What is the best treatment for motor neurons?

The disease is not known so far, some scholars believe that it is caused by chronic viral infection, and the disease is slowly and progressively aggravated after the onset of motor neurons, and there is no specific measure to stop the progression of the disease, and patients often have complications in the later stage.

If you can take care of it carefully and strengthen the symptomatic support complex**, you can minimize symptoms and prolong life. Advise all relatives to go to a neurological disease specialist for diagnosis and treatment after the onset of the disease.

Nutritional deficiencies and metabolic disorders polyneuritis**Primary motor neurons, diabetes should pay attention to blood sugar control, uremia with hemodialysis and kidney transplantation, myxedema with thyroxine. Tumors are surgically removed; Corticosteroids may be used for collagen disease SLE, scleroderma, rheumatoid arthritis, and neuropathy after serum injection or vaccination**.

In addition to these, you can also use Chinese medicine**. The onset of motor neuron disease is mainly related to acquired dystrophy, spleen and stomach dysfunction, and congenital endowment liver and kidney deficiency. The spleen is the main meat, and patients with insufficient spleen will have weak muscles; The main muscles and bones of the liver will be manifested in the claws, liver yin deficiency, and meridian dystrophy, which will show the appearance of limb confinement; Patients with kidney qi deficiency will have soreness in the waist and knees and weakness of the limbs.

Traditional Chinese medicine** is mainly to regulate the function of the spleen and stomach, nourish the liver, nourish the kidney, and replenish the essence.

Motor neuron degenerative disease is a chronic neurocannibalization disease, which is more difficult in the later stage of the disease, and its severe onset can invade the anterior horn cells of the spinal cord and the nerve nucleus of the brainstem and the pyramidal cells of the motor cortex of the brain, resulting in dyspnea and dysphagia and life-threatening, about 5%-7% of patients are caused by abnormal genetic immunity or viral infection. The remaining patients** are unknown, but have been reported to be related to heavy metals, chemical poisoning, and the surrounding environment. The efficacy of simple drugs is not good, the condition is difficult to control, and the disease leads to mental dystrophy and gradually aggravates the secondary deficiency and neurological impairment, so that the neurological symptoms are further aggravated and life-threatening.

Solution: Hormones have little effect on the disease, Chinese medicine dialectical treatment, enhance the body's immune function, improve the body's ability to resist disease, the combination of traditional Chinese and Western medicine to expand the microcirculation of the affected nerves to nourish the nerves, so that the damaged residual nerves get sufficient blood supply to prevent the disease from continuing to develop. And the use of nerve regeneration drugs to stimulate and activate the paralytic shock of the nerve complex ** to innervate and regulate movement and various functions to recover and improve

You need to help send medical history, medical records, and examination materials for your guidance.

It is recommended to use traditional Chinese medicine**.

It is recommended to use traditional Chinese medicine** for good results.

At present, there is a lack of effective measures for motor neuron disease, and it is of great significance for patients to support and symptomatize. Exercise and physiotherapy can delay the progression of amyotrophy and pay attention to preventing joint contractures. Patients with dysphagia should be fed as soon as possible to ensure nutrition** and avoid aspiration pneumonia caused by aspiration.

Intermittent positive pressure (PAAP) may be considered for patients with significant dyspnea. Motor neuron disease is a heterogeneous disease, with a variety of pathogens and no influence on each other, so it must be used in combination with a variety of methods, including various non-drugs.

**Method: 1. Respiratory support. When patients with motor neuron disease have respiratory disorders, endotracheal intubation or tracheostomy is often used, among which non-invasive ventilation is more common, assisted by ventilator ventilation, and the patient's ventilation function is regularly monitored.

In addition, positive airway pressure can be used to manage nocturnal hypoventilation, reduce patient mortality, and improve quality of life.

2. Nutritional support. Patients should pay attention to eating high-calorie, high-protein foods daily. If the survival of the patient is seriously affected due to swallowing dysfunction, enteral nutrition under the guidance of medical staff is the best method, and the gastrointestinal nutrition of percutaneous endoscopic gastrostomy can significantly prolong the survival of the patient.

3. Symptomatic**. Symptomatic treatment is based on the patient's symptoms, which can treat complications symptomatically and improve the patient's quality of life. Muscle cramps can be treated with antiepileptic drugs; Patients with urination and defecation disorders can use drugs such as senna and lactulose under the guidance of a doctor; Patients with anxiety symptoms can be given drugs such as haloperthioxine and melitrexime under the guidance of a doctor; Patients with sleep disorders can be given drugs such as amitriptyline, zolpidem, levopiclone, etc., under the guidance of a doctor.

Motor neuron disease is mainly based on deficiency, and its ** should follow the principle of making up for the deficiency, and it is divided into the following types according to the different pathogenesis

First, liver and kidney yin deficiency type. The most common clinical type is liver and kidney yin deficiency, and the symptoms are limb muscle atrophy, especially the distal hand, which is often eagle claw or ape palm.

Second, yin deficiency and fire prosperity type. Symptoms include slicing palms, dry muscles, grooves between muscles, weakness in grasping things, or muscle tremors.

Third, spleen and kidney yang deficiency type. Symptoms include limb weakness, fatigue, muscle wasting, relaxation, mental exhaustion, and shortness of breath and paleness.

Fourth, qi deficiency and blood stasis type. Symptoms include weakness of fingers and muscles, fatigue, limb fatigue, night sweats, palpitation, and dry mouth.

