I do not agree with the current campaign for mass distribution of Arsenic Alb 30 as “immune booster”, being conducted by a section of homeopaths with the official support of AYUSH authorities. I have sufficient reasons for this disagreement.
Call it HOMEOPATHIC PROPHYLACTIC. It is the appropriate expression.
Post-avogadro homeopathic medicines contain molecular imprints of constituent molecules as their active principles. These molecular imprints act as ARTIFICIAL BINDING POCKETS for pathogenic molecules such as viral glycoproteins. They do not act upon our biological molecules or produce any effect unless pathological molecules having conformational affinity are present. Obviously, our medinces act ONLY if pathogenic molecules are present in our body. Molecular imprints fight viral infections by preventing from binding to our cells, not by enhancing IMMUNITY. That is why I say homeopathy medicines can prevent a viral disease only if taken continuously until epidemic is over.
COVID 19 is spreading very fast, and is almost going out of control in many states. Lives of people are in danger.
Please reconsider your earlier advice of distributing Arsenic Album 30 as preventive. It is not sufficient for mass prevention.
A disease-specific COMBINATION of all indicated homeopathic drugs in 30c potencies is essential to ensure protection on mass scale.
Dosage as well as frequency also have to be reconsidered. My suggestion is drop doses twice daily directly on tongueue until epidemic is over.
is an insult to HOMEOPATHY!
Nobody ever proved or can prove post-avogadro homeopathic medicines could induce production of immune bodies or initiate an immune process.!
Only way the molecular imprints contained in post-avogadro diluted homeopathic medicines act is to bind to the pathogenic molecules, deactivate them, and remove the pathological molecular inhibitions they produced.
In the absence of pathogenic molecules having conformational affinity, molecular imprints have no any action in the body.
Molecular imprints cannot interfere in the normal interactions between biological molecules and their natural ligands.
They cannot produce any positive or negative changes in the body. They cannot make us more healthy or more diseased, when there are no pathological molecules available for binding.
You can realize the folly involved in calling homeopathy medicines as IMMUNE BOOSTERS, only if you understand the biological mechanism by which post-avogadro drugs act.
1. Does that drug in 30c dilution actually contains the original drug ?
2. If “yes”, in what form original drug substance exists in 30c dilution? As molecules, atoms, nanoparticles, electrons, protons, subatomic particles or any other material form? Or does it exists in the form of some “dynamic energy”, “vial force”, “vibrations” or any other “immaterial form?
3. What is the biological mechanism by which the drug in 30c dilution produces immune boosting, prophylactic or therapeutic effects?
4. When answering these questions, please do not forget, 30c is a dilution of 1 in 1 and 60 zeros, much above avogadro limit. Above avogadro limit, there is no any chance for even a single particle of original substance to exist.
5. If you say Arsenic Alb 30 contains NANOPARTICLES of original drug, you will have to explain where from this unlimited supply of nanoparticles come, to be present in each and every split drop of the preparation even in such high dilutions! That will be possible only if new matter particles are generated from nothingness during the process of potentization!
6. Do you think the complex chemical molecules, chemical properties of which decide the medicinal properties of the substance, could be split into elemental atoms during potentization? Do you think the mechanical energy of shaking a few times will generate the huge energy required to break the covalent bonds that hold the atoms together in a molecule? If you think it is possible, can you split a simple water molecule into hydrogen and oxygen by SHAKING?
Dear sir, you cannot evade these important questions by simply quoting the aphorisms of the master, or abusing and ridiculing me for asking these kinds of uncomfortable questions!
1. Does Arsenic Alb 30 actually contains Arsenic Trioxide?
2. If “yes”, in what form Arsenic Trioxide exists in Arsenic Alb 30? As molecules, atoms, nanoparticles, electrons, protons, subatomic particles or any other material form? Or does it exists in the form of some “dynamic energy”, “vial force”, “vibrations” or any other “immaterial form?
3. What is the biological mechanism by which Arsenic Alb 30 produces, immune boosting, prophylactic or therapeutic please?
4. When answering these questions, please do not forget, 30c is a dilution of 1 in 1 and 60 zeros, much above avogadro limit. Above avogadro limit, there is no any chance for even a single particle of original substance to exist.
And of course another sect of them will claim it was sepia 200 two drops spray that did the work! Just like the claim going around that covid 19 is being prevented in some states by drinking cow urine!
Next generation homeopathy students will naturally be taught in colleges that it was homeopathy that defeated COVID 19 outbreak of 2020!
