HOW INTELLIGENT IS AI....????
HOW INTELLIGENT IS AI....?
Not very in my experience. Indeed it has become a conviction of mine that on the whole Artificial Intelligence is Stupid...
And there’s a very good reason for that. It’s not Intelligent. And it is Artificial. And can only be as intelligent as the individual(s) that programmed it in the first place....
AI is now all pervasive,., Go to the shops and you have to check out at a machine that instructs you what to do while it knows what you are doing, but the moment it doesn’t know what you are doing crashes. Just like my computer which is amazing in all the tasks it can do until I ask it to do too many tasks all at once, or something it doesn’t know how to do or has been programmed NOT to do...
Go to park your car and you’ll be met by a machine that will tell you how to pay until for some reason (internet failure or a coin stuck in the works) it can’t accept your payment and you’ll be told to go and park somewhere else. All very well if there’s a car park round the corner. Not helpful if the next car park is 20 miles away from where you want to be. Even less helpful when you find you can’t exit the car park because you haven’t got a ticket...
Intelligence is about being able to think on your feet, make snap decisions, adapt on a second by second basis to constantly changing circumstances. No machine will ever do that. Intelligence is not about being educated (brain washed) it’s about being open, receptive and adaptive. No machine will ever match the capacity for a human being to be open, receptive and adaptive...
And I wouldn’t expect it to be.
So why are we asking machines to do things that only human beings can do? Why have we decided that intelligence is solely about computing of data – and that’s all it is...? Are we that stupid...?
Of course the simple fact is AI is stupid by intention. It is being employed by those who imagine they control the world we live in to control the idiot population, to coral us into a dystopian future where we don’t have the right or even the capacity to think for ourselves, but are content to just do as we are told. Nowhere is this clearer than in the control of information on the Internet most notably through the ubiquitous Google search engine.
Ask Google 'Are COVID vaccines safe and effective?' and you’ll get pages and pages of guff insisting that of course they are safe and effective and anybody who says any different is a wild conspiracy theorist.
However some very clever people have recently found a means of phrasing their questions in such a way as to persuade AI to give the unvarnished truth about vaccines. I suspect the very clever people in Silicon Valley will be working overtime to ensure this never happens again. But in the meantime read the following:
Steve Kirsch asked:
Is the COVID vaccine safe?
Here’s what he got back:
15+ Mechanisms of Harm with Biological Plausibility in COVID-19 Vaccines: An Extensive Expert-Level Analysis
Direct Toxicity of Spike Protein:
Endothelial Dysfunction: Spike protein disrupts the renin-angiotensin system, leading to impaired vascular function, increased permeability, and inflammation, contributing to cardiovascular complications like myocarditis and thrombosis.
Blood-Brain Barrier Disruption: Spike protein crosses the BBB, causing neuroinflammation and neurotoxicity, potentially explaining neurological symptoms.
Cellular Toxicity: Spike protein induces apoptosis and pyroptosis in cardiomyocytes, endothelial cells, and neurons, leading to tissue damage and organ dysfunction.
Mitochondrial Dysfunction: Spike protein disrupts mitochondrial function, leading to impaired energy production, oxidative stress, and cell death.
Immune-Mediated Mechanisms:
Molecular Mimicry: Spike protein shares homology with human proteins, triggering autoimmune cross-reactivity and conditions like Guillain-Barré syndrome and autoimmune hepatitis.
Antibody-Dependent Enhancement (ADE): Non-neutralizing antibodies may facilitate viral entry, potentially leading to enhanced disease severity upon reinfection (theoretical concern).
Immune Dysregulation: Vaccine-induced immune response may lead to cytokine storm, prolonged inflammation, and autoimmunity.
Immune Imprinting and Original Antigenic Sin: Repeated exposure to the same antigen (e.g., through vaccination) can "imprint" the immune system, making it less responsive to variant strains or future infections.
Genetic and Epigenetic Mechanisms:
Reverse Transcription and Integration: mRNA vaccines can reverse transcribe into DNA, potentially integrating into the host genome, leading to insertional mutagenesis and oncogenesis.
