3 year old child is sick and mother is in debt for her treatment: my child will never give up.
Ji'nan times
a rainy night before the weekend, 3 year old Ji'nan doll Lee Lin Xi has a high fever. Mother Zhang Lan embraced him in the rain, and rushed from Jiyang to the East Hospital of the provincial hospital. She finally saved her child's life. This has not happened for the first time.
the first onset was suddenly
supplementation. The child had a fever and fainted
Zhang Lan said that Xiao Lin was still less than 1 years old when he was first sick. Because of the poor family conditions, in addition to the mother's milk in the last few months, Xiao Lin Xi basically did not eat good things, adults drink porridge every day, children also follow the drink, there is no oil.
Xiao Lin Xi grew to six months. Zhang Lan was worried about undernourishment and began to feed him egg yolk and mix it up in the porridge a day. One day, after eating a whole egg yolk, Xiao Lin Xi suddenly had a high fever. He cried in a strange way. He passed out on the way to the hospital.
Xiao Lin Xi rescued locally and then transferred to Ji'nan. After two weeks of screening, the condition was finally diagnosed: methylmalonic acidemia, once onset, easily fainting and myasthenia. If the treatment is not timely, it may die. And this disease is difficult to cure, once the disease occurs, it takes lifelong medication.
a family has embarked on a difficult road to seek medical advice from then on
4000 of each month's life-saving medicine. The family has borrowed about 200000 of his relatives by
to cure his son. Zhang Lan said.
Zhang Lan and her husband are ordinary farmers in the village of Xinshi Town, Jiyang county. The economic source of the family is the income of the husband to work in the city and the 10 mu of the family. If children want to live, they can not stop medicine for one day, or at least 4000 yuan a month. The father of his father didn't earn enough money for the milk powder, so we could only be cheeky enough to borrow it. Zhang Lan said.
in order to maintain life, Xiao Lin Xi has to infusion once a day, and also take betaine, vitamin B12, Sodium Bicarbonate Tablets, Levocarnitine Oral Solution and so on. A Levocarnitine Oral Solution costs 15 yuan, two drinks a day. The infusion of a needle a day, one 20 yuan. Betaine is a package of 20 yuan a day. Even taking the medicine on time every day, the condition is still worsening. Fever often occurs. Hospitalization expenses and drug fees are not small.
in order to cure his son, Zhang Lan's husband went to work in Xi'an, earning about 3000 yuan a month. Even so, it is still a drop in the bucket.
a lot of similar families chose to give up, but his mother said, "
he is my child. I can't give up his
in the pediatric ward of the East Hospital of Shangdong Province-owned Hospital, and the reporter saw the strange sick baby Li Linxi." He was 3 years old, but he was smaller than his peers and couldn't tell a whole word, but he always had a smile on his face, and it looked particularly pleasing.
because his father went to Xi'an, Xiao Lin Xi was admitted to hospital every time. The friend who lives in the next bed tells the reporter that the mother often holds the child and does not move for hours in a few hours, afraid to wake up the sleepy child. At night, she begged the people of the same house not to put out the light, because her son could be ill at any time, and she could not see the lights out. When she was eating, she always pulled the curtains. Once the curtain was not pulled up, I saw her eating steamed bread in boiling water.
the doctor told reporters that methylpropanicalacidemia, also known as methylmalonic aciduria, is an autosomal recessive inheritance, and the disease often occurs in children. Children are often drowsiness, growth and development, and repeated episodes of vomiting, dehydration, respiratory distress and low muscle tension, at any time there will be life risk. At present, there is no cure for this disease. The current treatment method is mainly based on drug maintenance. This disease is great for a family, both mentally and financially, which has led to many parents choosing to give up treatment.
however, Zhang Lan could not bear to give up his son's treatment. He is my child, and I can't give up him. I hope there will be miracles in the future to cure his disease thoroughly, even if there is only a glimmer of hope. As long as there is hope to cure my son's illness, I would rather they take my son to do the experiment.