I know you can’t see me but tears are running down my face as I think about you. The following quote comes to mind:
“You is kind. You is smart. You is important.” ― Kathryn Stockett, The Help
Although this was said from a maid to a little girl, we never outgrow the need for affirmation and this is most certainly true if you are a woman chronically infected with tick-borne illness, have a child with tick-borne illness or you are one in the growing army of women who while being infected yourself, care for an infected menagerie at home.
It’s been shown studies have been rigged for a pre-determined outcome
Some fraudulent studies have been retracted but many more remain.
Dr. Didlier Raoult states the RECOVERY Trial was “the Marx Brothers doing science,” and that the person in charge of the trial (Professor Landray from Oxford) used the “usual” dosage for amoebic dysentery – which HCQ isn’t usually used for. He states that Landray does not understand anything about infectious diseases or anti-infection drugs, but led an international trial anyway.
A Yale epidemiologist is on record stating that Fauci is running a misinformation campaign against HCQ.
Here’s another well written article picking apart the Big Pharma sponsored Together Trial being used to discredit cheap generic treatments. A complicit media then blasts out click bait headlines to an unsuspecting public.
This thorough article states that the trials for generic antivirals show systematic, egregious selection bias, as well as highlights the success in virtually eradicating COVID in countries who buck WHO instructions and used ivermectin prophylactically.
Authorities gave the anti-viral drug remdesivir an emergency use authorization (EUA) while requiring two months of successful use of hydroxychoroquine in China and South Korea to get a similar EUA. We keep being told HCQ needs to be in a large double-blind placebo controlled study because it has scary side-effects, despite being used safely for decades – even over the counter! The same is true for ivermectin. Why are they suddenly dangerous?
Please know remdesivir, which is truly ineffective against COVID, has horrific side effects, including liver toxicity but is the “golden child” of authorities due to profits. Here’s the facts:
There were more than 500 deaths in the first year of remdesivir usage.
There have been 20 deaths in 19 years of ivermectin usage.
Yet, according to a FOIA request that proved the CDC can not prove even ONE COVID death in children younger than 16, the FDA has now approved remdesivirfor babies! Here’s the facts:
Gilead, the manufacturer of remdsivir, announced by press release, (which appears to be the way science is now done in the ‘new normal) that there was clinical improvement at day 10.
The study conveniently has no control group, making it impossible to compare effectiveness against standard of care and only included 53 children – three of whom died.
Adverse events were reported in 72% of the children, with 21% experiencing serious adverse events:
elevated levels of liver enzymes
allergic reactions
fever
shortness of breath
rash
nausea
sweating
shivering
The drug is marketed under the name Veklury, but the clincher is that similarly to the COVID injections which are in a current clinical study with those receiving the injections being test subjects, a clinical study on infants using Veklury is also underway and also will not be completed until 2023. Is it really wise to allow an out of control, corrupt, conflict-riddled government agency to use your child as a test subject?
This article goes through 5 studies the FDA uses to support remdesivir. All of them show little if any benefit to hospitalized patients with moderate or severe disease. It’s important to note that none of these studies looked at children or infants and only 8 subjects were under 18 – which means the FDA has ZERO data to support remdesivir in children.
And please see this article where France’s long-time vaccine policy chief delineates how COVID policy is “completely stupid” and “unethical,” and clarifies that hundreds of publications prove that early treatment works and how trials have been rigged.
Nitpicking and blackballing treatments is common with Lyme/MSIDS too.
In the case of COVID-19, severe patients can quickly die, making treatments desperately needed now, not in six months. One doctor has stated that Big Pharma’s suppression of ivermectin has cost 500,000 lives.
Doctors and pharmacists go to school to learn about drugs and their interactions. How about ‘authorities’ just let doctors do their jobs? I don’t see these ‘authorities’ condemning severely toxic cancer treatments which kill as many good cells as bad cells.
Why the focus on HCQ & ivermectin?
One good reason is its effectiveness not only against COVID but against other viruses as well.
This recent article also explains another reason why. In essence, the CDC is in bed with Gilead Science as nine of the experts on the NIH COVID-19 Panel recommending treatment options have disclosed financial support from Gilead.
Gilead Science created the anti-viral remdesivir which was unsuccessful for Ebola. They then dug it out of the drug graveyard and pushed it for COVID-19 to make up for lost profits.
HCQ and ivermectin, even though they’re clinically showing great success, stand in the way of their chosen profitable treatment.
So there you have it. This is what our authorities care about. Profits.
