Author Archive

Florida First State to Allow Doctors to Use Off-Label Drugs for Early Treatment of COVID-19 & Recommend Against COVID Shots For Kids

https://www.theepochtimes.com/florida-first-state-to-allow-doctors-to-use-off-label-drugs-for-early-treatment-of-covid-19

Florida First State to Allow Doctors to Use Off-Label Drugs for Early Treatment of COVID-19

By Meiling Lee
March 3, 2022

Repurposed drugs that have been shown to prevent or treat COVID-19 may be prescribed by physicians, the Florida Department of Health said in its new COVID-19 guidance for health care practitioners.

The guidance, published on Feb. 24, says that health care practitioners are encouraged to provide early treatment for COVID-19 patients with federally approved generic drugs that they find to work. This is in addition to the outpatient treatments granted emergency authorization usage (EUA) for people at risk of developing a serious illness.

“When recommending COVID-19 treatment options for patients’ individualized health care needs, physicians should exercise their individual clinical judgment and expertise based on their patient’s needs and preferences,” the guidance states. “These options may include emerging treatments backed by quality evidence, with appropriate patient informed consent, including off-label use or as part of a clinical trial.”

The new guidance is an effort by Republican Gov. Ron DeSantis to offer health care practitioners protection from lawsuits. He said that it’s important for doctors to be able to have access to these drugs.  (See link for article)

__________________

SUMMARY:

  • DeSantis also paves a way for doctors to report to the Agency for Health Care Administration if their hospital prevents them from treating their patients who wish to try medications not recommended by the federal health agencies.
  • Florida is the first and only state go go against the CDC’s recommendation toget sicker.’
  • Dr. Pierre Kory, president of FLCCC states many have died needlessly and that the government’s only focus is pushing gene therapy injections. He also states effective treatments have been available for 2 years but the government is still injecting people with a 2-year old shot against a variant which is extinct.
  • Kory states the EUA antiviral drugs (Paxlovid and molnupiravir) are toxic and poisonous.
  • Further, there are concerns COVID may develop resistance to these EUA antivirals because each only attacks 1 part of the virus instead of the multifaceted approach like ivermectin.
  • An article in Nature shows the importance of an antiviral targeting a polymerase and a protease to successfully eliminate a virus.
  • Then there’s the cost issue.
    • Molnupiravir costs the government $530 for 2 pills a day for 5 days
    • Paxlovid costs the government $700 for 2 pills a day for 5 days
    • ivermectin costs as low as $30 and as high as $94 for 20 tablets
  • In an ICER report (pdf) examining the outpatient treatments for COVID-19 the authors raised concerns about the effectiveness and safety of the drugs due to lack of long-term data and lack of peer review.  Yet, the FDA issued EUA for these expensive, questionable, toxic drugs while recommending against ivermectin and still states the most effective way to limit the spread of COVID is by the gene therapy injections which don’t stop transmission or infection, keep you from being hospitalized or from dying, and have caused more adverse reactions and death than any other vaccine in the history of VAERS.

__________________

https://www.theepochtimes.com/florida-to-become-first-state-to-recommend-against-covid-19-vaccines-for-healthy-children

Florida to Become First State to Recommend Against COVID-19 Vaccines for Healthy Children

By Zachary Stieber
March 7, 2022

Florida officials on March 7 said the state would be the first to formally recommend that healthy children shouldn’t get a COVID-19 vaccine.

Dr. Joseph Ladapo, the state’s surgeon general, made the announcement during a roundtable discussion titled “The Curtain Close on COVID Theater.”

“The Florida Department of Health is going to be the first state [department] to officially recommend against the COVID-19 vaccines for healthy children,” Ladapo said.  (See link for article)

Every single state needs to pass legislation exactly like this.
Medicine needs to be decentralized.  Doctors need to be given back their power to treat patients.

But, true to form, White House press secretary Jen Psaki, who is NOT a doctor or health expert, condemned Ladapo as a “politician” who is “peddling conspiracy theories,” despite being a Harvard trained MD/PhD who has worked at NYU, UCLA, the FDA, and the University of Florida.  Psaki presents a perfect example of what Weinstein and Heying (both PhD’s) discuss in a recent video where we must get used to living in a world where things are labeled upside down (up is down, right is left, and inclusive is exclusive, etc.).  And the corrupt IDSA also accuses Florida of putting “politics over the health and safety of children.”

