How is progressive muscular dystrophy treated? Can it be cured?

Go to a regular hospital to see an occupational doctor. Netizens are not professional doctors and are unreliable.

Progressive muscular dystrophy, muscle weakness is mainly manifested as bone weakness, easy fatigue, and severe manifestations are difficulty in drinking water, so can muscle weakness be cured? To trust the current medical technology and build confidence that it will get better, here are some ways to share it. Tool Raw Materials Optimistic and Comfortable Environment Method Step by Step Reading 1 5 First of all, you must maintain an optimistic attitude, be happy, and maintain a joyful mood, you can listen to some cross talk, watch some comedy movies.

It is important to get rid of pessimistic and negative thoughts, so that the condition can be greatly improved, so that you can recover your health faster. 2 5 Change an environment, if possible, choose a beautiful environment, fresh air environment, cultivate sentiment, can promote health, living environment to maintain ventilation, comfortable. Stay away from irritating things as much as possible.

3 5 You can participate in appropriate social activities to divert your attention and achieve the goal of relaxing your muscles and invigorating your blood, 4 5 If possible, do some appropriate exercises, or ask for the help of family or friends, do some exercises within your ability, but to prevent too much strenuous and hurt yourself. 5 5 Seek the help of a professional doctor, according to the severity of the condition, use the corresponding **, but be careful not to rely on the drug for a long time, it will cause ***. More need for your own confidence and a happy mood.

Muscle weakness can occur in a variety of disorders, and the method of causing it varies depending on the disorder. If it is caused by hypokalemia, the patient generally presents with muscle weakness in the proximal extremities, mainly potassium supplementation**, patients with mild symptoms can take potassium chloride extended-release tablets orally, and in severe cases, potassium can be pumped intravenously**. If the patient has Guillain-Barré syndrome, there may also be weakness in the limbs, and there will be sensory impairment in the limbs, and adrenocorticosteroids can be used in the early stage, generally dexamethasone and prednisone, and drugs to trourve the nerves, such as vitamin B12 and methylcobalamin, and plasma exchange if necessary**.

If caused by myasthenia gravis, patients typically present with weakness in the proximal extremities, most of which are mild in the morning and severe in the afternoon. If the patient has thymoma or thymic hyperplasia, thymus surgery** or radiation**, and if necessary, cholinesterase inhibitors are given at the same time**, and in the absence of thymoma and thymic hyperplasia, drugs are mainly used**.

Progressive muscular dystrophy is a hereditary disease in which muscle cells are structurally abnormalized during the growth of muscle cells due to genetic abnormalities, resulting in incomplete muscle cell membranes.

The structure of muscle cells is destroyed, which is manifested by muscle weakness and atrophy, incomplete muscle cell membranes, and creatine kinase entering the bloodstream.

This is a hereditary disease, and there is currently no way to deal with the symptoms, and there is no good way to deal with its pathogenesis.

It is expected that in the future some kind of genetic intervention** will be discovered that can completely change the disease**.

Drugs**.

Due to individual differences, there is no absolute best, fastest and most effective medication, except for commonly used over-the-counter drugs, the most appropriate drug should be selected under the guidance of a doctor in full combination with individual circumstances.

Glucocorticoids.

It is used in children with confirmed Duchenne muscular dystrophy and is generally not used for milder forms such as Becker muscular dystrophy.

It is recommended to start standardized oral administration after 3 years of age and before motor function becomes abnormal**.

Oral administration daily after breakfast.

Prednisone or prednisolone, one dose at a time.

Depending on the effect and the situation, it can be changed to weekends or intermittently.

Standardized hormones** can delay disease progression, prolong survival years, and effectively reduce the incidence of scoliosis in children.

For heart damage, respiratory tract infections and gastrointestinal dysfunction, use relevant drugs under the guidance of a doctor.

Other drugs that may be available include ATP, inosinate,

Vitamin E calcium,

Coenzyme Q10, etc.