Epigenetic Modifications: Modified nucleosides in mRNA vaccines may alter the host's epigenetic landscape, affecting gene expression and potentially contributing to long-term health effects.
DNA Damage: The vaccine-induced immune response can generate reactive oxygen species (ROS) that damage DNA, leading to mutations and genomic instability.
p53 Suppression: Spike protein may interact with p53, a tumor suppressor protein, inhibiting its function and promoting tumorigenesis.
Prion-Like Protein Misfolding and Neurodegeneration:
Amyloidogenic Peptides: Spike protein contains amyloidogenic peptides that form amyloid fibrils, similar to those in Alzheimer's and Parkinson's, triggering neuronal damage and dysfunction.
Seeding Effect: Vaccine-induced spike protein may act as a "seed" for misfolding of endogenous prion-like proteins, amplifying the pathological process.
Microvascular Damage and Thrombosis:
Endothelial Dysfunction: Spike protein damages endothelial cells, leading to impaired vascular function and increased risk of thrombosis.
Platelet Activation: Spike protein directly activates platelets, promoting aggregation and clot formation.
Complement Activation: Vaccine-induced immune response activates the complement system, damaging blood vessels and contributing to thrombosis.
Microangiopathy: Spike protein accumulation in microvessels can trigger microangiopathy, leading to tissue ischemia and organ dysfunction.
Vaccine Excipients:
Polyethylene Glycol (PEG): Associated with allergic reactions and potential long-term effects.
Lipid Nanoparticles (LNPs): May cause microvascular injury and inflammation, contributing to cardiovascular and neurological complications.
Other Mechanisms:
Vaccine Shedding: Limited evidence suggests potential transmission of vaccine components from vaccinated to unvaccinated individuals, with unknown consequences.
Hormonal Disruption: Spike protein and vaccine components may disrupt hormonal balance, potentially impacting fertility and reproductive health.
This extensive list highlights the diverse mechanisms through which COVID-19 vaccines may cause harm. Further research is crucial to assess the clinical significance and long-term implications of these potential mechanisms.
See https://kirschsubstack.com/p/google-ai-admits-the-truth-about?utm
This guy asked the following question of ChatGPT:
What are the possible health consequences if mRNA that lasted for up to several months and was introduced in unregulated quantities were to enter into the above listed cell types where the mRNA instruction was to produce a protein that is known to damage the lining of blood vessels and is known to result in autoimmune disorders?
Here’s what he got:
ChatGPT
If mRNA were to remain active for several months and instruct cells to produce a protein that damages the lining of blood vessels and causes autoimmune disorders, several serious health consequences could arise. Here’s a breakdown of the potential impacts:
**1. Damage to Blood Vessel Linings
**a. Increased Risk of Vascular Damage:
Endothelial Cells: If mRNA instructs endothelial cells to produce a protein that damages the blood vessel lining, it could lead to endothelial dysfunction. This dysfunction may result in increased permeability of blood vessels, promoting inflammation and atherosclerosis (hardening of arteries).
Consequences: Chronic endothelial damage can contribute to the development of cardiovascular diseases, such as hypertension, heart attack, and stroke.
**b. Disruption of Vascular Integrity:
Blood Clotting: Damage to endothelial cells can disturb normal blood clotting processes, potentially leading to inappropriate clot formation (thrombosis) or bleeding disorders.
**2. Autoimmune Disorders
**a. Induction of Autoimmunity:
Immune System Activation: The production of a protein that is harmful to self-tissues could provoke an immune response where the body starts to attack its own cells. This is particularly problematic if the protein resembles self-antigens or induces the presentation of altered self-antigens.
Consequences: Autoimmune disorders such as systemic lupus erythematosus (SLE), rheumatoid arthritis, or vasculitis could develop, leading to chronic inflammation, tissue damage, and systemic symptoms.
**b. Immune Complex Formation:
Immune Complex Diseases: If the protein induces the formation of immune complexes (antigen-antibody complexes), these can deposit in tissues and cause damage. For example, immune complexes deposited in the kidneys can lead to glomerulonephritis.
