Vaxers? FR Vaxers please answer the phone.
PING
...that don't work. Brandon goes first?
Meanwhile our current vaccines are basically worthless as per the Pfizer CEO!
Pfizer CEO: Our Vaccines Offer ‘Limited, If Any Protection’
townhall.com ^ | 1/11/2022 0900 hrs et | Katie Pavlich
Posted on 1/11/2022, 10:03:58 AM by rktman
Speaking during remarks to a J.P. Morgan healthcare conference this week, Pfizer CEO Albert Bourla openly stated current vaccines the company developed for Wuhan coronavirus offer “limited, if any” protection against contracting current variants of the disease. He then encouraged booster shots.
The statement from Bourla comes as the Biden administration continues to justify vaccine mandates for federal workers, contractors and private businesses. The Supreme Court heard arguments about President Biden’s mandates for private companies and medical workers last week. A ruling is expected soon on the constitutionality of the mandates.
A number of people who have pointed out the waning efficacy of Pfizer’s vaccines, which Bourla touted last year as being “100 percent” effective against contracting or transmitting the virus, have been banned by social media companies.
(Excerpt) Read more at townhall.com …
Bait-and-switch is a crime.
Every time they hit you with a booster, your immune system gets weaker. It’s called AIDS.
In other news, CEO of McDonald’s says that 1 Big Mac a week isn’t enough, you should eat at least 2.
SURELY I’m not the only one seeing this cash grab for what it is?
Thanks again for your meticulous research and for links to all those studies.
Rand Paul has sure got Fauci’s number. He is exposing that miserable fraud day by day.
This post combined with this post pretty much tell you he should stick to treating transgender monkeys:
Pfizer CEO: Our Vaccines Offer ‘Limited, If Any Protection’
https://freerepublic.com/focus/f-news/4028574/posts
Please watch this short video about what is REALLY going on. It really is worse than you could ever imagine. Fauci and the dems have destroyed us.
https://www.bitchute.com/video/LukPaRDJHysl/
FDA and Pfitzer need to give up the ghost and admit their vaccine is substandard to J&J and Moderna and should be withdrawn
I can imagine them slapping some new labels on the vials of death juice.
p
Ivermectin is your friend.
******************************************
The Governement and Public Health Physicians mislead America:
1) mRNA vaccines DO NOT provide immunity of any kind.No antibodies.
2) mRNA vaccines do not prevent transmisson of the virus.
3) mRNA vaccines do attenuate Covid symptoms if the Covid mutant variant is vulnerable, for a limited period of 5 months ( Pfizer) to 6 or 8 months ( Moderna).
4) The mRNA vaccines do not work in the nasal cavity, in the pharnyx or in the lung, they only work in the blood stream, but give no protection to Covid involved organs.IVM does.
Thats why Ivermectin in your friend when taken within a few days of the infection or as prophylaxis.
Proof of Effectiveness of Ivermectin:
***************************************
How Ivermectin works:
There is reasonably solid evidence that ivermectin docks to the spike protein itself to prevent binding to the ACE2 receptor which is the primary pathology causing the tissue damage and clots related to SARS-CoV-2. Therefore, this is also an implication that this ability of ivermectin to disable the binding of the Spike protein including the vaccine-produced spike proteins. This binding of ivermectin to disable the spike protein is also preserved even with the newer spike protein mutations, but its activity against the original Wuhan spike protein,(the one vaccines were designed to produce) is fairly well studied at this point.
Abstract:
Background/Aim: Coronavirus disease 2019 (COVID-19) is an infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). One drug that has attracted interest is the antiparasitic compound ivermectin, a macrocyclic lactone derived from the bacterium Streptomyces avermitilis. We carried out a docking study to determine if ivermectin might be able to attach to the SARS-CoV-2 spike receptor-binding domain bound with ACE2. Materials and Methods: We used the program AutoDock Vina Extended to perform the docking study. Results: Ivermectin docked in the region of leucine 91 of the spike and histidine 378 of the ACE2 receptor. The binding energy of ivermectin to the spike-ACE2 complex was -18 kcal/mol and binding constant was 5.8 e-08.
Conclusion: The ivermectin docking we identified may interfere with the attachment of the spike to the human cell membrane. Clinical trials now underway should determine whether ivermectin is an effective treatment for SARS-Cov2 infection.
******************************
The following video [ https://www.youtube.com/watch?v=11Bl2v3BR2M ] explains the multiple mechanisms of the activity of Ivermectin including the ability of the body to maintain its basic defense of the cell nucleus in preserving the body’s ability to produce antiviral proteins, inhibition of RNA dependant RNA polymerase which inhibits the replication of viral RNA (possibly including that from the mRNA vaccine package), the stat 3 human signaling pathway which inhibits the production of blood clots also possibly mitigating some of the vaccines most dangerous side effects. Also discussed is the inhibition of the CD147 pathway by ivermectin which again may block the clumping of platelets due to spike protein either from the virus or possibly the vaccines.
**************************************
IN FACT these Public Health commies do not want you to know about Ivermectin, that’s why they ridicule the drug and its use at every turn and suppress the news of Ivermectin’s effectiveness.
“FRONT LINE COVID-19 CRITICAL CARE ALLIANCE
PREVENTION & TREATMENT PROTOCOLS FOR COVID-19”
****************************
How to get Ivermectin:
https://covid19criticalcare.com/ivermectin-in-covid-19/how-to-get-ivermectin/
OR :
India Mart:
******************************************
I like it when a totally disinterested observor
WITH ABSOLUTELY NO MONETERY INTERESTchimes in on on a topic.