The story of 17-year-old Florain Nalugon is becoming more and more famous on the Internet. The girl is sick with a rare genetic disease, but she does not lose her presence of mind and hope for healing. Reedus talks about this.
Florain has a congenital skin disease - lamellar ichthyosis. Because of this ailment, the girl's skin coarsens, becomes like scales, crumbles. This disease affects only 1 person in 600,000 living in the world, manifests itself from the first days of a child's life and causes, first of all, not physical, but moral suffering.
Parents told little Florain that she was born a fish and that is why she has such a skin. However, peers were not so soft-hearted and called the girl "snake", constantly teased her. Because of this, the family had to move to another city, but there the situation repeated itself.
According to Florain, only her parents give her the strength to hold on. And the girl is also singing - she started doing it in order to earn money for the examination. The Spanish doctors who have learned the story of Florain want to try the operation and cure the girl. And now she is full of hope:
"I am very excited to hear that there is a cure for my illness! I will study, get a good job and prove to all the people who laughed at me that I also have a chance to be like them."
