Archive for January, 2023

More Bots Pushing COVID Shots

http://  (Approx. 11 Min)

FAKE Doctors Caught Pushing COVID “Vaccine” in Psy-Op Campaign

Redacted With Clayton Morris

Jan. 9, 2023

Dr. Fauci is trying to get out front of the Twitter files that have to do with him and his role in the pandemic. Or so it seems because he is doing the media rounds about the Covid vaccine and adverse events. Isn’t he supposed to be retired? His allies are quickly disappearing on Twitter because they were fake accounts.

This is not the first time Bots pushed a narrative.  Back in Aug. 2021, bots within social media algorithms were used to not only identify and eliminate certain facts and truths, but these AI systems are also being used to promote certain types of propaganda, to brainwash the public into accepting falsehoods as if they are popular messages of truth. To make matters worse, unscrupulous operatives are using vaccine propaganda BOT FARMS to catapult Big Pharma’s lies across social media, to instill fear in the public and advocate for more government and corporate control over lives. The latest bot farm was caught spreading lies about the unvaccinated to garner public support for vaccine passports and a system of segregation against healthy, naturally-immune people.  The BOTS did the following:

  • Personalized messages are being sent en masse & verbatim across several media platforms using fake bots
  • These are fake accounts not sent by real healthcare professionals
  • There may be paid internet trolls involved
  • Bot farms can be controlled from a single computer, hooked up to multiple phones & social media accounts
  • This deceptive propaganda is being used to gain acceptance for lockdowns, shame and segregate the unvaccinated, discourage and demoralize people from speaking out and taking action and to give the impression that a lie is a universal truth accepted by many
  • Do not engage these bots as they are programmed to defend an agenda
  • One such fake message as seen from top graphic states:

“I just left the ER. We are officially back to getting rushed by COVID-19. Delta Variant is running rampant and it’s MUCH more transmissible than the original virus. 99% of our ICU admits did NOT receive a vaccine.”

Our government is also involved by censoring and disinforming the public due to conflicts with Big Pharma.

Category:

Uncategorized

Post-Treatment Lyme Disease Syndrome & Language Fluency Deficits

https://academic.oup.com/acn/advance-article-abstract/doi/10.1093/arclin/acac095/6955887?

Language Fluency Deficits in Post-treatment Lyme Disease Syndrome

Marianne Gorlyn, John G Keilp, Brian A Fallon
Archives of Clinical Neuropsychology, acac095, https://doi.org/10.1093/arclin/acac095
Published:  22 December 2022

 

Abstract
Objective

Recent neurocognitive studies of patients with post-treatment Lyme disease syndrome (PTLDS) find consistent deficits in memory and processing speed. Language fluency deficits are observed as well but may be secondary to poor memory and slowing rather than an independent deficit.

Method

This study performed a secondary analysis of data presented previously, including individuals with PTLDS and comparison samples of healthy volunteers (HC) and patients with major depressive disorder (MDD), to determine if language fluency deficits could be accounted for by poor performance in these other neurocognitive domains.

Results

Basic verbal abilities, memory, and processing speed were all significantly associated with fluency performance. MDD patients’ fluency deficits relative to HC were accounted for by these covariates. However, PTLDS patients’ poorer fluency performance relative to both other groups was not.

Conclusions

Language fluency appears to be an independent area of neurocognitive deficit within the constellation of PTLDS symptoms.

_________________

**Comment**

Again, the PTLDS moniker needs to be eliminated.  It is built on an entirely faulty premise.

For more:

Category:

Lyme, Psychological Aspects, research

COVID Gene Therapy Injections Developed by U.S. Military Are Called “Counter Measures” & Were Ordered As “Prototypes”

**UPDATE Aug., 2023**

“Fact-checkers” continue to deny that the clot shots are gene therapy which contradicts the FDA’s own definition as well as Moderna’s Securities and Exchange Commission filings.  Further, the shots fulfill none of the original definitions for a vaccine.  The definition of vaccine was changed to include the experimental COVID gene therapies and a FOIA shows that the reason for the change was simply to shut down arguments by “right-wing COVID-19 pandemic deniers” that “COVID-19 vaccines are not vaccines per CDC’s own definition.”

