Fact Check: COVID-19 Cured.
Ivermectin-based treatments have cured hundreds of thousands of COVID-19 infected patients worldwide. Ivermectin has also successfully protected thousands of doctors who have been treating COVID-19 infected patients. As the evidence throughout this report reveals, scientific studies and clinical trials have proven that Ivermectin-based treatments kill the SARS-CoV-2 virus in humans with little, if any, side effects.
The antiviral action of Ivermectin makes it a safer, less expensive and more effective way to deal with viruses than vaccines. In fact, Ivermectin makes many vaccines unnecessary.
The best news of all, Ivermectin is inexpensive, readily available and well over one billion people throughout the world have safely taken it.
Ivermectin has a storied history as a “wonder drug.” It has been around for over 45 years and has a long-proven safety profile earning a place on the World Health Organization’s list of essential medicines. It is also commonly given to children to safely treat head lice. In addition, throughout the United States alone over $1 billion per year of Ivermectin is given to animals safely.
In 2004, the World Health Organization issued a bulletin headlined, “Mass treatment with Ivermectin: an underutilized public health strategy,” which states, “It is time to capitalize on the full public health potential of Ivermectin.” Based on the latest studies in response to the COVID-19 virus, Ivermectin’s potential is now being realized.
Triple Therapy COVID-19 Cure: Ivermectin, Zinc and Doxycycline
The Ivermectin, Zinc and Doxycycline triple therapy treatment was developed by internationally renowned physician and Australia's Centre for Digestive Disease (CDD) Medical Director Thomas Borody. He already has four FDA approved drugs and is famous for developing a triple therapy cure for peptic ulcers, which saved millions of people worldwide. He used the same methodology to come up with this Ivermectin-based treatment.
“I am supporting the Ivermectin, Zinc and Doxycycline treatment because it has very few side-effects and is a real killer of coronavirus.”
“This drug works both as a preventative from infection and as a cure for people who are already suffering symptoms."
“It is an anti-parasitic. It is used across South America, the U.S.A., India and Bangladesh. In those place, trials were done. The amazing and surprising thing is, there is not one paper where it was successful less than 100%. That’s not very easy to believe, because it is just too good to be true. Nevertheless, that is the actual factual result. It is curative within 6 to 8 days.”
“There are so many doctors who take it around the world, and don’t tell you about it until you ask them, as a preventative for themselves not to catch it, because often they are frontline workers…. I take it myself.”
“I have doctors in Australia who take it. There are so many [doctors] in the U.S. who take it, and it doesn’t come out in the news.”
“I speak with people in the U.S. who are physicians who developed COVID and within 24 hours [after taking it] their symptoms disappear. It is a very rapidly acting treatment in clinical medicine.”
“It is not covered in the media because there is no big pharmaceutical company behind it…. I am not going to make any money out of this… because it is cheap, it is rapidly available now, we will not run out of it… but there is no huge pharmaceutical companies behind it… so it just didn’t get a lot of airing [on mainstream news outlets].” ~ Dr. Thomas Borody, CDD Medical Director
Here is Dr. Borody describing how the treatment works:
“The main thing about it, it is safe. It has been around since 1975 and it is broad spectrum; it kills viruses, bacteria and parasites. Especially in a test tube, it was 5000 times more powerful than anything else.”
“The trouble was, it was a high dose in a test tube. So, what we added to it was an anti-biotic that is also anti-parasitic and anti-viral, which is Doxycycline. We could then reduce the dose, and add a general endosome-active agent called Zinc, and we were surprised at how amazingly well it cures coronavirus.”
“I am speaking as a person who repurposes multiple drugs for killing intracellular, inside cells, bacteria and viruses.”
“This Ivermectin and others inhibit intracellular proteins that help this virus multiply in our cells, because they cannot multiply on their own. They have to enter our cells, and that’s where you nab them.”
“As Mount Sinai Hospital just published, Ivermectin blocks the landing sights on the spike of the receptors called AC2 receptor throughout the lungs and the gut, and secondly, it inhibits replication within the cell by using Zinc which it forces or helps to get in the cells…. The Doxycycline helps in those two areas as well.”
“The threat production stops, stops dead, and I am still surprised how well it works, and how few side effects that it has.”
"There are a number of studies that are amazingly successful. In fact, we haven't seen a result that is under 100%. We've used it in the United States. We had a 14-hospital trial in Bangladesh and we got 100 out of 100 [cured]. In China, they reproduced it and got 60 out of 60 cured.”
