Can arm weakness caused by ALS be recovered?

ALS can not be completely **, but after effective **, it can prevent the aggravation of ALS and prolong the survival cycle of patients, and the main **method is symptomatic**.

If the patient is drooling frequently or has a lot of phlegm, oral antihistamines and expectorant drugs can be used to control it. Patients who are unable to eat normally should be fed a nasogastric diet. If the patient has difficulty breathing, oxygen may be given or a ventilator may be used to assist breathing.

When respiratory failure occurs, a tracheotomy is done to open the tracheotomy and an artificial ventilator is used.

Patients should also be turned over and patted on the back frequently in daily life to prevent bedsores and pneumonia and other diseases.

At present, there is no way to ** this disease, that is, ALS cannot be **.

Hello friends! At present, the medical level has not reached the complete ** of this disease, so there is no way to ** ALS at present, and ALS cannot be completely **. Therefore, ALS is an undead cancer.

Not completely**, ALS is an undead cancer.

Hello, ALS is a motor neuron disease, which is a group of diseases with chronic paralysis caused by unidentified and progressive neurodegeneration. The disease is recognized worldwide as a terminal illness with no cure**. The general natural course of the disease is 3 to 5 years, and finally death due to respiratory muscle weakness, respiratory failure, complications such as asphyxia, pneumonia.

Long-term exercise for ALS generally has a certain effect, and whether it is effective needs to be analyzed according to the period of onset of ALS, and there are certain differences. ALS is a type of motor neuron disease, which is prone to the gradual atrophy of muscles throughout the body, which affects motor function, and later affects swallowing and pronunciation.

1. Early stage of the disease: In the early stage of ALS, muscle atrophy is usually not particularly obvious, and long-term exercise can delay muscle atrophy, improve muscle strength, and maintain motor function, so it is more effective;

2. The middle stage of the disease: in the middle stage of the onset of ALS, muscle atrophy will usually be more obvious, which usually has a greater impact on the patient's motor function, and will have a certain effect through long-term exercise, but it may not be able to achieve complete improvement effect, and the patient is prone to inconvenience and even inability to take care of himself;

3. Late stage of the disease: when ALS is in the advanced stage of the disease, usually the muscle atrophy is serious, and the general patient will be in a state of bed rest, losing the voluntary motor function, and the way of long-term exercise is not very effective, but it is necessary to insist on long-term exercise, and maintain the range of motion of the joints as much as possible through passive movement.

The specific cause of ALS is not clear, and there is no specific clinical method to achieve a good effect, and the condition will progressively worsen. In the early stage, the function can be maintained through the way of sports training, and in the later stage, attention should be paid to nursing and prevention of complications.

ALS is also ALS, how does this disease work**, it is a disease of nervous system degeneration, there is no specific drug, if the doctor diagnoses this disease, it may occur gradually, and then gradually appear muscle atrophy, muscle weakness, and generally muscle tremors and other symptoms. According to the onset of the disease, such as genotyping, which type it is, and then what are the clinical manifestations, some people progress very slowly, some people progress relatively quickly, and each patient's muscle atrophy and muscle weakness are different, such as respiratory muscle weakness, and a comprehensive judgment is made.

If it is relatively early, it can be used with liraglutide drugs**, and then use vitamin B to nourish the nerves, which can be assisted by traditional Chinese medicine at any time. If ALS has respiratory muscle weakness, the main thing is to save the respiratory muscle weakness, and ventilator-assisted ventilation should be used to maintain relevant vital signs.

Amyotrophic lateral sclerosis (ALS), also known as ALS, is a chronic, progressive degenerative disease that affects upper and lower motor neurons and their innervated trunk, limbs, and head and face muscles. It often manifests as progressive aggravation of muscle weakness, muscle atrophy, and fasciculations caused by damage to upper and lower motor neurons.

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