The CDC Are Not Health Officials; More Like Terrorists, They Are Worried That a Deadly Flesh-Eating Parasite Could Start Being Spread From Pet Dogs to People in the U.S.this Makes Sense. Talking About Anything With the CDC Is Like Trying to Explain a Train Schedule to a Dog. It Might Just Sit There, Seeming to Pay Attention While Lolling Its Tongue and Waving Its Tail. Ultimately, Though, the Ability to Think Coherently Simply Doesn’t Exist. It’s Not to Blame. It’s Merely the Wiring in Its Head. After That, It Will Retreat Into a Corner and Lick Its Own Butt. With the Dog, It’s the Same
“CDC Warns Pet DOGS Could Start Spreading New Deadly Flesh-Eating Parasite to Humans in the US” HNewsWire: Health officials are worried that a deadly flesh-eating parasite could start being spread from pet dogs to people in the US. Leishmaniasis is a parasitic disease carried by sand flies that, until now, had only been detected in the US among people returning from countries where it’s endemic in the Middle East, Asia, Africa and Latin America. Now researchers at the CDC have warned they are detecting the infection – which causes sufferers to erupt in sores – in people with no travel history to those countries, suggesting it’s spreading domestically. Continue reading The same script is playing out over and over again: you and your pets are “spreaders of the disease”, but don’t worry Dr. Peter Hotez and the US military are working to create…
HNewsWire: As the Center for Disease Crimes (CDC) releases their latest data on the rise of flu, COVID, and RSV cases, and as VAIDS sufferers eagerly await their latest KILL SHOT boosters, the cycle of shedding continues among both genetically modified humans and refuseniks. It’s a time of great confusion and concern, with the ongoing PSYOP-19 and seasonal flu madness.There is a curious tendency for the CDC to exaggerate and rebrand what are essentially harmless common colds.
SRH: When Jesus Launched His Public Ministry and Showed Up on the Scene, He Began Curing Everyone. He Advised Others to Also Breach the Law. Jesus Ignored These Restrictions Because He Was Aware That They Were Keeping People From Receiving Healing. No Franklin Graham Evil Get Your mRNA Kill Shot BS HNewsWire: The entire New Testament scriptures teach us a combat lifestyle as we fight against the Satanic new world order. Allegiance to Jesus Christ must take precedence over allegiance to family members. This is not a popular teaching in today’s corporate Christian church, yet the teachings of Jesus recorded in the Bible are extremely clear on this subject, as this passage in Matthew chapter 10 clearly demonstrates. Luke’s gospel contains considerably harsher wording from Jesus: Anyone who comes to me and does not despise his father and mother, wife…
Read MoreModerna’s “disinformation department” partnered with an industry-backed nonprofit, the Public Good Projects (PGP), to monitor and suppress dissenting voices on COVID-19 vaccine policy, according to a new report by investigative journalists Lee Fang and Jack Poulson published Monday in UnHerd.
Over the last year, the “Twitter Files,” two lawsuits against the Biden administration and other investigations have exposed instances of collusion among government, social media and universities to suppress dissenting speech about COVID-19 policies, election fraud allegations and other topics.
This new report sheds light on Moderna’s behind-the-scenes strategy within this new media landscape. It exposes key actors and how they worked to monitor 150 million websites for the purpose of censoring speech that undermines the company’s COVID-19 vaccine narrative and actively shaping public discourse to benefit Moderna’s bottom line.
Great Barrington Declaration co-author and Stanford University professor Dr. Jay Bhattacharya, who was blacklisted by Twitter, praised the new report in a tweet:
FDA Signs Off on Pfizer’s RSV Vaccine, Despite Safety Risk
The FDA Vaccines and Related Biological Products Advisory Committee (VRBPAC) in May discussed Pfizer’s clinical trial data and an analysis published by the FDA. The analysis showed no increase in preterm births in high-income countries and a numerical increase in upper-middle-income countries driven by South Africa.
The FDA’s VRBPAC committee cleared the shot even though four of the 14 committee members, including Dr. Paul Offit, said Pfizer’s data was inadequate to support its safety. Dr. Offit, a pediatrician and recognized expert in virology and immunology, was concerned by GSK’s results because its vaccine was “almost identical” to Pfizer’s.
Dr. Offit said GSK presented its data during a two-day meeting on RSV in Lisbon, and what they found was that, like Pfizer, there was a temporal association in low- and middle-income countries, meaning “there was sort of a several-month period where you had that increase in statistical association with premature births, but not at other times.”
He also questioned why there was “clearly an increased risk” of premature birth in the vaccinated participants and a decrease in the placebo group.
“If GSK has truly abandoned a program on a similar or almost identical vaccine, that is going to hang over this program,” Dr. Offit said.
Dr. Offit further pointed out that although it was “death” during the GSK clinical trial that initially “got everyone’s attention,” it was severe premature births that led to those deaths.
Dr. Hana El Sahly, VRBPAC chairwoman, said the signal showing an increased risk of preterm births associated with Pfizer’s RSV vaccine was “significant” in phases two and three of its clinical trial and “in a very similar product that was given, you know, on another study.”
“So, having said that, is it reason enough to pause? Probably so,” Dr. Sahly said. “I mean, increasing the risk of or having pregnant women have 20% increased risk of premature delivery is not trivial, even if it is late preterm delivery. The fact that we’re putting them into preterm delivery while we’re sitting here debating the matter intellectually is not trivial.”
When the FDA authorized the vaccine, it determined available data was “insufficient to establish or exclude a causal relationship between preterm birth and Pfizer’s ABRYSVO RSV vaccine but limited its use to women who are 32 to 36 weeks pregnant to mitigate the potential risk. The FDA is also requiring Pfizer to perform postmarketing studies to “assess the signal of serious risk of preterm birth.”
The FDA in 2022 also required Pfizer to conduct several post-marketing safety studies assessing potential long-term impacts of myocarditis-a type of heart inflammation associated with Pfizer’s COVID-19 vaccine-as part of its approval process. The data was required to be given to the FDA in December 2022, but the FDA quietly granted Pfizer an extension when it missed its deadline.
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