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Brothers and sisters suffer from rare diseases, and before the brother died, he asked his mother to let his sister live...

Xiaoling is from Huainan, Anhui Province, and was a former mother of two children. At the age of 20, she met her husband and had a son Xiaohan and a daughter Xiao rou after marriage. Although the couple are farmers and have no skills, they can live a carefree life by relying on their industrious hands.

In August 2018, her son Xiaohan, who had just turned 7 at the time, suddenly had a high fever, vomiting and a large number of nosebleeds, which frightened Xiaoling, and she quickly sent the child to the local hospital. But after a week of inspection, the fever slowly receded. However, the doctor found that Xiao Han had many bleeding spots on his body, and his face was very yellow, and he could not accurately judge the condition, so he suggested that they go to a higher-level hospital for treatment.

In the following months, Xiao Han's condition was not effectively controlled, and the frequency of nosebleeds and fevers became higher and higher. After several turns, Xiao Han was finally diagnosed with "Fan Kony anemia" in May 2019 at peking university people's hospital. This is a rare inherited blood system disease caused by genetic mutations, and a slight fall or small bump can endanger a child's life. The most effective treatment is a hematopoietic stem cell transplant, but it is expensive.

Brothers and sisters suffer from rare diseases, and before the brother died, he asked his mother to let his sister live...

At the same time, the doctor also told Xiaoling and his wife: "This disease is related to genetic factors, and your daughter may also have the possibility of getting sick, it is recommended to do a test to prevent it." Xiaoling and her husband did not hesitate, and then gave their daughter Xiaorou a genetic test, and the results showed that she also suffered from "Fan Kony anemia". Two thin medical certificates broke down the whole family at once. The two children often have bleeding spots and green spots on their bodies, and nosebleeds have become "commonplace", and if they are not treated, they are life-threatening at any time.

Brothers and sisters suffer from rare diseases, and before the brother died, he asked his mother to let his sister live...

In August 2020, his son Xiaohan successfully underwent a transplant after more than two months of preoperative preparation. More than 20 days later, Xiao Han was successfully discharged from the warehouse and was transferred to the general ward. Xiao Ling thought that her son was finally waiting for rebirth, but soon after, Xiao Han's body had a serious rejection reaction. After struggling tenaciously with the disease for more than 2 months, Xiao Han left his family on December 30, 2020 due to multiple organ failure. Before leaving, he took Xiao Ling's hand and said, "Mother, if I die, you must let my sister live, and I will also bless her in heaven." ”

Because of the torment of illness, Xiao Rou often said to Xiao Ling, "Mom, give up on me, I am not cured, I can go with my brother in the future, and my brother will not be lonely." Xiao Ling could only be silent after listening, and her heart was like a knife.

Brothers and sisters suffer from rare diseases, and before the brother died, he asked his mother to let his sister live...

Nowadays, in order to raise money to treat her daughter,The family works day and night, and wants to earn more medical expenses for the child, but this money is undoubtedly a drop in the bucket for Xiao Rou's treatment.

Video source: @Mammoth News

Source: Mammoth News, Micro Public Welfare Editor: Silent

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