Professor - Africa lower mortality = biodiversity + antimalarials + antihelminths. Stop hemoglobin interference, stop malaria & C19 or anything requiring iron for proliferation.
Sadly, all this was known prior to 2008. Why do you think Malaria samples were found in that little "black lab"? Airborne AIDS? Happy Weekend, some dream of GMO mosquitos Mr. Mulder.
I have a feeling you are more informed and knowledgable than many, so I will be open =P.
Airborne aids is just a memetic way to describe it, because the correct way would be "PAID" that I named it Paradoxically Acquired Immune >>>Dysfunction<<<. Covid is not causing deficiency, but it is causing dysfunction and killing different types of T-Cells, which I CAN'T make sense of it.
Each variant, and even subvariant suddenly shifts towards different types of immune cells it will kill. To understand where I am coming from just Google Tim-3 Galectin-9 (the predominant Omicron immune response, the opposite of non-Omicron variants, yet...".
I did indeed thought about how there is some iron deprivation in regards to Malaria and how it would protect a Covid infection, but I decided to abstain here from the Ferroptosis aspect of it (I am still heavily invested on that lol).
Oh you are correct, Malaria was there wasn't it. I wonder if one of these labs had JC Virus...hummmmm.
Professor - "Each variant, and even subvariant suddenly shifts towards different types of immune cells it will kill but... it is causing dysfunction and killing different types of T-Cells, which I CAN'T make sense of it."
Sometimes the questions are complicated and the answers are simple. This dysfunction leads to both suppression & deficiency, which can reactivate JC and OTHER latent asymptomatic things. What is the induction of abnormal cell growth?
And sometimes the answer is in the question.
Needs iron for proliferation = malaria, C19 & ? Tim-3 Galectin-9 is a pathway for ? This "family" has an oncogenic mechanism?
"I have a feeling" Memetic or mimetic indeed. One can only go as far as one wants to go. But remember Mr. Mulder... https://youtu.be/w0MN-0i4yW4?t=60
Sorry taking long to reply. Stormed so bad here yesterday that part of my roof flew away (LOL), plus outage of all services".
Since I know if we don't spoonfeed the roaches they won't get it, yes I agree with all your observations and indeed they all share the same mechanisms. I am trying to find why a virus that now has the opposite "immune reaction" still does the same as the first, nasty one. Perhaps one of my early assertions in regards to Omicron was in the right track.
Airborne AIDS for sure. Lots of cancers coming out, mostly brain, lung, hematological, multiple myeloma, and reproductive including breast. Hubby has been coughing for months now and I expect blood any day. Noteworthy that Pfizer purchased cancer giant Seagen back in December 23 which is devoted to all 3. Curiously the solution is always monoclonal antibodies- MABS. I read a paper from U of Penn med school during the covid show explaining how mabs were the perfect delivery system for the mRNA gene therapy. All of sudden Jersey is making Regeneron super available. No surprise. Great work as always- I save them all!!
I wrote a few times on the cancer aspect, I even forecast most of the common cancer in the first and second wave (of cancer). The mRNA and the virus both help with that, but to me it is much more complicated, there are confounding factors that are helping drive these waves of cancer.
And I don't know which is worse, getting cancer early on and avoiding dementia, or getting dementia within years, and avoiding cancer. Both diseases are disgusting.
Oh, for a time I tracked many of Pfizer's and Moderna's acquisitions and deduced based on the patterns they were using machine learning to "guesstimate" which cancers would experience the most growth within 5-10 years and made their bets.
DARPA has a Twitter post literally saying mRNA is a antibody treatment perfect to treat cancer and they partnered with Moderna at the time hehe. MABS and CAR-T cell are all the rage indeed.
The funny part ? The ironic one. MABS most common side-effects, bacterial and fungal infections. CAR-T Cell ? Reactivation of latent Herpes viruses.
Sounds like a good business model with you are a complete psychopath to me lol.
Engineered T-Cell made in labs to treat VERY specific diseases, since you can "engineer" them, you can target very precise what you want.
They are very promising to treat many, many diseases but some of the drawbacks are worrying long-term. Herpes viruses reactivation contribute long-term to a bunch of diseases, so while you treat that nasty condition right now, what the damage will be 10-20 years down the road ? Although I expect they will "fix" this issue within a few years.