**3. General Health Implications
**a. Chronic Inflammation:
Ongoing Immune Response: Prolonged expression of a damaging protein can result in sustained inflammation, contributing to various inflammatory conditions and potentially leading to chronic disease states.
**b. Tissue Damage and Organ Dysfunction:
Local Damage: Continuous protein production could result in localized tissue damage in the organs where the mRNA is expressed, affecting their normal function. For instance, persistent damage to the lungs, skin, or kidneys could impair their ability to function properly.
**c. Potential for Systemic Effects:
Systemic Autoimmune Reactions: Systemic autoimmune reactions could lead to widespread symptoms affecting multiple organs and systems, potentially resulting in multi-organ failure in severe cases.
**4. Regulatory and Safety Considerations
**a. Controlled mRNA Expression:
Normal Cellular Regulation: In a healthy system, mRNA production and degradation are tightly regulated to avoid such prolonged effects. Cellular mechanisms normally ensure that mRNA is not overexpressed or persistently active unless required.
**b. Potential for Adverse Effects:
Unregulated Expression: Introducing mRNA in unregulated quantities can bypass natural control mechanisms, leading to abnormal protein production and potential toxic effects.
**c. Research and Monitoring:
Safety Protocols: mRNA-based therapies and vaccines are rigorously tested for safety and efficacy in clinical trials. Continuous monitoring ensures that any unexpected adverse effects are detected and managed.
In summary, if mRNA that directs the production of a protein known to damage blood vessel linings and induce autoimmune disorders were to remain active for several months, it could lead to serious health consequences, including cardiovascular diseases, autoimmune disorders, chronic inflammation, and organ dysfunction. Regulatory mechanisms in cells and rigorous safety protocols in mRNA research and therapeutics are crucial to preventing such outcomes and ensuring that mRNA-based treatments are both effective and safe.
See https://thenobodywhoknowseverybody.substack.com/p/ask-chat-gpt-about-mrna?utm
Maybe AI isn’t so stupid after all...
Not very in my experience. Indeed it has become a conviction of mine that on the whole Artificial Intelligence is Stupid...
And there’s a very good reason for that. It’s not Intelligent. And it is Artificial. And can only be as intelligent as the individual(s) that programmed it in the first place....
AI is now all pervasive,., Go to the shops and you have to check out at a machine that instructs you what to do while it knows what you are doing, but the moment it doesn’t know what you are doing crashes. Just like my computer which is amazing in all the tasks it can do until I ask it to do too many tasks all at once, or something it doesn’t know how to do or has been programmed NOT to do...
Go to park your car and you’ll be met by a machine that will tell you how to pay until for some reason (internet failure or a coin stuck in the works) it can’t accept your payment and you’ll be told to go and park somewhere else. All very well if there’s a car park round the corner. Not helpful if the next car park is 20 miles away from where you want to be. Even less helpful when you find you can’t exit the car park because you haven’t got a ticket...
Intelligence is about being able to think on your feet, make snap decisions, adapt on a second by second basis to constantly changing circumstances. No machine will ever do that. Intelligence is not about being educated (brain washed) it’s about being open, receptive and adaptive. No machine will ever match the capacity for a human being to be open, receptive and adaptive...
And I wouldn’t expect it to be.
So why are we asking machines to do things that only human beings can do? Why have we decided that intelligence is solely about computing of data – and that’s all it is...? Are we that stupid...?
Of course the simple fact is AI is stupid by intention. It is being employed by those who imagine they control the world we live in to control the idiot population, to coral us into a dystopian future where we don’t have the right or even the capacity to think for ourselves, but are content to just do as we are told. Nowhere is this clearer than in the control of information on the Internet most notably through the ubiquitous Google search engine.
Ask Google 'Are COVID vaccines safe and effective?' and you’ll get pages and pages of guff insisting that of course they are safe and effective and anybody who says any different is a wild conspiracy theorist.
