Wednesday, July 14, 2021

Emergent BioSolutions (EBS) updates

The July 6 NYT updated us on shareholder lawsuits against Emergent BioSolutions (EBS), including the lucrative stock trades of Board chair and founder el Hibri ($42 million recently), President Kramer ($10 million) and even board member Louis Sullivan MD, the first black DHHS Secretary, under Bush #1 ($3 million in trades). 

The Biden administration just exercised a contract to buy another $182 Million dollars' worth of smallpox vaccine for the civilian stockpile from EBS. Despite their horrendous track record for manufacturing vaccines.  

But I must remind readers, the USG had a huge old smallpox vaccine stockpile it destroyed (supposedly to save money on electricity) shortly before 2001.  Then the Bush #2 administration bought a shot for every American.  Old vaccine has been shown to retain activity for many years.  

One wonders how much "lobbying" this smallpox vaccine contract cost EBS.  Because it seems this vaccine purchase, by a Democratic administration, will probably stop Democratic Government Reform House members from pursuing their vendetta against the company. Their arrows were focused on crony contracts (especially with Trump's Assistant Secretary for Prevention and Response). Investigating Members promised another hearing on EBS, awaiting the documents EBS had so far failed to provide. But now that Biden's Assistant Secretary for Prevention and Response has ALSO bought smallpox vaccine from EBS, perhaps there won't be another hearing.

EBS is an equal opportunity buyer.  They buy both sides of the aisle. 

But there is even more cringe-worthy material.  Vaccine is being shipped, even though it is adulterated.  That is what can be done under an EUA:  waive the requirement for manufacturing approval.  Read it and weep:  "No corners were cut."  Ho Ho Ho.

The agency has since allowed about 40 million Johnson & Johnson doses manufactured at the factory to be distributed for use — but with a warning that regulators couldn’t guarantee that Emergent had followed good manufacturing practices. Even with the latest batch cleared for release on Friday, Johnson & Johnson remains nearly 40 million doses short of the 100 million doses called for in its federal contract.

Here are some of my recent posts on this company, including discussion of 2 Congressional hearings that talked about EBS.

Some of the voluminous evidence that prior infection confers good immunity while (Israel's Pfizer) vaccination does not

Readers are demanding citations proving natural immunity is far better than vaccine-induced immunity for Covid.  As my readers know I scan large amouns of material and cannot recall all the epi stats on this subject, but below are 4 references I just found, 2 on waning vaccine immunity, one on the rarity of repeat covid infections in healthcare workers, one on repeat infections in Indians.

The other type of evidence is the persistence of T cell immunity after vaccination.  A convincing report on this came out in the past 2 weeks by the La Jolla team of immunologists that includes Shane Crotty.  

https://www.wsj.com/articles/vaccinated-people-account-for-half-of-new-covid-19-delta-cases-in-israeli-outbreak-11624624326

About half of adults infected in an outbreak of the Delta variant of Covid-19 in Israel were fully inoculated with the Pfizer vaccine, according to a clarification by Prof. Balicer of an earlier statement. An earlier version of this article incorrectly said about half of people infected in the outbreak were fully inoculated.

https://www.medscape.com/viewarticle/954357

"As seen in real world data released from the Israel Ministry of Health, vaccine efficacy in preventing both infection and symptomatic disease has declined six months post-vaccination, although efficacy in preventing serious illnesses remains high," the statement said, according to multiple news outlets.

Israeli officials are reporting a 30% decrease in the effectiveness of the Pfizer COVID-19 vaccine to prevent infection and mild to moderate cases. At the same time, however, protection against hospitalization and severe illness remains robust.

The country's Ministry of Health data shows high levels of circulating Delta variant and a relaxation of public health measures in early June led to a drop in the vaccine's prevention of "breakthrough" cases from 94% to 64% in recent weeks.

https://www.nature.com/articles/d41586-021-00071-6

The data suggest that repeat infections are rare — they occurred in fewer than 1% of about 6,600 participants who had already been ill with COVID-19. 

https://science.thewire.in/the-sciences/covid-19-reinfection-rare-natural-immunity-lasts-months-pune-study/

New Delhi: Reinfection among people who have recovered from COVID-19 is rare and natural immunity after illness lasts around nine months, a study involving long term follows up of more than 1,000 people in Pune has found.