** Methods of progressive muscular dystrophy.

1. Basic methods: including a series of traditional Chinese medicine preparations-based drugs**, traditional Chinese medicine decoction, moxibustion and massage methods should be applied at all stages of the disease, and more than 10 kinds of clinical preparations have been developed that can be applied to patients with different syndrome types.

2. Training methods: including muscular dystrophy exercises and tendon training methods. The tendon** training method has developed different methods for each period of the disease, including tendon flexion and extension training, standing muscle training, and moving training.

3. Physics: There are mainly leveling instruments, traditional Chinese medicine instruments and self-made splints, self-made simple joint splints, which are used to fix the knee joint and ankle joint to assist in training.

Progressive muscular dystrophy is a rare, hereditary disorder, also known as duchenne muscular atrophy, caused by a genetic mutation that disrupts muscle protein synthesis. There is currently no complete way to develop progressive muscular dystrophy, but a series of methods can be used to help patients relieve symptoms, delay the progression of the disease, and improve quality of life.

Commonly used methods include:

1.Confirm the diagnosis: progressive muscular dystrophy requires genetic testing and other methods to confirm the diagnosis.

2.Physical**: such as massage, physiotherapy, traction and other means, can be used to relieve muscle stiffness and enhance muscle strength.

3.Medications**: Some medications can help relieve muscle spasms and preserve muscle function, such as adrenocorticosteroids, cholinesterase inhibitors, etc.

4.Assistive devices, such as wheelchairs, crutches, walkers, etc., can help the patient to move.

5.Respiratory**: Such as a ventilator, which can help patients maintain normal breathing.

In summary, although there is no complete method for progressive muscular dystrophy, timely treatment can help patients alleviate symptoms, delay the progression of the disease, and improve the quality of life. If you or your family members have relevant symptoms, it is recommended to seek medical attention as soon as possible and receive professional treatment**.

1.Medications**: Hormones can delay the progression of the disease and reduce the incidence of scoliosis. Other drugs such as ATP, inosine, vitamin E, calcium, coenzyme Q10, etc. can be used according to the situation.

2.**Imitation Mask Training: It is very important to standardize the family **** to be able to maintain a better life performance and posture. Instruments** such as standing inclined plates, foot orthopedic braces, etc. also play an important role.

3.Surgery: For problems such as scoliosis, joint contractures, etc.

Progressive muscular dystrophy is an inherited muscle disease that can be divided into pseudohypertrophic muscular dystrophy, facicoscapulohumeral muscular dystrophy, and oculopharyngeal muscular dystrophy. At present, there is no particularly good way to develop progressive muscular dystrophy, and although new drugs have been developed, they are expensive and have limited efficacy. The new drug is mainly aimed at the skipping nature of exons**, and at present, it is mainly based on the general symptomatic **, and can be given vitamin E, adenosine triphosphate, idebenone and other drugs**, but the efficacy is limited.

In addition, **training, including joint movement, acupuncture, massage, etc. In short, there are currently very limited and no methods for progressive muscular dystrophy, and symptomatic support is generally used. There is no cure for progressive muscular dystrophy at the moment.

It is mainly symptomatic and supportive, and can be properly trained. Try to maintain the patient's ability to walk independently, prolong the time of independent walking, and improve the quality of life. Low-dose glucocorticoids can lower serum creatine kinase levels but do not slow disease progression.

At present, some ** methods are still in the experimental stage, such as gene replacement**. The diet should be balanced and nutritious. Pay attention to proper exercise and avoid overwork.

It can enhance resistance and reduce complications. You can try to use energy-boosting medications, such as idebenone and inosinate tablets. There is no cure for progressive muscular dystrophy at the moment.

It is mainly symptomatic and supportive, and can be properly trained. Try to maintain the patient's ability to walk independently, prolong the time of independent walking, and improve the quality of life. Low-dose glucocorticoids can lower serum creatine kinase levels but do not slow disease progression.

At present, some ** methods are still in the experimental stage, such as gene replacement**. The diet should be balanced and nutritious. Pay attention to proper exercise and avoid overwork.

It can enhance resistance and reduce complications. You can try to use energy-boosting medications, such as idebenone and inosinate tablets.