Archive for the ‘Treatment’ Category

Mainstream Media/Medicine Shouts About ‘Bungled Ivermectin Story’ While Ignoring Large, Prospective, Observational Study, Among Others

Recently, Medpage Today made sure to feature an article on how Reuters faced backlash after publishing an article stating that ivermectin was “effective” against Omicron in phase III trials, when what really happened was a Japanese company issued a press release stating ivermectin showed an “antiviral effect” against Omicron and other variants in joint non-clinical research.

The article further pigeon-holes ivermectin by calling it an “anti-parasitic drug” when research HAS shown it’s potent anti-viral effects by blocking importin, thereby preventing nuclear import and inhibiting viral access to cell nuclei. Many drugs currently on the market have multiple modes of action. Ivermectin is one such drug. It is both antiparasitic and antiviral.

The complete truth just isn’t convenient as an effective treatment would nullify COVID gene therapy injections.

They then bemoan that Twitter users state the uncorrected version will live-on on COVID conspiracy sites, as if Twitter is the fount of all knowledge.

The information that didn’t make the article is the fact that a city-wide, prospective, observational study of over 200,000 subjects found ivermectin substantially lowered infection, hospitalization, and mortality rates. 

Results:

The regular use of ivermectin led to:

  • a 68% reduction in COVID-19 mortality (25 [0.8%] versus 79 [2.6%] among ivermectin non-users; RR, 0.32; 95% CI, 0.20-0.49; p < 0.0001)
  • a 70% reduction in mortality when adjusted for residual variables (RR, 0.30; 95% CI, 0.19-0.46; p < 0.0001)
  • a 56% reduction in hospitalization rate (44 versus 99 hospitalizations among ivermectin users and non-users, respectively; RR, 0.44; 95% CI, 0.31-0.63; p < 0.0001)
  • a 67% reduction in hospitalization rate when adjusted for residual variables (RR, 0.33; 95% CI, 023-0.66; p < 0.0001)

While this study focused on prophylaxis, it’s important to note ivermectin’s obvious anti-viral qualities, which is the important take away. Proponents of ivermectin and HCQ have been quite clear that the earlier the treatment is initiated, the better the outcome (similarly to Lyme/MSIDS). This well written article called the Spartacus Letter explains:

  • the pathophysiology of COVID
  • the vast majority of COVID-19 cases are mild and do not cause significant disease
  • ventilation is killing patients
  • correct treatment for severe COVID-19 related sepsis is non-invasive ventilation, steroids, and antioxidant infusions
    • N-acetylcysteine, melatonin, fluvoxamine, budesonide, famotidine, cimetidine, and ranitidine are all antioxidants

But the most important information contained in the Spartacus Letter is the following:

Because of the way they are constructed, Randomized Control Trials will never show any benefit for any antiviral against COVID-19. Not Remdesivir, not Kaletra, not HCQ, and not Ivermectin. The reason for this is simple; for the patients that they have recruited for these studies, such as Oxford’s ludicrous RECOVERY study, the intervention is too late to have any positive effect.

So there you have it. RCTs will NEVER show benefit for ANY antiviral due to the way the studies are constructed.
Corrupt public health agencies know this.  They are banking on it.

To make their narrative work, they must ignore research that isn’t a RCT, like the aforementioned and numerous others:  https://ivmmeta.com/

Regarding ivermectin:

Evidence base used for other COVID-19 approvals
Medication Studies Patients Improvement
Molnupiravir (UK) 1 775 50%
Budesonide (UK) 1 1,779 17%
Remdesivir (USA EUA) 1 1,063 31%
Casirivimab/i.. (USA EUA) 1 799 66%
Ivermectin evidence 78 85,743 64% [57‑70%]

As is clearly seen from the table, the evidence for ivermectin utilizes 78 studies and nearly 86,000 people vs. only ONE study and a fraction of the patients for drugs receiving emergency use authorization (EUA).  It is also clear that ivermectin gives greatest improvement over those pushed by mainstream medicine and corrupt public health ‘authorities’.

