Month: November 2023

QUOTE:

The Covid-19 coronavirus was “intentionally released” by the United States in Wuhan, China, with the target to trigger a global pandemic to raise public acceptance of vaccines, a US businessman specializing in patent auditing said.

David Martin, the founding chairman of M Cam asset management company, said at an International Covid Summit organized by the European Parliament in Brussels earlier this month that the US was responsible for the making of both coronaviruses causing the outbreaks of severe acute respiratory syndrome – or SARS – in 2003 and the Covid-19 pandemic in the past three years. https://www.thestandard.com.hk/section-news/section/11/252653/US-‘intentionally-released-Covid-virus-in-Wuhan’-EU-summit-told

QUOTE: One man’s family took his care into their own hands when he was hospitalized with COVID-19. As a result, they believe they may have saved his life.

Shannon Fletcher, daughter of David Dentz, spoke with Liz Collin this week to share her dad’s story and long battle with COVID.

Dentz was hospitalized with COVID-19 for 208 days, one of the longest COVID stays in the state. Not until his family began slipping him ivermectin did his health begin to look up, Fletcher said.

Methodist Hospital’s protocols required doctors to not administer ivermectin, Fletcher said. Two weeks into Dentz’s hospital stay, Fletcher and her family were paying out of pocket for an advocate and an attorney, trying to get Dentz help the hospital would not provide.

They were not allowed to visit him during this time, and the family held a “Save Dave” protest outside of the facility. Fletcher believes her father, who was not vaccinated, received worse treatment than those who were vaccinated against COVID.

The hospital “shamed” the family when they didn’t want to give up on Dentz’s life, Fletcher said. Finally, Fletcher decided she wanted to bring ivermectin to her father and slip some in his mouth.

“There’s nothing that they’re going to do, and [they’re] already telling me he’s going to die, so we might as well try it,” Fletcher said.

After she succeeded once with the plan, her family continued sneaking ivermectin paste into Dentz’s mouth over the next five days.

“[The amount] was based on weight, so we took a small amount — and I know the media is going to put it down and call people crazy and this and that — but I don’t care because I believe he’s here for that reason,” Fletcher said.

“The day after we gave him ivermectin, Angie got a call and the doctor said she could not believe the progress that he was making. The very next day.”

Then Dentz was transferred out of the hospital to a specialist who said he was “overmedicated” and “over sedated,” according to Fletcher.

Over 200 days from his first admittance, Dentz was discharged. Fletcher said he struggles to breathe and has stage 3 kidney failure due to the remdesivir.
“Considering where we were, he’s doing amazing,” she said.

https://alphanews.org/family-says-they-saved-dads-life-by-sneaking-him-ivermectin-during-200-day-hospitalization/

QUOTE: A federal appeals court allowed three doctors to sue the FDA over a series of website and social media posts condemning ivermectin as a treatment for COVID-19. The doctors alleged the FDA exceeded its authority by offering medical advice and “that FDA’s messaging interfered with their own individual medical practice.”

The lawsuit stems from a series of FDA posts advising consumers not to take horse ivermectin but failing to acknowledge the existence of a human ivermectin formulation, including one tweet advising consumers, “Hold your horses, y’all”:

The trial court dismissed the doctors’ lawsuit after finding sovereign immunity barred their three claims. The appeals court reversed on one claim, finding plausible the argument the FDA exceeded its statutory authority by offering medical advice instead of medical information.

The firm Boyden Gray, which represents the doctors, issued a press release praising the decision: In a matter critical to stopping federal overreach into the practice of medicine, Boyden Gray PLLC welcomes a decision from the U.S. Court of Appeals for the Fifth Circuit . . . rejecting the government’s blanket assertion of sovereign immunity and allowing the case to proceed.

Dr. Robert Apter alleges he was twice referred to state medical boards for prescribing ivermectin off-label, with the referrals citing the FDA’s posts.

Dr. Apter and Dr. Mary Bowden allege pharmacies refused to fill their ivermectin prescriptions because of the FDA’s posts. Dr. Bowden claims she lost admitting privileges at a hospital after tweeting about using ivermectin to treat COVID-19.

Dr. Paul Marik, co-leader of FLCCC, alleges he lost positions at a medical school and hospital “for promoting the use of ivermectin.”

https://legalinsurrection.com/2023/09/appeals-court-doctors-can-sue-fda-for-condemning-ivermectin-as-a-covid-19-treatment-resulting-reputational-harm/

The Biden administration will deliver another round of free at-home COVID-19 tests nationwide through its COVIDTests dot gov website, a spokesperson for the U.S. Department of Health and Human Services (HHS) said.

