Archive for the ‘Viruses’ Category

Dr. Fauci Pushes For COVID-19 Vaccine Despite Research Showing Vaccinated May Get Sicker And Even Die (Lab Animals Got Sicker Too)

Approx. 5 Min

Dr. Fauci & COVID-19: Therapeutics Now OR Vaccines Later?

There is a raging debate in our government. How should America respond to the Coronavirus crisis? With therapeutic drugs? Or with a vaccine? Dr. Anthony Fauci is predictably shining a spotlight on risky and uncertain coronavirus vaccines that may not be available for two years, rather than prioritizing the short-term therapies that patients need right now.

In light of the immunity from liability guaranteed by the PREP Act during declared emergencies, fast-tracked vaccines are a sweetheart deal for both biopharma and government. Will Big Pharma and biotech companies be allowed to cash in on this catastrophe with speculative, patentable vaccines at the expense of the therapeutics needed to save lives now?

To keep updated on this issue and others, sign up for our free emails: ChildrensHealthDefense.org

___________________

**Comment**

To this day the U.S. does NOT have an effective COVID-19 test, which means the media is reporting numbers that are completely unreliable.  Then there’s the issue of effective treatments that the CDC would rather push aside to focus on “sexy” vaccines that will make them money.  https://madisonarealymesupportgroup.com/2020/03/21/study-shows-covid-19-testing-as-bad-as-lyme-msids-testing/

None of this this new and has been going on for a long time.

Fauci quietly sits on the Leadership Council of the Bill & Melinda Gates Foundation’s Global Vaccine Action Plan, which is currently reaching the finality of its so-called “Decade of Vaccines” initiative that began in 2010. This fully explains why he’s gone all-in for a future Wuhan coronavirus (COVID-19) vaccine, and why he’s signaled that Americans will continue to be held hostage until they agree to get it.  https://www.sgtreport.com/2020/04/anthony-fauci-wants-coronavirus-vaccines-to-be-forced-on-all-americans/

CDC/HHS is a captured agency and not to be trusted with anything:  https://madisonarealymesupportgroup.com/2016/11/29/spider-attacks-cdc/

https://madisonarealymesupportgroup.com/2018/04/06/cdcs-troubling-lack-of-research-ethics/

https://madisonarealymesupportgroup.com/2017/01/13/lyme-science-owned-by-good-ol-boys/

https://madisonarealymesupportgroup.com/2018/07/18/hhs-not-to-be-trusted-with-lyme/

https://madisonarealymesupportgroup.com/2019/02/16/the-cdc-is-a-captured-agency/

For more:  https://madisonarealymesupportgroup.com/2020/03/28/epidemiologist-behind-highly-cited-coronavirus-model-drastically-downgrades-projection/

https://madisonarealymesupportgroup.com/2020/03/27/a-fiasco-in-the-making-as-the-coronavirus-pandemic-takes-hold-we-are-making-decisions-without-reliable-data/

Mouse study:  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3209347/A Double-Inactivated Severe Acute Respiratory Syndrome Coronavirus Vaccine Provides Incomplete Protection in Mice and Induces Increased Eosinophilic Proinflammatory Pulmonary Response upon Challenge

Epidemiologist Behind Highly-Cited Coronavirus Model Drastically Downgrades Projection

https://www.dailywire.com/news/epidemiologist-behind-highly-cited-coronavirus-model-admits-he-was-wrong-drastically-revises-model

Epidemiologist Behind Highly-Cited Coronavirus Model Drastically Downgrades Projection

By  Amanda PrestigiacomoDailyWire.com

Epidemiologist Neil Ferguson, who created the highly-cited Imperial College London coronavirus model, which has been cited by organizations like The New York Times and has been instrumental in governmental policy decision-making, offered a massively downgraded projection of the potential deathtoll on Wednesday. (See link for article)

___________________

**Comment**

A few key quotes:

Ferguson’s change of tune comes days after Oxford epidemiologist Sunetra Gupta criticized the professor’s model.

“I am surprised that there has been such unqualified acceptance of the Imperial model,” Gupta said, according to the Financial Times.

The important issue Gupta’s team raises is that COVID-19 was spreading much earlier than suspected and concludes that as many as half of the people in the United Kingdom have already been infected by COVID-19.

Which brings up the probability of this happening in the U.S. as well.

My entire family, as well as many neighbors and friends feel we’ve already had COVID-19 earlier this year and live to tell the tale.

