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
ROYAL TRAGEDY. William and Kate are in shock.
When the Prince and Princess of Wales bought pizza for mountain rescue workers, they met a man selling pizza and wrote a touching funeral speech for him.
Father of two Peter Morris, who was 47 years old, died of cancer in May, not long after Kate was told she had it.
On notepaper from Kensington Palace, Prince William wrote his wife Tracey a letter of condolence. When he died, it was read.
“I can’t even begin to imagine what a huge hole he will leave in your life,” he wrote. “My heart goes out to you and your family.”
“Catherine and I had a great time meeting Pete.”
“We know Pete was a very dedicated and well-liked member of the community because of how people have responded to his death.”
“I wanted you to know that you and your family are thinking about you right now.”
In April of last year, Kate and Wills bought 12 pizzas from Peter’s converted VW van for £127.50. Peter is from Ebbw Vale in South Wales.
They gave the Central Beacons Mountain Rescue Team a choice of pizzas while they were at Dowlais Rugby Club in Merthyr Tydfil. The pizzas were margarita, pepperoni, BBQ chicken, and goats cheese.
At the time, Peter said, “They were really nice.” When I was setting up the business, I never would have thought that one day I would work for the young king.
In 2016, Pete opened Little Dragon Pizza Van.
He had beaten esophageal cancer, but doctors found it in his adrenal gland and liver four months after he became a royal. He died in less than a year, but the business keeps going.
The letter from William will be framed for Pete’s daughters, who are eight and five years old.
Tracey, who is 40 years old, told The Sun, “It was a huge surprise.” I have no idea how they learned that Pete had died. Because Kate is getting help, it may have struck a chord with them.
“He talked about how normal they were.”
“Many people wrote to tell us they loved Pete, but the letter from William and Kate was the most lovely.”
William wrote his wife Tracey a letter of condolence on paper from Kensington Palace.
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