According to the Times of India, a study conducted by epidemiologists and community medicine experts from the DY Patil Medical College and Hospital in the city tracked 1,081 people who showed SARS-CoV-2 antibodies during a serosurvey in September last year until this past June. During the nine months of observation, just 13 participants – just 1.2% – were reinfected. The study, which is still in pre-print, also found that all those who were reinfected only had mild cases of COVID-19 and made a full recovery.

2017 article in a Nature journal discusses ivermectin effects (even against cancer) and mechanisms of action.

 https://www.nature.com/articles/ja201711.pdf

Someone wrote this in 2017.  Some people thus knew ivermectin had antiviral properties.  In fact, the drug has all kinds of possibly miraculous effects.  It is just missing the important one:  patentability.  (It was patented but the patent expired in 1997.) 

Recent research has confounded the belief, held for most of the past 40 years, that ivermectin was devoid of any antiviral characteristics. Ivermectin has been found to potently inhibit replication of the yellow fever virus, with EC50 values in the sub-nanomolar range. It also inhibits replication in several other flaviviruses, including dengue, Japanese encephalitis and tick-borne encephalitis, probably by targeting non-structural 3 helicase activity.97 Ivermectin inhibits dengue viruses and interrupts virus replication, bestowing protection against infection with all distinct virus serotypes, and has unexplored potential as a dengue antiviral.98 Ivermectin has also been demonstrated to be a potent broadspectrum specific inhibitor of importin α/β-mediated nuclear transport and demonstrates antiviral activity against several RNA viruses by blocking the nuclear trafficking of viral proteins. It has been shown to have potent antiviral action against HIV-1 and dengue viruses, both of which are dependent on the importin protein superfamily for several key cellular processes. Ivermectin may be of import in disrupting HIV-1 integrase in HIV-1 as well as NS-5 (non-structural protein 5) polymerase in dengue viruses.99,100...

Anti-cancer 

There is a continuously accumulating body of evidence that ivermectin may have substantial value in the treatment of a variety of cancers. The avermectins are known to possess pronounced antitumor activity,107 as well as the ability to potentiate the antitumor action of vincristine on Ehrlich carcinoma, melanoma B16 and P388 lymphoid leukemia, including the vincristine-resistant strain P388.108 Over the past few years, there have been steadily increasing reports that ivermectin may have varying uses as an anti-cancer agent, as it has been shown to exhibit both anti-cancer and anti-cancer stem cell properties. An in silico chemical genomics approach designed to predict whether any existing drugs might be useful in tackling glioblastoma, lung and breast cancer, indicated that ivermectin may be a useful compound in this respect.109 In human ovarian cancer and NF2 tumor cell lines, high-dose ivermectin inactivates protein kinase PAK1 and blocks PAK1- dependent growth. PAK proteins are essential for cytoskeletal reorganization and nuclear signaling, PAK1 being implicated in tumor genesis while inhibiting PAK1 signals induces tumor cell apoptosis (cell death). PAK1 is essential for the growth of more than 70% of all human cancers, including breast, prostate, pancreatic, colon, gastric, lung, cervical and thyroid cancers, as well as hepatoma, glioma, melanoma, multiple myeloma and for neurofibromatosis tumors.110 Globally, breast cancer is the most common cancer among women but treatment options are few. Ivermectin suppresses breast cancer by activating cytostatic autophagy, disrupting cellular signaling in the process, probably by reducing PAK1 expression...

Spain’s top court rules pandemic lockdown ‘unconstitutional’/ The Independent

https://www.independent.co.uk/news/world/europe/spain-rules-pandemic-lockdown-unconstitutional-b1884038.html

Last year’s stay-at-home lockdown order by the government under a state of emergency was unconstitutional, Spain’s constitutional court has ruled on Wednesday.

The court ruling was in response to a suit filed by the far-right Vox party.

It was a split decision according to a brief statement issued by the court. State broadcaster TVE said six magistrates voted in favour and five against.

According to the Spanish broadcaster, the ruling said that the limitations on movement violated citizens’ basic rights and therefore the state of emergency was insufficient to give them constitutional backing.

Spain’s government declared a state of emergency on March 14, 2020, ordering people to stay indoors and leave their homes only for basic shopping for several weeks.

