There are more than 600 muscles in a person's body. These muscles are helpful in providing structure and form. Along with this, it also helps in the movement of the body, so that the essential functions of a person like walking, jumping, running and breathing are completed. These muscles are divided into three forms in different parts of the body. The first is the skeletal muscles which are found in the bones of the body. These muscles are called voluntary muscles, which a person can contract and stretch at will. The second is the heart muscle which is found only in the heart and automatically contracts and expands and the rest of the muscles are present in the form of involuntary muscles in some organs like blood vessels, intestine, and uterus which expands and compressed automatically against the will of the person. All these three types of muscles are made up of cells, also known as fibers. All the muscles together perform essential functions according to the needs of the body and thus provide speed to various body movements.
When due to some reason these muscles of the body start weakening and it starts getting damaged partially or permanently, then this condition is called muscular dystrophy. In general, a muscular dystrophy is a group of diseases related to muscles that make them weak and less flexible. The group of this type of disease includes about 80 types of diseases. In some people, the disease begins in childhood, when the most common symptoms begin. In some people, its symptoms can be severe and life-threatening, and some can live for many years with mild symptoms.
Jain’s cow urine therapy clinic aims for a happy and healthy life by integrating ancient Ayurvedic knowledge with modern technology. Our therapy means cow urine including Ayurveda works on a person’s three doshas that are- The Vata, Pitta, and Kapha. These tri-energies maintain our health, any imbalance in these doshas, is responsible for human’s health and disease. We are glad to say that we have seen so many positive results through our treatment. Thousands of people got rid of many diseases after taking our treatment.
Our patients not only put an end to their disease but also live a disease-free healthy life forever. This is the reason why people are getting attention towards our therapy. Our years of research in Ayurvedic treatments have helped us advance our methodology. We aim to reach as many people as we can to build a healthy and happy society all over the world.
Some herbs function to rejuvenate body defects (Vata, Pitta, and Cough) which cause Muscular Dystrophy if they are disproportionate, according to the cow urine therapeutic approach. There are many helpful ingredients in certain Ayurvedic medicines to treat them. It increases the body's metabolism.
We use gojala in our cow-urine therapy, basically it means cow-urine extract, the main component in our medicine. This extract is made of the urine of the indigenous breeds of cow. Gojala has its own benefits because it’s beyond the possibility of any kind of contamination. It has high quality and is abundant. When gojala mixed with ayurvedic herbs it becomes more effective to treat any disease and favourable to the consequence of the particular disease. This extract is superimly tested and that’s why it’s more trustable and beneficial as well.
Therapy of cow urine gives good health and maintains balance. Today, because of our treatment, people are constantly improving their health. It improves the quality of their daily life. Ayurvedic medicine and cow urine can be used as a complementary therapy to minimize various side effects caused by the use of heavy doses, mental stress, radiation, and chemotherapy. We teach people how to live a happy, stress-free life with incurable diseases. Thousands of people are living a balanced life after receiving our treatment. This is a great achievement for us to bring them the life of their dreams.
Cow urine has a special place in Ayurveda, which is also considered beneficial for diseases like muscular dystrophy. Our years of hard work show that almost many complications of muscular dystrophy disappear with the use of Ayurvedic herbs. There is a great relief which our patients feel problems with balance, difficulty in standing without support, muscle pain and stiffness, flexion of the spine, difficulty in walking, difficulty in breathing, joint pain, swelling in the leg muscles in tremors, shin splints, frequent falls, difficulty in getting up from a lying or sitting position, learning disabilities, delayed growth, muscle cramps, walking on toes, etc. The treatment improves the patient's immune system which works optimally for problems related to other complications of muscular dystrophy.
Cow urine remedy is itself a great deal of optimism if we are speaking about life expectancy. Any disorder both small or in a crucial stage comes with a bad influence on a human’s physique and exists for a variety of years, now and again for a lifetime. Once the disorder is recognized, life expectancy is brief however now not with cow-urine therapy. Our historical remedy now not solely treats the disorder however additionally will increase the lifespan of that individual without leaving any toxins in his physique and this is our last aim.
