Vaccines are never designed to kill or disable people. The background death rate for vaccination in the US is <500 people per year and that’s because people coincidentally die around the time of the vaccination.
The death toll for the current vaccines in the US alone is well over 5,000 so far, and that’s likely a very conservative estimate because the data is under reported historically and even more so during the pandemic (based on all the anecdotes I’m aware of because nobody wants to challenge the narrative that the vaccine is anything but safe). Note that a comparable % of Americans have been vaccinated with the COVID vaccine as compared with prior years. This vaccine is more than 100X more deadly than the flu vaccine… possibly even 1,000 times more deadly.
The CDC cannot explain any of the 4,500 excess deaths. If it wasn’t the vaccine, what caused it? Have you seen the analysis of any of these cases? They cannot explain how dozens of our children have heart problems now. They will not disclose how many dozens of kids are affected. 10 dozen? 100 dozen? They will not tell us the truth. The one thing all those 4,500 deaths had in common was the vaccine.
No numbers are disclosed on deaths or any other adverse side effects. There’s a reason for that: they have no clue what the numbers are. That alone should be frightening.
Not only won’t they tell us the numbers, but they aren’t answering any questions either: nobody is willing to debate the top issues raised in this article in a public forum.
So now after killing more than 4,500 Americans, the government wants to “protect” your children knowing full well that some of them will die from a vaccine that is totally unnecessary and dangerous. It is preposterous and no parent should put up with it.
This vaccine is much more dangerous than any vaccine in our history. There are more reactions to this vaccine than all 70 vaccines in the last 30 years combined. This is obvious from OpenVAERS since the total reports from this vaccine and # of deaths are rapidly approaching >50% of all reported cases. Note that VAERS is a lagging indicator because here is a substantial backlog of VAERS reports. As of 28 May, there were 262,566 reported adverse reactions regarding Covid-19 vaccinations. However, there was another 168,564 reports that have been submitted to VAERS but not added to the database yet.
The vaccine teaches cells all over your body (every organ especially women’s ovaries) to make a toxic spike protein.
Over 4,500 people have been killed by this “safe” vaccine. If a foreign nation killed well over 4,500 Americans, would we sit idly by and cheer them on? The government might argue that the death toll is less than the 600,000 Americans who have died from the virus. But that’s a false argument because our government has been deliberately suppressing the alternatives (despite proof of efficacy in large randomized Phase 3 trials) and keeping them from view.
It is almost beside the point to calculate the exact number of deaths. In the past, the death threshold was that if 1 in 1 million Americans were killed by the vaccine, we stop it. So we stop at 168 excess deaths. There are 4,500 excess deaths right now and probably more like 25,000. So we are at 25X to 125X over the stopping threshold and we want to accelerate our rate of vaccination and give it to our kids. Why isn’t the press asking why we are doing this when there are better alternatives that result in much lower loss of life?
We don’t know how many people have died. 4,500 is a lower bound. And many more will be temporarily or permanently disabled. Nobody is talking.
Based on all the anecdotal reports from physicians I’ve received so far, I estimate the severe life altering side-effects rate to be around 4% and the death rate could be as high as .025% (1 in 5,000 patients which means most docs will never see a death so it will look safe). These are estimates and will be refined as I get more data. For example in one practice of 600 vaccinated patients, 6 have severe adverse events (SAEs) and one of those is near death. I can’t identify the physician because he is afraid of retribution. For 900 patients of Dr. Hoffe, 3 are permanently disabled and 1 died. Dr. Hoffe wasn’t afraid to speak out but telling the truth resulted in him losing his hospital privileges and having his reports torn up. Ask yourself, why would any doctor jeopardize their livelihood? He isn’t an anti-VAXer; he was pro-vaccination. He vaccinated 900 patients. He felt compelled to write up his serious concerns, basically “I have been quite alarmed at the high rate of serious side-effects from this novel treatment.” If the vaccine is as safe as they claim, you never see notes like that. Nobody has the time.
- It must be emphasised, that these people were not sick people, being treated for some
devastating disease. These were previously healthy people, who were offered an
experimental therapy, with unknown long-term side-effects, to protect them against an
illness that has the same mortality rate as the flu. Sadly, their lives have now been
- It is normally considered a fundamental principal of medical ethics, to discontinue a
clinical trial if significant harm is demonstrated from the treatment under investigation.
- So my last question is this; Is it medically ethical to continue this vaccine rollout, in
view of the severity of these life altering side-effects, after just the first shot? In
Lytton, BC, we have an incidence of 1 in 225 of severe life altering side-effects, from this
experimental gene modification therapy
This is why doctors will not speak out. Fear of retribution. There is no benefit to speaking up.
A superior alternative to vaccination is simply to treat a COVID infection with a proven early treatment protocol and to modernize our hospital protocols (which we are afraid to change to adopt drugs like cyproheptadine). This alternative results in significantly lower disability and death compared to the vaccines. Newer vaccines available soon appear to be much safer than the current vaccines.
Summary of key points covered in this document
- Vaccines are never supposed to kill people. The influenza vaccine doesn’t kill anyone. Zero. People die just coincidentally with the vaccination not from the vaccination, e.g., less than 1 person in the age group 30-39 dies per year according to VAERS.
- The COVID vaccines are unique in that healthy people who take the vaccine can end up dead or disabled at a rate that may be far greater than we have been led to believe. I will debate anyone on this publicly and they will lose.
- This vaccine is much more dangerous than any vaccine in our history. There are more reactions to this vaccine than all 70 vaccines in the last 30 years combined.
- We are essentially creating a nation of vaccine long-haulers. Some will be asymptomatic, some will have mild symptoms, some will have disabling symptoms, and some will die. The symptoms are all over the map
- At a minimum, if the FDA doesn’t halt vaccinations, they should require a BLACK BOX warning notifying people that the vaccine can kill you or cause permanent disability and the rates of both are unknown at this time. At least that way, people are going into this with their eyes wide open.
- The side effects of the vaccine can be both subtle and incredibly diverse because the vaccine can affect any part of your body, including your brain. For example, my fingers have now started to shake uncontrollably 2 months after my second dose. This sort of neurological damage is impossible to show cause and effect. I never would have ascribed it to the vaccine because I was told the vaccine was safe. But if they had told me that the vaccine causes my body to make a toxin everywhere, including my brain, any new neurological symptom within 3 months after any shot is highly suspect. I cannot report it in V-SAFE since you can’t make a proactive report. I will report in VAERS. Once you realize most people would never think to associate it with the vaccine because it happened 2 months later and the vaccine is supposed to be safe AND because most people don’t know about VAERS AND because most people wouldn’t bother to report it in VAERS since they would deem it too speculative, all this data is lost. V-SAFE never warned me that the symptoms can be subtle, diverse, and to report EVERYTHING that is NEW and ABNORMAL in VAERS. This is why the FDA and CDC isn’t seeing a safety signal. Had I not written (or read this article), I would have ascribed it to old age/bad luck. I now know better.
- We don’t know how many people this vaccine has killed or disabled. There is no transparency of these numbers and no analysis of the people who have died or been disabled. Of course we know these vaccines cause massive mini blood clots, so nothing is surprising.
- If you have anything happen to you within 3 months of either dose that is new and affecting your daily life, please report it in VAERS.
- We are collecting information from doctors. One doctor, with 600 vaccinated patients, reported that 6 of them had serious adverse events (requiring a hospital visit or hospitalization); 1 of those patients may die soon. This is very troubling. We don’t know if this is typical or not.
- Doctors are reporting adverse events in recently vaccinated patients that are off the charts. The range of conditions is unprecedented and doctors are baffled as to the cause and proper treatments. One 16 year old couldn’t speak or see just 48 hours after getting the shot. We don’t know how common this is, but even hearing a single event like this is extremely troubling. The press didn’t report it; I saw it in an email. So there must be dozens or hundreds of cases just like these that we are “unaware” of because it isn’t considered a vaccine-related event.
- The CDC admits that dozens of teenagers have been diagnosed with heart issues shortly after receiving the shot. Fear not! They are investigating, but they will not stop the vaccination program while they investigate. It’s been 2 weeks and no word.
- Normally, vaccination injects or generates a harmless antigen in your shoulder to generate immunity. It stays in your shoulder. These vaccines are different. The mRNA vaccines deliver instructions to cells all over your body to make a pathogenic spike protein over the next 48 hours: inside your brain, heart, ovaries, etc. The spike proteins damage your blood vessel walls and cause clotting. The spikes can break free of the cell membrane and freely circulate causing even more damage. The spike proteins can last around 30 days. The damage that has been done in the 30 days can last a lifetime.
- This is the reason people have a wide range of side effects: inability to see, inability to speak, heart attacks, myocarditis, pericarditis, bell’s palsy (half of your face doesn’t move), numbness in various body part, re-activation of shingles, etc. Some events are such as the teenager who killed himself after getting the shot are very hard to ascribe.
- A large fraction of the spike protein ends up in the ovaries (see nice line graph later in this article… it will shock you). We don’t know how the reproductive system of women will be impacted; we won’t know that for another 4 months. Nobody needs the jab that bad. Why not wait and see what happens?
- Social media companies do not want anyone to discover the problems until it is too late. Facebook for example has removed multiple “Vaccine side effects” groups comprising hundreds of thousands of users. If there are really no side effects, then what are these groups talking about? The weather? We don’t know because Facebook doesn’t want us to know. Don’t you love the transparency?
- Doctors are being told not to speak out or face the consequences. They are told not to associate deaths with the vaccine. Why is this needed if the vaccine is as safe as they led us to believe?
- We are not told about the alternatives including safer vaccines or refusing vaccination and if infected, treating with an early treatment protocol.
- Early treatment protocols with repurposed drugs are extremely safe and effective. If started within 48 hours of first symptoms, the hospitalization, fatality, and long-haul COVID rates are extremely low. In short, early treatment turns COVID into a mild cold.
- The NIH is deliberately sandbagging the approval of drugs used for early treatment and that sandbagging continues to the present. They know the drugs work, but they don’t want anyone to know. The guy leading the vaccine effort (Fauci) is the same guy suppressing the approval of alternatives because Cliff Lane, head of the Guidelines Committee reports to Fauci.
- If the government really wants to reduce vaccine hesitancy, they should make the rate of death and disability public rather than hiding these numbers. They are hiding this information from everyone including doctors on the weekly CDC calls. I asked one of them recently, “How many people has the vaccine killed so far?” He said “about 100.” There is no way just 100 people have died from this vaccine, I guarantee it. But it just shows you how they are hiding the true numbers.
- Tony Fauci and Cliff Lane should be removed from office. Their failure to deploy the Precautionary Principle of medicine and use all the available evidence has led to the needless loss of life of millions of people.
- The mainstream media and social networks have blindly followed the “authorities” and have contributed to the problem by enabling their false narratives and shutting out the voices of those who have legitimate challenges to these authorities.
- If you can prove the NIH got it right on ivermectin and fluvoxamine (they rated them NEUTRAL), there is a $2M reward waiting for you. Nobody has been able to do that because it is impossible. It is like proving that a baseball team with a 30-0 win loss record is a losing team. This is outrageous that Congress is so asleep at the wheel that they have not taken immediate action to direct the NIH to fix the Guidelines to minimize loss of life.
- Once you get vaccinated, you can never be unvaccinated. The damage may not be undoable and may only manifest itself years or decades later. It’s a bit like starting a small fire inside all of your key organs and letting it burn for 30 days.
- If I knew what I know now, I would not have chosen vaccination with the current vaccines for myself or my family. I would have waited for one of the newer vaccines which are not expected to suffer from these safety issues (but let’s see what happens). If I was at risk for COVID, I would prophylax with ivermectin. If I got COVID in the meantime, I would treat immediately with a 4 drug combo of fluvoxamine (50mg BIDx14d), ivermectin (12mg x 7d), simvastatin (….), and maraviroc (…) . This is what Dr. Bruce Patterson recommends to his patients and was developed from what has worked to cure long-haul COVID cases. If started within 48 hours of first symptoms, this protocol should be extremely effective because each drug targets a different mechanism of harm.
- If I already had COVID, I’d wait for the newer vaccines which confer broader immunity. Since I already have natural immunity in the meantime, there is no rush to vaccinate with a potentially unsafe vaccine.
- If you MUST get vaccinated now for some reason, take 50mg once a day of fluvoxamine starting 3 days before and continuing for 2 weeks. This will reduce inflammation and damage just like it does for COVID patients.
- These vaccines were rushed to market and they made a few bad design decisions. There is a way to re-formulate the current vaccines to significantly reduce the risk. If Pfizer or Moderna want to talk, you know where to find me. If the FDA expedites the fix, it could be fixed in as little as 60 days. I know of no reason they would not want to at least hear me out.
- Don’t you find it a bit odd that the CDC is telling kids to get vaccinated without showing proof that they are better off with the defective vaccine vs. taking their chances with the virus? I commissioned some experts to find out which was better and they threw up their hands because there is no data available to make the calculation because all the vaccine data is so bad (VAERS reporting). Their best guess is it was a wash. If you factor in an early treatment protocol if you get sick, then it isn’t a close call: just say no and if you get infected and then treat it early. And I challenge the CDC to show the actual numbers to prove I’m wrong (I’m happy to be wrong by the way… it does happen on occasion).
- Finally, not everyone will agree with me. I wouldn’t have gone through the trouble to write all this if I didn’t believe it was all true. I could be wrong. The FDA isn’t seeing a safety signal. But the FDA isn’t known for going out and talking to people in the real world and collecting data that way. They rely on official sources that can be grossly under-reporting the side effects in order not to scare anyone from taking the vaccine. I’m not making this up; there are lots of doctors that would vouch for what I’m saying. Check out Robert Malone’s article, for example where he refers to this censorship of evidence as “alarming.” So I’m not worried that the FDA sees different data than I do.
- Right now, the mechanisms of action point to putting your body at much greater risk than a natural COVID infection would cause. The natural COVID infection travels slowly through your body; the vaccine takes about 15 minutes to set fire to every part of your body at the same time (and the biggest fire is in your ovaries). This is why, when you do have a side effect from the vaccine, it can happen anywhere. You never see that with a natural infection. You get immunity either way. Some think natural immunity is broader and more durable, others disagree. But I think we are splitting hairs at this point.
