Pediatric RSV vaccine trial enrollment on hold
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FDA pulls vaxx product, after its trial is a disaster.
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clinical trial for RSV, Respiratory Syncytial Virus, in kids
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unvaxxed group had only 1 case and it wasn't serious, kid was fine
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while in vaxx group, 5 kids had to be hospitalized - for RSV. infant nearly died
That's the news. Now to explain it.
Why would vaxx group be worse off?
First: RSV - like covid, flu & HIV - is single-strand RNA virus.
RNA viruses evolve fast. Vaxxing them, over-trains your body to fight old versions, while virus itself moves on to new versions, that specially exploit over-trained people.
This is why flu & covid vaxxes seem to attract infection, or make you more likely to get sick - Fauci had his 3rd covid infection after his 4th booster shot - and why there is no HIV vaccine.
In technical terms, vaxxing for RNA-type disease can have a number of bad effects, variously called
- "immune escape" or "antigenic escape"
- "immune imprinting" or "original antigenic sin"
- "antibody dependent enhancement".
Big Pharma, FDA & CDC know all this - or should - but there is big money$$$ in covid & flu vaxx.
For flu & covid, they shove vaxx products out the door, even though they can never quite work & may leave you worse off.
It's a miracle that, for some reason, when it comes to RSV & HIV vaxx products, they don't.
Second: The new technology in particular, mRNA + LPN (lipid nanoparticle), may cause side effects in some unlucky people.
With this technology, in some unlucky people, vaxx escapes the injection site & hits rest of your body. It can wreak havoc in cells of vital organs.
For covid vaxx, this second group of bad effects may show up as vaxx-induced heart disease, blood clots, auto-immune diseases, etc.
If you like your news in video form:
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ps. Third, depending on company & product lot: the mRNA-LPN may be contaminated with weird, inappropriate DNA fragments (toxins) from RNA manufacturing process.
It's been proven that the product lots which show up for injection into people, are different & sometimes more contaminated than the nice clean product lots which that company sent in for government approval.
Pfizer was nailed last month:
We...identified large amounts of DNA after RNase A digestion in all lots with concentrations ranging from 32.7 ng to 43.4 ng per clinical dose. This far exceeds the maximal acceptable concentration of 10 ng per clinical dose that has been set by international regulatory authorities...including the SV40 promoter/enhancer
"SV40 promoter/enhancer" means: contamination that will cause cancer.
Do not assume other companies are better.
BUT, this factor applies to mRNA vaxx in mass production (covid). For RSV clinical trial (thread topic), company probably sent in clean lots. So, RSV trial problems would be the other problems, stated earlier.
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Referenced by B blablarg18