Author Archive

Microbiologist Tom Grier Passes

https://www.doughertyfuneralduluth.com/obituaries/thomas-grier

Thomas Grier

November 6, 1954 — June 19, 2024
Duluth

Thomas M. Grier passed away unexpectedly on Wednesday June 19, 2024, in his residence. Tom was born in Minneapolis to Rodney Fellows Grier and Anne Bugocki Grier on November 6, 1954. He graduated from Hopkins High School and earned a BS in biology and chemistry and a Master of Science degree from the U of M Duluth. He worked for K-B Toys in Tacoma, WA and Pocatello, ID before moving back to Duluth, MN when he started work as a Pharmaceutical Sales Rep for Wyeth Co. in women’s products. His science background and outgoing personality helped him win sales awards and be successful. In 1995 he was in the hospital with neurological problems when he was diagnosed with Lyme Disease and could no longer work. He would struggle with the effects of Lyme the rest of his life. Tom started working part-time for Barnes and Noble Booksellers, which he enjoyed. He also started the Duluth Lyme support group and started attending national Lyme Disease conferences to learn of the latest research. He self-published a large booklet with the current information about Lyme to help patients understand the disease. This led to him spending countless hours on the phone trying to help people get the appropriate treatment. Tom traveled around the region giving lectures about the latest findings about Lyme and produced several DVD’s including “Lyme on the Brain” and “Endemic Ignorance”. The past few years, he was plagued with pain and weakness from Lumbar Spinal Stenosis which caused a bad fall and severely limited his mobility, along with his diabetes, which caused swelling of his legs. His death was unexpected, and he was happy and cheerful despite his health issues. He is survived by his brother Terry Louis Grier and he was preceded in death by his parents and older sister Sharon (Grier) Tweit. He will be missed.

Visitation will be held on Wednesday July 10th from 2pm until the 3pm Memorial Service in Grace Lutheran Church. 5454 Miller Trunk HWY, Hermantown, MN 55811. A time of sharing will take place after the service in the church. Arrangements by Dougherty Funeral Home. 600 E. 2nd St. Duluth, MN 55805. 218-727-3555.

To send flowers to the family in memory of Thomas Grier, please visit our flower store.

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**Comment**

Tom will be greatly missed.

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Category:

Activism, Lyme, Uncategorized

Five States Sue Pfizer For False Claims, Report Shows Another COVID Shot Risk Factor & the Uncanny Timing of the Rollout

https://karenkingston.substack.com/p/why-are-5-states-suing-pfizer-and

Why Are 5 STATES SUING PFIZER and NOT Moderna?

Pfizer researched and developed their COVID-19 mRNA injections independent of the Operation Warp Speed program while demanding to maintain ownership and control of their human safety data.

KAREN KINGSTON
JUN 19, 2024

June 18, 2024: Yesterday, Attorney General Kris Kobach broke the news that 4 other states will be joining Kansas in suing Pfizer for willfully concealing, suppressing, and/or omitting material evidence regarding the safety and efficacy of their mRNA injections.

Per the lawsuit, the Big pharma giant conspired with individuals from Health & Human Services, the media, universities, social media platforms, and other businesses and organization in order to manipulate the American people into receiving an injection that they would have otherwise declined if Pfizer had accurately disclosed their COVID-19 mRNA clinical data and adverse events reports to the public and US government.

Why Are 5 U.S. States Suing Pfizer and NOT Moderna?

Per this 4-minute video clip, Kobach addresses the unconscionable acts that Pfizer committed and the reason why he and other state Attorneys General are suing Pfizer first, and not Moderna or J&J.  (See link for article and video)

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**Comment**

In short, Pfizer did not participate in the Operation Warp Speed program.  They remained separate to avoid government oversight and to maintain control (and secrecy) of their data reports.  Our government is still guilty of conspiring with them as well as the media by coughing up $1 Billion to promote the shots. This historical lesson shows that the CIA regularly infiltrates the media, but that now it IS the media.  For decades it has planted news stories.

Again, this is not informed consent.  This is propaganda where people are being paid.

Kingston does a great job explaining the intricacies of contracts and how Pfizer has remained separate from government funding, etc.  She questions if five states suing could spell the end of the mRNA injections.  She also recommends contacting your attorney general and state prosecutor’s office to file a similar suit against Pfizer. Texas Attorney General Ken Paxton filed a similar lawsuit against Pfizer last November.

https://www.reuters.com/legal/kansas-accuses-pfizer-misleading-public-about-covid-vaccine-lawsuit-2024-06-17/