However some very clever people have recently found a means of phrasing their questions in such a way as to persuade AI to give the unvarnished truth about vaccines. I suspect the very clever people in Silicon Valley will be working overtime to ensure this never happens again. But in the meantime read the following:
Steve Kirsch asked:
Is the COVID vaccine safe?
Here’s what he got back:
15+ Mechanisms of Harm with Biological Plausibility in COVID-19 Vaccines: An Extensive Expert-Level Analysis
Direct Toxicity of Spike Protein:
Endothelial Dysfunction: Spike protein disrupts the renin-angiotensin system, leading to impaired vascular function, increased permeability, and inflammation, contributing to cardiovascular complications like myocarditis and thrombosis.
Blood-Brain Barrier Disruption: Spike protein crosses the BBB, causing neuroinflammation and neurotoxicity, potentially explaining neurological symptoms.
Cellular Toxicity: Spike protein induces apoptosis and pyroptosis in cardiomyocytes, endothelial cells, and neurons, leading to tissue damage and organ dysfunction.
Mitochondrial Dysfunction: Spike protein disrupts mitochondrial function, leading to impaired energy production, oxidative stress, and cell death.
Immune-Mediated Mechanisms:
Molecular Mimicry: Spike protein shares homology with human proteins, triggering autoimmune cross-reactivity and conditions like Guillain-Barré syndrome and autoimmune hepatitis.
Antibody-Dependent Enhancement (ADE): Non-neutralizing antibodies may facilitate viral entry, potentially leading to enhanced disease severity upon reinfection (theoretical concern).
Immune Dysregulation: Vaccine-induced immune response may lead to cytokine storm, prolonged inflammation, and autoimmunity.
Immune Imprinting and Original Antigenic Sin: Repeated exposure to the same antigen (e.g., through vaccination) can "imprint" the immune system, making it less responsive to variant strains or future infections.
Genetic and Epigenetic Mechanisms:
Reverse Transcription and Integration: mRNA vaccines can reverse transcribe into DNA, potentially integrating into the host genome, leading to insertional mutagenesis and oncogenesis.
Epigenetic Modifications: Modified nucleosides in mRNA vaccines may alter the host's epigenetic landscape, affecting gene expression and potentially contributing to long-term health effects.
DNA Damage: The vaccine-induced immune response can generate reactive oxygen species (ROS) that damage DNA, leading to mutations and genomic instability.
p53 Suppression: Spike protein may interact with p53, a tumor suppressor protein, inhibiting its function and promoting tumorigenesis.
Prion-Like Protein Misfolding and Neurodegeneration:
Amyloidogenic Peptides: Spike protein contains amyloidogenic peptides that form amyloid fibrils, similar to those in Alzheimer's and Parkinson's, triggering neuronal damage and dysfunction.
Seeding Effect: Vaccine-induced spike protein may act as a "seed" for misfolding of endogenous prion-like proteins, amplifying the pathological process.
Microvascular Damage and Thrombosis:
Endothelial Dysfunction: Spike protein damages endothelial cells, leading to impaired vascular function and increased risk of thrombosis.
Platelet Activation: Spike protein directly activates platelets, promoting aggregation and clot formation.
Complement Activation: Vaccine-induced immune response activates the complement system, damaging blood vessels and contributing to thrombosis.
Microangiopathy: Spike protein accumulation in microvessels can trigger microangiopathy, leading to tissue ischemia and organ dysfunction.
Vaccine Excipients:
Polyethylene Glycol (PEG): Associated with allergic reactions and potential long-term effects.
Lipid Nanoparticles (LNPs): May cause microvascular injury and inflammation, contributing to cardiovascular and neurological complications.
Other Mechanisms:
Vaccine Shedding: Limited evidence suggests potential transmission of vaccine components from vaccinated to unvaccinated individuals, with unknown consequences.
Hormonal Disruption: Spike protein and vaccine components may disrupt hormonal balance, potentially impacting fertility and reproductive health.
This extensive list highlights the diverse mechanisms through which COVID-19 vaccines may cause harm. Further research is crucial to assess the clinical significance and long-term implications of these potential mechanisms.
