The girl who looked like a doll is now 9 years old – This is her today

When baby Aira was born, her parents knew she was somewhat special. With her blonde hair and big blue eyes, Aira looked stunningly beautiful and many agreed that she resembled a doll.

Although she was still just a baby, her parents decided she should be part of commercials, so they took her to a number of modelling agencies, many of which were interested to work with her.

Almost overnight, photos of Aira flooded social media and people were convinced she wasn’t real but a photoshopped photo of a cute-looking toddler. But Aira was real, and she was dubbed one of the most beautiful girls in the world.

The girl who looked like a doll is now 9 years old – This is her today

When baby Aira was born, her parents knew she was somewhat special. With her blonde hair and big blue eyes, Aira looked stunningly beautiful and many agreed that she resembled a doll.

Although she was still just a baby, her parents decided she should be part of commercials, so they took her to a number of modelling agencies, many of which were interested to work with her.

Almost overnight, photos of Aira flooded social media and people were convinced she wasn’t real but a photoshopped photo of a cute-looking toddler. But Aira was real, and she was dubbed one of the most beautiful girls in the world.

Sadly, her engagements with modelling robbed her of her childhood and everything kids her age did. She didn’t attend kindergarten and was in front of a camera most of the time.

However, as she reached five years of age, modelling agencies were no longer interested in her as she started resembling any child out there. She wasn’t invited to photoshoots and fashion shows.

These days, Aira is nine years old, and she still gets modelling gigs, but it is very rare.

She is active on social media, but there are no photos of her from her early days when she was dubbed doll-girl.

“People Only Know Me as a Freak,” The Wolf Man Struggles to Find a Job Outside the Circus

Jesús Aceves has hypertrichosis, which makes his hair grow abundantly over his face and back. Because of his condition, he’s also known as The Wolf Man. But he’s tired of this alias and wants to live a normal life.

© A True Story / Youtube

Meet Jesús Aceves, a 55-year-old man born with a condition called hypertrichosis, which means he has abnormal hair growth over his body, especially his face. Although married with kids, Jesús isn’t fully happy with his living conditions. He says he and his family suffer discrimination. In an interview, one of his kids mentioned, “People call me names, and they even tell their kids not to be my friends.”

© Chuy, El hombre lobo / Chuy, The Wolf Man / Facebook

He worked in the circus all his life, traveling through several cities. But now, he’s tired of being seen as a freak. As a consequence of years on the road, he’s been known as The Wolf Man.

Back home and not in the circus anymore, he’s facing another challenge: finding a “normal” job. He needs to support his family since his wife works in temporary jobs.

© A True Story / Youtube

After several failed job interviews, he agreed to try something he had always avoided: shave his face. He relied on his family barber to transform him, even creating eyebrows and lashes.

The experience was difficult since the face is an extremely sensitive body area, but both he and his wife believed that simply by shaving, he would be able to find a job.

© A True Story / Youtube

Jesús did several interviews, and it’s confident that now he’ll find somewhere to work besides the circus. If this happens, he must shave his face every 2 days.

Although rare, some conditions aren’t impossible to have. Luckily, people find a way to overcome the difficulties a rare condition brings and strive in life. Hannah Tyre, for example, was born with osteogenesis imperfecta, meaning that her bones break very easily. But her love for makeup made her an internet influencer, reaching millions of followers. We hope that, by reaching the mainstream media, people with genetic diseases won’t suffer more discrimination.

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