- Lastly, let me address the elephant in the room. Some people have told me not to write this article. They believe that the upside of herd immunity and returning to normal outweighs the damage that is inflicted by the vaccine (which they believe is 100 deaths and no disabilities). I have several reasons for not agreeing: 1) the evidence on the table is all consistent with the hypothesis of a very destructive vaccine that has devastated a LOT of people, 2) they can fix the product quickly if they prioritize it, 3) if they kick Fauci and Lane out and replace them with reasonable people (in the mold of Michael J Ryan), we can get the drugs we need put on the NIH recommended list so if anyone does get COVID, it will be short lived and mild, and 4) this vaccine has the potential to wreak havoc on the reproductive system of our kids; if they can’t even tell us how many people have died and been disabled from the vaccine so far, I have little faith in their ability to project 9 months or more in the future. We know the toxic S1 subunit accumulates in the ovaries (see chart below; search for “Still Unconvinced”). Prove to me this isn’t a problem because it looks like it could well be a major train wreck to me. There is simply no way that after dozens of healthy kids have reported myocarditis and pericarditis (still unexplained by the CDC) that this vaccine could be anywhere close to safe. Nothing happens on a flu shot. This is off the charts and the dozens of kids affected is just the tip of the iceberg and this is just one of hundreds of symptoms caused by the vaccine. What the CDC observed in those kids is perfectly consistent with the narrative I outline here. In short, my explanation of what is happening here, and my assertion that the vaccine is causing harm to healthy people, matches reality. Their narrative (“it is perfectly safe”) does not. So, sorry, I’m not buying it. And I’m hardly alone in this belief:
If you believe everything I wrote above (or a trusted friend told you this is on the level), you can stop reading here.
Since there is a lot of misinformation on the Internet, let me give you a few tips to help you decide whether this article is on the level or not:
- Start with this site, Canada Health Alliance and watch their excellent 20 minute video. Bravo to them for pointing all that information out.
- Then read the superb petition to the FDA to revoke the EUA for the vaccines filed by Children’s Health Defense. Key excerpts in the next section.
- Listen to Dr. Bridle present the results of his FOIA request showing the vaccine instructs cells all over your body to create a toxin for 48 hours.
- My wife and I were the recipients of a National Caring Award. Evil people disseminating misleading information typically don’t get such awards.
- There are lots of stories about my philanthropy. Recently I donated $1.5M to the Glaucoma Research Foundation, for example.
- Look at the entire history of my Twitter posts. It would be hard to find any misinformation in any post. If there is, I’m happy to delete it. So I’m not a spreader of misinformation.
- I will appear on a “podcast” of a very famous personality who will have his channel cancelled if this isn’t true. His future is shot if this is misinformation.
- You can verify all of this with the inventor of mRNA, Robert Malone. He’s horrified about what has happened here; the muzzling of doctors, the lack of proper testing, the refusal to halt the drug when legitimate safety concerns have been raised, and the lack of transparency.
- The comments to date (June 4, 2021) have all been positive. That doesn’t happen when you spread misinformation. You are usually called out instantly.
- You can check me out with known, credible people like the Dean of the Emory School of Medicine Vikas Sukhatme, Peter McCullough, George Fareed and Brian Tyson, Dr. Joon Yun, etc. But this isn’t about me. This should be about the facts and I’m happy to debate anyone from NIH, CDC, FDA, Pfizer, Moderna, Merck, etc. to challenge me on any of this, but they will not show up at a fair debate. We can even host it live on CNN to make it more interesting. Similarly, what Dean of any US Medical School will debate me? None. Because they can’t use facts to discredit me because I’m telling the truth.
- I challenge anyone from the CDC, FDA, NIH, or WHO to debate me live. Nobody will take the challenge because they will lose. Badly. The CDC won’t be able to answer my simple questions. TrialSiteNews verified this independently because they did the debate “ask.” The NIH turned them down instantly with no reason. The WHO didn’t even respond. What are they so afraid of? Isn’t this America where the free exchange of ideas is embraced? Or do we want America to like China where there is a narrative from the government and everyone must follow the narrative without asking questions. It seems like we are moving to the latter.
- If Cliff Lane wants to debate me live, I will expose the corruption live and he will be unable to defend himself because there were a lot of people who also received the email I sent him.
- The Gates Foundation knows I’m not kidding about ivermectin and fluvoxamine working. They will not deny it. If they did, their credibility would be toast.
- The Fareed and Tyson protocol works and can be verified by hospitalization records independently. Early treatment works and the NIH just doesn’t want you to know that so they make it out like the drugs do nothing by giving them a NEUTRAL rating which has cost countless lives to be lost unnecessarily.
- A lot of people told me never to talk to them again after I wrote this article. Virtually all of them are “academics” whose reputations are at stake. If they speak out against me, they will hurt their credibility in the future as sooner or later the truth will come out.
- This whole thing didn’t exist until I was on a chance meeting with the Canadian Covid Care Alliance, a group of Canadian doctors who are appalled by what has happened to their profession. If you go on their website, you can get a two page summary of what Dr. Bryram Bridle presented at that meeting. If you register on that site, you will be sent Dr. Bridle’s full 20 page report (lay version for parents in about a week from now); the longer version for scientists is being written now (estimated to be in another week). The CCCA members and Dr. Bridle will debate anyone in the world on the merits of what is presented in Byram’s reports.
- After Dr. Bridle presented his results on a popular podcast, someone went to extraordinary lengths to try to discredit him through misinformation via a website and twitter handle. The perpetrator will not reveal his identity and refused my request to debate in an open forum. They like to hide in the shadows. If you want to challenge the doc, show yourself. They are not afraid to debate you, why are you so afraid to debate them?
- Mainstream media won’t air this because it goes against their narrative that the vaccine is safe and you should get vaccinated. If they give this story any airtime, it will hurt their credibility for not checking out the facts before promoting the vaccine to the public. If they refuse to give this story airtime, they will be digging themselves even deeper into a hole by compounding their mistake and continuing to promote a false narrative. They should let people know that people can die and be disabled from this vaccine. It is nowhere near as safe as the influenza vaccine, which is given out to the same % of people in the US without any reports of death or disablement. I bet you’ve never heard of anyone dying or being disabled from the influenza vaccine. But ask around and I’m sure you’ll find a lot of people close to you with vaccine horror stories either in your family or your friends.
- Early on in this pandemic it was me who was the truth teller saying we have to focus on using repurposed drugs as the fastest, cheapest, and safest way to turn COVID into a “mild cold.” I was right. If you start treatment early enough (ideally within 24 hours of first symptoms or discover earlier via PCR) COVID becomes a very minor cold that ends in about 3 days.
- I was right then about the critical importance of repurposed drugs, but it took the NIH over a year to acknowledge that. I’m absolutely confident that I’m right again. And it’s important that you believe me ASAP because while it is too late for me and many of you, the health of your kids is now at stake. I burned a lot of bridges by publishing this article. If I’m wrong nobody will believe me ever again. Why would I trash my credibility? The reason I can be so confident is simple: everything is 100% consistent with what I wrote here: the mechanisms of action are known, the toxicity of the spike protein and the free S1 subunit cannot be denied as it is in the published literature and measured in vaccinated people, the anecdotal stories from my friends, doctors, and others, the fact that other top people are speaking out, the fact that vaccine victims are damaged in a similar way as COVID long-haulers (Dr. Bruce Patterson and Dr. Ram Yogendra).
- I don’t believe the people running the CDC or FDA are evil. I think they are absolutely fine people who are simply relying on broken systems for safety signals. The FDA knows it cut corners in approving the drug for EUA without the appropriate toxicology studies. They knew about the biodistribution data. But they just believed the spike protein and the S1 subunit were “harmless” and they never expected that the S1 subunit would break off and become freely circulating. And even today, they think there is no problem because their systems aren’t detecting a problem. They should be spending a lot more time talking to doctors with lots of patients. If they reached out, they’d be horrified by the stories just like I was. They should talk to my carpet cleaner, Tim Damroth and his wife both of whom were disabled from the vaccine. If the vaccine only disables 1 in a million, then I just saw an event that could never happen. Reality eventually wins over the “narrative.”
This is reality. I captured this before Facebook could take it down. Here’s the link to the post. If the link doesn’t work, you can see what Facebook is removing from sight as “misinformation.” If the link does work, then even Facebook censors believe it is legitimate. There were 600 likes and 488 comments. Read all the comments. Those comments are the reality of what people are really thinking; it’s the narrative they don’t want anyone to have. There is no doubt this is vaccine related. It wasn’t 60 seconds before he took the vaccine… it was 60 seconds after. And the docs don’t know if it is vaccine related. This is why the CDC isn’t taking action because this is just a coincidence. Got it?
Ask yourself if the vaccine is so safe, then why does Facebook keep removing “Vaccine side effects” groups? Facebook employees are enabling this censorship to happen by not organizing and demanding that their company stop silencing innocent vaccine victims. Since when is it OK to censor facts and truth and civil discussion??
Marc Zuckerberg has no comment on this (he has a lot of money tied up in the vaccine and promised Tony Fauci to remove any content that goes against the false NIH narrative which is probably why when I tried to notify my friends that I’d be on 60 Minutes, Facebook censored my post). Does he support this or not? You have to take a side. This is preposterous and outrageous. Censoring victims of a dangerous vaccine is not in the public interest.
We are literally silencing free speech and nobody in Congress is speaking out about it since it goes against the narrative that the vaccine is safe. Some leaders in Congress will emerge sooner or later. Who will be first to demand the actual names of people who have been killed or disabled so that we can see how much under-reporting is happening? Ask yourself, if this vaccine were as safe as the influenza vaccine, these posts would be rare to non-existent.
Here’s an email from an ER doc showing why these events can be difficult to attribute to the vaccine. This is why surveying primary care docs is more useful (and asking the % of severe adverse reactions in their vaccinated patients). Ask yourself these two questions: 1. if the doc thought these events were normal, why did he bother to draft the email at all and 2. why is he afraid of retribution for speaking out about what happened? Note the frank comment about the event reports… there is no reward for filling these out and they are a time suck that nobody wants to do. So most of the events don’t get reported. This is why the CDC and FDA never see a “safety signal.”
Some anecdotes for you:
xxxxx Hospital in xxx where I work, has 2 cases of Guillain-Barre syndrome currently admitted. Both developed within 2-3 days of first vaccine, one in a 40yr old, the other in a 50yr old.
We had a 64 year old female smoker die of a massive PE 5-6 days after vaccine. I know for a fact this was not reported as a possible vaccine event, even though I told the physicians I think they should report it.
We have had at least 2 DVT’s within a short time after vaccine.
A girl in her 20’s with a clotting disorder permanently on Fragmin because of previous PE had another PE after vaccine, but had also been non-compliant with Firagmn for 48 hours, so unclear.
I had a lady admitted to me with “sepsis” when I was on the hospitalist service, 16 hours after vaccine. Workup negative for any other cause.
I have personally seen three cases of “COVID arm”. Not until the third did I figure out this is not cellulitis and doesn’t need antibiotic treatment.
I am hearing issues from further afield.
This is such a tough issue to sort out statistically because, with the majority of the public being vaccinated, most of these issues are probably unrelated to the vaccine and statistically predictable without it. But having filled out the adverse event form, it is obviously a massive barrier to reporting – 5 pages of blanks and checkboxes. I know at least 2 docs who said “F— it” once they saw the form.
Email from a doctor who requested his name be withheld for fear of retribution
I just received this text:
If you’re still not convinced, or just want to learn more about how the vaccine really works and how you were misled, the rest of this document is to prove to you that everything I’ve said above is accurate and it goes into a lot of detail. That’s why it is so long. It’s a lot to cover when you are up against a false narrative of this magnitude. And this is a work in progress to finish it up and clean it up. But I thought it was important to get this out so people can think it over and make their own informed choice as to what to do.
If you’d like to help me clean this doc up and you have a passion for the mission and enough medical knowledge to understand it all, DM me on Twitter @stkirsch.
I always get vaccinated. I have been fully vaccinated with the Moderna vaccine.
However, based on what I now know about the vaccine side effects, current COVID rates, and the success rate of early treatment protocols, the answer I would give today to anyone asking me for advice as to whether to take any of the current vaccines would be, “Just say no.”
The current vaccines are particularly contraindicated if you have already been infected with COVID or are under age 20. For these people, I would say “NO! NO! NO!”
In this article, I will explain the reasons why I have come to this conclusion. You will learn how these vaccines work and the key mistakes that were made. You will understand why there are so many side effects and why these are so varied and why they almost all happen within 30 days of vaccination. You will understand why kids are having heart attacks, losing their sight, and ability to talk.
This was written on June 1, 2021. My views may change as new evidence and new vaccines emerge. I’m particularly excited about the Novavax, Covaxin, and Valneva vaccines because they may have a superior safety profile than the current vaccines and the Valneva is likely to lead to much broader immunity.
First, here are a few things I want you to know:
- The views in this article are not shared by most mainstream scientists who insist that the current vaccine is the best choice for everyone.
- The arguments are very polarizing: each side insists they are right and the other side is completely irresponsible and unethical.
- As proof of #2: I firmly believe that the mainstream scientists have got it completely wrong and clinicians with over 500 patients have it right.
- There is absolutely no question that vaccination with the current vaccines has a risk of adverse effects. They are much riskier than traditional vaccines. For example for age range 30-39, there have been just 7 deaths in the past 10 years (2010 to 2019) reported in VAERS for the influenza vaccine compared to 68 deaths from the COVID vaccines in 2021 alone (ending in May 2021). Watch this video which explains the process I used to get the 100X. This suggests the death rate is more than 100 times greater for this vaccine compared to the influenza vaccine (the influenza vaccine doesn’t kill anyone statistically; these are just background deaths since people die all the time). This means this vaccine is not safe; it is killing people.
- Based on what I know today about the serious adverse events (SAEs) and death rates, choosing not to vaccinate (and if you then later get COVID, treating it early) is the superior option. This is especially true for those under age 30; the risks of infection are lower and the early treatment protocols are more effective and proven.
- I have an ethical obligation to report that option to people because I believe it will save lives and avoid debilitating serious adverse events caused by the current vaccines many of which may be permanent.
- Over 4,200 COVID vaccine related deaths have been reported in the VAERS system. Nobody knows the exact number, but it is likely much higher since VAERS is a voluntary system and I know that doctors are being discouraged from reporting vaccine related deaths. Conversely, had the 600K people who had already died from COVID infections been treated early, the number of deaths to date could be reasonably estimated to be significantly less than that. For example 6,000 patients if not treated would produce at least 300 hospitalizations (since average age was 60). Early treatment with a proven protocol (such as that of Fareed and Tyson) has been shown to reduce that to 1 hospitalization with the same cohort. These are actual numbers in real life in multiple independent practices. This is a 300x improvement. Therefore, a rough estimate is that only around 2,000 people would have died if we had told people to treat the virus early with an effective protocol and we had 100% compliance. If we add a prophylaxis protocol (such as with ivermectin), we reduce the deaths even more to around 400 dead. This means there is likely more than an order of magnitude difference between the options in favor of do not vaccinate.
