Will myasthenia gravis recur Ask me, can severe muscle weakness be eradicated and not recur?

Myasthenia gravis has the phenomenon of ** after being cured, but the condition is generally not mild, if it has affected the cerebral spinal cord and has psychiatric symptoms, it will be cured due to the influence of its own family environment and living environment, but it can continue to be cured. In general, myasthenia gravis is caused by a decrease in the function of internal organs and a decrease in physical fitness (except for special external causes, such as radiation, etc.). After being cured, you must protect your body, strengthen your exercise more, have a normal work and rest time, and eat normally.

Myasthenia gravis is not a terminal disease, as long as it is regular**, the symptoms of most patients can be relieved. But the main problem is that myasthenia gravis has a rate of more than 40%, so the focus of the disease is on prevention. Clinical studies have found that the main causes of myasthenia gravis** are as follows:

Patients often fail to take their medications as prescribed for the following reasons:

1) Busy work, irregular daily life, poor self-care ability (such as the elderly or children), forgetfulness, superstitious thoughts (such as not taking medicine during the New Year's holidays), etc.;

2) After the clinical symptoms are completely relieved, the maintenance medication period, due to the long time of medication and the patient has no obvious muscle weakness symptoms, the paralyzing thoughts are generated, and the drug is stopped or reduced without authorization;

3) When obesity, gastric ulcer, etc. occur due to hormone application, the patient should reduce and stop the drug by himself;

4) Interrupt medication due to learning of other new** or misled by advertising travel doctors.

In view of the above situation, the following countermeasures can be taken:

1) Repeatedly emphasize to patients and their families that failure to take medication on time can cause the condition to be aggravated or even aggravated, so that they can understand the importance of taking medication.

2) During the maintenance period, the follow-up interval should be formulated according to the recovery of the condition. The time interval gradually increased from 1 month, 2 months, and 3 months to half a year and 1 year, and the whole course of treatment was followed up 5-6 times, and each follow-up visit was guided by the physician to add or decrease the dosage.

3) Do not change the drug at will, change the dosage, and do not interrupt the drug according to your own judgment. Patients can increase exercise appropriately, eat more fruits and vegetables, eat less starch and oil-rich foods, and take sucralfate and other gastric mucosal protectors to reduce hormonal growth. For those who are indeed intolerant due to greater intolerance, drug adjustment should be carried out under the guidance of a physician.

Many myasthenia gravis can be done, such as myasthenia gravis caused by thymus gland problems, and they recover well after surgery.

This disease can be ****. Yiling Hospital is good. The probability of this disease is extremely small.

Myasthenia gravis, can this disease be **not**? This disease can't be a**, especially severe myasthenia gravis, can this disease be **not**? This kind of disease can't be treated, especially if it's severe, it can only be maintained, that's good, so this disease is not so easy to treat, and it's basically impossible to get out.

In patients with myasthenia gravis, it is usually due to genetic factors or due to endocrine and thymoma factors. If myasthenia gravis is caused by thymoma, then thymectomy is possible for half of the patients, but most patients with myasthenia gravis are not able to. Patients can be treated with drugs**, which can effectively slow down the progression of the disease, and patients mainly use cholinesterase inhibitors, or hormones and immunosuppressants to alleviate clinical symptoms.

In addition, patients should also pay attention to some functional exercises, active or passive muscle exercises, which can effectively prevent muscle atrophy.

Adjust the five internal organs and restore the function of the spleen and spleen meridians.

Myasthenia gravis depends on the severity of the condition and individualization**, and some patients may be treated with pyridostigmine bromide**. Pyridostigmine bromide is indicated for ophthalmomy, bulbar and generalized myasthenia gravis. It should not ignore the adverse reactions when adjusting the dose and frequency of the drug, which mainly include salivation, tearing, sweating, abdominal pain, nausea, increased stool frequency, etc., and even muscle spasm, glucocorticoids can also be used.

Glucocorticoids as first-line** drugs for myasthenia gravis can include prednisone, hydroprednisone, methylhydroprednisone, ophthalmic, bulbar myasnia, and severe generalized myasthenia gravis. Older male patients are more satisfied, and patients with thymus enlargement and active cellular immune response before or after thymoma resection can also achieve certain results.

Myasthenia gravis can get worse and need to be prompted**.

