Supatra ‘Natty’ Susuphan, once known as ‘The World’s Hairiest Girl,’ has transformed her life. Natty, 17, from Bangkok, Thailand, battled Ambras Syndrome, causing excessive hair growth. Guinness World Records recognized her in 2010. She used laser treatments, but now shaves to maintain her look.
Natty found love and posted on social media: “You’re not just my first love, you’re the love of my life.” Ambras Syndrome was once misunderstood, leading to stigma. Natty faced teasing and cruel nicknames like ‘Wolf Girl’ and ‘Chewbacca’ in school. However, her family and friends supported her.
Natty’s perspective is inspiring. She said, “Being hairy makes me special.” Despite the teasing, she’s grown accustomed to her condition and hopes for a cure someday. Her journey highlights self-acceptance and the importance of a supportive network.
It’s a testament to resilience and redefining beauty on one’s terms.
“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.
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.
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.
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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