How should muscle nutrition be treated, and what should I do if muscle nutrition is not good How to

It is recommended to use traditional Chinese medicine**.

Muscular dystrophy is very good in daily life people still do not understand this disease, you must know that if the disease is serious, it will seriously endanger the life of the patient, so it can effectively understand the symptoms of the disease, can be carried out in time, and can reduce the pain of the patient to a certain extent. Patients also need to adjust their hearts to a certain extent when they are in **.

Many people do not know about muscular dystrophy, in fact, malnutrition is also known as progressive muscular dystrophy. And depending on the constitution of the non-accolades of the same person, there will be different degrees of symptoms. If you understand the symptoms and are able to do it correctly according to the symptoms, you can greatly reduce the patient's suffering.

Symptoms that occur after the onset of the disease are divided into five types, including pseudohypertrophic, limb-girdle, scapulohumeral, ophthalmo, and distal. In early childhood, the main manifestations of the disease are slow walking, easy to fall, and it will also delay the age of the child's walking, and if the patient has lung infection and pressure ulcers, the patient will die before the age of 20 in most cases. This is called false hypertrophy.

Scapulohumeral symptoms are characterized by the inability to completely close the eyes during sleep; Symptoms of the limb-girdle type are weakness of the pelvic girdle muscles and pseudo-locking.

1: After the occurrence of muscular dystrophy, it is mainly based on drugs, and the drugs used in medicine for this disease mainly include microbiotic E, dexamethasone, glucose, insulin and other drugs, which can well supplement the lack of vitamins or nutrition for patients.

2: If the symptoms are severe, it can also be performed by surgery**, and the main methods in medicine at present require myoblast transplantation or bone marrow stem cell transplantation.

3: At the time, it can also be assisted by traditional Chinese medicine, which can effectively improve the patient's condition and heal more quickly.

4: Acupuncture of traditional Chinese medicine can also be used to alleviate the patient's symptoms, and it can be effective**The patient's condition.

5: And in the daily life, you can carry out appropriate exercises, so that the patient's joints have sufficient activity, which can effectively delay the occurrence of muscle atrophy.

According to the above situation, we can effectively understand the symptoms of muscular dystrophy, and after understanding, we can effectively prevent and alleviate the patient's condition, which can effectively reduce the incidence of the patient. Patients should pay attention to maintaining a positive attitude to a certain extent, and the patient's family should also give appropriate psychological support.

Generally, when there is such an auspicious situation, you can properly carry out physical exercise, and then supplement the protein and other nutrients necessary for the human body, so that Qi Lu Cave can effectively improve the high dryness.

Muscular dystrophy is a hereditary disease caused by mutations in muscle genes that cause muscle fibers and muscle cells to be unable to maintain normal physiological functions, gradually deteriorate, die, and lose, resulting in muscle weakness and atrophy. Muscular dystrophy is a genetic disorder. Currently, there are very limited methods for this genetic disorder.

There are many muscular dystrophys that do not have specific drugs, but it does not mean that there are no drugs**, such as Duchenne muscular dystrophy, which is the most common muscular dystrophy, and progressive muscular dystrophy, which is the most common muscular dystrophy. In the early stages of the disease, at the age of 2-3 years, patients can be given hormones** as early as possible. Corticosteroids can effectively reduce the time of respiratory muscle weakness and delay the time of paralysis in bed.

In addition, there are drugs such as high-dose idebenone that may have a potential ** effect on patients. At present, humans are still developing genes for these patients**. For example, the deletion of exon 51 manifests as progressive muscular dystrophy.

There is a drug called exon 51 skipping, which can skip exon 51 and express relatively normal proteins, which has achieved quite good results in many children. This drug is constantly being developed, and there will be more and more ways to target this disease in the future. Other muscular dystrophy diseases are facing the same situation, and corresponding specific or potentially effective drugs are constantly being explored and developed.

Muscular dystrophy is mainly symptomatic. There is currently no specific treatment for muscular dystrophy. Muscular dystrophy is a genetic disorder.

As a result of genetic defects, a group of proteins that maintain the structural and functional stability of skeletal muscle cells become abnormal, leading to muscle weakness and atrophy. Hereditary diseases generally cannot be reached**, and corresponding symptomatic ** needs to be given when the patient has symptoms. A combination of exercise, occupation**, language, respiratory, medications, surgery, etc., can improve patients' symptoms.

If the patient can be given hormones**, hormones** can effectively relieve the patient's symptoms and ensure the quality of daily life. In addition, it can also give the patient energy supplements, etc.

So far, muscular dystrophy has no specific effect**, only symptomatic and supportive**, and patients can increase nutrition and normal activities.

Muscular dystrophy is a group of genetic disorders characterized by progressively worsening myasthenia gravis and degeneration of muscles that govern movement. It's about genes. There is no specific medicine, mainly proper exercise, massage, and acupuncture with caution.

Muscular dystrophy is non-specific** and can only be symptomatic and supportive**, such as increased nutrition and normal activities. Physical and orthopedic forms prevent and improve spinal deformities and joint contractures, and are important for maintaining motor function. Drug**1, Coenzyme Q10Coenzyme 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 cycle of cyclic muscular dystrophy is generally 1-3 months, but there may be individual differences depending on factors such as the severity of the disease, the regimen, the timing, and the individual's physique.

**Cost** There can be obvious individual differences, and the specific cost is related to the selected hospital, **plan, medical insurance policy, etc. Prognosis is generally prognosis: muscular dystrophy progresses gradually due to the lack of specific methods, and most of the prognosis is poor.

