This is NOT medical or scientific advice. It’s the thoughts, opinions and ideas of an Average Dumb Guy. Do not quote them, do not use them in any case or argument. Use them to do more research or generate new ideas….
They are here for anyone who wants to look for rainbows in this mess, or to use for further investigation.
All the data that scientists are studying is using the “purity” of the Wuhan 1 sequence (Spike). It is very clear to me, that YOU DO NOT WANT PURITY WUHAN 1 SEQUENCE being injected into your body at ANY COST! The research being shown with PURITY SPIKE COULD PROVE TO BE A NIGHTMARE for the unfortunate ones that did receive a “functional dose” of the spike-based therapy. It also makes ZERO SENSE to me to use Wuhan 1, as it went extinct a very long time ago.
Side Note: You cannot vaccinate for a coronavirus! But this is a whole other conversation.
I believe that ALLOT of people did not get a complete product in the early stages of this mess.
What is being delivered now can and is probably a very different issue though. There has been much time to refine processes and ensure proper manufacturing potential and to deliver a PURITY OF SPIKE. However, NONE of this can or has been confirmed.
So, if you have “dodged your bullet”, even if you haven’t and ARE SUFFERING FROM A THERAPY INJURY. I would say do not take any more!
Especially when considering the REAL RISK attached to SARS2 infection.
If your Infection Fatality Rate is anything above the values below, then you need to ask your Governments and their Corona Advisory Boards what they did wrong to make yours above the Global value.
“Across 31 systematically identified national seroprevalence studies in the pre-vaccination era, the median infection fatality rate of COVID-19 was estimated to be 0.035% for people aged 0-59 years people and 0.095% for those aged 0-69 years.
*The median IFR was 0.0003% at 0-19 years, 0.003% at 20-29 years, 0.011% at 30-39 years, 0.035% at 40-49 years, 0.129% at 50-59 years, and 0.501% at 60-69 years.”
https://www.medrxiv.org/content/10.1101/2022.10.11.22280963v1
But back to why I believe MANY HAVE DOGED A BULLET!
mRNA genetic therapies as produced by Pfizer are one of the most sensitive products to ever be used
they need to be stored between -60C & -80C
when they are thawed and used for ppl, they need to be kept between 2C and 8C
Once thawed and taken into syringe they have only a few hours before being degraded and useless
These requirements we will assume were drawn up and confirmed via a laboratory setting. The place where all the studies take place
There is a very real disruption in the ramp up from laboratory (a precisely controlled environment) to real world
It is common knowledge that at the beginning of the vaccination campaign massive problems were being experienced in getting lab product into VIABLE mass production product
Here are some numbers thrown together for your consideration
In 2021 Pfizer aimed at producing around 1 500 000 000 doses
Later that year their outlook was adjusted to produce at least 2 500 000 000 doses, hopefully 3 000 000 000
Their website as of today claims they have 11 manufacturing sites (I would guess there were FAR less in 2021)
So let use the full 11 sites to be VERY GENEROUS
2 500 000 000 doses
6 849 315 per day
622 655 a day at each of the current 11 sites (lets go best case scenario for them)
25 944 per hour per site
432 per minute per site
7 per second per site
This is ONLY looking at manufacturing, and excludes COLD storage, COLD transportation and Global Distribution issues. Also consider the COLD requirements of each Country they are sent to, each COLD storage site at the Country, the COLD transportation, COLD storage etc
These numbers are a REMARKABLE ACCOMPLISHMENT for any type of vaccine production, that was only authorised in the months before manufacture process took place (but let’s keep the 11 sites)
Now apply the VERY SENSITIVE NATURE OF LNP & RNA technology into this SUDDEN RAMPED UP MASS MANUFACTURING
How is it possible that they delivered a FUNCTIONAL PRODUCT?