Please see this excellent video on the powerful players colluding together to suppress ivermectin, as well as a revealing transcript of a conversation with Dr. Andrew Hill, who admitted to caving to pressure to downplay the benefits of ivermectin as a COVID treatment.

The clinical studies that do exist, and the consilience of the real-world data (RWD), show that early use of ivermectin reduces mortality by somewhere between 50 and 85%. ~ Dr. James Lyons Weiler

As the World Tribune reports:

In a recent Zoom call, Dr. Pierre Kory of the Front Line COVID-19 Critical Care Alliance outlined numerous details showing the World Health Organization (WHO) knowingly suppressed data on the effectiveness of ivermectin against the virus in order to benefit the vaccine interests of Big Pharma.

“It’s criminal,” Kory said. “It’s literally criminal.” The drug “could have saved half a million lives this year if it had been approved.”

The WHO, Kory contends, is simply taking part in the tactics of a time-worn “Disinformation Playbook.” The term was coined by the Union of Concerned Scientists 50 years ago to describe the strategies corporations have developed over decades to “attack science when it goes against their financial interests.”

According to the Tribune, this disinformation strategy has five parts:

  1. The Fake – Conduct counterfeit science and try to pass it off as legitimate research.  Please see this excellent article showing 5 studies where researchers present conclusions that don’t match the data.
  2. The Blitz – Harass scientists who speak out with results reviews inconvenient for industry.
  3. The Diversion – Manufacture uncertainty about science where little or none exists.
  4. The Screen – Buy credibility through alliances with academia or professional societies.
  5. The Fix – Manipulate government officials or processes to influence policy inappropriately.

Medpage Today misses the point entirely and is only serving as a Big Pharma shill to the demise of sick patients.  It is actively taking part in the disinformation strategy outlined above. 

Promising Lyme Antibiotics in Development

https://www.treatlyme.net/guide/hygromycin-a-and-azlocillin-for-lyme-disease  Video Here (Approx 2 min)

Promising Lyme Antibiotics in Development

There are two recent antibiotic discoveries that could change the course of Lyme disease treatment. One of these is Azlocillin and the other is Hygromycin A.

  • Azlocillin is an FDA approved antibiotic shown in laboratory experiments, including mouse experiments, to effectively treat persister phase and growth phase Lyme. You can read more about persisters in [11] Lyme Infection. There is one hitch—no pharmaceutical company currently produces this medication. This may change in the next couple of years as a company called FlightPath is working to bring this to market. While mouse experiments and other science experiments look promising, we will have to see what human studies eventually show.
  • Hygromycin A is a substance found in soil that targets Lyme spirochetes and does not appear to target other bacteria—so it should not disturb the intestinal microbiome. No experiments to date have been published that determine if it will also treat persister phase Lyme. FlighPath is also developing this novel therapeutic. However, because it is not US Food and Drug Administration (FDA) approved, it could take eight years or more to bring this to market. FlightPath must first perform the required laboratory and clinical studies to get FDA approval.

Lyme Protocol

For current treatment options that may speed your Lyme recovery see The Ross Lyme Support Protocol

Watch Dr. Marty Ross go through the antibiotics in the top link.

Also see Dr. Ross’s Lyme disease herbal and RX antibiotic Guide UPDATE:  https://www.treatlyme.net/guide/lyme-disease-antibiotic-guide

For more:

Level of Evidence & WaPo’s Claims of Ivermectin Toxicity & “Over 500,000 Deaths Could Have Been Prevented”

https://popularrationalism.substack.com/p/level-of-evidence-and-washington?

Level of Evidence and Washington Post’s Claims of Ivermectin Toxicity

A letter to the editor of NEJM is cited as providing evidence of a host of toxic side effects… but in tracking down the reference, the evidence falls far short of “toxic” and “causal”.