The above types are not completely separated, they are all mixed with each other in ordinary times, and a variety of ** methods need to be flexibly used in clinical evidence.

1. Drugs**.

When patients have MND, vitamin E and vitamin B can be taken orally, in addition to coenzyme intramuscularly, citicoline intramuscularly, etc.**. In addition, diazepam can also be used for muscle spasms when patients have muscle spasms. In addition, it is also recommended to have a conditioning method, that is, to strengthen the muscles to return to the original soup**, which can play a role in improving motor neuron cells and preventing muscle deformation, and can also dredge the meridians in the body, regulate the liver, spleen and kidney function in the body, and when the patient's physical symptoms improve, it can dredge the blood circulation in the patient's body, enhance its immune function, and gradually improve the symptoms of stiffness and weakness in the limbs.

2. Surgery**.

When the patient is ventilated paralyzed, a ventilator is needed to assist breathing.

3. Others**.

In recent years, stem cell technology has been developing, providing the best opportunity for motor neuron disease, therefore, stem cells have also become one of the means of motor neuron disease, through which the disease can be effectively alleviated and improved.

There is still a lack of drugs that can effectively reverse or control the progression of the disease. The motor neuron disease pathogen is diverse and affects each other, so it must be a combination of multiple methods. The ** of motor neuron disease includes **, symptomatic ** and various non-pharmacos**.

1. General**.

1. When patients have muscle cramps, antispasmodic and analgesic drugs can be used for symptoms.

2. When the patient's condition progresses and respiratory failure occurs, a non-invasive ventilator can be used as soon as possible to assist breathing, or whether to undergo tracheostomy and mechanical ventilation according to the specific situation.

2. Drugs**.

Riluzole: inhibition of glutamate release has the potential to delay the course of the disease and prolong the survival of patients with bulbar palsy, but there is no significant improvement in muscle strength and quality of life.

3. Psychology**.

Patients with motor neuron disease are likely to have anxiety and depression, and psychological counseling should be strengthened, and anti-anxiety and depressive drugs can be given if necessary. If the patient has sleep disorders, he should be given psychological **, and sleep aids such as zopiclone and zolpidem should be given as appropriate.

4. Others**.

1. Recent studies have shown that neural stem cell transplantation, gene ** and other methods may have a certain effect on motor neuron disease, but they are still in the research stage and are not widely used in clinical practice.

2. Acupuncture, massage, physiotherapy and other traditional Chinese medicine can be used to improve the patient's limb condition.

In motor neuropathy**, B vitamins can be used to nourish the nerves. Riluzole has the effect of inhibiting the release of glutamate, can delay the course of the disease, and prolong the survival of patients with bulbar paralysis (characterized by laborious swallowing, choking on drinking water, and dysarthria), but regular blood and liver function tests are required during the application, and the symptoms of bulbar paralysis have improved in some cases after application, but it is of little help to patients with limb weakness and muscle atrophy. MND also needs to be symptomatic**, with appropriate pain relief and nutritional support for symptoms such as nutritional disorders and spasm pain.

Patients with feeding difficulties may be given a nasogastric diet**.

Motor neuron disease (MND) is a group of chronic, progressive neuromorphic disorders of the anterior horn cells, brainstem motor neurons, cortical pyramidal cells, and pyramidal tracts of the spinal cord by unknown choice.

MND** is not well understood, but it is thought to be caused by the exposure of genetically susceptible individuals to adverse environments with age, i.e., a combination of genetic and environmental factors contribute to the development of MND.

For motor neuron disease, you can start from the following aspects:

First, oral vitamin E and vitamin B group.

Second, coenzyme intramuscular injection, citicoline intramuscular injection, etc., can be used intermittently.

Third, diazepam can be used orally for muscle spasms, and chlorphenabutyric acid can be taken in divided doses.

Fourth, some drugs can be used for this disease, such as thyrotropin-releasing hormone, interferon, lecithin, and testosterone.

Fifth, with the recent development of cell technology, stem cells have become one of the means of the disease, which can alleviate and improve the disease.

Sixth, the affected limb is massaged passively.

7. Prevention and treatment of lung infections.

8. Patients with respiratory muscle paralysis should be ventilated to assist breathing.

Every person with MND has a different condition and needs to be tailored to the individual.

MND can manifest as weakness and atrophy of the limbs, clumsiness and weakness of finger movements, muscle weakness and atrophy over the course of the disease, extending to the trunk and neck, and finally involving the facial and throat muscles. Patients may have bulbar paralysis, mostly in the late stage, the tongue muscles are first involved, manifested as tongue muscle atrophy, fasciculation, and tongue protrusion weakness, followed by pharyngeal, laryngeal, and masticatory muscle atrophy and weakness, resulting in the patient's slurred arthria, dysphagia, chewing weakness, and the orbicularis oculi muscle in the facial muscle is more obviously involved. There is often a pattern of disease progression in MND, usually from the upper extremity that is first affected, then to the contralateral upper extremity, to the ipsilateral lower extremity, to the contralateral lower extremity, and finally to the bulb involvement.

Motor neuron disease can be life-threatening, mostly within 3 to 5 years, death from respiratory muscle paralysis or lung infection, so motor neuron disease is more harmful. You can come to Beijing Renxuan Traditional Chinese Medicine to find Sheng Jinqiangfu**, and through one-to-one conditioning of Yiyuan Muscle Formula, the patient's symptoms can be improved.