“Zhe Bingren” Dai Panfei: Reading University with Strong and Loving Mothers

"I must study. If I don't study, I become a waste person." He once said to his mother.

On the face of an adult, the child's small limbs are bent, with a ventilator.

He called Dai Panfei, who lives in Zhongdai Village, Tangxi Town, Licheng District, Jinhua, Zhejiang Province. He was born in 1990 and has progressive muscular dystrophy. This is a gradual muscle contraction as he grows older, and gradually improves his ability to move. It disappears until it completely loses the ability to take care of itself, and the patient is commonly known as “being the ice.”

Alive is a miracle

Listening to Dai Feifei’s mother, she said in February that he’s still fat and slim. He’s already 42 pounds. He’s not even 40 pounds before.

Dai Panfei once said that if he can live, it is already a miracle.

It turned out that shortly after birth, Dai Panfei was diagnosed with progressive muscular dystrophy. At that time, some doctors said that Dai Feifei was only 18 years old. Some people even persuaded the two months and the husband to throw the child.

But they chose to raise their children up and down. Dai Feifei’s life can't take care of himself. He wears bimonthly feeds for him every day, helps him to wash his face and comb his hair, and takes care of him like he did when he was a child. He never complains.

In order to treat his son's illness, Dai's everything stagnated in 1997. From that year on, the two-story house has no more furniture, and there is no indoor toilet.

Wearing two months did not have time to work, taking care of the son has occupied her full time. In order to heal the illness, Dai Bixiu took his son to Shenyang, Shijiazhuang, and Shanghai for medical treatment. He had never given up as long as she had a glimmer of hope.

“Now, it's only father who feeds our entire family at home. It's very hard.” As the sole source of income for the family, Dai Panfei, the father of a veterinarian, had to raise pigs and farms in order to make more money to make up for the family, but still Not enough to wear Pan Fei's treatment costs.

College student with mother coming out

"I must read. If I don't study, I become a waste person."

Dai Panfei missed the book, but he was a problem even if he walked. He needed to use a small bench to walk. Many children with this disease are no longer in school at the elementary school, but he has always been to the university with his own strength and his mother's love.

In order to support his son’s dream, Dai Bifei leaned back with a lean back to wear his own body. This back is 6 years, until Dai Panfei finished high school.

In this 6-year period, Dai Bingyi broke three bicycles.

Dai Panfei also did not disappoint his mother's hopes. He always ranked first in the high school era.

Although he was not very successful due to physical reasons at the 2010 college entrance examination, he still entered Taizhou University and became a student in computer science and technology. He is very eager to learn that he has already won a first-class scholarship at the university and a secondary school scholarship.

Dai Panfei once told reporters that he worshipped Hawking, a great scientist with only two fingers. "I know I can't move in the future. I'll learn computers and then use computers to do what I want."

In 2011, Dai Panfei was nominated as a "moving Taizhou" figure.

Now he will use Weibo to ask for help. With the help of students from Zhejiang Normal University, in July of this year, the micro film "The 23rd Spring" which actually recorded his and her mother's story was born.

Countless netizens were moved and they sent donations and blessings to Dai Panfei.

As long as the son is alive, some of his back is good.

"Climbing the fly and the tricuspid regurgitation, the heart is not good, breathing is a bit difficult. In February of this year, Chuangfei took the ventilator. It used to be good and it would be writing and walking. It is very difficult now." Dai Bishuang told reporters.

Dai Feifei is currently hospitalized for the treatment of progressive muscular dystrophy at the Shenyang PLA 463 Hospital.

"The doctor said it was late. I said no. My son will continue to live." If you wear two months, you are already choking.

“It is all children aged seven or eight, who are seven or eight years old. They are like climbing so big. There is no such thing as climbing the age of such a big age, and it is very rare for this disease to survive this age. "Dai Shuangyue said that his own wish is that his son is alive and his back is good."

Dai Shuangyue told reporters that the stem cell transplant Dai Panfei is currently doing once a year is now the third year. Progressive muscular dystrophy is currently not completely cured and can only relieve symptoms.

Dai Panfei asked for help on Weibo. "I just did three stem cell transplants. I spent only 55,000 yuan for only 10 days. My family is really unable to pay for the remaining 15,000 treatment fees. I begged Sina to help people who are good to help." I……"

Dai Biyue said that Dai Panfei’s “strike a pack of stem cells in the hospital would require more than 10,000 yuan. He has already played three packs and he has to play two packs. That 55,000 are donated by good-hearted people. Now there is no money to give the child any more. I am now only suffering from progressive muscular dystrophy, but also to go to Shanghai to treat tricuspid regurgitation. There is no rule of law for tricuspid regurgitation here.”

Dai Panfei is still full of nostalgia for the school. He also hopes that after graduating from college, he can return his parents to return to society. "He is now unable to walk at all, and he still wants to go to school." Bimonthly could no longer suppress his tears.

Attached:

If you are willing to help Dai Peifei, you can contact his mother for two months

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