The Washington Post’s article, “Online archives where scientists post their research spark information revolution” writes about a non-peer-reviewed study on Ivermectin was “retracted” by a pre-print server (technically, an impossible feat given that preprint servers do not technically “publish” studies, because the works are not peer-reviewed).

They also throw in this sentence:

“not to mention contributed to a host of serious side effects among those who ingested ivermectin with no proven benefit against covid-19.”

That reads as if the study found a host of serious side effects, but the WashPo article linked to a letter to the editor of the New England Journal of Medicine.

Was this letter a peer-reviewed study that demonstrated causality of the alleged side effects WashPo claims the study has “contributed to”?

No. It was not. The letter merely described 21 reported sets of symptoms following Ivermectin use based on phone calls to a poison control center:

“Of the 21 persons who called in August, 11 were men, and most were older than 60 years of age (median age, 64; range, 20 to 81). Approximately half (11 persons) were reported to have used ivermectin to prevent Covid-19, and the remaining persons had been using the drug to treat Covid-19 symptoms. Three persons had received prescriptions from physicians or veterinarians, and 17 had purchased veterinary formulations; the source of ivermectin for the remaining person was not confirmed. Symptoms had developed in most persons within 2 hours after a large, single, first-time dose. In 6 persons, symptoms had developed gradually after several days to weeks of repeated doses taken every other day or twice weekly. One person had also been taking vitamin D to treat or prevent Covid-19. Reported doses ingested by the persons who had been using veterinary products ranged from 6.8 mg to 125 mg of 1.87% paste and 20 to 50 mg of the 1% solution. The dose of the human-use tablets was 21 mg per dose twice weekly for prevention.

Six of the 21 persons were hospitalized for toxic effects from ivermectin use; all 6 reported preventive use, including the 3 who had obtained the drug by prescription. Four received care in an intensive care unit, and none died. Symptoms were gastrointestinal distress in 4 persons, confusion in 3, ataxia and weakness in 2, hypotension in 2, and seizures in 1. Of the persons who were not admitted to a hospital, most had gastrointestinal distress, dizziness, confusion, vision symptoms, or rash.

These cases illustrate the potential toxic effects of ivermectin..”

The question for the WashPo article author, and WashPo, is how is this “a host of serious side effects” when

(1) Frequency data are not available (we don’t know how many people were using Ivermectin. Is 21 a lot? A little? 1 in 1,000? 1 in 1,000,000?

(2) Causality has not been determined (calls from poison control are not clinical study-level evidence). GI issues, ataxia and hypotension also happen in people taking any number of over-the-counter drugs, prescription drugs and vaccines.

(3) None of these events are considered “serious” (Seizures following vaccination are not considered “serious”).

Imagine if Ivermectin were a vaccine… and 21 phone calls later, the reported outcomes were reported as “caused by” and “serious”.

It seems that the level of evidence need to bury an inexpensive treatment is far, far less than needed to determine causality of vaccine injury.

With this type of loose “reporting”, the legacy press loses yet another point on the credibility scale.

Make that four points (-4).

Actually, make it five: WashPo fails to report the 77 other studies on Ivermectin.

This is why people who read the news need to check the references and see for themselves whether their news source is accurately representing what’s going on.

And it’s time we start holding such “news” outlets accountable for their abuse of the public trust and of scientific evidence.

_________________

https://thehighwire.com/videos/over-500000-covid-deaths-could-have-been-prevented/

“OVER 500,000 COVID DEATHS COULD HAVE BEEN PREVENTED”

On the heels of the groundbreaking ‘Covid-19: Second Opinion” panel, Dr. Richard Urso joins Del in-studio to talk through some of the most eye-opening statements from the over 5 hour long hearing featuring the greatest minds in science and health.

Dr. Urso corrects Senator Johnson who stated that there weren’t any treatments at the beginning of the ‘pandemic.’ Urso states there were effective treatments that worked from the very get-go. He used a combination of HCQ, azithromcin, vitamin D, aspirin, and steroids way back in March.

