Archive for the ‘Activism’ Category

Shocking New COVID Shot Side Effects

https://thehighwire.com/videos/shocking-new-covid-vaccine-side-effects/ Video Here (Approx. 13 Min)

Welcome to the next generation of “vaccine” harms being reported. From mouth blisters to debilitating nervous system disorders, scientists are continuing to report troubling side effects from COVID-19 vaccines.

POSTED: March 25, 2022

Hour long video of adverse events after COVID shots. People dropping and spasming uncontrollably.

Another 20 Minute compilation of athletes, reporters, musicians and others collapsing after shots.

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Category:

Activism, vaccines, Viruses

Researcher Blows Whistle on Data Integrity Issues in Pfizer’s COVID Shot Trial

**UPDATE April, 2022**

As they say: “Follow the money”.

More and more is trickling out about Pfizer including whistleblowers stating the shot is a bioweapon, data was falsified, internal emails tried to cover up fetal cell usage, that it copies the mRNA spike protein into human DNA, has caused increased COVID in young kids, and the suspicious coincidence that the 2022 Oscars were sponsored by Pfizer, the company that just happens to have a new Alopecia drug coming out very soon, and the Rock/Smith distraction. Seems everything today is “brought to you by Pfizer.”

https://thevaccinereaction.org/2022/03/researcher-blows-whistle-on-data-integrity-issues-in-pfizers-covid-vaccine-trial/

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Researcher Blows Whistle on Data Integrity: Pfizer COVID shot

Brook Johnson was fired for exposing problems with the integrity of Pfizer’s trial data

For researchers who were testing Pfizer’s vaccine at several sites in Texas during that autumn, speed may have come at the cost of data integrity and patient safety. A regional director who was employed at the research organization Ventavia Research Group has told The BMJ that the company falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial. Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding. After repeatedly notifying Ventavia of these problems, the regional director, Brook Jackson , emailed a complaint to the US Food and Drug Administration (FDA). Jackson has provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails.

My name is Brook Johnson. I was fired in September of 2020 for being a whistleblower. I was working on Pfizer’s phase III […] trial on their COVID-19 vaccine. My first day on the job was the 8th of September, and from the very beginning I noticed irregularities, things that were questionable. I would bring up the concerns to my managers and it was always… ‘We’re understaffed, we’re really trying hard to make this work.’ At one point, when I was going through e-mails, there were e-mails from ICON begging Ventavia to follow up on severe adverse events that had been reported. There were several e-mails about mislabeled specimens—blood specimens—and nasal swabs.

Read the full investigation: Covid-19: Researcher blows the whistle on data integrity issues in Pfizer’s vaccine trial https://www.bmj.com/content/375/bmj.n…

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Category:

Activism, vaccines, Viruses

2 Minutes of Truth on COVID Shots – Dr. Zelenko & Steve Kirsch

https://rumble.com/vy8swt-premeditated-mass-murder-evidence-suggests-the-fda-and-pfizer-were-aware-of  Video Here (Approx. 2  Min)

“Premeditated Mass Murder” Evidence Suggests FDA & Pfizer Completely Aware of What Would Happen

Dr. Zelenko presents leaked FDA information on mRNA shots.

The FDA had a leaked internal presentation detailing severe side effects two months prior to “vaccine” rollout and Pfizer’s data correlates with the FDA’s.

“There’s a term for this: when there’s 100% correlation. What, the FDA has prophetic powers? So let me tell you what it is: it’s first-degree premeditated mass murder, crimes against humanity, and genocide.” ~ Dr. Zelenko

COVID shots are linked to:

https://mobile.twitter.com/lakovosjustice/status/1507554765106028550  Video Here (Approx. 2 Min)

Steve Kirsch Speaks at U.S. Senate Hearing

U.S. Senate expert witness testimony states that there are 410,000 unexplained deaths in Americans. Insurance company data shows 40% increase in deaths of people under 64. This is the greatest killer of mankind. This is the worse coverup in human history.

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The correlation to the COVID-19 shots now is irrefutable, just from using the U.S. Government’s own data from the CDC, and also from the Vaccine Adverse Events Reporting System (VAERS).

Category:

Activism, vaccines, Viruses

Growing Evidence of Lyme-Like Illness in Australia

Growing Evidence of an Emerging Tick-borne Disease That Causes a Lyme-like Illness For Many Australia Patients

Professor Noel. Campbell
Fellow Australasian College of Nutritional and Environmental Medicine

sub1281_Campbell (1)  372 page Paper Here

Executive Summary:  

Over the past three decades, thousands of Australian families have felt the impact of Lyme and  other tick-borne diseases (TBDs), with an estimated 10,000 individuals affected each year. Whether  it is a laborer who cannot continue his work because of debilitating joint pain, or a child who  misses school because of debilitating fatigue, pain and cognitive dysfunction, TBDs can have a  significant effect on the day to day lives of Australians. Since Lyme disease was first identified in  Australia in 1982, the disease has spread geographically, and in severity. It has been documented  that there has been an increase in tickborne diseases in Australia, including early and late forms, as  well as an increase in neurological cases.

The patient experience may be characterized by delays in diagnosis, confusion, frustration,  ongoing illness, with, in many cases poor outcomes, disability and a significant financial burden.  (Most recently, we have started to record deaths in Australia from tickborne diseases.)

Recognizing these facts, the Parliament of Australia has referred these matters to the Senate  Community Affairs References committee for enquiry and report. The Senate acknowledged the significant toll TBDs may exact on individuals, families, communities, and the state, noting that  TBDs pose a serious threat to the health and quality of life of many residents and visitors to  Australia.

