Thanks for sharing. The silence coming from the majority of our fellow medical colleagues is something close to criminal. Corruption and other bad things have taken full control. We must keep talking.
Thanks a lot for this Philip. I am surprised this post was removed, as your wording is very cautious. You do not even mention the vaccines. But then, the censorship seems to be getting worse and worse. My own profile is still restricted. The reasons? Sharing an interesting article on China's foreign policy which appeared in an Indian journal. Sharing an article on the mokeypox simulation last year and how prescient they were. Sharing a peer reviewed study that shows masks don't work. Their problem is they don't seem to have a clue about their own policies. As an example they have not been able to explain to me what a user should do if guidance by health authorities is contradictory, for example regarding child-vaccination, masks or other things, allowed or recommended in some countries but not in others. Reminds you a bit of how the code of law functions in a totalitarian state; the written code is simply irrelevant.
My LinkedIn in account was locked over my comments pointing out the massive failure the mRNA vaccines have been for preventing infection. I’m not going to beg forgiveness for an honest opinion based upon documented case rates, trends etc. I am simply pulling my premium membership. Short LinkedIn.
The highly jabbed/boosted need to realize they are sitting on high titers of *now* non-neutralizing Abs. And recent literature suggests a bias towards IgG4 upon viral challenge - precisely what Abeles implied last summer regarding IVIG-like tolerance to spike and/or antibodies to antigen (e.g., IgG3-N).
One function of neonatal Fc receptors on IgG appears to be transcytosis of Abs and, subsequently, immune complexes formed in gut mucosa comprised of these Abs to systemic vasculature for antigen presentation.
The apparent absence of conclusive aetiology in multisystem pathologies that I've seen recently presented anecdotally seems to indicate that these non-neutralized immune complexes are possibly affecting multiple organs concurrently in the highly jabbed. In contrast, the *never* vaccinated seem to handle continued exposure to these variants as upper respiratory infections via NK cell activation and presumably SIgA produced from tissue resident B cells. Our non immune imprinted GCs are not continually pumping out systemic Abs to Wuhan spike that could potentially outcompete or obviate mucosal derived Abs. Additional reports of lymphopenia, specifically CD8+ exhaustion, upon challenge among the highly vaccinated indicates an absence of robust mucosal immunity.
My own immunothrombotic response to delta nearly killed me last September. When rechallenged with omicron this past June, presumably BA5, there was no complement driven hypercytokinemia, no persistent pulmonary hypertension, no hypercoagulable state, no perceptible long duration rise in IL-6, IL-1ß or TNF-alpha (3-day low grade fever w/om vs 14 days with delta). Initial presentation was 130+ PR and decreased sats - low 90s to upper 80s - that awoke me at 3AM from a dead sleep. Remainder of day 1 was comprised of lower GI irritability. Following days' Sx were entirely upper respiratory in nature. Recovered fully on day 6 and infected no one else in my household despite this variant apparently having an intrinsic R0 greater than measles.
Aug 6, 2022·edited Aug 6, 2022Liked by Dr Philip McMillan
Who are the 100million Dr McMillan? The unvaxxed, the vaxxed, the multi boosted? And does already having or not having covid play a roll in all of it? Please aswer as best you can in laymen terms. I am well aware of yours and Gerts and all our other "Hippocratic Oath Hero's," including both of you's thoughts on all this. In a nut shell, who may be going to pass away and why Dr McMillan? Is it OAS immune imprinting, ADE, pushing a more virulent variant, or staight up autoimmunity reaction for everyone despite infection status or vax status ?
As an admirer of the author's usually detached, rational analysis of medical issues, I am baffled by this sudden descent into near-hysteria.
A deaths sunami on the horizon? Where, pray, is the actual evidence to support the 100 million fatalities forecast? Does it include deaths caused by pseudo-vaccines roll-out, lockdowns, and all the other insane interventions with obvious detrimental public health consequences?
At least, dear doctor, spell out some of the symptoms on which you dire diagnosis was made. Otherwise, I'm staying on the beach to soak up more COVID-defying Vitamin D!
100 million global excess all cause mortality wouldn't shock me at all. imho from all the research I've read throughout the last years this would mark the lower threshold.
it could easily mount up to 10x that number within the next 5 to 10 years given the accelerated cellular aging that occurs when exposed to the spike protein unmitigated. people will age and die much faster than previously. children birthed by vaccinated mothers will have a very hard time establishing a healthy immune system if they make it at all. ... and so on. the list of immune dysfunctions will be growing every day. ... treatments will be available but hard to roll out with success on a massive scale to a population that is ridden with co-morbidities already.
the people who are in good mental and physical health will likely make it somehow. but whoever is poisoned with glyphosate, obese and with other co-morbidities I'm seriously concerned for.