I was the person who memed "Covid is airborne AIDS" years ago. Based on observation and scientific curiosity.
Still hope I was wrong. I distanced myself from that because of the abhorly massive number of grifters on that. Very few honest people talk about it honestly (Just doorlesscapr really, very intellectually honest and really smart person).
It does appear that is how it's turning out... altho we do have things to throw at AIDS after all this time....this seems to be worse what with the blood clotting and cardiac issues. Different pathways, I guess.
Ah yes - through various links I found doorlesscrap and then you... good bedtime reading -- thanks!
It also failed in the youngest cohorts it was meant to protect:
Acceptance, availability, and feasibility of RTS, S/AS01 malaria vaccine: A review (2023)
“…Vaccine effectiveness was shown to be significantly lower in clinical trials including infants aged 6–14 weeks compared to children aged 5–17 months. The low efficacy of the RTS, S/AS01 vaccination in babies was supposedly attributable to their underdeveloped immune systems and the interference of maternal antibodies.”
Kinda reminds me of that 2021 paper that linked molecular similarities between RBD and deadly pathogens which stated prior infections or vaccinations with malaria/TB seemed to provide protection against C19 infections 🤔
Tb one is complex but has been "disproved" in some ways. It will end up with a chronic infection and one pathogen can help the other drive severe disease. SARS-CoV-2 will also reactivate lantet TB, there are a few recent (6 months-ish) papers on TB.
Malaria we now have experimental data on how and why, and it is 100% unrelated with the antibodies (therefore the mimicry doesn't play a role, directly), in this particular case. I still think it does play a role, which role ? Who knows, we don't have a lab and those who do, don't test for it lol.
It is pretty interesting that SC2 viral load goes unchecked when exposed to malaria which would indicate immune tolerance/exhaustion. Just proves that innate inflammation remains vitally important
Exhaustion is almost completely different from tolerance though, I also find myself disagreeing with the concept of exhaustion per most papers propose (if it has these or that receptor, it is a exhausted T cell...like the T cell is useless, verifiably untrue).
Per the papers linked at the end, it is most likely some level of tolerance, it would be great to know if it is because TLRs become tolerant for a few weeks, or it is because of the toxin tolerance itself shifting the inflammatory signals.
Ironically enough (I decided to keep this one out for simplicity sake), parasite infections shift your immune system HEAVILY towards Th2. Sounds familiar ?
I just wonder how this relates to someone (like me) that's been suffering with another biotoxin(s) that was unleashed on an unsuspecting populace. I'm talking about lyme, bartonella and babesia which seems closely related to malaria.
There are groups of fellow sufferers with similar infections. I'm definitely not the only one. Any feedback, comments or suggestions?
Dealing with Lyme itself, often using antibiotics, and making use of Activated Charcoal so the body doesnt absorb both the toxins, and the antibiotics byproduces. Same for Bartonella and Babesia, you need to deal with the infection in a active way, since SARS-CoV-2 will often help these wreck havoc on it.
You need to achieve immuno competence so the body can deal with the disease and get rid of it, easier said than done and this process, under normal immunological conditions and health can take months, so it is a complex battle. From my perspective (not super well-versed on these), antibiotics and charcoal are one way to put them into their place and deal with other symptoms and start recovering.
I know its likely impossible to know the real answer to this but, did the creators of the virus had all this interactions in mind? Or perhaps they are a little frustated África had so "little" impact?
Professor - Africa lower mortality = biodiversity + antimalarials + antihelminths. Stop hemoglobin interference, stop malaria & C19 or anything requiring iron for proliferation.
Sadly, all this was known prior to 2008. Why do you think Malaria samples were found in that little "black lab"? Airborne AIDS? Happy Weekend, some dream of GMO mosquitos Mr. Mulder.
https://youtu.be/hoClEqyVJ5U?t=28
I have a feeling you are more informed and knowledgable than many, so I will be open =P.
Airborne aids is just a memetic way to describe it, because the correct way would be "PAID" that I named it Paradoxically Acquired Immune >>>Dysfunction<<<. Covid is not causing deficiency, but it is causing dysfunction and killing different types of T-Cells, which I CAN'T make sense of it.
Each variant, and even subvariant suddenly shifts towards different types of immune cells it will kill. To understand where I am coming from just Google Tim-3 Galectin-9 (the predominant Omicron immune response, the opposite of non-Omicron variants, yet...".