Myasthenia gravis is an autoimmune disease that is a weakness of muscle contraction caused by impaired transmission of neuromuscular junctions. Myasthenia gravis is generally divided into ocular muscle shape, systemic type, acute severe type, delayed severe type, amyotrophic type, congenital and other types, patients may have ptosis, difficulty swallowing, hoarseness, some patients will also have difficulty raising their heads, weakness of limbs, dyspnea and other symptoms, because myasthenia gravis will gradually worsen, so it needs to be timely **, so as not to endanger life.

Patients with myasthenia gravis can take mycophenolate mofetil capsules, tacrolimus capsules, compound cyclophosphamide tablets and other drugs under the guidance of a doctor**, if the patient has a rapid deterioration, it is also necessary to improve by plasmapheresis, if the patient is myasthenia gravis caused by thymoma, thymectomy surgery is needed in time to avoid aggravation of symptoms. If the patient has thymic hyperplasia or general weakness, further treatment can also be done by thymus radiation**.

Patients should pay attention to the management of daily life and appropriately limit daily life.

Dysfunction of nerve-muscle junction transmission is an autoimmune disease of acetylcholine receptors on the postsynaptic membrane at the neuromuscular junction.

Food contamination and poisoning: A considerable proportion of patients get sick from eating unclean fried fritters, low-quality drinks contaminated with chemicals, and some are caused by patients eating mushrooms.

Viral infection: the disease is associated with immunocompromise and infection with the chronic disease virus of the thymus.

Mental factors: Excessive fatigue is caused by playing mahjong for a long time and playing computer games, so it is necessary to combine work and rest to maintain a comfortable mood.

Other factors: hyperthyroidism, autoimmune diseases, polymyositis, lupus erythematosus, etc.

It will lead to the aggravation of myasthenia gravis, so early detection and early use of Chinese muscle building and health decoction can reduce the weight of the patient, and it is safe and stable.

Various physiological, pathological or drug factors, such as neostigmine overdose, organophosphate pesticide poisoning and other reasons, lead to excessive accumulation of acetylcholine at the neuro-muscular junction, which continues to act on acetylcholine receptors, so that the postsynaptic membrane continues to depolarize, the repolarization process is blocked, the neuro-muscle junction is blocked, signal transmission is impaired, in addition to respiratory muscle paralysis symptoms such as dyspnea, there are also muscarinic poisoning symptoms and nicotinic poisoning symptoms, such as vomiting, abdominal pain, diarrhea, miosis, sweating, salivation, Increased tracheal secretions, slowed heart rate, muscle tremors, cramps, and a feeling of tightness, etc. The use of neostigmine can aggravate the symptoms of muscle weakness, and cholinesterase inhibitors should be discontinued, and the choline receptor blocker atropine

Hello, myasthenia gravis has some aggravating predisposing factors, so you must pay attention to it, usually there may be the following factors:

The first point is that some patients usually lead to aggravation of symptoms after infection, such as respiratory tract infection, urinary tract infection, etc., which can lead to obvious aggravation of muscle weakness symptoms.

Second, if the patient is usually anxious, depressed, mood swings, or has insomnia, it can also lead to aggravation of symptoms.

Third, there are also some drug-related factors that can aggravate the disease, such as aminoglycoside antibiotics, some sedative drugs, morphine, and some antiarrhythmic drugs can also cause symptoms to worsen.

Myasthenia gravis is an autoimmune disease that has a clinical feature that is sometimes good and sometimes bad. When the immune status is good, the symptoms of myasthenia gravis will also improve significantly. When the immune status is not good, the disease can easily ** or worsen.

Studies have found that patients with myasthenia gravis are prone to overwork** and are prone to aggravation when they have infections. Mental and emotional tension, anxiety, and insomnia are also a cause of **. Female patients:

Menstruation, pregnancy, and childbirth can all lead to exacerbations. Myasthenia gravis is susceptible to various factors, such as mood changes, overwork, infection, improper medication, etc.

Guidance: This disease is an autoimmune disease caused by dysfunction of transmission at the neuromuscular junction and can be treated with immunofolded preparations and thymectomy**.

Liu Quanpeng, Deputy Chief Physician of the Department of Impotence, Beijing Deshengmen Hospital of Traditional Chinese Medicine What are the causes of myasthenia gravis?

Myasthenia gravis is aggravated by many reasons, including irregular menstruation, colds, contraindicated medications, and overwork.