Kansas accuses Pfizer of misleading public about COVID vaccine in lawsuit

By 
Article Excerpts:
June 17 (Reuters) – The U.S. state of Kansas on Monday sued Pfizer (PFE.N), opens new tab, accusing the company of misleading the public about its COVID-19 vaccine by hiding risks while making false claims about its effectiveness.
In a lawsuit, opens new tab filed in the District Court of Thomas County, the state said the New York-based drugmaker’s alleged false statements violated the Kansas Consumer Protection Act. It is seeking unspecified money damages……
The lawsuit claims that, beginning shortly after the vaccine’s rollout in early 2021, Pfizer concealed evidence that the shot was linked to pregnancy complications, including miscarriage, as well as inflammation in and around the heart, known as myocarditis and pericarditis.  (See link for article)
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**Comment**
Pfizer has been in trouble for many crimes throughout history, yet doesn’t pay a dime in taxes.  Its own employees have exposed the company’s misdeeds.
Our corrupt public health agencies protect this company, and it’s taken a court of law to even get Pfizer’s trial data, which should be accessible to everyone.
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BREAKING Publication: COVID-19 Vaccines: A Risk Factor for Cerebral Thrombotic Syndromes

Unacceptable Hazard for Blood Clots to the Brain

JUN 19, 2024
By Peter A. McCullough, MD, MPH

I have several patients who have suffered multiple strokes after COVID-19 vaccination. The Spike protein is known to circulate in blood as shown by Brogna et al in half of vaccinated patients for at least six months. Other studies have demonstrated the Spike protein directly damages the wall of the blood vessels and causes blood clots.

Rogers et al use the CDC Vaccine Adverse Event Reporting System to compare rates of cerebral thrombosis among COVID-19 vaccine recipients to the large number of individuals who take an influenza vaccine annually. The vast majority of events reported to VAERS are made by doctors and other healthcare providers who have determined the vaccine is the cause of the problem. Compared to influenza vaccines given over 34 years, COVID-19 vaccines in 36 months of use had over 1000-fold increased risk of most blood clot events, and compared to all vaccines combined administered over 34 years, this risk remained at over 200-times greater with COVID-19 vaccination.

This paper did not capture the level of permanent neurologic devastation and disability suffered by these patients. I can tell you that the rates must be very high given the extensive nature of the blood clots reported. These data among others strongly support removing all COVID-19 vaccines and boosters from the market. No one should be put at risk for a serious stroke with any vaccine.  (See link for article)

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https://www.dossier.today/p/pfizer-pro-quo-more-evidence-emerges?

Pfizer Pro Quo: more evidence emerges that drugmakers cut deal to help Biden win election

Another quid pro quo for quid pro Joe?

JORDAN SCHACHTEL
JUN 19, 2024
Article Excerpts:

Anthony Fauci’s new book has granted the public more detail concerning the truly impeccable timing of Pfizer’s mRNA Covid-19 vaccine trial data rollout.

We already know that Pfizer decided to inexplicably delay publishing the results of their mRNA trial from October 2020 to right after the election….

The original deal with Pfizer was negotiated by the Trump Administration during the days of Operation Warp Speed. It paid the pharma giant $19.50 a dose. The Biden Administration would eventually sign off on a deal to give Pfizer approximately $30.48 per dose, resulting in an astronomical 56+% hike from the deal negotiated by the Trump administration.

At the peak of Covid hysteria, Pfizer was bringing in almost $10 billion in net income per quarter, thanks to a 33% mRNA profit margin in the U.S. market.  (See link for article).  

http://

Comedians Finally Get It.  When Will Everyone Else?

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Category:

Activism, vaccines, Viruses

Plum Island History

http://  Approx. 12 Min

Why New York’s Plum Island is Totally Forbidden

3/24

Plum Island, located off the coast of Long Island, has a rich history spanning centuries. Originally known as “Isle des Plumes” by early French settlers due to its abundant bird population, it later became a haven for pirates and smugglers during the colonial era. In the 19th century, it was used as a quarantine station for diseased livestock, helping prevent the spread of diseases to mainland farms. During World War II, the island was taken over by the U.S. government and used for military purposes. In 1954, the Plum Island Animal Disease Center was established by the U.S. Department of Agriculture, where research on infectious animal diseases, including foot-and-mouth disease, was conducted. Today, the island remains a site of scientific research, though its future is uncertain amidst discussions of potential closure and redevelopment.

The video explains that as of 2023 the island was slated for closure and to be sold at private auction, while the facility itself would move to Kansas City University. As a part of the Consolidated Appropriations Act of 2021, and the response to the most recent ‘pandemic’ outbreak, the island was offered to federal agencies first. As of Feb. 2024, the facility still operates at Plum Island.

While the author of the video emphasizes the safety of the lab, the book Lab 257 paints quite a different picture with virus outbreaks, infected workers, flushing of contaminated raw sewage into area waters and the insidious connections between the island and Lyme disease and West Nile Virus.

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Category:

Activism, Lyme, research, Ticks

Ross Lyme & Tick-borne Diseases Protocol Version 4

https://www.treatlyme.net/lyme-disease-treatment-guidelines

About The Ross Lyme & Tick-borne Diseases Protocol—Version 4

New in Version 4

The Ross Lyme & Tick-borne Diseases Protocol–Version 4 update, released 6/17/24, has a number of significant changes.

Name change. In Version 4, I have updated our name to include “tick-borne”. This recognizes that people can have Bartonella, Babesia, or other tick-borne diseases, separate from having Lyme (Borrelia) infection.