Tennessee's top vaccination official fired (and so, it seems, is the adolescent vaccine program) amidst anger over vaccinating children without parental consent/STAT

https://www.tennessean.com/story/news/health/2021/07/12/tennessee-fires-top-vaccine-official-covid-19-shows-new-spread/7928699002/

On Monday, the state health department also abruptly fired Michelle Fiscus, who served as the state's top vaccination official. Although her termination letter provided no details, Fiscus believed she was fired to appease state lawmakers, who were angered by efforts to vaccinate teens as young as 14 using a legal mechanism that removed the need for parental consent...

https://www.usatoday.com/story/news/health/2021/07/13/tennessee-halts-all-vaccine-outreach-minors-not-just-covid-19/7928701002/

The Tennessee Department of Health will halt all adolescent vaccine outreach – not just for coronavirus, but all diseases – amid pressure from Republican state lawmakers, according to an internal report and agency emails obtained by the Tennessean. If the health department must issue any information about vaccines, staff are instructed to strip the agency logo off the documents.

The health department will also stop all COVID-19 vaccine events on school property, despite holding at least one such event this month. The decisions to end vaccine outreach and school events come directly from Health Commissioner Dr. Lisa Piercey, the internal report states.

Additionally, the health department will take steps to ensure it no longer sends postcards or other notices reminding teenagers to get their second dose of the coronavirus vaccines. Postcards will still be sent to adults, but teens will be excluded from the mailing list so the postcards are not “potentially interpreted as solicitation to minors,” the report states.

These changes to Tennessee’s vaccination strategy, detailed in an COVID-19 report distributed to health department staff on Friday, then reiterated in a mass email on Monday, illustrate how the state government continues to dial back efforts to vaccinate minors against coronavirus. This state's approach to vaccinations will not only lessen efforts to inoculate young people against coronavirus, it could also hamper the capacity to vaccinate adults and protect children from other infectious diseases.

And these changes will take effect just as the coronavirus pandemic shows new signs of spread in Tennessee. After months of declining infections, the average number of new cases per day has more than doubled in the past two weeks – from 177 to 418. The average test positivity rate has jumped from 2.2% to 5.4% in the same time period.

And from the same article:  "If the health department must issue any information about vaccines, staff are instructed to strip the agency logo off the documents."

Tuesday, July 13, 2021

Covid vaccine deaths exceeded Covid disease deaths last week

According to the NYT, there were an average of 255 deaths/day from Covid this past week.  255 x 7 = 1785.

But the federal government added 2,043 deaths to the total count reported to the Vaccine Adverse Event Reporting System (VAERS) last week.  This per Gateway Pundit, but other sites also reported a jump of 2,000 deaths to the reporting system.

Maybe the FDA and CDC, who jointly run the VAERS program, were getting through a backlog of reports.

Nonetheless, more deaths reported after Covid vaccinations than reported after Covid illnesses is food for thought.  The emergency is over.  The risks appear to have overtaken the benefits.  (While I need to acknowledge that the reliability of either number is poor, you still have to admit these are shocking stats.) 

Here is a discussion of the VAERS numbers reported last week in The Defender.

Some states move to block Covid-19 vaccine requirements in public schools/ CNN

https://www.cnn.com/2021/07/13/health/covid-19-vaccine-requirements-schools-analysis-wellness/index.html

A CNN analysis has found that at least seven states -- Alabama, Arkansas, Florida, Indiana, Montana, Oklahoma and Utah -- have enacted legislation this year that would restrict public schools from requiring either coronavirus vaccinations or documentation of vaccination status.

As of June 22, at least 34 states had introduced bills that would limit requiring someone to demonstrate their vaccination status or immunity against Covid-19, according to the National Conference of State Legislatures, which has been tracking legislation related to coronavirus vaccines. At least 13 states -- Alabama, Arkansas, Florida, Indiana, Iowa, Kansas, Missouri, Montana, North Dakota, Oklahoma, Tennessee, Texas and Utah -- have passed them into law, according to the document, and at least six of those include language pertaining specifically to schools or education...

Health Freedom Defense Fund Sues Biden Administration Over Mask Mandate/ press release

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Today the Health Freedom Defense Fund (HFDF) and two Florida residents filed a lawsuit asking the United States District Court in Tampa, Florida to strike down the CDC’s nationwide mask mandate for travel.