While the report below is imperative to understand, so is the information in this article which exposes the military think tank side of all of this. This one minute video by former Pharma research and development executive Sasha Latypova exposes how General Talley of the DOD and others repeat the phrase ‘whole of government’ ad nauseum in press conferences which refers to preemption of state authority and state court jurisdiction due to federal jurisdictional issues. HHS secretary Azar started incorporating it into PREP Act declarations, and seems to originate from the 2010 National Security Strategy document by Obama, cited in 2012-2016 MCMI strategic plan.

This plan particularly targets the “vaccinated” in a globe-spanning military operation by destroying human autonomy by centralizing power and using implanted technology (making humans bioreactors) to reduce the population, provide mass surveillance, and tyrannical control of people’s movements.  While Charles Lieber, who created the nanotechnology, was found guilty of lying about Chinese funding, his work continues through Jia Lui of Harvard who patented Lieber’s work  (nanoscale wires/electronics which can be embedded in biological structures such as tissues and organs to apply an electrical stimulus to the biological structure).  

http://  (Approx. 1 Hour 50 Min.  Scroll to 39:00 to hear Latypova)

Report Shows DOD Controlled COVID Program from the Beginning

Jan. 5, 2022

Redacted

BOMBSHELL new report shows that the Department of Defense controlled the COVID-19 Program from the very beginning… and everything we were told was political theater to cover it up. These documents were obtained by a former executive of a pharmaceutical Contract Research Organization Sasha Latypova.  Excerpt:

Pfizer-BioNTech is really a 3-party R&D alliance: Fosun-Pfizer-BioNTech, and by “party” I mean that one of the three is the Chinese Communist Party. Fosun is a huge Chinese conglomerate that owns a large number of global companies, and its chairman Guo Guangchang is a very high ranking member of the CCP. It is curious that the US DoD awarded $10 billion (Pfizer’s Operation Warp Speed/DoD/BARDA contract) to a venture whose substantial equity (and IP) holder is the the Chinese Communist Party. 

Latypova explains that within the documents, the injections are called “Counter Measures,” which the DOD ordered as “prototypes,” from private manufacturers.

For anyone paying attention, Dr. David Martin explained early on that these are not “vaccines,” but rather gene therapy injections – which allows manufacturers to by-pass normal safety testing commonly used with vaccines. Go here for an important article on how and why the Associated Press is lying about this fact.

Latypova also has written this article on the variability of the shots as well as the fact they are highly unstable, degrade rapidly, and will not distribute evenly as they are manually made water-fat mixtures with fat tending to float to the top, especially after several hours. Some doses will contain 50%+ more mRNA which would introduce 5-6 trillion extra mRNA molecules in the injection which will distribute all over the body in minutes, rapidly make toxic spikes, and may kill a person quickly.  One ex-pharmaceutical exec calls the injections “garbage soup.”

None of this was tested by any regulator as no acceptance criteria for vials/doses exists.

The video wraps up at about 54:10 where Morris states COVID was planned in 2013 and then questions the future.  From the documents, both Morris and Latypova agree that ‘the powers that be’ are already planning the next pandemic with the next thing on the list being to give up our sovereignty under the WHO under international health regulations so the WHO can declare a ‘pandemic’ anytime they want to, which is exactly what they’ve done numerous times before and most recently with COVID when there were only 40 cases worldwide.  This move would allow the WHO to become a global health dictatorship superseding the US Constitution, rendering individual rights null and void. Many state that despite experts defying the narrative, they could even declare a “climate change” pandemic to lock us down.

Go here for another interview of Latypova with Christine Dolan (host) and Katherine Watt (US paralegal) as they expose how the PREP Act and Countermeasures programs were used to completely bypass Constitutional Law and implement terror on the American public.

