Sunday August 20 Mega-Event: “Have You Stopped Trusting Yet?” With Funeral Director John O’Looney, Dr. Mike Yeadon, Sasha Latypova, and Dr. Meryl Nass MD
Please join this eye-opening zoom conference and invite your friends!
BS”D
G-d willing, this Sunday August 20, starting at 1:00 PM Eastern Time!
Have you stopped trusting yet?
Governments and medical organizations pushed the covid shots with a vengeance.
What did they really know at the time?
Where did the shots come from?
What has been the deadly aftermath?
And, what are they up to next?
Sunday August 20 @ 1 PM EASTERN TIME
Funeral Director John O’Looney: As the covid vaccines claim ever more lives, have we learned anything?
Dr. Mike Yeadon PhD: What their endgame is & how I knew their narrative was false
Sasha Latypova: Militarized Healthcare
Dr. Meryl Nass MD: New RSV shots killed 12 babies in trial - now CDC approved for every newborn - JUST SAY NO! Plus much more.
Join by Zoom: https://us02web.zoom.us/j/9521753151?pwd=QnhXdmJ3Q2FFV202K1RvSGpkK0ZvQT09
Or: tinyurl.com/TruthSavesLives
Meeting ID 952 175 3151
Passcode 1818
Or call: 929-205-6099 and enter above meeting ID and passcode
For event recording please go to truth613.substack.com or call the JAVI hotline: (929) 277-2700
the other day I slapped a link or two on some substacks about the biolab in Reedley Ca ….. with little to no response. While comparing various articles written over about a two week period some things bothered me about the ‘response’ by the 3 letter agencies. One article stated the Feds told the local Fresno Co personnel to suppress the information….. this lab was discovered in Dec 2022 and did not hit the press for almost 6 months…. Another issue I have is initial reports stated in the same warehouse where this occurred PCR tests were being manufactured or were present where at least a dozen pathogens and live mice were present. The FDA did a recall on the ‘PCR’ tests (see attached) which advised people to return them to the same company that distributed them. As a retired cop, this makes no f@#&$ing sense. Those test should be tested for the pathogens which were present in the warehouse.
https://www.fresnobee.com/news/local/article278262808.html
https://www.fda.gov/medical-devices/medical-device-recalls/sml-distribution-llc-recalls-skippack-medical-lab-covid-19-direct-antigen-rapid-tests-are-not
While we’re at it
In the summer of 2018, one of China’s largest domestic vaccine makers sold at least 250,000 substandard doses of vaccine for diphtheria, tetanus, and whooping cough. It was the latest in a slew of scandals caused by poor quality drug products made in China over the last decade. In 2008, the contamination of a raw ingredient imported from China and used to make heparin, a blood-thinning drug, was associated with at least eighty-one deaths the United States.
In 2008, the contamination of a raw ingredient imported from China and used to make heparin, a blood-thinning drug, was associated with at least eighty-one deaths the United States. According to an investigative journalist, fraud and manipulation of quality data is still endemic in Chinese pharmaceutical firms.
Here's an alert which you can possibly bring to the attention of others at this meeting. Is appropriate for Meryl Nass' portion of the program. A trial balloon for putting a drug into the classification of "vaccine" in order to receive the liability shield and as well to get it on the childhood vaxx schedule therefore guaranteeing uptake for Pharma Cos. and obtain free taxpayer subsidies.
Classic Pharma playbook.
Vote to Add Drug to Childhood Vaccination Schedule Opens Door to Daycare Mandates, Tracking, and Injury Liability Shield
Despite clear statements and acknowledgments by federal officials and several committee members at last week’s Advisory Committee for Immunization Practices (ACIP) meeting that nirsevimab is not a vaccine, this U.S. Food and Drug Administration (FDA) approved drug will essentially be treated as a vaccine by the U.S. Centers for Disease Control (CDC).
This action is due to the CDC committee’s determination that “vaccine” is not well defined in federal statute. Therefore, the new drug manufactured by Sanofi and Astra Zeneca is eligible for inclusion in the federally recommended childhood vaccination schedule and in the federally funded Vaccines for Children Program (VFC).
The ACIP vote to treat the new genetically engineered RSV drug as a vaccine for the purpose of adding it to the recommended childhood vaccination schedule, opens the door to adding the fake vaccine to state mandates for daycare attendance and giving Sanofi and Astra Zeneca a liability shield from vaccine injury lawsuits by adding it to the federal Vaccine Injury Compensation Program (VICP).
......
Nirsevimab is a genetically engineered monoclonal antibody designed to passively provide immunity to RSV and was approved by the FDA for licensure as a drug under the trade name Beyfortus on July 17, 2023.8 9 The basis for licensure was in part the recommendation from the FDA’s Antimicrobial Drugs Advisory Committee (AMDAC), which evaluates data on drug products for use in treating infectious diseases and disorders,10 11 12 rather than the FDA’s Vaccines & Related Biological Products Advisory Committee (VRBPAC), which evaluates scientific evidence for the safety and efficacy of new vaccines, which and has made no such recommendation.
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The addition of nirsevimab to the VFC program is likely partly due to its private sector price tag of $495/dose. However, the VFC designation only reduces that cost to $395/dose and was criticized by committee members as too costly.
The VFC’s funding comes through an entitlement program under Section 1928 of the Social Security Act.19 Vaccines administered through the VFC program are at no cost to the child, but are not “free” because VFC funding comes from federal tax dollars and by law each state is required to participate through Medicaid.
More here:
https://www.nvic.org/newsletter/aug-2023/nirsevimab-acip-vote-treated-like-vaccine