We do not diagnose disease or recommend a treatment protocol or dietary supplement for the treatment of disease. You should share this information with your physician who can determine what nutrition and disease treatment regimen is best for you. Ask your physician any questions you have concerning your medical condition.

You can search this site or the web for topics of interest that I may have written (use Dr Simone and topic).

“We provide truthful information without emotion or influence from the medical establishment, pharmaceutical industry, national organizations, special interest groups or government agencies.” Charles B Simone, M.MS., M.D.

 

 

85% OF LIVES COULD HAVE BEEN SAVED IF EARLY INEXPENSIVE TREATMENT WITH HYDROXYCHLOROQUINE OR IVERMECTIN WERE USED

https://tinyurl.com/4637kyfy

 

Three major studies that were given as testimony in the U.S. Senate and the Texas State Senate showed that 85% of lives could have been saved if early inexpensive treatment with hydroxychloroquine or ivermectin were used.  

 

In 2005 the CDC published a paper entitled – “Chloroquine is a potent inhibitor of SARS coronavirus infection and spread.” Virol J. 2005 Aug 22;2:69.  

February 2020 – Some members of the Covid-19 Task Force want to use hydroxychloroquine (HCQ), a safe and effective FDA-approved drug, to control the rapidly spreading pandemic. The drug has been shown to prevent hospitalization if taken within the first five days of COVID-19 symptoms. HCQ costs about 60 cents per 200 mg tablet – treatment is one tablet twice a day for five days – $6.00  The FDA said HCQ is safer than Tylenol.

https://www.cnn.com/videos/politics/2020/04/22/hydroxychloroquine-trump-covid-19-study-mh-orig.cnn

June 29, 2020 – The Henry Ford COVID-19 Task Force in Detroit studied 2,541 patients (International Journal of Infectious Diseases) entitled, Treatment with Hydroxychloroquine, Azithromycin, and Combination in Patients Hospitalized with COVID-19.   https://www.ijidonline.com/action/showPdf?pii=S1201-9712%2820%2930534-8 (journal pre-proof). 

Conclusion: “Among hospitalized patients, use of hydroxychloroquine alone and in combination with azithromycin was associated with a significant reduction in-hospital mortality compared to not receiving hydroxychloroquine.”  

January 28, 2021 – FACEBOOK and AMERICAN JOURNAL OF MEDICINE admit their position on hydroxychloroquine was wrong.

 

 

Early use of hydroxychloroquine had a 79% lower mortality rate in countries that allowed the use of the safe drug.

A new study in the American Journal of Medicine in January showed a much lower mortality rate for patients with COVID-19 being treated with hydroxychloroquine while still at home. Also, the Facebook Oversight Board said it overturned its previous case on the effectiveness of HCQ.

HYDROXYCHLOROQUINE SAVES LIVES  https://bit.ly/38t2ZKl

IVERMECTIN SAVES LIVES  https://bit.ly/3aCNAtl  reviews many studies

Meta-analyses based on 18 randomized controlled treatment trials of ivermectin in COVID-19 have found large, statistically significant reductions in mortality, time to clinical recovery, and time to viral clearance.  In summary, based on the totality of the trials and epidemiologic evidence presented in this review along with the preliminary findings of the Unitaid/WHO meta-analysis of treatment RCTs and the guideline recommendation from the international BIRD conference, ivermectin should be globally and systematically deployed in the prevention and treatment of COVID-19.

WHO SUPPRESSED IVERMECTIN’s USE

1) MEDIA –

New York Times – “Senate hearing promoted unproven drugs and dubious claims about ivermectin.”

AP – “No evidence ivermectin is a miracle drug against COVID-19”

2) BIG TECH –

YouTube, owned by Google – banned ivermectin information from Dr Risinger and Dr. Martenson.

Twitter – blacklisted European Medical Journal for published study on ivermectin. 

