We demonstrated in 1985 that vanadium administered in the drinking water to streptozotocin (STZ) diabetic rats restored elevated blood glucose to normal. Subsequent studies have shown that vanadyl sulfate can lower elevated blood glucose, cholesterol and triglycerides in a variety of diabetic models including the STZ diabetic rat, the Zucker fatty rat and the Zucker diabetic fatty rat. Long-term studies of up to one year did not show toxicity in control or STZ rats administered vanadyl sulfate in doses that lowered elevated blood glucose. In the BB diabetic rat, a model of insulin-dependent diabetes, vanadyl sulfate lowered the insulin requirement by up to 75%. Vanadyl sulfate is effective orally when administered by either single dose or chronic doses. It is also effective by the intraperitoneal route. We have also been able to demonstrate marked long-term effects of vanadyl sulfate in diabetic animals following treatment and withdrawal of vanadyl sulfate. Because vanadyl sulfate is not well absorbed we have synthesized and tested a number of organic vanadium compounds. One of these, bismaltolato-oxovanadium IV (BMOV), has shown promise as a therapeutic agent. BMOV is 2-3x more potent than vanadyl sulfate and has shown less toxicity. Recent studies from our laboratory have shown that the effects of vanadium are not due to a decrease in food intake and that while vanadium is deposited in bone it does not appear to affect bone strength or architecture. The mechanism of action of vanadium is currently under investigation. Several studies indicate that vanadium is a phosphatase inhibitor and that vanadium can activate serine/threonine kinases distal to the insulin receptor presumably by preventing dephosphorylation due to inhibition of phosphatases Short-term clinical trials using inorganic vanadium compounds in diabetic patients have been promising."...
This was a massive study done on/to nearly 2,000 subjects, in China, further showing what has been known for over 30 fucking years, now: https://www.ncbi.nlm.nih.gov/pubmed/25005791
..."Analyses showed that plasma vanadium concentrations were significantly lower in cases with newly diagnosed type 2 diabetes than in controls (P = 0.001). Mean plasma vanadium levels in participants with and without diabetes were 1.0 μg/L and 1.2 μg/L, respectively. Participants in the highest quartile of plasma vanadium concentration had a notably lower risk of newly diagnosed type 2 diabetes (odds ratio = 0.26, 95% confidence interval: 0.19, 0.35; P < 0.001), compared with persons in the lowest quartile. The trend remained significant after adjustment for known risk factors and in further stratification analyses. Our results suggested that plasma vanadium concentrations were inversely associated with newly diagnosed type 2 diabetes in this Chinese population."...
I can go on and on, but the OBVIOUS reason that this amazing information is suppressed is blatantly-obvious, and it should be a fucking crime that this information, and the use-of-vanadium, is being intentionally-suppressed.
This is an actual protocol that has been used, but, again, I iterate, that you MUST consult with your physician, before beginning any protocol with vanadium, but this is the real deal, and I only hope that you do not ignore what I am presenting to you: http://whale.to/a/diabetes_shame.html
This is the prima-facie-evidence of regeneration-of-tissue, using vanadium, which, over-time, makes the islets-of-langerhans begin producing insulin, again: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4156977/
"Abstract
We examined the effects of vanadium sulfate (VOSO4) treatment at 5 and 10 mg/kg for 30 days on endocrine pancreas activity and histology in nondiabetic and STZ-induced diabetic rats. In diabetic group, blood glucose levels significantly increased while insulinemia level markedly decreased. At the end of treatment, VOSO4 at a dose of 10 mg/Kg normalized blood glucose level in diabetic group, restored insulinemia, and significantly improved insulin sensitivity. VOSO4 also increased in a dose-dependent manner the number of insulin immunopositive beta cells in pancreatic islets of nondiabetic rats. Furthermore, in the STZ-diabetic group, the decrease in the number of insulin immunopositive beta cells was corrected to reach the control level mainly with the higher dose of vanadium. Therefore, VOSO4 treatment normalized plasma glucose and insulin levels and improved insulin sensitivity in STZ-experimental diabetes and induced beta cells proliferation and/or regeneration in normal or diabetic rats."...
For-the-record, the best treatment, and, what MANY people call a "cure", for the vast majority-of-subjects, for diabetes, particularly "type 2", but primary-diabetes is treatable with it, is very, very simple: vanadium, particularly found as vanadium-sulfate, but there is a much less-toxic form, known as "VMOS", which your physician and you need to discuss.
You will have to consult with your physician, to have him help create a personal protocol for you, since it is not recommended to reverse the disease by one-self, since you have to know how well the organ, islets-of-langerhans, which is found ON-TOP-OF the pancreas, and not the pancreas, itself, is progressing, but, for the vast majority of subjects, the organ should be healthy-enough for active-function, within two to four months, after which time, the diseased-condition is reversed.
