Homeopathy and Genetic???????

You all are well qualified homeopaths and i respect your thought. I know one thing that homeopathy able to change the life and the way of thinking whether its depend on genes or not.I think Vital force is not a combination of two word, it bears whole philosophy and scientific theories and law of the natures, i thinks that Hahnemann sir was try to defined the process of human mechanism in his time without any well designed instruments and with the persons whose didn't know anything about the inner structure of body, At the time of Hahnemann sir there are no well developed branches of science, how can we say that he was not talking on the genetics.

What will you do if any person who is illiterate and don't know how the body works. Maybe you try with your best weapons to explain the idea and working process of body and you said that its a Vital force which is SPIRITUAL(Not Spiritual at all) Dynamic power of the body which governs our whole body function in the state of harmony. Like God governs us.

Assume that you have time machine and you go back to the time of Hahnemann or more year back and then ask the persons of that time "Did you know what is the RBC, WBC, and many other terms of todays science" I bet that you will listen some moaning of the peoples of that time that you are mad and have some devil spirit. Then you
realize that you have wrong approach to explain the terms of homeopathy and you said that God governs are life and he created a force which is vital (can't see it any more and not feel it) in nature. which is spiritual and dynamic and automatic and autocratic force. Then the peoples say that yes you are right.
So tell me how can Hahnemann was wrong in the explanation of idea of mechanism of body. He was used some simple terminology for this.

I think he was actually described the process of gene recombination, replication, transcription. And we are waiting from 200 year to someone come and dig the human body and try to explain us about the process of gene working.
Sorry for all this but this is my thinking that Hahnemann want to explain us about the genetic but unfortunately he was born in that era where no technology for this stuffs.

We said that we are governed by vital force till death and its not present in the dead bodies. Because without vital force all the things in world is martilistic. But what is matrialism.
Take a glass whcih is material in the formation, threw it on the floo, what will happen,the glass is broken, why? because there are some force working on it, which we called by many names. Another example of this, look at the dead body, which we think that its matrielistic now after the death of persons, then why its attracts the fleas and bugs and many other insects to produce and grow them on the dead body. I thinks there are something present in the dead body which is working after death(without the vital force).
So please tell me what is the vital force if its present after the death of persons.

I think that Vital force is nothing but its a combination of certain chemical process of the living and dead bodies or any other substances of the world. In the body.

When you see the delicious food there are scretion of slaiva and gastric juice produce in the stomach which makes us hungry and we get the food for fulfill our hunger.

When touch the anything hot or cold what happens, Several thermal receptors give us order to back off the hand from the hot and cold thing.

If we injured what will happen, we screems from the pain, pain is nothing but the sensation of that something worng happend with us, and it can be flow precived by pain receptors and converted into certain chemical process then we feel pain. If we not feel the pain than that's mean there are something missing in the cordination of the chemical process of body.

If we think about sex them then we will know that there are hormanal change occurs in our body and where it come from, certainly from the Hypothalamus and transfer from the nerve to glands and stimulate to production of hormones.

If we look at on the above examples then we know that the combination of receptors, nerves, tissues, cell and body.

So now what is vital force.

The vital force is the Chemical coordination of the Nereves, cells , tissues, many chemicals and their products. The perfect balance of these chemical of the body is make us in the harmonious state, without any disease. Its is dynamic because we can't see this, it is automatic and autocratic.
Now we tlk about the inner nature of cells, The gene is the minute thing present in every cells. A gene is a unit of heredity in a living organism. All living things depend on genes. Genes hold the information to build and maintain an organism's cells and pass genetic traits to offspring. A modern working definition of a gene is "a locatable region of genomic sequence, corresponding to a unit of inheritance, which is associated with regulatory regions, transcribed regions, and or other functional sequence regions ".

So its confirm that gene is the only agent to govern all the body for our higher purpose of living, and the higher purpose of living is that we produce healthy similar offsprings.

Now, we can able to say that homeopathy is work on the genetic level. Look if any person have disturbance in the coordination of the chemical substances which is commonded by the gene, and transfer from the generation to generation. We see the many cases of genetic disorders.

Genetic Disoder :

A genetic disorder is an illness caused by abnormalities in genes or chromosomes. While some diseases, such as cancer, are due in part to genetic disorders, they can also be caused by environmental factors. Most disorders are quite rare and affect one person in every several thousands or millions. Some types of recessive gene disorders confer an advantage in the heterozygous state in certain environments.[1]

1 Single gene disorder
1.1 Autosomal dominant
1.2 Autosomal recessive
1.3 X-linked dominant
1.4 X-linked recessive
1.5 Y-linked
1.6 Mitochondrial
2 Multifactorial and polygenic (complex) disorders.

