Motor neurons need to be treated with traditional Chinese medicine

This can be conditioned by using traditional Chinese medicine, but it cannot be cured, only to alleviate the condition, because there is no cure for this disease.

Traditional Chinese medicine** is indeed good.

Traditional Chinese medicine believes that 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. The internal regulation of traditional Chinese medicine is mainly to regulate the function of the spleen and stomach, nourish the liver and nourish the kidneys, and the external auxiliary ** such as acupoint injection is mainly to control the loss and damage of neurons.

Restore the conduction function of the nerve, promote the innervation of the nerve for the muscle and the recovery of nutritional function, and the later drug consolidation is mainly to control the development of the disease and prevent the recurrence of the disease.

Around us, there are people who are constantly diseased and atrophied in their limbs, much like a withering tree. They may be staggering today, but they may be in a wheelchair tomorrow, and by the end of the day, the strength of their limbs gradually disappears, and they can only rely on the movement of their eyes or the slight movement of their lips to convey their emotions and ......thoughts to others

Motor neuron disease (MND) is a worldwide intractable disease, with insidious onset and most of the first symptoms are weakness of the limbs and muscle atrophy. As the disease progresses, it can progressively to increased salivation, dysphagia, and dyspnea; Bulbar paralysis symptoms such as dysarthria, increased salivation, dysphagia, and dyspnea may also occur. The early diagnosis of the disease is difficult and the misdiagnosis rate is high, and the patient's condition can only be diagnosed after a certain period of progression, and there is no effective treatment method so far.

The average survival of patients is about 2-5 years. In general, the younger the age of onset, the longer the survival time.

Western medicine mostly uses riluzole to delay the development of the disease and improve the quality of life of patients, which inhibits neurotrophic neurological drugs, and the disease will continue to progress after taking it without much effect, treating the symptoms but not the root cause, but the drug is expensive, bringing a heavy economic burden to patients and society, and restricting the use of the drug.

In traditional Chinese medicine, we use pure Chinese medicine decoction to strengthen the brain and stop wilting decoction, in order to help the right and dispel evil, consolidate the foundation and cultivate the yuan, treat both the symptoms and the root causes, and formulate the main line of tonifying the kidney and marrow, relaxing the muscles and invigorating the blood and circulation, and the principle of brain strengthening and anti-wilting decoction is to nourish the heart, nourish qi and blood, nourish the kidney and spleen, soothe the liver and relieve wind, open the body and increase wisdom, regulate the five internal organs, nourish nerve cells, and promote the normal operation of brain tissue function.

It is summarized on the basis of years of treatment of such diseases, using pure Chinese medicine formulas, syndrome differentiation treatment, symptomatic one person, compatibility with a large number of clinical experience on a series of symptoms caused by cerebellar atrophy, ataxia and atrophy diseases have a good effect, and through practical application to receive effective feedback, to bring help to patients; Gradually improve the recovery of oneself, with the naturalness of the ingredients, the uniqueness of the formula, the reliability of the effect, and the patient as a whole, so as to achieve the therapeutic effect.

Here are some TCM ways to do MND:

Acupuncture**: Acupuncture can regulate liver qi, relieve mental tension, reduce muscle tone, and reduce muscle spasms and pain. Commonly used acupuncture points include large vertebrae, liver yu, wind pool, etc.

Herbal medicine**: Traditional Chinese medicine can calm the liver and lower yang, dispel wind and phlegm, and have a good ** effect. Commonly used Chinese medicines include Bupleurum chinensis, Skullcap, Gastrodia, White Peony and so on.

Tuina Massage**: Tuina massage can improve local circulation and relieve muscle spasms and pain by regulating qi and blood, dispelling wind and cold, relaxing tendons and invigorating blood. Commonly used techniques include pinching, kneading, pushing, and holding.

This is also to follow the doctor's instructions and insist on going **.

Find a good Chinese medicine practitioner and follow the doctor's instructions to go to **.