I should have shared this knowledge with you, before now, but it is done, regardless-of-anything.
What I can tell you, for sure, is to not take more than 100 mcg, per-day, since at that dose, the effect-on-blood-sugar can be too "good"/extreme, so just remember that, and know that the supplement can be VERY EASILY bought at Puritan.com , along with almost any other pill-form supplement that a subject would want/need.
Here is the first white-paper confirming that vanadium sulphate reverses the disease, confirmed firstly, in 1985, and re-confirmed, definitively, in 1998: https://www.researchgate.net/publication/227120683_Vanadium_and_diabetes
"Abstract We demonstrated in 1985 that vanadium administered in the drinking water to streptozotocin (STZ) diabetic rats restored elevated blood glucose to normal. Subsequent studies have shown that vanadyl sulfate can lower elevated blood glucose, cholesterol and triglycerides in a variety of diabetic models including the STZ diabetic rat, the Zucker fatty rat and the Zucker diabetic fatty rat. Long-term studies of up to one year did not show toxicity in control or STZ rats administered vanadyl sulfate in doses that lowered elevated blood glucose. In the BB diabetic rat, a model of insulin-dependent diabetes, vanadyl sulfate lowered the insulin requirement by up to 75%. Vanadyl sulfate is effective orally when administered by either single dose or chronic doses. It is also effective by the intraperitoneal route. We have also been able to demonstrate marked long-terrn effects of vanadyl sulfate in diabetic animals following treatment and withdrawal of vanadyl sulfate. Because vanadyl sulfate is not well absorbed we have synthesized and tested a number of organic vanaditun compounds. One of these, bismaltolato-oxovanadiurn IV (BMOV), has shown promise as a therapeutic agent. BMOV is 2-3x more potent than vanadyl sulfate and has shown less toxicity. Recent studies from our laboratory have shown that the effects of vanadium are not due to a decrease in food intake and that while vanadium is deposited in bone it does not appear to affect bone strength or architecture. The mechanism of action of vanadium is currently under investigation. Several studies indicate that vanadiun is a phosphatase inhibitor and that vanadium can activate serine/threonine kineses distal to tbe insulin receptor presumably by preventing dephosphorylation due to inhibition of phosphatases Short-term clinical trials using inorganic vanadium compounds in diabetic patients have been promising."
This is another trial, basically proving the same fucking thing, written in 2012, ALREADY, proven, and verified, multiple times, decades before then, but, here it is, regardless: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3461829/
It's too intellectual for anyone in his twenties to have written it. ....like the question of whether a commoner of Stratford-on-Avon wrote all those plays and poems.
Hitler was born in 1889. He joined the Bavarian Army in 1914 (outbreak of WWI) at 25 years old. He dictated Mein Kampf to Rudolf Hess in 1925 at 35 years old.
Yes, and no, Mr. Millerman. The research is DEFINITIVE, as-far-as the effect-of-vanadium to reverse the condition is concerned--the only real problem was, IN-THE-PAST, limiting the toxic build-up-of-vanadium, which was, apparently, successfully done with the VMOS-form-of-the-metal.
Anyway, what I presented is an extremely promising start for ANYONE suffering from this terrible condition to begin a personalized-protocol-for-treatment, and -reversal, as MANY people have done, now, so this is real. It is equally-important to note that it is imperative that a physician works with the subject, as the subject MUST be aware of the progress being made, as well as any negative-effects, during treatment, which may manifest, like un-expected blood-sugar drops, especially.
For-the-record, I have had, at-least, two hypo-glycemic-attacks, due to my use of ALA--alpha-lipoic acid--and they were fully-fledged hypo-glycemic-attacks, with me nearly passing-out, and it was, all, because I had not eaten, and taken too-large-of-a-dose, over a period-of-time, which, on those two separate days, weeks/month apart, made my blood-sugar collapse, so, even a person with "perfect" blood-sugar-levels, like myself, can experience a severe hypo-glycemic-attack, using a supplement that is known to HELP diabetics. For-the-record, I was using ALA as an anti-oxidant, because it IS one of the most powerful anti-oxidants that there is.