All three medicines in this triple therapy are already FDA-approved and readily available. We can start taking it en masse now; as Dr. Borody sums it up:
“These three medications are already approved. They do not need pre-clinical or clinical trials nor additional TGA approvals….”
“An Ivermectin tablet can cost as little as $2 – which could make it by far the cheapest, safest, and fastest cure.”
"We should identify anyone who is positive and treat them, and those who are around them, give them a half dose preventative treatment.”
“Those who are on the frontlines should all be given the preventative treatment because the side effects are so miniscule.”
“I don't know why we haven't started treating before. The drug has been around so long. We know it is safe to use.”
For more information on this proven effective COVID-19 treatment protocol, read this report.
Fact Check: Large pharmaceutical companies, corrupted officials, the mainstream media, Google and Facebook are trying to suppress life-saving treatments and information on cures to COVID-19.
Large pharmaceutical companies, who stand to lose over a trillion dollars in revenue, along with corrupted government and “health” officials are suppressing Ivermectin-based life-saving treatments. In addition, the mainstream media, Google and large social media companies are proactively censoring information on Ivermectin’s success in curing COVID-19 patients.
Even though the Ivermectin combination includes three proven safe and effective medicines, government agencies are slowing and proactively trying to prevent wide-scale distribution by falsely claiming that it is unproven and unsafe, and based on past actions they will most likely try to rig those studies, as they did with proven effective Hydroxychloroquine (HCQ) treatments, because these are inexpensive and readily available medications that large pharmaceutical companies cannot cash in on.
Ivermectin-based treatments have already cured hundreds of thousands of COVID-19 patients with minimal, if any, side effects. When compared to the FDA Emergency Use Authorization (EUA) approved COVID-19 drug Gilead Sciences’s Remdesivir, Ivermectin treatments have been clearly proven to be much safer and much more effective, while also being much more readily available for a tiny fraction of the cost.
As we know from the proven corrupt COVID-19 Treatment Guidelines Panel approval process, which is dominated by pharmaceutical industry members who voted to shutdown life-saving HCQ treatments in favor of the less effective, more dangerous, and highly profitable Remdesivir drug, getting this Ivermectin combination approved through them for wide-scale distribution appears unlikely.
In fact, in response to Ivermectin’s growing momentum, the most recent release from COVID-19 Treatment Guidelines Panel “recommends against the use of ivermectin for the treatment of COVID-19, except in a clinical trial.” Their stated rationale behind this decision is a reiteration of the misleading claims made in articles and “fact” checks that this report has previously referenced:
“Ivermectin has been shown to inhibit the replication of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in cell cultures. However, pharmacokinetic and pharmacodynamic studies suggest that achieving the plasma concentrations necessary for the antiviral efficacy detected in vitro would require administration of doses up to 100-fold higher than those approved for use in humans. Even though ivermectin appears to accumulate in the lung tissue, predicted systemic plasma and lung tissue concentrations are much lower than 2 µM, the half-maximal inhibitory concentration (IC50) against SARS-CoV-2 in vitro.
Ivermectin is not approved for the treatment of any viral infection, including SARS-CoV-2 infection. The FDA issued a warning in April 2020 that ivermectin intended for use in animals should not be used to treat COVID-19 in humans.”
Once again, Dr Borody’s triple therapy treatment allows for a much lower, safe and effective dose. In addition, thousands of doctors have safely given hundreds of thousands of COVID-19 patients much lower doses with success. The COVID-19 Panel, the FDA and mainstream media outlets also continually try to mislead people by giving the impression that Ivermectin is only used on animals, which is obviously absurd because billions of people, including millions of children, have safely and effectively taken it.
Other than the COVID-19 Panel and the FDA, the usual suspects are once again abdicating their journalistic and ethical responsibilities by repeating Big Pharma misinformation. The World Health Organization, The NY Times, The Guardian, ABC, The Conversation, The National Interest and “fact” checking websites have already published scandalously misleading information in an attempt to discredit Ivermectin as an effective COVID-19 treatment.
Not surprisingly, when you look at the financial disclosures from COVID-19 Treatment Guidelines Panel members, you will see that eight of them are paid by Gilead Sciences, the makers of the panel-approved drug Remdesivir. Several other panel members also have financial ties to large pharmaceutical companies. There are two members paid by Merck, one by INOVIO, one by AstraZeneca and Eli Lilly, among others. These are blatant conflicts of interest that are clearly leading to the suppression of life-saving inexpensive medicines and resulting in thousands of unnecessary deaths.
