"The human body is composed of billions of cells, which are the fundamental units of life. These cells are too small to be seen with the naked eye, but each one has a specific function that contributes to the overall health and functioning of the body. In fact, without cells, the body would be unable to perform any of its vital functions.
Within each cell, there is a nucleus that contains DNA (deoxyribonucleic acid) and RNA (ribonucleic acid). DNA is made up of genes, which are the carriers of genetic properties and are found in chromosomes. There are approximately 36,000 genes in a cell. When a child is born, they inherit 22 chromosomes from their mother and 22 chromosomes from their father, which are the same, known as autosomes. The 23rd pair of chromosomes determines the sex of the individual, either XX (female) or XY (male).
The DNA in a person's body contains all the genetic information necessary for their development and function. It is like a pen drive that stores all the body's information. This genetic information is passed from one generation to the next through DNA. The entire program of the body is contained within the DNA, determining characteristics such as:
- Hair color
- Eye color
- Liver function
- Sex
- Height
- Skin color
- Facial features
- Body shape
- Intelligence
- Susceptibility to certain diseases
The information from the DNA is transmitted to the cytoplasm, then to the RNA, and finally, all the information is expressed, and the body follows it. This complex process highlights the importance of genetic disorders and the role of homeopathy in treating them.
Homeopathy is a system of medicine that targets the root cause of a disease, which is often related to genetic predispositions. By understanding the genetic makeup of an individual, homeopaths can tailor their treatment to address specific genetic disorders and promote overall health and well-being."
"DNA corrupt”
Human body has cells and nucleus is present in the cell. Nucleus contains DNA, which is the carrier of genetic properties, carrying genetic information from one generation to the next. There are approximately 30,000 genes in the human genome, arranged on 46 chromosomes. How does DNA get damaged?
1. We inherit damaged DNA from birth. When a child is in the mother's womb, any problems with the DNA of either parent can be passed on to the child.
2. When a person contracts a disease like Tuberculosis, Cancer, Typhoid, Malaria, Helicobacter pylori, E. coli, Streptococcus, etc., due to viruses, bacteria, fungi, or parasites, it can damage DNA over time. The disease first affects tissues, then destroys the mucous membrane, and eventually reaches the bloodstream, where it can stay for 6 months to 1 year before reaching organs through the blood. It can then remain dormant for 5-7 years, damaging the nucleus wall outside the cytoplasm nucleus of the cell. This damage can lead to genetic disorders, which can be passed down from one generation to the next. It damages the cell wall just like a soldier breaks a fort in a war. The king (DNA) remains safe inside the fort (nucleus) because there is a strong wall structure around the nucleus, protecting the DNA. Slowly, over 25-30 years, the virus or bacteria breaks the cell wall and reaches the DNA, damaging the programming of our body stored in the DNA.
Are there any diseases passed from one generation to another, from parents to children? Yes, genetic diseases. For example, if someone has a family history of muscular dystrophy, it can be passed on to the next generation. Similarly, conditions like high blood pressure, diabetes, cancer, typhoid, and tuberculosis can also be inherited by children from their parents."
Examples of genetic disorders include muscular dystrophy, high blood pressure, diabetes, cancer, and tuberculosis. These conditions can be inherited by children from their parents, making them more susceptible to developing these diseases.