Will ALS people lose their ability to take care of themselves?

ALS sign is a common name, mainly refers to amyotrophic lateral sclerosis sign, is a congenital disease, patients will have progressive muscle weakness, limited activities, and gradual loss of self-care ability, is caused by spinal cord motor neuron damage, early patients can have limb movement disorders, advanced patients can have respiratory failure, difficulty swallowing, difficulty in speech expression, gradual loss of muscle function, patients are extremely painful, because consciousness is awake, but can not control physical activities.

The dangers of ALS.

1. Early manifestation, the early symptoms of ALS are not very obvious, patients usually only feel weakness in the body, easy fatigue, slurred speech, shoulder soreness, and slight numbness of body parts.

2. Medium-term performance: In the middle stage of ALS, the muscles of patients with ALS begin to gradually atrophy, which is manifested as difficulty in movement, strange facial expressions, and speech disorders, which eventually lead to muscle emaciation and atrophy of the whole body.

3. In the late stage, after muscle atrophy, the patient completely loses his speech ability and mobility, resulting in paralysis of the whole body, difficulty breathing, and finally respiratory paralysis and suffocation.

Ways to prevent ALS.

1. Pay attention to a balanced diet and food hygiene, eat more vegetables and fruits, consume more protein-rich foods and supplement vitamins to ensure adequate intake of carbohydrates and trace elements.

2. Pay attention to maintaining a happy mood, stay optimistic and positive, and not be too nervous and worried.

3. Proper exercise can enhance physical fitness and improve immunity.

Yes, people with ALS must slowly lose their ability to take care of themselves, which is very pitiful, and will be motionless in the end, so if you have this disease, it is also a terminal illness at present.

Does Meniere lead to the ability to take care of oneself in practical life? It depends on the development of the individual, if some people develop well, the medical ** will not be like this.

Ordinary people can also get ALS. Amyotrophic lateral cords

Hardened ** so far not zhi

Bright. 20% of cases may be DAO

Relating to heredity and genetic defects. In addition, some environmental factors, such as heavy metal aluminum poisoning, may cause motor neuron damage. The main theories of the causes of motor neuron damage are:

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

2.Free radicals damage nerve cell membranes.

3.Nerve growth factor deficiency prevents nerve cells from growing and developing sustainably.

Early symptoms are mild and can be easily confused with other diseases. Patients may only feel some symptoms such as weakness, flesh jumping, and fatigue easily, and gradually progress to generalized muscle atrophy and difficulty swallowing. Respiratory failure develops.

According to the clinical symptoms, it can be roughly divided into two types:

1.Limb-onset type.

Symptoms begin with progressive atrophy and weakness of the muscles in the limbs, and finally respiratory failure.

2.Bulbar onset.

Difficulty swallowing and speaking begins with early progression, and respiratory failure soon progresses.

Hello, the only risk factors that determine DU are age and family history, and the disease has a distinct retrospective genetic trait, following a common chromosomal dominant inheritance pattern. There is growing evidence that smoking is also a risk factor for the disease, as are people who participate in military service, agricultural work, factory work, heavy physical labor, exposure to pesticides, welding, heavy metals, plastics industry work, repetitive muscle use, professional football, trauma, and electrical injuries. People who are exposed to mercury, lead and aluminum from heavy metals have a relatively high incidence of the disease.

The above content is for reference.

Anyone can suffer from ALS, and ALS is a motor nerve.

A type of meta-disease. Motor neuron disease is mainly divided into amyotrophic lateral sclerosis, gyrus.

There are four major categories of progressive spinal muscular atrophy, primary lateral sclerosis, and progressive bulbar palsy. In 20% of cases, it may be related to heredity or genetic defects. In addition, some environmental factors, such as genetics, heavy metal poisoning, etc., may cause motor neuron damage, and it is difficult to have a clear explanation.

Early patients should keep exercising to prevent injuries and maintain an appropriate amount of activity!

The only identified risk factors are age and family history, and the disease has a distinct genetic profile that follows an autosomal dominant inheritance pattern.

Abstract The incidence of ALS is not very high, between 40 and 60 years old, and it is more likely to develop the disease. This disease affects the patient's motor function, language function. Usually you must maintain a good attitude, the diet is suitable for eating light and easy-to-digest food, fresh fruits and vegetables, and avoid eating some greasy and spicy food.

There are not many people who get ALS.

The incidence of ALS is not very high, between 40 and 60 years of age, and it is more likely to develop the disease. This disease affects the patient's motor function, language function. Usually you must maintain a good attitude, the diet is suitable for eating light and easy-to-digest food, fresh fruits and vegetables, and avoid eating some greasy and spicy food.

Yes, the state doesn't know about this at the moment.

