Can ALS recover completely? Will ALS be cured?

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.

ALS cannot be treated, but it can be systematically diagnosed and treated to delay the progression of the disease. ALS is a motor neuron disease, also known as amyotrophic lateral sclerosis, mainly because the patient's brain or motor nerve cells have been significantly damaged, resulting in obvious muscle atrophy in the patient, resulting in paralysis of the patient, the body as if it is frozen, and in the early stage, because the symptoms are relatively insidious, so everyone may not know that they have a disease.

ALS cannot be treated, but it can be symptomatic to improve clinical efficacy and improve the quality of life of patients. The most important of these is respiratory support**, when the respiratory muscles are involved and the patient has difficulty breathing, at which point ventilator respiratory support is the most important.

Patients are advised to go to a regular hospital for treatment, follow the advice of a specialist, and be positive**.

ALS refers to amyotrophic lateral sclerosis, the most common type of motor neuron disease. At present, it is not completely clear, considering that it is related to environmental factors, aging and genes, etc., there is no way to use the disease, and only drugs can be used to delay the progression of the disease. In essence, this disease is a degenerative disease of the nervous system, and once it occurs, its condition tends to progressively worsen, and most patients start with small muscles in the hands, and gradually develop weakness and atrophy.

This muscle weakness gradually spreads throughout the body, eventually causing the patient to be unable to swallow and speak normally, and eventually the respiratory muscles will also be affected, resulting in difficulty breathing. Terminally ill patients are often bedridden, require ventilators to help them breathe, and are unable to move muscles anywhere in the body except for the normal movement of the eyeball. Therefore, with the current level of medical treatment, ALS has no way, and it should be mainly to alleviate the patient's discomfort and improve the quality of life.

ALS patients often do not live long, usually not more than 10 years, mainly because ALS patients gradually worsen quadriplegia, oropharyngeal dysfunction, dyspnea, swallowing, choking on drinking water, etc., which can cause aspiration, resulting in uncontrolled lung infection and suffocation and death.

Therefore, the factors that cause death in ALS people are mainly due to the death of complications, and the life expectancy is generally 10 years, but some patients can survive for a long time with good care. There are people who have ALS and are able to survive for a long time with good care and die until they are in their 70s. Therefore, the key is to take care to avoid serious complications such as lung infections and suffocation that can lead to death.

The full name of ALS should be called motor neuron disease, and the main content is called amyotrophic lateral chordate and rolling sclerosis, which covers the lesions of lower motor neuron and upper motor neurons. The main epigenetic manifestations of upper neuron lesions are muscle weakness, muscle rigidity, and tendon hyperreflexia, while the main manifestations of lower motor neuron lesions are muscle weakness, muscle atrophy, and muscle tremor. How long you can live with ALS depends on how quickly the disease progresses, and some can survive for a long time if the disease progresses slowly, remains stable for a long time, or does not affect important muscles.

If the patient progresses very rapidly, quickly causing quadriplegia and paralysis of the throat muscles and respiratory muscles, the life expectancy of such patients will be significantly shortened. In summary, according to the literature, the average survival life of ALS is 5-7 years, the shortest may be 2-3 years, and the longest can reach 10-20 years. On the one hand, it depends on the medical condition, and on the other hand, it depends on the medical conditions at the time to determine how long you can survive.

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 a very rare disease that does not cure itself. ALS is a type of motor neuron disease, also known as amyotrophic lateral sclerosis. The prognosis is poor, with most patients dying from respiratory muscle paralysis or lung infection within three to five years of onset.

Amyotrophic lateral sclerosis is the most common type of MND, with most patients being sporadic, and some may have a family history of genetic history. The patient's first symptom is clumsiness and weakness in one or both fingers, followed by muscle atrophy of the hand, especially the thenar atrophy of the large and small thenar muscles, which gradually extends to the patient's forearm, upper arm, and scapular muscles. Because both upper and lower motor neurons are damaged, patients may experience progressive muscle weakness, muscle atrophy, and fasciculations.

But there are miracles in everything, and if you keep a good mood every day, you may have a good outcome.

ALS is a group of motor neuron diseases, the main type of which is amyotrophic lateral sclerosis (i.e., motor neuroblastic atrophy), because the characteristic manifestation is gradual muscle atrophy and weakness, as if the body is gradually frozen.

ALS is also known as motor neuron disease, the latter name is commonly used in the United Kingdom, Charcot disease in France, and Lou Gehray disease in the United States. In China, amyotrophic lateral sclerosis and motor neuron disease are commonly mixed. It is caused by damage to the upper and lower motor neurons, resulting in gradual weakness and atrophy of the muscles including the bulbar (the bulbar refers to the part of the muscles innervated by the medulla), limbs, trunk, chest and abdomen.

The condition of amyotrophic lateral sclerosis is still unknown. In 20% of cases, it may be related to heredity or genetic defects. In addition, some environmental factors, such as heavy metal poisoning, can cause motor neuron damage. The main theories of the causes of motor neuron damage are:

1. Neurotoxic substances accumulate, glutamate accumulates between nerve cells, and over time, causes damage to nerve cells.

2. Free radicals damage nerve cell membranes.

3. Lack of nerve growth factor makes it impossible for nerve cells to continue to grow and develop.