How does life unfold for a little British girl grappling with untangleable hair syndrome? Delve into this extraordinary journey to understand the challenges and triumphs she faces daily. Click the link to explore her remarkable story.
Uncombable hair syndrome is not known to everyone. This is not surprising, because only 100 people in the whole world can boast of such an anomaly of hair. One of the owners of an amazing zest in appearance is three-year-old British Leili Davis. What a girl looks like in everyday life and whether her hair attracts the attention of others, you will find out with us in the next couple of minutes.
Uncombable hair syndrome
Leili Davis is only 3 years old, and her blog is followed by almost three thousand Internet users. And you shouldn’t be surprised by such popularity. After all, the reason for this was the uncombable hair syndrome that nature endowed the young British woman with. As you can probably already notice, the girl has silver-blond hair that has a lot of volume. It is impossible to create a smooth hairstyle out of them. However, this does not apply to a bun or braided hair.
As Charlotte Davis, Laili’s mother, admits, she and her husband hoped that the situation with the girl’s hair would improve. However, over the past year, my hair has only lengthened, remaining not only silver-blond, but also just as dry. “She had her hair cut for the first time in February last year, although it looked quite unusual. Now we can braid our hair. But you can do this infrequently so as not to pull them too hard. The hair itself is incredibly fragile and can easily break , ” the woman shares in a conversation with reporters.
Despite such a curious highlight in her appearance , Leili has no problems with acceptance in society. Quite the contrary, in kindergarten the pupils incredibly admire the girl. At the same time, they came up with a corresponding nickname for her – Fluffy. “Other kids don’t react negatively to it. She is a very happy child, not shy and sociable.”
“I hope she thinks her quirk is cool.”
What’s interesting is that the parents of the three-year-old British girl themselves are ready to joke about the topic of uncombable hair syndrome. So, until recently they called their daughter Boris Johnson and even Albert Einstein. Charlotte Davis believes that in this way she will prepare the heiress for the comments and questions from society that will inevitably arise later.
“ I just want her to love her hair. After all, when she grows up, children around her will begin to comment on her appearance . Your job as a mom is to prepare your children for any situation. So I just hope she thinks her quirk is cool like I do.”
It is curious that such an anomaly was first mentioned back in 1912. Uncombable hair syndrome itself is not at all dangerous and is not associated with any other disorders. Such a zest in appearance can develop in infancy. And if some people lose their peculiarity in adolescence, others can live with it all their lives.
I wonder how you would feel about such a syndrome? Are there any such “dandelions” among your friends?