For a clear picture of the monopolization within health in action, learn how The Cares Act  holds hospitals hostage by bribing them with bonus incentive payments, medically kidnapping patients making them virtual prisoners.  Many have had to resort to the courts to get their loved one life saving treatment, which is currently banned for use by ‘the powers that be.’

The monopolization of mainstream & social media, Big Tech, asset management firms, research, public health, and mainstream medicine must be stopped or doctors & patients will have no voice and no choice.

Monopolization is the endgame.  For those of you who believe the government is the best entity to rule/decide everything, I ask you to reflect upon the rife conflicts of interest and how it has treated Lyme/MSIDS (and many other issues) for over 40 years. Then there’s the most current example of COVID, which has been handled abysmally, which one doctor states is “completely stupid” and “unethical,” and chronicles here.  A similar chronology states many of the same things.  Even CDC director Walensky freely admits the CDC bungled the affair, but she offers no meaningful change, and even has the audacity to ask for more funding.  Please do not bury your head in the sand.  Wake up and smell the coffee before it’s too late.

https://healthimpactnews.com/2023/the-covid-19-vaccines-are-weapons-developed-by-the-u-s-military/

The COVID-19 “Vaccines” Are Weapons Developed by the U.S. Military

Comments by Brian Shilhavy
Editor, Health Impact News

With more of the American public waking up to the fact that the COVID-19 shots are linked to the epidemic of “sudden deaths,” these rushed-to-market emergency use authorized (EUA) “vaccines” are gaining more scrutiny by many in the Alternative Media, and there is now ample evidence that the U.S. Department of Defense has been behind the funding and development of these shots from the beginning.

First referred to as the “War Against the Virus” by President Donald Trump in 2020, it is obvious now that this was a planned military operation all along, and the military operation that released federal funding to fast-track these weapons of mass destruction that are called “vaccines,” was also given a military name: Operation Warp Speed.

The U.S. Military program is a huge black hole that swallows $TRILLIONS each year, and we don’t even know where half of that money goes, because the Pentagon has failed all of its audits for the past 5 years, and in 2022 it could not account for over half of its assets. (Source.)

They don’t even pretend to be fixing this problem anytime soon, because they have publicly stated that they “hope” to be able to pass their first audit by 2027. (Source.)

After two years of funding military spending on COVID “Counter Measures” to fight the “unseen” enemy of “COVID,” much of that funding switched over to Ukraine at the beginning of 2022.

The Brownstone Institute has just published a nice summary of the evidence that none of the EUA shots would have been possible without the U.S. Military, and that most of this has been hidden from the public.

I appreciate that The Brownstone Institute offers the Creative Commons license to allow others to copy and republish their work, as does Health Impact News.

This allows for the greatest distribution of information that is vital to the public, even though other publishers routinely use our articles and graphics without properly attributing it, as is required by the Creative Commons license.

More and more of the content published by the Alternative Media is moving to Substack.com, where the author can put up a paywall to access it.

As I have previously written, many of the same capital venture companies that fund Substack.com also fund other social media companies, like Twitter. See:  Protecting Your Privacy Should be a High Priority in 2023 – Beware of Substack!

And while I do make contributions to the independent publishers who request donations if I use their material, I will not give my credit card and personal data to Substack.com. In 2020 the platform “accidentally” revealed thousands of emails of their subscribers. (Source.)

I don’t know where Brownstone’s funding comes from, but at least you can read their articles for free without them collecting any personal information about you. The founder, Jeffrey A. Tucker, is also a Senior Economics Columnist for Epoch Times. (Source.)

The Epoch Times does require a paywall for most of their articles, even though they appear to be well-funded by Chinese dissidents from the Falun Gong Christian sect, according to Wikipedia.

Did National Security Imperatives Compromise COVID-19 Vaccine Safety?

by Phillip M. Altman
The Brownstone Institute

In addition to Phillip M. Altman BPharm(Hons) MSc PhD, coauthors on this piece include James Rowe BPharm, MSc, PhD FRSN, Wendy Hoy AO FAA FRACP, Gerry Brady  MBBS, Astrid Lefringhausen, PhD, Robyn Cosford MBBS(Hons) FACNEM FASLM, and Bruce Wauchope MBBS – DTM&H, Dip OBS RACOG, FRACGP.