For more:  https://blogs.mercola.com/sites/vitalvotes/archive/2020/03/26/stanford-professor-states-fatality-rates-at-least-10-fold-lower-than-estimates.aspx

Excerpt: 

But, like The Wall Street Journal’s writers point out, it is quite possible that “A universal quarantine may not be worth the costs it imposes on the economy, community and individual mental and physical health” and that statisticians should be called upon to “evaluate the empirical basis of the current lockdowns.”

https://madisonarealymesupportgroup.com/2020/03/21/study-shows-covid-19-testing-as-bad-as-lyme-msids-testing/

https://madisonarealymesupportgroup.com/2020/03/27/a-fiasco-in-the-making-as-the-coronavirus-pandemic-takes-hold-we-are-making-decisions-without-reliable-data/

And the most damning of all articles, Weiler points out that the CDC itself is behind the testing fiasco in the U.S. by insisting on having its own test so they could profit, create a vaccine, and own more patents at the expense of public health:  https://madisonarealymesupportgroup.com/2020/03/27/cdcs-deadly-testing-fiasco-centralization-of-public-health-authority-a-threat-to-national-security/

 

 

 

Cuomo Admits Decision to Quarantine Everyone At Once Was ‘Not The Best Strategy’

https://www.dailymail.co.uk/news/article-8156457/Cuomo-says-probably-not-best-strategy-quarantine-once.html

Cuomo admits his decision to quarantine everyone at once was ‘not the best strategy’ and that he is ‘working on’ release of coronavirus antibody test that will allow people to go back to work

(See link for article)

____________________

**Comment**

Dr. Birx Admits Initial Death Estimates Too Extreme

In a nutshell, she admits that the CDC STILL does not have an accurate test as well as the fact that the models used were faulty and don’t reveal what’s happening in reality (South Korea, Italy, Spain).

According to this: “must read” article,  https://madisonarealymesupportgroup.com/2020/03/27/cdcs-deadly-testing-fiasco-centralization-of-public-health-authority-a-threat-to-national-security/ perfectly good, reliable tests were offered to the U.S., but similarly with Lyme disease testing the CDC insists upon having their own.  As a result the U.S. has absolutely NO idea how many cases there are due to extremely faulty testing: https://madisonarealymesupportgroup.com/2020/03/21/study-shows-covid-19-testing-as-bad-as-lyme-msids-testing/

Excerpt:

Germany is not suffering from a raging infection outbreak because they have been conducting accurate testing since the onset of their first infection. The World Health Organization (WHO) offered the US CDC the test from Germany – and yet CDC made the deadly decision to develop their own test.

The German test was ready and available on January 17th 2020 – including published details of the protocol.

The test had also already been validated for specificity to SARS-2-CoV – using human samples – meaning it would not accidentally give false positives for other respiratory viruses – and also meaning that it would not give a false positive from human genes in the human samples.

Weiler, points out how the CDC has a history of insisting upon their own testing so they can corner the market, putting them in direct competition with the private sector.  He rightly points out what all of us in Lymeland have been screaming about:

It isn’t ethical to be in charge of public health AND own licenses to products.  

Agency scientists should not be allowed use US taxpayer’s funds to develop “their own” test. CDC, and HHS, in fact, should not own anything.”  James Lyons-Weiler

Those suffering with tick-borne illness have had to work about the faulty testing issue for over 40 years.  Doctors to this day are sending people home with a false sense of security after they test negative on the only approved CDC 2-tiered tests available. For decades the CDC has vilified small CLIA-approved labs doing more specialized testing for Lyme disease.  On their website a while back they actually had the nerve to call these tests “home-brewed,” always casting a negative light on ANY test other than their’s.  

I pray this COVID-19 testing fiasco shines a light on a very real problem – the CDC is a captured agency.

The Truth About Hydroxychloroquine (Plaquenil) in the Treatment of COVID-19

The truth about plaquenil

THE TRUTH ABOUT HYDROXYCHLOROQUINE (Plaquenil) IN THE TREATMENT OF COVID-19

By Dr. Alain Mass

Since the intervention of the President of the USA, Donald Trump announcing that the FDA approved Hydroxychloroquine in the treatment of COVID-19, the news spread that a treatment was now available. However, on the same day, the FDA denied having given the approval for this drug. We are now facing questions and requests from patients for this medication that medical professionals cannot give without going astray from the current standard of care established by the FDA. More concerning is the consequences on the epidemic and on lives to refrain the prescription of Hydroxychloroquine. Is Hydroxychloroqine really a treatment for COVID-19? Is there any alternative treatment? Is Hydroxychloroquine really dangerous to the point to limit or to delay its use until studies confirm the validity of its use in the treatment of COVID?

Didier Raoult, M.D. is a Professor in Infectious Diseases in Marseille, France. He is ranked as the first world expert in communicable diseases by the online resource, http://www.expertscape.com. He is the leader in France in the research on COVID-19. He is also an expert in Plaquenil since he has worked for the past 10 years on Plaquenil to treat other diseases. He is currently the European voice who promotes the use of Hydroxychloroquine against the position of the FDA. As a French native, I was able to follow the interviews that the Professor Didier Raoult gave and because lives may be saved today with the use of Hydroxychloroquine I feel an ethical duty to share the expert advice that supports the use of Hydroxychloroquine (Plaquenil).

