I know of a late 40's vxxxd female in excellent health with a "cut" that reportedly became infected, she developed sepsis. Lost one leg and I heard both hands were in danger of being amputated. No one mentioned mRNA injections and their adverse affects on the immune system.
Dr. Geert Vanden Bossche is still trying to defend his tribe of vaccinologists by being luke-warm on Bobby and by accepting "not-perfect" MMR & Dtap vaccines. At least he rejects all other vaccines, including polio and Covid.
He is right when he says CLEAN WATER is more important and the vaccine-derived polio is worse than wild polio.
Wow, thousands and thousands of people should be hearing this and reading the comments, and I cannot believe that only 98 have liked it, and 23 responded? If that isn't proof of suppression and censorship, then I don't know what else to tell you...carry on, faithful soldier!
(2 of 2) Chauss et al. studied Th1 cells from the lungs of hospitalised COVID-19 patients.
They found that the cells' intracine signaling system was being activated as it should be, with the 1-hydroxlase enzyme and VDR being produced in the cytosol. However, the whole system did not work, in that the cells remained stuck indefinitely in their pro-inflamamtory start-up program. They concluded that this was due largely or entirely to the cells not having enough 25-hydroxyvitamin D. There were no observations of these patient's circulating 25-hydroxyvitamin D levels, but it is well established (see research cited at: https://vitamindstopscovid.info/00-evi/) that those who suffer the worst outcomes with COVID-19 are, in general, those with the lowest 25-hydroxyvitamin D levels.
These people were hospitalised due to the virus getting into their lungs, rather than being stopped at the upper respiratory stage, which is what would normally occur if the immune system was working properly. In the lungs, most of the damage follows from the inflammatory immune responses, which damage endothelial cells there (those which line the blood vessels and capillaries, particulary in the oxygen and carbon dioxide exchange air sacs - alveoli). The body responds to the damaged blood vessels as if there was an injury, with loss of blood by making the blood hyper-coagulatory in an effort to plug the leaks. This hyper-coagulatory blood does most of the final harm, by causing micro-embolisms and larger clots in all organs: the lungs, heart, liver, kidneys, brain and spinal cord. The resulting organ damage and/or lack of oxygen, due to impaired exchange in the alveoli, especially due to these being flooded with fluid, is what kills most COVID-19 patients.
This cascade would never occur in most people if they had 50 ng/mL or more circulating 25-hydroxyvitamin D. Without proper vitamin D3 supplementation, most people have only a fraction of this, 1/10th to 1/2. So their immune systems cannot function properly. (There is very little vitamin D3 in food or multivitamins. It can be produced by UV-B irradiation of ideally white skin, but this is impossible for most people to obtain all year round, and it always damages DNA and so raises the risk of skin cancer.)
In clinical emergencies such as this, most doctors have no idea that lack of 25-hydroxyvitamin D is an easily correctable deficiency which must be reversed immediately. This is because they have never heard of 25-hydroxyvitamin D -> calcitriol intracrine signaling in immune cells. (A related paracrine signaling system involves some of the intracellularly produce calcitriol diffusing to nearby cells, where it affects their behaviour.)
No amount of vitamin C or any other treatment can compensate for the patient's 25-hydroxyvitamin D level being far below 50 ng/mL.
Supplementing ordinary healthy quantities of vitamin D3 (see Prof. Sunil Wimalawansa's recommendations: https://vitamindstopscovid.info/00-evi/#00-how-much) such as 0.125 mg (5000 IU) a day will raise 25-hydroxyvitamin D levels to 50 ng/mL, but this takes two months or so.
A loading (bolus = single, very large) dose of vitamin D3 such as 10 mg 400,000 IU for average weight adults will boost the 25-hydroxyvitamin D level over 50 ng/mL over several days. The delay is due to how long it takes the liver to hydroxylate it, with about 1/4 of the supplied vitamin D molecules becoming circulating 25-hydroxyvitamin D.
This treatment could have saved the lives of most of those who died from COVID-19, but there is a still better treatment: oral calcifediol.