Some people claim they protected thousands by giving “holy ashes” brought from Himalaya! Some others claim they protected people using holy water from Ganges!
Millions are claimed to be protected by drinking cow urine! They might have consumed cow dung also!
One swamiji claims he can prevent corona by pranayama or breathing exercises!
Some people conduct pujas to prevent corona! Clapping hands and ringing bells on roads to eradicate covid were also performed all over the country!
Millions are also claimed to be protected by the mysterious vibrations emanating from homeopathic pills they distributed!
The truth is that spread of covid 19 was contained at least to this level by massive governmental vigilance, quaretines, isolations, lockdowns, social distancing, handwashing, sanitizers, masks etc! And every charlatans are claiming credits for it!
Had the whole world gone crazy by covid fear?
All the infected ones were identified in time, strictly quatentined, their root maps were published, primary and secondary contacts were identified and isolated, a massive “break the chain” campaign was implemented with active cooperation of public, lockdown was brought much before it came at national level, all of which ultimately prevented the spread of covid in the state.
Homeopaths please do not make homeopathy ridiculed and humiliated by making bogus claims!
AS with any other VIRAL DISEASE, homeopathy should be capable of preventing and curing covid-19. I have no least doubt the efficacy of homeopathy. But it should be established not by broadcasting bogus claims propagated by some irresponsible persons. That is my point.
Before raising claims, it should be proved by conducting systematic and well monitored trials, using appropriate prescriptions, appropriate medicines, appropriate potencies, appropriate doses and appropriate frequencies. You cannot prove the efficacy of homeopathy by giving some medicines “along with allopathic medicines” as some people are trying to do now.
You cannot evade from scientific questions by simply abusing the person who raises questions, and raising counter questions about his qualifications for questions. No special qualifications are necessary to question unscientific, superstitious and nonsense ideas that may harm the community. Mind it.
If you have any scientifically viable argument that “fragility and breaking of human genomes due to the disturbance of earth’s electromagnetic field” is the FUNDAMENTAL CAUSE of covid-19, prove it by scientific methods before broadcasting it to the community.
Existing scientific knowledge do not agree with your theory that “viruses do not come from outside, but from inside of individuals”.
Especially in this time global pandemic of covid-19, your arguments have a lot of dangerous implications. Need for lock downs, shutting of flights, isolation, quarantine, handwashes, social distancing, face masks, sanitization, and every preventive measures WHO and Govt have advised and globally practiced to prevent spread of COVID-19 will be irrelevant and unnecessary if your theory is right.
Please understand, you are questioning the rationale of ongoing fight against COVID 19, and you are bound to attract legal actions for violation of provisions of epidemics act currently in force.
In the current grave circumstances, you are not authorised to broadcast all your whims and fancies that may weakn the social preventive measures against COVID.
It will be very dangerous situation for the whole society around him, if someone belonging to the class of your “blind followers” dare to defy the directives of health officials, believing your words that covid is not spread from person to person, but come from his own “inside”.
Please think about the dangerous situation that may be created if people start believing your theory that covid could be cured and prevented by correcting the “vibrations” by applying some sepia 200 on his toes, and putting same medicines around the house!
Dear sir, please understand, by broadcasting this kind of dangerous ideas about corona virus infection in the current circumstances , you have actually done a big crime against humanity as a whole. Kindly withdraw your video and disown it as early as possible, as it is being widely propagated and broadcasted by your foolish followers who failed to realize it’s dangerous social and legal implications.
I know you do not like this kind of questions. And most of you will say those who ask this kind of questions are “enemies” of homeopathy. But for me, these questions arise from my love and concern for homeopathy, and from my desire to make it scientific! I know, your intolerance to scientific questions actually come from your realization that you are incapable of providing answers to them. Whether you like it or not, I will go on asking questions until I get satisfactory answers.
And remember, homeopathy will get recognized as a medical science only when you are capable of answering these questions in a way fitting to the modern scientific knowledge system!
Engaging in inappropriately designed and inaccurately conducted TRIALS based on blind beliefs and overenthusiasm about the “infallibility” of so-called “fundamental principles”, without any scientific idea regarding the active principles and biological mechanism of actions of homeopathic drugs may lead to failures of your trials. Ultimately, it will be doing big damages to the future of homeopathy.
As far as scientific people are concerned, Ars Alb 30 is nothing but a mixture of water and alcohol without any drug molecule in it. We will have to explain a lot
Some “researchers” will say they cured covid with camphor, some others with sepia, some others with Justicia, some others with zincum, some with Ars Alb, some with “multiple drugs”, and some other drug in material medica, depending upon their tastes and fancies!