https://www.ncbi.nlm.nih.gov/pubmed/9823013
ReplyDelete..."Abstract
We demonstrated in 1985 that vanadium administered in the drinking water to streptozotocin (STZ) diabetic rats restored elevated blood glucose to normal. Subsequent studies have shown that vanadyl sulfate can lower elevated blood glucose, cholesterol and triglycerides in a variety of diabetic models including the STZ diabetic rat, the Zucker fatty rat and the Zucker diabetic fatty rat. Long-term studies of up to one year did not show toxicity in control or STZ rats administered vanadyl sulfate in doses that lowered elevated blood glucose. In the BB diabetic rat, a model of insulin-dependent diabetes, vanadyl sulfate lowered the insulin requirement by up to 75%. Vanadyl sulfate is effective orally when administered by either single dose or chronic doses. It is also effective by the intraperitoneal route. We have also been able to demonstrate marked long-term effects of vanadyl sulfate in diabetic animals following treatment and withdrawal of vanadyl sulfate. Because vanadyl sulfate is not well absorbed we have synthesized and tested a number of organic vanadium compounds. One of these, bismaltolato-oxovanadium IV (BMOV), has shown promise as a therapeutic agent. BMOV is 2-3x more potent than vanadyl sulfate and has shown less toxicity. Recent studies from our laboratory have shown that the effects of vanadium are not due to a decrease in food intake and that while vanadium is deposited in bone it does not appear to affect bone strength or architecture. The mechanism of action of vanadium is currently under investigation. Several studies indicate that vanadium is a phosphatase inhibitor and that vanadium can activate serine/threonine kinases distal to the insulin receptor presumably by preventing dephosphorylation due to inhibition of phosphatases Short-term clinical trials using inorganic vanadium compounds in diabetic patients have been promising."...
This was a massive study done on/to nearly 2,000 subjects, in China, further showing what has been known for over 30 fucking years, now: https://www.ncbi.nlm.nih.gov/pubmed/25005791
..."Analyses showed that plasma vanadium concentrations were significantly lower in cases with newly diagnosed type 2 diabetes than in controls (P = 0.001). Mean plasma vanadium levels in participants with and without diabetes were 1.0 μg/L and 1.2 μg/L, respectively. Participants in the highest quartile of plasma vanadium concentration had a notably lower risk of newly diagnosed type 2 diabetes (odds ratio = 0.26, 95% confidence interval: 0.19, 0.35; P < 0.001), compared with persons in the lowest quartile. The trend remained significant after adjustment for known risk factors and in further stratification analyses. Our results suggested that plasma vanadium concentrations were inversely associated with newly diagnosed type 2 diabetes in this Chinese population."...
I can go on and on, but the OBVIOUS reason that this amazing information is suppressed is blatantly-obvious, and it should be a fucking crime that this information, and the use-of-vanadium, is being intentionally-suppressed.
The fuhrer's struggle is now our struggle sevenfold
DeleteThis is an actual protocol that has been used, but, again, I iterate, that you MUST consult with your physician, before beginning any protocol with vanadium, but this is the real deal, and I only hope that you do not ignore what I am presenting to you: http://whale.to/a/diabetes_shame.html
ReplyDeleteThis is the prima-facie-evidence of regeneration-of-tissue, using vanadium, which, over-time, makes the islets-of-langerhans begin producing insulin, again: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4156977/
"Abstract
We examined the effects of vanadium sulfate (VOSO4) treatment at 5 and 10 mg/kg for 30 days on endocrine pancreas activity and histology in nondiabetic and STZ-induced diabetic rats. In diabetic group, blood glucose levels significantly increased while insulinemia level markedly decreased. At the end of treatment, VOSO4 at a dose of 10 mg/Kg normalized blood glucose level in diabetic group, restored insulinemia, and significantly improved insulin sensitivity. VOSO4 also increased in a dose-dependent manner the number of insulin immunopositive beta cells in pancreatic islets of nondiabetic rats. Furthermore, in the STZ-diabetic group, the decrease in the number of insulin immunopositive beta cells was corrected to reach the control level mainly with the higher dose of vanadium. Therefore, VOSO4 treatment normalized plasma glucose and insulin levels and improved insulin sensitivity in STZ-experimental diabetes and induced beta cells proliferation and/or regeneration in normal or diabetic rats."...
Thank you so much, Oggie, for presenting this.
ReplyDeleteFor-the-record, the best treatment, and, what MANY people call a "cure", for the vast majority-of-subjects, for diabetes, particularly "type 2", but primary-diabetes is treatable with it, is very, very simple: vanadium, particularly found as vanadium-sulfate, but there is a much less-toxic form, known as "VMOS", which your physician and you need to discuss.
You will have to consult with your physician, to have him help create a personal protocol for you, since it is not recommended to reverse the disease by one-self, since you have to know how well the organ, islets-of-langerhans, which is found ON-TOP-OF the pancreas, and not the pancreas, itself, is progressing, but, for the vast majority of subjects, the organ should be healthy-enough for active-function, within two to four months, after which time, the diseased-condition is reversed.