For an average weight adult, 1 milligram of oral calcifediol (which _is_ 25-hydroxyvitamin D), raises the level of circulating 25-hydroxyvitamin D safely over 50 ng/mL in 4 hours or less. 25-hydroxyvitamin D is more easily absorbed than vitamin D3 since it has two hydrophilic hydroxyl groups,while vitamin D3 has only one. The calcifediol is well absorbed and goes straight into circulation.
Unfortunately, except in Spain, Italy and a few nearby countries, it is difficult for doctors to obtain calcifediol by the milligram. See the stunning success of this treatment in Castillo et al. 2020, cited and discussed at: https://vitamindstopscovid.info/00-evi/#castillo. Every doctor in the world should have known about this by late 2020.
This would have been an even more effective treatment for COVID-19 than bolus vitamin D3, since some of these hospitalised patients were fighting for their lives, and didn't have a few days to wait for bolus vitamin D3 to boost their circulating 25-hydroxyvitamin D level.
While the FLCCC COVID-19 protocols do recommend this calcifediol treatment (0.014 mg per kg body weight) with bolus vitamin D3 if this is not available, the FLCCC's sepsis protocol does not mention vitamin D.
Low 25-hydroxyvitamin D is the primary avoidable cause of the extreme weakness of desirable immune responses in sepsis and of the dysregulated, self-destructive, very high levels of cell-destroying inflammation which characterises this often deadly condition. Sepsis killed about 11 million people, worldwide, in 2017: https://www.thelancet.com/ journals/lancet/article/PIIS0140-6736(19)32989-7/ .
Please also see the research cited at: https://vitamindstopscovid.info/06-adv/ which shows that most people in developed countries, who are not infested with intestinal worms (helminths) have more intense, likely self-destructive, inflammatory responses, since helminths evolved compounds to downmodulate these responses which target them, and our ancestor's immune systems evolved to have stronger and stronger inflammatory responses, in an effort to counter the effects of ubiquitous infestation with one or more species of helminth.
(1 of 2) Please see the research articles concerning the vitamin D compounds and the immune system, cited and discussed at https://vitamindstopscovid.info/00-evi/ for the background to all that follows.
Sepsis would be rare if everyone had at least the 50 ng/mL (125 nmol/L = 1 part in 20,000,000 by mass) circulating 25-hydroxyvitamin D their immune systems need to function properly. 25-hydroxyvitamin D calcifediol (AKA "calcidiol") is produced, mainly in the liver, over several days, from ingested or UV-B -> skin produced vitamin D3 cholecalciferol. "Vitamin D" blood tests measure the level (concentration) of 25-hydroxyvitamin D in the bloodstream, where it has a half life of weeks to a month or two.
Neither of these compounds function as hormones (long distance signaling molecules in the bloodstream). They are not signaling molecules. Vitamin D3's primary role is to be hydroxylated at the 25th carbon to 25-hydroxyvitamin D. 25 hydroxyvitamin D's best known role is to supply the kidneys, so they can hydroxylate it at the 1st carbon to become 1,25-dihydroxyvitamin D calcitriol. This goes into circulation at a very low level, ca. 0.05 to 0.1 ng/mL, where it functions as a hormone, affecting the behaviour of multiple cell types all around the body which are involved in calcium-phosphate-bone metabolism. The kidney's rate of hydroxylation depends on the parathyroid hormone (the parathyroid senses the bloods concentration of calcium ions, which must be controlled within very narrow limits) and by FGF-23 (fibroblast growth factor), which functions as a hormone, which is emitted by osteocytes.
It is often said that "vitamin D" is a hormone, but only calcitriol can act as a hormone, and this is a different compound from vitamin D3 and 25-hydroxyvitamin D. All the other functions of calcitriol, which are not well known, even to immunologists, are non-hormonal - as an intracrine agent or paracrine agent. These roles involve signaling within a single cell, or to nearby cells.
Hardly known at all to medical professionals and researchers, calcitriol also functions as a signaling molecule within individual cells, including many types of immune cell. This is intracrine signaling, which enables the cell to respond to its individual circumstances. In order for this to work properly, 25-hydroxyvitamin D needs to diffuse into the cell from the bloodstream. It appears that this can only occur to the degree necessary for full operation of the intracrine signaling systems if the level in the blood is 50 ng/mL or more.