“The CDC is not a nationwide police force, and is not empowered to make laws,” said Leslie Manookian, Founder and President of Health Freedom Defense Fund. “Nevertheless, with no legal authority to do so, these unelected, unaccountable technocrats have forced every citizen in America to wear a mask when they travel. We believe that Americans have the right to think for themselves and make their own health care choices without the meddling of government. Americans must not be dictated to in this manner by anyone, let alone unelected, unaccountable technocrats at CDC.”

The nationwide mask mandate was issued by the CDC early in the Biden Administration. Since that time, a Florida Federal Court has struck down the CDC’s cruise line order as unsupported by law, and five justices of the Supreme Court recently appear to have agreed that the CDC over reached with its nationwide eviction moratorium.

“The fact is that the police power — that is the power to regulate the health, safety and welfare of Americans — was specifically reserved to the States by our Constitution,” said George Wentz of the Davillier Law Group, legal counsel for the Plaintiffs. “With the mask mandate, not only does the CDC usurp the role of the States by attempting to exercise general police powers, but at the same time it steps into the shoes of Congress and makes a nationwide law. We are confident that the CDC is way out of bounds here, and the Court will strike down the mask mandate.”

Masks have been approved for use by the general public under an emergency use authorization (EUA) and are considered investigational products under the law. Their efficacy has not been proven, and their short and long-term side effects have not been studied. Recent studies have shown that masks do more harm than good, and expose the wearer to levels of carbon dioxide well above levels permitted by OSHA in the workplace.

Members of Health Freedom Defense Fund feel strongly that they should not, and cannot, be forced to wear masks and that no one should have the power to force another person to cover their airway.

For more information contact us at info@healthfreedomdefense.org

PDF of Complaint

LINK to press release

COVID-19: Should Cases of Guillain-Barré Make a Difference?/ AAPS

 https://aapsonline.org/covid-19-should-cases-of-guillain-barre-make-a-difference/

If you haven’t yet gotten the jab, should the recent reports of Guillain Barré affect your decision?

The FDA is adding a new warning for the Johnson & Johnson COVID jab because of 100 preliminary reports of Guillain-Barré syndrome (GBS) after the administration of 12.8 million doses. Of these reports, 95 were serious and required hospitalization, the FDA statement said, and there was one death.

Most people fully recover from GBS, but some never fully regain their strength or fine motor skills. It may begin with mild weakness and progress to paralysis of the respiratory muscles, so that artificial ventilation is required. Patients may spend a month or more in the ICU and months in rehabilitation. They may face huge medical bills—the jab is “free,” but care of complications is not.

“Only” one case in 128,000 may be called “rare,” and it might not have been caused by the jab. Each year in the United States, an estimated 3,000 to 6,000 people develop the illness. But in 1976, swine flu vaccines were stopped for one case of GBS in 100,000 doses.

“Available data do not show a pattern suggesting a similar increased risk of Guillain-Barré with the Pfizer-BioNTech and Moderna vaccines,” states the Washington Post. “More than 321 million doses of those vaccines have been administered in the United States.”

However, as of today, the Vaccine Adverse Event Reporting System (VAERS) contains reports of 9,048 deaths, 7,463 persons disabled, and 26,818 hospitalizations.

The more user-friendly British Yellow Card System contains reports of 40 cases of GBS with two deaths, and 43,738 “nervous system disorders” with 43 deaths for the Pfizer productFor Moderna, there was only one nonfatal case of GBS listed and 3,331 “nervous system disorders” with two deaths.

“Federal health officials have repeatedly emphasized that the benefits of the coronavirus inoculations far outweigh potential risks,” says the Washington Post. But on the individual level, the calculation is not simply population-wide reported COVID deaths vs. reported vaccine deaths. Issues are:

  • What is the risk of getting COVID in my circumstances and location?
  • What is the risk of complications for a person of my age and health status?
  • What is the risk of breakthrough cases? We need to know the cycle threshold (Ct) to judge whether diagnosis accuracy is comparable for persons with or without the jab.
  • What is the true level of complications? Might there have been 90,000 deaths if only 10% are reported to VAERS?
  • How do we distinguish deaths FROM vs. WITH COVID or vaccine? Is it the same way for both?

