Whenever I pass by the school, see the children running happily and sweating on the playground, and listen to the sound of reading in the classroom, Zhang Guangqiang's heart is full of sourness. "Who doesn't want their children to sit happily in the classroom and study, but I don't know if I can wait until the day my son goes to school." Zhang Guangqiang said sadly. The picture shows Zhang Guangqiang caring for his son in a hospital bed.
Zhang Guangqiang's son, Zhang Yiyang, suffered from congenital hemangioma, and when he was a few months old, some erythema appeared on his right side of his swollen face. When Xiao Yiyang was seven months old, xiao Yiyang's condition was even more serious, and Zhang Guangqiang rushed to Jinan Children's Hospital with his son for treatment, but the results were not satisfactory. Subsequently, Zhang Guangqiang took Xiao Yiyang to Jinan Hemangioma Hospital for more than a dozen sclerotherapy treatment, but still did not see any improvement. The picture shows a photo of Xiao Yiyang before he fell ill.
With the aggravation of the disease, the lump on Xiao Yiyang's face is getting bigger and bigger, and Zhang Guangqiang, who is eager to save his son, can only take his son everywhere to seek medical treatment. "In order to see my son, we have all been to the hospital. First went to Jinan Children's Hospital, Xuzhou Children's Hospital, Nanjing Children's Hospital, Nanjing Armed Police General Hospital, and then went to Zhengzhou Children's Hospital, Shanghai Fuda Hospital, and finally to Jinan Hemangioma Hospital. Zhang Guangqiang looked helpless when he said this.
In 2019, Xiao Yiyang was diagnosed with congenital hemangioma at Shanghai Jiao Tong University School of Medicine. Subsequently, although Xiao Yiyang has been actively receiving treatment, the effect is not ideal, and the lumps on his face are getting bigger and bigger, even ringing in his daily life. "Taking a child out is often noticed by a lot of people, there is that kind of curious look, there is also that kind of pity look, and more often it is the look of looking at him like a monster." As the father of the child, Zhang Guangqiang can't stop the tears from wetting his eyes whenever he thinks of these past experiences of his young son.
Zhang Guangqiang's parents are not in good health, and in order to treat their parents, the family has been in debt. Since Xiao Yiyang fell ill, Zhang Guangqiang's life at home has become even more strained. "The child's illness caught me off guard, and I could only ask relatives and friends again to borrow money. Later, my wife also divorced me because of emotional discord, and my wife's departure made me feel like an ice cave. Zhang Guangqiang said bitterly.
On June 4, 2021, under the advice of the doctor, Xiao Yiyang underwent the first major operation in his life - in the case of general anesthesia, the "head and face dilator implantation" surgery was performed, and the small child's scalp was placed with a dilator wider than the forehead. Looking at his son on the hospital bed after the operation, Zhang Guangqiang, a seven-foot boy, couldn't help but cry, he couldn't imagine how much pain his son had experienced. However, the expander on Xiao Yiyang's head was broken in just over three months, which meant that Xiao Yiyang had to experience great pain again. "When the doctor carried my son into the operating room, I cried so much that the whole building could hear me, and I was so distressed that I was dying." Speaking of this, Zhang Guangqiang's eyes were once again reddened.
Xiao Yiyang most wanted to go to the kindergarten, and he often asked his father when he would be able to carry his school bag and take the yellow school bus to the kindergarten like other children. Every time Zhang Guangqiang heard his son's words and looked at his expectant eyes, he could only tell him that he could cure his illness immediately, and if he was cured, he could go to school.
Several years of medical treatment, several major surgeries, the family breathless. Now the father and son are dependent on each other, although they are saddled with huge foreign debts, Zhang Guangqiang thinks that as long as his son can grow up healthily, he will work hard to earn money to make up for these holes. However, the ability of relatives and friends is limited, Zhang Guangqiang can make fewer and fewer phone calls, and the borrowed money is also less and less. Zhang Guangqiang said helplessly: "The pain is in the child's body, and the pain is in my heart." Watching my son being tormented by illness every day, my heart was like a knife. My son's surgery is imminent, but the cost of the operation has not yet been settled, so I can only ask the benevolent people to lend a helping hand, give my five-year-old child a glimmer of hope, and give the child a chance to go to school. ”
If you want to help this cute child, you can long press the identification QR code to view the project details to donate. If it cannot be recognized, you can save the two-dimensional code to the mobile phone album, open and scan, and select the two-dimensional code from the album to scan and identify. The project was initiated by the China Social Welfare Foundation 919 Major Illness Relief Project, and was launched in the Internet fundraising information platform "Waterdrop Public Welfare" designated by the Ministry of Civil Affairs, and was responsible for the review, implementation and information feedback of the project. The final interpretation of the project belongs to the China Social Welfare Foundation. For details, please pay attention to the "WaterDrop Public Welfare" platform dynamics. Supervision Phone: 4009-010-919.
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