Intracrine signaling is a general principle. Here is how it works for 25-hydroxyvitamin D -> calcitriol intracrine signaling, in this example, in Th1 regulatory lymphocytes, as elucidated in 2021 by Chauss et al. https://www.nature.com/articles/s41590-021-01080-3. (A summary of this dense cell-biology article is at: https://aminotheory.com/cv19/icu/#2021-Chauss.) They incorrectly referred to this as "autocrine" signaling, in which the receptor for the signaling molecule is on the outside of the cell, but it is inside the cell, in the cytosol, which is properly known as intracrine signaling.
The cell detects a cell-type specific external or internal condition. In the case of Th1 cells, this is the presence, outside the cell, of a high level of a particular complement protein. (Complement is a set of proteins which are important in blood clotting.) This causes the cell to produce two molecules in its cytosol: the 1-hydroxylase enzyme and the so-called "vitamin D receptor" (VDR). The VDR molecule has a low affinity for vitamin D3 and 25-hydroxyvitamin D, but a very high affinity for calcitriol. It is best to think of it as the "calcitriol receptor".
Assuming there is sufficient 25-hydroxyvitamin D in the cytosol, with more diffusing in as the following process occurs, the enzyme hydroxylates these molecules to become calcitriol. Each molecule of calcitriol binds tightly to a VDR molecule and the bound complexes find their way (by diffusion, to the best of my knowledge) into the nucleus where they bind to another molecule, retinol-X. The triple complex then alters the transcription of genes in the cell's DNA into messenger RNA molecules. This is a subtle and complex process, and the outcome is different for each kind of cell. Dozens to hundreds of genes are up-regulated - more copies of these are made to mRNA molecules than before. Dozens to hundreds of genes are down-regulated, so there are fewer mRNA copies than before. The details of which genes these are vary from one cell type to the next, as does the initial condition wich started this intracrine signaling process. mRNA molecules diffuse from the nucleus to the cytosol, where they program ribosomes to produce protein. Each mRNA carries the instructions to make one type of protein. (The details are more complex, since the mRNA can be edited before getting to the ribosomes.)
Th1 cells emit cytokines - short distance signaling molecules which affect the behaviour or one or more types of immune cells. Their startup program is for the cell to emit more (in terms of their effects) of a pro-inflammatory cytokine than of an anti-inflammatory cytokine.
"Inflammatory", in this context, means that certain types of immune cells, such as eosinophils (the suicide bombers of the immune system) destroy all types of cell, ideally those of pathogens, but also, inevitably, our own cells. These inflammatory responses evolved primarily to deal with multicellular parasites such as intestinal worms, which are not affected by other immune responses, such as antibodies and macrophages.
When Th1 cells detect the high level of the complement protein, and have sufficient 25-hydroxyvitamin D to run their intracrine signaling system, they produce, inside the cell, sufficient calcitriol to change the cell's behaviour by turning off its pro-inflammatory startup program and switching the cell to its anti-inflammatory shutdown program, in which it produces, and so releases to surrounding cells, less of the pro-inflammatory cytokine and more of the anti-inflammatory cytokine.
daily IRD dose of vitC is 50mg, just enough not to die....(Codex Alimentarius)
The Samoa measles outbreak in 2019 characterized by a door-door mandatory vaccination (deaths 1 in 64..) was proceeded by RF Kennedy's visit who collaborated with a local who was administering 1-2 g VitC every 2 h PLUS 100,000 Vit A (extremely important for EYES!!) for 3 days in total, making the dying children to 'wake up' literally within few hours of administration.... That individual was sued later on and RFKennedy accused of 'killing' people.. It was possible that this case was the first test ground for covid vaccines mixed up with measles vaccines, causing the massive deaths...
A great Dr. Thomas Lodi, natural practitioner is taking 50,000 IU of Vit A day himslef...
Oh it was planned, but not by GOF which is yet another ruse to cause mass formation hysteria. It was planned by creating the most corrupt medical test protocol ever devised. Known as Corman Drosten for the two primary developers of the protocol. A massive false positive generator through manipulated molecular chemistry and lab methodology. High sensitivity and no specificity built into the protocol. A professional peer review group did a point by point examination of the molecular chemistry and methods used in the labs worldwide, compared them to the best knowledge on PCR testing and concluded the test was worthless as a medical diagnostic test. Yet it was the overwhelmingly most used test around the world for the identification of SARScoV2. See the Corman Drosten Review report online. PU.