Urso also states the denial of natural immunity needs to STOP, and that he has never called the FDA, NIH, or the CDC ONE time for advice.  Those organizations are not involved in medical education. Their dictating medical practices also needs to stop. The current regime needs to be completely reinvented because it is corporate practice of medicine telling doctors what to do when they already know what to do.

Go here for a four-part talk by Dr. Urso covering everything from COVID testing, deaths, lockdowns, to effective treatments.

Also, go here for “The Indefensible Approval of Pfizer and Merck Drugs Compared to the Snubbing of Ivermectin.”

It is quite clear there are two standards. The ‘powers that be’ can do no wrong and can say anything they want even if it’s completely untrue, illogical, and unscientific.

#SecondOpinion #RonJohnson #DrRichardUrso

For more:

Exponential Clinical Outcomes 2021 Notes

https://www.betterhealthguy.com/eco2021

ECO 2021 Live

I had the opportunity to attend ECO 2021 held online on October 28-30, 2021.   ECO stands for Exponential Clinical Outcomes.  This is one of the most forward-thinking events I have attended.

The event is the brainchild of Dr. Todd Watts and Dr. Jay Davidson who also created CellCore Biosciences and Microbe Formulas.  I’m grateful for their products, and I take several of them daily.

CellCore Biosciences is their practitioner line while Microbe Formulas is their consumer line. While many of the products are available from both companies, there are some differences in some products in terms of formulation or availability in the Microbe Formulas product line.

Disclaimer: Nothing in this text is intended to serve as medical advice. All medical decisions should be made only with the guidance of your own personal licensed medical authority.

Disclaimer: This information was taken as notes during the training course and may not represent the exact statements of the speakers. Errors and/or omissions may be present.

Note: As this information may be updated as any errors are found, I kindly request that you link to this single source of information rather than copying the content below. If any updates or corrections are made, this will help to ensure that anyone reading this is getting the most current and accurate information available. ~ The Better Health Guy

Topics covered:

  • Glyphosate toxicity
  • The protocol approach
  • Mastering Mitochondria
  • The Krebs Cycle
  • Optimizing Mitochondrial function
  • Is your Water keeping you sick?
  • Solutions for the Parasite Epidemic
  • #1 Stealth Infection you are missing
  • The Gut, The Brain, and Autism
  • The Wrecking Ball of Estrogen Dominance
  • Chemicals and Biotoxins in Dentistry
  • Case studies: Skin Changes
  • Thoughts on Vitamin D
  • Importance of Emotional Clearing to Detox
  • Mental and Emotional Case Studies

For more:

FDA Halts Use of Most Monoclonal Antibodies for COVID Treatment

https://www.medpagetoday.com/infectiousdisease/covid19/96838?xid=nl_covidupdate_2022-01

FDA Halts Use of Most Monoclonal Antibodies for COVID Treatment

— Bamlanivimab/etesevimab, REGEN-COV not expected to work against Omicron
Last Updated January 25, 2022
A computer rendering of a monoclonal antibody cocktail binding to a Covid virus

The monoclonal antibody combinations bamlanivimab/etesevimab and casirivimab/imdevimab (REGEN-COV) should only be used for COVID-19 patients exposed to variants other than Omicron, the FDA said on Monday.

The agency revised the emergency use authorization (EUA) for the two antibody cocktails for use “only when the patient is likely to have been infected with or exposed to a variant that is susceptible to these treatments,” Patrizia Cavazzoni, MD, director of the FDA’s Center for Drug Evaluation and Research, said in the statement. (See link for article)

____________________

SUMMARY:

  • FDA cited “markedly reduced activity against the Omicron variant” as the reason for this revision.
  • CDC data indicate that over 99% of U.S. COVID cases are from Omicron.
  • The FDA action avoids exposing patients to side effects such as injection site reactions or allergic reactions. It is ironic the FDA isn’t concerned at all about COVID injection side-effects and deaths.