Some would like to punish those who decide that for them, the risk of the jab exceeds the benefit. Dr. Leana Wen of CNN, former head of Planned Parenthood, wants to make the choice of being unvaccinated hard and unduly burdensome. This is presumably to protect the public from catching the virus from an unvaccinated person. However, Moderna and Pfizer vaccine trials “have explicitly acknowledged that their gene therapy technology has no impact on viral infection or transmission whatsoever and merely conveys to the recipient the capacity to produce an S1 spike protein.”

For further information on physicians’ opinions and first-hand reports on adverse reactions by patients, family members, and physicians, see links in AAPS survey results: Majority of Physicians Decline COVID Shots, according to Survey.--by Jane Orient, MD

Monday, July 12, 2021

Boosters: Creating the appearance of scarcity by having Tedros beg the rich countries not to start boosters while the poor countries still lack first jabs

https://www.nytimes.com/live/2021/07/12/world/covid-coronavirus-updates#pfizer-booster-vaccine-fda-cdc

The NYT even has an online video of "seriously disappointed" Tedros.

But there's more!  This weekend was all about England vs. Italy.  But today, it's all about Pfizer vs. Regulators.  Their battle was carried out online, and the NY Times provides the post-game analysis.

Israel even got into the act, starting third doses on the immunocompromised today...no doubt timed by Albert Bourla as another act for today's 3 ring circus performance.  The Pfizer meeting involved, according to the Times, "virtually every top doctor in the federal government."  

The take-home message, just in case you missed it, is that the careful, scientific US government regulators really care about this decision, and they will protect you from big bad Pharma.  They won't start those boosters till you REALLY need them.

Ignore those CDC briefers behind the curtain, who asked their advisory committee members on June 23 to approve boosters without any data showing they were needed. 

Representatives of Pfizer met privately with senior U.S. scientists and regulators on Monday to press their case for swift authorization of coronavirus booster vaccines, amid growing public confusion about whether they will be needed and pushback from federal health officials who say the extra doses are not necessary now.

The high-level online meeting, which lasted an hour and involved Pfizer’s chief scientific officer briefing virtually every top doctor in the federal government, came on the same day Israel started administering third doses of the Pfizer-BioNTech vaccine to heart transplant patients and others with compromised immune systems. Officials said after the meeting that more data — and possibly several more months — would be needed before regulators could determine whether booster shots were necessary...

Because no animal reservoir has been found for SARS-CoV-2, it cannot properly be termed a zoonosis.* Should we call it a labnosis? And what does that mean?

After a year and a half of seeking but not finding SARS-2 in any wildlife anywhere (apart from domesticated or zoo animals that appear to have caught it from humans) is it time to say, yes, it didn't just escape from a lab?  It was created, built, assembled in a lab. Or more probably, many labs.

Coronavirus scientists have been constructing new viruses out of bits and pieces of other viruses for a long time.

Why did they do it?

One answer is that it was relatively easy to do.  Easier than for many other viruses.  Scientists like to tinker.

Okay, but after the SARS-1 outbreak in 2002-3, and a series of SARS-1 lab leaks over the ensuing several years in China, Taiwan and Singapore, which killed a few people, especially lab workers, didn't scientists know it was dangerous to do this?

SARS viruses were designated by the US government as "Select Agents," meaning they had the potential to cause a deadly pandemic and/or severe economic damage to crops or livestock.  Scientists had to handle them in special ways, and get permission to transfer or share them with other labs.  Scientists working on SARS coronaviruses had to have been aware of the risks in what they were working on. 

I previously cited a statistic from STAT.  The statistic is that Fauci's NIAID has been funding coronavirus research for over twenty years, and at a price of up to $51 million per year, pre-Covid.  Until 2002, everyone thought that the worst thing coronaviruses did to humans was cause colds:  10-30% of all colds.  NIAID doesn't spend money on colds.

Coronaviruses do cause animal diseases.  But still, animal diseases are not in NIAID's bailiwick.  USDA funds research on them.

Some coronavirus research made sense, such as the 2005 CDC study that showed chloroquine killed SARS-1 at achievable human doses, in the test tube.  Or the 2014 NIAID study that showed chloroquine killed MERS.

But no new drugs or vaccines came out of the hundreds of millions of dollars in coronavirus research sponsored by NIAID.  And when Covid hit, Fauci and his NIAID hid information on the drugs they had found to be effective against coronaviruses in the lab.

So, what were Fauci and NIAID actually doing with all the coronavirus research?  What were they looking for?

