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.
Michael Strahan’s Daughter Reveals Heartbreaking Brain Cancer Struggle!
Michael Strahan’s daughter, Isabella, recently talked openly about her ongoing fight with brain cancer. In a heartfelt video on her YouTube channel called “Vlog 8: Recovering from Chemo at home,” the brave 20-year-old described the intense physical pain she’s going through during her treatment.
Isabella explained how agonizing the pain is, comparing it to a “heart attack.” She talked about trying to ease her headache by using an ice pack on her newly shaved head. She honestly shared, “Everything hurts,” and mentioned how her eyes, mouth, and jaw feel strained.
Isabella bravely shared about the intense pain she’s experiencing. She described her eyes feeling strained and painful when she looks to the sides. She compared the discomfort in her mouth to having all her teeth pulled out without replacements, saying even her jaw and tongue hurt when she drinks water.
Isabella admitted she would rather have radiation or brain surgery than endure chemotherapy because of the extreme pain it causes her. She called this journey the toughest and longest she’s faced, expressing worries about possible complications like heart pain, vision loss, or tooth decay.
Despite these challenges, Isabella is grateful to be home and sleeping in her own bed after being in the hospital. While she felt safe there, she finds comfort in familiar surroundings. Her vlog also showed moments from her hospital stay and special times with her father, Michael Strahan, and her twin sister, Sophia.
Isabella shared this update after she and her father talked about her illness on Good Morning America. She explained how she first noticed headaches and feeling sick, but didn’t worry until she woke up one day throwing up blood. Doctors later found out she had a serious brain tumor called a medulloblastoma. Michael Strahan was away from Good Morning America for more than three weeks because of “personal family matters,” though he didn’t say exactly what was happening.
Even with all these challenges, Isabella is staying strong. She finished her last round of radiation treatment in January after freezing her eggs because of her illness. Our thoughts are with Isabella and her family during this difficult time.
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