Xiaofang was born in September 2012 into a single parent family. She suffers from congenital anhidrosis (sweat glands produce little to no sweat) due to a genetic defect. There were three girls in the family – the eldest sister died of the same disease, and her second sister was given to others for adoption due to illness when she was young. Xiaofang’s parents are divorced, and Xiaofang currently lives with her father. The father spent all his savings to treat his children. He works in a vegetable greenhouse to earn medical expenses for Xiaofang and searches for treatment options. Xiaofang is in poor health and her legs are severely deformed. Although she cannot go to school, she is a sweet, quiet little girl who often helps her father with work as much as possible.
We hope to find suitable diagnosis and treatment resources for Xiaofang and alleviate the pain and stress she must deal with.
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