It seems they were remarkably successful in creating new chimeric, pathogenic coronaviruses.  But they buried the research on effective treatments.

Americans need to ask, what in heaven's name were Fauci and his masters trying to accomplish?  Who are his masters?  And what other deadly viruses have they created, with or without their friends in Wuhan?

We need to know what they heck they were doing.  What did these programs create?  Why did these programs exist?  Is anyone in media asking these questions?

We need to know now, before the fear of the variants wears off, and people refuse the lockdowns and any more vaccines.  Who knows--that could be the trigger for the next dangerous bug to be unleashed.

* https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725765/pdf/fpubh-08-596944.pdf

Other than circumstantial evidence of zoonotic cases in mink farms in the Netherlands, no cases of natural transmission from wild or domesticated animals have been confirmed. More than 40 million human COVID-19 infections reported appear to be exclusively through human-human transmission. SARS-CoV-2 virus and COVID-19 do not meet the WHO definition of zoonoses. We suggest SARS-CoV-2 should be re-classified as an EID of probable animal origin.

Sunday, July 11, 2021

Doctor in Lytton, British Columbia goes public over severe Covid vaccine injuries in April. In June the doctor's entire town burns to the ground.

It's probably a coincidence.  Like all those California fires.  It got extremely hot, like the Sahara Desert, in British Columbia. And then there was a wildfire.

There seems to be nothing left of Lytton, B.C., where Dr. Charles Hoffe worked as a family practitioner for the past 28 years.  He began speaking out when his patients suffered severe consequences after their Covid vaccinations.

Dr. Hoffe's story.

Lytton, B.C. after the fire.

Lytton evacuees get first look at devastation in fire-ravaged village
 

Last Updated Jul 9, 2021 at 11:02 pm PDT

‘Lytton is gone’: Accounts of death, destruction in Canadian village that caught fire in record heat

Saturday, July 10, 2021

Sneak attack: Congress likely to give Covid vaccine mfrs a liability waiver that will cover them after the EUAs are gone

Let me just say one thing.  If Congress wanted to make vaccines safe, there is a very easy way to do so.  Simply lift the liability waiver and the manufacturers will stop selling those vaccines that are unsafe.

From the press release:

https://doggett.house.gov/media-center/press-releases/bipartisan-members-introduce-legislation-modernize-vaccine-program

The Vaccine Injury Compensation Modernization Act, legislation introduced by Rep. Doggett and Rep. Upton, is among several vaccine-related measures which will be heard before the House Energy & Commerce Health Subcommittee at 10:30 am, next Tuesday, June 15.

“This legislation updates an important consumer protection tool to assure it is capable of fairly addressing the one-in-a-million injuries that may be associated with COVID-19 vaccines,” said Congressman Doggett. “Though misinformation spreads and anti-vaxxers continue to fearmonger, vaccine-related injuries are extremely rare, usually caused by an error in administration rather than the vaccine itself. Providing complete information and assuring a prompt and fair response to any lasting injury represents an effective way of addressing vaccine hesitancy.”

“The number of new vaccines we’ve seen over the past year highlights the urgent need for us to update the Vaccine Injury Compensation Program as we work to ensure vaccines remain safe and effective tools to combat public health challenges,” Congressman Upton said. “The government, vaccine producers, and the general public all share an interest in ensuring the vaccines we bring to market are always safe. The bipartisan Vaccine Injury Compensation Modernization Act would help us do just that.”

“Right now, it takes an act of Congress to add vaccines to the Vaccine Injury Compensation Program. This bipartisan legislation will allow the Department of Health and Human Services to add to the list of eligible vaccines covered by the program, including the new COVID-19 shot. This will give Americans more peace of mind and help put this pandemic behind us even faster!”said Congressman Kelly.

The Vaccine Injury Compensation Modernization Act, introduced by Rep. Doggett and Rep. Upton, would:

  • Reduce case backlog by expanding the number of Special Masters (judges for the VICP) from a ceiling of 8 to a floor of 10.

  • Increase transparency by requiring the Special Masters to provide an annual report on caseload, number of pending cases and whether hearings have been scheduled, how many days it took for cases to receive a judgment, how many cases received a judgment and the results, and any recommendations regarding the need for more Special Masters.

  • Provide fair compensation by increasing the cap on damages to the amount it would be today based on inflation increases and establish an inflation-based formula to automatically increase the cap moving forward.

