Archive for the ‘Treatment’ Category

Medical Board and Health System Schooled By Drs. Nass and McCullough

https://childrenshealthdefense.org/defender/meryl-nass-license-suspension-maine-medical-board-hearing

Witness Forced to Walk Back Accusations That Led Maine Medical Board to Suspend Dr. Meryl Nass’ License

The Maine Board of Licensure in Medicine on Tuesday called two witnesses to testify in its third hearing on the suspension of Dr. Meryl Nass over her treatment of patients with COVID-19. Under cross-examination, the first witness was forced to walk back many of his claims.

The Maine Board of Licensure in Medicine on Tuesday held its third hearing on the suspension of Dr. Meryl Nass related to her treatment recommendations for patients with COVID-19.

As it did on day two of the hearings, held on Oct. 27, 2022, the board focused on Nass’ alleged “sloppy” record-keeping for three patients she treated and on her prescribing of ivermectin and hydroxychloroquine for those patients.

The board suspended Nass, a member of the Children’s Health Defense scientific advisory board, on Jan. 12, 2022, without a hearing.

The board initially accused Nass of “unprofessional” and “disruptive” behavior, spreading “misinformation” and prescribing hydroxychloroquine and a “deworming medication” (ivermectin) to patients.

However, the board withdrew the accusations of “misinformation” on Sept. 26, 2022, just prior to her first hearing date, Oct. 11, 2022.

The board’s case now rests on Nass’ alleged non-adherence to the medical “standard of care” as it pertained to ivermectin and hydroxychloroquine for treating COVID-19 and on the alleged “record-keeping” issues.  (See link for article)

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**Comment**

This, right here, should concern everyone.  It again deals with “consensus” based medicine where dictates come from the top and go down to doctors who are nothing more than government soldiers who simply must obey orders.  Thinking folk need not apply.  The following quote by Nass says it all:

“Doctor Courtney doesn’t read journal articles,” Nass wrote. “He sticks by the recommendations of government agencies and his specialty organization, the Infectious Diseases Society of America (IDSA).”

The IDSA was sued by the State of Connecticut “for denying the existence of chronic Lyme disease.”

This issue matters because it directly relates to the ongoing conundrum in Lymeland where there are two camps of thought.

Nass isn’t out of the woods yet and the next hearing is set for March 2.

https://popularrationalism.substack.com/p/the-wellness-companys-dr-peter-mccullough

The Wellness Company’s Dr. Peter McCullough Has Been Vindicated in Court

Baylor Scott and White Lawsuit Against Dr. McCullough Dismissed

MIAMI, Feb. 1, 2023 (PRNewswire)

A 2021 lawsuit filed by Baylor Scott and White Health system against world-renowned internist, cardiologist, and COVID-19 expert Dr. Peter A. McCullough, MD, MPH, has been dismissed by the 191st Judicial District Court, Dallas County, Texas. Associate Judge Tahira Khan Merritt granted the nonsuit and dismissed with prejudice all claims asserted or that could have been asserted in the case. Dr. McCullough stated,

“This is a strong victory for freedom of speech and fair balanced publication and media presentation of clinical data as it has emerged over the course of the pandemic crisis. My analyses and conclusions have been accurate, consistent, and have always been my own, not those of any institution.”

(See link for article)

Doctors who treat Lyme/MSIDS have been going through this crucifixion for decades.  Now, those who dare to use their God-given brains regarding COVID are also being hunted down and persecuted.  The monopolization of medicine is nearly complete.  Unless we speak out we will find ourselves stuck in a paradigm that will not allow Lyme/MSIDS patients ANY appropriate treatment whatsoever.

For more:

Patient Contracts Babesia From a Blood Donor: Only 14 States Test For It

https://danielcameronmd.com/patient-contracts-babesia-blood-donor/

PATIENT CONTRACTS BABESIA FROM A BLOOD DONOR

babesia-blood-donor

Babesia is most commonly transmitted through a tick bite but it can also be transmitted through a blood transfusion. To minimize the risk to the public, blood banks now screen donors for Babesia in endemic states.