The causes of myasthenia gravis are divided into two categories: one is congenital hereditary, which is very rare and has nothing to do with autoimmunity; The second group is autoimmune diseases, which are the most common. The cause of the disease is not clear, but it is generally thought to be related to infection, drugs, and environmental factors. At the same time, 65% to 80% of patients with myasthenia gravis have thymic hyperplasia, and 10% to 20% have thymoma.

Myasthenia gravis is an autoimmune disease, and the specific pathogenesis is not particularly well understood. It is mainly because of the production of anti-acetylcholine antibodies in the body, which causes neuromuscular junction conduction dysfunction, which leads to some clinical symptoms of weakness and easy fatigue of skeletal muscle. In some cases, myasthenia gravis is due to other antibody abnormalities.

In conclusion, it is an autoimmune disease that can also be combined with other immune diseases. Therefore, the use of immunosuppressants, immunoglobulin and other drugs can be used**, or plasma exchange, thymectomy and other methods can be used to effectively alleviate this symptom.

Myasthenia gravis has a great impact Often chronic onset or subacute onset Scattered from one muscle group to other muscle groups Manifested as the affected skeletal muscles are extremely fatigued If the eye muscles are objectively present, the eyes and face droop If the pharyngeal muscles are affected, the speech is weak, it is difficult to swallow, Choking on drinking water, Chewing is weak, The neck muscles are weak, and the head cannot be raised, The limbs muscles are affected, and the symptoms are lack of energy, dizziness, swelling, dizziness, drowsiness, paresthesia, numbness or tingling, such as weakness in lifting the upper limbs, difficulty in going upstairs or easy to fall in the lower limbs, difficulty breathing when the intercostal muscles are involved, and the voice is small and weak These symptoms worsen in the afternoon or evening and after activity and decrease or disappear in the morning or with rest or anticholinesterase medications.

The appearance of myasthenia gravis can seriously affect the normal function of the body's muscles, causing a range of symptoms, which are as follows:

1. Levator superioris weakness will cause weakness in opening the eyes, fission of one or both eyes will also occur, and in severe cases, complete ptosis, affecting normal vision.

2. Weakness of eye muscles and speech muscles is manifested as weakness of eye movement, weakness of speech, hoarseness or unarticulation after speaking, and inability to express personal language normally.

3. Masticatory muscle weakness will cause masseter muscle atrophy, which is mainly manifested as bilateral asymmetry of the cheeks, and the lower jaw will be displaced to the affected side when the mouth is opened, and normal eating and swallowing actions cannot be carried out, which will cause obvious malnutrition in the later stage.

4. Respiratory muscle weakness leads to weak or absent thoracic breathing, and a ventilator is clinically necessary.

Myasthenia gravis can cause consequences such as difficulty breathing, difficulty swallowing, and limb weakness. The harm of myasthenia gravis will be reflected in various muscles, such as respiratory muscles, masticatory muscles, upper limb muscles, lower limb muscles, etc. 1. Respiratory muscles:

When myasthenia gravis is severe, it can affect the respiratory muscles, resulting in dyspnea, which can be life-threatening. 2. Masticatory muscles: Patients with myasthenia gravis do not have the strength to chew food, have difficulty swallowing food, and are easy to suffocate when drinking water.

3. Upper limb muscles: Patients with myasthenia gravis have weakness in the upper limb muscles, making it difficult to raise hands and stretch. 4. Lower limb muscles:

Patients with myasthenia gravis have weakness in the muscles of the lower limbs, difficulty walking, going up and down stairs, etc. It is recommended that patients with myasthenia gravis should go to the hospital in time, do relevant examinations, and formulate a reasonable plan after comprehensive evaluation under the guidance of doctors.

Psychological problems can occur, and even after the patient recovers, the psychological effects will continue to exist, manifested as anxiety, nervousness, irritability, etc., and some patients will experience insomnia, nightmares and other symptoms.

Lung damage is present. Although the disease** has been repaired, the alveoli are damaged and cannot work normally, which may affect the patient's lung function, and symptoms such as dyspnea may occur, which is a manifestation of decreased lung function.

It is accompanied by body aches and fatigue, severe sore throat, and significant cough and sputum production. Subsequently, the fever decreased, but there were still sore throat, cough, runny nose and other manifestations, and finally the physical symptoms were significantly improved.

Body aches, fatigue, sore throat symptoms continue to worsen, then the body temperature begins to drop, most body temperature can return to normal, some elderly people begin to have a runny nose, still cough, sputum and other symptoms, and then all physical symptoms have improved.