Hi Steve, just a note to address a few items, number 1. Thank you for being brave during the hardest times in modern history. Your data and stats just couldn’t be denied and still can’t be. Numbers and documented facts are definitely the bullets that won the disinformation and propaganda blasted by the medical industrial complex, the NIH, WHO,and so on. Now that we will have a powerhouse of Individuals in the White House and the new cabinet that know the facts…. There will be a cleansing! You are a brave man and we thank you. I have a personal request, now that your friend Jay is top man and RFK Jr. have President Trump’s ear, could you please ask him to review the plight of Dr. Reiner Fullemich who is sitting in a jail cell in solitary confinement and has not yet been charged with a crime. So many of the most knowledgeable medical experts on the planet made submissions to his Grand Jury presentation on Covid. Could you have some kind of contact through the two aforementioned experts to get something done to have Reiner released. This is a great injustice to a wonderful altruistic soul. Many thanks on behalf of those who trusted his information and did not fold to the demands of those pushing the wrong narrative during the Crazy Years.
Clever experiments in Healthy Human Volunteers in 1988 showed Endotoxin causes immediate increased Intestinal Permeability. How many people suffer Permanent Gut Damage after Covid19 Jabs?
Sepsis can happen so fast...learning the first warning signs is imperative. Know the symptoms such as changed temperature, changed breathing, heart rate...
Always listen to your body...antibiotics can treat sepsis if you catch it early.
The better you get at listening to your body and what it's telling you, the better chances you have at healing it. Our bodies are pretty magical. They talk to us with signs and warnings when something is going awry. Listen to your body, love your body...and you will figure out ways to cure and heal yourself.
"the sky-rocking number of sepsis cases occurring throughout the world, and discuss what, if any, connection this disturbing trend may have with C19 disease and its associated injectables. "
There's a lot to unpack there.
I am glad that I live in the last vestiges of my beloved USA where we can discuss subjects such as this.
I am glad I live in the USA where I probably won't be arrested for saying..."Reasonable people can disagree where "C19 disease" is a thing, is a "disease," and is a "diagnosis of a disease."
Thanks Steve for all you have done and are doing to enlighten others to what is truly going on. People have given up on anything of value coming from TV and newspapers.
I know of a late 40's vxxxd female in excellent health with a "cut" that reportedly became infected, she developed sepsis. Lost one leg and I heard both hands were in danger of being amputated. No one mentioned mRNA injections and their adverse affects on the immune system.
Glad to hear Steve has cut sugar out. Don't forget to consume enough healthy fat and water. It will solve any sluggish digestive issues.
Dr. Geert Vanden Bossche is still trying to defend his tribe of vaccinologists by being luke-warm on Bobby and by accepting "not-perfect" MMR & Dtap vaccines. At least he rejects all other vaccines, including polio and Covid.
He is right when he says CLEAN WATER is more important and the vaccine-derived polio is worse than wild polio.
Wow, thousands and thousands of people should be hearing this and reading the comments, and I cannot believe that only 98 have liked it, and 23 responded? If that isn't proof of suppression and censorship, then I don't know what else to tell you...carry on, faithful soldier!
Most likely this is not a reflection of who has viewed this.
(2 of 2) Chauss et al. studied Th1 cells from the lungs of hospitalised COVID-19 patients.
They found that the cells' intracine signaling system was being activated as it should be, with the 1-hydroxlase enzyme and VDR being produced in the cytosol. However, the whole system did not work, in that the cells remained stuck indefinitely in their pro-inflamamtory start-up program. They concluded that this was due largely or entirely to the cells not having enough 25-hydroxyvitamin D. There were no observations of these patient's circulating 25-hydroxyvitamin D levels, but it is well established (see research cited at: https://vitamindstopscovid.info/00-evi/) that those who suffer the worst outcomes with COVID-19 are, in general, those with the lowest 25-hydroxyvitamin D levels.
