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Inflamed_Heart_Liberal


				

				

				
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joined 2022 September 05 17:30:11 UTC

				

User ID: 648

Inflamed_Heart_Liberal


				
				
				

				
1 follower   follows 0 users   joined 2022 September 05 17:30:11 UTC

					

No bio...


					

User ID: 648

Yes, the evidence is the nature of how effective natural immunity is compared to the vaccine induced immunity, which wanes. You will receive the protection of the vaccine, and more, if you get natural immunity, therefore your next encounter will have a reduced magnitude compared than if you had just the vaccine alone.

I feel like you're fishing for exact, quantitative data - I need you to be patient as data about our current times is collected. I'll have evidence to back up thr natural immunity claim in the future, just like we saw develop in 2020-2022. This is a developing emergency, that the vaccine has had some malfunction / additional risks of heart problems that are only being discovered recently. I wish I had the long term data of our developing vaccine emergency NOW, but that's simply not an option. I'm happy you agree with my overall hypothesis though.

Any procedure is a minor procedure if its not being done on you. Ibuprofen CANNOT cause you to show ECG changes and have your heart puke out troponin

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How do you think conventional vaccines make it to your lymph nodes? Both mRNA and conventional vaccines transit from the site of vaccination to your lymphoid organs via blood/lymph.

Again, lymph vessels are more like one way valves. Yes, mRNA "pre-vaccine," and conventional "already-completed and molecularly confirmed" vaccine, are moved into your blood stream. Why are you bragging that unconverted genetic material gets a lift in the blood stream? That is aboslutley not the goal here. Lymphatic absorption is what we're dealing with.

The centuries of science around conventional vaccines in the ages before we knew what B/T cells were probably don't count for much, and I doubt the live cowpox vaccines that you'd prefer had fantastic safety profiles.

Extremely anachronistic view of medical science. Dodges the gap in genomics that these vaccines depend on. Thinking now of the 2060 version of us looking at the first generation lipid nanoparticle mRNA that people took. Talk about prototype!

It was pulled because both the safety profile and efficacy were worse. And of course it's a fallacy, on par with people have always dumped raw sewage in the Thames and cholera is just a fact of life. There's strong data that the mRNA-vaccines are safer and better than J&J or other non-mRNA vaccines developed abroad, unless you put a huge premium on living 'naturally.'

The efficacy collapsed just like the mRNA vaccines, this is why you're on dose number 5, and defending data from dose number 3. You have introduced an entirely new set of dynamics to your immune system, one that those who receive conventional vaccines will not be exposed to. You have RNA transfective particles leaking into your blood stream, while I do not. Guess the fallacy does much better with actually winnable man made advancements in public health.

I'm out of characters, but note that antigens are also 'conjured' at the ribosome with your viral vectors, and the other vaccines you refere

My final statement: mRNA leaks into blood stream, J&J does not. This is a problem beyond the normal vein of risk-benefit analysis. This is malfunction analysis.

Inflammation from widely distributed nanoparticles. Look up inflammation, its complicated.

Novavax is a novel virus-like particle. I personally would much prefer Novavax over mRNA, and probably over adenovirus vectors.

I just don't like the threat of heart problems that mRNA presents. Such a large, dark downside to the products, to remodel your heart.

Everyone in the myocarditis study was not a young male. It just proves, that sudden death after vaccination can be downstream from the very "well understood" and "mild" myocarditis that the vaccine is associated with.

You are tricking out old Covid morbidity statistics against your best possible analysis of mRNA. For the right age group, you could see a 1 in 2,000 risk of heart damage.

Anyone who's heart stops after vaccination, could have died from the vaccine. The vaccinators did not study the vaccine long enough to even know this until part-way through the campaign, when it became "a known issue that doesn't hold up."

A lot of people had investment in mRNA stopping transmission, and that was why this rare side effect of "some heart damage to young people" was being hand waved. During the "we are getting herd immunity phase," It seemed like you would accept any risk to young patients to stop community spread. That's concept has collapsed, and you're trying to say that the vaccine is only somewhat as deadly as the disease you are actually trying to vaccinate against!

5 per 100k, 150 in 100k. Think of ALL the unreported covid cases that were mild or asymptomatic. You are showing me the best possible rate of myocarditis, and it holds up next to a disease. That's not great vaccine, even if you think an 85 year old in 2020 should have obviously received it (and then it wore off by mid 2021).

Thanks. I read all your comments.

You are detecting partisanship, as well as someone who was mandated. This is a huge deal for me. I cannot thank you enough for engaging me, it's extremely difficult to find people to debunk my own thought etc. I think you make a lot of good points and it will help me moderate as I look forward to further evidence.

