I told my pharmacist about the CJD cases caused by the vax. He didn't believe me. Now, if I want to, I can show him this.
My MIL has a friend who has recently been diagnosed with CJD. The doctors said that she has a genetic propensity for it, but that doesn't mean that the vax didn't cause it in my opinion.
The way I see it, our bodies are in equilibrium with both cancers and prions.
Both appear all the time and are scrubbed by the body. So I expect everyone has some some prion proteins which could form plaques, but most people keep them under control.
Some people get cancer because their cancer clearing systems work less well than average. I expect, in the same way, some people are prone to prion dementia because their bodies are less good at clearing prions. These people may never normally get dementia in a lifetime unless something happens to shift the equilibrium and generate more prions than their body can clear.
This is what I reckon is happening in those people who get CJD after the vax, they can't clear the prion proteins like we can.
Yes and according to the video I posted last night, this makes perfect sense as your body if flooded w/ more than it can possible handle or deal w/ in a normal manner.
Abstract: Creutzfeldt-Jakob Disease, the formerly rare but universally fatal prion disease in humans, normally progresses over several decades before it leads to death. In the Appendix to this paper, we highlight the presence of a prion region in the spike protein of the original SARS-CoV-2, and in all the “vaccine” variants built from the Wuhan virus. The prion region in the spike of SARS-CoV-2 has a density of mutations eight times greater than that of the rest of the spike, and, yet, strangely that entire prion region disappears completely in the Omicron variant. In the main body of our text, we present 26 cases of Creuzfeldt-Jacob Disease, all diagnosed in 2021 with the first symptoms appearing within an average of 11.38 days after a Pfizer, Moderna, or AstraZeneca COVID-19 injection. Because the causal progression, the etiopathogenesis, of these atypical and new cases of human prion disease — cases of what is apparently a totally new form of rapidly developing Creuzfeldt-Jacob Disease — we focus on the chronology of the symptomatic development. We consider it from an anamnestic point of view — one in which we compare the typical development of pre-COVID cases of Creuzfeldt-Jacob Disease to the extremely accelerated development of similar symptoms in the 26 cases under examination. By such an approach, we hope to work out the etiopathogenesis critical to understanding this new and much more rapidly developing human prion disease. By recalling the sequential pathway of that the formerly subacute and slowly developing disease followed in the past, and by comparing it with this new, extremely acute, rapidly developing prion disease — one following closely after one or more of the COVID-19 injections — we believe it is correct to infer that the injections caused the disease in these 26 cases. If so, they have probably also caused a many other cases that have gone undiagnosed because of their rapid progression to death. By late 2021, 20 had died within 4.76 months of the offending injection. Of those, 8 died suddenly within 2.5 months confirming the rapid progression of this accelerated form of Creuzfeldt-Jacob Disease. By June 2022, 5 more patients had died, and at the time of this current writing, only 1 remains still alive.
Author Biography: Luc Montagnier, Virology; discoverer of the human immunodeficiency virus and Nobel Laureate 2008 Luc Montagnier, MD, and Nobel Laureate, esteemed colleague and friend, passed from this world on February 8, 2022 not long after the completion of the preliminary draft of this work which his co-authors have carried forward to this updated report with some additional cases and new information. Perhaps this may be the most important work of Luc’s lifetime expressing his incredible genius and spirit. While hospitalized, he continued to attach the greatest importance to the publication of this article. He is honored by the Luc Montagnier Foundation Quai Gustave-Ador 62 1207, Geneva, Switzerland.
I told my pharmacist about the CJD cases caused by the vax. He didn't believe me. Now, if I want to, I can show him this.
My MIL has a friend who has recently been diagnosed with CJD. The doctors said that she has a genetic propensity for it, but that doesn't mean that the vax didn't cause it in my opinion.
Thank you fren.
Yes, it may have been dormant and the jab caused it to awaken like we are hearing w/ so many cancers in the vaxxed. Sorry for your friend though.
The way I see it, our bodies are in equilibrium with both cancers and prions.
Both appear all the time and are scrubbed by the body. So I expect everyone has some some prion proteins which could form plaques, but most people keep them under control.
Some people get cancer because their cancer clearing systems work less well than average. I expect, in the same way, some people are prone to prion dementia because their bodies are less good at clearing prions. These people may never normally get dementia in a lifetime unless something happens to shift the equilibrium and generate more prions than their body can clear.
This is what I reckon is happening in those people who get CJD after the vax, they can't clear the prion proteins like we can.
Yes and according to the video I posted last night, this makes perfect sense as your body if flooded w/ more than it can possible handle or deal w/ in a normal manner.
If you show this journal to a doctor, they will laugh at you.
Abstract: Creutzfeldt-Jakob Disease, the formerly rare but universally fatal prion disease in humans, normally progresses over several decades before it leads to death. In the Appendix to this paper, we highlight the presence of a prion region in the spike protein of the original SARS-CoV-2, and in all the “vaccine” variants built from the Wuhan virus. The prion region in the spike of SARS-CoV-2 has a density of mutations eight times greater than that of the rest of the spike, and, yet, strangely that entire prion region disappears completely in the Omicron variant. In the main body of our text, we present 26 cases of Creuzfeldt-Jacob Disease, all diagnosed in 2021 with the first symptoms appearing within an average of 11.38 days after a Pfizer, Moderna, or AstraZeneca COVID-19 injection. Because the causal progression, the etiopathogenesis, of these atypical and new cases of human prion disease — cases of what is apparently a totally new form of rapidly developing Creuzfeldt-Jacob Disease — we focus on the chronology of the symptomatic development. We consider it from an anamnestic point of view — one in which we compare the typical development of pre-COVID cases of Creuzfeldt-Jacob Disease to the extremely accelerated development of similar symptoms in the 26 cases under examination. By such an approach, we hope to work out the etiopathogenesis critical to understanding this new and much more rapidly developing human prion disease. By recalling the sequential pathway of that the formerly subacute and slowly developing disease followed in the past, and by comparing it with this new, extremely acute, rapidly developing prion disease — one following closely after one or more of the COVID-19 injections — we believe it is correct to infer that the injections caused the disease in these 26 cases. If so, they have probably also caused a many other cases that have gone undiagnosed because of their rapid progression to death. By late 2021, 20 had died within 4.76 months of the offending injection. Of those, 8 died suddenly within 2.5 months confirming the rapid progression of this accelerated form of Creuzfeldt-Jacob Disease. By June 2022, 5 more patients had died, and at the time of this current writing, only 1 remains still alive.
Author Biography: Luc Montagnier, Virology; discoverer of the human immunodeficiency virus and Nobel Laureate 2008 Luc Montagnier, MD, and Nobel Laureate, esteemed colleague and friend, passed from this world on February 8, 2022 not long after the completion of the preliminary draft of this work which his co-authors have carried forward to this updated report with some additional cases and new information. Perhaps this may be the most important work of Luc’s lifetime expressing his incredible genius and spirit. While hospitalized, he continued to attach the greatest importance to the publication of this article. He is honored by the Luc Montagnier Foundation Quai Gustave-Ador 62 1207, Geneva, Switzerland.