The US Department of Defense (US DoD) has had a dominant role in the response to the SARS-CoV-2 virus and in the development, and distribution of the Covid 19 vaccines, a fact hidden from the general public. In those processes many standard steps and procedures, otherwise required for pharmaceutical products, were omitted or circumvented.

Definition of these vaccines as “countermeasures” rather than therapeutic agents has permitted their expedited progression to emergency use authorisation and widespread rollouts. Many adverse consequences have been the outcome of this secret military response to a public health matter. Why are governments around the world, including Australia, planning to make further significant investments in this rushed vaccine technology driven by the US military?

Operation Warp Speed

With the US Food and Drug Administration’s Emergency Use Authorisation of the COVID-19 vaccines (FDA, 2020) and the Provisional Approval of the first COVID-19 vaccine in Australia (TGA, 2021), these agents were hailed as innovative life-saving responses by the pharmaceutical industry to a deadly global pandemic.

The development, testing and drug regulatory approval of these novel COVID-19 gene-based vaccines using messenger ribonucleic acid (mRNA) technology was said to have been done in less than one year, whereas development and approval of conventional vaccines normally takes about 10 years. (Seneff and Nigh, 2021). The public was told that this was assisted by financial support of vaccine companies by the US government under Operation Warp Speed.

The public was told that these COVID-19 gene-based vaccines were “safe and effective” (CDCa, 2022): that they would prevent infection and chances of serious illness and death from the virus, and would prevent transmission of the virus. We now know they do not prevent infection nor transmission and have not prevented a continuing high incidence of COVID-19. Furthermore they are associated with an unprecedented incidence of serious adverse events and deaths compared to any other drugs in the history of the pharmaceutical industry. (Turni and Lefringhausen 2022; Altman, 2022; CMN, 2022; Blaylock, 2022).

Based on the US CDC Vaccine Adverse Event Reporting System (VAERS), there were 1,476,227 adverse event reports associated with these “vaccines” (CDCb, 2022).  through December 2, 2022, which include 32,621 reported deaths and 185,412 hospitalizations. Furthermore, a rise in unexplained deaths has been reported around the world coincident with their introduction. In Australia, up to August 2022 there were 18,671 excess deaths (17 percent) more than average, with most of these deaths not due to COVID-19 (ABS, 2022).  We are probably facing the worst health disaster in history.

How did the pharmaceutical industry, our governments and our drug regulators get it so wrong?  A plausible answer to this question has emerged within the last few weeks.

A National Security Operation

Contrary to popular belief that pharmaceutical companies drove the COVID vaccine development programs, the US FDA’s website (FDA, 2020) reveals that the United States Department of Defence (DoD) has been in full control of the Covid Vaccine development program since its beginning. The DoD has been responsible for development, manufacturing, clinical trials, quality assurance, distribution and administration, since that time (FDA, 2020; Rees and Latypova, 2022; KEI, 2022; Medical Defense Consortium, 2022; Rees, 2022). The major pharmaceutical companies have been involved as “Project Coordination Teams” effectively performing as subcontractors to the DoD. The Chief Operating Officer for the Warp Speed vaccine program is the US Department of Defence, and the Chief Science Advisor is the US Department of Health and Human Services (HHS).

The Nature of Gene-based Vaccines

The true nature of the COVID-19 ‘vaccines’ has been largely misrepresented by mainstream media, big pharmaceutical companies and governments and is poorly understood by the population at large.  Referring to these products as “vaccines” led most people to consider them as relatively safe and well-researched and readily accept their widespread use. However, they are not really vaccines – they are serious gene-based interventions which have never been deployed widely in any population, especially never to healthy individuals including children, infants and pregnant women.  In this sense they should be considered experimental.