I should have shared this knowledge with you, before now, but it is done, regardless-of-anything.
What I can tell you, for sure, is to not take more than 100 mcg, per-day, since at that dose, the effect-on-blood-sugar can be too "good"/extreme, so just remember that, and know that the supplement can be VERY EASILY bought at Puritan.com , along with almost any other pill-form supplement that a subject would want/need.
Here is the first white-paper confirming that vanadium sulphate reverses the disease, confirmed firstly, in 1985, and re-confirmed, definitively, in 1998: https://www.researchgate.net/publication/227120683_Vanadium_and_diabetes
"Abstract
We demonstrated in 1985 that vanadium administered in the drinking water to streptozotocin (STZ) diabetic rats restored elevated blood glucose to normal. Subsequent studies have shown that vanadyl sulfate can lower elevated blood glucose, cholesterol and triglycerides in a variety of diabetic models including the STZ diabetic rat, the Zucker fatty rat and the Zucker diabetic fatty rat. Long-term studies of up to one year did not show toxicity in control or STZ rats administered vanadyl sulfate in doses that lowered elevated blood glucose. In the BB diabetic rat, a model of insulin-dependent diabetes, vanadyl sulfate lowered the insulin requirement by up to 75%. Vanadyl sulfate is effective orally when administered by either single dose or chronic doses. It is also effective by the intraperitoneal route. We have also been able to demonstrate marked long-terrn effects of vanadyl sulfate in diabetic animals following treatment and withdrawal of vanadyl sulfate. Because vanadyl sulfate is not well absorbed we have synthesized and tested a number of organic vanaditun compounds. One of these, bismaltolato-oxovanadiurn IV (BMOV), has shown promise as a therapeutic agent. BMOV is 2-3x more potent than vanadyl sulfate and has shown less toxicity. Recent studies from our laboratory have shown that the effects of vanadium are not due to a decrease in food intake and that while vanadium is deposited in bone it does not appear to affect bone strength or architecture. The mechanism of action of vanadium is currently under investigation. Several studies indicate that vanadiun is a phosphatase inhibitor and that vanadium can activate serine/threonine kineses distal to tbe insulin receptor presumably by preventing dephosphorylation due to inhibition of phosphatases Short-term clinical trials using inorganic vanadium compounds in diabetic patients have been promising."
This is another trial, basically proving the same fucking thing, written in 2012, ALREADY, proven, and verified, multiple times, decades before then, but, here it is, regardless: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3461829/
Because I provided so much information, you will have to read it in-reverse-order, as I had to cut-and-paste, from the bottom, to the top.
ReplyDeletehttps://www.zerohedge.com/political/first-time-1934-hitlers-mein-kampf-be-reprinted-france
ReplyDelete
ReplyDeleteI don't think he wrote any of it.
It's too intellectual for anyone in his twenties to have written it. ....like the question of whether a commoner of Stratford-on-Avon wrote all those plays and poems.
..and a crap artist too?
Deleteits a great book
ReplyDeleteWoodrow:
ReplyDeleteHe was an excellent architectural painter and in watercolors, too!
Hitler was born in 1889. He joined the Bavarian Army in 1914 (outbreak of WWI) at 25 years old. He dictated Mein Kampf to Rudolf Hess in 1925 at 35 years old.
ReplyDeleteYes, and no, Mr. Millerman. The research is DEFINITIVE, as-far-as the effect-of-vanadium to reverse the condition is concerned--the only real problem was, IN-THE-PAST, limiting the toxic build-up-of-vanadium, which was, apparently, successfully done with the VMOS-form-of-the-metal.
ReplyDeleteAnyway, what I presented is an extremely promising start for ANYONE suffering from this terrible condition to begin a personalized-protocol-for-treatment, and -reversal, as MANY people have done, now, so this is real. It is equally-important to note that it is imperative that a physician works with the subject, as the subject MUST be aware of the progress being made, as well as any negative-effects, during treatment, which may manifest, like un-expected blood-sugar drops, especially.
For-the-record, I have had, at-least, two hypo-glycemic-attacks, due to my use of ALA--alpha-lipoic acid--and they were fully-fledged hypo-glycemic-attacks, with me nearly passing-out, and it was, all, because I had not eaten, and taken too-large-of-a-dose, over a period-of-time, which, on those two separate days, weeks/month apart, made my blood-sugar collapse, so, even a person with "perfect" blood-sugar-levels, like myself, can experience a severe hypo-glycemic-attack, using a supplement that is known to HELP diabetics. For-the-record, I was using ALA as an anti-oxidant, because it IS one of the most powerful anti-oxidants that there is.