But there are more significant updates than our name change. Version 4

  • Emphasizes plant-based foods recommendations in Part 2. Diet;
  • Promotes healthy intestinal microbiome—even on antibiotics with a new Part 3. Healthy Intestinal Microbiome; and
  • Includes an herbal antibiotic only option to treat the three Bs (Borrelia, Bartonella, and Babesia) simultaneously in Part 12. Lyme Infection and Part 13. Bartonella & Babesia Infections.
  • Moves lifestyle, and related areas, of sleep, diet, healthy intestinal microbiome, and exercise to the front of the protocol to emphasize the key role these areas have in recovery.

Introduction

These are support and treatment guidelines to treat chronic Lyme or tick-borne infections. This protocol addresses most problems that keep a person from getting well. It is more comprehensive than the antibiotic focused Infectious Disease Society of America (IDSA), International Lyme and Associated Disease Society (ILADS), and United States Centers for Disease Control and Prevention guidelines. While herbal and prescription antibiotics may decrease the germ load in chronic Lyme and tick-borne infections, they often do not correct the underlying problems that cause ongoing symptoms.

The Ross Lyme Support Protocol includes essential steps for the beginning and throughout a chronic Lyme disease or tick-borne infection treatment. It is designed to:

  • boost the immune system,
  • improve detoxification,
  • speed recovery,
  • kill the infections, and
  • protect and repair from the harmful effects of the infections and the herbal or prescription antibiotics.

While the following Lyme disease and tick-borne infection treatment approach focuses on a limited number of areas, it may correct most of the problems like:

  • low energy,
  • pain,
  • insomnia,
  • brain, neurologic, and thinking problems (brain fog), and
  • immune compromise and suppression.

Herxheimer Reactions. When a person starts a Lyme disease or tick-borne infection treatment or changes herbal and prescription antibiotics, it is common to experience some worsening in symptoms. See Herxheimer Die-off Reaction: Inflammation Run Amok for more information about this and the steps you can take to treat it.

Treatment Length and Persistence. Generally, it takes a minimum of six months to see if these supports and treatments will help. Supplements can speed recovery, but treating Lyme still takes time. Once you have marked improvement, then you can likely stop many of these nutritional supports except for probiotics, curcumin, ashwagandha, and a good multivitamin. See Getting Healthy: Will I? When? How Do I? for more information about Lyme disease and tick-borne infection treatment length and persistence.

About Supplements. Throughout this protocol I include supplements as nutritional supports based on their known functions. Basic research and my clinical experience show they may help the various symptoms and problems in Lyme disease and tick-borne infections.  (See link for article)

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**Comment**

Lots of great info here.

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Category:

Babesia, Bartonella, Detoxing, diet and nutrition, Lyme, Pain Management, Sleep, Supplements, Treatment

The FDA is a Front Organization

**UPDATE**

See: The FDA’s War Against America’s Health

Illustrating the fact the FDA is completely and hopelessly bought out, it is now advocating for a 10th COVID gene therapy injection that doesn’t stop transmission, illness, or death.

When will someone notice the emperor has no clothes on?

https://bailiwicknews.substack.com/p/on-fda-buildings-as-virtual-mailboxes

On FDA buildings as virtual mailboxes to project the public illusion of biological product manufacturing regulation.

Part 9 of series.

 
KATHERINE WATT
MAY 25, 2024
 

A Bailiwick reader is doing a deep research dive into pre-1972 statutory and regulatory history of some Public Health Service-Health and Human Services divisions, including National Institutes of Health (NIH) and Food and Drug Administration (FDA).

For context, 1972 is the year that ostensible biologics regulation — which is actually non-regulation — transferred from the NIH Division of Biologics Standards to the FDA Bureau of Biologics.

November 1973 is when FDA published a consolidated set of biological product manufacturing non-regulations in the Federal Register.

Administrative rule-making by FDA since 1973 is relatively easy to locate.

Administrative rule-making by NIH prior to 1973 is more difficult to locate.

One of the questions the reader is trying to answer has to do with whether biological regulation authority was ever statutorily established by Congress, for NIH and its precursor organizations, going back to the late 1800s.

Modern-day NIH and FDA officials present historical accounts of how the biological product and vaccine manufacturing regulatory systems began and developed.

But from her research so far, the reader has concluded that their origin-story claims are not supported by the text of the statutes they cite.  (See link for article)

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Important quote:

Since the advent of electronic filing systems, the application and licensing forms have been filed, transferred and stored electronically, and deleted at regular intervals.

There are no technicians in the buildings, there’s no equipment, no sample testing occurs.

It’s all a front: statutes, regulations, procedures, application forms, buildings, addresses, offices, labs, approved applications and licenses sent by FDA back to the factories, everything.

A handful of people at pharma companies know it.

A handful of people at FDA know it.

Go to top link not only for the full article but for the 8 prior parts.  Watt has done a lot of legwork and it deserves to be shared widely.  Things, once again, are not as they seem.  The FDA like the UN, WHO, and WEF should be disbanded.  These organizations are out of control and do ZERO to protect public health.  They all protect their own vested interests.

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Category:

Activism, Supplements, vaccines