“Sarve bhavantu sukhinah, Sarve santu niramayah, Sarve bhadrani pashyantu, Maa kaschit dukha bhag bhavet" means let all be joyful, let all be free of sickness, let all see the reality, let no one suffer." We want our culture to be like this by adopting this saying. Our therapy accomplishes this by providing efficient care, enhancing the life expectancy of affected patients, and reducing drug dependency. In this new age, our treatment has more benefits and fewer risks than any medicinal solutions available. There are more benefits and nil risks to our therapy.
In comparison to a wide range of medical practices, we focus on the root cause of the disease and the factors that may increase the chance of disease recurrence, not just the management of the disease. By using this method, we have successfully reduced the recurrence rate and pointed out a new direction for people's lives so that people can live better emotionally and physically.
Some factors and risk factors may be responsible for developing muscular dystrophy, which includes -
To keep the body muscles healthy and prevent them from getting damaged, many genes make proteins that protect muscle fibers, strengthen muscles and protect them from injury. But whenever there is a problem in one of these genes, it starts making the wrong protein, the wrong amount, or damaged protein, which leads to the problem of muscular dystrophy.
Genetic mutations inherited from parents are the specific cause of each form of muscular dystrophy. It is caused by the presence of abnormal genes that interfere with the way of proteins in the body that develop muscle. Abnormal genes (mutations) interfere with the production of proteins needed to build healthy muscles and cause muscular dystrophy.
Sometimes, due to some reason, there is a defect in the egg or fetus growing in the womb of a pregnant woman, due to which the muscles of the born child become weak and they start having problems with muscular dystrophy.
Muscular dystrophy can be a disease that is passed down from one generation to the next in the family. If a family member has ever had a problem with muscular dystrophy during their lifetime, the problem may be passed on to the other member as a result of a problem in their genes.
Muscular dystrophy can occur in both sexes and all ages and ethnicities. However, the most common type, Duchenne muscular dystrophy, usually occurs in young boys. People with a family history of muscular dystrophy have a higher risk of developing the disease or passing it on to their children.
When a person has a low body weight as measured by body mass index, they are more prone to muscular dystrophy. People with an average body mass index of 17.3 BMI, or less, are at higher risk for this type of problem.
Poor lung function, high blood pressure during breathing, poor lifestyle, the high blood concentration of proteins associated with heart damage, active genetic structure in specific chromosomes, etc. are other factors that may play a role in increasing the risk of muscular dystrophy.
Certain measures can help manage and slow down its symptoms, including -
Signs and symptoms of muscular dystrophy include -
Some of the main types of muscular dystrophy include -
It is the most common type of muscular dystrophy, which is caused by a defect in the gene that makes the dystrophin protein in the body. This protein works to strengthen the muscles in the body. Due to its deficiency, the muscles start getting damaged and the person gradually becomes weak. This type of problem mostly occurs in boys between the age of 2 to 6 years. Symptoms include frequent falls, stunted growth, difficulty lying down, running, walking, muscle aches, and stiffness. Due to Duchenne muscular dystrophy, children can sometimes suffer from heart problems.
In this type of muscular dystrophy, the symptoms appear more slowly and are relatively less dangerous. Its main symptoms are muscle weakness and breakdown, which usually do not appear until the age of 10 years. Sometimes their symptoms are not visible even till the person becomes an adult. People suffering from it have trouble with the heart, breathing, bones, muscles, and joints.
Muscle weakness usually affects the face, shoulders, hips, and lower legs. Due to this, the troubled person has trouble raising the hand, whistling, and closing their eyes tightly. It usually begins in adolescence but can develop in childhood or as early as age 50.
In this type of muscular dystrophy, the muscles of the hip and shoulder are usually affected first. Its onset usually begins in childhood or adolescence. Generally, it can occur in both men and women. It weakens the muscles of the arms, shoulders, thighs, and hips of the patient. People with this type of muscular dystrophy may have difficulty lifting the front of the leg.
It is characterized by the inability of the muscle to relax after contraction. The muscles of the face and neck are usually the first to be affected. People with this form usually have long, slender faces, drooping eyelids, and swan-like necks. It is more troublesome in adolescents. This includes muscle weakness and eye and heart problems. The person also feels difficulty in swallowing.
This is also a type of muscular dystrophy and mostly affects boys. These are a group of rare, inherited muscle diseases (myopathies). EDMD causes weakness in the baby's shoulders, upper arms, and thighs. Symptoms usually appear in late childhood, early adolescence, or puberty.
A person suffering from the problem of muscular dystrophy may face many complications which include -
