The Blonde Bikini Bombshell: Whatever Happened to Bo Derek?

Bo Derek is a treasured memory for children of the 1970s. She was one of the most stunning bombshells of her era, with her signature blonde hair, flaming blue eyes, and braided hairstyles that dispelled any negative connotations associated with them. Many people have been curious in her life since her brief period of stardom, like where she ended up, why she quit acting, and what her current circumstances are. Let’s see what Bo is getting up to these days.

The Early Years of Bo Derek

Mary Cathleen Collins was born in Long Beach, California, on November 20, 1956, before she became known as Bo Derek. Mary was raised by working-class parents in a typical American household. Her father worked as a sales executive, while her mother was a cosmetics artist. Mary had two areas of great interest when she was a teenager. She was first and foremost an avid horsewoman because she loved horses. She would compete in many events, proudly showcasing her talents. She also cherished acting. To improve those abilities, she decided to take acting classes.

Bo appeared in the movie Orca (1977). In this Jaws-esque film, a massive killer whale was shown biting off her leg. Her actual rise to prominence, meanwhile, was largely attributed to Blake Edwards’ 1979 picture “10.” It was at this point that her signature blond braided hair started to stand out. She didn’t go on a career of appearing in action-packed, daring movies after this one. Among them were the films “Tarzan, The Ape Man” from 1981, “Bolero” from 1984, and “Ghosts Can’t Do It” from 1990.

When Bo was just 16 years old, she met the director John Derek, who would become her husband. She was wed to Linda Evans at the time. They only started dating a few years later. But since Bo was still a minor, they had to travel to Mexico and Europe to get away from the harsh American laws.

https://www.instagram.com/p/B97MTGUHyY8/?utm_source=ig_embed&ig_rid=9a5cc36b-d802-42ae-b828-276f2819d123

“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.

© A True Story / Youtube

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.

© A True Story / Youtube

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.

© A True Story / Youtube

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.

Related Posts

Be the first to comment

Leave a Reply

Your email address will not be published.


*