- By using modern hospital treatments such as cyproheptadine, leronlimab, inhaled adenosine, and the ExThera Seraph 100, even if someone is hospitalized, we can reduce the chance of them dying by up to a factor of 4 or more, leading to <100 people dead in the US, all without the need for vaccination just by allowing doctors to use the best evidence-based treatments on the table.
- Had the CDC told people to treat the virus early with an appropriate protocol, we would have never had a pandemic since this would result in a fatality rate that is around two order of magnitude lower than the number of people killed by the flu in a typical year. Early treatment also avoids the huge amounts of vaccine SAEs many of which are debilitating. And it reduces the risk of damage to brain, heart, and reproductive tissues. We know that the vaccine is delivering spike protein to these areas; that is not longer debatable. I think the big mistake was keeping quiet about the value of early treatment and only talking about the vaccine as the only option.
- Front line doctors who are actively treating patients have a different view than the CDC. For example, a group of doctors I know have shifted from 100% pro vaccine to 100% against the current vaccines based on their own personal experiences (wide range of rare, inexplicable serious conditions).
- Highly respected physicians such as Peter McCullough who previously thought the vaccine was safe have now realized they made a mistake and are now publicly telling people not to vaccinate.
- A doctor I know has 1,200 total patients of which 700 are vaccinated patients. He has 15 patients with severe adverse reactions including heart attack, congestive heart failure, acute pancreatitis, with one “now near death.” A serious event rate of 1 in 50 is totally unacceptable; it’s almost as bad as the virus itself. It’s likely less than that on average, for example, I know another frontline doctor who has 550 patients; 90% have been vaccinated and there were no significant lasting adverse events. Why aren’t we getting the actual data from the authorities? I am having to resort to data collection myself directly from physicians to find out the serious event rates since this is not being disclosed. Really? We expect everyone to do this?
- The fact that there were Facebook “Vaccine side effect” groups with over 200,000 members before Facebook censored them is objective evidence supporting the clinicians.
- I believe the current vaccines can cause very debilitating side effects and could be fixed so that they are a lot safer than they are today (by removing the PEG, decreasing the dosing, pre- and post-medicating).
- I am PRO-VAX. I think vaccinations in general are fabulous. I have always gotten vaccinated in the past. I got the Moderna vaccine in March 2021. Both doses. The mRNA vaccines are fabulous in general. But NOT when the antigen is problematic and you include PEG so it gets broad distribution. That’s the issue: the s1 subunit antigen combined with the PEG in the vaccine means that a pathogenic antigen (s1 subunit) is now being manufactured (for up to 48 hours before the mRNA falls apart) in all parts of my body including inside my brain and causing blood clots and inflammation for up to around 30 days until almost all of those cells either are dead or destroyed. For more detail as to the cause of the clotting and bleeding, listen to this excellent 10-minute interview of Byram Bridle.
- My issues are SOLEY with the SAFETY of the CURRENT vaccines as compared to the efficacy and safety of outpatient prophylaxis and treatment protocols. The number of significant adverse reactions is abnormally high and it isn’t clear if these are reversible. The lack of transparency and censorship are both troubling.
- Knowing what I now know, I would not have made the same choice if given the option today.
- I would not allow my kids to be vaccinated with the current vaccines. The risk-benefit tradeoff doesn’t justify it.
- I have insider knowledge of the safety and efficacy evidence of early treatments that few people have which gives me a unique perspective that few other people in the world have. I also have insider knowledge of why the establishment is improperly rejecting these treatments and pretending they don’t work. I believe that early treatments are superior to the current vaccines in terms of minimizing death and disability.
- My sole objective in writing this is to minimize the number of people who end up dead and/or permanently disabled
- The CDC has not made a compelling case that vaccination is better. That’s because they can’t as you’ll see in the next section (Children’s Health Defense filing).
- If I previously had COVID, I would not get the vaccine due to the risk of adverse reactions risk.
Here is an example that makes it crystal clear that refusing vaccination saves lives.
Children’s Heath Defense Petition to FDA to revoke EUA on COVID vaccines
Here is the full petition.
Here are a few of the most relevant sections:
- FDA should immediately amend its existing guidance for the use of the chloroquine
drugs, ivermectin, and any other drugs demonstrated to be safe and effective against COVID, to
comport with current scientific evidence of safety and efficacy at currently used doses and
immediately issue notifications to all stakeholders of this change.
- The FDA should issue guidance to all stakeholders in digital and written formats to
affirm that all citizens have the option to accept or refuse administration of investigational COVID
vaccines without adverse work, educational or other non-health related consequences, under 21
U.S.C. § 360bbb-3(e)(1)(a)(ii)(III) 1 and the informed consent requirements of the Nuremberg
- Pending revocation of COVID vaccine EUAs, FDA should issue guidance that all
marketing and promotion of COVID vaccines must refrain from labeling them “safe and
effective,” as such statements violate 21 U.S.C. § 360bbb-3.
- Finally, reflecting on the FDA’s regulatory history is helpful: A proven association
between the 1976–1977 swine influenza vaccine and approximately 400 cases of Guillain–Barré
syndrome halted that particular national vaccination campaign. The reported deaths following that swine flu vaccination campaign, 30 out of 40-45 million vaccinees, were insignificant compared to the current reported death toll of 4,434 due to COVID vaccines. Today’s death rate is more than 50 times higher than that which ended the swine flu vaccine campaign.
- Regarding the halted swine flu vaccine program, the CDC’s Emerging Infectious
Diseases Journal concluded, “In 1976, the federal government wisely opted to put protection of
the public first.” FDA should learn from this past experience and again put protection of the
public first. It is imperative that the FDA swiftly take action to authorize alternative treatments
- There are 74 million children in the United States. So far, 282 have died “involving
Covid.” Two hundred eighty-two in 74 million is a rate of 0.00038%. While many children may
not have been exposed to COVID, CDC estimated that 22.2 million children aged 5-17 had had
COVID and 127 had died, at the May 12, 2021 meeting of the Advisory Committee on
Immunization Practices, or 0.00057%. Available evidence strongly suggests that the vaccine is
much more dangerous to children than the disease.
- A recent opinion piece in the British Medical Journal noted that “the likelihood of
severe outcomes or death associated with COVID-19 infection is very low for children,
undermining the appropriateness of an emergency use authorization for child covid-19 vaccines.”
The authors also suggested child vaccinations could strategically harm vaccination efforts and
increase vaccine hesitancy.
Here are some more headlines that challenge the notion that “everyone should vaccinate including kids”:
A good friend of mine is a doctor in Canada. Of the 600 patients who got the jab, 15 have SAEs. 5 of those are hospitalized. One of the hospitalized patients is near death. This same doctor in 29 years has never had any SAE from the flu vaccine. How do you explain this?
Write-up: Patient’s niece reported that the patient’s arm became sore, had stomach upset, fever the day after the vaccine. The following day the patient died. (24 hours after being vaccinated)
16 year old girl cannot talk or see 48 hours after vaccination.
More than 25% of all adverse events ever reported over the past 30 years from all vaccines are from the COVID vaccines which makes COVID vaccines the single most destructive vaccines in human history.
The New York Times (May 22, 2021): CDC Is Investigating a Heart Problem in a Few Young Vaccine Recipient. They will not say the number but it is more than a few. Teenagers never have heart issues after a vaccination. The article itself says “several dozen reports” of myocarditis yet the agency says relatively few cases (relative to the 100M vaccinated presumably) so as not to panic the public.
Here is a letter to clinicians in Maryland showing that this is not normal.
Shingles and herpes zoster infections are known to be re-activated by the vaccine. This was confirmed by an insider at the FDA who used computer analytics to see the association.
Under reported examples
Some examples of under-reporting:
- Dr. Hoffe’s reports were all removed.
- Had an ivermectin consultation with 2 seniors who don’t want the vaccine; their daughter a school principal took first dose of Pfizer; almost immediately suffered severe undiadnosable neurologic symptoms; numbness; been to ER x 3; saw neurologist; was questioned whether it’s in her head; NO ONE CONSIDERED THE VACCINE AS THE CAUSE. I told the mother that her daughter’s problem is likely spike protein disease and is real and must be reported. I sent her the forms to give to the family doctor; provided the correct fax number. I insisted these events MUST be reported. It has been 5 weeks and she is slowly improving. I warned that Public Health will tell her to take the second dose (which she will not).
- … you get the idea… physicians pressured to not blame vaccine or just unaware of the range of symptoms or form too long, etc.
Why are the current COVID vaccines so dangerous
Listen to this excellent 10-minute interview of Byram Bridle for detail, but basically:
- PEG enables the lipid nanoparticles to invade the entire body including crossing blood brain barrier. They don’t just stay inside your shoulder.
- The mRNA fuses into cells and instructs them to produce the spike protein
- The spike protein is not benign as had been assumed. It will attach to the ACE2 receptor in platelets causing them to clump which leads to clotting. It will also attach to blood vessel walls (ACE2 receptors on endothelial cells) causing bleeding. All this damage in turn, creates inflammation which makes things even worse. The blood clots and bleeding cause all sorts of disorders (blindness, inability to speak, numbness, etc) depending on where they are.
- The biodistribution safety studies were not done with the actual vaccine (a big no-no). But they showed distribution all over the body, including brain, ovaries, adrenal glands, etc. This will be published in Byram Bridle’s next summary. See Fig below.
- What’s even worse is that the dangerous S1 subunit protein doesn’t remain bound to the cell, but can break off and becomes freely circulating (aka free s1 subunit spike protein) as these Harvard researchers measured in vaccinated patients. This increases the damage potential significantly because if the original distribution (from the LNP) was limited in key organs, the free spike is able to reach many more areas. The analogy is delivering a small box of pathogen to the front door of each house in a neighborhood. When you open up the box, instead of the pathogen being expressed on the outside of the house, the pathogen breaks off and is now free to engulf the entire neighborhood (and surrounding neighborhoods) in pathogen (s1 subunit).
- This free S1 protein may be transferred via breast milk to infants which then can wreak the same havoc on the child’s body. This is a hypothesis but it would not be surprising to have the spike protein in the breast milk of some lactating women if they were to be vaccinated. Proteins circulating in the blood usually get concentrated in breast milk. Notably, there have been some adverse events reported of infants experiencing bleeding in their gastrointestinal tracts after suckling from mothers who had received a COVID-19 vaccine. This hypothesis would explain it (and afaik is the most likely explanation; is there another?). Byram Bridle’s full paper (not yet available) will go into this further. Incorporating the spike protein into an infant’s immune system will teach the infant that the spike protein is “good” and should not be attacked in the future. This means that if infected in the future, the child may be unable to get rid of the virus, and would have a life-long susceptibility to the virus.
When you get vaccinated, you start generating the s1 protein inside all your organs. While accumulation outside the injection site is minimal, because it is generated everywhere, including inside your brain, it explains the huge range of side effects.
Therefore it comes as no surprise that people suffering from vaccine side effects have EXACTLY the same biomarker profiles as long-haulers according to the scientists at what I consider the world’s leading COVID long haul clinic. The vaccine is supposed to do no harm and simply prime your immune system. It is not doing this. It is causing damage. There is absolutely no question about that.
See the 2 page summary paper on canadiancovidcarealliance.org for a more detailed description..
So there were 3 major errors:
- not removing the PEG from the formulation which would have localized the distribution to the injection site more
- assuming the spike protein and s1 subunit were benign (which means the distribution profile is not harmless)
- assuming the s1 subunit would remain bound to the cells where the mRNA was delivered. This is not the case as s1 is seen circulating in the blood. This is very problematic: it means that even if you fixed #1, you could still be in trouble since this will likely affect all vaccines. The S1 subunit appears to be the most toxic part of the virus. This explains the wide range of symptoms people have after receiving the vaccine.
But wait… there’s more! Here’s one explanation for why you get free S1 subunits proposed by Stephanie Seneff (MIT):
But then I think maybe the most disturbing thing to me is they actually modified the code so that it doesn’t produce a normal version of the spike protein. It produces a version that has a couple of prolines in it side by side at the critical place where this spike protein normally would fuse with the cell that it’s infecting. So the spike protein binds to the ACE2 receptor once it’s produced by the human cell, according to the vaccine instructions. But it’s a modified version of the spike protein. It has these two prolines that make it very stiff so that it can’t reshape. Normally it would bind to the ACE2 receptor and then it would reshape and go straight into the membrane like a spear. And because of this redesign, it can’t do that so it sits there on the ACE2 receptor exposed.
And of course, this makes it much easier for the antibodies to be produced because I mean it can’t hide its underbelly because it’s been engineered to keep itself open.
Stephanie Seneff, private conversation June 2, 2021
I wrote to Malone to confirm this. He wrote back:
yes, it is locked into a pre-fusion confirmation.
It has a transmembrane anchor added which is supposed to keep it in the membrane of the cell that expresses it after mRNA transfection.
But clearly there is a proteolytic cleavage step that is happening (no surprise) which is cutting it free from the transfected cells.
We know it is being clipped because of the HMS/Brigham paper measuring free spike in the blood of vaccinees.
All of this should have been sorted out before it went into humans.
Email from Robert Malone, inventor of mRNA vaccines
Finally, for scientific readers, here’s more on the PEG usage (that is above my pay grade):
- The PEG is linked to a short acyl chain, and is there to stabilize the formulation prior to injection.
- The PEG disassociates from the lipoplex after injection
- Yes the synthetic ionizable cationic lipids are a key part of the formulation. They are what drives (thermodynamically) the coating of the polynucleotide and the overall self-assembly process.
- Both the PEG and the synthetic cationic lipids (that are added to the nanoparticles to make
them extremely immunogenic) can be removed. The delivery will not be as efficient, but naked RNA does work.
Is this true for other vaccines?
Yes. J&J is affected too. J&J has the same modified version of the spike protein.
Why is the CDC ignoring all these warning signals?
You’d expect that the CDC monitoring would have picked up the myocarditis in kids early and it worked: it did. But interestingly, the Israeli’s who are highly skilled at this and have a much more controlled health system did not. This is interesting because it shows these detection mechanisms can have flaws.
The CDC knew early about this, but as more case reports came in, they issued an advisory about 2 weeks ago.
These events are clearly vaccine related. The myocarditis and pericarditis always happen right after vaccination (within a few days). They are more common after the second dose. This tells you for certain that it is the vaccine that is causing these events; we didn’t just get “lucky.” If it were random, the first dose would be same rate as second dose.
Why isn’t the CDC halting the distribution of the vaccine to kids until the cause is determined so that the vaccine can be “fixed”? They aren’t.
If you ask Byram Bridle, he’ll tell you in seconds exactly why this happens; the narrative we just described fits all the observations.
However, the CDC remains completely baffled even though they have been “working on it” for weeks. I’m sure it will take a while before they do. They will simply remain baffled and just tell docs to treat it.
