 
Materials and Methods: SAE and vaccine batch data were received from national authorities in Denmark and Sweden, and analyses of heterogeneity in the relationship between numbers of vaccine doses and SAEs per batch were performed, along with comparison of SAE rates and severities for batches that were shared between the two countries. 
 
Results: Significant batch-dependent heterogeneity was found in the number of SAEs per 1000 doses for both countries, with batches associated with high SAE rates detected in the early phase of the vaccination campaign and positive correlations observed between the two countries for the severity of SAEs from vaccine batches that they shared. Mild SAEs predominated in the batches used in the early part of the vaccination roll-out, where markedly higher SAE rates per 1000 doses in Denmark for the batches that were shared between the two countries suggested that a large proportion of these SAEs were under-reported in Sweden. 
 
Conclusions: The batch-dependent safety signal observed in Denmark and now confirmed in Sweden suggests that early commercial batches of BNT162b2 may have differed from those used later on, and these preliminary and hypothesis-generating results warrant further study.
 
They simply couldn’t allow too many people to be maimed and killed early on.  People would have noticed.
 
For more:

Category:

Activism, research, vaccines, Viruses