Doctors need to freely treat without fear of persecution. This would also help more doctors be willing to learn and willing to treat Lyme/MSIDS as well as other politicized diseases.  Regulatory agencies and public health are captured agencies that are completely corrupt. A perfect example: the AMA had no trouble when the Biden Administration gave pharmacists, dentists, optometrists, podiatrists, and even veterinarians the power to administer COVID-19 injections, with the Prep Act protecting them from lawsuits if the injected person dies or is injured, but now is complaining that Biden’s “Test to Treat” plan “flaunts patient safety and risks significant negative health outcomes,” by allowing the nations largest pharmacy chains with onsite clinics, long-term care centers, community health centers, and veterans’ health centers to dispense anti-virals to people who test positive. They are all of a sudden worried about a patient’s medical history for treatment but don’t give a fig about considering this same medical history for experimental injections that have caused more adverse events and death than any vaccine in the history of VAERS.  Anyone else smell a rat?  The antivirals; however, will not be ivermectin or HCQ, but FDA “approved” drugs by Pfizer and Merck, which have 6 pages of drug interactions and use restrictions, not to mention are expensive. When listening to both sides it becomes evident that behind it all is a power grab with a lot of money involved.  Once again, patients are way down the priority list.

Wisconsinites: Action Needed for AB 316 – Prohibit Discrimination Based on Vaccination Status

Dear Wisconsin NVIC Advocacy Team Members,

You have the opportunity to support a good bill, AB 316,  which would prohibit governmental entities in Wisconsin from discriminating against individuals based on their COVID-19 vaccination status or whether they have proof of receiving a COVID-19 vaccine. AB 316 is on the Senate Calendar for Tuesday, March 8th, 2022. 

ACTION NEEDED:

1) Contact your Wisconsin State Senator and ask him or her to vote in favor of AB 316! Please see talking points below. If you do not know who your Wisconsin state senator is, login to the NVIC Advocacy Portal at http://NVICAdvocacy.org. Click on “Who Represents Me” on the home page or “My State” on the STATE TEAMS tab. Your personal state legislators are listed on the bottom of the page. You can click on your legislators’ names to get phone numbers, emails, and even links to their social media to connect to them. You can also find your state senator at this link: https://maps.legis.wisconsin.gov/

2) Please share this email with family and friends, or you can tell them to go to http://NVICAdvocacy.org and click on the alert for Wisconsin AB 316.

3) Login to the NVIC Advocacy Portal OFTEN to check for updates.  http://NVICAdvocacy.org. We review bills and make updates daily. Bills can change many times over the legislative process and your timely visits, calls, and emails directed at the correct legislators are critical to this process.

TALKING POINTS (Please personalize to share how this bill affects you and your family):

  • AB 316 would prohibit discrimination based on COVID-19 vaccination status by the state and other governmental entities in Wisconsin.
  • Any form of discrimination against individuals unvaccinated against COVID-19 is essentially a form of coercion to try and get them vaccinated by implementing barriers to navigate life.
  • It is unreasonable to penalize perfectly healthy individuals who simply have not received a particular vaccine.
  • This bill would prohibit government-sponsored COVID-19 vaccine discrimination, allowing residents of Wisconsin to freely participate with their state and local governments.
  • It would also ensure that the residents of Wisconsin are allowed to access needed state and local government facilities and services without fear of discrimination based on their COVID-19 vaccination status.
  • State and local governments are taxpayer-funded and exist to serve the public. Since there is no vaccine requirement for paying taxes, there should be no chance of a vaccine requirement for accessing or using government facilities and services, or as a prerequisite for any other type of interaction with the government.
  • Passing this bill would also clarify that there is no state requirement or expectation of private persons and entities in Wisconsin to mandate COVID-19 vaccines or to require proof of vaccination.
  • Even individuals who are vaccinated against COVID-19 can still spread and catch it. COVID-19 vaccine requirements or mandates reduce the focus from health to mere vaccine status.
  • Our American system of government was founded upon protecting the rights of individuals. This protection entails prohibiting the intrusion upon these rights from other individuals and entities, including the government itself.

Sincerely,

NVIC Advocacy Team
National Vaccine Information Center
http://NVIC.org and http://NVICAdvocacy.org
https://nvicadvocacy.org/members/Members/ContactUs.aspx

Make A Difference, support NVIC. NVIC is a certified 501(c)3 Charity.

