Monkeypox Part 3 (Do NOT EVER get their Monkeypox/Smallpox Vaccine NO MATTER WHAT)

Inoculate your family and friends with information now, before the media gets to them. This is a shot that Tony Fauci himself said a few years ago had an unacceptably high risk ratio

BS”D

With G-d’s help, advance knowledge of our enemies’ plans can be lifesaving. With this in mind I bring you excerpts from two important articles you may not have seen yet.

Dr. Jessica Rose wrote about the monkeypox (really smallpox) vaccine: (The email length limit only allowed me to include pieces of her post. Her full article is linked at the end.)

“Jessica Rose@JesslovesMJK

“JYNNEOS... Kind of sounds like a dreamy place where indeterminate evil spirits live. I had never heard of myopericarditis until about a year and a half ago. Now, it's all the rage. Interesting the timing here. Just before we 'need' it. Funny that?”

“But first, what is JYNNEOS, you ask? Well, you’ll know soon enough! It’s new! (no it’s not) It’s going to save you from everything! (no it won’t) It’s safe! (safety data questionable - funny that - especially for people with health concerns) It’s not a smallpox vaccine in the experimental phase! (yes it is)”

Just to show how weird it is that the CDC was spending their time giving guidance for use of the SMALLPOX vaccine back in November, when smallpox was supposedly totally eradicated from the world:

Continuing with the data Dr. Jessica Rose presents on the smallpox vaccine:

“Please go the BLA Clinical Review Memorandum on the FDA website. You will see on page 1 that this is an application for a Biologics Licence for a product called JYNNEOS made by applicant Bavarian Nordic A/S for licensing of smallpox vaccines with “at Least 0.5 x 10^8 Infectious Units of Modified Vaccinia Ankara-BN (MVA-BN)”. Vaccinia virus is the well-known cow pox virus often used in (recombinant) vaccines. Vaccinia is also known to cause “certain complications and/or vaccine adverse effects occasionally arise” and, according to the people who want to promote the products, ~1/M people die from inoculation using vaccinia. That was before the COVID-19 injections however, and no one has any way to predict if these products may be counter-indicated, for whatever reason.

There are many redactions in this 209 page document. Never really understood the redaction thing; I mean, besides to respect a clinical trial participant’s privacy, for example, why would you do it? I suppose that considering we are pre-super-surveillance state, privacy probably isn’t really what these people are trying to protect, is it?

Read the following paragraph closely. It’s on page 189. Now, first of all, how is it that half of the world population probably knows what a frikkin’ troponin is in the first place? Could it be because of the frequency of reporting of massive elevations of troponins in clinical myocarditis cases diagnosed in temporal proximity to COVID-19 injections? Second of all, did the ‘applicant’ actually continue monitoring cardiac events as part of the post-marketing pharmacovigilance plan as recommended by the reviewer?

“As you saw in my Twitter post, it is recommended in the presentation given by Brett Peterson in “Clinical Guidance for the use of JYNNEOS”, that people get counseled on the potential risk of myopericarditis given ‘its uncertain aetiology associated with replication-competent monkeypox vaccines’. And what about the potential risk of you’ve sustained heart damage from the COVID-19 shots?

“There is at least one woman in the POX-MVA-005 trial with ongoing Cardiomyopathy that is ‘Possibly related’ in a very young woman who participated in the trial. Healthy, 28 years old. There’s also a 30 year-old male with myocardial infarction that was ‘Possibly related’ as well, that they claim has since ‘resolved’. By resolved, do you mean he died? I seriously have to ask.

https://www.fda.gov/media/131870/download. Page 150.

“I don’t expect you to read the whole page that follows here, but you should. ACAM2000 is a really unpleasant version of a smallpox vaccine. Basically. Here it is reported that 18.4% of participants in the trials involving POX-MVA-008 and POX-MVA-011 (both Bavarian Nordic Smallpox vaccines) showed post-vaccination elevation of troponin regardless of health status prior.

https://www.fda.gov/media/131870/download. Page 188.

“Below is a general table reporting “Treatment Emergent Unsolicited Adverse Event by System Organ Class in POX-MVA-013”. The thing that struck me here are the high rates of infections and infestations in all study groups. What’s with that? Are we talking Shingles here? Scabies? What? Since 9% of people in one of the study groups (Group 2) may have suffered a Shingles outbreak, for example, then that’s worth reporting on. Shingles is serious, contagious and horribly painful. And highly associated with the COVID-19 shots. Ahem.

https://www.fda.gov/media/131870/download. Page 116.

Why did they redact the number of days since last vaccine for the Fetal death report here? And what do they mean by ‘Resolved’?

https://www.fda.gov/media/131870/download. Page 123.

And they did it in every spontaneous abortion case and foetal death case but for no other Severe Adverse Event (SAE). Why?

https://www.fda.gov/media/131870/download. Page 125.

My guess would be that they didn’t want anyone to know the short temporal distance between the injection and abortion because it might make someone think that the shots were causing abortions. Just a guess though.

“Just one last share. There were occurrences of adverse events in 97.7% of the participants in the ACAM2000 study - do not let anyone you love take that shot. The ACAM2000 product is FDA approved, believe it or not, and does come with some serious warnings.

https://www.drugs.com/pro/acam2000.html

1/3 of all healthy participants experienced an adverse event in the context of the MVA-BN shots. These represent the Modified Vaccinia Ankara (MVA) products made by Bavarian Nordic (BN).

(End of quotes from Dr. Jessica Rose.)

Now, some important highlights from Attorney Tom Renz’s newsletter below:

“With the WHO power grab happening in the background, we also have the monkeypox situation. Monkeypox is a more serious disease than COVID but normally would not spread very easily. Normally is the key word. The problem is that, given how well the gain of function (GoF) work went with COVID, someone apparently thought it would be a good idea to do GoF work on monkeypox (here is a journal document talking about it). This means that we have no idea what we are dealing with now. Is it the original strain of pox? Is it a more contagious strain? We just do not know.

“To further complicate the issue we have the jabs. Monkeypox seem to be inhibited by interferon (read here). The COVID jabs seem to suppress interferon in those that have been jabbed (read here). While certainly not conclusive I am curious whether this means that those that are jabbed will be more susceptible to a disease that would normally not spread very easily. Given that monkeypox normally has a very low reproduction rate (how fast it spreads), my second question would be to ask whether the mass-jabs could be a contributing factor for the borderline panic about a disease that has been around for a while that never presented any sort of large-scale issue (read here about the panic). This question seems even more reasonable when we look at the parallels between the buildup to COVID and what is happening with monkeypox (the Epoch Times does a great job discussing this here and here).”

(End of quote from Attorney Renz.)

My advice:

1. Prayer

2. Alerting everyone to the Plandemic and to NOT PANIC, RESIST TESTING AND LOCKDOWN, AVOID HOSPITALS and VACCINES

3. Ordering Nitazoxanide - seems to be an excellent and safe pox treatment https://www.fredhutch.org/en/news/spotlight/2018/07/hb_hickson_virology.html

The WHO, Monkeypox, and the Continued War on Freedom

Bend over and take your new injection.