Inflamed_Heart_Liberal
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User ID: 648
Inflammation from widely distributed nanoparticles. Look up inflammation, its complicated.
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.
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.
Agree with this.
I think Omicron is a large narrative tool.
Omicron is so much more deadlier than Delta because of its transmissibility, but this translates to less threat to each individual. I always grin when I see people "celebrating" omicrons rise, or remark how they avoided nastier variants, and now play host to the most transmissible pathogen in recent years. If you can catch a cold, once again, that means a 90 year old in a nursing home can catch it too.
Thanks for coming in and adding your input. I would note to all readers that Chrisprattalpha and I had a more detailed vaccine back-and-forth that I thought was productive. Mr. Alpha linked to it in his post.
Overall I disagree with the idea of the "very safe" label. People should go look at our previous exchange to see where I disagree.
As for the vaccines, if they don't update them I'm not planning to bother unless forced to by my employer.
Well, once conventional vaccine alternatives are available to "tic" the box, I would much rather choose protein adjuvanted injections over job loss.
I have not been exposed to mRNA, so it makes a lot more sense for someone like me to be choosier, rather than someone who has taken a more novel method of vaccination.
And we're all getting Covid-19.
Yes. Imagine someone saying "Let's try injecting the antigens into their heart!"
Well, we know the mRNA enters the bloodstream, so it could transfect any cell...
Well, the carbohydrates will not fold into a protein. Carbohydrates mainly going to enter the blood stream as glucose, simple principle of digestion and metabolism in human physiuology.
Using your muscle cells, vs. using one of your cardiac muscle cells, is why you do not want mRNA droplets in your blood stream interacting non-specifically with your organs
People entering the medical system and producing positive incidental Covid-19 infections are already likely to be sick.
"It was based upon nearly 154,000 patients with Covid (median age 60, 90% male)"
How can this be related to a 21 year olds decision to avoid getting a mRNA vaccine, known to have cardiac side effects, when the study looks at an already unhealthy patient population?
Not even trying anymore, Mr. Topol may be right that Covid causes problems, but his whole basis reeks of damage control.
The vaccines, with their side effects, need a deadly disease to be worthwhile giving. We are riding out the last days of accepting a chance of heart damage to be immunized against a contagious disease that you get exposed to at the bar, grocery store, and in your home.
Your response didn't address the crux of FDA and EUA labelling. The entire power structure of our country, legal recourse and all, rests along these lines. Sorry to bring Foucault into the mix, but he's the ultimate nightmare of a public health pandemicist.
There are no data available on the interchangeability of COMIRNATY with COVID-19 vaccines from other manufacturers to complete the vaccination primary series. Individuals who have received 1 dose of COMIRNATY should receive a second dose of COMIRNATY to complete the vaccination series.
Is this not VERY different from the medical advice given to people getting the EUA? Mix and match the first vial you can even get your hands on?
1 in one million, compared to 1 in 100,000, in our current data collection environment, is a good signal to keep track of if you are considering your options to receive a covid-19 vaccine. Perhaps you can take J&J, Novavax, or Covaxin and maintain protection against SARS-2.
The IFR is lower and vaccines are not denting hospitalization or death rates as they plummet from their previous heights (mass naïve infection). Most people have had a much better inoculation than a monovalent vaccine - they've had a SARS-2 infection.
Do you plan on explaining why or are you just going to make assertions?
Well, because a stroke as a cardiovascular event, I'm interested in the dynamic between mRNA vaccination and your cardiovascular system. A stroke, downstream of pathology, will offer valuable information when it goes above the baseline.
It's entirely possible to build towns and cities that don't require you to drive literally everywhere....A minuscule improvement in civil design would save orders of magnitude more lives than eliminating all risk from vaccines, with lots of other positive side effects to boot.
Well, you are demanding rigor, and yet I feel like this is a complex claim. Even a city would involve having people driving to bring supplies and transportation towards these centers - a mandatory risk.
We should be paving our public serology with only the best, most well understood vaccines that we are capable of developing and testing and passing on in our limited lifetimes. There is a broader umbrella of rigor that I am requesting to be frank.
A lot of the rigor I'm demanding will also take time, more time than has been allotted for these Bivalent updates. The first injectable, multi-transcriptional (unknown if combined or separated) mRNA vaccine to market has shown an unexpected safety signal.
It's an EUA vaccine approved for an emergency. I think if you want to say "legitimately safe vaccine," it would be easier if Pfizer or Moderna could actually distribute an FDA approved and LABELLED as approved "Comirnaty" or "Spikevax" vial of vaccine.
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.
I would take another look at the study. There was cellular evidence that these cadavers could have had a dysrhythmia from the mRNA associated lymphocyte aggregation in the myocardial tissue. Not causal but pretty convincing.
Understood - I felt like it was wrong. I was blocked by aaa, I'm assuming because it was inconvenient to his argument or annoying.
I still find it odd that people skip over like this study doesn't exist, as it keep bubbling into all these tertiary debates about the possibility of vaccine sudden death.
Feels like an influx of a persuasion hit the board. Which I welcome, frankly.
Stopping immediately.
https://pubmed.ncbi.nlm.nih.gov/36436002/
Take a look at this autospy report. If you can find bodies that have died after vaccination, you can propose that people are dying after vaccination, from the vaccination. I find it bewildering that people are uninterested in the long view of isolated cases of heart damage, and a novel biotechnology vaccine (that could be substituted for a conventional vaccine at that!).
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.
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
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."
(2/2)
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.
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
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).
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.
Did you know most people who get divorced, will get remarried?
The overall picture is that stability has crashed. Also, I hope you learned your lesson / enjoyed the reminder about blue vs red state demographics..
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