Single gene disorder

Prevalence of some single gene disorders[citation needed]
Disorder Prevalence (approximate)
Autosomal dominant
Familial hypercholesterolemia 1 in 500
Polycystic kidney disease 1 in 1250
Hereditary spherocytosis 1 in 5,000
Marfan syndrome 1 in 4,000 [2]
Huntington disease 1 in 15,000 [3]
Autosomal recessive
Sickle cell anemia 1 in 625
(African Americans)
Cystic fibrosis 1 in 2,000
(Caucasians)
Tay-Sachs disease 1 in 3,000
(American Jews)
Phenylketonuria 1 in 12,000
Mucopolysaccharidoses 1 in 25,000
Glycogen storage diseases 1 in 50,000
Galactosemia 1 in 57,000
X-linked
Duchenne muscular dystrophy 1 in 7,000
Hemophilia 1 in 10,000
Values are for liveborn infants


A single gene disorder is the result of a single mutated gene. There are estimated to be over 4000 human diseases caused by single gene defects. Single gene disorders can be passed on to subsequent generations in several ways. Genomic imprinting and uniparental disomy, however, may affect inheritance patterns. The divisions between recessive and dominant types are not "hard and fast" although the divisions between autosomal and X-linked types are (since the latter types are distinguished purely based on the chromosomal location of the gene). For example, achondroplasia is typically considered a dominant disorder, but children with two genes for achondroplasia have a severe skeletal disorder that achondroplasics could be viewed as carriers of. Sickle-cell anemia is also considered a recessive condition, but heterozygous carriers have increased immunity to malaria in early childhood, which could be described as a related dominant condition.[citation needed] When a couple where one partner or both are sufferers or carriers of a single gene disorder and wish to have a child they can do so through IVF whichs means they can then have PDG (Pre-Implantation Genetic Diagnosis) to check whether the fertilised egg has had the genetic disorder passed on.[4]

Autosomal dominant
Main article: Autosomal dominant#Autosomal dominant gene
Only one mutated copy of the gene will be necessary for a person to be affected by an autosomal dominant disorder. Each affected person usually has one affected parent. There is a 50% chance that a child will inherit the mutated gene. Conditions that are autosomal dominant often have low penetrance, which means that although only one mutated copy is needed, a relatively small proportion of those who inherit that mutation go on to develop the disease. Examples of this type of disorder are Huntington's disease, Neurofibromatosis 1, Marfan Syndrome, Hereditary nonpolyposis colorectal cancer, and Hereditary multiple exostoses, which is a highly penetrant autosomal dominant disorder. Birth defects are also called congenital anomalies.

Autosomal recessive
Main article: Autosomal dominant#Autosomal recessive allele
Two copies of the gene must be mutated for a person to be affected by an autosomal recessive disorder. An affected person usually has unaffected parents who each carry a single copy of the mutated gene (and are referred to as carriers). Two unaffected people who each carry one copy of the mutated gene have a 25% chance with each pregnancy of having a child affected by the disorder. Examples of this type of disorder are cystic fibrosis, sickle-cell disease (also partial sickle-cell disease), Tay-Sachs disease, Niemann-Pick disease, spinal muscular atrophy, Roberts Syndrome, and Dry (otherwise known as "rice-brand") earwax.[5]

X-linked recessive
Main article: X-linked recessive
X-linked recessive conditions are also caused by mutations in genes on the X chromosome. Males are more frequently affected than females, and the chance of passing on the disorder differs between men and women. The sons of a man with an X-linked recessive disorder will not be affected, and his daughters will carry one copy of the mutated gene. A woman who is a carrier of an X-linked recessive disorder (XRXr) has a 50% chance of having sons who are affected and a 50% chance of having daughters who carry one copy of the mutated gene and are therefore carriers. X-linked recessive conditions include the serious diseases Hemophilia A, Duchenne muscular dystrophy, and Lesch-Nyhan syndrome as well as common and less serious conditions such as male pattern baldness and red-green color blindness. X-linked recessive conditions can sometimes manifest in females due to skewed X-inactivation or monosomy X (Turner syndrome).

Y-linked
Main article: Y linkage
Y-linked disorders are caused by mutations on the Y chromosome. Because males inherit a Y chromosome from their fathers, every son of an affected father will be affected. Because females inherit an X chromosome from their fathers, female offspring of affected fathers are never affected.
Since the Y chromosome is relatively small and contains very few genes, there are relatively few Y-linked disorders.[citation needed] Often the symptoms include infertility, which may be circumvented with the help of some fertility treatments. Examples are Male Infertility and hypertrichosis pinnae.[citation needed]

Mitochondrial
Main article: Mitochondrial disease
This type of inheritance, also known as maternal inheritance, applies to genes in mitochondrial DNA. Because only egg cells contribute mitochondria to the developing embryo, only mothers can pass on mitochondrial conditions to their children. An example of this type of disorder is Leber's Hereditary Optic Neuropathy.

Multifactorial and polygenic (complex) disorders

Genetic disorders may also be complex, multifactorial or polygenic, this means that they are likely associated with the effects of multiple genes in combination with lifestyle and environmental factors. Multifactoral disorders include heart disease and diabetes. Although complex disorders often cluster in families, they do not have a clear-cut pattern of inheritance. This makes it difficult to determine a person’s risk of inheriting or passing on these disorders. Complex disorders are also difficult to study and treat because the specific factors that cause most of these disorders have not yet been identified.
On a pedigree, polygenic diseases do tend to “run in families”, but the inheritance does not fit simple patterns as with Mendelian diseases. But this does not mean that the genes cannot eventually be located and studied. There is also a strong environmental component to many of them (e.g., blood pressure).
asthma
autism
autoimmune diseases such as multiple sclerosis
cancers
ciliopathies
cleft palate
diabetes
heart disease
hypertension
inflammatory bowel disease
mental retardation
mood disorder
obesity
refractive error


Ok How many above disese we homeopath cure and stop them from spreading from another generation.
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