COVID-19 ‘vaccines’ fall into a special class of therapeutic agents under the US FDA Office of Cellular, Tissue and Gene Therapies’ defined as “gene therapy products,” which involve “introducing a new or modified gene into the body to help treat a disease” (FDA, 2018). Heretofore, use of gene therapy products has been limited to the treatment of usually rare, serious and debilitating disease or genetic conditions. They have potential to cause permanent intergenerational genetic damage, cancer and interfere with reproductive capacity.

The FDA and other drug regulatory agencies have specific rules and guidelines to direct manufacturers in development and testing of such products, for both preclinical (FDA, 2013) and clinical (FDA, 2015) research.  However, the FDA did not evaluate these COVID-19 “vaccines” according to these gene therapy guidelines.

Instead, there was a concerted effort to avoid referring to them as gene therapy products, based, in part, on the argument that the genetic material in the COVID-19 vaccines was not intended to be incorporated into an individual’s DNA, nor to modify gene expression. There was no prior short-term safety information and no long-term data on which to predict future effects. No similar therapeutic products have been previously approved anywhere in the world.  Their widespread administration globally with no historical safety experience was an unprecedented risk in human health.

Accelerating Development

Messenger RNA platform technology has been researched by DARPA (Defense Advanced Projects Research Agency) since at least 2012 (McCullough, 2022).  In early 2020, in the panic to develop the COVID-19 vaccines, certain critical research and development procedures were omitted, bypassed, curtailed, or not done in a logical sequential manner, or to established laboratory or manufacturing standards. Although the spike protein is the active drug and is directly responsible for the immune response, its pharmacology and toxicology have not been studied in animals or in humans as would normally have been required.

Other notable deficiencies include lack of critical research on carcinogenicity, mutagenicity, genotoxicity and reproductive toxicology in appropriate animal species. In particular, the potential for reverse transcription of mRNA genetic material into an individual’s DNA was not investigated. Furthermore, scale-up manufacturing was premature and lacked adequate quality control to ensure that product made in large batches is the same as made in smaller batches.

Without such research, the potency, mRNA integrity, presence of contaminants and stability of the “vaccines” cannot be guaranteed. Such oversights are directly responsible for the failure to predict the serious adverse drug reactions and mortality which have now been reported in association with these vaccines. 

To mitigate risk, the plan in vaccine development was to use multiple technologies, multiple facilities and redundancy. Leverage of existing facilities would also take place. In the interest of expediency, the plan was to avoid using traditional pathways from early development to large-scale production.  Avoidance of quality standards and guidelines such as Good Manufacturing Practice and Good Laboratory Practice guidelines was necessary to speed development, and conventional New Drug Application (NDA) and Biologics License Application (BLA) approvals were bypassed.

Instead, the process moved rapidly using compressed timelines and overlapping stages of development towards Emergency Use Authorization (EUA). Scale-up and large volume manufacturing was planned in parallel with, instead of before, clinical trials which, again, may have contravened accepted codes of Good Manufacturing Practices. These approaches were probably a recipe for potential disaster. (Latypova, 2022; Watt and Latypova, 2022).

Key legislative elements enable the US government to authorise, fund, contract and control many DoD research programs, as follows:

  • the Emergency Use Authorisation regulations (1997) allow, in cases of emergency, a new drug to be made available with less supportive safety and efficacy data than normally required for full approval.
  • the Other Transaction Authority regulations (2015) permit contractual transactions that are not required to comply with Federal laws and regulations, and
  • the Public Readiness and Emergency Preparedness Act (PREP Act 2020) establishes limited liability for the companies involved in the contract arrangements with the DoD.

Two US DoD agencies, the Defense Advanced Research Projects Agency (DARPA) and the Biomedical Advanced Research and Development Authority (BARDA), possess considerable resources for research, development and approval for various products. They also contract with a large number of companies for such functions.