I did indeed thought about how there is some iron deprivation in regards to Malaria and how it would protect a Covid infection, but I decided to abstain here from the Ferroptosis aspect of it (I am still heavily invested on that lol).
Oh you are correct, Malaria was there wasn't it. I wonder if one of these labs had JC Virus...hummmmm.
Professor - "Each variant, and even subvariant suddenly shifts towards different types of immune cells it will kill but... it is causing dysfunction and killing different types of T-Cells, which I CAN'T make sense of it."
Sometimes the questions are complicated and the answers are simple. This dysfunction leads to both suppression & deficiency, which can reactivate JC and OTHER latent asymptomatic things. What is the induction of abnormal cell growth?
And sometimes the answer is in the question.
Needs iron for proliferation = malaria, C19 & ? Tim-3 Galectin-9 is a pathway for ? This "family" has an oncogenic mechanism?
"I have a feeling" Memetic or mimetic indeed. One can only go as far as one wants to go. But remember Mr. Mulder... https://youtu.be/w0MN-0i4yW4?t=60
Sorry taking long to reply. Stormed so bad here yesterday that part of my roof flew away (LOL), plus outage of all services".
Since I know if we don't spoonfeed the roaches they won't get it, yes I agree with all your observations and indeed they all share the same mechanisms. I am trying to find why a virus that now has the opposite "immune reaction" still does the same as the first, nasty one. Perhaps one of my early assertions in regards to Omicron was in the right track.
Twists and turn every single time.
Professor - "part of my roof flew away" at least this didn't happen... https://youtu.be/RQWSh7Db-_E?t=156
"Twists and turn every single time.... why a virus that now has the opposite "immune reaction" still does the same as the first..."
This is why Mr. Mulder... https://youtu.be/oijEsqT2QKQ?
Airborne AIDS for sure. Lots of cancers coming out, mostly brain, lung, hematological, multiple myeloma, and reproductive including breast. Hubby has been coughing for months now and I expect blood any day. Noteworthy that Pfizer purchased cancer giant Seagen back in December 23 which is devoted to all 3. Curiously the solution is always monoclonal antibodies- MABS. I read a paper from U of Penn med school during the covid show explaining how mabs were the perfect delivery system for the mRNA gene therapy. All of sudden Jersey is making Regeneron super available. No surprise. Great work as always- I save them all!!
I wrote a few times on the cancer aspect, I even forecast most of the common cancer in the first and second wave (of cancer). The mRNA and the virus both help with that, but to me it is much more complicated, there are confounding factors that are helping drive these waves of cancer.
And I don't know which is worse, getting cancer early on and avoiding dementia, or getting dementia within years, and avoiding cancer. Both diseases are disgusting.
Oh, for a time I tracked many of Pfizer's and Moderna's acquisitions and deduced based on the patterns they were using machine learning to "guesstimate" which cancers would experience the most growth within 5-10 years and made their bets.
DARPA has a Twitter post literally saying mRNA is a antibody treatment perfect to treat cancer and they partnered with Moderna at the time hehe. MABS and CAR-T cell are all the rage indeed.
The funny part ? The ironic one. MABS most common side-effects, bacterial and fungal infections. CAR-T Cell ? Reactivation of latent Herpes viruses.
Sounds like a good business model with you are a complete psychopath to me lol.
What’s CAR-T cell?
Engineered T-Cell made in labs to treat VERY specific diseases, since you can "engineer" them, you can target very precise what you want.
They are very promising to treat many, many diseases but some of the drawbacks are worrying long-term. Herpes viruses reactivation contribute long-term to a bunch of diseases, so while you treat that nasty condition right now, what the damage will be 10-20 years down the road ? Although I expect they will "fix" this issue within a few years.
Interesting. And what is this "conspiracy theory" you hope never comes true? I need something to worry about... lol
I was the person who memed "Covid is airborne AIDS" years ago. Based on observation and scientific curiosity.
Still hope I was wrong. I distanced myself from that because of the abhorly massive number of grifters on that. Very few honest people talk about it honestly (Just doorlesscapr really, very intellectually honest and really smart person).
It does appear that is how it's turning out... altho we do have things to throw at AIDS after all this time....this seems to be worse what with the blood clotting and cardiac issues. Different pathways, I guess.