These people were hospitalised due to the virus getting into their lungs, rather than being stopped at the upper respiratory stage, which is what would normally occur if the immune system was working properly. In the lungs, most of the damage follows from the inflammatory immune responses, which damage endothelial cells there (those which line the blood vessels and capillaries, particulary in the oxygen and carbon dioxide exchange air sacs - alveoli). The body responds to the damaged blood vessels as if there was an injury, with loss of blood by making the blood hyper-coagulatory in an effort to plug the leaks. This hyper-coagulatory blood does most of the final harm, by causing micro-embolisms and larger clots in all organs: the lungs, heart, liver, kidneys, brain and spinal cord. The resulting organ damage and/or lack of oxygen, due to impaired exchange in the alveoli, especially due to these being flooded with fluid, is what kills most COVID-19 patients.
This cascade would never occur in most people if they had 50 ng/mL or more circulating 25-hydroxyvitamin D. Without proper vitamin D3 supplementation, most people have only a fraction of this, 1/10th to 1/2. So their immune systems cannot function properly. (There is very little vitamin D3 in food or multivitamins. It can be produced by UV-B irradiation of ideally white skin, but this is impossible for most people to obtain all year round, and it always damages DNA and so raises the risk of skin cancer.)
In clinical emergencies such as this, most doctors have no idea that lack of 25-hydroxyvitamin D is an easily correctable deficiency which must be reversed immediately. This is because they have never heard of 25-hydroxyvitamin D -> calcitriol intracrine signaling in immune cells. (A related paracrine signaling system involves some of the intracellularly produce calcitriol diffusing to nearby cells, where it affects their behaviour.)
No amount of vitamin C or any other treatment can compensate for the patient's 25-hydroxyvitamin D level being far below 50 ng/mL.
Supplementing ordinary healthy quantities of vitamin D3 (see Prof. Sunil Wimalawansa's recommendations: https://vitamindstopscovid.info/00-evi/#00-how-much) such as 0.125 mg (5000 IU) a day will raise 25-hydroxyvitamin D levels to 50 ng/mL, but this takes two months or so.
A loading (bolus = single, very large) dose of vitamin D3 such as 10 mg 400,000 IU for average weight adults will boost the 25-hydroxyvitamin D level over 50 ng/mL over several days. The delay is due to how long it takes the liver to hydroxylate it, with about 1/4 of the supplied vitamin D molecules becoming circulating 25-hydroxyvitamin D.
This treatment could have saved the lives of most of those who died from COVID-19, but there is a still better treatment: oral calcifediol.
For an average weight adult, 1 milligram of oral calcifediol (which _is_ 25-hydroxyvitamin D), raises the level of circulating 25-hydroxyvitamin D safely over 50 ng/mL in 4 hours or less. 25-hydroxyvitamin D is more easily absorbed than vitamin D3 since it has two hydrophilic hydroxyl groups,while vitamin D3 has only one. The calcifediol is well absorbed and goes straight into circulation.
Unfortunately, except in Spain, Italy and a few nearby countries, it is difficult for doctors to obtain calcifediol by the milligram. See the stunning success of this treatment in Castillo et al. 2020, cited and discussed at: https://vitamindstopscovid.info/00-evi/#castillo. Every doctor in the world should have known about this by late 2020.
This would have been an even more effective treatment for COVID-19 than bolus vitamin D3, since some of these hospitalised patients were fighting for their lives, and didn't have a few days to wait for bolus vitamin D3 to boost their circulating 25-hydroxyvitamin D level.
While the FLCCC COVID-19 protocols do recommend this calcifediol treatment (0.014 mg per kg body weight) with bolus vitamin D3 if this is not available, the FLCCC's sepsis protocol does not mention vitamin D.
Low 25-hydroxyvitamin D is the primary avoidable cause of the extreme weakness of desirable immune responses in sepsis and of the dysregulated, self-destructive, very high levels of cell-destroying inflammation which characterises this often deadly condition. Sepsis killed about 11 million people, worldwide, in 2017: https://www.thelancet.com/ journals/lancet/article/PIIS0140-6736(19)32989-7/ .