The purpose of this inquiry should be to establish a Lyme and related tickborne diseases task force charged with exploring and identifying recommendations related to education and awareness, long term effects of misdiagnosis, prevention, and surveillance. The intent of the recommendations are  generally to improve Australia’s response to the tickborne disease burden.

This submission reflects the history of TBDs in Australia, and includes specific recommendations as well as implementation strategies, case studies, and resource needs. While the Senate Inquiry  will be the result of months of research and co-collaboration, it is clear that its report is merely the  beginning of a much-needed dialogue and structured planning process across the country.

The primary recommendations in this submission focus on increased and improve surveillance,  prevention of tick exposure strategies and tactics, as well as education and awareness for  healthcare practitioners(HCPs), patients, the general public and other stakeholders.

In contemplating each recommendation, the author carefully considered each of the countries key  stakeholders, including patients of all ages and their families, vulnerable populations, health care  providers, domestic animals, researchers, Government agencies, policy makers, schools and  community organisations, and the general public.

Key Themes: 

  1. Tickborne disease knowledge and research is evolving rapidly. It will be vital to encourage  critical research, to understand the scope and scale of Lyme and other TBDs in Australia,  and to develop options to improve the public health response and the community/ patient  outcomes.
  2. Different schools of thought exist among all stakeholders regarding Lyme. Ambiguities do  exist so it is important to promote a strong and academically rigourous pursuit of better  research to help clarify the best options for patients. We are encouraged to keep an open  mind, and to continue to explore the nature of these diseases and their health impacts.
  3. The most critical research gap is the lack of a gold standard test for Lyme and other  tickborne infections; a test that can quickly and accurately diagnose the disease, and prove  or disprove ongoing persistence. Research into bio- resonance for diagnosis and treatment of Lyme disease is producing encouraging results in Melbourne Australia.
  1. Without more research and surveillance, it will be difficult to stay ahead of this rapidly  evolving public health problem.
  2. The cost to Australia of doing nothing is considerable.
  3. Without targeted and significant funding, it is unlikely these recommendations can be  deployed in an effective and impactful way.
  4. Collaboration among the commonwealth’s diverse stakeholders Will help ensure programs  and strategies are innovative, effective, and measurable.  Too many Australians have suffered the consequences of Lyme and TBD’s, and without action,  thousands more remain at risk. This is important public health challenge affects all Australians  -every state has reported ticks infected with bacteria. And yet our children, our elderly, and our immunocompromised are most at risk and most vulnerable to their impact. Our actions now,  will significantly impact Australian youth’s risk and future potential.The author respectfully requests Swift action on the enclose recommendations by all state  leaders charged with ensuring the protection and well being of the Commonwealth’s residents.

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Category:

Activism, Lyme, research, Testing, Ticks

Screenwriter Turns a Couple’s Courageous Lyme Fight into a Film Script

https://www.lymedisease.org/doherty-courageous-lyme-fight/

Screenwriter turns a couple’s courageous Lyme fight into a film script

By Steve Doherty

March 15, 2022

I was bitten on the neck by a tick in 1996, while camping in southern Mississippi. But I didn’t notice or remove the tick until five days after I returned home.

Looking back, I now recognize the subtle symptoms in the years following, such as hand rashes, crackling in my neck and mild cardiac arrhythmias.

In 2010, I became very ill. I spent a year and a half visiting physicians with no definitive diagnosis.

The symptoms had intensified to include numbness in my hands and feet, increased cardiac arrhythmias, consistent tinnitus and severe fatigue. Finally, an ILADS-affiliated doctor diagnosed me with Lyme in 2012.

I had worked as a respiratory therapy for 39 years, but could do so no longer due to my symptoms. I retired and began to delve into another love, screenwriting.

The Lasiter Family

Through a number of incredible circumstances, I became acquainted with Jessica and Lance Lasiter. Jessica is 30 years old and suffers highly debilitating symptoms. She became ill in 2010 and like me, experienced misdiagnosis and questioning of her symptoms.

At one point, doctors told her she had ALS. But eventually, she discovered she had neurological Lyme. Jessica is presently wheelchair-bound with very little use of her hands and much difficulty speaking.

Writing with one functional finger

Jessica and Lance are a courageous couple. Jessica, in her determination to help others, has even written the manuscript for a book based on her journey, using her one functional finger, on her cell phone. She transfers her work to her laptop, which she operates with a foot mouse.

Getting to know Jessica and Lance motivated me to write a screenplay based on their journey. Jessica, Lance and I met on a weekly basis for two years in order that I could learn their story, with its many ups and downs.

Their story was recently chronicled in The Clarion Herald, a local New Orleans newspaper. Here is a link to that article.

We now have a completed script, synopsis and log line for the project. We feel that it is a story that will truly encourage others, as well as inform many regarding the seriousness and horror of Lyme disease. The story is also one of Jessica’s courage and determination to help others in the face of severe adversity. The film project is currently titled, “The Cub & The Raider.”

We expect Jessica’s book manuscript, “We’ve Only Just Begun,” to be ready for publication soon.

During my work with Jessica and Lance, I have witnessed a devotion of a couple to each other that one rarely sees. They love each other unconditionally. This inspires me to use my situation and understanding of Lyme to put forth this story. By virtue of this I am determined, more than ever, in spite of the continued symptoms that I experience, to press on to completion. I hope it will help many people cope with their own Lyme disease challenges.

Steve Doherty lives in Metrairie, Louisiana. For more information regarding the book and film projects, he can be contacted at brownpelican08@aol.com.

Category:

Activism, Lyme