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
Heartbreaking Tragedy: 18-Year-Old Dies Just Weeks After Collapsing at Graduation!
A sad event has happened in a community recently. An 18-year-old girl named Sienna Stewart passed away unexpectedly at her high school graduation ceremony.
Sienna had a heart transplant when she was very young, at just 8 years old. She had a condition called cardiomyopathy since she was 4 years old, which made her heart weak. The transplant helped her live a fairly normal life for 10 years, but earlier this year she started feeling unwell again.
Her mom, Saevon Chum, said Sienna had been having episodes where she would collapse. Tragically, one of these episodes happened during her graduation ceremony on May 23, 2024. Paramedics were already there trying to help when Saevon arrived.
The principal of Hiram High School asked for a moment to help Sienna when she collapsed. It was a very distressing moment for everyone there.
Sienna’s mom described how the ambulance was already on the scene when she arrived. This time, Sienna didn’t wake up after collapsing, which had never happened before.
The whole community is grieving for Sienna Stewart, remembering her as a young woman who faced health challenges with bravery.
Sienna woke up a few minutes later and decided she wanted to go to her graduation ceremony instead of going to the hospital.
“All she told me was, ‘I just want to graduate, I want to walk.’ That’s all she wanted, because she missed her prom earlier when she was in the hospital,” said her mom, Saevon.
Sadly, Sienna passed away on Wednesday, June 12, just a few weeks after getting her diploma.
“As a mom, you feel so proud because she fought through something that hurt her. You have to be proud. I was proud until the end,” Saevon said.
According to Sienna’s obituary, she had plans to go to college and study sonogram technology starting in the fall.
Rest in peace, Sienna Stewart.
Leave a Reply