The National Vaccine Information Center (NVIC) works diligently to prepare and disseminate our legislative advocacy action alerts and supporting materials.  We request that organizations and members of the public forward our alerts in their original form to assure consistent and accurate messaging and effective action. Please acknowledge NVIC as originators of this work when forwarding to members of the public and like-minded organizations. To receive alerts immediately, register  at http://NVICAdvocacy.org, a website dedicated to this sole purpose and provided as a free public service by NVIC. 

For a rousing pro-medical freedom, anti-segregation speech by a civil rights attorney who flatly states “vaccine” mandates are illegal and a form of medical rape:  https://rumble.com/vs33yz-tricia-lindsay.html

Case Review: 80 Year Old With Lyme Encephalopathy Instead of Dementia

https://danielcameronmd.com/case-review-80-year-old-lyme-encephalopathy-instead-dementia/

Case review: 80-year-old with Lyme encephalopathy instead of dementia

lyme-encephalopathy

“An 80-year-old patient was admitted to the hospital after a fall, and subsequently developed an acute confused state requiring transfer to a neuropsychiatric unit,” writes Karrasch and colleagues in the journal Ticks and Tick-borne Diseases. [1]

“While mostly vigilant and awake, he intermittently lacked full orientation, had reduced attention, concentration, short-term memory function, increased motor activity, mild formal thought disorder (incl. some tangential thinking), but no frank psychotic symptoms,” the authors explain.

The man was diagnosed with delirium, potentially related to dementia. An abnormal F18-FDG-PET scan was interpreted as consistent with early Alzheimer’s disease. And memantine was prescribed.

However, the patient remained confused, despite receiving the antipsychotic medication risperidon and pipamperone for sleep disturbances. “The patient lacked orientation, had recurrent pervasive disturbances of sleep-wake-cycles, was intermittently restless, and also incontinent,” states Karrasch.

The patient’s spinal tap revealed an increased protein, lymphocytic pleocytosis of 260 leucocytes/μl, intrathecal IgM-synthesis, and elevated lactate. “The lymphocytic pleocytosis with signs of activation together with the dominance of intrathecal IgM-synthesis raised the differential diagnosis of neuroborreliosis,” writes Karrasch.

He also had an elevation of the chemokine CXCL13. And while this is not yet validated as a routine diagnostic tool, CSF [cerebrospinal fluid] CXCL13 may be another option to increase sensitivity and accuracy in diagnosing Neuroborreliosis, next to CSF lymphocytic pleocytosis, explains Karrasch.

The patient was given a 21-day course of ceftriaxone. As a result, his confusion and delirious symptoms resolved.

The man was “dismissed from the hospital in a clearly improved clinical status,” writes Karrasch, “despite an additional complication of aspiration pneumonia.”

The authors point out their case report demonstrates the possibility that confusion or acute encephalopathy can be a presenting feature of neuroborreliosis and that CXCL13 may be useful as a biomarker in central nervous system manifestations of Lyme borreliosis.

It is fortunate the doctors were able to recognize neuroborreliosis and successfully treat the 80-year-old man, or he might have been misdiagnosed with dementia.

References:
  1. Matthias Karrasch, Volker Fingerle, Katharina Boden, Andreas Darr, Michael Baier, Eberhard Straube, Igor Nenadic, Neuroborreliosis and acute encephalopathy: The use of CXCL13 as a biomarker in CNS manifestations of Lyme borreliosis, Ticks and Tick-borne Diseases, Volume 9, Issue 2, 2018, Pages 415-417, ISSN 1877-959X, https://doi.org/10.1016/j.ttbdis.2017.12.008.

___________________

**Comment**

It is highly likely this man will relapse and need further treatment; however, this topic is purposely avoided by the ‘powers that be’ as that would put direct salvos through their accepted narrative that a few weeks of antibiotics cures this.

How many more are walking around diagnosed with dementia, Alzheimer’s, MS, and other neurological labels when they have undiagnosed Lyme/MSIDS?