In their article “Transfusion-transmitted babesiosis in a patient with sickle cell disease undergoing chronic red cell exchange,” Costa and colleagues describe a patient who contracted Babesia from a donor living in Ohio, a state that is not considered endemic for Babesia

According to the authors, a 30-year-old man with sickle cell disease (SCD) required approximately 10 units of red blood cells every 3–4 weeks throughout his childhood.

Approximately 2 months after a red blood cell exchange, he presented with fever, neck pain, and photophobia. Several days later, he developed a persistent fever, chills, headache, fatigue, and loss of appetite.

He was diagnosed with Babesia through identification of parasites in his red blood cells and positive antibodies. He was also borderline positive on an antibody test for Anaplasma phagocytophilum and Ehrlichia chaffeensis.

“Prior to laboratory-based blood donor screening for Babesia, transfusion-transmitted babesiosis (TTB) was a leading infectious risk to the blood supply in the United States.”

The young man was treated for Babesia with azithromycin and atovaquone for 10 days with resolution of his symptoms. He was not treated for Anaplasma phagocytophilum or Ehrlichia chaffeensis.

The patient lived in a state endemic for Babesia but did not recall a tick bite.

“A donor lookback investigation was initiated with the blood supplier,” the authors wrote. They found that in the preceding 6 months, the patient had received 65 units of blood, with 58 units screened for Babesia.

Unfortunately, “One of the donors of the 7 untested units was B. microti seropositive,” the authors wrote. The donor lived in a state not requiring Babesia screening.

“Our case demonstrates the continued vulnerability of the US blood supply to Babesia.”

“The seropositive donor had not had any symptoms of babesiosis; he lived in Ohio and reported being very active over the past year, including hiking and camping in several states (Ohio, Tennessee, and North Carolina),” the authors wrote.

In 2019, the FDA recommended testing of blood donors for Babesia in the 14 states where almost all cases of Babesia have been reported. “The policy confined to 14 states (Connecticut, Delaware, Maine, Maryland, Massachusetts, Minnesota, New Hampshire, New Jersey, New York, Pennsylvania, Rhode Island, Vermont, Virginia, Wisconsin),” wrote the authors.

Authors Conclude:

“Heightened awareness and health care provider education are imperative, especially in non-endemic [states] where clinicians may not be accustomed to diagnosing community-acquired or TTB, placing transfusion recipients at risk of delayed diagnosis and severe disease.

References:
  1. Costa V, Mercure-Corriveau N, Gourneau J, et al. Transfusion-transmitted babesiosis in a patient with sickle cell disease undergoing chronic red cell exchange. Transfusion. Jan 13 2023;doi:10.1111/trf.17244

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**Comment**

Once again, the madness of limiting potential infection to certain geographical areas despite the ability of people, animals, and bugs to move around is completely asinine.  Yet, here we are – still in the madness.

For more:

You Are Not Ready for This: Up to 70% of COVID Deaths Due to Ventilators

**UPDATE May, 2023**

Now a study proves that most COVID patients who died in hospitals were actually killed by the ventilators.  

https://popularrationalism.substack.com/p/you-are-not-ready-for-this-did-protocolists?

You are Not Ready for This: Did Protocolists Euthanize COVID-19 Patients with Ventilators and Sedatives “To Save Other Patients”, >50% kill rate? Up to 70% of COVID-19 Deaths Due to Ventilators

Now that the vaccinated are dominating those hospitalized, “Guidelines are just guidelines”. Please share this article and tag an AG for maximum impact. They cannot ever be allowed to do this again

TRIGGER ALERT: If you lost a loved one to COVID-19 and the doctors tried to ventilate your loved one early, please do not read any further. Have someone close to you read this, read the full article, and describe the article to you in a calm, quiet setting. You will need a friend to help you through this.

If you are a doctor who has been persecuted for doing the right thing, perhaps you lost your license or it is being threatened, send this Wall Street Journal to your lawyers – and thank you for not acquiescing to the demands that you kill patients on ventilators and with strong sedatives.

Either way, I encourage PR readers to read the WSJ article yourself and see if you agree or disagree. Leave a comment on your take. Am I wrong?

WSJ Article: McCullough, Kory, Lyons-Weiler, and Others Were Right.