Become healthy everybody, as long as you still can.
When you open the Overton window over the topics that expose aggregate consequences from a long-term perspective, be it monetary policy or health policy, you inevitably share shocking material. And sharing shocking material is prohibited on LI. So, you should either conceal the aggregates or restrict the depth of your perspective to fit in the LI’s Overton window. However, LI censorship module is sensitive when you use metaphors like tsunami, storm, cataclysm or other phenomenon dependent on a butterfly effect.
Thanks Dr McMillan much appreciated i suspect this is going to happen
S2-targeting non-NAbs could participate in the physiopathology of COVID-19. Indeed, it has been shown that chronic (over)activation of the immune system can lead to the development of autoimmune disease through the expansion of auto- and/or polyreactive clone's
Emerging data indicate that the Omicron variant evades neutralization by sera obtained from people vaccinated with 1 or 2 doses of vaccine, especially when antibody titres are waning. Indicative studies have shown that 3 doses of spike-based vaccines may provide only partial protection from infection with this variant. Immune evasion by Omicron may have contributed to the extremely high transmission rates in countries with high vaccination rates or natural immunity (R0 of 3–5
Timing is everything. Many organisms across the tree of life have evolved timekeeping mechanisms that regulate numerous of their cellular functions to optimize timing by anticipating changes in the environment. The specific environmental changes that are sensed depends on the organism. For animals, plants, and free-living microbes, environmental cues include light/dark cycles, daily temperature fluctuations, among others. In contrast, for a microbe that is never free-living,
Timing is everything. Many organisms across the tree of life have evolved timekeeping mechanisms that regulate numerous of their cellular functions to optimize timing by anticipating changes in the environment. The specific environmental changes that are sensed depends on the organism. For animals, plants, and free-living microbes, environmental cues include light/dark cycles, daily temperature fluctuations, among others. In contrast, for a microbe that is never free-living
Thanks for sharing. The silence coming from the majority of our fellow medical colleagues is something close to criminal. Corruption and other bad things have taken full control. We must keep talking.
Thanks a lot for this Philip. I am surprised this post was removed, as your wording is very cautious. You do not even mention the vaccines. But then, the censorship seems to be getting worse and worse. My own profile is still restricted. The reasons? Sharing an interesting article on China's foreign policy which appeared in an Indian journal. Sharing an article on the mokeypox simulation last year and how prescient they were. Sharing a peer reviewed study that shows masks don't work. Their problem is they don't seem to have a clue about their own policies. As an example they have not been able to explain to me what a user should do if guidance by health authorities is contradictory, for example regarding child-vaccination, masks or other things, allowed or recommended in some countries but not in others. Reminds you a bit of how the code of law functions in a totalitarian state; the written code is simply irrelevant.
My LinkedIn in account was locked over my comments pointing out the massive failure the mRNA vaccines have been for preventing infection. I’m not going to beg forgiveness for an honest opinion based upon documented case rates, trends etc. I am simply pulling my premium membership. Short LinkedIn.
The highly jabbed/boosted need to realize they are sitting on high titers of *now* non-neutralizing Abs. And recent literature suggests a bias towards IgG4 upon viral challenge - precisely what Abeles implied last summer regarding IVIG-like tolerance to spike and/or antibodies to antigen (e.g., IgG3-N).
One function of neonatal Fc receptors on IgG appears to be transcytosis of Abs and, subsequently, immune complexes formed in gut mucosa comprised of these Abs to systemic vasculature for antigen presentation.
The apparent absence of conclusive aetiology in multisystem pathologies that I've seen recently presented anecdotally seems to indicate that these non-neutralized immune complexes are possibly affecting multiple organs concurrently in the highly jabbed. In contrast, the *never* vaccinated seem to handle continued exposure to these variants as upper respiratory infections via NK cell activation and presumably SIgA produced from tissue resident B cells. Our non immune imprinted GCs are not continually pumping out systemic Abs to Wuhan spike that could potentially outcompete or obviate mucosal derived Abs. Additional reports of lymphopenia, specifically CD8+ exhaustion, upon challenge among the highly vaccinated indicates an absence of robust mucosal immunity.
