DeSantis Announces Major Move Against COVID Vaccine Makers
Florida Republican Governor Ron DeSantis announced on Tuesday that he was seeking a grand jury investigation into the way COVID-19 vaccines were marketed and promoted and whether wrongdoing occurred.
"It is against the law to mislead and to misrepresent, particularly when you're talking about the efficacy of a drug," DeSantis said on Tuesday.
"Just recently, Florida got $3.2 billion through legal action against those responsible for the opioid crisis," he noted of previous legal action to hold drugmakers and drug sellers accountable. "It's not like this is something that is unprecedented," DeSantis said of his efforts to probe COVID-19 vaccines and the way they were presented to Floridians.
"Today, I'm announcing a petition with the Supreme Court of Florida to impanel a statewide grand jury to investigate any and all wrongdoing in Florida with respect to COVID-19 vaccines," DeSantis said.
"We anticipate that we will get the approval for that," DeSantis explained of his petition. The grand jury, DeSantis expects, "will be something that will be impaneled mostly likely in the Tampa Bay area."
DeSantis added that the grand jury "will come with legal processes that will be able to get more information" about any wrongdoing, and will "bring legal accountability for those who committed misconduct," he said.
The announcement on Tuesday is a follow-through on a promise Governor DeSantis made earlier in December when he pledged that his administration would "work to hold these manufacturers accountable for this mRNA [vaccine] because they said there was no side effects and we know that there have been a lot," DeSantis said of his plan to "bring some accountability" for COVID-19 vaccine makers, namely Pfizer and Moderna who produced the mRNA vaccines.
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Top Doctor: Long COVID is Being Exaggerated to Extort Taxpayers
John's Hopkins Medical School Professor Dr. Marty Makary, who also serves as a health advisor for Virginia Governor Glenn Youngkin, is warning "long COVID" is being exaggerated in order to extort American taxpayers for more money.
"Long Covid is real. I have reliable patients who describe lingering symptoms after Covid infection. But public-health officials have massively exaggerated long Covid to scare low-risk Americans as our government gives more than $1 billion to a long Covid medical-industrial complex," Makary writes in the Wall Street Journal.
"The National Institutes for Health has been intensely focused on studying long Covid, spending nearly $1.2 billion on the condition. To date, the return on investment has been zero for the people suffering with it. But it’s been terrific for MRI centers, lab testing companies and hospitals that set up long Covid clinics," he continues. "I’ve talked to the staff at some of these clinics and it’s unclear what they are actually offering to people beyond a myriad of tests."
The White House continues to demand endless funding as Dr. Anthony Fauci claims the U.S. is still "in the middle" of a pandemic.
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Michigan Medicine Prof. of Biologic Nanotechnology investigates Adverse Reactions Associated with COVID-19 mRNA Vaccines
The founding Director of the Mary H. Weiser Food Allergy Center, and Ruth Dow Doan Professor at Michigan Medicine not to mention an exceptional allergy and clinical immunology specialist, Dr. James Baker Jr., spearheads a 200-patient interventional study titled “Assessing Safety of COVID-19 mRNA Vaccine Administration in the Setting of a Previous Adverse Reaction.” Launched in the spring, this single-group assignment open-label study runs till December 2024. In the study, the participant receives a dose of Pfizer-BioNTech (Comirnaty) or Moderna (Spikevax), both mRNA COVID-19 vaccines. The goal? Determine primary and secondary endpoints associated with safety of the mRNA-based vaccines. Specifically, the study team hypothesizes that the individuals that have had adverse reactions to a dose of an mRNA COVID-19 vaccine will tolerate an additional dose and those with a personal history of allergic reaction will tolerate vaccination with an mRNA COVID-19 vaccine.
While the U.S. Food and Drug Administration (FDA) has deemed the mRNA COVID-19 vaccines safe and effective, various side effects and adverse events have been identified, including in the regulatory package insert. For example, a cardiovascular signal has been identified in the form of myocarditis and pericarditis in young persons.
