Joy and sorrow, walking and talking, these ordinary people's easy things, but it is a distant dream of 5-year-old girl Lan nini.
Lan Nini, suffering from Kabuki syndrome, is a rare disease, a hundred thousand times the chance of descending on Lan Nini, this disease gave Nini an angelic appearance, big eyes and long eyelashes, exquisite facial features, beautiful and moving.
When you first see her, you will be surprised by Nini's beauty, but when you look closely, Nini's eyes are always distracted, and Nini is indifferent to the touch and shouting of the outside world, quietly living in her own world.
From the time Nini was still in her mother's belly, they were surprised by Nini's wenjing, compared to the naughtiness of other children in her mother's belly, Nini seemed particularly quiet, and Nini's birth made her parents who had always longed for girls happy and broken.
However, as Nini grew up, Nini's parents also slowly discovered Nini's abnormality, Nini was too well-behaved, did not react to her parents' call, her parents felt wrong, took her to the hospital for examination, the result made them very broken, because Nini was diagnosed with neurodegenerative disease with cerebral iron precipitation type 6 "genetic disease."
It is a rare genetic disorder caused by the recessive chromosome genes of the parents and is almost incurable. Children can't speak and don't have the ability to take care of themselves. As Nini grows up, the performance of various organs in her body will also deteriorate, and she will eventually become a vegetative person.
But Mom and Dad didn't give up and have been taking Nini to major hospitals for treatment for so many years. Electric shock and rehabilitation were essential things for Nini to grow up.
Under the active treatment of her parents, Nini was finally able to walk and run normally. Although the effect is not great, it can be seen that Nini is constantly getting better.
And the high cost of treatment has gradually consumed the family's savings, the family's life is very difficult, in the rise of short videos, Nini's mother registered a short video for her, the account called Lannini is the earth, the reason for this name, is that her parents hope that she can always stay on the earth, do carefree little angel.
Unexpectedly, because of Nini's high appearance, the account instantly became popular. At first, people just thought that Nini was a beautiful child, and after learning Nini's story, netizens' attention to her was not limited to her appearance, and they felt sad for Nini's encounter.
They spontaneously extended a helping hand, some people bought clothes for Nini, some people took the initiative to donate money, and some people inquired about the treatment experience of this type of genetic disease, hoping to find an early cure.
With the help of well-wishers, Nini was able to continue to heal smoothly. In the latest video, Nini's eyes have a lot of energy, and even after one treatment, she vaguely shouted her mother, Nini's parents cried with joy, and netizens also wet the corners of their eyes.
The heartache of the mother of a special child, I am afraid that no one can understand, fortunately, the medical development is changing rapidly, modern medical treatment is constantly improving, and we are also looking forward to seeing this little girl can have a day of being cured.