The following video created by a Canadian does an excellent job of editing multiple videos together showing the big picture of what’s going on with COVID-19. After the article I show Fauci’s patents – which are numerous and include patents regarding OspA –which should perk up ears of Lyme/MSIDS patients.Nearly every Lyme vaccine to come out revolves around OspA(outer surface protein A).
Here is my latest video on the uncovering of millions of $$ sent to the Wuhan lab under the control of Dr. Fauci and in Canada, Trudeau sent hundreds of thousands of $$ which helped create the crisis we are facing. Dr. Tam continues to mishandle the situation as she places her loyalty to the World Health Organization over the citizens of Canada. Where does her loyalty lie? It’s time to fire Dr. Fauci … and … Dr. Theresa Tam.
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**Comment**
Dr. Fauci doesn’t need to only be fired. He needs to be held accountable for his crimes and put in jail.
Fauci’s patent for the treatment of OspA-stuck-on-anything: U.S. Patent No. 5,696,079He also makes a decent salary in this business of abusing sick and disabled people: Fauci salary
Lastly, the media has been complicit in all of this. They are not questioning the draconian measures being taken or the disagreement in the medical community. If they do show the “other side” they cast a bad-light upon it. In fact, much has come out showing they continue to twist facts or make them up entirely(falsely showing footage taken in Italy and claiming it was taken here as well as staging an event to make it look worse than it is). They claim it was an “editing” mistake. I’ve worked in TV and that type of mistake isn’t made!https://madisonarealymesupportgroup.com/2020/05/06/expose-cbs-michigan-health-center-workers-stage-fake-patients-in-covid-19-testing-watch-it-quickly-before-its-yanked/
Recently I posted another fantastic Canadian article which discussed Event 201, a global pandemic exercise simulation of a factitious new coronavirussponsored by Bill and Melinda Gates, World Economic Forum and the Center for Health Security at Johns Hopkins. They discussed what to do about “misinformation” on the internet.
Excerpt:
Hasti Taghi chief of staff capacity at NBC Universal, noted that the anti-vaccine movement was very strong due to social media and therefore, they need to disseminate “the right information….to ensure the public has trust in the vaccines that we’re creating” against COVID-19. Harrington agreed stating this recent strong resistance was a “beta” test for dealing with resistance to COVID-19 vaccines. Also in attendance at Event 201 was Avril Haines, past assistant to the president and Principal Deputy National Security Adviser for the Obama administration, Deputy Director of CIA, Legal Advisor to National Security Council, who suggested daily briefings would work better than trying to control information to “flood the zone” from “trusted sources”at every level by community and faith based leaders and health care officials. Harrington agreed and added the need to educate trusted local leaders in advance of a pandemic to ensure readiness.
Four months after Event 201 COVID-19 information started flowing simultaneously from the media showing COVID-19 to be the most serious threat to humanity.
Fauci, Birx and Redfield, all incestuously complicit in the HIV/AIDS frauds and malpractice, today hold the future of not only American public health, but also of the entire world economy in their hands. Not a good situation. As their work on the proved HIV=IDS fraud shows, the coronavirus tests do not at all prove presence of a deadly virus in any patient. If this is so, it is perhaps the greatest criminal fraud in medical history.
This is not a conspiracy theory. It’s a conspiracy. Period.
The U.S. Food and Drug Administration has learned that some ranitidine medicines, including some products commonly known as the brand-name drug Zantac, contain a nitrosamine impurity called N-nitrosodimethylamine (NDMA) at low levels. NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests. NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products, and vegetables.
The FDA has been investigating NDMA and other nitrosamine impurities in blood pressure and heart failure medicines called Angiotensin II Receptor Blockers (ARBs) since last year. In the case of ARBs, the FDA has recommended numerous recalls as it discovered unacceptable levels of nitrosamines.
When the agency identifies a problem, it takes appropriate action quickly to protect patients. The FDA is evaluating whether the low levels of NDMA in ranitidine pose a risk to patients. FDA will post that information when it is available.
Patients should be able to trust that their medicines are as safe as they can be and that the benefits of taking them outweigh any risk to their health. Although NDMA may cause harm in large amounts, the levels the FDA is finding in ranitidine from preliminary tests barely exceed amounts you might expect to find in common foods.
Ranitidine is an over-the-counter (OTC) and prescription drug. Ranitidine is an H2 (histamine-2) blocker, which decreases the amount of acid created by the stomach. Over-the-counter ranitidine is approved to prevent and relieve heartburn associated with acid ingestion and sour stomach. Prescription ranitidine is approved for multiple indications, including treatment and prevention of ulcers of the stomach and intestines and treatment of gastroesophageal reflux disease.