In a jaw-dropping article published by the Wall Street Journal, (Hospitals Retreat From Early Covid Treatment and Return to Basics) physicians admit to ventilating patients who did not need it as a step in their protocol – get this – not as a treatment that was likely to benefit the patient, but rather as a fruitless and callous way of attempting to stop the spread of COVID-19.

“Last spring, with less known about the disease, doctors often pre-emptively put patients on ventilators or gave powerful sedatives largely abandoned in recent years. The aim was to save the seriously ill and protect hospital staff from Covid-19.

Now hospital treatment for the most critically ill looks more like it did before the pandemic. Doctors hold off longer before placing patients on ventilators. Patients get less powerful sedatives, with doctors checking more frequently to see if they can halt the drugs entirely and dialing back how much air ventilators push into patients’ lungs with each breath.

We were intubating sick patients very early. Not for the patients’ benefit, but to control the epidemic and to save other patients,” Dr. Iwashyna said “That felt awful.”

Yes, euthanizing humans is illegal. Especially for the benefit of other patients. It should feel awful.

“Last spring, doctors put patients on ventilators partly to limit contagion at a time when it was less clear how the virus spread when protective masks and gowns were in short supply. Doctors could have employed other kinds of breathing support devices that don’t require risky sedation, but early reports suggested patients using them could spray dangerous amounts of virus into the air, said Theodore Iwashyna, a critical-care physician at University of Michigan and Department of Veterans Affairs hospitals in Ann Arbor, Mich.”

“Subsequent research found the alternative devices to ventilators, such as delivering oxygen through nasal tubes, weren’t as risky to caretakers as believed. Doctors also gained experience with Covid-19 patients, learning to spot signs of who might suddenly turn seriously ill, some said.”

The WSJ article describes a study conducted that now allows doctors to predict who needs a ventilator and who does not:

“It found more doctors now follow the pre-pandemic protocols, which have reduced the number of deaths and shortened the time patients spend on ventilators, HCA’s chief medical officer said.”

“Before the pandemic, between about 30% to more than 40% of ventilator patients died, according to research. Numbers were sharply higher in the pandemic’s early hot spot in Wuhan, China. As the pandemic grew, hospitals in the U.S. reported death rates in some cases of about 50% for ventilated Covid-19 patients.

(25.6 – 7.6)/25.6 = 70% of COVID-19 Deaths Due to Ventilators? Up to 50% Who Died in Hospital Did Not Have COVID-19?

“One study of three New York City hospitals found the death rate for all Covid-19 patients dropped to 7.6% from 25.6% between March and August after accounting for younger, healthier patients in the summer. Hospitals in New York were less crowded in August than during the April surge, which could increase mortality, the study’s authors wrote in October in the Journal of Hospital Medicine. The study also suggests patients may have benefited from new medications and improved treatment, they said.”

Add to the fact that up to 50 percent of COVID-19 “cases” were just “PCR positive” false positives. This means under protocolists’ “care”, perhaps as many as 50% of people who died with a PCR positive test result died because of a false positive PCR test. They either never had COVID-19, or they became infected in the hospital after going home for ten days with a respiratory ailment other than COVID-19 that, if tended to properly with outpatient care, would never have led to hospitalization.

Perverse Incentives to Ventilate Patients.

In a remarkable rarity of “fact-checking” gone right during the heyday of COVID-19 disinformation, USA Today actually verified Dr. Scott Jensen’s reports that hospitals were receiving financial incentives that he considered “gaming the system”, citing numerous independent so-called fact-checker opinion websites.

“We rate the claim that hospitals get paid more if patients are listed as COVID-19 and on ventilators as TRUE”, they reported in April, 2020.

Hospitals and doctors do get paid more for Medicare patients diagnosed with COVID-19 or if it’s considered presumed (sic) they have COVID-19 absent a laboratory-confirmed test, and three times more if the patients are placed on a ventilator to cover the cost of care and loss of business resulting from a shift in focus to treat COVID-19 cases.”

It’s REAL Early Treatment, Stupid

We were right. So many of us were right. Protocolists should have listened.

Who Are the World’s Leading Authorities in COVID-19 Treatment?