The site, one of the few places where free rapid COVID tests are still available for Americans after the end of the pandemic emergency in May, resumed its operations last September ahead of the winter months and a potential spike in infections.

For those who have already ordered four free at-home rapid tests through the site, an additional four tests will be available per household at no cost. Otherwise, anyone who has yet to place orders this fall can order eight tests per household.

Since September, about 14.5M households have ordered a total of 58M tests, the Administration for Strategic Preparedness and Response (ASPR), a unit within HHS, said.

“We’re going to see families gather with older loved ones and younger loved ones and it’s important that they are able to protect their loved ones from COVID as we head into the winter months,” head of ASPR Dawn O’Connell noted.

According to latest CDC data, as of Nov. 11, weekly COVID hospitalizations in the U.S. have exceeded 16K with ~9% rise from 15K a week ago.

Republican voters in Southwest Arkansas’ District 3, which stretches from Bismarck to the Louisiana line, including the cities of Arkadelphia, Gurdon, Hope, Prescott, and Magnolia, could have no better choice for State Senator than Mark Silvey of Nevada County. Mark Silvey might not be a name you recognize from politics, and we think that’s a good thing. He is a pastor, a small business owner, and a citizen who realizes it’s time for regular folks to get off the sidelines and become involved in government. Silvey stands strongly against mandates of any kind; he is for complete abolition of abortion; he will fight against libraries that provide pornography to minors; and he believes state government should be fiscally responsible, accountable to the taxpayers, and transparent. Silvey believes in educational freedom; he reminds that children belong to the parents, not the state. The bottom line – Mark is the real deal; you’ll never have to spend any time asking him to vote correctly, because he will be a true one hundred percent patriot senator. Our entire state will be blessed with this freedom-fighter in the state senate. Please join us in supporting Mark Silvey for State Senate, and consider a donation to his campaign: https://www.silveyforsenate.com/

Defendant the Republic (DTR) has just obtained another set of documents from the Food and Drug Administration (FDA) relating to the agency’s approval of Moderna’s COVID-19 vaccine “Spikevax.” DTR received these Moderna files as a result of its ongoing Freedom of Information Act (FOIA) lawsuit against the FDA. They are available for download below.

The new records include a listing of adverse events for thousands of clinical participants who received doses of Moderna’s COVID-19 vaccine. The adverse events, many of which started mere days after vaccination, include: elevated blood pressure, swollen lymph nodes, high fevers and fatigue, rashes, and vertigo.

These are just some of the adverse reactions that clinical trial participants had to Moderna’s COVID-19 vaccine. In July of 2023, DTR released the initial set of Moderna documents – the first significant release of data from Moderna’s COVID-19 clinical trials – which revealed serious adverse events following the company’s vaccine, including death and neurological disorders.

Also released are: summaries of the duration of days that passed from the date of injection (for both the first and second shots) and the onset of adverse reactions; Moderna responses to FDA comments concerning vaccine effectiveness; and other FDA comments to Moderna concerning the clinical results.

Before the end of the year, DTR anticipates the FDA, in compliance with its FOIA obligations, will produce thousands more pages of Moderna records. We will summarize and release those records to the public once available.

Defendant the Republic (DTR) has just obtained another set of documents from the Food and Drug Administration (FDA) relating to the agency’s approval of Moderna’s COVID-19 vaccine “Spikevax.” DTR received these Moderna files as a result of its ongoing Freedom of Information Act (FOIA) lawsuit against the FDA. They are available for download below.

The new records include a listing of adverse events for thousands of clinical participants who received doses of Moderna’s COVID-19 vaccine. The adverse events, many of which started mere days after vaccination, include: elevated blood pressure, swollen lymph nodes, high fevers and fatigue, rashes, and vertigo.

These are just some of the adverse reactions that clinical trial participants had to Moderna’s COVID-19 vaccine. In July of 2023, DTR released the initial set of Moderna documents – the first significant release of data from Moderna’s COVID-19 clinical trials – which revealed serious adverse events following the company’s vaccine, including death and neurological disorders.

Also released are: summaries of the duration of days that passed from the date of injection (for both the first and second shots) and the onset of adverse reactions; Moderna responses to FDA comments concerning vaccine effectiveness; and other FDA comments to Moderna concerning the clinical results.

Before the end of the year, DTR anticipates the FDA, in compliance with its FOIA obligations, will produce thousands more pages of Moderna records. We will summarize and release those records to the public once available.

https://substack.com/redirect/278eca80-80ca-4b81-9a3e-5eac17e07628?j=eyJ1IjoiMmUxY2FsIn0.aGROOmEuAH_toaDS2kmmHKY2uItOgHjCq2qfbI9HWXs