The products of these programs, including the COVID-19 vaccines, are sometimes classified as “countermeasures,” “prototypes,” or “demonstrations” rather than pharmaceutical products. Those labels permit a product to avoid lengthy conventional regulatory, commercial development and testing pathways normally required for pharmaceutical products (ICH, 2022) and to proceed to Emergency Use Authorization.

The Rush to Large-Scale Manufacture

The rush to make available the Covid vaccines has reportedly led to batch-to-batch variability, with some batches associated with a high incidence of adverse vaccine reactions and mortality (Gutschi, 2022). In addition, at least 26 researchers/research teams in 16 countries, using various microscopic methods of analysis, have reported the presence of undeclared microscopic geometric and tube-like structures in both the Covid vaccine vials, and in the blood of people in widely vaccinated populations, for which there is no satisfactory explanation at this time. Furthermore, various spectroscopic methods of analysis have detected the presence of undeclared and unexpected metals (German Working Group, 2022; Hughes, 2022).

Under normal circumstances, even a tiny fraction of the reported quality, efficacy or safety problems associated with the Covid vaccines would have led to their immediate withdrawal, but this has not happened. Pharmaceutical regulators globally seem to be willfully blind to the problems. Governments and the mainstream media appear to show no interest in uncovering the truth or conducting a public debate on these critical matters. Why?

The answer appears to be that, in the interest of national security, the US DoD took charge of the Covid vaccine funding, development and testing from the very start of the perceived threat in early 2020. In the early panic, normal prudent quality, safety and efficacy considerations were compromised. Drug regulators played, and continue to play, an acquiescent role in approving and endorsing these vaccines. We now see this was a mistake. Many are now of the opinion that the Covid vaccines appear to have done more harm than good (Dopp and Seneff, 2022). Uncovering the truth has been a slow and arduous process, which has been exacerbated by the intense and unprecedented censorship of doctors and scientists, which continues to this day.

Conclusion

Many questions have arisen about the COVID vaccines concerning the lack of adequate manufacturing practices, quality control, basic pharmacological and toxicological studies and the lack of appropriate clinical safety and efficacy studies. Drug regulatory authorities seem reluctant to acknowledge the unprecedented level of reported serious adverse drug reactions and deaths associated with these products. There is also serious concern regarding the increases in excess deaths from all causes in many countries suspiciously with their use. Our health authorities steadfastly refuse to consider that the vaccines themselves may be to blame.

The public was told these COVID vaccines were “safe and effective” without qualification even though they were not fully approved. Why was the public not advised that the normal standards of quality, safety and efficacy were not applied to the development and testing of these vaccines? Why was this kept secret? Why are governments around the world, including Australia, planning to make further significant investments in this unsafe vaccine technology? Will these national security arrangements still be in place for future vaccines and other pharmaceutical products?

The fate of humanity and all future generations is literally at a critical tipping point and few global power brokers and political decision-makers appear to realise the gravity of the situation.

References

  • Altman P, Rowe J, Hoy WE, Brady G, Lefringhausen A, Cosford R, Wauchope B. Did National Security Imperatives Compromise Covid-19 Vaccine Safety?

Read the full article at The Brownstone Institute.

Category:

Activism, vaccines, Viruses

Wrongful Death – Agent Remdesivir

**UPDATE**

Stories continue to pour in on how patients drive to the hospital but leave in body bags due to the ineffective, brutal,  deadly but government subsidized COVID hospital protocols which made people prisoners and actually outright killed people.

https://joeygilbert.substack.com/p/wrongful-death-agent-remdesivir

Wrongful Death – Agent Remdesivir.

“Be not afraid, but speak and don’t keep silent.” Acts 18:9

Joey Gilbert (Attorney)

On December 27, 2022, my colleague and I filed our second Remdesivir Wrongful Death Lawsuit here in the State of Nevada, where we alleged that a Las Vegas hospital and its staff violated Nevada law, medical ethics, acted with negligence, and were motivated by financial incentives in their treatment of patients with COVID-19.