Immeasurably Callous: Now That the Vaccinated Are Being Hospitalized Far More,“Guidelines are just guidelines”

From the WSJ article: “Researchers and doctors continue to study Covid-19 patients who require ventilators, and some experts have called for flexibility from pre-pandemic standards for doctors to decide how to calibrate ventilators. ‘It’s personalization, that’s the key word,’ said John Marini, a professor of medicine at the University of Minnesota. ‘Guidelines are just guidelines.’”

Anyone paying attention to the Public Health takeover of allopathy understands the reality that guidelines are only guidelines until someone in HHS or the White House decides to shut you down on personalized medicine.

We need harsh, hard investigations with consequences – and activists need to write bills tying the hands of protocolists to prevent them from ever again killing one patient to hypothetically save another – under threat of a murder charge.

We need legislation for “on-demand” scripts for off-label medicines that patients want for potentially deadly infections – regardless of “FDA Approval” (FDA does not, by definition, have to “approve” off-label scripts.

Also: there are helmet-based ventilator options – that are far less invasive, patients do not feel they are being attacked or strangled – and they come with free training.

Please let others know that hospitalists and protocolists have confessed to murder. Tag an attorney general in your post

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**Comment**

The WSJ article was written in Dec. 2020, and unfortunately, the supposed retreat and “return to basics” isn’t happening – at least where I live.  Mainstream doctors are still choosing lucrative protocols over individualized care, still utilizing toxic remdesivir, and still denying life-saving, cheap drugs like HCQ and ivermectin.  Politics and money are still leading science as evidenced by the continued push for the clot-shots despite not preventing transmission as well as all the evidence they are killing and maiming people. 

A new RCT; however, shows that ivermectin (200 microgram/kg) on day 1, followed by 100 micrograms/kg daily from days 2-28 in completely unvaccinated people reduces transmission by 72% The clot shots failed.  Ivermectin works at every stage of COVID, (and some 20 other viruses) but the band plays on.

Perfect Timing! mRNA Treatment in Pipeline to Inject Straight Into Hearts of Those Suffering Heart Issues After COVID Shots

**UPDATE**

Dr. Michael Yeadon in this video states that companies are now remanufacturing every old vaccine into the mRNA platform and that there are written contracts with governments for 10 shots per citizen which the body can’t withstand.

Moderna’s products just keep rolling off the assembly line.  The company states its mRNA RSV “vaccine” is “effective.” It plans to file a request for approval from the FDA yet this year.  Pfizer submitted a request for expedited review of its mRNA version of an RSV vaccine for older adults last December.  And several new government and industry-funded studies are underway to develop mRNA “vaccines” for livestock.  The gravy-train for mRNA products is running full steam ahead and includes a new flu shot, an annual COVID shot, a shot to “prevent” RSV in bovines, a COVID shot for zoo animals, as well as black-footed ferrets, and third-generation “vaccines” for pets and wild animals.

All this despite many experts stating mRNA products are unstable and circulate systemically via the blood, causing cells to take up messenger RNA which is expressing a foreign new antigen throughout the body.  The body sees this foreign new antigen as an invader – like an autoimmune disease.

  • It has never been proven that mRNA genetic therapy injections are any better than previous vaccines.
  • The amount of antigen can not be controlled in the mRNA platform.
  • The mRNA platform creates systemic autoimmune disease.
  • Due to reverse transcriptase (an enzyme within our cells), the implications are unknown if the mRNA platform could produce a potential cancer risk or transgenerational expression.
  • mRNA vaccines, besides the current diabolical experiment with the COVID shot, have “NEVER been effectively been put into humans before, except one or two where it didn’t work very well. This is a massive experiment. The vaccines are actually registered as experimental vaccines. ~ Professor Robert Clancy

https://childrenshealthdefense.org/defender/moderna-mrna-heart-failure/

‘Science Fiction Medicine’: Moderna Developing mRNA Injection to Treat Heart Failure

In a Jan. 9 update on the company’s “industry-leading mRNA pipeline,” Moderna told investors it is developing multiple new mRNA products — including a treatment designed to be injected directly into the hearts of patients who have sustained heart attacks or heart failure.