Please also see the research cited at: https://vitamindstopscovid.info/06-adv/ which shows that most people in developed countries, who are not infested with intestinal worms (helminths) have more intense, likely self-destructive, inflammatory responses, since helminths evolved compounds to downmodulate these responses which target them, and our ancestor's immune systems evolved to have stronger and stronger inflammatory responses, in an effort to counter the effects of ubiquitous infestation with one or more species of helminth.
(1 of 2) Please see the research articles concerning the vitamin D compounds and the immune system, cited and discussed at https://vitamindstopscovid.info/00-evi/ for the background to all that follows.
Sepsis would be rare if everyone had at least the 50 ng/mL (125 nmol/L = 1 part in 20,000,000 by mass) circulating 25-hydroxyvitamin D their immune systems need to function properly. 25-hydroxyvitamin D calcifediol (AKA "calcidiol") is produced, mainly in the liver, over several days, from ingested or UV-B -> skin produced vitamin D3 cholecalciferol. "Vitamin D" blood tests measure the level (concentration) of 25-hydroxyvitamin D in the bloodstream, where it has a half life of weeks to a month or two.
Neither of these compounds function as hormones (long distance signaling molecules in the bloodstream). They are not signaling molecules. Vitamin D3's primary role is to be hydroxylated at the 25th carbon to 25-hydroxyvitamin D. 25 hydroxyvitamin D's best known role is to supply the kidneys, so they can hydroxylate it at the 1st carbon to become 1,25-dihydroxyvitamin D calcitriol. This goes into circulation at a very low level, ca. 0.05 to 0.1 ng/mL, where it functions as a hormone, affecting the behaviour of multiple cell types all around the body which are involved in calcium-phosphate-bone metabolism. The kidney's rate of hydroxylation depends on the parathyroid hormone (the parathyroid senses the bloods concentration of calcium ions, which must be controlled within very narrow limits) and by FGF-23 (fibroblast growth factor), which functions as a hormone, which is emitted by osteocytes.
It is often said that "vitamin D" is a hormone, but only calcitriol can act as a hormone, and this is a different compound from vitamin D3 and 25-hydroxyvitamin D. All the other functions of calcitriol, which are not well known, even to immunologists, are non-hormonal - as an intracrine agent or paracrine agent. These roles involve signaling within a single cell, or to nearby cells.
Hardly known at all to medical professionals and researchers, calcitriol also functions as a signaling molecule within individual cells, including many types of immune cell. This is intracrine signaling, which enables the cell to respond to its individual circumstances. In order for this to work properly, 25-hydroxyvitamin D needs to diffuse into the cell from the bloodstream. It appears that this can only occur to the degree necessary for full operation of the intracrine signaling systems if the level in the blood is 50 ng/mL or more.
Intracrine signaling is a general principle. Here is how it works for 25-hydroxyvitamin D -> calcitriol intracrine signaling, in this example, in Th1 regulatory lymphocytes, as elucidated in 2021 by Chauss et al. https://www.nature.com/articles/s41590-021-01080-3. (A summary of this dense cell-biology article is at: https://aminotheory.com/cv19/icu/#2021-Chauss.) They incorrectly referred to this as "autocrine" signaling, in which the receptor for the signaling molecule is on the outside of the cell, but it is inside the cell, in the cytosol, which is properly known as intracrine signaling.
The cell detects a cell-type specific external or internal condition. In the case of Th1 cells, this is the presence, outside the cell, of a high level of a particular complement protein. (Complement is a set of proteins which are important in blood clotting.) This causes the cell to produce two molecules in its cytosol: the 1-hydroxylase enzyme and the so-called "vitamin D receptor" (VDR). The VDR molecule has a low affinity for vitamin D3 and 25-hydroxyvitamin D, but a very high affinity for calcitriol. It is best to think of it as the "calcitriol receptor".