Since there are no controls or blinding, this kind of trials are not going to be accepted by scientific community as valid proofs for anything.
What will remain at the end will be enough stuff for homeopaths to celebrate, and for skeptics to ridicule homeopathy!
ONE THING IS SURE. IT WILL BE GOING TO INFLICT MORE INJURIES TO THE SCIENTIFIC CREDIBILITY OF HOMEOPATHY!
You are bound to fail, if you think you can convince the skeptics regarding the efficacy of potentized homeopathic drugs by conducting conventional types of ‘clinical trials’ or RCTs as they demand for.
You can never expect ‘individual-based’ homeopathic drugs to be proved using the protocols of testing drugs in ‘disease-based’ modern medicine. Asking to ‘prove’ homeopathic drugs using protocols of allopathic drug trials is like trying to measure ‘length’ using units of ‘mass’.
Allopathic methods of ‘drug trials’ are applicable to ‘molecular forms’ of drugs only. But potentized homeopathic drugs, different from allopathic drugs, contain only ‘molecular imprints’, which can act only up on pathogenic molecules having specific conformational affinity. That means, potentized drugs can act only if indicated by similarity of symptoms.
You cannot ignore this peculiarity of homeopathy in matters of active principles as well as mechanism of drug actions while designing ‘drug trials’ for homeopathy.
In homeopathy, you cannot ‘verify’ action of a particular drug on a particular disease- you have to ‘verify’ action of ‘indicated drugs’ up on indicated individual patients, since different people with same disease may need different drugs.
Same time, disease-specific combinations of post-avogadro dilutions could be subjected to Random Controlled Trials in the same way as allopathic drugs. This is the most effective way to prove that potentized homeopathy drugs are not placebo, fraud, or “mere water”, but they really work.
As far as skeptics as well as homeopaths hesitate to accept this peculiarity of potentized homeopathic drugs and agree to design the ‘trials’ of disease-specific combinations of post-avogadro dilutions, there is no way to convince the scientists that ‘homeopathy’ works’.
I WANT TO REPEAT: WE CAN PROVE THE EFFECTIVENESS OF HOMEOPATHY THROUGH RANDOM CONTROLLED TRIALS ONLY BY USING DISEASE-SPECIFIC COMBINATIONS OF POST-AVOGADRO DILUTIONS.
Some “researchers” will say they cured covid with camphor, some others with sepia, some others with Justicia, some others with zincum, some with Ars Alb, some with “multiple drugs”, and some other drug in material medica, depending upon their tastes and fancies!
Since there are no controls or blinding, this kind of trials are not going to be accepted by scientific community as valid proofs for anything.
What will remain at the end will be enough stuff for homeopaths to celebrate, and for skeptics to ridicule homeopathy!
ONE THING IS SURE. IT WILL BE GOING TO INFLICT MORE INJURIES TO THE SCIENTIFIC CREDIBILITY OF HOMEOPATHY!
You are bound to fail, if you think you can convince the skeptics regarding the efficacy of potentized homeopathic drugs by conducting conventional types of ‘clinical trials’ or RCTs as they demand for.
You can never expect ‘individual-based’ homeopathic drugs to be proved using the protocols of testing drugs in ‘disease-based’ modern medicine. Asking to ‘prove’ homeopathic drugs using protocols of allopathic drug trials is like trying to measure ‘length’ using units of ‘mass’.
Allopathic methods of ‘drug trials’ are applicable to ‘molecular forms’ of drugs only. But potentized homeopathic drugs, different from allopathic drugs, contain only ‘molecular imprints’, which can act only up on pathogenic molecules having specific conformational affinity. That means, potentized drugs can act only if indicated by similarity of symptoms.
You cannot ignore this peculiarity of homeopathy in matters of active principles as well as mechanism of drug actions while designing ‘drug trials’ for homeopathy.
In homeopathy, you cannot ‘verify’ action of a particular drug on a particular disease- you have to ‘verify’ action of ‘indicated drugs’ up on indicated individual patients, since different people with same disease may need different drugs.
Same time, disease-specific combinations of post-avogadro dilutions could be subjected to Random Controlled Trials in the same way as allopathic drugs. This is the most effective way to prove that potentized homeopathy drugs are not placebo, fraud, or “mere water”, but they really work.