The reason for this is simple. Even though Bridle’s analysis explains everything, accepting Bridle’s analysis means that they would have to admit they approved a very unsafe vaccine. That would look bad. So better to keep saying “we are looking at it.”
If they are truly baffled, why not make the existing case reports public and reveal their current hypotheses so we can use the brainpower of everyone in the world to find the probable cause? This would be in everyone’s best interest.
In the interim, they should adopt Byram Bridle’s hypothesis since it PERFECTLY FITS ALL THE FACTS until they find a better explanation. That’s the safest thing to do. But finding a second perfect fit… that’s really really unlikely. Therefore, it is very likely Bridle got it right and using that in the interim is the safe thing to do to protect the public.
Why early treatments are so safe
Early treatment using repurposed drugs is the fastest, cheapest, and lowest cost way to end the pandemic. These drugs are safe, effective, and they have a well known safety profile. Ivermectin for example, is one of the safest drugs ever invented.
The earlier you start a protocol, the better. In Mexico, they start people on drugs even before the PCR test comes back. Their hospitals are empty. NEVER NEVER wait for symptoms before starting treatment if you can avoid it (a common mistake doctors make is to only treat if symptoms; but that can be too late for minimizing the impact).
Viruses are ALWAYS best treated early (just like a fire). Hit early and hard, just as David Ho advised with HIV.
Because Fauci didn’t prioritize outpatient treatment early on and made sure than no repurposed drug gets NIH approval no matter how convincing the evidence is even when nobody in the world can defend these recommendations. Otherwise, if proven he made a huge mistake that cost trillions of dollars and millions of lives, he’d look bad and lose his job.
Congress is still blind to Fauci. They think he walks on water. He doesn’t. When he was given inarguable proof these drugs worked, all we got back was silence. If Congress were to actually question him on this, his position is indefensible (see this article). Cliff Lane knows all the evidence-based medicine requirements for a FOR recommendation have been met.
If we had used early treatments and novel in-patient treatments (adenosine, cyproheptadine, etc; see the videos on TrialSiteNews), the death rate from this virus would be in the low thousands making it far less dangerous than influenza which can kill between 20,000 and 60,000 people a year.
Why you should never get vaccinated if you are immune already
If you’ve had COVID already, there is no quantifiable benefit to getting vaccinated. It’s also more dangerous.
If you are not sure, it is safest to always ScreenB4Vaccine to see if you might already be immune. If so, just say no.
Ranking the options
At the present time, if I had to order preferred approaches to COVID I would choose:
- Novavax, Covaxin, or Valneva vaccine when widely available if the superior safety data is confirmed (no free spike in blood, distribution limited to arm, no SAEs) and I haven’t had COVID
- Prophylaxis then early treatment if infected while waiting for #1
- Current vaccines using pre-treatment and post-treatment to address clotting, inflammation, endothelial cell damage but ONLY if I had to be vaccinated for purposes of business or travel or some other reason and #1 wasn’t available. 50mg fluvoxamine starting 3 days before continuing for 3 weeks after should minimize the damage.
It is important you speak with your doctor before making your decision so that you can make the decision that is right for you.
In normal times, this article wouldn’t need to exist: the best choice would be vaccination hands down.
However, today (May 30, 2021), the vaccination decision is much more complex for the following reasons:
- Lack of transparency as to the rate of serious adverse reactions (including death) associated with the current vaccines
- Deliberate censorship of side effect reporting (such as Facebook removing multiple “Vaccine side effect” groups of hundreds of thousands of people)
- Troubling anecdotal reports from my friends and from doctors I know
- Questions of vaccine safety have been raised publicly by respected scientists
- A large respected group of physicians who had previously recommended vaccination (and is now 100% against vaccination). I can’t name them for fear of retribution.
- One physician who regularly gives vaccines to his patients told me “in 29 years of practicing medicine, I’ve never seen anything like this.” He is afraid to speak out publicly for fear of retribution.
- No transparency as to the risk/benefit ratio for kids of the vaccine vs. getting COVID (which would require disclosure of the serious side effect rate of the vaccine).
Those are some of the reasons I am extremely concerned about the safety profile of the current vaccines.
For example, one could reasonably ask, if the vaccine is perfectly safe, then why aren’t the reports in the V-SAFE database available to the public? Why is there censorship of vaccine victim self-help groups? Why isn’t there a guideline for treating adverse events resulting from the vaccination?
Should we vaccinate our kids?
It is impossible to justify. Look at this table. It shows vaccination for kids could cause more harm (from vaccination) than lives saved. Only if we had a super safe vaccine with no adverse events would we ever consider this. We should never consider it until we actually have the vaccine side effect data in public view that would enable parents to make this decision.
Alternatives to vaccination
I’m all for vaccination but history has shown that developing a safe and effective vaccine takes years. The current vaccine fiasco rushing it to market will end up proving this once again. But the lessons learned in this pandemic may help us to do the next one faster.
If there was no alternative to vaccination today, then even with its flaws, vaccination with a “black box warning” vaccine may be preferable for many people.
But there are viable alternatives (that the NIH is deliberately suppressing) such as
- early treatment if infected (and advanced hospital treatment in the rare event you are hospitalized)
- waiting for the Novavax, Valneva, or Covaxin vaccine,
- pre- and post- medicating with the current vaccine.
The best choice for you depends on a number of factors including whether you’ve already had COVID, whether you need vaccination proof for work and/or travel, your risk factors, your age, the current chance you will get COVID in your community, and more. Not having public access to reliable adverse event data in order to make the best decision is troubling.
If you’ve already had COVID, you have natural immunity and if you want even higher protection, you may be better off waiting for a very safe vaccine.
If you are troubled by issues with the current vaccine, treating COVID early with drugs such as ivermectin and fluvoxamine, have been shown to be extremely effective with minimal (minor and temporary) side-effects.
If you believe the current vaccines are perfectly safe, consider adding aspirin and fluvoxamine both before and for 10 days after vaccination as a way to reduce inflammation in the presence of the spike protein.
The inventor of the mRNA vaccine wrote this post which brings up legitimate issues with requiring vaccination of an experimental vaccine. This article raises issues about how the vaccines were not properly tested (and still lack the required safety studies).
Please watch this video: Legendary Epidemiologist Sucharit Bhakdi on the Covid Vaccine.
Timeline: How did we get here
1) December 2020: Data looks good for COVID-19 naive adults getting vaccines to prevent mild COVID-19.
2) March 2021: at 1600 deaths. CDC and FDA fail to call for external data review panels. Odd.
3) April 2021: CDC reports 10K vaccine failures (vaccinated people got the virus)–could be 10 fold under reported
4) May 2021: CDC VAERS data indicate COVID vaccines have more safety events than all 70 vaccines combined all years in history.
So physicians were enthusiastic and recommended the vaccine early and have progressively become less optimistic with the catastrophic safety numbers. Vaccine centers started to decline in visitors April 8 and are now empty. CDC promoting lotteries of $1M for persons to consider gambling their lives with the vaccine. Likely the most disastrous vaccine campaign in human history.
Now that Americans are 50% vaccinated and most are adults fearful of COVID and seniors, we can lessen the intensity of the vaccine program and focus on treatment strategies for fewer COVID-19 cases both in the unvaccinated and vaccinated.
Questions to ask before taking the current COVID vaccines
By multiple measures, these vaccines are 100x more dangerous than previous vaccines. I’ve never personally heard of any adverse reactions from the influenza virus; from this vaccine, I hear them all the time.
The argument is that the benefit outweighs the risk, that you are 90% less likely to get COVID if you are vaccinated, and less likely to be sick if you do. Yet superior outcomes are regularly achieved with early treatment protocols, but without the risk profile. Where is the comparison of risk benefit vs. repurposed drugs? There isn’t one because the NIH and WHO have unjustifiably made it clear that people shouldn’t use these options despite compelling evidence.
As a result, Italy is planning to make the vaccine mandatory for all citizens.
If you live in a region of the world that still has free choice, here are some ideas for questions you may be interested in asking before you get the jab. The issue is you want to get informed consent with the emphasis on informed because today you give consent, but they aren’t telling you the risks which for these vaccines are significantly higher than typical vaccines:
- How many people in the US have died within 30 days of receiving this vaccine? Why is this not disclosed?
- How many people worldwide have been permanently disabled within 30 days of receiving this vaccine?
- How many people worldwide have been hospitalized within 30 days of receiving this vaccine?
- How does the side effect/safety profile of these vaccines compare with the Novavax, Valneva, or Covaxin vaccines (death, severe reactions, brain clots, heart problems, etc)?
- I’ve heard of very severe side effects from this vaccine. I know many people who are disabled and the doctors cannot help them. So isn’t it true that there are many severe side effects from this vaccine that can leave me disabled where the doctors have no idea on how to get me back to normal?
- If the s1 subunit that is generated all over my body after vaccination is so harmless, then how do you explain the wide range of bizarre neurological events reported AFTER people get the vaccine?
- What did the CDC determine was the cause of myocarditis in vaccinated teenagers? Shouldn’t we stop until we can determine the cause? How many cases were there and why wasn’t this disclosed?
- How does the death rate compare with the influenza vaccine?
- How does the rate of heart attacks compare with the influenza vaccine?
- How does the rate of myocarditis in teenagers compare with the influenza vaccine?
- How does the rate of brain clots compare with the influenza vaccine?
- How does the rate of disabling side effects compare with the influenza vaccine?
- If the vaccine is so safe, why did Facebook need to remove vaccine side effects groups totaling hundreds of thousands of members? What were they talking about?
- Why isn’t the V-SAFE database publicly searchable? There is no transparency. What are you trying to hide?
- If I have a disabling side effect, are there proven treatments that can reliably resolve them?
- If I do have a vaccine side effect, is there a self-help Internet discussion group left that isn’t being censored that I can join?
- Why weren’t the proper toxicology studies ever done that would show the amount of spike protein made in each part of my body? Shouldn’t these be done now in rhesus monkeys since they closely mimic the ACE2 binding affinities of humans?
- Why isn’t there an analysis of the over 5,000 deaths available publicly?
- Why would I ever want to allow my children to get this vaccine? They have low risk of getting COVID, very low risk of dying if they do get COVID, and with modern early treatments, and modern hospitalized patient treatments, it seems almost certain that they would have a greater chance of dying from the vaccine than from COVID.
- Why are the drug companies who are collecting the significant adverse event data allowed to keep this information private? Shouldn’t this be disclosed publicly? If this vaccine is as safe as we are told, there should be nothing to hide.
- We have never let pregnant women get injected with investigational biologically active substances, why would the CDC recommend the COVID-19 vaccine in pregnant women without many years of extensive safety testing?
- Since the dangerous spike protein circulates in the body for up to a month after mRNA vaccination, why would people be allowed to donate blood during those two weeks? Isn’t the blood supply now contaminated with SARS-CoV-2 spike protein? What are blood banks doing to test for spike protein and assure safety of the blood supply?
- Why do mRNA COVID vaccines go to the ovaries and testes and then increase tenfold over the next 48 hours after injection? Is that safe? Is that related to reported menstrual irregularities in women?
- Why does the investigational program not have a Clinical Event Committee, Data Safety Monitoring Board, and Human Ethics Committee like other big clinical investigations?
A look at the numbers
A lot of people tell me, vaccination may have side effects, but even with the side effects, it is better than getting COVID.
But this is not true if you knew that early treatment protocols can reduce death rates by more than a factor of 100. So it has a superior risk benefit ratio, especially with the current vaccines.
Fareed and Tyson have a near zero hospitalization rate with over 6,500 patients (avg age 60) so that’s over 300X reduction (assuming a 5% hospitalization rate, we’d expect 350 and got 1).
It’s sobering that on average you need to vaccinate around 100 people to prevent one case of COVID-19. This implies that symptoms due to the vaccine had better be only 1/100 as severe as symptoms due to the disease, just to break even. One severe reaction out of 100 is enough to turn the tide in favor of disease over vaccine. There is a big difference between the absolute risk reduction (ARR) and the relative risk reduction (RRR). Credit to Stephanie Seneff for the observation.
This vaccine fails to meet the 1 in 100 standard based on data I’m seeing from physicians. And it fails miserably compared to early treatment protocols.
Once we had a safe vaccine with no significant adverse side effects (e.g., perhaps like the Novavax, Valneva, Covaxin vaccines), then going for the peace of mind with those vaccines would be preferable. Valneva in particular should confer much broader immunity.
What I object to
There are three things that everyone should find very troubling.
- We are urging people with natural immunity to get vaccinated. This is wrong. This is an unnecessary medical procedure which is a violation of what physicians are taught. The reason doctors are recommending it is they don’t know how robust natural immunity is, so they are erroring on the side of caution. That would be fine if these vaccines were as safe as the influenza vaccine, but they aren’t. Hence the advice to everyone to get vaccinated is absolutely wrong. The side effect profile is much worse from these vaccines if you’ve already had COVID. So not only is this unnecessary (since natural immunity is showing to be both broad and robust), but it increases risk for no benefit.
- Patients are not giving informed consent. They are giving consent, without the informed. We are not informing them of the risks because if we did that, nobody would take the shot. For example, a top infectious disease doc I know sits on the weekly CDC briefings and I asked him, “how many people have died from the vaccine?” and he said “about 100.” So we aren’t informing the doctors since if they knew the numbers, they wouldn’t recommend the vaccine. This is why the V-SAFE database is kept from public view. It is not hard to find doctors with >1,000 patients will tell you that this vaccine’s side effects are off the charts, like my friend with 0 side effects over 29 years, now has 15 of 700 patients with significant adverse effects, 5 in the hospital, and 1 near death. Nobody knows this. Informed consent would include letting people know that there are other vaccines with significantly better safety profiles that should be available soon. Informed consent would include letting people know that there isn’t a study showing a clear benefit if you’ve already been vaccinated, and significantly higher risks than for people without natural immunity.
- Vaccination should not be required for travel and school. We shouldn’t force people to be vaccinated in order to do necessary activities when early treatments are extremely safe and effective. With early treatment, COVID infections can be less risky than getting the flu. We don’t require flu shots. The NIH is a huge impediment here by refusing to put early treatment on their guidelines.
I am not alone; even the inventor of mRNA vaccine is mortified
It’s not just me that thinks this vaccine is bad news. So does the inventor of the technology. See
“What was most alarming to me was that my clinical primary practice physician colleague told me that each of these cases were reported as per the proper channels in Canada, and each was summarily determined to not be vaccine related by the authorities without significant investigation. Furthermore, he reported to me that any practicing physician in Canada who goes public with concerns about vaccine safety is subjected to a storm of derision from academic physicians and potential termination of employment (state-controlled socialized medicine) and loss of license to practice.”