Patients with DMD are unable to walk until age 12 and often die of respiratory failure or heart failure in their 20s. Because there is no specific method for this disease for the time being, the purpose of nursing is to try to keep the condition from worsening, or to slow down the progression of the disease. Psychological care should maintain a positive attitude, consult a psychologist when necessary, take medication according to the doctor's instructions, and do not stop without authorization.

Follow-up InstructionsRegular check-ups to monitor the progress of the disease in real time.

Disease analysis: **Muscular dystrophy can mainly be treated by taking the method of combining traditional Chinese and Western medicine, using drugs according to the condition, and secondly, acupuncture and full joint mobilization can also be used to regulate. The cause of muscular dystrophy is considered to be caused by genetic abnormalities, deterioration of muscle cell membrane stability, and loss of muscle cell membrane function.

Suggestions: During the period, the nutrition in the diet should be strengthened, it is advisable to eat easy-to-digest food, eat less and more meals, not eat too spicy and salty food, and exercise as much as you can, but not overwork. Usually pay attention to prevent contractures, you can apply local hot compresses to promote blood circulation, pay attention to maintaining a good mental state, maintain a good environment, and prevent the further development of the disease.

It's a conundrum.

Muscular dystrophy cannot be done, and there is no specific method for muscular dystrophy so far, but only symptomatic and supportive, such as increased nutrition, normal activities, physical and orthopedic, which can prevent and improve spinal deformities and joint contractures, which are important for maintaining motor function. Because it is a lesion of the muscle itself, especially for patients with rapid progression, it is not encouraged to do more strenuous exercise to avoid aggravating the condition, but patients can be advised to move appropriately, and can not stay in bed for a long time, ** drugs can be coenzyme Q10, ATP and vitamin E. Since there is no effective method, it is important to detect carriers, perform prenatal diagnosis and abortion of sick fetuses.

It is recommended to seek medical attention and let the doctor arrange the ** plan, and the patient actively cooperates.

Muscular dystrophy is a rare genetic disease, and there is currently no best way, but there are some ways to alleviate symptoms, delay disease progression, and improve quality of life. Here are some common methods::

1.Nutritional support**: Patients with muscular dystrophy need a high-calorie, high-protein diet to replenish the nutrients their body needs.

2.Cover preparation**: including muscle exercises, massages, physiotherapy, etc., can help build muscle strength and relieve muscle atrophy.

3.Medications**: Drugs that promote muscle growth, drugs that improve muscle fatigue, etc., can relieve symptoms and improve quality of life.

4.Genetic**: currently being studied, it may be an effective means of muscular dystrophy in the future**.

The effect varies from person to person, and it is necessary to formulate a plan according to the specific situation of the patient. It is advisable to seek medical attention as soon as possible and seek help from a medical professional.

1. Effectively repair the muscle nerve cells in the muscle lesion site, induce or activate the muscle cells in the dormant and inhibited state in the muscle lesion site to differentiate and proliferate, and promote the redevelopment of human tissue and muscle tissue.

2. Improve the living environment of muscle cells, improve nerve conduction dysfunction, and restore muscle innervation function.

3. Improve the limb function of muscular dystrophy patients, restore dynamic balance, and realize the role of patients moving freely.

What are the symptoms of muscular dystrophy.

1. Obvious atrophy and weakness of neck muscles, brachial muscles, shoulder girdle muscles and other parts, obvious atrophy of humeral muscles and shoulder girdles, and obvious bulges on both sides of acromion, and some patients will also have gastrocnemius hypertrophy.

2. Walking disorder, which worsens with the age of the patient, which in turn causes the patient's Achilles tendon contracture, pterygoid shoulder, myocardial hypertrophy, lung infection, etc.

3. Pelvic girdle muscle weakness, atrophy, and muscle contracture.

4. Distal muscle contractures, drooping eyelids, etc.

The overall ** of muscular dystrophy is long-term persistent**, and it also takes more than 1 year after the symptoms are controlled. Generally, symptomatic support is the mainstay, drugs are mainly vitamin E, inosinate, nicosamide, and others**training are the mainstay.

1. Drugs**.

1. Vitamin E:

It is one of the commonly used antioxidants, and the main purpose of the application in this disease is to relieve the symptoms of muscle wasting and promote the control of the disease.

2. Inosine: It can improve the body's protein and ATP levels, thereby relieving muscle weakness and atrophy, and is an important adjuvant drug for this disease.

3. Lingspori polysaccharide Zhaoba injection:

The main effects are atrophic myotonia and progressive muscular dystrophy, as well as related immune deficiencies and other symptoms, which can effectively control the disease process.

4. Nicoshami:

It is a commonly used respiratory stimulant that can control symptoms in time during the acute onset of respiratory failure and avoid life-threatening conditions.

2. Surgery**.

Complications such as joint contractures and spinal deformities caused by muscular dystrophy and complications such as cataracts can be surgically performed**.

3. Others**.

Mainly to carry out ** training, it is known that the old muscle weakness and muscle atrophy can lead to a significant decrease in the patient's mobility, and timely **** can alleviate muscle weakness and slow down the course of the disease.

Muscular dystrophy is a hereditary muscle degenerative disease, and many friends feel that they can only wait when they talk about genetic diseases. In fact, there are many types of muscular dystrophy, and the severity of the disease and the age of onset vary greatly between the various types. If done properly, most patients can live longer.

But muscular dystrophy is not a simple matter, but a system engineering, including drugs, improving strength, as well as training and protecting joints. In addition, it is necessary to delay the deformation of the spine, reduce bone loss, and even delay the degree of damage to the respiratory and heart muscles, so it is necessary to find a professional to standardize**. Some experts in the Western medicine family are also using glucocorticoids, commonly used such as prednisone, deflurode, methyl spiked nylon, etc., so glucocorticoids are also a choice.