As far as skeptics as well as homeopaths hesitate to accept this peculiarity of potentized homeopathic drugs and agree to design the ‘trials’ of disease-specific combinations of post-avogadro dilutions, there is no way to convince the scientists that ‘homeopathy’ works’.
I WANT TO REPEAT: WE CAN PROVE THE EFFECTIVENESS OF HOMEOPATHY THROUGH RANDOM CONTROLLED TRIALS ONLY BY USING DISEASE-SPECIFIC COMBINATIONS OF POST-AVOGADRO DILUTIONS.
At the end, only things remaining for homeopathy will be some bogus unconvincing claims from homeopaths, and lot of ridicules from the other side!
Even a few drops of “holy water” will be enough to make a CLAIM of cure in a disease more than 80% of which is resolved without any medication at all, when you are not expected to explain HOW IT ACTS!
“Scientific Advisory Board considered that the same medicine has been advised for prevention of Influenza like illnesses. As one of the constituents of a formulation , Arsenicum Album has been shown to affect the HT-29 cells and human macrophages”. It reduced the expression of reporter gene GFP in transfect HT 29 cells, and reduced TNF-alfa release in macrophages. Moreover, Arsenic Album is a common prescription in the cases of respiratory infections in day to day practice.”
If we examine the above reasoning, it contains THREE points:
1. ” the same medicine has been advised for prevention of Influenza like illnesses”.
2. “As one of the constituents of a formulation, Arsenicum Album has been shown to affect the HT-29 cells and human macrophages”.
3. It reduced the expression of reporter gene GFP in transfect HT 29 cells, and reduced TNF-alfa release in macrophages.”
4. “Arsenic Album is a common prescription in the cases of respiratory infections in day to day practice.”
Point 1 and 4 are obviously of no relevance as a scientific reasoning, other than quoting hearsays. How could anybody recommend Ars Alb or any other medicine for Covid 19, on the simple reasons that “same medicine has been advised for prevention of Influenza like illnesses”, or “it is a common prescription in the cases of respiratory infections in day to day practice”? It is totally unscientific and illogical.
Coming to POINT 2, See on Wikipedia what is HT-29 cells: “HT-29 is a human colon cancer cell line used extensively in biological and cancer research. HT-29 cells form a tight monolayer while exhibiting similarity to enterocytes from the small intestine. HT-29 cells overproduce the p53 tumor antigen, but have a mutation in the p53 gene at position 273, resulting in a histidine replacing an arginine. The cells proliferate rapidly in media containing suramin, with corresponding high expression of the c-myc oncogene. However, c-myc is deregulated, but may have a relation with the growth factor requirements of HT-29 cells”.
Even if Arsenicum Album has been proved to act upon HT 29 cells, what is its relevance in covid 19 treatment? Has anybody proved that HT 29 cells are anyway involved in pathology of corona? Any argument or any evidence? Nothing!
Another thing is, the paper shown in the reference actually is regarding a study regarding action of MOLECULAR forms of Arsenic Trioxide on HT 29 cells. Does our ARSENIC ALB 30 contain any molecules of Arsenic Trioxide?
Coming to POINT 3, see what WIKIPEDIA says: The green fluorescent protein (GFP) is a protein composed of 238 amino acid residues (26.9 kDa) that exhibits bright green fluorescence when exposed to light in the blue to ultraviolet range. In cell and molecular biology, the GFP gene is frequently used as a reporter of expression.[5] It has been used in modified forms to make biosensors, and many animals have been created that express GFP, which demonstrates a proof of concept that a gene can be expressed throughout a given organism, in selected organs, or in cells of interest. GFP can be introduced into animals or other species through transgenic techniques, and maintained in their genome and that of their offspring. To date, GFP has been expressed in many species, including bacteria, yeasts, fungi, fish and mammals, including in human cells”.
How the “reduced the expression of reporter gene GFP in transfect HT 29 cells” by the action of MOLECULAR forms of Arsenic Trioxide becomes relevant in the treatment of covid 19?
Regarding the reference to “reduced TNF-alfa release in macrophages” by the action of molecular forms of Arsenic Trioxide, somebody has to explain how it justifies the use of ARS ALB 30 in covid 19. It is well known that TNF alfa plays a role in induction of inflammations and antiviral responses. But it is Arsenic Trioxide in MOLECULAR FORM. Our Arsenic alb 30 is a 1/1and 60 zeros dilution of Arsenic Trioxide. Can anybody say Arsenic Trioxide molecules will be retained in a dilution 3 times above Avogadro limit? If not, in what form Arsenic Trioxide will be available in Ars Alb 30, and what will be the biological mechanism by which it acts? Without getting answers to this question, do you expect scientific community to recognize homeopathy as a medical system?
