What a girl with a rare genetic disease looks like, whom the specialists helped

What a girl with a rare genetic disease looks like, whom the specialists helped

 What a girl with a rare genetic disease looks like, whom the specialists helped

The heroine of our story is Ukrainian Victoria Komar. Until the age of 7, the girl grew up like all her peers, no different from them. But when a misfortune happened in their family — their close relative passed away, little Vika was impressed.

After this incident, her genetic disease was discovered. Initially, her back suffered and then her parents turned to specialists. A rather rare diagnosis was made — Albright’s syndrome. This disease affects women.

And from the background of stress, a hormonal failure occurred, as a result of which the facial bones began to grow. No one understood what to do with it, because the growth of bones did not stop, which caused incredible discomfort to the girl.

Despite everything, Vika tried to find a way out of this situation. She went to work in a kindergarten, the children just adore her. And then she decided to send an application to the programs «I am ashamed of my body.» There, the best specialists of Ukraine undertook a huge job.

First, her chin was corrected, then new teeth were inserted. Thus, the girl was able to chew food normally for the first time in many years. And they also prescribed special hormonal pills that block the production of hormones. These are expensive medicines, so charitable foundations help Victoria.

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