Ask yourself, if the vaccine is so safe, why would they need to resort to intimidation tactics like this? And how can they determine that the death couldn’t be due to the vaccine without a thorough review?
Interview of Byram Bridle who filed the FOIA request that showed the biodistribution data that was previously kept hidden by the drug companies showing the S1 protein is being made inside all organs of your body. It crosses the blood brain barrier, it accumulates in your reproductive organs, etc.
If I were forced to take these vaccines today
The S1 subunit is toxic. To minimize the damage to your blood vessels and minimize clotting due to this toxin, if I were required to take the vaccine, I would pre and post medicate with:
- Baby aspirin 81mg to reduce clotting (do not use full strength; that is worse due to cox-2)
- 50mg of fluvoxamine once per day to reduce inflammation by activating Sigma-1 including in your brain (this is a lower dose than in trials since it is started before the vaccine)
- D3 65,000 IU twice weekly to reduce inflammation
- NAC 600mg twice a day, to reduce damage to endothelial cells,
- Ivermectin 6mg taken once a day
I would start medicating 3 days before and continue for 3 weeks after which very few spike and free S1 subunit cells will be circulating. These are lower doses than you’d see in treatment protocols
Basically this vaccine is mini-COVID and to prevent damage and inflammation, these are the drugs I would take because they are individually proven to be effective and they don’t interact.
What academics think of this article
Here are comments I received:
- Happy to promote if published in peer reviewed journal
- Without large randomized double-blind controlled studies, you cannot make any of these assertions.
- Your stories about your physician friend are just anecdotes and must be totally ignored (even though we cannot explain them). The plural of anecdote is anecdotes, not data.
- There could be other causes for all these strange side effects (that I cannot think of at the moment but that doesn’t mean that they don’t exist). You haven’t proved causality.
- If you want your physician’s anecdote to be believable, it must be published in a peer reviewed journal.
- The New York Times is not a primary source. Just because they reported dozens of cases of myocarditis in teenagers shortly after vaccination doesn’t mean it is true. You need an authoritative source for this, and the CDC didn’t disclose the numbers. So you can’t really say the numbers are high. The fact that Israel found the same high event rate is simply a coincidence, not proof.
- Since the V-SAFE statistics are a closely guarded secret, you can’t make any claims as to the rates of serious adverse events.
- Without knowing the denominator on the VAERS data, it is impossible to make any conclusions. It could be people are just reporting more often than in previous years.
- The VAERS data is unverified. You cannot prove any of those deaths were caused by the vaccine.
- I find your arguments completely unconvincing and you should trust the authorities. You are jeopardizing lives. Please do not email me ever again.
Typically, people will zero in on one detail. This technique is known as “cherry picking.” If that one point is insufficiently proven in their mind, then that gives them the justification to ignore everything I’ve written here even if it is all true.
My response is:
- I showed you my analysis. May I see yours?
- May I see your proof that the spike protein and S1 subunit are harmless?
- If our biodistribution data is wrong, are you saying Pfizer lied to the government?
- How do you explain the excess deaths? The sky high rate of pericarditis and myocarditis for teenagers? The high disability rate?
- How can telling the truth endanger people’s lives? I am calling for transparency and informed consent. That is a good thing when I believe people are being unnecessarily harmed by being deceived into thinking this is a safe vaccine.
- I’m happy to correct any inaccuracies if there is evidence showing I’m wrong.
- Doctors are too busy with patients to assemble the data. They hope others will.
- Experts like David Wiseman who discover flaws in studies cannot get his papers published. In general, if you go against the narrative, you are unlikely to get published since the peer reviewers are vested in preserving the narrative (note, this is fortunately not 100% effective, but consider Pierre Kory and Frontiers: the paper was rejected after passing peer review).
- No academic who told me what I was doing was wrong could show me the vaccine is safe. Their proof was essentially that if it was unsafe, that the CDC would have stopped it. Clearly, the CDC isn’t stopping it, but everyone knows that there are dozens of vaccine reported incidents with teenagers developing a heart condition that requires 6 months to recover from. And people know that there are 4,200 and likely more completely unexplained deaths. This is unprecedented in our history that a vaccine can kill that many people and we look the other way. Whatever happened to “do no harm”??
- It is completely baffling that the death toll from ivermectin and fluvoxamine over the past 50 years is less than 5 people (as far as I know). Yet the NIH and WHO considers these drugs too unsafe to recommend despite overwhelming evidence (including an extremely well done Systematic Review on ivermectin (which is the highest level of evidence in Evidence Based Medicine) that these drugs work. The NIH even knows that both drugs were recently confirmed in a large high quality clinical trial done by a top university and superb researchers that they claimed they were waiting for. So how can drugs that collectively have killed < 5 people in 50 years be considered unsafe, yet a vaccine that has already killed at least 4,200 people in the US and at least 12,000 people in Europe be considered “safe and effective.” Nobody has been able to explain that one and I’m still waiting. They justify it because “the vaccine is better than the virus.” No it’s not if you tell people to treat early with ivermectin and fluvoxamine or any one of a number of protocols that doctors have developed (such as from Peter McCullough, Fareed and Tyson, etc). Early treatment works but is being suppressed by the NIH and WHO. There is no reason for that suppression. That is what is costing lives, not my opposition to a dangerous vaccine.
- This is a pandemic. The Precautionary Principle of medicine requires you to look at all the evidence in front of you now and decide which hypothesis fits the facts best as to why this vaccine is killing people so as to minimize the loss of life. Do you have a better explanation for everything here? The hypothesis I present fits the facts to a “t” and explains why people are being severely disabled or dead.
- The reason you don’t hear of the death and disability from this in the mainstream media is people are told not to talk about it and the press won’t cover it. How can the press decide whether a given side effect or death was attributable to the vaccine. You can’t prove any single case. So all are not reported. But what you can prove is that the adverse reactions from this vaccine are off the charts, but the mainstream media cannot report that because if they did, then it would be an admission that they helped mislead the public into taking an unsafe vaccine that has now killed at least 16,000 people if not more.
- If this vaccine caused a single event like heart attacks, it would be easy to track. But the events are diffuse and random…. where your blood clot will happen is unpredictable. The computers that analyze events are looking for a statistically significant rise of a single event; they never really designed these early warning detection system for a vaccine that causes such a broad range of adverse events.
- The longer the mainstream press looks the other way and insists nothing is wrong here, the more they will lose our trust.
- Vaccines are supposed to be safe. You are not supposed to die from a vaccine. If you argue that death by vaccine is less than death from the virus, then disclose the fact that this vaccine can kill you, tell them the TRUTH about how effective early treatment is, show them the stats of Fareed and Tyson, and let them decide whether to risk their lives on a vaccine that kills and disables people vs. a treatment protocol (like Fareed and Tyson and others) that turns the virus into a minor inconvenience.
- VAERS data: That’s why I made this video which is really hard to dispute showing a 100X greater death rate in 30 year olds (who don’t normally die). Also, where did you see the analysis of these death reports by the drug manufacturer showing they were unrelated to the vaccine? Excess deaths like this do not just happen by “accident” or “chance”. So if it wasn’t the drug, what was it?
- If you don’t believe me that this is 100X more deadly than the flu vaccine, do you have any proof of the opposite that the death rate for this vaccine is no different than for influenza? I’d LOVE to see that! If it exists, why isn’t it being disclosed? Lots of hidden evidence here. I wonder why??? Hmmmm… If there are no SAEs, transparency reduces vaccine hesitancy.
- If you disagree, please show me any fact that disproves what I wrote, e.g., here’s proof that your doctor didn’t say that. You are doing a disservice to the public by not telling me any mistakes. I’d love to be proven wrong here, but thus far, all the academics say “I’m not convinced” but they bring no proof of their own to the table, e.g., here is the actual death rate based on the analysis from the drug companies.
In short academics put a very high bar in place and if you cannot rigorously prove your position, they will not change their currently held belief system, even if they cannot produce any evidence to support it. The burden is on me.
None of the academics cited any evidence disproving anything I wrote. Basically they said I was wrong and shouldn’t have written the article. They would not cite any facts to support their contentions or even point out any statement that was wrong (even after I asked them explicitly).
In short, they tell me I am wrong, cite no errors in what I wrote, and suggest that I remove my post and change my position. But in order to get them to change their mind, large double blind randomized controls trials are required. This seems a bit lop sided. But there is a reason for this asymmetry.
For many of them, this article is extremely uncomfortable. They don’t have any facts to disprove it, it makes perfect sense, objective smart people find it convincing, yet the academics all reject it. Why? I think because it makes them look silly for supporting the myth that this vaccine is perfectly safe. Nobody likes to be proven wrong. Therefore, they will not evaluate this article objectively: they will instead seek to prove it must be wrong because it conflicts with their beliefs. If you challenge any existing widely held belief, strong evidence is required.
How an academic would argue for the vaccine
They claim: The jab will result in a lower total death rate even if there are side effect.
I claim: Early treatment results in better outcomes than the vaccine (fewer deaths, fewer side effects). Also infection rates are lower since 50% have been vaccinated. The chance of serious event are lower for treatment than vaccination.
So their arguments only works if early treatment doesn’t exist.
Without early treatment:
Vaccine: 300M people *.0002 = 60,000 dead from the vaccine itself
COVID: 300M * 10% catch covid * 10% hospital rate * 10% death rate = 300,000 dead from COVID
So if your early treatment gives you a factor of 5 or more, you win. With a single drug you can get 10X or more. With multiple drugs you get 100x or more.
So early treatment wins. You never cause a healthy person to die and lower death rate.
Is everyone so brainwashed that independent thinking is gone?
In order to find out the answer to this question, I stopped by a vaccine site at the drug store. I asked “Does anyone know how many people have died from the vaccine?” People were insulted by the question, called me an anti-vaxer, told me how they believe in God, and called for the management to remove me from the premises.
Wow. I wish I had this on video.
So be careful. If you question “the narrative” you will get shut down. It felt to me like mass brainwashing and independent thinking was gone. People have total trust in authority. As this document shows, that is a huge mistake.
How did we get to this point where people are looking the other way and punishing truthtellers?
Is vaccination an evil conspiracy to kill people? No. It’s simply a combination of mistakes by Fauci, the drug companies, and bad assumptions by the FDA, and a lack of good safety monitoring by the CDC.
- Fauci was funding the gain of function research in Wuhan. We don’t know what the real purpose of that research was. But we do know there was a cover up when the virus escaped. Chris Martenson analyzes the evidence here. How can all the experts believe it was man-made and then a week later they write a paper saying it was natural origin? Why is Jeremy Farrar on these emails? Why was the stuff redacted improperly? What was in that redacted part? So basically there was an accident where the virus got out. That was unintentional accident, but now Tony has to cover up that it was his fault.
- Fauci then screws up by ignoring early treatment and putting all the chips on the vaccine. He doesn’t invest anything in that area.
- When ivermectin and fluvoxamine are shown to work, they make sure to use the regular evidence based medicine criteria instead of the precautionary principle and use all available evidence. This keeps these solutions out of sight. Otherwise Fauci looks bad for spending all that money on a vaccine we never needed in the first place.
- They rush the vaccines to market. They leave in the PEG and they believe the spike protein and S1 subunit are harmless antigens.
- Everything looks good in the phase 3 trials since given to really healthy people who have never had the virus.
- Adverse events are all over the place…not concentrated in one type of event. The safety signals never trigger so everything pats themselves on the back.
- Doctors don’t associate all the weird side effects with the vaccine so they don’t get reported
- Everyone legitimately doesn’t know the vaccine is dangerous. Looks safe. So doctors who oppose the narrative are ostracized. So docs keep their heads down and “ignore” the events.
- The CDC’s tracking systems never figure out the safety signals since it is so random and diffuse
- Outsiders like me discover that my carpet cleaner and his wife are both disabled by the vaccine. That cannot happen by chance with a safe vaccine, so I start looking into it.
- I attend a CCCA meeting where Dr. Byram Briddle presents the biodistribution data from Pfizer obtained under FOIA. Whoa! The vaccine is NOT confined to the shoulder. It goes everywhere and causes inflammation and blood clots.
- I call Robert Malone with this info. He tells me about PEG and how that short cut proper safety by not doing proper toxicology study and leaving in the PEG.
- I write this doc and notify the FDA they have a problem.
- FDA says no safety signals tripped so they will take no action.
- I publish the doc on trialsitenews and it goes viral. Nearly all positive comments.
- I ask people for mistakes. One guy says I shouldn’t recommend aspirin (which is legit), so I change it.
- TrialSiteNews reaches out for comments from NIH and WHO. WHO ignores them. NIH refuses to comment.
- CDC still can’t figure out why anyone died or had myocarditis and pericarditis.
- I appear on a popular podcast and the viral story goes super-viral [ I predict this]
So they made a mistake and still haven’t figured it out that they have a problem. They know they can’t explain the deaths, blood clots in the brain, etc. but it’s OK because nobody else is asking questions since the press is asleep at the wheel or doesn’t want to disturb the narrative (since that will make them look bad for earlier pushing the vaccine). So as long as everyone plays along, it looks like it’s a perfectly safe drug and nobody has egg on their face.
If someone like Joe Rogan or 60 Minutes tells the story, then they have to decide whether to admit the truth, or double-down to try to keep the false narrative alive for as long as possible.
So here’s the thing… the truth will eventually emerge just like Fauci and gain of function. At that time, Fauci becomes the fall guy and he gets taken out and all the others deny culpability saying “We trusted him…Who would have known?”
How NIH will respond to the issues raised in this article
It is so predictable. They will issue a statement like this: “The National Institutes of Health and National Institute of Allergy and Infectious Diseases are focused on critical research aimed at ending the COVID-19 pandemic and preventing further deaths. We are not engaging in tactics by some seeking to derail our efforts.”
The problem with this is if anyone looks at that it is clearly a dodge. I’m the guy who funded the fluvoxamine trial and promoted its use with ivermectin. The NIH stood in the way of this approval even when they learned the large phase 3 trials confirmed it. They cannot argue the trials were not well designed because the WHO has already acknowledged they were. So they have no leg to stand on and I will expose them if given a chance. Denying the truth will further harm the reputation of the agency. They know I’m telling the truth and that’s why they will never debate me. Because they will lose.
The proof is simple. Have the press ask them the questions listed in this document and see what they say. They are embarrassing questions for the NIH and WHO.
VAERS shows 100x higher death rate for this vaccine
Watch this video showing a 100X greater death rate in 30 year olds (who don’t normally die). This is a very convincing video. NOBODY can explain a 100X higher death rate.
The only argument would be more people got COVID vaccine than flu vaccine.
That’s not true.
As of Jun 1 when the video was made, 41% have been fully vaccinated (135M) and 51% have had at least one shot (168M).
