I really would liked to have taken part in this discussion. It‘s very interesting. both of you are right. Philip is seeing strange, weird diseases (me too). These MIGHT be infections all over the body (triggered by the virus and/or the immune system). But let‘s be clear: Geert‘s hypothesis is a model. and things in medicine don‘t follow exactly a model. We are all different. So, there will be nor black or white. There will be grey pictures in lots of patients. One more to the colour of black, one more to the colour of white.
While recently picking up paper records at the oncology department from 2022, I saw a healthy man walking into the waiting room. I remember speaking with him in 2022 when he was slumped in a wheelchair with his arms hanging limply.
I asked him about his recovery and treatment. He didn't remember me, indicating that his brain was not functioning properly at the time. However, he answered that four blood transfusions between 2022 and 2023, using blood from a younger, non-vaccinated relative, brought him back on his feet.
Could a blood transfusion from a matching donor who has never had COVID-19 and is non-vaccinated indeed restore the immune system of a very sick person?
When this virus emerges, the end of the world as we know will begin. The health care system will quickly break down. People will be dying at home. Death will be everywhere. Both Dr. Rob and Dr. McMillian know what is coming. They are trying save anyone they can through information about anti-virals. But they know that millions will soon die quick horrible deaths that cannot be treated.
We are at a point where we are facing both COVID and the vaccine situation, which has made me reflect on our immune system, ever since I saw the cartoon "Once Upon a Time... Life - Toxin Wars" in 1988.
The illustration showed how T and B cells, trained by the thymus, memorize intruders and attack invaders in conjunction with the rest of the immune defense in case of infection. Particularly alarming were the cytokines, which seemed unstoppable and destroyed both friend and foe, especially the red blood cells (RBCs).
Ever since then, I have wondered what would happen when a virus or bacterium, unknown to the defense system, enters the body. What would occur if the thymus is compromised, cytochrome P450 is out of commission, adrenaline damages the walls of epithelial cells, and heparin reacts excessively or insufficiently by destroying fibrinogens or creating clots that block veins and arteries, leading to heart problems?
Questions also arise about what happens to all the exhausted macrophages and how overloaded lysosomes release viruses instead of recycling cellular debris. How can organs or brain systems continue to function while inflamed, especially after extensive apoptosis leads to cell death?
Additionally, there is the question of how mitochondria can recover if necessary nutrients, minerals, and vitamins cannot reach this restorative powerhouse.
COVID and the vaccine have presented challenges that necessitate a reevaluation of the endocrine and lymphatic systems, as well as fundamental organ functions, to identify and support the restoration of natural functions without resorting to potentially harmful pharmaceuticals.
I can’t help but think about the end of the interview. The two of you are discussing that for some ppl, avoiding the virus and taking preventative antivirals is the only option. How realistic is that long term? Will the last variant basically go extinct once it burns through the population? Because I’m the highly vaccinated that don’t have immune defenses left, taking ivermectin for the rest of their lives does not seem realistic. When would they be on the clear, if ever?
I’m a new subscriber, while immediate family is unvaccinated, but my siblings and all my nephews have been vaccinated and this is why I ask. Thank you in advance.
Excerpt: Now that we all have a great understanding of the CRISPR/Cas-9 system and how humans are exploiting this system to do gene therapy and stuff, let’s get back to why we’re interested in this subject matter in the first place.
Recently, sequencing of COVID-19 modified mRNA Pfizer vials has revealed the presence of SV40 enhancer. Vials sequenced by Medical Genomics (work reproduced) revealed the enhancer as part of the plasmid map used for production of the modified mRNA - not disclosed by Pfizer or BioNTech in the ‘original plasmid map’ released - as indicated in this version of the Rolling Rapporteur report.12 Currently, both Health Canada (HC) and the European Medicines Agency (EMA) admit to its presence.13 This was just one bit of DNA discovered of the billions of fragments also discovered in both mono and bivalent Pfizer vials, by the way.
The SV40 enhancer is a very useful as a gene therapy tool because it’s a nuclear localization sequence (NLS): it’s very efficient at trafficking stuff to the nuclei of cells. You can read about that here.14 If this is the first time you’re finding out about this, then you’re probably wondering why in the ‘H’ this NLS is in this Pfizer plasmids/vials. It really doesn’t serve a function as per the manufacturing process, so it doesn’t need to be there. It’s a mammalian expression promoter.15 You would be right to wonder.
The concern that a few of us have expressed having discovered (and learned about) this superfluous DNA in the vials, is its potential integration into the genomes of the cells transfected by the modified mRNA LNPs, injected into billions of people as part of the COVID-19 injection roll-out madness (I wish Substack had an option for a creepy font). Random integration events can result in genomic instability and can lead to such things as cancer, especially if they occur in essential genes.