  • Ensure consumers have sufficient time to file claims by increasing the statute of limitations from 3 years to 5 years.

  • Expedite the addition of new vaccines to the program [the "program" is the VICP, which gives manufacturers of all vaccines recommended on the childhood schedule and during pregnancy an automatic liability waiver--Nass] by requiring HHS to promulgate rulemaking to add a CDC-recommended vaccine or injury to the injury table within 6 months of a recommendation rather than 2 years.

  • Expand the types of vaccines eligible for coverage under the VICP by including vaccines and injuries recommended by the CDC for routine administration in adults. [Coverage means a manufacturer liability waiver, and the timing relates to getting the Covid vaccines liability waivers once they are licensed, because the waivers would otherwise end with licensure.--Nass]

    The Vaccine Access Improvement Act, introduced by Rep. Doggett and Rep. Kelly, would:

    Streamline the application of the 75-cent excise tax on covered-vaccine doses by eliminating the requirement that Congress pass legislation to apply the tax each time a new vaccine is added to the VICP. The tax would now be automatically applied once HHS adds a vaccine to the injury table.

    “This legislation provides critical updates to the National Vaccine Injury Compensation Program ensuring the public has a vibrant safety net for all those who protect their families and communities by getting vaccinated. The increase in

the number of Special Masters will dramatically reduce the overburdened dockets and the increased compensation brings the 32-year-old Program up-to-date, as Congress promised,” said Prof. Renée Gentry, Director of the Vaccine Injury Litigation Clinic, George Washington University Law School.

The Vaccine Injury Compensation Modernization Act and the Vaccine Access Improvement Act are endorsed by BIO, American Pharmacists Association, and National Community Pharmacists Association.

In February, Congressman Doggett chaired the first Health Subcommittee hearing of the 117th Congress, “The Path Forward on COVID-19 Immunizations.” During this hearing, Dr. Ashish Jha, Dean of the Brown University School of Public Health, testified in support of modernizing the VICP and noted its importance in promoting vaccine confidence. You can view Dr. Jha’s oral testimony here and read his written testimony here.

Fauci, king of mixed messages, pretends the federal government knew nothing about Pfizer applying to authorize boosters/RT

Ever get the feeling that Fauci, Walensky and the rest are playing with you?

"White House Covid-19 adviser Anthony Fauci said Pfizer gave the feds no warning before announcing that it would seek emergency approval for a third vaccine dose, maintaining that, for now, booster shots are unnecessary."

If that was true, why did the CDC ask its advisory committee to consider giving boosters early in the fall on June 23?  If booster doses have not received an emergency use authorization by the fall, how could they be given in the fall?

However, the health adviser [Fauci] also noted that studies into additional doses are ongoing within the Food and Drug Administration (FDA), the Centers for Disease Control and Prevention (CDC), as well as the National Institutes of Health, suggesting they have not been ruled out for good...

Fauci, however, said the announcement took him by surprise. He told Blitzer that Pfizer CEO Albert Bourla even contacted him to apologize for not giving a heads up. While the CNN host suggested US health officials might not be “on the same page” with pharma firms when it comes to booster shots, Fauci insisted that is not the case. 

“Wolf, we are on the same page,” he said, later adding, “It appears to be a mixed message, but it’s not. The message is very clear: The CDC and FDA say if you’ve been fully vaccinated, at this point in time you do not need a booster shot.”

UPDATE July 11:  And on Twitter the trolls are out demanding the boosters and fearmongering.  For example:

https://twitter.com/32bitmodeling/status/1414249253153644546

"They are responding to the ridiculous obstinance of US gov't. It is 100% clear we will need booster development.

Why? Because if we don't act like we need them now, we won't have them in fall when we might need them immediately." 

Newest method to confuse the public: are boosters needed or not? No, but they will be here soon regardless, garbed in The Science, of course

To all appearances, the CNN story below concerns a duel between Pharma Giant Pfizer, which wants to sell new vaccine for variants, and 3 federal agencies, who say we don't think they are needed yet and we will determine with the SCIENCE when they will be needed.  Sounds good.  For once the feds are speaking up. Science over profit.

But is that really what is going on?