I think some developments are going to vindicate me in the future, and a lot of your objections are well placed to defuse my ability to make claims at this current time. Until then, I unfortunately am bubbling with some vitriol.

Opinions I cannot prove to you the way you'd like:

Covid is safer than they can possible report.

The vaccine is more dangerous than they can ever possibly report.

Maybe take a gander:

This study finds a 1 in 100,000 death rate for the vaccine.

https://www.nature.com/articles/s41467-022-35653-z

Thought it was interesting, if you have not yet seen. Thanks again and have a good one.

There is no experimental research finding heart damage in cadavers after receiving ibuprofen. Only mRNA. Not terrifying to me.

My eyes on this for sure. It makes sense that a vaccine vector that can enter the blood stream and deploy (mRNA nanolipid) is acting like an allergy shot.

I agree. We cannot pull any amazing anti-mRNA vax narratives from this, but we can agree that discovering unexpected changes in the antibody profile is of interest. My first thought was literally, excuse my levity, that this is "cringe."

Inaccurate. If you look at the mRNA vaccines in particular, they can cause a heart condition that can cause death. Its a well recognized condition called peri-myocarditis. Are those deaths worth protection from covid? That's the argument that's falling apart right now.

"Lingering effects of novel viral illnesses have been well-documented" Did you mean to use the word novel? There are lingering effects possible of all viral illnesses, not just novel ones. I would not compare this to Spanish Flu, compare it to The Russian Flu/Corona of 1800s..

The idea that nascent respiratory infection would have killed someone that had a "mild" reaction to the mRNA is completely unsupported, and conveniently forgets the introduction of the novel nanolipid particle that delivered this first generation vaccine.

https://pubmed.ncbi.nlm.nih.gov/36436002/

So the vaccine can make you die in a special way due to lymphocytes in your heart - but the idea that Damar did not have any type of underlying structural sensitivity to a tackle is completely debunked...I do not think so.

This is not the right take.

You should be much more concerned about the size, shape, and ability to move through your body compartments with a Vaccine, than with a virus entering your mucosa.

The virus, if anything, is very limited by ACE2 receptors, whereas the lipid nature of the mRNA droplet allows it to merge into literally any cell and make it into an antigen producing cell. Much more than ACE2

https://pubmed.ncbi.nlm.nih.gov/36436002/

Why are hearts found with heart damage in cadavers? Why is it not plausible that this is a actual issue?

The online right is, alternatively, demonstrating the exact appropriate amount of interest you'd expect, countering the efforts of a public health campaign to minimize this information.

This is a strong candidate for a contributing factor to deaths. For example, I'd argue that loss of job due to a vaccine mandate will carry worse outcomes than actually receiving a vaccine, or getting Covid unvaccinated. So in a way, our own public health response could be responsible for causing harm to people

This is not all proven - the vaccine entering body tissues because there's no known characterization of nanolipid particle pharmacokinetics is the main issue her. There's no concentrated ACE2 receptor in testicles, but the nanolipid particle will be exposed to the testicles via the blood stream (at the testicle blood barrier, which the vaccine can cross).

That hardly explains why the same lymphocytes at the deltoid vaccine site were found in the cardiac tissue. It was a specific immune related reaction.

The vaccines are dangerous precisely because we are analyzing and looking for hidden harm, after we already administered a billion doses without fully understanding the consequences and outcomes.

mRNA cardiovascular toxicity is a severe problem and if it's at all likely, the hammer should drop. This "blip" is an 18 year old about to get mandated with mRNA bivalents before going to a community college.

Also, we have tons and tons of data on "coronaviruses", and SARS 2 is one of those. mRNA nanolipid particle injections? Less experience, to say the least.

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Yes. Let's begin. I apologize for my lack of formatting, you're right, it was meandering.

Be careful drawing facile conclusions from large correlational studies like this. And not to be a paternalistic douchebag (feel free to ignore if you know better) but you might find it helpful to skim the discussion of a paper if you aren't familiar with the field to at least get a feel for the limitations or alternative explanations of the study.

Yes, there is a complete heterogeneity of the population at this point. I understand the point, and I appreciate you walking through more of the PE risk benefit. I am relatively familiar but didn't enter the weeds. I agree this is a correlational study. I am aware of the authors explanations and limitation.

They are forced to use historical data.

