She was born with an unusual congenital melanocytic nevus.
Winry, 14 months, was born with an unusual birthday occupying a quarter of a face.
She was born with an unusual congenital melanocytic nevus, or VMN, a disease that suffers about one out of every 50,000 children.
Nicole Lucas Hall, Winry’s mother, took advantage of social networks to express the beauty of her daughter in the hope of standardizing his birthmarks and other uglies.
Her goal is to make Winry always feel beautiful, so that when she becomes older, she is always pleasant and confident in herself.
Nicole, Winry’s mother, and her four-year-old son Asher say that they were puzzled and scared by their newborn child from the moment Winry met.
Vinceri has a little higher the risk of getting a melanoma.
Nicole, on the other hand, claims to control his skin care.
«Our main goal is his health and happiness».
Winry’s mother is more worried that her daughter is subjected to persecution when she becomes older than small health hazards.
And for this reason, she decided to start using a blog on social networks.
For example, Instagram to inform people about Winry’s condition.
Their daughter publishes cute pictures of Winry and Asher along with information and resources.