Lower motor neurons, including the motor nuclei of cranial nerves, anterior horn cells of the spinal cord, and the nerve fibers they emit, are the last fluid-initiation pathways that receive impulses from all aspects of the cone, extrapyramidal, and cerebellar systems, and are the only pathways for impulses to reach skeletal muscle.

Its function is to combine these impulses and transmit them to the motor endplate through peripheral nerves, causing muscle contractions. Cranial nerves made up of axons emanating from the motor nuclei of cranial nerves directly reach the muscles innervated by their excitations. Axons emanating from motor cells in the anterior horn of the limb socks spinal cord pass through the anterior root, plexus, and peripheral nerves to reach the innervated muscles.

Traditional Chinese medicine does not have motor neuron disease, if the patient has motor neuron disease, there is no particularly effective method, such patients are unknown, and the effect is often not very good.

For these patients, the current ** is mainly remorse, symptomatic and supportive. If the patient has dysphagia and choking on water, nasogastric injection is necessary to prevent the patient from developing aspiration pneumonia and to ensure the patient's nutrition.

If the patient develops dyspnea or respiratory failure, endotracheal intubation or tracheostomy is usually required, and a noninvasive or invasive ventilator is required to assist ventilation**. Patients with motor neuron disease should pay attention to the following aspects: first, develop good living habits; second, strengthen exercises, such as chest expansion exercises, brisk walking, etc.; Third, pay attention to your diet and eat more high-protein foods, such as soybeans, fish, shrimp, etc.; Fourth, drink plenty of water; Fifth, prevent infections, such as respiratory tract infections and urinary tract infections; Motor neuron disease can be broadly divided into four categories, amyotrophic lateral sclerosis, progressive muscle atrophy, progressive bulbar palsy, and primary lateral sclerosis, of which amyotrophic lateral sclerosis is the most common.

The best way to treat motor neuron disease is as follows:

1. Drugs**: anti-excitant amino acid toxic drugs can be used to delay the development of early diseases, and muscle relaxants, antioxidants, etc. can reduce patients' joint contractures, joint stiffness, drooling and other symptoms;

2. Oxygen therapy: For patients with respiratory weakness, oxygen therapy can be carried out through a simple home ventilator to reduce the symptoms of dyspnea or respiratory failure;

3. Surgery**: If the patient has swallowing dysfunction, the gastric tube can be indwelled in the short term, and the gastrostomy can be performed in the long term;

4. Psychology**: Psychological assessment and psychological counseling can help patients understand and face diseases.

The specific medication should be combined with clinical practice, and the doctor's face-to-face guidance shall prevail.

First, the method.

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.

2. Nursing methods.

1. Daily care.

When the patient has a large amount of phlegm, nebulized inhalation and phlegm-reducing drugs can be given. When the patient has a lot of saliva, the patient may be given a small amount of antihistamine with medication**. When the patient is depressed, in a bad mood, and may have a tendency to depress, the patient should be given antidepressant in a timely manner.

2. Dietary care.

Patients also need to take care of their diet. The patient's diet needs to be balanced. When the patient has difficulty swallowing, try to adjust and change the diet, let the patient eat more soft food, semi-liquid food, etc., and also adopt a high-protein and high-calorie diet to ensure the patient's nutritional intake.

In addition, patients should avoid tobacco and alcohol.

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.

Motor neuron disease mainly relies on drugs ** and symptomatic **.

Drugs**. 1.Riluzole: taken continuously for 12 to 18 months, it can delay disease progression and prolong the survival of patients with progressive bulbar palsy.

2.Other medications: Your doctor may also choose prednisone, cyclophosphamide, neurotrophic factor, etc.

Symptomatic**. 1.Complications and accompanying symptoms such as swallowing, breathing, articulation, spasticity, pain, nutritional disorders**.

2.People with dysphagia are intubated and fed through a tube.

3.People with respiratory failure cut their trachea if necessary and use a ventilator to assist in breathing.

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.