Facebook – removed posts of Front Line Covid-19 Critical Care

3) NIH – formed a panel of doctors who decided what treatments can be given to patients. Ivermectin was not on the list and, in fact, the panel recommended use Remdesivir as highly recommended by Fauci – “diminishes the time to recovery.” Midway through the study, the endpoint was changed from mortality to recovery because Remdesivir does not save lives.  The World Health Organization does not recommend it at all.  Gilead owns Remdesivir.  Seven members of the panel are paid by Gilead, including the three co-chairs of the panel who choose the panel members.

 

 

 

2015 – During a National Academies of Science Workshop Peter Daszak said this, “until an infectious disease crisis is very real, present, and at an emergency threshold, it is often largely ignored.  To sustain the funding base beyond the crisis, a key driver is the media and the economics follow the hype.  Investors will respond if they see profit at the end of the process.”

 

 

Nov 9, 2015 – COVID-19 Birth Announcement in Nature Medicine.  The COVID-19 Bioweapon was created in plain sight.  This new intentionally made chimeric virus “shows a gain in pathogenesis“ (page 1512, middle of third paragraph).

Jan 9, 2017 – a few days before leaving office OBAMA RESUMED FUNDING for GAIN-OF-FUNCTION  

Jan 10, 2017 – the next day Fauci said “THERE WILL BE A SURPRISE OUTBREAK”

https://rumble.com/v1dgdhp-fauci-there-will-be-a-surprise-outbreak-january-10-2017.html

 

 

Jan 20, 2017 – Trump is inaugurated

 

2018 – The NIH infected 12 bats with a SARS-like coronavirus. The virus was shipped from Wuhan to an NIH lab in Montana (DailyMail https://dailymail.co.uk/health/article-12693441/fauci-nih-infected-bats-camp-david-coronavirus.html

 

September 18, 2019 – W.H.O. said by 2020 there would be an accidental or voluntary release of a respiratory pathogen and a global simulation so that we would accept a universal global vaccination.

October 18, 2019 –  – the global simulation – hosted by Gates Foundation in partnership with the World Economic Forum, and the Bloomberg School of Public Health Johns Hopkins.  Co-hosted by Avril Haines, former director of the CIA and today the Director of National Intelligence.

October 29, 2019 — 11 days later – Panel at the Michael Milken Institute Future of Medicine, discusses how to force and implement a new vaccine.

Listen especially to Rick Bright of BARDA (Biomedical Advanced Research and Development Authority of HHS) who said “a novel avian flu virus from China could allow them to push through a new universal flu vaccine much faster.”

https://youtu.be/sl_a-x09PQg

https://rumble.com/v18s8tv-october-29-2019-panel-discusses-how-to-force-and-implement-vaccine.html

November 17, 2019 – China records first known case of COVID-19 but US Senate Report states first death from COVID in China occurred in September 2019.

December 12, 2019 – NIH gives Ralph Baric the mRNA prototype to make the vaccine – this prototype was made weeks/months before Wuhan scientists had symptoms.  It is synthetic modified messenger RNA (mRNA) that is more stable, immunogenic, and potent. 

  

January 21, 2020 — CDC – first U.S. COVID Case

 

WE HAD A NATIONAL PANDEMIC RESPONSE PLAN FOR SUCH AN EMERGENCY that was initially tested in 2000, revised in 2005, and updated in 2017   https://www.hsdl.org/?abstract&did=438701

 

 

 

WHY WAS IT NOT FOLLOWED?

https://www.phe.gov/emergency/news/healthactions/phe/Pages/2019-nCoV.aspx

Under section 319 of the Public Health Service Act, the Secretary of Health and Human Services (HHS) may declare the existence of a public health emergency (PHE) such as a substantial outbreak of an infectious disease. Once a declaration is in place, the Secretary can take various actions, including making grants and contracts and waiving or modifying certain requirements of Medicare, Medicaid, the Children’s Health Insurance Program, and the Health Insurance Portability and Accountability Act.

