I believe that every parent hopes that their children can be healthy, beautiful, rich, and can become a useful person to society. If, let's choose only one of these, I believe that all people will choose health. Because only health is the premise of all this, without health, everything is so illusory.
However, there is such a child, she has a unique appearance, but she does not have a healthy body.
She has a nice name called "Lan nini".
Looking at the short video, five-year-old Lan nini, fair skin, big eyes sparkling, especially cute. God must have carved her in his making. However, for this girl who looks as cute as art, God forgot to give her health!
Lan Nini's father and mother are free love, and they are also very loving after marriage. Because both people like girls, they want to have a cute and beautiful girl. After they learned the news of their pregnancy, they began to look forward to a better future, imagining that in the future, with their lovely children, a family of three could often travel and play together.
When she was pregnant with Lan Nini, Nini's mother was also very happy. Unlike many pregnant women who have severe pregnancy reactions, Nini is particularly well-behaved in her mother's belly. As if I knew that my mother was hurting, I never made my mother uncomfortable. It's not like some babies like to kick their mother's stomach and play. Nini, as if she was afraid of hurting her mother, never kicked her mother.
In fact, if it is an experienced parent, at this time, you should be vigilant. The fetus is in the mother's belly, too quiet, and may not be a good thing. If there is a similar situation, you should go to the hospital as soon as possible.
And when Nini's mother told Nini's father about the child's special quiet and worrying things, Nini's father did not pay enough attention because he was also inexperienced. Nini's father also felt that this must be a girl, not yet born, so well-behaved and sensible. And he has been looking forward to having a sweet little cotton jacket.
To their surprise, on the day of childbirth, when they saw the child held by the nurse, it was really a beautiful, lovely daughter, and they couldn't keep their mouths shut. I felt that heaven must have heard their voices, so I specially gave them a sweet daughter.
And Nini looks very beautiful, big eyes, long eyelashes, let people look at it will feel pity. Nini's father would often hold Nini in her swaddling and sigh:
"You are really God's reward for Mom and Dad."
In addition to having an angelic face, Lan nini did not cry or make trouble. When other children cry at night and disturb their parents. Nini was always quietly watching everything in front of her. As if afraid I would tire my mother. Nini's mother always praised outsiders, "Don't look at my nini for only a few months, but she is already very sensible." ”
It is also because there is no experience with the baby, Nini's parents mistakenly believe that Nini's too quiet, because she is born well-behaved and sensible, but what is the truth?
It wasn't until Lanni was six months old that Nini's parents began to feel that something was wrong. Is this kid a little too quiet? The child never seemed to cry or speak.
So, they quickly took Nini to the hospital for a check-up. They were surprised by the results of the examination. The doctor told them that the reason why Nini did not cry or make trouble was not because she was naturally well-behaved, but because she suffered from a "neurodegenerative disease". This is an extremely rare disease, and the probability of developing this disease is only one in 100,000, so that there are very few cases that can be used as a reference for hospitals.
Nini's father asked the doctor if there were any other symptoms of this disease besides not being able to speak. If it is just that they can't speak, like many deaf and mute children, Nini's parents seem to be acceptable. After all, such children are not in the minority.
But the doctor's answer made Nini's parents instantly fall to the bottom. The doctor said:
"Nerve regression will gradually degrade the performance of various organs of the body, and the symptoms are not only the inability to speak, the body will always degenerate, until it degenerates into a vegetative person."
On the way back, Nini's parents couldn't say a word. Until she returned home, Nini's mother looked at her lovely daughter, and this lovely life was going to gradually degenerate from their eyes until it was motionless. How did this make her accept it? She began to hold Nini and cry, "Why is there such a low probability that it happened to us?" My bitter Nini. Mom is willing to listen to you noisy every day, as long as you are healthy! "It turns out that behind the so-called well-behaved, it is all sad.
Nini's father's heart is also very unpleasant, the doctor said that this disease is a congenital genetic disease. If they can do a health check before they get married, it's possible to get it tested. But now it was too late to say anything, and there was no going back.
It can be seen that premarital examination is very necessary. Not only responsible for yourself, but also for the next generation. After all, health is the 1 in front of all zeros, and without the health 1, everything will be zero.
Lan nini's disease is too rare to be cured with money. Even the hospitals have very little information about the disease. And each person has its own special place, so it also brings great difficulties to the treatment.
Nini's father and mother, all day long looking at Nini in the cradle, sighing and worrying, but there was no way. Ever since she returned from the hospital, Nini's mother has been afraid to go out and face others. She didn't know how to respond to other people's concerns about Nini's condition. Tell them that my children will slowly degenerate until they become vegetative? In this case, she said not to export. Because, in her heart, there was still a glimmer of hope for Nini's condition that seemed unrealistic.
After countless long nights, Lanni's father decided that he could not complain like this anymore. Even if there is only one thousandth, one thousandth of hope, they must work for it. Although doctors have said that the possibility of a cure is almost zero. Even so, they have to "know what they can't do, and do it." At the very least, what they have to do for their beloved daughter.
Crying at home every day is not a good idea after all. Doing so is not half beneficial to the child. So, they began to seriously teach Nini to walk and play with Nini. Hopefully Nini can grow up slowly like a normal child.
In this way, under the careful care of her parents, Lan Nini slowly grew up, and she could even walk and run like other children. In the bright sunshine, Nini played happily, no different from ordinary children.
There are well-meaning people who advise Nini's parents that they can have another child. And they said that they only wanted to stay by Nini's side and give all their love to Nini.
While accompanying the child, he sought medical treatment. As long as you hear about where there is a possibility of a cure for the drug, no matter how far away and how expensive, you must buy it back. As a result, their savings are slowly being spent. The family had a very difficult time. Nini's parents do not have a high salary, in addition to daily expenses, the rest of the money is for the child's treatment. Even after giving everything away, Nini's illness still did not get better.
At the time of the rise of short videos, Nini's mother also registered an account for the cute little Nini, named "Lannini is earth". They want Nini to stay on Earth all the time, to stay with them, to be a carefree little angel. When Nini's mother posted Nini's photo to the Internet, the original intention was only to record Nini's growth, but she did not expect that Lan Nini was unexpectedly popular because of her beautiful looks. At first, people only paid attention to Nini's cute appearance like an angel, but later got the story behind Nini. Netizens then referred to Nini as an "angel who fell into the mortal world".
With more and more people paying attention, there are also many caring netizens who have given Nini more love and support. Some people send clothes to Nini, some people donate money for Nini, and some people try to find ways to inquire about the success stories of such genetic diseases.
In short, Nini and her family felt the warmth of the world, and because of this, they survived a lot of difficulties. After unremitting efforts to treat, Nini's condition was finally alleviated. Emotions slowly became richer, and outsiders could understand her communication.
What's even more surprising is that when Nini was five years old, she finally called out clearly, "Mom." This sudden surprise made my mother, who had been waiting for four years, cry with joy. But the heartache is that's all. It's a fact that the girl can't speak at 5 years old.
I believe that there will be more loving netizens who pay attention to this little life and pay attention to this family. Looking forward to the upgrading of medical technology, it can make Xiao Nini recover as soon as possible.