For more:

Former WHO Consultant Exposes Ivermectin Takedown

Again, Lyme/MSIDS patients need to understand that when corrupt public health authorities and governmental agencies censor and ban what they consider ‘misinformation,’ patients will be negatively impacted as dissenting opinions will not be allowed.  This has happened for 40 years in Lymeland and now is being seen in COVID. The following information is an important lesson that is imperative to know or we will find ourselves without any help whatsoever from medicine.  As it is, we must find Lyme literate doctors (LLMDs) who defy the accepted narrative that Lyme is hard to catch, and easy to treat and that uses abysmal testing that misses nearly everyone, leaving thousands upon thousands to suffer in silence.  Please share this info widely so people are educated on what is happening.

https://thehighwire.com/videos/former-w-h-o-consultant-exposes-takedown-of-ivermectin/  Video Here (Approx 55 Min)

FORMER W.H.O. CONSULTANT EXPOSES TAKEDOWN OF IVERMECTIN

Del sits down for a one-on-one with the former W.H.O. consultant & research scientist, Tess Lawrie MD, PhD, who was a critical part of the Ivermectin trials over a year ago with overwhelmingly positive conclusions. See data and recorded personal zoom calls that reveal how a key review was attacked from within, keeping the safe, life-saving drug out of the hands of millions of dying Covid patients for more than a year.
This is a mind-blowing expose on how Ivermectin was covered up. There have been too many scenarios, just like this one, where a well-meaning doctor or scientist appears to be doing the right thing, trying to show the truth about the efficacy (or non-efficacy) of a drug, until suddenly, they start acting very strangely, they are no longer being ethical, and won’t admit why.  Money and coercion are typically at the root of these scenarios, and sadly, this is just one more case where – what do you know – as it turns out, The Gates Foundation seems to have been one of the major factors in this cover-up.  Source  (I highly recommend utilizing this sourcelink as there is a plethora of information within it including interviews and data.)
For more:

Poison Control Centers Warn About Toxic Chemical in At-Home Virus Test Kits, Children at Higher Risk & FDA Warns of False Results

https://www.theepochtimes.com/facts-matter-feb-28-poison-control-centers-warn-about-toxic-chemical-in-at-home-virus-test-kits-children-at-higher-  Video Here

Poison Control Centers Warn About Toxic Chemical in At-Home Virus Test Kits, Children At Higher Risk

Facts Matter

Feb. 28, 2022

Roman Balmakov

The National Poison Control Center, in a new official statement, is warning Americans of a toxic chemical that was found to be present in at-home COVID-19 test kits—specifically, in the test kits being sent out by the U.S. government to households across America. (See link for article)

____________________

Highlights:

  • The test kits are made in China.
  • The toxic ingredient is sodium azide, which is used as a preservative, propellant in automobile airbags, herbicides, and in pest control agents.
  • Sodium azide, when swallowed can cause low blood pressure, dizziness, headache, and heart palpitations, but in more severe cases, seizures, loss of consciousness, and DEATH may occur.  It is considered a very potent POISON.
  • If it is put on skin it can cause irritation or chemical burns. It can cause nostril irritation.
  • Numerous test kits contain this chemical: BinaxNow, BD Veritor, Flowflex, and Celltrion DiaTrust.
  • Doctors across the country are seeing exposure to this toxic chemical.
  • Several poison centers throughout the United States have reported sodium azide exposures from the COVID-19 test kits. Goertemoeller estimated there have been 200-plus reported cases from the 55 poison centers nationwide. (Full article.)
  • If you suspect someone has been exposed, call the poison center at 800-222-1222.

I would like to point out the utter hypocrisy by comparing the SIX reports to the poison control center in the ivermectin deworming hoax, compared to the downplay of 200 reports due to COVID tests.

____________________

https://www.theepochtimes.com/fda-warns-of-possible-false-results-from-some-covid-19-tests

FDA Warns of Possible False Results From Some COVID-19 Tests

By Jack Phillips
March 2, 2022 Updated: March 2, 2022

The U.S. Food and Drug Administration (FDA) on Tuesday said that three rapid COVID-19 tests should not be used because of the potential for producing false results.

The FDA told people to stop using:

  • Celltrion DiaTrust COVID-19 Ag Rapid Test
  • SD Biosensor Inc. STANDARD Q COVID-19 Ag Home Test
  • Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing)

Summary:

  • all three tests are nasal swab tests
  • they are not authorized, cleared, or approved by the FDA
  • these tests have been recalled
  • Some poison control centers warned people not to improperly use at-home COVID-19 tests because they contain sodium azide, a potentially toxic substance. Some local poison control centers and hospitals have warned about an uptick in phone calls about exposures to the chemical.