24 Comments
Mar 8, 2022Liked by Jessica Rose

I know humans benefit from this research, but it still makes me sick what we do to these poor test animals.

Expand full comment
author

i completely agree.

Expand full comment

Define" benefit" given these results of the toxicity and organ concentration of the lipid (NLP) mRNA covering-- never used before.

Expand full comment

Agree with that. I was referring to medicines in general.

Expand full comment

Indeed it is quite fascinating (not in the good way) that this study was done after the vaccines had been injected into the first human test subjects. Here is another interesting read on that paper: https://moderndiscontent.substack.com/p/more-on-biontechs-lipid-nanoparticle?s=r

Thank you for the tremendous work you are doing. When your eyes have been opened to what’s going on there’s no going back …

Expand full comment

Such findings should have resulted in the immediate discontinuation of Warp Speed.

Expand full comment

Amen to that! Their claim that the “vaccine never leaves the site of injection” is a blatant lie.

Expand full comment

Yup 6- 8 hours after jabbed its in the liver and looks like the ovaries-- where else?

Expand full comment

The most telling thing about this data dump so far for me is, I duckduckgo "Phizer data revelations" and "Phizer data dump" and not one single article from any "legitimate" news source pops up, like it is lost in a deliberate legacy media blackout. That confirms for me my thinking that this war was provoked by the same forces who can impose upon the media such uniformity around Covid Policy.

Expand full comment

I am disgusted for humans and animals that this disgusting business if even a thing. Makes me want to vomit at how inherently evil human beings are that we would do any of this and then, with the results these products had on the rats, put this garbage into humans.

Expand full comment

It might be helpful to also look at the nonclinical evaluation report that was submitted to the Australian authorities. It is discussed by Dr. Mikolaj Raszek (merogenomics) in his vlog, in which he also notes that one of the figures inadvertently shows that the spike protein can be seen in the nucleus of transfected HEK cells. See https://www.youtube.com/watch?v=WmeWdc6-mwg&t=146s

Expand full comment

good god

Expand full comment

Well those rats didn't play ball so on to the humans then!

Expand full comment
author

poor rats didn't stand a chance :(

Expand full comment

I'll never talk bad of a rat ever again!!

Expand full comment

After reading this you come to a clear objective answer in ones head. Vaccine was not ready for hey day!

You are a great data scientist. Not trying to flatter you just simple observation.

Expand full comment

I have been down the rabbit hole over the past few days after reading about some anonymous moderna whistleblowers (probably) who claimed in 2020 that the vax was actually intended to hit the liver and ovaries and do a few other strange things as well.

All crazy, except that the evidence seems to be accumulating in their favor over time.

https://igorchudov.substack.com/p/steve-kirsch-germ-line-mutation-allegations

These substack guys want to prove that this isn't the case (because if it is, we're screwed) and would appreciate any advice or opinions about how to do it, I'm sure.

Expand full comment

I should add the allegations, which very notably discuss the liver and gonads. This was before the Japan leak, I believe.:

I'm an industrial engineer at Moderna and the other one of us is a process development engineer. I'm sure the same thing is happening with Pfizer-BioNTech. It was hard to put things together based on the small quantities of additions happening in manual step (highly unorthodox for a continuous process production). The explanation we got was highly sensitive trade secret adjuvants being added. Digging in deeper showed how sensitive it actually was.

Most people's understanding of this novel vaccine type is that it works as follows:

Make mRNA coding for S protein

Make lipid nanoparticle delivery system

Profit

How it actually works from what we've uncovered:

Make mRNA coding for S protein

Make mRNA coding for mutant versions of CYP19A1 and CDKN1B in smaller amounts

Make sure that while delivery system for (1) mostly ends up in liver, most of (2) ends up in the gonads

Make sure form and quantity of additive upregulating LINE-1 reverse transcription activity makes it hard to detect among legit adjuvants

Effects from (2) integrated by (4) are recessive; mildly oncogenic effects in vaccine recipients unlikely to be noticed for many years

(5) recessive but since most of population vaccinated, in next generation female offspring have premature ovarian failure

Expand full comment

I wonder if the high dose distribution peaks higher and clears faster than the lower doses which rise more steadily over time, giving similar area under the curve (AUC) overall. Do you have a hypothesis for the gender differences in distribution patterns? Could it be related to tissue partition coefficients and body fat distribution?

Expand full comment

Thanks for reading through this data dump and making these charts. Women have smaller livers than men as we all know from the fact that men can hold their liquor better. I've heard that this hits the women the hardest.

Expand full comment

That seems to be confirmed in the Pfizer Post-Marketing Experience document 5.3.6 - women have more severe adverse effects of certain types.

Expand full comment

I'm also wondering how protein binding affects the distribution. From the Nonclinical Evaluation Report:

"Major findings

 Plasma concentrations of ALC-0159 and ALC-0315 decreased rapidly (initial t½ of 1.74 and 1.62

h, respectively). ALC-0159 and ALC-0315 were slowly cleared from plasma, with terminal

elimination t½ of 72.7h and 139h, respectively. AUClast was 98.6 μg.h/mL for ALC-0159 and 1020

μg.h/mL for ALC-0315, and AUCinf 99.2 and 1030 μg.h/mL, respectively (Figure 4-1).

 ALC-0159 and ALC-0315 concentrations in plasma dropped 8000 and 7000 fold, and in liver >

250 and 4 fold, respectively, 2 weeks after dosing.

 The liver appears to be the major site of uptake of both lipids from the blood (~ 20% of dose for

ALC-0159 and ~60% of dose for ALC-0315 (based on the highest mean amount at 1 h and 24 h,

respectively). Faecal excretion of unchanged lipids was ~47% and ~1% of dose for ALC-0159

and ALC-0315, respectively (Figure 4-2). Both lipids were below LOQ in urine."

Expand full comment

Considering the higher uptake in liver, spleen, and adrenals - and the adrenals control blood pressure and electrolyte balance - can we hypothesize that electrolytes are so off balanced that they could cause heart arrhythmias, kidney issues, nero problems? If your constantly dehydrated your screwed! In my experience I am having a very hard time staying hydrated no matter my input. Noticed this early on after my pokes (work initiated). After I read this my “ding ding ding” alerts went off about adrenal and liver. My digestion has been very bizarre. Anyway, thanks for all you do JR 🌹 Are electrolyte panels standard with blood testing?

Expand full comment