They are forced to use the worst possible CFRs when we had the least tests available and the fewest eyes on the spread, compared to a disinterested, uninformed group of clinicians who would have been responsible or detecting vaccine side effects. We need pathophysiological studies and autopsies - once again extreme lack of interest in autopsy for vaccine recipients. The data is muddled, so we need firm exploration into underlying mechanisms and gaps in our understanding of mRNA vaccines.

Let's look at other studies that show problems with mRNA. I can't link them to PE myself, you need to take your pathophysiology knowledge with you into this exploration.

There is a suspicious group of studies that cast extreme doubt on the basic functioning of the mRNA vaccine as an antigen producing unit that remains in the deltoid.

Usually sudden death after vaccination would be related to anaphylaxis due to an allergy to some vaccine component, whereas the myocarditis takes a few days to develop.

First, in my healthcare facility, Anaphylaxis was less than double the increase from traditional vaccines. I would say mRNA performed very well in the realm of anaphylaxis (remember, allergic reaction 2 body systems and life threatening). I have suspicion that mRNA is responsible for allergic generation issues (e.g. anecdotal bilateral hives after vaccination) but I have no evidence. I just know that mRNA spreads its antigen creating goodness throughout the body, at a frightenly common rate. If you see sudden death as a possibility of anaphylaxis, you may be mistaken in some ways.

I am surprised you are unfamiliar with https://pubmed.ncbi.nlm.nih.gov/36436002/, Autopsy-based histopathological characterization of myocarditis after anti-SARS-CoV-2-vaccination.

Note lymphocytic infiltration of cardiac myocytes (I won't even continue on with the arrhythmogenic implications of this permeant heart damage, a.k.a. died suddenly). Yes, vaccines are supposed to enter your lymph and lymph node, but your lipid nanoparticle has different pharmacokinetics, and seems to pass the lymph nodes and enter your blood stream, whereas my J&J virus does not. This is a huge win for me, over your choice of vaccine. Let's see - deltoid goes to lymph vessel, lymph vessels carry mRNA to lymph node, some of the trillions of mRNA baubles awash past the lymph nodes and get dumped into venous circulation (right before entering the Right Atrium of the heart). This is all done before even getting a pass at the liver.

Yes, I think a bad football tackle can exacerbate the exact underlying pathology that was discovered in the German Pathology Autopsy reports. Entirely plausible.

J&J has a form of tropism to enter cells, wheras mRNA is enclosed in a non-tropic lipid droplet that can fuse with the phospholipid bilayer of much more than just a muscle cell. Lymph vessels are a one way valve that do not require deposition of mRNA payload to enter lymph circulation (then subsequence blood stream circulation.

Did you know the lymph is responsible for distributing dietary lipids to your blood stream? Are you concerned that you took a novel lipid and entered it into the system that transports macronutrients? The early applications of lipid nanoparticles were as oral form blood pressure medication. Why? The lipid nanoparticle is great as distributed systemic effectors. Your vaccine distributed mRNA as if it was a beta blocker.

The mRNA vaccine is found in breast milk: https://jamanetwork.com/journals/jamapediatrics/fullarticle/2796427. mRNA enters the blood stream at a rate higher than other vaccines.

Spike protein is in blood stream of myocarditis patients. https://pubmed.ncbi.nlm.nih.gov/36597886/

I don't think spike protein is the issue, but the signal that the antigen is in the blood stream. What exact tissue was the antigen created? Probably not exclusively in the deltoid myocytes.

There's plenty of papers: Here's a review that will have a summary and a couple dozen primary references if you're interested. Many primary papers investigating the mechanisms as well.

Thank you. Looks like the etiology of blood clots from Covid related PE would be different from an mRNA related PE, so we need to be especially suspicious of the signal that the mRNA vaccines could cause a PE. Especially since historical data has to be used due to lack of long term safety monitoring before mass vaccination. If severe flu can cause PE, I'm extremely unmoved by severe covid causing PE. Viral pneumonia sucks and too bad antibodies can't hover inside of your parenchyma and actually generate a sterilizing immunity.

Since I will not be getting Covid Viral Pneumonia, I am very interested in the chance that this "routine medical procedure" can cause PE.

The last time I looked into myocarditis it was vanishingly rare, a tiny number of deaths were attributable to it and those individuals seemed to have many other medical conditions.

the authors report zero deaths associated with vaccine-induced myocarditis

This is a horrible sign for your data, since I've seen the slides of lymphocyte aggregation in the deltoid of a cadaver, as well as in the heart of a cadaver after vaccination. What do you think of this discrepancy? This is an 11 month old reddit post, the autopsies were not completed then. I think it makes your data look unusable. As a counter to the redditor - maybe this is CIA propaganda to make the vaccine seem safe, to counter Russians propaganda to make you think the vaccine can kill you (which the Germans actually proved was true). This was all in the reddit post you linked to - not an unrelated sneer.

https://onlinelibrary.wiley.com/doi/full/10.1111/eci.13947

Yeah admitted self own, this is the Prasad paper, which paints a stratified risk that is not vanishingly rare. I'm not pushing this more than my above point.