CDC stats on flu vaccine show compliance from 2010 to 2019 ranged from 41.7% to 49.2%.
So we should expect to see comparable numbers this year, not a 100X increase.
But the death rate for the influenza vaccine is pretty much zero so these deaths are pretty much just random chance. So this vaccine is much more deadly than that just 100X the influenza vaccine. It could be 1,000 or 10,000; we don’t know because the death rate from the influenza vaccine for 30 year olds is so low it is very hard to measure.
Finally, if you knowingly submit a false VAERS report you could be fined or imprisoned, so the idea that there would be lots of data fabrication seems quite unlikely.
What we don’t know about VAERS is the denominator because we don’t know how under reported these cases are. The 5,000 total deaths reported could easily be 50,000 deaths.
To make a rough guess at the right “multiplier” we ask individual docs for their death rate which averages around .025% so that would be around 25,000 deaths so we should multiply the VAERS data by 5 to get the true number.
Remember that’s only a very rough estimate.
CDC’s early warning system — NOT!
I always thought the CDC has it’s act together. Surprise. They don’t. Their systems are a train wreck.
This should now be obvious to everyone.
They’ve never announced that the vaccine triggers shingles (herpes zoster) infections. This well known inside the CDC, but they haven’t announced it because they don’t want to panic people. But researches found the link too.
The CDC never warned teenagers that they could get myocarditis and pericarditis. Only after dozens of teenagers were harmed by the virus did the CDC let the New York Times know, but instructed them to downplay the numbers to “a few cases.” It took enough parents speaking out to make this happen. The CDC must have known this way before all the parents figure it out. Here is a letter to clinicians in Maryland showing that this is not normal. Here is the CDC page on these reports. They refuse to reveal the number of events and the rate that they events are occurring. We only know this is significant due to the New York Times story.
The CDC’s systems are so messed that they rely on Israel to discover if there are adverse effects. And even Israel was very late to pick up the myocarditis in kids.
Here’s a note I got from someone from “the inside.”
CDC has its traditional states reporting data base. It is a mess. Race ethnicity very incomplete. Some states submit negatives some only positives. The coding 5 is very sloppy. States have vaccination data bases but those are also in a very poorly developed state. The State of California and New York have the best State data systems but the they usually start with claims data and again, the claims were not used during the vaccinations. If some sort of secondary coding from the vaccinations cites into claims is taking place, I do not know. I do know that some clinical systems are trying to bill for their vaccinations in mass settings.
For the over 65 we have traditionally used CMS claims data, but because a lot of vaccination was done in mass vaccination settings billing was not routine. The status of the claims data is poorly understood. The purpose of setting up HHS Protect was to avoid the problem. CDC undermined HHS Protect by focusing on state reporting.
The best data is probably coming from Israel and other countries that actually have functional data systems.
HHS Protect was supposed to fix these problems, but the CDC decided to focus on state reporting which is a mess.
A public, prospective registry would make all of these events more transparent. This will cost $10M to fix. Clearly the CDC isn’t doing it. Someone should. If you are interested in saving a lot of lives and have $10M, you can contact me on LinkedIn.
This is really just the tip of the iceberg here. There is a lot more to tell.
Let’s just say that it is better to rely on what is happening by talking to physicians off-the-record who have large patient bases (over 1,000). Some physicians (500 patients or fewer) can see no significant events.
My biggest complain is the NIH. Relying on the NIH for COVID treatment recommendations has caused the unnecessary loss of life of hundreds of thousands of people. Watch for my op-ed coming up on this.
Nobody has been able to prove the NIH or WHO got their recommendations right, even after my $2M incentive. There was only one entrant, a doctor in Belarus, but he didn’t follow the rules and attempted to prove his case by making up numbers out of thin air instead of analyzing the evidence in the studies.
Still unconvinced? Consider this
This is what your government is incentivizing you to do to your kids. This wouldn’t be an issue if the S1 subunit protein was benign. It isn’t. It is extremely pathogenic. And it is going into the ovaries of our young women. Is this OK? Are you OK that they didn’t tell you about this? This graph reflects the data on Page 7 in “184.108.40.206B. PHARMACOKINETICS: ORGAN”. The document is marked PFIZER CONFIDENTIAL. It is confidential for a reason. We are not supposed to know this because it would create “vaccine hesitancy.”
Also, I said this before and I’ll say it again: I learned from Byram Bridle’s paper (not yet published) there have been some adverse events reported of infants experiencing bleeding in their gastrointestinal tracts after suckling from mothers who had received a COVID-19 vaccine. That cannot happen by chance.
Why are they suppressing the early treatment drugs?
My guess is Anthony Fauci wanting to prove he is right combined with using evidence-based medicine highest standards of proof even in a pandemic and even when the drugs are extremely safe (little downside).
Fauci could have set the right tone to use the Precautionary Principle and use all the available evidence. He didn’t
I used to think he was a God… the guy who stood up for science. Encyclopedic knowledge of infectious disease.
We knew a year ago that the SARS-CoV-2 was man-made when Chris Martenson and others exposed it. It is impossible to explain the sequences because they don’t occur in nature. Guess who funded the work in Wuhan. Fauci. He finally admitted it. This whole thing was his fault.
Insiders told me is he is a superb politician who surrounds himself with “yes-men” like Cliff Lane who is in charge of the NIH Guidelines.
Fauci compounded his error in funding the gain of function research by suppressing the early treatments that would have rendered the virus relatively harmless (less dangerous than the flu) if the NIH had told people to treat the virus early and hard with an effective protocol (just as David Ho advised for HIV).
Fauci cannot allow early treatments to be successful. If people ever find out that we had the solution sitting on the shelf the entire pandemic and it was Fauci who was responsible, it will look really bad.
So Fauci made a bad call by focusing primarily on vaccines early on rather than pursuing repurposed drugs with the same intensity. The coronavirus experts I talked to at the start of the pandemic said that camostat was the most likely drug to try against COVID (it was a tie with remdesivir for early treatment of outpatients). Guess who funded these trials? Not NIH. Not Gates. Me! And guess what? The trial has recruited for a year, the results are in. What the hell is going on? This is a pandemic. What happened?
So I’d guess that Fauci told Lane to require evidence beyond any reasonable doubt that drugs work even if they are as safe as over the counter meds and supplements. That’s NOT what you do in a pandemic. If you have a sign that safe drugs work, you use them. Watch this 1 minute video of Michael J. Ryan who is head of the WHO COVID response. He tells people:
- You need to react quickly. Be fast. Have no regrets. You MUST be the first mover”.
- “The virus will always get you if you do not move quickly.”
- IF YOU NEED TO BE RIGHT BEFORE YOU MOVE – YOU WILL NEVER WIN”.
- PERFECTION IS THE ENEMY OF THE GOOD WHEN IT COMES TO EMERGENCY RESPONSE MANAGEMENT.
- SPEED TRUMPS PERFECTION.”
- “Everyone is afraid of making a mistake. Everyone is afraid of the consequence of error, BUT THE GREATEST ERROR IS NOT TO MOVE.
- THE GREATEST ERROR IS TO BE PARALYSED BY THE FEAR OF FAILURE.”
Fauci and Lane do the opposite of what Ryan advises. Their actions have not saved lives. Even after there are 29 published studies all positive on risk-benefit when used early, they give that drug a DO NOT USE recommendation. It’s bizzare.
In a pandemic, it is essential that authorities use the principle of all the available evidence to make recommendations using the Precautionary Principle and not wait years for large scale phase 3 clinical trials.
The NIH knows all about the Precautionary Principle because that is how they justify mask wearing when none of the research supports it. So they use it when convenient for them, and they ignore it when it makes them look bad.
There was a Cochrane review of the mask wearing studies. It concluded:
Medical or surgical masks
Seven studies took place in the community, and two studies in healthcare workers. Compared with wearing no mask, wearing a mask may make little to no difference in how many people caught a flu-like illness (9 studies; 3507 people); and probably makes no difference in how many people have flu confirmed by a laboratory test (6 studies; 3005 people). Unwanted effects were rarely reported, but included discomfort.
Four studies were in healthcare workers, and one small study was in the community. Compared with wearing medical or surgical masks, wearing N95/P2 respirators probably makes little to no difference in how many people have confirmed flu (5 studies; 8407 people); and may make little to no difference in how many people catch a flu-like illness (5 studies; 8407 people) or respiratory illness (3 studies; 7799 people). Unwanted effects were not well reported; discomfort was mentioned.
Do physical measures such as hand-washing or wearing masks stop or slow down the spread of respiratory viruses? Nov 2020 Cochrane
There was only one randomized study done on mask wearing for COVID. It found a small benefit (18%), but the 95% confidence interval was wide enough that masks could be harmful: 46% reduction to a 23% increase in infection.
I’m not suggesting that we should stop using masks, but the point is that the mask mandates were done even before a single study was done. The NIH and CDC still don’t have a single large randomized Phase 3 clinical trial showing that mask wearing is effective. So if that is a mandate based on expert opinion, why is fluvoxamine given a NEUTRAL when the experts say it should be discussed and all the studies published to date (June 2, 2021) show a statistically significant benefit and all the other evidence shows a benefit as well? Same can be said for ivermectin and other drugs. The hypocrisy is glaring and inexplicable and NOBODY will debate this in a public forum (TrialSiteNews has asked the WHO and NIH and Cliff declined without giving a reason and the WHO did not respond). Only Congress can make them answer to this but nobody in Congress is doing that.
By selectively ignoring these life-saving principles, Fauci and Lane are both huge liabilities and their collective lack of judgment have cost the lives of hundreds of thousands, if not millions of people worldwide. And if they want to sue me for libel, bring it on because truth is the ultimate defense here and they know I know that they know that these drugs work and are withholding that from the public.
When the fluvoxamine study was confirmed in a second quasi-randomized study at a racetrack showing 100% protection from hospitalization and long-haul COVID, Fauci should have shown up on site and verified that this very credible researcher’s study was valid or not. The p-value on the symptoms alone was 1e-14 which is impossible to happen by chance. And the quasi-randomization was more convincing that true randomization because the sicker people chose the drug. There was no observer bias since every observer saw the same differences (including the track management who weren’t involved at all). So now you had two trials, p values both <.01, done independently with the same 100% effect size. While you could argue that it doesn’t meet traditional evidence based medicine rigorous standards, any normal thinking person would embrace this result.
60 Minutes showed up and spent hours investigating and telling the story. If there was a flaw, they would have pulled it.
What did Fauci and Lane do? They treated the two studies, both with 100% effect size, as insufficient. What could have caused these results if not the drug? Doesn’t matter to them; they don’t have to come up with a plausible hypothesis as to why the drug should be NEUTRAL. My attempts to brief Fauci: ignored. And I didn’t just email him directly. I had one of his high level friends tell him just to make sure he got the message.
Even after the 60 minutes story, no contact, not with me, not with the researcher. NOBODY at NIH lifted a finger to verify the study was legit. This is a pandemic. If there are two studies, both with 100% effect size, both done by top researchers, both published in top peer reviewed journals, both given “Editor’s Choice” designation, and both studies appear on 60 Minutes, you don’t ignore it. What kind of a person would do that?
Why didn’t the NIH convene an expert panel to review the evidence when this happened? They basically just said, “let us know when you have a large Phase 3 trial.” In short, deaths of people in the meantime don’t matter. They want to make sure they aren’t wrong. Minimizing deaths in the meantime are irrelevant to them.
Dr. Jeffrey Klausner took action. He convened an expert panel of 30 people from NIH, CDC, and academia which examined the evidence including the plausible mechanisms of action. The scientists asked questions. There was discussion. The survey afterwards showed that an overwhelming majority (more than 2:1 ratio) recommended that doctors talk to their patients about using fluvoxamine.
You’d think the NIH would instantly list fluvoxamine with a positive recommendation since expert opinion was positive. They did not. Nothing kept them from having a FOR recommendation. There was no law that would have prohibitied this.
The NIH then waited 3 months before adding fluvoxamine to the guidelines with a NEUTRAL recommendation on April 23, 2021. This is interpreted by doctors as “do not use” and the NIH knows that. This is why you don’t see fluvoxamine on any government guidelines anywhere else in the world and why if you ask your doctor for a prescription for fluvoxamine they will refuse to prescribe it off-label even though they could and it is perfectly safe when properly prescribed as this Kaiser doctor demonstrated:
I have told Cliff Lane on numerous occasions that there is not one shred of neutral or negative evidence on fluvoxamine, every study shows a positive effect. I said “you cannot find a doctor anywhere in the world who has used tried this drug on more than 1 patient who thinks it doesn’t work.” The opposite is true in fact; the doctors who have used fluvoxamine have told me that it is unethical not to use it.
But all this evidence are anecdotes to Cliff. I could have 100 docs with zero hospitalizations and that’s all anecdotal to him. There is NO NEUTRAL OR NEGATIVE EVIDENCE Cliff. Zip. Nada. None. All the evidence is positive (two in a row with 100% effect size) and the drug has a 37 year safety profile and we know there are no long term negative effects when used for COVID from the WashU study of fluvoxamine. In the DB-RCT, if you took the drug you had fewer side-effects than placebo.
Cliff Lane is a disaster. His lack of actions on fluvoxamine, ivermectin, and other effective drugs are not defensible. Nobody else will defend him either: Nobody has been able to prove the NIH or WHO got their recommendations right, even after my $2M incentive.
Do you have a vaccine side effect?
Facebook shut down all your groups, but TrialSiteNews will host your forum. Please report your experiences with your symptoms, whether they are resolved, what your doctor told you was the cause, etc. at the TrialSiteNews Vaccine Side Effects forum where you will not be censored and spread the word.
A very troubling email sent to Dr. Bridle
Have you ever seen an email like this as a vaccine reaction? How many more emails like this must be sent before Congress takes action to stop vaccinating our children?
Hi Dr. Bridle,
I heard your interview today.
My 16 year old healthy sister-in-law was in ER today. (Alberta)
She couldn’t talk or read this morning.
Docs don’t connect dots but I told mother-in-law to demand testing. They found markers to indicate clotting in blood. Further CT testing didn’t reveal any they could see. Her neurological issues improved enough but she feels spacey. They sent her home blaming stress and perhaps her birth control. She had the Thing 48 hrs ago. Pfizer.
Any recommendations of or info you can send is helpful. She’s not on any blood thinners but was on Accutane (does it thin blood? I know it has nasty side affects as well).
Email sent to Dr. Byram Bridle on Saturday, May 29, 2021 1:02 AM after this interview
A personal note
Do you know anyone with significant adverse events from other vaccines? I don’t.