You can never expect ‘individual-based’ homeopathic drugs to be proved using the protocols of testing drugs in ‘disease-based’ modern medicine. Asking to ‘prove’ homeopathic drugs using protocols of allopathic drug trials is like trying to measure ‘length’ using units of ‘mass’.
Allopathic methods of ‘drug trials’ are applicable to ‘molecular forms’ of drugs only. But potentized homeopathic drugs, different from allopathic drugs, contain only ‘molecular imprints’, which can act only up on pathogenic molecules having specific conformational affinity. That means, potentized drugs can act only if indicated by similarity of symptoms.
You cannot ignore this peculiarity of homeopathy in matters of active principles as well as mechanism of drug actions while designing ‘drug trials’ for homeopathy.
In homeopathy, you cannot ‘verify’ action of a particular drug on a particular disease- you have to ‘verify’ action of ‘indicated drugs’ up on indicated individual patients, since different people with same disease may need different drugs.
Same time, disease-specific combinations of post-avogadro dilutions could be subjected to Random Controlled Trials in the same way as allopathic drugs. This is the most effective way to prove that potentized homeopathy drugs are not placebo, fraud, or “mere water”, but they really work.
As far as skeptics as well as homeopaths hesitate to accept this peculiarity of potentized homeopathic drugs and agree to design the ‘trials’ of disease-specific combinations of post-avogadro dilutions, there is no way to convince the scientists that ‘homeopathy’ works’.
I WANT TO REPEAT: WE CAN PROVE THE EFFECTIVENESS OF HOMEOPATHY THROUGH RANDOM CONTROLLED TRIALS ONLY BY USING DISEASE-SPECIFIC COMBINATIONS OF POST-AVOGADRO DILUTIONS.
MIT view is that it is effective as palliatives to use ‘disease-specific’ combinations of ‘molecular imprinted’ forms (potencies above Avogadro limit- 12c and onwards) of two or more homeopathic drugs selected on the basis of common symptoms and biochemical evaluations of specific diseases. But such ‘disease-specific’ combinations will not offer ‘total cure’ for patients, without incorporating drugs selected on the basis of symptoms also. This approach also is very close to the method of ‘banerji protocols’ that makes ‘specific’ prescriptions based on ‘disease diagnosis’ as well as symptomatology..
I am talking on the basis of my concepts of ‘molecular imprinting’ involved in potentization. I perceive all crude drugs as combinations of diverse types of constituent drug molecules. I perceive even the so called potentized ‘single’ drug as combinations of diverse types of individual drug molecules contained in the drug substance used for potentization.
My stand on this issue is based on my understanding of diseases as multitudes of pathological derangement in the organism, caused by diverse of types of molecular inhibitions caused by different types of pathogenic agents, and therapeutics involves the removal of those inhibitions using appropriate molecular imprints.
I am talking on the basis of my understanding of ‘similia similibus curentur’ as: “pathological molecular inhibitions caused by specific pathogenic molecules and expressed through a certain group of subjective and objective symptoms, could be removed by applying ‘molecular imprints’ of drug molecules that could create similar molecular inhibitions and symptoms in a healthy organism when applied in crude form.
That makes the difference between my views and classical homeopathy. I know, homeopaths trained and experienced in classical homeopathy cannot agree with my views on this topic.
MIT or Molecular Imprints Therapeutics refers to a scientific hypothesis that proposes a rational model for biological mechanism of homeopathic therapeutics.
According to MIT hypothesis, potentization involves a process of ‘molecular imprinting’, where in the conformational details of individual drug molecules are ‘imprinted’ or engraved as hydrogen-bonded three dimensional nano-cavities into a supra-molecular matrix of water and ethyl alcohol, through a process of molecular level ‘host-guest’ interactions. These ‘molecular imprints’ or ‘hydrosomes’ are the active principles of post-avogadro dilutions used as homeopathic drugs.
Due to ‘conformational affinity’, molecular imprints can act as ‘artificial key holes’ or ‘ligand binds’ for the specific drug molecules used for imprinting, and for all pathogenic molecules having functional groups ‘similar’ to those drug molecules. When used as therapeutic agents, molecular imprints selectively bind to the pathogenic molecules having conformational affinity and deactivate them, thereby relieving the biological molecules from the inhibitions or blocks caused by pathogenic molecules. According to MIT hypothesis, this is the biological mechanism of high dilution therapeutics involved in homeopathic cure.