Read this Sub stack by Jessica Rose, and then some of my ideas around the product
Here are some of my thoughts
When I first read the Protocol for a Healthcare Worker etc to actually put the jibby juice together, I saw trouble. The Pfizer insert basically says they take the empty vial with the RNA in it. Then add a precise amount of saline, then turn the vial upside down, add some more, turn it again slowly, add more etc. The very nature of the RNA is so delicate, if this process if done shoddy it can most probably cause issue.
the LNP is also very fragile and will be prone to cracking or degradation from fluctuations in temperature. So I would guess that even slight changes in the freezing temps could have an effect on LNP integrity. There was no advisory notice on how to properly thaw the batches out (well non that I could find so far i.e work in progress). As Jessica pointed out in her slides above, the LNP/RNA must be kept in storage of insanely freezing C's. How this was made possible for long transportation is a KEY as well. Then once the product is thawed, there is a small window for it to be given. Now I ask, how did they manage this with vaccine centres? They got hundreds of people some days, and hardly any on others.
I was looking at this from a South African context (where I live) and we have BLOODY HOT DAYS! So how did they keep the product in the "Goldie locks zone". My guess is they didn't. Many vaccine centres had many already prepared syringes waiting. Which means these stood for significant periods of time (and what Centre was kept at temperatures less than 8C while the prepared syringes sat on the table? The people in them would have left!).
There is also the fact that these could have been moved to and from the fridges to keep them cold. This could affect the product with the manner they were carried, and even the constant variation in temperatures could affect the LNP itself.
South Africa is “blessed” with Pfizer extending the Expiration Dates of the product twice, due to low uptake. This is an immediate flag of product degradation for me. Now add in the minus 60C storage (I DONT BELIEVE ANY VACCINE SITES HAD THIS CAPACITY and they used dry ice only) leading to mass degradation of the Product?
When they first said mRNA jabs, I was talking a Molecular Physicist I know, and she said that her and MANY other scientists were VERY SCEPTICAL that they could ever ramp up production to an Industrial Scale.
I read allot of reports on how they had struggled to keep the product functional at lab level. So how they got it to mass production must have been via the Virgin Marys intervention or something….?
There is the manufacturing process, where I am told they use two jets (at nano scale level) to “fire” LNP and RNA at each other. This will allow for MASSES of issues IMO from blank LNPs, to ones with multiple RNA in them, to damaged LNP, damaged RNA etc? The issue of the LNP aggregating in production is also something to look at?
I will take this further and suggest that this can and does happen in vial state as well. Each vial can have the 5 or so syringe loads of product vary greatly IMO
If LNP aggregate, then some syringe loads could have no to very little of the product. While others could carry all the product in one dose.
This is a potential mechanism for the "how bad is your batch" perhaps?
The fact that Pfizer etc also DONT WANT ANYONE examining their product indicates there are things to hide. The 50% allowance Jessica’s slides clearly point out to is also a MASS indicator of this? There is no QC and whistle blowers have spoken of blanked out windows and great secrecy at manufacture sites.
In the rush for Pharma to grab their chunk of the lucrative market share, it would not surprise me if they also simply sent out blanks.
Then when the intended recipient gets their dose, their bodies acidity levels will surely play an immediate role upon the LNP?...but the actual physiology of the recipient is the last area I will look at.
For me it’s what do we look for now that there is a massive chance they have / are injecting naked RNA (degraded or intact?) and possible degraded LNP into the body? Naked RNA could lead to cancers? The degraded LNP could still impact the immune function of the recipient? Will degraded LNP still carry an electric charge? What does degraded LNP do once injected? Will most go unharmed? Will those that did get injured heal?
THERE ARE SIMPLY TO MANY QUESTIONS, WITH SO LITTLE ANSWERS.
MAKES YOU UNDERSTAND WHY TRIALS OF AT LEAST 15 YEARS SHOULD HAVE BEEN CARRIED OUT ON THESE BEFORE THEY WERE ROLLED OUT TO THE PUBLIC.
There is really so much to consider, so just spit-balling here. This is a work in progress, and all subject to change over time. It’s here for us to throw a new perspective on the issue. And HOPEFULLY it will drive progress.
The DoD is in charge of the pharma contracts, the product manufacturers are military subcontractors, delivery to the pharmacies is managed by the military, and the shots are considered govt property until it's in the arm. Lots of opportunities to game the process, including the manufacture, then cold storage of the product years in advance.