, a "half-body boy" became the biggest highlight of the night.
The two communicated in the spotlight, imagining a bright and peaceful future.
"Half-body boy" conveys the best kindness to the world with his innocent smile.
"Nothing Is Impossible".
All kinds of media reports use this sentence to describe Mufta.
For Mufta personally, he prefers to describe himself with "incredible".
His growth experience is a heroic epic that does not bow to fate.
Mufta's mother was told by the doctor during her last examination before delivery that the child had congenital caudal degeneration syndrome, that is, she would lose her lower body at birth.
Even if you are born, the probability of a child living for 15 years is extremely low. What is more painful than this is that he will face endless treatment for his whole life.
This is like a bolt from the blue.
After relatives and friends learned about this, they came to comfort themselves and suggested that Mufta's parents give up the child.
The two of them thought about it over and over again, but the mother made a statement first: "We cannot give up this child. I will be his left leg in the future, and you will be his right leg!"
The father felt sorry for his wife, and he couldn't bear to give up his own flesh and blood easily, and firmly agreed.
On May 5, 2002, Mufta, who had only the upper body, was born.
His parents named him "Ghanim", which means "winner" in Arabic .
Since I became sensible, my parents began to train Mufta to walk with their hands.
Sometimes I can practice too much, and the child's tender hands are covered with blood blisters.
As a long time, Mufta, who was a little older, developed resistance and began to resist and train negatively.
The mother was so angry that she pulled him to the window to see a group of children outside chasing and playing on the court.
"Do you want to run freely like them? They are born to be able to do it. If you can't, you can only work several times or even dozens of times more than them!" After that, he stared at Xiao Mufta with tears in his eyes.
He later recalled, "I will never forget the look of my mother that day."
Since then, Mufta has trained harder than before, and has never complained again.
The difficult years have made him know how to cherish what he has.
In the early days of the student days, Mufta was full of strange eyes from his classmates.
Even so, my mother still encouraged him to communicate with the outside world.
"The world is beautiful, everything can happen" is what my mother often says to Mufta.
subtly, the boy kept trying to face the world with a smile.
He actively participates in various activities organized in the school and does not feel inferior at all because of his physical condition.
His optimism and tenacity gradually infected the people around him and gained admiration and kindness from teachers and classmates.
Today, in personal social media, Mufta always smiles in front of the camera.
For many years, this kind of struggle that is almost "stubborn" against life and setbacks has allowed Mufta to find his freedom and ambitions.
More and more people know his story and are infected by his spirit. Before the World Cup, his social media fans exceeded 3.3 million.
During the preparations for the 2022 Qatar World Cup , the organizing committee directly contacted Mufta and invited him to serve as the World Cup ambassador. Before he went on stage on the opening ceremony that night of the opening ceremony, he gave a thumbs up to the people he was traveling with, as if telling everyone: Everything will go well.
Now Mufta is 20 years old, he founded an ice cream company and became the youngest entrepreneur in Qatar .
When I was free, Mufta often wore shoes with his hands and chased on the green field with his friends with "normal figure".
Mufta has always been looking forward to one day to step onto the Paralympic arena. He is eager to prove to the world that physical disability does not mean "submission" to fate.
"Everyone has the right to pursue his dream and has ambitions for it." This is Mufta's understanding of dreams.
Looking back at the journey we came, Mufta is full of gratitude to those who have helped him.
hopes to pass on goodwill Mufta and his family to set up a charity association, purchase wheelchairs and donate them to children in need to help more people.
Mufta family has also personally written several books related to tail degeneration syndrome and distributed them for free in their area.
He wholeheartedly fulfills his charitable mission and shows to the world; people with disabilities can also realize their own life value.
He said: "For me, the moment when I see my dear parents proud of me means everything. This is my motivation and encourage me to continue. I will do my best to hope to see the spark in their eyes;
I learned a lot from my mother. She told me that life is beautiful and nothing is impossible. I want to tell people that everyone has the right to dream and have the ability to achieve success. My motivation comes first from God, then my family, friends, and my country. "
" They often say that things that cannot kill you will make you stronger. That's right, being born with disabilities has made me a strong person, and it has allowed me to show all the advantages of my character. "
Even if you don't have a healthy and complete body, as long as you have a bright and kind heart, you can still make the world better.
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