Usually there are certain factors between this disease and family inheritance, so can you please tell us what causes this ALS in general?

A small number of cases are genetic, but the majority of cases** are unknown. At present, the risk factors that may be related to the occurrence of the disease include: genetic factors, lifestyle (such as smoking), toxic exposure (such as exposure to organic solvents, pesticides, heavy metal elements, etc.), occupation (such as excessive manual labor), low body mass index, history of head trauma, metabolic diseases, autoimmune dysfunction, viral infection, and neuroinflammatory reactions.

Oh, to put it bluntly, this disease is caused by muscle atrophy.

Yes, this only shows that everyone still needs to exercise more every day.

Yes, dear, and I want to ask about the fact that adults will be limited in playing games in the future, is this news true?

There is no news released by Kiss at this time.

Actually, I personally think it's fake, because you see that e-sports has become a sport, and if adults have restrictions, those e-sports players can't play anymore, so this e-sports competition can't be held, you say, yes, anyway, I personally think it's fake, what do you say?

I personally think so, too.

Now I don't know which people are more susceptible to ALS, ALS is a disease of motor neurons, if you have this disease, there may be muscle atrophy, and then slowly respiratory function will fail, and swallowing function will be slowly lost, this disease is likely to have something to do with their own genetics and genes, but now it is not certain what the specific cause is.

First of all, we should establish a positive and optimistic attitude. Strengthen emotional communication with family members and pay attention to daily care. Provide an adequate nutritious diet based on liquid and semi-liquid foods, and strengthen exercise and massage of atrophic muscles.

Oral drugs can be used to exert force, and traditional Chinese medicine can also be used to carry out a combination of traditional Chinese and Western medicine**.

Guidance: For ALS patients with impaired swallowing function, the diet is mainly a liquid semi-liquid diet with high protein and high nutrition, rich in energy, meals can be cut with scissors to make vegetable puree, drink more bone broth nutritious porridge, etc., and eat less and more often, you can add protein powder nutrient solution, nasogastric feeding, and early gastrostomy.

ALS is motor neuron disease, which is a neurodegenerative disease in which patients will experience symptoms such as muscle weakness, muscle atrophy, meat jumping, dysphagia, dysarthria, etc., generally without sensory impairment, and may eventually involve respiratory muscles, resulting in dyspnea symptoms. There are four types, the most common type is amyotrophic lateral sclerosis, followed by progressive bulbar palsy, progressive spinal muscular atrophy, and primary lateral sclerosis. ALS** is not yet clear, but studies suggest that it may be related to viral infections, autoimmunity, environmental factors (exposure to substances such as lead), genetic factors, and nutritional deficiencies (vitamin B1, etc.).

In terms of prevention, it is necessary to pay attention to rest, avoid fatigue, live a regular life, and do not stay up late. Strengthen nutrition, proper physical exercise, strengthen physical fitness, and avoid infection.

ALS is one of the relatively rare diseases, and the symptoms of ALS may begin as the inability to hold chopsticks in the hand, or fall for no reason while walking, and some may start with a hoarse voice without any obvious symptoms. In this case, a neurologist must do the necessary tests such as electromyography, nerve conduction velocity, and MRI to confirm the diagnosis. In addition, there is no effective plan for ALS, so we can only actively cooperate with doctors to prevent it.

ALS is also known as sclerosis of the amyotrophic lateral cords. It's still unclear. In some cases, it may be due to a genetic defect.

In addition, some patients may be caused by environmental reasons, such as poisoning by heavy metals, which will cause damage to the corresponding parts of the motor neurons. There are two reasons for the damage: 1. Toxic substances, a lot of glutamate accumulates between nerve cells, and nerve cells will be damaged.

2. If there is a lack of corresponding nerve growth factors, then nerve cells cannot grow and develop.

ALS refers to the gradual atrophy of some organs of the body, there is no clear statement in the world, the reason is not clear, the disease is not possible, it is considered to be caused by the damage of upper motor neuron and lower motor neuron, resulting in gradual atrophy of various parts of the body, generally starting from the eyes, gradually from the upper limbs to the lower limbs.

ALS is also known as amyotrophic lateral sclerosis.

This is related to genetic factors, occupation, lifestyle habits, abnormal autoimmune function, metabolic diseases and other reasons.

It seems that it is not very clear at the moment, and it may be related to a genetic defect.

There is some kind of immunodeficiency and motor neuron injury patients due to low autoimmune function, or, once the course of cold is prolonged, the disease is aggravated, the muscle beat is aggravated, and the muscle atrophy is weak, especially the bulbar palsy patients are prone to pulmonary infection, if not prevented and treated in time, the prognosis is poor, and even endangered the patient's life.