The tattooed “Black Alien” has difficulty finding work because of his appearance, see what he looked like before

Anthony claims that despite making significant changes, including removing his upper lip earlier this year, he feels he has only achieved 34 percent of his transformation goals.

For over a decade, Anthony has been engaging in extreme body modifications and taking risks, such as getting eyeball tattoos that temporarily compromise his vision. His quest for an extraordinary look led him to have both ears removed and his tongue surgically split.

To achieve his desired changes, Anthony has traveled the world and undergone medical procedures in countries where such changes are prohibited in France. Last year, he traveled to Spain to have his nose surgically removed. His face now has structured, defined lines, thanks to dermal implants that accentuate his cheekbones.

With a remarkable Instagram following of 718,000 under the pseudonym Black Alien Project, Anthony continues to captivate audiences with his tireless efforts to transform his appearance.

In a recent post, Anthony showed off his latest modification, a surgically altered “alien claw” with a fresh scar. He captioned the image, “Cultivating my inner peace.” His bold changes often elicit mixed reactions; some admire his bravery, others are skeptical.

One commenter described Anthony’s transformation as both disturbing and fascinating, expressing admiration despite not being able to take such a path himself. Another congratulated him on his progress, calling it “incredibly wonderful.”

Conversely, some critics oppose it, arguing that his modifications show a lack of respect for those who have lost limbs and are looking for ways to adapt.

Despite the mixed feedback, Anthony remains committed to his transformation journey, a passion he has had since his youth. In a 2017 interview with French newspaper Midi Libre, he shared: “During my time as a security guard, I realized that I was not living the life I wanted. At 24, I made the brave decision to leave everything behind and travel to Australia. It has become second nature for me to constantly keep an eye on and plan my future steps.”

“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.”

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.

Preview photo credit A True Story / Youtube

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