Assuming there is sufficient 25-hydroxyvitamin D in the cytosol, with more diffusing in as the following process occurs, the enzyme hydroxylates these molecules to become calcitriol. Each molecule of calcitriol binds tightly to a VDR molecule and the bound complexes find their way (by diffusion, to the best of my knowledge) into the nucleus where they bind to another molecule, retinol-X. The triple complex then alters the transcription of genes in the cell's DNA into messenger RNA molecules. This is a subtle and complex process, and the outcome is different for each kind of cell. Dozens to hundreds of genes are up-regulated - more copies of these are made to mRNA molecules than before. Dozens to hundreds of genes are down-regulated, so there are fewer mRNA copies than before. The details of which genes these are vary from one cell type to the next, as does the initial condition wich started this intracrine signaling process. mRNA molecules diffuse from the nucleus to the cytosol, where they program ribosomes to produce protein. Each mRNA carries the instructions to make one type of protein. (The details are more complex, since the mRNA can be edited before getting to the ribosomes.)
Th1 cells emit cytokines - short distance signaling molecules which affect the behaviour or one or more types of immune cells. Their startup program is for the cell to emit more (in terms of their effects) of a pro-inflammatory cytokine than of an anti-inflammatory cytokine.
"Inflammatory", in this context, means that certain types of immune cells, such as eosinophils (the suicide bombers of the immune system) destroy all types of cell, ideally those of pathogens, but also, inevitably, our own cells. These inflammatory responses evolved primarily to deal with multicellular parasites such as intestinal worms, which are not affected by other immune responses, such as antibodies and macrophages.
When Th1 cells detect the high level of the complement protein, and have sufficient 25-hydroxyvitamin D to run their intracrine signaling system, they produce, inside the cell, sufficient calcitriol to change the cell's behaviour by turning off its pro-inflammatory startup program and switching the cell to its anti-inflammatory shutdown program, in which it produces, and so releases to surrounding cells, less of the pro-inflammatory cytokine and more of the anti-inflammatory cytokine.
daily IRD dose of vitC is 50mg, just enough not to die....(Codex Alimentarius)
The Samoa measles outbreak in 2019 characterized by a door-door mandatory vaccination (deaths 1 in 64..) was proceeded by RF Kennedy's visit who collaborated with a local who was administering 1-2 g VitC every 2 h PLUS 100,000 Vit A (extremely important for EYES!!) for 3 days in total, making the dying children to 'wake up' literally within few hours of administration.... That individual was sued later on and RFKennedy accused of 'killing' people.. It was possible that this case was the first test ground for covid vaccines mixed up with measles vaccines, causing the massive deaths...
A great Dr. Thomas Lodi, natural practitioner is taking 50,000 IU of Vit A day himslef...
For stress and diabetes, extremely important:
https://staging1.stetzerelectric.com/wp-content/uploads/Milham-Stetzer-2013-Dirty-electricity-chronic-stress-neurotransmitters-and-disease.pdf
In terms of Vit C Dr. Thomas Levy is also great resource, here some of it:
http://www.rvr.medfoxpub.com [ Rapid Virus Recovery ], Book (over 190,000 downloads and counting)
http://orthomolecular.org/resources/omns/v17n13.shtml ("Hydrogen Peroxide Nebulization and COVID Resolution")
http://orthomolecular.org/resources/omns/v18n18.shtml ("Hospital Study Shows that COVID-19 can be Prevented with Hydrogen Peroxide")
http://orthomolecular.org/resources/omns/v17n24.shtml ("Canceling the Spike Protein: Striking Visual Evidence")
http://orthomolecular.org/resources/omns/v17n28.shtml ("Vitamin C and Cortisol: Synergistic Infection and Toxin Defense")
http://orthomolecular.org/resources/omns/v18n06.shtml ("How COVID Helped Me Regain Good Health")
http://orthomolecular.org/resources/omns/v18n14.shtml ("The Restoration of Vitamin C Synthesis in Humans")
http://orthomolecular.org/resources/omns/v18n17.shtml (“Monkeypox Infection: To Fear or not to Fear?”)