These people need to be prosecuted for Crimes Against Humanity.
How many more people will have to die unnecessary deaths?
An analysis of the data demonstrates that suppression of HCQ in the United States has already led to 145,965 unnecessary deaths.
When you compare national death totals between countries that allowed widespread HCQ use to countries that blocked HCQ usage, you find countries that allowed HCQ had a 76.8 percent lower death rate. As of September 4th, the United States has officially reported 190,058 COVID-19 deaths; 76.8 percent of that total equals 145,965 unnecessary deaths.
Here is a brief summary of this analysis:
“Early treatment with hydroxychloroquine: a country-based analysis
We investigate early or prophylactic treatment for COVID-19 with hydroxychloroquine (HCQ), which has been adopted or declined in different countries. Since the severity of COVID-19 varies widely based on age and comorbidities, treatment was generally only initiated in higher risk individuals. The primary endpoint was death….
Many countries either adopted or declined early treatment with HCQ, effectively forming a large trial with 1.8 billion people in the treatment group and 663 million in the control group.
As of September 3, 2020, an average of 55.2 per million in the treatment group have died, and 461.9 per million in the control group, relative risk 0.120. After adjustments, treatment and control deaths become 114.9 per million and 684.1 per million, relative risk 0.17.
The probability of an equal or lower relative risk occurring from random group assignments is 0.008. Accounting for predicted changes in spread, we estimate a relative risk of 0.23.
The treatment group has a 76.8% lower death rate.
Confounding factors affect this estimate. We examined diabetes, obesity, hypertension, life expectancy, population density, urbanization, testing level, and intervention level, which do not account for the effect observed.”
You can read this full analysis and see source data, which is updated daily, at HCQtrial.com.
To make matters even worse, three studies that were used to discredit and prevent use of HCQ have been exposed as being rigged. The Lancet retracted their fraudulent study because it was based on “fabricated data.” The WHO clinical trials were exposed as giving 3500 COVID-19 patients at 400 hospitals throughout 35 countries “non-therapeutic, toxic and potentially lethal doses of HCQ.”
Most disturbing of all, in another clear example of Crimes Against Humanity, a study at Oxford University that was conducted in partnership with the WHO HCQ trials, which was sponsored by the GlaxoSmithKline and the Bill and Melinda Gates Foundation, also gave extremely high doses to 1,542 COVID-19 patients and 396 of them died.
Fortunately, as of right now, the Ivermectin combination includes three medications that are already FDA approved, so it does not need an FDA EUA or COVID Panel approval for current practitioner prescribed use and are readily widely available. Of course, as always, consult your doctor before using it.
To reiterate, the censorship, suppression and false discrediting of HCQ treatments by government agencies and the mainstream media, and the recent suppression of Ivermectin, clearly demonstrates their desire to put pharmaceutical profits before American lives, which unequivocally amounts to Crimes Against Humanity.
The pharmaceutical industry spends twice as much as any other industry lobbying congress. They have captured “regulatory” agencies, including but not limited to: the CDC, NIH, NIAID, HHS, FDA and both the Republican and Democratic parties. In addition, pharmaceutical industry sponsorship and advertising are the largest revenue drivers for mainstream “news” outlets.
Beyond mainstream “news” outlets, Alphabet, Google and YouTube’s parent company, now has two other large subsidiaries, Verily and Calico, which are pharmaceutical companies who have partnered with many of the largest companies in the industry. Therefore, Google and YouTube’s censorship and suppression of inexpensive COVID-19 treatments and any information that is critical of their partners expensive medications and the highly profitable “vaccination” program, demonstrates a clear conflict of interest.
Other than Google and YouTube’s conflict of interest, social media companies and popular “fact” checking websites are funded by and/or have partnered with foundations that are run by people who will make billions of dollars profiting off expensive COVID-19 medications and the “vaccination” program.
* In an upcoming extensive report, we will analyze how Pandemic Profiteers effectively influence the media and control the official COVID-19 narrative. (subscribe here for updates)
“A vaccine doesn’t cure or prevent occurrence. There are papers that show a vaccine loses its activity between three and six months, so we are in trouble with a vaccine.”~ Dr. Thomas Borody, CDD Medical Director
The bottom line, as the evidence throughout this report reveals, we now have a proven prophylactic (preventive) treatment and COVID-19 cure. If this life-saving medicine is not widely distributed now, the interests suppressing this treatment and censoring information on it are clearly complicit in Crimes Against Humanity.
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