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She Cried When They Called Her An Ape; Years Later Her TikTok Videos Have Gone Viral; Meet Kawana
May 2, 2021
In the outskirts of Sau Paolo Kawana a young girl of 22 years has been battling with a rare congenital disorder known as Barber– Say syndrome.
Barber say syndrome is a very rare conginental disorder associated with excess hair growth, fragile skin, eyelid deformities and an overly broad mouth. Kawana mostly has gum issues and she has had more than 20 surgeries on her mouth.
This condition so far has only 20 cases recorded in the whole wide world and Kawana is one of such people who has gathered the courage to show the world she' s not intimidated by her condition Growing up as a child was a difficult task for Kawana although she had the support of her family.
Kawana will spend hours in her room crying due to bullying by her classmates and peers and would often not understand why she of all people will look like this. Her father who' s late for now was her only motivation at that point.
The mindset of children when it comes to physical appearance is something else and they will not hesitate to make fun of you.
However now 22 year old Kawana is a strong lady whose a motivation to most. Despite her condition she makes very cool tiktok videos which has fast gone viral thus bringing her in an interview with truly.
One might ask how does she cope whiles going out.
Well kawana is an adult now and her mindset toward how people see her has totally changed. Before Covid the young lady always went out without anything covering her face although some people freak out after seeing her.
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