The FDA used the results of laboratory experiments in its sudden and unexpected decision to revoke EUAs for certain monoclonal antibody treatments for COVID-19, stating that data showed the treatments were ineffective against the Omicron variant.  

The FDA; however, has been accused of being inconsistent with EUA COVID treatments since they authorized Merck’s antiviral pill in spite of clinical data demonstrating disappointing results. Remdesivir also has been conditionally recommended against use by the WHO due to lack of efficacy yet remains authorized by the FDA. The COVID injections also have far less efficacy against Omicron yet are still being used.

Similarly to the COVID injections wanning for variants, now one of mainstream medicine’s preferred COVID treatments also doesn’t work. Dr. Ruby explains that in her practice those getting COVID again are those who have either been treated with monoclonal antibodies or have gotten the COVID injections.  She also states that getting the antibodies is like renting an army for the day.  That they come in, provoke the immune system to fight, and then quickly disappear – unlike natural immunity which continues to work on your behalf. This treatment is also experimental, and much remains unknown.

Another important issue to point out is that PCR testing can not distinguish what variant you have.

Meanwhile, the censorship on doctors and effective COVID treatments continues under our corrupt public health ‘authorities’ who own patents on the pathogen, the tests, the treatments, and the “vaccines.”  Hospitals have become modern-day “killing fields,” only utilizing the ineffective and dangerous treatments approved by corrupt authorities who care more about governmental incentive money than they do about patients.

    • Fauci made the unusual move of announcing at a press conference from the White House in April, 2020 that the anti-viral Remdesivir for COVID diminishes time to recovery. He doesn’t discuss mortality at all. 
    • NIAID (where Fauci works) actually paid for the NIH study he alludes to.  Being fully aware of the study he also knew that midway through it the primary end-point was changed from mortality to time to recovery. This was obviously done because researchers saw that remdesivir had no significant impact on mortality. Changing endpoints midway in a study should raise a lot of red-flags.
    • Meanwhile, using evidence based on much larger studies, the WHO did not recommend remdesivir as they stated that there is no evidence that it improves survival or any other metric in patients.
    • ‘Slight of hand’ statistical trickery such as:
    • changing study end points
    • using non-infection efficacy numbers
    • and omitting absolute risk are continually being used to mislead the public into believing the accepted narrative that HCQ and Ivermectin are ineffective and/or dangerous, but that the COVID-19 injections are safe and effective.
    • Remdesivir is manufactured by Gilead Sciences, a California-based company which has been accused of bioterrorism.
    • The video then explains how at least 7 members of the COVID-19 treatment panel have financial ties to Gilead Sciences.
    • The three co-chairs who select the other panel members do not disclose financial ties to Gilead, but two of the chairs both receive financial support from Gilead. The third co-chair was one of the authors of the NIAID funded remdesivir study.  His name is not listed as a study author, you have to dig for it by looking at the financial disclosure form of conflicts of interest.
    • These conflict-riddled panelists push the drug they make money from but know full well it has no effect on COVID-19 survival. This is professional negligence of the worst sort that has potentially resulted in millions of deaths globally.
    • They choose to suppress ivermectin with study after study proving its effectiveness on mortality, and push their own ineffective drug.
    • Similarly to how Sweden has acted as a placebo arm in this vast evil experiment by refusing to lock down and force masks, resulting in ZERO COVID deaths, the state of Uttar Pradesh, India, which has about 70% of the U.S. population, chose to authorize ivermectin for those testing positive, for their primary contacts and for health care workers. Ivermectin brought COVID deaths down to ZERO.
    • Ivermectin could have ended the pandemic LAST SUMMER.
    • The suppression and censorship of Ivermectin and other treatments is a crime.
Spread the word.  Effective treatments are purposely being withheld from the public causing needless deaths.