Back in Haiti during 2010, UN Peacekeepers from Nepal, who were infected with cholera, build their encampment on a river which supplied a large number of Haitians with their water. The result was a multi-year epidemic, killing at least 10,000 Haitians. The CDC (under Obama and Hillary's State Dept.), tried to shift blame away from the real cause. When that failed and the true origins of the epidemic became known, CDC said they didn't come forth with the information sooner, due to "political considerations."
Horrible story!
https://observer.com/2017/03/emails-reveal-cover-up-hillary-clinton-cholera-haiti/
Around 2011, the Cochrane Group, which does/did top notch meta-analyses of published medical studies, found that approximately 75% of people with hypertension did not need to follow a low-sodium diet. In fact, there was a sub-group of individuals who actually had more cardio-vascular issues when they followed sodium restriction guidelines.
The CDC was heavily invested in pushing a sodium restricted diet of 2300mg. per day for just about everyone and then quietly commissioned their own study. The findings of Cochrane were robust, but CDC never came out and reversed their message. They just slowly, over several years, stopped advertising the message.
I remember this distinctly, because my father loved his salt, and for the last 5 years of his life, followed a disgusting low sodium diet.
It's the govt. that's doing all the pushing (and advertising). It doesn't look good when huge numbers of vials are thrown away. I just did a quick search and found that there's a number of media sites which routinely report on which states and companies dump unused vials.
I wonder is some of it also could be to get all these people to have the jabs, so the govt. can turn their media blitz to the "boosters" and the school kids.
Some of it could be the expiration dates. Sorry this is from NPR, but apparently Alabama is sitting on a lot of vaxx poison that will expire at the end of August.
They tested for the presence of antibodies against the S-1 portion of the spike protein. 83.3% of the pop. was estimated to have these antibodies (via infection or vaccination) by 5/21. Description of the CDC study:
https://www.cdc.gov/coronavirus/2019-ncov/cases-updates/blood-bank-serosurvey.html
Results published in yesterday's JAMA:
That is interesting! I was wondering the other day whether a combination of zinc, quercitin and Ivermectin were required for a prophylactic cocktail, if they both worked via the same mechanism. I wasn't sure Zelenko was correct, but now perhaps, all are needed since they attack the virus in different ways.
I just finished watching the video of the latest meeting of the NYSDOH Health Planning Council meeting, the body that deals with codes & regulations. There are big problems on the horizon (mentioned by someone from W. NY) with long term care facilities. A survey of unvaxxed LTC workers indicated that half will refuse the jabs. There's also a problem with a large number of Home Health Aides, who will be refusing. Things may get interesting in the future, with the Chair suggesting a possible modification of the vaxx mandate in certain health sectors and/or regions.
If you're interested in watching the chicken game unfold, the archives of the Planning Council meetings are located at:
Trump gave a warning about this earlier this year, when he talked about how the vaccines produced during his Presidency were "safe." I suspect that the clot shots are becoming increasingly more toxic over time, but the trend may be hidden, since the elderly and infirm were first to get the vaxx.
Ardis argues that some types of flu vaccine are worse than others in side effects, and those selected this year are going to result in a higher-than-average # of Guillain-Barre cases. CDC claims that this "mystery illness" peaks on even-numbered years since 2014, so this year will be another upswing.
Summary of Interview: In August, CDC sent out a blast to hospitals/doctors, warning them of a future upswing in cases of a "polio-like" illness among children (average age=5 yrs.), expected to last through Nov. Symptoms include paralysis of limbs and face and no cure exists . Drs./hospitals are instructed to diagnose symptoms as "Acute Flacid Myelitis."
Dr. Ardis argues that it's really Guillain-Barre Syndrome and is a side effect from the type of flu vaccines administered this season. CDC has known about this type of vaccination side effects in children since 2001, but approves them anyway.
Other interesting info: Pfizer, Moderna and J&J can change ingredients in their vaxxs anytime while under EUA, without notifying govt. or the public. Moderna started out with 2 "patentable" ingredients in Dec. 2020 and now has 7!
Teaching shortages too! The best and brightest will be leaving, rather than deal with the mandates. NYS will be left with the crazy SJWs and "Wokes."
According to the National Education Association, roughly 30% of members have left the teaching field early due to the pandemic.
https://cbs6albany.com/news/back-to-school/teacher-shortages-impacting-capital-region-schools
Protease inhibitors for HIV theoretically target viral replication, and according to Pfizer, they do the same for SARS-COV2.
BUT, according to the COVID docs, zinc+ quercitin inhibit replication. So why would anyone want an HIV medication that fails unless it's used with other protease inhibitors?
Ritonavir is also called NORVIR. Here's the "informed consent" info on the website.
SAFETY CONSIDERATIONS
Do not take NORVIR with certain medicines, as these can cause serious or life-threatening problems such as irregular heartbeat, breathing difficulties, or excessive sleepiness. Do not take NORVIR if you have had a serious allergic reaction to any of its ingredients. Some patients taking NORVIR may develop liver and pancreas problems, which can cause death. Patients may develop large increases in triglycerides and cholesterol, diabetes, high blood sugar, changes in body fat, increased bleeding in people with hemophilia, allergic reactions, and/or changes in heart rhythm. You may develop signs and symptoms of infections that you already have after starting anti-HIV medicines. Please see the Important Safety Information for more details.
I was just listening to an interview w/Reiner Fuellmich from 2 days ago, where he provided an update on activities in his network. He said that, within the next 2 weeks, a class-action lawsuit will be filed on behalf of municipal employees (fire, police) in San Francisco, LA and Sacramento. Approximately one-third to one-half are refusing to be vaxxed.
Below are links to the 2-part intrview:
I was looking over the local obits today and noticed a co-worker's family member (age 52) died from a "sudden illness." The obit said he was an RN from a large health facility that recently mandated vaxxs. I think we'll be seeing more and more "sudden illnesses" to come.
There's a lot of wiggle room for formulation under an EUA, which we've suspected all along with the saline shots, possible variation in dosage strength and "hot lots." Once a drug is FDA-approved, it needs to conform to the stated ingredients, strength and purity. What's going into people's arms right now is still anyone's guess.
Question for OP---Docs are licensed by the state boards, not their employers. Would discipline by Aurora influence the licensing board to bring action against them?
Kudos to anyone who leaves this craziness! I look forward to the day when we have independent medical practitioners back!
I think you're correct about the "house cleaning." It looks like Gruber may have been taken off the "sprint" to get Pfizer approved back in July:
The process requires FDA staff to review millions of pages of complex data, conduct plant inspections, and negotiate with Pfizer over issues including the terms of the FDA’s approved label and the company’s postmarketing responsibilities. Now, the senior agency official said, the agency will initiate a “sprint.”
Under the FDA’s new plan, the director of FDA’s biologics center, Peter Marks, will largely oversee review of the Pfizer application, taking over for Marion Gruber, a 32-year veteran of the FDA who currently heads the office of vaccine research and review within the larger biologics center, according to a second FDA source. A third source familiar with the plan, who like the others spoke on condition of anonymity, said Marks was heavily involved in the review, but did not comment on whether he was formally replacing Gruber in the agency’s chain of command.
Coincidence, but I just ran across this interview with Dr. Jason Alexander, who describes how CDC messed up testing in the early part of the scamdemic.
https://www.brighteon.com/88a3f453-2c64-4d32-95fb-4b68b0534376