The agency is working with international regulators and industry partners to determine the source of this impurity in ranitidine. The agency is examining levels of NDMA in ranitidine and evaluating any possible risk to patients. The FDA will take appropriate measures based on the results of the ongoing investigation. The agency will provide more information as it becomes available.
The FDA is not calling for individuals to stop taking ranitidine at this time; however, patients taking prescription ranitidine who wish to discontinue use should talk to their health care professional about other treatment options. People taking OTC ranitidine could consider using other OTC medicines approved for their condition. There are multiple drugs on the market that are approved for the same or similar uses as ranitidine.
Consumers and health care professionals should report any adverse reactions with ranitidine to the FDA’s MedWatch program to help the agency better understand the scope of the problem:
Download and complete the appropriate form, then submit it via fax at 1-800-FDA-0178
The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.
The next time a tick feeds on you, Washington State University researchers hope to make sure persistent arthritis caused by Lyme disease doesn’t linger for a lifetime.
Troy Bankhead, associate professor in WSU’s Veterinary Microbiology and Pathology department, and his team have spent more than a decade analyzing an immune evasive protein of Borrelia burgdorferi, the bacterium that causes tick-borne Lyme disease.
With the lab’s latest finding, that work is beginning to pay off.
According to research recently published in Cell Reports, Bankhead and assistant research professor Abdul Lone discovered that a surface protein known as VlsE acts as a shield to prevent the immune system from effectively fighting the disease. In particular, the study examined how VlsE protects one of the main proteins responsible for Lyme disease’s persistent arthritis.
“This really has a significant impact in the development of vaccines,” Bankhead said. “If we can determine which proteins are shielded as opposed to which ones are not, then of course those that are not protected are going to be better candidates for a vaccine.”
The Centers for Disease Control and Prevention estimates some 300,000 people may get Lyme disease each year in the United States alone. It is most prevalent in the northeast.
If not treated early with antibiotics, Lyme disease can cause lifelong arthritis, and in more severe cases, bladder infections, heart inflammation, and neurologic and cognitive issues like loss of memory and balance.
“We chose the arthritis-related protein because arthritis is the most common symptom you see in North America,” Lone said.
By engineering a strain of Borrelia burgdorferi in the lab without the surface lipoprotein VlsE, they were able to confirm it was protecting the arthritis-related protein from an antibody response.
Bankhead and Lone tested the new Borrelia strain in mice and found the animals were more easily able to clear the infection.
Then, Bankhead and Lone confirmed that the new Borrelia strain was susceptible to antibodies under the microscope.
By using fluorescence microscopy, a process that uses energy from electrons to emit light under a microscope, Bankhead and Lone watched as antibodies were unable to bind to the protein responsible for Lyme’s persistent arthritis when the VlsE protein was present. When the VlsE protein was removed, antibodies were able to recognize and bind to the arthritis-related protein.
“When you don’t have VlsE those bacteria light up and that is because those antibodies are able to bind and recognize that arthritis-related protein in the absence of that VlsE shield,” Bankhead said. “That’s exactly what we were seeing.”
Understanding the VlsE protein is acting as a shield for the bacterium’s arthritic-causing protein is significant for vaccine development and future research. While it is unknown if other surface proteins are protected, Bankhead said it is likely. He noted the scientific community is gaining ground on understanding these proteins but producing any vaccine is well into the future.
Still, the finding creates two avenues for researchers to eliminate Lyme disease:
take down the VlsE shield, or,
find a way for the antibody response to get in front of the ever-adapting bacterium and eliminate it.
“HIV/AIDS persists for years in human beings. The same thing happens with Borrelia, it persists,” Lone said. “While this finding tells us a lot about Borrelia. Our next step is to understand how it persists. Once we understand the mechanism of persistence, we can eliminate the disease.”
Media contacts:
Troy Bankhead, WSU College of Veterinary Medicine, tbankhead@wsu.edu
Laura Lockard, WSU College of Veterinary Medicine, 206-861-6884, laura.lockard@wsu.edu
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**Comment**
From where I sit, the saga of HIV/AIDS us far from conclusive. Similarly to the Cabal that myopically focused on amyloid,to the exclusion of all other potential causes, in regards to Alzheimer’s, there was a Cabal focusing solely on a “supposed” HIV virus that has yet to be truly (singularly) isolated with proof of an electron micrograph. This is also true of nearly every other virus being blamed for “pandemics” by authorities.
To date there are researchers who have held their ground that HIV does not cause AIDS – losing all in the process. I think we should take people like that seriously. They have everything to lose and nothing to gain by continuing to hold a stance that flies in the face of the narrative – similarly to Lyme doctors. Many have stood up in opposition to a virus causing AIDS: http://www.virusmyth.com/aids/group.htm