In November of 2020, a Nevada woman developed COVID-19 and was transported to the hospital with mild symptoms.  After providing their medical diagnosis, the physicians admitted her to a general medical room and placed her on a Bi-Pap machine to assist with her breathing.  Everything was normal for her on November 23.  For reasons unknown, those physicians started her on a 4-day course of the deadly drug Remdesivir.  (See link for article)

__________________

Summary:

  • After being stabilized, for reasons unknown, they weaned her off the Bi-Pap machine and moved her into ICU.
  • Despite being stabilized, physicians intubated her because of ‘respiratory failure.’
  • Four days after her Remdesivir treatment she developed seizures, went into hypotensive shock with renal failure, and subsequently died.
  • Remdesivir has a frightening history and was pulled from a controlled trial for Ebola due to high death rates (53%).
    • Remdesivir is ineffective
    • Remdesivir is toxic and causes kidney poisoning, fluid in the lungs, organ damage, and death
    • Remdesivir received EUA designation in 2020 for COVID by the NIH panel, of which 9 had financial ties to Gilead Sciences – Remdesivir’s manufacturer.
  • Under EUA designation, a product can not be mandated by law.  Patients must provide consent including the fact:
    • they have a 99.7% chance of surviving COVID without it
    • their odds of dying increases exponentially if it is administered
    • odds of survival decrease exponentially when Remdesivir is combined with intubation
  • In this case, neither the patient nor the family were advised of or provided with this information
  • The patient was given Remdesivir as part of a protocol which enriched the hospital financially, affecting their professional judgement, yet hurt the patient
  • It is a violation of Nevada law to administer unnecessary medical treatment and without consent
  • Patients coming to the hospital are:
    • separated from family
    • declared to be in ICU even when they are not
    • told Remdesivir is the only available and safe treatment
    • told if they leave the hospital “against medical advice” their insurance will be voided
    • placed on a Bi-Pap machine at a high rate, making it difficult to breathe, and have their hands tied down so they can’t take it off their face
    • deemed “agitated” by a psychiatrist if they struggle and are placed on morphine
    • given Remdesivir, Benedryl, and Tylenol which dry out their lungs which overloads their kidneys and are denied food and water
    • often intubated and placed on other drugs that are contraindicated for use with Remdesivir
    • left to die, which on average takes about nine days
    • The state of Nevada received $1 BILLION from the CARES Act
      • $241 MILLION in direct cash payments were distributed to Medicare providers
      • $88 MILLION was given in grant funding from CDC to be used for enhanced testing and contact tracing
      • $70 MILLION was distributed to health care providers and community health services to address costs associated with the pandemic
  • Hospitals can charge THREE different rates for COVID diagnosed patients (which have varied between 2020-2022)
    • $3,200 per out patient
    • $111,213 per in patient (noncomplex)
    • $461,780 per patient (complex) 
    • All that is required to move a patient from noncomplex to complex is to be intubated or placed in ICU status
    • Medicare has provided a code that permits a 20% NCTAP bonus, collected on the entire bill, distributed to hospitals who offer Remdesivir as an exclusive option

_________________

For more:

Category:

Activism, Treatment, Viruses

Lyme Literate Docs Needed in Pennsylvania

https://www.lymedisease.org/ilads-pa-lyme-conf-march-24-25/

Inform your doctors about ILADS/PA Lyme conference March 24-25

PA Lyme resource network

A Message from PA Lyme Resource Network

We need your help!

Pennsylvania urgently needs more Lyme-literate healthcare practitioners.  We’ve been the #1 state for instances of Lyme disease and tick-borne illness for seven consecutive years, yet we’re losing more LLMDs than we’re gaining.

Working to change that, we’re partnering with ILADS to bring an important Lyme & Tick-Borne Disease Medical Conference to Hershey, PA on March 24-25.

The more doctors and medical practitioners we can bring to the conference, the better for our Pennsylvania communities. This is why we’re asking you to personally invite your primary care practitioner and any other doctors you can reach.

Ways to take action:

About ILADS

About PA Lyme Resources Network

Category:

Activism, Lyme