For over 25 years my office, The Center for Holistic Medicine located in West Bloomfield, MI, has been effectively treating viral infections. The last few days I have seen the panic that is occurring: schools are closing, college students sent home, and all large events are being cancelled. Rather than a time to panic, this is a time to reflect on our health care system and how to ensure that your immune system is ready to fight COVID-19 (the present coronavirus infection). Conventional medicine’s approach to COVID-19 is suboptimal. They can offer hand washing and quarantining. That is about it. Really, it is pathetic!! Coronavirus is nothing to take lightly. It is also nothing to panic about. Yes, some will get very sick from it. Keep in mind that people get sick from many things. Viruses can cause serious problems. To minimize your risk, follow the instructions I have outlined for you here.
In case you plan to rush out and get a flu vaccine, you might want to read this abstract, and also share with your pro vaccine friends. It appears that getting a flu vaccine will make you more prone to coronavirus infection. This is hot off the press. My interpretation of this is that when you receive (or your child) a vaccination, your immune system is artificially deranged by the vaccine so that it will not respond normally to secondary challenge. This is one of the missing elements in alleged vaccine research. A vaccine "interferes" with the immune system's normal processes. The first sentence in the abstract says it all: "...vaccination may increase the risk of other respiratory viruses, a phenomenon known as vaccine interference" Please read. My heart goes out to the millions of children whose immune systems have been tampered with by forced vaccination.
The childhood vaccine schedule in the U.S. features numerous combination vaccines—formulations that bundle multiple antigens for multiple diseases into one injection. Examples of combination vaccines currently given to American children include Merck’s four-component ProQuad vaccine against measles, mumps, rubella and varicella and Sanofi’s five-in-one Pentacel vaccine against diphtheria, tetanus, pertussis, polio and Haemophilus influenzae type b. Now, the U.S. is preparing to up the combination vaccine ante still further. At the close of 2018, the FDA approved the nation’s first six-in-one (hexavalent) vaccine—a Merck and Sanofi joint effort called Vaxelis intended for infants at ages two, four and six months. Like hexavalent vaccines given to infants in other countries, Vaxelis combines the five components featured in Pentacel along with Merck’s genetically engineered Recombivax vaccine against hepatitis B (HepB). What about hexavalent vaccine risks, publicized in other countries for decades? On that topic, the CDC and FDA have been largely silent, perhaps because of the next-to-useless design of the U.S. Vaxelis clinical trials, which compared one heavily vaccinated group against another—rather than comparing Vaxelis against an inert placebo. Unsurprisingly, this bogus procedure allowed researchers to conclude that adverse reactions to the vaccines were similar across groups. In other words, “nothing to see here.” Before U.S. agencies open the floodgates for hexavalent vaccination, they would do well to remember that “public trust can be lost only once and not acting or acting too late on a [safety] signal . . . could damage credibility of those supporting and maintaining vaccination for many years.”
Medical Doctor Complains that He Cannot Test His Patients for Coronavirus Because CDC will Not Provide Same Test Kits Used in Other Countries
I just finished a busy week seeing patients. During this time, I saw at least six patients who had flu-like illnesses. Did they have COVID-19? I don’t know. Why don’t I know? I can’t tell my patients if the are sick with coronavirus because there are no test kits available to me. However, test kits are widely available in many other countries including Iran, Japan, South Korea, Germany, or China. In fact, hundreds of thousands of coronavirus tests have been run in other countries. But, NOT in the US. As of Monday, March 2, 2020, the US has tested a few hundred people for coronavirus. According to the CDC, 337 more kits were released on Tuesday and Wednesday this week. Why are other countries able to test for coronavirus and we aren’t?!?! We are clearly getting cheated when it comes to healthcare. And, the CDC is very good at cheating us. They cheated us by stealing $1 billion dollars for the Zika non-epidemic. Now, they will get paid handsomely for their missteps with coronavirus.
The World Health Organization (WHO), a pair of articles recently published in The BMJ have revealed, is sponsoring an experimental study of a controversial malaria vaccine among African children without obtaining informed consent from parents. Data from prior clinical trials of the vaccine, manufactured by the British multinational pharmaceutical corporation GlaxoSmithKline (GSK), have shown it to be associated with an increased risk of clinical malaria after four years, a tenfold increased risk of meningitis, an increased risk of cerebral malaria (in which the parasitic organisms block the flow of blood to the brain, causing swelling and potential brain damage), and an increased risk of death that was disproportionately higher for female children. Concerningly, apart from failing to properly inform parents about the risks or even letting parents know that their children are being experimented upon, the WHO intends to make a decision based on this trial about whether to recommend the vaccine for routine use throughout sub-Saharan Africa after just twenty-four months of study, which is not enough time to determine the vaccine’s effect on mortality. This is especially concerning in light of scientific research showing that other non-live vaccines—such as the diphtheria, tetanus, and whole-cell pertussis (DTP) vaccine—are associated with an increased rate of childhood mortality. The WHO, however, has dismissed this evidence and continues to recommend the DTP vaccine for routine use in children in developing countries. The behavior of policymakers at the WHO, while highly alarming, is not at all surprising given the organization’s conflicts of interest, including industry funding and members of its vaccine advisory group having financial ties to pharmaceutical companies. It should be of great concern to every free-thinking inhabitant of this planet that the WHO and UN, along with state governments around the world, are pushing for an ever-increasing number of childhood vaccinations while ignoring scientific evidence that doesn’t suit their political and financial agendas and while prejudicing the individual right to informed consent.