Plaquenil has been used for the past 70 years as a drug to treat and to prevent malaria. Plaquenil’s safety has been proven, having been used by millions of people during this period. Its safety profile is well-known, which is not the case of newer drugs that may be safe in the early studies, but often turn out to be dangerous over time.

If, two months ago, you would have to go to Africa, Asia or any endemic zone of malaria the same doctor who, today, refuses to give you Plaquenil, based on the FDA instructions, would have given you Plaquenil for weeks or months without any hesitancy and probably even without looking up the potential side effects. Malaria may kill and the prevention of a potential lethal disease has justified for the past 70 years this practice that nobody never discussed. Suddenly, in 2020, Plaquenil became a dangerous drug when there is a threat of crisis in Plaquenil supply. Is Malaria much worse than COVID-19? Is the risk of being bitten by a mosquito in a hotel much higher than catching COVID-19 in your local supermarket full of sick individuals or by touching door knobs where the virus can stay 9 days?

Three studies have been published recently by Chinese doctors showing the efficacy of Plaquenil on COVID-19. One study reported by the Pr. Didier Raoult, showed the eradication of coronavirus in 75% of patients with hydroxychloroquine alone and when combined with Azithromycin an eradication in 95% of cases. Pr. Raoult published a few days ago his own study showing similar results. Pr. Raoult thinks that Chinese doctors are reliable. They were the first to face this epidemic, have the largest experience in COVID-19 patients and have already published more than 20 studies. 

The usual rule in Medicine requires protocols, well conducted double-blind randomized studies, studies at large scale to officially promote a medication. Dr. Hahn, director of the FDA states:

“We must ensure these products are effective: otherwise we risk treating patients with a product that might not work when they could have pursued other more appropriate treatments”.

The problem is that we do not have yet these “more appropriate treatments” and people in ICU cannot wait. 

Today, there is no other FDA approved drug to fight against COVID-19. Today, while people may be between life and death, when some do not know how fast and severely they will deteriorate, Plaquenil, which is FDA approved for the treatment and prevention of malaria and for some inflammatory diseases, is still not approved for the treatment of COVID. The FDA ensures the safety and the good use of medications and physicians who today refuse to give Plaquenil, strictly, follow the FDA instructions in your best interest. Is it really so?

The history of Medicine can also teach us lessons. One oral antidiabetic medication (Metformin) was introduced in Europe in 1950 and in the USA in 1995. It took 45 years for the FDA to authorize what turned out to be the basic treatment of diabetes. The first oral anti-diabetes medication was introduced in the USA in 1984. It took 14 years for the FDA to allow american citizens to have tablets instead of insulin shots. It took 12 years for Alexander Fleming to convince his peers that penicillin was not a quackery resulting in the death of hundreds that was avoidable. How many victims from COVID-19 will it take until pragmatic therapeutic approaches are taken? The concept of the patient’s best interest has to be reconsidered in times of crisis. Yes, well-conducted studies are necessary and should guide our medical practice. Sometimes, however, when it is urgent, the risk/benefit ratio may be the only guide. 

The common Plaquenil side effects may include nausea, vomiting, stomach pain or cramps, loss of appetite, weight loss, diarrhea, dizziness, spinning sensation, headache, ringing in your ears, mood changes, nervousness, irritability, skin rash, itching, or hair loss. As to the serious side effects, their frequency according to the medical website Medscape is not well defined. Plaquenil may also cause severe eye damage but only when taken for a long term. This concern is certainly not relevant to a 5 day treatment. Plaquenil may have an effect on the heart visible on an electrocardiogram (EKG) (prolongation of the QT interval) as does Zithromax. The concern is the risk of cardiac  arrhythmia. The risk is even greater when Plaquenil is combined with other drugs that also prolong the QT interval on EKG. A study in 2018 concluded that more studies are needed to evaluate the clinical significance of this EKG abnormality. Pr. Didier Raoult who has used Plaquenil for the past 10 years in his clinical practice and research  writes that the combination of Hydroxychloroquine (Plaquenil) with Azithromycin (Zithromax) was a concern but has not yet been shown to cause EKG problems. An EKG is advisable before starting Plaquenil. Any prolongation of the QT interval requires the approval of a cardiologist to use Plaquenil. In his interview on 03/23/20, the Pr. Raoult speaks of an hypothetical but possible risk of arrhythmia that is more relevant to patients who present with multiple diseases or in the ICU setting.

