We were using ARS ALB 30 in high dilutions even in infants, with the conviction that dilutions above avogadro limit will not contain any remains of original drug substance. That is why homeopathy was accepted as a SAFE medicine. Now, in their eagerness to become famous as ‘scientists’, our ‘homeopathic researchers’ are making theories to prove that potentized ARS ALB will contain ARSENIC NANOPARTICLES! And our ‘science-starved’ homeopath friends are celebrating these ‘researches’ as great achievements for homeopathy, saying that ‘detection of nanoparticles’ has ‘debunked’ the ‘placebo’ allegations against homeopathy! Actually, the ‘nanoparticle theory’ is debunking our claims about the ‘safety’ of homeopathy.
Are they working FOR homeopathy, or AGAINST homeopathy?
If potentized ARS ALB contains nanoparticles in quantities sufficient to produce a curative biological action, how can you say it will not initiate harmful processes also?
SEE HOW EVEN TRACES OF ARSENIC DAMAGES LIVING ORGANISM:
“Arsenic interferes with cellular longevity by allosteric inhibition of an essential metabolic enzyme pyruvate dehydrogenase (PDH) complex, which catalyzes the oxidation of pyruvate to acetyl-CoA by NAD+. With the enzyme inhibited, the energy system of the cell is disrupted resulting in a cellular apoptosis episode. Biochemically, arsenic prevents use of thiamine resulting in a clinical picture resembling thiamine deficiency. Poisoning with arsenic can raise lactate levels and lead to lactic acidosis. Low potassium levels in the cells increases the risk of experiencing a life-threatening heart rhythm problem from arsenic trioxide.[citation needed] Arsenic in cells clearly stimulates the production of hydrogen peroxide (H2O2). When the H2O2 reacts with certain metals such as iron or manganese it produces a highly reactive hydroxyl radical. Inorganic arsenic trioxide found in ground water particularly affects voltage-gated potassium channels, disrupting cellular electrolytic function resulting in neurological disturbances, cardiovascular episodes such as prolonged QT interval, neutropenia, high blood pressure, central nervous system dysfunction, anemia, and death.
Arsenic exposure plays a key role in the pathogenesis of vascular endothelial dysfunction as it inactivates endothelial nitric oxide synthase, leading to reduction in the generation and bioavailability of nitric oxide. In addition, the chronic arsenic exposure induces high oxidative stress, which may affect the structure and function of cardiovascular system. Further, the arsenic exposure has been noted to induce atherosclerosis by increasing the platelet aggregation and reducing fibrinolysis. Moreover, arsenic exposure may cause arrhythmia by increasing the QT interval and accelerating the cellular calcium overload. The chronic exposure to arsenic upregulates the expression of tumor necrosis factor-α, interleukin-1, vascular cell adhesion molecule and vascular endothelial growth factor to induce cardiovascular pathogenesis.
Tissue culture studies have shown that arsenic compounds block both IKr and Iks channels and, at the same time, activates IK-ATP channels. Arsenic compounds also disrupt ATP production through several mechanisms. At the level of the citric acid cycle, arsenic inhibits pyruvate dehydrogenase and by competing with phosphate it uncouples oxidative phosphorylation, thus inhibiting energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is also increased, which might form reactive oxygen species and oxidative stress. These metabolic interferences lead to death from multi-system organ failure, probably from necrotic cell death, not apoptosis.”
I mean to say potencies above 12c will not contain any particles of original substance. I mean to say, active principles of drugs potentized above avogadro limit are ‘molecular imprints’, which act as artificial binding sites for pathogenic molecules. Molecular Imprints cannot interfere in the interactions between biological molecules and their natural ligands, and hence they cannot produce any harmful effect in our body. Homeopathic drugs above 12c are hundred percent safe, if potentization is genuinely done.
Dear homeopaths, are you aware, by arguing that you have ‘proved’ that potentized drugs contain nanoparticles of starting materials, you are actually framing a case against homeopathy, since it raises the serious questions of nanotoxicity?
If potentized ars alb contains nanoparticles of arsenic, potentized plumbum met contains nanoparticles of lead, or potentized uranium and radium contains nanoparticles of uranium and radium, it becomes a defenseless case against homeopathy, which will obviously prompt law makers to initiate stringent regulations.
Do you remember, we were so far vouching about the ‘safety’ of potentized drugs, arguing that they do not contain even a single particle of starting material?
I mean to say ‘nanoparticle theory’ is wrong. I mean to say ‘nanoparticle theory’ is harmful for homeopathy. It will give new weapons to the enemies to attack homeopathy.
REDEFINING HOMEOPATHY 