How should muscular dystrophy be treated?

Methods of muscular dystrophy: 1. Drugs, adenosine triphosphate injection, oral vitamin E**, can temporarily increase muscle strength and relieve symptoms; 2. Appropriate physical exercise, do the best exercise, slow down the rate of muscle atrophy; 3. Massage, acupuncture, physiotherapy and other methods**Muscular dystrophy; 4. Increase the intake of high-quality protein in the diet. Muscular dystrophy is generally not easy to cure, muscular dystrophy is a progressive aggravation of limb weakness, and the degeneration of muscles that dominate the movement is characterized by hereditary diseases, is not possible, can be taken, drugs, nutritional support, to maintain the function of the heart and lungs, effectively prolong the life of the patient, can be carried out through functional exercises, and with acupuncture, physiotherapy, massage, hot compresses, etc., to prevent the aggravation of muscle atrophy, as well as joint contracture.

Patients with muscular dystrophy usually need to stay in bed, try to avoid strenuous exercise, and do some activities suitable for themselves, such as walking, jogging, and some simple activities of the limbs, which can be combined with turning over, patting the back, and expectoration to prevent complications.

Muscular dystrophy is incurable.

Muscular dystrophy is a hereditary disease, which is often manifested by weakness of the limbs due to progressive exacerbation of the disease, degeneration of the muscles that govern the movement, and the inability to **. However, symptoms can be relieved and serious complications can be prevented with aggressive**. It is recommended that patients receive nutritional support**, drugs**, and **** to maintain cardiopulmonary function and effectively prolong the life of patients.

Physiotherapy, acupuncture, warm compresses and massage are used to prevent joint contractures and further muscle atrophy.

In addition, patients should go outdoors more often, and appropriately carry out physical education exercises to enhance their own resistance. But to avoid exercising too vigorously, you can choose jogging, walking, and other ways to exercise.

Muscular dystrophy is a hereditary, genetically mutated disease that causes spinal muscular muscle atrophy and spinal muscle weakness due to the inability to synthesize proteins in the muscle membranes or inside the muscles. Because it is a hereditary disease, and it is currently known where its gene mutation site is, but like most other genetic diseases, there is no corresponding method, and there is no good symptomatic method, so muscular dystrophy cannot be **. Of course, whether it will affect his lifespan and his muscle function depends on the scope of his lesions, some muscle grinding is very limited to the scope of malnutrition, such as only limited to one limb or only limited to the face, or even limited to the eyelids, this can maintain basic life functions, the life span may not be too short, but this systemic can cause weakness, paralysis, atrophy of the limbs and muscles, respiratory muscle paralysis, and the patient dies at a very young age because of repeated pneumonia and repeated suffocation.

There is no good way to do it at the moment, and I hope you must know about it.

**Policy. : Muscular dystrophy is non-specific**, only symptomatic and supportive**, such as increased nutrition, normal activities. Physical and orthopedic forms prevent and improve spinal deformities and joint contractures, and are important for maintaining motor function.

Drug**: 1. Coenzyme Q10 Coenzyme Q10 is a fat-soluble antioxidant, which can activate the nutrition of human cells and cellular energy, and has the functions of improving human immunity, enhancing antioxidants, delaying aging and enhancing human vitality.

2. Vitamin E Vitamin E is an essential nutrient that belongs to antioxidants, which can protect nerves and muscles from oxygen free radical damage and maintain the normal development and function of nerves and muscles.

3. Other symptomatic drugs can be used, such as anti-epileptic drugs can reduce muscle spasms, immunosuppressive drugs can inhibit the human immune system to delay the destruction of muscle cells, creatine can provide energy for muscles and improve muscle strength.

The average age of death of pseudohypertrophy was 17-19 years, and the causes of death were: respiratory failure accounted for; Heart failure accounts for; Cardiopulmonary insufficiency accounts for traditional Chinese medicine that the kidney is the innate foundation, the main essence of the essence, the main bone and the marrow. Muscular dystrophy is a genetic disease, and it is also a syndrome of impotence in traditional Chinese medicine, which is most closely related to the kidneys.

At the same time, the spleen and stomach are the foundation of the day after tomorrow, metamorphosis generates qi and blood, nourishes the five internal organs, muscles, muscles and bones, and the spleen is the main muscle, the spleen and stomach are weak, the qi and blood biochemistry is insufficient, and the muscles are not nourished.

Progressive muscular dystrophy is a very harmful congenital disease, its condition is very complex, will seriously affect the normal life of patients, and even pose a threat to life safety. Therefore, after discovering the disease, we must not be negligent, and should standardize the system as soon as possible to minimize the impact of the disease on the body.

Progressive muscular dystrophy is caused by genetic defects, the current level of medical care can not be completely ** disease, after the disease develops to an advanced stage, most patients will have limb disability, and due to the atrophy of smooth muscle of the respiratory tract, it will also cause respiratory failure, which will seriously endanger the life safety of patients. But we should not be too frustrated and discouraged, after finding out that the child has this disease, we should carry out the standard system as soon as possible to delay the progression of the disease and reduce the child's symptoms. At the same time, we also need to take care of the child to prolong the child's life cycle and improve the child's quality of life.

There is no special approach to progressive muscular dystrophy, and we focus mainly on symptomatic and supportive. After discovering that the child has this condition, we should strengthen the child's nutrition and give the child more high-protein and high-calorie foods. At the same time, we can use a small dose of corticosteroids as a supplement**, which can reduce creatine phosphokinase levels, which can help to alleviate the condition.

We also need to standardize the training of children to maintain the child's muscle function as much as possible and delay the rate of muscle atrophy. If your child's respiratory muscles are affected, precautions should be taken to avoid respiratory infections.

In short, progressive muscular dystrophy can not be completely developed, and the current medical level has not overcome this problem, but parents should not be too depressed and discouraged after finding out that their children have this disease, and should actively carry out ** to delay the progression of the disease as much as possible. In the process, we must strictly follow the doctor's instructions, and also standardize the training to maintain muscle function as much as possible and improve the quality of life of children.