According to MIT hypothesis, ‘Similia Similibus Curentur’ means, diseases expressed through a particular group of symptoms could be cured by ‘molecular imprints’ forms of drug substances, which in ‘molecular’ or crude forms could produce ‘similar’ groups of symptoms in healthy individuals. ‘Similarity’ of drug symptoms and diseaes indicates ‘similarity’ of pathological molecular inhibitions caused by drug molecules and pathogenic molecules, which in turn indicates conformational ‘similarity’ of functional groups of drug molecules and pathogenic molecules. Since molecular imprints of ‘similar’ molecules can bind to ‘similar’ ligand molecules by conformational affinity, they can act as therapeutic agents when applied as indicated by ‘similarity of symptoms’.
No body in the whole history could so far propose a hypothesis about homeopathy as scientific, rational and perfect as MIT, explaining the molecular process involed in potentization, and the biological mechanism involved in ‘similia similibus curentur’, in a way fitting well to modern scientific knowledge system.
Arsenic Album or Arsenic Trioxide is a chemical substance that can inhibit more than 200 essential enzymes in our body involved in diverse types of biomolecular processes related with genetic transcription, metabolism, energy conversions etc etc. This is due to the ability of Arsenic ions to bind to the cysteine radicals which are part of active sites all enzymes. Almost every biochemical pathways in the living body are deranged by the action of arsenic. This is the reason why the homeopathic materia medica of arsenic album is so rich with symptoms associated with almost all organs and systems of the body.
It is an already established fact that during viral infections, persons having high levels of arsenic in their body are prone to develop serious complications such as respiratory failure, acute myocardial degeneration, renal failures, liver failures, multiple organ failures etc faster than those having low arsenic levels. My suggestion to the experts involved in covid 19 research is that determination of arsenic levels in the body of covid patients should be made mandatory, so that high risk people could be identified and better care provided.
Arsenic content may be high in people due to living in certain areas, consuming arsenic rich ground water, cigarette smoking, eating unpolished rice, prawns and crabs, exposure to arsenic containing environments, etc etc. Arsenic may enter the body through contaminated liquors, Chinese, Ayurvedic, unani or Herbal preparations, industrial exposures, chemically treated wooden furniture etc also. Arsenic content will naturally be high in aged people, as it has a tendency to accumulated in the body over years through exposures.
Researchers working upon arsenic toxicity problems in certain arsenic affected countries have already proved that ARSENIC ALBUM 30 can antidote and reverse the chronic effects of arsenic toxicity, and remove the symptoms.
Arsenic Album 30 contains MOLECULAR IMPRINTS of arsenic trioxide molecules. Molecular imprints are three dimensional nanocavities formed in water-alcohol supra-molecular matrix through a host-guest interactions between templates and diluent medium during the process of homeopathic POTENTIZATION. Molecular imprints of arsenic trioxide contained in Arsenicum Album 30 can act as artificial binding pockets for arsenic ions and deactivate them, thereby removing the molecular inhibitions they have produced in the enzyme systems of the body.
By using Arsenicum Album 30 in sufficient quantities and frequencies to provide molecular imprints in optimum levels, it will be possible to prevent dangerous complications and multiple organ failures in covid 19 patients, so as to prevent the chances of morbidities due to the disease. Covid 19 deaths could prevented by use of Arsenic Alb 30.
I don’t know how to get this vey important message reach the right persons in right time, or how to convince the scientific basis of this approach described above.
A word to homeopaths : Homeopaths currently involved in distribution of Arsenicum Album 30 should realize the hard truth that the dosage you are giving now is actually of no use. 4 or 5 medicated sugar pills you give now cannot provide the sufficient quantity of molecular imprints required to produce desired biological effects. To ensure optimum protection, medicine should be used in drop doses at least twice a day until the epidemic threat is over.
Please understand, it is not any mysterious “dynamic energy” or “vibrations” that work in our potentized drugs. It is MOLECULAR IMPRINTS, that act as “artificial binding pockets” for pathogenic molecules, and deactivate them.
I am not sure whether Arsenic album 30 will prevent or not covid. Be sure it will surely prevent complications even if you get infected. But dosage should be reconsidered. I would suggest minimum 1 or 2 drops direct on tongue bds until epidemic is over.
REDEFINING HOMEOPATHY 