In January this year a friend with chronic lymphocite leukaemia, so no B cells, no antibodies, highly vaccinated died very rapidly with covid - within 10 days. They tried every treatment but nothing worked! They said she had caught a virulent form of the virus. Makes you think!
"Mounting evidence indicates that these vaccines, like many others, do not generate sterilizing immunity, leaving people vulnerable to recurrent infections. Additionally, it has been discovered that the mRNA vaccines inhibit essential immunological pathways, thus impairing early interferon signaling. Within the framework of COVID-19 vaccination, this inhibition ensures an appropriate spike protein synthesis and a reduced immune activation. Evidence is provided that adding 100 % of N1-methyl-pseudouridine (m1Ψ) to the mRNA vaccine in a melanoma model stimulated cancer growth and metastasis, while non-modified mRNA vaccines induced opposite results, thus suggesting that COVID-19 mRNA vaccines could aid cancer development."
Scary scenario and attractive hypothesis. Is there any laboratory data that supports it? The selective encephalopathy suggested by Philip raises a 'zombie' condition- hopefully not flesh eating!
Spike protein could remain in immune cells for more than 245 days following vaccination, according to a recent preprint. The study evaluated 50 patients who developed long COVID-like symptoms after the COVID-19 vaccine; none had been infected with the virus.
The recommendation to take anti-virals such as Ivermectin before getting sick, or exposed to the upcoming HIVICON - won't this just delay the inevitable? A person takes Ivermectin this summer and survives, then this fall or winter or next spring another variant comes along, do they take Ivermectin for the rest of their lives?
I really would liked to have taken part in this discussion. It‘s very interesting. both of you are right. Philip is seeing strange, weird diseases (me too). These MIGHT be infections all over the body (triggered by the virus and/or the immune system). But let‘s be clear: Geert‘s hypothesis is a model. and things in medicine don‘t follow exactly a model. We are all different. So, there will be nor black or white. There will be grey pictures in lots of patients. One more to the colour of black, one more to the colour of white.
Antivirals won‘t work. That‘s exactly why Geert is propagating taking antivirals PROPHYLACTICALLY. Rob states this just right at the end.
A challenging question for clinicians:
While recently picking up paper records at the oncology department from 2022, I saw a healthy man walking into the waiting room. I remember speaking with him in 2022 when he was slumped in a wheelchair with his arms hanging limply.
I asked him about his recovery and treatment. He didn't remember me, indicating that his brain was not functioning properly at the time. However, he answered that four blood transfusions between 2022 and 2023, using blood from a younger, non-vaccinated relative, brought him back on his feet.
Could a blood transfusion from a matching donor who has never had COVID-19 and is non-vaccinated indeed restore the immune system of a very sick person?
Don‘t forget the IgG4!!!!!!! These people WILL get VERY sick. Just now already.
When this virus emerges, the end of the world as we know will begin. The health care system will quickly break down. People will be dying at home. Death will be everywhere. Both Dr. Rob and Dr. McMillian know what is coming. They are trying save anyone they can through information about anti-virals. But they know that millions will soon die quick horrible deaths that cannot be treated.
We are at a point where we are facing both COVID and the vaccine situation, which has made me reflect on our immune system, ever since I saw the cartoon "Once Upon a Time... Life - Toxin Wars" in 1988.
The illustration showed how T and B cells, trained by the thymus, memorize intruders and attack invaders in conjunction with the rest of the immune defense in case of infection. Particularly alarming were the cytokines, which seemed unstoppable and destroyed both friend and foe, especially the red blood cells (RBCs).
Ever since then, I have wondered what would happen when a virus or bacterium, unknown to the defense system, enters the body. What would occur if the thymus is compromised, cytochrome P450 is out of commission, adrenaline damages the walls of epithelial cells, and heparin reacts excessively or insufficiently by destroying fibrinogens or creating clots that block veins and arteries, leading to heart problems?
Questions also arise about what happens to all the exhausted macrophages and how overloaded lysosomes release viruses instead of recycling cellular debris. How can organs or brain systems continue to function while inflamed, especially after extensive apoptosis leads to cell death?
Additionally, there is the question of how mitochondria can recover if necessary nutrients, minerals, and vitamins cannot reach this restorative powerhouse.
COVID and the vaccine have presented challenges that necessitate a reevaluation of the endocrine and lymphatic systems, as well as fundamental organ functions, to identify and support the restoration of natural functions without resorting to potentially harmful pharmaceuticals.