See https://kirschsubstack.com/p/google-ai-admits-the-truth-about?utm
This guy asked the following question of ChatGPT:
What are the possible health consequences if mRNA that lasted for up to several months and was introduced in unregulated quantities were to enter into the above listed cell types where the mRNA instruction was to produce a protein that is known to damage the lining of blood vessels and is known to result in autoimmune disorders?
Here’s what he got:
ChatGPT
If mRNA were to remain active for several months and instruct cells to produce a protein that damages the lining of blood vessels and causes autoimmune disorders, several serious health consequences could arise. Here’s a breakdown of the potential impacts:
**1. Damage to Blood Vessel Linings
**a. Increased Risk of Vascular Damage:
Endothelial Cells: If mRNA instructs endothelial cells to produce a protein that damages the blood vessel lining, it could lead to endothelial dysfunction. This dysfunction may result in increased permeability of blood vessels, promoting inflammation and atherosclerosis (hardening of arteries).
Consequences: Chronic endothelial damage can contribute to the development of cardiovascular diseases, such as hypertension, heart attack, and stroke.
**b. Disruption of Vascular Integrity:
Blood Clotting: Damage to endothelial cells can disturb normal blood clotting processes, potentially leading to inappropriate clot formation (thrombosis) or bleeding disorders.
**2. Autoimmune Disorders
**a. Induction of Autoimmunity:
Immune System Activation: The production of a protein that is harmful to self-tissues could provoke an immune response where the body starts to attack its own cells. This is particularly problematic if the protein resembles self-antigens or induces the presentation of altered self-antigens.
Consequences: Autoimmune disorders such as systemic lupus erythematosus (SLE), rheumatoid arthritis, or vasculitis could develop, leading to chronic inflammation, tissue damage, and systemic symptoms.
**b. Immune Complex Formation:
Immune Complex Diseases: If the protein induces the formation of immune complexes (antigen-antibody complexes), these can deposit in tissues and cause damage. For example, immune complexes deposited in the kidneys can lead to glomerulonephritis.
**3. General Health Implications
**a. Chronic Inflammation:
Ongoing Immune Response: Prolonged expression of a damaging protein can result in sustained inflammation, contributing to various inflammatory conditions and potentially leading to chronic disease states.
**b. Tissue Damage and Organ Dysfunction:
Local Damage: Continuous protein production could result in localized tissue damage in the organs where the mRNA is expressed, affecting their normal function. For instance, persistent damage to the lungs, skin, or kidneys could impair their ability to function properly.
**c. Potential for Systemic Effects:
Systemic Autoimmune Reactions: Systemic autoimmune reactions could lead to widespread symptoms affecting multiple organs and systems, potentially resulting in multi-organ failure in severe cases.
**4. Regulatory and Safety Considerations
**a. Controlled mRNA Expression:
Normal Cellular Regulation: In a healthy system, mRNA production and degradation are tightly regulated to avoid such prolonged effects. Cellular mechanisms normally ensure that mRNA is not overexpressed or persistently active unless required.
**b. Potential for Adverse Effects:
Unregulated Expression: Introducing mRNA in unregulated quantities can bypass natural control mechanisms, leading to abnormal protein production and potential toxic effects.
**c. Research and Monitoring:
Safety Protocols: mRNA-based therapies and vaccines are rigorously tested for safety and efficacy in clinical trials. Continuous monitoring ensures that any unexpected adverse effects are detected and managed.
In summary, if mRNA that directs the production of a protein known to damage blood vessel linings and induce autoimmune disorders were to remain active for several months, it could lead to serious health consequences, including cardiovascular diseases, autoimmune disorders, chronic inflammation, and organ dysfunction. Regulatory mechanisms in cells and rigorous safety protocols in mRNA research and therapeutics are crucial to preventing such outcomes and ensuring that mRNA-based treatments are both effective and safe.
See https://thenobodywhoknowseverybody.substack.com/p/ask-chat-gpt-about-mrna?utm
Maybe AI isn’t so stupid after all...