“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

The Basketball Court Girl: Her Journey Unfolds at 21

“The Basketball Court Girl: A Fate Decided at 21”

Tsyan Hongyan’s story is one of perseverance and hope, serving as a powerful inspiration to people worldwide, especially those with disabilities. Her life demonstrates that no matter the challenges, it’s possible to achieve greatness.

Tsyan lost both of her legs at the age of four in a tragic car accident. Her family, unable to afford prosthetic legs, had to find a way for her to adapt. Initially, her parents carried her, but her grandfather came up with a creative solution: he cut a basketball in half and placed Tsyan inside it, giving her sticks to help her move around.

This unique method of mobility caught the attention of many after a video of Tsyan went viral on social media. She quickly became known around the world as “the basketball girl.”

Tsyan’s determination was nothing short of remarkable. Despite her disability, she found a way to get to school on her own using this improvised “basketball transport,” although the journey took her an hour instead of the typical seven minutes.

At the age of eight, the government stepped in to provide Tsyan with prosthetic legs. With these new legs, Tsyan was able to take her first real steps toward independence.

Her dream, however, extended beyond walking. Tsyan had a deep love for swimming, and with her new prosthetics, she was finally able to pursue it fully. Despite facing many challenges, she set her sights on competing in the Paralympics, a goal that took years of effort and determination to achieve. Her hard work paid off in 2016 when she fulfilled her dream of participating in the Paralympic Games.

Today, Tsyan Hongyan is a celebrated swimming champion, with numerous medals to her name and worldwide recognition for her achievements. Her story reminds us that with perseverance, anything is possible. If Tsyan could overcome her challenges and find success, anyone can.