My own immunothrombotic response to delta nearly killed me last September. When rechallenged with omicron this past June, presumably BA5, there was no complement driven hypercytokinemia, no persistent pulmonary hypertension, no hypercoagulable state, no perceptible long duration rise in IL-6, IL-1ß or TNF-alpha (3-day low grade fever w/om vs 14 days with delta). Initial presentation was 130+ PR and decreased sats - low 90s to upper 80s - that awoke me at 3AM from a dead sleep. Remainder of day 1 was comprised of lower GI irritability. Following days' Sx were entirely upper respiratory in nature. Recovered fully on day 6 and infected no one else in my household despite this variant apparently having an intrinsic R0 greater than measles.
Who are the 100million Dr McMillan? The unvaxxed, the vaxxed, the multi boosted? And does already having or not having covid play a roll in all of it? Please aswer as best you can in laymen terms. I am well aware of yours and Gerts and all our other "Hippocratic Oath Hero's," including both of you's thoughts on all this. In a nut shell, who may be going to pass away and why Dr McMillan? Is it OAS immune imprinting, ADE, pushing a more virulent variant, or staight up autoimmunity reaction for everyone despite infection status or vax status ?
Dr Phillip as always many thanks.
Continually pointing out, not just, The Elephant in the Room.
But the whole herd of elephants in the room!
Keep on Keeping on please. Thank you so much.
As an admirer of the author's usually detached, rational analysis of medical issues, I am baffled by this sudden descent into near-hysteria.
A deaths sunami on the horizon? Where, pray, is the actual evidence to support the 100 million fatalities forecast? Does it include deaths caused by pseudo-vaccines roll-out, lockdowns, and all the other insane interventions with obvious detrimental public health consequences?
At least, dear doctor, spell out some of the symptoms on which you dire diagnosis was made. Otherwise, I'm staying on the beach to soak up more COVID-defying Vitamin D!
I thank you so much for your excellent work Dr Philip McMillan.
It’s our health and our future that depends upon on the strength and maturity of our innate immune systems!
100 million global excess all cause mortality wouldn't shock me at all. imho from all the research I've read throughout the last years this would mark the lower threshold.
it could easily mount up to 10x that number within the next 5 to 10 years given the accelerated cellular aging that occurs when exposed to the spike protein unmitigated. people will age and die much faster than previously. children birthed by vaccinated mothers will have a very hard time establishing a healthy immune system if they make it at all. ... and so on. the list of immune dysfunctions will be growing every day. ... treatments will be available but hard to roll out with success on a massive scale to a population that is ridden with co-morbidities already.
the people who are in good mental and physical health will likely make it somehow. but whoever is poisoned with glyphosate, obese and with other co-morbidities I'm seriously concerned for.
Become healthy everybody, as long as you still can.
When you open the Overton window over the topics that expose aggregate consequences from a long-term perspective, be it monetary policy or health policy, you inevitably share shocking material. And sharing shocking material is prohibited on LI. So, you should either conceal the aggregates or restrict the depth of your perspective to fit in the LI’s Overton window. However, LI censorship module is sensitive when you use metaphors like tsunami, storm, cataclysm or other phenomenon dependent on a butterfly effect.
Thanks Dr McMillan much appreciated i suspect this is going to happen
S2-targeting non-NAbs could participate in the physiopathology of COVID-19. Indeed, it has been shown that chronic (over)activation of the immune system can lead to the development of autoimmune disease through the expansion of auto- and/or polyreactive clone's
https://www.sciencedirect.com/science/article/abs/pii/S1084952121002391
Circadian rhythms in infectious diseases and symbiosis
The clocks that time us
Emerging data indicate that the Omicron variant evades neutralization by sera obtained from people vaccinated with 1 or 2 doses of vaccine, especially when antibody titres are waning. Indicative studies have shown that 3 doses of spike-based vaccines may provide only partial protection from infection with this variant. Immune evasion by Omicron may have contributed to the extremely high transmission rates in countries with high vaccination rates or natural immunity (R0 of 3–5
Cross-reactive immunity against SARS-CoV-2 N protein in Central and West Africa precedes the COVID-19 pandemic
Jannie Pedersen, Ismaël Hervé Koumakpayi
Timing is everything. Many organisms across the tree of life have evolved timekeeping mechanisms that regulate numerous of their cellular functions to optimize timing by anticipating changes in the environment. The specific environmental changes that are sensed depends on the organism. For animals, plants, and free-living microbes, environmental cues include light/dark cycles, daily temperature fluctuations, among others. In contrast, for a microbe that is never free-living,
Timing is everything. Many organisms across the tree of life have evolved timekeeping mechanisms that regulate numerous of their cellular functions to optimize timing by anticipating changes in the environment. The specific environmental changes that are sensed depends on the organism. For animals, plants, and free-living microbes, environmental cues include light/dark cycles, daily temperature fluctuations, among others. In contrast, for a microbe that is never free-living