An innocent gender reveal party swiftly descended into chaos. Luckily, my future mother-in-law was ready for the spectacle. When I discovered the rationale behind the last-minute dress requirement, I was taken aback and indignant.
Hello, my name is Tammy, and I’m thirty-one years old. Dean is thirty-two. This has to do with my fiancé’s family’s massive betrayal, which inspired me to pursue retribution.
For his first child, my future brother-in-law, Sam, planned a gender reveal party. Ignoring the warning signs, Dean and I accepted the invitation. It was strange that the invitation asked guests to bring presents, including medium diapers and something for the parents. We were told everyone had to wear white one week prior to the event. I bought a white jumpsuit with reluctance.
There was a nervous atmosphere at the celebration. Enthusiastically, Sam and Berta interacted with each other. Everyone was covered in pink and blue paint as it suddenly exploded in showers. The white clothing code, we discovered, was to sabotage our ensembles for their own entertainment.
The guests were furious, but Berta and Sam chuckled. Sam’s mother stepped in after noticing the shock. Instead of the destroyed garments, she gave them gift cards in an envelope. She was responding to the disrespect in this way.
His mother reprimanded Sam and Berta, teaching them a valuable lesson in decency and thoughtfulness. My soiled jumpsuit served as a visual reminder of how careless behavior can be as Dean and I departed, transforming a carefree celebration into a meaningful life lesson.
“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.”
© 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.
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