The anecdotes I’ve heard from this one are off the charts. Doctors tell me the same. The range of symptoms are unprecendented… serious weird things that are extremely rare all pop up after vaccination like “loss of all feeling in both arms at night only” or inability to see and speak (on a 16 year old) after vaccination. When was the last time you heard that happening.
Let me tell you how I got suspicious something was very wrong. Because of the pandemic we have had very few visitors to our house, maybe around two dozen total. Tim Damroth, my carpet cleaner, is one of them. He is 38 years old and in great health. He got the Pfizer vaccine on April 26 and he had a heart attack 2 minutes later and spent the night in the hospital. On May 23, 2021, he sent me an email, “Last night my head had mild tremors. This morning my left arm at the injection site is in agony. I’m fatigued, and I’m seeing my doctor Monday. Who in the press will listen to me? I’m furious.”
Indeed, Tim was frustrated that all his attempts to let others know were ignored. I even tried my press contacts as well. Ignored.
Tim almost died in the hospital recently. He sent me a note telling me to bring his story to the attention of the press if he died so his death would at least warn others.
He’s still alive. He is extremely impaired. The doctors don’t know how to restore his health.
Tim’s wife, Monique, got the Pfizer vaccine in March and now her left arm shakes like she has Parkinson’s disease and it’s still shaking today, 3 months after her shot. Her tremors are improving, but the pain is getting worse.
Both of them are disabled. If the vaccine is really as safe as they claim, such anecdotes where both husband and wife had adverse effects would be extremely rare.
Did I just get “unlucky” that, with so few visitors to our house, we had a husband and wife with serious vaccine side effects? It’s certainly possible, but unlikely.
The press wouldn’t report either of these events. They won’t report on any of them because you can’t prove a single one. Same for deaths. They won’t say it is vaccine related because they can’t prove it is.
Why aren’t the autopsies revealing the true cause of death? Because nobody has the equipment to measure S1 subunit spike protein (except at fancy research labs like at Harvard). So they report the cause of death was a heart attack or blood clot in your brain.
Tim’s case suggested to me that the rate of serious adverse events could be quite significant. Tim’s case led me to look further under the covers and the more I looked, the more appalled I became. I wanted to document what I found since the press would not talk to Tim. That’s why I wrote this document.
Remembering the victims #covidvaccinevictims
There are countless stories like this. You never see this for the flu vaccine. Nobody dies from the flu vaccine.
Here’s a note I got on one of my twitter posts:
Others have written about the censorship. If you challenge the narrative for early treatment and talk about repurposed drugs, all the social networks will remove your posts or videos, ban you, demonetize your videos, suspend or cancel your accounts, or make sure your posts have limited distribution. Appeals are useless. Sendgrid will remove all your contact lists if you send an email they don’t like, even to your private contacts. Medium will ban you for life for talking about fluvoxamine and ivermectin as safe and effective treatments for COVID. When I asked them for facts, they just wrote back that they considered my post to be dangerous.
Doctors and patients are censored. Doctors are intimidated and told not to ascribe deaths to the vaccine.
Dr. Chris Martenson creates excellent videos, but he has to spend enormous amounts of time to figure out how to present information in a way that can escape censorship by YouTube. How can he do a video that explains why you shouldn’t be vaccinated if he can’t talk about it? Muzzling people who are clear thinkers like Martenson is the very last thing a civilized society would want to do, yet here we are.
It is the social media and mainstream media that perpetuate the myth. They are as dangerous as Fauci himself. They empower the false narrative of the NIH on early treatment leaving the vaccine as the only choice. They will not debate their decision. There is no impartial jury.
It’s one thing to remove posts and videos with no basis in science. But removing content created by doctors that is scientifically supported just because it goes against the “popular narrative” promoted by “experts” is no helpful and has cost thousands of lives.
Censorship should be a user preference. If the user trusts the platform’s censors, great. But if users don’t want censored content, they should be able to see everything without filtering.
The other censorship is with the medical journals. How is a flawed study on Ivermectin singled out for publication in JAMA when very well done ivermectin studies are rejected? David Wiseman discovered if you correct the errors in David Boulware’s paper, HCQ works. But the journals reject his paper.
Quora has been outstanding through all of this. From day 1, they have been supportive of people such as myself who are truth tellers. The top management of Nextdoor also should be acknowledged here for doing the right thing in supporting legitimate freedom of speech. LinkedIn has also come through in restoring posts from the FLCCC that were erroneously censored. YouTube has been a mixed bag, in restoring some videos, but mostly removing helpful posts.
I am proud of hundreds of scientists who speak out against the narrative. For example, see Robert Malone’s article. Remember, Malone isn’t some random dude; he the inventor of mRNA vaccines and he thinks this vaccine is a danger to society. Peter McCullough is another outspoken truthteller. Despite being a very credible scientist, his views would be censored from YouTube so his video is here. Nobody will dare debate him.
Pierre Kory is another tireless advocate for the truth about early treatments. He is “Mr. Ivermectin.” George Fareed and Brian Tyson who have been pioneers to prove early treatment works. David Seftel, Emory Dean of Medicine Vikas Sukhatme, the list goes on and on. I am honored and proud to count all of these people as my friends.
Most of all I am grateful to Daniel O’Connor and TrialSiteNews. They have been supportive from Day1.
The case against Fauci
To sum it up from my points earlier in this document:
- He funded the research that created the virus. He even lied to Congress, but was later forced to recant. Watch this video of Dr. Chris Martenson taking down Fauci. It is priceless. Chris mentions me at 47:30.
- His emails reveal he knew it came from the lab, then met with others to cover it up. Why was Jeremy Farar involved in all those emails involving Fauci and the coverup?
- He caused the NIH to suppress funding of early treatment research
- When others like me funded early treatments and proved it worked, he made sure the guidelines were neutral to negative (by directing Cliff Lane to keep early treatments as unapproved for as long as feasible even after they knew these drugs were confirmed in large credible Phase 3 trials) so nobody would use them leaving the only option: a vaccine
- He was cheerleader #1 of the most deadly vaccines in our history which although would save lives, has a huge cost in death and disability beyond anything we have ever seen; there are safer, more effective alternatives that people were not told about.
- He continues to ignore the overwhelming evidence for early treatments like ivermectin and fluvoxamine which have been clearly shown to have very little downside and superior efficacy, leaving people with only one alternative: the deadly vaccines.
This is hardly the first time. I just got this on Twitter:
Sadly, Fauci has been this way for decades. Covid is a repeat of his response to the AIDS epidemic, but now is on on a larger scale. His trash guidelines for Lyme disease have left patients disabled for decades. He should have been exposed long before this.
Anthony Fauci said it himself in an email: “”Our society is really totally nuts.”
Everybody makes mistakes. The mark of a great organization is how they react once the mistake is known.
There were no evil players at the FDA. Everyone thought the S1 subunit was a benign antigen. They knew about the biodistribution but it was deemed irrelevant since the antigen is benign.
I am a huge fan of Janet Woodcock. She has been extremely responsive to the information as it became more and more clear. I’m sure the FDA will do the right thing. I really cannot say enough good things about her. She is a tremendous asset to the FDA and to the country.
The 100X flu vaccine rate observed here means that virtually all the excess deaths were caused by the vaccine. When was the last time the FDA allowed a drug to kill 20,000 people worldwide in 6 months?
At a minimum,
- there should be a black box warning for the vaccine that is immediately put on the label and in the informed consent that when used as directed, it can kill you.
- Due to the accumulation in the ovaries, the drug should be halted for all pre-menopausal women immediately until we can assess the safety of the drug.
- The drug should also be halted immediately for those under 20 since the COVID risk of this group is minimal, the drug has been shown to produce severe adverse reactions, and early treatments have been proven to work so there are viable safe alternatives (once Fauci is removed and the NIH can see more clearly).
Let’s look at a few drugs pulled off the market due to death rate:
- Duract: This pain killer was effective in relieving pain, but it caused 4 deaths, 8 liver transplants, and 12 cases of severe liver damage in the year it was on the market. It was prescribed to 2.5M people and caused 4 deaths. Like the vaccines are today (due to early treatment protocols), it was a drug that no one needed.
- Troglitazone (Rezulin): Treatment with this antidiabetic and anti-inflammatory drug resulted in 90 cases of liver failure and at least 63 deaths. Over 500,000 people used the drug.
I think I can stop there. There are probably better examples but the point is that with early treatments the drug isn’t needed and it is causing excess deaths that are above previous thresholds needed for revocation.
One thing that is important to add is the FDA is still in the mindset that they ignore anecdotes. Nobody can explain the excess deaths but they are there and we are killing people. Nobody can explain the range of symptoms. We can.
There are too many physicians (not cherry picked but picked at random) that have SAE event rates of more than 1%.
In the current pandemic, you cannot just rely on your “trusted” data sources because the data is under reported. You MUST go out and verify the reality matches the data. It doesn’t. So who do you believe? The doctors in front of you or the “data”.
Early treatment can reduce COVID death rates by 100 as they can verify by inspection of records of Fareed and Tyson’s records. That’s real life data. So that alone turns COVID deaths into a fraction of the number deaths per year from the flu.
It is better to employ drugs that make sick people well than to make well people sick.
The NIH is where the problem is: NIAID specifically. The NIH Guidelines should be about saving lives, not scientific perfection. Suppressing early treatment research was a mistake beyond belief and compounding it by continuing to not change the guidelines is inexcusable. The root of the problem is Anthony Fauci. He must go along with Cliff Lane. Fauci should be replaced by someone who walks the talk of Michael J. Ryan that mistakes are OK and the important thing is to act quickly and make decisions that minimize the loss of life even if it means having to admit you were wrong on occassion.
I’ve heard that Rochelle Walensky is a good person. She inherited a large complex organization with a lot of dysfunction. I do not blame her for what happened. I have some suggestions on how to fix some of these problems she faces.
The single most important thing she can do is make the V-SAFE database open access. If the vaccine is so safe, why is this hidden from public view?
But V-SAFE is also very problematic because we haven’t told people how the vaccine really works and to report ANYTHING that is “unusual” for you. Right now if my right toe is numb or my hand shakes uncontrollably, I may not associate it with the vaccine, but once I knew the virus engulfs my entire body with a toxic protein, I’m more likely to report it as being relevant.
We know exactly how many people have been vaccinated and make that available. Why aren’t we making the number of people who have died or disabled after taking the vaccine public as well? Full transparency.
Congress is the enabler of Fauci. Fauci doesn’t report to Francis Collins (that’s just on paper, not reality). Fauci is enabled by Congress. If they fail to remove him, people will continue to die.
The biggest problem is nobody in Congress, with the exception of Senator Rand Paul, thinks Fauci is anything but an angel. Even President Biden and the White House are clueless. Biden is moving ahead full speed to vaccinate 70% of Americans despite all the death and disablement. It’s baffling. Fauci can lie to Congress and he’s still an angel. Are you kidding me?!?!
Congress needs to wake up and talk to people outside NIH who used to work there to find out what is really going on.
This should not be a partisan issue. One member of senior Senate staff wrote me after reading my article, the problem is “the complete deference to NIH/FDA/CDC, and the lack of interest in early treatment, natural immunity, etc,”
That’s a good starting point.
It is also remarkable that nobody in Congress has called for a special outside task force to look at the pandemic response and make recommendations for what needs to change for “next time.”
If next time is a virus like in the movie Contagion, we are all doomed. This pandemic was just the “dress rehearsal” for the real thing. It was a “shot across the bow.”
Personally, I have list of over 50 things that could be changed that would really make a difference the next time, but it doesn’t really matter because there is no panel to consider my recommendations. Once the crisis is over, we go back to our old habits.
I tried to get the WHO to look at the fluvoxamine studies. They weren’t interested. Fluvoxamine isn’t even mentioned on their guidelines anywhere. Like it doesn’t exist. Yet it is (as of June 2) at the top of the list of the most promising drugs (the topmost approved drug).
The WHO is seriously broken. They had no outpatient trials at all. Ever! That’s ridiculous because you always treat a virus as early as possible, everyone knows that. What drugs did they test on outpatients: None.
They only tested drugs for inpatients without first having any anecdotal data to support that.
When the SOLIDARITY trial was announced in March 2020, I wrote a Medium piece on how dumb their drug candidate choices were; that they couldn’t possibly work. Medium censored my article. In Feb 11, 2021, they published a paper showing I was right: all the drugs were losers. $100M down the drain and they lost a lot of time. Stupid.
I tried to suggest they do outpatient trials with drug combos like ivermectin and fluvoxamine. For inpatient use, I suggested inhaled adenosine and cyproheptadine would be very strong agents to test with unbelievable consistent anecdotal data.
The told me to pound sand and never email them again.
Medical schools, Medical journals, Academia
The evidence is undeniable. This is not about whether my analysis is right or not. This is about over 20,000 people who were killed by the vaccine. And many times that number who have been disabled or permanently injured. All of the death and disability was completely unnecessary as early treatments have been known for a long long time, well before the roll out of the vaccine.
Will any Medical Schools be brave enough refuse to vaccinate people? Or will they blindly follow the CDC and NIH directives even when they know it is killing people? That’s the big question.
One of two things will happen here:
- The medical profession will just “say no” to this vaccine now and put a stop to this unnecessary mass slaughter
- The medical profession will have their reputations damaged irreparably for failing to recognize the evidence in plain sight
That’s an question the medical community will need to decide very quickly. I believe there will be a massive split happening very soon and we will see leaders emerge.
Finally, it has to be extremely embarrassing to the medical community that an MIT electrical engineer figured all this stuff out rather than someone from the medical field. Why was it obvious to me 7 months ago that ivermectin and fluvoxamine were effective drugs when NOBODY else in the medical community could figure it out (other than Vikas Sukhatme and David Seftel)? There is a big lesson about using all the available evidence and the Precautionary Principle in a pandemic that the entire medical community still needs to learn. People lives are important yet evidence-based medicine doesn’t take into account the probability and the costs associated with being wrong. If this pandemic were as epic as the one in the movie Contagion, we would all be dead. The medical establishment should ponder that one before it is too late.
Employees of Facebook, YouTube, and Twitter
If Facebook had not removed multiple the “Vaccine side effects” groups, totaling over 200,000 people and probably more (I just head of a 120K member group and a 70K member group), there would have been ample evidence in plain sight of the harm caused by these vaccines. Facebook has contributed to this unnecessary loss of life through its censorship. Although it is unlikely the corporation will change its ways, that doesn’t mean that Facebook employees have to just sit there and do nothing. If Facebook employees were to all take a sick day off to read this article, it would send a clear message to Facebook management that suppressing truth and restricting the free speech of victims of a vaccine that was rushed to market is unacceptable behavior.
There is no question also that Congress needs to regulate the censorship of these companies since these networks are the new “public square” replacing traditional common carriers. If these platforms want to arbitrarily censor people telling the truth, there should be a private right of action to sue them for $25,000 for each incident of censorship of factual information.