Can persons that had an adverse reaction to the first or second dose of either mRNA -based COVID-19 vaccine (Pfizer-BioNTech or Moderna) safely tolerate an additional dose if they have a personal history of allergic reaction who declined COVID-19 vaccination administration can safely tolerate an initial dose?
In this study funded by both the University of Michigan and the Wallace Foundation, Dr. Baker along with Dr. Charles Schuler IV, seek 200 eligible to receive an initial or additional dose of either Comirnaty or Spikevax.
Participants in this study will also be required to have 1-2 in person visits along with phone call follow up visits.
The study hypothesizes that individuals that have had adverse reactions to a dose of an mRNA COVID-19 vaccine will tolerate an additional dose, and those with a personal history of allergic reaction will tolerate vaccination with an mRNA COVID-19 vaccine.
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Pathological Syncytia Formation with mRNA Vaccines
One of the curious findings from the original randomized trials of mRNA vaccines was an explosive rate of early infection after the first injection as compared with placebo. In a recent paper from Sfera et al., the description of pathological syncytia or fusion between immune cells is described: “The LNP technology, to put it simply, mimics viral envelopes with externalized phosphatidylserine (ePS), a universal “eat me” signal, that directs immune cells to engulf the particle.
However, as ePS is also a potential “fuse me” signal, LNP may inadvertently facilitate the formation of pathological syncytia. Moreover, ePS may activate a disintegrin and metalloprotease 10 and 17 (ADAM10) (ADAM 17), master regulators of syncytia formation, contributing further to the unintended consequence of cell-cell fusion…As mRNA vaccines are based on pre-fusion epitopes, the fusion pathology may be undeterred, allowing viral infection by syncytia formation to continue unabated.
This is significant, as it could account for the reoccurrence of COVID-19 symptoms in fully vaccinated individuals. The authors point out that SARS-CoV-2 utilizes more than just the ACE2 receptor to gain entry into the fused cells and by overlooking this possibility, vaccine developers have made a blunder.
This is further complicated by the choice of lipid nanoparticles and polyethylene glycol which facilitate entry into organs were syncytia as well as Spike protein will incite inflammation and immune system regulation. Sfera also considers pregnancy: “Several studies demonstrated that SARS-CoV-2 can activate HERV-W, an ancestral gene that encodes for the physiological placental fusogen syncytin-1 responsible for the merger of trophoblasts during the early pregnancy. This suggests that the reproductive post-vaccine events may be triggered by the furin cleavage site pathology.” Such processes could occur in the gravid uterus and compound the bleeding and clotting risks of ill-advised vaccination is this special population.
In summary Sfera et al. point out the following blind spots of well-funded DARPA consultants, BARDA funded academic researchers, and later, by Pfizer and Moderna in mRNA vaccine development: 1) pathologic syncytia formation, 2) use of lipid nanoparticles with PEG, 3) failure to consider SARS-CoV-2 could use alternative points of cell entry other than ACE2 (metalloprotease pathway, antibody dependent enhancement, cell penetrating peptides, viroporins).
With billions of people rushed into indiscriminate mRNA vaccination, virologists and immunologists will be picking up the pieces of a failed vaccine campaign that has left so many at risk for more SARS-CoV-2 infections and progressive complications over the months and years to come.
https://www.trialsitenews.com/a/pathological-syncytia-formation-with-mrna-vaccines-482b8930
**************************************************Also see my other blogs. Main ones below:
http://edwatch.blogspot.com (EDUCATION WATCH)
http://antigreen.blogspot.com (GREENIE WATCH)
http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH) Also here
http://australian-politics.blogspot.com (AUSTRALIAN POLITICS)
http://snorphty.blogspot.com (TONGUE-TIED)
https://immigwatch.blogspot.com (IMMIGRATION WATCH) Also here
https://awesternheart.blogspot.com (THE PSYCHOLOGIST)
http://jonjayray.com/blogall.html More blogs
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