I am a patient with cerebellar atrophy, but it is not inherited in the family. It is a minority of idiopathic ones. It is a sudden genetic mutation, and it comes to me without warning.

I have heard the stories of other patients. I don’t know if this is fate. They all love sports, and I am no exception. My dream is a football player and my idol is Ronaldo. I want to imitate him, but by the age of 17. My life was suddenly rewritten that year. I originally thought that I would go to the youth army to test my feet when I was 18 years old. However, when I was 17 years old, I contracted this disease. All of a sudden, my goals and dreams that I have been working hard for in my life were lost. Hard to face...

Until now, I don’t know if it’s good or bad... The good is that I don’t have the symptoms of other patients, but the bad is that I don’t have balance. I didn’t expect people to lose their balance so badly. I dare not talk to other patients. Say, from their point of view, they think you just don’t have balance, it’s no big deal, we have to sit in a wheelchair...

But in fact, a lot of people's movements rely on balance, good but not good enough, bad and not yet...the disease is only helpless...The physical hardship of these two decades has passed, and now we can face calmly. Yes, it’s only the economic problem of life... It’s because I don’t have balance, and I can’t do it when I go out to work. I can’t get the benefits that other patients have applied for... I can only rely on others to help me in my life.

Alas: When the two ends do not reach the shore and the mood is not good, I thought about giving up... But no matter how difficult the road ahead in life, we must always face it... Life process may be difficult, as long as you keep going, you can still find a lot of sweetness and beauty. fruit.