People all over the world, regardless of age or social background, pay attention to things that often influence how we are perceived. Shilah Madison and her parents decided to fight this attitude. All because of a rare disease the girl had.
She turned “unbrushed hair syndrome” into an advantage. She won the hearts of Internet users
Fourteen years ago, Shilah appeared in the world and immediately stole the hearts of Internet users thanks to her lush hair. Unusual, fluffy hair became hers. After some time, it turned out that the problems with taming the hairstyle had a genetic basis. She and her parents decided not to worry and turn the unkempt hair syndrome into an asset.
What exactly is “unkempt hair syndrome”? This disease does not occur very often
Uncombed hair syndrome, also known as limp hair or hypotrichosis simplex, is a genetic disease characterized by atypical hair structure and growth. People affected by this condition usually have it rare, weak and . Additionally, they can be difficult to style and maintain. Interestingly, owners of such strands most often boast light blonde hairstyles with a silver tint.
What does a girl with “unkempt hair syndrome” look like today? It still attracts attention
Currently, as a fourteen-year-old, Shilah actively promotes positive body image and self-confidence on social media profiles. Today she also knows how to properly take care of her hair.
Specialist care is provided by an expert in the field of curly hair care for people with dark skin. She is also conscious about her care, e.g. she sleeps on silk-covered pillows and lets her hair dry naturally, without using a hair dryer.
Source: Gazeta

Paul is a talented author and journalist with a passion for entertainment and general news. He currently works as a writer at the 247 News Agency, where he has established herself as a respected voice in the industry.