As well say this for tetanus, flu, rabies or any of the other viruses we need boosters for. Immunity wanes particularly quickly for respiratory viruses. Note also that the Moderna booster is a half dose, so modulo some weird memory effects likely has lower rates of adverse events.

Come on. None of those vaccines involve mRNA lipid nanoparticles. Getting boosted with mRNA to seek antibody titers is aboslutely not the same thing as getting a tetanus booster in 10 years.

I mean this is a very very polite way - how did you find your way to the Motte? You started strong, but these are common misdirections on the exact argument - mRNA is a special novel biotechnology, stop mentioning vaccines that the market overwhelmingly accepted, and has centuries of application in the exact antigen deliver method (protein adjuvant). Have you ever mix and matched a measles vaccines in a year? Even when no data existed on it? Pfizer admitted you should not mix and match Comirnaty because of lack of data, you can only mix and match the EUA product. Which is...something...

I don't think we know the risk of myocarditis after reinfection; it's almost certainly lower, but I could only find two case reports so it's difficult to draw any conclusions or calculate the relative benefit of vaccination. Moreover, tens of thousands of elderly patients die of flu every year, and I can guarantee you that they aren't immunologically naive. Natural immunity isn't a silver bullet.

Okay, you agree with me, its certainty lower. Yes, I think it would be nice to distribute vaccines to elderly patients who are vulnerable. Is this why the FDA is vaccinating pediatrics? This is just a vacuous talking point. You just called Covid a flu. Why would you get the experimental nanoparticle for "just a flu bro."

I'm not sure I understand your point here.

It was not really for you. You seem to get it.

That being said, we've been infected by influenza for at least 1,500 years and it's still a major public health concern. A truly protective vaccine would be a major coup, and investing resources in these problems is worthwhile even if lockdowns and mask mandates are not.

Yes, more evidence that the entry of a novel, circulating respiratory pathogen into the population that targets elderly and vulnerable is entirely normal, see the Russian Flu in the 1800s. What's not normal, is becoming a fanatic for biotechnology.

The calculus for the vaccines was just much better early in the pandemic.

The calculus was "seek herd immunity." This involved minimizing the collapsed efficacy of the vaccine mid-distribution. Once again, you love comparing every known vaccine dose to every known covid case, when we absolutely know there is more infection than can be reported into the data. Then "severe disease and death."

My calculus is: the vaccine leaks into your bloodstream, and seeking protection from severe disease and death from one respiratory pathogen with a vaccine that leaks into your bloodstream is not advisable.

No there's a meaningful legal, judicial, and regulatory framework surrounding those vials. And the public health vaccination campaign.

Among the 35 cases of the University of Heidelberg, autopsies revealed other causes of death (due to pre-existing illnesses) in 10 patients (Supplementary Table 1). Hence, these were excluded from further analysis. Cardiac autopsy findings consistent with (epi-)myocarditis were found in five cases of the remaining 25 bodies found unexpectedly dead at home within 20 days following SARS-CoV-2 vaccination.

5/25

Well, this is not the statistical smoking gun I want per say.

So of 35 sudden deaths, 10 were other causes. And then of 25 sudden deaths, 5 were found to have thee abnormality. They were looking for sudden deaths from myocarditis and they found it.

Who knows. We basically agree in a bunch of domains, I just think it's still not possible to say this is a disproportionally unimportant issue.

https://youtube.com/watch?v=j_DdSMn55cA&ab_channel=Dr.JohnCampbell

Here's Mr. Campbells exploration. If you're looking for more.

Most of my vitriol came from my education. I've been wear of mRNA since summer 2020 when it was announced as a candidate. I've taken undergraduate STEM, but most importantly, I worked with "science and technology studies," where we looked into a century of scientific ethical dilemmas.

So many people got the vaccine when they were told it would stop transmission - I had read the original clinical paper, and saw this was a messy conclusion. Then data from Israel came out that protection was waning, then the censorship began, and later on the mandating piggy backed on the censorship of waning efficacy.

I guess that was part of the show. Vaccines were already so safe and bullet proof, people cannot notice when one that's 10x dangerous is released, and information censored online, and physicians told to be disinterested.