A new study published in the open access Systematic Reviews journal titled Benefits and harms of the human papillomavirus (HPV) vaccines: systematic review with meta-analyses of trial data from clinical study reports attempts to tackle the controversial vaccine. Using clinical study reports obtained from the European Medicines Agency (EMA) and GlaxoSmithKline from 2014 to 2017, study authors Lars Jørgensen, Peter Gøtzsche and Tom Jefferson set forth to assess the benefits and harms of the HPV vaccine. The researchers looked at twenty-four of 50 eligible clinical study reports containing 58,412 pages of 22 trials and 2 follow-up studies including 95,670 participants: 79,102 females and 16,568 males age 8–72. The newly published research from Gøtzsche and co-authors found more of the same shoddy research behavior reporting: “Serious harms were incompletely reported for 72% of participants. Nearly all control participants received active comparators. No clinical study report included complete case report forms.” Furthermore, the researchers found: “the HPV vaccines increased serious nervous system disorders and general harms.”
The headline in the February 25, 2020 article in the New York Times article reads, “How to prepare for the Coronavirus.” Right below the headline, in large font, it states, “Wash your hands. Keep a supply of medicines. Get a flu shot.” I have no problems with the idea of washing hands. That is a good antimicrobial technique. As for keeping a supply of medications, the author of the article is making the point of having a 30-day supply of medications on hand in case you cannot go out to get them. I have no issue with that advice. Get a flu shot? WHAT? WHERE DID THAT COME FROM? The writer states, “Infectious disease specialists strongly recommend flu vaccination. And the best protection for older people against bacterial pneumonia is, paradoxically, to vaccinate children…” Folks, this is another example of FAKE NEWS! The flu vaccine has never been shown to protect against pneumonia. I would suggest the opposite is true; those who get the flu vaccine will be more at risk for other non-flu-like infections such as coronavirus.
We can all agree that 50 tons of vitamin C pretty much qualifies as a megadose. We can also likely agree that trucking 50 tons of vitamin C, straight into Wuhan, full in the face of the COVID-19 epidemic, qualifies as news. The news media are not reporting this, or any other, significantly positive megavitamin news. We are so used to being lied to that the truth is like a diamond in a five-and-dime store: you can't believe it is real because it is mixed in with the fakes. News of nutrition-centered treatment of COVID-19 has been branded "fake news" and "false information." I say that what is "false" and "fake" is the deliberate omission of any news of health-saving, life-saving measures already underway to help the people of China and the rest of our planet.
Do We Need $2.5 BILLION for Coronavirus Vaccine? What Happened to the $2 BILLION Spent on the Zika Vaccine?
The White House is asking Congress for AT LEAST $2.5 billion in emergency funds, in part, to develop a vaccine for the Coronavirus outbreak. Before we give any governmental agency AT LEAST $2.5 billion dollars we should know how it is going to be spent. Recall the Zika scare from 2016. At that time we were being told by the US governmental agencies (FDA, CDC, and HHS) that somehow a relatively benign virus that has been around for nearly 100 years was suddenly causing birth defects in the form of small-headed babies. Congress ended up giving the CDC over $1 billion dollars to develop a Zika vaccine. Here we are 4 years later and…no Zika vaccine and no more reports of small-headed Zika infections. The reason there are no more reports is because Zika did not cause the problem in the first place. Zika is still occurring around the world and we are still surviving—without an epidemic of small-headed babies. The CDC should be the last governmental organization trusted with AT LEAST $2.5 billion dollars to study COVID-19. The CDC has consistently lied and hid data that shows our kids are suffering adverse effects from receiving too many vaccines. The CDC is the same organization that refuses to complete a study comparing children fully vaccinated against those unvaccinated. That study would provide the final answer to whether too many vaccines are harming our children. The CDC was tasked with that study decades ago and has the available data available, and yet…we still have no study.
On May 24, 2019, Maine’s House of Representatives passed a bill (LD798) removing religious and philosophical vaccine exemptions to block Maine residents from getting an education in a public, private, parochial or trade school or enrolling in educational courses online. The bill was strongly opposed by grassroots health freedom groups and passed the state Senate by only one vote. Unless it is vetoed by Maine voters in a ballot vote on Mar. 3, 2020, the new law will go into effect on Sept. 1, 2021. Mainers for Health and Parental Rights, a political action committee (PAC), filed paperwork with the state for a veto ballot referendum that would overturn the vaccine exemption repeal. In September 2019, the campaign filed 95,871 raw signatures, of which 79,056 were valid, exceeding the minimum of 63,067 signatures needed. On October 17, 2019, Maine Secretary of State Dunlap announced that the veto referendum qualified to appear on the ballot at the statewide election on March 3, 2020.