A mere two weeks earlier, at the CDC's vaccine advisory committee meeting, the advisors were asked to give CDC the go-ahead to begin giving boosters in September, without the evidence to support such boosters.  Remember, every word out of a CDC briefer's mouth has been checked and rechecked before the meeting.  Here is my live blog of that meeting, and here is what CDC doctor Sara Oliver said about this issue on June 23:

CDC is doing studies to look at antibodies at 6 months...suggesting its plan is to administer boosters every six months. By early fall CDC will have lots of data to justify boosters. ACIP will be meeting to vote on boosters then. The CDC working group said it would consider boosters if there is evidence of vaccine protection waning or if variants occur which escape vaccine protection. Sara's voice gets a little sad here. How can it be that the working group wants evidence that boosters are needed before recommending them? Can't ACIP recommend boosters already, based on the risk of disease? (I.e., based on the supposition they might be needed?). Then Amanda Cohn, another CDC staffer with a little more experience, piped up.

"The more data we wait for, the more preventable cases may occur," she asserted solemnly.  In other words, ACIP members, give us at CDC the wink to let us know we can convene you again soon to approve the boosters.  In other words, can't we just fuggedabout the data? Various members made fatuous comments, and then Amanda returned. She is SO relieved. Her ACIP members are even more supine than she expected. Now she is asking them to commit to when she can start the boosters!

Jose Romero, the chair, says they have given CDC "the information they were looking for." Yup. ACIP kissed the ring again.  This is truly a travesty.  I've got a new name for ACIP: Boosters 'R Us
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Now, below, you can read about the charade being orchestrated now, so that you never realize that the plan to start boosters is already in place.  The ACIP approval meeting is coming up.  Booster shots will start in September or October. And everyone can claim the goverment held fast against a precipitous push by Pfizer for early boosters.
And everyone wins but the public, for whom boosters appear to be totally unnecessary.

https://www.cnn.com/2021/07/08/health/pfizer-waning-immunity-bn/index.html

...Hours after Pfizer issued its statement promoting boosters on July 8, the FDA and Centers for Disease and Control issued a joint statement saying Americans do not need booster shots yet.

    "Americans who have been fully vaccinated do not need a booster shot at this time," they said.
      In a statement to CNN on Friday, the World Health Organization said, "We don't know whether booster vaccines will be needed to maintain protection against COVID-19 until additional data is collected," adding, "limited data available on how long the protection from current doses lasts and whether an additional booster dose would be beneficial and for whom."
      Pfizer and its partner BioNTech said evidence was building that people's immunity starts to wane after they have been vaccinated. The Pfizer vaccine requires two doses to provide full immunity.
        "As seen in real world data released from the Israel Ministry of Health, vaccine efficacy in preventing both infection and symptomatic disease has declined six months post-vaccination, although efficacy in preventing serious illnesses remains high," Pfizer said in a statement emailed to CNN.
        "Additionally, during this period the Delta variant is becoming the dominant variant in Israel as well as many other countries. These findings are consistent with an ongoing analysis from the Companies' Phase 3 study," it added.
        "While protection against severe disease remained high across the full six months, a decline in efficacy against symptomatic disease over time and the continued emergence of variants are expected. Based on the totality of the data they have to date, Pfizer and BioNTech believe that a third dose may be beneficial within 6 to 12 months following the second dose to maintain highest levels of protection." It gave no further details.
        The announcement could have implications across the world. The Pfizer shot is the cornerstone of vaccination programs in many countries. Two-thirds of doses delivered across the European Union were made by Pfizer, according to the European Center. In Israel, Pfizer is the only vaccine used.
        Of the 158 million fully vaccinated people in the US, more than half received the Pfizer shot.
        US government officials have stressed that fully vaccinated people have a low risk of infection, even from the Delta or B.1.617.2 variant, which is more transmissible than earlier lineages of the virus.
        Plus, several studies have indicated the mRNA vaccines made by Pfizer and Moderna confer longterm protection.
        "FDA, CDC, and NIH (the National Institutes of Health) are engaged in a science-based, rigorous process to consider whether or when a booster might be necessary. This process takes into account laboratory data, clinical trial data, and cohort data -- which can include data from specific pharmaceutical companies, but does not rely on those data exclusively," they added.
        It was a clear message to Pfizer, which has been hinting at the need for a booster shot for months.
        "We continue to review any new data as it becomes available and will keep the public informed. We are prepared for booster doses if and when the science demonstrates that they are needed," the CDC and FDA said in the statement...