 

HHS issued four section 564 declarations, allowing the FDA to issue EUAs for in vitro diagnostics, personal respiratory protective devices, other medical devices, and drugs and biologic products (including vaccines). A medical product can be made available under an EUA under four conditions: if the agent referred to in the declaration can cause a serious or life-threatening disease or condition; if there is no adequate, approved, and available alternative; if the product may be effective; and if the known and potential benefits of use of the product outweigh the known and potential risks. https://www.fda.gov/emergency-preparedness-and-response/mcm-legal-regulatory-and-policy-framework/mcm-emergency-use-authorities

Of the 372 total published papers showing that chloroquine / hydroxychloroquine is effective against SARS coronavirus, 22 were published during February and March 2020 and scores and scores more were published during 2020.

https://c19hcq.org/ – This Site provides a complete list of the published peer-reviewed papers.

 

FTX, a Bahamas-based cryptocurrency exchange and a partner with the World Economic Forum, filed bankruptcy November 2022, CEO Sam Bankman-Fried.  FTX also funded and disseminated information via TogetherTrials.com that hydroxychloroquine and ivermectin were not effective. The TogetherTrials were given Trial of the Year Award from the Society for Clinical Trials in San Diego (May 16, 2022).

 

 

May 22, 2020 – A Lancet article was RETRACTED but stated: Hydroxychloroquine or chloroquine decreased in-hospital survival and an increased frequency of ventricular arrhythmias when used for treatment of COVID-19.  

Hydroxychloroquine or chloroquine with or without a macrolide for treatment of COVID-19: a multinational registry analysis.  https://doi.org/10.1016/S0140-6736(20)31180-6

 

This intentional sabotage of the validated National Pandemic Response Plan paved the way for the “vaccine.”

 

Despite the long list of known possible adverse events, the FDA grants EUA to both Pfizer and Moderna 

 

December 11, 2020 – FDA granted an EUA for the Pfizer–BioNTech COVID‑19 vaccine.

December 18, 2020 – FDA granted an EUA to Moderna (mRNA-1273) 

 

 

The CDC had to change its definition of a vaccine on November 4, 2021 to justify its needs. 

Original definition: “A product that stimulates a person’s immune system to produce immunity to a specific disease, protecting the person from that disease.”

NOW, “A preparation that is used to stimulate the body’s immune response against diseases.”

 

 

Next came an invalid Emergency Use Authorization (EUA) for the “vaccine” – an EUA should only be granted if there was a “novel” or new feature to the virus that presents as a new threat that can be isolated, identified, evidenced, and supported by clear data.

 

1) the virus was not novel because there were 73 patents on parts of this virus and scores of medical papers, and

2) there were effective treatments

 

Also, Obama removed SARS from the Biological Select Agents and Toxins List (BSAT) because SARS – Coronavirus – no longer posed a threat to humans.

 

 

The following is an important summary of the harm of the “vaccines”

https://x.com/DrSimone/status/1722338317818024223?s=20

THE COVID “VACCINE” WAS NOT EFFECTIVE AND WAS NOT SAFE. AND IT DID NOT SAVE MILLIONS OF LIVES.  https://x.com/DrSimone/status/1722290948846109158?s=20…

This information has been taken with permission from

COVID-19 BIOWEAPON² PART 1 Executive Summary     https://bit.ly/3Fuiwdu

  Written: March 2020

     BIOWEAPON 1 – virus          

     BIOWEAPON 2 – shots

COVID-19 BIOWEAPON² PART 2  https://bit.ly/3eI11bK

COVID-19 BIOWEAPON² PREREQUISITE FOR U.S. INVASION – LONG TERM PLANNING 

https://tinyurl.com/37fbrevd

COUNTERMEASURE “VACCINE” – NOT EFFECTIVE, NOT SAFE, NOT MADE AT “WARP SPEED”

https://tinyurl.com/5n7tajc5

CHILDREN SHOULD NOT GET THE “VACCINE”

“ABOVE ALL DO NO HARM”

Written November 21, 2021  https://bit.ly/3nB4CyK

 

PROTECT YOURSELF FROM THE SPIKE: COVID-19 INFECTION and/or VACCINE – OUR NEXT HEALTH CRISIS

Written August 23, 2021  https://bit.ly/3kkrejY

 

HYDROXYCHLOROQUINE SAVES LIVES

© 2023 C B Simone, M.MS., M.D.