Drug interaction: Plaquenil may interact with acetaminophen, cancer medications, tuberculosis medications, birth control pills or hormone replacement therapy, arthritis medications, ACE inhibitors, antibiotics, antifungals, cholesterol medications, HIV/AIDS medications, NSAIDs (non-steroidal anti-inflammatory drugs), or seizure medications. 

Side effects must always be correlated with their frequency, and with the risk/benefit ratio. Any medication may have serious side effects. Pr. Raoult, expert in the use of Plaquenil in his interview on 03/23/20 seems to be very annoyed by the warning about side effects and goes up to stating that it is purposely done like to “frighten people with ghosts”. Again, He insists on the fact that several millions of individuals took Hydroxychloroquine over the past 70 years. He does not hesitate to say that the fear of side effects due to Hydroxychloroquine and Azithromycin (Zithromax) does not make sense.

The risks of COVID-19 in a selected population at risk are serious and potentially lethal. In people at high risk of dying from COVID-19, the risk/benefit ratio favors the use of Plaquenil. Pr. Raoult, in his interview on 03/23/20 states that when there is respiratory insufficiency the virus is almost not or no longer detectable. When patients start having severe respiratory insufficiency, when patients are admitted in ICU, it is just too late to initiate Plaquenil. The virus is already gone. It is the remaining inflammation (cytokine storm) that is a life threat. According to the Pr. Raoult Hydroxychloroquine should be initiated when COVID-19 becomes moderate or when patients start getting worse. Plaquenil should be used when the virus is multiplying not when it is almost or totally gone.

Focusing on serious side effects without considering their relative frequency of occurrence and without taking into consideration the immediate life-threatening status and the absence of other alternative therapy causes an unrealistic and unjustified threat and fear on a medication that has the ability to save lives. 

I understand that the authorization to use Plaquenil in the treatment of COVID-19 may lead to unjustified use of this drug where the risk/benefit ratio would not favor the drug, a shortage of this medication and the impossibility to give to those who really need it, for COVID-19 or for other indications. Providers should determine based on their clinical judgment and ethics what to do. However, today people are in ICU, others will have to be admitted in ICUs. These people cannot wait for studies to be completed. 

Alain Mass, M.D.

Board Certified in Family Practice

contact@massfunctionalmd.com

Coronavirus and Plaquenil in the medical literature

https://pubmed.ncbi.nlm.nih.gov/32075365/?fbclid=IwAR1RcuL4O4yFacJ5jRo8Oj0ABJxUsBZamA4rxw8XJ3xGzsAzyR3VPHMJcS4 

https://wattsupwiththat.com/2020/03/17/an-effective-treatment-for-coronavirus-covid-19-has-been-found-in-a-common-anti-malarial-drug/ 

https://www.nature.com/articles/s41422-020-0282-0.pdf 

https://www.ncbi.nlm.nih.gov/pubmed/32150618?fbclid=IwAR07pI0OyQES3nZfrCkHY0qxhX7OUjTuMlmy51nZY6SeUpBwFpVaRnnNYo4 

https://www.mediterranee-infection.com/wp-content/uploads/2020/03/Hydroxychloroquine_final_DOI_IJAA.pdf

https://virologyj.biomedcentral.com/articles/10.1186/1743-422X-2-69

 

 

 

A Fiasco in the Making? As the Coronavirus Pandemic Takes Hold, We Are Making Decisions Without Reliable Data

https://www.statnews.com/2020/03/17/a-fiasco-in-the-making-as-the-coronavirus-pandemic-takes-hold-we-are-making-decisions-without-reliable-data/

The current coronavirus disease, Covid-19, has been called a once-in-a-century pandemic. But it may also be a once-in-a-century evidence fiasco.At a time when everyone needs better information, from disease modelers and governments to people quarantined or just social distancing, we lack reliable evidence on how many people have been infected with SARS-CoV-2 or who continue to become infected. (Article in link)__________________

**Comment**

Key quotes:  

The data collected so far on how many people are infected and how the epidemic is evolving are utterly unreliable.

Reported case fatality rates, like the official 3.4% rate from the World Health Organization, cause horror — and are meaningless.

A population-wide case fatality rate of 0.05% is lower than seasonal influenza. If that is the true rate, locking down the world with potentially tremendous social and financial consequences may be totally irrational. It’s like an elephant being attacked by a house cat.

A positive test for coronavirus does not mean necessarily that this virus is always primarily responsible for a patient’s demise.

_________________

For more:  https://madisonarealymesupportgroup.com/2020/03/21/study-shows-covid-19-testing-as-bad-as-lyme-msids-testing/

https://madisonarealymesupportgroup.com/2020/03/26/what-happens-when-reliable-testing-is-not-available-lessons-from-tick-borne-disease/

https://madisonarealymesupportgroup.com/2020/03/27/cdcs-deadly-testing-fiasco-centralization-of-public-health-authority-a-threat-to-national-security/