Moderna raked in significant earnings in 2022, based on $18.4 billion in sales of its mRNA COVID-19 vaccine — the company’s one and only product on the market.

But in a Jan. 9 update on the company’s “industry-leading mRNA pipeline,” Moderna told investors it is developing multiple new mRNA products — including a treatment designed to be injected directly into the hearts of patients who have sustained heart attacks or heart failure. (See link for article)

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**Comment**

How conveniently timely.

SUMMARY:

  • Clinical trials are in Poland and the UK.
  • “It’s a bit like science fiction medicine but that’s what is really exciting to me.” ~ Stéphane Bancel, Moderna CEO
  • Moderna has a long history of failure. Pfizer has a long history of fraud.
  • Like the COVID shots, there is no safety track record for this type of genetic therapy
  • “There is no safety track record for genetic therapies that introduce functional code for production of a protein for an uncontrolled quantity and uncontrolled duration of time. There are no assurances on long-term safety of mRNA technology.” ~ Dr. Peter McCullough, Cardiologist and immunologist
  • “In short, Moderna will fix the problem it created.” ~ The Gateway Pundit
  • Moderna has 48 programs in development including 36 in clinical studies with:
    • flu
    • RSV
    • cytomegalovirus
    • cystic fibrosis (inhalable mRNA therapy)
    • personalized cancer “vaccine”
  • Moderna also has acquired OriCiro Genomics (specializes in cell-free synthesis and amplification of plasmid DNA, a key building block of mRNA manufacturing). 
  • Moderna has a collaboration with CytomX Therapeutics for the development of mRNA-based therapeutics for cancer.
  • Moderna has an ongoing partnership with Metagenomi, funded by Bayer which acquired Monsanto, to accelerate development of in vivo gene editing therapeutics.

mRNA technology is the new golden calf, cash cow of Big Pharma and our corrupt government.  Researchers have been working on it for decades with ZERO success until COVID when it was rammed forward under Emergency Use Authorization (EUA), with much less scrutiny/testing than usual. All you have to do is look around at the carnage to see it is unsafe due to antibody dependent enhancement (ADE) and the unbelievably high rate of adverse events.

Tick-borne Disease Treatment Study Proposals Needed

https://www.lymectn.org/Pilot.aspx

CTN Tick-borne Disease Pilot Treatment Study Award

We are happy to announce that the Clinical Trials Network established with a grant from the Steven & Alexandra Cohen Foundation to Columbia University announces the third round of Pilot Study Proposal submissions (January 15 to March 15, 2023).

The Clinical Trials Network welcomes clinicians, researchers, and investigators from academic institutions to submit proposals. The proposals are typically 1-3 pages in length, but longer proposals are accepted for review. The CTN’s goal is to support the conduct of small-scale human treatment studies related to treatment of Lyme and other tick-related diseases. These small pilot studies are conducted to determine whether future larger investigations are warranted. Pilot studies often assess safety and feasibility, are exploratory in nature, and are not meant to answer the same questions as larger randomized control trials.

The CTN Study Review Committee will review submissions for consideration for further development into a pilot study; each pilot study will be conducted at one of the CTN investigation sites. The CTN has funding to support 1-2 small pilot studies each year.

Current CTN network affiliates include investigators from Columbia University Irving Medical Center in New York City, Johns Hopkins University Medical Center in Baltimore Maryland, and Children’s National Hospital in Washington D.C. The CTN Study Review Committee includes the core CTN members, clinical research experts, and academic and community clinicians. Results of the CTN pilot studies – if favorable – will lead to consideration for larger Randomized Controlled Trials.

The deadline for the first round of submissions for treatment research ideas from the research scientists and clinicians is March 15, 2023. The submission period opens January 15, 2023.

We thank all clinicians and investigators in advance for participation in this process, as your proposal may lead to a transformative study.

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For more:

The fear here is that if this leads to human trials, only those who test positive with an EM rash will qualify, persistent infection will be once again denied, and the continued use of PTLDS will be utilized which will once more omit the sickest patients that are seronegative and without the rash.  This affects everything and hasn’t changed in 40 years.  The entire premise and paradigm is wrong but continues to be utilized in tick-borne disease research.