http://orthomolecular.org/resources/omns/v18n24.shtml ("Atherosclerosis is a Non-Healing Wound")
http://orthomolecular.org/resources/omns/v19n01.shtml ("Myocarditis: Once Rare, Now Common")
http://orthomolecular.org/resources/omns/v19n08.shtml ("Resolving Colds to Advanced COVID with Methylene Blue")
http://orthomolecular.org/resources/omns/v19n15.shtml ("Resolving Persistent Spike Protein Syndrome")
http://orthomolecular.org/resources/omns/v19n36.shtml ("The Toxic Nutrient Triad")
http://orthomolecular.org/resources/omns/v19n39.shtml ("Persistent Spike Protein Syndrome: Rapid Resolution with Ultraviolet Blood Irradiation")
http://orthomolecular.org/resources/omns/v19n40.shtml ("Schizophrenia Is Chronic Encephalitis...And Niacin Cures it")
http://orthomolecular.org/resources/omns/v19n41.shtml ("Heart failure or therapy failure? Toxins Cause Cardiomyopathy")
http://orthomolecular.org/resources/omns/v19n45.shtml (“Root Canals Cause Breast Cancer-- Frequently ”)
http://www.dbc2.medfoxpub.com [ Death by Calcium ], Book
covid is a plandemic with illegal gain of function research. See science facts on makingsenseocovid.com
Oh it was planned, but not by GOF which is yet another ruse to cause mass formation hysteria. It was planned by creating the most corrupt medical test protocol ever devised. Known as Corman Drosten for the two primary developers of the protocol. A massive false positive generator through manipulated molecular chemistry and lab methodology. High sensitivity and no specificity built into the protocol. A professional peer review group did a point by point examination of the molecular chemistry and methods used in the labs worldwide, compared them to the best knowledge on PCR testing and concluded the test was worthless as a medical diagnostic test. Yet it was the overwhelmingly most used test around the world for the identification of SARScoV2. See the Corman Drosten Review report online. PU.
Hi Steve, just a note to address a few items, number 1. Thank you for being brave during the hardest times in modern history. Your data and stats just couldn’t be denied and still can’t be. Numbers and documented facts are definitely the bullets that won the disinformation and propaganda blasted by the medical industrial complex, the NIH, WHO,and so on. Now that we will have a powerhouse of Individuals in the White House and the new cabinet that know the facts…. There will be a cleansing! You are a brave man and we thank you. I have a personal request, now that your friend Jay is top man and RFK Jr. have President Trump’s ear, could you please ask him to review the plight of Dr. Reiner Fullemich who is sitting in a jail cell in solitary confinement and has not yet been charged with a crime. So many of the most knowledgeable medical experts on the planet made submissions to his Grand Jury presentation on Covid. Could you have some kind of contact through the two aforementioned experts to get something done to have Reiner released. This is a great injustice to a wonderful altruistic soul. Many thanks on behalf of those who trusted his information and did not fold to the demands of those pushing the wrong narrative during the Crazy Years.
Long live Reiner Fullemich!!!! PU.
Clever experiments in Healthy Human Volunteers in 1988 showed Endotoxin causes immediate increased Intestinal Permeability. How many people suffer Permanent Gut Damage after Covid19 Jabs?
https://geoffpain.substack.com/p/leaky-gut-caused-by-endotoxin-in
I had the pleasure of meeting Dr Paul Marik in his recent visit to Australia.
You might like
https://geoffpain.substack.com/p/endotoxin-reference-deleted-in-ukhsa
Sepsis can happen so fast...learning the first warning signs is imperative. Know the symptoms such as changed temperature, changed breathing, heart rate...
Always listen to your body...antibiotics can treat sepsis if you catch it early.
The better you get at listening to your body and what it's telling you, the better chances you have at healing it. Our bodies are pretty magical. They talk to us with signs and warnings when something is going awry. Listen to your body, love your body...and you will figure out ways to cure and heal yourself.
Listen to the signs...don't ignore them.
"the sky-rocking number of sepsis cases occurring throughout the world, and discuss what, if any, connection this disturbing trend may have with C19 disease and its associated injectables. "
There's a lot to unpack there.
I am glad that I live in the last vestiges of my beloved USA where we can discuss subjects such as this.
I am glad I live in the USA where I probably won't be arrested for saying..."Reasonable people can disagree where "C19 disease" is a thing, is a "disease," and is a "diagnosis of a disease."
Thanks Steve for all you have done and are doing to enlighten others to what is truly going on. People have given up on anything of value coming from TV and newspapers.
UNITE WITH GOD, PRAY AND PREP
When I was a young kid, The Blob scared us saying the Earth was going to freeze over. IIRC Carl Sagan even did a show on the great freezing.
Yes. How ridiculous we humans are.