Dr. McMillan,
I can’t help but think about the end of the interview. The two of you are discussing that for some ppl, avoiding the virus and taking preventative antivirals is the only option. How realistic is that long term? Will the last variant basically go extinct once it burns through the population? Because I’m the highly vaccinated that don’t have immune defenses left, taking ivermectin for the rest of their lives does not seem realistic. When would they be on the clear, if ever?
I’m a new subscriber, while immediate family is unvaccinated, but my siblings and all my nephews have been vaccinated and this is why I ask. Thank you in advance.
What antivirals are needed? Is Ivermectin regarded as in this role
Very interesting and very scary.
This is from “Have we been CRISPRed for the coming Cas-9?”
https://jessicar.substack.com/p/have-we-been-crispred-for-the-coming?utm_source=multiple-personal-recommendations-email&utm_medium=email&triedRedirect=true
Excerpt: Now that we all have a great understanding of the CRISPR/Cas-9 system and how humans are exploiting this system to do gene therapy and stuff, let’s get back to why we’re interested in this subject matter in the first place.
Recently, sequencing of COVID-19 modified mRNA Pfizer vials has revealed the presence of SV40 enhancer. Vials sequenced by Medical Genomics (work reproduced) revealed the enhancer as part of the plasmid map used for production of the modified mRNA - not disclosed by Pfizer or BioNTech in the ‘original plasmid map’ released - as indicated in this version of the Rolling Rapporteur report.12 Currently, both Health Canada (HC) and the European Medicines Agency (EMA) admit to its presence.13 This was just one bit of DNA discovered of the billions of fragments also discovered in both mono and bivalent Pfizer vials, by the way.
The SV40 enhancer is a very useful as a gene therapy tool because it’s a nuclear localization sequence (NLS): it’s very efficient at trafficking stuff to the nuclei of cells. You can read about that here.14 If this is the first time you’re finding out about this, then you’re probably wondering why in the ‘H’ this NLS is in this Pfizer plasmids/vials. It really doesn’t serve a function as per the manufacturing process, so it doesn’t need to be there. It’s a mammalian expression promoter.15 You would be right to wonder.
The concern that a few of us have expressed having discovered (and learned about) this superfluous DNA in the vials, is its potential integration into the genomes of the cells transfected by the modified mRNA LNPs, injected into billions of people as part of the COVID-19 injection roll-out madness (I wish Substack had an option for a creepy font). Random integration events can result in genomic instability and can lead to such things as cancer, especially if they occur in essential genes.
In January this year a friend with chronic lymphocite leukaemia, so no B cells, no antibodies, highly vaccinated died very rapidly with covid - within 10 days. They tried every treatment but nothing worked! They said she had caught a virulent form of the virus. Makes you think!
Review: N1-methyl-pseudouridine (m1Ψ): Friend or foe of cancer?
https://pubmed.ncbi.nlm.nih.gov/38583833/
"Mounting evidence indicates that these vaccines, like many others, do not generate sterilizing immunity, leaving people vulnerable to recurrent infections. Additionally, it has been discovered that the mRNA vaccines inhibit essential immunological pathways, thus impairing early interferon signaling. Within the framework of COVID-19 vaccination, this inhibition ensures an appropriate spike protein synthesis and a reduced immune activation. Evidence is provided that adding 100 % of N1-methyl-pseudouridine (m1Ψ) to the mRNA vaccine in a melanoma model stimulated cancer growth and metastasis, while non-modified mRNA vaccines induced opposite results, thus suggesting that COVID-19 mRNA vaccines could aid cancer development."
Scary scenario and attractive hypothesis. Is there any laboratory data that supports it? The selective encephalopathy suggested by Philip raises a 'zombie' condition- hopefully not flesh eating!
"Vaccinated People Show Long COVID-Like Symptoms With Detectable Spike Proteins: Preprint Study": https://www.theepochtimes.com/health/vaccinated-people-show-long-covid-like-symptoms-with-detectable-spike-protein-245-days-after-vaccination-preprint-study-5617223
Spike protein could remain in immune cells for more than 245 days following vaccination, according to a recent preprint. The study evaluated 50 patients who developed long COVID-like symptoms after the COVID-19 vaccine; none had been infected with the virus.
Would this mean 𝘽𝘼.4/5 𝙞𝙣𝙛𝙚𝙘𝙩𝙞𝙤𝙣 renders antibodies, leaving the infected completely defenseless?
Emerging variants develop total escape from potent monoclonal antibodies induced by BA.4/5 infection: https://www.nature.com/articles/s41467-024-47393-3
The recommendation to take anti-virals such as Ivermectin before getting sick, or exposed to the upcoming HIVICON - won't this just delay the inevitable? A person takes Ivermectin this summer and survives, then this fall or winter or next spring another variant comes along, do they take Ivermectin for the rest of their lives?
You talk about taking antivirals but do we buy that in UK?