Female college students are unfortunately suffering from lupus erythematosus "Talking" encouraging her to return to the campus

(Correspondent Liu Shanshan) The 20 -year -old female college student unfortunately suffered from lupus erythematosus and needed to be treated by drugs for a long time. The torture of the illness made her lose her confidence in her life several times. While actively treating the medical staff of the Department of Rheumatology and Immunology of Wuhan Central Hospital, she continued to encourage her through "talk" and extended her help to donate to her confidence in defeating the disease.

The 20 -year -old Xiaohua (pseudonym) is a college student who reluctantly maintains his life by his parents. At the end of last year, because of physical discomfort, she was found to have systemic lupus erythematosus in a hospital. This disease was also called "immortal cancer" and needed long -term medication. Suddenly suffering from serious illness, Xiaohua and her parents were deeply hit, and they also worsened this poor family. Fortunately, after treatment, her condition was controlled. However, in February this year, Xiaohua suddenly had symptoms such as nausea and vomiting, and was sent to Wuhan Central Hospital for treatment by his family. After careful assessment, Fang Yan, deputy chief physician of the Department of Rheumatology, judged that the symptoms of digestive tract were related to lupus erythematosus. At the same time, she also had lupus nephritis, and her condition was more serious.

Chen Wenli, director of the Department of Rheumatology, discussed with the expert team and formulated a detailed treatment plan for her. During the hospitalization, Dr. Fang learned that since she knew this disease, she had a lot of psychological pressure, and her mood was not good every day. She dared not go to school to school, fearing that her classmates laughed at her. Dr. Fang gives comfort and encouragement every time the room is inspected, and popularized the knowledge of lupus erythematosus to her, telling her that the disease is not as terrible as imagined. As long as the treatment and regular review are standardized, they can learn and live like normal people. Under the patience of the doctor, Xiaohua gradually met and accepted the disease and returned to school to study again.

However, at the end of August this year, Xiaohua's condition recurred again, and many red rashes appeared on his face, and fungal infections appeared. Due to the serious condition of this time, the effect of conventional treatment is not ideal for her. Finally, the doctor decided to use a new treatment method -immunoaged treatment to quickly remove the antibody in the patient's body, reduce the concentration of the antibody, and reduce the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin and reduce the skin and the skin. Important organs damage.

Because long -term medication is a big burden for this poor family, Xiaohua once wanted to give up treatment. After learning about her family situation, the departmental medical staff launched a love donation in the WeChat group and filled the donation of 1,3300 yuan into her hospitalization fee. Xiaohua and his family were very moved by medical staff. After comprehensive treatment, Xiaohua's condition gradually stabilized. Before discharged, Fang Yan, the deputy chief physician, encouraged her: "Before the lupus erythematosus was called the disease of the" incurable disease ", but now with the improvement of the level of diagnosis and treatment, the efficacy of the systemic lupus erythematosus greatly improved. There are also many patients who have been treated with regular systems and successfully married and have children after the condition control. In fact, sickness is not terrible. The most terrible thing is the mentality. As long as you are actively facing the disease and you are optimistic about life, there will be hope. "

Chen Wenli, director of the Rheumatology Department of the hospital, introduced that lupus erythematosus is a kind of autoimmune disease that affects multi -organ and multi -system. Anemia, renal failure, pulmonary hemorrhage, cerebral infarction and other body damage and system damage, which is endangered. Because the pathogenesis of lupus erythematosus is unknown, it cannot be performed. At present, it can only be controlled by drugs.

Experts remind that patients with erythema rash, joint pain, anemia, oral ulcers, foamuria and other symptoms must go to the hospital for examination in time to exclude whether it is an immune disease. Patients with lupus erythematosus must be treated early, follow the doctor's instructions, and go to the hospital to review regularly to prevent the disease from worsening the danger of life.

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