YouTube isn’t much better than Facebook. YouTube COVID-19 medical misinformation policy is to censor any videos that:
- Content that recommends use of Ivermectin or Hydroxychloroquine for the treatment of COVID-19
- Claims that Ivermectin or Hydroxychloroquine are effective treatments for COVID-19
Are you kidding me?!? For ivermectin, they have no ground to stand on. The NIH has a NEUTRAL recommendation for ivermectin. A neutral recommendation means the doctors get to decide because the NIH panel can’t tell whether the drug works or not. So how can YouTube claim to be “smarter” than the NIH and declare it doesn’t work? Where is the research that they did to prove that the NIH got it wrong? Put it out in public view for all of us to laugh at the sheer incompetence of the people who made that decision. Why do they still have a job?
For hydroxychloroquine, there is no doubt it works if given early enough. 100% of the 29 early treatment studies report a positive effect (13 statistically significant in isolation). Where is your evidence that this drug is doing the opposite? You cannot simply rely on the incompetent analysis of the NIH and WHO.
I offered $2M to any qualified person who could show that the NIH or WHO got it right on their recommendations. No takers. If YouTube thinks these drugs don’t work, then prove it and take my money. If not, change your policy. You are jeopardizing people’s lives here. If YouTube doesn’t do either one, then YouTube employees should stage a sitout until they do the right thing.
As for all the other platforms, if you silence people who tell the truth and who are posting legitimate medical information that can save people’s lives, you are doing a tremendous disservice.
The mainstream media
Just because someone challenges the “authorities” doesn’t mean they are wrong and should be squelched. Op-eds should be judged on their merit, not on whether they were written by a medical doctor. Legitimate points of view, especially those that challenge conventional thinking or challenge authority, should be embraced if they are well supported.
CNN was too busy doing stories on hospitals being full, the dangerous vaccine rollout, and covering the horror stories of lost loved ones that they didn’t have any time left at all to cover the positive story of how Dr. David Seftel went against the direction of the editors of JAMA in order to save people from the mass COVID outbreak at Golden Gate fields. He had a 100% success record in turning patients around (in an average of 3 days to back to normal) and 100% success in preventing long-haul COVID, but CNN was too busy to cover that amazing, uplifting success story. They should be ashamed of themselves. They didn’t want to cover it for fear of “raising false hopes.” Ridiculous. It is news. It is positive news. Cover it, don’t ignore it. Had you bothered to check the p-value was 10-14 which means “it is impossible that the drug didn’t work.” And every single employee at the track was convinced there was a huge difference between the fluvoxamine and no treatment group that 100% wanted the drug. If they can figure it out, why can’t CNN? Of course, writing all this means I’m never going to appear on CNN, but someone has to tell the truth about what they did here. By suppressing these success stories, they contributed to the false narrative that early treatments don’t work.
I am grateful to LA Times, 60 Minutes, and The Wall Street Journal for their courage to run stories and op-eds that enable people to challenge the narrative and bring life saving information to the public’s attention. This is what the media is supposed to do. Bravo!
Bauchner was the former Editor in Chief of JAMA. He just got booted.
It was Bauchner who penned the Editor’s Note that advised physicians not to use fluvoxamine after the JAMA paper appeared because it was just hypothesis generating. That was complete bullshit. The study was confirming a hypothesis generated by many other independent efforts such as the superb work of Nicholas Hoertel in France and Alban Gaultier and his team at the University of Virginia. Every piece of data was consistent that fluvoxamine was safe and effective. You couldn’t find a shred of data that fluvoxamine made things worse or was neutral. And the mechanisms of action made total sense (see the fluvoxamine public data repository).
I emailed Bauchner after Seftel confirmed the original Lenze study in JAMA. I told him, “we confirmed the effect in a second study done by a top researcher; both studies had 100% protection from hospitalization; both were p<.01. Please retract your advice to the medical community not to use fluvoxamine.” He refused and stopped answering my emails. That’s wrong. If he wants to ignore the Seftel’s study, he should have told me why. The p-value for the symptom data in Seftel’s study was 10-14 and that’s a conservative estimate since the study was pseudo-randomized with the sick patients opting for the drug. So there were two independent studies both with p-values <.01 on the primary endpoint (hospitalization). That should have caused Bauchner to at least soften his recommendation, but he refused to budge an inch. This is the kind of medical leadership that we need a lot less of in this country. Good riddance to Howard. I’m not shedding a tear for you.
When he had the chance, Bauchner should have reminded the medical community to evaluate all the available evidence and use the Precautionary Principle to minimize loss of life. Instead he told the medical community to “sit back, and wait a year for them to prove it in a Phase 3 trial.” What kind of doctor are you that would do such a thing? You are more worried about making a mistake than saving lives. You should be ashamed of yourself. What ended up happening was recruitment was so slow they had to abort the trial before statistical significance so we had a solution but nobody would use it because it didn’t have a large phase 3 trial.
It is people like Bauchner and Fauci who contributed to the slow adoption of repurposed drugs that could have ended the pandemic, causing us to rush an unsafe vaccine to market that has resulted in the unnecessary loss of life of hundreds of thousands of people.
There are a lot of heroes in this saga that helped move the ball forward.
Inclusion of their names does not mean they endorse this op-ed. Some disagree with what I wrote. Inclusion simply means that they have been helpful in moving the ball forward and save lives through their efforts.
I cannot order them, they’ve all made a huge difference. Some wanted to remain anonymous. I will take the sole blame for this document. I would not want anyone to lose their job or NIH grants.
Robert Malone, Daniel O’Connor, Peter McCullough, Vikas Sukhatme, Vidula Sukhatme, Ed Mills, Bret Weinstein, Chris Martenson, Pierre Kory, Byram Bridle, Ira Goldstein, Jean-Pierre Kiekens, Joe Ladapo, Janet Woodcock, Jeff Skoll, the Flu Lab, Patrick Collison, Marc Benioff, Elon Musk, David Seftel, Elaine Lissner, Rockefeller Philanthropy Associates, Congressman Bill Foster, Angela Reiersen, Eric Lenze, Glenn Bunting, David Satterfield, Russ Stanton, Thomas Brunner, Hilary Grant Valdez, Jeffrey Glenn, Mary Beth Pfeiffer, Esther Landhuis, Stephanie Seneff, Tess Lawrie, Bonnie Mallard, Steven Pelech, Joseph Vinetz, Juan Chamie, Covid Analysis, Covid Crusher, Josh McLeod, Karen Levins, Mobeen Syed, Syed Haider, Miguel Antonatos, Drew Pinsky, Susan Pinsky, Joon Yun, Sabine Hazan, Ram Yogendra, Robert Likić, Sean Corrigan, Bruce Patterson, Amol Kothalkar, Florian Muller, Peter Meinke, George Fareed, Brian Tyson, Harvey Risch, the FLCCC team, the CCCA team, Jim Roskind, Victoria Yan, Mark Hadfield, Bert Vogelstein, Jovo Vogelstein, Milana Boukhman Trounce MD, John Ioannidis, Susanne Hempel, Jeffrey Klausner, Howard Hu, General Wes Clark, Ken Keller, Gary Dicovitsky, Susanne and Bill Losch. Malathi Srinivasan, Sulggi Lee, Nick Kuel, Eric Osgood, Arjun Bhagat, Peter Relan, Phillip Neustrom, Keletso Nyathi, Joe Giannotti, Flavio Abdenur, Eva Migdal, Alvaro Olavarria, FranceSoir, 60 Minutes, LA Times, The Wall Street Journal, Amy Stoddard, Farid Jalali, Philippe Rola, Tom Hodge, Steven Winston, Sucharit Bhakdi, Phil Harris, Nicholas Hoertel, Alban Gaultier, Jennifer Hibberd, Christy Risinger, …
You get the idea. This was just a partial list.
Permission to copy, distribute, promote
You have my permission to excerpt, copy, translate, repost, whatever. This is all about getting the information out. Feel free to create more digestible versions. I didn’t have time to copy edit this.
Conflict of interests
I do not have any investments that would be affected by this document. I am doing this solely for the public interest. I have a long track record as a medical philanthropist that people such as Nobel Prize winner Elizabeth Blackburn and former MD Anderson President Ron DePinho can attest to (I funded their research 20 years ago).
Feedback I’ve received
It’s all been positive.
You can see for yourself attributable reactions on Twitter so you can see I wasn’t making this stuff up.
Here’s one of my favorite comments.
Here are some more examples. These were private emails or twitter DM.
INCREDIBLE ARTICLE. THANK YOU!
“Steve – this is an amazing article. Pitch perfect. Love the data. Sorry you got vaccinated, let’s hope for the best, but I’m increasingly uncomfortable with it, especially for youngsters. My data says that it has about a 1/2500 chance of turning into myocarditis in youth, skewed toward males, obviously. That’s completely unacceptable! And yet here we are, unable to really talk about that without being hard or soft censored.”
— Dr. Chris Martenson
I’m not getting vaccinated. AVV / AAVV have well known risks of thrombocytopenia. the mRNA ones have understudied risks (LNP cytotoxicity, S1 pathogenicity) and the LNP delivery system does not target only cells with ACE2 receptors — any cell reached can be transfected. Moderna was going out of business until they hit the jackpot because they couldn’t target and other cells hit led to severe direct and immune system effects. Plus, what was their involvement in WIV? Stinks
I talked to two friends. One person was already somewhat opposed to further vaccination mostly due to the nanoparticle issue (a conclusion he reached after having already gotten the pair of shots). He too had concerns about drugs crossing the brain-blood barrier, and also settling potentially in key organs (such as reproductive organs in younger folks that care a LOT more about such issues!). He is a brilliant technologist, and also reads more medical papers than ANYONE I know. He was already pretty miffed about the lack of transparency from the Gov’t. He generally puts a lot of doctors to shame IMO via extensive research. He is also a good “spreader of information,” often based on intense research, but he generally doesn’t go broadly public (re: facebook etc.), as he has no interest in the bucking the cancel culture, and he doesn’t like the privacy invasions brought on by social media. Another friend (probably a borderline genius, with a lot of medical knowledge as well) thought you made good points. He has a bunch of relatives that are ER doctors, and I bet he’ll spread the information further.
My biggest regret
I have 3 beautiful daughters. It breaks my heart that I didn’t know this until May 26, 2021 when I attended Dr. Bridle’s presentation to the CCCA. After the call, I spoke with Dr. Robert Malone and all the pieces to the puzzle dropped into place. The vaccine sets up shop in our daughter’s ovaries cranking out a dangerous spike protein for up to 48 hours that then can stay around for 30 days. What that has done to my daughters’ ability to have children is unknown at this point. I tried my best to get at least one repurposed drug to be approved by the NIH. But I was unsuccessful because of Tony Fauci, Cliff Lane, and the NIH COVID Guidelines committee inability to evaluate all the available evidence and use the Precautionary Principle to minimize loss of life. Only Congress has the power to end this; they enable Fauci and Lane.
I am PRO-VAX. Vaccines in general are good.
Vaccines are supposed to help people avoid disease.
Vaccines are NEVER supposed to kill people. There is always an associated death toll from vaccination, which combines adverse reactions to the vaccine (almost always not deadly) and background deaths (because people die all the time). For influenza, according to VAERS, it is less than 1 death per year for the 30-39 age group (fewer incidental deaths in this age group, so easier to see the number killed by the vaccine itself is close to zero).
When was the last time we had a vaccine that has killed over 20,000 people worldwide and disabled probably more than 200,000? Never.
I’ve never in my life seen a vaccine which has the devastating side effects as this one. Not even close. More than half of the adverse effects in VAERS are from these vaccines making them more danagerout than the 70 vaccines over 30 years combined.
Compare this to the flu vaccine which pretty much kills about 0 people per year (as demonstrated in this video). If this vaccine was as safe as the flu vaccine, I would not be writing this article. But this vaccine is dangerous: it kills and maims people in unpredictable ways. People go in healthy and come out dead or disabled.
President Biden wants to move forward aggressively to vaccinate more people.
Biden, CDC, FDA should call a STOP to this now until we know exactly how many people have been killed and/or disabled.
Promoting repurposed drug protocols and educating people to treat as early as possible (even before test results come back) is a safer and more effective approach that can reduce the absolute death toll to a fraction of those killed every year by the flu.
The censorship of patients and doctors is both troubling and unprecedented. Why are doctors threatened with loss of license for raising legitimate concerns? If the vaccine is as safe as they claim, why do we need to muzzzle doctors?
The reason a doctor or scientist isn’t writing this article is simple: fear of retribution. You would never get another NIH grant in your career or ever get a drug approved by the FDA.
The lack of transparency is troubling. Nobody will say how many people have been killed by this vaccine. We know it is at least 4,200 in the US alone but is likely much higher. The V-SAFE database is hidden from public view.
How can a vaccine that has killed at least 20,000 people worldwide so far this year be mandatory, yet ivermectin which has killed less than 16 people over the past 30 years (and it’s probably zero because the associations are never 100% accurate) is considered too risky to recommend for COVID despite 22 published positive studies (for early treatment). That’s baffling.
The long term consequences of these vaccines are unknown. We should know these before we inject healthy young adults.
There are viable alternatives with a better risk-reward profile such as early treatment or waiting for the Novavax, Covaxin, or Valneva vaccines. The Valneva vaccine is expected to be variant proof and uses tried and tested vaccine technology.
The most important thing is to educate yourself on the potential benefits and risks of your options, talk with your doctor, and jointly make the decision that is best for you.
You can always wait to be vaccinated, but you can never be unvaccinated.
If you enjoyed reading this article, please follow me on Twitter at @stkirsch so I can keep you apprised of how this story progresses and what you can do to help. You can DM me suggestions to the article but it is pretty long already.
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Steve Kirsch is a high-tech serial entrepreneur based in Silicon Valley. He has been a medical philanthropist for more than 20 years. When the pandemic started, he left his day job at M10 and started the COVID-19 Early Treatment Fund (CETF) which funds researchers from all over the world running outpatient clinical trials on repurposed drugs. CETF funded David Boulware’s trials on hydroxychloroquine and the Phase 2 and Phase 3 fluvoxamine trials, among many other research projects. He was recently featured on 60 Minutes which highlighted his work with fluvoxamine. He has no conflicts of interest; his objective is to help save lives. In 2003, Hillary Clinton presented him with a National Caring Award. He wrote this article to share some of what he has learned over the past year about the failure of evidence-based medicine during a pandemic in the hopes that people will realize their mistakes and change their views.
Note that views expressed in this opinion article are the writer’s personal views and not necessarily those of TrialSite, Inc. or the COVID-19 Early Treatment Fund.
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