Ah yes - through various links I found doorlesscrap and then you... good bedtime reading -- thanks!
If I am being honest, it is far worse than AIDS, yet it leaves severely less "traces" of it.
I may or may not delete this comment I made. And yes different pathways and much more complex.
Moriarty, I'm co-writing a few papers relating to igG4, you are correct and I'm happy to share these:
IgG Subclass Switch in Volunteers Repeatedly Immunized with the Full-Length Plasmodium falciparum Merozoite Surface Protein 1 (MSP1) (2024)
https://www.mdpi.com/2076-393X/12/2/208
Immune escape by the parasite may explain paradoxical outcomes:
Delayed fractional dose regimen of the RTS,S/AS01 malaria vaccine candidate enhances an IgG4 response that inhibits serum opsonophagocytosis (2017)
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5554171/
Lots of deaths and diseases that are all unrelated, of course:
Full Evidence Report on the RTS,S/AS01 Malaria Vaccine (2021)
https://cdn.who.int/media/docs/default-source/immunization/mvip/full-evidence-report-on-the-rtss-as01-malaria-vaccine-for-sage-mpag-(sept2021).pdf
It also failed in the youngest cohorts it was meant to protect:
Acceptance, availability, and feasibility of RTS, S/AS01 malaria vaccine: A review (2023)
“…Vaccine effectiveness was shown to be significantly lower in clinical trials including infants aged 6–14 weeks compared to children aged 5–17 months. The low efficacy of the RTS, S/AS01 vaccination in babies was supposedly attributable to their underdeveloped immune systems and the interference of maternal antibodies.”
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10266133/
Kinda reminds me of that 2021 paper that linked molecular similarities between RBD and deadly pathogens which stated prior infections or vaccinations with malaria/TB seemed to provide protection against C19 infections 🤔
Tb one is complex but has been "disproved" in some ways. It will end up with a chronic infection and one pathogen can help the other drive severe disease. SARS-CoV-2 will also reactivate lantet TB, there are a few recent (6 months-ish) papers on TB.
Malaria we now have experimental data on how and why, and it is 100% unrelated with the antibodies (therefore the mimicry doesn't play a role, directly), in this particular case. I still think it does play a role, which role ? Who knows, we don't have a lab and those who do, don't test for it lol.
It is pretty interesting that SC2 viral load goes unchecked when exposed to malaria which would indicate immune tolerance/exhaustion. Just proves that innate inflammation remains vitally important
Exhaustion is almost completely different from tolerance though, I also find myself disagreeing with the concept of exhaustion per most papers propose (if it has these or that receptor, it is a exhausted T cell...like the T cell is useless, verifiably untrue).
Per the papers linked at the end, it is most likely some level of tolerance, it would be great to know if it is because TLRs become tolerant for a few weeks, or it is because of the toxin tolerance itself shifting the inflammatory signals.
Ironically enough (I decided to keep this one out for simplicity sake), parasite infections shift your immune system HEAVILY towards Th2. Sounds familiar ?
Yessir!
I just wonder how this relates to someone (like me) that's been suffering with another biotoxin(s) that was unleashed on an unsuspecting populace. I'm talking about lyme, bartonella and babesia which seems closely related to malaria.
There are groups of fellow sufferers with similar infections. I'm definitely not the only one. Any feedback, comments or suggestions?
Dealing with Lyme itself, often using antibiotics, and making use of Activated Charcoal so the body doesnt absorb both the toxins, and the antibiotics byproduces. Same for Bartonella and Babesia, you need to deal with the infection in a active way, since SARS-CoV-2 will often help these wreck havoc on it.
You need to achieve immuno competence so the body can deal with the disease and get rid of it, easier said than done and this process, under normal immunological conditions and health can take months, so it is a complex battle. From my perspective (not super well-versed on these), antibiotics and charcoal are one way to put them into their place and deal with other symptoms and start recovering.
I know its likely impossible to know the real answer to this but, did the creators of the virus had all this interactions in mind? Or perhaps they are a little frustated África had so "little" impact?
"Unforseen consequences" as one of my favorite papers put it (Spike Protein as a Endotoxin Delivery System is the title of the paper).
Seeing bird flu being hyped up again. Wonder how that particular virus will affect things when thrown into the mix.